2001
DOI: 10.1016/s0045-6535(00)00379-9
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Quantum yield study of the photodegradation of hydrophobic dyes in the presence of acetone sensitizer

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Cited by 34 publications
(15 citation statements)
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“…Therefore, the dye structure becomes chemically stable at high pH ranges. The chromophores of the dye remain intact after light irradiation and hence reduce the degradation rate of the dye (Tsui and Chu 2001). Hence, the changes in the behavior of the dye molecule may be responsible for the change in the percentage degradation of dye at higher pH.…”
Section: Effect Of Phmentioning
confidence: 99%
“…Therefore, the dye structure becomes chemically stable at high pH ranges. The chromophores of the dye remain intact after light irradiation and hence reduce the degradation rate of the dye (Tsui and Chu 2001). Hence, the changes in the behavior of the dye molecule may be responsible for the change in the percentage degradation of dye at higher pH.…”
Section: Effect Of Phmentioning
confidence: 99%
“…The quantum yield is a useful parameter indicating the efficiency of a photooxidation reaction, and is defined as the number of molecules being decomposed per photon absorbed [17]: ϕ = number of molecules reacted (or produced) number of photons of light absorbed (16) The quantum yield of BY2 degradation can be calculated from the observed first-order degradation rate constant where a specific form of quantum yield, ϕ based on first-order kinetics was indicated in the following [18]:…”
Section: Comparison Of the Quantum Yield For Both Direct Photolysis Amentioning
confidence: 99%
“…The photochemical reduction of A1 in the acetonitrile-alcohol mixtures is enhanced on addition of benzophenone (<1 mM), acetophenone (5 mM) or acetone (0.3 M). It should be noted that the quantum yield of reduction of A1 in acetone-water (1:1, vol) is U d = 0.06 at pH 3-11 [26]. The observed U H 2 values under sensitized conditions (Table 4) are much larger and only little smaller than unity, the maximum attainable value.…”
Section: Photoreduction Of Amino(methyl)aqsmentioning
confidence: 81%
“…The low reactivity of aminoAQs is ascribed to a charge transfer process, leading to fast deactivation into the ground state. The photoprocesses of aminoAQs have been extensively studied [4,[18][19][20][21], but concerning the reactions of nitroAQs only little is known [22][23][24][25][26].…”
Section: Introductionmentioning
confidence: 99%