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. 2017 Jan 17;22(1):149. doi: 10.3390/molecules22010149

Table 6.

Poly-aromatic epoxy monomers from crude bio-mass and thermal properties of the cured materials.

Epoxy Curing Agent Tg (°C) or Tα (°C) Td,5% (°C) Reference
Materials DGEBA Comparison
Epoxidized depolymerized kraft lignin Diethylenetriamine - - 252 d [186]
4,4-diaminodiphenyl methane - - 290 d
Epoxidized depolymerized organosolv lignin Diethylenetriamine - - 228 d
4,4-diaminodiphenyl methane - - 257 d
graphic file with name molecules-22-00149-i036.jpg Phenol Novolac 94 95 - [189]
graphic file with name molecules-22-00149-i037.jpg 134 -
Epoxidized lignin (Cedar) Phenol Novolac (TD2131) - - 293 [190]
Lignin (Cedar) - - 296
Epoxidized lignin (Eucalyptus) Phenol Novolac (TD2131) - - 275
Lignin (Eucalyptus) - - 274
Epoxidized lignin (Bamboo) Phenol Novolac (TD2131) - - 266
Lignin (Bamboo) - - 259
Epoxidized green tea extract Isophorone Diamine 142 a,b 140 a,b 256/267 c [193]
Epoxidized cardanol (NC514) Isophorone Diamine 50 a,b 155 a,b 350 [205]
Jeffamine T403 23 70 352 e [198]
Isophorone Diamine 41 121 350 e
50/59 b 158/158 b 366 e/363 c,e [196]
Jeffamine D400 15/9 b - 362 e/361 c,e
PE-C9-NH2 13 279 - [141]
PE-C18-NH2 14 284 -
Phenalkamine NX5454 30/38 a,b - 325 f/322 c,f [206]
Cardanol cysteamine 19/21 a,b - 328 f/311 c,f

a Tα measured by DMA at the peak position of loss modulus curve; b Tα measured by DMA at the maximum of tan δ; c Td under air flow; d IDT = initial decomposition temperature; e Td,30%; f Td,10%.