Startseite The degradation efficiency and mechanism of meclofenamic acid in aqueous solution by UV irradiation
Artikel
Lizenziert
Nicht lizenziert Erfordert eine Authentifizierung

The degradation efficiency and mechanism of meclofenamic acid in aqueous solution by UV irradiation

  • Jian Li , Huihui Zhou , Rong Chen , Tingchao Yu EMAIL logo und Miaomiao Ye EMAIL logo
Veröffentlicht/Copyright: 11. Februar 2017
Veröffentlichen auch Sie bei De Gruyter Brill

Abstract:

The photodegradation of meclofenamic acid (MCFA) was investigated using UV irradiation process. Parameters affecting the photodegradation process such as dissolved oxygen, reaction temperature, solution pH, initial MCFA concentration, humic acid, cations and anions were carried out. The intermediate products were identified by HPLC-MS analysis, and a tentative photodegradation pathway of MCFA was proposed. Results show that the photodegradation of MCFA can be modeled by the first-order kinetics. The photodegradation efficiency increases with the decreased concentration of humic acid or the decreased initial MCFA concentration, while the reaction temperature and the inorganic ions have no significant effect on the MCFA removal. It has found that the optimal initial solution pH for MCFA degradation is about 7.0. Finally, the HPLC-MS results reveal that the Cl atom in the MCFA molecule would form Cl, followed by dechlorination, hydroxylation and cyclization of pentacyclic compounds.

Funding statement: The present work was financially supported by the National Natural Science Foundation of China (No. 51108406), the Zhejiang Provincial Natural Science Foundation of China (No. LY14E080011), the Important National Science and Technology Specific Projects (2012ZX07408-002, 2012ZX07403-004), and the Fundamental Research Funds for the Central Universities (2013QNA4026).

References

1. Daughton CG, Ternes TA. Environ Health Persp. 1999;107(Suppl 6):907–938.10.1289/ehp.99107s6907Suche in Google Scholar

2. Jones O, Voulvoulis N, Lester J. Water Res. 2002;36(20):5013–5022.10.1016/S0043-1354(02)00227-0Suche in Google Scholar

3. Miege C, Choubert J, Ribeiro L, Eusèbe M, Coquery M. Environ Pollut. 2009;157(5):1721–1726.10.1016/j.envpol.2008.11.045Suche in Google Scholar

4. Ratola N, Cincinelli A, Alves A, Katsoyiannis A. J Hazard Mater. 2012;239:1–18.10.1016/j.jhazmat.2012.05.040Suche in Google Scholar

5. Kolpin DW, Furlong ET, Meyer MT, Thurman EM, Zaugg SD, Barber LB,et al. Environ Sci Technol. 2002;36(6):1202–1211.10.1021/es011055jSuche in Google Scholar

6. Ternes TA, Meisenheimer M, McDowell D, Sacher F, Brauch HJ, Haist-Gulde B,et al. Environ Sci Technol. 2002;36(17):3855–3863.10.1021/es015757kSuche in Google Scholar

7. Boyd GR, Reemtsma H, Grimm DA, Mitra S. Sci Total Environ. 2003;311(1):135–149.10.1016/S0048-9697(03)00138-4Suche in Google Scholar

8. Westerhoff P, Yoon Y, Snyder S, Wert E. Environ Sci Technol. 2005;39(17):6649–6663.10.1021/es0484799Suche in Google Scholar PubMed

9. Richter D, Massmann G, Dünnbier U. Chemosphere. 2008;71(8):1574–1581.10.1016/j.chemosphere.2007.11.026Suche in Google Scholar PubMed

10. Kim I, Tanaka H. Environ Int. 2009;35(5):793–802.10.1016/j.envint.2009.01.003Suche in Google Scholar PubMed

11. Samaras V G, Thomaidis N S, Stasinakis A S,et al. Anal Bioanal Chem. 2011;399(7):2549–2561. .10.1007/s00216-010-4607-6Suche in Google Scholar

12. McGurk KA, Remmel RP, Hosagrahara VP, Tosh D, Burchell B. Drug Metab Dispos. 1996;24(8):842–849.Suche in Google Scholar

13. Aronson JK. Meyler’s side effects of analgesics and anti-inflammatory drugs The Netherlands: Elsevier Science, Amsterdam; 2009.Suche in Google Scholar

14. Lees P, Higgins AJ. Equine Veterinary J. 1985;17:83–96. .10.1111/j.2042-3306.1985.tb02056.xSuche in Google Scholar

15. Ye MM, Zhou HH, Zhang TQ. Chem Eng J. 2013;226:209–216.10.1016/j.cej.2013.04.064Suche in Google Scholar

16. Zhang DD, Qiu RL, Song L, Eric B, Mod YQ, Huang XF. J Hazard Mater. 2009;163(2):843–847.10.1016/j.jhazmat.2008.07.036Suche in Google Scholar

17. Doll TE, Frimmel FH. Chemosphere. 2003;52(10):1757–1769.10.1016/S0045-6535(03)00446-6Suche in Google Scholar

18. Vogna D, Marotta R, Napolitano A, Andreozzi R, d’Ischia M. Water Res. 2004;38(2):414–422.10.1016/j.watres.2003.09.028Suche in Google Scholar PubMed

19. Ji YF, Zeng C, Zhou L, Yang X, Gao SX. Acta Sci Circumstantiae. 2012;32(6):1357–1363.Suche in Google Scholar

20. Philip J, Szulczewski DH. J Pharm Sci. 1973;62(9):1479–1482.10.1002/jps.2600620919Suche in Google Scholar PubMed

21. Encinas S, Bosca F, Miranda MA. Photochem Photobiol. 1998;68(5):640–645.Suche in Google Scholar

22. Venkatachalam K, Arzuaga X, Chopra N, Gavalas VG, Xu J, Bhattacharyya D,et al. J.Hazard.Mater. 2008;159:483–491.10.1016/j.jhazmat.2008.02.109Suche in Google Scholar PubMed PubMed Central

23. Quensen III JF, Tiedje JM, Boyd SA. Science (Washington). 1988;242(4879):752–754.10.1126/science.242.4879.752Suche in Google Scholar PubMed

24. Bedard DL, Quensen III JF. Microbial transformation and degradation of toxic organic chemicals, 1995:127–216. Wiley-Liss Inc., New York, NY.Suche in Google Scholar

Received: 2016-6-11
Revised: 2016-8-11
Accepted: 2016-8-22
Published Online: 2017-2-11
Published in Print: 2017-1-1

© 2017 by Walter De Gruyter GmbH

Artikel in diesem Heft

  1. Editorial: The importance of advanced oxidation processes in degrading persistent pollutants
  2. An overview on heterogeneous Fenton and photoFenton reactions using zerovalent iron materials
  3. Photooxidative Degradation of Pesticides in Water; Response Surface Modeling Approach
  4. The treatment of aniline in aqueous solutions by gamma irradiation
  5. Microwave regeneration of biological activated carbon
  6. Molecular iodine/aqueous NH4OAc: a green reaction system for direct oxidative synthesis of nitriles from amines
  7. Catalytic Degradation of Safranin T in Aqueous Medium Using Non-conventional Processes
  8. Oxidation of 1, 2-dichlorobenzene on a commercial V2O5-WO3/nano-TiO2 catalyst: Effect of HCl addition
  9. Current conduction mechanisms in thermal nitride and dry gate oxide grown on 4H-silicon carbide (SiC)
  10. Effect of light and oxygen on repetitive bacterial inactivation on uniform, adhesive, robust and stable Cu-polyester surfaces
  11. Wet oxidation of an industrial high concentration pharmaceutical wastewater using hydrogen peroxide as an oxidant
  12. Oxidation characteristics of heavy crude oil in ignition process
  13. Comparative studies on the performance of porous Ti/Sno2-Sb2O3/Pbo2 enhanced by CNT and Bi Co-doped electrodes for methyl orange oxidation
  14. Application of photocatalytic paint for destruction of benzo[a]pyrene. Impact of air humidity
  15. Spray-drying synthesis and characterization of Li4Ti5O12 anode material for lithium ion batteries
  16. Kinetics analysis of photocatalytic degradation of Acid Orange 7 by Co/N/Er3+: Y3Al5O12/TiO2 films
  17. Reaction characteristics of oxygen generation from plate-like potassium superoxide within a confined space
  18. Electrochemical reduction of CO2 on a Cu2O/polyaniline /stainless steel based electrode
  19. Role of oxygen-containing functional surface groups of activated carbons on the elimination of 2-hydroxybenzothiazole from waters in A hybrid heterogeneous ozonation system
  20. The degradation efficiency and mechanism of meclofenamic acid in aqueous solution by UV irradiation
  21. Effect of electrode oxide film in micro arc oxidation on water treatment
  22. Photocurrent response and photocatalytic activity of Nd-doped TiO2 thin films prepared by sol-gel method
  23. Mathematical model involving chemical reaction and mass transfer for the ozonation of dimethyl phthalate in water in a bubble column reactor
  24. Elimination of organic micro-contaminants in municipal wastewater by a combined immobilized biomass reactor and solar photo-Fenton tertiary treatment
  25. Degradation of catechol on BiOCl: charge transfer complex formation and photoactivity
  26. Photocatalytic degradation of phenol on strontium titanate supported on HZSM-5
  27. Selective Fenton-like catalytic oxidation of acid orange II on inorganic heterogeneous molecular imprinted catalysts
  28. Decoloration of azo dye methyl orange by a novel electro-Fenton internal circulation batch reactor
Heruntergeladen am 29.9.2025 von https://www.degruyterbrill.com/document/doi/10.1515/jaots-2016-0188/html
Button zum nach oben scrollen