Desorption Of Particles Research Articles

Nonequilibrium cluster-cluster aggregation in the presence of anchoring sites.

Nonequilibrium cluster-cluster aggregation of particles diffusing in or at the cell membrane has been hypothesized to lead to domains of finite size in different biological contexts, such as lipid rafts, cell adhesion complexes, or postsynaptic domains in neurons. In this scenario, the desorption of particles balances a continuous flux to the membrane, imposing a cutoff on possible aggregate sizes and giving rise to a stationary size distribution. Here, we investigate the case of nonequilibrium cluster-cluster aggregation in two dimensions where diffusing particles and/or clusters remain fixed in space at specific anchoring sites, which should be particularly relevant for synapses but may also be present in other biological or physical systems. Using an effective mean-field description of the concentration field around anchored clusters, we derive an expression for their average size as a function of parameters such as the anchoring site density. We furthermore propose and solve appropriate rate equationsthat allow us to predict the size distributions of both diffusing and fixed clusters. We confirm our results with particle-based simulations and discuss potential implications for biological and physical systems.

Bimetallic NiFe nanoparticles deposited on hollow glass microspheres (HGMs) of various sizes for the catalytic hydrogenation of CO2

The composites based on hollow glass microspheres (HGMs) decorated with nanoparticles of nickel and iron oxides were prepared from the nitrate solutions with ultrasound treatment. Further exposition of these composites in a hydrogen-helium flow leads to the formation of nanosized bimetallic particles of Ni(80)Fe(20) (number in the brackets is estimated as wt%) that are effective in the catalytic reaction of CO2 hydrogenation to methane. Investigation of CO2 conversion was carried out under gas chromatographic control, and methane yield was evaluated for composites with 20 and 60 wt% of grafted bimetallic mass. The TPD MS method was used to study the processes of desorption of particles involved in the mechanism of methane formation. Textural and structural characteristics of as-prepared and post-reacted composites were examined using low-temperature nitrogen adsorption and X-ray diffraction methods.

Microscopic Mechanism and Percolation Model of Dynamic Deposition of Elemental Sulfur Particles in Acidic Gas Reservoirs.

The dissolution of elemental sulfur in acidic gas leads to its precipitation as gas pressure decreases, thereby causing potential damage to the formation due to the deposition of sulfur particles. Previous sulfur deposition prediction models often relied on the solubility of sulfur in acidic gas and the stress state of sulfur particles to determine the occurrence of deposition, thus establishing predictive models. However, in the presence of complex geological conditions, the multiphase flow through porous media and the adsorption of particles on pore throat walls can also influence sulfur particle deposition to some degree. It is well known that sulfur particle deposition during gas reservoir development exhibits instability, with multiple factors influencing the deposited sulfur particles. Particularly noteworthy is the influence of airflow velocity, which can resuspend sulfur particles that are physically adsorbed on pore throat surfaces, thereby reintegrating them into the gas phase. Additionally, the dynamic deposition of larger sulfur particles involves a dynamic process. This study elucidates the dynamic process of sulfur deposition by considering the diverse transport dynamics of sulfur particles. Physical adsorption and desorption behaviors of sulfur particles are determined based on variations in reservoir conditions. The desorption status of sulfur particles with different particle sizes within the formation is established by evaluating the equilibrium between the force exerted on the pore throat wall and the suspension force generated by gas flow. The critical conditions for sulfur deposition in Yuanba gas reservoir were obtained by substituting on-site parameters into calculations. Moreover, a mathematical model is proposed to describe the dynamic deposition and migration of sulfur particles, adopting principles from continuous porous media porous flow theory, fluid flow mass conservation, as well as sulfur particle desorption and migration. The formulated model is solved, and its resulting solution process and outcomes hold significant implications for numerical simulation and predictive assessment of the development impact on gas reservoirs, particularly in later stages.

The Seasonal Effect of Coastal Current and Upwelling on the Dynamics of Dissolved Organic Matter in the Northwestern South China Sea

AbstractPrevious studies have primarily focused on the impact of human activities on coastal dissolved organic matter (DOM) cycles, while neglecting the role of dynamic processes. This limits our comprehensive understanding of the dynamic processes of coastal DOM, particularly in coastal waters affected by multiple dynamic processes. In this study, the dynamics of DOM in the northwestern South China Sea (SCS) were investigated using DOM‐related parameters and a three end‐member mixing model, which accounted for the effects of coastal currents and upwelling during the spring, summer, and winter seasons. Our results demonstrated that the net addition of DOM was predominantly observed in the nearshore during all seasons, owing to strong coastal currents that induced phytoplankton production and particle desorption. However, owing to weaker coastal currents and upwelling in spring and winter, DOM removal induced by decomposition was observed in the western offshore area. This observation can be attributed to the abundance of microorganisms in spring and increased vertical water mixing in winter. Conversely, in summer, stronger upwelling provided more bio‐refractory DOM, limiting its decomposition, whereas stronger coastal currents stimulated productivity and particle desorption, resulting in the net addition of DOM during this period. In the eastern offshore area, DOM decomposition was the primary mechanism for eliminating DOM owing to weak or absent coastal currents and upwelling. Our study revealed that DOM decomposition is widespread in the coastal regions of the northwestern SCS and that stronger coastal currents and upwelling facilitate the net addition of DOM.

Analysis of damage mechanisms and controlling factors of fine particle migration in unconsolidated sandstone reservoirs based on reservoir classification

AbstractParticle migration in oil and gas reservoirs is a common phenomenon in the process of oil and gas development, and is considered to be an important reason for the damage of reservoir permeability and the reduction of oil and gas productivity. The mechanism of this phenomenon includes the desorption, migration, and precipitation of particles, which eventually clogs the throat and causes reservoir damage. Therefore, it is necessary to accurately characterize the complex mechanism of particle migration and identify the main controlling factors of particle migration, which is very important for efficient oilfield development and plugging solution. First, the reservoir types are divided into three types and the pore structure models of different types of reservoirs are established. Then, computational fluid dynamics and discrete element coupling method numerical simulation and microscopic visualization of pore throat structure model were combined, to characterize the rules of particles and migration, and analyze the main controlling factors. Finally, a typical model of particle migration and clogging is established. The results show that particle size/throat and particle concentration are the key factors affecting particle plugging, and particle migration has the least effect on the permeability of Type I reservoir and the greatest damage to Type III reservoir. According to the mechanical and hydrodynamic behavior of particles in porous media, three mechanisms and six modes of particle plugging are proposed.

Field study on the uptake pathways and their contributions to the accumulation of organophosphate esters, phthalates, and polycyclic aromatic hydrocarbons in upland rice

Plant uptake of organic contaminants generally occurs through either root, gas-phase foliar, or particle-phase foliar uptake. Understanding these pathways is essential for food-system practitioners to reduce human exposures, and to clean contaminated-sites with phytoremediation. Herein, we conducted a field-based experiment using an improved specific exposure chamber to elucidate the uptake pathways of organophosphate esters, phthalates, and polycyclic aromatic compounds, and quantitatively assessed their contributions to organic contaminant accumulations in field-grown rice. For most target compounds, all three uptake pathways (root, foliar gas, and foliar particle uptakes) contributed substantially to the overall contaminant burden in rice. Compounds with lower octanol–water partition coefficients (Kow) were more readily translocated from roots to leaves, and compounds with higher octanol−air partition coefficients (Koa) tended to enter rice leaves mostly through particle deposition. Most compounds were mostly stored in the inner leaves (55.3–98.2 %), whereas the relatively volatile compounds were more readily absorbed by the waxy layer and then transferred to the inner leaves. Air particle desorption was a key process regulating foliar uptake of low-volatility compounds. The results can help us to better understand and predict the environmental fate of those contaminants, and develop more effective management strategies for reducing their human exposure through food ingestion.

Preparation of porous materials by ultrasound-intensified acid leaching of high-carbon component in coal gasification fine slag

Coal gasification fine slag is one of the by-products from clean and efficient utilization of coal, and its resource utilization is extremely urgent. In this work, a high carbon fraction with a fixed carbon content higher than 60% was obtained by simple sieving of gasification fine slag, from which a porous material was prepared by ultrasonic acid leaching method. The adsorption performance of porous materials, being used as treatment of radioactive iodine in nuclear wastewater, is characterized by iodine adsorption value. The effects of ultrasound time, ultrasound power, acid concentration, and temperature on the iodine adsorption performance and compositional structure of the porous materials were systematically investigated by combining the results of SEM, BET, XRD, and FT-IR. The mechanisms of ultrasound-enhanced acid leaching on compositional structure of residual carbon and migration and transformation laws of the ash constituents were explored and summarized. The results show that the porous material prepared under conditions of acid concentration of 4 mol/L, acid immersion temperature of 50 °C, ultrasonic power of 210 W, and ultrasonic time of 1.5 h has the best iodine adsorption performance of 468.53 mg/g, with a specific surface area of 474.97 m2/g, and possesses a rich pore structure with predominant mesopores. The order of each factor on the iodine adsorption performance is: sonication time > acid concentration > sonication power > acid immersion temperature. The mechanism of ultrasonic enhanced acid leaching is that ultrasonic cavitation and mechanical wave action firstly enhance dissociation of carbon-ash adherent particles, thus making desorption of ash particles blocked in pore channels of the gasification slag to increase its connectivity; secondly, lead to generation of cracks on surface of the carbon and ash particles to enhance accessibility of inorganic components inside the carbon particles; and thirdly, enhance the acid leaching process by increasing mass transfer rate to strengthen leaching effect of inorganic components in the gasification slag.

Variation in chemical composition and volatility of oxygenated organic aerosol in different rural, urban, and mountain environments

Abstract. The apparent volatility of atmospheric organic aerosol (OA) particles is determined by their chemical composition and environmental conditions (e.g., ambient temperature). A quantitative, experimental assessment of volatility and the respective importance of these two factors remains challenging, especially in ambient measurements. We present molecular composition and volatility of oxygenated OA (OOA) particles in different rural, urban, and mountain environments (including Chacaltaya, Bolivia; Alabama, US; Hyytiälä, Finland; Stuttgart and Karlsruhe, Germany; and Delhi, India) based on deployments of a filter inlet for gases and aerosols coupled to a high-resolution time-of-flight chemical ionization mass spectrometer (FIGAERO-CIMS). We find on average larger carbon numbers (nC​​​​​​​) and lower oxygen-to-carbon (O : C) ratios at the urban sites (nC: 9.8 ± 0.7; O : C: 0.76 ± 0.03; average ±1 standard deviation) compared to the rural (nC: 8.8 ± 0.6; O : C: 0.80 ± 0.05) and mountain stations (nC: 8.1 ± 0.8; O : C: 0.91 ± 0.07), indicative of different emission sources and chemistry. Compounds containing only carbon, hydrogen, and oxygen atoms (CHO) contribute the most to the total OOA mass at the rural sites (79.9 ± 5.2 %), in accordance with their proximity to forested areas (66.2 ± 5.5 % at the mountain sites and 72.6 ± 4.3 % at the urban sites). The largest contribution of nitrogen-containing compounds (CHON) is found at the urban stations (27.1 ± 4.3 %), consistent with their higher NOx levels. Moreover, we parametrize OOA volatility (saturation mass concentrations, Csat) using molecular composition information and compare it with the bulk apparent volatility derived from thermal desorption of the OOA particles within the FIGAERO. We find differences in Csat values of up to ∼ 3 orders of magnitude and variation in thermal desorption profiles (thermograms) across different locations and systems. From our study, we draw the general conclusion that environmental conditions (e.g., ambient temperature) do not directly affect OOA apparent volatility but rather indirectly by influencing the sources and chemistry of the environment and thus the chemical composition. The comprehensive dataset provides results that show the complex thermodynamics and chemistry of OOA and their changes during its lifetime in the atmosphere. We conclude that generally the chemical description of OOA suffices to predict its apparent volatility, at least qualitatively. Our study thus provides new insights that will help guide choices of, e.g., descriptions of OOA volatility in different model frameworks such as air quality models and cloud parcel models.

Modelling selenium behavior in aquatic systems: a review of status, challenges, and opportunities.

Selenium (Se) is an essential element for aquatic organisms as well as humans. It can be toxic to organisms depending on its concentration and chemical speciation; thus, considerable efforts have been made to unravel the biogeochemical cycling of Se in aquatic systems. Mathematical models provide an important tool to better understand the fate of Se in different environment compartments. However, a comprehensive review of modeling Se in aquatic systems with current challenges and opportunities is missing. To fill this gap, we firstly summarize the processes governing Se cycling in aquatic systems, including particle adsorption and desorption, diffusion, biological uptake, redox reactions, and volatilization. Then, we critically review the available models, identifying the compartments modelled, environmental factors considered, and the Se species and geochemical processes used in each model, providing an assessment of their advantages and limitations. Data availability for modeling studies is investigated, highlighting how to better quantify the redox reactions, estimate of Se loadings, and mass balance. For the modeling of Se cycling in aquatic systems, the ability of the models to link sources to biota concentrations under a range of hydrodynamic conditions and with mechanistic representations of transport, transformation, and uptake processes is required. The majority of the current models can conduct this task; however, to better present the uptake processes of Se in the food web, two-way coupling of the Se cycling model with a food web model is recommended.

Characteristics of Ultrafine Bubbles (Bulk Nanobubbles) and Their Application to Particle-Related Technology

Ultrafine bubbles (bulk nanobubbles), small bubbles less than 1µm in diameter, have attracted academic and industrial attention because of their numerous advantages, including their chemical-free nature and extraordinarily long lifetime. The long lifetime is related to the much higher Brownian motion velocity than buoyancy. The reason why ultrafine bubbles can endure under stable conditions is still unclear, even though their inside is highly pressured. They have several characteristics, such as pH-dependent surface charge and reduction in friction. They are also closely related to ultrasound. Ultrafine bubbles are generated and removed by selecting the ultrasonic frequency. Reaction and separation using ultrasonic cavitation and atomization, respectively, are enhanced by ultrafine bubbles. They can produce hollow nanoparticles, enhance adsorption on activated carbon, and clean solid surfaces. This review discusses the fundamental and ultrasonic characteristics of ultrafine bubbles and their application to particle-related technology: fine particle synthesis, adsorption, desorption, extraction, cleaning, and prevention of fouling.

Conceptualizing flexible papers using cellulose model surfaces and polymer particles.

Cellulose, as a naturally abundant and biocompatible material, is still gaining interest due to its high potential for functionalization. This makes cellulose a promising candidate for replacing plastics. Understanding how cellulose interacts with various additives is crucial for creating composite materials with diverse properties, as it is the case for plastics. In addition, the mechanical properties of the composite materials are assumed to be related to the mobility of the additives against the cellulose. Using a well-defined cellulose model surface (CMS), we aim to understand the adsorption and desorption of two polymeric particles (core-shell particles and microgels) to/from the cellulose surface. The nanomechanics of particles and CMS are quantified by indentation measurements with an atomic force microscope (AFM). AFM topography measurements quantified particle adsorption and desorption on the CMS, while peak force AFM measurements determined the force needed to move individual particles. Both particles and the CMS exhibited pH-dependent charge behavior, allowing a tunable interaction between them. Particle adsorption was irreversible and driven by electrostatic forces. In contrast, desorption and particle mobility forces are dominated by structural morphology. In addition, we found that an annealing procedure consisting of swelling/drying cycles significantly increased the adhesion strength of both particles. Using the data, we achieve a deeper understanding of the interaction of cellulose with polymeric particles, with the potential to advance the development of functional materials and contribute to various fields, including smart packaging, sensors, and biomedical applications.

Experimental Investigation of Lanthanum-Modified Reinforced Composite Material for Phosphorus Removal

Adsorption stands as an economically viable, efficient, recyclable, operationally straightforward, cost-effective, and low-sludge method extensively employed for phosphorus removal. In an effort to enhance the adsorption capabilities of the adsorbent, this study employs the rare-earth metal lanthanum in conjunction with the group’s previously researched high-efficiency composite industrial residue phosphorus removal materials (EPRC) for modification, thereby generating lanthanum-modified reinforced composite phosphorus removal materials (La-EPRC). Subsequently, the novel material undergoes static modification, followed by experimental investigations into static and dynamic adsorption for phosphorus removal. Static adsorption experiments reveal optimal phosphorus removal efficiency when the initial phosphorus solution concentration is 20 mgP/L, with a La-EPRC particle dosage of 3 g/250 mL and a temperature of 25 °C. The removal efficiency of phosphorus particles is above 90% within the pH range of 4 to 10. Common coexisting anions in water, including Cl−, SO42−, HCO3−, and CO32−, demonstrate minimal impact on the efficacy of phosphorus removal. La-EPRC demonstrates a robust adsorption stability in both water and hot water environments. In a 2.5 mol/L NaOH solution, effective desorption of La-EPRC particles is observed, facilitating material regeneration. The raw materials for La-EPRC are easily accessible and cost-effective, imparting significant potential for widespread applications.

Preparation of acid-responsive antibubbles from CaCO3-based Pickering emulsions

Hypothesis: Hydrophobized fumed silica particles were previously reported for producing antibubbles that are quite stable in neutral as well as in acidic media. To produce acid-responsive antibubbles (e.g., for gastric drug delivery), the silica nanoparticles must be replaced by suitable particles, e.g., calcium carbonate (CaCO3), which can degrade at low pH to release the encapsulated drug.Experiments: Two variants of CaCO3-stabilized antibubbles were prepared (by using CaCO3 particles pre-coated with stearic acid, or by using native CaCO3 particles in combination with sodium stearoyl lactylate) and drug release was compared with classic antibubbles produced with hydrophobized fumed silica particles.Findings: CaCO3 particles (pre-coated with stearic acid) can be used to produce stable antibubbles, which provided an entrapment efficiency of a model drug (methylene blue, MB) of around 85%. A burst release of MB (∼60%) from the antibubbles was observed at pH 2 (i.e., the pH of the stomach), which was further increased to 80% during the next 30 min. On the contrary, at neutral pH, about 70% of the drug remained encapsulated for at least 2 h. We further demonstrated that the acidic conditions led to the desorption of CaCO3 particles from the air–liquid interface resulting in the destabilization of the antibubbles and the release of drug-containing cores.

Wettability gradient-driven droplets with an applied external force.

On homogeneous substrates, droplets can slide due to external driving forces, such as gravity, whereas in the presence of wettability gradients, sliding occurs without external forces since this gradient gives rise to an internal driving force. Here, we study via molecular dynamics simulations the more complex behavior when droplets are driven under the combined influence of an external and internal driving force. For comparison, the limiting cases of a single driving force are studied as well. During a large part of the sliding process over the borderline of both substrates, separating both wettabilities, the velocity is nearly constant. When expressing it as the product of the effective mobility and the effective force, the effective mobility mainly depends on the mobility of the initial substrate, experienced by the receding contact line. This observation can be reconciled with the properties of the flow pattern, indicating that the desorption of particles at the receding contact line is the time-limiting step. The effective force is the sum of the external force and a renormalized internal force. This renormalization can be interpreted as stronger dissipation effects when driving occurs via wettability gradients.

Decoupling of Barium and Silicon at the Congo River‐Dominated Southeast Atlantic Margin: Insights From Combined Barium and Silicon Isotopes

AbstractThe correlation between concentrations of dissolved barium (dBa) and silicon (dSi) in the modern ocean supports the use of Ba as a paleoceanographic proxy. However, the mechanisms behind their linkage and the exact processes controlling oceanic Ba cycling remain enigmatic. To discern the extent to which this association arises from biogeochemical processes versus physical mixing, we examine the behavior of Ba and Si at the Congo River‐dominated Southeast Atlantic margin where active biological processes and large boundary inputs override the large‐scale ocean circulation. Here we present the first combined measurements of dissolved stable Ba (δ138Ba) and Si (δ30Si) isotopes as well as Ba and Si fluxes estimated based on 228Ra from the Congo River mouth to the northern Angola Basin. In the surface waters, river‐borne particle desorption or dissolution and shelf inputs lead to non‐conservative additions of both dBa and dSi to the Congo‐shelf‐zone, with the Ba flux increasing more strongly than that of Si across the shelf. In the epipelagic and mesopelagic layers, Ba and Si are decoupled likely due to different depths of in situ barite precipitation and biogenic silica production. In the deep waters of the northern Angola Basin, we observe large enrichment of dBa, likely originating from high benthic inputs from the Congo deep‐sea fan sediments. Our results reveal different mechanisms controlling the biogeochemical cycling of Ba and Si and highlight a strong margin influence on marine Ba cycling. Their close association across the global ocean must therefore mainly be a consequence of the large‐scale ocean circulation.

Pickering emulsions produced with kraft lignin colloids destabilized by in situ pH shift: Effect of emulsification energy input and stabilization mechanism

We introduce Kraft lignin colloids produced by destabilization of a kraft lignin solution by pH shift from 2 to 11. The system includes lignin particles and hydrocolloid aggregates in equilibrium (KLP), which are used to control the emulsifying energy and to stabilize oil-in-water emulsions under high energy at pH 11 and 7, yielding excellent stability (at least three months with no creaming). We investigate emulsify technology (ultrasonication and homogenization), energy input (high energy or low energy), particle desorption, drop size, and rheology on the stability of KLP-based Pickering emulsions according to the system’s pH. The ultrasonication leads to fine, stable and homogenous lignin emulsions without observing macroscopic creaming phenomenon, whereas homogenization only limits to alkaline condition. Regarding homogenization process, increasing the energy input helps to reduce the emulsion droplet size and consequently improves emulsion stability. In addition, the emulsion produced at acidic conditions always presented excellent stability, independent of the emulsify parameters. Considering the synergistic effects of emulsification protocol, surface activity, and particle interactions, the results indicate the possibility of extending the applications of kraft lignin as a Pickering stabilizer in neutral and alkaline conditions. It also creates a promising method to control the stability and emulsion microstructure in the industrial KLP based emulsion preparation process.

Tailoring the Asymmetric Structure of NH2‐UiO‐66 Metal‐Organic Frameworks for Light‐promoted Selective and Efficient Gold Extraction and Separation

AbstractDesigning adsorption materials with high adsorption capacities and selectivities is highly desirable for precious metal recovery. Desorption performance is also particularly crucial for subsequent precious metal recovery and adsorbent regeneration. Herein, a metal–organic framework (MOF) material (NH2‐UiO‐66) with an asymmetric electronic structure of the central zirconium oxygen cluster has an exceptional gold extraction capacity of 2.04 g g−1under light irradiation. The selectivity of NH2‐UiO‐66 for gold ions is up to 98.8 % in the presence of interfering ions. Interestingly, the gold ions adsorbed on the surface of NH2‐UiO‐66 spontaneously reduce in situ, undergo nucleation and growth and finally achieve the phase separation of high‐purity gold particles from NH2‐UiO‐66. The desorption and separation efficiency of gold particles from the adsorbent surface reaches 89 %. Theoretical calculations indicate that ‐NH2functions as a dual donor of electrons and protons, and the asymmetric structure of NH2‐UiO‐66 leads to energetically advantageous multinuclear gold capture and desorption. This adsorption material can greatly facilitate the recovery of gold from wastewater and can easily realize the recycling of the adsorbent.

Tailoring the Asymmetric Structure of NH2 -UiO-66 Metal-Organic Frameworks for Light-promoted Selective and Efficient Gold Extraction and Separation.

Designing adsorption materials with high adsorption capacities and selectivities is highly desirable for precious metal recovery. Desorption performance is also particularly crucial for subsequent precious metal recovery and adsorbent regeneration. Herein, a metal-organic framework (MOF) material (NH2 -UiO-66) with an asymmetric electronic structure of the central zirconium oxygen cluster has an exceptional gold extraction capacity of 2.04 g g-1 under light irradiation. The selectivity of NH2 -UiO-66 for gold ions is up to 98.8 % in the presence of interfering ions. Interestingly, the gold ions adsorbed on the surface of NH2 -UiO-66 spontaneously reduce in situ, undergo nucleation and growth and finally achieve the phase separation of high-purity gold particles from NH2 -UiO-66. The desorption and separation efficiency of gold particles from the adsorbent surface reaches 89 %. Theoretical calculations indicate that -NH2 functions as a dual donor of electrons and protons, and the asymmetric structure of NH2 -UiO-66 leads to energetically advantageous multinuclear gold capture and desorption. This adsorption material can greatly facilitate the recovery of gold from wastewater and can easily realize the recycling of the adsorbent.

Explosive desorption induced by radical–radical interaction in methane-doped Ar matrices

Delayed explosive desorption of particles from Ar matrices highly doped with CH4 stimulated by an electron irradiation was studied using emission spectroscopy methods. The recorded cathodoluminescence (CL) spectra of CH4-containig Ar matrices revealed following products of radiation-induced CH4 transformation: H, CH and C. Three series of experiments were performed with different irradiation and heating modes: (i) continuous irradiation at low temperature with accumulation of radiolysis products, (ii) heating of the pre-irradiated films with measurements of relaxation emissions, specifically thermally stimulated exoelectron emission (TSEE) and (iii) external heating of the pre-irradiated films under beam. These measurments of the, so called, nonstationary luminescenve (NsL) at the selected wavelenghs and nonstationary desorption (NsD) in combination with TSEE recorded provided an information on reactions of charged and neutral species of interest. Taking into account that the CH radical can be considered as a signature of the CH3 species [27] we obtained the information on a role of H atoms and CH3 radicals in stimulation of explosive delayed desorption of particles from Ar matrices doped with CH4. Two bursts of long-period self-oscillations together with short-period ones with a limited number of periods were observeed during stationary irradiation of all CH4-doped Ar matrices at low temperatures. Processes leading to the self-oscillations of particle yield are discussed.

Demulsification of Silica Stabilized Pickering Emulsions Using Surface Freezing Transition of CTAC Adsorbed Films at the Tetradecane-Water Interface.

The adsorbed film of cetyltrimethylammonium chloride (CTAC) at the tetradecane (C14) - water interface undergoes a first-order surface transition from two-dimensional liquid to solid states upon cooling. In this paper, we utilized this surface freezing transition to realize a spontaneous demulsification of Pickering emulsions stabilized by silica particles. In the temperature range above the surface freezing transition, the interfacial tension of silica laden oil-water interface was lower than CTAC adsorbed film, hence, stable Pickering emulsion was obtained by vortex mixing. However, the interfacial tension of CTAC adsorbed film decreased rapidly below the surface freezing temperature and became lower than the silica laden interface. The reversal of the interfacial tensions between silica laden and CTAC adsorbed films gave rise to Pickering emulsion demulsification by the desorption of silica particles from the oil-water interface. The exchange of silica particles and CTAC at the surface of emulsion droplets was also confirmed experimentally by using phase modulation ellipsometry at the oil-water interface.