1 D), 4-chloro-2-15 methylphenoxy)acetic acid (MCPA), 4-(2,4-dichlorophenoxy)butanoic16 acid (2,4-DB),

2 ace and 4-chloro-2-methylphenoxyacetic acid (MCPA) herbicide was studied using density functional the

3 rbicide 4-chloro-2-methylphenoxyacetic acid (MCPA) was revealed.

4              Different surface OH groups and MCPA proton states were used to mimic the strong effects

5          Rate constants of 0.1-1.3 h(-1) for MCPA, 2,4-D, mecoprop, atenolol, and diclofenac, corresp

6  the drug carbamazepine, while the herbicide MCPA (2-methyl-4-chloro-phenoxyacetic acid) and the drug

7 e potential for degradation of the herbicide MCPA in three horizons of an agricultural soil.

8 entate inner-sphere complex with the neutral MCPA molecule were found to be the most energetically st

9 ) compound-specific isotope fractionation of MCPA (4-chloro-2-methylphenoxyacetic acid) and 2,4-D (2,

10                            The incubation of MCPA in the presence of this material yielded an herbici

11 e sharing of the carbonyl oxygen between the MCPA carboxylate group and a singly coordinated surface

12    A two-step mechanism was proposed for the MCPA removal, in which a reversible first-order adsorpti

13            The nature of the products of the MCPA catalytic degradation as well as the reaction condi

14 al topsoil, we also tested the effect of the MCPA concentration on the mineralization kinetics.