Surface Area Research Articles

Revealing the Role of the Arg and Lys in Shifting Paradigm from BTK Selective inhibition to the BTK/HCK Dual inhibition- Delving into the Inhibitory Activity of KIN-8194 Against BTK, and HCK in the Treatment of Mutated 〖BTK〗^Cys481 Waldenström Macroglobulinemia: A computational Approach.

Despite the early success of Bruton's tyrosine kinase (BTK) inhibitors in the treatment of Waldenström macroglobulinemia (WM), these single-target drug therapies have limitations in their clinical applications, such as drug resistance. Several alternative strategies have been developed, including the use of dual inhibitors, to maximize the therapeutic potential of these drugs. Recently, the pharmacological activity of KIN-8194 was repurposed to serve as a 'dual-target' inhibitor of BTK and Hematopoietic Cell Kinase (HCK). However, the structural dual inhibitory mechanism remains unexplored, hence the aim of this study. Conducting predictive pharmacokinetic profiling of KIN-8194, as well as demonstrating a comparative structural mechanism of inhibition against the above-mentioned enzymes. Our results revealed favourable binding affinities of -20.17 kcal/mol, and -35.82 kcal/mol for KIN-8194 towards HCK and BTK, respectively. Catalytic residues Arg137/174 and Lys42/170 in BTK and Arg303 and Lys75/173/244/247 in HCK were identified as crucial mediators of the dual binding mechanism of KIN-8194, corroborated by high per-residue energy contributions and consistent high-affinity interactions of these residues. Prediction of the pharmacokinetics and physicochemical properties of KIN-8194 further established its inhibitory potential, evidenced by the favourable absorption, metabolism, excretion, and minimal toxicity properties. Structurally, KIN-8194 impacted the stability, flexibility, solvent-accessible surface area, and rigidity of BTK and HCK, characterized by various alterations observed in the bound and unbound structures, which proved enough to disrupt their biological function. These structural insights provided a baseline for the understanding of the dual inhibitory activity of KIN-8194. Establishing the cruciality of the interactions between the KIN-8194 and Arg and Lys residues could guide the structure-based design of novel dual BTK/HCK inhibitors with improved therapeutic activities.

Multisolid waste collaborative production of aeolian sand-red mud-fly ash cemented paste backfill

This study proposed the novel idea of anaolian sand-red mud-fly ash cemented paste backfill (ARFCPB) to realize low-carbon backfill mining. This idea realizes large-scale disposal and resource utilization of red mud (RM) and fly ash (FA) solid wastes. The influence of the FA/RM mass ratio and mass concentration on the mechanism of action of ARFCPB was explored through comprehensive rheological performance, mechanical property, microscopic, and leaching toxicity tests. The results showed that the fresh ARFCPB slurry could be described by the Herschel–Bulkley model (R2 ≥ 0.964). As the FA/RM mass ratio increased, the ARFCPB slurry yield stress decreased, the thixotropy decreased, and the slump increased. This is because RM has a large specific surface area and an unsmooth surface, resulting in greater water absorption by RM than by FA. In addition, the uniaxial compressive strength (UCS) of ARFCPB can meet the needs of backfill mining with higher strength requirements. UCS first increases and then decreases with increasing FA/RM mass ratio, which is optimal when the mass ratio of FA to RM is 4. When the FA/RM mass ratio was 4, the UCSs of specimens A4 and B4 with mass concentrations of 78% and 80%, respectively, were 5.6MPa and 6.4MPa after 28 days of curing. The leaching results of heavy metal ions in group B4 meet the Class III groundwater standards and can be used for centralized drinking water sources and industrial and agricultural water. Considering the fluidity characteristics, mechanical properties, and leaching results, B4 was identified as the optimal formulation. Finally, the microstructure of the ARFCPB was studied using ultrasonic pulse velocity (UPV) and SEM. The results can contribute to clean production in the aluminum production industry, coal-fired power plants, and coal mines.

Optimization of Energy Consumption in Formaldehyde Production Process Using Reboiled Absorption Process

Formaldehyde is a crucial chemical building block in various industries, and its production often involves energy-intensive processes. This study focuses on optimizing energy consumption in formaldehyde production, explicitly employing the reboiled absorption process with a production capacity of 27,000 tons per year. The objective of this article is to develop a more energy-efficient process of formaldehyde synthesis by addition or refrigerant cycle stream to preserve the energy, reducing energy consumption and improving the sustainability of the process. The reboiled absorption process involves the absorption of formaldehyde gas into a liquid absorbent, followed by reboiling to release the absorbed formaldehyde. A comprehensive analysis of the entire production system compares unmodified and modified process simulations, heat integration, and energy analysis. Beside the energy consumption of the process, the number of stages within the absorption process contributes to the product mass flow rate of the overall process by increasing the surface area which mass transfer can occur. However, adding too many stages to the process may negatively impact the energy efficiency of the process. Therefore, optimizing energy consumption and absorption processes in formaldehyde production is essential to improve the sustainability of the process and increase the overall profitability of the production process. The results show that the proposed method dramatically improves the sustainability of CH2O synthesis by reducing overall energy consumption and emissions by 93.978%, reducing energy consumption from 153,735,360.4 kJ/h to 9,256,646.618 kJ/h. Copyright © 2024 by Authors, Published by Universitas Diponegoro and BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

3D Mitochondrial Structure in Aging Human Skeletal Muscle: Insights into MFN-2 Mediated Changes.

Age-related atrophy of skeletal muscle, is characterized by loss of mass, strength, endurance, and oxidative capacity during aging. Notably, bioenergetics and protein turnover studies have shown that mitochondria mediate this decline in function. Although exercise has been the only therapy to mitigate sarcopenia, the mechanisms that govern how exercise serves to promote healthy muscle aging are unclear. Mitochondrial aging is associated with decreased mitochondrial capacity, so we sought to investigate how aging affects mitochondrial structure and potential age-related regulators. Specifically, the three-dimensional (3D) mitochondrial structure associated with morphological changes in skeletal muscle during aging requires further elucidation. We hypothesized that aging causes structural remodeling of mitochondrial 3D architecture representative of dysfunction, and this effect is mitigated by exercise. We used serial block-face scanning electron microscopy to image human skeletal tissue samples, followed by manual contour tracing using Amira software for 3D reconstruction and subsequent analysis of mitochondria. We then applied a rigorous in vitro and in vivo exercise regimen during aging. Across 5 human cohorts, we correlate differences in magnetic resonance imaging, mitochondria 3D structure, exercise parameters, and plasma immune markers between young (under 50 years) and old (over 50 years) individuals. We found that mitochondria we less spherical and more complex, indicating age-related declines in contact site capacity. Additionally, aged samples showed a larger volume phenotype in both female and male humans, indicating potential mitochondrial swelling. Concomitantly, muscle area, exercise capacity, and mitochondrial dynamic proteins showed age-related losses. Exercise stimulation restored mitofusin 2 (MFN2), one such of these mitochondrial dynamic proteins, which we show is required for the integrity of mitochondrial structure. Furthermore, we show that this pathway is evolutionarily conserved as Marf, the MFN2 ortholog in Drosophila, knockdown alters mitochondrial morphology and leads to the downregulation of genes regulating mitochondrial processes. Our results define age-related structural changes in mitochondria and further suggest that exercise may mitigate age-related structural decline through modulation of mitofusin 2.

Age-related changes in the endocranial capacity and surface area of ancient children from the Zaghunluq Cemetery (650-150 BCE) in Xinjiang, Northwestern China.

Early childhood is an important period for the rapid growth of the brain, which is crucial to neural connection and cognitive development. The purpose of this study is to characterize the age changes of endocasts in ancient children in Northwestern China (2600-2100 BP) to enrich our understanding of brain growth. 28 crania of ancient children excavated from the Zaghunluq cemetery were analyzed using endocasts generated from CT images. The endocast features of age-related changes were assessed by comparing the endocranial volume (cranial capacity), the intracranial surface area, and their ratios among different age groups: 2, 3-5, 6-7, 8-10, 12-15, and 17-19 years. The results demonstrated that with the increase of age, the volume and the surface area of children's endocasts seem to increase between age groups. The growth spurt periods of endocranial volume are 3-5 years old and 8-10 years old, and the growth spurt period of endocranial surface area is 3-5 years old, similar to the patterns in modern children. The increase of endocast surface area is smaller than that of volume, resulting in an overall increase in the ratio of endocranial volume to surface area, indicating a trend of gradual globularization of the brain.

Influence of hydraulic pressure on pore structure evolution and chloride transport in concrete

To study the influence of hydraulic pressure on pore structure evolution and chloride transport behaviour in concrete, the mass transport depth, chloride concentration and pore characteristics of specimens with different water/cement (w/c) ratios were investigated using silver nitrate spraying, potentiometric titration, mercury intrusion porosimetry, nitrogen adsorption tests and confocal laser scanning microscopy. The results showed that the chloride concentration increased with increases in the hydraulic pressure and w/c ratio. With increasing hydraulic pressure, the transport depths of water and chloride ion transport expanded from 5.2 mm to 25.4 mm. An increase in hydraulic pressure changed the pore structure of the concrete, leading to a surge in the specific surface area, greater porosity and larger average pore diameters. Notably, ink-bottle shaped pores emerged prominently and the proportion of fine mesopores and capillary pores markedly increased after the application of hydraulic pressure. A relationship between the chloride diffusion coefficient and hydraulic pressure was developed and a relationship between the modified permeability coefficient and hydraulic pressure was constructed based on the mesoporous contribution to express the hysteresis effect of chloride.

Trojan Microparticles : A Composite Nanoparticle Delivery System

Abstract: In recent years, microparticulate systems have drawn growing attention as a viable strategy for delivering cells, proteins, and medications to target areas. The Nanoparticles-in-Microparticles System (NiMS) is a drug delivery method that combines nano- and microparticles to deliver medications or genes to particular bodily regions with precision. A promising method for achieving dual or multiple functions inside a formulation is the development of nanoparticle-in-microparticle systems (NiMS). NiMS comprises a microparticle (M.P.) matrix and one or more nanoparticles (N.P.s). The N.P.s can be designed to provide specific functionality, such as targeted drug delivery or imaging, while the M.P. matrix can be tailored to provide sustained release or protect the N.P.s from degradation. NiMS offer several advantages over traditional formulations, including the ability to control release profiles and achieve site-specific delivery. By combining different types of N.P.s and M.P.s, it is possible to create formulations that release drugs at different rates or with different kinetics, allowing for tailored treatment regimens. Additionally, by lowering off-target effects and boosting efficacy, the site-specific targeting offered by NiMS can enhance the therapeutic index of medications. Microparticles are small, micron-sized particles that can be loaded with therapeutic agents and designed to deliver them to specific tissues in the body. The pharmaceutical sector is developing microparticulate delivery systems for oral, pulmonary, and cutaneous administration. For instance, a promising strategy for treating respiratory conditions, including asthma and chronic obstructive pulmonary disease, is the development of inhalable microparticles (COPD). Moreover, the use of microparticles for topical drug delivery is being studied, where they can be formulated into creams, gels, or patches for treating skin disorders. The composition of microparticles is crucial for successful tissue regeneration because the particles must be biocompatible and able to interact with the cells in the targeted tissue. In addition, the size and shape of the particles can affect their behavior and how they interact with cells. Chemical and biological sensors and devices, optical detectors, electronic components, and nanoscale production depend on nanostructures because they offer unique properties, such as increased surface area and enhanced reactivity, which can be exploited to create more efficient and effective devices.

Two-dimensional MXene Nanomaterials: Preparation, Structure Modulation and the Applications in Electrochemical Energy Storage.

MXenes have attracted intensive attention owing to their unique twodimensional (2D) layered structure, high specific surface area, excellent conductivity, superior surface hydrophilicity, and chemical stability. In recent years, selective etching of the A element layers from MAX phases by fluorine-containing etchants (HF, LiF-HCl, etc) is a common method to prepare multilayered MXene nanomaterials (NMs) with plentiful surface terminations. At present, many studies have been reported on the use of fluorine-free etchants (NaOH, ZnCl2, etc) to etch MAX phases. The properties of MXene NMs are dependent on their structures. The purpose of this review is to focus on a comprehensive and systematical survey on the preparation, structure modulation, and applications of MXene NMs in electrochemical energy storage devices, including supercapacitors, lithium-ion battery, sodium-ion battery, potassium-ion battery, and aluminum-ion battery. Extensive information related to the preparation and applications of 2D MXene NMs for electrochemical energy storage and their associated patents were collected. This review highlights the recently reported 2D MXene NMs which are used in supercapacitor and various metal ion. It is found that the preparation methods have great impacts on the layer spacing and surface terminations of MXenes, consequently affecting their performance. Hence, this paper summarizes the research progress of the preparation strategies, layer spacing and surface termination modulation of MXene NMs. The applications of 2D MXene NMs in electrochemical energy storage are outlined. The forward-looking challenges and prospects for the development of MXenes are also proposed.

Electrosynthesis of a triazole derivative on the glassy carbon surface for the electrochemical determination of catechol

ABSTRACT In this experiment, an electrosynthesis of a triazole-thiol derivative (3-amino-1,2,4-triazole-5-thiol (3ATT)) was carried out on the glassy carbon electrode (GCE) to fabricate an electrochemical sensor to determine catechol (CC) by voltammetry. The characterisation of the modified electrode (3ATT-GCE) was examined by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). Electrochemical oxidation of CC by the differential pulse voltammetry (DPV) with 3ATT-GCE exhibited a perfectly wide linear response in the CC concentration range of 0.088 to 10.5 µM and 10.5 to 629 µM with a detection limit (LOD) of 0.024 µM (3 s/m). Furthermore, it indicated excellent reproducibility and repeatability. The fabricated sensor with a large surface area and high electrical conductivity was successfully employed to determine CC in tap water without being affected by interfering substances.

Tailoring Ti3C2Tx MXene Flake Sizes for Modified Electrochemical Performance: A Top-down Approach

Introduction: Two-dimensional (2D) materials, such as MXene (Ti3C2Tx), have garnered extensive attention in recent years due to their exceptional performance across various domains. The flake size of Ti3C2Tx notably influences its specific surface area, a pivotal factor in interfacial interactions within electrochemistry. Method: Presently, modifying the flake size of bulk Ti3C2Tx typically involves complex and costly processes, like ultrasonic treatment and isolation. Leveraging the specific preparation principle of MXenes, which involves etching the A layers in precursor MAX phases, a topdown strategy for producing Ti3C2Tx flakes of desired sizes, has been proposed in this work. In this approach, precursor Ti3AlC2 particles undergo ball-milling to adjust their size. Result: Through this innovative strategy, dispersions of Ti3C2Tx flakes with varying average lateral sizes are generated, enabling an investigation into the impact of lateral size on the electrochemical properties of Ti3C2Tx flakes. By controlling the ball milling time for Ti3AlC2 powders, the resulting average sizes of Ti3C2Tx (0, 2, 4) are 6.34 μm, 2.16 μm, and 0.96 μm, respectively. Particularly, the Ti3C2Tx (2) electrode, composed of 2.16 μm sheets, demonstrates remarkable performance metrics. It exhibits a high areal capacitance of 845.0 mF/cm2 at a scan rate of 5 mV/s, along with a gravimetric capacitance of 244.0 F/g at a current density of 1 A/g. Conclusion: This study presents a facile method to enable mass production of Ti3C2Tx with sheets of varying sizes, addressing both small and large dimensions.

Normal Contact Model of Fractal Surfaces Considering Friction and Asperity Interactions

Friction as well as asperity interactions have significant influence on the contact area and force of rough surfaces. In this work, a single-asperity, elastoplastic contact model, considering friction, is established by means of continuum mechanics and power-exponential functions. Then, the deformation of the asperity interactions is modeled by the displacement of the average line for asperity height. Using fractal theory, the actual deformation and contact stiffness of an asperity are derived, which take the friction and asperity interactions into account. Furthermore, the actual contact area and normal stiffness models for fractal surfaces are developed, accounting for friction and asperity interactions. The accuracy of the developed models is confirmed by using published experimental results. The developed models are closer to experimental results than the reported fractal contact models. Finally, the effects of the friction coefficient and surface morphology parameters on contact characteristics are discussed.

Molecular Mechanism for Regioselectivity of P450-BM3 Monooxygenase Towards Stearic Acid Hydroxylation

Hydroxy stearic acid is an important raw material for the synthesis of biobased materials, and the hydroxylation at different positions showed different properties. With the catalysis of P450-BM3 monooxygenase, (ω - 1)-Hydroxy stearic acid was generated, which is a precursor of macrocyclic musk. Experimental results have shown that the L188Q mutant can increase the yield of (ω - 1)-Hydroxy stearic acid by more than three times, but the reason and underlying molecular mechanism are still unclear. In this study, molecular dynamics (MD) simulations were conducted to study the structural characteristics of the P450-BM3 wild type and its three mutants (F87V, L188Q, and F87V-L188Q) in combination with stearic acid. The MD simulation results showed significant changes in the interactions between the three mutants and the carboxyl- and terminal-end of stearic acid. The results of the Molecular mechanics-Poisson-Boltzmann surface area (MMPBSA) binding free energies indicated that the L188Q mutant showed the most stable binding with the stearic acid. Finally, the H-abstraction free energy barriers of L188Q and wild type systems were calculated to study the regioselectivity, and the results indicated that the L188Q mutant shown a significant advantage in the hydroxylation of stearic acid at the ω - 1 position. Our research results not only explain molecular mechanism for regioselectivity of P450-BM3 towards stearic acid hydroxylation, but also provide some useful ideas for the synthesis of biobased materials from hydroxy fatty acids.

Partial root-zone drying irrigation improves intrinsic water-use efficiency and maintains high photosynthesis by uncoupling stomatal and mesophyll conductance in cotton leaves.

Partial root-zone drying irrigation (PRD) can improve water-use efficiency (WUE) without reductions in photosynthesis; however, the mechanism by which this is attained is unclear. To amend that, PRD conditions were simulated by polyethylene glycol 6000 in a root-splitting system and the effects of PRD on cotton growth were studied. Results showed that PRD decreased stomatal conductance (gs) but increased mesophyll conductance (gm). Due to the contrasting effects on gs and gm, net photosynthetic rate (AN) remained unaffected, while the enhanced gm/gs ratio facilitated a larger intrinsic WUE. Further analyses indicated that PRD-induced reduction of gs was related to decreased stomatal size and stomatal pore area in adaxial and abaxial surface which was ascribed to lower pore length and width. PRD-induced variation of gm was ascribed to the reduced liquid-phase resistance, due to increases in chloroplast area facing to intercellular airspaces and the ratio of chloroplast surface area to total mesophyll cell area exposed to intercellular airspaces, as well as to decreases in the distance between cell wall and chloroplast, and between adjacent chloroplasts. The above results demonstrate that PRD, through alterations to stomatal and mesophyll structures, decoupled gs and gm responses, which ultimately increased intrinsic WUE and maintained AN.

RICH1 is a novel key suppressor of isoproterenol‑ or angiotensin II‑induced cardiomyocyte hypertrophy.

Cardiac hypertrophy is one of the key processes in the development of heart failure. Notably, small GTPases and GTPase‑activating proteins (GAPs) serve essential roles in cardiac hypertrophy. RhoGAP interacting with CIP4 homologs protein 1 (RICH1) is a RhoGAP that can regulate Cdc42/Rac1 and F‑actin dynamics. RICH1 is involved in cell proliferation and adhesion; however, to the best of our knowledge, its role in cardiac hypertrophy remains unknown. In the present study, the role of RICH1 in cardiomyocyte hypertrophy was assessed. Cell viability was analyzed using the Cell Counting Kit‑8 assay and cells surface area (CSA) was determined by cell fluorescence staining. Reverse transcription‑quantitative PCR and western blotting were used to assess the mRNA expression levels of hypertrophic marker genes, such as Nppa, Nppb and Myh7, and the protein expression levels of RICH1, respectively. RICH1 was shown to be downregulated in isoproterenol (ISO)‑ or angiotensin II (Ang II)‑treated H9c2 cells. Notably, overexpression of RICH1 attenuated the upregulation of hypertrophy‑related markers, such as Nppa, Nppb and Myh7, and the enlargement of CSA induced by ISO and Ang II. By contrast, the knockdown of RICH1 exacerbated these effects. These findings suggested that RICH1 may be a novel suppressor of ISO‑ or Ang II‑induced cardiomyocyte hypertrophy. The results of the present study will be beneficial to further studies assessing the role of RICH1 and its downstream molecules in inhibiting cardiac hypertrophy.

Current Expansion of Silver and Gold Nanomaterials towards Cancer Theranostics: Development of Therapeutics

Abstract: Nanomaterial-based therapeutics is an emerging tool for the treatment of numerous types of cancer. Various types of polymeric, lipid and inorganic nanoparticles (NPs) result in a wider series of applications in cancer diagnosis and therapeutics. The NPs properties are due to high surface area to volume ratio, surface plasmon resonance, absorption in the visible spectrum and light scattering. These unique characteristics of NPs arise due to their optical surface properties for conjugation/surface modification and smaller size. In cancer therapeutics, NPs based products are used as a biomarker for early detection/diagnosis of tumours, drug nano-conjugates for the delivery of chemotherapeutic drugs to the tumour-specific site, chemo-protective agents, etc. : Furthermore, other advantages of NPs are biocompatibility, lesser toxicity, enhanced permeability and retention effect, higher stability, and specific targeting with a selective accumulation of nano drugs in the tissue of the tumour. The selective targeting of NPs to tumour tissue is possible by adding surface-active targeting agents i.e., antibodies. The selective transport of drug NPs conjugates to the cancer cells is increased and extravagated due to permeable vasculature from endothelial cells gap while failing the transport of drug NPs conjugates in normal cells. This review emphasizes metallic NPs, including silver NPs (AgNPs) and gold NPs (AuNPs), which are extensively reconnoitered in various applications in cellular targeting, imaging, drug delivery, DNA-NPs conjugates for biosensor/point of care devices development, photothermal/photodynamic therapy, protein-protein interaction, etc. In addition, this review discussed different synthetic methods of AgNPs and AuNPs and characterization methods. Furthermore, it highlighted the different properties and applications of AgNPs and AuNPs in cancer theranostics.

Retentive strength of cement-retained implant-supported fixed dental prostheses according to different cement types and cementation protocols: An in vitro study.

To develop the most compatible cementation protocol for ensuring minimal residual cement and optimal retention of cement-retained implant-supported fixed dental prostheses. Thirty custom implant abutments and zirconia crowns with bilateral wings were prepared. Three cement types were used for cementation: non-eugenol resin cement (Premier Implant Cement; Group IC), dual-polymerizing self-adhesive resin cement (SmartCem 2; Group SC), and zinc oxide eugenol cement (Temp-Bond; Group TB) (n=30 per group). Three cementation methods were applied for each cement type and the samples were divided into subgroups: 1) cement was injected using a graduated syringe (IC-N, SC-N, and TB-N); 2) a cementation jig made with a silicone impression material and temporary resin material was used (IC-CJ, SC-CJ, and TB-CJ); 3) three dimensionally (3D) printed abutments were used as replicas for cementation (IC-3DP, SC-3DP, and TB-3DP). The amount of cement injected, surface area of the residual cement, and retentive strength were measured. Kruskal-Wallis and post-hoc Mann-Whitney tests were used for statistical analyses. Excess cement was not observed when cementation jig or 3D-printed replicas were used. For IC and SC subgroups, non-use of these auxiliary tools resulted in significantly higher amounts of injected cement. The retentive strength differed significantly among the IC subgroups, but not among the SC subgroups. The retentive strength of subgroups TB-N and TB-CJ was significantly higher than that of subgroup TB-3DP. To prolong the main purpose of each cement type, a cementation jig or 3D-printed replica is highly recommended regardless of the cement type. Int J Prosthodont 2023. doi: 10.11607/ijp.8344.

The Effect of Solvent on the Characteristics of FeBTC MOF as a Potential Heterogenous Catalyst Prepared via Green Mechanochemical Process

In this study, the synthesis of FeBTC (BTC = 1,3,5-benzenetricarboxylate) also known as MIL-100 (Fe) metal organic framework (MOF) has been carried out successfully using green mechanochemical method (neat grinding and liquid assisted grinding). The effect of solvent used in the synthesis was investigated for the first time to elucidate the physicochemical properties of FeBTC including crystal structure, thermal stability, pore size and specific surface area. The physicochemical properties of all FeBTC obtained in this study were compared to commercial FeBTC (Basolite F-300), characterized using powder X-Ray Diffraction (XRD), Thermogravimetric Analysis (TGA) and nitrogen physisorption isotherms. All Fe-BTC MOF synthesized in this study showed improved textural properties compared to commercial Basolite F-300 such as higher crystallinity, higher surface area and larger pore size. It was found that the best synthesis method was by using the mixture of ethanol and water with equal volume ratio as solvent. The highest BET surface area of FeBTC synthesized using this method was 972 m2/g for FeBTC-EtOH/H2O. This value is 2.3 times higher than the surface area of commercial Basolite F-300 (418 m2/g). FeBTC with higher surface area is expected to have higher catalytic activity which makes this FeBTC an excellent candidate as a heterogenous catalyst for many reactions such as aldol condensation or esterification reaction. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

The Properties and Activity of TiO2-based Nanorods as an Anti-Fouling Agent and a Photocatalyst

The properties and activity of TiO2-based nanorods as an antifouling agent and a photocatalyst for the catalytic degradation of methylene blue (MB) have been investigated. A modification of TiO2 with SiO2 was first carried out to enlarge the surface area. In order to enhance the TiO­2 photo response to the visible light region, a further modification of TiO2-SiO2 (TS) composites with polyaniline (PANI) was also conducted. The nanorod TiO2 exhibited an anatase structure based on the diffraction patterns. The TEM images showed that some TiO2 molecules were attached around SiO2 with a random orientation. The TiO2-SiO2-PANI (TS-PANI) exhibited the largest specific surface area (SBET) of about 256.85 m2/g. The profile on the AFM images of the composites showed that the nano-roughness of the coatings was confirmed. The photocatalytic activity was evaluated through the decomposition of MB both on the powder and the coated composites. The photocatalytic activity on the coatings was verified due to further application as anti-fouling coatings involving photocatalytic mechanism. The decomposition of MB using TS-PANI powder and TS-PANI coating composites was 89.5% and 90.2 %, respectively, with the irradiation time on the coatings was 20 min longer. The anti-fouling activity through the photocatalytic mechanism and nano-roughness surface was confirmed by the inhibition of barnacle growth on the teakwood surface immersed for two months in the sea.

СТЕКЛОКЕРАМИЧЕСКИЕ ПОКРЫТИЯ НА ДЕНТАЛЬНЫХ ИМПЛАНТАТАХ С БАРЬЕРНЫМИ СВОЙСТВАМИ

Pateks — the technology of applying a biocompatible glass-ceramic coating based on silicon, carbon and nitrogen on dental implants by PECVD is developed by research and production company Plasmacentre and Pavlov University (St. Petersburg, Russia). Purpose of the research — to evaluate the success of optimization of the surface of doped titanium endosseous dental implants which may be achieved with our glass-ceramic barrier coating technology using physicochemical, cytological and spectrophotometric researches. The main task is to carry out a comparative assessment of the studies’ results between dental implants with and without Pateks glass-ceramic coating (doped with titanium alloy). Materials and methods. Titanium implants (grade 5) from BioMed were used in this research. Some of them were coated with Pateks according to our technology. A human lung fibroblast cells culture was used for the cytological study. Spectrophotometric studies were carried out on atomic absorption spectrophotometer and a atomic absorption spectrometer KVANT-Z.ETA (Russia). Findings. Pateks-coated implants demonstrate advantage in comparison with non-coated ones in certain physicochemical parameters such as decrease of defects’ area in the initial surface of titanium implants which is formed on the previous stages of surface shaping and processing, providing higher surface hydrophilicity, increasing of dielectric characteristics and higher pH value. Pateks coating is safe for fibroblast monolayers and does not inhibit respiratory processes in them. Applying of Pateks glass-ceramic coating with a thickness of 0.5 μm reduces the content of aluminum and vanadium ions in the model medium by almost 2 times and pro- vides a barrier that helps to reduce the negative biological effect of these ions on peri-implant tissues.

Catalytic Hydroconversion of Lauric Acid Over Poly(N-vinyl-2-pyrrolidone)-Coated Pd Nanoparticles on ZIF-8

A subclass of Metal-Organic Frameworks, Zeolitic Imidazole Frameworks-8 (ZIF-8) is known as an emerging material that has the characteristic of a large surface area, good thermal stability as well as a high porosity. Instead of having extraordinary properties, ZIF-8 consists of Lewis acid and Lewis base site on its Zn metals and 2-methylimidazole which are the important components for the catalyst. In this study, Pd-Poly(N-vinyl-2-pyrrolidone) coated on ZIF-8 (Pd-PVP@ZIF-8) was synthesized by mixed Pd-PVP solution and ZIF-8 precursors at room temperature. The Pd-PVP solution was varied from 10 to 50 ml to differentiate the Pd concentration in ZIF-8. As-synthesized 50 ml of Pd-PVP on ZIF-8 (50Pd-PVP@ZIF-8) showed catalytic activity in the conversion of 98.6% lauric acid to produce 78.2% of 1-dodecanol at optimum condition 320 °C for 6 h. The synergy between Pd-PVP as metal and ZIF-8 as metal support as well as high dispersion of Pd particles could enhance performance in the conversion of lauric acid. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).