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- All Subjects: Membranes
- All Subjects: MOF
- Creators: Anderson, Anthony David
- Creators: Arafa, Omar M.
- Member of: Barrett, The Honors College Thesis/Creative Project Collection
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 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
Description
This report investigates the mass-transfer kinetics of gas diffusion through an asymmetrical hollow-fiber membrane developed for the membrane biofilm reactor (MBfR) when it is used to microbiologically convert syngas (a mixture of H2, CO2, and CO) to organic products. The asymmetric Matrimid® membrane had superior diffusion fluxes compared to commercially available symmetric, three-layer composite and polypropylene single-layer membranes. The Matrimid® asymmetric membrane had a H2 gas-gas diffusion flux between 960- and 1600-fold greater than that of the composite membrane and between 32,000- and 46,800-fold greater than that of the single-layer membrane. Gas-gas diffusion experiments across the Matrimid® membrane also demonstrated plasticization behavior for pure CO2 and H2 gas feeds. In particular, a 10 psia increase in inlet pressure resulted in a 12-fold increase in permeance for H2 and a 16-fold increase for CO2. Plasticization was minimal for symmetric composite and single-layer membranes. Thus, diffusion fluxes were much higher for the asymmetric membrane than for the symmetric composite and single-layer membranes, and this supports the promise of the asymmetric membrane as a high-efficiency means to deliver syngas to biofilms able to convert the syngas to organic products. Gas-liquid diffusion was much slower than gas-gas diffusion, and this supports the benefit of using the MBfR approach over fermentation reactors that rely on sparging syngas.
ContributorsArafa, Omar M. (Author) / Rittmann, Bruce (Thesis director) / Torres, Cesar (Committee member) / Chemical Engineering Program (Contributor) / W.P. Carey School of Business (Contributor) / Barrett, The Honors College (Contributor)
Created2018-05