...
首页> 外文期刊>Food Hydrocolloids >Molecular structures of gellan gum imaged with atomic force microscopy in relation to the rheological behavior in aqueous systems. 1. Gellan gum with various acyl contents in the presence and absence of potassium
【24h】

Molecular structures of gellan gum imaged with atomic force microscopy in relation to the rheological behavior in aqueous systems. 1. Gellan gum with various acyl contents in the presence and absence of potassium

机译:用原子力显微镜成像的结冷胶的分子结构与水性体系中的流变行为有关。 1.在有钾和无钾条件下,具有各种酰基含量的吉兰糖胶

获取原文
获取原文并翻译 | 示例
           

摘要

Four samples of gellan gum in sodium form, with equivalent average molar mass but with different acyl contents, were investigated using atomic force microscopy (AFM) and dynamic viscoelasticity measurements. The investigation was carried out at concentrations which form local molecular assemblies, including associations, networks, and gels. AFM showed that continuous network structures developed mainly through end-to-end type inter-helical associations rather than side-by-side type ones in the presence of potassium without significant increase in the vertical height on the image. Although end-to-end type inter-helical associations certainly occurred, continuous network structures did not develop in the absence of potassium. In the presence of the cation, the formation of continuous network structures could relate to the rheological thermal hysteresis between the sol-to-gel and the gel-to-sol transitions and to the dynamic storage modulus at 20 ℃ for gellan gum with lower acyl contents. During gelation, acyl groups increase the flexibility of the molecular bundles, inhibiting associations between the backbones when the added potassium minimizes the electrostatic repulsion. Also, acyl groups lower the charge density of the molecular bundles, which would promote associations in the absence of the cation or the stabilization of the double helix (especially via glycerate groups). This would increase the elasticity of the gelled system in the absence of the cation. Our results point to the fibrous model of gelation rather than the conventional model that assumes distinct junction zones with disordered flexible polymer chains connecting adjacent junction zones.
机译:使用原子力显微镜(AFM)和动态粘弹性测量方法研究了四种形式为钠形式的吉兰糖胶样品,这些样品具有相等的平均摩尔质量,但酰基含量不同。研究是在形成局部分子组装体(包括缔合体,网络和凝胶)的浓度下进行的。原子力显微镜显示,连续的网络结构主要通过端到端类型的螺旋间缔合而不是在钾存在下并排类型而形成,而图像的垂直高度没有明显增加。尽管确实发生了端到端类型的螺旋间缔合,但是在缺少钾的情况下并没有形成连续的网络结构。在阳离子存在下,连续网络结构的形成可能与溶胶-凝胶和凝胶-溶胶转变之间的流变热滞后以及低酰基结冷胶在20℃时的动态储能模量有关。内容。在胶凝过程中,酰基会增加分子束的柔韧性,并在添加的钾使静电排斥最小时抑制主链之间的缔合。同样,酰基降低了分子束的电荷密度,这将在不存在阳离子或双螺旋稳定化的情况下促进缔合(特别是通过甘油酸酯基)。在不存在阳离子的情况下,这将增加胶凝体系的弹性。我们的结果指向了凝胶化的纤维模型,而不是传统的模型,该模型假定不同的连接区域具有无序的柔性聚合物链连接相邻的连接区域。

著录项

相似文献

  • 外文文献
  • 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