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Reinforcement of flexible nylon-6 by using poly (m-phenylene isophthalamide) PmIA (Nomex) using (MDI) 4,4-diphenylene methane diisocyanate as a chain extender was studied. Observation by scanning electron microscopy showed that the multiblock copolymer had a homogeneous texture. From the differential scanning calorimetry measurements, the multiblock copolymers were shown to have only one melting point, T
m, which is higher than that of nylon-6. The wide-angle X-ray diffraction pattern shows that nylon-6 has two diffraction peaks at 2=20° and 23.8°. However, the multiblock copolymer has only one peak at 2=20°, indicating a different crystal structure of multiblock copolymers. The copolymers appear to have a significant reinforcing effect on the mechanical properties. 相似文献
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Hou Hongbo Pu Zejun Liu Xueyu Li Xianyong He Xiaohang Liu Jingyue Zhong Jiachun 《Journal of Materials Science: Materials in Electronics》2021,32(16):21441-21449
Journal of Materials Science: Materials in Electronics - In this work, ferroferric oxide (Fe3O4) microspheres with a diameter of?~?150 nm were in situ grown on the surface of... 相似文献
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Nylon-6 was reinforced by two semi-rigid aromatic polyamides, poly(p-diphenylmethyl terephthalamide) (PMA), and poly(p-diphenyloxide terephthalamide) (POA), and also one wholly-rigid aromatic polyamide, poly(m-phenylene isophthalamide) (PmlA) by physical blending and chemical copolymerization usingp-amino phenyl acetic acid (P-APA) as a coupling agent. From the results of differential scanning-calorimetry, it was shown that both the polyblends with semi-rigid and wholly-rigid polyamides exhibited a glass transition temperature,Tg, higher than that of nylon-6 homopolymer. It also showed that theT
gs of wholly-rigid polyblends were higher than those of semi-rigid polyblends. Nevertheless, the multiblock copolyamides appeared to have even higherT
g andT
m, and better thermal stability. Morphological observations revealed that all the polymer alloys (polyblends and copolymers) were a dispersed phase structure, although the multiblock copolyamides were more homogeneous and compatible. Based on wide-angle X-ray diffraction, it was found that the polyblends had two diffraction peaks, i.e. 2 = 20.5 ° and 24 °. However, the multiblock copolyamides had only one peak at 2 = 20 °, evidently indicating a new crystal structure of the multiblock copolyamides formed. For the mechanical properties, it was found that the multiblock copolyamides had a more significant reinforcing effect than those of polyblends, especially those copolymerizing with wholly aromatic polyamides. 相似文献
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An oxidized edge surface of pyrolytic graphite (PG) has been prepared by electrochemical treatment. A thin layer of poly(vinyl chloride) (PVC) was coated on the oxidized edge surface, and the PVC-coated sample heat treated at 300, 400, and 500 °C, respectively. The influence of the PVC coating on the structural change of the oxidized edge surface of PG caused by the heat treatment was studied by laser Raman and Fourier transform-infrared attenuated total reflection spectroscopies. For the electrochemical treatment, the formation of oxygen-containing functional groups proceeds over the edge surface of PG. With increasing degree of oxidation, the functional groups are formed in the following order; hydroxyl groups, carboxyl groups, lactone groups, quinones, and acid anhydrides. Acid anhydrides are formed on the outermost surface and completely eliminated by heat treatment up to 300 °C. The other functional groups remain even after heat treatment up to 500 °C. However, the functional groups are eliminated by the PVC coating, the elimination temperature depending on the type of functional groups: quinones, lactone groups, and carboxyl groups are eliminated at 300, 400, and 500 °C, respectively. PVC coated on the edge surface is found to play an important role in the complete elimination of oxygen-containing functional groups with >C=O through heat treatment at 500 °C. 相似文献
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The structure of o!igo (caprolactone glycol)-based polyurethane-poly(vinyl chloride) (PVC) blends obtained from tetrahydrofuran solution was studied by X-ray diffraction and electron microscopy. The system is characterized by a oornp!ex phase diagram with two types of equilibria: (1) crystal-liquid equilibrium in the region of blend compositions up to 40 wt% PVC; (2) liquid-liquid equilibrium in the region of man compositions. The crystallization kinetics of oligo(caprolactone) polyurethane blocks from an initially compatible amorphous blend was investigated. Small-angle X-ray cattering (SAXS) studies provide evidence that the amorphous component (PVC) is incorporated in the interlamellar crystalline regions of the compositions. The amorphous blends are characterized by the presence of modulated structures at two scale levels, this being explained as e result of the process in which the bulk samples were obtained from a three-component polymer-polymer-solvent system. 相似文献
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Linear poly(ethylene oxide)-based polyurethane hydrogels: polyurethane-ureas and polyurethane-amides
P. Petrini M. C. Tanzi C. R. Moran N. B. Graham 《Journal of materials science. Materials in medicine》1999,10(10-11):635-639
Over the last 30 years, water-swellable and water-insoluble hydrogels have been extensively investigated and developed, leading to a large family of materials which have found uses in a wide range of biomedical applications. While hydrogels usually present a crosslinked structure, linear polyurethane-ureas (PUUs) based on poly(ethylene oxide) have been shown to be able to absorb and swell with aqueous media without dissolving. This behavior is due to the phase separated domain morphology, where hydrogen bonded urethane/urea hard segment domains are dispersed in a PEO soft segment domain. This work investigates the possibility of obtaining linear poly(ethylene oxide)-based polyurethane-amide (PUA) hydrogels using two amide diols as chain extenders, a mono amide diol (AD) and a diamide diol (DD), and a dicarboxylic acid (maleic acid, MA). Poly(ethylene oxide) based PUAs were obtained using a “one-shot” bulk polymerization technique. The chemicophysical characterization and water-solubility tests showed that these materials, while having molecular weights similar to the PUUs, do not possess sufficient phase separation, hydrogen bonding and hydrophobicity of the hard segment domains to exhibit hydrogel behavior. Crosslinked PUAs using maleic acid as chain extender show interesting hydrogel properties. © 1999 Kluwer Academic Publishers 相似文献
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肝素化水性聚氨酯改性医用聚氯乙烯表面的研究 总被引:3,自引:0,他引:3
以N 甲基二乙醇胺为扩链剂合成了阳离子水性聚氨酯 (ACPU) ,将其固定在医用聚氯乙烯管内壁并对其进行肝素化。通过全血凝固时间实验证明 ,改性后的医用聚氯乙烯管的抗凝血性明显提高。另外使用红外光谱分析了阳离子水性聚氨酯的结构及其肝素化处理后聚合物结构的变化 ,并考察了MDEA含量对阳离子水性聚氨酯乳液及其涂膜性能的影响。 相似文献
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Fracture toughness of exponential layer-by-layer polyurethane/poly(acrylic acid) nanocomposite films
E. Kheng P. Podsiadlo A.K. Kaushik E.M. Arruda 《Engineering Fracture Mechanics》2010,77(16):3227-3245
This paper characterizes the fracture toughness of layer-by-layer (LBL) manufactured thin films with elastic polyurethane, a tough polymer, and poly(acrylic acid) as a stiffening agent. A single-edge-notch tension (SENT) specimen is used to study mode I crack propagation as a function of applied loading. Experimental results for the full-field time histories of the strain maps in the fracturing film have been analyzed to obtain R-curve parameters for the nanocomposite. In particular, by using the strain maps, details of the traction law are measured. A validated finite strain phenomenological visco-plastic constitutive model is used to characterize the nanocomposite film while a discrete cohesive zone model (DCZM) is implemented to model the fracture behavior. The LBL manufactured nanocomposite is found to display a higher fracture toughness than the unstiffened base polymer. 相似文献
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Jing SUN Lu YAO Qiao-Ling ZHAO Jin HUANG Rui SONG Zhi MA Ling-Hao HE Wei HUANG Yong-Mei HAO 《材料科学前沿(英文版)》2011,5(4):388
The crystallization modification of poly(vinylidene fluoride) (PVDF) was investigated for the blend films of PVDF and poly(methyl methacrylate) (PMMA). The mass crystallinity (χ c) and further, the β-phase content (F (β)) of PVDF, were studied for the as-prepared blend films with different mass ratios. In addition, the variations of χ c and F (β) were systematically probed once the PMMA component was removed from the related blend systems. DSC, FTIR and XRD measurements all indicated that 1) χ c, F (β) and even the content of α-phase (F (α)) decreased with the addition of PMMA; 2) with the extraction of PMMA, both χ c and F (β) increased while F (α) decreased. It is worth noting that the increase of χ c and F (β) depended on the relative amount of extracted PMMA (E PMMA), i.e., the more PMMA was removed, the more χ c and F (β) increased. These results reveal the hindrance effect from the PMMA constituent to the crystallization of PVDF, and consequently, this restriction would be released when the PMMA was extracted. 相似文献
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Wu Zecheng Zhang Zhijun Wei Wei Yin Yanqing Huang Chongxing Ding Jiang Duan Qingshan 《Journal of Materials Science》2022,57(9):5456-5466
Journal of Materials Science - Poly (lactic acid)/thermoplastic polyurethane (PLA/TPU) ductile fibrous porous material was obtained by electrospinning, which has better mechanical properties than... 相似文献