Handbook of Heterogeneous Catalysis 2008
DOI: 10.1002/9783527610044.hetcat0053
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UVVis–NIRandEPRSpectroscopies

Abstract: The sections in this article are Introduction UV – V is– NIR Spectroscopy EPR Spectroscopy Comparison between UV – V is– NIR ( DRS … Show more

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Cited by 7 publications
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“…As shown in the top left insert figure, the peaks of 214, 318 and 368 nm can be assigned to the maximum absorption of acylamino groups, the R bond of ketone groups and the ether bonds in PU, respectively. Peaks at 203 and 230 nm should be ascribed to the maximum absorption E2 bond and the triethylene conjugated structure of benzene rings in EP [39][40][41]. Besides, the absorption band between 470 and 560 nm may be attributed to the conjugated structures between tertiary amine and the benzene rings, which explain the tawny color of cured EP.…”
Section: Uv-vis Absorptionmentioning
confidence: 99%
“…As shown in the top left insert figure, the peaks of 214, 318 and 368 nm can be assigned to the maximum absorption of acylamino groups, the R bond of ketone groups and the ether bonds in PU, respectively. Peaks at 203 and 230 nm should be ascribed to the maximum absorption E2 bond and the triethylene conjugated structure of benzene rings in EP [39][40][41]. Besides, the absorption band between 470 and 560 nm may be attributed to the conjugated structures between tertiary amine and the benzene rings, which explain the tawny color of cured EP.…”
Section: Uv-vis Absorptionmentioning
confidence: 99%