A. G. Liu
,
X.F. Wang
,
L.P. Wang
,
S. Y. Wang
,
B. Y. Tang and P.K. Chu 1) Advanced Welding Production Technology National Key Laboratory
,
HIT
,
Harbin 150001
,
China 2) Department of Physics and Material Science
,
City University of Hong Kong
,
83 Tat Chee Avenue
,
Kowloon
,
Hong Kang
,
China
金属学报(英文版)
Plasma immersion ion implantation (PIII), unrestricted by sight-light process, is considered a proper method for inner surface strengthening. Two-dimensional simulation oj inner surface PIII process of cylindrical bores were carried out in this paper using cold plasma fluid model, and influence of the bore's dimension on impact energy, retained dose and uniformity of inner surface were investigated.
关键词:
plasma immersion ion implantation
,
null
,
null
,
null
X.B. Tian
,
X.F. Wang
,
A.G. Liu
,
L.P. Wang
,
S. Y. Wang
,
B. Y. Tang and P. K. Chu 1)Advanced Welding Production & Technology National Key Laboratory
,
Harbin Institute of Technology
,
Harbin 150001
,
China 2)Department of Physics & Materials Science
,
City University of Hong Kong
,
China
金属学报(英文版)
The research on plasma immersion ion implantation has been conducted for a little over ten years. Much is needed to investigate including processing technlogy, plasma sheath dynamics, interaction of plasma and surface, etc. Of the processing methods elavated temperature technique is usually used in PIII to produce a thick modified layer by means of the thermal diffusion. Meanwhile plasma ion heating is more recently developed by Ronghua Wei et al[1]. Therefore the temeperature is a critical parameter in plasma ion processing. In this paper we present the theoretical model and analysize the effect of imlantation voltage, plasma density, ion mass,etc on the temperature rise.
关键词:
plasma immersion ion implantation
,
null
,
null
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）
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）
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
王龙妹
,
杜挺
金属学报
用直接平衡法研究了1500,1550,1600℃Ni液中Y-S平衡关系,测定了钇的脱硫常数lgK_(YS)及Y,S的一阶活度相互作用系数e_S~Y与温度的关系,并进行了有关的热力学计算。由测得的数据算出Ni液中YS的标准生成自由能△G_((Y)S),钇的标准溶解自由能△G_((Y)(l)→[Y]Ni),活度系数γ_Y~o,以及钇的克原子分数自相互作用系数∑_Y~Y和百分浓度自相互作用系数e_Y~Y与温度的关系。 对于反应[Y]_(Ni)+[S]_(Ni)=YS_(s) △G_((Y)S)=-215000+95.53T(cal/mol)脱硫常数: lgK_(YS)=-47000/T+20.86 e_S~Y=-350200/T+179 △G_((Y)(l)→[Y]Ni)=126200-79.31T(cal/mol) lgγ_(Y)=27584/T-15.151 ∑_Y~Y=-127T05/T+69.79 e_Y~Y=-364.8/T+0.2018
关键词:
LI Guodong
,
D U Ting
,
Central Iron and Steel Research Institute
,
Ministry of Metallurgical Industry
,
Beijing
,
China LI Guodong
,
Department No.16
,
Central Iron and Steel Research Institute
,
Ministry of Metallurgical Industry
,
Beijing
,
100081
,
China
金属学报(英文版)
The thermodynamic properties of Cu-Ce-S and Cu-Y-S liquid solutions were studied by the chemical equilibrium technique at 1200℃. The equilibrium constants and the standard free energies of formation of CeS and YS were determined for the reactions: CeS=[Ce]+[S] and YS = [Y]+[S] . For the solution of Ce_(1) and Y_(l) in pure Cu according to the reactions: Ce_(1)= [Ce] and Y_(1)= [Y] , the standard free energies of solutions were obtained. The first order and second order interaction coefficients between solute elements as well as the activity coefficients γ_(Ce)~0 and γ_Y~0 in liquid Cu were also determined.
关键词:
Cu-Ce-S system
,
null
,
null
王龙妹
,
杜挺
金属学报
由低温无水电解稀土夹杂物和固体电解质定氧活度测得Ni液中钇的脱硫氧常数与温度的关系:lgKr_2o_2s=-(33146)/T+3.85,(1500-1600℃)钇的硫氧化物在Ni液中的标准生成自由能与温度的关系:2[Y]+2[O]+[S]=Y_2O_2S_(s),(1500—1600℃)△G°=151640+17.61T(cal/mol)=-634460+73.69T(J/mol)由实验测得数据经热力学分析计算得到1600℃Ni液中[Y]-[S]-[O]平衡立体图及α_o-α_s平衡相图,为理论上预测夹杂物生成的先后次序及类型提供了依据.并给出了Ni液中加钇控制夹杂物形态公式,钇的加入量与氧,硫含量之间的函数关系.
关键词:
Materials Science & Engineering C-Biomimetic Materials Sensors and Systems
The bio-corrosion properties of Mg-Zn-Mn alloys with and without Y in Hank's solution at 37 degrees C were investigated by using electrochemical test and electrochemical impedance spectra (EIS). The results of open circuit potential (OCP) and polarization tests indicated that Y could reduce the cathodic current density. A passivative stage appeared in the Tafel curve of the Y containing magnesium alloy, indicating that a passivative film was formed on the surface of the Y containing magnesium alloy. EIS results showed that the Y containing alloy had higher charge transfer resistance and film resistance, but lower double layer capacity than the alloy without the Y element. The surface reaction product identification by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) showed that the surface corrosion products were hydroxide and phosphate (Mg(3)Ca(3)(PO(4))(4)) for Mg-Zn-Mn alloy and phosphate (MgNaPO(4)) for the Y containing Mg-Zn-Mn alloys. The XPS results also showed that a Y(2)O(3) protective film was formed on the surface of the Y containing magnesium alloy which contributed mainly to the low cathodic current density and the high resistance. (C) 2009 Elsevier B.V. All rights reserved.
关键词:
Magnesium alloy;Corrosion properties;Y(2)O(3);Electrochemical;impedance spectra;Biomedical materials;quasi-crystalline particles;in-vivo corrosion;magnesium alloys;mechanical-properties;microstructure;phase
