ترغب بنشر مسار تعليمي؟ اضغط هنا

Distance dependence of angular correlations in dense polymer solutions

145   0   0.0 ( 0 )
 نشر من قبل J. P. Wittmer
 تاريخ النشر 2009
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

Angular correlations in dense solutions and melts of flexible polymer chains are investigated with respect to the distance $r$ between the bonds by comparing quantitative predictions of perturbation calculations with numerical data obtained by Monte Carlo simulation of the bond-fluctuation model. We consider both monodisperse systems and grand-canonical (Flory-distributed) equilibrium polymers. Density effects are discussed as well as finite chain length corrections. The intrachain bond-bond correlation function $P(r)$ is shown to decay as $P(r) sim 1/r^3$ for $xi ll r ll r^*$ with $xi$ being the screening length of the density fluctuations and $r^* sim N^{1/3}$ a novel length scale increasing slowly with (mean) chain length $N$.



قيم البحث

اقرأ أيضاً

The scaling of the bond-bond correlation function $C(s)$ along linear polymer chains is investigated with respect to the curvilinear distance, $s$, along the flexible chain and the monomer density, $rho$, via Monte Carlo and molecular dynamics simula tions. % Surprisingly, the correlations in dense three dimensional solutions are found to decay with a power law $C(s) sim s^{-omega}$ with $omega=3/2$ and the exponential behavior commonly assumed is clearly ruled out for long chains. % In semidilute solutions, the density dependent scaling of $C(s) approx g^{-omega_0} (s/g)^{-omega}$ with $omega_0=2-2 u=0.824$ ($ u=0.588$ being Florys exponent) is set by the number of monomers $g(rho)$ contained in an excluded volume blob of size $xi$. % Our computational findings compare well with simple scaling arguments and perturbation calculation. The power-law behavior is due to self-interactions of chains on distances $s gg g$ caused by the connectivity of chains and the incompressibility of the melt. %
60 - M. Watzlawek 1998
The core-core structure factor of dense star polymer solutions in a good solvent is shown theoretically to exhibit an unusual behaviour above the overlap concentration. Unlike usual liquids, these solutions display a structure factor whose first peak decreases by increasing density while the second peak grows. The scenario repeats itself with the subsequent peaks as the density is further enhanced. For low enough arm numbers $f$ ($f leq 32$), various different considerations lead to the conclusion that the system remains fluid at all concentrations.
By Monte Carlo simulations of a variant of the bond-fluctuation model without topological constraints we examine the center-of-mass (COM) dynamics of polymer melts in $d=3$ dimensions. Our analysis focuses on the COM displacement correlation function $CN(t) approx partial_t^2 MSDcmN(t)/2$, measuring the curvature of the COM mean-square displacement $MSDcmN(t)$. We demonstrate that $CN(t) approx -(RN/TN)^2 (rhostar/rho) f(x=t/TN)$ with $N$ being the chain length ($16 le N le 8192$), $RNsim N^{1/2}$ the typical chain size, $TNsim N^2$ the longest chain relaxation time, $rho$ the monomer density, $rhostar approx N/RN^d$ the self-density and $f(x)$ a universal function decaying asymptotically as $f(x) sim x^{-omega}$ with $omega = (d+2) times alpha$ where $alpha = 1/4$ for $x ll 1$ and $alpha = 1/2$ for $x gg 1$. We argue that the algebraic decay $N CN(t) sim - t^{-5/4}$ for $t ll TN$ results from an interplay of chain connectivity and melt incompressibility giving rise to the correlated motion of chains and subchains.
253 - M. Watzlawek , C. N. Likos , 1999
The phase diagram of star polymer solutions in a good solvent is obtained over a wide range of densities and arm numbers by Monte Carlo simulations. The effective interaction between the stars is modeled by an ultrasoft pair potential which is logari thmic in the core-core distance. Among the stable phases are a fluid as well as body-centered cubic, face-centered cubic, body-centered orthogonal, and diamond crystals. In a limited range of arm numbers, reentrant melting and reentrant freezing transitions occur for increasing density.
It is widely believed that the swimming speed, $v$, of many flagellated bacteria is a non-monotonic function of the concentration, $c$, of high-molecular-weight linear polymers in aqueous solution, showing peaked $v(c)$ curves. Pores in the polymer s olution were suggested as the explanation. Quantifying this picture led to a theory that predicted peaked $v(c)$ curves. Using new, high-throughput methods for characterising motility, we have measured $v$, and the angular frequency of cell-body rotation, $Omega$, of motile Escherichia coli as a function of polymer concentration in polyvinylpyrrolidone (PVP) and Ficoll solutions of different molecular weights. We find that non-monotonic $v(c)$ curves are typically due to low-molecular weight impurities. After purification by dialysis, the measured $v(c)$ and $Omega(c)$ relations for all but the highest molecular weight PVP can be described in detail by Newtonian hydrodynamics. There is clear evidence for non-Newtonian effects in the highest molecular weight PVP solution. Calculations suggest that this is due to the fast-rotating flagella `seeing a lower viscosity than the cell body, so that flagella can be seen as nano-rheometers for probing the non-Newtonian behavior of high polymer solutions on a molecular scale.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا