催化学报
催化學報
최화학보
CHINESE JOURNAL OF CATALYSIS
2010年
4期
447-453
,共7页
宋华%于洪坤%武显春%郭云涛
宋華%于洪坤%武顯春%郭雲濤
송화%우홍곤%무현춘%곽운도
磷化二镍%二氧化钛%氧化铝%噻吩%加氢脱硫%吡啶%加氢脱氮
燐化二鎳%二氧化鈦%氧化鋁%噻吩%加氫脫硫%吡啶%加氫脫氮
린화이얼%이양화태%양화려%새분%가경탈류%필정%가경탈담
nickel phosphide%titania%alumina%thiophene%hydrodesulfurization%pyridine%hydrodenitrogenation
以溶胶-凝胶法制备的TiO_2-Al_2O_3复合氧化物为载体,采用浸渍法制备了Ni_2P/TiO_2-Al_2O_3催化剂,并用X射线衍射、N_2吸附脱附、红外和X射线光电子能谱等技术对催化剂进行了表征,考察了载体中TiO_2含量、焙烧温度及其制备方法对Ni2_P/TiO_2-Al_2O_3催化剂上同时进行噻吩加氢脱硫和吡啶加氢脱氮反应的影响.结果表明,以Ni/P摩尔比为1/2的前驱体制备的催化剂表面仅出现Ni_2P物相;当载体中TiO_2的含量为80%,焙烧温度为550℃时,Ni_2P/TiO_2-Al_2O_3催化剂上加氢脱硫和加氢脱氮的活性最高.在360℃,3.0MPa,氢/油体积比500,液时体积空速2.0h~(-1)的条件下,噻吩和吡啶转化率分别为61.3%和64.4%.
以溶膠-凝膠法製備的TiO_2-Al_2O_3複閤氧化物為載體,採用浸漬法製備瞭Ni_2P/TiO_2-Al_2O_3催化劑,併用X射線衍射、N_2吸附脫附、紅外和X射線光電子能譜等技術對催化劑進行瞭錶徵,攷察瞭載體中TiO_2含量、焙燒溫度及其製備方法對Ni2_P/TiO_2-Al_2O_3催化劑上同時進行噻吩加氫脫硫和吡啶加氫脫氮反應的影響.結果錶明,以Ni/P摩爾比為1/2的前驅體製備的催化劑錶麵僅齣現Ni_2P物相;噹載體中TiO_2的含量為80%,焙燒溫度為550℃時,Ni_2P/TiO_2-Al_2O_3催化劑上加氫脫硫和加氫脫氮的活性最高.在360℃,3.0MPa,氫/油體積比500,液時體積空速2.0h~(-1)的條件下,噻吩和吡啶轉化率分彆為61.3%和64.4%.
이용효-응효법제비적TiO_2-Al_2O_3복합양화물위재체,채용침지법제비료Ni_2P/TiO_2-Al_2O_3최화제,병용X사선연사、N_2흡부탈부、홍외화X사선광전자능보등기술대최화제진행료표정,고찰료재체중TiO_2함량、배소온도급기제비방법대Ni2_P/TiO_2-Al_2O_3최화제상동시진행새분가경탈류화필정가경탈담반응적영향.결과표명,이Ni/P마이비위1/2적전구체제비적최화제표면부출현Ni_2P물상;당재체중TiO_2적함량위80%,배소온도위550℃시,Ni_2P/TiO_2-Al_2O_3최화제상가경탈류화가경탈담적활성최고.재360℃,3.0MPa,경/유체적비500,액시체적공속2.0h~(-1)적조건하,새분화필정전화솔분별위61.3%화64.4%.
The TiO_2-Al_2O_3 complex support was prepared by the sol-gel method, and the nickel phosphide catalyst, Ni_2P/TiO_2-Al_2O_3, was made by impregnation. The catalysts were characterized by X-ray diffraction, N_2 adsorption-desorption, infrared spectroscopy, and X-ray photoelectron spectroscopy. The catalysts were evaluated on a lab-scale continuous-flow fixed-bed reactor for hydrodesulfurization (HDS) of thiophene and hydrodenitrogenation (HDN) of pyridine. The experiments were conducted to further investigate the influence of the support, i.e. the support preparation method, TiO_2 content, and support calcination temperature, on the catalyst activity. The results showed that the Ni2_P phase appeared only in the catalysts prepared from precursors with Ni/P atomic ratio of 1/2. The catalyst made from TiO_(2-)Al_2O_3 complex oxide with 80% TiO_2 as support, which was prepared by the sol-gel method and calcined at 550 ℃, exhibited the highest activity for thiophene HDS and pyridine HDN. At reaction temperature of 360 ℃, pressure of 3.0 MPa, hydrogen/oil volume ratio of 500, and liquid hourly space velocity of 2.0h~(-1), the conversion of thiophene HDS and the conversion of pyridine HDN were 61.3% and 64.4%, respectively.