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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 2854-2861 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 31 (1993), S. 715-721 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract This paper describes a new method for rubber toughening brittle powder coatings. The design involves the use of toughening agents with specific physical and chemical properties. The modifiers are low-to-medium molecular weight polymers with polymerizable end groups (macromonomers). To achieve the physical properties required for fabrication into fine powders for subsequent deposition using conventional powder coating equipment, semi-crystalline polymers with Tg's well below room temperature and melting points above ≈70°C were required. Upon copolymerization with a thermosetting resin, crystallization of the modifier was precluded provided that low ethylene oxide compositions were employed. This scheme, in principle, yields an amorphous low Tg modifier chemically bound to the cured network. Poly(ethylene oxide), PEO, was found to be an excellent candidate, since it has a Tg of -68°C and a Tm of 70°C, sufficient crystallinity for friability and functional end groups for copolymerization. Free radical polymerization of 2,2-bis[4-vinylbenzoyloxyphenyl] hexafluoropropane and step-growth polymerization of 4,4′-(hexafluoroisopropylidene)diphenyl cyanate were utilized to demonstrate the feasibility of this approach. An electrostatic powder coater was used to co-deposit the PEO macromonomers with either of the thermosetting precursor monomers, followed by thermal curing to produce the modified networks. The resulting networks showed multiphase morphologies with improved toughness.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract. The fracture toughness has been investigated with single edge notched bending specimens in solvent-modified epoxies, which were prepared via the Chemically Induced Phase Separation technique. The generation of a controlled morphology with liquid droplets in the micrometer range leads to a substantial increase in the fracture energy of nearly 400% compared to the non-modified epoxy network. The critical stress intensity factor of these highly crosslinked thermosets does not vary significantly. These results demonstrate the general potential of the Chemically Induced Phase Separation technique to prepare porous thermosets, thus combining increased toughness with lowered density.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 276 (1998), S. 853-859 
    ISSN: 1435-1536
    Keywords: Key words Gold clusters ; graft copolymer ; nanocomposites ; optical properties ; TEM
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  An amphiphilic poly(acrylic acid)/polystyrene graft copolymer (PAA-g-PS) has been used to form “nanoreactors” for the synthesis of gold clusters. Such copolymers tend to form stable micelles in non-polar organic solvents where the poly(acrylic acid) chains constitute the core, and the polystyrene chains, the shell. In the present study, the micellar structure of PAA-g-PS in toluene has been demonstrated by dynamic light scattering and transmission electron microscopy (TEM). The subsequent preparation of gold-graft copolymer composites involved the introduction of gold chloride (AuCl3), either in powder form or previously dissolved in ether, into the micellar cores of the PAA-g-PS in toluene. The gold salt was then reduced by ultraviolet (UV) irradiation of the emulsion, or of dried cast films. TEM and ultraviolet-visible (UV/Vis) spectroscopy were used to characterize the resulting composites. Gold particles of less than 5 nm in diameter were observed in all cases, but the size distribution and the spatial arrangement of the clusters in the cast films were modified when diethyl ether was used to introduce AuCl3 into the PAA-g-PS micellar cores. This was thought to be due to enhanced nucleation of the gold particles and partial disruption of the micellar cores in the presence of diethyl ether.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 2879-2888 
    ISSN: 0887-624X
    Keywords: thermosetting cyanate networks ; foams ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A general means of generating nanofoams from thermosetting materials was investigated. Foams were prepared from a thermosetting monomer copolymerized with a thermally labile material, such that the thermally labile coblock is the dispersed phase. Upon thermal treatment, the thermally unstable block undergoes thermolysis, leaving pores where the size and shape are dictated by the initial morphology. For this investigation the thermosetting resin was prepared from a cyanate monomer (4,4′-(hexafluoroisopropylidene) diphenyl-cyanate), with either poly(propylene oxide) or a propylene oxide-urethane copolymer as the thermally labile block. The propylene oxide-based oligomers were molecularly miscible with the cyanate resin over the entire range of compositions, and molecular weights investigated, but developed a two-phase structure upon reaction to form the polycyanurate thermoset. The molecular weight and composition of propylene oxide chemically incorporated into the polycyanurate was varied along with the curing condition, solvents, and catalyst. Dynamic mechanical and small-angle x-ray scattering measurements demonstrated a two-phase morphology in the cured networks wherein the propylene oxide domains are dispersed in the polycyanurate matrix. Upon decomposition of the propylene oxide component, however, the foam was found to collapse. Samples with the larger void size retained, to a large extent, their void composition upon the thermolysis of the propylene oxide component. © 1996 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 2177-2192 
    ISSN: 0887-6266
    Keywords: blend ; triblock copolymer ; crazing ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: We have prepared triblock copolymers of poly(phenylene oxide) (PPO) and polysulphone (PSF) of the form PPO-PSF-PPO in order to assess their intrinsic mechanical properties and their potential as interfacial compatibilizers in polystyrene/PSF blends. For sufficiently long polysulphone block lengths, we observed microphase separation both in the triblock copolymers and in their blends with polystyrene. The triblock polymers, nevertheless, showed very similar microdeformation behavior to the PPO homopolymer, suggesting the phase separation to play a minor role. On the other hand, the compatibility of the poly(phenylene oxide) blocks and polystyrene ensured a high degree of interphase adhesion in blends containing both polystyrene and free PSF, even for relatively high homopolymer molecular weights. © 1996 John Wiley & Sons, Inc.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1813-1820 
    ISSN: 0887-6266
    Keywords: nanofoams ; polyimides ; crazing ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Transmission electron microscopy has been used to investigate the microdeformation behavior of thermally imidized thermoplastic pyromellitic dianhydride/1,1-bis(4-amino-phenyl)-1-phenyl-2,2,2 trifluoroethylene (3FDA/PMDA) polyimide films with a Tg of ∼ 440°C, prepared by solution casting of a polyamic ester precursor. Failure of the films at room temperature was by unstable cracking at about 5% strain, accompanied by homogeneous shear deformation at the crack tips. As the temperature was raised to above 100°C, zones of mixed shear and crazing were observed, and a stick-slip mode of cracking. Above about 300°C shear was once again the dominant deformation mechanism and the films became fully ductile. In films containing porosity on a scale of a few nanometers, prepared by thermal degradation/imidization of a 3FDA/PMDA/poly α-methyl styrene graft copolymer, film failure at room temperature was also by unstable cracking, but a zone of multiple craze-like features was observed at crack tips, rather than a single shear deformation zone. The increase in extent of this zone of craze-like features as the temperature was raised was again associated with an increase in crack stability. ©1995 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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