Solvent extraction multiple extractions

Marinsky, J. A. and Y. Marcus, eds.. Ion Exchange and Solvent Extraction, multiple volumes (New York Marcel-Dekker, 1966 and subsequent). 

Solvent Extraction. With solvent extraction, organics are separated from a waste by mixing the waste with a solvent capable of dissolving or extracting the organics. The extraction process can have multiple stages and be operated where the solvent and waste pass concurrently or countercurrenfly. 

Co (I I) complex formation is the essential part of copper wet analysis. The latter involves several chemical unit operations. In a concrete example, eight such operations were combined - two-phase formation, mixing, chelating reaction, solvent extraction, phase separation, three-phase formation, decomposition of co-existing metal chelates and removal of these chelates and reagents [28]. Accordingly, Co (I I) complex formation serves as a test reaction to perform multiple unit operations on one chip, i.e. as a chemical investigation to validate the Lab-on-a-Chip concept. 

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. 

Sample preparation techniques vary depending on the analyte and the matrix. An advantage of immunoassays is that less sample preparation is often needed prior to analysis. Because the ELISA is conducted in an aqueous system, aqueous samples such as groundwater may be analyzed directly in the immunoassay or following dilution in a buffer solution. For soil, plant material or complex water samples (e.g., sewage effluent), the analyte must be extracted from the matrix. The extraction method must meet performance criteria such as recovery, reproducibility and ruggedness, and ultimately the analyte must be in a solution that is aqueous or in a water-miscible solvent. For chemical analytes such as pesticides, a simple extraction with methanol may be suitable. At the other extreme, multiple extractions, column cleanup and finally solvent exchange may be necessary to extract the analyte into a solution that is free of matrix interference. 

Solvent Extraction Aqueous sample is partitioned with an immiscible organic solvent. Extraction efficiency depends on the affinity of the solute for the organic solvent. All sample types Samples with a high affinity for water are not extracted. Extractions can be performed by a simple single equilibration or by multiple equilibrations with fresh solvent. Solvent impurities concentrated along with sample. 

Chromatographic procedures applied to the identification of proteinaceous paint binders tend to be rather detailed consisting of multiple analytical steps ranging from solvent extractions, chromatography clean up, hydrolysis, derivatisation reactions, and measurement to data analysis. Knowledge of the error introduced at each step is necessary to minimise cumulative uncertainty. Reliable results are consequently obtained when laboratory and field blanks are carefully characterised. Additionally, due to the small amounts of analyte and the high sensitivity of the analysis, the instrument itself must be routinely calibrated with amino acid standards along with measurements of certified reference proteins. All of these factors must be taken into account because many times there is only one chance to take the measurement. 

Automation CL measurements can be performed very rapidly and with minimal human participation if the flow system is carefully designed. Several reagents can be added to the sample if multiple flow lines are used and at predetermined times to fulfill the best condition for maximum CL sensitivity. Introduction of special devices into the flow line, which allow procedures otherwise time-consuming such as solvent extraction or ion exchange, improve substantially the sensitivity and selectivity of the technique. 

A 50 per cent solution of solute C in solvent A is extracted with a second solvent B in a countercurrent multiple contact extraction unit. The mass of B is 25 per cent that of the feed solution, and the equilibrium data are ... 

Nowicki et al. [51] point out that in the development of a Soxhlet sample preparation technique for sediment samples, the empty paper Soxhlet thimbles contained organic contaminants which adversely affected results. Glass thimbles were tried and found to be satisfactory. The authors detail the identification of organics solvent-extracted from paper and glass Soxhlet thimbles, and discuss the stability for multiple use of the two materials for trace organic sample preparation. 

Samples containing heavy oil, along with the volatile components can severely contaminate pnrge-and-trap instrumentation, and caution is advised when interpreting the data. For such samples it may be advisable to use a separatory funnel for the water extraction method for semivolatiles (EPA 3520). In this method, the sample is ponred into a funnel-shaped piece of glassware, solvent is added, and the mixtnre is shaken vigorously. After layer separation, the extract (i.e., the solvent layer) is removed. Altered, dried with a desiccant, and concentrated. Multiple extractions on the same sample may increase overall recovery. 

Solvent extraction reduction is most frequently performed mainly in connection with the extraction of solid and biological samples by liquid partition. Extractions are typically accomplished using a Soxhlet apparatus that provides the benefits of multiple extractions. By repeated distillation and condensation of the solvent, the apparatus allows multiple extractions using the same (small) volume of solvent. Soxhlet extraction has been a standard method for many decades, and it is often the method against which other extraction methods are measured and verified [14]. 

An example of a schematic for sample treatment, extraction, and separation procedures is given in Simoneit, and it follows the method first used by Simoneit and Mazurek with minor modifications for data comparison purposes. The samples are powdered and dried, then typically extracted using ultrasonic agitation multiple times with a mixture of dichloromethane (CH2CI2) and methanol (3 1 v/v). The solvent extracts are filtered through an annealed glass fiber filter for the removal of insoluble particles, concentrated by rotary evaporation and then by a stream of filtered nitrogen gas. 

In multiple extraction of solute from aqueous to organic phase, if the volume of the organic solvent used each time remains constant and equal to the volume of aqueous phase, the weight unextracted after n such operations is ... 

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