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机构地区:[1]中国石油大学重质油国家重点实验室,山东东营257061 [2]中国石油长庆石化公司,陕西咸阳712000
出 处:《石油学报(石油加工)》2007年第5期33-37,共5页Acta Petrolei Sinica(Petroleum Processing Section)
基 金:山东省自然科学基金课题项目(2006ZR2203016)资助
摘 要:在渣油悬浮床加氢分散型Mo催化剂前体的硫化过程中,采用X射线光电子能谱法(XPS)分析了催化剂表面的硫化状况,并对XPS谱图进行了拟合处理。结果表明,分散型Mo催化剂前体的硫化主要形成了四配位MoS2晶体。在100℃硫化条件下,分散型Mo催化剂前体硫化产物中,Mo4+约占全部Mo物种的81.62%(摩尔分数),表面Mo活性组分硫化率为68.94%,硫化产物中有效S摩尔分数为73.06%;在300℃硫化条件下,产物中有效S摩尔分数为77.93%,表明在渣油悬浮床加氢工艺过程中,提高反应温度更有利于对分散型Mo催化剂前体的预硫化。The composition of the sulfurized products on the surface of dispersed Mo catalyst was investigated by XPS in the sulfurization of water-soluble molybdate as the precursor of the catalyst for slurry phase hydrocracking of residue. The results indicated that the sulfurized products were mainly composed of MoS2, and when the catalyst was sulfurized at 100℃, the molar fraction of Mo^4+ in total Mo species of the sulfurized catalyst was 81.62%, the sulfurization molar rate of Mo in the catalyst was 68.94%, and the molar fraction of S was 73.06%. It is also observed that the molar fraction of S was 77.93% when the sulfurization temperature was 300℃, meaning that the sulfurization of water-soluble molybdate could be carried out easier at higher temperature for slurrybed hydroprocessing of residue.
分 类 号:TE624.93[石油与天然气工程—油气加工工程]
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