Nanomagnetit-bentonit vizes közegű diszperz rendszereinek zeta-potenciáljának vizsgálata

The stability of different type nanomaterials play an important role among recent scientific and industrial challenges, including the examination of the effect of polymers, surfactants and their mixture on surface and electric surface properties and aggregation extent of dispersed particles, which are of utmost importance. Bentonite and its composite with different nanomaterials are frequently used for instance in environmental protection for wastewater treatment, since due to their great specific surface area they have excellent sorption properties. There are several publications in the literature for the application of bentonite in drilling muds. By using them the fluid loss can be decreased during the drilling process, the filtration of the fluid can be increased, it also improves the rheological properties and the formation damage can also be mitigated. During research the investigation and the analysis of the zeta-potential of nanoparticles and their composites at different pH and salt content can be an interesting topic. During our experiments the electric surface properties of nanomagnetite synthetized in laboratory (NM), cation exchanged bentonite from Mád (Be) and the composite particles of these particles were investigated. Hybrid particles of different compositions (9:1, 7:3, 1:1, 3:7, 1:9) were analyzed at different potassium chloride concentrations (0.1 – 0.0001 M). The surface adsorption on the surface, i.e. the change in the surface charge can be traced well by analyzing the obtained zeta-potential values. The behavior of such systems was observed in the full pH interval, thus, valuable data were obtained regarding the colloidal stability. As for the stability, different requirements may emerge in practice, there are application fields where the colloidally stable system is advantageous, on the other hand, in some cases, ceasing the stabile system is the goal. Our investigations are of high importance in terms of stability and its characterization [1].

Hybrid Perovskite/Polymer Materials: Preparation and Physicochemical Properties

The aim of this work is to investigate the preparation, the optical properties, and the stability over time of a colloidal organic–inorganic hybrid perovskite (CH3NH3PbBr3)/random copolymer P(MMA-co- DMAEMA) system. Different ratios of perovskite to copolymer were used to study its effect on stability and properties. The optical properties were investigated by UV-Vis and fluorescence spectroscopy. Dynamic light scattering was used to determine the size, and the size polydispersity of the colloidal hybrid particles; while morphology was investigated by transmission electron microscopy. Photoluminescence decay studies revealed the interaction of the random copolymer with the perovskite. Finally, thin-films were prepared, to investigate the optical properties of the samples in the absence of the solvent. High temporal stability of the optical properties of thin hybrid films was observed under certain conditions.

Robust ZnO/HNTs-Based Superhydrophobic Cotton Fabrics With UV Shielding, Self-Cleaning, Photocatalysis, and Oil/Water Separation

In this work, robust superhydrophobic cotton fabrics with UV shielding, self-cleaning, photocatalysis, and oil/water separation were successfully prepared based on micro/nano hierarchical ZnO/HNTs (halloysite nanotubes) hybrid particles and silicone elastomer polydimethylsiloxane (PDMS). ZnO/HNTs hybrid particles were prepared by in-situ growth of ZnO nanoparticles on the surface of halloysite nanotubes (HNTs). ZnO/HNTs hybrid particles and PDMS were used to successively coat cotton fabric by dip-coating approach. The coated cotton fabric displayed excellent superhydrophobicity with a water contact angle of 162.5 ± 1° and photocatalytic degradation of methylene blue solution under UV irradiation owing to the roughness and photocatalytic performance provided by micro/nano hierarchical ZnO/HNTs hybrid particles and low surface energy achieved by PDMS. The as-prepared fabric also displayed outstanding self-cleaning and antifouling properties. In addition, due to its both superhydrophobic and superoleophilic characteristics, the as-prepared cotton fabric can be used to separate several oil/water mixtures and showed good recoverability. The superhydrophobic cotton fabric also exhibited excellent UV shielding performance with a large UV protection factor of 1643.28 due to strong ultraviolet-absorption, light scattering and frequent light reflection of ZnO nanoparticles in ZnO/HNTs composites coated on cotton fabric. Importantly, the as-prepared fabric retained superhydrophobic performance after 2000 cycles rubbing, 90h UV illumination, and immersing in acidic and alkali solutions with different pH values ranging from 1 to 14 for 1 h. These characteristics make multifunctional cotton fabrics a satisfactory candidate in various promising fields.

Mesoporous Poly(melamine-co-formaldehyde) Particles for Efficient and Selective Phosphate and Sulfate Removal

Due to the existence-threatening risk to aquatic life and entire ecosystems, the removal of oxyanions such as sulfate and phosphate from anthropogenic wastewaters, such as municipal effluents and acid mine drainage, is inevitable. Furthermore, phosphorus is an indispensable resource for worldwide plant fertilization, which cannot be replaced by any other substance. This raises phosphate to one of the most important mineral resources worldwide. Thus, efficient recovery of phosphate is essential for ecosystems and the economy. To face the harsh acidic conditions, such as for acid mine drainage, an adsorber material with a high chemical resistivity is beneficial. Poly(melamine-co-formaldehyde) (PMF) sustains these conditions whilst its very high amount of nitrogen functionalities (up to 53.7 wt.%) act as efficient adsorption sides. To increase adsorption capacities, PMF was synthesized in the form of mesoporous particles using a hard-templating approach yielding specific surface areas up to 409 m2/g. Different amounts of silica nanospheres were utilized as template and evaluated for the adsorption of sulfate and phosphate ions. The adsorption isotherms were validated by the Langmuir model. Due to their properties, the PMF particles possessed outperforming maximum adsorption capacities of 341 and 251 mg/g for phosphate and sulfate, respectively. Furthermore, selective adsorption of sulfate from mixed solutions of phosphate and sulfate was found for silica/PMF hybrid particles.

Effects of Sub-Micro Sized BaTiO3 Blocking Particles and Ag-Deposited Nano-Sized BaTiO3 Hybrid Particles on Dielectric Properties of Poly(vinylidene-fluoride) Polymer

This work provided an alternative route to balance the significantly increased dielectric permittivity (ε′) and effectively retained tanδ using an effective two-step concept. Ag-deposited nano-sized BaTiO3 (Ag-nBT) hybrid particle was used as the first filler to increase the ε′ of the poly(vinylidene-fluoride) (PVDF) polymer via the strong interfacial polarization and a high permittivity of nBT and suppress the increased loss tangent (tanδ) owing to the discrete growth of Ag nanoparticles on the surface of nBT, preventing a continuous percolating path. The ε′ and tanδ values at 103 Hz of the Ag-nBT/PVDF composite with fAg-nBT~0.29 were 61.7 and 0.036. The sub-micron-sized BaTiO3 (μBT) particle was selected as the blocking particles to doubly reduce the tanδ with simultaneously enhanced ε′ due to the presence of the tetragonal BT phase. The μBT blocking particles can effectively further inhibit the formation of conducting network and hence further reducing tanδ. By incorporation of μBT clocking particles with fμBT = 0.2, the ε′ value of the Ag-nBT/PVDF-μBT composite (fAg-nBT = 0.30) can significantly increase to 161.4, while the tanδ was reduced to 0.026. Furthermore, the tanδ was lower than 0.09 in the temperature range of −60–150 °C due to the blocking effect of μBT particles.

Silica-Supported Styrene-Co-Divinylbenzene Pickering Emulsion Polymerization: Tuning Surface Charge and Hydrophobicity by pH and Co-Aid Adsorption

In this work, polymerizations of styrene (St) in the presence of divinylbenzene (DVB) as a crosslinking agent and sodium 4-vinylbenzenesulfonate (VBS) have been performed in Pickering emulsions, using silica nanoparticles (SNps) as stabilizing agents and ammonium persulfate as a hydrophilic initiator. In oil-in-water Pickering emulsions with alkaline continuous phase (pH = 9) at 1, 2, and 3 wt% DVB (relative to St), polydisperse spheroid copolymer submicronic nanoparticles were obtained. Comparatively, polymerizations performed in Pickering emulsions with acidic continuous phase (pH = 5) allowed preparing St-co-DVB microspheres with core–shell structures at 1 wt% DVB and St-co-DVB hybrid monoliths with bi-continuous morphologies at 2 and 3 wt% DVB. It is noteworthy that this work reports Pickering emulsion polymerization as a new strategy for preparing hybrid percolated scaffolds with bi-continuous porosity. The proposed mechanisms originated by pH, DVB, and VBS and the drastic impact caused on the final morphology obtained, either hybrid particles or monoliths, are discussed herein.