1985
DOI: 10.1002/adv.1985.060050203
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Modification of molecular weight and flow properties of thermoplastics

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Cited by 50 publications
(28 citation statements)
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“…PA12 has excellent solvent and oil resistance, in particular acid and alkali resistance and excellent environmental stress cracking resistance at elevated temperature [29]. Cross-linking of the PDMS rubber phase by organic peroxides suffers from scorching problems at high mixing temperature due to the faster decomposition of the peroxides (normally used for curing) [30,31]. To overcome this difficulty three structurally different peroxides, namely dicumyl peroxide (DCP), 3,3,5,7,7-pentamethyl 1,2,4-trioxepane (PMTO) and cumyl hydroperoxide (CHP) were chosen for investigation.…”
Section: G Heinrichmentioning
confidence: 99%
“…PA12 has excellent solvent and oil resistance, in particular acid and alkali resistance and excellent environmental stress cracking resistance at elevated temperature [29]. Cross-linking of the PDMS rubber phase by organic peroxides suffers from scorching problems at high mixing temperature due to the faster decomposition of the peroxides (normally used for curing) [30,31]. To overcome this difficulty three structurally different peroxides, namely dicumyl peroxide (DCP), 3,3,5,7,7-pentamethyl 1,2,4-trioxepane (PMTO) and cumyl hydroperoxide (CHP) were chosen for investigation.…”
Section: G Heinrichmentioning
confidence: 99%
“…Nonetheless, careful control is required at all times, particularly in the case of polypropylene, as chain scission can easily occur, decreasing molecular weight and reducing overall efficiency and hence performance [42,43]. In the case of polypropylene the methylene group stabilises the tertiary carbon free radial thus making it more vulnerable to β chain scission, according the reaction mechanism illustrated in Fig. 14.10.…”
Section: Chemistry and Synthesis Of Adhesivesmentioning
confidence: 99%
“…5 Given the fast rate of alkyl radical trapping by nitroxyls, we can assume that initiator-derived radicals produced in the presence of nitroxyl will be quenched. Under this assumption, t ind marks the time where all nitroxyl functionality is consumed, at which point the DCP conversion will equal the trapping ratio, [nitroxyl]/(2[ROOR] 0 ).…”
Section: ■ Introductionmentioning
confidence: 99%