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316L Austenite Stainless Steels Strengthened by Means of Nano-scale Twins

G.Z. Liu N.R. Tao K. Lu

材料科学技术(英文)

By means of dynamic plastic deformation (DPD) followed by thermal annealing, a mixed structure of micro-sized austenite grains embedded with nano-scale twin bundles (of about 20% in volume) has been synthesized in a 316L stainless steel (SS). Such a 316L SS sample exhibits a tensile strength as high as 1001 MPa and an elongation-to-failure of about 23%. The much elevated strength originates from the presence of a considerable number of strengthening nano-twin bundles, while the ductility from the recrystallized grains. The superior strength-ductility combination achieved in the nano-twins-strengthened austenite steel demonstrates a novel approach for optimizing the mechanical properties in engineering materials.

关键词: Nano-scale twins , Strength-ductility combination , Dynamic plastic deformation (DPD) , Stainless steels

Bi3+,Eu3+,Tb3+掺杂Lu3TaO7的发光性能研究

刘文鹏 , 张庆礼 , 杨华军 , 周鹏宇 , 孙敦陆 , 高进云 , 谷长江 , 罗建乔 , 王迪 , 殷绍唐

量子电子学报 doi:10.3969/j.issn.1007-5461.2011.02.018

采用固相反应法制备了Bi3+、Eu3+、Tb3+掺杂的Lu3TaO7.测量了样品的X射线衍射谱、激发和发射光谱及荧光衰减曲线.三种离子掺杂的Lu3TaO7均呈现出强的荧光发射,其中Bi3+具有峰位在431 nm处的一强发射宽带,衰减寿命为16.8μs,Eu3+、Tb3+则表现出稀土离子的特征锐发射峰,衰减寿命分别为1.26 ms和1.20 ms.因此,它们均是具有潜在应用前景的重闪烁体材料.

关键词: 材料 , 闪烁体 , Lu3TaO7 , 发光

Z型复合催化剂g-C3N4/Vo-ZnO光催化活性的研究

刘亚男 , 王瑞霞 , 杨正坤 , 杜虹 , 姜一帆 , 申丛丛 , 梁况 , 徐安武

催化学报 doi:10.1016/S1872-2067(15)60985-8

随着科学技术的不断进步和经济的快速发展,人类对自然资源的需求量越来越大,在开发利用自然资源的同时,大量的有机污染物也随之进入自然环境.这些物质不仅污染环境、破坏生态,更对人类的生活和健康带来了巨大的威胁.研究证实,半导体光催化剂在光照条件下可以破坏有机污染物的分子结构,最终将其氧化降解成CO2、H2O或其它不会对环境产生二次污染的小分子,从而净化水质.近年来,有关光催化降解有机污染物的报道日益增多. ZnO作为一种广泛研究的光催化降解材料,因其无毒、低成本和高效等特点而具有一定的应用前景.但是ZnO较大的禁带宽度(3.24 eV)导致其只能吸收紫外光部分,而对可见光的吸收效率很小,极大地制约了其实际应用.除此之外, ZnO受光激发产生的电子-空穴分离效率较低、光催化过程中的光腐蚀严重也是制约其实际应用的重要因素.为了提高ZnO的光催化活性和稳定性,本文合成了用g-C3N4修饰的氧空位型ZnO(g-C3N4/Vo-ZnO)复合催化剂,在有效调控ZnO半导体能带结构的同时,通过负载一定量的g-C3N4以降低光生电子-空穴对的复合速率和反应过程中ZnO的光腐蚀,增强催化剂的光催化活性和稳定性.本文首先合成前驱体Zn(OH)F,然后焙烧三聚氰胺和Zn(OH)F的混合物得到g-C3N4/Vo-ZnO复合催化剂,并采用电子顺磁共振波谱(EPR)、紫外-可见光谱(UV-vis)、高分辨透射电镜(HRTEM)和傅里叶变换红外光谱(FT-IR)等表征了它们的结构及其性质. EPR结果表明,ZnO焙烧后具有一定浓度的氧空位,导致其禁带宽度由3.24 eV降至3.09 eV,因而提高了ZnO对可见光的吸收效率. UV-vis结果显示, Vo-ZnO复合g-C3N4后对可见光的吸收显著增强. HRTEM和FT-IR结果均表明, g-C3N4纳米片和Vo-ZnO颗粒之间通过共价键形成了强耦合,这对g-C3N4/Vo-ZnO复合催化剂中光生载流子的传送和光生电子-空穴对的有效分离起到重要作用.可见光催化降解甲基橙(MO)和腐殖酸(HA)的实验进一步证明, g-C3N4/Vo-ZnO复合材料具有较好的光催化活性,优于单一的g-C3N4或Vo-ZnO材料.同时还发现, g-C3N4的负载量对光催化活性有显著影响,当氮化碳的负载量为1 wt%时,所制材料具有最高的光催化活性:可见光照射60 min后,MO降解率可达到93%, HA降解率为80%.复合材料光催化活性的增强一方面是因为氧空位的形成减小了ZnO的禁带宽度,使得ZnO对可见光的吸收能力大大增强;另一方面, g-C3N4和Vo-ZnO的能带符合了Z型催化机理所需的有效能带匹配,使得光生电子-空穴对得到了有效的分离,从而提高了光催化活性.降解MO的循环实验表明, g-C3N4/Vo-ZnO催化剂具有很好的稳定性且不容易发生光腐蚀.与此同时,我们对比了用不同方法制备的g-C3N4/ZnO材料的催化性能.结果显示,本文制备的g-C3N4/Vo-ZnO复合材料具有更好的降解效率.总体而言,对于降解有机污染物, g-C3N4/Vo-ZnO可能是一个更为有效可行的催化体系.此外,本文也为设计与制备其他新型光催化剂提供了一条新的思路.

关键词: 氧空位氧化锌 , 石墨化氮化碳 , 复合光催化剂 , 光降解 , Z

Phase segregation and its effect on the adhesion of Cr-Al-N coatings on K38G alloy prepared by magnetron sputtering method

Surface & Coatings Technology

Cr1-xAlxN (0K38G alloy. The composition and microstructure of the coatings were investigated. Phase segregation of cubic AIN was considered in Cr0.65Al0.35N using X-ray diffraction analyses. This segregation of cubic AIN from CrAIN matrix might be induced by the high micro-stress. The critical failure load determined by scratch tests of the coating with c-AIN segregation was highest among all the coatings studied in the present work, which indicated that the coating has the best adhesion. (C) 2007 Elsevier B.V. All rights reserved.

关键词: Cr(1-x)Al(x)n coatings;cubic AlN segregation;residual stress;scratch;test;cathodic arc evaporation;aluminum nitride;hard coatings;high-pressure;thin-films;cubic-aln;mechanical-properties;transition;superlattices;stress

Oxidation resistance of a Cr0.50Al0.50N coating prepared by magnetron sputtering on alloy K38G

Oxidation of Metals

A Cr0.50Al0.50N coating has been prepared by a reactive-magnetron-sputtering method on alloy K38G. The coating possesses mainly the B1 type with a small amount of B4-type crystal structure phase. Isothermal oxidation tests were performed at 900-1,100 degrees C for 20 h by thermogravimetric analysis (TGA) in air. The results reveal that the coated samples have much lower mass gain than that of the bare alloy. The parabolic rate constants of the coated samples decrease by 2 orders of magnitude compared with the bare alloy at 1,000 and 1,100 degrees C. During the oxidation of the coated samples below 1,000 degrees C, the main oxide is Cr2O3, but above 1,000 degrees C, the scale changes to alpha-Al2O3. The observed oxidation behaviors demonstrate that the Cr0.50Al0.50N coating can provide good protection against corrosion over a wide temperature range.

关键词: Cr0.50Al0.50N coating;magnetron sputtering;isothermal oxidation;oxidation mechanism;thermal barrier coatings;cyclic oxidation;high-temperature;bond-coat;microstructural development;isothermal oxidation;diffusion coatings;nitride coatings;hard coatings;behavior

利用Ni(OH)x助催化剂修饰提高g-C3N4纳米片/WO3纳米棒Z型纳米体系的可见光产氢活性的研究

何科林 , 谢君 , 罗杏宜 , 温九青 , 马松 , 李鑫 , 方岳平 , 张向超

催化学报 doi:10.1016/S1872-2067(17)62759-1

光催化技术是目前解决能源和环境问题最具前景的手段之一,因此寻找高效光催化剂已成为光催化技术的研究热点.而在众多半导体催化剂中,廉价、环保且性能稳定的g-C3N4光催化剂在太阳光开发利用方面尤其引人关注.然而,由于g-C3N4的比表面小,活性位点少,以及光生电子/空穴对易复合等不足,严重导致其较低的光催化量子效率.因此,构造Z型体系和负载助催化剂等策略被广泛应用于提高g-C3N4光催化效率.在过去几年中,TiO2,Bi2WO6,WO3,Bi2MoO6,Ag3PO4和ZnO已经被成功证实可以与g-C3N4耦合而构造Z型光催化剂体系.其中,WO3/g-C3N4光催化剂体系,具有可见光活性的WO3导带中的光生电子和g-C3N4价带中的光生空穴容易实现Z型复合,从而保留了WO3的强氧化能力和g-C3N4的高还原能力,最终大幅度提高了整个体系的光催化活性.在g-C3N4的各种产氢助催化剂中,由于常用的Pt,Ag和Au等贵金属的高成本和低储量等问题严重限制了它们的实际应用,所以近年来各种非贵金属助催化剂(包括纳米碳,Ni,NiS,Ni(OH)2,WS2和MoS2等)得到了广泛的关注.我们采取廉价且丰富的Ni(OH)x助催化剂修饰g-C3N4/WO3耦合形成的Z型体系,开发出廉价高效的WO3/g-C3N4/Ni(OH)x三元产氢光催化体系.在该三元体系中,Ni(OH)x和WO3分别用于促进g-C3N4导带上光生电子和价带的光生空穴的分离及利用,从而使得高能的g-C3N4的光生电子在Ni(OH)x富集并应用于光催化产氢,而高能的WO3的光生空穴被应用于氧化牺牲剂三乙醇胺,最终实现了整个体系的高效光催化产氢活性及稳定性.我们通过直接焙烧钨酸铵和硫脲制备出WO3纳米棒/g-C3N4,并采用原位光沉积方法将Ni(OH)x纳米颗粒负载到WO3/g-C3N4上.随后,我们采取X射线衍射(XRD)、高分辨透射电子显微镜(HRTEM)、X射线光电子能谱分析(XPS)和比表面和孔径分布等表征手段来研究光催化剂的结构与形貌;采取紫外-可见漫反射表征方法来研究其光学性能;采取荧光光谱,阻抗和瞬态光电流曲线等表征手段来测试光催化剂的电荷分离性能;采取极化曲线和电子自旋共振谱等表征手段来证明光催化机理;采取光催化分解水产氢的性能测试来研究光催化剂的光催化活性与稳定性.XRD,HRTEM和XPS表征结果,表明WO3为有缺陷的正交晶系的晶体,直径为20–40纳米棒且均匀嵌入在g-C3N4纳米片上;Ni(OH)x为Ni(OH)2与Ni的混合物,其Ni(OH)2与Ni的摩尔比为97.4 : 2.6,Ni(OH)x粒径为20–50 nm且均匀分散在g-C3N4纳米片上,WO3/g-C3N4/Ni(OH)x催化剂界面之间结合牢固,其中WO3和Ni(OH)x均匀分布在g-C3N4上.紫外-可见漫反射表征结果表明,随着缺陷WO3的负载量增加,复合体系的吸收边与g-C3N4相比产生明显的红移,而加入Ni(OH)x助催化剂使得催化剂体系的颜色由黄变黑,明显地增加了可见光的吸收.荧光光谱,阻抗和瞬态光电流曲线结果表明,WO3和Ni(OH)x的加入能有效地促进光生电子/空穴的分离.极化曲线结果表明,掺入WO3和Ni(OH)x能降低g-C3N4的析氢过电位,从而提高光催化剂表面的产氢动力学.?O2?和?OH 电子自旋共振谱表明成功形成了WO3/g-C3N4 耦合Z 型体系.光催化分解水产氢的性能测试表明,20%WO3/g-C3N4/4.8%Ni(OH)x产氢效率最高(576 μmol/(g?h)),分别是g-C3N4/4.8%Ni(OH)x,20%WO3/g-C3N4和纯g-C3N4的5.7,10.8和230倍.上述结果充分证明,Ni(OH)x助催化剂修饰和g-C3N4/WO3 Z型异质结产生了极好的协同效应,最终实现了三元体系的极高的光催化产氢活性.

关键词: 光催化产氢 , 稳定的Ni(OH)x催化剂 , g-C3N4 , Z型体系 , 异质结

ROOM-TEMPERATURE MAGNETIC-ANISOTROPY OF RARE-EARTH TRANSITION-METAL INTERMETALLICS R2FE14C (R = LU, GD, ND) AND R2FE14B (R = GD, ND)

Solid State Communications

Magnetic anisotropy fields at room temperature of ternary tetragonal compounds of R2Fe14C(R = Lu, Gd, Nd) and R2Fe14B(R = Gd, Nd) were determined by Singular-Point-Detection (SPD) technique. The magnetocrystalline anisotropies of the carbides were found to be larger than those of their corresponding borides, indicating that the outstanding permanent-magnetic properties may be obtained in the R2Fe14C-based alloys.

关键词:

TEMPERATURE-DEPENDENCE OF THE MAGNETIC-PROPERTIES OF THE RARE-EARTH TRANSITION-METAL INTERMETALLIC LU2FE14C

Journal of Magnetism and Magnetic Materials

Magnetization curves of the ternary tetragonal compound Lu2Fe14C were measured in an extracting-sample magnetometer in the temperature range from 1.5 to 300 K. The temperature dependence of the magnetic properties of Lu2Fe14C is discussed.

关键词: anisotropy

新型超硬材料z-BC2N的弹性、硬度与热导率研究

王军朋 , 李凤 , 敖靖 , 焦丽娜 , 李春梅 , 陈志谦

无机材料学报 doi:10.15541/jim20140463

采用第一性原理计算研究了超硬材料z-BC2N的弹性各向异性性质、应力-应变关系、硬度及最小热导率性质.计算得到的晶体力学行为判据 B/G 为 0.87, 泊松比为 0.084, 普适弹性各向异性指数为 0.09992.[100]晶向上最大拉伸强度达到180 GPa,(100)[010]应变方向上最大剪切强度达到160 GPa,维氏硬度值为77.07 GPa.基于Cahill模型得到的最小热导率为6.811 W/(m·K).结果表明: z-BC2N是脆性材料且力学稳定性良好,有非常高的拉伸强度、剪切强度, 体弹模量为各向同性, 杨氏模量各向异性程度不大.z-BC2N 的最小热导率低于金刚石的最小热导率.

关键词: 超硬材料 , 弹性性质 , 各向异性 , 热导率

Fabrication of Porous Si3N4-Lu2Si2O7 Composite Ceramics

Pengfei Zhang Litong Zhang Xiaowei Yin

材料科学技术(英文)

To improve the corrosion resistance of porous Si3N4 used in the high temperature environments, which contain water vapor and volatile species, porous Si3N4-Lu2Si2O7 composite ceramics were fabricated by a process of oxidation bonding and pressureless sintering in flowing N2 atmosphere at the temperatures lower than 1550°C. The pores in ceramics were formed by removing the pore-forming agent (phenolic resin). SiO2 derived by the oxidation of Si3N4 at 1250°C in air reacted with Lu2O3 at various sintering temperatures, leading to the formation of Lu2Si2O7 with excellent oxidation and corrosion resistance. The phase composition, microstructure, and mechanical properties of the porous ceramics depended on the sintering temperatures. Si3N4-Lu2Si2O7 composite ceramics with the porosity of 52% and the pore size of 0.2μm were obtained by oxidation bonding at 1250°C for 1 h and pressureless sintering at 1550°C for 2 h using 4 wt pct Lu2O3 additive.

关键词: Porous ceramics , 氮化硅 , 焦硅酸镥 , 无压烧结

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