首页> 外文期刊>The Korean journal of chemical engineering >An experimental and kinetic study of toluene oxidation over LaMn1-x B (x) O-3 and La(0.8)A(0.2)Mn(0.3)B(0.7)O(3) (A=Sr, Ce and B=Cu, Fe) nano-perovskite catalysts
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An experimental and kinetic study of toluene oxidation over LaMn1-x B (x) O-3 and La(0.8)A(0.2)Mn(0.3)B(0.7)O(3) (A=Sr, Ce and B=Cu, Fe) nano-perovskite catalysts

机译:LaMn1-x B(x)O-3和La(0.8)A(0.2)Mn(0.3)B(0.7)O(3)上甲苯氧化的实验和动力学研究(A = Sr,Ce和B = Cu ,Fe)纳米钙钛矿催化剂

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摘要

Catalytic oxidation of toluene over perovskite-type oxides of the general formula LaMn1-xBxO3 (B=Cu, Fe and x=0, 0.3, 0.7) and La(0.8)A(0.2)Mn(0.3)B(0.7)O(3) (A=Sr, Ce and B=Cu, Fe) was investigated, where the catalysts were synthesized by sol-gel auto combustion method. The catalysts were characterized by XRD, BET, H-2-TPR, XPS, and SEM. Obtained XRD patterns confirmed the perovskites to be single-phase perovskite-type oxides. Specific surface areas of perovskites were obtained between 25-40m(2)/g. The perovskite catalysts showed high activity for the toluene oxidation. Based on the results, Fe-containing perovskite catalysts exhibited higher activity than Cu-containing perovskite catalysts. The substitution of Sr and Ce in A-site of the perovskite catalysts enhanced their activity for toluene oxidation. Among different synthesized catalysts in this research, La0.8Ce0.2Mn0.3Fe0.7O3 has the highest activity. Nearly complete elimination of toluene was achieved at 200 A degrees C with this catalyst. Based on Langmuir-Hinshelwood mechanisms, kinetic studies were conducted on toluene oxidation, indicating LH-OS-ND (adsorption of reagents on same types of sites and non-dissociative adsorption of oxygen) as the most probable mechanism which could predict the experimental data with correlation coefficient of R-2=0.9952.
机译:通式为LaMn1-xBxO3(B = Cu,Fe和x = 0,0.3,0.7)和La(0.8)A(0.2)Mn(0.3)B(0.7)O()的钙钛矿型氧化物上的甲苯催化氧化3)研究了(A = Sr,Ce和B = Cu,Fe),其中通过溶胶-凝胶自动燃烧法合成催化剂。通过XRD,BET,H-2-TPR,XPS和SEM对催化剂进行了表征。获得的XRD图谱证实钙钛矿为单相钙钛矿型氧化物。钙钛矿的比表面积在25-40m(2)/ g之间。钙钛矿催化剂显示出对甲苯氧化的高活性。基于该结果,含Fe的钙钛矿催化剂显示出比含Cu的钙钛矿催化剂更高的活性。在钙钛矿型催化剂的A-位取代Sr和Ce增强了它们对甲苯氧化的活性。在这项研究的不同合成催化剂中,La0.8Ce0.2Mn0.3Fe0.7O3具有最高的活性。用该催化剂在200℃下几乎完全消除了甲苯。基于Langmuir-Hinshelwood机理,对甲苯氧化进行了动力学研究,表明LH-OS-ND(相同类型位点上的试剂吸附和氧的非解离吸附)是最有可能预测实验数据的机理。 R-2的相关系数= 0.9952。

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