PHASE DIAGRAM OF SYSTEM NdCl_3-LiCl-KCl

The phase diagram of system NdCl_3-LiCl-KCl has been investigated by DTA.Six surfacescorresponding to the prhnary crystallization of NdCl_3,LiCl,KCl,γ-KCl·NdCl_3,β-3KCl·NdCl_3 and 2KCl·NdCl_3 respectively,eleven univariant lines related to the sec-ondary crystallization,two ternary eutectics E_1(70.5wt-% NdCl_3+8.0wt-% KCl,360℃)and E,(5.0wt-% NdCl_3+ 53.0wt-% KCl,355℃)and one ternary peritectic P(67.0wt-% NdCl_3+10.0wt-% KCl,375℃)were found.It is also chtrified that this studyon the system NdCl_3- KCl differs from previous work in the two transition temperatures:e_1(77.0 wt-% NdCl_3,484℃),e_2(40.0wt-% NdCl_3,620℃),p(70.0wt-%NdCl_3,610℃),3KCl·NdCl_3(690℃)and two reactions:α-3KGl·NdCl_3β-3KGl·NdCl_3 (355℃)β-SKGl·NdCl_3γ-3KCl·NdCl_3 (450℃)The eutectic point e_5(31.0wt-%LiCl,460C)is determined for the pseudobinary system3KCl·NdCl_3—LiCl.     

PHASE DIAGRAM OF TERNARY SYSTEM PrCl_2-CaCl_2-MgCl_2

Three surfaces corresponding to the primary crystallization of PrCl_3,CaCl_2 andMgCl_2 respectively,3 univariant curves related to the secondary crystallization and a ternaryeutectic(44.8 wt-% PrCl_3,31.8 wt-% CaCl_2,546℃)were found in systemPrCl_3-CaCl_2-MgCl_2 by means of DTA.A reaction occurs in this system:L=PrCl_3+CaCl_2+MgCl_2.     

LIQUIDUS OF TERNARY SYSTEM LaCl_3-MgCl_2-LiCl

Two surfaces correponding to LaCl_3 and α-solid solution(MgCl_2.LiCl) respectively:and one secondary crystallization curve with a minimum M at 63.8 wt-％ LaCl_3,2.0 wt-％MgCl_2,34.2 wt-％ LiCl and 492℃ were fonud by means of DTA.In combination withliquidus determination.an approach was also made to the alteration in LnCl_3-MgCl_2-LiClsvstem,where Lu denotes La.Ce.Pr or Nd.     

PHASE DIAGRAM OF PrCl_3-SrCl_2-CaCl_2 SYSTEM

Five fields corresponding to the primary crystallization of PrCl_3,Sr_3PrCl_9,α(SrCl_2,CaCl_2),α_1(CaCl_2,SrCl_2)and α_2(SrCl_2,CaCl_2)respectively,six univariant lines relatedto the secondary crystallization,one ternary eutectic(48.0 wt-％ PrCl_3,23.5 wt-％ SrCl_2;590℃)and ternary peritectic point(45.5 wt-％ PrCl_3,24.5 wt-％ SrCl_2;614℃)were determined by DTA.Attempts were also made to explore the rule governing thealteration in the phase diagram containing rare earth chloride,formation of compoundand its stability by means of polarization and counter-polarization.     

Electrochemical codeposition of typical α+β phases Mg-Li alloys from the molten LiCl-KCl-MgCl_2 system

Electrochemical codeposition of Mg-Li alloys on molybdenum electrodes was investigated in LiCl-KCl(50 wt.%:50 wt.%) melts containing different concentrations of MgCl2 at 973 K.Cyclic voltammograms show that the underpotential deposition of lithium on pre-deposited magnesium leads to the formation of liquid Mg-Li alloys.The deposition potentials of Mg(II) and Li(I) ions gradually near each other with MgCl2 concentration decreasing.Mg-Li alloys with typical α + β phases could be obtained by potentiostatic electrolysis from LiCl-KCl melts containing 5 wt.% MgCl2 at -2.25 V vs.Ag/AgCl(cathodic current density 1.70 A·cm-2) for 2.5 h.α phase, α + β phases, and β phase Mg-Li alloys with different lithium contents were obtained by potentiostatic electrolysis from LiCl-KCl melts with the different concentrations of MgCl2.The samples were characterized by X-ray diffraction and scanning electron microscopy.     

Corrosion Behavior of 304 Stainless Steel Exposed to a Simulated Salt Lake Atmosphere

The corrosion behavior of stainless steel exposed to a simulated salt lake atmosphere has been investigated by analyzing the evolution of surface morphologies and corrosion products, the initiation and development of pits, and the electrochemical characteristics. The results indicated that(Mg_6Fe_2(OH)_(16)(CO_3)(H_2O)_(4.5))_(0.25), a layered double hydroxide, has been detected for the first time in the corrosion products formed on stainless steel exposed to a simulated salt lake atmosphere. The specimens exposed to MgCl_2 deposit conditions were corroded more severely than those exposed to NaCl deposit conditions, which was attributed to the differences in the deliquescence relative humidity and efflorescence relative humidity values of MgCl_2 and NaCl. In addition, a special corrosion morphology consisting of a concentric circle of yellowish material was observed on the specimens exposed to MgCl_2 deposit conditions, which was attributed to the formation of Mg(OH)_2, inhibiting the diffusion and migration of OH~- ions to the anode region. The maximum pit depth followed a power function with respect to corrosion time. The corrosion mechanism of stainless steel exposed to a simulated salt lake atmosphere is also discussed.     

Corrosion resistance of Ni/Al2O3 coatings in NaCl solution

Abstract

This paper presents results of a research on the corrosion resistance of composite Ni/Al₂O₃ coatings electrochemically deposited from Watts baths containing different amounts (0, 20, 100 g dm^?3) of Al₂O₃ particles. Potentiodynamic tests and electrochemical impedance spectroscopy (EIS) measurements were carried out in a 3% solution of NaCl. The coatings with about 6 wt-% of corundum, deposited from a bath with 100 g dm^?3 of a powder, showed the best protective properties. The rate of corrosion of such coatings after 7 days of exposure in the NaCl solution was over two times slower than that of coatings containing 2 wt-% of Al₂O₃ and six times slower than that of a standard nickel coating. Two equivalent circuits: one consisting of two RC circuits and the other one made up of three RC circuits were used for the analysis of the impedance spectra. Regardless of the presence and amount of the Al₂O₃ particles in the nickel coating, during first day of exposure in the NaCl solution a layer of nickel oxides and hydroxides forms on the surface of the coatings increasing their corrosion resistance. In the case of coatings with 6 wt-% of Al₂O₃, the passive layer is least vulnerable to the aggressive action of Cl^? ions.     

MECHANISM OF SLOW CRACK GROWTH AND STRESS CORROSION CRACKING IN AUSTENITIC STAINLESS STEEL

通过金相跟踪观察、力学测量及断口分析,研究了奥氏体不锈钢氢致开裂和应力腐蚀的机理.结果表明,无论是不稳定型(321)还是稳定型(310)奥氏体不锈钢,电解充氢时先产生塑性变形,当它发展到临界状态时就导致氢致裂纹的形核.但在42%MgCl_2沸腾溶液中应力腐蚀时,裂纹的形核和滞后塑性变形无关.两种(321)輿氏体不锈钢应力腐蚀的门槛值K_(ISCC)远比严重充氢时氢致开裂的门槛值K_(IH)要低.两者的断口形貌也不同,应力腐蚀是解理断口,且和K_I无关.而氢致开裂断口和K_I有关,K_I高是韧窝,K_I低则获得准解理断口.实验表明,氢在奥氏体不锈钢应力腐蚀(沸腾MgCl_2介质)过程中并不起主要作用.     

Prevention of longitudinal cracks in a continuously cast slab of Fe–Cr–Ni superalloy containing Al and Ti

Abstract

The continuous casting of UNS N08811 containing Al and Ti has been established by improving the start flux. In initial trials serious longitudinal cracking appeared during the earlier stages of casting. Investigation revealed that the reaction of Al in the alloy with SiO₂ in the flux during casting, raised the Al₂O₃ content in the film after casting to 28 wt-% which is substantially higher than the 12 wt-% measured in the steady state. In the film, the major portion contained 28 wt-% Al₂O₃ and a thin layer with even lower Al₂O₃ content existed at the shell-side. The higher Al₂O₃ portion could correspond to the initial infiltration into the gap between the solidified shell and the mould. On the other hand, the layer with lower Al₂O₃ content could correspond to steady state infiltration. Initial infiltration, therefore, was estimated to be obstructed, resulting in an uneven film, because of its more viscous and glassier properties. A start flux designed with lower viscosity and higher heat generation helped to ensure even infiltration and this was shown to prevent the cracking.     

RELATIONSHIP BETWEEN REDUCIBILITY AND HIGH TEMPERATURE PROPERTIES OF TITANIA-RICH SLAGS

采用高温显微镜研究了Ti渣还原度与高温性质的关系。随着Ti渣还原度提高及FeO含量降低,其熔化性和流动性温度曲折地上升。在22.21>FeO wt-％>12.68,0FeO wt-％>5.44,0.11相似文献   

Al2O3对CaO-Al2O3-SiO2-Na2O系微晶玻璃结构与性能的影响

利用烧结法工艺制备CaO—Al2O3-SiO2-Na2O系微晶玻璃，通过DTA、XRD、IR和SEM等分析手段，系统研究Al2O3对CaO-Al2O3-SiO2-Na2O系微晶玻璃的结晶温度、晶体结构以及性能的影响。研究表明：随着Al2O3质量分数升高，初始析晶温度升高，晶体尺寸增大、析晶率升高，微晶玻璃的表观体积密度、显微硬度和抗折强度呈先增加后降低的趋势。在本实验条件下，最佳的Al2O3质量分数为11．77％。     

镁合金的活性电弧焊接

在不同的电流条件下,研究了9种常见氧化物、氟化物、氯化物活性剂在镁合金交流氩弧焊及变极性等离子焊弧中的行为.结果表明:活性剂TiO2、Cr2O3、AlF3、NiCl2、CdCl2、ZnCl2、MgCl2使镁合金交流氩弧焊焊缝熔深增加;MgF2、SiO2使镁合金交流氩弧焊焊缝熔深减小;TiO2、SiO2、Cr2O3、AlF3、NiCl2、CdCl2使镁合金变极性等离子弧焊焊缝熔深增加;MgF2、ZnCl2、MgCl2使镁合金变极性等离子弧焊焊缝熔深减小;活性剂对镁合金交流氩弧焊焊缝熔深增加的作用大于对镁合金变极性等离子弧焊的;电弧收缩是活性剂使得镁合金电弧焊焊缝熔深增加的原因之一;活性剂的加入使得焊缝的晶粒比未涂敷活性剂时粗大.     

MICROSTRUCTURE AND MAGNETIC HARDENING OF SINTERED NdFeB MAGNETS DOPPED WIHT Dy OR Dy_2O_3

The magnetic properties,microstructure and magnetic hardening of sintered(Nd_(1-x)Dy_x)_(16)Fe_(77.2)B_(6.8) and Nd_(16)Fe_(77.2)B_(6.8)+ywt-%Dy_2O_3 magnets have been stud-ied.As an addition of Dy to the magnet during smelting,Dy atoms may enter thematrix phase Nd_2Fe_(14)B,so as to enhance H_A,refine grains and improve boundary struc-ture,as well as to increase H_(ci)of the magnet.If Dy_2O_3 is added to powder materialprior to sintering,Dy atoms diffuse into the epitaxial layer of grains of matrix phasecausing enhancement of K′_1,also refinement of grains and improvement of boundarystructure.The NdFeB based permanent magnets with higher H_(ci) and greater(BH)_mmay be produced by adding about 2—3 wt-% Dy_2O_3 which make a favourable conditionfor lower cost.     

SiO2-Al2O3-CaO-Fe2O3系微晶玻璃的晶化过程

利用差热分析（ＤＴＡ）、红外吸收光谱（ＩＲ）、Ｘ射线衍射（ＸＲＤ）和扫描电镜（ＳＥＭ）等手段研究了ＳｉＯ２－Ａｌ２Ｏ３－ＣａＯ－Ｆｅ２Ｏ３系微晶玻璃晶化过程及其结晶化过程及其结晶动力学。结果表明：ＳｉＯ２－Ａｌ２Ｏ３－ＣａＯ－Ｆｅ２Ｏ３系微晶玻璃晶化过程中,初晶相是钙铁透辉石,钙铝黄长石是中间过渡相且随晶化温度的提高而消失,最终晶相只有钙铁透辉石;晶体生长指数为２．９,属三维生长。玻璃网络中主要有     

析出相对Cr-Mn-N奥氏体不锈钢应力腐蚀性能的影响

本文研究了合金碳化物M_(23)C_6和金属间化合物x相对Cr-Mn-N奥氏体不锈钢应力腐蚀性能的影响。结果指出,在4NNaCl溶液中,上述两种沉淀相对钢的自然腐蚀电位和不同电位下的断裂时间影响明显,而在45％MgCl_2溶液中,两种沉淀相的影响甚微。从断裂机制上对两种沉淀相的影响进行了讨论。     

Crystallization and properties of some CaO-Al2O3-SiO2 system glass-ceramics with Y2O3 addition

The crystallization behavior and mechanical properties of CaO-Al2O3-SiO2 （CAS） system glass-ceramics with addition of Y2O3 were investigated. The optimal sintering temperatures of all heat-treated glasses were altered and the crystallization was accelerated with Y2O3 addition, and only wollastonite as a main crystalline phase was precipitated. The volume fraction of crystalline phase and density were increased with Y2O3 addition. The results suggest that the CAS glass-ceramics would get the lowest sintering temperature and optimal microstructure with the addition of Y2O3 by 3.25 %. The bending strength has a maximum due to the oriented and interlocked wollastonite crystal, which causes crack divert or blunts to limit the further development of the flaw size and increases the surface energy of fracture.     

YNi_5 PHASE AND ITS EFFECT UPON PROPERTIES OF Ni_3Al ALLOY

An additive of Y to Ni_3Al based alloy may form a phase YNi_5 which increases in amount withthe increase of Y content.It was found that the YNi_5 phase in Ni_3Al alloy could remarkablymake its grains finer and its grain boundaries more crooked other than straight.If the Y con-tent≥0.1 wt-%,it occurs as solid solution state and is favorable to high temperaturecompressive properties and oxidation resistance of the alloy.While Y≥0.3 wt-%,the forma-tion of YNi_5 is predominant in the shape of irregular strips inside Ni_3Al grains and alongtheir grain boundaries.This seems to be quite harmful to high temperature strength,ductilityand oxidation resistance of the alloy.     

Development and tribological characterisation of nanostructured Zn-Ni and Zn-Co coatings: a comparative study

Zn-Ni and Zn-Co alloy coatings were electrodeposited on mild steel from sulphate-based baths. The morphology, microstructure, microhardness and tribological behaviours of the coatings have been studied and discussed. While the Zn-5wt-% Co layers presented a nanocrystalline simple nodular structure (45?±?5?nm), the Zn-14wt-% Ni showed a particular structure called cauliflower morphology (30?±?7?nm). The X-ray diffraction analysis showed that each of the electrodeposits was formed from zinc solid solution with a uniform zinc-cobalt intermetallic phase γ₂ (CoZn₁₃) for Zn-5wt-% Co alloy. However, a single γ-phase (intermetallic compound Ni₅Zn₂₁) was presented for the Zn-14wt-% Ni alloys. The Zn-14wt-% Ni films were found to be harder and rougher than the Zn-5wt-% Co layers. Plastic deformation and oxide layers production were the main wear mechanisms for the investigated coatings. The Zn-14wt-% Ni coatings were found to have the best wear resistance due to their microhardness and particular structure.     

冷却-加热对CaO-Al2O3-SiO2系玻璃析晶动力学的影响

以CaO-Al2O3-SiO2系玻璃为研究对象,采用Ozawa方程、Kissinger方程和JMA修正方程研究了冷却方式和加热温度对玻璃析晶动力学的影响。结果表明:化学组成相同的玻璃,冷却速度和加热温度对其析晶活化能E、Avrami指数n和析晶速率指前因子ν都有影响,但加热温度对析晶活化能E的影响更大,并在750℃出现极大值现象。通过玻璃析晶试验发现:冷却速度和加热温度对微晶玻璃主次晶相的析出没有影响,主、次晶相分别是钙长石和榍石。冷却速度和加热温度对析晶活化能E的影响主要来源于析出主、次晶相的比例不同。     

Crystallization and dielectric properties of lead-free glass-ceramic composites with Gd2O3 addition

Lead-free glass-ceramic composites in barium sodium niobate silica system with Gd2O3 addition were synthesized through melt-casting fol-lowed by controlled crystallization technique. Crystallization and dielectric properties of the Gd2O3 adding glass-ceramic composites were investigated. With the increase in the concentration of Gd2O3, the glass transition temperature and the crystallization temperature of the pre-cursor glass shift towards the higher temperature. The crystallization behavior that occurred during the heat treatment procedure leads to the enhancement of dielectric constant. All the three compositions of glass-ceramic composites exhibit ferroelectricity when tested at room tem-perature. Both the values of the remanent polarization and coercive field are enhanced regularly with the gradual increase in the concentration of Gd2O3 additive under the same testing field.