Fluctuations, Order, and Disorder in Short Diblock Copolymers

被引:92
|
作者
Lee, Sangwoo [1 ]
Gillard, Timothy M. [1 ]
Bates, Frank S. [1 ]
机构
[1] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
基金
美国国家科学基金会;
关键词
block copolymers; fluctuations; phase behavior; MICROPHASE SEPARATION TRANSITION; BLOCK-COPOLYMERS; STRONG-SEGREGATION; CHAIN DIMENSIONS; PHASE-BEHAVIOR; MICELLE REGIME; FRANK-KASPER; MELTS; POLYMERS; POLYDISPERSITY;
D O I
10.1002/aic.14023
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The phase behavior for a series of poly(1,4-isoprene-b-DL-lactide) diblock copolymers characterized by a relatively large Flory-Huggins segment-segment interaction parameter () and low degrees of polymerization (N) over a range of compositions was reported. Ordered-state morphologies were deduced from small-angle x-ray scattering (SAXS) measurements, and (T) was determined from order-disorder transition temperatures (T-ODT's) associated with the compositionally symmetric specimens and assuming the mean-field theory, that is, (N)(ODT)=10.5. The ODT was determined by differential scanning calorimetry, SAXS, and dynamic mechanical spectroscopy, and shown to be weakly first-order, with latent heats of transition that vary strongly with composition. We interpret this behavior in terms of the mean and Gauss interfacial curvature of the ordered-state morphologies and with respect to composition fluctuations in the disordered state. These results offer a fresh strategy for investigating weakly first-order phase transitions within the Brazovskii universality class. (c) 2013 American Institute of Chemical Engineers AIChE J, 59: 3502-3513, 2013
引用
收藏
页码:3502 / 3513
页数:12
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