Textile‐surface interfacial asymmetric polymerization

This research demonstrated that polymerization of aniline on cellulose produces chiroptically active composites. Polymerization of aniline in the presence of cotton fibers consisting of chiral cellulose are performed to prepare a polyaniline (PANI)/cotton composite. The polymerization is conducted at the cotton interface. The resultant PANI/cotton composite shows chiroptical activity elucidated with diffuse reflectance circular dichroism. In this reaction, textile‐surface interfacial asymmetric polymerization is performed with imprinting of chiral structure from the cotton as a natural chiroptically active polymer to the PANI. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41118.     

Terpolymers as precursors for CuO nanoparticles synthesis

This work describes the synthesis of terpolymers of aniline, diphenylamine, and o‐anthranilic acid (PANIDPAA) by 1 : 1 : 1 molar ratio of the respective monomers doped by different concentration of copper ions via in situ chemical terpolymerization. The results are justified by measuring spectral characteristics namely, UV‐vis absorption spectra, FTIR, and TGA. Calcining these PANIDPAA terpolymers doped by copper at temperatures in the range of 700°C led to the formation of CuO nanoparticles in the nanoscale by thermal decomposition in air directly. The stages of decompositions and the calcination temperature of the precursors have been determined from thermal analysis data sheet. The obtained CuO nanoparticles have been characterized by X‐ray diffraction and transmission electron microscope (TEM). TEM showed a particle size less than 40 nm. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41150.     

Self‐welding 1‐butene/ethylene copolymers from metallocene catalysts: Structure,morphology, and mechanical properties

Samples of random copolymers consisting of 1‐butene modified with a low ethylene content (4, 5, 8% by weight) produced with metallocene catalysts were studied to elucidate the polymorphic behavior of this new class of materials and to characterize them from a structural, morphological, and mechanical point of view. The samples cooled down from the melt are in amorphous phase and crystallize in a mixture of form I and I′ or in pure form I′ with aging time, according to the C2 content. Infrared and nuclear magnetic resonance spectroscopy, X‐ray diffraction and microscopic techniques were used to follow the changes of the material with aging time and to correlate the structural and morphological behavior with the peculiar mechanical properties that differentiate the samples with increasing C2 content. The presence, in the aged samples with higher C2 content, of the pure form I′ induces the peculiar ability to self‐welding and these copolymers combine high flexibility with good elasticity and ductility and can be processed directly or used as modifying agents in polymers. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40119.     

Nanopaper membranes from chitin–protein composite nanofibers—structure and mechanical properties

Chitin nanofibers may be of interest as a component for nanocomposites. Composite nanofibers are therefore isolated from crab shells in order to characterize structure and analyze property potential. The mechanical properties of the porous nanopaper structures are much superior to regenerated chitin membranes. The nanofiber filtration‐processing route is much more environmentally friendly than for regenerated chitin. Minerals and extractives are removed using HCl and ethanol, respectively, followed by mild NaOH treatment and mechanical homogenization to maintain chitin–protein structure in the nanofibers produced. Atomic force microscope (AFM) and scanning transmission electron microscope (STEM) reveal the structure of chitin–protein composite nanofibers. The presence of protein is confirmed by colorimetric method. Porous nanopaper membranes are prepared by simple filtration in such a way that different nanofiber volume fractions are obtained: 43%, 52%, 68%, and 78%. Moisture sorption isotherms, structural properties, and mechanical properties of membranes are measured and analyzed. The current material is environmentally friendly, the techniques employed for both individualization and membrane preparation are simple and green, and the results are of interest for development of nanomaterials and biocomposites. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40121.     

Improved zein films using polyethylenemaleic anhydride

The effect on the physical properties and solubility of corn protein (zein) films was studied after reaction of zein with polyethylenemaleic anhydride (PEMA). Reactions were carried out in dimethylformamide (DMF) solution where the concentration of PEMA was varied between 0 and 6%. After reaction at room temperature, cast films were prepared, and the physical and solubility properties were determined. Incorporating more than 2% PEMA provided films with increased tensile strength and elongation. Incorporating 6% PEMA provided films with higher tensile strength (32–42 MPa) and improved solvent resistance (100–21% solubility) relative to control. If the films were heated in an oven, the film's solubility decreased further. Solution rheology experiments demonstrated that the zein and PEMA formed a cross‐linked gel with time in DMF. Dynamic mechanical analysis experiments have shown that the PEMA‐modified zein films undergo a dramatic loss in modulus on reaching 116°C, whereas the control experiences this loss at 98°C. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40122.     

Cotton fibers reinforcement of HNBR: Control of fiber alignment and its influence on properties of HNBR vulcanizates

This article focuses on the reinforcement of hydrogenated acrylonitrile butadiene rubber (HNBR) by cotton fiber as natural reinforcing filler. The effect of fiber alignment on the properties of HNBR compounds and vulcanizates is investigated. Properties of interest include rheological behavior, cure, tensile, abrasion, and dynamic mechanical properties which are correlated to the magnitudes of state‐of‐mix, bound rubber content, crosslink density and fiber alignment. Results obtained reveal that mechanical properties of rubber composites are improved dramatically by the addition of cotton fiber due to the enhanced hydrodynamic effect in association with crosslink density. Furthermore, the degree of fiber alignment is found to depend strongly on shear strain. The results demonstrate the importance of fiber alignment controlled efficiently by shear strain. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41090.     

Influence of the processing parameters and composition on the thermal stability of PLA/nanoclay bio‐nanocomposites

Poly(lactic acid) (PLA) is one the most promising bio‐based and biodegradable polymer. However, its low thermal stability limits the range of applications and complicates its transformation via the most industrial common processes. The novelty of this work is studying the thermal stability of PLA and PLA/clay nanocomposites during use, as a function of the composition and using a wide range of extrusion and injection moulding processing parameters. To improve the thermal stability of the PLA, laminar silicates containing different organomodifications have been added (Cloisite 20A and Cloisite 30B). The results show that the processing conditions and composition define the morphology of the bio‐nanocomposites, which plays key role in defining final thermal properties of the material. In general, clays improve the thermal stability of the processed material, increasing the degradation temperature and decreasing the degradation rate under a wide range of processing conditions. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40747.     

Nonsalt 1‐(arylmethyloxy)pyrene photoinitiators capable of initiating cationic polymerization

Analysis of photoproducts derived from 1‐(methoxynaphthalen‐1‐ylmethyloxy)pyrene initiators and polymer end groups demonstrated that methoxynaphthalen‐1‐ylmethyl carbocation is involved in the initiation steps for both styrene (St) and cyclohexene oxide (CHO) polymerization. Charge transfer from the pyrenyloxy oxygen atom to the methoxynaphthalen‐1‐ylmethyl chromophore in the singlet excited state is assumed to be responsible for the efficient generation of the carbocation species, which also initiates the copolymerization of St and CHO. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40510.     

Design of XNBR nanocomposites for underwater acoustic sensor applications: Effect of MWNT on dynamic mechanical properties and morphology

In this work, application of rubber‐MWNT nanocomposite for underwater acoustic sensors is explored. The nanocomposite is developed by incorporating multiwalled carbon nanotubes (MWNT) into carboxylated nitrile rubber by mechanical mixing. The addition of MWNT up to 10 phr is found to result in about 330% increase in tensile strength, 140% increase in modulus, and 160% increase in tear strength. Transmission electron microscopy and scanning electron microscopy analyses indicate uniform dispersion of nanotubes in the rubber matrix. Dynamic mechanical analysis shows that damping at ambient temperature gradually increases with increasing filler content. This is attributed to the augmented frictional energy loss at the interface. The damping peak position shifts upward with increase in MWNT concentration, which may be gainfully used to tune to the operational frequency range of underwater acoustic sensors. Payne effect is observed at higher filler concentration due to the breakage of aggregates formed by filler–filler interaction. The nanocomposite may find application for damping structural vibrations and thus to improve the performance of underwater acoustic sensors. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40752.     

Developing toughened aromatic polybenzoxazines using thermoplastic oligomers and telechelics,part 1: Preparation and characterization of the functionalized oligomers

The preparation and characterization of three families of thermoplastic oligomers (M_n = 2918–13263 g mol^?1) based on polyarylsulfone (PSU) differing in both molecular weight and terminal functionality and one series of polyarylethersulfone (PES) of different molecular weights is reported. Infrared and nuclear magnetic resonance spectroscopy data support the formation of both the hydroxyl terminated oligomers and conversion (67–89% depending on molecular weight) to the telechelic PSU oligomer bearing reactive benzoxazine groups. Differential scanning calorimetry reveals that the onset of homopolymerization in the telechelic PSU oligomer occurs at around 100°C (peak maximum 125°C at 10 K/min) and rescans show values of the glass transition (for the homopolymers) ranging from 124 to 167°C depending on molecular weight. The influence on the oligomer backbone and terminal functionality is examined using thermal analysis. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40875.