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http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/63000完整後設資料紀錄
| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 劉貴生(Guey-Sheng Liou) | |
| dc.contributor.author | Wen-Chang Wang | en |
| dc.contributor.author | 王文昌 | zh_TW |
| dc.date.accessioned | 2021-06-16T16:18:13Z | - |
| dc.date.available | 2018-03-06 | |
| dc.date.copyright | 2013-03-06 | |
| dc.date.issued | 2013 | |
| dc.date.submitted | 2013-02-04 | |
| dc.identifier.citation | Chapter 1
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| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/63000 | - |
| dc.description.abstract | 本論文分成四個章節，第一張為總體序論。第二章以三苯胺為主體4種二酸酐N,N-bis(3,4-dicarboxyphenyl)aniline dianhydride 、N,N-bis(3,4-dicarboxyphenyl)-1-aminonaphthalene dianhydride 、 N,N-bis(3,4-dicarboxyphenyl)-1-aminopyrene dianhydride及N,N-bis(3,4-dicarboxyphenyl)-2,4,6-trimethylaniline dianhydride被成功的合成出並具有高的純度及好的產率。四系列的聚醯亞胺可由三苯胺為主體的二酸酐與不同的二胺利用一步聚合法合成出。第三章是以相同的N,N-bis(3,4-dicarboxyphenyl)aniline dianhydride, N,N-bis(3,4-dicarboxyphenyl)-1-aminonaphthalene dianhydride, N,N-bis(3,4-dicarboxyphenyl)-1-aminopyrene dianhydride and N,N-bis(3,4-dicarboxyphenyl)-2,4,6-trimethylaniline dianhydride為主體與不同的二胺合成出三個系列之芳香族聚醯胺，可應用在氣體穿透。第四章節為結論。這四個系列三苯胺或二苯胺取代衍生之芳香族高分子之合成與基本特性、光致發光及氣體穿透性質已被研究與比較。所有的高分子在極性非質子型溶劑中有好的溶解性，出色的薄膜成形能力，高的玻璃轉換溫度，好的熱穩定性和機械性質及在薄膜態時高的量子效率。 | zh_TW |
| dc.description.abstract | This study has been separated into four chapters. Chapter 1 is general introduction. Chapter 2 includes four triarylamine-based aromatic dianhydrides, N,N-bis(3,4-dicarboxyphenyl)aniline dianhydride, N,N-bis(3,4-dicarboxyphenyl)-1-aminonaphthalene dianhydride, N,N-bis(3,4-dicarboxyphenyl)-1-aminopyrene dianhydride, and N,N-bis(3,4-dicarboxyphenyl)-2,4,6-trimethylaniline dianhydride synthesizing successfully in high purity and good yields. Four series of polyimides could be readily prepared from the triarylamine-based dianhydride monomers and various diamines via the one step polycondensation. The chapter 3 include four series of aromatic polyimides and derived from N,N-bis(3,4-dicarboxyphenyl)aniline dianhydride, N,N-bis(3,4-dicarboxyphenyl)-1-aminonaphthalene dianhydride, N,N-bis(3,4-dicarboxyphenyl)-1-aminopyrene dianhydride, and N,N-bis(3,4-dicarboxyphenyl)-2,4,6-trimethylaniline dianhydride and various diamine by one step polycondensation. These polyimides could be used in gas separation application. Chapter 4 is conclusions. The synthesis, basic characterization, photoluminescent and gas permeable properties of four series of aromatic triphenylamine (TPA) or diphenylamine (DPA)-substituted derived polymers were investigated and compared. All polymers had good solubility in many polar aprotic solvents, and exhibited excellent thin-film-forming ability. In addition to high Tg values, good thermal stability, mechanical properties, and high luminescence in film state. | en |
| dc.description.provenance | Made available in DSpace on 2021-06-16T16:18:13Z (GMT). No. of bitstreams: 1 ntu-102-R99549002-1.pdf: 5992377 bytes, checksum: 4c7e50972edb9736248a8443ffcd264e (MD5) Previous issue date: 2013 | en |
| dc.description.tableofcontents | Chapter 1
General Introduction 1.1 HIGH PERFORMANCE POLYMERS 2 1.1.1 Preparation of Aromatic Polyimides 3 1.1.2 Modification of Aromatic Polyimides 6 1.2 EVOLUTION OF PHOTOLUMINESCENCE 9 1.3AGGREGATION-INDUCED EMISSION ENHANCEMENT(AIEE) 14 1.4 Electrospining 16 1.4.1 Nanofibers 17 1.4.2 Background of Electrospining 18 1.4.3 Photoluminescent Electrospun Nanofibers 20 1.5 POLYMER MEMBRANE GAS SEPARATION 22 1.5.1 Evolution of Membrane Gas Separation 22 1.5.2 Types of Membranes 24 Porous Membrane 24 Nonporous or Dense Membrane 25 Asymmetric Membrane 25 1.5.3 Mechanisms of Membrane-based Gas Separations 26 Kinetic Diameters 26 1.5.4 Modification of Chemical Structure 28 1.5.5 Robeson Upper Bound Trade-off Line 28 1.5 RESEARCH MOTIVATION 31 REFERENCES AND NOTES 34 Chapter 2 Synthesis and Photoluminescence of High Tg and Organosoluble Novel Aromatic Polyimides Derived from Triarylamine-containing dianhydrides ABSTRACT OF CHAPTER 2 47 2.1 INTRODUCTION 48 2.2 EXPERIMENTAL SECTION 50 2.2.1 Materials 50 2.2.2 Monomer Synthesis 50 N-Methyl 4-bromorophthalimide (1) 50 N,N-Bis (N-Methyl 4-phthalimide)aniline (2) 51 N,N-Bis(3,4-dicarboxyphenyl)aniline Dianhydride (3) 51 N,N-Bis (N-Methyl 4-phthalimide)-1-aminonaphthalene (2’) 52 N,N-Bis(3,4-dicarboxyphenyl)-1-aminonaphthalene Dianhydride (3’) 53 N,N-Bis (N-Methyl 4-phthalimide)-1-aminopyrene (2’’) 54 N,N-Bis(3,4-dicarboxyphenyl)-1-aminopyrene Dianhydride (3’’) 55 N,N-Bis(N'-methyl 4-phthalimide)-2,4,6-trimethylaniline (2’’’) 56 N,N-Bis(3,4-dicarboxyphenyl)-2,4,6-trimethylaniline dianhydride (3’’’) 57 2.2.3 Polymer Synthesis 58 2.2.4 Preparation of the Polyimide Films 59 2.2.5 Fabrication of Electrospun Fibers 59 2.2.6 Measurements 59 2.3.1 Monomer Synthesis 62 2.3.2 Polymer Synthesis 73 2.3.3 Polymer Properties 79 2.3.3.1 Basic Characterization 79 2.3.3.2 Thermal Properties 81 2.3.3.3 Optical Properties 84 2.3.3.4 Aggregation-Induced Emission Enhancement (AIEE) 95 2.3.3.5 Electrochemical Properties 100 REFERENCES AND NOTES 103 Chapter 3 Preparation of Novel Gas-permeable Aromatic Polyimides Derived from Triarylamine-based Dianhydrides ABSTRACT OF CHAPTER 3 107 3.1 INTRODUCTION 108 3.2 EXPERIMENTAL SECTION 110 3.2.1 Materials 110 3.2.2 Polymer Synthesis 110 3.2.3 Preparation of the Polyimide Films 111 3.2.4 Measurements 111 3.3 RESULTS AND DISCUSSION 113 3.3.1 Polymer Synthesis 113 3.3.2 Polymer Properties 117 Basic Characterization 117 Electrochemical Properties 121 Gas Separation 123 3.4 SUMMARY 128 REFERENCES AND NOTES 129 | |
| dc.language.iso | en | |
| dc.title | 含芳香族胺基團功能性芳香族高分子合成及其
光致發光與氣體穿透性質研究 | zh_TW |
| dc.title | Synthesis, Photoluminescence and Gas Permeable Properties of Functional Aromatic Polymers Containing Arylamine Moiety | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 101-1 | |
| dc.description.degree | 碩士 | |
| dc.contributor.oralexamcommittee | 陳燿騰(Yaw-Terng Chern),陳志堅(Jyh-Chien Chen),蕭勝輝(Sheng-Huei Hsiao) | |
| dc.subject.keyword | 三苯胺,二苯胺,聚醯亞胺,光致發光,氣體穿透, | zh_TW |
| dc.subject.keyword | triphenylamine,diphenylamine,polyimide,photoluminescence,gas permeability, | en |
| dc.relation.page | 132 | |
| dc.rights.note | 有償授權 | |
| dc.date.accepted | 2013-02-04 | |
| dc.contributor.author-college | 工學院 | zh_TW |
| dc.contributor.author-dept | 高分子科學與工程學研究所 | zh_TW |
| 顯示於系所單位： | 高分子科學與工程學研究所 | |
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