Cynthia J.
Castro
ab,
W. Camilla
Kuo-Dahab
a,
Tao
Jiang
a,
Sam
Downes
a,
Guoping
Zhang
a,
Ahmed S.
Abouhend
a and
Caitlyn S.
Butler
*a
aUniversity of Massachusetts Amherst, Department of Civil & Environmental Engineering, 18 Marston Hall, 130 Natural Resources Road, Amherst, MA 01003, USA. E-mail: csbutler@umass.edu
bWade Trim, 201 N Franklin St., Suite 1350, Tampa, FL 33602, USA
First published on 13th May 2024
Hydrostatic photogranulation represents an intriguing phenomenon with potential applications in aeration-free wastewater treatment. In this process, activated sludge batches transform into photogranules, manifesting as either spherical or disk-dominated shapes. Yet, the factors contributing to this morphological diversity remain unknown. Moreover, the impact of morphology on granule structure and physical characteristics remains poorly understood, posing potential implications for photogranulation in reactors that frequently utilize these hydrostatic granules as seeding materials. This study investigates the influence of water quality parameters on hydrostatic photogranulation and its role in shaping granule morphology. Spherical photogranules exhibited lower chlorophyll a concentration (5.97–7.40 mg L−1) and higher Chl a/b ratio (13−14) than disk-shaped photogranules (Chl a concentration: 8.13–11.70 mg L; a/b ratio: <10), indicating a higher cyanobacteria content in disk-shaped granules. Additionally, spherical photogranules showed significantly lower concentrations of EPS proteins and polysaccharides than disk-shaped granules, suggesting enhanced granulation under EPS limitations. Correlation analysis indicates that higher initial NO3− and total polysaccharides (TPS) increase the likelihood of producing spherical photogranules. Conversely, higher initial Ca2+ and Mg2+ concentrations were observed in cultivations predominantly producing disks. Furthermore, principal component analysis identified Cl−, Na+, NH4+, and SO42− as key initial water quality indicators and TPS, tCOD, and VSS as important sludge biomass characteristics that distinguished between different photogranule morphologies. Compared to spherical photogranules, disk-dominated photogranules exhibited higher stiffness and shear resistance, potentially due to increased cyanobacterial and EPS contents. Controlling hydrostatic photogranulation to achieve desired photogranule shapes holds potential for customizing seed granules and thus enhancing the OPG wastewater treatment performance.
Environmental significanceThis study unveils the opportunity to optimize the startup of the oxygenic photogranule (OPG) process by intentionally shaping seed hydrostatic photogranules. By discerning the impact of water quality on granule morphology, we present practical strategies to steer hydrostatic granulation towards enhanced reactor performance by attaining the desired photogranule shape. These insights pave the way for advancing the OPG process as an energy-efficient and sustainable wastewater treatment solution. By leveraging tailored approaches to granule formation, we can improve nutrient removal, enhance granule stability, and ultimately contribute to more effective and environmentally sound water treatment practices. |
According to the literature, OPGs can be generated under both hydrostatic conditions, which lack hydrodynamic shear, and under hydrodynamic conditions, where active mixing is employed.1–3,6,7,12 Despite being produced in distinct environments, hydrostatic and hydrodynamic photogranules exhibit striking similarities in morphology, internal structure, and microbial composition.1,2,13 Both types of granules are predominantly composed of filamentous and motile cyanobacteria belonging to the order Oscillatoriales, showcasing a layered structure where filamentous cyanobacteria form the outer layer encapsulating the inner non-cyanobacterial biomass.1,2,14 The primary distinguishing factor between these granule types is their size.1,2,6,14 The production of hydrostatic photogranules involves the transformation of activated sludge batches into photogranules under hydrostatic batch conditions with the presence of light.1–4,15 This transformation occurs through the enrichment of the phototrophic community within the sludge biomass, resulting in approximately 50% phototrophic content.1,4 The complete transformation takes approximately 2−4 weeks, yielding hydrostatic photogranules with a diameter up to 20 mm.1,4
Photogranulation under hydrodynamic conditions, i.e., in wastewater treatment systems, involves several methods,16–21 one of which is seeding hydrostatically formed granules in reactors with active mixing.2,5,7,13,14 When using hydrostatic photogranules as seeds, the hydrodynamic shear within the reactors causes these granules to disintegrate, releasing aggregates smaller than 100 μm in diameter that gradually develop into mature photogranules over time.1,2,7 Additionally, various types of seed biomass have been explored, including mixed cultures such as activated sludge with microalgal/cyanobacterial biofilm, aerobic granular sludge with unicellular green algae, or a combination of aerobic granular sludge and algae-bacterial granules.16–21
Seeding OPG reactors with hydrostatic granules or other types of reported phototrophic inoculums helps accelerate the process startup by promptly establishing a resilient microbial community, which facilitates a rapid transition to peak operational capabilities.2,7 However, utilizing different seed sources has resulted in the development of photogranules with diverse structures, microbial compositions, and sizes.1,3,13,16–20 When comparing various seeding methods, hydrostatic photogranules stand out for their well-defined characteristics and established production protocol, providing significant advantages in process reproducibility.1,2,4 Thus, using hydrostatic OPGs for reactor seeding ensures a consistent starting point compared to other seeds that lack well-defined characteristics and reproducibility protocols for the seed biomass.
It has been reported in multiple studies that hydrostatic cultivation of various sludge types, and sometimes even the same sludge biomass, undergoes contraction and compaction, leading to the formation of two distinct morphologies: disk and spherical granules.1,4,9,12 The disk morphology exhibits an ellipsoid shape with a filamentous outer layer, whereas the spherical granules appear with a smoother surface appearance.1,4,9,12 Additionally, given that these granules often serve as the primary seed biomass for hydrodynamic growth, their influence on photogranulation within reactors may be different, particularly during the critical startup phase. This variation could be attributed to differences in the distribution of shear forces across the particle surface. Despite its importance, the prevalence of one morphology over another in a given cultivation set remains unclear. Moreover, there is a lack of comprehensive information regarding the distinct physical attributes that differentiate spherical and disk-shaped granules.
This study aims to explore the factors influencing the morphological outcomes of photogranules produced under hydrostatic conditions. The objective is to gain a deeper understanding of the relationship between the initial wastewater characteristics in the local environment and the success of OPG cultivation, defined as the formation of a spherical or disk-shaped photogranule. Specifically, the study seeks to establish correlations between initial water quality parameters and the resulting OPG morphology, distinguishing between spherical and disk granules, across cultivation sets. Additionally, this study investigates the influence of physical parameters in the local cultivation environment on the formation of hydrostatic OPGs. In-depth investigations into the structural integrity and mechanical strength of hydrostatic photogranules with different morphologies are conducted to offer nuanced insights into the physical variations of OPGs and their potential implications for performance in wastewater treatment.
Am-100 | Ha-100 | Am-68.9 a | Ha-27.8 | Am-17.1 | Ha-14.3 | Am-13.8 a | ||
---|---|---|---|---|---|---|---|---|
a a = Cultivations used for material strength analysis. | ||||||||
Chl a | (mg L−1) | 0.416 | 0.315 | 2.04 | 0.341 | 0.510 | 1.10 | 1.24 |
Chl b | (mg L−1) | 0.852 | 0.163 | 2.60 | 0.105 | 0.310 | 0.410 | 1.95 |
Chl c | (mg L−1) | 1.18 | 0.171 | 3.17 | 0.055 | 0.184 | 0.171 | 2.35 |
VSS | (mg L−1) | 1783 | 2810 | 1973 | 2343 | 1113 | 2793 | 1620 |
Chl a | (mg g−1 VSS) | 0.233 | 0.112 | 1.03 | 0.146 | 0.458 | 0.394 | 0.765 |
tCOD | (mg L−1) | 2443 | 7109 | NA | 4301 | 1905 | 3561 | NA |
cBOD | (mg L−1) | NA | NA | 247 | NA | NA | NA | 143 |
TPS | (mg L−1) | 797.2 | 1366 | NA | 636.0 | 160.3 | 664.4 | NA |
TN | (mg L−1) | NA | NA | 23.8 | NA | NA | NA | 29.0 |
TKN | (mg L−1) | NA | NA | 24.4 | NA | NA | NA | 27.2 |
DIN | (mg N per L) | 15.3 | 12.6 | NA | 3.20 | 15.9 | 8.85 | NA |
Na+ | (mg Na per L) | 51.1 | 79.4 | NA | 104.2 | 71.0 | 109.0 | NA |
NH4+ | (mg N per L) | 6.53 | 2.33 | 19.5 | 1.26 | 15.9 | 7.95 | 18.9 |
K+ | (mg K per L) | 13.2 | 14.5 | NA | 17.4 | 12.6 | 16.9 | NA |
Ca2+ | (mg Ca per L) | 13.6 | 14.0 | NA | 38.1 | 48.9 | 53.0 | NA |
Mg2+ | (mg Mg per L) | 3.60 | 8.45 | NA | 29.4 | 9.94 | 15.0 | NA |
Cl− | (mg Cl per L) | 88.3 | 112.0 | NA | 150.0 | 93.2 | 137.0 | NA |
NO2− | (mg N per L) | 1.27 | 0.468 | NA | 0.113 | 0.00 | 0.754 | NA |
NO3− | (mg N per L) | 7.50 | 9.77 | NA | 1.83 | 0.067 | 0.145 | NA |
PO43- | (mg PO4 per L) | 1.10 | 2.09 | NA | 3.11 | 3.77 | 2.97 | NA |
SO42- | (mg SO4 per L) | 3.88 | 1.54 | NA | 13.6 | 7.80 | 12.7 | NA |
Cultivation name | Sludge source | Total vials | Total OPGs formed | Spherical OPGs | Disk OPGs | Spherical OPG formation (%) | Cultivation morphology |
---|---|---|---|---|---|---|---|
a a = Cultivation results were used only for material strength analysis. | |||||||
Am-100 | Amherst | 20 | 20 | 20 | 0 | 100 | Sphere |
Ha-100 | Hadley | 13 | 13 | 13 | 0 | 100 | Sphere |
Am-68.9 a | Amherst | 119 | 119 | 82 | 37 | 68.9 | Sphere |
Ha-27.8 | Hadley | 20 | 18 | 5 | 13 | 27.8 | Disk |
Am-17.1 | Amherst | 36 | 35 | 6 | 29 | 17.1 | Disk |
Ha-14.3 | Hadley | 36 | 35 | 5 | 30 | 14.3 | Disk |
Am-13.8 a | Amherst | 110 | 80 | 11 | 69 | 13.8 | Disk |
Among these seven cultivations, four sets were inoculated with activated sludge from the Amherst wastewater treatment plant (Amherst, MA), which operates at a solids retention time (SRT) of 10−15 days. The Amherst plant primarily receives municipal wastewater. The remaining three cultivations utilized activated sludge from the Hadley wastewater treatment plant, which employs a conventional activated sludge process with a 10 days SRT (Hadley, MA). The Hadley plant receives influent wastewater from residential, commercial, and agricultural sources. The measured initial water quality parameters and biomass characteristics of all cultivation sets are presented in Table 1. Each cultivation was named based on the source of the activated sludge and the percentage of vials in the cultivation that produced spheres. For example, “Am-100” indicates a cultivation using Amherst activated sludge that yielded only spheres, while “Ha-14.3” indicates a cultivation using Hadley activated sludge with 14.3% spheres, making it a disk-forming cultivation.
All aggregates exhibited an ellipsoidal shape in their final form, characterized by three perpendicular axes labeled as a, b, and c, corresponding to the radial length of the axes. By visual inspection, if an aggregate observed one semi-axis larger than the other two, it was considered a disk (Fig. 1). Otherwise, the aggregate's morphology was categorized as a sphere when all the semi-axes lengths were of equal length. Among the seven cultivation sets, three predominantly developed spherical photogranules in the remaining vials at the end of the cultivation period (Table 2). The cultivation set was labeled as either disk-forming or sphere-forming if 50% of the formed granules exhibited the same morphology. Spherical OPG formation was calculated as the ratio of the number of spherical OPGs to the total number of OPGs formed in each cultivation. Cultivations with 50% or more spherical OPG formation were classified as sphere-forming, while those with less than 50% were classified as disk-forming.
Fig. 1 Categorization of hydrostatic photogranules morphology based on semi-axes length. The left granule is an example of a disk, while the right granule is categorized as a sphere. |
In the Am-13.8 cultivation, out of 110 vials, 30 failed to aggregate into granules. The remaining vials successfully formed aggregates, with 13.8% resulting in spheres and the rest forming disks. In contrast, the Am-68.9 cultivation formed 119 aggregates out of 119 total vials, with a significant proportion of these aggregates adopting a spherical morphology (68.9%). After the cultivation period, ten vials containing formed disks from the Am-13.8 cultivation and twelve vials containing spherical aggregates from the Am-68.9 cultivation were randomly selected. These samples underwent vertical compression to quantitatively assess their mechanical and elastic properties.
Each OPG was transferred onto a submerged flat aluminum substrate under sterile conditions and subjected to compression loading using a GeoJac loading frame (Trautwein Soil Testing Equipment Inc.) equipped with a miniature load cell (Load Cell Central; Model EGC-50) with dimensions of 50 × 50 × 50 mm. The load cell was placed inside the acrylic glass enclosure within the loading frame to prevent air and dust disturbances. The loading cell had a capacity of 50 g (490 mN) and a resolution of 0.02 nM. Quasi-static loading was applied to individual OPGs at a constant displacement rate of 0.05 mm min−1 with unloading cycles. An image of the loading frame and load cell are depicted in Fig. S1 in ESI.†
As the OPGs exhibited various shapes, a nominal diameter, Do, was employed to normalize the size of OPGs.22
(1) |
The average diameter of a single OPG was calculated by averaging the lengths of the maximum, diagonal, and minimum radial lengths of the OPGs. Two-dimensional images of the OPGs were taken using a digital camera on the loading system to estimate the cross-sectional area and assumed a circular shape. To maintain consistency across measurements, a Vernier caliper with a precision of 0.02 mm was first used to measure the maximum, diagonal, and minimum lengths of the bottom surface of the OPGs. The average length of the bottom surface for each sample was then calculated from these measurements. Assuming the bottom surface is circular, this average length was used as the diameter to calculate the cross-sectional area of the sample. The Hertz elastic contact theory was applied to analyze the load-deformation curves, and the reduced modulus (Er) is reported as a measure of the contact stiffness between an OPG and the glass plate.23
(2) |
To identify the elastic stage beyond which the tested OPG started yielding, the Hertzian elastic contact line was determined by plotting 3P/D01/2versus d3/2 (as given in eqn (2)). The start of plastic yielding is marked by locating the point where the Hertz elastic contact line deviates from the experimental load-deformation curve. The yield shear stress, τy, of the OPG is then computed as:
(3) |
E = Er(1 − v2) | (4) |
Linearized two-parameter Weibull probability distributions (WPD) were employed to predict failure behavior regarding the mechanical properties of the OPGs in each cultivation. The Weibull cumulative distribution function was employed to model both E and τy of each tested OPG, described by the following equation.25
(5) |
(6) |
(7) |
Using eqn (7), the experimental data points can be fitted with eqn (6) to obtain k and b values through linear regression. These values then aid in determining the shape parameter λ with the following equation:
(8) |
Finally, the statistical mean value or characteristic value of extracted mechanical properties is determined using the gamma function:
(9) |
Extracellular polymeric substances (EPS) were extracted using the alkaline extraction method.29 Three randomly selected vials, each containing 10 mL, were destructively sampled. Subsequently, each individual vial was transferred to a sterile 50 mL centrifuge tube and centrifuged at 12000 rpm (20850 g) for 20 min at 4 °C. The supernatant, obtained after centrifugation, was collected and filtered through 0.45 μm cellulose filters to analyze the chemical composition of the soluble EPS fraction. Meanwhile, the remaining pellets were resuspended in 20 mL of phosphate buffer solution (10 mM NaCl, 1.2 mM KH2PO4, and 6 mM Na2HPO4).29 The buffer's conductivity was adjusted to replicate the conductivity of the activated sludge inoculum at a pH of 7.2.30 Each replicate underwent homogenization for 30 seconds. The pH of the homogenized samples was adjusted to pH 11 using 1 M NaOH and mixed on a shaker table at 400 rpm for 2 hours in the dark at 4 °C.30 A vial with only phosphate buffer adjusted to pH 11 with NaOH served as a blank control. Following extraction, each sample was centrifuged at 4 °C at 12000 rpm (20850 g) for 20 minutes. The supernatant was stored at −20 °C in aliquots until chemical analyses were conducted. Proteins (PN) and humic acids (HA) were measured using the modified Lowry method, and polysaccharides (PS) were measured as previously mentioned.29,31,32 Standards such as bovine albumin serum, humic acids, and glucose were employed for proteins, humic acids, and polysaccharides, respectively.
Principal component analysis (PCA) was performed on five out of the seven cultivations presented in this study to determine patterns in the data. For the PCA, the eigenvalues and proportion of variance for each principal component were determined using all 17 variables. The quality of variable representation was evaluated by calculating the square cosine values. The correlation analysis and PCA were all constructed using R.33
Mature photogranules from spherical cultivations, mainly Am-100 and Ha-100, exhibited lower Chl a concentration (5.97 ± 0.10 and 7.40 ± 0.38 mg L−1, respectively), compared to photogranules from disk cultivations with Chl a concentration ranging between 8.13–11.7 mg L−1. This suggests a higher phototrophic content in disk-shaped photogranules compared to spherical ones. The observed trend aligns with the notion that disk-shaped photogranules, with their slimmer thickness of approximately 3 mm, could potentially improve nutrient diffusion and light penetration, thereby enhancing the growth of phototrophic organisms. Based on the literature, the phototrophic outer layer developed in all statically formed photogranules is consistently around 500–1000 μm thick.1 Considering both sides of the disk granules, phototrophs can occupy approximately two-thirds of the entire thickness of the disk granules. Conversely, spherical photogranules, with a larger thickness ranging from 10 to 20 mm, might face challenges related to light and nutrient availability in the inner biomass layers. This situation could potentially restrict the growth of phototrophic organisms deeper within the granules. Based on the reported depth of the phototrophic layer in the literature, phototrophs in spherical granules can occupy only 10−20% of the entire granule thickness, which is significantly less compared to disk-shaped granules.1 This phenomenon aligns with established principles in microbial ecology, where structural attributes of granules play a pivotal role in modulating the microenvironment and subsequently influencing microbial community dynamics.34–36 The higher Chl a/b ratio in disk-shaped photogranules than in spherical ones suggests that the increase in phototrophic content was likely due to the higher cyanobacterial content in the disk-shaped photogranules.
EPS, a complex mixture of biopolymers secreted by cyanobacteria and other microbes, are known to enhance the cohesion and adhesion of cells, facilitating the formation and stability of photogranules.4Fig. 3 presents the concentrations of biomass-bound EPS during the granulation period for three cultivations: Ha-100 (sphere), Am-17.1 (disk), and Ha-14.3 (disk). Both EPS PN and HA exhibited decreasing trends over the initial 10−15 days of cultivation, followed by stabilization for both spherical and disk-like cultivations (Fig. 3a and c). The decreasing trend of EPS PN is common in hydrostatic granulation, as cyanobacteria have been reported to utilize EPS as a carbon source for their growth within photogranules.37 This ability gives cyanobacteria an advantage over other phototrophs, contributing to their dominance in the OPG biomass. EPS PS showed a minor increase for both spherical and disk-like cultivations and then stabilized or slightly decreased until the end of the cultivation period (Fig. 3b). The stability of EPS PS in spherical OPG cultivations aligns with findings from previous studies investigating hydrostatic photogranulation.3,4 In contrast, the PN/PS ratio decreased during the first 7 days of hydrostatic granulation and then stabilized (Fig. 3d).
Fig. 3 Changes in extracellular polymeric substances (EPS) concentrations during the granulation process. (A) Biomass-bound EPS proteins (PN), (B) biomass-bound EPS polysaccharides (PS), (C) humic acids (HA), and (D) PN/PS ratio. Data for the Ha-100 cultivation are reproduced from Kuo-Dahab et al. (2018).4 The solid line represents data from cultivations dominated by spherical granules, while the dashed lines represent data from cultivations dominated by disk-shaped granules. |
Compared to disk-shaped photogranules, spherical photogranules exhibited significantly lower concentrations of both EPS PN and EPS PS, suggesting improved granulation under the limitation of EPS. This finding aligns with previous hydrostatic photogranules studies, indicating that cyanobacteria granulate more effectively under the limitation of both EPS and Fe bound with EPS.3,12,38 Conversely, the PN/PS ratio of spherical photogranules was much higher than that of disk photogranules. The PN/PS ratio, indicating the proportion of hydrophobic to hydrophilic polymers in EPS, can offer insights into the settleability of granules. Hydrophilic constituents tend to exhibit enhanced settling capabilities by effectively integrating within the aqueous phase.39,40 Similar EPS transformation trends have also been reported in aerobic sludge granules, where granules exhibit higher PN concentrations than PS, resulting in PN/PS ratios of 1.4–1.6.41 EPS PN are found within the core of aerobic granules, contributing to increased granular stability due to enhanced internal hydrophobicity.41,42 In contrast, flocs have higher concentrations of PS, with PN/PS ratios closer to 0.5.41 Interestingly, the growth mechanism of small aerobic granules, similar to observations about OPGs, has been hypothesized to involve self-propagation rather than self-aggregation.1,3,4,43 In aerobic granules, this phenomenon is attributed to their reduced PN/PS ratios, leading to diminished hydrophobicity, a factor aiding granules in compacting during the granulation process.44
It is crucial to note that in the two cultivation sets Am-100 and Ha-100, which led to the development of spherical granules, observed decreases in the concentrations of DIN, NH4+, and NO3− during the initial week were sharp (Fig. 4). In contrast, the cultivation sets resulted in the formation of disk-shaped granules demonstrated increases or stability in both DIN and NH4+ within the initial days of operation, followed by rapid decreases. The observed elevation in NH4+ concentrations in these cultivation sets was likely attributed to biomass decay. Similar patterns for ammonium consumption have been observed for other hydrostatic granulation studies.3,9
It is also noteworthy that the three cultivations that showed initial DIN concentrations of less than 10 mg L−1 formed disk-shaped photogranules (Fig. 4). This finding aligns with Stauch-White et al.,9 who noted that cultivations with DIN concentrations below 9 mg L−1 did not yield spherical mature granules by the end of the granulation process.
In terms of nitrogen species, it appears that both ammonia and nitrate play essential roles in hydrostatic photogranulation. Ammonium is generally favored as a nitrogen source by most green algae and cyanobacteria compared to nitrate.49 This preference may explain the higher chlorophyll a concentrations observed in disk cultivations, where ammonia constitutes a significant fraction of the DIN, promoting rapid phototrophic proliferation. Nitrate (NO3−) might have been removed through biomass assimilation or denitrification (conversion of NO3− to N2). In aerobic granular sludge, denitrification was found to accelerate granule formation through two pathways: (1) the production of nitric oxide (NO) as an intermediate, known to induce cell aggregation and biofilm formation in bacterial cultures, and (2) generating alkalinity and creating conditions favorable for carbonate precipitation, which could provide nuclei for granulation and contribute to making the granules denser.50,51
First, we utilized a Spearman's correlation matrix to analyze the interactions among 17 selected parameters and their influence on OPG morphology, as shown in Fig. 5. It was found that phototrophic growth within photogranules, indicated by chlorophyll a, b, and c concentrations, exhibited positive correlations with both the initial DIN and ammonia concentrations in the cultivation vials. Among chlorophyll types, Chl a exhibited a strong positive correlation with NH4+ and a strong negative correlation with nitrate. This suggests that the abundance of phototrophs containing chlorophyll a but not b or c, such as cyanobacteria, are negatively correlated with initial nitrate concentrations. Diatoms and dinoflagellates, indicated by Chl c, demonstrated a strong positive correlation with DIN and a strong negative correlations with chloride (Cl−), magnesium (Mg2+), phosphate (PO4−3), potassium (K+), sulfate (SO42−), and sodium (Na+). Chl a also shows a strong negative correlation with sphere formation in comparison to Chl b and Chl c, which suggests that an initial lower abundance of phototrophs with chlorophyll a are linked to the formation of spherical OPGs.
On the other hand, OPG sphericity exhibited strong positive correlations (r > 0.6) with both the initial nitrate concentration in the soluble fraction and the total polysaccharide (TPS) concentration within biomass. This suggests that higher initial concentrations of nitrate and TPS are associated with a greater likelihood of preferential development of spherical OPGs. On contrary, OPG sphericity exhibited strong negative correlations with ammonium (NH4+), sodium, calcium (Ca2+), magnesium, phosphate (PO4−3) and sulfate (SO42−). Notably, sphere-forming cultivations AM-100 and Ha-100 commenced with initial PO4−3 concentrations below 2.1 mg P/L, while all disk cultivations had initial concentrations ranging between 3.0 mg P/L and 4.6 mg P/L.
The PCAbiplot, as depicted in Fig. 6, revealed distinct clusters based on the final morphology of OPGs. PCA effectively segregated two sphere cultivations in the upper left quadrants and the three disk cultivations in the lower right quadrants. The PCA biplot suggests a stronger correlation between the development of spherical OPGs with TPS and NH4+versus Chl a, Chl b, and Chl c. This suggests that the initial activated sludge characteristics, like EPS, may play an important role in the formation of spherical versus disk formation, as a large percentage of activated sludge biomass can be attributed to EPS or polysaccharides and proteins. The primary contributor to principal component 1 was Na+(11.0%), followed by SO42−(10.3%), Cl− (9.9%), Mg2+ (9.8%), DIN (8.6%) and K+ (8.3%) (Fig. S3†). Principal component 2 was influenced by TPS (16.4%), NH4+ (16.3%), tCOD (14.6%), VSS (12.4%), NO3− (9.5%), and PO43− (6.3%) (Fig. S4†). PC1 primarily measured inorganic ions found in activated sludge while PC2 measured biomass parameters and nutrients. PC1 accounts for 48.4% of proportion of variance, while PC2 accounts for 31.4%. The combined variance accounted for by both PC's is 79.8%. Out of these variables, 10 are considered water quality parameters (Cl−, K+, NO3−, Na+, NH4+, Ca2+, Mg2+, PO43−, SO42−, and DIN), while the remaining TPS, tCOD, and VSS are considered sludge biomass characteristics. The cultivation Am-100 (Sphere) lies on the PC1 axis which suggests it has a strong positive correlated with the initial inorganic ions. Cultivation Am-17.1 (disk) lies on the PC2 axis which suggest it has a strong positive correlation with initial biomass composition (TPS, tCOD, and VSS) and nutrients (NH4+, NO3−, and PO43−). This observations further suggests that while a multitude of factors may influence the formation of a specific granule morphology, the initial availability of nutrients can impact the rapid growth of cyanobacteria and lead to disk-shaped granules. The PCA highlights the importance of these specific water quality parameters and activated sludge characteristics in influencing photogranulation processes. Additionally, these factors could serve as valuable indicators of successful or unsuccessful photogranulation.
Fig. 6 Principal component analysis biplot depicting all 17 initial water quality variables from five OPG cultivations, with majority spheres represented in green and majority disks in blue. |
The distribution of light intensity for disk-shaped OPGs displayed a bimodal pattern, with each peak corresponding to a specific cultivation set, indicating similar densities. It is important to highlight that an increase in environmental temperature from 20 °C to 25 °C may lead to an increase in cyanobacterial growth.52 This is consistent with the optimal growth conditions for cyanobacterial species, which are often associated with higher temperatures (≥25 °C).53,54 While there seems to be a strong correlation between high localized temperatures and sphere formation, the growth of cyanobacteria is influenced by various factors, including the availability of inorganic nitrogen and phosphorus species, metal cations, COD, and photosynthetic activity, all of which play influential roles in determining the final morphology of OPGs.
The Weibull modulus estimates for both E and τy are presented in Table 3. Fig. S5† shows the Weibull distribution of the extracted mechanical properties (E, τy) for the two cultivations. All four cumulative WPD curves fit the supplied data linearly, with R2 values higher than the critical point R2 of 0.854 and 0.866 for Am-13.8 and Am-68.9 cultivations, respectively, which relates to a 95% confidence interval for small sample sets.
Am-13.8 (disks) | Am-68.9 (spheres) | ||
---|---|---|---|
Yield shear stress, τy | κ | 1.054 | 1.219 |
λ (kPa) | 0.605 | 0.452 | |
R 2 | 0.9557 | 0.8701 | |
Elastic modulus, E | κ | 1.272 | 1.127 |
λ (kPa) | 21.06 | 13.24 | |
R 2 | 0.8922 | 0.9546 |
All Weibull modulus values were close to or slightly greater than 1, indicating a constant rate of failure concerning either E or τy. This suggests that flaws within photogranule structure result from random failure, irrespective of the morphologies developed in different cultivations. In terms of τy, disk-like exhibited higher values than spherical photogranules (0.605 kPa vs. 0.452 kPa). This suggests that disk-like photogranules may exhibit greater resistance to deformation from shearing compared to spherical granules. This resistance could be attributed to the higher abundance of filamentous cyanobacteria in disk-like photogranules. Filamentous cyanobacteria are known for their high shear resistance due to the substantial thickness of their cell wall, reaching up to 500 nm.55–57
Additionally, disk-like (i.e., Am-13.8 cultivation) exhibited higher E values than spherical photogranules (i.e., Am-68.9 cultivation), 21.06 kPa compared to 13.24 kPa, indicating greater stiffness and greater capacity to withstand elevated stress levels before undergoing plastic deformation. The observed E values fall within the range observed in other biofilms, such as Pseudomonas aeruginosa grown on solid substrates, which demonstrated E values closer to 5−60 kPa.58 The higher stiffness of disk-dominated photogranules compared to spherical granules could be attributed to the increased EPS content within disk-dominated photogranules. In aerobic granular sludge, EPS are widely recognized as crucial contributors to microbial aggregation and play a key role in enhancing the compactness and mechanical stability of granules.1,59
The increased stiffness of disk-dominated photogranules can also be attributed to the higher initial concentrations of calcium (Ca2+) and magnesium (Mg2+) observed in their cultivation environment. This aligns with existing literature, which suggests that the stiffness of biofilms and cell aggregation is positively influenced by the availability of calcium and magnesium.47,58 Calcium and magnesium ions are known to crosslink alginate, which is a significant component of the extracellular polymeric substances produced by microbes in biofilms.47,60 Notably, alginate hydrogels, considered a reference material for investigating the mechanical properties of EPS, formed with Ca2+ cations, exhibited an E value of approximately 30 kPa, a similarity observed in OPGs from the Am-13.8 and Am-68.9 cultivations.47 Additionally, studies by Lin et al.61 demonstrated that the stiffness of aerobic granules increased with the number of crosslinks between alginate-like EPS and Ca2+ ions, resulting in a more robust gel structure than flocs. These findings suggest that hydrostatic OPGs form intricate networks of crosslinked biopolymers, facilitated by alkaline earth metals such as Mg and Ca. This process contributes to creating a stronger and stiffer material structure, with disk OPGs exhibiting notably higher strength and stiffness than their spherical counterparts.
Footnote |
† Electronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d4va00054d |
This journal is © The Royal Society of Chemistry 2024 |