用SAXS和XRD方法研究TiO2纳米颗粒微观结构

用溶胶-凝胶方法制备了TiO₂纳米样品,并对该样品在300℃到800℃温度区域进行了退火处理.应用同步辐射X射线粉末衍射(XRD)方法研究了经不同热处理温度的TiO₂纳米颗粒的结构相变.应用同步辐射小角X射线散射(SAXS)方法研究了TiO₂纳米颗粒的表面分形与界面特性.得到纳米颗粒粒度与退火温度的变化规律,讨论了表面界面特征与相变的关系. 关键词： X射线小角散射 X射线衍射 2纳米颗粒')" href="#">TiO₂纳米颗粒     

石墨表面熔融硅的润湿行为研究

熔融硅在石墨表面的润湿规律对于超薄硅片的横向拉模制造尤为重要.本文利用COMSOL软件模拟了理想条件下熔融硅在光滑石墨表面的润湿过程,并借助高温高真空接触角测量仪对高温条件下石墨表面熔融硅的润湿性能开展了实验研究.考察了石墨表面粗糙度(R_a=0.721μm与R_a=0.134μm)、环境温度(1737—1744 K)、恒温持续时间(10—30 s)等因素对润湿角的影响.结合固-液、气-液界面的压力、速度分布图,分析了恒定温度、毛细效应下表面张力变化对润湿过程的影响机制.研究结果表明,相同温度下,石墨表面硅液滴的润湿角随石墨表面粗糙度增大而减小.对同一粗糙度表面,润湿角在相同温度下随保温时间的增加略微减小,且变化的幅度随温度升高而减小.当液滴半径远小于5 mm时,表面张力在润湿过程中起主导作用;当液滴半径大于5 mm时,液滴自身重力的影响不可忽略.     

界面极化注极聚丙烯薄膜驻极体的电荷存储特性研究

本文报道一种基于双层介质界面极化机理的新型驻极体注极技术: 借助辅助层对PP薄膜进行注极. 采用表面电位测试方法考察了注极温度、注极电压对所获PP薄膜驻极体电荷存储性能的影响, 并利用热刺激放电技术研究了其高温电荷存储性能, 同时测试了PP薄膜驻极体在X和Y方向的静电场分布. 结果表明: 界面极化注极是一种比电晕注极更为优异的驻极体形成方法. 在一定温度下, 驻极体表面电位随注极电压的增加而增加, 而且两者呈线性关系, 这一结果与注极过程的电荷积聚方程的分析完全一致. 注极温度的影响研究表明, 在保持注极电压不变(注极电压范围为0.5–3.0 kV)的情况下, 温度低于75 ℃时, 温度的变化对于注极效果的影响不明显; 当注极温度大于75 ℃ 时, PP薄膜驻极体的表面电位随注极温度的增加而增加. 表面电位随时间的变化研究表明, PP薄膜驻极体具有良好的电荷存储稳定性. 对其表面电位分布的测试表明, 界面极化注极所形成的PP薄膜驻极体呈现均匀的静电场分布.     

用SAXS和XRD方法研究Ti02纳米颗粒微观结构

用溶胶一凝胶方法制备了TiO2纳米样品.并对该样品在300℃到800℃温度区域进行了退火处理.应用同步辐射x射线粉未衍射(XRD)方法研究了经不同热处理温度的TiO2纳米颗粒的结构相变.应用同步辐射小角x射线散射(SAXS)方法研究了TiO2纳米颗粒的表面分形与界面特性.得到纳米颗粒粒度与退火温度的变化规律,讨论r表面界面特征与相变的关系.     

微颗粒X射线荧光强度MCNPX模拟与WDXRF实验

为研究样品微颗粒在X射线荧光(XRF)分析中对测量结果的影响,运用蒙特卡罗模型MCNPX对X射线荧光仪进行建模,研究了样品颗粒粒径对X射线荧光特征峰强度、峰总比和源峰探测效率的影响,并设计波长色散X射线荧光光谱法(WDXRF)分析实验对模拟结果进行了检验。结果表明：对于样品微颗粒X射线荧光强度与粒径尺寸的关系,MCNPX模拟值与理论计算值保持一致;MCNPX模拟结果与WDXRF实验结果存在一定差异,这取决于MCNPX模型对待测样品状态的假设与实际情况存在一定的差异性;运用样品粉碎、研磨至小颗粒并进行压片处理的办法,可使WDXRF实测结果尽可能的减小与MCNPX理论模拟结果的差异性;在待测样品的颗粒粒径达到一定尺寸时,其峰总比、源峰探测效率、特征峰X射线荧光计数均趋于稳定值;颗粒粒径在某一特定尺寸范围之内,颗粒度效应的影响不容忽视;除此之外,颗粒度效应的影响基本可以忽略。论文充分考虑了待测样品颗粒粒径对XRF分析结果的影响,为减小因颗粒度效应引起分析结果的不确定性提供了一种可行的研究思路,该方法也可为X射线分析的生产实践提供一定的技术参考。     

表面作用对分离式热管小螺旋管蒸发段两相流动与换热特性的影响

本文应用界面化学理论研究表面作用对分离式热管小螺旋管蒸发段管内流动和换热特性的影响。通过实验及分析,提出通过在一定范围内提高热管工作温度和添加润湿剂以降低水的表面张九提高管内壁的粗糙度以增强液膜的铺展性能。利用这两种方法可以有效地增强小螺旋管内壁面的润湿性能,从而提高管内换热性能．     

NiTi合金薄膜厚度对相变温度影响的X射线光电子能谱分析

采用X射线衍射和X射线光电子能谱实验手段对不同厚度的NiTi薄膜相变温度的变化进行了分析.结果表明在相同衬底温度和退火条件下,3?μm厚度的薄膜晶化温度高于18?μm厚度的薄膜.衬底温度越高,薄膜越易晶化,退火后薄膜奥氏体相转变温度As越低.薄膜的表面有TiO₂氧化层形成,氧化层阻止了Ni原子渗出;膜与基片的界面存在Ti₂O₃和NiO.由于表面和界面氧化层的存在,不同厚度的薄膜内层的厚度也不同,因而薄膜越薄,Ni原子的含量就越高.Ni原子的含量的不同会影响薄膜的相变温度. 关键词： NiTi合金薄膜 X射线衍射 相变 X射线光电子能谱     

稠密颗粒射流撞击壁面颗粒膜表面波纹特征

采用高速摄像仪对稠密颗粒射流撞击有限尺寸壁面的流动过程进行了实验研究,重点研究了颗粒膜及其表面波纹特征,考察了颗粒粒径、射流速度和固含率等因素对颗粒膜形态和表面波纹的影响.研究结果表明,随着颗粒粒径增大,稠密颗粒撞壁流由颗粒膜向散射模式转变.与液体射流撞壁液膜相比,颗粒膜扩展角较大,射流速度对其影响不显著.稠密颗粒射流撞壁颗粒膜表面波纹存在明显的叠加现象,颗粒膜表面波纹频率比液膜大约低一个数量级.颗粒膜表面波纹主要由射流脉动引起,表面波纹频率与射流脉动频率具有相同的数量级.     

SnO2纳米晶体的制备、结构与发光性质

使用软化学方法在碱性溶液中制备出了颗粒尺寸分布均匀的SnO2纳米颗粒,使用透射电子显微镜(TEM)、X射线衍射(XRD)、光致发光谱(PL)和光吸收谱等方法分析与表征了SnO2纳米颗粒的结构和光学性能.实验中通过表面活性剂的加入来控制纳米颗粒的结晶与凝聚.XRD,TEM的结果表明,原始制备出的SnO2纳米颗粒的平均粒径小于4 nm,为完好的晶体状态.纳米颗粒经过400-1000 ℃退火后晶粒尺寸进一步增大.光吸收谱表明,相对于体材料,纳米颗粒的禁带宽度展宽并随颗粒尺寸增大而红移.光致发光谱测试表明,不同温度下退火的SnO2纳米颗粒在350-750 nm有较强的发光,研究表明这是来源于颗粒表面的氧空位缺陷发光.     

基于有限元法的非球形颗粒光学常数反演分析

本文基于有限元方法和K-K关系,使用COMSOL与MATLAB动态交互仿真反演非球形颗粒的光学常数。以飞灰颗粒的光学常数为研究对象,首先验证了有限元方法求解球形颗粒衰减因子的准确性,在此基础上采用有限元方法分别求解了球形颗粒、正八面体形颗粒、表面带有微结构的球形颗粒的辐射特性参数,分析了形状因素对颗粒散射特性的影响规律。使用蒙特卡洛方法获得上述三种形状飞灰颗粒系统的透射率光谱,以此为"实验值"反演了其复折射率并与飞灰颗粒真实值比较,得到了较好的结果。     

Prediction of particle sticking efficiency for fly ash deposition at high temperatures

The tendency of ash particles to stick under high temperatures is dictated by the ash chemistry, particle physical properties, deposit surface properties and furnace operation conditions. A model has been developed in order to predict the particle sticking efficiency for fly ash deposition at high temperatures. The model incorporates the particle properties relevant to the ash chemistry, particle kinetic energy and furnace operation conditions and takes into consideration the partial sticking behaviour and the deposit layer. To test the model, the sticking behaviours of synthetic ash in a drop tube furnace are evaluated and the slagging formation from coal combustion in a down-fired furnace is modelled. Compared with the measurements, the proposed model presents reasonable prediction performance on the particle sticking behaviour and the ash deposition formation. Through a sensitivity analysis, furnace operation conditions (velocity and temperature), contact angle and particle size have been found to be the significant factors in controlling the sticking behaviours for the synthetic ash particles. The ash chemistry and furnace temperature dictate the wetting potential of the ash particles and the melting ability of the deposit surface; particle size and density not only control the particle kinetic energy, but also affect the particle temperature. The furnace velocity condition has been identified as being able to influence the selective deposition behaviour, where the maximum deposition efficiency moves to smaller particles when increasing the gas velocity. In addition, the thermophoresis effect on the arrival rate of the particles reduces with increasing the gas velocity. Further, increasing the melting degree of the deposit layer could greatly enhance the predicted deposition formation, in particular for the high furnace velocity condition.     

Surface-coated fly ash used as filler in biodegradable poly(vinyl alcohol) composite films: Part 1—The modification process

The surfaces of fly ash (FA) particles were modified by surfactant, sodium lauryl sulphate (SLS) and used in fabrication of composite films with polyvinyl alcohol (PVA). Both unmodified fly ash (FA) and modified fly ash (SLS-FA) samples were examined using a range of analytical tools including X-ray fluorescence spectroscopy (XRF), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS). The distribution patterns of SLS-FA particles were shifted to the higher regions compared to FA by adding 1.2-4.2 μm in the ranges between 2 and 25 μm, whereas the modification process reduced the size of the particles over 25 μm due to grinding during the activation process. The increased 1.2-4.2 μm in average can be considered the thickness of the surfactant on the SLS-FA surface. On the oxides based chemical analysis by XRF, the compositions were almost unchanged. SEM and TEM were visualised the irregular sizes morphology mostly spherical of the particles, although it is impossible to capture the images of exactly same particles in modified and unmodified forms. The composite films reinforced with SLS-FA showed 33% higher strength than those of FA filled films. The enhancement of tensile strength attributed from the level of physical bonding between SLS-FA and PVA surfaces.     

Enhanced photo-induced hydrophilicity of the sol-gel-derived ZnO thin films by Na-doping

Na-doped ZnO thin films with different Na/Zn ratio were prepared by sol-gel method. The microstructure, chemical composition, surface morphology, and wettability of the thin films were investigated by X-ray diffraction, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy, and water contact angle apparatus. The relation of wettability and Na/Zn ratio has been studied in detail. The wetting behavior of the thin films can be reversibly switched from hydrophobic to hydrophilic, through alternation of UV illumination and dark storage (or thermal treatment). Photo-induced hydrophilicity of the thin films increases with increasing Na/Zn ratio up to 0.08 and then decreases. The mechanism can be attributed to surface nanostructure and the concentration of Na doping.     

Carbon steel wettability characteristics enhancement for improved enamelling using a 1.2 kW high power diode laser

High-power diode laser (HPDL) surface treatment of a common engineering carbon steel (EN8) was found to effect significant changes to the wettability characteristics of the metal. These modifications have been investigated in terms of the changes in the surface roughness of the steel, the presence of any surface melting, the polar component of the steel surface energy and the relative surface oxygen content of the steel. The morphological and wetting characteristics of the mild steel and the enamel were determined using optical microscopy, scanning electron microscopy (SEM), X-ray photoemission spectroscopy (XPS), energy-dispersive X-ray (EDX) analysis and wetting experiments by the sessile drop technique. This work has shown that HPDL radiation can be used to alter the wetting characteristics of carbon steel so as to facilitate improved enamelling.     

Biomass fly ash deposition in an entrained flow reactor

Fly ash deposition on boiler surfaces is a major operational problem encountered in biomass-fired boilers. Understanding deposit formation, and developing modelling tools, will allow improvements in boiler efficiency and availability. In this study, deposit formation of a model biomass ash species (K₂Si₄O₉) on steel tubes, was investigated in a lab-scale Entrained Flow Reactor. K₂Si₄O₉ was injected into the reactor, to form deposits on an air-cooled probe, simulating deposit formation on superheater tubes in boilers. The influence of flue gas temperature (589 – 968°C), probe surface temperature (300 – 550°C), flue gas velocity (0.7 – 3.5?m/s), fly ash flux (10,000 – 40,000?g/m²h), and probe residence time (up to 60?min) was investigated. The results revealed that increasing flue gas temperature and probe surface temperature increased the sticking probability of the fly ash particles, thereby increasing the rate of deposit formation. However, increasing flue gas velocity resulted in a decrease in the deposit formation rate, due to increased particle rebound. Furthermore, the deposit formation rate increased with probe residence time and fly ash flux. Inertial impaction was the primary mechanism of deposit formation, forming deposits only on the upstream side of the steel tube. A mechanistic model was developed for predicting deposit formation in the reactor. Deposit formation by thermophoresis and inertial impaction was incorporated into the model, and the sticking probability of the ash particles was estimated by accounting for energy dissipation due to particle deformation. The model reasonably predicted the influence of flue gas temperature and fly ash flux on the deposit formation rate.     

ICP-OES分析低钙粉煤灰在NaOH溶液中离子浸出规律

低钙粉煤灰潜在的火山灰活性释放缓慢限制了其大规模利用,通过碱激发提高粉煤灰中Si4+,Al3+和Ca2+等离子浸出率对于加快低钙粉煤灰活性释放具有积极作用。采用电感耦合等离子体发射光谱、傅里叶变换红外光谱、X射线衍射和扫描电子显微镜分别测试和分析了5种浓度NaOH溶液对低钙粉煤灰激发过程中Si4+,Al3+和Ca2+的浸出规律、化学基团变化、水化产物生成及微观形貌演化。结果表明：碱激发作用显著提高了低钙粉煤灰中Si4+,Al3+和Ca2+浸出率,三种离子浸出率大小为：Si4+＞Al3+＞Ca2+,其中Si4+和Al3+浸出率随NaOH浓度增加而增加,随浸出时间延长呈对数规律升高;Ca2+由于在NaOH溶液中生成Ca(OH)₂沉淀,其浸出率大小表现为在水中高,在NaOH溶液中低。红外光谱清晰地表征出低钙粉煤灰受碱激发作用后化学基团在指纹区(波数1 300 cm-1以下)的变化,且随碱激发时间的延长和碱浓度的增加变化愈加明显。水化产物和微观形貌的结果显示出粉煤灰颗粒表面受到碱侵蚀发生解聚,在OH-催化下,硅铝单体分子重新排列形成硅酸盐和铝酸盐低聚络合物,通过亲核取代反应形成铝硅酸盐的低聚态溶胶,并进一步与碱金属阳离子通过配位键或静电键的作用缩聚形成水化凝胶类产物。采用ICP-OES测试粉煤灰中离子浸出率可作为评价粉煤灰火山灰活性的一种快速和准确的方法。     

正癸烷纳米液滴润湿特性的分子动力学研究

流体液滴在固体表面的浸润性对其润滑性能至关重要.本文利用分子动力学方法研究了正癸烷纳米液滴在铜表面上的润湿特性.结果表明：在平坦光滑表面上,壁面的厚度和分子数目对润湿效果影响不大.随着壁面能量势阱参数εs 增大,接触角线性减小.随着温度升高,液滴的接触角减小.在沟槽粗糙表面上,随着粗糙度因子增大,对于疏液表面,接触角增大到一定值后基本保持不变,符合Cassie理论;中性和亲液表面接触角则会减小,为Wenzel润湿模式.当表面分数增大时,疏液与亲液表面接触角整体呈减小的趋势,对中性表面影响不大.当温度升高时,粗糙疏液表面接触角会增大,润湿效果更差,而粗糙中性和亲液表面液滴润湿性会更好.     

Room temperature synthesis of water-repellent polystyrene nanocomposite coating

A stable superhydrophobic polystyrene nanocomposite coating was fabricated by means of a very simple and easy method. The coating was characterized by scanning electron microscopy and X-ray photoelectron spectrum. The wettability of the products was also investigated. By adding the surface-modified SiO₂ nanoparticles, the wettability of the coating changed to water-repellent superhydrophobic, not only for pure water, but also for a wide pH range of corrosive liquids. The influence of the drying temperature and SiO₂ content on the wettability of the nanocomposite coating was also investigated. It was found that both factors had little or no significant effect on the wetting behavior of the coating surface.     

Composite Ni-Co-fly ash coatings on 5083 aluminium alloy

Ni-Co-fly ash coatings were deposited on zincate treated 5083 wrought aluminium alloy substrates with the aid of the electrodeposition technique. Structural and chemical characterization of the produced composite coatings was performed with the aid of X-ray diffraction (XRD), scanning electron microscopy (SEM) and electron dispersive X-ray analysis (EDS) techniques. The Ni-Co-fly ash coatings were found to consist of a crystalline Ni-Co solid solution with dispersed fly ash particles. In addition, chemical analysis of the Ni-Co matrix showed that it consisted of 80 wt.% Ni and 20 wt.% Co. The co-deposition of fly ash particles leads to a significant increase of the microhardness of the coating. The corrosion behaviour of the Ni-Co-fly ash/zincate coated aluminium alloy, in a 0.3 M NaCl solution (pH = 3.5), was studied by means of potentiodynamic corrosion experiments.     

Experimental study on electrostatic removal of high-carbon particle in high temperature coal pyrolysis gas

A high-temperature electrostatic precipitator (ESP) presents a good solution for hot gas cleaning, which can remove fly ash from pyrolysis gas at temperatures higher than the tar dew point. In this paper, the characteristics of negative DC corona discharge in air and simulated coal pyrolysis gas were studied. The removal of coal pyrolysis furnace fly ash (ash A) was investigated and compared with that of coal-fired power plant fly ash (ash B) in ESP with a temperature ranging from 300?K to 900?K. The current density of simulated gas was higher than that of air under the same discharge voltage and at different temperatures. The simulated gas also had a higher spark voltage and a lower onset voltage compared with air. The fractional collection efficiency of ash A was lower for particles with diameters of larger than 0.1?µm at high temperature, compared with ash B. A lower collection efficiency in simulated gas was obtained for particles with diameters of less than 0.1?µm compared with air. The collection efficiency of submicron particles in simulated gas was usually higher than it in air, especially for particles with diameters of less than 0.04?µm. In simulated gas, the overall collection efficiency of ash A was obviously lower than that of ash B, especially at high temperature. From 300?K to 700?K, the collection efficiencies of both ash samples were as high as above 93%, but the collection efficiency of ash A in simulated gas decreased to 78.7% at 900?K.