跳到主要內容

臺灣博碩士論文加值系統

(44.220.251.236) 您好!臺灣時間:2024/10/11 03:32
字體大小: 字級放大   字級縮小   預設字形  
回查詢結果 :::

詳目顯示

我願授權國圖
: 
twitterline
研究生:陳振宇
研究生(外文):ChengYU Chen
論文名稱:2-HEMA對水性PU樹脂物性影響之探討
論文名稱(外文):The effect of 2-hydroxyethyl methacrylate on the physical property of water soluble PU Resin
指導教授:郭陽明
指導教授(外文):YangMing Kuo
學位類別:碩士
校院名稱:中國文化大學
系所名稱:應用化學研究所
學門:自然科學學門
學類:化學學類
論文種類:學術論文
論文出版年:2006
畢業學年度:94
語文別:中文
論文頁數:70
中文關鍵詞: 異氰酸酯 添加劑 作用力 水溶液 架橋力
外文關鍵詞:puwater-based polyureythane
相關次數:
  • 被引用被引用:0
  • 點閱點閱:865
  • 評分評分:
  • 下載下載:0
  • 收藏至我的研究室書目清單書目收藏:1
甲苯二異氰酸酯與聚酯,2-hydroxyethyl methacrylate及其他添加劑反應成水性PU樹脂之分子結構己經IR光譜證實,實驗數據顯示水性PU數之分子之平均粒徑會隨2-hydroxyethyl methacrylate濃度之增高而變大,這是因為水性PU數之分子之自由體積變大之故。水性PU樹脂溶液之黏度似乎也會隨著2-hydroxyethyl methacrylate濃度之增高而變大,原因也是因為水性PU樹脂分子之自由體積變大之故。至於水性PU樹脂溶液之表面張力會隨2-hydroxyethyl methacrylate濃度之增高而變大,這是因為水溶液表面上的非極性基排列較整齊之故
水性PU樹脂薄膜之拉硬力會隨2-hydroxyethyl methacrylat濃度增高而略為變大,這是因為水性PU分子與分子間的作用力增強,而使得水性PU樹脂分子的架橋力增強之故。不過,水性PU樹脂薄膜之伸長率卻會隨2-hydroxyethyl methacrylat濃度增高而變小,這是因為水性PU樹脂分子本身的作用力增強之故。
The reaction of toluene diisocyanate with polyester, 2-hydroxyethylmethacrylate and other additives to form the structure of water-based polyureythane(PU) resin molecule has been proven by IR spectra. Experimental date showed that the average particle size of the water-based PU resin in water increased with increasing concentration of 2-hydroxyethyl methacrylate. This may be due to the result of increased free volume of the PU resin molecule. In aqueous solution, the viscisty of the water-based PU resin molecule also appeared to increase with an increase of 2-hydroxyethyl methacrylate concentration, as a result of increased free volume of the water-based PU resin molecule. For water-based PU resin in water, the surface tensin was seem to increase with increasing concentration of 2-hydroxyethylmethacrylate. This may be attributed to the hydrophobics effect of the PU resin molecule adsorbed at the surface of the water becoming even more ordered.
The tensile strength of the film made by the water-based PU resin slightly increased with increcsing concentration of 2-hydroxyethylmethacrylate. This may be due to increased crosslinking capability resulting from intermolecular interaction between water-based PU resin molecules themselves and between PU molecule and water molecule. On the other hand, however, the elongation of the file made by the water-based PU resin decreased with increasing concentration of 2-hydroxyethylmethacrylate, as a result of strong intramolecular interaction of the PU resin molecule itself.
目 錄
謝誌
中文摘要--------------------------------------------------i
英文摘要-------------------------------------------------ii
第一章 前言-----------------------------------------------1
第二章 理論部份-------------------------------------------3
2.1 PU離子體----------------------------------------------4
2.1-1 PU離子體的合成反應----------------------------------6
2.2 原料--------------------------------------------------8
2-2-1 異氰酸酯(Isocyanate)------------------------------8
2.2-2 多元醇(Polyol)-----------------------------------15
2.2-3 鏈延長劑(linkage extender)-------------------------16
2.2-4 催化劑(catalyst)-----------------------------------17
2.2-5 內部乳化劑(Intrnal emulsifiers)--------------------19
2.2-6 架橋劑(Cross-linking Agent)------------------------20
2.2-7 溶劑的選擇-----------------------------------------21
2.3 PU離子體的製造---------------------------------------22
2.3-1 溶液法(solution process)---------------------------23
2.3-2 預聚物混合法(prepolymer mixing process)------------23
2.3-3 熱熔法(melt dispersion process)--------------------24
2.3-4 丙酮製程-------------------------------------------27
2.3-5預聚物混合法(prepolymer mixing process)-------------28
2.4 游離基聚合反應---------------------------------------29
2.4-1 開始過程(Initiation)-------------------------------29
2.4-2 生長過程(Growth;Propagation)-----------------------30
2.4-3 終結過程(Termination)------------------------------30
第三章 實驗部份------------------------------------------32
3-1 實驗之分析儀器設備-----------------------------------32
3.1-1 實驗裝置-------------------------------------------32
3.1-2 分析儀器-------------------------------------------33
3.1-3 實驗藥品-------------------------------------------34
3.2 水性PU/2-HEMA樹脂溶液製備---------------------------36
3.2-1水性PU/2-HEMA樹脂乳液之薄膜之製備------------------37
3.3 物性之測試-------------------------------------------38
3.3-1 紅外線光譜儀之測試---------------------------------38
3.3-2 表面張力之測試(Wilhelmy法)-------------------------39
3.3-3 黏度之測試-----------------------------------------40
3.3-4 機械性質之測試-------------------------------------41
3.3-5 平均粒徑及擴散係數之測試---------------------------43
第四章 結果與討論----------------------------------------45
4.1 IR光譜探討-------------------------------------------45
4.2 物性之探討-------------------------------------------49
4.2-1 平均粒徑(Number Average Particle)之探討------------49
4.2-2 表面張力(surface Tension)之探討--------------------57
4.2-3 黏度(Viscosity)之探討------------------------------59
4.2-4 拉應力(Tensile strength)之探討---------------------61
4.2-5 伸長率(Elongation)之探討---------------------------65
第五章 結論----------------------------------------------67
第六章 參考文獻------------------------------------------68








圖 目 錄
圖一 The urethane link-------------------------------------3
圖二 分子結構與PU之關係圖---------------------------------3
圖三 離子體結構圖-----------------------------------------4
圖四 PU結構以X-ray繞射和熱分析結果顯示--------------------5
圖五 PU樹脂海島狀結晶相-----------------------------------5
圖六 陽離子型PU離子體之製程反應---------------------------6
圖七 羧酸型PU陰離子體之製程反應---------------------------7
圖八 磺酸型PU離子體之製程反應-----------------------------7
圖九 芳香族及脂肪族異氰酸鹽-------------------------------9
圖十 內部乳化劑種類--------------------------------------19
圖十一 溶液法之製程--------------------------------------23
圖十二 預聚合物混合法之製程------------------------------24
圖十三 熱熔法之製----------------------------------------25
圖十四 丙 酮 製 程---------------------------------------27
圖十五 預聚合物混合攪拌製程------------------------------28
圖十六 實驗裝置圖----------------------------------------32
圖十七 IR spectrum of Toluene diisocyanate (TDI) at 25±0.05℃
--------------------------------------------------46
圖十八 IR spectrum of 2-hydroxyethylmethacrylate (2-HEMA) at
25±0.05℃-----------------------------------------47
圖十九 IR spectrum of Toluene diisocyanate (TDI) and
3-Glycidoxpropyltrimethoxysilane (S510) in PU at
25±0.05℃-----------------------------------------48
圖二十 Plot number average particle size of the PU ionomer
versus the concentration of2-hydroxyethylmethacrylate
,at 25±0.05℃-------------------------------------50
圖二十一 Plot of the intensity versus the diameter of the PU
ionomer molecule (45.78) at 25±0.05℃-------------51
圖二十二 Plot of the intensity versus the diameter of the PU
ionomer molecule (61.31) at 25±0.05℃-------------52
圖二十三 Plot of the intensity versus the diameter of the PU
ionomer molecule (56.93) at 25±0.05℃-------------53
圖二十四 Plot of the intensity versus the diameter of the PU
ionomer molecule (69.85) at 25±0.05℃-------------54
圖二十五 Plot of the intensity versus the diameter of the PU
ionomer molecule (78.55) at 25±0.05℃-------------55
圖二十六 Plot of the intensity versus the diameter of the PU
ionomer molecule (66.37) at 25±0.05℃-------------56
圖二十七 Plot of the surface tension versus the concentration
of 2-hydroxyethylmethacrylate used to make the PU
ionomer, at 25±0.05℃----------------------------58
圖二十八 Plot of the viscosity versus the concentration of
2-hydroxyethylmethacrylate used to make the PU
ionomer, at 25±0.05 ℃---------------------------60
圖二十九 Plot of the modulus (100%) versus the concentration
of 2-hydroxyethylmethacrylate used to make the PU
ionomer,at 25±0.05℃----------------------------62
圖三十 lot of the modulus (200%) versus the concentration of
2-hydroxyethylmethacrylate used to make the PU
ionomer,at 25±0.05℃------------------------------63
圖三十一 Plot of the tensile strength versus the concentration
of 2-hydroxyethylmethacrylate used to make the PU
ionomer,at 25±0.05℃----------------------------64
圖三十二 Plot of the elongation versus the concentration of
2-hydroxyethylmethacrylate used to make the PU
ionomer,at 25±0.05℃----------------------------66
表 目 錄
表一 異氰酸鹽的黃變情形----------------------------------11
表二 異氰酸鹽與CH3OCH2CH2OH反應性-------------------------12
表三 TDI物理性質-----------------------------------------14
表四 催化劑對於Diisocyanate反應催化效果-----------------18
表五 DMAC的物性------------------------------------------22
表六 紅外線光譜特性吸收峰頻率----------------------------38
參考文獻
1. C.L.Wang, D.Y.Chao, J.Appl.Polym.Sci., 78, 1932(2000).
2. D.J.David,H.B.Staley,“Analytical Chemistry of the
polurethanes”, High polymers, VolXVI, PartIII,P.34(1969).
3. Pretsch,T.Clerc,J.Seibl,W.Simon,“Structure Determinatio
n of Organ-ic Compounds”,2nd edition,Springer Verlag(1989).
4. F.G.Saalfied, M. Y. McDowell, Mass spectrometric Metho
for the Determination of Permeability Coefficients ; Report
NRL 6182 ; U.S. Naval Research Laboratory, Washington D.C
1964.
5. F.J.Norton, Diffusion of Helium and Xenon through polymers;Report KAPL 737 ; Knolls Atomic Power Laboratory
(General Electric Co.), New York, 1952.
6. K.O. Ziegel, J. Macromol. Sci.phys. 5, 1122(1971).
7. K.H.H.Y.C.Chiang,“Interpenetrating polymer of polyurethane resi-n”,Angewande Makromolekulare Chemie,193,(1991).
8. T.A.Time,K.M.Mukhina,E.A.Sidorovich and T.S.Dmitrieva“I
nter P-olymer Science and Technology”,Vol.19,No.11(1992).
9. J.B.Clarke,“Additives for Water-Bawed Catings”,P.P Co
lour Jour-nal1881(4290),1991.
10. Gunter Oertel,“polyurethane Handbook”,Garl Hanser Ve
rlag,Muenchen,(1985).
11. D.Y.Chao,“The Role of Surfactants in Synthesizing Poly
urea M-icrocapsule”,Journal of Applied Polymer Science,
Vol.47, 645-651(1993).
12. K.H.HY.C.Chiang,“Interpenetrating Polymer net of polyurethame and epoxy resin,I”,Die Angewande Makromolekulare Chemie,1- 93, (1991).
13. U.S.Patent2, 921,877(1960).
14. Goentre Oertel,”Polyurethane Handbook’’, Garl Hanse
r Verlag, Muenchen, P.24(1985).
15. J.W.Rosthauser,K.Nachtkamp,In:Asvances in Urethane
Science a- nd Technology, Vol 10,P.121(1987).
16. U.S.Patent4, 190566(1980).
17. O.Lorenz, V.B-uddeandk.-H.Reinmoeller, Angew.Makromol,
Chen 87, 35(1980).
18. O.Lorenz, H.Hick, Angew.Makromol.Chem., 72,115(1978).
19. D.Y.Chao,”On the study of chain conformation of Water-
Base Polyureane”, 6th International Conference on Surface
and Colloid science, Hakone, Japan, June, 1988;界面科學會
誌,第十二卷第二期(1988).
20. 聚丙烯/改質聚醯胺、聚丙烯/改質聚醯胺奈米尼龍黏土及聚
丙烯/改質聚醯胺乙烯乙烯醇共聚合物汽油阻隔性能之研究戎
家宏 碩士論文 民93
21. 奈米二氧化矽改質負型壓克力光阻之製備 林秉毅 碩士論文 民93
22. 新型螢光染料水性PU樹脂之合成及其物性之研究 黃鴻麟
碩士論文 民91
23. 何經,呂佳燕,黃勝明 ”高分子材料”, p38-40 復文書局(1990).
24. 林尚安,陸耘“高分子化學”, p.120 高立圖書公司(1998).
25.李德育,顏文義,莊祖煌等編著”聚合物物性”, P.202-211,高 立圖書公司(1988).
26.林建中編著,”高分子化學原理”, P.30-35, 歐亞書局有限公 司(1987).
27.薛敬和主譯”高分子化學”, P.444-457, 高立圖書公司(1989).
28.陳劉旺,丁金超編著,”高分子加工”, P.31-36, 高立圖書公 司(1989).
29. 陳壽安、胡 德、金惟國,” 高分子物性”P.45-46,高立圖書公 司(1987).
30. 李育德、張榮語、馬振基” 高分子加工”P.32-36,高立圖書公司(1988).

參考綱址:
網址:http://www.chemnet.com.tw
網址:http://nanost.ntu.edu.tw/device_manual/HYC026600.pdf
QRCODE
 
 
 
 
 
                                                                                                                                                                                                                                                                                                                                                                                                               
第一頁 上一頁 下一頁 最後一頁 top