Dispersion State Research Articles

N-coordinated Ag sites on ordered mesoporous carbons for highly efficient electrolytic production of H2O2 in acidic electrolyte

N-coordinated Ag (Ag-Nx) sites embedded in ordered mesoporous carbon (Ag-Nx/C) were prepared by pyrolyzation of Ag-2, 2-bipyridine complexes in the confined channels of mesoporous SBA-15 silica. This nanocasting method allowed high dispersion state of Ag-Nx sites on carbons with ordered mesoporous channels and higher specific surface area. Ag-Nx/C was found to be very active electrocatalyst for two-electron oxygen reduction reaction (2e- ORR) in 0.1 M HClO4 acidic electrolyte. The bulk electrolytic production for hydrogen peroxides (H2O2) could be achieved with a high production rate of 1.67 mol h−1 gcat−1 together with high electrolysis Faraday efficiency of about 93%. Ag-Nx/C also revealed better acid-resistant durability during H2O2 electrolysis production. This work provided an efficient and durable Ag-Nx/C electrocatalyst for electrolytic H2O2 production in acids.

Waterborne 2-component polyurethane coatings based on acrylic polyols with secondary alcohols

We report the effects of increasing the molecular weight of a secondary alcohol-based polyol in a two-component waterborne polyurethane (2 K-WB-PUR) formulation. The system consists of an acrylic polyol latex and a water-dispersible polyisocyanate (hmPIC, Basonat HW1000 from BASF). The polyols investigated incorporated hydroxypropyl methacrylate as a comonomer to introduce the secondary –OH groups, in contrast to typical polyols which have primary -OH groups. Three molecular weights of this polyol were prepared (Mn ≈ 5100, Ð = 2.4; 10,300, Ð = 2.7; or 12,900 g/mol, Ð = 3.6) with a uniform Tg (∼20 °C) and hydrodynamic diameter (dh) ≈ 120 nm. The polyol and polyisocyanate were mixed with a molar NCO:OH ratio of 1.3:1. The particle size of the mixed dispersion was monitored by dynamic light scattering. The 5 K sample remained stable in dispersion over 7 days whereas the higher molecular weight formulations flocculated after 1 day. Fourier Transform Infrared (FTIR) measurements revealed that all NCO groups were consumed within 15–23 h for all dispersed samples. Fluorescence resonance energy transfer (FRET) experiments were carried out on samples in the dispersed state as well as on films formed from these dispersions. Very little molecular level mixing was observed in the dispersed phase for the samples. In the films, a large extent of mixing was observed in the 5 K sample whereas the extents of mixing for the higher molecular weight samples were reduced. The FTIR measurements recorded as the films formed showed that the NCO consumption in the 5 K film (t1/2 = 56 h) was comparable to an analogous 2 K-WB-PUR formulation based on a 5 K primary alcohol from a previous study. Surprisingly, the NCO consumption in the higher molecular weight samples was faster (t1/2 = 31, 32 h). We found that the composition of the resulting films formed from higher molecular weight polyols contained a greater relative ratio of polyurea to polyurethane.

Dispersion state analysis in hot melt extruded, highly drug-loaded 3D printing filaments applying Raman microscopy

Abstract Objectives Highly drug-loaded polymer formulations are favorable intermediates in pharmaceutical applications, for example, for the individualized production of medicines via 3D printing with the maximum flexibility regarding dose strength and drug combination in a single dosage form. However, high-disperse drug loads are challenging for the process itself and the (intermediate) product properties, making the knowledge about the dispersion state of the drug particles achieved by the production process helpful to overcome such challenges. Methods Therefore, a novel dispersion state analysis technique based on scanning Raman microscopy is proposed in the present study and applied to HPMC filaments loaded with 20 wt%, 40 wt%, and 60 wt% theophylline. The qualitative and quantitative evaluations of the scans were correlated to melt viscosities, process data, and mechanical properties of the filaments. Key findings The analyses revealed not only an increasing particle size reduction with increasing drug load and thus increasing viscosity and mechanical energy input. The particle size reduction also caused a change in the filaments’ mechanical properties from elastic ductile to rigid brittle. Furthermore, an alignment of the elongated drug particles with the frozen three-dimensional flow pattern of the extruder and not only with the extrusion direction was elucidated. Conclusions Therefore, the necessity to investigate the dispersion state further is highlighted for future studies on highly drug-loaded polymer formulations, providing a novel measuring technique applicable to challenging pharmaceutical formulations.

Therapeutic potential and chemo-morphological characterization of silver nanoparticles synthesized using aqueous extracts of Monarda citriodora Cerv. ex Lag.

In present study, bioreduction of silver nitrate to silver nanoparticles was carried out using leaf extracts of Monarda citriodora plant. Different reaction parameters viz: inorganic silver salt (AgNO3) concentration, monarda extract concentration, pH and reaction time were varied to optimize the conditions for maximum recovery of silver nanoparticles. Monarda citriodora plant could efficiently bio-reduce silver ions. The efficiency of process increased with increasing salt concentration. Maximum recovery of AgNO3 was attained at 5 mM concentration with 5% concentration of MC leaf extract. The mixture incubated for 24 h at pH 8 gave maximum recovery. The images from scanning electron microscope (SEM) confirmed the dispersed state of silver nanoparticles. The energy-dispersive spectroscopy (EDX) graphs depicted that silver nanoparticles comprised 91.97% of silver mixed with some groups like N and Al acting as capping agents. Presence of organic groups like –OH was confirmed by Fourier transform infrared spectroscopy (FTIR) graphs. The x-ray diffractometer (XRD) peaks corroborated with presence of silver in mixture. Antimicrobial and anti-oxidant activities of nanoparticles were studied. From the results it was observed that silver nano-particles are potential agonistics to many microbial strains and also have efficient free radical scavenging properties when compared with ascorbic acid.

Enhancing Latex Compounds and Vulcanized Rubber Properties with Silver Nanoparticles

The production process of latex products requires the preparation of latex compounds by mixing latex with chemicals in a dispersion state. This experiment investigated the influence of added zinc oxide and silver nanoparticles on the properties of latex compounds and vulcanized rubber. It was found that increasing the amount of zinc oxide in the rubber compound resulted in a rise in the viscosity of the latex over the storage period. Increasing the zinc oxide content also led to a higher degree of crosslink noticed by a faster chloroform number determination of the vulcanization level and the opposite effect on the swell value of the rubber film with reduced swelling. The amount of 2.0 phr of ZnO as an activator gave the highest value of the tensile strength. The increasing amount of silver nanoparticles caused a decrease in the viscosity and exhibited a slower chloroform number with a decrease in the swelling of the rubber film. The amount of silver nanoparticles in the study period (0.0010-0.0022 phr) had little effect on mechanical properties but a significant effect on antibacterial activity. The 0.0010 phr of silver nanoparticles showed sufficient potential in inhibiting Staphylococcus aureus and Escherichia coli.

In-depth investigation of how carbon nanofiller dispersion affects microcellular foaming behavior in poly(butylene succinate) nanocomposites

This study explores the impact of carbon nanotubes (CNTs) dispersion on the microcellular foaming characteristics of poly(butylene succinate) (PBS) matrices. Two distinct dispersion methods, primary (PD) and secondary (SD), were employed to fabricate PBS/CNT nanocomposites, resulting in different filler dispersion states. The PD technique involves the conventional method of direct melt blending PBS with CNTs, while the SD technique adopts a more advanced strategy by integrating the Pickering emulsion template with melt blending, achieving finer CNTs distribution within the PBS matrix. The results reveal that the SD technique leads to significantly more uniform distribution of CNTs, which in turn enhances the melt strength and crystallization of the polymer matrix, thereby broadening the window for microcellular foaming. Notably, foams developed through the SD method exhibited a decrease in cell size to 10.4 μm and an increase in cell density to 1.8×1010 cells·cm‐3. Moreover, this uniform distribution of CNTs contributed to superior cell stability and an increase in compressive strength to 14.0 MPa. These findings highlight the pivotal role of nanofiller dispersion in determining foam properties and establish foundational knowledge for designing PBS foams with consistent and uniform cell structures. Such advancements are crucial for enhancing the applicability and performance of PBS-based materials across a spectrum of industries.

Reversible Intrapore Redox Cycling of Platinum in Platinum-Ion-Exchanged HZSM-5 Catalysts.

Isolated platinum(II) ions anchored at acid sites in the pores of zeolite HZSM-5, initially introduced by aqueous ion exchange, were reduced to form platinum nanoparticles that are stably dispersed with a narrow size distribution (1.3 ± 0.4 nm in average diameter). The nanoparticles were confined in reservoirs within the porous zeolite particles, as shown by electron beam tomography and the shape-selective catalysis of alkene hydrogenation. When the nanoparticles were oxidatively fragmented in dry air at elevated temperature, platinum returned to its initial in-pore atomically dispersed state with a charge of +2, as shown previously by X-ray absorption spectroscopy. The results determine the conditions under which platinum is retained within the pores of HZSM-5 particles during redox cycles that are characteristic of the reductive conditions of catalyst operation and the oxidative conditions of catalyst regeneration.

Taming the terminological tempest in invasion science.

Standardised terminology in science is important for clarity of interpretation and communication. In invasion science - a dynamic and rapidly evolving discipline - the proliferation of technical terminology has lacked a standardised framework for its development. The result is a convoluted and inconsistent usage of terminology, with various discrepancies in descriptions of damage and interventions. A standardised framework is therefore needed for a clear, universally applicable, and consistent terminology to promote more effective communication across researchers, stakeholders, and policymakers. Inconsistencies in terminology stem from the exponential increase in scientific publications on the patterns and processes of biological invasions authored by experts from various disciplines and countries since the 1990s, as well as publications by legislators and policymakers focusing on practical applications, regulations, and management of resources. Aligning and standardising terminology across stakeholders remains a challenge in invasion science. Here, we review and evaluate the multiple terms used in invasion science (e.g. 'non-native', 'alien', 'invasive' or 'invader', 'exotic', 'non-indigenous', 'naturalised', 'pest') to propose a more simplified and standardised terminology. The streamlined framework we propose and translate into 28 other languages is based on the terms (i) 'non-native', denoting species transported beyond their natural biogeographic range, (ii) 'established non-native', i.e. those non-native species that have established self-sustaining populations in their new location(s) in the wild, and (iii) 'invasive non-native' - populations of established non-native species that have recently spread or are spreading rapidly in their invaded range actively or passively with or without human mediation. We also highlight the importance of conceptualising 'spread' for classifying invasiveness and 'impact' for management. Finally, we propose a protocol for classifying populations based on (i) dispersal mechanism, (ii) species origin, (iii) population status, and (iv) impact. Collectively and without introducing new terminology, the framework that we present aims to facilitate effective communication and collaboration in invasion science and management of non-native species.

Ex situ and in situ studies on structural features of Pt/Ce0.75Zr0.25O2 catalyst for water gas shift reaction

Pt/Ce1-xZrxO2 catalysts have shown high activity in water gas shift (WGS) reaction, but their structural organization has been studied insufficiently. This work represents a detailed structural study on the supported Pt species and the metal/support interface in a 5 wt% Pt/Ce0.75Zr0.25O2 catalyst in the initial state, after reductive activation, and after WGS reaction in H2-enriched reformate-simulating mixture. A wide range of methods was used: ex situ and in situ X-ray diffraction (XRD) studies, high resolution transmission electron microscopy (HRTEM), X-ray atomic pair distribution function (PDF) method, pseudo in situ X-ray photoelectron spectroscopy (XPS), hydrogen temperature-programmed reduction (H2-TPR). The Ce0.75Zr0.25O2 mixed oxide was shown to provide a highly dispersed state of Pt species. XPS revealed that the initial catalyst contains Pt2+species. PDF analysis allowed us to propose the structure of ultrafine PtO particles and to elucidate the metal-support interaction with fixation of Pt ions on the support surface. In situ XRD, pseudo in situ XPS, and H2-TPR studies revealed the reduction of ultrafine PtO particles in H2 atmosphere at low temperatures (20–90°С) with the formation of metallic Pt0 particles and simultaneous partial reduction of the support surface due to the hydrogen spillover. Catalytic tests of the as-prepared and poisoned with chlorine 5wt% Pt/Ce0.75Zr0.25O2 catalysts in the WGS reaction showed an important role of the oxygen vacancies in the oxide support as active sites. These findings contribute to the understanding catalytic performance of Pt/Ce1-xZrxO2 systems.

Processing–microstructure–fracture toughness relationships in PP/EPDM/SiO2 blend‐nanocomposites: Effect of mixing sequence

AbstractThis study investigates the mechanical properties and fracture behavior of polypropylene (PP)‐based blend‐nanocomposites comprising 30 wt.% ethylene–propylene–diene monomer (EPDM) and 5 wt.% SiO2 nanoparticles. Different mixing sequences were employed to prepare the nanocomposites, and the resulting morphology development and dispersion states of modifiers were analyzed. Mechanical performance of the nanocomposites was evaluated through quasi‐static and high‐speed dynamic fracture tests. The dispersion and distribution of SiO2 nanoparticles within the nanocomposites were significantly influenced by the mixing protocol. In impact fracture tests, the presence of nanoparticles exhibited a beneficial efffect on fracture energy, demonstrating a synergistic toughening effect of the soft EPDM and rigid SiO2 particles. Conversely, adverse effects were observed in quasi‐static tests. Essential work of fracture (EWF) parameters indicated an increase in the yielding component and a decrease in the necking‐to‐tearing component with SiO2 incorporation into the PP/EPDM blends. During impact loadings, the highest improvement in crack propagation resistance was observed in nanocomposites with nanoparticles localized around the rubbery domains forming a network‐like structure of EPDM/SiO2‐nanoparticles. Morphologies where rubber domains and nanoparticles were separately distributed in the PP matrix resulted in the lowest fracture parameters. Energy dissipation mechanisms were elucidated, revealing multiple void formation followed by matrix shear yielding as the primary source under both quasi‐static and impact fracture conditions. In the latter case, stress‐concentrating percolated structures in the PP matrix facilitated the nucleation of dilatational bands evolving into highly stretched void‐fibrillar structures upon further loading. These findings contribute valuable insights into tailoring nanocomposite morphologies for enhanced mechanical performance in different loading scenarios.Highlights Fracture behavior of PP/EPDM/SiO2 ternary systems was evaluated by EWF methodology and Izod impact test. Rubber particles surrounded by silica nanoparticles led to a percolated morphology and as a result to superior impact resistance. EWF parameters were mostly controlled by the tearing‐related parts regardless of phase morphology. The impact toughness was mainly controlled by the dispersion and distribution characteristics of the SiO2 nanoparticles.

Methane dehydroaromatization (MDA) on VOx/HZSM-5 catalysts

In this study, the methane dehydroaromatization (MDA) on vanadium oxide (VOx)-based catalysts was investigated. Using various catalyst supports, VOx/HZSM-5 exhibited the highest MDA activity. In MDA using VOx/HZSM-5, an induction period was observed. Raman spectroscopy and XPS analysis indicated that V2O5 species result in the highly dispersed state by the contact with CH4. X-ray absorption fine structure analysis suggested the formation of VC species. Such structural changes lead to the induction period for the MDA reaction. Based on the effect of the catalyst support and the aromatization reaction of ethylene, we propose a mechanism in which methane forms ethylene on the vanadium catalyst, and ethylene is then aromatized with the aid of the acid sites and micropore structure of HZSM-5. Additionally, the effect of hydrogen co-feeding on the MDA reaction was investigated, which revealed that catalyst deactivation due to coke formation was suppressed in the presence of hydrogen.

Spartina alterniflora invasion decouples multiple elements in coastal wetland soils

Deciphering the biogeochemical coupling of multiple elements in soils could better mechanistic understanding of ecosystem stability response to the alien invasion. The coupling of 45 elements in soils from wetlands covered by Spartina alterniflora (Sa) was compared with that in soils covered by native Phragmites australis (Pa) in coastal regions of China. Results showed that S. alterniflora invasion not only significantly reshaped geochemical enrichment and dispersion states, but also decoupled the coupling of multiple elements in soils compared with Pa. Atomic mass emerged as the primary factor governing the coupling of multiple elements, of which a significantly positive correlation exhibited between atomic mass with elemental coupling in Pa, but no such relation was observed in SaThe coupling of lighter elements was more susceptible to and generally enhanced by the invasion of S. alterniflora compared to the heavier, of which carbon, iron (Fe), and cadmium (Cd) had the highest susceptibility. Besides atomic mass, biological processes (represented by soil organic carbon, nitrogen, phosphorus, and sulfur), interactions between sea and land (represented by salinity and pH), and their combination explained 17 %, 10 %, and 13 % variation in the coupling of multiple elements, respectively. The present work confirmed that S. alterniflora invasion was the important factor driving soil multi-element cycling and covariation in coastal wetlands.

Ambrosia beetles adjust dispersal preferences to their degree of exhaustion

Abstract Delayed dispersal of sexually mature offspring is a fundamental component of cooperative breeding in fungus farming ambrosia beetles. These beetles dwell in logs of recently deceased trees, where female offspring postpone reproduction and invest in alloparental care before dispersing to found a new nest. The wood quality affects investment of adult offspring in alloparental care and hence the breeder's reproductive success. This raises the question of whether dispersing breeders choose habitats strategically to optimise breeding prospects and modulate their offspring's helping propensity. To answer this question, here we tested experimentally whether during dispersal, Xyleborinus saxesenii Ratzeburg (Coleoptera: Scolytinae) uses olfactory cues emitted by mutualistic or pathogenic fungi as an information source on prospective habitat quality. As the mutualistic relationship between the fungi and beetles is obligate, fungus scent should provide a reliable source of information on habitat quality, indicating prior successful colonisation by conspecifics. We found no evidence for direct pathogen avoidance. However, the beetles clearly responded to scent of their mutualistic fungi, dependent on dispersal state. At the onset of dispersal, females avoided the scent of fungus mutualists, whereas they were attracted to them after being exhausted by an experimentally prolonged dispersal time. The observed change of preference during dispersal suggests that beetles freshly emerging from their home gallery may choose pristine habitat by avoiding mutualist scent. This might help to avoid competition with conspecifics and potential pathogen and parasite cross contamination. Exhausted beetles, however, may accept these risks and choose successfully colonised habitat to avoid starvation. State‐dependent adjustment of habitat preferences may be exhibited also in other economically impactful bark and ambrosia beetles, which prompts further study of the olfactory cues used by these beetles during dispersal.

Molecular architectures of iron complexes for oxygen reduction catalysis—Activity enhancement by hydroxide ions coupling

Developing cost-effective and high-performance electrocatalysts for oxygen reduction reaction (ORR) is critical for clean energy generation. Here, we propose an approach to the synthesis of iron phthalocyanine nanotubes (FePc NTs) as a highly active and selective electrocatalyst for ORR. The performance is significantly superior to FePc in randomly aggregated and molecularly dispersed states, as well as the commercial Pt/C catalyst. When FePc NTs are anchored on graphene, the resulting architecture shifts the ORR potentials above the redox potentials of Fe2+/3+ sites. This does not obey the redox-mediated mechanism operative on conventional FePc with a Fe2+-N moiety serving as the active sites. Pourbaix analysis shows that the redox of Fe2+/3+ sites couples with HO- ions transfer, forming a HO-Fe3+-N moiety serving as the ORR active sites under the turnover condition. The chemisorption of ORR intermediates is appropriately weakened on the HO-Fe3+-N moiety compared to the Fe2+-N state and thus is intrinsically more ORR active.

Effect of Ultrasonic Treatment on the Physicochemical Properties of Bovine Plasma Protein-Carboxymethyl Cellulose Composite Gel.

In order to improve the stability of bovine plasma protein-carboxymethyl cellulose composite gels and to expand the utilization of animal by-product resources, this study investigated the impact of different ultrasound powers (300, 400, 500, 600, and 700 W) and ultrasound times (0, 10, 20, 30, and 40 min) on the functional properties, secondary structure and intermolecular forces of bovine plasma protein-carboxymethyl cellulose composite gel. The results showed that moderate ultrasonication resulted in the enhancement of gel strength, water holding capacity and thermal stability of the composite gels, the disruption of hydrogen bonding and hydrophobic interactions between gel molecules, the alteration and unfolding of the internal structure of the gels, and the stabilization of the dispersion state by electrostatic repulsive forces between the protein particles. The content of α-helices, β-turns, and β-sheets increased and the content of random curls decreased after sonication (p < 0.05). In summary, appropriate ultrasound power and time can significantly improve the functional and structural properties of composite gels. It was found that controlling the thermal aggregation behavior of composite gels by adjusting the ultrasonic power and time is an effective strategy to enable the optimization of composite gel texture and water retention properties.

Ruthenium supported on silicate and aluminosilicate mesoporous materials applied to selective sugar hydrogenation: Xylose to xylitol

A series of ruthenium-based catalysts supported on a set of silicate and aluminosilicate mesoporous molecular sieves was synthesized and tested in xylose hydrogenation. The materials were characterized in terms of morphology, textural properties, acidity, as well as ruthenium loading, dispersion, and oxidation state. In general, the aluminosilicates-based catalysts displayed a higher activity compared to their respective silicate supports, which can be ascribed to a higher Ru content and dispersion, enhanced by a higher acidity. The most active synthesized catalyst (Ru/Al-MCM-4) displayed an improved performance compared to a commercial Ru/C catalyst due to a better xylitol selectivity. Two modelling approaches were implemented to describe the kinetic rate. The first model was based on the hypothesis that xylose molecules and hydrogen are adsorbed in different active sites on the catalyst surface, while the second model supposes the formation of an intermediate on the catalyst surface that reacts to form xylitol. Both models gave a very good description of the experimental data.

Rational design of cationic starch with high purification performance and insight into the working mechanism

The utilization of starch to treat sewage that received widespread attention has become one of the promising ways to purify water due to the advantages of low cost and biodegradability. However, the poor purification capacity for wastewater and difficult liquid phase dispersion of natural starch severely hindered its application in wastewater treatment and limited the development of starch materials. Hence, a series of cationic starches with different particle sizes were fabricated by controlling the acidification time and combining starch with N-2,3-epoxy-propyl trimethyl ammonium chloride to improve the dispersion and purification effect of starch in water. Acid hydrolysis could destroy the spatial structure of starch, which improved the etherification property to enhance the purification property of starch to different pollutants and the dispersed stable state in water. The maximum adsorption capacities of the optimal functional agents were 43.2 mg/g (methyl orange), and 236.8 mg/g (acid black) and the optimal penetration rate of the treated kaolin solution was 94.6%. The working behavior of cationic starch could be composed of rapid, stable, and equilibrium stages, and the working process of HS-g-GTA conformed to the pseudo-second-order dynamic model. This work provides a simple and low-energy pretreatment method for preparing cationic starch, which has important application value in removing anionic substances from wastewater.

Design and Study of Novel Composites Based on EPDM Rubber Containing Bismuth (III) Oxide and Graphene Nanoplatelets for Gamma Radiation Shielding.

The mechanical, thermal and gamma radiation attenuation properties of ethylene-propylene-diene monomer (EPDM)-based composites containing graphene nanoplatelets (GNs) and bismuth (III) oxide nanoparticles (B) were investigated. The use of polyethylene glycol (PEG) as a compatibilizer to improve the dispersion of the fillers was also investigated. The results showed that the combined use of these fillers resulted in a drastic increase in mechanical properties, reaching 123% and 83% of tensile strength and elongation at break, respectively, compared to those of EPDM. In contrast, the addition of PEG to composites containing EPDM GNs and B resulted in composites with lower values of mechanical properties compared to the EPDM/B/GN-based composite. However, the presence of PEG leads to obtaining a composite (EPDM/B/GNP) with a mass attenuation coefficient to gamma radiation (137Cs, 662 keV) superior to that composite without PEG. In addition, the composite EPDM, B and PEG exhibited an elongation at break 153% superior to unfilled EPDM. Moreover, the binary filler system consisting of 100 phr of bismuth (III) oxide and 10 phr of GN leads to reaching 61% of the linear damping coefficient of the EPDM composite compared to that value of the unfilled EPDM. The study of the morphology and the state of filler dispersion in the polymer matrix, obtained using scanning electron microscopy and energy-dispersive X-ray spectroscopy, respectively, provides a useful background for understanding the factors affecting the gamma radiation attenuation properties. Finally, the results also indicated that by adjusting the formulation, it is possible to tune the mechanical and thermal properties of EPDM composites reinforced with bismuth oxide and graphene nanoplatelets.

Direct observation and elemental analysis of material nanoparticles in solution using scanning electron-assisted dielectric microscopy and EDS

High-resolution observation and elemental analysis of various particles in solution are important in the fields of materials, analytical chemistry, and industrial applications. Analysis of slurries of raw materials is essential for the development of highly functional materials. Recently, we have developed an SEM-based scanning electron assisted dielectric microscope (SE-ADM), which can directly observe biological samples and organic materials in aqueous solutions. Here, we have developed an SE-ADM system with the addition of energy-dispersive x-ray spectrometry that enables direct observation and elemental analysis of nanoparticles in solution. Using this system, we were able to directly observe and conduct elemental analysis of ceramic slurries and to clarify the dispersion state of alumina particles in solution, the distribution of binder, and the bonding state of silica and magnesium particles. Furthermore, our system can be applied to diverse liquid samples across a broad range of scientific and industrial fields, for example, nanotubes, organic specimens, batteries, and catalytic materials.

Solid Dispersions of Genistein via Solvent Rotary Evaporation for Improving Solubility, Bioavailability, and Amelioration Effect in HFD-Induced Obesity Mice.

Genistein (GEN) is an active pharmaceutical ingredient that presents the challenges of poor water solubility and low oral bioavailability. To tackle these challenges, a GEN solid dispersion was prepared by solvent rotary evaporation using polyvinylpyrrolidone K30 (PVP K30) as a carrier. The optimal formulation was determined by drug loading efficiency and in vitro release. The physical state of the solid dispersion was characterized by DSC, XRD, SEM and FT-IR. And the results of the in vitro release study indicate that the drug release of SD (1:7) increased 482-fold that of pure GEN at 60 min. Following oral administration to rats, the Cmax and AUC0-24 of SD (1:7) was increased 6.86- and 2.06-fold to that of pure GEN. The adipose fat index and body weight of the SD (1:7) group were significantly lower than those of the GEN group (p < 0.05). Meanwhile, the levels of TC and TG in the serum were significantly decreased in the SD (1:7) group compared with the GEN group (p < 0.05). All experiments revealed that solid dispersion could be a promising formulation approach to improve the dissolution rate, oral bioavailability, and effect on the reduction of lipid accumulation in high-fat diet-induced obesity mice.