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- (4bp) Smart Nanotechnology in Biomaterials, Sensors, Actuators and Textiles
In my previous work, smart nano-fibers have been successfully prepared by different methods. For instance, temperature- and pH-dual sensitive hydrogel nano-fibers were prepared by electrospinning technique1,2. The nano-scale size decreased the response time of the smart hydrogel from several hours to a few seconds. In addition, the fibrous mat form provided the hydrogel nano-fibers much easier handling properties than do the conventional hydrogel nano-particles. These hydrogel nano-fibers should be suitable for the applications in sensors/actuators, biomaterials, etc. An alternative to synthesize smart nano-fibers was explored by surface-grafting of nano-fibers with smart polymers3-5. Adsorption of protein on these smart fibers could be actuated by the pH of the environment, e.g., more than 5 times higher adsorption at pHs above 5. These smart nano-fibers have also been demonstrated to be excellent supports for enzyme immobilization as a result of ultra-high specific area. In recent years, smart nano-fibers have also become fast-growing scaffolds for tissue engineering.
My recent work on chemical/biological protective clothing reveals a promising approach to prepare selective and responsive barriers6. This barrier is based on a polymer-polymer nanocomposite of a smart polymer grafted or a smart nano-fiber imbedded within a porous or dense hydrophobic polymer host matrix. The hydrophobic host matrix provides mechanical strength, durability, flexibility, and barrier properties, while the smart polymer/fiber provides high water vapor permeability with stimuli-responsive traits for size-exclusion of toxic chemicals. Preliminary results on poly(ethylene terephthalate) (PET) and poly(methacrylic acid) or poly(2-acrylamido-2-methyl-1-propanesulfonic acid) showed that, selective transport of water vapor over dimethyl methylphosphonate vapor was increased by 12 times for both nanocomposites in comparison to the PET dense membrane.
Reference:
1. Chen, H.; Hsieh, Y.L. Ultra-fine hydrogel fibers with dual temperature and pH sensitivities. Journal of Polymer Science Part A: Polymer Chemistry 2004, 42(24), 6331.
2. Chen, H.; Hsieh, Y.L. Temperature and pH dual-sensitive hydrogels from interpenetrating network (IPN) and copolymerization of N-isopropylacrylamide and sodium acrylate. Journal of Polymer Science Part A: Polymer Chemistry 2004, 42 (13), 3293.
3. Chen, H.; Hsieh, Y.L. Enzyme immobilization on ultra-fine cellulose fibers via poly(acrylic acid) electrolyte grafts. Biotechnology and Bioengineering 2005, 90(4), 405.
4. Hsieh, Y.L.; Wang, Y.H.; Chen, H. Enzyme immobilization onto ultra-high specific surface cellulose fibers via amphiphilic (PEG) spacers and electrolyte (PAA) grafts. ACS Symposium Series: Polymer Biocatalysis and Biomaterials 2005, 900, 63.
5. Hsieh, Y.L.; Xie, J.B.; Wang, Y.H.; Chen, H.; Li, L.; Zhang, L.F.; Cecile, C. Generation of polymer-based nano-porous fibers and protein or enzyme membrane compositions. PCT Int. Appl. (2004), 74 pp. CODEN: PIXXD2 WO 2004044281 A2 20040527.
6. Chen, H.; Palmese, G.R.; Elabd, Y.A. Polyester-polyelectrolyte nanocomposite membranes as breathable and responsive barriers. AIChE Conference, Abstract of Paper, 2005, Cincinnati, OH.