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Photocatalytically reducing CO2 to methyl formate in methanol over ZnS and Ni-doped ZnS photocatalysts

机译:ZnS和Ni掺杂的ZnS光催化剂上光催化将CO2还原为甲醇中的甲酸甲酯

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摘要

A series of ZnS photocatalysts were prepared via simple precipitation, ion-exchange and hydrothermal methods, respectively; meanwhile, various Ni-doped ZnS photocatalysts were synthesized by hydrothermal method. The obtained photocatalysts were characterized by XRD, UV-Vis, BET and SEM, and used for photocatalytically reducing CO2 to produce methyl formate in methanol, which worked as both solution of absorbing CO2 and sacrificial reagent. Under the analysis of an on-line ATR-FT1R spectroscopy for CO2 in methanol and detection of GC for the products, the experimental results showed that the ZnS photocatalysts prepared by hydrothermal method had higher photocatalytic activity, which increased rapidly with the increasing hydrothermal time and reached a maximum at 24 h. Besides, the doping of Ni~(2+) could further enhance this activity, the optimal content of Ni dopant was about 0.3 wt% and the corresponding methyl formate production rate was 121.4 μmol g~(-1) h~(-1). The high photocatalytic activity could be attributed to that the Ni~(2+) doping facilitated the separation of photogenerated electron-hole pairs and reduced their recombination probability.
机译:分别通过简单的沉淀法,离子交换法和水热法制备了一系列的ZnS光催化剂。同时,通过水热法合成了各种掺Ni的ZnS光催化剂。用XRD,UV-Vis,BET和SEM对所得的光催化剂进行了表征,用于光催化还原CO2,生成甲醇中的甲酸甲酯,作为吸收CO2的溶液和牺牲剂。通过对甲醇中CO2的在线ATR-FT1R光谱分析和产物的GC检测,实验结果表明,水热法制备的ZnS光催化剂具有较高的光催化活性,并随着水热时间的增加而迅速增加。在24小时达到最大值。此外,Ni〜(2+)的掺杂可进一步增强该活性,Ni掺杂剂的最佳含量约为0.3 wt%,相应的甲酸甲酯生成率为121.4μmolg〜(-1)h〜(-1) 。 Ni〜(2+)的掺杂促进了光生电子-空穴对的分离并降低了它们的复合概率,因此具有较高的光催化活性。

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