首页> 外文期刊>African Journal of Pure and Applied Chemistry >Effect of acid hydrolysis on the physicochemical properties of cola starch
【24h】

Effect of acid hydrolysis on the physicochemical properties of cola starch

机译:酸水解对可乐淀粉理化性质的影响

获取原文
           

摘要

Cola starch fromCola nitida (rubra)was isolated using 1% (w/v) sodium metabisulphite solution and was treated with 0.1 and 0.2 M HCl solution differently at 80 and 100°C, pH (6 to 7.9) and reaction time (30 min to 3 h). The physicochemical and functional properties of the hydrolyzed starch were studied. The hydrolysis reaction presented important changes in the pasting, thermal transition and morphology of the native starch. Reaction time, temperature and concentration of the acid were observed to influence the reactions. The acid modified starch has the following properties; swelling 6.13 to 7.21% solubility 14.83 to 16.65% and amylose content 17.28 to 21.69%, while the corresponding values for the native cola starch were swelling 8.85%, solubility 7.48% and amylose 24.76%. The rapid visco analysis (RVA) of the acid modified starch demonstrated low peak viscosity ranging from 52.71 to 197.22 as against 314.42 reported for the native starch. Breakdown viscosity and the setback values also exhibited the same decreasing trend; 30.24 to 73.17 and 10.18 to 34.91 respectively, as against that of native cola starch that has a breakdown and setback viscosity of 179.25 and 74.42 respectively. The observed trends are consistent with other modified starches that have found useful applications in pharmaceutical, food and confectionary industries.
机译:用1%(w / v)偏亚硫酸氢钠溶液分离可乐尼的可乐淀粉,并分别在80和100°C,pH(6至7.9)和反应时间(30分钟)下分别用0.1和0.2 M HCl溶液处理至3小时)。研究了水解淀粉的理化性质和功能特性。水解反应在天然淀粉的糊化,热转变和形态方面呈现出重要的变化。观察到反应时间,酸的温度和浓度影响反应。酸改性淀粉具有以下性质;溶胀6.13至7.21%,溶解度14.83至16.65%,直链淀粉含量17.28至21.69%,而天然可乐淀粉的相应值溶胀8.85%,溶解度7.48%和直链淀粉24.76%。酸改性淀粉的快速粘度分析(RVA)显示出低峰值粘度,范围为52.71至197.22,而天然淀粉为314.42。击穿粘度和挫折值也表现出相同的下降趋势;分别为30.24至73.17和10.18至34.91,而天然可乐淀粉的击穿和挫折粘度分别为179.25和74.42。观察到的趋势与已发现在制药,食品和糖果行业有用的其他改性淀粉相一致。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号