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Ca and Sr co-doping induced oxygen vacancies in 3DOM La_(2-x)Sr_(x)Ce_(2-y)CayO_(7-δ)catalysts for boosting low-temperature oxidative coupling of methane
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作者 Tongtong Wu Yuechang Wei +5 位作者 Jing Xiong Yitao Yang Zhenpeng Wang Dawei Han Zhen Zhao Jian Liu 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2024年第4期331-344,共14页
It is urgent to develop catalysts with application potential for oxidative coupling of methane(OCM)at relatively lower temperature.Herein,three-dimensional ordered macro porous(3 DOM)La_(2-x)Sr_(x)Ce_(2-y)CayO_(7-δ)(... It is urgent to develop catalysts with application potential for oxidative coupling of methane(OCM)at relatively lower temperature.Herein,three-dimensional ordered macro porous(3 DOM)La_(2-x)Sr_(x)Ce_(2-y)CayO_(7-δ)(A_(2)B_(2)O_(7)-type)catalysts with disordered defective cubic fluorite phased structure were successfully prepared by a colloidal crystal template method.3DOM structure promotes the accessibility of the gaseous reactants(O2and CH4)to the active sites.The co-doping of Ca and Sr ions in La_(2-x)Sr_(x)Ce_(2-y)CayO_(7-δ)catalysts improved the formation of oxygen vacancies,thereby leading to increased density of surface-active oxygen species(O_(2)^(-))for the activation of CH4and the formation of C2products(C2H6and C2H4).3DOM La_(2-x)Sr_(x)Ce_(2-y)CayO_(7-δ)catalysts exhibit high catalytic activity for OCM at low temperature.3DOM La1.7Sr0.3Ce1.7Ca0.3O7-δcatalyst with the highest density of O_(2)^(-)species exhibited the highest catalytic activity for low-temperature OCM,i.e.,its CH4conversion,selectivity and yield of C2products at 650℃are 32.2%,66.1%and 21.3%,respectively.The mechanism was proposed that the increase in surface oxygen vacancies induced by the co-doping of Ca and Sr ions boosts the key step of C-H bond breaking and C-C bond coupling in catalyzing low-temperature OCM.It is meaningful for the development of the low-temperature and high-efficient catalysts for OCM reaction in practical application. 展开更多
关键词 3DOM catalysts Ca ions Sr ions Low-temperature oxidative couplingof methane Oxygen vacancies O_(2)^(-) species
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WO_(3)-TiO_(2)负载的Pt单原子催化剂光热协同催化丙烷和丙烯氧化
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作者 朱锐杰 康磊磊 +8 位作者 李林 潘晓丽 王华 苏杨 李广亿 程鸿魁 李仁贵 刘晓艳 王爱琴 《物理化学学报》 SCIE CAS CSCD 北大核心 2024年第1期26-27,共2页
单原子催化剂(single-atom catalyst,SAC)可以最大化金属原子利用率,并具有独特的电子特性,已经在各种催化反应中进行了广泛的探索。然而,与纳米催化剂相比,贵金属SAC在烃类氧化反应中通常被认为是不活泼的。在本文中,证明了WO_(3)-TiO_... 单原子催化剂(single-atom catalyst,SAC)可以最大化金属原子利用率,并具有独特的电子特性,已经在各种催化反应中进行了广泛的探索。然而,与纳米催化剂相比,贵金属SAC在烃类氧化反应中通常被认为是不活泼的。在本文中,证明了WO_(3)-TiO_(2)负载的Pt SAC(Pt1/WO_(3)-TiO_(2))在光热协同催化氧化C3H8和C3H6这两种典型的挥发性有机化合物(VOCs)中表现出比相应的纳米催化剂(PtNP/WO_(3)-TiO_(2))高得多的活性。研究发现,Pt1/WO_(3)-TiO_(2)和PtNP/WO_(3)-TiO_(2)都可以通过克服氧中毒来提高光热协同催化C3H8氧化的活性。值得注意的是,Pt1/WO_(3)-TiO_(2)的反应速率达到了3792μmol∙gPt−1∙s^(−1),这对C3H8氧化是一个新的突破。更有趣的是,由于C3H6在PtNP/WO_(3)-TiO_(2)上的强吸附导致催化剂C3H6中毒,因此PtNP/WO_(3)-TiO_(2)上的光热协同催化C3H6氧化无法进行。但是,得益于C3H6和Pt单原子之间适中的相互作用,Pt1/WO_(3)-TiO_(2)上的C3H6中毒在光照下可以被克服。因此,Pt1/WO_(3)-TiO_(2)在光热协同催化C3H6氧化中显示出更高的活性。这项工作表明,SAC的优势不仅在于节约贵金属,还在于可以根据其独特的电子特性发现新的催化反应。 展开更多
关键词 单原子催化剂 光热协同催化 氧化反应 氧中毒 丙烯中毒
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Photocatalytic Synthesis of Hydrocarbon Oxygenates from C_2H_6 and CO_2 over Pd-MoO_3/SiO_2 Catalyst 被引量:2
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作者 Xitao Wang Zhong He Shunhe Zhong Xiufen Xiao 《Journal of Natural Gas Chemistry》 EI CAS CSCD 2007年第2期173-178,共6页
Pd-MoO3/SiO2 catalyst has been prepared using the method of incipient wetness impregnation. The photo absorbing behaviors and chemisorbing properties of the catalyst have been characterized by UV-vis spectra and TPD-M... Pd-MoO3/SiO2 catalyst has been prepared using the method of incipient wetness impregnation. The photo absorbing behaviors and chemisorbing properties of the catalyst have been characterized by UV-vis spectra and TPD-MS experiments. The results indicated that metal Pd loaded on MoOa/SiO2 has a significant effect on the photo absorbing performance of MoOa/SiO2, and an obvious blue shift of the absorption edge is produced. Under UV irradiation, the chemisorption state of CO2 undergoes decomposing process to form CO at 481 K, and a two-site adsorption state of ethane can be formed at around 496 K. Photo-oxidation of ethane using carbon dioxide can mainly produce propanal, ethanol and acetaldehyde in the temperature range of 353-423 K. The presence of metal Pd improves the catalytic activity remarkably. 展开更多
关键词 photo-CATALYSIS carbon dioxide ethane hydrocarbon oxygenates Pd-MoOa/SiO2 catalyst
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Conjugated polymerized bimetallic phthalocyanine based electrocatalyst with Fe-N_(4)/Co-N_(4) dual-sites synergistic effect for zinc-air battery
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作者 Shuaifeng Wang Zhongfang Li +5 位作者 Wenjie Duan Peng Sun Jigang Wang Qiang Liu Lei Zhang Yanqiong Zhuang 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2023年第11期41-53,I0002,共14页
The bifunctional oxygen catalyst is essential for zinc-air batteries(ZABs).Here,an efficient bifunctional oxygen catalyst,PPcFeCo/3D-G,is obtained throughπ-πinteraction between the conjugated polymerized iron-cobalt... The bifunctional oxygen catalyst is essential for zinc-air batteries(ZABs).Here,an efficient bifunctional oxygen catalyst,PPcFeCo/3D-G,is obtained throughπ-πinteraction between the conjugated polymerized iron-cobalt phthalocyanine(PPcFeCo)with excellent thermal stability and three-dimensional graphene(3D-G).The bimetallic synergistic effect of PPcFeCo,verified by DFT(Density functional theory)calculation,andπ-πinteractions enhances the catalytic activity and durability of the PPcFeCo/3D-G.Regarding electrochemical performance,the PPcFeCo/3D-G with a high electron transfer number(3.98,@0.768 V vs.RHE)has excellent half-wave potential(E_(1/2)=0.890 V vs.RHE)and exhibits outstanding reversibility(ΔE=0.700 V,ΔE=Ej=10-E_(1/2)).The liquid ZAB(LZAB)employed PPcFeCo/3D-G displays a high power density(222 m W cm^(-2)),a specific capacity(792 m A h g-1),and excellent durability(120 h).This work has guiding significance for the preparation of high-efficiency bifunctional catalysts. 展开更多
关键词 Zn-airbattery Bifunctional oxygen catalysts Polymerized iron-cobalt phthalocyanine Bimetallic synergy π-πinteraction
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Decoloration and mineralization of yeast wastewater by using Ce-Fe/Al_2O_3 as heterogeneous photo-Fenton catalyst 被引量:1
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作者 韦朝海 张亚平 +1 位作者 吴超飞 胡成生 《Journal of Central South University of Technology》 2006年第5期481-485,共5页
Decoloration and mineralization of yeast wastewater were investigated by using Ce-Fe/Al2O3 as a heterogeneous photo-Fenton catalyst in fluidized bed reactor in order to solve the problem of yeast wastewater discharge.... Decoloration and mineralization of yeast wastewater were investigated by using Ce-Fe/Al2O3 as a heterogeneous photo-Fenton catalyst in fluidized bed reactor in order to solve the problem of yeast wastewater discharge. The experimental results were assessed in terms of total organic carbon(TOC) reduction. The operational and reaction conditions affecting the efficiencies of TOC removal such as initial pH value, H2O2 concentration, catalyst loading and UV power were studied. The results show that TOC is reduced from 347.6 mg/L to 10.8 mg/L, color is changed from 500 units to 0 under the conditions as follows: initial pH value 6.0, H2O2 concentration of 1.000 g/L, catalyst loading of 5 g/L, reaction duration of 120 min and reaction temperature of 30 ℃. The irradiated Ce-Fe/Al2O3 catalyst was complexed with 1,10-phenanthroline and then it was subjected to Fourier transform infrared spectroscopy and diffuse reflectance spectroscopy to confirm the formation of Fe(Ⅱ) in the solid state. Heterogeneous photo-Fenton reaction proves to be effective for the treatment of yeast wastewater. 展开更多
关键词 氧化处理 发酵废水 CE-FE/AL2O3 催化剂 矿化作用
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光-Fenton氧化技术研究进展及其处理水中典型新污染物的应用
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作者 张家鑫 马宁 +4 位作者 张辉 谷晶 杨国军 李章良 王华 《中国渔业质量与标准》 2024年第1期41-51,共11页
水产养殖水体中残留的各种难降解有机污染物使水质下降,影响水产品的质量,阻碍水产养殖业的可持续发展。通过将太阳光引入到传统Fenton反应中而构建的光-Fenton氧化技术具有pH响应范围广、自由基产量多、有机污染物矿化程度高等诸多优势... 水产养殖水体中残留的各种难降解有机污染物使水质下降,影响水产品的质量,阻碍水产养殖业的可持续发展。通过将太阳光引入到传统Fenton反应中而构建的光-Fenton氧化技术具有pH响应范围广、自由基产量多、有机污染物矿化程度高等诸多优势,已成为当前水处理领域研究的热点。本研究系统总结了光-Fenton氧化技术的基本原理,分析了光-Fenton氧化体系常见的催化剂类型、影响光-Fenton氧化体系效率的因素以及其在处理水中典型新污染物方面的应用,并指出开发新型催化剂以实现H2O2原位光化学生成和提高催化剂稳定性及可回收性是实现光-Fenton氧化体系工程化应用的关键,为该技术在水产养殖水处理领域的应用提供了理论支撑。 展开更多
关键词 水产养殖水处理 -Fenton技术 催化剂 有机污染物 羟基自由基
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Amino-Functionalized Reduced Graphene-Oxide-Copper (I) Oxide Composite: A Prospective Catalyst for Photo-Reduction of CO2
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作者 Srijita Basumallick 《Graphene》 2016年第2期90-95,共6页
In the present article, an easy synthetic strategy of a novel composite photo-catalyst comprising of amino-functionalized reduced graphene oxide and Cu2O has been proposed. Role of this composite catalyst in photo red... In the present article, an easy synthetic strategy of a novel composite photo-catalyst comprising of amino-functionalized reduced graphene oxide and Cu2O has been proposed. Role of this composite catalyst in photo reduction of CO2 has been analyzed and it is shown that both amino groups and reduced grapheme oxide, participate in enhancing quantum yield of the photo reduction process. 展开更多
关键词 Reduced Graphene Oxide photo-catalyst Cuprous Oxide
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非均相Photo-Fenton反应中负载型光催化剂研究进展 被引量:3
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作者 刘杨先 张军 +2 位作者 盛昌栋 张永春 赵亮 《现代化工》 CAS CSCD 北大核心 2010年第4期26-30,32,共6页
与Fenton、类Fenton、UV/H2O2以及均相Photo-Fenton体系相比,非均相Photo-Fenton反应体系具有反应效率高?有效pH范围宽广以及催化剂可再生利用等优势,是一项极具发展潜力的新型高级氧化工艺。非均相Photo-Fenton反应体系的关键问题是催... 与Fenton、类Fenton、UV/H2O2以及均相Photo-Fenton体系相比,非均相Photo-Fenton反应体系具有反应效率高?有效pH范围宽广以及催化剂可再生利用等优势,是一项极具发展潜力的新型高级氧化工艺。非均相Photo-Fenton反应体系的关键问题是催化剂问题。着重介绍了近几年来有关非均相Photo-Fenton体系中负载型光催化剂的研究发展概况,对目前光催化剂存在的一些问题以及未来发展方向进行了总结与展望。 展开更多
关键词 photo—Fenton 非均相 催化剂 光催化
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非均相Photo-Fenton反应中催化剂及其光催化机理研究进展 被引量:2
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作者 刘杨先 《化学工业与工程技术》 CAS 2010年第5期18-23,共6页
非均相Photo-Fenton反应体系具有反应效率高、有效pH范围宽广以及催化剂可再生利用等优势,是一项极具发展潜力的新型高级氧化工艺。本文简单介绍了近几年来有关非均相Photo-Fenton体系中负载型光催化剂的最新研究成果,主要包括以SiO_2、... 非均相Photo-Fenton反应体系具有反应效率高、有效pH范围宽广以及催化剂可再生利用等优势,是一项极具发展潜力的新型高级氧化工艺。本文简单介绍了近几年来有关非均相Photo-Fenton体系中负载型光催化剂的最新研究成果,主要包括以SiO_2、Al_2O_3、分子筛、碳基材料、黏土材料等无机载体,以及以离子交换树脂和有机纤维材料等有机载体制备的负载型光催化剂,并且在此基础上着重讨论了光催化机理。对目前非均相Photo-Fenton反应存在的一些问题以及未来发展方向作了总结与展望。 展开更多
关键词 photo- Fenton(光-芬顿) 催化剂 反应机理 光催化
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Solar-Driven Hydrogen Peroxide Production Using Polymer-Supported Carbon Dots as Heterogeneous Catalyst 被引量:3
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作者 Satyabrat Gogoi Niranjan Karak 《Nano-Micro Letters》 SCIE EI CAS 2017年第4期30-40,共11页
Safe, sustainable, and green production of hydro gen peroxide is an exciting proposition due to the role of hydrogen peroxide as a green oxidant and energy carrier for fuel cells. The current work reports the developm... Safe, sustainable, and green production of hydro gen peroxide is an exciting proposition due to the role of hydrogen peroxide as a green oxidant and energy carrier for fuel cells. The current work reports the development of carbon dot-impregnated waterborne hyperbranched polyurethane as a heterogeneous photo-catalyst for solar-driven production of hydrogen peroxide. The results reveal that the carbon dots possess a suitable band-gap of 2.98 eV,which facilitates effective splitting of both water and ethanol under solar irradiation. Inclusion of the carbon dots within the eco-friendly polymeric material ensures their catalytic activity and also provides a facile route for easy catalyst separation, especially from a solubilizing medium.The overall process was performed in accordance with the principles of green chemistry using bio-based precursorsand aqueous medium. This work highlights the potential of carbon dots as an effective photo-catalyst. 展开更多
关键词 Carbon dot photo-catalyst Heterogeneous catalyst Hydrogen peroxide
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以消化污泥和硫酸亚铁铵为原料快速制备高效稳定的Photo-Fenton反应催化剂
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作者 廖年华 董滨 +1 位作者 戴翎翎 戴晓虎 《净水技术》 CAS 2016年第2期71-74,101,共5页
厌氧消化因其能将污泥中的有机物转化为沼气而备受关注。然而,经过厌氧消化后的沼渣即消化污泥仍含有高浓度的重金属和其他有害物质,给传统的污泥处理处置带来一系列的困难。该文通过一种简单的合成方法将消化污泥变成稳定高效的非均相... 厌氧消化因其能将污泥中的有机物转化为沼气而备受关注。然而,经过厌氧消化后的沼渣即消化污泥仍含有高浓度的重金属和其他有害物质,给传统的污泥处理处置带来一系列的困难。该文通过一种简单的合成方法将消化污泥变成稳定高效的非均相催化剂。通过对比消化污泥+(NH4)2Fe(SO4)2和单纯消化污泥对RhB(罗丹明B)降解速率的影响,发现人为添加一定量的(NH4)2Fe(SO4)2,可以有效提高RhB的降解速率,使之在10 min后降解率达到80%,20 min内降解率达到95%,从而大大减少降解有机物所需要的时间。 展开更多
关键词 消化污泥 硫酸亚铁铵 重金属 光助芬顿反应 催化剂
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Preparation,characterization and catalytic properties of S_2O_8^(2-)/ZrO_2-CeO_2 solid superacid catalyst 被引量:25
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作者 樊国栋 沈茂 +1 位作者 张昭 贾发瑞 《Journal of Rare Earths》 SCIE EI CAS CSCD 2009年第3期437-442,共6页
A novel solid superacid catalyst S2O8^2-/ZrO2-CeO2 was prepared by a coprecipitation method and characterized by means of XRD FTIR, BET, TEM and DSC/TG analysis methods. The results indicated that incorporation of app... A novel solid superacid catalyst S2O8^2-/ZrO2-CeO2 was prepared by a coprecipitation method and characterized by means of XRD FTIR, BET, TEM and DSC/TG analysis methods. The results indicated that incorporation of appropriate amounts of Ce into the catalyst was beneficial to the formation of sole tetragonal ZrO2 and effectively prevented from the formation of monoclinic ZrO〉 and restrained the loss of sulfated species. XRD revealed the presence of tetragonal Ce0.16Zr0.84O2phase in the case of S2O8^2-/ZrO2-CeO2 calcined above 500 ℃. Catalytic activities of S2O8^2-/ZrO2-CeO2 for the esterification of lactic acid with n-butanol was studied. The results showed that the optimum conditions were as follows: calcination temperature of the catalyst 600 ℃, n(lactic acid):n(n-butyl alcohol)=1.0:3.0, w(S2O8^2-/ZrO2- CeO2)=12.0%, reaction temperature 145 ℃, and reaction time 2 h. The esterification efficiency of lactic acid was about 96.6%. 展开更多
关键词 solid superacid catalyst S2O8^2-/ZrO2-CeO2 n-butyl lactate ESTERIFICATION rare earths
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LaSrNiO_(4-λ) with K_2NiF_4 Strcture──A Highly Active Catalyst for Direct Decomposition of Nitrogen Monoxide 被引量:3
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作者 ZHAO Zhen YANG Xiang-guang and WU Yue(Changchun Institute of Appl. Chem., Chin. Academy of Sciences, Changchun, 130022) 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 1996年第1期81-86,共6页
A series of perovskite-like mixed oxides La2-xSrxMO4±λ(M =Cu, Co,Ni; x=0,1 ) was prepared and characterized using X-ray powder diffraction. The catalytic properties of these catalysts in NO decompositiori were t... A series of perovskite-like mixed oxides La2-xSrxMO4±λ(M =Cu, Co,Ni; x=0,1 ) was prepared and characterized using X-ray powder diffraction. The catalytic properties of these catalysts in NO decompositiori were tested. The results showed that LaSrNiO4-λ with K2NiF4 structure is very active and stable for the decomposition of NO. 展开更多
关键词 LaSrNiO_(4-λ) Highly activie catalyst Decomposition of nitrogen monoxide
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The Microwave Synthesis and Photo-catalytic Activity of SnO_2·TiO_2 Nano-composite
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作者 杨水斌 廖学红 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2005年第3期78-80,共3页
A microwave-assisted heating approach was developed to fabricate SnO2·TiO2 nano-composite in an aqueoas sohaion of sulphuric acid in the presence of SnO2 nano-powder and titanium sulfate. Powder X-ray diffraction... A microwave-assisted heating approach was developed to fabricate SnO2·TiO2 nano-composite in an aqueoas sohaion of sulphuric acid in the presence of SnO2 nano-powder and titanium sulfate. Powder X-ray diffraction ( XRD ) pattern indicates that the products were a composite with both of anatase-type TiO2 and tetrahedrul SnO2. The prnducts were also characterized by transmission electron microscolry ( TEM ), photoluminescence (PL) spectra. The photo-catalytic property of the as-prepared sample has ulso been studied. The result indicates that the as-prepared sample is a good photo-catadyst. 展开更多
关键词 Nano- materials nano- composite photo- catalyst
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Ce_xTi_(1-x)O_2 Mixed Oxides Supported CuO Catalyst for NO Reduction by CO 被引量:1
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作者 楼莉萍 蒋晓原 +3 位作者 陈英旭 吕光烈 周仁贤 郑小明 《Journal of Rare Earths》 SCIE EI CAS CSCD 2003年第3期331-336,共6页
Ce x Ti 1- x O 2 mixed oxides of different mole ratios ( x =0, 0.1, 0.2~0.9, 1.0) were prepared by co precipitation of TiCl 4 with Ce(NO 3) 3 and then loaded with different amounts of CuO. The effe... Ce x Ti 1- x O 2 mixed oxides of different mole ratios ( x =0, 0.1, 0.2~0.9, 1.0) were prepared by co precipitation of TiCl 4 with Ce(NO 3) 3 and then loaded with different amounts of CuO. The effects of CuO on NO+CO reaction were investigated, and the structure and reductive properties of various CuO/Ce x Ti 1- x O 2 were characterized by the methodologies of BET, TPR and XRD. The results show that different Ce/Ti mole ratios and calcination temperatures induce changes of structure and reductive properties of the Ce x Ti 1- x O 2 mixed oxides. When x =0.1~0.5, amorphous CeTi 2O 6 phase mainly forms at 650 ℃ compared to the formation of CeTi 2O 6 which crystallizes at 800 ℃. When x >0.6, some TiO 2 enters the CeO 2 lattice and a CeO 2 TiO 2 solid solution is formed. The activity of 6%CuO/Ce x Ti 1- x O 2 calcined at 650 ℃ is largely affected by the x values, which is the highest when x =0.3, 0.4 and 0.9. The NO conversion reaches 70% at a reaction temperature of 150 ℃. By comparison, the x values have little effect on the activity of 6%CuO/Ce x Ti 1- x O 2 calcined at 800 ℃ . There are strong interactions between CuO and CeTi 2O 6, i.e., formation of the CeTi 2O 6 phase shifts the CuO reduction peak temperature from 380 to 200 ℃, and CuO, in turn, shifts the CeTi 2O 6 reduction peak temperature from 600 to 300 ℃. 展开更多
关键词 catalitic chemistry Ce x Ti 1- x O 2 mixed oxides CuO/Ce x Ti 1- x O 2 catalysts CeTi 2O 6 phase NO+CO reaction activity rare earths
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Photocatalytic Degradation of Organics in Municipal Treated Wastewater in a Re-Circulation Reactor
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作者 Anna Jesil Cheriyan Jyoti Prakash Sarkar +1 位作者 Feroz Sheik Mahad Said Baawain 《Journal of Environmental Protection》 2013年第12期1449-1452,共4页
In this paper, an experimental investigation on the effect of parameters namely concentration, solar radiation intensity and exposure time on the photo oxidation of pollutants in secondary treated municipal wastewater... In this paper, an experimental investigation on the effect of parameters namely concentration, solar radiation intensity and exposure time on the photo oxidation of pollutants in secondary treated municipal wastewater has been presented. TiO2 was used as the photo catalyst and the experiments were carried out in the month of February 2012 in Oman. The reactor was a glass tube constructed with the provision of adding a reflector. The results showed that photo catalytic treatment is very effective for dilute solutions and the presence of reflector enhances the photo degradation. The reduction in Chemical Oxygen Demand (COD) obtained at the experimental conditions of 0.007 m3/hr flow rate, 15°?inclination angle and 1 g·L-1?TiO2 dosage was 18%. The presence of the reflector increased the degradation to 25% at the above experimental conditions. 展开更多
关键词 COD MUNICIPAL WASTEWATER photo catalyst Solar Radiation
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光增强型可充电锌-空气电池双功能催化剂研究进展
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作者 叶笑笑 芦拓 乔锦丽 《上海大学学报(自然科学版)》 CAS CSCD 北大核心 2023年第5期926-945,F0002,共21页
随着全球工业不断发展,对可再生能源加大投入是解决目前化石燃料消耗和环境污染严重等问题的重要举措.光增强型可充电锌-空气电池可充分地将自然界多余的太阳能转化为电能并储存,从而提高能源利用率和光电转换效率,且其供电不受天气变... 随着全球工业不断发展,对可再生能源加大投入是解决目前化石燃料消耗和环境污染严重等问题的重要举措.光增强型可充电锌-空气电池可充分地将自然界多余的太阳能转化为电能并储存,从而提高能源利用率和光电转换效率,且其供电不受天气变化等自然因素的制约.催化剂作为电极的重要组成部分,对锌-空气电池的性能发挥重要作用.首先介绍了光增强型可充电锌-空气电池的工作原理,在此基础上重点就光/电催化剂的制备方法、性能调控以及双功能特性在可充电锌-空气电池中的研究和应用等进行了概述,最后就该领域今后的研究机遇和面临的挑战进行了总结. 展开更多
关键词 光增强型锌-空气电池 光活性双功能催化剂 析氧反应 氧还原反应
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Improvement of Photoactivity of Titanium Oxide by Codoping Sn-Li-F Elements
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作者 Huaixiang Li Yingshuai Lv Lusheng Chen Hao Tian Lei Yu Shanshan Chen 《材料科学与工程(中英文版)》 2010年第6期44-50,共7页
关键词 二氧化钛微粒 光催化活性 掺锡 氟元素 X射线光电子能谱 亚甲基蓝 晶体结构 煅烧温度
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Kinetics Study on Photocatalytic Degradation of Methyl Orange Catalyzed by Sea Urchin-Like Cu2O
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作者 R. J. Gao T. Ding X. J. Duan 《Journal of Materials Science and Chemical Engineering》 2016年第6期35-40,共6页
Sea urchin-like cuprous oxide with hollow glass microsphere as core was prepared using sodium sulfite as the reducing agent and sodium acetate-acetic acid as buffer solution in copper sulfate solution. Methyl orange w... Sea urchin-like cuprous oxide with hollow glass microsphere as core was prepared using sodium sulfite as the reducing agent and sodium acetate-acetic acid as buffer solution in copper sulfate solution. Methyl orange was selected as degradation target for photocatalytic experiments. The photocatalytic activities were investigated by visible spectro- photometer. Photocatalytic kinetics parameters were studied by the Langmuir-Hinshelwood model and Arrhenius formula. It was observed that the sea urchin-like morphology dramatically improved the photocatalytic activity of cuprous oxide. The photo-degradation belongs to the first-order reaction and the maximum degradation rate could reach 94.37%. The activation energy and pre-exponential factor are 41.18 KJ·mol-1 and 1.07 × 106, respectively. After seven times recycling, the sample still showed high photo-catalytic efficiency and stability. 展开更多
关键词 Cuprous Oxide Sea Urchin-Like photo-catalyst Reaction Kinetic Methyl Orange
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Synthesis of 3-(1-Cyclohexenyl)-2-butanone via Environmentally Friendly Catalysts
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作者 ZHAO Zhen-hua 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2003年第3期350-354,共5页
We substituted several environmentally friendly catalysts which included HY and H- β zeolites, various cation-exchanged β zeolites, and solid-supported ferric chloride for conventional catalysts for the synth... We substituted several environmentally friendly catalysts which included HY and H- β zeolites, various cation-exchanged β zeolites, and solid-supported ferric chloride for conventional catalysts for the synthesis of 3-(1-cyclohexenyl)-2-butanone from the reaction of ethylidenecyclohexane with acetic anhydride at room temperature. HY zeolite was found to be the most effective for this reaction, and gave the acylated product in a 72% yield under the conditions of n (ethylidenecyclohexane)/ n (acetic anhydride)/ m (HY zeolite)=1 mmol/10 mmol/0 100 g, reaction temperature 25 ℃ and reaction time 2 h. The used HY zeolite can be recovered, regenerated and gave almost the same yield as the fresh one. The lifetime of the HY zeolite is over 80 h. The effect of different factors on the reaction has also been investigated. 展开更多
关键词 ACYLATION ZEOLITE Environmentally friendly catalyst 3-(1-Cyclohexenyl)-2-butanone Ethylidenecyclohexane Acetic anhydride Synthesis
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