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Synthesis and Characterization of Cross-linked Carboxymethyl Potato Starch Ether Gels

机译:交联羧甲基马铃薯淀粉醚凝胶的合成与表征

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摘要

Hydrogels were synthesized by cross-linking of potato starch (PS) with dichloroacetic acid (DCA) in the presence of monochloroacetic acid (MCA) to form etherified carboxy-methyl starch (CMS) gels, to be used for ultrasonic medical examinations. By ether-ification cross-linked CMS-hydrogels can be produced, that are stable in contrast to the in the long-term unstable esterified gels, that were presented in the last paper. The rheological benchmarks for the CMS-hydrogels were set in comparison with synthetic ultrasonic gels. Gels with potato starch contents in the reaction batch ranging from 12.5% to 20% showed the best compliance with the benchmark parameters. The DS values of these CMS-hydrogels vary from 0.42 to 0.49, increasing with decreasing amount of starch in the reaction mixture. The free swelling capacities (FSC) vary between 77 g/g for the 12.5% PS-gel and 34 g/g for 20% PS-gel, the turbidities of the samples being in the range from 14.5 NTU (Nephelometric Turbidity Units) (12.5% PS) up to20.5 NTU (20% PS). The variation of the PS fraction in the reaction mixture showed that with an increased amount of PS in the reaction batch the number of cross-links of the CMS-gels increases, too. At a higher number of cross-links the swelling capacity is reduced and the concentration needed to form stable hydrogels is greatly increased. Thus a hydrogel of a polymer concentration of 5 mass-% from a 12.5% PS batch was produced, that showed the best accordance with the rheological benchmark parameterssuch as gelatinization time, visco-elastic and pseudoplastic properties and long-term stability. The ultrasonic pictures taken with this CMS-gel were not different from those taken with the synthetic gels. This hydrogel was then subjected to long-term-stability measurements performed over one year and to rheological temperature cycle tests. The tests showed that the long-term stability of the gels is sufficient for their use as ultrasonic gel.
机译:在一氯乙酸(MCA)存在下,马铃薯淀粉(PS)与二氯乙酸(DCA)交联以形成醚化的羧甲基淀粉(CMS)凝胶,从而合成水凝胶,用于超声医学检查。通过醚化,可以生产交联的CMS-水凝胶,与上篇论文中提出的长期不稳定的酯化凝胶相反,它是稳定的。与合成超声凝胶相比,设定了CMS-水凝胶的流变基准。反应批中马铃薯淀粉含量为12.5%至20%的凝胶表现出最佳的基准参数依从性。这些CMS-水凝胶的DS值在0.42至0.49之间变化,随着反应混合物中淀粉量的减少而增加。对于12.5%PS-凝胶,自由溶胀能力(FSC)为77 g / g,对于20%PS-凝胶,自由溶胀能力为34 g / g,样品的浊度为14.5 NTU(比浊法浊度单位)( 12.5%PS)至20.5 NTU(20%PS)。反应混合物中PS组分的变化表明,随着反应批料中PS含量的增加,CMS凝胶的交联数也随之增加。随着交联数量的增加,溶胀能力降低,形成稳定水凝胶所需的浓度大大增加。因此,从12.5%的PS批料中生产出聚合物浓度为5质量%的水凝胶,其表现出与流变基准参数如糊化时间,粘弹性和假塑性特性以及长期稳定性最佳的一致性。用这种CMS-凝胶拍摄的超声图像与用合成凝胶拍摄的超声图像没有区别。然后对该水凝胶进行一年以上的长期稳定性测量并进行流变温度循环测试。测试表明,凝胶的长期稳定性足以用作超声凝胶。

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