journal article·2020-12

Creating Synergy of Microporous Hydrophilic–Organophilic Surfaces in Zeolite@Nano‐Titania Particles for Rapid Removal of Diverse Pollutants in Water

Ruchi Shaw, Shubhangi Madan, Sangeeta Tiwari, Sandeep Kumar Tiwari

Advanced Materials Interfaces· Volume 7· Issue 23
Publisher page

Abstract

Abstract The present work reports the synergy between microporous titania (hydrophilic surface) and zeolite (organophilic surface) through coating of nano‐titania particles in multilayers on zeolite (Ze) surface (Ze‐TiO2 core‐shell particles). The microporous hydrophilic shell, by virtue of its high wetting properties and van der Waals forces, attracts solvated analytes from water causing rapid diffusion across the solid–liquid interface. The stronger ionic/organophilic attraction by the core (zeolite) enables the pollutants from shell to migrate to the core leaving shell deficient for further adsorption. It establishes a continuous flow of analytes from bulk to the core through favorably charged hydrophilic layers of anatase TiO2 till the high‐capacity zeolite is completely adsorbed. Porous layers of TiO2 (shell) introduce rapid physiosorption of analytes while chemisorption mechanism is retained by zeolite core as confirmed by kinetic and isotherm studies on adsorption of heavy metal ion (Pb(II)) and organic dye (methylene blue). The mechanism of adsorption is substantiated by intraparticle diffusion model. The material holds promise as multifunctional adsorbent for rapid and efficient removal of diverse pollutants from water.
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Research context

OpenAlex topics: Adsorption and biosorption for pollutant removal · Nanomaterials for catalytic reactions · Analytical chemistry methods development

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Amity Institute of Applied Sciences Amity University Noida Uttar Pradesh 201303 India

Council of Scientific & Industrial Research New Delhi 110001 India

References (21)

Show source-provided references
1. 10.1002/cjoc.20150076110.1002/cjoc.201500761 ↗
2. 10.1016/j.jclepro.2017.12.05910.1016/j.jclepro.2017.12.059 ↗
3. 10.1016/j.jece.2016.02.00210.1016/j.jece.2016.02.002 ↗
4. 10.1016/j.ultsonch.2016.05.03610.1016/j.ultsonch.2016.05.036 ↗
5. 10.1016/j.cej.2009.10.02910.1016/j.cej.2009.10.029 ↗
6. 10.1021/acs.cgd.5b0146510.1021/acs.cgd.5b01465 ↗
7. 10.1039/C5EW00152H10.1039/C5EW00152H ↗
8. 10.1016/j.microc.2014.04.00110.1016/j.microc.2014.04.001 ↗
9. 10.1016/j.jece.2018.01.06310.1016/j.jece.2018.01.063 ↗
10. 10.1039/C5RA07994B10.1039/C5RA07994B ↗
11. 10.1088/0957-4484/26/22/22560310.1088/0957-4484/26/22/225603 ↗
12. 10.1016/j.jallcom.2010.06.07710.1016/j.jallcom.2010.06.077 ↗
13. 10.1016/j.tsf.2010.08.05110.1016/j.tsf.2010.08.051 ↗
14. 10.1039/c2cy00545j10.1039/c2cy00545j ↗
15. 10.1166/mex.2011.102110.1166/mex.2011.1021 ↗
16. 10.1016/j.micromeso.2005.05.04010.1016/j.micromeso.2005.05.040 ↗
17. 10.1016/j.apsusc.2013.12.15510.1016/j.apsusc.2013.12.155 ↗
18. 10.1021/acsami.6b0175410.1021/acsami.6b01754 ↗
19. 10.1016/j.saa.2017.02.00710.1016/j.saa.2017.02.007 ↗
20. Yan‐Li J · J. Environ. Sci. · 2006 · 18 · 158
21. 10.1016/j.jconrel.2004.04.00910.1016/j.jconrel.2004.04.009 ↗