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Hydrogen Production by Catalytic Steam Reforming of Bio-oil, Naphtha and CH4 over C12A7-Mg Catalyst 被引量:4
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作者 Yue Pan Zhao-xiang Wang +2 位作者 Tao Kan xi-feng zhu Quan-xin Li 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 北大核心 2006年第3期190-192,共3页
Hydrogen production by catalytic steam reforming of the bio-oil, naphtha, and CH4 was investigated over a novel metal-doped catalyst of (Ca24Al28O64)^4+·4O^-/Mg (C12A7-Mg). The catalytic steam reforming was ... Hydrogen production by catalytic steam reforming of the bio-oil, naphtha, and CH4 was investigated over a novel metal-doped catalyst of (Ca24Al28O64)^4+·4O^-/Mg (C12A7-Mg). The catalytic steam reforming was investigated from 250 to 850℃ in the fixed-bed continuous flow reactor. For the reforming of bio-oil, the yield of hydrogen of 80% was obtained at 750℃, and the maximum carbon conversion is nearly close to 95% under the optimum steam reforming condition. For the reforming of naphtha and CH4, the hydrogen yield and carbon conversion are lower than that of bio-oil at the same temperature. The characteristics of catalyst were also investigated by XPS. The catalyst deactivation was mainly caused by the deposition of carbon in the catalytic steam reforming process. 展开更多
关键词 C12A7-Mg BIO-OIL NAPHTHA CH4 Catalytic steam reforming HYDROGEN
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Synthesis and structure-activity relationships study ofα-aminophosphonate derivatives containing a quinoline moiety 被引量:1
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作者 xi-feng zhu Jing Zhang +3 位作者 Shuo Sun Yan-Chun Guo Shu-Xia Cao Yu-Fen Zhao 《Chinese Chemical Letters》 SCIE CAS CSCD 2017年第7期1514-1518,共5页
Two series of a-aminophosphonate derivatives containing a quinoline moiety have been designed and synthesized by introducing bioactive quinoline scaffold to a-aminophosphonate. The in vitro cytotoxic activities of tar... Two series of a-aminophosphonate derivatives containing a quinoline moiety have been designed and synthesized by introducing bioactive quinoline scaffold to a-aminophosphonate. The in vitro cytotoxic activities of target compounds were first investigated against two human cancer cell lines including Eca109 and Huh7 by MTT assay. Results revealed that most of target compounds exhibited moderate to high antitumor activities against the tested cancer cell lines and some demonstrated more potent inhibitory activities compared with Sunitinib. Among them, compounds 4b2 and 4b4 containing methylsubstituted aniline group were found to be more active than Sunitinib against both of two cancer cell lines, with IC50 in the range of 2.26 mmol/L–7.46 mmol/L. 展开更多
关键词 Quinoline a-Aminophosphonate Synthesis Antitumor activity In vitro
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