首页> 外文期刊>Journal of Non-Crystalline Solids: A Journal Devoted to Oxide, Halide, Chalcogenide and Metallic Glasses, Amorphous Semiconductors, Non-Crystalline Films, Glass-Ceramics and Glassy Composites >Epoxide silylant agent ethylenediamine reaction product anchored on silica gel - thermodynamics of cation-nitrogen interaction at solid/liquid interface
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Epoxide silylant agent ethylenediamine reaction product anchored on silica gel - thermodynamics of cation-nitrogen interaction at solid/liquid interface

机译:固定在硅胶上的环氧硅烷化剂乙二胺反应产物-固/液界面上阳离子-氮相互作用的热力学

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摘要

The silylant agent 3-glycidoxypropyltrimethoxysilane has the epoxide ring opened by incorporating an ethylenediamine molecule under homogeneous conditions, to yield a new silylant agent, which is then anchored on silica gel. Based on nitrogen elemental analysis a large degree of immobilization gives 1.59 mmol g(-1), and consequently, a drastic decrease in surface area of the original silica from 420.8 +/- 3.4 to 70.6 +/- 0.5 m(2) g(-1) is observed for the immobilized surface. The basic centers attached on pendant groups have the capacity to extract cations from aqueous solution, whose adsorption process is adjusted to the Langmuir model. Similar profiles of adsorption were obtained on the isotherms with values 3.06, 2.91, 1.57 and 1.24 mmol g(-1) in the maximum of the curves for copper, cobalt, zinc and nickel, respectively. Thermodynamic data were obtained from calorimetric titration, indicating a spontaneity of these interactive reactions, caused by the favorable exothermic enthalpy due to the cation/basic center interaction in the solid/liquid interface and endothermic entropy originating from the increase in free water molecule content in the medium, which were displaced from the anchored surface, and the cation desolvation process, as the bond is formed. (C) 2003 Elsevier B.V. All rights reserved. [References: 24]
机译:甲硅烷基化剂3-环氧丙氧基丙基三甲氧基硅烷通过在均匀条件下掺入乙二胺分子而使环氧化物环开环,以产生新的甲硅烷基化剂,然后将其锚定在硅胶上。基于氮元素分析,高度固定化得到1.59 mmol g(-1),因此原始二氧化硅的表面积从420.8 +/- 3.4急剧下降至70.6 +/- 0.5 m(2)g(对于固定的表面观察到-1)。连接在侧基上的基本中心具有从水溶液中提取阳离子的能力,其吸附过程已根据Langmuir模型进行了调整。在等温线上获得了相似的吸附曲线,分别在铜,钴,锌和镍的最大曲线中的值为3.06、2.91、1.57和1.24 mmol g(-1)。从量热滴定获得热力学数据,表明这些相互作用的自发性是由于固/液界面中的阳离子/碱性中心相互作用以及由吸水的自由水分子含量增加引起的吸热熵引起的良好的放热焓所致。形成键的过程中,从锚固表面移开的介质和阳离子去溶剂化过程。 (C)2003 Elsevier B.V.保留所有权利。 [参考:24]

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