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首页> 外文期刊>Journal of Catalysis >GAMMA-ALUMINA-SUPPORTED PT CATALYSTS FOR AROMATICS REDUCTION - A STRUCTURAL INVESTIGATION OF SULFUR POISONING CATALYST DEACTIVATION
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GAMMA-ALUMINA-SUPPORTED PT CATALYSTS FOR AROMATICS REDUCTION - A STRUCTURAL INVESTIGATION OF SULFUR POISONING CATALYST DEACTIVATION

机译:γ-氧化铝支持的芳香族还原PT催化剂-硫中毒催化剂失活的结构研究

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The effects of sulfur poisoning on the structural changes of gamma-alumina-supported Pt catalysts were investigated by X-ray absorption spectroscopy and temperature-programmed reduction (TPR). Extended X-ray absorption fine structure (EXAFS) analysis of the fresh catalyst determined an average Pt-Pt coordination number of 2.6, suggesting an average platinum cluster size of 3 and 4 atoms formed on the gamma-alumina surface. After the test reaction using a tetralin feed containing 1000 ppm sulfur at 270 degrees C and 32 atm for 24 h, an increase of Pt cluster size was observed. A concomitant increase of the Pt-Pt coordination number to 7.3 with the formation of Pt-S contribution in EXAFS indicate that metal migration was induced by sulfur poisoning. The Pt-S contributions with bond distance of 2.34 and 2.53 Angstrom were obtained by subtracting the Pt-Pt contribution from Fourier-isolated raw data. The results, combined with TPR peaks characterizing the sulfur-poisoned catalysts, suggest that the two Pt-S contributions were due to the interaction between Pt and the adsorbed H2S and the formation of platinum sulfide (PtS). After the fresh catalysts were tested with more severe operation conditions (19 atm, 2000 ppm sulfur), the used catalysts were characterized by only one Pt-S contribution of bond distance 2.31 Angstrom, indicating that clusters with a morphology closely resembling bulk PtS were formed on the surface. Based on the structural investigation results, we conclude that the loss of catalyst activity during sulfur poisoning is attributed to the adsorption of H2S, sulfur-poisoning-induced Pt agglomeration and the formation of PtS. (C) 1997 Academic Press. [References: 36]
机译:通过X射线吸收光谱和程序升温还原(TPR)研究了硫中毒对γ-氧化铝负载的Pt催化剂结构变化的影响。新鲜催化剂的扩展X射线吸收精细结构(EXAFS)分析确定平均Pt-Pt配位数为2.6,表明在γ-氧化铝表面上形成的平均铂簇尺寸为3和4个原子。使用含有1000 ppm硫的四氢化萘进料在270摄氏度和32个大气压下进行测试反应24小时后,观察到Pt簇尺寸增加。随着EXAFS中Pt-S贡献的形成,Pt-Pt配位数随之增加至7.3,表明金属迁移是由硫中毒引起的。通过从傅立叶分离的原始数据中减去Pt-Pt贡献,可以得到键距为2.34和2.53埃的Pt-S贡献。结果与表征硫中毒催化剂的TPR峰相结合,表明这两种Pt-S贡献是由于Pt与吸附的H2S之间的相互作用以及硫化铂(PtS)的形成。在更严格的操作条件(19 atm,2000 ppm硫)下对新鲜催化剂进行测试后,所用催化剂的特征在于键距仅为2.31埃的一种Pt-S贡献,表明形成了形态与本体PtS非常相似的簇在表面上。根据结构研究结果,我们得出结论,硫中毒期间催化剂活性的损失归因于H2S的吸附,硫中毒引起的Pt团聚和PtS的形成。 (C)1997学术出版社。 [参考:36]

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