Photodegradation of fragrance materials and triclosan in water: Direct photolysis and photosensitized degradation

Author(s):  
Noriatsu Ozaki ◽  
Tatsunori Tanaka ◽  
Tomonori Kindaichi ◽  
Akiyoshi Ohashi
2021 ◽  
Vol 215 ◽  
pp. 112146
Author(s):  
Marco Picone ◽  
Gabriele Giuseppe Distefano ◽  
Davide Marchetto ◽  
Martina Russo ◽  
Marco Vecchiato ◽  
...  

Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 480
Author(s):  
Valentin Dubois ◽  
Carmen S. D. Rodrigues ◽  
Ana S. P. Alves ◽  
Luis M. Madeira

In the present work, the degradation of p-nitrophenol (PNP) and its mineralization by a UV/Vis-based persulphate activation process was investigated. Firstly, a screening of processes as direct photolysis, persulphate alone and persulphate activated by radiation was performed. The incidence of radiation demonstrated to have an important role in the oxidant activation, allowing to achieve the highest PNP and total organic carbon (TOC) removals. The maximum PNP oxidation (100%) and mineralization (61.6%)—both after 2 h of reaction time—were reached when using T = 70 °C, (S2O82−) = 6.4 g/L and I = 500 W/m2. The influence of radiation type (ultraviolet/visible, visible or simulated solar light) was also evaluated, being found that the source with the highest emission of ultraviolet radiation (UV/visible) allowed to achieve the best oxidation efficiency; however, solar radiation also reached very-good performance. According to quenching experiments, the sulphate radical is key in the activated persulphate oxidation process, but the hydroxyl radical also plays an important role.


Author(s):  
Rafael N. Almeida ◽  
João G.M. Hartz ◽  
Patrícia F. Costa ◽  
Alírio E. Rodrigues ◽  
Rubem M.F. Vargas ◽  
...  

1970 ◽  
Vol 48 (8) ◽  
pp. 1333-1334 ◽  
Author(s):  
B. L. Kalra ◽  
A. R. Knight

The photodecomposition of acetone vapor at 255 °C sensitized by Cd 3P1 atoms has been investigated. On irradiation of the Cd–acetone system at 3261 Å, both direct and sensitized reaction occur. CO and CH4 are the only significant volatile products, and their yield is decreased by addition of SF6 as inert quenching gas. The required participation of triplet acetone molecules in the sensitized reaction and the virtual identity of the direct and sensitized decompositions provide additional evidence for the importance of this excited species in direct photolysis.


1968 ◽  
Vol 46 (4) ◽  
pp. 527-530 ◽  
Author(s):  
N. J. Friswell ◽  
R. A. Back

The Hg(63P1)-sensitized decomposition of HNCO vapor has been briefly studied at 26 °C with HNCO pressures from about 3 to 30 Torr. The products detected were the same as in the direct photolysis, CO, N2, and H2. The quantum yield of CO was appreciably less than unity, compared with a value of 1.5 in the direct photolysis under similar conditions. From this and other observations it is tentatively concluded that a single primary process occurs:[Formula: see text]From a study of the mercury-photosensitized reactions in mixtures of HNCO with H2, it was concluded that hydrogen atoms react with HNCO to form CO but not N2. The initial step is probably addition to form NH2CO. From the competition between reaction [1] and the corresponding quenching by H2, the cross section for reaction [1] was estimated to be 2.3 times that of hydrogen.


1991 ◽  
Vol 39 (12) ◽  
pp. 3168-3169 ◽  
Author(s):  
Kazue OHKURA ◽  
Koh-ichi SEKI ◽  
Masanao TERASHIMA ◽  
Yuichi KANAOKA
Keyword(s):  

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