Department of Range and Wildlife Management, Texas Tech University, Lubbock, Texas 79409.
Plant Physiol. 1981 Jan;67(1):64-7. doi: 10.1104/pp.67.1.64.
Water potential (Psiomega) values were determined for aqueous colloids of four molecular sizes of polyethylene glycol (PEG) using freezing-point depression and vapor-pressure deficit methods. A significant third-order interaction exists between the method used to determine Psiomega, PEG molecular size, and concentration. At low PEG concentrations, freezing-point depression measurements result in higher (less negative) values for Psiomega than do vapor-pressure deficit measurements. The reverse is true at high concentrations. PEG in water does not behave according to van't Hoff's law. Psiomega is related to molality for a given PEG but not linearly. Moreover, Psiomega varies with the molecular size of the PEG. It is suggested that the Psiomega of PEG in water may be controlled primarily by the matric forces of ethylene oxide subunits of the PEG polymer. The term matricum is proposed for PEG in soil-plant-water relation studies.
利用冰点降低和蒸汽压亏缺法测定了四种分子大小的聚乙二醇(PEG)水胶体的水势(Psiomega)值。用于测定 Psiomega 的方法、PEG 分子大小和浓度之间存在显著的三阶相互作用。在低 PEG 浓度下,冰点降低测量得到的 Psiomega 值比蒸汽压亏缺测量得到的 Psiomega 值更高(更负)。在高浓度下则相反。PEG 在水中的行为不符合范特霍夫定律。Psiomega 与给定 PEG 的克分子数有关,但不是线性关系。此外,Psiomega 随 PEG 分子大小而变化。因此,建议 PEG 在水中的 Psiomega 主要由 PEG 聚合物的环氧乙烷亚基的基质力控制。在土壤-植物-水关系研究中,提出了“基质”一词来表示 PEG。