## Abstract Chemiluminescence (CL) from luminol solution and luminol–TiO~2~ suspension after illumination of a 355 nm pulse laser is compared. Both the CL systems showed the CL spectra with maximum wavelength of 430 nm, suggesting that the emission was from the excite state of 3‐aminophthalate ion.
Chemiluminescence from luminol solution after illumination of a 355 nm pulse laser
✍ Scribed by Lingyue Min; Xing-Zheng Wu
- Book ID
- 102760793
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 1023 KB
- Volume
- 24
- Category
- Article
- ISSN
- 1522-7235
- DOI
- 10.1002/bio.1126
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✦ Synopsis
Chemiluminescence (CL) on the time scale of microseconds to milliseconds from luminol solution after illumination of a 355 nm pulse laser is reported. It was found that the CL is the emission from 3-aminophthalate ion (AP*). In CL decay after the pulse laser illumination, a peak was observed from about 200 to 30 μ μ μ μs depending on the laser power and the luminol concentration. It seemed that there was a fast and slow decay process; their kinetics were greatly dependent on the laser power and the luminol concentration. Dissolved oxygen was involved in the CL and played the same role on the whole time scale of microseconds to milliseconds. Involvement of reactive oxygen species such as H 2 O 2 , 1 O 2 , O 2 •-and OH in the CL was examined by adding their scavengers. Experimental results suggested that the possibility of involvement of H 2 O 2 and 1 O 2 in the CL was low. The CL in time periods less than 50 μ μ μ μs might be related to •OH. The • O 2 •--induced CL increased with time after 50 μ μ μ μs and became dominant on the time scale of milliseconds. The CL was considered to be caused by both the photoionization and type I reaction mechanisms.
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