Abstract
This study focuses on application of advanced oxidation (Photo-Fenton) processes to decolorize Basic Turquise Blue (BTB) X-GB 250% and Basic Blue (BB) X-GRRL 250% dyes. The percent decolorization was studied in terms of effect of variation in intensity of UV light at optimum conditions of all the parameters (pH = 3.0, H2O2 = 4.8 mM, FeSO4 = 1.6 mM, temperature = 50 °C, time = 80 min for BTB X-GB, and pH = 5.0, H2O2 = 5.6 mM, FeSO4 = 2.0 mM, temperature = 40 °C, time = 60 min for BB X-GRRL). Maximum decolorization was obtained at maximum intensity (15660 counts/min) of UV light as 96.17% for BTB X-GB and 88.48% for BB X-GRRL. First order, 2nd order and BMG kinetic models were used to analyze the data obtained for intensity of UV light. BMG model gives us the higher values of correlation coefficients for all data of both the dyes. The results have shown that Photo-Fenton oxidation process is the beneficial and effective for oxidation treatment of waste water effluents containing dyes as main pollutants.
References
1. A. N. Soon, B. Hameed, Desalination 269 (2011) 1.10.1016/j.desal.2010.11.002Search in Google Scholar
2. S. Ghezali, A. Mahdad-Benzerdjeb, M. Ameri, A. Z. Bouyakoub, Chem. Int. 4 (2018) 24.Search in Google Scholar
3. E. B. Hassen, A. M. Asmare, Chem. Int. 5 (2019) 87.Search in Google Scholar
4. N. E. Ibisi, C. A. Asoluka, Chem. Int. 4 (2018) 52.Search in Google Scholar
5. K. Sharma Arun, S. Acharya, Z. Phys. Chem. 233 (2019) 691.10.1515/zpch-2018-1181Search in Google Scholar
6. N.-U.-H. Khan, N. Bhatti Haq, M. Iqbal, A. Nazir, Z. Phys. Chem. 233 (2019) 361.10.1515/zpch-2018-1194Search in Google Scholar
7. J.-W. Lee, S.-P. Choi, R. Thiruvenkatachari, W.-G. Shim, H. Moon, Dyes Pigments 69 (2006) 196.10.1016/j.dyepig.2005.03.008Search in Google Scholar
8. A. O. Majolagbe, A. A. Adeyi, O. Osibanjo, A. O. Adams, O. O. Ojuri, Chem. Int. 3 (2017) 58.Search in Google Scholar
9. N. M. S. A. M. Awwad, M. M. Aqarbeh, F. M. Abdulaziz, Chem. Int. 6 (2020) 42.Search in Google Scholar
10. S. Jafarinejad, Chem. Int. 3 (2017) 268.Search in Google Scholar
11. S. Jafarinejad, Chem. Int. 3 (2017) 241.Search in Google Scholar
12. F. I. K. a. A. M. A. M. Alasadi, Chem. Int. 5 (2019) 258.Search in Google Scholar
13. A. Malik, A. Khan, M. Humayun, Z. Phys. Chem. 233 (2019) 375.10.1515/zpch-2018-1190Search in Google Scholar
14. E. Forgacs, T. Cserhati, G. Oros, Environ. Int. 30 (2004) 953.10.1016/j.envint.2004.02.001Search in Google Scholar PubMed
15. A. D. Bokare, R. C. Chikate, C. V. Rode, K. M. Paknikar, Appl. Catal. B Environ. 79 (2008) 270.10.1016/j.apcatb.2007.10.033Search in Google Scholar
16. H. S. Freeman, Supramolecular Dye Chemistry. Topics in Current Chemistry, 258 Edited by Frank Würthner. Springer: Berlin, Heidelberg, New York. 2005. xii+ 324 pp., ACS Publications, 2006.Search in Google Scholar
17. L. H. Abdel-Rahman, A. M. Abu-Dief, M. Abd-El Sayed, M. M. Zikry, Chem. Mater. Res. 8 (2016) 8.Search in Google Scholar
18. L. Abdel-Rahman, B. Al-Farhan, A. Abu-Dief, M. Zikry, Arch. Chem. Res. 1 (2016) 1.Search in Google Scholar
19. A. M. Abu-Dief, M. M. Zikry, Int. J. Nanomater. Chem. 4 (2018) 27.10.18576/ijnc/040301Search in Google Scholar
20. M. H. Zonoozi, M. R. Alavi Moghaddam, M. Arami, Environ. Eng. Manag. J. 7 (2008) 695.10.30638/eemj.2008.092Search in Google Scholar
21. M. Iqbal, J. Nisar, J. Environ. Chem. Eng. 3 (2015) 1912.10.1016/j.jece.2015.06.011Search in Google Scholar
22. M. Iqbal, I. A. Bhatti, J. Hazard. Mater. 299 (2015) 351.10.1016/j.jhazmat.2015.06.045Search in Google Scholar
23. A. Bozdogan, H. Goknil, Billimeri Dergisi Sayi 4 (1987) 83.Search in Google Scholar
24. J. Wu, M. A. Eiteman, S. E. Law, J. Environ. Eng. 124 (1998) 272.10.1061/(ASCE)0733-9372(1998)124:3(272)Search in Google Scholar
25. N. M. Mahmoodi, M. Arami, N. Y. Limaee, N. S. Tabrizi, Chem. Eng. J. 112 (2005) 191.10.1016/j.cej.2005.07.008Search in Google Scholar
26. M. Z. Ahamd, S. Ehtisham-ul-Haque, N. Nisar, K. Qureshi, A. Ghaffar, M. Abbas, J. Nisar, M. Iqbal, Water Sci. Technol. 76 (2017) 323.10.2166/wst.2017.152Search in Google Scholar
27. A. M. Abu-Dief, W. S. Mohamed, Mater. Res. Express 4 (2017) 035039.10.1088/2053-1591/aa6712Search in Google Scholar
28. W. S. Mohamed, A. M. Abu-Dief, J. Phys. Chem. Solids 116 (2018) 375.10.1016/j.jpcs.2018.02.008Search in Google Scholar
29. C. Pearce, J. Lloyd, J. Guthrie, Dyes Pigments 58 (2003) 179.10.1016/S0143-7208(03)00064-0Search in Google Scholar
30. A. Singh, S. Rani, N. R. Bishnoi, Ecol. Eng. 47 (2012) 291.10.1016/j.ecoleng.2012.07.001Search in Google Scholar
31. F. Akbal, J. Colloid Interface Sci. 286 (2005) 455.10.1016/j.jcis.2005.01.036Search in Google Scholar PubMed
32. M. Muruganandham, M. Swaminathan, Dyes Pigments 63 (2004) 315.10.1016/j.dyepig.2004.03.004Search in Google Scholar
33. M. S. Lucas, J. A. Peres, Dyes Pigments 71 (2006) 236.10.1016/j.dyepig.2005.07.007Search in Google Scholar
34. H. Park, W. Choi, J. Photochem. Photobiol. A Chem. 159 (2003) 241.10.1016/S1010-6030(03)00141-2Search in Google Scholar
35. M. Ahmad, G. Abbas, R. Haider, F. Jalal, A. Shar Ghulam, A. Soomro Gul, N. Qureshi, M. Iqbal, A. Nazir, Z. Phys. Chem. (2019). [Epub ahead of print].Search in Google Scholar
36. I. Bibi, S. Hussain, F. Majid, S. Kamal, S. Ata, M. Sultan, I. Din Muhammad, M. Iqbal, A. Nazir, Z. Phys. Chem. (2019). [Epub ahead of print].Search in Google Scholar
37. Y. Wang, J. Song, Z. Phys. Chem. (2019). [Epub ahead of print].Search in Google Scholar
38. S.-F. Kang, C.-H. Liao, S.-T. Po, Chemosphere 41 (2000) 1287.10.1016/S0045-6535(99)00524-XSearch in Google Scholar
39. G. Ruppert, R. Bauer, G. Heisler, J. Photochem. Photobiol. A Chem. 73 (1993) 75.10.1016/1010-6030(93)80035-8Search in Google Scholar
40. Y. Sun, J. J. Pignatello, Environ. Sci. Technol. 27 (1993) 304.10.1021/es00039a010Search in Google Scholar
41. A. Jamil, H. Bokhari Tanveer, M. Iqbal, A. Bhatti Ijaz, M. Zuber, J. Nisar, N. Masood, Z. Phys. Chem. (2019). [Epub ahead of print].Search in Google Scholar
42. S. Haji, B. Benstaali, N. Al-Bastaki, Chem. Eng. J. 168 (2011) 134.10.1016/j.cej.2010.12.050Search in Google Scholar
43. M. Behnajady, N. Modirshahla, F. Ghanbary, J. Hazard. Mater. 148 (2007) 98.10.1016/j.jhazmat.2007.02.003Search in Google Scholar PubMed
44. K. Legrouri, E. Khouya, H. Hannache, M. El Hartti, M. Ezzine, R. Naslain, Chem. Int. 3 (2017) 301.Search in Google Scholar
45. A. Abourriche, H. Hannache, M. Oumam, Chem. Int. 4 (2018) 7.Search in Google Scholar
46. N. Modirshahla, M. Behnajady, F. Ghanbary, Dyes Pigments 73 (2007) 305.10.1016/j.dyepig.2006.01.002Search in Google Scholar
47. J.-H. Sun, S.-P. Sun, G.-L. Wang, L.-P. Qiao, Dyes Pigments 74 (2007) 647.10.1016/j.dyepig.2006.04.006Search in Google Scholar
48. M. Arshad, A. Qayyum, G. A. Shar, G. A. Soomro, A. Nazir, B. Munir, M. Iqbal, J. Photochem. Photobiol. B Biol. 185 (2018) 176.10.1016/j.jphotobiol.2018.04.043Search in Google Scholar PubMed
49. M. Arshad, A. Qayyum, G. Abbas, R. Haider, M. Iqbal, A. Nazir, J. Mol. Liq. 260 (2018) 272.10.1016/j.molliq.2018.03.074Search in Google Scholar
50. M. Iqbal, J. Nisar, M. Adil, M. Abbas, M. Riaz, M. A. Tahir, M. Younus, M. Shahid, Chemosphere 168 (2017) 590.10.1016/j.chemosphere.2016.11.021Search in Google Scholar PubMed
51. J.-H. Sun, S.-H. Shi, Y.-F. Lee, S.-P. Sun, Chem. Eng. J. 155 (2009) 680.10.1016/j.cej.2009.08.027Search in Google Scholar
52. R. M. A. Aal, M. A. Gitru, Z. M. Essam, Chem. Int. 3 (2017) 358.Search in Google Scholar
53. T. N. Chikwe, R. E. Ekpo, I. Okoye, Chem. Int. 4 (2018) 230.Search in Google Scholar
54. K. Djehaf, A. Z. Bouyakoub, R. Ouhib, H. Benmansour, A. Bentouaf, A. Mahdad, N. Moulay, D. Bensaid, M. Ameri, Chem. Int. 3 (2017) 414.Search in Google Scholar
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