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  • Polymer and Materials Science  (206)
  • 1995-1999  (205)
  • 1955-1959  (1)
  • 11
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 6 (1995), S. 42-46 
    ISSN: 1042-7147
    Keywords: PPLC ; phenoxy ; electrooptic property ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Morphology and electro-optic properties of composite films composed of phenoxy and nematic liquid crystal (LC) have been studied at a film composition of 40/60 (polymer/LC by weight). Effects of temperature, frequency and voltage of applied a. c. electric field on the transmittance and response time of the films were measured.
    Additional Material: 8 Ill.
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 59 (1996), S. 1639-1649 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A series of the blends of tetrafunctional epoxy resins with polycarbonate (PC) or tetramethyl polycarbonate (TMPC) was prepared to investigate thermal stability and compatibility. The Tg behavior as a function of isothermal curing time was observed. The thermal stability of epoxy and epoxy/thermoplastics blends was estimated using thermogravimetric analysis (TGA). Fourier transform infrared (FTIR) investigation demonstrated the occurrence of thermal degradation and hydrolysis in epoxy and epoxy/PC blends during the curing process. The thermal degradation of cured epoxy was induced with etherification, a sort of side reaction, and resulted in the chain scission of networks leading to the decrease of Tg. The variance of thermal stability with a combination of two components in these blends resulted from the difference of the compatibility due to chemical structure similarity. The compatibility was corroborated with the morphology by scanning electron microscopy (SEM). © 1996 John Wiley & Sons, Inc.
    Additional Material: 18 Ill.
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  • 13
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 625-636 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Polypyrrole (PPY) films having high conductivity were synthesized electrochemically in acetonitrile at low temperature and low current density. Pristine, deprotonated, and ozone-pretreated PPY films were subjected to either thermally induced or near-UV-light-induced graft copolymerization with acrylic acid (AAc), or sodium salt of 4-styrenesulfonic acid (NaSS). Surface structures and redox states of the pristine, deprotonated, reprotonated, and surface-modified polypyrrole films were studied by angle-dependent X-ray photoelectron spectroscopy (XPS). The morphology of the PPY surface after modification by graft co-polymerization was revealed by atomic force microscopy (AFM). The results showed that the density of surface grafting decreased with ozone pretreatment. Surface grafting of the two polymeric acids also gave rise to a self-protonated surface structure. A substantial proportion of the grafted protonic acid groups at the surface remained free for further surface functionalization. The surface characteristics, in particular the charge-transfer interactions and the changes in the intrinsic redox states of the substrate films, associated with the external protonation and surface self-protonation processes were also discussed. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 14
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1011-1021 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: UV-curable polyurethane acrylates for poly(vinyl chloride) (PVC) floor coating were prepared using nonyellowing polyisocyanates. The effects of the chemical structure of the polyisocyanates and hydroxyacrylates, and the compositions of the prepolymer/diluent on the properties of the UV-curable polyurethane acrylates were investigated. Several different urethane acrylate prepolymers from four different polyisocyanates, isophorone diisocyanate (IPDI) adduct, hexamethylene diisocyanate (HDI) adduct, HDI biuret, and HDI isocyanurate, and two different hydroxyacrylates, hydroxyapropyl acrylate (HPA), polycaprolactone modified hydroxyethylhexylacrylate (PCMHEA). UV-curable coating materials were formulated from the prepolymers and 1-hydroxycyclohexylphenyl ketone as a photoinitiator with polyethylene glycol diacrylate (PEGDA) as a diluent. The polyurethane acrylates prepared with HDI isocyanurate and the equimolar mixture of HPA and PCMHEA showed balanced coating properties such as tensile properties, hardness, weatherability, and good adhesion. The dynamic mechanical studies showed the properties of those polyurethane acrylates were well correlated with their glass transition temperature behaviors. It was also found that the adhesion was best as a PVC floor coating with the appropriate viscosity (below 150 P at 25°C) when 35% PEGDA as a diluent was used. © 1996 John Wiley & Sons, Inc.
    Additional Material: 17 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 57 (1995), S. 1347-1358 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Nylon 6 was prepared by adiabatic anionic polymerization of ∊-caprolactam using hexamethylene dicarbamoyl dicaprolactam (HDC), cyclohexyl carbamoyl caprolactam (CCC), or phenyl carbamoyl caprolactam (PCC) as activators and sodium caprolactamate (NaCL) as a catalyst at various initial reaction temperatures ranging from 130 to 160°C. Adiabatic temperature rise was recorded as a function of polymerization time to investigate polymerization kinetics. Kinetic parameters for polymerization, which are more accurate than data reported to date, could be obtained by fitting the temperature rise data with a new polymerization kinetic equation involving crystallization exotherm and thermal conduction. The polymerization rate highly depended on the chemical structure of the activator used, which indicates that the initiating step where the activator is attacked nucleophilically by NaCL is a very important reaction step, affecting the overall polymerization rate. CCC showed the fastest polymerization rate, whereas HDC and PCC showed the medium and the slowest rate, respectively. The contributions of crystallization exotherm and thermal conduction to the resultant temperature rise during polymerization were significant, when the initial reaction temperature was lower than 140°C. In all cases, the molecular weight obtained from intrinsic viscosity measurement was greater than the expected molecular weight. This may be attributed to the branching and/or crosslinking reaction through Claisen-type condensation reactions. © 1995 John Wiley & Sons, Inc.
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  • 16
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 799-805 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: UV-curable polyurethane (PU) acrylates have been synthesized from polypropylene glycol (PPG), isophoron diisocyanate (IPDI), and three types of reactive diluents, i.e., 2-hydroxyethylacrylate (HEA), tripropyleneglycol diacrylate (TPGDA), and trimethylolpropane triacrylate (TMPTA). The effects of soft segment length, type, and concentration of reactive diluent on the mechanical and dynamic mechanical properties have been determined. When the soft segment length was short (750) tensile strength (σb) decreased, and elongation at break (εb) generally increased with increasing HEA concentration, due respectively to the inferior strength of HEA homopolymer, and increased molecular weight between crosslinks (Mc). Initial modulus (E) and σb increase and elongation at break (εb) decreased with the increase of TPGDA concentration, and the effect was more pronounced as the soft segment length decreased. The hardness and σb increase with diluent concentration in PPG 2000-based materials was more pronounced with higher functionality diluent, due to the increased crosslinking density. The lower temperature glass transition peak of PU was not influenced by the TPGDA incorporation, whereas the higher temperature one moved toward still higher temperature. This was interpreted in terms of possible compatibility of hard segments and acrylates due to their similar polarity and hydrogen bonding. © 1996 John Wiley & Sons, Inc.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 1773-1778 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In this article, a novel electrolyte system composed of both porous polysulfone film and a propylene carbonate/LiCIO4 liquid solution occupying the pore is suggested. Porous poly-sulfone acts as a support which imparts a good mechanical property and accommodation of a liquid electrolyte. Using this approach, we could enhance the conductivity and me-chanical property of the polymer electrolyte simultaneously. The maximum conductivity of this system was 3.93 × 10-3 S/cm at room temperature. The conductivity seems to be significantly affected by the amount of the uptake of the liquid electrolyte and also by the surface characteristics of the porous polysulfone. The path for ionic conduction is effectively formed with the increase in the uptake of the liquid electrolyte. Low-surface porosity and high-surface roughness is believed to reduce the ionic conduction. However, the denser surface layer of the support showed retarded evaporation of propylene carbonate under reduced pressure, indicating superior long-term stability. © 1996 John Wiley & Sons, Inc.
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  • 18
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 29 (1995), S. 403-409 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Potent and novel fibrinolytic enzymes (lumbrokinase [LK]) were extracted from the earthworm, Lumbricus rubellus. These enzymes were very stable and showed greater antithrombotic activity than other currently used fibrinolytic proteins. An LK fraction showing the most potent fibrinolytic activity was immobilized onto a polyurethane (PU) surface to investigate its enzymatic activity and antithrombotic activity. A methanol-extracted PU surface was coated with 3% (wt/vol) maleic anhydride methylvinyl ether copolymer (MAMEC)/tetrahydrofuran (THF) solution, and the surface was incubated in an LK solution/phosphate-buffered saline (PBS, pH 7.4). The surface properties were characterized by attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR), electron spectroscopy for chemical analysis (ESCA), and dynamic contact angle. The stability of immobilized LK was determined by caseinolytic activity assay and the specificity of immobilized LK on fibrinogen/fibrin was observed by sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE). The antithrombotic activity of immobilized LK was evaluated using an ex vivo rabbit A-A shunt experiment. LK immobilization was confirmed by ATR-FTIR and ESCA. Immobilized LK demonstrated stable proteolytic activity during various incubation periods. Immobilized LK proteolyzed fibrinogen and fibrin almost specifically, while it hardly hydrolyzed other plasma proteins including plasminogen and albumin. In the ex vivo A-A shunt experiment, the LK-immobilized surface significantly prolonged occlusion time over control surfaces. This is primarily due to the high thrombolytic activity of immobilized LK. In this work, a highly efficient surface modification method on the PU surface was developed, and this LK immobilization technique will be very useful in improving the blood compatibility of blood-contacting devices. © 1995 John Wiley & Sons, Inc.
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  • 19
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 36 (1997), S. 200-208 
    ISSN: 0021-9304
    Keywords: vascular graft ; polyester ; porosity ; alginate impregnation ; blood-leak prevention ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Alginate gels are known to be biocompatible, degradable, and nontoxic. In this study, sodium alginate was impregnated into a porous, knitted polyester graft (Microvel® double velour graft) 6 mm in diameter. The alginate-impregnated graft was investigated in vitro and in vivo to evaluate its potential for use as a new vascular graft impervious to blood, while retaining high porosity for tissue ingrowth and biological healing. For in vitro investigation, the coating weight, water permeability, morphology, and mechanical properties of the alginate-impregnated grafts were compared to those of control or commercially available collagen-impregnated (Hemashield®) grafts. The water permeability of the controls (1846 mL/min cm2 at 120 mm Hg) was reduced 〉99% by the alginate impregnation, rendering the graft impervious to blood. The coating weight of the alginate was 45 mg/g of graft, producing a much lower value than that of the collagen-impregnated model (310 mg/g). For in vivo investigation, the alginate-impregnated grafts were implanted in the aorta of mongrel dogs without preclotting for scheduled periods ranging from 4 h to 6 months. The control grafts after preclotting and the collagen-impregnated grafts without preclotting were also implanted for 3 and 6 months for comparison. Gross observation of the explanted grafts and histologic examination of the representative sections were conducted for three types of grafts using a light microscope after hematoxylin-eosin staining. No significant differences were observed between the histologic appearance of the alginate-impregnated grafts and that of the preclotted and collagen-impregnated grafts in terms of the degree of inflammation, foreign-body giant cell reaction, and intimal fibrosis. Endothelial-like cells were present on the midsections of all the grafts after 3 months of implantation. The resorption rate of alginate impregnated into the graft was also examined after staining the sections with periodic acid-Schiff reagent, Toluidine blue, and Alcian blue, which are specific for alginates. The staining alginate was partially visible between the graft fabrics up to 1 month after implantation, but was completely resorbed after 3 months. This preliminary study demonstrated that the use of an alginate as a biological sealant instead of proteins such as collagen, gelatin, and albumin may be a feasible approach to developing imprevious textile arterial prostheses, since the proteins have been reported to be generally unstable, hard to obtain in pure forms, not easy to crosslink and control resorption rate, and difficult to render compatible with standard storage and sterilization procedures. © 1997 John Wiley & Sons, Inc. J Biomed Mater Res, 36, 200-208, 1997.
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  • 20
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 30 (1996), S. 23-30 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Adsorption of proteins (fibrinogen, albumin, and gamma globulin) from plasma onto surface-modified PUs (PU-PEO, PU-SO3, and PU-PEO-SO3) was evaluated. Adsorbed fibrinogen at steady state decreased in the order PU-SO3 〉 PU 〉 PU-PEO-SO3 〉 PU-PEO, suggesting that sulfonate groups have specific high affinity to fibrinogen. The intermediate fibrinogen adsorption on PU-PEO-SO3 can be explained by the compensatory effect between the low protein binding affinity of the PEO chain and the high fibrinogen binding affinity of the sulfonate group. In addition, PU-PEO-SO3 showed a very fast fibrinogen adsorption due to the high accessibility of the sulfonate group to fibrinogen by the poly(ethylene oxide) (PEO) spacer. The kinetic profiles of their surfaces showed that as the adsorption time increases, fibrinogen initially adsorbed was decreased and a plateau reached, demonstrating that all the surfaces exhibited the Vroman effect (the fibrinogen displacement phenomenon). PU-PEO showed the least fibrinogen and albumin adsorption among PUs, confirming the known nonadhesive property of PEO chains. It is very interesting that PU-PEO-SO3 exhibited the highest adsorption of albumin and the lowest adsorption of IgG. Therefore, it may be concluded that such adsorption behaviors of proteins to PU-PEO-SO3 contribute to improved blood compatibility. © 1996 John Wiley & Sons, Inc.
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