Back to results list
Please use this identifier to cite or link to this item:
|Title:||The photocatalytic degradation of alachlor and dicamba in TiO₂suspension||Authors:||Wong, Chi-chung||Keywords:||Hong Kong Polytechnic University -- Dissertations
Water -- Purification -- Photocatalysis
Air -- Purification -- Photocatalysis
|Issue Date:||2003||Publisher:||The Hong Kong Polytechnic University||Abstract:||Direct photolysis and photocatalytic degradations of two widely used herbicides: alachlor and dicamba were studied using three different monochromatic UV lamps (254 nm, 300 nm and 350 nm). The photocatalytic reactions were studied under various conditions including the examination of the effects of different TiO₂ sources, TiO₂ dosages, initial pH and proton sources. The influence of the addition of hydrogen peroxide in photocatalysis of alachlor and dicamba was also investigated using the UV at 300 and 350 nm. Degradation mechanisms of alachlor were studied through intermediates identification. Both the direct photolysis and photocatalytic degradations of alachlor and dicamba follow pseudo first-order decay kinetics. Direct photolysis was a rather slow process, but the rate constants for alachlor photocatalysis were increased by about 11 and 26 times at 300 and 350 nm respectively, whereas the rate constants for dicamba photocatalysis were increased by about 3 and 5 times. TiO₂-P25 was found to be an effective photocatalyst compared to TiO₂-BDH. The direct photolysis of alachlor and dicamba was dominant at 254 nm even if TiO₂ was present in the solution. Among the three UV wavelengths used, the highest photocatalysis quantum yield was obtained at 300 nm. The photocatalytic degradation rate of alachlor and dicamba increased with the dosages of TiO₂, but an overdose of TiO₂ would retard the reaction due to light attenuation. Photocatalysis rate of alachlor were slightly enhanced in an alkaline medium, and the different proton sources causing various degrees of rate retardation were due to the presence of the corresponding counter anions. At low to medium pH ranges, photocatalysis rate of dicamba were increased with pH because of the increase of hydroxide ions, but the reaction was gradually retarded at alkaline medium when the effect of charges repulsion was dominant. Rate retardation caused by the presence of the corresponding counter anions was also observed. Photocatalytic degradations of alachlor and dicamba in TiO₂ suspensions with and without the use of hydrogen peroxide were studied using two different monochromatic UV irradiations (300 and 350 nm). The results of H₂O₂ assisted photocatalysis experiments showed that a low H₂O₂ dosage in photocatalysis using UV at 300 nm would enhance the pseudo first order decay rates by 3.3 times for alachlor and 2.4 times for dicamba, but overdose of H₂O₂ will retard the rate because of the expenditure of hydroxyl radicals. However, this process was found impracticable at UV 350 nm due to the absorption characteristic of H₂O₂. In photocatalysis or H₂O₂-assisted photocatalysis of alachlor, a total of thirteen major intermediates were successfully identified using Liquid chromatographyelectrospray ionization-mass spectrometry (LC-ESI-MS) and MS/MS. The major degradation mechanisms of alachlor photocatalysis include dechlorination, dealkylation, hydroxylation, scission of C-O bond, cyclization and N-dealkylation. Bell-shaped evolution profiles of different intermediates were observed. Accordingly, the degradation pathways of alachlor photocatalysis were proposed in relation to the intermediates evolution profiles to successfully illustrate series of degradation steps.||Description:||ix, 82 leaves : ill. ; 30 cm.
PolyU Library Call No.: [THS] LG51 .H577M CSE 2003 Wong
|URI:||http://hdl.handle.net/10397/3082||Rights:||All rights reserved.|
|Appears in Collections:||Thesis|
Show full item record
Files in This Item:
|b17330737_link.htm||For PolyU Users||162 B||HTML||View/Open|
|b17330737_ir.pdf||For All Users (Non-printable)||2.54 MB||Adobe PDF||View/Open|
Citations as of Jun 18, 2018
Citations as of Jun 18, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.