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      • KCI등재

        Influence of CeO2 morphology on the catalytic oxidation of ethanol in air

        Guilin Zhou,Baoguo Gui,Hongmei Xie,Fang Yang,Yong Chen,Shengming Chen,Xuxu Zheng 한국공업화학회 2014 Journal of Industrial and Engineering Chemistry Vol.20 No.1

        Nano-CeO2 catalysts of different shapes were synthesized at different hydrothermal crystallizationtemperatures from an alkaline aqueous solution. X-ray diffraction (XRD), transmission electronmicroscope (TEM), and H2 temperature-programmed reduction (H2-TPR) were used to study thesynthesized nano-CeO2 catalyst samples. The catalytic properties of the prepared nano-CeO2 catalystsfor the catalytic oxidation of ethanol in air were also investigated. TEM analysis showed that CeO2nanorod and nanocube catalysts have been synthesized at hydrothermal crystallization temperatures of373 K and 453 K, respectively. XRD results showed that the synthesized nano-CeO2 catalysts have similarcubic fluorite structures. H2-TPR results indicated that CeO2 nanorod and nanocube catalysts exhibitdifferent reduction behaviors for H2 and that the nanorod catalyst has better low-temperature reductionperformance than the nanocube catalyst. Ethanol catalytic oxidation results indicated that oxidation andcondensation products (including acetaldehyde, acetic acid, CO2, and ethyl acetate) have been producedfrom the prepared catalysts. The ethyl acetate and acetic acid can be ignited by ethanol at lowtemperature on the CeO2(R) catalyst to give low catalytic combustion temperature for ethyl acetate andacetic acid molecules. CeO2 nanorods gave ethanol oxidation conversion rates above 99.2% at 443 K andCO2 selectivity exceeding 99.6% at 483 K, while CeO2 nanocubes gave ethanol oxidation conversion ratesof about 95.1% until 508 K and CO2 selectivity of only 93.86% at 543 K. CeO2 nanorod is a potential lowcostand effective catalyst for removing trace amounts of ethanol to purify air.

      • KCI등재

        Color center of YAlO3 with cation vacancies

        Jianyu Chen,Dunhua Cao,Guangjun Zhao,Shengming Zhou 한국물리학회 2010 Current Applied Physics Vol.10 No.2

        High quality pure YAlO3 crystal with dimension of Ø 30 × 50 ㎟ was grown by Czochralski technique. UV irradiation and air annealing bring additional absorption in the region 200–800 nm. The absorption spectra of perfect YAlO3 and YAlO3 containing cation vacancy (aluminium vacancy and yttrium vacancy)were calculated using density functional theory code CASTEP. Comparison of the simulated absorption spectra with the experimental absorption spectra of YAlO3 after UV irradiation and air annealing treatments shows that cation vacancies are responsible for part of the coloration on YAlO3 crystal.

      • KCI등재

        Catalytic combustion of volatile aromatic compounds over CuO-CeO2 catalyst

        Hongmei Xie,Qinxiang Du,Hui Li,Guilin Zhou,Shengming Chen,Zhaojie Jiao,Jianmin Ren 한국화학공학회 2017 Korean Journal of Chemical Engineering Vol.34 No.7

        Ce1−xCuxO2 oxide solid solution catalysts with different Ce/Cu mole ratios were synthesized by the one-pot complex method. The prepared Ce1−xCuxO2 catalysts were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and H2 temperature-programmed reduction (H2-TPR). Their catalytic properties were also investigated by catalytic combustion of phenyl volatile organic compounds (PVOCs: benzene, toluene, xylene, and ethylbenzene) in air. XRD analysis confirmed that the CuO species can fully dissolve into the CeO2 lattice to form CeCu oxide solid solutions. XPS and H2-TPR results indicated that the prepared Ce1−xCuxO2 catalysts contain abundant reactive oxygen species and superior reducibility. Furthermore, the physicochemical properties of the prepared Ce1−xCuxO2 catalysts are affected by the Ce/Cu mole ratio. The CeCu3 catalyst with Ce/Cu mole ratio of 3.0 contains abundant reactive oxygen species and exhibits superior catalytic combustion activity of PVOCs. Moreover, the ignitability of PVOCs is also affected by the respective physicochemical properties. The catalytic combustion conversions of ethylbenzene, xylene, toluene, and benzene are 99%, 98.9%, 94.3%, and 62.8% at 205, 220, 225, and 225 oC, respectively.

      • KCI등재

        Reduction of CO2 to CO via reverse water-gas shift reaction over CeO2 catalyst

        Bican Dai,Shiquan Cao,Hongmei Xie,Guilin Zhou,Shengming Chen 한국화학공학회 2018 Korean Journal of Chemical Engineering Vol.35 No.2

        CeO2 catalysts with different structure were prepared by hard-template (Ce-HT), complex (Ce-CA), and precipitation methods (Ce-PC), and their performance in CO2 reverse water gas shift (RWGS) reaction was investigated. The catalysts were characterized using XRD, TEM, BET, H2-TPR, and in-situ XPS. The results indicated that the structure of CeO2 catalysts was significantly affected by the preparation method. The porous structure and large specific surface area enhanced the catalytic activity of the studied CeO2 catalysts. Oxygen vacancies as active sites were formed in the CeO2 catalysts by H2 reduction at 400 oC. The Ce-HT, Ce-CA, and Ce-PC catalysts have a 100% CO selectivity and CO2 conversion at 580 oC was 15.9%, 9.3%, and 12.7%, respectively. The highest CO2 RWGS reaction catalytic activity for the Ce-HT catalyst was related to the porous structure, large specific surface area (144.9m2∙g−1) and formed abundant oxygen vacancies.

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