2017
DOI: 10.1016/j.dyepig.2017.06.031
|View full text |Cite
|
Sign up to set email alerts
|

Photodegradation mechanisms and kinetics of Eosin-Y in oxic and anoxic conditions

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

6
85
0

Year Published

2018
2018
2024
2024

Publication Types

Select...
8

Relationship

3
5

Authors

Journals

citations
Cited by 75 publications
(91 citation statements)
references
References 35 publications
6
85
0
Order By: Relevance
“…45380 are compared favorably with those reported in the literature (19). Moreover, in accordance with previous studies (19,20), no peaks traceable to the light-induced decomposition of C.I. 45380 were observed under the HPLC conditions used, which indicated that the photoproducts absorbed at different wavelengths and exhibited different chromatographic retention as compared to the parent dye compound.…”
Section: Photodegradation Studiessupporting
confidence: 92%
“…45380 are compared favorably with those reported in the literature (19). Moreover, in accordance with previous studies (19,20), no peaks traceable to the light-induced decomposition of C.I. 45380 were observed under the HPLC conditions used, which indicated that the photoproducts absorbed at different wavelengths and exhibited different chromatographic retention as compared to the parent dye compound.…”
Section: Photodegradation Studiessupporting
confidence: 92%
“…Eosin was discovered in 1873 by Henry Caro by the bromination of fluorescein and it was commercialized as a textile dye in the same year (Geldof ). When precipitated with aluminum, lead or potassium salts, the soluble Eosin‐Y is converted to an insoluble form, named geranium lake, and is widely used as a red pigment in ancient Western artefacts (Alvarez‐Martin ).…”
Section: Resultsmentioning
confidence: 99%
“…ascribed to the initial red color of EY's chromophore. The shoulder peak at 485 nm shows the dimeric substance of EY and the less intense peak at 259 nm corresponds to the π → π * transitions in the aromatic rings [47]. As can be observed from UV bands during the dye degradation process, the UV absorption bands at λ = 516 nm and 485 nm in the visible region gradually decrease and become invisible after 20 min, indicating the chromophoric part of the molecules has been destructed.…”
Section: Electrocatalytic Performancementioning
confidence: 89%
“…Eosin Y (EY), also named as Acid Red 87, is a xanthene red dye that defined as a conjugated π system [47]. The EY dye is broadly used in dyeing, printing, leather, and fluorescent pigment, and painting industries because of its low prices and bright color.…”
Section: Accepted Manuscriptmentioning
confidence: 99%