PVC/CPE共混物的加工温度与性能关系

厦门大学化学系用差示扫描量热法（仍C）、透射电镜（＊＊M）和扫描电镜（亚M）等技术研究了PVC／CPE共混物的加工温度、相容性与共混制品性能的关系。研究表明，CPE与PVC有部分相容性，使共混物中存在网状结构，从而提高制品的抗冲击强度。但当加工温度低于165C或高于195C时，CPE不能形成网状结构，因而抗冲击强度降低。PVC/CPE共混物的加工温度与性能关系     

HNBR/EVA共混物力学性能、耐热氧老化和耐油性能的研究

将氢化丁腈橡胶（HNBR）和乙烯-醋酸乙烯酯共聚物（EVA）按不同配比制成共混物，考察不同配比下共混物的物理机械性能、耐热氧老化性能和耐非极性燃料油和石油的性能。结果表明，随EVA用量的增加，共混物的物理机械性能有所提高，加工流动性有所改善；当EVA用量大于30份，且使用温度高于50℃时，共混物机械性能下降较大：随HNBR用量的增加，共混物的耐热氧老化和耐油性能有明显提高。     

POM／COPA二元及POM／COPA／EVA三元共混物的研究

研究了聚甲醛供聚酰胺（POM/COPA）二元及聚甲醛／共聚酰胺／乙烯-醋酸乙烯酯共聚物（POM／COPA／EVA）三元共混物，探讨了COPA、EVA用量对共混体系性能的影响。结果表明，C1DPA的加入使共混物的熔融温度（Tm）增大；当COPA含量为4％（质量分数，下同）时，00PA能够较均匀地分散于POM基体中，共混物缺口冲击强度出现最大值，比纯聚甲醛提高了约63．3％，而拉伸强度变化不大，POM／COPA共混物具有较理想的综合力学性能。EVA的加入使共混物缺口冲击强度和拉伸强度均呈下降趋势。     

乙烯—醋酸乙烯酸共聚物对茂金属聚乙烯的改性研究

以添加不同比例的茂金属聚乙烯（mLLDPE）/乙烯-醋酸乙烯酯（EVA）共混物为研究对象，考察了EVA含量对mLLDPE/EVA共混物的力学性能，热性能，流变性能，动态力学性能和形态结构的影响，研究结果表明，EVA添加到mLLDPE中，增加了mLLDPE的剪切敏感度，降低了mLLDPE的熔融粘度，改善了mLLDPE的流动性和加工性，在一定的添加比例范围内mLLDPE和EVA具有很好的相容性，可以在改善mLLDPE加工性能，引入极性基团的同时又保持与纯mLLDPE相近的力学性能，但会导致共混物材料的刚性下降，柔性增加，热分析数据说明，mLLDPE/EVA共混体系中，在EVA含量较小时共混物存在大量共晶，与mLLDPE有很好的相容性，无论是熔融曲线还是降温曲线都只出现一个峰，当EVA含量增大时，mLLDPE/EVA共混物出现相分离，曲线出现双峰，但两峰值呈现靠近趋势，预示mLLDPE/EVA共混物中仍存在少量共结晶。     

EVA／木质素薄膜的制备与性能研究

研究了经造粒、吹塑成膜的乙烯醋酸乙烯酯共聚物（EVA）／木质素共混物的结构、热性能以及力学性能。热重分析表明木质素与EVA共混物的热稳定性比单一组分的高；差示扫描量热分析表明木质素与EVA的相容性好；傅里叶红外光谱分析表明木质素与EVA之间存在分子间氢键相互作用；扫描电子显微分析表明木质素含量对共混物形貌有明显的影响；力学性能测试表明木质素含量在30％（质量分数，下同）以内，共混物薄膜仍具有较好的力学性能，随着木质素含量的增加，共混物力学性能降低。     

聚氯乙烯与乙烯—醋酸乙烯共聚物和氯化聚乙烯的共混改性

通过扭辨分析来测定聚氯乙烯(PVC)与乙烯——醋酸乙烯酯共聚物(EVA)的相溶性;通过应力——应变曲线来表征PVC与EVA和氯化聚乙烯(CPE)共混物力学性能的变化。为PVC共混物的工业生产提供理论上的参考依据。     

PVC/EVA共混物的研究

中国科学院化学所对PVC与EVA共混物的性能进行了研究。该所用醋酸乙烯含量48％的EVA与PVC进行共混的动力学和微观性能研究表明，PVC与EVA共混物中存在的半相容性。当EVA体积含量18％～80％时，共混物的性能随EVA含量增加而变化；当EVA含量6％“8％时，共混物的抗冲击强度改进最为明显。PVC/EVA共混物的研究     

EVA熔体流动速率对PLA/EVA共混物性能的影响

通过熔融共混法制备了聚乳酸（PLA）/乙烯-乙酸乙烯酯共聚物（EVA）共混物,采用SEM、DSC、旋转流变仪等研究了VA质量分数为28%,熔体流动速率（MFR）不同的EVA对PLA/EVA共混物性能的影响。结果表明,EVA熔体流动速率越小,其在PLA基体中分散越均匀,EVA颗粒粒径也越小。共混物的结晶度随EVA熔体流动速率的增大而增大,但PLA的玻璃化转变温度（Tg）基本不受EVA的影响。PLA/EVA共混物的复数黏度和储能模量均随EVA的熔体流动速率的增高而减小。力学性能测试结果表明,当EVA的质量分数为15%时,PLA的断裂伸长率明显升高,冲击强度约是纯PLA的2倍。     

热缩型硅橡胶复合绝缘子的研制

研究了乙烯醋酸乙烯共聚物（EVA）、硅橡胶（PDMVS）和氢氧化铝不同配比时所组成的共混物的力学性能和电学性能及辐射交联对EVA／KPDMVS共混物的凝胶含量和力学性能的影响规律，确定了适合的辐交联剂量及利用该共混物制备热缩型硅橡胶复合绝缘子的工艺条件。     

聚烯烃弹性体增韧改性聚碳酸酯的研究

用四种聚烯烃弹性体对聚碳酸酯（PC）进行了增韧改性。探讨了不同种类和用量的增韧剂对聚合物共混物力学性能的影响。结果表明，EVA的加入使共混物韧性改善最明显，当其用量为15％时，材料的缺口冲击强度提高至38．7kJ／m^2，为纯PC的25倍，但材料的拉伸强度急剧下降。POE—g—MAH对PC的增韧效果仅次于EVA，但共混物的拉伸强度降低程度比EVA小，且共混物的断裂伸长率提高很多。其它两种共混体系PC／EAA、PC／LLDPE-g—MAH的性能介于EVA和POE—g—MAH之间。综合考虑材料的各种机械性能，添加20％的POE—g—MAH的PC共混物的性能较佳。     

国内PVC共混改性研究的最新进展

介绍了近年来国内PVC共混改性的研究状况,重点阐述了PVC/丙烯腈-丁二烯-苯乙烯（ABS）、PVC/甲基丙烯酸甲酯-丁二烯-苯乙烯（MBS）、PVC/氯化聚乙烯（CPE）、PVC/乙烯-醋酸乙烯酯（EVA）等几种共混体系研究的最新进展。     

Water-Swellable Thermoplastic Vulcanizates Based on Ethylene-vinyl Acetate Copolymer/Cross-linked Sodium Polyacrylate/Chlorinated Polyethylene

A novel water-swellable rubber (WSR) was prepared by dynamically vulcanizing ethylene-vinyl acetate copolymer (EVA)/chlorinated polyethylene (CPE) blends where the cross-linked poly (sodium acrylate) (CPNaAA) was used as a super water-absorbent resin and dispersed in the CPE rubber. Experimental results showed that the mechanical properties of TPVs decreased while the water-swelling ratio increased significantly with increasing of CPNaAA dosages, the swelling ratio of 60 phr CPNaAA TPVs reaching 746.1% at 93 h. Morphological study showed that the CPNaAA particles were dispersed randomly in the TPVs; Some significant gaps and large cavities could be found in the surface of dried TPVs.     

Radiation effects on LDPE/EVA blends

Radiation effects of low‐density polyethylene/ethylene‐vinyl acetate copolymer (LDPE/EVA) blends were discussed. EVA content in the LDPE/EVA blends was an enhancement effect on radiation crosslinking of LDPE/EVA blends, and the highest radiation crosslinking was obtained when the EVA content was reached at 30% when irradiated by γ‐ray in air. The phenomenon was discussed with the compatibility, morphology, and thermal properties of LDPE/EVA blends and found that the enhanced radiation crosslinking of the LDPE/EVA blends was proportional to the good compatibility, the increasing degree of the amorphous region's content of the LDPE/EVA blends, and the vinyl acetate content of EVA. We also found that the vinyl acetate of EVA in the blends is easily oxidized by γ‐ray irradiation in air. The possible radiation crosslinking and degradation mechanism of LDPE/EVA blends was discussed quantitatively with a novel method “step‐analysis” process of irradiated LDPE/EVA blends in the thermal gravimetric analysis (TGA) technique. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1296–1302, 2002     

动态交联PP/EVA共混物的制备与性能研究

本文将动态交联技术应用于PP/EVA共混体系中,制得动态交联PP/EVA共混物。采用Hakke转矩流变仪研究了动态交联对PP/EVA共混物扭矩的影响;研究了DCP和EVA含量对共混物力学性能的影响;考察了动态交联共混物的维卡软化点。结果表明：加入DCP后,PP/EVA共混物扭矩先升后降,DCP的添加量为EVA含量的1%为宜。随EVA用量的增加,动态交联EVA/PP共混物的冲击强度大幅提高,但拉伸强度有所降低。少量经动态交联的EVA颗粒可以促进共混物中PP的结晶, 提高共混物的维卡软化点。     

Toughening effects of ethylene–vinyl acetate copolymers with different vinyl acetate content and viscosity on nylon 1010 blends

Nylon 1010 blends with ethylene–vinyl acetate copolymer (EVA) and maleated ethylene–vinyl acetate (EVA‐g‐MAH) were prepared through melt blending. The vinyl acetate (VA) content and viscosity of EVA significantly affected the notched impact strength of nylon/EVA/EVA‐g‐MAH (80/15/5) blends. The nylon/EVA/EVA‐g‐MAH blends with high notched impact strength (over 60 kJ/m²) were obtained when the VA content in EVA ranged from 28 to 60 wt%. The effect of VA content on the notched impact strength of blends was related to the glass transition temperature for EVA with high VA content and crystallinity for EVA with low VA content. For nylon blends with EVA with the same VA content, low viscosity of EVA led to high notched impact strength. Fracture morphology of nylon/EVA/EVA‐g‐MAH (80/15/5) blends showed that blends with ductile fracture behavior usually had large matrix plastic deformation, which was the main energy dissipation mechanism. A relationship between the notched impact strength and the morphology of nylon/EVA/EVA‐g‐MAH (80/15/5) blends was well correlated by the interparticle distance model. POLYM. ENG. SCI., 2009. © 2009 Society of Plastics Engineers     

Radiation effects on HDPE/EVA blends

In this article, we discuss the radiation effects of high‐density polyethylene (HDPE)/ethylene–vinyl acetate (EVA) copolymer blends. In comparison with the low‐density polyethylene/EVA blends, the EVA content in the HDPE/EVA blends had a lower enhancement effect on radiation crosslinking by γ‐ray irradiation in air. The phenomenon is discussed with the compatibility, morphology, and thermal properties of HDPE/EVA blends. The HDPE/EVA blends were partly compatible in the amorphous region, and radiation crosslinking of the HDPE/EVA blend was less significant, although increasing the amorphous region's content of the HDPE/EVA blends and the vinyl acetate content of EVA were beneficial to radiation crosslinking. The good compatibility was a prerequisite for the enhancement effect of EVA on the radiation crosslinking of the polyethylene/EVA copolymer. The radiation crosslinking and the degradation mechanism of HDPE/EVA blends were examined quantitatively by a novel method, the step analysis process of irradiated HDPE/EVA blends with a thermal gravimetric analysis technique. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 553–558, 2002     

Study on segmental interaction parameter between ethylene and vinyl acetate monomer units of EVA by inverse gas chromatography

A method of analysis of inverse gas chromatography (IGC) measurements on copolymers to calculate segmental interaction parameters was proposed. Poly(ethylene‐co‐vinyl acetate) (EVA), poly(vinyl acetate) (PVAc), and dotriacontane (C32) were studied at 120°C with eight different probes of varying polarities by IGC. The value of the segmental interaction parameter between ethylene units and vinyl acetate units in EVA was found to be 1.18, which is consistent with the literature values. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 693–698, 1999     

Radiation effects on poly(propylene) (PP)/ethylene–vinyl acetate copolymer (EVA) blends

Radiation effects on poly(propylene)/ethylene–vinyl acetate copolymer (PP/EVA) blends are discussed. Increasing the EVA content enhanced the crosslinking effect of radiation in PP/EVA blends. This effect was significant when the EVA content was ≥50% in PP/EVA blends that were exposed to γ‐ray irradiation in air. This phenomenon is discussed in relation to the compatibility, morphology, and thermal properties of PP/EVA blends. The results indicate that the effect is dependent on the compatibility, the increase in the amorphous region content, and the EVA content in PP/EVA blends. The possible mechanism of radiation crosslinking or degradation in irradiated PP/EVA blends was studied quantitatively by a novel method, a “step analysis” process, and thermal gravimetric analysis. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 3420–3424, 2002     

A Fourier transform infra-red study of the phase behaviour of polymer blends. Ethylene-vinyl acetate copolymer blends with poly(vinyl chloride) and chlorinated polyethylene

Fourier transform infra-red studies of ethylene-vinyl acetate (EVA) blends with poly(vinyl chloride) (PVC) and chlorinated polyethylene (CPE) are presented. Previous studies have demonstrated that these blends are compatible at ambient temperature and exhibit lower critical solution temperatures (LCST) in a range that is readily accessible and below the onset of significant polymer degradation. Infra-red spectra of EVA-PVC and EVA-CPE films cast from solution and recorded at room temperature exhibit the familiar frequency shifts and band broadenings of the carbonyl stretching vibration that are consistent with compatible blend systems. Significantly, at temperatures above the LCST, these spectral features are not observed, which implies phase separation. By monitoring the frequency of the EVA carbonyl stretching vibration in samples of the blends, an estimation of the relative strength of the intermolecular interactions has been obtained as a function of temperature. A non-linear relationship is observed and the temperature at which the relative strength of the intermolecular interaction appears very weak correlates with the LCST. The implications of these results are discussed.