Al2O3–TiB2复合陶瓷涂层制备及耐液锌腐蚀性能

针对连续热镀锌生产线中浸锌零部件表面的腐蚀磨损问题,应用高能高速等离子喷涂设备制备了Al2O3-TiB2复合陶瓷涂层。测试了涂层的显微组织、显微硬度、结合强度及耐熔融锌液腐蚀性能。结果表明涂层显微组织中不存在相互贯通的孔隙、微裂纹和未熔化颗粒,孔隙分布均匀且孔径较小,孔隙率<3%。涂层与基体结合状态良好,结合强度达到56 MPa。经过30天的熔融锌液浸泡,涂层表面未见有点蚀、裂纹或剥落现象。Al2O3-TiB2复合陶瓷涂层高的致密性和较好的抗热震性能对涂层力学性能和耐熔融锌液腐蚀性能提高起到了重要作用。     

溶胶-凝胶法45钢表面制备Al2O3陶瓷涂层及性能

采用溶胶-凝胶法在45钢表面制备了Al2O3陶瓷涂层,研究了通过化学镀Ni-P层为中间过渡层对45钢表面Al2O3陶瓷涂层性能的影响.通过压入法和划痕法研究了膜基结合强度,观察了复合涂层压痕和划痕形貌,通过扫描电子显微镜(SEM)对复合涂层表面形貌进行了分析.结果表明,中间层与基体材料、Al2O3层与中间层结合良好,涂层均匀致密,表面显微硬度最大值为1030HV,压入法结果表明膜与45钢基体结合较好.     

镁合金表面等离子喷涂Al2O3-TiO2陶瓷涂层的耐腐蚀性研究

采用等离子喷涂技术在AZ31镁合金表面制备Al2O3-13％TiO2陶瓷复合涂层,对涂层的微观组织进行了观察分析,测试了涂层的表面硬度.通过极化曲线和浸泡腐蚀试验,对比研究了镁合金基材及喷涂陶瓷涂层的试样在5％ NaCl溶液中的耐腐蚀性能.结果表明:涂层镁合金试样的硬度和耐腐蚀性优于基体镁合金,但当腐蚀液透过涂层孔隙时...     

反应喷涂制备Al2O3-TiB2复相涂层的工艺研究

利用反应喷涂方法在铝合金表面制备Al2 O3-TiB2复相涂层,分析了机械合金化、喷涂温度以及添加粘结剂等工艺对涂层组织形貌的影响,得出了制备涂层较理想的工艺方法,并测试了涂层的显微硬度.结果表明:球磨后的混合粉末添加过量Al粘结剂,经过等离子喷涂可以制得Al2 O3-TiB2复相涂层,涂层组织形貌良好,致密度高,其显...     

沉没辊基础件的熔融锌液腐蚀研究现状

根据近些年国内外耐锌腐蚀的研究成果,将耐锌腐蚀方法分为两大类:自身耐锌腐蚀材料和表面改性处理。自身耐锌腐蚀材料主要集中在Fe-Cr-Mn、Fe-B、Ti Al Nb等材料上,表面处理主要集中在WC-Co、Mo B-Co Cr、陶瓷等涂层上。两种方法都获得一定的研究成果,但也有一些不足。自身耐锌腐蚀材料的耐熔锌腐蚀虽有改善,但在液锌中也只是延缓了腐蚀速度,最终仍然会腐蚀失效。表面涂层耐蚀性相对较好,但是在锌液中仍然会发生裂纹腐蚀,并且涂层和基体之间的物理匹配性较差,脆性较大,工件的轻微碰撞很容易造成涂层的脱落,加速工件的腐蚀,不宜用于实际生产。充分利用陶瓷耐腐蚀、耐高温、硬度高的优点,以及金属室温强度好、延展性好的优点,开发陶瓷金属复合涂层,可能会成为下一步沉没辊基础件熔融锌液腐蚀研究的主要方向。     

Al_2O_3含量对Al_2O_3-Al复合涂层组织和摩擦磨损性能的影响

通过改变喷涂粉末中Al2O3和Al的比例,在AZ91D镁合金表面制备不同Al2O3含量的等离子喷涂Al2O3-Al复合涂层。对复合涂层的显微组织、硬度和摩擦磨损性能进行表征,研究Al2O3含量对涂层组织和磨损性能的影响。结果表明,涂层组织为带状Al2O3分布在致密的Al基体上,Al2O3内可见细微的片层结构,且层与层间存在一定的孔隙。复合涂层中Al平均硬度62HV,Al2O3平均硬度达1380 HV。摩擦磨损实验证实,复合涂层具有较小的摩擦系数和较低磨损量,大大改善了镁合金表面的抗磨损性能。涂层中Al2O3体积少于Al时,Al2O3增加使涂层的抗磨效果增强。涂层中Al2O3体积超过Al后,涂层的孔隙增多、涂层变脆,其耐磨损性能下降。     

等离子喷涂Cr2O3/TiO2高温氧化物陶瓷 复合涂层的微观组织及电化学性能

目的 通过等离子喷涂工艺,在油气管道X70管线钢表面制备出Cr2O3/TiO2高温氧化物陶瓷复合涂层,研究该涂层的微观组织与电化学性能。方法 采用9MC Plasma Control Unit等离子喷涂系统,基于线切割尺寸为40 mm×24 mm×6 mm的X70管线钢基体表面,沉积Cr2O3/TiO2高温氧化物陶瓷复合涂层。利用金相显微镜和扫描电子显微镜观察该复合涂层的微观组织与形貌,利用X射线衍射仪分析该复合涂层的物相组成,利用电化学工作站测定该复合涂层的电化学腐蚀性能。结果 Cr2O3/TiO2高温氧化物陶瓷复合涂层由完全熔化区和半熔化区双态组成,呈典型的等离子喷涂层状结构,层与层之间结合较紧密,分布着富Cr2O3沉积区与富TiO2沉积区,无相变产生,完全熔融的TiO2液相可嵌入到未完全熔融的Cr2O3结构间隙中形成固溶结构。经电化学腐蚀性能测试,其自腐蚀电位介于-0.4 ~ -0.3 V之间,高于X70管线钢基体的自腐蚀电位-0.6 ~ -0.5 V,腐蚀倾向滞后,表现出好的抗腐蚀性能。结论 研究选取的等离子喷涂参数较合适,并成功制备出了能明显提高油气管道X70管线钢抗电化学腐蚀性且组织分布均匀的Cr2O3/TiO2高温氧化物陶瓷复合涂层。     

热喷涂NiCr／纳米（ZrO2＋8％Y2O3）梯度涂层的性能研究

针对陶瓷涂层与基体结合强度低、易产生裂纹和剥落的现象,进行了抗高温氧化耐磨损梯度涂层的设计.采用热喷涂技术在45钢基体表面制备由面层[纳米(ZrO2 8%Y2O3)]和中间层(NiCr)组成的梯度涂层,利用扫描电镜(SEM)、测定结合强度、测定显微硬度、X射线衍射等方法研究涂层的性能.结果表明:NiCr/纳米(ZrO2 8%Y2O3)梯度涂层显微组织结构致密,与NiCr合金涂层和纳米(ZrO2 8%Y2O3)陶瓷涂层相比,具有更优良的力学性能;梯度涂层的面层有利于提高基体的耐高温、耐磨损性能,而中间层则有利于改善基体的抗高温氧化性能.     

激光熔覆等离子喷涂Al2O3陶瓷涂层组织结构研究

研究了45钢表面激光熔覆等离子喷涂Al2O3陶瓷涂层的组织结构、显微硬度及滑动磨损特性.结果表明,等离子喷涂Al2O3涂层的组织呈层片状,层间为机械结合,涂层由α-Al2O3, ZrO2和少量γ-Al2O3组成;激光熔覆Al2O3陶瓷涂层组织为细小枝状晶,由α-Al2O3及少量ZrO2组成.激光熔覆Al2O3涂层的显微硬度较高,滑动磨损时耐磨性明显优于等离子Al2O3喷涂层.     

溶胶-凝胶法制备Al2O3·ZrO2复合陶瓷涂层研究

用溶胶-凝胶(Sol-gel)法以Al(NO3)3·9H2O,ZrOCl2·8H2O为原料,乙醇为溶剂,在不锈钢表面制备了xAl2O3·yZrO2复合陶瓷涂层.研究了基材氧化预处理、溶液纽成、添加剂等对陶瓷涂层组成、性能的影响.结果表明:基材氧化预处理能大大改善涂层与基材的结合强度:涂有xAl2O3·yZrO2陶瓷涂层的材料具有较不锈钢更优良的抗高温氧化性能.     

Fe-15Ce合金在H2-CO2、H2-H2S及H2-H2S-CO2气氛下的腐蚀

研究了600℃时Fe-15Ce合金在H2-CO2、H2-H2S及H2-H2S-CO2 3种气氛中的腐蚀行为，Fe-15Ce合金腐蚀后发生了Ce的内氧化或形成了复杂的腐蚀产物膜，而未出现Ce的选择性氧化或硫化，这主要是合金中存在着两相及Ce在Fe中极低的溶解度的结果。Fe-15Ce合金在本实验条件下的氧化-硫化腐蚀速度低于相同温度、压力下的纯硫化。     

用氢-氧取代氧-乙炔作焊接切割的必要性及可行性

阐述了用氢代乙炔的必要性．通过时HGQU2000／315火焰电孤焊割机的考察和试用证实了用氢代乙炔的可行性，比较了两种气体的性质并提出了使用特性差异和注意事项．提出了进一步探索的问题。     

Thermodynamics and phase diagrams in the binary systems Na2O-SiO2, Na2O-GeO2, Na2O-B2O3, Li2O-B2O3, CaO-B2O3, SrO-B2O3, and BaO-B2O3

We applied our model to the enthalpy of mixing data of the binary systems Na₂O-SiO₂, Na₂O-GeO₂, Na₂O-B₂O₃, Li₂O-B₂O₃, CaO-B₂O₃, SrO-B₂O₃, and BaO-B₂O₃. The most stable composition in the liquid, that is where the enthalpy of mixing is most negative, is with a metal-oxygen ratio of 4 to 3, for monovalent metals (Na and Li) and 3 to 4 for divalent metals (Ba and Ca) in liquid silicates or borates. The same applies to the CaO-SiO₂, CaO-Al₂O₃, PbO-B₂O₃, PbO-SiO₂, ZnO-B₂O₃, and ZnO-SiO₂ systems. The oxygen to metal ratio, its constant value in various types of systems, reflects and describes the structure of the liquid. Using the analyzed enthalpies of mixing data and the available phase diagrams, we calculated the enthalpies of formation of the various binary compounds. The results are in excellent agreement with data in the literature that were obtained from direct solid-solid calorimetry.     

IrO2-MnO2中间层Ti/RuO2-TiO2-SnO2电极制备及性能

通过热分解法制备了含IrO2-MnO2中间层Ti/RuO2-TiO2-SnO2电极,采用SEM、EDX、XRD、CV等检测方法对中间层进行表征,同时采用强化加速寿命试验对电极电化学稳定性进行表征。结果表明:450℃时前躯体完全氧化并形成固溶体,制备的中间层晶粒细小,表面结构致密,电化学孔隙率小。添加中间层使Ti/RuO2-TiO2-SnO2电极强化寿命由未加中间层的7.5h提高到995.8h,远高于国家标准20h。     

ACTIVITY OF La_2O_3 IN LIQUID La_2O_3-CaF_2 AND La_2O_3-CaF_2-CaO-SiO_2 SLAGS

用石墨为还原剂,将渣中La_2O_3还原入液态Sn,以测定1500℃下La_2O_3-CaF_2和La_2O_3-CaF_2-CaO-SiO_2渣中La_2O_3的活度.对La_2O_3-CaF_2系,并用Gibbs-Duhem积分法求得CaF_2的活度. 根据液态渣的离子结构模型,对上述二渣系中La_2O_3的活度数据进行了简单的讨论.     

Mechanoluminescence in BaSi2O2N2:Eu

Mechanoluminescence (ML), a general term for the phenomenon in which light emission occurs during any mechanical action on a solid, can be divided roughly into two classes: destructive ML and non-destructive ML. For practical use in high-end applications (e.g. pressure sensors), materials with non-destructive ML properties are preferred. This paper reports on the strong non-destructive ML in BaSi₂O₂N₂:Eu. When irradiated in advance with ultraviolet or blue light, this phosphor shows intense blue-green light emission upon mechanical stimulation such as friction or pressure. The ML has an emission band peaking at 498 nm, which is ～4 nm red-shifted compared to the steady-state photoluminescence. The origin of the ML is discussed and related to the persistent luminescence of BaSi₂O₂N₂:Eu. The same traps are responsible for both phenomena. Based on the occurrence of ML in this phosphor, we were able to show that the predominant crystallographic structure of BaSi₂O₂N₂:Eu belongs to space group Cmc2₁.     

氢分子在贮氢材料Li2MgN2H2表面的吸附与解离

采用第一性原理计算方法研究了Li-Mg-N-H体系贮氢材料的放氢产物Li2MgN2H2的吸氢反应过程中的过渡态、表面电子态密度和表面能。结果表明:氢分子在Li2MgN2H2低指数表面中最低能量(100)表面的Mg-Mg-Li穴位吸附位置能够形成最稳定的吸附结构并发生解离,氢分子吸附能为-0.1898eV,解离能约为0.84eV(81kJ/mol),表明该反应所需的反应活化能仍较高,吸氢反应速度缓慢。     

Thermodynamic evaluation of phase equilibria in the CaCl2-MgCl2-CaF2-MgF2 system

The phase diagram of the CaCl₂-CaF₂-MgCl₂-MgF₂ reciprocal ternary system was calculated thermodynamically from available data on the common-ion binary subsystems and from available data on the CaCl₂-MgF₂ join. This join is very nearly quasibinary and divides the system into two quasiternary systems: the CaCl₂-MgF₂-CaF₂ system with a ternary eutectic calculated at 724 +-5 °C and the CaC₂-MgF₂-MgCl₂ system with a ternary eutectic calculated at 561 +-5 °C.     

High temperature corrosion of Fe-Cr-Mn-alloys in H2-H2S and H2-H2O-H2S gas mixtures

The sulfidation of Fe-20% Cr-30% Mn, Fe-25%Cr-20%Mn and Fe-25% Cr was studied at 700°C in H₂-H₂S and the oxidation and sulfidation in H₂-H₂O-H₂S after preoxidation in H₂-H₂O. The sulfidation rate is strongly increased for the Mn-containing alloys, layers of (Mn,Cr)S and (Mn,Fe)Cr₂S₄ are formed. Also the oxidation rate is enhanced compared to Fe-25% Cr by formation of MnCr₂O₄ instead of Cr₂O₃. The sulfidation after preoxidation leads to internal and external sulfidation of the Mn-containing alloys. With increasing oxygen pressure p(O₂) = 10^?26…10^?22 atm. of the H₂-H₂O-H₂S mixtures the sulfidation is suppressed, for the higher oxygen pressure 10^?23 and 10^?22 atm. fast oxidation prevails under formation of MnCr₂O₄. Manganese cannot increase the sulfidation resistance of alloys, in spite of the stability and low degree of disorder of its sulfide, since the mixed sulfide (Mn,Cr)S is formed which has a high degree of disorder, high diffusivities and high growth rate according to the doping effect of trivalent Cr³⁺.     

The Quasi-Ternary System Cu2Se-Ga2Se3-GeSe2

The quasi-ternary system Cu₂Se-Ga₂Se₃-GeSe₂ was investigated using the methods of differential thermal and x-ray analysis. An isothermal section at 770 K and a liquidus surface projection of the phase diagram were constructed. The existence of the quaternary phase CuGaGeSe₄, the boundaries of solid solutions ranges of the system compounds were established.