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. 2013 Jun 26;46(13):5117–5132. doi: 10.1021/ma401014h

Table 1. Thermal Events for Bis-Benzoxazine Monomers As Determined by DSCa.

              ΔHp
 
monomer additive [additive] (mol %) Tg1 (°C) Top (°C) Tmax (°C) Tep (°C) (J g–1) (kJ mol–1/Bz) Tg2 (°C)
BA-a     39 203 240 283 299 69.2 157
BA-ab     106 218 257 292 304 70.3 162
BA-a TDP 1 37 196 243 293 311 71.9 154
BA-a TDP 2.5 38 186 233 295 318 73.6 160
BA-a TDP 5 37 187 235 295 318 73.6 153
BA-a TDP 10 36 178 226 295 324 74.9 153
BA-a TDP 12 37 172 222 298 331 76.6 154
BA-a TDP 25 38 154 214 294 322 74.5 155
BA-a TDA 1 37 186 234 296 241 55.7 164
BA-a TDA 3.1 37 172 225 298 358 82.8 164
BA-a TDA 5 37 157 216 295 324 74.9 168
BA-a TDA 10 38 111 196 274 365 84.4 174
BA-a TDA 15 38 145 198 293 388 89.7 184
BA-a TDA 31 39 133 188 268 292 67.5 187
BF-a     36.2 170 232 292 311 67.4 174
BF-a TDP 12 34.6 132 218 295 300 65.2 164
BF-a TDA 15 35.0 130 196 287 294 63.9 199
BT-a       173 221 278 350 79.2 173
BT-a TDP 12   144 209 278 316 71.5 196
BT-a TDA 15   146 191 269 315 71.3 180
a

Tg1 = possible glass transition or melting transition of monomer determined using a heating rate of 10 K min–1; Top = observed onset of polymerization; Tmax = temperature of exothermic peak maximum; Tep = observed end of polymerization; ΔHp = enthalpy of exothermic peak (both as J/g of monomer and kJ/mol–1 of benzoxazine ring); Tg2 = glass transition temperature of polymer determined using a heating rate of 10 K min–1; TDP = 3,3′-thiodiphenol; TDA = 3,3′-thiodipropionic acid.

b

Recrystallized.