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Preparation and mechanical properties of in situ Al_2O_3/Al composites by adding NH_4AlO(OH)HCO_3
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作者 姜澜 崔焱洲 +2 位作者 史玉娟 丁友东 袁芳兰 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2011年第10期2181-2185,共5页
Aluminium matrix composite reinforced by Al2O3 particles was produced by adding NH4AlO(OH)HCO3 into molten aluminum.The mechanical properties and wear behavior of the as-fabricated composites were studied.The result... Aluminium matrix composite reinforced by Al2O3 particles was produced by adding NH4AlO(OH)HCO3 into molten aluminum.The mechanical properties and wear behavior of the as-fabricated composites were studied.The results show that during stirring γ-Al2O3 particles were formed via decomposition reaction of NH4AlO(OH)HCO3,and the distribution of Al2O3 particles is more uniform in the matrix aluminum than directly added Al2O3 into molten aluminum.The density and the hardness values of the as-fabricated composites increase with increasing the particle volume fraction,while the tensile strength of the composites decreases with increasing the volume fraction of the Al2O3 particles.The wear rate of the composites decreases with increasing the volume fraction of the particle and loading.The in situ formed Al2O3/Al composite by adding NH4AlO(OH)HCO3 shows more superior mechanical and wear behaviors than that prepared by directly adding Al2O3 particles. 展开更多
关键词 aluminum matrix composite NH4AlooH)Hco3 A12o3 particles microstructure HARDNESS tensile strength wear behavior
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Catalytic oxidation of benzene over nanostructured porous Co_3O_4-CeO_2 composite catalysts 被引量:10
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作者 Chunyan Ma Zhen Mu Chi He Peng Li Jinjun Li Zhengping Hao 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2011年第12期2078-2086,共9页
Mesostructured Co3O4-CeO2 composite was found to be an effective catalytic material for the complete oxidation of benzene. The Co3O4-CeO2 catalysts with different Co/Ce ratios (mol/mol) were prepared via the nanocas... Mesostructured Co3O4-CeO2 composite was found to be an effective catalytic material for the complete oxidation of benzene. The Co3O4-CeO2 catalysts with different Co/Ce ratios (mol/mol) were prepared via the nanocasting method and the mesostructure was replicated from two-dimensional (2D) hexagonal SBA-15 and three-dimensional (3D) cubic KIT-6 silicas, respectively. All the obtained Co3O4-CeO2 catalysts exhibited the similar symmetry with the parent silicas and well ordered mesostructures. The Co3O4- CeO2 catalysts with 2D mesostructure showed lower catalytic activities than the corresponding 3D materials. The Co3O4-CeO2 catalyst nanocasted from KIT-6 and with the Co/Ce ratio of 16/1 possessed the best catalytic benzene oxidation activity due to larger quantities of surface hydroxyl groups and surface oxygenated species. The mesostructured Co3O4-CeO2 material thus shows great potential as a promising eco-environmental catalyst for benzene effective elimination. 展开更多
关键词 benzene elimination NANoCASTING mesoporous co3o4-ceo2 2D/3D structural Co/Ce ratios
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Co_3O_4/CeO_2CO氧化的原位红外光谱研究 被引量:6
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作者 邵建军 朱锡 +1 位作者 张永坤 王明贵 《燃料化学学报》 EI CAS CSCD 北大核心 2012年第2期229-234,共6页
采用沉淀氧化法制备了Co3O4/CeO2催化剂。分别在干、湿条件下进行了一氧化碳氧化反应研究。运用FT-IR表征手段,在钴铈复合氧化物上进行了CO吸附及CO/O2共吸附研究。结果表明,与纯的Co3O4样品相比,Co3O4/CeO2具有明显的抗湿气能力。Co3O4... 采用沉淀氧化法制备了Co3O4/CeO2催化剂。分别在干、湿条件下进行了一氧化碳氧化反应研究。运用FT-IR表征手段,在钴铈复合氧化物上进行了CO吸附及CO/O2共吸附研究。结果表明,与纯的Co3O4样品相比,Co3O4/CeO2具有明显的抗湿气能力。Co3O4/CeO2催化剂在进行CO氧化时,表面形成了类碳酸盐物种。当环境温度低于453 K时,催化剂上类碳酸盐的生成与形成类碳酸盐物种后受热分解存在着动态平衡。当环境温度高于493 K,催化剂上生成的类碳酸盐物全部受热分解。氧化铈的加入提高了催化剂的抗湿气性能。较小粒径的Co3O4与CeO2产生的强相互作用可使CeO2向Co3O4提供氧,因而间接提供了CO氧化需要的氧。 展开更多
关键词 co3o4/ceo2 Co氧化 FT-IR 吸附
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CeO_2和Co_3O_4助剂对镍基催化剂上CH_4积碳和CO_2消碳性能的影响 被引量:16
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作者 杨咏来 李文钊 徐恒泳 《催化学报》 SCIE CAS CSCD 北大核心 2002年第6期517-520,共4页
采用脉冲微反技术研究了添加CeO2 和Co3 O4助剂对镍基催化剂上CH4积碳和CO2 消碳性能的影响 ,并用BET ,TGA ,XPS及CO2 TPSR等技术对催化剂进行了表征 .结果表明 ,添加CeO2 可以提高活性原子Ni0 中d电子的密度 ;Ni0 原子中d电子密度的... 采用脉冲微反技术研究了添加CeO2 和Co3 O4助剂对镍基催化剂上CH4积碳和CO2 消碳性能的影响 ,并用BET ,TGA ,XPS及CO2 TPSR等技术对催化剂进行了表征 .结果表明 ,添加CeO2 可以提高活性原子Ni0 中d电子的密度 ;Ni0 原子中d电子密度的增加在一定程度上抑制了CH4分子中C H键σ电子向d轨道的迁移 ,降低了CH4裂解积碳性能 ;同时加强了Ni0原子d轨道向CO2 空反键π轨道的电子迁移 ,促进了CO2 分子的活化 ,提高了CO2 的消碳活性 .助剂Co3 O4的添加则促进CH4的裂解积碳 ,抑制了CO2 的消碳 .分析表明 ,活性金属与半导体助剂之间存在的金属 半导体相互作用是影响这种机制的主要因素 . 展开更多
关键词 ceo2 co3o4 CH4 Co2 金属-半导体相互作用 镍基催化剂 氧化铈 氧化钴 积碳 消碳 甲烷 二氧化碳
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磁性纳米ZnFe_(2)O_(4)/Ag_(3)PO_(4)复合材料的合成及光催化降解性能 被引量:3
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作者 颜秀花 房娟 唐兰勤 《环境科学学报》 北大核心 2025年第1期135-142,共8页
磁性纳米复合材料作为一种具有回收再利用特性的新型催化剂,在环境科学领域受到了广泛的关注.本研究用水热法合成了磁性纳米ZnFe_(2)O_(4)/Ag_(3)PO_(4)复合材料.X射线衍射(XRD)、紫外-可见漫反射光谱(UV-vis DRS)和扫描电子显微镜(SEM... 磁性纳米复合材料作为一种具有回收再利用特性的新型催化剂,在环境科学领域受到了广泛的关注.本研究用水热法合成了磁性纳米ZnFe_(2)O_(4)/Ag_(3)PO_(4)复合材料.X射线衍射(XRD)、紫外-可见漫反射光谱(UV-vis DRS)和扫描电子显微镜(SEM)对合成的纳米复合材料进行了表征.同时,研究了ZnFe_(2)O_(4)/Ag_(3)PO_(4)复合材料在可见光下降解亚甲基蓝的催化性能.光催化降解结果表明,复合材料对亚甲基蓝的降解能力受ZnFe_(2)O_(4)与Ag_(3)PO_(4)的物质的量的比影响较大,当ZnFe_(2)O_(4)与Ag_(3)PO_(4)的物质的量的比为0.1∶1时,所得复合材料的光催化活性最高.与纯Ag_(3)PO_(4)相比,ZnFe_(2)O_(4)/Ag_(3)PO_(4)具有优异的结构稳定性和循环利用性能.循环4次后,ZnFe_(2)O_(4)/Ag_(3)PO_(4)的回收率为93.1%,光照60 min对亚甲基蓝的降解率为54.5%,回收率下降了5.1%,亚甲基蓝降解率下降了8.1%,而纯的Ag_(3)PO_(4)样品经过4次循环使用后,回收率下降了50.2%,亚甲基蓝的降解率下降了28.7%,说明ZnFe_(2)O_(4)的加入,提高了复合材料的稳定性和磁回收特性.自由基捕获实验表明空穴(h^(+))和超氧自由基(·O_(2)^(-))是亚甲基蓝降解反应中的主要活性物质. 展开更多
关键词 ZnFe_(2)o_(4)/Ag_(3)Po_(4)复合材料 光催化降解 稳定性 磁性
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CeO_2/Co_3O_4氧载体的制备及其甲烷化学链燃烧性能研究 被引量:6
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作者 黄樊 祝星 +3 位作者 魏永刚 郑敏 王华 李孔斋 《燃料化学学报》 EI CAS CSCD 北大核心 2015年第6期761-768,共8页
制备了系列甲烷化学链燃烧用CeO2/Co3O4复合氧载体,采用XRD、H2-TPR、甲烷程序升温和恒温反应对氧载体进行了表征与评价。研究了不同CeO2的负载量对复合氧载体的结构、氧化还原性、产物选择性的影响。结果表明,氧化铈的添加不仅降低了... 制备了系列甲烷化学链燃烧用CeO2/Co3O4复合氧载体,采用XRD、H2-TPR、甲烷程序升温和恒温反应对氧载体进行了表征与评价。研究了不同CeO2的负载量对复合氧载体的结构、氧化还原性、产物选择性的影响。结果表明,氧化铈的添加不仅降低了氧载体的初始反应温度,还延长了有效反应时间,但铈添加量过高会降低产物CO2选择性,使甲烷向部分氧化进行。CeO2(30%)/Co3O4氧载体在650℃经20次循环后甲烷转化率和CO2选择性均未明显降低,表现出较高的活性和化学链循环稳定性。 展开更多
关键词 化学链燃烧 ceo2/co3o4复合氧载体 甲烷 氧化还原性能
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铈基与钴基Co_3O_4-CeO_2氧载体上甲烷化学链转化特性:产物选择性控制 被引量:17
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作者 曾良鹏 黄樊 +2 位作者 祝星 郑敏 李孔斋 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2017年第1期115-125,共11页
采用水热法制备了Co_3O_4/CeO_2(x)[x为钴铈原子摩尔比n(Co)∶n(Ce)=6∶4~9∶1]和Ce_(1-y)Co_yO_(2-δ)(y=0.1~0.4)2个系列复合氧化物,并表征了材料的物理化学性质,考察了这些氧化物作为氧载体参与甲烷化学链转化(化学链燃烧和化学链部... 采用水热法制备了Co_3O_4/CeO_2(x)[x为钴铈原子摩尔比n(Co)∶n(Ce)=6∶4~9∶1]和Ce_(1-y)Co_yO_(2-δ)(y=0.1~0.4)2个系列复合氧化物,并表征了材料的物理化学性质,考察了这些氧化物作为氧载体参与甲烷化学链转化(化学链燃烧和化学链部分氧化)的反应性能.结果表明,2类复合氧化物的甲烷反应活性均明显优于单一氧化物CeO_2或Co_3O_4,但2类氧载体上的甲烷反应产物的选择性具有明显差异.Ce_(1-y)Co_yO_(2-δ)氧载体形成了Ce-Co-O固溶体,储氧能力明显增强,体相晶格氧迁移速率与甲烷活化速率匹配较好,甲烷反应产物以CO和H_2的合成气为主,有利于甲烷的化学链部分氧化.Co_3O_4/CeO_2(x)氧载体中CeO_2与Co3O4之间的相互作用改善了材料的储氧能力和氧化活性,其与甲烷反应时主要生成CO_2,有利于甲烷化学链燃烧.连续性化学链循环实验表明,2类氧载体均具有较好的再生性能和循环稳定性. 展开更多
关键词 甲烷 co3o4/ceo2(x)氧载体 Ce(1-y)Coyo(2-δ)氧载体 化学链部分氧化 化学链燃烧
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Ce/Co比对Ag/CeO_2-Co_3O_4催化剂低温氧化降解甲醛性能的影响 被引量:3
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作者 唐彤 卫广程 +3 位作者 王慧敏 刘墨 张秋林 宁平 《燃料化学学报》 EI CAS CSCD 北大核心 2019年第5期590-597,共8页
采用共沉淀法制备了一系列具有不同Ce/Co比的Ag/CeO_2-Co_3O_4催化剂,对其在甲醛低温氧化降解中的催化性能进行了研究。结果发现,Ag/CeO_2-Co_3O_4催化剂具有较好的甲醛低温降解活性,而Ce/Co比是影响其催化性能的一个重要因素。XRD、氮... 采用共沉淀法制备了一系列具有不同Ce/Co比的Ag/CeO_2-Co_3O_4催化剂,对其在甲醛低温氧化降解中的催化性能进行了研究。结果发现,Ag/CeO_2-Co_3O_4催化剂具有较好的甲醛低温降解活性,而Ce/Co比是影响其催化性能的一个重要因素。XRD、氮吸附-脱附、Raman光谱、H2-TPR和in-situ DRIFTS等表征结果表明,随着Co含量的增加,Ag/CeO_2-Co_3O_4催化剂的孔体积随之增大,而比表面积减小。CeO_2有利于Ag/CeO_2-Co_3O_4催化剂的氧化还原性能提高,促进氧空位增加,提升Co^(2+)的含量,从而有利于氧分子的活化,促进甲醛降解。同时,in-situ DRIFTS结果表明,甲酸盐物种的分解是甲醛在Ag/CeO_2-Co_3O_4催化剂表面催化氧化降解的速控步骤。 展开更多
关键词 共沉淀法 ceo2-co3o4 甲醛催化氧化 氧空位 甲酸盐
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聚合物辅助成型法制备纳米Co_3O_4/CeO_2催化剂及其对CO低温氧化性能研究 被引量:1
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作者 李文成 王际童 +3 位作者 黄海鸿 乔文明 龙东辉 凌立成 《环境科学学报》 CAS CSCD 北大核心 2016年第1期294-300,共7页
采用聚合物辅助成型法,以乙二胺四乙酸(EDTA)和聚乙烯亚胺(PEI)为配位体制备了Co_3O_4/CeO_2催化剂,对其进行了氮气吸附、XRD、XPS、SEM、TEM、H2-TPR和CO-TPR等表征,并考察了材料的CO低温催化性能.结果表明,采用聚合物辅助成型法能够... 采用聚合物辅助成型法,以乙二胺四乙酸(EDTA)和聚乙烯亚胺(PEI)为配位体制备了Co_3O_4/CeO_2催化剂,对其进行了氮气吸附、XRD、XPS、SEM、TEM、H2-TPR和CO-TPR等表征,并考察了材料的CO低温催化性能.结果表明,采用聚合物辅助成型法能够合成出具有三维空间网络结构的纳米Co_3O_4/CeO_2催化剂,Ce的加入有利于获得具有更小尺寸的Co_3O_4颗粒,并提高Co3+的相对含量,从而有利于CO低温催化性能的提高;Ce/Co的摩尔比为1时,样品具有最佳的CO催化性能,在催化温度为30℃时,可使初始浓度为100 ppm的CO完全转化;同时,纯氧气加热吹扫有利于催化剂的稳定再生.本研究可为CO低温催化剂的制备提供重要参考. 展开更多
关键词 聚合物辅助成型法 co3o4 ceo2 Co低温氧化
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CuO对Co_3O_4-CeO_2催化剂富氢气条件下CO优先氧化性能的影响 被引量:2
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作者 刘子魁 卢小林 白雪 《工业催化》 CAS 2017年第1期25-30,共6页
CO优先氧化方法是去除富氢气CO中最为有效的方法,而且钴铈催化剂又受到重点研究和关注。通过共沉淀法制备不同CuO掺杂量的8Co_3O_4-1CeO_2-c CuO催化剂,使用透射电镜、高分辨透射电镜、X射线粉末衍射、N_2吸附-脱附和程序升温还原以及... CO优先氧化方法是去除富氢气CO中最为有效的方法,而且钴铈催化剂又受到重点研究和关注。通过共沉淀法制备不同CuO掺杂量的8Co_3O_4-1CeO_2-c CuO催化剂,使用透射电镜、高分辨透射电镜、X射线粉末衍射、N_2吸附-脱附和程序升温还原以及比表面积等测试手段对催化剂进行表征,并对其在富氢气条件下CO优先氧化性能进行研究。结果表明,掺杂适量CuO的钴铈催化剂,其催化活性较未添加CuO的催化剂明显提高,其中钴铈铜物质的量比为8∶1∶1的催化剂其CO完全转化温度降低至115℃,同时添加适量CuO的催化剂粒径明显减小,表面分散度改善,增强了Cu-Co-Ce间相互作用,具有较好的催化活性。 展开更多
关键词 催化化学 CUo co3o4-ceo2催化剂 Co优先氧化 富氢气 共沉淀法
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Z型异质结复合薄膜UIO-66-NH_(2)/Ag/Ag_(3)PO_(4)/Ni的可见光催化性能及机理
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作者 赵娣 刘洪燕 +4 位作者 王树军 孙欣语 张紫璇 齐学宇 刘子帆 《材料导报》 北大核心 2025年第8期153-158,共6页
设计和合成高效光催化剂需要实现反应位点的精确调控、光诱导载流子的快速迁移以及可见光的有效吸收。本工作采用恒流电沉积法制备了UIO-66-NH_(2)/Ag/Ag_(3)PO_(4)/Ni复合薄膜。UIO-66-NH_(2)和Ag_(3)PO_(4)的能带结构匹配良好,同时纳... 设计和合成高效光催化剂需要实现反应位点的精确调控、光诱导载流子的快速迁移以及可见光的有效吸收。本工作采用恒流电沉积法制备了UIO-66-NH_(2)/Ag/Ag_(3)PO_(4)/Ni复合薄膜。UIO-66-NH_(2)和Ag_(3)PO_(4)的能带结构匹配良好,同时纳米Ag作为光生载流子分离中心,形成了由Ag_(3)PO_(4)、Ag和UIO-66-NH_(2)组成的Z型异质结光催化体系,有效地分离了光生电子-空穴对,保留了强氧化-还原活性位点,因而UIO-66-NH_(2)/Ag/Ag_(3)PO_(4)/Ni复合薄膜在可见光下表现出优异的光催化性能。此外,光电化学测试结果表明,UIO-66-NH_(2)/Ag/Ag_(3)PO_(4)/Ni复合薄膜具有更高的载流子分离速率和更低的催化还原溶解O_(2)的反应势垒。活性物种实验结果表明,·O_(2)^(-)和空穴(h^(+))在光催化降解中起主要作用,进一步证实了系统的Z型异质结光催化降解机制。 展开更多
关键词 UIo-66-NH_(2)/Ag/Ag_(3)Po_(4)/Ni复合薄膜 Z型异质结 恒流电沉积 可见光 光催化
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Preparation of Z-scheme WO_3(H_2O)_(0.333)/Ag_3PO_4 composites with enhanced photocatalytic activity and durability 被引量:9
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作者 Zhen Li Xia Wang +3 位作者 Jinfeng Zhang Changhao Liang Luhua Lu Kai Dai 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2019年第3期326-334,共9页
Ag3PO4 is widely used in the field of photocatalysis because of its unique activity. However, photocorrosion limits its practical application. Therefore, it is very urgent to find a solution to improve the light corro... Ag3PO4 is widely used in the field of photocatalysis because of its unique activity. However, photocorrosion limits its practical application. Therefore, it is very urgent to find a solution to improve the light corrosion resistance of Ag3PO4. Herein, the Z-scheme WO3(H2O)0.333/Ag3PO4 composites are successfully prepared through microwave hydrothermal and simple stirring. The WO3(H2O)0.333/Ag3PO4 composites are characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and UV-Vis spectroscopy. In the degradation of organic pollutants, WO3(H2O)0.333/Ag3PO4 composites exhibit excellent performance under visible light. This is mainly attributed to the synergy of WO3(H2O)0.333 and Ag3PO4. Especially, the photocatalytic activity of 15%WO3(H2O)0.333/Ag3PO4 is the highest, and the methylene blue can be completely degraded in 4 min. In addition, the stability of the composites is also greatly enhanced. After five cycles of testing, the photocatalytic activity of 15%WO3(H2O)0.333/Ag3PO4 is not obviously decreased. However, the degradation efficiency of Ag3PO4 was only 20.2%. This indicates that adding WO3(H2O)0.333 can significantly improve the photoetching resistance of Ag3PO4. Finally, Z-scheme photocatalytic mechanism is investigated. 展开更多
关键词 Photocatalysis Ag3Po4 Wo3(H2o)0.333 composites Z-scheme
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CeO_2-Co_3O_4 Catalysts for CO Oxidation 被引量:3
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作者 许秀艳 李进军 郝郑平 《Journal of Rare Earths》 SCIE EI CAS CSCD 2006年第2期172-176,共5页
CeO2-Co3O4 catalysts for low-temperature CO oxidation were prepared by a co-precipitation method. In combination with the characterization methods of N2 adsorption/desorption, XRD, temperature-programmed reduction (... CeO2-Co3O4 catalysts for low-temperature CO oxidation were prepared by a co-precipitation method. In combination with the characterization methods of N2 adsorption/desorption, XRD, temperature-programmed reduction (TPR), and FT-IR, the influence of the cerium content on the catalytic performance of CeO2-Co3O4 was investigated. The results indicate that the prepared CeO2-Co3O4 catalysts exhibit a better activity than that of pure CeO2 or pure Co3O4. The catalyst with the Ce/Co atomic ratio 1 : 16 exhibits the best activity, which converts 77% of CO at room temperature and completely oxidizes CO at 45 ℃. 展开更多
关键词 Co oxidation ceo2 co3o4 ceo2-co3o4 catalyst rare earths
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Magnetic composite Fe3O4/CeO2 for adsorption of azo dye 被引量:4
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作者 Shaomin Gao Wenwen Zhang +1 位作者 Huiping Zhou Donghui Chen 《Journal of Rare Earths》 SCIE EI CAS CSCD 2018年第9期986-993,共8页
In this paper,magnetic composite Fe3 O4/CeO2(MC Fe/Ce) was synthesized via CeO2 covered onto the surface of Fe3O4 by sol-precipitation method.The as-synthesized samples were characterized by FE-SEM,XRD,SEM-EDS and F... In this paper,magnetic composite Fe3 O4/CeO2(MC Fe/Ce) was synthesized via CeO2 covered onto the surface of Fe3O4 by sol-precipitation method.The as-synthesized samples were characterized by FE-SEM,XRD,SEM-EDS and FT-IR spectrum.The pseudo-second-order(PSO) kinetic can describe well the adsorption of Acid black 210(AB210) onto the as-obtained MC Fe/Ce of which the adsorption isotherm fits the Langmuir adsorption model better than Freundlich adsorption model.Furthermore,the maximum monolayer adsorption capacity of MC Fe/Ce is about 93 mg/g,which is 6 times more than that of commercial CeO2 for AB210.Moreover,the removal rate of the adsorbates for AB210 is 82.3% after first adsorption and still about 70% the fourth forth adsorption experiments within 120 min,which demonstrates that the obtained MC Fe/Ce has outstanding adsorption capacity and good stability.Additionally,the composite can be easily separated from aqueous solution in a few seconds with an external magnetic field due to its magnetic property,which is vital and has potential for its practical applications. 展开更多
关键词 Magnetic ADSoRPTIoN Fe3o4/ceo2 Sol-precipitation AB 210 Rare earths
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Effect of Al2O3np on the Properties and Microstructure of B4Cp/Al Composites 被引量:4
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作者 LIU Tingting PANG Xiaoxuan +2 位作者 XIAN Yajiang LUO Hao ZHANG Pengcheng 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2020年第3期514-519,共6页
Aluminum-matrix boron carbide (B4Cp/Al) is a kind of neutron absorbing material widely used in nuclear spent fuel storage. In order to improve the tensile property of B4Cp/Al composites, a new type of nano-Al2O3 parti... Aluminum-matrix boron carbide (B4Cp/Al) is a kind of neutron absorbing material widely used in nuclear spent fuel storage. In order to improve the tensile property of B4Cp/Al composites, a new type of nano-Al2O3 particle (Al2O3np) reinforced B4Cp/Al + Al2O3np composites were prepared by powder metallurgy method. The Monte Carlo particle transport program (MCNP) was used to determine the influence of Al2O3np on the thermal neutron absorptivity of composites. The universal material testing machine and scanning electron microscope (SEM) were used to study the mechanical properties, microstructure and fracture morphology of B4Cp/Al composites. The results indicated that the neutron absorption properties of B4Cp/Al composites were not affected by the addition of nano-Al2O3 particles in the range of 1 wt%-15 wt%. The addition of Al2O3np can obviously reduce the grain size of B4Cp/Al matrix metals thus improve the tensile strength of the composites. The addition threshold of Al2O3np is about 2.5 wt%. Both B4Cp and Al2O3np change the fracture characteristics of the composites from toughness to brittleness, and the latter is more important. 展开更多
关键词 B4Cp/Al composites nano-Al2o3 particles PRoPERTIES MICRoSTRUCTURE
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Fabrication of Fine-Grained Si_3N_4-Si_2N_2O Composites by Sintering Amorphous Nano-sized Silicon Nitride Powders 被引量:4
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作者 骆俊廷 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2006年第3期97-99,共3页
Si3N4-Si2N2O composites were fabricated with amorphous nano-sized silicon nitride powders by the liquid phase sintering ( LPS ). The Si2 N2O phase was generated by an in-situ reaction 2 Si3 N4 ( s ) + 1.5 02 ( g... Si3N4-Si2N2O composites were fabricated with amorphous nano-sized silicon nitride powders by the liquid phase sintering ( LPS ). The Si2 N2O phase was generated by an in-situ reaction 2 Si3 N4 ( s ) + 1.5 02 ( g ) = 3 Si2 N2O ( s ) + N2 ( g ) . The content of Si2 N2 O phase up to 60% in the volume was obtained at a sintering temperature of 1 650℃ and reduced when the sintering temperature increased or decreased, indicating the reaction is reversible. The mass loss, relative density and average grain size increased with increasing the sintering temperature. The average grain size was less than 500 nm when the sintering temperature was below 1 700 ℃. The sintering procedure contains a complex crystallization and a phase transition : amorphous silicon nitride→equiaxial α- Si3 N4→ equiaxial β- Si3 N4→ rod- like Si2 N2O→ needle- like β- Si3N4 . Small round-shaped β→ Si3 N4 particles were entrapped in the Si2 N2O grains and a high density of staking faults was situated in the middle of Si2 N2O grains at a sintering temperature of 1 650 ℃. The toughness inereased from 3.5 MPa·m^1/2 at 1 600 ℃ to 7.2 MPa· m^1/2 at 1 800 ℃ . The hardness was as high as 21.5 GPa (Vickers) at 1 600 ℃ . 展开更多
关键词 Si3N4-Si2N2o composite in-situ reaction amorphous nano-sized silicon nitride
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Preparation and characterization of (CeO2)x-(Fe2O3)1-x nanocomposites:reduction kinetics and hydrogen storage 被引量:3
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作者 Shimaa G.Sayed Waleed M.A.El Rouby Ahmed A.Farghali 《Rare Metals》 SCIE EI CAS CSCD 2020年第3期218-229,共12页
A series of nanosized CeO2-Fe2O3 mixed-oxide nanocomposites with different Ce4+/Fe3+molar ratios were successfully prepared by a co-precipitation technique.The surface area increased with Fe2O3 content increasing up t... A series of nanosized CeO2-Fe2O3 mixed-oxide nanocomposites with different Ce4+/Fe3+molar ratios were successfully prepared by a co-precipitation technique.The surface area increased with Fe2O3 content increasing up to 60 wt%in the composite.However,with further increase in Fe2O3 content,the surface area began to decrease.The reduction processes of the CeO2-Fe2O3 nanocomposites were studied in a hydrogen atmosphere at 300-600℃.The reduction rates increased by increasing both the temperature and Fe2O3 content in the nanocomposites.The microstructure of the reduced composites at 500℃illustrated the presence of a considerable number of macro-and micro-pores.The activation energy values were calculated which were in the range of 3.56-5.37 kJ mol-1 at the initial stages(up to 35%reduction)and 5.21-10.2 kJ·mol-1 at the final stages(up to 80%reduction)of reduction.The rate-controlling mechanisms in both the initial and final reduction stages were determined,and the initial reaction stage was controlled by combined gaseous diffusion and interfacial chemical reaction mechanisms for all the composites except for pure CeO2,which was controlled by a chemical reaction mechanism.The final reaction stage was controlled by a gaseous diffusion mechanism for some composites,while for the others it was controlled by combined gaseous diffusion and interfacial chemical reaction mechanisms.The hydrogen sorption properties of the nanocomposites were studied by pressure composition isotherms using a volumetric method.Hydrogen storage in the nanocomposites increased by increasing the temperature because of the formation of oxygen vacancies which enhance atomic H adsorption and function as strong adsorption sites forming more metal hydride covalent bonds. 展开更多
关键词 ceo2-Fe2o3 nanocomposite REDUCTIoN kinetics REDUCTIoN mechanism Hydrogen storage oxygen VACANCIES
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Enhanced Photocatalytic Denitrification Rhodamine Bover In2O3/Bi24O31Br10 Nanocomposites under Visible Light Irradiation 被引量:3
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作者 黄继涛 崔春娜 +1 位作者 颜桂炀 邢永雷 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2018年第4期611-616,共6页
A novel In203/Bi24O31Br10 composite photocatalyst, where In2O3 nanoparticleswith the diameter of about 5-10 nm were tightly attached on the surface of Bi24O31Br10 plates, wasprepared by using hydrolysis, impregnation ... A novel In203/Bi24O31Br10 composite photocatalyst, where In2O3 nanoparticleswith the diameter of about 5-10 nm were tightly attached on the surface of Bi24O31Br10 plates, wasprepared by using hydrolysis, impregnation method and post-thermal process. Photocatalyticactivity was evaluated by the degradation of Rhodamine B under the visible light irradiation.Effects of the contents of In203 nanoparticles on the optical property and photocatalytic activity of In203/Bi24O31Br10 composite were also investigated. Compared with neat In203 and Bi24O31Brlomaterials, 15In203/Bi24O31Br10 composite exhibits the best photocatalytic activity owing to theefficient separation of photogenerated electron and hole pairs, which is evidenced byphotoluminence spectra. More than 95% of Rhodamine B solution can be degraded by15In203/Bi24O31Brlo sample in 30 min. 展开更多
关键词 PHoToCATALYST In2o3/Bi24o31Br10 composite photocatalytic activity rhodamine B
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水蒸汽对Ni/CeO_2-ZrO_2-Al_2O_3催化剂上CO_2+CH_4重整反应的影响 被引量:11
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作者 李春林 伏义路 +4 位作者 孟明 卞国柱 谢亚宁 胡天斗 张静 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 北大核心 2004年第1期95-99,共5页
用水热合成法制备了Ni/CeO2 ZrO2 Al2 O3 催化剂 .进行了添加和不添加水蒸汽的CH4 +CO2 催化重整反应 ,测试了活性和稳定性 ,测量了积碳量 ,并用XAFS手段测试了催化剂Ni的K吸收边 .结果表明 ,在反应过程中有CeAlO3 的生成 ,但积碳是... 用水热合成法制备了Ni/CeO2 ZrO2 Al2 O3 催化剂 .进行了添加和不添加水蒸汽的CH4 +CO2 催化重整反应 ,测试了活性和稳定性 ,测量了积碳量 ,并用XAFS手段测试了催化剂Ni的K吸收边 .结果表明 ,在反应过程中有CeAlO3 的生成 ,但积碳是无水蒸汽添加的反应活性降低的原因 .反应气中添加水蒸汽能够减少积碳 ,从而提高催化反应的稳定性 .由于碳原子插入Ni晶格 ,无水蒸汽反应后的最近邻Ni Ni配位数有较大幅度的减少 .添加了水蒸汽的反应 ,最近邻Ni Ni配位数比反应前减少幅度小 ,这主要是由于在反应气中添加水蒸汽减少了积碳 。 展开更多
关键词 Co2+CH4重整反应 添加水蒸汽 Ni/ceo2-Zro2-Al2o3催化剂 XAFS 积碳
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Ni/CeO_2-Al_2O_3催化剂上CH_4-CO_2转化积炭性能的研究 被引量:21
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作者 杨咏来 徐恒泳 李文钊 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2002年第11期2112-2116,共5页
采用脉冲微量反应技术研究了添加 n型半导体氧化物 Ce O2 对 Ni基催化剂上 CH4积炭 /CO2 消炭性能的影响 ,用 TPR,XPS和氢吸附技术对催化剂进行了表征 .结果表明 ,活性金属原子 Ni与半导体氧化物Ce O2 之间存在金属 -半导体相互作用 ( M... 采用脉冲微量反应技术研究了添加 n型半导体氧化物 Ce O2 对 Ni基催化剂上 CH4积炭 /CO2 消炭性能的影响 ,用 TPR,XPS和氢吸附技术对催化剂进行了表征 .结果表明 ,活性金属原子 Ni与半导体氧化物Ce O2 之间存在金属 -半导体相互作用 ( MSc I) ,Ce O2 的添加提高了活性原子 Ni0的 d电子密度 ,在一定程度上抑制了 CH4分子中 C—Hσ电子向 d轨道的迁移 ,降低了 CH4裂解积炭活性 ;可加强 Ni0原子 d轨道向CO2 空反键 π轨道的电子迁移 ,促进 CO2 分子的活化 ,提高 CO2 的消炭活性 ,使 Ni/Ce O2 -Al2 O3 催化剂具有较强的抗积炭性能 . 展开更多
关键词 Ni/ceo2-Al2o3催化剂 金属-半导体相互作用 金属-载体相互作用 CH4 积炭 Co2 消炭 氧化铈 氧化铝 载体 合成气 甲烷 二氧化碳
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