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微波法合成淀粉接枝丙烯酸盐类高吸水性树脂的研究 总被引:18,自引:0,他引:18
以N,N′-亚甲基双丙烯酰胺为交联剂、过硫酸铵为引发剂、在微波辐照下对淀粉接枝丙烯酸盐共聚进行了系统的研究,确定了最佳的反应条件,合成了粉末状的高吸水性树脂。并用FTIR和固体NMR等方法探讨了淀粉一丙烯酸盐接枝共聚物的结构特征。实验结果表明,利用微波技术合成淀粉一丙烯酸盐接枝共聚物可实现一次合成、干燥,简化合成工艺。淀粉与丙烯酸盐质量比为40/100左右时产物的接枝率最大,且吸水速率明显高于化学法合成的高吸水树脂。 相似文献
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聚氯乙烯-g-聚甲基丙烯酸-2-羟乙酯共聚物的合成和表征 总被引:4,自引:0,他引:4
聚氯乙烯 (PVC)是常用医用高分子材料之一 ,可以制作储血袋、导液管、人工尿道等 .PVC亲水性差 ,影响其生物相容性 .采用亲水性单体与PVC接枝共聚是提高PVC亲水性的重要方法[1] .Krishnan等[2 ] 对Co60 辐照下PVC接枝N 乙烯基吡咯烷酮进行了研究 .Singh等[3~ 5] 采用辐照引发甲基丙烯酸在PVC薄膜的接枝反应 ,对接枝动力学、接枝后薄膜表面形态、溶胀和抗凝血性等进行了研究 .Goldberg等[6] 采用辐照引发甲基丙烯酸2 羟乙酯 (HEMA)在PVC薄膜上的接枝 .Lee等[7]采用溶液接枝共聚制备了… 相似文献
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在四氢呋喃、环己酮等溶液中实现了聚氯乙烯(PVC)与聚苯乙烯(PS)的Friedel-Crafts接枝反应,考察了加热方式、反应温度、催化剂种类、催化剂用量对接枝反应的影响,通过FTIR表征了PVC-g-PS接枝物的结构,探讨了反应的机理和特点.研究发现,油浴加热和微波辐照都能使PVC和PS发生接枝反应,但微波辐照效果更好,油浴加热,接枝率仅0.27%,而微波辐照接枝率高达23%;油浴加热时产物少且多为间位,微波辐照时产物多且多为对位和邻位.无水AlCl3、无水FeCl3、无水SnCl4皆对PVC与PS之间的Friedel-Crafts反应具有催化活性,其中无水AlCl3的催化活性最高,其最佳用量为质量分数3%,此时,接枝率达到29%.当无水AlCl3过高时,PVC降解,产生双键,接枝率下降.表明微波辐照是实现PVC与PS之间Friedel-Crafts接枝反应的有效途径. 相似文献
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采用紫外光引发接枝表面改性的方法,以芴酮(FL)为引发剂,在低密度聚乙烯(LDPE)薄膜表面上接枝丙烯酸(AA)、甲基丙烯酸(MAA)、丙烯酸甲酯(MA)、甲基丙烯酸甲酯(MMA)、丙烯酰胺(AM)等单体,以赋予薄膜表面新的化学性质.考察了引发剂浓度、紫外光的辐照时间、辐照强度、单体种类对LDPE薄膜接枝程度的影响.结果表明,在一定范围内,增加芴酮浓度,可以提高单体的接枝率,但当芴酮浓度达到5%时,接枝率反而下降.延长辐照时间至4 min和提高紫外光的辐照强度达100 W/m2,均有利于接枝反应的进行.不同单体在LDPE膜上的接枝能力与单体的活性、单体与基材的相容性等因素有关.接枝后,LDPE与水的接触角下降程度不仅与单体在膜上的接枝量有关,还与接枝单体的亲水性能密切相关. 相似文献
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丙烯酸β-羟丙酯与聚氯乙烯膜的紫外光接枝改性 总被引:4,自引:0,他引:4
采用液相接枝方法 ,在紫外线辐照下 ,合成了一系列丙烯酸 β-羟丙酯 (β -HPAT) /聚氯乙烯接枝膜。讨论了引发剂浓度、单体浓度、光照时间、光照强度对接枝率的影响。结果表明 ,引发剂浓度为 6 .5 1× 10 -3 mol/L ,单体浓度 2 .0mol/L ,光照时间为 2 .0h ,且光照强度越强时 ,接枝率最大。接枝膜的结构特征通过FT -IR光谱进行了确证 ,最后 ,对接枝膜进行TGA分析 ,结果表明聚氯乙烯经过表面改性后 ,表面极性增大 ,热稳定性大大提高。 相似文献
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采用填加SiO_2增强的甲基乙烯基硅橡胶混炼压片。通过~(60)Co-γ射线引发辐射硫化,利用共辐照方法,将N-乙烯基吡咯烷酮接枝到该硅橡胶上,制备了高纯度医用水凝胶。本文较系统地研究了接枝单体浓度、辐照剂量率、剂量、温度和接枝试片厚度等因素对接枝共聚反应的影响。建立了接枝速率与单体浓度、剂量率之间的动力学关系式:R_g=k[M]~(4/5)D~(1/2)。讨论了反应机制和接枝区域。 相似文献
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Graft copolymerization of ethylmethacrylate (EMA) onto soy protein concentrate (SPC) was carried-out using ascorbic acid/potassium persulphate as redox initiator under microwave radiations. Different reaction parameters like reaction time, solvent amount, initiator ratio, pH and monomer concentration were optimized to get maximum graft yield (78.8%). The graft copolymer formed was characterized by FTIR, XRD, SEM, TGA, DTA and DTG techniques. Graft copolymer showed higher moisture resistance along with increased chemical and thermal stability. TGA, DTA and DTG studies could reveal the distinctive features of graft copolymerization of EMA onto S-S linkages of soy protein concentrate under the influence of microwave irradiations in addition to grafting at peptide linkages, which were further supported by FT-IR studies. 相似文献
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SBS与甲基丙烯酸丁酯本体接枝反应的研究 总被引:1,自引:0,他引:1
本文研究了以过氧化苯甲酰(BPO)为引发剂,甲基丙烯酸丁酯(BMA)既作溶剂又作为单体与苯乙烯-丁二烯嵌段共聚物(SBS)进行接枝共聚反应。用红外光谱、核磁共振谱及透射电镜表征了接枝共聚物(SBS-g-BMA)的组成及结构,讨论了时间、温度及SBS和BPO的用量对接枝的影响。 相似文献
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A super‐absorbent polymer was prepared by grafting copolymerization of acrylic acid onto Artemisia seed gum, using microwave irradiation and ammonium persulfate as an initiator. The effect of various preparation conditions on its water absorbency, such as the ratio of acrylic acid to Artemisia seed gum, degree of acrylic acid neutralization, amount of initiator and microwave irradiation time, was investigated by orthogonal tests. The optimal reaction conditions were 3 min (irradiation time), 70% neutralization degree of acrylic acid and 2% initiator on the basis of the mass of acrylic acid used. When the mass ratio of acrylic acid to Artemisia seed gum is 5:0.5, the product has a water absorbency close to 400 times at room temperature in distilled water, this indicated that is has a high water absorbency. The structure of the graft copolymer was confirmed by Fourier transform infrared spectrometer (FT‐IR) and thermogravimetric analysis (TGA). Further more, this microwave irradiation processing method to prepare water absorbent materials has no industrial cast off produced, that is to say, this method is environmentally friendly. 相似文献
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Nanthaporn Pukkate Yoshimasa Yamamoto Seiichi Kawahara 《Colloid and polymer science》2008,286(4):411-416
High conversion and high grafting efficiency attained by graft copolymerization of styrene onto deproteinized natural rubber
(DPNR) was investigated with respect to the molecular weight of grafted polystyrene. The graft copolymerization was performed
with tert-butyl hydroperoxide/tetraethylenepentamine as an initiator after deproteinization of natural rubber with urea. Grafted polystyrene
was isolated from the resulting graft copolymer by ozonolysis reaction. After the ozonolysis of the graft copolymer of DPNR
and polystyrene (DPNR-g-PS), the molecular weight of grafted polystyrene was determined by size exclusion chromatography. Effects of initiator and
monomer concentrations were investigated with respect to the molecular weight of the grafted polystyrene, which was found
to depend on not only the number of active site generated on the rubber particle but also the feed of styrene. Deactivation
and chain transfer of the active sites were attributed to effective amount of styrene used for the graft copolymerization. 相似文献
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壳多糖与丙烯酸丁酯的乳液接枝共聚研究 总被引:10,自引:0,他引:10
以十二烷基苯磺酸钠为乳化剂,过硫酸钾-亚硫酸氢钠为引发剂,研究了壳多糖与丙烯酸丁醋的乳液共聚合,结果表明当[K2S2O8]=[NaHSO3]=2.57×10-3mol·1-1,[BA]=0.68mol.1-1,[Chitosan]=19.2g·l-1,在70℃下反应5小时,共聚反应的接技率和接枝效率均较高.用红外光谱,差热分析,X射线衍射,扫描电镜对接技共聚物进行了表征,此外测试了共聚物胶乳成膜的机械性能,表明用丙烯酸丁酯对壳多糖进行接枝改性,可提高壳多糖的韧性,扩大其应用范围. 相似文献
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二过碘酸合铜(Ⅲ)钾引发丙烯腈在聚丙烯酰胺上接枝共聚合反应的研究 总被引:1,自引:0,他引:1
本文以二过碘酸合铜(Ⅲ)钾为氧化剂,聚丙烯酰胺(PAAM)自身为还原剂组成的氧化还原引发体系,在PAAM上引发丙烯腈接枝共聚合反应,获得了高接枝效率和高接枝百分比的产物,由红外光谱、扫描电镜及X射线衍射分析对接枝反应进行了表征,测定了各种条件对接枝参数的影响,并对引发机理进行了探讨。 相似文献
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Abstract The photoinduced graft copolymerization of methyl methacrylate onto cellulose was studied using N-bromosuccinimide as the photoinitiator. The formation of graft copolymer increases with an increasing amount of cellulose. The graft copolymerization increases with increasing initiator concentration up to 1,25 × 10?2 M and thereafter it decreases. The percentage of graft increases with increasing monomer concentration up to 46.9 × 10?2 M and thereafter it decreases. The percentage graft-on increases with increasing temperature. The overall activation energy was computed to be 8.40 kcal/mol. The percentage graft was investigated using different water-miscible organic solvents. The graft copolymerization was also investigated using differently modified cellulose. A possible mechanism for the photo-graft copolymerization onto cellulose is suggested. 相似文献