2003
DOI: 10.5271/sjweh.717
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Effects of thermal degradation products from polyurethane foams based on toluene diisocyanate and diphenylmethane diisocyanate on isolated, perfused lung of guinea pig

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Cited by 9 publications
(10 citation statements)
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“…39 -41 Similar observations have been made for polyether-urethane 42,43 ; however, the same scientist has found a contradicting evidence. 44 The monomers could have been cracked free from the polyether-urethane structure during processing, [45][46][47] since the molecular weight was changed during production of the polymer sample. Processing degradative behavior is further discussed in the next section.…”
Section: Discussionmentioning
confidence: 99%
“…39 -41 Similar observations have been made for polyether-urethane 42,43 ; however, the same scientist has found a contradicting evidence. 44 The monomers could have been cracked free from the polyether-urethane structure during processing, [45][46][47] since the molecular weight was changed during production of the polymer sample. Processing degradative behavior is further discussed in the next section.…”
Section: Discussionmentioning
confidence: 99%
“…This leads to release of MDA. Other degradation products may also be produced 28. However, this study has focused on the detection of MDA, as it might be the most toxic of the degradation products from polyether–urethane 18.…”
Section: Methodsmentioning
confidence: 99%
“…Other degradation products may also be produced. 28 However, this study has focused on the detection of MDA, as it might be the most toxic of the degradation products from polyether-urethane. 18 The release of the toxic breakdown product methylene dianiline (MDA) from the material was considered to be possible.…”
Section: Degradation Productmentioning
confidence: 99%
“…Given their importance, it is no surprise that there is a considerable literature on the thermal degradation chemistry of polyurethanes [see for example [1][2][3][4][5][6][7][8][9][10][11][12][13], although studies on foam materials are more limited in number, with many studies focussing on elastomers or model compounds.…”
Section: Introductionmentioning
confidence: 99%
“…It is generally accepted that the purely thermal degradation of the urethane linkages within polyurethane (the primary degradation step) occurs between 200°C and 250°C by one or more of three mechanisms: (i) a simple depolymerisation to regenerate isocyanate and hydroxyl groups, (ii) a six-membered cyclic transition state producing amine and alkene chain ends and CO 2 , (iii) a four-membered transition state liberating CO 2 without chain scission. It has been reported by many authors that the depolymerisation reaction (i) is the predominant degradation reaction for the urethane linkage [2,3,[5][6][7].…”
Section: Introductionmentioning
confidence: 99%