(152e) Microfluidic Synthesis of Nano Materials at High Pressures and Temperatures Conference: AIChE Annual MeetingYear: 2009Proceeding: 2009 AIChE Annual MeetingGroup: Catalysis and Reaction Engineering DivisionSession: Invited: Session Honoring Professor James Wei - II Time: Monday, November 9, 2009 - 4:35pm-4:55pm Authors: Jensen, K. F., Massachusetts Institute of Technology Chemically synthesized nano materials such as nanocrystalline quantum dots are being considered as the active element in many applications, including photovoltaics, displays, and bio-chem sensing. In order to realize the promise of these devices, it will be critical to have an efficient, reproducible synthesis technique of the nanostructures. Currently, nanoparticles are synthesized in a batch mode in small volumes, which is appropriate for studying the fundamental properties of nanosized structures and for developing proof of principle device structures. However, batch synthesis suffers from irreproducibility of size, size distribution, and quality of the nano-material from batch to batch. Moreover, there is inherent difficulty in scaling up to quantities more reasonable for device development and optimization. Continuous flow reactors based on microfluidics (microreactors) integrated with heaters and fluid control elements offer a solution to these problems as well as additional advantages. We describe continuous synthesis of nanostructures in microfluidic systems consisting of multiple sub millimiter sized channels in which fluid flows continuously and chemical reactions take place. The small reaction volumes combined with the high heat and mass transfer rates enable reactions to be performed under more aggressive conditions with higher yields than can typically be achieved with conventional reactors. The ability to work at elevated temperatures and pressures while confining potentially toxic, high reactive starting materials is particularly important for the synthesis of novel nanostructured materials.