Macromolecular Research, Vol.29, No.7, 462-469, July, 2021
An Acid-/Base-Degradable Epoxy Resin Cured by 1,3,5-Triacroylamino-hexahydro-s-triazine Derivative
E-mail:,
The degradation and recycling of waste epoxy resin products is an urgent environmental problem. To solve this issue, we use acid-/base-degradable 1,1’,1"- (1,3,5-hexahydro-s-triazine-1,3,5-triyl) tris(3-ethylamino-propan-1-one) (TAHT-EA) as curing agent to introduce the hexahydro-s-triazine (HT) ring structure into the cross-linking network to prepare degradable epoxy resin. Specifically, 1,3,5 triacryloylhexahydro-1,3,5-triazine (TAHT) and ethylamine quickly complete the Aza-Michael addition reaction at the interface of chloroform and water droplets under the catalysis of water. The FTIR spectra, NMR spectrum and mass spectrum show that mono- and bis-addition products of ethylamine coexist in the product in which the content of the primary addition product reaches 97%. TAHT-EA can be decomposed by acid and base solutions. Through NMR analysis of the degradation products, it can be explained that the degradation mechanisms are different. The breaking of amide bonds and HT rings in acid solution and the cracking of amide bonds in base solution are speculated to be the main mechanisms under these two different circumstances, respectively. We tested the mechanical, thermal and degradation properties of the epoxy resin cured by TAHT-EA, and compared it with the epoxy resin cured by 4,4'-diaminodiphenylmethane and triethylenetetramine. TAHT-EA-cured epoxy resin shows comparable mechanical properties with Young’s modulus up to 2.05 GPa and tensile strength up to 70.9 MPa. What is more, it degrades completely by 1 M H+/OH- solution at 60℃ within 36 h. Nevertheless, it exhibited a relatively low crosslinked density (633 mol/m3) and low heat resistance (the initial decomposition temperature is lower than 205℃). Overall, TAHT-EA cured epoxy resin has the potential to gradually replace traditional thermosetting resin, thereby solving the environmental problems caused by discarded epoxy resin products.
Keywords:degradable epoxy resin;hexahydro-s-triazine derivative;degradation property;degradation mechanism
- Johnson LM, Ledet E, Huffman ND, Swarner SL, Shepherd SD, Durham PG, Rothrock GD, Polymer, 64, 84 (2015)
- Takahashi A, Ohishi T, Goseki R, Otsuka H, Polymer, 82, 319 (2016)
- Li ZJ, Zhong J, Liu MC, Rong JC, Yang K, Zhou JY, Shen L, Gao F, He HF, Chin. J. Polym. Sci., 38, 932 (2020)
- Louage B, Zhang QL, Vanparijs N, Voorhaar L, Vande Casteele S, Shi Y, Hennink WE, Van Bocxlaer J, Hoogenboom R, De Geest BG, Biomacromolecules, 16(1), 336 (2015)
- Hashimoto T, Meiji H, Urushisaki M, Sakaguchi T, Kawabe K, Tsuchida C, Kondo K, J. Polym. Sci. A: Polym. Chem., 50(17), 3674 (2012)
- Yamaguchi A, Hashimoto T, Kakichi Y, Urushisaki M, Sakaguchi T, Kawabe K, Kondo K, Iyo H, J. Polym. Sci. A: Polym. Chem., 53(8), 1052 (2015)
- Shen Y, Xu N, Adraro YA, Wang B, Liu Y, Yuan W, Xu X, Huang Y, Hu Z, ACS Sustain. Chem. Eng., 8, 1943 (2020)
- Mo R, Song L, Hu J, Sheng X, Zhang X, Polym. Chem., 11, 974 (2020)
- Montarnal D, Capelot M, Tournilhac F, Leibler L, Science, 334(6058), 965 (2011)
- Yue L, Bonab VS, Yuan D, Patel A, Karimkhani V, Manas-Zloczower I, Global Challenges, 3, 180007 (2019)
- Kuang X, Liu GM, Dong X, Liu XG, Xu JJ, Wang DJ, J. Polym. Sci. A: Polym. Chem., 53(18), 2094 (2015)
- Zolghadr M, Shakeri A, Zohuriaan-Mehr MJ, Salimi A, J. Appl. Polym. Sci., 136, 48015 (2019)
- Garcia JM, Jones GO, Virwani K, McCloskey BD, Boday DJ, ter Huurne GM, Horn HW, Coady DJ, Bintaleb AM, Alabdulrahman AMS, Alsewailem F, Almegren HAA, Hedrick JL, Science, 344(6185), 732 (2014)
- Yuan Y, Sun Y, Yan S, Zhao J, Liu S, Zhang M, Zheng X, Jia L, Nat. Commun., 8, 14657 (2017)
- Smolin EM, Rapoport L, in s-Triazines and Derivatives, Interscience Publishers Inc., New York, pp.533 1959.
- You S, Ma S, Dai J, Jia Z, Liu X, Zhu J, ACS Sustain. Chem. Eng., 5, 4683 (2017)
- Xu Z, Liang Y, Ma X, Chen S, Yu C, Wang Y, Zhang D, Miao M, Nat. Sustain., 3, 29 (2020)
- Zhang C, Leng Y, Jiang P, Li J, Du S, ChemistrySelect, 2, 5469
- Mao Z, Li Z, Hu C, Liu Y, Cao Z, Chen Z, J. Chromatogr. A, 1621, 461031 (2020)
- Kong LZ, Pan CY, Polymer, 49(16), 3450 (2008)
- Kang HG, Lee MS, Sim WJ, Yang TH, Shin KH, Shul YG, Choi YW, J. Membr. Sci., 460, 178 (2014)
- Lewis DM, Ho YC, Dyes Pigment., 28, 171 (1995)
- Wang D, Zheng ZJ, Hong CY, Liu Y, Pan CY, J. Polym. Sci. A: Polym. Chem., 44(21), 6226 (2006)
- Huang ZB, Kang TJ, Chang SH, New J. Chem., 29, 1616 (2005)
- Rim C, Lahey LJ, Patel VG, Zhang H, Son DY, Tetrahedron Lett., 50, 745 (2009)
- Kumar V, Zamora-Olivares D, Anslyn EV, Supramol. Chem., 28, 29 (2016)
- Yoshioka-Tarver M, Condon BD, Cintron MS, Chang SC, Easson MW, Fortier CA, Madison CA, Bland JM, Nguyen TMD, Ind. Eng. Chem. Res., 51(34), 11031 (2012)
- Ranu BC, Banerjee S, Tetrahedron Lett., 48, 141 (2007)