Journal articles on the topic 'Binary Nanoparticle Suspensions'

A novel micro/nanoscale rough structured superhydrophilic hybrid-coated mesh that shows underwater superoleophobic behavior is fabricated by spray casting or dipping nanoparticle–polymer suspensions on stainless steel mesh substrates. Water droplets can spread over the mesh completely; meanwhile, oil droplets can roll off the mesh at low tilt angles without any penetration. Besides overcoming the oil-fouling problem of many superhydrophilic coatings, this superhydrophilic and underwater superoleophobic mesh can be used to separate oil and water. The simple method used here to prepare the organic–inorganic hybrid coatings successfully produced controllable micro-nano binary roughness and also achieved a rough topography of micro-nano binary structure by controlling the content of inorganic particles. The mechanism of oil–water separation by the superhydrophilic and superoleophobic membrane is rationalized by considering capillary mechanics. Tetraethyl orathosilicate (TEOS) as a base was used to prepare the nano-SiO2 solution as a nano-dopant through a sol-gel process, while polyvinyl alcohol (PVA) was used as the film binder and glutaraldehyde as the cross-linking agent; the mixture was dip-coated on the surface of 300-mesh stainless steel mesh to form superhydrophilic and underwater superoleophobic film. Properties of nano-SiO2 represented by infrared spectroscopy and surface topography of the film observed under scanning electron microscope (SEM) indicated that the film surface had a coarse micro–nano binary structure; the effect of nano-SiO2 doping amount on the film’s surface topography and the effect of such surface topography on hydrophilicity of the film were studied; contact angle of water on such surface was tested as 0° by the surface contact angle tester and spread quickly; the underwater contact angle to oil was 158°, showing superhydrophilic and underwater superoleophobic properties. The effect of the dosing amount of cross-linking agent to the waterproof swelling property and the permeate flux of the film were studied; the oil–water separation effect of the film to oil–water suspension and oil–water emulsion was studied too, and in both cases the separation efficiency reached 99%, which finally reduced the oil content to be lower than 50 mg/L. The effect of filtration times to permeate flux was studied, and it was found that the more hydrophilic the film was, the stronger the stain resistance would be, and the permeate flux would gradually decrease along with the increase of filtration times.

A sessile droplet comprising of a nanoparticle aqueous suspension in a binary solution exhibits interesting dissolution dynamics, which may be explored for the formation of toroidal or spherical nanocolloidal assemblies with highly ordered particle arrangement.

Cu2ZnSnS4(CZTS) is a promising semiconductor material for photovoltaic applications,with excellent optical and electronic properties while boasting a nontoxic, inexpensive, andabundant elemental composition. Previous high‐quality CZTS thin films often required eithervacuum‐based deposition processes or the use of organic ligands/solvents for ink formulation,which are associated with various issues regarding performance or economic feasibility. To addressthese issues, an alternative method for depositing CZTS thin films using an aqueous‐basednanoparticle suspension is demonstrated in this work. Nanoparticles of constituent binary sulfides(CuxS and ZnS) are stabilized in an ink using tin(IV)‐based, metal chalcogenide complexes such as[Sn2S6]4‐. This research paper provides a systematic study of the nanoparticle synthesis and inkformulation via the enabling role of the tin chalcogenide complexing power, the deposition of highqualityCZTS thin films via spin coating and annealing under sulfur vapor atmosphere, theirstructural characterization in terms of nanocrystal phase, morphology, microstructure, anddensification, and their resultant optoelectronic properties.

In this study, water is apprehended as conventional fluid with the suspension of two types of hybrid nanoparticles, namely, single-walled CNTs (SWCNTs) and multiwalled CNTs (MWCNTs). The influence of a magnetic field, thermal radiation, and activation energy with binary chemical reaction has been added to better examine the fine point of hybrid nanofluid flow. The mathematical structure regarding the physical model for hybrid nanofluid is established and then the similarity variables are induced to transmute the leading PDEs into nonlinear ODEs. These equations were solved using the shooting technique together with RKF 4-5th order for various values of the governing parameters numerically. The results of prominent parameters were manifested through graphs and tables. The results indicate that the hybrid nanofluid SWCNT − MWCNT / water is fully adequate in cooling and heating compared to other hybrid nanofluids. In addition, the rise in the value of activation energy E upsurges the nanoparticle transfer rate of hybrid nanofluid.

Cefixime; widely employed cephalosporin antibiotic is unfortunately coupled to poor water solubility with resultant low oral bioavailability issues. To solve this problem micro-emulsion technique was used to fabricate binary SLNs using blend of solid and liquid lipids, surfactant as well as co-surfactant. The optimized nano suspension was characterized followed by modification to solidified dosage form. During characterization, optimized nano-suspension (CFX-4) produced particle size 189±2.1 nm with PDI 0.310±0.02 as well as −33.9±2 mV zeta potential. Scanning electron microscopy (SEM) presented nearly identical and spherical shaped particles. Differential scanning calorimetry and X-ray powder diffraction analysis ascertained decrease in drug’s crystallinity. In-vitro release of drug pursued zero-order characteristics and demonstrated non-fickian pattern of diffusion. The freeze dried nano suspension (CFX-4) was transformed to capsule dosage form to perform comparison based In-Vivo studies. In-Vivo evaluation corresponded to 2.20-fold and 2.11-fold enhancement in relative bioavailability of CFX nano-formulation (CFX-4) as well as the prepared capsules respectively in contrast to the commercialized product (Cefiget®). In general; the obtained results substantiated superior oral bioavailability along with sustained pattern of drug release for CFX loaded binary nano particles. Thus, binary SLNs could be employed as a resourceful drug carrier for oral CFX delivery.

The PRHD@MnFe2O4 binary hybrids have shown a potential for applications in the biomedical field. The polymer cover/shell provides sufficient surface protection of magnetic nanoparticles against adverse effects on the biological systems, e.g., it protects against Fenton’s reactions and the generation of highly toxic radicals. The heating ability of the PRHD@MnFe2O4 was measured as a laser optical density (LOD) dependence either for powders as well as nanohybrid dispersions. Dry hybrids exposed to the action of NIR radiation (808 nm) can effectively convert energy into heat that led to the enormous temperature increase ΔT 170 °C (>190 °C). High concentrated colloidal suspensions (5 mg/mL) can generate ΔT of 42 °C (65 °C). Further optimization of the nanohybrids amount and laser parameters provides the possibility of temperature control within a biologically relevant range. Biological interactions of PRHD@MnFe2O4 hybrids were tested using three specific cell lines: macrophages (RAW 264.7), osteosarcoma cells line (UMR-106), and stromal progenitor cells of adipose tissue (ASCs). It was shown that the cell response was strongly dependent on hybrid concentration. Antimicrobial activity of the proposed composites against Escherichia coli and Staphylococcus aureus was confirmed, showing potential in the exploitation of the fabricated materials in this field.

Global agricultural systems are under unprecedented pressures due to climate change. Advanced nano-engineering can help increase crop yields while ensuring sustainability. Nanotechnology improves agricultural productivity by boosting input efficiency and reducing waste. Alkaloids as one of the numerous secondary metabolites that serve variety of cellular functions essential for physiological processes. This study tests the competence of silver nanoparticles (AgNPs) in boosting alkaloids accumulation in Catharanthus roseus suspension cultures in relation to the expression of C. roseus Mitogen Activated Protein Kinase 3 (CrMPK3) and Strictosidine Synthase (STR) genes. Five concentrations (5, 10, 15, 20 and 25 mg·L−1) of AgNPs were utilized in addition to deionized water as control. Results reflected binary positive correlations among AgNPs concentration, oxidative stress indicated with increase in hydrogen peroxide and malondialdehyde contents, activities of ascorbate peroxidase and superoxide dismutase, expression of the regulatory gene CrMPK3 and the alkaloid biosynthetic gene STR as well as alkaloids accumulation. These correlations add to the growing evidence that AgNPs can trigger the accumulation of alkaloids in plant cells through a signaling pathway that involves hydrogen peroxide and MAPKs, leading to up-regulation of the biosynthetic genes, including STR gene.

, Page no - | ABSTRACT | PDF | FULL TEXT | e-PUB Background: The development of innovative eco-sustainable bio-nano-composites materials based on cellulose nanomaterials obtained from agricultural waste such as rapeseed plant straw and polymeric materials with improved properties. At first, cellulose was extracted from rapeseed plant straw and cellulosic and no cellulosic materials were estimated. It was found that the rapeseed plant straw contained about 43.48 wt.% cellulosic materials and 56.52 wt.% no cellulosic materials. It was also found that the rapeseed plant straw content about 34.84 wt.% α- cellulose. Then, nano-cellulose was prepared by acid hydrolysis of α -cellulose obtained from rapeseed plant straw. Poly vinyl acetate (PVAc) was prepared by soap free emulsion polymerization of vinyl monomer. Natural rubber (NR) collected as latex was oxidized by KMnO4. Blends of NR and oxidized NR with PVAc of different compositions such as NR60/PVAc40, NR40/PVAc60, ONR60/PVAc40, ONR40/PVAc60 were prepared by mixing NR latex and PVAc emulsion and followed by drying in an oven at 60°C. Composites of NR60/PVAc40 and ONR60/PVAc40 reinforced nano-cellulose (NC) were also prepared in similar way. The blends and composites were then characterized by FTIR, SEM, and Tensile test (TS). FTIR analysis confirmed the oxidation of NR and shown the variation of the functional groups in the blends and composites compared with the FTIR spectrum of NR, ONR and PVAc. SEM study exhibited that the nano-cellulose were dispersed within NR/PVAc and ONR/PVAc blends matrices with a little agglomeration. The tensile test results showed that the strength in composites was increased due to the reinforcing effect of nano-cellulose (NC). Objectives: The aim of this study is to assess the Preparation and characterization of binary blends of NR and oxidized NR with PVAc. Methods: This is an observational study. The study used to be carried out in the admitted patient’s Department of Applied Chemistry and Chemical Engineering, Islamic University, Kushtia-7003, Bangladesh. The duration of the period from Data was entered in MS Excel and Statistical analysis was done using SPSS trial version. Results: This study shows that the according to Constituent, Cellulose was 43.4822%, Alpha-Cellulose were 34.8427% and Cellulose were 8.6395%. And according to Source, Rice Straw were 32.15% %, Sugarcane were 41-43%, Rye Straw were 31.8-42.64%, Corn Stalks were 29.80% and Wheat Straw were 34-40%. Conclusion: Novel eco-friendly bio-nano-composites substances primarily based on renewable and sustainable assets namely natural rubber (NR) and nano-cellulose received from rapeseed plant straw as properly as poly vinyl acetate (PVAc) have been developed. In order to enhance the interfacial interactions amongst the composite factors such as NR, PVAc and NC, oxidation of the NR latex was once carried out by way of KMnO4 before blending mixing with PVAc emulsion and NC suspension.

The automotive design process and the materials in the automotive industry in recent years has caused great interest to the industrial and academic sector. In this study was to evaluate the effect of the amount of bentonite on the thermal and rheological properties of the compound bentonite / paraffin wax. Two bentonite ratios were used: paraffin wax (40:60 and 30:70). The paraffin was characterized by Fourier transform infrared spectroscopy (FTIR), the bentonite was characterized by means of x-ray diffraction (XRD), thermogravimetric analysis (TGA), X-ray fluorescence (XRF). The bentonite/paraffine wax composite was characterized by differential-scanning calorimetry (DSC) and rheology. The sample that contains a higher amount of bentonite shows a lower latent heat, and this could cause a greater heat transfer. Finally, the sample that has a lower amount of bentonite evidenced a lower viscosity, and it could be related to a lower interaction between the particles. 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AbstractMultispeckle x-ray photon correlation spectroscopy measurements, carried out at beamline 8-ID at the Advanced Photon Source at Argonne National Laboratory, of opaque suspensions of silica nanoparticles in water and lutidine-water binary mixtures are presented.

AbstractCurrent binary nanofluid synthesis methods with heat transfer additives lack an understanding of the chemistry of the nanoparticle-additive-base fluid interaction, which plays a significant role in the adsorption of the surfactant on the nanoparticle surface. Consequently, this leads to the formation of aggregates within the nanofluid after a couple of days, affecting the stability of the colloidal suspension. Here, a lithium bromide-alumina salt-based nanofluid is proposed following a newly developed synthesis method including particle surface functionalisation. The new procedure developed allows the initial preparation of the nanoparticles with the surfactant as the first step (surface functionalisation) and then the preparation of the base fluid with a dispersion stabilising agent (Gum Arabic) separately. This is then followed by the dispersion of the prepared alumina nanoparticles into the base fluid, by stirring and ultrasonication to produce the final nanofluid, lithium bromide-water (LiBr-H2O)-alumina nanofluid. Until now, proper procedures have not been reported for the nanofluid synthesis combining surfactant and dispersant and the chemistry of nanoparticles-surfactant-base fluid interaction, which was thoroughly investigated in the new approach. The fluid prepared by both the conventional and new procedures was characterised and analysed simultaneously. A thermal conductivity enhancement of 3% was achieved by using the surface functionalisation method, with greater particle concentration distribution (number of particles in suspension) of 22.7% over the conventional procedure. It also achieved a 5% decrease in dynamic viscosity. On the other hand, a Mouromtseff number value between 0.7 and 1.8 was obtained for the fluid at 293 K and 373 K temperature range, indicating a strong heat transfer capability. It was apparent from the particle size and concentration distribution analysis conducted that this procedure produced a more stable nanofluid with a high distribution of nanoparticles within the fluid. This allows high improvement of thermal properties of the fluid. Graphical abstract Graphical abstract of a new procedure for nanofluid synthesis with heat transfer additives using the two-step method

One of the greatest challenges in the manufacturing and development of nanotechnologies is the requirement for robust, reliable, and accurate characterization data. Presented here are the results of an interlaboratory comparison (ILC) brought about through multiple rounds of engagement with NanoSight Malvern and ten pan-European research facilities. Following refinement of the nanoparticle tracking analysis (NTA) technique, the size and concentration characterization of nanoparticles in liquid suspension was proven to be robust and reproducible for multiple sample types in monomodal, binary, or multimodal mixtures. The limits of measurement were shown to exceed the 30–600 nm range (with all system models), with percentage coefficients of variation (% CV) being calculated as sub 5% for monodisperse samples. Particle size distributions were also improved through the incorporation of the finite track length adjustment (FTLA) algorithm, which most noticeably acts to improve the resolution of multimodal sample mixtures. The addition of a software correction to account for variations between instruments also dramatically increased the accuracy and reproducibility of concentration measurements. When combined, the advances brought about during the interlaboratory comparisons allow for the simultaneous determination of accurate and precise nanoparticle sizing and concentration data in one measurement.

AbstractIn this study, Superparamagnetic magnetite nanoparticles (SPMNPs) are used in a new way as direct nanocarrier for Doxorubicin hydrochloride (DOX) via the functionalization of their surface with tri-sodium citrate through ligand exchange to conjugate DOX with imine bond to form tri-sodium citrate functionalized magnetite loaded DOX nanoparticles (DOX/Cit-MNPs). The DOX/Cit-MNPs were coated with chitosan to form chitosan coated citrate functionalized magnetite loaded DOX nanoparticles (Cs/DOX/Cit-MNPs) to offer biodegradability and pH-sensitive drug release features. The Fourier transform infrared spectroscopy (FTIR) analysis confirmed functionalization of SPMNPs, DOX-conjugation, and chitosan coating. The trans electron microscopy (TEM) show spherical nanostructures with average size 40 nm for coated nanocarriers. The saturation magnetization value of carrier was 59 emu/g.The in-vitro release of DOX from the chitosan coated tri-sodium citrate functionalized magnetite loaded DOX nanoparticles (Cs/DOX/Cit-MNPs) was studied to be 75% at pH 5.5 and 28.6% at pH 7.4 which proves the pH sensitivity of encapsulated Cs/DOX/Cit-MNPs. The effect of Cs/DOX/Cit-MNPs toward Human Breast Cancer Cell lines (MCF7) was studied and found to be 76% without magnet and 98% with external magnet after 72 h. With increasing DOX concentration and treatment time, the cell inhibition (IR%) of DOX solution and Cs/DOX-Cit-MNPs suspension to all cells is increased. Cs/DOX/Cit-MNPs showed sustained release and good inhibition to cancer cells and offer a protective mode for normal cells (WISH) compared to the free DOX. Graphical Abstract

Structural correlations between colloids in a binary mixture of charged and neutral spheres are calculated using computer simulations of the primitive model with explicit microions. For aqueous suspensions in a solvent of large dielectric constant, the traditional Derjaguin-Landau-Vervey-Overbeek (DLVO) theory of linear screening, supplemented with hard core interactions, reproduces the structural correlations obtained in the full primitive model quantitatively. However for lower dielectric contrast, the increasing Coulomb coupling between the counterions and charged colloids results in strong deviations. We find a fluid-fluid phase separation into two regions either rich in charged or rich in neutral colloids which is not reproduced by DLVO theory. Our results are verifiable in scattering or real-space experiments on charged-neutral mixtures of colloids or nanoparticles.

Introduction: Apart from the targeted production of many metal and oxide nanomaterials with desired properties (so- called engineered nanoparticles) and their wide and diverse use in engineering, science, and medicine, even more important potential health risks to human health may be associated with some old technologies. Non-engineered metal oxide nanoparticles (MeO-NPs) generated spontaneously during arc welding, production of steel and non-ferrous metals, pollute the workplace and ambient air along with submicron particles (> 100 nm) of the same metal oxides. The most important sources of by-production of zinc oxide nanoparticles include primary smelting or re-smelting of brass, an alloy of copper and zinc of various proportions (sometimes with a much lower amount of lead, tin, and other metals). The rationale of the study of the comparative and combined toxicity of zinc oxide nanoparticles (ZnO-NPs) and copper oxide nanoparticles (CuO-NPs) is their simultaneous presence in aerosol emissions from brass metallurgy. The objective of our study was to estimate the comparative and combined toxicity of ZnO-NPs and CuO-NPs. Methods: Stable suspensions of MeO-NPs obtained by laser ablation of 99.99 % pure zinc and copper under a layer of deionized water, were injected intraperitoneally 18 times during 6 weeks to outbred male rats separately (in equal mass doses) or in combination for a comparative assessment and analysis of the type of the combined exposure to the studied nanoparticles for a large number of signs (including DNA fragmentation). Results: We established that, judging by some direct and indirect evidence, the subchronic effect of ZnO-NPs on the body was more detrimental than that of CuO-NPs. The mathematical description of the results using the response surface method showed that, similar to other previously studied binary toxic combinations, the response of the body to the combined exposure to CuO and ZnO nanoparticles was characterized by a complex interaction of various types of combined toxicity, depending on the effect it was evaluated for, the levels of the effect and doses. When analyzing the type of the combined effect of ZnO-NPs and CuO-NPs, we observed both the antagonism and additivity according to some indicators of the state of the body, which makes us evaluate their combined exposure as dangerous.

Abstract We report the synthesis of Ag/bentonite, ZnO/bentonite and Ag/ZnO/bentonite nanocomposites (NCs) using Hagenia abyssinica plant extract and their antibacterial study. The synthesized NCs were characterized by using many advanced techniques. The X-ray diffraction and high resolution transmission electron microscopy analysis confirmed the formation of composites with different phases. The average crystallite size (D) values of pure Ag nanoparticles (NPs), ZnO NPs, and activated bentonite (Na-AB) were found to be 8.14, 18.1, and 37.6 nm, respectively. The Ag/bentonite NCs, ZnO/bentonite NCs, and Ag/ZnO/bentonite NCs exhibited the D values of 7.4, 9.4, and 9.4 nm, respectively. The Fourier transform infrared spectral analysis revealed the presence of hydroxyl, carbonyl, and other functional groups on the surface of the synthesized NCs. The transmission electron microscopic analysis revealed the formation of Ag and ZnO NPs with hexagonal, rod-shaped, and spherical structures. HRTEM also revealed the presence of (102) plane of ZnO and (220) plane of Ag in Ag/ZnO/bentonite NCs. The antibacterial activities of the composites suspension were evaluated against Escherichia coli ATCC 25922 and Staphylococcus aureus ATCC 25923 by the disc diffusion and broth dilution methods. The ternary NC and Ag/ZnO/bentonite exhibited better zone of inhibition of 14.3 ± 0.3 and 17.3 ± 0.2 mm at 10 mg·mL−1 toward E. coli and S. aureus bacterial strains. The minimum inhibitory concentration and minimum bactericidal concentration values of Ag/ZnO/bentonite NCs were found to be 156.25 and 312.5 µg·mL−1 for E. coli. The investigation results revealed that the low temperature bio-synthesized Ag/ZnO/bentonite is a promising bactericide over the binary composites.