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  • 1
    Electronic Resource
    Electronic Resource
    Postirradiation polymerization of vinyl monomers on poly(ethylene terephthalate) (1986)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 31 (1986), S. 509-519 
    Details
    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 postirradiation process was evaluated in polymerizing vinyl monomers on poly(ethylene terephthalate) (PET) film, fiber, and fabric. The use of DMF, pyridine, and DMSO as swelling agents to facilitate monomer incorporation and effective polymerization were also investigated. The solvents were effective in promoting the incorporation of acrylic acid (AA) in PET film and that of n-vinyl-2-pyrrolidinone (VP) in Dacron 54. AA, a good swelling agent for PET, produced equivalent polymerization yield and moisture regain results with or without any solvent on Dacron 54 and 64. Polymerization yields on films increased with increasing total doses, but those on yarns and fabrics were independent of total dose. The different results obtained on film versus yarn and fabric from solvent treatment and total dose is thought to be due to the different surface-volume ratio of these substrates. The moisture properties of the substrates were dependent mainly upon the monomer type. Among the monomers studied, VP gave highest moisture regain values, followed by AA. The tensile properties of the modified Dacron 54 were not affected. However the breaking elongation of the modified Dacron 64 was slightly lowered by postirradiation polymerization without solvent treatment and was increased when solvent treatment was included.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1986.070310218
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  • 2
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    Accretion rates in coastal wetlands of the southeastern Gulf of California and their relationship with sea-level rise (2016)
    Sage
    In: Holocene
    Details
    Publication Date: 2016-06-28
    Description: Sea-level rise (SLR) is one of the most conspicuous examples of the environmental impact of recent climate change. Since SLR rates are not uniform around the planet, local and regional data are needed for proper adaptation plans. 210 Pb-dated sediment cores were analyzed to determine the trends of sediment accretion rates (SARs) at three tropical saltmarshes in the Estero de Urias lagoon (Gulf of California, Mexico), in order to estimate the SLR trends during the past ~100 years, under the assumption that these ecosystems accrete at a similar rate to SLR. A chemometric approach, including multivariate statistical analysis (factor analysis) of geochemical data (including 13 C; 15 N; C/N ratios; and Br, Na, and Cl as proxies for marine transgression) was used to identify the marine transgression in the sediment records. Based on core geochemistry, only one of the three cores provided a long-term record attributable to marine transgression. SLR trends, estimated from SARs, showed increasing values, from a minimum of 0.73 ± 0.03 mm yr –1 at the beginning of the 20th century and up to 3.87 ± 0.12 mm yr –1 during the period 1990–2012. The estimated SLR trend between 1950 and 1970 was comparable to the tide gauge records in Mazatlan City for the same period. Results showed the caveats and strengths of this methodology to reconstruct decadal SLR trends from the sedimentary record, which can be used to estimate long-term SLR trends worldwide in regions where monitoring data are scarce or absent.
    Print ISSN: 0959-6836
    Electronic ISSN: 1477-0911
    Topics: Geography , Geosciences
    Published by Sage
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  • 3
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    Surface states characterization in the strongly interacting graphene/Ni(111) system (2018)
    Institute of Physics (IOP)
    Details
    Publication Date: 2018-10-30
    Description: By combining nonlinear photoemission experiments and density functional theory calculations, we study the modification of Ni(111) surface states induced by the presence of graphene. The main result is that graphene is able to displace the Ni(111) surface states from the valence band close to the Fermi level uncovering the d -band of Ni. The shift of the surface states away from the Fermi level modifies their k -dispersion and the effective mass. The unoccupied image state of graphene/Ni(111) has been also characterized. The ab initio calculations give a theoretical insight into the electronic properties of graphene/Ni(111) in the two stable top-fcc and top-bridge phases showing that the interface properties are poorly dependent on the stacking. The screening properties to an externally applied electric field are also discussed.
    Electronic ISSN: 1367-2630
    Topics: Physics
    Published by Institute of Physics (IOP)
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