无明胶重铬酸盐全息记录软片的正性光抗蚀特性

对无明胶重铬酸盐全息记录软片（ＮＧＤ）的光正性抗蚀特性进行了分析研究，通过对溶解度的分析及红外光谱的测定，首次提出ＮＧＤ是一种新型的紫外正性光抗蚀材科，给出了实验及分析结果。     

玻璃两面重叠手印拍摄机理

根据斯涅尔定律和菲涅尔公式阐述清水衬底法消除玻璃下界面手印或玻纹的影像，以及用偏振光，紫外线拍摄玻面痕迹的方法和机理。     

阻燃玻璃纤维增强PA6的紫外光稳定性

分别将三聚氰胺氰尿酸盐、十溴二苯乙烷、溴化聚苯乙烯和次磷酸盐作为阻燃剂对尼龙6(PA6)进行阻燃玻璃纤维增强改性,采用热失重分析仪、水平垂直燃烧测定仪、分光测色仪对PA6复合材料的热降解行为、阻燃性能和紫外光老化后色差值(ΔE)进行了分析。结果表明,阻燃剂的引入提升了PA6复合材料的阻燃性能,但是降低了复合材料的热稳定性。阻燃剂类型对PA6复合材料紫外光黄变的影响程度依次是溴化聚苯乙烯>十溴二苯乙烷>三聚氰胺氰尿酸盐、次磷酸盐。通过将紫外光吸收剂和中性受阻胺光稳定剂复配使用可以有效抑制溴化聚苯乙烯阻燃增强PA6材料的紫外光黄变。     

充油SEBS的结构、力学性能和紫外辐照稳定性

自制了一种中间基的苯乙烯-乙烯/丁烯-苯乙烯三嵌段共聚物(SEBS)弹性体用填充油,并从分子结构及微相结构上分析了线型和星型SEBS充油体系的力学性能、紫外辐照稳定性与其结构的关系。通过小角X射线散射(SAXS)、透射电子显微镜(TEM)表征了SEBS充油体系的微观结构,揭示了SEBS分子结构是影响充油体系微观结构的主要因素,且软硬段电子密度差以及PS相间距越大,SEBS的微相分离程度越高。结合Instron万能材料试验机的测试结果,发现SEBS微相分离程度高有利于充油体系力学性能的提高。通过傅里叶红外光谱(FTIR)研究了经紫外辐照后SEBS体系的化学结构变化,结果显示,经紫外辐照后的体系均在1700~1740 cm-1、1800 cm-1附近出现吸收峰,且吸收峰强度越大,力学性能下降得越快,表明氧化降解是造成SEBS体系力学性能下降的主要因素。     

Degradation of 2,4-D By Ozone And Light

The decomposition of 2,4-dichlorophenoxyacetic acid in aqueous solutions has bsen studied using ozone and ultraviolet radiation at different pH, ozone production, and initial concentration of pesticide. A mathematical model which incorporates the rate of mass transfer of ozone, the oxidation kinetics of 2,4-D and the kinetics of formation and oxidation of the intermediates was used. A global rate constant was calculated and an empirical equation which correlated that constant with ozone production, initial concentration of 2,4-D and pH at the same temperature was determined.     

用紫外吸收光谱法测定粗蒽中菲、蒽的含量

用紫外吸收光谱法同时测定粗蒽中菲、蒽的含量,结果表明,采用环已烷作溶剂,吸收波长分别为293nm和357nm,在0.004～0.04g/L范围内,菲、蒽符合线性关系。该方法操作简单、测定迅速、结果准确。     

The Chemistry of Water Treatment Processes Involving Ozone,Hydrogen Peroxide and Ultraviolet Radiation

Advanced oxidation processes are defined as those which involve the generation of hydroxyl radicals in sufficient quantity to affect water purification. The theoretical and (practical yield of OH from O₃ at high pH, 0₃/H₂0₂, O₃/UV and H₂O₂/UV systems is reviewed. New data is presented which illustrates the importance of direct photolysis in the O₃/UV process, the effect of the H₂0₂:0₃ ratio in the O₃/H₂O₂ process, and the impact of the low extinction coefficient of H₂O₂ in the H₂0₂/UV process.     

Adhesion properties of UV crosslinked polystyrene-block-polybutadiene-block-polystyrene copolymer and tackifier mixture

The peel and tack properties of mixtures of polystyrene-block-polybutadiene-block-polystyrene (SBS) and a tackifier were investigated after these were crosslinked by ultraviolet (UV) irradiation at various amounts of benzophenone (BP) as a photoinitiator and trimethylolpropane mercaptopropionate (TRIS) as a crosslinking agent.The degree of crosslinking of polybutadiene (PB) block in the SBS mixture was qualitatively estimated from the amount of gel fraction as well as the change in the glass transition temperature of the PB block. The crosslinking of the PB block was done within 3 min after UV irradiation and the peel strength of crosslinked specimens was as low as 45[percnt] of specimens without crosslinking. Nano-tack and bulk tack properties as well as the surface tension of mixtures were measured depending upon amounts of BP and TRIS.     

The effects of temperature, relative humidity and reducing gases on the ultraviolet response of ZnO based film bulk acoustic-wave resonator

This study investigated the influence of temperature, relative humidity and reducing gases on the ultraviolet (UV) response of ZnO based film bulk acoustic-wave resonator (FBAR). As temperature increased, the UV response of the FBAR degraded. This was attributed to the softening of the ZnO film with increasing temperature. Water molecules can replace adsorbed oxygen on the ZnO surface. At high relative humidity, more oxygen was replaced by water. In this way, the density of the ZnO film increased and less oxygen was left on the surface to be desorbed by UV, both of which contributed to a lower UV response. Reducing gases, such as acetone, can react with the surface adsorbed oxygen and reduce the density of the ZnO film, resulting in UV response degradation.     

Tailoring the adhesion of optical films on polymethyl-methacrylate by plasma-induced surface stabilization

Adhesion of plasma-deposited optical and protective coatings, such as amorphous hydrogenated silicon nitride, SiN_1.3, on polymethyl-methacrylate (PMMA) substrates has been found to be limited by a cohesive failure inside the PMMA bulk. Using direct exposure to a low pressure plasma in helium or to vacuum ultraviolet (VUV) radiation generated from plasma, the adhesion of SiN_1.3 at high humidity and elevated temperature has been substantially increased. Using a multitechnique analytical approach, the enhanced adhesion was attributed to the initial etching of the weak boundary layer followed by formation of a crosslinked, graded, mechanically stabilized layer in the interfacial region (interphase), which possesses a physical thickness of 50 to 100 nm and a microhardness of about 2 GPa.