Interfering

Interfering signals in remote field eddy currents... 

The instrument prevents automatically from interfering factors. 

Fig. 11 shows a composite model of the wave at U X =0.25. In the interfering wave on the upper and lower part of the insert metal, (a) is the same phase, and (b) is the opposite phase. A composite wave is attenuated by the weakened interference as the same phase, and is amplified by the strengthened interference as the opposite phase. 

In high-energy physics experiments there can be many interfering events superimposed on the events of interest. An example is the detection of gamma rays in the presence of high-energy electrons and protons. The... 

Voimer M, Stratmann M and Viefhaus FI 1990 Eleotroohemioal and eleotron speotrosoopio investigations of iron surfaoes modified with thiols Surf. Interf. Anal. 16 278-82... 

Sulphur, as sulphide ion, is detected by precipitation as black lead sulphide with lead acetate solution and acetic acid or with sodium plumbite solution (an alkaLine solution of lead acetate). Halogens are detected as the characteristic silver halides by the addition of silver nitrate solution and dilute nitric acid the interfering influence of sulphide and cyanide ions in the latter tests are discussed under the individual elements. 

The most common interfering substance, especially with alcohols of low mole cular weight, is water this may result in an inaccurate interpretation of the test if applied alone. Most of the water may usually be removed by shaking with a little anhydrous calcium sulphate,. though dry ethers (and also the saturated aliphatic and the simple aromatic hydrocarbons) do not react with sodium, many other classes of organic compounds do. Thus ... 

The physical implications of the commutation of two operators are very important because they have to do with what pairs of measurements can be made without interfering with one another. For example, the fact that the x coordinate operator x= x and its... 

One of the most widely used techniques for preventing an interference is to bind the interferent as a soluble complex, preventing it from interfering in the analyte s determination. This process is known as masking. Technically, masking is not a separation... 

Two frequently encountered analytical problems are (1) the presence of matrix components interfering with the analysis of the analyte and (2) the presence of analytes at concentrations too small to analyze accurately. We have seen how a separation can be used to solve the former problem. Interestingly, separation techniques can often be used to solve the second problem as well. For separations in which a complete recovery of the analyte is desired, it may be possible to transfer the analyte in a manner that increases its concentration. This step in an analytical procedure is known as a preconcentration. 

A coprecipitated impurity in which the interfering ion occupies a lattice site in the precipitate. 

Occlusions, which are a second type of coprecipitated impurity, occur when physically adsorbed interfering ions become trapped within the growing precipitate. Occlusions form in two ways. The most common mechanism occurs when physically adsorbed ions are surrounded by additional precipitate before they can be desorbed or displaced (see Figure 8.4a). In this case the precipitate s mass is always greater than expected. Occlusions also form when rapid precipitation traps a pocket of solution within the growing precipitate (Figure 8.4b). Since the trapped solution contains dissolved solids, the precipitate s mass normally increases. The mass of the precipitate may be less than expected, however, if the occluded material consists primarily of the analyte in a lower-molecular-weight form from that of the precipitate. 

Selectivity As described earlier, most ion-selective electrodes respond to more than one analyte. For many ion-selective electrodes, however, the selectivity for the analyte is significantly greater than for most interfering ions. Published selectivity coefficients for ion-selective electrodes (representative values are found in Tables 11.1 through 11.3) provide a useful guide in helping the analyst determine whether a potentiometric analysis is feasible for a given sample. 

In this manner, a current efficiency of 100% is maintained. Furthermore, since the concentration of Ce + remains at its initial level, the potential of the working electrode remains constant as long as any Fe + is present. This prevents other oxidation reactions, such as that for liiO, from interfering with the analysis. A species, such as Ce +, which is used to maintain 100% current efficiency, is called a mediator. 

Although cold plasmas have benefits in removing interfering ions such as ArO+, they are not necessary for other applications where interferences are not a problem. Thus, in laboratories where a range of isotopes needs to be examined, the plasma has to be changed between hot and cold conditions, whereas it is much simpler if the plasma can be run under a single set of conditions. For this reason, some workers use warm plasmas, which operate between the hot and cold conditions. 

The cold plasmas tend to be unstable, are sometimes difficult to maintain, and provide ion yields that are less than those of the hot plasmas. To obviate the difficulties of the interfering isobaric molecular ions from hot plasmas, it has been found highly beneficial to include a collision cell (hexapole see Chapter 22) before the mass analyzer itself. This collision cell contains a low pressure of hydrogen gas. lon/molecule collisions between the hydrogen and, for example, ArO+... 

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