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32篇 您的检索式:作者名="Jiguang Deng"
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1Rare earth oxides and their supported noble metals in application of environmental catalysis显示文摘Volatile organic compounds(VOCs),methane,carbon monoxide,soot,automotive exhaust,and nitrogen oxides are harmful to the atmosphere and human health.It is urgent to strictly control their emissions.Heterogeneous catalysis is an effective pathway for the removal of these pollutants,and the critical issue is the development of novel and high-performance catalysts.In this review,we briefly summarize the preparation methods,physicochemical properties,catalytic activities,and related reaction mechanisms for the above pollutants removal of the rare earth oxides,mixed rare earth oxide,rare earth oxidesupported noble metal,and mixed rare earth oxide-supported noble metal catalysts that have been investigated by our group and other researchers.It was found that catalytic performance was associated with the factors,such as specific surface area,pore structure,particle size and dispersion,adsorbed oxygen species concentration,reducibility,reactant activation ability or interaction between metal nanoparticles and support.Furthermore,we also envision the development trend of such a topic in future work.Zhiquan Hou Wenbo Pei Xing Zhang Kunfeng Zhang Yuxi Liu Jiguang Deng Lin Jing Hongxing Dai 2020Journal of Rare Earths2020,38,8:10
2Concurrent catalytic removal of typical volatile organic compound mixtures over Au-Pd/α-MnO2 nanotubes显示文摘α-MnO_2 nanotubes and their supported Au-Pd alloy nanocatalysts were prepared using hydrothermal and polyvinyl alcohol-protected reduction methods, respectively. Their catalytic activity for the oxidation of toluene/m-xylene, acetone/ethyl acetate, acetone/m-xylene and ethyl acetate/m-xylene mixtures was evaluated. It was found that the interaction between Au-Pd alloy nanoparticles and α-MnO_2 nanotubes significantly improved the reactivity of lattice oxygen, and the 0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst outperformed the α-MnO_2 nanotube catalyst in the oxidation of toluene, m-xylene, ethyl acetate and acetone. Over the0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst,(i) toluene oxidation was greatly inhibited in the toluene/m-xylene mixture, while m-xylene oxidation was not influenced;(ii) acetone and ethyl acetate oxidation suffered a minor impact in the acetone/ethyl acetate mixture; and(iii) m-xylene oxidation was enhanced whereas the oxidation of the oxygenated VOCs(volatile organic compounds) was suppressed in the acetone/m-xylene or ethyl acetate/m-xylene mixtures. The competitive adsorption of these typical VOCs on the catalyst surface induced an inhibitive effect on their oxidation, and increasing the temperature favored the oxidation of the VOCs. The mixed VOCs could be completely oxidized into CO_2 and H_2 O below 320°C at a space velocity of 40,000 m L/(g·hr). The 0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst exhibited high catalytic stability as well as good tolerance to water vapor and CO_2 in the oxidation of the VOC mixtures. Thus, the α-MnO_2 nanotube-supported noble metal alloy catalysts hold promise for the efficient elimination of VOC mixtures.Yunsheng Xia Lu Xia Yuxi Liu Tao Yang Jiguang Deng Hongxing Dai 2018Journal of Environmental Sciences2018,30,2:7
3Hydrothermal fabrication and visible-light-driven photocatalytic properties of bismuth vanadate with multiple morphologies and/or porous structures for Methyl Orange degradation显示文摘Monoclinic BiVO4 with multiple morphologies and/or porous structures were fabricated using the hydrothermal strategy. The materials were characterized by means of the XRD, Raman, TGA/DSC, SEM, XPS, and UV-Vis techniques. The photocatalytic activities of the BiVO4 materials were evaluated for the degradation of Methyl Orange under visible-light irradiation. It is observed that pH value and surfactant exerted a great effect on the morphology and pore structure of the BiVO4 product. Spherical BiVO4 with porous structures, flower-cluster-like BiVO4, and flower-bundle-like BiVO4 were generated hydrothermally at 100°C with poly(vinyl pyrrolidone) (PVP) and urea (pH = 2) and at 160°C with NaHCO3 (pH = 7 and 8), respectively. The PVP-derived BiVO4 showed much higher surface areas (5.0-8.4 m2/g) and narrower bandgap energies (2.45-2.49 eV). The best photocatalytic performance of the spherical BiVO4 material with a surface area of 8.4 m2/g was associated with its higher surface area, narrower bandgap energy, higher surface oxygen vacancy density, and unique porous architecture.Haiyan Jiang Hongxing Dai Xue Meng Lei Zhang Jiguang Deng Yuxi Liu Chak Tong Au 2012Journal of Environmental Sciences2012,24,3:5
4Porous FeO_x/BiVO_(4-δ)S_(0.08): Highly efcient photocatalysts for the degradation of Methylene Blue under visible-light illumination显示文摘Porous S-doped bismuth vanadate with an olive-like morphology and its supported iron oxide(y wt.% FeOx/BiVO4 δS0.08, y =0.06, 0.76, and 1.40) photocatalysts were fabricated using the dodecylamine-assisted alcohol-hydrothermal and incipient wetness impregnation methods, respectively. It is shown that the y wt.% FeOx/BiVO4 δS0.08photocatalysts contained a monoclinic scheetlite BiVO4 phase with a porous olive-like morphology, a surface area of 8.8–9.2 m2/g, and a bandgap energy of 2.38–2.42 eV. There was co-presence of surface Bi5+, Bi3+, V5+, V3+, Fe3+, and Fe2+species in y wt.% FeOx/BiVO4 δS0.08. The 1.40 wt.% FeOx/BiVO4 δS0.08sample performed the best for Methylene Blue degradation under visible-light illumination. The photocatalytic mechanism was also discussed. We believe that the sulfur and FeOx co-doping, higher oxygen adspecies concentration, and lower bandgap energy were responsible for the excellent visible-light-driven catalytic activity of 1.40 wt.% FeOx/BiVO4 δS0.08.Zhenxuan Zhao Hongxing Dai Jiguang Deng Yuxi Liu Yuan Wang Xinwei Li Guangmei Bai Baozu Gao Chak Tong Au 2013Journal of Environmental Sciences2013,25,10:4
5Synthesis and characterization of wormhole-like mesoporous Ce_(0.6)Zr_(0.35)Y_(0.05)O_2 solid solutions显示文摘Nanoparticles of Ce0.6Zr0.35Y0.05O2 (CZY) solid solution have been prepared by the CTAB (hexadecyl-trimethyl ammonium bromide), CTAB-EG (ethylene glycol) templating, and CTAB-EG-NaCl (in which the pores of the precursor synthesized by the CTAB-EG method is filled by a certain amount of NaCl) method, respectively. The physical properties of these materials were characterized by means of tech-niques such as X-ray diffraction (XRD), high resolution scanning electron microscopy (HRSEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), and N2 adsorp-tion-desorption measurements. The CZY samples synthesized by the above three methods display wormhole-like mesoporous morphology and cubic crystal structures. The materials are narrow in pore size distribution (averaged pore diameter = 5.3―7.1 nm), high in surface areas (95―119 m2/g), and large in pore volumes (0.16―0.18 cm3/g). It has been demonstrated that the introduction of NaCl is capable of retaining the pore structures of solid nanomaterials at high-temperature calcination.WANG GuoZhi ZHANG Lei DENG JiGuang DAI HongXing HE Hong ZI XueHong 2007Chinese Science Bulletin2007,52,2:4
6Preparation and catalytic performance of Fe-SBA-15 and FeO_x/SBA-15 for toluene combustion显示文摘High-surface-area and well-ordered mesoporous Fe-incorporated SBA-15(xFe-SBA-15)and SBA-15-supported FeOx(yFeOx/SBA-15)with the Fe surface density between 0.09 to 1.11 Fe-atom/nm2have been prepared using the one-step synthesis and incipient wetness impregnation methods,respectively.Physicochemical properties of these materials were characterized by means of numerous techniques,and their catalytic activities for the combustion of toluene were evaluated.It is found that the xFe-SBA-15 and yFeOx/SBA-15 samples possessed rod-or chain-like morphologies.The Fe species were of high dispersion when the Fe surface density was lower than0.76 Fe-atom/nm2in xFe-SBA-15 and 0.64 Fe-atom/nm2in yFeOx/SBA-15.At a similar Fe surface density and space velocity,the xFe-SBA-15 catalysts showed better activity than the yFeOx/SBA-15 catalysts,in which the xFe-SBA-15 catalyst with Fe surface density 0.59 Fe-atom/nm2performed the best.It is concluded that the good performance of the xFe-SBA-15 sample with Fe surface density0.59 Fe-atom/nm2was associated with its large surface area,high Fe species dispersion,and good low-temperature reducibility.Yujuan Zhang Jiguang Deng Lei Zhang Hongxing Dai 2014Chinese Science Bulletin2014,59,31:4
7Surfactant-aided hydrothermal preparation of La(2-x)Sr_xCuO_4 single crystallites and their catalytic performance on methane combustion显示文摘Perovskite-like oxide La2-xSrxCuO4 (x = 0, 1) single crystallites with microrod-like morphologies and tetragonal crystal structures were prepared hydrothermally at 240°C with poly(ethylene glycol) (PEG) or hexadecyltrimethyl ammonium bromide (CTAB) as a surfactant and after calcination at 850°C. The physicochemical properties of the materials were characterized by means of XRD, BET, SEM, TEM/SAED (selected-area electron diffraction), XPS and H2-TPR techniques. It is found that doping Sr2+ to La2CuO4 lattice enhanced the catalytic activity for methane combustion and the LaSrCuO4 catalyst derived from PEG is the best among the tested ones. It is concluded that factors, such as adsorbed oxygen species concentration, reducibility and surface area, determined the catalytic performance of such single-crystalline materials.Lei Zhang Yue Zhang Jiguang Deng Hongxing Dai 2012Journal of Natural Gas Chemistry2012,21,1:4
8Au-Pd/mesoporous Fe_2O_3:Highly active photocatalysts for the visible-light-driven degradation of acetone显示文摘Three-dimensionally ordered mesoporous Fe_2O_3(meso-Fe_2O_3) and its supported Au, Pd,and Au-Pd alloy(xA uP dy/meso-Fe_2O_3; x = 0.08–0.72 wt.%; Pd/Au molar ratio(y) = 1.48–1.85)photocatalysts have been prepared via the KIT-6-templating and polyvinyl alcohol-protected reduction routes, respectively. Physical properties of the samples were characterized, and their photocatalytic activities were evaluated for the photocatalytic oxidation of acetone in the presence of a small amount of H_2O_2 under visible-light illumination. It was found that the meso-Fe_2O_3 was rhombohedral in crystal structure. The as-obtained samples displayed a high surface area of 111.0–140.8 m^2/g and a bandgap energy of 1.98–2.12 eV. The Au, Pd and/or Au–Pd alloy nanoparticles(NPs) with a size of 3–4 nm were uniformly dispersed on the surface of the meso-Fe_2O_3 support. The 0.72 wt.% AuP d1.48/meso-Fe_2O_3 sample performed the best in the presence of 0.06 mol/L H_2O_2 aqueous solution, showing a 100% acetone conversion within4 hr of visible-light illumination. It was concluded that the good performance of 0.72 wt.%AuPd_(1.48)/meso-Fe_2O_3 for photocatalytic acetone oxidation was associated with its ordered mesoporous structure, high adsorbed oxygen species concentration, plasmonic resonance effect between AuPd_(1.48) NPs and meso-Fe_2O_3, and effective separation of the photogenerated charge carriers. In addition, the introduction of H_2O_2 and the involvement of the photo-Fenton process also played important roles in enhancing the photocatalytic activity of 0.72 wt.%AuPd_(1.48)/meso-Fe_2O_3.Hongxia Lin Yuxi Liu Jiguang Deng Kunfeng Zhang Xing Zhang Shaohua Xie Xingtian Zhao Jun Yang Zhuo Han Hongxing Dai 2018Journal of Environmental Sciences2018,30,8:2
9A comparative investigation of NdSrCu_(1-x) Co_x O_(4-δ) and Sm_(1.8) Ce_(0.2) Cu_(1-x) Co_x O_(4-δ) (x:0–0.4) for NO decomposition显示文摘A series of single-phase T-structured NdSrCu 1-x Co x O 4-δ with oxygen vacancies and T -structured Sm 1.8 Ce 0.2 Cu 1-x Co x O 4-δ (x: 0–0.4) with oxygen excess were prepared using ultrasound-assisted citric acid complexing method, and characterized by means of techniques such as thermogravimetric analysis and NO temperature-programmed desorption (NO-TPD). The catalytic activities of these materials were evaluated for the decomposition of NO. It was found that the NdSrCu 1-x Co x O 4-δ catalysts were of oxygen vacancies whereas the Sm 1.8 Ce 0.2 Cu 1-x Co x O 4-δ ones possessed excessive oxygen (i.e., over-stoichiometric oxygen); with a rise in Co doping level, the oxygen vacancy density of NdSrCu 1-x Co x O 4-δ decreased while the over-stoichiometric oxygen amount of Sm 1.8 Ce 0.2 Cu 1-x Co x O 4-δ increased. The NO-TPD results revealed that NO could be activated much easier over the oxygen-deficient perovskite-like oxides than over the oxygen-excessive perovskite-like oxides, with the NdSrCuO 3.702 catalyst showing the best efficiency in activating NO molecules. Under the conditions of 1.0% NO/helium, 2800 hr -1 , and 600–900°C, the catalytic activity of NO decomposition followed the order of NdSrCuO 3.702 > NdSrCu 0.8 Co 0.2 O 3.736 > NdSrCu 0.6 Co 0.4 O 3.789 > Sm 1.8 Ce 0.2 Cu 0.6 Co 0.4 O 4.187 > Sm 1.8 Ce 0.2 Cu 0.8 Co 0.2 O 4.104 > Sm 1.8 Ce 0.2 CuO 4.045 , in concord with the sequence of decreasing oxygen vacancy or oxygen excess density. Based on the results, we concluded that the higher oxygen vacancy density and the stronger Cu 3+ /Cu 2+ redox ability of NdSrCu 1-x Co x O 4-δ account for the easier activation of NO and consequently improve the catalytic activity of NO decomposition over the catalysts.Jiguang Deng Lei Zhang Yunsheng Xia Hongxing Dai Hong He 2010Journal of Environmental Sciences2010,22,3:2
10Research on design and simulation of FM/cw lidar system显示文摘ZHAO Jiguang ZHANG Zhiquan DENG Chen 2009Laser Sensing and Imaging2009,7382,:1
11Immobilization of antimony in soil and groundwater using ferro-magnesium bimetallic organic frameworks显示文摘Sb(Ⅲ) is often detected in contaminated soil and groundwater. Hence, high-efficiency technology is needed. In this study, bimetallic organic frameworks were used for the first time to immobilize Sb(Ⅲ) from contaminated soil and groundwater. The materials were synthesized by the hydrothermal method. Both ends of the prepared material were hexagonal tip rods,and the length became shorter as the ratio of Fe/Mg decreased. The bimetallic organic framework with a Fe/Mg feeding ratio of 0.5 was the optimum material for Sb(Ⅲ) removal, which could effectively immobilize Sb(Ⅲ). The adsorption isotherm was fitted well with the Freundlich model, and the optimal adsorption capacity can reach 106.97 mg/g. The adsorption capacity of 84% can be completed in 10 min, which conformed to the pseudo-second-order kinetics. The Fe^(3+)could enhance the stability of the material, and the Mg^(2+)was conducive to freeing up adsorption sites for binding Sb(Ⅲ) and forming stable chemical adsorption. Ion exchange is the predominant mechanism to remove Sb(Ⅲ). After 14 days of remediation of Sb(Ⅲ) contaminated soil, the Toxicity Characteristic Leaching Procedure(TCLP)-leached concentrations of Sb(Ⅲ) were reduced by 86%, 91% and 94% when the material dosages were1%, 2% and 3%, respectively. Immobilization of Sb(Ⅲ) in soil resulted in a conversion of antimony speciation from more easily bioavailable species to less bioavailable species, further contributing to reduce the environmental risk of antimony. The results indicate that ferromagnesium bimetallic organic frameworks may serve as a kind of promising materials for the immobilization of Sb(Ⅲ) in contaminated soil and groundwater.Le Yuan JianleWang Zuqi Zhong Jiguang Li Hong Deng 2023Journal of Environmental Sciences2023,,3:1
12Single-Crystalline La0.6Sr0.4CoO3-δ Nanowires/Nanorods Derived Hydrothermally Without the Use of a Template: Catalysts Highly Active for Toluene Complete Oxidation显示文摘Jiguang Deng Lei Zhang Hongxing Dai Hong He Chak Tong Au 2008Catalysis Letters (-)2008,,3:1
13Mesoporous cobalt monoxide-supported platinum nanoparticles:Superior catalysts for the oxidative removal of benzene显示文摘Mesoporous Co3 O4(meso-Co3 O4)-supported Pt(0.53 wt.%Pt/meso-Co304)was synthesized via the KIT-6-templating and polyvinyl alcohol(PVA)-assisted reduction routes.Mesoporous CoO(meso-CoO)was fabricated through in situ reduction of meso-Co304 with glycerol,and the 0.18-0.69 wt.%Pt/meso-CoO samples were generated by the PVA-assisted reduction method.Meso-Co3 O4 and meso-CoO were of cubic crystal structure and the Pt nanoparticles(NPs)with a uniform size of ca.2 nm were well distributed on the mesoCo3 O4 or meso-CoO surface.The 0.56 wt%Pt/meso-CoO(0.56 Pt/meso-CoO)sample performed the best in benzene combustion(T50%=156℃and T90%=186℃at a space velocity of 80,000 mL/(g h)).Introducing water vapor or C02 with a certain concentration led to partial deactivation of 0.56 Pt/meso-CoO and such a deactivation was reversible.We think that the superior catalytic activity of 0.56 Pt/meso-CoO was intimately related to its good oxygen activation and benzene adsorption ability.Jun Yang Yutong Xue Yuxi Liu Jiguang Deng Xiyun Jiang Huan Chen Hongxing Dai 2020Journal of Environmental Sciences2020,32,4:1
14Insitu hydrothermally synthesized mesoporous LaCoO3 /SBA-15 catalysts: high activity for the complete oxida-tion of toluene and ethyl acetate显示文摘DENG Jiguang ZHANG Lei DAI Hongxing 2009Applied CatalysisA: General2009,352,12:1
15Glucoseassisted hydrothermal preparation and catalytic performance of porous LaFeO3 for toluene combustion显示文摘Ji Kemeng Dai Hongxing Deng Jiguang 2013Journal of Solid State Chemistry2013,199,:1
16Single-crystalline mesoporous CaO supported Cr-V binary oxides: Highly ac tive catalysts for the oxidative dehydrogenation of isobutene 显示文摘Deng Jiguang Zhang Lei Liu Caixin 2011Catalysis Today2011,164,:1
17In situ poly (methyl methacrylate)-templafing generation and excellent catalytic per- formance of MnOJ3DOM LaMnO3 for thecombustion of toluene and methanol 显示文摘Yuxi Liu Hongxing Dai Jiguang Deng 2013Applied Catalysis B : Environmental2013,,:1
18Surfactant-assisted solvo- or hydrothermal fabrication and characterization of high-surface-area porous calcium carbonate with multiple morphologies显示文摘Zhenxuan Zhao Lei Zhang Hongxing Dai Yucheng Du Xue Meng Ruzhen Zhang Yuxi Liu Jiguang Deng 2010Microporous and Mesoporous Materials2010,,1:1
19Controlled synthesis, characterization, and morphology-dependent reducibility of ceria-zirconia-yt- tria solid solutions with nanorod-like, microspherical, microbowknot-like, and micro-octahedral shapes 显示文摘Zhang Yujuan Zhang Lei Deng Jiguang 2009Inorg Chem2009,48,5:1
20In situ hydro- thermally synthesized mesoporous LaCoO3/SBA-15 catalysts: High activity for the complete oxidation of toluene and ethyl ace- tate 显示文摘Jiguang Deng Lei Zhang Hongxing Dai 2009Applied Catalysis A: General2009,352,12:1
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