Chromatographic methods application

Zitko [20] has described a confirmatory method in which the chloroparaffins in sediments are reduced to normal hydrocarbons which are then analysed by gas chromatography. This method lacks sufficient sensitivity for trace (sub-ppm) analysis and the confirmatory method may be difficult to apply. Friedman and Lombardo [21] have described a gas chromatographic method applicable to chloroparaffins that are slightly volatile the method is based on microcoulometric detection and photochemical elimination of chlorinated aromatic compounds that otherwise interfere. 

PLA Planas, J., Lefebvre, D., Tjemeld, F., and Hahn-Haegerdal, B., Analysis of phase compo-sition in aqueous two-phase systems using a two-column chromatographic method Application to lactic acid production by extractive fermentation, Biotechnol. Bioeng., 54, 303, 1997. 

Joseph M H (1978) Determination of kynurenme by a simple gas-liquid chromatographic method applicable to urine, plasma, brain, and cerebrospinal fluid. J. Chromatogr. 146, 33-41. 

Simple Gas-Liquid Chromatographic Method Applicable to Urine, Plasma, Brain and Cerebrospinal Fluid J. Chromatogr. 146(1) 33-41 (1978) ... 

Tsvet M (1906) Adsorption analysis and chromatographic method. Application to the chemistry of chlorophyll. Ber Dtsch Bot Ges 24 384-393... 

In practice of chemical analysis of organic substances, for some classes of compounds measuring of summary concentration in re-count to one of representatives is used. In the case of need of information about the content of each component, the chromatographic methods are applicable. 

For selective estimation of phenols pollution of environment such chromatographic methods as gas chromatography with flame-ionization detector (ISO method 8165) and high performance liquid chromatography with UV-detector (EPA method 625) is recommended. For determination of phenol, cresols, chlorophenols in environmental samples application of HPLC with amperometric detector is perspective. Phenols and chlorophenols can be easy oxidized and determined with high sensitivity on carbon-glass electrode. 

In the post-World War II years, synthesis attained a different level of sophistication partly as a result of the confluence of five stimuli (1) the formulation of detailed electronic mechanisms for the fundamental organic reactions, (2) the introduction of conformational analysis of organic structures and transition states based on stereochemical principles, (3) the development of spectroscopic and other physical methods for structural analysis, (4) the use of chromatographic methods of analysis and separation, and (5) the discovery and application of new selective chemical reagents. As a result, the period 1945 to 1960 encompassed the synthesis of such complex molecules as vitamin A (O. Isler, 1949), cortisone (R. Woodward, R. Robinson, 1951), strychnine (R. Woodward, 1954), cedrol (G. Stork, 1955), morphine (M. Gates, 1956), reserpine (R. Woodward, 1956), penicillin V (J. Sheehan, 1957), colchicine (A. Eschenmoser, 1959), and chlorophyll (R. Woodward, 1960) (page 5). ... 

Multidimensional chromatography has important applications in environmental analysis. Environmental samples may be very complex, and the fact that the range of polarity of the components is very wide, and that there are a good many isomers or congeners with similar or identical retention characteristics, does not allow their separation by using just one chromatographic method. 

In order to reduce or eliminate off-line sample preparation, multidimensional chromatographic techniques have been employed in these difficult analyses. LC-GC has been employed in numerous applications that involve the analysis of poisonous compounds or metabolites from biological matrices such as fats and tissues, while GC-GC has been employed for complex samples, such as arson propellants and for samples in which special selectivity, such as chiral recognition, is required. Other techniques include on-line sample preparation methods, such as supercritical fluid extraction (SFE)-GC and LC-GC-GC. In many of these applications, the chromatographic method is coupled to mass spectrometry or another spectrometiic detector for final confirmation of the analyte identity, as required by many courts of law. 

Gravimetric, photometric, chromatographic, enzymatic, and microbiological methods for the determination of amino acids are reviewed and discussed. Marked advances have been made during the present decade in methods applicable to the determination of amino acids, and with the development of new analytical methods it should soon be possible to determine all the amino acids of biological importance with a degree of accuracy sufficient for practical as well as many theoretical purposes. 

The columns labeled PI reflect the total of pyrethrin I and cinerin I just as in the AO AC procedure. The gas chromatographic results are in terms of the total amount of the mixture but were analyzed as the methyl ester of chrysanthemic acid. The present state of the determination of PII (pyrethrin II plus cinerin II) is not complete because of the erratic extractability of the dicarboxylic acids from the hydrolysis mixture. The gas chromatographic pattern is distinct and straightforward. As the extraction procedure for PII is improved, the gas chromatographic method will be more applicable. The present recovery of PII is in the range of 80 to 90%. The average of the values shown in Table II for PI is 98.0%. 

K. Mehlhose, Explosivstoffe 20 (3-4), 37-70 (1972) CA 78, 113513 (1973) Methods developed for detn of H20 in gun and rocket propints are column distn with n-PrOH and gas-chromatographic analysis of the distillate, corrected for continuous formation of water in decompn reactions and photometric methods, both based on the reaction of CoCl2 with water. Choice of the methods is based on a critical review (117 refs) of the usual methods of water detn by chemical and physical methods. A theoretical and exptl analysis of the new methods was made and their results compared with those of older methods. Application to mono-, di-, and tribasic and to double-base NC and poly (vinyl nitrate) propints is discussed... 

It follows that measurements must be made with a precision of about 0.2 second if quantitative results are to be of any value. It is seen from figure 4 that the experimental points lie very close to the line and a fairly accurate measurement of the distribution of the two isotopes can be obtained from retention time measurements. This method has very limited areas of application and is given here, more to demonstrate the effect of unresolved impurities on retention time, than to suggest it as an alternative to adequate chromatographic resolution. In some cases, however, particularly in the analysis of isotopes, it may be the only practical way to obtain a quantitative evaluation of the mixture by a liquid chromatographic method. 

The purpose of this final chapter is to provide the analyst with a background of practical examples to aid in the selection of, firstly, the best chromatographic method and, secondly, the best phase system when faced with an hitherto unknown sample for analysis. The literature is rich with LC applications and frequently publications are available for the separation of closely similar mixtures to that of the sample. It is unlikely, however, that the chromatographic conditions for the actual separation required will be available and, even if they are, the conditions reported may well not be optimum. This is more likely to be true for those applications that are described in earlier publications. Nevertheless, conditions that have be successfully employed for related separations may certainly help to identify those conditions necessary for the sample supplied for assay. 

The possibility of using the hexakisamino-compound, N3P3(NH2)e (obtained by ammonolysis of NgPaCle), as a fertilizer for barley has been demonstrated.In most respects it is superior to the ammonium phosphates, although not as far as costs are concerned. There are obvious links between this application and the course of hydrolysis of NgPafNHale, which has recently been followed by paper chromatographic methods. 

MAiANi G, SERAFiNi M, SALUCCi M, AZZiNi E and FERRO-Luzzi A (1997) Application of a new high-performance liquid chromatographic method for measuring selected polyphenols in hiunan plasma , J of Chromatog B, 692, 311-17. 

After the extrachon of total lipids from four different genotypes of flax seed (Linum usitassimum) differing markedly in their acyl composihon, PTLC was used for the isolahon of different lipid classes in the neutral lipid frachon [69]. Application of planar chromatographic methods, including PTLC, in the separahon of food lipids has been reviewed with 40 references by Olsson [70]. The polar lipid fraction of niger seed (Guizotia abyssinica Cass.) collected from different regions of Ethiopia could be separated by PTLC on silica gel [71]. 

Gas and liquid chromatography directly coupled with atomic spectrometry have been reviewed [178,179], as well as the determination of trace elements by chromatographic methods employing atomic plasma emission spectrometric detection [180]. Sutton et al. [181] have reviewed the use and applications of ICP-MS as a chromatographic and capillary electrophoretic detector, whereas Niessen [182] has briefly reviewed the applications of mass spectrometry to hyphenated techniques. 

Table 7.40 summarises the general characteristics of on-line SFC-MS. The method is potentially most useful for thermally labile and involatile compounds that are unsuitable for GC-MS. Because the MS instrument is the main source of information, the reproducibility of the retention and the separation selectivity are much less important than for other SFC applications. As a result, mass spectroscopists do not feel restrained by the limits on reproducibility, which slowed the uptake of SFC by chromatographers. Method development should not be underestimated. Practical problems are associated with interfacing and the effect of the expanding... 

In polymer/additive analysis, spectroscopic methods are used for studying both molecular and atomic composition, usually as a detector for chromatographic techniques. Application of spectroscopic techniques to molecular additive analysis depends on the nature of the sample and its complexity (Table 10.26). Application of the intrinsically simple monocomponent analyses by means of UV/VIS and FUR is rather exceptional for real-life samples. Most industrial samples are complex. It is in the area of multicomponent analysis that most... 

Aleksic et al. [47] estimated the hydrophobicity of miconazole and other antimycotic drugs by a planar chromatographic method. The retention behavior of the drugs have been determined by TLC by using the binary mobile phases acetone-n-hexane, methanol toluene, and methyl ethyl ketone toluene containing different amounts of organic modifier. Hydrophobicity was established from the linear relationships between the solute RM values and the concentration of organic modifier. Calculated values of RMO and CO were considered for application in quantitative structure activity relationship studies of the antimycotics. 

One of the earliest applications of gas chromatography to marine problems was in the measurement of fatty acids in seawater. In general, the gas chromatographic method has employed extraction into organic solvent, followed by the... 

---