非牛顿流体中气泡群传质的研究

CO2气泡群在液相中的传质在化工过程中广泛存在.对CO2气泡群在3种不同流体(牛顿流体、非弹性剪切变稀流体和黏弹性剪切变稀流体)中的气液传质过程进行了研究.利用CO2探针测定了不同操作条件下CO2的体积传质系数,考察了液相浓度,气体流量以及流变性质对体积传质系数的影响.结果表明:在3种流体中,体积传质系数均随气体流量的...     

鼓泡反应器中幂律型流体流动与传质特性

很多废水处理装置涉及非牛顿型流体中的多相流动和传质问题,研究其中的气液传质过程有助于实现装置的优化设计和高效节能运行。以鼓泡反应器内清水和不同质量分数的羧甲基纤维素钠（CMC）水溶液为实验对象,分别研究气相表观气速和液相流变特性对气泡尺寸分布、全局气含率和体积氧传质系数的影响。实验结果表明,液相的流变特性对其传质特性参数均有较大影响。与清水相比,CMC水溶液中气泡平均直径和分布范围更大;清水和CMC水溶液的全局气含率均随表观气速的增加而增大;CMC水溶液的体积氧传质系数随CMC水溶液质量分数的增加而减小。基于实验研究,得出修正的体积氧传质系数公式和适用于幂律型非牛顿流体流动体系氧传递过程的无量纲关联式,可很好地实现非牛顿流体流动的废水处理装置中气液传质参数的计算。     

鼓泡反应器中幂律型流体流动与传质特性

很多废水处理装置涉及非牛顿型流体中的多相流动和传质问题,研究其中的气液传质过程有助于实现装置的优化设计和高效节能运行。以鼓泡反应器内清水和不同质量分数的羧甲基纤维素钠(CMC)水溶液为实验对象,分别研究气相表观气速和液相流变特性对气泡尺寸分布、全局气含率和体积氧传质系数的影响。实验结果表明,液相的流变特性对其传质特性参数均有较大影响。与清水相比,CMC水溶液中气泡平均直径和分布范围更大;清水和CMC水溶液的全局气含率均随表观气速的增加而增大;CMC水溶液的体积氧传质系数随CMC水溶液质量分数的增加而减小。基于实验研究,得出修正的体积氧传质系数公式和适用于幂律型非牛顿流体流动体系氧传递过程的无量纲关联式,可很好地实现非牛顿流体流动的废水处理装置中气液传质参数的计算。     

拟塑性非牛顿流体中在线气泡聚并规律

以拟塑性羧甲基纤维素钠(CMC)水溶液作为非牛顿流体,对在线上升气泡的聚并规律进行了研究。利用光电信号采集系统测定了不同高度的气泡聚并分布规律,分析了气体速度及流体性质等因素对聚并规律的影响。结果表明,在测量高度和实验气速范围内,随着高度升高,在高气速下,气泡聚并率减小,在低气速下,则先增大后减小。2种情况下,达到一定高度后均趋于恒定;在一定高度下,达到一定气速后,气泡聚并率变化较小;中低气速下,聚并率随CMC质量分数增大而减小,而在高气速下,CMC质量分数变化对聚并率影响较小。     

固含率对沸腾床反应器气泡行为的影响

采用动态气体逸出法,在高7.0 m、直径0.3 m的有机玻璃塔中研究了固含率对沸腾床反应器内气泡行为特性的影响。在表观气速2.16~21.62 cm/s和固含率9.8%~39.0%（体积分数）范围内测定了反应器内的总气含率、大小气泡含率、大小气泡上升速度及其尺寸等参数。结果表明：总气含率随着表观气速的增大而增大,随着固含率的增大而减小。随着表观气速的增大,大气泡含率、大气泡直径及其上升速度均呈增大趋势;小气泡含率明显增大,但小气泡上升速度和直径趋于减小。随着固含率的增大,大气泡含率略有降低,但大气泡直径及其上升速度都明显增大;当固含率超过19.5%（体积分数）后,小气泡上升速度几乎下降为0;当固含率达到29.3%（体积分数）时,小气泡基本消失。     

固含率对沸腾床反应器气泡行为的影响

采用动态气体逸出法,在高7.0 m、直径0.3 m的有机玻璃塔中研究了固含率对沸腾床反应器内气泡行为特性的影响。在表观气速2.16~21.62 cm/s和固含率9.8%~39.0%(体积分数)范围内测定了反应器内的总气含率、大小气泡含率、大小气泡上升速度及其尺寸等参数。结果表明:总气含率随着表观气速的增大而增大,随着固含率的增大而减小。随着表观气速的增大,大气泡含率、大气泡直径及其上升速度均呈增大趋势;小气泡含率明显增大,但小气泡上升速度和直径趋于减小。随着固含率的增大,大气泡含率略有降低,但大气泡直径及其上升速度都明显增大;当固含率超过19.5%(体积分数)后,小气泡上升速度几乎下降为0;当固含率达到29.3%(体积分数)时,小气泡基本消失。     

采用电阻层析成像技术测量气液加压鼓泡塔局部气泡参数

在内径0.3 m,高6.6 m的加压气液鼓泡塔反应器中,采用电阻层析成像技术(ERT)研究了空气-水体系中气泡群平均上升速度、局部气含率及其径向分布。在表观气速0.119~0.312 m s 1,压力0.5~2.0 MPa,考察了表观气速、压力对气泡群上升速度、局部气含率及其径向分布的影响。实验结果表明,鼓泡塔中局部气含率随着表观气速与压力的增大而增大,其径向分布呈现出中心高边壁低的分布特征,但整个截面的分布并非严格对称,在r/R=0~0.3,气含率变化较小,且极大值出现在该范围内;气泡群的局部上升速度随着表观气速的增大而增大,但是随着压力的增大而减小。     

ILAR中醇及电解质对非牛顿流体中气-液传质的影响

在-气升式内环流反应器中试验考察了非牛顿流体羧甲基纤维素钠(CMC)中的气泡聚并现象以及表面活性物质对液相体积传质系数的影响。结果表明,非牛顿流体中气-液传质效率随黏度的增加而降低,其原因是黏度增加使Taylor泡的尾流趋于稳定,降低了液相扰动,气泡间易聚并,从而气-液传质效率低。向非牛顿流体中添加醇类物质会影响气-液传质行为,对于聚合物含量低的流体,添加微量醇可以促进气-液传质,聚合物含量高的非牛顿流体,微量醇的加入反而不利于气-液间传质过程。非牛顿流体在ILAR上升管中的气含率随着黏度的增加变化不大,而下降管中的气含率有所提高。     

牛顿及非牛顿流体中的气泡生成与对比

采用激光成像结合CCD摄像技术分别对牛顿及非牛顿流体(甘油和羧甲基纤维素钠水溶液)中的气泡生成行为进行了研究,对2种流体气泡生成过程中气泡形状和体积变化进行了比较。分析了非牛顿流体的弹性效应对气泡生成过程气泡形状的影响。实验结果表明,在实验条件范围内,甘油中,气泡生长初期,气泡体积增加较快,到了后期,增加幅度减缓,气速对气泡生长过程气泡体积影响很小;羧甲基纤维素钠(CMC)水溶液中,气泡生长初期,气泡缓慢生长,气速对气泡体积影响很小,到了后期,气泡体积增加幅度变大,气泡体积随着气速的增大而增大。     

鼓泡塔反应器的两级气泡模型参数研究

为了研究鼓泡塔反应器两级气泡模型在高黏度下的适用性,采用动态气体逸出法,在内径为286 mm,总高为7 200 mm的鼓泡塔中考察了液体黏度(1.2×10-3—210.4×10-3Pa·s)和操作条件对塔内总气含率,大、小气泡相含率和大、小气泡上升速度等两级气泡模型参数的影响。结果表明:床层总气含率随表观气速的增加而增大,大气泡相含率受液体黏度的影响较小,受表观气速的影响较大;小气泡相含率随黏度的增加而迅速下降,在高气速时受表观气速的影响较小。大、小气泡上升速度均随液体黏度的增加而降低,但随表观气速的升高有着不同的变化关系:前者明显升高,后者略有降低。大气泡直径随着黏度增大而稍有增大,小气泡直径随着黏度增大急剧减小。     

Radial Profiles of Gas Bubble Behavior in a Gas‐Liquid Bubble Column Reactor under Elevated Pressures

The effects of operating conditions on radial variation of gas holdups, bubble swarm rising velocity, and Sauter mean diameter were investigated in a bubble column reactor under elevated pressures using a conductivity probe method. Air served as gas phase and tap water as liquid phase with varying gas velocity and pressure. All three parameters increased constantly with higher superficial gas velocity. Maximum holdup, velocity, and Sauter mean diameter were found at the center of the cross section. Two different cases for Sauter mean diameter distribution were observed. The gas holdups increase continuously with higher system pressure, but decrease for bubble swarm rising velocity and Sauter mean diameter. According to experimental results, an empirical correlation of the gas holdup profiles is presented.     

Effects of viscosity and relaxation time on the hydrodynamics of gas–liquid systems

Effects of liquid properties on the hydrodynamics of gas–liquid systems were investigated in lab-scale bubble column (BC) and internal loop airlift (ILA). Alginate solutions, a glycerol solution and a Boger fluid were adopted to separately address the effects of viscosity and of surface tension for Newtonian fluids, and the effects of relaxation time for non-Newtonian fluid characterized by approximately constant viscosity (low shear thinning). Hydrodynamic regimes were characterized in terms of overall gas holdup, gas–liquid mass transfer coefficient, drift-flux and liquid circulation velocity. The superficial gas velocities at the transition between hydrodynamic regimes (homogenous regime–vortical-spiral regime–heterogeneous regime) as a function the liquid viscosity was characterized by a maximum. The same behavior was observed for the maximum stable gas holdup and gas–liquid mass transfer coefficient in BC. Viscosity enhances homogeneous regime stability for μ<4.25 mPa s, in BC, and μ<7.68 mPa s, in ILA. For non-Newtonian fluids the transition velocity increases with liquid elasticity. The stabilization mechanism related to the relaxation time of Boger fluids has been discussed.     

Bubble Behavior of a Large‐Scale Bubble Column with Elevated Pressure

Gas holdups and the rising velocity of large and small bubbles are measured using the dynamic gas disengagement approach in a pressured bubble column of 0.3 m in diameter and 6.6 m in height. The effects of superficial gas velocity, liquid surface tension, liquid viscosity, and system pressure on the gas holdups and the rising velocity of small and large bubbles are investigated. The holdup of large bubbles and the rising velocity of small bubbles increase with increasing liquid viscosity and liquid surface tension. Meanwhile, the holdup of small bubbles and the rising velocity of a swarm of large bubbles decrease. Moreover, the holdup of large bubbles and the rising velocity of a swarm of small bubbles decrease with increasing system pressure. A correlation for the holdup of small bubbles is obtained from experimental data.     

HOLDUP STRUCTURE IN HIGHLY VISCOUS NEWTONIAN AND NON-NEWTONIAN LIQUIDS IN BUBBLE COLUMNS

Gas holdup structures in highly viscous glycerine and CMC solutions are studied in a 0.305 m diameter batch bubble column. The fractional gas holdups are determined using the dynamic gas disengagement method. Empirical correlations for the gas holdup based on data covering wide ranges of viscosities in Newtonian and pseudoplastic non-Newtonian solutions are presented. For highly viscous pseudoplastic solutions in small diameter columns, the gas holdup has a square root dependence on the diameter of the column. The absence of small bubbles is suggested to be a reason for the very low volumetric mass transfer coefficients in highly viscous solutions, reported in the literature.     

HOLDUP STRUCTURE IN HIGHLY VISCOUS NEWTONIAN AND NON-NEWTONIAN LIQUIDS IN BUBBLE COLUMNS

Gas holdup structures in highly viscous glycerine and CMC solutions are studied in a 0.305 m diameter batch bubble column. The fractional gas holdups are determined using the dynamic gas disengagement method. Empirical correlations for the gas holdup based on data covering wide ranges of viscosities in Newtonian and pseudoplastic non-Newtonian solutions are presented. For highly viscous pseudoplastic solutions in small diameter columns, the gas holdup has a square root dependence on the diameter of the column. The absence of small bubbles is suggested to be a reason for the very low volumetric mass transfer coefficients in highly viscous solutions, reported in the literature.     

加压大型鼓泡床反应器内大小气泡气含率研究

在内径0.3m、高6.6m的加压鼓泡床反应器内采用床层塌落技术测量床层内的大小气泡气含率实验。由于大小气泡上升速度不同,床层塌落曲线存在一水平段,在此基础上,详细考察了表面张力、粘度、系统压力、表观气速对大小气泡气含率的影响,得出大气泡气含率随粘度和表面张力升高而升高,随压力升高而降低;小气泡气含率随粘度和表面张力升高而降低,随压力升高而升高;并根据质量守恒定理,进行了解释。     

Structure of trickle-to-pulse flow regime transition and pulse dynamics at elevated temperature in slow-mode cyclic operation

The effects of temperature and pressure on the structure of the trickle-to-pulse flow regime transition in slow-mode cyclic operation in trickle-bed reactors were reported. The relationship between liquid holdup and liquid velocities at the trickle-to-pulse flow transition in cyclic operation, the shock wave behavior as a function of bed depth, as well as the pulsing flow regime properties were investigated for Newtonian (air-water) and non-Newtonian (air-0.25% carboxymethylcellulose (CMC)) liquids. At a given temperature, the breakthrough, plateau and decay times of the shock wave were found to decrease with bed depth. The pulse velocity and pulse frequency for pulsing flow regime both in cyclic operation and in natural pulsing (constant-throughput operation) were observed to increase with temperature. However, increasing the reactor pressure led to increased pulse frequency and decreased pulse velocity. Analysis of the transition liquid holdups for natural pulse flow and cyclic operation revealed that the liquid holdup decreased with temperature and pressure. The transition liquid holdups and superficial liquid pulse velocities in symmetric peak-base cyclic operation surpassed those in constant-throughput operation for given temperature, pressure and gas velocity, giving rise to wider trickle flow regime area in cyclic operation. The behavior of both Newtonian and power-law non-Newtonian fluids was similar regarding the effect of temperature, pressure and gas velocity.     

Gas Holdup and Solid‐Liquid Mass Transfer in Newtonian and non‐Newtonian Fluids in Bubble Columns

Gas holdup and surface‐liquid mass transfer rate in a bubble column have been experimentally investigated. De‐mineralized water, 0.5 and 1.0% aqueous solutions of carboxy methyl cellulose (CMC), and 60% aqueous propylene glycol have been used as the test liquids. Effects of column diameter, liquid height to column diameter ratio, superficial gas velocity and liquid phase viscosity on gas holdup and mass transfer rate are studied. Generalized correlations for the average gas holdup and wall to liquid heat and mass transfer coefficients are proposed. These are valid for both Newtonian and pseudoplastic non‐Newtonian fluids.