Degradation of refractory dibutyl phthalate by peroxymonosulfate activated with novel catalysts cobalt metal-organic frameworks: Mechanism, performance, and stability

Journal of Hazardous Materials

Volumn 318, Issue , 2016, Pages 154-163

  Li, Huanxuan ^a,b   Wan, Jinquan ^a   Ma, Yongwen ^a   Wang, Yan ^a   Chen, Xi ^b   Guan, Zeyu ^a  

^a SOUTH CHINA UNIVERSITY OF TECHNOLOGY   (China)

^b Department of Earth and Environmental Sciences   (United States)

Author keywords

Activation mechanism; Cobalt metal organic frameworks; Degradation; Dibutyl phthalate; Peroxymonosulfate

Indexed keywords

CATALYST ACTIVITY; CATALYSTS; CHEMICAL ACTIVATION; COBALT; CRYSTALLINE MATERIALS; DEGRADATION; ESTERS; ORGANIC POLYMERS; ORGANOMETALLICS; REFRACTORY MATERIALS; REFRACTORY METALS;

ACTIVATION MECHANISMS; DEGRADATION EFFICIENCY; DI-BUTYL PHTHALATE; HETEROGENEOUS CATALYST; HETEROGENEOUS REACTIONS; METAL ORGANIC FRAMEWORK; PEROXYMONOSULFATE; POSSIBLE MECHANISMS;

BIODEGRADATION;

COBALT; HYDROXYL RADICAL; METAL ORGANIC FRAMEWORK; PEROXYMONOSULFATE; PHTHALIC ACID DIBUTYL ESTER; SULFATE; UNCLASSIFIED DRUG;

CATALYST; COBALT; DEGRADATION; HYDROXYL RADICAL; PH; PHTHALATE; REDUCTION; SULFATE;

ANALYTIC METHOD; ARTICLE; CATALYST; CRYSTALLIZATION; DEGRADATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MORPHOLOGY; OXIDATION; PH; SCANNING ELECTRON MICROSCOPY; SYNTHESIS; X RAY DIFFRACTION; X RAY PHOTOELECTRON SPECTROSCOPY;

EID: 84978039477     PISSN: 03043894     EISSN: 18733336     Source Type: Journal    
DOI: 10.1016/j.jhazmat.2016.06.058     Document Type: Article

References (50)

1. [1] Neta, P., Huie, R.E., Ross, A.B., Rate constants for reactions of inorganic radicals in aqueous solution. J. Phys. Chem. Chem. 17 (1988), 1027–1284.
2. [2] Ribeiro, A.R., Nunes, O.C., Pereira, M.F.R., Silva, A.M.T., An overview on the advanced oxidation processes applied for the treatment of water pollutants defined in the recently launched Directive 2013/39/EU. Environ. Int. 75 (2015), 33–51.
3. [3] Li, H.X., Wan, J.Q., Ma, Y.W., Wang, Y., Reaction pathway and oxidation mechanisms of dibutyl phthalate by persulfate activated with zero-valent iron. Sci. Total Environ. 56 (2016), 889–897.
4. [4] Wang, D.G., Li, Y.F., Yang, M., Han, M., Decomposition of polycyclic aromatic hydrocarbons in atmospheric aqueous droplets through sulfate anion radicals: an experimental and theoretical study. Sci. Total Environ. 393 (2008), 64–71.
5. [5] Rastogi, A., Al-Abed, S.R., Dionysiou, D.D., Sulfate radical-based ferrous–peroxymonosulfate oxidative system for PCBs degradation in aqueous and sediment systems. Appl. Catal. B. 85 (2009), 171–179.
6. [6] Li, H.X., Wan, J.Q., Ma, Y.W., Wang, Y., Chen, Y.M., Influence of particle size of zero-valent iron and dissolved silica on the reactivity of activated persulfate for degradation of acid orange 7. Chem. Eng. J. 237 (2014), 487–496.
7. [7] Tekin, H., Bilkay, O., Ataberk, S.S., Balta, T.H., Ceribasi, I.H., Sanin, F.D., Dilek, F.B., Yetis, U., Use of Fenton oxidation to improve the biodegradability of a pharmaceutical wastewater. J. Hazard. Mater. 136 (2006), 258–265.
8. [8] Xie, P.C., Ma, J., Liu, W., Zou, J., Yue, S.Y., Impact of UV/persulfate pretreatment on the formation of disinfection byproducts during subsequent chlorination of natural organic matter. Chem. Eng. J. 269 (2015), 203–211.
9. [9] Li, H.X., Wan, J.Q., Ma, Y.W., Huang, M.Z., Wang, Y., Chen, Y.M., New insights into the role of zero-valent iron surface oxidation layers in persulfate oxidation of dibutyl phthalate solutions. Chem. Eng. J. 250 (2014), 137–147.
10. [10] Anipsitakis, G.P., Dionysiou, D.D., Degradation of organic contaminants in water with sulfate radicals generated by the conjunction of peroxymonosulfate with cobalt. Environ. Sci. Technol. 37 (2003), 4790–4797.
11. [11] Zhang, B.T., Xiang, W.X., Jiang, X.M., Zhang, Y., Teng, Y.G., Oxidation of dyes by alkaline-activated peroxymonosulfate. J. Environ. Eng. 04016003 (2016), 1–6.
12. [12] Anipsitakis, G.P., Dionysiou, D.D., Radical generation by the interaction of transition metals with common oxidants. Environ. Sci. Technol. 38 (2004), 3705–3709.
13. 4 magnetic nanoparticles as a highly active heterogeneous catalyst of oxone for the degradation of diclofenac in water. J. Hazard. Mater. 262 (2013), 836–844.
14. [14] Fernandez, J., Maruthamuthu, P., Kiwi, J., Photobleaching and mineralization of Orange II by oxone and metal-ions involving fention-like chemistry under visible light. J. Photochem. Photobiol. A 161 (2004), 185–192.
15. [15] Pagano, M., Volpe, A., Mascolo, G., Lopez, A., Locaputo, V., Ciannarella, R., Perxymonosulfate-Co(II) oxidation system for the removal of the nonionic surfactant Brji 35 from aqueous solution. Chemosphere 86 (2012), 329–334.
16. [16] Shukla, P., Sun, H.Q., Wang, S.B., Ang, H.M., Tadé, M.O., Co-SBA-15 for heterogeneous oxidation of phenol with sulfate radical for wastewater treatment. Catal. Today 175 (2011), 380–385.
17. 4/peroxymonosulfate system: kinetics and mechanism study using Acid Orange 7 as a model compound. Appl. Catal. B: Environ. 80 (2008), 116–121.
18. 4 nanocrystals on graphene oxide as a synergistic catalyst for degradation of Orange II in water by advanced oxidation technology based on sulfate radicals. Catal. Today 175 (2011), 380–385.
19. [19] Rowsell, J.L.C., Yagui, O.M., Metal-organic frameworks: a new class of porous materials. Microporous Mesoporous Mater. 73 (2004), 3–14.
20. [20] Kuppler, R.J., Timmons, D.J., Fang, Q.R., Li, J.R., Makal, T.A., Young, M.D., Yuan, D.Q., Zhao, D., Zhuang, W.J., Zhou, H.C., Potential applications of metal-organic frameworks. Coord. Chem. Rev. 253 (2009), 3042–3066.
21. [21] Andrew Lin, K.Y., Changa, H.A., Hsua, C.J., Iron-based metal organic framework MIL-88A, as a heterogeneous persulfate catalyst for decolorization of Rhodamine B in water. RSC Adv. 5 (2015), 32520–32530.
22. [22] Du, J.J., Yuan, Y.P., Sun, J.X., Peng, F.M., Jiang, X., Qiu, L.G., Xie, A.J., Shen, Y.H., Zhu, J.F., New photocatalysts based on MIL-53 metal-organic frameworks for the decolorization of methylene blue dye. J. Hazard. Mater. 190 (2011), 945–951.
23. [23] Wang, D.K., Wang, M.T., Li, Z.H., Fe-based metal-organic frameworks for highly selective photocatalytic benzene hydroxylation to phenol. ACS Catal. 5 (2015), 6852–6857.
24. [24] Yang, G.P., Zhao, X.K., Sun, X.J., Lu, X.L., Oxidative degradation of diethyl phthalate by photochemically-enhanced Fenton reaction. J. Hazard. Mater. B 126 (2005), 112–118.
25. [25] Jaworska, J.S., Hunter, R.S., Schultz, T.W., Quantitative structure-toxicity relationships and volume fraction analyses for selected esters. Arch. Environ. Contam. Toxicol. 29 (1995), 86–93.
26. [26] Lyche, J.L., Gutleb, A.C., Bergman, A., Eriksen, G.S., Murk, A.J., Ropstad, E., Saunders, M., Skaare, J.U., Reproductive and developmental toxicity of phthalates. J. Toxicol. Environ. Health Part B: Crit. Rev. 12 (2009), 225–249.
27. [27] Ejlertsson, J., Alnervik, M., Jonsson, S., Svensson, B.H., Influence of water solubility side-chain degradability, and side-chain structure on the degradation of phthalic acid esters under methanogenic conditions. Environ. Sci. Technol. 31 (1997), 2761–2764.
28. [28] Yaghi, O.M., Li, H., Groy, T.L., Construction of porous solids from hydrogenbonded metal complexes of 1,3,5-benzenetricarboxylic acid. J. Am. Chem. Soc. 118 (1996), 9096–9101.
29. [29] Yaghi, O.M., Li, H., Davis, C., Richardson, D., Groy, T.L., Synthetic strategies structure patterns, and emerging properties in the chemistry of modular porous solids. Acc. Chem. Res. 31 (1998), 474–484.
30. 2∙12H2O and its catalytic activity in CO oxidation reaction. J. Wuhan Univ. Technol. Mater. Sci. Ed., 2015, 71–75.
31. [31] Seo, Y.K., Yoon, J.W., Lee, J.S., Lee, U.H., Hwang, Y.K., Jun, C.H., Horcajada, P., Serre, C., Chang, J.S., Large scale fluorine-free synthesis of hierarchically porous iron (III) trimesate MIL-100(Fe) with a zeolite MTN topology. Microporous Mesoporous Mater. 157 (2012), 137–145.
32. [32] Lin, S., Song, Z.L., Che, G.B., Ren, A., Li, P., Liu, C.B., Zhang, J.H., Adsorption behavior of metal-organic frameworks for methylene blue from aqueous solution. Microporous Mesoporous Mater. 193 (2014), 27–34.
33. [33] Crane, J.L., Anderson, K.E., Conway, S.G., Hydrothermal synthesis and characterization of a metal-organic framework by thermogravimetric analysis, powder X-ray diffraction, and infrared spectroscopy: an integrative inorganic chemistry experiment. J. Chem. Educ. 92 (2015), 373–377.
34. [34] Lv, H.L., Zhao, H.Y., Cao, T.C., Qian, L., Wang, Y.B., Zhao, G.H., Efficient degradation of high concentration azo-dye wastewater by heterogeneous Fenton process with iron-based metal-organic framework. J. Mol. Catal. A Chem. 400 (2015), 81–89.
35. [35] Yun, R.R., Lu, Z.Y., Pan, Y., You, X.Z., Bai, J.F., Formation of a metal-organic framework with high surface area and gas uptake by Breaking edges off truncated cuboctahedral cages. Angew. Chem. Int. Ed. 52 (2013), 11282–11285.
36. 3 under ultrasound. Bull. Korean Chem. Soc. 30 (2009), 2921–2926.
37. 3. J. Am. Chem. Soc. 127 (2005), 9376–9377.
38. [38] Ma, S.Q., Wang, X.S., Collier, C.D., Manis, E.S., Zhou, H.C., Ultramicroporous metal-organic framework based on 9, 10-anthracenedicarboxylate for selective gas adsorption. Inorg. Chem. 46 (2007), 8499–8501.
39. 3 in heterogeneous activation of peroxymonosulfate for decolorization of Rhodamine B. Chem. Eng. J. 231 (2013), 434–440.
40. [40] Gong, F., Wang, L., Li, D., Zhou, F., Yao, Y., Lu, W., Huang, S., Chen, W., An effective heterogeneous iron-based catalyst to activate peroxymonosulfate for organic contaminants removal. Chem. Eng. J. 267 (2015), 102–110.
41. [41] Furman, O.S., Teel, A.L., Watts, R.J., Mechanism of base activation of Persulfate. Environ. Sci. Technol. 44 (2010), 6423–6428.
42. [42] Guan, Y.H., Ma, J., Li, X.C., Fang, J.Y., Chen, L.W., Influence of pH on the formation of sulfate and hydroxyl radicals in the UV/peroxymonosulfate system. Environ. Sci. Technol. 45 (2011), 9308–9314.
43. [43] Feng, Y., Liu, J.H., Wu, D.L., Zhou, Z.Y., Deng, Y., Zhang, T., Shi, K.M., Efficient degradation of sulfamethazine with CuCo2O4 spinel nanocatalysts for peroxymonosulfate activation. Chem. Eng. J. 280 (2015), 514–524.
44. 4 nanocatalysts for degradation of rhodamine B. J. Hazard. Mater. 244–245 (2013), 736–742.
45. 2+ −catalyst. J. Hazard. Mater. 170 (2009), 1110–1118.
46. 4 concave nanocubes with high specific surface area and their gas sensing properties. ACS Appl. Mater. Interfaces 6 (2014), 4186–4195.
47. 4/Raschig rings in the presence of oxone. J. Mol. Catal. A: Chem. 272 (2007), 11–19.
48. 4: kinetics and transformation intermediates. Environ. Sci. Technol., 2016, 10.1021/acs.est.6b00701.
49. [49] Song, Y.H., Wei, C.T., He, J., Li, X., Lu, X.P., Wang, L., Porous Co nanobeads/rGO nanocomposites derived from rGO/Co-metal organic frameworks for glucose sensing. Sens. Actuators B Chem. 220 (2015), 1056–1063.
50. [50] Yang, X., Tang, Y. Bing, Huang, X., Xue, H.T., Kang, W.P., Li, W.Y., Ng, T.W., Lee, C.S., Lithium ion battery application of porous composite oxide microcubes prepared via metal-organic frameworks. J. Power Sources 284 (2015), 109–114.