Review on the impacts of external pressure on sonochemistry.

The impact of hydrostatic pressure, commonly known as ambient or external pressure, on the phenomenon of sonochemistry and/or sonoluminescence has been extensively investigated through a multitude of experimental and computational studies, all of which have emphasized the crucial role played by this particular parameter. Numerous previous studies have successfully demonstrated the existence of an optimal static pressure for the occurrence of sonoluminescence and multi-bubble or single-bubble sonochemistry. However, despite these findings, a universally accepted value for this critical pressure has not yet been established. In addition, it has been found that the cavitation effect is completely inhibited when the static pressure is either too high or too low. This comprehensive review aims to delve into the primary experimental results and elucidate their significance in relation to hydrostatic pressure. We will then conduct an analysis of numerical calculations, focusing specifically on the influence of external pressure on single bubble sonochemistry. By delving into these calculations, we will be able to gain a deeper understanding of the experimental results and effectively interpret their implications.

Sonochemistry dosimetries in seawater.

Due to the complex physical and chemical interactions taking place in the sonicated medium, various methods have been proposed in the literature for a better understanding of the sonochemical system. In the present paper, the performance of calorimetry, iodometry, Fricke, 4-nitrophenol, H2O2, and ascorbic acid dosimetry techniques have been evaluated over the electric power range from 20 to 80 W (f = 300 kHz). These methods have been analyzed for distilled and seawater in light of the literature findings. It has been found that the lowest temperatures and calorimetric energies were obtained for seawater in comparison to distilled water. However, the discrepancy between both mediums disappears with the increase in the electric power up to 80 W. Compared to the calorimetry results, a similar trend was obtained for the KI dosimetry, where the discrepancy between both solutions (seawater and distilled water) increased with the reduction in the electric power down to 20 W. In contrast, over the whole range of the electric power (20-80 W), the H2O2 dosimetry was drastically influenced by the salt composition of seawater, where, I3- formation was clearly reduced in comparison to the case of the distilled water. On the other hand, a fluctuated behavior was observed for the Fricke and 4-nitrophenol dosimetry methods, especially at the low electric powers (20 and 40 W). It has been found that dosimetry techniques based on ascorbic acid or potassium iodide are the best means for accurate quantification of the sonochemical activity in the irradiated liquid. As a result, it has been concluded, in terms of the dosimetry process's performance, that the dosimetry methods are in the following order: Ascorbic acid ≈ KI > Fricke > 4-nitrophenol > H2O2.

Application of the general rate law model to the sonolytic degradation of nonvolatile organic pollutants in aqueous media.

The pseudo-first and pseudo-second order equations have been the most commonly used models to characterize the sonolytic disappearance kinetics of nonvolatile pollutants in aqueous media. In this work, the general rate law model, i.e., pseudo-nth order kinetics equation, was applied for the first time to the sono-decomposition of different nonvolatile organic pollutants, naphthol blue black (NBB), furosemide (FSM), 4-isopropylphenol (4-IPP), and rhodamine B (RhB), in water. It was shown that the general rate law for a chemical reaction would apply to the kinetics of sonochemical decomposition. It is not feasible to set the order of ultrasonic pollutant degradation kinetics to pseudo-first or pseudo-second, as is typically used in numerous studies. The sonochemical oxidation reaction has a fractional order, the order is often non-integer, which frequently indicates a complex sonolytic decomposition reaction mechanism. The degradation mechanism of NBB and RhB does not change with the initial substrate concentration. They are ultrasonically degraded by hydroxyl radicals both in the bulk liquid solution and at the liquid/bubble interfacial layer. The destruction mechanism of FSM and 4-IPP changes as the initial contaminant concentration changes. At low initial substrate concentrations, these pollutants are oxidized mainly by reaction with hydroxyl radicals in the bulk liquid solution and at the interfacial shell of the cavitation bubbles. At high initial substrate concentrations, FSM and 4-IPP are degraded by thermal destruction in the liquid/bubble interfacial layer and by •OH radicals both in the bulk liquid solution and at the liquid/bubble interfacial layer. Additionally, the pseudo-nth order model predicts very well the sonolytic degradation at various sonication frequencies and intensities. The general rate law expression should be used to assess the real kinetics order of the sonolytic destruction process without any predetermined assumptions or constraints.

Sonochemical reactor characterization in the presence of cylindrical and conical reflectors.

Ultrasonic systems must be able to produce an acoustic field with the highest possible energy concentration in sonochemical reactors to accomplish maximum efficacy in the sonolytic degradation of water contaminants. In the present study, the impact of cylindrical and conical stainless-steel reflectors placed on the liquid surface on the sonochemical oxidation activity of ultrasonication reactors was investigated. The amount of effective acoustic power transferred to the ultrasonicated medium without and with reflectors was measured by calorimetric characterization of the sono-reactors at diverse ultrasonication frequencies in the interval of 300-800 kHz and different electrical powers in the range of 40-120 W. Iodide dosimetry without and with reflectors at diverse ultrasonication conditions (300-800 kHz and 40-120 W) and various aqueous solution volumes in the range of 300-500 mL was used to assess the sonochemical oxidation activity, i.e., the generation of oxidative species (mainly hydroxyl radicals). Sonochemiluminescence (SCL) imaging was used to study the active acoustic cavitation bubbles distribution in the sono-reactors without and with reflectors. Significant impacts of the position and shape of the reflectors on the active acoustic cavitation bubble distribution and the sonochemical oxidation activity were observed due to remarkable modifications of the ultrasonic field by directing and focusing of the ultrasonic waves. A significant augmentation in the triiodide formation rate was obtained in the presence of the conical reflector, especially at 630 kHz and 120 W (60.5% improvement), while iodide oxidation was quenched in the presence of the cylindrical reflector at all ultrasonication frequencies and powers. The SCL images show a noteworthy modification in the ultrasonic field and the acoustic cavitation bubble population when reflectors were used. The sonochemical oxidation activity was improved by the conical reflector when placed in the Fresnel zone (near field region).

General analytical solution expressions for analyzing Langmuir-type kinetics of sonochemical degradation of nonvolatile organic contaminants in water.

Detailed kinetic studies of the ultrasonic decomposition of contaminants in water are scarce. Most of the work has used a pseudo-first order kinetics law, which is unrealistic. The model based on a Langmuir-type mechanism has been shown to fit the sonolytic decomposition data well, especially by using the non-linear technique. To avoid unrealistic assumptions, general analytical solutions to a time-dependent non-linear Langmuir-type equation may be the appropriate method. In this work, the sonolytic oxidation of organic contaminants, i.e., naphthol blue black and furosemide, in water was analyzed using two general analytical solution expressions of the Langmuir-type kinetics model, which describe the pollutant concentration in water. The validity of the two general analytical solution expressions was tested under a diversity of operating conditions, such as initial substrate concentration and varying ultrasonication frequency and intensity. As the initial substrate concentration increased, the sonolytic oxidation kinetics decreased, while the initial ultrasonic decomposition rate increased and then plateaued. Consequently, a heterogeneous kinetics equation based on a Langmuir-type mechanism can be used to simulate the sono-decomposition process. The decomposition yield increased with increasing sonication intensity and decreasing frequency. The two analytical solution expressions seem to be in excellent agreement with the experimental results of the sonochemical decomposition of the nonvolatile organic contaminants tested for the different operating conditions examined. These expressions provide a valuable tool for the analysis and simulation of advanced sonochemical oxidation processes under various experimental conditions.

Sonochemical formation of peroxynitrite in water: Impact of ultrasonic frequency and power.

There is a lack of literature on peroxynitrite formation due to sonolysis of aerated water. In this work, the impact of sonication parameters, frequency and power, on ultrasonic peroxynitrite production in aerated alkaline water was investigated. Peroxynitrite formation was clearly established with undeniable evidence at all the tested frequencies in the range of 516-1140 kHz with a typical G-value (energy-specific yield) of 0.777 × 10-10, 0.627 × 10-10, 0.425 × 10-10 and 0.194 × 10-10 mol/J at 516, 558, 860 and 1140 kHz, respectively. The ultrasonication frequency has a direct impact on the sonochemical peroxynitrite production. Increasing the ultrasonication frequency in the interval 321-1140 kHz reduces peroxynitrite formation. The most practical sonochemistry dosimetries, including hydrogen peroxide production, triiodide dosimetry, Fricke dosimetry, and 4-nitrocatechol formation, were compared with the sonochemical efficiency of the reactors used to produce peroxynitrite. The G-value, energy specific yield, for the tested dosimetries was higher than that for peroxynitrite formation, regardless of frequency. For all chemical dosimetries investigated, the same trend of frequency dependence was found as for peroxynitrite generation. The influence of ultrasonication power on peroxynitrite formation by sonication at diverse frequencies in the interval 585-1140 kHz was studied. No peroxynitrite was formed at lower acoustic power levels, regardless of frequency. As the frequency increases, more power is required for peroxynitrite formation. The production of peroxynitrite increased as the acoustic power increased, despite the frequency of ultrasonic waves. Ultrasonic power is a key factor in the production of peroxynitrite by sonolysis. Since peroxynitrite is uniformly distributed in the bulk solution, peroxynitrite-sensitive solutes can be transformed both in the bulk of the solution and in the surfacial region (shell) of the cavitation bubble. The formation of peroxynitrite should be taken into account in sonochemistry, especially at higher pH values. Ultrasonic peroxynitrite formation in alkaline solution (pH 12) can be considered as a kind of chemical dosimetry in sonochemistry.

Phase Change Material (PCM)-based thermal storage system for managing the sonochemical reactor heat: Thermodynamic analysis of the liquid height impact.

As an alternative to a water-based cooling system for a sonoreactor, the present work presents for the first time the use of a phase change material for the management and storage of the dissipated heat within the sonicated water. The performance of the PCM is analyzed as a function of liquid height (LH = 5.1, 10.2, 15.3, and 20.4 cm) at a frequency of 300 kHz and two electric powers (PE = 20 and 60 W). The effective powers dissipated in the irradiated water were determined by the calorimetric technique. A computational fluid dynamics (CFD) model (implemented in ANSYS Fluent® software), was used for the analysis of the combined system (sonoreactor + PCM-thermal unit) at different operating conditions (liquid height and electric power). By analyzing the different outputs (variation of temperature, velocity, enthalpy, liquid fraction of PCM) of the used CFD model, more clarifications are provided about the behaviour of the combined system (sonoreactor + PCM-thermal unit) as function of the liquid height (5.1-20.4 cm) and electric power (20 and 60 W). In terms of temperature, velocity, enthalpy and liquid fraction of the PCM, promising results were obtained in spite of the low thermal conductivity of the employed PCM. The best performance of the combined system (sonoreactor and thermal unit) was obtained at the liquid height of 15.3 cm (corresponding to a water volume of 300 mL) with a similar behaviour (evolution of temperature, velocity, enthalpy, and liquid fraction of the PCM) at both electric powers (i.e., 20 and 60 W) with an intensified response at the PE = 60 W.

Biosorption of Triphenyl Methane Dyes (Malachite Green and Crystal Violet) from Aqueous Media by Alfa (Stipa tenacissima L.) Leaf Powder.

This study includes the characterization and exploitation of an abundant agricultural waste in Algeria, Alfa (Stipa tenacissima L.) leaf powder (ALP) as a biosorbent for the removal of hazardous triphenylmethane dyes, malachite green (basic green 4) and crystal violet (basic violet 3), from aqueous media under various operating conditions in batch mode. The effect of experimental parameters such as initial dye concentration (10-40 mg/L), contact time (0-300 min), biosorbent dose (2.5-5.5 g/L), initial pH (2-8), temperature (298-328 K), and ionic strength on dye sorption was investigated. The results of both dyes show that the increase in initial concentration, contact time, temperature, and initial pH of solution leads to an increase in biosorbed quantity, unlike the effect of ionic strength. The biosorption kinetics for triphenylmethane dyes on ALP was analyzed by pseudo-first-order, pseudo-second-order, Elovich, and intraparticle diffusion models proposed by the Weber-Morris equation. Equilibrium sorption data were analyzed by six isotherms, namely the Langmuir, Freundlich, Harkins-Jura, Flory-Huggins, Elovich, and Kiselev isotherms. The thermodynamic parameters were evaluated for both dyes. The thermodynamic results suggest that both dyes' biosorption is a typical physical process, spontaneous and endothermic in nature.

The impact of methanol mass transport on its conversion for the production of hydrogen and oxygenated reactive species in sono-irradiated aqueous solution.

This study aims principally to assess numerically the impact of methanol mass transport (i.e., evaporation/condensation across the acoustic bubble wall) on the thermodynamics and chemical effects (methanol conversion, hydrogen and oxygenated reactive species production) of acoustic cavitation in sono-irradiated aqueous solution. This effect was revealed at various ultrasound frequencies (from 213 to 1000 kHz) and acoustic intensities (1 and 2 W/cm2) over a range of methanol concentrations (from 0 to 100%, v/v). It was found that the impact of methanol concentration on the expansion and compression ratios, bubble temperature, CH3OH conversion and the molar productions inside the bubble is frequency dependent (either with or without consideration of methanol mass transport), where this effect is more pronounced when the ultrasound frequency is decreased. Alternatively, the decrease in acoustic intensity decreases clearly the effect of methanol mass transport on the bubble sono-activity. When methanol mass transfer is eliminated, the decrease of the bubble temperature, CH3OH conversion and the molar yield of the bubble with the rise of methanol concentration was found to be more amortized as the wave frequency is reduced from 1 MHz to 213 kHz, compared to the case when the mass transport of methanol is taken into account. Our findings indicate clearly the importance of incorporating the evaporation and condensation mechanisms of methanol throughout the numerical simulations of a single bubble dynamics and chemical activity.

Sonochemical advanced oxidation process for the degradation of furosemide in water: Effects of sonication's conditions and scavengers.

The intensive consumption of pharmaceuticals and drugs in the last decades has led to their increased concentrations in wastewaters from industrial sources. The present paper deals, for the first time, with the sonochemical degradation and mineralization of furosemide (FSM) in water. FSM is a potent loop diuretic used to treat fluid build-up due to heart failure, liver scarring, or kidney disease. The influence of several operating parameters such as acoustic intensity, ultrasonic frequency, initial FSM concentration, solution's pH, nature of the dissolved gas (Ar, air and N2) and radical scavengers (2-propanol and tert-butanol) on the oxidation of FSM was assessed. The obtained results showed that the degradation rate of the drug increased significantly with the increase of the acoustic intensity in the range of 0.83 to 4.3 W cm-2 and decreased with the augmentation of the frequency in the range of 585-1140 kHz. It was also found that the initial rate of the sonolytic degradation of FSM increased with the increase of its initial concentration (2, 5, 10, 15 and 20 mg/L). The most significant degradation was achieved in acidic conditions at pH 2, while in terms of saturating gas, the rate of FSM degradation decreased in the order of Ar > air > N2. The FSM degradation experiments with radical scavengers showed that the diuretic molecule degraded mainly at the interfacial region of the bubble by hydroxyl radical attack. Additionally, in terms of acoustic conditions, the sono-degradation of 30.24 µmol L-1 of FSM solution demonstrate an optimal performance at 585 kHz and 4.3 W/cm2, the results indicated that even if the ultrasonic action eliminated the total concentration of FSM within 60 min, a low degree of mineralization was obtained due to the by-products formed during the sono-oxidation process. The ultrasonic process transforms FSM into biodegradable and environmentally friendly organic by-products that could be treated in a subsequent biological treatment. Besides, the efficiency of the sonolytic degradation of FSM in real environmental matrices such as natural mineral water and seawater was demonstrated. Consequently, the sonochemical advanced oxidation process represent a very interesting technique for the treatment of water contaminated with FSM.

Bibliometric analysis and literature review of ultrasound-assisted degradation of organic pollutants.

Ultrasound as a clean, efficient, and cheap technique gains special attention in wastewater treatment. Ultrasound alone or coupled with hybrid processes have been widely studied for the treatment of pollutants in wastewater. Thus, it is essential to conduct a review about the research development and trends on this emerging technique. This work presents a bibliometric analysis of the topic associated with multiple tools such as Bibliometrix package, CiteSpace, and VOSviewer. The literature sources from 2000 to 2021 were collected from Web of Science database, and the data of 1781 documents were selected for bibliometric analysis in respect to publication trends, subject categories, journals, authors, institutions, as well as countries. Detailed analysis of keywords in respect to co-occurrence network, keyword clusters, and citation bursts was conducted to reveal the research hotspot and future directions. The development of the topic can be divided into three stages, and the rapid development begins from 2014. The leading subject category is Chemistry Multidisciplinary, followed by Environmental Sciences, Engineering Chemical, Engineering Environmental, Chemistry Physical, and Acoustics, and there exists difference in the publications of different categories. Ultrasonics Sonochemistry is the most productive journal (14.75 %). China is the leading country (30.26 %), followed by Iran (15.67 %) and India (12.35 %). The top 3 authors are Parag Gogate, Oualid Hamdaoui, and Masoud Salavati-Niasari. There exists close cooperation between countries and researchers. Analysis of highly cited papers and keywords gives a better understanding of the topic. Ultrasound can be employed to assist various processes such as Fenton-like process, electrochemical process, and photocatalysis for degradation of emerging organic pollutants for wastewater treatment. Research topics in this field evolve from typical studies on ultrasonic assisted degradation to latest studies on hybrid processes including photocatalysis for pollutants degradation. Additionally, ultrasound-assisted synthesis of nanocomposite photocatalysts receives increasing attention. The potential research directions include sonochemistry in pollutant removal, hydrodynamic cavitation, ultrasound-assisted Fenton or persulfate processes, electrochemical oxidation, and photocatalytic process.

Estimation of the number density of active cavitation bubbles in a sono-irradiated aqueous solution using a thermodynamic approach.

An alternative semi-empirical technique is developed to determine the number density of active cavitation bubbles (N) formed in sonicated solutions. This was achieved by relating the acoustic power supplied to the solution (i.e., determined experimentally) to the released heat by a single bubble. The energy dissipation via heat exchange is obtained by an advanced cavitation model accounting for the liquid compressibility and viscosity, the non-equilibrium condensation/evaporation of water vapor, and heat conduction across the bubble wall and heats of chemical reactions resulting within the bubble at the collapse. A good concordance was observed between our results and those found in the literature. It was found that the number of active bubbles increased proportionally with a rise in ultrasound frequency. Additionally, the increase of acoustic intensity increases the number of active bubbles, whatever the sonicated solution's volume. On the other hand, it was observed that the rise of the irradiated solution volume causes the number of active bubbles to be reduced even when the acoustic power is increased. A decrease in acoustic energy accelerates this negative impact.

Ultrasound/chlorine sono-hybrid-advanced oxidation process: Impact of dissolved organic matter and mineral constituents.

In this work, after exploring the first report on the synergism of combining ultrasound (US: 600 kHz) and chlorine toward the degradation of Allura Red AC (ARAC) textile dye, as a contaminant model, the impact of various mineral water constituents (Cl-, SO42-, NO3-, HCO3- and NO2-) and natural organic matter, i.e., humic acid (HA), on the performance of the US/chlorine sono-hybrid process was assessed for the first time. Additionally, the process effectiveness was evaluated in a real natural mineral water (NMW) of a known composition. Firstly, it was found that the combination of ultrasound and chlorine (0.25 mM) at pH 5.5 in cylindrical standing wave ultrasonic reactor (f = 600 kHz and Pe = 120 W, equivalent to PA âˆ¼ 2.3 atm) enhanced in a drastic manner the degradation rate of ARAC; the removal rate being 320% much higher than the arithmetic sum of the two separated processes. The source of the synergistic effect was attributed to the effective implication of reactive chlorine species (RCS: Cl, ClO and Cl2-) in the degradation process. Radical probe technique using nitrobenzene (NB) as a specific quencher of the acoustically generated hydroxyl radical confirmed the dominant implication of RCS in the overall degradation rate of ARAC by US/chlorine system. Overall, the presence of humic acid and mineral anions decreased the efficiency of the sono-hybrid process; however, the inhibition degrees depend on the type and the concentration of the selected additives. The reaction of these additives with the generated RCS is presumably the reason for the finding results. The inhibiting effect of Cl-, SO42-, NO3- and NO2- was more pronounced in US/chlorine process as compared to US alone, whereas the inverse scenario was remarked for the effect of HA. These outcomes were associated to the difference in the reactivity of HA and mineral anions toward RCS and OH oxidizing species, in addition to the more selective character of RCS than hydroxyl radical. The displacement of the reaction zone with increasing the additive concentration may also be another influencing factor that favors competition reactions, which subsequently reduce the available reactive species in the reacting medium. The NMW exerted reductions of 43% and 10% in the process efficiency at pH 5.5 and 8, respectively, thereby confirming the RCS-quenching mechanism by the water matrix constituents. Hence, this work provided a precise understanding of the overall mechanism of chlorine activation by ultrasound to promote organic compounds degradation in water.

The multiple role of inorganic and organic additives in the degradation of reactive green 12 by UV/chlorine advanced oxidation process.

The impact of various mineral anions, diverse organic substrates and different environmental matrices on the removal of C.I. reactive green 12 (RG12), a refractory textile dye, by UV/chlorine emerging advanced oxidation process (AOP) was performed. The co-exposure of RG12 (20 mg L-1) to UV and chlorine (0.5 mM) at pH 5 produced a strong synergism on the degradation rate. Radical probe technique showed that ●OH and Cl2●- were the main source of the synergistic effect. Bromide, bicarbonate and chloride at small dosage, i.e. 1 mM, enhanced the rate of RG12 degradation, but higher concentrations of these anions quenched the degradation process. Sulphate anions did not alter the degradation rate of the dye, but nitrite quenched it at ∼ 90%. The inhibiting effect of nitrate appeared only at advanced reaction time (>1 min).On the other hand, natural organic matter (NOM) reduced effectively the degradation rate. Besides, SDS surfactant at only 1 µM accelerated the degradation efficiency by ∼12%. However, Tween 80 has shown an insignificant effect, whereas reductions of 10% and 30% were recorded by Triton X100 and Tween 20, respectively. The RG12-degradation rate was not affected in the mineral water, but it was drastically improved in seawater. Conversely, a huge drop in the RG12-degradation efficiency was obtained in the wastewater effluent. UV/chlorine process is highly viable for degrading pollutant in matrices free of NOM. However, the process losses its potential application in matrices riche of NOM.

An alternative technique for determining the number density of acoustic cavitation bubbles in sonochemical reactors.

The present paper introduces a novel semi-empirical technique for the determination of active bubbles' number in sonicated solutions. This method links the chemistry of a single bubble to that taking place over the whole sonochemical reactor (solution). The probe compound is CCl4, where its eliminated amount within a single bubble (though pyrolysis) is determined via a cavitation model which takes into account the non-equilibrium condensation/evaporation of water vapor and heat exchange across the bubble wall, reactions heats and liquid compressibility and viscosity, all along the bubble oscillation under the temporal perturbation of the ultrasonic wave. The CCl4 degradation data in aqueous solution (available in literature) are used to determine the number density through dividing the degradation yield of CCl4 to that predicted by a single bubble model (at the same experimental condition of the aqueous data). The impact of ultrasonic frequency on the number density of bubbles is shown and compared with data from the literature, where a high level of consistency is found.

Galvano-Fenton Engineering Solution with Spontaneous Catalyst's Generation from Waste: Experimental Efficiency, Parametric Analysis and Modeling Interpretation Applied to a Clean Technology for Dyes Degradation in Water.

In this paper, the degradation of the diazo dye naphthol blue black (NBB) using the Galvano-Fenton process is studied experimentally and numerically. The simulations are carried out based on the anodic, cathodic, and 34 elementary reactions evolving in the electrolyte, in addition to the oxidative attack of NBB by HO• at a constant rate of 3.35×107 mol-1·m3·s-1 during the initiation stage of the chain reactions. The selection of the operating conditions including the pH of the electrolyte, the stirring speed, and the electrodes disposition is performed by assessing the kinetics of NBB degradation; these parameters are set to 3, 350 rpm and a parallel disposition with a 3 cm inter-electrode distance, respectively. The kinetics of Fe(III) in the electrolyte were monitored using the principles of Fricke dosimetry and simulated numerically. The model showed more than a 96% correlation with the experimental results in both the blank test and the presence of the dye. The effects of H2O2 and NBB concentrations on the degradation of the dye were examined jointly with the evolution of the simulated H2O2, Fe2+, and HO• concentrations in the electrolyte. The model demonstrated a good correlation with the experimental results in terms of the initial degradation rates, with correlation coefficients exceeding 98%.

A Novel Energy-from-Waste Approach for Electrical Energy Production by Galvano-Fenton Process.

A novel approach allowing the production of electrical energy by an advanced oxidation process is proposed to eliminate organic micropollutants (MPs) in wastewaters. This approach is based on associating the Galvano-Fenton process to the generation of electrical power. In the previous studies describing the Galvano-Fenton (GF) process, iron was directly coupled to a metal of more positive potential to ensure degradation of organic pollutants without any possibility of producing electrical energy. In this new approach, the Galvano-Fenton process is constructed as an electrochemical cell with an external circuit allowing recovering electrons exchanged during the process. In this study, Malachite Green (MG) dye was used as a model of organic pollutant. Simultaneous MG degradation and electrical energy production with the GF method were investigated in batch process. The investigation of various design parameters emphasis that utilization of copper as a low-cost cathode material in the galvanic couple, provides the best treatment and electrical production performances. Moreover, these performances are improved by increasing the surface area of the cathode. The present work reveals that the GF process has a potential to provide an electrical power density of about 200 W m-2. These interesting performances indicate that this novel Energy-from-Waste strategy of the GF process could serve as an ecological solution for wastewater treatment.

Insight into the impact of excluding mass transport, heat exchange and chemical reactions heat on the sonochemical bubble yield: Bubble size-dependency.

Numerical simulations have been performed on a range of ambient bubble radii, in order to reveal the effect of mass transport, heat exchange and chemical reactions heat on the chemical bubble yield of single acoustic bubble. The results of each of these energy mechanisms were compared to the normal model in which all these processes (mass transport, thermal conduction, and reactions heat) are taken into account. This theoretical work was carried out for various frequencies (f: 200, 355, 515 and 1000 kHz) and different acoustic amplitudes (PA: 1.5, 2 and 3 atm). The effect of thermal conduction was found to be of a great importance within the bubble internal energy balance, where the higher rates of production (for all acoustic amplitudes and wave frequencies) are observed for this model (without heat exchange). Similarly, the ignorance of the chemical reactions heat (model without reactions heat) shows the weight of this process into the bubble internal energy, where the yield of the main species (OH, H, O and H2) for this model was accelerated notably compared to the complete model for the acoustic amplitudes greater than 1.5 atm (for f = 500 kHz). However, the lowest production rates were registered for the model without mass transport compared to the normal model, for the acoustic amplitudes greater than 1.5 atm (f = 500 kHz). This is observed even when the temperature inside bubble for this model is greater than those retrieved for the other models. On the other hand, it has been shown that, at the acoustic amplitude of 1.5 atm, the maximal production rates of the main species (OH, H, O and H2) for all the adopted models appear at the same optimum ambient-bubble size (R0 ~ 3, 2.5 and 2 µm for, respectively, 355, 500 and 1000 kHz). For PA = 2 and 3 atm (f = 500 kHz), the range of the maximal yield of OH radicals is observed at the range of R0 where the production of OH, O and H2 is the lowest, which corresponds to the bubble temperature at around 5500 K. The maximal production rate of H, O and H2 is shifted toward the range of ambient bubble radii corresponding to the bubble temperatures greater than 5500 K. The ambient bubble radius of the maximal response (maximal production rate) is shifted toward the smaller bubble sizes when the acoustic amplitude (wave frequency is fixed) or the ultrasound frequency (acoustic power is fixed) is increased. In addition, it is observed that the increase of wave frequency or the acoustic amplitude decrease cause the range of active bubbles to be narrowed (scenario observation for the four investigated models).