摘要
In the current study simultaneous reactions of hydrodesulfurization(HDS) of dibenzothiophene(DBT) and reforming of methanol in a micro-autoclave reactor were studied over bi-metallic(Co-Mo/Al2O3 and Ni-Mo/Al2O3) and tri-metallic(Pd-Co-Mo/Al2O3 and Pd-Ni-Mo/Al2O3) catalyst systems which were prepared by incipient impregnation method.In situ hydrogen utilization and low Pd loadings were the major targets of this study.For comparison purpose,catalytic activity was separately determined for both the methanol reforming and HDS of DBT reactions as well.Ni based catalysts were confirmed with better activity than Co ones for both the reactions with Pd promoted ones ranking at the top i.e.Pd-Ni-Mo/Al2O3 > Ni-Mo/Al2O3 > Pd-Co-Mo/Al2O3 > Co-Mo/Al2O3 where Pd-Ni-Mo/Al2O3 showed 91% DBT conversion at 380 ℃ and 12 h reaction time.Some of the selected organic additives on catalytic activity were tested for their effect toward HDS reaction which was unique with close relation to their chemical nature.Reaction products were quantitatively and qualitatively analyzed via HPLC and GC-MS techniques respectively which helped in elucidating reaction mechanism.
In the current study simultaneous reactions of hydrodesulfurization (HDS) of dibenzothiophene (DBT) and reforming of methanol in a micro-autoclave reactor were studied over bi-metallic ( Co-Mo/Al2O3 and Ni-Mo/Al2O3 ) and tri-metallic ( Pd-Co- Mo/Al2O3 and Pd-Ni-Mo/Al2O3 ) catalyst systems which were prepared by incipient impregnation method. In situ hydrogen utilization and low Pd loadings were the major targets of this study. For comparison purpose, catalytic activity was separately determined for both the methanol reforming and HDS of DBT reactions as well. Ni based catalysts were confirmed with better activity than Co ones for both the reactions with Pd promoted ones ranking at the top i.e. Pd-Ni-Mo/Al2O3 〉 Ni-Mo/Al2O3 〉 Pd- Co-Mo/Al2O3 〉 Co-Mo/Al2O3 where Pd-Ni-Mo/A12 03 showed 91% DBT conversion at 380 ℃ and 12 h reaction time. Some of the selected organic additives on catalytic activity were tested for their effect toward HDS reaction which was unique with close relation to their chemical nature. Reaction products were quantitatively and qualitatively analyzed via HPLC and GC-MS techniques respectively which helped in elucidating reaction mechanism.
出处
《燃料化学学报》
EI
CAS
CSCD
北大核心
2012年第6期714-720,共7页
Journal of Fuel Chemistry and Technology
基金
Fundamental Research Foundation of Sinopec(X505015)
关键词
加氢脱硫
二苯并噻吩
催化剂
高效液相色谱法
in situ hydrodesulfurization of DBT
methanol reforming
Pd promoted alumina based catalyst
organic additive