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Myrrh has unique medicinal properties: it is an anti-inflammatory, antifungal, and antibacterial material. The aim of this study was to assess the influence of ethanolic myrrh extract on the production and properties of modified PP and PLA melt spun yarns. In this work, multifilament yarns of polylactide (PLA) and polypropylene (PP) containing 10 wt% myrrh resin at different melt-spinning drawing ratios (DRs) were prepared. The results of scanning electron microscopy revealed that the multifilament yarns from polymers covered by myrrh resin extract had a smooth surface without cracks or visible myrrh derivatives. The influence of myrrh resin on the mechanical properties of PP and PLA multifilament yarns was analyzed, and it was found that the presence of myrrh (PP/M, PLA/M) increased tenacity (cN/tex) and decreased the tensile strain (%) of melt spun yarns obtained at different draw ratios (DRs). During optical analysis, it was found that the absorbance of yarns increased in the entire UV region of the spectra, which was most likely determined by the presence of myrrh. The degree of crystallinity and the wetting angle of PP/M and PLA/M multifilament yarns increased compared with the pure PLA and PP multifilament yarns. This study concludes that the presence of myrrh derivatives influences PLA yarns degradation rate and antibacterial effects against Gram-positive bacteria. [ABSTRACT FROM AUTHOR]

Secondary ion mass spectrometry (SIMS) is often used to determine the sulfur contents and isotope ratios of metallic alloys in meteorites or high‐pressure experimental samples. However, SIMS analyses involve calibration and the determination of instrumental mass fractionation in reference materials with a matrix composition similar to that of the unknown samples. To provide metallic reference materials adapted to S measurements via SIMS, we synthesised a series of twenty‐eight alloys comprising four FeNi(±Si) compositions (Fe95Ni5, Fe90Ni10, Fe80Ni20, and Fe80Ni15Si5) with S contents varying from 100 μg g−1 to 4 g/100g using the "melt spinning" method, which guarantees that the metal alloys are rapidly quenched at ~ 106 K s−1. Sulfur contents were determined at the Service d'Analyse des Roches et Minéraux at the CRPG and absolute δ34S values were determined by multi‐collector ICP‐MS (MC‐ICP‐MS, ThermoScientific Neptune) and isotope ratio mass spectrometry (Thermoscientific Delta V). A δ34S value of 16.01 ± 0.31‰ was consistently obtained using the MC‐ICP‐MS, which was indistinguishable of the δ34S value of the FeS starting material (15.95 ± 0.08‰). It suggests that S did not undergo isotopic fractionation during the melting process. Of fifteen samples containing ≤ 5000 μg g−1 S, SIMS measurements with 15‐μm‐diameter spots were repeatable to within 10% relative (1 standard deviation, 1s) for S contents and 2‰ for δ34S values. However, samples containing > 5000 μg g−1 S showed FeNi–FeS immiscibility, leading to minor dispersion of the S mass fractions and δ34S values. No matrix effect was observed for Fe‐Ni, Si, or S contents in terms of the calibration curves and instrumental mass fractionation. We ultimately recommend eight samples as reliable reference materials for S isotopic measurements by SIMS, which we can share worldwide with other laboratories. [ABSTRACT FROM AUTHOR]

Fiber lithium‐ion batteries (FLIBs) hold great promise for powering wearable electronics. However, their practical application is hindered by limited cycle and calendar life, primarily due to the loss of active Li caused by water vapor permeation through the encapsulation layer. To address this challenge, a low‐permeability and high‐flexibility tetrafluoroethylene hexafluoropropylene copolymer (FEP) tube is presented to continuously encapsulate FLIBs by melting extrusion method. Owing to the inherent hydrophobicity of fluorine resins and appropriate crystallinity of the polymer matrix, FEP tubes exhibited significantly low vapor permeability, with a water vapor transmittance rate (WVTR) of 0.3 mg·day−1·pkg−1, 15 times lower than that of the nylon 12 tubes (4.6 mg·day−1·pkg−1). Leveraging the low permeability and elastic modulus of FEP tubes, FLIBs demonstrate a capacity retention of 80.05% after 180 cycles and exceptional flexibility with a capacity retention of 98.32% after 10 000 bending cycles, showcasing superior performance compared to the conventional polymer tubes (for example, the capacity of PP‐FLIBs declined by 20.68% after 30 cycles). This work presents a general and efficient strategy for continuously encapsulating FLIBs, effectively extending their cycle and calendar lifetime of FLIBs, thereby enhancing their practical viability for wearable electronic applications. [ABSTRACT FROM AUTHOR]

Effectively identifying and preventing anomalies in the melt process significantly enhances production efficiency and product quality in industrial manufacturing. Consequently, this paper proposes a study on a melt anomaly identification system for pelletizers using autoencoder technology. It discusses the challenges of detecting anomalies in the melt extrusion process of polyester pelletizers, focusing on the limitations of manual monitoring and traditional image detection methods. This paper proposes a system based on autoencoders that demonstrates effectiveness in detecting and differentiating various melt anomaly states through deep learning. By randomly altering the brightness and rotation angle of images in each training round, the training samples are augmented, thereby enhancing the system's robustness against changes in environmental light intensity. Experimental results indicate that the system proposed has good melt anomaly detection efficiency and generalization performance and has effectively differentiated degrees of melt anomalies. This study emphasizes the potential of autoencoders in industrial applications and suggests directions for future research. [ABSTRACT FROM AUTHOR]

Most single-screw extruders used in the plastics processing industry are plasticizing extruders, designed to melt solid pellets or powders within the screw channel during processing. In many cases, the efficiency of the melting process acts as the primary throughput-limiting factor. If the material melts too late in the process, it may not be sufficiently mixed, resulting in substandard product quality. Accurate prediction of the melting process is therefore essential for efficient and cost-effective machine design. A practical method for engineers is the modeling of the melting process using mathematical–physical models that can be solved without complex numerical methods. These models enable rapid calculations while still providing sufficient predictive accuracy. This study revisits the modified Tadmor model by Potente, which describes the melting process and predicts the delay-zone length, extending from the hopper front edge to the point of melt pool formation. Based on extensive experimental investigations, this model is adapted by redefining the flow temperatures at the phase boundary and accounting for surface porosity at the beginning of the melting zone. Additionally, the effect of variable solid bed dynamics on model accuracy is examined. Significant model improvements were achieved by accounting for reduced heat flow into the solid bed due to the porous surface structure in the solid conveying zone, along with a new assumption for the flow temperature at the phase boundary between the solid bed and melt film. [ABSTRACT FROM AUTHOR]

Catalyst‐free, radical‐based reactive processing is used to transform low‐density polyethylene (LDPE) into polyethylene covalent adaptable networks (PE CANs) using a dialkylamino disulfide crosslinker, BiTEMPS methacrylate (BTMA). Two versions of BTMA are used, BTMA‐S2, with nearly exclusively disulfide bridges, and BTMA‐Sn, with a mixture of oligosulfide bridges, to produce S2 PE CAN and Sn PE CAN, respectively. The two PE CANs exhibit identical crosslink densities, but the S2 PE CAN manifests faster stress relaxation, with average relaxation times ∼4.5 times shorter than those of Sn PE CAN over a 130 to 160 °C temperature range. The more rapid dynamics of the S2 PE CAN translate into a shorter compression‐molding reprocessing time at 160 °C of only 5 min (vs 30 min for the Sn PE CAN) to achieve full recovery of crosslink density. Both PE CANs are melt‐extrudable and exhibit full recovery within experimental uncertainty of crosslink density after extrusion. Both PE CANs are self‐healable, with a crack fully repaired and the original tensile properties restored after 30 min for the S2 PE CAN or 60 min for the Sn PE CAN at a temperature slightly above the LDPE melting point and without the assistance of external forces. [ABSTRACT FROM AUTHOR]

Mg-based amorphous alloys have broad applications due to disordered atomic structure, thermal stability, crystallinity, low elastic modulus and high strength. In the present study, Mg–Ni–Gd–Yb–Ag alloys were prepared by vacuum arc melting combined with copper roll melt spinning. The addition of trace amounts of ytterbium (Yb) improved the corrosion resistance of Mg73-XNi15Gd10YbXAg2 (x = 2,4,6,8 at.%). Electrochemical experiments, immersion tests and analysis of corrosion products by XPS and EDS showed that Mg67Ni15Gd10Yb6Ag2 exhibited the best corrosion resistance with an Ecorr of − 968 mV and an Icorr of 5.93 µA/cm2. The superior corrosion performance was attributed to the presence of corrosion passivation films comprising MgO, Mg(OH)2, Ni(OH)2, Ag2O, AgCl, Ca5(PO4)3(OH), as well as rare-earth oxides Gd2O3 and Yb2O3. These compounds efficiently shield the matrix, and the microstructure corrosion mechanism of Mg–Ni–Gd–Yb–Ag involves a cyclic process that includes surface film layer dissolution, matrix corrosion and film layer regeneration, leading to oxide attachment. The addition of the appropriate amount of rare-earth element Yb to Mg-based amorphous alloys can improve the corrosion resistance, thereby increasing the application prospects of alloys. [ABSTRACT FROM AUTHOR]

This study explores the enhancement of poly(lactic acid) (PLA) matrix using calcium hydroxyapatite (cHAP) and reduced graphene oxide (rGO) for developing composite scaffolds aimed at bone regeneration applications. The PLA composites were fabricated through solvent evaporation and melt extrusion and characterized by various techniques, including thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and mechanical testing. The incorporation of cHAP and rGO significantly improved the thermal, mechanical, and morphological properties of the PLA matrix. Mechanical testing revealed that adding 10% cHAP and varying amounts of rGO (0.1%, 0.3%, 0.5%) enhanced tensile and compressive strengths, with the highest improvements observed at 0.5% rGO content. Thermal analysis showed increased thermal stability with higher degradation temperatures for the composites. Spectroscopic analyses confirmed the effective integration of cHAP and rGO into the PLA matrix with characteristic peaks of the fillers identified in the composite spectra. In vitro, degraded action tests in phosphate-buffered saline (PBS) at pH 7.4 over 12 months indicated that composites with higher rGO content exhibited lower mass loss and better mechanical stability. Furthermore, finite element analysis (FEA) simulations were performed to validate the experimental results, demonstrating a strong correlation between simulated and experimental compressive strengths. This novel approach demonstrates the potential of PLA/cHAP/rGO composites in creating effective and biocompatible scaffolds for tissue engineering, providing a comprehensive analysis of the synergistic effects of cHAP and rGO on the PLA matrix and offering a promising material for bone regeneration applications. [ABSTRACT FROM AUTHOR]

Biobased polymers such as polylactic acid (PLA) and polybutylene succinate (PBS) break down naturally under certain environmental conditions. The efficiency of degradation can be linked directly to fiber surface properties, which influence polymer accessibility. Here, the degradation of PLA and PBS fibers with six different cross-sections was investigated. The fibers were aged by hydrolysis and UV exposure in an accelerated weathering test, followed by an ISO 20200 laboratory-scale disintegration test with non-aged fibers as controls. The polymers were analyzed by differential scanning calorimetry, Fourier transform infrared spectroscopy, and gel permeation chromatography, comparing the polymer granulate, virgin fibers, and UV-exposed fibers. It was found that the molecular mass and crystallinity of PBS changed more than PLA during spinning. Several PLA samples were completely degraded, whereas all the PBS samples remained intact. Furthermore, surface openings appeared on the PLA fibers during weathering, suggesting greater sensitivity to UV exposure and hydrolysis than PBS. A clear correlation between the fiber surface area and the degradation rate was observed for all samples, but the correlation was positive for PLA and negative for PBS. The slower degradation of PBS fibers with a larger surface area may reflect the ability of PBS to preserve itself by further crystallization during degradation processes at temperatures higher than the glass transition point. The data clearly show that the analysis of single degradation mechanisms is insufficient to predict the behavior of material under real-world conditions, where different degradation mechanisms may work in parallel or consecutively, and may show interdependencies. [ABSTRACT FROM AUTHOR]

The escalating environmental concerns associated with conventional plastic packaging have accelerated the development of sustainable alternatives, making food packaging a focus area for innovation. Bioplastics, particularly polyhydroxyalkanoates (PHAs), have emerged as potential candidates due to their biobased origin, biodegradability, and biocompatibility. PHAs stand out for their good mechanical and medium gas permeability properties, making them promising materials for food packaging applications. In parallel, zinc oxide (ZnO) nanoparticles (NPs) have gained attention for their antimicrobial properties and ability to enhance the mechanical and barrier properties of (bio)polymers. This review aims to provide a comprehensive introduction to the research on PHA/ZnO nanocomposites. It starts with the importance and current challenges of food packaging, followed by a discussion on the opportunities of bioplastics and PHAs. Next, the synthesis, properties, and application areas of ZnO NPs are discussed to introduce their potential use in (bio)plastic food packaging. Early research on PHA/ZnO nanocomposites has focused on solvent-assisted production methods, whereas novel technologies can offer additional possibilities with regard to industrial upscaling, safer or cheaper processing, or more specific incorporation of ZnO NPs in the matrix or on the surface of PHA films or fibers. Here, the use of solvent casting, melt processing, electrospinning, centrifugal fiber spinning, miniemulsion encapsulation, and ultrasonic spray coating to produce PHA/ZnO nanocomposites is explained. Finally, an overview is given of the reported effects of ZnO NP incorporation on thermal, mechanical, gas barrier, UV barrier, and antimicrobial properties in ZnO nanocomposites based on poly(3-hydroxybutyrate), poly(3-hydroxybutyrate-co-3-hydroxyvalerate), and poly(3-hydroxybutyrate-co-3-hydroxyhexanoate). We conclude that the functionality of PHA materials can be improved by optimizing the ZnO incorporation process and the complex interplay between intrinsic ZnO NP properties, dispersion quality, matrix–filler interactions, and crystallinity. Further research regarding the antimicrobial efficiency and potential migration of ZnO NPs in food (simulants) and the End-of-Life will determine the market potential of PHA/ZnO nanocomposites as active packaging material. [ABSTRACT FROM AUTHOR]

This work investigates the effect of the microstructure of the as-quenched precursors prepared at various cooling rates on the soft magnetic characteristics and its sensitivity to the annealing heat rate (HR) of the Fe83.5Si3B10P2Cu1.5 nanocrystalline alloy. The results of Mössbauer spectra indicate that the cooling rate during the melt spinning process significantly impact the microstructure of as-quenched alloy samples. The decrease in the cooling rate facilitates the formation of an amorphous/nanocrystalline precursor containing more "α-Fe-like" structure and Cu-clusters. Variations of grain size and Hc with heating rate indicate that Fe83.5Si3B10P2Cu1.5 alloy samples prepared at a low cooling rate are less sensitive to the heating rate during crystallization annealing. The Fe83.5Si3B10P2Cu1.5 nanocrystalline alloy prepared at low cooling rate can achieve excellent soft magnetic properties with low HR annealing. [ABSTRACT FROM AUTHOR]

Carbon fiber reinforced thermoplastics (CFRTPs) demonstrate promising applications in engineering sectors, and the interfacial interaction between CFs and the matrix plays a significant role in determining the properties of CFRPs. This work attempted to study the influence of sizing agent on the properties of polyphenylene sulfide/CF (PPS/CF) composites with an aim to fabricate PPS/CF composites with enhanced mechanical properties. The results showed that the use of 2 wt% boron phenolic resin as the sizing agent favored the formation of a uniform interfacial layer on the surface of CFs. Contact angle tests revealed that corresponding sized CFs exhibited the smallest contact angle and the highest surface energy among the studied systems. As a result, the sizing agents acted as a protective layer for CFs during melt processing process, which mitigated the damage to the CFs. The average length of CFs was longer after melt extrusion process which was vital for achieving high mechanical performance of PPS/CF composites. Highlights: Coating sizing agent protected CFs from being fractured during melt processing.Applying 2 wt% BPR sizing agent yielded the best interfacial performance.The tensile strength and Yong's modulus of PPS/CFB2 reached as high as 155.9 and 7618.21 MPa.The tensile fracture mode between BPR‐treated CFs and PPS was cohesive damage. [ABSTRACT FROM AUTHOR]

Highlights Additive manufacturing for polylactic acid (PLA) reinforced with cellulose nanofibrils (CNF) could unlock fabrication of specialized and user‐specific biomedical devices. However, the process of combining PLA and CNF is challenging and proves complicated with possible irreversible CNF agglomeration and organic solvents leftover, particularly when involving solvent‐casting technique. Direct melt‐blending can mitigate these issues, but there are few reports of a single‐step melting and extrusion process to produce ready‐to‐use 3D printing filaments. This study compares the distribution of CNF fillers within the PLA matrix in PLA/CNF composites made by direct melt‐blending into filaments using a benchtop filament maker, and by solvent‐casting followed by extrusion into filaments. The filaments were 3D‐printed via fused deposition modeling (FDM), followed by tensile testing, morphology, and other characterizations. Uneven filament diameters were observed for the composite filaments prepared via solvent‐casting because of severe agglomeration, resulted in poor printability and tensile properties of filaments and 3D‐printed samples. Direct melt‐blended filament diameters were consistent, resulted in only slight decrease of tensile properties compared to pure PLA, contributing to the highest maximum tensile strength of 3D‐printed sample of 51.47 ± 1.73 MPa at 5% CNF loading. Morphology revealed good integration of CNF into PLA matrix starting at 3% CNF loading. Direct melt‐blending was comparable to the conventional methods, which enables simpler PLA/CNF composite preparation especially for 3D printing. Better dispersibility achieved by direct melt‐blending than by solvent‐casting. PLA/CNF filaments produced via solvent‐casting suffered severe agglomeration. Direct melt‐blended PLA/CNF5% yielded the highest maximum tensile strength. Morphology reveals good CNF‐PLA integration starting at 3% of CNF loading. Worsened agglomeration causing increased number of voids observed at 10% CNF. [ABSTRACT FROM AUTHOR]

Today's drugs, not all usually soluble and easy to formulate drug actives, they might be potent drug molecules at their specific target, they can never become a successful therapy, or molecule, or product if they are not able to reach the target where they are active. So, what we are targeting in this for is making these molecules bioavailable. So, this is what we want to achieve and it can be done by the melt extrusion process. The key point of this review was to establish the relationship between a novel technology, solubility and the bioavailability profile through Hot Melt Extrusion (HME) in order to reshaping the Pharmacokinetic (PK) and Pharmacodynamic (PD) landscape for poorly soluble drugs. Tailoring the PK and PD with HME solid dosage form was shown to be affected by the physicochemical properties of the carrier matrix used. With the help of HME technology by dissolving these crystalline drug actives in a molten polymer matrix and pre-dissolved form and that makes it much more bioavailable and this enhanced the performance of such drug actives and in many cases. It is that what actively enables such molecules to at all become a drug product and a therapy. Compared to the traditional methods of developing drug products, HME is a key the gate to enhance in delivering the drug products to avoid patient compliance. A report says there are lots of developments in pharmaceutical APIs with poor solubility and improving their solubility is quite challenging. The effective formulation needs characteristics carriers and polymers that are suitable for the HME technology that has been discussed here. HME has been proven as an effective choice for the conventional ways of producing tablets, films, implants, etc. that can be administered orally, transdermal and transmucosal. This review paper adds knowledge of supercharging sluggish drugs by the use of HME and it can put the punch back in pharmaceutical industries and should use these recent developments to employ and develop cutting-edge drug delivery systems to avoid patient compliance. [ABSTRACT FROM AUTHOR]

Background/Objectives: This study compared two pilot scale continuous manufacturing methods of solid self-emulsifying drug delivery systems (SEDDSs) via hot melt extrusion (HME). Methods: A model poorly water-soluble drug carvedilol in low dose (0.5–1.0% w/w) was processed in HME either in a conventional powder form or pre-dissolved in the liquid SEDDS. Results: HME yielded a processable final product with up to 20% w/w SEDDS. Addition of carvedilol powder resulted in a non-homogeneous drug distribution in the extrudates, whereas a homogeneous drug distribution was observed in pre-dissolved carvedilol. SEDDSs were shown to have a plasticizing effect, reducing the HME process torque up to 50%. Compatibility between excipients and carvedilol in the studied ratios after HME was confirmed via DSC and WAXS, demonstrating their amorphous form. Solid SEDDSs with Kollidon® VA64 self-emulsified in aqueous medium within 15 min with mean droplet sizes 150–200 nm and were independent of the medium temperature, whereas reconstitution of Soluplus® took over 60 min and mean droplet size increased 2-fold from 70 nm to 150 nm after temperature increased from 25 °C to 37 °C, indicating emulsion phase inversion at cloud point. Conclusions: In conclusion, using Kollidon® VA64 and pre-dissolved carvedilol in SEDDS has shown to yield a stabile HME process with a homogenous carvedilol content in the extrudate. [ABSTRACT FROM AUTHOR]

A study was carried out to prepare a magnet with a c-axis alignment present in the melt-spun ribbons to be used as a precursor magnet for the hot deformation process. Melt-spun ribbons prepared at a wheel speed of 23 m/s resulted in nanograins with columnar grains having the <001> texture on the exposed side and very fine equiaxed nanograins on the wheel side of the ribbon. The ribbons were stacked and consolidated using the SPS technique with the variation of temperature (temperature series) and pressure (pressure series), which resulted in Nd2Fe14B grains in two-grain zones, namely (i) fine grain and (ii) coarse grain zones. The fine grains grow with temperature and dominate the coercivity mechanism in the temperature series, and the grains do not grow in the pressure series; hence, the coercivity is not affected by pressure. The calculation of the intensity ratio of I(006)/I(105) in SPS compacted samples in both temperature and pressure series showed evidence of texture retention; however, the texture was not strong enough to influence the magnetic properties. The best magnetic properties of Hc of 12.2 kOe and (BH)max of 11.6 MGOe were obtained in the temperature series sample prepared at temperature of 600 °C, pressure of 150 MPa, and dwell time of 2 min. [ABSTRACT FROM AUTHOR]

The preparation and characterization of composite materials composed of polypropylene (PP) as the base mixed with halloysite nanotubes (HNT) at various weight percentages (0.5, 1.5, and 3 wt.%) using a melt extrusion method operated at a temperature between 190 °C and 200 °C is described. The impact of the addition of the HNT filler on the PP nanocomposites was investigated based on the thermal and mechanical properties. The thermal characterization was conducted by differential scanning calorimetry (DSC). Significant increases in the rheological properties were observed with the addition of a high content of HNTs. The water absorption decreased with increasing HNT. The SEM micrographs showed that the HNT fillers were homogeneously dispersed throughout the entire PP matrix. [ABSTRACT FROM AUTHOR]

Additive manufacturing of pharmaceutical formulations offers advanced micro-structure control of oral solid dose (OSD) forms targeting not only customised dosing of an active pharmaceutical ingredient (API) but also custom-made drug release profiles. Traditionally, material extrusion 3D printing manufacturing was performed in a two-step manufacturing process via an intermediate feedstock filament. This process was often limited in the material space due to unsuitable (brittle) material properties, which required additional time to develop complex formulations to overcome. The objective of this study was to develop an additive manufacturing MicroFactory process to produce an immediate release (IR) OSD form containing 250 mg of mefenamic acid (MFA) with consistent drug release. In this study, we present a single-step additive manufacturing process employing a novel, filament-free melt extrusion 3D printer, the MicroFactory, to successfully print a previously 'non-printable' brittle Soluplus®-based formulation of MFA, resulting in targeted IR dissolution profiles. The physico-chemical properties of 3D printed MFA-Soluplus®-D-sorbitol formulation was characterised by thermal analysis, Fourier Transform Infrared spectroscopy (FTIR), and X-ray Diffraction Powder (XRPD) analysis, confirming the crystalline state of mefenamic acid as polymorphic form I. Oscillatory temperature and frequency rheology sweeps were related to the processability of the formulation in the MicroFactory. 3D printed, micro-structure controlled, OSDs showed good uniformity of mass and content and exhibited an IR profile with good consistency. Fitting a mathematical model to the dissolution data correlated rate parameters and release exponents with tablet porosity. This study illustrates how additive manufacturing via melt extrusion using this MicroFactory not only streamlines the manufacturing process (one-step vs. two-step) but also enables the processing of (brittle) pharmaceutical immediate-release polymers/polymer formulations, improving and facilitating targeted in vitro drug dissolution profiles. [ABSTRACT FROM AUTHOR]

Black ginseng (BG), a traditional medicinal herb produced through a nine-stage steaming and drying process, exhibits stronger pharmacological efficacy, including antioxidant, anti-inflammatory, and anti-cancer properties, when compared to white and red ginseng. The ginsenosides in BG are classified as major and minor types, with minor ginsenosides demonstrating superior pharmacological properties. However, their low concentrations limit their availability for research and clinical applications. In this study, hot melt extrusion (HME) was utilized as an additional processing technique to enhance the content of minor ginsenoside in BG, and the physicochemical properties of the formulation were analyzed. Ginsenoside content in BG and HME-treated BG (HME-BG) was analyzed using high-performance liquid chromatography (HPLC), while their physicochemical properties were evaluated through dynamic light scattering (DLS), electrophoretic light scattering (ELS), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and Fourier-transform infrared spectroscopy (FT-IR). HME treatment resulted in a significant increase in minor ginsenosides Rg3 and compound K (CK) by 330% and 450%, respectively, while major ginsenosides Rg1 and Rb1 decreased or were not detected. Additionally, HME-BG demonstrated reduced particle size, improved PDI, and decreased crystallinity. HME treatment effectively converts major ginsenosides in BG into minor ginsenosides, enhancing its pharmacological efficacy and showing great potential for research and development applications. [ABSTRACT FROM AUTHOR]

As a promising innovative energy storage material, phase change fibers (PCFs) have been widely studied. PCFs are equipped with the ability of temperature regulation by introducing phase change materials (PCMs) and have been successfully prepared by melt spinning, wet spinning and electrospinning. With the rapid development of PCM and fibrous preparation technology, the combination of different processes of PCF preparation has been explored and developed. In this paper, the research progress of the preparation methods of PCFs is reviewed. Firstly, the preparation methods are classified according to the different loading forms of PCMs, and the fibrous maceration method, composite method and microcapsule method are introduced. Then, the special preparation methods and characteristics of PCF are elaborated. Finally, the research hot spots and development of PCFs are summarized for providing guidance for fabricating PCFs with desired comprehensive properties; among them, with the continuous innovation of smart fibers, the single function of PCFs will cause limited use, so the multi-functionality of PCFs is also discussed in detail for various applications. [ABSTRACT FROM AUTHOR]

Ti-V-based alloys are proved of huge potential in storing hydrogen, but the incomplete reversible hydrogen storage capacity caused by overstability of V hydride has limited the large-scale application. In this study, Ti32V40+xFe23-xMn5 (x=0, 4, 8, 12, at.%) alloys were designed, and the effects of V/Fe ratio on phase constitution and hydrogen storage properties were investigated. The main phase of the alloys is body-centered cubic (BCC) phase, and the lattice constants of the BCC phase decrease with the decrease of V/Fe ratio. Moreover, C14 Laves phase exists in alloys with a Fe content of 19at.% to 23at.%. For hydrogenation, the C14 Laves phase can accelerate the hydrogen absorption rate, but the hydrogen absorption capacity is reduced. With the decrease of V/Fe ratio, the hydride gradually destabilizes. Owing to its large lattice constant and high hydrogen absorption phase content, the Ti32V52Fe11Mn5 alloy shows the most enhanced hydrogen storage properties with hydrogenation and dehydrogenation capacities of 3.588wt.% at 298 K and 1.688wt.% at 343 K, respectively. The hydrogen absorption capacity of this alloy can be reserved to 3.574wt.% after 20 cycles of hydrogen absorption and desorption. [ABSTRACT FROM AUTHOR]

Polyamide composites with varying filler concentrations are prepared using the hot melt extrusion method, employing polyamide 56/6 (PA56/6) and modified talc as fillers. Initially, the thermal characteristics of PA56/6 composites (PA56/6‐talc) are examined through thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC), encompassing parameters such as melting temperature, crystallinity, and decomposition temperature. The hydrophilicity and barrier properties of PA56/6‐talc are assessed using an optical contact angle meter, a water vapor transmission rate tester, and an oxygen transmission rate tester. Furthermore, the mechanical properties of PA56/6‐talc are also scrutinized. The results indicate that PA56/6 exhibits superior hydrophobic, barrier, and mechanical properties, thereby demonstrating its immense potential in garment fabrics and packaging materials. [ABSTRACT FROM AUTHOR]

This study examines the impact of Pineapple Leaf Fiber (PALF) loading on the properties of High-Density Polyethylene (HDPE)/PALF composites successfully produced through a melt extrusion process. The melt-extruded HDPE/PALF composites were characterized by their thermal and mechanical properties and their morphologies. Subsequently, adding 5% maleic anhydride (MA) to the HDPE/PALF composite formulation led to significant improvements in the mechanical strength properties. Moreover, adding 10 wt.% PALF and 5% MA to the composites improves the crystallinity (10.38%) and Young's modulus (17.30%) properties and affects the thermal stability. The optimal formulation is achieved with 10 wt.% PALF filler incorporated into the HDPE composite. This study highlights the promising potential of HDPE/PALF composites for plastic product applications. [ABSTRACT FROM AUTHOR]

Polymer fibers are considered ideal transmission media for all-optical networks, but their high intrinsic loss significantly limits their practical use. Quantum dot-doped polymer fiber amplifiers are emerging as a promising solution to this issue and are becoming a significant focus of research in both academia and industry. Based on the properties of CdSe/ZnS quantum dots and PMMA material, this study experimentally explores three fabrication methods for CdSe/ZnS quantum dots-doped PMMA fibers: hollow fiber filling, melt-drawing, and melt extrusion. The advantages and disadvantages of each method and key issues in fiber fabrication are analyzed. Utilizing the CdSe/ZnS quantum dots-doped PMMA fibers that were fabricated, we theoretically analyzed the key factors affecting gain performance, including fiber length, quantum dots doping concentration, and signal light intensity. Under the conditions of 1.5 W power and 445 nm laser pumping, a maximum on-off gain of 16.2 dB was experimentally achieved at 635 nm. Additionally, using a white light LED as the signal source, a broadband on-off gain with a bandwidth exceeding 70 nm and a maximum gain of 12.4 dB was observed in the 580–650 nm range. This research will contribute to the development of quantum dots-doped fiber devices and broadband optical communication technology, providing more efficient solutions for future optical communication networks. [ABSTRACT FROM AUTHOR]

In response to an investigation on the paths of changes in the crystallization and radial differences during the forming process of nascent fibers, in this study, we conducted numerical simulation and analyzed the changes in crystallization mechanical parameters and tensile properties through a fluid dynamics two-phase model. The model was based on the melt-spinning method focusing on melt spinning, the environment of POLYFLOW, and the method of joint simulation, coupled with Nakamura crystallization kinetics, including the development of process collaborative parameters, stretch-induced crystallization, viscoelasticity, filament cooling, gravity term, inertia, and air resistance. Finally, for nylon 6 BHS and CN9987 resin spinning, the model successfully predicted the distribution changes in temperature, velocity, strain rate tensor, birefringence, and stress tensor along the axial and radial fibers and obtained the variation pattern of fibers' crystallinity along the entire spinning process under different stretching rates. Furthermore, we also explored the effects of spinning conditions, including inlet flow rate, winding speeds, and the extrusion temperature, on the fibers' crystallization process and obtained the influence rules of different spinning conditions on fiber crystallization. Knowing the paths of changes in mechanical performance can provide important guidance and optimization strategies for the future industrial preparation of high-performance fibers. [ABSTRACT FROM AUTHOR]

Plastic recycling, waste minimization such as process outfall valorization promotes a circular economy. Herein, food trays have been produced in the moulded pulp thermoforming process. To this end, high-density polyethylene (HDPE) outfall has been dispersed in water via Poly vinyl alcohol (PVA) addition in a Northern Bleached Softwood Kraft Pulp (NBSKP) slurry. Samples physical and mechanical properties have been evaluated. With an increasing HDPE content, parts air permeability was drastically reduced to a minimum of 2.4 ± 0.8 mL min−1. In addition, water and grease hold out properties have been increased with minimum water Cobb1800 value of 10.9 ± 5.4 gm−2 and oil Cobb1800 value of 13.18 ± 6.5 gm−2. Samples with high HDPE content demonstrated hydrophobic surface with water contact angle value above 90°. HDPE melting and binding to wood pulp fibers was monitored by SEM images. Regarding the mechanical properties, HDPE induced plastic deformation with a reduced Young modulus by 17 %. Moreover, the addition of HDPE increased wet strength by 81 %. However, the produced food tray composites with high HDPE content demonstrated low repulpability index. [ABSTRACT FROM AUTHOR]

In this paper, linear low-density polyethylene (LLDPE) fibers were stabilized by ultraviolet ray (UV) irradiation, which provided a new treatment method for fabricating carbon fiber precursors. LLDPE chips were blended with a photo-initiator 4-chlorobenzophenone (4-CBP) and a crosslinker 1,2-polybutadiene (1,2-PB) to obtain spun particles, and then they were melt spun into the fibers. Then, UV irradiation of the as-spun fibers was performed to obtain precursors. An orthogonal experimental design investigated the effects of the ingredient ratio LLDPE:1,2-PB and UV irradiation time on the fiber gelation. The results show that the factor's order of influence was: ingredient ratio > UV irradiation time. The fiber gelation reaches a maximum of 67.51% at a dosage ratio of LLDPE:1, 2-PB of 97:2, and a UV irradiation time of 30 min. The UV irradiation introduced the crosslinking structure of LLDPE fibers, and the melting temperature of UV-XLPE fibers shifts toward lower temperatures, and the crystal size of the fibers decreased with increasing UV irradiation time. However, longer irradiation time does not beneficially affect the gelation degree. The low cost and feasible crosslinking method in this study offer the possibility of wide application of low-cost polyethylene-based carbon fibers. [ABSTRACT FROM AUTHOR]

Fiber-based technologies are widely used in various industries, but their use in pharmaceuticals remains limited. While melt extrusion is a standard method for producing medical fibers such as sutures, it is rarely used for pharmaceutical fiber-based dosage forms. The EsoCap system is a notable exception, using a melt-extruded water-soluble filament as the drug release trigger mechanism. The challenge of producing drug-loaded fibers, particularly due to the use of spinning oils, and the processing of the fibers are addressed in this work using other approaches. The aim of this study was to develop processes for the production and processing of pharmaceutical fibers for targeted drug delivery. Fibers loaded with polyvinyl alcohol and fluorescein sodium as a model drug were successfully prepared by a continuous melt extrusion process and directly spun. These fibers exhibited uniform surface smoothness and consistent tensile strength. In addition, the fibers were further processed into tubular dosage forms using a modified knitting machine and demonstrated rapid drug release in a flow cell. [ABSTRACT FROM AUTHOR]

The present study investigated the effect of different polymers and manufacturing methods (hot melt extrusion, HME, and spray drying, SD) on the solid state, stability and pharmaceutical performance of amorphous solid dispersions. In the present manuscript, a combination of different binary amorphous solid dispersions containing 20% and 30% of drug loadings were prepared using SD and HME. The developed solid-state properties of the dispersions were evaluated using small- and wide-angle X-ray scattering (WAXS) and modulated differential scanning calorimetry (mDSC). The molecular interaction between the active pharmaceutical ingredients (APIs) and polymers were investigated via infrared (IR) and Raman spectroscopy. The in vitro release profile of the solid dispersions was also evaluated to compare the rate and extend of drug dissolution as a function of method of preparation. Thereafter, the effect of accelerated stability conditions on the physicochemical properties of the solid dispersions were also evaluated. The results demonstrated higher stability of Soluplus® (SOL) polymer-based solid dispersions as compared to hydroxypropyl methylcellulose (HPMC)-based solid dispersions. Moreover, the stability of the solid dispersions was found to be higher in the case of API having high glass transition temperature (Tg) and demonstrated higher interaction with the polymeric groups. Interestingly, the stability of the melt-extruded dispersions was found to be slightly higher as compared to the SD formulations. However, the down-processing of melt-extruded strands plays critical role in inducing the API crystal nuclei formation. In summary, the findings strongly indicate that the particulate properties significantly influence the performance of the product. [ABSTRACT FROM AUTHOR]

Curcumin and piperine are plant compounds known for their health-promoting properties, but their use in the prevention or treatment of various diseases is limited by their poor solubility. To overcome this drawback, the curcumin–piperine amorphous polymer–phospholipid dispersions were prepared by hot melt extrusion technology. X-ray powder diffraction indicated the formation of amorphous systems. Differential scanning calorimetry confirmed amorphization and provided information on the good miscibility of the active compound–polymer–phospholipid dispersions. Owing to Fourier-transform infrared spectroscopy, the intermolecular interactions in systems were investigated. In the biopharmaceutical properties assessment, the improvement in solubility as well as the maintenance of the supersaturation state were confirmed. Moreover, PAMPA models simulating the gastrointestinal tract and blood-brain barrier showed enhanced permeability of active compounds presented in dispersions compared to the crystalline form of individual compounds. The presented paper suggests that polymer–phospholipid dispersions advantageously impact the bioaccessibility of poorly soluble active compounds. [ABSTRACT FROM AUTHOR]

There is a growing need to address waste generated from Fused Filament Fabrication (FFF) 3D printing activities. This study explores the mechanical recycling of waste polylactic acid (PLA) accumulated from failed 3D printing operations and PLA biocomposite filaments containing nanocellulose fibres. FFF 3D printable filaments were produced via melt mixing and extrusion of virgin PLA containing varying amounts of waste PLA. The chemical, thermal and thermomechanical characterisation of each specimen was evaluated using Fourier‐transform infrared spectroscopy (FTIR), simultaneous thermal analysis (SDT), dynamic mechanical analysis (DMA), and uniaxial tensile analysis (UTA). A desktop FFF 3D printer was used to fabricate UTA and DMA test specimens. The thermal stability of the filament specimens containing waste derived from the failed 3D prints were comparable with that of the commercial filaments. However, a 11% decrease in the onset of thermal degradation is observed for the filament containing waste biocomposites. The specimens containing waste PLA exhibited higher crystallinity and storage modulus. UTA results revealed similar tensile strength and % elongation, except for the specimen containing 50% waste PLA which exhibited a 29% decrease in tensile strength. This work successfully demonstrates mechanical recycling as a viable waste management strategy for waste materials generated during FFF 3D printing. [ABSTRACT FROM AUTHOR]

Magnetic phase transition and magnetocaloric effect in the amorphous Gd52Fe28B20 alloy are exhaustively explored. The melt spinning technique was employed to produce the amorphous alloy. Considering the Landau theory and Banerjee criterion, the nature of the magnetic phase transition (MPT) follows a second order MPT at the Curie temperature (TC) from ferromagnetic to paramagnetic states. The Maxwell thermodynamic relation was used to calculate the maximum isothermal entropy change (− ∆SM). This alloy exhibits wide peaks in entropy versus temperature curves, which is advantageous for enhancing the relative cooling power (RCP). The RCP of Gd52Fe28B20 was found to be ~ 190 J kg−1 (at TC = 260 K, µ0H = 2 T), the value similar to that obtained in pure Gd (at TC = 293 K, µ0H = 2 T). Additionally, we provide a phenomenological model related to the theoretical assessment of the magnetocaloric effect. The dependence of theoretical parameters on temperature and magnetic field was established through rigorous analysis. The accuracy of these theoretical predictions was assessed by comparing them to experimental results. Consequently, this alloy is appropriate for use near the ordering temperature of 260 K, which bodes well for the development of novel magnetic refrigerants for active cooling applications. [ABSTRACT FROM AUTHOR]

The facile characterization of isothermal microphase separation kinetics in polyamide 6 (PA6)‐based thermoplastic elastomers (TPAE‐6) has long posed a challenge for the development of suitable melt spinning processes. In this study, this challenge is addressed through differential scanning calorimetry (DSC) measurements. It is assumed that the enthalpy changes of TPAE‐6 during the isothermal process are a linear superposition of enthalpy changes associated with microphase separation and crystallization of PA6 in hard phases, resembling that of TPAE‐6 without soft segments (TPAE‐6‐0). The study reveals that, as the concentration of soft segments in TPAE‐6 increases, the accelerated dynamics of phase separation become stronger than the dilution of soft segments to PA6 segments during isothermal process, resulting in an increase in the microphase separation rate of TPAE‐6. Furthermore, despite microphase separation, the overall crystallization rate of TPAE‐6 decreases with rising isothermal temperature and varies with increasing soft segment content at different temperatures. Additionally, the crystallization mode of TPAE‐6 follows two‐dimensional, three‐dimensional, or a combination of both crystal growth mechanisms, accompanied by a heterogeneous nucleation mechanism. [ABSTRACT FROM AUTHOR]

The document titled "Bayesian chronological analyses consistent with synchronous age of 12,835-12,735 Cal B.P. for Younger Dryas Boundary on four continents" discusses the limitations and challenges of radiocarbon and optically stimulated luminescence (OSL) dating methods. It emphasizes the importance of integrating dating methods with other stratigraphic information and using Bayesian analysis to improve accuracy. The document provides information on various sites that have been studied in relation to the Younger Dryas Boundary (YDB) event, including their location, proxies found, and age estimates. It also discusses the evidence of impact-related proxies found at these sites, supporting the hypothesis of a cosmic impact event around 12,800 years ago. The document includes age models, chronological information, and statistical data for specific sites, as well as references to related research. [Extracted from the article]

We applied computing-as-a-service to the unattended system-agnostic miscibility prediction of the pharmaceutical surfactants, Vitamin E TPGS and Tween 80, with Copovidone VA64 polymer at temperature relevant for the pharmaceutical hot melt extrusion process. The computations were performed in lieu of running exhaustive hot melt extrusion experiments to identify surfactant-polymer miscibility limits. The computing scheme involved a massively parallelized architecture for molecular dynamics and free energy perturbation from which binodal, spinodal, and mechanical mixture critical points were detected on molar Gibbs free energy profiles at 180 °C. We established tight agreement between the computed stability (miscibility) limits of 9.0 and 10.0 wt% vs. the experimental 7 and 9 wt% for the Vitamin E TPGS and Tween 80 systems, respectively, and identified different destabilizing mechanisms applicable to each system. This paradigm supports that computational stability prediction may serve as a physically meaningful, resource-efficient, and operationally sensible digital twin to experimental screening tests of pharmaceutical systems. This approach is also relevant to amorphous solid dispersion drug delivery systems, as it can identify critical stability points of active pharmaceutical ingredient/excipient mixtures. [ABSTRACT FROM AUTHOR]

Parallel micropillars of quasicrystal approximants are fabricated in Al20Si20Mn20Fe20Ga20 high-entropy alloy via melt spinning, and their micromorphology is observed by scanning electron microscopy. Unlike the traditional quasicrystal system where the crystal structure of the decagonal prism is decagonal quasicrystal, the crystal structure of micropillars reported here is identified as the orthorhombic (1/0, 2/1) quasicrystal approximant (a = 0.73 nm, b = 1.23 nm, c = 2.24 nm) through transmission electron microscopy. The cross-section structure of the micropillars consists of multiple twinned (1/0, 2/1) approximant domains or alternating splicing of (1/0, 2/1) and defective (1/0, 2/1) quasicrystal approximants. The thermal stability and the microstructure evolutions of micropillars after being heat treated are also investigated. Meanwhile, the nanomechanical properties of micropillars are characterized. [ABSTRACT FROM AUTHOR]

Polyamide-6 (PA6), or nylon-6, is a widely used low-cost polymer material for various applications. Manufacturing PA6 into fibers involves a spinning process which orients the polymer chains into a semicrystalline structure. The most economical spinning process for PA6 fibers is melt extrusion. When stretching the produced fibers to high strains, the PA6 fibers transition the metastable γ phase back into the stable α phase. The effects of these large stretches on mechanical properties have not been explored after the stretch has been released. In this study, the effects on mechanical properties were studied by stretching the PA6 fibers from 10 to 50% tensile strain and subsequently releasing the fibers. The stretched fibers were characterized by X-ray diffraction and atomic force microscopy to determine the changes to the crystal structure and surface roughness. The stretched fibers were then tensile tested to failure and the tensile properties were examined. The stress-strain curves on the post-stretched PA6 fibers showed clear softening in the fibers with lower initial moduli after 30% stretching. These results may hold a clue to softening of fibers in applications with repeated loading and have implications for mechanical stability and fatigue of this polymeric material. [ABSTRACT FROM AUTHOR]

Impact of shot peening on SS347 tube has been investigated using MagStrics, a magnetostrictive sensing (MsS) device comprising of rapidly quenched ribbon as sensor element. Two tubes of SS347 have been considered in pre- and post-shot peened state. Annealed ribbon as sensor element showed enhanced MsS signal. Using the annealed ribbon as sensor element, the MsS signal amplitude in shot peened tube was found to be distinctly different from un-peened sample. This was associated to magnetic phase evolutions in the pipe internal surface due to shot peening. Such phenomena have been endorsed through SEM–EDX compositional analysis and correlated through simulations using COMSOL Multiphysics. [ABSTRACT FROM AUTHOR]

Excellent soft magnetic properties of the amorphous and nanocrystalline alloys are attributed to their unique microstructure. In this work, Fe73.5Si13.5-xNb3Cu1B9Px (x = 0, 3.5, 7, 10 at. %) amorphous ribbons have been fabricated using the melt spinning technique. The effect of annealing temperature (475 ~ 600 ℃) on the microstructure and soft magnetic properties have been studied. According to the results, the thermal stability of FeSiNbCuBP amorphous alloys was improved by the partial substitution of Si by P. Moreover, it was found that the grain growth of α-Fe (Si) phase can be restrained by the appropriate amount of P addition and result to a grain refinement of the alloys during annealing. Base on refinement grain size (9 nm) and optimal crystallization volume fraction (47%), Fe73.5Si10Nb3Cu1B9P3.5 nanocrystalline alloy with low coercivity of 0.02 A/m and high effective permeability of 3.22 × 104 was developed after annealed at 525 ℃. Besides, we propose that the migration of free electrons from P to Fe could diminish the saturation magnetization of these alloys. [ABSTRACT FROM AUTHOR]

Various experimental methods are used to examine the effect of cooling rate on the magnetic properties of magnetic materials, such as melt spinning at different wheel speeds. To shed light on these experimental studies as a theoretical study, we used a mixed spin (1, 3/2) Ising system on a square lattice under an oscillating magnetic field within the path probability method. It is very advantageous to use the path probability method in such studies, because it explains the dynamic magnetic phase behaviors and dynamic hysteresis curves of the system depending on all system parameters, and one of the coupling parameters ( k 2 ) arising in this method corresponds to the wheel speed (rate constant) in the melt spinning method. In this study, dynamic hysteresis curves of a magnetic material were obtained for different k 2 parameters as well as other system parameters, namely reduced temperature, crystal field interaction, and angular frequency. In some magnetic materials, hard and soft magnetic hysteresis loop behaviors and single and multiple hysteresis loop behaviors have been obtained, which have been reported theoretically as well as experimentally. The results shed light on experimental workers who were unable to reach higher wheel speeds using the melt-spinning method. [ABSTRACT FROM AUTHOR]

Casting speed, casting temperature and secondary cooling water flow rate are the main process parameters affecting the DC casting process. These parameters significantly influence the flow and temperature fields during casting, which are crucial for the quality of the ingot and can determine the success or failure of the casting operation. Numerical simulation, with the advantages of low cost, rapid execution, and visualized results, is an important method to study and optimize the DC casting process. In the present work, a simulation model of DC casting 2024 aluminum alloy was established, and the reliability of the model was verified. Then, the influence of casting parameters on flow field and temperature field was studied in detail by numerical simulation method. Results show that with the increase of casting speed, the melt flow becomes faster, the depths of slurry zone and mushy zone increase, and the variation of slurry zone depth is greater than that of mushy zone. With an increase in casting temperature, the melt flow rate increases, the depth of the slurry zone becomes shallower, and the depth of the mushy zone experiences only minor changes. The simulation results further indicate that the increase of the flow rate of the secondary cooling water slightly reduces the depths of both slurry and mushy zone. [ABSTRACT FROM AUTHOR]

Bi1−xSbx alloys with large linear magnetoresistance (LMR) are a promising candidate for magneto-electronic devices. In this work, the highly (00l) textured Bi1−xSbx (0 ≤ x ≤ 0.04) ribbons with nano-sized lamellar grains were prepared by the melt spinning method and their magneto-transport properties were investigated. All the ribbons exhibit obvious LMR features, and the crossover magnetic field (Bc) from quadratic to linear magnetoresistance is remarkably reduced by Sb doping. Compared with the Bc of the x = 0 ribbon (about 1.28 T at 300 K), the Bc values of the Sb doped ribbons are significantly smaller, especially for the Bc of the x = 0.03 ribbon (only about 0.53 T at 300 K). Besides, for the x = 0.03 ribbon, the parameter Φ (MR%(B = 1 T)/Bc) relevant to LMR performance reaches up to 52 at 300 K. Analysis of the LMR reveals that Sb doping makes the LMR mechanism transition from recombination of carriers for x = 0 ribbon to spatial fluctuation of carrier mobility governed LMR for x = 0.03 ribbon. This work is instructive to understand the transport features of textured Bi1−xSbx ribbons. [ABSTRACT FROM AUTHOR]

The fabrication of a biodegradable polycaprolactone (PCL)/hydroxyapatite (HAp) scaffold prepared from local waste blue crab shells (Portunus pelagicus) by melt spinning method was investigated. The effect of different KH2PO4 concentrations on the physico‐chemical properties of HAp is evaluated. Furthermore, the influence of PCL/HAp ratios on mechanical strength and particle size distribution is reported. The formation of HAp is confirmed by Infrared (IR) spectroscopy and X‐ray diffraction (XRD). The biocompatibility of the PCL/HAp composites was evaluated using MTT assay and mechanical tests. The results reveal that the increase in KH2PO4 concentration contributed to the higher yield of HAp. However, the crystal and particle sizes are relatively invariable. SEM micrograph shows that the HAp introduction into PCL improves the material's porosity. Moreover, adding 10 % HAp into the PCL matrix significantly improved the mechanical strength of the filament compared to commercial PCL. MTT assay exhibits above 90 % cell viability, implying that the prepared PCL/HAp composite is non‐toxic and biocompatible with artificial bone replacement. After all, this study demonstrates that PCL/HAp filament derived from local blue crab waste is highly promising as a bone scaffolding material. [ABSTRACT FROM AUTHOR]

Metallic alloys often form phases--known as solid solutions--in which chemical elements are spread out on the same crystal lattice in an almost random manner. The tendency of certain chemical motifs to be more common than others is known as chemical short-range order (SRO), and it has received substantial consideration in alloys with multiple chemical elements present in large concentrations due to their extreme configurational complexity (e.g., high-entropy alloys). SRO renders solid solutions "slightly less random than completely random," which is a physically intuitive picture, but not easily quantifiable due to the sheer number of possible chemical motifs and their subtle spatial distribution on the lattice. Here, we present a multiscale method to predict and quantify the SRO state of an alloy with atomic resolution, incorporating machine learning techniques to bridge the gap between electronic-structure calculations and the characteristic length scale of SRO. The result is an approach capable of predicting SRO length scale in agreement with experimental measurements while comprehensively correlating SRO with fundamental quantities such as local lattice distortions. This work advances the quantitative understanding of solid-solution phases, paving the way for the rigorous incorporation of SRO length scales into predictive mechanical and thermodynamic models. [ABSTRACT FROM AUTHOR]