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Hydroisomerization of n-dodecane on a new kind of bifunctional catalyst: Nickel phosphide supported on SAPO-11 molecular sieve

机译:新型双功能催化剂上正十二烷的加氢异构化:SAPO-11分子筛上负载的磷化镍

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摘要

A new type of nickel phosphide catalysts supported on SAPO-11 was used for the hydroisomerization of n-dodecane. Their properties were characterized by means of N2-sorption, H2-TPR, XRD, XPS, DRIFTS of adsorbed pyridine, CO chemisorption, and NH3-TPD and H2-TPD. The effects of the Ni/P ratio and the nickel content on catalyst performance were investigated. For comparison, the property and performance of Ni/SAPO-11 were also considered. Compared to Ni/SAPO-11, SAPO-11 supported nickel phosphides had higher isomerization selectivity due to their lower hydrogenolysis activity. As the Ni/P ratio deceased, the n-dodecane conversion decreased, while the isododecane selectivity reached its maximum at the Ni/P ratio of 1. As the nickel content increased, the n-dodecane conversion and isododecane selectivity reached their maximum. In short, a balance between medium strength acid sites and Ni sites was required for obtaining high n-dodecane conversion and isododecane selectivity. Moreover, there was a synergism between the Ni sites and the medium strength acid site. Under suitable conditions, the isododecane yield reached about 65% on Ni2P/SAPO-l 1 containing 3 wt% Ni.
机译:SAPO-11上负载的新型磷化镍催化剂用于正十二烷的加氢异构化。通过N2-吸附,H2-TPR,XRD,XPS,吸附吡啶的DRIFTS,CO化学吸附以及NH3-TPD和H2-TPD表征了它们的性质。研究了Ni / P比和镍含量对催化剂性能的影响。为了进行比较,还考虑了Ni / SAPO-11的性质和性能。与Ni / SAPO-11相比,SAPO-11负载的磷化镍因其较低的氢解活性而具有较高的异构化选择性。随着Ni / P比的降低,正十二烷转化率降低,而异十二烷选择性在Ni / P比为1时达到最大值。随着镍含量的增加,正十二烷转化率和异十二烷选择性达到最大值。简而言之,为了获得高正十二烷转化率和异十二烷选择性,需要在中等强度的酸位点和Ni位点之间取得平衡。此外,在Ni位点和中等强度的酸位点之间存在协同作用。在合适的条件下,在含有3重量%的Ni的Ni 2 P / SAPO-1 1上,异十二烷的产率达到约65%。

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