160 research outputs found
Universality and its Origins at the Amorphous Solidification Transition
Systems undergoing an equilibrium phase transition from a liquid state to an
amorphous solid state exhibit certain universal characteristics. Chief among
these are the fraction of particles that are randomly localized and the scaling
functions that describe the order parameter and (equivalently) the statistical
distribution of localization lengths for these localized particles. The purpose
of this Paper is to discuss the origins and consequences of this universality,
and in doing so, three themes are explored. First, a replica-Landau-type
approach is formulated for the universality class of systems that are composed
of extended objects connected by permanent random constraints and undergo
amorphous solidification at a critical density of constraints. This formulation
generalizes the cases of randomly cross-linked and end-linked macromolecular
systems, discussed previously. The universal replica free energy is
constructed, in terms of the replica order parameter appropriate to amorphous
solidification, the value of the order parameter is obtained in the liquid and
amorphous solid states, and the chief universal characteristics are determined.
Second, the theory is reformulated in terms of the distribution of local static
density fluctuations rather than the replica order parameter. It is shown that
a suitable free energy can be constructed, depending on the distribution of
static density fluctuations, and that this formulation yields precisely the
same conclusions as the replica approach. Third, the universal predictions of
the theory are compared with the results of extensive numerical simulations of
randomly cross-linked macromolecular systems, due to Barsky and Plischke, and
excellent agreement is found.Comment: 10 pages, including 3 figures (REVTEX
One-step replica symmetry breaking solution of the quadrupolar glass model
We consider the quadrupolar glass model with infinite-range random
interaction. Introducing a simple one-step replica symmetry breaking ansatz we
investigate the para-glass continuous (discontinuous) transition which occurs
below (above) a critical value of the quadrupole dimension m*. By using a
mean-field approximation we study the stability of the one-step replica
symmetry breaking solution and show that for m>m* there are two transitions.
The thermodynamic transition is discontinuous but there is no latent heat. At a
higher temperature we find the dynamical or glass transition temperature and
the corresponding discontinuous jump of the order parameter.Comment: 10 pages, 3 figure
Goldstone fluctuations in the amorphous solid state
Goldstone modes in the amorphous solid state, resulting from the spontaneous
breaking of translational symmetry due to random localisation of particles, are
discussed. Starting from a microscopic model with quenched disorder, the broken
symmetry is identified to be that of relative translations of the replicas.
Goldstone excitations, corresponding to pure shear deformations, are
constructed from long wavelength distortions of the order parameter. The
elastic free energy is computed, and it is shown that Goldstone fluctuations
destroy localisation in two spatial dimensions, yielding a two-dimensional
amorphous solid state characterised by power-law correlations.Comment: 7 pages, 2 figure
Cavity Approach to the Random Solid State
The cavity approach is used to address the physical properties of random
solids in equilibrium. Particular attention is paid to the fraction of
localized particles and the distribution of localization lengths characterizing
their thermal motion. This approach is of relevance to a wide class of random
solids, including rubbery media (formed via the vulcanization of polymer
fluids) and chemical gels (formed by the random covalent bonding of fluids of
atoms or small molecules). The cavity approach confirms results that have been
obtained previously via replica mean-field theory, doing so in a way that sheds
new light on their physical origin.Comment: 4 pages, 2 figure
Elasticity near the vulcanization transition
Signatures of the vulcanization transition--amorphous solidification induced
by the random crosslinking of macromolecules--include the random localization
of a fraction of the particles and the emergence of a nonzero static shear
modulus. A semi-microscopic statistical-mechanical theory is presented of the
latter signature that accounts for both thermal fluctuations and quenched
disorder. It is found (i) that the shear modulus grows continuously from zero
at the transition, and does so with the classical exponent, i.e., with the
third power of the excess cross-link density and, quite surprisingly, (ii) that
near the transition the external stresses do not spoil the spherical symmetry
of the localization clouds of the particles.Comment: REVTEX, 5 pages. Minor change
Random solids and random solidification: What can be learned by exploring systems obeying permanent random constraints?
In many interesting physical settings, such as the vulcanization of rubber,
the introduction of permanent random constraints between the constituents of a
homogeneous fluid can cause a phase transition to a random solid state. In this
random solid state, particles are permanently but randomly localized in space,
and a rigidity to shear deformations emerges. Owing to the permanence of the
random constraints, this phase transition is an equilibrium transition, which
confers on it a simplicity (at least relative to the conventional glass
transition) in the sense that it is amenable to established techniques of
equilibrium statistical mechanics. In this Paper I shall review recent
developments in the theory of random solidification for systems obeying
permanent random constraints, with the aim of bringing to the fore the
similarities and differences between such systems and those exhibiting the
conventional glass transition. I shall also report new results, obtained in
collaboration with Weiqun Peng, on equilibrium correlations and
susceptibilities that signal the approach of the random solidification
transition, discussing the physical interpretation and values of these
quantities both at the Gaussian level of approximation and, via a
renormalization-group approach, beyond.Comment: Paper presented at the "Unifying Concepts in Glass Physics" workshop,
International Centre for Theoretical Physics, Trieste, Italy (September
15-18, 1999
On the relevance of percolation theory to the vulcanization transition
The relationship between vulcanization and percolation is explored from the
perspective of renormalized local field theory. We show rigorously that the
vulcanization and percolation correlation functions are governed by the same
Gell--Mann-Low renormalization group equation. Hence, all scaling aspects of
the vulcanization transition are reigned by the critical exponents of the
percolation universality class.Comment: 9 pages, 2 figure
Scaling of Entropic Shear Rigidity
The scaling of the shear modulus near the gelation/vulcanization transition
is explored heuristically and analytically. It is found that in a dense melt
the effective chains of the infinite cluster have sizes that scale sub-linearly
with their contour length. Consequently, each contributes k_B T to the
rigidity, which leads to a shear modulus exponent d\nu. In contrast, in phantom
elastic networks the scaling is linear in the contour length, yielding an
exponent identical to that of the random resistor network conductivity, as
predicted by de Gennes'. For non-dense systems, the exponent should cross over
to d\nu when the percolation length becomes much larger than the
density-fluctuation length.Comment: 4 pages, 2 eps figure
Conformations of Randomly Linked Polymers
We consider polymers in which M randomly selected pairs of monomers are
restricted to be in contact. Analytical arguments and numerical simulations
show that an ideal (Gaussian) chain of N monomers remains expanded as long as
M<<N; its mean squared end to end distance growing as r^2 ~ M/N. A possible
collapse transition (to a region of order unity) is related to percolation in a
one dimensional model with long--ranged connections. A directed version of the
model is also solved exactly. Based on these results, we conjecture that the
typical size of a self-avoiding polymer is reduced by the links to R >
(N/M)^(nu). The number of links needed to collapse a polymer in three
dimensions thus scales as N^(phi), with (phi) > 0.43.Comment: 6 pages, 3 Postscript figures, LaTe
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