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Type: Artigo de periódico
Title: Interaction of divalent copper with two diaminealkyl hexagonal mesoporous silicas evaluated by adsorption and thermochemical data
Author: Sales, JAA
Prado, AGS
Airoldi, C
Abstract: Hexagonal mesoporous silicas chemically modified with ethylenediamine moieties were synthesized through the co-condensation of tetraethylorthosilicate (TEOS) with two different silylating agents: (i) N-[3-(trimethoxysilyl)propyl]ethylenediamine and (ii) the new agent prepared from the incorporation of the ethylenediamine molecule into the epoxide group of the precursor 3-glycidoxypropyltrimethoxysilane. From these silylating agents under neutral n-octylamine template methodology, the respective MNN and MGNN inorganic-organic hybrids were synthesized. Elemental analysis showed that the number of pendant groups in these hybrids were 1.69 and 1.62 mmol g(-1), with pore diameters and surface areas of 1.81 and 1.53 nm and 663 +/- 14 and 614 +/- 16 m(2) g(-1). Infrared spectroscopy, nuclear magnetic resonance for C-13 and Si-29 nuclei and X-ray diffraction patterns are in agreement with the success of the proposed synthetic methods, as confirmed for the formation of the mesoporous hybrids. Both mesoporous materials have been used for divalent copper adsorption from aqueous solution at 298 I K. The series of adsorption isotherms were adjusted to a modified Langmuir equation. The maximum number of moles adsorbed gave 1.4 +/- 0.1 and 1.4 +/- 0.2 mmol g(-1) for MNN and MGNN, respectively. The same interactions were calorimetrically followed and gave exothermic enthalpy, negative Gibbs free energy and positive entropy values. These favorable thermodynamic data indicate cation/nitrogen basic center interactions on the new mesoporous materials at the liquid/solid interface for both systems. (c) 2005 Elsevier B.V. All rights reserved.
Subject: silicon
solid-liquid interface
porous solids
surface thermodynamics
compound formation
Country: Holanda
Editor: Elsevier Science Bv
Citation: Surface Science. Elsevier Science Bv, v. 590, n. 1, n. 51, n. 62, 2005.
Rights: fechado
Identifier DOI: 10.1016/j.susc.2005.06.007
Date Issue: 2005
Appears in Collections:Unicamp - Artigos e Outros Documentos

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