双低频超声处理偶氮类染料模拟废水的研究

对用双低频超声波处理偶氮染料活性艳红X-3B模拟废水进行了实验研究。探讨了不同超声波之间的功率搭配和超声波探头之间的距离对处理效果的影响。实验表明双频超声降解效果优于单频超声，双频超声存在最佳功率搭配。在给定的实验范围内，两个超声波探头之间的最佳距离为1．5cm，US／Fenton处理污染物的效果（η值为94．90％）高于US与Fenton处理效果之和7．1个百分点。通过UV-Vis分析，观察到活性艳红X-3B处理60min后基本被矿化。     

超声波降解有机物溶液的气泡动力学研究

在超声波降解有机物溶液过程中,超声空化产生的高温高压以及空化泡振荡产生的激波在有机物溶液的降解中发挥重要作用.本文通过对超声波作用下气泡动力学的研究,讨论了超声波声压、频率、气泡初始半径等参量对有机物溶液降解效率的影响.研究发现.存在使降解效率极大的声压和频率.在空化稳定的情况下,存在一个使降解效率极大的气泡初始半径,降解效率随着黏滞系数的增大而减小.研究还发现,双频超声作用的空化效果比单频超声作用时强,与双频超声作用下有机物溶液降解率较大这一实验结果一致.     

160kHz超声协同臭氧蔬果药残降解仪的设计与乙酰甲胺磷降解实验*

针对现有超声协同臭氧降解农药的研究多集中在20kHz至50kHz的频段内,而效果一直不够理想,以及目前民用的超声协同臭氧蔬果药残降解装置较少的问题,设计了一种160kHz超声协同臭氧蔬果药残降解仪。超声波发生器采用SG3525芯片驱动半桥式功率放大电路,并运用小范围扫频技术。臭氧发生器使用市场上量产的小型臭氧机。本文利用该降解仪进行了乙酰甲胺磷农药降解实验,对160kHz超声波协同臭氧的农药降解效果进行了初步研究,结果表明仪器对降解乙酰甲胺磷有效。     

PEG6000溶液超声化学反应机理的初步研究

采用不同电功率的超声波处理了聚乙二醇(PEG6000)溶液。凝胶渗透色谱(GPC)分析超声处理后的PEG溶液发现,当超声电功率超过250W时,PEG分子量随超声波作用强度的增大而减少,随超声波作用时间的延长而增大;在电功率超过250W超声波作用下,傅立叶红外光谱(FT-IR)分析表明,组成PEG的单体没有明显改变,但是,羟基含量分析表明,PEG固体样品中的羟基含量有所减少。结合实验结果,根据高分子化学、有机化学和超声化学中相关理论对PEG超声化学反应机理进行了探讨,认为:当超声波作用于PEG溶液时,同时存在有PEG的缩水聚合反应和自由基降解反应,当频率为20-25kHz、电功率为250-600W的超声作用于PEG6000溶液时,缩水聚合反应占主导地位。     

超声波与电化学协同作用降解硝基苯溶液的实验研究

本文以硝基苯模拟废水为研究对象，探讨了超声波与电化学协同作用降解硝基苯的实验情况。考察了处理时间、处理温度、硝基苯初始浓度、pH值、电解电压等因素对硝基苯降解率的影响。实验结果表明：随着作用时间增加，硝基苯的降解率升高；温度高于40℃时，硝基苯的降解率随温度的升高而降低，低于40℃时，硝基苯的降解率随温度的升高而增大；硝基苯的降解率随电压的升高而增大；酸性条件有利于硝基苯的降解；硝基苯初始浓度越大降解率越高。     

超声波降解溴苯:操作参数与环境因素的影响

本文考察了用超声波降解水中溴苯的动力学与脱卤效应,并研究了重要的操作参数如强度与饱和气体,以及环境干扰因素如悬浮物、地表水其他杂质的影响。结果表明,超声波可以有效地处理溴苯,在20kHz,7.5W／cm2下一级反应常数达0.044／min,脱卤效率达58％。本研究范围内,声强度越高,反应越快。氧气和氩气下降解速率高于空气下。超声降解不受地表水中杂质、纳米级微粒、无机颗粒的影响,但有机悬浮物能在一定程度上干扰溴苯的超声降解。     

快速制取人体组织病理切片的超声波法

本文介绍了用超声波方法快速制妈人体组织病理切片的基本原理，实验步骤和试验结果。结果表明，用超声波处理后快速制取的病理切片完全怀可常规石蜡切片相媲美，在临床外检快速病理诊断应用上，超声处理仪有可能取代价格昂贵的恒温式冷冻切片机。     

超声空化状态对苯酚降解的影晌

给出不同空化状态下超声波降解苯酚溶液的实验结果,比较了相应的声压级频谱和合成声强。研究了苯酚溶液的浓度、二阶铁盐、超声辐照时间对苯酚降解率的影响,讨论了不同空化状态下的声压级频谱特征。     

超声空化状态对苯酚降解的影响

给出不同空化状态下超声波降解苯酚溶液的实验结果,比较了相应的声压级频谱和合成声强。研究了苯酚溶液的浓度,二阶铁盐,超声辐射时间对苯酚降解率的影响,讨论了不同空化状态下的声压级频谱特征。     

超声波与光协同降解对氯苯酚水溶液的机理研究

为阐明超声波与光协同作用机理,以对氯苯酚为研究对象,研究了对氯苯酚水溶液在超声波与光(紫外光,可见光)单独及共同辐照下的降解现象,研究发现对氯苯酚水溶液在超声波及紫外光单独辐照下均发牛降解,降解过程符合一级反应动力学规律.在超声波和紫外光共同辐照下,降解过程也符合一级反应动力学规律,同时对氯苯酚水溶液降解呈现显著的声光协同效应,即同一辐照时间内超声波和紫外光共同辐照下对氯苯酚的降解率大于超声波和紫外光单独辐照下各自降解率之和.另一方面,超声波和可见光共同辐照没有呈现出明显的卢光协同效应.超声波和紫外光共同辐照下的声光协同效应被归因于紫外光对超声空化过程中产生的过氧化氢的裂解作用.     

Mechanochemical degradation kinetics of high-density polyethylene melt and its mechanism in the presence of ultrasonic irradiation

In this paper, the effect of ultrasonic intensity on the degradation of high-density polyethylene (HDPE) melt, degradation mechanism, ultrasonic degradation kinetics of HDPE melt as well as the development of molecular weight distribution of HDPE melt during ultrasonic degradation were studied. In the initial stage, the ultrasonic degradation of HDPE melt shows a random scission process, and the molecular weight distribution broadens. After that, the ultrasonic degradation of HDPE melt shows a nonrandom scission process, and the molecular weight distribution of HDPE melt narrows with ultrasonic irradiation time. The average molecular weight of HDPE decreases with the increase of ultrasonic intensity and increases and trends forward that of undegraded HDPE with the increase of distance from ultrasonic probe tip, indicating that attenuation of ultrasonic intensity in HDPE melt is very quick. Ultrasonic degradation kinetics of HDPE melt obeys the equation: Mt=M(infinity) + Ae(-kt). The theoretic calculation by this equation accords well with the experimental results. The plausible ultrasonic degradation mechanism of polymer melt based on molecular relaxation was also proposed in this paper.     

Effect of various sono-oxidation parameters on the removal of aqueous 2,4-dinitrophenol

The influences of ultrasonic output intensity, solution pH, H₂O₂ concentration and the addition of Fenton reagent on the degradation of 2,4-dinitrophenol (DNP) under ultrasonic irradiation were investigated. It was observed that the degradation of DNP fitted pseudo-first-order dynamics under our experimental conditions. Increasing the ultrasonic output intensity increased the degradation efficiency of DNP and low pH favored the ultrasonic degradation of DNP. The addition of H₂O₂ enhanced the ultrasonic degradation efficiency of DNP. The further addition of Cu²⁺, however, hindered the degradation of DNP. In contrast, sono-oxidation treatment in combination with FeSO₄/H₂O₂ showed a synergistic effect for DNP degradation.     

温度对潜望式激光通信终端SiC反射镜性能影响

分析了温度梯度和均匀温度对潜望式激光通信终端反射镜形变的影响,利用椭圆域上的Zerni-ke多项式对椭圆反射镜的波前进行拟合,计算由于热形变导致的波前畸变误差,给出了星间激光通信终端反射镜均方根值、发射光束瞄准误差、接收端光强随温度梯度和均匀温度的变化关系。结果表明:温度梯度对反射镜的影响只是引起峰值光强的漂移和少许下降,当温度梯度为14℃/m时瞄准误差达2.1μrad。均匀温度会引起接收端的光强分布变化,从而导致很大的瞄准误差和光强衰减,当均匀温度与参考温度的差值小于0.6℃时,由波前畸变误差引起的瞄准误差小于1μrad,当差值大于0.6℃时,瞄准误差突然增大到几μrad,接收端光强分布发生变化,此时反射镜热形变引起的像散项对光强分布起重要作用。     

Polymer electrolyte fuel cell performance degradation at different synchrotron beam intensities

The degradation of cell performance of polymer electrolyte fuel cells under monochromatic X‐ray irradiation at 13.5 keV was studied in galvanostatic and potentiostatic operation modes in a through‐plane imaging direction over a range of two orders of magnitude beam intensity at the TOMCAT beamline of the Swiss Light Source. The performance degradation was found to be a function of X‐ray dose and independent of beam intensity, whereas the degradation rate correlates with beam intensity. The cell performance was more sensitive to X‐ray irradiation at higher temperature and gas feed humidity. High‐frequency resistance measurements and the analysis of product water allow conclusions to be drawn on the dominating degradation processes, namely change of hydrophobicity of the electrode and sulfate contamination of the electrocatalyst.     

老化产生的深能级对GaP纯绿发光二极管发光效率的影响

测量了GaP纯绿发光二极管老化前后的可见和近红外发光光谱,研究了老化产生的深能级的来源及其对二极管发光效率的影响.在老化后的发光光谱中观测到650nm和1260nm发光带,发现1260nm发光带的发光强度随老化时间的增加而增强.实验结果表明老化产生的与磷相关的深能级严重地影响了GaP纯绿LED的发光效率.     

激光光强扰动对相干场成像降质影响理论研究

激光相干场成像系统发射多束激光,经大气传输对远程目标成像,大气湍流引起的激光束光强扰动是影响成像质量的一个关键因素.本文从湍流引起的激光束光强扰动对回波解调信号的影响关系入手,建立了激光回波光强扰动因子对相位闭合系数和成像频谱分量的降质传函理论模型;基于三光束激光相干场成像系统仿真验证了理论模型的有效性.研究表明激光相干场成像频谱分量和成像像质主要受三光束相位闭合求解算法中第二光束光强扰动影响.该研究揭示了激光回波光强扰动对成像像质的影响机理,对于分析大气湍流等引起的光强扰动降质效应和合理分配多光束光强稳定性以提高成像质量具有理论指导意义.     

Ultrasonic degradation of butadiene, styrene and their copolymers

Ultrasonic degradation of commercially important polymers, styrene-butadiene (SBR) rubber, acrylonitrile-butadiene (NBR) rubber, styrene-acrylonitrile (SAN), polybutadiene rubber and polystyrene were investigated. The molecular weight distributions were measured using gel permeation chromatography (GPC). A model based on continuous distribution kinetics approach was used to study the time evolution of molecular weight distribution for these polymers during degradation. The effect of solvent properties and ultrasound intensity on the degradation of SBR rubber was investigated using different pure solvents and mixed solvents of varying volatility and different ultrasonic intensities.     

Degradation of Y2SiO5:Ce phosphor powders

The degradation of the cathodoluminescence (CL) intensity of cerium-doped yttrium silicate (Y₂SiO₅:Ce) phosphor powders was investigated for possible application in low voltage field emission displays (FEDs). Auger electron spectroscopy (AES), X-ray photoelectron spectroscopy (XPS) and CL spectroscopy were used to monitor changes in the surface chemical composition and luminous efficiency of commercially available Y₂SiO₅:Ce phosphor powders. The degradation of the CL intensity for the powders is consistent with a well-known electron-stimulated surface chemical reaction (ESSCR) model. It was shown with XPS and CL that the electron stimulated reaction led to the formation of a luminescent silicon dioxide (SiO₂) layer on the surface of the Y₂SiO₅:Ce phosphor powder. XPS also indicated that the Ce concentration in the surface layer increased during the degradation process and the formation of CeO₂ and CeH₃ were also part of the degradation process. The CL intensity first decreased until about 300 C cm⁻² and then increased due to an extra peak arising at a wavelength of 650 nm.     

Ultrasound enhanced degradation of Rhodamine B: optimization with power density.

Degradation of Rhodamine B, a waste water dye effluent was studied under the influence of ultrasound. In the present study, optimization of this degradation was carried out with power parameters, namely, power density (W/ml) and power intensity (W/cm2) using different ultrasonic equipments. From the studies, it has been observed that the degradation does not increase indefinitely with an increase in the power parameters, but instead, it reaches an optimum value and then decreases with a further increase in the power parameters. Also, these optima were not the same in all the ultrasonic equipments in which these studies were carried out. Difference in the type of acoustic field generated may be responsible for the different power optima observed with different ultrasonic equipments. The comparative study of the degradation of Rhodamine B using various ultrasonic equipments establishes a relationship between the area-specific parameter (intensity) and the volume-specific parameter (density) of reactivity.     

Study on degradation of dimethoate solution in ultrasonic airlift loop reactor

In this work, the degradation of dimethoate solution in ultrasonic airlift loop reactor (UALR) assisted with advanced oxidation processes was studied. The effects of O₃ flow rate, ultrasonic intensity, pH value and reaction temperature on the degradation rate were investigated. UALR imposed a synergistic effect combining sonochemical merit with high O₃ transfer rate. Under the optimal operation conditions: ultrasonic irradiation time was 4 h, O₃ flow rate was 0.41 m³ h⁻¹, ultrasonic intensity was 4.64 W cm⁻², pH value was 10.0, reaction temperature was 25 °C, and initial concentration of dimethoate was 20 mg L⁻¹, degradation rate of dimethoate increased to 90.8%. The experimental results indicated that the method of UALR degradation of organic pollutants in the presence of gas could reduce reaction time and improve degradation rate. UALR was an advisable choice for treating organic waste waters and this device could be easily scale up. Thus this process has wide application prospect in industry.