Synthesis of magnetic layered double hydroxide (Fe3O4@CuCr-LDH) decorated with ZIF-8 for efficient sonocatalytic degradation of tetracycline.

A series of Fe3O4@CuCr-LDH hybrids decorated with different amount of ZIF-8 (FLZ, 10-40 wt%) was prepared using simple methods and characterized with different techniques. The activity of the synthesized nanocomposites was investigated in the sonocatalytic degradation of tetracycline (TC) antibiotic from wastewater. When the content of ZIF-8 in the nanocomposite structure was 20 wt%, the FLZ-20 sonocatalyst exhibited the high performance in the sonocatalytic removal of TC. At optimum conditions (0.7 g/L catalyst dosage, pH of 7, 50 mg/L initial concentration of antibiotic, and 15 min sonication time) of the sonocatalytic removal of TC approached to 91.4% under ultrasonic irradiation (USI) using FLZ-20. This efficiency was much higher than those of obtained results by Fe3O4@CuCr-LDH and pristine ZIF-8. The formed ●OH and ●O2- exhibited the major roles in the sonocatalytic TC degradation process. The excellent performance of FLZ-20 can be attributed to the heterojunctions created between composite components, which could improve the electron transfer ability and effectively separate e-/h+ pairs. In addition, FLZ-20 showed the superior reusability and stability during three successive recycling. Moreover, the facile magnetically separation of the sonocatalyst from the aqueous solution was another outstanding feature, which prevents the formation of secondary pollutants. It can be concluded that the fabrication of heterojunctions is an efficient procedure to promote the sonocatalytic acting of the catalyst.

Synergistic effects of layered Ti3C2TX MXene/MIL-101(Cr) heterostructure as a sonocatalyst for efficient degradation of sulfadiazine and acetaminophen in water.

In this work, different mass loadings of MXene-coupled MIL-101(Cr) (MXe/MIL-101(Cr)) nanocomposites were generated through a hydrothermal process in order to investigate the potential of this nanocomposite as a novel sonocatalyst for the elimination of sulfadiazine (SD) and acetaminophen (AAP) in aqueous media. The sonocatalytic activity of different MXe/MIL-101(Cr) compositions and surface functionalities was investigated. In addition, the sonocatalytic activities at various pH values, temperatures, pollutant concentrations, catalyst dosages, initial H2O2 concentrations, and organic matter contents were investigated. The experiments on the sonocatalytic elimination of SD and AAP revealed that MXe/MIL-101(Cr) exhibited a catalytic efficiency of âˆ¼ 98% in 80 min when the MXene loading was 30 wt% in the nanocomposite. Under optimized reaction conditions, the degradation efficiency of MXe/MIL-101(Cr) reached 91.5% for SD and 90.6% for AAP in 60 min; these values were 1.2 and 1.8 times greater than those of MXene and MIL-101(Cr), respectively. The high surface area of the MXe/MIL-101(Cr) nanocomposite increased from 4.68 m2/g to 294.21 m2/g, and the band gap of the tagged MIL-101(Cr) on the MXene surface was minimized. The superior sonocatalytic activity of MXe/MIL-101(Cr) was attributed to the effective contact interface, the effective separation rate of e- - h+ pairs through the type II heterostructure interface, and the favorable high free •OH radical production rates that promoted the degradation of SD and AAP. The solid heterointerface between MIL-101(Cr) and MXene was confirmed through Raman and FTIR analysis and was found to promote accessible •OH radical production under sonication, thus maximizing the catalytic activity of nanocomposites. The present results present an effective strategy for the design of a highly efficient, low-cost, reliable sonocatalyst that can eradicate pharmaceutical pollutants in our environment.

Recyclable MXene-bridged Z-scheme NiFe2O4/MXene/Bi2WO6 heterojunction with enhanced charge separation for efficient sonocatalytic removal of ciprofloxacin.

Sonocatalysis has emerged as a promising technology for addressing environmental pollution issues. However, the efficacy of sonocatalytic processes is primarily hindered by challenges related to the sluggish flow rate of photogenerated electrons. This study presents a novel approach to address this issue by developing an improved Z-scheme NiFe2O4/MXene/Bi2WO6 (NMB) composite that exhibits exceptional sonocatalytic activity for ciprofloxacin (CIP) degradation. In particular, the NiFe2O4/MXene (5 wt%)/Bi2WO6 composite could achieve high CIP (at 10 mg/L) degradation efficiency (97.39 %) after 60 min of ultrasonic irradiation. The exceptional sonocatalytic activity of the composite was attributed to the synergistic interaction of the Z-scheme heterojunction charge transfer route and the electron mediator of Ti3C2-MXene, which enhances light collection capacity, separates photogenerated carriers efficiently, and improves redox activity of the composite. The scavenging experiments reveal that the sonocatalytic degradation of CIP was driven by holes (h+), hydroxyl radicals (•OH), and superoxide anion radicals (•O2-), with the former playing a dominant role. The results of reuse experiments demonstrate the outstanding sonocatalytic stability of the catalyst, as well as its uncomplicated recovery. The developed NMB Z-scheme composite shows promise for sonocatalytic treatment of antibiotics in industrial wastewaters, particularly those with high turbidity and/or low transparency. The findings also open up avenues for developing efficient and cost-effective sonocatalysts with good recyclability and remarkable performance.

Titanium-based MAX-phase with sonocatalytic activity for degradation of oxytetracycline antibiotic.

In light of growing environmental concerns over emerging contaminants in aquatic environments, antibiotics in particular, have prompted the development of a new generation of effective sonocatalytic systems. In this study, a new type of nano-laminated material, Ti2SnC MAX phase, is prepared, characterized, and evaluated for the sonocatalytic degradation of oxytetracycline (OTC) antibiotic. A variety of identification analyses, including X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectrometry, Brunauer-Emmett-Teller, and diffuse reflectance spectroscopy, were conducted to determine the physicochemical properties of the synthesized catalyst. By optimizing the operating factors, total degradation of OTC occurs within 120 min with 1 g L-1 catalyst, 10 mg L-1 OTC, at natural pH of 7.1 and 150 W ultrasonic power. The scavenger studies conclude that the singlet oxygen and superoxide ions are the most active species during the sonocatalytic reaction. Based on the obtained data and GC-MS analysis, a possible sonocatalytic mechanism for the OTC degradation in the presence of Ti2SnC is proposed. The catalyst reusability within eight consecutive runs reveals the proper stability of Ti2SnC MAX phase. The results indicate the prospect for MAX phase-based materials to be developed as efficient sonocatalysts in the treatment of antibiotics, suggesting a bright future for the field.

Sonocatalytic degradation of ciprofloxacin and organic pollutant by 1T/2H phase MoS2 in Polyvinylidene fluoride nanocomposite membrane.

The development of recyclable catalysts with effective properties and stable reusability is great importance for the removal of different types of pollutants in wastewater. Herein, we have synthesized Polyvinylidene fluoride (PVDF) polymer and mixed-phase 1T/2H MoS2 for immobilizing the sonocatalyst material. Techniques such as FESEM, XRD, FTIR, XPS, and UV-vis spectra have been used for analyzing the structural, and morphological properties. The formation of a 1T/2H mixed phase in MoS2 has been revealed by XRD and XPS analysis. Consequently, the sonocatalytic performance of the nanocomposite membrane was investigated through ciprofloxacin (CIP) and organic pollutants (Rhodamine B (RhB)). As a result, MoS2/PVDF (PM4) nanocomposite membrane exhibited a superior sonocatalytic activity with 94.37% and 84.37% of RhB and CIP degradation efficiency with pseudo-first-order kinetic constant (k) of 0.0187 min-1, and 0.0044 min-1. The sonocatalytic property of the nanocomposite membrane is related to 1T/2H mixed-phase and PVDF. Additionally, the metallic based 1T phase MoS2 helps to promote electrons and holes and reduce the recombination rate. Moreover, it promotes the generation of more hydroxy radicals (.OH), and superoxide radicals (∙O2-) play a significant role in sonocatalytic degradation of RhB pollutants. Thus, the improved sonocatalytic degradation of 1T/2H MoS2/PVDF composite membrane exhibited its application in real-time wastewater treatment.

Efficient sonocatalytic degradation of heavy metal and organic pollutants using CuS/MoS2 nanocomposites.

Eco-friendly and highly effective catalysts are receiving considerable attention for the removal of heavy-metal ions and organic pollutants. In this study, we developed CuS/MoS2 nanocomposite sonocatalysts to enhance the degradation rate of environmental contaminants by harnessing ultrasonic irradiation. The successful synthesis of nanocomposite sonocatalysts was confirmed by X-ray diffraction (XRD) analysis, and energy-dispersive X-ray spectroscopy. The incorporation of CuS into MoS2 resulted in a flower-like structure with an increased surface area. Importantly, the sonocatalytic efficiency was enhanced by increasing CuS concentration in the nanocomposites, achieving maximum removal efficiencies of 99% and 88.52% for rhodamine B (RhB) and Cr(VI), respectively. In addition, they showed excellent stability and recyclability over five consecutive cycles, without noticeable changes in the nanocomposite structure. Reactive oxygen species (ROS) used for the degradation were identified using ROS scavengers. We believe that this strategy of exploiting nanocomposite sonocatalysts has a great potential in the field of environmental catalysis.

Sonochemical activation-assisted biosynthesis of Au/Fe3O4 nanoparticles and sonocatalytic degradation of methyl orange.

In this research, a sonochemical activation-assisted biosynthesis of Au/Fe3O4 nanoparticles is proposed. The proposed synthesis methodology incorporates the use of Piper auritum (an endemic plant) as reducing agent and in a complementary way, an ultrasonication process to promote the synthesis of the plasmonic/magnetic nanoparticles (Au/Fe3O4). The synergic effect of the green and sonochemical synthesis favors the well-dispersion of precursor salts and the subsequent growth of the Au/Fe3O4 nanoparticles. The hybrid green/sonochemical process generates an economical, ecological and simplified alternative to synthesizing Au/Fe3O4 nanoparticles whit enhanced catalytic activity, pronounced magnetic properties. The morphological, chemical and structural characterization was carried out by high- resolution Scanning electron microscopy (HR-SEM), Energy Dispersive X-Ray Spectroscopy (EDS) and X-Ray diffraction (XRD), respectively. Ultraviolet-visible (UV-vis) and X-ray photoelectron (XPS) spectroscopy confirm the Au/Fe3O4 nanoparticles obtention. The magnetic properties were evaluated by a vibrating sample magnetometer (VSM). Superparamagnetic behavior, of the Au/ Fe3O4 nanoparticles was observed (Ms = 51 emu/g and Hc = 30 Oe at 300 K). Finally, the catalytic activity was evaluated by sonocatalytic degradation of methyl orange (MO). In this stage, it was possible to achieve a removal percentage of 91.2% at 15 min of the sonocatalytic process (160 W/42 kHz). The initial concentration of the MO was 20 mg L-1, and the Fe3O4-Au dosage was 0.075 gL-1. The MO degradation process was described mathematically by four kinetic adsorption models: Pseudo-first order model, Pseudo-second order model, Elovich and intraparticle diffusion model.

Design and performance of a novel direct Z-scheme NiGa2O4/CeO2 nanocomposite with enhanced sonocatalytic activity.

A novel direct Z-scheme NiGa2O4/CeO2 nanocomposite was designed and prepared via simple sol-hydrothermal and calcination methods, and its sonocatalytic activity was tested by studying the degradation of a model antimicrobial agent, malachite green (MG), under ultrasonic irradiation. Near complete (96.2%) degradation of MG (at 10 mg/L) could be achieved by the NiGa2O4/CeO2 nanocomposite (at 1.0 g/L) after ultrasonic irradiation (40 kHz, 300 W) for 60 min at 25 °C. Under the same conditions, only 51.2 and 72.0% of the MG degraded in the presence of NiGa2O4 and CeO2 (at 1.0 g/L), respectively. These results demonstrate that the direct Z-scheme NiGa2O4/CeO2 nanocomposite has excellent sonocatalytic activity, which is attributed to the matching band-gaps between NiGa2O4 and CeO2. The sonocatalytic activity of NiGa2O4/CeO2 nanocomposite decreased by 17% after four cycles of reuse, which is indicative of relatively good reusability. Scavenging experiments revealed that sonocatalytic degradation of MG results from the combined action of hydroxyl radicals (OH) and holes (h+), with the latter having a greater contribution. The pathways and mechanism of MG degradation were proposed based on the degradation intermediates detected. The results demonstrate that the prepared direct Z-scheme NiGa2O4/CeO2 nanocomposite worked as designed and exhibited high and stable sonocatalytic activity during MG degradation, and could thus serve as a promising candidate in sonocatalytic treatment of other organic pollutants in wastewaters. The findings also provide new insights on the mechanism of sonocatalytic degradation and the design of efficient Z-scheme sonocatalysts.

Ultrasonic degradation of selected dyes using Ti3C2Tx MXene as a sonocatalyst.

MXene, a new family of two dimensional materials, was utilized as a sonocatalyst in an ultrasonic treatment (US) process for removal of methylene blue (MB) and acid blue 80 (AB). The physico-chemical properties of MXene were characterized using scanning electron microscopy, transmission electron microscopy, porosimetry, and a zeta potential analyzer. Degradation of dyes by US was systemically investigated under several experimental conditions including: power density of US (45, 90, 135, and 180 W L-1), frequency of US (28 and 970 kHz), pH of dye solution (3.5, 7, and 10.5), solution temperature (293, 303, and 313 K), and addition of hydroxyl radical promotor (H2O2) and scavenger (t-BuOH) to concentrations of 25 mM. Based on the experimental results, the quantity of H2O2, which was used as an indicator of hydroxyl radical concentration, was an important factor in determining the degradation rate of MB and AB in this US study. Additionally, synergetic indices for removal of both dyes were higher than 1.0 in all cases, indicating the outstanding efficiency of MXene as a sonocatalyst in the US reactor for removal of both, due to an increase in both (i) the quantity of H2O2 in the US reactor and (ii) active sites for adsorbates from dispersion effects. A stability test on MXene in the US process was conducted using X-ray diffraction and five-cycle recycling performance tests. Based on our experimental data, MXene can be utilized as a sonocatalyst in the US process for a high removal rate for dyes (e.g., MB).

Biosynthesized Fe- and Ag-doped ZnO nanoparticles using aqueous extract of Clitoria ternatea Linn for enhancement of sonocatalytic degradation of Congo red.

Nowadays, the current synthesis techniques used in industrial production of nanoparticles have been generally regarded as nonenvironmentally friendly. Consequently, the biosynthesis approach has been proposed as an alternative to reduce the usage of hazardous chemical compounds and harsh reaction conditions in the production of nanoparticles. In this work, pure, iron (Fe)-doped and silver (Ag)-doped zinc oxide (ZnO) nanoparticles were successfully synthesized through the green route using Clitoria ternatea Linn. The optical, chemical, and physical properties of the biosynthesized ZnO nanoparticles were then analyzed by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), UV-Vis diffuse reflectance spectroscopy (DRS), zeta potential measurement, Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and surface analysis. The biosynthesized ZnO nanoparticles were crystallized with a hexagonal wurtzite structure and possessed smaller particle sizes than those of commercially or chemically produced samples. The existence of biomolecules to act as reducing and stabilizing agents from C. ternatea Linn aqueous extract was confirmed using FTIR analysis. The biosynthesized ZnO nanoparticles mainly comprised of negatively charged groups and responsible for moderately stable dispersion of the nanoparticles. All these properties were favorable for the sonocatalytic degradation of Congo red. Sonocatalytic activity of ZnO nanoparticles was studied through the degradation of 10 mg/L Congo red using ultrasonic irradiation at 45 kHz and 80 W. The results showed that the sonocatalytic degradation efficiency of Congo red in the presence of biosynthesized ZnO nanoparticles prepared at 50 °C for 1 h could achieve 88.76% after 1 h. The sonocatalytic degradation efficiency of Congo red in the presence of Ag-doped ZnO was accelerated to 94.42% after 10 min which might be related to the smallest band gap energy (3.02 eV) and the highest specific surface area (10.31 m2/g) as well as pore volume (0.0781 cm3/g). Lastly, the biosynthesized ZnO nanoparticles especially Ag-doped ZnO offered significant antibacterial potential against Escherichia coli which indicated its ability to inhibit the normal growth and replication of bacterial cells. These results affirmed that the biosynthesized ZnO nanoparticles could be used as an alternative to the current chemical compounds and showed a superior sonocatalytic activity toward degradation of Congo red.

Enhancement of sonocatalytic degradation of organic dye by using titanium dioxide (TiO2)/activated carbon (AC) derived from oil palm empty fruit bunch.

A novel titanium dioxide/activated carbon (TiO2/AC) composite where AC derived from oil palm empty fruit bunch (EFB) was synthesised by using sol-gel method. All the samples were characterised by using X-ray diffraction (XRD), scanning electron microscopy-energy dispersive X-ray (SEM-EDX), Fourier transformed infrared (FTIR), thermogravimetric analysis (TGA) and surface analyser. SEM analysis showed that TiO2 particles were successfully embedded and well distributed on the AC surface. The elemental composition analysis found that the TiO2/AC composite contained titanium (Ti), oxygen (O) and carbon (C) atoms. Meanwhile, the appearance of new band at about 960 cm-1 which assigned to the Ti-O stretching was observed in the FTIR spectra when the AC was incorporated into TiO2. TGA analysis showed that the weight loss of 32 wt.% from 150 to 550 °C was due to the decomposition of amorphous carbon layers and loss of hydroxyl groups on TiO2. It was found that the TiO2/AC composite had better performance in the sonocatalytic degradation of malachite green as compared to the individual AC and TiO2 because the TiO2/AC composite had dual functionality and huge number of active sites which could promote the mass transfer of dye molecules towards catalyst surface. By using 1.5 g/L of TiO2/AC composite which calcined at 700 °C on 100 mL of 200 mg/L of malachite green at solution pH of 7, a degradation efficiency of 87.11% had been achieved after 30 min of ultrasonic irradiation. A lower chemical oxygen demand (COD) removal (81.75%) was observed because the structured dye molecules underwent mineralisation process during the sonocatalytic degradation to generate intermediate compounds. The TiO2/AC composite was able to be recycled and still achieved a high degradation efficiency of 76.78% after second catalytic cycle as compared to the fresh TiO2/AC composite with degradation efficiency of 87.11%. In conclusion, the TiO2/AC composite had high reusability and promising for practical applications in textile industry.

Eu-doped ZnO nanoparticles: Sonochemical synthesis, characterization, and sonocatalytic application.

Undoped and europium (III)-doped ZnO nanoparticles were prepared by a sonochemical method. The prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS) analysis. The crystalline sizes of undoped and 3% Eu-doped ZnO were found to be 16.04 and 8.22nm, respectively. The particle size of Eu-doped ZnO nanoparticles was much smaller than that of pure ZnO. The synthesized nanocatalysts were used for the sonocatalytic degradation of Acid Red 17. Among the Eu-doped ZnO catalysts, 3% Eu-doped ZnO nanoparticles showed the highest sonocatalytic activity. The effects of various parameters such as catalyst loading, initial dye concentration, pH, ultrasonic power, the effect of oxidizing agents, and the presence of anions were investigated. The produced intermediates of the sonocatalytic process were monitored by GC-Mass (GC-MS) spectrometry.

Preparation of a novel Z-scheme KTaO3/FeVO4/Bi2O3 nanocomposite for efficient sonocatalytic degradation of ceftriaxone sodium.

In this work, a novel Z-scheme sonocatalyst, KTaO3/FeVO4/Bi2O3, is prepared via ultrasonic-assisted isoelectric point method. The prepared samples are characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS) and photoluminescence (PL) spectroscopy. The catalytic activity of Z-scheme KTaO3/FeVO4/Bi2O3 sonocatalyst is studied in degradation of ceftriaxone sodium under ultrasonic irradiation. In addition, the influences of ultrasonic irradiation time, scavengers and sonocatalyst used times on sonocatalytic degradation of ceftriaxone sodium are examined. Under the experimental conditions of 150 min ultrasonic irradiation time, 1.00 g/L KTaO3/FeVO4/Bi2O3 addition amount and 10.00 mg/L ceftriaxone sodium concentration, the sonocatalytic degradation ratio of ceftriaxone sodium achieves 81.30%. Finally, the possible sonocatalytic degradation mechanism of ceftriaxone sodium caused by Z-scheme KTaO3/FeVO4/Bi2O3 sonocatalyst is proposed. The enhanced sonocatalytic activity may be attributed to the fact that the FeVO4 as a special conductive channel provides a strong driving force to transfer electrons through valence state changes of iron and vanadium, which accelerates electron transfer from conduction band (CB) of Bi2O3 to valence band (VB) of KTaO3. Perhaps, the KTaO3/FeVO4/Bi2O3 composite is an excellent Z-scheme sonocatalyst which can be used to effectively degrade the organic pollutants in wastewater under ultrasonic irradiation.

Enhanced sonocatalytic degradation of carbamazepine and salicylic acid using a metal-organic framework.

A metal-organic framework (MOF) was used as a sonocatalyst for ultrasonic (US) processes, to improve the degradation of two selected pharmaceutical active compounds (PhACs); carbamazepine (CBM) and salicylic acid (SA). The intrinsic characteristics of the MOF were characterized using a porosimeter (N2-BET) and scanning electron microscope (SEM). Various experiments were carried out under conditions with different US frequencies (28 and 1000 kHz), US power densities (45-180 W L-1), pH conditions (3.5, 7, and 10.5), and temperatures (293, 303, and 313 K) to investigate the degradation rates of the selected PhACs. Improved removal rates of PhACs were demonstrated within 60 min at 28 kHz (46% for SA; 47% for CBM) and 1000 kHz (60% for SA; 99% for CBM) with an MOF concentration of 45 mg L-1 in the US/MOF system, in comparison to 28 kHz (20% for SA; 25% for CBM) and 1000 kHz (37% for SA; 97% for CBM) under the 'US only' process. The removal of CBM was greater than that of SA under all experimental conditions due to the intrinsic properties of the PhACs. The degradation rates of PhACs are related to the quantity of H2O2; degradation is thus mostly affected by OH oxidation, which is generated by the dissociation of water molecules. The advantages of the 'US/MOF system' are as follows: (i) dispersion of MOF by US can improve sites and reactivity with respect to adsorption between the adsorbate (PhACs) and the adsorbent (MOF), and (ii) dispersed MOF acted as additional nuclei for water molecule pyrolysis, leading to the production of more OH. Therefore, based on the synergy indices, which were calculated using the removal rate constants [k1 (min-1)] of the pseudo-first order kinetic model, the 'US/MOF system' can potentially be used to treat organic pollutants (e.g., PhACs).

Construction of coated Z-scheme Pd-BaZrO3@WO3 composite with enhanced sonocatalytic activity for diazinon degradation in aqueous solution.

The coated Z-scheme Pd-BaZrO3@WO3 composite as a new-type sonocatalyst with highly sonocatalytic performance is first constructed through sol-gel and hydro-thermal synthesis methods. The chemical configuration, structure and component are characterized by a series of characterization methods. The sonocatalytic degradation of diazinon as a model pollutant is studied to estimate the sonocatalytic performance of coated Z-scheme Pd-BaZrO3@WO3 composite. Some affecting factors such as Pd-BaZrO3 and WO3 mass proportions, ultrasonic (US) irradiation time, reusability and catalyst dosage are researched in detail through UV-vis spectra and gas chromatography (GC). The produced intermediates are detected in the degradation process of diazinon by using gas chromatography-mass spectrometer (GC-MS). The possible reaction mechanism of coated Z-scheme Pd-BaZrO3@WO3 sonocatalyst in sonocatalytic degradation process is also explored. Subsequently, the hydroxyl radicals (OH) and holes (h+) are discriminated to further elaborate the possible sonocatalytic mechanism. The experimental results manifest that the coated Z-scheme Pd-BaZrO3@WO3 sonocatalyst displays a preeminent sonocatalytic performance under ultrasonic irradiation because it can efficaciously suppress recombination of electrons (e-) and holes (h+), extend light response scope and provide almost 100% oxidization surface. In addition, the introduced palladium (Pd) nanorods connecting BaZrO3 and WO3 can expedite e- transfer. Under optimal conditions, the most of diazinon molecules can be disintegrated in the existence of the coated Z-scheme Pd-BaZrO3@WO3 under ultrasonic irradiation for 150 min. This study provides a feasible method for the treatment of environmental pollutions.

Performance of SiO2/Ag Core/Shell particles in sonocatalalytic degradation of Rhodamine B.

In this study, SiO2/Ag Core/Shell nanoparticles was prepared and sonocatalytic activity of prepared catalyst was investigated by using Rhodamine B as model contaminant, at 35 kHz using ultrasonic power of 160 W within 90 min. The change in efficiency in the sonocatalytic degradation of Rhodamine B catalyzed by SiO2/Ag Core/Shell nanoparticles with respect to the initial concentration of dye, catalyst amount and temperature were firstly investigated. Optimal conditions were found as follows: catalyst amount = 15 mg/L, Temperature = 25 °C and initial concentration of dye = 10 ppm. Influence factors such as pH of solution, O2 saturation of solution and the concentration of H2O2 added to the solution, on degradation efficiency in presence of catalyst, were investigated. SiO2/Ag Core/Shell nanoparticles showed higher sonocatalytic activity at pH = 7 with respect to acidic and alkaline conditions. Degradation efficiency was reached up to 67% in experiments which air pumped (0.6 L/min) through the solution with in 90 min. It was observed that the dye removal increased via increase while H2O2 concentration lower than 10 mM. Higher concentration of H2O2 than the optimal concentration had adverse effect on degradation efficiency. Our results showed that the SiO2/Ag Core/Shell nanoparticles were active catalyst for sonocatalytic degradation of dyes. Reusability of the catalyst was investigated.

One-step hydrothermal synthesis of N/Ti3+ co-doping multiphasic TiO2/BiOBr heterojunctions towards enhanced sonocatalytic performance.

N/Ti3+ co-doping multiphasic TiO2/BiOBr heterojunctions (NT-TBx) were prepared by one-step in situ hydrothermal processes. The crystal phase, morphology, component, and optical properties of the heterojunctions were characterized by X-ray diffraction, scanning electron microscope, transmission electron microscope, X-ray photoelectron spectroscopy, and Ultraviolet-visible diffuse reflectance spectroscopy techniques, respectively. The as-prepared samples exhibit better sonocatalytic activity for the degradation methylene blue, Rhodamine B, and p-Nitrophenol aqueous solution compared with pristine TiO2 and N/Ti3+ co-doping multiphasic TiO2. Especially, the highest degradation ratio of methylene blue was achieved for NT-TB0.3 up to 98.2% after 50 min under ultrasonic irradiation. The high sonocatalytic activity has been kept after four cycles with the tiny decline, indicating the excellent stability of the as-prepared samples. The improvement of sonocatalytic activity could be attributed to the formation of doping level and multiphasic TiO2/BiOBr heterojunctions, which account for the absorption of long wavelength light and the electron-hole pair separation, respectively. Furthermore, superoxide radical (O2-) was demonstrated to be the main reactive species for the degradation of methylene blue under ultrasonic irradiation. This study provides a facile fabrication procedure for N/Ti3+ co-doping multiphasic TiO2/BiOBr heterojunctions and demonstrates an efficient route to promote the application of TiO2 in addressing environment-related issues.

Sonocatalytic degradation of carbamazepine and diclofenac in the presence of graphene oxides in aqueous solution.

This research investigated the removal of carbamazepine (CBZ) and diclofenac (DCF) in water using ultrasonic (US) treatment in the absence or presence of graphene oxides (GOs). Three frequencies and three pH conditions were tested (28, 580, and 1000 kHz and 3.5, 7, and 9.5, respectively). Regarding the effects of US frequency and pH, 580 kHz and pH 3.5 were more effective at removing CBZ and DCF (>86% for CBZ and >92% for DCF) than 1000/28 kHz and pH 7/9.5 within 60 min. However, sonocatalytic removal was enhanced in the presence of GOs; more than 99% CBZ and DCF removal was achieved at 580 kHz and pH 3.5 within 40 min. The sonicated GOs were more stable at 28 kHz than at higher frequencies of 580 and 10,00 kHz. The adsorption of CBZ and DCF has increased when GOs were sonicated at 28 kHz (44% and 61%, respectively) compared with 580 kHz (34% and 52%, respectively) and 1000 kHz (18% and 39%, respectively). The negative charges of GOs increased at 28 kHz (-105.1 mV), however, it decreased at higher frequencies such as 580 kHz (-71.5 mV) and 1000 kHz (-58.6 mV), which led to increased electrostatic repulsion that increased the stability of the GO particles in water. The overall enhancement in CBZ and DCF removal was due to an increase in cavitational bubbles, which in turn led to increased production of OH• and enhanced adsorption due to dispersion (resulting from US irradiation), which caused an increase in active adsorption sites of the GOs.

Sonocatalytic activity of a heterostructured ß-Bi2O3/Bi2O2CO3 nanoplate in degradation of bisphenol A.

Novel heterostructured ß-Bi2O3/Bi2O2CO3 nanoplates (hBN) were synthesized to observe the sonocatalytic degradation of bisphenol A (BPA) (widely used as a model pollutant) under ultrasonic (US) irradiation. Prior to obtaining the hBN, the Bi2O2CO3 micropowder precursor was prepared under hydrothermal conditions and then converted to hBN by increasing the calcination temperature to 300 °C. The synthesized hBN samples were characterized by field emission scanning electron microscope with energy dispersive X-ray analysis (FESEM/EDX), transmission electron microscopy (TEM), X-ray diffraction (XRD), ultraviolet-visible spectrophotometer diffuse reflection spectroscopy (UV-vis DRS), and X-ray photoelectron spectroscopy (XPS). The hBN/US system exhibited greater sonocatalytic activity for the degradation of BPA than the US treatment with the single element bismuth oxide, ß-Bi2O3 prepared by annealing the Bi2O2CO3 precursor at 400 °C for 1 h. The US frequency and US power intensity in the hBN/US system were the key operating parameters, which were responsible for the complete degradation of BPA during 6 h of reactions. The degradation efficiency of BPA under the US irradiation was positively correlated with the dose of hBN. Our findings indicate that heterostructured hBN can be used as an efficient sonocatalyst for the catalytic degradation of BPA in water and wastewater treatment.

Ultrasound assisted synthesis of WO3-ZnO nanocomposites for brilliant blue dye degradation.

The present work deals with the preparation of WO3 and WO3-ZnO nanocomposites in presence of ultrasonic irradiation, and its use in the sonocatalytic degradation of brilliant blue dye. WO3-ZnO nanocomposite is prepared using one step in-situ ultrasound assisted method. The successfully prepared WO3 and WO3-ZnO nanocomposites were characterized using different characterization techniques such as XRD, Raman, BET, FE-SEM and EDS. The XRD pattern reveals that the formation of monoclinic and hexagonal crystal structures of WO3 and ZnO respectively. BET study shows that WO3-ZnO nanocomposite have maximum surface area than that of the WO3. EDS study confirms the formation of WO3-ZnO nanocomposites. Further the use of the prepared WO3 and WO3-ZnO nanocomposites as a sonocatalyst for the degradation of brilliant blue dye. The rate constant (k) was evaluated as a function of the initial concentration of brilliant blue dye. It is found that WO3-ZnO nanocomposites exhibits maximum sonocatalytic activity as compared to WO3 photocatalyst.