动态硫化EPDM／PP热塑性弹性体相态结构及其力学行为

研究动态硫化ＥＰＤＭ／ＰＰ热塑性弹性体相态结构及其力学行为。结果表明：动态硫化ＥＰＤＭ／ＰＰ共混物相态是ＥＰＤＭ橡胶以颗粒状分布在ＰＰ连续相中,这种相态结构一般不随橡塑比的变化而改变,但ＥＰＤＭ橡胶颗粒的形态变化显著。动态硫化ＥＰＤＭ／ＰＰ共混物,在橡塑比小于２５／７５,共混物具有类似橡胶应力－应变特征。     

聚丙烯／顺丁橡胶动态硫化法增韧

用简单共混和动态硫化共混两种不同工艺制取ＰＰ／ＢＲ共混物，分别测定了两种共混物在室温和低温下的冲击强度，用扫描电镜（ＳＥＭ），动态粘弹谱（ＤＤＶ）和偏光显微镜等手段对共混物进行了分析。结果表明，动态硫化共混法，可以减小ＰＰ球晶尺寸，增加ＰＰ球晶分布的均匀性，有效地改善共混物的形态结构，增加两相的相容性；提高共混物的冲击强度，特别是低温下的冲击强度。研究工作为用动态硫化法进一步提高顺丁橡胶（ＢＲ）增韧ＰＰ的效果提供了实验依据。     

动态硫化EPDM／PP热塑性弹性体的流变性能

研究了共混工艺条件，橡塑比，橡胶相交联速率及交联密度，ＰＰ的熔体流动指数对ＥＰＤＭ／ＰＰ共混物流变性能的影响。结果表明，当降低ＥＰＤＭ含量，减小ＥＰＤＭ相粒径时，共混物的流动性增强。共混物发生熔体破裂是由于ＥＰＤＭ和ＰＰ相在挤出后两相大分子的弛豫行为不同所致。提高ＰＰ含量，降低了ＥＰＤＭ相粒径，同时ＥＰＤＭ分散相具有适宜的交联密度时，可以得到挤出表面光滑的共混物。     

动态硫化EPDM/PP共混型热塑性弹性体的研究

研究了ＥＰＤＭ／ＰＰ共混比、不同牌号ＰＰ、硫化体系、混炼方式和软化剂用量对动态硫化ＥＰＤＭ／ＰＰ共混物性能的影响。研究结果表明,当ＥＰＤＭ／ＰＰ共混比为６５／３５,经一步混炼法制出的共混物的拉伸强度大于８ＭＰａ,扯断伸长率达４００％,撕裂强度为４０ｋＮ·ｍ－１,屈挠寿命大于１０万次,邵尔Ａ型硬度为７０～８０度。软化剂用量在３０份以内为宜。     

不同硫化体系动态硫化EPDM/PP热塑性弹性体流变性能的研究

研究了不同硫化体系、硫化剂用量及共混比对ＥＰＤＭ／ＰＰ共混物流变性能的影响。结果表明,选择酚醛树脂硫化体系、控制酚醛树脂用量为５ 份以及ＥＰＤＭ／ＰＰ共混比为５０／５０,可以得到挤出表面最为光滑的共混物。     

动态硫化EPDM/PP共混物力学性能的研究

考察了硫黄用量和聚合物共混比对动态硫化ＥＰＤＭ／ＰＰ热塑性弹性体性能的影响。结果表明,随着硫黄用量增大,ＥＰＤＭ／Ｐ共混物的拉伸强度、１００％定伸应力和扯断伸长率先增大后减小、硬度有所增大,随着ＰＰ用量的增大,ＥＰＤＭ／ＰＰ共混物的拉伸强度、１００％定伸应力和硬度均有所增大,扯断伸长率也先大后减小。ＰＰ用量的变化对这些性能的影响更显。     

聚丙烯／三元乙现橡胶共混体系的研究

研究了三元乙丙橡胶（ＥＰＤＭ）对聚丙烯（ＰＰ）结晶行为的影响以及ＰＰ／ＥＰＤＭ共混物的形态与性能的关系。ＥＰＤＭ对ＰＰ的熔点、结晶温度无明显影响，ＰＰ／ＥＰＤＭ共混物的结晶度随ＥＰＤＭ组份含量的增加而降低，适量的ＥＰＤＭ可使ＰＰ的晶体尺寸减小，晶胞参数与组份比无关。当ＥＰＤＭ用量为３０％￣４０％时，共混物的冲击强度迅速提高。     

动态硫化PP／EPDM性能对共混工艺的依赖及其机理研究

本文通过对一步法和母料法两种共混工艺制备的动态硫化ＰＰ／ＥＰＤＭ力学性能、拉伸形变特性,熔体流动行为,交联程度和微观结构等的表征和分析,研究了动态硫化ＰＰ／ＥＰＤＭ性能对共混工艺的依赖及其作用机理。结果显示,在保证有效地提高材料加工流动性的前提下,母料法能有效地抑制动态硫化中ＰＰ的降解,提高ＥＰＤＭ的交联程度,粒度均匀性和分散均匀性,从而强化材料的增韧效果以及其它力学性能,并提高材料性能的均匀性。     

PP/HDPE/EPDM共混物的研究

研究了聚丙烯（ＰＰ）、高密度聚乙烯（ＨＤＰＥ）和ＥＰＤＭ共混制备非交联型ＰＰ／ＨＤＰＥ／ＥＰＤＭ三元共混物。结果表明，当共混比ＰＰ／ＨＤＰＥ／ＥＰＤＭ＝６５／２０／１５，活性碳酸钙为３０份，ＨＤＰＥ品种为ＧＦ７７５０，采用先把ＨＤＰＥ和ＥＰＤＭ预制成混料再与ＰＰ共混的方法，可得到性能良好的ＰＰ／ＨＤＰＥ／ＥＰＤＭ共混物。     

EVM/NBR动态硫化共混物性能的研究

研究了橡胶型乙烯醋酸乙烯酯共聚物（ＥＶＭ）／ＮＢＲ共混比、硫黄和叔丁基酚醛树脂（２４０２树脂）硫化体系对共混物性能的影响，并对比了动态硫化和静态硫化共混物在性能上的差异。试验结果表明，ＥＶＭ／ＮＢＲ共混比显著影响共混物的力学性能，而采用ＮＢＲ预先动态硫化的方法后，共混物胶料的挤出口型膨胀率明显减小，老化性能得到改善，同时减弱了硫黄和２４０２树脂等硫化体系对ＥＶＭ硫化的影响，使多种硫化体系可以共存于共混物中。ＤＳＣ分析表明ＥＶＭ／ＮＢＲ动态硫化共混物只有一个玻璃化温度，且介于ＥＶＭ和ＮＢＲ之间，说明ＥＶＭ和ＮＢＲ具有良好的相容性。     

乙苯,苯乙烯的生产及合成乙苯,苯乙烯催化剂的研究进展

苯乙烯是重要的石油化工原料。本文介绍了国内外苯乙烯生产的发展概况，合成乙苯，苯乙烯所用的催化剂种类，并就苯乙烯生产及催化剂的发展趋势提出了自己的观点。     

Synthesis and characterization of homopolymers and copolymers of various acrylates and acrylonitrile

Various homopolymers and copolymers of methyl acrylate, ethyl acrylate, butyl acrylate, and acrylonitrile in different feed ratios were synthesized. These were characterized by IR, ¹³C-NMR, DSC, DTA, and TGA. Spectroscopic characterization helped in differentiating copolymers of different mol ratios. Thermal analysis revealed different degradation patterns for homopolymers and copolymers. The temperature and energy changes associated with various phase transitions were dependent on the chemical composition of homo- and copolymers, as expected. © 1993 John Wiley & Sons, Inc.     

生物质气化及生物质与煤共气化技术的研发与应用

总结了生物质原料的特点及生物质单独气化的缺点;介绍了国内外生物质气化技术及生物质与煤共气化技术的研发与应用现状;分析了在此领域国内外的发展趋势与前景;概括了开展生物质与煤共气化技术研发的意义。     

Electronic structures and reactivities of monometallic and bimetallic clusters of Au and Cu

The variation of the Au 4f binding energy of Au clusters with the cluster size has been established by measuring the binding energies of clusters whose size distributions were independently determined by HREM and STM. The binding energy increases significantly when the cluster size is less than 2 nm. Au-Cu bimetallic clusters of the composition Cu₃Au have been deposited for the first time on carbon substrates. The shifts in the core level binding energies of the bimetallic clusters show the effect of alloying in the case of large clusters, but show effects of both alloying and cluster size in the case of the small clusters. The interaction of CO with Cu₃Au clusters is stronger than with a bulk Cu metal. The interaction of CO with small Cu clusters also seems to be stronger than with bulk Cu or with large Cu clusters.     

钾盐资源及钾肥供需情况分析及预测

阐述了国内外钾盐资源及钾肥生产现状,对国内外钾盐的供需形势进行了分析及预测,从资源、原材料、国际市场三方面提出了解决我国钾盐短缺的措施。     

Kinetics and Mechanism of Oxidation of Mono- and Polyacetals

Abstract

Kinetics and mechanisms of oxidation of 6 acetals by molecular oxygen and ozone in liquid phase have been studied. Reaction with molecular oxygen (70°C, 15–16 hr) leads to the formation monoethers of the corresponding glycols with 68–90% selectivity. Salts of metals and complexes with crown-ethers have increased the reaction rate significally. Ozone have reacted with acetals with formation similar products. The mechanisms of intermediate stages have been proposed.     

Comparison of the Adhesion and Cohesion of Triblock and Random Copolymers of Styrene and Butadiene

A substantially greater detachment energy is required to strip a polyethylene tereph-thalate (Mylar) film from a styrene-butadiene-styrene (SBS) triblock copolymer compared to that for peeling from a random styrene-butadiene (SBR) copolymer. This is true even though the intrinsic interaction between the Mylar and each elastomer is expected to be similar because of their virtually identical chemical composition. It is proposed that this difference in peel strength (between the SBS and SBR) is a consequence of the much higher dissipative capacity of the former elastomer. Another manifestation of this is the higher cohesive tear strength of the SBS compared to the SBR. Extents of energy dissipation within each elastomer during detachment of the Mylar adherend are consistent with the hypothesis that the average maximum stress experience before detachment is some similar fraction of each elastomer's tensile strength.     

Wetting properties of homopolymers and copolymers of pentafluorostyrene and methylacrylate and homopolymer blends

Polypentafluorostyrene (PPFS), polymethylacrylate (PMA), and poly(pentafluorostyrene-co-methylacrylate), poly(PFS-co-MA) were prepared and the wetting characteristics of polymer blends of PPFS and PMA were compared with that of poly(PFS-co-MA) via contact angle measurements. The critical surface tension of polypentafluorostyrene was found to be 22.6 dyne/cm, which is comparable to the value reported for polytrifluoroethylene (22 dyne/cm). The critical surface tension of poly(PFS-co-MA) is not linearly related to its composition. The polymer blends of PPFS and PMA exhibit significant surface enrichment of the fluoropolymer. The harmonic-mean method¹ was employed to determine surface tensions of these polymers and many known polymers. It is found that the method produces useful surface tension data provided the contact angle values are derived from testing liquids of dissimilar polarity.     

责任和责任心的涵义与结构

责任是人应主动承担的角色义务和对其因过失所造成后果应承担的责罚.有两层涵义:一是义务;二是后果.责任心是个体自觉做好分内事务和履行道德义务的心理倾向,是个性心理品质成分中自我特征维度上的重要内容.责任心具有两个方面的涵义:一是角色分内职责;二是角色道德义务.责任心是一种通过责任认知、责任个性和责任适应的动态形式表现出来的静态品质,责任心是责任心过程结构与责任心关系结构相互制约、相互影响的统一体.     

二甲基二烯丙基氯化铵和丙烯酰胺的合成及应用

用复合引发体系(过硫酸盐-偶氮类引发剂)和脂肪胺类氧化还原体系引发,在实验室获得了单体转化率≥98%,特性粘数高于13.6 dL/g的阳离子共聚物PDA,探讨了控制聚合物分子量的影响因素.