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辐射接枝法生产离子交换纤维的进展 总被引:4,自引:0,他引:4
介绍了辐射接枝生产离子交换纤维的主要方法 :共辐射接枝法、无氧预辐射接枝法和有氧预辐射接枝法。比较了这些方法的优缺点 ,指出有氧预辐射接枝更适合于工业化生产。对今后辐射接枝生产离子交换纤维的发展进行了展望 相似文献
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无机微粒表面接枝聚合改性进展 总被引:1,自引:0,他引:1
讨论了表面接枝改性机理,综述了"接枝到"(Grafting to)法和"由表面接枝"(Grafting from)法以及其它表面接枝改性方法的研究进展。 相似文献
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聚丙烯固相接枝马来酸酐改性研究 总被引:1,自引:0,他引:1
采用固相法以马来酸酐对聚丙烯粒料(粒径为2.7 mm)进行接枝改性,研究了反应条件对接枝率和接枝效率的影响,通过化学分析、红外光谱、平衡转矩等对接枝聚丙烯进行了表征。结果表明,马来酸酐成功接枝于聚丙烯上,最大接枝率可达2.2%;马来酸酐接枝聚丙烯平衡转矩明显大于接枝空白样,接枝率的大小对平衡转矩影响不大。 相似文献
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A normalized and universally applicable calibration function for the Fourier‐transformed infrared (FTIR) quantification of the glycidyl methacrylate (GMA) grafting yield in polymers of known compositions having ethylene block sequences was established. The 1H nuclear magnetic resonance (1H‐NMR) spectroscopy results achieved on different GMA‐grafted ethylene/propylene/diene rubber (EPDM‐g‐GMA) and ethylene/GMA copolymers were correlated to their FTIR data to calibrate the relative determination of the FTIR method. Both direct and indirect standardization approaches were followed and evaluated. The calibration deduced was used to investigate the free radical grafting reaction of GMA on EPDM rubber in the melt phase. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 2616–2624, 1999 相似文献
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利用反应挤出技术制备了低密度聚乙烯(LDPE)/亚甲基丁二酸接枝物。研究了引发剂种类及用量对接枝率和接枝物熔体流动速率(MFR)的影响。结果表明:采用引发剂L-101的接枝率最高,添加ω(L-101)为0.2%时.接枝率即可接近90%,接枝的同时伴有交联,接枝物的MFR从LDPE的16g/10min下降到2g/10min左右。 相似文献
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简单介绍了甲基丙烯酸缩水甘油酯熔融接枝聚烯烃的第二单体、引发剂、反应温度和反应时间等因素对接枝反应的影响,探讨了接枝率的测定方法及接枝聚烯烃在塑料改性中的应用等。 相似文献
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简单介绍了甲基丙烯酸缩水甘油酯(GMA)熔融接枝聚烯烃的第二单体、引发剂、反应温度和反应时间等因素对接枝反应的影响,接枝率的测定方法及接枝聚烯烃在塑料改性中的应用等。 相似文献
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Rohini Agarwal Sahil Chandrakant Kalambe Pampi Chakraborty Subhendu Ray Chowdhury Harish Jagat Pant 《应用聚合物科学杂志》2024,141(5):e54871
Ethylene propylene diene elastomer (EPDM) harbors diverse microbiota that form biofilms. Such biofilms may contaminate water and can increase drag force impacting the hydrodynamic performance of a ship, once it is used as fenders. Here, the EPDM surface is modified by radiation-assisted grafting to prevent biofilm formation. Three different monomers, namely, methacrylic acid (MAA), isodecyl methacrylate (IDM), and lauryl methacrylate (LMA), are grafted on EPDM. The modified surfaces are characterized by Fourier transform infrared (FTIR) spectroscopy, surface wettability, mechanical and dynamic mechanical properties (DMA), and scanning electron microscopy (SEM). The modified surfaces are subjected to biofouling by prominent biofilm adherents, that is, Pseudomonas aeruginosa and Klebsiella pneumoniae. The standard plate count and resazurin fluorescence assays are performed to observe the microbial load on these surfaces. The MAA-grafted EPDM, which is hydrophilic in nature, shows a considerable decrease in bacterial adhesion compared to pure EPDM, but for IDM and LMA-grafted EPDM, it is the opposite. The deterioration of the surface with bacteria by environmental scanning electron microscopy (ESEM) supports the findings. The tensile property of the modified EPDM is observed to be within satisfactory limits. After such modification, the EPDM is expected to expand its application. 相似文献
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三元乙丙橡胶与尼龙树脂的增容共混 总被引:2,自引:0,他引:2
以甲基丙烯酸缩水甘油酯为接枝单体、过氧化二异丙苯为引发剂对三元乙丙橡胶(EPDM)进行熔融接枝。用傅里叶红外光谱(FTIR)对接枝产物进行了表征,分析测试了共混硫化胶的力学性能和微观结构。结果表明,随着共混体系中接枝EPDM用量的增加,EPDM与尼龙树脂的相容性不断改善,尼龙颗粒作为分散相在EPDM中分散得更加均匀和细致化,共混硫化胶的力学性能得到进一步提高,尼龙树脂原位生成的短纤维可明显提高共混硫化胶的撕裂强度,同时使其保持了弹性体高伸长率的特性。 相似文献
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采用双螺杆熔融接枝的方法,在引发剂过氧化二异丙苯(DCP)作用下,将甲基丙烯酸缩水甘油酯(GMA)和共单体苯乙烯(St)接枝到聚丙烯(PP)上。通过傅立叶变换红外光谱仪确定了接枝物的生成,采用酸碱滴定法测定了接枝率。探讨了GMA,St,DCP不同用量对PP接枝物的接枝率和熔体流动速率的影响,并将接枝产物PP–g–(St–co–GMA)加入PP/尼龙6(PA6)的合金中,通过注塑成型样条,测定其力学性能,并观察微观结构。结果表明,St的加入能够提高接枝率,抑制副反应的发生。在PP/PA6合金中加入接枝物PP–g–(St–co–GMA),其拉伸强度可提高46.45%,弯曲强度可提高32.47%,但对冲击强度影响不大。 相似文献
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Free‐radical melt‐grafting of the dual‐monomer systems glycidyl methacrylate–styrene (GMA‐St) and hydroxyethyl methacrylate–styrene (HEMA‐St) onto polypropylene (PP) has been studied using a single‐screw extruder. For single monomer grafting systems, degradation of PP was unavoidable and deterioration of the mechanical properties of the grafted PP subsequently occurred because of β‐scission of PP chains during the free‐radical melt‐grafting process. However, for the dual‐monomer systems, it is shown that the addition of styrene as a comonomer can significantly enhance the GMA or HEMA grafting levels on PP and reduce the extent of β‐scission of PP backbone. It has been found that the grafting degree of dual‐monomer melt‐grafted PP, such as PP‐g‐(GMA‐co‐St) or PP‐g‐(HEMA‐co‐St), is about quadruple that of single‐monomer grafted PP for the same monomer and dicumyl peroxide concentrations. Moreover, the melt flow rate of the dual‐monomer grafted PP is smaller than that of the unmodified PP. Hence, PP not only was endowed with higher polarity, but also kept its good mechanical properties. © 2000 Society of Chemical Industry 相似文献