Factors influencing the photofading of commercial anthraquinone dyes in solution |
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Authors: | Norman S. Allen Kenneth O. Fatinikun A.Keith Davies Barry J. Parsons Glyn O. Phillips |
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Affiliation: | Department of Chemistry, John Dalton Faculty of Technology, Manchester Polytechnic, Chester Street, Manchester M1 5GD, Great Britain;Department of Biochemistry, University of Salford, Salford M5 4WT, Lancs., Great Britain;School of Natural Sciences, Kelsterton College, N.E. Wales Institute, Connahs Quay, Clwydd, N. Wales, Great Britain |
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Abstract: | The photofading of two anthraquinone dyes has been studied in aqueous solution using ultraviolet-visible absorption spectroscopy and flash photolysis. The influence of alcohol concentration, pH, atmosphere, photosensitisers and stabilisers have been examined and these lead to some important conclusions on the mechanism of dye fading. Essentially, the results indicate the photoexcited triplet state of the dye undergoes a process of either electron or hydrogen-atom abstraction depending on the nature of the environment. Other factors such as aggregation and singlet oxygen also appear to play an important role in solution photofading. The relevance of these results to photofading in a polymeric phase is discussed. |
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