马来酸酐在炭黑表面接枝聚合的研究

研究了过氧化苯甲酰引发马来酸酐在炭黑表面的接枝聚合反应，探讨了反应时间、引发剂用量、接枝单体用量对接枝率的影响。结果表明，接枝率随反应时间的延长而增加，但２ｈ后，接枝率增加不多；随引发剂用量的增加，接枝率呈上升趋势，但用量在１５ｍｇ以后，接枝率趋于定值；随接枝单体用量的增加，接枝率直线上升。在本实验条件下，接枝率达到９％。通过接枝产物的Ｘ射线光电子能谱及红外分析可以证实，马来酸酐已接枝到炭黑表面。从光学显微图像分析结果可知，马来酸酐接枝改性对炭黑在聚合物基体中的分布和分散性能起到良好的改善作用。     

一种改进的超宽条带噪声消除算法

针对高光谱遥感图像中的超宽条带噪声干扰现象,在深入研究高光谱图像特点和条带噪声产生机理的基础上,提出了一种新的基于最小序列值、小波变换和矩匹配相结合的滤波算法（OWM算法）。该算法主要包括灰度对比度处理、最小序列值处理、小波变换系数归零处理和矩匹配处理等四个步骤。用实际的高光谱图像进行了一系列的验证比较实验,获得了好的实验效果。实验结果表明OWM算法不仅能够有效滤除高光谱图像中的超宽条带噪声,而且还具有较好的普适性。     

基于间歇测量的状态估计稳定性和精度研究*

针对分布式控制系统状态估计过程出现的测量值丢失问题,本文量化分析测量值丢失对估计稳定性和精度的影响。首先,根据随机测量模型重新推导带测量值丢失的卡尔曼滤波器,得到估计误差协方差迭代式。然后,将随机误差协方差迭代式建模为修正的黎卡提微分方程,提出了估计稳定性和精度分析方法。最后,列举不同的系统实例,证明临界包到达率的存在性,当测量值到达率大于临界值时,平均误差协方差从发散过渡到有界,进而得到估计精度与包达率之间的函数关系。     

二十八烷醇的研究进展

本文介绍了二十八烷醇的来源、理化性质、提取工艺以及二十八烷醇的生理功能,概括了二十八烷醇在医药、食品、化妆品和饲料等多个领域中的应用进展。     

聚氨酯在聚合物电解质中的应用进展

简述了聚合物电解质的特点和发展前景,介绍了聚醚型聚氨酯、聚硅氧烷改性聚氨酯、聚丙烯腈改性聚氨酯、聚丙烯酸酯改性聚氨酯作为聚合物电解质基体材料的最新研究进展。聚氨酯由于其性能优良,作为聚合物电解质基体材料具有良好的研究和开发前景,特别是聚合物电解质作为新型锂离子二次电池的电解质材料具有非常大的发展潜力。     

生物膜载体吸附剂对Zn2+的吸附

本文对生物膜吸附Zn^2＋的行为进行了准一级动力学方程和Elovich模型方程的拟合，对实验测定的吸附等温线用Langmuir与Freundlich吸附模型进行拟合；考察了pH值及温度对生物膜吸附Zn^2＋的影响。结果表明，Zn^2＋在生物膜载体吸附剂上的吸附动力学过程与Elovich方程有较好的拟合度，R^2=0．99994。单一等温吸附过程与Langmuir方程具有较好的拟合度，R^2=0．99785；pH=6～8，室温25℃对Zn^2＋分有较高的去除率。     

The compatibility of the blends of PUs with PVC and the adhesion behavior of PU to PVC

Three series of polyurethane adhesives—polyethyleneadipateurethane (PEAU), polybuthyleneadipateurethane (PBAU), and polyhexyleneadipateurethane (PHAU)—with the same MW and hard/soft segment ratio, based on the three polyesters polyethyleneadipate (PEA), polybuthyleneadipate (PBA), polyhexyleneadipate (PHA), with 4,4′-diphnylmethane diisocyanate (MDI), and butendiol were synthesized by solution polymerization. The crystallinity of these polyesters and polyurethanes (PUs) and the compatibility of blends of PUs with PVC were studied by means of wide-angle x-ray diffraction (WAXD), differential scanning calorimetry (DSC), dynamic thermomechanical analysis (DMA), testing of solubility, and phase contrast microscopy. The results indicated that PBAU/PVC and PHAU/PVC were compatible systems, but PEAU/PVC was incompatible. The adhesive strengths of the three adhesives were quite different from one another, in the order of PBAU ≥ PHAU ? PEAU. The influences of crystallinity and compatibility on adhesion were discussed, and the Diffusion Theory for PU-PVC systems was recommended. © 1995 John Wiley & Sons, Inc.     

Benzene Alkylation with Propane over Mo Modified HZSM-5

Benzene alkylation with propane has been studied over HZSM-5 loading 3.1–15.4 wt% Mo in continuous-flow microreactor under 350 °C and atmospheric pressure with the highest activity obtained at 6.7 wt% Mo loading. C_7–9 aromatics were obtained as main products while the total amount of benzene rings kept unchanged. i-Propylbenzene and n-propylbenzene are formed primarily, while toluene, ethylbenzene, and ethyl-toluene are formed secondly from the propylbenzenes. Catalytic performance of 6.7 wt% Mo/HZSM-5(38) partially poisoned by NH₃ shows that the strong acid sites play a crucial role in the alkylation. Low SiO₂/Al₂O₃ ratio of HZSM-5 in the Mo modified catalysts gives high propane conversion. Two hydrothermal treatment methods were applied to the 6.7 wt% Mo/HZSM-5(38) catalyst, caused decrease of propane conversion but result in different product distribution. A possible reaction mechanism concerning bifunctional active centers resulted from combination of loaded Mo species and strong acid centers on HZSM-5 is proposed.     

A paraffin-fueled SOFC system design and integration

This paper addresses an integrated design of paraffin-reformer, gas separations and the electricity production with a solid oxide fuel cell (SOFC). The overall design consists of three modules. First module is a system of paraffin reformer. In this module, the paraffin feed stream is to send to a steam-reformer. In the second module, the gas separations method illustrated is the combination of a methane-permeable membrane with a pressure-swing adsorption (PSA). In the third module, the purified hydrogen is fed to the SOFC unit. To be energy efficient, this paraffin-fueled SOFC system is designed with the consideration of heat integration. The intent of this paper is to provide a possible, alternative way of cogeneration systems for refinery and petrochemical plants.     

Low temperature SCR of NO with NH3 over carbon nanotubes supported vanadium oxides

A novel multiwalled carbon nanotube (CNTs) supported vanadium catalyst was prepared. The structure of catalyst prepared was characterized by TEM, BET, FTIR, XRD and temperature-programmed desorption (TPD) methods. The results indicated that vanadium particles were highly dispersed on the wall of carbon nanotubes. The V₂O₅/CNT catalysts showed good activities in the SCR of NO with a temperature range of 373–523 K. The Lewis acid sites on the surface of V₂O₅/CNT are the active sites for the selective catalytic reduction (SCR) of NO with NH₃ at low temperatures. It was suggested that the reaction path might involve the adsorbed NH₃ species reacted with NO from gaseous phase and as well as the adsorbed NO₂ species. The diameter of CNTs showed positive effect on the activities of the catalysts. Under the reaction conditions of 463 K, 0.1 Mpa, NH₃/NO = 1, GHSV = 35,000 h⁻¹, and V₂O₅ loading of 2.35 wt%, the outer diameter of CNTs of 60–100 nm, the NO conversion was 92%.