Ostwald Ripening Research Articles

Growth and shrinkage of tissue sheets on substrates: buds, buckles, and pores

Abstract Many tissues take the form of thin sheets, being only a single cell thick, but millions of cells wide. 
These tissue sheets can bend and buckle in the third dimension. In this work, we investigated the growth and shrinkage of suspended and supported tissue sheets using particle-based simulations. We construct a minimum model, combining particle-based tissue growth and meshless membrane models, to simulate the growth of tissue sheets with mechanical feedback. Free suspended growing tissues exhibit wrinkling when growth is sufficiently fast. Conversely, tissues on a substrate form buds when the adhesion to the substrate is weak and/or when the friction with the substrate is strong. These buds undergo a membrane-mediated attraction and subsequently fuse. The complete detachment of tissues from the substrate and straight buckled bump formation are also obtained at very weak adhesion and/or fast growth rates. In the tissue shrinkage, tissue pores grow via Ostwald ripening and coalescence. The reported dynamics can also be applied in research on the detachment dynamics of different tissues with weakened adhesion.

Kinetic features and mechanism of scorodite formation via multivalent iron source from arsenic-bearing solution

Arsenic-bearing wastes from non-ferrous metallurgy exhibit poor stability during long-term storage, and are transferred as pollutants to the atmosphere and groundwater, thereby, threatening human health and ecological security. Immobilising arsenic as scorodite crystals via a multivalent iron source (Fe(OH)3-FeSO4·7 H2O) is one effective approach for controlling arsenic pollution. However, the kinetic features and mechanisms of this method have not yet been revealed, thereby, necessitating further research. Herein, the kinetics of scorodite generation influenced by the initial pH, Fe/As ratio, Fe(III)/Fe(II) ratio, and reaction temperature were investigated. Prominent features included variations in the minimum pH, oxidation–reduction potential (ORP) platform, Fe/As ratio (1.0), and the delay or advance of scorodite generation. The complicated mechanism of scorodite formation can be divided into coordinated polymerisation, acidic Fe(OH)3 dissolution, polymer oxidation, Fe(II) oxidation, and scorodite crystallisation. The fast coordinated polymerisation of precursors ([Fe(H2O)4(H2AsO4)]nn+) in stage I resulted in a decrease in pH; Fe(OH)3@scorodite and Fe(H2O)2AsO4 basic units were formed via the oxidation of ionic Fe(III) in stage II. Furthermore, regular octahedral scorodite was generated from two sources: the crystallisation of Fe(H2O)2AsO4 basic units and Ostwald ripening of flaky scorodite from Fe(III)–As(V) precipitates at stage III. The Fe(II) in the polymers was mainly oxidised by ferric ions generated from the oxidation of ferrous ions via dissolved O2 from the oxygen gas. Fe(II) ions as carriers for transferring electrons from O2 to polymers. Scorodite formation was controlled by the oxidation of Fe(II) by oxygen gas. Overall, this study provides guidance for the effective immobilisation of arsenic wastes into scorodite via multivalent iron sources to eliminate arsenic pollution.

Impact of hydrophilic substances on Ostwald ripening in emulsions stabilized by varied hydrophilic group surfactants

This study investigated the impact of water-soluble substances on Ostwald ripening in emulsions stabilized by surfactants with different head groups (Brij S20 and Tween 60). Adding ≥20% (w/w) corn oil to the oil phase effectively inhibited Ostwald ripening of n-decane emulsions due to compositional ripening. The presence of glucose, maltose, or glycerol in the aqueous phase of the emulsions decreased the Ostwald ripening rate, regardless of emulsifier type. However, the impact of propylene glycol depended on emulsifier type, accelerating Ostwald ripening in Brij S20-stabilized emulsions but having little effect in Tween 60-stabilized emulsions. This effect was mainly attributed to the ability of propylene glycol to alter interfacial characteristics. When emulsions were fabricated with a mixture of n-decane and corn oil, glucose and maltose were still effective in inhibiting Ostwald ripening, but glycerol lost its ability. These results have important implications for formulating emulsion-based delivery systems with enhanced shelf life.

Stabilization of gels and emulsions in the ternary water/eugenol/poloxamer 407-system: Physicochemical characterization and potential application as encapsulation platforms

The ternary system water/eugenol/poloxamer 407 can form a variety of phases that are strongly influenced by the mixture composition and the thermal history of the system. In this study, we investigated the stabilization of emulsion and gel-like systems in which eugenol is encapsulated in a poloxamer 407 matrix. Our results reveal the complex interplay between poloxamer 407 and eugenol compositions in the stabilization single-phase systems at 25ºC. Increasing concentrations of poloxamer were found to incorporate higher amounts of eugenol into emulsion-like dispersions, effectively preventing coalescence and Ostwald ripening. However, high concentrations of poloxamer 407 induced gelation of these dispersions, resulting in eugenol-loaded poloxamer 407 gels. The thermal annealing of the emulsions at 65°C for 1 h followed by equilibration at room temperature allows the extension of the compositional range for the formation of homogeneous single-phase systems providing a strategy to modulate the phase diagram of the ternary system. Additionally, the encapsulation of hydrophobic pesticides in gel-like matrices was investigated, showing uniform distribution and consistent loading capacity (approximately 0.70 % w/w) across different pesticides which may contribute to facilitate the environmental distribution and efficacy of the encapsulated molecules. This research highlights the potential of eugenol/poloxamer 407-based systems as an environmentally friendly platform for the encapsulation and delivery of hydrophobic active molecules, offering a versatile solution for various applications.

Ostwald-Ripening Induced Interfacial Protection Layer Boosts 1,000,000-Cycled Hydronium-Ion Battery.

Collapsing and degradation of active materials caused by the electrode/electrolyte interface instability in aqueous batteries are one of the main obstacles that mitigate the capacity. Herein by reversing the notorious side reactions include the loss and dissolution of electrode materials: as we applied Ostwald ripening (OR) in the electrochemical cycling of a copper hexacyanoferrate electrode in a hydronium-ion batteries, the dissolved Cu and Fe ions undergo a crystallization process that creates a stable interface layer of cross-linked cubes on the electrode surface. The layer exposed the low-index crystal planes (100) and (110) through OR-induced electrode particle growth, supplemented by vacancy-ordered (100) superlattices that facilitated ion migration. Our design stabilized the electrode-electrolyte interface considerably, achieving a cycle life of one million cycles with capacity retention of 91.6%, and a capacity retention of 91.7% after 3000 cycles for a full battery.

Ostwald‐Ripening Induced Interfacial Protection Layer Boosts 1,000,000‐Cycled Hydronium‐Ion Battery

Collapsing and degradation of active materials caused by the electrode/electrolyte interface instability in aqueous batteries are one of the main obstacles that mitigate the capacity. Herein by reversing the notorious side reactions include the loss and dissolution of electrode materials: as we applied Ostwald ripening (OR) in the electrochemical cycling of a copper hexacyanoferrate electrode in a hydronium‐ion batteries, the dissolved Cu and Fe ions undergo a crystallization process that creates a stable interface layer of cross‐linked cubes on the electrode surface. The layer exposed the low‐index crystal planes (100) and (110) through OR‐induced electrode particle growth, supplemented by vacancy‐ordered (100) superlattices that facilitated ion migration. Our design stabilized the electrode–electrolyte interface considerably, achieving a cycle life of one million cycles with capacity retention of 91.6%, and a capacity retention of 91.7% after 3000 cycles for a full battery.

Simulation of Localized Stress Impact on Solidification Pattern during Plasma Cladding of WC Particles in Nickel-Based Alloys by Phase-Field Method

As materials science continues to advance, the correlation between microstructure and macroscopic properties has garnered growing interest for optimizing and predicting material performance under various operating conditions. The phase-field method has emerged as a crucial tool for investigating the interplay between microstructural characteristics and internal material properties. In this study, we propose a phase-field approach to couple two-phase growth with stress–strain elastic energy at the mesoscale, enabling the simulation of local stress effects on the solidified structure during the plasma cladding of WC particles and nickel-based alloys. This model offers a more precise prediction of microstructural evolution influenced by stress. Initially, the phase field of WC-Ni binary alloys was modeled, followed by simulations of actual local stress conditions and their impacts on WC particles and nickel-based alloys with ProCAST and finite element analysis software. The results indicate that increased stress reduces grain boundary migration, decelerates WC particle dissolution and diffusion, and diminishes the formation of reaction layers and Ostwald ripening. Furthermore, experimental validation corroborated that the model’s predictions were consistent with the observed microstructural evolution of WC particles and nickel-based alloy composites.

Study on Attenuation Mechanism and Durability Improvement of Platinum-Carbon Catalysts for Proton Exchange Membrane Fuel Cells

The relationship between Pt particle size and activity and durability of Pt/C electrocatalysts on rotating disk electrodes is established and the results show that Pt/C electrocatalysts with particle size over 3.5 nm have excellent resistance to Pt particle decay and carbon corrosion. Further, the research results on the mechanism of Pt particle decay and carbon corrosion show that the Pt particle attenuation is composed of 80% Ostwald ripening and 20% particle agglomeration, and the carbon corrosion is affected by the catalytic action of Pt particles. Therefore, the above results show that regulating the Pt particle size to 3.5–4.0 nm can improve the durability of Pt/C electrocatalysts on RDE. To verify the accuracy of this conclusion and determine the optimal particle size range in practical application, single cells with 5 × 5 cm2 is assembled to evaluate the performance and durability of cathode Pt/C electrocatalysts under H2/air. The results show that cathode Pt/C electrocatalysts with particle size between 3.5 nm and 3.8 nm have high single cell performance (2.3 A cm−2@0.65 V) and durability (A loss of 15 mV@0.8 A cm−2 after 30000 cycles). These findings reveal the attenuation mechanism of Pt/C electrocatalysts and provide ideas for the development of high-durability Pt-based electrocatalysts for practical applications.

Reaction-Driven Migration Dynamics of Nano-Metal Particles Unraveled by Quantitative Electron Microscopies.

The stability of supported nano-metal catalysts holds significant importance in both scientific and economic practice, beyond the long pursuit of enhanced activity. While previous efforts have concentrated on augmenting the interaction between nano-metals and carriers, in the thermodynamic macro-perspective, to achieve optimized repression upon particle migration coalescence and Ostwald ripening, nevertheless, the microscale kinetics of migrating catalyst particles driven by the reaction remains unknown. In this work, the migration of nano-copper particles is investigated during hydrogen oxidation reaction by utilizing high spatiotemporal resolution of environmental transmission electron microscopy. It is shown that there exists a delicate correlation between the migration dynamics of nano-copper particles and the evolution of asymmetrically distributed Cu and Cu2O phases over the particle surface. It is found that the interplay of reduction and oxidation near the surface areas filled with Cu and Cu2O phases can facilitate the pressure gradient, which drives the migration of nano-particles. A driving force model is therefore established which is capable of qualitatively explaining the influences of reaction conditions such as temperature and hydrogen-to-oxygen ratio on the reaction-driven particle migration. This work adds a potential yet critical perspective to understanding particle migration and thus the nano-metal catalyst particle sintering in heterogeneous catalysis.

MnFe Prussian Blue Analogue Open Cages for Sodium-Ion Batteries: Simultaneous Evolution of Structure, Morphology, and Energy Storage Properties.

Prussian blue analogues (PBAs) exhibiting hollow morphologies have garnered considerable attention owing to their remarkable electrochemical properties. In this study, a one-pot strategy is proposed for the synthesis of MnFe PBA open cages. The materials are subsequently employed as cathode electrode in sodium-ion batteries (SIBs). The simultaneous evolution of structure, morphology, and performance during the synthesis process is investigated. The findings reveal substantial structural modifications as the reaction time is prolonged. The manganese content in the samples diminishes considerably, while the potassium content experiences an increase. This compositional variation is accompanied by a significant change in the spin state of the transition metal ions. These structural transformations trigger the occurrence of the Kirkendall effect and Oswald ripening, culminating in a profound alteration of the morphology of MnFe PBA. Moreover, the shifts in spin states give rise to distinct changes in their charge-discharge profiles and redox potentials. Furthermore, an exploration of the formation conditions of the samples and their variations before and after cycling is conducted. This study offers valuable insights into the intricate relationship between the structure, morphology, and electrochemical performance of MnFe PBA, paving the way for further optimizations in this promising class of materials for energy storage applications.

Geological conditions and fluid flow history that lead to the development of large clastic dykes in basins: A case study from Kushiro, Japan

AbstractLarge clastic dykes (the Harutori‐Taro and Harutori‐Jiro dykes) and smaller dykes are exposed in the underground Kushiro Coal Mine (KCM), Japan. This study examines these dykes as a case study to investigate the geological conditions and fluid flow history that lead to the development of large clastic dykes in basins. The composition of the dykes indicates the Beppo and/or Harutori formations as their parent unit. Crystallite size distribution (CSD) analysis reveals Ostwald ripening of the kaolinite in the kaolinitised feldspar from the dykes, suggesting stagnant conditions in the parent unit before the dyke was formed. In contrast, smectite CSDs and the high carbonate content of the dykes suggest that large volumes of fluid flowed through the dykes along the established hydraulic gradient, which was triggered by the breaking of the upper seal. The isotopic and chemical compositions of the calcite and aragonite in the dykes, with moderate siderite and rhodochrosite content, indicate the fluid was a warm (>30°C) mixture of freshwater and saltwater, which was transferred from deeper levels of the parent unit towards the crest of an anticline. Immediately after sand injection, the semi‐closed system of the parent unit near the root of the large dyke was transformed into a major flow channel for overpressurised fluids. Subsequently, a large volume of fluid flowed along the vertical conduit (or dyke) over a long period of time (>1 Myr), which removed fluid from a widespread area (i.e., several hundred square kilometres) of the basin. The results show that thin parent units, poor lateral continuity of the upper seal, and spatially heterogeneous overpressurisation do not preclude the formation of large dykes.

Formation and evolution of nanobubbles in CH4-H2O-Alcohol system: Insight into the effect of alcohol chain length from molecular dynamics simulations

Nanobubbles (NBs) which are gas filled cavities of nanometre dimensions present in liquids attracted increasing attention in the recent years due to their application in various fields such as chemistry, biology, medicine etc. An important aspect of NB research is the study of effect of additives on formation and evolution of these bubbles. The present study examined by applying molecular dynamics simulations, the formation and evolution of methane NBs in the CH4-H2O-Alcohol system, which is known to form during alcohol induced dissociation of CH4 hydrates in the natural gas extraction process. The effect of alcohol type and concentration on NB formation and evolution was examined through simulations of CH4-H2O-CH3OH, CH4-H2O-C2H5OH and CH4-H2O-nC3H7OH systems. The study revealed that increase in both concentration and the alkyl chain length of alcohols promoted NB formation. Alcohol molecules are found to enhance NB nucleation through accumulation near the NB-liquid interface resulting in a decrease in the surface tension (γ) at the interface. These effects become more pronounced as the alkyl chain length increases which explains the enhanced NB formation in systems containing nC3H7OH and C2H5OH compared to those containing CH3OH. The mechanism of formation and evolution of NBs is found to significantly depend on the type of alcohol present. NBs are found to nucleate at multiple locations in the systems containing nC3H7OH and C2H5OH which eventually coalesce to form a single large stable NB. In the presence of NBs which vary significantly in size, bubble growth was also found to occur through Ostwald ripening which involves transfer of CH4 from smaller NB to the larger one. In contrast, in the CH4-H2O-CH3OH system, primarily a single NB nucleated which grew in size through absorption of CH4 molecules dissolved in the liquid, rather than through coalescence or Ostwald ripening. The observed influence of alcohol type on the process of NB evolution is explained by examining the influence of alkyl chain length on γ and diffusivity of CH4 molecules. Due to the role of NBs on methane hydrate regeneration from the hydrate melt, we examined the influence of NB in the CH4-H2O-Alcohol system on the organization of water molecules (HSWs) present in the hydration shell of dissolved CH4. The value of F4 order parameter of HSWs and the number of hydrogen bonded water rings in the hydration shell of CH4 were analysed. The value of F4 order parameter indicate that the hydrophobic alkyl chain of alcohol induced hydrate like arrangement of HSWs, which is more pronounced in the case of alcohol with longer alkyl chain. However, alcohol molecules are also found to dislodge HSWs around CH4 resulting in a decrease in the number of water rings around dissolved CH4 which is not conducive to hydrate formation. These observations are consistent with the reported dual effect of alcohol on hydrate formation with alcohol promoting hydrate formation at low concentrations and inhibiting at high concentrations.

A study of the spinodal decomposition of AgC[sbnd]u alloy films using in situ transmission electron microscopy

We performed in situ transmission electron microscopy (TEM) investigations to understand spinodal decomposition in AgCu alloy thin films. The decomposition of a homogeneous nanocrystalline morphology into a heterogeneous two-phase structure when annealed in situ from room temperature to 400 °C was investigated with different imaging modes in the TEM. These studies reveal phase transformation proceeds in stages: between 180 and 200 °C, onset of phase separation via spinodal decomposition is observed. Then, prominent phase separation occurs between 200 and 250 °C with minimal grain growth. Next, between 250 and 300 °C, grain growth primarily occurs via coalescence, with no apparent phase separation. From 300 to 350 °C, we observe significant phase separation and Ostwald Ripening. Finally, between 350 and 400 °C, further coarsening occurs via coalescence. STEM-HAADF mode reveals the onset of phase separation from domains as small as 5 nm and these results are also supported by electron diffraction and compositional mapping.

Interplay of condensate material properties and chromatin heterogeneity governs nuclear condensate ripening.

Nuclear condensates play many important roles in chromatin functions, but how cells regulate their nucleation and growth within the complex nuclear environment is not well understood. Here, we report how condensate properties and chromatin mechanics dictate condensate growth dynamics in the nucleus. We induced condensates with distinct properties using different proteins in human cell nuclei and monitored their growth. We revealed two key physical mechanisms that underlie droplet growth: diffusion-driven or ripening-dominated growth. To explain the experimental observations, we developed a quantitative theory that uncovers the mechanical role of chromatin and condensate material properties in regulating condensate growth in a heterogeneous environment. By fitting our theory to experimental data, we find that condensate surface tension is critical in determining whether condensates undergo elastic or Ostwald ripening. Our model also predicts that chromatin heterogeneity can influence condensate nucleation and growth, which we validated by experimentally perturbing the chromatin organization and controlling condensate nucleation. By combining quantitative experimentation with theoretical modeling, our work elucidates how condensate surface tension and chromatin heterogeneity govern nuclear condensate ripening, implying that cells can control both condensate properties and the chromatin organization to regulate condensate growth in the nucleus.

Pore engineering of Porous Materials: Effects and Applications.

Porous materials, characterized by their controllable pore size, high specific surface area, and controlled space functionality, have become cross-scale structures with microenvironment effects and multiple functions and have gained tremendous attention in the fields of catalysis, energy storage, and biomedicine. They have evolved from initial nanopores to multiscale pore-cavity designs with yolk-shell, multishells, or asymmetric structures, such as bottle-shaped, multichambered, and branching architectures. Various synthesis strategies have been developed for the interfacial engineering of porous structures, including bottom-up approaches by using liquid-liquid or liquid-solid interfaces "templating" and top-down approaches toward chemical tailoring of polymers with different cross-linking degrees, as well as interface transformation using the Oswald ripening, Kirkendall effect, or atomic diffusion and rearrangement methods. These techniques permit the design of functional porous materials with diverse microenvironment effects, such as the pore size effect, pore enrichment effect, pore isolation and synergistic effect, and pore local field enhancement effect, for enhanced applications. In this review, we delve into the bottom-up and top-down interfacial-oriented synthesis approaches of porous structures with advanced structures and microenvironment effects. We also discuss the recent progress in the applications of these collaborative effects and structure-activity relationships in the areas of catalysis, energy storage, electrochemical conversion, and biomedicine. Finally, we outline the persisting obstacles and prospective avenues in terms of controlled synthesis and functionalization of porous engineering. The perspectives proposed in this paper may contribute to promote wider applications in various interdisciplinary fields within the confined dimensions of porous structures.

Stabilization of Metal Alloy Nanocatalysts by Encapsulation with a Metal Oxide

The threat of climate change motivates us to reduce our reliance on fossil fuels and transition to renewable energy infrastructure. Many clean energy technologies including hydrogen fuel cells, direct methanol fuel cells, and water electrolyzers utilize electrocatalysts to generate electricity from chemical energy or vice versa. One direction for increasing the catalytic performance and tolerance to contaminants of the catalyst layers is the development of metal alloy-based catalysts. For instance, ruthenium (Ru) can be alloyed with platinum (Pt) to increase the tolerance of Pt to carbon monoxide, a contaminant that can be found in hydrogen fuel. However, metal alloy catalysts have an additional route for degradation beyond the well-established Ostwald ripening, coalescence, and dissolution mechanisms that are an issue for nanoparticle electrocatalysts. Harsh fuel cell conditions can lead to a separation of the two metals that were originally alloyed in the nanocatalyst and, as a result, this leads to a loss in catalytic performance and tolerance to contaminants.1 This project focuses on the durability of alloyed PtRu electrocatalysts, which facilitate the methanol oxidation reaction in a direct methanol fuel cell and the hydrogen oxidation reaction in a hydrogen fuel cell.This project explored an encapsulation of electrodeposited PtRu nanoparticle catalysts with a porous niobium oxide as a method to stabilize the PtRu alloy. Niobium oxide was chosen due to its high corrosion resistance and previous studies showing its stabilization of Ru.2 PtRu alloyed nanoparticles were synthesized via electrodeposition on a glassy carbon electrode substrate and subsequently encapsulated by an electrophoretic deposition method adapted from Jha et al.3 The morphology and composition of the catalyst and encapsulating layer were characterized by scanning and transmission electron microscopy, energy dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, Raman spectroscopy, and optical microscopy. The activity and durability of pristine and encapsulated PtRu catalysts were evaluated by cyclic voltammetry, linear sweep voltammetry, chronoamperometry, and electrochemical impedance spectroscopy. Carbon monoxide stripping and the double layer capacitance methods were used to study changes in the electrochemically active surface area before and after deposition of the niobium oxide. Access to the electrocatalyst surfaces through the encapsulating layer was maximized by the addition of surfactants and through tuning the potentials applied during the deposition of the niobium oxide as a means to improve its porosity. The niobium oxide was shown to improve the stability of the PtRu alloy and maintain the CO tolerance of the alloy well beyond that of the un-encapsulated catalyst. The stabilization of PtRu imparted by the encapsulation of niobium oxide herein is promising for the stabilization of alloyed nanoparticle catalysts towards a wide range of electrocatalytic applications. Yang, Z.; Yu, X.; Zhang, Q. RSC Adv., 2016, 6, 114014-114018.Jha, G.; Tran, T.; Qiao, S.; Ziegler, J. M.; Ogata, A. F.; Dai, S.; Xu, M.; Thai, M. L.; Chandran, G. T.; Pan, X.; Penner, R. M. Mater. 2018, 30, 6549-6558.

Formation and coarsening of epitaxially-supported metal nanoclusters

This mini-review describes developments over the last ∼30 years in characterizing the nucleation & growth of epitaxially-supported metal nanoclusters (NCs) or islands during vapor deposition, as well as their post-deposition coarsening. A beyond-mean-field treatment for homogeneous nucleation & growth corrects the deficiencies of traditional treatments in describing, e.g., the island size distribution, but also necessitates consideration of the spatial distribution of islands and their capture zones. We discuss advances in modeling capabilities, including those based upon on an ab-initio level treatment of periphery diffusion kinetics, for description of the non-equilibrium growth shapes of these NCs, focusing on 2D NCs. For post-deposition coarsening of arrays of NCs, there is generally a competition between Ostwald Ripening (OR) and Smoluchowski Ripening (SR). SR is also known as Particle Migration & Coalescence. For 2D NCs in homoepitaxial systems, conventional OR is observed on pristine fcc(111) surfaces, dramatically enhanced OR in the presence of even trace amounts of chalcogens for Cu(111) and Ag(111), and anomalous OR on anisotropic fcc(110) surfaces. The unexpected discovery of SR for fcc(100) homoepitaxial systems prompted extensive analysis of the underlying diffusivities of 2D NCs as a function of size, as well as of NC coalescence dynamics. A comprehensive understanding of these processes is now available. Self-assembly of 3D NCs during deposition, issues related to heterogeneous nucleation, directed assembly, NC growth structure selection, and coarsening are addressed. For SR of 3D epitaxial NCs, recent insights into the size-dependence of diffusivity are described.

Growth Mechanisms of Amorphous Nanoparticles in Solution and During Heat Drying

The purpose of this study was twofold: to identify the growth mechanisms of amorphous nanoparticles in solution and during the drying process at high temperatures, and to guide the process condition and stabilizer selection for amorphous nanoparticle formulations. In contrast to nanocrystals that are mostly mechanically robust, amorphous nanoparticles tend to undergo deformation under stress. As a result, development of a stable formulation and evaluation of the drying process for re-dispersible amorphous nanoparticles presents considerable challenges. Although amorphous nanoparticles have stability issues, they have several pros in terms of production, high monodispersity, and diverse applications in drug delivery. In this study, amorphous nanoparticles were prepared via liquid-liquid phase separation, and their growth mechanisms were investigated both in solution and during the drying process. In solution, particles were found to be susceptible to flocculation, crystallization, coalescence, and Ostwald ripening, with coalescence being a preliminary step providing the driving force for Ostwald ripening. However, during the heat drying process, coalescence and crystallization were found to be the primary mechanisms for particle growth, with Ostwald ripening being negligible due to reduced molecular mobility. The glass transition temperature (Tg) of these amorphous nanoparticles was found to be a crucial factor both in solution and during the drying process. At temperatures < Tg, particles remained in a rigid, glassy state thereby inhibiting coalescence, whereas at or above Tg, particles transition from glassy to rubbery state, making them more susceptible to deformation and coalescence. The mechanistic understanding of particle growth from this study can also be extended to the stabilization of other types of soft nanoparticles.

Late-stage microstructures in Chang’E-5 basalt and implications for the evolution of lunar ferrobasalt

Abstract This study investigates silicate liquid immiscibility (SLI) microstructures in the Chang’E-5 (CE-5) lunar ferrobasalt sample, the youngest recovered mare basalt (ca. ~2.0 Ga). Employing advanced high-resolution imaging techniques and chemical analysis, we examined a subophitic fragment, revealing two distinct types of microstructures indicative of multi-stage SLI events. The first type is observed in the mesostasis pockets and exhibits both “sieve” and “maze” textures, where the Si-K rich glassy phases are interconnected with Fe-rich minerals, e.g., fayalite. This type of microstructure, similar to previous observations in Apollo and Luna samples, is the product of a stable SLI event. The second type is characterized by K-free but high-Si melt inclusions occurring as emulsions in the rims of plagioclase. The entrapment of these emulsions followed a metastable SLI event, with the Fe-rich liquids serving as precursors to subsequent stable SLI processes. Additionally, the Fe-rich droplets within the emulsions underwent coarsening via Ostwald ripening, a phenomenon in which smaller particles in solution dissolve and deposit on larger particles. Our simulation of this coarsening process suggests a duration of at least 15-32 days for the SLI processes, alongside a slow cooling rate (&amp;lt; 0.3 °C/hour) of the late-stage CE-5 lava. We propose that metastable SLI may have influenced the effusive signature of the CE-5 lava flow during its late-stage evolution. The metastable SLI process can potentially lead to the formation of various phases during the late-stage evolution of lunar ferrobasaltic magmas, thereby contributing to the diversity of lunar rock types.

An interesting phase transition in polyamide 6/nitrile rubber blend induced by temperature and pressure and its effect on tribological performance

AbstractThe preparation of high‐performance rubber‐plastic blending elastomers has always been a research hotspot in the field of petroleum equipment. The two‐phase separation structure of the blend determines the macroscopic properties of the materials. It is of great significance to deeply explore the influence of processing technology on the two‐phase separation structure. In this paper, polyamide 6 (PA6)/nitrile rubber blends were prepared via the melt–compounding method. To meet the requirements of oil production and oil transport equipment, we investigated systematically the mechanical properties of the specimens exposed to different environments. The oil resistance and high‐temperature resistance of the blends were enhanced considerably with the addition of PA6. The temperature and pressure fields induced a novel transition from particle into fibrous phase based on Ostwald's ripening. However, this brand new transformation showed no benefits to the improvement of the frictional performance. Meanwhile, the relationship between aggregate structure and mechanical performance was demonstrated from the aspects of crystallization behavior and phase morphology.