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https://doi.org/10.1002/pat.1994.220051211
Title: | Surface structures of fluoropolymer, polyolefin and polyester films after modification by graft polymerization | Authors: | Kang, E.T. Neoh, K.G. Tan, K.L. Loh, F.C. Liaw, D.J. |
Keywords: | Fluoropolymer Graft polymerization Polyester Polyolefin SIMS Surface structure XPS |
Issue Date: | Dec-1994 | Citation: | Kang, E.T.,Neoh, K.G.,Tan, K.L.,Loh, F.C.,Liaw, D.J. (1994-12). Surface structures of fluoropolymer, polyolefin and polyester films after modification by graft polymerization. Polymers for Advanced Technologies 5 (12) : 837-842. ScholarBank@NUS Repository. https://doi.org/10.1002/pat.1994.220051211 | Abstract: | Pristine and argon plasma pretreated polytetrafluoroethylene (PTFE), polystyrene (PS), high-density polyethylene (HDPE) and poly(ethy1ene terephthalate) (PET) films have been subjected to near-UV light-induced graft polymerization with water-soluble acylamide (AAm), the sodium salt of styrene sulfonic acid (NaSS), ac y l i c 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. © 1994 by John Wiley & Sons, Ltd. | Source Title: | Polymers for Advanced Technologies | URI: | http://scholarbank.nus.edu.sg/handle/10635/91737 | ISSN: | 10427147 | DOI: | 10.1002/pat.1994.220051211 |
Appears in Collections: | Staff Publications |
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