Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/73038
Type: Artigo de periódico
Title: Useful aminoalcohol molecules incorporated in an epoxide silylating agent for silica organofunctionalization and thermodynamics of copper removal
Author: Melo, MA
Oliveira, FJVE
Sales, JAA
Airoldi, C
Abstract: Ethanolamine (E) and diethanolamine (D) molecules were incorporated onto a precursor 3-glycidoxypropyltrimethoxysilane (G) agent, followed by organofunctionalization of the silica gel through homogeneous (A) and heterogeneous (B) routes, to yield SiEA, wSiDA, SiEB and SiDB hybrids. These chemically organofunctionalized silicas were characterized by several techniques, including infrared spectroscopy (FTIR), solid-state nuclear magnetic resonance ((13)C and (29)Si NMR using CP/MAS), thermogravimetry and elemental analysis. Based on the obtained nitrogen percentages, the amount of pendant organic groups attached to the inorganic matrices SiEB, SiEA, SiDB and SiDA were calculated as 0.22 +/- 0.04, 1.05 +/- 0.03, 0.29 +/- 0.02 and 0.89 +/- 0.01, respectively. The infrared spectra presented characteristic bands attributed either to the inorganic framework or to the immobilized chains. Solid-state (13)C NMR results clearly demonstrated that the organic moieties are covalently bonded to the inorganic framework, while (29)Si NMR revealed the silicon atoms with distinct environments, Q and T, in agreement with the covalent attachment of organic moieties. The basic centers attached on the pendant groups have the ability to sorb copper from aqueous solution. This process was adjusted to the Langmuir model, to obtain maximum sorption values of 0.28 +/- 0.02, 0.40 +/- 0.02, 0.29 +/- 0.03, 0.76 +/- 0.02 mmol g(-1) for SiEB, SiEA, SiDB and SiDA hybrids, respectively, from the isotherms. Thermodynamic data obtained from calorimetric titrations reflected the spontaneity of the reactions, which are also enthalpically and entropically favorable for the proposed cation/basic center interactions for these chelating processes at the solid/liquid interface.
Country: Inglaterra
Editor: Royal Soc Chemistry
Rights: aberto
Identifier DOI: 10.1039/b822576a
Date Issue: 2009
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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