1999
DOI: 10.1016/s0141-3910(98)00078-0
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Chemical reactions during the processing of stabilized PE: 1. Discolouration and stabilizer consumption

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Cited by 25 publications
(21 citation statements)
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“…(2), that is, c 0 exp(ϪkЈ 1 n), and the measured OIT values. 1 It was shown 1 that OIT 0 ϭ 0, showing that the neat polymer has a much lower stability than the stabilized samples.…”
Section: Stabilitymentioning
confidence: 99%
See 1 more Smart Citation
“…(2), that is, c 0 exp(ϪkЈ 1 n), and the measured OIT values. 1 It was shown 1 that OIT 0 ϭ 0, showing that the neat polymer has a much lower stability than the stabilized samples.…”
Section: Stabilitymentioning
confidence: 99%
“…1,2 An analysis of the data and additional experiments indicated that all chemical reactions are related to each other. The reactions of the stabilizer lead to color development, [12][13][14][15][16][17] and that of the polymer leads to changes in its molecular structure, which, on the other hand, determine the rheological properties of the granulates 11,18,19 and the mechanical characteristics of the films blown from them.…”
Section: Introductionmentioning
confidence: 99%
“…A number of such transformation products, notably conjugated and nonconjugated quinoidal compounds, have been evaluated for their absorption characteristics in the visible spectrum [1][2][3][4][5][6]. Quinone methides (QM), are the final and oxidation-stable transformation products of mono-and polycyclic phenolic antioxidants that are substituted in positions 2 or 4 to a hydroxyl group with methyl, methylene or methine groups.…”
Section: Introductionmentioning
confidence: 99%
“…These alkyl radicals react with molecular oxygen forming oxidation products, and new alkyl radicals, which restart the oxidation cycle (Figure 1). In this way, during this cycle, the progressive polymer and polymer weight modifications by chain scission or crosslinking result finally in complete mechanical performance loss 9–13. It should be noted that the failure of the mechanical properties of polyethylene in the course of heat aging is also associated with crack formation on the surface and subsequent crack propagation under mechanical stress 13…”
Section: Introductionmentioning
confidence: 99%
“…In the presence of small amounts of oxygen these radicals cannot recombine, but form peroxy radicals (ROO • ) and hydroperoxides (ROOH). Depending on the polymer these chemical reactions result in molecular weight degradation or increase (branching, cross‐linking), and the plastic becomes unsuitable for its original use 9–12…”
Section: Introductionmentioning
confidence: 99%