Optimisation of sepiolite clay with phosphoric acid treatment as support material for CoB catalyst and application to produce hydrogen from the NaBH4 hydrolysis

被引:67
作者
Selvitepe, Nuran [1 ]
Balbay, Asim [1 ]
Saka, Cafer [2 ]
机构
[1] Siirt Univ, Fac Engn, TR-56100 Siirt, Turkey
[2] Siirt Univ, Sch Hlth, TR-56100 Siirt, Turkey
关键词
Sepiolite; Phosphoric acid; Modification; NaBH4; Hydrogen; SODIUM-BOROHYDRIDE; COBALT(0) NANOCLUSTERS; GENERATION; PALYGORSKITE; EFFICIENT; KAOLIN; SILICA; ADSORPTION; REACTIVITY; COST;
D O I
10.1016/j.ijhydene.2019.04.254
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Herein, the CoB catalyst supported on the sepiolite clay treated with phosphoric acid was utilized to produce hydrogen from the NaBH4 hydrolysis. In order to analyse the performance of the phosphoric acid treated sepiolite clay supported-CoB catalyst, the NaBH4 concentration effect, phosphoric acid concentration effect, phosphoric acid impregnation time effect, CoB catalyst percentage effect, and temperature effect were studied. In addition, XRD, XPS, SEM, TEM, BET, and FTIR analysis were performed for characterization of Co-B catalyst supported on the acid-treated sepiolite. The completion time of this hydrolysis reaction with Co-B (20%) catalyst supported on the sepiolite treated by 5 M phosphoric acid was approximately 80 min, whereas the completion time of this hydrolysis reaction with acid-free sepiolite-supported Co-B (20%) catalyst was approximately 260 min. There is a five-fold increase in the maximum production rate. The maximum hydrogen production rates of this hydrolysis reaction at 30 and 60 degrees C were found as 1486 and 5025 ml min(-1)g(catalyst)(-1), respectively. Activation energy was found as 21.4 kJ/mol. This result indicates that the acid treatment on sepiolite is quite successful. The re-usability of NaBH4 hydrolysis reaction by CoB catalyst supported on sepiolite treated phosphoric acid for successive five cycles of NaBH4 at 30 degrees C was investigated. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:16387 / 16399
页数:13
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