109
Views
11
CrossRef citations to date
0
Altmetric
Original Articles

Functionalized SiO2 With S-Donor Thiophene: Synthesis, Characterization, and Its Heavy Metals Adsorption

&
Pages 2003-2013 | Received 10 Sep 2009, Accepted 25 Oct 2009, Published online: 24 Sep 2010
 

Abstract

Porous silica has been chemically modified with thiophene using the heterogeneous route. This synthetic route involved the reaction of native silica, SiO2, with a commercial silylating agent, 3-glycidoxypropyltrimethoxysilane, followed by the immobilization of the thiophene chelating groups on the support. The resulting material has been characterized by thermogravimetry, FTIR spectra, and elemental analysis. The solid was also studied and evaluated by determination of the surface area using the BET equation, and the adsorption and desorption capability using the isotherm of nitrogen and B.J.H. pore sizes. The new synthesized material was employed in a batch method as adsorbent from aqueous solutions of Hg2+, Cd2+, Pb2+, Cu2+, Zn2+, K+, Na+, and Li+.

Notes

a So: native silica.

b Solid–liquid extraction of individual cations using MSiTh.

c Solid–liquid extraction in competitive mode using MSiTh.

d Kd: The distribution ratio of the metal ion in competitive adsorption (mL/g).

e Ki: A selectivity coefficient for the binding of Hg2+ in competitive adsorption.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.