Liquid extracts substances

Liquid-liquid extraction is a process for separating components in solution by their distribution between two immiscible liquid phases. Such a process can also be simply referred to as liquid extraction or solvent extraction however, the latter term may be confusing because it also applies to the leaching of a soluble substance from a solid. 

Application of rotating coiled columns has become attractive for preparative-scale separations of various substances from different samples (natural products, food and environmental samples) due to advantages over traditional liquid-liquid extraction methods and other chromatographic techniques. The studies mainly made during the last fifteen years have shown that using rotating coiled columns is also promising for analytical chemistry, particularly for the extraction, separation and pre-concentration of substances to be determined (analytes) before their on-line or off-line analysis by different determination techniques. 

Wc have seen that molecular substances tend to have low melting points, while network, ionic, and metallic substances tend to have high melting points. Therefore, with a few exceptions, such as mercury, a substance that is liquid at room temperature is likely to he a molecular substance. Liquid solvents are heavily used in industry to extract substances from natural products and ro promote the synthesis of desired compounds. Because many of these solvents have high vapor pressures and so give off hazardous fumes, luinids that have low vapor pressures hut dissolve... 

Liquid-liquid extraction (also called solvent extraction) is the transfer of a substance (a consolute) dissolved in one liquid to a second liquid (the solvent) that is immiscible with the first liquid or miscible to a very limited degree. This operation is commonly used in fine chemicals manufacture (I) to wash out impurities from a contaminated solution to a solvent in order to obtain a pure solution (raffinate) from which the pure substance will be isolated, and (2) to pull out a desired substance from a contaminated liquid into the solvent leaving impurities in the first liquid. The former operation is typically employed when an organic phase is to be depleted from impurities which are soluble in acidic, alkaline, or neutral aqueous solutions Water or a diluted aqueous solution is then used as the solvent. The pure raffinate is then appropriately processed (e.g. by distillation) to isolate the desired consolute. In the latter version of extraction impurities remain in the first phase. The extract that has become rich in the desired consolute is then appropriately processed to isolate the consolute. Extraction can also be used to fractionate multiple consolutes. 

Grade extracts of different plants are often rich in lipophilic substances, such as plant oils, chlorophylls, and waxes and also highly polar components such as tannines or sugars. Because the complicated liquid-liquid extraction (LLE) procedures are... 

There are basically three methods of liquid sampling in GC direct sampling, solid-phase extraction and liquid extraction. The traditional method of treating liquid samples prior to GC injection is liquid-liquid extraction (LLE), but several alternative methods, which reduce or eliminate the use of solvents, are preferred nowadays, such as static and dynamic headspace (DHS) for volatile compounds and supercritical fluid extraction (SFE) and solid-phase extraction (SPE) for semivolatiles. The method chosen depends on concentration and nature of the substances of interest that are present in the liquid. Direct sampling is used when the substances to be assayed are major components of the liquid. The other two extraction procedures are used when the pertinent solutes are present in very low concentration. Modem automated on-line SPE-GC-MS is configured either for at-column conditions or rapid large-volume injection (RLVI). 

Solvent extraction, also called liquid-liquid extraction, can be used to separate a substance from a solution by extraction into another solvent. It can be used ether to recover a valuable substance from the original solution, or to purify the original solvent by removing an unwanted component. Examples of solvent extraction are the extraction of uranium and plutonium salts from solution in nitric acid, in the nuclear industry and the purification of water. 

Leoni [366] observed that in the extraction preconcentration of organochlo-rine insecticides and PCB s from surface and coastal waters in the presence of other pollutants such as oil, surface active substances, etc., the results obtained with an absorption column of Tenax-Celite are equivalent to those obtained with the continuous liquid-liquid extraction technique. For non-saline waters that contain solids in suspension that absorb pesticides, it may be necessary to filter the water before extraction with Tenax and then to extract the suspended solids separately. Analyses of river and estuarine sea waters, filtered before extraction, showed the effectiveness of Tenax, and the extracts obtained for pesticide analysis prove to be much less contaminated by interfering substances than corresponding extracts obtained by the liquid-liquid technique. Leoni et al. [365] showed that for the extraction of organic micro pollutants such as pesticides and aromatic polycyclic hydrocarbons from waters, the recoveries of these substances from unpolluted waters (mineral and potable waters) when added at the level of 1 xg/l averaged 90%. 

Solvent extraction, sometimes called liquid-liquid extraction, involves the selective transfer of a substance from one liquid phase to another. Usually, an aqueous solution of the sample is extracted with an immiscible organic solvent. For example, if an aqueous solution of iodine and sodium chloride is shaken with carbon tetrachloride, and the liquids allowed to separate, most of the iodine will be transferred to the carbon tetrachloride layer, whilst the sodium chloride will remain in the aqueous layer. The extraction of a solute in this manner is governed by the Nernstpartition or distribution law which states that at equilibrium, a given solute will always be distributed between two essentially immiscible liquids in the same proportions. Thus, for solute A distributing between an aqueous and an organic solvent,... 

Liquid-Liquid extraction is a versatile and dependable separation technique wherein an aqueous solution is usually brought into contact with another organic solvent, exclusively immiscible with the former, so as to affect a legitimate and actual transfer of either one or more solutes into the latter. The normal-feasible separations which can thus be achieved are found to be rather easy, fast, convenient and effective resonably. Invariably such separations may be performed by shaking the two liquids in a separatory funnel for a few minutes and may be extended either to large quantities of pharmaceutical substances or trace levels. 

The previous chapters have demonstrated that liquid-liquid extraction is a mass transfer unit operation involving two liquid phases, the raffinate and the extract phase, which have very small mutual solubihty. Let us assume that the raffinate phase is wastewater from a coke plant polluted with phenol. To separate the phenol from the water, there must be close contact with the extract phase, toluene in this case. Water and toluene are not mutually soluble, but toluene is a better solvent for phenol and can extract it from water. Thus, toluene and phenol together are the extract phase. If the solvent reacts with the extracted substance during the extraction, the whole process is called reactive extraction. The reaction is usually used to alter the properties of inorganic cations and anions so they can be extracted from an aqueous solution into the nonpolar organic phase. The mechanisms for these reactions involve ion pah-formation, solvation of an ionic compound, or formation of covalent metal-extractant complexes (see Chapters 3 and 4). Often formation of these new species is a slow process and, in many cases, it is not possible to use columns for this type of extraction mixer-settlers are used instead (Chapter 8). 

In an optimisation procedure involving the minimal partition coefficient, the minimal partition coefficient is calculated using all compositions of the extraction liquid (all possible combinations of x, X2 and within the mixture space). The highest value calculated for this minimal partition coefficient (the maximal minimal partition coefficient) is the optimal value and hence the composition where the partition coefficient of the worst extractable substance is highest. 

Extraction efficiency. Recovery of the analyte from biological matrix after sample pretreatment (i.e., liquid-liquid extraction, solid-phase extraction, protein precipitation, etc.) to remove endogenous substances. 

Like all the mass transfer operations, liquid extraction is a means of separating the components of a solution, and it is accomplished by bringing the solution into contact with another insoluble phase. The unequal distribution of the components of the solution between the two phases which then results provides the separation. In the case of liquid extraction, of course, the two phases in question are both liquids, but, just as in the other mass transfer operations, intimacy of contact and large interfacial area between the phases are required for rapid diffusional transfer of substance from one phase to the other. 

Conditions sometimes exist that may make separations by distillation difficult or impractical or may require special techniques. Natural products such as petroleum or products derived from vegetable or animal matter are mixtures of very many chemically unidentified substances. Thermal instability sometimes is a problem. In other cases, vapor-liquid phase equilibria are unfavorable. It is true that distillations have been practiced successfully in some natural product industries, notably petroleum, long before a scientific basis was established, but the designs based on empirical rules are being improved by modern calculation techniques. Even unfavorable vapor-liquid equilibria sometimes can be ameliorated by changes of operating conditions or by chemical additives. Still, it must be recognized that there may be superior separation techniques in some cases, for instance, crystallization, liquid-liquid extraction, supercritical extraction, foam fractionation, dialysis, reverse osmosis, membrane separation, and others. The special distillations exemplified in this section are petroleum, azeotropic, extractive, and molecular distillations. 

One important analytical use of liquid—liquid extraction is to achieve a desired degree of concentration of a desired material. Conversely it can be used to reduce the concentration of an unwanted, interfering substance to a suitable low value. 

In liquid-liquid extraction one or more components are removed from a liquid mixture by intimate contact with a second liquid that is itself nearly insoluble in the first liquid and dissolves the impurities and not the substance that is to be purified. In other cases, the second liquid may dissolve i.e., extract from the first liquid, the component that is to be purified, and leave associated impurities in die first liquid. Liquid-liquid extraction may be earned out by simply mixing die two liquids widi agitation and dien allowing diem to separate by standing. It is often economical to use counter-current extraction, in which the two immiscible liquids are caused to flow past or dirough one another in opposite directions. Thus fine droplets of heavier liquid can be caused to pass downward through the higher liquid in a vertical tube or tower,... 

Determination of the tannin. The solution of the substance for this determination may be made like those already indicated (see above, section 3), but should be more dilute, so that 10 c.c. of it reduce 4-10 c.c. of permanganate about 5 grams of a solid extract, 10 grams of a liquid extract or of a rich material like sumac, or 20 grams of an ordinary bark are taken per litre of solution. The liquid is filtered if necessary. 

Moisture.—5 grams of the substance are dried (after evaporation in the case of a liquid extract) at 105° to constant weight. 

Good bgwood extract usually contains 40-45% of water if liquid or 9-12% if solid it should not contain added extraneous substances, especially sugar or low products in the dry extracts or molasses in the liquid extracts. In genuine extracts there is no saccharose and the alkalinity of the ash varies from 0 4 to 0 5 gram (expressed as potassium carbonate) per 100 grams of dry matter. 

Extraction. A system has been devised which allows for performing successive liquid-liquid extractions followed by reagent addition and color formation. In one application the test substance in water, after being extracted into another solvent, is backwashed with color-forming reagent, and the solution is then passed into the colorimeter for reading and recording. 

---