当代化工
噹代化工
당대화공
CONTEMPORARY CHEMICAL INDUSTRY
2015年
5期
922-925
,共4页
刘君君%丁巍%王鼎聪%郭胜辉
劉君君%丁巍%王鼎聰%郭勝輝
류군군%정외%왕정총%곽성휘
活性金属量%硅溶胶%改性%低堆积密度
活性金屬量%硅溶膠%改性%低堆積密度
활성금속량%규용효%개성%저퇴적밀도
Amount of active metal%Silica sol%Modification%Low bulk density
提出通过硅改性来增加催化剂活性金属负载量的一种方法,采用压汞法和 N2吸附法对硅改性后的三次纳米自组装 Mo-Ni/γ-Al2O3催化材料的孔性质进行表征。压汞法数据表明,催化材料的孔容为0.66~0.90 cm3?g-1,比表面积为122~175 m2?g-1,30~100 nm 的孔径分布高达69.08%。结果表明,加硅后催化剂金属上量增加,单位体积活性金属量降低以及堆积密度降低,而且其催化效果在200 h 后趋于稳定,具有脱硫、加氢脱残碳效果好等优点。
提齣通過硅改性來增加催化劑活性金屬負載量的一種方法,採用壓汞法和 N2吸附法對硅改性後的三次納米自組裝 Mo-Ni/γ-Al2O3催化材料的孔性質進行錶徵。壓汞法數據錶明,催化材料的孔容為0.66~0.90 cm3?g-1,比錶麵積為122~175 m2?g-1,30~100 nm 的孔徑分佈高達69.08%。結果錶明,加硅後催化劑金屬上量增加,單位體積活性金屬量降低以及堆積密度降低,而且其催化效果在200 h 後趨于穩定,具有脫硫、加氫脫殘碳效果好等優點。
제출통과규개성래증가최화제활성금속부재량적일충방법,채용압홍법화 N2흡부법대규개성후적삼차납미자조장 Mo-Ni/γ-Al2O3최화재료적공성질진행표정。압홍법수거표명,최화재료적공용위0.66~0.90 cm3?g-1,비표면적위122~175 m2?g-1,30~100 nm 적공경분포고체69.08%。결과표명,가규후최화제금속상량증가,단위체적활성금속량강저이급퇴적밀도강저,이차기최화효과재200 h 후추우은정,구유탈류、가경탈잔탄효과호등우점。
A new method was put forward to increase the amount of loading active metal by the silicon modification. The pore properties of silicon modified third nano self-assembly macroporous Mo-Ni/γ-Al2O3 catalytic materials were characterized by mercury porosimetry and N2 adsorption method. It is shown that the catalytic materials have pore volume of 0.66~0.90 cm3?g-1, specific surface area of 122~175 m2?g-1, and the pore size distribution reaches up to 69.08% at the range of 30~100 nm by the mercury porosimetry. The results show that the amount of loading active metal are increased, the amount of unit volume active metal and the bulk density are decreased by the silicon modification;The catalytic performance of hydrodesulfurization and hydrodecarbonresidue is better when the hydrogenation reaction tends to stable after 200 h.