REACTIVE PROCESSING OF POLYETHYLENE - EFFECT OF PEROXIDE-INDUCED GRAFT-COPOLYMERIZATION OF SOME ACRYLIC-MONOMERS ON POLYMER STRUCTURE MELT RHEOLOGY AND RELAXATION BEHAVIOR
P. Ghosh et D. Dev, REACTIVE PROCESSING OF POLYETHYLENE - EFFECT OF PEROXIDE-INDUCED GRAFT-COPOLYMERIZATION OF SOME ACRYLIC-MONOMERS ON POLYMER STRUCTURE MELT RHEOLOGY AND RELAXATION BEHAVIOR, European Polymer Journal, 34(10), 1998, pp. 1539-1547
Melt processing of polyethylene (PE) at 170 degrees C in a shear mixer
in the presence of selected doses of dicumyl peroxide (DCP) and an ac
rylic monomer (acrylic acid (AA), ethyl acrylate (EA) and butyl acryla
te (BA)) resorted in synthesis of acrylic grafted PE via radical graft
copolymerization. The graft copolymers of PE, made free from the resp
ective acrylic homopolymers by appropriate solvent extraction, showed
development of higher shear stress (tau) compared to the control (ungr
afted) PE and simply DCP-treated PE when sheared at different rates (D
) at different temperatures (160-190 degrees C). Melts of the graft co
polymers of PE and DCP-treated PE, much like the melt of the control P
E showed pseudoplastic flow behavior and all of them assumed a more pr
onounced pseudoplastic character over a range of relatively high rates
of shear and at a relatively low melt temperature. The rupture shear
parameters, measure of thixotropic hysteresis and relaxation behaviors
of the differently modified PE and the control PE have been evaluated
and compared. Observed effects and odd trends have been understood an
d interpreted considering (a) establishment of crosslinkages in the PE
chains due to peroxide action that become much restricted in the pres
ence of an acrylic monomer used for graft copolymerization, (b) uncert
ain and uncontrolled degree of chain entanglements resulting from poss
ible uneven distributions of the peroxide and monomer in the PE melt d
uring the reactive processing, (c) enhancement in molecular weight on
grafting and (d) disappearance of residual crystalline orientations in
the PE melt above 170 degrees C. (C) 1998 Elsevier Science Ltd. All r
ights reserved.