注胶修复工艺的耐高温环氧树脂体系工艺性能

针对注胶修复工艺要求,采用差示扫描量热法热分析和流变仪测试三种中温固化配方的耐高温缩水甘油胺型环氧树脂体系的固化特性和化学流变特性,通过对比分析三种配方树脂体系的固化条件和黏度特性,确定MF-4101/ZH110/DMP-30树脂体系为最适宜注胶修复工艺的配方。建立该树脂体系在等温条件下黏度特性曲线的Daul Arrhenius模型和高阶指数拟合模型。结果表明,高阶指数拟合模型的预测精度和适用范围均优于Daul Arrhenius模型,预测黏度与实验结果具有良好的一致性,根据高阶指数拟合模型建立的黏度随温度、时间变化的唯象关系式,可以准确地预报修复树脂体系的工艺窗口。     

电弧喷涂Fe—Cr—Ni管状丝材涂层性能研究

金属管状丝材是热喷涂领域中的一种新型材料.本文对电弧喷涂含稀土元素的Fe—Cr—Ni营状丝材的涂层结合强度、相对耐磨性、显微硬度等机械性能进行了研究,并利用扫描电镜(SEM)、X射线衍射仪及能谱等分析方法研究了涂层的形貌、成分和相组成.     

步兵轻武器新型夜瞄复合荧光材料的性能研究

采用自制的复合荧光粉体和化学载体成分,研制出一种步兵轻武器新型夜瞄复合荧光材料.通过试验分别研究了新材料的发光性能、耐温性能、耐腐蚀性能和耐表面处理性能.试验结果表明,研制的新型夜瞄复合荧光材料发光时间长、亮度高,具有良好的耐温、耐腐蚀性能,不受武器表面处理的影响,可满足步兵轻武器夜间瞄准需求.     

极性基团对环氧树脂基体力学性能及吸水特性的影响

研究了CYD- 128/THPA/DMP- 30 (CTD)、TDE- 85/THPA/DMP- 30(TTD)、CYD- 128/IPDA(CI)与TDE- 85/IPDA (TI)4种环氧树脂基体浇铸体的拉伸、弯曲和耐海水性能,分析了树脂、固化剂类型和分子结构对树脂基体性能的影响.结果表明,使用相同固化剂时,TDE...     

初始和终止库存不为零的生产与库存问题

针对初始库存和终止库存不为零的生产与库存问题,通过适当设置需求量,将其化为初始库存和终止库存为零的问题,以便应用重生性质进行求解。     

聚碳硅烷纤维化学气相交联研究

以环己烯作为反应气氛,对聚碳硅烷(PCS)纤维进行了化学气相交联不熔化处理。与空气不熔化进行对比,研究了不熔化过程中PCS纤维的反应程度及凝胶含量的变化,并进行了元素分析和热重差热分析,初步探讨了PCS纤维环己烯化学气相交联反应的机理。结果表明,在环己烯气氛中,PCS分子结构中Si-H键的反应程度随不熔化温度的提高逐渐增加,相应地,PCS纤维的凝胶含量迅速提高直至不熔。环己烯受热后产生自由基,引发PCS分子中的Si-H和Si-CH3键断裂形成自由基,促进PCS分子间形成Si-CH2-Si结构而实现交联。     

921A钢在海水中腐蚀的力学化学效应

为了研究弹性应力和弹塑性应变对921A船体钢在模拟海水中腐蚀行为的影响,采用自制的载荷-电化学实验装置对921A钢在载荷与腐蚀介质协同作用时的开路电位、动电位极化曲线和电化学阻抗谱等电化学性能进行了测试,并由电化学阻抗谱拟合得到的电荷传递电阻定义载荷下的腐蚀速率修正因子,将实验得到的腐蚀速率修正因子与理论值进行了对比。结果表明:弹性拉应力与弹性压应力对力学化学效应的影响具有对称性。力学化学效应随着弹性应力的增大而增大,随着弹塑性应变的增大先增大后减小。弹塑性应变对力学化学效应的影响远远大于弹性应力的影响。在研究范围内,弹塑性应变引起的腐蚀电位负移量最大为62.6 mV,相应的腐蚀速率修正因子高达4.113,而弹性应力引起的腐蚀电位负移量最大为24.5 mV,相应的腐蚀速率修正因子为1.746。由此可见,应力应变对921A钢在海水中腐蚀行为的影响不容忽视。     

聚(2-甲氧基-5-丁氧基)亚苯基亚乙烯的合成及电性能

本文用对甲氧基苯酚、正溴丁烷、聚甲醛为原料， 经醚化， 双氯甲基化和碱性消除反应， 合成出长链共轭且可溶的聚（２甲氧基５丁氧基）亚苯基亚乙烯，用 Ｉ Ｒ 和１ Ｈ Ｎ Ｍ Ｒ 表征了中间体和聚合物的结构，并测定了聚合物的伏—安特性曲线。     

Synergistic effect of hybrid Himalayan Nettle/Bauhinia-vahlii fibers on physico-mechanical and sliding wear properties of epoxy composites

The cellulosic bast fibers are recognized as a justifiable and biodegradable substitute for producing moderate strength polymer composite materials because of their characteristics of renewability, eco-friendliness, and higher specific strength. Hence the aim of this research work is to fabricate Himalayan bast fibers (Nettle fiber (NF)/bauhinia vahlii fiber (BF)) based mono/hybrid epoxy composites at varying weight percentage of 2–6 wt% and evaluate the physical (void fraction and water absorption), mechanical (tensile strength, flexural strength, hardness) and sliding wear properties of as-fabricated composites. The 6 wt% NBF reinforced composites exhibited higher mechanical properties as compared to NF and BF composites with tensile strength of 34.04 MPa, flexural strength of 42.45 MPa, and hardness of 37.01 H_v respectively. The influence of various control factors (sliding velocity, NF/BF/NBF contents, normal load and sliding distance) on specific sliding wear rate of composites was evaluated by Taguchi (three factors at three levels) experimental design and the percentage contribution of these selected parameters on sliding wear performance was examined by Analysis of variance (ANOVA). The sliding wear property of as-developed composites was found to be greatly influenced by sliding velocity and the wear resistance was observed to be improved with the NF/BF/NBF contents. The wear mechanism of the as-fabricated composites has been elucidated by scanning electron microscopy analysis. The research outcomes demonstrated that the hybridization of Bauhinia vahlii fiber with Nettle fiber led to improve the mechanical and wear properties of epoxy composites.     

Liquid phase in-situ synthesis of LiF coated boron powder composite and performance study

Among practical metal additives, boron (B) has a high volumetric heating value, making it a promising choice as a fuel additive. Although B can theoretically yield a large amount of energy upon complete combustion, its combustion is retarded by the initial presence of B oxide, which coats the surfaces of B particle. To improve the ignition and combustion properties of B powder, LiOH and NH₄F were used as precursors to synthesize uniformly LiF-coated B composites (LiF-B) in situ. The LiF-B mixture was also prepared for comparison using a physical method. X-ray diffraction (XRD), Fourier-transform infrared (FTIR), scanning electron microscope (SEM), and energy-dispersive X-ray spectroscopy (EDS) were used to characterize the morphologies and compositions of the products. The thermal and combustion properties of the samples were characterized by thermal gravity-differential thermal gravity (TG-DTG), differential scanning calorimetry (DSC) and closed bomb experiment. The XRD, FTIR, SEM and EDS results demonstrated the successful preparation of the coated LiF-B sample. The TG-DTG and closed bomb experiment results indicated that the addition of LiF decreased the ignition temperature of B powder, and increasing its reaction efficiency. DSC results show that when LiF-B was added, the released heat of underwater explosive increased by 6727.2, 7280.4 and 3109.6 J/g at heating rates of 5, 10, and 15 °C/min, respectively. Moreover, LiF-B decreased the activation energy of secondary combustion reaction of explosive system as calculated through Kissinger's method by 28.9%, which indicated an excellent catalytic effect for the thermal decomposition of underwater explosive. The results reveal that LiF can improve the combustion efficiency of B powder, thereby increasing the total energy of explosives. The mechanical sensitivity increased slightly after adding LiF-B to the underwater explosive. Compared to the underwater explosive with added B, the mechanical sensitivity of the explosive with added LiF-B was significantly lower.