Preparation and characterization of hydrophilic organo-montmorillonites through incorporation of non-ionic polyglycerol dendrimers derived from soybean oil

被引:30
作者
Azzouz, Abdelkrim [1 ]
Nousir, Saadia [1 ]
Platon, Nicoleta [1 ,2 ]
Ghomari, Kamel [1 ,4 ]
Hersant, Gregory [3 ]
Bergeron, Jean-Yves [3 ]
Shiao, Tze Chieh [1 ]
Rej, Rabindra [1 ]
Roy, Rene [1 ]
机构
[1] Univ Quebec, Dept Chem, Nanoqam, Succ Ctr Ville, Montreal, PQ H3C 3P8, Canada
[2] Bacau Univ, Catalysis & Microporous Mat Lab, RO-5500 Bacau, Romania
[3] Oleotek, Thetford Mines, PQ G6G 0A5, Canada
[4] Oran Es Senia Univ, Mat Chem Lab, El Mnaouer, Algeria
关键词
Composites; Layered compounds; Microporous materials; Nanostructures; Surface properties; CARBON-DIOXIDE; RETENTION; GASES; ADSORPTION; SURFACTANT;
D O I
10.1016/j.materresbull.2013.05.043
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Na-montmorillonite modification by the incorporation of hyperbranched polyglycerol dendrimers with average molecular weight 500, 1100 and 1700 g/mol and derived from soybean oil resulted in hybrid matrices with improved hydrophilic character and affinity toward carbon dioxide. Thermal analyses and thermal programmed desorption revealed that the dendrimer incorporation improved the amount of adsorbed water. The hydration grade was found to be proportional to the number of OH groups incorporated, and can double with the insertion of polyglycerol 500, 100 and 1700 at low dendrimer loadings. Inversely, higher dendrimer contents appeared to affect the hydrophilic character, favoring dendrimer aggregation into dense clusters, which reduces the number of OH groups accessible. This phenomenon was more accentuated with larger dendrimers. FTIR investigations also demonstrated that polyglycerol-based organoclays display improved interactions with water and/or carbon dioxide as compared to the starting material. The amount of adsorbed water was found to correlate with that of carbon dioxide, suggesting a certain contribution in CO2 retention. Crown Copyright (C) 2013 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3466 / 3473
页数:8
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