Abiotic Degradation Pathways of Selected Pesticides in the Presence of Oxygen Species in Aqueous Solutions

Author(s):  
A. Mamouni ◽  
M. Mansour ◽  
P. Schmitt
2021 ◽  
Author(s):  
Julie Becher ◽  
Samuel Beal ◽  
Susan Taylor ◽  
Katerina Dontsova ◽  
Dean Wilcox

Two major components of insensitive munition formulations, nitroguanidine (NQ) and 3-nitro-1,2,4-triazol-5-one (NTO), are highly water soluble and therefore likely to photo-transform while in solution in the environment. The ecotoxicities of NQ and NTO solutions are known to increase with UV exposure, but a detailed accounting of aqueous degradation rates, products, and pathways under different exposure wavelengths is currently lacking. We irradiated aqueous solutions of NQ and NTO over a 32-h period at three ultraviolet wavelengths and analyzed their degradation rates and transformation products. NQ was completely degraded by 30 min at 254 nm and by 4 h at 300 nm, but it was only 10% degraded after 32 h at 350 nm. Mass recoveries of NQ and its transformation products were >80% for all three wavelengths. NTO degradation was greatest at 300 nm with 3% remaining after 32 h, followed by 254 nm (7% remaining) and 350 nm (20% remaining). Mass recoveries of NTO and its transformation products were high for the first 8 h but decreased to 22–48% by 32 h. Environmental half-lives of NQ and NTO in pure water were estimated as 4 and 6 days, respectively. We propose photo-degradation pathways for NQ and NTO supported by observed and quantified degradation products and changes in solution pH.


1992 ◽  
Vol 35 (1) ◽  
pp. 13-20 ◽  
Author(s):  
Abderrahim Mamouni ◽  
Philippe Schmitt ◽  
Mohamed Mansour ◽  
Michel Schiavon

Chemosphere ◽  
2003 ◽  
Vol 50 (10) ◽  
pp. 1331-1342 ◽  
Author(s):  
Bent Halling-Sørensen ◽  
Anne Lykkeberg ◽  
Flemming Ingerslev ◽  
Paul Blackwell ◽  
Jette Tjørnelund

PLoS ONE ◽  
2021 ◽  
Vol 16 (10) ◽  
pp. e0258483
Author(s):  
Wenping Dong ◽  
Chuanxi Yang ◽  
Lingli Zhang ◽  
Qiang Su ◽  
Xiaofeng Zou ◽  
...  

This study investigates the degradation of nifedipine (NIF) by using a novel and highly efficient ultraviolet light combined with hydrogen peroxide (UV/H2O2). The degradation rate and degradation kinetics of NIF first increased and then remained constant as the H2O2 dose increased, and the quasi-percolation threshold was an H2O2 dose of 0.378 mmol/L. An increase in the initial pH and divalent anions (SO42- and CO32-) resulted in a linear decrease of NIF (the R2 of the initial pH, SO42- and CO32- was 0.6884, 0.9939 and 0.8589, respectively). The effect of monovalent anions was complex; Cl- and NO3- had opposite effects: low Cl- or high NO3- promoted degradation, and high Cl- or low NO3- inhibited the degradation of NIF. The degradation rate and kinetics constant of NIF via UV/H2O2 were 99.94% and 1.45569 min-1, respectively, and the NIF concentration = 5 mg/L, pH = 7, the H2O2 dose = 0.52 mmol/L, T = 20 ℃ and the reaction time = 5 min. The ·OH was the primary key reactive oxygen species (ROS) and ·O2- was the secondary key ROS. There were 11 intermediate products (P345, P329, P329-2, P315, P301, P274, P271, P241, P200, P181 and P158) and 2 degradation pathways (dehydrogenation of NIF → P345 → P274 and dehydration of NIF → P329 → P315).


2007 ◽  
Vol 81 (4) ◽  
pp. 793-801
Author(s):  
Franco M. Cabrerizo ◽  
Carolina Lorente ◽  
Mariana Vignonl ◽  
Romina Cabrerizo ◽  
Andrés H. Thomas ◽  
...  

2010 ◽  
Vol 88 (6) ◽  
pp. 569-576 ◽  
Author(s):  
Xiaocui Zhao ◽  
Mengni Zhang ◽  
Yitao Long ◽  
Zhifeng Ding

The redox reactions of two main components of reactive oxygen species (ROS), superoxide and hydrogen peroxide, along with oxygen in aqueous solutions were investigated using a conventional electrochemical technique, differential pulse voltammetry (DPV). Superoxide undergoes oxidation at a Pt working electrode biased at 0.055 V versus Ag/AgCl, while hydrogen peroxide can be oxidized and reduced at 0.817 and –0.745 V, respectively. Oxygen in the solutions is reduced at the electrode with an applied potential of –0.455 V. Based on these results, hydrogen peroxide and superoxide released from live cells can be successfully monitored, identified, and mapped using scanning electrochemical microscopy (SECM) at different potentials. Single human bladder (T24) cells were imaged using a 5 μm diameter SECM probe biased at –0.400, –0.600, and –0.800 V. Oxygen reduction that seems an interference can be discriminated from that of hydrogen peroxide by means of SECM.


2006 ◽  
Vol 2006 ◽  
pp. 1-6 ◽  
Author(s):  
Agatino Di Paola ◽  
Maurizio Addamo ◽  
Vincenzo Augugliaro ◽  
Elisa García-López ◽  
Vittorio Loddo ◽  
...  

Aqueous solutions of lincomycin were irradiated with UV light in homogeneous and heterogeneous systems. Lincomycin disappeared in both systems but the presence ofTiO2noticeably accelerated the degradation of the antibiotic in comparison with direct photolysis. The rate of decomposition was dependent on the concentration of lincomycin and followed a pseudo-first-order kinetics. Photolysis involved only the oxidation of lincomycin without mineralization. Differently, the treatment withTiO2and UV light resulted in a complete mineralization of the antibiotic. The degradation pathways involved S- and N-demethylation and propyldealkylation. The mineralization of the molecule led to the formation of sulfate, ammonium, and nitrate ions.


2004 ◽  
Vol 38 (13) ◽  
pp. 3110-3118 ◽  
Author(s):  
Constantinos Vassilakis ◽  
Ariadni Pantidou ◽  
Elefteria Psillakis ◽  
Nicolas Kalogerakis ◽  
Dionissios Mantzavinos

Chemosphere ◽  
2017 ◽  
Vol 166 ◽  
pp. 230-237 ◽  
Author(s):  
Aleix Benito ◽  
Aida Penadés ◽  
Josep Lluis Lliberia ◽  
Rafael Gonzalez-Olmos

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