Now showing 1 - 4 of 4
No Thumbnail Available
Disinfection of a polyamide nanofiltration membrane using ethanol
2013-12-15, Heffernan, Rory, Correia-Semião, Andrea Joana C., Desmond, P., Cao, Huayu, Safari, Ashkan, Habimana, Olivier, Casey, Eoin
It is imperative that nanofiltration membranes are disinfected before they are used for laboratory-scale bacterial adhesion or biofouling experiments, yet currently no suitable disinfection protocol exists. This study aimed to determine if an ethanol treatment at a minimum inhibitory concentration (MIC) could be used to effectively disinfect nanofiltration membranes without altering membrane properties which could affect research. Two strains of bacteria, Pseudomonas fluorescens and Staphylococcus sp., were exposed to a range of ethanol concentrations to determine the MIC required for a 4log10 reduction in bacteria. In parallel, ethanol's effects on the filtration, surface and mechanical properties of a Dow Filmtec NF90 membrane were analysed. A 1.5 hour treatment with 40% ethanol was shown to effectively disinfect the membrane without significantly affecting any of the membranes properties tested. This treatment protocol can now be safely used to disinfect the studied membrane prior to bacterial adhesion or biofouling experiments. This study also acts as a guideline for researchers using other membranes to determine a suitable disinfection protocol for their needs.
No Thumbnail Available
A physical impact of organic fouling layers on bacterial adhesion during nanofiltration
2014-12-15, Heffernan, Rory, Habimana, Olivier, Correia-Semião, Andrea Joana C., Cao, Huayu, Safari, Ashkan, Casey, Eoin
Organic conditioning films have been shown to alter properties of surfaces, such as hydrophobicity and surface free energy. Furthermore, initial bacterial adhesion has been shown to depend on the conditioning film surface properties as opposed to the properties of the virgin surface. For the particular case of nanofiltration membranes under permeate flux conditions, however, the conditioning film thickens to form a thin fouling layer. This study hence sought to determine if a thin fouling layer deposited on a nanofiltration membrane under permeate flux conditions governed bacterial adhesion in the same manner as a conditioning film on a surface. Thin fouling layers (less than 50 μm thick) of humic acid or alginic acid were formed on Dow Filmtec NF90 membranes and analysed using Atomic Force Microscopy (AFM), confocal microscopy and surface energy techniques. Fluorescent microscopy was then used to quantify adhesion of Pseudomonas fluorescens bacterial cells onto virgin or fouled membranes under filtration conditions.It was found that instead of adhering on or into the organic fouling layer, the bacterial cells penetrated the thin fouling layer and adhered directly to the membrane surface underneath. Contrary to what surface energy measurements of the fouling layer would indicate, bacteria adhered to a greater extent onto clean membranes (24 ± 3% surface coverage) than onto those fouled with humic acid (9.8 ± 4%) or alginic acid (7.5 ± 4%). These results were confirmed by AFM measurements which indicated that a considerable amount of energy (10−7 J/μm) was dissipated when attempting to penetrate the fouling layers compared to adhering onto clean NF90 membranes (10−15 J/μm). The added resistance of this fouling layer was thusly seen to reduce the number of bacterial cells which could reach the membrane surface under permeate conditions. This research has highlighted an important difference between fouling layers for the particular case of nanofiltration membranes under permeate flux conditions and surface conditioning films which should be considered when conducting adhesion experiments under filtration conditions. It has also shown AFM to be an integral tool for such experiments.
No Thumbnail Available
Understanding particle deposition kinetics on NF membranes: A focus on micro-beads & membrane interactions at different environmental conditions
2015-02-01, Cao, Huayu, Habimana, Olivier, Correia-Semião, Andrea Joana C., Allen, Ashley, Heffernan, Rory, Casey, Eoin
The significance of nanofiltration membrane surface properties when interacting with microbeads with and without permeate flux was investigated. This was achieved by characterising the surface tension and zeta potential of micro-beads and NF90 membranes to determine the colloid–membrane interaction forces. Dynamic adhesion assays under different ionic strengths (0.1 M and 0.01 M) and pH (5, 7, and 9) were conducted. Experimental results showed that at high ionic strength, pH does not have a significant effect on adhesion rates, while at low ionic strength the adhesion rate increased at pH 7 (4.56 s−1 cm−2) compared to pH 5 and pH 9, with rates of 2.69 and 3.66 s−1 cm−2 respectively. A model was devised to predict colloidal adhesion onto membranes under increasing permeate flux conditions, taking into account all interaction forces. Model predictions indicate that drag force overwhelms all other colloid–membrane interaction forces when the permeate flux increases to 7.2 L h−1 m−2. This study suggests that altering membrane surface properties for the prevention of fouling may be limited in its success as an antifouling strategy.
No Thumbnail Available
The importance of laboratory water quality for studying initial bacterial adhesion during NF filtration processes
2013-05-15, Correia-Semião, Andrea Joana C., Habimana, Olivier, Cao, Huayu, Heffernan, Rory, Safari, Ashkan, Casey, Eoin
Biofouling of nanofiltration (NF) and reverse osmosis (RO) membranes for water treatment has been the subject of increased research effort in recent years. A prerequisite for undertaking fundamental experimental investigation on NF and RO processes is a procedure called compaction. This involves an initial phase of clean water permeation at high pressures until a stable permeate flux is reached. However water quality used during the compaction process may vary from one laboratory to another. The aim of this study was to investigate the impact of laboratory water quality during compaction of NF membranes. A second objective was to investigate if the water quality used during compaction influences initial bacterial adhesion. Experiments were undertaken with NF270 membranes at 15 bar for permeate volumes of 0.5L, 2L, and 5L using MilliQ, deionized or tap water. Membrane autopsies were performed at each permeation point for membrane surface characterisation by contact angle measurements, profilometry, and scanning electron microscopy. The biological content of compacted membranes was assessed by direct epi-fluorescence observation following nucleic acid staining. The compacted membranes were also employed as substrata for monitoring the initial adhesion of Ps. fluorescens under dynamic flow conditions for 30 minutes at 5 minutes intervals. Compared to MilliQ water, membrane compaction using deionized and tap water led to decreases in permeate flux, increase in surface hydrophobicity and led to significant buildup of a homogenous fouling layer composed of both living and dead organisms (>10⁶cells.cm−2). Subsequent measurements of bacterial adhesion resulted in cell loadings of 0.2×10⁵, 1.0×10⁵cells×cm−2 and 2.6×10⁵ cells.cm−2 for deionized, tap water and MilliQ water, respectively. These differences in initial cell adhesion rates demonstrate that choice of laboratory water can significantly impact the results of bacterial adhesion on NF membranes. Standardized protocols are therefore needed for the fundamental studies of bacterial adhesion and biofouling formation on NF and RO membrane. This can be implemented by first employing pure water during all membrane compaction proceduresand for the modelled feed solutions used in the experiment.