Selective Oxidation of Methane to Methanol over Palladium-Metallophthalocyanine Composite Catalysts at Room Temperature

被引:4
|
作者
Fan Yafang [1 ,2 ]
Wang Chunlei [1 ]
Ma Ding [1 ]
Bao Xinhe [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Liaoning, Peoples R China
[2] Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
关键词
metallophthalocyanine; palladium; gold; hydrogen peroxide; methane; selective oxidation; methanol; ZEOLITE-Y; HYDROGEN-PEROXIDE; DIRECT CONVERSION; PHTHALOCYANINE; COMPLEXES; H-2; ENCAPSULATION; PORPHYRIN; COBALT; O-2;
D O I
10.3724/SP.J.1088.2010.90833
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Iron(II), cobolt(II), and copper(II) phthalocyanines encapsulated inside the supercage of zeolite-Y were prepared by the in situ ligand synthesis method via heating the solid mixture of iron(II)-, cobolt(II)-, and copper(II)-exchanged NaY with phthalic anhydride and urea. Using hydrogen peroxide as the oxidant, the catalytic activity of these composite catalysts for methane selective oxidation was tested, and the reaction conditions were optimized. All these composite catalysts showed activity in selective oxidation of methane by hydrogen peroxide at room temperature. These composite catalysts were further loaded with Pd, Au, or PdAu, and their catalytic activity for methane oxidation with dioxygen as oxidant were examined. The coupling of encapsulated metallophthalocyanine catalysts with precious metal, which could catalyze the in situ generation of H(2)O(2), realized the activation of methane by molecular oxygen at room temperature. The results showed that the synergism between palladium and copper(II) phthalocyanine led to the improved catalytic activity in selective oxidation of methane at room temperature.
引用
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页码:302 / 306
页数:5
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