Kometani Noritsugu, Tanabe Masahiro, Su Lei, Yang Kun, Nishinari Katsuyoshi
‡The High Pressure Research Center of Science and Technology, Zhengzhou University of Light Industry, Zhengzhou 450002, China.
§Glyn O. Phillips Hydrocolloids Research Centre, School of Food and Pharmaceutical Engineering, Faculty of Light Industry, Hubei University of Technology, Wuchang, Wuhan 430068, China.
J Phys Chem B. 2015 Jun 4;119(22):6878-83. doi: 10.1021/acs.jpcb.5b03632. Epub 2015 May 27.
Thermoreversible sol-gel transitions of agarose and methylcellulose (MC) aqueous solutions on isobaric cooling or heating under high pressure up to 400 MPa have been investigated by in situ observations of optical transmittance and falling-ball experiments. For agarose, which undergoes the gelation on cooling, the application of pressure caused a gradual rise in the cloud-point temperature over the whole pressure range examined, which is almost consistent with the pressure dependence of gelling temperature estimated by falling-ball experiments, suggesting that agarose gel is stabilized by compression and that the gelation occurs nearly in parallel with phase separation under ambient and high-pressure conditions. For MC, which undergoes the gelation on heating, the cloud-point temperature showed a slight rise with an initial elevation of pressure up to ∼150 MPa, whereas it showed a marked depression above 200 MPa. In contrast, the gelling temperature of MC, which is nearly identical to the cloud-point temperature at ambient pressure, showed a monotonous rise with increasing pressure up to 350 MPa, which means that MC undergoes phase separation prior to gelation on heating under high pressure above 200 MPa. Similar results were obtained for the melting process of MC gel on cooling. The unique behavior of the sol-gel transition of MC under high pressure has been interpreted in terms of the destruction of hydrophobic hydration by compression.
通过对光透射率的原位观察和落球实验,研究了琼脂糖和甲基纤维素(MC)水溶液在高达400 MPa的高压下等压冷却或加热时的热可逆溶胶-凝胶转变。对于冷却时发生凝胶化的琼脂糖,在整个测试压力范围内,施加压力导致浊点温度逐渐升高,这与通过落球实验估计的凝胶化温度的压力依赖性几乎一致,表明琼脂糖凝胶通过压缩得以稳定,并且在常压和高压条件下凝胶化几乎与相分离同时发生。对于加热时发生凝胶化的MC,浊点温度在压力初始升高至约150 MPa时略有上升,而在压力高于200 MPa时则显著下降。相比之下,但在常压下与浊点温度几乎相同的MC凝胶化温度,在压力增加至350 MPa时单调上升,这意味着MC在高于200 MPa的高压下加热时,在凝胶化之前先发生相分离。在冷却时MC凝胶的熔化过程也得到了类似的结果。MC在高压下溶胶-凝胶转变的独特行为已根据压缩对疏水水合作用的破坏来解释。