The effects of silver nitrate on the structure and properties of polyurethanes containing pyridyl units

被引:7
作者
Lee, Hsun-Tsing [1 ]
Tsou, Chi-Hui [2 ,3 ]
Jou, Chi-Hsiung [4 ]
Huang, Fu-Chang [5 ]
Wang, Meng-Ling [6 ]
Suen, Maw-Cherng [7 ]
机构
[1] Vanung Univ, Dept Mat Sci & Engn, Taoyuan 32061, Taiwan
[2] Natl Taiwan Univ Sci & Technol, Dept Mat Sci & Engn, Taipei 10607, Taiwan
[3] Chung Yuan Christian Univ, Dept Chem Engn, R&D Ctr Membrane Technol, Jhongli 32023, Taiwan
[4] Oriental Inst Technol, Dept Mat & Text, New Taipei City 32091, Taiwan
[5] Taoyuan Innovat Inst Technol, Dept Civil & Environm Engn, Jhongli 32091, Taiwan
[6] Taoyuan Innovat Inst Technol, Grad Sch Mat Appl Technol, Taoyuan 32091, Taiwan
[7] Taoyuan Innovat Inst Technol, Dept Creat Fash Design, Taoyuan 32091, Taiwan
关键词
Polyurethane; Silver nitrate; 2,6-Pyridinedimethanol; LIQUID-CRYSTALLINE MATERIALS; METAL-COMPLEXES; BENZOIC-ACIDS; CROSS-LINKING; POLYMER; COPOLYMERS; MOIETY; FILMS; INDUCTION;
D O I
10.1007/s00289-014-1222-2
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this study, 2,6-pyridinedimethanol was used as a chain extender to synthesize a new polyurethane, PDM-PU. Further, various amounts of silver nitrate were incorporated to produce PDM-PU/AgNO3 complexes. FT-IR and UV-Vis analyses confirm the formation of complex in the PDM-PU/AgNO3. DSC and DMA results show that the glass transition temperature (T-g), dynamic T-g and storage modulus at 25 degrees C of the PDM-PU/AgNO3 complexes increase with increasing AgNO3 content. This is due to the formation of complex structure that can restrict the segmental motion of polymer chains. The TGA and stress-strain test results show that the thermal decomposition temperature, tensile strength and elongation at break increase with the AgNO3 content initially. Then, they decrease inversely. This indicates that the formation of complex structure raises these properties when the AgNO3 content is below certain value. But as more coordinate bonds were formed, the specimens become brittle. In addition, the crosslink effect caused by coordinate bonds inhibits the dissolution of polymer chains and thereby reduces the swelling degree of the complexes in solvent. Furthermore, AgNO3 imparts antibacterial activity against S. aureus and K. pneumoniae to the complexes
引用
收藏
页码:2749 / 2767
页数:19
相关论文
共 35 条
[1]  
Alaa S, 2014, MACROMOL RAPID COMM, V35, P513
[2]   Chemists look to follow biology lead [J].
Alper, J .
SCIENCE, 2002, 295 (5564) :2396-2397
[3]  
Ambrozic G, 2005, ACTA CHIM SLOV, V52, P207
[4]   Synthesis and Characterization of Poly(methyl methacrylate) Backbone Polymers Containing Side-Chain Pendant Ruthenium(II) Bis-Terpyridine Complexes With an Elongated Conjugated System [J].
Breul, Alexander M. ;
Schafer, Johann ;
Friebe, Christian ;
Schluetter, Florian ;
Paulus, Renzo M. ;
Festag, Grit ;
Hager, Martin D. ;
Winter, Andreas ;
Dietzek, Benjamin ;
Popp, Jurgen ;
Schubert, Ulrich S. .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 2012, 213 (08) :808-819
[5]   Photoluminescence properties of poly [2-(5′-cyano-5′-methyl-hexyloxy)-1,4-phenylene] and its copolymers with pyridine comonomer units [J].
Chang, Jungyun ;
Han, Jungwook ;
An, Jongdeok ;
Im, Chan ;
Yu, Young-Jun ;
Jin, Jung-Il .
JOURNAL OF THE KOREAN PHYSICAL SOCIETY, 2007, 51 (06) :1993-1998
[6]   Novel metal-polyurethane complexes with enhanced antimicrobial activity [J].
Francolini, I ;
Ruggeri, V ;
Martinelli, A ;
D'Ilario, L ;
Piozzi, A .
MACROMOLECULAR RAPID COMMUNICATIONS, 2006, 27 (04) :233-237
[7]  
Huang SL, 1998, J APPL POLYM SCI, V67, P865, DOI 10.1002/(SICI)1097-4628(19980131)67:5<865::AID-APP12>3.3.CO
[8]  
2-8
[9]   Effects of Ca2+ crosslinking on structure and properties of waterborne polyurethane-carboxymethylated guar gum films [J].
Huang, Yihong ;
Yu, Huiqun ;
Xiao, Chaobo .
CARBOHYDRATE POLYMERS, 2006, 66 (04) :500-513
[10]   Hydrogen-bonded polymer complexes of macrocycles containing a pyridyl moiety and carboxyl-functionalized polystyrenes - An approach to H-bonded rotaxanes [J].
Ihata, O ;
Kato, T .
POLYMER BULLETIN, 1999, 42 (05) :497-503