1999
DOI: 10.1016/s0926-3373(99)00019-3
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Photocatalytic degradation of thiocarbamate herbicide active ingredients in water

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Cited by 69 publications
(39 citation statements)
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“…A brief summary showing the starting material and by-products under photolytic condition is shown below in Chart 2. Konstantinou et al, 2001a;Pelizzetti et al, 1990Pelizzetti et al, , 1992aPelizzetti et al, , 1992bMinero et al, 1996;Muszkat et al, 1995;Sanlaville et al, 1996, Sleiman et al, 2006 Aniline and Amide derivative Amines, Dechlorinated, Dealkylated, Cyclized, Aliphatics, Cyclized Konstantinou et al, 2001bKonstantinou et al, , 2002Sakkas et al, 2004;Peñuela and Barceló, 1996;Pathirana & Maithreepala, 1997 7 Thicarbamate derivative Amine, Carboxy, Sulfoxide, Dealkylated Vidal et al, 1999;Sturini et al, 1996;Vidal & Martin, 2001 8 Phenoxy-acids derivatives Hydroxylated, Carboxylated, Chlorophenols, Quinonidal Herrmann et al, 1998;Topalov et al, 2000;Barbeni et al, 1987;Poulios et al, 1998;9 Organophosphorus derivatives Hydroxy, Oxon, Phenol, Dialkylated, Trialkyl esters, Fragmented products Herrmann, 1999;Konstantinou et al, 2001a, Oncescu et al, 2010Herrmann et al, 1999;Hua et al, 1995;Sakkas et al, 2002;Dominguez et al, 1998 10 Carbamate derivative Hydroxylated, Decarboxylated, Phenolic, Dealkylated, Cyclized Tamimi et al, 2006;Percerancier et al, 1995;Pramauro et al, 1997;Tanaka et al, 1999;Marinas et al, 2001;Bianco Prevot et al, 199...…”
Section: Characterization Of Intermediate Productsmentioning
confidence: 99%
“…A brief summary showing the starting material and by-products under photolytic condition is shown below in Chart 2. Konstantinou et al, 2001a;Pelizzetti et al, 1990Pelizzetti et al, , 1992aPelizzetti et al, , 1992bMinero et al, 1996;Muszkat et al, 1995;Sanlaville et al, 1996, Sleiman et al, 2006 Aniline and Amide derivative Amines, Dechlorinated, Dealkylated, Cyclized, Aliphatics, Cyclized Konstantinou et al, 2001bKonstantinou et al, , 2002Sakkas et al, 2004;Peñuela and Barceló, 1996;Pathirana & Maithreepala, 1997 7 Thicarbamate derivative Amine, Carboxy, Sulfoxide, Dealkylated Vidal et al, 1999;Sturini et al, 1996;Vidal & Martin, 2001 8 Phenoxy-acids derivatives Hydroxylated, Carboxylated, Chlorophenols, Quinonidal Herrmann et al, 1998;Topalov et al, 2000;Barbeni et al, 1987;Poulios et al, 1998;9 Organophosphorus derivatives Hydroxy, Oxon, Phenol, Dialkylated, Trialkyl esters, Fragmented products Herrmann, 1999;Konstantinou et al, 2001a, Oncescu et al, 2010Herrmann et al, 1999;Hua et al, 1995;Sakkas et al, 2002;Dominguez et al, 1998 10 Carbamate derivative Hydroxylated, Decarboxylated, Phenolic, Dealkylated, Cyclized Tamimi et al, 2006;Percerancier et al, 1995;Pramauro et al, 1997;Tanaka et al, 1999;Marinas et al, 2001;Bianco Prevot et al, 199...…”
Section: Characterization Of Intermediate Productsmentioning
confidence: 99%
“…The end products are carbon dioxide, water and inorganic mineral salts. [17][18][19] Homogeneous photochemistry, in general, requires high energy photons and rarely enhances the total degradation of the pollutant. Photocatalytic oxidation using semiconductor materials, such as TiO 2 , has been demonstrated as the effective means for organic degradation in a very short time and with high efficiency.…”
Section: Introductionmentioning
confidence: 99%
“…Cyanuric acid was found to be the common final photoproduct of all herbicides. Triazine-derivatives are considered to be the representatives of pesticides of the most wide-spread practical application; therefore it is of crucial importance to evaluate their fate in the environment (Vidal et al 1999). It was shown that some triazine herbicides undergo photodegradation to form deaminated derivatives (Mansour et al 1993).…”
Section: Introductionmentioning
confidence: 99%