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1.
不同蒙脱石的有机插层及聚合剥离   总被引:2,自引:0,他引:2  
以成因、类型、性质不同的6种蒙脱石为原料,制备了有机插层和聚酰胺6/蒙脱石纳米复合材料。研究了蒙脱石矿物类型、成分及阳离子交换容量对其有机插层及聚合剥离的影响。结果表明:有机插层蒙脱石层间距随插层剂用量及阳离子交换容量的增加而增加,低阳离子交换容量及高钠含量蒙脱石更有利于插层剥离。钠化对蒙脱石有机插层影响不明显。  相似文献   

2.
于晓波  王刚  蒋巍  董薇 《弹性体》2011,21(6):65-70
综述了橡胶/粘土插层纳米复合材料的制备方法及性能特征。重点介绍了溶液插层法、乳液插层法和熔体插层法及相关研究进展。评价了各种制备技术的优缺点,提出了橡胶/粘土插层纳米复合材料的发展趋势。  相似文献   

3.
聚合物/纳米粘土插层复合材料的研究进展   总被引:1,自引:0,他引:1  
综述了插层法制备聚合物/纳米粘土复合材料的新进展。根据插层机理和方法的差别,插层法主要分为溶液插层和熔融插层两类、总结了使用二次插层和乳液聚合制备聚合物基纳米复合材料的新方法,展望了聚合物/纳米粘土复合材料的开发及应用前景。  相似文献   

4.
聚羧酸减水剂在粘土中的吸附、插层行为会对水泥混凝土的性能产生影响.综述了聚羧酸减水剂在粘土中的吸附行为及在粘土矿物蒙脱石中的插层行为的机理、性能表征及对水泥净浆凝结时间、流动度、抗压强度;水泥胶砂流动度、抗压强度、抗折强度;混凝土和易性、坍落度、抗压强度的影响,总结了粘土与聚羧酸减水剂对水泥混凝土性能影响的评价方法,阐述了调控插层行为的措施,展望了调控聚羧酸减水剂插层行为的研究前景.  相似文献   

5.
插层法制备聚合物/粘土纳米复合材料的原理   总被引:8,自引:2,他引:8  
介绍了聚合物/粘土纳米复合材料的插层方法、制备原理和工艺过程,探讨了纳米复合材料微观结构的影响因素,概述了聚合物/粘土纳米复合材料的形成机理。  相似文献   

6.
有机插层剂对粘土/EPDM纳米复合材料性能的影响   总被引:2,自引:0,他引:2  
研究了一种新型有机插层剂对双羟基烷基季铵盐蒙脱土/EPDM纳米复合材料性能的影响.结果发现,以双羟基烷基季铵盐处理粘土,在高温高转速熔融共混后,所得到的EPDM硫化胶具有优异的力学性能.X射线衍射发现,形成的粘土/EPDM纳米复合材料为剥离型结构.  相似文献   

7.
本文对近年来关于熔融插层法制备聚合物/粘土纳米复合物(PCN)过程中成型加工影响作用的研究进展进行了综述。介绍了不同加工设备对制备PCN的不同影响,并指出双螺杆挤出机是进行熔融混合的最合适的加工设备。概述了停留时间、螺杆结构等加工条件和不同成型工艺对制备PCN的不同作用。并对今后的研究提出了展望。  相似文献   

8.
高岭石有机插层复合材料的研究及应用现状   总被引:1,自引:0,他引:1  
崔超  邵珊 《佛山陶瓷》2008,18(5):36-40
高岭石是一种层状硅酸盐矿物,有机物可进入其层间形成高岭石有机插层复合物。本文综述了高岭石有机插层复合物的发展及其制备,分析了高岭石插层复合物的插层反应特点和插层影响因素,并概述了该领域目前的研究重点和应用前景。  相似文献   

9.
不同工艺有机插层蛭石的制备及表征   总被引:5,自引:2,他引:5  
韩炜  张尧  刘炜  吴驰飞 《硅酸盐学报》2006,34(1):98-101
以2倍蛭石阳离子交换容量的十六烷基三甲基溴化铵为插层剂,利用热液搅拌法、球磨法、煮沸法、熔融搅拌法等4种不同工艺对蛭石进行插层处理.对有机插层后的蛭石进行了粉晶X射线衍射、Fourier变换红外光谱和热重分析表征.结果表明:不同插层工艺会导致有机插层蛭石的层间距及微结构的变化.随着层间距的增大,蛭石层间的有机相含量逐渐增大.  相似文献   

10.
熔融插层制备聚合物/层状粘土纳米复合材料研究进展   总被引:13,自引:0,他引:13  
从流变性能、加工操作过程对熔融插层制备聚合物纳米复合材料的影响、分散机理的研究进展等方面对熔融插层制备聚合物 /层状粘土进行了综述 ,并对今后的研究提出了展望。  相似文献   

11.
朱建君  李安琪 《广州化工》2010,38(5):166-168
蒙脱土在聚丁二烯(端羟基聚丁二烯和端羧基聚丁二烯)中能自发分散剥离形成纳米复合材料,以X-射线衍射(XRD)和透射电子显微镜(TEM)等方法观察了这种纳米复合材料的微观结构。重点研究了液体橡胶的端官能团和蒙脱土层间有机改性剂的烷基链长对蒙脱土片层在液体橡胶中剥离的影响,同时总结出蒙脱土在聚丁二烯液体橡胶基体中的剥离机理。  相似文献   

12.
Fully exfoliated PS/clay nanocomposites were prepared via FRP in dispersion. Na‐MMT clay was pre‐modified using MPTMS before being used in a dispersion polymerization process. The objective of this study was to determine the impact of the clay concentrations on the monomer conversion, the polymer molecular weight, and the morphology and thermal stability of the nanocomposites prepared via dispersion polymerization. DLS and SEM revealed that the particle size decreased and became more uniformly distributed with increasing clay loading. XRD and TEM revealed that nanocomposites at low clay loading yielded exfoliated structures, while intercalated structures were obtained at higher clay loading.

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13.
采用预聚法合成了以端羟基聚丁二烯(HTPB)和聚己内酯二醇(CAPA2200)为软段、2,4-甲苯二异氰酸酯(TDI-100)和3,5-二甲硫基甲苯二胺(DADMT)为硬段的聚氨酯弹性体。研究了预聚体中HTPB与CAPA2200的质量比、NCO含量、扩链系数等因素对聚氨酯弹性体力学性能的影响。结果表明,当NCO质量分数为3.8%、HTPB与CAPA2200质量比为25∶75、扩链系数为0.90时,弹性体的生热较小,综合性能较好。  相似文献   

14.
Summary: Vinylester resin matrix composites were fabricated with 1, 3, 5 and 10 wt.‐% loadings of organoclay. The composite samples were subjected to various characterization techniques like X‐ray diffraction, flexural testing, dynamic mechanical analysis, thermogravimetric analysis, and scanning electron microscopy. The clay samples as well as the clay–resin composites were investigated by X‐ray diffraction. From the shift in the peak positions and the change in d‐spacing values, it was evident that there was intercalation in the 10 wt.‐% composites, whereas exfoliation occurred in the 1, 3, and 5 wt.‐% composites. The flexural strength and the breaking energy of all the composites were decreased compared with the unfilled resin, but there was an increase in flexural modulus value by 13%. From the dynamic mechanical analysis of the 3 and the 5 wt.‐% composites, it was observed that the loss modulus value was higher in the 3 wt.‐% composites, but the glass transition temperature was slightly higher in the 5 wt.‐% composites. Thermal degradation behavior was also improved in the 5 wt.‐% composites compared with the 3 wt.‐% composites.

Fracture surface of 3 wt.‐% clay filled vinylester resin matrix composite in different magnifications.  相似文献   


15.
羟丁型聚氨酯的应用概述   总被引:2,自引:0,他引:2  
简要介绍了端羟基聚丁二烯(HTPB)的发展概况和羟丁型聚氨酯的特点,重点介绍了以端羟基聚丁二烯、TDI预聚物等为主要原料制备的羟丁型聚氨酯在弹性体、密封剂、胶粘剂、电绝缘材料和防水材料等方面的应用。  相似文献   

16.
环氧化端羟基聚丁二烯增韧环氧树脂的研究   总被引:1,自引:0,他引:1  
使用环氧化端羟基聚丁二烯(EHTPB)对双酚A型环氧树脂进行增韧改性。对EHTPB增韧的固化产物及端羟基聚丁二烯(HTPB)增韧的固化产物进行力学性能测试,运用差示扫捕量热法测试同化产物的玻璃化转变温度,采用扫面电镜观察树脂增韧前后的断面形貌,显示为韧性断裂。各种结果表明,EHTPB对环氧树脂的增韧效果优于HTPB,该增韧剂的加入能够在不明显降低树脂强度的条件下,大幅度提高体系韧性的同时保持树脂的玻璃化转变温度。  相似文献   

17.
二茂铁甲酸原位接枝环氧化端羟基聚丁二烯的合成研究   总被引:1,自引:0,他引:1  
选用四丁基溴化铵作相转移催化剂,进行二茂铁甲酸(FcCA)接枝环氧化端羟基聚丁二烯(EHTPB)的合成研究.合成产物的红外光谱和1H-NMR显示,在1714和1276 cm-1处表现出明显的羧酸酯基团特征吸收峰,在1139和823 cm-1处表现出茂环特征吸收峰,在4.2~4.9处显示茂环上9H的核磁共振谱带.化学分析...  相似文献   

18.
介绍了核磁共振(NMR)研究端羟基聚丁二烯(HTPB)中羟基类型的进展,给出了自由基聚合法合成HTPB中涉及的反应机理,总结了HTPB的羟基类型和力学性能的相互关系,并为解决HTPB指标相同、批次不同而性能有很大差异的问题提供了一个基本思路和方法。  相似文献   

19.
The preparation of new rubber based nanocomposites by using properly modified organophilic clays is described. A commercial organophilic montmorillonite containing a hydroxylated ammonium ion is reacted with LPBs. The reaction causes a decrease of the polarity of the clay and a great increase of the interlayer distance. The modified organoclays are successfully dispersed into rubber matrices (SBR or BR) by melt blending in an internal batch mixer. SAXS analyses and TEM micrographs revealed the formation of highly exfoliated nanocomposites containing intercalated stacks made of few lamellae.

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20.
Influence of polyurethane (PU) structure on the nature of PU/clay nanocomposite was studied using varying amounts of trimethylol propane (TMP) as branching agent. The effect of hydroxyl groups in the modifier of organoclays on the structure of PU/clay nanocomposites was studied. Nanocomposites were characterized using wide‐angle X‐ray diffraction measurements (WAXD) and transmission electron microscopy (TEM). The results show that formation of completely exfoliated and well dispersed polyurethane/clay nanocomposites via in situ polymerization, is facilitated by the presence of tethering groups on the clay surface and an ability to form branched and crosslinked structures. Incorporation of long alkyl chains in addition to tethering hydroxyl groups in the modifier structure of the clay did not significantly improve the compatibility of linear PU with the clay. Intercalated thermoplastic polyurethane/clay nanocomposites, prepared using poly(caprolactone diol) as soft segment and isophorone diisocyanate and 1,4‐butanediol as hard segments show increase in storage tensile moduli at temperatures before glass transition temperature when functional groups capable of chemically reacting with the growing polymer chains are present in the clay modifier. This is indicative of improved interaction of the polymer with the clay surface when the modifier has larger number of hydroxyl groups. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010  相似文献   

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