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。     

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。     

圆锥气泡声致发光光脉冲和光谱

对一种U形管圆锥气泡发光装置进行了改进，使其发光效果更好，利用光电倍增管和光谱仪 得到了水中空气圆锥气泡的发光脉冲和发光光谱图. 得到的发光脉冲在几百个ps和几个ns之 间不等；在近红外波长范围内观测到了水分子振动能级的特征谱，其连续谱发光强度随着波 长的增加而升高. 另外还得到了在水中加入NaCl溶液的气泡发光光谱图. 关键词： 声致发光 圆锥气泡 光脉冲 光谱     

有机溶液中圆锥泡声致发光

在U形管声致发光装置的基础上建立了一套新型的声致发光装置——直管圆锥泡声致发光装置. 利用此装置以有机溶液为液体介质得到了超强的发光脉冲并测量得到了其发光光谱. 结果表明发光光谱为一从紫外光至可见光波长范围的连续谱,上面叠加有C₂的d³Π_g→d³Π_u跃迁形成的五个序列谱带,分别对应于Δv=-2,Δv=-1,Δv=0,Δv< 关键词： 声致发光 光谱 斯旺带 振动温度     

乙二醇溶液中直管圆锥泡声致发光光脉冲和光谱

在U型管声致发光装置的基础上建立了一套新型的声致发光装置—直管圆锥泡声致发光装置,详细地介绍了此装置的结构和实验操作步骤,利用此装置得到了超强的发光脉冲。测量得到了乙二醇溶液中圆锥泡声致发光的发光脉冲,结果显示脉冲半宽度大约为80 μs左右,远远高于其他声致发光形式所产生的脉冲宽度,这主要是由于圆锥泡可以获得远远高于超声声致发光中气泡所能得到的能量。发光光谱为一从紫外光至可见光波长范围的连续谱,上面叠加C₂有d3Π_g→d3Π_u的跃迁形成的五个序列谱带,分别对应于Δν＝-2,Δν＝-1,Δν＝0,Δν＝1和Δν＝2;同时叠加有CN的B2Σ+→X 2Σ+跃迁形成的3个序列谱带和CH的A2Δ→X 2Π 跃迁谱带。特别是实验中测量得到了斯旺带光谱序列谱带清晰的振动结构。最后,通过与理论模拟得到的斯旺带光谱相对强度的比较,估算得到了C₂分子的振动温度大约为(4 200±200) K。     

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。     

测量单泡声致发光中气泡R(t)曲线的前向Mie散射技术

光干涉原理和Mie理论计算结果表明,单泡声致发光中气泡前向Mie散射的振荡信号,主要是由于气泡的透射光束和表面反射光束之间光干涉产生的. 这些干涉波峰形成了测量气泡半径的空间标尺,标尺的单位长度δR由散射角θ,检测光波波长和流体光折射率确定,而每个波峰就是标尺的刻线,它们与该时刻的气泡半径大小一一对应. 在30°—50°散射角范围内,利用前向Mie散射实验测定了单泡声致发光中气泡的最大半径,R(t)曲线及平衡半径,表明前向Mie散射是一种便捷的测定气泡运动特性的有效方法. 关键词： 单泡声致发光 前向Mie散射 光干涉     

单泡声致发光过程的等离子体描述

对单泡声致发光过程采用等离子体描述,考虑了各种等离子体输运过程,假设了声致发光的轫致辐射机制,数值模拟的结果与实验很好地吻合,有力地支持了声致发光的热转向的解释,预言了声致发光中可能出现的极端电现象,对各物理量时空剖面的分析表明,强电场的出现中能产生的Ｒａｙｌｅｉｇｈ－Ｔａｙｌｏｒ不稳定性有制约作用,这可能是声致发光约１０＾１２能量汇集的原因之一。     

测量单泡声致发光中气泡R(t)曲线的前向Mie散射技术

光干涉原理和Mie理论计算结果表明,单泡声致发光中气泡前向Mie散射的振荡信号,主要是由于气泡的透射光束和表面反射光束之间光干涉产生的.这些干涉波峰形成了测量气泡半径的空间标尺,标尺的单位长度δR由散射角θ,检测光波波长和流体光折射率确定,而每个波峰就是标尺的刻线,它们与该时刻的气泡半径大小一一对应.在30°-50°散射角范围内,利用前向Mie散射实验测定了单泡声致发光中气泡的最大半径,R(t)曲线及平衡半径,表明前向Mie散射是一种便捷的测定气泡运动特性的有效方法.     

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.     

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.     

A correlation between cavitation bubble temperature,sonoluminescence and interfacial chemistry – A minireview

Ultrasound induced cavitation (acoustic cavitation) process is found useful in various applications. Scientists from various disciplines have been exploring the fundamental aspects of acoustic cavitation processes over several decades. It is well documented that extreme localised temperature and pressure conditions are generated when a cavitation bubble collapses. Several experimental techniques have also been developed to estimate cavitation bubble temperatures. Depending upon specific experimental conditions, light emission from cavitation bubbles is observed, referred to as sonoluminescence. Sonoluminescence studies have been used to develop a fundamental understanding of cavitation processes in single and multibubble systems. This minireview aims to provide some highlights on the development of basic understandings of acoustic cavitation processes using cavitation bubble temperature, sonoluminescence and interfacial chemistry over the past 2–3 decades.     

Production of large size single transient cavitation bubbles with tube arrest method

Large size single transient cavitation bubbles of maximum diameter up to 3 cm with sonoluminescence have been generated in water by the ‘tube arrest' method. A simplified one-dimensional model of bubble growing and water column motion is proposed. The results of numerical simulation are compared with the experimental data of the bubble size and oscillation period as the key parameters.     

Conical bubble photoluminescence from rhodamine 6G in 1, 2-propanediol

A modified U-tube conical bubble sonoluminescence device is used to study the conical bubble photoluminescence. The spectra of conical bubble sonoluminescence at different concentrations of rhodamine 6G (Rh6G) solution in 1,2-propanediol have been measured. Results show that the sonoluminescence from the conical bubbles can directly excite Rh6G, which in turn can fluoresce. The light emission of this kind is referred to as conical bubble photoluminescence. The maximum of fluorescence spectral line intensity in the conical bubble photoluminescence has a red shift in relative to that of the standard photo-excited fluorescence, which is due to the higher self-absorption of Rh6G, and the spectral line of conical bubble photoluminescence is broadened in width compared with that of photo-excited fluorescence.     

Sonoluminescence

The results of our studies of sonoluminescence are summarized. Sonoluminescence spectra are interpreted in terms of the distribution of spectral intensity with wavelength, the spectral changes that occur due to scavenging of radiative species, and the shift and the broadening of emission bands. Estimates of conditions within a bubble during collapse are obtained from the spectral features. There is considerable evidence that sonoluminescence is produced by chemical processes induced by thermal mechanism.     

Measurement of pressure and density inside a single sonoluminescing bubble

The average pressure inside a sonoluminescing bubble in sulfuric acid has been determined by two independent techniques: (1) plasma diagnostics applied to Ar atom emission lines, and (2) light scattering measurements of bubble radius vs time. For dimly luminescing bubbles, both methods yield intracavity pressures approximately 1500 bar. Upon stronger acoustic driving of the bubble, the sonoluminescence intensity increases 10,000-fold, spectral lines are no longer resolved, and radius vs time measurements yield internal pressures > 3700 bar. Implications for a hot inner core are discussed.     

Emission from electronically excited metal atoms during single-bubble Sonoluminescence

Variations in sonoluminescence (SL) from an acoustically driven but rapidly translating bubble in solutions of sulfuric acid with alkali-metal salts coincide with variations in translational bubble dynamics. At low acoustic pressures, emission from Ar excited states is observed and the bubble motion is smooth and elliptical. At elevated acoustic pressures, SL intensity decreases, emission from excited alkali-metal atoms is observed, and the bubble motion becomes increasingly erratic with frequent and abrupt changes in direction. These results provide a direct experimental link between single and multibubble SL and point toward the origins of sonochemical reactivity of nonvolatile species.