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Description
Within recent years, metal-organic frameworks, or MOF’s, have gained a lot of attention in the materials research community. These micro-porous materials are constructed of a metal oxide core and organic linkers, and have a wide-variety of applications due to their extensive material characteristic possibilities. The focus of this study is

Within recent years, metal-organic frameworks, or MOF’s, have gained a lot of attention in the materials research community. These micro-porous materials are constructed of a metal oxide core and organic linkers, and have a wide-variety of applications due to their extensive material characteristic possibilities. The focus of this study is the MOF-5 material, specifically its chemical stability in air. The MOF-5 material has a large pore size of 8 Å, and aperture sizes of 15 and 12 Å. The pore size, pore functionality, and physically stable structure makes MOF-5 a desirable material. MOF-5 holds applications in gas/liquid separation, catalysis, and gas storage. The main problem with the MOF-5 material, however, is its instability in atmospheric air. This inherent instability is due to the water in air binding to the zinc-oxide core, effectively changing the material and its structure. Because of this material weakness, the MOF-5 material is difficult to be utilized in industrial applications. Through the research efforts proposed by this study, the stability of the MOF-5 powder and membrane were studied. MOF-5 powder and a MOF-5 membrane were synthesized and characterized using XRD analysis. In an attempt to improve the stability of MOF-5 in air, methyl groups were added to the organic linker in order to hinder the interaction of water with the Zn4O core. This was done by replacing the terepthalic acid organic linker with 2,5-dimethyl terephthalic acid in the powder and membrane synthesis steps. The methyl-modified MOF-5 powder was found to be stable after several days of exposure to air while the MOF-5 powder exhibited significant crystalline change. The methyl-modified membrane was found to be unstable when synthesized using the same procedure as the MOF-5 membrane.
ContributorsAnderson, Anthony David (Author) / Lin, Jerry Y.S. (Thesis director) / Ibrahim, Amr (Committee member) / Chemical Engineering Program (Contributor) / Barrett, The Honors College (Contributor)
Created2016-05
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Description
Tri-layer lithium ion battery separators were synthesized by dip-coating macroporous YSZ and mesoporous sol-gel derived gamma-alumina films onto porous polypropylene. These separators were installed into coin-cell lithium ion batteries and subjected to charge/discharge cycle testing to determine specific capacity. The gamma-alumina coated separators exhibited low capacity, while the YSZ coated

Tri-layer lithium ion battery separators were synthesized by dip-coating macroporous YSZ and mesoporous sol-gel derived gamma-alumina films onto porous polypropylene. These separators were installed into coin-cell lithium ion batteries and subjected to charge/discharge cycle testing to determine specific capacity. The gamma-alumina coated separators exhibited low capacity, while the YSZ coated separators failed immediately. Investigation by SEM and a surface wettability test indicated that the gamma alumina and YSZ coatings exhibited low wettability, and the YSZ coating exhibited low porosity. These factors resulted in high internal resistance of the battery, due to electrolyte failing to permeate the separator and provide transport of lithium ions between the electrodes.
ContributorsMcafee, Paul Milton (Author) / Lin, Jerry Y.S. (Thesis director) / Kasik, Alexandra (Committee member) / Barrett, The Honors College (Contributor) / Chemical Engineering Program (Contributor)
Created2015-05
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Description
The United States and most of the world is pushing to significantly reduce carbon emissions, with many countries intent on fostering carbon negative energy processes to offset ozone depletion and climate changes. 30% of the U.S. greenhouse gas emissions are generated from the combustion of fossil fuels to generate electricity1.

The United States and most of the world is pushing to significantly reduce carbon emissions, with many countries intent on fostering carbon negative energy processes to offset ozone depletion and climate changes. 30% of the U.S. greenhouse gas emissions are generated from the combustion of fossil fuels to generate electricity1. Current commercial IGCC carbon capture processes employ a capital and operating cost intensive water-gas shift reaction facilitated by a high temperature reactor followed by a low temperature reactor and an amine absorber to separate the hydrogen and carbon dioxide streams to capture the carbon. Dr. Jerry Y.S. and his laboratory at Arizona State have developed a hydrogen permselective MFI type ZSM-5 zeolite membrane reactor that effectively facilities the water gas shift reaction with high conversion and separates the CO2 and H2 streams during reaction to generate ultrapure retentate and permeate streams. The membrane, formed by secondary free growth, is synthesized on an ultrapure a-alumina membrane support currently purchased from an outside vendor. The purpose of this study was to design an α-alumina support processing plant with capability to supply one full-scale commercial reactor annually with membranes. The design yielded a DCFRoR of 71% for a 20-year project life. A zeolite membrane processing material balance was conducted using alumina support as the raw material. The study showed very low material costs and consumption rates for all materials except a gas used to refine the membrane after processing. The results of both studies were favorable enough to suggest further study.
ContributorsNorman, Taylor Cristine (Author) / Lin, Jerry Y.S. (Thesis director) / Meng, Lie (Committee member) / Chemical Engineering Program (Contributor) / Barrett, The Honors College (Contributor)
Created2017-05