首页> 外文期刊>Journal of the Japan Petroleum Institute >Local Structure Analysis of Active Sites in NiO/γ-Al2O3 Catalyst for Dimethyl Sulfide Decomposition: Sulfurization Behavior of Ni Species Using X-ray Absorption Spectroscopy Analysis
【24h】

Local Structure Analysis of Active Sites in NiO/γ-Al2O3 Catalyst for Dimethyl Sulfide Decomposition: Sulfurization Behavior of Ni Species Using X-ray Absorption Spectroscopy Analysis

机译:Nio /γ-Al2O3催化剂中活性位点的局部结构分析,用于二甲基硫化物分解:Ni种类使用X射线吸收光谱分析的硫化行为

获取原文
           

摘要

Local structures of Ni species were studied in the NiO/γ-Al 2 O 3 catalyst prepared by the impregnation method for the decomposition of dimethyl sulfide (DMS). Calcination and sulfurization conditions of the prepared catalyst affected the catalytic activity for DMS decomposition. The decomposition performance was increased with sulfurization by H 2 S compared to sulfurization with DMS prior to the reaction test. X-ray diffraction and X-ray photoelectron spectroscopy analyses indicated that the active sites are NiS. Furthermore, in-situ X-ray absorption spectroscopy analysis was conducted to investigate the fine structural changes of Ni species before and after the sulfurization treatment. For the catalyst calcined at 500 °C, Ni species were present as NiO and NiAl 2 O 4 at a ratio of ca. 4 : 6 and only NiO was sulfurized to NiS which acts as the active sites. In contrast, for the catalyst calcined at 800 °C, Ni species were almost completely present as the Ni component in the NiAl 2 O 4 structure, which is less susceptible to sulfurization than NiO. Therefore, the NiS amount in the catalyst calcined at 800 °C was significantly reduced, leading to lower decomposition activity.
机译:研究了Ni /γ-Al 2 O 3催化剂中的Ni物种的局部结构,用于通过浸渍方法用于分解二甲基硫醚(DMS)。制备催化剂的煅烧和硫化条件影响了DMS分解的催化活性。在反应试验之前将H 2 S与H 2 S硫化的分解性能增加。 X射线衍射和X射线光电子能谱分析表明活性位点是NIS。此外,进行了原位X射线吸收光谱分析,以研究硫化处理前后Ni种类的细结构变化。对于在500℃下煅烧的催化剂,Ni物种以Ca的比例作为NiO和Nial 2 O 4存在。 4:6只有NIO硫化至NIS,其充当活性位点。相反,对于在800℃下煅烧的催化剂,Ni物种几乎完全存在于Nial 2 O 4结构中的Ni组分,其比NiO更易于硫化。因此,在800℃下煅烧的催化剂中的NIS量显着降低,导致分解活性降低。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号