CRITICAL-TEMPERATURE AND CONCENTRATION VERSUS MOLECULAR-WEIGHT IN POLYMER BLENDS - CONFORMATIONS, FLUCTUATIONS, AND THE GINZBURG CRITERION

被引:43
作者
HOLYST, R [1 ]
VILGIS, TA [1 ]
机构
[1] MAX PLANCK INST POLYMER RES, D-55021 MAINZ, GERMANY
关键词
D O I
10.1063/1.466031
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We use the field-theoretical methods to derive the self-consistent one-loop equations (Hartree approximation) for the location of the critical point in binary mixtures of polymers. The small parameter in the loop expansion is the inverse of the square root of the number of segments (monomers) in a polymer chain 1/ square-root N. Both the ideal chain conformation and fluctuation corrections to the Flory-Huggins mean field result are taken into account. For symmetric mixtures, the critical temperature T, is shown to deviate from its mean field value (approximately N) as square-root N, while the critical concentration remains unchanged in comparison to its mean field value phi(c) = 1/2. Since the fluctuations tend to disorder the system, the real value of the critical temperature is lower than its mean field value. For asymmetric A, B mixture (N(A) > N(B)), the critical concentration of A monomers phiBAR(c) is shown to be larger than its mean field value. In the limit of N(A) --> infinity, the critical temperature attains its mean field value, even for finite NB. However, we estimate that for N(A) = N(B) approximately 10(4), the correction to the Flory-Huggins parameter at the critical point may still be of the order of 10%, although it depends on the details of the system. The explicit formulas for T(c) and phiBAR(c) as functions of N(A) and N(B) are given. The role of the upper wave vector cutoff in these formulas is emphasized and its proper estimate is given. The loop expansion, viewed as an expansion in a small parameter, is correct as long as both NA and NB are much larger than unity and breaks down when any of these quantities becomes of the order of unity. The calculation of the Ginzburg region in the temperature-concentration plane is also given. It is based on the analysis of the scattering intensity. The comparison with the earlier estimates of the Ginzburg criterion (for temperature) is made.
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页码:4835 / 4844
页数:10
相关论文
共 26 条
  • [1] AMIT DJ, 1984, FIELD THEORY RENORMA, P87
  • [2] COLLECTIVE AND SINGLE-CHAIN CORRELATIONS NEAR THE BLOCK COPOLYMER ORDER-DISORDER TRANSITION
    BARRAT, JL
    FREDRICKSON, GH
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1991, 95 (02) : 1281 - 1289
  • [3] STATIC AND DYNAMIC CROSSOVER IN A CRITICAL POLYMER MIXTURE
    BATES, FS
    ROSEDALE, JH
    STEPANEK, P
    LODGE, TP
    WILTZIUS, P
    FREDRICKSON, GH
    HJELM, RP
    [J]. PHYSICAL REVIEW LETTERS, 1990, 65 (15) : 1893 - 1896
  • [4] NUCLEATION BARRIERS, SPINODALS, AND THE GINZBURG CRITERION
    BINDER, K
    [J]. PHYSICAL REVIEW A, 1984, 29 (01): : 341 - 349
  • [5] BRAZOVSKII SA, 1975, ZH EKSP TEOR FIZ, V41, P85
  • [6] SCREENING OF INTERACTIONS IN POLYMER BLENDS
    BRERETON, MG
    VILGIS, TA
    [J]. JOURNAL DE PHYSIQUE, 1989, 50 (03): : 245 - 253
  • [7] QUALITATIVE FEATURES OF POLYMER DEMIXTION
    DEGENNES, PG
    [J]. JOURNAL DE PHYSIQUE LETTRES, 1977, 38 (21): : L441 - L443
  • [8] DEGENNES PG, 1970, J PHYS-PARIS, V31, P235
  • [9] DEGENNES PG, 1979, SCALING CONCEPT POLY, P103
  • [10] DEGENNES PG, 1979, SCALING CONCEPTS POL, P114