圆锥气泡发光的光谱性质

在改进的U型管装置中观察到一种圆锥气泡声致发光现象。声致发光产生的单个光脉冲的能量可达到约1.4 毫焦. 脉冲宽度约100 毫秒。发光光谱由连续光谱上叠加C2,CN,和CH的激发态光谱构成。这种圆锥气泡声致发光为单泡声致发光和多泡声致发光提供了一种联系。     

近似估算法研究磁场与发光气泡耦合机制

以磁场对声致发光影响研究为基础,结合对声致发光时气泡内状态的现有认识,从气泡外、气泡表面及气泡内各层次着手,通过理论估算方法分析磁场与气泡可能存在的各种耦合机制,并对特定磁场条件下两种相互作用能量进行数量估计,评判两者可能存在的各种耦合方式的重要性,进而推测两者相互作用机制.     

利用声致发光成像技术的液体中超声场动态分布的实时测量方法

根据超声空化原理,运用声致发光成像技术测量超声在液体中的动态分布。利用高灵敏度的ICCD成像系统记录水在超声作用下的声致发光图像,并且分析了声致发光的分布和强度与作用超声的关系。结果表明,超声作用下的发光图像能够反映该作用超声在水中的分布情况,从而提出利用声致发光成像技术测量液体中超声场的分布是一种动态测量声场强度的新方法。     

Luminol－碳酸钠水溶液的声致发光

作者用Ｌｕｍｉｎｏｌ－碳酸钠水溶液的声致发光拍摄了预置剪纸图案的照片，同时获得了这种溶液的声致发射光谱和光致荧光光谱。分析表明，由Ｌｕｍｉｎｏｌ增强的碳酸钠水溶液的声致发光主要发生在可见光区域；就声致发光和光致荧光的发射波长而言，这种溶液的声激发和光激发具有一定程度的等效性。     

声致发光

本文介绍了声致发光的研究概况、现行的“热点”机制及其面临的问题,最后指出了研究声致发光的意义。     

乙二醇溶液中圆锥泡声致发光的发光特性

利用一种改进后的U形管圆锥泡声致发光装置，研究了乙二醇溶液中圆锥泡声致发光的发光特性.实验结果表明，利用乙二醇溶液可以得到超强的单个发光脉冲，其脉冲宽度可以达到150 μs，其值远远高于其他方式产生的声致发光的脉冲宽度.测量得到的光谱为一从紫外到可见光波长范围的连续谱，在589 nm附近叠加有钠的3P-3S原子发射谱线.在钠的原子发射谱线两侧测量得到了Na-Ar分子激发态跃迁形成的蓝卫星带，并在声致发光实验中测得了Na-Ar的红卫星带以及钠的3S-4S原子发射谱线. 关键词： 圆锥泡声致发光 光脉冲 光谱 卫星带     

丙三醇溶液声致发光中的黑体辐射谱

利用U型管圆锥泡声致发光装置,测量到了丙三醇溶液中圆锥泡声致发光的光谱和光脉冲。结果表明,测量得到的发光光谱为光滑的连续谱,且与理论模拟得到的黑体辐射谱相吻合,拟合温度分布于2 600～3 500 K范围内。文章从空间和时间两方面分析了圆锥泡空化发光中存在黑体辐射的原因：较大的气泡体积(气泡塌缩半径为1.4 cm)与较长的发光时间(几十微秒)。另外,实验研究表明随着发光波长的增长,光脉冲宽度变宽,从而进一步证明了圆锥泡声致发光中的黑体辐射机制。最后,利用测量得到的发光光谱和脉冲计算得到了发光光强为0.18 J,远远高于其他方式得到的声致发光光强。     

光电倍增管在磷酸液声致发光实验中的应用

对不同厚度液体进行光强测量,深入探索空化气泡的运动,研究发光机理很有意义。用超声激励法在磷酸液体中实现多泡声致发光,研究不同共振频率下发光的特点。利用光电倍增管多次测量发光强度相互比较,结果是在液体厚度10 cm、驱动频率f=21.061kHz和f=20.316kHz时,周期性较好为50μs,液体通过漩涡集中气泡可以使更多气泡发光;在液体厚度3 mm、驱动频率f=17.91kHz和f=19kHz时,周期性很好为25μs;且光信号都较强。结论是磷酸中声致发光强度、周期与液体厚度、驱动频率密切相关。本文以磷酸液多泡声致发光实验研究为基础,从内部和外部原理来出发,详细介绍了光电倍增管在多泡声致发光光强测量中的实用,为今后研究者提供了一些经验。根据实验过程中遇到的一些实际问题提出了建议和改善意见。     

水体中溶解氧对声致发光的影响

采用声源频率为1.1 MHz的超声波, 在温度为283～313 K的范围内引发水中的声致发光, 发现声致发光强度的对数lnI和水中的溶解(DO)的浓度之间呈线性关系。同时模拟了水中含有5种阴离子: Cl-, SO-₄, F-, NO-₃, HCO-₃时阴离子的存在对声致发光的影响, 发现上述5种阴离子对声致发光强度没有影响。     

在ZnS场致发光磷光体形成过程中Cu_2S相的作用

硫化锌磷光体的场致发光性能是因为在这些磷光体中有第二相——硫化铜的存在,这一推测到目前为止,无论从间接的或是直接的方面都得到了证实。在制备ZnS场致发光磷光体的过程中形成Cu_2S,现在已是无可争议的事实。可是Cu_2S参与ZnS磷光体场致发光激发过程的性质还不太清楚。 磷光体中这个相的含量和它对场致发光的作用之间的关系等有关资料可能对查明Cu_2S在场致发光磷光体中的作用有促进作     

Sonoluminescence

Abstract

Sonoluminescence is the light emission phenomenon from collapsing bubbles in liquid irradiated by an ultrasonic wave. In the present review, theoretical and experimental studies of the two types of sonoluminescence [single‐bubble sonoluminescence (SBSL) and multibubble sonoluminescence (MBSL)] are described. SBSL is a sonoluminescence from a single stably pulsating bubble trapped at the pressure antinode of a standing ultrasonic wave. MBSL is a sonoluminescence occurring from many bubbles in liquid irradiated by an ultrasonic wave. The theoretical and experimental studies suggest that SBSL originates in emissions from plasma inside the heated bubble at the bubble collapse, whereas MBSL originates both in emissions from plasma and in chemiluminescence inside heated bubbles at the bubble collapse. Unsolved problems of sonoluminescence have also been explained in detail.     

Opacity and transport measurements reveal that dilute plasma models of sonoluminescence are not valid

A strong interaction between a nanosecond laser and a 70?μm radius sonoluminescing plasma is achieved. The overall response of the system results in a factor of 2 increase in temperature as determined by its spectrum. Images of the interaction reveal that light energy is absorbed and trapped in a region smaller than the sonoluminescence emitting region of the bubble for over 100?ns. We interpret this opacity and transport measurement as demonstrating that sonoluminescencing bubbles can be 1000 times more opaque than what follows from the Saha equation of statistical mechanics in the ideal plasma limit. To address this discrepancy, we suggest that the effects of strong Coulomb interactions are an essential component of a first principles theory of sonoluminescence.     

Multibubble sonoluminescence pulses from Na atoms in viscous liquid

Multibubble sonoluminescence pulses of Na and continuum emissions were measured from NaCl-ethylene glycol solution saturated with Xe at 28 kHz. The Na emission consisted of multiple-peak pulses and single pulses. The intrinsic pulse width estimated from single pulses was 0.37 ns, which differs from 10-165 ns obtained by previous work. High-speed shadowgraphs of bubble dynamics and high-speed movies (32000 fps) of sonoluminescence were observed. The observations suggest that the multiple-peak pulse is due to the superposition of single peaks resulting from bubbles fragmented from a characteristic bubble which repeats the fragmentation and coalescence. This phenomenon may be specific to viscous liquids.     

Mie scattering and the physical mechanisms of sonoluminescence

We propose an experimental procedure to investigate possible mechanisms for radiation emission in sonoluminescence. Our analysis is based on Mie's theory of light scattering for a coated sphere in an external medium. Depending on the physical mechanism responsible of sonoluminescence, the dielectric constant of the hot spot changes. As a case study we consider the problem of the detection of an inner plasma core in sonoluminescent bubbles. Our results show that polarization measurements of scattered light should discern the presence of a plasma provided that light detectors are fast enough. Extensions to other emission mechanisms are briefly discussed.     

Luminescence mechanism of acoustic and laser-induced cavitation

A new approach is proposed for explaining the experimental data on sonoluminescence of acoustic and laser-induced cavitation bubbles. It is suggested that two different sonoluminescence mechanisms, namely, thermal and electric ones, are possible and that they manifest themselves depending on the bubble dynamics. An intense thermal luminescence occurs as a result of compression of an individual stationary spherical bubble; a weak electric luminescence accompanies the deformation and splitting of the bubble when thermal luminescence is suppressed (for example, in the case of multibubble sonoluminescence). It is shown that, when an individual bubble loses its spherical shape under the effect of different actions (change in the acoustic pressure, artificial deformation, translatory motion, etc.) or when a laser-induced bubble undergoes fragmentation, the sonoluminescence spectrum exhibits specific bands that are similar to the bands in the multibubble sonoluminescence spectrum. The appearance of these bands is attributed to the suppression of the thermal sonoluminescence mechanism and the manifestation of the electric mechanism. It is shown that the maximum temperature T _max characterizing the compression of a laser-induced bubble is primarily determined by the temperature of the plasma at the instant of the laser-induced breakdown, whereas, for an acoustic bubble, T _max is primarily determined by the acoustic and hydrostatic pressures and by the saturation vapor pressure of the liquid.     

Computational simulation of ionization processes in single-bubble and multi-bubble sonoluminescence

The most recent spectroscopic studies of moving-single bubble sonoluminescence (MSBSL) and multi-bubble sonoluminescence (MBSL) have revealed that hydrated electrons (e$_{{\rm aq}}^{-}$) are generated in MSBSL but absent in MBSL. To explore the mechanism of this phenomenon, we numerically simulate the ionization processes in single- and multi-bubble sonoluminescence in aqueous solution of terbium chloride (TbCl$_{3}$). The results show that the maximum degree of ionization of single-bubble sonoluminescence (SBSL) is approximately 10000 times greater than that of MBSL under certain special physical parameters. The hydrated electrons (e$_{{{\rm aq}}}^{-}$) formed in SBSL are far more than those in MBSL provided these electrons are ejected from a bubble into a liquid. Therefore, the quenching of e$_{{{\rm aq}}}^{-}$ to SBSL spectrum is stronger than that of the MBSL spectrum. This may be the reason that the trivalent terbium [Tb(III)] ion line intensities from SBSL in the TbCl$_{3}$ aqueous solutions with the acceptor of e$_{{{\rm aq}}}^{-}$ are stronger than those of TbCl$_{3}$ aqueous solutions without the acceptor of e$_{{{\rm aq}}}^{-}$. Whereas the Tb(III) ion line intensities from MBSL are not variational, which is significant for exploring the mechanism behind the cavitation and sonoluminescence.     

Extreme conditions during multibubble cavitation: Sonoluminescence as a spectroscopic probe

We review recent work on the use of sonoluminescence (SL) to probe spectroscopically the conditions created during cavitation, both in clouds of collapsing bubbles (multibubble sonoluminescence, (MBSL)) and in single bubble events. The effective MBSL temperature can be controlled by the vapor pressure of the liquid or the thermal conductivity of the dissolved gas over a range from ～1600 to ～9000K. The effective pressure during MBSL is ～300bar, based on atomic line shifts. Given nanosecond emission times, this means that cooling rates are >10(12)K/s. In sulfuric and phosphoric acid, the low volatility and high solubility of any sonolysis products make bubble collapse more efficient and evidence for an optically opaque plasma core is found.     

Sonoluminescence: Two sources of light

The model of sonoluminescence with two sources of light is presented. The first of them is gas inside the bubble heated during collapse. The second source (main) is plasma in the breakdown channel in liquid.     

Stable multibubble sonoluminescence bubble patterns

Multibubble standing wave patterns can be generated from a flat piezoceramic transducer element radiating into water. By adding a second transducer positioned at 90 degrees from the transducer generating the standing wave, a 3-dimensional volume of stable single bubbles can be established. Further, the addition of the second transducer stabilizes the bubble pattern so that individual bubbles may be studied. The size of the bubbles and the separation of the standing waves depend on the frequency of operation. Two transducers, operating at frequencies above 500 kHz, provided the most graphic results for the configuration used in this study. At these frequencies stable bubbles exhibit a bright sonoluminescence pattern. Whereas stable SBSL is well-known, stable MBSL has not been previously reported. This paper includes discussions of the acoustic responses, standing wave patterns, and pictorial results of the separation of individual bubble sonoluminescence in a multibubble sonoluminescence environment.     

Sonoluminescence of elementary sulfur melt

The sonoluminescence of liquid sulfur has been observed for temperatures of 120–180°C. The sonoluminescence intensity of the sulfur melt is 10⁹ photons/s at 120°C. As the temperature increases, the luminescence intensity decreases nonmonotonically, a maximum is observed at 160–175°C, and cavitation and luminescence cease at 180°C. The dependence obtained correlates with the temperature dependence of the viscosity of the sulfur melt. The sonoluminescence spectrum obtained with a resolution of 10 nm for 130–150°C contains one band with λ_max = 560 nm, the emitter of which is likely an (S⁺)* ion. When the melt is saturated with argon, the sonoluminescence intensity increases by an order of magnitude; in this case, the spectral band shape changes only slightly. The results confirm the “electric” theory of multibubble sonoluminescence. In the process of the sonolysis of the sulfur melt, biradical fragments are formed in cavitation bubbles consisting of sulfur molecules, which initially have the form of cyclooctasulfur S₈. These fragments can enter into the melts and can be involved in various chemical reactions. This circumstance makes it possible to recommend ultrasonic activation for reactions of sulfurization of hydrocarbons.