The Triazine Herbicides 2008
DOI: 10.1016/b978-044451167-6.50024-6
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Triazine Soil Interactions

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Cited by 25 publications
(25 citation statements)
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References 213 publications
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“…In aqueous solutions, triazines exist in either neutral or protonated form, depending on the pK a of the compound and on the pH of the system. The ring nitrogen atom, located in the 3-position between the electron-rich alkyl-side chains, is the most basic and hence the most likely site of protonation ( Figure 1b) (24). The main degradation reactions of triazine herbicides are dechlorination, dealkylation, and oxidation.…”
mentioning
confidence: 99%
“…In aqueous solutions, triazines exist in either neutral or protonated form, depending on the pK a of the compound and on the pH of the system. The ring nitrogen atom, located in the 3-position between the electron-rich alkyl-side chains, is the most basic and hence the most likely site of protonation ( Figure 1b) (24). The main degradation reactions of triazine herbicides are dechlorination, dealkylation, and oxidation.…”
mentioning
confidence: 99%
“…At pH ¼ 4.0 (pH > pK a ) 99% of TBA was in a neutral (non-protonated) form. TBA is a Table 3 Membrane properties: contact angle, zeta potential, , and specific flux, Lp chlorotriazine of similar structure as atrazine and it will be protonated only in a strongly acidic environment (pH < 2) [26,27]. There is a connection between the dipole moment and permeate flux decline.…”
Section: Effect Of Pesticide Adsorption On the Membrane's Permeate Flmentioning
confidence: 98%
“…However, if water is present, metribuzin tends to interact with water molecules via hydrogen bonding and form hydrophilic complexes, which in turn, facilitate the leaching process. This may explain the relationship between its solubility and leaching potential [81]. Since surfactants can interact with soil, it may compete with metribuzin for available binding sites in soil.…”
Section: Effect Of Non-ionic Surfactant Brij35 On Metribuzin In Leachatementioning
confidence: 99%