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Hydrogenase as the basis for green hydrogen production and utilization
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作者 Haishuo Ji Lei Wan +8 位作者 Yanxin Gao Ping Du Wenjin Li Hang Luo Jiarui Ning Yingying Zhao Huangwei Wang Lixin Zhang Liyun Zhang 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2023年第10期348-362,I0011,共16页
Hydrogenase is a paradigm of highly efficient biocatalyst for H_(2) production and utilization evolved in nature. A dilemma is that despite the high activity and efficiency expected for hydrogenases as promising catal... Hydrogenase is a paradigm of highly efficient biocatalyst for H_(2) production and utilization evolved in nature. A dilemma is that despite the high activity and efficiency expected for hydrogenases as promising catalysts for the hydrogen economy, the poor oxygen tolerance and low yield of hydrogenases largely hinder their practical application. In these years, the enigmas surrounding hydrogenases regarding their structures, oxygen tolerance, mechanisms for catalysis, redox intermediates, and proton-coupled electron transfer schemes have been gradually elucidated;the schemes, which can well couple hydrogenases with other highly efficient(in)organic and biological catalysts to build novel reactors and drive valuable reactions, make it possible for hydrogenases to find their niches. To see how scientists put efforts to tackle this issue and design novel reactors in the fields where hydrogenases play crucial roles, in this review,recent advances were summarized, including different strategies for protecting enzyme molecules from oxygen, enzyme-based assembling systems for H_(2) evolution in the photoelectronic catalysis, enzymatic biofuel cells for H_(2) utilization and storage and the efficient electricity-hydrogen-carbohydrate cycle for high-purity hydrogen and biofuel automobiles. Limitations and future perspectives of hydrogenasebased applications in H_(2) production and utilization with great impact are discussed. In addition, this review also provides a new perspective on the use of biohydrogen in healthcare beyond energy. 展开更多
关键词 hydrogenase Biological h_(2)energy Oxygen tolerance Artificial photosynthesis Biofuel cells
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含膦配体二铁二硫五羰基配合物的合成、表征及电催化产氢性能 被引量:2
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作者 刘旭锋 徐博 +1 位作者 徐航 李玉龙 《无机化学学报》 SCIE CAS CSCD 北大核心 2023年第8期1619-1627,共9页
本文报道了4个含膦配体二铁二硫五羰基配合物的合成和结构表征。起始配合物[Fe_(2)(CO)_(6)(μ-SCH_(2)CH(CH_(2)OOCH)S)](1)与三苯基膦、三环己基膦、三(2-甲氧基苯基)膦或三(4-三氟甲基苯基)膦和脱羰试剂Me3NO·2H_(2)O反应,以59%... 本文报道了4个含膦配体二铁二硫五羰基配合物的合成和结构表征。起始配合物[Fe_(2)(CO)_(6)(μ-SCH_(2)CH(CH_(2)OOCH)S)](1)与三苯基膦、三环己基膦、三(2-甲氧基苯基)膦或三(4-三氟甲基苯基)膦和脱羰试剂Me3NO·2H_(2)O反应,以59%~88%的产率制备了目标产物[Fe_(2)(CO)_(5)(L)(μ-SCH_(2)CH(CH_(2)OOCH)S)](L=PPh_(3)(2)、PCy_(3)(3)、P(2-C_(6)H_(4)OCH_(3))_(3)(4)、P(4-C_(6)H_(4)CF_(3))_(3)(5))。配合物2~5以元素分析、红外光谱、核磁共振以及单晶X射线衍射进行了表征。电化学性质研究表明配合物1~5均可以实现电化学催化质子还原产生氢气的功能,其中配合物1的催化产氢效率明显优于其它配合物。 展开更多
关键词 铁铁氢化酶 双铁配合物 X射线晶体学 产氢催化剂
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紫云英根瘤菌109菌株吸氢特性及碳底物的调节 被引量:1
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作者 孙金华 陈秉俭 宋鸿遇 《植物生理学报(0257-4829)》 CSCD 1989年第4期382-387,共6页
紫云英根瘤菌109菌株完整细胞的吸氧活性,在空气气相中衰减快,加氢或降低温度,衰减延缓。完整细胞的吸氢反应受体,包括甲基蓝、氧、铁氰化钾、TTC、甲基紫精、Cyt C_3、硝酸钾、DCPIP和反丁烯二酸盐的表现不相同。当氧为受体时,气相氧... 紫云英根瘤菌109菌株完整细胞的吸氧活性,在空气气相中衰减快,加氢或降低温度,衰减延缓。完整细胞的吸氢反应受体,包括甲基蓝、氧、铁氰化钾、TTC、甲基紫精、Cyt C_3、硝酸钾、DCPIP和反丁烯二酸盐的表现不相同。当氧为受体时,气相氧浓度为5%,吸氢值最大,甲基蓝为受体时,吸氢活性高。另外,氧为受体的吸氢受到碳水化合物抑制,并与基础吸氧速率相关。紫云英根瘤菌的氢氧化与碳水化合物氧化竞争电子传递途径。 展开更多
关键词 紫云英 根瘤菌 吸氢活性 调节 氢酶
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水稻根际兼性厌氧催娩克氏杆菌和阴沟肠杆菌的固氮与氢代谢
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作者 孙金华 陈秉俭 +1 位作者 杨玉锁 宋鸿遇 《植物生理学报(0257-4829)》 CSCD 1991年第4期380-388,共9页
兼性厌氧细菌Enterobacter cloacae菌株E-26和Klebsiella oxytoca菌株NG-13的氢酶与固氮酶同时形成。固氮的最佳碳源为蔗糖、葡萄糖和丙酮酸,此外延胡索酸和苹果酸也能支持固氮。支持固氮的碳源也支持放氢,两者动力学基本一致。40%乙... 兼性厌氧细菌Enterobacter cloacae菌株E-26和Klebsiella oxytoca菌株NG-13的氢酶与固氮酶同时形成。固氮的最佳碳源为蔗糖、葡萄糖和丙酮酸,此外延胡索酸和苹果酸也能支持固氮。支持固氮的碳源也支持放氢,两者动力学基本一致。40%乙炔预处理后,吸氢活性下跌,放氢量未增加;NH_4^+抑制固氮酶,但未导致放氢量降低;可能E-26菌株的放氢主要依赖于氢酶。菌株E-26和NG-13的吸氢反应,既能以O_2为电子受体,也能以延胡索酸、硝酸、MB为电子受体。但仅延胡索酸为电子受体时,E-26菌的固氮活性被分子H_2促进,它的氢吸收利用与固氮相偶联;而在CO_2和NH_4^+代谢与H_2利用之间并无明显相关性,吸氢活性不被CO_2和NH_4^+促进。 展开更多
关键词 水稻 固氮 代谢 催娩克氏杆菌
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