Structural Units Research Articles

Anatomy of a fumarole field: drone remote-sensing and petrological approaches reveal the degassing and alteration structure at La Fossa cone, Vulcano, Italy

Abstract. Hydrothermal alteration and mineralization processes can affect the physical and chemical properties of volcanic rocks. Aggressive acidic degassing and fluid flow often also lead to changes in the appearance of a rock, such as changes in surface coloration or intense bleaching. Although hydrothermal alteration can have far-reaching consequences for rock stability and permeability, limited knowledge exists on the detailed structures, extent, and dynamic changes that take place near the surface of hydrothermal venting systems. By integrating drone-based photogrammetry with mineralogical and chemical analyses of rock samples and surface gas flux, we investigate the structure of the evolving volcanic degassing and alteration system at the La Fossa cone on the island of Vulcano, Italy. Our image analysis combines principal component analysis (PCA) with image classification and thermal analysis through which we identify an area of approximately 70 000 m2 that outlines the maximum extent of hydrothermal alteration effects at the surface, represented by a shift in rock color from reddish to gray. Within this area, we identify distinct gradients of surface coloration and temperature that indicate a local variability in the degassing and alteration intensity and define several structural units within the fumarole field. At least seven such larger units of increased activity could be constrained. Through mineralogical and geochemical analysis of samples from the different alteration units, we define a relationship between surface appearance in drone imagery and the mineralogical and chemical composition. Gradients in surface color from reddish to gray correlate with a reduction in Fe2O3 from up to 3.2 % in the unaltered regime to 0.3 % in the altered regime, and the latter coincides with the area of increased diffuse acid gas flux. As the pixel brightness increases towards higher alteration gradients, we note a loss of the initial (igneous) mineral fraction and a change in the bulk chemical composition with a concomitant increase in sulfur content from close to 0 % in the unaltered samples to up to 60 % in samples from the altered domains. Using this approach of combined remote-sensing and in situ analyses, we define and spatially constrain several alteration units and compare them to the present-day thermally active surface and degassing pattern over the main crater area. The combined results permit us to present a detailed anatomy of the La Fossa fumarole field, including high-temperature fumaroles and seven larger units of increased alteration intensity, surface temperature, and variably intense surface degassing. Importantly, we also identify apparently sealed surface domains that prevent degassing, likely as a consequence of mineral precipitation from degassing and alteration processes. By assessing the thermal energy release of the identified spatial units quantitatively, we show that thermal radiation of high-temperature fumaroles accounts for < 50 % of the total thermal energy release only and that the larger part is emitted by diffuse degassing units. The integrated use of methods presented here has proven to be a useful combination for a detailed characterization of alteration and activity patterns of volcanic degassing sites and has the potential for application in alteration research and for the monitoring of volcanic degassing systems.

The Combined Effect of Taproot and Fibrous Roots of Herbaceous Plants and Shrubs on the Distribution of Soil Water-Stable Aggregates

Soil aggregation, an important indicator of soil restoration in degraded ecosystems, is a fundamental unit of soil structure. However, research on the influence of grass–shrub composites on the distribution of >0.25 mm soil water-stable aggregates (macroaggregates) is scarce. Therefore, this study focuses on the hill and gully region of the Loess Plateau, where vegetation has been well restored since the return of farmland to forests and grasslands. The study investigated the root and macroaggregate distribution characteristics and interrelationships of three widely distributed mixed vegetation types of Caragana korshinskii and Agropyron cristatum (C-AC), C. korshinskii and Bothriochloa ischaemum (C-BI), and C. korshinskii and Artemisia gmelinii (C-AG) in this area. The results indicate that soil macroaggregates decrease with increasing depth. Due to the spatial differences in the distribution of shrub root, the content of macroaggregates at 50 cm from the shrub base was higher than that at the shrub base, with an increase of 25.98%–34.27% in different vegetation associations. In this study, the root length density and root diameter better reflected the influence of roots on the distribution of macroaggregates, and the product of the two had a good power function relationship with the content of macroaggregates (R2 ≥ 0.82, p < 0.01). Grey correlation analysis showed that the influence of root length density on the distribution of large aggregates was greater than that of root diameter. The content of macroaggregates in the vegetation association of taproot herbaceous plants and shrubs was higher than that of fibrous root herbaceous plants. The average soil macroaggregate content in the C-AG was 15.79%–248.6% higher than that in the C-BI and C-AC. In this study, the spatial distribution differences in root caused by shrub growth were the main reason for the spatial heterogeneity of soil macroaggregate content distribution. The improvement ability of soil macroaggregates was higher in the combination of taproot herbaceous plants and shrubs than in the combination of fibrous root herbaceous plants and shrubs. The results of this study can, to some extent, reveal the influence and mechanisms of plant roots on soil aggregates in grass–shrub vegetation association.

An Analysis of Structural Units and Modification of the Idiomatic Expressions on Speech Videos

This research analyzed idiomatic expressions in speech videos on the TEDx Talks YouTube channel. This study used descriptive linguistics to collect qualitative data and used analytical techniques. The data were taken from nine speech videos from TEDx Talks YouTube channel, after collected the idiomatic expressions, the data were categorized using two theories: Biber’s (1999) and Ernst’s (1981) theories. This study found 54 kinds of structural units of idiomatic expressions with the most dominant were prepositional phrase idioms with total 21 idioms, followed by selected verb + noun phrase idioms with total 14 idioms, next selected verb + prepositional phrase idioms with total 13 idioms, and lastly noun phrase idioms with total 6 idioms. This study also found 11 idiom modifications, and internal modifications were the most appeared with total 5 idioms, followed by external modifications with total 4 idioms, and lastly conjunction modification with total 2 idioms. The implications of this research can be used in teaching and learning for EFL/ESL.

Asymmetric Synthesis of Chiral Cyclopropanes from Vinyl Sulfoxonium Ylides Catalyzed by a Chiral-at-Metal Rh(III) Complex.

A chiral-at-metal Rh(III) complex-mediated [2+1] cyclization of vinyl sulfoxonium ylides with α,β-unsaturated 2,2-acylimidazoles has been demonstrated for the first time. This work provides a practical approach for assembling 1,2,3-trisubstituted chiral cyclopropane with alkyl structural units, which had advantages such as a wide range of substrates, good functional group tolerance, and mild reaction conditions. In addition, further amplification experiments and transformation of cycloaddition products were carried out to highlight the practicality of the method.

Preparation and structure of titanium‐containing pyrophosphate glasses prepared using the liquid‐phase method

AbstractPhosphate invert glasses (PIGs) exhibit excellent biocompatibility because of their high chemical durability and controlled ion releasability. PIGs are composed of short phosphate units such as ortho‐ and pyrophosphate. This structure makes it difficult to obtain clear glass using the melt‐quenching method. Our previous work reported that intermediate oxides (such as TiO2 and Nb2O5)‐containing PIGs exhibit good glass‐forming ability and ion dissolution controllability. This work used a liquid‐phase method to prepare PIGs at room temperature and pressure. Furthermore, TiO2 was used to control ion releasability for biomedical applications. Titanium‐containing PIGs were successfully prepared using a liquid‐phase method. Pyrophosphate and titania formed P‐O‐Ti bonds with an increasing TiO2 content in the glass, forming chain‐like structural units such as (‐O‐P‐O‐P‐O‐Ti‐O‐)n. The number of chain‐like structures increased with an increasing TiO2 content in the glass, improving the chemical durability. Hence, the ion releasability of titanium‐containing PIGs prepared using the liquid‐phase method can be controlled by the glass structure. Additionally, the PIGs exhibited good cell viability. Therefore, the PIGs are candidates for carriers of therapeutic inorganic ions for biomedical applications.

Flexible curved multi-functional sensors for air flow and vibration signal measurement of train bogie

Abstract The fluid-solid coupling effects with the aerodynamic noise and structural vibration signal have great part in measurement accuracy and fault diagnosis of the train bogie. It is important to collect aerodynamic noise and structural vibration data for safety evaluation and on-line structural health monitoring (SHM) of the bogie, which brings new challenges to the integration and installation of the sensors in the limited space and complicated operation condition of the train bogie. Flexible curved multifunctional sensors (FCMFS) integrated with the hot film and structural vibration sensor units is designed to the air flow and structural vibration measurement of the train bogie. Bogie vibration and wind tunnel test platforms with FCMFS are built to the air flow velocity and vibration data measurement on the bogie surface under different operation conditions. Piezoelectric Polyvinylidene fluoride(PVDF) sensors have significant output in the wind tunnel and vibration experiments, and the hot film sensor is only sensitive to the air flow signal. The effect of vibration signal to the hot film sensor could be ignored, which is applied to decouple the aerodynamic noise and structural vibration signals for improving the measurement accuracy of the train bogie. The dynamic performance of FCMFS is verified in Rail Transmit Base of East China Jiaotong University, which is applied to SHM and rapid fault diagnosis of train bogie. The air flow distribution and vibration data are collected to safety assessment and fault diagnosis of train bogie, which would promote the intelligent maintenance level of the train bogie.

Electronic regulation of Ce,F-Ni2P/CoP catalyst for efficient water splitting

Designing efficient non-precious-metal bifunctional electrocatalysts is still challenging at present. Herein, the efficient Ce,F-Ni2P/CoP electrocatalyst for water splitting was successfully fabricated. As shown from the present investigation, the codoping of Ce and F in Ni2P/CoP induced the f-p-d gradient orbital coupling in the Ce-F-metal structural unit of the catalyst, significantly reducing the work function of the catalyst, which accelerated the reaction kinetics and improved the intrinsic catalytic activity. The catalyst exhibited the outstanding hydrogen evolution reaction (HER) activity in the full pH range and, especially in alkaline electrolyte, an ultra-low oxygen evolution reaction (OER) overpotential of 243 mV at 50 mA·cm−2 and an excellent HER overpotential of 88 mV at 10 mA·cm−2 were achieved. Moreover, Ce,F-Ni2P/CoP displayed an excellent overall water splitting (OWS) performance with η10 = 1.52 V. DFT theoretical calculations also showed that the gradient orbital coupling resulted in the reduction of the work function of the catalyst. Our work provides a new understanding of designing and constructing high-performance catalysts.

Influences of symmetric tilt grain boundary on the stretching deformation behaviors of Cu bicrystals

The microstructure of grain boundary (GB) becomes an important factor affecting the strength of nanomaterials during plastic deformation. In this work, Cu bicrystals with different coincidence site lattice (CSL) interfaces are constructed, and the influences of the symmetric tilt interface on the mechanical properties and plastic deformation behaviors during uniaxial tension are studied by molecular dynamics simulation. The results indicate that the peak stress of tensile stress-strain curves for most bicrystals is lower than its monocrystalline samples, except CSL3, CSL11 and CSL57 bicrystals with a continuous and single structural unit. The CSL3 bicrystal has the highest strength, while CSL33 bicrystal has the lowest strength among all the tested samples. The CSL11 and CSL57 bicrystals with a lower GB energy have a higher stability of interface, which delays the yielding. Moreover, the generation of twin and stair-rod dislocation at the interfaces strengthens the CSL11 and CSL57 bicrystals. The CSL3 almost has the same parameters as its monocrystalline sample S3, massive research has confirmed that the sample with a higher density twin (CSL3 interface) exhibits higher combined properties of strength and plasticity. This work may provide a guideline for GB engineering to improve material properties by controlling the GB structure.

Photocatalytic Regioselective Redox-Neutral 1,3-Oxypyridylation of Aryl Cyclopropanes.

Pyridines and cyclopropanes are important structural units in chemistry. Herein, we introduce a photoredox-catalyzed approach for the ring opening and 1,3-oxypyridylation of aryl cyclopropanes using 4-cyanopyridines and carboxylic acids. This sequential process involves single-electron oxidation of the aryl cyclopropane, leading to nucleophilic ring opening and radical pyridylation at the benzylic position. The redox-neutral reaction exhibits high regioselectivity under mild reaction conditions, offering a broad substrate scope and wide applicability.

Pressure-induced phase changes in natural fluorapophyllite-(K) studied by Raman spectroscopy

The high-pressure Raman spectra in the low-wavenumber region (50–1200 cm−1) and the hydroxyl stretching vibration region (2600–3800 cm−1) of fluorapophyllite-(K) were collected in the interval of 0.0–50.7 GPa. Experimental results show that fluorapophyllite-(K) undergoes a crystalline-crystalline phase transition from a tetragonal structure (P4/mnc) to an orthorhombic structure (Pnnm) and then amorphization under high pressure conditions. Discontinuous changes in Raman peaks in the hydroxyl vibration region (2600–3800 cm−1) and the low-wavenumber region (50–1200 cm−1) occur at different onset pressures, suggesting that the destabilization of sub-lattices in fluorapophyllite-(K) under high pressure is not synchronous; the weak interlayer H2O structural units are more prone to destabilization at lower pressures than the rigid SiO4 tetrahedral layer units. Therefore, H2O groups in fluorapophyllite-(K) serve as sensitive local probes during the pressure-induced phase transition and amorphization.

Chestnut soil organic carbon is regulated through pore morphology and micropores during the seasonal freeze–thaw process

Soil aggregates are basic structural units in soil organic carbon (SOC) protection. In alpine ecosystems, the seasonal freeze–thaw (FT) process characterizes soil formation and nutrient cycling. However, previous studies were mostly based on simulated FT experiments, which amplified the effects of natural FT processes. And, the regulations of pore structure on SOC protection/loss of aggregates during the FT processes were still not well understood. To investigate the effect of the seasonal FT process on SOC and pore structure of aggregates, as well as the interactions among them, soil samples were selected during a whole seasonal FT cycle, which can be divided into four periods: unstable freezing (UFP), stable frozen (SFP), unstable thawing (UTP), and stable thawed periods (STP). The results demonstrated that freezing increased SOC concentration as the total organic carbon (TOC) content of all aggregate fractions peaked in the SFP (17.46 g/kg on average). The TOC content of aggregates in the UFP dropped to 7.91 g/kg on average, which revealed a dramatic SOC loss after thawing began. Thawing also decreased the proportions of particulate organic carbon (POC) compared with mineral-associated organic carbon (MAOC). The highest microbial abundance was also found in the SFP. Freezing promoted the formation of pores > 80 μm while thawing increased the regularity of pore morphology. Pore structure explained 48.77 % of the SOC variance in the thawing period, but only 19.29 % of that in the freezing period. Overall, in the freezing process, soil pore structure impacted the SOC input by mediating pore morphology. In the thawing process, soil pore structure inhibited SOC loss by enhancing the formation of pores < 15 μm. These results demonstrate new perspectives on the soil aggregate microstructure–microbe–SOC interactions.

Mixed former effect in barium borophosphate glasses on the red (Eu3+)-blue (Eu2+) emission for LEDs

The synergistic mixing of P2O5 and B2O3 glass formers at a constant concentration of BaO as a glass modifier plays a vital role in generating a single-phase phosphor doped with Eu2O3 for white light-emitting diodes (WLEDs). Herein, a glass system of nominal composition xP2O5∙(50-x)B2O3∙49.5BaO∙0.5Eu2O3 (0 ≤ x ≤ 50 mol%) was prepared using a melt-quenching technique under normal atmospheric conditions. While the XRD patterns demonstrated the amorphous nature, the SEM micrographs proved the formation of cluster structures. Structural characterization using ATR-FTIR spectroscopy revealed the presence of main vibrational structural units associated with borate and phosphate glass formers, including BO3, BO4−, P=O, PO2−, and PO32−. The IR spectra at x = 0 and 50 mol% exhibit characteristic metaborate and metaphosphate absorption peaks, respectively. In contrast, the mixing of both B2O3 and P2O5 at equal concentrations (x = 25 mol%) has resulted in the absence of absorption peaks assigned to the BO3 and P=O units, thus indicating the mixed structural effect. This is assigned to the formation of B-O-P bonds, with the BO4−, PO2−, and PO32− as the main structural units. These structural changes affect the reduction process of Eu3+ to Eu2+, as demonstrated by the corresponding photoluminescence spectra and observed by the cathodoluminescence micrographs. Photoluminescence studies showed tunable emission from red (Eu3+) to white light (Eu2+ and Eu3+) under UV excitation, with the P2O5 content rising from 0 to 50 mol% due to the growing Eu2+ population formed by the reduction of Eu3+. The optical basicity was observed to decrease with the P2O5 content, favouring the reduction process. The demonstrated tunable single-host white phosphor makes this an attractive system for energy-efficient WLED applications.

Investigation on luminescent characteristics of Tb3+/Dy3+co-doped boro-phosphate glass for cool white LED and radiation shielding applications

The Tb3+/Dy3+ co-doped Boro-Phosphate Glass (BPANZDyTb) was produced (40 B2O3 + 39P2O5 + 5 Al2O3 + 5 NaF + 10 ZnO + 0.5 Tb2O3 + 0.5 Dy2O3) using melt-quenching technique. X-ray diffraction measurements, Raman, and Fourier Transform Infrared were used to evaluate the structural behavior of the prepared glass. Powder-XRD spectra, in the 10–90° range showed that the prepared glass was amorphous. FTIR analysis reveals that the network contains a variety of structural groups, including B-O-B, BO4, BO, P-O, PO2, P-O-B, and PO4 units. The UV–visible diffuse reflectance spectroscopy was used to record and study the optical linear properties of Tb3+/Dy3+ co-doped Boro-Phosphate Glass (BPANZDyTb). The photoluminescence excitation peak was obtained at 348 nm. The emission peaks were located at 484 nm (4F9/2 → 6H15/2 → blue), 576 nm (4F9/2 → 6H13/2 → yellow), and 662 nm (4F9/2 → 6H11/2 → red). Tb3+ ions are located at 412 nm (5D3 → 7F5), 441 nm (5D3 → 7F4), 546 nm (5D4 → 7F5), and 625 nm (5D4 → 7F3). The result of CIE 1931 chromaticity coordinates indicate that the prepared glass is suitable material for cold white light emitting diode applications due to its color coordinates x = 0.3106 and y = 0.3240 and correlated color temperature (CCT) values about 6768 K. The gamma-ray parameters such as half-value layer (HVL), mass attenuation coefficient (μ/ρ), mean free path (MFP), and effective atomic number (Zeff) of the BPANZDyTb glass were studied using Phy-X software. The results of the gamma-ray parameter show that the Dy3+ ions and Tb3+ ions co-doped BoroPhosphate glass is an appropriate material for radiation shielding applications.

Switch Capacitor–Based High Step‐Up Three‐Port DC–DC Converter for Fuel Cell/Battery Integration

ABSTRACTAddressing issues of low input voltage in new energy generation systems such as fuel cells, a high step‐up three‐port DC–DC converter for fuel cell/battery hybrid power supply system is proposed. The proposed converter is evolved from Boost three‐port converter, and switch capacitor structure and diode capacitor voltage doubling unit are employed to achieve high voltage gain and low voltage stress. The three ports are connected to fuel cell, battery and load respectively, among which the flow of energy is realized. The steady state performance of this converter in various operating states and design of parameter are presented. Primary competitive advantages compared to similar converters include high voltage gain, continuous input current and its feature of common ground. Moreover, control strategy and compensators under three operating modes are designed to achieve stable output voltage and battery protection. Finally, a 100 W experimental prototype with 15 V input voltage and 24 V battery voltage is established to verify the stable and dynamic performance of the proposed converter.

Molecularly Woven Cationic Covalent Organic Frameworks for Highly Selective Electrocatalytic Conversion of CO2 to CO.

Coupling carbon capture with electrocatalytic carbon dioxide reduction (CO2R) to yield high-value chemicals presents an appealing avenue for combating climate change, yet achieving highly selective electrocatalysts remains a significant challenge. Herein, two molecularly woven covalent organic frameworks (COFs) are designed, namely CuCOF and CuCOF+, with copper(I)-bisphenanthroline complexes as building blocks. The metal-organic helical structure unit made the CuCOF and CuCOF+ present woven patterns, and their ordered pore structures and cationic properties enhanced their CO2 adsorption and good conductivity, which is confirmed by gas adsorption and electrochemical analysis. In the electrocatalytic CO2R measurements, CuCOF+ decorated with extra ethyl groups exhibit a main CO product with selectivity of 57.81%, outperforming the CuCOF with 42.92% CO at the same applied potential of 0.8 VRHE. After loading Pd nanoparticles, CuCOF-Pd and CuCOF+-Pd performed increased CO selectivity up to 84.97% and 95.45%, respectively. Combining the DFT theoretical calculations and experimental measurements, it is assumed that the molecularly woven cationic COF provides a catalytic microenvironment for CO2R and ensures efficient charge transfer from the electrode to the catalytic center, thereby achieving high electrocatalytic activity and selectivity. The present work significantly advances the practice of cationic COFs in real-time CO2 capture and highly selective conversion to value-added chemicals.

Exploring the impact of CuCl2 modification on structural variations and dielectric constant in bismuth borate tellurite glasses

Copper chloride doped boro-tellurite-based glass series with compositions 60TeO2-(25-x) Bi2O3–15B2O3-xCuCl2 (x = 0, 5, 10, 15, and 20) were synthesized using the traditional melt-quench procedure. The X-ray diffraction patterns of the examined glasses reveal their amorphous nature. The effect of CuCl2 addition on the glass network/structural units was studied using vibrational (FTIR/Raman) spectroscopy, and CuCl2 inclusion in the glass matrix resulted in a transformation from compact TeO4 to TeO3 structural units This shows that copper chloride acts as a modifier in the examined glass series, resulting in the creation of non-bridging oxygen (NBOs), meaning that the loosening of the glass network is further supported by a decrease in the glass transition temperature as CuCl2 content increases. UV–Vis DRS spectra of examined glasses reveal an absorption band corresponding to the typical transition of Cu2+ ions from 2B1g → 2B2g, situated in deformed octahedral sites in absorption spectra. As Cu+ concentration rises, the indirect optical band gap values drop from 2.94 eV to 1.75 eV. The metallization criterion values lie between 0.383 and 0.300 suggesting that these glasses are potential candidates for nonlinear optical applications. With an increase in Cu+ concentration, the values of molar refractive index (Rm) and molar electronic polarizability αm increases from 22.412 to 26.205 and 8.894 to 10.398 respectively, which correlate with increasing dielectric constant (ε′) values as the Cu+ amount increases. Further dielectric studies reveal non-Debye-type relaxation behaviour.

Thermodynamics and kinetics of cation partitioning between plagioclase and trachybasaltic melt in static and dynamic systems: A reassessment of the lattice strain and electrostatic energies of substitution

Most of the solidification history of magmas beneath active volcanoes takes place in chemically and physically perturbed plumbing systems where the growth of crystals is collectively governed by a range of kinetic processes related to the dynamics of crustal reservoirs and eruptive conduits. In this context, we have experimentally investigated the partitioning of major, minor, and trace cations between plagioclase and trachybasaltic melt under conventional static (no physical perturbation) and dynamic (melt stirring) crystallization regimes. Slow interface reaction kinetics are established between the advancing crystal surface and the adjacent melt, as the result of the combined control of a small degree of effective undercooling, prolonged diffusive relaxation, and convective homogenization. The kinetic aspects of plagioclase growth influence the partitioning of trace cations during transport of structural units across the crystal-melt interface, with consequent departure from macroscopic equilibrium in the system. The type and number of charge–balanced and −imbalanced configurations produced by the accommodation of trace cations into the coordination polyhedron can be thermodynamically rationalized in terms of lattice strain and electrostatic partitioning energetics. However, the overall solution energy accompanying trace cation kinetic substitutions cannot be entirely deconvoluted from major component activities in both melt and plagioclase phases. The emerging view that slow interface kinetic processes may lead to strong compositional dependence for the partition coefficient in dynamic subvolcanic environments contrasts markedly with the conventional idea that the energetics of cation partitioning are dominantly controlled by the effect of isothermal changes in the bulk system.

Aggregation-Induced Enhanced Electrochemiluminescence Resonance Energy Transfer Biosensor for Ultrasensitive Detection of Carcinoembryonic Antigen Based on Donor-Acceptor Organic Nanoparticles.

Aggregation-induced electrochemiluminescence (AIECL) combines the merits of aggregation-induced emission (AIE) and electrochemiluminescence (ECL), which has become a research hot spot in recent years. Therefore, we synthesized a novel AIE compound (Z)-3-(4-(2-butyl-1,3-dioxo-2,3-dihydro-1H-benzo[de]isoquinolin-6-yl)phenyl)-2-(4-(1,2,2-triphenylvinyl)phenyl)acrylonitrile (TPENI) with a donor-acceptor (D-A) structure, that is, a simple peripheral modification of 4-(2-butyl-1,3-dioxo-2,3-dihydro-1H-benzo[de]isoquinolin-6-yl) benzaldehyde (NI-CHO) with AIE-active tetraphenylethylene (TPE) to achieve the transition of NI-CHO from aggregation-caused quenching (ACQ) to an AIE molecule. When TPENI was in the aggregated state, the luminescence intensity was significantly enhanced due to the TPE structural unit restricting the free rotation of the intramolecular benzene ring, as well as the π-π stacking interactions of the molecules, which was conducive to the preparation of TPENI NPs as ECL materials. Satisfactorily, we found that the ECL intensity of TPENI NPs was increased by about 4.8-fold compared with that of the molecules dispersed in organic solution, and the stability reached about 1000 s. Based on the excellent ECL properties of TPENI NPs, an "on-off-on" ECL biosensor with a wider detection range (1 fg/mL to 100 ng/mL) and a lower detection limit of 0.20 fg/mL (S/N = 3) was proposed for sensitive analysis of a carcinoembryonic antigen (CEA). Overall, this work provided a new approach to the realization of AIECL and laid the foundation for the application of naphthalimide derivatives in ECL.

Densification and network structural changes in binary aluminosilicate glass via cold sintering process

Binary aluminosilicate glasses containing 20–50 wt% Al2O3 were successfully densified through a cold sintering process (CSP) using 1–10 M NaOH solutions. The investigation focused on densification and structural unit changes in the cold-sintered binary aluminosilicate glasses. Specifically, the binary aluminosilicate glass with 40 wt% Al2O3, cold-sintered at 180 °C using 1–10 M NaOH solutions, achieved a relative density of up to 90 % at 10 M NaOH. This was attributed to an enhanced dissolution-precipitation process facilitated by an increased concentration of the NaOH solution. In aluminosilicate glasses with 20–50 wt% Al2O3, the relative densities approached 90 % after CSP at 180 °C using a 10 M NaOH solution. Al(OH)3 formation in the cold-sintered glasses was confirmed, particularly at higher concentrations of NaOH solution (>10 M) and higher contents of Al2O3 (>40 wt%). Changes in Si structural units were observed during CSP, with Al-rich Si units becoming dominant as the concentration of the NaOH solution increased. The higher substitution of Si-O-Si bonds by Si-O-Al bonds led to the precipitation of Al(OH)3, as well as an increased Vickers hardness and biaxial flexural strength of the cold-sintered glasses. These findings demonstrate that the Al2O3 content and NaOH concentration play important roles in the densification and enhancement of the mechanical property in the cold-sintered alumina-rich binary aluminosilicate glasses and offer insights into the optimal conditions for obtaining desirable aluminosilicate materials through CSP.

POWER SUPPLY UNIT OF THE STAND AND LABORATORY INSTALLATION FOR TREATING OLIVES WITH ELECTROSTATIC FIELD

Most technological machines (TM) use hydraulic drives and internal combustion engines, such as lifting and transporting, loading and unloading, construction, road, track, and mining. Increasing the durability of the specified TM units is an urgent task. One of the possible solutions to this urgent problem is the electrostatic treatment of hydraulic oils and diesel fuels. Over the past three decades, researchers have conducted many studies focused on finding optimal means of using external force fields to improve the quality of lubricating materials and intensify their production. Types of influence of force fields, such as mechanical, mechanochemical, acoustic, electromagnetic, and electric, are increasingly used to regulate the behaviour of dispersed particles in nonpolar and slightly polar environments. The theory of regulated interphase transitions proves that the emergence, growth, and size change of supramolecular structures, surrounded by an adsorption-solvate layer and creating complex structural units in oil dispersion systems, contribute to the emergence of new properties of these systems. One of the main provisions of this theory is the need for extreme and antibating changes in the size of complex structural units with the help of external influences, which include force fields. Lubricating materials differ in their degrees of dispersity, composition, and properties, so the effect of force fields on them is diverse. The ability to regulate intermolecular interactions and the size of complex structural units are significant in the operation of lubricants. Electric fields make it possible to control phase interactions in these dispersed systems: they increase the constant dipole moments of particles and the electrosurface forces, which contribute to the deformation of the electric double layer. Under the action of strong electric fields, structural changes occur in hydrocarbon dispersion systems, which significantly change the physicochemical properties of lubricating materials. Thus, the dynamic viscosity of the lubricant and its resistance to deformation may change depending on the chemical nature of the system. Previously conducted experimental studies allow us to formulate the requirements for the stand in detail, which enables investigation of the properties of petroleum-based liquids. Thus, it is possible to achieve increased anti-wear properties of petroleum-based liquids when the liquid passes through the gap between the electrodes in an electrostatic field. The voltage between the electrodes should be U = 1000–1500 V, and the speed of the liquid movement in the space between the electrodes should be V = 4.5–6.5 m/s. The power supply unit of the stand for electroprocessing petroleum-based liquids, proposed in this paper, meets these requirements. The article proposes a fundamentally new scheme for the power supply unit of the laboratory stand for direct current electrotreatment of petroleum-based liquids. The power supply unit is a bipolar source of adjustable direct current. It provides smooth regulation of the voltage from 0 to 3000 V and step regulation of the output current. The block has double protection against short circuits at the output and input. Keywords: anti-wear property, oil, influence of an electrostatic field on the anti-wear properties of oil, device for electrostatic treatment of oil.