有机硅乳液稳定性的研究

以阳离子型乳液聚合为例，详细讨论了聚合反应因素及环境因素对环氧改性有机硅乳液稳定性的影响。结果表明：在聚合反应温度为65℃、催化剂的用量为总加料量的0．3％～0．5％、硅烷偶联剂的用量为D4质量的3％～5％、乳化剂用量为总加料量的10％、阳／非离子型乳化剂的质量比为1．5～1．8、D4与水的质量比为0．3～0．4条件下，制得的环氧改性有机硅乳液稳定性良好；采取急冷的方式中止聚合反应，并以醋酸中和至pH值为6～7，有利于环氧改性有机硅乳液稳定性的提高。     

气相色谱仪在丙基型硅烷偶联剂催化合成中的应用

通过筛选获得了最佳色谱条件，建立较为可行的丙基型硅烷偶联剂催化合成气相色谱分析方法，为实验室研究合成硅烷偶联剂探索高效催化剂提供了快速的检测方法。     

玫瑰红RB催化纤维的制备及其在交叉脱氢偶联反应中的应用

以聚丙烯腈纤维为载体,通过乙二胺接枝改性,有机光催化剂-玫瑰红RB吸附,制备了一种腈纶负载光催化纤维。在其催化N-苯基四氢异喹啉及其衍生物和硝基甲烷的交叉脱氢偶联反应中,反应温度85℃,乙二胺用量60 mL,水用量100 mL,反应时间240 min,氨基接枝量1.61 mol%时,对RB染料的吸附量可达9.2%,收率均在81%以上,并在8次循环反应后仍然保持良好的稳定性和催化活性。     

大凌河流域初始水权分配实践评价

结合大凌河流域初始水权分配实践,从分配范围、分配机制、分配原则、分配模型等方面,对现有研究成果进行全面梳理。在此基础上,结合大凌河流域特点,借鉴我国流域水资源配置评价指标体系,从公平性、效率性、可持续发展、政府宏观调控4个维度,设计了一套水权分配评价指标体系,进而构建了初始水权分配实践效果的耦合评价模型,并应用于大凌河流域。结果表明,在政府和大凌河流域水行政管理部门的宏观调控作用下,通过加强大凌河流域所在区域的政治民主协商,流域内各区域水权分配结果充分体现了与其社会经济发展之间的匹配性,且各区域之间的耦合协同发展效度均达到较高水平。     

State estimation for complex systems with randomly occurring nonlinearities and randomly missing measurements

This paper is concerned with the state estimation problem for the complex networked systems with randomly occurring nonlinearities and randomly missing measurements. The nonlinearities are included to describe the phenomena of nonlinear disturbances which exist in the network and may occur in a probabilistic way. Considering the fact that probabilistic data missing may occur in the process of information transmission, we introduce the randomly data missing into the sensor measurements. The aim of this paper is to design a state estimator to estimate the true states of the considered complex network through the available output measurements. By using a Lyapunov functional and some stochastic analysis techniques, sufficient criteria are obtained in the form of linear matrix inequalities under which the estimation error dynamics is globally asymptotically stable in the mean square. Furthermore, the state estimator gain is also obtained. Finally, a numerical example is employed to illustrate the effectiveness of the proposed state estimation conditions.     

HT-730改性酚醛-丁腈胶粘剂的研制

对酚醛-丁腈胶粘剂进行改性，添加5．0％的硅烷偶联剂，改善了酚醛-丁腈胶粘剂的工艺性能，提高了粘接强度，特别是降低了酚醛-丁腈胶对环境湿度的敏感性。研制的HT-730胶在环境湿度90％时仍有很高的粘接强度，同时老化性能和适用期并没有受到影响。     

废渣粉煤灰纤维棉增强PVC复合材料

本文选用废渣制成的粉煤灰纤维棉(FAF)和聚氯乙烯(PVC)树脂作为原料,成功制备了FAF/PVC复合材料,研究了FAF的表面处理及其加入量对复合材料力学性能、热性能和硬度的影响,并用SEM对复合材料的界面进行了表征。实验结果表明,相对于纯PVC树脂而言,复合材料含经KH550处理的FAF40phr时,拉伸强度提高约12%;含经软化剂处理的FAF10phr时,冲击强度提高约110%;含经偶联剂和软化剂联合处理的FAF10phr时,冲击强度提高约70%,拉伸强度提高约11%,维卡软化温度随FAF添加量的增加呈上升趋势。研究结果证明,KH550和软化剂联合使用会对复合材料起到有效的增强增韧效果,因此能提高复合材料中FAF的填充量。制成的环保型FAF/PVC复合材料不仅性能全面高于纯PVC,而且材料成本显著降低,为综合利用废渣FAF开拓了新方向。     

AN EXPERIMENTAL STUDY OF METHANE OXIDATIVE COUPLING IN FIXED BED REACTORS WITH A DISTRIBUTED OXYGEN FEED

Methane oxidative coupling has been carried out in a reactor with a distributed oxygen feed. The system consists of a catalytic bed of Li/MgO in a quartz reactor with one inlet for methane and one or more inlets for oxygen. To enable the comparison between the co-fed mode and the distributed feed mode, an especial experimental design was used in order to maintain the same contact time in the co-fed and in the distributed feed modes, and in order to minimize the temperature gradients caused by the exothermic oxidation process. The results clearly show that a distributed oxygen feed may give rise to significant increases in the hydrocarbon selectivity obtained at a given methane conversion,     

PMDA-6FHP-DR1／SiO2杂化纳米材料的结构设计和合成

以含氟的二胺5，5′—(六氟异丙基)—二—(2—氨基苯酚)及均苯四甲酸酐(PMDA)为单体，首先合成了经酰胺化的主链上带有活性羟基的含氟聚酰亚胺，再通过Mitsunobu反应将活性生色分子分散红1(DR1)共价链接到聚酰亚胺的侧链骨架上，合成了含氟聚酰亚胺．采用溶胶—凝胶(SOl—Gel)技术，并利用偶联剂γ—氨丙基三乙氧基硅烷(AFTES)制备带有发色团的和含有硅氧烷端分子的聚酰胺酸，其中的Si(OR)3基经水解、缩合后，与正硅酸乙酯(TEOS)在催化剂作用下反应，经杂化、凝胶后，得到光学透明且热稳定性高的有机／无机杂化材料．将制得的含氟聚酰亚胺／SiO2杂化材料，采用红外光谱(FT—IR)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、X射线衍射(XRD)、示差扫描量热法(DSC)，对材料的结构、表面形貌、热性能进行了表征．     

Relationship Between Interfacial Water Layer Adhesion Loss of Silicon/Glass Fiber-Epoxy Systems: A Quantitative Study

Water at the polymer/substrate interface is often the major cause of adhesion loss in coatings, adhesives, and fiber-reinforced polymer composites. This study critically assesses the relationship between the interfacial water layer and the adhesion loss in epoxy/siliceous substrate systems. Both untreated and silane-treated Si substrates and untreated and silane-treated E-glass fibers were used. Thickness of the interfacial water layer was measured on epoxy/Si systems by Fourier transform infrared-multiple total internal reflection (FTIR-MTIR) spectroscopy. Adhesion loss of epoxy/Si systems and epoxy/E-glass fiber composites was measured by peel adhesion and short-beam shear tests, respectively. Little water accumulation at the epoxy/Si substrate interface was observed for silane-treated Si substrates, but about 10 monolayers of water accumulated at the interface between the epoxy and the untreated Si substrate following 100 h of exposure at 24 °C. More than 70% of the initial epoxy/untreated Si system peel strength was lost within 75 h of exposure, compared with 20% loss after 600 h for the silane-treated Si samples. Shear strength loss in composites made with untreated E-glass fiber was nearly twice that of composites fabricated with silane-treated fiber after 6 months of immersion in 60 °C water. Further, the silane-treated composites remained transparent, but the untreated fiber composites became opaque after water exposure. Evidence from FTIR-MTIR spectroscopy, adhesion loss, and visual observation strongly indicated that a water layer at the polymer/substrate interface is mostly responsible for the adhesion loss of epoxy/untreated siliceous substrate systems and epoxy/untreated glass fiber composites and that FTIR-MTIR is a viable technique to reliably and conveniently assess the adhesion loss attributable to water sorption at the interface.