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    Chinese Journal of Catalysis
    2013, Vol. 34, No. 10
    Online: 29 September 2013

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    Gao and coworkers in their Communication on pages 1811–1815 reported the application of perovskite hollow nanospheres for the catalytic wet air oxidation (CWAO) of lignin. As the substrate, lignin is degraded to monomers such as vanillin and oligomers. These products are highly value-added. Meanwhile, the catalysts show both high catalytic activity and excellent stability.

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    Table of Contents for Vol. 34 No. 10
    2013, 34 (10):  0-0. 
    Abstract ( 186 )   PDF (1517KB) ( 771 )  
    Reviews
    Theoretical and practical discussion of measurement accuracy for physisorption with micro- and mesoporous materials
    Zheling Zhang, Zhenghong Yang
    2013, 34 (10):  1797-1810.  DOI: 10.1016/S1872-2067(12)60691-9
    Abstract ( 643 )   [Full Text(HTML)] () PDF (674KB) ( 964 )  

    The surface area and pore size distribution are two very basic properties of a solid catalyst powder. Physisorption is still the only macroscopic method for measuring these two properties. To better understand the pore structure and surface properties of materials, it is very important to make accurate physisorption measurements. Unfortunately there are still many misunderstandings about physisorption. In fact, hardware design, operation of the instrument and data reduction can all contribute to the accuracy of a measurement. In this paper, the measurement accuracy of physisorption was discussed from these three aspects.

    Communications
    Perovskite hollow nanospheres for the catalytic wet air oxidation of lignin
    Peng Gao, Changzhi Li, Hua Wang, Xiaodong Wang, Aiqin Wang
    2013, 34 (10):  1811-1815.  DOI: 10.1016/S1872-2067(12)60691-3
    Abstract ( 332 )   [Full Text(HTML)] () PDF (565KB) ( 599 )  

    A urea-assisted solvothermal-calcination method was used to prepare LaFexMn1-xO3 and La0.9Sr0.1MnO3 hollow nanospheres, and their crystal phase, morphology, and specific surface area properties were analyzed by X-ray diffraction, transmission electron microscopy, and nitrogen adsorption-desorption isotherms. These materials were then evaluated as catalysts for the catalytic wet air oxidation (CWAO) of lignin, and showed much better catalytic performance than perovskite prepared by the traditional sol-gel method. The structure of the hollow nanospheres has been suggested as the reason of this higher catalytic activity. For the CWAO reaction at 120 ℃ and 0.2 MPa O2, the conversion of lignin was greater than 80% after 1 h. Analysis of the ions leaching from the material following the completion of the reaction showed that the catalysts were very stable under the reaction conditions because of their perovskite phase structure.

    Ru(Ⅱ)-catalyzed ring expansion of alkynylcyclopropanes in the presence of sulfonamides
    Yuye Chen, Junsong Wang, Xingwei Li, Aiqun Jia
    2013, 34 (10):  1816-1819.  DOI: 10.1016/S1872-2067(12)60680-9
    Abstract ( 264 )   [Full Text(HTML)] () PDF (342KB) ( 630 )  

    Ru(II)-catalyzed ring expansion of alkynylcyclopropanes to alkylidenecyclobutanamines using a variety of cyclopropane and sulfonamide substrates was developed and shown to give moderate to excellent yields.

    Articles
    Adsorbed CO induced change of the adsorption site and charge of Au adatoms on FeO(111)/Ru(0001)
    Runhai Ouyang, Wei-Xue Li
    2013, 34 (10):  1820-1825.  DOI: 10.1016/S1872-2067(12)60664-0
    Abstract ( 384 )   [Full Text(HTML)] () PDF (466KB) ( 677 )  

    A first principles study of the influence of CO adsorption on the charge state, adsorption site, and stability of Au adatoms on FeO/Ru(0001) was presented. Calculations were first carried out to explore the detailed interface structure of a bilayer FeO(111) film on Ru(0001). The HCP domain inside the Moire supercell has a rather small rumpling with both the Fe and O atoms directly bonded to the Ru substrate. The most stable adsorption of an Au atom on FeO/Ru(0001) is at the Fe-bridge site in the HCP domain, where Au binds with two flipped Fe atoms and is negatively charged. After exposure to CO, the Au anions at the Fe-bridge site changed their position to the O-top site by overcoming a small barrier of only 0.12 eV, where they formed stable Au+-CO species with a significant reduction in the formation energy. The results highlighted the importance of in situ characterization of supported catalysts under reaction conditions, and implications on catalyst stability were also discussed.

    Effects of pretreatment on performance and structure of Ni-Co bimetallic catalyst for biogas reforming to hydrogen
    Jian Zhao, Wei Zhou, Jianxin Ma
    2013, 34 (10):  1826-1832.  DOI: 10.1016/S1872-2067(12)60648-2
    Abstract ( 288 )   [Full Text(HTML)] () PDF (1335KB) ( 665 )  

    Ni-Co bimetallic catalysts supported on g-Al2O3 pellets for biogas reforming to hydrogen were successfully prepared using the excessive impregnation method. The effects of pretreatment on the catalytic performance were investigated in a fixed-bed vertical quartz reactor under conditions of 850 ℃, 0.1 MPa, and a gas hourly space velocity of 6000 mL gcat-1 h-1 (4 g of catalyst, 2.5-3.5 mm). The samples were characterized using X-ray diffraction, transmission electron microscopy, thermogravimetry coupled to differential scanning calorimetry, and emission scanning electron microscopy with energy-dispersive X-ray spectroscopy. The results showed that the catalyst pretreated with both H2 and CO2 showed higher activity, and basically eliminated the long induction period of the biogas reforming reaction, compared with the catalyst pretreated with only H2. In a 511 h stability test, the catalyst pretreated with both H2 and CO2 exhibited excellent stability, with a very low carbon deposition rate, ca. 0.2 mg gcat-1 h-1. The average conversion of CH4 and CO2, selectivity for H2 and CO, and ratio of H2/CO were 96%, 97%, 98%, 99%, and 0.98, respectively. The characterization results showed that the catalyst pretreated with both H2 and CO2 exhibited higher carbon formation resistance and better anti-sintering performance during reactions; this resulted in smaller metal particles and thus enhanced the stability of the catalyst. This new pretreatment route is very promising for enhancing the performance of biogas reforming catalysts.

    Effect of supports on the structure and activity of vanadium-chromium oxide catalysts for ammoxidation of 3-picoline
    Feng Jiang, Shengcai Deng, Lei Niu, Guomin Xiao
    2013, 34 (10):  1833-1838.  DOI: 10.1016/S1872-2067(12)60650-0
    Abstract ( 307 )   [Full Text(HTML)] () PDF (493KB) ( 494 )  

    Bulk and Nb2O5-, MgF2-, TiO2-, and SiO2-supported vanadium-chromium oxide catalysts were prepared by the incipient wetness impregnation method and investigated for the ammoxidation of 3-picoline to nicotinonitrile at 310-400 ℃. The physical and chemical properties of the catalysts were assessed by X-ray diffraction, N2 adsorption-desorption, H2-temperature-programmed reduction, and NH3-temperature-programmed desorption. The surface area of the supports influenced the formation of the active components of the catalysts: high surface area encouraged the formation of monoclinic CrVO4 whereas low surface area favored the formation of orthorhombic CrVO4. The high reducibility of vanadium in the catalyst and the large number of surface active sites resulted in higher 3-picoline conversion efficiencies. The high selectivity was attributed to the low surface acidity of the catalysts. Reaction temperature showed a positive effect on the catalytic performance for it could increase 3-picoline conversion and maintain nicotinonitrile selectivity.

    Desulfurization of liquid fuels using air-assisted performic acid oxidation and emulsion catalyst
    Ahmad Imtiaz, Ahmad Waqas, Ishaq Muhammad
    2013, 34 (10):  1839-1847.  DOI: 10.1016/S1872-2067(12)6668-8
    Abstract ( 393 )   [Full Text(HTML)] () PDF (805KB) ( 860 )  

    Catalytic oxidative desulfurization (ODS) of model oil and commercial oil samples was investigated using an air-assisted performic acid oxidation system with a phase transfer or emulsion catalyst comprising a quaternary ammonium salt-based heteropolyoxometalate. Different emulsion catalysts with a Keggin type heteroployoxometalate anion (containing W, Mo, and V) and cetyltrimethylammonium bromide cation were prepared and characterized by X-ray fluorescence, Fourier transform infrared spectroscopy, and scanning electron microscopy. [C16H33N(CH3)3]3[PW9Mo3O40] was the most effective catalyst in the current oxidation system, which reduced the sulfur content of the model oil from 1275 μg/g to 57 μg/g. The reactivity order of different model sulfur compounds was thiophene < dibenzothiophene < 4,6-dimethyldibenzothiophene. The ODS of model sulfur compounds followed first order kinetics with apparent activation energy from 29 to 27 kJ/mol. The catalysts also performed efficiently in the ODS of the industrial oil samples, including untreated naphtha, light gas oil, heavy gas oil, and Athabasca oil sands derived bitumen, for which sulfur removal rates were 83%, 85%, 68% and 64%, respectively.

    Silica gel-supported TEMPO with adsorbed NOx for selective oxidation of alcohols under mild conditions
    Hua Zhang, Luoling Fu, Hongmin Zhong
    2013, 34 (10):  1848-1854.  DOI: 10.1016/S1872-2067(12)60657-3
    Abstract ( 356 )   [Full Text(HTML)] () PDF (472KB) ( 708 )  

    A column padding silica gel was used to support 2,2,6,6-tetramethylpiperdine-1-oxyl (TEMPO) and to adsorb NOx to provide an oxidant system for the selective oxidation of alcohols. A wide range of alcohols were oxidized to the corresponding aldehydes and ketones with high selectivities and conversions using this heterogeneous catalyst under mild conditions.

    First-principle insights into the catalytic role of indium oxide in methanol steam reforming
    Sen Lin, Xinxin Ye
    2013, 34 (10):  1855-1860.  DOI: 10.1016/S1872-2067(12)60662-7
    Abstract ( 347 )   [Full Text(HTML)] () PDF (679KB) ( 726 )  

    Using first-principle methods, we have shown that formaldehyde can be selectively converted to CO2 over In2O3(110). The OH generated from the splitting of water was found to assist in the dehydrogenation of formaldehyde to give the corresponding formyl (CHO) species. Rather than direct dehydrogenation, a hydrogen atom from the CHO was then removed by a neighboring OH to produce CO. Finally, in favoring of desorption, the CO seized a lattice O atom to yield CO2. Our calculation results indicate that In2O3 plays an important role in terms of selectivity during the methanol steam reforming reaction without the participation of the PdIn alloy, confirming the experimentally observed selectivity towards CO2.

    Poly(4-vinylpyridinium butane sulfonic acid) hydrogen sulfate: An efficient, heterogeneous poly(ionic liquid), solid acid catalyst for the one-pot preparation of 1-amidoalkyl-2-naphthols and substituted quinolines under solvent-free conditions
    Ali Reza Kiasat, Arash Mouradzadegun, Seyyed Jafar Saghanezhad
    2013, 34 (10):  1861-1868.  DOI: 10.1016/S1872-2067(12)60659-7
    Abstract ( 349 )   [Full Text(HTML)] () PDF (852KB) ( 715 )  

    Poly(4-vinylpyridinium butane sulfonic acid) hydrogen sulfate has been used as an efficient dual acidic catalyst for the one-pot preparation of 1-amidoalkyl-2-naphthols and substituted quinolines under solvent-free conditions. The catalyst was characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, and thermo-gravimetric analysis. The results revealed several advantages to our new catalyst system, including its reusability, facile work-up procedure, eco-friendly reaction conditions, short reaction time, and high product yields.

    Nanostructure-based electrochemical sensor for the voltammetric determination of benserazide, uric acid, and folic acid
    Sakineh Esfandiari Baghbamidi, Hadi Beitollahi, Seyed Zia Mohammadi, Somayeh Tajik, Somayeh Soltani-Nejad, Vahhab Soltani-Nejad
    2013, 34 (10):  1869-1875.  DOI: 10.1016/S1872-2067(12)60655-X
    Abstract ( 338 )   [Full Text(HTML)] () PDF (374KB) ( 608 )  

    A carbon paste electrode modified with carbon nanotubes and ferrocene was fabricated. An electrochemical study of the modified electrode and an investigation into its efficiency for the electrocatalytic oxidation of benserazide, uric acid and folic acid were undertaken. The electrode was also used to study the electrocatalytic oxidation of benserazide using cyclic voltammetry, chronoamperometry, and square wave voltammetry (SWV). We found that the oxidation of benserazide at the surface of the modified electrode occurs at a potential about 285 mV lower than that of unmodified carbon paste electrode. SWV gave a linear dynamic range from 8.0×10-7 to 7.0×10-4 mol/L. The detection limit was 1.0×10-7 mol/L for benserazide. This modified electrode was used for the determination of benserazide, uric acid, and folic acid in an urine sample.

    Visible-light photocatalytic efficiencies and anti-photocorrosion behavior of CdS/graphene nanocomposites:Evaluation using methylene blue degradation
    Jiajia Yan, Kun Wang, Hui Xu, Jing Qian, Wei Liu, Xingwang Yang, Huaming Li
    2013, 34 (10):  1876-1882.  DOI: 10.1016/S1872-2067(12)60677-9
    Abstract ( 596 )   [Full Text(HTML)] () PDF (553KB) ( 1005 )  

    A series of CdS nanocrystals/graphene (CdS/GR) nanocomposites with various graphene contents were prepared. Their photocatalytic efficiencies and anti-photocorrosion behavior were studied using methylene blue degradation under visible-light irradiation. The results showed that the introduction of graphene improved the migration efficiency of photogenerated carriers and inhibited charge carrier recombination. The photocatalytic efficiencies of the as-prepared CdS/GR nanocomposites were influenced by the graphene content, achieving a maximum at a graphene content of 4.6 wt% (denoted by CdS/GR-4.6%). The anti-photocorrosion behavior of the CdS/GR-4.6% nanocomposite was further investigated using a photoelectrochemical method and X-ray diffraction analysis. The photocorrosion of CdS nanocrystals was effectively suppressed after the introduction of graphene sheets. Compared with bare CdS nanocrystals, the photocurrent of the CdS/GR-4.6% nanocomposites increased 2.3-fold.

    Multiwall carbon nanotube paste electrode with 3,4-dihydroxy-cinnamic acid as mediator for the determination of glutathione in pharmaceutical and urine samples
    Mohsen Keyvanfard, Hassan Karimi-Maleh, Khadijeh Alizad
    2013, 34 (10):  1883-1889.  DOI: 10.1016/S1872-2067(12)60661-5
    Abstract ( 262 )   [Full Text(HTML)] () PDF (686KB) ( 658 )  

    A sensitive and selective electrochemical sensor for the determination of glutathione (GSH) was developed using a modified multiwall carbon nanotube paste electrode with 3,4-dihydroxy-cinnamic acid as a mediator. This modified electrode showed very high electrocatalytic activity for the anodic oxidation of GSH. Under the optimized conditions, the electrocatalytic peak current showed a linear relationship with GSH concentration in the range of 0.5-400.0 μmol/L with a detection limit of 0.1 μmol/L GSH. The relative standard deviations for seven successive assays of 5.0 and 25.0 μmol/L GSH were 2.2% and 2.7%, respectively. The modified electrode was used for the determination of GSH compounds in real urine samples.

    Succinimide-N-sulfonic acid catalyzed synthesis of bis(indolyl)methane and coumarin derivatives under mild conditions
    Farhad Shirini, Nader Ghaffari Khaligh
    2013, 34 (10):  1890-1896.  DOI: 10.1016/S1872-2067(12)60669-X
    Abstract ( 305 )   [Full Text(HTML)] () PDF (307KB) ( 833 )  

    A mild and simple procedure is described for the synthesis of bis(indolyl)methane and coumarin derivatives using succinimide-N-sulfonic acid as an efficient, cheap, and reusable catalyst under mild conditions.

    Papain enzyme supported on magnetic nanoparticles:Preparation, characterization and application in the fruit juice clarification
    Leila Mosafa, Majid Moghadam, Mohammad Shahedi
    2013, 34 (10):  1897-1904.  DOI: 10.1016/S1872-2067(12)60663-9
    Abstract ( 405 )   [Full Text(HTML)] () PDF (446KB) ( 1161 )  

    The preparation, characterization, and application of silica-coated magnetic nanoparticles for papain immobilization is reported. Papain was covalently attached onto the (3-chloropropyl) trimethoxysilane-modified silica-coated magnetic nanoparticles. The enzyme-immobilized nanoparticles were characterized by Fourier transform infrared spectroscopy, X-ray powder diffraction, scanning electron microscopy, and vibrating sample magnetometry techniques. Response surface methodology combined with statistical analyses using Minitab were employed to evaluate optimum operating conditions to immobilize papain on the magnetic nanoparticles. The optimum conditions were: temperature = 27.3 ℃, pH of the enzyme solution = 7.1, concentration of papain = 3.3 mg/mL, and immobilization time = 10 h. Compared with the free papain, the immobilized papain displayed enhanced enzyme activity, better tolerance to variations in the medium pH and temperature, improved storage stability, and good reusability. Both the free and immobilized enzymes were effective for the clarification of pomegranate juice.

    Precursors of active Ni species in Ni/Al2O3 catalysts for oxidative dehydrogenation of ethane
    Lucie Smoláková, Šárka Botková, Libor Čapek, Peter Priecel, Agnieszka Sołtysek, Martin Kout, Lenka Matějová
    2013, 34 (10):  1905-1913.  DOI: 10.1016/S1872-2067(12)60672-X
    Abstract ( 363 )   [Full Text(HTML)] () PDF (572KB) ( 646 )  

    Ni/Al2O3 catalysts for oxidative dehydrogenation (ODH) of ethane were prepared by impregnation of Al2O3 with nickel acetate or nickel nitrate, and by mechanical mixing of NiO and Al2O3. The Ni-based catalysts were characterized by N2 adsorption-desorption, X-ray diffraction, diffuse reflectance UV-visible diffuse reflectance spectroscopy, and temperature-programmed reduction of hydrogen. The results showed that formation of crystalline NiO particles with a size of < 8 nm and/or non-stoichiometric NiO species in the Ni/Al2O3 catalysts led to more active species in ODH of ethane under the investigated reaction conditions. In contrast, tetrahedral Ni species present in the catalysts led to higher selectivity for ethene. Formation of large crystalline NiO particles (22-32 nm) over Ni/Al2O3 catalysts decreased the selectivity for ethene.

    Aqueous-phase Fischer-Tropsch synthesis catalyzed by cobalt nanoparticles
    Hang Wang, Yuan Kou
    2013, 34 (10):  1914-1925.  DOI: 10.1016/S1872-2067(12)60674-3
    Abstract ( 451 )   [Full Text(HTML)] () PDF (1568KB) ( 868 )  

    Converting syngas to hydrocarbons at much lower temperature with high efficiencies, namely aqueous-phase Fischer-Tropsch synthesis, has great potentials. In this article, we synthesized aqueous-stable cobalt nanoparticles for the reaction. The catalyst has an activity of 7.4 × 10-7 molCO gCo-1 s-1 and C5+ selectivity of 40%, which is the best result in cobalt-catalyzed aqueous-phase Fischer-Tropsch synthesis. The catalyst is recyclable after reaction. We also characterized the catalyst by transmission electron microscopy, X-ray diffraction, and in-situ infrared observation to study the catalyst reconstruction process and boron contamination.

    Photocatalytic hydrogen production under visible-light irradiation on (CuAg)0.15In0.3Zn1.4S2 synthesized by precipitation and calcination
    Guangshan Zhang, Wen Zhang, John C. Crittenden, Yongsheng Chen, Daisuke Minakata, Peng Wang
    2013, 34 (10):  1926-1935.  DOI: 10.1016/S1872-2067(12)60675-5
    Abstract ( 333 )   [Full Text(HTML)] () PDF (663KB) ( 717 )  

    This study investigates the photocatalytic hydrogen production over nanosized (CuAg)0.15In0.3Zn1.4S2 photocatalysts prepared via precipitation and calcination. The photocatalysts were characterized by X-ray diffraction, transmission electron microscopy, scanning electron microscopy, N2 adsorption-desorption, and UV-Vis absorption spectroscopy. The results show that calcination temperature and time significantly influence the crystallinity, specific surface area, and visible-light absorption capacity of the photocatalysts. The photocatalyst activity was studied under visible-light irradiation with KI as the electron donor. The results indicate that the (CuAg)0.15In0.3Zn1.4S2 photocatalyst prepared at a calcination temperature of 600 ℃ for 5 h yields the highest photocatalytic activity (H2 production rate of 1750 μmol g-1 h-1 and quantum yield of 12.8% at 420±5 nm), approximately 6 times larger than that of catalysts prepared without thermal treatment.

    Synthesis of hexahydroquinolines using the new ionic liquid sulfonic acid functionalized pyridinium chloride as a catalyst
    Ardeshir Khazaei, Mohammad Ali Zolfigol, Ahmad Reza Moosavi-Zare, Javad Afsar, Abdolkarim Zare, Vahid Khakyzadeh, Mohammad Hassan Beyzavi
    2013, 34 (10):  1936-1944.  DOI: 10.1016/S1872-2067(12)60678-0
    Abstract ( 337 )   [Full Text(HTML)] () PDF (414KB) ( 765 )  

    Sulfonic acid functionalized pyridinium chloride [pyridine-SO3H]Cl has been synthesized as a novel Brönsted acidic ionic liquid and characterized on the basis of its FT-IR, 1H and 13C NMR, MS, thermogravimetry, and derivative thermogravimetry data. The material has also been used as a highly efficient, homogeneous, and reusable catalyst for the preparation of hexahydroquinolines according to the one-pot multi-component condensation of arylaldehydes, dimedone (5,5-dimethylcyclohexane-1,3-dione), β-ketoesters, and ammonium acetate under solvent-free conditions.

    Removal of high concentrations of formaldehyde in industrial exhaust by catalytic oxidation
    Richu Wei, Honglin Chen, Xiaoming Zhang, Jishuan Suo
    2013, 34 (10):  1945-1950.  DOI: 10.1016/S1872-2067(12)60696-2
    Abstract ( 449 )   [Full Text(HTML)] () PDF (448KB) ( 1142 )  

    A Pt-CeO2/AC catalyst was developed for the removal of high concentrations of formaldehyde (HCHO) in industrial exhaust under mild conditions. The HCHO removal was integrated into a N-(phosphonomethyl)glycine production process to remove in situ the high concentrations of HCHO in its exhaust stream. The HCHO produced and emitted (100-300 mg/m3) in N-(phosphonomethyl)glycine synthesis was completely removed by passage through the catalyst bed. The effects of temperature, space velocity, and HCHO content on removal efficiency were systematically studied. Almost all the HCHO was oxidized at gas hourly space velocities (GHSV) below 20000 h-1, and the HCHO content was decreased to below 0.1 mg/m3, that is, the HCHO conversion rate was 99.10%-100%. When the GHSV was in the range of 30000-50000 h-1 and the catalyst bed temperature was 12 ℃, the HCHO content in the treated gas was still less than 1.5 mg/m3, and the HCHO conversion rate was 97.56%-99.99%. The 1%Pt-4%CeO2/AC catalyst is now in the pilot phase of its use in treating glyphosphate production exhaust gas containing high concentrations of HCHO, and good initial progress has been made. The concentrations of HCHO in the treated industrial exhaust were less than 10 mg/m3, which effectively has no HCHO health hazard, and there are good prospects for industrialization.

    Catalytic properties of nanosized zinc aluminates prepared by green process using Opuntia dilenii haw plant extract
    C. Ragupathi, J. Judith Vijaya, S. Narayanan, L. John Kennedy, Seeram Ramakrishna
    2013, 34 (10):  1951-1958.  DOI: 10.1016/S1872-2067(12)60682-2
    Abstract ( 280 )   [Full Text(HTML)] () PDF (726KB) ( 956 )  

    Various nanosized zinc aluminate (ZnAl2O4) samples were prepared by a conventional and a microwave method both with and without using Opuntia dilenii haw plant extract, and were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), high resolution scanning electron microscopy (HRSEM), energy dispersion scanning (EDX), temperature dependent conductance measurements, thermoelectric power measurements, ultraviolet-visible (UV-Vis) diffuse reflectance spectroscopy, and photoluminescence spectroscopy. The formation of a pure ZnAl2O4 phase was confirmed by XRD and FT-IR. A change in morphology from nanosized plates to nanosized sheets with, respectively, the conventional and microwave heating methods was clearly shown by HRSEM. UV-Vis diffusion reflectance spectroscopy measured the band gaps of ZnAl2O4 nanosized plates and nanosized sheets as 3.5 and 3.9 eV, respectively. The synthesized ZnAl2O4 was single crystalline and has three photoluminescence emissions at 482, 528, and 540 nm. ZnAl2O4 nanosized sheets prepared by the microwave method showed higher catalytic activity for the oxidation of benzyl alcohol (85% conversion) than ZnAl2O4 nanosized plates prepared by the conventional method (60% conversion).