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Salinity Mitigation for Potash Mine Sites: Synergistic Cation and Anion Removal Using a Dual-Adsorbent

dc.contributor.advisorChang, Wonjae
dc.contributor.committeeMemberBarbour, Lee
dc.contributor.committeeMemberLindsay, Matt
dc.contributor.committeeMemberSoltan, Jafar
dc.creatorGibb, Nicholas P 1992-
dc.creator.orcid0000-0003-0156-9197
dc.date.accessioned2017-01-12T22:24:20Z
dc.date.available2018-10-16T17:31:19Z
dc.date.created2016-12
dc.date.issued2017-01-12
dc.date.submittedDecember 2016
dc.date.updated2017-01-12T22:24:20Z
dc.description.abstractPotash (KCl) mining generates large quantities of tailings and brine which can impact proximate aquifers, elevating the concentrations of Na+, K+, and Cl-. To desalinate brine-impacted groundwater near potash mines and other inland locations, two adsorbents were sequentially applied: (1) calcined layered double hydroxide (CLDH), to adsorb anions, divalent cations, and transiently raise the pH; and (2) acid-treated clinoptilolite zeolite, to adsorb monovalent cations and neutralize the effluent pH. To evaluate this dual-adsorbent process, equilibrium adsorption experiments were conducted and the adsorbents were characterized through X-ray diffraction, X-ray florescence, porosimetry, scanning electron microscopy, and synchrotron-based scanning transmission X-ray microscopy. Using synthetic NaCl solution, the Langmuir maximum adsorption capacity for Cl- onto CLDH and Na+ onto acid-treated zeolite was 116.3 and 28.4 mg/g, respectively. The Na+ uptake was greatly enhanced by solution pre-treatment (dechlorination) using CLDH, and also by zeolite acid treatment (with 1M = 2 M > 0.1 M > untreated, irrespective of acid type). Pre-conditioning the zeolite with Na+ prior to acid treatment also improved the adsorption capacity and promoted crystallinity. Desalination of potash brine-impacted groundwater was systematically investigated. Under the optimal conditions, the dual-adsorbent reduced the concentration of Cl- by 95.8%, Ca2+ by 89.8%, Mg2+ by 92.3%, Na+ by 91.9%, K+ by 96.5%, preserved a neutral pH (7.72), and lowered the sodium adsorption ratio (36.5 to 12.5) and the hardness (574 to 56.3 mg/L as CaCO3). In contrast, natural zeolite alone only removed 51.2% of the Na+ and 79.6% of the K+, and also generated extremely hard water (3620 mg/L as CaCO3) due to Ca2+ and Mg2+ exchange. Finally, zeolite regeneration studies were conducted using 0.1 M HCl. The Na+ was efficiently desorbed, but K+ remained. Over four consecutive adsorption–desorption cycles, the net K+ loading increased from 4.8 to 21.2 mg/g. This K-form zeolite could potentially be applied as a slow-release fertilizer, thereby transforming a potash mining waste material into a valuable resource.
dc.format.mimetypeapplication/pdf
dc.identifier.urihttp://hdl.handle.net/10388/7686
dc.subjectZeolite
dc.subjectLayered double hydroxide
dc.subjectDesalination
dc.subjectSodium adsorption
dc.subjectPotassium adsorption
dc.subjectChloride adsorption
dc.subjectRegeneration
dc.titleSalinity Mitigation for Potash Mine Sites: Synergistic Cation and Anion Removal Using a Dual-Adsorbent
dc.typeThesis
dc.type.materialtext
local.embargo.terms2018-01-12
thesis.degree.departmentCivil and Geological Engineering
thesis.degree.disciplineEnvironmental Engineering
thesis.degree.grantorUniversity of Saskatchewan
thesis.degree.levelMasters
thesis.degree.nameMaster of Science (M.Sc.)

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