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等离子喷涂超高温热障涂层用纳米结构La2(Zr(0.75)Ce(0.25))2O7球形喂料的研究 被引量:7
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作者 周飞飞 刘敏 +2 位作者 邓春明 张小锋 王铀 《表面技术》 EI CAS CSCD 北大核心 2020年第4期98-103,112,共7页
目的通过纳米粉体造粒技术制备出适合热喷涂超高温用纳米结构La2(Zr(0.75)Ce(0.25))2O7球形喂料,进而采用热喷涂方法制备出纳米结构的热障涂层,以满足下一代热障涂层服役温度需求。方法以化学共沉淀法合成的纳米La2(Zr(0.75)Ce(0.25))2O... 目的通过纳米粉体造粒技术制备出适合热喷涂超高温用纳米结构La2(Zr(0.75)Ce(0.25))2O7球形喂料,进而采用热喷涂方法制备出纳米结构的热障涂层,以满足下一代热障涂层服役温度需求。方法以化学共沉淀法合成的纳米La2(Zr(0.75)Ce(0.25))2O7粉末为原料,通过球磨、喷雾干燥及热处理工艺制备出纳米结构的La2(Zr(0.75)Ce(0.25))2O7喂料,进而采用大气等离子喷涂方法制备出纳米结构La2(Zr(0.75)Ce(0.25))2O7热障涂层。利用扫描电镜(SEM)和透射电镜(TEM)对原始纳米粉体、纳米喂料及喷涂态涂层进行显微形貌和组织结构分析。此外,通过电感耦合等离子体原子发射光谱法(ICP-AES)对制备的纳米喂料进行成分分析。结果制备出的纳米结构La2(Zr(0.75)Ce(0.25))2O7喂料表面光滑、呈球形,成分与化学计量比基本一致。相对于原始纳米粉末,喂料晶粒长大并不显著。喷涂态涂层部分晶粒长大,但仍保留纳米结构。结论成功制备出纳米结构La2(Zr(0.75)Ce(0.25))2O7球形喂料及纳米结构热障涂层,有望作为下一代超高温热障涂层材料。 展开更多
关键词 等离子喷涂 超高温 热障涂层 纳米结构 La2(zr(0.75)ce(0.25))2o7 球形喂料 造粒
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BaTi_(0.75)Zr_(0.25)O_3陶瓷的低温烧结及介电性能研究
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作者 苏魁范 陈缔 +4 位作者 邓湘云 李建保 王春鹏 张国庆 王黎明 《绝缘材料》 CAS 北大核心 2012年第4期34-37,共4页
通过掺入不同含量的B2O3对BaTi0.75Zr0.25O3(BZT)陶瓷进行低温烧结,研究其对介电性能的影响,并采用X射线衍射进行物相分析。结果表明:掺杂B2O3的BZT陶瓷在1 150℃烧结温度下得到的主晶相均为钙钛矿,且不存在明显的杂相。观察试样的表面... 通过掺入不同含量的B2O3对BaTi0.75Zr0.25O3(BZT)陶瓷进行低温烧结,研究其对介电性能的影响,并采用X射线衍射进行物相分析。结果表明:掺杂B2O3的BZT陶瓷在1 150℃烧结温度下得到的主晶相均为钙钛矿,且不存在明显的杂相。观察试样的表面形貌,当B2O3掺杂量为0%~1.5%时,陶瓷晶粒尺寸逐渐变大,而掺杂量为1.5%~2.5%时,晶粒尺寸稍微变小。随着B2O3含量的增加,BZT陶瓷的介电常数降低,介质损耗略微增大。与未掺杂的BZT陶瓷相比,掺杂B2O3的BZT陶瓷的烧结温度下降了300℃,掺杂1.5%B2O3的BZT陶瓷的结构和介电性能较好。 展开更多
关键词 BaTi0.75zr0.25o3 B2o3 低温烧结 介电性能
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ZrO_2对NiO/CeO_2/γ-Al_2O_3复合催化剂结构的影响 被引量:3
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作者 杨修春 卢振光 +1 位作者 康晓春 韦亚南 《无机材料学报》 SCIE EI CAS CSCD 北大核心 2009年第1期187-191,共5页
以Ni(NO3)2.6H2O、Al(NO3)3.9H2O、ZrOCl2.8H2O和Ce(NO3)3.6H2O为原料,采用共沉淀法分别制备了NiO/CeO2/γ-Al2O3和NiO/CeO2-ZrO2/Al2O3催化剂.通过X射线衍射(XRD)、透射电子显微镜(TEM)和近边X射线吸收精细结构(XANES)等方法对催化剂... 以Ni(NO3)2.6H2O、Al(NO3)3.9H2O、ZrOCl2.8H2O和Ce(NO3)3.6H2O为原料,采用共沉淀法分别制备了NiO/CeO2/γ-Al2O3和NiO/CeO2-ZrO2/Al2O3催化剂.通过X射线衍射(XRD)、透射电子显微镜(TEM)和近边X射线吸收精细结构(XANES)等方法对催化剂的组成结构进行表征.结果表明,煅烧温度高于600℃时,NiO/CeO2/γ-Al2O3催化剂中的NiO与γ-Al2O3载体发生作用,形成NiAl2O4尖晶石;而NiO/CeO2-ZrO2/Al2O3催化剂中,NiO能够稳定存在,没有NiAl2O4尖晶石生成,且Al2O3与CeO2和ZrO2作用形成一种新的Zr0.30Ce0.45Al0.25O1.87固溶体. 展开更多
关键词 共沉淀法 NIo NiAl2o4尖晶石 zr0.30ce0.45Al0.25o1.87固溶体
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Improved sulfur-resistant ability on CO oxidation of Pd/Ce_(0.75)Zr_(0.25)O_2 over Pd/CeO_2-TiO_2 and Pd/CeO_2 被引量:2
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作者 沈美庆 林放 +2 位作者 魏光曦 王建强 朱少春 《Journal of Rare Earths》 SCIE EI CAS CSCD 2015年第1期56-61,共6页
The influence of sulfation on Pd/Ce0.75Zr0.25O2, Pd/Ce O2-Ti O2 and Pd/Ce O2 was investigated. Physical structure and chemical properties of different catalysts were characterized by N2 adsorption, X-ray diffraction(... The influence of sulfation on Pd/Ce0.75Zr0.25O2, Pd/Ce O2-Ti O2 and Pd/Ce O2 was investigated. Physical structure and chemical properties of different catalysts were characterized by N2 adsorption, X-ray diffraction(XRD), CO chemisorption, X-ray photoelectron spectroscopy(XPS), Fourier transform infrared spectroscopy(FT-IR) and X-ray fluorescence(XRF). After 10 h SO2 sulfation, it was found that the decrement on CO oxidation catalytic activity was limited on Pd/Ce0.75Zr0.25O2 compared to Pd/Ce O2-Ti O2 and Pd/Ce O2. It demonstrated that Pd/Ce0.75Zr0.25O2 was more sulfur resistant compared to the other two catalysts. After sulfur exposure, catalyst texture was not much influenced as shown by N2 adsorption and XRD, and surface Pd atoms were poisoned indicated by CO chemisorption results. Pd/Ce0.75Zr0.25O2 and Pd/Ce O2-Ti O2 exhibited less sulfur accumulation compared to Pd/Ce O2 in the sulfation process. Furthermore, XPS results clarified that surface sulfur amount, especially surface sulfates amount on the sulfated catalysts was more crucial for the deactivation in sulfur containing environment. 展开更多
关键词 pd/ce0.75zr0.25o2 pd/ceo2-Tio2 diesel oxidation catalyst So2 poison XPS rare earths
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固-固化学法制备Ce_(0.75)Zr_(0.25)O_2氧化物固溶体及其表征 被引量:1
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作者 郑育英 黄慧民 +1 位作者 李军 邓爱华 《分子催化》 EI CAS CSCD 北大核心 2008年第3期249-253,共5页
以碳酸铈、氯氧锆和草酸为原料,采用机械力活化固-固化学法制得前驱物,前驱物经热分解获得了相应的目标产物Ce0.75Zr0.25O2氧化物固溶体.对前驱体进行了热重-差热(TG-DTA)测试,分析了在球磨及煅烧过程中可能发生的化学反应.采用X-射线衍... 以碳酸铈、氯氧锆和草酸为原料,采用机械力活化固-固化学法制得前驱物,前驱物经热分解获得了相应的目标产物Ce0.75Zr0.25O2氧化物固溶体.对前驱体进行了热重-差热(TG-DTA)测试,分析了在球磨及煅烧过程中可能发生的化学反应.采用X-射线衍射(XRD),透射电镜(TEM)和光电子能谱(XPS)等对产物进行了表征,实验结果表明:产物为单一的立方晶系固溶体,没有单独的氧化锆或氧化铈存在,粉体分散性好,呈圆球状,分布均匀,平均粒径为15.8 nm,比表面积达85.4 m2/g.对机械力活化固相化学反应的机制进行了研究. 展开更多
关键词 ce0.75zr0.25o2 固溶体 固相化学反应 机械力
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Hydrothermal stability of MO_x-Ce_(0.75)Zr_(0.25)O_2 catalysts for NO_x reduction by ammonia
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作者 王敏 司知蠢 +2 位作者 陈磊 吴晓东 於俊 《Journal of Rare Earths》 SCIE EI CAS CSCD 2013年第12期1148-1156,共9页
Various acidic components(MOx:phosphate,sulfate,tungstate and niobate) were loaded on Ce0.75 Zr0.25 O2 powders by an impregnation method.The as-prepared catalysts were hydrothermally treated at 760 oC for 48 h in a... Various acidic components(MOx:phosphate,sulfate,tungstate and niobate) were loaded on Ce0.75 Zr0.25 O2 powders by an impregnation method.The as-prepared catalysts were hydrothermally treated at 760 oC for 48 h in air containing 10 vol.% H2 O to obtain the aged catalysts.The catalysts were characterized by X-ray diffraction,Fourier transform infrared spectroscopy,H2 programmed-reduction,NH3 adsorption and deNOx activity measurements.The results showed that,among the catalysts investigated,the phosphated Ce0.75 Zr0.25 O2 catalyst showed the highest hydrothermal stability.The remained high acidity of the phosphated catalyst with moderate redox property helped to maintain the excellent NH3-SCR activity of hydrothermally aged catalyst.Cerium tungstate led to the poor redox property of the tungstated catalyst although the acidity of catalyst was still high.The decomposition of sulfates at temperatures higher than 600 °C restrained the usage of sulfated catalysts in high temperature conditions.The overall dehydration of niobate to niobium oxides led to the low acidity of hydrothermally aged Nb2 O5-Ce0.75 Zr0.25 O2 catalyst. 展开更多
关键词 ce0.75zr0.25o2 NH3-SCR acidic additives hydrothermal stability rare earths
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Effect of PdOx structure properties on catalytic performance of Pd/Ce0.67Zr0.33O2 catalyst for CO,HC and NOx elimination 被引量:4
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作者 Ting Wang Xiaolin Guo +1 位作者 Siyu Lin Renxian Zhou 《Journal of Rare Earths》 SCIE EI CAS CSCD 2019年第7期706-713,共8页
Pd/Ce0.67Zr0.33O2 catalyst was pretreated in different atmosphere respectively, and characterized by CO chemical adsorption, XPS, HR-TEM, H2-TPR, Raman, OSC and in situ DRIFTS to investigate the effect of the structur... Pd/Ce0.67Zr0.33O2 catalyst was pretreated in different atmosphere respectively, and characterized by CO chemical adsorption, XPS, HR-TEM, H2-TPR, Raman, OSC and in situ DRIFTS to investigate the effect of the structure properties of PdOx species on the catalytic performance for CO, HC and NOx elimination. The results show that Pd/CZ catalyst pretreated in air atmosphere has higher oxidation activity of HC due to having high Pd dispersion and strong interaction between PdOx and CZ support. Pd/CZ-H catalyst pretreated in reducing atmosphere exhibits better catalytic performance of NOx elimination because of having relatively big Pd particle size, more Pd species in metallic state and higher concentration of oxygen vacancies. While for the Pd/CZ-RG catalyst pretreated in reactant atmosphere, strong adsorption of HC species on the surface of catalysts would lead to a part of active sites being covered, which inhibits HC and NO conversions. 展开更多
关键词 PRETREATMENT atmosphere Structure properties of pdox species pd/ce0.67zr0.33o2 CATALYST TWCs performance RARE earths
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Steam effects over Pd/Ce_(0.67)Zr_(0.33)O_2-Al_2O_3 three-way catalyst 被引量:3
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作者 王建强 沈美庆 +3 位作者 王军 高继东 马杰 刘双喜 《Journal of Rare Earths》 SCIE EI CAS CSCD 2012年第8期748-752,共5页
Ceria-zirconia-alumina (CZA) solid solution was prepared by sol-gel method in the present study. 0.5 wt.% Pd supported on CZA was prepared by incipient wetness impregnation. The steam effects for CO and C3H8 oxidati... Ceria-zirconia-alumina (CZA) solid solution was prepared by sol-gel method in the present study. 0.5 wt.% Pd supported on CZA was prepared by incipient wetness impregnation. The steam effects for CO and C3H8 oxidation, three-way catalytic activity and stoichiometric window property were studied. The light-off temperature of the CO oxidation reaction shifted to a lower temperature due to the water-gas shift (WGS) reactions. The oxidation of C3H8 was enhanced due to the steam reforming (SR) reactions. The steam promoted the C3H8 oxidation and NO reduction in three-way catalytic reaction. The amplitude of stoichiometric window was amplified by the addition of water to the feed stream. 展开更多
关键词 pd/ce0.67zr0.33o2-Al2o3 three-way catalytic activity water-gas shift steam reforming stoichiometric window rare earths
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不同载体对甲醇分解钯催化剂性能的影响 被引量:4
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作者 赵明 王海容 +3 位作者 蔡黎 朱艺 龚茂初 陈耀强 《稀有金属材料与工程》 SCIE EI CAS CSCD 北大核心 2010年第3期519-522,共4页
用浸渍法制备了Pd/γ-Al2O3和Pd/Ce0.65Zr0.35O22种甲醇分解催化剂。采用XRD,NH3-TPD(NH3-Temperature-Programmed Desorption),XPS及H2-TPR(H2-Temperature-Programmed-Redution)等手段对2种催化剂的结构和性能进行表征,并考察了催化... 用浸渍法制备了Pd/γ-Al2O3和Pd/Ce0.65Zr0.35O22种甲醇分解催化剂。采用XRD,NH3-TPD(NH3-Temperature-Programmed Desorption),XPS及H2-TPR(H2-Temperature-Programmed-Redution)等手段对2种催化剂的结构和性能进行表征,并考察了催化剂上甲醇低温分解的活性。结果表明,Pd/Ce0.65Zr0.35O2催化剂具有较弱的表面酸性及良好的低温还原性能;XPS结果表明2种催化剂中的Pd均以氧化态形式存在,并且Pd在Ce0.65Zr0.35O2固溶体上呈高度分散状态,Pd与Ce间具有较强的相互作用。结合活性考察可知,Pd+的存在有利于甲醇的分解。Pd/Ce0.65Zr0.35O2催化剂具有高的催化活性,220℃时甲醇转化率接近100%。 展开更多
关键词 Γ-AL2o3 ce0.65zr0.35o2 pd催化剂 甲醇分解
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