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1.
从理论上详细分析了非相容共混体系液滴形变、破碎的机理和双重海/岛复合结构的形成条件.应用电子显微镜和光学显微镜法,以聚苯乙烯/等规聚丙烯共混物为试样,对聚合物共混中双重海/岛复合结构的形成机理、结构形态和形成条件进行了研究.提出了双重海/岛复合结构形成过程的模型.  相似文献   

2.
对LDPE/CPE/炭黑三相复合导电体系的亚微形态和导电性能进行了研究。实验发现,该体系的亚微形态在共混比LDPE/CPE大于和小于50/50时为典型的“海-岛”结构,在50/50时,为两相连续交错“互锁”结构;在共混比大于50/50时,LDPE/CPE炭黑复合体系的导电性能较单一的LPDPE树脂与炭黑复合体系的高2-5个数量级。  相似文献   

3.
PBT/PC共混体系流变性能与形态结构研究   总被引:1,自引:0,他引:1  
采用毛细管流交仪测定了PBT/PC共混物的表观粘度、剪切应力,观察了不同共混物组成和不同温度下共混物的流变行为,并借助扫描电镜对共混物和微观形态结构进行分析。结果表明:PBT/PC熔体共混物的流变行为接近假塑性流体.温度对共混物的流变行为影响很大,共混物的熔体粘度在PBT/PC为90/10和60/40时呈双极值.共混物为两相结构,PC含量为4-50%时呈两互锁结构。  相似文献   

4.
多相高分子共混物熔体中微区的发展机理,决定着体系的最终相结构.所以研究共混物熔体或溶液中的微区聚结机理已越来越显得重要和必要.作者先前的研究工作表明[1~6],通过简单共混得到的均匀共混体系(如PP/EVAc),在一定的退火热处理条件下,会自组织形成梯度相结构,即分散相粒子尺寸及其浓度从样品中心到表面逐渐增大.作者认为,这一结构的形成主要与基板对共混体系粗化过程的影响作用有关.初步认为是由于体系分散相聚结过程中,共混组分对基板的选择性浸润析出而导致了这种特殊的结构,亦可称为基板诱导相结构的形成.…  相似文献   

5.
ABS/PVC共混体系的相容性,力学性能和形态   总被引:7,自引:0,他引:7  
通过掺和各种橡胶聚合物如ABS、MBS和天然橡胶等,使聚氯乙烯(PVC)的低抗冲击强度和难加工性得到改进「‘,’‘.ABS和PVC的共混物具有优异的抗冲击强度、刚性、韧性和耐化学性等.这与两聚合物的组份比、相容性及形态结构密切相关“,“.将丙烯睛(SAN)共聚单体引人聚苯乙烯(陀)和丁二烯(孤)后,使*踞/**C具有好的相容性D’.本文对*踞”*C共混体系的不同共混组份,同一共混条件下的相容性,力学性能和形态结构进行了研究.ABS(通用型301树脂,兰州化学工业公司);PVC-SG-3型(吉林化学工业公司),稳定剂…  相似文献   

6.
报道了对嵌段共聚物结晶型共混体系结晶行为的研究.通过对聚甲基丙烯酸甲酯-聚四氢呋喃两嵌段共聚物/聚四氢呋喃共混体系的研究,我们发现1.微相分离结构的存在,可使相容的这类体系形成多种特殊的结晶形态;2.共混体系的相容性可以方便地由其结晶行为来判断;3.共混体系中共聚物的结晶能力显著提高.这些特点都明显不同于一般的聚合物共混体系.  相似文献   

7.
马宇  王军佐 《应用化学》1996,13(5):25-28
用WAXD、SEM及力学性能测试等研究热致液晶/PEEK/嵌段共聚物三元共混体系形态、结构和性能。结果表明嵌段共聚物的加入,使体系具有一定的相容性和较好的界面粘接,共混物的强度、模量有一定的提高,对共混物的结晶行为具有明显的影响,当热致液晶含量高时,基材与液晶两相间出现明显的分离现象,即“皮-芯”结构.  相似文献   

8.
聚苯乙烯/顺丁橡胶共混过程中的相结构   总被引:3,自引:0,他引:3  
利用激光背散射装置结合密炼机对聚合物共混过程进行了在线分析.以典型完全不相容体系聚苯乙烯/顺丁橡胶为共混体系,对不同共混速度下结构参数随共混时间及共混条件如剪切速率等的变化进行了详细讨论.利用扫描电镜与激光背散射在线分析对聚合物共混过程结构参数变化进行了比较,结果显示聚苯乙烯/顺丁橡胶共混物处于熔融态与处于固态时结构基本相同.  相似文献   

9.
应用DSC、偏光显微镜和动态力学分析,研究了胆甾液晶与甲基丙烯酸甲酯-甲基丙烯酸丁酯无规共聚物共混体系的相容性及相态转变.表明共聚物的组成、分子量大小可抑制胆甾液晶的相态转变.给出了形成稳定相容的液晶/高分子体系的最佳条件.  相似文献   

10.
采用二甲基硅氧烷-b-乙二醇嵌段共聚物(DMS-b-OE)对聚二甲基硅氧烷/聚氨酯(PDMS/PU)共混体系的增容,重点研究了增容共混体系的微观形态结构和软科学性能之间的关系。扫描电子显微镜、动态力学分析和力学性能测试结果表明:DMS-b-OE对PDMS/PU具有优良的增容作用,改善了PDMS/PU共混体系的相容性,提高了该共混物的力学性能。其抗张强度由3.4MPa提高到7.6MPa。  相似文献   

11.
Oriented thermoplastic polyurethane (TPU) fiber and fiber network were first prepared by electrospinning. The as-prepared TPU fiber or fiber network was then pre-fixed in poly(lactic acid) (PLA)/TPU composite to improve the toughness of PLA. For comparison purpose, TPU/PLA composites with sea-island morphology were also prepared by traditional solution blending and mechanical blending. The results show that the toughness of PLA is greatly increased by the special pre-fixed oriented TPU fibers even at a low content, and the toughness is further increased by the TPU fiber network. Our results indicate for the first time that the toughening effect of special TPU fibers or fiber network is much better than that of traditional TPU with sea-island morphology. This study provides guidance to largely improve the toughness of PLA by designing the special phase morphology of TPU.  相似文献   

12.
冯玉红  张若愚 《高分子科学》2014,32(8):1099-1110
Polylactide (PLA) was successfully toughened by blending with bio-based poly(ester)urethane (TPU) elastomers which contained bio-based polyester soft segments synthesized from biomass diols and diacids. The miscibility, mechanical properties, phase morphology and toughening mechanism of the blend were investigated. Both DSC and DMTA results manifested that the addition of TPU elastomer not only accelerated the crystallization rate, but also increased the final degree of crystallinity, which proved that TPU has limited miscibility with PLA and has functioned as a plasticizer. All the blend samples showed distinct phase separation phenomenon with sea-island structure under SEM observation and the rubber particle size in the PLA matrix increased with the increased contents of TPU. The mechanical property variation of PLA/TPU blends could be quantitatively explained by Wu's model. With the variation of TPU, a brittle-ductile transition has been observed for the TPU/PLA blends. When these blends were under tensile stress conditions, the TPU particles could be debonded from the PLA matrix and the blends showed a high ability to induce large area plastic deformation before break, which was important for the dissipation of the breaking energy. Such mechanism was demonstrated by tensile tests and scanning electron microcopy (SEM) observations.  相似文献   

13.
制备了一种新型聚丙烯 丁苯橡胶 纳米碳酸钙三元纳米复合材料 .研究结果显示 ,复合材料中的大多数纳米碳酸钙粒子被包藏在丁苯橡胶中 ,并与之共同形成分散于聚丙烯树脂中的分散相 ,这种聚丙烯纳米复合材料具有高刚性、高韧性、高耐热性和高的结晶速率 .系统研究了成核剂苯甲酸钠的加入和纳米碳酸钙的用量对该类纳米复合材料相态结构、结晶形态和结晶动力学的影响 ,以及具有包藏结构的分散相粒径和PP中β晶含量对材料性能的影响 .结果表明 ,苯甲酸钠的加入和纳米碳酸钙用量的提高均可使体系中分散相粒径减小 ,结晶速率加快 ,进而使材料的韧性、刚性和耐热性提高 .  相似文献   

14.
All-organic composites are widely used in energy storage application due to the high breakdown strength performance, but the improvement of energy storage was limited by the relatively low dielectric constant. Therefore, to satisfy the high demands of dielectric materials, energy storage properties of polymer composites should be further enhanced. In this article, poly(vinylidene fluoride-co-chlorotrifluoroethylene) (P(VDF-CTFE)) and polyurea (PUA), which are known as high dielectric ferroelectric material and linearly high energy storage efficiency material respectively, are composited through double layer (DL) casting method for the first time. The properties of DL structured composite film is contrasted with solution blending structure especially in energy storage efficiency, and the results demonstrate that DL structure design can make great use of advantages of two materials and also can avoid the influence of phase separation between P(VDF-CTFE) and PUA efficiently. Moreover, high breakdown strength (6180 kV/cm) and high energy storage efficiency (77%) of DL composites can be realized simultaneously by incorporating PUA as an insulating layer, and the mechanism is discussed in detail. This work provides an effective route to improve the energy storage properties of polymer dielectric materials and shows great application potential.  相似文献   

15.
The formation of the structure and properties of mesoporous composite ceramics based on an ASD-1 aluminum powder and commercial adsorbent powders (zeolites and active alumina) was studied. It was found that the mechanism of the formation of contacts between the particles of commercial adsorbents and aluminum is analogous to the mechanism of synthesis of an Al(OH)3/Al composite. The dissolution of aluminum and the precipitation of the hydroxo complexes of aluminum from solution to the region of interparticle contacts are responsible for this mechanism. The resulting composite ceramics exhibited a polydisperse pore structure and high values of mechanical strength, gas permeability, and thermal conductivity; it can be used as a block adsorbent and catalyst support.  相似文献   

16.
Applications of blood purification membranes are fuelled by diverse clinical needs, such as hemodialysis, hemodiafiltration, hemofiltration, plasmapheresis, and plasma collection. For clinical usage, the adding of polyvinylpyrrolidone (PVP) is the general protocol for the design of antifouling and antithrombotic properties integrated artificial membranes. In the present work, to insight into the detailed surface properties and blood compatibilities of the PVP blended composite membranes, we synthesized a series of PVP polymers with different molecular weights using reversible addition fragmentation chain transfer polymerization and designed a series of polyethersulfone (PES)/PVP composite membranes by a physically blending method. The effects of PVP molecular weights and blending ratios on the surface properties and the blood compatibilities of the composite membranes were investigated in detail. The surface attenuated total reflection Fourier transform infrared spectra and scanning electron microscopy pictures indicated that the PVP was successfully immobilized into the membranes, and the composite membranes exhibited morphology transformation from finger‐like structure to sponge‐like structure, which indicated that the composite membrane had tunable porosity and permeability by adding PVP. The blood compatible tests revealed that the composite membranes showed increased hydrophilicity, decreased plasma protein adsorption, suppressed platelet adhesion, and prolonged blood clotting time compared with pristine PES membrane. These results indicated that the PES/PVP composite membranes exhibited enhanced antifouling and antithrombotic properties than the pristine PES membrane. Meanwhile, the results also suggested that the composite membranes with larger molecular weight PVP and higher blending ratios might show better blood compatibility. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

17.
聚丙烯酸铅/环氧树脂辐射防护材料的制备及性能研究   总被引:3,自引:0,他引:3  
采用γ辐射接枝聚合法制备了纳米聚丙烯酸铅/环氧树脂辐射防护材料,利用傅立叶变换红外光谱仪(FTIR)、X射线衍射谱仪(XRD)、透射电镜(TEM)和扫描电镜(SEM)对其结构进行了分析,利用材料万能试验机测量了拉伸性能和三点弯曲性能,利用多道γ谱仪测量了屏蔽性能.结果表明,复合材料为两相聚合物共混体系,其分散形态呈明显的海-岛结构.聚丙烯酸铅微球粒径约为5nm,具有一定的结晶,微球表面连接环氧树脂分子形成三维网状结构.复合材料特殊结构使其韧性和强度较纯环氧树脂有明显的提高,其断口呈现一定的韧性断裂的特征,对γ射线的质量吸收系数高于铅的质量吸收系数,是一种屏蔽性能十分突出的轻质材料.  相似文献   

18.
采用在苯乙烯 (St)悬浮聚合过程中滴加甲基丙烯酸甲酯 (MMA)乳液聚合组分的悬浮 乳液复合聚合方法 ,制备大粒径聚苯乙烯 聚甲基丙烯酸甲酯 (PS PMMA)复合粒子 .研究聚合物粒径分布和颗粒形态的变化发现 ,在St悬浮反应中期滴加MMA乳液聚合组分后 ,聚合体系逐渐由悬浮粒子与乳胶粒子并存向形成单峰分布复合粒子转变 ,最终形成核 壳结构完整的大粒径PS PMMA复合粒子 ;在St悬浮反应初期滴加MMA乳液聚合组分 ,St与MMA一起分散成更小液滴 ,反应后期凝并成非核 壳结构复合粒子 ;在St悬浮反应后期滴加MMA乳液聚合组分 ,PMMA乳胶粒子与PS悬浮粒子基本独立存在 .根据以上结果 ,提出了St MMA悬浮 乳液复合聚合的成粒机理 .  相似文献   

19.
IntroductionMagnetite (Fe3O4) is widespread in the environ-ment although it is thermodynamically unstable with re-spect to hematite(α-Fe2O3) in the presence of oxygen.It has been widely used for targeted delivery ofdrugs[1], in MRI reagents[2], hyperther…  相似文献   

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