Chemical precipitation separation method

Eor products having relatively low specific activity, such as some compounds labeled with and which are synthesized on the scale of several millimoles, classical organic chemical separation methods may be utilized, including extraction, precipitation, and crystallization. Eor separation of complex mixtures and for products having high specific activity, such as those labeled with tritium, etc, chromatographic methods utilizing paper, thin... 

However, for the past 30 years fractional separation has been the basis for most asphalt composition analysis (Fig. 10). The separation methods that have been used divide asphalt into operationally defined fractions. Four types of asphalt separation procedures are now in use ( /) chemical precipitation in which / -pentane separation of asphaltenes is foUowed by chemical precipitation of other fractions with sulfuric acid of increasing concentration (ASTM D2006) (2) solvent fractionation separation of an "asphaltene" fraction by the use of 1-butanol foUowed by dissolution of the 1-butanol solubles in... 

The standard methods of drying can be classified as deposition of the moisture as either water or ice decomposition of the water chemical precipitation absorption adsorption mechanical separation and vaporization. The completeness with which dryness can be accomplished by any process depends upon the factors controlling the equilibrium conditions achieved in the operation. A brief discussion of each method is first given. 

In view of the selective character of many colorimetric reactions, it is important to control the operational procedure so that the colour is specific for the component being determined. This may be achieved by isolating the substance by the ordinary methods of inorganic analysis double precipitation is frequently necessary to avoid errors due to occlusion and co-precipitation. Such methods of chemical separation may be tedious and lengthy and if minute quantities are under consideration, appreciable loss may occur owing to solubility, supersaturation, and peptisation effects. Use may be made of any of the following processes in order to render colour reactions specific and/or to separate the individual substances. 

Wahl and Deck were able to obtain an estimate of an assumed second-order rate coefficient ( 10 l.mole" .sec at 4°C) using a separation procedure based on the extraction of Fe(CN)e by a chloroform solution of Ph AsCl, in the presence of the ions Co(CN)g and Ru(CN)6, to reduce the exchange between the iron species in the two liquid phases. A similar estimate was obtained using a precipitation method in the presence of the carrier Ru(CN)6. A direct injection technique was used as short reaction times were necessary. Wahl has reviewed the large induced exchanges occurring in the chemical separation methods. The extraction procedure when the carriers Co(CN)6 and Ru(CN) are present provides the most satisfactory method of separation. ... 

Radiotracers are uniquely well suited to such studies. The sensitivity of detection means that only very small amounts of tracer need be added to follow the chemical pathway of the relevant species. Furthermore, it matters little what the physical or chemical state of the tracer is, for measurements may be made on liquids, solids or gases. Chromatography, solvent extraction and precipitation are amongst separation methods widely studied by means of radiotracers. In the individual separation steps the distribution of the species may be studied by simple radioactivity measurements, and subsequently the tracer will serve as a yield indicator for the overall procedure. 

Most, but not all, chemical separation methods are based on equilibrium in the sense of chemical equilibrium. Clearly, solubility is a chemical question but formation of a precipitate and filtration is a physical separation, which happens to use a favorable Ksp equilibrium... 

The lanthanide group of elements (Table 11.7) is very difficult to separate by traditional methods because of their similar chemical properties. The techniques originally used, like the precious metals, included laborious multiple fractional recrystallizations and fractional precipitation, both of which required many recycle streams to achieve reasonably pure products. Such techniques were unable to cope with the demands for significant quantities of certain pure compounds required by the electronics industry hence, other separation methods were developed. Resin ion exchange was the first of these... 

Soil washing is based on the use of water-based leachates, which are recycled continuously in the machine. The end products are a relatively clean, coarser soil fraction and a wash water containing finer soil particles and most contaminants. The small levels of organic contamination remaining in the coarser materials are removed readily with heat. The wash water, depending upon the specific contaminants, responds to various traditional treatment methods, such as bioremediation, air stripping, chemical precipitation, or membrane separation. 

Precipitation techniques used in chemical analyses also have many applications in rapid radiochemical separations. Although this method tends to have some disadvantages, such as time consumed in filtration or washing and the coprecipitation of undeslred impurities, it can still be very valuable, expecially when other rapid separation methods are not applicable. 

The RO process was implemented at the Institute of Atomic Energy, Swierk. The wastes collected there, from all users of nuclear materials in Poland, have to be processed before safe disposal. Until 1990 the wastes were treated by chemical methods that sometimes did not ensure sufficient decontamination. To reach the discharge standards the system of radioactive waste treatment was modernized. A new evaporator integrated with membrane installation replaced old technology based on chemical precipitation with sorption on inorganic sorbents. Two installations, EV and 3RO, can operate simultaneously or separately. The membrane plant is applied for initial concentration of the waste before the evaporator. It may be also used for final cleaning of the distillate, depending on actual needs. The need for additional distillate purification is necessitated due to entrainment of radionuclides with droplets or with the volatile radioactive compounds, which are carried over. 

The chemical components of the precipitate by SHCP were neither detected nor isolated by any kind of separation method, i.e., fractional precipitation, separation with a coarse filter paper, and cataphoresis. The electron microscopic observations and the X-ray diffraction analysis, and so on, disclosed an amorphous and homogeneous nature, and the chemical reactivity for various reagents was very high. The DTA suggested the formation of solid compounds at comparatively low temperature, probably during precipitation. 

Various technologies have been used to measure plasma lipids and lipoproteins and lipoprotein subfractions, including enzymatic, immunochemical, and chemical precipitation reagents, and physical methods, such as ultracentrifugation, electrophoresis, column chromatography, and others. Such methods have been reviewed extensively. As mentioned earlier, however, the cholesterol content of any particular lipoprotein class can vaiy somewhat from individual to individual. Moreover, although different methods of lipoprotein separation may produce similar lipoprotein fractions, they usually do not produce identical fractions, giving rise to systematic biases between methods that purport to measure the same component. The present discussion focuses primarily on methods and procedures commonly used in clinical practice for lipid and lipoprotein measurements. 

Table 30-1 lists a variety of separation methods that are in common use, including (1) chemical or electrolytic precipitation, (2) distillation, (3) solvent extraction, (4) ion exchange, (5) chromatography, (6) electrophoresis, and (7) field-flow fractionation. The first four are discussed in Sections 30A through 30E of this chapter. An introduction to chromatography is presented in Section 30F. Chapters 31 and 32 deal with gas and liquid chromatography, respectively, while Chapter 33 deals with electrophoresis, field-flow fractionation, and other separation methods. 

Fractionation by precipitation can be brought about by methods which are either chemical or physical in nature. Separations carried out by chemical precipitation are dealt with in the next chapter, and the present Section deals with separations by precipitation carried out by physical methods. 

Crystallization, distillation, precipitation, chemical agents, are among the other methods to be considered. No one method of separation is universally applicable the usefulness of each is related to the system to be treated and on the task to be done. With some operations there is little or no difficulty in deciding which separation method to use but not infrequently we encounter twilight situations in which any of several methods could function. Further, there are certain systems that require a suitable combination of several separate methods. 

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