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Register a new userUniversality classes of dense polymers and conformal sigma models
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In the usual statistical model of a dense polymer (a single space-filling loop on a lattice) in two dimensions the loop does not cross itself. We modify this by including intersections in which {em three} lines can cross at the same point, with some statistical weight w per crossing. We show that our model describes a line of critical theories with continuously-varying exponents depending on w, described by a conformally-invariant non-linear sigma model with varying coupling constant g_sigma^2 >0. For the boundary critical behavior, or the model defined in a strip, we propose an exact formula for the ell-leg exponents, h_ell=g_sigma^2 ell(ell-2)/8, which is shown numerically to hold very well.
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We study the conditions under which the critical behavior of the three-dimensional $mn$-vector model does not belong to the spherically symmetrical universality class. In the calculations we rely on the field-theoretical renormalization group approach in different regularization schemes adjusted by resummation and extended analysis of the series for renormalization-group functions which are known for the model in high orders of perturbation theory. The phase diagram of the three-dimensional $mn$-vector model is built marking out domains in the $mn$-plane where the model belongs to a given universality class.
We introduce a class of information measures based on group entropies, allowing us to describe the information-theoretical properties of complex systems. These entropic measures are nonadditive, and are mathematically deduced from a series of natural requirements. In particular, we introduce an extensivity postulate as a natural requirement for an information measure to be meaningful. The information measures proposed are suitably defined for describing universality classes of complex systems, each characterized by a specific phase space growth rate function.
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Recently, it has been proposed that the adsorption transition for a single polymer in dilute solution, modeled by lattice walks in three dimensions, is not universal with respect to inter-monomer interactions. It has also been conjectured that key critical exponents $phi$, measuring the growth of the contacts with the surface at the adsorption point, and $1/delta$, which measures the finite-size shift of the critical temperature, are not the same. However, applying standard scaling arguments the two key critical exponents should be identical, thus pointing to a potential breakdown of these standard scaling arguments. This is in contrast to the well studied situation in two dimensions, where there are exact results from conformal field theory: these exponents are both accepted to be $1/2$ and universal. We use the flatPERM algorithm to simulate self-avoiding walks and trails on the hexagonal, square and simple cubic lattices up to length $1024$ to investigate these claims. Walks can be seen as a repulsive limit of inter-monomer interaction for trails, allowing us to probe the universality of adsorption. For each model we analyze several thermodynamic properties to produce different methods of estimating the critical temperature and the key exponents. We test our methodology on the two-dimensional cases and the resulting spread in values for $phi$ and $1/delta$ indicates that there is a systematic error that exceeds the statistical error usually reported. We further suggest a methodology for consistent estimation of the key adsorption exponents which gives $phi=1/delta=0.484(4)$ in three dimensions. We conclude that in three dimensions these critical exponents indeed differ from the mean-field value of $1/2$, but cannot find evidence that they differ from each other. Importantly, we also find no substantive evidence of any non-universality in the polymer adsorption transition.
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