Continuous transition of colloidal crystals through stable random orders.

Randomly stacked 2D hexagonal close-packed (RHCP) layer structures are frequently observed in colloids and other material systems but are considered metastable. We report a stable RHCP phase domain of poly(butadiene-b-ethylene oxide) (PB-PEO) diblock copolymer micellar colloids in water. The stable RHCP colloidal crystals emerge in the middle of a continuously transiting phase domain of close-packed PB-PEO colloids from a face-centered cubic (FCC) polytype to a HCP polytype. We attribute the stability of RHCP structures to two competing contributions, entropic preference for FCC lattices and long PEO corona chains stabilizing HCP lattices. When these two contributions become comparable in the phase space, thermal fluctuation randomizes the stacking order of the 2D-HCP layers, and RHCP orders are stabilized. The continuously transiting close-packed structures of PB-PEO colloids with stable RHCP states suggest that similar structural transitions and equivalent RHCP states may occur in other polytypic crystal systems because polytypic crystals have the common crystal construction rule, i.e., stacking 2D-HCP lattice layer groups in different orders.

Tuneable phase behaviour and glass transition via polymerization-induced phase separation in crosslinked step-growth polymers.

Once limited to chain-growth polymerizations, fine control over polymerization-induced phase separation (PIPS) has recently been demonstrated in rubber-toughened thermoset materials formed through step-growth polymerizations. The domain length scales of these thermoset materials can be elegantly tuned by utilizing a binary mixture of curing agents (CAs) that individually yield disparate morphologies. Importantly, varying the composition of the binary mixture affects characteristics of the materials such as glass transition temperature and tensile behavior. Here, we establish a full phase diagram of PIPS in a rubber-toughened epoxy system tuned by a binary CA mixture to provide a robust framework of phase behaviour. X-Ray scattering in situ and post-PIPS is employed to elucidate the PIPS mechanism whereby an initial polymerization-induced compositional fluctuation causes nanoscale phase separation of rubber and epoxy components prior to local chain crosslinking and potential macrophase separation. We further demonstrate the universality of this approach by alternatively employing binary epoxy or binary rubber mixtures to achieve broad variations in morphology and glass transitions.

Network structure and enzymatic degradation of chitosan hydrogels determined by crosslinking methods.

Polysaccharides can be modified by reactive functional groups to enable chemical crosslinking. We studied how different methods of crosslinking methacrylate-functionalized chitosan affected the network structures and various properties relevant for utilization of the chemically crosslinked hydrogels in biomedical applications, including tissue engineering and delivery of therapeutic agents. Four chitosan hydrogels were made by either the free radical polymerization with varying initiation kinetics and an addition of chain transfer agents or the based-catalyzed Michael-type addition reaction. Four chitosan hydrogels having identical polymer fractions at equilibrium swelling exhibited marked differences in shear moduli, dextran diffusion rate, and especially enzymatic degradation behaviors. Hydrogels made by the free radical polymerization with no chain transfer agent were highly resistant to complete degradation by enzyme for an extended period. We inferred that such resistance originated from chain bundles characterized by densely branched networks of chitosan chains, which was determined by small-angle X-ray scattering analysis.