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Characterization of micromanipulator-controlled dry spinning of micro- and sub-microscale polymer fibers

Scott M Berry et al 2006 J. Micromech. Microeng. 16 1825-1832   doi: 10.1088/0960-1317/16/9/010  Help

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Scott M Berry1,2, Steven A Harfenist2,4, Robert W Cohn2 and Robert S Keynton1,2,3
1 Department of Mechanical Engineering, University of Louisville, Louisville, KY 40292, USA
2 ElectroOptics Research Institute and Nanotechnology Center, University of Louisville, Louisville, KY 40292, USA
3 Department of Bioengineering, University of Louisville, 437 Lutz Hall, Louisville, KY 40292, USA
4 Current address: Department of Physics, California Polytechnic State University, San Luis Obispo, CA 93407, USA

Abstract. No current microfabrication technique exists for producing room- temperature, high-precision, point-to-point polymer micro- and sub- microscale fibers in three dimensions. The purpose of this work is to characterize a novel method for fabricating interconnected three- dimensional (3-D) structures of micron and sub-micron feature size. Poly- (methyl methacrylate) (PMMA) micro- and sub-microscale fiber suspended bridges are fabricated at room temperature by drawing from pools of solvated polymer using a nano-tipped stylus that is precisely positioned by an ultra-high-precision micromilling machine. The fibers were drawn over a 1.8 mm silicon trench, and as the solvent in the solution bridge rapidly evaporates, a suspended, 3-D PMMA fiber remained between the two pools. The resulting fiber diameters were measured for solutions of PMMA in chlorobenzene with concentrations ranging from 15.5 to 23.0 wt% 495k g mol−1 PMMA and 13.0 to 21.0 wt% 950k g mol−1 PMMA. Fibers were found to increase in diameter from 450 nm to 50 µm, roughly corresponding to the increase in concentration of PMMA. To minimize fiber diameter variance, different stylus materials were investigated, with a Parylene®-coated stylus producing fibers with the lowest variance in diameter. Overall, the fiber diameter was found to increase significantly as the solution concentration and polymer molecular weight increased.

Print publication: Issue 9 (September 2006)
Received 17 March 2006, in final form 30 June 2006
Published 28 July 2006

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