Zeolites as recyclable adsorbents/catalysts for biogas upgrading: Removal of octamethylcyclotetrasiloxane

被引:38
作者
Cabrera-Codony, Alba [1 ]
Georgi, Anett [2 ]
Gonzalez-Olmos, Rafael [1 ,3 ]
Valdes, Hector [4 ]
Martin, Maria J. [1 ]
机构
[1] Univ Girona, Inst Environm, LEQUIA, Campus Montilivi, E-17071 Girona, Catalonia, Spain
[2] UFZ Helmholtz Ctr Environm Res, Dept Environm Engn, Permoserstr 15, D-04318 Leipzig, Germany
[3] Univ Ramon Llull, IQS Sch Engn, Via Augusta 390, Barcelona, Spain
[4] Univ Catolica Santisima Concepcion, Lab Tecnol Limpias F Ingn, Alonso Ribera 2850, Concepcion, Chile
关键词
Siloxane; Zeolite; Fenton; Ozone; AOP; ACTIVATED CARBON; NATURAL ZEOLITE; ADSORPTION; SILOXANES; OXIDATION; CATALYSTS; SILICA; REGENERATION; PURIFICATION; DESORPTION;
D O I
10.1016/j.cej.2016.09.017
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Natural and synthetic zeolites with different properties (porous structure, SiO2/Al2O3 ratio, acidity and Fe-loading) were evaluated as adsorbents/catalysts for octamethylcyclotetrasiloxane (D4) removal in dynamic adsorption tests. BEA type zeolites, with high content of Lewis and Bronsted sites, promoted the catalytic D4 ring-opening leading on the formation of smaller alpha-omega-silanediols, which are narrower molecules able to diffuse into the channel system. Wet oxidation processes were used for the regeneration of a spent BEA zeolite, including ozonation and Fenton-like treatment. Both treatments were optimized to recover almost completely the D4 uptake of the iron-exchanged Fe-BEA in the first use. Thus, its feasibility to be reused was evaluated in successive adsorption/oxidation cycles, recovering up to 80% in at least three subsequent steps. However, in further cycles the accumulation of D4 and/or by-products led to a successive decline in the catalytic activity of the zeolites, hampering not only the capacity to transform D4 into lineal silanediols, thus reducing the adsorption capacity, but also the catalytic activity towards promoting Fenton-like reactions during regeneration. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:820 / 827
页数:8
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