4.7 Article

Surface functionalization of SBA-15 and a nonordered mesoporous silica with a 1,4-diazabicyclo[2.2.2]octane derivative: Study of CuCl2 adsorption from ethanol solution

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 356, 期 1, 页码 248-256

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2010.12.030

关键词

SBA-15; Mesoporous silica; DABCO; Adsorbents; Ethanol purification

资金

  1. CNPq
  2. FAPESP

向作者/读者索取更多资源

This work describes the preparation and characterization of postfunctionalized ordered (SBA-15) and nonordered (SMD) mesoporous silicas with n-propyl-1,4-diazoniabicycle[2.2.2]octane chloride (DbCl) moiety. The main interest is based on the fact that these materials are excellent adsorbents due to the ability of functional groups to retain copper chlorides on their surfaces as anionic complexes CuCl2+nn-. The specific surface areas (S-BET) and average pore diameters (d(pore)) for SBA-15 and SMD are SBA-15, S-BET = 944 m(2) g(-1), d(pore) = 9.0 nm; SMD, S-BET = 710 m(2) g(-1), d(pore) = 11 nm. On functionalization with DbCl, reductions in the specific surface areas of the resulting materials (SBA-15/DbCl and SMD/DbCl) are observed and the following functionalization degrees (phi) were determined: SBA-15/DbCl, S-BET = 247 m(2) g(-1), phi = 0.95 mmol g(-1); SMD/DbCl, S-BET = 83 m(2) g(-1), phi = 1.2 mmol g(-1). The adsorption equilibria of CuCl2 in ethanol were characterized, and the heterogeneous stability constants, beta(1) and beta(2), corresponding to formation of CuCl42- and CuCl3- anionic species adsorbed on the surface were found. Also, the effective sorption capacities (t(Q)) were determined: SBA-15/DbCl, log beta(1) = 4.46, log beta(2) = 7.10, t(Q) = 0.80 mmol g(-1); SMD/DbCl, log beta(1) = 4.95, log beta(2) = 7.52, t(Q) = 0.75 mmol g(-1). Regeneration of the adsorbents requires a very simple procedure consisting of their immersion in aqueous solution followed by immediate release to the solution phase of the Cu(OH2)(n)(2+) species, followed by chloride anions as the counterions. (C) 2011 Published by Elsevier Inc.

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