Open Access Article
This Open Access Article is licensed under a
Creative Commons Attribution 3.0 Unported Licence

Chitosan/metal organic frameworks for environmental, energy, and bio-medical applications: a review

Akash Balakrishnan a, Meenu Mariam Jacob b, Nanditha Dayanandan b, Mahendra Chinthala *a, Muthamilselvi Ponnuchamy b, Dai-Viet N. Vo *c, Sowmya Appunni d and Adaikala Selvan Gajendhran e
aProcess Intensification Laboratory, Department of Chemical Engineering, National Institute of Technology, Rourkela, Odisha 769 008, India. E-mail: chinthalam@nitrkl.ac.in
bDepartment of Chemical Engineering, College of Engineering and Technology, SRM Institute of Science and Technology, Kattankulathur, 603 203 Tamil Nadu, India
cCenter of Excellence for Green Energy and Environmental Nanomaterials (CE@GrEEN), Nguyen Tat Thanh University, Ho Chi Minh City, Vietnam. E-mail: vndviet@ntt.edu.vn
dDepartment of Chemistry, KPR Institute of Engineering and Technology, Coimbatore, 641 047 Tamil Nadu, India
eDepartment of Biotechnology, Vinayaka Mission's Kirupananda Variyar Engineering College, Salem, 636 308 Tamil Nadu, India

Received 14th July 2023 , Accepted 13th October 2023

First published on 8th November 2023


Abstract

Chitosan/metal–organic frameworks (CS/MOFs) are versatile materials fabricated by conjugating the chitosan (CS) material with metal–organic frameworks (MOFs). The CS/MOFs demonstrated phenomenal features such as higher surface area, porosity, non-toxicity, environmental safety, and ability to form different structures, making them suitable for diverse applications in adsorption, catalysis, membrane separation, supercapacitors, batteries, fuel cells, sensing, food packaging, and biomedical applications, including drug delivery. The different preparation routes for fabricating CS/MOFs are elucidated in detail. The CS/MOFs mostly remove emerging pollutants via adsorption and membrane separation. However, CS/MOFs are less explored in supercapacitors, fuel cells, and food packaging. This review highlights the preparation, characteristics, and applications of CS/MOFs for energy, environmental and bio-medical applications. The advantages, disadvantages, and perspectives are also elaborated. The following review is expected to be a useful guide for scientists working on CS/MOFs.


image file: d3ma00413a-p1.tif

Akash Balakrishnan

Akash Balakrishnan received his master's degree in Chemical Engineering in 2020 from the SRM Institute of Science and Technology, Chennai, India. Currently, he is pursuing a PhD degree in the Department of Chemical Engineering, National Institute of Technology, Rourkela, India under the supervision of Prof. Mahendra Chinthala. He is working on the development of 3D biopolymer-supported photocatalysts for energy and environmental remediation. His research includes photocatalytic degradation of organic pollutants, production of chemicals, biopolymers and process intensification.

image file: d3ma00413a-p2.tif

Meenu Mariam Jacob

Meenu Mariam Jacob completed her Master's in Chemical Engineering from SRM Institute of Science and Technology, Chennai, India. She is currently pursuing her PhD in Chemical Engineering under the guidance of Dr P. Muthamilselvi in the Department of Chemical Engineering, SRM Institute of Science and Technology, Chennai, India. She is working on wastewater treatment using adsorption and membrane technologies. Her research interests include wastewater treatment, adsorption, membrane, detection, modelling, and carbon-based materials.

image file: d3ma00413a-p3.tif

Nanditha Dayanandan

Dr Nanditha Dayanandan received her doctoral degree in Chemical Engineering from SRM Institute of Science and Technology, Chennai, India. Currently, she is working as an Assistant Professor in the same department at the SRM Institute of Science and Technology, Chennai, India. Her research interests include membrane technology, membrane distillation, polymeric nanocomposites and wastewater remediation.

image file: d3ma00413a-p4.tif

Mahendra Chinthala

Dr Mahendra Chinthala obtained his doctoral degree in Engineering Sciences from Homi Bhabha National Institute (Indira Gandhi Centre for Atomic Research), Kalpakkam, India in 2016. He is currently working as an Assistant Professor and leading the Process Intensification laboratory at the Department of Chemical Engineering, National Institute of Technology, Rourkela, India. His research interest includes electrodialysis, electrochemical separations, ion exchange, adsorption; advanced oxidation processes, gasification of biomass, and chemical process simulation using ASPEN PLUS.

image file: d3ma00413a-p5.tif

Muthamilselvi Ponnuchamy

Dr Muthamilselvi Ponnuchamy completed her PhD from SRM Institute of Science and Technology, Chennai, India in 2016. Currently, she is working as an Assistant Professor in the Department of Chemical Engineering, SRM Institute of Science and Technology, Chennai, India. Her research interests include wastewater treatment, membrane technology, and utilization of waste to wealth and process control.

image file: d3ma00413a-p6.tif

Dai-Viet N. Vo

Dr Dai-Viet N. Vo received his PhD degree in Chemical Engineering from The University of New South Wales (UNSW), Sydney, Australia in 2011. He was a postdoctoral fellow at UNSW and Texas A&M University, Doha, Qatar. He was a Senior Lecturer at University Malaysia Pahang, Malaysia from 2013-2019. Dr Vo is currently the Deputy Director of Institute of Applied Technology and Sustainable Development, Nguyen Tat Thanh University, Ho Chi Minh City, Vietnam. His research area is the production of green synthetic fuels via Fischer–Tropsch synthesis using biomass-derived syngas from reforming processes. Dr Vo is the Assistant Subject Editor for the International Journal of Hydrogen Energy and Associate Editor of Environmental Chemistry Letters.

image file: d3ma00413a-p7.tif

Sowmya Appunni

Dr Sowmya Appunni received her PhD degree in Chemistry from the Gandhigram Rural Institute – Deemed University, India. She worked as a postdoctoral fellow and research associate at the SRM Institute of Science and Technology, Chennai, Tamil Nadu, India. Dr Sowmya is currently the Assistant Professor at the Chemical Engineering Department, KPR Institute of Engineering and Technology, Tamil Nadu, India. She is a dedicated researcher with teaching experience in chemistry and research expertise in various water treatment technologies, material chemistry especially polymers and composites; nanoparticles, photocatalysts, and sensors.

image file: d3ma00413a-p8.tif

Adaikala Selvan Gajendhran

Adaikala Selvan Gajendhran completed his master's degree in biotechnology from Bharathidasan Institute of Technology Campus, Anna University, Tiruchirappalli, Tamil Nadu. Now, he is working as an Assistant Professor in the Department of Biotechnology, Vinayaka Mission's Kirupananda Variyar Engineering College, Salem, Tamil Nadu, India. His research interests include applied microbiology, drug delivery and biofuels.


1. Introduction

Metal–organic frameworks (MOFs) are an emerging group of porous materials thoroughly explored in the past few years. MOFs are fabricated via effective self-assembly of metal ions with organic ligands via strong coordination bonds.1,2 The major characteristic features of MOFs are their porosity, tailored topologies, lower density, better void volume, and good chemical stability.3,4 In the MOFs, the well-arranged polycrystalline networks offer reactive sites in the form of metal centers and the ligand's functional group.5 Potential applications of MOFs include wastewater treatment,6 adsorption,7 air pollution treatment,7 photocatalysis,8 electrocatalysis,9 sensors,10 membranes,11 fuel cells,12 supercapacitors,13 batteries,14 food packaging,15 drug delivery,16 and tissue engineering.17 MOF-based materials always exhibited greater efficiency with tuneable properties.18 MOFs are easily processed in various forms like aerogels, hydrogels, thin films, membranes, composites, and fibers.2,19

Green or bio-based MOFs are yet another novel porous material. Bio-based MOFs are developed from renewable material sources that are environmentally benign, safe and non-toxic.20,21 Commonly employed bio-based materials are polysaccharides, amino acids, and peptides.22 The main advantage of using bio-ligands is the availability of multiple coordination sites and functional groups for binding ions.23 Other merits include abundance and availability, relatively lower cost, easy preparation routes, surface area, and chirality.24 In this study, chitosan (CS)/MOFs are focused on because of their biocompatibility and structural strength. Chitosan (CS) is chosen as a green source due to its availability, unique properties and versatile applications in medicine, energy and the environment.25–28 Although many research papers have been published on this subject, no comprehensive review paper is available on the preparation, properties and applications of chitosan/MOFs. However, Abdelhamid et al. (2022) reviewed preparations and applications of the cellulose based MOFs in the allied areas of environmental remediation, gas purifications, drug delivery and biomedical applications.2 The potential role of MOFs/cellulose composites in potential wastewater treatment was explored by Bej et al. (2023).29

This review paper highlights the significant developments attained by CS/MOFs for medical, environmental and energy applications (Fig. 1). The review briefs the preparation methods and properties of CS/MOFs. The study discusses diverse applications of CS/MOFs, such as the adsorptive removal of dyes, pharmaceuticals, heavy metals, photocatalysis, gas adsorption, membrane separation, supercapacitors, batteries, fuel cells, and packaging. Medical applications like antibacterial properties, drug delivery and tissue engineering are described. Finally, the advantages, disadvantages, and prospects are outlined.


image file: d3ma00413a-f1.tif
Fig. 1 An overall summary of the topics reviewed in this study. The important applications include wastewater treatment, air purification, sensing, food packaging, biotechnology and biomedical applications.

2. Chitosan

Chitosan (CS) is a natural fibrous polymer derivative of chitin N-deacetylation found to be a major constituent of crustaceans such as crabs, prawns, shellfish, shrimps and crawfish (see Fig. 2a).30,31 The fabrication of CS from chitin is elucidated in Fig. 2b. CS is an N-acetyl-2-amino-2-deoxy-D-glucopyranose unit possessing β-(1–4) bonds on the linear units.32 CS has been a wonderful polymer in the last few decades because of its abundance, renewability, biodegradability, biocompatibility, safety, affordability, and mucoadhesion-like properties, as shown in Fig. 2c.33–36 The chemical and physical characteristics highly depend on the molecular weight, degree of deacetylation, solubility, and degree of crystallinity of CS.34,35 The degree of deacetylation varies from 70 to 95% and influences the potential applications.37 The presence of the NH2 and OH usually determines the functionality of CS.38 NH2 can be easily protonated, enhancing the solubility in an acidic solution.39 Two hydroxyl groups are ascribed to modifying the CS's mechanical properties and solubility.
image file: d3ma00413a-f2.tif
Fig. 2 (a) Natural sources of CS such as crab shells, shellfish and prawns, (b) deacetylation of chitin into CS, and (c) important properties of CS such as environmental suitability, biodegradability, and hydrophilic nature etc.

CS also attracted commercial interest due to its greater nitrogen content than cellulose.40 The polymeric forms of CS are derived semi-synthetically from amino polysaccharides that possess unique properties, functionality and specific applications in the biomedical field.41 The flexibility offered by this bio-inspired material in creating bonds with the organic and inorganic compounds is because of its functional groups.42 Studies also claimed that CS and its derivatives display better applications because of their good solubility (water and other solvents). Conversely, chemically treated CS offers higher solubility in commonly used solvents. Furthermore, CS can be formulated into any desired shape or structure, such as powder, bead, membrane and scaffolds (see Fig. 3a). The important applications of CS (see Fig. 3b) include water remediation,43 catalysis,44 medicine,45 agriculture,46 textile,47 cosmetics,48 paper industry,47 food industry,28 drug delivery,33 and nanotechnology.49


image file: d3ma00413a-f3.tif
Fig. 3 (a) Different formulations of CS into hydrogels, nano-particles, membranes, scaffolds, and bio-printing, and (b) applications of CS-based materials in the field of environment, medicals and food packaging.

3. Metal–organic frameworks

Metal–organic frameworks (MOFs) or porous coordination polymers are a prominent group of highly crystalline microporous materials developed based on principles of coordination chemistry.1 MOFs are formulated based on the self-assembly of organic linkers and coordination nodes of the metal ions or the cluster of metal ions.50 Metal ions such as aluminium, copper, zinc, titanium, magnesium and zirconium are used to fabricate MOFs.51 The MOFs can be developed into morphologies like 1, 2 and 3 dimensional structures.52 The main structural characteristics of MOFs are their phenomenal porosity of 90% for their free volume and greater internal surface area (>10[thin space (1/6-em)]000 m2 g−1).1,53 These properties make MOFs perfect materials for adsorption,54 photocatalysis,55 supercapacitors,56 batteries,57 sensors,52 and biomedical applications.58 As per the Cambridge structure database, about 70[thin space (1/6-em)]000 structures of MOFs are available. Commonly reported MOFs (see Fig. 4) are zeolitic imidazolate frameworks (ZIF),59 Universiteteti Oslo (UiO-66),60 Hong Kong University of Science and Technology (HKUST-1),61 and Materials for Institute Lavoisier (MIL-53).62 The advantages of MOFs are their phenomenal surface area and porosity, size selectivity, good optical properties, mechanical and thermal stability, higher density of transition metals, and capability to control the compositions and structure of MOFs. The disadvantages include (i) their lower electrical conductivity, (ii) the poor recovery and reusability of the powdered MOFs are undesirable for several applications including water remediation, and (iii) their higher fabrication costs and lower stability always hinder the utilization in large-scale operations.
image file: d3ma00413a-f4.tif
Fig. 4 Structures of different MOFs. The Commonly employed MOFs are ZIF-8, MIL-53, HKUST-1 and MIL-53. Reproduced with permission.63 Copyright 2015, Royal Society of Chemistry.

4. Chitosan/MOFs

The formation of biopolymer/MOFs is a promising solution to surmount the hereditary restraints related to the stability and recyclability of the MOFs.23 Several researchers stressed the conjugation of different biopolymers like CS, cellulose, and cyclodextrin onto the MOFs. The hybrid materials prepared using CS and MOFs displayed the characteristics of both CS and MOF, along with the new properties formed via strong interaction between MOFs and CS as indicated in Fig. 5.25 In most cases, hybrid materials are stabilized by appropriate complexation between the MOF's metal center and CS's functionality. The diagrammatic representation of CS/MOF is shown in Fig. 5. The inclusion of CS with MOFs resulted in exceptional stability, better optical properties, conductivity, adsorption capacity, flexibility and mechanical properties. The important advantages of CS/MOFs are depicted in Fig. 5.
image file: d3ma00413a-f5.tif
Fig. 5 Diagrammatic representation of CS–MOFs and their important advantages make them suitable for diverse applications.

4.1 Design criteria for CS bio-polymeric ligand in MOFs

The preparation of MOFs involves metal ions and an organic ligand responsible for forming coordination bonds, yielding a crystalline structure with greater surface area and better efficiency.64 Several MOF types are reported for diverse sector applications.65 Recently, CS-based MOFs have emerged from combining MOF-based chemistry and science.66 Even though exact definitions for bio-MOF or CS/MOFs do not exist, two different aspects are highlighted in the literature: (a) inclusion of a biomolecule as a ligand in the development of MOFs, and (b) greater porosity after incorporating a natural material.23 Including bio-inspired materials may attribute new features and extend their applications to other fields. As a result, some strategies are proposed to yield highly efficient CS/MOFs.67

• Utilization of CS as one of the organic ligands during the preparation of MOFs.

• The formation of composites via covalent coupling with the MOF linkers through post-preparation strategies.

• CS is also used as a bio-ligand, and it may ensure the biocompatibility, crystallinity, and functionality of the prepared CS/MOFs.

4.2 Synthesis of CS/MOFs

The CS/MOFs can be developed through in situ and ex situ strategies (Fig. 6). The ex situ method involves the inclusion of prepared MOFs into the respective form of CS. The ex situ approaches include direct mixing, and immersion coating. In direct mixing, MOFs are directly mixed with a CS solution (Fig. 7a). In the immersion coating, the CS-based template or scaffolds is immersed into the solution containing MOF particles. The main advantages are the ability to control MOFs loading with CS, better surface area and greater adsorption capacity. Still, this method is highly time-consuming and requires several chemicals.2
image file: d3ma00413a-f6.tif
Fig. 6 Fabrication of CS/MOFs using different methods.

image file: d3ma00413a-f7.tif
Fig. 7 Schematic representation of different preparation strategies like (a) direct mixing, (b) step-wise in situ growth and (c) a layer-by-layer strategy for the preparation of CS/MOFs.

In the in situ approach, MOF precursors are directly added to the CS-based materials.2 The respective precursors are usually added to the unprocessed CS materials. Furthermore, the processed CS matrix undergoes freeze–drying to develop CS/MOF aerogels. Freeze drying is the simplest approach to yield porous composites. The yielded CS/MOF aerogel is a three-dimensional porous network cross-linked via van der Waals forces and hydrogen bonds.68 Different parameters like the CS to MOF ratio, concentration, and freezing rate define the stability and porous structure of aerogels. The crystallinity, porosity, and suitability of the CS/MOF aerogel make it suitable for diverse applications in water treatment.

The step in situ growth is the step-wise exposure of the MOF precursor with the CS solution (Fig. 7b). The addition of MOF precursors forms the effective coordination bond between the CS. Later, the inclusion of organic linkers initiates nucleation and growth.69 The layer-by-layer method is the in situ route in which the CS substrate is appropriately submerged in the metal-ion solution (Fig. 7c). It is subsequently submerged in the organic ligand solution and vice versa.70 Homogeneous morphology and controlled thickness are offered by this method. The in situ growth is related to the step-wise exposure of the CS substrate to the respective MOF precursor. Initially, inclusion of the metal precursor forms an initial coordination between the metal ions and the functional groups of the CS. Finally, the organic linkers are added for nucleation and growth. Advantages of in situ methods include (i) a simple preparation route, (ii) better mechanical properties, (iii) better interaction between polymer and MOFs, and (iv) the ability to control the morphology and homogeneous distribution of MOFs.71 However, the precise control of the MOF loading on the CS is relatively complicated in the in situ strategy.

4.3 Processing of CS/MOFs

The CS/MOFs are easily formulated into different forms like aerogels, foams, hydrogels, thin films, and membranes. Methods like casting, dip-coating, electrospinning, filtration, and 3D printing can be adopted for the same, as illustrated in Fig. 8. Some of the methods are explained below:
image file: d3ma00413a-f8.tif
Fig. 8 Different preparation strategies of CS/MOFs adopted for different applications.

(a) Filtration is one of the most-simple fabrication routes that have attained phenomenal research interests in the last decade. The CS/MOFs suspension's solvent permeates through the membrane filter with the help of a vacuum. Finally, the CS/MOFs symmetrical structure is attained after drying. The merits of this method include high flexibility, permeability and porosity.

(b) Casting is a widely used method to build up Bio-MOFs mixed membranes. The matrix solution (preferably CS/MOFs solution) is poured slowly into a glass plate, followed by degassing, solvent extraction and drying. The formed membrane can be peeled off from the glass plate. Generally, the prepared membranes show greater permeability which is useful in water remediation and separation of gases.69

(c) Immobilization: the MOFs nanoparticles are immobilized on the surface of CS networks via crosslinking, encapsulation, etc.72 This method is highly useful for preparing CS/MOFs beads. It is also beneficial to avoid the loss of nanoparticles and improve reusability.73

(d) 3D printing: 3D printing is a trending strategy for preparing CS/MOFs. Major steps include CS/MOFs ink preparation, object structure design, and development upon computer-driven digital controller via a layer-by-layer strategy.74 3D printing offers greater reproducibility, low cost, easy scale-up, and porous structures.75,76

(e) Electrospinning: one-dimensional materials like fibers using polymers and MOFs precursors can be prepared using electrospinning.77 This route includes the preparation of nanofibers.78 The voltage is applied to the liquid stream and collector, allowing movement via a nozzle. Lastly, fibers are deposited at the collector after drying.31,73

(f) Freeze–drying is used to yield a highly porous CS/MOF composite. The freezing of the CS/MOFs is conducted at a lower temperature than the freezing point of a liquid. The aerogel is yielded from the sublimation of frozen small molecular solvents by means of liquid nitrogen freeze–drying methods.79 Freeze drying yields a three-dimensional porous network structure cross-linked via physical interactions like hydrogen bonds, chain entanglements, and electronic associations. The yielded aerogel exhibits high crystallinity and porosity and makes it suitable for diverse applications.69

5. Applications of CS MOFs

In the upcoming topics, we thoroughly explore the diverse uses of CS/MOFs. The broad applications of CS/MOFs include adsorption, catalysis, sensors, and membranes. The biomedical applications are explained with respect to wound healing, antibacterial, tissue engineering and drug delivery.

5.1 Adsorptive removal of pollutants

Adsorption is the most used wastewater remediation tool for treating the effluents seen in wastewater.80–82 The adsorption is highly preferred due to its easiness in operation, selectivity, cost-efficiency, and flexibility.83 However, adsorption poses several problems connected to the appropriate disposal and regeneration of CS/MOFs.84 Several researchers reported eliminating dyes, heavy metals, pesticides, phenols, and pharmaceuticals using CS/MOFs.
5.1.1 Dyes. Dyes are well-known coloured complex structures that exhibit affinity towards the substrates they applied.85,86 Almost forty thousand different dyes are available worldwide with an annual production of 45[thin space (1/6-em)]000 tons. Nearly 15% of these various dyes are directly discharged into the water through synthesis and application.31 Dyes are commonly employed in industrial sectors like textiles.87 Additionally, these dyes cause adverse health effects such as breathing problems, allergies, eye and skin disorders, and tissue necrosis.31,88 The growth of aquatic organisms is also hindered due to dyes and residues such as amines and imines in the marine environment.31,89 As these dyes resist bio-degradation, eliminating these noxious compounds is necessary for societal and environmental concerns.90

Saeed et al. (2022) discussed the preparation of CS/MOF-25 using the solvothermal method displaying an effective surface area of 30 m2 g−1. The adsorption experiments indicted an uptake capacity of 2857–2326 mg g−1 for CS/MOF-25, which is 14 times greater than CS, respectively. The hydrogen bonding, π–π bonding, pore-filling, electrostatic interaction and chemisorption were mainly responsible for the dye removal. The ethylene diamine functionalized ZIF-8 was incorporated into CS/PVA to form a membrane adsorbent to remove green 19. The membrane adsorbent was highly efficient in removing the dye, with a sorption capacity of 144.61 mg g−1. The removal rate is ascribed to the electrostatic interaction of ZIF-8 with dye yielded through surface modification of ZIF-8.91

Zhang et al. (2022) described the synthesis of core–shell hybrid aerogel using both ionic cross-linking and a coordination bonding strategy.92 A three-dimensional network of cellulose nanocrystals/carboxymethyl cellulose and MOF, respectively, form the core and shell of the generated aerogel beads. The produced aerogel spheres have a methylene blue adsorption capacity of 1112.2 mg g−1. The dye adsorption is mainly due to multilayer adsorption and follows the Freundlich isotherm model. Even after five cycles, only 20% reduction in adsorption capacity was observed.

Zhang et al. (2022) prepared different MOF-based adsorbents such as ZIF-8@attapulgite-CS, Zr-MOF@attapulgite-CS, and Al-MOF-@attapulgite-CS respectively. Both CS and attapulgite were added as supports to aid adsorption and enhance removal efficiency. Among these materials, Zr-MOF@attapulgite-CS illustrated a sorption capacity of 442.86 mg g−1 within 30 minutes of equilibrium time (methylene blue). This material also displayed reusability for up to five consecutive cycles without reducing removal efficiency. The system followed pseudo-second-order kinetics. The π–π interaction among the methylene blue and the organic ligand of Zr-MOF@attapulgite-CS is responsible for the degradation mechanism.93

Highly efficient CS/PVA/Uio-66/nanodiamond was developed via electrospinning for the destruction of Congo red (1430 mg g−1). Rational design of adsorbent enhanced the efficacy of the nanofiber which is ascribed to electrostatic attraction and repulsion. The developed nanofiber composite is flexible, porous, and permeable. Higher reusability is the predominant advantage of electrospun nanofibers.94 Chen et al. (2023) emphasized the fabrication of polyethyleneimine/CS/Ce-UIO-66 hydrogels via an ex situ blend method. The experimental studies indicated a maximum adsorptive elimination of methyl orange (900 mg g−1). The electrostatic interaction of hydrogen bonding very much helped in the reclamation of methyl orange.95

5.1.2 Pharmaceuticals. There is a steady increase in the concentrations of pharmaceutical compounds found in the aquatic environments due to the huge consumption of pharmaceuticals and improper waste management.80,96,97 Researchers also proved the existence of pharmaceuticals in different water matrices, for example, ground and surface water.98,99 The elimination of pharmaceuticals is a prerequisite to safe water.100,101

The MIL-101 (Fe)/ZnO-CS composite beads were fabricated via ionotropic gelation. The morphological studies claimed octahedral geometry and uniform size distribution for MIL-101 (Fe). With the incorporation of CS, a uniform spherical structure with a rough surface is observed with a surface area of 8.38 m2 g−1. MIL-101(Fe)/ZnO-CS composite beads reported a sorption capacity of 31.12 mg g−1 toward tetracycline removal. The sorbent also exhibited a removal efficiency of 90% even after five consecutive cycles. The π–π interaction among the aromatic rings of tetracycline and adsorbent was the responsible mechanism for the degradation of tetracycline.102 Yadav et al. (2022) emphasized preparing highly recyclable Fe3O4-functionalized MIL-101(Fe) CS beads using an ionotropic gelation method to eliminate antibiotics from water. The presence of CS is ascribed to the abundant number of active sites, adsorption, and flexibility of the beads. Scanning electron microscopy exhibited the greater adherence of the Fe3O4 particles on the rough surface of MIL-101(Fe). The sorption studies claimed a capacity of 45.33 mg g−1 for tetracycline. The bead also displayed excellent reusability for up to five cycles. The major mechanism for removing antibiotics using beads is π–π interaction and hydrogen bonding with electrostatic interaction.96

In another study, the adsorptive removal of ketoprofen and ibuprofen using MIL-101(Cr)/CS beads was carried out. The prepared CS beads demonstrated a very incremented surface area of 800 m2 g−1 compared with their pristine form (48 m2 g−1). Adsorption studies proved the viability of adsorbents in eliminating pharmaceuticals. The CS–MOF beads exhibited reusability for up to 7 cycles by maintaining the adsorption stability. The π–π interaction of aromatic groups between the adsorbent and pollutants is ascribed to the adsorption.103 Jia et al. (2021) conveyed the immobilization of CS grafted carboxylic acid Zr-MOF onto porous starch using a facile CS adhesives strategy. The presence of porous starch offers a unique macro-porous structure skeleton to accommodate UiO-66-COOH particles. On the other hand, CS strengthens the electrostatic interaction and hydrogen bonding with the MOF and porous starch. The CS binding decreased the adsorbent's surface area to 52.4 m2 g−1. The modified CS displayed an adsorption capacity of 50.25 m2 g−1 and reusability up to four cycles towards sulphanilamide.104

Later, Zhao et al. (2020) described the fabrication of MOF-incorporated CS beads for the reclamation of tetracycline. MOFs such as ZIF-8, ZIF-67, HKUST-1 and Fe-BTC were incorporated to form a bead to avoid the problem of poor reusability and the high cost of catalyst separation. Fig. 9a illustrates the preparation of CS/MOF beads using the in situ growth method. The CS/metal oxide beads from the acid-dissolved/alkali-solidified self-sphering process were adopted as a substrate for immobilizing MOFs. The metal oxide acted as the base template for the growth of MOFs. Among these materials, CS/ZIF-8 composite beads demonstrated a higher adsorption capacity of 495 mg g−1 and retained 90% and above tetracycline removal efficiency even after a number of cycles (see Fig. 9b and c). Both of these studies targeted enhancing the reusability of the adsorbent.105


image file: d3ma00413a-f9.tif
Fig. 9 (a) Diagrammatic representation of the CS/MOFs composite fabrication using the in situ growth method. (b) UV-vis spectra of tetracycline solution treated with different adsorbents. (c) Adsorption capability of the different adsorbents. Reproduced with permission.105 Copyright 2020, Elsevier.
5.1.3 Heavy metals. The discharge of heavy metals from industries has tremendously increased during the past decades, alarming both man and animals.106 Unlike other pollutants, heavy metals are not eliminated by microorganisms. As a result, they remain unchanged in the environment by increasing toxicity in soil, water, and the food chain. The heavy metals also cause severe health problems, including liver damage, skin disorders, damage to the nervous system, etc.107 Eliminating heavy metals is a prerequisite to ensure manhood's safety.

Hu et al. (2022) described the CS-assisted MOF dispersion using covalent bonding interaction to eliminate heavy metals from wastewater. Here, a new strategy was proposed to overcome the problems associated with serious agglomeration. UiO-66-NH2 was chosen as the MOF material and grafted on CS via covalent interaction with the help of glutaraldehyde. The study reported that grafting MOFs onto the CS structure improved the MOF's dispersion and retained the MOF's morphology. However, incorporating CS reduced the surface area of UiO-66-NH2 from 781.5 to 363.9 m2 g−1 due to non-porous CS. The experiments reported a maximum sorption capacity of 364.96 and 555.56 mg g−1 for Cu(II) and Pb(II) within 45 minutes, respectively.108

Huang et al. (2022) emphasized the fabrication of MOF-derived Co–Al-LDH@CS/Fe3O4 for the elimination of Pb(II) and Cr(VI). The Pb(II) and Cr(II) sorption capacities are 558.84 and 710.79 mg g−1, respectively. The adsorption kinetics proved that sorption occurred via chemisorption, and the rate-limiting step is exterior dispersion. The prepared adsorbent displayed better selectivity and reusability up to five cycles. The density functional theory proved the –SH and –NH2 present on the surface of Co–Al-LDH@CS/Fe3O4 exhibited good affinity towards heavy metals. Chelation and electrostatic interaction was the responsible mechanism for heavy metal removal, which was proved via XPS analysis and zeta potential.109

Zhu et al. (2022) described the in situ growth of ZIF-8 on the carboxymethyl CS beads for the enhanced adsorption of Pb(II) ions present in wastewater. The sorption experiments reported a maximum adsorption capacity of 566.09 mg g−1 with reusability of 4 cycles. The studies proved the phenomenal role of NH2 and COOH in the carboxymethyl CS in the chelation of lead ions.110 Zaman et al. (2022) focused on the microwave-assisted preparation of CS-UiO-66-glycidyl methacrylate MOFs to remove Pb(II). The formulated sorbent indicated a phenomenal surface area of 867 m2 g−1 with a thermal stability of 400 °C. The CS–MOFs retained 83.45% removal efficiency after 5 cycles.111 Wang et al. (2023) stressed the development of magnetic MIL-125-NH2/CS towards the reclamation of Cr(VI). The MIL-125-NH2/CS demonstrated a maximum sorption capacity of 109.46 m2 g−1 which is attributed to the uniform suspension of MIL-125-NH2/CS in water, higher surface area and greater number of active sites.112

5.1.4 Other pollutants. Luo et al. (2019) studied the potential capability of Al-MOF/sodium alginate–CS beads to eliminate bisphenol A. The surface morphology confirmed that incorporating CS made the beads smoother and decreased surface-exposed nanoparticles. Both sodium alginate and the CS experienced strong encapsulation due to interactions between the alginate and the CS leading to the formation of denser beads. The hybrid beads exhibited a very high surface area of 687.5 m2 g−1 and a micropore volume of 0.19 cm3 g−1. BET studies proved that CS was major in generating new micropores in the beads. The Al-MOF/sodium alginate–CS beads displayed a sorption capacity of 136.9 mg g−1 removal of bisphenol-A at a pH of 8 and 18 hours, respectively. The hydrogen bonding, π–π interaction, and cation–π bonding were major adsorption mechanisms for bisphenol remediation.113

Motaghi et al. (2022) reported that magnetic CS/activated carbon@UiO-66 usage for the ultrasound-assisted simultaneous adsorption of different noxious pollutants like Co(II), malachite green, and imidacloprid from aqueous streams. The adsorption studies claimed 44.5, 62.1, and 25.2 mg g−1 of adsorption capacity for Co(II), malachite green, and imidacloprid in the ternary system. The adsorptive process followed the PSO model, and thermodynamic studies indicate it is an endothermic process. Magnetic CS/activated carbon@UiO-66 is an environmentally friendly, cost-effective adsorbent with greater efficiency and reusability.114 Le et al. (2023) utilized an in situ strategy for the successful development of Cu-MOF/CS beads. The developed Cu-MOF/CS beads reported a 120 m2 g−1 adsorptive removal of toluene at 25 °C.115

Huang et al. (2020) emphasized the removal of 2,4-dichlorophenoxyacetic acid using ionic liquid-modified CS/UiO-66. A BET study claimed that the ionic liquid-modified CS/UiO-66 exhibited a surface area of 204.33 m2 g−1. Experimental studies claimed that the adsorbent exhibited a sorption capacity of 265.25 mg g−1. The better 2,4-dichlorophenoxyacetic acid removal is due to the increment in oxygen-containing groups, which promote the formation of hydrogen bonds in the adsorption.116 Yang et al. (2021) developed nano ZIF-8@CS micro-spheres using inverse emulsion and in situ growth methods. The experimental studies reported a sorption capacity of 128.7 mg g−1 for removing p-hydroxybenzoic acid from the agro-industry. The ZIF-8@CS microspheres also exhibited a maximum of three consecutive cycles.117

Overall, CS/MOFs exhibit exceptional properties in removing different organic pollutants. The major advantages of CS/MOFs are the high porosity with multifunctional groups functioning as active adsorption and high stability attributed to forming highly stable complexes with centered metal ions in MOFs. Table 1 summarizes different CS/MOFs for the adsorptive reclamation of noxious pollutants. Despite its excellent adsorption capacity, CS/MOF beads suffer several problems like:

Table 1 CS/MOFs for the adsorptive reclamation of noxious compounds
Adsorbent Preparation route Form Metal core Pollutant Adsorption capacity (mg g−1) Reusability Mechanism Ref.
ZIF-8 @CS poly vinyl alcohol Nanofiber Zn/Co Malachite green 1000 Electrostatic interaction 118
CS/UiO-66 Impregnation Composite Zr Methyl orange 370 4 Electrostatic interaction 54
HKUST-1 modified cellulose/CS composite Aerogel Methylene blue 526.3 5 Electrostatic attraction and hydrogen bonding 61
MIL-53/CS Hydrogel Fe Congo red 590.8 3 Pore filling and ionic interaction 119
Citric acid cross-linked Zn-MOF/CS Immobilization Composite Zn Methyl orange 220 5 Electrostatic attraction and cation-π interaction 120
ZIF-8@CS sponge In situ method Sponge Zn/Co Congo red 987 5 Electrostatic attraction 121
MIL-101(Fe)@ CS Immobilization Sponge Fe Acid red 94 4518 3 Hydrogen bonding and coordinate interactions 122
CS/Fe3O4/MII-101(Cr) Composite Cr Methyl orange 117 123
CS/UiO-66 Ice-templating Monolith Zr Congo red 246 4 124
TIF-A!/CS Secondary growth model Beads Al Pb(II) 397.3 5 Chelation 125
ZIF-67 modified bacterial cellulose/CS composite In situ method and lyophilisation Aerogel Co Cu(II) 200.6 5 Electrostatic interaction 126
5
ZIF-67@ aminated CS beads Beads Co Cr(VI) 119.05 7 127
CS-industrial hemp residue superfine powder-Fe@ZIF-67 Aerogel Co As(V) 22 128
CS-ZIF-8 In situ method Beads Zn/Co Cu(II) 165 5 Ion exchange 129
Pb(II) 131 5
CS-grafted-poly(N-vinyl caprolactam)-ZIF-8 Electrospinning Nanofibers Zn/Co Cr(VI) 269.2 5 Physical adsorption and π–π interaction 130
As(V) 258.5 5
MIL-100(Fe)/Fe2O4/CS Grafting Composite Fe Sb(III) 4 Surface complex binding of hydroxyl 131
ZIF-8@ CS microspheres Inverse emulsion and in situ growth Beads Zn/Co p-Hydroxybenzoic acid 128 3 Electrostatic interaction, hydrogen bonding 117
Porous starch CS-UiO-66-COOH Facile CS-adhesive strategy Composite Zr Sulfanilamide 4 Monolayer chemisorption 104
CS/ZIF-8 composite monolithic beads Beads Zn/Co Uranium 629 4 Chelation 132
CS-UiO-66 Simple gelation and freeze casting Beads Zr As(III) 47.9 5 Inner sphere complex 133
CS-graphene oxide/ZIF-8 In situ growth Foam Zn/Co Uranium 361 5 Electrostatic interaction, intraparticle diffusion and coordination 134
MOF-808/CS Composite Zr Cr(VI) 320 6 Hydrogen bonding and electrostatic interaction 135
Cu-MOF/alginate/CS/cellulose nanofibril composite In situ growth Hydrogel Cu Pb2+ 531.38 5 Ion exchange 136
CS/Uio-66-NH2 Composites Zr Hg2+ 896.8 6 137


• CS demonstrated lower solubility in water, negatively affecting the fabrication of MOF composites. The alteration of CS to a water soluble form is very difficult.

• The CS/MOFs beads are also susceptible to biofouling, and organic fouling during the sorption of noxious pollutants.

• The selectivity of CS is yet another concern during the adsorption process. This issue can be resolved by utilizing molecular printed CS and MOFs.

• The stability and the reusability of the CS/MOFs must be explored in detail. Special focus must be given to synthesizing beads, aerogels, and nanofibers for their extended reusability. Along with that, adsorption experiments using real wastewater are highly desired to understand the feasibility of the adsorbent.

5.2. Removal of gases and particulate matters

The primary cause of global warming is the unchecked generation of carbon dioxide from various human activities.138 In the past 150 years, carbon dioxide has increased from 250 to 418 ppm.2 The higher concentration of carbon dioxide in the environment causes health risks to human beings and the environment.139 The adsorptive-based carbon dioxide removal attained research importance due to its reversibility and versatility. For instance, Singo et al. (2017) also reported the preparation of CS-impregnated sodalite zeolite–metal MOFs to capture carbon dioxide. The adsorption studies were conducted in a packed bed reactor using 15% and 85% carbon dioxide and nitrogen, respectively. The impregnated CS/MOF displayed a maximum adsorption capacity of 978 mg g−1 at 25 °C.140

Jiamjirangkul et al. (2020) utilized MOF-integrated CS/PVA nanofibrous membrane hybrids to capture carbon dioxide. This study adopted three different strategies for the preparation of Cu-BTC/CS fibers hybrids via (i) direct mixing of Cu-BTC MOF with the CS/polyvinyl alcohol solution before electrospinning which was determined to be direct method, (ii) the formation of Cu-BTC MOF in CS nanofibers through an in situ method, and (iii) deposition of Cu-BTC MOF on CS nanofibre termed as the deposition method as highlighted in Fig. 10(I). Fig. 10(II) shows a diagrammatic representation of the preparation of Cu-BTC/CS nanofibrous hybrids via deposition of Cu-BTC/CS nanofibrous membrane. The nanofibrous membrane was successfully prepared via layer-by-layer deposition of Cu2+ as a metal cluster and BTC as an organic precursor to form Cu-BTC MOF nanoparticles on the surface of the fiber. Studies also proved that the prepared material's surface area and pore size is altered by changing the order of precursor mixing. The prepared membrane exhibited 14 times higher carbon dioxide sorption capacity.141


image file: d3ma00413a-f10.tif
Fig. 10 (I) Schematic illustration of different preparation routes of Cu-BTC/CS nanofibrous hybrids, (II) diagrammatic representation of the fabrication route of Cu-BTC/CS nanofibrous hybrids via the deposition method. Reproduced with permission.141 Copyright 2020, Elsevier. (III) Reusability of the CS/PEO@MOF-5 membrane towards the removal of PM2.5, (IV) (a) SEM images of the CS/PEO@MOF-5 membrane treated with PM2.5, (b) higher magnification version of the SEM image, and (c) photos of the CS/PEO@MOF-5 membrane under different PM capture. Reproduced with permission.142 Copyright 2020, Elsevier. (V) Stability of MIL-125-NH2 incorporated bacteria cellulose/CS foams. Reproduced with permission.143 Copyright 2022, Elsevier.

In another study, CS/ZIF-8 beads were developed by the in situ growth method for carbon dioxide adsorption. The coordination of the free NH2 group present in the CS skeleton with Zn2+ and self-emulsifying properties played a phenomenal role in the in situ growth of ZIF-8 on the CS beads. The CS-ZIF-8 beads exhibited 90% adsorption of carbon dioxide in comparison with pristine ZIF-8. Carbon dioxide adsorption occurred via physical adsorption and exhibited more than 80% adsorption efficiency even after three consecutive cycles.144

Some researchers also tried other gases like formaldehyde. For example, Zhang et al. (2021) discussed the capability of CS cross-linked MOF-199@ aminated graphene oxide aerogel for the adsorptive removal of formaldehyde gas. The three-aerogel exhibited good thermal stability and reported a maximum sorption capacity of 197.89 mg g−1 of formaldehyde gas.145

Like carbon dioxide, air pollutants like particulate matter (PM)2.5 cause significant health issues.146 Air filtration is needed to overcome the exposure of particulate matter in our atmosphere.142 Pan et al. (2021) reported a MOF-5/electrospun CS/polyethylene oxide membrane to remove PM2.5. The CS/PEO@MOF-5 nanofiber membrane exhibited predominant PM2.5 filtration efficiency and a quality factor of 99.95% and 0.0737.147 A facile preparation strategy was proposed to efficiently integrate MOFs with cellulose paper and ZIF-8. The ZIF-8 was prepared via the in situ method in CS gel and followed by inclusion into the cellulose pulp to the composite design paper. The experimental studies reported 99.68% removal of PM2.5 with a base weight of 60 g m2. Fig. 10(III) emphasis the higher reusability of the CS/MOFs membrane with a PM2.5 removal efficiency of 96.46% at the 30th day with the increment in pressure drop. The morphological analysis of the CS/PEO/MOF-5 membrane after the passage of polluted air affirmed the homogeneous capture of particulates on the surface of the membrane (Fig. 10(IV)(a) and (b)). In Fig. 10(IV)(c), the CS/PEO@MOF-5 membrane possessed two sides, one side indicates polluted air and the B side indicates filtered air. The change in colour from white to yellow is seen with the increase in the filter time for cell A affirming the higher capture of particulate contaminants and the colour on the B-side indicates minor variations.142 Thus, the extraordinary structural integrity, durability and dust-holding capability of the modified membrane is claimed.

Hao et al. (2022) reported that MIL-125-NH2 incorporated bacteria cellulose/CS foams were used as an efficient air filter to remove particulate matter. The directional freeze–drying approach successfully synthesized the foam matrix composed of mesopores or macropores of the polymer skeleton, yielding accessibility towards the MOFs and reducing gas diffusion barriers. Studies reported a maximum filtration efficiency of 99.5% with long-term stability of 30 days (see Fig. 10(V)). The electrostatic interaction between the CS/MOFs and particulate matter was the predominant filtration mechanism.143

Overall, the CS/MOFs were able to remove toxic gases and particulate matter from the environment. The CS/MOFs exhibited good efficiency and stability. However, very limited studies were conducted using CS/MOFs. Continuing research is necessary to check the feasibility of CS MOFs against toxic gaseous pollutants. In addition, greater priority must be given to the beads, aerogels, hydrogels or membranes to ensure higher stability and reusability.

5.3 Catalytic applications

Photocatalysis is a highly utilized advanced oxidation process for wastewater treatment.82,84,148 Photocatalysis attained research importance due to its high efficiency, environmental friendliness, no formation of by-products and complete mineralization of pollutants.73 Very few researchers synthesized CS/MOF-based photocatalysts for environmental remediation. For example, an immobilized Cu3(btu)2-graphene oxide-CS hybrid photocatalyst was developed to remove methylene blue. The UV-diffuse reflectance spectra revealed a reduced band gap of 2.75 eV and an increment in the specific surface area to 947 m2 g−1. The photocatalytic degradation studies reported 98% methylene blue removal at a pH of 7 (time: 60 minute) using ultraviolet light.149

Vigneshwaran et al. (2022) emphasized the development of Fe2O3-supported micropillared Cu-BTC tethered over CS via the hydrothermal method. The MOF-based catalyst displayed 91% removal of paraquat within 60 minutes at a pH of 5. The hydroxyl radicals portrayed a major role in the reclamation of paraquat and followed pseudo-first-order kinetics. The CS/MOF displayed a maximum reusability up to 5 cycles. The improved reusability is ascribed to the magnetic behaviour of the photocatalyst (saturation magnetization of 9.565 emu g−1). The studies also claimed that the tuned band gap and hindered recombination increased visible light activity.150

The Zn2(BDC)2(DABCO)-CS-Fe3O4 nanocomposites were prepared by Ghourchian et al. (2021). SEM analysis reported the homogeneous dispersion of magnetic CS particles on the MOFs without any aggregation. The saturation magnetization of the prepared photocatalyst declined from 66 to 36 emu g−1. However, an increment in surface area is reported from 49.67 (MOF) to 148.83 m2 g−1 for the MOF-CS-Fe3O4. Experimental studies reported 99% removal of methyl orange within 23 minutes.151 Novel AgO-CoO-CdO/poly-alanine-CS reduced graphene oxide (rGO) nanocomposites were reported using the sonication approach with a band gap of 1.51 eV. The photo-studies indicated a 97.4% methyl orange redemption. The better catalytic potential is ascribed to the incorporation of poly-alanine-CS-graphene oxide nanocomposites, which easily trap visible light photons and minimize the recombination ratio of e-h+.152

Vigneshwaran et al. (2021) has researched the preparation of MIL-88(Fe)-TiO2-CS heterojunction via a solvothermal method. The composite removed 98.79% of monocrotophos within 30 minutes under visible light irradiation. The OH and O2˙ radicals played a prominent role in the reclamation of pesticides. The photocatalyst also exhibited stability for five cycles. The prepared heterojunction consists of several high-speed nano tunnels in the p–n heterojunction facilitating the movement of photo-induced charge carriers and limiting electron recombination.153

From the limited number of studies, it is clear that CS MOFs can be used as an effective photocatalyst. The CS/MOFs photocatalysts can be recovered and reused for multiple cycles without too many complications (Fig. 11a). The main advantages of CS/MOF photocatalysts are illustrated in Fig. 11b. Despite their phenomenal efficiency, the following points need to be addressed.


image file: d3ma00413a-f11.tif
Fig. 11 (a) Pictorial representation of recycling CS/MOFs as a photocatalyst for the reclamation of dye wastewater under visible light. (b) The advantages of CS/MOFs as an efficient photocatalyst are also highlighted.

• Extensive studies must be conducted on developing a low-cost synthesis route for CS/MOFs.

• Developing highly reusable photocatalytic beads via immobilization or using magnetic materials as support aids are highly required.

• No studies have been reported using solar light-driven CS/MOFs photocatalysis.

• Further studies are necessary to develop highly compact, cost and energy-efficient photocatalytic processes to enhance the catalytic activity to a greater extent.

A tandem reaction is an important reaction in which bonds are developed without isolating the intermediates, altering the reaction conditions or through inclusion of chemical reagents. Tandem reactions yield promising research attractions due to their simplicity and efficient utilization of atoms. Tandem reactions do not need any purification and separation of intermediate by-products. Zhao et al. (2020) explained the fabrication of CS-coated MIL-101(Cr) as effective catalysts for the tandem deacetalization-Knoevenagel condensation reaction. The CS-coated MIL-101(Cr) was fabricated via an in situ growth method, yielding good chemical and thermal stability and reusability. The CS coated MIL-101(Cr) exhibited a core (MIL-101(Cr))-shell structure (CS). Here MIL-101(Cr) possesses Lewis acidic sites, and CS provided both Brønsted acidic sites and Lewis basic sites. The synergistic effect between CS and MIL-101(Cr) offered a prominent catalytic activity toward the condensation reaction. The prepared catalyst also exhibited good reusability over five cycles.154

Yousefian et al. (2020) stressed the fabrication of Cu-MOF immobilized modified CS via combinations of terephthalic acid as an organic linker and Cu2+ as the metal constituent. The studies reported the Knoevenagel condensation reaction and the synthesis of benzylidene malononitrile under Cu-MOF/CS as an effective heterogeneous catalyst. The Knoevenagel products attained high yields under mild conditions and minimum time requirements. The catalyst is highly stable and exhibited high recovery for preparing benzylidene malononitrile derivatives. The catalyst is reused eight times without a reduction in the efficiency of the catalyst.155

Wang et al. (2022) stressed the growth of MOF on CS as an effective host for palladium as a catalyst for Suzuki reactions. The ZIF-8 has been planted on CS microspheres using polydopamine as the base substrate. The preparation of CS/PDA@ZIF-8@Pd by employing CS spheres as base templates to grow MOFs as core–shell microspheres with the phenomenal surface area is shown in Fig. 12a. The CS/PDA@ZIF-8@Pd exhibited Kapp of 0.0426 s−1 for the reduction of p-nitrophenol. Fig. 12b represents the proposed mechanisms of the Suzuki coupling reaction using CS/PDA@ZIF-825@Pd. The ZIF-8 shells attached to CS microspheres via dopamine can fix Pd ions grown in its pores and restricts the size of Pd nanoparticles which provide a large number of active sites than larger Pd nanoparticles for quick electron transfer from an electron donor substrate to an acceptor to catalyze the p-NP and C–C coupling reaction. The unique core–shell structure possessing a surface area of 353.1 m2 g−1 was responsible for the unusual catalytic activity. The prepared catalyst demonstrated a reusability of 6 cycles with a final yield of 94% for CS/PDA@ZIF-825@Pd which is highlighted in Fig. 12c. The minor decline in yield of the catalyst is ascribed to the agglomeration of the catalyst and the presence of inorganic ions on the material surface.156


image file: d3ma00413a-f12.tif
Fig. 12 (a) Preparation route of CS/PDA@ZIF-8@Pd microspheres by employing CS spheres as the base template to grow MOFs as core–shell microspheres with a phenomenal surface area, (b) proposed mechanism of the Suzuki coupling reaction using CS/PDA@ZIF-8@Pd as the catalyst, and (c) reusability of different catalysts for Suzuki reactions. Reproduced with permission.156 Copyright 2022, Elsevier.

5.4 Membrane separation

The mixed matrix membrane yielded from CS and MOFs are highly popular in separation technology. The better performance is ascribed to the special features offered by MOFs. The high porosity, crystallinity, and surface area are important properties affecting the membrane's performance. Due to their improved mechanical properties, the CS/MOFs membrane exhibits high selectivity and withstands aggressive chemical environments. As a result, researchers are working in this field to enhance its potential applications.

Ma et al. (2017) developed a facile method for preparing a positively charged nanofiltration membrane. The membrane is prepared by blending both MOFs into the CS matrix for enhanced removal of cations. The MOFs, such as NH2-MIL-101(Al) and NH2-MIL-101(Cr), were uniformly dispersed in the CS matrix. Studies proved that the morphology of MOFs influenced the permeability of the membrane. The nanofiltration membrane of MOFs exhibited rod-shaped morphology and attained two times more flux. The rejection ratio of the nanofiltration membrane is found to be 93%.157 Wang et al. (2022) described the fabrication of sulfonated polyether sulfone/N-phthaloyl CS/MIL-101(Fe) as a novel mixed matrix cation exchange membrane. The presence of MIL-101(Fe) improved the ion-selective separation by forming a hydrogen bond with the CS matrix of the membrane. The desalination rate of the membrane improved by 136%, while the energy consumption was reduced to 90%.158

Shi et al. (2021) prepared a UiO-66/tannic acid/CS/polyethersulfone hybrid membrane to remove dyes and Cr(VI). The prepared material was dense enough to perform filtration experiments like a membrane to eliminate cationic and anionic dye from water. About 99% filtration efficiency achieved within 200 minutes is ascribed to the dynamic filtration ability created via an improved driving force that occurred via concentration polarization. Studies also claimed that the MOF was core in dispersing the tannic acid-CS mixture to enhance pollutant removal.159

Lakra et al. (2021) described the development of a cellulose acetate-CS–MOF forward osmosis membrane to recover water and nutrients. The forward osmosis is prepared by coating a CS AlFu-MOF mix on a cellulose acetate membrane. The AlFu-MOF membrane separation improved hydrophilicity and resulted in greater water flux. Experimental studies reported 80% water recovery in forward osmosis and 85% salt rejection from dilute draw solution using reverse osmosis. The nutrients in the concentrated feed wastewater are recovered as struvite by precipitating the reject water of reverse osmosis.160

Pervaporation is a highly economical method for separating azeotrope mixtures, recovering heat-sensitive compounds, and eliminating low-concentrated noxious compounds from the aqueous streams. Xu et al. (2022) reported the capability of the CS/ZIF-8 mixed matrix membrane to effectively separate methanol/dimethyl carbonate. Experimental studies reported that the 15 wt% CS/ZIF-8 membrane exhibited outstanding selectivity of 11.2 and MeOH performance of 97.7 GPU at 50 °C. The excellent efficacy is ascribed to the greater affinity of MeOH towards CS.161

Zhu et al. (2022) described the effective separation of methanol/dimethyl carbonate using the UiO-66 MOF/CS membrane. The studies emphasized that UiO-66 fillers improved the CS membrane's permeance and selectivity. A total flux of 355 g m−2 h−1 and a separation factor of 337 were achieved, almost 25 times greater than the pure CS membrane.162 Vinu et al. (2018) synthesized the microporous Al-MOF (Al(OH)(MBA)) using the hydrothermal and solvothermal methods. The MOFs were incorporated with the CS to form a mixed matrix membrane. The prepared MOF membrane effectively separated the water/ethanol mixture through pervaporation.163

The MOF (ZIF-8 or HKUST-1)/ionic liquid/CS mixed matrix membrane was successfully prepared to separate carbon dioxide/nitrogen. The presence of MOFs improved the selectivity of ionic liquid CS hybrid continuous polymer matrix. The experimental studies reported the permeability of the CO2/N2 selectivity performance is yielded for 10 wt% ZIF-8, and 5 wt% HKUST-1/ionic liquid CS membrane was 5413 Barrer and 11.5 and 4752 and 19.3 respectively. This is indicated by the better adhesion properties.164

Zhu et al. (2021) emphasized the preparation of the UiO-66-NH2 CS composite membranes for oil–water separation. The prepared membrane demonstrated high hydrophilicity in the air and super-oleophobic performance underwater. During the separation of petroleum ether water emulsion, the filtration flux is reported to be 2000 L m−2 h−1, and the filtration efficiency is greater than 95%. Even after ten cycles flux of the membrane was very high, four times greater than the mixed cellulose membrane.165 Si et al. (2023) focused on the separation of oil/water using ZIF-8@cellulose nanofiber/chitosan aerogel developed using a freeze-drying strategy. The predominant advantages of aerogels are higher porosity, light-weight and low density. The aerogel could easily separate oil from mixtures with assistance of gravity and displayed a reusability of 20 cycles.166

The CS/MOFs membranes are diverse materials exhibiting different applications in the allied areas of environment, separation and energy. Table 2 summarizes the different CS/MOF-based membranes for environmental remediation. Some of the challenges exhibited by CS/MOFs are.

Table 2 Different applications of CS/MOF membranes in environmental remediation in an aqueous matrix
Analyte Membrane MOF Separation mechanism Observations Ref.
Ethanol CS MOF-801 Pervaporation Flux = 1937 g m−2 167
Isopropanol CS ZIF-8 Pervaporation Flux = 410 g m−2 h 168
Ethanol CS ZIF-7 Pervaporation Flux = 322 g m−2 h 169
Methanol CS MIL-53 Pervaporation Flux= 2329 g m−2 h−1 170
Nitric oxide CS Cu-BTTri Filtration 171
BSA protein Polyvinylidene fluoride/CS UiO-66-NH2 ZIF-8 Ultrafiltration Flux = 470 L m−2 h 172
Rejection = 98.1%
Cr(VI) Rejection= 95.6%
Pb(II) Polyvinyl alcohol/CS UiO-66-NH2 Filtration Flux = 452 L m−2 h−1 173
Removal = 94%
Cd(II) Flux = 463 L m−2 h−1
Removal = 89%
Cr(VI) Flux = 479 L m−2 h−1
Removal = 85.5%


• The pre-synthesis of MOFs particles are highly necessary to ensure the removal of residual foreign molecules. The MOFs under vacuum may destroy pores and affect the sieving effect upon doping into the membrane matrix. The stronger pressure may also decrease the porosity. Activating the pore structure of MOFs using lower surface tension solvents is beneficial.

• The requirement of high temperature and organic solvents is necessary for the research of CS/MOFs. The preparation of MOFs at a higher temperature may cause secondary pollution to nature by forming toxic by-products and consuming organic solvents. It is always desirable to develop greener pathways for developing CS/MOFs.

• The majority of researchers emphasized the separation of pollutants via size exclusion selectivity. However, it is not easy to employ size-exclusion during the separation of molecules with more similar sizes and polarizability.

• The biopolymer-supported MOFs are highly prone to fouling, impacting the permeate quality and reducing the flux. The surface engineering of CS/MOFs may overcome this issue.

5.5 Energy storage devices

Ever-increasing energy demands and the continuous shortage of fossil fuels have compelled us to explore renewable energy resources. The challenge with energy storage devices must be addressed to exploit renewable energy sources.174 The need for sustainable elevated performance electrochemical energy storage and conversion devices is an emergency. The renewability, mechanical stability, flexibility, and durability makes the CS/MOFs suitable in different electrochemical energy storage and conversion devices such as supper capacitors, batteries and fuel cells.

Super capacitors are electrochemical energy storage devices that received the most research interest owing to their high power density, fast charging, and good cycle life.175 Novel electrode and electrolyte materials need to be developed to enhance the stability and durability of supercapacitors. Ehsani et al. (2020) reported the preparation of ternary poly-ortho aminophenol (POAP)/CS/MOF-1 using the electropolymerization method as an effective electrode in a pseudo-capacitor. Here, [Zn2(bdc)2(dbco)]n is used as a MOF in this study and was prepared via simple chemical routes with a surface area of 124.18 m2 g−1 for the ternary composite. The specific capacitance of the POAP/CS/DMOF-1 electrode is 3150 mF cm−2 at an optimum current density of 1 mA cm−2. The predominant capacitive activity is indicated by the synergistic effect of the CS/DMOF-1. The Faradaic contribution of the DMOF-1 enhanced the electrochemical performance of the electrode. The device retained 93% of its initial capacitance over 1000 cycles at 10 mA cm−2. The key merits of this composite electrode are higher active surface area, stability and easiness during the preparation.176

The hierarchically porous carbon derived from MOF/CS composites was used for the high-performance supercapacitor. A facile method was adopted for synthesizing porous carbon by calcinating MOF/CS composites. Studies claimed the prepared composite displayed a surface area of 2375 m2 g−1 and a pore volume of 2.49 cm3 g−1. The electrode exhibited a better specific capacitance of 199 F g−1 in 1 M H2SO4 electrolyte and a good rate capability of 75% from 0.05 to 4 A g−1. The supreme activity of the electrode is ascribed to the high surface area, pore volume, and the porous structure.177 Recently a team of researchers demonstrated the effective mechano-chemical route for the fabrication of ZIF-8 nanocrystals and ZIF-8@CS for battery applications. A novel lithium-ion battery anode material was developed by pyrolyzing the ZIF-8@CS nanocomposites. The material exhibits a high specific capacitance, lower impedance, and greater stability.178

A ZIF-8-derived porous carbon supported on carbon aerogel derived from CS was recently developed using the facile in situ deposition method followed by carbonization. Fig. 13(i) confirmed the deposition of ZIF-8 polyhedron on the CS aerogel through the co-precipitation followed by calcination. Fig. 13(ii) compares the carbon aerogel with the CS aerogel obtained at the end of the carbonation process resulting from the pyrolysis of CS. The prepared aerogel is also found to be lightweight and capable of standing on a flower petal. The stacked layer-by-layer three-dimensional porous structure is exhibited by carbon aerogels with interlaced nanosheets (Fig. 13(ii)(c)). The structural analysis also proved that the carbon aerogels boost-up the electron and ion transport and can be utilized as a base skeleton for the growth of ZIF-8 possessing a polyhedral structure. The prepared ZIF-8 exhibited an average particle size of 0.5 μm (Fig. 13(iii)(a)) and the corresponding SEM image in Fig. 13(iii)(b). Fig. 13(iii)(c) and (d) depict the SEM and TEM images of ZIF-8-C, which affirms the polyhedral shape after converting ZIF-8 to ZIF-8-C, respectively. The ZIF-8-C is uniformly supported and well-distributed on the nanosheets of carbon aerogels to restrict the aggregation of ZIF-8-C as observed in Fig. 13(iii)(e). The TEM image of the ZIF-8-derived porous carbon reinforced on carbon aerogel derived from CS affirms the uniform deposition of ultrafine nanocrystalline powder on the carbon sheets (Fig. 13(iii)(g)). The results also indicated the development of homogenously supported ZIF-8-C on the three-dimensional carbon aerogel nanosheets. Fig. 13(iii)(f) and (h) show the occurrence of nitrogen and carbon. The presence of nitrogen functional groups incremented the pseudo-capacitance in the charging–discharging process. The prepared material exhibited a three-dimensional mesoporous structure with interlaced nanosheets acting as a skeleton to grow ZIF-8-derived carbon. The presence of both mesopores and micropores creates more channels for electrolyte ions and provides electrical double-layer capacitance. Electrochemical performances revealed that the composite electrode exhibited a specific capacitance of 241.6 F g−1 at a current density of 0.5 A g−1 and retained a capacitance retention of 90% after 5000 cycles. The superior capacitive behaviour of the composite is indicated by the greater porosity of the continuous 3D structure which accelerated the electron/ion transport.179


image file: d3ma00413a-f13.tif
Fig. 13 (i) Schematic illustration of the formation of ZIF-8-carbon supported on carbon aerogel derived from CS. (ii) (a) A photograph of CS aerogel and carbon aerogel, (b) light-weight carbon aerogel on a flower, and (c) SEM images of the carbon aerogel. (iii) SEM images of (a) ZIF-8 and (b) ZIF-8-C, TEM images of (c) ZIF-8 and (d) ZIF-8-C, (e) SEM images of ZIF-8-carbon supported on carbon aerogel, (f) elemental mapping of carbon, (g) TEM images of ZIF-8-carbon supported on carbon aerogel, and (h) elemental mapping of nitrogen. Reproduced with permission.179 Copyright 2020, Elsevier.

The CS/MOFs are not well explored as a material for supercapacitors and batteries. Even though the results are good, further enhancement of the performance of the supercapacitor is necessary. The following parameters may require immediate attention to strengthen the efficacy of CS/MOFs as a supercapacitor or battery material. The fundamental mechanism behind the energy storage must be explored for interfacial reactions at the electrode. In addition, adequate control of interfacial interactions is important to attain a high electrochemical efficiency. To develop a full CS/MOFs-based supercapacitor, CS-based electrodes should be assembled with CS/MOFs electrolytes in a single device, and the performance must be evaluated.

Fuel cells are energy conversion devices that are capable of generating electricity via an electrochemical reaction using a fuel and oxidant. Recently, Kumar et al. (2022) stressed the fabrication of sulfonated CS and copper-based MOF (HKUST-1) based membranes using the solution casting technique for direct methanol fuel cell applications. The surface morphology proved the incorporation of HKUST-1 as a pore-filling agent and the creation of finger-like hydrophilic channels into the sulfonated CS matrix. The intermolecular hydrogen bonding between the carboxylic group of HKUST-1 and SO3H groups of sulfonated CS improves the performance in terms of ion exchange capacity, thermal stability, and proton conductivity. The prepared membrane possessed greater proton conductivities of 5.38 × 10−3 and 6.19 × 10−3 S cm−1 at 25 and 80 °C respectively. However, because of its small ionic size, the sulfonated CS membrane exhibited lower methanol permeability and selectivity than the pristine sulfonated CS and commercial membrane. The phenomenal pore reduction ability of HKUST-1 allowed proton and blocked methanol permeation in the membrane matrix.180

In another study, a highly efficient proton exchange membrane SO3H-UiO-66 coated halloysite nanotube-modified CS was formulated using a one-pot in situ growth method. Later it was used as an additive in the CS matrix to prepare the proton exchange membrane. The prepared membrane displayed strong mechanical strength and methanol resistance. The core–shell nanohybrids consist of 1-D halloysites nanotubes and MOFs with rich functional groups that enhance the water absorption characteristics. The core–shell nanohybrids eventually led to the development of interconnected water networks for speed proton transfer. As a result, the composite membrane displayed a conductivity of 46.2 mS cm−1 and a maximum power density of 84.5 mW cm−2.181 Further research is necessary to understand the capability of the CS/MOF.

5.6 Sensor applications

CS-based MOFs are a highly interesting material for sensing applications due to their gel-forming ability, hydrophilicity, better permeability, mechanical strength, and ease of employing reactive functional groups.

Choi et al. (2020) developed a co-hemin MOF/CS biosensor to detect lactose. The biosensor Co-hemin MOF was fabricated using the self-assembly of CoCl2 with an organic linker. Here, Co-hemin MOF acted as a mediator for the development of biosensors. The Co-hemin MOF was later adsorbed on a glassy carbon electrode through the electrodeposition method. Experimental studies reported that the prepared MOFs displayed phenomenal electrochemical performance in detecting lactose with a greater high sensitivity of 102.3 μA mM−1 (time = 5 s) and a lower detection limit of 4 mM.182 The biosensor also reported lactose in milk (46 g L−1), goat's milk (42.76 g L−1), drinking yogurt (5.99 g L−1) and chocolate milk (12.44 g L−1), respectively.

Huang et al. (2020) emphasized the development of CS/thiol functionalized MOFs for the detection of lead and cadmium ions in food samples. Under the optimized conditions, the detection limits of lead and cadmium ions were 0.33 and 0.008 μg L−1. The results of method validation offer excellent selectivity, high sensitivity and simple operation. The authors also validated the presence of lead and cadmium ions in three different certified reference materials (CRM) such as rice, wheat and tea. For example, the detected value of lead and cadmium are 0.021 μg g−1, 7 ng g−1, 0.059 μg g−1 and 15 ng L−1 for wheat and 1.6 μg g−1 and 64 ng L−1 for tea, respectively. The certified and the reported values were found to be in agreement with each other. Because the highly rich and accessible –SH functional groups of the CS/MOFs may accelerate the detection of lead and cadmium ions.183

Miao et al. (2022) emphasized the preparation of CDs@ZIF-8/CS as a portable, disposable test strip. Fig. 14(I) describes the CDs@ZIF-8/CS dual-function thin-film sensor assembly. The sensing material was developed by encapsulating luminescent porous composites and incorporating CS into it. The CS was an appropriate support to reduce the constraints related to secondary pollution impacted by powder composites. Along with this, the desired shape was also achieved. The formation of the CDs@ZIF-8 was indicated by the effective coordinate interaction between the Zn2+ and N-containing groups on the CDs surface during the ZIF-8 growth. The highly uniform sodalite zeolitic structure of ZIF-8 possesses a hexagonal shape with a size of 200 nm (Fig. 14(II)(a)–(d)). The introduction of the ZIF-8 to the CDs@ZIF-8 did not alter the morphology of ZIF-8. The film exhibited better sensitivity and selectivity for detecting tetracycline using a concentration quenching mechanism with a maximum detection limit of 0.60 μm (Fig. 14(III)).184


image file: d3ma00413a-f14.tif
Fig. 14 (I) Schematic preparation of the CDs@ZIF-8 CS dual function thin-film sensor (II) (a) TEM image of ZIF-8, (b) SEM image of ZIF-8, (c) TEM image of CDs@ZIF-8, and (d) SEM image of CDs@ZIF-8. (III) Performance for detection, selectivity, and adsorption of CDs@ZIF-8/CS film for tetracycline: (a) fluorescence quenching, and (b) selectivity of CS/MOF to tetracycline. Reproduced with permission.184 Copyright 2022, Elsevier. (IV) HPLC-MS/MS chromatograph of the different samples. Reproduced with permission.185 Copyright 2021, Elsevier.

The preparation of the MIL-101(Cr)/CS functionalized hydrophilic sponge column with the help of a simple infiltration method was reported. The CS minimized the problem of adsorption and hydrophobicity. The role of CS was to act as both adhesives during the functionalization of an adsorption adjuvant in detecting herbicides. The formulated material was used as an adsorbent in a vortex-assisted slid-phase extraction. It was combined with HPLC tandem MS to determine six triazines in water samples such as prometryn, desmetryn, atraton, ametryn, prometon, and dimethametryn as shown in Fig. 14(IV). The proposed method could determine these compounds in five real water samples. The triazine herbicide detection limit in spiked water samples ranges from 0.014 to 0.045 ng mL−1.185 The key highlights of this study include simplicity, higher sensitivity, and minimum requirements of organic pollutants.

Si et al. (2022) specifically focused on preparing MIL-53(Al)/CS/polyethylene oxide composite columnar foam to determine estrogen in an aqueous solution. Here, polyethylene oxide was used to serve as a porogen to enhance the MOF loading capacity of the prepared foam. The lower limit of estrogen detection is 0.3 to 6.6 ng L−1.186 Due to outstanding characteristics like surface area and porosity, they were suitable for detecting different pollutants and compounds. The synergistic effect of CS and MOF leads to enhanced efficiency in sensing heavy metals and pharmaceutical compounds.

5.7 Packaging

Food wastage is a predominant concern for a sustainable society.187 Active food packaging strategies can be adopted to reduce food waste, including incorporating active components into the packaging materials.28 Packaging can overcome the problems of traditional preservation methods like freeze–drying, microwave and fermentation as they cause a difference in the quality and taste of food.188 So, the CS/MOFs can be used as an active agent to increase shelf life and to ensure human health. The active agent, CS/MOFs packing, can be conducted via coating, sachets and an impregnation method, as shown in Fig. 15. However, a limited number of papers on CS/MOFs for food packaging are available.
image file: d3ma00413a-f15.tif
Fig. 15 CS/MOFs used in food packaging to preserve the food quality. Three methods for food packaging are adopted using MOFs: sachets, coatings, and impregnated packing.

The Ag@MOF-loded p-coumaric acid-modified CS/CS nanoparticle/PVA-starch bilayer film is used for food packing film. The novel bilayer film comprises two layers (i) Ag–MOF-p-coumaric acid-modified CS and (ii) PVA/starch as the top and bottom layers, respectively. The bilayer film displayed good oil resistance, antioxidant activity, cytotoxicity and optical properties. The film exhibited outstanding antibacterial activity against E. Coli and S. aureus. The surface of the bilayer film was highly smooth and exhibited a tensile stress of 27 MPa. The good UV-blocking properties, transparency, and ability to prevent bacterial infections make this film suitable for food industries.15

Kohsari et al. (2016) developed electrospun CS–polyethylene oxide nanocomposites composed of ZIF-8 using an electrospinning method. Studies reported that the CS-PEO-3%-ZIF-8 NPs could be highly adaptable for edible food coating due to its enhanced hydrophilic behaviour. The scanning electron microscopy affirmed the spherical ZIF-8 nanoparticles of 60 nm and the nanofibers with a diameter of 70 to 100 nm, respectively. Studies reported that the prepared nanoparticles were highly used for food packaging due to hydrophobicity and thermal and tensile properties.189

One pot-assisted silver-based MOF synthesis via CS cross-linking was proposed for fresh fruit keeping. The one-step preparation of Ag-MOFs@CS suspension with improved antibacterial properties. The interaction of silver ions with CS's NH2 and hydroxyl groups helps grow Ag-MOFs in the prepared matrix, which improves the effective dispersion and stabilization of Ag-MOFs and minimizes the release of Ag ions. The NH2 and OH of the CS interacted with the silver MOFs strengthening the aqueous stability and minimizing the silver toxicity. The weight of the untreated strawberries declined by 50%, and the sprayed CS/MOFs retained more than 70% of their initial weight. The problems related to food safety are also minimized via washability.190

The CS/MOFs possess potential applications due to their composition, structure and ability to form any shape. The major challenges to be addressed to meet large-scale food packaging applications are listed below:

• Further research is mandatory to predict the mechanical and functional features of CS/MOFs.

• Continuing research is mandatory to determine the level of hazard that CS/MOFs can cause, and studies on suitable materials can be selected for CS/MOFs packaging.

5.8 Medical applications of CS/MOF

CS/MOFs exhibited prominent applications in bio-medical fields due to their excellent antibacterial properties, environmental suitability and safety, biodegradability, biocompatibility and recyclability. The presence of the CS in CS/MOF minimizes the cytotoxicity of MOFs and hinders the penetration of metal ions into biological samples through isolation of metal ions.
5.8.1 Antibacterial applications. With the growing population, the effects of bacterial diseases are also rising, which causes extreme stress to human and animal health.191 In recent years, several nanomaterials have shown potential capabilities against eliminating the resistances and growth of bacteria.192 As per the reports, a few studies are also conducted for CS/MOFs for antibacterial applications. Fig. 16 indicates the antibacterial activity mechanism of CS/MOFs.
image file: d3ma00413a-f16.tif
Fig. 16 Mechanism of antibacterial properties of CS/MOF. The mechanism includes three pathways of metal ion release, accumulation in the cell wall, and linker release. This pathway causes enzyme disruption, cellular content mass leakage, and DNA and cell wall disruption.

Asl et al. (2022) developed Cu(II)-MOF@polydimethylsiloxane (PDMS) nanocomposite sponges coated with CS via blending of Cu-MOF into the PDMS sponge, followed by CS coating on the sponge via dip-coating. The developed sponges displayed good antibacterial efficiency against S. aureus and E. coli. The decline in the number of viable cells of bacteria is also reported. The biological studies also stressed that the prepared material provided adequate surface adhesion of cells, proliferation and viability.193 In the same year, MOF-derived ZnO/porous carbon-13X zeolite composite modified with CS and Ag nanoparticles was developed to study the antibacterial properties. Experimental studies reported that ZnO-MOFC/13X/CS/Ag displayed a high antibacterial activity depending on the inhibition zone diameter of 14.5 and 1.5 mm on both S. aureus and E. coli. The ZnO-MOFC/13X/CS/Ag demonstrated a higher surface area.194

Wang et al. (2020) incorporated Cu-MOF (HKUST-1) with electrospun CS/PVA fibers using the electrospinning method. HKUST-1/CS/PVA fibers displayed phenomenal antibacterial activity towards S. aureus and E. coli with an efficiency of 99%. The cytotoxicity test proved biocompatibility and cell adhesion.195 Zhang et al. (2021) described the ZIF/CS prepared by the in situ method to enhance the antibacterial effect. The synergistic interaction between the ZIF and CS strengthened the antibacterial effect more than its pristine form. The inhibitory rate for S. aureus and E. coli reaches 96 and 100% within 15 hours. The CS/ZIF composite could destroy the bacterial cell, and internal nucleic acid leakage and protein leads to an effective antibacterial effect. The HKUST-1/CS/PVA fibers exhibited higher stability for at least five days.196

The UiO-66-NH2 MOF nanoparticles with peroxidase and oxidase mimetic activities were blended with CS. The UiO-66-NH2/CS membrane exhibited peroxidase-mimicking behavior under peroxide, causing better antibacterial properties against Escherichia coli. The advantages of this membrane are its high stability, compatibility and hydrophilicity.197

Overall, CS/MOFs exhibited prominent antibacterial properties. However, most studies were conducted on S. aureus and E. coli, respectively. In addition to Gram-positive and Gram-negative organisms, experiments must be conducted on various organisms to understand the study's scope. Studies must be conducted in both in vivo and in vitro modes to assess the activity of the CS/MOFs. Utilizing polysaccharides and chemical agents can increase the activity of the CS/MOFs.

5.8.2 Drug delivery and therapeutic treatment. Drug delivery systems comprise one or more pharmacologically active compounds with a respective carrier. During the past decade, polymers have been extensively used in drug delivery, devices for drug encapsulation and controlled release. The CS/MOF is also adopted for drug delivery applications. CS exhibits several properties, such as safety, biodegradable, biocompatible, easy modification, etc., making CS/MOF unique. It is expected that CS/MOFs will work well for cancer therapy and other therapeutic applications (see Fig. 17).
image file: d3ma00413a-f17.tif
Fig. 17 Schematic representation of drug delivery using CS/MOFs and its potential applications in cancer therapy, skin repair, and brain disease treatment.

Dizaji et al. (2020) focused on the fabrication of PLGA/CS/MOF (ZIF-8 & MIL-101) nanofibers through electrospinning. The prepared PLGA/CS/MOF nanofibers were highly useful for the controlled release of paclitaxel against prostate cancer via in vivo and in vitro methods. The prostate loading capacity of the PLGA/CS/NaY, PLGA/CS/ZIF-8, PLGA/CS/ZSM-5, and PLGA/CS/MIL-101 are 81.2%, 91.2%, 83.9% and 87% respectively. The cell viability of the normal fibroblast cells treated with different samples was >85%, which highlights the lower cytotoxicity of the prepared carriers in normal cells and proves the biocompatibility of the nano-fibrous CS based MOF. A higher degree of drug release rate was observed in the acidic pH. The PLGA/CS/ZIF-8 loaded with paclitaxel reported 86% of cells are dead after three days.198

In another study, vancomycin, an antibiotic, was loaded into ZIF-8 nanocrystal for pH-controlled release. The ZIF-8/vancomycin was loaded into CS scaffolds to yield 3-D structures through wet spinning. The experimental studies reported that vancomycin loaded into ZIF-8 nanocrystals was released in pH control conditions from the CS scaffolds. Almost 70% of vancomycin was released in the 8th hour at a pH of 5.4. The scaffolds can act as a substitute for bone, and drug carriers may be used to treat infections like osteomyelitis.199 Lin et al. (2020) described the fabrication of carbon dot-embedded MOF@CS core–shell nanoparticles for drug delivery and vitro dual-mode imaging. Experimental studies were reported for doxorubicin as a model drug (50 mg g−1). It is noticed that the doxorubicin was released suddenly at a pH of 3.8, and the extent of release greatly differed at a pH of 7.4. Cytotoxicity proved the biocompatibility and suitability of drug transportation in humans and animals.200

Cao et al. (2021) described the CS-coated biocompatible ZIF-90 for the delivery of the methotrexate. The methotrexate was loaded into ZIF-90 via a Schiff base reaction between the NH2 in methotrexate and the aldehyde group of the imidazole-2-carboxaldehyde ligand with a loading of 250 mg g−1 (Fig. 18(a)). The outer layer modification of CS enhanced the pH responsiveness of the composite during drug release. The greater release of methotrexate under acidic conditions compared with under normal conditions under the normal environment. The cytotoxicity revealed that the prepared material CS@methotrexate@ZIF-90 minimized the growth of liver cancer HepG2 cells, prostate cancer DU145 cells and gastric cancer SGC7901 cells.201 A group of researchers studied the therapeutic efficacy of 5-fluorouracil and gemcitabine with minimum influence using MIL-101. The impregnation effect was used to encapsulate 5-fluorouracil alone and with the gemcitabine in the MIL-101. Studies claimed all nanocarriers displayed anti-cancer activities and induced apoptosis in the MCF-7 cells. The cytotoxicity in the HUVEC cells is because of the chemotherapy drugs.202


image file: d3ma00413a-f18.tif
Fig. 18 (a) Diagrammatic representation of CS-coated biocompatible ZIF-90 for the delivery of the anticancer drug methotrexate. Reproduced with permission.195 Copyright 2019, Elsevier. (b) Illustration of the synthesis of mesoporous carbon derived from CS-oligo nucleotides-two cell penetrating peptides and their gene delivery. Reproduced with permission.203 Copyright 2020, Elsevier.

Abdelhamid et al. (2020) discussed the carbonized CS encapsulated ZIF-8 for gene delivery. The mesoporous carbon materials were used as non-viral vectors to deliver genes using luciferase-expressing plasmid and splice-correction oligonucleotides. The illustration of surface modification of mesoporous carbon derived from CS-oligo nucleotides-two cell penetrating peptides and their gene delivery is indicated in Fig. 18(b). The carbon derived mesoporous carbon was effectively used as non-viral vectors for the delivery of two oligonucleotides named luciferase-expressing plasmid and splice correction oligonucleotides. These materials exhibited low toxicity and biocompatibility. The transfection using mesoporous carbon with and without cell penetrating peptides. The phenomenal transfection efficiency is due to the synergistic effect of mesoporous carbon and cell penetrating peptides.203

In another study, folic acid and doxorubicin incorporated UiO-66 loaded onto carboxymethyl CS/polyethylene oxide/polyurethane core–shell membrane for the controlled release. The drug loading efficiency of folic acid and doxorubicin is 95%. The maximum cell death percentage of the fibres under 0.3, 0.5, and 0.8 mL h−1 are 82, 83, and 8% after 168, 240, and 240 hours respectively. Studies also proved the enhancement of the apoptotic nuclei and the suitability of the fibers for cancer treatment.204

The MOF-808 based on zirconium tricarboxylate decorated folic-acid conjugated CS was efficiently used to deliver quercetin. The cytotoxicity was explored using MTT assay against the folate-receptor-negative HEK-293 and folate receptor-positive MCF7 cells. The MTT assay affirmed the internalizing efficiency of the nanoparticles, additional to the cytotoxic and apoptosis-induced properties. The mechanism of selective internalization of the MOF-808 loaded quercetin by CS-folic acid through the receptor-mediate endocytosis. The key merits of this material include low-cost, easiness in fabrication, high stability, higher drug release in acidic tumor environments, and active tumor-targeting through its higher affinity of folic acids on the tumor cell surface.205

Table 3 summarizes different applications of CS/MOFs in drug delivery. The studies show that CS/MOFs can be highly used for drug delivery and therapeutic applications due to their biocompatibility and biodegradability. However, lower solubility and high swelling properties are undesirable for incorporating hydrophobic drugs. The immunological and toxicological profiles of CS/MOFs must be studied for the endurance of complete safety.

Table 3 Drug delivery and therapeutic applications of CS/MOFs
Material Form Purpose Observation Application Ref.
Fe3O4@Bio-MOF-coated folic acid-CS conjugate Composite Tumor targeted delivery of curcumin and 5-fluorouracil Efficient drug loading capacity, controlled release of drugs, hemocompatibility and selective toxicity against cancerous cells Cancer therapy 206
Ni/Ta core–shell MOF coated with folic acid-activated CS nanoparticles Composite Targeted delivery of doxorubicin and curcumin Higher efficiency, high chemotherapeutic efficiency Cancer therapy 207
PAA-CS/PU/MIL-53 Fibers Co-delivery of paclitaxel and temozolomide against cancer cells Cancer therapy 208
PVA/Ag-MOF and PV/CS bilayer Hydrogel Tissue engineering of lung scaffolds Good antibacterial activity and poor biocompatibility Lung scaffold 209
Carbon dots embedded magnetic nanoparticle@CS@MOF Targeted doxorubicin delivery pH-Responsive drug release Cancer therapy 210
Cu(II) MOF@polydimethylsiloxane nanocomposite sponges coated with CS Sponge Tissue engineering Reduced number of viable bacteria cells Wound healing 193
MOF(HKUST-1) CS/PVA Membrane Wound healing The prepared material heals the wound and minimizes inflammation Skin repair 195
CS/bio-MOF Composite Targeted delivery of doxorubicin The maximum drug loading efficiency of 92% Cancer therapy 211
Chitosan/bacterial cellulose supported silver MOFs Composite Wound healing Tissue repair 212
CS/Al-MOF/GO Composite Drug delivery Biodegradability Cancer therapy 213


5.8.3 Tissue engineering. Bone tissue engineering and wound healing medicines are growing in regenerative medicine, which can be implemented by adopting different techniques such as nanotechnology, biomaterials, polymeric science and cell biology.

Khalili et al. (2020) focused on developing electroactive poly(p-phenylene sulfide)/r-graphene oxide CS scaffolds for wound dressing applications. Studies reported a decline in the hydrogel swelling ratio from 800 to 200% via poly(p-phenylene sulfide)/r-graphene oxide inclusion. The prepared material exhibited good biocompatibility and cell attachment as well. The porous structure was a prominent method for improving cellular activity and growth. The developed scaffolds displayed a porosity of 85%.214

Recently, Karakecili et al. (2022) focused on the preparation of UiO-66 acting as a double actor in CS scaffolds for the osteogenesis promoter. Studies reported that the wet-electrospun CS scaffolds possessing fosfomycin-loaded UiO-66 nanocrystals exhibited a fiber mesh structure with integrated micro-scale fibers and extremely high mechanical strength. The CS scaffolds were biocompatible with MC3T3-E1 pre-osteoblast, up-regulated the osteogenesis-related gene expression, and boosted the extracellular matrix mineralization.215

6. Future prospects

CS/MOFs offer outstanding physical and chemical properties, which are mandatory for various applications. CS is commonly employed as a modulator, support and binder for MOFs. The CS/MOFs are highly porous with multi-functional groups. Major advantages of CS/MOFs include (i) easy formulation into any shape, (ii) high porosity, flexibility, and better stability, and (iii) biodegradability. Despite the progress in the fabrication methods of CS/MOFs, some challenges must be addressed as follows:

(i) Complications in attaining ordered crystalline materials and predicting their topologies due to the poor symmetry of the bio-ligands.

(ii) Difficulty in maintaining porosity and open active sites in CS–MOFs.

(iii) Relatively harder to attain stability under relatively humid conditions.

• CS has a lower solubility in water, a major challenge in forming CS/MOFs materials. It is ascribed to the transformation of CS into a water-soluble form, which is highly beneficial during the fabrication of nanocomposites.

• All the MOFs do not exhibit the same mechanical strength. For example, HKUST displays a much lower mechanical strength. So, materials like graphene oxide and reduced graphene oxide can be blended into CS/HKUST to ensure the mechanical strength. However, low-cost materials can be used instead of graphene oxides for the endurance of mechanical stability.

• The structural stability of the CS/MOFs can be further increased via post-preparation modification which is beneficial for introducing several properties like the enhancement of porosity, number of catalytic sites, etc. Structural stability can be achieved via

(a) functionalization of the polysaccharides cross-linker.

(b) adopting covalent functionalization as a post-synthetic tool for modifying CS/MOFs. The combination of post-treatment methods can achieve the desired properties. Based on their properties, the post-synthetic modification for CS/MOFs must be selected.

• The CS/MOFs demonstrated several applications in energy, environment and medicine. In previous years, several studies were reported for preparing CS/MOFs. The basic relationship between the highly complex structures and the properties needs further research. Very minimal research is conducted in supercapacitors, fuel cells, batteries, packaging, and drug delivery. So, apart from the experimental studies and theoretical calculations, computational modelling is beneficial for understanding the relationship between various MOF units.

• CS/MOF composites are also prone to fouling which minimizes the pore size and surface roughness and block the functional groups of CS/MOFs. Fabricating fouling-resistant CS/MOFs is important to ensure the efficiency of the material.

• The cytotoxicity studies of the CS/MOFs must be performed in-depth in the allied areas of bio-medical and genetic engineering.

• CS possesses a unique specialty as it can be formulated into any desired shape, such as film, foams, beads and 3D scaffolds, with the help of 3D printing technology. For the preparation, researchers must use low-cost chemicals to ensure economic feasibility.

• CS/MOF composites are prominent adsorbents that remove dyes, pesticides, heavy metals and pharmaceuticals. However, utilizing CS/MOFs on a large scale still requires extensive studies. The preparation routes of most of these composites are time-consuming, and the processes are uneconomical. From an industrial perspective, simple and alternative preparation routes must be developed using low-cost and minimum consumption of toxic chemicals. Furthermore, these materials must exhibit higher reusability and ease of recoverability. The cost-effective regeneration tool is always an asset for commercialization.

• Continuing research is necessary on the current applications of CS/MOFs in the fields of energy storage devices, sensors, food packaging, and biomedical applications.

7. Conclusions

CS/MOFs are an evolving group of hybrid materials in materials science. Combining biopolymer CS within the MOF structure enhances the structural flexibility and robustness and eventually improves the physical–chemical characteristics of the hybrid materials. The CS/MOFs exhibit biological compatibility and flexibility due to the existence of CS in their structure. Studies also proved that the ligand is critical in altering functional MOFs' size, shape, and fabrication. The different preparation routes of the CS/MOFs and the post-modification methods are emphasized in detail. The potential applications of CS/MOF in the environment, energy and medical field are thoroughly highlighted. Among different applications, CS/MOF is highly reported as an adsorbent, in which ZIF-8@CS/polyvinyl alcohol exhibited 1000 mg g−1 of adsorption capacity against the removal of malachite green. As a hybrid material, CS/MOF is promising in different areas, such as supercapacitors, fuel cells, and food packaging. It is also evident that the CS/MOF found its importance in drug delivery and tissue culture. The major challenges of CS/MOF are difficult to attain a well-ordered crystalline structure with greater porosity and open active sites which accounts for the efficiency of CS/MOFs. Despite the clarity of mechanisms, it can be anticipated that CS/MOFs are a highly smart and versatile material in the allied areas of materials science and technology.

Conflicts of interest

The authors declare no conflict of interest.

References

  1. Q. L. Zhu and Q. Xu, Chem. Soc. Rev., 2014, 43, 5468 RSC.
  2. H. N. Abdelhamid and A. P. Mathew, Coord. Chem. Rev., 2022, 451, 214263 CrossRef CAS.
  3. C. Vaitsis, G. Sourkouni and C. Argirusis, Ultrason. Sonochem., 2019, 52, 106 CrossRef CAS PubMed.
  4. J. Ren, X. Dyosiba, N. M. Musyoka, H. W. Langmi, M. Mathe and S. Liao, Coord. Chem. Rev., 2017, 352, 187 CrossRef CAS.
  5. X. Wang, P. She and Q. Zhang, SmartMat, 2021, 2, 299 CrossRef CAS.
  6. D. Haldar, P. Duarah and M. K. Purkait, Chemosphere, 2020, 251, 126388 CrossRef CAS PubMed.
  7. C. Du, Z. Zhang, G. Yu, H. Wu, H. Chen, L. Zhou, Y. Zhang, Y. Su, S. Tan, L. Yang, J. Song and S. Wang, Chemosphere, 2021, 272, 129501 CrossRef CAS PubMed.
  8. Y. Shi, A. F. Yang, C. S. Cao and B. Zhao, Coord. Chem. Rev., 2019, 390, 50 CrossRef CAS.
  9. W. Zhou, J. Lu, K. Zhou, L. Yang, Y. Ke, Z. Tang and S. Chen, Nano Energy, 2016, 28, 143 CrossRef CAS.
  10. T. T. Tung, M. T. Tran, J. F. Feller, M. Castro, T. Van Ngo, K. Hassan, M. J. Nine and D. Losic, Carbon, 2020, 159, 333 CrossRef CAS.
  11. M. Kadhom and B. Deng, Appl. Mater. Today, 2018, 11, 219 CrossRef.
  12. X. Wen, Q. Zhang and J. Guan, Coord. Chem. Rev., 2020, 409, 213214 CrossRef CAS.
  13. B. Liu, H. Shioyama, H. Jiang, X. Zhang and Q. Xu, Carbon, 2010, 48, 456 CrossRef CAS.
  14. C. L. Song, G. H. Li, Y. Yang, X. J. Hong, S. Huang, Q. F. Zheng, L. P. Si, M. Zhang and Y. P. Cai, Chem. Eng. J., 2020, 381, 122701 CrossRef CAS.
  15. M. Zhang, Y. Zheng, Y. Jin, D. Wang, G. Wang, X. Zhang, Y. Li and S. Lee, Int. J. Biol. Macromol., 2022, 202, 80 CrossRef CAS PubMed.
  16. S. Mallakpour, E. Nikkhoo and C. M. Hussain, Coord. Chem. Rev., 2022, 451, 214262 CrossRef CAS.
  17. M. R. Ramezani, Z. Ansari-Asl, E. Hoveizi and A. R. Kiasat, Mater. Chem. Phys., 2019, 229, 242 CrossRef CAS.
  18. Z. Gao, M. Hou, Y. Shi, L. Li, Q. Sun, S. Yang, Z. Jiang, W. Yang, Z. Zhang and W. Hu, Chem. Sci., 2023, 14, 6860 RSC.
  19. J. Li, C. Wang, D. Wang, C. Yang, X. Cui, X. J. Gao and Z. Zhang, J. Mater. Chem. A, 2022, 20018–20023 RSC.
  20. H. Musarurwa and N. T. Tavengwa, Carbohydr. Polym., 2022, 275, 118743 CrossRef CAS PubMed.
  21. J. Zhu, X. Chen, A. Q. Thang, F. Li, D. Chen, H. Geng, X. Rui and Q. Yan, SmartMat, 2022, 3, 384 CrossRef CAS.
  22. H. S. Wang, Y. H. Wang and Y. Ding, Nanoscale Adv., 2020, 2, 3788 RSC.
  23. S. S. Nadar, L. Vaidya, S. Maurya and V. K. Rathod, Coord. Chem. Rev., 2019, 396, 1 CrossRef CAS.
  24. R. S. Forgan, Encycl. Inorg. Bioinorg. Chem., 2014, 1 CAS.
  25. H. Musarurwa and N. T. Tavengwa, Carbohydr. Polym., 2022, 283, 119153 CrossRef CAS PubMed.
  26. A. Leudjo Taka, M. J. Klink, X. Yangkou Mbianda and E. B. Naidoo, Carbohydr. Polym., 2021, 255, 117398 CrossRef CAS PubMed.
  27. P. Mohammadzadeh Pakdel and S. J. Peighambardoust, Carbohydr. Polym., 2018, 201, 264 CrossRef CAS PubMed.
  28. R. Priyadarshi and J. W. Rhim, Innov. Food Sci. Emerging Technol., 2020, 62, 102346 CrossRef CAS.
  29. S. Bej, H. Sarma, M. Ghosh and P. Banerjee, Environ. Pollut., 2023, 323, 121278 CrossRef CAS PubMed.
  30. A. Balakrishnan, S. Appunni and K. Gopalram, Int. J. Biol. Macromol., 2020, 161, 282 CrossRef CAS PubMed.
  31. P. Sirajudheen, N. C. Poovathumkuzhi, S. Vigneshwaran, B. M. Chelaveettil and S. Meenakshi, Carbohydr. Polym., 2021, 273, 118604 CrossRef CAS PubMed.
  32. S. K. Shukla, A. K. Mishra, O. A. Arotiba and B. B. Mamba, Int. J. Biol. Macromol., 2013, 59, 46 CrossRef CAS PubMed.
  33. A. Ali and S. Ahmed, Int. J. Biol. Macromol., 2018, 109, 273 CrossRef CAS PubMed.
  34. S. A. Qamar, M. Ashiq, M. Jahangeer, A. Riasat and M. Bilal, Case Stud. Chem. Environ. Eng., 2020, 2, 100021 CrossRef.
  35. M. Vakili, S. Deng, G. Cagnetta, W. Wang, P. Meng, D. Liu and G. Yu, Sep. Purif. Technol., 2019, 224, 373 CrossRef CAS.
  36. M. N. Ravi Kumar, React. Funct. Polym., 2000, 46, 1 CrossRef.
  37. V. Vendramin, G. Spinato and S. Vincenzi, Appl. Sci., 2021, 11, 1 Search PubMed.
  38. F. Zouaoui, S. Bourouina-Bacha, M. Bourouina, N. Jaffrezic-Renault, N. Zine and A. Errachid, TrAC, Trends Anal. Chem., 2020, 130, 115982 CrossRef CAS.
  39. S. G. Roy and P. De, J. Appl. Polym. Sci., 2014, 131, 1 CrossRef.
  40. M. Dash, F. Chiellini, R. M. Ottenbrite and E. Chiellini, Prog. Polym. Sci., 2011, 36, 981 CrossRef CAS.
  41. P. S. Bakshi, D. Selvakumar, K. Kadirvelu and N. S. Kumar, Int. J. Biol. Macromol., 2020, 150, 1072 CrossRef CAS PubMed.
  42. P. Sirajudheen and S. Meenakshi, Mater. Today Proc., 2020, 27, 318 CrossRef CAS.
  43. S. Appunni, M. P. Rajesh and S. Prabhakar, Carbohydr. Polym., 2016, 147, 525 CrossRef CAS PubMed.
  44. M. Hasmath Farzana and S. Meenakshi, Int. J. Biol. Macromol., 2015, 72, 1265 CrossRef CAS PubMed.
  45. F. S. Rezaei, F. Sharifianjazi, A. Esmaeilkhanian and E. Salehi, Carbohydr. Polym., 2021, 273, 118631 CrossRef CAS PubMed.
  46. Q. Zheng, D. Qin, R. Wang, W. Yan, W. Zhao, S. Shen, S. Huang, D. Cheng, C. Zhao and Z. Zhang, Int. J. Biol. Macromol., 2022, 220, 193 CrossRef CAS PubMed.
  47. N. Morin-Crini, E. Lichtfouse, G. Torri and G. Crini, Environ. Chem. Lett., 2019, 17, 1667 CrossRef CAS.
  48. S. Sakulwech, N. Lourith, U. Ruktanonchai and M. Kanlayavattanakul, Asian J. Pharm. Sci., 2018, 13, 498 CrossRef PubMed.
  49. M. Escamilla-García, G. Calderón-Domínguez, J. J. Chanona-Pérez, R. R. Farrera-Rebollo, J. A. Andraca-Adame, I. Arzate-Vázquez, J. V. Mendez-Mendez and L. A. Moreno-Ruiz, Int. J. Biol. Macromol., 2013, 61, 196 CrossRef PubMed.
  50. W. Chen, L. Du and C. Wu, Met. Fram. Biomed. Appl., 2020, 141 CAS.
  51. N. Manousi, D. A. Giannakoudakis, E. Rosenberg and G. A. Zachariadis, Molecules, 2019, 24, 1 Search PubMed.
  52. J. Annamalai, P. Murugan, D. Ganapathy, D. Nallaswamy, R. Atchudan, S. Arya, A. Khosla, S. Barathi and A. K. Sundramoorthy, Chemosphere, 2022, 298, 134184 CrossRef CAS PubMed.
  53. A. Al-Othman, M. Tawalbeh, O. Temsah and M. Al-Murisi, Encycl. Smart Mater., 2022, 535 Search PubMed.
  54. R. Ediati, W. Aulia, B. A. Nikmatin, A. R. P. Hidayat, U. M. Fitriana, C. Muarifah, D. O. Sulistiono, F. Martak and D. Prasetyoko, Mater. Today Chem., 2021, 21, 100533 CrossRef CAS.
  55. Y. Pan, X. Hu, M. Bao, F. Li, Y. Li and J. Lu, Sep. Purif. Technol., 2021, 279, 119661 CrossRef CAS.
  56. P. A. Shinde, M. A. Abdelkareem, E. T. Sayed, K. Elsaid and A. G. Olabi, Encycl. Smart Mater., 2022, 414 Search PubMed.
  57. V. Shrivastav, S. Sundriyal, P. Goel, H. Kaur, S. K. Tuteja, K. Vikrant, K. H. Kim, U. K. Tiwari and A. Deep, Coord. Chem. Rev., 2019, 393, 48 CrossRef CAS.
  58. S. Keskin and S. Kizilel, Ind. Eng. Chem. Res., 2011, 50, 1799 CrossRef CAS.
  59. B. Chen, Z. Yang, Y. Zhu and Y. Xia, J. Mater. Chem. A, 2014, 2, 16811 RSC.
  60. J. Chen, J. Ouyang, W. Chen, Z. Zheng, Z. Yang, Z. Liu and L. Zhou, Chem. Eng. J., 2022, 431, 134045 CrossRef CAS.
  61. Q. Liu, H. Yu, F. Zeng, X. Li, J. Sun, C. Li, H. Lin and Z. Su, Carbohydr. Polym., 2021, 255, 117402 CrossRef CAS PubMed.
  62. S. Gautam, H. Agrawal, M. Thakur, A. Akbari, H. Sharda, R. Kaur and M. Amini, J. Environ. Chem. Eng., 2020, 8, 103726 CrossRef CAS.
  63. P. Silva, S. M. F. Vilela, J. P. C. Tomé and F. A. Almeida Paz, Chem. Soc. Rev., 2015, 44, 6774 RSC.
  64. T. R. Cook, Y. R. Zheng and P. J. Stang, Chem. Rev., 2013, 113, 734 CrossRef CAS PubMed.
  65. S. El Hankari, M. Bousmina and A. El Kadib, Prog. Mater. Sci., 2019, 106, 100579 CrossRef CAS.
  66. K. Kim, S. Lee, E. Jin, L. Palanikumar, J. H. Lee, J. C. Kim, J. S. Nam, B. Jana, T. H. Kwon, S. K. Kwak, W. Choe and J. H. Ryu, ACS Appl. Mater. Interfaces, 2019, 11, 27512 CrossRef CAS PubMed.
  67. H. Nabipour, M. Mozafari and Y. Hu, Met. Fram. Biomed. Appl., 2020, 321 Search PubMed.
  68. M. da Silva Pinto, C. A. Sierra-Avila and J. P. Hinestroza, Cellulose, 2012, 19, 1771 CrossRef CAS.
  69. K. Tu, Y. Ding and T. Keplinger, Carbohydr. Polym., 2022, 291, 119539 CrossRef CAS PubMed.
  70. O. Shekhah, Materials, 2010, 3, 1302 CrossRef CAS.
  71. X. F. Zhang, Z. Wang, M. Ding, Y. Feng and J. Yao, J. Mater. Chem. A, 2021, 9, 23353 RSC.
  72. A. Kumar, G. Sharma, M. Naushad, A. H. Al-Muhtaseb, A. García-Peñas, G. T. Mola, C. Si and F. J. Stadler, Chem. Eng. J., 2020, 382, 122937 CrossRef CAS.
  73. A. Balakrishnan, S. Appunni, M. Chinthala and D. V. N. Vo, Environ. Chem. Lett., 2022, 20, 3071 CrossRef CAS.
  74. A. Jandyal, I. Chaturvedi, I. Wazir, A. Raina and M. I. Ul Haq, Sustainable Oper. Comput., 2022, 3, 33 CrossRef.
  75. L. Bergamonti, C. Bergonzi, C. Graiff, P. P. Lottici, R. Bettini and L. Elviri, Water Res., 2019, 163, 114841 CrossRef CAS PubMed.
  76. L. R. Yadav, S. V. Chandran, K. Lavanya and N. Selvamurugan, Int. J. Biol. Macromol., 2021, 183, 1925 CrossRef CAS PubMed.
  77. R. Jose Varghese, E. H. M. Sakho, S. Parani, S. Thomas, O. S. Oluwafemi and J. Wu, Nanomater. Sol. Cell Appl., 2019, 75 Search PubMed.
  78. P. Davoodi, E. L. Gill, W. Wang and Y. Y. Shery Huang, Biomed. Appl. Electrospinning Electrospraying, 2021, 45 CAS.
  79. A. Sharma, M. Thakur, M. Bhattacharya, T. Mandal and S. Goswami, Biotechnol. Rep., 2019, 21, e00316 CrossRef PubMed.
  80. M. Patel, R. Kumar, K. Kishor, T. Mlsna, C. U. Pittman and D. Mohan, Chem. Rev., 2019, 119, 3510 CrossRef CAS PubMed.
  81. M. Ponnuchamy, A. Kapoor, P. Senthil Kumar, D.-V. N. Vo, A. Balakrishnan, M. Mariam Jacob and P. Sivaraman, Environ. Chem. Lett., 2021, 19, 2425 CrossRef CAS.
  82. A. Balakrishnan, M. Ponnuchamy, A. Kapoor and P. Sivaraman, Legacy and Emerging Contaminants in Water and Wastewater. Emerging Contaminants and Associated Treatment Technologies, Springer, 2022, pp. 231–261 Search PubMed.
  83. G. Crini and E. Lichtfouse, Environ. Chem. Lett., 2019, 17, 145 CrossRef CAS.
  84. A. Balakrishnan, M. Sillanpää, M. M. Jacob and D.-V. N. Vo, Environ. Res., 2022, 213, 113613 CrossRef CAS PubMed.
  85. A. Gürses, M. Açıkyıldız, K. Güneş and M. S. Gürses, Dyes and Pigments: Their Structure and Properties, in Dyes and Pigments, Springer, 2016, pp. 13–29 Search PubMed.
  86. A. Balakrishnan, M. Chinthala and R. K. Polagani, Carbohydr. Polym., 2023, 121420 Search PubMed.
  87. M. Farhan Hanafi and N. Sapawe, Mater. Today Proc., 2020, 31, A141 CrossRef CAS.
  88. M. Ramesh and A. Muthuraman, Nat. Artif. Flavor. Agents Food Dye, 2018, 1 Search PubMed.
  89. J. Sharma, S. Sharma and V. Soni, Reg. Stud. Mar. Sci., 2021, 45, 101802 Search PubMed.
  90. A. Tkaczyk, K. Mitrowska and A. Posyniak, Sci. Total Environ., 2020, 717, 137222 CrossRef CAS PubMed.
  91. M. Khajavian, S. Shahsavarifar, E. Salehi, V. Vatanpour, M. Masteri-Farahani, F. Ghaffari and S. A. Tabatabaei, Chem. Eng. Res. Des., 2021, 175, 131 CrossRef CAS.
  92. Z. Zhang, J. Hu, X. Tian, F. Guo, C. Wang, J. Zhang and M. Jiang, Appl. Surf. Sci., 2022, 599, 153974 CrossRef CAS.
  93. W. Zhang, P. Sun, X. Wang, X. Zhang, L. Ran, Q. Zhao, B. Zou, L. Zhou and Z. Ye, Mater. Today Commun., 2022, 31, 103601 CrossRef CAS.
  94. F. Ahmadijokani, H. Molavi, A. Bahi, S. Wuttke, M. Kamkar, O. J. Rojas, F. Ko and M. Arjmand, Chem. Eng. J., 2023, 457, 141176 CrossRef CAS.
  95. Z. Chen, Z. B. Zhang, J. Zeng, Z. J. Zhang, S. Ma, C. M. Tang and J. Q. Xu, Carbohydr. Polym., 2023, 299, 120079 CrossRef CAS PubMed.
  96. D. Kanakaraju, B. D. Glass and M. Oelgemöller, J. Environ. Manage., 2018, 219, 189 CrossRef CAS PubMed.
  97. J. Wang and S. Wang, J. Environ. Manage., 2016, 182, 620 CrossRef CAS PubMed.
  98. E. P. Ambrosio-Albuquerque, L. F. Cusioli, R. Bergamasco, A. A. Sinópolis Gigliolli, L. Lupepsa, B. R. Paupitz, P. A. Barbieri, L. A. Borin-Carvalho and A. L. de Brito Portela-Castro, Environ. Toxicol. Pharmacol., 2021, 83, 103588 CrossRef CAS PubMed.
  99. V. Burke, D. Richter, J. Greskowiak, A. Mehrtens, L. Schulz and G. Massmann, Water Environ. Res., 2016, 88, 652 CrossRef CAS PubMed.
  100. L. Huang, R. Shen and Q. Shuai, J. Environ. Manage., 2021, 277, 111389 CrossRef CAS PubMed.
  101. A. Balakrishnan, E. S. Kunnel, R. Sasidharan, M. Chinthala and A. Kumar, Chem. Eng. J., 2023, 146163 CrossRef CAS.
  102. R. Vardhan Patel and A. Yadav, J. Mol. Struct., 2022, 1252, 132128 CrossRef CAS.
  103. N. Zhuo, Y. Lan, W. Yang, Z. Yang, X. Li, X. Zhou, Y. Liu, J. Shen and X. Zhang, Sep. Purif. Technol., 2017, 177, 272 CrossRef CAS.
  104. X. Jia, B. Zhang, C. Chen, X. Fu and Q. Huang, Carbohydr. Polym., 2021, 253, 117305 CrossRef CAS PubMed.
  105. R. Zhao, T. Ma, S. Zhao, H. Rong, Y. Tian and G. Zhu, Chem. Eng. J., 2020, 382, 122893 CrossRef CAS.
  106. X. Chen, M. F. Hossain, C. Duan, J. Lu, Y. F. Tsang, M. S. Islam and Y. Zhou, Chemosphere, 2022, 307, 135545 CrossRef CAS PubMed.
  107. M. Zaynab, R. Al-Yahyai, A. Ameen, Y. Sharif, L. Ali, M. Fatima, K. A. Khan and S. Li, J. King Saud Univ. – Sci., 2022, 34, 101653 CrossRef.
  108. S. Zhong Hu, T. Huang, N. Zhang, Y. Zhou Lei and Y. Wang, Carbohydr. Polym., 2022, 277, 118809 CrossRef PubMed.
  109. Z. Huang, C. Xiong, L. Ying, W. Wang, S. Wang, J. Ding and J. Lu, Chem. Eng. J., 2022, 449, 137722 CrossRef CAS.
  110. X. Zhu, J. Tong, L. Zhu and D. Pan, Int. J. Biol. Macromol., 2022, 205, 473 CrossRef CAS PubMed.
  111. H. Gul Zaman, L. Baloo, S. R. Kutty, K. Aziz, M. Altaf, A. Ashraf and F. Aziz, Environ. Sci. Pollut. Res., 2023, 30, 6216 CrossRef CAS PubMed.
  112. S. Wang, Y. Liu, Y. Hu and W. Shen, Int. J. Biol. Macromol., 2023, 226, 1054 CrossRef CAS PubMed.
  113. Z. Luo, H. Chen, S. Wu, C. Yang and J. Cheng, Chemosphere, 2019, 237, 124493 CrossRef CAS PubMed.
  114. H. Motaghi, P. Arabkhani, M. Parvinnia and A. Asfaram, Sep. Purif. Technol., 2022, 284, 120258 CrossRef CAS.
  115. V. N. Le, T. N. Tu and J. Kim, Sep. Purif. Technol., 2023, 306, 122718 CrossRef CAS.
  116. X. Huang, S. Feng, G. Zhu, W. Zheng, C. Shao, N. Zhou and Q. Meng, Int. J. Biol. Macromol., 2020, 149, 882 CrossRef CAS PubMed.
  117. S. Yang, Y. Wang, H. Li, Y. Zhan, X. Ding, M. Wang, X. Wang and L. Xiao, J. Porous Mater., 2021, 28, 29 CrossRef CAS.
  118. N. M. Mahmoodi, M. Oveisi, A. Taghizadeh and M. Taghizadeh, Carbohydr. Polym., 2020, 227, 115364 CrossRef CAS PubMed.
  119. Y. Jin, Y. Li, Q. Du, B. Chen, K. Chen, Y. Zhang, M. Wang, Y. Sun, S. Zhao, Z. Jing, J. Wang, X. Pi and Y. Q. Wang, Microporous Mesoporous Mater., 2023, 348, 112404 CrossRef CAS.
  120. C. Niu, N. Zhang, C. Hu, C. Zhang, H. Zhang and Y. Xing, Carbohydr. Polym., 2021, 258, 117644 CrossRef CAS PubMed.
  121. L. Liu, Y. Ma, W. Yang, C. Chen, M. Li, D. Lin and Q. Pan, New J. Chem., 2020, 44, 15459 RSC.
  122. Y. Wang, K. Wang, J. Lin, L. Xiao and X. Wang, Int. J. Biol. Macromol., 2020, 165, 2684 CrossRef CAS PubMed.
  123. L. Liu, J. Ge, L. T. Yang, X. Jiang and L. G. Qiu, J. Porous Mater., 2016, 23, 1363 CrossRef CAS.
  124. L. Wen, X. Chen, C. Chen, R. Yang, M. Gong, Y. Zhang and Q. Fu, Arabian J. Chem., 2020, 13, 5669 CrossRef CAS.
  125. Y. Ma, D. You, Y. Fang, J. Luo, Q. Pan, Y. Liu, F. Wang and W. Yang, Sep. Purif. Technol., 2022, 294, 121223 CrossRef CAS.
  126. D. Li, X. Tian, Z. Wang, Z. Guan, X. Li, H. Qiao, H. Ke, L. Luo and Q. Wei, Chem. Eng. J., 2020, 383, 123127 CrossRef CAS.
  127. A. M. Omer, E. M. Abd El-Monaem, M. M. Abd El-Latif, G. M. El-Subruiti and A. S. Eltaweil, Carbohydr. Polym., 2021, 265, 118084 CrossRef CAS PubMed.
  128. T. Chang, H. Lv, M. Tan, S. Zheng, W. B. Gao, B. Wang, Q. Zhao and B. Zhao, J. Sol-Gel Sci. Technol., 2022, 103, 730 CrossRef CAS.
  129. C. Wang, Q. Sun, L. Zhang, T. Su and Y. Yang, J. Environ. Chem. Eng., 2022, 10, 107911 CrossRef CAS.
  130. E. Bahmani, S. Koushkbaghi, M. Darabi, A. ZabihiSahebi, A. Askari and M. Irani, Carbohydr. Polym., 2019, 224, 115148 CrossRef CAS PubMed.
  131. N. Xiong, P. Wan, G. Zhu, F. Xie, S. Xu, C. Zhu and A. S. Hursthouse, Sep. Purif. Technol., 2020, 236, 116266 CrossRef CAS.
  132. L. Liu, W. Yang, D. Gu, X. Zhao and Q. Pan, Front. Chem., 2019, 7, 1 CrossRef PubMed.
  133. Y. Wei, R. Zou, Y. Xia, Z. Wang, W. Yang, J. Luo and C. Liu, Mater. Today Chem., 2022, 26, 101091 CrossRef CAS.
  134. X. Guo, H. Yang, Q. Liu, J. Liu, R. Chen, H. Zhang, J. Yu, M. Zhang, R. Li and J. Wang, Chem. Eng. J., 2020, 382, 122850 CrossRef CAS.
  135. F. M. Valadi, S. Shahsavari, E. Akbarzadeh and M. R. Gholami, Carbohydr. Polym., 2022, 288, 119383 CrossRef CAS PubMed.
  136. H. Zhao, J. Sun, Y. Du, M. Zhang, Z. Yang, J. Su, X. Peng, X. Liu, G. Sun and Y. Cui, J. Solid State Chem., 2023, 322, 123928 CrossRef CAS.
  137. X. Yan and H. Ge, Int. J. Biol. Macromol., 2023, 232, 123329 CrossRef CAS PubMed.
  138. T. R. Anderson, E. Hawkins and P. D. Jones, Endeavour, 2016, 40, 178 CrossRef PubMed.
  139. C. D. Keeling, Proc. Natl. Acad. Sci. U. S. A., 1997, 94, 8273 CrossRef CAS PubMed.
  140. M. C. Singo, X. C. Molepo, O. O. Oluwasina and M. O. Daramola, Energy Procedia, 2017, 114, 2429 CrossRef CAS.
  141. P. Jiamjirangkul, T. Inprasit, V. Intasanta and A. Pangon, Chem. Eng. Sci., 2020, 221, 115650 CrossRef CAS.
  142. J. Nie, H. Xie, M. Zhang, J. Liang, S. Nie and W. Han, Carbohydr. Polym., 2020, 250, 116955 CrossRef CAS PubMed.
  143. D. Hao, B. Fu, J. Zhou and J. Liu, Sep. Purif. Technol., 2022, 294, 120927 CrossRef CAS.
  144. C. Li, N. He, X. Zhao, X. Zhang, W. Li, X. Zhao and Y. Qiao, Chem. Sel., 2022, 7, e202103927 CAS.
  145. W. Zhang, T. Huang, Y. Ren, Y. Wang, R. Yu, J. Wang and Q. Tu, Int. J. Biol. Macromol., 2021, 193, 2243 CrossRef CAS PubMed.
  146. D. K. Yoo, H. C. Woo and S. H. Jhung, Coord. Chem. Rev., 2020, 422, 2213477 CrossRef.
  147. W. Pan, J. P. Wang, X. B. Sun, X. X. Wang, J. Yong Jiang, Z. G. Zhang, P. Li, C. H. Qu, Y. Z. Long and G. F. Yu, J. Cleaner Prod., 2021, 291, 125270 CrossRef CAS.
  148. A. Balakrishnan, K. Gopalram and S. Appunni, Environ. Sci. Pollut. Res., 2021, 28, 33331 CrossRef CAS PubMed.
  149. M. S. Samuel, S. Suman, Venkateshkannan, E. Selvarajan, T. Mathimani and A. Pugazhendhi, J. Photochem. Photobiol. B Biol., 2020, 204, 111809 CrossRef CAS PubMed.
  150. S. Vigneshwaran, P. Sirajudheen, V. P. Sajna, C. M. Park and S. Meenakshi, Environ. Sci. Pollut. Res., 2023, 30, 24876 CrossRef CAS PubMed.
  151. F. Ghourchian, N. Motakef-Kazemi, E. Ghasemi and H. Ziyadi, J. Environ. Chem. Eng., 2021, 9, 106388 CrossRef CAS.
  152. J. Zhang, E. Ding, S. Xu, Z. Li, A. Fakhri and V. K. Gupta, Int. J. Biol. Macromol., 2020, 164, 1584 CrossRef CAS PubMed.
  153. S. Vigneshwaran, P. Sirajudheen, P. Karthikeyan, M. Nikitha, K. Ramkumar and S. Meenakshi, J. Hazard. Mater., 2021, 406, 124728 CrossRef CAS PubMed.
  154. Z. S. Zhao, Y. Zhang, T. Fang, Z. B. Han and F. S. Liang, ACS Appl. Nano Mater., 2020, 3, 6316 CrossRef CAS.
  155. M. Yousefian and Z. Rafiee, Carbohydr. Polym., 2020, 228, 115393 CrossRef PubMed.
  156. G. Wang, J. Wang, Z. Chen and J. Hu, Int. J. Biol. Macromol., 2022, 206, 232 CrossRef CAS PubMed.
  157. X. H. Ma, Z. Yang, Z. K. Yao, Z. L. Xu and C. Y. Tang, J. Membr. Sci, 2017, 525, 269 CrossRef CAS.
  158. X. Wang, Q. Wang, M. Zhao, L. Zhang, X. Ji, H. Sun, Y. Sun, Z. Ma, J. Xue and X. Gao, Membranes, 2022, 12, 144 CrossRef CAS PubMed.
  159. P. Shi, X. Hu and M. DUan, J. Cleaner Prod., 2021, 290, 125794 CrossRef CAS.
  160. R. Lakra, M. Balakrishnan and S. Basu, J. Environ. Chem. Eng., 2021, 9, 105882 CrossRef CAS.
  161. X. Xu, Y. Hartanto, D. Nikolaeva, Z. He, S. Chergaoui and P. Luis, Sep. Purif. Technol., 2022, 293, 121085 CrossRef CAS.
  162. H. Zhu, R. Li, G. Liu, Y. Pan, J. Li, Z. Wang, Y. Guo, G. Liu and W. Jin, J. Membr. Sci., 2022, 652, 120473 CrossRef CAS.
  163. M. Vinu, D. Senthil Raja, Y. C. Jiang, T. Y. Liu, Y. Y. Xie, Y. F. Lin, C. C. Yang, C. H. Lin, S. M. Alshehri, T. Ahamad, R. R. Salunkhe, Y. Yamauchi, Y. H. Deng and K. C. W. Wu, J. Taiwan Inst. Chem. Eng., 2018, 83, 143 CrossRef CAS.
  164. C. Casado-Coterillo, A. Fernández-Barquín, B. Zornoza, C. Téllez, J. Coronas and Á. Irabien, RSC Adv., 2015, 5, 102350 RSC.
  165. X. Zhu, Z. Yu, H. Zeng, X. Feng, Y. Liu, K. Cao, X. Li and R. Long, J. Appl. Polym. Sci., 2021, 138, 50765 CrossRef CAS.
  166. R. Si, H. Luo, T. Zhang and J. Pu, Int. J. Biol. Macromol., 2023, 238, 124008 CrossRef CAS PubMed.
  167. Q. Li, Q. Liu, J. Zhao, Y. Hua, J. Sun, J. Duan and W. Jin, J. Membr. Sci., 2017, 544, 68 CrossRef CAS.
  168. S. Fazlifard, T. Mohammadi and O. Bakhtiari, Chem. Eng. Technol., 2017, 40, 648 CrossRef CAS.
  169. C. H. Kang, Y. F. Lin, Y. S. Huang, K. L. Tung, K. S. Chang, J. T. Chen, W. S. Hung, K. R. Lee and J. Y. Lai, J. Membr. Sci., 2013, 438, 105 CrossRef CAS.
  170. D. D. Kachhadiya and Z. V. P. Murthy, J. Environ. Chem. Eng., 2023, 11, 109307 CrossRef CAS.
  171. M. J. Neufeld, A. Lutzke, J. B. Tapia and M. M. Reynolds, ACS Appl. Mater. Interfaces, 2017, 9, 5139 CrossRef CAS PubMed.
  172. M. Pishnnamazi, S. Koushkbaghi, S. S. Hosseini, M. Darabi, A. Yousefi and M. Irani, J. Mol. Liq., 2020, 317, 113934 CrossRef.
  173. S. Jamshidifard, S. Koushkbaghi, S. Hosseini, S. Rezaei, A. Karamipour, A. Jafari Rad and M. Irani, J. Hazard. Mater., 2019, 368, 10 CrossRef CAS PubMed.
  174. M. Chinthala, A. Balakrishnan, P. Venkataraman, V. Manaswini Gowtham and R. K. Polagani, Environ. Chem. Lett., 2021, 19, 4415 CrossRef CAS.
  175. Poonam, K. Sharma, A. Arora and S. K. Tripathi, J. Energy Storage, 2019, 21, 801 CrossRef.
  176. A. Ehsani, M. Bigdeloo, F. Assefi, M. Kiamehr and R. Alizadeh, Inorg. Chem. Commun., 2020, 115, 107885 CrossRef CAS.
  177. S. Zhanng, M. Kitta and Q. Xu, Chem. – Asian J., 2019, 14, 3583 CrossRef PubMed.
  178. Y. Han, P. Qi, S. Li, X. Feng, J. Zhou, H. Li, S. Su, X. Li and B. Wang, Chem. Commun., 2014, 50, 8057 RSC.
  179. M. Wang, J. Zhang, X. Yi, X. Zhao, B. Liu and X. Liu, Appl. Surf. Sci., 2020, 507, 145166 CrossRef CAS.
  180. K. Divy, M. S. S. A. Saraswathi, A. Nagendran and D. Rana, J. Appl. Polym. Sci, 2022, 139, e52829 CrossRef.
  181. S. Zhao, Y. Yang, F. Zhong, W. Niu, Y. Liu, G. Zheng, H. Liu, J. Wang and Z. Xiao, Polymer, 2021, 226, 123800 CrossRef CAS.
  182. H. S. Choi, X. Yang, G. Liu, D. S. Kim, J. H. Yang, J. H. Lee, S. O. Han, J. Lee and S. W. Kim, J. Taiwan Inst. Chem. Eng., 2020, 113, 1 CrossRef CAS.
  183. L. Huang, W. Huang, R. Shen and Q. Shuai, Food Chem., 2020, 330, 127212 CrossRef CAS PubMed.
  184. M. Miao, L. Mu, S. Cao, Y. Yang and X. Feng, Carbohydr. Polym., 2022, 291, 119587 CrossRef CAS PubMed.
  185. Y. Jiang, Z. Qin, F. Liang, J. Li, Y. Sun, X. Wang, P. Ma and D. Song, J. Chromatogr. A, 2021, 1638, 461887 CrossRef CAS PubMed.
  186. H. Si, P. He, X. Wang, L. Li and X. Hou, New J. Chem., 2022, 46, 808 RSC.
  187. A. Sridhar, M. Ponnuchamy, A. Kapoor and S. Prabhakar, J. Hazard. Mater., 2022, 424, 127432 CrossRef CAS PubMed.
  188. A. Sultana, A. Kathuria and K. K. Gaikwad, Environ. Chem. Lett., 2022, 20, 1479 CrossRef CAS PubMed.
  189. I. Kohsari, Z. Shariatinia and S. M. Pourmortazavi, Int. J. Biol. Macromol., 2016, 91, 778 CrossRef CAS PubMed.
  190. Y. Zhang, Z. Lin, Q. He, Y. Deng, F. Wei, C. Xu, L. Fu and B. Lin, Appl. Surf. Sci., 2022, 571, 151351 CrossRef CAS.
  191. D. M. Morens and A. S. Fauci, PLoS Pathog., 2013, 9, e1003467 CrossRef CAS PubMed.
  192. G. Wyszogrodzka, B. Marszałek, B. Gil and P. Dorozyński, Drug Discov. Today, 2016, 21, 1009 CrossRef CAS PubMed.
  193. Z. Ansari-Asl, Z. Shahvali, R. Sacourbaravi, E. Hoveizi and E. Darabpour, Microporous Mesoporous Mater., 2022, 336, 111866 CrossRef CAS.
  194. E. Alrin, C. R. Tjampakasari and Y. K. Krisnandi, Inorg. Chem. Commun., 2022, 144, 109943 CrossRef CAS.
  195. S. Wang, F. Yan, P. Ren, Y. Li, Q. Wu, X. Fang, F. Chen and C. Wang, Int. J. Biol. Macromol., 2020, 158, 9 CrossRef CAS PubMed.
  196. M. Zhang, S. Ye, J. Wang, K. Yu, J. Cao, G. Li and X. Liao, Int. J. Biol. Macromol., 2021, 186, 639 CrossRef CAS PubMed.
  197. X. Wang, X. Zhou, K. Yang, Q. Li, R. Wan, G. Hu, J. Ye, Y. Zhang, J. He, H. Gu, Y. Yang and L. Zhu, Biomater. Sci., 2021, 9, 2647 RSC.
  198. B. Faraji Dizaji, M. Hasani Azerbaijan, N. Sheisi, P. Goleij, T. Mirmajidi, F. Chogan, M. Irani and F. Sharafian, Int. J. Biol. Macromol., 2020, 164, 1461 CrossRef CAS PubMed.
  199. A. Karakeçili, B. Topuz, S. Korpayev and M. Erdek, Mater. Sci. Eng., C, 2019, 105, 110098 CrossRef PubMed.
  200. C. Lin, K. Sun, C. Zhang, T. Tan, M. Xu, Y. Liu, C. Xu, Y. Wang, L. Li and A. Whittaker, Microporous Mesoporous Mater., 2020, 293, 109775 CrossRef CAS.
  201. X. X. Cao, S. L. Liu, J. S. Lu, Z. W. Zhang, G. Wang, Q. Chen and N. Lin, J. Solid State Chem., 2021, 300, 122259 CrossRef CAS.
  202. A. K. Resen, A. Atiroğlu, V. Atiroğlu, G. Guney Eskiler, I. H. Aziz, S. Kaleli and M. Özacar, Int. J. Biol. Macromol., 2022, 198, 175 CrossRef CAS PubMed.
  203. H. N. Abdelhamid, M. Dowaidar and Ü. Langel, Microporous Mesoporous Mater., 2020, 302, 110200 CrossRef CAS.
  204. A. Farboudi, K. Mahboobnia, F. Chogan, M. Karimi, A. Askari, S. Banihashem, S. Davaran and M. Irani, Int. J. Biol. Macromol., 2020, 150, 178 CrossRef CAS PubMed.
  205. M. Parsaei and K. Akhbari, Inorg. Chem., 2022, 61, 19354 CrossRef CAS PubMed.
  206. V. Nejadshafiee, H. Naeimi, B. Goliaei, B. Bigdeli, A. Sadighi, S. Dehghani, A. Lotfabadi, M. Hosseini, M. S. Nezamtaheri, M. Amanlou, M. Sharifzadeh and M. Khoobi, Mater. Sci. Eng., C, 2019, 99, 805 CrossRef CAS PubMed.
  207. S. Sadat Jalaladdiny, A. Badoei-dalfard, Z. Karami and G. Sargazi, J. Iran. Chem. Soc., 2022, 19, 4287 CrossRef.
  208. A. Bazzazzadeh, B. F. Dizaji, N. Kianinejad, A. Nouri and M. Irani, Int. J. Pharm., 2020, 587, 119674 CrossRef CAS PubMed.
  209. M. Zhang, G. Wang, X. Zhang, Y. Zheng, S. Lee, D. Wang and Y. Yang, Polymers, 2021, 13, 1 CAS.
  210. A. R. Chowdhuri, T. Singh, S. K. Ghosh and S. K. Sahu, ACS Appl. Mater. Interfaces, 2016, 8, 16573 CrossRef CAS PubMed.
  211. R. Abazari, A. R. Mahjoub, F. Ataei, A. Morsali, C. L. Carpenter-Warren, K. Mehdizadeh and A. M. Z. Slawin, Inorg. Chem., 2018, 57, 13364 CrossRef CAS PubMed.
  212. M. Barjasteh, S. M. Dehnavi, S. Ahmadi Seyedkhani, S. Y. Rahnamaee and M. Golizadeh, Surf. Interfaces, 2023, 36, 102631 CrossRef CAS.
  213. E. Aghazadeh Asl, M. Pooresmaeil and H. Namazi, Mater. Chem. Phys., 2023, 293, 126933 CrossRef CAS.
  214. R. Khalili, P. Zarrintaj, S. H. Jafari, H. Vahabi and M. R. Saeb, Int. J. Biol. Macromol., 2020, 154, 18 CrossRef CAS PubMed.
  215. A. Karakeçili, B. Topuz, F. Ş. Ersoy, T. Şahin, A. Günyakti and T. T. Demirtaş, Biomater. Adv., 2022, 136, 212757 CrossRef PubMed.

This journal is © The Royal Society of Chemistry 2023
Click here to see how this site uses Cookies. View our privacy policy here.