We present the complete (nonlinear) solution for the response of a system of living polymers to an arbitrary thermodynamic perturbation of its equilibrium polymer size distribution. Our result are relevant for the interpretation of T-jump experiments on wormlike micelles in the concentrated regime, where very large perturbations to the equilibrium size distribution can be easily obtained
We present predictions on the equilibrium behavior of solutions of living polymers confined in a gap...
The buckling of biopolymers is a frequently studied phenomenon The influence of thermal fluctuations...
International audienceThe steady state distribution of polymer (or micelle) lengths under nonequilbr...
We study theoretically the behaviour of a system of « living polymers » (polymers that can break and...
We report the first numeric experiments on the thermodynamic relaxation in living polymers (polymers...
We study theoretically the dynamics of living polymers which can add and subtract monomer units at t...
We investigate the thermodynamic properties of a dilute solution of living polymers confined between...
The molecular relaxation mechanisms of polymers with multi-scale units of motion in glassy, rubbery ...
The statistical mechanics and scission-recombination mechanism of self-assembling linear micelles ar...
A theoretical model, recently introduced to describe the dynamics of reversibly breakable polymer ch...
This paper analyzes the linear version of the theory of \u27\u27relaxation interactions\u27\u27 in p...
We present analytical results on the so-called end-evaporation kinetics in equilibrium polymeric sys...
A polymer-chain network is a collection of interconnected polymer-chains, made themselves of the rep...
A polymer-chain network is a collection of interconnected polymer-chains, made themselves of the rep...
We study the linear response of “living” systems, which break and recombine randomly. The mean field...
We present predictions on the equilibrium behavior of solutions of living polymers confined in a gap...
The buckling of biopolymers is a frequently studied phenomenon The influence of thermal fluctuations...
International audienceThe steady state distribution of polymer (or micelle) lengths under nonequilbr...
We study theoretically the behaviour of a system of « living polymers » (polymers that can break and...
We report the first numeric experiments on the thermodynamic relaxation in living polymers (polymers...
We study theoretically the dynamics of living polymers which can add and subtract monomer units at t...
We investigate the thermodynamic properties of a dilute solution of living polymers confined between...
The molecular relaxation mechanisms of polymers with multi-scale units of motion in glassy, rubbery ...
The statistical mechanics and scission-recombination mechanism of self-assembling linear micelles ar...
A theoretical model, recently introduced to describe the dynamics of reversibly breakable polymer ch...
This paper analyzes the linear version of the theory of \u27\u27relaxation interactions\u27\u27 in p...
We present analytical results on the so-called end-evaporation kinetics in equilibrium polymeric sys...
A polymer-chain network is a collection of interconnected polymer-chains, made themselves of the rep...
A polymer-chain network is a collection of interconnected polymer-chains, made themselves of the rep...
We study the linear response of “living” systems, which break and recombine randomly. The mean field...
We present predictions on the equilibrium behavior of solutions of living polymers confined in a gap...
The buckling of biopolymers is a frequently studied phenomenon The influence of thermal fluctuations...
International audienceThe steady state distribution of polymer (or micelle) lengths under nonequilbr...