Short-range order effects in amorphous polycondensates as studied by spin polarized diffuse neutron scattering and simulation

Short-range order effects in amorphous polycondensates, including the technologically important bisphenol-A-polycarbonate, have been investigated by elastic diffuse neutron scattering with spin polarization analysis. Selectively deuterated samples of each polycondensate have been used in order to vary the scattering contrast and thereby emphasize different pair correlations. The technique of spin polarization analysis allowed a reliable separation of the coherent scattering and an intensity calibration on the basis of the incoherent scattering as an internal standard. Thus, (d/d)_coh has been measured directly by this method. The experimental results are compared to calculated cross-sections from computer-generated structures. Simulations have been performed with the amorphous cell method which models the static structure of the amorphous polymer in full chemical detail on the basis of a random coil conformation. The results of the simulations yield a fertily ground for the discussion of the measured cross-sections, though a direct comparison with the experiment is not always satisfactory. The observed discrepancies indicate a still insufficient structural relaxation of the simulated structures.Dedicated to Professor Dr. E. W. Fischer of the occasion of his 65th birthday.     

Transport properties of highly ordered heterogeneous ion-exchange membranes

Model "ordered" heterogeneous ion exchange membranes are made with ion exchange particles heaving ion exchange capacity in the range 3 to 2.5 meq/gr (dry basis) and diameters ranging from 37 to 7 microm and 2 component room-temperature vulcanizing silicon rubber as a polymeric matrix, by applying an electric field normal to the membrane surface during preparation. These membranes were shown to have an improved ionic conductivity compared with "nonordered" membranes based on the same ion exchange content (for instance, at 10% resin content "nonordered" membranes show <10(-5) mS/cm while "ordered" membranes have conductivity of 1 mS/cm). The transport properties of ordered membranes were compared with those of nonordered membranes, through the current-voltage characteristics. Limiting currents measured for the ordered membranes were significantly higher than those of the nonordered membranes with the same resin concentration. In addition, higher limiting currents were observed in ordered membranes as the resin particles became smaller. Energy dispersion spectrometry analyses revealed that the concentration of cation exchange groups on the membrane surface was higher for ordered membrane as compared to that of nonordered membranes. This implies that the local current density for the conducting domains at the surface of the nonordered membranes is higher, leading to higher concentration polarization and, eventually, to lower average limiting current densities. The effect of ordering the particles on the membrane conductivity and transport properties was studied, and the advantages of the ordered membranes are discussed.