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Description
A wireless hybrid device for detecting volatile organic compounds (VOCs) has been developed. The device combines a highly selective and sensitive tuning-fork based detector with a pre-concentrator and a separation column. The selectivity and sensitivity of the tuning-fork based detector is optimized for discrimination and quantification of benzene, toluene, ethylbenzene,

A wireless hybrid device for detecting volatile organic compounds (VOCs) has been developed. The device combines a highly selective and sensitive tuning-fork based detector with a pre-concentrator and a separation column. The selectivity and sensitivity of the tuning-fork based detector is optimized for discrimination and quantification of benzene, toluene, ethylbenzene, and xylenes (BTEX) via a homemade molecular imprinted polymer, and a specific detection and control circuit. The device is a wireless, portable, battery-powered, and cell-phone operated device. The device has been calibrated and validated in the laboratory and using selected ion flow tube mass spectrometry (SFIT-MS). The capability and robustness are also demonstrated in some field tests. It provides rapid and reliable detection of BTEX in real samples, including challenging high concentrations of interferents, and it is suitable for occupational, environmental health and epidemiological applications.
ContributorsChen, Zheng (Author) / Tao, Nongjian (Thesis advisor) / Chae, Junseok (Committee member) / Forzani, Erica (Committee member) / Arizona State University (Publisher)
Created2011
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Description
Volatile Organic Compounds (VOCs) are central to atmospheric chemistry and have significant impacts on the environment. The reaction of oxygenated VOCs with OH radicals was first studied to understand the fate of oxygenated VOCs. The rate constants of the gas-phase reaction of OH radicals with trans-2-hexenal, trans-2-octenal, and trans-2 nonenal

Volatile Organic Compounds (VOCs) are central to atmospheric chemistry and have significant impacts on the environment. The reaction of oxygenated VOCs with OH radicals was first studied to understand the fate of oxygenated VOCs. The rate constants of the gas-phase reaction of OH radicals with trans-2-hexenal, trans-2-octenal, and trans-2 nonenal were determined using the relative rate technique. Then the interactions between VOCs and ionic liquid surfaces were studied. The goal was to find a material to selectively detect alcohol compounds. Computational chemistry calculations were performed to investigate the interactions of ionic liquids with different classes of VOCs. The thermodynamic data suggest that 1-butyl-3-methylimindazolium chloride (C4mimCl) preferentially interacts with alcohols as compared to other classes of VOCs. Fourier transform infrared spectroscopy was used to probe the ionic liquid surface before and after exposure to the VOCs that were tested. New spectral features were detected after exposure of C4mimCl to various alcohols and a VOC mixture with an alcohol in it. The new features are characteristic of the alcohols tested. No new IR features were detected after exposure of the C4mimCl to the aldehyde, ketone, alkane, alkene, alkyne or aromatic compounds. The experimental results demonstrated that C4mimCl is selective to alcohols, even in complex mixtures. The kinetic study of the association and dissociation of alcohols with C4minCl surfaces was performed. The findings in this work provide information for future gas-phase alcohol sensor design. CO2 is a major contributor to global warming. An ionic liquid functionalized reduced graphite oxide (IL-RGO)/ TiO2 nanocomposite was synthesized and used to reduce CO2 to a hydrocarbon in the presence of H2O vapor. The SEM image revealed that IL-RGO/TiO2 contained separated reduced graphite oxide flakes with TiO2 nanoparticles. Diffuse Reflectance Infrared Fourier Transform Spectroscopy was used to study the conversion of CO2 and H2O vapor over the IL-RGO/TiO2 catalyst. Under UV-Vis irradiation, CH4 was found to form after just 40 seconds of irradiation. The concentration of CH4 continuously increased under longer irradiation time. This research is particularly important since it seems to suggest the direct, selective formation of CH4 as opposed to CO.
ContributorsGao, Tingting (Author) / Andino, Jean M (Thesis advisor) / Forzani, Erica (Committee member) / Kavazanjian, Edward (Committee member) / Arizona State University (Publisher)
Created2012
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Description
Cardiovascular disease is affecting millions of people worldwide and is the leading cause of death in the United States. This disease is closely related to the abnormal creatinine levels in blood. For this reason, there is a need for a low-cost point-of-care device that could measure the creatinine level in

Cardiovascular disease is affecting millions of people worldwide and is the leading cause of death in the United States. This disease is closely related to the abnormal creatinine levels in blood. For this reason, there is a need for a low-cost point-of-care device that could measure the creatinine level in blood with the goal of managing and preventing cardiovascular disease. This project introduces a Molecular Reactive Lateral Flow Assay (MoReLFA) device that is aimed toward creatinine detection based on an optimized chemical reaction of creatinine and alkaline picrate. The device consists of different membranes that accommodate 50 microliters of fluid sample and carry out a colorimetric reaction, in which deposited-colored region is analyzed for Red, Green, and Blue (RGB) components via an image processing software. The color intensity from the RGB outputs was then studied and compared with a gold standard spectrophotometry-based technique. The results show that the MoReLFA sensor could successfully detect creatinine levels in standard solutions. The plot of the sensor color intensity against the absorbance from spectrophotometry shows a good correlation between the two methods (R2 = 0.96). Furthermore, the paper introduces the development of a RGB reader box that is portable and for easy assessment of RGB values. The color intensity from the box shows an increasing trend with increasing creatinine concentrations; and the coefficient of determination of this relationship is 0.85.
ContributorsNguyen, Ngan Anh (Author) / Raupp, Gregory (Thesis advisor) / Forzani, Erica (Thesis advisor) / Mora, Sabrina Jimena (Committee member) / Arizona State University (Publisher)
Created2022