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通过H2程序升温脱附实验,在H2还原的Ni/La2O3/α-Al2O3催化剂上可以明显观察到高温脱附氢(高温氢). 动力学实验结果表明,随催化剂上高温氢含量的增加, CH4/CO2重整反应的初始活性升高,同时高温氢也可在重整反应过程中原位生成,并使重整反应的活性最终达到稳定. 脉冲实验结果表明,随催化剂上高温氢含量的增加, CH4解离后生成的活性中间体CHx物种的x值也增大,进而降低了CHx与CO2反应的活化能,提高了CHx与CO2反应的速率. La2O3助剂的添加提高了Ni/La2O3/α-Al2O3催化剂上逆水气变换反应的速率,并且对CO2的活化也有促进作用. La2O3助剂的加入对于CH4/CO2重整反应的重要作用是使高温氢的数量增多且稳定性提高,有利于保持CHx物种中较高的x值,促进重整反应.

参考文献

[1] Zhang QW;Li XH;Fujimoto K .Pd-promoted Cr/ZnO catalyst for synthesis of methanol from syngas[J].Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications,2006(1):28-32.
[2] Chen Y Z;Liaw B J;Chen B J .[J].Applied Catalysis A:General,2002,236(1-2):121.
[3] Ross J R H;Van Keulen A N J;Hegarty M E S;Seshan K .[J].Catalysis Today,1996,30(1-3):193.
[4] Vannice M A .[J].Catalysis Review-Science and Engineering,1976,14(01):153.
[5] Bradford M.C.J.;Vannice M.A. .CO_2 reforming of CH_4[J].Catalysis Reviews. Science and Engineering,1999(1):1-0.
[6] Wei J M;Iglesia E .[J].Journal of Catalysis,2004,224(02):370.
[7] Batiot-Dupeyrat C.;Valderrama G.;Meneses A.;Martinez F.;Barrault J. Tatibouet JM. .Pulse study of CO2 reforming of methane over LaNiO3[J].Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications,2003(1/2):143-151.
[8] Weatherbee G D;Bartholomew C H .[J].Journal of Catalysis,1984,87(05):55.
[9] Lemonidou A A;Goula M A;Vasalos I A .[J].Catalysis Today,1998,46(2-3):175.
[10] Ashby M F;Hirth J P.Perspectives in Hydrogen in Metals[M].Oxford:Pergamon Press,1986
[11] Zeng K;Klassen T;Oelerich W;Bormann R .[J].Journal of Alloys and Compounds,1999,283(1-2):151.
[12] McLellan R B;Zang D H .[J].Journal of Physics and Chemistry of Solids,1999,60(03):347.
[13] Carr N Z;McLellan R B .[J].Acta Materialia,2004,52(11):3273.
[14] Hlil E K;Fruchart D;Miraglia S;Tobola J .[J].Journal of Alloys and Compounds,2003,356-357:169.
[15] Cui YH;Xu HY;Ge QJ;Li WZ .Kinetic study on the CH4/CO2 reforming reaction: Ni-H in Ni/alpha-Al2O3 catalysts greatly improves the initial activity[J].Journal of molecular catalysis, A. Chemical,2006(2):226-232.
[16] Kramer R;Andre M .[J].Journal of Catalysis,1979,58(02):287.
[17] Sen B;Falconer J L;Mao T F;Yu M,Flesner R L .[J].Journal of Catalysis,1990,126(02):465.
[18] Cheng Z X;Zhao X G;Li J L;Zhu Q M .[J].Applied Catalysis A:General,2001,205(1-2):31.
[19] Srivastava S;Srivastava O N .[J].Journal of Alloys and Compounds,1999,282(1-2):197.
[20] Chang J-S;Park S-E;Yoo J W;Park J-N .[J].Journal of Catalysis,2000,195(01):1.
[21] Roh H-S;Potdar H S;Jun K-W .[J].Catalysis Today,2004,93-95:39.
[22] Osaki T;Horiuchi T;Suzuki K;Mori T .[J].Journal of the Chemical Society,Faraday Transactions,1996,92(09):1627.
[23] Rostrupnielsen J R;Hansen J H B .[J].Journal of Catalysis,1993,144(01):38.
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