首页> 外文期刊>Journal of the Japan Petroleum Institute >Formation of Rh2P Supported on Na-form Zeolites and Catalytic Activity for Hydrodesulfurization
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Formation of Rh2P Supported on Na-form Zeolites and Catalytic Activity for Hydrodesulfurization

机译:Na型沸石负载的Rh2P的形成及加氢脱硫的催化活性

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摘要

The effects of zeolite structure on rhodium phosphide (Rh2P) formation, dispersion and hydrodesulfurization (HDS) activity were investigated. TPR showed that the order of maximum peak temperature for phosphates reduction was Na-beta>NaMFI>NaMOR. The XRD patterns of reduced catalysts revealed that the order of Rh2P formation temperature agreed with that of phosphate reducibility. CO uptake of NaMOR-supported catalyst was much lower than those of other zeolite-supported catalysts. These results suggested that since the NaMOR support had a one-dimensional channel, the phosphates and Rh species did not easily diffuse into the micropores. The order of thiophene HDS conversion was NaMFI>Na-beta NaMOR. The order of average particle size of Rh2P calculated from TEM images was NaMOR>Na-beta approximate to NaMFI. Since formation of Rh2P on the Na-beta needed high reduction temperature, the beta structure might be partially collapsed. Well-dispersed Rh2P was formed on NaMFI at lower reduction temperature, so that this catalyst exhibited the highest HDS activity among the zeolite-supported catalysts.
机译:研究了沸石结构对磷化铑(Rh2P)的形成,分散和加氢脱硫(HDS)活性的影响。 TPR表明,磷酸盐还原的最高峰值温度顺序为Na-β> NaMFI> NaMOR。还原催化剂的XRD图谱表明,Rh2P形成温度的顺序与磷酸盐还原性的顺序一致。 NaMOR负载的催化剂的CO吸收量远低于其他沸石负载的催化剂。这些结果表明,由于NaMOR载体具有一维通道,因此磷酸盐和Rh种类不容易扩散到微孔中。噻吩HDS的转化顺序为NaMFI>Na-β NaMOR。由TEM图像计算的Rh2P的平均粒径的顺序为NaMOR>Na-β,近似于NaMFI。由于在Na-beta上形成Rh2P需要较高的还原温度,因此beta结构可能会部分塌陷。在较低的还原温度下,NaMFI上形成了分散良好的Rh2P,因此该催化剂在沸石负载的催化剂中具有最高的HDS活性。

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