ON THE INTERACTION OF THIOPHENE AND ZEOLITE-Y IN THE THIOPHENE-BASED OLIGOMERS FORMATION

被引:0
|
作者
Rivera, V. M. [1 ]
Suarez-Mendez, A. [1 ]
Pascual-Mathey, L., I [2 ]
Gutierrez, A. [3 ]
Vera, M. A. [3 ]
Fuentes, G. A. [4 ]
机构
[1] Univ Veracruzana, Fac Ciencias Quim, Xalapa 91000, Veracruz, Mexico
[2] Univ Veracruzana, Fac Quim Farmaceut Biol, Xalapa 91000, Veracruz, Mexico
[3] Univ Autonoma Metropolitana Iztapalapa, Lab Resonancia Magnet Nucl, Ciudad De Mexico 09340, Mexico
[4] Univ Autonoma Metropolitana Iztapalapa, Dept Ing Proc & Hidraul, Ciudad De Mexico, Mexico
来源
关键词
Thiophene; zeolite Y; Bronsted acid sites; oligomers; DEEP HYDRODESULFURIZATION; DESULFURIZATION; ADSORPTION; FUELS; DEACTIVATION; SORBENTS; CRACKING;
D O I
暂无
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Due to the inconsistencies in the literature about the structure of thiophene oligomers, formed by the interaction between thiophene and the Bronsted acid sites of zeolite Y, the direct analysis of these oligomeric species is fundamental, mainly to understand how they are made up and their correct structure. The materials used were zeolite Y in its protonic (HY) and sodic (NaY) form. The interaction between thiophene and the zeolitic material was performed by the adsorption of thiophene at room temperature using a solution of thiophene in n-octane (100-700 ppmw), leading to the formation of cationic thiophene oligomers that are trapped inside the cavities of HY, among other non-oligomeric species. The thiophene-zeolite Y interaction occurs through the Bronsted acid sites by two possible routes: i) by electrophilic attack to the pair of free electrons in sulfur, forming oligothiophene whose size is limited by the structure of zeolite and, ii) by interaction with the alpha-carbon that leads to the formation of H2S, thiols and hydrocarbons with carbons with sp(3) hybridization.
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页码:471 / 479
页数:9
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