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CAN - KPS体系引发淀粉接枝共聚为絮凝剂的工艺研究 总被引:2,自引:0,他引:2
为克服引发剂铈盐较昂贵,工业应用难的缺点,实验采用CAN-KPS复合引发体系引发丙烯腈接枝改性淀粉,采用接枝率和接枝效率作为评价接枝效果的指标,详细研究了接枝工艺及其引发剂浓度、丙烯腈单体的用量和接枝温度对接枝率和接枝效率的影响,结果表明:接枝率达130%以上,接枝效率达90%以上,可较好地代替铈盐引发剂。接枝后对接枝淀粉的结构分析表明:淀粉大分子上已接枝上丙烯腈单体;接枝反应不仅发生在淀粉的无定形区也发生在结晶区,且接枝后接枝淀粉的结晶度有所提高。 相似文献
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Allylurea (AU) was used as a reactive additive with poor aptitude to homopolymerization for obtaining grafted plasticized starch films with stabilized physical properties. Potato starch was mixed with AU (30–50 parts per hundred/pph) in a mixer operating at 125°C. Upon storage in well‐defined hygrothermal conditions, the resulting thermoplastic material shows strong plasticizer migration revealed by AU crystals blooming at the samples surface and exhibits strong opacity assigned to phase separation of the organic additive inside the material. Freshly prepared thermoplastic films of appropriate thickness were exposed to a 175‐kV electron beam (EB) radiation for inducing covalent grafting of AU by a free radical process. FTIR monitoring of the resulting chemical changes in thin films of AU–starch blends indicates unambiguously the transformation of AU allylic bond. High irradiation doses are required for achieving complete conversion of AU in the blend. However, no detectable AU migration was observed for intermediate AU conversion, probably as a consequence of higher plasticizer solubility in the grafted polysaccharide. Examination of the viscoelastic properties by dynamic mechanical thermal analysis shows that artificial aging by placing the films alternatively in high and low relative humidity (RH) atmosphere does not significantly alter the thermomechanical spectrum of the material reconditioned in a cell at 58% RH. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 73: 409–417, 1999 相似文献
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Potato starch phosphate (PSP) particles were synthesized via an esterification process of potato starch with a mixture of various concentrations of phosphoric acid and urea. The electrorheological (ER) characteristics of the synthesized PSP particles, suspended in a silicone oil, were examined. The PSP granule‐based ER fluid exhibited typical ER behavior, possessing a nonvanishing yield stress under an applied electric field. Enhanced polarization and higher yield stresses were observed as the content of phosphate groups in the starch increases. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1770–1773, 2004 相似文献
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氧化还原引发下的淀粉、丙烯酸反相乳液聚合 总被引:3,自引:0,他引:3
以环己烷为连续相,Span20为乳化剂,采用氧化还原引发体系,通过反相乳液聚合技术,合成淀粉、丙烯酸接枝共聚物。并用红外光谱对共聚物进行了表征。研究结果表明:采用氧化还原引发剂可使聚合反应低温快速进行,在过硫酸钾为3.1mmol/L,亚硫酸氢钠为3.1mmol/L,单体丙烯酸浓度为2.6mol/L,反应温度为30℃,反应时间为3h,乳化剂浓度为5%时,单体转化率为92.6%、淀粉接枝率为43.2%、淀粉接枝效率56.4%。 相似文献
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在室温下,以马铃薯淀粉为原料,双氧水为氧化剂,制备出了马铃薯淀粉粘合剂.探讨了氧化剂用量、催化剂用量、糊化剂用量、氧化时间、糊化时间、粉水比、络合剂用量对粘合剂性能的影响,以粘度和初粘力为评价指标,通过L18(37)正交试验确定制备淀粉粘合剂的最佳条件为:m(水)∶m(马铃薯淀粉)=5∶1,双氧水1.3 mL,硫酸亚铁0.2 g,NaOH为3.0 g,氧化时间90 min,糊化时间30 min,硼砂0.3 g.并以添加聚乙烯醇进行接枝改性,提高其干燥时间和初粘力,实验得到添加量为5%时效果最好. 相似文献
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A structure‐exact starch‐based xanthate agent was prepared and used as chain transfer agent to mediate RAFT polymerization of vinyl acetate, which offered a convenient way to well control the structure and composition of starch‐g‐poly(vinyl acetate). The structures of the intermediate and the polymer were verified with FTIR and 1H‐NMR. Gel permeation chromatography measurement results indicated that the polymerization was performed as expected. It was found that the relationship between number average molecular weight and monomer conversion was linear. The polydispersity index of grafted side‐chain ranged from 1.19 to 1.53 and most of them were around 1.2. There was one more degradation stage appeared on the thermogravimetric analysis profile of starch‐g‐poly(vinyl acetate) than that of starch. TEM observation exhibited that the product was able to self‐assemble into micelles in aqueous solution, which suggested the copolymer was amphiphilic. Both the thermal and amphiphilic properties demonstrated the starch‐g‐poly(vinyl acetate) was successfully synthesized as well. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012 相似文献
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聚丙烯纤维接枝苯乙烯的研究 总被引:1,自引:0,他引:1
采用化学接枝法以苯乙烯(St)为接枝单体、过氧化苯甲酰(BPO)为引发剂,1,2-二乙烯苯(DVB)为交联剂、甲醇和正辛醇为溶剂,对聚丙烯(PP)纤维进行接枝改性。研究了原料配比和反应条件对其接枝的影响。结果表明,PP纤维上接枝St,适宜的原料配比和操作条件为:St质量与PP体积比(St/PP)为4,BPO质量与St体积比(BPO/St)为0.025,DVB与St体积比(DVB/St)为0.025,溶剂与St体积比为5,浸渍24~30h,在85℃恒温水浴中反应6~8h。在较佳条件下可得到导入率为110%-160%的接枝纤维。 相似文献
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IC反应器处理马铃薯淀粉生产废水的试验研究 总被引:4,自引:1,他引:4
试验采用超滤-IC反应器-MBR工艺处理马铃薯淀粉生产废水,重点研究了IC反应器处理马铃薯淀粉废水的工艺参数。结果表明,在常温下,当进水COD的质量浓度为6000~9000mg/L、HRT为5h、容积负荷为23.62kg[COD]/(m3·d)时,IC反应器对COD的去除率为91.43%。采用该工艺处理马铃薯淀粉生产废水完全可以达到废水回用的目的。 相似文献
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Preparation and characterization of grafting styrene onto LLDPE by cyclohexane compatibilization in suspension polymerization 下载免费PDF全文
A novel method of grafting styrene onto linear low‐density polyethylene (LLDPE) by suspension polymerization was systematically evaluated. Cyclohexane as a compatibilizer was introduced to swell and activate the surface of LLDPE molecular chain for amplifying the contact point of styrene monomer with LLDPE. A series of copolymer of grafting polystyrene (PS) onto LLDPE, known as LLDPE‐g‐PS, were prepared with different ratios of cyclohexane/styrene monomer and various LLDPE dosages. FTIR and 1H NMR techniques both confirmed successful PS grafting onto the LLDPE chains. In addition, SEM images of LLDPE‐g‐PS particles showed that the cross‐section morphology becomes smooth and dense with suitable cyclohexane dosages, indicating a better compatibility between LLDPE and PS. The highest grafting efficiency was 28.4% at 10 mL/g cyclohexane and styrene monomer when 8% LLDPE was added. In these conditions, the LLDPE‐g‐PS elongation at break increased by about 30 times compared with PS. Moreover, thermal gravimetric analysis (TGA) demonstrated that LLDPE‐g‐PS possesses much higher thermal stability than pure PS. Therefore, the optimal amount of cyclohexane as compatibilizer could increase the grafting efficiency and improve the toughness of PS. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41671. 相似文献
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淀粉的羧甲基化研究 总被引:12,自引:0,他引:12
研究了不同原料配比 (淀粉、CH2 ClCOOH及NaOH的用量 )、反应介质以及反应时间等对淀粉羧甲基化反应的影响。结果表明 ,在其它条件不变时 ,( 1)当NaOH用量不大时 ,随着NaOH用量的增加 ,取代度 (DS)和CH2 ClCOOH的反应效率(RE)亦增加 ,当NaOH与CH2 ClCOOH的摩尔比为 2 .5∶1时 ,达到最大值 ,其后随着NaOH的增加 ,DS和RE急剧下降 ;( 2 )随着CH2 ClCOOH用量的增加 ,DS和RE增加 ,其中DS在CH2 ClCOOH与淀粉中葡萄糖基的摩尔比增大到 1∶1时达到最大值 ,而RE在CH2 ClCOOH与淀粉中葡萄糖基的摩尔比为 0 .75∶1时达到最高 ;异丙醇作为反应介质优于乙醇 ;在本实验的时间范围内 ,DS随着反应时间的增长而增大 相似文献