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。     

Improved compatibility of PET/HDPE blend by using GMA grafted thermoplastic elastomer

ABSTRACT

Herein, graft-modified ethylene-1-octene copolymer (POE-g-GMA) and styrene-butadiene-styrene triblock copolymer (SBS-g-GMA) were found to be excellent reactive compatibilizers for immiscible poly(ethylene terephthalate) (PET)/high-density polyethylene (HDPE) blends via in-situ reaction compatibilization. With increase in compatibilizer amount, uniform phase morphology was observed in all the blends. Thus, exhibiting enhanced mechanical properties, especially, the notched Izod impact strength. In comparison with SBS-g-GMA, compatibilizer POE-g-GMA demonstrated greater impact on the compatibility. The addition of 15% POE-g-GMA produced blends with best mechanical properties. Besides, both POE-g-GMA and SBS-g-GMA enhanced the melt viscosity of PET/HDPE blends.     

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。     

SiO2颗粒增强酚醛树脂基摩擦材料力学性能研究

为探讨陶瓷颗粒对树脂基摩擦材料力学性能的影响,以SiO_2颗粒增强酚醛树脂基摩擦材料为例,利用三点弯曲实验研究颗粒特征对弯曲强度的影响,建立材料内部弹性应力场分布模型,并从细观力学角度进行分析。实验结果表明:添加二氧化硅陶瓷颗粒后,复合材料的弯曲强度降低、弹性模量升高;复合材料弯曲断裂截面显示脆性断裂特征,断裂过程中裂纹遇到颗粒贯穿通过;复合材料弯曲强度随颗粒含量增加而降低,随颗粒弹性模量增加先减小后增大。理论分析表明:陶瓷复合树脂基摩擦材料内部最大应力值位于颗粒边缘处;最大应力值随颗粒与基体弹性模量比值增大而增大;复合材料的平均应力与颗粒的含量成正相关。实验和理论研究表明,陶瓷颗粒添加引起材料内部应力集中,且与颗粒弹性模量和颗粒含量成正相关。     

废树脂微波处理工艺研究

废树脂微波处理工艺主要利用微波的穿透能力强和体加热的特点,首先将废树脂中的水分除去,然后将废树脂中的有机组分去除,从而达到有机废物无机化的目的。与原始废树脂相比,微波干燥、灰化处理后,得到的灰分减容和减重比均极大。利用该技术处理得到的产物,可以方便的进行后续处理。通过研究,确定了废树脂微波桶内干燥及废树脂微波灰化工艺参数。