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    Chinese Journal of Catalysis
    2016, Vol. 37, No. 8
    Online: 29 July 2016

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    (S)-2-Aminomethylpyrrolidine-modified β-cyclodextrins were synthesized as described by Zhu and coworkers in their Article on pages 1227–1234 and used in asymmetric Michael additions of cyclohexanone and 4-nitro-β-nitrostyrene in water at room temperature. Moderate yields and higher enantioselectivity for the syn addition product were obtained.

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    Table of Contents
    Table of Contents for VOL.37 No.8
    2016, 37 (8):  0-0. 
    Abstract ( 197 )   PDF (4980KB) ( 799 )  
    Reviews
    Gas-solid catalytic reactions over ruthenium-based catalysts
    Wenbo Shi, Xiaolong Liu, Junlin Zeng, Jian Wang, Yaodong Wei, Tingyu Zhu
    2016, 37 (8):  1181-1192.  DOI: 10.1016/S1872-2067(15)61124-X
    Abstract ( 840 )   [Full Text(HTML)] () PDF (2692KB) ( 1271 )  

    Ruthenium (Ru)-based catalysts are widely employed in several types of gas-solid reactions because of their high catalytic activities. This review provides theoretical research on Ru-based catalysts and an analysis of their basic properties and oxidation behavior. There is particular emphasis on Ru-catalyzed gas-solid catalytic reactions, including the catalytic oxidation of VOCs, preferential oxidation of CO, synthesis of ammonia, oxidation of HCl and partial oxidation of CH4. Recent literature on catalysis is summarized and compared. Finally, we describe current challenges in the field and propose approaches for future development of Ru-based catalysts.

    Catalytic removal of volatile organic compounds using ordered porous transition metal oxide and supported noble metal catalysts
    Yuxi Liu, Jiguang Deng, Shaohua Xie, Zhiwei Wang, Hongxing Dai
    2016, 37 (8):  1193-1205.  DOI: 10.1016/S1872-2067(16)62457-9
    Abstract ( 647 )   [Full Text(HTML)] () PDF (3906KB) ( 1801 )  

    Most of volatile organic compounds (VOCs) are harmful to the atmosphere and human health. Catalytic combustion is an effective way to eliminate VOCs. The key issue is the availability of high performance catalysts. Many catalysts including transition metal oxides, mixed metal oxides, and supported noble metals have been developed. Among these catalysts, the porous ones attract much attention. In this review, we focus on recent advances in the synthesis of ordered mesoporous and macroporous transition metal oxides, perovskites, and supported noble metal catalysts and their catalytic oxidation of VOCs. The porous catalysts outperformed their bulk counterparts. This excellent catalytic performance was due to their high surface areas, high concentration of adsorbed oxygen species, low temperature reducibility, strong interaction between noble metal and support and highly dispersed noble metal nanoparticles and unique porous structures. Catalytic oxidation of carbon monoxide over typical catalysts was also discussed. We made conclusive remarks and proposed future work for the removal of VOCs.

    A review of the direct oxidation of methane to methanol
    Baozhai Han, Yang Yang, Yanyan Xu, U. J. Etim, Ke Qiao, Benjing Xu, Zifeng Yan
    2016, 37 (8):  1206-1215.  DOI: 10.1016/S1872-2067(15)61097-X
    Abstract ( 1153 )   [Full Text(HTML)] () PDF (729KB) ( 2622 )  

    This article briefly reviewed the advances in the process of the direct oxidation of methane to methanol (DMTM) with both heterogeneous and homogeneous oxidation. Attention was paid to the conversion of methane by the heterogeneous oxidation process with various transition metal oxides. The most widely studied catalysts are based on molybdenum and iron. For the homogeneous gas phase oxidation, several process control parameters were discussed. Reactor design has the most crucial role in determining its commercialization. Compared to the above two systems, aqueous homogenous oxidation is an efficient route to get a higher yield of methanol. However, the corrosive medium in this method and its serious environmental pollution hinder its widespread use. The key challenge to the industrial application is to find a green medium and highly efficient catalysts.

    Communications
    Direct oxidation of the Csp3-H bonds of N-heterocyclic compounds to give the corresponding ketones using a reusable heterogeneous MnOx-N@C catalyst
    Lanhui Ren, Lianyue Wang, Ying Lü, Guosong Li, Shuang Gao
    2016, 37 (8):  1216-1221.  DOI: 10.1016/S1872-2067(16)62503-2
    Abstract ( 390 )   [Full Text(HTML)] () PDF (730KB) ( 940 )  

    Novel reusable MnOx-N@C catalyst has been developed for the direct oxidation of N-heterocycles under solvent-free conditions using TBHP as benign oxidant to give the corresponding N-heterocyclic ketones. The catalytic system exhibited a broad substrate scope and excellent regioselectivity, as well as being amenable to gram-scale synthesis. This MnOx-N@C catalyst also showed good reusability and was successfully recycled six times without any significant loss of activity.

    Brönsted acid catalyzed addition of N1-p-methyl toluenesulfonyl triazole to olefins for the preparation of N2-alkyl 1,2,3-triazoles with high N2-selectivity
    Jinwei Shi, Lili Zhu, Jian Wen, Zili Chen
    2016, 37 (8):  1222-1226.  DOI: 10.1016/S1872-2067(15)61107-X
    Abstract ( 458 )   [Full Text(HTML)] () PDF (544KB) ( 816 )  

    An efficient new method has been developed to synthesize N2-alkyl 1,2,3-triazole products by toluenesulfonic acid (TsOH) catalyzed addition of N1-Ts substituted 1,2,3-triazoles to olefins. The reactions of monosubstituted and unsubstituted triazole substrates with various olefins, including vinyl esters, are explored.

    Articles
    Biomimetic asymmetric Michael addition reactions in water catalyzed by amino-containing β-cyclodextrin derivatives
    Qingying Zhu, Haimin Shen, Zhujin Yang, Hongbing Ji
    2016, 37 (8):  1227-1234.  DOI: 10.1016/S1872-2067(15)61122-6
    Abstract ( 530 )   [Full Text(HTML)] () PDF (865KB) ( 802 )  

    Nine β-cyclodextrin derivatives containing an amino group were synthesized via nucleophilic substitution from mono(6-O-p-tolylsulfonyl)-β-cyclodextrin and used in asymmetric biomimetic Michael addition reactions in water at room temperature. The mechanism responsible for the moderate activity and enantioselectivity of the β-cyclodextrin derivatives was explored using nuclear magnetic resonance spectroscopy, namely 2D 1H rotating-frame overhauser effect spectroscopy (ROESY), ultraviolet absorption spectroscopy, and quantum chemical calculations, which provide a useful technique for investigating the formation of inclusion complexes. The effects of the pH of the reaction medium, the β-cyclodextrin derivative dosage, the structure of the modifying amino group, and various substrates on the yield and enantioselectivity were investigated. The results indicated that these factors had an important effect on the enantiomeric excess (ee) in the reaction system. Experiments using a competitor for inclusion complex formation showed that a hydrophobic cavity is necessary for enantioselective Michael addition. A comparison of the reactions using 4-nitro-β-nitrostyrene and 2-nitro-β-nitrostyrene showed that steric hindrance improved the enantioselectivity. This was verified by the optimized geometries obtained from quantum chemical calculations. An ee of 71% was obtained in the asymmetric Michael addition of cyclohexanone and 2-nitro-β-nitrostyrene, using (S)-2-aminomethylpyrrolidine-modified β-CD as the catalyst, in an aqueous buffer solution, i.e., CH3COONa-HCl (pH 7.5).

    Preparation and surface characterization of nanodisk/nanoflower-structured gallium-doped zinc oxide as a catalyst for sensor applications
    R. Jothi Ramalingam, T. Radika, Hamad A. Al-Lohedan
    2016, 37 (8):  1235-1241.  DOI: 10.1016/S1872-2067(16)62464-6
    Abstract ( 374 )   [Full Text(HTML)] () PDF (3188KB) ( 1093 )  

    Nanostructured gallium-doped zinc oxide (GZO) thin films were fabricated on piezoelectric substrates. The GZO thin films with nanodisk/nanoflower morphologies were prepared by a simple spin-coating process followed by one-step hydrothermal treatment. Addition of polymer during hydrothermal treatment resulted in nanodisk and nanoflower morphologies. The morphology, microstructure and chemical composition of thin films prepared under different conditions were examined by field-emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD) and Raman spectroscopy. The XRD and FE-SEM investigations confirmed that the GZO nanodisks, nanorods and nanoflowers formed on the AlN/Si substrates were all wurtzite phase. Green fluorescent protein (GFP) was immobilized on the as-synthesized GZO nanostructured materials by a dipping process. Atomic force microscopy (AFM) and fluorescence spectroscopy measurements were conducted to confirm the surface binding nature of GFP on the GZO nanostructures to determine their suitability for use in sensor applications and bioimaging techniques. Trace-level addition of GFP to the GZO nanostructures resulted in a fluorescence response, revealing good activity for ultraviolet light sensor applications.

    Direct synthesis of nitrogen-doped mesoporous carbons for acetylene hydrochlorination
    Yong Yang, Guojun Lan, Xiaolong Wang, Ying Li
    2016, 37 (8):  1242-1248.  DOI: 10.1016/S1872-2067(16)62459-2
    Abstract ( 433 )   [Full Text(HTML)] () PDF (926KB) ( 1358 )  

    Nitrogen-doped ordered mesoporous carbon (N-OMC) catalysts were directly synthesized using SBA-15 as a hard template and sucrose as a carbon source. Urea, which was used as the nitrogen source, was carbonized with sucrose. A 3.6 wt% nitrogen doping of the carbon framework was achieved, with more than 70% of the nitrogen incorporated as quaternary nitrogen species. Only 0.2 wt% nitrogen doping, with only 32.7% quaternary nitrogen incorporation was obtained in an N-OMC catalyst (N-OMC-T) prepared using a two-step post-synthesis method. The acetylene hydrochlorination activities of N-OMC catalysts prepared via the one-step method were higher than that of the N-OMC-T catalyst because of the higher nitrogen loadings.

    Co3O4 supported on N, P-doped carbon as a bifunctional electrocatalyst for oxygen reduction and evolution reactions
    Yingbin Huang, Min Zhang, Peng Liu, Faliang Cheng, Lishi Wang
    2016, 37 (8):  1249-1256.  DOI: 10.1016/S1872-2067(16)62462-2
    Abstract ( 784 )   [Full Text(HTML)] () PDF (1400KB) ( 1484 )  

    Noble metals, such as platinum, ruthenium and iridium-group metals, are often used as oxygen reduction or evolution reaction (ORR/OER) electrocatalysts. To reduce the cost and provide an application of bifunctional catalysis, in this work, cobalt oxide supported on nitrogen and phosphorus co-doped carbon (Co3O4/NPC) was fabricated and examined as a bifunctional electrocatalyst for OER and ORR. To prepare Co3O4/NPC, NPC was pyrolyzed from melamine and phytic acid supported on carbon, followed by the solvothermal synthesis of Co3O4 on NPC. Linear sweep voltammetry was used to evaluate the activity for OER and ORR. For OER, Co3O4/NPC showed an onset potential of 0.54 V (versus the saturated calomel electrode) and a current density of 21.95 mA/cm2 at 0.80 V, which was better than both Co3O4/C and NPC. The high activity of Co3O4/NPC was attributed to a synergistic effect of the N, P co-dopants and Co3O4. For ORR, Co3O4/NPC exhibited an activity close to commercial Pt/C in terms of the diffusion limited current density (-4.49 vs -4.76 mA/cm2 at -0.80 V), and Co3O4 played the key role for the catalysis. Chronoamperometry (current versus time) was used to evaluate the stability, which showed that Co3O4/NPC maintained 46% current after the chronoamperometry test for OER and 95% current for ORR. Overall, Co3O4/NPC exhibited high activity and improved stability for both OER and ORR.

    A tetragonal tungsten bronze-type photocatalyst: Ferro-paraelectric phase transition and photocatalysis
    Dayong Fan, Ruifeng Chong, Fengtao Fan, Xiuli Wang, Can Li, Zhaochi Feng
    2016, 37 (8):  1257-1262.  DOI: 10.1016/S1872-2067(15)61126-3
    Abstract ( 340 )   [Full Text(HTML)] () PDF (537KB) ( 842 )  

    Although ferroelectrics have potential applications in photocatalysis due to their highly efficient charge separation, their mechanism of charge separation is still unknown. A ferroelectric Sr0.7Ba0.3Nb2O6 (SBN-70) semiconductor with a low ferro-paraelectric phase transition (65 ℃) was studied. The photocatalytic activity for H2 production by ferroelectric and paraelectric SBN-70 was examined. The spontaneous polarization in the ferroelectric phase strongly affected the photocatalytic performance and parallel ferroelectric domains significantly promoted photogenerated charge separation to result in better photocatalytic H2 production. This knowledge provides an important basis for the fabrication of ferroelectric photocatalysts with improved charge separation ability.

    Amine-functionalized boehmite nanoparticle-supported molybdenum and vanadium complexes: Efficient catalysts for epoxidation of alkenes
    Mahdi Mirzaee, Bahram Bahramian, Marieh Mirebrahimi
    2016, 37 (8):  1263-1274.  DOI: 10.1016/S1872-2067(16)62451-8
    Abstract ( 383 )   [Full Text(HTML)] () PDF (1472KB) ( 917 )  

    Boehmite nanoparticles with a high surface area and a high degree of surface hydroxyl groups were covalently functionalized by 3-(trimethoxysilyl)-propylamine to support vanadium-oxo-sulfate and molybdenum hexacarbonyl complexes. These supported catalysts were then characterized by Fourier-transform infrared spectroscopy, powder X-ray diffraction, thermogravimetry and differential thermal analysis, X-ray-photoelectron spectroscopy, elemental analysis, inductively coupled plasma, and transmission electron microscopy techniques. The catalysts were subsequently used for the epoxidation of cis-cyclooctene, and the experimental procedures were optimized. The progress of the reactions was investigated by gas-liquid chromatography. Recycling experiments revealed that these nanocatalysts could be repeatedly used several times for a nearly complete epoxidation of cis-cyclooctene. The optimized experimental conditions were also used successfully for the epoxidation of some other substituted alkenes.

    Preparation of nitrogen-doped carbon nanoblocks with high electrocatalytic activity for oxygen reduction reaction in alkaline solution
    Tingting Zhang, Chuansheng He, Linbo Li, Yuqing Lin
    2016, 37 (8):  1275-1282.  DOI: 10.1016/S1872-2067(15)61123-8
    Abstract ( 375 )   [Full Text(HTML)] () PDF (738KB) ( 984 )  

    The oxygen reduction reaction (ORR) is traditionally performed using noble-metals catalysts, e.g. Pt. However, these metal-based catalysts have the drawbacks of high costs, low selectivity, poor stabilities, and detrimental environmental effects. Here, we describe metal-free nitrogen-doped carbon nanoblocks (NCNBs) with high nitrogen contents (4.11%), which have good electrocatalytic properties for ORRs. This material was fabricated using a scalable, one-step process involving the pyrolysis of tris(hydroxymethyl)aminomethane (Tris) at 800 ℃. Rotating ring disk electrode measurements show that the NCNBs give a high electrocatalytic performance and have good stability in ORRs. The onset potential of the catalyst for the ORR is -0.05 V (vs Ag/AgCl), the ORR reduction peak potential is -0.20 V (vs Ag/AgCl), and the electron transfer number is 3.4. The NCNBs showed pronounced electrocatalytic activity, improved long-term stability, and better tolerance of the methanol crossover effect compared with a commercial 20 wt% Pt/C catalyst. The composition and structure of, and nitrogen species in, the NCNBs were investigated using Fourier-transform infrared spectroscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, and X-ray diffraction. The pyrolysis of Tris at high temperature increases the number of active nitrogen sites, especially pyridinic nitrogen, which creates a net positive charge on adjacent carbon atoms, and the high positive charge promotes oxygen adsorption and reduction. The results show that NCNBs prepared by pyrolysis of Tris as nitrogen and carbon sources are a promising ORR catalyst for fuel cells.

    Influence of lanthanum-doping on photocatalytic properties of BiFeO3 for phenol degradation
    Wanwan Meng, Ruisheng Hu,Jun Yang, Yanfei Du, Jingjia Li, Hongye Wang
    2016, 37 (8):  1283-1292.  DOI: 10.1016/S1872-2067(16)62449-X
    Abstract ( 479 )   [Full Text(HTML)] () PDF (1188KB) ( 1882 )  

    A series of BiFeO3 and lanthanum-doped BiFeO3 photocatalysts were synthesized by a facile sol-gel method using citric acid as complexing agent, and used to remove phenol in industrial wastewater under simulated sunlight irradiation. The samples were characterized by X-ray diffraction, energy dispersive spectroscopy, X-ray photoelectron spectroscopy, UV-Vis diffuse reflectance spectroscopy and photoluminescence spectroscopy. The introduction of La effectively suppressed the generation of an impurity phase. All the metals (La, Bi and Fe) are well distributed. Under simulated sunlight irradiation, the La-doped BiFeO3 photocatalysts exhibited superior photocatalytic activity to pure BiFeO3. The 15% La-doped BiFeO3 photocatalyst exhibited the best activity, with a degradation rate of 96% and COD removal rate of 81.53% after irradiation for 180 min, and it showed good recycling stability. The enhanced photocatalytic ability of 15% La-doped BiFeO3 was attributed to the increase of adsorbed surface hydroxyl groups, enhancement of visible light absorption and reduction of electron-hole recombination. We confirmed that the primary active species was ·OH by adding different scavengers during the photodegradation of phenol and proposed a reaction mechanism based on these experiments.

    SnO2-based solid solutions for CH4 deep oxidation: Quantifying the lattice capacity of SnO2 using an X-ray diffraction extrapolation method
    Qi Sun, Xianglan Xu, Honggen Peng, Xiuzhong Fang, Wenming Liu, Jiawei Ying, Fan Yu, Xiang Wang
    2016, 37 (8):  1293-1302.  DOI: 10.1016/S1872-2067(15)61119-6
    Abstract ( 494 )   [Full Text(HTML)] () PDF (1101KB) ( 859 )  

    A series of SnO2-based catalysts modified by Mn, Zr, Ti and Pb oxides with a Sn/M (M = Mn, Zr, Ti and Pb) molar ratio of 9/1 were prepared by a co-precipitation method and used for CH4 and CO oxidation. The Mn3+, Zr4+, Ti4+ and Pb4+ cations are incorporated into the lattice of tetragonal rutile SnO2 to form a solid solution structure. As a consequence, the surface area and thermal stability of the catalysts are improved. Moreover, the oxygen species of the modified catalysts become easier to be reduced. Therefore, the oxidation activity over the catalysts was improved, except for the one modified by Pb oxide. Manganese oxide demonstrates the best promotional effects for SnO2. Using an X-ray diffraction extrapolation method, the lattice capacity of SnO2 for Mn2O3 was 0.135 g Mn2O3/g SnO2, which indicates that to form stable solid solution, only 21% Sn4+ cations in the lattice can be maximally replaced by Mn3+. If the amount of Mn3+ cations is over the capacity, Mn2O3 will be formed, which is not favorable for the activity of the catalysts. The Sn rich samples with only Sn-Mn solid solution phase show higher activity than the ones with excess Mn2O3 species.

    Tuning of the textural features and acidic properties of sulfated mesoporous lanthana-zirconia solid acid catalysts for alkenylation of diverse aromatics to their corresponding α-arylstyrenes
    Zhongkui Zhao, Jinfeng Ran, Yongle Guo, Boyuan Miao, Guiru Wang
    2016, 37 (8):  1303-1313.  DOI: 10.1016/S1872-2067(15)61118-4
    Abstract ( 529 )   [Full Text(HTML)] () PDF (761KB) ( 837 )  

    The textural features and acidic properties of sulfated mesoporous lanthana-zirconia solid acids (SO42-/meso-La0.1Zr0.9Oδ) were efficiently tuned by modifying the conditions used to prepare the meso-La0.1Zr0.9Oδ composites, such as the molar ratio of the template to La and Zr metal ions (Nt/m), molar ratio of ammonia to La and Zr metal ions (Na/m), hydrothermal temperature (Thydro), and hydrothermal time (thydro). The effect of the textural features and acidic properties on the catalytic performance of solid acid catalysts for alkenylation of p-xylene with phenylacetylene was investigated. Various characterization techniques such as N2 physisorption, X-ray diffraction, NH3 temperature-programmed desorption, and thermogravimetric analysis were employed to reveal the relationship between the nature of catalyst and its catalytic performance. It was found that the catalytic performance significantly depended on the textural features and acidic properties, which were strongly affected by preparation conditions of the meso-La0.1Zr0.9Oδ composite. Appropriate acidic sites and high accessibility were required to obtain satisfactory catalytic reactions for this reaction. It was also found that the average crystallite size of t-ZrO2 affected by the preparation conditions had significant influence on the ultrastrong acidic sites of the catalysts. The optimized SO42-/meso-La0.1Zr0.9Oδ catalyst exhibited much superior catalytic activity and coke-resistant stability. Moreover, the developed SO42-/meso-La0.1Zr0.9Oδ catalyst demonstrated excellent catalytic performance for alkenylation of diverse aromatics with phenylacetylene to their corresponding α-arylstyrenes. Combining the previously established complete regeneration of used catalysts by a facile calcination process with the improved catalytic properties, the developed SO42-/meso-La0.1Zr0.9Oδ solid acid could be a potential catalyst for industrial production of α-arylstyrenes through clean and atom efficient solid-acid-mediated Friedel-Crafts alkenylation of diverse aromatics with phenylacetylene.

    Fe-Mn/Al2O3 catalysts for low temperature selective catalytic reduction of NO with NH3
    Xiaobo Wang, Shiguo Wu, Weixin Zou, Shuohan Yu, Keting Gui, Lin Dong
    2016, 37 (8):  1314-1323.  DOI: 10.1016/S1872-2067(15)61115-9
    Abstract ( 428 )   [Full Text(HTML)] () PDF (1905KB) ( 1062 )  

    A series of Fe-Mn/Al2O3 catalysts were prepared and studied for low temperature selective catalytic reduction (SCR) of NO with NH3 in a fixed-bed reactor. The effects of Fe and Mn on NO conversion and the deactivation of the catalysts were studied. N2 adsorption-desorption, X-ray diffraction, transmission electron microscopy, energy dispersive spectroscopy, H2 temperature-programmed reduction, NH3 temperature-programmed desorption, X-ray photoelectron spectroscopy (XPS), thermal gravimetric analysis and Fourier transform infrared spectroscopy were used to characterize the catalysts. The 8Fe-8Mn/Al2O3 catalyst gave 99% of NO conversion at 150 ℃ and more than 92.6% NO conversion was obtained in a wide low temperature range of 90-210 ℃. XPS analysis demonstrated that the Fe3+ was the main iron valence state on the catalyst surface and the addition of Mn increased the accumulation of Fe on the surface. The higher specific surface area, enhanced dispersion of amorphous Fe and Mn, improved reduction properties and surface acidity, lower binding energy, higher Mn4+/Mn3+ ratio and more adsorbed oxygen species resulted in higher NO conversion for the 8Fe-8Mn/Al2O3 catalyst. In addition, the SCR activity of the 8Fe-8Mn/Al2O3 catalyst was only slightly decreased in the presence of H2O and SO2, which indicated that the catalyst had better tolerance to H2O and SO2. The reaction temperature was crucial for the SO2 resistance of catalyst and the decrease of catalytic activity caused by SO2 was mainly due to the sulfate salts formed on the catalyst.

    Preparation of a new solid acid and its catalytic performance in di(1-naphthyl)methane hydrocracking
    Meixia Zhao, Xianyong Wei, Zhimin Zong
    2016, 37 (8):  1324-1330.  DOI: 10.1016/S1872-2067(15)61112-3
    Abstract ( 325 )   [Full Text(HTML)] () PDF (554KB) ( 811 )  

    A new solid acid was prepared by trifluoromethanesulfonic acid (TFMSA) impregnation into an acid-treated attapulgite (ATA). Di(1-naphthyl)methane (DNM) hydrocracking was used as the probe reaction to evaluate the catalytic performance of TFMSA/ATA for cleaving Car-Calk bridged bonds in coals. The results show that DNM was specifically hydrocracked to naphthalene and 1-methylnaphthalene over TFMSA/ATA in methanol in the absence of gaseous hydrogen. In particular, TFMSA/ATA was demonstrated to be stable after four cycles with slight loss in catalytic activity. Furthermore, a proposed H+ transfer mechanism successfully interprets the TFMSA/ATA-catalyzed hydrocracking reaction of DNM.

    CO oxidation over Au/ZrLa-doped CeO2 catalysts: Synergistic effect of zirconium and lanthanum
    Qi Yang, Linying Du, Xu Wang, Chunjiang Jia, Rui Si
    2016, 37 (8):  1331-1339.  DOI: 10.1016/S1872-2067(15)61113-5
    Abstract ( 518 )   [Full Text(HTML)] () PDF (1193KB) ( 900 )  

    The physicochemical properties of nanosized Au catalysts supported on doped CeO2 and their catalytic performance for the CO oxidation reaction were investigated. The Au/Zr-doped CeO2 catalyst is much more active than undoped Au/CeO2, while Au/ZrLa-doped CeO2 shows the highest activity. Characterization of the catalysts by X-ray diffraction, transmission electron microscopy (TEM), high-resolution TEM, and the X-ray absorption fine structure technique shows high homogeneity of the oxide supports and well-dispersed nanosized Au nanoparticles. Raman spectroscopy, X-ray photoelectron spectroscopy, and H2-tempeature-programmed reduction show that the surface oxygen species are the main factor for the catalytic activity in the CO oxidation reaction, while the supported Au species can improve the redox properties and create oxygen vacancy sites on the support. The oxidation state of Au is not the main factor governing the activity of Au/doped-CeO2 catalysts. Additionally, the synergistic effect of Zr and La is discussed.

    Effects of silica additive on the NH3-SCR activity and thermal stability of a V2O5/WO3-TiO2 catalyst
    Xuesong Liu, Xiaodong Wu, Tengfei Xu, Duan Weng, Zhichun Si, Rui Ran
    2016, 37 (8):  1340-1346.  DOI: 10.1016/S1872-2067(15)61109-3
    Abstract ( 499 )   [Full Text(HTML)] () PDF (551KB) ( 1159 )  

    V2O5/WO3-TiO2 and V2O5/WO3-TiO2-SiO2 catalysts were prepared by a wetness impregnation method, and both the catalysts were hydrothermally aged at 750 ℃ in 10 vol% H2O/air for 24 h. The catalysts were evaluated for NOx conversion using NH3 as the reductant. Hydrothermal ageing decreased the NOx conversion of V2O5/WO3-TiO2 catalyst severely over the entire measured temperature range. Interestingly, the NH3-SCR activity of the silica-modified catalyst at 220-480 ℃ is enhanced after ageing. The catalysts were characterized by X-ray diffraction, nitrogen adsorption, X-ray fluorescence, Raman spectroscopy, H2 temperature-programmed reduction, and NH3 temperature-programmed desorption. The addition of silica inhibited the phase transition from anatase to rutile titania, growth of TiO2 crystallite size and shrinkage of catalyst surface area. Consequently, the vanadia species remained highly dispersed and the hydrothermal stability of the V2O5/WO3-TiO2 catalyst was significantly improved.

    Ni doped La0.6Sr0.4FeO3-δ symmetrical electrode for solid oxide fuel cells
    Zhaohui Ma, Chunwen Sun, Chao Ma, Hao Wu, Zhongliang Zhan, Liquan Chen
    2016, 37 (8):  1347-1353.  DOI: 10.1016/S1872-2067(15)61116-0
    Abstract ( 398 )   [Full Text(HTML)] () PDF (2734KB) ( 1269 )  

    The conventional Ni cermet anode suffers from severe carbon deposition and sulfur poisoning when fossil fuels are used. Alternative anode materials are desired for high performance hydrocarbon fuel solid oxide fuel cells (SOFCs). We report the rational design of a very active Ni doped La0.6Sr0.4FeO3-δ (LSFN) electrode for hydrocarbon fuel SOFCs. Homogeneously dispersed Ni-Fe alloy nanoparticles were in situ extruded onto the surface of the LSFN particles during the operation of the cell. Symmetric SOFC single cells were prepared by impregnating a LSFN precursor solution onto a YSZ (yttria stabilized zirconia) monolithic cell with a subsequent heat treatment. The open circuit voltage of the LSFN symmetric cell reached 1.18 and 1.0 V in humidified C3H8 and CH4 at 750 ℃, respectively. The peak power densities of the cells were 400 and 230 mW/cm2 in humidified C3H8 and CH4, respectively. The electrode showed good stability in long term testing, which revealed LSFN has good catalytic activity for hydrocarbon fuel oxidation.

    Promotional effects of Zr on K+-poisoning resistance of CeTiOx catalyst for selective catalytic reductionof NOx with NH3
    Baoqiang Xu, Haidi Xu, Tao Lin, Yi Cao, Li Lan, Yuanshan Li, Xi Feng, Maochu Gong, Yaoqiang Chen
    2016, 37 (8):  1354-1361.  DOI: 10.1016/S1872-2067(15)61102-0
    Abstract ( 469 )   [Full Text(HTML)] () PDF (662KB) ( 1040 )  

    CeTiOx and CeZrTiOx catalysts were prepared by a coprecipitation method and used for selective catalytic reduction of NOx by NH3 (NH3-SCR). Various amounts of KNO3 were impregnated on the catalyst surface to investigate the effects of Zr addition on the K+-poisoning resistance of the CeTiOx catalyst. The NH3-SCR performance of the catalysts showed that the NOx removal activity of the Zr-modified catalyst after poisoning was better than that of the CeTiOx catalyst. Brunauer-Emmett-Teller data indicated that the Zr-containing catalyst had a larger specific surface area and pore volume both before and after K+ poisoning. X-ray diffraction, Raman spectroscopy, and transmission electron microscopy showed that Zr doping inhibited anatase TiO2 crystal grain growth, i.e., the molten salt flux effect caused by the loaded KNO3 was inhibited. The Ce 3d X-ray photoelectron spectra showed that the Ce3+/Ce4+ ratio of CeZrTiOx decreased more slowly than that of CeTiOx with increasing K+ loading, indicating that Zr addition preserved more crystal defects and oxygen vacancies; this improved the catalytic performance. The acidity was a key factor in the NH3-SCR performance; the temperature-programmed desorption of NH3 results showed that Zr doping inhibited the decrease in the surface acidity. The results suggest that Zr improved the K+-poisoning resistance of the CeTiOx catalyst.

    Efficient production of 5-hydroxymethylfurfural from hexoses using solid acid SO42-/In2O3-ATP in a biphasic system
    Yue Shen, Yuru Kang, Jiankui Sun, Chao Wang, Bo Wang, Feng Xu, Runcang Sun
    2016, 37 (8):  1362-1368.  DOI: 10.1016/S1872-2067(15)61096-8
    Abstract ( 388 )   [Full Text(HTML)] () PDF (952KB) ( 1045 )  

    A natural attapulgite (ATP)-based catalyst, sulfated In2O3-ATP (SO42-/In2O3-ATP), was obtained by an impregnation-calcination method and was used to efficiently and selectively produce the useful platform chemical 5-hydroxymethylfurfural (HMF) from hexoses. Some important reaction parameters were studied, revealing that Lewis and Brönsted acid sites on SO42-/In2O3-ATP catalyze glucose isomerization and fructose dehydration. The yields of HMF from glucose and fructose were 40.2% and 46.2%, respectively, using the optimal conditions of 180 ℃ for 60 min with 10 wt% of solid acid catalyst in a mixture of γ-valerolactone-water (9:1).

    Preparation, characterization, and catalytic performance of high efficient CeO2-MnOx-Al2O3 catalysts for NO elimination
    Xiaojiang Yao, Lulu Li, Weixin Zou, Shuohan Yu, Jibin An, Hongli Li, Fumo Yang, Lin Dong
    2016, 37 (8):  1369-1380.  DOI: 10.1016/S1872-2067(15)61098-1
    Abstract ( 595 )   [Full Text(HTML)] () PDF (1819KB) ( 1060 )  

    A series of CeO2-MnOx-Al2O3 mixed oxide catalysts (Ce:Mn:Al mole ratio = 6:4:x, x = 0.25, 0.5, 1, 2) were prepared by a simple one-step inverse co-precipitation method to investigate the influence of the incorporation of Al3+ into CeO2-MnOx mixed oxides. CeO2-MnOx, CeO2-Al2O3, and MnOx-Al2O3 mixed oxides, and CeO2 were prepared by the same method for comparison. The samples were characterized by XRD, Raman, N2 physisorption, H2-TPR, XPS, and in situ DRIFTS. The catalytic reduction of NO by CO was chosen as a model reaction to evaluate the catalytic performance. The incorporation of a small amount of Al3+ into CeO2-MnOx mixed oxides resulted in a decrease of crystallite size, with the increase of the BET specific surface area and pore volume, as well as the increase of Ce3+ and Mn4+. The former benefits good contact between catalyst and reactants, and the latter promotes the adsorption of CO and the desorption, conversion and dissociation of adsorbed NO. All these enhanced the catalytic performance for the NO+CO model reaction. A reaction mechanism was proposed to explain the excellent catalytic performance of CeO2-MnOx-Al2O3 catalysts for NO reduction by CO.

    Hydrothermal synthesis of nanosized ZSM-22 and their use in the catalytic conversion of methanol
    Lei Chen, Peng Lu, Yangyang Yuan, Li Xu, Xiaomin Zhang, Lei Xu
    2016, 37 (8):  1381-1388.  DOI: 10.1016/S1872-2067(15)61099-3
    Abstract ( 530 )   [Full Text(HTML)] () PDF (1338KB) ( 1214 )  

    ZSM-22 zeolite with different crystal lengths was prepared using a modified hydrothermal method. Rotation speed, Si/Al molar ratio and co-solvent have important effects on the crystal size of ZSM-22. The nanosized zeolite samples were characterized by X-ray diffraction, X-ray fluorescence, nitrogen adsorption, scanning electron microscopy, temperature-programmed desorption of ammonia and solid state nuclear magnetic resonance. The catalytic performance of nanosized ZSM-22 was tested using the conversion of methanol. Compared to conventional ZSM-22, the nanosized ZSM-22 zeolite exhibited superior selectivity to ethylene and aromatics and lower selectivity to propylene. Stability against deactivation was clearly shown by the nanosized ZSM-22 zeolite. A higher external surface area and smaller particle size make this nanosized ZSM-22 zeolite attractive for catalytic applications.

    Enantioselective synthesis of chiral phosphonylated 2,3-dihydrofurans by copper catalyzed asymmetric formal [3+2] cycloaddition of propargylic esters with β-keto phosphonates
    Xiushuai Chen, Chuanjin Hou, Qing Li, Yanjun Liu, Ruifeng Yang, Xiangping Hu
    2016, 37 (8):  1389-1395.  DOI: 10.1016/S1872-2067(16)62488-9
    Abstract ( 399 )   [Full Text(HTML)] () PDF (573KB) ( 850 )  

    Copper catalyzed asymmetric formal [3+2] cycloaddition of propargylic esters to β-keto phosphonates for the synthesis of chiral phosphonylated 2,3-dihydrofurans was developed. By using a bulky and structurally rigid tridentate ketimine P,N,N ligand, a series of optically active phosphonylated 2,3-dihydrofurans were prepared in high yield and up to 92% ee.

    Characterization of a novel marine microbial esterase and its use to make D-methyl lactate
    Yilong Wang, Yun Zhang, Aijun Sun, Yunfeng Hu
    2016, 37 (8):  1396-1402.  DOI: 10.1016/S1872-2067(16)62495-6
    Abstract ( 398 )   [Full Text(HTML)] () PDF (520KB) ( 830 )  

    A novel marine microbial esterase PHE14 was cloned from the genome of Pseudomonas oryzihabitans HUP022 isolated from the deep sea of the western Pacific Ocean. Esterase PHE14 exhibited very good tolerance to most organic solvents, surfactants and metal ions tested, thus making it a good esterase candidate for organic synthesis that requires an organic solvent, surfactants or metal ions. Esterase PHE14 was utilized as a biocatalyst in the asymmetric synthesis of D-methyl lactate by enzymatic kinetic resolution. D-methyl lactate is a key chiral chemical. Contrary to some previous reports, the addition of an organic solvent and surfactants in the enzymatic reaction did not have a beneficial effect on the kinetic resolution catalyzed by esterase PHE14. Our study is the first report on the preparation of the enantiomerically enriched product D-methyl lactate by enzymatic kinetic resolution. The desired enantiomerically enriched product D-methyl lactate was obtained with a high enantiomeric excess of 99% and yield of 88.7% after process optimization. The deep sea microbial esterase PHE14 is a green biocatalyst with very good potential in asymmetric synthesis in industry and can replace the traditional organic synthesis that causes pollution to the environment.

    Effect of NH4+ exchange on CuY catalyst for oxidative carbonylation of methanol
    Yuchun Wang, Huayan Zheng, Zhong Li
    2016, 37 (8):  1403-1412.  DOI: 10.1016/S1872-2067(16)62490-7
    Abstract ( 444 )   [Full Text(HTML)] () PDF (1423KB) ( 911 )  

    NaY and ion exchanged NaNH4Y zeolite with NH4NO3 were used as the support to prepare CuY catalysts by a high temperature anhydrous interaction between the support and copper (II) acetylacetonate Cu(acac)2. The catalysts were used for the oxidative carbonylation of methanol to dimethyl carbonate (DMC) at atmospheric pressure. The textural and acidic properties of NaNH4Y zeolite and the CuY catalysts were investigated by X-ray diffraction, scanning electron microscopy, N2 adsorption-desorption, temperature programmed reduction of H2, X-ray photoelectron spectroscopy and temperature programmed desorption of NH3. With increasing NH4NO3 concentration, the NH4+ exchange degree increased while the crystallinity of the zeolite remained intact. Crystalline CuO was formed when the NH4+ exchange degree of NaNH4Y was low, and the corresponding CuY catalyst showed low catalytic activity. With increasing of the NH4+ exchange degree of NaNH4Y, the content of surface bound Cu+ active centers increased and the catalytic activity of the corresponding CuY catalyst also increased. The surface bound Cu+ content reached its maximum when the NH4+ exchange degree of NaNH4Y reached towards saturation. The CuY exhibited optimal catalytic activity with 267.3 mg/(g·h) space time yield of DMC, 6.9% conversion of methanol, 68.5% selectivity of DMC.

    Changing the balance of the MTO reaction dual-cycle mechanism: Reactions over ZSM-5 with varying contact times
    Mozhi Zhang, Shutao Xu, Yingxu Wei, Jinzhe Li, Jinbang Wang, Wenna Zhang, Shushu Gao, Zhongmin Liu
    2016, 37 (8):  1413-1422.  DOI: 10.1016/S1872-2067(16)62466-X
    Abstract ( 713 )   [Full Text(HTML)] () PDF (776KB) ( 1097 )  

    The methanol to olefins (MTO) reaction was performed over ZSM-5 zeolite at 300 ℃ under various methanol weight hourly space velocity (WHSV) values. During these trials, the catalytic performance was assessed, in addition to the formation and function of organic compounds retained in the zeolite. Analysis of reaction effluents and confined organics demonstrated a dual-cycle reaction mechanism when employing ZSM-5. The extent of the hydrogen transfer reaction, a secondary reaction in the MTO process, varied as the catalyst-methanol contact time was changed. In addition, 12C/13C-methanol switch experiments indicated a relationship between the dual-cycle mechanism and the extent of the hydrogen transfer reaction. Reactions employing a low methanol WHSV in conjunction with a long contact time favored the hydrogen transfer reaction to give alkene products and promoted the generation and accumulation of retained organic species, such as aromatics and methylcyclopentadienes, which enhance the aromatic cycle. When using higher WHSV values, the reduced contact times lessened the extent of the hydrogen transfer reaction and limited the generation of methylcyclopentadienes and aromatic species. This suppressed the aromatic cycle, such that the alkene cycle became the dominant route during the MTO reaction.

    Cobalt-catalyzed redox-neutral synthesis of isoquinolines: C-H activation assisted by an oxidizing N-S bond
    Fen Wang, Qiang Wang, Ming Bao, Xingwei Li
    2016, 37 (8):  1423-1430.  DOI: 10.1016/S1872-2067(16)62491-9
    Abstract ( 578 )   [Full Text(HTML)] () PDF (580KB) ( 997 )  

    A redox-neutral avenue to access isoquinolines has been realized by a Co(III)-catalyzed C-H activation process. Starting from readily available N-sulfinyl imine substrates and alkynes, the reaction occurred via N-S cleavage with broad substrate scope and functional group compatibility in the presence of cost-effective cobalt catalysts.

    Low temperature molten salt synthesis of porous La1-xSrxMn0.8Fe0.2O3 (0 ≤ x ≤ 0.6) microspheres with high catalytic activity for CO oxidation
    Xuehui Huang, Pengju Niu, Xiaohui Shang
    2016, 37 (8):  1431-1439.  DOI: 10.1016/S1872-2067(16)62502-0
    Abstract ( 418 )   [Full Text(HTML)] () PDF (1476KB) ( 1024 )  

    A molten salt method was developed to prepare porous La1-xSrxMn0.8Fe0.2O3 (0 ≤ x ≤ 0.6) microspheres using hierarchical porous δ-MnO2 microspheres as a template in eutectic NaNO3-KNO3. X-ray diffraction patterns showed that single phase LaMn0.8Fe0.2O3 with good crystallinity was synthesized at 450 ℃ after 4 h. Transmission electron microscope images exhibited that the LaMn0.8Fe0.2O3 sample obtained at 450 ℃ after 4 h possessed a porous spherical morphology composed of aggregated nanocrystallites. Field emission scanning electron microscope images indicated that the growth of the porous LaMn0.8Fe0.2O3 microspheres has two stages. SEM pictures showed that a higher calcination temperature than 450 ℃ had an adverse effect on the formation of a porous spherical structure. The LaMn0.8Fe0.2O3 sample obtained at 450 ℃ after 4 h displayed a high BET surface area of 55.73 m2/g with a pore size of 9.38 nm. Fourier transform infrared spectra suggested that Sr2+ ions entered the A sites and induced a decrease of the binding energy between Mn and O. The CO conversion with the La1-xSrxMn0.8Fe0.2O3 (0 ≤ x ≤ 0.6) samples indicated that the La0.4Sr0.6Mn0.8Fe0.2O3 sample had the best catalytic activity and stability. Further analysis by X-ray photoelectron spectroscopy demonstrated that Sr2+ doping altered the content of Mn4+ ions, oxygen vacancies and adsorbed oxygen species on the surface, which affected the catalytic performance for CO oxidation.