Dehydrogenation of methylcyclohexane over Pt-based catalysts supported on functional granular activated carbon

被引:19
|
作者
Ye, Hong-Li [1 ,2 ]
Liu, Shuang-Xi [2 ,3 ]
Zhang, Cui [2 ,3 ]
Cai, You-Qiong [1 ]
Shi, Yong-Fu [1 ]
机构
[1] Chinese Acad Fishery Sci, East China Sea Fisheries Res Inst, Lab Aquat Prod Qual Safety & Proc, Shanghai 200090, Peoples R China
[2] Nankai Univ, Sch Mat Sci & Engn, Inst New Catalyt Mat Sci, MOE Key Lab Adv Energy Mat Chem,Natl Inst Adv Mat, Tianjin 300350, Peoples R China
[3] Collaborat Innovat Ctr Chem Sci & Engn, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
SULFONIC-ACID GROUPS; NITROGEN-DOPED CARBON; HYDROGEN-PRODUCTION; TECHNOECONOMIC ANALYSIS; SILICON NANOPARTICLES; EFFICIENT; EVOLUTION; DOTS; CYCLOHEXANE; PERFORMANCE;
D O I
10.1039/d1ra05480e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we developed the dehydrogenation of methylcyclohexane over Pt-based catalysts supported on functional granular activated carbon. Sulphuric acid, hydrogen peroxide, nitric acid and aminopropyl triethoxy silane were adopted to modify the granular activated carbon. The structural characterizations suggested that the carbon materials had a large surface area, abundant pore structure, and a high number of oxygen-containing functional groups, which influenced the Pt-based catalysts on the particle size, dispersion and dehydrogenation activity. The hydrogen temperature-programmed reduction technique was utilized to investigate the interaction between the active component Pt and the various functionalized granular activated carbon materials. The CO pulse technique revealed the particle sizes and dispersion of the as-prepared Pt-based catalysts. Finally, the Pt-based catalysts were successfully applied to study their catalytic activity in the dehydrogenation reaction of methylcyclohexane. The results showed that the Pt-based catalyst over granular activated carbon functionalized with sulphuric acid groups had a higher conversion of methylcyclohexane (63%) and a larger hydrogen evolution rate (741.1 mmol g(Pt)(-1) min(-1)) than the other resulting Pt-based catalysts at 300 degrees C.
引用
收藏
页码:29287 / 29297
页数:11
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