GC methods

Gas chromatographic (GC) methods have been used for determining volatile oxidation products. Static headspace, dynamic headspace or direct injection methods are the three commonly used approaches. These methods were compared in an analysis of volatile compounds in an oxidized soybean oil. It was found that each method produced significantly different GC profiles (Frankel 1985). The dynamic headspace and direct injection methods gave similar results, but the static headspace is more sensitive to low molecular weight compounds. Lee and co-workers (1995) developed a dynamic headspace procedure for isolating and analyzing the volatiles from oxidized soybean oil, and equations were derived from theoretical considerations that allowed the actual concentration of each flavor component to be calculated. 

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The efficiency of separation of solvent from solute varies with their nature and the rate of flow of liquid from the HPLC into the interface. Volatile solvents like hexane can be evaporated quickly and tend not to form large clusters, and therefore rates of flow of about 1 ml/min can be accepted from the HPLC apparatus. For less-volatile solvents like water, evaporation is slower, clusters are less easily broken down, and maximum flow rates are about 0.1-0.5 ml/min. Because separation of solvent from solute depends on relative volatilities and rates of diffusion, the greater the molecular mass difference between them, the better is the efficiency of separation. Generally, HPLC is used for substances that are nonvolatile or are thermally labile, as they would otherwise be analyzed by the practically simpler GC method the nonvolatile substances usually have molecular masses considerably larger than those of commonly used HPLC solvents, so separation is good. 

Direct deterruination of the formamide content by gc methods proves to be inaccurate because of its tendency to decompose at elevated temperatures. This also limits the accuracy of the classical Kjehldahl deterruination. The purity of formamide is, therefore, more reUably deterrnined by analysis of its impurities and substraction of the combined contents from 100%. 

Methanol can be converted to a dye after oxidation to formaldehyde and subsequent reaction with chromatropic acid [148-25-4]. The dye formed can be deterruined photometrically. However, gc methods are more convenient. Ammonium formate [540-69-2] is converted thermally to formic acid and ammonia. The latter is trapped by formaldehyde, which makes it possible to titrate the residual acid by conventional methods. The water content can be determined by standard Kad Eischer titration. In order to determine iron, it has to be reduced to the iron(II) form and converted to its bipyridyl complex. This compound is red and can be determined photometrically. Contamination with iron and impurities with polymeric hydrocyanic acid are mainly responsible for the color number of the merchandized formamide (<20 APHA). Hydrocyanic acid is detected by converting it to a blue dye that is analyzed and deterruined photometrically. 

More specific methods involve chromatographic separation of the retinoids and carotenoids followed by an appropriate detection method. This subject has been reviewed (57). Typically, hplc techniques are used and are coupled with detection by uv. For the retinoids, fluorescent detection is possible and picogram quantities of retinol in plasma have been measured (58—62). These techniques are particularly powerful for the separation of isomers. Owing to the thermal lability of these compounds, gc methods have also been used but to a lesser extent. Recently, the utiUty of cool-on-column injection methods for these materials has been demonstrated (63). 

Chromatographic methods including thin-layer, hplc, and gc methods have been developed. In addition to developments ia the types of columns and eluents for hplc appHcations, a significant amount of work has been done ia the kiads of detectioa methods for the vitamin. These detectioa methods iaclude direct detectioa by uv, fluoresceace after post-column reduction of the quiaone to the hydroquinone, and electrochemical detection. Quantitative gc methods have been developed for the vitamin but have found limited appHcations. However, gc methods coupled with highly sensitive detection methods such as gc/ms do represent a powerful analytical tool (20). 

There are at least three gc methods employed by the ATF, industry, and the government to detect ethyl carbamate. 

What is common to all of these areas is that the relevant number of published GC-GC papers is very small when compared to those concerning single-column and GC-MS methods. While approximately 1000 papers per year are currently published on single-column GC methods and, in recent years, nearly 750 per year on GC-MS techniques, only around 50 per annum have been produced on two-dimensional GC. Of course, this may not be a true reflection of the extent to which two-dimensional GC is utilized, but it is certainly the case that research interest in its application is very much secondary to that of mass spectrometric couplings. A number of the subject areas where two-dimensional methods have been applied do highlight the limitations that exist in single-column and MS-separation analysis. 

This novel manifestation of the gas chromatographic separation demands that Our fundamental understanding of the GC method-invariably of single-dimensional scope-is challenged as follows concepts of column efficiency and separation are now Supplanted by a need to compare the performances of two columns operating... 

On-line coupled LC-GC methods have been developed in food analysis for several reasons, i.e. lower detection limits can be reached, the clean-up is more efficient, and large numbers of samples can be analysed with a minimum of manual sample preparation in shorter times. 

The analysis of sterols, sterols esters, erythrodiol and uvaol, and other minor components of oils and fats, is usually carried out by normal-phase HPLC-HRGC by using a loop-type interface and the concurrent eluent evaporation technique, as reported in the papers cited by Mondello et al. (48) (up to 1995) and in more recent papers (49, 50). More recently, reversed-phase LC-GC methods have been... 

These GC conditions are suitable for analyzing many prostaglandins, thromboxanes, leuko-trienes, and other metabolites of arachidonic acid, such as the hydroxyeicosatetraenoic (HETE) acids. However, the 5-, 12-, and 15-HETE isomers are difficult to separate using GC methods. Sometimes the methyl ester-TMS derivatives provide a better GC separation, or for ketoprostaglandins, the MO-methyl ester-TMS derivatives often give a better separation... 

As sulfonic acid cannot be vaporized, its determination by the direct gas chromatography (GC) method is not possible. To enable determination by GC, the reactivity of the S03H group is used the esterification of the S03H group with diazomethane via acid chloride is one way to transfer the sulfonic acid to volatile compounds. By conversion of the sulfonic acid with phosphoric acid at 200-210°C, the S03H group is cleaved and the hydrocarbons are obtained [184-186]. 

One of the most frequent techniques for analyzing 1,4-dioxane is gas chromatography. Birkel et al. [319] proposed in 1979 a gas chromatographic method based on partial vacuum distillation of the sample, analyzing polysorbate 60 and 80 with sensitivity to the 0.5 ppm. Stafford et al. [320] proposed a direct injection GC method which meant an improvement to the Birkel s technique. Robinson and Ciurczak [321] described a direct GC method for the analysis of... 

For single-carbon-number AOS samples, analyses can be performed satisfactorily using just the GC method. For multicarbon-number AOS samples that have high sultone content (about 50 ppm), the LC method provides adequate resolution and sensitivity. However, for multicarbon-number AOS samples containing normal sultone levels and for AES samples, the combined LC-GC method is necessary to obtain the required separation and detection levels. Additionally, the combined method is advantageous in eliminating interferences in the LC method that are sometimes observed with AOS samples that have been bleached. 

The relative standard deviation RSD (or c.o.v. = coefficient of variation ) is constant over the whole range, such as in many GC methods, that is, the standard deviation Sy is proportional to y. 

Pilz-Giither, D. and Speer, K. (2004). Development of a GC method for the simultaneous determination of organic acids in honey. Dtsch. Lebensm. Rundsch. 100,84-87. 

The following physico-chemical properties of the analyte(s) are important in method development considerations vapor pressure, ultraviolet (UV) absorption spectrum, solubility in water and in solvents, dissociation constant(s), n-octanol/water partition coefficient, stability vs hydrolysis and possible thermal, photo- or chemical degradation. These valuable data enable the analytical chemist to develop the most promising analytical approach, drawing from the literature and from his or her experience with related analytical problems, as exemplified below. Gas chromatography (GC) methods, for example, require a measurable vapor pressure and a certain thermal stability as the analytes move as vaporized molecules within the mobile phase. On the other hand, compounds that have a high vapor pressure will require careful extract concentration by evaporation of volatile solvents. 

On the other hand, if only specific GC detectors, e.g. the electron capture, nitrogen-phosphorus or flame photometric detectors, are tested, the argument of lack of GC method sensitivity is not acceptable. In most cases mass spectrometric detectors provide the sensitivity and selectivity needed. Unfortunately, tandem mass spectrometry (MS/MS) or MS" detectors for GC are still not widely used in official laboratories, and therefore these techniques are not always accepted for enforcement methods. 

In 1994, only 15% of EPA method validations (tolerance method validation and environmental chemistry method validations) that involved GC were carried out using GC/MS. In 2002, this number is reversed in that 85% of the GC methods that were validated by both programs used GC/MS. Many of the compounds investigated in these method trials were polar compounds, and hence these compounds required derivatization in order to be amenable to GC. One common methylating agent is (trimethylsilyl)diazomethane, which is used, for example, to methylate the sulfonamide flumetsulam. As opposed to HPLC/MS, where derivatization is often not necessary, the GC/MS procedure involves an extra step to methylate this compound, under dry conditions, prior to determination by GC/MS. 

For the GC method, the generated carbon disulfide is analysed using a flame photomeric detector in the sulfur mode. The acid decomposition is carried out in a sealed glass container at 80 °C, and an aliquot of the headspace is injected into a gas chromatograph. " ... 

Acetamiprid and its metabolites. A GC method has been developed for the determination of acetamiprid and its metabolites IM-2-1, IM-0, IC-0 (Figure 4) and IM-O-glucose in crops. As shown in Figure 5, acetamiprid and its metabolites in crops are extracted with methanol and derivatized to methyl 6-chloronicotinate (IC-O-Me) through alkaline hydrolysis, potassium permanganate oxidation and then esterification... 

In the GC method, the recoveries of acetamiprid and its degradation products in soil are >95% by the individual method for the parent compound (parent determination method). On the other hand, the recovery ranged from 74 to 96% by the total residue determination method with a limit of detection of 0.01 mg kg ... 

The official enforcement method is a GC method, but the method described here is quicker and more robust. Approximately 36 samples can be analyzed within 24 h. 

For the development of the LANA route, analytical techniques such as GC, TLC, FIPLC, NMR, and GC/MS were used. GC methods were developed to monitor formation of the Grignard reagent. Since all of the components of the LANA route are unstable to the elevated temperatures of GC, FIPLC and TLC techniques were chosen for qualitative and quantitative analysis of reaction samples, to monitor reaction progress, and to determine the purity of intermediates and final product. Because the process development time was limited and the LANA process was entirely dependent on HPLC analysis, we set criteria for the development of HPLC methods ... 

Table 3.45 lists the main characteristics of SPME. The technique is sensitive, reduces analyte loss and can successfully be applied to the analysis of both polar and nonpolar volatile and nonvolatile analytes from solid or liquid and in the gas phase [535]. Room temperature operation of SPME favours thermolabile compounds (only heating during injection into GC). Method... 

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