2021
DOI: 10.1016/j.colsurfa.2021.127333
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TiO2 nanoparticle dispersions in water and nonaqueous solvents studied by gravitational sedimentation analysis: Complementarity of Hansen Parameters and DLVO interpretations

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Cited by 25 publications
(5 citation statements)
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“…The local reaction depends on a series of factors inherent to the local pH of the internal environment or the surface charge of the nanoparticles, the positively charged ones being more toxic since they enter cells more quickly than the negative and neutral ones [238]. In this sense, it is essential to keep in mind the difference in the ionic solubility of the different compounds, which change according to the dispersion media properties being different between aqueous and organic solvents [239]. There are other parameters to consider regarding the solubility of inorganic nanoparticles, which tends to increase in acidic solutions, such as gastric fluids [201].…”
Section: Physical Chemical Propertiesmentioning
confidence: 99%
“…The local reaction depends on a series of factors inherent to the local pH of the internal environment or the surface charge of the nanoparticles, the positively charged ones being more toxic since they enter cells more quickly than the negative and neutral ones [238]. In this sense, it is essential to keep in mind the difference in the ionic solubility of the different compounds, which change according to the dispersion media properties being different between aqueous and organic solvents [239]. There are other parameters to consider regarding the solubility of inorganic nanoparticles, which tends to increase in acidic solutions, such as gastric fluids [201].…”
Section: Physical Chemical Propertiesmentioning
confidence: 99%
“…203 However, both DLVO theory and ζ-potential analysis are most reliable in aqueous solutions or in polar organic solvents with high dielectric constants; in more nonpolar organic solvents, other forces such as solute−solvent interactions have a larger effect. 207 Additionally, NCs suspended in nonpolar organic solvents are often terminated by long chain ligands; for these samples, steric repulsion by these large organic ligands may have greater contribution than electrostatic repulsion toward preventing NC aggregation. Nevertheless, if the NC surface charge is postsynthetically modified via surface reduction/ oxidation or ligand exchange, it is likely that these electrostatic changes may have a non-negligible effect upon colloidal stability.…”
Section: Effects Of Surface Electrostaticsmentioning
confidence: 99%
“…Ligand-exchanged CdSe NCs have been shown to be colloidally stable when |ζ-potential| > 30 mV . However, both DLVO theory and ζ-potential analysis are most reliable in aqueous solutions or in polar organic solvents with high dielectric constants; in more nonpolar organic solvents, other forces such as solute–solvent interactions have a larger effect . Additionally, NCs suspended in nonpolar organic solvents are often terminated by long chain ligands; for these samples, steric repulsion by these large organic ligands may have greater contribution than electrostatic repulsion toward preventing NC aggregation.…”
Section: Nc Surface Electrostaticsmentioning
confidence: 99%
“…The results seen in Figure 4 showed that destabilization of HAp, HAp@Cal, and HAp@Cal@5-flu dispersion occurs due to sedimentation. This is evidenced by an increase in the clarity of the suspension in the upper layer with increasing time tests [77][78][79]. To analyze the destabilization kinetics of the obtained dispersions, the Turbiscan Stability Index (TSI) (Turbiscan-specific parameter) was used, which allows us to compare several systems to each other.…”
Section: Turbiscan Analysismentioning
confidence: 99%