磷酸三丁酯/煤油支撑液膜体系中苯酚的传质分离

研究了苯酚在以多孔聚丙烯平板膜(Celgard2500)为支撑体、磷酸三丁酯(TBP)为膜载体和煤油为膜溶剂的支撑液膜体系中的传质过程;用传统萃取法测定了TBP/煤油体系中苯酚络合物摩尔比为1∶1,同时得到25.0℃萃取平衡常数为96.72;考察了原料相pH值、初始质量浓度、膜二侧转速、载体浓度和反萃取相碱浓度对苯酚传质的影响,确定了该体系分离苯酚的最佳条件:原料相pH<9,苯酚初始质量浓度<1 000 mg/L,膜二侧转速>300 r/m in,载体浓度为0.55 mol/L,反萃取相碱浓度0.10 mol/L;根据双膜理论提出苯酚的传质动力学方程,采用直线斜率法计算了苯酚在TBP/煤油支撑液膜体系中的扩散层厚度和膜内扩散系数,计算结果表明动力学方程计算值能较好地与实验值吻合,平均相对误差在2%以内。     

LIX984N为载体的中空纤维更新液膜中铜的传递过程

以LIX984N为载体,煤油为稀释剂,H2SO4为反萃剂,研究了中空纤维更新液膜过程中铜的传递行为。考察了两相压差、铜离子浓度、两相流速、操作方式以及膜丝有效长度等对传质过程的影响。结果表明:膜丝两侧的操作压差对传质过程几乎没有影响;随着料液相中溶质Cu(Ⅱ)浓度的增大传质通量增大,而反萃相中的Cu(Ⅱ)浓度对传质过程几乎没有影响;传质通量会随着壳程料液流速的增大而增大,但管程侧反萃相的流速对传质过程影响很小;逆流和并流两种操作方式对传质过程的影响可以忽略,而膜丝有效长度的增加会导致单位面积平均传质通量的下降。     

膜接触器中乳化液膜脱除Ni2+的研究

研究了以D2EHPA/煤油/HC1形成的微乳液体系在中空纤维膜接触器中萃取NiCl2水溶液中Ni2的过程,考察了D2EHPA和Ni2+浓度、水溶液酸度、两相流速对溶液中Ni2+的萃取率和传质性能的影响.结果表明,用D2EHPA/煤油/HCl形成的微乳液体系能有效萃取NiCl2水溶液中的微量Ni2+,增大微乳液中载体D2EHPA浓度和料液pH都能提高Ni2的萃取率和过程的总质系数,增加料液流速能显著提高Ni2+的萃取率和过程的总质系数,表明过程的传质阻力主要在水溶液相.     

中空纤维支撑液膜技术处理含铜废水

重金属废水的处理在环境保护和重金属资源综合利用方面都受到广泛的关注.采用中空纤维支撑液膜技术,用CuSO4水溶液模拟工业含Cu(Ⅱ)废水,二(2-乙基己基)磷酸(D2EHPA)/煤油为液膜相,盐酸为接受相,研究了液膜相组成、两相流速、流动方式等因素对中空纤维支撑液膜过程传质性能的影响.结果表明,料液相在管程流动时的传质通量大于料液相在壳程流动时的传质通量,传质通量随着管、壳程两相流速的增大及液膜相中载体浓度的增加而增大.模拟实验结果表明,中空纤维支撑液膜技术可同时实现废水中Cu(Ⅱ)的去除与浓缩,处理效果好.废水中Cu(Ⅱ)的去除率达97%以上,富集液中Cu(Ⅱ)浓缩倍数达5倍以上.     

PTFE中空纤维膜萃取对苯二胺工艺研究

以硫酸溶液为萃取剂,采用PTFE中空纤维膜萃取料液中的对苯二胺,考察了料液相对苯二胺的初始浓度、料液相初始pH、料液相与萃取相流量、萃取剂的初始浓度对对苯二胺萃取率(η)的影响。结果表明,随着料液初始浓度增大,η增大,当对苯二胺浓度0.8 g/L时,η减小,但膜通量基本不变,即存在一个最大膜通量,此时对苯二胺浓度变化对传质无影响;对苯二胺料液的pH增大,η增大;萃取相硫酸浓度增大,η增大。另外,温度升高有利于膜萃取。     

组合液膜分离镉锌的动力学分析

采用膜相和反萃相分别为三正辛胺的煤油溶液和醋酸胺的水溶液的组合液膜体系,研究了氯化物料液中镉、锌离子的分离.结果发现,传质过程主要由料液相侧水扩散层和膜相的扩散过程控制;迁移20 h后,镉离子迁移率可达98.3%,锌离子迁移率只有2%,分离系数为49.2.组合液膜能很好地分离镉、锌.流失到料液相和反萃相的载体浓度测试表明,组合液膜中,双固体膜能阻止膜相中载体的流失,提高膜的稳定性,延长膜寿命.改变三正辛胺浓度,对镉离子传输的动力学过程进行了分析,建立了镉离子传输的动力学方程.     

PTFE中空纤维膜萃取苯甲酸工艺研究

以氢氧化钠溶液为萃取剂,采用PTFE中空纤维膜萃取料液中的苯甲酸,考察了料液相苯甲酸的初始浓度、料液相初始pH、料液相与萃取相流量比、萃取剂的初始浓度对苯甲酸萃取率(η)的影响。结果表明,随着料液初始浓度增大,η增大,当苯甲酸浓度1 g/L时,η减小,但膜通量基本不变,即存在一个最大膜通量,此时苯甲酸浓度变化对传质无影响;料液的pH值下降,η增大;萃取相氢氧化钠浓度增大,η增大;存在一个最佳相流量比(Q料/Q萃)为1.8。另外,温度升高有利于膜萃取。     

PTFE中空纤维膜萃取烟酸工艺研究

以氢氧化钠溶液为萃取剂,采用PTFE中空纤维膜萃取料液中的烟酸,考察了料液相烟酸的初始浓度、料液相初始pH值、料液相与萃取相流量比、萃取剂的初始浓度对烟酸萃取率(η)的影响。结果表明,随着料液初始浓度增大,η增大,当烟酸浓度0.9 g/L时,η减小,但膜通量基本不变,即存在一个最大膜通量,此时烟酸浓度变化对传质无影响;烟酸料液存在一个最佳pH值为4~5;萃取相氢氧化钠浓度增大,η增大;存在一个最佳相流量比(Q料/Q萃)为2.1;温度升高有利于膜萃取。     

聚丙烯支撑液膜提取柠檬酸的传质条件

用聚丙烯支撑液膜从柠檬酸溶液中提取柠檬酸，通过正交实验考察和分析料液相浓度、反萃取相浓度、搅拌速率、温度等因素的影响，得到最佳传质条件：料液相浓度为0．4mol／L、反萃取相浓度0．1mol／L、搅拌强度300r／min、传质温度25℃。同时对该膜体系进行连续提取实验，结果表明最佳传质条件下膜体系稳定性较好，膜通量下降后可通过重新浸泡得以恢复，继续使用。     

大块液膜技术处理含六价铬废水

以磷酸三丁酯(TBP)为载体,煤油为稀释剂,NaOH为反萃剂,采用大块液膜技术处理含95~100mg/LCr(VI)的模拟废水。考察了液膜相用量、载体体积分数及反萃剂浓度对大块液膜过程中Cr(VI)传质过程的影响。结果表明,大块液膜技术对废水中Cr(VI)的去除效果较好。Cr(VI)迁移速率随TBP体积分数的提高而加快。当反萃剂NaOH浓度大于0.5mol/L时,反萃剂浓度对Cr(VI)传质过程的影响较小。处理后废水中Cr(VI)含量降至0.5mg/L以下,达到国家排放标准。     

Flüssigmembran-Technik – Übersicht über Phänomene,Transportmechanismen und Modellbildungen

Liquid membrane technology – A survey of associated phenomena, transport mechanisms, and models. Liquid membrane permeation is the name given to a simultaneous extraction/stripping process. A summary of related phenomena, mass transfer, and models is presented. A new model has been developed to describe mass transfer in liquid membranes, in which the spherical droplets serve as reaction centres. An account of present applications demonstrates the limitations of liquid membrane processes.     

Mass transfer of phenol through supported liquid membrane

The separation of phenol from the aqueous solution was carried out at 25°C in a supported liquid membrane of batch type using benzene or dibenzo-18-crown-6 as carrier in the phenol-NaOH system. The mass transfer of phenol was investigated with a theoretical model based on the mass transfer with or without chemical reaction in the stripping side. Pseudo-first-order reaction type was used to measure overall and individual mass transfer coefficients of phenol. The influence of initial concentration of carrier on overall mass transfer coefficient was found to be more significant than those of agitation speed and initial concentrations of phenol and NaOH solutions. The numerical analysis of facilitated transport of phenol through liquid membrane gave a result that the chemical reversible reaction between phenol and carrier in the liquid membrane side was fallen into the region between fast and slow reaction with the tendency to be much closer to the slow reaction region.     

Permeation study on the hollow-fiber supported liquid membrane for the extraction of Cobalt(II)

The transport of Co(II) through hollow-fiber-supported liquid membrane containing di-(2-ethylhexyl) phosphoric acid (D2EHPA) diluted in kerosene was examined. The mass transfer rate, expressed as permeability, P, focused on diffusion through the aqueous layer in the feed solution, the organic layer and the aqueous layer in the stripping solution. Experiments were performed as a function of aqueous feed solution velocity (100-500 ml/min), carrier concentration (0.1-20% v/v), aqueous stripping solution velocity (100-1,000 ml/min) and feed concentration (100-1,000 ppm) with 0.1 M HCl in the product phase. pH of the feed solution was 5.0. The measured permeabilities were compared to generally accepted mass transfer correlations. The validity of the prediction was evaluated with the experimental data, and the data were found to tie in well with the theoretical values. The model is the reported describing that the rate limiting step in the transport of the ion was the diffusion through both aqueous films, feed and stripping, whereas the organic resistance of the membrane was negligible. From this study, the model has good potential for the prediction of permeability of Co(II).     

硅橡胶复合膜用于含酚水溶液渗透萃取传质过程

以苯酚为模型污染物,以氢氧化钠溶液为萃取液,利用平板复合膜［聚二甲基硅氧烷（PDMS）/聚偏氟乙烯（PVDF）］构造渗透萃取体系,系统地研究了该体系渗透萃取含酚水溶液的传质过程与特性。探讨了料液与萃取液的浓度及流量、运行温度等操作条件及活性层厚度对渗透萃取传质性能的影响。结果表明,pH>13时,总传质系数K_ov不随萃取液流量及浓度变化而变化;苯酚的液膜传质系数kf与膜面流动Reynolds数Re^0.46呈正比,传质通量与温度符合Arrhenius方程。在苯酚初始浓度5.0～15.0 g&#8226;L^-1范围内,K_ov为定值。活性皮层厚度为4、6、8 μm的膜扩散传质系数分别为15.0×10^-7、9.9×10^-7及7.5×10^-7m&#8226;s^-1（323.2 K）,较均质膜提高了2～4倍。苯酚在复合膜中的传质仍属膜阻控制的传质。     

Cobalt Recovery from Sulfate Media Applying a Liquid Membrane Containing Cyanex 302

Cobalt recovery from sulfate solutions was studied by using a liquid membrane containing Cyanex 302. The influence of the pH and the concentrations of cobalt and the extractant on the metal equilibrium distribution was established. Kinetic investigations of the cobalt transfer across a liquid membrane containing Cyanex 302 were performed in a rotating film contactor. Sulfuric acid was used as a stripping agent. The results obtained show that cobalt can be successfully recovered from neutral and weakly acidic sulfate solutions. A mathematical model describing the transport of cobalt ions across the liquid membrane was proposed. The local mass transfer coefficients of cobalt ions in the aqueous phases and cobalt‐carrier complex in the organic phase were evaluated on the basis of the experimental data obtained at various conditions as well as on the proposed model.     

Stability and extraction study of phenolic wastewater treatment by supported liquid membrane using tributyl phosphate and sesame oil as liquid membrane

Phenols pose a risk to the environment and to human health. Phenol and its derivatives are toxic pollutants, frequently found in surface and tap waters, and in aqueous effluents from various manufacturing processes. In this paper, an experimental study regarding transport of phenol through a supported liquid membrane (SLM) using tributyl phosphate (TBP) and sesame oil as liquid membrane (LM) was performed. Factors affecting permeation of phenol such as initial phenol concentration, carrier concentration, feed phase pH and stripping phase concentration were analyzed using Taguchi method. Optimal experimental condition of phenol transport was obtained using analysis of variance (ANOVA) after 7 h extraction (feed concentration: 200 mg/L; carrier concentration (%TBP): 40%; feed pH: 2; strip phase concentration: 1.1 M). Mass transfer coefficient for this system was evaluated, and compared with similar works, and it was shown that it has the highest mass transfer rate. In addition to transport study, stability of the membrane was investigated by examination of stripping phase concentration, carrier concentration and salt concentration effects.     

Performance of hollow fiber supported liquid membrane on the extraction of mercury(II) ions

The extraction and recovery or stripping of mercury ions from chloride media using microporous hydrophobic hollow fiber supported liquid membranes (HFSLM) has been studied. Tri-n-octylamine (TOA) dissolved in kerosene was used as an extractant. Sodium hydroxide was used as a stripping solution. The transport system was studied as a function of several variables: the concentration of hydrochloric acid in the feed solution, the concentration of TOA in the liquid membrane, the concentration of sodium hydroxide in the stripping solution, the concentration of mercury ions in the feed solution and the flow rates of both feed and stripping solutions. The results indicated that the maximum percentages of the extraction and recovery of mercury ions of 100% and 97% were achieved at the concentration of hydrochloric acid in the feed solution of 0.1 mol/l, the concentration of TOA at 3% v/v, the concentration of sodium hydroxide at 0.5 mol/l and the flow rates of the feed and stripping solutions of 100 ml/min. However, the concentration of mercury ions from 1–100 ppm in the feed solution had no effect on the percentages of extraction and recovery of mercury ions. Thus, these results have identified that the hollow fiber supported liquid membrane process has high efficiency on both the extraction and recovery of mercury (II) ions. Moreover, the mass transfer coefficients of the aqueous phase (k _i ) and membrane or organic phase (k _m ) were calculated. The mass transfer coefficients of the aqueous phase and organic phase are 0.42 and 1.67 cm/s, respectively. The mass transfer coefficient of the organic phase is higher than that of the aqueous phase. Therefore, the mass transfer controlling step is the diffusion of the mercury ions through the film layer between the feed solution and the liquid membrane.     

Analysis of Extraction of Cu(II) by Strip Dispersion Hybrid Liquid Membrane (SDHLM) using PMBP as Carrier

A liquid membrane system, denoted a strip dispersion hybrid liquid membrane (SDHLM) containing 1‐phenyl‐3‐methyl‐4‐benzoyl‐pyrazolone –5 as carrier in xylene, was reported for the transport and separation of Cu(II) from Zn (II) ions. The effects of various factors on the transport of copper(II) ions through SDHLM were systematically investigated by orthogonal tests. The optimum transport conditions of copper ions were summarized. In the overall mass transfer process the mass transfer resistance due to the aqueous boundary layer diffusion and diffusion in the microporous membrane is dominant. The accumulation of the Cu(II)‐carrier coordination compound in the membrane shows that the transfer in SDHLM possesses the characteristic of nonequlibrium mass transfer in this study. The rheologic experiments verified that the organic phase in the SDHLM system was the non‐Newtonian fluid and the organic phase after transport of 6 hr was a system of thixotropy in our experimental conditions. The lag ring experiments proved that the thixotropy of the organic phase in the SDHLM system was relevant to the composition of the membrane. In the experimental comparison of two types of liquid membrane, SDHLM has superiority over SLM in respect of transport flux, permeability coefficient, recovery percentage or concentration of solute in the stripping solution, efficiency of uphill transport, loss of membrane solution, and the separation efficiency of the membrane.     

Mass transport with varying diffusion- and solubility coefficient through a catalytic membrane layer

Mass transport, accompanied by chemical reaction through membrane reactor has been investigated in the case of varying diffusion coefficient and solubility coefficient. In reality, both parameters might depend on the concentration and/or on the inhomogeneity of the membrane layer. General mathematical models were developed to describe the mass transport, taking into account the external mass transfer resistances as well, when the solubility coefficient can vary, e.g. according to the Langmuir–Hinschelwood adsorption theory or when the value of diffusion coefficient depends on the concentration/anisotropy in the membrane. A general solution has been given that can be applied to most of the mathematical functions of the parameters mentioned. The concentration distribution and the mass transfer rate will be given in closed mathematical forms. The value of the mass transfer rates could be strongly altered by the varying diffusion- and/or solubility coefficient. The mathematical model and the effect of the varying parameters have been discussed in this paper.