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All Subjects: Ion Exchange
Resource Type: Text

Future H2O: Front-end Design Experience

Description

As we already know, fresh water is essential to human life as it sustains and replenishes our bodies. Water sustainability is clearly an important issue that need to be addressed in our world of growing demand and shrinking resources. The ASU Future H2O program seeks to make a difference in the development of water sustainability programs by performing experiments that convert urine into reusable water. The goal is to make reusable water processes become inexpensive and easily accessible to local businesses. This promises a significant environmental impact. In order to make the process of development more efficient we can combine engineering technology with scientific experimentation. As an engineering student and an advocate of water sustainability, I have a chance to design the front-end platform that will use IoT to make the experimental process more accessible and effective. In this paper, I will document the entire process involved in the designing process and what I have learned.

ContributorsTran, Phung Thien (Author) / Boscovic, Dragan (Thesis director) / Boyer, Treavor (Committee member) / School of Earth and Space Exploration (Contributor) / Computer Science and Engineering Program (Contributor) / Barrett, The Honors College (Contributor)

Created2018-05

Enzyme-Induced Carbonate Precipitation Utilizing Fresh Urine and Calcium-Rich Zeolites

Description

Enzyme-induced carbonate precipitation (EICP) is a biocementation technique that produces comparatively fewer carbon dioxide emissions than traditional cementation. However, the use of synthetic reagents for EICP is costly, and the process produces an ammonium byproduct which is a harmful pollutant. This study utilizes fresh urine as a source of urea and calcium-rich zeolites as an ammonium adsorbent and a source of calcium ions for the EICP cementation technique. Batch hydrolysis and adsorption experiments were conducted to determine the effects of zeolite type, zeolite form, and solution composition on ammonium adsorption and calcium release. Cementation experiments were then conducted to determine the effects of different hydrolysis and adsorption times on ammonium adsorption and calcium carbonate precipitation. The results showed that calcium-rich chabazite could be used as a source of calcium ions and as an effective adsorbent of ammonium for EICP. Additionally, synthetic, fresh urine and real, fresh urine had comparable ammonium adsorption and calcium release trends. Finally, inclusion of a pre-hydrolysis step reduced the ammonium adsorption and calcium release, but longer adsorption times lead to calcium carbonate precipitation outside of the sand column, which is an undesirable outcome for soil biocementation; even with this limitation, the calcium carbonate content of sand columns ranged from 0.48% to 0.92%, which signifies the potential of the proposed process for cementation, given a higher initial concentration of urea.

ContributorsCrane, Lucas Christopher (Author) / Boyer, Treavor (Thesis director) / Hamdan, Nasser (Committee member) / Civil, Environmental and Sustainable Eng Program (Contributor) / School of Sustainable Engineering & Built Envirnmt (Contributor) / Barrett, The Honors College (Contributor)

Created2021-05

Effect of anion exchange resin properties on the adsorption of PFAAs and NOM

Description

Humans are exposed up to thousands of per- and polyfluoroalkyl substances (PFAS) in the environment, but most of the research and action has been directed towards only two PFAS compounds. These two compounds are part of a subcategory of PFAS called perfluoroalkyl acids (PFAAs). It has been a challenge for the environmental community to mitigate risks caused by PFAAs due to their high persistence and lack of effective measures to remove them from the environment, especially in heavily impacted areas like fire-training sites. The goal of this work was to further answer some questions regarding the removal of PFAAs in the environment by looking at anion exchange resin characteristics and presence of a competing compound, natural organic matter (NOM), in the adsorption of environmentally relevant PFAS compounds including the two often monitored 8-carbon chain PFAAs. Two different resins were tested with two forms of counterions, in both groundwater and NOM impacted groundwater. Resin polymer matrix was the most important property in the adsorption of PFAAs, the two resins used A520E and A860 had similar properties except for their matrices polystyrene (PS) and polyacrylic (PA), respectively. The PS base is most effective at PFAAs adsorption, while the PA is most effective at NOM adsorption. The change in the counterion did not negatively affect the adsorption of PFAAs and is, therefore, a viable alternative for future studies that include regeneration and destruction of PFAAs. The presence of NOM also did not significantly affect the adsorption of PFAAs in the PS resin A520E, although for some PFAAs compounds it did affect adsorption for the PA resin. Ultimately, PS macroporous resins with a strong Type I or Type II base work best in PFAAs removal.

Contributorsdel Moral, Lerys Laura (Author) / Boyer, Treavor (Thesis advisor) / Abbaszadegan, Morteza (Committee member) / Hamilton, Kerry (Committee member) / Arizona State University (Publisher)

Created2019