等离子喷涂Cr2 03 -8% Ti02涂层参数优化研究

等离子喷涂陶瓷涂层与基体的结合强度往往较小,限制了其实际应用,为了提高结合强度,用正交试验方法研究了等离子喷涂工艺的4个主要参数（喷涂距离、电流、主气流量和辅气流量）对Cr2 03 -8% TiO2涂层结合强度的影响,确定了优化工艺并进行了验证试验,比较了工艺优化前后涂层的结合强度、孔隙率和显微硬度。结果表明：影响涂层结合强度的因素主次顺序是喷涂距离、电流、辅气流量、主气流量,工艺优化后能显著提高Cr2 03一8 % TiO2涂层的性能,优化工艺喷涂的Cr2 03 -8% Ti02涂层结合强度达到29. 2MPa,孔隙率为3.80%,显微硬度为2 528HV。     

铝合金表面等离子喷涂Al2O3-3%TiO2复合涂层工艺参数优化的研究

目的 通过优化等离子喷涂工艺参数，提高铝合金表面等离子喷涂Al2O3-3%TiO2复合陶瓷涂层的结合强度和涂层表截面硬度。方法 用正交试验法，对影响喷涂涂层结合强度和硬度的4个关键喷涂参数进行优化，分别得到喷涂粘结底层Ni-5Al和工作表层Al2O3-3%TiO2的最佳优化参数。结果 通过正交试验确定影响Ni-5Al涂层综合指标的因素由主到次是喷涂电流、喷涂距离、辅气流量、主气流量，最优水平数为2、3、2、1；影响Al2O3-3%TiO2涂层综合指标的因素由主到次是喷距、辅气流量、电流、主气流量，最优水平数为2、3、2、1。Ni-5Al涂层的最佳喷涂工艺参数为：喷涂距离120 mm，喷涂电流520 A，主气流量42 L/min，辅气流量7.5 L/min。Al2O3-3%TiO2复合涂层最佳喷涂工艺参数为：喷涂距离90 mm，喷涂电流530 A，主气流量46 L/min，辅气流量7.8 L/min。最佳工艺下制备的Ni-5Al底层与基体的结合强度为25.2 MPa，Al2O3-3%TiO2复合涂层与Ni-5Al底层的结合强度为17.8 MPa，且其截面硬度在1000HV0.5以上。结论 对喷涂工艺参数进行优化可以得到质量高且稳定的Al2O3-3%TiO2复合喷涂涂层，与非最佳工艺参数喷涂涂层相比，各指标均有较大提高。     

超音速等离子喷涂工艺对纳米Al_2O_3-13%TiO_2涂层的影响

采用四因素三水平正交试验,通过显微硬度和孔隙率两项指标的评估,对超音速等离子喷涂电流、电压、Ar气流量和喷涂距离4个工艺参数进行了优化设计。结果表明,4个因素对纳米Al2O3-13%TiO2涂层综合性能的影响主次顺序是:喷涂电压、Ar气流量、喷涂距离、喷涂电流,并最终确定了最优的喷涂参数。利用XRD、SEM等手段分析了纳米Al2O3-13%TiO2复合粉末和涂层的相结构和微观结构,采用显微硬度计和图像处理方法测定了涂层的显微硬度和孔隙率。最优工艺参数制备的涂层显微硬度值1208 HV,孔隙率为2.26%,拉伸法测定其结合强度为48 MPa。     

基于遗传神经网络的等离子喷涂纳米ZrO2-7%Y2O3涂层工艺参数优化

将BP神经网络和遗传算法相结合用于等离子喷涂纳米ZrO2-7％ Y2O3涂层的工艺参数优化,根据正交试验结果对模型结构进行训练,建立了喷涂距离、喷涂电流、主气压力、辅气压力与涂层结合强度和显微硬度之间的BP神经网络模型,并基于遗传算法对涂层结合强度和显微硬度进行了单目标和多目标参数优化.结果表明,模型预测值与试验值十分接近,说明该网络模型是正确和可靠的.遗传算法优化的涂层最大结合强度和显微硬度(HV)分别为44.0 MPa和12.663 GPa;当涂层结合强度和显微硬度两个性能参数权重相同时,在喷涂距离90.66 mm、喷涂电流934.63 A、主气压力0.304MPa和辅气压力0.898 MPa时涂层综合性能最优.     

等离子喷涂纳米Al2O3-13%TiO2陶瓷涂层的工艺研究

采用正交实验方法对等离子喷涂纳米Al2O3-13%TiO2陶瓷涂层的电压、电流及主气流量进行优化设计,并利用SEM、XRD对纳米Al2O3-13%TiO2复合粉和涂层进行检测和分析.结果表明,影响涂层热震性能的因素主次关系是电流>电压>主气流量;优化后的喷涂参数为电压60V,电流450A,主气流量40L/min,优化后纳米涂层的熔融、涂覆状态有所改善.喷涂时涂层中生成了γ-Al2O3,增加了涂层内的孔隙率,同时,Rutile-TiO2相转变成Brookite-TiO2相,增加了涂层中的内应力,加剧了裂纹的扩展,降低了涂层的抗热震性能.     

等离子喷涂NiCrAl涂层工艺优化研究

采用Metcod43NS(成分NiCrAl)粉末和PARXAIR-5710等离子喷涂系统制备NiCrAl涂层,为了使Ni-CrAl等离子喷涂涂层获得优良的涂层性能,选择涂层结合强度为判据,通过正交试验对NiCrAl等离子喷涂工艺进行了优化。利用扫描电镜,Axio Imager.A 1 m金相图像分析系统等手段对涂层界面形貌和孔隙率进行分析,同时对涂层的结合强度以及显微硬度进行测试。确定优化后的喷涂工艺参数为:喷涂电流为700 A,喷涂距离140 mm,主气流量56.6 L/min,辅气流量28.3 L/min。研究结果表明,喷涂电流、喷涂距离、主气流量、辅气流量对NiCrAl涂层结合强度具有不同的影响,在优化的喷涂工艺参数条件下,NiCrAl涂层结合强度为59.23 MPa,显微硬度为268HV,孔隙率为4.97%。     

等离子喷涂AlSi-ployester封严涂层工艺优化研究

采用AlSi-ployester粉末和PARXAIR-3710等离子喷涂系统制备封严涂层.为使AlSi-ployester等离子喷涂涂层获得优良的涂层性能,选择涂层结合强度为判据,通过正交试验对AlSi-ployester等离子喷涂工艺进行了优化.利用扫描电镜,Axio lmager.A lm金相图像分析系统等手段对涂层形貌和孔隙率进行分析,同时对涂层的硬度、抗热震性能进行了测试.确定优化后的工艺参数为:电弧电流790A.主气流量62.7 L/min,辅气流量5 L/min,喷涂距离100mm.结果表明,电弧电流、主气流量、辅气流量、喷涂距离对AlSi-ployester涂层结合强度具有不同的影响,在优化的喷涂工艺参数条件下,AlSi-ployester涂层结合强度可达6.9MPa,具有较好的硬度和热震性能,可为今后等离子喷涂系统工艺参数的选定提供参考.     

CuNiCoBe合金表面等离子弧喷涂Cr3C2-NiCr涂层

利用等离子弧喷涂技术在结晶器CuNiCoBe基体上制备了Cr3C2-NiCr涂层,采用正交试验法研究了喷涂工艺参数对涂层与基体结合强度的影响,对拉伸断面的形貌和涂层的显微结构进行了观察和分析.结果表明,影响Cr3C2-NiCr涂层与CuNiCoBe基体结合强度的主次因素依次为:送粉速率＞主气流量＞喷涂距离＞喷涂功率;经正交试验优化后的喷涂工艺参数为:喷涂距离90mm,主气流量56.6L/min,送粉速率20 g/min,喷涂功率25 kW;优化后,涂层与基体的结合强度可达18.5 MPa;涂层截面的显微硬度分布符合正态分布.     

球扁钢用铸铁轧辊表面等离子喷涂Cr3C2-25NiCr涂层工艺优化

以球扁钢轧制用铸铁轧辊的表面强化为目的,对等离子喷涂Cr3C2-25NiCr涂层工艺进行了研究.结果表明,影响涂层强度的因素依次为功率、喷涂距离、主气流量和送粉速率,Cr3C2-25NiCr涂层最佳工艺参数是喷涂距离130 mm,主气流量69.8 L/min-1,送粉速率25 g/min,功率20 kW.采用优化后的等离子喷涂工艺制备的涂层,呈典型的层状结构,粒子熔化充分,组织致密,孔隙率低,与基体结合较紧密.     

超音速等离子转移弧喷涂铝涂层的响应曲面法工艺优化

采用超音速等离子转移弧喷涂铝涂层,通过响应曲面法中的 Box-Behnken 中心组合试验设计了三因素三水平的工艺优化试验,建立了主气流量、工作电流和喷涂距离与涂层孔隙率之间的数学模型。 对最优工艺参数条件下制备的铝涂层,利用 SEM、XRD 对涂层的微观形貌和组织成分进行表征;利用 HMV-2000 型维氏硬度计和 MTS 809 万能拉伸试验机对涂层的显微硬度和结合强度进行测试分析。 结果表明:随着主气流量增大、工作电流减小或者主气流量减小、 工作电流增大,孔隙率均呈减小趋势,得到的最优喷涂工艺为:主气流量:100 L/ min,工作电流:200 A,喷涂距离: 100 mm,丝与喷嘴的距离:10 mm,送丝速度:6 m/ min。 通过最优工艺制备的铝涂层,涂层致密,孔隙率为 2. 3%;涂层与基体的结合强度较高为 24. 4 MPa,显微硬度为 44. 5 HV_{0. 1} 。     

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.     

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.     

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⁺.