首页> 外文期刊>Catalysis Today >Highly active MoS2,CoMoS2 and NiMoS2 unsupported catalysts prepared by hydrothermal synthesis for hydrodesulfurization of 4,6-dimethyldibenzothiophene
【24h】

Highly active MoS2,CoMoS2 and NiMoS2 unsupported catalysts prepared by hydrothermal synthesis for hydrodesulfurization of 4,6-dimethyldibenzothiophene

机译:通过水热合成制备高活性MoS2,CoMoS2和NiMoS2无载体催化剂,用于4,6-二甲基二苯并噻吩的加氢脱硫

获取原文
获取原文并翻译 | 示例
           

摘要

This paper reports on a comparative study of unsupported MoS2 and Me/MoS2(Me = Co,Ni)catalysts prepared by hydrothermal synthesis in our laboratory.Hydrothermal synthesis using water and organic solvent under hydrogen was found to produce highly active Mo based sulfide nano-size particles.MoS2 had high surface area(320 m~2/g)and large pore volume(0.72 m~3/g).Addition of Co or Ni promoter decreased surface area and pore volume.Compared to MoS2,downward shifts of the reduction temperatures were observed in TPR for Co(Ni)-Mo-S sulfides which suggested a decrease in metal sulfur bond strength.HRTEM and XRD results showed that MoS2 formed large crystallized particles but the particle growth was inhibited when promoters were incorporated.For HDS,4,6-dimethyldibenzothiophene(4,6-DMDBT)was slightly more reactive than dibenzothiophene(DBT)over the MoS2.The liquid-phase adsorption showed that 4,6-DMDBT had higher capacity and stronger interaction with the adsorption site on MoS2 than DBT.In distinct contrast to MoS2,the promoted NiMo or CoMo sulfide showed higher liquid-phase adsorption selectivity for DBT than for 4,6-DMDBT.The promoter increased activity of MoS2 and changed the contribution of the direct-desulf urization and of hydrogenation pathways.The adsorption and HDS results indicated that promoter affects both the number and the activity of active sites of the Mo sulfides.HDS activity of the unsupported Mo based sulfides was much higher than that of the sulfided commercial Co(Ni)Mo/Al2O3 catalysts.
机译:本文报道了在我们实验室中通过水热合成制备的无载体MoS2和Me / MoS2(Me = Co,Ni)催化剂的比较研究。发现水和有机溶剂在氢气下进行水热合成可以生产出高活性的Mo基硫化物纳米颗粒。 MoS2具有较高的表面积(320 m〜2 / g)和较大的孔体积(0.72 m〜3 / g)。添加Co或Ni促进剂会降低表面积和孔体积。与MoS2相比,MoS2的向下移动Co(Ni)-Mo-S硫化物的TPR降低了温度,这表明金属硫键的强度降低了.HRTEM和XRD结果表明MoS2形成了大的结晶颗粒,但掺入促进剂时却抑制了颗粒的生长。 4,4,6-二甲基二苯并噻吩(4,6-DMDBT)在二硫化钼上的反应活性高于二苯并噻吩(DBT)。液相吸附表明4,6-DMDBT具有更高的容量和与MoS2上吸附位点的相互作用。比DBT.In dist与MoS2相比,促进的NiMo或CoMo硫化物对DBT的液相吸附选择性高于对4,6-DMDBT的吸附。促进剂增加了MoS2的活性并改变了直接脱硫和氢化途径的作用。吸附和HDS结果表明助催化剂同时影响Mo硫化物的活性位点和活性。未负载的Mo基硫化物的HDS活性远高于硫化Co(Ni)Mo / Al2O3商用催化剂。

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