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        <identifier>oai:www.ideals.illinois.edu:2142/113019</identifier>
        <datestamp>2023-07-11</datestamp>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:contributor>Marinas, Benito J</dc:contributor>
          <dc:contributor>Marinas, Benito J</dc:contributor>
          <dc:contributor>Bellon, Pascal</dc:contributor>
          <dc:contributor>Espinosa-Marzal, Rosa</dc:contributor>
          <dc:contributor>Cusick, Roland</dc:contributor>
          <dc:creator>Mosiman, Daniel S</dc:creator>
          <dc:date>2022-01-12T21:45:38Z</dc:date>
          <dc:date>2022-01-12T21:45:38Z</dc:date>
          <dc:date>2021-07-12</dc:date>
          <dc:date>2021-08</dc:date>
          <dc:description>Fluoride (F-) is one of the most significant inorganic contaminants endemic to groundwaters worldwide. An estimated 200 million people, mostly in rural low-income regions, have or risk incurring fluorosis because they consume water with F- levels above the World Health Organization’s (WHO) recommended level of 1.5 mg/L. Calcium hydroxyapatite (HAP, Ca5(PO4)3X, where X=OH) nanoparticles (NPs) formed into pellets and used in fixed-bed column reactors are among a handful of technologies recommended by the WHO for low income contexts. 
In the environmental engineering discipline, HAP has historically been considered a F- adsorbent, understood as surface-limited uptake by replacement of OH- at surface-terminated X lattice sites. However, this work demonstrates that HAP NPs not only adsorb but also internalize F- into the bulk of its structure under environmentally relevant conditions (i.e. pH=5-9 and [F-]=1.5-30 mg/L) by the migration of F- to subsurface X and defect lattice sites, yielding fluoro-hydroxyapatite solid solutions (FHAP, Ca5(PO4)3X, where X=OH/F). The practical implication is that there is a potential four to ten-fold increase in F- removal capacity with the utilization of bulk sites.
To accomplish this (Chapter 2), an array of experimental techniques were employed to develop a robust particle model to quantify the adsorption and total (i.e. adsorption and bulk) F- capacity specific to the B-type carbonated HAP sample under investigation. Comparison with batch test F- removal revealed uptake far exceeding the adsorption capacity, thereby indirectly validating the occurrence of F- internalization. Rietveld refinement of X-ray diffraction patterns yielded apatite unit cell parameter values a and c. Consistent with the fact that the a parameter of fluorapatite (FAP, Ca5(PO4)3X, where X=F) is significantly smaller than that of HAP, the a parameter of fluoridated HAP samples decreased with increased F- uptake, providing strong physical evidence of F- internalization. Time-resolved quantitative 19F and 1H solid-state Nuclear Magnetic Resonance spectroscopy (NMR) showed the speciation and quantities of removed F- as well as the corresponding losses of HAP OH-, suggesting that a significant portion of F- inserted into conventional and alternative lattice sites occurs without direct replacement of OH-. One dimensional and two dimensional 1H and 1H-19F NMR techniques demonstrated that the removed F- was heterogeneously distributed within the HAP NPs, indicating strong F- concentration gradients are formed at the NP surface with an inwardly migrating boundary.
An attempt was made to directly observe the F- distribution in single fluoridated HAP NPs by utilizing a nascent and powerful microscopy technique, atom probe tomography (APT), at the Australian Centre for Microscopy and Analysis (Chapter 3). 
The particle model framework was used to investigate F- uptake for a number of HAP variants, revealing that F- does not internalize equally or sometimes at all in different types of HAP (Chapter 4). An investigation of their physicochemical properties helped to isolate factors that significantly affect both F- adsorption and internalization. This led to better insights about the potential mechanism of F- internalization as well as ways in which HAP NPs can be synthesized for enhanced performance.</dc:description>
          <dc:description>Submission original under an indefinite embargo labeled 'Open Access'. The submission was exported from vireo on 2022-01-12 without embargo terms</dc:description>
          <dc:description>The student, Daniel Mosiman, accepted the attached license on 2021-07-12 at 10:57.</dc:description>
          <dc:description>The student, Daniel Mosiman, submitted this Dissertation for approval on 2021-07-12 at 11:17.</dc:description>
          <dc:description>This Dissertation was approved for publication on 2021-07-12 at 17:10.</dc:description>
          <dc:description>DSpace SAF Submission Ingestion Package generated from Vireo submission #16860 on 2022-01-12 at 12:44:56</dc:description>
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  Previous issue date: 2021-07-12</dc:description>
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          <dc:identifier>http://hdl.handle.net/2142/113019</dc:identifier>
          <dc:language>en</dc:language>
          <dc:rights>Copyright 2021 Daniel Mosiman</dc:rights>
          <dc:subject>hydroxyapatite</dc:subject>
          <dc:subject>fluoride</dc:subject>
          <dc:subject>water treatment</dc:subject>
          <dc:title>Probing structure-property relationships of calcium hydroxyapatite defluoridation to enhance performance</dc:title>
          <dc:type>text</dc:type>
          <dc:type>Thesis</dc:type>
          <degree>
            <department>Civil &amp; Environmental Eng</department>
            <discipline>Environ Engr in Civil Engr</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
          </degree>
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