Loops in One Dimensional Random Walks

Distribution of loops in a one-dimensional random walk (RW), or, equivalently, neutral segments in a sequence of positive and negative charges is important for understanding the low energy states of randomly charged polymers. We investigate numerically and analytically loops in several types of RWs, including RWs with continuous step-length distribution. We show that for long walks the probability density of the longest loop becomes independent of the details of the walks and definition of the loops. We investigate crossovers and convergence of probability densities to the limiting behavior, and obtain some of the analytical properties of the universal probability density.Comment: 9 two-column pages. 8 eps figures. RevTex. Submitted to Eur. Phys. J.

Attractive and repulsive polymer-mediated forces between scale-free surfaces

We consider forces acting on objects immersed in, or attached to, long fluctuating polymers. The confinement of the polymer by the obstacles results in polymer-mediated forces that can be repulsive (due to loss of entropy) or attractive (if some or all surfaces are covered by adsorbing layers). The strength and sign of the force in general depends on the detailed shape and adsorption properties of the obstacles, but assumes simple universal forms if characteristic length scales associated with the objects are large. This occurs for scale-free shapes (such as a flat plate, straight wire, or cone), when the polymer is repelled by the obstacles, or is marginally attracted to it (close to the depinning transition where the absorption length is infinite). In such cases, the separation $h$ between obstacles is the only relevant macroscopic length scale, and the polymer mediated force equals ${\cal A} \, k_{B}T/h$, where $T$ is temperature. The amplitude ${\cal A}$ is akin to a critical exponent, depending only on geometry and universality of the polymer system. The value of ${\cal A}$, which we compute for simple geometries and ideal polymers, can be positive or negative. Remarkably, we find ${\cal A}=0$ for ideal polymers at the adsorption transition point, irrespective of shapes of the obstacles, i.e. at this special point there is no polymer-mediated force between obstacles (scale-free or not).Comment: RevTeX, 10 pages, 10 figure

Entropic Elasticity at the Sol-Gel Transition

The sol-gel transition is studied in two purely entropic models consisting of hard spheres in continuous three-dimensional space, with a fraction $p$ of nearest neighbor spheres tethered by inextensible bonds. When all the tethers are present ($p=1$) the two systems have connectivities of simple cubic and face-centered cubic lattices. For all $p$ above the percolation threshold $p_c$, the elasticity has a cubic symmetry characterized by two distinct shear moduli. When $p$ approaches $p_c$, both shear moduli decay as $(p-p_c)^f$, where $f\simeq 2$ for each type of the connectivity. This result is similar to the behavior of the conductivity in random resistor networks, and is consistent with many experimental studies of gel elasticity. The difference between the shear moduli that measures the deviation from isotropy decays as $(p-p_c)^h$, with $h\simeq 4$.Comment: 12 pages, 3 eps figures, RevTe