Remoção de microcistina-LR de água utilizando coagulação com reagente de Fenton, floculação, decantação e filtração seguido de carvão ativado granular

Detalhes bibliográficos
Ano de defesa: 2012
Autor(a) principal: Buriti, Josué da Silva lattes
Orientador(a): Lopes, Wilton Silva
Banca de defesa: Julio, Marcelo de lattes, Ceballos, Beatriz Suzana Ovruski de lattes
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Estadual da Paraíba
Programa de Pós-Graduação: Programa de Pós-Graduação em Ciência e Tecnologia Ambiental - PPGCTA
Departamento: Tecnologia Ambiental
Pró-Reitoria de Pós-Graduação e Pesquisa - PRPGP
País: BR
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: https://repositorio.uepb.edu.br/handle/123456789/72187
Resumo: This study aimed to evaluate at bench-scale the removal of microcystin-LR from water for public supply using Fenton's reagent, coagulation, flocculation, sedimentation and filtration by columns of granular activated carbon (GAC). The water used in this study was prepared by adding 20 mL of microcystin-LR extract (obtained from a pure culture of Microcystis aeruginosa after three consecutive freeze / thaw cycles), in 1L of untreated water from the Acauã reservoir and which corresponded to a concentration of microcystin-LR of aproximately 19 µg.L . The experiments were conducted in three stages. The first step was to determine the best conditions for coagulation obtained via diagrams of coagulation based on remaining turbidity and apparent colour after treatment with Fenton's reagent at concentrations between 5 mg.L-1 and 100 mg.L-1 f eSO4.7H2O and 1.83 mg.L-1 to 36.70 mg.L of H2O and pH varying between 3 and 9 at a settling time of 5 min. In the second stage the fastest sedimentation time was determined after coagulation based on the control parameters of remaining turbidity, apparent colour and microcystin-LR concentration. The third stage evaluated the adsorption of microcystin-LR in columns of GAC (particle size between 1.40 mm and 0.42 mm) after the conditions defined in steps I and II. The GAC columns were constructed from PVC tubing with an internal diameter of 21 mm and a functional height of GAC of 15 cm and 20 cm, corresponding to two different contact times. The fixed flow rate for each GAC column was 2 L.h2-1. The optimum conditions for coagulation were 15 mg.L FeSO4.7H2O and 5.5 g.L-1 H2O, at pH 8.4 and coagulation and sedimentation times of 15 min. After coagulation, flocculation and sedimentation turbidity decreased from 5.8 to 3.0 uT, apparent color of 115 uH to 81 uH and a reduction in microcystinLR concentration from 18.52 µg.L2-1 to 9.59 µg.L-1, with percentage removals of 48%, 30% and 48%, respectively. Break-through occurred in the shorter length column of GAC with the shorter contact time (CC1) after 2 hours of operation, resulting in a smaller q e (1.85 μg.g-1) and higher usage rate (3.82 g.L-1) compared o the GAC column with the greater contact time (CC2), with a break-through after 6 hours operation. Thus the longer GAC column (CC2) gave a better performance both in terms of q e (4.15 μg.g-1) and rate of use (1.70 g.L-1), ensuring effluent oncentration below the maximum allowable value of 1 µg.L-1 required by Ordinance 2914/11, Ministry of Health, with a longer operational life and an economy in GAC usage.
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spelling 2015-09-25T12:19:41Z2026-02-25T12:46:36Z2012-09-122012-08-27BURITI, Josué da Silva. Removal of microcystin-LR from water using Fenton s reagent coagulation, flocculation, sedimentation and filtration followed by granular activated carbon. 2012. 89 f. Dissertação (Mestrado em Tecnologia Ambiental) - Universidade Estadual da Paraíba, Campina Grande, 2012.https://repositorio.uepb.edu.br/handle/123456789/7218724004014005P9This study aimed to evaluate at bench-scale the removal of microcystin-LR from water for public supply using Fenton's reagent, coagulation, flocculation, sedimentation and filtration by columns of granular activated carbon (GAC). The water used in this study was prepared by adding 20 mL of microcystin-LR extract (obtained from a pure culture of Microcystis aeruginosa after three consecutive freeze / thaw cycles), in 1L of untreated water from the Acauã reservoir and which corresponded to a concentration of microcystin-LR of aproximately 19 µg.L . The experiments were conducted in three stages. The first step was to determine the best conditions for coagulation obtained via diagrams of coagulation based on remaining turbidity and apparent colour after treatment with Fenton's reagent at concentrations between 5 mg.L-1 and 100 mg.L-1 f eSO4.7H2O and 1.83 mg.L-1 to 36.70 mg.L of H2O and pH varying between 3 and 9 at a settling time of 5 min. In the second stage the fastest sedimentation time was determined after coagulation based on the control parameters of remaining turbidity, apparent colour and microcystin-LR concentration. The third stage evaluated the adsorption of microcystin-LR in columns of GAC (particle size between 1.40 mm and 0.42 mm) after the conditions defined in steps I and II. The GAC columns were constructed from PVC tubing with an internal diameter of 21 mm and a functional height of GAC of 15 cm and 20 cm, corresponding to two different contact times. The fixed flow rate for each GAC column was 2 L.h2-1. The optimum conditions for coagulation were 15 mg.L FeSO4.7H2O and 5.5 g.L-1 H2O, at pH 8.4 and coagulation and sedimentation times of 15 min. After coagulation, flocculation and sedimentation turbidity decreased from 5.8 to 3.0 uT, apparent color of 115 uH to 81 uH and a reduction in microcystinLR concentration from 18.52 µg.L2-1 to 9.59 µg.L-1, with percentage removals of 48%, 30% and 48%, respectively. Break-through occurred in the shorter length column of GAC with the shorter contact time (CC1) after 2 hours of operation, resulting in a smaller q e (1.85 μg.g-1) and higher usage rate (3.82 g.L-1) compared o the GAC column with the greater contact time (CC2), with a break-through after 6 hours operation. Thus the longer GAC column (CC2) gave a better performance both in terms of q e (4.15 μg.g-1) and rate of use (1.70 g.L-1), ensuring effluent oncentration below the maximum allowable value of 1 µg.L-1 required by Ordinance 2914/11, Ministry of Health, with a longer operational life and an economy in GAC usage.Este trabalho teve como objetivo avaliar em escala de bancada a remoção de microcistina-LR de água destinada ao abastecimento público utilizando coagulação com reagente de Fenton, floculação, decantação e filtração seguido de colunas de carvão ativado granular (CAG). A água de estudo foi preparada pela adição de 20 mL de extrato de microcistina-LR (após congelamento/descongelamento por três vezes consecutivas da cultura pura de Microcystis aeruginosa) em 1 L de água bruta do reservatório de Acauã, que correspondeu a concentração de microcistina-LR em torno de 19 μg.L-1 . O experimento foi realizado em três etapas. Na primeira etapa foi definida a melhor condição de coagulação através de diagramas de coagulação para turbidez remanescente e cor aparente remanescente com concentração de reagente de Fenton entre 5 mg.L-1 - 100 mg.L-1 de FeSO4.7H2O e 1,83 mg.L de H2O para pH de coagulação entre 3 e 9 com tempo de sedimentação de 5 min. Na segunda etapa foi definido o melhor tempo de sedimentação conforme as condições de coagulação estabelecidas na etapa I e os parâmetros de controle foram turbidez remanescente, cor aparente remanescente e microcistina-LR remanescente. Na terceira etapa foi avaliada a adsorção da microcistina-LR em colunas de CAG (granulometria entre 1,40 mm e 0,42 mm) utilizando as condições definidas nas etapas I e II. As colunas de CAG foram construídas com tubos de PVC com diâmetro interno de 21 mm e altura útil de CAG de 15 cm e 20 cm, correspondendo a dois tempos de contato distintos. A vazão fixada para cada coluna de CAG foi de 2 L.h2-1-1. A melhor condição de coagulação foi 15 mg.L de FeSO4.7H2O; 5,5 mg.L-1 de H2O , pH de coagulação de 8,4 e tempo de sedimentação de 15 min. Após a coagulação, floculação e sedimentação a turbidez reduziu de 5,8 uT a 3,0 uT, cor aparente de 115 uH a 81 uH e concentração de microcistina-LR de 18,52 µg.L-12 a 9,59 µg.L-1, com percentuais de remoção de 48%, 30% e 48%, respectivamente. O transpasse na coluna de CAG de menor tempo de contato (CC1) ocorreu após 2 horas de funcionamento do sistema, refletindo em menor qe (1,85 μg.g-) e maior taxa de uso (3,82 g.L-1) quando comparada a coluna de CAG de maior tempo de contato (CC2), que ocorreu o transpasse após 6 horas de funcionamento do sistema, a qual apresentou melhor desempenho tanto em relação ao qe (4,15 g.g-1) como em relação a taxa de uso (1,70 g.L), garantindo efluente com concentração inferior ao valor máximo permitido de 1 µg.L exigido pela Portaria 2914/11 do Ministério da Saúde por mais tempo e utilizando uma menor quantidade de CAG. - 36,70 mg.LCoordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESapplication/pdfUniversidade Estadual da ParaíbaPrograma de Pós-Graduação em Ciência e Tecnologia Ambiental - PPGCTAUEPBBRTecnologia AmbientalPró-Reitoria de Pós-Graduação e Pesquisa - PRPGPWater treatmentSystem for water supplyMicrocystin-LRCNPQTratamento de águaSistema de abastecimento de águaMicrocistina-LRRemoção de microcistina-LR de água utilizando coagulação com reagente de Fenton, floculação, decantação e filtração seguido de carvão ativado granularRemoval of microcystin-LR from water using Fenton s reagent coagulation, flocculation, sedimentation and filtration followed by granular activated carboninfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisVieira, Fernando Fernandeshttp://lattes.cnpq.br/1129711375633007Julio, Marcelo dehttp://lattes.cnpq.br/8139895417126415Ceballos, Beatriz Suzana Ovruski dehttp://lattes.cnpq.br/9321950498637802Lopes, Wilton Silvahttp://lattes.cnpq.br/4761006194505552Buriti, Josué da Silvainfo:eu-repo/semantics/openAccessporreponame:Repositório Institucional da Universidade Estadual da Paraíba (UEPB)instname:Universidade Estadual da Paraíba (UEPB)instacron:UEPBORIGINALJosue da Silva Buriti.pdfapplication/pdf1828134https://repositorio.uepb.edu.br/bitstreams/9a0bd2cd-52a7-4dfc-b809-c2d033eb9cb9/download34ba27d07ee2de7c2319fe96621f414cMD51trueAnonymousREADTHUMBNAILJosue da Silva Buriti.pdf.jpgJosue da Silva Buriti.pdf.jpgGenerated Thumbnailimage/jpeg4193https://repositorio.uepb.edu.br/bitstreams/0272526a-1962-460f-9d3a-fb4be672ae1d/download5f11087239af2877a5de1e246d0c676aMD52falseAnonymousREADLICENSElicense.txtlicense.txttext/plain; charset=utf-81324https://repositorio.uepb.edu.br/bitstreams/50eff12a-0d7d-49a4-8e33-2784c3d7c924/downloadea12793326f265c7d8ea2bcdd2c49d6fMD53falseAnonymousREAD123456789/721872026-05-06T11:50:22.611903Zopen.accessoai:repositorio.uepb.edu.br:123456789/72187https://repositorio.uepb.edu.brRepositório InstitucionalPUBhttp://dspace.bc.uepb.edu.br/oai/requestsibuepb@setor.uepb.edu.bropendoar:2026-05-06T11:50:22Repositório Institucional da Universidade Estadual da Paraíba (UEPB) - Universidade Estadual da Paraíba (UEPB)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
dc.title.none.fl_str_mv Remoção de microcistina-LR de água utilizando coagulação com reagente de Fenton, floculação, decantação e filtração seguido de carvão ativado granular
dc.title.alternative.eng.fl_str_mv Removal of microcystin-LR from water using Fenton s reagent coagulation, flocculation, sedimentation and filtration followed by granular activated carbon
title Remoção de microcistina-LR de água utilizando coagulação com reagente de Fenton, floculação, decantação e filtração seguido de carvão ativado granular
spellingShingle Remoção de microcistina-LR de água utilizando coagulação com reagente de Fenton, floculação, decantação e filtração seguido de carvão ativado granular
Buriti, Josué da Silva
Water treatment
System for water supply
Microcystin-LR
CNPQ
Tratamento de água
Sistema de abastecimento de água
Microcistina-LR
title_short Remoção de microcistina-LR de água utilizando coagulação com reagente de Fenton, floculação, decantação e filtração seguido de carvão ativado granular
title_full Remoção de microcistina-LR de água utilizando coagulação com reagente de Fenton, floculação, decantação e filtração seguido de carvão ativado granular
title_fullStr Remoção de microcistina-LR de água utilizando coagulação com reagente de Fenton, floculação, decantação e filtração seguido de carvão ativado granular
title_full_unstemmed Remoção de microcistina-LR de água utilizando coagulação com reagente de Fenton, floculação, decantação e filtração seguido de carvão ativado granular
title_sort Remoção de microcistina-LR de água utilizando coagulação com reagente de Fenton, floculação, decantação e filtração seguido de carvão ativado granular
author Buriti, Josué da Silva
author_facet Buriti, Josué da Silva
author_role author
dc.contributor.advisor-co1.fl_str_mv Vieira, Fernando Fernandes
dc.contributor.advisor-co1Lattes.fl_str_mv http://lattes.cnpq.br/1129711375633007
dc.contributor.referee1.fl_str_mv Julio, Marcelo de
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/8139895417126415
dc.contributor.referee2.fl_str_mv Ceballos, Beatriz Suzana Ovruski de
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/9321950498637802
dc.contributor.advisor1.fl_str_mv Lopes, Wilton Silva
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/4761006194505552
dc.contributor.author.fl_str_mv Buriti, Josué da Silva
contributor_str_mv Vieira, Fernando Fernandes
Julio, Marcelo de
Ceballos, Beatriz Suzana Ovruski de
Lopes, Wilton Silva
dc.subject.eng.fl_str_mv Water treatment
System for water supply
Microcystin-LR
topic Water treatment
System for water supply
Microcystin-LR
CNPQ
Tratamento de água
Sistema de abastecimento de água
Microcistina-LR
dc.subject.cnpq.fl_str_mv CNPQ
dc.subject.por.fl_str_mv Tratamento de água
Sistema de abastecimento de água
Microcistina-LR
description This study aimed to evaluate at bench-scale the removal of microcystin-LR from water for public supply using Fenton's reagent, coagulation, flocculation, sedimentation and filtration by columns of granular activated carbon (GAC). The water used in this study was prepared by adding 20 mL of microcystin-LR extract (obtained from a pure culture of Microcystis aeruginosa after three consecutive freeze / thaw cycles), in 1L of untreated water from the Acauã reservoir and which corresponded to a concentration of microcystin-LR of aproximately 19 µg.L . The experiments were conducted in three stages. The first step was to determine the best conditions for coagulation obtained via diagrams of coagulation based on remaining turbidity and apparent colour after treatment with Fenton's reagent at concentrations between 5 mg.L-1 and 100 mg.L-1 f eSO4.7H2O and 1.83 mg.L-1 to 36.70 mg.L of H2O and pH varying between 3 and 9 at a settling time of 5 min. In the second stage the fastest sedimentation time was determined after coagulation based on the control parameters of remaining turbidity, apparent colour and microcystin-LR concentration. The third stage evaluated the adsorption of microcystin-LR in columns of GAC (particle size between 1.40 mm and 0.42 mm) after the conditions defined in steps I and II. The GAC columns were constructed from PVC tubing with an internal diameter of 21 mm and a functional height of GAC of 15 cm and 20 cm, corresponding to two different contact times. The fixed flow rate for each GAC column was 2 L.h2-1. The optimum conditions for coagulation were 15 mg.L FeSO4.7H2O and 5.5 g.L-1 H2O, at pH 8.4 and coagulation and sedimentation times of 15 min. After coagulation, flocculation and sedimentation turbidity decreased from 5.8 to 3.0 uT, apparent color of 115 uH to 81 uH and a reduction in microcystinLR concentration from 18.52 µg.L2-1 to 9.59 µg.L-1, with percentage removals of 48%, 30% and 48%, respectively. Break-through occurred in the shorter length column of GAC with the shorter contact time (CC1) after 2 hours of operation, resulting in a smaller q e (1.85 μg.g-1) and higher usage rate (3.82 g.L-1) compared o the GAC column with the greater contact time (CC2), with a break-through after 6 hours operation. Thus the longer GAC column (CC2) gave a better performance both in terms of q e (4.15 μg.g-1) and rate of use (1.70 g.L-1), ensuring effluent oncentration below the maximum allowable value of 1 µg.L-1 required by Ordinance 2914/11, Ministry of Health, with a longer operational life and an economy in GAC usage.
publishDate 2012
dc.date.available.fl_str_mv 2012-09-12
dc.date.issued.fl_str_mv 2012-08-27
dc.date.accessioned.fl_str_mv 2015-09-25T12:19:41Z
2026-02-25T12:46:36Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.citation.fl_str_mv BURITI, Josué da Silva. Removal of microcystin-LR from water using Fenton s reagent coagulation, flocculation, sedimentation and filtration followed by granular activated carbon. 2012. 89 f. Dissertação (Mestrado em Tecnologia Ambiental) - Universidade Estadual da Paraíba, Campina Grande, 2012.
dc.identifier.uri.fl_str_mv https://repositorio.uepb.edu.br/handle/123456789/72187
dc.identifier.capesdegreeprogramcode.none.fl_str_mv 24004014005P9
identifier_str_mv BURITI, Josué da Silva. Removal of microcystin-LR from water using Fenton s reagent coagulation, flocculation, sedimentation and filtration followed by granular activated carbon. 2012. 89 f. Dissertação (Mestrado em Tecnologia Ambiental) - Universidade Estadual da Paraíba, Campina Grande, 2012.
24004014005P9
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