Publications by authors named "Leila Dehabadi"

The aim of this study was to develop a facile and novel lipid-based formulation of vitamin C and vitamin D3. Liposomes loaded with vitamin C and D3 were characterized using transmission electron microscopy (TEM) and zeta potential measurements for evaluating morphology, particle size and physical stability. HPLC was employed to quantify the content of vitamin C and vitamin D3 in their liposomal forms.

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The adsorption-desorption behavior of flax fibers (FFs) is reported in this paper. FFs are a potential desiccant material for air-to-air energy wheels, which transfer heat and moisture in building heating, ventilation, and air conditioning (HVAC) systems. The raw FFs sample was subjected to physical modification, followed by complementary material characterization to understand the relationship between its structure and its moisture uptake performance.

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The role of chemical modification of pristine linen fiber (LF) on its physicochemical and adsorption properties is reported in this contribution. The surface and textural properties of the pristine LF and its peroxyacetic acid- (PAF) and chlorite-treated (CF) fiber forms were characterized by several complementary methods: spectroscopy (SEM, TEM, FT-IR, and XPS), thermal analysis (DSC and TGA), gas/water adsorption isotherms, and zeta potential (ξ). The results obtained reveal that the surface charge and textural properties (surface area and pore structure) of the LF material was modified upon chemical treatment, as indicated by changes in the biomass composition, morphology, ξ-values, and water/dye uptake properties of the fiber samples.

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The physicochemical and hydration properties of mechanically modified flax fibers (FFs) were investigated herein. Raw flax fibers (FF-R) were ball-milled and sieved through mesh with various aperture sizes (420, 210, and 125 μm) to achieve modified samples, denoted as FF-420, FF-210, and FF-125, respectively. The physicochemical and hydration properties of FF-R with variable particle sizes were characterized using several complementary techniques: microscopy (SEM), spectroscopy (FT-IR, XRD, and XPS), thermoanalytical methods (DSC and TGA), adsorption isotherms using gas/dye probes, and solvent swelling studies in liquid HO.

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This study reports on the adsorption (dehumidification)-desorption (humidification) behavior of cetylpyridinium bromide (CPB) coated starch particles (SPs), denoted as SP-CPB, as a potential desiccant material for air-to-air energy exchangers. CPB is a cationic surfactant with antibacterial activity that can be used to modify the surface properties of SPs, especially at variable CPB loading levels (SP-CPB0.5, SP-CPB2.

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Molecular selective adsorption processes at the solid surface of biopolymers in mixed solvent systems are poorly understood due to manifold interactions. However, the ability to achieve adsorptive fractionation of liquid mixtures is posited to relate to the role of specific solid-liquid interactions at the adsorbent interface. The hydration of solid biopolymers (amylose, amylopectin, cellulose) in binary aqueous systems is partly governed by the relative solvent binding affinities with the biopolymer surface sites, in accordance with the role of textural and surface chemical properties.

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This study reports on the unique water vapor adsorption properties of biomass-derived starch particles (SPs). SPs offer an alternative desiccant for air-to-air energy exchangers in heating, ventilation, and air conditioning systems because of their remarkable adsorption-desorption performance. SP has a particle diameter ( ) of 15 μm with a surface area (SA) of 2.

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Polysaccharides (PS) of cellulose, soluble, corn- and maize-derived starches with variable amylose/amylopectin content were cross-linked with epichlorohydrin (EPI) to form polymeric adsorbents. The properties of the cross-linked PS-EPI materials were prepared by varying the synthesis conditions (nature of polysaccharide, temperature, and reagent ratios) to afford network polymer materials with tunable properties. The optimized polymers were obtained at a reaction temperature (50-54 °C) according their yield were characterized using spectroscopic (IR and NMR) methods, and thermal gravimetric analysis (TGA).

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