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    Chinese Journal of Catalysis
    2007, Vol. 28, No. 10
    Online: 25 October 2007

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    Articles
    Highly Efficient Nano-sized Fe2O3-K2O Catalyst for Dehydrogenation of Ethylbenzene to Styrene
    XIANG Bin;XU Hengyong*;LI Wenzhao
    2007, 28 (10):  841-843. 
    Abstract ( 2042 )   [Full Text(HTML)] () PDF (245KB) ( 991 )  
    A nano-sized Fe2O3-K2O catalyst was prepared by the impregnation-thermal decomposition method and was evaluated in the ethylbenzene dehydrogenation at 520-580 ℃ under normal pressure. An ethylbenzene conversion of 71.9% with a styrene selectivity of 91.1% was obtained at 550 ℃, N2/H2O/ethylbenzene molar ratio of 30.7/10/1, and WHSV of 0.43 h-1. Transmission electron microscopy andX-raydiffraction results indicated that Fe2O3 nanoparticles in the Fe2O3-K2O catalyst are well distributed with diameters of 10-14 nm. The large number of active sites in the spinel phase of the catalyst is responsible for the high catalytic activity.
    Preparation of a Cu-Ce-O Catalyst by Urea Combustion for Removing CO from Hydrogen
    HU Tao;YANG Jian;ZHAO Jun;WANG Danjun;SONG Huanling;CHOU Lingjun*
    2007, 28 (10):  844-846. 
    Abstract ( 2247 )   [Full Text(HTML)] () PDF (218KB) ( 915 )  
    A urea combustion method was employed for the preparation of the Cu-Ce-O catalyst without the need for a binder or additional calcination steps. The catalytic performance of the catalyst for preferential oxidation of CO was investigated under dry and humid feed gas conditions, and the catalyst was also examined for CO removal at the operating temperature of the PEMFC anode. A 99.3%CO conversion and 75% selectivity for CO2 could be achieved at 130 ℃ in the presence of H2O and CO2. The results of XRD and SEM characterizations indicated that copper oxides were highly dispersed on the catalyst and formed nanoparticles.
    Iridium-Catalyzed Asymmetric Hydrogenation of (2H-chromen-3-yl)methanols
    LIU Qibin;ZHOU Yonggui*
    2007, 28 (10):  847-849. 
    Abstract ( 2047 )   [Full Text(HTML)] () PDF (204KB) ( 1000 )  
    Trans-cyclohexane-backbone iridium complexes with different axial chirality were synthesized from (1R,2S)-2-(pyridin-2-yl)cyclohexanol, and their application in asymmetric hydrogenation of (2H-chromen-3-yl)methanols was investigated. When the hydrogenation was carried out using 1% Ir-8 as the catalyst at a hydrogen pressure of5 MPain dichloromethane for16 hat room temperature, excellent activities and up to 94% ee were obtained.
    Effects of Support Calcination Temperature on the Structure and Properties of NOx Storage and Reduction Catalyst K/Pt/TiO2-ZrO2
    LIU Yong;MENG Ming;GUO Lihong;ZHA Yuqing
    2007, 28 (10):  850-856. 
    Abstract ( 2244 )   [Full Text(HTML)] () PDF (500KB) ( 1046 )  
    The effects of support calcination temperature on the NOx storage capacity of the K/Pt/TiO2-ZrO2 catalyst were studied byX-raydiffraction (XRD), NH3 temperature-programmed desorption (TPD), N2 adsorption, and in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFT). The XRD results indicate that the catalyst is amorphous with support calcined at 500 ℃. With the elevation of calcination temperature to 650 ℃, ZrTiO4 crystals are formed, whose crystallization becomes more and more complete at higher temperature up to1000℃. The results of NH3-TPD reveal that the support calcined at 500 ℃ possesses the biggest amount of acidic sites; however, it decreases remarkably as the calcination temperature increases. After calcination at1000℃, the support nearly loses all the acidity. The NOx storage capacity of the samples is not proportional to the BET surface area of the supports. The sample with the support calcined at 500 ℃ shows the lowest NOx storage capacity, whereas the sample with the support calcined at 800 ℃ exhibits the highest NOx storage capacity. The results of DRIFT show that NOx is stored as NO-3 and bidentate/monodentate nitrate species in the sample with the support calcined at 500 ℃, whereas only NO-3 species is detected in other samples with the support calcined at higher temperatures. As a result, the calcination temperature influences not only the structure and acidity of the support but also the interaction between the support and the supported components. The formation of the-OKgroup arising from the interaction between the surface hydroxyl groups of support and the K-containing phases is not favorable to NOx storage, while the highly dispersed K2CO3 phase facilitates the NOx storage as nitrate.
    Synthesis and Catalytic Hydroisomerization Performance of SAPO-11 Molecular Sieve with Small Crystals
    ZHANG Shengzhen;CHEN Shengli*;DONG Peng;JI Zhiyong;Zhao Junying;Xu Keqi
    2007, 28 (10):  857-864. 
    Abstract ( 2081 )   [Full Text(HTML)] () PDF (480KB) ( 1169 )  
    On the basis of the conventional hydrothermal method, the small crystal SAPO-11 molecular sieves with sub-micron size were synthesized by controlling the aging conditions of the synthesis gel and without using other organic additives except for the template. The particles of the samples synthesized by this method possessed much smaller crystal dimension and were more uniform in size than conventionally synthesized samples. The crystal morphology of SAPO-11 samples synthesized by the improved hydrothermal method exhibited in cube shape with particle size in the range of 400-500 nm, whereas for the SAPO-11 samples synthesized by the conventional method, pseudo-spherical aggregates ranging from7 to10 μm were obtained. The sample synthesized by the improved method had larger BET surface area and larger external surface area than that of the samples prepared by the conventional hydrothermal method. The results of n-hexadecane hydroisomerization showed that the Pt/SAPO-11 catalysts synthesized by the improved method exhibited both higher catalytic activity and higher hydroisomerization selectivity than the catalysts synthesized by the conventional hydrothermal method.
    Effect of Metal-Support Interaction on Coking Resistance of Rh-Based Catalysts in CH4/CO2 Reforming
    WANG Rui;LIU Xuebin;CHEN Yanxin;LI Wenzhao;XU Hengyong*
    2007, 28 (10):  865-869. 
    Abstract ( 2135 )   [Full Text(HTML)] () PDF (251KB) ( 907 )  
    The effects of metal-support interaction on coking resistance of Rh/Al2O3, Rh/SiO2, and Rh/CeO2 catalysts during CH4/CO2 reforming were investigated. Temperature-programmed reduction and temperature-programmed oxidation (TPO) over fresh and used catalysts suggested that for Rh/Al2O3 and Rh/SiO2, the strong interaction between the metal and support led to a high dispersion of Rh after reduction. The CHx species formed on well-dispersed Rh with small Rh crystals could act as active intermediates to react with CO2 to form CO and H2. On the other hand, the carbon species formed on isolated Rh with large Rh crystals had a relatively low reactivity with CO2, which was attributed to the deactivation of catalysts. For the Rh/CeO2 catalyst, TPO and CO2 pulse experiment results indicated that the CHx species formed were more reactive than those formed on Rh/Al2O3 and Rh/SiO2. The unique Rh-CeO2 interaction resulted in the creation of CeO2-xand oxygen vacancies after partial reduction of CeO2, which facilitated the CO2 dissociation. As a result, the dissociated surface oxygen could readily react with CHx species, thereby inhibiting the carbon deposition over Rh/CeO2.
    Non-Pt Anode Catalysts for Alkaline Direct Alcohol Fuel Cells
    CHEN Yougui;ZHUANG Lin*;LU Juntao
    2007, 28 (10):  870-874. 
    Abstract ( 1969 )   [Full Text(HTML)] () PDF (388KB) ( 1649 )  
    Pd- and Au-based binary catalysts have been tested as non-Pt anode catalysts for alkaline direct alcohol fuel cells toward the electrooxidation of methanol, ethanol, and ethylene glycol. The activity of Pd for alcohol oxidation is very low in acid but relatively high in alkaline, in which an onset potential can be observed around0.4 V(vs RHE). After incorporation of Ru, the onset potential shifts negatively ca 0.15 V. It is notable that Pd-Ru is extremely active for ethanol oxidation, and the current density is four times that on Pt-Ru within 0.3-0.4 V. Whereas Au is inert in acid for the electrooxidation of alcohol, but it is somewhat active in alkaline. An anodic current of alcohol oxidation can be observed in alkaline at potentials positive than0.6 V(vs RHE). Au-Ru exhibits higher activity than Au at relatively positive potentials, but it does not cause a negative shift in the onset potential, which may imply that the dissociative adsorption of alcohol molecules on the Au surface is the rate-determining step at relatively negative potentials.
    Preparation and Catalytic Performance of Gold Nanoparticles Stabilized by Thioether-Functionalized Ionic Liquid
    LI Biaomo;YU Ningya*;WANG Pingjun;JIN Yong;YIN Donghong;*
    2007, 28 (10):  875-879. 
    Abstract ( 2171 )   [Full Text(HTML)] () PDF (306KB) ( 1327 )  
    A novel thioether-functionalized ionic liquid (TFIL) was synthesized and applied as a stabilizer for the preparation of gold nanoparticles (GNP) in the ionic liquid of 1-n-butyl-3-methylimidazolium hexafluorophosphate. GNP stabilized by TFIL (GNP-TFIL) were characterized by Fourier transform infrared spectroscopy, ultraviolet-visible spectroscopy, and transmission electron microscopy. GNP-TFIL remained the structure of TFIL after GNP was stabilized by TFIL. GNP-TFIL displayed an interface resonance absorption appearing around 526 nm, which suggests the formation of GNP. GNP stabilized by TFIL could be dispersed uniformly with the particle size of2.0-3.6nm. GNP exhibited high catalytic activity in the epoxidation of styrene and could be reused. The conversion of styrene and the selectivity for styrene oxide were as high as 100% and 88.5%, respectively, when the reaction was performed at 45 ℃ for6 husing 3-chloroperoxybenzoic acid as the oxidant.
    Activation of Carbon Dioxide by Electrocatalysis for Synthesis of Ethyl Carbanilate
    NIU Dongfang;XU Chengtian;ZHANG Li;LUO Yiwen;ZHANG Kai;LU Jiaxing*
    2007, 28 (10):  880-884. 
    Abstract ( 2262 )   [Full Text(HTML)] () PDF (245KB) ( 1386 )  
    CO2 was elctrochemically activated by the Ni(bpy)3Cl2 catalyst and reacted with aniline and iodoethane to ethyl carbanilate under mild conditions (p(CO2)=0.1 MPa, 20 ℃). The CO2 activation mechanism and the synthesis reaction mechanism were proposed. The electroreductive potential of CO2 was moved from-2.1V to-1.6V owing to the Ni(bpy)3Cl2 catalyst in DMF solution, indicating that the reaction condition was effectively improved. The catalyst showed a good effect on the CO2 activation, and the selectivity for ethyl carbanilate was 100%. The effects of the catalyst, the electrolytic potentials, the nature of the working electrode, the temperature, the supporting electrolytes, and the passed charge amount per mole of aniline supplied to the electrode on the yield of ethyl carbanilate were studied. Under the optimized electrolytic conditions, the maximal yield of ethyl carbanilate was 60.8%.
    La3+Modification of ZnO-TiO2 Coupled Semiconductors and Their Photocatalytic Activity
    CHENG Gang;*;ZHOU Xiaode;LI Yan;TONG Panrui;WANG Liming
    2007, 28 (10):  885-889. 
    Abstract ( 2334 )   [Full Text(HTML)] () PDF (336KB) ( 1024 )  
    Modification of nanocrystalline coupled semiconductor ZnO-TiO2 by means of La3+doping using the sol-gel method was investigated. Thermogravimetry-differential scanning calorimetry, scanning electron microscopy,X-raydiffraction, and Raman spectroscopy were employed to analyse the structure and morphology of La3+/ZnO-TiO2. The degradation of reactive red K-2BP was used to evaluate the photocatalytic activity of the catalyst under UV-lamp (253.7 nm, 20 W) irradiation. Effects of La3+doping concentration and calcination temperature on photocatalytic activity were investigated at a fixed photocatalyst amount and air flow rate. The results showed that La3+doping caused an increase in crystal transformation temperature, a strong blue shift of diffraction peaks, and a decrease in grain size. The reactive red K-2BP could be fully degraded within 40 min when La3+doping content was 0.5% and calcination temperature was 500 ℃. Under these conditions, the apparent absorption coefficient reached 0.182 min-1, which was 1.4 times as large as coupled semiconductor ZnO-TiO2.
    Preparation of Alumina Nanoparticles by Supercritical Antisolvent Process
    HE Chunyan;JIANG Haoxi*;ZHANG Minhua
    2007, 28 (10):  890-894. 
    Abstract ( 2224 )   [Full Text(HTML)] () PDF (453KB) ( 1095 )  
    The supercritical antisolvent (SAS) process is a novel technique for micronization and has a promising prospect in the production of thermosensitive explosives, polymer microspheres, medicines, superconductors, catalysts, and dyestuffs. Using carbon dioxide as the antisolvent medium and anhydrous ethanol as the solvent, nanoparticles of the aluminum nitrate precursor were prepared by the SAS process. The effects of preparation conditions including precipitation temperature and solution concentration on the SAS process were investigated. Spherical nanoparticles of alumina were prepared through calcination of the aluminum nitrate precursor. The nanoparticles were characterized by thermogravity-mass spectroscopy,X-raydiffraction, transmission electron microscopy, and field emission gun transmission electron microscopy. The reduction properties of nickel supported by SAS alumina nanoparticles were studied by temperature-programmed reduction. It is found that alumina nanoparticles show better dispersion properties for the active component nickel than the commercialγ-Al2O3sample.
    Synthesis of TS-1 Using Inorganic SiO2-TiO2 Precursor and Its Catalytic Performance for Hydroxylation of Phenol
    ZHANG Haijiao;YAO Mingkai;XIE Wei;LIU Yueming*;WU Peng
    2007, 28 (10):  895-899. 
    Abstract ( 2328 )   [Full Text(HTML)] () PDF (369KB) ( 837 )  
    An inorganic SiO2-TiO2 precursor havingSi-O-Tibonds similar to those present in titaniumsilicate molecular sieve was prepared through spontaneous dispersion of Ti(SO4)2 on amorphous porous silica by thermal treatment. A TS-1 molecular sieve was then synthesized successfully using the inorganic SiO2-TiO2 precursor by hydrothermal crystallization templated by tetrapropylammonium hydroxide. Characterization usingX-raydiffraction, Fourier transform infrared spectroscopy, and ultraviolet-visible absorption spectroscopy showed that a higher proportion of titanium species in the precursor withSi-O-Tibonds was incorporated into the TS-1 framework during the crystallization process, while the titanium species as a bulk TiO2 phase remained unchanged. Conditions affecting the catalytic performance of TS-1 were investigated in detail. The results indicated that the proper conditions were that the treatment temperature for precursor was about 450 ℃, the molar ratio of silica to titanium was 40, the crystallization temperature was about 160-170 ℃, and the crystallization time was about 48-72 h. TS-1 prepared under the above conditions showed that the activity for hydroxylation of phenol was comparable to TS-1 made by the classical method.
    Improvement of Dynamic Respondence of a Proton Exchange Membrane Fuel Cell over a Polyaniline-Modified Pt/C Catalyst
    GAN Quanquan;XU Hongfeng*;ZHANG Maofeng
    2007, 28 (10):  900-904. 
    Abstract ( 2091 )   [Full Text(HTML)] () PDF (393KB) ( 1009 )  
    A proton exchange membrane fuel cell (PEMFC) possesses several advantages such as high energy density, low operating temperature, and fast startup, which make PEMFC the most promising and attractive candidate for electric vehicles and portable power. However, operations of fuel cells in the application of these systems are dynamic, and the transient behavior happens when the load changes. Transient operations may result in the oxidant starvation due to gas response rate lagging the loading rate, which will affect the durability and reliability of fuel cells further. In this paper, polyaniline (PANI) as a supercapacitor material was hybridized with a PEMFC catalyst in the electrode in order to buffer the load. PANI was synthesized by the chemical method using sulfide acid as the dopant. The PANI-Pt/C catalyst was prepared by mixing PANI and Pt/C in ultrasound and drying in air. The cyclic voltammetry of 10%PANI-Pt/C demonstrates that PANI can effectively improve oxygen reduction rate. The fuel cell performance is also improved by PANI according to the single fuel cell polarization experiment. The dynamic respondence of voltage to current and the multi-potential step chronoamperometry show that PANI can buffer and stabilize the voltage during the transient current loading and working at a large current.
    Photocatalytic Performance and Doping Mechanism of B-S Co-doped TiO2
    WEI Fengyu*;NI Liangsuo
    2007, 28 (10):  905-909. 
    Abstract ( 2313 )   [Full Text(HTML)] () PDF (321KB) ( 1161 )  
    A B-S-co-doped TiO2 photocatalyst (TiO2-B-S) was prepared by the hydrothermal method.X-raydiffraction, ultraviolet-visible diffuse reflectance spectroscopy, andX-rayphotoelectron spectroscopy were applied to characterize the crystalline structure, light absorbing ability, and the chemical state of boron and sulfur in the photocatalysts. The results of photocatalytic degradation of methyl orange demonstrated that the TiO2-B-S catalyst prepared at 240 ℃ for12 hexhibited the highest photocatalytic activity, and the degradation ratio of methyl orange were 99.8% and 81% under UV light irradiation for 50 min and sunlight irradiation for 230 min, respectively. The characterization results revealed that TiO2-B-S is in conformity with the anatase TiO2, and the doping of boron and sulfur ions could efficiently inhibit the grain growth. Doped boron was present as the form of B3+in B-doped TiO2 samples, forming a possible chemical environment likeTi-O-B. The higher UV-visible light photocatalytic activity of co-doped TiO2 was attributed to the doped boron, which lowered the band gap and resulted in a localized crystal deformation. The doping of B and S enhanced the surface acidity and visible light absorption ability of TiO2. Photocatalytic activity of TiO2-B-S was enhanced due to the synergistic effect of B and S.
    Surface Modification of MCM-41 Molecular Sieve and Its Catalytic Performance for Synthesis of Iso-amyl Acetate
    CHEN Jing;HAN Mei;LI Guiyun;WANG Jintang*
    2007, 28 (10):  910-914. 
    Abstract ( 2127 )   [Full Text(HTML)] () PDF (332KB) ( 1052 )  
    MCM-41 molecular sieve was synthesized by the sol-gel method and functionalized with benzyl sulphonic acid and trimethylchlorosilane using a post-synthetic procedure. The organic groups were covalently bonded to the surface of MCM-41 by etherification ofSi-OHand thus a new S-B-MCM-41 catalyst was prepared. The structure and Brnsted acid amount of S-B-MCM-41 catalyst were characterized by XRD, N2 adsorption-desorption, and acid-base titration. The results showed that the mesoporous structure of MCM-41 was maintained in the S-B-MCM-41 catalyst with a BET surface area of 798 m2/g and acid capacity of 4.0 mmol/g. The synthesis of iso-amyl acetate from acetic acid and iso-amyl alcohol over S-B-MCM-41 catalyst and its catalytic performance were investigated. Under the optimum conditions of acetic acid 0.1 mol, iso-amyl alcohol 0.15 mol, catalyst0.2 g, water-entrainer toluene 15 ml, reaction temperature 110-125 ℃, and reaction time2 h, the esterification fraction was over 99%. By comparison, the MCM-41 molecular sieve only had an esterification fraction of 54% under the same conditions. After three times of repeated use, the esterification fraction above 90% still maintained over S-B-MCM-41. The reaction mechanism for the esterification was discussed.
    Epoxidation of Cyclohexene Catalyzed by the Vanadium Bromoperoxidase from Corallina officinalis
    YU Yao;JIN Yan;WU Peichun;ZHANG Wei*
    2007, 28 (10):  915-918. 
    Abstract ( 2095 )   [Full Text(HTML)] () PDF (241KB) ( 1296 )  
    The epoxidation of cyclohexene catalyzed by a vanadium bromoperoxidase from the red algae Corallina officinalis has been investigated. The reaction was performed in a water-organic solvent biphasic system. The effects of oxidants and their loading method, pH, temperature, and the concentration of vanadium bromoperoxidase and KBr on the epoxidation were studied. The optimal conditions were as follows: the reaction temperature was 55 ℃, and 50 μl of 2.29 mol/L H2O2 was added every 10 min to the Tris-HCl buffer at pH 6.0 containing 50 mmol/L of KBr and 32 U/ml of the enzyme (final concentration). Under these conditions, the maximum epoxy cyclohexane yield and selectivity were 41.5% and 82.2%, respectively.
    Catalytic Performance of Several Zeolite Catalysts for Oligomerization of Butene-2
    LIU Shu;;WANG Ligang;LIU Hongchao;SUN Xinde;LIU Zhongmin*
    2007, 28 (10):  919-924. 
    Abstract ( 2042 )   [Full Text(HTML)] () PDF (316KB) ( 875 )  
    Butene-2 oligomerization was performed in a continuous flow fixed-bed reactor. Several zeolite catalysts with different acidity and textural properties were investigated in order to show the effects of acidity and pore size on the catalyst activity and selectivity for butene-2 oligomerization. A solid phosphorous acid catalyst was included as comparison. The acidity and pore size of various zeolites are important factors that influence the catalyst activity and selectivity for higher olefins in oligomerization. The zeolite with an 8-membered ring system shows low activity because of the strong diffusion resistance to butene-2. The zeolite with an 12-membered ring system lessens the diffusion limitation and results in a higher activity at lower temperature. As for the zeolites with a 10-membered ring system, the pore size and strong acidity improve the catalyst activity and selectivity for higher olefins further. Compared with the solid phosphorous acid catalyst with C=9+selectivity of less than 30%, the zeolite catalysts, such as ZSM-5, ZSM-22, and β with 10- and 12-membered ring systems and with strong acid sites, show C=9+selectivity of more than 50%, which indicates the better catalytic performance of the zeolite catalysts.
    Effect of Silica Promoter on Iron-Based Catalyst for Fischer-Tropsch Synthesis
    WANG Weijia;LI Jinlin*;LUO Mingsheng
    2007, 28 (10):  925-930. 
    Abstract ( 2096 )   [Full Text(HTML)] () PDF (794KB) ( 1003 )  
    A series of SiO2-incorporated precipitated Fe-Si-Cu-K (100Fe∶xSi∶3.0Cu∶2.0K, x=0, 2.8, 6.4, 8.2, atomic ratio) catalysts were prepared using the co-precipitation method for the Fischer-Tropsch synthesis (FTS). The in-situX-raydiffraction (XRD) and N2 physisorption were used to characterize the catalysts. The catalytic properties for FTS were tested in a fixed-bed reactor under pressure of 1.0 MPa and temperature of 543 K. The SiO2 incorporation increased the surface area and decreased the pore size of the precipitated iron catalysts, and the transition of different iron oxide and iron carbide phases (Fe2O3, Fe3O4, Fe3C, Fe5C2, and Fe7C3) was detected by in-situ XRD during the catalyst reduction in CO and FTS reaction in syngas (H2/CO molar ratio=0.7). The activity of the catalyst without SiO2 increased sharply with time on stream during the FTS process, which was accompanied by the transition of Fe5C2 to Fe7C3. The catalyst without SiO2 deactivated rapidly when the highest CO conversion was achieved, whereas a persistent increase in the activity of catalysts with SiO2 was achieved with time on stream. These indicate that SiO2 can stabilize the activity of the precipitated iron catalyst. The observed effects of SiO2 on the catalytic performance of precipitated iron catalysts can be explained by the fact that SiO2 can improve the dispersity of iron oxides and iron carbides in the catalyst and restrain the conversion of different iron carbide phases during the catalyst reduction and FTS reaction.