Digestion of crosslinked poly(vinylpyridinium halide) by activated sludge,and application to make poly(methyl methacrylate) biodegradable by incorporation of a pyridinium group into the main chain

Crosslinked poly(N-benzyl-4-vinyipyridinium bromide) has been found to be digested by activated sludge obtained from sewage works. As an extension of this work, the authors attempted to make poly(methyl methacrylate) biodegradable by incorporation of a pyridinium group. Poly(methyl methacrylate) containing a small amount of N-benzyl-4-vinylpyridinium chloride in the main chain showed remarkable reduction in molecular weight and gravimetric weight when placed in an aeration tank of a sewage works. Molecular weight reduction by activated sludge was more conspicuous when content of the pyridinium group was larger and the original molecular weight before the biological treatment was lower. Since insoluble pyridinium-type polymer captures microbial cells alive, this biodegradation appears to be facilitated by enhancement of affinity of the synthetic hydrophobic polymer with cells of microogranisms. © 1994 John Wiley & Sons, Inc.     

An improved prediction result of entropic‐FV model for vapor–liquid equilibria of solvent–polymer systems

In this work, entropic expressions of UNIFAC‐FV and Entropic‐FV models were evaluated by using an extensive database of infinite dilution vapor–liquid equilibrium (VLE) data of athermal systems containing polypropylene, polyethylene, and polyisobutylene. For the infinite dilution athermal systems, performance of the Entropic‐FV model was better than that of the UNIFAC‐FV model. Then, finite concentration VLE data of non‐athermal systems that consisted of 16 polymers and 36 solvents containing a large variety of solvent–polymer systems ranging from nonpolar to polar substances were considered to optimized 46 pairs of group interaction parameters of the Entropic‐FV model. For systems containing polar solvents of three types of solvents studied, revised group interaction parameters gave significant improvements from 17.9 to 13.0% average absolute deviation (AAD) of solvent activities. For overall results, improvements were achieved from 15.1 to 12.4% AAD. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 1145–1153, 2005     

Silica films with a single-crystalline mesoporous structure

Films of mesoporous materials attract broad interest because of their wide applicability in the fields of optics and electronics. Although many of these films have a regular local porous structure, the structural regularity has not been used practically yet because of difficulties in its control on macroscopic scales. Here, we demonstrate the preparation of mesoporous silica films whose porous structure can be described as a single crystal, that is, a long-range order of cage-like pores is maintained over centimetre scales. These films have a three-dimensional hexagonal (space group P6(3)/mmc) porous structure, and the in-plane arrangement of the pores is strictly controlled by a polymeric substrate surface that has been treated by rubbing. This new class of single-crystalline films with mesoscopic periodic structure is a significant breakthrough in bottom-up nanotechnology, and could lead to novel devices, for example, optics in a soft X-ray region, and quantum electronics.     

Effect of off-orientation of seed crystal on silicon carbide (SiC) single-crystal growth on the (11 $$\bar 2$$ 0) surface0) surface

The effect of off-orientation growth has been investigated in terms of stacking fault formation during physical vapor transport (PVT) growth of silicon carbide (SiC) single crystals on the (11 0) seed crystal surface. Occurrence of stacking fault formation is largely dependent on the direction of off-orientation, and basal plane stacking fault density is significantly reduced by growing the crystals on a (11 0) seed crystal off-oriented toward 〈0001〉. The density of the basal plane stacking faults rapidly decreases from 100–150 cm⁻¹ to ∼10 cm⁻¹ as the degree of off-orientation is increased from 0 to 10 deg. The results are interpreted in the framework of microscopic facet formation during PVT growth, and the introduction of off-orientation of seed crystal is assumed to prevent (01 0) and (10 0) microfacet formation on the (11 0) growing surface through modification of the surface growth kinetics and to suppress the stacking fault formation. An erratum to this article is available at .     

Synthesis of Nanohole‐Structured Single‐Crystalline Platinum Nanosheets Using Surfactant‐Liquid‐Crystals and their Electrochemical Characterization

Nanohole‐structured single‐crystalline Pt nanosheets have been synthesized by the borohydride reduction of Na₂PtCl₆ confined to the lyotropic liquid crystals (LLCs) of polyoxyethylene (20) sorbitan monooleate (Tween 80) with or without nonaethylene‐glycol (C₁₂EO₉). The Pt nanosheets of around 4–10 nm in central thickness and up to 500 nm or above in diameter have a number of hexagonal‐shaped nanoholes ∼1.8 nm wide. High‐resolution electron microscope images of the nanosheets showed atomic fringes with a spacing of 0.22 nm indicating that the nanosheets are crystallographically continuous through the nanoholed and non‐holed areas. The inner‐angle distributions for the hexagonal nanoholes indicate that the six sides of the nanoholes are walled with each two Pt (111), Pt (1 1) and Pt (010) planes. The formation mechanism of nanoholed Pt nanosheets is discussed on the basis of structural and compositional data for the resulting solids and their precursory LLCs, with the aid of similar nanohole growth observed for a Tween 80 free but oleic acid‐incorporated system. It is also demonstrated that the nanoholed Pt nanostructures loaded on carbon exhibit fairly high electrocatalytic activity for oxygen reduction reaction and a high performance as a cathode material for polymer‐electrolyte fuel cells, along with their extremely high thermostability revealed through the effect of electron‐irradiation.     

Solubility of propylene in semicrystalline polypropylene

Gas solubilities and polymer swelling in propylene and semicrystalline polypropylene system at temperatures of 323.2 and 348.2 K and pressures up to propylene's vapor pressure were measured. Pressure, specific volume, and temperature (PVT) measurements of polypropylene were carried out at temperatures from 313 to 573 K and pressures up 200 MPa. Two kinds of polypropylenes, which had different stereoregularities, were used for both solubility and PVT measurements. The solubilities were correlated with the Sanchez–Lacombe equation of state (EOS) with temperature‐dependent binary interaction parameters to within 5% average relative percentage deviation. Swelling ratios estimated with Sanchez–Lacombe EOS coupled with optimized interaction parameters were 20% lower than the experimental values. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 79: 1134–1143, 2001     

Carbon-supported growth of cross-linked platinum nanowires by surfactant templating and their elecrochemical characterization

Platinum/carbon (Pt/C) composite materials were prepared by the hydrazine reduction of H2PtCl6 confined to a mixed surfactant lytropic liquid crystal (LC)/C mixture with varying amounts of water. The reaction at relatively low water contents successfully yielded cross-linked Pt nanowires with wire-widths of 2-5 nm. The novel Pt nanostructure is believed to be from poorly hydrated hexagonal domains formed together with layered domains by the phase separation of the precursory LC mixture in the presence of carbon. Electrochemical measurements using cyclic volutammetry and membrane electrode assemblies revealed that the cross-linked nanowired Pt/C composite exhibits fairly high electrocatalytic activity for oxygen reduction reaction, as well as a high performance as the cathode material for polymer electrolyte fuel cells.     

Accumulative gene integration into a pre-determined site using Cre/loxP

Site-specific gene recombination systems, such as Cre/loxP, have been used for genetic modification of cells and organisms in both basic and applied research. We previously developed an accumulative gene integration system (AGIS), in which target gene cassettes could be repeatedly integrated into a pre-determined site on a plasmid or cellular genome by recombinase-mediated cassette exchange (RMCE), using Cre and mutated loxPs. In the present study, we designed a simplified AGIS. For gene integration into a target site, the previous system used two loxP sites in the acceptor DNA, whereas the new system uses a single loxP site. The gene integration reactions were repeated four times in vitro using Cre protein and specific plasmids. The expected integration reactions mediated by Cre occurred at the loxP sites, resulting in integration of four target genes. The system was also used for genomic integration of reporter genes using Chinese hamster ovary (CHO) cells. The reporter genes were efficiently introduced into the CHO genome in a Cre-dependent manner, and transgene expression was detected after the integration reaction. The expression levels of the reporter genes were enhanced, corresponding to the increase of transgene copy number. Recombinase-mediated AGIS provides a useful tool for the modification of cellular genomes.     

Solubility of butane and isobutane in molten polypropylene and polystyrene

The solubility of butane and isobutane in molten polypropylene (PP) and polystyrene (PS) was measured at pressures up to 3 MPa and along four isotherms from 438 to 483 K for PP and from 348 to 473 K for PS. The solubility increased with increasing pressure and decreasing temperature. At 438 K and 2 MPa, the solubilities of butane and isobutane in PP were 0.15 and 0.11 g‐gas/g‐polym, respectively. At 423 K and 2 MPa, the solubilities of butane and isobutane in PS were 0.08 and 0.05 g‐gas/g‐polym, respectively. Solubility could be correlated with the Sanchez‐Lacombe equation of state with temperature‐dependent binary interaction parameters to within 4.4% average relative deviation. Henry's constant for these gases in the PP and PS obtained in this work were used to determine correlation equations along with literature data. Polym. Eng. Sci. 44:2083–2089, 2004. © 2004 Society of Plastics Engineers.