Search

The influences of CO2 incorporated in gas nanobubbles (NBs) on palm oil crystallisation and physical characteristics were investigated. Initially, CO2 NB-treated palm oil had a significantly (p ≤ 0.05) larger amount of dissolved CO2 (~ 1200–1700 ppm). The crystal morphology evaluation showed smaller size and higher number of palm oil crystals by the presence of CO2 NBs. Additionally, the attendance of NBs caused a slight increment in crystallising enthalpy magnitude and a significant reduction in final end-set melting temperatures (by 4.5–6 °C) of palm oil stored at 4 °C. There was also a significant (p ≤ 0.05) increase in melting enthalpies by 1.3–3.5 J/g and 6.5–9 J/g of the NB-treated samples under 48-h storage conditions at 23 °C and 4 °C, respectively. Furthermore, the CO2 NB-treated palm oil was characterised by both lighter colour and lower hardness. Research findings demonstrate that the introduction of food-grade gas NBs can be a sustainable and eco-friendly method to tailor thermal behaviour and physical properties of palm oil. [ABSTRACT FROM AUTHOR]

Microcrystalline cast stone is a silicate inorganic nonmetallic material prepared via a melting–casting–crystallization process using slag as the main raw material and appropriate nucleating, quenching, and tempering agents. However, crystallization of the microcrystalline cast stone causes overall shrinkage, producing defects such as holes on the surface and inside and affecting the quality and yield. In this work, the effect of quartz-sand addition on the formation of voids in microcrystalline cast stone prepared from blast-furnace slag is studied. The theoretical composition, phase transformation, and microstructure of microcrystalline cast stone are analyzed through FactSage thermodynamic calculations, X-ray diffraction, and scanning electron microscopy. The results show that the main crystal phases in the microcrystalline cast stone are gehlenite and akermanite for 5, 7, 8, and 10 % quartz-sand addition. When the amount of quartz sand added is 8 %, the overall shrinkage rate of the ordinary augite phase is 16 %. The maximum amount of dicalcium silicate is formed, filling the holes on the surface and inside and inhibiting the formation of holes. The crystal morphology is snowflake-like and the crystal connections are dense. The flexural strength reaches a maximum value of 40.08 MPa, which improves the overall performance of the microcrystalline cast stone. The results of this study can provide technical support for improving the yield and quality of microcrystalline cast stone prepared by melting. [Display omitted] [ABSTRACT FROM AUTHOR]

The morphology of calcium oxalate monohydrate precipitates (COM, Ca(C2O4)·H2O, P21/c, whewellite) occurring as crystals or intergrowths, as well as distribution of crystal‐bearing idioblasts, have been studied for the first time in the bark of stone birch Betula ermanii from Sakhalin Island sampled in an area affected by mud volcanism and an unaffected typical forest environment taken for reference. The study addresses several issues (i) number and size of phytoliths and their distribution in different cell types; (ii) density of calcification in specific cells; (iii) habits of single crystals, twins, and complex intergrowths, as well as frequency of different morphologies and their relations. The trends of time‐dependent morphological changes in separately analyzed crystals and intergrowths record the evolution of COM morphology from nuclei to mature grains. Of special interest are the nucleation sites and features of organic and inorganic seeds and nuclei for COM phytoliths. The precipitation process and crystal habits are mainly controlled by supersaturation, and it is thus important to constrain the Ca distribution patterns in different bark tissues. The B. ermanii samples were analyzed by several methods: scanning electron microscopy (SEM) for the distribution patterns and micromorphology of COM precipitates and bulk Ca content in bark; electron probe microanalysis (EPMA) for the mineral chemistry of COM precipitates; inductively coupled plasma optical emission spectrometry (ICP‐OES) and inductively coupled plasma mass spectrometry (ICP‐MS) for trace elements in bulk bark and wood. Research Highlights: The distribution and morphology of whewellite precipitates in the analyzed B. ermanii bark samples indicate that the aqueous solution was most strongly supersaturated with respect to the Ca(C2O4)·H2O solid phase at the parenchyma‐sclerenchyma boundary, where most of the COM spherulites are localized and often coexist with large single crystals and contact COM twins. [ABSTRACT FROM AUTHOR]

Semicrystalline polyamides (PAs) are optimal materials to develop high-pressure resistant liners for type IV hydrogen storage tanks due to a favorable combination of barrier performance, mechanical resistance, and lightness. However, experimental data on hydrogen transport in PAs are incomplete or inconsistent, and usually do not report separately the contributions of solubility and diffusivity, hence limiting a deep understanding of the permeation mechanism and its dependence on the material structure. Moreover, recent developments have led to the design of modified polyamides which could better serve the high-pressure storage applications. In this work, the hydrogen barrier performance of Polyamide 6 (PA6), Polyamide 11 (PA11) and an impact-modified PA 6 (PA6-I), was evaluated and the results obtained with different techniques and on different samples compared. Permeation measurements were performed in constant-volume and constant-pressure apparatuses at different temperatures and pressures, on different samples of each material. Sorption measurements were carried out into a differential sorption system. Results from the permeation and sorption devices were compared against each other and with literature data, allowing to understand the effect of various factors. The H 2 solubility in PA is mostly affected by density, as a lower free volume of the amorphous phase leads to a lower gas uptake. On the other hand, diffusivity and, consequently, permeability, are also strongly affected by the morphology of the crystal phase, which depends on the production protocol. In most of the cases inspected, the discrepancy between data from different experimental techniques or literature works can be explained by the different crystal morphology of the samples used in the test. Temperature enhances diffusivity, permeability and solubility, while the pressure reduces the permeability, as it lowers the free volume, and increases the activation energy of permeation. An estimation of the minimum thickness required to meet high-pressure storage technical guidelines was provided for the case of PA6-I. • H 2 sorption and transport in commercial polyamides (PA6, PA6I, and PA11) was tested. • Three techniques were compared: sorption, permeation and high-pressure permeation. • Different temperatures up to 80 °C and pressures up to 700 bar were studied. • Experimental data are in agreement and differences were properly motivated. • PA6 is the best material and a minimum thickness to meet EU 406/2010 was determined. [ABSTRACT FROM AUTHOR]

Cerium dioxide (CeO 2) supported palladium (Pd) catalysts have found widespread application in CO oxidation reaction owing to their exceptional catalytic performance. The morphology of the CeO 2 support dictates the exposed crystal plane, exerting a profound influence on surface structure and redox properties. This is crucial as the atomic arrangement at the surface directly impacts catalytic activity. In this study, a range of CeO 2 supports with diverse morphologies (e.g. nano-octahedra, nano-cubes, nano-particles, nano-spheres, and nano-rods) were successfully synthesized through hydrothermal methods and subsequently supported with Pd for CO oxidation. The spherical 1Pd/CeO 2 –S catalyst, revealing exposed (111) + (100) crystal planes, exhibited significantly higher CO catalytic oxidation activity compared to the catalysts with other morphological CeO 2 supports. The results indicated a positive correlation between the content of Pd x Ce 1-x O 2-y species and catalytic activity. Notably, this species was most abundantly formed in the spherical 1Pd/CeO 2 –S catalyst with exposed (111) + (100) crystal planes. The presence of this active species facilitated the formation of surface defects, increased oxygen vacancy concentration, and enhanced metal-support interaction, consequently greatly improving the CO low-temperature catalytic oxidation activity. Consequently, the oxidation state of Pd in the Pd/CeO 2 catalyst could be effectively regulated by controlling the exposure of (111) + (100) crystalline surfaces of the CeO 2 support, further optimizing the catalytic performance of the Pd/CeO 2 catalytic system. [ABSTRACT FROM AUTHOR]

Copyright of Shipin Kexue/ Food Science is the property of Food Science Editorial Department 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.)

CALF-20, [Zn2(1,2,4-triazolate)2(oxalate)] shows remarkable performance in post-combustion carbon capture, even under humid conditions1 but its reported crystal morphology hinders its applicability in mixed matrix membranes (MMMs). Here, a route to its preparation as platelets a few tens of nm thick is reported. These were incorporated into a PEBAX MH1567 polymer matrix and the resultant MMMs display improvement in CO2 permeability and CO2/N2 selectivity. [ABSTRACT FROM AUTHOR]

This research involved synthesizing In 2 S 3 –In(OH) 3 nanosheets through a simple hydrothermal method at a low reaction temperature. The impact of different indium chloride concentrations on the morphology and crystal structure of In 2 S 3 –In(OH) 3 nanostructures was investigated. The discussion extended to the photocatalytic hydrogen evolution of both In 2 S 3 –In(OH) 3 nanosheets and nanofibers. These findings indicated that In 2 S 3 –In(OH) 3 nanofibers exhibited optimal photocatalytic hydrogen production at various indium chloride concentrations. Furthermore, In 2 S 3 –In(OH) 3 –ZnS heterostructures were created by reacting In 2 S 3 –In(OH) 3 nanosheets with varying concentrations of ZnS precursors. The study delved into the morphology and crystal structure, emphasizing photocatalytic hydrogen production in In 2 S 3 –In(OH) 3 –ZnS nanofibers under different concentrations of ZnS precursors. Remarkably, the In 2 S 3 –In(OH) 3 –ZnS nanofibers demonstrated exceptional hydrogen production efficiency, attributed to their larger specific surface area, improved blue light absorption, and reduced electron-hole pair recombination. Additionally, a comprehensive analysis explored the photocatalytic reaction mechanism, pH values, sacrificial reagents, sacrificial reagent concentrations, light source types, and intensities. These results highlighted the exceptional reusability of In 2 S 3 –In(OH) 3 –ZnS nanofibers in photocatalytic hydrogen production, showcasing their potential for cost-effective and highly efficient applications in diverse fields. [Display omitted] • Synthesized In 2 S 3 –In(OH) 3 nanosheets using a simple hydrothermal method. • Explored photocatalytic hydrogen evolution in nanosheets and nanofibers. • In 2 S 3 –In(OH) 3 –ZnS nanofibers demonstrated exceptional hydrogen production efficiency. • Analyzed photocatalytic reaction mechanism, pH values, sacrificial reagents, and light sources. • Demonstrated high reusability and efficiency potential for various applications. [ABSTRACT FROM AUTHOR]

Using citric acid as a chelating agent, BiFeO3 nanopowders doped with La at the A-site, Mn at the B-site, and codoped with La/Mn were synthesized through an ultrasonic-assisted sol-gel method. Characterization techniques such as X-ray diffraction (XRD), ultraviolet visible diffuse reflectance spectroscopy (UV-DRS), X-ray photoelectron spectroscopy (XPS), specific surface area and pore size analysis (BET), and photoluminescence spectroscopy (PL) were employed to analyze the morphology, structure and elemental composition of Bi1 - x Lax Fe1 - y Mny O3 crystals. The results indicate that doping with La and Mn elements can significantly alter the crystal structure and morphology of BiFeO3, suppressing the recombination of its charge carriers. Using Bi1 - x Lax Fe1 - y Mny O3 as a photocatalyst, the effects of pH value and light source on the photocatalytic degradation of simulated pollutants were investigated, and further experiments to explore the photocatalytic mechanism were conducted. The results reveal that La/Mn co-doped samples show significant differences in degradation rates for congo red (CR) and methylene blue (MB), which is related to the electronegativity of the dye molecules. Meanwhile, doping enhances the magnetic properties of the samples, which is beneficial for recycling and improving its utilization efficiency. [ABSTRACT FROM AUTHOR]

Morphology‐controlled Cs2SbBr6 crystals are synthesized by Bi‐ and Ag‐substitution of the precursor solution. X‐ray diffraction (XRD) together with Raman spectroscopy confirms the lattice tilting and symmetry changes with the dominant appearance of higher index facets by Bi substitution. Ag substitution does not induce crystal symmetry changes in the Cs2BBr6 (B = Sb or Bi) phase, but results in highly defective structures hindering the formation of a smooth surface during the crystal growth. Successful substitution of Bi and limited substitution of Ag into Cs2SbBr6 is also confirmed by energy dispersive X‐ray spectroscopy (EDX). This research provides design principles and practical examples of how to control the morphology of Cs2SbBr6 crystals with structural defects and multiphase formation. [ABSTRACT FROM AUTHOR]

Here, a morphologically based approach is used for the in situ characterization of 3D growth rates of facetted crystals from the solution phase. Crystal images of single crystals of the β‐form of l‐glutamic acid are captured in situ during their growth at a relative supersaturation of 1.05 using transmission optical microscopy. The crystal growth rates estimated for both the {101} capping and {021} prismatic faces through image processing are consistent with those determined using reflection light mode [Jiang, Ma, Hazlehurst, Ilett, Jackson, Hogg & Roberts (2024). Cryst. Growth Des.24, 3277–3288]. The growth rate in the {010} face is, for the first time, estimated from the shadow widths of the {021} prismatic faces and found to be typically about half that of the {021} prismatic faces. Analysis of the 3D shape during growth reveals that the initial needle‐like crystal morphology develops during the growth process to become more tabular, associated with the Zingg factor evolving from 2.9 to 1.7 (>1). The change in relative solution supersaturation during the growth process is estimated from calculations of the crystal volume, offering an alternative approach to determine this dynamically from visual observations. [ABSTRACT FROM AUTHOR]

Slow‐cooled CF8M duplex stainless steel is used for critical parts of the primary coolant pipes of nuclear reactors. This steel can endure severe service conditions, but it tends to become more brittle upon very long‐term aging (tens of years). Therefore, it is essential to understand its specific microstructure and temporal evolution. As revealed by electron backscatter diffraction (EBSD) analyses, the microstructure consists of millimetre‐scale ferritic grains within which austenite lath packets have grown with preferred crystallographic orientations concerning the parent ferritic phase far from the ferrite grain boundaries. In these lath packets where the austenite phase is nucleated, the lath morphology and crystal orientation accommodate the two ferrite orientations. Globally, the Pitsch orientation relationship appears to display the best agreement with the experimental data compared with other classical relationships. The austenite lath packets are parallel plate‐shaped laths, characterized by their normal n. A novel methodology is introduced to elucidate the expected relationship between n and the crystallographic orientation given the coarse interfaces, even though n is only partly known from the observation surface, in contrast to the 3D crystal orientations measured by EBSD. The distribution of retrieved normals n is shown to be concentrated over a set of discrete orientations. Assuming that the ferrite and austenite obey the Pitsch orientation relationship, the determined lath normals are close to an invariant direction of the parent phase given by the same orientation relationship. [ABSTRACT FROM AUTHOR]

The composition, thermal properties, and microstructure of some mutton tallows (MTs), such as sheep tallow (ST), goat tallow (GT), and sheep tail tallow (STT), were investigated and compared with those of beef tallow (BT). The results showed that the fatty acids (FAs) in the MTs were dominated by oleic, stearic, and palmitic acids, which were similar to those of BTs; also there were some natural trans and odd‐carbon FAs occurred in these tallows. Comparison with STs, GTs, and BTs, STT had higher triunsaturated and diunsaturated‐monosaturated triacylglycerols (TAGs) and lower monounsaturated‐disaturated and trisaturated TAGs. Solid fat content (SFC) profile of STT was different those of STs, GTs, and BTs, whereas STs, GTs, and BTs had similar SFC profiles. In the range of 0–50°C, STT had a lower SFC compared with STs, GTs, and BTs at a given temperature. DSC results showed that MTs had melting and crystallization curves similar to BTs; and the GT, ST, and BT had higher melting and crystallization temperatures than STT. All MT and BTs crystals are β′ form; there also exists certain β form. The microscopic morphology of the STT was radial spherical aggregates, and those of other MT and BTs were consisted of radial inner core and low density outer halo area. Practical Application: The results of SFC, microstructure, and morphology indicated mutton tallows containing the desired crystal form and crystal morphology could be used as shortening base fats. The research can provide a theoretical basis for expanding the application of mutton tallows in food industry. [ABSTRACT FROM AUTHOR]

Molten salt synthesis (MSS) represents an emerging green and environmentally friendly approach for engineering the structural and phase characteristics of multifunctional materials. In this study, we report the rapid synthesis of cobalt (Co)-based electrodes through MSS under 15 min with high yield. Our findings reveal that the selection of salt precursor significantly influences the crystal phase and morphology of the Co-based electrodes as well as the electrochemical properties. Hydroxide-based salts yielded layered NaxCoO2 with a thin hexagonal morphology, while nitrate-based salts resulted in spinel phase Co3O4 with octahedral structures. Our proposed mechanism highlights the critical role of ionic bonding in these phenomena. The electrochemical evaluation demonstrates that the layered NaxCoO2 electrodes exhibit a specific capacitance of 59 F g−1 (47.2 C g−1) at 1 A g−1 and excellent long-term capacity retention. On the other hand, spinel Co3O4 electrodes, when employed as oxygen evolution reaction (OER) catalysts, exhibit an overpotential of 341 mV to drive a current density of 10 mA cm−2, which is comparable to Co3O4 prepared using other methods that required a significant amount of synthesis time. [ABSTRACT FROM AUTHOR]

The synthesis of Cu2O nanoparticles (NPs) through the reduction of copper hydroxide using ascorbic acid and then Cu2O NPs modified with triacetoxy(vinyl)silane (TVAS) (m-Cu2O) by solution method were achieved. FTIR analysis of the unmodified Cu2O NPs and m-Cu2O NPs revealed the presence of absorption characteristics corresponding to Cu–O–Si linkages in the FTIR spectra of m-Cu2O NPs, which is strong evidence that the Cu2O NPs have been successfully modified. The characteristics and properties of m-Cu2O NPs were determined and compared to those of the u-Cu2O NPs. The results indicated that the modification process had an insignificant effect on the crystal structure and morphology of Cu2O NPs. X-ray diffraction analysis indicated that the crystal grain size of m-Cu2O NPs slightly increased, measuring 41.04 nm compared to 38.36 nm for the u-Cu2O NPs, this change was minor. However, the m-Cu2O NPs demonstrated enhanced dispersion into acrylic emulsion polymer, resulting in improved abrasion resistance and thermal stability of the acrylic coating. In comparison with an acrylic coating filled with the u-Cu2O NPs, the coating filled with m-Cu2O NPs exhibited a 70% increase in abrasion resistance and better thermal stability. Importantly, the antibacterial performance against E. coli and S. aureus of acrylic coating filled with m-Cu2O NPs was similar to that of the u-Cu2O NPs nanocomposite coating. These findings underscore the versatility and benefits of chemical modification in enhancing specific properties of the acrylic coating without compromising antibacterial efficacy. [ABSTRACT FROM AUTHOR]

In this work, the effects of deposition potential and the surface preparation, such as the cathodic activation and the sandblasting on the nucleation and growth of zinc-nickel alloy from acidic aqueous solution containing 0.47 and 0.56 M of zinc ions and nicke ions l respectively in presence of additives were studied. The zinc-nickel were deposited on as-machined and sandblasted substrates not activated or activated at 0, 50 and 150 A dm−2. The Scharifker–Hills and Palomar-Pardavé models were used to analyse the potentiostatic current-transient curves, and revealed that the nucleation of zinc–nickel remains instantaneous with a typical three-dimensional growth process, no matter the surface preparation. However, the characteristics and the features of zinc–nickel alloys coatings are vastly modified, in particular the morphology and the crystal structure, although the crystallized phase (the cubic γ-phase) remains identical. However, the preferential growth varies according to the sandblast process and thus the roughness of the substrate, which implies different crystallite size and adhesion of the coating on the substrate. [ABSTRACT FROM AUTHOR]

Nonuniform cementation challenges may arise when employing microbially induced calcium carbonate precipitation (MICP) technology to treat problematic soils. Electrokinetic methods exhibit the potential to regulate the MICP process by driving negatively charged urease-producing bacteria and promoting the migration of reactant ions. However, the current understanding of bacterial behavior and the characteristics of CaCO3 precipitates under the influence of direct current (DC) electric fields remains unclear. In this study, we designed and fabricated microfluidic chips to simulate sandy soil matrices. By monitoring the real-time MICP reaction process in the microfluidic porous medium with and without a DC electric field through an optical microscope, we analyzed the impact of the electric field on the behavior of bacteria at different locations (i.e., attached and suspended bacteria) and on the morphology and distribution of CaCO3 crystals. Results show that initially injected bacteria adhered to the inner pore surfaces due to interfacial cohesion, whereas subsequently injected bacteria were predominantly suspended in the pore solution and driven toward the anode by the electric field, where they aggregated. Furthermore, the majority of Ca2+ precipitated near the cathode, resulting in larger-sized crystals, and a smaller quantity of Ca2+ precipitated at the anode, generating smaller-sized crystal particles. This observation highlights the crucial role of Ca2+ movement in determining the distribution of CaCO3. Under the influence of a DC electric field, the final precipitated CaCO3 crystals exhibit nonuniform sizes, with an overall smaller average size and more complex crystal morphologies. Our results provide the underlying insights to guide the regulation of the MICP process through applied electric fields. [ABSTRACT FROM AUTHOR]

The solubility of nicotinohydrazide in two binary solvents were determined by a static weight method from 293.15 to 318.15 K. It found that the solubility of nicotinohydrazide was influenced by temperature, solvent polarity, and solvent composition. Meanwhile, the TG-DSC analysis was used to obtain the weight change and thermal effect of nicotinohydrazide. The XRD analysis indicated that the crystal morphology of nicotinohydrazide was coincident in five different solvents. Furthermore, the models including modified Apelblat equation, Van't Hoff equation, Jouyban-Acree model, and CNIBS/R-K model were used to fit the experimental data. It was concluded that the four models were reliable in fitting the experimental data. Then the dissolution apparent thermodynamic was obtained, which explained well the dissolution of nicotinohydrazide. This study could help optimize and control the industrial crystallization of nicotinohydrazide. [ABSTRACT FROM AUTHOR]

Transparent SrAl 2 O 4 :Eu2+,Dy3+ glass-ceramics with significant mechanoluminescence (ML) have been prepared by the melt quenching method. Phase composition and crystal morphology of the glass-ceramics have been studied. X-ray diffraction (XRD) and scanning electron microscopy (SEM) tests indicate that SrAl 2 O 4 crystals in the glass matrix have an oriented growth characteristic influenced by the doping Dy3+ ions. Meanwhile, more Dy3+ ions doping results in refined grain structures and a more ordered arrangement of crystals. Photoluminescence (PL) spectra show that as the concentration of Dy3+ ions increases, the luminescence intensity of the glass-ceramics decreases, but long persistent luminescence (LPL) enhances. The emission peaks at 522 nm attributed to 4 f65d1→4 f7 transitions, arise from the combined luminescence effect of Eu2+ ions in both crystal and glass phases. Further investigation indicates that the as-prepared glass-ceramics exhibit significant mechanoluminescence (ML), which can last for a relatively long duration. [Display omitted] • Transparent SrAl 2 O 4 :Eu2+,Dy3+ glass-ceramics were prepared. • SrAl 2 O 4 crystal grains have a certain crystallographic orientation in the glass matrix. • Dy3+ ions can refine the crystallization. • The luminescence of glass-ceramics is combined luminescence effect of Eu2+ ions in both crystal and glass phases. • SrAl 2 O 4 glass-ceramics have a significant mechanoluminescence. [ABSTRACT FROM AUTHOR]

The effects of soluble ions on the morphology and crystal growth of calcium sulfate hemihydrate whiskers are very significant. In order to gain a deeper understanding of the basic theory of regulating whiskers, this paper summarises the progress of research on the effects of different types and concentrations of soluble cations in desulfurization gypsum on the whisker preparation. The low concentration of Na+ has a small effect on the calcium sulfate hemihydrate whiskers and barely affects the morphology and surface smoothness of the whiskers. The content of K+ is suitable to be 3% (mass fraction) or below, and the higher content has a detrimental effect on the growth of calcium sulfate hemihydrate whiskers. Mg2+ makes the whisker surface more homogeneous and crystalline. And the trace amount of selective adsorption of Al3+ has no effect on the whisker length-to-diameter ratio. Similar to K+, Fe3+ also has the optimal concentration, which is lower than 2 mmol / L. Unlike the cations mentioned above, Cu2+ is not from the raw material, but is an additional ion introduced in the doping of the appropriate amount of Cu2+ is conducive to the formation of whiskers with a smooth and uniform surface. [ABSTRACT FROM AUTHOR]

Phreatic overgrowths on speleothems (POS) are unique precipitates that are found in a small number of coastal caves around the world, like those in the Mallorca Island. Their growth is directly related to the water level of the brackish lakes connected to the sea characteristic of these caves and, therefore, they can be very reliable indicators of past sea levels. The study presented here characterizes and classifies an important number of POS samples collected in the coastal caves of Mallorca. The characterization includes not only the observations made on 117 handheld samples and on 102 thin sections from POS, but also the study of their mineralogy and their location in the caves. This study has provided the basis for a systematization of all these characteristics, some of which are reported here for the first time in POS samples. The results indicate that (1) most of the POS precipitate on stalactites, (2) calcite POS show branched internal and external texture and their most common crystal fabric is mosaic calcite and (3) aragonite POS show globular external texture and fan‐shaped internal texture, and their principal crystal fabric is needle‐like. All the aragonitic samples have been found above or at the same heights as the current sea level, which indicates that they have probably formed during warmer climates. The calcite POS have been found at heights above and below the present sea level and are interpreted as to have formed during cold and rainy periods. The systematization proposed in this paper could be applied and checked in other POS worldwide. Additionally, the combination of these results with the information obtained from studies on the present precipitation of these phreatic speleothems in some Mallorca caves has provided an insight on their formation conditions which will enlarge the utility of these speleothems as palaeoenvironmental indicators. [ABSTRACT FROM AUTHOR]

Manganese dioxide with high theoretical capacity has drawn a great deal of attention for aqueous zinc‐ion batteries (ZIBs). Nevertheless, their sluggish diffusion kinetics, low electrical conductivity and limited active sites are still hindering the potential application in batteries. Herein, amorphous MnO2 nanosheets with abundant oxygen vacancies are facilely prepared by using carboxymethylcellulose sodium (CMC) as a capping agent. During the growth process, CMC can preferentially attach to the (003) facet of MnO2 to guide its crystal growth and morphology. The small nanosheets can expose abundant edge sites, along with the surface oxygen vacancies, to facilitate the insertion/extraction of H+ and Zn2+ in ZIBs. Moreover, the presence of CMC can stabilize the Mn3+ to inhibit the Jahn–Teller effect in the preparation process. As a result, CMC‐MnO2 based ZIB can provide a specific capacity of 324 mAh g−1 at 0.5 A g−1, and achieve 86.2% retention after a long cycle test of 1000 cycles. Furthermore, the energy storage mechanism may be attributed to the insertion/extraction of H+/Zn2+, dissolution/deposition of MnO2 and Zn4SO4(OH)6·nH2O, and irreversible transformation of vermiculite during long cycles. This work may open new perspectives for the development of MnO2‐based cathodes in ZIBs. [ABSTRACT FROM AUTHOR]

The cation exchange reaction is a powerful method for generating nanomaterials with unique structures because of the easy control of the size, morphology, composition, and crystal structure of the nanoparticles. This study investigated the kinetically controlled morphology and composition of colloidal nanoparticles (NPs) through cation exchange reactions, specifically focusing on variations from copper sulfide to transition metal sulfides, including Co, Fe, Zn, and Mn sulfides. In the cation exchange reaction, Co exhibited the fastest exchange rate, followed by Fe,Mn, and Zn. The difference in kinetics rates affected the change in morphology; Co, with the fastest rate, was immediately and uniformly distributed in the NPs. For Fe, a sandwich structure was initially formed and this gradually transformed into a solid-solution phase. After exchanging Cu with Mn and Zn, a heterostructure was formed, which became increasingly clear as the reaction progressed. The transformation of the morphology and crystal structure were confirmed using XRD, TEM, and SEM analyses. The findings of this study suggest that the morphology and distinct structures of the exchanged particles can be controlled by manipulating the kinetics rates of cations through cation exchange reactions. This process offers a powerful tool for the tailored synthesis of colloidal nanoparticles and provides a design principle for enabling predictable outcomes through cation exchange reactions. [ABSTRACT FROM AUTHOR]

In this manuscript, a simple one-pot heat-up method has been used to prepare multi-component copper-tin-sulfur nanomaterials, including binary Cu1.94S, ternary Cu4SnS4, and Cu1.94S/Cu4SnS4 nanocrystals by varying the reaction temperature, reaction time, and the type of copper source. Post-synthetic ligand exchange (LE) has further been introduced to replace the long-chain ligands originating from 1-dodecanethiol. It has been found that the LE process not only changes the surface ligands but also significantly affects the crystal structure and optical properties of nanocrystals. After LE, the crystal structures of Cu1.94S and Cu4SnS4 transformed to Cu7S4 and Cu3SnS4, respectively, with the Cu1.94S/Cu4SnS4 nanocrystals showing the same trend. This phenomenon could be ascribed to the loss of Cu+ originating from the strong complexation of Cu+ and ammonia with the formation of [Cu(NH3)n]2+ ions under aerobic conditions. Proton nuclear magnetic resonance (1H NMR) has been used to characterize the ligands on the surface before and after LE, which further demonstrated that the -SH was replaced during LE. Meanwhile, the band gaps of the obtained nanocrystals after LE show an obvious shift in the near-infrared region due to the evolution of crystal structures. This study will provide useful guidance for the LE of nanocrystals and the application of copper-based sulfide nanomaterials in optoelectronics and other fields. [ABSTRACT FROM AUTHOR]

In this study, we have investigated the effect of strontium (Sr) doping on the thermoelectric properties of thin films made of tin telluride (SnTe). The preparation of Sn 1-x Sr x Te (x = 0, 0.1, 0.2, 0.3, 0.4) films using a straightforward thermal evaporation method and subjected them to post-annealing at 773 K. The surface morphology and crystal structure of the films have been examined by using SEM and XRD, respectively. Our findings indicate that the Seebeck coefficient value increased from 39 to 68 μV/K as the Sr doping concentration increased. This enhancement has been attributed to the energy filtering effect resulting from charge carrier dislocation. However, the electrical conductivity value decreased due to an increase in defect density. The maximum enhancement of the power factor has been observed for x = 0.3, where the value reached 38.9 μWcm−1K−2, which is greater than the pristine sample. Our results conclude that Sr 0.3 doping in Sn 0.7 Te is a valuable addition for thermoelectric applications at room temperature. Additionally, the use of the simple thermal evaporation method for film preparation highlights its potential for large-scale applications. [ABSTRACT FROM AUTHOR]

The conventional solid-phase sintering method for the preparation of Ln 2 Ti 2 O 7 ceramics using oxides as reactants generally requires higher temperature, larger pressure, and greater energy consumption. In this paper, we synthesize a Eu 2 Ti 2 O 7 ceramic powder in relatively low-temperature molten salt (KCl–NaCl) using Eu 2 O 3 powder and TiO 2 powder as reactants at 1000 °C. The results of XRD, SEM, and element mapping indicate that the product have high phase purity, good crystal morphology and uniform chemical composition. Moreover, Eu 2 Ti 2 O 7 -based glass-ceramics are obtained by sintering with different contents of borosilicate glass. The SEM images of glass-ceramic show that almost no obvious defects or voids are found on the surface of the samples. The values of water absorption for all glass-ceramic waste forms are less than 0.5 %. With the increase of ceramic embedding rate, the hardness of the glass-ceramics first increases and then decreases, while the density gradually increases. When the embedding rate increased to 30 wt%, the hardness of glass-ceramic reaches a maximum of 19.53 GPa. The glass-ceramic waste form embedded with 30 wt% Eu 2 Ti 2 O 7 exhibits very stable chemical durability with a low leaching rate of 1.42 × 10−8 g m−2 d−1 at 90 °C even after 28 days. [ABSTRACT FROM AUTHOR]

Vapor‐deposited inverted perovskite solar cells utilizing self‐assembled monolayer (SAM) as hole transport material have gained significant attention for their high efficiencies and compatibility with silicon/perovskite monolithic tandem devices. However, as a small molecule, the SAM layer suffers low thermal tolerance in comparison with other metal oxide or polymers, rendering poor efficiency in solar device with high‐temperature (> 160 °C) fabricating procedures. In this study, a dual modification approach involving AlOx and F‐doped phenyltrimethylammonium bromide (F‐PTABr) layers is introduced to enhance the buried interface. The AlOx dielectric layer improves the interface contact and prevents the upward diffusion of SAM molecules during the vapor–solid reaction at 170 °C, while the F‐PTABr layer regulates crystal growth and reduces the interfacial defects. As a result, the AlOx/F‐PTABr‐treated perovskite film exhibits a homogeneous, pinhole‐free morphology with improved crystal quality compared to the control films. This leads to a champion power conversion efficiency of 21.53% for the inverted perovskite solar cells. Moreover, the encapsulated devices maintained 90% of the initial efficiency after 600 h of ageing at 85 °C in air, demonstrating promising potential for silicon/perovskite tandem application. [ABSTRACT FROM AUTHOR]

Hypothesis: The physical and mechanical properties of triacylglycerols (TAGs), or 'fats', depend on their composition and thermal history which, in turn, impact crystal structure and morphology. We examine whether thermal history can be mechanistically related to film removal by a surfactant solution. Experiments: Model TAG mixtures, comprising triolein:tripalmitin:tristearin 0.5:0.3:0.2, were subjected to a range of cooling profiles from the melt (0.5-80 °C/min, Newtonian and annealed), and the resulting solid films characterised by microscopy, X-ray diffraction, infrared spectroscopy, and contact angle measurements. Film removal from a model glass substrate by an aqueous surfactant solution of sodium dodecylsulphate and dodecyldimethylamine oxide at room temperature fixed at 25 °C was examined under quiescent flow conditions. Findings: Quantitative relations are established between TAG cooling profile, crystal structure and morphology, surface energy γ S F E , and removal (or 'cleaning'). In general, films cooled slowly from the melt yield heterogeneous morphologies with predominantly β 1 ′ phase, higher polar γ S F E , and faster removal timescales. By contrast, rapid cooling results in homogeneous films, rich in β 2 ′ phase, low polar γ S F E , and long removal times. Our results elucidate the non-trivial impact of TAG thermal history, connecting the multiscale semi-crystalline structure to surface energy, and eventually to film delamination by micellar solutions. [ABSTRACT FROM AUTHOR]

Copyright of Shipin Kexue/ Food Science is the property of Food Science Editorial Department 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.)

Highly efficient off‐diagonal THz generators based on novel organic nonlinear optical single crystals with optimal polar axis orientation in the as‐grown crystal morphology are introduced. The newly developed fluorinated and non‐fluorinated cationic chromophores exhibit a non‐centrosymmetric crystal structure with P21 space group symmetry in the crystalline phase. In particular, PB5FB‐T (5‐fluoro‐2‐(4‐(2‐(hydroxymethyl)pyrrolidin‐1‐yl)styryl)‐3‐methylbenzothiazol‐3‐ium 4‐methylbenzenesulfonate) crystals have an in‐plane polar axis, along with a top‐level off‐diagonal component of the nonresonant effective first hyperpolarizability of ≈100 × 10−30 esu. This stands in stark contrast to previously reported organic THz crystals, which either show a small off‐diagonal optical nonlinearity with an in‐plane polar axis or a large off‐diagonal optical nonlinearity with an almost out‐of‐plane polar axis. Employing an off‐diagonal THz generation configuration, PB5FB‐T crystals generate a THz electric field approximately four times higher than previously reported benchmark analogous crystals with a polar axis nearly out‐of‐plane. Moreover, PB5FB‐T crystals yield smooth THz spectral shapes without significant absorption dimples up to 6 THz when utilizing 130‐fs pump pulses at the wavelength of 1300 nm. [ABSTRACT FROM AUTHOR]

Highlights In this paper, the reasons for the improved wear resistance of irradiation‐modified Polytetrafluoroethylene (RM‐PTFE) and its composites above the melting point were investigated from the microcrystalline point of view by using methods such as crystallization kinetics, and it was found that the linear wear rate of RM‐PTFE was only 0.3 um/km, with a 1000 times increase in wear resistance, which was due to the transformation of its crystals from flake crystals that were easily dislodged to spherical crystals that were more resistant to abrasion. It was also found that the linear wear rate of Polytetrafluoroethylene (PTFE) with coke and graphite was 0.2 and 0.1 μm/km, respectively, and the abrasion resistance was further improved, which was attributed to the lowering of spherical crystal grain size by coke and graphite, which had better mechanical properties. These studies lay the foundation for future research on the frictional wear mechanism of RM‐PTFE above the melting point. Irradiation‐modified PTFE above the melting point Wear resistance of PTFE increases 1000 times Changes in crystal morphology dramatically increase wear resistance Use of crystallization kinetics to study the crystalline form of PTFE Small grain size improves wear resistance [ABSTRACT FROM AUTHOR]

Chloride–ion batteries (CIBs) offer a compelling alternative to conventional battery systems, particularly in applications demanding cost‐effectiveness and resource sustainability. However, the development of tailored electrode materials remains a critical bottleneck for CIB advancement. In this study, an untapped class of perovskite‐based material, potassium hexachlorostannate (K2SnCl6, denoted as KSC) is synthesized via a facile mechanochemical route for the first time. The prepared KSC is subjected to various characterization techniques to confirm its crystal structure and morphology. Herein, KSC exhibits intriguing electrochemical performance in a non‐aqueous CIB configuration, utilizing a lithium metal counter electrode. Furthermore, ex situ X‐ray diffraction (XRD) and X‐ray photoelectron spectroscopy (XPS) analysis, reveal a conversion reaction mechanism involving chloride ion shuttling and provide insights into structural evolution during cycling. Moreover, the density functional theory (DFT) studies support additional degradation products that can potentially limit the performance of these materials as potential battery electrodes in CIBs. [ABSTRACT FROM AUTHOR]

Magnesium metal batteries (MMBs), recognized as promising contenders for post‐lithium battery technologies, face challenges such as uneven magnesium (Mg) plating and stripping behaviors, leading to uncontrollable dendrite growth and irreversible structural damage. Herein, we have developed a Mg foil featuring prominently exposed (002) facets and an architecture of nanosheet arrays (termed (002)‐Mg), created through a one‐step acid etching method. Specifically, the prominent exposure of Mg (002) facets, known for their inherently low surface and adsorption energies with Mg atoms, not only facilitates smooth nucleation and dense deposition but also significantly mitigates side reactions on the Mg anode. Moreover, the nanosheet arrays on the surface evenly distribute the electric field and Mg ion flux, enhancing Mg ion transfer kinetics. As a result, the fabricated (002)‐Mg electrodes exhibit unprecedented long‐cycle performance, lasting over 6000 h (>8 months) at a current density of 3 mA cm−2 for a capacity of 3 mAh cm−2. Furthermore, the corresponding pouch cells equipped with various electrolytes and cathodes demonstrate remarkable capacity and cycling stability, highlighting the superior electrochemical compatibility of the (002)‐Mg electrode. This study provides new insights into the advancement of durable MMBs by modifying the crystal structure and morphology of Mg. [ABSTRACT FROM AUTHOR]

Calcium oxalate (CaOx) urolithiasis is a prevalent urinary disorder with significant clinical impact. This study investigates the therapeutic potential of Morin Hydrate (MH), a natural bioflavonoid, in preventing CaOx stone formation. Molecular docking studies revealed that MH binds strongly to glycolate oxidase (GO), suggesting its inhibitory effect on oxalate synthesis. In vitro assays demonstrated that MH effectively inhibits CaOx crystal nucleation, aggregation, and growth, altering crystal morphology to less stable forms. Diuretic activity studies in Wistar rats showed that MH substantially increased urine volume and ion excretion, indicating its moderate diuretic effect. In vivo experiments further supported these findings, with MH treatment improving urinary and serum markers, reducing oxidative stress, and protecting renal tissue, as evidenced by histopathological analysis. Notably, MH administration significantly decreased GO and lactate dehydrogenase activities in urolithiatic rats, indicating a reduction in oxalate production. These results suggest that MH is a promising candidate for the prevention and treatment of CaOx urolithiasis, with the potential for clinical application in reducing the risk and recurrence of kidney stones. [ABSTRACT FROM AUTHOR]

ABSTRACT Saddle dolomite is a Ca–Mg carbonate characterized by curved crystal faces, curved cleavage and sweeping extinction under cross‐polarized light. Saddle dolomite and, generally, Ca–Mg carbonates with curved crystal faces, are often assigned to the burial (hydrothermal) realm and serve as proxy archives for hydrogeochemical processes in sedimentary basins and orogens. At present, the physicochemical conditions leading to the formation of these peculiar warped carbonates are unclear, and the mechanisms inducing the curvature of their crystal lattice are debated. This study uses laboratory experiments to assess the factors controlling the formation of carbonates with curved crystal faces as a function of fluid temperature, reactant size, fluid salinity and fluid Mg : Ca. Results show that a range of magnesium calcites with curved surfaces form at elevated temperatures (ca 220°C) from calcium‐rich fluids (Mg : Ca = 0.43) within a wide range of fluid salinities (5 to 40 wt.%). Magnesium calcites that nucleate epitaxially on rhombohedral or saddle dolomite substrates exhibit warped surfaces, while those that nucleate on calcite seeds form flat surfaces. Although the two crystal habits can co‐occur, Mg‐calcites with curved crystal faces (Mg : Ca of 0.35 to 0.40) tend to be more calcium‐rich than those with flat faces (Mg : Ca of 0.58 to 0.74). In experiments with higher fluid temperature (230°C), calcite reactants undergo replacement by dolomite exhibiting planar crystal faces. The results collectively indicate that the formation of Ca–Mg carbonates with warped surfaces is likely related to a combination of geochemical and physical parameters and various threshold limits, as opposed to one specific parameter, for example, elevated fluid temperature, as is commonly reported in the literature. Although most of the present experimental precipitates are disordered magnesian calcites with bent crystal faces, it is reasonable, at the level of a tentative working hypothesis, that these represent precursors of many ancient saddle dolomites commonly found in burial settings. [ABSTRACT FROM AUTHOR]

Hybrid single crystals (HSCs) of different poly(ε‐caprolactone) (PCL) homopolymers with a poly(ε‐caprolactone)‐b‐poly(ethylene oxide) (PCL‐b‐PEO) block copolymer (BCP) are prepared. The effects of PCL length, PCL/PCL‐b‐PEO molar ratio, crystallization temperature (Tc), and solvent on crystal morphology are investigated. The optimal Tc for the formation of more perfect HSCs is between those for homocrystals of individual PCL and PCL‐b‐PEO and roughly increases with the length of PCL and PCL/PCL‐b‐PEO molar ratio. The chain folding in the HSCs is studied by comparing the experimentally measured heights obtained by atomic force microscopy (AFM) and theoretically calculated ones based on a sandwich structure model. Under most situations, the PCL homopolymers adopt a larger chain folding number in the HSCs than that in their homocrystals, while the chain folding of BCP remains unaltered. However, when both PCL homopolymer and PCL‐b‐PEO BCP crystallize slowly and the overcrowding of the PEO is effectively alleviated, thicker HSCs can be formed, in which the PCL homopolymer preserves the chain folding in its homocrystals but the BCP adopts a reduced chain folding number as compared with that in its homocrystals. The relative crystallization rate of PCL homopolymer versus BCP also affects the real composition and overall height of the HSCs. [ABSTRACT FROM AUTHOR]

Supercapacitors require excellent cycling stability and rate capability for electrodes. The NiCo2S4 spinel structure has caught much attention for its high conductivity and high theoretical specific capacity. However, due to the lack of active sites, it has been restricted in supercapacitors. In this research, the NiCo2S4 nano-material with needle, sheet and porous network morphologies were prepared by the addition of different kinds of surfactants via a simple hydrothermal method. At 1 mA/cm2, capacitance of these NiCo2S4 nanomaterials is measured as 2.09 F/cm2, 3.22 F/cm2, and 4.42 F/cm2, respectively. It was found that the exposure ratio of (111) and (220) crystal facets also has an effect on electrochemical performance, and NiCo2S4 with I (1 1 1) /I (2 2 0) of 3:1 showed better performance. Furthermore, NiCo2S4-PN//AC asymmetrical supercapacitor was assembled with NiCo2S4-PN serving as positive electrode and activated carbon (AC) as negative electrode. At a power density of 7.284 mW/cm2, energy density achieved was 0.625 mWh/cm2. Additionally, capacitance retention rate remained at 79.6% of initial capacitance after 1500 cycles. These outcomes are of great significance for developing more efficient, stable and reliable transition metal sulfide-based supercapacitors. NiCo2S4 nanomaterials with needle, sheet, and porous network morphologies with different exposure ratios of (111)/(220) crystal facets were obtained using a simple two-step hydrothermal method. The type of surfactant plays a key role in the preparation of NiCo2S4 nanomaterials. The cyclic stability and rate capability of NiCo2S4 nanomaterials were improved by increasing the ratio of exposed (111)/(220) crystal facets. [ABSTRACT FROM AUTHOR]

Polylactic acid (PLA) is currently the largest volume of production and application of synthetic biodegradable polymer via bio-derived materials. However, the relaxation characteristics and very low crystallization rate determined by the hand- structure of PLA chains result in low heat-resistance temperature and troublesome demold behavior for fast extrusion and/ or injection molding process. It is well known, by introducing of nucleating agent and crystal growing accelerator, the crystallization properties of PLA materials can be improved efficiently. In the paper, the isothermal crystallization behaviors of PLA, which include the rate and temperature of crystallization, crystallinity, crystals morphologies, were systemically shown. Meanwhile, a serious of regulation strategies of isothermal crystallization kinetics of PLA materials, such as adding of biodegradable polymers, different dimension of fillers, various chain-reconstruct for PLA, processing flow fields and post-treatment, were comprehensively summarized. Additionally, the regularity strategies and next study points for PLA isothermal crystallization behavior were also presented. [ABSTRACT FROM AUTHOR]

The proper control of perovskite crystal morphology is a fundamental aspect of achieving efficient perovskite solar cells (PSCs) by ensuring better film coverage on an electron transport layer (ETL). In this study, three distinct approaches to depositing perovskite were thoroughly examined using different measurement techniques such as X-ray diffraction, photoluminescence spectra, UV-visible spectroscopy, and scanning electron microscopy. The impact of these perovskite deposition methods performed in an air-processed condition on the power conversion efficiency (PCE) of PSCs was thoroughly investigated. The results highlight that the infiltration of a mesoporous TiO2 ETL scaffold with perovskite solution yields much better coverage when employing sequential deposition processing, as opposed to single-step deposition processing. Moreover, the performance of perovskite-based photovoltaics is significantly improved to 6.8% by employing the two-step deposition dipping approach, which actively prevents the development of disorganized capping layers. This surpasses the 5.2% efficiency achieved through the one-step deposition method. Additionally, by optimizing the thickness of the mesoporous TiO2 film and using the spin coating method for the organic precursors in the process of perovskite formation, a significant enhancement in PCE is accomplished, surpassing 13.6%. Moreover, the best performing devices without encapsulation can retain 97% of the initial PCE over 40 days, under dark, 35% relative humidity, and room temperature. Hence, in this study the ambient air fabrication capability of the sequential deposition approach is demonstrated for the efficient and stable PSCs. [ABSTRACT FROM AUTHOR]

This study focuses on the synthesis and characterization of SiO2–CaO–P2O5–Na2O nanofiber bioglass (BG) tablets using cellulose nanofibers (CNFs) as a template and starch binders. Three types of tablets are prepared: sago starch binder tablets, xanthan gum binder tablets, and dry press tablets (used as a control). The tablets are investigated for their physicochemical structure, mechanical properties, in‐vivo bioactivity, and antibacterial efficiency using various characterization techniques such as Fourier transform infrared (FTIR), field emission scanning electron microscope (FESEM), XRD, ICP, etc. The results indicate the formation of a hydroxyapatite (HA) layer on the surface of the tablets after immersion in simulated body fluid (SBF) for 28 days, demonstrating their bioactivity. FESEM analysis reveals the formation of HA crystals with different morphologies, including oval‐shaped crystals in sago tablets and needle‐like crystals in xanthan tablets. The binder tablets exhibit higher Ca/P ratios compared to the press‐dried tablets. Among the binder tablets, sago starch tablets show superior mechanical properties. Additionally, the binder tablets display efficient antibacterial activity against Staphylococcus aureus and Escherichia coli bacteria. These findings highlight their potential as promising candidates for bone tissue engineering applications. [ABSTRACT FROM AUTHOR]

Owing to the excellent optoelectronic characteristics, such as high absorption coefficient and suitable bandgap, CuPbSbS3 semiconductor materials have a wide application prospect in solar cells. In this paper, CuPbSbS3 films were deposited in the annealing process of tube furnace through butyldithiocarbamic acid (BDCA) solution method. CuPbSbS3 film is regulated deposited by adjusting the proportion of CS2 in BDCA solution. The effect of the proportion of CS2 in BDCA solution on the surface morphology and crystal structure of CuPbSbS3 films was analyzed by scanning electron microscopy and X-ray diffractometer. The results indicate that deposited CuPbSbS3 film exhibits good crystalline morphology by fixing the volume ratio of ethanol, n-butylamine, and carbon disulfide of 7. 4∶9. 6∶6. Then, solar cells with the structure of FTO/SnO2 / CuPbSbS3 / Spiro-OMeTAD/Ag were fabricated. The interfacial charge transport kinetics of CuPbSbS3 solar cells were further investigated by Mott-Schottky curves, Nyquist impedance spectra, dark current density-voltage curves, and current-voltage curves of symmetrical devices in the dark state. The results from the above electrical measurements demonstrate that the defect recombination center density and charge transport resistance of the deposited CuPbSbS3 films is effectively reduced, decreasing the non-radiative recombination of photogenerated carriers and improving the carrier transport ability. Finally, the CuPbSbS3 solar cell shows a photoelectric conversion efficiency of 0. 81% (a short-circuit current density of 9. 08 mA·cm-2 and an open-circuit voltage of 250 mV). The relevant research results provide an experimental basis for the fabrication of high-quality CuPbSbS3 films. [ABSTRACT FROM AUTHOR]

This study aims to examine the 50/50 polypropylene/polyamide 6 (iPP/PA6) system molded under confined flow conditions, both in its original state and after being modified by two different interfacial agents. This study provides two main insights. Firstly, it focuses on a polymer blend close to phase inversion. Secondly, it investigates the impact of using two different types of interfacial agents (derived from polymer waste) to enhance the compatibility between iPP and PA6. Dynamic Mechanical Analysis (DMA) has been employed to achieve these objectives. It is important to note that the investigation of the 50/50 iPP/PA6 system is a crucial focus predicted in previous studies, where a series of mechanical properties were evaluated using Box–Wilson design of experiments (DOEs) over the whole compositional range on the iPP/PA6 binary system. Thus, two interfacial modifiers, namely succinic anhydride (SA)-grafted atactic polypropylene with terminal, side, and bridge SA grafts (aPP-SASA) and succinyl-fluoresceine (SF) with bridge succinic anhydride grafting atactic polypropylene (aPP-SFSA), were employed. The authors obtained and characterized these agents. The quantity of these agents used in the blend was identified as a critical coordinate in prior studies conducted by the authors. The processing method used, compression molding under confined conditions, was chosen to minimize any orientation effect on the emerging morphology. All characterization procedures were performed on samples processed by contour machining to retain the blend morphologies as they emerged from the processing stage. Results from WAXS and SAXS synchrotron tests concluded there were no changes in the crystal morphology of the iPP or the PA6 in the blends nor any co-crystallization process throughout the compositional range. These findings, and the long period fits on the PP crystalline phase for the fifty/fifty blends we are discussing, will support the present DMA study. Finally, the efficiency of these interfacial modifiers has been concluded, even in this unfavorable scenario. [ABSTRACT FROM AUTHOR]

Herein, this study has examined the influence of Zn2+ sources during a biogenic-mediated pathway to synthesize ZnO nanoparticles with highly desirable solar-responsive catalytic properties. Salts of nitrate, acetate and chloride have been utilized. The ZnO powders underwent characterization using diverse analytical tools, including XRD, FTIR, Raman, BET, SEM, TEM with EDS/elemental mapping and UV-vis absorption/emission spectroscopic analyses. Accordingly, precursors have proved to affect crystallinity, morphology, surface characteristics, optical properties and the photocatalytic degradation of methylene blue (MB) model pollutant. It was observed that ZnO derived from zinc acetate precursor (Z-AC NPs) exhibits very fast photocatalytic degradation of MB at pH 11 with superior kinetic estimates of 0.314 min−1 and t1/2 = 2.2 min over many of recent reports. In contrast, the chloride precursor is not recommended along with the employed biogenic route. The intriguing findings could be directly correlated to the decreased crystal size, augmented surface area, the hexagonal morphology of the crystals, high potency in absorbing visible photons, high efficacy in separating photogenerated charge carriers and producing high amounts of •OH radicals. Further testing of Z-AC NPs in photocatalytic remediation of water samples from Dumat Aljandal Lake in Aljouf, Saudi Arabia, contaminated with MB and pyronine Y (PY) dyestuffs, showed high dye photodegradation. Therefore, this work could lead to an extremely fast avenue for decontaminating wastewater from hazmat dyestuff. [ABSTRACT FROM AUTHOR]

Epidermal wax is strategically situated at the interface between plants and air; therefore, it plays a key role in plants' interactions with their surroundings. It is also unstable and susceptible to light intensity. Hosta plants are shade-loving herbs with admirable flowers and leaves. Hosta 'Halcyon' and Hosta ensata F. Maek. are two species of Hosta with a glaucous and a glossy appearance, respectively. Light intensity can affect the composition of epicuticular wax on the leaf surface, which influences the leaf color phenotype and ornamental value. In this paper, the crystal micromorphology, content, and components of epicuticular wax on the leaves of two species of Hosta under different light conditions (10%-, 30%-, 50%-, 70%-, and 100%-intensity sunlight, relative light intensity (RLI)) have been studied using pot experiments. The results indicate that the epicuticular wax crystals of H. 'Halcyon' and H. ensata are tubular and platelet-like, respectively. The wax crystals of H. 'Halcyon' melted and formed a thick crust under 100% RLI, and those of H. ensata melted and formed a thick crust under 70% and 100% RLI conditions. The primary ingredients of the epicuticular wax of the two species of Hosta contained primary alcohols, alkanes, fatty acids, and esters; β-diketones were only detected in H. 'Halcyon'. The quantity of epicuticular wax of H. 'Halcyon' reduced at first and then increased with an RLI increase, achieving its lowest value at 50% RLI, but that of H. ensata declined little by little. The amounts of C28 primary alcohols, C31 alkanes, and C18 fatty acids were significantly higher than those of other carbon atoms in the two genotypes of Hosta. The C31β-diketones content decreased with the increase in light intensity, which caused the white frost phenotype to gradually weaken in H. 'Halcyon'. [ABSTRACT FROM AUTHOR]

This research was aimed to conduct solvent‐free crystallization and fractionation of virgin coconut oil (VCO). This study investigated the effect of surface contact area‐to‐volume ratio and mixing conditions on crystal characteristics. Commercially available VCO samples, extracted by different methods, were analyzed for fatty acid and triacylglycerol composition using GC–MS and UPLC–ELSD. VCO extracted through enzyme and chilling–thawing cycles exhibited higher medium chain fatty acids and medium chain triacylglycerols, which was selected for crystallization studies. Isothermal crystallization of VCO at 21°C assessed the effect of scale of crystallizer tube on cooling rate using Newton's law of cooling equation. The smaller tube (20 mm diameter) with a higher surface contact area‐to‐volume ratio produced 4.1‐fold faster cooling and a higher crystallization yield (44%) compared to the 80 mm diameter tube when no agitation was applied. Whereas mixing with a magnetic stirrer produced a large number of nuclei, generating intense crystallization heat, and rendering the crystals inseparable from liquid fraction. The process of VCO crystallization was also studied for kinetics and crystal growth mechanism using the Avrami model employing angled rotation of sample tube during non‐isothermal crystallization. Angled rotary mixing produced stable crystals and significantly increased the crystallization rate (t1/2 = 26.86 min) with polyhedral or spherulitic crystal growth (n = 3.25) compared to non‐mixing condition (t1/2 = 161.87 min) with restricted linear growth (n = 1.64). DSC analysis of VCO and its fractions obtained after crystallization using the 20 mm tube with angled rotary mixing indicated shifts in their thermogram peaks, suggesting differences in triacylglycerol compositions. Practical applications: Virgin coconut oil (VCO) is well recognized for its health‐beneficial properties, yet its application is limited due to its complex triglyceride composition. The solvent‐free crystallization method facilitates VCO fractionation into phases with different melting points without hazardous solvents. The efficacy of this process is highly dependent on temperature, cooling rate, and agitation, which affects crystal morphology and growth kinetics. This study addresses these challenges in the scarcely investigated area of VCO crystallization. The resulting fractions can be customized for specific applications based on their altered functional properties in producing baking and confectionery coatings, salad dressings, and so on. The olein fraction obtained in this study can be utilized in nutraceutical formulations targeting digestive and cognitive health, as it is reported to be rich in medium chain triglycerides. This research optimizes process conditions, suggesting an efficient method for dry‐fractionating VCO, which is significantly associated with the food and pharmaceutical industries. [ABSTRACT FROM AUTHOR]

The effect of structure of organic additives on the electrodeposition behavior of Zn from alkaline zincate solution and its crystal morphology was investigated. Zn was electrodeposited on an Fe electrode at 20-1000 A·m-2, 2.4 x 104 C·m-2, 300K from unagitated zincate solutions containing the various organic additives as a leveling agent. The suppression effect of additives on the charge transfer and diffusion of ZnO22- ions in Zn electrodeposition corresponded to the number of adsorption site per a straight chain molecule of polymer. The effect of polymer alone on the decrease in size of Zn platelets crystals was small, but the crystal size significantly decreased with coexistence of low molecular additive. The crystal size of deposited Zn decreased in spite of small suppression effect on Zn deposition, showing that the crystal size of deposited Zn doesn't depend on the overpotential for deposition. With coexistence of low molecular additive with polymer, the crystal of deposited Zn was fine regardless of kind of polymer even though Zn deposited at the diffusion control of ZnO22- ions. [ABSTRACT FROM AUTHOR]

Copyright of Chemical Engineering (China) / Huaxue Gongcheng is the property of Hualu Engineering Science & Technology 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.)

Crystallization is important to the pharmaceutical, the chemical, and the materials fields, where the morphology of crystals is one of the key factors affecting the quality of crystallization. High-throughput screening based on microfluidic droplets is a potent technique to accelerate the discovery and development of new crystal morphologies with active pharmaceutical ingredients. However, massive crystal morphologies' datum needs to be identified completely and accurately, which is time-consuming and labor-intensive. Therefore, effective morphologies' detection and small-target tracking are essential for high-efficiency experiments. In this paper, a new improved algorithm YOLOv8 (YOLO-PBESW) for detecting indomethacin crystals with different morphologies is proposed. We enhanced its capability in detecting small targets through the integration of a high-resolution feature layer P2, and the adoption of a BiFPN structure. Additionally, in this paper, adding the EMA mechanism before the P2 detection head was implemented to improve network attention towards global features. Furthermore, we utilized SimSPPF to replace SPPF to mitigate computational costs and reduce inference time. Lastly, the CIoU loss function was substituted with WIoUv3 to improve detection performance. The experimental findings indicate that the enhanced YOLOv8 model attained advancements, achieving AP metrics of 93.3%, 77.6%, 80.2%, and 99.5% for crystal wire, crystal rod, crystal sheet, and jelly-like phases, respectively. The model also achieved a precision of 85.2%, a recall of 83.8%, and an F1 score of 84.5%, with a mAP of 87.6%. In terms of computational efficiency, the model's dimensions and operational efficiency are reported as 5.46 MB, and it took 12.89 ms to process each image with a speed of 77.52 FPS. Compared with state-of-the-art lightweight small object detection models such as the FFCA-YOLO series, our proposed YOLO-PBESW model achieved improvements in detecting indomethacin crystal morphologies, particularly for crystal sheets and crystal rods. The model demonstrated AP values that exceeded L-FFCA-YOLO by 7.4% for crystal sheets and 3.9% for crystal rods, while also delivering a superior F1-score. Furthermore, YOLO-PBESW maintained a lower computational complexity, with parameters of only 11.8 GFLOPs and 2.65 M, and achieved a higher FPS. These outcomes collectively demonstrate that our method achieved a balance between precision and computational speed. [ABSTRACT FROM AUTHOR]

In this study, we investigated improving the performance of a layered double hydroxide (LDH) for the adsorption of As(III) and As(V) by controlling the morphology of LDH crystals. The LDH was synthesized via a simple coprecipitation method using barely soluble MgO as a precursor and succinic acid (SA) as a morphological control agent. Doping the LDH crystals with carboxylate ions (RCOO−) derived from SA caused the crystals to develop in a radial direction. This changed the pore characteristics and increased the density of active surface sites. Subsequently, SA/MgFe-LDH showed excellent affinity for As(III) and As(V) with maximum sorption densities of 2.42 and 1.60 mmol/g, respectively. By comparison, the pristine MgFe-LDH had sorption capacities of 1.56 and 1.31 mmol/g for As(III) and As(V), respectively. The LDH was effective over a wide pH range for As(III) adsorption (pH 3–8.5) and As(V) adsorption (pH 3–6.5). Using a combination of spectroscopy and sorption modeling calculations, the main sorption mechanism of As(III) and As(V) on SA/MgFe-LDH was identified as inner-sphere complexation via ligand exchange with hydroxyl group (–OH) and RCOO−. Specifically, bidentate As-Fe complexes were proposed for both As(III) and As(V) uptake, with the magnitude of formation varying with the initial As concentration. Importantly, the As-laden adsorbent had satisfactory stability in simulated real landfill leachate. These findings demonstrate that SA/MgFe-LDH exhibits considerable potential for remediation of As-contaminated water. [Display omitted] [ABSTRACT FROM AUTHOR]