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New hexadecylpiperidinium surfactants, containing one or two butylcarbamate fragments, were synthesized. The antimicrobial activity, toxicity, aggregation behavior in aqueous solutions, and solubilization capacity of these surfactants towards the hydrophobic drug ibuprofen were characterized. These surfactants demonstrated a high antimicrobial activity against a wide range of pathogenic bacteria, including both Gram-positive and Gram-negative strains, as well as fungi. By forming mixed-micellar compositions of the cationic surfactant 1-CB(Bu)-P-16 and the nonionic surfactant Brij®35, highly functional and low-toxic formulations were obtained. Furthermore, the transition from mixed micelles to niosomes was accomplished, enhancing their potential as drug delivery systems. Niosomes were found to be less toxic compared to mixed micelles, while also increasing the solubility of ibuprofen in water. The modification of niosomes with cationic surfactants made it possible to increase the stability of the system and improve the solubility of the drug. The data obtained indicate that these new carbamate-containing hexadecylpiperidinium surfactants have significant potential in biomedical applications, particularly in the formulation of advanced drug delivery systems.

New methodologies, rules, modalities, and procedures for the mechanism established under Article 6(4) of the Paris Agreement have led to the need to change the national conditions for the implementation of climate projects, including climate projects in forests. However, the issue of evaluating the effectiveness of such projects and their attractiveness to investors remains controversial, as their place and role in the modern economy remain uncertain. Therefore, the aim of the study was to assess the investment attractiveness and silvicultural feasibility of implementing reforestation climate projects in the central forest steppe of Russia. Thanks to mathematical models (including the developed coefficient of carbon intensity of investment costs) and the calculations carried out, it will be possible to develop a differentiated approach to assessing the investment attractiveness of climate projects’ implementation in forests. Reforestation projects including the planting of fast-growing tree species were considered. Maximum carbon sequestration for these projects is expected to occur over a period of 10–30 years. It was found that the coefficient of carbon intensity of investment costs, discounted by the duration of such projects, may become the basis for decision-making on investments in afforestation and reforestation in the central forest steppe.

A synthesis procedure and aggregation properties of a new homologous series of dicationic gemini surfactants with a dodecane spacer and two carbamate fragments (N,N′-dialkyl-N,N′-bis(2-(ethylcarbamoyloxy)ethyl)-N,N′-dimethyldodecan-1,6-diammonium dibromide, n-12-n(Et), where n = 10, 12, 14) were comprehensively described. The critical micelle concentrations of gemini surfactants were obtained using tensiometry, conductometry, spectrophotometry, and fluorimetry. The thermodynamic parameters of adsorption and micellization, i.e., maximum surface excess (Гmax), the surface area per surfactant molecule (Amin), degree of counterion binding (β), and Gibbs free energy of micellization (∆Gmic), were calculated. Functional activity of the surfactants, including the solubilizing capacity toward Orange OT and indomethacin, incorporation into the lipid bilayer, minimum inhibitory concentration, and minimum bactericidal and fungicidal concentrations, was determined. Synthesized gemini surfactants were further used for the modification of liposomes dual-loaded with α-tocopherol and donepezil hydrochloride for intranasal treatment of Alzheimer’s disease. The obtained liposomes have high stability (more than 5 months), a significant positive charge (approximately + 40 mV), and a high degree of encapsulation efficiency toward rhodamine B, α-tocopherol, and donepezil hydrochloride. Korsmeyer-Peppas, Higuchi, and first-order kinetic models were used to process the in vitro release curves of donepezil hydrochloride. Intranasal administration of liposomes loaded with α-tocopherol and donepezil hydrochloride for 21 days prevented memory impairment and decreased the number of Aβ plaques by 37.6%, 40.5%, and 72.6% in the entorhinal cortex, DG, and CA1 areas of the hippocampus of the brain of transgenic mice with Alzheimer’s disease model (APP/PS1) compared with untreated animals.

The xerogels based on the aqueous solutions of urea in potassium silicate liquid glass (PSLG) were produced by CO2 bubbling and investigated. The structure and chemical composition of the obtained materials were analyzed. Using the SEM, XRD, IR-FT, DSC, and low energy local EDS analysis, it was recognized that the dried gels (xerogels) contained three forms of urea: oval crystals of regular shape appeared onto the surface of xerogel particles; fibrous crystals were located in the silicate matrix; and molecules/ions were incorporated into the silicate matrix. It was shown that an increase in [(NH2)2CO] in the gel-forming system promoted increased contents in crystalline forms of urea as well as the diameter of the fiber-shaped urea crystals. A rate of the urea release in water from the granulated xerogels containing 5.8, 12.6, and 17.9 wt.% of urea was determined by the photometric method. It was determined that the obtained urea-containing xerogels were characterized with a slow release of urea, which continued up to 120 days, and could be used as controlled release fertilizers containing useful nutrients (N, K).

Low-temperature (350 °C) vitrification in a KNO3-NaNO3-KHSO4-NH4H2PO4 system, containing various additives to improve the chemical durability of the obtained material, was investigated. It was shown that a glass-forming system with 4.2–8.4 wt.% Al nitrate admixtures could form stable and transparent glasses, whereas the addition of H3BO3 produced a glass–matrix composite containing BPO4 crystalline inclusions. Mg nitrate admixtures inhibited the vitrification process and only allowed obtaining glass–matrix composites with combinations with Al nitrate and boric acid. Using ICP and low-energy EDS point analyses, it was recognized that all the obtained materials contained nitrate ions in their structure. Various combinations of the abovementioned additives favored liquid phase immiscibility and crystallization of BPO4, KMgH(PO3)3, with some unidentified crystalline phases in the melt. The mechanism of the vitrification processes taking place in the investigated systems, as well as the water resistance of the obtained materials, was analyzed. It was shown that the glass–matrix composites based on the (K,Na)NO3-KHSO4-P2O5 glass-forming system, containing Al and Mg nitrates and B2O3 additives, had increased water resistance, in comparison with the parent glass composition, and could be used as controlled-release fertilizers containing the main useful nutrients (K, P, N, Na, S, B, and Mg).

Amino- and carboxyl-functionalized carbon quantum dots (Amino-CQDs) were synthesized through fast and simple microwave treatment of a citric acid, ethylenediamine and ethylenediaminetetraacetic acid (EDTA) mix. The reproducible and stable optical properties from newly synthesized CQD dispersion with a maximum absorbance spectra at 330 nm and the symmetric emission maximum at 470 nm made the Amino-CQDs a promising fluorescence material for analytical applications. The highly aminated and chelate moieties on the CQDs was appropriate for a copper (Cu2+) cation sensor in the linear range from 1 × 10−4 mg/mL to 10 mg/mL with a limit of detection at 0.00036 mg/mL by static fluorescence quenching effects. Furthermore, Amino-CQDs demonstrated stable fluorescence parameters for assays in diluted alkali metal solution (Na+ and K+) and sea water. Finally, a visual sensor, based on Amino-CQDs, was successfully created for the 0.01–100 mg/mL range to produce a colorimetric effect that can be registered by computer vision software (Open CV Python).

Cerasomes are a promising modification of liposomes with covalent siloxane networks on the surface that provide outstanding morphological stability while maintaining all the useful traits of liposomes. Herein, thin film hydration and ethanol sol injection methods were utilized to produce cerasomes of various composition, which were then evaluated for the purpose of drug delivery. The most promising nanoparticles obtained by the thin film method were studied closely using MTT assay, flow cytometry and fluorescence microscopy on T98G glioblastoma cell line and modified with surfactants to achieve stability and the ability to bypass the blood–brain barrier. An antitumor agent, paclitaxel, was loaded into cerasomes, which increased its potency and demonstrated increased ability to induce apoptosis in T98G glioblastoma cell culture. Cerasomes loaded with fluorescent dye rhodamine B demonstrated significantly increased fluorescence in brain slices of Wistar rats compared to free rhodamine B. Thin film hydration with Tween 80 addition was established as a more reliable and versatile method for cerasome preparation. Cerasomes increased the antitumor action of paclitaxel toward T98G cancer cells by a factor of 36 and were able to deliver rhodamine B over the blood–brain barrier in rats.

Despite the many different methods for creating modified heat transfer surfaces to increase critical heat fluxes and heat transfer coefficients at pool boiling of various liquids at given reduced pressures, active research is currently underway to find optimal surface morphology and geometric parameters of structures for practical application. In this work, we used the method of microarc oxidation (MAO) to obtain coatings with different microstructures on the surface of duralumin heaters. In the present work, we studied the effect of MAO coatings on heat transfer, critical heat flux, and evaporation dynamics during liquid nitrogen boiling under conditions of steady-state heat release at pressures of 0.1, 0.05, and 0.017 MPa. It was shown that the modification of heaters led to a 50–60% increase in heat transfer coefficients as compared to the smooth one under the atmospheric pressure. Based on the data of high-speed video filming of boiling, it was shown that the main mechanism of intensification is the increase in quantity of active nucleation sites. A significant decrease in pressure led to the absence of a significant difference in both heat transfer intensity and evaporation dynamics for the smooth and modified heaters.

Typical non-metallic inclusions in two industrial low-carbon steels for oil pipelines were investigated as three-dimensional objects on film filters after electrolytic extraction and filtration of metal samples. A method of soft chemical extraction using a 10%AA electrolyte was used to study the initial corrosion process in the steel matrix surrounding various non-metallic inclusions. To determine and compare “corrosive” inclusions and their influence on the initial stages of corrosion of the adjacent layer of the steel matrix, quantitative parameters (such as the diameter of the corrosion crater (Dcr) and pit (Dpit), and the relative dissolution coefficient of the metal matrix (KD) around various inclusions) were determined after chemical extraction. It was found that CaO-Al2O3-MgO oxides and TiN inclusions did not cause an initial corrosion of the steel matrix surrounding these inclusions. However, tensile stresses in the steel matrix occurred around CaS inclusions (or complex inclusions containing a CaS phase), which contributed to the initiation of corrosion around these inclusions.

Low-grade waste heat harvesting and conversion into electric energy is an important way of renewable energy development and thermo-electrochemical cells are promising devices to solve this problem. In this paper, we report original data on the current density and maximum output power dependents on voltage of the thermos-cells with nickel hollow microspheres electrodes and different electrolyte concentration (from 0.1 to 3.0 mol/l)which exhibit excellent hypothetical Seebeck coefficient and accordingly high open-circuit voltage values at low source temperature. The composition, microstructure and morphology of the hollow nickel microspheres based electrodes are included here. Because of the low cost of nickel based thermo-cells could be commercially feasible for harvesting low-quality thermal energy, in this connection, the raw data of measurements of their properties are given here.The data is related to “High Seebeck coefficient thermo-electrochemical cell using nickel hollow microspheres electrodes”, Burmistrov et al., Renewable Energy, 2020 [1].

Carbon quantum dots (CQDs) are an excellent eco-friendly fluorescence material, ideal for various ecological testing systems. Herein, we establish uniform microwave synthesis of the group of carbon quantum dots with specific functionalization of ethylenediamine, diethylenetriamine, and three types of Trilon (A, B and C) with chelate claws -C-NH3. CQDs’ properties were studied and applied in order to sense metal cations in an aquatic environment. The results provide the determination of the fluorescence quench in dots by pollutant salts, which dissociate into double-charged ions. In particular, the chemical interactions with CQDs’ surface in the Irving–Williams series (IWs) via functionalization of the negatively charged surface were ascribed. CQD-En and CQD-Dien demonstrated linear fluorescence quenching in high metal cation concentrations. Further, the formation of claws from Trilon A, Trilon B, and C effectively caught the copper and nickel cations from the solution due to the complexation on CQDs’ surface. Moreover, CQD-Trilon C presented chelating properties of the surface and detected five cations (Cu2+, Ni2+, Ca2+, Mg2+, Zn2+) from 0.5 mg/mL to 1 × 10−7 mg/mL in the Irving–William’s series. Dependence was mathematically attributed as an equation (ML regression model) based on the constant of complex formation. The reliability of the data was 0.993 for the training database.

MXenes are an emerging family of two-dimensional (2D) early transition metal carbides/nitrides that are produced by selective A-element chemical etching from 3D MAX phase counterpart. Herein we report a low-cost method combining self-propagation high-temperature synthesis (SHS) and grinding to produce Ti3AlC2 precursor and further its usage to obtain Ti3C2Tx MXene. The SHS-ground precursor requires the same etching conditions as pressure-less synthesized precursors to fully etch A-layer and convert the 3D structure into 2D state. The obtained MXenes are atomically-thin flakes with an average lateral size of 1–2 μm. The room temperature electrical resistivity of Ti3C2Tx based 11 μm-thick film ranges between 295 and 317 μΩ·cm. SHS combining with grinding in one step can be considered as a scalable method to MXene synthesis. Keywords: MXenes, Self-propagation high-temperature synthesis, Chemical etching, Electrical conductivity

This review focuses on synthetic and natural amphiphilic systems prepared from straight-chain and macrocyclic compounds capable of self-assembly with the formation of nanoscale aggregates of different morphology and their application as drug carriers. Since numerous biological species (lipid membrane, bacterial cell wall, mucous membrane, corneal epithelium, biopolymers, e.g., proteins, nucleic acids) bear negatively charged fragments, much attention is paid to cationic carriers providing high affinity for encapsulated drugs to targeted cells. First part of the review is devoted to self-assembling and functional properties of surfactant systems, with special attention focusing on cationic amphiphiles, including those bearing natural or cleavable fragments. Further, lipid formulations, especially liposomes, are discussed in terms of their fabrication and application for intracellular drug delivery. This section highlights several features of these carriers, including noncovalent modification of lipid formulations by cationic surfactants, pH-responsive properties, endosomal escape, etc. Third part of the review deals with nanocarriers based on macrocyclic compounds, with such important characteristics as mucoadhesive properties emphasized. In this section, different combinations of cyclodextrin platform conjugated with polymers is considered as drug delivery systems with synergetic effect that improves solubility, targeting and biocompatibility of formulations.

The paper presents and discusses the results of the lithological, chronological and bio­stratigraphic study of the sediment sequence on Bolshoy Klimenetsky Island, the larg­est island within the Kizhi Archipelago. Inferred changes in sedimentation environments are related to the lake-level changes of Lake Onego in the Late and Postglacial times. At the earliest stage, the sedimentation took place in the Onego Ice Lake, when the lake level exceeded 80 m at the study site. Seasonally laminated clays accumulated at the bottom of the ice lake. Diatoms were substantially limited in both essential nutrients and light due to increased water turbidity. With the regression of the Onego Ice Lake ca. 11300 yrs BP the formation of micro-laminated clays started. The Lake Onego level drop prior to ~6500 yrs BP, presumably at the Early Holocene, resulted in the erosion of the older sediments. This was followed by the establishment of shallow-water coastal environments favoring the accumulation of sandy sediments and flourishing of benthic diatoms. At the following stage, low-energy environments gradually formed as a result of decreased hydrodynamic action and possibly some water-level rise due to increased climate humidity in the mid­Holocene. Silty sediments with a higher proportion of planktonic diatoms accumulated at the small shallow bay that existed at the study site. ~7000 yrs BP the Lake Onego lev­el was below ~40 m. As the regression proceeded, ~6500 yrs BP the Lake Onego level dropped to ~36-37 m, and organic sedimentation started in the sheltered bay, where epiphytic diatoms prevailed. ~6100 yrs BP the Lake Onego level dropped further to below ~36 m, resulting in the isolation of the study site and the onset of peat formation.

Iron powders and Fe/graphene oxide and Fe/boron nitride composites were synthesized by means of a polyol synthesis method. The effect of NaOH/Fe and ascorbic acid/Fe ratios on the characteristics of synthesized products were evaluated. The samples were characterized by X-ray diffraction, scanning and transmission electron microscopy, low-temperature nitrogen adsorption and Raman-spectroscopy. Ascorbic acid-assisted polyol synthesis resulted in the 10-fold decrease of the iron particles’ size and almost 2-fold increase of lead removal efficiency. The deposition of iron on the surface of graphene oxide lead to the formation of small 20−30 nm sized particles as well as bigger 200−300 nm sized particles, while the reduction in presence of boron nitride resulted in the 100−200 nm sized particles. The difference is attributed to the surface state of graphene oxide and boron nitride. Adsorption properties of the obtained materials were studied in the process of Pb2+ ion removal from wastewater.

Nickel oxide (NiO) is one of the most promising and high-performing Hole Transporting Layer (HTL) in inverted perovskite solar cells due to ideal band alignment with perovskite absorber, wide band gap, and high mobility of charges. At the same time, however, NiO does not provide good contact and trap-free junction for hole collection. In this paper, we examine this problem by developing a double hole transport configuration with a copper iodide (CuI) interlayer for efficient surface passivation. Transient photo-current (TPC) measurements showed that Perovskite/HTL interface with CuI interlayer has an improved hole injection; CuI passivation reduces the concentration of traps and the parasitic charge accumulation that limits the flow of charges. Moreover, we found that CuI protect the HTL/perovskite interface from degradation and consequently improve the stability of the cell. The presence of CuI interlayer induces an improvement of open-circuit voltage VOC (from 1.02 V to 1.07 V), an increase of the shunt resistance RSH (100%), a reduction of the series resistance RS (−30%), and finally a +10% improvement of the solar cell efficiency.

Corrosion rate in different steel grades (including oilfield pipeline steels) is determined by the presence of non-metallic inclusions (NMI) in steels. Specifically, the effect of different inclusions on the quality of steels depends on their characteristics such as size, number, morphology, composition, and physical properties, as well as their location in the steel matrix. Therefore, the optimization and control of NMI in steels are very important today to obtain an improvement of the material properties of the final steel products. It is well known that a Ca-treatment of liquid steels in ladle before casting is an effective method for modification of non-metallic inclusions for improvement of the steel properties. Therefore, the NMI characteristics were evaluated in industrial steel samples of low carbon Ca-treated steel used for production of oil-pipelines. An electrolytic extraction technique was used for extraction of NMI from the steel samples followed by three-dimensional investigations of different inclusions and clusters by using SEM in combination with EDS. Moreover, the number and compositions of corrosion active non-metallic inclusions were estimated in hot rolled steel samples from two different heats. Finally, the corrosion resistance of these steels can be discussed depending on the characteristics of non-metallic inclusions present in the steel.

The current study presents research into the effect of graphene oxide (GO) with a carbon to oxygen ratio of 4:1 on the fluidity, hydration, microstructure, mechanical and physical properties of Portland cement pastes and mortars. The amounts of GO investigated were 0.02%, 0.04%, and 0.06% by weight of cement, while for mortars, an extra composition with 0.1% was also prepared. According to the results, the fluidity of cement paste and mortar increased and the hydration process was slightly retarded with the addition of GO. Despite this, improvements in compressive and flexural strength were established in the mortars containing GO. The maximum effects (~22% and ~6%, respectively) were obtained with the addition of 0.06% GO. The calculation of estimated strength proportional to samples of equal density showed that for mortars cured for 7 days the gain in strength was directly related to the gain in density. For mortar samples cured for 28 days, the estimated strength was found to be significantly higher than that of the reference sample, indicating that besides density there are other factors determining the improvement in strength of mortars modified with GO. The possible structure strengthening mechanisms are discussed.