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In a systematic manner, the roles of MWNTs as filler and styrene acrylonitrile copolymer-graft-maleic anhydride (SAN-MA) as compatibilizer, individually and together, on dynamic-mechanical behavior of polycarbonate (PC)-rich/ acrylonitrile butadiene styrene terpolymer (ABS) blend were studied. The investigations were performed using small-scale mixing in a one-step procedure with a fixed MWNTs content of 0.75 wt% and a blend composition of PC/ABS = 70/30 w/w. PC/SAN blends and nanocomposites as simpler model system for PC/ABS were also studied to reveal the role of the rubbery polybutadiene (PB) fraction. It is found that the tendency of MWNTs to localize within the PC component in compatibilized PC/ABS was lower than in compatibilized PC/SAN blends. Dynamic mechanical analysis (DMA) revealed the dual role of SAN-MA as blend compatibilizer and also promoter of MWNTs migration towards PC, where SAN-MA to MWNTs weight ratio varied between 1 and 4. At the compatibilizer/MWNTs weight ratio of 1, MWNTs localized in PC component of the blends whereas increasing the compatibilizer/MWNTs ratio to 4 led to migration of MWNTs toward SAN or ABS component. In DMA studies, loss modulus normalization of the nanocomposites revealed the coexistence of mobilized and immobilized regions within the nanocomposite structure, as a result of MWNTs and compatibilizer loading., INTRODUCTION Fillers play an essential role to adjust the polymers' advantageous characteristics to reach the property balance needed for certain applications. It is expected that high aspect ratio as well [...]

Ultraviolet (UV) irradiated supramolecularpolybutadienes (PBs)containing 2-ureido-4-[1H]-pyrimidone (UPy) linkageswere examined as a simple model for curable supramolecular elastomers.Via precise control of UV exposure, the cure and the degradation ofthe vinyl groups within the PB elastomeric core were investigated.The combination of UPy binding and covalent cross-linking by UV irradiationdramatically enhanced mechanical properties of these UPy-functionalizedelastomers, yielding toughness enhancement up to ∼200×at the 5 min UV cure. UV-initiated cross-linking dominated the curingprocess up to ∼50 min exposure time. Beyond this cure time,dominant degradation of the vinyl linkages was observed. Control ofthis UV-initiated process yielded supramolecular elastomers with acovalently cross-linked phase induced by UV irradiation combined witha noncovalent UPy cross-linked phase induced by secondary hydrogenbonding interactions. Of particular note, it was determined that thepresence of UPy hydrogen-bonded aggregates accelerated the UV cross-linkingprocess during the initial stage of exposure. This observation wasattributed to microphase-separated structure of UV-irradiated supramolecularelastomer, where UPy aggregation increased the probability of interactionbetween the pendant vinyls responsible for UV cross-linking. The systematicstudy of uniaxial tensile behavior of the UV-irradiated supramolecularelastomers offers new insight into the design and architecture ofmechanically tunable supramolecular elastomers. [ABSTRACT FROM AUTHOR]

ABSTRACT In this article, we introduce a new method for preparing ultrasmall chitosan (CS)/succinyl β-cyclodextrin (SCD) nanoparticles (NPs) intended for loading bovine serum albumin (BSA) as a model protein. The proposed method is based on the complex coacervation technique followed by ionotropic gelation with tripolyphosphate. SCD, an anionic derivative of cyclodextrin, was synthesized and used in CS-based NPs to enhance the entrapment efficiency of BSA. The results show that with this approach, ultrasmall, compact, and neutralized NPs with a mean particle size near 30 nm were obtained. A high degree of protein entrapment in the NPs led to a significant improvement in the BSA release profile with a low initial burst release (ca. 3% w/v of the initially loaded BSA) and a sustained release over time. This enabled a suitable nanocarrier for long-term protein delivery (30% release over 120 h). © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 39648. [ABSTRACT FROM AUTHOR]

A systematic study was done on morphological, electrical and rheological behavior of co-continuous or dispersed-type polycarbonate (PC)/acrylonitrile-styrene-butadiene (ABS) blends, containing different amounts of multiwalled carbon nanotubes (MWNT). The MWNTs gave substantial electrical conductivities to these nanocomposites at very low concentrations, owing to the effective melt processing method. Because of selective localization of MWNTs in the PC phase, along with double percolation phenomenon, the blend with co-continuous morphology showed a lower electrical and rheological percolation threshold, higher melt viscosity and elasticity, as compared to the system with dispersed morphology. The morphology of both the blend systems was refined as a result of MWNTs incorporation but the morphology type remained unchanged. A typical role of compatibilizer in refining blend morphology was observed in both the systems. The electrical conductivity of the system filled with MWNTs in presence of compatibilizer, was lower than the systems filled with MWNTs only, which was attributed to role of compatibilizer in directing a part of MWNTs from PC matrix toward ABS phase. With increasing compatibilizer/MWNTs ratio, the influence of compatibilizer on morphology refinement and conductivity reduction was intensified. By comparing TEM micrograph of PC/SAN/MWNTs with that of PC/ABS/MWNTs, it was revealed that small portion of MWNTs was also located on polybutadiene rubber fraction of ABS. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 739-748, 2013 [ABSTRACT FROM AUTHOR]

Biomimetic, stimuli-responsive polymer nanocomposites based on a hydrophobic styrene-butadiene rubber (SBR) matrix and rigid, rod-like cellulose nanocrystals (CNCs) isolated from cotton were prepared by three different approaches, and their properties were studied and related to the composition, processing history, and exposure to water as a stimulus. The first processing approach involved mixing an aqueous SBR latex with aqueous CNC dispersions, and films were subsequently formed by solution-casting. The second method utilized the first protocol, but films were additionally compression-molded. The third method involved the formation of a CNC organogel via a solvent exchange with acetone, followed by infusing this gel, in which the CNCs form a percolating network with solutions of SBR in tetrahydrofuran. The thermomechanical properties of the materials were established by dynamic mechanical thermal analysis (DMTA). In the dry state, all nanocomposites show much higher tensile storage moduli, E', than the neat SBR or the SBR latex. E' increases with the CNC content and depends strongly on the processing method, which appears to influence the morphology of the SBR nanocomposites produced. The highest E' values were observed for the solution cast samples involving an SBR latex, where E' increased from 3 MPa for the neat SBR to ca. 740 MPa for the nanocomposite containing 20% v/v CNCs. Upon submersion in deionized water, a dramatic reduction of E' was observed, for example from 740 to 5 MPa for the solution-cast nanocomposite containing 20% v/v CNCs. This change is interpreted as a disengagement of the percolating CNC network, on account of modest aqueous swelling and competitive hydrogen bonding of water molecules with the CNCs. It is shown that the method of preparation also influenced the swelling behavior and kinetics of modulus switching, consistent with different arrangements of the CNCs, which serve as channels for water absorption and transport within the hydrophobic SBR matrix.