Cho Junhan
Department of Polymer Science & Engineering and Center for Photofunctional Energy Materials, Dankook University, 126 Jukjeon-dong, Suji-gu, Yongin-si, Gyeonggi-do 448-701, Korea.
ACS Macro Lett. 2013 Jun 18;2(6):544-549. doi: 10.1021/mz400111x. Epub 2013 Jun 5.
We investigate theoretically the response of interfacial tension γ for compressible polymer blends to thermodynamic variables. Helfand's self-consistent field theory is first extended to be combined with an off-lattice equation-of-state model to describe compressibility. Typical incompatible blends reveal that the effects of temperature and pressure (-) on γ are superposed into a single curve by a dimensionless pressure variable through the superposition in Flory-Huggins χ and density. In the case of polymer blends with strong compressibility difference, γ shows an anomaly upon pressurization with no - superposition, even though χ still follows the superposition.
我们从理论上研究了可压缩聚合物共混物的界面张力γ对热力学变量的响应。首先将赫尔芬德自洽场理论进行扩展,使其与非晶格状态方程模型相结合,以描述可压缩性。典型的不相容共混物表明,温度和压力(-)对γ的影响通过弗洛里-哈金斯χ和密度的叠加,由一个无量纲压力变量叠加到一条单一曲线上。对于具有强可压缩性差异的聚合物共混物,即使χ仍遵循叠加规律,但γ在加压时会出现异常,不存在叠加现象。