...
首页> 外文期刊>Journal of Catalysis >Deuterium tracer studies on hydrotreating catalysts. 2. Contribution of the hydrogen of the alumina support to H-D exchange
【24h】

Deuterium tracer studies on hydrotreating catalysts. 2. Contribution of the hydrogen of the alumina support to H-D exchange

机译:氘示踪剂对加氢处理催化剂的研究。 2.氧化铝载体的氢对H-D交换的贡献

获取原文
获取原文并翻译 | 示例
           

摘要

H-D isotopic exchange between H-2 and D-2 was carried out at 80 degrees C in a recycling reactor under a pressure of 2 bar over unsupported MoS2 as well as on alumina supported Mo or NiMo sulfide catalysts. H-2-D-2 experiments carried out over a commercial NiMo/Al2O3 catalyst, to which were mixed different amounts of the alumina support, and over a series of Mo/Al2O3 catalysts containing different amounts of Mo (4.4 to 14.8 wt%) showed that part of the exchangeable hydrogen detected by isotopic dilution came from the added alumina or from the support. This amount of hydrogen on the alumina was estimated for each series, to be respectively 22.1 x 10(-4) and 17.8 x 10(-4) mol H . g(-1). Since under the same conditions H-D exchange between H-2 and D-2 did not occur at an appreciable rate on the alumina alone, it is concluded that hydrogen atoms from structural hydroxyl groups of the alumina or from hydroxyl groups resulting from the dissociation of H2S were able to migrate from grain to grain and to exchange with H-2 (D-2) dissociated on the sulfide active phase. The hydrogen atoms supposedly migrate as protons by jumping from oxygen to oxygen atoms on the alumina surface or are conveyed through the gas phase by H2S (the "shuttle molecule") which can adsorb dissociatively both on the alumina support and on the active phase. D-2 adsorption followed by FTIR under similar conditions confirmed that the presence of the sulfide phase was necessary, under the conditions of the experiments, to make the isotopic exchange between H-2 (D-2) in the gas phase and the hydroxyls of the alumina possible. OD bands were difficult to detect on sulfided alumina alone, even after 5 h of exposure to D-2, whereas a strong OD band appeared very rapidly on sulfided NiMo/Al2O3. These results are considered as being in favour of a heterolytic splitting of H-2 On sulfide catalysts. (C) 1998 Academic Press. [References: 37]
机译:H-2和D-2之间的H-D同位素交换是在循环反应器中于80摄氏度,2 bar的压力下,在未负载的MoS2上以及在氧化铝负载的Mo或NiMo硫化物催化剂上进行的。 H-2-D-2实验是在商用NiMo / Al2O3催化剂上进行的,在其中混合了不同量的氧化铝载体,并在一系列包含不同量Mo(4.4-14.8 wt%)的Mo / Al2O3催化剂上进行了实验结果表明,通过同位素稀释检测到的部分可交换氢来自添加的氧化铝或载体。对于每个系列,估计氧化铝上的氢气量分别为22.1 x 10(-4)和17.8 x 10(-4)molH。 g(-1)。由于在相同的条件下,H-2和D-2之间的HD交换在单独的氧化铝上并没有以明显的速率发生,因此可以得出结论,氢原子来自氧化铝的结构羟基或H2S分解产生的羟基能够从一种谷物迁移到另一种谷物并与在硫化物活性相上解离的H-2(D-2)交换。氢原子据称是通过从氧跃迁到氧化铝表面上的氧原子而作为质子迁移的,或者是被硫化氢(“穿梭分子”)输送通过气相的,硫化氢可以分解地吸附在氧化铝载体和活性相上。 D-2吸附,然后在类似条件下进行FTIR证实,在实验条件下,必须存在硫化物相才能使气相中H-2(D-2)与氢的羟基进行同位素交换可能的氧化铝。即使在暴露于D-2的5小时后,也很难在单独的硫化氧化铝上检测到OD带,而在硫化的NiMo / Al2O3上很快出现了很强的OD带。这些结果被认为有利于H-2在硫化物催化剂上的杂化裂解。 (C)1998年学术出版社。 [参考:37]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
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