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Influence of Pressure-assisted Freezing on the Structure, Hydration and Mechanical Properties of a Protein Gel

机译:压力辅助冷冻对蛋白质凝胶结构,水合和力学性能的影响

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摘要

Due to renewed interest in high pressure technology (2), the phase diagram of water under pressure (1) has been reexamined in view of potential food applications (4,8). Since water remains liquid until -22 deg C at a pressure of 207,5 MPa, pressure-shift freezing, pressure-assisted thawing and non frozen storage under pressure are all possible in the 0 to -22 deg C rang. For pressure-shift freezing, a biological sample is cooled under pressure to a temperature just above the melting temperature of ice at this pressure. Upon sudden pressure release, supercooling of water present in the sample enhances heterogeneous ice nucleation (12), inducing the formation of a large number of small stable ice nuclei. These give rise, after crystal growth, to a large number of small ice crystals, thus avoiding the damage to tissue and cell structures caused by large crystals with resulting drip and altered texture after thawing. Pressure-shift freezing may also lead to a uniform size distribution of ice crystals throughout the sample, since the initial supercooling is quasi-uniform throughout sample depth. To maintain these advantages, however, the latent heat of crystallization should be removed quickly, and this requires a low temperature or a stirred cooling medium and/or a small sample size. Low temperature frozen storage would be mandatory, to avoid ice recrystallization.
机译:由于对高压技术(2)的重新兴趣,考虑到潜在的食品应用(4,8),重新审视了压力(1)下的水相图。由于水保持液体直到-22℃,在207,5MPa的压力下,压力凝结,​​压力辅助解冻和在压力下的非冷冻储存在0至-22℃rang中。对于压力变化冷冻,将生物样品在压力下冷却至在该压力下冰熔温的温度。在突然的压力释放后,样品中存在的水的过冷增强了异质冰核(12),诱导大量小稳定冰核的形成。这些在晶体生长后产生了大量小冰晶,从而避免了由大晶体引起的组织和细胞结构的损害,并在解冻后产生滴水和改变的纹理。压力移冰也可能导致在整个样品中均匀尺寸分布,因为初始过冷在样品深度的准均匀。然而,为了保持这些优点,应快速去除结晶的潜热,并且这需要低温或搅拌的冷却介质和/或小样品尺寸。低温冷冻储存将是强制性的,以避免再重结晶。

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