Sonochemiluminescence of lucigenin using amines as coreactant: Reactivity and mechanism studies

Sonochemiluminescence (SCL) from aqueous solution of lucigenin (Luc²⁺) has been studied using aliphatic amines as coreactant. The SCL intensity are strongly dependent on the dissolved gases such as air, oxygen, nitrogen and argon. The most strong SCL signals are observed from oxygen saturated alkaline solution containing Luc²⁺ when small amount of trialkylamine, such as tripropylamine (TPrA) was added into the solution. In an ultrasonic field, TPrA can adsorb onto the cavitation bubble/solution interface where TPrA is oxidized by OH to form a radical cation TPrA⁺ and subsequently produce a highly reducing TPrA species through a deprotonation reaction of the TPrA⁺. TPrA is suggested to initiate the reduction reactions of Luc²⁺ and molecule oxygen to produce Luc⁺ and superoxide radical anion (O₂⁻), respectively. The radical-radical coupling reaction between Luc⁺ and O₂⁻ is expected to initiate the light emission. The production of O₂⁻ is examined by spectrofluorometric method using 2-(2-pyridyl)benzothiazoline as a fluorescent probe. The results show that the production of O₂⁻ by ultrasound was more efficient in oxygen saturated solution in the presence of coreactants, consistent with the results with SCL measurements.     

Hybrid solvothermal/sonochemical-mediated synthesis of ZnO NPs generative of OH radicals: Photoluminescent approach to evaluate OH scavenging activity of Egyptian and Yemeni Punica granatum arils extract

Zinc oxide NPs were synthesized solvothermally within sonochemical mediation and characterized by XRD, FTIR, SEM, EDX, elemental mapping, TEM and UV–vis. spectrophotometry. To evaluate the hydroxyl radicals (OH) scavenging activity of arils extract of Egyptian (EGY-PAM) and Yemeni Punica granatum (YEM-PAM), the developed zinc oxide nano particles (ZnO NPs) as a highly productive source of hydroxyl radicals (under Solar-illumination) was used. The yield of OH was trapped and probed via fluorimetric monitoring. This suits the first sensitive/selective photoluminescent avenue to evaluate the OH scavenging activity. The high percentage of DPPH radical scavenging reflected higher contents of phenolics, flavonoids, and anthocyanins that were found in EGY-PAM and YEM-PAM. Although, some secondary metabolites contents were significantly different in EGY-PAM and YEM-PAM, the traditional DPPH radical scavenging methodology revealed insignificant IC₅₀. Unlike, the developed fluorimetric probing, sensitively discriminated the OH scavenging activity with IC₅₀ (105.7 µg/mL) and lower rate of OH productivity (k = 0.031 min⁻¹) in case of EGY-PAM in comparison to IC₅₀ (153.4 µg/mL) and higher rate of OH productivity (k = 0.053 min⁻¹) for YEM-PAM. Our findings are interestingly superior to the TBHQ that is synthetic antioxidant. Moreover, our developed methodology for fluorimetric probing of OH radicals scavenging, recommends EGY-PAM as OH radicals scavenger for diabetic patients while YEM-PAM exhibited a better OH radicals scavenging appropriate for high blood pressure patients. More interestingly, EGY-PAM and YEM-PAM exhibited high anticancer potentiality. The aforementioned OH and DPPH scavenging activities as well as the anticancer potentiality present EGY-PAM and YEM-PAM as promising sources of natural antioxidants, that may have crucial roles in some chronic diseases such as diabetics and hypertension in addition to cancer therapeutic protocols.     

Application of persulfate with hydrodynamic cavitation and ferrous in the decomposition of pentachlorophenol

Hydrodynamic cavitation (HC) and Fe(II) are advanced oxidation processes, in which pentachlorophenol (PCP) is treated by the redox method of activating persulfate (PS). The kinetics and mechanism of the HC and Fe(II) activation of PS were examined in aqueous solution using an electron spin resonance (ESR) spin trapping technique and radical trapping with pure compounds. The optimum ratio of Fe(II)/PS was 1:2, and the hydroxyl radical (HO) and sulfate radical (SO₄⁻) generation rate were 5.56 mM h⁻¹ and 8.62 μM h⁻¹, respectively. The generation rate and R_ct of HO and SO₄⁻ at pH 3 and 50 °C in the Fe(II)/PS/HC system are 7584.6 μM h⁻¹, 0.013 and 24.02 μM h⁻¹, 3.95, respectively. The number of radicals was reduced as the pH increased, and it increased with increasing temperature. The PCP reaction rate constants was 4.39 × 10⁻² min⁻¹ at pH 3 and 50 °C. The activation energy was 10.68 kJ mol⁻¹. In addition, the mechanism of PCP treatment in the Fe(II)/PS/HC system was a redox reaction, and the HO⁻/SO₄⁻ contribution was 81.1 and 18.9%, respectively. In this study, we first examined PCP oxidation through HO and SO₄⁻ quantification using only the Fe(II)/PS/HC process. Furthermore, the results provide the foundation for activation of PS by HC and Fe(II), but also provide a data basis for similar organic treatments other than PCP.     

Sonochemical dosimetry: A comparative study of Weissler,Fricke and terephthalic acid methods

Acoustic cavitation and sonochemical reactions play a significant role in various applications of ultrasound. A number of dosimetry methods are in practice to quantify the amount of radicals generated by acoustic cavitation. In this study, hydroxyl radical (OH) yields measured by Weissler, Fricke and terephthalic acid dosimetry methods have been compared to evaluate the validities of these methods using a 490 kHz high frequency sonochemical reactor. The OH yields obtained after 5 min sonication at 490 kHz from Weissler and Fricke dosimetries were 200 µM and 289 µM, respectively. Whereas, the OH yield was found to be very low (8 µM) when terephthalic acid dosimetry was used under similar experimental conditions. While the results agree with those reported by Iida et al. (Microchem. J., 80 (2005) 159), further mechanistic details and interfering reactions have been discussed in this study. For example, the amount of OH determined by the Weissler and Fricke methods may have some uncertainty due to the formation of HO₂ in the presence of oxygen. In order to account for the major discrepancy observed with the terephthalic acid dosimetry method, high performance liquid chromatography (HPLC) analysis was performed, where two additional products other than 2-hydroxy terephthalic acid were observed. Electrospray ionization mass spectrometry (ESI-MS) analysis showed the formation of 2,5-dihydroxyterephthalic acid as one of the by-products along with other unidentified by-products. Despite the formation of additional products consuming OH, the reason for a very low OH yield obtained by this dosimetry could not be justified, questioning the applicability of this method, which has been used to quantify OH yields generated not only by acoustic cavitation, but also by other processes such as γ-radiolysis. The authors are hoping that this Opinion Paper may initiate further discussion among researchers working in sonochemistry area that could help resolve the uncertainties around using these dosimetry methods.     

Production and dispersion of free radicals from transient cavitation Bubbles: An integrated numerical scheme and applications

As an advanced oxidation process with a wide range of applications, sonochemistry relies on acoustic cavitation to induce free radicals for degrading chemical contaminants. The complete process includes two critical steps: the radical production inside the cavitation bubble, and the ensuing dispersion of these radicals into the bulk solution. To grasp the physicochemical details in this process, we developed an integrated numerical scheme with the ability to quantitatively describe the radical production-dispersion behavior. It employs coupled simulations of bubble dynamics, intracavity chemical reactions, and diffusion–reaction-dominated mass transport in aqueous solutions. Applying this method to the typical case of argon and oxygen bubbles, the production mechanism for the main radicals is revealed. Moreover, the temporal-spatial distribution of the radicals in the liquid phase is presented. The results demonstrate that the enhanced radical production observed in oxygen bubbles can be traced to the initiation reaction O₂ + H₂O → OH+HO₂, which requires relatively low activation energy. In the outside liquid region, the dispersion of radicals is limited by robust recombination reactions. The simulated penetration depth of OH is around 0.2 μm and agrees with reported experimental measurements. The proposed numerical approach can be employed to better capture the radical activity and is instrumental in optimizing the engineering application of sonochemistry.     

Sonozonation (sonication/ozonation) for the degradation of organic contaminants – A review

Ozonation (OZ) is an important advanced oxidation process to purify water and wastewater. Because of the lower solubility and instability of ozone (O₃), selective oxidation and dependence on pH value, the industrial applications of OZ have been hindered by the following disadvantages: incomplete removal of pollutants, lower mineralization efficiency and the formation of toxic by-products. Meanwhile, OZ seems to have higher processing costs than other technologies. To improve the treatment efficiency and O₃ utilization, several combined processes, such as H₂O₂/O₃, UV/O₃, and Cavitation/O₃, have been explored, while the combined method of ultrasonication (US) with OZ is a promising treatment technology with a complex physicochemical mechanism. In US alone, the sonolysis of water molecules can produce more powerful unselective oxidant hydroxyl radicals (OH), and directly cause the sonochemical pyrolysis of volatile pollutants. In US/OZ, US can promote the mass transfer of O₃, and also drive the chemical conversion of O₃ to enhance the formation of OH. Various layouts of US/OZ devices and the interactive effects of US/OZ (synergism or antagonism) on the degradation of various organics are illustrated in this review. The main factors, including US frequency, pH value, and radical scavengers, significantly affect the mass transfer and decomposition of O₃, the formation of OH and H₂O₂, the degradation rates of organics and the removal efficiencies of COD and TOC (mineralization). As a result, US can significantly increase the yield of OH, thereby improving the degradation efficiency and mineralization of refractory organics. However, US also enhances the decomposition of ozone, thereby reducing the concentration of O₃ in water and impairing the efficiency of selective oxidation with O₃ molecules.     

Enhanced electrochemical decontamination and water permeation of titanium suboxide reactive electrochemical membrane based on sonoelectrochemistry

Reactive electrochemical membrane (REM) allows electrochemical oxidation (EO) water purification under flow-through operation, which improves mass transfer on the anode surface significantly. However, O₂ evolution reaction (OER) may cause oxygen bubbles to be trapped in small-sized confined flow channels, and thus degrade long-term filterability and treatability of REM. In this study, ultrasound (ultrasonic vibrator, 28 kHz, 180 W) was applied to EO system (i. e. sonoelectrochemistry) containing titanium suboxide-REM (TiSO-REM) anode for enhanced oxidation of 4-chlorophenol (4-CP) target pollutant. Both experimental and modeling results demonstrated that ultrasound could mitigate the retention of O₂ bubbles in the porous structures by destructing large-size bubbles, thus not only increasing permeate flux but also promoting local mass transfer. Meanwhile, oxidation rate of 4-CP for EO with ultrasound (EO-US, 0.0932 min⁻¹) was 216% higher than that for EO without ultrasound (0.0258 min⁻¹), due to enhanced mass transfer and OH production under the cavitation effect of ultrasound. Density functional theory (DFT) calculations confirmed the most efficient pathway of 4-CP removal to be direct electron transfer of 4-CP to form [4-CP]⁺, followed by subsequent oxidation mediated by OH produced from anodic water oxidation on TiSO-REM anode. Last, the stability of TiSO-REM could be improved considerably by application of ultrasound, due to alleviation of electrode deactivation and fouling, indicated by cyclic test, scan electron microscopy (SEM) observation and Fourier transform infrared spectroscopy (FT-IR) characterization. This study provides a proof-of-concept demonstration of ultrasound for enhanced EO of recalcitrant organic pollutants by REM anode, making decentralized wastewater treatment more efficient and more reliable.     

Enhanced piezoelectric-induced catalysis of SrTiO3 nanocrystal with well-defined facets under ultrasonic vibration

Facet engineering of nanocomposite has been confirmed to be an efficient strategy to accelerate their catalytic performances, but to improve their piezoelectric catalytic activities by facet engineering has been seldom reported. Herein, we developed a series of SrTiO₃ nanocrystals with exposed {0 0 1} facet, dominant {1 1 0} facet and co-exposed {0 0 1} and {1 1 0} facets, respectively, and firstly revealed its piezoelectric catalytic performance under ultrasonic vibration. Moreover, the relationship between piezoelectric-induced catalytic activity and facet-dependence of SrTiO₃ nanocrystal was disclosed for the first time. The SrTiO₃ nanocrystal with co-exposed {0 0 1} and {1 1 0} facets exhibited effectively enhanced piezoelectric catalytic activity by degrading Rhodamine B (RhB) under ultrasonic vibration, as compared to that of SrTiO₃ nanocrystals with exposed {0 0 1} facet and dominant {1 1 0} facet, respectively. In addition, trapping experiments and active species quantitative experiments confirmed that the co-exposed {0 0 1} and {1 1 0} facets were beneficial to produce O₂⁻ and OH with the generation rates of 8.3 and 132.2 μmol g⁻¹ h⁻¹, respectively. The OH radical played a dominant role in piezoelectric catalytic process. Finally, the piezoelectric catalysis mechanism of SrTiO₃ surface heterojunction was proposed based on a DFT study. This study presents an in-depth understanding of piezoelectric-induced catalytic of perovskite nanocrystals with exposed well-defined facets.     

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 (P_A: 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 P_A = 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).     

Synergistic,aqueous PAH degradation by ultrasonically-activated persulfate depends on bulk temperature and physicochemical parameters

Coupling ultrasound with other remediation technologies has potential to result in synergistic degradation of contaminants. In this work, we evaluated synergisms from adding high-power ultrasound (20 kHz; 250 W) to activated persulfate over a range of bulk temperatures (20–60 °C). We studied the aqueous degradation kinetics of three polycyclic aromatic hydrocarbons (PAHs: naphthalene, phenanthrene, and fluoranthene) treated by ultrasound-alone, heat-activated persulfate, and combined ultrasonically-activated persulfate (US-PS). At 20 °C, observed US-PS rate constants strongly correlated with Wilke-Chang diffusion coefficients. This correlation indicates PAH molecules diffuse to the bubble-water interface prior to reaction with sulfate radicals (SO₄⁻) generated at the interface. At higher temperatures, observed US-PS rate constants appear to be a more complicated function of temperature and diffusion coefficients. Synergy indexes for PAHs with fast diffusion coefficients were greatest at 20 °C. Fluoranthene, the largest and most hydrophobic PAH, had a maximum synergy index at 30 °C; it benefited from additional thermal persulfate activation in bulk solution. Fluoranthene synergy indexes, however, decreased above 30 °C and became antagonistic at 60 °C. Electron paramagnetic resonance (EPR) spin trapping was used to quantify hydroxyl radical (OH) produced from acoustic cavitation in the absence of persulfate. These data showed consistent OH production from 20 to 60 °C, indicating PAH antagonisms at 60 °C were not due to lower bubble collapse temperatures. Instead, the results suggest that PAH antagonisms are caused by increased radical–radical recombination as bulk temperature increases. In effort to develop an efficient, combined remediation technology, this work suggests bulk temperatures between 20 and 40 °C maximize US-PS synergisms.     

Assay of hydroxyl radicals generated by focused ultrasound

Water sonolysis leads to the formation of hydroxyl radicals (OH). Various techniques are used to detect the OH production and thus to assess the level of ultrasound-mediated cavitation generated in vitro. In this study, we used terephthalic acid (TA) as an OH trap. This method is based on the fluorescent properties of hydroxyterephthalic acid (HTA) formed by the reaction of TA with OH and used as an indicator of the degree of inertial cavitation caused.The experimental system is comprised mainly of a focused piezoelectric ultrasound transmitter and a measurement cell containing 1X PBS/TA diluted solution. In the first part, we aimed to characterize the most appropriate experimental conditions (TA dosimeter solution, irradiation time) in order to optimize the resulting HTA fluorescence values. Then, we could determine that the HTA production increased with the level of the cavitation phenomenon caused by the acoustic power from which OH production may be estimated.     

Determination of nitrofurans in feeds based on silver nanoparticle-catalyzed chemiluminescence

A highly sensitive chemiluminescence (CL) method for the determination of nitrofurans (NFs) was developed based on the enhancement of CL intensity of luminol–H₂O₂–NFs system by silver nanoparticles (AgNPs). It was supposed that the oxygen-related radicals of OH and superoxide radical (O₂^?) could be produced when NFs reacted with H₂O₂. Furthermore, the enhancement mechanism was originated from the reinforcer of AgNPs, which could catalyze the generation of the OH radical. Then OH radicals reacted with luminol anion and HO₂^? to form luminol radical (L^?) and O₂^?. The excited state 3-aminophthalate anion was obtained in the reaction of L^? and O₂^?, which was the emitter (luminophor) in the luminol–H₂O₂ CL reaction system and the maximal emission of the CL spectrum was at 425 nm. The experiments of scavenging oxygen-related radicals were done to confirm these reactive oxygen species participated in the CL reaction. The limits of detection (LOD) (S/N=3) were 8×10^?7 g mL^?1 for furacilin, 8×10^?8 g mL^?1 for furantoin, 4×10^?8 g mL^?1 for furazolidone and 2×10^?7 g mL^?1 for furaltadone. The proposed method was successfully applied to the determination of NFs in feeds and pharmaceutical samples.     

Mechanistic study on the combination of ultrasound and peroxymonosulfate for the decomposition of endocrine disrupting compounds

The effectiveness and synergistic mechanisms of combining ultrasonic process (US) with peroxymonosulfate (PMS) were investigated using Bisphenol A (BPA) and Dimethyl Phthalate (DMP) as the model pollutants. Synergy between US and PMS improved the degradation of target pollutants, and PMS was found to play a dual role. The optimum dosage of PMS and the extent of efficiency promotion were found to depend on not only the ultrasonic frequency but also on the hydrophobicity of target pollutants. The scavenger quenching experiments and electron paramagnetic resonance analysis indicated that OH was responsible for DMP degradation in both US and US/PMS processes. The chemical probe experiments also proved that activation of PMS could increase the production of OH while excess PMS consumed the available radicals. Furthermore, it was found for the first time that the constituent salts of KHSO₄ and K₂SO₄ in the commercial Oxone also made considerable influence on US/PMS process. It was also found that the combination of US and PMS showed more pronounced synergistic effect for treating DMP at lower concentrations. Higher efficiency was achieved at more acidic condition and similar efficiencies were obtained at pH range of 5.1 ~ 8.12. DMP degradation pathways were found to be the OH addition to the aromatic ring and hydrogen absorption at the aliphatic chains with and without the presence of PMS, but much better mineralization capability was obtained in the presence of PMS than ultrasonic degradation alone.     

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 P_e = 120 W, equivalent to P_A ∼ 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.     

Ultrasound-engineered synthesis of WS2@CeO2 heterostructure for sonocatalytic degradation of tylosin

The main aim of the present investigation was the intercalation of WS₂ nanosheets in the structure of ceria (CeO₂) to be used for the efficient catalytic destruction of tylosin (TYL) as a macrolide antibiotic in water. As-synthesized heterostructured catalyst was placed in a sono-reactor (40 kHz and 300 W) in order to degrade TYL through the sonocatalysis. 15 wt% WS₂/CeO₂ was chosen for performing the systematic experiments. Decreasing the concentration of TYL, along with increasing the WS₂/CeO₂ dosage led to reduced degradation efficiency. The water hardness was demonstrated to be a suppressive agent on the sonocatalysis of the target pollutant. As-generated holes, OH, and also O₂⁻ were responsible for the degradation of TYL. Increasing the ultrasound power and operating temperature enhanced the degradation efficiency. The degradation rate boosted up when the temperature was raised from 10 °C (0.0107 1/min) to 40 °C (0.0165 1/min). Moreover, the lowest activation energy (E_a) for sonocatalytic degradation was obtained as 10.81 kJ/mol. The sonocatalytic activity of WS₂/CeO₂ in the sono-reactor encountered insignificant change within five consecutive operational runs (~15% reduction). The mechanism and pathways of the sonocatalytic decomposition of TYL are also proposed.     

Potential-modulated electrochemiluminescence of a tris(2,2′-bipyridine)ruthenium(II) / lidocaine system under 430 kHz ultrasound irradiation

The electrochemiluminescence (ECL) of tris(2,2′-bipyridine)ruthenium(II) (Ru(bpy)₃²⁺) in the presence of lidocaine was investigated under ultrasound (US) irradiation. The sonoelectrochemical experiments are conducted by indirect irradiation of ultrasound with a piezoelectric transducer operating at 430 kHz. In a supporting electrolyte at pH 11, the Ru(bpy)₃²⁺/lidocaine system gave weak ECL peaks around +1.2 V and +1.45 V, respectively. The ECL signal at +1.2 V was attributed to redox reactions of the oxidative intermediates of Ru(bpy)₃²⁺ and lidocaine, while the signal at +1.45 V was assumed to be caused by an advanced oxidation process due to the generation of hydroxyl radicals (OH) at the electrode surface. In this study, the potential modulation approach is employed in the study of ECL process upon US irradiations because it can suppress the noise components from sonoluminescence effectly and improve the resolution of ECL-potential profiles. It is found ECL signals were greatly enhanced upon US irradiation at the output power of 30 W, however, the relative intensity of ECL signal at +1.2 V was larger than that obtained with a rotating disk electrode even though the mass transport effect is equilvalent. The experiment results suggest that the chemical effect (i.e., generation of OH) by 430 kHz US becomes remarkable in the electrochemical process. Detailed ECL reaction routes under US are proposed in this study.     

Nonstoichiometry of the perovskite-type solid solution La0.9Ca0.1Cr1−yAlyO3−δ

Nonstoichiometry of the perovskite-type solid solutions La_0.9Ca_0.1Cr_1−yAl_yO_3−δ was studied by high-temperature gravimetry under controlled P(O₂) atmospheres of 1–10^− 23 bar at 1073–1273 K. The observed data were described by a regular solution-like model for the randomly distributed defects of V_O¨, Cr_Cr., Ca_La,, and Al_Cr^X. With the increase in y, V_O¨ formation becomes much easier. For y > 0.8, some fraction of Ca_La, becomes surrounded only by Al_Cr^X and V_O¨ remains around such Ca_La, up to high P(O₂) to reduce the maximum oxygen content below 3.000.     

Using pulsed wave ultrasound to evaluate the suitability of hydroxyl radical scavengers in sonochemical systems

Hydroxyl radical (OH) scavengers are commonly used in sonochemistry to probe the site and nature of reaction in aqueous cavitational systems. Using pulsed wave (PW) ultrasound with comparative sonochemistry we evaluated the performance of OH scavengers (i.e., formic acid, carbonic acid, terephthalic acid/terephthalate, iodide, methanesulfonate, benzenesulfonate, and acetic acid/acetate) in a sonochemical system to determine which OH scavengers react only in bulk solution and which OH scavengers interact with cavitation bubbles. The ability of each scavenger to interact with cavitation bubbles was assessed by comparing the pulse enhancement (PE) of 10 μM of a probe compound, carbamazepine (CBZ), in the presence and absence of a scavenger. Based on PE results, acetic acid/acetate appears to scavenge OH in bulk solution, and not interact with cavitation bubbles. Methanesulfonate acts as reaction promoter, increasing rather than inhibiting the degradation of CBZ. For formic acid, carbonic acid, terephthalic acid/terephthalate, benzenesulfonate, and iodide, the PE was significantly decreased compared to in the absence of the scavenger. These scavengers not only quench OH in bulk solution but also affect the cavity interface. The robustness of acetic acid/acetate as a bulk OH scavenger was validated for pH values between 3.5 and 8.9 and acetic acid/acetate concentrations from 0.5 to 0.1 M.     

Analysis of ultrasonic pre-treatment for the ozonation of humic acids

This paper presents an intensification study of an ozonation process through an ultrasonic pre-treatment for the elimination of humic substances in water and thus, improve the quality of water treatment systems for human consumption. Humic acids were used as representative of natural organic matter in real waters which present low biodegradability and a high potential for trihalomethane formation. Ultrasonic frequency (98 kHz, 300 kHz and 1 MHz), power (10–40 W) and sonicated volume (150–400 mL) was varied to assess the efficiency of the ultrasonic pre-treatment in the subsequent ozonation process. A direct link between hydroxyl radical (HO) formation and fluorescence reduction was observed during sonication pre-treatment, peaking at 300 kHz and maximum power density. Ultrasound, however, did not reduce total organic carbon (TOC). Injected ozone (O₃) dose and reaction time were also evaluated during the ozonation treatment. With 300 kHz and 40 W ultrasonic pre-treatment and the subsequent ozonation step (7.4 mg O₃/L_gas), TOC was reduced from 21 mg/L to 13.5 mg/L (36% reduction). HO attack seems to be the main degradation mechanism during ozonation. A strong reduction in colour (85%) and SUVA₂₅₄ (70%) was also measured. Moreover, changes in the chemical structure of the macromolecule were observed that led to the formation of oxidation by-products of lower molecular weight.     

Turning single bubble sonoluminescence from blue in pure water to green by adding trace amount of carbon nanodots

Sonoluminescence (SL) is an interesting physical effect which can convert acoustic energy into light pulses. Up to now, the microscopic mechanism of the SL has not yet been fully clear. It is known that hydroxyl radicals play the important role for SL from water. In this work, we take advantage of carbon nano-dots (CNDs) as free radical captors to modulate the hydroxyl radicals (OH) in SL effect. Through studying the single bubble SL (SBSL) from CND aqueous solution (CNDAS) with trace amount of CNDs, we find that the color of SBSL is tuned dramatically from blue in water to green in CNDAS. Two different SL mechanisms can be identified from emission spectrum. One comes from blackbody-like radiation and another is attributed from the characteristic emission with identified peaks. The decrease in the yield of H₂O₂ in the presence of CNDs suggests the modulation effect on SL via OH interacting with CNDs. By comparison of the CNDs before and after sonication, it is found that hydroxyl radicals generated during SL can take part in the chain-like oxidation of the chemical groups attached to the CNDs to form larger amount of carboxyl groups. The blackbody temperature of blackbody-like radiation decreases from 15,600 K in water to 11,300 K in CNDAS. Moreover, the emission from hydroxyl radicals and two new luminescent centers related to carboxyl groups are introduced in SL from CNDAS. These important and interesting findings indicate that by adding trace amount of CNDs in water, the effect of SBSL can be significantly modulated, which can provide a macroscopic phenomenon for gaining an insight into the microscopic mechanism of the SL effect.