Extracted in chromatography

Moreno Cordero B, Perez Pavon JL, Garda Pinto C, Fernandez Laespada E, Carabias Martinez R, and Rodriguez Gonzalo E. Analytical applications of membrane extraction in chromatography and electrophoresis. J. Chromatogr. A 2000 902 195-204. 

Approaches to modify acetate include polymer blending. No miscible polymer systems have been identified for aeetate. To improve compatibility, graft copolymer additives and cross-linking prepolymer additives have been investigated, and some potentially useful compatible blends have been identified [101 106]. Extraction of one blend component has provided voids in the aeetate fiber for holding useful additives or for gas extraction in chromatography [107]. Cellulose acetate fiber has been treated to become a substrate for ion exchange and for immobilization of catalyst [108 110]. 

The tendency of a given component to be attracted to the stationary phase is expressed in chemical terms as an equilibrium constant called the distribution constant, Kc, sometimes also called the partition coefficient. The distribution constant is similar in principle to the partition coefficient that controls a liquid-liquid extraction. In chromatography, the greater the value of the constant, the greater the attraction to the stationary phase. 

In chromatography, the extracting phase that moves through the system. 

Polyethers are usually found in both the filtrate and the mycelial fraction, but in high yielding fermentations they are mosdy in the mycelium because of their low water-solubiUty (162). The high lipophilicity of both the free acid and the salt forms of the polyether antibiotics lends these compounds to efficient organic solvent extraction and chromatography (qv) on adsorbents such as siUca gel and alumina. Many of the production procedures utilize the separation of the mycelium followed by extraction using solvents such as methanol or acetone. A number of the polyethers can be readily crystallized, either as the free acid or as the sodium or potassium salt, after only minimal purification. 

Analytical Supercritical Fluid Extraction and Chromatography Supercritical fluids, especially CO9, are used widely to extrac t a wide variety of solid and hquid matrices to obtain samples for analysis. Benefits compared with conventional Soxhlet extraction include minimization of solvent waste, faster extraction, tunabihty of solvent strength, and simple solvent removal with minimal solvent contamination in the sample. Compared with high-performance liquid chromatography, the number of theoretical stages is higher in... 

Bi-functional radio-analytical scheme, based on exchange and extraction column chromatography, which provides the reliable information on molybdenum and uranium contents in biological materials has been elaborated. The contribution of uranium fission reaction has been strictly monitored. The uncertainty of the results of Mo determination by the presented method is very low. 

Microwave extraction realized at 120 °C for 30 min with Hexane -Acetone (3 2 V/V) as the extraction solvent was identified as the most effective extraction procedure for isolation of TPH from biotic matrices. The aim of this research is to develop a silica gel and alumina fractionation procedure for plant sample extraction. Column chromatography with two solvents (chloroform and hexane dichloromethane) as a mobile phase were used for clean-up of extract. In this research the efficiency of recovery received from chloroform as a mobile phase. 

Epichlorhydrin (ECH) detection starts with detecting epoxide cycle using hydrochloric acid in combination with sodium chloride the reaction product - 1,3-dichlorhydrin - is extracted in diethyl ether and concentrated by removing the latter. Gas-liquid chromatography with a flame-ionization detector is used to detect glycerin 1,3-dichlorhydrin. The sensitivity of the method is 0.01 mg/dm. ... 

Homoallyl alcohol (3) Metalation of (E) butene (1 05 equiv) with n BuLI (t equiv) and KOtBu (1 equiv) in THF at SO C for 15 mm followed by treatment of (E)-crotyl potassum salt with B(OiPr)3 at 79°C gave after quenching with 1 N HCI and extraction with EtjO containing 1 equiv of diisopropyl tartarate. the crotyl boronate 2 A solution of decanall (156 mg 1 mmol) was added to a toluene solution of 2 (1 1 15 equiv) (0 2 M) at 78 C containing 4A molecular sieves (15-20 mg/L) After 3 h at -78°1 N NaOH was added, followed by extraction and chromatography to afford 208 mg of 3 (90%), anti syn 99 1... 

From hen egg white. Purified by solvent extraction and chromatography on alumina. Suspended in distilled water and kept frozen until used [Lee and Hunt J Am Chem Soc 106 7411 1984, Singleton et al. J Am Oil Chem Soc 42 53 7965]. For purification of commercial egg lecithin see Pangborn [J Biol Chem 188 471 7957]. 

Figure 2.12 Schematic representation of an on-line SPE-GC system consisting of three switching valves (VI-V3), two pumps (a solvent-delivery unit (SDU) pump and a syringe pump) and a GC system equipped with a solvent-vapour exit (SVE), an MS instrument detector, a retention gap, a retaining precolumn and an analytical column. Reprinted from Journal of Chromatography, AIIS, A. J. H. Eouter et al, Analysis of microcontaminants in aqueous samples hy fully automated on-line solid-phase extraction-gas chromatography-mass selective detection , pp. 67-83, copyright 1996, with permission from Elsevier Science.

Low-valent titanium was prepared from TiCl4 (9.5 g, 50 mmol) and activated zinc (6.55 g, 100 mmol) in the presence of pyridine (2.5 mL) in THF (400 mL) To this mixture was added all at once the corresponding bipyrroledicarbaldehyde (6 1.36 g, 5 mmol) and the mixture was refluxed for 30 min. After hydrolysis with a 10% aq K.2C03 (125 mL), aqueous extraction and chromatography (silica gel, CH2Cl,/hexane 1 1), the porphycene was obtained as the only nonpolymerized product. Recrystallization (hexane) gave red-violet needles of the porphycene yield 120 mg (10%). 

Chemical forces are normally irreversible in nature (at least in chromatography) and thus, the distribution coefficient of the solute with respect to the stationary phase is infinite or close to infinite. Affinity chromatography is an example of the use of chemical forces in a separation process. The stationary phase is formed in such a manner that it will chemically interact with one unique solute present in the sample and thus, exclusively extract it from the other materials... 

Postigo C, Lopez De Alda MJ, Barcelo D (2008) Fully automated determination in the low nanogram per liter level of different classes of drugs of abuse in sewage water by on-line solid-phase extraction-liquid chromatography-electrospray-tandem mass spectrometry. Anal Chem 80(9) 3123-3134... 

When the aim is isolation for identification by direct probe insertion mass spectrometry (MS), plastic materials, filter papers, and blenders should be avoided to prevent contamination during extraction and chromatography. It is also very important to avoid the cis-trans isomerization of carotenoids in solution, which is accelerated by heat, light, acids, and active surfaces. Therefore, a pure carotenoid or even a crude extract should never be stored in solution it should be kept completely dry in an inert atmosphere at low temperature. 

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