Carey Lea silver hydrosol is a rare example of very concentrated colloidal solutions produced with citrate as only protective ligands, and prospective for a wide range of applications, whose properties have been insufficiently studied up to now. Herein, the reactivity of the immobilized silver nanoparticles toward oxidation, sulfidation, and sintering upon their interaction with hydrogen peroxide, sulfide ions, and chlorocomplexes of Au(III), Pd(II), and Pt(IV) was investigated using SEM and X-ray photoelectron spectroscopy (XPS). The reactions decreased the number of carboxylic groups of the citrate-derived capping and promoted coalescence of 7 nm Ag NPs into about 40 nm ones, excluding the interaction with hydrogen peroxide. The increased nanoparticles form loose submicrometer aggregates in the case of sulfide treatment, raspberry-like micrometer porous particles in the media containing Pd(II) chloride, and densely sintered particles in the reaction with inert H₂PtCl₆ complexes, probably via the formation of surface Ag-Pt alloys. The exposure of Ag NPs to HAuCl₄ solution produced compact Ag films along with nanocrystals of Au metal and minor Ag and AgCl. The results are promising for chemical ambient temperature sintering and rendering silver-based nanomaterials, for example, for flexible electronics, catalysis, and other applications.

A new approach is being considered for obtaining microfibrillated cellulose with a low degree of polymerization by sulfuric acid hydrolysis with simultaneous ultrasonic treatment under mild conditions (temperature 25 °C, 80% power control). Samples of initial cellulose, MCC, and MFC were characterized by FTIR, XRF, SEM, DLS, and TGA. It was found that a high yield of MFC (86.4 wt.%) and a low SP (94) are observed during hydrolysis with ultrasonic treatment for 90 min. It was shown that the resulting microfibrillated cellulose retains the structure of cellulose I and has an IC of 0.74. It was found that MFC particles are a network of fibrils with an average size of 91.2 nm. ζ-potential of an aqueous suspension of MFC equal to −23.3 mV indicates its high stability. It is noted that MFC has high thermal stability, the maximum decomposition temperature is 333.9 °C. Simultaneous hydrolysis process with ultrasonic treatment to isolate MFC from cellulose obtained by oxidative delignification of spruce wood allows to reduce the number of stages, reduce energy costs, and expand the scope.

Surface nanobubbles at hydrophobic interfaces now attract much attention in various fields but their role in wetting-related phenomena is still unclear. Herein, we report the effect of a preliminary contact of “hot” solids with cold water previously proposed for generation of surface nanobubbles, on wettability of compact materials and flotation of particulate galena (PbS), sphalerite (ZnS), and Pb-Zn sulfide ore. Atomic force microscopy was applied to visualize the nanobubbles at galena crystals heated in air and contacted with cold water; X-ray photoelectron spectroscopy was used to characterize the surface composition of minerals. Contact angles measured with the sessile drop of cold water were found to increase when enhancing the support temperature from 0 to 80 °C for sphalerite and silica, and to pass a maximum at 40–60 °C for galena and pyrite (FeS₂) probably due to oxidation of sulfides. The temperature pretreatment depressed the recovery of sulfides in collectorless schemes and improved the potassium butyl xanthate-assisted flotation both for single minerals and Gorevskoye Pb-Zn ore. The results suggest that the surface nanobubbles prepared using the temperature difference promote flotation if minerals are rather hydrophobic and insignificantly oxidized, so the addition of collector and activator (for sphalerite) is necessary.

Due to their unique properties, organosols of silver nanoparticles are widely used in optical and semiconductor devices, to produce electrically and thermally conductive films, as catalysts, antibacterial materials, etc. This work proposes a simple and highly productive method for the preparation of silver organosols, which have a metal concentration as high as 1800 g/L and contain spherical nanoparticles with low polydispersity and a median size of 9.1 nm. The method consists in the initial preparation of silver nanoparticle hydrosols with a concentration of higher than 30 g/L followed by the transfer of the NPs into an organic phase of o -xylene. A set of physical research methods has been employed to study the regularities of the extraction of silver nanoparticles with o -xylene in the presence of cetyltrimethylammonium bromide (CTAB) and ethanol and to determine the optimal process conditions, under which the extraction degree is as high as 62.5%. It has been found that bromine anions contained in CTAB molecules cause the aggregation of some amount of silver nanoparticles with the formation of silver metal sediment in the aqueous phase. According to X-ray photoelectron spectroscopy data, the sediment contains bromide ions (up to 4 at %) on the particle surface. Organosols synthesized under optimal conditions are stable for more than 7 months and withstand repeated cycles of drying and redispersing. Silver organosols have been used to obtain metal films with an electrical conductivity of about 68 500 S/cm, which increases to 412 000 and 509 500 S/cm (87.8% of the electrical conductivity of bulk silver) after thermal treatment at 150 and 250°C, respectively.

We report here the application of the low-temperature X-ray photoelectron spectroscopy (cryo-XPS) of fast-frozen dispersions as a quasi in situ technique for a case study of metal sulfides reacted in acidic aqueous solutions under non-oxidizing and moderate oxidizing conditions. The sulfide surfaces are known to tend to be depleted in metals, producing essentially sulfur-enriched surfaces and extended underlayers on Fe- and Cu-bearing sulfides, which have previously been examined using depth-sensitive HAXPES and cryo-XPS. The current study is focused on zinc and lead sulfides (natural sphalerite and galena), for whom both the experiment and theoretical DFT simulations suggest a low stability of sulfur-excessive structures. Cryo-XPS revealed the complicated behavior of the minerals under non-oxidative etching conditions, in particular, a notable concentration of polysulfide for PbS in dilute perchloric acid and a very minor one in hydrochloric acid. Oxidative etching with Fe³⁺ cations produced polysulfide anions and then elemental sulfur, which both volatized in the ultra-high vacuum at room temperature; the species can, nonetheless, be distinguished by considering the binding energies, electrostatic charging and evaporation rates. The cryo-XPS also detected interfacial products, e.g., ferrous chloride. DFT found that S-excessive centers are unstable in the undersurface regions of both materials, but are less unfavorable for ZnS surfaces, in agreement with the experimental data. It was concluded that cryo-XPS allows us to greatly reduce distortions of the interface composition in comparison with conventional techniques.

XPS, PbL3 and CuK EXAFS, solid state NMR, and EPR techniques are used to study insoluble products formed in the interaction of aqueous solutions of lead(II) nitrate and copper (II) sulfate with potass