Energy and Mineral Resources for a Sustainable Future

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https://hdl.handle.net/10388/14354

As Saskatchewan and the world transition from fossil-fuel-based energy systems, innovative solutions are needed to meet energy needs in a sustainable manner that goes hand-in-hand with public policy development to ensure all communities receive equal access to affordable and secure energy sources.

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Stabilization of Oil-in-Water Pickering Emulsions by Surface-Functionalized Cellulose Hydrogel
(Gels, 2024-10) Udoetok, Inimfon; Mohamed, Mohamed H.; Wilson, Lee
An amphiphilic cellulose (CLH) hydrogel was synthesized via grafting of quaternary ammonium groups onto cellulose. The structural properties of CLH were characterized via Fourier transform infrared (FTIR)/13C solid-state NMR spectroscopy, elemental (CHN) analysis, particle size distribution (PSD), thermogravimetric analysis (TGA), and wettability was assessed through contact angle measurements. Pickering emulsions of apolar oils in water were prepared using variable weights of the CLH hydrogel as the stabilizing agent, along with different methods of agitation (mechanical shaking and sonication). The characterization results for CLH provide support for the successful grafting of quaternary ammonium groups onto cellulose to produce hydrogels. Different methods of agitation of an oil/water mixture revealed the formation of an oil-in-water (O/W) Pickering emulsion that was stable to coalescence for over 14 days. The resulting emulsions showed variable droplet sizes and stability according to the dosage of CLH in the emulsion and the agitation method, where the emulsion droplet size is related to the particle size of CLH. The addition of methyl orange (MO), a probe to evaluate the phase partitioning of the dye, had minor effects on the emulsion droplet size, and the emulsion prepared with 0.8 wt.% of CLH and agitated via sonication exhibited the smallest droplet size and greatest stability. This study is anticipated to catalyze further research and the development of low-cost and sustainable biopolymer hydrogels as stabilizers for tunable Pickering emulsion. Grafted cellulose materials of this type represent versatile stabilizing agents for foods, agrochemicals, and pharmaceutical products and technologies.
Hybrid Chitosan Biosorbents: Tunable Adsorption at Surface and Micropore Domains
(Biomimetics, 2024-11) Udoetok, Inimfon; Mohamed, Mohamed H.; Wilson, Lee
Herein, we report a study that provides new insight on the knowledge gaps that relate to the role of biopolymer structure and adsorption properties for chitosan adsorbents that are cross-linked with glutaraldehyde. The systematic modification of chitosan cross-linked with glutaraldehyde (CG) and its quaternized forms (QCG) was studied in relation to the reaction conditions: mole ratios of reactants and pH conditions. Complementary adsorbent characterization employed 13C NMR/FTIR spectroscopy, TGA and DSC, point-zero-charge (PZC), solvent swelling, and sorption studies using selected dye probes. The spectral and thermal techniques provide complementary evidence that affirm the key role of cross-linker content and quaternization on variation of the physicochemical properties of chitosan. The PZC results reveal a neutral surface charge for the modified materials between pH 6.0 to 6.3 ± 0.3, as compared with pH 8.7 ± 0.4 for pristine chitosan. Solvent swelling in water decreased with greater cross-linking, while the QCG materials had greater swelling over CG materials due to enhanced hydration. The adsorption results reveal variable dye uptake properties according to the cross-linker content. Similarly, surface versus micropore adsorption was demonstrated, according to the nature and ionization state of the dye for the modified adsorbents, where the CG and QCG materials had tunable sorption properties that exceeded that of unmodified chitosan. A key step in tuning the structure and surface chemical properties of cross-linked chitosan involves pH control during synthesis. The facile tunability of the physicochemical properties of the modified biopolymers reported herein means that they possess features of biomimetics that are relevant to advanced drug delivery, antimicrobial materials for wound healing, biosensors, and biosorbents for biomedical applications.
Low adsorption affinity of athabasca oil sands naphthenic acid fraction compounds to a peat-mineral mixture
(Elsevier, 2024-04-24) Meulen, Ian J. Vander; Steiger, Bernd G.K.; Asadi, Mohsen; Peru, Kerry M.; Degenhardt, Dani; McMartin, Dena W.; McPhedran, Kerry M.; Wilson, Lee D.; Headley, John V.
Much of the toxicity in oil sands process-affected water in Athabasca oil sands tailings has been attributed to naphthenic acids (NAs) and associated naphthenic acid fraction compounds (NAFCs). Previous work has characterized the environmental behaviour and fate of these compounds, particularly in the context of constructed treatment wetlands. There is evidence that wetlands can attenuate NAFCs in natural and engineered contexts, but relative contributions of chemical, biotic, and physical adsorption with sequestration require deconvolution. In this work, the objective was to evaluate the extent to which prospective wetland substrate material may adsorb NAFCs using a peat-mineral mix (PMM) sourced from the Athabasca Oil Sands Region (AOSR). The PMM and NAFCs were first mixed and then equilibrated across a range of NAFC concentrations (5–500 mg/L) with moderate ionic strength and hardness (∼200 ppm combined Ca2+ and Mg2+) that approximate wetland water chemistry. Under these experimental conditions, low sorption of NAFCs to PMM was observed, where sorbed concentrations of NAFCs were approximately zero mg/kg at equilibrium. When NAFCs and PMM were mixed and equilibrated together at environmentally relevant concentrations, formula diversity increased more than could be explained by combining constituent spectra. The TOC present in this PMM was largely cellulose-derived, with low levels of thermally recalcitrant carbon (e.g., lignin, black carbon). The apparent enhancement of the concentration and diversity of components in PMM/NAFCs mixtures are likely related to aqueous solubility of some PMM-derived organic materials, as post-hoc combination of dissolved components from PMM and NAFCs cannot replicate enhanced complexity observed when the two components are agitated and equilibrated together.

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