ABSTRACTA facile strategy for the synthesis of polystyrene/Fe3O4 nanocomposite is suggested. For this purpose, styrene and 4-chloromethyl styrene monomers was copolymerized through reversible addition of fragmentation chain transfer technique [P(St-co-CMSt)] and then the chlorine groups of CMSt units were converted to diethyl malonate groups through a nucleophilic substitution reaction. Afterward, esteric groups of diethyl malonate were hydrolyzed to afford carboxylic acid-functionalized polystyrene. This polymer with carboxylic acid groups can adsorbed onto the surface of Fe3O4 nanoparticles through the interaction with hydroxyl groups onto the surface of the nanoparticles. We envision that the synthesized PSt/Fe3O4 nanocomposite may be find applications in electromagnetic interference shielding and environment sciences.

ABSTRACTPhysical/chemical interaction in blends of high-density polyethylene with polyamide 6 and polyethylene-co-vinyl alcohol compatibilized with maleic anhydride-grafted high-density polyethylene was discussed. The performance of maleic anhydride-grafted high-density polyethylene was assessed by domain size variation and interfacial adhesion examination. Analysis of impact strength elucidated physical interaction improvement by compatibilization (entanglements and hydrogen bonding), while chemical reactions between ‒OH and ‒NH (from polyethylene-co-vinyl alcohol and polyamide 6, respectively) and ‒COOH functional groups resulting from ring-opening of maleic anhydride determined interfacial adhesion reinforcement, where interfacial adhesion parameter changed from 0.75 for noncompatibilized to 0.96 compatibilized high-density polyethylene/polyamide 6, but remained unchanged for high-density polyethylene/polyethylene-co-vinyl alcohol blends, from 0.98 to 1.02.

ABSTRACTA homogenous binary metallocene catalytic system comprising of isospecific rac-Me2Si(2-Me-4-Ph In)2ZrCl2(I) producing high molecular weight isotactic polypropylene and oscillating (2-Ph In)2ZrCl2(II) precursor producing low isotactic elastomer polypropylene at three varying molar ratios of two types of catalysts was used to synthesize polypropylene reactor blends. Dynamic mechanical thermal analysis and rheological properties along with molecular weight of synthesized polypropylene reactor blends were studied and correlations among these properties were established. It was found that molar ratio of catalysts is a significant factor in determination of molecular weight and its distribution. The produced polymers with unimodal molecular weight distribution showed intermediate modulus during dynamic mechanical thermal experiment, while the ones with bimodal molecular weight distribution exhibited a kind of phase separation at low temperature. Depending on strength of the developed structures, determined by the presence of interfacial connectors, the modulus could be adjusted. Origins of other types of relaxations and their differences for each type of the developed products were discussed in detail. From rheological results and particularly the relaxation curves, the characteristics of the chain structure of the synthesized reactor blends could be resolved. It was revealed that one of the synthesized polymers had long chain branches unlike the rest of the samples having linear chain structure.

ABSTRACTThe presence of nanosized clay fillers can greatly influence the crystallization behaviors and crystalline morphologies of polymer composites. In this study, the modified montmorillonite polyethylene nanocomposites have been prepared by melt mixing, followed by injection molding. The morphology and microstructure of the composites were characterized by scanning electron microscopy and Fourier transform infrared spectrometry. The nanosized clay particles act as a nucleating agent in the solidification process of the matrix. The relative crystallinity ratio decreases with the decrement of polymer loading. Nonisothermal and isothermal crystallizations were conducted to characterize the crystallization kinetics of nanocomposites. The effects of clay dispersion on the crystallization of polymer were quantified by Avrami and Hoffman models. The addition of 1 wt% clay into polymer matrix has significantly increased the activation energy. The crystallization rate constants (G) have been determined which are higher for the composites than that for the polymer matrix.

ABSTRACTPolymeric ionic liquids or poly(ionic liquid)s combine unique properties of ionic liquids with macromolecular characteristics. One of the spotlights of review was to identify potential areas of poly(ionic liquid)s. Due to unique combination of polymer and counterions, poly(ionic liquid)s possess tunable properties to be employed in range of advanced applications. Poly(ionic liquid)s composites have claimed relevance in energy storage/production and catalysis. In biosensors, poly(ionic liquid)s were employed to fabricate enzyme electrodes. Moreover, stimuli-responsive copolymers were used to form multi-responsive poly(ionic liquid)s. Separation membranes have been reported for gas separation/storage/transport. A significant use of poly(ionic liquid)s was found as solid-state electrolyte. In fuel cell, poly(ionic liquid)s-based electrolyte membranes were employed.

ABSTRACTThe current study discusses the synthesis of novel gelatin–chitosan lactate cohydrogels. Mechanical studies indicated the viscoelastic nature of the cohydrogels. The cohydrogels were predominantly elastic in nature. Inherent mechanical stability of the cohydrogels was better than the pristine gelatin hydrogel. Incorporation of chitosan lactate improved the in vitro swelling and the drug release properties of the cohydrogels. The cohydrogels showed good antimicrobial drug delivery capacity. The properties of the developed cohydrogels demonstrated that they could be used as delivery vehicles for antimicrobial drugs. Cell proliferation study suggested that the cohydrogels supported the proliferation of the human keratinocytes.

ABSTRACTThis review exclusively addresses material systems primarily based on poly(vinyl alcohol) (PVA), one of the most popular water-soluble biopolymers, for their use in packaging applications with the primary objective of reducing petrobased plastic waste. In addition, some typical PVA blends and nanocomposites are discussed as comparative studies for material packaging. Structural characteristics, mechanical, thermal, and barrier properties, in addition to biodegradation of these multiple material systems are summarized in a systematic manner. Finally, associated fabrication processing methods together with the most popular theoretical models used for the permeability of PVA nanocomposites are also reviewed in detail.

ABSTRACTThis study used poly(butylene succinate) and poly(ethylene glycol) to modify poly(3-hydroxybutyrate-co-3-hydroxyvalerate). The results showed that the incorporation of poly(butylene succinate) and poly(ethylene glycol) improved the mechanical properties of blends. The results showed that crystallinity of the poly(ethylene glycol)-containing blends decreased, so do the crystallization temperature and melting temperature of the poly(3-hydroxybutyrate-co-3-hydroxyvalerate) component of blends. Poly(butylene succinate)/poly(3-hydroxybutyrate-co-3-hydroxyvalerate)/poly(ethylene glycol) ratio of 50:20:30 was chosen owing to its good properties. The poly(3-hydroxybutyrate-co-3-hydroxyvalerate) component of blends can be degraded completely by Pseudomonas mendocina DS04-T, whereas this strain cannot degrade poly(butylene succinate) and poly(ethylene glycol). Apart from poly(butylene succinate), Fusarium sp. FS1301 can also biodegrade poly(3-hydroxybutyrate-co-3-hydroxyvalerate) and poly(ethylene glycol).

ABSTRACTNew poly(amide-imide)/amino functionalized Fe3O4 nanocomposites were successfully fabricated through solution intercalation technique. A poly(amide-imide) derived from an imide-containing diacid and ether linkage diamine was synthesized and characterized. Aiming to have better compatibility, the hydrophilic nature of Fe3O4@SiO2 was changed into organophilic using N-[3-(trimethoxysilyl)propyl]ethylenediamine. The amino-functionalized Fe3O4 showed well dispersion in the poly(amide-imide) matrix. Thermal gravimetric analysis results indicated that char yields of the nanocomposites were improved. Microscale combustion calorimetry results showed that poly(amide-imide) had good flame retardancy and amino-functionalized Fe3O4 has further improved this property of poly(amide-imide).

ABSTRACTBulk heterojunction blend of poly(3-hexylthiophene)–[6,6]-phenyl-C61-butyric acid methyl ester prepared using the ternary solvent mixture was used as the active layer of an inverted organic solar cell. The ternary solvent mixture consisted of a good solvent such as ortho-dichlorobenzene and two marginal solvents such as cyclohexanone and toluene offering limited solubility to the poly(3-hexylthiophene) component. Power conversion efficiency of inverted device was found to decrease from 2.74 ± 0.05% in the unmodified device to 2.64 ± 0.07% in the modified device. UV–visible measurement revealed less efficient photoabsorption in the mixed cosolvent-casted active layer due to insufficient and disordered crystallization of poly(3-hexylthiophene) domains.