4.4 Article

Poly (N-isopropylacrylamide) microgel based assemblies for organic dye removal from water: microgel diameter effects

Journal

COLLOID AND POLYMER SCIENCE
Volume 290, Issue 11, Pages 1053-1064

Publisher

SPRINGER
DOI: 10.1007/s00396-012-2620-3

Keywords

Water remediation and contamination; Poly (N-isopropylacrylamide)-co-acrylic acid microgel aggregates; Thermoresponsive polymeric materials; Azo dyes; pNIPAm

Funding

  1. University of Alberta (the Department of Chemistry and the Faculty of Science)
  2. Natural Science and Engineering Research Council (NSERC)
  3. Canada Foundation for Innovation (CFI)
  4. Alberta Advanced Education & Technology Small Equipment Grants Program (AET/SEGP)

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Poly (N-isopropylacrylamide)-co-acrylic acid (pNIPAm-co-AAc) microgel based assemblies (aggregates) were synthesized from microgels of various diameters via polymerization of the crosslinker N,N'-methylenebisacrylamide (BIS) in the presence of microgels in solution. We investigated the ability of the respective aggregates to remove the organic, azo dye molecule 4-(2-hydroxy-1-napthylazo) benzenesulfonic acid sodium salt (Orange II) from water at both room and elevated temperatures. The results from the microgel aggregates made from 1.1-mu m-diameter [Parasuraman and Serpe. ACS Applied Materials & Interfaces, 2011] microgels were compared to aggregates synthesized from 321-nm and 1.43-mu m-diameter microgels. Aggregates made from the same size microgels showed increased uptake efficiency as the concentration of BIS in the aggregates was increased, while for a given BIS concentration, the uptake efficiency increased with increasing microgel size in the aggregate. We attribute this to the nature of the aggregates; aggregates have void space between the microgels that can serve as reservoirs for Orange II uptake-the void spaces are hypothesized to increase with larger diameter microgels. By exploiting the thermoresponsive nature of the microgels, and microgel based aggregates, 85.3 % removal efficiencies can be achieved. Finally, all uptake trends for the aggregates, at room temperature, were fit with a Langmuir sorption isotherm model.

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