We report a new type of step‐growth radical addition‐coupling polymerization (RACP) involving consecutive addition of carbon‐centered radical derived from α,α′‐dibromo dibasic ester to NO double bond of C‐nitroso compound followed by cross‐coupling of carbon‐centered radical and in situ formed nitroxyl radical, which produces alternating copolymers with high molecular weight and unimodal molecular weight distribution from saturated and unsaturated monomers.
Bimodal fiber meshes with fiber diameters differing by one order of magnitude, are electrospun in a simple one‐step process, using a standard single syringe electrospin setup. The nano‐ and microfiber meshes combine the benefits of nanofibers (cell adhesion, proliferation) with those of microfibers (open structure, large pore size) and are therefore interesting as scaffolds for cellular infiltration.
Summary: The effect of melt memory on shear‐induced crystallization of a low‐density polyethylene melt is evaluated with a new shear DTA instrument. A critical strain is identified as the controlling factor for saturating the crystallization. Variation of this strain with the temperature of the sheared melt is established, and the melt state responsible for saturating the crystallization is identified by shear‐stress growth experiments at the steady‐state. Reptation times have been evaluated in both viscoelastic nonlinear and linear regimes, and it is shown that small‐angle oscillatory shear experiments cannot be used to probe effectively the effect of shear flow on the overall crystallization kinetics.
Summary: Shear‐induced orientation of nanoparticles in poly(ethylene oxide)/Laponite RD hydrogels has been investigated by small angle neutron scattering (SANS). As temperature is reduced, anisotropy develops at lower shear rates. The two‐correlation length Debye–Anderson–Brumberger (DAB) model provides a good fit to the experimental data. The deduced short‐range correlation length (≈5 nm) is observed to increase with shear. The long‐range correlation length (≈50 nm) shows a strong directional dependence, and decreases when shear is applied. The relative contribution of long‐range order to the SANS intensity is observed to increase with shear and decrease with temperature.
SANS anisotropy |(Iy − Ix)/(Iy + Ix)| as a function of shear rate and q at 2 °C. 相似文献
The phase diagram of a series of poly(1,2‐octylene oxide)–poly(ethylene oxide) (POO–PEO) diblock copolymers is determined by small‐angle X‐ray scattering. The Flory–Huggins interaction parameter was measured by small‐angle neutron scattering. The phase diagram is highly asymmetric due to large conformational asymmetry that results from the hexyl side chains in the POO block. Non‐lamellar phases (hexagonal and gyroid) are observed near fPEO = 0.5, and the lamellar phase is observed for fPEO ≥ 0.5.
A simple approach to tune the optical properties of the hyperbranched conjugated polymers by only adjusting the terminal‐backbone interactions has been reported in this article. Hyperbranched conjugated polyazomethines have been successfully prepared by the reaction of tetramine and dialdehyde. Not only varying the monomer feed ratio to change the quantity of terminal amino groups, but also adopting protonation or complexion with proper dopants (SnCl2 and β‐cyclodextrin), can alter the interactions between amino terminals and imine bonds in the backbone. Correspondingly, the optical properties of the resulting hyperbranched polymers are controlled.
