Four-dimensional polymer collapse II: Interacting self-avoiding trails

We have simulated four-dimensional interacting self-avoiding trails (ISAT) on the hyper-cubic lattice with standard interactions at a wide range of temperatures up to length 4096 and at some temperatures up to length 16384. The results confirm the earlier prediction (using data from a non-standard model at a single temperature) of a collapse phase transition occurring at finite temperature. Moreover they are in accord with the phenomenological theory originally proposed by Lifshitz, Grosberg and Khokhlov in three dimensions and recently given new impetus by its use in the description of simulational results for four-dimensional interacting self-avoiding walks (ISAW). In fact, we argue that the available data is consistent with the conclusion that the collapse transitions of ISAT and ISAW lie in the same universality class, in contradiction with long-standing predictions. We deduce that there exists a pseudo-first order transition for ISAT in four dimensions at finite lengths while the thermodynamic limit is described by the standard polymer mean-field theory (giving a second-order transition), in contradiction to the prediction that the upper critical dimension for ISAT is $d_u=4$.Comment: 23 pages, 8 figure

Collapse transition of self-avoiding trails on the square lattice

The collapse transition of an isolated polymer has been modelled by many different approaches, including lattice models based on self-avoiding walks and self-avoiding trails. In two dimensions, previous simulations of kinetic growth trails, which map to a particular temperature of interacting self-avoiding trails, showed markedly different behaviour for what was argued to be the collapse transition than that which has been verified for models based of self-avoiding walks. On the other hand, it has been argued that kinetic growth trails represent a special simulation that does not give the correct picture of the standard equilibrium model. In this work we simulate the standard equilibrium interacting self-avoiding trail model on the square lattice up to lengths over $2,000,000$ steps and show that the results of the kinetic growth simulations are, in fact, entirely in accord with standard simulations of the temperature dependent model. In this way we verify that the collapse transition of interacting self-avoiding walks and trails are indeed in different universality classes in two dimensions

Critical Percolation in High Dimensions

We present Monte Carlo estimates for site and bond percolation thresholds in simple hypercubic lattices with 4 to 13 dimensions. For d<6 they are preliminary, for d >= 6 they are between 20 to 10^4 times more precise than the best previous estimates. This was achieved by three ingredients: (i) simple and fast hashing which allowed us to simulate clusters of millions of sites on computers with less than 500 MB memory; (ii) a histogram method which allowed us to obtain information for several p values from a single simulation; and (iii) a new variance reduction technique which is especially efficient at high dimensions where it reduces error bars by a factor up to approximately 30 and more. Based on these data we propose a new scaling law for finite cluster size corrections.Comment: 5 pages including figures, RevTe

Stretched Polymers in a Poor Solvent

Stretched polymers with attractive interaction are studied in two and three dimensions. They are described by biased self-avoiding random walks with nearest neighbour attraction. The bias corresponds to opposite forces applied to the first and last monomers. We show that both in $d=2$ and $d=3$ a phase transition occurs as this force is increased beyond a critical value, where the polymer changes from a collapsed globule to a stretched configuration. This transition is second order in $d=2$ and first order in $d=3$. For $d=2$ we predict the transition point quantitatively from properties of the unstretched polymer. This is not possible in $d=3$, but even there we can estimate the transition point precisely, and we can study the scaling at temperatures slightly below the collapse temperature of the unstretched polymer. We find very large finite size corrections which would make very difficult the estimate of the transition point from straightforward simulations.Comment: 10 pages, 16 figure

Order Parameters of the Dilute A Models

The free energy and local height probabilities of the dilute A models with broken \Integer_2 symmetry are calculated analytically using inversion and corner transfer matrix methods. These models possess four critical branches. The first two branches provide new realisations of the unitary minimal series and the other two branches give a direct product of this series with an Ising model. We identify the integrable perturbations which move the dilute A models away from the critical limit. Generalised order parameters are defined and their critical exponents extracted. The associated conformal weights are found to occur on the diagonal of the relevant Kac table. In an appropriate regime the dilute A$_3$ model lies in the universality class of the Ising model in a magnetic field. In this case we obtain the magnetic exponent $\delta=15$ directly, without the use of scaling relations.Comment: 53 pages, LaTex, ITFA 93-1

Mechanical unfolding of directed polymers in a poor solvent: Critical exponents

We study the thermodynamics of an exactly solvable model of a self-interacting, partially directed self-avoiding walk in two dimensions when a force is applied on one end of the chain. The critical force for the unfolding is determined exactly, as a function of the temperature, below the Theta transition. The transition is of second order and is characterized by new critical exponents that are determined by a careful numerical analysis. The usual polymer critical index nu on the critical line, and another one which we call zeta, takes a nontrivial value that is numerically close to 2/3