Microstructure and morphology of amine-cured epoxy coatings before and after outdoor exposures - An AFM study

被引:41
作者
Gu, XH [1 ]
Nguyen, T
Oudina, M
Martin, D
Kidah, B
Jasmin, J
Rezig, A
Sung, LP
Byrd, E
Martin, JW
机构
[1] NIST, Bldg & Fire Res Lab, Gaithersburg, MD 20899 USA
[2] NIST, Ctr Neutron Res, Gaithersburg, MD 20899 USA
[3] Univ Missouri, Kansas City, MO 64110 USA
来源
JCT RESEARCH | 2005年 / 2卷 / 07期
关键词
atomic force microscopy; surface analysis; epoxy resins; durability; physical properties; service life prediction; weatherability; surface chemistry;
D O I
10.1007/s11998-005-0014-x
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Atomic force microscopy (AFM) has been used to study the morphology and microstructure of an amine-cured epoxy before and after outdoor exposure. Measurements were made from samples prepared in an essentially CO2-free, H2O-rree glove box and from samples prepared in ambient conditions. For those prepared in a CO2-free glove box, AFM imaging was conducted on (1) an unexposed air/coating surface, (2) air unexposed coating bulk, (3) an unexposed coating/substrate interface, and (4) a field exposed air/coating surface. For samples prepared in ambient conditions, only the unexposed air/coating surface was investigated. The same regions of the exposed samples were scanned periodically by the AFM to monitor changes in the surface morphology of the coating as UV exposure progressed. Small angle neutron scattering and Fourier transform infrared spectroscopy (FTIR) studies were performed to verify the microstructure and to follow chemical changes during outdoor exposure, respectively. The results have shown that amine blushing, which occurs only under ambient conditions, had a significant effect on the surface morphology and microstructure of the epoxy. The surface morphology of the samples prepared under CO2-free, dry conditions was generally smooth and homogeneous. However, the interface and the bulk samples clearly revealed a two-phase structure consisting of bright nodular domains and dark interstitial regions, indicating an inhomogeneous microstructure. Such heterogeneous structure of the bulk was in good agreement with results obtained by small angle neutron scattering of unexposed samples and by AFM phase imaging of the degraded sample surface. The relationship between submicrometer physical changes and molecular chemical degradation is discussed.
引用
收藏
页码:547 / 556
页数:10
相关论文
共 39 条
[1]   Characterization of the morphologies and nanostructures of blends of poly(styrene) block-poly(ethene-co-but-1-ene)-block-poly(styrene) with isotactic and atactic polypropylenes by tapping-mode atomic force microscopy [J].
Bar, G ;
Thomann, Y ;
Whangbo, MH .
LANGMUIR, 1998, 14 (05) :1219-1226
[2]   STRUCTURE PHOTOOXIDATIVE STABILITY RELATIONSHIP OF AMINE-CROSSLINKED EPOXIES [J].
BELLENGER, V ;
VERDU, J .
POLYMER PHOTOCHEMISTRY, 1984, 5 (1-6) :295-311
[3]   OXIDATIVE SKELETON BREAKING IN EPOXY-AMINE NETWORKS [J].
BELLENGER, V ;
VERDU, J .
JOURNAL OF APPLIED POLYMER SCIENCE, 1985, 30 (01) :363-374
[4]   PHOTOOXIDATION OF EPOXY-RESINS CURED BY NON-AROMATIC AMINES [J].
BELLENGER, V ;
BOUCHARD, C ;
CLAVEIROLLE, P ;
VERDU, J .
POLYMER PHOTOCHEMISTRY, 1981, 1 (01) :69-80
[5]  
BURTON BL, 2001, P EPOX RES FORM M SO
[6]   Chemical and morphological analysis of surface enrichment in a biodegradable polymer blend by phase-detection imaging atomic force microscopy [J].
Chen, X ;
McGurk, SL ;
Davies, MC ;
Roberts, CJ ;
Shakesheff, KM ;
Tendler, SJB ;
Williams, PM ;
Davies, J ;
Dawkes, AC ;
Domb, A .
MACROMOLECULES, 1998, 31 (07) :2278-2283
[7]   Energy dissipation in tapping-mode atomic force microscopy [J].
Cleveland, JP ;
Anczykowski, B ;
Schmid, AE ;
Elings, VB .
APPLIED PHYSICS LETTERS, 1998, 72 (20) :2613-2615
[8]   EPOXY POLYMERS .2. MACROSTRUCTURE [J].
CUTHRELL, RE .
JOURNAL OF APPLIED POLYMER SCIENCE, 1968, 12 (06) :1263-&
[9]   Do epoxy-amine networks become inhomogeneous at the nanometric scale? [J].
Duchet, J ;
Pascault, JP .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2003, 41 (20) :2422-2432
[10]   Are cured thermoset resins inhomogeneous? [J].
Dusek, K .
ANGEWANDTE MAKROMOLEKULARE CHEMIE, 1996, 240 :1-15