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首页> 外文期刊>Food Hydrocolloids >Associative and segregative interactions between gelatin and low-methoxy pectin: Part 2―co-gelation in the presence of Ca~(2+)
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Associative and segregative interactions between gelatin and low-methoxy pectin: Part 2―co-gelation in the presence of Ca~(2+)

机译:明胶与低甲氧基果胶之间的缔合和偏析相互作用:第2部分– Ca〜(2+)存在下的共凝胶化

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摘要

The effect of segregative interactions with gelatin (type B; pI = 4.9; 0―10 wt%) on the networks formed by low-methoxy pectin on cooling in the presence of stoichiometric Ca~(2+) at pH 3.9 has been investigated by rheological measurements under low-amplitude oscillatory shear. Samples were prepared and loaded at 85℃, cooled (1℃/min) to 5℃, held for 100 min, and re-heated (1℃/min) to 85℃, with measurement of storage and loss moduli (G′ and G″) at 10 rad s~(-1) and 2% strain. The final values of G′ at 5℃ for mixtures prepared at the same pH without Ca~(2+) were virtually identical to those observed for the same concentrations (0.5―10.0 wt%) of gelatin alone, consistent with the conclusion from the preceding paper that electrostatic (associative) interactions between the two polymers become significant only at pH values below 3.9. Increases in moduli on cooling in the presence of Ca~(2+) occurred in two discrete steps, the first coincident with gelation of calcium pectinate alone and the second with gelation of gelatin. Both processes were fully reversible on heating, but displaced to higher temperature (by ~ 10℃), as was also observed for the individual components. The magnitude of the changes occurring over the temperature range of the gelatin sol―gel and gel―sol transitions demonstrates that the gelatin component forms a continuous network; survival of gel structure after completion of gelatin melting shows that the calcium pectinate network is also continuous (i.e. that the co-gel is bicontinuous). On progressive incorporation of NaCl (to induce phase separation before, or during, pectin gelation) the second melting process, coincident with loss of calcium pectinate gel structure, was progressively abolished, indicating conversion to a gelatin-continuous network with dispersed particles of calcium pectinate. These qualitative conclusions are supported by quantitative analyses reported in the following paper.
机译:研究了与明胶(B型; pI = 4.9; 0-10 wt%)的分离相互作用对低甲氧基果胶在pH 3.9的化学计量Ca〜(2+)存在下冷却形成的网络的影响。低振幅振荡剪切下的流变学测量。制备样品并在85℃下加载,以1℃/ min的速度冷却至5℃,保持100分钟,再以1℃/ min的温度加热至85℃,测量存储模量和损耗模量(G'和G'')在10 rad s〜(-1)和2%应变下。在相同pH下不含Ca〜(2+)的混合物中,在5℃下G'的最终值实际上与仅在相同浓度(0.5〜10.0 wt%)的明胶中观察到的值相同,这与从中得出的结论一致。先前的论文表明,只有当pH值低于3.9时,两种聚合物之间的静电(缔合)相互作用才变得显着。在存在Ca〜(2+)的情况下,冷却时模量的增加发生在两个离散的步骤中,第一个与果胶酸钙单独凝胶化同时发生,第二个与明胶凝胶化同时发生。这两个过程在加热时都是完全可逆的,但是转移到更高的温度(约10℃),对于单个组件也可以观察到。在明胶溶胶-凝胶和凝胶-溶胶转变温度范围内发生的变化幅度表明,明胶组分形成了连续的网络。明胶熔化完成后凝胶结构的存活率表明果胶酸钙网络也是连续的(即,共凝胶是双连续的)。随着NaCl的逐步掺入(在果胶凝胶化之前或之中引起相分离),第二次熔化过程(与果胶钙凝胶结构的丧失相伴而生)被逐步废除,表明转化为具有果胶钙分散颗粒的明胶连续网络。这些定性结论得到以下论文报道的定量分析的支持。

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