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  • 1
    Electronic Resource
    Electronic Resource
    Surface modification and adhesion characteristics of polycarbonate films after graft copolymerization (1998)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 357-366 
    Details
    ISSN: 0887-624X
    Keywords: surface graft copolymerization ; adhesive-free adhesion ; polycarbonate ; XPS ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The surfaces of ozone-pretreated polycarbonate films were subjected to further modification by thermally induced graft copolymerization with acrylic acid (AAc), sodium salt of styrene sulfonic acid (NaSS), N,N-dimethylacrylamide (DMAA), N,N-(dimethylamino)ethyl methacrylate (DMAEMA) and 3-dimethyl(methacryloyl ethyl)-ammonium propanesulfonate (DMAPS) monomers. The structure and composition at the copolymer interface were studied by angle-resolved X-ray photoelectron spectroscopy (XPS). For polycarbonate films with a substantial amount of grafted polymer, the hydrophilic graft penetrates or becomes partially submerged beneath a thin surface layer of dense substrate chains. This microstructure was further supported by the water contact angle measurements. Adhesive-free adhesion studies revealed that the AAc, DMAA or DMAPS graft copolymerized polycarbonate film surface adhered strongly to another similarly modified surface (homo-interface) when brought into direct contact in the presence of water and subsequently dried. The development of the lap shear strength is dependent on the concentration of the surface graft, the microstructure of the grafted surface, the adhesion (drying) time, and the nature of the interfacial interaction. The simultaneous presence of chain entanglement and electrostatic interaction readily results in substantially enhanced adhesion strengths between two DMAPS graft copolymerized surfaces or between an AAc and a DMAA graft copolymerized surface (hetero-interface). XPS analyses of the delaminated surfaces suggest that failure occurred cohesively below the graft-substrate interface. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 357-366, 1998
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Surface modification of polytetrafluoroethylene films via graft copolymerization for auto-adhesion (1998)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 3107-3114 
    Details
    ISSN: 0887-624X
    Keywords: PTFE ; auto-adhesion ; surface grafting ; amphoteric monomer ; Ar plasma ; XPS ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The surfaces of Ar plasma-pretreated polytetrafluoroethylene (PTFE) films are further functionalized via UV-induced graft copolymerization with amphoteric N,N′-dimethyl(methacryloylethyl)ammonium propansulfonate (DMAPS) either in Ar atmosphere, or under atmospheric conditions and in the absence of a polymerization initiator. The so-modified PTFE films from either process are capable of exhibiting adhesive-free adhesion or auto-adhesion with one another when brought into intimate contact in the presence of a small quantity of water. The lap shear adhesion strength increases with increasing graft concentration and can readily exceed the yield strength of the PTFE substrate. Two plasma-pretreated PTFE films also readily undergo thermal graft copolymerization with concurrent lamination when lapped together in the presence of a small quantity of the DMAPS monomer solution at elevated temperature in the atmosphere. The surface compositions of the graft-copolymerized PTFE films and the delaminated surfaces were characterized by X-ray photoelectron spectroscopy (XPS). In most cases, adhesional failure occurred near the graft-substrate interphase. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 3107-3114, 1998
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Surface structures of fluoropolymer, polyolefin and polyester films after modification by graft polymerization (1994)
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 5 (1994), S. 837-842 
    Details
    ISSN: 1042-7147
    Keywords: Polyolefin ; Fluoropolymer ; Polyester ; Graft Polymerization ; Surface structure ; XPS ; SIMS ; 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: Pristine and argon plasma pretreated polytetrafluoroethylene (PTFE), polystyrene (PS), high-density polyethylene (HDPE) and poly(ethylene terrephthalate) (PET) films have been subjected to near-UV light-induced graft polymerization with water-soluble acrylamide (AAm), the sodium salt of styrene sulfonic acid (NaSS), acrylic acid (AAc) and N,N-dimethylaminoethylmethylacrylate (DMAEMA) monomers. The structure and composition at the substrate surface with grafted polymer were studied by angle-resolved X-ray photoelectron spectroscopy (XPS). In most cases, the density of surface grafting is enhanced by plasma pretreatment. For each polymer substrate with a substantial amount of grafting, the hydrophilic graft penetrates or becomes partially submerged beneath a thin surface layer of dense substrate chains. This stratified microstructure is consistent with the static secondary ion mass spectroscopy (SIMS) and Ar+ beam depth profiling results. The two latter techniques also suggest that when the grafted polymer has a bulky substituent, there is less efficient penetration of the grafted polymer below the surface.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pat.1994.220051211
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