scholarly journals TiO2 Photocatalysis of the Organophosphorus Fenamiphos: Insight into the Degradation Mechanism

2013 ◽  
Vol 2013 ◽  
pp. 1-8
Author(s):  
H. Mountacer ◽  
S. M. Nemmaoui ◽  
S. Rafqah ◽  
G. Voyard ◽  
M. Sarakha

The photocatalytic degradation of the organophosphorus fenamiphos (FN) was studied using titanium dioxide as a photocatalyst and 365 nm as an excitation wavelength. Under our experimental conditions and in aerated solutions, the irradiation in the presence of TiO2 P25 (1.0 g L−1) permitted the evaluation of the half lifetime to 9.5 minutes. Laser flash photolysis experiments showed the formation of an initial species owing to the attack of the hydroxyl radical on FN. It was identified as the adduct OH•-FN. The second order rate constant for its formation was evaluated to 7.3×109 moL−1 L s−1. All the products are formed via the formation of such transient intermediate. They were identified by means of HPLC/MS using electrospray in positive mode (ESI+). Two main processes are responsible for FN photocatalytic transformation: (i) hydroxylation on the aromatic structure and (ii) the scission of the C–O bond. A mechanistic scheme was proposed for the photocatalytic process of FN using titanium dioxide. An efficient mineralization was observed within 24 hours by using a suntest setup.

1988 ◽  
Vol 17 (2) ◽  
pp. 357-360 ◽  
Author(s):  
Hiroaki Misawa ◽  
Ken Sawabe ◽  
Shigeru Takahara ◽  
Hirochika Sakuragi ◽  
Katsumi Tokumaru

1990 ◽  
Vol 10 (5-6) ◽  
pp. 267-275 ◽  
Author(s):  
R. Bonneau ◽  
M. T. H. Liu ◽  
R. Subramanian ◽  
B. Linkletter ◽  
I. D. R. Stevens

The UV absorption spectrum of benzylchlorocarbene, generated by laser flash photolysis of 3-chloro-3- benzyldiazirine, has been observed in the 290-330 nm range. The lifetime of this species, 18 ns at 25°C, is determined by the rate of the 1,2-H migration to produce chlorostyrenes. Quenching rate constants of this carbene by acetic acid and tetramethylethylene have been measured. Comparison of this kinetic data with the quantitative analysis of the products obtained under continuous irradiation gives further insight into the mechanisms of carbene-acetic acid reactions.


2020 ◽  
Author(s):  
Leandro Scorsin ◽  
Leticia Martins ◽  
Haidi Fiedler ◽  
Faruk Nome ◽  
RENE NOME

In the present work, we study the transient laser-induced formation of 4-nitrophenolate (4-NPO<sup>-</sup>) in the ground electronic state and subsequent proton transfer reaction with acetic acid and water with numerical calculations and laser flash photolysis. We employ the Debye-Smoluchowski spherically-symmetric diffusion model of photoacid proton transfer to determine experimental conditions for studying thermally activated chemical reactions in the ground electronic state. Numerically calculated protonation and deprotonation probabilities for 4-NPO<sup>-</sup> and 4-nitrophenol (4-NPOH) in both ground and excited states showed the feasibility of efficiently producing the ground state anion in the photoacid cycle. We performed laser flash photolysis measurements of 4-NPOH to characterize the photo-initiated ground state protonation and deprotonation rate constants of 4-NPO<sup>-</sup>/4-NPOH as a function of acetic acid, pH, temperature and viscosity. Overall, the work presented here shows a simple way to study fast competing bimolecular proton transfer reactions in non-equilibrium conditions in the ground electronic state <i>(GSPT)</i>.


2014 ◽  
Vol 136 (4) ◽  
pp. 1260-1263 ◽  
Author(s):  
Claudio Saracini ◽  
Dimitrios G. Liakos ◽  
Jhon E. Zapata Rivera ◽  
Frank Neese ◽  
Gerald J. Meyer ◽  
...  

2020 ◽  
Author(s):  
Leandro Scorsin ◽  
Leticia Martins ◽  
Haidi Fiedler ◽  
Faruk Nome ◽  
RENE NOME

In the present work, we study the transient laser-induced formation of 4-nitrophenolate (4-NPO<sup>-</sup>) in the ground electronic state and subsequent proton transfer reaction with acetic acid and water with numerical calculations and laser flash photolysis. We employ the Debye-Smoluchowski spherically-symmetric diffusion model of photoacid proton transfer to determine experimental conditions for studying thermally activated chemical reactions in the ground electronic state. Numerically calculated protonation and deprotonation probabilities for 4-NPO<sup>-</sup> and 4-nitrophenol (4-NPOH) in both ground and excited states showed the feasibility of efficiently producing the ground state anion in the photoacid cycle. We performed laser flash photolysis measurements of 4-NPOH to characterize the photo-initiated ground state protonation and deprotonation rate constants of 4-NPO<sup>-</sup>/4-NPOH as a function of acetic acid, pH, temperature and viscosity. Overall, the work presented here shows a simple way to study fast competing bimolecular proton transfer reactions in non-equilibrium conditions in the ground electronic state <i>(GSPT)</i>.


2002 ◽  
Vol 76 (5) ◽  
pp. 480 ◽  
Author(s):  
Xavier Damoiseau ◽  
Francis Tfibel ◽  
Maryse Hoebeke ◽  
Marie-Pierre Fontaine-Aupart

2000 ◽  
Vol 72 (4) ◽  
pp. 451 ◽  
Author(s):  
M. Bazin ◽  
F. Bosca ◽  
M. L. Marin ◽  
M. A. Miranda ◽  
L. K. Patterson ◽  
...  

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