石油化工高等学校学报
石油化工高等學校學報
석유화공고등학교학보
JOURNAL OF PETROCHEMICAL UNIVERSITIES
2014年
4期
27-30,56
,共5页
镍基催化剂%石油树脂%加氢
鎳基催化劑%石油樹脂%加氫
얼기최화제%석유수지%가경
Ni-based catalyst%Petroleum resin%Hydrotreating
采用共沉淀法制备镍基催化剂的前躯物,该前躯物经捏合成型焙烧后制成石油树脂加氢催化剂。对沉淀工艺条件、助剂及不同镍盐进行考察。结果表明,通过调整沉淀工艺条件参数,可以制备出适合石油树脂加氢所需的大孔催化剂;选择合适的镍盐和助剂,能够制备出镍晶粒较小的镍基催化剂,同时助剂的加入抑制了 Ni 晶粒的增长并提高催化剂容硫能力。制备的镍基石油树脂催化剂具有很强的烯烃饱和性能,且加氢后石油树脂的软化点下降幅度很小。加氢前后的石油树脂结构变化很小,说明所制备的催化剂具有很强的烯烃饱和性能,且加氢后石油树脂的软化点下降幅度很小。
採用共沉澱法製備鎳基催化劑的前軀物,該前軀物經捏閤成型焙燒後製成石油樹脂加氫催化劑。對沉澱工藝條件、助劑及不同鎳鹽進行攷察。結果錶明,通過調整沉澱工藝條件參數,可以製備齣適閤石油樹脂加氫所需的大孔催化劑;選擇閤適的鎳鹽和助劑,能夠製備齣鎳晶粒較小的鎳基催化劑,同時助劑的加入抑製瞭 Ni 晶粒的增長併提高催化劑容硫能力。製備的鎳基石油樹脂催化劑具有很彊的烯烴飽和性能,且加氫後石油樹脂的軟化點下降幅度很小。加氫前後的石油樹脂結構變化很小,說明所製備的催化劑具有很彊的烯烴飽和性能,且加氫後石油樹脂的軟化點下降幅度很小。
채용공침정법제비얼기최화제적전구물,해전구물경날합성형배소후제성석유수지가경최화제。대침정공예조건、조제급불동얼염진행고찰。결과표명,통과조정침정공예조건삼수,가이제비출괄합석유수지가경소수적대공최화제;선택합괄적얼염화조제,능구제비출얼정립교소적얼기최화제,동시조제적가입억제료 Ni 정립적증장병제고최화제용류능력。제비적얼기석유수지최화제구유흔강적희경포화성능,차가경후석유수지적연화점하강폭도흔소。가경전후적석유수지결구변화흔소,설명소제비적최화제구유흔강적희경포화성능,차가경후석유수지적연화점하강폭도흔소。
The precursors of Ni-based petroleum resin hydrogenation catalyst were prepared by coprecipitation and were made into hydrogenation catalyst through a series of process.The coprecipitation conditions,promoters and different nickel salts were studied in detail.The results showed that the large pore catalysts of petroleum resin hydrogenation was prepared by adjusting coprecipitation process parameters.The Ni-based catalysts of small Ni grain was prepared by selecting the suitable nickel salt and promoter,and the promoter can inhibit Ni grain to grow up and improve the catalyst capacity of holding sulfur. The Ni-based petroleum resin hydrogenation catalyst was provided with very strong olefin saturation properties,and its softening point of hydrogenated petroleum resin had a less decrease.