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
肖瑗
,
王哲飞
,
龚志杰
,
王丽熙
,
张其土
功能材料
采用固相合成法制备了(Y0.99R0.01)2 Ti2O7(R=Pr、Tb、Ho、Er、Tm、Yb、Lu)陶瓷,研究了Pr、Tb、Ho、Er、Tm、Yb及Lu掺杂对Y2Ti2O7陶瓷物相组成、烧结性能和微波介电性能的影响.结果表明A位取代能改进其微波介电性能.烧结样品为单相的烧绿石结构,主晶相为Y2Ti2O7.当R=Er,1450℃烧结4h时,(Y0.99Er0.01)2Ti2O7陶瓷的微波介电性能最佳:εr=44.3,Q×f=12021GHz(5.371GHz),τf=+44×10-6/℃,优于Y2Ti2O7陶瓷的介电性能(εr=54,Q×f=6565 GHz,τf=-31×10-6/℃).
关键词:
无机非金属材料
,
微波介质陶瓷
,
Y2Ti2O7
,
烧绿石结构
,
掺杂
马宏
,
彭晓东
,
谢卫东
腐蚀科学与防护技术
利用对掺法熔铸镁合金AJ61+xY, 研究了合金中相的组成和分布及其在3.5%NaCl溶液中的腐蚀行为. 结果表明, 添加稀土Y使AJ61镁合金的晶粒明显细化,Mg17Al12 相的数量明显减少且由连续网状变成弥散颗粒状分布,沿晶界处生成耐蚀稀土相Al2Y、Al3Y, AJ61镁合金的耐腐蚀性得到明显改善. 耐腐蚀性顺序为:AJ61+1.5%Y>AJ61+2.0%Y>AJ61+1.0%Y>AJ61+0.5%Y.
关键词:
Mg-6Al-1Sr 镁合金
,
yttrium
,
microstructure
,
corrosion resistance
马宏
,
彭晓东
,
谢卫东
腐蚀科学与防护技术
利用对掺法熔铸镁合金AJ61++xY,研究了合金中相的组成和分布及其在3.5%NaCl溶液中的腐蚀行为.结果表明,添加稀土Y使AJ61镁合金的晶粒明显细化,Mg17Al12相的数量明显减少且由连续网状变成弥散颗粒状分布,沿晶界处生成耐蚀稀土相Al2Y、Al3Y,AJ61镁合金的耐腐蚀性得到明显改善.耐腐蚀性顺序为:AJ61+1.5%Y＞AJ61+2.0%Y＞AJ61+1.0%Y＞AJ61+0.5%Y.
关键词:
Mg-6Al-1Sr镁合金
,
钇
,
显微组织
,
耐腐蚀
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LuxY1-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LuxY1-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)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LuxY1-xAlO3 :Ce晶体的获得.
关键词:
铝酸钇镥晶体
,
perovskite
,
garnet
,
accompany
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
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
Journal of Materials Research
Based on the best bulk metallic glass (BMG) forming alloy in the Mg-Cu-Y ternary system, we introduced Ag (or Ni) to partially substitute for Cu to improve the glass-forming ability (GFA). The objective of this paper is twofold. First, we illustrate in detail a recently developed search strategy, which was proposed but only briefly outlined in our previous publication [H. Ma, L.L. Shi, J. Xu, Y. Li, and E. Ma: Discovering inch-diameter metallic glasses in three-dimensional composition space. Appl. Phys. Lett. 87, 181915 (2005)]. The protocol to navigate in three-dimensional composition space to land large BMGs is spelled out step-by-step using the pseudo-ternary Mg-(Cu,Ag)-Y as the model system. Second, our ability to locate the best BMG former in the composition tetrahedron allows us to systematically examine, and conclude on, the effects of a given alloying element. The large improvement in glass-forming ability in the Mg-(Cu,Ag)-Y system relative to the based ternary will be contrasted with the reduced glass-forming ability in the Mg-(Cu,Ni)-Y pseudo ternary system. It is demonstrated that the improvement of glass-forming ability requires judicious choice of substitutional alloying elements and concentrations, rather than simple additions of multiple elements assuming the "confusion principle."
关键词:
bulk metallic-glass;shaped copper mold;amorphous-alloys;thermal-stability;ternary-system;casting method;p system;diameter;zr;mm
Applied Physics Letters
The structure, Curie temperature, and magnetostriction of R(1-x)Pr(x)Fe(1.85) and R(0.7)Pr(0.3)Fe(y) (R = Dy0.7Tb0.3, x less than or equal to 0.5, 1.55 less than or equal to y less than or equal to 1.85) alloys were investigated. The matrix of R(1-x)Pr(x)Fe(1.85) alloys is the MgCu2-type cubic (Dy,Tb,Pr) Fe-2 and the second phase was found to be (Dy,Tb,Pr) Fe-3 when x less than or equal to 0.3. When x>0.4, (Dy,Tb,Pr) Fe-3 is the main phase with the PuNi3-type structure and (Dy,Tb,Pr) Fe-2 becomes the minority phase. In the range of 0.32- and PuNi3-type structures coexist. The R(0.7)Pr(0.3)Fe(y) alloys contain a small amount of (Dy,To,Pr) Fe-3 phase when y>1.55, which increased with increasing y. When y = 1.55, the alloy is essentially single phase with the MgCu2-type cubic structure. The lattice parameter of (Dy,Tb,Pr) Fe-2 compound for R(1-x)Pr(x)Fe(1.85) alloys increases slowly with increasing x when x less than or equal to 0.3, and sharply increases when x>0.3. The Curie temperature of the alloys decreases steadily with increasing Pr content. The magnetostrictions of R(1-x)Pr(x)Fe(1.85) and R(0.7)Pr(0.3)Fe(y) alloys decrease with increasing Pr content and Fe content, respectively. The largest magnetostriction at room temperature was found in the alloy R(0.7)Pr(0.3)Fe(1.55) (1480 x 10(-6) at H = 796 kA/m). (C) 1996 American Institute of Physics.
关键词:
