47 research outputs found
Extracellular proteins of Trametes hirsuta st. 072 induced by copper ions and a lignocellulose substrate
Strategies to enhance the removal of the persistent pharmaceutically active compound carbamazepine by membrane bioreactors
Lignin peroxidase isozymes from phanerochaete chrysosporium can be enzymatically dephosphorylated
Effect of Permeate Drag Force on the Development of a Biofouling Layer in a Pressure-Driven Membrane Separation System▿
The effect of permeate flux on the development of a biofouling layer on cross-flow separation membranes was studied by using a bench-scale system consisting of two replicate 100-molecular-weight-cutoff tubular ultrafiltration membrane modules, one that allowed flow of permeate and one that did not (control). The system was inoculated with Pseudomonas putida S-12 tagged with a red fluorescent protein and was operated using a laminar flow regimen under sterile conditions with a constant feed of diluted (1:75) Luria-Bertani medium. Biofilm development was studied by using field emission scanning electron microscopy and confocal scanning laser microscopy and was subsequently quantified by image analysis, as well as by determining live counts and by permeate flux monitoring. Biofilm development was highly enhanced in the presence of permeate flow, which resulted in the buildup of complex three-dimensional structures on the membrane. Bacterial transport toward the membrane by permeate drag was found to be a mechanism by which cross-flow filtration contributes to the buildup of a biofouling layer that was more dominant than transport of nutrients. Cellular viability was found to be not essential for transport and adhesion under cross-flow conditions, since the permeate drag overcame the effect of bacterial motility
Modification of a polypropylene feed spacer with metal oxide-thin film by chemical bath deposition for biofouling control in membrane filtration
© 2018 Elsevier B.V. Surface modification of polypropylene feed spacers typical of spiral wound membrane modules was studied by generation of crystalline ZnO nanorods. A seeding layer made by deposition of ZnO nanoparticles (20–40–60 nm diameter) from aqueous dispersions served as nucleation centers for crystallization. A uniform layer of ZnO nanorods was grown on the seeding layer by chemical bath deposition from a zinc acetate solution. Biocidal activity was estimated by antibacterial tests in static liquid culture against Escherichia coli and antibiofouling tests in flow-through/cross-flow mode against a mixture of Pseudomonas fluorescens and Bacillus subtilis. Best biocidal activity was displayed by 20 nm ZnO particles, suggesting a tradeoff between surface coverage, roughness and particle size. Although the seed layer itself displayed acceptable antibacterial activity, a marked improvement was achieved by the nanorods, proving that the morphology of the deposition layer was involved in the antibacterial mechanism. Antibiofouling activity was further improved by superhydrophobic over-coating of the nanorods with octadecyl-phosphonic acid. Modified spacers reduced permeate flux decay by at least 40% compared to controls. The enhanced antibiofouling activity of crystalline ZnO nanorods, compared with amorphous ZnO nanoparticles, can be explained by a combination of the abrasive surface of the crystalline nanorods, hydrophobic repulsion and cumulative oxidation