铜包石墨对酚醛树脂基复合材料摩擦学性能的影响

目的 提高石墨与酚醛树脂的界面结合强度，改善酚醛树脂基复合材料的摩擦学性能。方法 用高温浸渗法制备铜包石墨，并制备铜包石墨-酚醛树脂基复合材料。通过摩擦磨损实验，研究铜包石墨对酚醛树脂基复合材料摩擦学性能的影响，并对比相同成分铜/石墨混合填充酚醛树脂基复合材料的摩擦学性能。通过扫描电子显微镜、能谱仪和光学显微镜对摩擦磨损表面进行分析，研究材料摩擦磨损机理。结果 石墨表面经过金属铜处理后，金属铜由分散的聚集态转变为附着态，制备的铜包石墨颗粒整体分散度高、形状好。铜包石墨-酚醛树脂基复合材料中石墨与基体界面结合紧密，保持了酚醛树脂的连续相结构，摩擦磨损表面相对平整，复合材料平均比磨损率为3.98×10^?6 mm³/(N.m)，瞬时摩擦系数波动幅度小，摩擦磨损机理以粘着磨损为主。相同成分制备的铜/石墨混合填充酚醛树脂基复合材料的界面结合度较差，摩擦磨损表面有较多裂痕，复合材料平均比磨损率为7.80×10^?6 mm³/(N.m)，瞬时摩擦系数波动幅度大，摩擦磨损机理以磨粒磨损和粘着磨损为主。结论 石墨通过表面金属铜处理，不仅能提高与基体界面结合强度，还能同时有效提高酚醛树脂基复合材料的耐磨性能和摩擦稳定性。     

Effect of pine resin derivatives on the structural,thermal, and mechanical properties of Mater-Bi type bioplastic

The effect of three additives derived from pine resin, namely, gum rosin (GR) and two pentaerythritol ester of GR, Lurefor (LF) and Unik Tack (UT), in 5, 10, and 15 wt %, on the properties of Mater-Bi, based on plasticized starch, poly(butylene adipate-co-terephthalate), and poly(ε-caprolactone) (PCL), obtained by injection molding processes, was studied. The mechanical, microstructural, and thermal properties were evaluated. LF had a cohesive behavior with the components of Mater-Bi, increasing the toughness of the material up to 250% accompanied by an increase of tensile modulus and tensile strength. UT had an intermediate behavior, conferring cohesive and plasticizing effects, allowing an increase of 105% in impact resistance. GR had a more marked plasticizing effect. This allows processing temperatures of about 50 °C lower than those used for neat Mater-Bi. In addition, an increase of the elongation at break, toughness, and impact resistance in 370, 480, and 250%, respectively, was achieved. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 48236.     

基于聚集诱导发光效应的高固低黏丙烯酸荧光树脂的制备及其性能研究

为了研制一种具有荧光功能特性的高固低黏羟基丙烯酸树脂。从聚集诱导发光效应（AIE）出发，将具有 AIE性质的二对丙烯酸四苯乙烯酯荧光分子通过自由基共聚连接于聚合物链段。由于聚合物链段对荧光分子化学键固定以及聚合物链的包裹束缚作用，导致荧光分子运动受限，从而实现涂层在紫外灯下荧光发光。通过荧光光谱的实时跟踪，探索高固低黏羟基丙烯酸树脂的合成以及固化规律。此外，由于聚合物链段对外界刺激具有实时响应性，从而间接影响了所连接的荧光分子的荧光发光行为。因此，文中也探索了涂层在外界温度与化学气体的影响下所发生的荧光变化的规律，以探索其在功能涂层中应用的可行性。     

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 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.     

户内热转印粉末涂料用混合型聚酯树脂的合成研究

通过分析热转印性能的影响因素合成了不同结构的聚酯树脂，研究了树脂酸值对热转印性能的影响，同时研究了部分单体对聚酯树脂热转印性能的影响。采用 DSC热分析法研究了固化促进剂对粉末涂料固化行为的影响，结果表明：选择合适的固化促进剂对涂层转印性能的提高有至关重要的作用。     

轨腰仿生自分层防腐梯度涂料合成及影响因素和结构探究

目的仿荷藕结构及功能,制备一种自分层防腐涂料。方法合成聚氨酯改性环氧树脂(PU/EP)及氟硅改性丙烯酸树脂(氟硅改性PAA),将两种树脂共混形成自分层涂料。通过铅笔硬度测试、机械性能测试、接触角测试、耐老化测试、划格法附着力测试、电化学阻抗测试等,分别评价两种树脂比例、混合溶剂比例对涂膜自分层行为及性能的影响,并通过SEM-EDS、红外光谱等表征技术分析涂膜分层后的结构。结果当PU/EP∶氟硅改性PAA=1∶1时,接触角达到96.0°,柔韧性为0.5 mm,耐冲击为50 cm,附着力等级为1,失光率降至19%;乙酸丁酯(NBAC)∶正丁醇(NBA)=4∶6时,涂膜分层情况良好,接触角达到107.7°,浸泡水中48 h耐水性无变化,失光率降至17%。SEM-EDS、红外光谱分析表明,自分层涂膜上层为氟硅改性PAA、底层为PU/EP,中间存在过渡涂层,过渡层两种树脂中的─COOH、─OH、环氧基发生反应,使整个涂层更具稳定性。经由EIS分析,在3.5%NaCl溶液中浸泡40天后,腐蚀介质没有渗透涂膜到达基底金属界面。结论制备的轨腰仿生自分层涂膜的机械性能、附着力、疏水性、耐老化、防腐蚀性能优异,涂膜结构稳定。     

碳纤维/乙烯基酯树脂复合材料拉伸性能研究

研究了碳纤维进行氧化处理、铺层形式,以及紫外光照射和不同溶液介质浸泡处理等,对碳纤维/乙烯基酯树脂复合材料拉伸性能的影响。结果表明:碳纤维最佳氧化工艺为浓硝酸氧化1 h,空气氧化温度250℃,空气氧化30 min。碳纤维最佳铺层设计为[0°,0°,45°]2s。随紫外光照射时间增加,复合材料拉伸强度呈先增后降趋势,120 h时达最大值。溶液介质浸泡会降低复合材料的拉伸强度。温度相同溶液介质不同时,复合材料在NaOH溶液中拉伸强度降低程度最大,温度提高会加速复合材料失效老化。     

Wet Oxidation Treatment of Radioactive Spent Ion-Exchange Resin

Radioactive waste ion-exchange resins have been treated by cement solidification directly, however, the effect of cement is unsatisfactory. In order to find other proper treatment methods, many investigations have been carried out. Especially, wet oxidation treatment technology is favored by many researchers because of its short treatment cycle and high volume reduction ratio. In this work, the reaction mechanism, process characteristics and industrial application of the wet oxidation treatment of radioactive spent ion-exchange resins were summarized. The analysis of the acid boiling degradation, Fenton wet oxidation technology, steam reforming process and supercritical water oxidation method had been focused. Mainly for the acid digestion, steam reforming process, supercritical water oxidation and Fenton wet oxidation were compared by the status of research at home and abroad and industrial applications, combined with the advantages and disadvantages of each method and the ease of post-processing,and considering the perspective of nuclear safety and convenient for subsequent processing, four treatment methods were briefly analyzed by comparing the advantages and disadvantages of each method. The results indicated that Fenton wet oxidation treatment of radioactive spent ion exchange resin was one of the feasible schemes.     

环氧树脂涂层表面亲水性对微藻黏附性能的影响

在固体材料表面黏附成膜是微藻细胞的一种生理特性。近些年基于微藻生物膜的生物过程，如生物膜贴壁培养和防附着技术受到了很多关注。微藻在固体材料表面的黏附受藻细胞与材料表面之间的相互作用的影响，建立黏附强度与材料表面性质参数间的关系对于通过材料选择来强化或控制微藻生物膜具有非常重要的意义。本工作的目的是揭示和明确材料亲疏水性对微藻黏附的影响，提出了一种双酚A环氧(EP)树脂表面亲疏水改性的方法。通过将亲水性的二乙醇胺(DEA)或疏水性的聚甲基聚硅氧烷(PMHS)加入到EP树脂中反应，EP树脂表面水接触角在36.80?~98.34?范围内可通过加入不同量的DEA或PMHS实现任意可调，材料的表面水接触角与DEA或PMHS加入量之间有线性关系。重要的是这种改性方法获得的材料，其形貌、结构、表面粗糙度等表面性质几乎没有变化，从而在研究和关联微藻黏附量与材料表面亲疏水性(表面水接触角)之间的关系时可以排除亲疏水性之外的其他表面性质的影响；其次，考察了小球藻和栅藻在不同亲疏水性材料表面的黏附行为，结果表明小球藻和栅藻在亲水性和疏水性材料表面均能黏附成膜，但在亲水性材料表面黏附更多更快；建立了微藻最大黏附容量与材料表面接触角之间关联关系，表明微藻最大黏附容量随材料表面水接触角的增大而线性降低，栅藻的表面黏附容量比小球藻大。