Thermally activated breakdown in a simple polymer model

We consider the thermally activated fragmentation of a homopolymer chain. In our simple model the dynamics of the intact chain is a Rouse one until a bond breaks and bond breakdown is considered as a first passage problem over a barrier to an absorbing boundary. Using the framework of the Wilemski-Fixman approximation we calculate activation times of individual bonds for free and grafted chains. We show that these times crucially depend on the length of the chain and the location of the bond yielding a minimum at the free chain ends. Theoretical findings are qualitatively confirmed by Brownian dynamics simulations

Classification of graph C*-algebras with no more than four primitive ideals

We describe the status quo of the classification problem of graph C*-algebras with four primitive ideals or less

A practical density functional for polydisperse polymers

The Flory Huggins equation of state for monodisperse polymers can be turned into a density functional by adding a square gradient term, with a coefficient fixed by appeal to RPA (random phase approximation). We present instead a model nonlocal functional in which each polymer is replaced by a deterministic, penetrable particle of known shape. This reproduces the RPA and square gradient theories in the small deviation and/or weak gradient limits, and can readily be extended to polydisperse chains. The utility of the new functional is shown for the case of a polydisperse polymer solution at coexistence in a poor solvent.Comment: 9 pages, 3 figure

Accurate statistics of a flexible polymer chain in shear flow

We present exact and analytically accurate results for the problem of a flexible polymer chain in shear flow. Under such a flow the polymer tumbles, and the probability distribution of the tumbling times $\tau$ of the polymer decays exponentially as $\sim \exp(-\alpha \tau/\tau_0)$ (where $\tau_0$ is the longest relaxation time). We show that for a Rouse chain, this nontrivial constant $\alpha$ can be calculated in the limit of large Weissenberg number (high shear rate) and is in excellent agreement with our simulation result of $\alpha \simeq 0.324$. We also derive exactly the distribution functions for the length and the orientational angles of the end-to-end vector of the polymer.Comment: 4 pages, 2 figures. Minor changes. Texts differ slightly from the PRL published versio

CSIP - a Novel Photon-Counting Detector Applicable for the SPICA Far-Infrared Instrument

We describe a novel GaAs/AlGaAs double-quantum-well device for the infrared photon detection, called Charge-Sensitive Infrared Phototransistor (CSIP). The principle of CSIP detector is the photo-excitation of an intersubband transition in a QW as an charge integrating gate and the signal amplification by another QW as a channel with very high gain, which provides us with extremely high responsivity (10^4 -- 10^6 A/W). It has been demonstrated that the CSIP designed for the mid-infrared wavelength (14.7 um) has an excellent sensitivity; the noise equivalent power (NEP) of 7x10^-19 W/rHz with the quantum efficiency of ~2%. Advantages of the CSIP against the other highly sensitive detectors are, huge dynamic range of >10^6, low output impedance of 10^3 -- 10^4 Ohms, and relatively high operation temperature (>2K). We discuss possible applications of the CSIP to FIR photon detection covering 35 -- 60 um waveband, which is a gap uncovered with presently available photoconductors.Comment: To appear in Proc. Workshop "The Space Infrared Telescope for Cosmology & Astrophysics: Revealing the Origins of Planets and Galaxies". Eds. A.M. Heras, B. Swinyard, K. Isaak, and J.R. Goicoeche

The stochastic pump current and the non-adiabatic geometrical phase

We calculate a pump current in a classical two-state stochastic chemical kinetics by means of the non-adiabatic geometrical phase interpretation. The two-state system is attached to two particle reservoirs, and under a periodic perturbation of the kinetic rates, it gives rise to a pump current between the two-state system and the absorbing states. In order to calculate the pump current, the Floquet theory for the non-adiabatic geometrical phase is extended from a Hermitian case to a non-Hermitian case. The dependence of the pump current on the frequency of the perturbative kinetic rates is explicitly derived, and a stochastic resonance-like behavior is obtained.Comment: 11 page

Reaction-diffusion processes and non-perturbative renormalisation group

This paper is devoted to investigating non-equilibrium phase transitions to an absorbing state, which are generically encountered in reaction-diffusion processes. It is a review, based on [Phys. Rev. Lett. 92, 195703; Phys. Rev. Lett. 92, 255703; Phys. Rev. Lett. 95, 100601], of recent progress in this field that has been allowed by a non-perturbative renormalisation group approach. We mainly focus on branching and annihilating random walks and show that their critical properties strongly rely on non-perturbative features and that hence the use of a non-perturbative method turns out to be crucial to get a correct picture of the physics of these models.Comment: 14 pages, submitted to J. Phys. A for the proceedings of the conference 'Renormalization Group 2005', Helsink

Analog of Astrophysical Magnetorotational Instability in a Couette-Taylor Flow of Polymer Fluids

We report experimental observation of an instability in a Couette-Taylor flow of a polymer fluid in a thin gap between two coaxially rotating cylinders in a regime where their angular velocity decreases with the radius while the specific angular momentum increases with the radius. In the considered regime, neither the inertial Rayleigh instability nor the purely elastic instability are possible. We propose that the observed "elasto-rotational" instability is an analog of the magnetorotational instability which plays a fundamental role in astrophysical Keplerian accretion disks.Comment: 4 pages, 1 figur

Slow plasmon modes in polymeric salt solutions

The dynamics of polymeric salt solutions are presented. The salt consists of chains $\rm A$ and $\rm B$, which are chemically different and interact with a Flory-interaction parameter $\chi$, the $\rm A$ chain ends carry a positive charge whereas the $\rm B$ chain ends are modified by negative charges. The static structure factor shows a peak corresponding to a micro phase separation. At low momentum transfer, the interdiffusion mode is driven by electrostatics and is of the plasmon-type, but with an unusually low frequency, easily accessible by experiments. This is due to the polymer connectivity that introduces high friction and amplifies the charge scattering thus allowing for low charge densities. The interdiffusion mode shows a minimum (critical slowing down) at finite $k$ when the interaction parameter increases we find then a low $k$ frequency quasi-plateau.Comment: accepted in Europhys. Let