研究生: |
林鈺筌 Yu-Cyuan Lin |
---|---|
論文名稱: |
具新穎性之穩定電致變色與多顏色聚醯胺 Electrochromism and Multicolor of Polyamide with Great Novelty |
指導教授: |
陳燿騰
Yaw-Terng Chern |
口試委員: |
蔡大翔
Dah-Shyang Tsai 華沐怡 Mu-Yi Hua |
學位類別: |
碩士 Master |
系所名稱: |
工程學院 - 化學工程系 Department of Chemical Engineering |
論文出版年: | 2016 |
畢業學年度: | 104 |
語文別: | 中文 |
論文頁數: | 96 |
中文關鍵詞: | 電化學 、電致變色 、多顏色 、聚醯胺 、三苯胺 |
外文關鍵詞: | electrochemistry, electrochromism, muticolor, polyamide, triphenylamine |
相關次數: | 點閱:236 下載:1 |
分享至: |
查詢本校圖書館目錄 查詢臺灣博碩士論文知識加值系統 勘誤回報 |
本研究成功合成新的主鏈型多三苯胺電致變色材料,由新的二胺單體分別與不同二酸進行聚縮合反應合成4系列聚醯胺。這些新合成的聚醯胺可溶於大部分有機溶劑,例如N-methyl-2-prrolidinone(NMP)與N,N-dimethyl-acetamide(DMAC)等。此外這些聚醯胺具有好的熱穩定性,軟化溫度介於203~217℃之間,在空氣與氮氣下的10% 熱重量損失皆高於400℃,且在800℃的殘餘率超過53%以上。這些聚醯胺呈現非常好的電致變色特性,以4b為例,在第一階氧化態,有高的對比(△T% = 50.4%)與高的著色效率(168 cm2/C) ,在經過30000次的開關測試後,其著色效率只衰減4.5%。4b也呈現多色階的特性,在電壓從0.0 V到1.15 V 間,顏色從中性態的無色依序氧化到不同氧化態呈現綠黃色、黃綠色、森林綠、暗青色及深藍色。
A series of main-chain-type electrochromic novel polyamides 4 based on triphenylamine were synthesized from the polycondensation reaction of new diamine monomer 3 with various commercially available aromatic dicarboxylic acids. All the polyamides were amorphous with good solubility in many organic solvents, such as N-methyl-2- prrolidinone (NMP) and N,N-dimethyl-acetamide (DMAC). These polyamides had good thermal stability, with the softening temperature between 203~217℃, 10% weight-loss temperature in excess 400℃ under nitrogen and air state, and char yield at 800℃ in nitrogen higher than 53%.
All the polyamides exhibited excellent electrochromic properties. For example, the polyamide 4b at the first oxidation stage had high color contrast (△T% = 50.4%) and coloration efficiency (168 cm2/C) in visible region, with excellent electrochemical cycling stability(over 30000 times within 4.5% loss relative to its initial coloration efficiency).The polymer film also showed a multicolor characteristic, when applied a potential ranging from 0.0 to 1.15 V, the color change from colorless neutral state to greenyellow, yellowgreen, forestgreen, darkcyan and darkblue.
1.吳和生、楊鴻銘,化工與材料概論,高立圖書有限公司.
2.吳耀庭、溫俊祥,電子與材料雜誌,26期,p.68.
3.何國川,電變色智慧節能原件開發,國立台灣大學化工所,2003.
4.W. H. Armistead; S. D. Stookey, Science, 1964, 144, 3615.
5.李繼炳、肖雲鵬、肖兵、許友好,石油煉製與化工,2004, 35, 5.
6.陳俊武、曹漢昌,催化裂化工藝及工程,北京:中國石化出版社,1995, 112.
7.J. R. Platt, J. Chem. Phys.,1961, 34, 862.
8.S. K. Deb, Appl. Optics. Supp., 1969, 3, 192.
9.S. K. Deb, US Patent 3, 1970, 521, 941.
10.M. Green, Chem. Ind., 1996, 17, 641.
11.P. M. S. Monk, R. j. Mortimer, D. R. Rosseinsky, VCH, Weinheim, 1995.
12.N. Leventis, Electrochromic devices, in: McGraw-Hill Encyclopedia of Science and Technology, 8th, vol. 6, McGraw-Hill, New Yok, 1997.
13.R. J. Mortimer, Chem. Soc. Rev., 1997, 26, 147.
14.工研院材化所,工業材料雜誌290期,2011.
15.謝育忠,電漿濺鍍電致色變氧化鎳薄膜特性研究與節能評估,中原大學化學工程學系碩士學位論文,2012.
16.L. Michaelis, E. S. Hill, J. Gen. Physiol., 1933, 16, 859.
17.J. S. E. M. Svensson, C. G. Granqvist, Ind. Eng. Chem. Prod. Res. Dev., 1985, 12, 392.
18.B. P. Jelle, G. Hagen, Synth. Mat., 1993, 54, 315.
19.吳嘉元,溶膠凝膠法合成以鉭元素為基礎的全固態電致變色元件,國立中央大學光電科學研究所,p.11.
20.C. Harbordt, Ann. Chem. Pharm., 1862, 123, 287.
21.W. H. Carothers, US Pat., 1938, 2, 130, 523.
22.M. Frankel, Y. Liwschitzy, A. Zilkha, J. Am. Chem. Soc., 1953, 75.
23.E. L. Wittbecker, P. W. Morgan, J. Polym. Sci., 1959, 40, 289.
24.P. W. Morgan, S. L. K. Wolek, J. Polym. Sci., 1959, 40, 299.
25.R. G. Beaman, P. W. Morgan, C. R. Kroller, E. L. Wittbeaker, E. E. Magat, J. Polym. Sci., 1959, 40, 39.
26.J. R. Schaetgen, F. H. Koonntz, R. F. Tietz, J. Polym. Sci., 1959, 40, 377.
27.D. J. Lyman, S. L. Jung, J. Polym. Sci., 1959, 40, 407.
28.N. Yamazaki, F. Higashi, J. Kawabata, J. Polym. Sci. Polym. Chem., 1974, 12, 2149.
29.F. D. Hager, Triphenylamine, Org. Syn., 1941, 1, 544.
30.柳霈穎,含三苯胺結構之光致變色凝膠材料之合成及其性質之研究,大同大學化學工程學系化工研究所,2010.
31.H. J. Yen, S. M. Guo, G. S. Liou, J. Polym. Sci. Polym. Chem., 2010, 48, 5271.
32.G. S. Liou, C. W. Chang, S. H. Hsiao, J. Mater. Chem., 2007, 17,1007.
33.G. S. Liou, C. W. Chang, C.W. Chung, Macromolecules, 2008, 41,8441.
34.G. S. Liou, C. W. Chang, Macromolecules, 2008, 41, 1667.
35.S. H. Cheng, S. H. Hsiao, T. H. Su, G. S. Liou, Macromolecules, 2005, 38, 307.
36.S. H. Hsiao, G. S. Liou, H. M. Wang, J. Polym. Sci. Polym. Chem.,2009, 47, 2330.
37.H. J. Yen, G. S. Liou, Chem. Mater., 2009, 21, 4062.
38.G. S. Liou, H. Y. Lin, Macromolecules, 2009, 42, 125.
39.H. J. Yen, H. Y. Lin, G. S. Liou, Chem. Mater., 2011, 23, 1874.
40.S. H. Hsiao, Y. T. Chiu, RSC Adv., 2015, 5, 90941.
41.S. H. Hsiao, H. M. Wang, J. W. Lin, W. Guo, Y. R. Kung, C. M. Leu, T. M. Lee, Mater. Chem. Phys., 2013, 141, 665.
42.H. M. Wang, S. H. Hsiao, J. Polym. Sci., Part A: Polym. Chem., 2014, 52, 272.
43.H. J. Yen, J. H. Wu, W. C. Wang, G. S. Liou, Adv. Opt. Mater., 2013, 1, 668.
44.H. J. Yen, C. J. Chen, G. S. Liou, Chem. Comm., 2013, 49, 630.
45.H. J. Yen, G. S. Liou, J. Polym. Sci. Part A: Polym. Chem., 2009, 47, 1584.
46.J. H. Wu, G. S. Liou, Adv. Funct. Mater.,2014, 24, 6422.
47.H. J. Yen, G. S. Liou, Chem. Commun.,2013, 49, 9797.
48.C. Lambert, G. Nőll, J. Am. Chem. Soc., 1999, 121, 8434.
49.V. Coropceanu, M. Malagoli, J. M. Andre, J. L. Bredas, J. Am. Chem. Soc., 2002, 124, 10519.
50.S. H. Hsiao, C. P. Yang, W. Li. Lin, Macromol. Chem. Phys., 1999, 200, 1428.
51.S. Beaupre, J. Dumas, M. Leclerc, Mater. Chem., 2006, 18, 4011.
52.葉千正,具有高對比、多顏色及低驅動電壓之新型高穩定電致變色聚醯胺材料,國立台灣科技大學化工研究所碩士論文,2011.
53.A. V. Szeghalmi, M. E. Erdmann, V. Engel, M. Schmitt, S. Amyhor, V. Kriegisch, G. Nöll, R. Stahl, C. Lambert, D. Stalke, M. Zabel, J. Popp, J. Am. Chem. Soc., 2004, 126, 7834.