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Nanomaterials · 2020 ·Vol. 10 ·期 11 ·2170 · IF 4.324

Catalytic Performances of Cu/MCM-22 Zeolites with Different Cu Loadings in NH3-SCR

Jialing Chen,Gang Peng,Tingyu Liang,Wenbo Zhang,Wei Zheng,Haoran Zhao,Li Guo,Xiaoqin Wu

The NH3-SCR activities and hydrothermal stabilities of fivexCu/MCM-22 zeolites with different Cu loadings (x= 2–10 wt%) prepared by incipient wetness impregnation method were systematically investigated. The physicochemical properties ofxCu/MCM-22 zeolites were analyzed by XRD, nitrogen physisorption, ICP-AES, SEM, NH3-TPD, UV-vis, H2-TPR and XPS experiments. The Cu species existing inxCu/MCM-22 are mainly isolated Cu2+, CuOxand unreducible copper species. The concentrations of both isolated Cu2+and CuOxspecies inxCu/MCM-22 increase with Cu contents, but the increment of CuOxspecies is more distinct, especially in high Cu loadings (>4 wt%). NH3-SCR experimental results demonstrated that the activity ofxCu/MCM-22 is sensitive to Cu content at low Cu loadings (≤4 wt%). When the Cu loading exceeds 4 wt%, the NH3-SCR activity ofxCu/MCM-22 is irrelevant to Cu content due to the severe pore blockage effects caused by aggregated CuOxspecies. Among the fivexCu/MCM-22 zeolites, 4Cu/MCM-22 with moderate Cu content has the best NH3-SCR performance, which displays higher than 80% NOxconversions in a wide temperature window (160–430 °C). Furthermore, the hydrothermal aging experiments (xCu/MCM-22 was treated at 750 °C for 10 h under 10% water vapor atmosphere) illustrated that all thexCu/MCM-22 zeolites exhibit high hydrothermal stability in NH3-SCR reactions.Keywords:Cu/MCM-22;NH3-SCR;Cu loading;hydrothermal aging

CAS / MDL: 111-49-9
研究领域: 催化化学 · 环境科学
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Nanomaterials · 2021 ·Vol. 11 ·期 9 ·2369 · IF 5.076

Oxidative Desulfurization Catalyzed by Phosphotungstic Acid Supported on Hierarchical Porous Carbons

Bao Wang,Lihua Kang,Mingyuan Zhu

A hierarchical porous carbon material (HPC) with an ultra-high specific surface area was synthesized with sisal fiber (SF) as a precursor, and then H3PW12O40·24H2O (HPW) was immobilized on the support of SF-HPC by a simple impregnation method. A series characterization technology approved that the obtained SF-HPC had a high surface area of 3152.46 m2g−1with micropores and macropores. HPW was well-dispersed on the surface of the SF-HPC support, which reduced the loading of HPW to as low as 5%. HPW/SF-HPW showed excellent catalytic performance for oxidative desulfurization, and the desulfurization rate reached almost 100% under the optimal reaction conditions. The desulfurization rate of HPW/SF-HPW could be maintained at above 94% after four recycles.Keywords:oxidative desulfurization;hierarchical porous carbon;HPW loading;dispersion

研究领域: 材料科学 · 催化化学
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2024 · IF 8.1

The impact of support selection and Co loading amount on the catalytic performance for methane combustion

Juntian Niu,Ziwei Jin,Baihe Guo,Haiyu Liu,Yan Jin,Jingyu Ran

Methane (CH 4 ) is a key component of natural gas and is essential for energy production and utilization. However, due to its strong greenhouse effect, efficient catalytic combustion methods are needed to convert it into CO 2 and H 2 O. This study systematically evaluates the catalytic performance of Co, CoO, and Co 3 O 4 in methane catalytic combustion, particularly highlighting the superior activity of Co 3 O 4 . To improve catalytic efficiency, this paper examines the effects of SiO 2 , Al 2 O 3 , and CeO 2 as support materials using co-precipitation and impregnation methods. The results show a significant improvement in the catalytic activity of Co 3 O 4 supported on CeO 2 , attributed to CeO 2 's unique redox properties and high oxygen storage capacity. Additionally, the study explores the impact of different loading amounts (5%, 10%, 15%, 20%) of Co 3 O 4 (x)-CeO 2 catalysts on their performance. The optimal 10%wt Co 3 O 4 –CeO 2 catalyst achieves methane conversion rates of 10%, 50%, and 90% at temperatures of 376 °C, 473 °C, and 578 °C, respectively, demonstrating exceptional stability during a 20-h stability test and the ability to adapt to fluctuations in CH 4 concentrations in low-oxygen environments, while also exhibiting significant catalytic activity across a range of methane concentrations from 0.5% to 2.5%. These findings provide important theoretical and experimental guidance for the application of cobalt-based catalysts in CH 4 combustion, paving the way for future catalyst design and optimization.

研究领域: 化学工程 · 环境科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

Effect of Cu loading on the structure and catalytic properties of Cu/SBA-15 for the hydrogenation of furfural to furfuryl alcohol

Jicheng Wang,Yanhong Quan,Linjie Li,Shunan Yin,Xinxin Ding,Jun Ren

A series of Cu/SBA-15 catalysts with different Cu loadings are prepared by the ammonia evaporation method for the liquid-phase hydrogenation of furfural (FF) to furfuryl alcohol (FA). The results show that the supported Cu loading influences the structure and catalytic activity during FF hydrogenation. The 20Cu/SBA-15 catalyst shows the optimum performance with 99.3 % FF conversion, 99.0 % selectivity to FA, nearly pure FA product, and a turnover frequency reaching up to 81.7h −1 . The effect of Cu loading can be related to Cu dispersion and the interaction between the metal and support, which further promotes the surface Cu + /Cu 0 ratio. Additionally, the correlation of FF conversion with Cu + /Cu 0 ratio confirms that the excellent performance of 20Cu/SBA-15 is mainly derived from the synergy of Cu + and Cu 0 species, although the range of performance is not large. Finally, the optimal reaction conditions are screened using a reaction temperature of 150 °C, a reaction pressure of 4 MPa, a catalyst dosage of 0.1 g, and a reaction time of 60 min. The present study confirms that the Cu loading has a significant effect on the structure of Cu/SBA-15 and nearly pure objective FF product can be feasibly obtained with an appropriate Cu support in the synthesis of FA from FF hydrogenation.

CAS / MDL: 10031-43-3
研究领域: 催化化学 · 材料科学
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2020 · IF 4.939

Enhancing selectivity and reducing cost for dehydrogenation of dodecahydro-N-ethylcarbazole by supporting platinum on titanium dioxide

Xiang Gong,Zhao Jiang,Tao Fang

N-ethylcarbazole/dodecahydro-N-ethylcarbazole (NECZ/12H-NECZ) was a promising system for hydrogen storage applications. 1.0 wt% Pt/TiO 2 was regarded as the optimal loading in Pt/TiO 2 catalyst applied in the 12H-NECZ dehydrogenation reaction. The hydrogen release amount, selectivity to NECZ and TOF of 12H-NECZ dehydrogenation are 5.75 wt %, 98% and 229.73 min −1 at 453 K. Compared with the commercial 5.0 wt% Pd and Pt-based catalysts, it exhibited very high activity, selectivity and stability for 12H-NECZ dehydrogenation with low Pt loading. Combined with the XRD , XPS , HRTEM , TPR analysis, it was indicated that the enhanced catalytic performance was due to the SMSI (strong metal-supporting interaction) between Pt and TiO 2 support, which accelerated the rate-limiting step and enhanced the whole dehydrogenation reaction. This work may be beneficial for the commercial application of Pt/TiO 2 catalysts in the Liquid Organic Hydrogen Carrier (LOHC) system.

研究领域: 化学工程 · 材料科学
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Journal of the Taiwan Institute of Chemical Engineers · 2024 · IF 5.5

Influence of MoS2 loading on the formation and hydrogenation effect of loaded monolayer molybdenum disulfide

Xiaoning Zhang,Buning Chen,Jianwei Wang,Yusheng Zhou,Xueli Huang,He Huang

Background Molybdenum disulfide is one of the main catalysts used in slurry-bed reactors. However, monolayer molybdenum disulfide with high hydrogenation activity is extremely difficult to obtain owing to the van der Waals forces between layers. Methods MoTi-X catalysts with different MoS 2 loadings were synthesized using a hydrothermal method. Changes in the active phase of MoTi-X during hydrogenation were also analyzed by TEM, XPS, and Raman spectroscopy. Significant findings MoTi-X catalysts synthesized by a two-step hydrothermal process allowed for the simultaneous generation of monolayer MoS 2 and hydrogenation. The results of the phenanthrene-phenol co-hydrogenation system showed that the different active sites on MoS 2 were responsible for its Hydrogenation and Hydrodeoxygenation properties. Using MoTi-X to catalyze coal tar (CT) hydrogenation, the total content of gasoline and diesel fractions was increased by 11.3 %, which is 3.3 times more effective than industrial four-stage hydrogenation. The average molecular mass, viscosity, and density of the coal tar were reduced by 35 %, 96 %, and 6 %, respectively. The application of MoTi-X catalysts for CT hydrogenation can fill the gap in the research on CT slurry-bed hydrogenation catalysts and improve the competitiveness of enterprises.

研究领域: 材料科学 · 化学工程
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2020 · IF 7.489

Effect of Pd loading on ZrO2 support resulting from pyrolysis of UiO-66: Application to CO oxidation

Fukun Bi,Xiaodong Zhang,Shang Xiang,Yunyun Wang

The effect of Pd loading (0.25, 0.5 and 1.0 wt%) and ZrO 2 support calcined at diverse temperatures (600, 700 and 800 °C) by pyrolysis of UiO-66 was investigated for CO oxidation in this work, respectively. The physicochemical properties of the samples were characterized by various characterization methods. The XRD results exhibited that all ZrO 2 support possessed mixed crystalline phase, the monoclinic ZrO 2 and tetragonal ZrO 2 . And the calcination temperature had a big impact on the composition of ZrO 2 supports. Pyrolysis of UiO-66 at high temperature was favorable for the formation of monoclinic ZrO 2 . Additionally, the introduction of Pd was induced the phase conversion from tetragonal to monoclinic of ZrO 2 . The order of catalytic efficiency was as follows: 0.5Pd/Zr-700 > 0.5Pd/Zr-600 > 0.5Pd/Zr-800. Moreover, 0.5Pd/Zr-700 presented high stability and great reusability. The good catalytic performance of 0.5Pd/Zr-700 was ascribed to the better reduction ability at low temperature and high O ads /O lat and Pd 0 /Pd 2+ on the surface. Importantly, the reaction pathway of CO oxidation over the 0.5Pd/Zr-700 was exposed.

研究领域: 催化化学 · 材料科学
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RENEWABLE ENERGY · 2022 · IF 8.634

Promoted ketonization of bagasse pyrolysis gas over red mud-based oxides

Shanshan Shao,Pengfei Zhang,Xianliang Xiang,Xiaohua Li,Huiyan Zhang

Ketonization of bagasse pyrolysis gas was performed over red mud-based oxides. The maximum yield of ketones in the catalytic conversion of bagasse pyrolysis gas over original red mud was 18.66% at 420 °C. To promote the oxidability of red mud and obtain a higher yield of ketones, the effect of metal oxides (CeO 2 , MnO 2 , TiO 2 , CaO, ZrO 2 ) loading and loading amount of CeO 2 on red mud on ketonization of bagasse pyrolysis gas were studied. The highest yield of ketones of 27.86% was obtained over red mud-based oxides with 40 wt% CeO 2 loading. The oxidability of the catalyst was enhanced greatly by the high loading of CeO 2 , leading to the peroxidation of acetone as the side reaction. To control the oxidability and cut costs, bimetallic oxides were loaded on red mud. The yield of ketones reached 30.12% over the composite red mud catalyst with the loading of 20 wt% CeO 2 and 20 wt% MnO 2 . The rough coating of MnO 2 on the surface of red mud was beneficial to the loading of CeO 2 , resulting in smaller and more uniform grains. This study provides the efficient utilization of red mud and biomass as solid wastes for high-valued chemicals and fuels.

研究领域: 能源与环境科学 · 催化化学
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FISH & SHELLFISH IMMUNOLOGY · 2023 · IF 4.7

Adamantoyl chloride inhibited replication of the largemouth bass virus via enhanced immunity and inhibition of apoptosis

Mengmeng Wang,Bin Yang,Tao Liu,Pengfei Li,Shangjie Bai,Zhengyang Zhou,Xiang Liu,Maosheng He,Fei Ling,Gaoxue Wang

The largemouth bass virus (LMBV) is a commonly encountered pathogen in aquaculture and presents significant challenges to development of the largemouth bass industry due to the lack of effective treatment methods. Here, the inhibitory potential and underlying mechanisms of adamantoyl chloride (AdCl) against LMBV were assessed both in vitro and in vivo . The results showed that AdCl (IC 50  = 72.35 μM) significantly inhibited replication of LMBV in epithelioma papulosum cyprini (EPC) cells. The results of the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide and cytopathic effect (CPE) assays confirmed that AdCl inhibited replication of LMBV in EPC cells and significantly reduced the CPE effect, respectively. As a potential mechanism, AdCl inhibited apoptosis as determined by fluorescence and transmission electron microscopy. The results of flow cytometry showed that the apoptosis rate was decreased by 69 % in the AdCl-treated group as compared to the LMBV-infected group. Additionally, AdCl inhibited viral release. In vivo , the survival rate was 16.2 % higher in the AdCl-treated group as compared to the LMBV-infected group (26.9 % vs. 10.7 %, respectively). Additionally, the results of quantitative reverse transcription polymerase chain reaction (RT-qPCR) showed that AdCl significantly reduced the viral load of the fish liver, spleen, and kidneys at 3, 6, and 9 days postinfection. In addition, RT-qPCR analysis found that AdCl upregulated expression of immune-related genes to suppress replication of LMBV. Collectively, these results confirmed the anti-LMBV activities of AdCl for use in the aquaculture industry.

研究领域: 水产养殖 · 病毒学 · 免疫学
✓ 已验证 DOI PubMed 高影响因子
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ACS Applied Materials & Interfaces · 2021 · IF 9.229

Templated-Assisted Synthesis of Structurally Ordered Intermetallic Pt3Co with Ultralow Loading Supported on 3D Porous Carbon for Oxygen Reduction Reaction

Xiao-Feng Han,Nadia Batool,Wen-Tao Wang,Hao-Tian Teng,Li Zhang,Ruizhi Yang,Jing-Hua Tian

Simple and reliable mass production of platinum-based alloy catalysts with excellent activity and stability is an enormous challenge for the wide commercialization of proton-exchange membrane fuel cells (PEMFC), especially those with ultralow loading of Pt. Herein, an economical, highly durable, and efficient catalyst consisting of structurally ordered intermetallic Pt3Co alloy nanoparticles with ultralow Pt loading (1.4 wt %) supported on hierarchically porous carbon structure (three-dimensional, 3D Pt3Co/C) were synthesized with large-scale production by the NaCl-template-assisted approach. The obtained best sample, 3D Pt3Co/C#1, exhibited mass activities of 11.56 and 0.70 A mgPt–1 for oxygen reduction reactions (ORRs) in alkaline and acidic electrolytes, which are 60.8 and 6.4 times those of commercial Pt/C, respectively. Furthermore, the 3D Pt3Co/C#1 exhibited excellent stability both in acidic and alkaline electrolytes, with almost no decay of the half-wave potential after 5000 potential cycles. This work proposes a new high-yielding, simple, and environmentally friendly method to fabricate excellent Pt-based alloy electrocatalysts with ultralow loading of Pt, which opens up new hopes for the development of PEMFC.

研究领域: 材料科学 · 电化学 · 燃料电池
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

High mass loading CaV4O9 microflowers with amorphous phase transformation as cathode for aqueous zinc-ion battery

Yehong Du,Xinyu Wang,Yan Zhang,Haibang Zhang,Jianzong Man,Kun Liu,Juncai Sun

Rechargeable zinc-ion batteries (ZIBs) have shown significant promise as alternative battery technology due to their environmental benignity and cost-effectiveness. However, the current development of ZIB cathode is still hindered by various challenges such as less-than-ideal capacity, poor cyclic performance, and the typical use of low mass loading during battery evaluation. Here we prepared a nanosheet-assembled compact CaV 4 O 9 microflowers/carbon nanotubes (CaVO/CNTs) composite film via a facile spray printing technique. The resultant CaVO/CNTs composite film possessed extremely short ion diffusion pathways, excellent electrical conductivity, and superior structural stability. At a high mass loading of 50 mg cm −2 , the as-fabricated electrode could attain an areal capacity of 10.5 mAh cm −2 . Furthermore, CaVO/CNTs underwent phase transformation during the initial charging process to form amorphous V 2 O 5 ·nH 2 O, which could provide more active sites for Zn 2+ storage. As a result, CaVO/CNTs electrode was able to deliver 410 mAh g −1 at 0.1 A g −1 , high-rate performance (270 mAh g −1 at 10 A g −1 ), and ultra-long cyclic life of 91% retention after 3000 cycles. Since CaVO/CNTs film possessed good flexibility and excellent electrical conductivity, a flexible soft-packaged ZIB was assembled based on this film, and it was able to exhibit consistent electrochemical properties under various bending states.

研究领域: 材料科学 · 能源存储
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CANADIAN JOURNAL OF CHEMICAL ENGINEERING · 2025 · IF 1.9

Optimizing the CH4/CO2 dry reforming catalysts: Insights from Ni/SBA-16, Ni/KIT-6, and Ni/MCM-41 supported on silica with different mesopore symmetries

Sarmad Soomro,Zhenkun Sun,Dennis Y. Lu,Zhihao Zhou,Lin Li,Lunbo Duan

Catalyst deactivation due to carbon deposition and sintering poses a significant challenge to the efficient dry reforming of CH 4 and CO 2 into syngas, particularly at high Ni loadings. To tackle this difficulty, ordered mesoporous silicas with varied pore symmetries were employed as supports in this study to synthesize the Ni-based catalysts using hydrothermal treatment. The 10% Ni/MCM-41 catalyst exhibited the highest conversion rates for CO 2 (81%) and CH 4 (77%), with favourable H 2 /CO (0.92) ratios indicating efficient syngas production Higher Ni concentrations increase active sites and catalytic performance, they also increase carbon deposition, reducing catalyst durability. At lower Ni loadings (4% Ni), catalysts with a 3D pore structure showed improved activity and stability, effectively reducing carbon deposition. This study demonstrates that optimized mesopore symmetries and Ni loadings can enhance catalyst efficiency and durability for syngas production.

CAS / MDL: 71-36-3
研究领域: 化学工程 · 材料科学
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