Issue 45, 2016

Unprecedented adsorptive removal of Cr2O72− and methyl orange by using a low surface area organosilica

Abstract

An extraordinary adsorption capacity of 359 and 1679 mg g−1 for the adsorptive removal of Cr2O72− and methyl orange (MO), respectively, was observed by using a low surface area (SABET of 10 m2 g−1) organosilica. The organosilica samples were synthesized by condensing phosphonitrilic chloride trimer with N1-3-(trimethoxysilylpropyl)ethylenetriamine followed by hydrolysis and co-condensation with different amounts of tetraethyl orthosilicate (TEOS). The kinetics, isotherms and thermodynamics of the adsorption process were investigated. The very high adsorption capacity of the low surface area adsorbent could be attributed to the formation of hemimicelles at the adsorbed sites of the adsorbent which suddenly increases the adsorption rate. An isotherm model was proposed similar to the adsorption model reported by Zhu and Gu with some modification. A pseudo-second order kinetic model fits best with the experimental data. Thermodynamically, as expected the present adsorption process is spontaneous and exothermic.

Graphical abstract: Unprecedented adsorptive removal of Cr2O72− and methyl orange by using a low surface area organosilica

Supplementary files

Article information

Article type
Paper
Submitted
14 Oct 2016
Accepted
26 Oct 2016
First published
27 Oct 2016

J. Mater. Chem. A, 2016,4, 17866-17874

Unprecedented adsorptive removal of Cr2O72− and methyl orange by using a low surface area organosilica

P. Rekha, R. Muhammad, V. Sharma, M. Ramteke and P. Mohanty, J. Mater. Chem. A, 2016, 4, 17866 DOI: 10.1039/C6TA08940B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements