材料期刊网

THE STUDY ON SYNTHESIS OF ULTRAFINE_α Al_2O_3 BYLOW TEMPERATURE COMBUSTION PROCESS

Z.Q. Wang1 , 2) , T.C. Ma2) , G.W. Liu2) , Y.J. Cai2) and B.L. Lu1) 1) College of Chemical Engineering , Dalian University of Technology , Dalian 116012 , China , 2) Department of Material Science and Engineering , Dalian Institute of LightIndustry , Dalian 116034 , China

金属学报(英文版)

Based on thelow temperaturecombustion synthesisof α Al2 O3 from aluminum nitrate,the effectsofthe additives on the formation and particle properties of α Al2 O3 werestudied by XRDand SEM,theinitialstudy on the manometer α Al2 O3 synthesisby LCSwas done, α Al2 O3 withtheparticlesize50 ～80 NM wasgot under properconditions.

关键词: low temperature combustion synthesis , null , null , null

L1(2)- and L1(0)-like cation-ordered structures in ZrO2-Y2O3 ceramics

Journal of Materials Research

Y0.25Zr0.75O2-x and Y0.5Zr0.5O2-y phases, with L1(2-) and L1(0-) like cation-ordered structures, respectively, have been found in ZrO2-Y2O3 ceramics in both the sintered and annealed states. High-resolution electron microscopy, energy-dispersive x-ray spectroscopy and computer simulation have been used to reveal the presence of the phases. The formation of Y0.25Zr0.75O2-x, and Y0.5Zr0.5O2-y phases was initiated during the sintering procedure and developed with the increase in annealing temperature and time. Segregation of yttrium, which was prevalent in different regions even within one grain, induced the formation of Y0.25Zr0.75O2-x and Y0.5Zr0.5O2-y phases.

关键词: yttria-stabilized zirconia;percent y2o3 alloy;x-ray-diffraction;solid-solutions;electron-diffraction;neutron-diffraction;modulated;structure;diffuse-scattering;average structure;tetragonal phase

Lu_xY_1-xAl ₃:Ce晶体中伴生(Lu,Y₃ Al₅O₁₂:Ce相成因研究

丁栋舟 , 陆晟 , 潘尚可 , 张卫东 , 王广东 , 任国浩

无机材料学报 doi:10.3724/SP.J.1077.2008.00434

采用提拉法制备了Lu_xY_1-xAlO₃:Ce晶体样品, 通过XRD物相分析和成分分析, 并结合Lu₂O ₃-Al₂O₃二元体系相图以及Lu_xY_1-x AlO₃:Ce结构稳定性方面的分析与讨论, 结果表明: 随着熔体中Lu元素含量的增加, 熔体分层加剧, 析晶Lu_xY_1-xAlO₃:Ce相的熔体组成区间将向富Lu一侧偏移, 这使得晶体上部易伴生(Lu,Y)₃Al₅O₁₂:Ce相; 而随着Lu元素含量的提高, Lu_xY_1-xAlO₃:Ce晶体的热稳定性降低, 氧空位的存在则使晶体的热稳定性进一步降低, 在接种过程中籽晶表面易发生相分解反应生成(Lu,Y)₃ Al₅O₁₂:Ce和(Lu,Y) ₄ Al₂O₉:Ce, 籽晶表面相分解产物(Lu,Y)₃Al₅O₁₂:Ce提供了诱导析晶(Lu,Y)₃Al₅O₁₂ :Ce相所需的晶核, 这使得晶体的外
表面处易伴生(Lu,Y)₃Al₅O₁₂:Ce相. 调整配料组成使 n(Lu,Y)₂O₃ ): n (Al₂O₃)=1.17～1.00, 加大熔体内部和固液界面处的温度梯度以改善熔体对流、抑制熔体分层以及籽晶表面处的相分解等有助于高Lu元素含量Lu_xY_1-xAlO₃ :Ce晶体的获得.

关键词: 铝酸钇镥晶体 , perovskite , garnet , accompany

LuxY1-xAlO3:Ce晶体中伴生(Lu,Y)3Al5O12:Ce相成因研究

丁栋舟 , 陆晟 , 潘尚可 , 张卫东 , 王广东 , 任国浩

无机材料学报 doi:10.3321/j.issn:1000-324X.2008.03.004

采用提拉法制备了LuxY1-xAlOa:Ce晶体样品,通过XRD物相分析和成分分析,并结合Lu2O3-Al2O3二元体系相图以及LuxY1-xAlO3:Ce 结构稳定性方面的分析与讨论,结果表明:随着熔体中Lu元素含量的增加,熔体分层加剧,析晶LuxY1-xAlO3:Ce相的熔体组成区间将向富Lu一侧偏移,这使得晶体上部易伴生(Lu,Y)3Al5O12:Ce相;而随着Lu元素含量的提高, LuxY1-xAlO3:Ce晶体的热稳定性降低,氧空位的存在则使晶体的热稳定性进一步降低,在接种过程中籽晶表面易发生相分解反应生成(Lu,Y)3Al5O12:Ce和(Lu,Y)4Al2O9:Ce,籽晶表面相分解产物(Lu,Y)3Al5O12:Ce提供了诱导析晶(Lu,Y)3Al5O12:Ce相所需的晶核,这使得晶体的外表面处易伴生(Lu,Y)3Al5O12:Ce相.调整配料组成使n((Lu,Y)2O3):n(A12O3)=1.17～100,加大熔体内部和固液界面处的温度梯度以改善熔体对流、抑制熔体分层以及籽晶表面处的相分解等有助于高Lu元素含量LuxY1-xAlO3:Ce晶体的获得.

关键词: 铝酸钇镥晶体 , 钙钛矿 , 石榴石 , 伴生

First-principle study of electronic properties of Ti3Si1-xAlxC2 solid solutions

Journal of Physics and Chemistry of Solids

The layered ternary ceramics Ti3SiC2 and Ti3AlC2 are isostructural and can form Ti3Si1-xAlxC2 solid solutions combining the advanced properties of both compounds [H.B. Zhang, Y.C. Zhou, Y.W. Bao, M.S. Li, Improving the oxidation resistance of Ti3SiC2 by forming a Ti3Si0.90Al0.1C2 solid solution, Acta Mater. 52 (2004) 3631-3637; E.D. Wu, J.Y. Wang, H.B. Zhang, Y.C. Zhou, K. Sun, Y.J. Xue, Neutron diffraction studies of Ti3Si0.9Al0.1C2 compound, Mater. Lett. 59 (2005) 2715-2719; J.Y. Wang, Y.C. Zhou, First-principles study of equilibrium properties and electronic structure of Ti3Si0.75Al0.25C2 solid solution, J. Phys.: Condens. Matter 15 (2003) 5959-5968; Y.C. Zhou, J.X. Chen, J.Y. Wang, Strengthening of Ti3AlC2 by incorporation of Si to form Ti3Al1-xSixC2 solid solutions, Acta. Mater. 54 (2006) 1317-1322]. In the present work, the solid solutions of Ti3Si1-xAlxC2 (x = 0, 0.25, 0.33, 0.5, 0.67, 0.75, 1) are investigated by first-principle calculations based on pseudo-potential plan-wave method within the density functional theory framework. The results show that as Al content increases in the solid solution, all the bonds have weakened to certain extents, which lead to an unstable structure both energetically and geometrically. The calculated results are compared and discussed with the reported data for the Ti3Si1-xAlxC2 solid solutions. (c) 2007 Elsevier Ltd. All rights reserved.

关键词: ceramics;ab initio calculations;electronic structure;electrical;conductivity;oxidation behavior;mechanical-properties;ti3sic2;temperature;ti3alc2;air;si

Tunable magnetocaloric effect around hydrogen liquefaction temperature in Tb(1-x)Y(x)CoC(2) compounds

Physica B-Condensed Matter

The magnetic properties and magnetocaloric effect of Tb(1-x)Y(x)CoC(2) (x = 0, 0.1, 0.2, 0.3, 0.4) compounds have been investigated systematically. All the compounds undergo second-order transitions from paramagnetic to ferromagnetic states without thermal and magnetic hysteresis. With increasing Y content from 0 to 0.4, the Curie temperatures decrease nearly linearly from 28 to 18 K. The nature of the second-order phase transitions can be confirmed by Arrott plots. For Tb(0.6)Y(0.4)CoC(2) compound, the maximum value of the magnetic entropy change -Delta S(M) at 20 K is 9.35 J kg(-1) K(-1) for an external field change of 5T (5.14 J kg(-1) K(-1) for 2T). The large reversible magnetic entropy change makes Tb(0.6)Y(04)CoC(2) compound an attractive candidate for the application at hydrogen liquefaction temperature. (C) 2010 Elsevier B.V. All rights reserved.

关键词: Curie temperature;Magnetocaloric effect;Magnetic properties;ac susceptibility

Study of properties of mixed ferro-ferrimagnetic ising compounds with (A(x)B(1-x))(y)C

Communications in Theoretical Physics

The magnetic properties of the mixed ferro-ferrimagnetic compounds with (A(x)B(1-x))(y)C-z where A(z) B-z and C are three different magnetic ions and form three different sublattices, are studied by using the standard mean-field theory. The phase diagram which is related to experimental work of molecule-based ferro-ferrimagnet ((NixMn1-xII)-Mn-II)(1.5)[Cr-III(CN)(6)].zH(2)O is obtained. The magnetization curves(z) internal energy(z) and specific heat of the same mixed (A(x)B(1-x))(y)C system are also investigated.

关键词: mixed ferro-ferrimagnet;Ising model;phase diagram;internal energy;specific heat;mean-field analysis;magnetic-properties;prussian blue;alloy

H_2气氛保护热处理1J50组织结构与性能的研究

孙建春 , 盛光敏 , 陈登明 , 周安若 , 朱光俊

功能材料

1J50软磁合金的性能主要是通过H_2热处理获得的,在1130℃和H2气氛保护下对冷轧态1J50软磁合金进行了热处理.运用MATS-2010SA软磁测试仪对处理前后1J50软磁合金的磁性能进行了检测,运用金相显微镜、XRD等手段对处理前后1J50软磁合金的组织结构进行了分析.结果表明,通过H_2热处理,1J50软磁合金的矫顽力显著降低,起始磁导率和最大磁导率提高;组织结构发生明显变化,冷轧态1J50软磁合金组织为孪晶奥氏体,平均晶粒尺寸为200μm,处理过后,晶粒显著长大,平均晶粒尺寸为100μm;由于在600℃时采取了快冷,处理后1J50软磁合金中未出现大量FeNi相和FeNi_3相.

关键词: H2热处理 , 1J50 , 组织结构 , 性能

Spin orientation and spontaneous magnetostriction of multicomponent Tb(x)Dv(1-x-y)Pr(y)(Fe0.9B0.1)(1-93) laves phases

Ieee Transactions on Magnetics

The spin orientation and spontaneous magnetostriction of multicomponent TbxDy1-x-yPry(Fe0.9B0.1)(1.93) (0.10 less than or equal to x less than or equal to 0.25, 0.30 less than or equal to y less than or equal to 0.60) Laves phases were studied by step-scanning their (440) X-ray diffraction lines. The easy magnetization direction (EMD) of the Laves phases changed from the (100) to (111) axis when x was increased from 0.10 to 0.25. With increasing y, the EMD of Tb0.15Dy0.85-yPry(Fe0.9B0.1)(1.93) and Tb0.2Dy0.8-yPry(Fe0.9B0.1)(1.93) Laves phases reoriented from the (100) to (111) axis. The magnetostriction coefficient lambda(111) of TbxDy1-x-yPry(Fe0.9B0.1)(1.93) Laves phases increased with increasing x (or y) when y (or x) was kept constant.

关键词: Laves phases;magnetostriction;spin orientation;X-ray diffraction;anisotropy compensation;alloys

1mol/L HCl中不同浓度维生素B1和B6对碳钢的缓蚀性能及机理

庞雪辉 , 张玉漩 , 厉建苗

材料保护

通过研究盐酸硫胺(维生素B1),吡哆醇(维生素B6)作为缓独剂对碳钢的缓蚀行为及其作用机制,可为新型环境友好缓蚀剂的开发和应用提供一定的理论基础.利用失重法、极化曲线法和交流阻抗法、量子化学方法研究了不同浓度维生素B1和B6在1mol/L盐酸溶液中对Q235碳钢的缓蚀性能及机理.结果表明:碳钢的腐独速率随缓性剂浓度的增大而减小,维生素B1的缓蚀效率较高,缓蚀效果较好;在298K下,缓蚀剂在碳钢表面的吸附遵循Langmuir吸附等温规律,其吸附过程包括物理吸附和化学吸附;维生素B1和B6是抑制阴极为主的混合缓蚀剂,腐蚀电流密度Jcorr随缓蚀剂浓度的增加而减小;在298K下,维生素B1和B6的交流阻抗谱为单一时间常数的容抗弧、同时电荷转移阻抗Rt随缓蚀剂浓度的增加而变大,双电层电容Cdl则相反;维生素B1比B6具有较高的最高占据轨道能量E(HOMO)和较低的最低空轨道能量E(LUMO);维生素B1比B6的缓蚀效果更好.

关键词: 缓蚀机理 , 碳钢 , 维生素B1 , 维生素B6 , 盐酸溶液