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Concentration techniques

Techniques, such as spectroscopy (Chapter 10), potentiometry (Chapter 11), and voltammetry (Chapter 11), in which the signal is proportional to the relative amount of analyte in a sample are called concentration techniques. Since most concentration techniques rely on measuring an optical or electrical signal, they also are known as instrumental techniques. For a concentration technique, the relationship between the signal and the analyte is a theoretical function that depends on experimental conditions and the instrumentation used to measure the signal. For this reason the value of k in equation 3.2 must be determined experimentally. [Pg.38]

Every discipline has its own terminology. Your success in studying analytical chemistry will improve if you master the language used by analytical chemists. Be sure that you understand the difference between an analyte and its matrix, a technique and a method, a procedure and a protocol, and a total analysis technique and a concentration technique. [Pg.50]

For a concentration technique the relationship between the measured signal and an analyte s concentration is given by equation 4.5... [Pg.67]

This analysis is an example of a concentration technique. Once the original sample is brought to volume in the 100-mL volumetric flask, any portion of the sample solution, even that obtained on filtering, may be used for the analysis. [Pg.527]

Quantitative mass spectrometry, also used for pharmaceutical appHcations, involves the use of isotopicaHy labeled internal standards for method calibration and the calculation of percent recoveries (9). Maximum sensitivity is obtained when the mass spectrometer is set to monitor only a few ions, which are characteristic of the target compounds to be quantified, a procedure known as the selected ion monitoring mode (sim). When chlorinated species are to be detected, then two ions from the isotopic envelope can be monitored, and confirmation of the target compound can be based not only on the gc retention time and the mass, but on the ratio of the two ion abundances being close to the theoretically expected value. The spectrometer cycles through the ions in the shortest possible time. This avoids compromising the chromatographic resolution of the gc, because even after extraction the sample contains many compounds in addition to the analyte. To increase sensitivity, some methods use sample concentration techniques. [Pg.548]

ON-LINE CONCENTRATION TECHNIQUES IN MICELLE ELECTROKINETIC CHROMATOGRAPHY (MEKC)... [Pg.250]

Under similar reaction-conditions, the vanadium species V(N2)6 (139) has been isolated. In addition, a species V2(Na) (n probably = 12) was observed (139). The metal nuclearity was established by the standard, metal-concentration techniques. A comparison of the optical spectra of V(N2) and V(CO)e 128) suggested that these molecules have very similar, electronic properties, and the data clearly established that N2 is a strong, field ligand in its bonding properties. Interestingly, atomic V could be isolated in N2 matrices from 8- 12K co-... [Pg.141]

Isolation and Concentration Techniques Using Physical Methods.739... [Pg.883]

ISOLATION AMD CONCENTRATION TECHNIQUES USING SOLVENT EXTRACTION... [Pg.891]

Clearly, one option to reduce the add-on is to use high-efficiency size formulations. However, there is a limit to what can be achieved by this approach. Even if the add-on is reduced to only 5%, the pollution load is still substantial. The two main options to facilitate disposal are (a) recovery of size polymers and (b) biological effluent treatment. Recovery of size polymers, particularly from water-soluble synthetic sizes, is based on extraction washing using the minimum quantity of water. Recovery rates in the region of 50% have been quoted for polyfvinyl alcohol) and carboxymethylcellulose size formulations. It is necessary to apply one of three concentration techniques precipitation, condensation or ultrafiltration [205]. [Pg.110]

The Baermann concentration technique has greater sensitivity for the detection of strongyloides larvae than do the standard concentration techniques described above. This technique is useful clinically for the diagnosis and monitoring of therapy of strongyloides infections, and it is useful epidemiologically for the examination of soil for the larvae of nematode parasites. [Pg.16]

Cytocentrifugation is used to prepare additional non-gynecologic specimens containing little or nonvisible sediment after centrifugation. This method is used in addition to the monolayer concentration technique for immunohisto-chemistry staining. [Pg.407]

Lieser et al. [628] studied the application of neutron activation analysis to the determination of trace elements in seawater, with particular reference to the limits of detection and reproducibility obtained for different elements when comparing various preliminary concentration techniques such as adsorption on charcoal, cellulose, and quartz, and complexing agents such as dithizone and sodium diethyldithiocarbamate. [Pg.284]

Another concentration technique similar in principle to supercritical fluid chromatography, SFC (p. [Pg.505]

In some cases, confirming identification of components obtained from soil, such as pesticides, is essential. Thus, the uncertainty in some analyses needs to be addressed. This can be accomplished by identifying the components using two entirely different methods such as IR spectroscopy and MS. Although GC-IR-MS methods can positively identify separated components, the IR component of the system is not nearly as sensitive as are the GC and MS components. This detracts from the usefulness of this method. However, in cases where the level of analyte is not limiting, which frequently occurs in soil extracts, this can be an excellent method to use. Also, with modern concentration techniques, it is neither difficult nor time-consuming to concentrate analytes to a level that is identifiable by IR spectroscopy [17,18],... [Pg.332]

A great number of separation processes are based on solvent extraction, especially since this is also a concentration technique. For these reasons, solvent extraction will be considered, both from the point of view of the sampling process and from that of the general analytical process. Solvent extraction is ultimately a process of partitioning between two immiscible solvents, and for its optimization it is necessary to know first of all the operational parameters of the system. [Pg.437]

Effective concentrated technique Effective removal technique Effective removal technique Not applicable... [Pg.251]

For most odour nuisance problems, chemical plants, refineries, livestock production, food processing, rendering, water purification plants etc., the compounds responsible for the odour are known. So chemical analysis of the odour can be limited to these odorants, and selective concentrating techniques can be used. Selective concentrating methods are based on specific absorption techniques, using particular chemical reactions of odorant classes. Sometimes several absorption methods have to be used in order to describe the odour problem, thus increasing the labor cost of the analysis. On the other hand absorption methods allow better quantitative results. Selective absorption of odorants from air produces a far less complex mixture. We developed or are developing several of these methods for aldehydes, amines, acids, thiols etc. [Pg.167]

Electrophoretic concentration techniques are based on the difference in mobility of an analyte in two separate zones, mainly due to differences in electric field strength between the zones.The main advantage of this type of concentration is that no modification of the basic instrument is required. [Pg.338]


See other pages where Concentration techniques is mentioned: [Pg.38]    [Pg.50]    [Pg.770]    [Pg.276]    [Pg.411]    [Pg.232]    [Pg.593]    [Pg.885]    [Pg.168]    [Pg.127]    [Pg.131]    [Pg.505]    [Pg.358]    [Pg.363]    [Pg.110]    [Pg.25]    [Pg.215]    [Pg.367]    [Pg.500]    [Pg.92]    [Pg.167]    [Pg.244]    [Pg.249]    [Pg.338]   
See also in sourсe #XX -- [ Pg.163 , Pg.164 , Pg.165 , Pg.166 , Pg.167 , Pg.168 , Pg.169 , Pg.170 , Pg.171 , Pg.172 , Pg.173 , Pg.174 , Pg.175 , Pg.176 , Pg.177 ]

See also in sourсe #XX -- [ Pg.124 ]




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