时效Ag-7wt.%Cu合金的微观组织、电阻率和硬度

采用差示扫描量热法、X射线衍射及透射电子显微镜研究了固溶和固溶一冷轧Ag-7wt.%Cu合金在时效过程中富Cu相的析出动力学和形貌特征,同时结合电阻率和显微硬度的测量,定量对比了固溶和固溶一冷轧Ag-7wt.%Cu合金时效过程中富Cu相对电阻率和硬度的影响及其机理.研究结果表明:固溶样品中富Cu相反应温度为300℃-350℃,析出激活能为(111±1.6)kJ/mol;而固溶一冷轧样品中由于形变能的存在,富Cu相温度降低为290℃-330℃,析出激活能升高为(128±12)kJ/mol.XRD结果证实富Cu相的析出过程与时效温度有关.固溶和固溶一冷轧合金在450℃时效后均能观察到球状的富Cu相,富Cu相的析出和溶解过程对电阻率和显微硬度有显著影响.当时效温度低于450℃时,随时效温度的提高,固溶一时效样品的电阻率降低,显微硬度增加:而固溶一冷轧一时效样品的电阻率和显微硬度均逐渐降低.显微硬度除了受富Cu相的影响外,还受到位错和形变孪晶的影响.当时效温度高于450℃时,两种样品的电阻率增大,而显微硬度降低.     

静磁场复合电流下时效对Cu—Cr—Zr合金组织及性能的影响

本文在经过固溶和冷变形处理Cu—Cr-Zr合金的等温时效过程中同时施加电流密度为100A／cm2的直流电流和不同磁感应强度的静磁场,发现电磁复合场能显著影响Cu—Cr-Zr合金的组织及性能．和无磁场下时效后合金性能相比,施加磁场后的合金电导率和显微硬度值均有一定程度的升高,其中在350℃,10T磁场下效果最明显,分别升高了22．1％IACS和25．3HV．利用透射电镜观察显微组织观察发现,施加磁场后合金组织中位错密度有所降低,同时出现了大量细小弥散的铬析出物,表明电磁复合场能进一步促进铜合金的时效过程,在低温时效时尤其明显．分析认为,电磁复合场对Cu-Cr-Zr合金时效过程的促进作用机理是磁场增强了电流的“电子风”效应．     

Al-4.5wt%Cu合金中溶质原子及析出相对锯齿形屈服时空特性的影响

借助不同温度下的固溶处理，得到一系列具有不同溶质原子浓度及析出相含量的Al-4.5wt%Cu合金材料试件.比较这些试件在拉伸实验中的锯齿形屈服现象的时空特性，分析溶质原子与析出相对位错运动的影响，从而探究动态应变时效产生的微观机理.实验结果显示，当固溶处理温度由500℃逐步降低，应力-时间曲线上的应力锯齿跌落幅值逐渐减小，并在300℃时达到最小.继续降低固溶处理温度至100℃，应力锯齿跌落幅值又逐渐增大.同时，热处理方式的改变对剪切带的传播特性也有显著影响.实验发现，固溶处理温度高于300℃时，溶质原子对DSA的影响强于析出相；反之，固溶处理温度低于300℃时，析出相对DSA的影响强于溶质原子；室温下析出相是影响Al-4.5wt%Cu合金DSA机理的主要因素. 关键词： 铝铜合金 锯齿形屈服 动态应变时效 固溶处理     

钛合金表面激光熔覆TiC_p/Ni基合金复合耐磨涂层

采用激光熔覆技术在TC4合金表面制备TiC颗粒增强的Ni基合金复合材料涂层,测试了熔覆层的硬度和滑动摩擦磨损性能,分析了熔覆层的强化机制。结果表明,熔覆层中存在颗粒强化、固溶强化和细晶强化等多种强化作用,熔覆层的显微硬度达HV900～1100,耐磨性能比TC4合金显著提高。     

Ca、Sr对汽车用镁合金组织与力学性能的影响

以Mg-Al-Mn合金为研究对象,通过微合金化的方法研究了Ca、Sr对汽车用耐热镁合金常温力学性能与高温力学性能的影响,并分析了合金在固溶时效热处理后的时效硬化特征,观察了合金铸态、固溶态和时效态下的显微组织演变。     

时效时间对FeNiAlTa形状记忆合金组织结构和性能的影响

本文以 Fe_59.5Ni₂₈Al_11.5Ta₁ 形状记忆合金为研究对象, 采用金相显微镜、X 射线衍射仪、扫描电镜、能谱仪和压力试验机等研究了轧制后不同时 效时间处理对该合金组织结构和性能的影响. 结果表明, 随着时效的进行, γ’ 相和 β’ 相的相继析出, 强化了奥氏体基体. 综合伪弹性曲线看出, 随着时效时间的增加, 600 ℃时效态合金的应力诱发马氏体临界应力先减小后增大, 合金的抗压强度、可恢复的应变和硬度都先增大后减小, 合金的残余应变则先减小后增大, 时效时间为 60 h 时, 合金的抗压强度最大, 到达1306 MPa, 此时合金的可恢复形变最大, 达到14.9%, 合金的硬度也最大, 合金的残余应变相对最小. 但随着时效时间的延长, 合金的最大应变逐渐减小, 合金塑性逐渐减小. Fe_59.5Ni₂₈Al_11.5Ta₁ 形状记忆合金的性能与沉淀相的颗粒大小、分布、体积分数等因素有关. 关键词： 59.5Ni₂₈Al_11.5Ta₁')" href="#">Fe_59.5Ni₂₈Al_11.5Ta₁ 时效处理 伪弹性 硬度     

Nb-Ti超导合金中ω相及其对临界电流密度的影响

用高压透射电镜对时效Nb-Ti合金的析出相类型和形态及其对临界电流密度的影响进行了研究.在Nb-65％Ti合金中,高温淬火后350℃时效观察到ω相的大量析出,其大小为100—300A,ω相的析出明显地提高合金的临界电流密度和硬度.在Nb-65％Ti和Nb-50％Ti合金中,450℃时效观察到存在二种析出相——ω相和α相.α相呈粗大针状,同时合金的J_c和H_r值显著降低.     

微激光冲击DZ17G合金的表面完整性影响研究

为了在不影响柱状晶组织的前提下改善DZ17G定向凝固合金的力学性能,采用微激光冲击强化方法进行表面处理,通过X射线衍射、扫描电子显微镜、透射电子显微镜和显微硬度计,测试分析微激光冲击对DZ17G定向凝固合金表面完整性的影响。试验结果表明:在水下无吸收保护层微激光冲击处理后,合金表面发生了烧蚀、熔融,1次冲击后形成光滑熔融区,但随着冲击次数增加而形成了大量微小烧蚀孔洞和难熔颗粒;表层组织仍由和两相组成,柱状晶内形成了高密度位错和位错缠结,但未发生晶粒细化;硬度在深度上呈梯度分布,冲击1次后硬化层深度仅为100 m,表面硬度值达到503 HV,提高了22.7%,而且硬度值和硬化层深度都随着冲击次数增加而增大。     

时效工艺对PtCo合金磁性能的影响

研究了时效温度对PtCo合金磁性能的影响.磁性能测量结果显示,随着时效温度的增加合金的剩磁逐渐减小,时效温度为690 ℃时,合金的矫顽力达到最大值.第一步时效处理后,合金的有序度S随时效温度的提高而增加,长程有序度的增加说明合金有序相的晶粒尺寸也在增加,这是合金矫顽力变化的根本原因.第二步时效处理后,PtCo合金的微观组织结构不发生改变,有序相的各向异性场增大,使合金的矫顽力增大. 关键词： 时效温度 PtCo合金 磁性能 有序度     

高耐磨化学共沉积复合材料的组成与耐磨性能研究

采用化学沉积方法，制备镍合金－碳化硅，氧化铝，金刚石复合材料，研究了金属基体与硬质非金属粒子复合材料的组成与耐磨性能，硬质粒子相随着镍合金的还原反应沉积而复合，二者复合界面不产生反应系机械结合；随着硬质粒子相添加量的提高，复合材料晶化倾向加大，与镍合金相比，复合材料的硬度和耐磨性能显著上升，金刚石复合材料为最高；经过４００℃时效处理，复合材料基体析出磷化物Ｎｉ３Ｐ，进一步得以强化，表现为硬度升高，     

Effect of heat treatment on the mechanical and microstructural characterization of Mg-AZ91E/TiC composites

Mg-AZ91E/TiC_p composite was fabricated using a spontaneous infiltration technique at 950 °C under an argon atmosphere. The composites produced have 37 vol.% of metal matrix and 63 vol.% of TiC-like reinforcement. The obtained composites were subsequently solution heat-treated at 413 °C during 24 h, cold water quenched, and subsequently artificially aged at 168 and 216 °C during 16 h in an argon atmosphere. Effect of heat treatment on the microstructure and mechanical properties was evaluated. Microstructural characterization was analyzed using different techniques such as X-ray diffraction (XRD) and scanning electron microscopy (SEM). Interface between matrix and reinforcement was examined using transmission electron microscopy (TEM), and mechanical properties were evaluated by measuring the elastic modulus and hardness. Mg, TiC, Al, and Mg₁₇Al₁₂ phases through XRD were detected. Meanwhile, using TEM analysis in heat-treated composites MgAl₂O₄, MgO, and Al₂O₃ were identified. The as-fabricated composite have elastic modulus and hardness of 162 GPa and 316 Hv, respectively. After solution heat treatment and aging at 168 °C during 12 h, the composites reaches values of 178 GPa and 362 Hv for the elastic modulus and hardness, respectively. Time of aging was correlated with measures of elastic modulus and hardness.     

Preparation of poly(2-ethyl aniline)/kaolinite composite materials and investigation of their properties

Conductive poly(2-ethyl aniline) (PEAn)/kaolinite composite was prepared by chemical polymerization in aqueous HCl medium in the presence of kaolinite particles by using potassium chromate (K₂CrO₄) as oxidant. Effects of polymerization conditions, such as concentrations of oxidant and 2-ethyl aniline, polymerization time and temperature on PEAn content and conductivity of composite, were investigated. The prepared composite material, having the highest PEAn content and conductivity, was obtained in the polymerization carried out at 20 °C for 2 h with 0.2 M K₂CrO₄ and 0.2 M EAn. It was observed that the micro-hardness of prepared composites increased with the increase in the PEAn contents of composites. The highest micro-hardness value of 7.92 kg mm⁻² was reached at 24.6% PEAn content. Characterization of composites was carried out by FTIR spectroscopy, XRD, TGA and SEM techniques.     

Synthesis of nanocrystalline SnO<Subscript>2</Subscript> in supercritical water

Nanocrystalline SnO₂ was synthesized in supercritical water at 385–415°C and 30 MPa (38–106 s residence time) in a tubular flow reactor from an aqueous solution of 0.1–0.4 M SnCl₄. The conversion rate was between 53 and 81%, but increased to 97.8% when 0.1 M NaOH was added. Nanoparticles were analyzed by a series of independent analytical techniques, including TEM, Raman, XRD, SEM, EDX and FT-IR. The initial size of the particles was about 3.7 nm. After calcination at 450°C for 2 h, the particle size increased to 4 nm. The particles were of low crystallinity, as indicated by the weak Raman and XRD signals. All particles were composed of Sn and O, as verified by the EDX spectra. The crystals were tetragonal, as confirmed by the weak XRD spectrum. After calcination at 600°C for 10 h, the particle size increased to 9 nm, while high crystallinity was confirmed by Raman and XRD analyses. All the crystals had the same structure, as indicated by TEM electron diffraction patterns. Using this one-step supercritical water process, nanoparticles of SnO₂ can be conveniently produced continuously in a flow reactor in less than 2 min.     

氧化锌纳米棒的生长过程研究

利用高分子聚乙烯吡咯烷酮(PVP)和乙酸锌的配合物作为前驱体,在300 ℃温度下煅烧,并制备了氧化锌纳米棒。生成的产物用XRD,TEM,SAED等测试方法进行了表征。为了研究氧化锌纳米棒的生长过程,我们通过控制制备前驱体所需原料的比例不变,改变在300 ℃温度下煅烧的时间,分别为0.5, 3, 12和24 h,来观察生成产物的形貌特征。实验发现在110 ℃温度下干燥的前驱体中已经有氧化锌微晶生成;在300 ℃温度下煅烧0.5 h后就出现了明显的由几个纳米大小的微晶所组成的氧化锌纳米棒;煅烧3 h后的产物是结构非常完整的径直单晶ZnO纳米棒;12和24 h煅烧前驱体生成的ZnO纳米棒长度有所增加,ZnO的量基本保持不变。实验发现氧化锌的生长是沿着c轴方向,但是在横向也有生长方向。     

Gd2O3:Eu纳米晶的制备及其光谱性质研究

以EDTA为络合剂，聚乙二醇为有机分散剂，用络合溶胶—凝胶法制备出Gd2O3:Eu纳米晶。用XRD，SEM，X—射线能量色散谱仪(EDS)，荧光分光光度计等分析手段对Gd2O3:Eu的纳米晶结构、形貌、组分的均匀性以及发光特性进行了研究。结果表明：EDTA—M凝胶仅在800℃焙烧即可得到颗粒细小、组分均匀、纯立方相的Gd2O3:Eu纳米晶，颗粒基本呈球形，粒径为30nm左右。对样品的激发光谱、发射光谱测定表明：Gd2O3:Eu纳米晶在269nm光激发下发红光，发射光谱谱峰在611nm，与体材料基本相同；激发光谱中电荷迁移带(CTB)明显红移，从体材料的255nm移至269nm，移动了约14nm；猝灭浓度从体材料的6％提高到8％。     

Effect of ZnAl2O4 coating on the compressive behaviors of aluminum borate whiskers-reinforced aluminum composites at elevated temperatures

Aluminum borate whiskers (ABOw) with or without ZnAl₂O₄ coating reinforced pure aluminum composites (ABOw/Al, ABOw/ZnAl₂O₄/Al) were fabricated by squeeze casting. The effects of ZnAl₂O₄ coating on the compressive behaviors, microstructures, and matrix textures of the composites were investigated at different temperatures and strain rates. The results indicate that the maximum compressive flow stress of the composites almost linearly decreases with the increase in temperature. The maximum compressive flow stress of ABOw/ZnAl₂O₄/Al composite is higher than that of ABOw/Al composite at the same temperature when the strain rate is larger, however, it is reversed when the strain rate is smaller. It is more serious for the fracture of whiskers in ABOw/ZnAl₂O₄/Al composite than that in ABOw/Al composite at the high compressive strain rate. However, the average length of whiskers in ABOw/ZnAl₂O₄/Al composite is larger than that in ABOw/Al composite at the low compressive strain rate. The strong matrix texture in ABOw/ZnAl₂O₄/Al composite appears at the high compressive strain rate, however, it is observed in ABOw/Al composite at the low compressive strain rate.     

The role of process parameters in plasma surface chromising of Ti2AlNb-based alloys

In order to enhance the wear resistance of Ti₂AlNb-based alloy (O-phase), surface chromising was performed by double glow plasma process in this study. The effect of process parameters, such as temperature, time and pressure, on the microstructure, thickness, and micro-hardness of the alloyed layers was investigated. Scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) were employed to analyze the composition distribution and microstructure of the alloy. The results showed that the optimum process parameters were as follows: 970 °C for temperature, 4 h for chromising time, and 30 Pa for pressure. Following the optimization the thickness, microstructure and micro-hardness of the modified layer achieved the designed requirements. The results of tribological tests showed that the friction coefficient of the chromised layer was lower than that of the matrix at the room temperature or 500 °C, and the specific wear rate of samples with plasma chromising at either room temperature or high temperature was decreased markedly.     

Influence of filler type on wet skid resistance of SSBR/BR composites: Effects from roughness and micro-hardness of rubber surface

The wet skid resistance (WSR) of SSBR/BR(solution styrene-butadiene rubber/butadiene rubber) composites filled with carbon black, silica, and nano-diamond partly replacing carbon black or silica, respectively, was measured with a portable British Pendulum Skid Tester (BPST). A dynamic mechanical thermal analyzer was used to obtain the viscoelasticity of the composites. A 3D scanning white-light interfering profilometer was used and the scratch test performed to characterize surface roughness and micro-roughness, respectively, of the composites. WSR of the silica-filled composite was better than that of the carbon black-filled one, and further enhancement of WSR was obtained by replacing silica with nano-diamond. Tan δ of the composites at 0 °C, 10 Hz, and tensile strain of 2% did not show good correlation with WSR. The surface roughness of the composites had effects on WSR. The scratch test indicated that the higher the hardness of the filler in the composite, the higher the micro-hardness and the better the WSR. Therefore, the surface micro-hardness of the composites is an important factor affecting WSR, besides viscoelasticity and surface roughness.     

CaAl2O4:Eu2+,Nd3+纳米粉体的合成与发光性质

采用溶胶-凝胶法制备了CaAlO4：Eu^2＋,Nd^3＋纳米粉体发光材料。利用DTA,TG,XRD,SEM,光谱分析等手段对样品进行了结构和性能分析。实验结果表明,800℃烧结的样品形成已CaAl2O4晶相,样品平均晶粒尺寸为20～40nm,与CaAlO4：Eu^2＋,Nd^3＋粗晶材料相比,样品的发光光谱发生了“蓝移”,热释光峰值向高温移动了96℃,且曲线形状变宽,发光衰减是由初始的快衰减和随后的慢衰减构成,发光余辉时间5h。     

原位法MgB_2-B_4C复相超导体合成及相含量调控研究

以B4C和Mg为原料合成的MgB2-B4C复相超导体具有高的临界电流密度(Jc)和高的超导转变温度(Tc),是一种有潜力的实用MgB2超导材料,其成相机理对复相MgB2超导体的相含量调控和磁通钉扎研究具有重要意义。结合经典烧结理论,研究了B4C-Mg真空固相烧结制备MgB2-B4C复相超导体的超导相形成和晶粒生长过程,给出了B4C-Mg的金斯特林格扩散模型和MgB2晶粒生长过程。通过选择B4C原料粒径,MgB2-B4C复相超导体超导相体积相含量在18%-88%范围可控。相含量88%的MgB2-B4C复相超导体临界转变温度达33.5K,转变宽度1.5K。10 K环境6T外场下电流密度可以达到1×104A/cm2,表明MgB2-B4C复相超导体具有良好的磁通钉扎行为。