采用纳米Al203和碳纳米管颗粒强化CO2吸收的理论及实验研究（英文）

The influence of nano-particles on CO2 absorption was studied experimentally in a stirred thermostatic reactor. Nano-A1203 and carbon nanotube （CNT） particles which showed different hydrophobic properties were chosen for the investigation. The experimental results were compared with that of micron-size activated carbon （AC） and Al2O3 particles. From the results, no enhancement by micron-size A1203 was found, and with the increase of A1203 concentration, the enhancement factor decreased. However, nano-Al203 showed a weak enlaancement tor me COz absorption. AC and CNT particles all intensified the gas-liquid mass transfer effectively, yet the trend of the enhancement factor with stirring speed for the two particles was different. With increasing stirring speed, the enhancement factor of AC particles was decreased, wl＇iereas in CNT suspensions it was increased. The experimental phenomena demonstrated a difference in enhancement mechanism for different size particles. For nano-particles, besides the influence of adsorbability and hydrophobicity, the micro-convection caused by Brownian motion should be also taken into account. Considering the micro-convection effect, a theoretical model was developed to shed light on the absorption enhancement bv nano-oarticles.     

活性炭粒子对K2CO3溶液中CO2化学吸收的强化

The enhancement of chemical absorption of CO2 by K2CO3/H2O absorbents in the presence of activated carbon （AC） particles was investigated. The results show that the gas absorption rates can be enhanced significantly in the presence of AC particles, and the maximum enhancement factor 3.7 was observed at low stirring intensities. The enhancement factor increased rapidly with the solid loading during the initial period of absorption and then be- came mild gradually to a maximum value. Both the liquid-solid contact area and the probability of solid particles residing at the gas-liquid interface decreased with the increase of the particle size, leading to a negative effect on the enhancement of mass transfer. The influence of the particles on gas absorption decreased with the reaction rate. The stirring speed changed the interfacial coverage and mass transfer rate on the liquid side and consequently affected the mass transfer between the gas and liquid phases; the enhancement factor decreased with the stirring intensity. A heterogeneous two-zone model was proposed for predicting the enhancement factor and the calculated results agreed well with the experimental data.     

第三分散相液滴增强气体吸收的一维非稳态非均相传质模型

A model for one-dimensional unsteady heterogeneous mass transfer was developed based on Danckwerts’ surface renewal theory in order to describe the mass transfer enhancement of absorption process for a slightly soluble gas in a gas-liquid-liquid system. The model accounts for the mass transfer resistance within the dispersed phase and the effect of emulsion viscosity on mass transfer. An analytical solution for enhancement factor was obtained by Laplace domain transformation. The absorption rates of carbon dioxide in the dodecane-in-water and castor oil-in-water systems were measured in a thermostatic reactor, and the enhancement factors were calculated at different volume fractions of dispersed phase and stirrer speeds. The model predictions agree well with the experi-mental data.     

搅拌式有限氧补偿条件下乳状液中多不饱和脂肪酸氧化模型

The oxidation of polyunsaturated fatty acids （PUFA） in emulsion with stirring and limited oxygen compensation was studied. A mathematical model of diffusion-oxidation was developed considering the mass transfer resistance of a gas-liquid boundary, the resistance of the boundary layer from the emulsifier membrane, and the autocatalytic-type autoxidation reaction of PUFA. The dynamic mass transfer coefficient of the emulsifier membrane, k0, was introduced. The model was verified by comparing the predictions of the model with the experi- mental data. The results indicated that the model was in good agreement with the oxygen diffusion and linoleic acid oxidation in the emulsion, and showed good applicability in the prediction of the effect of the emulsifier type on the oxidation of PUFA in the emulsion. It indicated that the oxidation of PUFA in emulsions, with stirring and limited oxygen compensation from the atmosphere, was controlled mostly by mass transfer resistance from the emulsifier membrane.     

Mass transfer area in a multi-stage high-speed disperser with split packing

In this study, the mean droplet diameter in the cavity zone and the total mass transfer area of a multi-stage highspeed disperser(HSD) reactor with different packing combinations were measured and evaluated. The effects of rotational speed and packing radius, as well as the packing ring radius and numbers, on the mean droplet diameter and the total mass transfer area were evaluated. A model was established to calculate the mass transfer area in the cavity zone in the HSD reactor, and it was found that the packings contribute 61%–82% of the total mass transfer area. A correlation for predicting the mass transfer area in the packing zone was regressed by the dimensionless analysis method. An enhancement factor based on the mass transfer area in the packing zone was proposed to evaluate the effect of packing combination on mass transfer area. Two optimum packing combinations were proposed in consideration of the mean droplet diameter and the enhancement factor.     

多项体系气体吸收的三维非均相传质模型

A three-dimensional heterogeneous mass transfer model was proposed to investigate the enhancement of dispersed particles on gas absorption. The strategy to calculate local and overall enhancement factors is proposed. Instead of a global grid, the composite overlapping grid is adopted, which simplifies the setup and solution of the three-dimensional model equations. It is found that dispersed particle hold-up, particle size, liquid-solid partition coefficient of transported component, characteristic contact time, and the shortest distance between particles and gas-liquid interface have major influence on absorption enhancement factor. The particle-particle interaction on gas absorption and the lateral diffusion of transported component in liquid film were studied with the multi-particle simulation. The proposed model predicted the experimental data from the literature reasonably well.     

机械力强化作用下轻烧氧化镁碳化过程的传质与反应动力学研究

The carbonization of magnesium oxide particles by CO2 was investigated using a stirring mill reactor. The effects of the system temperature, stirring rotation speed, influx rate of CO2 and initial diameter of the magnesium oxide particles on the carbonization process were determined, The results show that the system temperature and the stirring rotation speed are the most significant influencing factors on the carbonization rate. The determi-nation of critical decomposition temperature (CDT) gives the maximum carbonization rate with other conditions fixed. A theoretical model involving mass transfer and reaction kinetics was presented for the carbonization process. The apparent activation energy was calculated to be 32.8kJ·mol-1. The carbonization process is co-controlled by diffusive mass transfer and chemical reaction. The model fits well with the experimental results.     

加入分散有机相强化气体吸收的传质过程(英文)

Mass transfer enhancement of gas absorption by adding a dispersed organic phase has been studied in this work. Various dispersed organic phases (heptanol, octanol, isoamyl alcohol, heptane, octane, and isooctane) were tested respectively in the experiment. According to the theoretical model and experimental data, the overall volumetric mass transfer coefficient and enhancement factor were obtained under different dispersed organic phase volume fraction and stirring speed. The experimental results indicate that gas-liquid mass transfer is enhanced at different level by adding a dispersed organic phase. The best performance of enhancement were achieved with the dispersed organic phase volumetric fraction of 5% and under an intermediate stirring speed of 670 r·min-1. Among the organic phases tested in the experiment, alcohols show better performance, which gave 20% higher enhance-ment of overall volumetric mass transfer coefficient than adding alkanes.     

大气环境中静态小液滴对周围气体吸收的研究

Absorption of gaseous species into stationary droplets is a fundamental interest of mass transfer between liquid droplets and ambient gas, which plays a key role in atmospheric environment control and many industrial applications. In this paper, two different considerations including equilibrium and non-equilibrium relations at the interface are used to analyze and predict the absorption time for a physical absorption at a relatively low solubility of gas. For the equilibrium pattern, in the beginning period of absorption, the mass transfer rate is considerably rapid and afterward becomes slower and slower and finally comes to almost zero as the droplet concentration closes to the saturated value. Differently, when the non-equilibrium model is adopted, the interfacial concentration increases gradually with the bulk concentration of liquid droplet, and the absorption rate mildly decelerates with the increase of bulk one throughout the process, which leads to a longer absorption time. Based on the diffusion equation of species, the concentration distribution within the droplet at different times is computed. A solution for CO2 absorption into a small water droplet is given.     

甲基二乙醇胺水溶液在改进的湿壁塔上吸收二氧化碳的动力学模型

To get more accurate kinetic data of the absorption of CO2 into aqueous solution of N-methyldiethanolamine, a wetted wall column was modified to more uniformly distribute the liquid on the column surface and gas in the absorbing chamber and change the length of the column. The average liquid film thickness and the liquid-phase mass transfer coefficient were measured, and a correlation for the Sherwood number, Reynolds number and Schmidt number was obtained for the modified wetted wall column. The equilibrium concentrations in chemical reactions were calculated with a minor absolute error for calculating the rate constant more accurately. A mathematical model for the CO2 absorption was established based on the diffusional mass transfer accompanied with parallel reversible reactions, and the partial differential equation was solved by Laplace transform. An analytical expression for the concentration of carbon dioxide as a function of time and penetration depth in liquid film and the average interphase mass transfer rate was obtained. This model was also used to calculate the rate constant for a second-order reaction, which was in good agreement with reported data.     

水溶液中甲苯分散相增强难溶气体吸收

利用难溶气体的物理吸收过程,在具有恒定气液界面面积的吸收装置中研究了常压和室温条件下分散液相(甲苯)对气液传质的增强作用。通过测定气相(丙烷和氢气)压力随时间的变化,计算出液侧传质系数和传质增强因子。试验发现,当传质组分在分散液相与连续液相内的分配系数较大,或在两相间的相对扩散系数较大,且分散相形成的液滴较小时,加入分散液相可显著增强气液传质;增强因子随分散液相含率的增大而增大,但增大幅度逐渐减小;当气体在纯水中的传质系数增大时,同等条件下分散相对气液传质的增强作用减小。     

活性炭粒子对K2CO3溶液中CO2化学吸收的强化

The enhancement of chemical absorption of CO2 by K2CO3/H2O absorbents in the presence of activated carbon (AC) particles was investigated. The results show that the gas absorption rates can be enhanced significantly in the presence of AC particles,and the maximum enhancement factor 3.7 was observed at low stirring intensities.The enhancement factor increased rapidly with the solid loading during the initial period of absorption and then became mild gradually to a maximum value. Both the liquid-solid contact area and the probability of solid particles residing at the gas-liquid interface decreased with the increase of the particle size,leading to a negative effect on the enhancement of mass transfer. The influence of the particles on gas absorption decreased with the reaction rate. The stirring speed changed the interfacial coverage and mass transfer rate on the liquid side and consequently affected the mass transfer between the gas and liquid phases; the enhancement factor decreased with the stirring intensity. A heterogeneous two-zone model was proposed for predicting the enhancement factor and the calculated results agreed well with the experimental data.     

Experimental and Theoretical Studies of CO2 Absorption Enhancement by Nano-Al2O3 and Carbon Nanotube Particles

The influence of nano-particles on CO2 absorption was studied experimentally in a stirred thermostatic reactor. Nano-Al2O3 and carbon nanotube (CNT) particles which showed different hydrophobic propert...     

在搅拌器中油水乳状液的气液传质

选取CO2为气相,苯/辛烷-水乳状液为液相,通过难溶气体的吸收实验,研究了在带有气体分布器的三相混合吸收装置中分散液相对气液传质的增强作用。实验结果表明,传质增强因子随能量输入的增大而增大,且分散相形成的液滴较小时,在膜内停留时间里小液滴对气液传质有增强作用。分析了"传输机理",总结出增强气液传质的本质在于分散液相通过吸收作用改变气液界面液侧组分浓度梯度,并在此基础上提出了新的描述分散液相增强气液传质的解释。     

微细颗粒强化氧气吸收实验

引言目前,石灰石-石膏湿法烟气脱硫工艺是在燃煤电厂应用最广的烟气脱硫技术,脱硫的副产品是脱硫石膏(CaSO4.2H2O)。但在实际运行过程中由于氧化率未达到要求值,从而使得产生的石膏晶体不足,形成了亚硫酸钙和硫酸钙的混合晶体[1];另外,燃煤锅炉产生的烟气虽经除尘,但进入脱硫装置时仍含有大量粉尘颗粒[2-3]。因此,在电厂实际的脱硫过程中,发生的并不是单纯的两相     

活性炭/水浆料中CO2吸收过程的增强

针对分散相微粒增强难溶气体的吸收过程,提出了一个一维非稳态非均相传质的二区模型,并进行了理论求解。根据表面更新理论,得到了增强因子的数学表达式。利用恒温反应釜,对活性炭/水浆料中发生的CO2吸收过程进行了实验研究,测定了不同颗粒浓度及转速下的增强因子。实验结果与模型预测值吻合良好,表明本文模型具有很高的预测精度。     

A route for the study on mass transfer enhancement by adding particles in liquid phase

This work presents a route for the study on the absorption performance of gas into liquid under the condition of adding particles in a stirred constant temperature reactor. Two evaluated systems, hydrogen–water and hydrogen–methanol, with the addition of activated carbon particles (ACP) were carried out, respectively. The results showed that the addition of ACP into the water can enhance the mass transfer between hydrogen and water, the enhancement factor increases rapidly with the increase of the ACP content, and then tends to be unchanged. However, for the hydrogen–methanol system, ACP has little effect on the mass transfer performance. In addition, a gas–liquid mass transfer model considering the effect of solid particle enhancement was established based on the shuttle effect and two-film model. Results indicated that the predicted value agreed well with the experimental value in both hydrogen–methanol–ACP and hydrogen–water–ACP systems.     

微通道内单乙醇胺水溶液吸收CO2/N2混合气的传质特性

采用高速摄像仪对400 μm×400 μm T形微通道内单乙醇胺（MEA）水溶液吸收混合气中CO₂过程的气液两相流及传质特性进行了实验研究,微通道内的压力降采用压力传感器进行测量。考察了弹状流型下气液两相流量及MEA浓度对压力降、比表面积和传质性能的影响。结果表明,当MEA浓度不变,气液两相流量增大时,压力降、比表面积、传质系数、体积传质系数和增强因子均增大,并逐渐趋于恒定。当气液流量不变,MEA浓度增大时,压力降、传质系数、体积传质系数和增强因子增大,但比表面积减小。实验条件下,压力降范围为2.00~5.23 kPa,化学吸收过程的传质系数范围为7.74×10^-4~2.97×10^-3 m·s^-1。对于伴有快速化学反应的传质过程,以Sherwood数、Reynolds数、Schmidt数及增强因子为变量建立了体积传质系数的预测关联式,平均偏差为5.09%,具有良好的预测性能。