Ternary nanocomposites based on poly(butylene terephthalate) (PBT), maleic anhydride grafted poly(ethylene‐co‐vinyl acetate) (EVA‐g‐MAH), and organically modified montmorllonite (organoclays) were prepared through four different blending sequences in a Haake rheocord mixer: (1) To blend PBT, EVA‐g‐MAH and organoclays in one step; (2) First to prepare EVA‐g‐MAH/organoclay nanocomposite, then mix it with PBT to get the final nanocomposite; (3) To mix PBT with organoclays first, then the PBT/organoclay nanocomposite with EVA‐g‐MAH. (4) To mix organoclays with the PBT/EVA‐g‐MAH blend. The microstructure of the PBT/EVA‐g‐MAH/organoclay ternary hybrids was characterized by X‐ray diffraction (XRD) and transmission electron microscopy (TEM). It was found that the blending sequence significantly influences the microstructure of PBT/EVA‐g‐MAH/organoclay ternary hybrids and the dispersion behavior of the organoclays in the polymer matrix. Tensile and impact properties of the hybrids were also studied. The results showed that the mixing sequence (2) gives the best tensile and impact strength due to its fine “sea‐island” morphology of PBT/EVA‐g‐MAH blend and good dispersion of the organoclays in the continuous PBT matrix.

Boronic acid-based sensors for saccharides have been developed via biocatalysis. The self-doped copolymer of poly(aniline-co-3-aminobenzeneboronic acid) [poly(aniline-co-AB)], with various mole ratios of two components, was synthesized by oxidative enzymatic polymerization using a natural biocatalyst such as horseradish peroxidase together with an anionic polyelectrolyte template (sulfonated polystyrene) under mild conditions (pH 4.5). Poly(aniline-co-AB), having an aniline boronic acid-to-aniline ratio of 1:2 on average, gave rise to a green doped polymer with absorption maxima at 745 nm. The potentiometric detection of saccharides using poly(aniline-co-AB) is presented. Characteristics of both transient and steady-state response associated with the complex formation of poly(aniline-co-AB) with various saccharides were monitored by UV-vis spectroscopy and cyclic voltammetry (CV). The results obtained from UV-vis spectroscopy and CV show that the sensitivity of enzymatically synthesized water-soluble poly(aniline-co-AB) for various saccharides was improved significantly compared to the chemically synthesized counterpart. A possible mechanism for the sensitive detection of sugar molecules by boronic acid is proposed on the basis of UV-vis and IR spectrophotometry, and four-point probe conductivity measurements.

ABSTRACT:A new type of polyimide/silica (PI/SiO 2 ) hybrid composite films was prepared by blending polymermodified colloidal silica with the semiflexible polyimide. Polyimide was solution-imidized at higher temperature than the glass transition temperature (T g ) using 3,3Ј,4,4Ј-biphenyltetracarboxylic dianhydride (BPDA) and 4,4Ј-diaminodiphenyl ether (ODA). The morphological observation on the prepared hybrid films by scanning electron microscopy (SEM) pointed to the existence of miscible organicinorganic phase, which resulted in improved mechanical properties compared with pure PI. The incorporation of the silica structures in the PI matrix also increased both T g and thermal stability of the resulting films.

A synthesized water‐dispersible graft copolymer (WDGP) was evaluated as a coupling agent in carbon fiber/isotactic polypropylene composites. Measurements of the interfacial shear strength (IFSS) were made using single fiber composite (SFC) specimens. A graft copolymer of isotactic polypropylene backbone grafted with polyacrylamide (PAAm) was synthesized for testing as a coupling agent. Optimal conditions for the coupling agent treatment and SFC specimens preparation were established. Improvement in the IFSS was 18% at room temperature, whereas improvement was >60% under wet conditions, after 1 h in boiling water. This improvement is due to chemical bonding in the interphase between functional groups in carbon fiber and PAAm in WDGP coupling agent, and interdiffusion in the interphase between IPP in WDGP coupling agent and matrix IPP. The hydrophobic nature of the interfacial region and crosslinking between amide groups in grafted PAAm chains based on inter‐ and intramolecular interactions may be the reason for the high improvement of the IFSS under wet conditions. In addition, the spherulite size and transcrystallinity seem to correlate with the IFSS of SFC specimens.

Three structurally different aniline monomers, which can not be polymerized by chemical methods, have been polymerized with horseradish peroxidase. Enzymatic synthesis of linear polyaniline requires template molecules to minimize branching in the polyaniline backbone. Monomers having methoxy and methyl blocking groups at the ortho or meta position could induce the conducting form of para-linked polyaniline without the use of an anionic template, such as SPS. A new mild peroxide, peroxyacetic acid, was identified and used to oxidize horseradish peroxidase in water.