Preparation of a self-catalyzed amino-epoxy phthalonitrile resin with a large processing window
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OpenAlex topics: Epoxy Resin Curing Processes · Synthesis and properties of polymers · Fiber-reinforced polymer composites
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References (30)
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1. Ghosh NN, Kiskan B, Yagci Y (2007) Polybenzoxazines—new high performance thermosetting resins: synthesis and properties. Prog Polym Sci 32:1344–1391. https://doi.org/10.1016/j.progpolymsci.2007.07.00210.1016/j.progpolymsci.2007.07.002 ↗
2. Wu M, Xu J, Bai S, Chen X, Yu X, Naito K, Zhang Z, Zhang Q (2020) A high-performance functional phthalonitrile resin with a low melting point and a low dielectric constant. Soft Matter 16:1888–1896. https://doi.org/10.1039/C9SM02328C10.1039/C9SM02328C ↗
3. Derradji M, Ramdani N, Zhang T, Wang J, Lin Z, Yang M, Xu X, Liu W (2015) High thermal and thermomechanical properties obtained by reinforcing a bisphenol-A based phthalonitrile resin with silicon nitride nanoparticles. Mater Lett 149:81–84. https://doi.org/10.1016/j.matlet.2015.02.12210.1016/j.matlet.2015.02.122 ↗
4. Salan Ü, Altindal A, Bulut M, Bekaroğlu Ö (2006) Synthesis, characterization, electrical and dielectric permittivity measurements of 2,9,16,23-tetra(4-ferrocenylimino- 3-nitrophenoxy)phthalocyanines. J Porphyrins Phthalocyanines 10:1263–1270. https://doi.org/10.1142/S108842460600063610.1142/S1088424606000636 ↗
5. Köysal O, Okutan M, San SE, Durmuş M, Ecevit FN, Ahsen V (2007) Diffraction efficiency enhancement caused by employing liquid crystal phthalonitrile derivative in nematic liquid crystals. Dyes Pigm 73:98–102. https://doi.org/10.1016/j.dyepig.2005.10.02010.1016/j.dyepig.2005.10.020 ↗
6. Kahveci B, Özil M, Kantar C, Şaşmaz S, Işık Ş, Köysal Y (2007) Microwave-assisted and conventional synthesis of new phthalocyanines containing 4-(p-fluorophenyl)-3-methyl-4,5-dihydro-1H-1,2,4-triazol-5-one moieties. J Organomet Chem 692:4835–4842. https://doi.org/10.1016/j.jorganchem.2007.06.06710.1016/j.jorganchem.2007.06.067 ↗
7. Chen Y, Ei-Khouly ME, Sasaki M, Araki Y, Ito O (2005) Synthesis of the axially substituted titanium Pc-C60 dyad with a convenient method. Org Lett 7:1613–1616. https://doi.org/10.1021/ol050281l10.1021/ol050281l ↗
8. Guldi DM, Gouloumis A, Vázquez P, Torres T, Georgakilas V, Prato M (2005) Nanoscale organization of a phthalocyanine−fullerene system: remarkable stabilization of charges in photoactive 1-D nanotubules. J Am Chem Soc 127:5811–5813. https://doi.org/10.1021/ja043283u10.1021/ja043283u ↗
9. Hamuryudan E, Merey S, Altuntas Bayir Z (2003) Synthesis of phthalocyanines with tridentate branched bulky and alkylthio groups. Dyes Pigm 59:263–268. https://doi.org/10.1016/S0143-7208(03)00117-710.1016/S0143-7208(03)00117-7 ↗
10. Keller TM, Dominguez DD (2005) High temperature resorcinol-based phthalonitrile polymer. Polymer 46:4614–4618. https://doi.org/10.1016/j.polymer.2005.03.06810.1016/j.polymer.2005.03.068 ↗
11. Laskoski M, Dominguez DD, Keller TM (2005) Synthesis and properties of a bisphenol A based phthalonitrile resin. J Polym Sci A Polym Chem 43:4136–4143. https://doi.org/10.1002/pola.2090110.1002/pola.20901 ↗
12. Peng X, Sheng H, Guo H, Naito K, Yu X, Ding H, Qu X, Zhang Q (2014) Synthesis and properties of a novel high-temperature diphenyl sulfone-based phthalonitrile polymer. High Perform Polym 26:837–845. https://doi.org/10.1177/095400831453247910.1177/0954008314532479 ↗
13. Yu X-Y, Naito K, Kang C, Qu X, Zhang Q (2013) Synthesis and properties of a high-temperature naphthyl-based phthalonitrile polymer. Macromol Chem Phys 214:361–369. https://doi.org/10.1002/macp.20120049210.1002/macp.201200492 ↗
14. Badshah A, Kessler MR, Heng Z, Hasan A (2014) Synthesis and characterization of phthalonitrile resins from ortho-linked aromatic and heterocyclic monomers. Polym Int 63:465–469. https://doi.org/10.1002/pi.452710.1002/pi.4527 ↗
15. Zuo F, Liu X (2010) Synthesis and curing behavior of a novel benzoxazine-based bisphthalonitrile monomer. J Appl Polym Sci 117:1469–1475. https://doi.org/10.1002/app.3197810.1002/app.31978 ↗
16. Laskoski M, Dominguez DD, Keller TM (2013) Alkyne-containing phthalonitrile resins: controlling mechanical properties by selective curing. J Polym Sci Part A: Polym Chem 51:4774–4778. https://doi.org/10.1002/pola.2689910.1002/pola.26899 ↗
17. Xi Z, Chen X, Yu X, Ma Y, Ji P, Naito K, Ding H, Qu X, Zhang Q (2016) Synthesis and properties of a novel high temperature pyridine-containing phthalonitrile polymer. J Polym Sci Part A: Polym Chem 54:3819–3825. https://doi.org/10.1002/pola.2827810.1002/pola.28278 ↗
18. Sheng H, Peng X, Guo H, Yu X, Tang C, Qu X, Zhang Q (2013) Synthesis and thermal properties of a novel high temperature alkyl-center-trisphenolic-based phthalonitrile polymer. Mater Chem Phys 142:740–747. https://doi.org/10.1016/j.matchemphys.2013.08.03310.1016/j.matchemphys.2013.08.033 ↗
19. Sheng H, Zhao F, Yu X, Naito K, Qu X, Zhang Q (2016) Synthesis and thermal properties of high-temperature phthalonitrile polymers based on 1,3,5-triazines. High Perform Polym 28:600–609. https://doi.org/10.1177/095400831559119210.1177/0954008315591192 ↗
20. Dong S, Xu M, Wei J, Yang X, Liu X (2014) The preparation and wide frequency microwave absorbing properties of tri-substituted-bisphthalonitrile/Fe3O4 magnetic hybrid microspheres. J Magn Magn Mater 349:15–20. https://doi.org/10.1016/j.jmmm.2013.08.03810.1016/j.jmmm.2013.08.038 ↗
21. Zhao F, Liu R, Yu X, Naito K, Qu X, Zhang Q (2015) A high temperature polymer of phthalonitrile-substituted phosphazene with low melting point and good thermal stability. J Appl Polym Sci 132:n/a–n/a. doi:https://doi.org/10.1002/app.4260610.1002/app.42606 ↗
22. Lv J, Ma J, Cheng K, Chen C, Hu J, Zeng K, Yang G (2017) Insights into phthalonitrile/epoxy blends modification system from non-competitive cure system based on alicyclic anhydride. Chin J Polym Sci 35:1561–1571. https://doi.org/10.1007/s10118-017-1992-810.1007/s10118-017-1992-8 ↗
23. Zhao X, Lei Y, Zhao R, Liu X (2012) Preparation and thermal properties of flame retardant phthalonitrile/epoxy blends. Sci Eng Compos Mater 19:89–92. https://doi.org/10.1515/secm-2011-012310.1515/secm-2011-0123 ↗
24. Dominguez DD, Keller TM (2008) Phthalonitrile-epoxy blends: cure behavior and copolymer properties. J Appl Polym Sci 110:2504–2515. https://doi.org/10.1002/app.2881710.1002/app.28817 ↗
25. Guo H, Zou Y, Chen Z, Zhang J, Zhan Y, Yang J, Liu X (2012) Effects of self-promoted curing behaviors on properties of phthalonitrile/epoxy copolymer. High Perform Polym 24:571–579. https://doi.org/10.1177/095400831244547810.1177/0954008312445478 ↗
26. Jiang ML, Lei YX, Liu XB (2018) Curing behaviors and properties of epoxy and self-catalyzed phthalonitrile with improved processability. High Perform Polym 30:710–719. https://doi.org/10.1177/095400831771759410.1177/0954008317717594 ↗
27. Augustine D, Vijayalakshmi KP, Sadhana R, Mathew D, Reghunadhan Nair CP (2014) Hydroxyl terminated PEEK-toughened epoxy–amino novolac phthalonitrile blends – synthesis, cure studies and adhesive properties. Polymer 55:6006–6016. https://doi.org/10.1016/j.polymer.2014.09.04210.1016/j.polymer.2014.09.042 ↗
28. Chen X, Liu J, Xi Z, Shan S, Ding H, Qu X, Zhang Q (2017) Synthesis and thermal properties of high temperature phthalonitrile resins cured with self-catalytic amino-contanining phthalonitrle compounds. High Perform Polym 29:1209–1221. https://doi.org/10.1177/095400831667341910.1177/0954008316673419 ↗
29. Zeng K, Zhou K, Zhou S, Hong H, Zhou H, Wang Y, Miao P, Yang G (2009) Studies on self-promoted cure behaviors of hydroxy-containing phthalonitrile model compounds. Eur Polym J 45:1328–1335. https://doi.org/10.1016/j.eurpolymj.2008.12.03610.1016/j.eurpolymj.2008.12.036 ↗
30. Wang J, Hu J, Zeng K, Yang G (2015) Preparation of self-promoted hydroxy-containing phthalonitrile resins by an in situ reaction. RSC Adv 5:105038–105046. https://doi.org/10.1039/C5RA18472J10.1039/C5RA18472J ↗