The impact of hydrophobic coating on the performance of carbon nanotube bucky-paper membranes in membrane distillation
Research Highlights
► PTFE/carbon nanotube bucky-papers composites were fabricated by sputtering PTFE on top of a performed self-supporting bucky-paper. ► The samples were characterized and the membrane permeability performance tested in a direct contact membrane distillation rig.
Introduction
The engineering of carbon nanotube (CNT) based membranes has been investigated over the past 10 years as a mean to overcome global water stress and shortage [1], [2], [3]. Several approaches have been undertaken to benefit from the unique CNT properties and fabricate membranes exhibiting enhanced permeability and selectivity [4], [5], [6], [7] compared to existing membranes used in reverse osmosis [8], [9], [10], nanofiltration [11], ultrafiltration [12], pervaporation [13], [14], [15] or capacitive deionisation [16]. Selective ion transport across aligned CNT composites [17] was demonstrated and enhanced flux across pristine CNT composite membrane [13], [18] were encouraging steps to further pursue their use in separation. An alternative low energy route to desalinate water is Direct Contact Membrane Distillation (DCMD) where a membrane is used as a separation barrier between two streams of water at different temperature. The hot saline solution contacts the membrane on one side and water vapour, generated from the vapour pressure gradient across the air gap is transported across the membrane before being condensed on the cold side.
Suitable membranes for DCMD [19] need to be porous, hydrophobic and thin to facilitate the water vapour permeation while preventing direct bridges across the membrane air-gap [20]. Bucky-papers (BP) [21], [22], non-woven of entangled CNTs, exhibit high porosity and hydrophobicity [23] and previous work showed that CNT composite Bucky-papers (BP) could be successfully engineered and used as membranes for water desalination by direct contact membrane distillation [24], [25].
In this paper CNT BPs were coated with poly(tetra-fluoro-ethylene) by sputtering. Extensive properties characterisation, such as contact angle, pore size distribution and porosity, were performed on the membranes which were tested in a DCMD rig for desalination of saline solution. The composite membranes were compared with non coated BP and with commercial PTFE membranes.
Section snippets
Materials and method
CNTs grown by chemical vapor deposition using an established method reported elsewhere [26], [27] typically exhibited outer diameters and lengths of respectively 10–15 nm and 200–300 μm. The CNTs were (i) dispersed in analytical grade propan-2-ol and sonicated (5 times for 10 min at 150 W) to achieve homogeneous suspensions [24], (ii) filtered under vacuum and (iii) dried overnight in a vacuum oven (at 80 °C and − 20 kPa) to form BPs that could be peeled off to form self-supporting BP. BPs were coated
Membrane characterisation
SEM imaging revealed that the PTFE coating formed a thin continuous and porous film at the surface of the BP as clearly seen in Fig. 1-C. Fig. 1-D shows a high magnification SEM of the nanotube composite after sputtering. The membrane surface did not seem to be drastically changed and neither blockages nor polymer agglomerates were visible on the images. The measurement of the CNT diameters before and after coating confirmed the measurement of the PTFE thickness on a glass slide reference
Conclusion
PTFE coated carbon nanotube BPs were processed and successfully tested as potential membranes in DCMD. They exhibited improved properties compared to both their untreated counter parts and to commercial membranes. The difference was attributed to the higher hydrophobicity of the smooth surface and to an increased porosity compared to the PTFE membranes making of those membranes very promising structures for use as separation membranes in membrane distillation.
Acknowledgements
The authors would like to acknowledge RMIT for access to their sputtering facilities and to Dr. Yen Truong for granting us the access to both porometer and goniometer. We thank the CSIRO Materials Science and Engineering and Victoria University for the financial support. They also thank Sergey Rubanov from Bio 21 Institute for his expert advice on SEM microscopy.
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