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Catalyst Deactivation in Distillate Hydrotreating (Part 1) Catalyst Deactivation in the Commercial Vacuum Gas Oil Hydrotreating Unit

机译:商业真空气体油加氢处理单元中馏出水加氢处理(第1部分)催化剂去激活的催化剂去激活

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Deactivation of hydrotreating catalyst (HOP-471, Orient Catalyst) was studied in a commercial vaccum gas oil (VGO) hydrodesulfurization unit. Used catalysts were recovered from the catalyst bed at several depths in the reactor after one year of operation at 8 MPa 360-400 deg C and LHSV 2/h. The used catalysts were characterized by analysis oof carbon and the metals (V and Ni) deposited on the catalyst, by adsorption of pyrene, and by two kinds of activity test in an autoclave and a down flow reactor to compare the results obtained with those of virgin, regenerated and grained used catalysts. According to the analytical result of the used catalyst, the amount and the density of coke deposited increased with the deph of the catalyst bed (while the metal deposit decreased). Reduction in the surface area (S.A.) and pore volume (P.V.) of the catalyst with depth was not singly ascribed to the amount of coke deposited but also to its quality. The metals deposited also appeared to reduce the catalyst S.A. and P.V. The rate of of adsorption of pyrene onto the catalyst was found to increase with itd bed depth, indicating that depositions of bulky coke hinders diffusion. The catalyst at the top of the bed maintained 40% HDS activity while that at the bottom maintained 80% activity. And the regenerated catalyst at the top of the bed recovered only 20% of 60% recoverable HDS activity. However, the grained catalyst recovered 90% of HDS activity and it also recovered the normal rate of pyrene adsorption completely.
机译:研究了加氢处理催化剂(HOP-471,取向催化剂)的去激活,在商业液体油油(VGO)加氢脱硫单元中。在8MPa 360-400℃和LHSV 2 / H的一年后,在反应器中的几个深度下从催化剂床中回收二手催化剂。通过分析OOF碳和沉积在催化剂上的金属(V和Ni),通过吸附芘,并通过高压釜和下流动反应器中的两种活性试验来表征使用的催化剂,以比较与那些所获得的结果进行比较处女,再生和颗粒使用的催化剂。根据使用催化剂的分析结果,随着催化剂床的脱落(而金属沉积物减少),焦炭的量和密度增加了焦炭的量。用深度的催化剂的表面积(S.A.)和孔体积(P.V.)的孔体积(P.V.)没有单独归因于涂层的焦炭量,而且是其质量。沉积的金属也似乎减少了催化剂S.A.和P.V.发现芘在催化剂上吸附催化剂的速率随着ITD床深度而增加,表明笨重的焦炭阻碍扩散的沉积。床顶部的催化剂保持40%的HDS活性,而在底部保持80%的活性。床顶部的再生催化剂仅回收20%的可回收HDS活性的20%。然而,晶催化剂回收了90%的HDS活性,并且还完全回收了芘吸附的正常速率。

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