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Processing and formulation effects on rheological behavior of barley β-glucan aqueous dispersions

机译:大麦β-葡聚糖水分散体的加工和配方对流变行为的影响

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A freeze-thaw cycling process applied to barley β-glucan aqueous dispersions resulted in network structure development, which remained intact after thawing in both acidic and neutral conditions. The effects of freeze-thaw cycling were milder in the presence of sucrose where β-glucans were less prone to cryogel formation, giving weaker cryostructurates. The effect of three operating factors (β-glucan content, sucrose content and salt content) and their interactions on viscosity at shear rates of 10, 50 and 125 s~(-1) was studied using response surface methodology. Significant positive linear effects were identified for all the factors on the first two models, while salt was not significant for the response at 125 s~(-1). The β-glucan also exhibited significant negative quadratic effects for all three responses. Significant negative interactions were observed between β-glucan and sucrose, and β-glucan and salt for the viscosity at 10 and 50 s~(-1), while for the viscosity at 125 s~(-1), only the interaction between β-glucan and sucrose was significant. Response surface methodology and a second order regression model were used for the study of three factors (pH, temperature and time) influencing the viscosity of β-glucan dispersions of a low and a high molecular weight sample, following acid hydrolysis. Significant linear effects on viscosity of the low and high molecular weight samples were obtained for all the factors. A significant positive interaction effect was observed between pH and time for the viscosity of the lower molecular weight sample, while time exhibited a significant negative quadratic effect for the response of the high molecular weight sample. Acid hydrolysis had a stronger impact on viscosity reduction of the high molecular weight sample.
机译:应用于大麦β-葡聚糖水分散体的冻融循环过程导致网络结构发展,在酸性和中性条件下融化后仍保持完整。在蔗糖存在下,β-葡聚糖不易形成冰冻凝胶,而冻融循环的影响则较弱,从而使冰冻结构较弱。利用响应面法研究了三种操作因素(β-葡聚糖含量,蔗糖含量和盐含量)及其相互作用对剪切速率分别为10、50和125 s〜(-1)时的粘度的影响。在前两个模型中,所有因素均具有显着的线性正效应,而盐对125 s〜(-1)的响应不显着。对于所有三个响应,β-葡聚糖还表现出显着的负二次效应。在10和50 s〜(-1)的粘度下,β-葡聚糖和蔗糖以及β-葡聚糖和盐之间观察到显着的负相互作用,而在125 s〜(-1)的粘度下,只有β之间的相互作用-葡聚糖和蔗糖是显着的。响应表面方法和二阶回归模型用于研究酸水解后影响低分子量和高分子量样品的β-葡聚糖分散体粘度的三个因素(pH,温度和时间)。对于所有因素,均获得了对低分子量和高分子量样品粘度的显着线性影响。对于较低分子量样品的粘度,在pH和时间之间观察到显着的正相互作用效应,而对于高分子量样品的响应,时间表现出显着的负二次效应。酸水解对高分子量样品的粘度降低具有更强的影响。

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