采用改进的曳力模型模拟2D鼓泡流化床的流化特性

针对特定颗粒浓度范围颗粒团聚作用导致的曳力下降问题,基于传统曳力模型在不同颗粒浓度段的特性分析,选择适用于不同颗粒浓度区间的曳力模型,通过光滑函数得到改进的曳力模型,并耦合欧拉双流体模型对2D鼓泡流化床进行数值模拟. 结果表明,与Gidaspow和Syamlal-O'Brien模型相比,改进的曳力模型对床层局部压降的预测结果更好;随表观气速增加,改进的曳力模型能更准确地预测床层膨胀;当表观气速Ug=0.46 m/s时,改进的曳力模型对径向颗粒浓度分布的模拟结果明显好于Syamlal-O'Brien模型.     

错列双管涡激振动风洞实验研究

针对横向流作用下换热器管束的涡激振动问题,采用低速回流式风洞对错列双管结构的涡激振动特性进行了实验研究,测量并分析了横向流作用下雷诺数和节径比对双圆管结构涡激振动特性的影响。实验中错列双管结构的水平距L/D范围为1. 5～3. 0,错位距H/D范围为0. 00～0. 75,风速U范围为0～18m/s。实验结果表明:在实验流速范围内,结构振幅先随流速的增加缓慢变化,流速达到临界值时振幅会突变增大,进入锁频区域,出现涡激共振现象。错列双管结构随水平距的增加,上游管尾流干扰对下游管柱的影响减弱。错位距较小时,下游管临界流速更小,锁频区间更宽。     

基于格子Boltzmann方法的单颗粒绕流数值模拟

采用格子Boltzmann方法（LBM）研究了单颗粒绕流流动过程。通过使用LBM中的LBGK（lattice Bhatnagar-Gross-Krook）模型和二阶精度的曲线边界条件处理方法,实现了对单颗粒绕流问题的定常及非定常流动过程中涡结构的模拟。采用动量交换法分别计算了Reynolds数在0.1～200范围内27个不同Reynolds数时的曳力系数,并将计算结果拟合得到基于LBM数值模拟的曳力曲线。计算结果表明,LBM在气固两相流的模拟计算中具有精确、可靠的优点,使用LBM模拟计算曳力曲线的方法经济、易行,并且可以克服由传统实验方法获得曳力曲线的局限性。     

基于EMMS介尺度模型的双分散鼓泡流化床的模拟

双分散气固鼓泡流化床中颗粒通常具有不同粒径或密度,导致产生颗粒偏析等现象,影响传递和反应行为。颗粒分离和混合与气泡运动密不可分,其中相间曳力起关键作用。最近Ahmad等提出了一种基于气泡结构的双分散介尺度曳力模型,能成功预测双分散鼓泡流化床的床层膨胀系数。本研究耦合该曳力模型与连续介质方法,模拟了两种不同的双分散鼓泡流化床,通过分析不同流化状态下的气泡运动、颗粒浓度比的轴向分布等参数,进一步检验模型的适用性。研究表明,当双分散颗粒处于完全流化状态时,耦合双分散介尺度曳力模型可合理预测不同颗粒的分离现象;而其处于过渡流化状态时,新曳力模型和传统模型均无法获得合理结果,此时调节固固曳力可改进模拟结果。     

基于EMMS介尺度模型的双分散鼓泡流化床的模拟

双分散气固鼓泡流化床中颗粒通常具有不同粒径或密度,导致产生颗粒偏析等现象,影响传递和反应行为。颗粒分离和混合与气泡运动密不可分,其中相间曳力起关键作用。最近Ahmad等提出了一种基于气泡结构的双分散介尺度曳力模型,能成功预测双分散鼓泡流化床的床层膨胀系数。本研究耦合该曳力模型与连续介质方法,模拟了两种不同的双分散鼓泡流化床,通过分析不同流化状态下的气泡运动、颗粒浓度比的轴向分布等参数,进一步检验模型的适用性。研究表明,当双分散颗粒处于完全流化状态时,耦合双分散介尺度曳力模型可合理预测不同颗粒的分离现象;而其处于过渡流化状态时,新曳力模型和传统模型均无法获得合理结果,此时调节固固曳力可改进模拟结果。     

垂直气固两相流动体系中气固两相之间的协同效应探讨

垂直气固两相流动体系中,气体与颗粒之间的相互作用在一定的颗粒浓度范围内存在协同效应.这种协同效应的表现形式是颗粒群中每个颗粒的平均曳力系数CD与单颗粒曳力系数CDs之比CD/CDs＜1.0,协同效应的大小可以用准数Sy=1/(CD/CDs)描述.气固两相之间产生协同效应的微观机制是颗粒之间存在着团聚,这种颗粒团聚使气固两相流动消耗的能量降低,此时气固两相之间的动量和能量传递以能量消耗为最小的方式进行.     

循环流化床内颗粒的加速作用及气固两相间的动量交换

根据对气固两相流动特性的分析,表明在循环流化床提升管内,颗粒的加速运动及气固两相间的动量交换对床层各项参数具有明显的影响。由于颗粒聚集,减小了气固两相间的相互作用,使曳力系数小于单颗粒标准曳力系数(C_D/C_(DS)<1.0)。从而使颗粒具有较长的加速段,其加速压降在总压降中所占的分率不可忽略。考虑颗粒加速作用及由于颗粒聚集使气固两相相互作用力减小的事实后,用一维轴向稳态流动的模型可以获得截面平均空隙率、平均颗粒速度以及曳力系数等参数及其轴向分布规律,并与实验直接测定结果吻合很好。通过对大量数据的分析,表明C_D/C_(DS)可用下述经验关联式表示:C_D/C_(DS)=1.68(ε)~(0.253)(Re_(?)/Re_t)~(-1.213)(d_P/D)~(0.105)     

液滴降落过程表面曳力及其形状改变规律

在单颗粒液滴-气流体系中,采用计算流体力学方法对速度发展段的输运现象进行数值模拟。研究液滴在气流中逆流运动的形态变化规律与局部传递特征。获得在30相似文献   

射流卷吸边界层内相干结构的实验研究

在轴对称水射流实验台上,采用单帧长曝光图像法,测量了出口Reynolds数在1849～2509范围内的卷吸边界层内流场结构。发现在流向距离L=2D～3.5D,径向距离H=D～1.25D的区域内,流场中吞噬作用和侵蚀作用两种卷吸模式交替出现。分析得到,当Re1915时,吞噬作用所占的比例随着Re的增大而增大,当Re2311之后,Reynolds数对该结构发生概率的影响降低;通过快速傅里叶变换得到该相干结构发生的频率在10～19Hz之间;吞噬作用发生的同时在流场中观测到一些特殊涡结构。同时采用运动单帧长曝光图像法对射流流场进行拉格朗日法观测,发现射流流场中的涡结构一般存在于湍流与非湍流界面附近。     

颗粒团绕流曳力系数的LBM计算

采用格子Boltzmann方法(Lattice Boltzmann method, LBM) 中的LBGK(Lattice Bhatnagar- Gross-Krook)模型和二阶精度的曲线边界条件处理方法对二维颗粒团绕流现象进行了数值模拟,并同时使用动量交换法计算了两种颗粒团构型中不同颗粒的曳力系数。结果表明：颗粒团曳力系数与颗粒聚团的构型有着密切联系,颗粒聚团的形成将导致颗粒团曳力系数大幅度减小。除颗粒团构型因素外,颗粒间距和流动Reynolds数也是导致颗粒团曳力系数发生改变的主要因素。当颗粒聚团存在时,颗粒团中不同颗粒的受力有较大差异,若忽略颗粒聚团效应,则颗粒团曳力系数的计算必然将产生偏差。     

Surface dynamics during latex film formation

Surface dynamics during latex film formation has been investigated theoretically and experimentally by atomic force microscopy. The peak-to-valley distance, y(t), of the latex particles in the surface plane of the latex film decayed exponentially with time during film formation. A theoretical relationship between y(t) and time, t, is given by y(t)=y(0) exp[−t/τ], where y(0) is the value of y(t) when t is zero. τ is a characteristic constant related to the nature of polymer, the particle radius, the surface diffusion coefficient and the temperature. The relationship between the surface diffusion coefficient, D_s, y(0), the radius of the latex particles, R, temperature, T, and τ is given approximately by D_s=1.2×10⁻²⁰y(0)²[2R−y(0)]²T/τ (cm²/s), where the units are manometers for y(0) and R, kelvin for temperature, and seconds for τ. By measuring the decay of y(t) with time, the surface diffusion coefficient can be obtained. The surface diffusion coefficient for a poly(methyl methacrylate-co-butylacrylate) (50:50) copolymer latex film was found to be A×10⁻¹³ cm²/s, A is temperature-dependent.     

Gas–liquid mass transfer coefficient in stirred tanks interpreted through models of idealized eddy structure of turbulence in the bubble vicinity

Experimental data on the average mass transfer liquid film coefficient (k_L) in an aerated tank stirred by two Rushton turbines on common shaft are presented. Liquid media used were distilled water and 0.5 M sodium sulphate solution. Volumetric mass transfer coefficient (k_La) was measured by the dynamic pressure method with pure oxygen absorption. Specific interfacial area a was taken from Alves et al. [Chem. Eng. Proc., in press] who measured data on local gas hold-up and local average bubble diameter in the same apparatus and batches. Values of k_L are quantitatively interpreted in terms of correlations based on idealized eddy structures of turbulence in the bubble vicinity, namely by “eddy” model by Lamont and Scott [AIChE J. 16 (1970) 513] in the form of k_L=0.523(eν/ρ)^0.25(D/ν)^1/2, which fits the data with the mean deviation of 4.7%. It is shown that the decisive quantity to correlate k_L in the stirred tank is power dissipated in the liquid phase rather than the bubble diameter and the slip velocity as assumed by Alves et al.     

舒巴坦钠溶析结晶工艺优化

目前舒巴坦钠粗品的提纯采用还原成舒巴坦酸后再经反应结晶合成舒巴坦钠的方式，耗时耗力且所需药品、试剂种类较多，不节能环保。针对该问题，采用正交实验 L_{27} \left(3^{13}\right) 对舒巴坦钠的溶析结晶工艺进行优化，探明了6个因素6个交互作用对粒度、纯度以及两者的综合评分的影响，包括养晶时间（A）、溶析剂用量（B）、溶析剂中乙醇的体积分数（C）、溶析剂的滴加速率（D）、搅拌速率（E）、温度（F）以及养晶时间分别与溶析剂用量（A×B）、与溶析剂中乙醇的体积分数（A×C）的交互作用、溶析剂用量与溶析剂中乙醇的体积分数的交互作用（B×C），并得到了一组最优方案A ₂ B ₂ C ₁ D ₃ E ₃ F ₂。通过该方案可获得纯度x>97%，体积平均粒度D[4,3]≈290μm，质量收率约为84%的舒巴坦钠产品，并发现杂质舒巴坦青霉胺对舒巴坦钠的粒度分布有一定的影响。在解决原有问题的基础上，合适粒度分布的舒巴坦钠产品也可为后续制剂工艺提供方便。     

Mass transfer in liquid films during absorption part I. Comparison of mass transfer models with experiments

Experimental values of the liquid-side mass transfer coefficient k_L for absorption of gases of low solubility in a liquid film flowing down a smooth and a rough wetted wall and down an expanded metal sheet are compared with selected mass transfer models. It is shown that the set of published k_L values available is insufficient to evaluate the most suitable model with which to describe the mass transfer mechanism. One of the distinguishing features of the various mass transfer models is the value of exponent m in the dependence of k_L on molecular diffusivity, k_L D^m. The range of published experimental values is 0.5 < m < 0.7; nevertheless, these results are insufficient for this purpose as well. It is shown that experimental determination of exponent m in the range of high Schmidt numbers could give new information about the phenomena very near the gas—liquid interface which is of importance when discussing the mass transfer mechanism in a liquid film during absorption. In discussing different models in this work special attention is given to the recently published film-penetration model proposed to evaluate k_L for absorption into a liquid film on an expanded metal sheet.     

Dilute solution properties of carboxymethylchitins in high ionic-strength solvent

The hydrodynamic characteristics in aqueous solution at ionic strength I=0.2  of carboxymethylchitins of different degrees of chemical substitution have been determined. Experimental values varied over the following ranges: the translational diffusion coefficient (at 25.0°C), 1.1<10⁷×D<2.9 cm² s⁻¹; the sedimentation coefficient, 2.4<s<5.0 S; the Gralen coefficient (sedimentation concentration-dependence parameter), 130<k_s<680 mL g⁻¹; the intrinsic viscosity, 130<[η]<550 mL g⁻¹. Combination of s with D using the Svedberg equation yielded ‘sedimentation–diffusion' molecular weights in the range 40 000<M<240 000 g mol⁻¹. The corresponding Mark–Houwink–Kuhn–Sakurada (MHKS) relationships between the molecular weight and s, D and [η] were: [η]=5.58×10⁻³ M^0.94; D=1.87×10⁻⁴ M^−0.60; s=4.10×10⁻¹⁵ M^0.39. The equilibrium rigidity and hydrodynamic diameter of the carboxymethylchitin polymer chain is also investigated on the basis of wormlike coil theory without excluded volume effects. The significance of the Gralen k_s values for these substances is discussed.     

三角槽道低 Reynolds 数脉动流与柔性壁耦合特性研究

以水为工质对三角槽道低 Reynolds 数脉动流与柔性壁耦合特性进行了实验研究。通过传热与流动实验,分析了脉动频率(W)、脉动振幅(A)、柔性壁特性对脉动流传热及流动的影响。同时,通过可视化实验,研究了柔性壁与脉动流之间的响应特性,解析了柔性壁形变与振频对脉动流传热及流动的作用机制及分离贡献。研究结果表明,柔性流道脉动流可以实现强化传热与流动减阻双重效果,但强化传热效果相对较弱(传热效率提升0~50%),适用于以减阻为主要目的的换热场合;柔性壁减阻与削弱强化传热效率,源于柔性壁形变造成时均流通截面积增大(流体流速下降)、W与A的增大减弱脉动能量;W的增加将使得柔性壁振动对脉动流强化传热效率的削减逐步趋于主导地位,而A的增加将使得柔性壁变形对脉动流强化传热效率的削减逐步趋于主导地位;脉动流阻力的削减主要来自于柔性壁的变形(D₁>70%),而柔性壁振频对于脉动流能量耗散的抑制作用较为次要。     

Correlation between equation of state and temperature and pressure dependence of self-diffusion coefficient of polymers and simple liquids

Correlation between the equation of state and the temperature dependence of the self-diffusion coefficient D for polymers such as polystyrene (PS) and polydimethyl siloxane (PDMS) and simple liquids such as argon, methane and benzene and the pressure dependence of D for oligomers such as dimethyl siloxane (DMS) and simple liquids such as cyclohexane and methanol has been examined based on the equation of state derived previously. The experimental data used were published by Antonietti et al. and McCall et al. for polymers, by McCall for linear dimethylsiloxanes and by Jonas et al. and Woolf et al. for simple liquids. The expression for D in this work is given by

where A₁(M) is a function of molecular weight M_w, C₁(T) and P₁(T) are functions of temperature and B₁, n₁ and m₁ are constants determined experimentally. For simple liquids, the values of n₁ obtained range from 0.3 to 1.2, with an average , and m₁ is in the range 0.5–1.2, with . For polymers, values of n₁ are in the range 2.5–7.0 for PS and 0.5–1.3 for PDMS and m₁ for DMS is in the range 0.8–1.0. The relation Dη/T = f(M) is found to be useful for simple liquids over a wide range of temperature including the critical region and for pressures up to ≈5 kbar

1 kbar = 100 MPa There is a close correlation between ln(D/T) and _p and β_T through ln(D/T)ln D_c−⁻¹_p−β⁻¹_T, where D_c is D at the critical temperature and _p and β_T are the thermal expansion coefficient and compressibility, respectively. The molecular weight dependence of D for polymers and simple liquids is discussed based on the experimental data and recent theory of Doi and Edwards. A new model for the mechanism of self-diffusion in the liquid state is proposed.     

Three-dimensional numerical simulation method for gas–solid injector

A three-dimensional turbulent gas–solid two-phase flow model for a gas–solid injector is developed in the present study. Time-averaged conservation equation for mass and momentum and a two-equation k– closure are used to model the carried fluid phase. The solid phase is simulated by using a Lagrangian approach. In this model, the drag and lift forces on particles, the multi-body collisions among particles and the mutual interaction between gas and particles were taken into account. Interparticle interactions and particle–wall collisions are emulated by using the three-dimensional distinct element method (DEM). A new correlation, which represents the transfer of kinetic energy of the particle motion to kinetic energy of the carrier fluid, is introduced in the additional source term S_d of the transport equation of turbulence kinetic energy, K. The calculated pressure distributions along the axis in the different parts of gas–solid injectors using pressured pneumatic conveying system under different driving jet velocities, pressures and values of angle of convergent section () are found to be in agreement with the experimental results. The axial mean velocity of particles and the behavior of gas and particles in the gas–solid injector are calculated, their results reasonably explaining actual phenomenon observed in experiment.     

Modeling of Particle Removal using Non-contact Brush Scrubbing in Post-CMP Cleaning Processes

Particle removal using non-contact brush scrubbing for post-CMP (Chemical Mechanical Planarization) cleaning is investigated analytically. The removal of SiO₂ and Al₂O₃ particles adhered onto SiO₂ film coated on the wafer surface are considered. The cleaning fluid (H₂O/NH₄OH = 1:25 and 1:200) flowing between the brush and wafer surface is treated as a thin-film fluid flow. The flow field details and its effect on the drag force acting on the adhered particles are discussed. In addition to the drag force, the electrical double layer (EDL) and thermophoretic force effects on particle removal are also considered. It was found that the dominant force in achieving particle removal using a rolling mechanism is the drag force. The EDL and thermophoretic forces have an insignificant effect on particle removal. Based on the results from this study, particles of submicron size can be removed from a wafer surface using higher brush rotation speed and pure deionized (DI) water as the cleaning fluid.     

Gas-Liquid Mass Transfer Characteristics in a Gas-Liquid-Solid Bubble Column under Elevated Pressure and Temperature

abstract The volumetric mass transfer coefficient kLa of gases (H2, CO, CO2) and mass transfer coefficient kL on liquid par-affin side were studied using the dynamic absorption method in slurry bubble ...