A look inside the extruder: Evolution of chemistry, morphology and rheology along the extruder axis during reactive processing and blending

Citation
M. Van Duin et al., A look inside the extruder: Evolution of chemistry, morphology and rheology along the extruder axis during reactive processing and blending, MACRO SYMP, 170, 2001, pp. 29-39
Citations number
26
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
MACROMOLECULAR SYMPOSIA
ISSN journal
10221360 → ACNP
Volume
170
Year of publication
2001
Pages
29 - 39
Database
ISI
SICI code
1022-1360(200106)170:<29:ALITEE>2.0.ZU;2-D
Abstract
A simple device was recently developed for fast sampling (within a few seco nds) of representative melt samples (about 2 g) on a running extruder. An a rray of such devices has been mounted on a twin-screw extruder. The goal of this study was to de-black-box reactive processing of polymers by studying some typical examples. Processing of polyolefins in the presence of peroxides: when the polymer is molten and the melt temperature is sufficiently high branching/cross-linki ng of PE and degradation of PP occurs; the conversion follows a convex prof ile along the screw axis, which profile is similar to the exponential profi le calculated for peroxide decomposition. Free-radical grafting of maleic anhydride (MA) onto polyolefins: MA graftin g onto PE and PP also follows a convex profile with branching/cross-linking as parallel side reaction for PE and degradation for PP; for PE degradatio n of the formed grafted/cross-linked gel is observed at the end of the extr uder. Reactive blending of PA-6 with EPM-g-MA: within a few seconds the in-situ c ompatibilization reaction, resulting in PA-6/EPM graft copolymers, is compl eted and the degree of rubber dispersion has changed from the mm to the sub -mum range, regardless of the MA content of EPM-g-MA and the EPM-g-MA conte nt of the blend; PA degradation occurs along the whole extruder.