Publications by authors named "Sotira Yiacoumi"

Solvent-based CO capture consumes significant amounts of energy for solvent regeneration. To improve energy efficiency, this study investigates CO fixation in a solid form through solvation, followed by ionic self-assembly-aided precipitation. Based on the hypothesis that CO ions may bind with monovalent metal ions, we introduced Na into an aqueous hexane-1,6-diamine solution where CO forms carbamate and bicarbonate.

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Accurate prediction of the atmospheric transport of debris particles relies heavily on our knowledge of the size distribution of the particles within a debris cloud. Assuming a fixed particle size during simulations is not always viable since the size distribution of the debris can change during transport. Various microphysical processes, such as aggregation and breakup, influence debris particles and dictate any changes to the size distribution.

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The charging of various airborne particles was investigated using single-particle levitation and charge-balance equations. Though radioactive decay and triboelectrification can induce charging, it is typically assumed that the aerosols in a radioactive plume will not carry significant charge at steady state since atmospheric particles can have their charge neutralized through the capture of adjacent counter-ions (i.e.

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Iodine radioisotopes released during nuclear fuel reprocessing must be removed from the off-gas stream before discharge. One promising material for iodine capture is reduced silver mordenite (AgZ). Nevertheless, the adsorbent's capacity will degrade, or age, over time when the material is exposed to other off-gas constituents.

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Radioactive charging can significantly impact the way radioactive aerosols behave, and as a result their lifetime, but such effects are neglected in predictive model studies of radioactive plumes. The objective of this work is to determine the influence of radioactive charging on the vertical transport of radioactive aerosols in the atmosphere, through its effect on coagulation and deposition, as well as quantifying the impact of this charging on aerosol lifetime. The TwO-Moment Aerosol Sectional (TOMAS) microphysical model was extended to account for radioactive charging effects on coagulation in a computationally efficient way.

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This study focuses on the influence of hydrophilic groups and metal-ion loading on adsorbent polymer conformation, which controls access to adsorption sites and may limit adsorption capacity. Gaining a better understanding of the factors that influence conformation may yield higher-capacity adsorbents. Polyamidoxime (PAO), deuterated-PAO polyacrylic acid diblock copolymers (d-PAO-b-PAA), and randomly configured copolymers (PAO-co-PAA) were synthesized and characterized by neutron reflectometry in air and DO.

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Nuclear power is a relatively carbon-free energy source that has the capacity to be utilized today in an effort to stem the tides of global warming. The growing demand for nuclear energy, however, could put significant strain on our uranium ore resources, and the mining activities utilized to extract that ore can leave behind long-term environmental damage. A potential solution to enhance the supply of uranium fuel is to recover uranium from seawater using amidoximated adsorbent fibers.

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Recovering uranium from seawater has been the subject of many studies for decades, and has recently seen significant progress in materials development since the U.S. Department of Energy (DOE) has become involved.

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Modular chemical process intensification can dramatically improve energy and process efficiencies of chemical processes through enhanced mass and heat transfer, application of external force fields, enhanced driving forces, and combinations of different unit operations, such as reaction and separation, in single-process equipment. These dramatic improvements lead to several benefits such as compactness or small footprint, energy and cost savings, enhanced safety, less waste production, and higher product quality. Because of these benefits, process intensification can play a major role in industrial and manufacturing sectors, including chemical, pulp and paper, energy, critical materials, and water treatment, among others.

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Radioactivity can induce charge accumulation on radioactive particles. However, electrostatic interactions caused by radioactivity are typically neglected in transport modeling of radioactive plumes because it is assumed that ionizing radiation leads to charge neutralization. The assumption that electrostatic interactions caused by radioactivity are negligible is evaluated here by examining charge accumulation and neutralization on particles containing radionuclides in open air.

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Radioactivity can influence surface interactions, but its effects on particle aggregation kinetics have not been included in transport modeling of radioactive particles. In this research, experimental and theoretical studies have been performed to investigate the influence of radioactivity on surface charging and aggregation kinetics of radioactive particles in the atmosphere. Radioactivity-induced charging mechanisms have been investigated at the microscopic level, and heterogeneous surface potential caused by radioactivity is reported.

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Radioactive particles may acquire surface potential through self-charging, and thus can behave differently from natural aerosols in atmospheric systems with respect to aggregation, deposition, resuspension, and transport to areas surrounding a radioactive source. This work focuses on the adhesive force between radioactive particles and metallic surfaces, which relates to the deposition and resuspension of particles on surrounding surfaces. Scanning surface potential microscopy was employed to measure the surface potential of radioactive gold foil.

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Neutron imaging is presented as a tool for quantifying the diffusion of ions inside porous materials, such as carbon electrodes used in the desalination process via capacitive deionization and in electrochemical energy-storage devices. Monolithic mesoporous carbon electrodes of ∼10 nm pore size were synthesized based on a soft-template method. The electrodes were used with an aqueous solution of gadolinium nitrate in an electrochemical flow-through cell designed for neutron imaging studies.

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Neutron reflectometry (NR) was employed to study the interaction of nanosized silica particles with a flat silica surface in aqueous solutions. Unlike other experimental tools that are used to study surface interactions, NR can provide information on the particle density profile in the solution near the interface. Two types of silica particles (25 and 100 nm) were suspended in aqueous solutions of varying ionic strength.

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The kinetic friction force and the adhesion force of Bacillus thuringiensis spores on planar surfaces in atmospheric systems were studied using atomic force microscopy. The influence of relative humidity (RH) on these forces varied for different surface properties including hydrophobicity, roughness, and surface charge. The friction force of the spore was greater on a rougher surface than on mica, which is atomically flat.

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Electrostatic force is investigated as one of the components of the adhesion force between Bacillus thuringiensis (Bt) spores and planar surfaces. The surface potentials of a Bt spore and a mica surface are experimentally obtained using a combined atomic force microscopy (AFM)-scanning surface potential microscopy technique. On the basis of experimental information, the surface charge density of the spores is estimated at 0.

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Adhesion of spores of Bacillus thuringiensis (Bt) and spherical silica particles on surfaces was experimentally and theoretically investigated in this study. Topography analysis via atomic force microscopy (AFM) and electron microscopy indicates that Bt spores are rod shaped, approximately 1.3 mum in length and approximately 0.

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Grand canonical Monte Carlo (GCMC) simulations are employed to study the selective electrosorption of ions from a mixture of symmetric and asymmetric electrolytes confined in pores and results are compared to experimental observations obtained via cyclic voltammetry and batch electrosorption equilibrium experiments. GCMC simulations have the advantage over other Monte Carlo methods to unambiguously quantify the total number of ions in the pore solution. The exclusion parameter and selectivity factor are used to evaluate the selective capacity of pores toward different ionic species under various conditions.

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The size-sieving properties of a mesoporous carbon membrane were studied via molecular permeation and cyclic voltammetry experiments. Two phenomena, simple diffusion and electrochemically aided diffusion, were investigated. Molecular diffusion through the membrane was caused by a concentration gradient across the membrane and was facilitated by electrosorption of ions under an externally applied electric field.

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The formation of the electrical double layer (EDL) in the presence of trivalent and monovalent ions inside a slit-type nanopore was simulated via the canonical Monte Carlo method using a primitive model. In large pores, the distribution of ionic species is similar to that observed in an isolated planar double layer. Screening of surface charge is determined by the competitive effects between ion size and charge asymmetry of the counterions.

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Canonical Monte Carlo simulations of the interaction between a uniformly charged spherical particle and a discretely charged planar surface in solutions of symmetric and asymmetric electrolytes were performed. To assess the nature of the interactions, the force exerted on the colloidal particle perpendicular to the planar surface was calculated. Attractive minima in the interaction force between the similarly charged surfaces reveal the occurrence of two phenomena: long-range attraction of electrostatic origin and short-range attraction due to depletion effects.

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The fundamental mechanism of electrosorption of ions developing a double layer inside nanopores was studied via a combination of experimental and theoretical studies. A novel graphitized-carbon monolithic material has proven to be a good electrical double-layer capacitor that can be applied in the separation of ions from aqueous solutions. An extended electrical double-layer model indicated that the pore size distribution plays a key role in determining the double-layer capacitance in an electrosorption process.

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Electrosorption is generally defined as potential-induced adsorption on the surface of charged electrodes. After polarization of the electrodes, ions are removed from the electrolyte solution by the imposed electric field and adsorbed onto the surface of the electrodes. Experimental and modeling studies were conducted using two types of carbon aerogel composites of different surface areas to provide a better understanding on the mechanisms of electrosorption.

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Unfavorable aggregation and deposition of colloidal particles in natural and engineered systems is still a subject of debate. Complicating factors such as surface roughness, secondary minimum aggregation, and the nature of discrete surface charge and surface potential make it difficult to attribute a specific cause to these phenomena. The presence of surface charge heterogeneity and its influence on interaction forces, which are responsible for aggregation and deposition, are studied in this work through the application of atomic force microscopy (AFM).

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Canonical Monte Carlo (CMC) simulations are employed in this work in order to study the structure of the electrical double layer (EDL) near discretely charged planar surfaces in the presence of symmetric and asymmetric indifferent electrolytes within the framework of a primitive model. The effects of discreteness and strength of surface charge, charge asymmetry, and size asymmetry are specific focuses of this work. The CMC simulation protocol is initially tested against the classical theory, the modified Gouy-Chapman (GC) theory, in order to assess the reliability of the simulation results.

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