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首页> 外文期刊>Catalysis science & technology >Facile surface improvement of LaCoO3 perovskite with high activity and water resistance towards toluene oxidation: Ca substitution and citric acid etching
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Facile surface improvement of LaCoO3 perovskite with high activity and water resistance towards toluene oxidation: Ca substitution and citric acid etching

机译:肤浅表面改进LaCoO3钙钛矿活动和高耐水甲苯氧化:Ca替换和柠檬酸腐蚀

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Thermal catalytic oxidation is regarded as an effective technique to eliminate volatile organic compounds (VOCs), whereby perovskite-type oxides have been reported as low-cost and highly efficient transition metal catalysts. In this study, we employ two facile modification methods,i.e., Ca substitution and citric acid etching, to further improve the catalytic activity of LaCoO(3)perovskite for toluene oxidation. The Ca-substituted LaCoO3(La0.9Ca0.1CoO3) and citric acid-etched LaCoO3(LaCoO3-CA) showT(90)values at 220 and 215 degrees C, respectively, which are substantially lower than that of pristine LaCoO3(305 degrees C). When LaCoO(3)is modified by both Ca substitution and citric acid etching,i.e., La0.9Ca0.1CoO3-CA, theT(90)further decreases to 202 degrees C, even lower than that of the commercial catalyst 0.5 wt% Pt/Al2O3(208 degrees C). In terms of specific reaction rate at 200 degrees C, the activity of the above catalysts is also enhanced as follows: LaCoO3(0.14 mu mol s(-1)m(-2)) < La0.9Ca0.1CoO3(0.31 mu mol s(-1)m(-2)) < LaCoO3-CA (0.47 mu mol s(-1)m(-2)) < La0.9Ca0.1CoO3-CA (0.63 mu mol s(-1)m(-2)). The effects of Ca substitution and citric acid etching are discussed in light of the crystal structure, morphology, and lattice defects. On the one hand, Ca substitution and citric acid etching increase the specific surface area and pore volume, which facilitate the contact between toluene and active sites. On the other hand, these methods produce more oxygen vacancies, enhance the reducibility, and facilitate the adsorption of oxygen. The above merits result in the increase in the specific reaction rate. The modified catalysts show a better water resistance than pristine LaCoO3. As verified in the H2O-TPD characterization, this phenomenon is ascribed to the generation of surface hydroxyl groups, which are beneficial for toluene oxidation at high humidity.
机译:热催化氧化被认为是一个有效的技术来消除挥发性有机化合物(挥发性),即perovskite-type氧化物已报告是低成本和高吗有效的过渡金属催化剂。研究中,我们使用两个简单修改方法,即。蚀刻、进一步提高催化对甲苯LaCoO活动(3)钙钛矿氧化。LaCoO3 (La0.9Ca0.1CoO3)和柠檬酸acid-etchedLaCoO3 (LaCoO3-CA) showT(90)值在220年和215年度,显著的分别低于原始LaCoO3(305度C)。当LaCoO由Ca(3)修改替换和柠檬酸蚀刻,即La0.9Ca0.1CoO3-CA,提斯(90)进一步降低202摄氏度,甚至低于商业催化剂0.5 wt % Pt /氧化铝(208度C)。在特定的反应速率为200摄氏度,上述催化剂的活性加强如下:LaCoO3(0.14μ摩尔(1) (2)) < La0.9Ca0.1CoO3(0.31μ摩尔(1) (2)) < LaCoO3-CA(0.47μ摩尔年代(1)(2))< La0.9Ca0.1CoO3-CA(0.63μ摩尔年代(1)(2))。替换和柠檬酸钙的影响讨论了腐蚀的晶体结构、形态和晶格缺陷。一方面,Ca替换和柠檬酸蚀刻增加比表面积和孔隙体积,促进之间的联系甲苯和活跃的网站。这些方法产生更多的氧空位,提高还原能力和促进吸附的氧气。特定的反应速率的增加。修改后的催化剂表现出更好的抗水性比原始LaCoO3。特征,这种现象归因于表面羟基的生成,有利于甲苯氧化高吗湿度。

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