Commercial Powder Research Articles

Ready-to-use ratiometric bioluminescence immunosensor for detection of ochratoxin a in pepper

Rapid, portable, and accurate detection tools for monitoring ochratoxin A (OTA) in food are essential for the guarantee of food safety and human health. Herein, as a proof-of-concept, this study proposed a ratiometric bioluminescence immunosensor (RBL-immunosensor) for homogeneous detection of OTA in pepper. The construct of the RBL-immunosensor consists of three components, including the large fragment of the split nanoluciferase (NanoLuc)-tagged nanobody (NLg), the small fragment of the split NanoLuc-tagged mimotope peptide heptamer (MPSm), and the calibrator luciferase (GeNL). The specific nanobody-mimotope peptide interaction between NLg and MPSm induces the reconstitution of the NanoLuc, which catalyzes the Nano-Glo substrate and produces a blue emission peak at 458 nm. Meanwhile, GeNL can produce a green emission peak at 518 nm upon substrate conversion via bioluminescent resonance energy transfer (BRET). Therefore, the concentration of OTA can be linked to the variation of the bioluminescence signal (λ458/λ518) measured by microplate reader and the variation of the blue/green ratio measured by smartphone via the competitive immunoreaction where OTA competes with MPSm to bind NLg. The immunosensor is ready-to-use and works by simply mixing the components in a one-step incubation of 10 min for readout. It has a limit of detection (LOD) of 0.98 ng/mL by a microplate reader and an LOD of 1.89 ng/mL by a smartphone. Good selectivity and accuracy were confirmed for the immunosensor by cross-reaction analysis and recovery experiments. The contents of OTA in 10 commercial pepper powder samples were tested by the RBL-immunosensor and validated by high-performance liquid chromatography. Hence, the ready-to-use RBL-immunosensor was demonstrated as a highly reliable tool for detection of OTA in food.

Utilization of Slip Casting Process for Recycling CAD/CAM Dental Zirconia Wastes

This study aimed to find the ideal parameters for shaping waste zirconia powders from dental laboratories using the slip-casting process. Additionally, the qualities of ceramic products created in this manner were evaluated using microstructural characterization and physical-mechanical tests. Various dental laboratories provided the waste CAD/CAM zirconia powder used in the investigation. Wastes in powder form were first calcined. Afterward, an attritor mill was used to grind the grain size until it was usable, following the completion of the grain size distribution analysis. Waste and commercial zirconia powders were combined using various dispersants to create slip-casting slurries. The rheological characteristics of these slurries were then ascertained. By evaluating the rheological properties of slip-casting slurries prepared in this way, the most suitable casting parameters were determined, and ceramic products were formed by slip-casting technique from the slurries to be prepared in accordance with these parameters. The shaped samples were dried and sintered at two different temperatures, 1400-1450°C, and samples were designed for physical, mechanical, and microstructural characterization. The pore percentages, bulk densities, and water absorption of the sintered samples, according to Archimedes’ principle, as well as their strengths, were determined by the three-point bending strength test. Phase analysis was performed with XRD (X-ray diffractometer) microstructure studies with SEM (Scanning Electron Microscopy). It has been concluded that waste zirconia can be used in dental applications.

Microstructural Characterization of AlCrCuFeMnNi Complex Concentrated Alloy Prepared by Pressureless Sintering.

A significant and increasing number of studies have been dedicated to complex concentrated alloys (CCAs) due to the improved properties that these metallic materials can exhibit. However, while most of these studies employ melting techniques, only a few explore powder metallurgy and pressureless sintering as production methods. In this work, a microstructural characterization of AlCrCuFeMnNi CCA samples obtained by powder metallurgy and pressureless sintering using mixtures of powders with different compositions was carried out. One batch of samples (B1) was prepared using commercial powders of Al, Cr, Cu, Fe, Mn, and Ni. Another batch (B2) used mixtures of CrFeMn, AlNi, and Cu powders. A third set of samples (B3) was obtained by adding 1% at. of Mg to the B2 powder. The samples were characterized by X-ray diffraction, scanning and transmission electron microscopy, energy dispersive spectroscopy, density measurements, and hardness tests. Thermodynamic calculations were also used to complement the microstructural characterization. All the obtained samples exhibited high relative density and hardness values. However, B3 samples showed a higher hardness, attributed to the finer distribution of oxide particles, which was promoted by the presence of Mg during sintering. These last samples presented a hardness/density ratio of 62 HV/(g cm-3), surpassing that of some martensitic stainless steels and nickel-titanium alloys.

Characterization and application of synthesized calcium alginate-graphene oxide for the removal of Cr3+, Cu2+ and Cd2+ ions from tannery effluents

Environmental sustainability has gained acceptance to achieving the goal of a secure ecosystem with a reliable management system. Heavy metal remediation of aqueous streams is of special concern due to the intractability and persistence in the environment. Adsorption is a potential alternative to the existing inefficient conventional technologies for the removal and recovery of metal ions from aqueous solutions and becomes vital to align with the Sustainable Development Goals (SDGs) and mitigate the adverse environmental and social impacts. Calcium Alginate-Graphene oxide (CA-GO) composite has been synthesized for the adsorption of heavy metals including Cr3+, Cu2+, and Cd2+ ions from tannery effluents. Graphene oxide is prepared from commercial graphite powder and reacted with sodium alginate and calcium chloride to form the beads of CA-GO composite. The developed composite was characterized by FTIR, elemental analysis, SEM, XRD analysis, and Raman spectroscopy. Moreover, the effect of pH, adsorbent dosage, contact time, and initial concentration of metal ions on the adsorption capacity were investigated through batch experiments. At a pH>3.0 (pHzpc), the carboxyl group of CA-GO was deprotonated to make the surface negatively charged and facilitate metal adsorption. The optimum pH and maximum adsorption capacity of CA-GO for removal of Cr(III), Cu(II), and Cd(II) were 4.5, 6.0, and 7.0, and 90.58, 108.57, and 134.77 mg g−1, respectively. The kinetics, adsorption isotherms, and thermodynamics were studied to determine the adsorption mechanism. The kinetic of adsorption adopted the second-order model. Thermodynamic parameter were calculated and the adsorption process was determined to be exothermic and spontaneous at room temperature. The developed composite has been efficaciously applied for the removal of metal ions and pollution from real tannery effluents.

Phosphorus‑carbon based hybrid electrodes for sodium ion batteries

In this study, commercial phosphorus powders were first subjected to mechanical ball-milling at varying times and reinforced with graphene oxide and multiwall carbon nanotubes to improve their electrochemical performances. All these processes were carried out by ball milling method to provide mechanical alloying of phosphorus. Subsequently, the crystallinity of the samples was analyzed by X-ray diffraction method, while the morphology of the samples was examined by field emission scanning electron microscopy. The main obstacles that inhibit the reversibility and the cyclic stability of red phosphorus are low electronic conductivity and huge volumetric expansion. Reinforcing amorphized phosphorous with multi-walled carbon nanotube and graphene oxide composites has presented similar initial capacity of 2100 mAh g−1. In addition, reversible capacity of multi-walled carbon nanotube and graphene oxide reinforced samples presented 370 mAh g−1 and 507 mAh g−1 after 250 cycles, respectively. Our results have shown that graphene oxide reinforced composites could be an alternative electrode material for sodium ion battery applications.

Phase evolution of nanocrystalline Mn-based oxides screened under different calcination temperatures using different precursors for proficient application in near infrared pigmentation

We examined how different calcination temperatures and precursors affect the formation of Mn-based oxides. The formation of these oxides was influenced by both the temperature (400–––1000 °C) and the type of precursors used (MnCl2·4H2O, MnCO3, MnO2, and KMnO4). When MnCl2·4H2O was calcined at 800 and 1000 °C/3h, we obtained pure tetragonal Mn3O4 phase materials. Calcining MnCO3 at 600 and 1000 °C resulted in cubic Mn2O3 and tetragonal Mn3O4 phase materials, respectively. Heating commercial MnO2 powder at 600 and 800 °C transformed it into cubic Mn2O3 phase materials. At 400 °C, the tetragonal MnO2 phase remained, but at 1000 °C, mixed Mn3O4 and Mn2O3 phases formed. Calcining KMnO4 at 1000 °C/3h led to the formation of δ-MnO2 materials. The morphological features of Mn2O3 and Mn3O4 materials exhibited different sizes and shapes, including nanostone-like, nanorod-like, and nanoflakes morphologies. The thermal analysis revealed significant differences in weight loss and thermal events, including exo and endothermic peaks. The Raman spectra and UV–Vis DRS measurements data support the formation of Mn-based oxides. The highest NIR reflectance for the various synthesized materials of Mn3O4 phase indicates a reflectance of 68 % in the solar region and 91 % in the color pigment region.

Development of spray‐dried oat milk powder with improved stability

AbstractBackground and ObjectivesOat milk is a plant‐based milk alternative and rich in various nutrients, however, the liquid product with a shorter shelf life limits its sales and consumption. This study is designed to develop an oat milk powder (OMP) using spray drying and improve the stability of reconstituted OMP by adding stabilizers.FindingsResults revealed that the optimal spray drying temperature was 160°C and the feed rate was 14 mL/min. The developed OMP showed higher bulk density compared to commercial soymilk powder. Furthermore, OMP maintained high contents of nutrients, including total phenol, β‐glucan, and various essential amino acids. The addition of stabilizers in OMP significantly decreased the turbidity and increased the pH stability, thermal stability, and freeze‐thaw stability of reconstituted OMP.ConclusionThe developed OMP product has abundant nutrients as well as stable physiochemical properties. Xanthan gum is the most effective stabilizer in improving the stability of reconstituted OMP across a wide range of pH and temperature.Significance and NoveltyThis study was the first to process oat milk into powder products and compare the effectiveness of different stabilizers in improving its stability. Our results suggest that OMP is a promising plant‐based beverage with stable physiochemical properties.

Safflower protein as a potential plant protein powder: optimization of extraction and spray-drying process parameters and determination of physicochemical and functional properties.

The research about sustainable and alternative plant protein sources has accelerated with the increasing need for protein. Safflower meal has a potential to be used in protein production due to its high protein content. This research aimed to produce an alternative plant-based protein powder using safflower meal. Both extraction and spray-drying parameters of safflower protein powder production were optimized using response surface methodology to achieve maximum yield. Moreover, the physicochemical and functional properties of safflower protein were determined and compared with those of commercial protein powders (soy, sunflower, pea, fava bean, and rice). The optimum extraction conditions were found to be 33.06:1 mL-1 g solvent-to-meal ratio, pH 11.00, 23.34 °C extraction temperature, and 30.86 min extraction time, which were achieved with a protein yield response of 75.21%. The highest powder yield (51.28%) was recorded for drying conditions of inlet air temperature of 160.11 °C, aspiration rate of 54.17 m3 h-1, and feed flow rate of 16.01 mL min-1. According to the amino acid profile of safflower protein, the glutamic acid content (14 475 mg (100 g)-1) was highest, while the methionine content (96 mg (100 g)-1) was lowest. Moreover, safflower protein can be regarded as a high-quality protein due to its high essential amino acid ratio (41.55%). The experiments showed that safflower protein had high solubility and good foam and emulsifying properties. Safflower protein could be a nutritional and functional protein source for the food industry. © 2024 Society of Chemical Industry.

Analysing the Composition of Commercial Turmeric Powder: Assessing Contaminants and Its Impacts Curcumin and Water-soluble Vitamins Levels

Aims: Turmeric, with its active component curcumin, has garnered global attention for its medicinal benefits, including anti-inflammatory and antioxidant properties. This study aimed to analyse turmeric powder obtained from the Greater Accra Metropolis for nutrients and contaminants. Study Design: Experimental. Place and Duration of Study: Entrance Pharmaceuticals, Accra for 6 months. Methodology: 22 samples from 10 different processing sites and open markets were tested using physical and chemical methods. HPLC identified curcumin, ascorbic acid, riboflavin, thiamine, and pyridoxine levels. An independent t-test was done to compare concentrations of these nutrients in the powdered turmeric samples from the two sources. Results: Assessment showed no yellow lead salts but 9.1% were adulterated with chalk, and 91% contained metanil yellow. Curcumin (2014.95 vs. 567.79), riboflavin (21.60 vs. 1.75), thiamine (14.75 vs. 0.65 mg/mL), pyridoxine (9.35 vs. 0.65 mg/mL), and ascorbic acid (0.00 vs. 101.60 mg/mL) were significantly higher (p<0.05) in processed samples than open market ones. Samples without adulterants had higher curcumin and micronutrient levels. Conclusion: Strengthening monitoring programs is crucial to tackling food adulteration concerns.

Functional food development using olive pomace phenolics and hydrogels

SummaryAlthough the health effects of olive phenolics, hydroxytyrosol (HX), are well known, their utilisation is not at the forefront of the phenolics market. Besides, 99% of olive phenolics are lost during olive oil production (2.2 million tons year−1). This study aims to develop a functional hydrogel for functional foods using commercial olive powder derived from olive mill wastewater and methylcellulose (MC). The final hydrogel recipe, a multi‐hydrocolloid recipe (MC and gelatine with low gelling temperature) based on minimum HX loss and acceptable sensory properties, was created by examining interactions of HX with salt, sugar, and citric acid in MC by a modified UPLC‐UV method and expert sensory panellists. Finally, two dairy bases were created for the hydrogel with the best aroma match, and consumer‐accepted dessert (72%) and appetiser (58%) providing the health claims of European Food Safety Authority (EFSA) (2 mg day−1 of HX) were produced. Moreover, a sample methodology has been developed.

The effectiveness of natural indigo/kaolinite composite powder in the development of latent fingermarks

BackgroundComposites are materials that have multiple phases and have attracted much attention as they are able to improve physical and chemical properties of an isolated material. In this sense, these composites are commonly used as key components for two purposes: coloring and improving the operational properties; besides that, they have alternative synthesis routes that respect the principles of green chemistry. Thus, this reports the development of a new composite using natural products, indigo and kaolinite, for application in papilloscopy as a new nontoxic fingermark developer.ResultsThe composite was obtained via green procedures and was characterized by spectroscopic and chromatographic techniques. Thus, to investigate the potential of the material as a fingermark developer, different techniques were applied such as depletion, aging, comparison with commercial powder, and development of latent fingermarks on different surfaces. Tests revealed that the composite presented good contrast and adhesion with the latent fingermarks, even after 15 days of deposition.ConclusionsThis study presents a natural indigo/kaolinite composite powder that showed similar or higher efficiency when compared to the commercial fingerprint powder and was able to develop identifiable natural and sebaceous fingermarks.Key points• A composite was formed from eco-friendly materials.• The composite formation follows the concepts of green chemistry and low cost.•The composite was applied as a latent fingermark developer.

Dynamic Gastrointestinal Digestion of Bovine, Caprine and Ovine Milk Reconstituted from Commercial Whole Milk Powders.

The global dairy market has been increasingly diversified with more dairy product offerings of milk products from different animal species. Meanwhile, milk powders remain the main exported dairy product format due to their ease of transportation. In this work, we studied the structural changes, protein hydrolysis and nutrient delivery during dynamic gastric digestion and small intestinal digestion of cow, goat and sheep milk reconstituted from commercial whole milk powders. The results show that the reconstituted milks digest similarly to processed fresh milk. The digestion behaviors of the three reconstituted ruminant milks are broadly similar (gastric coagulation, kinetics of gastric emptying of protein and fat and the high digestibility in the small intestine) with some differences, which are likely contributed by the processing history of the milk powders. The delivery of individual amino acids to the small intestine differed between the early and late stages of gastric digestion, which were primarily affected by the abundance of amino acids in caseins and whey proteins but also by the difference between milk types associated with their gastric coagulation behaviors. This work showed that powdered milk is similar to fresh processed milk in digestion behavior, and the inherent differences between ruminant milks can be modified by processing treatments.

Development of a novel UPLC approach to co-prediction of four active compounds in a multi-component pharmaceutical preparation

In this work, a new ultra-performance liquid chromatography method based on photodiode array detection (UPLC-PDA) was first developed for the quantitative analysis of the quaternary mixture of ascorbic acid (AA), paracetamol (PAR), caffeine (CAF) and chlorpheniramine maleate (CPA) in a commercial dosage form. The developed UPLC-PDA method offered a new possibility for the co-determination of four active ingredients in a drug combination with short run time and simple sample preparation. The successful chromatographic separation of the four drugs was performed using a Waters Acquity UPLC BEH C18 column (1.7 µm 2.1 × 100 mm) (Mildford, USA) and a mobile phase consisting of water (12 %), acetonitrile (13 %) and 0.1 M H3PO4 (75 %) at a flow rate of 0.25 mL/min. The validation of the proposed UPLC-PDA approach was verified by analyzing synthetic mixtures, inter- and intra-day experiments, and commercial powder samples and provided satisfactory results.

Preparation of BaAl2-xGaxSi2O8:Ce3+, M+ (Li, Na, K) blue-cyan phosphors based on charge compensation and cation substitution strategies and luminescence performance study

Highly efficient blue-cyan phosphors can fill the cyan gap in conventional white light-emitting diode (LED) devices to improve the spectral continuity while effectively increasing the white LED colour rendering index (Ra). In this study, Ba0·94Al2-xGaxSi2O8:0.06Ce3+, M+ (Li, Na, K, x = 0–0.8) blue-cyan phosphors with a feldspar structure were prepared by a high-temperature solid-phase method using charge compensation and cation substitution strategies. The barium (Ba) vacancy due to the charge-imbalance substitution of Ce3+ is compensated by the different charge compensators Li+, Na+, and K+. The charge compensators affect the luminescence performance of the samples, with the K+-compensated samples showing the greatest enhancement, with intensities up to 1.8 times that of the uncompensated samples. The cation substitution strategy using Ga3+ to partially replace Al3+ further improves the luminescence performance of the Ba0·94Al2Si2O8:0.06Ce3+, 0.04 K+ sample, and the excitation band is also improved. In this case, the luminescence intensity of the Ba0·94Al2Si2O8:0.06Ce3+ luminescent material is increased by a factor of 6, and a broadband blue-cyan phosphor with a full-width at half-maximum of 118 nm containing blue, cyan and green is obtained. The co-doping of charge compensators and partial cation substitution improved the luminescence performance of phosphors. The representative sample Ba0·94Al1.6Ga0.4Si2O8:0.06Ce3+, 0.04 K+ has a luminescence intensity at a temperature of 150 °C that is 83.2% of that at room temperature and good thermal stability. The combination of 365 nm near-ultraviolet (NUV) LED chips with Ba0·94Al1.6Ga0.4Si2O8:0.06Ce3+, 0.04 K+ and the commercial red powder (Ca, Sr)AlSiN3:Eu2+ yields a white LED device with an Ra of up to 93 and a correlated colour temperature (CCT) of 4825 K. These results show that the blue-cyan phosphor complements the cyan component while simplifying the manufacturing process of white LEDs.

Laser powder bed fusion of NdFeB and influence of powder bed heating on density and magnetic properties

Laser powder bed fusion (L-PBF) is an additive manufacturing technique that provides an opportunity to create complex NdFeB magnets, potentially enhancing their performance. L-PBF possesses its own processing challenges, such as porosity/cracks and thermal stresses due to rapid cooling. This study focused on optimizing the parameters and the use of elevated temperature (300–550 °C) powder bed heating to reduce defect generation. This paper includes a detailed process parameter investigation, which revealed samples with a maximum energy product, (BH)max, of 81 kJ/m3 (remanence, Br 0.72 T; coercivity, Hci 891 kA/m) without post/pretreatment, which are the highest (BH)max and Br for L-PBF-processed NdFeB commercial powder. It was observed that all the high-magnetism samples possessed high density, but not all the high-density samples possessed high magnetism. The SEM images and discussions are academically valuable since they clearly illustrate grain formation and morphology in the melt pool, areas where the literature provides limited discussion. Furthermore, this paper incorporates quantitative phase analyses, revealing that the magnetic properties increase with increasing volume fraction of the strong magnetic phase Nd2Fe14B. Another significant contribution of this paper is that it is the first study to investigate the effect of heated bed on L-PBF-NdFeB alloys. The density of the samples and Br can be improved with the use of elevated powder bed heating, while the Hc decreases. The (BH)max can also be improved from 55 to 84 kJ/m3 through elevated powder bed heating. The maximum magnetic properties obtained with the heated bed (400 °C) were as follows: Br, 0.76 T; Hci, 750 kA/m; and (BH)max, 84 kJ/m3.

Wet SPF: A wet powder suspension for the detection of latent fingermarks on the sticky side of adhesive tape for use in Seychelles

WET UCIO is an inexpensive carbon-based powder suspension, reportedly as effective as commercially available formulations for latent fingermark detection on the sticky side of adhesive tapes. However, the surfactant solution used in WET UCIO is not readily accessible outside Europe, limiting its use in Seychelles or other non-European jurisdictions. In this study, the UCIO formulation was modified based on a ‘frugal forensic’ approach, by replacing the surfactant solution with an in-house sodium dodecyl sulfate solution prepared in 5 % aqueous ethanol. A comparative assessment against Wetwop™ using eight different pressure-sensitive adhesive tapes found that the modified formulation was at least as effective as commercial powder suspension. Modifying this technique under the frugal forensic framework has enhanced its accessibility to other jurisdictions and is recommended for validation in Seychelles.

Low-crystallinity porous Ni2P2O7 nanowires with excellent CO2 capture ability for highly-efficient CO2 reduction

In this study, we prepared the porous Ni2P2O7 nanowires with low-crystallinity (LC-NPO) and high-crystallinity Ni2P2O7 nanosheets (HC-NPO), and employed them for the first time as catalyst in the CO2 photoreduction reaction. The photocatalytic performance of them was tested under the UV–Vis light irradiation and compared with the TiO2 commercial powder (P25). The CO2 photoreduction experiments shown that the LC-NPO had the highest ability than the HCNPO and the P25. Specifically, with triethanolamine (TEOA) as the sacrificial agent, LC-NPO achieved CO and CH4 yields of approximately 56.06 and 12.13 μmol·g−1 after 4 h UV–Vis light irradiation, which were 4.67 and 5.00 times of P25, respectively. The experimental results, and Density Functional Theory calculations proved that the unique porous nanowire structure enables LC-NPO to have a larger specific surface area, higher quantity of oxygen defects, and superior CO2 capture ability compared to HC-NPO. These features maybe the primary reasons for the excellent CO2 photoreduction ability. Besides, the photo-electrochemical characterizations revealed that the LC-NPO had the much superior photoelectrochemical properties than the HC-NPO, which was another reason for enhanced photocatalytic ability. In-situ FTIR and 13C isotope labeling experiments were used to monitor the CO2 reduction process, and finally a potential enhanced mechanism had been discussed.

Laser Powder Bed Fusion Processing of Low Cost CoCrFeNiMoxNby High Entropy Alloys with Promising High-Temperature Properties via In Situ Alloying Commercial Powders

A blend of only commercial powders, including Ni625, CoCrF75, and 316L, were used as the raw material for fabricating non-equiatomic CoCrFeNiMoxNby high entropy alloys (HEAs) through laser powder bed fusion (PBF-LB/M) via in situ alloying, instead of using pure elemental powders, thus reducing the raw materials cost. The rapid cooling inherent in the PBF-LB/M process facilitated the dissolution of Mo and Nb, resulting in a single FCC phase characterized by high relative densities. High-temperature tensile tests were conducted at room temperature, 700 °C, 800 °C, and 900 °C, revealing mechanical properties that surpassed those reported in existing HEA literature. The remarkable strength of the HEAs developed in this study primarily stemmed from the incorporation of Mo and Nb, leading to the precipitation of Mo and Nb-rich lave phases at elevated temperatures. While constraining elongation when confined to grain boundaries, these precipitates enhanced strength without compromising elongation when distributed throughout the matrix. This work is a feasibility study to explore the usage of commodity compositions from the market to develop HEAs using PBF-LB/M, which opens the possibility of using scraps to further the development of new materials. Consequently, this study presents a rapid and cost-effective approach for HEA development, improving efficiency and sidestepping the direct utilization of critical raw metals for sustainable manufacturing. Moreover, this work also underscores the outstanding mechanical performance of these HEAs at high temperatures, paving the way for the design of innovative alloys for future high-temperature applications.

Fabrication of nanocrystal forms of ᴅ-cycloserine and their application for transdermal and enteric drug delivery systems.

ᴅ-cycloserine (DCS), an FDA-approved medicine for the treatment of tuberculosis, is also a partial agonist at the glycine recognition site of N-methyl-ᴅ-aspartate (NMDA) receptor and has shown significant treatment efficacy for central nervous system (CNS) disorders including depression, schizophrenia, Alzheimer's disease, and post-traumatic stress disorder. The physicochemical properties of DCS, however, limit the options of formulation and medicinal applications of DCS, and warrants further investigation for the development of CNS therapeutics. Nanocrystals play an important role in pharmaceutic design and development. The properties of nanocrystals are remarkably different from their bulk material counterpart, attributed to the large surface-area-to-volume ratio which can improve the bioavailability. In this study, for the first time, DCS, a highly water-soluble compound, has formed nanocrystals and this was confirmed by scanning electronic microscopy and X-ray powder diffraction. Furthermore, DCS nanocrystals were applied to several formulations to test their stability and then to the in vitro Franz diffusion test with reservoir patch formulation as well as in vivo pharmacokinetics study with enteric capsules. We tested these formulations regarding their nanocrystal physical properties, size effect, and dissolution rate, respectively. We found that DCS nanocrystals showed good performance in the Franz diffusion test and rodent pharmacokinetic studies due to the nanoparticle size and faster dissolution as compared with the commercial DCS powder. These DCS nanocrystal formulations could offer a new approach for the development of an advanced drug delivery system for the treatment of CNS disorders.

Design of dual carbon encapsulated porous micron silicon composite with compact surface for enhanced reaction kinetics of lithium-ion battery anodes

Developing high-performance composites with fast charging and superior cycle life is paramount for lithium-ion batteries (LIBs). Herein, we synthesized a double-shell carbon-coated porous structure composite with a compact surface (P-Si@rGO@C) using low-cost commercial micron-sized silicon (Si) instead of nanoscale silicon. Results reveal that the unique P-Si@rGO@C features high adaptability to volume expansion, accelerates electron/ion transmission rate, and forms a stable solid electrolyte interphase (SEI) film. This phenomenon arises from the synergistic effect of abundant internal voids and an external double-layer carbon shell with a dense surface. Specifically, the P-Si@rGO@C anode exhibits a high initial coulombic efficiency (ICE) (88.0 %), impressive rate-capability (612.1 mAh/g at 2C), and exceptional long-term cyclability (972.2 mAh/g over 500 cycles at 0.5C). Further kinetic studies elucidate the diffusion-capacitance hybrid energy storage mechanism and reveal an improved Li+ diffusion coefficient (from 3.47 × 10-11 to 2.85 × 10-9 cm2 s-1). Ex-situ characterization confirms the crystal phase change of micron-sized Si and the formation of a stable LiF-rich SEI. Theoretical calculations support these findings by demonstrating an enhancement in the adsorption ability of Si to Li+ (from -0.89 to -0.97 eV) and a reduction in the energy migration barrier (from 0.35 to 0.18 eV). Additionally, practical LixSi powder is shown to increase the ICE of full cells from 67.4 % to 87.9 %. Furthermore, a pouch cell utilizing the prelithiated P-Si@rGO@C anode paired with LiNi1/3Co1/3Mn1/3O2 (NCM111) cathode delivers a high initial reversible capacity of 7.2 mAh and 76.8 % capacity retention after 100 cycles. This work provides insights into the application of commercial silicon-aluminum alloy powder in the anode of high-energy LIBs.