J. Feng
,
W.D. Huang
,
X. Lin
,
T. Li
,
Y.F. Xue and Y.H. Zhou(State Key Lab. of Solidilication Processing
,
Northwestern Polytechnical University
,
Xi'an 710072
,
China)
金属学报(英文版)
In order to investigate the response of cellular spacing to the variation of growth velocity under near-rapid directional solidification condition, Al-0.53wt%Zn alloy is directionally solidified with Bridgman apparatus. The results show that at the given temperature gradient the obtained microstrvctures are all cells and there exists a wide distribution range of cellular spacing. The maximum, λmax, minimum, λmin, and average cellular spacing, λ, as functions of growth rate, V, can be given by λmax=948.51V-0.4961, λmin= 661.16V-0.5015 and λ=412.41V-0.5049, respectively. The experimental results are compared with that predicted by KGT model, and a good agreement is found. Moreover,it is found that the average cellular spacing is also remarkably history-dependent.
关键词:
Al-Zn alloy
,
null
,
null
,
null
杨梅
,
刘其鹏
,
李东风
,
尤洪鹏
,
洪广言
中国稀土学报
以Y2O3,Yb2O3,Er2O3,NH4F等试剂为原料,采用水热法在180 ℃下保温10 h获得了NH4Y1.56Yb0.4Er0.04F7球形纳米粒子. 所获得的纳米粒子在氮气保护下400 ℃灼烧2 h,制备出Y0.78Yb0.2Er0.02F3纳米粒子. 利用Scherrer公式计算出NH4Y2F7:Yb3+,Er3+和YF3:Yb3+,Er3+的粒径分别为65.8和68.3 nm. TEM照片展示粒子近球形,其大小与Scherrer公式计算结果一致. TEM还揭示每个粒子上面应带有许多小孔. 氮气吸附脱附实验进一步证实了粒子上存在小孔. 在980 nm的红外激光激发下,NH4Y1.56Yb0.4Er0.04F7不发光,而Y0.78Yb0.2Er0.02F3发出明亮的绿光,表明所获得的Y0.78Yb0.2Er0.02F3具有强的上转换发光.
关键词:
NH4Y1.56Yb0.4Er0.04F7
,
Y0.78Yb0.2Er0.02F3
,
纳米粒子
,
水热法
,
上转换发光
,
稀土
Transactions of Nonferrous Metals Society of China
The microstructure evolution of an extruded Mg-8.57Gd-3.72Y-0.54Zr (mass fraction, %, GW94) alloy during reheating into the semisolid state was investigated using optical microscopy (OM), scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDX). Typical semisolid microstructure with globular solid particles distributed in the liquid matrix is obtained over 600 C. The solid content of (Gd+Y) in the primary alpha-Mg particles decreases with increasing the semisolid temperature. With the prolongation of isothermal holding time, the liquid fraction does not change significantly, while the grains grow up and spheroidize. Three methods used to determine the liquid fraction as a function of temperature, namely quantitative metallography on quenched microstructures, cooling curve thermal analysis, and thermodynamic calculations were further compared.
关键词:
semisolid;Mg-Gd-Y alloy;partial remelting;microstructural evolution;magnesium alloy;fraction;system
Yan NIU
,
Weitao WU and Chaoliu ZENG (State Key Lab. for Corrosion and Protection
,
Institute of Corrosion and Protection of Metals
,
Chinese Academy of Sciences
,
Shenyang 110015
,
China)F. Gesmundo and F. Viani (Instituto di Chimica
,
Facolta di Ingegneria
,
Un
材料科学技术（英文）
The corrosion of an Fe-based alloy containing 15 wt pct Y in H2-H2S mixtures under 10-3 Pa S2 was studied at 600~800℃ in an attempt to find materials with improved sulphidation resistance with respect to pure Fe. The presence of Y has been shown to be beneflcial, but not sufficient to the level expected. In fact, the alloy is able to form at all tested temperatures an external FeS layer, beneath which a zone containing a mixture of the two sulphides is also present. Thus,Fe can still diffuse through this region to form the outer FeS layer with non-negligible rate. The corrosion rate of Fe is considerably reduced by the Y addition. but the alloy corrodes still much more rapidly than Y. The sulphidation kinetics is generally rather irregular for both the pure metals, while the corrosion rate of the alloy decreases with time and tends to become parabolic after an initial period of 12~17 h. The sulphidation behaviour of the alloys is discussed by taking into account the presence of an intermetallic compound Fe17Y2 and the limited solubility of Y in Fe
关键词:
材料科学技术（英文）
The corrosion of an Fe-based alloy containing 15 wt pet Y in H-2-H2S mixtures under 10(-3) Pa S-2 was studied at 600 similar to 800 degrees C in an attempt to find materials with improved sulphidation resistance with respect to pure Fe. The presence of Y has been shown to be beneficial, but not sufficient to the level expected. In fact, the alloy is able to form at all tested temperatures an external FeS layer, beneath which a zone containing a mixture of the two sulphides is also present. Thus, Fe can still diffuse through this region to form the outer FeS layer with non-negligible rate. The corrosion rate of Fe is considerably reduced by the Y addition, but the alloy corrodes still much more rapidly than Y. The sulphidation kinetics is generally rather irregular for both the pure metals, while the corrosion rate of the alloy decreases with time and tends to become parabolic after an initial period of 12 similar to 17 h. The sulphidation behaviour of the alloys is discussed by taking into account the presence of an intermetallic compound Fe17Y2 and the limited solubility of Y in Fe.
关键词:
high-temperature sulfidation;most-reactive component;ni-nb alloys;h2-h2s mixtures;behavior;600-degrees-c-800-degrees-c;oxidation
NIU Yan
,
F.GESMUNDO
,
WU Weitao
,
ZENG Chaoliu
,
F.VIANI
,
(State Key Laboratory for Corrosion and Protection
,
Institute of Corrosion and Protection of Metals
,
Chinese Academy of Sciences
,
Shenyang.110015
,
China)(Istituto di Chimica
,
Facolta'di Ingegneria
,
Universita'di Genova
,
Fiera del Mare
,
Pad.D
,
16129 Genova
,
Italy)Manuscript received 3 July 1995
金属学报(英文版)
The corrosion properties of a Co-15wt% Y alloy were studied in H_2-H_2S mixtures under a sulfur pressure of 10-3 Pa at 600-800℃ and of 10-2 Pa at 800℃ to examine the effect of Y on the resistance of pure cobalt to sulfur attack at high temperatures.The alloy is nearly single-phase.containing mostly the intermetallic compound Co17Y2 plus a little amount of the solid solution of Y in cobalt.At 600-700℃ and at 800℃ under 10-2 Pa of S2 the alloy forms multi-layered scales consisting of an outer region of pure cobalt sulfide,an intermediate region of a mixture of the sulfides of the two metals and finally an innermost layer of a mixture of yttrium sulfide with metal cobalt.At 800℃ under 10-3Pa of S2,below the dissociation pressure of cobalt sulfide, the alloy forms only a single layer composed of a mixture of metallic cobalt with yttrium sulfide.Pure Y produces only the oxysulfide Y2O2S, as a result of the good stability of this compound and of the presence of some impurities in the gas mixtures used The corrosion kinetics is generally rather complex and irregular except al 800℃under 10-3 Pa of S2.The addition of yttrium always reduces the sulfidation rate of cobalt, even though the formation of a continuous protective external layer of yttrium sulfide is never achieved.The internal sulfidation of Y in Co-15% Y is not associated with a depletion of Y in the alloy.This kind of diffusionless internal attack is typical of alloys with a very small solubility of the most reactive component Y in the base metal A.which restricts severely the Y flux from the alloy towards the alloy-scale interface.
关键词:
:cobalt-yttrium alloy
,
null
,
null
王逸群
,
宋鹏
,
季强
,
廖红星
,
陆建生
材料工程
doi:10.11868/j.issn.1001-4381.2015.000379
分别利用真空等离子沉积和超音速火焰喷涂技术制备含有Y和含Y氧化物的NiCoCrAl涂层,用差热分析和光学及电子显微镜研究两种涂层在Ar-16.7%O2,Ar-3.3%H2O和Ar-0.2%H2-0.9%H2O气氛中1100℃时的氧化动力学和断面微观结构,通过第一性原理计算对比在不同气氛中含Y氧化物对涂层氧化的影响机理.结果表明:对于NiCoCrAl+Y涂层,Y倾向于向界面扩散并在界面富集导致Al2O3膜生成更多有利于内氧化的孔洞,水蒸气更会对内氧化产生促进作用.而对于NiCoCrAl+Y(O)涂层,由于Y在涂层制备过程中被氧钉扎,导致NiCoCrAl+Y(O)涂层在上述气氛中生成了平直而均匀的Al2O3层,不同气氛对其氧化行为影响较小.上述研究进一步揭示NiCoCrAl涂层中活性元素Y的存在状态和氧化气氛中的水蒸气对氧化铝组织结构和生长速率有重要影响.
关键词:
含钇氧化物
,
水蒸气
,
NiCoCrAl涂层
,
热障涂层
,
内氧化
由芳田
,
黄世华
,
王大伟
,
黄艳
,
徐建华
中国稀土学报
利用水热方法合成出RbLn2F7(Ln=Gd,Y,Er,Yb和Lu),均为六方RbEr2F7型结构.掺杂Eu3+离子样品的光谱表明水热产物中氧杂质含量极低.在RbGd2F7:Eu3+(0.5mol%)的激发光谱中只观测到Gd3+离子f-f跃迁,Eu3+离子的激发跃迁很弱.激发Gd3+离子到6IJ能级后,观测到Eu3+离子的特征发射,Gd3+离子与Eu3+离子之间存在能量传递过程.Eu3+离子的5D0→7F1和5D0→7F2跃迁发射较强,表明稀土离子在六方RbLn2F7中处于非中心对称的格位.
关键词:
RbLn2F7
,
水热合成
,
真空紫外(VUV)
,
氟化物
,
能量传递
,
稀土
