3,4-環氧環己基甲基-3,4-環氧環己基甲酸酯
| 3,4-環氧環己基甲基-3,4-環氧環己基甲酸酯 | |
|---|---|
| |
| 別名 | 7-Oxabicyclo[4.1.0]hept-3-ylmethyl-7-oxabicyclo[4.1.0]heptane-3-carboxylate |
| 識別 | |
| 縮寫 | ECC |
| CAS號 | 2386-87-0 
|
| PubChem | 16949 |
| ChemSpider | 16058 |
| SMILES |
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| 性質 | |
| 化學式 | C14H20O4 |
| 摩爾質量 | 252.31 g·mol−1 |
| 外觀 | Colorless liquid[1] |
| 密度 | 1.17 g·cm−3[1] |
| 熔點 | -37 °C（236 K） |
| 溶解性（水） | Slightly soluble (13.85 g·l−1 (20 °C))[1] |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
3,4-環氧環己基甲基-3,4-環氧環己基甲酸酯（3,4-Epoxycyclohexylmethyl-3',4'-epoxycyclohexane carboxylate，ECC）是一種環脂族環氧樹脂，可用於多種工業用途。它通過陽離子聚合反應，使用熱致光引發劑形成交聯的不溶性熱固性聚合物。眾所周知，基於環脂族環氧樹脂（如 ECC）的配方可通過固化形成具有高耐熱性、耐化學性和良好粘合性的熱固性塑料。[2]
歷史[編輯]
ECC 的均聚是以輻射固化為基礎，通過光化學作用形成超強酸，然後進行陽離子聚合，於20世紀70年代首次實現的。[3]
製造[編輯]
ECC 可通過四氫苯甲醛的季先科反應以及隨後與過酸的環氧化反應製備。[4]
特性[編輯]
反應性[編輯]
在ECC的均聚過程中，需要添加1.5~3 wt%的引發劑。3 wt%以上的引發劑不會進一步加速反應，但引發劑比例的增加會增加所形成的熱固性塑料的脆性。在光聚合之後，通常還需要進行熱後固化，才能完全反應。[5]
這種單體的反應活性低於其可能達到的水平，因為所含的酯基會與活性聚合鏈端發生反應並穩定。因此，它的反應速度明顯慢於其他不含酯基的分子。[2][6]ECC的聚合速度也比自由基單體慢得多。因此，研究的目標是找到聚合速度更快但性能相同的陽離子可聚合單體。[2]
交聯[編輯]
陽離子交聯ECC具有低粘度、優異的電氣性能和高可靠性等特點，可用作絕緣體、鍍膜、粘合劑或印刷油墨，廣泛應用於各種工業領域。[7]然而，均聚ECC極易變脆，要解決這個問題，可以在環氧樹脂基體中加入橡膠或矽樹脂等彈性體顆粒、加入無機填料[8]，或在聚酯多元醇[9]的作用下通過聚合作用進行塑化。聚酯多元醇通過單體活化機制與聚合物網絡共價結合。[10]
參考[編輯]
- ^ 1.0 1.1 1.2 引用錯誤：沒有為名為
GESTIS的參考文獻提供內容 - ^ 2.0 2.1 2.2 2.3 Sasaki, Hiroshi. Curing properties of cycloaliphatic epoxy derivatives. Progress in Organic Coatings. February 2007, 58 (2–3): 227–230. doi:10.1016/j.porgcoat.2006.09.030.
- ^ Crivello, J. V.; Lam, J. H. W. Dye-sensitized photoinitiated cationic polymerization. Journal of Polymer Science: Polymer Chemistry Edition. October 1978, 16 (10): 2441–2451. Bibcode:1978JPoSA..16.2441C. doi:10.1002/pol.1978.170161004.
- ^ Dillman, Brian; Jessop, Julie L. P. Chain transfer agents in cationic photopolymerization of a bis-cycloaliphatic epoxide monomer: Kinetic and physical property effects. Journal of Polymer Science Part A: Polymer Chemistry. 2013-05-01, 51 (9): 2058–2067. Bibcode:2013JPoSA..51.2058D. doi:10.1002/pola.26595.
- ^ Atsushi Udagawa; Yasuhiko Yamamoto; Yoshio Inoue; Riichirô Chûjô. Dynamic mechanical properties of cycloaliphatic epoxy resins cured by ultra-violet- and heat-initiated cationic polymerizations. Polymer. January 1991, 32 (15): 2779–2784. doi:10.1016/0032-3861(91)90108-U.
- ^ Crivello, James V.; Varlemann, Ulrike. Mechanistic study of the reactivity of 3,4-epoxycyclohexylmethyl 3′,4′-epoxycyclohexancarboxylate in photoinitiated cationic polymerizations. Journal of Polymer Science Part A: Polymer Chemistry. October 1995, 33 (14): 2473–2486. doi:10.1002/pola.1995.080331421.
- ^ Cristina Mas; Ana Mantecón; Angels Serra; Xavier Ramis & Josep Maria Salla. Improved thermosets obtained from cycloaliphatic epoxy resins and γ-butyrolactone with lanthanide triflates as initiators. I. Study of curing by differential scanning calorimetry and Fourier transform infrared. Journal of Polymer Science Part A: Polymer Chemistry. 2005-06-01, 43 (11): 2337–2347. Bibcode:2005JPoSA..43.2337M. doi:10.1002/pola.20711.
- ^ Lützen, Hendrik; Bitomsky, Peter; Rezwan, Kurosch; Hartwig, Andreas. Partially crystalline polyols lead to morphology changes and improved mechanical properties of cationically polymerized epoxy resins. European Polymer Journal. January 2013, 49 (1): 167–176. doi:10.1016/j.eurpolymj.2012.10.015.
- ^ Spyrou, Emmanouil. Radiation initiated cationic polymerization with tailor-made polyesters. Progress in Organic Coatings. November 2001, 43 (1–3): 25–31. doi:10.1016/S0300-9440(01)00240-5.
- ^ Yagci, Yusuf; Schnabel, Wolfram. On the mechanism of photoinitiated cationic polymerization in the presence of polyols. Die Angewandte Makromolekulare Chemie. 1999-09-01, 270 (1): 38–41. doi:10.1002/(SICI)1522-9505(19990901)270:1<38::AID-APMC38>3.0.CO;2-S.
相關[編輯]
- Ellis (編). Polymers : a property database 2nd. Boca Raton, Fla.: CRC. 2007: 150. ISBN 978-0-8493-3940-0.