4.7 Article

Scalable fabrication of anti-biofouling membranes through 2-aminoimidazole incorporation during polyamide casting

Journal

JOURNAL OF MEMBRANE SCIENCE
Volume 579, Issue -, Pages 151-161

Publisher

ELSEVIER
DOI: 10.1016/j.memsci.2019.02.033

Keywords

Anti-biofouling; Reverse osmosis; Membrane modification; 2-Aminoimidazole; Membrane casting

Funding

  1. National Science Foundation (NSF) Grant Opportunities for Academic Liaison with Industry (GOALI) and Chemical, Bioengineering, Environmental, and Transport Systems (CBET) program [1264690]
  2. NSF Environmental Engineering program [1336532]
  3. Sigma Xi
  4. National Water Research Institute (NWRI)
  5. American Membrane Technology Association (AMTA) Fellowship for Membrane Technology
  6. UNC Graduate School Dissertation Completion Fellowship
  7. US Department of Energy Office of Nuclear Physics [97ER41041, 97ER41033]
  8. National Science Foundation as part of the National Nanotechnology Coordinated Infrastructure (NNCI) [ECCS-1542015]
  9. Directorate For Engineering
  10. Div Of Chem, Bioeng, Env, & Transp Sys [1336532] Funding Source: National Science Foundation

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A proof-of-concept for the fabrication of novel anti-biofouling water purification membranes through the incorporation of a 2-aminoimidazole (2-AI) during membrane casting is presented. 2-AI molecules are known to inhibit biofouling through the disruption of biofilm formation mechanisms, not through the inactivation of bacteria. Three approaches to incorporation were evaluated, adding the 2-AI to either one of the two monomer solutions, (a) m-phenylene diamine or (b) trimesoyl chloride, that polymerize to make a polyamide active layer, or by (c) reacting the active layer with a post-polymerization-2-AI-soak solution. These methods of incorporation are directly translatable to current membrane fabrication practices without the addition of other chemicals aside from the 2-AIs themselves. Results showed that the 2-AI was incorporated into the active layer of the membranes at concentrations (0.16-0.93 M) orders of magnitude higher than what is required for biofilm inhibition (IC50 = 162-420 mu M). The 2-AI membranes significantly (p = 0.002-0.04) inhibited Pseudomonas aeruginosa biofilms (49-90% on average) due to the presence and action of 2-AI, not physico-chemical changes. The 2-AIsoak approach produced membranes that had the most stable incorporation, with no loss of compound during use and cleaning, and the highest biofilm inhibition, at 90% inhibition on average. The incorporation of 2-AI into the membranes decreased water permeability by 26-44% and salt rejection by 1.2-4.3% points, as compared to control membranes. No attempt was made to optimize 2-AI membrane preparation toward minimization of changes in water permeability and salt rejection. Given the substantial biofilm formation inhibition exhibited by the 2-AI membranes, and the limited decrease observed in water permeability and salt rejection, the 2-AI membranes presented in this study support 2-AI incorporation into polyamide active layers as a promising avenue to enhance current water purification membranes.

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