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dc.contributor.advisorRohit Karnik and Nicolas G. Hadjiconstantinou.en_US
dc.contributor.authorBoutilier, Michael S. Hen_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Mechanical Engineering.en_US
dc.date.accessioned2017-05-11T19:56:22Z
dc.date.available2017-05-11T19:56:22Z
dc.date.copyright2017en_US
dc.date.issued2017en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/108931
dc.descriptionThesis: Ph. D., Massachusetts Institute of Technology, Department of Mechanical Engineering, 2017.en_US
dc.descriptionPage 230 blank. Cataloged from PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references (pages 221-229).en_US
dc.description.abstractSeparating components of a gas from a mixture is a critical step in several important industrial processes including natural gas purification, hydrogen production, carbon dioxide sequestration, and oxy-combustion. For such applications, gas separation membranes are attractive because they offer relatively low energy costs but can be limited by low flow rates and low selectivities. Nanoporous graphene membranes have the potential to exceed the permeance and selectivity limits of existing gas separation membranes. This is made possible by the atomic thickness of the material, which can support sub-nanometer pores that enable molecular sieving while presenting low resistance to permeate flow. The feasibility of gas separation by graphene nanopores has been demonstrated experimentally on micron-scale areas of graphene. However, scaling up to macroscopic sizes presents significant challenges, including graphene imperfections and control of the selective nanopore size distribution across large areas. The overall objective of this thesis research is to develop macroscopic graphene membranes for gas separation. Investigation reveals that the inherent permeance of large areas of graphene results from the presence of micron-scale tears and nanometer-scale intrinsic defects. Stacking multiple graphene layers is shown to reduce leakage exponentially. A model is developed for the inherent permeance of multi-layer graphene and shown to accurately explain measured flow rates. Applying this model to membranes with created selective pores, it is predicted that by proper choice of the support membrane beneath graphene or adequate leakage sealing, it should be possible to construct a selectively permeable graphene membrane despite the presence of defects. Interfacial polymerization and atomic layer deposition steps during membrane fabrication are shown to effectively seal micron-scale tears and nanometer-scale defects in graphene. The support membrane is designed to isolate intrinsic defects and reduce leakage through tears. Methods of creating a high density of selectively permeable nanopores are explored. Knudsen selectivity is achieved using macroscopic three-layer graphene membranes on polymer supports by high density ion bombardment. Separation ratios exceeding the Knudsen effusion limit are achieved with single-layer graphene on optimized supports by low density ion bombardment followed by oxygen plasma etching, providing evidence of molecular sieving based gas separation through centimeter-scale graphene membranes.en_US
dc.description.statementofresponsibilityby Michael S. H. Boutilier.en_US
dc.format.extent230 pagesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsMIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectMechanical Engineering.en_US
dc.titleDevelopment of macroscopic nanoporous graphene membranes for gas separationen_US
dc.typeThesisen_US
dc.description.degreePh. D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineering
dc.identifier.oclc986241935en_US


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