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磁性CeO_2-Fe_3O_4复合材料光催化/吸附去除水中As(Ⅲ) 被引量:8
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作者 孙天一 赵志伟 +1 位作者 时文歆 崔福义 《环境科学学报》 CAS CSCD 北大核心 2018年第8期3108-3117,共10页
原水砷污染问题严重威胁饮用水水质安全,随着生活饮用水标准的提高,致使多地饮用水中砷超标问题突显.本研究利用CeO_2半导体的光催化活性及CeO_2和Fe_3O_4对As(Ⅴ)的强亲和力,合成了双组份磁性CeO_2-Fe_3O_4复合材料,并采用SEM、XRD、BE... 原水砷污染问题严重威胁饮用水水质安全,随着生活饮用水标准的提高,致使多地饮用水中砷超标问题突显.本研究利用CeO_2半导体的光催化活性及CeO_2和Fe_3O_4对As(Ⅴ)的强亲和力,合成了双组份磁性CeO_2-Fe_3O_4复合材料,并采用SEM、XRD、BET和VSM等手段进行表征,考察复合材料的光催化/吸附除砷效果;研究了初始p H值、共存离子等因素对吸附除砷效果的影响;采用等温吸附模型、吸附动力学模型等手段进行吸附特性研究.实验结果表明,在光催化过程中,·OH和·O_2^-为主要的活性氧化物种.在紫外照射下,As(Ⅲ)能完全被氧化为毒性较低的As(Ⅴ),同时将As(Ⅴ)高效吸附于CeO_2-Fe_3O_4粒子表面.在中性条件下,CeO_2-Fe_3O_4粒子对砷的饱和吸附量为122.19 mg·g^(-1).共存离子Cl^-和SO_4^(2-)对As(Ⅴ)的吸附没有显著影响,而CO_3^(2-)、SiO_3^(2-)和PO_4^(3-)与As(Ⅴ)存在明显的竞争吸附,使As(Ⅴ)的吸附去除效果明显降低.吸附动力学和吸附等温线模拟分别符合准二级动力学方程和Freundlich吸附等温线,表明As(Ⅴ)的吸附以化学吸附为主导.CeO_2-Fe_3O_4复合吸附剂可快速实现固液分离,容易再生且重复利用性较好,具有广泛的应用前景. 展开更多
关键词 ceo2-fe3o4复合材料 光催化 吸附 As(Ⅲ) As(Ⅴ) 磁性
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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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Properties of Hot-Pressed Al_2O_3-Fe Composites 被引量:4
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作者 M.M.El-Sayed Seleman, Xudong SUN and Liang ZUO Department of Materials Science and Engineering, Northeastern University, Shenyang 110006, China K.A.Khalil Powder Metallurgy Institute, Central South University, Changsha 410083, China 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2001年第5期538-542,共5页
Alumina-(0 similar to 20 vol. pct) iron composites were fabricated by hot-pressing of well-mixed-alumina and iron powders at 1400 degreesC and 30 MPa for 30 min. Hot-pressed bodies with nearly theoretical density were... Alumina-(0 similar to 20 vol. pct) iron composites were fabricated by hot-pressing of well-mixed-alumina and iron powders at 1400 degreesC and 30 MPa for 30 min. Hot-pressed bodies with nearly theoretical density were obtained for addition up to 10 vol. pct Fe, but relative density decreased gradually with further increase in Fe addition. The materials exhibit a homogeneous dispersion of Fe. Fracture strength of the composites exhibits a maximum value of 604 MPa at 15 vol. pct Fe, which is 1.5 times that of alumina alone. Fracture toughness increases with the increase in Fe content, reaching 7.5 MPa.m(1/2) at 20 vol. pct Fe. The theoretical values of fracture toughness was calculated and compared with the experimental one. Toughening mechanisms of the composites are also discussed. 展开更多
关键词 FE Properties of Hot-Pressed Al2o3-fe composites AL
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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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Preparation and characterization of (CeO2)x-(Fe2O3)1-x nanocomposites:reduction kinetics and hydrogen storage 被引量:2
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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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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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Na_(2)CO_(3)·10H_(2)O-Na_(2)HPO_(4)·12H_(2)O/SiO_(2)复合定形相变材料的制备及应用 被引量:5
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作者 王璇 李再超 +2 位作者 吴亚楠 唐炳涛 张宇昂 《精细化工》 EI CAS CSCD 北大核心 2024年第3期623-629,656,共8页
以Na_(2)CO_(3)·10H_(2)O(SCD)、Na_(2)HPO_(4)·12H_(2)O(DHPD)为相变主体制备了共晶体系,通过绘制凝固点变化图与DSC测试共同确定在m(SCD)∶m(DHPD)=4∶6时形成共晶,FTIR和XRD结果显示,2种水合盐间没有发生化学反应,但其晶... 以Na_(2)CO_(3)·10H_(2)O(SCD)、Na_(2)HPO_(4)·12H_(2)O(DHPD)为相变主体制备了共晶体系,通过绘制凝固点变化图与DSC测试共同确定在m(SCD)∶m(DHPD)=4∶6时形成共晶,FTIR和XRD结果显示,2种水合盐间没有发生化学反应,但其晶型结构发生改变。通过添加质量分数为2%的Na2SiO3·9H_(2)O作为成核剂降低体系的过冷度,且经历50次相变循环体系未出现相分离,相变焓值仅下降0.25%。进一步使用质量分数为25%的气相SiO_(2)作为支撑材料,采用浸渍法制备了相变前后形状稳定的共晶水合盐/SiO_(2)定形相变材料(SSPCM)。所得SSPCM的相变温度为24.08℃,相变焓值为146.6J/g,过冷度为0.55℃,热导率为0.4571W/(m·K)。同保温泡沫相比,其可将模拟房内部中心温度的升温时间延长了1.81倍,降温时间延长了0.39倍。 展开更多
关键词 Na_(2)Co_(3)·10H_(2)o Na_(2)HPo_(4)·12H_(2)o 共晶水合盐 复合相变材料 建筑节能 功能材料
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Synthesis of Y_2O_3 particle enhanced Ni/TiC composite on TC4 Ti alloy by laser cladding 被引量:19
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作者 张可敏 邹建新 +2 位作者 李军 于治水 王慧萍 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2012年第8期1817-1823,共7页
A Y2O3 particle enhanced Ni/TiC composite coating was fabricated in-situ on a TC4 Ti alloy by laser surface cladding. The phase component, microstructure, composition distribution and properties of the composite layer... A Y2O3 particle enhanced Ni/TiC composite coating was fabricated in-situ on a TC4 Ti alloy by laser surface cladding. The phase component, microstructure, composition distribution and properties of the composite layer were investigated. The composite layer has graded microstructures and compositions, due to the fast melting followed by rapid solidification and cooling during laser cladding. The TiC powders are completely dissolved into the melted layer during melting and segregated as fine dendrites when solidified. The size of TiC dendrites decreases with increasing depth. Y2O3 fine particles distribute in the whole clad layer. The Y2O3 particle enhanced Ni/TiC composite layer has a quite uniform hardness along depth with a maximum value of HV1380, which is 4 times higher than the initial hardness. The wear resistance of the Ti alloy is significantly improved after laser cladding due to the high hardness of the composite coating. 展开更多
关键词 TC4 Ti alloy Ni/TiC composite Y2o3 laser cladding HARDNESS surface modification
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Effects of CeO_2 additives on the microstructure and mechanical properties of WC-Al_2O_3 composites 被引量:1
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作者 QU Haixia WU Qiong WEN Hongquan 《Baosteel Technical Research》 CAS 2015年第3期17-22,共6页
To improve the mechanical properties of WC-Al2O3 composites, the effects of trace amount of CeO2 additives on the microstructure and mechanical properties of the WC-Al2O3 composites prepared by hot pressing were inves... To improve the mechanical properties of WC-Al2O3 composites, the effects of trace amount of CeO2 additives on the microstructure and mechanical properties of the WC-Al2O3 composites prepared by hot pressing were investigated. The results revealed that the WC-Al2O3 composites doped with 0.1% CeOz possessed refined microstructure and enhanced mechanical properties compared with that of the undoped WC-Al2O3composites. Trace CeO2 suppressed the decarburization of WC, promoted the microstructural refinement, and improved the interface coherence of the WC matrix and Al2O3. When 0.1% CeO2 was added to the WC-Al2O3 composites, the effect of CeO2 resulted in the achievement of a relative density of 98.82% with an excellent Vickers hardness of 16.89 GPa, combining a fracture toughness of 9.85 MPa. m1/2 with an acceptable flexural strength of 1 024.05 MPa. 展开更多
关键词 ceo2 additives microstructure mechanical properties WC-Al2o3 composites
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磁性纳米CeO_2/Fe_3O_4非均相Fenton反应催化降解氧氟沙星 被引量:8
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作者 胡晓丹 周志伟 +2 位作者 张伟 张晓红 张海黔 《无机材料学报》 SCIE EI CAS CSCD 北大核心 2016年第6期613-620,共8页
为了提高Fe_3O_4的催化活性,制备了磁性CeO_2/Fe_3O_4复合纳米粒子,构成非均相Fenton反应体系,催化降解水环境中的氧氟沙星抗生素。研究了CeO_2含量、H_2O_2浓度、pH等因素对CeO_2/Fe_3O_4非均相催化活性的影响,并通过溶出铁离子测定、... 为了提高Fe_3O_4的催化活性,制备了磁性CeO_2/Fe_3O_4复合纳米粒子,构成非均相Fenton反应体系,催化降解水环境中的氧氟沙星抗生素。研究了CeO_2含量、H_2O_2浓度、pH等因素对CeO_2/Fe_3O_4非均相催化活性的影响,并通过溶出铁离子测定、动力学拟合等方式对反应机理进行探究。结果表明,CeO_2/Fe_3O_4较Fe_3O_4具有更强的催化活性,氧氟沙星的降解率随CeO_2含量、H_2O_2浓度和溶液酸度的增加而提高,当H_2O_2浓度为100 mmol/L以及pH为3时,CeO_2/Fe_3O_4(摩尔比=0.780)-H_2O_2体系催化降解氧氟沙星的效果最佳。CeO_2/Fe_3O_4体系催化降解氧氟沙星反应遵循一级反应动力学方程,反应机理主要为催化剂表面的催化反应,同时CeO_2产生氧空位的电子转移对Fe_3O_4的催化反应起到协同强化的作用。 展开更多
关键词 FE3o4 ceo2 降解 氧氟沙星
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桉树遗态Fe_2O_3-Fe_3O_4/C复合材料的制备及其对水中锑(Ⅲ)的吸附研究 被引量:6
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作者 韦文慧 朱宗强 +2 位作者 朱义年 秦辉 梁美娜 《水处理技术》 CAS CSCD 北大核心 2013年第5期69-72,共4页
以桉树为植物模板,通过氨水浸提、硝酸铁浸渍和马弗炉有氧焙烧等处理制备获取桉树遗态Fe2O3-Fe3O4/C复合材料,借助扫描电镜和X射线衍射分析仪等手段对其进行了结构和性质分析;通过吸附试验研究了初始Sb(Ⅲ)含量、pH、吸附剂投加量以及... 以桉树为植物模板,通过氨水浸提、硝酸铁浸渍和马弗炉有氧焙烧等处理制备获取桉树遗态Fe2O3-Fe3O4/C复合材料,借助扫描电镜和X射线衍射分析仪等手段对其进行了结构和性质分析;通过吸附试验研究了初始Sb(Ⅲ)含量、pH、吸附剂投加量以及吸附剂粒径对吸附效果的影响。结果表明,获取的复合材料很好地保留了桉树自身固有的植物本征结构,且Fe2O3和Fe3O4是其主要组成部分,呈现出其对水中Sb(Ⅲ)的良好吸附性能;随着Sb(Ⅲ)初始含量的增加,桉树遗态Fe2O3-Fe3O4/C复合材料对Sb(Ⅲ)的吸附量增大;温度对吸附除Sb(Ⅲ)没有明显影响;初始溶液pH为8时,Sb(Ⅲ)的去除效果最好;适宜吸附剂投加量为0.5 g/50 mL;吸附剂粒径小利于吸附率的提高,但块状材料也显示出良好的吸附性能。 展开更多
关键词 桉树遗态 Fe2o3-fe3o4 C复合材料 制备 吸附
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Si_3N_4-Fe对Al_2O_3-SiC-C质铁沟浇注料性能的影响 被引量:15
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作者 邓小玲 孙加林 +2 位作者 陈俊红 张厚兴 洪彦若 《耐火材料》 CAS 北大核心 2004年第2期82-84,共3页
利用Si3N4 的优良性质及金属塑性相Fe的作用 ,将其添加到高炉出铁沟用Al2 O3-SiC -C浇注料中 ,以改善材料的力学性能和抗氧化性能。对高温处理后试样强度、显气孔率测试以及对氧化层的SEM分析 ,结果表明 ,添加适量的Si3N4 -Fe ,材料的... 利用Si3N4 的优良性质及金属塑性相Fe的作用 ,将其添加到高炉出铁沟用Al2 O3-SiC -C浇注料中 ,以改善材料的力学性能和抗氧化性能。对高温处理后试样强度、显气孔率测试以及对氧化层的SEM分析 ,结果表明 ,添加适量的Si3N4 -Fe ,材料的显气孔率降低 ,强度提高 ,抗氧化性增强。 展开更多
关键词 Si3N4-fe AL2o3 SIC 铁沟浇注料 力学性能 抗氧化性能 显气孔率测试 氧化层
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纳米Al_2O_3-Fe_3O_4/FeS固体润滑复合层减摩润滑机理 被引量:7
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作者 胡春华 杨春燕 +3 位作者 刘庆存 孙志杰 马世宁 乔玉林 《材料热处理学报》 EI CAS CSCD 北大核心 2013年第6期130-135,共6页
采用离子氮碳共渗与离子渗硫复合处理技术在45钢表面形成FeS固体润滑复合层,然后采用真空浸渍方法将纳米Al2O3和Fe3O4颗粒置入复合层的微纳孔隙中,制备成纳米Al2O3-Fe3O4/FeS固体润滑复合层。在10~60 N的载荷下,纳米Al2O3-Fe3O4/FeS固... 采用离子氮碳共渗与离子渗硫复合处理技术在45钢表面形成FeS固体润滑复合层,然后采用真空浸渍方法将纳米Al2O3和Fe3O4颗粒置入复合层的微纳孔隙中,制备成纳米Al2O3-Fe3O4/FeS固体润滑复合层。在10~60 N的载荷下,纳米Al2O3-Fe3O4/FeS固体润滑复合层表现出优良的减摩与耐磨性能。这是因为,一方面磨损表面生成的化学反应膜,起到了固体润滑和阻碍摩擦表面间金属直接接触的作用;另一方面在摩擦过程中,纳米Al2O3-Fe3O4/FeS固体润滑复合层中的纳米Al2O3和Fe3O4颗粒起到了'微纳滚珠'作用,微观上将'滑动摩擦'部分转变为'滚动摩擦',且纳米颗粒预先置入复合膜层中,在摩擦过程中不易流失,延长了其'微纳滚珠'的作用,从而使其摩擦因数(载荷60 N时)及体积磨损量比涂抹纳米Al2O3/Fe3O4复合添加剂润滑的FeS固体润滑复合层分别降低了7.2%和50%。 展开更多
关键词 FeS固体润滑复合层 纳米Al2o3-fe3o4 化学反应膜 减摩耐磨 润滑机理
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微波催化剂MgFe_2O_4-Fe_2O_3微波催化氧化降解结晶紫废水 被引量:7
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作者 高令飞 蒋尊芳 +2 位作者 周继承 殷诚 尹静雅 《湖南大学学报(自然科学版)》 EI CAS CSCD 北大核心 2015年第12期74-79,共6页
提出一种新型的、无需添加氧化剂处理结晶紫废水的方法.通过共沉淀晶化法制备微波催化剂MgFe_2O_4-Fe_2O_3,在微波辐照下降解结晶紫废水,考察了催化剂用量、微波功率、辐照时间对结晶紫去除率的影响.结果表明:在一定条件下,去除率随着... 提出一种新型的、无需添加氧化剂处理结晶紫废水的方法.通过共沉淀晶化法制备微波催化剂MgFe_2O_4-Fe_2O_3,在微波辐照下降解结晶紫废水,考察了催化剂用量、微波功率、辐照时间对结晶紫去除率的影响.结果表明:在一定条件下,去除率随着催化剂用量的增加、微波功率的增大、微波辐照时间的延长而增加.当微波功率为800 W,辐照时间5min,催化剂用量1g/L时,处理200mg/L的结晶紫废水,去除率可达99.3%.本文还对微波催化氧化机理进行了探究,通过添加不同氧化基团清除剂的实验发现,氧化基团清除剂的添加降低了结晶紫的去除率,并提出了该反应的微观机理:微波催化剂吸收电磁波发生光电效应,产生电子和空穴对,与水等作用产生·OH,·OH再氧化降解废水中的有机物. 展开更多
关键词 微波催化 微波催化剂 MgFe2o4-fe2o3 羟基自由基(·oH) 结晶紫废水
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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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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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磁性Fe_3O_4/α-Fe_2O_3核壳材料降解水中亚甲基蓝 被引量:4
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作者 于文肖 罗鸣 +3 位作者 马争 赵恒新 刘辉 魏雨 《河南师范大学学报(自然科学版)》 CAS 北大核心 2016年第2期95-101,共7页
以Fe_3O_4为核,以α-Fe_2O_3为壳层,合成出一种核壳结构的Fe_3O_4/α-Fe_2O_3纳米复合材料.采用扫描电镜(SEM)、透射电镜(TEM)和X-射线衍射仪(XRD)等表征手段对核壳材料的形貌、组成及结构等进行了表征,并将其应用于亚甲基蓝溶液... 以Fe_3O_4为核,以α-Fe_2O_3为壳层,合成出一种核壳结构的Fe_3O_4/α-Fe_2O_3纳米复合材料.采用扫描电镜(SEM)、透射电镜(TEM)和X-射线衍射仪(XRD)等表征手段对核壳材料的形貌、组成及结构等进行了表征,并将其应用于亚甲基蓝溶液的降解.结果表明:核壳结构的Fe_3O_4/α-Fe_2O_3纳米粒子粒径约为50-80nm.当H_2O_2用量为0.23mol/L,Fe_3O_4/α-Fe_2O_3投加量为5g/L,pH值为2,亚甲基蓝溶液初始质量浓度为5.0mg/L,60min内亚甲基蓝的降解可达98.7%.Fe_3O_4/α-Fe_2O_3纳米粒子经过3次循环使用后,对亚甲基蓝仍具有较好的降解能力. 展开更多
关键词 核壳结构 Fe3o4-fe2o3 磁性 亚甲基蓝 降解
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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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α-Fe_2O_3/Fe_3O_4复合负极材料的制备与电化学性能研究 被引量:4
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作者 石磊 刘洪波 +2 位作者 何月德 洪泉 杨丽 《功能材料》 EI CAS CSCD 北大核心 2010年第1期177-180,共4页
通过固相反应法合成出α-Fe2O3/Fe3O4复合产物,利用XRD、Raman、SEM等技术和恒电流充放电方法,探讨了恒温反应时间对材料微观结构、形貌以及电化学性能的影响。研究表明,恒温反应时间对复合产物中各组分的相对含量、形貌与电化学性能影... 通过固相反应法合成出α-Fe2O3/Fe3O4复合产物,利用XRD、Raman、SEM等技术和恒电流充放电方法,探讨了恒温反应时间对材料微观结构、形貌以及电化学性能的影响。研究表明,恒温反应时间对复合产物中各组分的相对含量、形貌与电化学性能影响较大;除首次循环外,复合负极材料在随后充放电过程中库伦效率可达96%以上,循环性能与倍率性能明显优于单相α-Fe2O3负极材料与Fe3O4负极材料。 展开更多
关键词 锂离子电池 复合负极材料 α-fe2o3/Fe3o4
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