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< Page ,Total 71 >
Enhanced water resistance of Pd/3DOM Ce 0.7 Zr 0.3 O 2 catalysts in methane combustion SCIE
期刊论文 | 2024 , 434 | CATALYSIS TODAY
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Abstract :

Three-dimensionally ordered macroporous (3DOM) Ce0.7Zr0.3O2-supported 0.7 Zr 0.3 O 2-supported Pd (xPd/3DOM x Pd/3DOM Ce 0.7 Zr 0.3 O 2 , x = 0.97, 1.49, and 2.10 wt%) catalysts were fabricated using the polymethyl methacrylate (PMMA) microspheretemplating and polyvinyl alcohol (PVA)-protected reduction methods. It was found that the x Pd/3DOM Ce 0.7 Zr 0.3 O 2 samples with surface areas of 31.9-38.2 m2/g 2 /g possessed a high-quality 3DOM architecture, with the Pd nanoparticles (NPs) being uniformly dispersed on the 3DOM Ce 0.7 Zr 0.3 O 2 surface. Among all of the samples, 1.49 Pd/3DOM Ce 0.7 Zr 0.3 O 2 showed the best CH4 4 combustion activity: The T 10% , T 50% , and T 90% (the temperatures at CH4 4 conversions = 10, 50, and 90%) were 269, 330, and 380 degrees C, respectively; specific reaction rate at 260 degrees C was 115.0 x 10-- 6 mol/(gPd Pd s), and turnover frequency at 260 degrees C (TOFPd) Pd ) was 28.8 x 10-- 3 s-1.-1 . The good catalytic performance of 1.49 Pd/3DOM Ce 0.7 Zr 0.3 O 2 was associated with the well-defined 3DOM structure, high Pd NP dispersion, rich adsorbed oxygen species, and strong interaction between Pd NPs and 3DOM Ce 0.7 Zr 0.3 O 2 . Interestingly, the 1.49 Pd/3DOM Ce 0.7 Zr 0.3 O 2 sample also exhibited superior water-tolerant performance. The product analysis results after the in situ introduction of isotopic water demonstrated that the excellent water resistance of 1.49 Pd/3DOM Ce 0.7 Zr 0.3 O 2 was due to the interaction of oxygen and water to form the peroxy hydroxyl species on the sample surface after the water pretreatment, which was beneficial for the combustion of methane.

Keyword :

Supported palladium catalyst Supported palladium catalyst Water resistance Water resistance Ceria-zirconia solid solution Ceria-zirconia solid solution Methane combustion Methane combustion Three-dimensionally ordered macropore Three-dimensionally ordered macropore

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GB/T 7714 Lin, Hongxia , Liu, Yuxi , Deng, Jiguang et al. Enhanced water resistance of Pd/3DOM Ce 0.7 Zr 0.3 O 2 catalysts in methane combustion [J]. | CATALYSIS TODAY , 2024 , 434 .
MLA Lin, Hongxia et al. "Enhanced water resistance of Pd/3DOM Ce 0.7 Zr 0.3 O 2 catalysts in methane combustion" . | CATALYSIS TODAY 434 (2024) .
APA Lin, Hongxia , Liu, Yuxi , Deng, Jiguang , Jing, Lin , Wang, Zhiwei , Wei, Lu et al. Enhanced water resistance of Pd/3DOM Ce 0.7 Zr 0.3 O 2 catalysts in methane combustion . | CATALYSIS TODAY , 2024 , 434 .
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Mesoporous Si-WO 3-supported Pt catalysts with high catalytic performance and excellent water resistance for toluene oxidation SCIE
期刊论文 | 2024 , 432 | CATALYSIS TODAY
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Abstract :

Reducing emissions of volatile organic compounds (VOCs) is an integral part of improving the quality of the atmospheric environment. Catalytic oxidation has become an effective means of treating low and medium concentration VOCs exhausts due to its advantages in terms of removal efficiency, energy saving and environmental protection. Due to the unique inherent properties of supported precious metal catalysts, they show good catalytic efficiency in VOCs emission reduction. In this study, the mesoporous Si-WO 3 support was first synthesized by the P123-assisted sol -gel method, and the x Pt/Si-WO 3 catalysts with the actual loadings ( x = 0.19, 0.48, and 0.81 wt%) of Pt nanoparticles (NPs) were then obtained, physicochemical properties of these materials were characterized using a variety of techniques, and their catalytic activities and water resistance for the oxidation of toluene were evaluated. The results showed that Pt NPs with an average particle size of 2.3-3.3 nm were highly dispersed on the mesoporous Si-WO 3 support, and the 0.81Pt/Si-WO 3 sample exhibited the highest catalytic activity for toluene oxidation at a space velocity of 20,000 mL/(g h) ( T 50% = 167 degrees C and T 90% = 180 degrees C; specific reaction rate at 160 degrees C = 8.54 mu mol/(g Pt s), turnover frequency (TOF Pt ) at 160 degrees C = 1.67 x 10 - 3 s - 1 , and apparent activation energy = 45 kJ/mol). The good catalytic performance of 0.81Pt/Si-WO 3 was associated with its large surface area, well dispersed Pt NPs, high adsorbed oxygen species concentration, large toluene adsorption capacity, and strong interaction between Pt NPs and mesoporous Si-WO 3 . The 0.81Pt/Si-WO 3 sample possessed excellent water resistance, and the introduction of 5 vol% or 10 vol% water vapor to the reaction system enhanced toluene oxidation since part of water vapor participated in the oxidation of toluene. In addition, the toluene oxidation pathway might obey the sequence of (adsorbed toluene + adsorbed oxygen species) -* benzyl alcohol -* (benzoic acid and benzaldehyde) -* maleic anhydride -* (carbon dioxide and water).

Keyword :

Mesoporous structure Mesoporous structure Water resistance Water resistance Si-doped tungsten oxide Si-doped tungsten oxide Toluene oxidation Toluene oxidation Supported platinum catalyst Supported platinum catalyst Volatile organic compound Volatile organic compound

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GB/T 7714 Wang, Xiaoyu , Deng, Jiguang , Liu, Yuxi et al. Mesoporous Si-WO 3-supported Pt catalysts with high catalytic performance and excellent water resistance for toluene oxidation [J]. | CATALYSIS TODAY , 2024 , 432 .
MLA Wang, Xiaoyu et al. "Mesoporous Si-WO 3-supported Pt catalysts with high catalytic performance and excellent water resistance for toluene oxidation" . | CATALYSIS TODAY 432 (2024) .
APA Wang, Xiaoyu , Deng, Jiguang , Liu, Yuxi , Jing, Lin , Wu, Linke , Feng, Ying et al. Mesoporous Si-WO 3-supported Pt catalysts with high catalytic performance and excellent water resistance for toluene oxidation . | CATALYSIS TODAY , 2024 , 432 .
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The influence of crystal facet on the catalytic performance of MOFs-derived NiO with different morphologies for the total oxidation of propane: The defect engineering dominated by solvent regulation effect SCIE
期刊论文 | 2024 , 475 | JOURNAL OF HAZARDOUS MATERIALS
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Crystal facet and defect engineering are crucial for designing heterogeneous catalysts. In this study, different solvents were utilized to generate NiO with distinct shapes (hexagonal layers, rods, and spheres) using nickelbased metal-organic frameworks (MOFs) as precursors. It was shown that the exposed crystal facets of NiO with different morphologies differed from each other. Various characterization techniques and density functional theory (DFT) calculations revealed that hexagonal-layered NiO (NiO-L) possessed excellent low-temperature reducibility and oxygen migration ability. The (111) crystal plane of NiO-L contained more lattice defects and oxygen vacancies, resulting in enhanced propane oxidation due to its highest O 2 adsorption energy. Furthermore, the higher the surface active oxygen species and surface oxygen vacancy concentrations, the lower the C -H activation energy of the NiO catalyst and hence the better the catalytic activity for the oxidation of propane. Consequently, NiO-L exhibited remarkable catalytic activity and good stability for propane oxidation. This study provided a simple strategy for controlling NiO crystal facets, and demonstrated that the oxygen defects could be more easily formed on NiO(111) facets, thus would be beneficial for the activation of C -H bonds in propane. In addition, the results of this work can be extended to the other fields, such as propane oxidation to propene, fuel cells, and photocatalysis.

Keyword :

Solvent regulation effect Solvent regulation effect Oxygen vacancy Oxygen vacancy Nickel oxide Nickel oxide Density functional theory Density functional theory Propane oxidation Propane oxidation Crystal facet engineering Crystal facet engineering

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GB/T 7714 Chai, Qianqian , Li, Chuanqiang , Song, Liyun et al. The influence of crystal facet on the catalytic performance of MOFs-derived NiO with different morphologies for the total oxidation of propane: The defect engineering dominated by solvent regulation effect [J]. | JOURNAL OF HAZARDOUS MATERIALS , 2024 , 475 .
MLA Chai, Qianqian et al. "The influence of crystal facet on the catalytic performance of MOFs-derived NiO with different morphologies for the total oxidation of propane: The defect engineering dominated by solvent regulation effect" . | JOURNAL OF HAZARDOUS MATERIALS 475 (2024) .
APA Chai, Qianqian , Li, Chuanqiang , Song, Liyun , Liu, Cui , Peng, Tao , Lin, Chuanchuan et al. The influence of crystal facet on the catalytic performance of MOFs-derived NiO with different morphologies for the total oxidation of propane: The defect engineering dominated by solvent regulation effect . | JOURNAL OF HAZARDOUS MATERIALS , 2024 , 475 .
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Ultrasonic-assisted synthesis of Ni based-layered double hydroxide doped carbon nanotube and its highly efficient in water oxidation reaction SCIE
期刊论文 | 2023 , 48 (9) , 3429-3439 | INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
WoS CC Cited Count: 4
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Among the developed electrocatalysts, NiCr-layered double hydroxides (NiCr-LDH) are one of the most effective electrocatalytic materials for water oxidation. However, applications of such a kind of materials are practically limited due to their poor electric conductivity. In this work, the single-walled carbon nanotube (SWCNT) was doped to NiCr-LDH, and the LDH-based nanocomposites were synthesized using the one-step ultrasonic-assisted method. Physicochemical properties of the NiCr-LDH/SWCNT composites were characterized by means of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray (EDX) analysis, transmission electron microscopy (TEM), field emission-scanning electron microscopy (FE-SEM), and linear sweep voltammetry (LSV). The NiCr-LDH/SWCNT composites were used as effective nanomaterials for oxygen evolution reaction (OER) at a near neutral medium. The LSV results confirm that the overpotential of the NiCr-LDH/SWCNT-0.006 sample decreased to about 120 mV at pH = 9.5, as compared with that of the NiCr-LDH or NiCr-LDH-SWCNT-0.006 (prepared by the two-step method) sample. The high oxygen evolution activity of NiCr-LDH/SWCNT-0.006 was associated with the co-presence of the homogeneously dispersed NiCr-LDH, good electrochemical activity, and high electrical conductivity. In addition, the as-prepared optimized NiCr-LDH/SWCNT electrocatalyst was highly stable for the OER reaction. (c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

Keyword :

Ni-based-layered double hydroxide Ni-based-layered double hydroxide Ultrasonic method Ultrasonic method Doped carbon nanotube Doped carbon nanotube Water oxidation Water oxidation Electrocatalyst Electrocatalyst

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GB/T 7714 Foruzin, Leila Jafari , Nejati, Kamellia , Dai, Hongxing et al. Ultrasonic-assisted synthesis of Ni based-layered double hydroxide doped carbon nanotube and its highly efficient in water oxidation reaction [J]. | INTERNATIONAL JOURNAL OF HYDROGEN ENERGY , 2023 , 48 (9) : 3429-3439 .
MLA Foruzin, Leila Jafari et al. "Ultrasonic-assisted synthesis of Ni based-layered double hydroxide doped carbon nanotube and its highly efficient in water oxidation reaction" . | INTERNATIONAL JOURNAL OF HYDROGEN ENERGY 48 . 9 (2023) : 3429-3439 .
APA Foruzin, Leila Jafari , Nejati, Kamellia , Dai, Hongxing , Rezvani, Zolfaghar . Ultrasonic-assisted synthesis of Ni based-layered double hydroxide doped carbon nanotube and its highly efficient in water oxidation reaction . | INTERNATIONAL JOURNAL OF HYDROGEN ENERGY , 2023 , 48 (9) , 3429-3439 .
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一种高效催化氧化二氯甲烷的RuO2/Nb2O5/CeO2催化剂及制备方法 incoPat
专利 | 2023-02-21 | CN202310145431.6
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一种高效催化氧化二氯甲烷的RuO2/Nb2O5/CeO2催化剂及制备方法,属于催化化学与环境化学领域。首先制备纳米CeO2;然后将草酸铌铵(C2H2O4·x(NH3)·x(Nb))溶液负载到CeO2纳米催化剂上干燥焙烧得到Nb2O5/CeO2纳米催化剂,将RuCl3水溶液负载到Nb2O5/CeO2纳米催化剂上干燥焙烧得到RuO2/Nb2O5/CeO2催化剂,记为RuNbCe。本发明的催化剂制备工艺简单,合成过程可控,对二氯甲烷表现出良好的催化活性,且抗氯中毒性能强,使用寿命长,在大气污染控制领域具有良好的应用前景。

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GB/T 7714 邓积光 , 郝文成 , 王治伟 et al. 一种高效催化氧化二氯甲烷的RuO2/Nb2O5/CeO2催化剂及制备方法 : CN202310145431.6[P]. | 2023-02-21 .
MLA 邓积光 et al. "一种高效催化氧化二氯甲烷的RuO2/Nb2O5/CeO2催化剂及制备方法" : CN202310145431.6. | 2023-02-21 .
APA 邓积光 , 郝文成 , 王治伟 , 戴洪兴 , 刘雨溪 , 敬林 et al. 一种高效催化氧化二氯甲烷的RuO2/Nb2O5/CeO2催化剂及制备方法 : CN202310145431.6. | 2023-02-21 .
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一种三维有序大孔钴酸镧负载钯铑锰三元金属催化剂及应用 incoPat
专利 | 2023-02-16 | CN202310125406.1
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一种三维有序大孔钴酸镧负载钯铑锰三元金属催化剂及应用,属于功能材料技术领域。制备方法为:在二苄醚中,采用油相还原法,将乙酰丙酮钯、乙酰丙酮铑和十羰基二锰热解还原,形成PdRhMn三元合金,将得到的PdRhMn纳米晶负载到三维有序大孔(3DOM)LaCoO3载体上,随后经过一步高温灼烧过程,得到PdRhMn/3DOM LaCoO3纳米催化剂。本发明所得催化剂制备过程简单,应用于天然气车尾气净化具有优异的氧化还原活性。

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GB/T 7714 刘雨溪 , 田欣荣 , 戴洪兴 et al. 一种三维有序大孔钴酸镧负载钯铑锰三元金属催化剂及应用 : CN202310125406.1[P]. | 2023-02-16 .
MLA 刘雨溪 et al. "一种三维有序大孔钴酸镧负载钯铑锰三元金属催化剂及应用" : CN202310125406.1. | 2023-02-16 .
APA 刘雨溪 , 田欣荣 , 戴洪兴 , 邓积光 . 一种三维有序大孔钴酸镧负载钯铑锰三元金属催化剂及应用 : CN202310125406.1. | 2023-02-16 .
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一种高效光解水制氢的富氮空位Se掺杂型石墨相氮化碳光催化剂 incoPat
专利 | 2023-03-01 | CN202310201804.7
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一种高效光解水制氢的富氮空位Se掺杂型石墨相氮化碳光催化剂,属于催化剂技术领域。通过采用Se辅助的化学气相沉积(CVD)可控制备工艺,成功构建了富氮空位Se掺杂型石墨相氮化碳(VN/Se‑CN)光催化剂。制备过程中,真空密封于石英安瓿瓶中的石墨相氮化碳在Se蒸汽的高温刻蚀反应下,同时实现了Se元素的掺杂以及氮空位的形成。富氮空位Se掺杂型石墨相氮化碳光催化剂展现出了优异的可见光水分解制氢性能(5418μmol h‑1g‑1)。

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GB/T 7714 敬林 , 张启超 , 戴洪兴 et al. 一种高效光解水制氢的富氮空位Se掺杂型石墨相氮化碳光催化剂 : CN202310201804.7[P]. | 2023-03-01 .
MLA 敬林 et al. "一种高效光解水制氢的富氮空位Se掺杂型石墨相氮化碳光催化剂" : CN202310201804.7. | 2023-03-01 .
APA 敬林 , 张启超 , 戴洪兴 , 邓积光 , 刘雨溪 , 隗陆 . 一种高效光解水制氢的富氮空位Se掺杂型石墨相氮化碳光催化剂 : CN202310201804.7. | 2023-03-01 .
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一种用于对多组分VOCs高效净化的贵金属和分子筛组合的串联式催化剂 incoPat
专利 | 2023-04-17 | CN202310409567.3
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一种用于对多组分VOCs高效净化的贵金属和分子筛组合的串联式催化剂,属于催化领域。将制备的PtSn/CeO2和MnOx/HZSM‑5催化剂通过串联的方式组合。制备方法:采用溶剂热法,将乙酰丙酮铂和二水氯化亚锡同时还原,形成PtSn双金属纳米粒子,采用吸附法将其负载到CeO2载体上,将负载后的催化剂先在管式炉中焙烧,形成PtSn/CeO2双金属纳米催化剂,采用浸渍法制备出MnOx/HZSM‑5催化剂。本发明所制备的PtSn/CeO2&MnOx/HZSM‑5纳米催化剂制备过程简单,对甲苯和三氯乙烯的氧化表现出良好的催化活性,在大气污染控制领域具有良好的应用前景。

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GB/T 7714 刘雨溪 , 李泽娅 , 戴洪兴 et al. 一种用于对多组分VOCs高效净化的贵金属和分子筛组合的串联式催化剂 : CN202310409567.3[P]. | 2023-04-17 .
MLA 刘雨溪 et al. "一种用于对多组分VOCs高效净化的贵金属和分子筛组合的串联式催化剂" : CN202310409567.3. | 2023-04-17 .
APA 刘雨溪 , 李泽娅 , 戴洪兴 , 邓积光 . 一种用于对多组分VOCs高效净化的贵金属和分子筛组合的串联式催化剂 : CN202310409567.3. | 2023-04-17 .
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Enhanced moisture resistance and catalytic stability of ethylene oxidation at room temperature by the ultrasmall MnOx cluster/Pt hetero-junction SCIE
期刊论文 | 2023 , 339 | APPLIED CATALYSIS B-ENVIRONMENTAL
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Ethylene elimination can effectively inhibit the rapid aging of fruits and vegetables in storage and transportation. Improving the low-temperature activity, moisture resistance, and stability of Pt based catalysts is a challenge for catalytic oxidation of ethylene which is an effective elimination method. Herein, we constructed ultrasmall MnOx cluster (< 1 nm) on Pt particles via an alloy in situ transformation strategy, which created a large number of MnOx/Pt interfaces. Among all of the samples, 1.89Pt(2.20)Mn/TiO2 showed the highest catalytic activity in the oxidation of ethylene at a space velocity of 20,000 mL/(g h): T-50% = 34 degrees C and T-90% = 43 degrees C, specific reaction rate at 35 degrees C = 33.0 mu m degrees l/(g(Pt) s), and turnover frequency at 35 degrees C = 6.5 x 10(-3) s(-1). In addition, Pt2.20Mn/TiO2 also exhibited better water resistance and stability than Pt/TiO2. The results of XPS, H2O-TPD, C2H4-TPD, in situ DRIFTS, and (H2O)-O-18 isotopic tracing characterization revealed that the MnOx/Pt interfacial sites accelerated desorption of CO2 and enhanced the activation of surface active oxygen species (O-2 to O-2(2-)). Meanwhile, the numerous interfaces provide more active sites for ethylene adsorption and activation, reducing the inhibitory effect of adsorbed water on ethylene adsorption. It was concluded that the prohibited CO2 adsorption, and increased adsorbed oxygen species were responsible for the excellent catalytic performance and good stability of 1.89Pt(2.20)Mn/TiO2, while the more active sites for ethylene adsorption and activation were responsible for the good water resistance of 1.89Pt(2.20)Mn/TiO2.

Keyword :

Water resistance Water resistance Supported noble metal catalyst Supported noble metal catalyst Bimetallic nanoparticle Bimetallic nanoparticle Isotopic trace Isotopic trace Ethylene oxidation Ethylene oxidation

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GB/T 7714 Hou, Zhiquan , Chen, Meiqi , Liu, Yuxi et al. Enhanced moisture resistance and catalytic stability of ethylene oxidation at room temperature by the ultrasmall MnOx cluster/Pt hetero-junction [J]. | APPLIED CATALYSIS B-ENVIRONMENTAL , 2023 , 339 .
MLA Hou, Zhiquan et al. "Enhanced moisture resistance and catalytic stability of ethylene oxidation at room temperature by the ultrasmall MnOx cluster/Pt hetero-junction" . | APPLIED CATALYSIS B-ENVIRONMENTAL 339 (2023) .
APA Hou, Zhiquan , Chen, Meiqi , Liu, Yuxi , Deng, Jiguang , Jing, Lin , Gao, Ruyi et al. Enhanced moisture resistance and catalytic stability of ethylene oxidation at room temperature by the ultrasmall MnOx cluster/Pt hetero-junction . | APPLIED CATALYSIS B-ENVIRONMENTAL , 2023 , 339 .
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Promotional effect of cobalt doping on catalytic performance of cryptomelane-type manganese oxide in toluene oxidation SCIE
期刊论文 | 2023 , 126 , 263-274 | JOURNAL OF ENVIRONMENTAL SCIENCES
WoS CC Cited Count: 8
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The cryptomelane-type manganese oxide (OMS-2)-supported Co (xCo/OMS-2; x = 5, 10, and 15 wt.%) catalysts were prepared via a pre-incorporation route. The as-prepared materials were used as catalysts for catalytic oxidation of toluene (2000 ppmV). Physical and chemical properties of the catalysts were measured using the X-ray diffraction (XRD), Fourier transform infrared spectroscopic (FT-IR), scanning electron microscopic (SEM), X-ray photoelectron spectroscopy (XPS), and hydrogen temperature-programmed reduction (H-2-TPR) techniques. Among all of the catalysts, 10Co/OMS-2 performed the best, with the T90%, specific reaction rate at 245 degrees C, and turnover frequency at 245 degrees C (TOFCo) being 245 degrees C, 1.23 x 10(-3) mol(toluene)/(g(cat).sec), and 11.58 x 10(-3) sec(-1) for toluene oxidation at a space velocity of 60,000 mL/(g.hr), respectively. The excellent catalytic performance of 10Co/OMS-2 were due to more oxygen vacancies, enhanced redox ability and oxygen mobility, and strong synergistic effect between Co species and OMS-2 support. Moreover, in the presence of poisoning gases CO2, SO2 or NH3, the activity of 10Co/OMS-2 decreased for the carbonate, sulfate and ammonia species covered the active sites and oxygen vacancies, respectively. After the activation treatment, the catalytic activity was partly recovered. The good low-temperature reducibility of 10Co/OMS-2 could also facilitate the redox process accompanied by the consecutive electron transfer between the adsorbed O-2 and the cobalt or manganese ions. In the oxidation process of toluene, the benzoic and aldehydic intermediates were first generated, which were further oxidized to the benzoate intermediate that were eventually converted into H2O and CO2. (C) 2022 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.

Keyword :

Volatile organic compound Volatile organic compound Cryptomelane-type manganese oxide Cryptomelane-type manganese oxide Cobalt doping Cobalt doping Toluene oxidation Toluene oxidation

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GB/T 7714 Dong, Ning , Chen, Mengyue , Ye, Qing et al. Promotional effect of cobalt doping on catalytic performance of cryptomelane-type manganese oxide in toluene oxidation [J]. | JOURNAL OF ENVIRONMENTAL SCIENCES , 2023 , 126 : 263-274 .
MLA Dong, Ning et al. "Promotional effect of cobalt doping on catalytic performance of cryptomelane-type manganese oxide in toluene oxidation" . | JOURNAL OF ENVIRONMENTAL SCIENCES 126 (2023) : 263-274 .
APA Dong, Ning , Chen, Mengyue , Ye, Qing , Zhang, Dan , Dai, Hongxing . Promotional effect of cobalt doping on catalytic performance of cryptomelane-type manganese oxide in toluene oxidation . | JOURNAL OF ENVIRONMENTAL SCIENCES , 2023 , 126 , 263-274 .
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