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作 者:Hongyan Li Hong Ma Xinhong Wang Jin Gao Chen Chen Song Shi Minjie Qu Na Feng Jie Xu
机构地区:[1]School of Textile and Material Engineering, Dalian Polytechnic University [2]State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences,Dalian National Laboratory for Clean Energy
出 处:《Journal of Energy Chemistry》2014年第6期742-746,共5页能源化学(英文版)
基 金:supported by the National Natural Science Foundation of China(21233008,21103175 and 20803074);the"Strategic Priority Research Program-Climate Change:Carbon Budget and Related Issues"of the Chinese Academy of Sciences(XDA05010203)
摘 要:Efficient catalytic oxidation of ethylbenzene to acetophenone was realized using the catalytic system of cobalt zeolitic imidazolate framework ZIF-67/N-hydroxyphthalimide (NHPI) under mild conditions. 95.2% conversion of ethylbenzene with 90.3% selectivity to acetophenone could be obtained at 373 K under 0.3 MPa 02 for 9 h. The results show that there exists synergetic effect between ZIF-67 and NHPI. 1-Phenylethyl hydroperoxide (PEHP) was generated via a radical process involving the hydrogen abstraction from ethylbenzene by phthalimide N-oxyl, and subsequently effectively decomposed to acetophenone by ZIF-67.Efficient catalytic oxidation of ethylbenzene to acetophenone was realized using the catalytic system of cobalt zeolitic imidazolate framework ZIF-67/N-hydroxyphthalimide (NHPI) under mild conditions. 95.2% conversion of ethylbenzene with 90.3% selectivity to acetophenone could be obtained at 373 K under 0.3 MPa 02 for 9 h. The results show that there exists synergetic effect between ZIF-67 and NHPI. 1-Phenylethyl hydroperoxide (PEHP) was generated via a radical process involving the hydrogen abstraction from ethylbenzene by phthalimide N-oxyl, and subsequently effectively decomposed to acetophenone by ZIF-67.
关 键 词:N-HYDROXYPHTHALIMIDE Z1F-67 OXIDATION ETHYLBENZENE ACETOPHENONE
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