1988
DOI: 10.1016/0032-3861(88)90096-1
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Flame retardant polyphosphate esters: 1. Condensation polymers of bisphenols with aryl phosphorodichloridates: synthesis, characterization and thermal studies

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Cited by 119 publications
(60 citation statements)
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“…The high T d in the resulting epoxy resins may be attributed to the high aromatic content of the DOPO. It may also be attributed to the cyclic OAPOO chain being more thermally stable than the open OAPOO chain, 6,7,13,14 which means that an introduction of doubly stranded units into the backbone may enhance their thermal stability. 8 -12 Char yields of IIP/DDS series epoxy resins were higher than that of DGEBA/DDS under air.…”
Section: Tga Analysismentioning
confidence: 95%
“…The high T d in the resulting epoxy resins may be attributed to the high aromatic content of the DOPO. It may also be attributed to the cyclic OAPOO chain being more thermally stable than the open OAPOO chain, 6,7,13,14 which means that an introduction of doubly stranded units into the backbone may enhance their thermal stability. 8 -12 Char yields of IIP/DDS series epoxy resins were higher than that of DGEBA/DDS under air.…”
Section: Tga Analysismentioning
confidence: 95%
“…[13][14][15][16][17][18][19][20][21] Flameretardant epoxy resins can be obtained by chemically bonding flame-retardant groups onto epoxy resins, and the permanent attachment of a flame retardant frequently leads to high efficiency in flame retardancy. [17][18][22][23] In this study, a rigid phosphorus-containing reactive 2-(6-oxido-6-H-dibenzo[c,e][1,2] oxaphosphorin-6-yl)-1,4-benzenediol (ODOPB) is converted to a phosphorus-containing epoxy resin, 6-H-dibenz[c,e][1,2] oxaphosphorin-6-[2,5-bis-(oxiranylmethoxy)phenyl]-6-oxide (DOPO epoxy resin), which is expected to exhibit the required flame retardancy, less fumes, and higher thermal stability than the conventional flame-retardant epoxy resin systems containing tetrabromobisphenol A (TBBA).…”
Section: Introductionmentioning
confidence: 99%
“…A secondary phosphorus-rich residue which forms a protective layer on the polymer. [16][17][18][19] Therefore the flammaamine was used at a later stage in the reaction to react with unreacted {P{Cl groups to convert bility is reduced by the formation of a char by the phosphorus-containing materials. 20 The higher them to {P{N linkages.…”
Section: Discussionmentioning
confidence: 99%