Application and Future Challenges of Functional Nanocarbon Hybrids

Hybridizing nanocarbons, such as carbon nanotubes (CNTs) or graphene, with an active material is a powerful strategy towards designing next‐generation functional materials for environmental and sustainable energy applications. While research on nanocomposites, created by dispersing the nanocarbon into polymer or ceramic matrices, began almost immediately after the popularization of CNTs and graphene in 1991 and 2004, respectively, nanocarbon hybrids are a relatively recent addition to the family of composite materials. In contrast to nanocomposites, which typically combine the intrinsic properties of both compounds, nanocarbon hybrids additionally provide access to both a large surface area required for gas/liquid‐solid interactions and an extended interface, through which charge and energy transfer processes create synergistic effects that result in unique properties and superior performance. This progress report looks at the history of research on nanocarbons (fullerenes, CNTs and graphene) and their composites and hybrids, presents the origin of synergistic effects, reviews the most intriguing results on nanocarbon hybrid performance in heterogeneous catalysis, electrocatalysis, photocatalysis, batteries, supercapacitors, photovoltaics and sensors, and discusses remaining challenges and future research directions.     

Carbon Cage Vibrations of M@C82 and M2@C2 n (M = La,Ce; 2n = 72, 78, 80): The Role of the Metal Atoms

Infrared spectra of La₂@C₈₀ and a series of Ce-based endohedral metallofullerenes (EMFs), including Ce@C₈₂, Ce₂@C₇₂, Ce₂@C₇₈, and Ce₂@C₈₀ are reported. DFT calculations are used for their thorough analysis and assignment. The vibrations of the fullerene cages in all studied EMFs differ from those of their empty, charged cage analogues. Furthermore, EMFs with the same carbon cage but different type of encapsulated species also show significant differences in their cage vibrational patterns. These phenomena are explained by a different coupling of the vibrational modes as well as by the different charge distributions in EMFs and empty, isostructural fullerene anions.     

Poisson–Nernst–Planck model for an ionic transistor based on a semiconductor membrane

In this paper we developed a Poisson–Nernst–Planck model of an ionic current flowing through a nanopore in a layered solid-state membrane made of a single highly-doped \(n\) -Si layer sandwiched between two thick oxide layers which we call the ionic transistor. We studied this layered membrane for a range of source-drain voltages while keeping the gate (the semiconductor membrane) voltage fixed at a certain value, which was later varied too. We find that for this ionic transistor to be effective in controling the ion fluxes through the nanopore, the gate voltage must be kept relatively large. Another solution could be to increase the surface negative charge on the membrane or to replace the outer oxide layers with the semiconductor material, such as the \(p\) -Si material. The developed model can be applied to study ionic filtering and separation properties of membranes of different composition and nanopore geometries.     

Compacted Modified Propellant Blocks as Traveling Charge in the Hybrid Shot Scheme

The burning of compacted modified propellant charges applied as a traveling charge in the hybrid shot scheme was studied. The block charges were manufactured by pressing fine propellant grains coated by a thin film of polyvinyl butyral. A stick from several pressed pellets was insulated over its lateral surface by a thin layer of silicon paste, glued to the back of the projectile and inserted into the barrel of the 23‐mm smooth‐bore laboratory gun. The loose‐packed accelerator charge was placed in the breech. Combustion was initiated by an igniter plug placed between the traveling and breech charges. A set of piezo‐quartz gauges placed in the breech and along the barrel, as well as a frame‐target device were used for recording characteristics of the firings. It is shown that blocks of this type, applied as the traveling charge, provide a stable burning process resulting in high ballistic performance. The block traveling charge preserves its integrity in the course of its motion along the barrel, and burning envelopes its total mass when pressure in the breach passes the maximum value. The descending portion of the pressure diagram demonstrates appreciable transformation, with convex or secondary hump sections. The shape of spatial pressure profiles behind the moving projectile is also transformed, and the pressure at the projectile butt end may be higher than the pressure in the breech. Compared to the conventional charges at the same maximum pressures the muzzle velocity increment attains 340 m s⁻¹ (or 23 %) for a light 35‐g projectile and 200 m s⁻¹ (or 19 %) for a heavy 104‐g projectile.     

Study of reasons of increased active force using coolant with uncut chip thickness

The use of coolant usually leads to a decrease in active force. However, it is well known that when cutting with small uncut chip thickness while using a coolant, the active force may be greater than when cutting without a coolant. For this reason, finish turning with very small uncut chip thickness and manual scraping is carried out without a coolant. The current explanation of this phenomenon is that the coolant increases the plowing force. The aim of this research is to study the impact of the coolant on the plowing force and to explain the reasons for the increase in active force at small uncut chip thickness. In the chipping process, a new reason was found that explains the increase in the active force when using coolant. It was established that the coolant prevents the buildup. Due to this phenomenon, cutting is performed with the radius of the cutting tool at a negative rake angle and with greater active force than when cutting without a coolant. When cutting without a coolant, a buildup is formed on the radius of the cutting tool; the geometry of the cutting part is improved. This is the real reason for decrease in active force when cutting without a coolant. When using the method of extrapolation on a zero uncut chip thickness under the same conditions without buildup, it was found that using a coolant does not increase, but decrease the plowing force.     

Mass media campaigns within reach: effective efforts with limited resources in Russia's capital city

Mass media campaigns, while often expensive, are proven, cost-effective interventions and should not be considered out-of-reach, especially where governments have some sway over media markets, where large media discounts are possible or where other novel strategies can be employed.     

Structural characterization of β-propiolactone inactivated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) particles

The severe COVID-19 pandemic drives the research toward the SARS-CoV-2 virion structure and the possible therapies against it. Here, we characterized the β-propiolactone inactivated SARS-CoV-2 virions using transmission electron microscopy (TEM) and atomic force microscopy (AFM). We compared the SARS-CoV-2 samples purified by two consecutive chromatographic procedures (size exclusion chromatography [SEC], followed by ion-exchange chromatography [IEC]) with samples purified by ultracentrifugation. The samples prepared using SEC and IEC retained more spikes on the surface than the ones prepared using ultracentrifugation, as confirmed by TEM and AFM. TEM showed that the spike (S) proteins were in the pre-fusion conformation. Notably, the S proteins could be recognized by specific monoclonal antibodies. Analytical TEM showed that the inactivated virions retained nucleic acid. Altogether, we demonstrated that the inactivated SARS-CoV-2 virions retain the structural features of native viruses and provide a prospective vaccine candidate.     

Trends in Chemometrics: Food Authentication,Microbiology, and Effects of Processing

In the last decade, the use of multivariate statistical techniques developed for analytical chemistry has been adopted widely in food science and technology. Usually, chemometrics is applied when there is a large and complex dataset, in terms of sample numbers, types, and responses. The results are used for authentication of geographical origin, farming systems, or even to trace adulteration of high value‐added commodities. In this article, we provide an extensive practical and pragmatic overview on the use of the main chemometrics tools in food science studies, focusing on the effects of process variables on chemical composition and on the authentication of foods based on chemical markers. Pattern recognition methods, such as principal component analysis and cluster analysis, have been used to associate the level of bioactive components with in vitro functional properties, although supervised multivariate statistical methods have been used for authentication purposes. Overall, chemometrics is a useful aid when extensive, multiple, and complex real‐life problems need to be addressed in a multifactorial and holistic context. Undoubtedly, chemometrics should be used by governmental bodies and industries that need to monitor the quality of foods, raw materials, and processes when high‐dimensional data are available. We have focused on practical examples and listed the pros and cons of the most used chemometric tools to help the user choose the most appropriate statistical approach for analysis of complex and multivariate data.     

Modulation of Aptamer–Ligand-Binding by Complementary Oligonucleotides: A G-Quadruplex Anti-Ochratoxin A Aptamer Case Study

Short oligonucleotides are widely used for the construction of aptamer-based sensors and logical bioelements to modulate aptamer–ligand binding. However, relationships between the parameters (length, location of the complementary region) of oligonucleotides and their influence on aptamer–ligand interactions remain unclear. Here, we addressed this task by comparing the effects of short complementary oligonucleotides (ssDNAs) on the structure and ligand-binding ability of an aptamer and identifying ssDNAs’ features that determine these effects. Within this, the interactions between the OTA-specific G-quadruplex aptamer 1.12.2 (5′-GATCGGGTGTGGGTGGCGTAAAGGGA GCATCGGACA-3′) and 21 single-stranded DNA (ssDNA) oligonucleotides complementary to different regions of the aptamer were studied. Two sets of aptamer–ssDNA dissociation constants were obtained in the absence and in the presence of OTA by isothermal calorimetry and fluorescence anisotropy, respectively. In both sets, the binding constants depend on the number of hydrogen bonds formed in the aptamer–ssDNA complex. The ssDNAs’ having more than 23 hydrogen bonds with the aptamer have a lower aptamer dissociation constant than for aptamer–OTA interactions. The ssDNAs’ having less than 18 hydrogen bonds did not affect the aptamer–OTA affinity. The location of ssDNA’s complementary site in the aptamer affeced the kinetics of the interaction and retention of OTA-binding in aptamer–ssDNA complexes. The location of the ssDNA site in the aptamer G-quadruplex led to its unfolding. In the presence of OTA, the unfolding process was longer and takes from 20 to 70 min. The refolding in the presence of OTA was possible and depends on the length and location of the ssDNA’s complementary site. The location of the ssDNA site in the tail region led to its rapid displacement and wasn’t affecting the G-qaudruplex’s integrity. It makes the tail region more perspective for the development of ssDNA-based tools using this aptamer.