液体表面活性剂膜的传质模型

本文提出了一个新的关于液膜传质的模型.该模型不仅考虑了溶质在乳状液球内核中的渗透过程,还考虑了由表面活性剂所致的界面阻力升高效应,因而更加准确地描述了液膜体系的传质过程.该模型的另一个特点是考虑了在传质过程中膜的破裂,从而使数学模型更加迫近液膜体系的实际情况.实验结果与理论分析均表明,溶质透过乳状液外围的表面活性剂薄层的分子扩散是整个液膜传质过程的速率控制段.这一结论将导致对液膜结构更加深刻的理解,并将有助于液膜体系的改进.     

液膜法提取分离对氨基苯甲酸的研究

由磷酸三丁酯(TBP)、表面活性剂和煤油为油相,氢氧化钠溶液为内水相,含对氨基苯甲酸(PABA)的水溶液为料液(外水相),组成了W/O/W型乳状液膜体系,用乳状液膜法对料液中的PABA进行了分离富集研究。探讨了PA-BA在水中的形态分布及其液膜分离的传质机理,考察了表面活性剂种类、TBP质量分数浓度、外水相pH值和内水相氢氧化钠浓度等因素,对PABA传质分离的影响。结果表明,采用适宜的乳状液膜体系,在最佳的操作条件下,对含PABA浓度为500 mol/L的料液进行分离富集时,仅经一级液膜分离过程,PABA的分离提取率可达99%。     

乳状液膜法处理三氯乙醛废水的研究

本工作是用乳状液膜法处理三氯乙醛废水的初步实验.实验系将氢氧化钠水溶液包以煤油作为液膜,处理含有50—200ppm的三氯乙醛水溶液.实验考察了影响三氯乙醛渗透的一些因素,在适当的条件下可以脱除95%以上的三氯乙醛.并计算了该液膜体系的总包传质系数,结果表明它趋向于一个恒定值.     

液膜法脱除废水中的氰化物

本文用聚胺E644作乳化剂,研究了用内相包裹NaOH 水溶液的W/O 型乳状液脱除废水中氰化物的方法。讨论了影响液膜稳定性、液膜传质速率等的因素.表面活性剂浓度、油内比、乳水比、温度及搅拌速度对液膜的稳定性及液膜传质速率均有不同程度的影响。确认本系统中氰化物的迁移属Ⅰ型促进传递机理。本文还导出了同时考虑外相边界层及膜相传质阻力的固定液滴——渐进前沿模型。采用摄动法求得了该模型的零级近似解。模型计算值与实验值能很好地符合。     

乳状液膜分离稀土的传质模型的发展现状

本文对近些年出现的乳状液膜法迁移稀土离子的传质模型作了较为详细的总结和比较。由于在液膜体系中，影响迁移的因素比较多，推导出的数学模型都比较复杂。经过简化和近似处理后得到的解析式，都可以和实验值取得较好的一致性，但又有一定的局限性，另外，新的液膜体系不断出现，因此对数学模型的研究仍需深入。     

改良型湿壁塔液膜传质特性与端末效应的研究

本文采用疋田晴夫等提出的改良型湿壁塔作为建立研究传质的基础实验装置.测定了液膜厚度沿壁的分布,实验结果表明膜厚的实验值与理论值吻合较好;又选用CO_2-H_2O系统对塔的液膜传质特性进行了研究,并提出了液膜传质系数的无因次准数关联式;实验结果与渗透理论计算值比较,获得了良好的一致性.研究还表明通过简单地操作控制即能消除由端末效应引起的偏差.因此改良型湿壁塔是进行气液传质研究的良好装置.     

旋转填充床中伴有可逆反应的气液传质

应用CO2-MDEA气液吸收体系,对旋转填充床中伴有可逆反应的气液传质过程进行了定量的模型研究。在所有反应都可逆的情况下,根据Higbie渗透理论建立了旋转床中CO2-MDEA体系的扩散-反应传质模型。通过模型对传质过程的定量描述以及实验结果对模型的验证,超重力旋转床的强化作用可进一步被揭示为:由于不断更新的液膜使得可溶性气体在液膜内形成较大的浓度梯度,从而极大地增大了传质系数,强化了传质;旋转床的强化作用是在动态的传质过程中完成的,液膜的寿命越短则传质系数越大。在不同转速、温度、MDEA浓度和气液流量条件下进行了实验,本文模型的模拟值和实验结果吻合较好。     

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。     

乳状液膜法提取分离水中苯胺

采用非流动载体乳状液膜体系对水中苯胺的提取进行了研究.考察了影响苯胺传质的几种因素：内水相盐酸浓度、外水相pH值、表面活性剂种类和浓度、乳水比等.结果表明,在适宜的操作条件下,当水中苯胺浓度为500 mg·L^-1时,经过一级液膜处理,水中苯胺的含量可降到1.5 mg·L^-1.另外初步探讨了表面活性剂的结构和性质对膜相黏度、界面黏度、稳定性和苯胺传质速率的影响.     

乳状液膜提取青霉素及其溶胀的研究

采用W／O型乳状液膜提取模拟发酵液中的青霉素,考察膜相添加剂、表面活性剂、载体、解析剂Na2CO3浓度、搅拌速度对青霉素传质和液膜溶胀的影响。以span80为表面活性剂、三辛胺为流动载体、液体石蜡为膜相添加剂、煤油为膜溶剂组成的乳状液膜体系。结果表明：青霉素提取率随表面活性剂和载体浓度的增加而明显增加。但表面活性剂浓度增加使液膜易产生再乳化,而再乳化和搅拌是夹带溶胀产生的主要原因;水的渗透(渗透溶胀)随载体和内相NaCO3浓度升高而增加。液膜溶胀是影响液膜技术工业化应用的关键因素之一。适宜的液膜配方和操作条件,有利于控制液膜溶胀,增加青霉素的提取率。在本研究中,青霉素的提取率最高可达91．5％,液膜溶胀率为16％。     

THE STUDY ON THE MASS TRANSFER MECHANISM OF EUROPIUM ION THROUGH LIQUID SURFACTANT MEMBRANES

The transfer of trivalent europium ion in a liquid surfactant membrane system is investigated in order toclarify the characteristics of liquid membrane separation process and the availability of this technique forrecovering trivalent lanthanides and actinides.A layered structure model for the emulsion globule is sug-gested.The equations describing the relationship among the effective membrane thickness,the time andother factors are derived and verified experimentally.Results show that under certain conditions the decreas-ing concentration of europium ion in the external phase is proportional to the square root of the time,the acidity of the internal phase and the carrier concentration in the membrane phase.The membrane phase consists of kerosene(solvent),Span-80(surfactant)and di-(2-ethylhexyl) phosphoricacid(HDEHP,carrier).The internal phase is dilute nitric acid and the external phase is aqueous solu-tion containing Eu(NO_3)_3.The mass transfer rate of europium in this system is high and the recovery ofeuropium may be more than 99%.     

乳状液膜法提取苯丙氨酸的研究

本文采用以Ｐ２０４为载体，Ｓｐａｎ８０为表面活性剂，煤油为溶剂，ＨＣｌ为内 解析剂，氨基酸料液为外水相的液膜体系，在适宜的酸度下，以Ｈ＾＋浓度差的推动力，对苯丙氨酸在液膜体系中的迁移行为进行了研究，讨论了其迁移机理，确定了提取苯丙氨酸的适宜条件，撮率可达８０５以上，并探讨了工业应用液膜法从氨基酸发酵液中提取氨基酸的可行性。     

Mathematical modeling of penicillin G Extraction by a bifunctional surfactant in a continuous extraction column

A bifunctional surfactant was used as a carrier of penicillin G for its continuous extraction by an emulsion liquid membrane without an extradant in a countercurrent extraction column of Oldshue-Rushton type. A permeation model was presented to describe transport mechanism of penicillin G in the continuous extraction system, including an axial dispersion model for the continuous phase and a mass transfer model for the dispersed emulsion phase. The mass transfer model describes the external mass transfer around the emulsion drop, the reaction at the external interface, the diffusion as well as the reaction equilibrium within the w/o emulsion drop, and the pH change of internal aqueous phase. Here, we considered three experimental variables: penicillin G concentration, pH of continuous phase and surfactant concentration. The calculated results from the permeation model fitted the experimental data well. This paper is dedicated to Dr. Youn Yong Lee on the occasion of his retirement from Korea Institute of Science and Technology.     

Solvent Extraction of Europium with Diisostearylphosphoric Acid and Its Application to an Emulsion Liquid Membrane Technique

Abstract

The extraction equilibrium of europium (Eu) with diisostearylphosphoric acid (DISPA, HR) was measured in various solvents at 303 K. The stoichiometry of the complex extracted and the extraction equilibrium constants were determined. The extraction rate of Eu with DISPA was measured using a stirred transfer cell. The extraction rate was found to be limited by the diffusion process. The permeation of Eu through an emulsion liquid membrane containing DISPA as a carrier and Span 80 as a surfactant was carried out. Under the experimental conditions, the reaction resistance contributed to the overall permeation process. An interfacial reaction model was proposed to explain the experimental results.     

Interfacial Mass Transfer in Ligand Accelerated Metal Extraction by Liquid Surfactant Membranes

Abstract

Interfacial mass transfer rates were determined for the extraction of Co(II), Ni(II), and Cu(II) by di-(2-ethyl hexyl) phosphoric acid by using a modified Lewis cell. This allowed us to elucidate the effect of ligands on liquid surfactant membrane extraction of heavy metal ions by ligand addition to the external aqueous phase. The effects of different ligands on the kinetics of extraction and the influence of surfactant on interfacial resistance to mass transfer were then examined.     

液膜对不同酸度磷矿浸出液中稀土的提取

用浓盐酸溶解富含镧、铈等稀土离子的织金磷矿,得到含稀土离子的磷矿浸出液,以P204为载体、Span80或T154作表面活性剂、磺化煤油作溶剂、盐酸作内水相解析剂制成的乳状液膜对酸解液中镧、铈等稀土离子进行提取,考察了流动载体浓度、表面活性剂种类及浓度对稀土提取率的影响及磷矿浸出液中不同浓度稀土离子在不同酸度下的分离提取情况. 结果表明,液膜中最佳载体浓度为12%(j),最佳表面活性剂浓度为4%(j),随外水相pH值增大,液膜对稀土离子的提取率提高,外水相稀土离子浓度为100 mg/L,pH=1时,其提取率可达79.93%.     

Transport of Europium(III) through Supported Liquid Membrane Containing Diisodecylphosphoric Acid

Abstract

Carrier mediated transport of europium has been investigated by the use of a flat-sheet membrane impregnated with diisodecylphosphoric acid (DIDPA). The addition of 1-octanol to the membrane improves the stripping process, and hence europium can be quantitatively transported from the feed solution of 0.1 M HNO₃ into the product solution of 5 M HNO₃. Its concentration in the feed solution decreases as [Eu] _f,t = [Eu] _f,0 exp (-k _obs t). The apparent rate constant (k _obs) increases with increasing carrier concentration and becomes nearly constant above 0.05 M DIDPA The europium flux is proportional to initial europium concentrations less than 10^?3 M, and becomes constant at high concentrations.     

Zinc and Copper Separation through an Emulsion Liquid Membrane Containing Di‐(2‐Ethylhexyl) Phosphoric Acid as a Carrier

The separation of zinc and copper ions from sulfuric acid solutions by an emulsion liquid membrane (ELM), using di‐(2‐ethylhexyl) phosphoric acid (D2EHPA) as a carrier, has been investigated. The batch extraction of zinc and copper was carried out while varying a selection of experimental conditions, i.e., stirring speed, treatment ratio, concentrations of metal ions in the feed phase, carrier and Span 80 concentration in the membrane, and internal phase concentration. The results obtained demonstrate the effectiveness of D2EHPA as a carrier for the separation of zinc and copper from sulfuric acid media using an ELM. An increase of the D2EHPA concentration beyond 2 vol.‐% does not result in the improved extraction of zinc because the viscosities of the membrane and emulsion have a trend to increase for higher carrier concentrations. It was found that the extraction rate of copper was affected by the carrier concentration in the liquid membrane and by the pH and metal content in the external phase. A 3 vol.‐% concentration of surfactant in the organic phase was required to stabilize the emulsion. The number of stages required for the extraction of zinc and copper by an ELM was determined from McCabe‐Thiele plots.     

Novel Diglycolamic Acid Functionalized Iron Oxide Particles for the Mutual Separation of Eu(III) and Am(III)

Iron oxide (Fe₃O₄) particles functionalized with diglycolamic acid (Fe-DGAH) were synthesized and characterized by TG-DTA, X-Ray diffraction,¹H NMR, and scanning electron microscopy (SEM). The extraction behavior of Am(III) and Eu(III) in Fe-DGAH was studied from dilute nitric acid medium to examine the feasibility for the mutual separation of trivalent actinides and lanthanides using Fe-DGAH. For this purpose, the effect of various parameters such as the duration of equilibration and concentrations of europium, nitric acid, and diethylenetriaminepentaacetic acid (DTPA) in the aqueous phase on the distribution ratio (K_d) of Am(III) and Eu(III) was studied. The conditions needed for the efficient separation of Am(III) from Eu(III) were optimized using DTPA. The distribution ratio of ?10⁴ mL/g was obtained for both Am(III) and Eu(III) at pH 3, and it decreased with an increase in the concentration of nitric acid. However, a separation factor of Eu(III) over Am(III) of ?150 was achieved in the presence of DTPA. Rapid sorption of metal ions in the initial stages of equilibration followed by the establishment of equilibrium occurred within 2 h. The sorption data were fitted to the Langmuir adsorption model, and the apparent europium sorption capacity was determined to be ?50 mg/g. The study indicated the feasibility of using Fe-DGAH particles for magnetic separation of Eu(III) from Am(III) with high separation factors.