Contribution to the Study of the Mean Square End-to-End Distance (rn2) of a Polymer Chain

1979 ◽  
Vol 12 (4) ◽  
pp. 713-715 ◽  
Author(s):  
Marguerite Lautout-Magat
2005 ◽  
Vol 19 (29) ◽  
pp. 4381-4387
Author(s):  
CHERDSAK KUNSOMBAT ◽  
VIRULH SA-YAKANIT

In this paper we consider the model of a flexible polymer chain embedded in a quenched random medium with long-range disorder correlations. Using the Feynman path integral approach we show that for the case of long-range quadratic correlations, we obtain an analytical result. The result is [Formula: see text], where 〈R2〉 is the mean square end-to-end distance of the polymer chain, ξ is the correlation length of disorder, Δ is an unknown parameter, b is the Kuhn step length, ρ is the density of random obstacles and N is the number of links. It is shown that for a polymer chain in a random media with long-range quadratic correlations, where ρ is not too high, the behavior of the polymer chain is like that of a free chain. This result agrees with the calculation using the replica method. However, in a medium where ρ is very high, the variation of the mean square end-to-end distance with disorder and its distance depending on ρ are found in our approach.


1980 ◽  
Vol 72 (4) ◽  
pp. 2702-2707 ◽  
Author(s):  
Ronnie Barr ◽  
Chava Brender ◽  
Melvin Lax

2013 ◽  
Vol 341-342 ◽  
pp. 195-198
Author(s):  
Lin Lin Cui ◽  
Hua Nan Guan

The author adopts Monte Carlo compute method to simulate the linear polymer chain lattice model in multiple chain systems of chain lengthn=20, 50, 100 while the volume fraction Φ=0.125, and makes a research on the variational situation of the size (measured with the mean-square end-to-end distance <R2> and the mean-square radius of gyration <S2>), shape (measured with the mean asphericity factor <A>) with changing of the interaction energy between solvent molecule and polymer chain segment molecule εPS. Results indicate <R2>, <S2> and <A> have the changing rules that they become small with the increase of the εPS


2021 ◽  
Vol 9 ◽  
Author(s):  
Pavel Castro-Villarreal ◽  
J. E. Ramírez

The conformational states of a semiflexible polymer enclosed in a volume V:=ℓ3 are studied as stochastic realizations of paths using the stochastic curvature approach developed in [Rev. E 100, 012503 (2019)], in the regime whenever 3ℓ/ℓp>1, where ℓp is the persistence length. The cases of a semiflexible polymer enclosed in a cube and sphere are considered. In these cases, we explore the Spakowitz–Wang–type polymer shape transition, where the critical persistence length distinguishes between an oscillating and a monotonic phase at the level of the mean-square end-to-end distance. This shape transition provides evidence of a universal signature of the behavior of a semiflexible polymer confined in a compact domain.


1987 ◽  
Vol 01 (01n02) ◽  
pp. 19-25 ◽  
Author(s):  
D.C. KHANDEKAR ◽  
K.V. BHAGWAT ◽  
F.W. WIEGEL

We point out that a formal analogy exists between the path integrals for the configuration sum of a polyelectrolyte and for the propagator of a polaron in a polar crystal. Using this analogy and some recent results in polaron theory we evaluate the mean square end-to-end distance <X2> of the polyelectroyte. It is shown that for large polymers the electrostatic interaction does not change the behaviour of <X2> from that of a free polymer.


2013 ◽  
Vol 734-737 ◽  
pp. 3141-3144
Author(s):  
Lin Lin Cui ◽  
Hua Nan Guan

The author adopts Monte Carlo compute method to simulate the linear polymer chain lattice model in multiple chain systems of different volume fraction Φ while chain lengthn=50, and makes a research on the variational situation of the size (measured with the mean-square end-to-end distance <R2> and the mean-square radius of gyration <S2>), shape (measured with the mean asphericity factor ) with changing of the interaction energy between solvent molecule and polymer chain segment moleculeεPS. Results indicate <R2>, <S2> and have the changing rules that they become small with the increase of theεPS.


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