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Removal of Personal Care Products Through Ferrate(VI) Oxidation Treatment

  • Bin Yang
  • Guang-Guo YingEmail author
Chapter
Part of the The Handbook of Environmental Chemistry book series (HEC, volume 36)

Abstract

Personal care products (PCPs) have been widely used in daily life and continually introduced to the aquatic environment, posing potential risks to the aquatic ecosystem and human health. Due to incomplete removal of PCPs in traditional wastewater and water treatment systems, advanced oxidation technologies can be applied to increase the removal efficiency of those PCPs. As a powerful oxidant, ferrate(VI) (Fe(VI)) has a great potential for removal of PCPs during water treatment. In this chapter, we firstly introduced the aqueous chemistry of Fe(VI); then critically reviewed the reaction mechanisms of Fe(VI) with typical PCPs by using removal rates, reaction kinetics, linear free-energy relationships, products identification, and toxicity evaluation; and finally discussed the removal of PCPs during water treatment by Fe(VI). Published phenolic and nitrogen-containing PCPs can be completely removed by Fe(VI) oxidation treatment except triclocarban. The reactions between the PCPs and Fe(VI) follows second-order reaction kinetics with the apparent second-order rate constants (k app) ranging from 7 to 1,111 M−1 s−1 at pH 7.0. The reactivity of Fe(VI) species with the PCPs has the following decreasing order of H2FeO4 > HFeO4  > FeO4 2−, through the electrophilic oxidation mechanism. The phenolic PCPs can be transformed by Fe(VI) oxidation based on phenoxyl radical reaction, degradation, and coupling reaction. More importantly, the oxidation of each phenolic PCPs by Fe(VI) leads to the loss of its corresponding toxicity. The coexisting constituents present in source water have significant effects on PCP removal during Fe(VI) oxidation treatment. In practical applications, in situ production of Fe(VI) solution appears to be a promising technology for removal of PCPs during pilot and full-scale water treatment.

Keywords

Coexisting constituents Ferrate(VI) In situ Oxidation Personal care products Reaction mechanisms 

Abbreviations

5CBT

5-Chloro-1H-benzotriazole

5MBT

5-Methyl-1H-benzotriazole

ABTS

2,2′-Azinobis-(3-ethylbenzothiazoline-6-sulfonate)

AHTN

7-Acetyl-1,1,3,4,4,6-hexamethyl-tetralin

BP-3

Benzophenone-3

BT

1H-benzotriazole

BTs

Benzotriazoles

DMBT

5,6-Dimethyl-1H-benzotriazole hydrate

DOC

Dissolved organic carbon

Fe(III)

Ferric hydroxide

Fe(V)

Ferrate(V)

Fe(VI)

Ferrate(VI)

GC–MS

Gas chromatography–mass spectrometry

HA

Humic acid

HBT

1-Hydroxybenzotriazole

HHCB

1,3,4,6,7,8-Hexahydro-4,6,6,7,8,8-hexamethylcyclopenta-γ-2-benzopyrane

I

Iodide

kapp

Apparent second-order rate constants

PCPs

Personal care products

pKa

Acid dissociation constants

RRLC–MS/MS

Rapid resolution liquid chromatography–tandem mass spectrometry

t1/2

Half-life

TCC

Triclocarban

TCS

Triclosan

References

  1. 1.
    Chen Z-F, Ying G-G, Lai H-J, Chen F, Su H-C, Liu Y-S, Peng F-Q, Zhao J-L (2012) Determination of biocides in different environmental matrices by use of ultra-high-performance liquid chromatography-tandem mass spectrometry. Anal Bioanal Chem 404(10):3175–3188CrossRefGoogle Scholar
  2. 2.
    Bu Q, Wang B, Huang J, Deng S, Yu G (2013) Pharmaceuticals and personal care products in the aquatic environment in China: a review. J Hazard Mater 262:189–211CrossRefGoogle Scholar
  3. 3.
    Liu JL, Wong MH (2013) Pharmaceuticals and personal care products (PPCPs): a review on environmental contamination in China. Environ Int 59:208–224CrossRefGoogle Scholar
  4. 4.
    Brausch JM, Rand GM (2011) A review of personal care products in the aquatic environment: environmental concentrations and toxicity. Chemosphere 82(11):1518–1532CrossRefGoogle Scholar
  5. 5.
    Witorsch RJ, Thomas JA (2010) Personal care products and endocrine disruption: a critical review of the literature. Crit Rev Toxicol 40:1–30CrossRefGoogle Scholar
  6. 6.
    Jiang JQ, Lloyd B (2002) Progress in the development and use of ferrate(VI) salt as an oxidant and coagulant for water and wastewater treatment. Water Res 36(6):1397–1408CrossRefGoogle Scholar
  7. 7.
    Sharma VK (2002) Potassium ferrate(VI): an environmentally friendly oxidant. Adv Environ Res 6(2):143–156CrossRefGoogle Scholar
  8. 8.
    Lee Y, Cho M, Kim JY, Yoon J (2004) Chemistry of ferrate (Fe(VI)) in aqueous solution and its applications as a green chemical. J Ind Eng Chem 10(1):161–171Google Scholar
  9. 9.
    Lee Y, Zimmermann SG, Kieu AT, von Gunten U (2009) Ferrate (Fe(VI)) application for municipal wastewater treatment: a novel process for simultaneous micropollutant oxidation and phosphate removal. Environ Sci Technol 43(10):3831–3838CrossRefGoogle Scholar
  10. 10.
    Yang B, Ying G-G, Zhao J-L, Liu S, Zhou L-J, Chen F (2012) Removal of selected endocrine disrupting chemicals (EDCs) and pharmaceuticals and personal care products (PPCPs) during ferrate(VI) treatment of secondary wastewater effluents. Water Res 46(7):2194–2204CrossRefGoogle Scholar
  11. 11.
    Jiang JQ, Zhou ZW (2013) Removal of pharmaceutical residues by Ferrate(VI). PLoS One 8(2):e55729CrossRefGoogle Scholar
  12. 12.
    Sharma VK (2013) Ferrate(VI) and ferrate(V) oxidation of organic compounds: kinetics and mechanism. Coord Chem Rev 257(2):495–510CrossRefGoogle Scholar
  13. 13.
    Sharma VK (2011) Oxidation of inorganic contaminants by ferrates (VI, V, and IV)-kinetics and mechanisms: a review. J Environ Manag 92(4):1051–1073CrossRefGoogle Scholar
  14. 14.
    Prucek R, Tucek J, Kolarik J, Filip J, Marusak Z, Sharma VK, Zboril R (2013) Ferrate(VI)-induced arsenite and arsenate removal by in situ structural incorporation into magnetic iron(III) oxide nanoparticles. Environ Sci Technol 47(7):3283–3292Google Scholar
  15. 15.
    Cho M, Lee Y, Choi W, Chung HM, Yoon J (2006) Study on Fe(VI) species as a disinfectant: quantitative evaluation and modeling for inactivating Escherichia coli. Water Res 40(19):3580–3586CrossRefGoogle Scholar
  16. 16.
    Makky EA, Park GS, Choi IW, Cho SI, Kim H (2011) Comparison of Fe(VI) (FeO42-) and ozone in inactivating Bacillus subtilis spores. Chemosphere 83(9):1228–1233CrossRefGoogle Scholar
  17. 17.
    Gombos E, Felföldi T, Barkács K, Vértes C, Vajna B, Záray G (2012) Ferrate treatment for inactivation of bacterial community in municipal secondary effluent. Bioresour Technol 107:116–121CrossRefGoogle Scholar
  18. 18.
    Hu L, Page MA, Sigstam T, Kohn T, Mariñas BJ, Strathmann TJ (2012) Inactivation of bacteriophage MS2 with potassium Ferrate(VI). Environ Sci Technol 46(21):12079–12087CrossRefGoogle Scholar
  19. 19.
    Hu L, Martin HM, Arcs-Bulted O, Sugihara MN, Keatlng KA, Strathmann TJ (2009) Oxidation of carbamazepine by Mn(VII) and Fe(VI): Reaction kinetics and mechanism. Environ Sci Technol 43(2):509–515CrossRefGoogle Scholar
  20. 20.
    Sharma VK (2010) Oxidation of nitrogen-containing pollutants by novel ferrate(VI) technology: a review. J Environ Sci Health Part A Toxic 45(6):645–667CrossRefGoogle Scholar
  21. 21.
    Luo ZY, Strouse M, Jiang JQ, Sharma VK (2011) Methodologies for the analytical determination of ferrate(VI): a review. J Environ Sci Health Part A Toxic 46(5):453–460CrossRefGoogle Scholar
  22. 22.
    Lee Y, Yoon J, von Gunten U (2005) Spectrophotometric determination of ferrate (Fe(VI)) in water by ABTS. Water Res 39(10):1946–1953CrossRefGoogle Scholar
  23. 23.
    Lee Y, Yoon J, Von Gunten U (2005) Kinetics of the oxidation of phenols and phenolic endocrine disruptors during water treatment with ferrate (Fe(VI)). Environ Sci Technol 39(22):8978–8984CrossRefGoogle Scholar
  24. 24.
    Licht S, Yu XW (2005) Electrochemical alkaline Fe(VI) water purification and remediation. Environ Sci Technol 39(20):8071–8076CrossRefGoogle Scholar
  25. 25.
    Rule KL, Ebbett VR, Vikesland PJ (2005) Formation of chloroform and chlorinated organics by free-chlorine-mediated oxidation of triclosan. Environ Sci Technol 39(9):3176–3185CrossRefGoogle Scholar
  26. 26.
    Sharma VK, Burnett CR, Millero FJ (2001) Dissociation constants of the monoprotic ferrate(VI) ion in NaCl media. Phys Chem Chem Phys 3(11):2059–2062CrossRefGoogle Scholar
  27. 27.
    Goff H, Murmann RK (1971) Studies on mechanism of isotopic oxygen exchange and reduction of ferrate(VI) ion (FeO4 2-). J Am Chem Soc 93(23):6058–6065CrossRefGoogle Scholar
  28. 28.
    Schreyer JM, Ockerman LT (1951) Stability of the ferrate(VI) ion in aqueous solution. Anal Chem 23(9):1312–1314CrossRefGoogle Scholar
  29. 29.
    Yang B, Ying G-G, Zhao J-L, Zhang L-J, Fang Y-X, Nghiem LD (2011) Oxidation of triclosan by ferrate: reaction kinetics, products identification and toxicity evaluation. J Hazard Mater 186(1):227–235CrossRefGoogle Scholar
  30. 30.
    Yang B, Ying G-G, Zhang L-J, Zhou L-J, Liu S, Fang Y-X (2011) Kinetics modeling and reaction mechanism of ferrate(VI) oxidation of benzotriazoles. Water Res 45(6):2261–2269CrossRefGoogle Scholar
  31. 31.
    Yang B, Ying G-G (2013) Oxidation of benzophenone-3 during water treatment with ferrate(VI). Water Res 47(7):2458–2466CrossRefGoogle Scholar
  32. 32.
    Kamachi T, Kouno T, Yoshizawa K (2005) Participation of multioxidants in the pH dependence of the reactivity of ferrate(VI). J Org Chem 70(11):4380–4388CrossRefGoogle Scholar
  33. 33.
    Mvula E, von Sonntag C (2003) Ozonolysis of phenols in aqueous solution. Org Biomol Chem 1(10):1749–1756CrossRefGoogle Scholar
  34. 34.
    Suarez S, Dodd MC, Omil F, von Gunten U (2007) Kinetics of triclosan oxidation by aqueous ozone and consequent loss of antibacterial activity: relevance to municipal wastewater ozonation. Water Res 41(12):2481–2490CrossRefGoogle Scholar
  35. 35.
    Sharma VK, Mishra SK, Nesnas N (2006) Oxidation of sulfonamide antimicrobials by ferrate(VI) [(FeO4 2-)-O-VI]. Environ Sci Technol 40(23):7222–7227CrossRefGoogle Scholar
  36. 36.
    Li C, Li XZ, Graham N, Gao NY (2008) The aqueous degradation of bisphenol A and steroid estrogens by ferrate. Water Res 42(1–2):109–120CrossRefGoogle Scholar
  37. 37.
    Anquandah GAK, Sharma VK, Knight DA, Batchu SR, Gardinali PR (2011) Oxidation of trimethoprim by Ferrate(VI): kinetics, products, and antibacterial activity. Environ Sci Technol 45(24):10575–10581CrossRefGoogle Scholar
  38. 38.
    Zimmermann SG, Schmukat A, Schulz M, Benner J, Uv G, Ternes TA (2012) Kinetic and mechanistic investigations of the oxidation of tramadol by ferrate and ozone. Environ Sci Technol 46(2):876–884CrossRefGoogle Scholar
  39. 39.
    Casbeer EM, Sharma VK, Zajickova Z, Dionysiou DD (2013) Kinetics and mechanism of oxidation of tryptophan by Ferrate(VI). Environ Sci Technol 47(9):4572–4580CrossRefGoogle Scholar
  40. 40.
    Rush JD, Cyr JE, Zhao ZW, Bielski BHJ (1995) The oxidation of phenol by ferrate(VI) and ferrate(V) – a pulse-radiolysis and stopped-flow study. Free Radic Res 22(4):349–360CrossRefGoogle Scholar
  41. 41.
    Huang H, Sommerfeld D, Dunn BC, Eyring EM, Lloyd CR (2001) Ferrate(VI) oxidation of aqueous phenol: kinetics and mechanism. J Phys Chem A 105(14):3536–3541CrossRefGoogle Scholar
  42. 42.
    Lee Y, Escher BI, Von Gunten U (2008) Efficient removal of estrogenic activity during oxidative treatment of waters containing steroid estrogens. Environ Sci Technol 42(17):6333–6339CrossRefGoogle Scholar
  43. 43.
    Levy CW, Roujeinikova A, Sedelnikova S, Baker PJ, Stuitje AR, Slabas AR, Rice DW, Rafferty JB (1999) Molecular basis of triclosan activity. Nature 398(6726):383–384CrossRefGoogle Scholar
  44. 44.
    Schlumpf M, Cotton B, Conscience M, Haller V, Steinmann B, Lichtensteiger W (2001) In vitro and in vivo estrogenicity of UV screens. Environ Health Perspect 109(3):239–244CrossRefGoogle Scholar
  45. 45.
    Ma RS, Cotton B, Lichtensteiger W, Schlumpf M (2003) UV filters with antagonistic action at androgen receptors in the MDA-kb2 cell transcriptional-activation assay. Toxicol Sci 74(1):43–50CrossRefGoogle Scholar
  46. 46.
    Suzuki T, Kitamura S, Khota R, Sugihara K, Fujimoto N, Ohta S (2005) Estrogenic and antiandrogenic activities of 17 benzophenone derivatives used as UV stabilizers and sunscreens. Toxicol Appl Pharmacol 203(1):9–17CrossRefGoogle Scholar
  47. 47.
    Schultz TW, Seward JR, Sinks GD (2000) Estrogenicity of benzophenones evaluated with a recombinant yeast assay: comparison of experimental and rules-based predicted activity. Environ Toxicol Chem 19(2):301–304Google Scholar
  48. 48.
    Lee Y, von Gunten U (2010) Oxidative transformation of micropollutants during municipal wastewater treatment: Comparison of kinetic aspects of selective (chlorine, chlorine dioxide, ferrateVI, and ozone) and non-selective oxidants (hydroxyl radical). Water Res 44(2):555–566CrossRefGoogle Scholar
  49. 49.
    Sharma VK, Bloom JT, Joshi VN (1998) Oxidation of ammonia by ferrate(VI). J Environ Sci Health Part A Toxic 33(4):635–650CrossRefGoogle Scholar
  50. 50.
    Jiang J, Pang S-Y, Ma J, Liu H (2011) Oxidation of phenolic endocrine disrupting chemicals by potassium permanganate in synthetic and real waters. Environ Sci Technol 46(3):1774–1781CrossRefGoogle Scholar
  51. 51.
    Waite TD (2012) On-site production of ferrate for water and wastewater purification. Am Lab 44(10):26–28Google Scholar
  52. 52.
    Jiang JQ, Stanford C, Alsheyab M (2009) The online generation and application of ferrate(VI) for sewage treatment-A pilot scale trial. Sep Purif Technol 68(2):227–231CrossRefGoogle Scholar
  53. 53.
    Stanford C, Jiang JQ, Alsheyab M (2010) Electrochemical Production of Ferrate (Iron VI): application to the Wastewater Treatment on a Laboratory Scale and Comparison with Iron (III) Coagulant. Water Air Soil Pollut 209(1–4):483–488CrossRefGoogle Scholar
  54. 54.
    Jiang JQ, Stanford C, Alsheyab M (2012) The application of ferrate for sewage treatment: pilot- to full-scale trials. Global NEST J 14(1):93–99Google Scholar

Copyright information

© Springer International Publishing Switzerland 2014

Authors and Affiliations

  1. 1.State Key Laboratory of Organic Geochemistry, Guangzhou Institute of GeochemistryChinese Academy of SciencesGuangzhouChina

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