Management of table olive processing wastewater by an osmotic membrane bioreactor process

[EN] The management of fermentation brines from the table olive processing is very complex due to its characteristics: high salinity and high organic matter concentration including phenolic compounds, which behave as slow degradable compounds when a biological process is performed. In this work, the...

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Detalles Bibliográficos
Autores: Lujan Facundo, Maria Jose|||0000-0001-6871-0584, Mendoza Roca, José Antonio, Soler Cabezas, José Luis|||0000-0002-4610-3369, Bes-Piá, M.A.|||0000-0001-8005-7450, Vincent Vela, Maria Cinta|||0000-0001-8493-0165, Cuartas Uribe, Beatriz Elena|||0000-0003-2835-900X, Pastor-Alcaniz, L.
Tipo de recurso: artículo
Fecha de publicación:2020
País:España
Institución:Universitat Politècnica de València (UPV)
Repositorio:RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
Idioma:inglés
OAI Identifier:oai:riunet.upv.es:10251/177256
Acceso en línea:https://riunet.upv.es/handle/10251/177256
Access Level:acceso abierto
Palabra clave:Forward osmosis
Osmotic membrane bioreactor
Wastewater treatment
INGENIERIA QUIMICA
Descripción
Sumario:[EN] The management of fermentation brines from the table olive processing is very complex due to its characteristics: high salinity and high organic matter concentration including phenolic compounds, which behave as slow degradable compounds when a biological process is performed. In this work, the management of these effluents by an osmotic membrane bioreactor has been assessed. This technique combines a biological reactor with forward osmosis membranes. For the study, a laboratory plant consisting of 1 L reactor and a forward osmosis module equipped with a membrane of 42 cm(2) of active surface has been used. Fermentation brine from table olive processing was fed to the system both as draw solution to set out the driving force for the membrane process and as a part of the feed to the reactor, mixing it with municipal wastewater. The experiments were carried out at a constant feed to microorganism ratio of 0.4 g COD.g SS-1.d(-1). Results indicated that the hypersaline effluent was able to produce the needed driving force by the process. Permeate fluxes ranged between 1 and 1.5 L.m(-2).h(-1) after the flux decay of the first operation days. Concerning the biological reaction, it has to be highlighted that phenols were eliminated after 24 days. Until that day, the biological process was jeopardized due to the quick increase of the conductivity in the reactor (ranging between 30 and 35 mS.cm(-1)), which was caused not only by the salinity of the influent but also by the reverse salt flux phenomenon. Soluble microbial products and extracted extracellular polymeric substances also increased in the reactor during the start-up.