TY - JOUR
T1 - Biofouling of reverse osmosis membranes
T2 - Role of biofilm-enhanced osmotic pressure
AU - Herzberg, Moshe
AU - Elimelech, Menachem
N1 - Funding Information:
This research was made possible by the WaterCAMPWS, a Science and Technology Center of Advanced Materials for the Purification of Water with Systems under the National Science Foundation agreement number CTS-0120978, and by a postdoctoral fellowship supplied by the United States-Israel Binational Agricultural Research and Development (BARD) fund. We also thank S. Molin from the Technical University of Denmark for providing us with Pseudomonas aeruginosa PA01 AH298 and Joseph S. Wolenski from the Molecular, Cellular, and Developmental Biology Department at Yale University for his help with the LSCM.
PY - 2007/5/31
Y1 - 2007/5/31
N2 - A bench-scale investigation of RO biofouling with Pseudomonas aeruginosa PA01 was conducted in order to elucidate the mechanisms governing the decline in RO membrane performance caused by cell deposition and biofilm growth. A sharp decline in permeate water flux and a concomitant increase in salt passage were observed following the inoculation of the RO test unit with a late exponential culture of P. aeruginosa PA01 under enhanced biofouling conditions. The decrease in permeate flux and salt rejection is attributed to the growth of a biofilm comprised of bacterial cells and their self-produced extracellular polymeric substances (EPS). Biofilm growth dynamics on the RO membrane surface are observed using confocal microscopy, where active cells, dead cells, and EPS are monitored. We propose that the biofilm deteriorates membrane performance by increasing both the trans-membrane osmotic pressure and hydraulic resistance. By comparing the decrease in permeate flux and salt rejection upon fouling with dead cells of P. aeruginosa PA01 and upon biofilm growth on the membrane surface, we can distinguish between these two fouling mechanisms. Bacterial cells on the membrane hinder the back diffusion of salt, which results in elevated osmotic pressure on the membrane surface, and therefore a decrease in permeate flux and salt rejection. On the other hand, EPS contributes to the decline in membrane water flux by increasing the hydraulic resistance to permeate flow. Scanning electron microscope (SEM) images of dead cells and biofilm further support these proposed mechanisms. Biofilm imaging reveals an opaque EPS matrix surrounding P. aeruginosa PA01 cells that could provide hydraulic resistance to permeate flux. In contrast, SEM images taken after fouling runs with dead cells reveal a porous cake layer comprised of EPS-free individual cells that is likely to provide negligible resistance to permeate flow compared to the RO membrane resistance. We conclude that "biofilm-enhanced osmotic pressure" plays a dominant role in RO biofouling.
AB - A bench-scale investigation of RO biofouling with Pseudomonas aeruginosa PA01 was conducted in order to elucidate the mechanisms governing the decline in RO membrane performance caused by cell deposition and biofilm growth. A sharp decline in permeate water flux and a concomitant increase in salt passage were observed following the inoculation of the RO test unit with a late exponential culture of P. aeruginosa PA01 under enhanced biofouling conditions. The decrease in permeate flux and salt rejection is attributed to the growth of a biofilm comprised of bacterial cells and their self-produced extracellular polymeric substances (EPS). Biofilm growth dynamics on the RO membrane surface are observed using confocal microscopy, where active cells, dead cells, and EPS are monitored. We propose that the biofilm deteriorates membrane performance by increasing both the trans-membrane osmotic pressure and hydraulic resistance. By comparing the decrease in permeate flux and salt rejection upon fouling with dead cells of P. aeruginosa PA01 and upon biofilm growth on the membrane surface, we can distinguish between these two fouling mechanisms. Bacterial cells on the membrane hinder the back diffusion of salt, which results in elevated osmotic pressure on the membrane surface, and therefore a decrease in permeate flux and salt rejection. On the other hand, EPS contributes to the decline in membrane water flux by increasing the hydraulic resistance to permeate flow. Scanning electron microscope (SEM) images of dead cells and biofilm further support these proposed mechanisms. Biofilm imaging reveals an opaque EPS matrix surrounding P. aeruginosa PA01 cells that could provide hydraulic resistance to permeate flux. In contrast, SEM images taken after fouling runs with dead cells reveal a porous cake layer comprised of EPS-free individual cells that is likely to provide negligible resistance to permeate flow compared to the RO membrane resistance. We conclude that "biofilm-enhanced osmotic pressure" plays a dominant role in RO biofouling.
KW - Biofilm
KW - Biofilm-enhanced osmotic pressure
KW - Biofouling
KW - Cake-enhanced osmotic
KW - EPS
KW - Fouling
KW - P. aeruginosa
UR - http://www.scopus.com/inward/record.url?scp=34247167033&partnerID=8YFLogxK
U2 - 10.1016/j.memsci.2007.02.024
DO - 10.1016/j.memsci.2007.02.024
M3 - Article
AN - SCOPUS:34247167033
SN - 0376-7388
VL - 295
SP - 11
EP - 20
JO - Journal of Membrane Science
JF - Journal of Membrane Science
IS - 1-2
ER -