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A hybrid coating made of poly (methyl methacrylate) with SiO2-TiO2 particles (PMMA/SiO2-TiO2) has been developed for use as a coating on nanosatellites, evaluating its resistance to high vacuum by quantifying its weight loss. The coating was applied on an Al 7075 aluminum substrate used for the aerospace sector. PMMA/SiO2-TiO2 hybrid coatings were prepared using sol-gel reaction in situ assisted with sonochemistry. The SiO2 particles and TiO2 (50:50% wt. of rutile/anatase) particles by tetraethyl orthosilicate (TEOS), and Titanium (IV) Isopropoxide (TIPO). Radical polymerization of methyl methacrylate (MMA) monomer was conducted with (3-mercaptopropyl) trimethoxy silane (3-MPTS) used as a coupling molecular agent, and benzoyl peroxide as a catalyst. The coatings obtained have a thickness of 20 μm which were deposited by blade coating technique on the substrate, obtaining homogeneous and defect-free coatings. Adhesion and hardness were measured using ASTM standards required for this sector. To evaluate its resistance to ultra-high vacuum, it was done as close as possible to the ASTM E-595 norm [1], where it indicates that the coatings must be evaluated at vacuum conditions of 10−5 Torr and 125°C for a period of 24 hours. The coatings were evaluated before and after the test by spectroscopy analysis to determine a possible degradation in the chemical structure. The resulting weight loss not exceeding 0.02%, and the addition of Ti-O-Si particles led to an increase in chemical stability under vacuum conditions without affecting the chemical structure of the highly cross-linked PMMA/Ti-O-Si matrix, which was monitored by FTIR and Raman spectroscopy. [ABSTRACT FROM AUTHOR]

In this work, cerium dioxide nanostructures were synthesized in an easy sonochemical way. CeO2 nanoparticles have received much attention in nanotechnology. CeO2NPs, exhibit biomimetic properties depending on their size, ratio of valency on their surface, and the ambient physico-chemical properties. Nanomedicine has emerged as a promising avenue for targeted cancer therapy, aiming to develop innovative approaches with improved efficacy and reduced side effects. Here, for the production of cerium dioxide nanostructures, a new and natural capping agent called Rosa Damascena extract was utilized, as well as ceric ammonium nitrate as a metal precursor. The results of the characterization of the oxide sample fabricated in the presence of Rosa Damascena extract demonstrated that nanostructures with a sponge-like morphology, which have a pure cubic crystal phase, were formed. The cytotoxicity effect of CeO2 NPs on glioblastoma and neuroblastoma cell lines (T98, SHSY5Y) was studied using the MTT test; cerium oxide nanoparticles exhibited cytotoxicity effects on T98 and SHSY5Y cell lines, compared to the control. The improved cytotoxic effects can be due to the plant secondary metabolites involved in the green synthesis of NPs. Consequently, synthesized CeO2 NPs have revealed an acceptable inhibitory impact upon cancer cell lines. [ABSTRACT FROM AUTHOR]

A sonochemical synthesis of SnS2 quantum dots using acetone as a solvent is investigated. Two different tin sources (SnCl2∙2H2O or SnCl4∙5H2O) as well as two different sulfur sources (thioacetamide or Na2S2O3) were applied. The sonication time was also varied between 60 and 120 min. Resulting products of syntheses were characterized with the following techniques: powder X-ray diffraction, electron microscopy (SEM and HR-TEM), Raman and FT-IR spectroscopies, the Tauc method, and X-ray photoelectron spectroscopy. Obtained SnS2 nanostructures were in the form of quantum dots in the case of synthesis lasting 60 min (size of crystallites in the range of 3.5–7 nm) and in the form of elongated nanorods of length ca. 25–30 nm and width of 5–6 nm in the case of synthesis lasting 120 min. XPS analyses revealed that the surface of the obtained products contained a significant amount of tin at the second oxidation state (i.e., SnS). The quantum dots produced in the synthesis lasting 60 min showed a value of energy bandgap of 2.7 eV indicating potential applications in photocatalysis. [ABSTRACT FROM AUTHOR]

MXene-based (nano)materials have recently emerged as promising solutions for antibiotic photodegradation from aquatic environments, yet they are limited by scalability, stability, and selectivity challenges in practical settings. We formulated Fe2O3-SiO2/MXene ternary nano-photocomposites via coupled wet impregnation and sonochemistry approach for optimised tetracycline (TC) removal (the second most used antibiotic worldwide) from water using response surface methodology-central composite design (RSM-CCD). The photocatalysts containing various loading of Fe2O3/SiO2 (5–45 wt%) on the MXene with a range of calcination temperatures (300–600 °C) via RSM optimisation were synthesised, characterised regarding crystallinity properties, surface morphology, binding energy, and light absorption capability, and analysed for TC degradation efficiency. The 25FeS/MX-450 composite among all samples demonstrated a superior efficiency in TC photocatalytic removal (98%) under optimised conditions (TC degradation: 39.75 mg/L, time: 68.28 min, pH: 5.57, catalyst dosage: 0.75 g/L). The developed surface area, with a reduced band gap due to FeS nanoparticles incorporation with improved light absorption within the visible spectrum, played a crucial role in the 25FeS/MX-450 heterostructure matrix, enhancing photogenerated carriers' separation and transportation capabilities. The tetracycline photoreduction mechanism involved electron transfer from FeS to the surface of MXene, engaging with O2 to produce •O2−, attributed to the high electron mobility of MXene. Our findings for such nano-photocomposites materials can underscore the considerable potential of MXene-based nanomaterials for pharmaceutical removal from waterways. [ABSTRACT FROM AUTHOR]

Ultrasonic irradiation holds potential for the selective oxidation of non‐volatile organic substrates in the aqueous phase by harnessing hydroxyl radicals as chemical initiators. Here, a mechanistic description of hydroxyl radical‐initiated glyoxal oxidation is constructed by gleaning insights from photolysis and radiation chemistry to explain the yields and kinetic trends for oxidation products. The mechanistic description and kinetic measurements reported herein reveal that increasing the formation rate of hydroxyl radicals by changing the ultrasound frequency increases both the rates of glyoxal consumption and the selectivity towards C2 acid products over those from C−C cleavage. Glyoxal consumption also occurs more rapidly and with greater selectivity towards C2 acids under acidic conditions, which favor the protonation of carboxylate intermediates into their less reactive acidic forms. Leveraging such pH and frequency effects is crucial to mitigating product degradation by secondary reactions with hydroxyl radicals and oxidation products (specifically hydrogen peroxide and superoxide). These findings demonstrate the potential of ultrasound as a driver for the selective oxidation of aldehyde functions to carboxylic acids, offering a sustainable route for valorizing biomass‐derived platform molecules. [ABSTRACT FROM AUTHOR]

In this work, a novel strategy for the straightforward synthesis of isoxazolo[5,4‐b]pyridines from a one‐pot reaction of aryl glyoxal, 5‐aminoisoxazoles, and malononitrile under ultrasound (US) irradiation is described. In the reaction, acetic acid has a dual role as solvent and catalyst. The advantages of this reaction include easy purification of products, raw materials with easy access, short reaction time, high efficiency, and green conditions by utilizing ultrasound irradiation as an energy source and using acetic acid as solvent and Lewis acid. The synthesis achieved high yields of isoxazolo[5,4‐b]pyridines with a broad substrate scope, successfully producing twelve diverse derivatives. The methodology capitalizes on the benefits of sonochemistry, which accelerates reaction rates and improves selectivity while minimizing waste. The proposed mechanism involves a series of reactions including Knoevenagel condensation, Michael addition, and subsequent cyclization processes. This approach not only streamlines the synthesis of complex heterocycles but also aligns with environmentally friendly practices. [ABSTRACT FROM AUTHOR]

In this study, gold nanoparticles and graphene oxide nanocomposite-modified electrodes were prepared by the sonochemical method. We evaluated their electrocatalytic activity toward nitric oxide (NO) oxidation and the analytical performance in the determination of NO and demonstrated its improved selectivity in the detection of NO over NO2−. [ABSTRACT FROM AUTHOR]

The textile sector is widely acknowledged as one of the most environmentally damaging sectors globally, primarily due to its high consumption of water and energy, utilization of chemicals, and the discharge of waste water containing a complex mixture of hazardous substances. The incorporation of nanotechnology, particularly through wet processes involving nano finishes, while enhancing textile functionality, further exacerbates these environmental concerns. Consequently, the exploration and promotion of sustainable methodologies are imperative across all wet treatments in textile processing. Among the potential solutions, sonoprocesses stand out as a promising avenue for mitigating resource consumption, and supporting environmentally friendly synthesis and application of nanomaterials to textiles. Sonoprocesses offer the advantage of carrying processes at low temperature and pressure, and the use of aqueous media instead of organic solvents. This comprehensive review delves into the multifaceted applications of sonoprocesses within the textile realm, with a specific emphasis on the synthesis and application of nanomaterials to textiles. Discussing the diverse applications of sonoprocesses, this study will pave the way for the integration of these techniques within the textile industry, ultimately aiming for widespread adoption on a commercial scale. This will help in promoting sustainable practices and reducing the ecological footprint of the textile sector. [ABSTRACT FROM AUTHOR]

Sonochemical synthesis is becoming a popular method of preparing various nanomaterials, including metals, carbons, oxides, and chalcogenides. This method is relatively cheap and responds to the challenges of green chemistry as it typically does not involve high temperatures, high pressures, inert atmospheres, or long reaction times in comparison to other conventional methods. The utilization of ultrasound in synthesis makes the elimination of toxic solvents possible, as well as the execution of the synthesis without the use of reducing and stabilizing agents, while receiving products with the same or even better properties. The application of ultrasound allows for the synthesis of various nanomaterials with different properties for use in fields such as catalysis, electrochemistry, medicine, and biosensors. The final product is influenced by multiple variables such as temperature, pH, reagents, capping agents, time of reaction, and the addition of dopants. [ABSTRACT FROM AUTHOR]

In polymer science, mechanochemistry is emerging as a powerful tool for materials science and molecular synthesis, offering novel avenues for controlled polymerization and post‐synthetic modification. Building upon the previous research, nitroxide‐mediated polymerization (NMP) is merged with mechanochemistry through the design of nitroxide‐based mechanophore macroinitiators, pioneering the first instance of a sonochemical nitroxide‐mediated‐type polymerization. As NMP usually requires high temperatures, this study demonstrates that a sonochemical NMP‐type process allows polymerization under reduced temperatures down to 55 °C. Moreover, depending on the nature of the employed monomers, gelated networks are obtained, demonstrating the adaptability of the mechanophore system. This study elucidates the potential of mechanochemistry in polymer synthesis, offering insights into manipulating polymerization kinetics and advancing materials science applications. [ABSTRACT FROM AUTHOR]

Sonochemistry is a fascinating field that has drawn considerable interest from researchers across different disciplines. One of the key challenges in this field is the accurate characterization of the sonochemical field, which is crucial for understanding the underlying mechanisms and optimizing the process. To address this challenge, researchers have developed various monitoring methods that allow them to measure key parameters such as the intensity, frequency, and distribution of acoustic waves in the sonoreactor. In this review, we focus on the chemical dosimetry techniques that are commonly used for sonochemical monitoring. These techniques have been extensively studied in the literature and are known for their reliability and accuracy. However, as we will see, the performance of these techniques can vary depending on the chemical nature of the probing species and the experimental conditions, highlighting the need for a careful selection and calibration of the monitoring method. We begin by discussing the principles of chemical dosimetry in sonochemistry and how these methods can be used to measure key sono‐acoustic parameters. We then provide a detailed analysis of the various dosimetry techniques, including their advantages, limitations, and applicability under different operating conditions. In summary, our review serves as a valuable resource for researchers seeking to optimize their sonochemical experiments and contribute to the advancement of this fascinating field. [ABSTRACT FROM AUTHOR]

Carbon nanomaterials are a class of low-dimensional materials that have aroused a great deal of interest for decades. Carbon nano-onions (CNOs) are carbon nanomaterials with a wide range of applications. In this study, we report a novel process for synthesizing CNOs from SiC— the only inorganic carbon source—through one-pot sonication in pure water at room temperature. This synthesis process is more facile and can be performed under gentler conditions and lower temperatures than previous methods. The as-synthesized samples were characterized using transmission electron microscopy (TEM), Raman spectroscopy, Fourier-transform infrared spectroscopy (FTIR), and scanning transmission electron microscopy–electron energy loss spectroscopy (STEM-EELS). The TEM results revealed CNOs with diameters of approximately 20– 30 nm, and the FTIR and STEM-EELS results indicated the presence of oxygen-containing functional groups on the CNOs and the growth of carbon from a SiC single crystal. The proposed method for obtaining CNOs from an inorganic carbon source via sonication provides novel insights into the CNO generation mechanism and its functionalization. [ABSTRACT FROM AUTHOR]

ABSTRACT BiOBr nanosheets were loaded onto SnO2 quantum dots, ZnO nanosheets, and SnO2/ZnO‐2 (SZ‐2) to form different heterojunction photocatalysts by sonochemistry, respectively. The photocatalytic activity of the prepared photocatalysts was evaluated by degrading the target dye Rhodamine B (RhB). The results showed that the degradation efficiency of BiOBr/SnO2/ZnO (BSZ) for RhB reached 97.5% at 80 min. The significant increase in catalytic activity of BSZ was attributed to the synergistic and interfacial effects among the three materials. Combined with the radical trapping experiments, it can be concluded that the catalytic mechanism of BSZ as a dual Z‐type heterojunction. [ABSTRACT FROM AUTHOR]

The serotonin 5-HT6 receptor (5-HT6R), expressed almost exclusively in the brain, affects the Cdk5 signaling as well as the mTOR pathway. Due to the association of 5-HT6R signaling with pathways involved in cancer progression, we decided to check the usefulness of 5-HT6R ligands in the treatment of CNS tumors. For this purpose, a new group of low-base 5-HT6R ligands was developed, belonging to arylsulfonamide derivatives of cyclic arylguanidines. The selected group of molecules was also tested for their antiproliferative activity on astrocytoma (1321N1) and glioblastoma (U87MG, LN-229, U-251) cell lines. Some of the molecules were subjected to ADMET tests in vitro, including lipophilicity, drug binding to plasma proteins, affinity for phospholipids, drug–drug interaction (DDI), the penetration of the membrane (PAMPA), metabolic stability, and hepatotoxicity as well as in vivo cardiotoxicity in the Danio rerio model. Two antagonists with an affinity constant Ki < 50 nM (PR 68 Ki = 37 nM) were selected. These compounds were characterized by very high selectivity. An analysis of pharmacokinetic parameters for the lead compound PR 68 confirmed favorable properties for administration, including passive diffusion and acceptable metabolic stability (metabolized in 49%, MLMs). The compound did not exhibit the potential for drug–drug interactions. [ABSTRACT FROM AUTHOR]

Mechanochemistry constitutes a burgeoning field that investigates the chemical and physicochemical alterations of substances under mechanical force. It enables the synthesis of materials which is challenging to obtain via thermal, optical or electrical activation methods. In addition, it diminishes reliance on organic solvents and provides a novel route for green chemistry. Today, as a distinct branch alongside electrochemistry, photochemistry, and thermochemistry, mechanochemistry has emerged as a frontier research domain within chemistry and material science. In recent years, the intersection of mechanochemistry with controlled radical polymerization has witnessed rapid advancements, providing new routes to polymer science. Significantly, we have experienced breakthroughs in methods relying on sonochemistry, piezoelectricity and contact electrification. These methodologies not only facilitate the synthesis of polymers with high molecular weight but also enable precise control over polymer chain length and structure. Transitioning from harsh to mild conditions in mechanochemical routes has facilitated a significant improvement in the controllability of mechanochemical polymerization. From this perspective, we introduce the progress of mechanochemistry in controlled radical polymerization in recent years, aim to clarify the historcial development of this topic. [ABSTRACT FROM AUTHOR]

This study introduces a novel method for hydrogen fuel generation using ultrasound technology through the disassociation of water into hydrogen and oxygen. The proposed experimental setup comprises several key components: a power supply, an ultrasonic generator, two transducers, a reactor vessel, two vapor traps, a condenser, a valve, a hydrogen storage, a humidity sensor and a hydrogen measurement sensor. The system operates at a power of 100 W and a frequency of 40 kHz, and the reactor vessel contains 2L of solution. The study results show a variability in hydrogen production rates under different experimental conditions. The distilled water used in the experiments at 25 °C produces hydrogen at a rate of 0.05 μmol/min, which increases to 0.066 μmol/min at 70 °C. The tap water gives hydrogen production rates ranging from 0.044 μmol/min at 25 °C to 0.06 μmol/min at 70 °C. The lake water produces hydrogen at rates between 0.036 μmol/min and 0.054 μmol/min, while the wastewater ranges from 0.028 μmol/min to 0.044 μmol/min. The present study investigates the effect of CO 2 injection into the sonoreactor on the system performance and shows that hydrogen production rates increase over a 20-min period for the water resources, with higher CO 2 flow rates leading to improved production rates. These findings demonstrate the potential of ultrasound technology for eco-friendly hydrogen production, marking a promising alternative to conventional methods and contributing valuable insights to the field of sustainable energy. [Display omitted] • The study investigates an innovative sonic method of hydrogen generation. • The present system is proposed for clean hydrogen generation. • The experiments are conducted at a frequency of 40 kHz and power of 100 ± 10 W. • The hydrogen generation is tested under various water sources at different temperatures. • The hydrogen generation is assessed by injecting CO 2 into the sonoreactor solution. [ABSTRACT FROM AUTHOR]

Cerium oxide (CeO2), one of the most significant heterogeneous catalysts, has attracted extensive research interest. Herein, ultrafine spherical CeO2 with a diameter of 5 nm is successfully synthesized within a reaction time of 25 min by a simple and environmentally friendly sonochemical method without any additional oxidants or high temperature and pressure conditions, and 50 nm spherical CeO2 was obtained by heat treating the 5 nm spherical CeO2 in 400°C air atmosphere condition for 3 h. By controlling the ultrasonic condition, a specific surface area of up to 194.2 m2/g and a bandgap as low as 2.2 eV are achieved in the CeO2 nanoparticles without any heat treatment. Further study has shown that the as‐prepared spherical CeO2 without heat treatment exhibits remarkable photocatalytic and antibacterial activities under visible light conditions. The study is beneficial for energy conservation in fabricating ultrafine photocatalytic and antibacterial nanomaterials. [ABSTRACT FROM AUTHOR]

A new method to uptake vitamin B12 in aqueous solution as pharmaceutical preparations by adsorption on the solid phase surface by using a multi-layer graphene oxide derivative compounds while the ultrasonic frequency wave was used to increase the efficiency of the extraction of drug from aqueous solution. Interlayer drug extraction conditions were optimized by studying a number of conditions that affect the extraction rate, including pH, ultrasound frequency, residence time of the solution inside the ultrasound device, the effect of the amount of graphene oxide derivative, and vitamin B12 concentration. The effect of temperature was also studied and a number of thermodynamic factors were generated. From the results, it was found that the best weight for the economically useful graphene oxide derivative is 0.01 grams at a concentration of 20 ppm relative to the concentration of the vitamin using an acidic medium of 2.1. The best temperature is 40 0C and within 50 Hz of the frequencies of the ultrasound device during the incubation period of 50 minutes. The proposed method was also applied to pharmaceutical samples containing vitamin B12, and the extraction rate was 95.35 %, with a very small error rate of 0.0465. [ABSTRACT FROM AUTHOR]

Nanoparticles exhibit distinct physical and chemical characteristics and are becoming increasingly significant in the production of innovative nanodevices for many applications in physics, biology, biomedicine, and pharmaceuticals. The aim of this research work is to synthesize Fe (II) and Cu (II) nano-sized complexes of trimethoprim (TMP) using the sonication method, characterize them using physical and spectroscopic methods, and carry out ADMET studies on the synthesized complexes. The spectroscopic and physical studies showed a change in colour and an increase in melting point due to coordination. The novel compounds were slightly soluble in water. The XRD tests revealed that the new nanocomplexes were crystalline. The Fe (II) nanocomplexes had a size of 57.56 nm and the Cu (II) nanocomplexes had a size of 69.88 nm. These values were found using Debye-Scherrer’s equation. The FTIR results of the TMP, Fe (II), and Cu (II) nanometal complexes showed a shift of the amino group band from 3317 to 3295 and 3202 cm−1 and the azomethine band from 1633 to 1625 and 1592 cm−1 in the complexes. In the complexes, the proton NMR spectra revealed an upfield shift of the amine proton. The carbon-13 NMR spectra showed that CH2 was involved in coordination with the metal ions. The spectra studies indicated that TMP coordinated with the metal ions through the methylene and amino groups. A trigonal bipyramid structure was proposed for the complexes. The results of the Rule of 5 studies indicated that the test compounds had a good drug-likeness prediction, with only one violation. The ADMET prediction showed that all of the compounds demonstrated improved pharmacokinetic characteristics and adhered to the RO5 requirement. These findings highlight the therapeutic potential of Fe (II) and Cu (II) nano-sized TMP complexes as bioactive compounds that warrant further investigation for pharmaceutical applications. [ABSTRACT FROM AUTHOR]

Nanoparticle drug delivery systems are precisely designed technologies that utilize nanoparticles to deliver therapeutic drugs to specific targets and regulate their release. In recent times, nanoparticles have garnered significant interest owing to their potential for efficient drug delivery. This work is aimed at synthesizing Fe(II) and Cu(II) nano-sized complexes of sulfamethoxazole (SMX) using the sonication method. The physical and spectroscopic studies showed a colour change from white to grey, and a decrease in melting points suggested the formation of the metal complexes. The nanometal complexes were insoluble in water. XRD analysis showed that the crystallite sizes of Fe(II) and Cu(II) nanometal complexes were determined to be 76.08 nm and 37.13 nm, respectively, using the Debye-Scherrer equation. The FTIR results of the SMX, Fe(II), and Cu(II) nanometal complexes showed a shift of the amine band from 3243 to 3191 cm−1 and the sulfone band from 1154 to 1092 cm−1 in both complexes. The proton NMR showed a shift of the amine proton from 6.100 ppm to 6.035 ppm in the spectra of the Cu(II) complex. The amine chemical shift was absent in the spectra of the Fe(II) complex, showing deprotonation. The carbon-13 NMR spectra showed a similar chemical shift. The spectra studies indicated that SMX coordinated with the metal ions through the amino and sulfone groups. A tetrahedral structure was proposed for the complexes. SMX coordinated as a bidentate ligand to Fe(II) and Cu(II) ions. [ABSTRACT FROM AUTHOR]

This research investigated the performance of bentonite and Al-PILC as catalysts in ethanol conversion to diethyl ether through a dehydration reaction. The natural bentonite was intercalated with the pillaring agent Keggin-ion Al13 to obtain Al-intercalated bentonite. Al-intercalated bentonite has been synthesized using conventional stirring and ultrasonication. Al-intercalated bentonite was calcined at 400 °C for 4 h to produce Al2O3 pillared bentonite (Al-PILC). The dehydration reaction was conducted using a 0.2 g catalyst and 10 mL of ethanol with a nitrogen gas flow rate of 20 mL/min at various reaction temperatures (200, 225, and 250 °C) using a fixed bed microreactor. The characterization results reveal that Al-PILC synthesized by sonochemistry exhibits significantly higher surface area and total acidity values than bentonite and Al-PILC synthesized by conventional methods because of the formation of stable Al2O3 pillars in the interlayer spaces of bentonite. The sonochemically synthesized Al-PILC produces optimum ethanol conversion and diethyl ether yield of 46.05% and 41.11%, respectively. The conversion of ethanol and diethyl ether yield reaches an optimum result at 225 °C. Based on this study, the pillarization of bentonite using Al2O3 can enhance its catalytic properties toward diethyl ether production. [ABSTRACT FROM AUTHOR]

This review article summarises decades of research on nickel hydroxide. Nickel hydroxide is an important material in both physics and chemistry, especially in technical applications such as batteries. First, the structures of two known polymorphs, α-Ni(OH)2 and β-Ni(OH)2, are described. The article also examines common types of disorder in nickel hydroxide, such as hydration, stacking faults, mechanical stresses and the presence of ionic impurities. Related materials such as intercalated α-derivatives and basic nickel salts are also discussed. Various synthetic methods of nickel hydroxide synthesis are reviewed, including chemical and electrochemical precipitation, sol-gel synthesis, chemical ageing, hydrothermal and solvothermal processes, electrochemical oxidation, microwave-assisted techniques and sonochemical methods. The article discusses the physical properties of nickel hydroxide, including its magnetic, vibrational, optical, electrical and mechanical properties. Finally, the article highlights the promising properties of these materials and approaches for the identification and characterization of unknown nickel hydroxide-based samples. [ABSTRACT FROM AUTHOR]

Desulfurization of petroleum derivatives is a topic of interest to researchers because compounds containing sulfur are harmful in the oil refining process and cause problems such as deactivation of catalysts and corrosion in pipelines and refining equipment. In order to improve the efficiency of desulfurization of dibenzothiophene, copper bismuth oxide/reduced graphene oxide (Bi7.38Cu0.62O11.69/rGO) nanocomposite was synthesized by a simple sonochemical method for the first time. The synthesized nanocomposite was identified by FESEM, FT-IR, XRD, DRS, and EDS analyses. Based on XRD analysis, pure copper bismuth oxide is formed using hydrazine, while using sodium hydroxide does not lead to the desired product. FESEM images showed that the size of Bi7.38Cu0.62O11.69 particles decreases in the presence of rGO. The desulfurization results showed that the presence of rGO causes a significant increase in efficiency due to increased light absorption and reduced recombination rate, so that Bi7.38Cu0.62O11.69/rGO nanocomposite has an efficiency of 87%, while pure Bi7.38Cu0.62O11.69 has an efficiency of 68%. Also, it was found that the purity of the copper bismuth oxide has a great effect on the photocatalytic efficiency, so that by calcining the product and removing the impurities, the efficiency increases from 55% to 68%. [ABSTRACT FROM AUTHOR]

There is a growing interest in using green technologies in the food industry. As a green processing technique, ultrasound has a great potential to be applied in many food applications. In this review, the basic mechanism of ultrasound processing technology has been discussed. Then, ultrasound technology was reviewed from the application of assisted food processing methods, such as assisted gelation, assisted freezing and thawing, assisted crystallization, and other assisted applications. Moreover, ultrasound was reviewed from the aspect of structure and property modification technology, such as modification of polysaccharides and fats. Furthermore, ultrasound was reviewed to facilitate beneficial food reactions, such as glycosylation, enzymatic cross-linking, protein hydrolyzation, fermentation, and marination. After that, ultrasound applications in the food safety sector were reviewed from the aspect of the inactivation of microbes, degradation of pesticides, and toxins, as well inactivation of some enzymes. Finally, the applications of ultrasound technology in food waste disposal and environmental protection were reviewed. Thus, some sonoprocessing technologies can be recommended for the use in the food industry on a large scale. However, there is still a need for funding research and development projects to develop more efficient ultrasound devices. [ABSTRACT FROM AUTHOR]

Plastics have become indispensable in modern society; however, the proliferation of their waste has become a problem that can no longer be ignored as most plastics are not biodegradable. Depolymerization/degradation through sustainable processes in the context of the circular economy are urgent issues. The presence of multiple types of plastic materials makes it necessary to study the specific characteristics of each material. This mini-review aims to provide an overview of technological approaches and their performance for the depolymerization and/or degradation of one of the most widespread plastic materials, polypropylene (PP). The state of the art is presented, describing the most relevant technologies focusing on advanced oxidation technologies (AOT) and the results obtained so far for some of the approaches, such as ozonation, sonochemistry, or photocatalysis, with the final aim of making more sustainable the PP depolymerization/degradation process. [ABSTRACT FROM AUTHOR]

Sonochemistry is the use of ultrasonic waves in an aqueous medium, to generate acoustic cavitation. In this context, sonochemistry emerged as a focal point over the past few decades, starting as a manageable process such as a cleaning technique. Now, it is found in a wide range of applications across various chemical, physical, and biological processes, creating opportunities for analysis between these processes. Sonochemistry is a powerful and eco‐friendly technique often called "green chemistry" for less energy use, toxic reagents, and residues generation. It is increasing the number of applications achieved through the ultrasonic irradiation (USI) method. Sonochemistry has been established as a sustainable and cost‐effective alternative compared to traditional industrial methods. It promotes scientific and social well‐being, offering non‐destructive advantages, including rapid processes, improved process efficiency, enhanced product quality, and, in some cases, the retention of key product characteristics. This versatile technology has significantly contributed to the food industry, materials technology, environmental remediation, and biological research. This review is created with enthusiasm and focus on shedding light on the manifold applications of sonochemistry. It delves into this technique's evolution and current applications in cleaning, environmental remediation, microfluidic, biological, and medical fields. The purpose is to show the physicochemical effects and characteristics of acoustic cavitation in different processes across various fields and to demonstrate the extending application reach of sonochemistry. Also to provide insights into the prospects of this versatile technique and demonstrating that sonochemistry is an adapting system able to generate more efficient products or processes. [ABSTRACT FROM AUTHOR]

Jet pump cavitation reactors (JPCRs) have significant potential to be used in water treatment applications. During their operation, the hydroxyl radicals generated by cavitation collapse produce a strong oxidation capacity, which is one of the key mechanisms in disrupting algal cells. In this paper, we investigate the hydroxyl radicals produced by single cavitation bubble in a JPCR. The numerical method includes a bubble dynamic model, molecular diffusion model, energy balance equation, and chemical reaction model for predicting the hydroxyl radical production. Additionally, the pressure distribution within a JPCR is tested and used to analyze the single-bubble performance. The effects of the JPCR operating conditions and structure parameters on hydroxyl radical production are further discussed. Our results indicate that, when the flow rate ratio is positive, the number of hydroxyl radicals is closely related to the development and collapse of the cavitation bubble and reaches a peak value under the critical condition. When the flow rate ratio is negative, the maximum production of hydroxyl radicals appears under backflow stagnation condition. In general, increasing the throat length–diameter ratio and diffuser angle encourages the production of hydroxyl radicals, whereas increasing the area ratio inhibits their generation. [ABSTRACT FROM AUTHOR]

At least 16 bulk polymorphs of linked icosahedrons exist in boron that are not found in other materials, due to the low covalent radius and sp² hybridization capacity of boron atoms. One of them is borophene, an exciting new nanomaterial with a wide range of possible energy uses. The existence of borophene, a two-dimensional (2D) material, has been proven by both theoretical and experimental studies. Borophene's high magnetic conductivity, theoretical specific capacities, and ion transport properties make it a promising candidate in energy applications (EAs). In this study, firstly, the structure, chemical, and physical properties of borophene were mentioned. Then, in terms of synthesis approaches, both top-down and bottom-up techniques such as ultrahigh vacuum (UHV), chemical vapor deposition (CVD), exfoliation by sonochemistry (ExS), molecular beam epitaxy (MBE) and multi-step thermal decomposition (MTD) were discussed. Finally, its use as a catalyst in high-metal-ion batteries, hydrogen storage (HS), nanoelectronics applications hydrogen evolution reaction (HER) was mentioned. [ABSTRACT FROM AUTHOR]

Traditional methods for algae removal in drinking water treatment, such as coagulation and sedimentation, face challenges due to the negative charge on algae cells’ surfaces, resulting in ineffective removal. Ultrasonic cavitation has shown promise in enhancing coagulation performance by disrupting extracellular polymer structures and improving cyanobacteria removal through various mechanisms like shear force and free radical reactions. However, the short lifespan and limited mass transfer distance of free radicals in conventional ultrasonic treatment lead to high energy consumption, limiting widespread application. To overcome these limitations and enhance energy efficiency, advanced carbon-based materials were developed and tested. Nitrogen-doped functional groups on nanodiamond surfaces were found to boost sonosensitivity by increasing the production of reactive oxygen species at the sonosensitizer-water interface. Utilizing low-power ultrasound (0.12 W/mL) in combination with N-ND treatment for 5 min, removal rates of Microcystis aeruginosa cells in water exceeded 90 %, with enhanced removal of algal organic matters and microcystins in water. Visualization through confocal microscopy highlighted the role of positively charged nitrogen-doped nanodiamonds in aggregating algae cells. The synergy between cell capturing and catalysis of N-ND indicates that efficient mass transfer of free radicals from the sonosensitizer’s surface to the microalgae’s surface is critical for promoting cyanobacteria floc formation. This study underscores the potential of employing a low-intensity ultrasound and N-ND system in effectively improving algae removal in water treatment processes.

This research aims to present a sonochemical synthesis method for high-purity willemite nanopowders. Initially, zinc silicate hydrate nanoparticles were created using a modified sonochemistry method in which zinc salts and waterglass were used as starting materials to obtain zinc silicate precipitate under pH-controlled conditions (11–11.5) and Argon gas flux. Following that, the precipitate was heat treated at various temperatures. TGA/DSC, X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), dispersive X-ray spectrometry (EDX), and N2 gas adsorption characterizations were also used to assess phase changes, morphological properties, microstructures, and chemical composition. The formation temperature of a well-crystalline willemite monophase was determined to be 890 °C, and this was supported by XRD analysis. The synthetized material had high homogeneity and excellent purity, according to EDX elemental mapping. Its nanometric nature was further confirmed by microscopic observations (SEM, TEM). Notably, compared to previously reported methods, the aforementioned technique uses a moderate synthesizing temperature, making it economical for mass production and potentially useful in a variety of industrial fields, including ceramics, paints, plastics, biomaterials, and composites, among others. EDX elemental mapping demonstrated high homogeneity and excellent purity of the material. Microscopic observations (SEM, TEM) further confirmed its nanometric character. Notably, the aforementioned method employs a moderate synthesizing temperature compared to previously reported methods, making it cost-effective for mass production with potential applications in various industrial fields, such as ceramics, paints, plastics, biomaterials, and composites, among others. [ABSTRACT FROM AUTHOR]

Cellulose is used widely in antimicrobial packaging due to its abundance in nature, biodegradability, renewability, non-toxicity, and low cost. However, how efficiently and rapidly it imparts high antimicrobial activity to cellulose-based packaging materials remains a challenge. In this work, Ag NPs were deposited on the surface of carboxymethyl cellulose/starch/N'N Methylenebisacrylamide film using ultrasonic radiation. Morphology and structure analysis of as-prepared films were conducted, and the antibacterial effects under different ultrasonic times and reductant contents were investigated. These results showed that Ag NPs were distributed uniformly on the film surface under an ultrasonic time of 45 min. The size of Ag NPs changes as the reducing agent content decreases. The composite film demonstrated a slightly better antibacterial effect against E. coli than against S. aureus. Therefore, this work can provide valuable insights for the research on antimicrobial packaging. [ABSTRACT FROM AUTHOR]

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Ultrasonic baths and sonochemical reactors are widely used in industrial applications dealing with surface cleaning and chemical synthesis. The processes of erosion, cleaning and structuring of the surface can be typically controlled by changing relevant influential parameters. In particular, in this work, we experimentally investigate the effect of NaCl concentration (0-5.5 mol/L) on the erosion of an aluminum foil under ultrasonic exposure at a frequency of 28 kHz. Special attention is paid to the determination of cavitation zones and their visualization using heat maps. It is found that at low NaCl concentration (0.3 mol/L), the foil destruction rate is higher than in distilled water. At higher concentrations of salt, cavitation takes place mainly in the upper part of the container. [ABSTRACT FROM AUTHOR]

Herein a novel gum acacia‐alginate nanogel (GAA) was synthesized via ultrasound‐assisted crosslinking by DPPH and applied for the removal of coomassie brilliant blue (CBB) dye. The fabrication of GAA and its interaction with CBB was specified via FTIR, XRD, SEM, and TEM techniques. The process parameters at which maximum adsorption efficiency, qe (80.12 mg/g), and % efficiency >94 % were achieved include dosage (0.8 g/L), time (80 min), initial dye concentration (20 mg/L), and pH (6). Ultrasound‐assisted uptake was greater than stirring‐assisted due to acoustic cavitation′s hydrodynamic and thermal processes. Pseudo‐second‐order model described the adsorption kinetics and the diffusion mechanism suggested that the rate‐determining step was controlled by both the intraparticle diffusion and the liquid film models. Isotherms showed an excellent fit to the Freundlich model based on higher R2 (0.998) and lower standard error of estimate values (SEE=0.367). The −ΔG° values (−8.152, −8.292, −8.433, −8.586 kJ/mol) indicated that the adsorption process was feasible and spontaneous. The removal of CBB ensued via hydrogen bonding, electrostatic, π‐π, and n‐π interactions. The maximum adsorption capacity of 182.096 mg/g, eco‐friendly characteristics along with regeneration competence depicted that GAA could be effective for scavenging CBB from wastewater. [ABSTRACT FROM AUTHOR]

This comprehensive review delves into the utilization of ultrasound for hydrogen generation, emphasizing the key mechanisms and techniques involved. One of the focal points of the study is the exploration of the generation and detection of cavitation bubbles, which are induced by ultrasound waves. An in-depth overview of various experimental setups that employ ultrasound technology for hydrogen production is also provided. A comparative analysis of these setups reveals differences in crucial parameters such as acoustic intensity, liquid temperature, and frequency. These are the key parameters identified as significant determinants affecting the hydrogen yield and efficiency. This review paper also highlights the potential applications of sonohydrogen as a viable energy resource. While challenges such as the high costs of ultrasound equipment and the need for efficient catalysts exist, the inherent benefits make sonohydrogen a compelling subject for future research and development. The study shows that there is no one-size-fits-all approach, accentuating the importance of understanding these parameters for optimizing the process of hydrogen production. Although the technology is primarily in the experimental phase, existing research indicates that the sonohydrogen production holds considerable potential for large-scale applications. [Display omitted] • The study explores ultrasound's role in enhancing hydrogen production. • The article reviews various experimental setups and comparing them. • The manuscript identifies key parameters affecting sonohydrogen production. • The study discusses the potential dimensions of sonohydrogen options and future research directions. • It examines scaling sonohydrogen production challenges for industrial use. [ABSTRACT FROM AUTHOR]

Sonochemistry under controlled conditions has proven effective in medicinal chemistry and drug development. It can substantially shorten reaction timelines from days or hours to minutes. A convenient one-pot synthesis of 2,4,5-trisubstituted and 1,2,4,5-tetrasubstituted imidazole derivatives catalyzed by PTSA and benzenesulfonic acid in ethanol as solvent, under ultrasonic irradiation and without ultrasound irradiation at 50° C has been achieved successfully. These 2,4,5-trisubstituted and 1,2,4,5-tetrasubstituted imidazole derivatives synthesis were also accomplished using different solvents viz., Methanol, Ethanol, DCM, DMF, Acetonitrile and THF and PTSA as the catalyst. This method yielded the highest % synthesis of 2,4,5-trisubstituted and 1,2,4,5-tetrasubstituted imidazole derivatives with PTSA as the catalyst in solvent ethanol. These reactions were also optimized for % of PTSA catalyst required to obtain the maximum yield of 2,4,5-trisubstituted and 1,2,4,5-tetrasubstituted imidazole derivatives with and without ultrasound irradiation at 50° C. Synthesis of 2,4,5-trisubstituted Imidazole derivatives reaction follows first-order rate kinetics while that of 1,2,4,5-tetrasubstituted Imidazole derivatives reaction follows the second-order rate kinetics. Furthermore, sonochemistry has higher yields, lower cost, easier workups, and higher purity than conventional thermal organic synthesis, which has lower yields, tedious workups, longer reaction periods, lower purity, and numerous byproducts. [ABSTRACT FROM AUTHOR]

1,3,5-triazine derivatives are useful compounds with potential applications in various branches of chemical industry, including pharmaceutical chemistry, cosmetic chemistry, photochemistry, and organic chemistry. Due to the growing environmental requirements on conducting efficient, economical, and safe syntheses, development of new methods for synthesizing organic compounds is highly desirable. In this publication, we present a protocol for the synthesis of 1,3,5-triazine derivatives using a sonochemical approach. In as little as 5 min, it is possible to obtain most of the investigated compounds with a yield of over 75%. An undeniable advantage of this method, besides its short time, is the use of water as the solvent. Furthermore, we provide examples that the sonochemical method may be more versatile than the competing microwave method. Analysis conducted using the DOZNTM 2.0 tool revealed that in terms of the 12 principles of green chemistry, the developed sonochemical method is 13 times “greener” than the classical one. Additionally, it has been demonstrated that the investigated molecules are attractive for their application as drug-like compounds.

Hydrodynamic cavitation (HC) has emerged as a promising technology for water disinfection. Interestingly, when subjected to specific cavitation pressures, jet pump cavitation reactors (JPCRs) exhibit effective water treatment capabilities. This study investigated the cavitation flow and vorticty transport in a JPCR with various area ratios by utilizing computational fluid dynamics. The results reveal that cavitation is more likely to occur within the JPCR as the area ratio becomes smaller. While as the area ratio decreases, the limit flow ratio also decreases, leading to a reduced operational range for the JPCR. During the cavitation inception stage, only a few bubbles with limited travel distances are generated at the throat inlet. A stable cavitation layer developed between the throat and downstream wall during the limited cavitation stage. In this phase, the primary flow carried the bubbles towards the outlet. In addition, it was found that the vortex stretching, compression expansion, and baroclinic torque terms primarily influence the vorticity transport equation in this context. This work may provide a reference value to the design of JPCRs for water treatment.

Sonochemistry contributes to green science as it uses less hazardous solvents and methods to carry out a reaction. In this review, different reactor designs are discussed in detail providing the necessary knowledge for implementing various processes. The main characteristics of ultrasonic batch systems are their low cost and enhanced mixing; however, they still have immense drawbacks such as their scalability. Continuous flow reactors offer enhanced production yields as the limited cognition which governs the design of these sonoreactors, renders them unusable in industry. In addition, microstructured sonoreactors show improved heat and mass transfer phenomena due to their small size but suffer though from clogging. The optimisation of various conditions of regulations, such as temperature, frequency of ultrasound, intensity of irradiation, sonication time, pressure amplitude and reactor design, it is also discussed to maximise the production rates and yields of reactions taking place in sonoreactors. The optimisation of operating parameters and the selection of the reactor system must be considered to each application’s requirements. A plethora of different applications that ultrasound waves can be implemented are in the biochemical and petrochemical engineering, the chemical synthesis of materials, the crystallisation of organic and inorganic substances, the wastewater treatment, the extraction processes and in medicine. Sonochemistry must overcome challenges that consider the scalability of processes and its embodiment into commercial applications, through extensive studies for understanding the designs and the development of computational tools to implement timesaving and efficient theoretical studies.

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.

A green, convenient, and scalable synthesis of alcohols through the reduction of aldehydes and ketones has been developed. The green reduction was conducted using two different methods, namely sonochemistry and mechanochemistry. In the former method, the solution of aldehydes or ketones and sodium borohydride was irradiated under ultrasound irradiation. In the latter technique, the reaction mixture was ground under solvent-free conditions. The reduction reaction was performed at room temperature and completed in only 10 min using both protocols. The results showed that aldehydes and ketones with aromatic, heteroaromatic, and aliphatic motifs were tolerated under the reaction conditions, allowing the formation of the corresponding alcohols with the synthetic yields of 75–98% and 77–95% for grinding and sonication methods, respectively. In addition, the reaction can be carried out on a multigram scale.