Classification of regimes determining ultrasonic cavitation erosion in solid particle suspensions

Although the factors that influence ultrasonic cavitation erosion in solid particle suspensions have been extensively studied, the role that solid particles play in the cavitation process remains poorly understood. The ultrasonic cavitation erosion of AISI 1045 carbon steel was studied in the presence of monodisperse silica particles (10–100 μm, 0.5–20 vol%) suspended in transformer oil. Based on our results, we propose an overview of the possible influencing mechanisms of particle addition for specific particle sizes and concentrations. Four major regimes, namely a viscosity-enhancing regime (V), a particle-impinging regime (I), a particle-shielding regime (S), and a nuclei-adding regime (A) are identified, and their dependence on suspended particle characteristics is analyzed. The VISA regimes, in essence, reflect the viscous and inertial effects of suspended particles, and the way in which particle–particle interactions and heterogeneous nucleation affect erosion. This regime-based framework provides a better understanding of the dominant factors controlling the erosive wear caused by cavitation in the presence of solid particles, and provides a guide for erosion prediction and prevention.     

Interaction force between a bubble and a solid particle in a sound field

The time-averaged interaction force exerted by a sound field between a gas bubble and a solid spherical particle is examined. An approach is developed allowing the force to be calculated for small separations between the bubble and the particle. The results obtained are compared with the existing asymptotic equation derived for large separations. It is shown that when the bubble and the particle are closely spaced, both the magnitude and the sign of the force are different from those predicted by the asymptotic equation, resulting in new interesting effects.     

The effect of heterogeneous solvent systems on sonochemical reactions: accelerated degradation of alkyl thiols in emulsion

Sonochemical reactions of alkyl and aryl thiols in water–organic mixed solvent systems were kinetically investigated. The reaction in the liquid–liquid interface apparently depends on the polarities, surface activities, vapor pressures and hydrophobicities of organic solvents and thiols. Interestingly, the rate jump in sonochemical disappearance of alkyl thiols was observed under emulsified conditions.     

The pH-dependent reactions in the sonochemical synthesis of luminescent fluorides: The quest for the formation of KY3F10 crystal phases

In this study Eu³⁺-doped yttrium fluorides were designed by ultrasound-assisted processes at different pH values (4.0–9.0). This novel strategy has enabled to obtain materials with intriguing morphologies and modulated crystal structures: α-KY₃F₁₀, δ–KY₃F₁₀·xH₂O, and Y(OH)_3–xF_x. To date, the literature has primarily focused only on the α-phase of KY₃F₁₀. Yet, explaining the formation of the mostly uncharted δ-phase of KY₃F₁₀ remains a challenge. Thus, this paper offers the key to synthesizing both the α and the δ-phases of KY₃F₁₀ and also reports the first ultrasound-assisted process for the preparation of yttrium hydroxyfluorides. It is also unraveled the connection between the different pH-dependent reactions and the formation mechanisms of the compounds. In addition to this, the unique features of the Eu³⁺ ion have allowed to conduct a thorough study of the different materials and have endowed the compounds with photoluminescent properties. The results underscore a highly tunable optical response, with a wide gamut of color emissions (from orangish to red hues), lifetimes (from 7.9 ms to 1.1 ms) and quantum efficiencies (98–28%). The study unveils the importance of sonochemistry in obtaining luminescent fluorides with controlled crystal structures that can open up new avenues in the synthesis and design of inorganic materials.     

Effect of steam on the single particle ignition of solid fuels in a drop tube furnace under air and simulated oxy-fuel conditions

This article investigates the effect of steam on the ignition of single particles of solid fuels in a drop tube furnace under air and simulated oxy-fuel conditions. Three solid fuels, all in the size range 125–150 µm, were used in this study; specifically, a low rank sub-bituminous Colombian coal, a low-rank/high-ash sub-bituminous Brazilian coal and a charcoal residue from black acacia. For each solid fuel, particles were burned at a constant drop tube furnace wall temperature of 1475?K, in six different mixtures of O₂/N₂/CO₂/H₂O, which allowed simulating dry and wet conventional and oxy-fuel combustion conditions. A high-speed camera was used to record the ignition process and the collected images were treated to characterize the ignition mode (either gas-phase or surface mode) and to calculate the ignition delay times. The Colombian coal particles ignite predominately in the gas-phase for all test conditions, but under simulated oxy-fuel conditions there is a decrease in the occurrence of this ignition mode; the charcoal particles experience surface ignition regardless of the test condition; and the Brazilian coal particles ignite predominately in the gas-phase when combustion occurs in mixtures of O₂/N₂/H₂O, but under simulated oxy-fuel conditions the ignition occurs predominantly on the surface. The ignition delay times for particles that ignited in the gas-phase are smaller than those that ignited on the surface, and generally the simulated oxy-fuel conditions retard the onset of both gas-phase and surface ignition. The addition of steam decreases the gas-phase and surface ignition delay times of the particles of both coals under simulated oxy-fuel conditions, but has a small impact on the gas-phase ignition delay times when the combustion occurs in mixtures of O₂/N₂/H₂O. The steam gasification reaction is likely to be responsible for the steam effect on the ignition delay times through the production of highly flammable species that promote the onset of ignition.     

Electron paramagnetic resonance of sonicated powder suspensions in organic solvents

The chemical effects of the acoustic cavitation generated by ultrasound translates into the production of highly reactive radicals. Acoustic cavitation is widely explored in aqueous solutions but it remains poorly studied in organic liquids and in particular in liquid/solid media. However, several heterogeneous catalysis reactions take place in organic solvents.Thus, we sonicated trimethylene glycol and propylene glycol in the presence of silica particles (SiO₂) of different sizes (5–15 nm, 0.2–0.3 µm, 12–26 µm) and amounts (0.5 wt% and 3 wt%) at an ultrasound frequency of 20 kHz to quantify the radicals generated. The spin trap 5,5-dimethyl-1-pyrrolin–N-oxide (DMPO) was used to trap the generated radicals for study by electron paramagnetic resonance (EPR) spectroscopy. We identified the trapped radical as the hydroxyalkyl radical adduct of DMPO, and we quantified it using stable radical 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) as a quantitation standard. The concentration of DMPO spin adducts in solutions containing silica size 12–26 µm was higher than the solution without particles. The presence of these particles increased the concentration of the acoustically generated radicals by a factor of 1.5 (29 µM for 0.5 wt% of SiO₂ size 12–26 µm vs 19 µM for 0 wt%, after 60 min of sonication). Ultrasound produced fewest radicals in solutions with the smallest particles; the concentration of radical adducts was highest for SiO₂ particle size 12–26 µm at 0.5 wt% loading, reaching 29 µM after 60 min sonication. Ultrasound power of 50.6 W produced more radicals than 24.7 W (23 µM and 18 µM, respectively, at 30 min sonication). Increased temperature during sonication generated more radical adducts in the medium (26 µM at 75 °C and 18 µM at 61 °C after 30 min sonication). Acoustic cavitation, in the presence of silica, increased the production of radical species in the studied organic medium.     

Study of pre-scission particle emissions and fission probability of the l78W produced in fusion reactions

A dynamical model based on one-dimensional Langevin equations was used to calculate the average pre-fission multiplicities of neutrons, light charged particles, and the fission probability for compound nucleus 17Sw produced in fusion reactions. The pre-seission multiplicities of particles and fission probability are calculated and compared with the experimental data over a wide range of excitation energy. A modified wall and window dissipation with a reduction coefficient, ks, has been used in the Langevin equations for reproducing experimental data. It was shown that the results of the calculations are in good agreement with the experimental data by using values of ks in the range 0.24〈 ks 〈0.47.     

Direct observations of single particle fragmentation in the early stages of combustion under dry and wet conventional and oxy-fuel conditions

This article investigates the single particle fragmentation of three solid fuels in the early stages of combustion under dry and wet conventional and oxy-fuel conditions. The three solid fuels studied were a low rank sub-bituminous Colombian coal, a low-rank/high-ash sub-bituminous Brazilian coal, and a charcoal residue from black acacia. Particles, with size in the range 125–150 µm, were burned in a drop tube furnace with a constant wall temperature of 1475?K, under six different mixtures of O₂/N₂/CO₂/H₂O, which allowed simulating dry and wet conventional and oxy-fuel combustion conditions. A high-speed camera was used to record the fragmentation process during the early stages of combustion and the collected images were treated to characterize the fragmentation mode, probability and time. The observed fragmentation modes are characterized by the occurrence of exfoliation, radial fragmentation or a combination of both. The results disclose that the fragmentation mode is strongly affected by the fuel type, but less affected by the atmosphere; the fragmentation probability is strongly affected by both the fuel type and the atmosphere; and, finally, fragmentation in air occurs significantly dispersed after ignition, but it tends to cluster closer to the ignition under simulated oxy-fuel conditions.     

Study of pre-scission particle emissions and fission probability of the ~(178)W produced in fusion reactions

A dynamical model based on one-dimensional Langevin equations was used to calculate the average pre-fission multiplicities of neutrons, light charged particles, and the fission probability for compound nucleus178 W produced in fusion reactions. The pre-scission multiplicities of particles and fission probability are calculated and compared with the experimental data over a wide range of excitation energy. A modified wall and window dissipation with a reduction coefficient, ks, has been used in the Langevin equations for reproducing experimental data. It was shown that the results of the calculations are in good agreement with the experimental data by using values of ks in the range 0.24 ks 0.47.