Mostrar el registro sencillo del ítem

Catalizadores homogéneos y heterogéneos de Fe3+, Co2+ y Cu2+ para la degradación de metilparatión en medio acuoso diluido

dc.creatorVela-Monroy, Cindy A.
dc.creatorSaavedra-Alemán, Martha J.
dc.creatorCarriazo-Baños, José G.
dc.date2016-07-30
dc.date.accessioned2021-03-18T21:02:46Z
dc.date.available2021-03-18T21:02:46Z
dc.identifierhttps://revistas.itm.edu.co/index.php/tecnologicas/article/view/43
dc.identifier10.22430/22565337.43
dc.identifier.urihttp://test.repositoriodigital.com:8080/handle/123456789/11380
dc.descriptionDegradation of pesticides (plaguicides, herbicides, fungicides, among others) in aqueous media is a subject of great importance for ensuring the water quality into numerous hydric sources. This work reports the assessment of homogeneous (metal ion solutions) and heterogeneous (oxides supported on alumina) systems that are based on Fe3+, Co2+ y Cu2+, which were used as catalysts for oxidation (degradation) of methyl parathion (a plaguicide) in aqueous solution. Hydrogen peroxide was herein used as oxidizing molecule under mild condition of reaction (25 ºC and atmospheric pressure). The solids were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Fe3+/H2O2 (Fenton system) was the most active homogeneous catalyst compared to Co2+/H2O2 and Cu2+/H2O2 systems. Solids catalysts such as cobalt, copper or iron oxides as well as mixed oxides supported on alumina were active at pH close to neutrality. Fe-Co-Cu/Al2O3, Co-Cu/Al2O3 and Fe-Co/Al2O3 mixed systems were solids with the highest catalytic activity. In addition, an important effect of the support (-Al2O3) on the reaction pH was observed, allowing to reach values close to that of the neutrality, and thus increasing the catalytic activity of both cobalt oxide and copper oxide species. These results allow advancing on a new pathway for searching catalysts to remove organophosphorous pesticides from residual waters.en-US
dc.descriptionLa degradación de pesticidas (plaguicidas, herbicidas, fungicidas, entre otros) en medio acuoso constituye un tema de enorme importancia que contribuye a asegurar la calidad del agua de numerosas fuentes hídricas. En el presente trabajo se realizó la evaluación de sistemas catalíticos homogéneos (iones metálicos en solución) y heterogéneos (óxidos soportados en alúmina), basados en Fe3+, Co2+ y Cu2+, en la oxidación (degradación) del plaguicida metilparatión en medio acuoso, empleando peróxido de hidrógeno como oxidante bajo condiciones suaves de reacción (25 ºC y presión atmosférica). Los sólidos se caracterizaron por difracción de rayos X y microscopía electrónica de barrido (SEM). El sistema Fe3+/H2O2 (sistema Fenton) constituye el catalizador homogéneo más activo, en comparación con los sistemas Co2+/H2O2 y Cu2+/H2O2. Los sólidos conformados por óxidos de cobalto, cobre o hierro y óxidos mixtos soportados en alúmina mostraron actividad catalítica a pH muy cercano a la neutralidad. Los sistemas mixtos Fe-Co-Cu/Al2O3, Co-Cu/Al2O3 y Fe-Co/Al2O3 fueron los sólidos de máxima actividad catalítica. Adicionalmente, se observó la influencia del soporte (-Al2O3) en el pH del medio de reacción, permitiendo el acercamiento de dichos valores a la neutralidad y con ello favoreciendo la actividad catalítica de los óxidos de cobalto y de cobre. Los resultados del presente estudio permiten avanzar en una nueva ruta de búsqueda de catalizadores para la eliminación de pesticidas organofosforados contaminantes de aguas residuales.es-ES
dc.formatapplication/pdf
dc.languagespa
dc.publisherInstituto Tecnológico Metropolitano (ITM)en-US
dc.relationhttps://revistas.itm.edu.co/index.php/tecnologicas/article/view/43/36
dc.relation/*ref*/M. Abdennouri, M. Baâlala, A. Galadi, M. El Makhfouk, M. Bensitel, K. Nohair, M. Sadiq, A. Boussaoud, and N. Barka, “Photocatalytic degradation of pesticides by titanium dioxide and titanium pillared purified clays,” Arab. J. Chem., vol. 9, pp. S313–S318, Sep. 2016. [2] K. Ikehata and M. G. M. El-din, “Aqueous pesticide degradation by hydrogen peroxide/ultraviolet irradiation and Fenton-type advanced oxidation processes: a review,” J. Environ. Eng. Sci., vol. 5, no. 2, pp. 81–135, 2006. [3] M. I. Badawy, M. Y. Ghaly, and T. A. Gad-Allah, “Advanced oxidation processes for the removal of organophosphorus pesticides from wastewater,” Desalination, vol. 194, no. 1–3, pp. 166–175, 2006. [4] E. Evgenidou, I. Konstantinou, K. Fytianos, and I. Poulios, “Oxidation of two organophosphorous insecticides by the photo-assisted Fenton reaction,” Water Res., vol. 41, no. 9, pp. 2015–2027, 2007. [5] S. Chiron, A. Fernandez-Alba, A. Rodriguez, and E. Garcia-Calvo, “Pesticide chemical oxidation: State-of-the-art,” Water Res., vol. 34, no. 2, pp. 366–377, 2000. [6] M. Segal-Rosenheimer and Y. Dubowski, “Photolysis of methyl-parathion thin films: Products, kinetics and quantum yields under different atmospheric conditions,” J. Photochem. Photobiol. A Chem., vol. 209, no. 2–3, pp. 193–202, 2010. [7] E. C. Wanamaker, G. C. Chingas, and O. M. McDougal, “Parathion hydrolysis revisited: In situ aqueous kinetics by 1H NMR,” Environ. Sci. Technol., vol. 47, no. 16, pp. 9267–9273, 2013. [8] R. Thota and V. Ganesh, “Selective and sensitive electrochemical detection of methyl parathion using chemically modified overhead projector sheets as flexible electrodes,” Sensors Actuators, B Chem., vol. 227, pp. 169–177, 2016. [9] M. Diagne, N. Oturan, and M. A. Oturan, “Removal of methyl parathion from water by electrochemically generated Fenton’s reagent,” Chemosphere, vol. 66, no. 5, pp. 841–848, 2007. [10] C. Chávez-López, A. Blanco-Jarvio, M. Luna-Guido, L. Dendooven, and N. Cabirol, “Removal of methyl parathion from a chinampa agricultural soil of Xochimilco Mexico: A laboratory study,” Eur. J. Soil Biol., vol. 47, no. 4, pp. 264–269, 2011. [11] J. M. Pisani, W. E. Grant, and M. A. Mora, “Simulating the impact of cholinesterase-inhibiting pesticides on non-target wildlife in irrigated crops,” Ecol. Modell., vol. 210, no. 1–2, pp. 179–192, 2008. [12] T. Gong, R. Liu, Z. Zuo, Y. Che, H.-L. Yu, C. Song, and C. Yang, “Metabolic Engineering of Pseudomonas putida KT2440 for Complete Mineralization of Methyl Parathion and γ-Hexachlorocyclohexane,” ACS Synth. Biol., vol. 5, no. 5, pp. 434–442, May 2016. [13] G. Moussavi, H. Hosseini, and A. Alahabadi, “The investigation of diazinon pesticide removal from contaminated water by adsorption onto NH4Cl-induced activated carbon,” Chem. Eng. J., vol. 214, pp. 172–179, 2013. [14] H. El Bakouri, J. Usero, J. Morillo, R. Rojas, and A. Ouassini, “Drin pesticides removal from aqueous solutions using acid-treated date stones,” Bioresour. Technol., vol. 100, no. 10, pp. 2676–2684, 2009. [15] K. V Plakas and A. J. Karabelas, “Removal of pesticides from water by NF and RO membranes - A review,” Desalination, vol. 287, pp. 255–265, 2012. [16] S. K. Bhargava, J. Tardio, J. Prasad, K. Föger, D. B. Akolekar, and S. C. Grocott, “Wet Oxidation and Catalytic Wet Oxidation,” Ind. Eng. Chem. Res., vol. 45, no. 4, pp. 1221–1258, 2006. [17] E. Kusvuran, D. Yildirim, F. Mavruk, and M. Ceyhan, “Removal of chloropyrifos ethyl, tetradifon and chlorothalonil pesticide residues from citrus by using ozone,” J. Hazard. Mater., vol. 241–242, pp. 287–300, 2012. [18] R. Saini and P. Kumar, “Simultaneous removal of methyl parathion and chlorpyrifos pesticides from model wastewater using coagulation/flocculation: Central composite design,” J. Environ. Chem. Eng., vol. 4, no. 1, pp. 673–680, 2016. [19] L. Zheng, F. Pi, Y. Wang, H. Xu, Y. Zhang, and X. Sun, “Photocatalytic degradation of Acephate, Omethoate, and Methyl parathion by Fe3O4@SiO2@mTiO2 nanomicrospheres,” J. Hazard. Mater., vol. 315, pp. 11–22, Sep. 2016. [20] F. I. Hai, O. Modin, K. Yamamoto, K. Fukushi, F. Nakajima, and L. D. Nghiem, “Pesticide removal by a mixed culture of bacteria and white-rot fungi,” J. Taiwan Inst. Chem. Eng., vol. 43, no. 3, pp. 459–462, 2012. [21] J. G. Carriazo, M. Moreno-Forero, R. A. Molina, and S. Moreno, “Incorporation of titanium and titanium-iron species inside a smectite-type mineral for photocatalysis,” Appl. Clay Sci., vol. 50, no. 3, pp. 401–408, 2010. [22] J. Carriazo, E. Guélou, J. Barrault, J. M. Tatibouët, R. Molina, and S. Moreno, “Catalytic wet peroxide oxidation of phenol by pillared clays containing Al-Ce-Fe,” Water Res., vol. 39, no. 16, pp. 3891–3899, 2005. [23] G. N. Rodrigues, N. Alvarenga, B. Vacondio, S. P. de Vasconcellos, M. R. Z. Passarini, M. H. R. Seleghim, and A. L. M. Porto, “Biotransformation of methyl parathion by marine-derived fungi isolated from ascidian Didemnum ligulum,” Biocatal. Agric. Biotechnol., vol. 7, pp. 24–30, 2016. [24] R. Li, C. Yang, H. Chen, G. Zeng, G. Yu, and J. Guo, “Removal of triazophos pesticide from wastewater with Fenton reagent,” J. Hazard. Mater., vol. 167, no. 1–3, pp. 1028–1032, 2009. [25] A. D. Bokare and W. Choi, “Review of iron-free Fenton-like systems for activating H2O2 in advanced oxidation processes,” J. Hazard. Mater., vol. 275, pp. 121–135, 2014. [26] S. Kouraichi, M. El-Hadi Samar, M. Abbessi, H. Boudouh, and A. Balaska, “Pillared clays as catalysts for methyl parathion removal by advanced oxidation processes,” Catal. Sci. Technol., vol. 5, no. 2, pp. 1052–1064, 2015. [27] A. Özcan, Y. Şahin, and M. A. Oturan, “Complete removal of the insecticide azinphos-methyl from water by the electro-Fenton method – A kinetic and mechanistic study,” Water Res., vol. 47, no. 3, pp. 1470–1479, Mar. 2013. [28] C. F. Gromboni, M. Y. Kamogawa, A. G. Ferreira, J. A. N??brega, and A. R. A. Nogueira, “Microwave-assisted photo-Fenton decomposition of chlorfenvinphos and cypermethrin in residual water,” J. Photochem. Photobiol. A Chem., vol. 185, no. 1, pp. 32–37, 2007. [29] J. J. Pignatello and Y. Sun, “Complete oxidation of metolachlor and methyl parathion in water by the photoassisted Fenton reaction,” Water Res., vol. 29, no. 8, pp. 1837–1844, 1995. [30] K. E. O’Shea, S. Beightol, I. Garcia, M. Aguilar, D. V Kalen, and W. J. Cooper, “Photocatalytic decomposition of organophosphonates in irradiated TiO2 suspensions,” J. Photochem. Photobiol. A Chem., vol. 107, no. 1–3, pp. 221–226, 1997. [31] I. K. Konstantinou, T. M. Sakellarides, V. A. Sakkas, and T. A. Albanis, “Photocatalytic Degradation of Selected s-Triazine Herbicides and Organophosphorus Insecticides over Aqueous TiO 2 Suspensions,” Environ. Sci. Technol., vol. 35, no. 2, pp. 398–405, 2001. [32] T. M. Sakellarides, V. a. Sakkas, D. a. Lambropoulou, and T. a. Albanis, “Application of solid-phase microextraction (spme) for photocatalytic studies of fenitrothion and methyl parathion in aqueous TiO 2 suspensions,” Int. J. Environ. Anal. Chem., vol. 84, no. 1–3, pp. 161–172, 2004. [33] A. Sanjuan, G. Aguirre, M. Alvaro, and H. Garcı́a, “2, 4, 6-Triphenylpyrylium ion encapsulated within Y zeolite as photocatalyst for the degradation of methyl parathion,” Water Res., vol. 34, no. 1, pp. 320–326, 2000. [34] E. Moctezuma, E. Leyva, G. Palestino, and H. de Lasa, “Photocatalytic degradation of methyl parathion: Reaction pathways and intermediate reaction products,” J. Photochem. Photobiol. A Chem., vol. 186, no. 1, pp. 71–84, 2007. [35] X. Liao, C. Zhang, Y. Liu, Y. Luo, S. Wu, S. Yuan, and Z. Zhu, “Abiotic degradation of methyl parathion by manganese dioxide: Kinetics and transformation pathway,” Chemosphere, vol. 150, pp. 90–96, 2016. [36] M. Henych, J., Štengl, V., Slušná, M., Grygar, T. M., Janoš, P., Kuráň, P., & Štastný, “Degradation of organophosphorus pesticide parathion methyl on nanostructured titania-iron mixed oxides,” Appl. Surf. Sci., vol. 344, pp. 9–16, 2015. [37] P. Janoš, P. Kuráň, V. Pilařová, J. Trögl, M. Šťastný, O. Pelant, J. Henych, S. Bakardjieva, O. Životský, M. Kormunda, K. Mazanec, and M. Skoumal, “Magnetically separable reactive sorbent based on the CeO2/γ-Fe2O3 composite and its utilization for rapid degradation of the organophosphate pesticide parathion methyl and certain nerve agents,” Chem. Eng. J., vol. 262, pp. 747–755, Feb. 2015. [38] J. G. Carriazo, L. F. Bossa-Benavides, and E. Castillo, “Actividad catalítica de metales de transición en la descomposición de peróxido de hidrógeno,” Quim. Nova, vol. 35, no. 6, pp. 1101–1106, 2012. [39] J. M. Tatibouët, E. Guélou, and J. Fournier, “Catalytic oxidation of phenol by hydrogen peroxide over a pillared clay containing iron. Active species and pH effect,” Top. Catal., vol. 33, no. 1–4, pp. 225–232, 2005. [40] A. M. Carrillo and J. G. Carriazo, “Cu and Co oxides supported on halloysite for the total oxidation of toluene,” Appl. Catal. B Environ., vol. 164, pp. 443–452, 2015.
dc.rightsCopyright (c) 2017 Tecno Lógicasen-US
dc.sourceTecnoLógicas; Vol. 19 No. 37 (2016); 13-28en-US
dc.sourceTecnoLógicas; Vol. 19 Núm. 37 (2016); 13-28es-ES
dc.source2256-5337
dc.source0123-7799
dc.subjectMethyl parathion degradationen-US
dc.subjectiron oxideen-US
dc.subjectcobalt oxideen-US
dc.subjectcopper oxideen-US
dc.subjectheterogeneous catalysts.en-US
dc.subjectDegradación de metilparatiónes-ES
dc.subjectóxido de hierroes-ES
dc.subjectóxido de cobaltoes-ES
dc.subjectóxido de cobrees-ES
dc.subjectcatalizadores heterogéneos.es-ES
dc.titleHomogeneous and heterogeneous catalysts of Fe3+, Co2+ and Cu2+ for the degradation of methyl parathion in diluted aqueous mediumen-US
dc.titleCatalizadores homogéneos y heterogéneos de Fe3+, Co2+ y Cu2+ para la degradación de metilparatión en medio acuoso diluidoes-ES
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typeResearch Papersen-US
dc.typeArtículos de investigaciónes-ES


Ficheros en el ítem

FicherosTamañoFormatoVer

No hay ficheros asociados a este ítem.

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem