Nature of the collapse transition in interacting self-avoiding trails

被引:7
|
作者
Oliveira, Tiago J. [1 ,4 ,5 ]
Stilck, Juergen F. [2 ,3 ]
机构
[1] Univ Fed Vicosa, Dept Fis, BR-36570900 Vicosa, MG, Brazil
[2] Univ Fed Fluminense, Inst Fis, Ave Litoranea S-N, BR-24210346 Niteroi, RJ, Brazil
[3] Univ Fed Fluminense, Natl Inst Sci & Technol Complex Syst, Ave Litoranea S-N, BR-24210346 Niteroi, RJ, Brazil
[4] Iowa State Univ Sci & Technol, US DOE, Ames Lab, Ames, IA 50011 USA
[5] Iowa State Univ Sci & Technol, Dept Phys & Astron, Ames, IA 50011 USA
关键词
COIL-GLOBULE TRANSITION; TRICRITICAL POINTS; SQUARE LATTICE; EQUILIBRIUM POLYMERIZATION; UNIVERSALITY CLASSES; BRANCHED POLYMERS; SULFUR SOLUTIONS; LIQUID SULFUR; DIMENSIONS; MONTE-CARLO;
D O I
10.1103/PhysRevE.93.012502
中图分类号
O35 [流体力学]; O53 [等离子体物理学];
学科分类号
070204 ; 080103 ; 080704 ;
摘要
We study the interacting self-avoiding trail (ISAT) model on a Bethe lattice of general coordination q and on a Husimi lattice built with squares and coordination q = 4. The exact grand-canonical solutions of the model are obtained, considering that up to K monomers can be placed on a site and associating a weight omega(i) with an i-fold visited site. Very rich phase diagrams are found with nonpolymerized, regular polymerized, and dense polymerized phases separated by lines (or surfaces) of continuous and discontinuous transitions. For a Bethe lattice with q = 4 and K = 2, the collapse transition is identified with a bicritical point and the collapsed phase is associated with the dense polymerized (solidlike) phase instead of the regular polymerized (liquidlike) phase. A similar result is found for the Husimi lattice, which may explain the difference between the collapse transition for ISATs and for interacting self-avoiding walks on the square lattice. For q = 6 and K = 3 (studied on the Bethe lattice only), a more complex phase diagram is found, with two critical planes and two coexistence surfaces, separated by two tricritical and two critical end-point lines meeting at a multicritical point. The mapping of the phase diagrams in the canonical ensemble is discussed and compared with simulational results for regular lattices.
引用
收藏
页数:12
相关论文
共 50 条
  • [31] Adsorption and collapse of self-avoiding walks and polygons in three dimensions
    Vrbova, T
    Whittington, SG
    JOURNAL OF PHYSICS A-MATHEMATICAL AND GENERAL, 1996, 29 (19): : 6253 - 6264
  • [32] CROSSOVER-BEHAVIOR FOR SELF-AVOIDING WALKS INTERACTING WITH A SURFACE
    ZHAO, DM
    LOOKMAN, T
    DEBELL, K
    PHYSICAL REVIEW A, 1990, 42 (08): : 4591 - 4600
  • [33] New Monte Carlo algorithms for interacting self-avoiding walks
    Nidras, PP
    Brak, R
    JOURNAL OF PHYSICS A-MATHEMATICAL AND GENERAL, 1997, 30 (05): : 1457 - 1469
  • [34] Supermultiplicative relations in models of interacting self-avoiding walks and polygons
    van Rensburg, E. J. Janse
    JOURNAL OF PHYSICS A-MATHEMATICAL AND THEORETICAL, 2021, 54 (10)
  • [35] Exact Partition Functions of Interacting Self-Avoiding Walks on Lattices
    Hsieh, Yu-Hsin
    Chen, Chi-Ning
    Hu, Chin-Kun
    MATHEMATICAL MODELING AND COMPUTATIONAL PHYSICS (MMCP 2015), 2016, 108
  • [36] Grand canonical simulations of the interacting self-avoiding walk model
    Nidras, PP
    JOURNAL OF PHYSICS A-MATHEMATICAL AND GENERAL, 1996, 29 (24): : 7929 - 7942
  • [37] Interacting partially directed self-avoiding walk: a probabilistic perspective
    Carmona, Philippe
    Gia Bao Nguyen
    Petrelis, Nicolas
    Torri, Niccolo
    JOURNAL OF PHYSICS A-MATHEMATICAL AND THEORETICAL, 2018, 51 (15)
  • [38] Critical behaviour of the bond-interacting self-avoiding walk
    Foster, D. P.
    JOURNAL OF PHYSICS A-MATHEMATICAL AND THEORETICAL, 2007, 40 (09) : 1963 - 1980
  • [39] Grand-canonical solution of semiflexible self-avoiding trails on the Bethe lattice
    Dantas, W. G.
    Oliveira, Tiago J.
    Stilck, Jurgen F.
    Prellberg, Thomas
    PHYSICAL REVIEW E, 2017, 95 (02)
  • [40] ON THE CONFORMATIONAL TRANSITION OF A SELF-AVOIDING WALK ADSORBED AT AN INTERFACE
    BELLEMANS, A
    ORBAN, J
    JOURNAL OF CHEMICAL PHYSICS, 1981, 75 (05): : 2454 - 2461