TY - JOUR
T1 - Influence of the bulk and surface morphology on adhesion of polystyrene‐inter‐poly‐cross‐2‐ethylhexyl‐methacrylate films and particles
AU - de Graaf, Leontine A.
AU - Albers, Pieter-Jan W.
AU - Möller, Martin
PY - 1995
Y1 - 1995
N2 - The adhesion behavior of semi-interpenetrating polymer networks (semi-IPNs) of linear polystyrene (PS) in crosslinked poly-2-ethylhexylmethacrylate (EHMA) was studied by variation of the bulk and surface morphology, i.e., domain size, continuity, and concentration in the domains. Semi-IPNs were prepared by liquid-liquid demixing upon cooling of a homogeneous solution of PS in methacrylate monomer, followed by gelation of the PS-rich phase and UV polymerization of the methacrylate resin. Welding of films allowed the preparation of larger objects provided that (1) the samples were phase separated to a high degree and contained domains with a high PS concentration (>90%) and (2) polystyrene was present at the interface. For semi-IPN films, a linear dependence of the adhesion strength on the (crack healing time)1/4 was obtained. Based on these considerations, a process was developed to obtain melt-processable semi-IPN particles, by quenching droplets of the polymer solution into a cold liquid. These particles obtained a PS-rich skin layer and showed good adhesion after blending with a thermoplast.
AB - The adhesion behavior of semi-interpenetrating polymer networks (semi-IPNs) of linear polystyrene (PS) in crosslinked poly-2-ethylhexylmethacrylate (EHMA) was studied by variation of the bulk and surface morphology, i.e., domain size, continuity, and concentration in the domains. Semi-IPNs were prepared by liquid-liquid demixing upon cooling of a homogeneous solution of PS in methacrylate monomer, followed by gelation of the PS-rich phase and UV polymerization of the methacrylate resin. Welding of films allowed the preparation of larger objects provided that (1) the samples were phase separated to a high degree and contained domains with a high PS concentration (>90%) and (2) polystyrene was present at the interface. For semi-IPN films, a linear dependence of the adhesion strength on the (crack healing time)1/4 was obtained. Based on these considerations, a process was developed to obtain melt-processable semi-IPN particles, by quenching droplets of the polymer solution into a cold liquid. These particles obtained a PS-rich skin layer and showed good adhesion after blending with a thermoplast.
KW - Interpenetrating polymer networks (semi-)
KW - Polystyrene
KW - Polymethacrylate
KW - Adhesion
U2 - 10.1002/(SICI)1099-0488(199608)34:11<1839::AID-POLB1>3.0.CO;2-N
DO - 10.1002/(SICI)1099-0488(199608)34:11<1839::AID-POLB1>3.0.CO;2-N
M3 - Article
SN - 0098-1273
VL - 34
SP - 1839
EP - 1852
JO - Journal of polymer science. Polymer physics edition
JF - Journal of polymer science. Polymer physics edition
IS - 11
ER -