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WANG Yaojun 《声学学报:英文版》1994,(3)
I.IntroductionWiththerapiddevelopmentoffiberreinforeedcompositematerials,muchattcntionhasbeenpaidtothecva1uationofthefiber/matrixinterfaces[1-51wheredefectSmayemergeafterlongusageofthecomposites.Foraweakenedinterface,twostiffnessconstantsareusuallyin-tfoducedtomodc1theboundaryconditionsforthestressesanddisNacementsatbothsidesandtheyareclose1yrclatedtotheultrasonicattenuationduetoscattering['].However,sofarnopublishedrcportsarcavai1ab1e.Whitemadeadetailedinvestigationofsoundwavescatteringatac… 相似文献
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系统研究了La1=3Sr2=3CoO3单相多晶样品在低温下的电磁输运性质和超声特性.电阻率测量表明,La1=3Sr2=3CoO3在整个温区内都表现出金属特性,并且在235 K处电阻率-温度曲线的斜率发生了变化,同时伴随着铁磁相变.超声声速在铁磁相变温度以下出现软化,并在120 K附近达到最小,之后,随着温度的进一步降低,声速开始硬化,同时出现了一个宽大的超声衰减峰.分析认为,该超声异常可能起源于中等自旋态Co3+的Jahn-Teller效应. 相似文献
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In this study, parenchyma cellulose, which was extracted from maize stalk pith as an abundant source of agricultural residues, was applied for preparing cellulose nanoparticles (CNPs) via an ultrasound-assisted etherification and a subsequent sonication process. The ultrasonic-assisted treatment greatly improved the modification of the pith cellulose with glycidyltrimethylammonium chloride, leading to a partial increase in the dissolubility of the as-obtained product and thus disintegration of sheet-like cellulose into nanoparticles. While the formation of CNPs by ultrasonication was largely dependent on the cellulose consistency in the cationic-modified system. Under the condition of 25% cellulose consistency, the longer sono-treated duration yielded a more stable and dispersible suspension of CNP due to its higher zeta potential. Degree of substitution and FT-IR analyses indicated that quaternary ammonium salts were grafted onto hydroxyl groups of cellulose chain. SEM and TEM images exhibited the CNP to have spherical morphology with an average dimeter from 15 to 55 nm. XRD investigation revealed that CNPs consisted mainly of a crystalline cellulose Ι structure, and they had a lower crystallinity than the starting cellulose. Moreover, thermogravimetric results illustrated the thermal resistance of the CNPs was lower than the pith cellulose. The optimal CNP with highly cationic charges, good stability and acceptable thermostability might be considered as one of the alternatively renewable reinforcement additives for nanocomposite production. 相似文献
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In this study, an examination on the spectral, microstructural, and magnetic characteristics of Eu–Nd double-substituted Ba0.5Sr0.5Fe12O19 hexaferrites (Ba0.5Sr0.5NdxEuxFe12−2xO19 (x = 0.00–0.05) HFs) fabricated by an ultrasonic-assisted approach has been presented. An UZ SONOPULS HD 2070 ultrasonic homogenizer with frequency of 20 kHz and power of 70 W was used. The chemical bonding, structure and the morphology of the products were evaluated by Fourier-Transform Infrared (FT-IR) Spectroscopy, XRD (X-ray diffraction), scanning and transmission electron microscopy and techniques. The textural properties of the prepared nanomaterials were examined by using the Brunauer-Emmett-Teller (BET) method. The magnetic properties were studied using a vibrating sample magnetometer (VSM) at room temperature (RT) and low temperature 10 K. The magnitudes of various magnetic parameters including Ms (saturation magnetization), Mr (remanence) and Hc (coercivity) were estimated and evaluated. The M-H loops revealed the hard ferrimagnetic nature for all products at both temperatures. The Ms and Mr values showed a decreasing tendency with increasing degree of Eu3+ and Nd3+ substitutions whereas Hc values displayed an increasing trend. At RT, Ms, Mr and Hc values lie in the ranges of 63.0–68.8 emu·g−1, 24.6–39.2 emu·g−1 and 2252.4–2782.1 Oe, respectively. At 10 K, the values of Ms, Mr and Hc lie between 87.5–97.1 emu·g−1, 33.5–40.1 emu·g−1 and 2060.6–2417.2 Oe, respectively. The observed magnetic properties make the prepared products promising candidates to be applied in the recording media. 相似文献
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In this study, we proposed ‘switching ultrasonic amplitude’ as a new strategy of applying ultrasonic energy to prepare a hybrid of buckminsterfullerene (C60) and gallium oxide (Ga2O3), C60/Ga2O3. In the proposed method, we switched the ultrasonic amplitude from 25% to 50% (by 5% amplitude per 10 min, within 1 h of ultrasonic irradiation) for the sonochemical treatment of a heterogeneous aqueous mixture of C60 and Ga2O3 by a probe-type ultrasonic horn operating at 20 kHz. We found that compared to the conventional techniques associated with high amplitude oriented ultrasonic preparation of functional materials, switching ultrasonic amplitude can better perform in preparing C60/Ga2O3 with respect to avoiding titanium (Ti) as an impurity generating from the tip erosion of a probe-type ultrasonic horn during high amplitude ultrasonic irradiation in an aqueous medium. Based on SEM/EDX analysis, the quantity of Ti (wt.%) in C60/Ga2O3 prepared by the proposed technique of switching ultrasonic amplitude was found to be 1.7% less than that prepared at 50% amplitude of ultrasonic irradiation. The particles of C60/Ga2O3 prepared by different modes of amplitude formed large (2–12 μm) aggregates in their solid phase.Whereas, in the aqueous medium, they were found to disperse in their nano sizes. The minimum particle size of the as-synthesized C60/Ga2O3 in an aqueous medium prepared by the proposed method of switching ultrasonic amplitude reached to approximately 467 nm. Comparatively, the minimum particle sizes were approximately 658 nm and 144 nm, using 25% and 50% amplitude, respectively. Additionally, Ga2O3 went under hydration during ultrasonic irradiation. Moreover, due to the electron cloud interference from C60 in the hybrid structure of C60/Ga2O3, the vibrational modes of Ga2O3 were Raman inactive in C60/Ga2O3. 相似文献
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In this paper, a new type of soluble polyester/silica (PE/SiO2) hybrid was prepared by the ultrasonic irradiation process. The coupling agent γ-glycidyloxypropyltrimethoxysilane (GOTMS) was chosen to enhance the compatibility between the polyester (PE) and silica (SiO2). Furthermore, the effects of the coupling agent on the morphologies and properties of the PE/SiO2 hybrids were investigated using UV-vis and FT-IR spectroscopies and FE-SEM. The densities and solubilities of the PE/SiO2 hybrids were also measured. The results show that the size of the silica particle was markedly reduced by the introduction of the coupling agent, which made the PE/SiO2 hybrid films become transparent. Furthermore, thermal stability, residual solvent in the membrane film and structural ruination of membranes were analyzed by thermal gravimetric analysis (TGA). The effects of SiO2 nanoparticles on the glass transition temperature (Tg) of the prepared nanocomposites were studied by differential scanning calorimetry (DSC). Moreover, their mechanical properties were also characterized. It can be observed that the Young's moduli (E) of the hybrid films increase linearly with the silica content. The results obtained from gas permeation experiments with a constant pressure setup showed that adding SiO2 nanoparticles to the polymeric membrane structure increased the permeability of the membranes. 相似文献