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首页> 外文期刊>Applied clay science >Synthesis and characterization of PMMA and organic modified montmorilonites nanocomposites via in situ polymerization assisted by sonication
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Synthesis and characterization of PMMA and organic modified montmorilonites nanocomposites via in situ polymerization assisted by sonication

机译:超声辅助原位聚合合成PMMA和有机改性蒙脱土纳米复合材料及其表征

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摘要

A variety of organo-modified montmorillonite (OMMT) and poly(methylmethacrylate) (PMMA) nanocomposites (CPN) were synthetized by in situ polymerization in a chloroform solution under probe sonication at clay loadings of 3 mass%. A factorial experimental design was used to study the effects of the synthesis variables: Flory-Huggins (F-H) interaction parameters between PMMA and clay organomodifier (three grades of OMMT) and sonication energy (26.0 kJ, 30.3 kJ and 34.6 kJ), aiming clay dispersion at nanoscale levels into the polymeric matrix and improvements in CPN properties. The distinct surfactant side groups of commercial OMMT were: hydroxyl (C30B), aryl (C10A) or alkyl (C25A), considering their similar interlayer space. Multiple techniques of analysis to evaluate the level of clay dispersion were used. Small-amplitude oscillatory shear rheology (SAOS) indicated a high level of clay dispersion for the PMMA/C25A CPN and a tendency to form a percolated network structure from the low shear thinning exponent n(omega) of complex viscosity, either at low (n(omega) = -0.97) or high (n(omega)= -0.83) sonication energy. However, the rheological results showed a low level of clay dispersion for PMMA/C10A (n(omega) = -0.70) and PMMA/C30B (n(omega) = - 0.40). The F-H interaction parameter was the statistically significant factor for the shear thinning exponent n(omega) response. X-ray diffraction (XRD) of CPN exhibited no discernible reflections for PMMA/C25A-26 kJ and PMMA/C10A-30.3 kJ CPN, suggesting that a high level of clay dispersion was achieved. Transmission electronic microscopy (TEM) images of PMMA/C25A-36.4 kJ and PMMA/C3OB-26 kJ CPN showed exfoliated/intercalated and intercalated morphologies, respectively. Thermogravimetry presented a significant increase in PMMA chain scission temperature of up to 82 degrees C for all CPN when compared to pristine PMMA. The UV-visible transmittance of PMMA/C25A-26 kJ CPN showed to be around 4.5% lower in comparison with pristine PMMA. The CPN refractive index showed a slight reduction, which could even candidate them for new materials in optical electronic devices. The improvements in the verified properties for PMMA/C25A CPN were attributed to the lower F-H interaction parameter of C25A alkyl surfactant with chloroform when considering the others OMMT side groups. The chemical affinity of the alkyl chain to the chloroform could contribute to the diffusion of the solvent/monomer solution into the interlayer space of the clay, prior to polymerization, and then the polymer chain growth to push the layers apart.
机译:在氯仿溶液中,在3%的粘土含量下,通过探头超声处理,通过原位聚合合成了各种有机改性的蒙脱土(OMMT)和聚甲基丙烯酸甲酯(PMMA)纳米复合材料(CPN)。使用析因实验设计研究合成变量的影响:PMMA与粘土有机改性剂(三种等级的OMMT)之间的Flory-Huggins(FH)相互作用参数和超声能(26.0 kJ,30.3 kJ和34.6 kJ),瞄准粘土在纳米级分散到聚合物基质中,并改善了CPN性能。考虑到它们相似的层间空间,商业OMMT的不同表面活性剂侧基为:羟基(C30B),芳基(C10A)或烷基(C25A)。使用多种分析技术来评估粘土的分散程度。小振幅振荡剪切流变学(SAOS)表示PMMA / C25A CPN的粘土分散度高,并且在低粘度(n)下,由复数粘度的低剪切稀化指数n(ω)形成渗透网络结构的趋势。 Ω= -0.97)或高(nΩ= -0.83)的超声能。但是,流变学结果表明,对于PMMA / C10A(nΩ= -0.70)和PMMA / C30B(nΩ=-0.40),粘土的分散度较低。 F-H相互作用参数是剪切稀疏指数n(ω)响应的统计学显着因素。 CPN的X射线衍射(XRD)对PMMA / C25A-26 kJ和PMMA / C10A-30.3 kJ CPN没有明显的反射,表明获得了高水平的粘土分散性。 PMMA / C25A-36.4 kJ和PMMA / C3OB-26 kJ CPN的透射电子显微镜(TEM)图像分别显示了脱落/嵌入和嵌入的形态。与原始PMMA相比,热重法显示所有CPN的PMMA断链温度均显着提高,最高可达82摄氏度。与原始PMMA相比,PMMA / C25A-26 kJ CPN的紫外线可见透射率降低了约4.5%。 CPN折射率略有降低,甚至可以将它们用作光学电子设备中的新材料。当考虑其他OMMT侧基时,PMMA / C25A CPN的已验证性能的改善归因于C25A烷基表面活性剂与氯仿的较低F-H相互作用参数。在聚合之前,烷基链对氯仿的化学亲和力可能有助于溶剂/单体溶液扩散到粘土的层间空间中,然后使聚合物链增长以将各层推开。

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