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1Selective catalytic reduction of NO_(x) with NH_(3):opportunities and challenges of Cu-based small-pore zeolites显示文摘Zeolites,as efficient and stable catalysts,are widely used in the environmental catalysis field.Typically,Cu-SSZ-13 with small-pore structure shows excellent catalytic activity for selective catalytic reduction of NO_(x) with ammonia(NH_(3)-SCR)as well as high hydrothermal stability.This review summarizes major advances in Cu-SSZ-13 applied to the NH_(3)-SCR reaction,including the state of copper species,standard and fast SCR reaction mechanism,hydrothermal deactivation mechanism,poisoning resistance and synthetic methodology.The review gives a valuable summary of new insights into the matching between SCR catalyst design principles and the characteristics of Cu^(2+)-exchanged zeolitic catalysts,highlighting the significant opportunity presented by zeolite-based catalysts.Principles for designing zeolites with excellent NH_(3)-SCR performance and hydrothermal stability are proposed.On the basis of these principles,more hydrothermally stable Cu-AEI and Cu-LTA zeolites are elaborated as well as other alternative zeolites applied to NH_(3)-SCR.Finally,we call attention to the challenges facing Cu-based small-pore zeolites that still need to be addressed.Yulong Shan Jinpeng Du Yan Zhang Wenpo Shan Xiaoyan Shi Yunbo Yu Runduo Zhang Xiangju Meng Feng-Shou Xiao Hong He 2021National Science Review2021,8,10:9
2Selective catalytic oxidation of ammonia to nitrogen over orderly mesoporous CuFe_2O_4 with high specific surface area显示文摘Orderly mesoporous CuFe2O4spinel-type mixed oxide with high specific surface area was prepared successfully by a hard-template method in which KIT-6mesoporous silica was selected as the hard template.The KIT-6 hard template and CuFe2O4samples were characterized by X-ray diffraction,X-ray photoelectron spectroscopy,X-ray fluorescence,transmission electron microscopy,scanning electron microscopy,nitrogen physisorption,and hydrogen-temperature programmed reduction.The KIT-6 hard template had perfect crystallization and ordered mesoporous structure with a probable pore distribution of about 9.1 nm,large enough to be filled by the spinel precursor.The mesoporous CuFe2O4spinel oxide synthesized inside the KIT-6 mesopores had a relatively small pore size(4.3 nm),orderly arrangement,and high specific area(194 m2/g).The catalytic activity of the mesoporous CuFe2O4was tested for the selective oxidation of ammonia to nitrogen.The conversion of ammonia reached nearly 100%at 300°C with a nitrogen selectivity as high as 96%.The nitrogen selectivity remained high with increasing temperature and even maintained a value of80%at 600°C.Wenrui Yue Runduo Zhang Ning Liu Biaohua Chen 2014Chinese Science Bulletin2014,59,31:6
3Facile synthesis of Ag-modified manganese oxide for effective catalytic ozone decomposition显示文摘O3 decomposition catalysts with excellent performance still need to be developed. In this study, Ag-modified manganese oxides(AgMnOx) were synthesized by a simple co-precipitation method. The effect of calcination temperature on the activity of MnOx and AgMnOxcatalysts was investigated. The effect of the amount of Ag addition on the activity and structure of the catalysts was further studied by activity testing and characterization by a variety of techniques. The activity of 8%AgMnOxfor ozone decomposition was significantly enhanced due to the formation of the Ag1.8 Mn8 O16 structure, indicating that this phase has excellent performance for ozone decomposition.The weight content of Ag1.8 Mn8 O16 in the 8%AgMnOxcatalyst was only about 33.76%, which further indicates the excellent performance of the Ag1.8 Mn8 O16 phase for ozone decomposition. The H2 temperature programmed reduction(H2-TPR) results indicated that the reducibility of the catalysts increased due to the formation of the Ag1.8 Mn8 O16 structure.This study provides guidance for a follow-up study on Ag-modified manganese oxide catalysts for ozone decomposition.Xiaotong Li Jinzhu Ma Changbin Zhang Runduo Zhang Hong He 2019Journal of Environmental Sciences2019,31,6:5
4Highly active OMS-2 for catalytic ozone decomposition under humid conditions显示文摘Four kinds of cryptomelane-type octahedral molecular sieve(OMS)-2-X(the X represents the molar ratio of KMnO4/MnAc2) were prepared as catalytic materials for ozone decomposition through a one-step hydrothermal reaction of KMnO4 and MnAc2, by changing their molar ratios. These samples were characterized by N2 adsorption–desorption, X-ray di raction(XRD), transmission electron microscopy(TEM), scanning electron microscopy(SEM), temperature programmed reduction by H2(H2-TPR) and X-ray photoelectron spectroscopy(XPS). Among them, the OMS-2-0.7 sample showed the best O3 conversion of 92% under high relative humidity(RH) of 90% and gas hourly space velocity of 585,000 h-1. This was accordingly thought as a possible way for purifying ozone-containing waste gases under high RH atmospheres. The e ciency of ozone decomposition of the prepared OMS-2-X sample was found to be related to specific surface area, particle size, surface oxygen vacancies, and Mn3+ cation amounts. The one-step hydrothermal synthesis was shown to be a simple method to prepare the considerably active OMS-2 solids for ozone decomposition.Bo Peng Wenjing Bao Linlin Wei Runduo Zhang Zhoujun Wang Zhichun Wang Ying Wei 2019Petroleum Science2019,16,4:3
5Detrimental role of residual surface acid ions on ozone decomposition over Ce-modified γ-MnO2under humid conditions显示文摘In the study,the catalyst precursors of Ce-modifiedγ-MnO2 were washed with deionized water until the pH value of the supernatant was 1,2,4 and 7,and the obtained catalysts were named accordingly.Under space velocity of 300,000 hr-1,the ozone conversion over the pH=7 catalyst under dry conditions and relative humidity of 65%over a period of 6 hr was 100%and 96%,respectively.However,the ozone decomposition activity of the pH=2 and 4 catalysts distinctly decreased under relative humidity of 65%compared to that under dry conditions.Detailed physical and chemical characterization demonstrated that the residual sulfate ions on the pH=2 and 4 catalysts decreased their hydrophobicity and then restrained humid ozone decomposition activity.The pH=2 and 4 catalysts had inferior resistance to high space velocity under dry conditions,because the residual sulfate ion on their surface reduced their adsorption capacity for ozone molecules and increased their apparent activation energies,which was proved by temperature programmed desorption of O2 and kinetic experiments.Long-term activity testing,X-ray photoelectron spectroscopy and density functional theory calculations revealed that there were two kinds of oxygen vacancies on the manganese dioxide catalysts,one of which more easily adsorbed oxygen species and then became deactivated.This study revealed the detrimental effect of surface acid ions on the activity of catalysts under humid and dry atmospheres,and provided guidance for the development of highly efficient catalysts for ozone decomposition.Xiaotong Li Jinzhu Ma Changbin Zhang Runduo Zhang Hong He 2020Journal of Environmental Sciences2020,32,5:3
6N/Ce doped graphene supported Pt nanoparticles for the catalytic oxidation of formaldehyde at room temperature显示文摘Pt catalysts with nitrogen-doped graphene oxide (GO) as support and CeO_(2)as promoter were prepared by impregnation method,and their catalytic oxidation of formaldehyde (HCHO) at room temperature was tested.The Pt-CeO_(2)/N-rGO (reduced GO) with a mass fraction of 0.7% Pt and 0.8%CeO_(2)exhibited an excellent catalytic performance with the 100% conversion of HCHO at room temperature.Physicochemical characterization demonstrated that nitrogendoping greatly increased the defect degree and the specific surface area of GO,enhanced the dispersion of Pt and promoted more zero-valent Pt.The synergistic effect between CeO_(2)and Pt was also beneficial to the dispersion of Pt.Nitrogen-doping promoted the production of more Ce3+ions,generating more oxygen vacancies,which was conducive to O_(2)adsorption.As a result,the catalyst exhibited enhanced redox properties,leading to the best catalytic activity.Finally,an attempt to propose the reaction mechanism of HCHO oxidation has been made.Yaodong Guo Zhaoying Di Xiaonan Guo Ying Wei Runduo Zhang Jingbo Jia 2023Journal of Environmental Sciences2023,,3:2
7Ce-promoted Mn/ZSM-5 catalysts for highly efficient decomposition of ozone显示文摘Manganese oxides supported by ZSM-5 zeolite(Mn/ZSM-5) as well as their further modified by Ce promoter were achieved by simple impregnation method for ozone catalytic decomposition. The yCe20Mn/ZSM-5–81 catalyst with 8% Ce loading showed the highest catalytic activity at relative humidity of 50% and a space velocity of 360 L/(g × hr), giving 93% conversion of 600 ppm O_(3) after 5 hr. Moreover, this sample still maintained highly activity and stability in humid air with 50%–70% relative humidity. Series of physicochemical characterization including X-ray diffraction, temperature-programmed technology(NH_3-TPD and H_(2)-TPR), X-ray photoelectron spectroscopy and oxygen isotopic exchange were introduced to disclose the structure-performance relationship. The results indicated that moderate Si/Al ratio(81) of zeolite support was beneficial for ozone decomposition owing to the synergies of acidity and hydrophobicity. Furthermore, compared with 20 Mn/ZSM-5-81, Ce doping could enhance the amount of low valance manganese(such as Mn^(2+) and Mn^(3+)). Besides, the Ce^(3+)/Ce^(4+) ratio of 8Ce20Mn/ZSM-5-81 sample was higher than that of 4Ce_(2)0 Mn/ZSM-5-81. Additionally, the synergy between the MnO_x and CeO_(2) could easily transfer electron via the redox cycle, thus resulting in an increased reducibility at low temperatures and high concentration of surface oxygen. This study provides important insights to the utilization of porous zeolite with high surface area to disperse active component of manganese for ozone decomposition.Linlin Wei Hongxia Chen Ying Wei Jingbo Jia Runduo Zhang 2021Journal of Environmental Sciences2021,33,5:2
8Water vapor sensitivity of nanosized La ( Co, Mn, Fe) 1 - x (Cu,Pd) xO3 perovskites during NO reduction by C3H6 in the presence of oxygen 显示文摘Zhang Runduo Houshang Alamdari Serge Kaliaguine 2007Applied Catalysis B : Environ- mental2007,72,3:1
9Biaohua Chen Lowtemperature selective catalytic reduction of NO with NH3using perovskite-type oxides as the novel catalysts显示文摘Zhang Runduo Luo Na Yang Wei 2013Journal of Molecular Catalysis A:Chemical2013,371,:1
10显示文摘Zhang Runduo Yang Wei Xue Jun 2009Catal Lett2009,,132:1
11Cu - and Pd - substituted nanoseale Fe - based perovskites for selective catalytic reduction of NO by propene显示文摘Zhang Runduo Villanueva A AlamdariL H S 2006J Catal2006,237,2:1
12SCR of NO by propene over nanoscale LaMn1-xCuxO3 perovskites 显示文摘Zhang Runduo Adrian Villanueva Houshang Alamdari 2006Applied Catalysis A : General2006,307,:1
13Cu- and Pal-substituted nanoscale Fe-based perovskites for selective catalytic reduction of NO by propene 显示文摘Zhang Runduo Villanueva Adrian Alamdari Houshang 2006Journal of Catalysis2006,237,2:1
14Science with the 2.5-meter Wide Field Survey Telescope(WFST)显示文摘The Wide Field Survey Telescope(WFST) is a dedicated photometric surveying facility being built jointly by University of Science and Technology of China(USTC) and the Purple Mountain Observatory(PMO). It is equipped with a 2.5-meter diameter primary mirror, an active optics system, and a mosaic CCD camera with 0.73 gigapixels on the primary focal plane for highquality image capture over a 6.5-square-degree field of view. The installation of WFST near the summit of Saishiteng mountain in the Lenghu region is scheduled in summer of 2023, and the operation is planned to start three months later. WFST will scan the northern sky in four optical bands(u, g, r and i) at cadences from hourly/daily in the deep high-cadence survey(DHS) program, to semi-weekly in the wide field survey(WFS) program. During a photometric night, a nominal 30 s exposure in the WFS program will reach a depth of 22.27, 23.32, 22.84, and 22.31(AB magnitudes) in these four bands, respectively, allowing for the detection of a tremendous amount of transients in the low-z universe and a systematic investigation of the variability of Galactic and extragalactic objects. In the DHS program, intranight 90 s exposures as deep as 23(u) and 24 mag(g), in combination with target of opportunity follow-ups, will provide a unique opportunity to explore energetic transients in demand for high sensitivities, including the electromagnetic counterparts of gravitational wave events, supernovae within a few hours of their explosions,tidal disruption events and fast, luminous optical transients even beyond redshift of unity. In addition, the final 6-year co-added images, anticipated to reach g■25.8 mag in WFS or 1.5 mags deeper in DHS, will be of fundamental importance to general Galactic and extragalactic science. The highly uniform legacy surveys of WFST will serve as an indispensable complement to those of the Vera C. Rubin Observatory's Legacy Survey of Space and Time(LSST) that monitors the southern sky.Tinggui Wang Guilin Liu Zhenyi Cai Jinjun Geng Min Fang Haoning He Ji-an Jiang Ning Jiang Xu Kong Bin Li Ye Li Wentao Luo Zhizheng Pan Xuefeng Wu Ji Yang Jiming Yu Xianzhong Zheng Qingfeng Zhu Yi-Fu Cai Yuanyuan Chen Zhiwei Chen Zigao Dai Lulu Fan Yizhong Fan Wenjuan Fang Zhicheng He Lei Hu Maokai Hu Zhiping Jin Zhibo Jiang Guoliang Li Fan Li Xuzhi Li Runduo Liang Zheyu Lin Qingzhong Liu Wenhao Liu Zhengyan Liu Wei Liu Yao Liu Zheng Lou Han Qu Zhenfeng Sheng Jianchun Shi Yiping Shu Zhenbo Su Tianrui Sun Hongchi Wang Huiyuan Wang Jian Wang Junxian Wang Daming Wei Junjie Wei Yongquan Xue Jingzhi Yan Chao Yang Ye Yuan Yefei Yuan Hongxin Zhang Miaomiao Zhang Haibin Zhao Wen Zhao 2023Science China(Physics,Mechanics & Astronomy)2023,66,10:1
15Low-temperature selective catalytic reduction of NO with NH 3 using perovskite-type oxides as the novel catalysts显示文摘Runduo Zhang Na Luo Wei Yang Ning Liu Biaohua Chen 2013A, Chemical2013,,:1
16Kinetics of selective catalytic reduction of NO with NH2 on wiremesh-honeycomb显示文摘Zhang RunDuo Quan Xie Yang Feng Lin 2002Journal of Dalian University of Technology2002,42,2:1
17Free energy perturbation(FEP)-guided scaffold hopping显示文摘Scaffold hopping refers to computer-aided screening for active compounds with different structures against the same receptor to enrich privileged scaffolds,which is a topic of high interest in organic and medicinal chemistry.However,most approaches cannot efficiently predict the potency level of candidates after scaffold hopping.Herein,we identified potent PDE5 inhibitors with a novel scaffold via a free energy perturbation(FEP)-guided scaffold-hopping strategy,and FEP shows great advantages to precisely predict the theoretical binding potenciesΔGFEPbetween ligands and their target,which were more consistent with the experimental binding potenciesΔGEXP(the mean absolute deviations|ΔGFEP-ΔGEXP|<2 kcal/mol)than thoseΔGMM-PBSAorΔGMM-GBSApredicted by the MM-PBSA or MM-GBSA method.Lead L12 had an IC_(50) of 8.7 nmol/L and exhibited a different binding pattern in its crystal structure with PDE5 from the famous starting drug tadalafil.Our work provides the first report via the FEPguided scaffold hopping strategy for potent inhibitor discovery with a novel scaffold,implying that it will have a variety of future applications in rational molecular design and drug discovery.Deyan Wu Xuehua Zheng Runduo Liu Zhe Li Zan Jiang Qian Zhou Yue Huang Xu-Nian Wu Chen Zhang Yi-You Huang Hai-Bin Luo 2022Acta Pharmaceutica Sinica B2022,12,3:1
18Catalytic purification of acrylonitrile-containing exhaust gases from petrochemical industry by metal-doped mesoporous zeolites显示文摘Runduo Zhang Dongjun Shi Ning Liu Biaohua Chen Lianghua Wu Libin Wu Weimin Yang 2015Catalysis Today2015,,:1
19Cu- and Pd-substituted nanoscale Fe-based perovskites for selective catalytic reduction of NO by propene显示文摘Runduo Zhang Adrian Villanueva Houshang Alamdari Serge Kaliaguine 2006Journal of Catalysis2006,,2:1
20SCR of NO by propene over nanoscale LaMnl -xCuO3 perovskites显示文摘Zhang Runduo Adrian Villanueva Houshang Alamdari et aI 2006Applied Catalysis A: General2006,307,:1
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