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Interaction of long‐lived reactive species from cold atmospheric pressure plasma with polymers: Role of macromolecular structure and deep modification of aromatic polymers
Author(s) -
Luan Pingshan,
Oehrlein Gottlieb S.
Publication year - 2019
Publication title -
plasma processes and polymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.644
H-Index - 74
eISSN - 1612-8869
pISSN - 1612-8850
DOI - 10.1002/ppap.201900053
Subject(s) - polystyrene , polymer , styrene , macromolecule , materials science , polymer chemistry , surface modification , attenuated total reflection , x ray photoelectron spectroscopy , fourier transform infrared spectroscopy , chemical engineering , photochemistry , chemistry , organic chemistry , infrared spectroscopy , copolymer , biochemistry , engineering
We report (a) the deep modification of polymers by long‐lived reactive species generated in atmospheric pressure plasma and (b) the dependence of plasma–polymer interaction on the macromolecular structure. Styrene‐based polymers show significant thickness expansion whereas polymers with methyl, alcohol, and ether side groups show low‐rate etching. The characterization of polystyrene (PS) by X‐ray photoelectron spectroscopy and attenuated total reflectance–Fourier transform infrared shows that plasma treatment destroys aromatic rings and produces ether, ester, and surface organic nitrate groups. These modifications can happen at tens of nanometers below the surface, which we attribute to the reaction–diffusion of plasma species. Comparing three styrene‐based polymers namely PS, poly(4‐methyl styrene), and poly(α‐methyl styrene), we find that long‐lived species primarily attack the C–H bond on the carbon site where the aromatic ring connects.