Efficient activation of peroxymonosulfate by magnetic Mn-MGO for degradation of bisphenol A

Journal of Hazardous Materials

Volumn 320, Issue , 2016, Pages 150-159

  Du, Jiangkun ^a   Bao, Jianguo ^a   Liu, Ying ^a   Ling, Haibo ^a   Zheng, Han ^a   Kim, Sang Hoon ^b   Dionysiou, Dionysios D ^c  

^a CHINA UNIVERSITY OF GEOSCIENCES   (China)

^b Korea Institute of Science and Technology   (South Korea)

^c 705 Engineering Research Center   (United States)

Author keywords

Bisphenol A; Degradation; Heterogeneous catalysis; Manganese oxide; Peroxymonosulfate activation

Indexed keywords

CATALYSIS; CATALYSTS; CHEMICAL ACTIVATION; DEGRADATION; ETHYLENE; ETHYLENE GLYCOL; FREE RADICAL REACTIONS; MAGNETIC RESONANCE; MANGANESE OXIDE; MANGANESE REMOVAL (WATER TREATMENT); ORE REDUCTION; PARAMAGNETIC RESONANCE; PHENOLS; SULFUR COMPOUNDS;

BIS-PHENOL A; DEGRADATION PATHWAYS; ELECTRON PARAMAGNETIC RESONANCES (EPR); LONG TERM STABILITY; PEROXYMONOSULFATE; PEROXYMONOSULFATE ACTIVATIONS; POSSIBLE MECHANISMS; SIMULTANEOUS REDUCTION;

MANGANESE;

4,4' ISOPROPYLIDENEDIPHENOL; ETHYLENE GLYCOL; GRAPHENE OXIDE; HYDROXYL RADICAL; MAGNETITE; MANGANESE OXIDE; SULFATE;

CATALYSIS; CATALYST; DEGRADATION; ETHYLENE; HETEROGENEOUS MEDIUM; HYDROXYL RADICAL; MANGANESE OXIDE; ORGANIC COMPOUND; PEROXY RADICAL; PH; PHENOL; REDUCTION;

ARTICLE; CATALYST; DEGRADATION; ELECTRON SPIN RESONANCE; GAS CHROMATOGRAPHY; MASS SPECTROMETRY; PH; ROENTGEN SPECTROSCOPY; TRANSMISSION ELECTRON MICROSCOPY; X RAY PHOTOELECTRON SPECTROSCOPY;

EID: 84982273133     PISSN: 03043894     EISSN: 18733336     Source Type: Journal    
DOI: 10.1016/j.jhazmat.2016.08.021     Document Type: Article

References (50)

1. [1] Bolong, N., Ismail, A.F., Salim, M.R., Matsuura, T., A review of the effects of emerging contaminants in wastewater and options for their removal. Desalination 239 (2009), 229–246.
2. [2] Benotti, M.J., Trenholm, R.A., Vanderford, B.J., Holady, J.C., Stanford, B.D., Snyder, S.A., Pharmaceuticals and endocrine disrupting compounds in U.S. drinking water. Environ. Sci. Technol. 43 (2009), 597–603.
3. [3] Tohyama, S., Miyagawa, S., Lange, A., Ogino, Y., Mizutani, T., Tatarazako, N., Katsu, Y., Ihara, M., Tanaka, H., Ishibashi, H., Kobayashi, T., Tyler, C.R., Iguchi, T., Understanding the molecular basis for differences in responses of fish estrogen receptor subtypes to environmental estrogens. Environ. Sci. Technol. 49 (2015), 7439–7447.
4. [4] Yuan, S., Gou, N., Alshawabkeh, A.N., Gu, A.Z., Efficient degradation of contaminants of emerging concerns by a new electro-Fenton process with Ti/MMO cathode. Chemosphere 93 (2013), 2796–2804.
5. [5] Komesli, O.T., Muz, M., Ak, M.S., Bakırdere, S., Gokcay, C.F., Occurrence, fate and removal of endocrine disrupting compounds (EDCs) in Turkish wastewater treatment plants. Chem. Eng. J. 277 (2015), 202–208.
6. [6] Liu, Z., Kanjo, Y., Mizutani, S., Removal mechanisms for endocrine disrupting compounds (EDCs) in wastewater treatment—physical means, biodegradation, and chemical advanced oxidation: a review. Sci. Total Environ. 407 (2009), 731–748.
7. [7] Jiang, L.-h., Liu, Y.-g., Zeng, G.-m., Xiao, F.-y., Hu, X.-j., Hu, X., Wang, H., Li, T.-t., Zhou, L., Tan, X.-f., Removal of 17β-estradiol by few-layered graphene oxide nanosheets from aqueous solutions: external influence and adsorption mechanism. Chem. Eng. J. 284 (2016), 93–102.
8. [8] Rosenfeldt, E.J., Linden, K.G., Degradation of endocrine disrupting chemicals bisphenol A, ethinyl estradiol, and estradiol during UV photolysis and advanced oxidation processes. Environ. Sci. Technol. 38 (2004), 5476–5483.
9. [9] Esplugas, S., Bila, D.M., Krause, L.G.T., Dezotti, M., Ozonation and advanced oxidation technologies to remove endocrine disrupting chemicals (EDCs) and pharmaceuticals and personal care products (PPCPs) in water effluents. J. Hazard. Mater. 149 (2007), 631–642.
10. 2: a shift in pathway from hydrodechlorination to oxidation in the presence of ferrous ions. Environ. Sci. Technol. 46 (2012), 3398–3405.
11. 2 in advanced oxidation processes. J. Hazard. Mater. 275 (2014), 121–135.
12. [12] Rahim Pouran, S., Abdul Raman, A.A., Wan Daud, W.M.A., Review on the application of modified iron oxides as heterogeneous catalysts in Fenton reactions. J. Cleaner Prod. 64 (2014), 24–35.
13. [13] Yuan, S., Liao, P., Alshawabkeh, A.N., Electrolytic manipulation of persulfate reactivity by iron electrodes for trichloroethylene degradation in groundwater. Environ. Sci. Technol. 48 (2014), 656–663.
14. [14] Liang, C., Wang, Z.S., Bruell, C.J., Influence of pH on persulfate oxidation of TCE at ambient temperatures. Chemosphere 66 (2007), 106–113.
15. [15] Liang, C., Su, H.-W., Identification of sulfate and hydroxyl radicals in thermally activated persulfate. Ind. Eng. Chem. Res. 48 (2009), 5558–5562.
16. [16] Furman, O.S., Teel, A.L., Watts, R.J., Mechanism of base activation of persulfate. Environ. Sci. Technol. 44 (2010), 6423–6428.
17. −. Chem. Eng. J. 252 (2014), 393–403.
18. [18] He, X., de la Cruz, A.A., O'Shea, K.E., Dionysiou, D.D., Kinetics and mechanisms of cylindrospermopsin destruction by sulfate radical-based advanced oxidation processes. Water Res. 63 (2014), 168–178.
19. − transfer mechanisms. Appl. Catal. B: Environ. 96 (2010), 290–298.
20. [20] Anipsitakis, G.P., Dionysiou, D.D., Radical generation by the interaction of transition metals with common oxidants. Environ. Sci. Technol. 38 (2004), 3705–3712.
21. 4 as an activator of peroxymonosulfate for the degradation of a plasticizer. Chem. Eng. J. 263 (2015), 435–443.
22. 4 spinel in water: efficiency, stability, and mechanism. Environ. Sci. Technol. 47 (2013), 2784–2791.
23. [23] Yang, Q., Choi, H., Al-Abed, S.R., Dionysiou, D.D., Iron–cobalt mixed oxide nanocatalysts: heterogeneous peroxymonosulfate activation, cobalt leaching, and ferromagnetic properties for environmental applications. Appl. Catal. B: Environ. 88 (2009), 462–469.
24. [24] Hu, P., Long, M., Cobalt-catalyzed sulfate radical-based advanced oxidation: a review on heterogeneous catalysts and applications. Appl. Catal. B: Environ. 181 (2016), 103–117.
25. 4: mechanism, stability, and effects of pH and bicarbonate ions. Environ. Sci. Technol. 49 (2015), 6838–6845.
26. 4-graphene hybrid as heterogeneous catalysts of peroxymonosulfate activation for efficient degradation of aqueous organic pollutants. J. Hazard. Mater. 270 (2014), 61–70.
27. 4) for Fenton-like reaction in water. J. Hazard. Mater. 296 (2015), 128–137.
28. [28] Li, W., Wu, P.-x., Zhu, Y., Huang, Z.-j., Lu, Y.-h., Li, Y.-w., Dang, Z., Zhu, N.-w., Catalytic degradation of bisphenol A by CoMnAl mixed metal oxides catalyzed peroxymonosulfate: performance and mechanism. Chem. Eng. J. 279 (2015), 93–102.
29. 2 nanomaterials and their superior performance in catalytic phenol degradation. Environ. Sci. Technol. 47 (2013), 5882–5887.
30. 3 for catalytic phenol degradation in aqueous solution. Appl. Catal. B: Environ. 154–155 (2014), 246–251.
31. 4–reduced graphene oxide hybrids for catalytic decomposition of aqueous organics. Ind. Eng. Chem. Res. 52 (2013), 3637–3645.
32. [32] Luo, S., Duan, L., Sun, B., Wei, M., Li, X., Xu, A., Manganese oxide octahedral molecular sieve (OMS-2) as an effective catalyst for degradation of organic dyes in aqueous solutions in the presence of peroxymonosulfate. Appl. Catal. B: Environ. 164 (2015), 92–99.
33. 4/GO catalysts for degradation of Orange II in water by advanced oxidation technology based on sulfate radicals. Chem. Eng. J. 240 (2014), 264–270.
34. 4/carbon sphere/cobalt composites for catalytic oxidation of phenol solutions with sulfate radicals. Chem. Eng. J. 245 (2014), 1–9.
35. 4 nanorods on graphene sheets for supercapacitor electrodes with long cycle stability. Chem. Mater. 24 (2012), 1158–1164.
36. 4 with crystalline walls. Adv. Mater. 19 (2007), 4063–4066.
37. [37] Yamashita, T., Hayes, P., Analysis of XPS spectra of Fe2+ and Fe3+ ions in oxide materials. Appl. Surf. Sci. 254 (2008), 2441–2449.
38. 4 hybrid functional material for the electrocatalytic reduction of oxygen. ACS Appl. Mater. Interfaces 6 (2014), 2692–2699.
39. [39] Yao, Y., Mao, Y., Zheng, B., Huang, Z., Lu, W., Chen, W., Anchored iron ligands as an efficient Fenton-like catalyst for removal of dye pollutants at neutral pH. Ind. Eng. Chem. Res. 53 (2014), 8376–8384.
40. [40] Nfodzo, P., Choi, H., Triclosan decomposition by sulfate radicals: effects of oxidant and metal doses. Chem. Eng. J. 174 (2011), 629–634.
41. 4/peroxymonosulfate system: kinetics and mechanism study using Acid Orange 7 as a model compound. Appl. Catal. B: Environ. 80 (2008), 116–121.
42. 2 nanocatalyst for heterogeneous activation of peroxymonosulfate. RSC Adv. 3 (2013), 520–525.
43. [43] Duan, X., Su, C., Zhou, L., Sun, H., Suvorova, A., Odedairo, T., Zhu, Z., Shao, Z., Wang, S., Surface controlled generation of reactive radicals from persulfate by carbocatalysis on nanodiamonds. Appl. Catal. B: Environ. 194 (2016), 7–15.
44. 4 magnetic nanoparticles as heterogeneous activator of peroxymonosulfate. J. Hazard. Mater. 276 (2014), 452–460.
45. 4 nanocages derived from nanoscale metal–organic frameworks for removal of bisphenol A by activation of peroxymonosulfate. Appl. Catal. B: Environ. 181 (2016), 788–799.
46. [46] Poerschmann, J., Trommler, U., Górecki, T., Aromatic intermediate formation during oxidative degradation of Bisphenol A by homogeneous sub-stoichiometric Fenton reaction. Chemosphere 79 (2010), 975–986.
47. [47] Sharma, J., Mishra, I.M., Dionysiou, D.D., Kumar, V., Oxidative removal of bisphenol A by UV-C/peroxymonosulfate (PMS): kinetics, influence of co-existing chemicals and degradation pathway. Chem. Eng. J. 276 (2015), 193–204.
48. 2 photoassisted process for bisphenol a mineralization. Water Res. 44 (2010), 2245–2252.
49. [49] Lin, K., Liu, W., Gan, J., Oxidative removal of bisphenol A by Manganese dioxide: efficacy, products, and pathways. Environ. Sci. Technol. 43 (2009), 3860–3864.
50. 2 activation of peroxymonosulfate for catalytic phenol degradation in aqueous solutions. Catal. Commun. 26 (2012), 144–148.