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利用正丁基锂(n-BuLi)与炭黑(CB)表面含氧基团反应制得了表面含-OLi基团的反应型炭黑,以该炭黑与聚氧乙烯-聚氧丙烯-聚苯乙烯(PEO-PPO-PS)多嵌段聚合物组成的阴离子引发体系作活性中心,研究了苯乙烯在炭黑表面的阴离子接枝聚合。FT-IR,TEM和DSC分析表明在接枝炭黑表面存在苯乙烯的聚合物。接枝炭黑在甲苯中有良好的分散稳定性。 相似文献
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丙烯酰胺在炭黑表面接枝聚合研究 总被引:4,自引:0,他引:4
利用Ce^4+和羟甲基化炭黑组成的氧化还原引发体系,探讨了丙烯酰胺在炭黑表面的自由基水溶液接枝聚合机理。研究表明:单体浓度、硝酸浓度和铈盐用量直接影响丙烯酰胺在炭黑表面的接枝聚合,FTI和TEM分析证明:改性炭黑表面存在着聚丙烯酰胺。改性炭黑粒子的Zeta电位值与未改性炭黑粒子相同,但它与水组成的分散体具有极好的分散稳定性。 相似文献
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丙烯酸甲酯在炭黑表面的接枝聚合及水解 总被引:1,自引:0,他引:1
在炭黑表面接枝聚合物 ,可提高其在相应介质中的分散性[1] .乙酰丙酮合锰可以有效地引发羊毛、纤维素、淀粉等天然高分子的接枝聚合 [2~ 4 ] ,季君晖 [5]将其与羟甲基化炭黑组成引发体系 ,引发了甲基丙烯酸甲酯、丙烯酸丁酯、苯乙烯等单体在炭黑表面进行接枝聚合 .但该体系难以引发水溶性的单体 ,因此得到的接枝炭黑只能用于油性体系 .目前制备亲水性接枝炭黑大多采用 Ce4 +/羟甲基化炭黑引发体系 ,该体系对 O2 特别敏感 ,反应条件相当苛刻 .本文采用乙酰丙酮合锰与羟甲基化炭黑组成引发体系 ,引发丙烯酸甲酯在炭黑表面的接枝聚合 .在 Na… 相似文献
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交联聚乙烯醇(CPVA)微球表面含有大量的羟基,具有良好的生物相容性。在水溶液体系中利用这些羟基,与铈盐构成氧化还原引发体系,实施了甲基丙烯酸(MAA)的表面引发接枝聚合,制备了接枝微球CPVA—g—PMAA,考察了主要因素对接枝聚合的影响。采用红外光谱(FT—IR)及扫描电子显微镜(SEM)对接枝微球进行了表征。结果表明,羟基-铈盐氧化还原引发体系可有效地引发MAA在CPVA微球的表面接枝聚合,当铈盐浓度为4.9×101mol/L、硫酸浓度为0.17mol/L、反应温度为45。C、单体浓度为0.54mol/L时,每1。0g接枝微球CPVA—g—PMAA可接枝PMAA30g。 相似文献
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超声引发自由基聚合制备聚苯乙烯磺酸钠接枝炭黑 总被引:1,自引:0,他引:1
通过在超声环境下,单体苯乙烯磺酸钠发生自由基聚合,生成的聚合物长链自由基被炭黑表面捕获,制备聚合物接枝炭黑.借助红外光谱、热重、粒度、透射电镜和zeta电位分析对该接枝炭黑进行表征.同时研究超声条件对接枝率的影响.结果表明,单体聚合并接枝到炭黑表面,同时炭黑的附聚体和一些大的聚集体结构被超声破碎,平均粒径大为减小;在300W超声波输出功率下,反应1h后,接枝率达到12.8%并趋于稳定.由于接枝分子链上磺酸基的存在,接枝炭黑在水中的分散稳定性显著改善. 相似文献
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丙烯酸乙酯在炭黑表面的阴离子接枝聚合研究 总被引:2,自引:0,他引:2
丙烯酸乙酯在炭黑表面的阴离子接枝聚合研究蒋子铎,刘长生,刘安华,吴璧耀(武汉化工学院精细化工系武汉430073)关键词炭黑,丙烯酸乙酯,阴离子聚合,接枝聚合由于炭黑粒子自聚力强,存在难分散、易絮凝的特点,影响其在高分子材料中的分散和分散稳定性.对此国... 相似文献
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通过正丁基锂(BL)引发甲基丙烯酰氧丙基纳米氧化硅(MAMSN)与苯乙烯共聚,制备了聚苯乙烯表面接枝纳米氧化硅(PS—g—Silica),并考察了正丁基锂加入量对苯乙烯转化率(C)、接枝率(PG)以及聚苯乙烯分子量(Mn)的影响。实验结果表明,阴离子聚合可以获得比自由基聚合更大的分子量和更高的转化率以及接枝率。 相似文献
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《European Polymer Journal》1985,21(2):195-199
Grafting of N-vinyl pyrrolidone onto gelatin is reported using α,α'-azobisisobutyronitrile as initiator. The effects of various variables like initiator concentration, monomer concentration, time and temperature are reported. These variables appreciably affect the percentage grafting, grafting efficiency and molecular weight of the grafted chain. The graft copolymers were characterized by i.r. spectroscopy and ninhydrin tests. Sulphathiazole was coupled to these graft copolymers using a diazotization technique. Blood compatibility of these graft copolymers of different side chain molecular weight was found to be satisfactory. 相似文献
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《高分子科学杂志,A辑:纯化学与应用化学》2013,50(1-2):129-143
ABSTRACT A novel redox system, potassium diperiodatonickelate [Ni (IV)]‐chitosan, was employed to initiate the graft copolymerization of methyl acrylate (MA) onto chitosan in alkali aqueous solution. The effects of reaction variables such as monomer concentration, initiator concentration, reaction time, pH and temperature were determined. By means of a series of copolymerization, the grafting conditions were optimized. The maximum grafting percentage obtained was 404.1% when 0.3 g chitosan was copolymerized with 1.8 mL monomer at 35°C for 5 hours with [Ni (IV)]=9.4×10?4 M and the total volume was 20 mL. Ni (IV)-chitosan system is found to be an efficient redox initiator for this graft copolymerization. A single electron transfer mechanism is proposed to explain the formation of radicals and the initiation. The grafted copolymers were characterized by IR and X-ray diffraction diagrams. The thermal stability of chitosan and chitosan-g-PMA was studied by thermogravimetric analysis (TGA). 相似文献
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Jacob John Jian Tang Zhihong Yang Mrinal Bhattacharya 《Journal of polymer science. Part A, Polymer chemistry》1997,35(6):1139-1148
Polycaprolactone-graft-maleic anhydride (PCL-g-MA) copolymer was prepared by grafting maleic anhydride onto PCL in a batch mixer and in an extruder using dicumyl peroxide as the initiator. The graft content was determined with the volumetric method by converting the anhydride functions to acid groups and then titrating with ethanolic potassium hydroxide. The grafted polymer was extracted with xylene to remove any unreacted monomer before the estimation step. The effect of temperature and the various concentrations of the initiator and monomer used for the grafting reaction were investigated. The presence of residual initiator in the reaction product was checked using thin-layer chromatography. Molecular weight determination was carried out for the pure and grafted polymer using gel permeation chromatography to determine if chain scission was present. Results indicate that maleic anhydride is grafted onto PCL using free radical initiators. The grafting reaction was confirmed by FTIR and NMR techniques. FTIR spectra showed absorption bands around 1785 and 1858 cm−1. NMR spectra gave signals for methine proton at 3.47 ppm. For a given peroxide level, a higher temperature or residence (reaction) time gave higher percentage of grafted MA. There was an optimum temperature and initiator concentration after which the percentage of MA grafted on PCL decreased. The number-average molecular weight, tensile strength, and the percent elongation of PCL-g-MA were comparable to those of PCL before grafting. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 1139–1148, 1997 相似文献
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Photoinitiated graft copolymerization of acrylamide onto chitosan under heterogeneous conditions and in the absence of a photo initiator was investigated. The effect of irradiation time, the amount of chitosan and monomer concentration on the extent of grafting was examined. The maximum grafting percentage obtained was 294%. The copolymer was characterized using carbon-13 nuclear magnetic resonance (13C-NMR) spectroscopy, X-ray diffraction analysis (XRD), differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). The system designed allows synthesis of grafted chitosan with free amine groups which are otherwise possible only by chemical protection. The swelling properties of copolymer were followed in aqueous solution. 相似文献
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铬酸引发丙烯酸正丁酯与淀粉接枝共聚反应 总被引:6,自引:0,他引:6
作为淀粉改性方法之一 ,不饱和酸及其酯与淀粉接枝共聚反应是一个较新的研究领域 ,其中以 Ce4 +离子作为引发剂的较多[1,2 ] ,也有用Mn3+-H2 SO4 体系 [3]和 Mn[( H2 P2 O7) 3]3-引发体系的[4 ] 。铬酸是一种具有强氧化性的强酸 ,虽然它单独存在时并不引发乙烯类单体的聚合 ,有报道[5] 铬酸可以引发丙烯腈与苎麻纤维素接枝共聚 ,淀粉和纤维素同属于碳水化合物。本文对铬酸引发丙烯酸正丁酯与淀粉接枝共聚反应进行了研究 ,考察了反应条件对接枝反应的影响。1 实验部分1 .1 原料可溶性淀粉 (北京奥特生物技术责任有限公司 ) ,丙烯酸正丁… 相似文献
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R. Mani M. Bhattacharya J. Tang 《Journal of polymer science. Part A, Polymer chemistry》1999,37(11):1693-1702
Maleic anhydride (MAn) was grafted onto aliphatic and aromatic/aliphatic copolyesters by reactive extrusion in the presence of a free radical initiator using a twin‐screw extruder. The grafting reaction was confirmed by spectroscopic analyses. The presence of succinic anhydride groups was shown by FT‐IR spectroscopy, and NMR spectra indicate that the grafts consist of single succinic anhydride units. The 2D 1H‐NMR spectra (COSY) indicate that grafting reactions take place at aliphatic dicarboxylic acid units of copolyesters. The graft content was determined by a nonaqueous titration method. The effects of concentration of initiator and monomer and reaction temperature on the graft content and intrinsic viscosity were studied. The low percentage grafting in poly(lactic acid) was observed due to the presence of limited free radical sites in the polymer backbone. Temperature and monomer and initiator concentrations affect the graft content, and the desired graft content with minimal degradation can be obtained by controlling these factors. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 1693–1702, 1999 相似文献
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Synthesis and Characterization of CPE-g-GMA Graft Copolymers Obtained by Suspension Copolymerization
Graft of glycidyl methacrylate (GMA) onto solid-state chlorinated polyethylene (CPE) has been performed by suspension copolymerization in a complex dispersion medium which was a compound with H2O, ethyl acetate (EA) and tert-butyl alcohol (TBA). Benzoyl peroxide (BPO) was used as the free radical initiator. The graft level (graft degree and graft efficiency) was calculated gravimetrically, and the graft copolymer was characterized by infrared (IR) spectroscopy, thermogravimetric analysis (TGA) and contact angle study. The effects of reaction conditions on graft level, including chemical parameters (the concentration of monomer, initiator, and interfacial agent) and processing parameters (reaction time and temperature), have been investigated in detail. The experimental results showed that GMA could be grafted onto the chain of CPE with comparative higher graft degree, which could reach 37% with graft efficiency above 80%. 相似文献
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《高分子科学杂志,A辑:纯化学与应用化学》2013,50(10):1247-1260
Novel ampholytic grafted polysaccharides were prepared by grafting the Zwitterionic monomer 2-(2-methacryloethyldimeth-ylammonio) ethanoate onto hydroxyethyl cellulose. Ethylenediamine tetraacetic acid was used in combination with ceric ammonium nitrate as the redox initiator. The effects of various factors such as initiator amount, monomer concentration, reaction temperature and time on the grafting were studied and the optimum reaction conditions to obtain maximum degree of grafting were found. The resulted graft copolymer was characterized by IR and thermal analyses. 相似文献