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Rh-Mo-K/γ-Al_2O_3催化剂的TPR研究
引用本文:李翠华,李忠瑞.Rh-Mo-K/γ-Al_2O_3催化剂的TPR研究[J].汕头大学学报(自然科学版),1999,14(1):28-30.
作者姓名:李翠华  李忠瑞
作者单位:汕头大学科学院材料化学研究室!汕头(李翠华,施其宏),中国科学技术大学化学物理系!合肥(李忠瑞,伏义路)
摘    要:用TPR对γ-Al2O3负载的Rh催化剂和Rh-Mo-K催化剂的还原性能进行了比较研究,发现Rh催化剂在氧化过程中形成两种Rh的氧化物;向Mo-K催化剂加入铑使得Mo易还原,且Rh的氧化物部分覆盖K-Mo物种,因而形成了含有Mo-O-Rh键的混合氧化物,该物种稳定,500℃时不能被H2还原,这些氧化物提高反应活性的机理可能是降低了CO化学吸咐,增大了表面H原子的浓度,从而有利于长碳链醇的合成.

关 键 词:铑催化剂  钼基催化剂  程序升温还原

A TPR study on Rh-Mo-K/γ-Al_2O_3 catalysts
Li Cuihua, Shi Qihong.A TPR study on Rh-Mo-K/γ-Al_2O_3 catalysts[J].Journal of Shantou University(Natural Science Edition),1999,14(1):28-30.
Authors:Li Cuihua  Shi Qihong
Abstract:A comparative study is made of the reduction behaviors between aluminiasupported Rh catalysts and Rh-Mo-K catalysts with different rhodium loading by means of TPR, Oxidation of the Rh catalysts results in two forms of Rh oxide different in reduction temperature, Addition of rhodium into Mo-K system makes molybdenum easier to be reduced, and Rhodium oxides partly cover the surface of Mo-K species, thereby forming mixed oxides containing Mo-O-Rh bonds, which are so stable that they cannot be reduced by treatment with hydrogen at 500℃, A possible mechanism of these mixed oxides in the alcohol synthesis reactions is that they reduce CO chemisorption, thereby to increase the surface concentration of hydrogen atoms, thus promoting a greater increase in the synthesis of long-chain alcohols,
Keywords:rhodium catalyst  molybdenum based catalyst  temperature programming reduction (TPR)
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