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This study reveals one-step green synthesis of plant inspired silver nanoparticles (Ag-NPs). The synthesis procedure relies on the bio-reduction of Ag+ to Ag0 using orange waste (orange peel) extract as cheap, readily available, sustainable, biocompatible feedstocks as a reducing and stabilizing agent. The prepared Ag-NPs passed through a full characterization procedure for better confirmation and elucidation of optical and structural properties. The fluorescence of the prepared Ag-NPs has a quantum yield of 17.15% enabling its potential use in chemical sensing of drugs. Ag-NPs are conceived to be used as a fluorescent nano sensor for sensitive, ecofriendly, rapid spectrofluorimetric determination of two recent direct oral anticoagulants, namely, rivaroxaban (RIV) and edoxaban tosylate monohydrate (EDT); COVID-19 adjunctive drugs in their raw materials and pharmaceutical tablets. The fluorescence of the prepared Ag-NPs at 333 nm (λ ex = 258 nm) was found to be substantially quenched in existence of increasing concentrations of each drug. The quenching mechanisms were studied and explained. The validation of the method revealed linear correlation over the ranges of 0.5–10 µg/ml with an excellent regression correlation (r = 0.9999) for both drugs with minimum detection limits of 0.14 and 0.16 µg/ml for rivaroxaban and edoxaban tosylate monohydrate, correspondingly. Three different metrics were employed for verifying the greenness profile of the presented study. The findings of the greenness assessment were congruent and compatible with the green synthesis procedure, ecofriendly analysis, and the exclusion of using organic solvents and noxious materials opening an avenue for green synthesis of nanoparticles instead of chemical and physical methods. [ABSTRACT FROM AUTHOR]

This study presents the synthesis and characterization of upconverter nanostructures consisting of a perovskite host matrix, CaZrO 3 , co-doped with trivalent ytterbium (Yb3+) and europium (Eu3+), denoted as CaZrO 3 :Yb3+/Eu3+. Single-doped CaZrO 3 :Eu3+ samples were excited using a 394 nm UV source, while CaZrO 3 :Yb3+/Eu3+ samples were excited with a 980 nm diode laser source. Yb3+ ions efficiently absorb the 980 nm light and transfer the absorbed energy to the nearby ion Eu3+ ions, leading to the emission of visible light around 590, 614, and 655 nm, respectively. The emission spectra of Eu3+ ions exhibit an initial increase with increasing Yb3+ concentration, peaking at 7 mol%, followed by a decrease due to luminescence quenching. The decay lifetime of Eu3+ ions under 300 nm excitation decreases simultaneously with increasing Yb3+ concentration, indicating energy migration between Yb3+ and Eu3+. Detailed explanations of the energy transfer mechanism between Yb3+ and Eu3+ ions are provided, supported by equations and diagrams. This study provides valuable insights into the optimization of dopant concentrations for enhancing upconversion luminescence in CaZrO 3 :Yb3+/Eu3+ nanostructures, with 3 mol% Eu3+ concentration identified as optimal based on preliminary experiments. The findings presented in this paper contribute to the understanding of energy transfer processes in luminescence upconversion materials and highlight the potential of CaZrO 3 :Yb3+/Eu3+ nanostructures for applications in lighting, displays, and bio-imaging. This work represents a significant advancement in the field of upconversion luminescence emission, particularly in the utilization of CaZrO 3 codoped with Yb3+ and Eu3+, and lays the foundation for further research in this area. [ABSTRACT FROM AUTHOR]

ABSTRACT Two new luminescent metal–organic frameworks (MOFs), namely, [Zn2(HL)2]n (1) and {[Cd2(HL)2(H2O)2]⋅(H2O)0.5}n (2) [H3L = 5‐((4‐(1H‐1,2,4‐triazol‐1‐yl)benzyl)amino)isophthalic acid ligand], have been solvothermally synthesized and characterized. Single‐crystal x‐ray diffraction shows that 1 exhibits a 3D framework, whereas 2 features 2D network. Furthermore, the fluorescence studies demonstrated that 1 and 2 exhibited luminescent sensing activity for nitrobenzene (NB), Fe3+ ions, and Cr2O72− anions with high selectivity, high sensitivity, and low detection limit, the corresponding detection limits of 1 were 6.40 × 10−7, 1.26 × 10−7, and 1.44 × 10−7 M, respectively, and that of 2 were 2.42 × 10−6, 3.41 × 10−7, and 2.90 × 10−7 M, respectively. 1 and 2 exhibited excellent solvent, pH, and thermal stabilities. The results suggested that both 1 and 2 can be considered as potential fluorescent sensors of NB, Fe3+ ions, and Cr2O72− anions. [ABSTRACT FROM AUTHOR]

Although many dyes have been introduced into cellulose, whether bound to its backbone or within a cellulose matrix, few studies have determined whether the backbone statically or dynamically quenches the photoluminescence of the dye. To advance cellulosic fluorescent films, the influence of the cellulose backbone on photoluminescence must be understood. We determined the fluorescence properties of fluorescein isothiocyanate (FITC) and fluorescein-labeled cellulose (FLC) in water and alcohol, including their quantum yields , lifetimes , and rates of radiative and nonradiative decay. Dissolved FLC had a ~ 30× lower than FITC, suggesting that incorporating FITC into the cellulose backbone remarkably reduces the fluorescence efficiency. The FLC solutions had a six-fold lower than their FITC counterparts but a 10–20 times higher . Presumably, this was because the cellulose backbone interacted weakly with the fluorescein moieties, suggesting a quenching mechanism that can be termed quasi-static, corresponding to static quenching between the fluorescein moieties and cellulose backbone, in addition to the fluorescence quenching caused by the intramolecular nonradiative processes of fluorescein, as observed in conventional molecules. Using the Strickler‒Berg formula, we deduced the analytical radiative decay rate constants and eventually estimated the number of very short-lived fluorescein moieties per single fluorescent fluorescein moiety, corresponding well with static quenching. [ABSTRACT FROM AUTHOR]

Plant-derived carbon dots (P-CDs) are gaining attention in environmental remediation due to their cost-effectiveness, availability, and lower toxicity compared with chemically synthesized carbon dots. This review comprehensively examines the recent advancements in the synthesis and application of P-CDs, with a particular emphasis on their efficacy in the sensing of heavy metals, which are among the most pervasive environmental contaminants. A detailed comparative analysis is presented by evaluating the performance of P-CDs against their chemically synthesized counterparts based on key parameters, such as optimal operating conditions and detection limits. Furthermore, sensing the potential of P-CDs towards every heavy metal ion has been discussed with in-depth mechanistic insights. Additionally, this review explores the industrial applications and future directions of P-CDs. This review provides a comprehensive analysis of -P-CDs for heavy metal sensing, aiming to enhance their sensitivity and selectivity toward heavy metal ions. [ABSTRACT FROM AUTHOR]

Interactions between gold metallic nanoparticles and molecular dyes have been well described by the nanometal surface energy transfer (NSET) mechanism. However, the expansion and testing of this model for nanoparticles of different metal composition is needed to develop a greater variety of nanosensors for medical and commercial applications. In this study, the NSET formula was slightly modified in the size-dependent dampening constant and skin depth terms to allow for modeling of different metals as well as testing the quenching effects created by variously sized gold, silver, copper, and platinum nanoparticles. Overall, the metal nanoparticles followed more closely the NSET prediction than for Förster resonance energy transfer, though scattering effects began to occur at 20 nm in the nanoparticle diameter. To further improve the NSET theoretical equation, an attempt was made to set a best-fit line of the NSET theoretical equation curve onto the Au and Ag data points. An exhaustive grid search optimizer was applied in the ranges for two variables, 0.1 ≤ C ≤ 2.0 and 0 ≤ α ≤ 4 , representing the metal dampening constant and the orientation of donor to the metal surface, respectively. Three different grid searches, starting from coarse (entire range) to finer (narrower range), resulted in more than one million total calculations with values C = 2.0 and α = 0.0736 . The results improved the calculation, but further analysis needed to be conducted in order to find any additional missing physics. With that motivation, two artificial intelligence/machine learning (AI/ML) algorithms, multilayer perception and least absolute shrinkage and selection operator regression, gave a correlation coefficient, R 2 , greater than 0.97 , indicating that the small dataset was not overfitting and was method-independent. This analysis indicates that an investigation is warranted to focus on deeper physics informed machine learning for the NSET equations. [ABSTRACT FROM AUTHOR]

The development of high-performance oxygen evolution reaction (OER) electrocatalysts based on earth-abundant elements is of great significance for the production of hydrogen fuel through water electrolysis. Herein, defect rich NiO nanosheet arrays were synthesized on nickel foam (NF) by rapidly quenching NiO in Al salt solution at 0 °C and followed by partially etching Al in alkaline solution. With the approach, the quenching can simultaneously achieve the required surface metal doping and generation of abundant oxygen vacancies. Moreover, more active sites can be provided for OER due to the leaching of Al during the etching process. As a result, the quenching-etching surface engineering endows the NiO catalyst with the desired advantages, including high conductivity and large specific surface area. The as-obtained optimal electrode (72h Al–NiO/NF) with an etching time of 72 h exhibited much enhanced electrocatalytic activity towards OER in alkaline solution, which needs a low overpotential of 277 mV to achieve 10 mA cm−2 water oxidation current. Furthermore, the catalyst also showed a very low Tafel slope of 51.8 mV dec−1 and excellent durability. The synthesis of defect rich NiO nanosheets through the quenching-etching route confirms the importance of elaborate engineering of material surface for high-performance OER. • Defect rich NiO nanosheet arrays grown on NF were successfully fabricated by a quenching-etching surface engineering route. • The obtained electrode successfully combined the desired merits, including high conductivity and large specific surface area. • The as-obtained 72h Al–NiO/NF shows superior activity, favorable reaction kinetics and robust durability for OER in alkaline media. [ABSTRACT FROM AUTHOR]

In this work, we explore the interaction as well as corona formation and interfacial phenomena of lysozyme (LYZ) and 2D SnSe nanoflake. The optical results indicate formation of ground state complex with an apparent association constant of 1.5 × 103 (mol)−1. The dynamics of the in situ interaction exhibited surface reorganization (t2 = 73.5 min) and unfolding, which were more prominent than binding (t1 = 3 min) for tryptophan residues of LYZ. The formations of soft and hard corona of the LYZ structure were clearly observed from HRTEM. The emission quenching exhibited tertiary deformation of the LYZ structure with positive cooperative binding (n > 1) and dynamics of quenching followed the sigmoidal Boltzmann nature of the energy transfer process. The ultrafast lifetime of the bioconjugate varied from 1.9–1.35 ns with a maximum 63% energy transfer efficiency within 300 min of the corona evolution. The decrement of α helix (58.87%–21.78%) and increment of β sheet (5.27%–23.98%) were observed after interaction, with the conversion of large amount of α helix into β sheet. The ITC results showed that the injection heat results followed two‐site binding model, and the exothermic binding was dominate over the interaction. The second phase binding is driven by larger positive entropy, where the first binding site has a stronger association. [ABSTRACT FROM AUTHOR]

In this study, a quenching experiment was conducted at atmospheric pressure to investigate the flow and heat-transfer characteristics of cylindrical rods made from SS, FeCrAl, and Zr-4 under various subcooling degrees (ΔTsub). The inverse heat-conduction problem (IHCP) method and image-processing technique were utilized to determine the surface temperature and heat flux, vapor film thickness, and quench front propagation. The results show that smaller solid kρcp and larger ΔTsub result in relatively more efficient quenching boiling heat transfer, thinner vapor film thickness, and greater quench front propagation velocity. The quench front originates at the bottom of the test specimen and becomes progressively larger in velocity with time. It eventually converges with the downward-propagating quench front in the upper middle of the test specimen. Moreover, at the beginning of quench front propagation, the SS and FeCrAl test specimens have a constant velocity region. However, because the Zr-4 test specimen has a small kρcp, the velocities gradually increase from the onset of quench front generation. Furthermore, the measured average quench front velocities are consistent with the experimental datum from the literature. However, the predicted model proposed by Duffey underestimates the propagation velocity due to ignoring the cooling effect of film boiling. [ABSTRACT FROM AUTHOR]

Controlling the cooling rate experienced by a material during a manufacturing process is a challenge and a major issue. Industrial processing techniques are very diverse and may involve a whole range of cooling rates, which are sometimes extremely high for small and/or thin manufactured parts. For polymers, the cooling rate has consequences on both the microstructure and the time-dependent properties. The common cooling rates associated with conventional calorimetric measurements are generally limited to a few tens of degrees per minute. This work combines several calorimetric techniques (DSC, modulated-temperature DSC, stochastically-modulated DSC and Fast Scanning Calorimetry) to estimate the critical cooling rate required to melt-quench fast-crystallizing polyesters to their fully amorphous state, based on the example of a series of poly(alkylene trans-1,4-cyclohexanedicarboxylate) (PCHs) with a number of methylene groups in the main structure of the repeating unit n C H 2 varying from 3 to 6. The even-numbered ones require faster cooling rates (about 3000 K s−1 for n C H 2 = 4, between 500 and 1000 K s−1 for n C H 2 = 6) compared to the odd-numbered ones (between 50 K min−1 and 100 K s−1 for n C H 2 = 3, between 10 and 30 K min−1 for n C H 2 = 5). [ABSTRACT FROM AUTHOR]

ABSTRACT Detecting antibiotic residues is crucial for monitoring their excessive use in healthcare and agricultural practices. Herein, a new 3D metal–organic framework (MOF) containing {[Cd (bpyp)(sdba)]·DMF·2H2O}n (1) (bpyp = 2,5‐bis (pyrid‐4‐yl)pyridine and H2sdba = 4,4′‐sulfonyldibenzoic acid) has been designed and synthesized. MOF 1 displays sensitive detection tetracycline (TCY) with a limit of detection below 7.67 × 10−6 M in an aqueous solution. The detection mechanism involves competitive absorption between MOF 1 and antibiotics, supported by UV–vis spectroscopy and fluorescence lifetime measurements. MOF 1 exhibits a visible fluorescence response to TCY under a 254 nm UV lamp. MOF 1 is applied in the quantitative detection of TCY in lake water with the recovery based on the sensing platform was 92.26–107.54% with RSD (%) less than 4.38%, indicating outstanding reliability. [ABSTRACT FROM AUTHOR]

The mechanistic details of a reported allylation reaction are investigated by means of Stern–Volmer experiments and nanosecond transient absorption spectroscopy. Both reference substrates, i.e., an allylic chloride and a trifluoroacetamide, are inefficient quenchers but large quenching rate constants are observed upon the addition of Ni(COD)2 and a bisoxazoline ligand. The large quenching rate constants and absence of observable photoproducts are consistent with a mechanism that operates by energy transfer between the excited-state iridium photosensitizer and the nickel complex. [ABSTRACT FROM AUTHOR]

A profound understanding of the binding dynamics of drugs with plasma proteins is highly important as it determines its therapeutical potential. Herein, we have investigated the molecular interaction of Tucatinib (TUC), a novel, primitive and highly selective drug for treatment of HER2+ advanced unresectable breast cancer, with bovine serum albumin (BSA) using multi‐pronged spectroscopic techniques and molecular docking. TUC considerably quenched the intrinsic fluorescence of BSA via static quenching mechanism, and it binds to the hydrophobic cleft of subdomain IIA of BSA with a moderate binding affinity. The thermodynamic analysis revealed the major interplay of van der Waals forces and hydrogen bonding interactions in stabilising the binding. The Förster distance 'r' signifies feasible energy transfer between BSA and TUC. The conformational analyses indicate some alterations in the protein secondary structure as a consequence of some changes in the protein polar environment due to complex formation. The experimental results are supported by docking analyses. [ABSTRACT FROM AUTHOR]

This study employs the finite element method to investigate the microstructural evolution and deformation behavior of a 40Cr steel automobile front axle during the quenching process. By establishing a multi-physics field coupling model, the study elucidates the variation patterns of the microstructure field in the quenching process of the front axle under different immersion orientations. It is found that along the length direction, the bainite and martensite structures decrease from the center to the edge region, while the ferrite structure shows an increasing trend. Additionally, the influence of immersion orientation on the hardness of the front axle's microstructure and deformation behavior is thoroughly discussed. The results indicate that, firstly, when quenched horizontally, the hardness difference among different regions of the front axle is approximately 8.2 HRC, whereas it reaches 10.3 HRC when quenched vertically. Considering the uniformity of the microstructure, the horizontal immersion method is preferable. Secondly, due to the different immersion sequences in different regions of the front axle leading to varying heat transfer rates, as well as the different amounts of martensite structures obtained in different regions, the deformation decreases along the length direction from the center to the edge region. Horizontal immersion quenching, compared to vertical immersion, results in a reduction of approximately 56.2% and 48.9% in deformation on the representative central cross-section (A-A) and the total length of the front axle, respectively. Therefore, considering aspects such as microstructure uniformity and deformation, the horizontal immersion quenching orientation is more favorable. [ABSTRACT FROM AUTHOR]

The BiFeO3-BaTiO3 (BF-BT) ceramics were here prepared through the solid-state reaction of Bi2O3, Fe2O3 and nano-sized BT powders. The crystal structures and piezoelectric properties were investigated in both quenched (AQ) and slowly cooled (SC) 0.7BF-0.3BT ceramics. Prior work has shown that rhombohedral and pseudo-cubic phases coexist in 0.7BF-0.3BT ceramics. In this work, the crystal structure of the pseudo-cubic phase was refined as a non-polar orthorhombic Pbnm phase in the SC sample and as a polar orthorhombic Pmc21 phase in the AQ sample. In addition to a sharp dielectric peak at about 620 °C, corresponding to the Curie temperature of the rhombohedral phase, a broad dielectric peak with strong frequency dispersion and a sharp frequency-independent dielectric peak were observed at around 500 °C in the SC and AQ samples, respectively. We determine that the dielectric anomalies around 500 °C were caused by a relaxor phase transition of the non-polar orthorhombic phase in the SC sample and a ferroelectric–paraelectric phase transition of the polar orthorhombic phase in the AQ sample. The AQ sample showed better ferroelectric and piezoelectric properties than the SC sample. The 0.7BF-0.3BT ceramic slowly cooled in a nitrogen atmosphere showed a well-saturated P-E curve and a similar temperature-dependent dielectric constant as the AQ sample. Our results indicate that large concentrations of oxygen vacancies produce a more distorted polar orthorhombic phase and better piezoelectric properties in the AQ sample than in the SC sample. [ABSTRACT FROM AUTHOR]

Tungsten carbides are important materials used in ceramic cements, machining tools, catalysts, sensors, and for hydrogen generation. Bulk W–C structures are highly complex; fundamental fully carburized WC and semi-carburized W 2 C are accompanied by structural transitions depending on the composition and temperature. The relationship between the structures, compositions, and temperatures is summarized in the W–C phase diagram. However, the high-temperature, stable, and single-crystalline nanoparticles related to the WC 1-x and W 2 C phases formed via energetic reactions accompanied by rapid cooling rates are not easy to determine considering the bulk phase diagram, and lead to fundamental questions regarding the origin of the nanophases. In this study, we propose a draft for the W–C nanophase diagram composed of the surface and gas-phase WC, WC 1-x , and W 2 C nanophases according to the composition and temperature. The model undergoes the process of a vapor–nanoliquid–nanophase starting from the gas-phase nucleation induced by an extremely high-temperature electrical explosion. In addition, the high-temperature reactivity and quenched nanophase, including its unique nanostructure, are related to the post-melt rheology, physical morphology, and steric hindrance of the solid matrix during an electrical explosion. [ABSTRACT FROM AUTHOR]

It is a fluorescence-based study to examine the interaction between L-tryptophan and a selection of aldehydes, namely furfural (furan-2-carbaldehyde), 3-hydroxybenzaldehyde, salicylaldehyde (2-hydroxybenzaldehyde), 3-nitrobenzaldehyde, and 4-bromobenzaldehyde. The investigation took place in an aqueous environment, revealing that all five aldehydes induced quenching of the fluorescence intensity of L-tryptophan. By employing the Stern-Volmer equation to describe the quenching process, we constructed Stern-Volmer plots and derived Stern-Volmer constants. These constants (KSV) ranged from 2.87 × 104 mol L− 1 to 5.75 × 104 mol L− 1. Notably, the values of the Stern-Volmer constants varied among the different aldehydes, with the following order: 3-hydroxybenzaldehyde(3-HBA) > 4-bromobenzaldehyde (4-BBA) > 3-nitrobenzaldehyde > furan-2-carbaldehyde > salicylaldehyde. Consequently, our findings highlighted 3-hydroxybenzaldehyde as the most potent quencher, while 2-hydroxybenzaldehyde displayed the least sensitivity to quenching. Additionally, we determined the detection and quantification limits for the investigated aldehydes, resulting in ranges of 3.87 × 10− 12 to 8.25 × 10− 6 and 1.29 × 10− 11 to 2.75 × 10− 5, respectively. This research paves the way for the development of novel fluorescence probe-based sensors and offers valuable techniques for analyzing aldehydes within environmental and biological samples. [ABSTRACT FROM AUTHOR]

A detailed spectroscopic study (fluorescence, absorption, and lifetime) was conducted to gain insight into the nature of the binding interaction between fluorophore Hoechst33258 (H258) and jaundice marker Bilirubin (Br). The fluorescence emission of the H258 (Ex/Em = 340-502nm) showed a conc. dependent quenching in the presence of Br (1.25 μ M to 10 μ M). The Stern-Volmer constant demonstrated an upward curve depicting the occurrence of both static and dynamic quenching with an acquired value of K SV = 3.1x 10 3 M - 1 and biomolecular quenching rate constant K q = 8.6 x 10 11 M - 1 S - 1 . The static quenching was evaluated using the sphere of action model and a sphere radius of 0.3nm indicated the presence of a static component in the quenching. The FRET analysis with overlap integral (J) = 1.4x10 14 M - 1 cm - 1 nm 4 and Foster Radius(R 0 ) = 26.82 Å with 59% efficiency suggested occurrence of dynamic quenching. Further studies with the time-resolved fluorescence also indicated the presence of dynamic quenching. The lifetime values of H258 reduced from 3.9ns to 0.5ns. Molecular docking studies further support both static and dynamic components in quenching. A non-covalent interaction of H258 with Br in the presence of HSA is predominantly characterized by H-bonding with residues Lys, Asn, Glu, Gln, and Br. The H258 and Br interaction was within the distance of 3.04 Å, which is in coherence with the sphere of action model (0.3nm) and Van-der-Waals along with hydrophobic interactions, which suggested both static and dynamic quenching. Thus, H258 can serve as an efficient fluorophore to monitor binding interactions and can be further exploited as a suitable probe for investigating conformational changes and detection of Br in subsequent studies. [ABSTRACT FROM AUTHOR]

This paper explores the effects and impacts of the metallurgical process of quenching on grain-oriented strips of electrical steel. Experimental findings reveal that quenching resulted in increased hardness and an increased Young's modulus. An analysis of the material structure post-quenching indicates significant alterations in grain spacing and reduced height differences between grains. However, the magnetic properties of the steel deteriorated following quenching. [ABSTRACT FROM AUTHOR]

Formation of stacking fault tetrahedra and diffuse streaks along (111) in the equiatomic Cr-Co-Ni medium-entropy alloy subjected to different heat-treatments and different specimen preparation methods are examined by transmission electron microscopy. Neither stacking faults nor stacking fault tetrahedra are formed simply by quenching from a high temperature due to the high energy barrier for the formation and migration of vacancies. These defects, however, are found to form by Ar+-ion irradiation, as abundant vacancies are continuously introduced during ion-irradiation so as to bypass the high energy barrier for the formation. Diffuse streaks along (111) are usually observed in the SAED pattern with the (111) incidence regardless of heat-treatments and specimen preparation methods, indicating the occurrence of diffuse streaks is nothing to do with the formation of stacking faults and stacking fault tetrahedra. [ABSTRACT FROM AUTHOR]

Abstract This study reveals one-step green synthesis of plant inspired silver nanoparticles (Ag-NPs). The synthesis procedure relies on the bio-reduction of Ag+ to Ag0 using orange waste (orange peel) extract as cheap, readily available, sustainable, biocompatible feedstocks as a reducing and stabilizing agent. The prepared Ag-NPs passed through a full characterization procedure for better confirmation and elucidation of optical and structural properties. The fluorescence of the prepared Ag-NPs has a quantum yield of 17.15% enabling its potential use in chemical sensing of drugs. Ag-NPs are conceived to be used as a fluorescent nano sensor for sensitive, ecofriendly, rapid spectrofluorimetric determination of two recent direct oral anticoagulants, namely, rivaroxaban (RIV) and edoxaban tosylate monohydrate (EDT); COVID-19 adjunctive drugs in their raw materials and pharmaceutical tablets. The fluorescence of the prepared Ag-NPs at 333 nm $${(\uplambda }_{\text{ex}}=258 \text{nm})$$ ( λ ex = 258 nm ) was found to be substantially quenched in existence of increasing concentrations of each drug. The quenching mechanisms were studied and explained. The validation of the method revealed linear correlation over the ranges of 0.5–10 µg/ml with an excellent regression correlation (r = 0.9999) for both drugs with minimum detection limits of 0.14 and 0.16 µg/ml for rivaroxaban and edoxaban tosylate monohydrate, correspondingly. Three different metrics were employed for verifying the greenness profile of the presented study. The findings of the greenness assessment were congruent and compatible with the green synthesis procedure, ecofriendly analysis, and the exclusion of using organic solvents and noxious materials opening an avenue for green synthesis of nanoparticles instead of chemical and physical methods.

Abstract Although many dyes have been introduced into cellulose, whether bound to its backbone or within a cellulose matrix, few studies have determined whether the backbone statically or dynamically quenches the photoluminescence of the dye. To advance cellulosic fluorescent films, the influence of the cellulose backbone on photoluminescence must be understood. We determined the fluorescence properties of fluorescein isothiocyanate (FITC) and fluorescein-labeled cellulose (FLC) in water and alcohol, including their quantum yields $$\boldsymbol{\phi}_{\textit{\textbf{PL}}}$$ , lifetimes $${\boldsymbol{\tau}}$$ , and rates of radiative $${\textit{\textbf{k}}}_{\textit{\textbf{r}}}$$ and nonradiative $${\textit{\textbf{k}}}_{\textit{\textbf{nr}}}$$ decay. Dissolved FLC had a ~ 30× lower $$\boldsymbol{\phi}_{\textit{\textbf{PL}}}$$ than FITC, suggesting that incorporating FITC into the cellulose backbone remarkably reduces the fluorescence efficiency. The FLC solutions had a six-fold lower $${\textit{\textbf{k}}}_{\textit{\textbf{r}}}$$ than their FITC counterparts but a 10–20 times higher $${\textit{\textbf{k}}}_{\textit{\textbf{nr}}}$$ . Presumably, this was because the cellulose backbone interacted weakly with the fluorescein moieties, suggesting a quenching mechanism that can be termed quasi-static, corresponding to static quenching between the fluorescein moieties and cellulose backbone, in addition to the fluorescence quenching caused by the intramolecular nonradiative processes of fluorescein, as observed in conventional molecules. Using the Strickler‒Berg formula, we deduced the analytical radiative decay rate constants $${\textit{\textbf{k}}}_{\textit{\textbf{r}}}^{\textit{\textbf{S.B.}}}$$ and eventually estimated the number of very short-lived fluorescein moieties per single fluorescent fluorescein moiety, corresponding well with static quenching.

The effects of quenching and tempering temperatures on the microstructure and mechanical properties of super martensitic stainless steel (SMSS) 00Cr13Ni5Mo were studied. The SMSS after heat treatment is composed of martensite (α phase) and a small amount of austenite. When the quenching temperature is 930 °C, with the increase of tempering temperature, the enrichment of Ni in martensite leads to the formation of reverse austenite, the content of martensite phase decreases from 84.9 % to 80.0 %, and the average grain size increases from 23.23 μm to 27.07 μm. When tempering at 580 °C, the content of martensite phase decreases from 80.0 % to 83.7 % with the increase of quenching temperature. The average grain size increased from 25.23 μm to 35.01 μm. When the quenching temperature is 930 °C, the hardness and yield strength of SMSS decrease, and the hardness and yield strength are the highest at 530 °C, which are 275 HV and 873 MPa. The plasticity increases first and then decreases, and the plasticity is the best at 580 °C. The elongation and reduction of area were 22.87% and 71.41%. These changes in mechanical properties are mainly related to the content of martensite and reversed austenite in the microstructure. The tensile strength and elongation of SMSS under different process conditions were compared. The results show that when the quenching temperature is 930 °C and the tempering temperature is 580 °C, the comprehensive performance of SMSS is the best, reaching 18700 MPa•%. This value is 31% higher than that of forgings. Finally, the formation mechanism of reversed austenite was discussed, and the strengthening model of SMSS 00Cr13Ni5Mo was established.

AbstractAcute respiratory distress syndrome (ARDS) is a complication of pulmonary disease that produces life-threatening hypoxaemia. Despite ventilation and hyperoxic therapies, undetected hypoxia can manifest in capillary beds leading to multi-organ failure. Ox66™ is an ingestible, solid-state form of oxygen designed to supplement oxygen deficits. Twenty-four anaesthetized rats underwent a two-hit model of respiratory distress (ARDS), where a single dose (5 mg/kg) of lipopolysaccharide (LPS) was given intratracheally, and then the respiratory tidal volume was reduced by 40%. After 60 min, animals were randomized to receive Ox66™, or normal saline (NS; vehicle control) via gavage or supplemental inspired oxygen (40% FiO2). A second gavage was administered at 120 min. Cardiovascular function and blood oximetry/chemistry were measured alongside the peripheral spinotrapezius muscle’s interstitial oxygenation (PISFO2). ARDS reduced mean arterial pressure (MAP) and PISFO2 compared to baseline (BL) for all treatment groups. Treatment with Ox66 or NS did not improve MAP, but 40% FiO2 caused a rapid return to BL. PISFO2 improved after treatment with Ox66™ and 40% FiO2 and remained elevated for both groups against NS until study conclusion. Both oxygen treatments also suppressed the inflammatory response to LPS, suggesting that Ox66™ can deliver therapeutically-impactful levels of oxygen in situations of pulmonary dysfunction.

Ru-Co 3 O 4 /CoN-L electrode with abundant anion defects (V N and V O) and Ru dopants was proposed for the first time by utilizing the 'gas phase nitridation-quenching Ru' strategy. Surprisingly, thanks to the structure of twisted nanoneedles, abundant Ru dopants and anion defects, the Ru-Co 3 O 4 /CoN/NF-L exhibits exceptional HER and OER properties beyond notal-metals. [Display omitted] The difficulty of nitride modification is to develop simple and efficient strategies to induce defects and efficiently capture Ru atoms. With these in mind, this work innovatively constructed a Ru-Co 3 O 4 /CoN-L catalyst with abundant anion defects (oxygen vacancies (V O) and nitrogen vacancies (V N)) using the nitridation-quenching-Ru doping strategy. Surprisingly, the porous structure provided more active sites, and the V N and V O were conducive to promoting the anchoring of Ru atoms. These significantly improved the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) performances of the Ru-Co 3 O 4 /CoN/NF-L catalyst. The density functional theory results showed that the anion defects optimized the hydrogen adsorption capacity of the Ru active sites for the HER. Furthermore, Ru dopants and anion defects reduced the OER energy barrier of the Co-active sites, accelerating the HER and OER kinetics. This study proposes a new concept for defect construction and nitride-structure optimization. [ABSTRACT FROM AUTHOR]

The process of glass transition during the quenching in the domain with the cold wall has been numerically simulated. We have implemented the temperature-dependent form of the previously proposed theoretical model, which combined the heat transfer in the domain and the gauge theory of glass transition, assuming the presence of topologically stable distortions (disclinations) in the forming solid. The competition between crystallization (formation of polycrystalline structure) and the formation of the amorphous disordered phase has been shown. At the relatively slow cooling rates corresponding to the formation of the crystalline phase, we observed a columnar to equiaxed transition qualitatively similar to the observed in many metallic alloys. The moving front followed the equilibrium isotherm corresponding to the equilibrium temperature of transition in the disclinations subsystem, although front drag resulted in the effect of kinetic undercooling and the emergence of the maximum velocity of the crystallization front. High thermal conductivity values associated with the substantial heat flux lead to the bulk amorphous state. The dynamics of the coarsening of the primary amorphous structure depended on the annealing temperature.

The API K55 grade steel is widely utilized in seamless pipes for oil and gas exploration, especially as casing pipes for wellbores. Traditionally, this steel is processed using hot rolling followed by quenching and tempering to achieve the desired dimensional and microstructural characteristics, balancing high strength with ductility. This article introduces an alternative method to attaining the required tensile properties for API K55 grade steel by employing a biphasic microstructure (ferrite/martensite) achieved through quenching post‐intercritical austenitizing heat treatment to high‐strength‐low‐alloy steel. Thermodynamic simulations and dilatometric experiments revealed that increasing the austenitizing temperature enhances austenite formation, decreasing significantly its carbon content, which facilitates martensitic transformation and increases the Ms and Mf temperatures. A complete phase transformation mapping was presented, highlighting how the austenitizing temperature influences martensitic transformation kinetics during the quenching heat treatment. It was concluded that austenitizing at 750 °C, followed by quenching and short tempering at 650 °C, produced a biphasic microstructure with 30% ferrite and 70% martensite, providing a favorable balance between mechanical strength and ductility that meets the API K55 grade requirements, surpassing traditional methods in the industry. [ABSTRACT FROM AUTHOR]

The martensitic transformations in Cu–38Zn and Cu–39.5Zn (wt %) alloys with the shape memory effect have been studied using a combination of transmission and scanning electron microscopy, optical metallography, and X-ray diffraction analysis. When examining specimen upon cooling to low temperatures in the transmission electron microscope column, the features of martensite morphology and fine structure, as well as of electron microdiffraction in the alloys, have been ascetained. The structural types of martensite phases (3R) and (2H) have been identified in Cu–38Zn alloys, as well as (9R) and (2H), in Cu–39.5Zn alloys. The proposed crystallographic models of martensitic rearrangement in the alloys are based on an analysis of X-ray and electron diffraction, including diffuse electron scattering, as well as on the packing defects of the internal substructure of martensite. [ABSTRACT FROM AUTHOR]

The effect of heat treatment on the structural evolution, phase transformation, and mechanical strength of Al–12Si obtained using wire electron beam additive manufacturing has been investigated. The as-built Al–12Si alloy was characterized by structural inhomogeneities in the form of interlayer bands with coarsened Si particles resulted from cyclic reheating of the solidified metal. Quenching the as-built samples resulted in the increase of the volume fraction of Al/Si eutectics by 9% with simultaneous refinement of Fe-containing particles. This structure allows obtaining the combination of strength and plasticity better than that of the asbuilt sample. Annealing leads to coarsening of both Si and Fe-containing particles, thereby increasing the Al/Si volume fraction and impairing the mechanical characteristics. [ABSTRACT FROM AUTHOR]

When a suitable balance of hardness, strength, and toughness is required in civil engineering and construction, wear-resistant medium carbon steels are frequently utilized. The ability to resist plastic deformation brought on by stress or abrasion is measured by hardness. High hardness materials are typically more brittle and prone to fracture but also stronger and more resistant to corrosion. A double-quenching procedure was used in the current investigation and contrasted with the traditional single-quenching process. Additionally, a variety of cooling media are used during quenching treatments. The results demonstrate that distilled water is the most effective cooling medium to cool the models in the heat treatment of medium carbon steels because it is free of salts, suspended particles, and metal contaminants. The results show that the hardness increased following the first quenching and tempering by 37.5% above the hardness value predicted by the original model, and it increased once more following the second quenching and tempering by 10% over the hardness value following the first heat-treatment. The previous austenite grain limits and the high-angle beam limits are the main factors that give a share in to the increased hardness, and the main elements that affect how effectively they function are the high slip transmission factor and the high spacing angle between slip levels. [ABSTRACT FROM AUTHOR]

In this paper, enhancing the tribological characteristics of novel cast metallic materials—hybrid multi-component cast irons—by applying a strengthening heat treatment is described. The experimental materials were the cast alloys of a nominal composition (5 wt.% W, 5 wt.% Mo, 5 wt.% V, 10 wt.% Cr, 2.5 wt.% Ti, Fe is a balance) supplemented with 0.3–1.1 wt.% C and 1.5–2.5 wt.% B (total of nine alloys). The heat treatment was oil-quenching followed by 200 °C tempering. The quench temperature (QT) varied in the range of 900–1200 °C, with a step of 50 °C (with a 2-h holding at QT). The correlation of the QT with microstructure and properties was estimated using microstructure/worn surface characterization, differential scanning calorimetry, hardness measurement, and three-body-abrasive wear testing (using Al2O3 particles). The as-cast alloys had a multi-phase structure consisting of primary and/or eutectic borocarbide M2(B,C)5, carboborides M(C,B), M7(C,B)3, M3(C,B), and the matrix (ferrite, martensite, pearlite/bainite) in different combinations and volume fractions. Generally, the increase in the quenching temperature resulted in a gradual increase in hardness (maximally to 66–67 HRC) and a decrease in the wear rate in most alloys. This was due to the change in the phase-structure state of the alloys under quenching, namely, the secondary carboboride precipitation, and replacing ferrite and pearlite/bainite with martensite. The wear rate was found to be inversely proportional to bulk hardness. The maximum wear resistance was attributed to QT = 1150–1200 °C, when the wear rate of the alloys was lowered by three to six times as compared to the as-cast state. With the QT increase, the difference in the wear rate of the alloys decreased by three times. The highest abrasive resistance was attributed to the alloys with 1.1 wt.% C, which had a 2.36–3.20 times lower wear rate as compared with that of the reference alloy (13 wt.% Cr cast iron, hardness of 66 HRC). The effects of carbon and boron on hardness and wear behavior are analyzed using the regression models developed according to the factorial design procedure. The wear mechanisms are discussed based on worn surface characterization. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Engineering (17264073) is the property of Republic of Iraq Ministry of Higher Education & Scientific Research (MOHESR) and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Bearing is the property of Bearing Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of China Mining Magazine is the property of China Mining Magazine Co., Ltd. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

A single-photon avalanche diode (SPAD) is a photon-counting sensor renowned for its exceptional single-photon sensitivity. One significant feature of SPADs is their non-linear response to light, making them ideal for high-dynamic range imaging applications. In SPAD imaging, the photon detection mode, which depends on the quenching method employed, is crucial for optimizing image quality and dynamic range. This paper examines the free-running and gating imaging modes, evaluating their impacts on photon capture and saturation limits. Given that the number of incident photons follows a Poisson distribution, we introduce an innovative imaging-quenching model based on statistical mathematics. We designed and fabricated two SPAD imaging sensors using 180 nm CMOS technology. Image processing and evaluation were conducted using a mapping method. Our results show that in low-light conditions, the gating mode surpasses the free-running mode in the signal-to-noise ratio (SNR). However, the free-running mode exhibits a saturation limit of more than an order of magnitude higher than that of the gating mode, demonstrating its superior capability to handle a broader range of light intensities. This paper provides a thorough analysis of the differences between the two imaging methods, incorporating the theoretical mathematical model, circuit characteristics, and computed imaging quality. [ABSTRACT FROM AUTHOR]

The process of glass transition during the quenching in the domain with the cold wall has been numerically simulated. We have implemented the temperature-dependent form of the previously proposed theoretical model, which combined the heat transfer in the domain and the gauge theory of glass transition, assuming the presence of topologically stable distortions (disclinations) in the forming solid. The competition between crystallization (formation of polycrystalline structure) and the formation of the amorphous disordered phase has been shown. At the relatively slow cooling rates corresponding to the formation of the crystalline phase, we observed a columnar to equiaxed transition qualitatively similar to the observed in many metallic alloys. The moving front followed the equilibrium isotherm corresponding to the equilibrium temperature of transition in the disclinations subsystem, although front drag resulted in the effect of kinetic undercooling and the emergence of the maximum velocity of the crystallization front. High thermal conductivity values associated with the substantial heat flux lead to the bulk amorphous state. The dynamics of the coarsening of the primary amorphous structure depended on the annealing temperature. [ABSTRACT FROM AUTHOR]

The low-carbon steel revealed the presence of ferrite-pearlite and ferrite-martensite microstructures after being subjected to different thermomechanical routes. These routes involved two distinct stages: 1) reheating hot-rolled steel at 1473 K, followed by cooling via step quenching, intermediate quenching, and furnace cooling, and 2) cold rolling and subsequently annealing at 873 K for 2 and 8 h. The quenching schedules finally developed a ferrite-martensite structure with different martensitic morphology, whereas furnace cooling promotes a ferrite-pearlite structure. The prolonged annealing assists in carbide precipitation from deformed ferrite-martensite microstructure while pre-existing carbides coarsen after 8 h of annealing in furnace-cooled specimens. The sudden phase disintegration contributes to the changes in the recrystallized kinetics and evolution of precipitates, tailoring the final grain size. Additionally, the development of textures after cold rolling and annealing is studied through the emergence of α and γ fiber in BCC phase. Finally, detailed microscopic technique has been employed to correlate the overall tensile response of the investigated samples with their interrelated microstructures. [ABSTRACT FROM AUTHOR]

This paper addresses the combustion of ammonium perchlorate (AP) near adiabatic conditions at high pressures and higher initial temperatures. The AP pellets were coated with a thin layer of silica grease to simulate the near adiabatic condition. The experiments were performed at initial temperatures of 30 and 70 °C in the pressure range of 2.5–30 MPa for coated and bare pellets. The bare pellets were found to exhibit mesa burning as reported in the literature. However, the coated pellets did not exhibit mesa burning. The burn rates of coated AP pellets increased linearly for the entire pressure range of 2.5–30 MPa with 0.64 pressure index. Further, the experiments were carried out for the first time at an initial temperature of 90 °C for 14–30 MPa pressure range, wherein, AP combustion did not display any characteristics of mesa burning (pressure index of 0.33). The surface morphology of quenched samples of both bare and coated pellets of AP were studied, by quenching (rapid depressurization technique) pellets at 6, 12, and 18 MPa pressures. The surface structure of quenched samples for near adiabatic conditions was similar for all three pressures. However, for bare pellets the changes in surface structure were observed with change in pressure, similar to the literature. Mesa burning was found to be an effect of convective heat loss from the periphery of the pellets and it was not observed when heat loss was reduced or initial temperature was higher than the critical initial temperature. [ABSTRACT FROM AUTHOR]

Self‐healing materials that integrate excellent mechanical properties and high healing efficiency meet the requirements of flexible electronic sensors for mechanical flexibility and reliability. In the field of wearable devices, they are of great significance for improving the stability of the equipment and reducing the frequency of replacement. However, the high strength of materials often limits their self‐healing ability. When damage occurs, it will hinder the microstructural adjustment and fluidity of the material at the damaged site, thus negatively affecting the activation and execution of the self‐healing mechanism. In this study, a strength‐toughness and room‐temperature self‐healing triboelectric material is prepared by the dynamic nanoconfinement effect and the quenching effect of ethanol (referred to as the DNCQ strategy). The quenching effect of ethanol improves the aggregation of nanocluster phase, and the constructed nanoconfined network skillfully balances the contradiction between mechanical properties and self‐healing ability. The obtained triboelectric material has high tensile strength (27.1 MPa), toughness (97.9 MJ m−3), and excellent healing efficiency (88.6%). The self‐powered pressure distribution sensing array based on triboelectric materials can accurately reflect the pressure distribution of the object, which has potential application prospects in the field of wearable devices. [ABSTRACT FROM AUTHOR]

CsPbX 3 (X = Cl/Br, Br, Br/I, I) perovskite quantum dots (QDs) glasses have enormous application potential in the field of long wavelength pass (short wavelength cutoff) filters. In this work, the CsPbX 3 (X = Cl/Br, Br, Br/I, I) QDs doped with Se4+ were prepared in the borogermanate glass matrix. To quench strong exciton emission of QDs, the CsPbX 3 (X = Cl/Br, Br, Br/I, I) perovskite QDs glasses were doped with Se4+ at different concentrations of 0, 0.05 %, 0.1 % and 0.2 %, respectively. The nanocrystal structure, transmittance, optical density, photoluminescence (PL), PL excitation and PL decay have been investigated. The working wavelength of filters has been extended to wide range from 440 nm to 650 nm. The samples have large optical density in cutoff region, excellent steepness in the transition region, and high transmittance in transmission region. As Se4+ concentration increases, the PL intensity is quenched and the PL lifetime is decreased obviously for CsPbX 3 QDs glasses, whereas the absorption and transmittance characteristics for filters are less affected. The quenching mechanism is attributed to nonradiative recombination by deep energy level traps. The Se4+ doped CsPbX 3 QDs glasses can meet requirements for the long wavelength pass filters. [ABSTRACT FROM AUTHOR]

The process of transition from the liquid to the solid state during the uniform quenching is described by a combination of two theoretical approaches: the phase field method and the gauge theory, which suggests the phase transition in the subsystem of topologically stable distortions. Using the stochastic partial differential equations we numerically simulate competition between the processes of crystallization and vitrification during the rapid cooling of the melt. A glass order parameter which is suitable for the characterization of transition to the glassy state has been proposed. At low cooling rates, the domain freezes into the crystalline structure with defects, and its glass order parameter is orders of magnitude less than that for the vitrified state obtained by rapid quenching. Proposed method improves and extends the theoretical description of glass transition, qualitatively represents the basic kinetic properties of the process and demonstrates sensitivity of resulting microstructures to the quenching rate. [ABSTRACT FROM AUTHOR]

Initially, a brief historical review related to the discovery of iron is made. Studies of artifacts such as tools blades and weapons from more than 1000 years BC, allowed us to conclude that the knowledge already existed to increase the hardness of metals, both due to the increase in carbon content and sudden cooling from high temperatures (a process called tempering or hardening). This suggests that there was a considerable degree of sophistication on the part of these early blacksmiths. Next, the basics of materials theory and formation of the crystalline structure of iron- carbide iron (Fe-Fe3C) based on the phase diagram are presented. Modernly, materials science has shown that increasing temperature changes the atomic structure of ferrite (pure iron with BCC structure) to austenite (FCC), which allows the inclusion of other elements, such as carbon, for example. The quenching process, on the other hand, abruptly changes the atomic structure from austenite to martensite (BCT), keeping the carbon attached to the final structure, giving the new material a significant increase in hardness. Although the context of the article is, at first glance, historical, the controlled heat treatment of steel is essential for the modern world and is used to ensure that it has the desired properties in industry in general. [ABSTRACT FROM AUTHOR]

Sodium bismuth titanate‐based materials are expected to be an alternative candidate to lead‐based ceramic materials due to their excellent electrical properties. However, the low depolarization temperature (Td) limits their practical application. In this work, the phase structure evolution and microstructure of 0.9(0.4Na1/2Bi1/2TiO3–0.6BiFeO3)–0.1BaTiO3: xZnO (x = 0.01, 0.03, 0.05, and 0.07) (abbreviated as 100xZnO) composite ceramics are investigated, and their piezoelectric properties are improved by combination of constructing 0–3 type composites and quenching treatment technology. The addition of ZnO can increase both Td and d33 because ZnO can enhance the lattice distortion of rhombohedral phase and lead to the increase in ferroelectric order. Specifically, the optimum composition x = 0.03 obtains the d33 value of 106 pC/N (25°C), which retains 84% of the value at room temperature up to 240°C. And the quenching technology further enhances the ferroelectric order and increases Td, which is up to 280°C for x = 0.03. [ABSTRACT FROM AUTHOR]

Solid solution strengthened ferritic ductile iron proves to have a better ratio of tensile strength to elongation than conventional ductile iron grades. This applies up to a maximum silicon content of 4.3 wt%, beyond which it leads to an abrupt decrease in ultimate tensile strength and elongation at fracture. During solidification of high silicon ductile iron, negative segregation of silicon occurs, and the highest silicon concentration is observed near the graphite nodules. This high silicon concentration leads to long-range ordering of iron and silicon, and this ordering results in formation of superstructures like BCC_B2 and D03. The presence of super structures restricts the mobility of dislocations and leads to abrupt fracture of the material. This research focuses on the investigation of silicon homogenization by the addition of aluminium and heat treatments to avoid the formation of brittle iron–silicon superstructure. Thermodynamic–kinetic simulations as well as experimental investigations, including variation in alloy composition and quenching, are performed. The results provide a promising understanding to control the micro-segregation of silicon in ductile cast iron based on heat treatments and alloy composition. [ABSTRACT FROM AUTHOR]

Biochar is one of the most important carbon-rich minerals with a porous structure in the carbon sequestration, immobilization of metal and organic contaminants, as well as soil fertility improvement. However, its large-scale use is very limited in the agriculture and environment, due to the high cost of production and transportation from agricultural biowaste to plant. In this study, a new technology was explored to directly convert from agricultural biowaste to biochar in the field. The local applications had significantly reduced the costs of biochar. Inspired by nature, biochar production was also proposed in the field, where only agricultural biowaste, water, and fire were required for biomass carbonization and charcoal formation; Specifically, Litchi branches sourced from subtropical regions were utilized as feedstock to explore an on-site production of biochar. Soil (Ferralsols) slurry was applied as a coating and quenching agent to create an oxygen-limited environment during fire-water coupled carbonization of the feedstock. This self-limiting oxidation approach was used to minimize the expenses of production, transportation, and utilization. Biochar that was produced with soil slurry coating and quenching also displayed the highest carbon content (83.5%) and carbon capture capacity (83.9%), exceeding unconverted biomass and biochar produced without coating by 16.7% and 37.8%, respectively. The burning process of Litchi branches was divided into three stages: 1) Surface was charred immediately but with an unburned core; 2) Surface was grayed out, while the core was in a self-ignition state with high temperature and limited oxygen, and the dark red char fell to the ground; and 3) The dark red char gradually burned out to be ash. Spraying water on the dark red char was used to prevent the occurrence of the 3rd stage, thus favoring the formation of biochar instead of ash. Furthermore, the soil coating likely acted as a barrier, thus reducing carbon monoxide or carbon dioxide release during combustion. Additionally, the soil integration was facilitated to form the mineral-carbon composite for the carbon capture. Scanning electron microscopy and energy spectroscopy analysis show that the regular structure of the carbon skeleton was observed after coating and quenching the iron-aluminum slurry. The iron-aluminum minerals were also loaded on the surface. A novel approach to carbonization accelerated a paradigm shift in biochar production from a sophisticated stationary facility to a simple way for practical use in the field. Low cost greatly contributed to the agricultural and environmental application of biochar. The economically viable combination of fire and soil (Ferralsols) slurry coupled carbonization can be expected to provide valuable insights for biochar adoption and carbon neutrality. In conclusion, the readily available agricultural residues and soil-based coatings can be integrated to mitigate the environmental impact of biochar production, in order to enhance the efficacy as a carbon capture. These findings can offer significant implications for the broader adoption of biochar as a sustainable solution, in order to promote climate and soil health. [ABSTRACT FROM AUTHOR]

Copyright of Iron Steel Vanadium Titanium is the property of Iron Steel Vanadium Titanium Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Methods of transmission and scanning electron microscopy are used to study premartenstic states and their relation to martensitic transformations in the alloys Cu–38 wt % Zn and Cu–39.5 wt % Zn with shape memory effect. Analysis of the observed diffusion scattering of electrons is carried out, including in situ experiments at heating and cooling and the defect condition of the internal substructure of austenite and martensite. The crystallographic models of martensitic transitions β2 → , β2 → , and β2 → are proposed based on the crystallographic data obtained in the premartensitic state. [ABSTRACT FROM AUTHOR]

In this study, an environmentally sustainable fluorimetric method for determination of Vonoprazan fumarate (VON) in dosage forms using nanoprobes consisting of nitrogen and sulfur co‐doped carbon quantum dots (N, S‐CQDs). The N, S‐CQDs were prepared through a microwave‐assisted method in 30 s. The resulting N, S‐CQDs were characterized using transmission electron microscopy (TEM), high‐resolution transmission electron microscopy (HRTEM), Fourier transform infrared spectroscopy (FTIR), and X‐ray photoelectron spectroscopy (XPS). They exhibit fluorescence emission at 460 nm after excitation at 385 nm with a high quantum yield (60%). The analytical approach for VON determination relies on the quenching effect exerted by VON on the native fluorescence intensity of CQDs. The quenching mechanism was investigated using Stern–Volmer plots. The proposed method demonstrates linearity across a concentration range 10–80 μM (4.6–36.8 μg/mL) with corresponding limits of detection and quantitation calculated as 2.17 μM (0.99 μg/mL) and 6.58 μM (3.02 μg/mL), respectively. The method has been effectively utilized for the determination of VON in the pharmaceutical samples. Statistical comparison with reported RP‐HPLC has been performed to verify the accuracy and precision of the developed method. The environmental sustainability of the developed method has been thoroughly examined through various greenness metrics. [ABSTRACT FROM AUTHOR]

Mefenamic acid, renowned for its analgesic properties, stands as a reliable choice for alleviating mild to moderate pain. However, its versatility extends beyond pain relief, with ongoing research unveiling its promising therapeutic potential across diverse domains. A straightforward, environmentally friendly, and sensitive spectrofluorometric technique has been developed for the precise quantification of the analgesic medication, mefenamic acid. This method relies on the immediate reduction of fluorescence emitted by a probe upon interaction with varying concentrations of the drug. The fluorescent probe utilized, N‐phenyl‐1‐naphthylamine (NPNA), was synthesized in a single step, and the fluorescence intensities were measured at 480 nm using synchronous fluorescence spectroscopy with a wavelength difference of 200 nm. Temperature variations and lifetime studies indicated that the quenching process was static. The calibration curve exhibited linearity within the concentration range of 0.50–9.00 μg/mL, with a detection limit of 60.00 ng/mL. Various experimental parameters affecting the quenching process were meticulously examined and optimized. The proposed technique was successfully applied to determine mefenamic acid in pharmaceutical formulations, plasma, and urine, yielding excellent recoveries ranging from 98% to 100.5%. The greenness of the developed method was evaluated using three metrics: the Analytical Eco‐scale, AGREE, and the Green Analytical Procedure Index. [ABSTRACT FROM AUTHOR]