TY - JOUR
T1 - Modification of a polypropylene feed spacer with metal oxide-thin film by chemical bath deposition for biofouling control in membrane filtration
AU - Thamaraiselvan, Chidambaram
AU - Carmiel, Yacov
AU - Eliad, Gary
AU - Sukenik, Chaim N.
AU - Semiat, Raphael
AU - Dosoretz, Carlos G.
N1 - Funding Information:
This work was funded by the KAMIN program, Ministry of Commerce, Israel and supported in part at the Technion by the Technion-Guangdong Fellowship , Israel. The Russell Berrie Nanotechnology Institute (RBNI) at the Technion, Israel and the Helmsley Charitable Trust, USA are gratefully acknowledged for their support.
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2019/3/1
Y1 - 2019/3/1
N2 - 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.
AB - 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.
KW - Antibacterial feed spacer
KW - Chemical bath deposition
KW - Crystalline ZnO nanorods
KW - Nanoparticles seeding layer
KW - Superhydrophobic coating
UR - http://www.scopus.com/inward/record.url?scp=85058670652&partnerID=8YFLogxK
U2 - 10.1016/j.memsci.2018.12.033
DO - 10.1016/j.memsci.2018.12.033
M3 - Article
AN - SCOPUS:85058670652
VL - 573
SP - 511
EP - 519
JO - Journal of Membrane Science
JF - Journal of Membrane Science
SN - 0376-7388
ER -