Ultrasound-assisted dispersion of SrFe<Subscript>12</Subscript>O<Subscript>19</Subscript> nanoparticles in organic solvents and the use of the dispersion as magnetic cosmetics

A new method of dispersing the aggregated strontium hexaferrite (SrFe₁₂O₁₉) magnetic nanoparticles in organic solvents such as propylene glycol monomethyl ether acetate (PGMEA), propylene glycol (PG), and glycerol, by an ultrasonic bath is reported herein. The particles size of SrFe₁₂O₁₉ after treatment with the PGMEA is in the range 70–100 nm. The structure of dispersed SrFe₁₂O₁₉ was characterized using transmission electron microscopy (TEM), high resolution scanning electron microscopy (HR SEM) and thermo gravimetric analysis (TGA). This dispersed material was used for the preparation of a topical magnetic cosmetic product as follows: The dispersion of SrFe₁₂O₁₉ in PG was mixed with “Dermud-Ahava Body Cream”, an ‘oil in water’ emulsion of a Dead Sea mineral cosmetic, “AHAVA”, and the magnetic properties of the created composite were determined. The ferrimagnetic behavior of the composite has been demonstrated as being very similar to the behavior of strontium hexaferrite itself.     

Velocity study in an ultrasonic reactor

In order to determine the parameters required to describe and to optimize sonochemical reactors, we have investigated the water flow inside such a reactor. With this aim, the experimental velocity field has been measured by tomography laser. The influence of certain parameters such as the electric power, the water height and the fluid viscosity has been evaluated. At the same time, the water movement has been studied theoretically using Nyborg's model. We have tried to improve this model by considering a three-dimensional velocity.     

超声波作用下的钛醇盐水解法制备纳米TiO2

近十几年来, 有关二氧化钛光催化性能的研究已引起人们的浓厚兴趣, 在此方面进行了大量研究. 目前, 纳米二氧化钛的制备方法主要有化学沉淀法、溶胶-凝胶法、气相法和水热法等[1,2]. 超声化学是近年来新兴的一门边缘交叉学科, 已被应用于制备具有特殊结构和性能的纳米材料, 如金属[3]、碳化物[4]、氮化物[5]、氧化物[6]、合金[7]以及生物材料[8]等, 但对于超声作用在纳米粒子晶型转变方面的研究报道较少.     

Sonochemical preparation of SnS and SnS2 nano- and micropowders and their characterization

Sonochemical production of tin(II) and tin(IV) sulfides is investigated. Different conditions of syntheses are examined: used solvent (ethanol or ethylenediamine), source of tin (SnCl₂ or SnCl₄), the molar ratio of thioacetamide to the tin source, and time of sonication. The obtained powders are characterized by the X-ray diffraction method (PXRD), scanning electron microscopy (SEM), scanning transmission electron microscopy (STEM), energy-dispersive X-ray spectroscopy (EDX), and the Tauc method. Raman and FT-IR measurements were performed for the obtained samples, which additionally confirmed the crystallinity and phase composition of the samples. The influence of experimental conditions on composition (is it SnS or SnS₂), morphology, and on the bandgap of obtained products is elucidated. It was found that longer sonication times favor more crystalline product. Each of bandgaps is direct and most of them show typical values – c.a. 1.3 eV for SnS and 2.4 eV for SnS₂. However, there are some exceptions. Synthesized powders show a variety of forms such as needles, flower-like, rods, random agglomerates (SnS₂) and balls (SnS). Using ethanol as a solvent led to powders of SnS₂ independently of which tin chloride is used. Sonochemistry in ethylenediamine is more diverse: this solvent protects Sn²⁺ cations from oxidation so mostly SnS is obtained, while SnCl₄ does not produce powder of SnS₂ but Sn(SO₄)₂ instead or, at a higher ratio of thioacetamide to SnCl₄, green clear mixture.     

Benzophenone-3 ultrasound degradation in a multifrequency reactor: Response surface methodology approach

Response Surface Methodology was used for optimizing operating variables for a multi-frequency ultrasound reactor using BP-3 as a model compound. The response variable was the Triclosan degradation percent after 10 sonication min. Frequency at levels from 574, 856 and 1134 kHz were used. Power density, pulse time (PT), silent time (ST) and PT/ST ratio effects were also analyzed. 2² and 2³ experimental designs were used for screening purposes and a central composite design was used for optimization. An optimum value of 79.2% was obtained for a frequency of 574 kHz, a power density of 200 W/L, and a PT/ST ratio of 10. Significant variables were frequency and power level, the first having an optimum value after which degradation decreases while power density level had a strong positive effect on the whole operational range. PT, ST, and PT/ST ratio were not significant variables although it was shown that pulsed mode ultrasound has better degradation rates than continuous mode ultrasound; the effect less significant at higher power levels.     

Ultrasound assisted the preparation of 1-butoxy-4-nitrobenzene under a new multi-site phase-transfer catalyst – Kinetic study

In the present research work deals with the preparation of 1-butoxy-4-nitrobenzene was successfully carried out by 4-nitrophenol with n-butyl bromide using aqueous potassium carbonate and catalyzed by a new multi-site phase-transfer catalyst (MPTC) viz., N¹,N⁴-diethyl-N¹,N¹,N⁴,N⁴-tetraisopropylbutane-1,4-diammonium dibromide, under ultrasonic (40 kHz, 300 W) assisted organic solvent condition. The pseudo first-order kinetic equation was applied to describe the overall reaction. Under ultrasound irradiation (40 kHz, 300 W) in a batch reactor, it shows that the overall reaction greatly enhanced with ultrasound irradiation than without ultrasound. The present study provides a method to synthesize nitro aromatic ethers by ultrasound assisted liquid–liquid multi-site phase-transfer catalysis condition.     

One-step sonochemical syntheses of Ni@Pt core–shell nanoparticles with controlled shape and shell thickness for fuel cell electrocatalyst

We demonstrate a facile one-step method to synthesize Ni@Pt core–shell nanoparticles (NPs) with a control over the shape and the Pt-shell thickness of the NPs. By adjusting the relative reactivity of the Pt and Ni reagents in ultrasound-assisted polyol reactions, two Ni@Pt NP samples of the same composition (Ni/Pt = 1) and size (3–4 nm) but with different particle shape (octahedral vs. truncated octahedral) and different Pt-shell thicknesses (1–2 vs. 2–3 monolayer) are obtained. The control is achieved by using different Ni reagents, Ni(acac)₂ (acac = acetylacetonate) and Ni(hfac)₂ (hfac = hexafluoroacetylacetonate). A reaction mechanism that can explain all of the observations is proposed. The Ni@Pt NPs show up to threefold higher mass activity than pure Pt NPs in oxygen reduction reaction. Between the two Ni@Pt NP samples, the one composed of octahedral NPs with the thicker Pt-shell has higher activity than the other.     

Sonocrystallization and sonofragmentation

The application of ultrasound to crystallization (i.e., sonocrystallization) can dramatically affect the properties of the crystalline products. Sonocrystallization induces rapid nucleation that generally yields smaller crystals of a more narrow size distribution compared to quiescent crystallizations. The mechanism by which ultrasound induces nucleation remains unclear although reports show the potential contributions of shockwaves and increases in heterogeneous nucleation. In addition, the fragmentation of molecular crystals during ultrasonic irradiation is an emerging aspect of sonocrystallization and nucleation. Decoupling experiments were performed to confirm that interactions between shockwaves and crystals are the main contributors to crystal breakage. In this review, we build upon previous studies and emphasize the effects of ultrasound on the crystallization of organic molecules. Recent work on the applications of sonocrystallized materials in pharmaceutics and materials science are also discussed.     

Sonochemistry: A good,fast and clean method to promote the synthesis of 5-arylidene-2,4-thiazolidinediones

The efficient synthesis of sixteen 5-arylidene-2,4-thiazolidinediones by aldol condensation reaction of 2,4-thiazolidinedione, mono- and di-substituted arenealdehydes and KOH using ultrasound irradiation is reported. The desired compounds were obtained in a few min (10–30 min) with moderate to good yields (25–81%).     

超声波在催化过程中的应用

简述了声化学效应的作用机理，并综述了超声在催化反应、催化剂的制备及再生过程中的应用。