Condensation modes in magnetized plasmas

Condensation modes in magnetized cylindrical plasmas, with concentration on how magnetic field affects the stability were studied. It is found that the effects of magnetic field (shear, twist, and strength) on the condensation modes are different depending on the wave vector. For modes whose wave vector is not perpendicular to magnetic field lines the plasma motion is mainly along the field lines; the effects of magnetic field on the modes are negligible except on the heat flow parallel to the field line. For a mode which is localized near a surface where the wave vector is perpendicular to the field line, the plasma moves perpendicular to the line carrying the field line into the condensed region; magnetic field affects the mode by building up magnetic pressure in the condensed region. The stability of condensation modes strongly depends on how density and temperature vary with field twist. The stable nature of global quiescent prominence magnetic configurations implies that prominences form for low field twist for which ideal MHD modes are stable; plasma temperature should increase with field twist for stable prominence formation

Self-consistent field theory of polymer-ionic molecule complexation

A self-consistent field theory is developed for polymers that are capable of binding small ionic molecules (adsorbates). The polymer-ionic molecule association is described by Ising-like binding variables, C_(i)^(a)(kΔ)(= 0 or 1), whose average determines the number of adsorbed molecules, nBI. Polymer gelation can occur through polymer-ionic molecule complexation in our model. For polymer-polymer cross-links through the ionic molecules, three types of solutions for nBI are obtained, depending on the equilibrium constant of single-ion binding. Spinodal lines calculated from the mean-field free energy exhibit closed-loop regions where the homogeneous phase becomes unstable. This phase instability is driven by the excluded-volume interaction due to the single occupancy of ion-binding sites on the polymers. Moreover, sol-gel transitions are examined using a critical degree of conversion. A gel phase is induced when the concentration of adsorbates is increased. At a higher concentration of the adsorbates, however, a re-entrance from a gel phase into a sol phase arises from the correlation between unoccupied and occupied ion-binding sites. The theory is applied to a model system, poly(vinyl alcohol) and borate ion in aqueous solution with sodium chloride. Good agreement between theory and experiment is obtaine

Phase Separation Induced by Ladder-Like Polymer-Polymer Complexation

Polymer-polymer complexation in solvent is studied using an extension of the self-consistent field theory. The model polymers are capable of forming ladder-like duplex structures. The duplex formation occurs with an abrupt change of entropy, resulting in a first-order transition. Moreover, the complexation can be stabilized by solvent-polymer interactions, instead of the usual specific binding interactions. Various types of unconventional phase diagrams are predicted. For example, phase separation with decreasing χ-parameter between duplex polymer and solvent can be induced, leading to a lower critical solution temperature (LCST) behavior. Multiphase coexistence points at which two, three, or four phases coexist are also obtained. Under certain conditions a homogeneous phase becomes unstable when the polymer chain length is decreased, in contrast to the standard Flory-Huggins theory