Temperature responsive hydrogel nanoparticles were created from two hydrophobically modified polymers - poly(N-isopropylacrylamide) copolymerized with N-[4-(1-pyrenyl)butyl]-N-n-octadecylacrylamide] and a cholesterol-bearing microbial polysaccharide called pullulan. Above 32°C, the nanoparticles increased in size but did not aggregate, and resumed their original size when cooled. It was proposed that these nanoparticles could be used as thermal stabilizers for enzymes in biotechnology or as drug carriers.
Temperature responsive hydrogel nanoparticles were created from two hydrophobically modified polymers - poly(N-isopropylacrylamide) copolymerized with N-[4-(1-pyrenyl)butyl]-N-n-octadecylacrylamide] and a cholesterol-bearing microbial polysaccharide called pullulan. Above 32°C, the nanoparticles increased in size but did not aggregate, and resumed their original size when cooled. It was proposed that these nanoparticles could be used as thermal stabilizers for enzymes in biotechnology or as drug carriers.
Temperature responsive hydrogel nanoparticles were created from two hydrophobically modified polymers - poly(N-isopropylacrylamide) copolymerized with N-[4-(1-pyrenyl)butyl]-N-n-octadecylacrylamide] and a cholesterol-bearing microbial polysaccharide called pullulan. Above 32°C, the nanoparticles increased in size but did not aggregate, and resumed their original size when cooled. It was proposed that these nanoparticles could be used as thermal stabilizers for enzymes in biotechnology or as drug carriers.
Temperature responsive hydrogel nanoparticles were created from two hydrophobically modified polymers - poly(N-isopropylacrylamide) copolymerized with N-[4-(1-pyrenyl)butyl]-N-n-octadecylacrylamide] and a cholesterol-bearing microbial polysaccharide called pullulan. Above 32°C, the nanoparticles increased in size but did not aggregate, and resumed their original size when cooled. It was proposed that these nanoparticles could be used as thermal stabilizers for enzymes in biotechnology or as drug carriers.
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Temperature responsive hydrogel nanoparticles have been made by the association of two different
hydrophobically modified polymers in the form of a copolymer of poly(N-isopropylacrylamide) and N-[4-
(1-pyrenyl)butyl]-N-n-octadecylacrylamide] (PNIPAM-C18Py) and one with a cholesterol-bearing microbial polysaccharide, pullulan [65]. Above 32 ◦C, the nanoparticles increased in diameter from 47 to 160 nm, but no aggregation could be detected. On cooling, they resumed their original size. It was speculated that such particles could be used as a thermal stabilizer of enzymes in biotechnology, as well as in drug carrier systems. PEs based on polyacrylonitrile have been prepared from oxidized asphalt [66]. Included are cationic, anionic, and amphoteric varieties, all with hydrophilic acrylic structures. The cationic PEs were made by amination with ethylenediamine and 3-methylaminopropylamine. They exhibited stronger flocculating properties than the amphoteric PEs, and the anionic PEs behaved as stabilisers in dispersed systems of wastewater. It was suggested that the cationic PEs could be used in treating oil refinery and textile wastewaters. 8. Conclusions The enhancement of flotation processes by using PEs has been successfully carried out for a wide range of industrial and domestic wastewaters. The use of flotation processes has the added benefit of a reduced solids load compared to that obtained with inorganic coagulants. Further improvements have been demonstrated with hydrophobically modified cationic PEs in the case of oil and grease removal, and in the treatment of algae/cyanobacteria-laden water. The PE needs to be designed to amalgamate specific contaminants. The challenge now is to apply additives like cationic surfactants, cationic Pes, and especially hydrophobically modified cationic PEs to the cleaning up of intractable wastes, such as those from PFAS-laden waters and microplastics from sewage effluents. Author Contributions: Writing—original draft preparation: B.B.; Writing—review and editing: Z.X. Acknowledgments: This work was supported by CSIRO Manufacturing. Conflicts of Interest: The authors declare no conflict of interest. References 1. Wang, L.K.; Shammas, N.K.; Selke, W.A.; Aulenbach, D.B. (Eds.) Flotation Technology; Springer: Dortrecht, The Netherlands, 2010. 2. Yu, L.; Han, M.; He, F. A review of treating oily wastewater. Arab. J. Chem. 2017, 10, S1913–S1922. [CrossRef] 3. Lee, C.S.; Robinson, J.; Chong, M.F. A review on application of flocculants in wastewater treatment. Process Saf. Environ. Prot. 2014, 92, 489–508. [CrossRef] 4. Bolto, B.A.; Gregory, J. Organic polyelectrolytes in water treatment. Water Res. 2007, 41, 2301–2323. [CrossRef] [PubMed] 5. Bennett, G.F.; Shammus, N.K. Separation of oil from wastewater by air flotation. In Flotation Technology; Wang, L.K., Shammas, N.K., Selke, W.A., Aulenbach, D.B., Eds.; Springer: Dortrecht, The Netherlands, 2010. 6. Bolto, B.A.; Dixon, D.R.; Gray, S.G.; Ha, C.; Harbour, P.J.; Ngoc, L.; Ware, A.J. The application of soluble organic polymers in wastes treatment. Water Sci. Technol. 1996, 34, 117–124. [CrossRef] 7. Hart, J.A. On improving wastewater quality. Water Sew. Works 1970, 117, 20–26. 8. Boyd, J.L.; Shell, G.L.; Dahlstrom, D.A. Treatment of oily wastewaters to meet regulatory standards. AIChE Symp. Ser. 1972, 68, 124. 9. Ellis, M.M.; Fischer, P.W. Clarifying oil field and refinery wastewaters by gas flotation. J. Pet. Technol. 1973, 25, 426–430. [CrossRef] 10. Biesinger, M.G.; Vining, T.S.; Shell, G.L. Industrial experience with dissolved air flotation. In Proceedings of the Purdue University Industrial Waste Conference, Lafeyette, Indiana, 9–10 May 1974; Volume 29, p. 290. 11. Smith, A.W.; Robe, K. Heavy emulsion oil waste reduced from 2000 to 10 ppm. Chem. Process. 1976, 39, 62. 12. Pearson, S.C. Factors influencing oil removal efficiency in dissolved air flotation units. In Proceedings of the 4th Annual Industrial Pollution Conference on WWEMA, Philadelphia, PA, USA, 5–7 June 1976
Catalytic Deoxygenation of Waste Soybean Oil Over Hybrid Catalyst For Production of Bio-Jet Fuel - in Situ Supply of Hydrogen by Aqueous-Phase Reforming (APR) of Glycerol