分离有机/有机混合物的PVA、CA系列膜及其渗透汽化性能研究(Ⅱ) 成膜条件对渗透汽化性能的影响

用溶剂完全蒸发法制备了PVA复合膜 .经对MTBE/MeOH混合物的分离实验得到了PVA复合膜的最佳成膜条件 ,即 :铸膜液中PVA、马来酸浓度分别为 7%、3% ,热处理温度130～ 15 0℃ .在 1%～ 2 %丙酮水溶液中浸泡处理 4～ 8h ,CTA中空纤维RO膜被改性成渗透汽化膜 .CTA中空纤维膜的分离性能优于其它醋酸纤维素系列膜 ,PVA/CA复合膜的性能优于PVA/PAN复合膜和CA/PAN复合膜     

Photoinitiated cationic polymerization using a novel phenacyl anilinium salt

A novel phenacyl anilinium salt, N-phenacyl, N,N-dimethylanilinium hexafluoroantimonate, (PDA), has been synthesized and used as photoinitiator for cationic polymerization of cyclohexene oxide (CHO), butyl vinyl ether (BVE) and N-vinyl carbazol (NVC). Plausible mechanism of the photoinitiation involves the decay of the excited PDA with both heterolytic and homolytic cleavages of carbon-nitrogen bond. Thus, phenacylium cations formed directly or subsequent intermolecular electron transfer, respectively, initiate the polymerization.     

VNS反应合成LLM-116

以1,3-二硝基吡唑为原料,经热重排、氨气中和得到3,5-二硝基吡唑铵盐,然后酸化得到3,5-二硝基吡唑。以三甲基肼碘化物（TMHI）作为异常亲核取代氢（VNS）反应试剂,与3,5-二硝基吡唑在叔丁醇钾为催化剂,利用VNS反应合成4-氨基-3,5-二硝基吡唑（LLM-116）。采用红外分析、核磁共振、元素分析等仪器鉴定了其结构,讨论了VNS反应机理及影响因素。通过实验,得出最佳VNS反应试剂为TMHI,反应时间为4h,反应温度为25℃,收率达到60%。     

有机纤维材料用软膜乳液阻燃剂的制备

采用甲醛、尿素、三聚氰胺、脒基脲磷酸盐为原料,以硼砂、硼酸、氨水为pH调节剂合成了保护胶;在保护胶存在下,以预乳化的丙烯酸酯混合单体于82-88℃共聚合成乳液,将其涂布于有机纤维材料,干燥后得软膜透明阻燃涂层。用其处理的涤棉布阻燃性能为:损毁长度68mm、续燃时间1s、阴燃时间3s、氧指数62、吸附干量287g/kg,处理的纸板的阻燃性能为:平均炭化长度77mm、平均续焰时间2s、平均续灼燃时间32s、吸附干量283g/kg。     

铂与氢、水和苯分子相互作用的量子化学研究

采用量子化学程序Gaussian98(A.9)从头算的B3LYP方法，全优化计算铂对氢、水和苯的化学吸附作用，得到了3种相关络合物PtX、PtXX和Ptxxx(X=H，H2O或C6H6)的平衡几何构型和电子结构信息，并探讨了这些络合物的成键性质，以及苯环与铂原子之间的分子轨道作用性质。结果表明，苯环与铂原子之间有很强的成键作用，并随着游离氢原子和水分子的参与，作用强度有很大变化。苯分子吸附在金属铂上，它的芳香性得到不同程度的降低，苯环被活化，苯环与铂原子之间形成η^2型π键络合物；水参与作用后，苯环与铂原子之间形成σ络合物；氢和水同时参与作用后，苯环与铂原子之间仅有很弱的π轨道作用。     

EO/EG装置生产过程中有机酸的生成原因分析

分析了环氧乙烷，乙二醇装置工艺系统中有机酸生成的原因．指出在银催化剂作用下，乙烯氧化过程有机酸生成主要成分是甲酸和乙酸，银催化剂不是影响氧化反应器出口醛含量的主要因素；杂质、温度等对反应器出口气中的醛含量有重要影响，也直接影响到装置前系统的有机酸含量；乙二醇后系统中有机酸的增加仅取决于两级吸收及解析工艺的稳定操作。     

Alkylated ureas: mineralization and evaluation as N sources

An incubation experiment was conducted for 11 weeks to study the mineralization of ten alkylated ureas and urea in soil. Six of the alkylated ureas viz. methylurea(MU), 1,3-dimethylurea(1,3DMU), 1,1-dimethylurea(1,1DMU), ethylurea(EU), 1,3-diethylurea(1,3DEU) and butylurea(BU) and urea mineralized during the experiment. Urea mineralized immediately, while alkylated ureas mineralized after an incubation period ranging from less than a week to four weeks (delay period of mineralization). The delay period increased in the following sequence MU < 1,3DMU < EU < BU < 1,1DMU < 1,3DEU, but after the delay period was over the compounds mineralized almost as rapidly as urea. The delay period varied according to the number of carbon atoms in the alkyl group and their position with respect to each other on the molecule. It appeared to be specific for each compound and was apparently not influenced by the presence of urea or other alkylated ureas. This character can be used to develop mixture of various alkylated ureas to obtain N mineralization at the desired time. Rapid evolution of CO₂ and N₂O was observed during the mineralization of urea as well as alkylated ureas. Increase in soil pH was also observed during this period. The simultaneous ocurrence of these events suggested the formation of urea as an intermediate during the mieralization of alkylated ureas. None of the alkylated ureas showed adverse affect on emergence of wheat seedlings and except DEU and BU at high concentration no other alkylated urea showed any adverse effect on initial growth of wheat seedlings.     

一种新型有机非线性光学材料的光折效应及其产生机理

本文介绍了一种新近研制的光折聚合物。实验表明，除去吸收和反射，入射光束经聚合物后的第一布拉格衍射效率高达８６％，材料也显示出双光束耦合的净增益高于２４０ｃｍ＾－１。这些结果表明，这种新型研制的光折聚合物材料是替代无机光折晶体的实用材料。     

复杂场景实时目标检测方法

针对含有非平稳背景的复杂场景,提出一种基于空间混合高斯模型的实时目标检测方法.该方法以混合高斯模型作为颜色分布的统计框架,并在空间邻域中利用背景与前景隶属度之间的竞争确定像素的归属,提高了检测准确率;同时通过基于偏差均值的匹配判断和低权重模型的移除提升了混合高斯统计框架的性能,以实时地对运动目标进行准确的检测.实验结果表明,文中方法对非平稳背景有很好的适应能力,在检测准确率和运行效率上均优于其他检测方法.