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Nb-Mo-V-TiO_(2)低温脱硝催化剂及其硫酸氢铵分解性能
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作者 柏源 王圣 +1 位作者 孙天宇 轩宇宁 《工业催化》 CAS 2024年第5期33-38,共6页
通过浸渍法制备一系列Nb掺杂V-Mo-Ti催化剂,研究V_(2)O_(5)负载量及Nb掺杂量对催化剂低温脱硝活性的影响,并测试其硫酸氢铵分解性能。采用XRD、N_(2)吸附-脱附、H_(2)-TPR、NH_(3)-TPD、IR等测试手段对催化剂进行表征。结果表明,Nb掺杂... 通过浸渍法制备一系列Nb掺杂V-Mo-Ti催化剂,研究V_(2)O_(5)负载量及Nb掺杂量对催化剂低温脱硝活性的影响,并测试其硫酸氢铵分解性能。采用XRD、N_(2)吸附-脱附、H_(2)-TPR、NH_(3)-TPD、IR等测试手段对催化剂进行表征。结果表明,Nb掺杂促进了V-Mo-Ti的氧化还原性能,提升催化剂的表面酸性,使催化剂具有更加优异的低温脱硝性能;当空速5 000 h^(-1),反应温度180℃时,1.5Nb-6V-3Mo-Ti催化剂的脱硝效率达到100%。同时Nb掺杂提升了催化剂NO氧化能力,促进硫酸氢氨与NO反应的进行,提升催化剂的低温抗水硫中毒性能。 展开更多
关键词 催化剂工程 低温烟气脱硝 Nb掺杂 硫酸氢铵分解 v-Mo-Ti催化剂
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温度对丙烷选择氧化催化剂Mo-V-Te-Ox催化性能的影响分析
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作者 张超超 郑秀慧 《山西化工》 CAS 2024年第2期107-109,共3页
本文采用三氧化钼、水合硫酸氧钒和二氧化锑为主要原料,并添加氧化铈助剂,在不同温度下进行水热合成,并结合微波干燥和常规加热干燥,通过程序升温焙烧活化制备了复合氧化物Mo-V-Te-Ox催化剂。通过自建的气固相微型反应装置和气相色谱的... 本文采用三氧化钼、水合硫酸氧钒和二氧化锑为主要原料,并添加氧化铈助剂,在不同温度下进行水热合成,并结合微波干燥和常规加热干燥,通过程序升温焙烧活化制备了复合氧化物Mo-V-Te-Ox催化剂。通过自建的气固相微型反应装置和气相色谱的联用对催化剂样品进行了活性评价。 展开更多
关键词 Mo-v-Te-Ox催化剂 水热合成 微波加热法 焙烧活化
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NH_3 selective catalytic reduction of NO: A large surface TiO_2 support and its promotion of V_2O_5 dispersion on the prepared catalyst 被引量:3
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作者 刘欣 李俊华 +4 位作者 李想 彭悦 王虎 江晓明 王兰武 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2016年第6期878-887,共10页
A titania support with a large surface area was developed, which has a BET surface area of 380.5 m^2/g, four times that of a traditional titania support. The support was ultrasonically impregnated with 5 wt% vanadia. ... A titania support with a large surface area was developed, which has a BET surface area of 380.5 m^2/g, four times that of a traditional titania support. The support was ultrasonically impregnated with 5 wt% vanadia. A special heat treatment was used in the calcination to maintain the large surface area and high dispersion of vanadium species. This catalyst was compared to a common V2O5-TiO2 catalyst with the same vanadia loading prepared by a traditional method. The new catalyst has a surface area of 117.7 m^2/g, which was 38% higher than the traditional V2O5-TiO2 catalyst. The selective catalytic reduction(SCR) performance demonstrated that the new catalyst had a wider temperature window and better N2 selectivity compared to the traditional one. The NO conversion was 80% from 200 to 450 °C. The temperature window was 100 °C wider than the traditional catalyst. Raman spectra indicated that the vanadium species formed more V-O-V linkages on the catalyst prepared by the traditional method. The amount of V-O-Ti and V=O was larger for the new catalyst. Temperature programmed desorption of NH3, temperature programmed reduction by H2 and X-ray photoelectron spectroscopy results showed that its redox ability and total acidity were enhanced. The results are helpful for developing a more efficient SCR catalyst for the removal of NOx in flue gases. 展开更多
关键词 v2O5-TiO2 catalyst DENITRIFICATION TITANIA Surface area DISPERSIBILITY
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金属卟啉/碳纳米管仿生催化剂的制备及其在Baeyer-Villiger氧化反应中的催化机理
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作者 陈韶云 周贤太 纪红兵 《化工进展》 EI CAS CSCD 北大核心 2023年第3期1332-1340,共9页
利用金属卟啉环(TPP)上π电子与多壁碳纳米管(MWCNTs)上π电子之间的π-π堆积效应,成功制备了4种金属卟啉/多壁碳纳米管催化剂(FeTPPCl-π-π-c-MWCNTs、FeTPPCl-π-π-MWCNTs、SnTPP-π-π-cMWCNTs和SnTPP-π-π-MWCNTs)。实验表明,... 利用金属卟啉环(TPP)上π电子与多壁碳纳米管(MWCNTs)上π电子之间的π-π堆积效应,成功制备了4种金属卟啉/多壁碳纳米管催化剂(FeTPPCl-π-π-c-MWCNTs、FeTPPCl-π-π-MWCNTs、SnTPP-π-π-cMWCNTs和SnTPP-π-π-MWCNTs)。实验表明,所制备产物可用于酮类化合物Baeyer-Villiger(B-V)氧化反应的仿生催化剂。当反应温度为50℃,1,2-二氯乙烷为溶剂,FeTPPCl-π-π-c-MWCNTs为催化剂,环己酮的转化率达到96%,ε-己内酯的收率为96%。另外,所制备的催化剂对于其他酮类化合物的B-V氧化也表现出良好的催化活性。进一步通过原位电子顺磁共振波谱和原位紫外光谱研究了环己酮的B-V氧化的反应历程,发现金属卟啉/碳纳米管仿生催化剂能同时提高自由基和金属卟啉高价活性物种的稳定性,这有利于增强金属卟啉仿生催化酮类化合物的活性。 展开更多
关键词 金属卟啉 多壁碳纳米管 B-v化学反应 催化剂 活化(作用)
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Effect of TiO_2 surface properties on the SCR activity of NOx emission abatement catalyst 被引量:4
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作者 YEDai-qi TIANLiu-qing LIANGHong 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2002年第4期530-535,共6页
NOx emission abatement catalysts V 2O 5 supported on various TiO 2 including anatase, rutile and mixture of both were investigated with various physico\|chemical measurements such as BET, NH\-3\|TPD, NARP, XRD and ... NOx emission abatement catalysts V 2O 5 supported on various TiO 2 including anatase, rutile and mixture of both were investigated with various physico\|chemical measurements such as BET, NH\-3\|TPD, NARP, XRD and so on, and the effect of TiO\-2 surface properties on the SCR(selective catalytic reduction) activity of V\-2O\-5/TiO\-2 catalysts was studied. It was found that the TiO\-2 surface properties had strong affect on the SCR activity of V\-2O\-5/TiO\-2 catalysts. The stronger acidic property resulted in the higher exposure of active sites as well as the higher SCR activity. 展开更多
关键词 NOx SCR(selective catalytic reduction) surface acidity v\-2O\-5/TiO\-2 catalyst
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Performance of V_2O_5-WO_3-MoO_3/TiO_2 Catalyst for Selective Catalytic Reduction of NO_x by NH_3 被引量:9
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作者 高岩 栾涛 +2 位作者 吕涛 程凯 徐宏明 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2013年第1期1-7,共7页
The V/O5-WO3-MoOy'TiO2 honeycomb catalyst was prepared with industrial grade chemicals. The structural and physico-chemical properties were analyzed with X-ray diffraction (XRD), scanning electron micrograph (SEM... The V/O5-WO3-MoOy'TiO2 honeycomb catalyst was prepared with industrial grade chemicals. The structural and physico-chemical properties were analyzed with X-ray diffraction (XRD), scanning electron micrograph (SEM) and mercury porosimetry. The NOx conversion and durability were investigated on a pilot plant test set under the actual operational conditions of a coal fired boiler. The catalyst monolith had good formability with mass per- centage of V : W : Mo : TiO2 : fiber glass = 1 : 4.5 : 4.5 : 72 : 18. Vanadium, tungsten and molybdenum species were highly dispersed on anatase TiO2 without causing the transformation of anatase TiO2 to ruffle by calcining under a current of air at 450℃ for 4.5 h, but there were some degrees of crystal distortion. The catalyst particle sizes were almost uniform with close pile-up and the pore structure was regular with complete macro-pore formation and large specific surface area. The NOx conversion was sensitive to temperature but nearly insensitive to NH3. The catalyst showed strong adaptability to NOx concentration with activity above 80% in the range of 615 1640 mg.m-3. Within the range of 720-8640 h continuous operation, the NOx conversion dropped at a rate of about 1% reduction per 600 h. 展开更多
关键词 selective catalytic reduction v2O5-WO3-MoO3/ZiO2 catalyst physico-chemical property flue gas life time
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Improving the denitration performance and K-poisoning resistance of the V_2O_5-WO_3/TiO_2 catalyst by Ce^(4+) and Zr^(4+) co-doping 被引量:14
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作者 Jun Cao Xiaojiang Yao +4 位作者 Fumo Yang Li Chen Min Fu Changjin Tang Lin Dong 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2019年第1期95-104,共10页
A series of V2O5‐WO3/TiO2‐ZrO2,V2O5‐WO3/TiO2‐CeO2,and V2O5‐WO3/TiO2‐CeO2‐ZrO2 catalysts were synthesized to improve the selective catalytic reduction(SCR)performance and the K‐poisoning resistance of a V2O5‐W... A series of V2O5‐WO3/TiO2‐ZrO2,V2O5‐WO3/TiO2‐CeO2,and V2O5‐WO3/TiO2‐CeO2‐ZrO2 catalysts were synthesized to improve the selective catalytic reduction(SCR)performance and the K‐poisoning resistance of a V2O5‐WO3/TiO2 catalyst.The physicochemical properties were investigated by using XRD,BET,NH3‐TPD,H2‐TPR,and XPS,and the catalytic performance and K‐poisoning resistance were evaluated via a NH3‐SCR model reaction.Ce^4+and Zr^4+co‐doping were found to enhance the conversion of NOx,and exhibit the best K‐poisoning resistance owing to the largest BET‐specific surface area,pore volume,and total acid site concentration,as well as the minimal effects on the surface acidity and redox ability from K poisoning.The V2O5‐WO3/TiO2‐CeO2‐ZrO2 catalyst also presents outstanding H2O+SO2 tolerance.Finally,the in situ DRIFTS reveals that the NH3‐SCR reaction over the V2O5‐WO3/TiO2‐CeO2‐ZrO2 catalyst follows an L‐H mechanism,and that K poisoning does not change the reaction mechanism. 展开更多
关键词 v2O5‐WO3/TiO2‐CeO2‐ZrO2 catalyst Co‐doping K‐poisoning NH3‐SCR Reaction mechanism
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Preparation and Characterization of V-K Catalysts Supported on Porous α-alumina Ceramic Substrate for Diesel Soot Oxidation 被引量:1
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作者 隋丽娜 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2009年第5期810-814,共5页
The V-K catalysts were produced on porous α-alumina substrate by a solution impregnation route and the compositions and catalytic activities for soot oxidation were studied by XRD, TG/DTG, DSC and TPR. According to t... The V-K catalysts were produced on porous α-alumina substrate by a solution impregnation route and the compositions and catalytic activities for soot oxidation were studied by XRD, TG/DTG, DSC and TPR. According to the catalytic activity studies, the catalytic activity of the crystalline phases is in the order: KNO3+KVO3〉K3V5O14+KVO3. The appearance of excessive KHCO3 phase will lead to the deterioration of catalytic activity when the catalysts contain higher KNO3 content. It is also found that when the K∶V molar ratio is higher than 1∶1, the prepared catalysts show a strong CO2 absorption characteristic and this behavior will become gradually significant with the increasing of K∶V molar ratio. Considerable amount of absorbed CO2 are strongly bonded to the crystal lattice with onset desorption temperature of 200 ℃. 展开更多
关键词 v-K catalyst oxidation diesel soot catalytic activity
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Oxidation of propane to acrylic acid and acetic acid over alkaline earth-doped Mo-V-Sb-O_x catalysts 被引量:2
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作者 Chandan S.Chaudhari Shailesh S.Sable +2 位作者 Hanumant Gurav Ashutosh A.Kelkar Vilas H.Rane 《Journal of Natural Gas Chemistry》 EI CAS CSCD 2010年第6期593-599,共7页
Alkaline earth metal (Mg,Ca,Sr and Ba)-doped Mo-V-Sb-O x catalysts,prepared by a dry-up method,have been investigated for their catalytic performance in the oxidation of propane under different reaction conditions.T... Alkaline earth metal (Mg,Ca,Sr and Ba)-doped Mo-V-Sb-O x catalysts,prepared by a dry-up method,have been investigated for their catalytic performance in the oxidation of propane under different reaction conditions.The catalysts have been characterized by N2 adsorption-desorption,temperature-programmed desorption (TPD) of NH3,SEM and XRD.Influence of water vapor on the catalytic performance,particularly on the selectivities to acetic acid and acrylic acid,has also been studied.The selectivity to acrylic acid was improved significantly by the doping of alkaline earth metals to Mo-V-Sb-O x catalysts.The surface acidic sites of the catalyst decreased with the doping of the catalyst with alkaline earth metals,which ultimately was found to be beneficial for obtaining high selectivity to acrylic acid.The catalytic activity and product selectivities were found to be influenced by the reaction temperature,C3H8/O2 ratio and space velocity.A significant improvement in the selectivity to acrylic acid has also been observed by the addition of water vapor in the feed of propane and oxygen in the oxidation of propane. 展开更多
关键词 oxidation of propane surface acidity alkaline earth doped Mo-v-Sb-Ox catalysts acrylic acid acetic acid
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THE PREPARATION CHEMISTRY OF V/MgO CATALYST FOR OXIDATIVE DEHYDROGENATION OF ETHYLBENZENE
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作者 Shu CHEN Biao Hua CHEN +1 位作者 Guo Yin LI Yuan Gen YIN 《Chinese Chemical Letters》 SCIE CAS CSCD 1992年第3期227-230,共4页
The structures and catalytic performances of V_2O_5, Mg_3V_2O_8 and V/MgO catalysts have been correlated by means of XRD, FTIR, TPR and flow micro-reactor tests. The postulation about active site has been made. Based ... The structures and catalytic performances of V_2O_5, Mg_3V_2O_8 and V/MgO catalysts have been correlated by means of XRD, FTIR, TPR and flow micro-reactor tests. The postulation about active site has been made. Based on it, better catalysts have been first prepared via grafting and modification with Sb which are better than that via impregnation. 展开更多
关键词 than THE PREPARATION CHEMISTRY OF v/MgO catalyst FOR OXIDATIvE DEHYDROGENATION OF ETHYLBENZENE TPR MgO
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Obtaining and Reviewing X-ray Diffraction Analysis of the Uranium Catalyst SAPO-U, W, V Based on Natural Zeolite Chankanayskoe Deposits for the Oxidation of S02 to S03
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作者 Aibassov Erkin Zhakenovich Kenzhaliev Bagdaulet Kenzhalievich Tussupbaev Nessipbay KuandykovichI Serikbaeva Gulbarshyn Kuanyshkanovna Bulenov Maxat 《Journal of Chemistry and Chemical Engineering》 2014年第1期97-99,共3页
We first obtained by impregnating the zeolite with salts U, W and V and examined the X-ray uranium catalyst SAPO-U, W, V based on natural zeolite Chankanayskogoe deposits for the oxidation of SO2 to SO3.
关键词 Natural zeolite deposits Chankanayskoe uranium catalyst SAPO-U W v the catalytic oxidation SOz to 803 catalysis.
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The effects of Te on the performance of Mo-V catalysts prepared by hydrothermal synthesis
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作者 Hua Chang Jiang Ling Zeng Bin Long Yin 《Chinese Chemical Letters》 SCIE CAS CSCD 2007年第5期585-587,共3页
Some Mo-V-Te--La catalysts with varied component were prepared by hydrothermal synthesis and dried with microwave method. The component of the catalyst were greatly affected the crystal structure and Raman spectrum. T... Some Mo-V-Te--La catalysts with varied component were prepared by hydrothermal synthesis and dried with microwave method. The component of the catalyst were greatly affected the crystal structure and Raman spectrum. The phase in the catalysts was different when the Mo, V, and Te content varied. When the catalyst containing the same Mo, V content, due to the effect of dopant of Te element (V0.07 Mo0.93)5O14 became the main phase in the catalyst. The catalyst also showed good activity for the reaction of selective oxidation propane to acrolein and acrylic acid. 展开更多
关键词 Mo-v based catalysts Hydrothermal synthesis PROPANE Acrylic acid
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Mo对平板式V-Mo/Ti脱硝催化剂活性及SO_(2)氧化性能的影响 被引量:1
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作者 李金珂 黄力 +4 位作者 纵宇浩 岳彦伟 王虎 高义博 韩沛 《工业催化》 CAS 2023年第5期47-52,共6页
在工业脱硝催化剂生产线上制备不同MoO_(3)含量的V-Mo/Ti脱硝催化剂,通过XRF、XRD、N_(2)吸附-脱附、Raman、H_(2)-TPR、NH_(3)-TPD、SO_(2)-TPD、TG和耐磨强度对催化剂物化性质进行分析。在固定床反应器中考察催化剂的脱硝活性,并研究M... 在工业脱硝催化剂生产线上制备不同MoO_(3)含量的V-Mo/Ti脱硝催化剂,通过XRF、XRD、N_(2)吸附-脱附、Raman、H_(2)-TPR、NH_(3)-TPD、SO_(2)-TPD、TG和耐磨强度对催化剂物化性质进行分析。在固定床反应器中考察催化剂的脱硝活性,并研究MoO_(3)含量对催化剂SO_(2)氧化性能的影响。结果表明,提高催化剂中MoO_(3)含量,对催化剂的晶型、孔结构影响较小,对催化剂单板的机械性能有一定的负面影响。相比V-Mo(3)/Ti催化剂,V-Mo(5)/Ti催化剂的酸性变化不大,还原性能提升,具有更好的脱硝活性。当MoO_(3)含量达到质量分数6.98%时,催化剂的总酸量明显降低,导致脱硝活性下降。提高催化剂中MoO_(3)含量造成脱硝反应过程中副产物N_(2) O生成量的增加,但较高的MoO_(3)含量可以有效减少催化剂对SO_(2)的吸附,减少脱硝反应过程中硫酸氢铵的生成。综合来看,V-Mo(5)/Ti催化剂显示了最佳的反应性能。 展开更多
关键词 催化剂工程 脱硝 v-Mo/Ti催化剂 SO_(2)氧化
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醇盐自模板法构筑碳封装NiFeV基电催化剂用于析氧反应
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作者 马恩辉 刘旭坡 +1 位作者 申涛 王得丽 《电化学(中英文)》 CAS 北大核心 2023年第11期10-18,共9页
发展绿色可持续的水电解制氢技术有利于实现“碳中和”战略目标,而开发高效稳定的析氧反应催化剂对水电解技术至关重要。本研究以NiFeV固态金属醇盐为前驱体,采用醇盐自模板法制备碳封装NiFeV基催化剂。研究结果表明,NiFeV基催化剂呈现... 发展绿色可持续的水电解制氢技术有利于实现“碳中和”战略目标,而开发高效稳定的析氧反应催化剂对水电解技术至关重要。本研究以NiFeV固态金属醇盐为前驱体,采用醇盐自模板法制备碳封装NiFeV基催化剂。研究结果表明,NiFeV基催化剂呈现出均匀的球状结构,用于电解水析氧反应电催化剂时仅需381 mV的过电位即可获得20 mA·cm^(–2)的电流密度。NiFeV基催化剂良好的催化活性和稳定性主要得益于均匀的球状结构,V对电子结构的优化调控以及封装碳层对金属颗粒的保护作用。此工作通过V掺杂和碳封装的策略,为提升析氧催化剂的电催化性能提供了有利借鉴。 展开更多
关键词 析氧催化剂 固态金属醇盐 高温裂解 碳封装 钒掺杂
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Research on K-V-rare Earth Metal Catalysts for Diesel Soot Oxidation
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作者 王永涛 隋丽娜 +1 位作者 kang hongquan yu liyan 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2018年第2期331-337,共7页
Five types of KNO_3-NH_4VO_3-rare earth metal nitrate(K-V-rare earth metal) catalysts supported on a-porous alumina ceramic substrates were prepared by a coating method. All the catalysts were characterized by X-ray... Five types of KNO_3-NH_4VO_3-rare earth metal nitrate(K-V-rare earth metal) catalysts supported on a-porous alumina ceramic substrates were prepared by a coating method. All the catalysts were characterized by X-ray diffraction and thermogravimetry/differential scanning calorimetry. Catalytic activities were evaluated by a soot oxidation reaction using a temperature-programmed reaction system. The experimental results show that the addition of rare earth metal compound could obviously improve the catalytic activities of the K-V-based catalysts. The proper ratio of K-V-rare earth metal catalysts can not only lower the soot onset ignition temperature, but also quicken the soot oxidation rate. The crystalline phases formed by K, V, and rare earth metal are stable. 展开更多
关键词 K-v-rare earth metal catalyst diesel soot catalytic activity
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Cd对V-Mo/Ti脱硝催化剂性能的影响
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作者 黄力 纵宇浩 +4 位作者 李金珂 王虎 刘洋 高义博 韩沛 《锅炉技术》 北大核心 2023年第1期15-20,共6页
为明确燃煤烟气飞灰中Cd元素对V-Mo/Ti脱硝催化剂性能的影响,采用浸渍法,制备V-Mo-Cd/Ti催化剂。采用X射线衍射(XRD)、N_(2)-吸附脱附、H_(2)-程序升温还原(TPR)、X射线光电子能谱(XPS)和NH_(3)-程度升温脱附(TPD)等手段,研究了Cd对催... 为明确燃煤烟气飞灰中Cd元素对V-Mo/Ti脱硝催化剂性能的影响,采用浸渍法,制备V-Mo-Cd/Ti催化剂。采用X射线衍射(XRD)、N_(2)-吸附脱附、H_(2)-程序升温还原(TPR)、X射线光电子能谱(XPS)和NH_(3)-程度升温脱附(TPD)等手段,研究了Cd对催化剂物理化学性能的影响。同时,在固定床微型反应器上考察了不同催化剂的脱硝性能。结果表明:Cd会降低催化剂的比表面积。相比V-Mo/Ti催化剂,V-Mo-Cd/Ti催化剂上的V^(5+)物种减少,V^(5+)/(V^(3+)+V^(4+)+V^(5+))比率降低。此外,Cd还会造成催化剂的O_(α)/(O_(α)+O_(β))比率和表面酸量的降低。因此,V-Mo-Cd/Ti催化剂的脱硝活性低于V-Mo/Ti催化剂。通过将V-Mo/Ti催化剂中MoO_(3)的质量分数由3%提升至5%,可以有效减小Cd对催化剂的负面影响。 展开更多
关键词 脱硝 催化剂 v-Mo/Ti
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丙烷氧化脱氢Ni-V-O催化剂的原位电导 被引量:11
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作者 照日格图 葛庆杰 +3 位作者 李文钊 于春英 贾美林 徐恒泳 《物理化学学报》 SCIE CAS CSCD 北大核心 2000年第9期798-803,共6页
应用原位电导方法测定了Ni-V-O系列催化剂在氧+丙烷→氧→丙烷连续变化气氛下的电导率,确定其导电类型并与其丙烷氧化脱氢制丙烯催化性能相关联.结果表明,p型半导体较n型半导体具有优良的催化氧化脱氢性能;在反应气氛下催化剂的p型半... 应用原位电导方法测定了Ni-V-O系列催化剂在氧+丙烷→氧→丙烷连续变化气氛下的电导率,确定其导电类型并与其丙烷氧化脱氢制丙烯催化性能相关联.结果表明,p型半导体较n型半导体具有优良的催化氧化脱氢性能;在反应气氛下催化剂的p型半导性越大,n型半导性越小,其催化活性越高.这是由于p型半导体空穴导电,而n型半导体则为电子迁移导电,使得表面活性氧物种形成机理不同所致. 展开更多
关键词 丙烷 氧化脱氢 丙烯 电导率 Ni-v-O催化剂
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高电位下PEMFC阴极催化层Pt对碳腐蚀的影响
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作者 刘明俊 周芬 +3 位作者 朱振 黄鹏涛 姚志鹏 潘牧 《电源技术》 CAS 北大核心 2024年第6期1003-1010,共8页
结合非色散红外光谱(NDIR)和电化学表征的方法研究了质子交换膜燃料电池阴极催化层在0.8 V恒电位下,碳腐蚀的变化规律及其对Pt氧化过程的依赖性。研究发现0.8 V恒电位下,Pt会导致碳载体的腐蚀更加剧烈。运行100 h后,Pt/C电极的碳损失质... 结合非色散红外光谱(NDIR)和电化学表征的方法研究了质子交换膜燃料电池阴极催化层在0.8 V恒电位下,碳腐蚀的变化规律及其对Pt氧化过程的依赖性。研究发现0.8 V恒电位下,Pt会导致碳载体的腐蚀更加剧烈。运行100 h后,Pt/C电极的碳损失质量达到8.7%,是纯碳电极的3.5倍。Pt/C电极的碳腐蚀规律可以分为三个阶段,第一阶段呈对数增长,第三阶段呈线性增长,中间存在混合增长区。而Pt氧化物累积量分析表明Pt的氧化呈现出两段对数关系,且中间存在一个过渡区,这解释了碳腐蚀的三段规律。活跃的Pt-OH催化碳腐蚀,并快速转化成PtO_(x)等惰性氧化物,大幅降低对碳腐蚀的促进作用,当Pt-OH含量稳定后,碳腐蚀速率达到稳态。电位阶跃工况下,Pt氧化物增长速度明显降低,碳载体质量损失达到了15.55%,几乎是恒电位工况的2倍,表明控制Pt氧化物累积速度会加速碳载体的腐蚀。 展开更多
关键词 碳载体腐蚀 0.8 v恒电位 PT催化剂 Pt氧化物
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V-P-O催化剂上丙烷氧化制丙烯酸的研究 被引量:12
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作者 王宗祥 刘广舜 +1 位作者 毛国梁 匡洞庭 《石油学报(石油加工)》 EI CAS CSCD 北大核心 1998年第3期21-26,共6页
用V-P-O催化剂,以氧为氧化剂,进行丙烷部分氧化,主要产物为丙烯酸及乙酸。研究结果表明,钒源对催化剂反应性能的影响很大。在不加助剂时,催化剂的适宜P/V原子比为1.10。在C03/O2/H2O=0.72~1.08/... 用V-P-O催化剂,以氧为氧化剂,进行丙烷部分氧化,主要产物为丙烯酸及乙酸。研究结果表明,钒源对催化剂反应性能的影响很大。在不加助剂时,催化剂的适宜P/V原子比为1.10。在C03/O2/H2O=0.72~1.08/35.37/63.73,反应热点温度为693~713K,停留时间为19.1~25.4s时,丙烯酸的最佳单程收率为15%,选择性为32%,相应的丙烷转化率为46%。还对催化剂中添加金属助剂进行了探索。 展开更多
关键词 丙烷 氧化 丙烯酸 v-P-O催化剂
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V-M/TiO_2(M=Cu、Cr、Ce、Mn、Mo)催化燃烧含氯有机废气 被引量:16
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作者 黄海凤 宁星杰 +2 位作者 蒋孝佳 顾蕾 卢晗锋 《中国环境科学》 EI CAS CSCD 北大核心 2014年第9期2179-2185,共7页
以TiO2为载体,采用浸渍法制备V-M/TiO2(M=Cu、Cr、Ce、Mn、Mo)双金属氧化物催化剂,考察其催化燃烧氯苯、二氯甲烷等含氯有机废气(CVOCs)的性能,并通过XRD、BET、H2-TPR和NH3-TPD对催化剂进行了表征.结果表明,V-Mo/TiO2催化剂比表面积最... 以TiO2为载体,采用浸渍法制备V-M/TiO2(M=Cu、Cr、Ce、Mn、Mo)双金属氧化物催化剂,考察其催化燃烧氯苯、二氯甲烷等含氯有机废气(CVOCs)的性能,并通过XRD、BET、H2-TPR和NH3-TPD对催化剂进行了表征.结果表明,V-Mo/TiO2催化剂比表面积最大,催化剂表面活性组分的高分散性和良好的酸性分布使得V-Mo/TiO2能够在260oC将氯苯完全转化为CO2和HCl.而V-Mn/TiO2则具有丰富的活性氧,可显著提高催化剂深度氧化二氯甲烷的能力,在380℃时二氯甲烷即可完全燃烧,并且反应对CO2有着很高的选择性. 展开更多
关键词 含氯有机废气(CvOCs) v-M/TiO2双金属催化剂 催化燃烧
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