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Magnesium slag (MS) and fly ash (FA) are industrial wastes that must be utilized in a clean, effective, and massive method to avoid environmental pollution. In this study, the preparation of diopside-augite-based glass-ceramics was theoretically analyzed and experimentally conducted by disposal of MS and FA with chromium oxide (Cr 2 O 3) as a nucleating agent. The thermodynamics analysis first indicated that pyroxene could be the main crystal phase of the target glass-ceramics for the co-utilization of both wastes. The experimental results indicated that the main phase in prepared glass-ceramics samples was diopside ([Ca(Mg, Fe, Al)(Si, Al) 2 O 6 ], and the degree of glass network polymerization was enhanced with the FA in raw material increasing from 50 wt% to 65 wt%. Plus, the crystal size of the prepared glass-ceramics was gradually refined by increasing the FA. The optimized conditions were given as controlling nucleation at 790 °C for 2 h and crystallization at 929 °C for 2 h of the parent glass that derived from 40 wt% MS and 60 wt% FA as raw materials, 1 wt% Cr 2 O 3 as nucleating agent. The resulting glass-ceramics had excellent properties and chemical stability, such as a density of 3.11 g cm−3, bending strength of 101.98 MPa, acid resistance of 98.34 %, and alkali resistance of 99.53 %. This study provided a route to produce eco-friendly glass-ceramics material for architectural decoration by high-efficiency utilization of MS and FA. [ABSTRACT FROM AUTHOR]

The effectiveness of treating bacterial infections is seriously jeopardized by the emergence of bacterial resistance to chemical therapy. The development of biofilm in bacteria is one of the main causes of resistance to antimicrobial drugs. By developing new antibiofilm medications, quorum sensing (QS) inhibitor was developed as an alternate therapy. QS inhibition, which focuses on the QS signaling pathway, obstructs cell–cell communication. The aim of this work is to develop newer QS inhibitors against Pseudomonas aeruginosa. N‐(Pyridin‐2/3‐yl)alkanamide derivatives were designed as QS inhibitors, and these designed molecules were synthesized. QS inhibitor activity was evaluated for the synthesized compounds (3a–l, 4a–h). The highest QS inhibitor activities for compounds 3k, 4a, and 4c were 11.66 ± 0.11, 14.66 ± 0.15, and 10.66 ± 0.05 mm, respectively. Subsequent molecular docking analyses exhibited moderate to good binding affinity values between −7.1 and −9.3 kcal/mol. Using the in silico method, the physicochemical characteristics of these prepared compounds were examined. Additionally, molecular dynamic simulation was employed to gain a deeper comprehension of stability of the protein and ligand complexes of compounds 3k, 4a, and 4c. The overall findings of the study indicated that N‐(pyridin‐2/3‐yl)alkanamide derivatives might be significant for the development of newer QS inhibitors. [ABSTRACT FROM AUTHOR]

The synthesis and characterization of poly(vinylidene fluoride) (PVDF)‐based block copolymers using a metal‐free light‐catalyzed atom transfer radical polymerization (ATRP) approach are described. A PVDF macroinitiator with C─Br bonds at both ends of the chain is synthesized, and an organic photoredox catalyst (OPRC) is used to control the process. The metal‐free process expands the possibilities for the synthesis and application of PVDF‐based block copolymers, as it allows the use of monomers that is previously incompatible with classical ATRP due to their interaction with metal catalysts. The synthesized block copolymers are characterized structurally and thermally as powder materials and in thin films. Fourier‐transform infrared spectroscopy (FT‐IR) analysis revealed that the crystalline phase of PVDF changes when thin films are formed. Specifically, the disappearance of the FT‐IR peaks related to the gamma phase and the presence of characteristic peaks related to the alpha and beta phases indicate that film formation rearranged the PVDF chains, leading to changes in their crystalline phases. These PVDF‐based block copolymers have unique properties, including high thermal stability, chemical resistance, and piezoelectricity, making them potential candidates for use in various fields, such as biomedical engineering, energy storage, and electronic devices. [ABSTRACT FROM AUTHOR]

The spread of arboviruses like yellow fever, dengue, chikungunya, and Zika, transmitted by the invasive mosquito Aedes aegypti has led to the development of many strategies to suppress mosquito populations. Given the rapid development of resistance to common chemical larvicides and adulticides in some Ae. aegypti populations, as well as the ever-shrinking chemical options for mosquito control, there is a pressing need for new tools and deployment of those innovative tools as a component of integrative mosquito management programs. Prior to the adoption of any mosquito population intervention, be it conventional or innovative, understanding the baseline population is essential to evaluate the efficacy of the control measure. The Lee County Mosquito Control District in Florida has collected a three-year-long period of baseline entomological surveillance data collection for Ae. aegypti on Captiva and Sanibel Islands as foundational information prior to implementation of a new integrative mosquito management approach. We identified 18 mosquito species and described their population dynamics during the rainy and dry seasons. The two islands had no significant differences in species richness, diversity, dominance, or evenness overall. Yet, there were clear differences between the high rain season and low rain season in the Shannon diversity index, Simpson dominance index, and Pielou species evenness index within each site. Our data suggest that any innovative intervention should begin before mid to late April when the mosquito population is at its lowest and certainly before populations build up to their summer peak between June and September. These data also show the spatial distribution of Ae. aegypti is dynamic in space and time, identifying hotspots of mosquito abundance to focus on for future interventions. Overall, our study emphasizes the importance of entomological data collection to understand the population dynamics of Ae. aegypti mosquitoes, including the impact of environmental factors such as temperature and precipitation. [ABSTRACT FROM AUTHOR]

This research study employs a comparative Multi-Criteria Decision-Making (MCDM) approach to select optimal thermoplastic materials for hybrid vehicle battery packs in the automotive industry, addressing the challenges posed by high-temperature environments. Through a detailed evaluation of materials based on criteria such as thermal stability, mechanical strength, chemical resistance, and environmental impact, the research identifies materials that enhance battery efficiency, longevity, and vehicle performance. Utilizing SWARA-ARAS, SWARA-EDAS, and SWARA-TOPSIS methods, the study systematically assesses and ranks various polymers, providing recommendations that prioritize safety, performance, and sustainability. The findings offer valuable insights for manufacturers in making informed material selection decisions, contributing to the advancement of sustainable automotive technologies. This research not only highlights the importance of material selection in the context of hybrid vehicle battery packs but also sets a foundation for future studies to explore emerging materials and decision-making frameworks, aiming to further enhance the efficiency and sustainability of hybrid vehicles. [ABSTRACT FROM AUTHOR]

Recycling of carbon fiber reinforced composites is important for sustainable development and the circular economy. Despite the use of dynamic chemistry, developing high-strength recyclable CFRPs remains a major challenge due to the mutual exclusivity between the dynamic and mechanical properties of materials. Here, we developed a high-strength recyclable epoxy resin (HREP) based on dynamic dithioacetal covalent adaptive network using diglycidyl ether bisphenol A (DGEBA), pentaerythritol tetra(3-mercapto-propionate) (PETMP), and vanillin epoxy resin (VEPR). At high temperatures, the exchange reaction of thermally activated dithioacetals accelerated the rearrangement of the network, giving it significant reprocessing ability. Moreover, HREP exhibited excellent solvent resistance due to the increased cross-linking density. Using this high-strength recyclable epoxy resin as the matrix and carbon fiber modified with hyperbranched ionic liquids (HBP-AMIM+PF6−) as the reinforcing agent, high performance CFRPs were successfully prepared. The tensile strength, interfacial shear strength (IFSS) and interlaminar shear strength (ILSS) of the optimized formulation (HREP20/CF-HBPPF6) were 1016.1, 70.8 and 76.0 MPa, respectively. In addition, the CFRPs demonstrated excellent solvent and acid/alkali-resistance. The CFRPs could completely degrade within 24 h in DMSO at 140 °C, and the recycled CF still maintained the same tensile strength and ILSS as the original after multiple degradation cycles. [ABSTRACT FROM AUTHOR]

The serious environmental threat caused by petroleum-based plastics has spurred more researches in developing substitutes from renewable sources. Starch is desirable for fabricating bioplastic due to its abundance and renewable nature. However, limitations such as brittleness, hydrophilicity, and thermal properties restrict its widespread application. To overcome these issues, covalent adaptable network was constructed to fabricate a fully bio-based starch plastic with multiple advantages via Schiff base reactions. This strategy endowed starch plastic with excellent thermal processability, as evidenced by a low glass transition temperature (Tg = 20.15 °C). Through introducing Priamine with long carbon chains, the starch plastic demonstrated superior flexibility (elongation at break = 45.2%) and waterproof capability (water contact angle = 109.2°). Besides, it possessed a good thermal stability and self-adaptability, as well as solvent resistance and chemical degradability. This work provides a promising method to fabricate fully bio-based plastics as alternative to petroleum-based plastics. [ABSTRACT FROM AUTHOR]

Innovative materials enable two‐photon polymerization for precise additive fabrication of intricate optical components. Existing polymeric inks suffer from poor optical performance due to their high organic content. Silica‐rich sol‐gel ink (75 wt%, under ambient conditions) is presented for high‐precision three‐dimensional (3D) printing of microscale structures and optical devices. A photoinitiator with high‐efficiency nonlinear absorption is introduced to initiate two‐photon polymerization. Utilizing a commercial direct laser writing system, 3D‐printing is demonstrated including the optimization of printing parameters and ink characterization. The optical performance of the printed microscale elements using the new sol‐gel ink surpasses commercially available polymeric inks on key metrics: Printed elements exhibit extremely low surface roughness, 3nm; visible and near‐IR light transmission is greater than 90%; Printed elements present enhanced mechanical and chemical resistance to common organic solvents; Structures exhibit low isotropic shrinkage, <10%; Elements withstand continuous‐wave laser intensities exceeding 7 × 105 W cm−2. Direct writing onto an optical fiber tip with no need for surface functionalization is presented, with the demonstration of a tall waveguide taper (≈1:5 aspect ratio) with low losses and modal crosstalk, and a freestanding photonic lantern mode multiplexer. The new ink can be utilized in a variety of applications and across many materials, requiring compact, durable, and complex optical elements. [ABSTRACT FROM AUTHOR]

Magnesium alloys have a huge market and broad prospects due to their high specific strength, good ductility, and strong thermal conductivity. However, the active chemical properties of elemental magnesium and the negative standard electrode potential result in magnesium alloys being highly susceptible to corrosion and failure. Chemical conversion treatment of magnesium alloy can improve its corrosion resistance by preparing a chemical conversion film on its surface. Rare earth conversion treatment has the advantages of effortless process, moderate price, no pollution, good corrosion resistance, and synergistic effect with inorganic or organic additives, which is in line with the pursuit of “green chemical” in industrial production. At present, there is little research and application on lanthanum-based rare earth conversion coatings (La-RECC). This paper selects rare earth element lanthanum (La) to prepare La-RECC on the surface of AZ91D magnesium alloy through chemical conversion treatment. The microstructure, chemical composition, and protective properties of La-RECC were discovered, as well as their interrelationships, revealing the degradation process of La-RECC in 3.5% NaCl solution. La-RECC is composed of La(OH)3 and Mg(OH)2, exhibiting a crystal cluster structure with cracks, and there are a large number of needle-like crystals on the crystal cluster of La-RECC, with a thickness of 2.14 μm. The degradation process of La-RECC can be divided into three stages: Rapid degradation, slow degradation, and complete degradation. The complete degradation time of La-RECC in 3.5% NaCl solution is 82.5h. [ABSTRACT FROM AUTHOR]

AbstractPolyetheretherketone (PEEK) is a lightweight, bioinert, high-performance thermoplastic that is beginning to see clinical use in orthopedic applications. PEEK outperforms conventional metallic counterparts in terms of reduced stress shielding and improved chemical resistance, making it highly suitable for implantable applications. However, despite its excellent mechanical properties, the elevated melting point (343 °C) presents significant challenges during manufacturing. Furthermore, PEEK requires surface modifications to enhance antibacterial, bioactive, and osseointegration properties suitable for in vivo applications. In this context, the present manuscript highlights current manufacturing challenges for implantable PEEK biomaterials and typical fiber reinforced PEEK composites. Emphasis is placed on reinforcements such as carbon fiber (CF), hydroxyapatite (HA) and titanium dioxide (TiO2), along with multi-material PEEK composites and their applications. Opportunities are identified to address these challenges, contributing toward the development of synergetic, multi-functional PEEK biomaterials suitable for long-term implantable applications. [ABSTRACT FROM AUTHOR]

By combining mechanical treatment of aluminium alloy with subsequent surface modification using micro-arc oxidation (MAO) technology, zinc oxide (ZnO) oxide coatings were prepared, which achieved enhanced hydrophobic properties, excellent antibacterial activity and corrosion resistance. The coatings were oxidised at different MAO discharge intensities using different frequencies. All surfaces were subjected to determination of wettability, corrosion resistance and chemical stability at 1, 7, 14, and 28 days and antibacterial activity of the coatings against the bacterial population of Staphylococcus aureus, Escherichia coli with an evaluation of population inhibition after 24 h. The surfaces mechanically modified by blasting showed a hydrophobic character; their subsequent oxidation by MAO contributed to a significant increase in hydrophobic properties. The sample with the highest Zn content (1.1 wt%), prepared at an MAO source frequency of 222 Hz, i.e. at the most intense plasma discharge, showed the most significant chemical stability in simulated body fluid (SBF) and distilled water and showed the highest antibacterial activity after 24 h. Thus, blasting of aluminium alloy surfaces and their subsequent MAO in alkaline electrolyte allows to obtain oxide coatings with antibacterial, hydrophobic and corrosion-resistant properties with the possibility of their use on surfaces with potential occurrence of harmful bacteria. • Oxide layers on aluminium alloy were prepared in alkaline electrolyte. • Frequencies of 49, 95 and 222 Hz, blasting and MAO technology combination were used. • Mechanically modified layers and MAO coatings achieved hydrophobic properties. • ZnO-doped MAO coatings had antibacterial properties and higher corrosion resistance. [ABSTRACT FROM AUTHOR]

Engineering new chalcogenide solids improves the desired functionality of the materials and may open the way for new applications. Here we discuss the preparation of As x S 100−x amorphous thin films modified with WS 3 by the sol–gel method. We show that the formation of homogeneous, transparent, and stable n-propylamine-based solutions by mixing 0.02M As x S 100−x and 0.02M (NH 4) 2 WS 4 solutions is feasible for the As content in the chalcogenide glass precursor x ≤ 25 at.%. Above this limit, rapid and massive precipitation occurs in the solutions. We further demonstrate the preparation of amorphous thin films along the pseudo-binary AsS 3 - WS 3 tie-line and provide information about the role of WS 3 on optical properties and the structure of tungsten-based chalcogenide thin films. Due to a significant etching contrast between annealed AsS 3 − WS 3 thin films at 70 and 240 ∘ C , we propose tungsten-based chalcogenide thin films as a suitable platform for application in wet-lithography. [Display omitted] • Homogeneous, transparent, and stable solutions by mixing As x S 100−x and (NH 4) 2 WS 4 solutions for x ≤ 25 at.%. • The WS 3 content increases the thermal stability of prepared thin films. • Optically transparent amorphous AsS 3 − WS 3 thin films up to a molar ratio of 1:3. • As WS 3 increases, the absorption edge is red-shifted. • The chemical resistance decreases to amine-based solutions with increasing WS 3 content. [ABSTRACT FROM AUTHOR]

A durable and efficient hydrophobic/superoleophilic MIL-88A(Fe)@sponge (MS) with high throughput was fabricated via the dip-coating technique. Its adsorption capacities for pump oil, peanut oil, and CCl4 were 32.13 g g−1, 34.85 g g−1, and 34.25 g g−1, respectively. The hydrophobic surface of MS has excellent chemical resistance and physical stability in harsh environments. [ABSTRACT FROM AUTHOR]

The demanding and rigorous modern work environments present significant challenges to the protective capabilities of engineering materials. Polyurea elastomers often face limitations in terms of inadequate strength and a lack of weather resistance, however, polyurea composites holds great promise in addressing these issues. This study prepared modified ultrafine aramid short fibers using a mechanochemical method. Subsequently, in‐situ polymerization was utilized to combine the modified ultrafine aramid short fibers (M‐AF) with polyurea, resulting in the synthesis of a composite material characterized by recyclability, robust weather resistance, and favorable mechanical properties. Subsequently, intensive researches were conducted on the mechanical properties, recyclability, self‐healing performance, weather resistance, and chemical medium resistance of the composites. The composite at 0.1 wt% of M‐AF exhibited improvements in tensile strength (27.2 ± 0.8 MPa) as well as obviously enhanced impact performance (428.8 ± 6 kJ/m2), and recovered most of its mechanical properties after recycling and self‐healing. Moreover, the composite exhibits excellent weather resistance and chemical resistance, enabling it to uphold its exceptional protective performance even in the face of challenging environments. Highlights: Ultrafine aramid fibers were prepared using a simple mechanochemical method.Mechanochemical methods were employed to surface modify aramid fibers.The composites have good strength, recyclability, weather resistance. [ABSTRACT FROM AUTHOR]

The aim of this study is to evaluate the potential use of wood ash as a cement additive. Four wood specimens from Yaoundé city of (Cameroon) were used namely: Sapelli, Iroko, Movingui and Padouk. Five mortar were produced, with cement substitutions of 0%, 5%, 10%, 15% and 20%. The fresh rheological, mechanical and hardened durability properties of various mortar were obtained after 7, 14, 28 and 56 days. The results showed that cement paste consistency and the cuing time increases with the addition of ash. At 28 days, the mortars obtained from the 5% and 15% Padouk and Movingui ash substitutes, respectively, showed optimum compressive strength (9%, 6%) and flexural strength (5%, 3%) compared with the control mortar. Due to continuous pozzolanic activity, this flexural gain is multiplied by 3 for Movingui mortar (9%) at 56 days. Compared with the 28-day and 56-day compressive strength results, there were increases of 5% and 4% respectively for the 5% and 15% ash substitutions in Padouk and Movingui mortars. Durability results were evaluated through absorption, which showed relatively identical rates in mortars containing ash from Padouk and Movingui wood, due to their water content for normal consistency. Chemical attack with H2SO2 and NaCl proved that the incorporation of ash improved the mortars' resistance to chemical attack. Thermal analyses and microscopic observations were performed with the optimum. [ABSTRACT FROM AUTHOR]

Shear‐thickening fluids (STFs) undergo significant transformation under shear, transitioning from liquid‐like to solid‐like states, opening up diverse applications. This review comprehensively analyzes recent advances in nanoparticle‐reinforced STFs and highlights their improved rheological and mechanical properties. We explore various STF types, including colloidal suspensions and polymer‐based systems, and investigate the underlying shear‐thickening mechanisms such as order‐disorder, hydrocluster, and contact rheology theories. Nanoparticle reinforcement significantly improves STF performance. In our review, nanoparticle types, incorporation methods, and their effects on STF behavior are systematically investigated. Key results demonstrate significant improvements in stiffness, toughness, thermal stability, and chemical resistance, which are critical for practical applications in protection and smart body armor, biomedical devices, industrial equipment, battery reinforcement, and explosion protection functions, as well as vibration dampening and shock absorption. To address the associated challenges, we propose future research directions to fully exploit nanoparticle‐enhanced STFs and provide important insights for researchers and practitioners in this dynamic area. [ABSTRACT FROM AUTHOR]

The polyphenylene sulfide (PPS) mesh-based polysulfone (PSF)-zirconia (ZrO 2) composite diaphragm represents a new type of high-performance diaphragm for alkaline water electrolysis hydrogen production, offering low area resistance and high chemical stability. In this study, composite diaphragms with excellent performance are prepared using preheated compression molding, phase inversion precipitation, and vacuum stirring degassing techniques. The comprehensive performance of the prepared diaphragm is compared to that of the commercial Zirfon® diaphragm. The results indicate that the prepared composite diaphragm, with a thickness of 140 μm, exhibits excellent performance. Compared to the Zirfon® UTP 220 diaphragm, the ultra-thin composite diaphragm demonstrates a reduction in area resistance from 0.19 Ω cm2 to 0.1 Ω cm2, an increase in bubble point pressure from 2.31 bar to 2.46 bar, and a voltage of 1.84 V at 1000 mA cm−2. The incorporation of the PPS mesh resulted in a substantial improvement in tensile strength. The application of an ultra-thin composite diaphragm based on PPS mesh can significantly enhance the efficiency of hydrogen production via alkaline water electrolysis. [Display omitted] • Hot-pressing, phase inversion, and vacuum stirring degassing techniques are adopted. • Sponge pore structure improves the bubble point pressure of composite diaphragms. • Ultra-thin composite diaphragm with low area resistance and cell voltage. • It can work continuously and stably in a high-intensity electrolysis environment. [ABSTRACT FROM AUTHOR]

Simple Summary: Poplar forests are significantly threatened by Hyphantria cunea in China. Although previous studies have identified variations in resistance among the different poplar clones to this pest, the induced mechanisms behind the resistance are not yet well understood. This research investigated the dynamic changes in the defensive enzymes and metabolic profiles in resistant '2KEN8' and susceptible 'Nankang' with or without feeding by H. cunea. The findings suggested that the resistant poplar clone initiated an earlier and stronger accumulation of defensive enzymes, and metabolites such as phenolic compounds, flavonoids, and unsaturated fatty acids than the susceptible one after infestation. These changes might contribute to inhibition of larva development in '2KEN8'. The present results are helpful for revealing the mechanisms of poplar resistance to H. cunea and breeding resistant varieties. Poplar trees are significant for both economic and ecological purposes, and the fall webworm (Hyphantria cunea Drury) poses a major threat to their plantation in China. The preliminary resistance assessment in the previous research indicated that there were differences in resistance to the insect among these varieties, with '2KEN8' being more resistant and 'Nankang' being more susceptible. The present study analyzed the dynamic changes in the defensive enzymes and metabolic profiles of '2KEN8' and 'Nankang' at 24 hours post-infestation (hpi), 48 hpi, and 96 hpi. The results demonstrated that at the same time points, compared to susceptible 'Nankang', the leaf consumption by H. cunea in '2KEN8' was smaller, and the larval weight gain was slower, exhibiting clear resistance to the insect. Biochemical analysis revealed that the increased activity of the defensive enzymes in '2KEN8' triggered by the feeding of H. cunea was significantly higher than that of 'Nankang'. Metabolomics analysis indicated that '2KEN8' initiated an earlier and more intense reprogramming of the metabolic profile post-infestation. In the early stages of infestation, the differential metabolites induced in '2KEN8' primarily included phenolic compounds, flavonoids, and unsaturated fatty acids, which are related to the biosynthesis pathways of phenylpropanoids, flavonoids, unsaturated fatty acids, and jasmonates. The present study is helpful for identifying the metabolic biomarkers for inductive resistance to H. cunea and lays a foundation for the further elucidation of the chemical resistance mechanism of poplar trees against this insect. [ABSTRACT FROM AUTHOR]

E. coli is a virulent and opportunistic pathogen with the ability of antibiotic-resistant. In general, E. coli can form the biofilm on food, surfaces, and equipment of the food industry. The high resistance of biofilm to chemical disinfectants has become a big concern for the food industry nowadays due to existence of extracellular polymer. Therefore, many studies were performed for the examination of factors related to biofilm development and destruction specifically for E. coli. The main focus of the present article is an overview of studies related to current chemical, physical, and natural methods as well as nanotechnology in order to control and remove the biofilm of E. coli. It is important to choose a safe, less toxic, and eco-friendly method to combat biofilm of E. coli. Compared with different strategies, it can be said that natural methods (bacteriophages, enzymes, organic acids, and essential oils), physical procedure (electrolyzed water, plasma, and irradiation), and nanotechnology are introduced as appropriate and suitable approaches in different investigations. [ABSTRACT FROM AUTHOR]

Background: Teeth are the anatomical tissue with the highest resistance to the action of chemical and physical agents. This is one of the reasons that make teeth particularly useful in the identification process of skeletonized and carbonized human remains. The aim of this research is to analyze the colorimetric changes in the enamel of teeth subjected to high temperatures to develop a reproducible colorimetric cataloging method. Methods: Six groups of 21 human teeth extracted from private clinics and from a Dental School for therapeutic reasons were used and subjected to three temperature ranges in a laboratory furnace: 400 °C, 700 °C, and 1000 °C. For each temperature, two time periods of 20 min and 60 min were chosen. Each group of dental elements was analyzed using a dental spectrophotometer to extract the colorimetric data of the crown. The obtained color coordinates were subsequently converted into Red–Green–Blue (RGB) values. The two predominant colors were also selected to create average colorimetric values, which demonstrate the change in color hue according to temperature. The groups of teeth subjected to 20 min at 400 °C exhibited a dark gray coloration, while the teeth subjected to 20 min at 700 °C showed a general increase in color brightness with beige–blueish hues. Results: The teeth subjected to 20 min at 1000 °C displayed progressively lighter shades with pinkish reflections. The teeth subjected to 60 min at the same temperatures demonstrated a general increase in brightness, making differentiation more challenging, except for the group of teeth burned at 400 °C, which showed light gray–blueish tones. Conclusions: This study further supports the existing literature on the correlation between colorimetric shifts in carbonized teeth and the maximum temperature reached, providing valuable assistance to forensic pathology and the forensic dental identification of burnt human remains. Additionally, this research has led to the development of a standardized colorimetric patented scale for the observation and examination of burnt human teeth. [ABSTRACT FROM AUTHOR]

Additive manufacturing has profoundly influenced the aerospace industry since its inception, offering unmatched design freedom, cost reduction, rapid prototyping, and enhanced supply-chain efficiency. High-performance polymers like ULTEM™ and PEEK have emerged, known for their strength, temperature resistance, chemical resistance, and lightweight properties. However, the mechanical properties of materials produced through additive manufacturing can vary due to several factors in the printing process, leading to some degree of uncertainty. To address this, the mechanical properties of ULTEM™ 9085 and ULTEM™ 1010 were characterized through mechanical tests. These tests aimed to provide valuable insights into the performance of these materials to be able to run more practical and precise analyses in concurrent design facilities for topological optimization. The results were also compared to materials used in traditional manufacturing methods for components such as flexures and compliant mechanisms. While not fully able to replace metals in high-stress environments, they can be effectively utilized in specific applications. The tests performed contribute to the building of databases that would allow for faster access to critical data that could be applied to a simulation to predict structural performance. This research highlights the potential of additive manufacturing to revolutionize material use in the aerospace sector. [ABSTRACT FROM AUTHOR]

This review explores significant advancements in polymer science and fabrication processes that have enhanced the performance and broadened the application scope of microfluidic devices. Microfluidics, essential in biotechnology, medicine, and chemical engineering, relies on precise fluid manipulation in micrometer-sized channels. Recent innovations in polymer materials, such as flexible, biocompatible, and structurally robust polymers, have been pivotal in developing advanced microfluidic systems. Techniques like replica molding, microcontact printing, solvent-assisted molding, injection molding, and 3D printing are examined, highlighting their advantages and recent developments. Additionally, the review discusses the diverse applications of polymer-based microfluidic devices in biomedical diagnostics, drug delivery, organ-on-chip models, environmental monitoring, and industrial processes. This paper also addresses future challenges, including enhancing chemical resistance, achieving multifunctionality, ensuring biocompatibility, and scaling up production. By overcoming these challenges, the potential for widespread adoption and impactful use of polymer-based microfluidic technologies can be realized. [ABSTRACT FROM AUTHOR]

Microbial toxicity tests play an important role in various scientific and technical fields including the risk assessment of chemical compounds in the environment. There is a large battery of normalized tests available that have been standardized by ISO (International Organization for Standardization) and OECD (Organization for Economic Co-operation and Development) and which are worldwide accepted and applied. The focus of this review is to provide information on microbial toxicity tests, which are used to elucidate effects in other laboratory tests such as biodegradation tests, and for the prediction of effects in natural and technical aqueous compartments in the environment. The various standardized tests as well as not normalized methods are described and their advantages and disadvantages are discussed. In addition, the sensitivity and usefulness of such tests including a short comparison with other ecotoxicological tests is presented. Moreover, the far-reaching influence of microbial toxicity tests on biodegradation tests is also demonstrated. A new concept of the physiological potential of an inoculum (PPI) consisting of microbial toxicity tests whose results are expressed as a chemical resistance potential (CRP) and the biodegradation adaptation potential (BAP) of an inoculum is described that may be helpful to characterize inocula used for biodegradation tests. Key points: • Microbial toxicity tests standardized by ISO and OECD have large differences in sensitivity and applicability. • Standardized microbial toxicity tests in combination with biodegradability tests open a new way to characterize inocula for biodegradation tests. • Standardized microbial toxicity tests together with ecotoxicity tests can form a very effective toolbox for the characterization of toxic effects of chemicals. [ABSTRACT FROM AUTHOR]

Plastic pollution is a problem that threatens the future of humanity, and various methods are being researched to solve it. Plastic biodegradation using microorganisms is one of these methods, and a recent study reported that plastic-degrading microorganisms activated by plasma increase the plastic decomposition rate. In contrast to microbial sterilization using low-temperature plasma, microbial activation requires a stable plasma discharge with a low electrode temperature suitable for biological samples and precise control over a narrow operating range. In this study, various plasma characteristics were evaluated using SDBD (Surface Dielectric Barrier Discharge) to establish the optimal conditions of plasma that can activate plastic-degrading microorganisms. The SDBD electrode was manufactured using low-temperature co-fired ceramic (LTCC) technology to ensure chemical resistance, minimize impurities, improve heat conduction, and consider freedom in designing the electrode metal part. Plasma stability, which is important for microbial activation, was investigated by changing the frequency and pulse width of the voltage applied to the electrode, and the degree of activation of plastic-degrading microorganisms was evaluated under each condition. The results of this study are expected to be used as basic data for research on the activation of useful microorganisms using low-temperature plasma. [ABSTRACT FROM AUTHOR]

Background: Pyrethroid chemicals are one of the main acaricides used against ticks. Resistance to these chemicals has been reported to be associated with mutations in the voltage-gated sodium channel (VGSC) gene of the Rhipicephalus microplus. This study investigates R. microplus resistance to pyrethroids in Guangxi region of China, marking one of the first research efforts in this area. The findings are intended to provide vital baseline for the effective implementation of localized tick control strategies. Methods: From March to July 2021, 447 R. microplus tick samples were collected from five prefecture-level cities in Guangxi. Allele-specific polymerase chain reaction (AS-PCR) was used to amplify segments C190A and G215T of the domain II S4-5 linker and T2134A of domain III S6 in the VGSC, to detect nucleotide mutations associated with resistance to pyrethroid acaricides. Subsequent analyses were conducted to ascertain the prevalence, types of mutations, and genotypic distributions within the sampled populations. Results: Mutations within VGSC gene were identified across all five studied populations of R. microplus, although the mutation rates remained generally low. Specifically, the most prevalent mutation was C190A, observed in 4.9% of the samples (22/447), followed by G215T at 4.0% (18/447), and T2134A at 1.3% (6/447). The distribution of mutations across three critical sites of the VGSC gene revealed four distinct mutation types: C190A, G215T, C190A + G215T, and T2134A. Notably, the single mutation C190A had the highest mutation frequency, accounting for 4.3%, and the C190A + G215T combination had the lowest, at only 0.7%. The analysis further identified seven genotypic combinations, with the wild-type combination C/C + G/G + T/T predominating at a frequency of 90.4%. Subsequently, the C/A + G/G + T/T combination was observed at a frequency of 4.3%, whereas the C/C + T/T + T/T combination exhibited the lowest frequency (0.2%). Additionally, no instances of simultaneous mutations at all three sites were detected. Geographical differences in mutation types were apparent. Both samples from Hechi to Chongzuo cities exhibited the same three mutation types; however, C190A was the most prevalent in Hechi, while G215T dominated in Chongzuo. In contrast, samples from Beihai to Guilin each exhibited only one mutation type: G215T occurred in 12.5% (4/32) of Beihai samples, and C190A in 7.5% (4/53) of Guilin samples. Conclusions: These findings underscore the relatively low frequency of VGSC gene mutations in R. microplus associated with pyrethroid resistance in the Guangxi, China. Moreover, the variation in mutation types and genotypic distributions across different locales highlights the need for regionalized strategies in monitoring and managing pyrethroid resistance in tick populations. This molecular surveillance is crucial for informing targeted control measures and mitigating the risk of widespread resistance emergence. [ABSTRACT FROM AUTHOR]

With the development of the ageing society, wearable strain sensors have great application prospects in the fields of health detection, artificial intelligence, and motion recognition. However, traditional forms of film‐like strain sensors suffer from low sensitivity, adhesion, and impermeability during use, which severely limit their practical applications. To overcome these problems, we propose a strategy to fabricate polyurethane/polydopamine/MXene (TPU/PDA/MXene) composite fibers by wet spinning. Furthermore, the outside is wrapped with (PDMS), giving mechanical strength and chemical resistance. Through a simple and low‐cost wet spinning process, TPU/PDA/MXene fibers are achieved in the preparation of flexible strain sensors, and they can be woven into various forms with good flexibility and comfort according to practical needs. The results indicated that the prepared flexible strain sensor exhibits a high gauge factor (GF) of 57.15 over a large strain range (300 %), which are superior to those of many fiber‐based sensors. Their application properties were also measured by attaching them to fingers, wrists and knees, showing high sensitivity, mechanical durability and chemical stability, and has great potential for wearable strain sensors and flexible strain sensors in complex environments. [ABSTRACT FROM AUTHOR]

We present metalorganic chemical vapor deposition-grown III-nitride tunnel junction (TJ) devices showing negative differential resistance (NDR) under forward bias with a peak to valley ratio of 1.3 at room temperature. Previously, NDR in GaN material systems has only been achievable utilizing molecular beam epitaxy or polarization enhanced AlGaN interlayers. The TJ devices presented here utilize structures based on p+InGaN/n+InGaN materials with the n-side of the junction doped with both Si and Mg and with electron and hole concentrations roughly in the 1019 cm−3 range. The Mg precursor flow is maintained at a constant rate during the whole TJ growth. This co-doped technique can eliminate several Mg-related issues such as delayed incorporation, the memory effect, and Mg solid-state diffusion. Structures grown on relaxed InGaN semibulk templates show enhanced hole concentrations and improved TJ performance. [ABSTRACT FROM AUTHOR]

Vitrimers exhibit unique properties, such as thermal recyclability akin to thermoplastics, while structurally mirroring thermosets in terms of strength, durability, and chemical resistance. However, a significant limitation of these materials is their dependence on an external catalyst. Consequently, this research aims to develop vitrimer materials that incorporate an intrinsic catalyst, thus maintaining excellent thermomechanical properties and recyclability. Polyaddition polymerization is employed to synthesize the desired polymer, incorporating a self‐synthesized tertiary amine unit, (bis(2‐hydroxyethyl)‐3,3′‐((2‐(dimethylamino)ethyl)azanediyl)dipropanoate) (N‐diol), as an internal catalyst for transcarbamoylation and potential transesterification reactions. The resulting polymer, with a gel content of 97% and a glass transition temperature of 29 °C, is fabricated into test samples for comprehensive thermal and mechanical evaluations. The material demonstrates an initial Young's modulus of 555 MPa, retaining 81% of this value after two recycling processes. Additionally, using stress relaxation analysis (SRA), a topology freezing temperature of 82 °C, indicative of the characteristic Arrhenius‐like relaxation behavior, is identified with a bond exchange activation energy of 163 kJ mol−1. [ABSTRACT FROM AUTHOR]

Gd 2 Zr 2 O 7 is considered a promising host material for immobilizing high-level radioactive waste. However, its interplay between grain sizes, radiation resistance and chemical stability is not well understood yet. Herein, Gd 1.7 Nd 0.3 Zr 0.5 Ce 1.5 O 7 ceramics with defect-fluorite phase and three different grain sizes (96, 390 and 1959 nm) were successfully fabricated and irradiated by 140 keV He ion beam up to a fluence of 8 × 1017 ions/cm2. Phase evolutions, microstructure changes and chemical stabilities were investigated. The nano-grained ceramic exhibits the lowest degree of amorphization and a delayed irradiation-induced lattice expansion and damage evolution process, demonstrating an enhanced ability in suppressing the coalescence of He bubbles inside the grain. Grain boundaries parallel to the surface were found to be more favorable sinks for irradiation-induced defects. Chemical stability tests showed that the 42 days leaching rates of all elements were between 10−7∼10−5 g/m2·d. All samples have maintained this superior chemical stability even after irradiation. Interestingly, the leaching test results also suggested that grain size may be not the primary factor influencing the long-term leaching rate. [ABSTRACT FROM AUTHOR]

Gel‐spinning of ultra‐high molecular weight polyethylene (UHMWPE) fibers has attracted great interest in academia and industry since its birth and commercialization in the 1980s, due to unique properties such as high modulus, low density, and excellent chemical resistance. However, the high viscosity and long relaxation time greatly complicate processing. In industry, solvents, like decalin and paraffin oil, usually disentangle the physical networks and promote final drawability. From extruding the polymer solution to post‐solid‐stretching, many polymer physics problems that accompany high‐modulus fiber gel‐spinning should be understood and addressed. In this review, by detailed discussions about the effect of entanglements and intracrystalline chain dynamics on the mechanical properties of UHMWPE, theoretical descriptions of the structure formation of disentangled UHMWPE crystals, and the origin of high modulus and strength of final fibers are provided. Several physical intrinsic key factors are also discussed, revealing why UHMWPE is an ideal material for producing high‐performance fibers. [ABSTRACT FROM AUTHOR]

This study aimed to develop PSU membranes by adding different concentrations (zero, 0.5, 1.0, and 1.5 wt.%) of graphene nanoplatelets (GNP) during synthesis to evaluate the influence of GNP on membrane permeability, retention capacity, mechanical and chemical resistance, structure, and membrane chemistry. All produced membranes had a hydrophilic character, which reduced with the increase in GNP content (72.4° to 84.4°) and a decrease in thickness (200.8 µm to 109.3 µm). Adding GNP did not affect the membranes' mechanical properties and chemical resistance. GNP addition increased the compaction time (from 5.35 h to 35.62 h) and reduced membrane permeability (from 6.78 L∙m−2∙h−1∙bar−1 to 0.10 L∙m−2∙h−1∙bar−1) of pure water. The obtained membranes were classified as ultrafiltration membranes, with an egg albumin retention rate (45 kDa) above 80 %. A greater retention of egg albumin was observed with the highest amount of GNP (1.5 wt.%). Adding GNP stabilized the polymeric matrix (PSU) properties, including increased chemical and mechanical resistance, interaction between the polymer and the nanofiller, and hydrophobic characteristics with a smaller thickness. This study contributed to Brazilian research in membrane synthesis, promoting the investigation of outstanding materials in the field of nanotechnology, in particular, the use of GNP as an additive in the preparation of mixed matrix membranes for water treatment. [ABSTRACT FROM AUTHOR]

Alkali-activated materials (AAMs) are favoured for their low carbon emissions, excellent mechanical properties, and excellent chemical resistance. In this paper, ternary alkali-activated cementitious materials were prepared from slag, steel slag, and lithium slag to investigate their strength and resistance to sulphate attack. A series of experiments were conducted using a variety of material combinations, alkali activator combinations, water–binder ratios, and exposure environments. These experiments employed both macro and micro comparative analyses. The hydration reaction products, physical phase composition, and microstructure of the ground granulated furnace slag, lithium slag, and steel slag (GLS) ternary AAMs were analysed using x-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS). It was experimentally demonstrated that the GLS ternary AAMs had excellent compressive strength, good resistance to sodium sulphate erosion, and that resistance to magnesium sulphate erosion decreased with time. This study contributes to the advancement of knowledge regarding the utilisation of lithium slag and steel slag, and offers new insights into the field of alkali-activated cementitious materials and their resistance to sulphate erosion. [ABSTRACT FROM AUTHOR]

This study aims to develop alkyd-aldehyde and alkyd-ketone blends by modification of waste poly(ethylene terephthalate) (PET) based alkyd resin with urea-aldehyde (UA) and cyclohexanone formaldehyde (CHF) resins for use in coating applications. PET flakes were depolymerized by simultaneous hydrolysis-glycolysis reaction, and depolymerization product (DP) was used completely instead of the diol in the alkyd synthesis. For comparison, reference alkyds without PET were also synthesized. The effect of modifier resin at different ratios and the presence of DP on the coating and thermal properties of blend films were investigated. Medium-hard/hard and gloss/high gloss films with excellent adhesion and impact resistance were obtained from both blends. These films also demonstrated superior chemical and environmental resistance. Blends with CHF resin had better alkali resistance than those with UA resin. In PET-based blends, thermal resistance significantly increased with the addition of the CHF resin to the alkyd resin. Notably, the use of DP did not show a negative effect on the properties of alkyd resin and blend films. On the contrary, much better results were obtained than the alkyd resin alone. Overall, the modification with UA and CHF modifiers and using DP improved the coating properties of the blends. These blends are expected to be considered a sustainable and environmentally friendly alternative for designing versatile coatings for various applications. [ABSTRACT FROM AUTHOR]

A CO 2 -stable, easily sintered proton-conducting oxide electrolytes based on solid solution Ba 7 In 6 Al 2– x Zn x O 19-0.5 x with hexagonal structure has been synthesized for the first time. Within the homogeneity region (0 ≤ x ≤ 0.10), there is an increase in unit cell parameters, cell volumes and free cell volumes. The addition of Zn2+ markedly improved the sinterability of the material. The relative density of the ceramics of the doped samples reached 95 % at lower sintering temperatures than the parent phase. The electrical conductivity was studied using electrochemical impedance spectroscopy. Upon doping the oxygen-ion conductivity increased by 0.25 orders of magnitude at 800 °C. Proton transport was predominant below 500 °C for a wet atmosphere (pH 2 O = 1.92·10−2 atm). The investigated phases Ba 7 In 6 Al 2– x Zn x O 19-0.5 x are capable of hydration and incorporate up to 1.45 mol H 2 O vs 0.41 mol H 2 O for the parent phase. The studied phases exhibit chemical resistance to CO 2 under heat treatment at 600 °C. It was shown that solid solution Ba 7 In 6 Al 2– x Zn x O 19-0.5 x is a promising electrolyte material for intermediate-temperature fuel cells. [Display omitted] • The Zn-doping in solid solution Ba 7 In 6 Al 2– x Zn x O 19-0.5 x markedly improved the sinterability of the material and well-sintered ceramics were obtained with relative density 95 %. • The water uptake increased with increasing Zn-concentration. • Ba 7 In 6 Al 2– x Zn x O 19-0.5 x phases were protonic conductors at T < 500 °C in wet air. • Ba 7 In 6 Al 2– x Zn x O 19-0.5 x phases exhibited chemical resistance to pure CO 2. [ABSTRACT FROM AUTHOR]

Poly(ethylene terephthalate) (PET) is widely used for its high strength‐to‐weight ratio, gas barrier properties, and chemical resistance. The growing PET use highlights the demand for a better recycling system. Enzymatic recycling, alongside mechanical and chemical methods, is eco‐friendly and yields properties similar to virgin PET. Substrate properties (Tg, crystallinity, and specific surface area [SSA]) and enzyme stability significantly impact conversion efficiency. Higher SSA and lower crystallinity tend to yield improved depolymerization when employing leaf compost‐cutinase (LCC‐ICCG) enzymes. This study explored melt extrusion and foaming as pretreatment techniques to modify PET structural properties, using a low‐cost chemical foaming agent (CFA). The monomer conversion rate and efficiency during depolymerization were measured and related to the processing, extrudate micro‐ and meso‐structure, and polyester type. Pretreated PET substrates showed reduced Tg, crystallinity, density, and enhanced SSA, resulting in a 90% mass loss for foamed RPET and VPET substrates within 2 days. In contrast, PET with ~30% of cyclohexanedimethanol comonomer exhibited a nearly 50% lower depolymerization rate, with zero BHET production. It indicates that the combination of low crystallinity, low Tg, and high SSA leads to improved monomer conversion. These findings emphasize the significance of amorphization and foaming in enhancing PET enzymatic depolymerization. [ABSTRACT FROM AUTHOR]

Polyamide (PA) composites exhibit excellent properties such as stiffness, impact resistance, chemical resistance, and thermal stability, making them widely used in automotive interiors, engine parts, and bodywork. To leverage these advantages, high-content composite materials that enhance the wettability and interfacial adhesion between polyamide 66 (PA66) and glass fiber are essential. In this study, we synthesized linear and hyperbranched amide-based flow modifiers to improve the flowability of PA66 composites. H-NMR and FT-IR analyses confirmed the successful preparation of these structures. FT-IR analysis confirmed the successful synthesis of flow modifiers, showing characteristic amide peaks at 1650 cm−1 and the absence of -NH2 peaks at 3300 cm−1. Five flow modifiers were mixed with PA66 in various ratios using a micro-compounder, and viscosity reduction was confirmed by rotational rheometer measurements. Tensile strength and DMA indicated that PA66 composites with flow modifiers showed improved mechanical properties without significant reduction. Notably, PA66 composites with ACDA exhibited a superior viscosity reduction effect while maintaining mechanical strength. The DMA results indicated that the mechanical properties of PA66 composites with flow modifiers showed no significant reduction. The tensile strength of samples with flow modifiers ranged from 208 to 212 MPa, and the elongation at break was between 8.94 and 9.18%. These findings demonstrate that the synthesized flow modifiers improve the viscosity of PA66 composites while maintaining or enhancing mechanical properties. [ABSTRACT FROM AUTHOR]

The durability problems in Portland cement are related to decalcification of C–S–H; alkali-activated composites are proposed as alternative, focusing on acid exposure and resistance. They were prepared from recycled materials, basic oxygen furnace carbonated and desulfurization slags. The standard material is 100% metakaolin geopolymer compared to slag-based alkali-activated materials (AAMs) with and without reinforcement of fibers (basalt, and cellulose), added in 4 wt%. The acidic environments are H2SO4, HCl, and HNO3N = 2.14 (10, 7.5, and 12.5 wt%, respectively). The chemical resistance is improved by the addition of basalt fibers. The decrease in weight loss is 48% in HNO3 and 47% in HCl for AAM-Bas sample, while for AAM-Cell it is 9% in HCl and 34% in HNO3. The compressive strength of the AAM and AAM-Bas samples remains constant after HCl attack, while this acid attacks cellulose samples, which are stable in HNO3 and have a compressive strength of 10 MPa. [ABSTRACT FROM AUTHOR]

To control spontaneous combustion of sulfide ores, the compound inhibitor was prepared by selecting physical resistance raw materials(Na2CO3), chemical resistance raw materials(Melatonin), Cetyltrimethylammonium bromide(CTMAB) and hydroxyethyl cellulose(HEC). With the help of the simultaneous thermal analyzer, different concentrations of inhibitors were prepared and the thermal behavior of the ore samples with 10, 15, and 20 wt% inhibitor at four heating rates of 5, 10, 15, and 20 K/min was determined. The Flynn-Wall-Ozawa method was applied to calculate the activation energy of sulfide ores with different concentrations. The results showed that: Gradually increasing the heating rate will increase the reaction intensity of each ore sample in the first weight loss stage of thermal decomposition, and then reduce the mass of the ore samples involved in the second weight loss stage; The thermal stability of each resisted ore sample is better than that of the original ore sample; The increase in the concentration of inhibitor can inert the reaction process of ore samples in the thermal decomposition stage, weakening the exothermic effect of ore samples; The inhibitor with 15 wt% had a better effect on preventing spontaneous combustion of sulfide ores, and its property value is higher than other concentrations. [ABSTRACT FROM AUTHOR]

The development of polymer‐based luminescent materials with efficient photoactivated ultralong organic phosphorescence (UOP) is of great importance but very challenging. Herein, a new class of organic phosphorescent luminogens is constructed by attaching phenyl rings and/or ethyl benzoates to the nitrogen atoms of a planar aromatic heterocycle pyrrolodiindole (PDI). The compounds show a significant elevation in phosphorescence emission capability after incorporating the ester group(s). However, they cannot produce room‐temperature phosphorescence in the crystalline state. These observations are identified to be associated with the formation of dimers and excimers and the motions of substituents within the molecules. In this context, the PDI derivatives are doped into epoxy polymers with compact and permanent 3D covalent networks. The resulting polymer films show reversible photoactivated UOP under ambient conditions, with quantum yields and lifetimes of up to 24.4% and 2.03 s, respectively, thereby enabling high‐quality and erasable light printing and multi‐level anti‐counterfeiting applications. In addition, they also exhibit excellent water and chemical resistance. This work is conducive to understanding the generation and decay mechanisms of the triplet excitons of organic luminophores with planar aromatic heterocycles in the crystalline state and provides a direction for the development of high‐performance photoactivated UOP materials. [ABSTRACT FROM AUTHOR]

This review paper investigates novel approaches to the fabrication of fiber-reinforced composites (FRCs) via additive manufacturing (AM), with a focus on improving mechanical properties in polymers, metals, and ceramics while reducing weight of the structures. FRCs have been regarded as the optimal material choice across the automobile, aerospace, and construction industries due to their exceptional characteristics, including high strength-to-weight ratio, elevated stiffness, commendable thermal stability, remarkable fatigue and impact resistance, as well as noteworthy chemical and corrosion resistance. AM plays a significant role in FRCs production by offering design flexibility, product customization, waste reduction, near net shape fabrication, cost-effectiveness, and fast prototyping. This paper initially categorizes AM of FRCs into three categories: AM of polymer-matrix, metal-matrix, and ceramic-matrix composites. These categories are further subdivided based on the types of matrix as well as fibers used. Subsequently, it emphasizes the roles of 4D printing and numerical simulation in AMFRCs. The review concludes by addressing potential applications, existing challenges, and scope of AMFRCs in future research and development. [ABSTRACT FROM AUTHOR]

Increasing the surface quality of porcelain tiles, preferred in public, commercial, and living centers, where human density is high, is one of the crucial goals. Surface applications can be applied on the tiles produced as glazed and unglazed tiles in different versions. In lappato glazed tiles, staining-resistance is of great importance besides glossy-surface and wear-resistance. In this study, technical properties such as staining, chemical agent-resistance, color-parameters, thermal-behavior (heat microscopy), roughness, abrasion resistance, and microstructure of glazes (SEM/EDS) depending on the optimizing grinding time were examined with compared to standard lappato-glaze under the industrial conditions. It was observed that with the increase of the glaze grinding, the whiteness value and the increasing smoothness, and higher staining chemicals resistance and the glaze which has lower characteristic temperatures than the standard. As the surface roughness decreased due to grinding, the number and size of pores in the microstructure decreased. The glassy phase exhibited homogeneous distribution due to the dissolution of anorthite crystals. [ABSTRACT FROM AUTHOR]

The possibility of obtaining high-strength vitrified bricks based on loess by adding 20% of waste glass powder was established. At the same time, the amount of moisture in the material should be close to 10%, which corresponds to the dry-pressing technology. [ABSTRACT FROM AUTHOR]

(1) Background: PETG (polyethylene terephthalate glycol) is a transparent, inexpensive, and versatile thermoplastic biomaterial, and it is increasingly being used for a variety of medical applications in dentistry, orthopedics, tissue engineering, and surgery. It is known to have remarkable properties such as tensile strength, high ductility, and resistance to chemical insults and heat, but it can be affected by various environmental conditions. The aim of the present study was to evaluate the topographical characteristics of four thermoplastic dental appliance materials in relation to water sorption in simulated oral environments (artificial saliva samples with different pH values). (2) Methods: The following four types of PETG clear thermoplastic materials were selected for the present study: Leone (L), Crystal (C), Erkodur (E), and Duran (D). In relation to the desiccation and water-uptake stages, their water sorption (Wsp) and solubility (Wsl) were calculated, and the surface topographies were analyzed on two length scales. The surface roughness was determined using a contact profilometer, and nanoroughness measurements were generated by three-dimensional profiles using an atomic force microscope (AFM). Statistical analyses (one-way ANOVA and unpaired and paired Student t-tests) were performed. (3) Results: After saliva immersion, the weights of all samples increased, and the highest sorption was recorded in a basic environment. Among the materials, the water uptake for the L samples was the highest, and for E, it was the lowest. In relation to water solubility, significant values were registered for both the L and C samples' materials. After immersion and desiccation, a decreasing trend in microroughness was observed. The AFM high-resolution images reflected more irregular surfaces related to saliva immersion. (4) Conclusions: The sorption rates recorded in water-based artificial saliva were higher for basic pH levels, with significant differences between the samples. There were also significant differences related to the behaviors of the materials included in the study. In relation to roughness, on a microscale, the surfaces tended to be smoother after the saliva immersions, and on a nanoscale, they became more irregular. [ABSTRACT FROM AUTHOR]

High-performance ceramics are recognized as key enabling materials because of their very high thermal, chemical and mechanical resistance in combination with a lower density compared to most metals. These properties apparently predestine ceramics for many different applications, e.g. propulsion engines. Within the present work, the high potential of additive manufacturing in the field of ceramic materials (CerAMfacturing) could be demonstrated. It is possible to produce high-resolution ceramic aerospike engines using CerAM VPP. The manufactured components not only combine the typical ceramic properties, but also exhibit: - high geometric complexity, - very good surface properties, and - very good manufacturing accuracy. These developments will pave the way for a new generation of propulsion engines. • Ceramic aerospike engine additively manufactured by CerAM VPP. • No critical defects or deformations visible with NDT. • Very high resolution (slit width approx. 500 μm) and very good surface quality (R a < 2 μm). • Measurements on specific impulse showed very good reproducibility. [ABSTRACT FROM AUTHOR]

Wood adhesives were made using defatted soy flour, casein, sodium hydroxide (NaOH) and ethylene diamine. These eco-friendly wood adhesives are used to substitute formaldehyde-derived adhesives in order to decrease formaldehyde and volatile organic compounds emissions from the adhesives that are utilised in plywood. The features of adhesively-glued wood joints in terms of performance such as tensile strength, water resistance and chemical resistance were gauged in this study. The results revealed that adhesives showing good performance and eco-friendly adhesive system was prepared for wood joints. [ABSTRACT FROM AUTHOR]

Acid resistance testing of concrete – development of a rapid testing method In many applications in agriculture, industry and waste water systems, concrete damage caused by acid attack is the decisive damage mechanism for durability. First, the cement paste on the concrete surface is decomposed by dissolving attack before a diffusion‐inhibiting covering layer forms between the surface and the attack zone. Hereafter, the damaging process progresses diffusion controlled and the damage zone advances into the concrete interior. Finally, progressive surface concrete erosion occurs which becomes decisive for the development of damage. In order to predict durability, it is essential to reliably record all three types of damage‐stages, including their interactions, as part of performance tests. However, this means that long test times of several months are inevitable, thus no meaningful chemical acid resistance tests for quality control are available. However, if the erosion behaviour for a specific concrete composition is known through performance tests, the test duration can be significantly reduced, e.g. for production control. This article presents such a suitable rapid test method for characterizing the acid resistance of concrete, which detects the early damage stages of acid attack quickly and cost‐effectively. The comparability and reproducibility of the test results are demonstrated and the application limits and possibilities are discussed. [ABSTRACT FROM AUTHOR]

This article presents the results of research on the development of chemically resistant polymer–mineral casting composites based on industrial waste. The aim of this work is to develop a technological basis for obtaining effective inorganic fillers and highly filled composites for use in chlorine-containing environments. On the basis of theoretical data, mineral fillers and a polymer binder for filling composites were selected, optimal quantities of input hardeners and an appropriate thermal curing mode were determined, and the influence of the filling degree on the properties of composites was studied. The influence of various factors on the properties of the obtained composites was also studied, and the possibility of using local raw materials to obtain special-purpose composites was investigated. Ash from a thermal power plant (TPP) was used as an acid-resistant filler in composites. Two components were chosen as binders: phenol formaldehyde resin and mineral filler (TPP ash). As the third component, hydrolytically active fillers—anhydrite, phosphogypsum and phosphate slag—were used. The degree of filling has a significant influence on the properties of composites, including the compressive strength, chemical resistance and degree of curing, the values of which were elucidated across a wide range of composite variations based on the degree of filling. The conducted research allowed us to establish the limit of admissible anhydrite content, which should not exceed 15 mas.%. To optimize the chemical resistance and durability of the composites of the investigated substances, the method of mathematical planning was used. According to the results of this study, the optimal compositions of composites, in terms of anhydrite, phosphogypsum and phosphorus slag contents, were selected. At the maximum possible degree of filling, these composites exhibit high target characteristics. [ABSTRACT FROM AUTHOR]

By screening the compounding combination of Wuyiencin and chemical agents, this study aims to delay the emergence of chemical agent resistance, and provide a technical reference for scientific and rational fungicides technology. This study investigated the impacts of the antibiotic wuyiencin derived from Streptomyces albulus var. wuyiensis and its combination with pyrimethanil on the inhibition of Botrytis cinerea. Treatment with wuyiencin (≥80 µg mL−1) strongly inhibited the pathogenicity of B. cinerea and activated the plant defense response against B. cinerea. Application of 80–100 µg mL−1 wuyiencin effectively controlled grape gray mold (by 57.6–88.1% on leaves and 46.7–96.6% on fruits). Consequently, the application of 80–100 µg mL−1 wuyiencin effectively mitigated grape gray mold incidence, leading to a substantial reduction in disease symptoms to nearly imperceptible levels. When wuyiencin (at the median effective concentration [EC50]) was combined with pyrimethanil (EC50) at a ratio of 7:3, it exhibited the highest efficacy in inhibiting B. cinerea growth. This combination was significantly more potent (p < 0.05) than using wuyiencin or pyrimethanil alone in controlling gray mold on grape leaves and fruits. Furthermore, the combination effectively delayed resistance development in gray mold. The experimental results show that wuyiencin can delay resistance development by affecting the expression of methionine biosynthesis genes and reducing the activity of the cell wall-degrading enzyme activity. [ABSTRACT FROM AUTHOR]