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https://opaj.napstic.cn/periodicalArticle/downloadReview/0120160301987004
以不同官能化碳纳米管(原始MCN、氨基化AMCN和石墨化GMCN等)作为载体,通过浸渍法制备了Ru/CNTs催化剂,并应用于山梨醇氢解制1,2-丙二醇和乙二醇反应中. 利用XRD、HRTEM、XPS和ICP-AES等方法对催化剂进行了表征,考察了官能团性质、碱助剂等因素对山梨醇氢解性能的影响. 结果表明,与Ru/MCN或Ru/GMCN相比较,Ru/AMCN催化剂对山梨醇氢解有更高的活性,在205℃、5. 0 MPa氢压条件下,以Ca(OH)2 为添加剂,山梨醇的转化率可达99. 5%,1,2-丙二醇(1,2-PD)和乙二醇(EG)的总产率为47. 7%. 催化剂重复利用五次,催化活性无明显下降.
Ruthenium catalysts supported on carbon nanotubes with different functional groups ( MCN, AMCN and GMCN ) were prepared by incipient wetness impregnation with ultrasonic-assistance and used for the hydrogenolysis of sorbitol. The catalysts were characterized by X-ray diffraction ( XRD ) , HRTEM, X-ray photoelectron spectroscopy ( XPS) and ICP-AES. The effects of functional group species, and base additives on the catalytic performance of Ru/CNTs in the sorbitol hydrogenolysis reaction were investigated. Nearly 99. 5%of sorbitol conversion and 47 . 7% total yield of ethylene glycol and 1 , 2-propanediol ( 1 , 2-PD ) could be achieved over Ru/AMCN under mild reaction conditions (205℃, 5. 0 MPa), using Ca(OH)2 as additive. The conversion of sorbitol and the selectivity to ethylene glycol ( EG ) and 1 , 2-propanediol ( 1 , 2-PD ) did not decrease over the five repeated runs, which confirmed that the Ru/AMCN catalyst exhibited high stability in the aqueous hydrogenolysis of sorbitol to glycols.
董慧焕;郭星翠;秦张峰;韩生;牟新东
上海应用技术学院 化学与环境工程学院,上海 201418中国科学院青岛生物能源与过程研究所 生物基材料重点实验室,山东 青岛 266101中国科学院青岛生物能源与过程研究所 生物基材料重点实验室,山东 青岛 266101中国科学院山西煤炭化学研究所 煤转化国家重点实验室,山西 太原 030001中国科学院山西煤炭化学研究所 煤转化国家重点实验室,山西 太原 030001
化学
山梨醇氢解1,2-丙二醇乙二醇Ru/CNTs官能化
sorbitolhydrogenolysis12-propanediolethylene glycolRu/CNTsfunctionalization
《燃料化学学报》 2015 (12)
规整孔道限制的单一分散金属纳米粒子可控组装及糖醇氢解催化性能研究
1454-1460,7
The project was supported by the National Natural Science Foundation of China (21406251, 21201174) and the Foundation of State Key Laboratory of Coal Conversion (J13-14-603). 国家自然科学基金(21406251, 21201174)和煤转化国家重点实验室开放课题(J13-14-603)资助
https://opaj.napstic.cn/periodicalArticle/downloadReview/0120160301987004
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