Electrolyte-induced aggregation of zein protein nanoparticles in aqueous dispersions.

Ion specific effects on the charging and aggregation features of zein nanoparticles (ZNP) were studied in aqueous suspensions by electrophoretic and time-resolved dynamic light scattering techniques. The influence of mono- and multivalent counterions on the colloidal stability was investigated for positively and negatively charged particles at pH values below and above the isoelectric point, respectively. The sequence of the destabilization power of monovalent salts followed the prediction of the indirect Hofmeister series for positively charged particles, while the direct Hofmeister series for negatively charged ones assumed a hydrophobic character for their surface.

Colloidal Interactions of Microplastic Particles with Anionic Clays in Electrolyte Solutions.

Homoaggregation of polystyrene microplastics (MPs) and heteroaggregation of MPs with anionic clay minerals, namely, layered double hydroxide (LDH), in different salt (NaCl, CaCl, and NaSO) solutions were systematically investigated using light scattering techniques. The salt type and ionic strength had significant effects on the stability of both MPs and LDH particles individually and the results could be explained by DLVO theory and the Schulze-Hardy rule. However, once stable colloidal dispersions of the individual particles were mixed, heteroaggregation occurred between the oppositely charged MPs and LDH, which was also confirmed by transmission electron microscopy and X-ray scattering.

The Influence of Solvents and Colloidal Particles on the Efficiency of Molecular Antioxidants.

The radical scavenging activity of three molecular antioxidants (trolox, rutin and ellagic acid) was investigated in different solvents with and without added polymer-based colloidal particles (SL-IP-2). Rutin and ellagic acid showed poor solubility in water, preventing the accurate measurement of the effective antioxidant concentration values, which were determined in ethanol/water (EtOH/HO) mixtures. The presence of trolox and rutin changed neither the surface charge properties nor the size of SL-IP-2 in these solvents, while significant adsorption on SL-IP-2 was observed for ellagic acid leading to overcharging and rapid particle aggregation at appropriately high antioxidant concentrations in EtOH/HO.

Delamination of Layered Double Hydroxide in Ionic Liquids under Ambient Conditions.

Liquid phase delamination of layered materials into single- or few-layer nanosheets leads to stable nanoscale dispersions of 2D materials. The delamination of layered double hydroxide (LDH) to double hydroxide nanosheets was studied in two ionic liquids (ILs): ethylammonium nitrate (EAN) and 1-butyl-3-methylimidazolium thiocyanate (BMIMSCN). The as-prepared lamellar structure of LDH disappeared upon dispersing it in ILs due to delamination into 2D nanosheets confirmed by X-ray scattering and diffraction techniques and further evaluated by height profile assessment of the nanoparticles by atomic force microscopy.

Structure-Stability Relationship in Aqueous Colloids of Latex Particles and Gemini Surfactants.

The influence of gemini surfactants (GSs) on the charging and aggregation features of anionic sulfate modified latex (SL) particles was investigated by light scattering techniques in aqueous dispersions. The GSs of short alkyl chains (2-4-2 and 4-4-4) resembled simple inert salts and aggregated the particles by charge screening. The adsorption of GSs of longer alkyl chains (8-4-8, 12-4-12, and 12-6-12) on SL led to charge neutralization and overcharging of the particles, giving rise to destabilization and restabilization of the dispersions, respectively.

Antioxidant colloids via heteroaggregation of cerium oxide nanoparticles and latex beads.

Antioxidant colloids were developed via controlled heteroaggregation of cerium oxide nanoparticles (CeO NPs) and sulfate-functionalized polystyrene latex (SL) beads. Positively charged CeO NPs were directly immobilized onto SL particles of opposite surface charge via electrostatic attraction (SL/Ce composite), while negatively charged CeO NPs were initially functionalized with poly(diallyldimethylammonium chloride) (PDADMAC) polyelectrolyte and then, aggregated with the SL particles (SPCe composite). The PDADMAC served to induce a charge reversal on CeO NPs, while the SL support prevented nanoparticle aggregation under conditions, where the dispersions of bare CeO NPs were unstable.

Aggregation of Halloysite Nanotubes in the Presence of Multivalent Ions and Ionic Liquids.

Colloidal stability was investigated in two types of particle systems, namely, with bare (h-HNT) and polyimidazolium-functionalized (h-HNT-IP-2) alkali-treated halloysite nanotubes in solutions of metal salts and ionic liquids (ILs). The valence of the metal ions and the number of carbon atoms in the hydrocarbon chain of the IL cations (1-methylimidazolium (MIM), 1-ethyl-3-methylimidazolium (EMIM), 1-butyl-3-methylimidazolium (BMIM), and 1-hexyl-3-methylimidazolium (HMIM)) were altered in the measurements. For the bare h-HNT with a negative surface charge, multivalent counterions destabilized the dispersions at low values of critical coagulation concentration (CCC) in line with the Schulze-Hardy rule.

Design of hybrid biocatalysts by controlled heteroaggregation of manganese oxide and sulfate latex particles to combat reactive oxygen species.

The preparation of an antioxidant hybrid material by controlled heteroaggregation of manganese oxide nanoparticles (MnO2 NPs) and sulfate-functionalized polystyrene latex (SL) beads was accomplished. Negatively charged MnO2 NPs were prepared by precipitation and initially functionalized with poly(diallyldimethylammonium chloride) (PDADMAC) polyelectrolyte to induce charge reversal allowing decoration of oppositely charged SL surfaces via simple mixing. The PDADMAC-functionalized MnO2 NPs (PMn) aggregated with the SL particles leading to the formation of negatively charged, neutral and positively charged (SPMn) composites.

Specific Ion Effects on Aggregation and Charging Properties of Boron Nitride Nanospheres.

The charging and aggregation properties of boron nitride nanospheres (BNNSs) were investigated in the presence of electrolytes of different compositions and valences in aqueous suspensions. The influence of mono- and multivalent cations (counterions) and anions (coions) on the colloidal stability of the negatively charged particles was studied over a wide range of salt concentrations. For monovalent ions, similar trends were determined in the stability and charging of the particles irrespective of the salt composition, i.

Masking specific effects of ionic liquid constituents at the solid-liquid interface by surface functionalization.

Ion specific effects of ionic liquid (IL) constituents on the surface charge and aggregation properties of two types of particles (positively charged amidine (AL) and polyimidazolium-functionalized sulfate (SL-IP-2) latexes) were investigated in IL solutions containing different anions and the 1-butyl-3-methylimidazolium cation. For the AL systems, the affinity of IL anions to the particle surface followed the sequence chloride < bromide < nitrate < acetate. The critical coagulation concentration values decreased in the same order indicating that ion specific adsorption determines the surface charge density and the extent of the repulsive interparticle forces.

Ion Specific Effects on the Stability of Halloysite Nanotube Colloids-Inorganic Salts versus Ionic Liquids.

Charging and aggregation processes were studied in aqueous dispersions of halloysite nanotubes (HNTs) in the presence of monovalent inorganic electrolytes and ionic liquid (IL) constituents. The same type of co-ion (same sign of charge as HNT) was used in all systems, while the type of counterions (opposite sign of charge as HNT) was systematically varied. The affinity of the inorganic cations to the HNT surface influenced their destabilizing power leading to an increase in the critical coagulation concentration (CCC) of HNT dispersions in the Cs < K < Na order.

Magnetic-Field-Manipulated Growth of Flow-Driven Precipitate Membrane Tubes.

Chemobrionics is an emerging scientific field focusing on the coupling of chemical reactions and different forms of motion, that is, transport processes. Numerous phenomena appearing in various gradient fields, for example, pH, concentration, temperature, and so on, are thoroughly investigated to mimic living systems in which spatial separation plays a major role in proper functioning. In this context, chemical garden experiments have received increased attention because they inherently involve membrane formation and various transport processes.