A biotic Fe0-H2O system for nitrobenzene removal from groundwater

Chemical Engineering Journal

Volumn 226, Issue , 2013, Pages 14-21

  Wu, Jinhua ^a,b   Yin, Weizhao ^a,b   Gu, Jingjing ^a,b   Li, Ping ^a,b   Wang, Xiangde ^a,b   Yang, Bo ^c  

^a BEIJING UNIVERSITY OF POSTS AND TELECOMMUNICATIONS   (China)

^b SOUTH CHINA UNIVERSITY OF TECHNOLOGY   (China)

^c SHENZHEN UNIVERSITY   (China)

Author keywords

Microorganism; Nitrobenzene; Reduction; Zero valent iron

Indexed keywords

ANOXIC CONDITIONS; BATCH EXPERIMENTS; ELECTRON DONORS; LOW CONCENTRATIONS; ORGANIC SUBSTRATE; REDUCTION CAPACITY; SULFATE REDUCING; ZERO-VALENT IRON;

CHEMICALS REMOVAL (WATER TREATMENT); DISSOLVED OXYGEN; ETHANOL; EXPERIMENTS; GLUCOSE; GROUNDWATER; GROUNDWATER POLLUTION; IRON; MICROORGANISMS; NITRATES; NITROBENZENE; REDUCTION; SULFUR COMPOUNDS;

NITROGEN REMOVAL;

EID: 84877342772     PISSN: 13858947     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cej.2013.04.021     Document Type: Article

References (47)

1. Kuscu O.S., Sponza D.T. Effects of nitrobenzene concentration and hydraulic retention time on the treatment of nitrobenzene in sequential anaerobic baffled reactor(ABR)/continuously stirred tank reactor (CSTR) system. Bioresour. Technol. 2009, 100:2162-2170.
2. Haigler B.E., Spain J.C. Biotransformation of nitrobenzene by bacteria containing toluene degradative pathways. Appl. Environ. Microbiol. 1991, 57:3156-3162.
3. Kuscu O.S., Sponza D.T. Effect of increasing nitrobenzene loading rates on the performance of anaerobic migrating blanket reactor and sequential anaerobic migrating blanket reactor/completely stirred tank reactor system. J. Hazard. Mater. 2009, 168:390-399.
4. Anotai J., Sakulkittimasak P., Boonrattanakij N., Lu M.C. Kinetics of nitrobenzene oxidation and iron crystallization in fluidized-bed Fenton process. J. Hazard. Mater. 2009, 165:874-880.
5. Carlos L., Fabbri D., Capparelli A.L., Prevot A.B., Pramauro E., Einschlag F.S.G. Intermediate distributions and primary yields of phenolic products in nitrobenzene degradation by Fenton's reagent. Chemosphere 2008, 72:952-958.
6. Zhao L., Ma J., Sun Z.Z. Oxidation products and pathway of ceramic honeycomb-catalyzed ozonation for the degradation of nitrobenzene in aqueous solution. Appl. Catal. B 2008, 79:244-253.
7. Henderson A.D., Demond A.H. Long-term performance of zero-valentiron permeable reactive barriers: a critical review. Environ. Eng. Sci. 2007, 24:401-423.
8. Andrew B.C., Laurence H., Raymond L.D. Use of iron-based technologies in contaminated land and groundwater remediation: a review. Sci. Total Environ. 2008, 400:42-51.
9. Westerhoff P. Reduction of nitrate, bromate, and chlorate by ZVI. J. Environ. Eng. 2003, 129:10-16.
10. Gillham R.W., Ohannesin S.F. Enhanced degradation of halogenated aliphatics by zero-valent iron. Ground Water 1994, 32:958-967.
11. Agrawal A., Tratnyek P.G. Reduction of nitro aromatic compounds by zero-valent iron metal. Environ. Sci. Technol. 1996, 30:153-160.
12. White A.F., Paterson M.L. Reduction of aqueous transition metal species on the surface of Fe (II)-containing oxides. Geochim. Cosmochim. Acta 1996, 60:3799-3814.
13. 2O systems. J. Hazard. Mater. 2009, 168:1626-1631.
14. Noubactep C. The fundamental mechanism of aqueous contaminant removal by metallic iron. Water SA 2010, 36:663-670.
15. Scherer M.M., Richter S., Valentine R.L., Alvarez P.J.J. Chemistry and microbiology of permeable reactive barriers for in situ groundwater clean up: critical review. Environ. Sci. Technol. 2000, 30:363-411.
16. Noothen T.V., Springael D., Bastiaens L. Positive impact of microorganisms on the performance of laboratory-scale permeable reactive iron barriers. Environ. Sci. Technol. 2008, 42:1680-1686.
17. Weathers L.J., Parkin G.F., Alvarez P.J.J. Utilization of cathodic hydrogen as electron donor for chloroform cometabolism by a mixed methanogenic culture. Environ. Sci. Technol. 1997, 31:880-885.
18. Field J.A., Alvarez R.S. Biodegradability of chlorinated solvents and related chlorinated aliphatic compounds. Rev. Environ. Sci. Biotechnol. 2004, 3:185-254.
19. Oh B.T., Just C.L., Alvarez P.J.J. Hexahydro-1,3,5-trinitro-1,3,5-triazine mineralization by zerovalent iron and mixed anaerobic cultures. Environ. Sci. Technol. 2001, 35:4341-4346.
20. Gerlach R., Cunningham A.B., Caccavo F. Dissimilatory iron-reducing bacteria can influence the reduction of carbon tetrachloride by iron metal. Environ. Sci. Technol. 2004, 34:2461-2464.
21. Huang Y.H., Zhang T.C. Reduction of nitrobenzene and formation of corrosion coatings in zerovalent iron systems. Water Res. 2006, 40:3075-3082.
22. Nooten T.V., Lieben F., Dries J., Pirard E., Springael D., Bastiaens L. Impact of microbial activities on the mineralogy and performance of column-scale permeable reactive iron barriers operated under two different redox conditions. Environ. Sci. Technol. 2007, 41:5724-5730.
23. Karri S., Alvarez R.S., Field J.A. Zero valent iron as an electron-donor for methanogenesis and sulfate reduction in anaerobic sludge. Biotechol. Bioeng. 2005, 92:810-819.
24. Till B.A., Weathers L.J., Alvarez P.J.J. Fe(0)-supported autotrophic denitrification. Environ. Sci. Technol. 1998, 32:634-639.
25. Shin K.H., Cha D.K. Microbial reduction of nitrate in the presence of nanoscale zero-valent iron. Chemosphere 2008, 72:257-262.
26. Yu X.Y., Amrhein C., Deshusses M.A., Matsumoto M.R. Perchlorate reduction by autotrophic bacteria in the presence of zero-valent iron. Environ. Sci. Technol. 2006, 40:1328-1334.
27. Son A., Lee J., Chiu P.C., Kim B.J., Cha D.K. Microbial reduction of perchlorate with zero-valent iron. Water Res. 2006, 40:2027-2032.
28. Novak P.J., Daniels L., Parkin G.F. Enhanced dechlorination of carbon tetrachloride and chloroform in the presence of elemental iron and methanosarcina barkeri, methanosarcina thermophila, or methanosaeta concillii. Environ. Sci. Technol. 1998, 32:1438-1443.
29. Ma C.W., Wu Y.Q. Dechlorination of perchloroethylene using zero-valent metal and microbial community. Environ. Geol. 2008, 55:47-54.
30. Xiu Z.M., Jin Z.H., Li T.L., Mahendra S., Lowry G.V., Alvarez P.J.J. Effects of nano-scale zero-valent iron particles on a mixed culture dechlorinating trichloroethylene. Bioresour. Technol. 2010, 110:1141-1146.
31. 0 enhanced by a mixed culture containing two Dehalococcoides strains. Chemosphere 2004, 55:661-669.
32. Wang S.M., Tseng S.K. Reductive dechlorination of trichloroethylene by combining autotrophic hydrogen-bacteria and zero-valent iron particles. Bioresour. Technol. 2009, 100:111-117.
33. 2 using a microbial consortium. Biotechnol. Lett. 2004, 26:307-310.
34. Işşk M., Sponza D.T. Effects of alkalinity and co-substrate on the performance of an upflow anaerobic sludge blanket (UASB) reactor through decolorization of Congo Red azo dye. Bioresour. Technol. 2005, 96:633-643.
35. Yin W.Z., Wu J.H., Li P., Zhu N.W., Wu P.X., Yang B. Experimental study of zero-valent iron induced nitrobenzene reduction in groundwater: the effects of pH, iron dosage, oxygen and common dissolved anions. Chem. Eng. J. 2012, 184:198-204.
36. Kohn T., Livi J.T., Roberts A.L., Vilesland P.J. Longevity of granular iron in groundwater treatment processes: corrosion product development. Environ. Sci. Technol. 2005, 39:2867-2879.
37. Lo M.C., Lam S.C., Lai C.K. Hardness and carbonate effects on the reactivity of zero-valent iron for Cr(VI) removal. Water Res. 2006, 40:595-605.
38. Noubactep C. Metallic iron for water treatment: a knowledge system challenges mainstream science. Fresenius Environ. Bull. 2011, 20:2632-2637.
39. Yin W.Z., Wu J.H., Li P., Lin G.H., Wang X.D., Zhu B., Yang B. Reductive transformation of pentachloronitrobenzene by zero-valent iron and mixed anaerobic culture. Chem. Eng. J. 2012, 210:309-315.
40. 2+. Water Res. 2005, 39:1751-1760.
41. Schnell S., Bak F., Pefenning N. Anaerobic degradation of aniline and dihydroxybenzenes by newly isolated sulfate-reducing bacteria and description of Desuifobacterium anilini. Arch. Microbiol. 1989, 152:556-563.
42. Tezel U., Pavlostathis S.G. Transformation of benzalkonium chloride under nitrate reducing conditions. Environ. Sci. Technol. 2009, 43:1342-1348.
43. Kahng H.Y., Kukor J.J., Oh K.H. Characterization of strain HY99, a novel microorganism capable of aerobic and anaerobic degradation of aniline. FEMS Microbiol. Lett. 2000, 190:215-221.
44. Le C., Wu J.H., Deng S.B., Li P., Wang X.D., Zhu N.W., Wu P.X. Effects of common dissolved anions on the reduction of para-chloronitrobenzene by zero-valent iron in groundwater. Water Sci. Technol. 2011, 63:1485-1490.
45. De M.A., O'Connor O.A., Kosson D.S. Metabolism of aniline under different anaerobic electron-accepting andn nutritional conditions. Environ. Toxicol. Chem. 1994, 13:233-239.
46. Wu Y.G., Hui L., Li X., Zhang Y.Z., Zhang W.C. Degradation of aniline in weihe riverbed sediments under denitrification conditions. J. Environ. Sci. Health. A 2007, 42:413-419.
47. Pereira R., Pereira L., van der Zee F.P., Alves M.M. Fate of aniline and sulfanilic acid in UASB bioreactors under denitrifying conditions. Water Res. 2011, 45:191-200.