硅树脂添加量对氧化铝基陶瓷型芯性能的影响

以氧化铝粉末为基体,添加具有粘结性和一定陶瓷产率的硅树脂粉末,通过干压成型和无压烧结制备出氧化铝基陶瓷型芯,重点研究了硅树脂添加量对氧化铝基陶瓷型芯性能的影响。结果表明:硅树脂在裂解过程中会形成二氧化硅,二氧化硅与氧化铝基体发生反应形成新相莫来石。由于硅树脂在交联和裂解过程中会释放大量气体,导致烧结体失重,且气体的逸出会抑制由烧结引起的收缩,因此,随着硅树脂添加量增加,产生的气体量增加,烧结体的失重率增加,收缩率降低。硅树脂含量的增加使得烧结体的气孔率变大和体积密度减小,烧结体的室温抗弯强度逐渐减小。硅树脂的添加虽然降低了其室温强度,但是保证了陶瓷型芯的尺寸精度。     

预分散酚醛树脂硫化CIIR性能的研究

分别研究了预分散酚醛树脂HY-2045(预)、HY-2055(预)和SP-1055(预)对CIIR胶料硫化特性、力学性能及100℃×72h热空气老化性能的影响,并与原树脂HY-2045(原)、HY-2055(原)和SP-1055(原)的影响效果进行了对比。结果表明,与原酚醛树脂相比,预分散酚醛树脂在CIIR橡胶中的分散性、硫化胶拉伸强度和拉断伸长率均获得提高。加入SP-1055(预)可明显缩短CIIR胶料的t90;加入HY-2045(预)可使胶料的t10和t90延长,交联密度、硬度、100%定伸应力和拉伸强度均最小,拉断伸长率最大;加入HY-2055(预)可使胶料的t90延长,其他性能与加入SP-1055(预)的胶料相差不大。加入HY-2055(预)的硫化胶100℃×72h热空气老化后性能变化最小。     

高寒列车转向架防冰涂料的研究

在高寒地区运行的列车转向架部位容易发生结冰现象，这在一定程度上对行车安全造成隐患。对于平滑表面而言，表面的接触角滞后与冰粘附强度呈现线性关系，即接触角滞后越小，冰粘附强度越低。基于这一基础理论，本文意在构建低滞后的光滑涂层，实现涂层的低冰粘附强度，从而达到易除冰的效果。研究选用 HDI三聚体型多异氰酸酯为固化剂，对比了 3种商品化具有低表面能特性的含氟羟基树脂应用于双组分防冰涂料的性能差异，并采用疏水性最强、防冰性能最优的氟硅树脂制备了综合性能优异的高寒列车转向架防冰涂料。     

水性防腐涂料贮存稳定性的研究

由于水性树脂、颜料和填料等多方面的影响,水性防腐涂料在贮存中容易分层、沉淀,在不同体系中添加不同类型的触变剂可以有效地改善产品的贮存稳定性,使之在不同的环境温度下避免分层、沉淀等问题。     

Synthesis of 3,13-diglycidyloxypropyloctaphenyl double-decker polyhedral oligomeric silsesquioxane and the thermal reaction properties with thermosetting phenol-formaldehyde resin

3,13-Diglycidyloxypropyloctaphenyl double-decker silsesquioxane (EP-DDSQ) was synthesized by process of alkaline hydrolysis condensation of phenyltrimethoxysilane and corner capping reaction of methyldichlorosilane, followed by hydrosilylation with allyl glycidyl ether, and the resultant structure was confirmed by fourier transform infrared spectrometer (FTIR) and nuclear magnetic resonance (NMR), respectively. The thermosetting phenol-formaldehyde (PF) resin was then modified by EP-DDSQ, and the reactivity of PF resin with EP-DDSQ and thermal pyrolysis of modified cured resin were investigated by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The surface morphologies of modified resins at high temperature were characterized with field emission scanning electron microscope (FESEM), and chemical structure of modified resins was analyzed through X-ray photoelectron spectrometer (XPS). The results showed that the appropriate addition of EP-DDSQ did not affect the curing temperature of the PF resin itself, but could improve the heat resistance of the system. When the amount of EP-DDSQ added was 10%, the initial degradation temperature of PF resin was increased by 49.31°C, and when the amount of EP-DDSQ added was 16%, the char yield of which was reached up to 61.39%, compared with that of pure PF resin (TGA_1,000°C of 57.62%) at Ar atmosphere. More importantly, the modified resin formed a regular and dense layer of SiC and SiO_x ceramic on the surface after ablation in the muffle furnace at 800°C air atmosphere, which is very important for ablative resistant materials.     

Effect of cavosurface angle beveling on the exposure angle of enamel prisms in different cavity sizes

The quality of the micromechanical retention between the enamel prisms exposed through acid etching and adhesive system can be influenced by the relationship between the angle of the exposed enamel prisms and the external surface/restorative material. Therefore, the aim of the present study was to determine the influence of the enamel cavosurface beveling in different cavity sizes on the angle relation between enamel prisms and the restorative material. For this research, 30 human permanent molars were used and divided into three groups according the isthmus aperture of class I cavities (1/4, 1/3, and 1/2 of the intercuspal distance). Cavosurface angle beveling was performed in each tooth buccal or palatal/lingual side, and a resin composite restoration was placed. Each restored tooth was sectioned in buccal/palatal direction followed by analysis in scanning electron microscope. Means of the angles observed between enamel prisms and the restorative material were registered and statistically analyzed by Kruskal‐Wallis test. Results showed higher mean angle values for beveled groups when comparing with the values observed in the unbeveled margins (p < .05) regardless of the isthmus aperture, being 1/4 (beveled = 48.36°; unbeveled = 20.71°), 1/3 (beveled = 39.75°; unbeveled = 29.15°), and 1/2 (beveled = 37.02°; unbeveled = 26.34°). It was also observed that in some unbeveled cavities, there were the presence of laterally exposed enamel prisms (0°), mainly in more conservative cavities. It was concluded that the presence of higher angles values occurred in the samples with beveled margins, without presence of laterally exposed enamel prisms.     

Synthesis of a novel DOPO‐based polyphosphoramide with high char yield and its application in flame‐retardant epoxy resins

A novel and highly effective flame retardant (FR), DOPO‐TPMP oligomer, was synthesized by a simple condensation of 4‐(hydroxymethyl)‐2,6,7‐trioxa‐1‐phosphabicyclo[2.2.2]octane‐1‐oxide and phosphorus oxychloride followed by a polycondensation reaction with 6‐(2,5‐dihydroxyphenyl)‐6H‐dibenzo[c,e][1,2]oxaphosphinine‐6‐oxide. The chemical structure of DOPO‐TPMP was well characterized using Fourier transform infrared and NMR spectra. DOPO‐TPMP was used as an additive‐type FR for epoxy resin (EP). The FR properties of the resultant EP composites were investigated by limiting oxygen index (LOI) test, UL‐94 vertical burning test and cone calorimeter measurements. Specifically, the EP composite containing 10.0% DOPO‐TPMP achieved a LOI value of 36.1%, V‐0 rating in the UL‐94 test and a 58% reduction in peak heat release rate. Further mechanism analysis attributed the enhanced flame retardancy to the increased char yield on the addition of DOPO‐TPMP. © 2019 Society of Chemical Industry     

Chemical Recycling of Carbon Fiber Reinforced Epoxy Composites Using Mild Conditions

The increased use of carbon fiber reinforced thermosets generates more waste and end-of-life products. However, an efficient recycling method for the expensive carbon fibers has not yet been developed. The selective decomposition of amine-cured epoxy resin under mild conditions is presented. A two-step method was investigated to decompose the epoxy resin. The optimum parameters were initially determined using a model compound. By analysis of the reaction products, a cleavage of the C–N bond according to the Cope elimination could be proven. Therefore, the Cope elimination is suggested as the main step of the decomposition of amine-cured epoxy resins in presence of hydrogen peroxide. By dissolving the resin, it is possible to recover resin-free fibers with unimpaired mechanical properties.