Abstract
The creation of geometrically complex fluidic devices is a subject of broad fundamental and technological interest. Here, we demonstrate the fabrication of three-dimensional (3D) microvascular networks through direct-write assembly of a fugitive organic ink. This approach yields a pervasive network of smooth cylindrical channels (∼10–300 μm) with defined connectivity. Square-spiral towers, isolated within this vascular network, promote fluid mixing through chaotic advection. These vertical towers give rise to dramatic improvements in mixing relative to simple straight (1D) and square-wave (2D) channels while significantly reducing the device planar footprint. We envisage that 3D microvascular networks will provide an enabling platform for a wide array of fluidic-based applications.
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01 April 2003
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Notes
* An error has led to the arrows in Fig. 3b being doubled. This has been corrected in the full text version and will be corrected in an erratum in the May issue of Nature Materials, from which there will be a link to the original paper.
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Acknowledgements
This work has been sponsored by the AFOSR Aerospace and Materials Science Directorate (Grant no. F49620-00-1-0094) and the National Science Foundation (Grant no. DMI 00-99360 and DMR-01-177792). Electron microscopy was carried out in the Center for Microanalysis of Materials, University of Illinois, which is supported by the US Department of Energy. Support for D. Therriault came from the University of Illinois through a CARVER Fellowship and a Nanoscience and Technology Center Fellowship, and the government of Québec (NATEQ). The robotic deposition apparatus used in this work was designed and built by J. Cesarano, and customized software for 3D fabrication was developed by J.E. Smay. The authors gratefully acknowledge the thoughtful comments and technical advice of colleagues R. Adrian, H. Aref, J. Moore, N. Sottos and P. Wiltzius.
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Therriault, D., White, S. & Lewis, J. Chaotic mixing in three-dimensional microvascular networks fabricated by direct-write assembly. Nature Mater 2, 265–271 (2003). https://doi.org/10.1038/nmat863
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DOI: https://doi.org/10.1038/nmat863