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镍、钒对FCC催化剂结构和反应性能的影响 被引量:8

Effect of Nickel and Vanadium on Structure and Catalytic Performance of FCC Catalyst
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摘要 分别通过浸渍法和循环污染法对Y型分子筛和FCC催化剂进行镍、钒污染,考察了在干燥和水热条件下镍、钒对分子筛结晶度的影响,采用高级催化裂化评价装置(ACE)评价了镍、钒污染的FCC催化剂及稀土改性FCC催化剂的催化性能。结果表明,只有在水蒸气存在条件下,钒会破坏分子筛的晶体结构;在REY分子筛中,镍的存在对分子筛结构的破坏略有影响。在FCC催化剂中,镍、钒之间存在相互作用,与单独钒污染的催化剂相比,镍、钒同时污染的催化剂的比表面积和微反活性略有提高,反应转化率由72.14%增至78.02%,重油收率由10.49%下降至7.62%。与相应的镍、钒污染FCC催化剂相比,镍、钒污染的稀土改性FCC催化剂所得转化率与总液体收率均明显增加,重油收率下降,稀土元素的引入提高了催化剂的抗镍、抗钒性能,提高了催化剂的催化性能。 Nickel(Ni)and Vanadium(V)contaminated Y zeolite and FCC catalysts were prepared by impregnation method and cyclic contamination,respectively.The effects of Ni and V on the crystallinity of zeolite in dry atmosphere and hydrothermal condition were investigated.The catalytic performance of FCC catalyst and rare earth element(RE) modified FCC catalysts contaminated by Ni and V were tested in an advanced catalytic cracking evaluation(ACE)device.Results showed that the effect of V on crystallinity of Y zeolite was evident only when steam was present.For the rare earth containing zeolite,Ni destroyed the zeolite structure slightly.A direct interaction existed between V and Ni in FCC catalyst. Compared with the FCC catalyst contaminated only by V,the FCC catalyst contaminated by both Ni and V possessed more specific surface area and slightly more MAT value,with the increase of reaction conversion from 72.14% up to 78.02%,the decrease of heavy oil yield from 10.49%to 7.62%.The conversion and total liquid yield of FCC reaction were higher,the heavy oil yield was lower over the RE modified FCC catalyst contaminated by both Ni and V than those over the Ni and V contaminated FCC catalyst,meaning that the introduction of rare earth elements in FCC catalysts enhanced the tolerance to Ni and V and cracking performance of the catalyst.
出处 《石油学报(石油加工)》 EI CAS CSCD 北大核心 2015年第5期1063-1068,共6页 Acta Petrolei Sinica(Petroleum Processing Section)
基金 "十二五"国家科技支撑计划项目(2012BAE05BO2)基金资助
关键词 催化裂化催化剂 Y型分子筛 镍钒污染 稀土 性能评价 FCC catalyst Y zeolite Ni and V contamination rare earth performance evaluation
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参考文献17

  • 1OCCELLI M L. Vanadium-zeolite interactions influidized cracking catalysts [J], Catal Rev Sci Eng,1991,33(3) : 241-280.
  • 2ALTOMARE C A,KOERMER G S, MARTINS E,et al.Vanadium interactions with treated silica aluminas [J].Appl Catal, 1988,45(2): 291-306.
  • 3MOREIRACR,HOMS N,FIERRO J L G, et al.HUSY zeolite modified by lanthanum: Effect oflanthanum introduction as a vanadium trap [ J ].Micropor Mesopor Mater, 2010,133(1-3) * 75-81.
  • 4MOREIRA C R,PEREIRA M M,ALCOBe X, et al.Nature and location of cerium in Ce-loaded Y zeolites asrevealed by HRTEM and spectroscopic techniques [J],Micropor Mesopor Mater, 2007,100(1-3) : 276-286.
  • 5ESCOBAR A S,PINTO F V,CERQUEIRA H S, et al.Role of nickel and vanadium over USY and RE-USYcoke formation[J]. Appl Catal A, 2006,315 : 68-73.
  • 6ESCOBAR A S,PEREIRA M M,CERQUEIRA H S.Effect of iron and calcium over USY coke formation[J].Appl Catal A, 2008,339(1): 61-67.
  • 7ESCOBAR A S,PEREIRA M M, PIMENTA RDM,et al. Interaction between Ni and V with USHY andrare earth HY zeolite during hydrothermal deactivation[J]. Appl Catal A,2005,286(2) : 196-201.
  • 8YANG S J, CHEN Y W,LI C. The interaction ofvanadium and nickel in USY zeolite[J]. Zeolites,1995,15: 77-82.
  • 9MOREIRA C R,HERBST M H,PISCINA P R,et al.Evidence of multi-component interaction ina V-Ce-HUSY catalyst is the cerium-EFAL interactionthe key of vanadium trapping [ J]. Micropor MesoporMater, 2008,115(3): 253-260.
  • 10张亮,田爱珍,张海涛,高雄厚,唐莉.FCC催化剂实验室循环污染老化的方法[J].石油化工,2013,42(3):276-280. 被引量:7

二级参考文献69

  • 1赵天波,萨学理,汪燮卿,陆婉珍.钒沉积对Y沸石催化剂裂化活性及物相的影响[J].石油学报(石油加工),1995,11(2):109-115. 被引量:3
  • 2苗兴东.催化裂化技术的现状及发展趋势[J].河北化工,2007,30(1):6-9. 被引量:9
  • 3宗保宁 罗一斌 等.-[J].石油学报:石油加工,1999,15(1):27-27.
  • 4陈俊武,催化裂化工艺与工程,1995年,251页
  • 5侯祥麟,中国炼油技术,1991年,127页
  • 6陈念贻,近代化学丛书.计算化学及其应用,1987年,238页
  • 7Schiavello M, et al. J. Phys. Chem. [J], 1971, 75(8): 1051-1059.
  • 8Ahari, et al. US[P], 4749572.
  • 9Inoue, et al. US[P], 4836914.
  • 10S. Y. Yang, et al. Zeolites [J], 1995, 15(1): 77.

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