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Standard methods, liquid chromatography

ASTM Standard E 755-90, "Standard Test Method for Assay of Dicumyl Peroxide by Liquid Chromatography," in Ref. 253. [Pg.139]

A number of analytical methods have been developed for the determination of chlorotoluene mixtures by gas chromatography. These are used for determinations in environments such as air near industry (62) and soil (63). Liquid crystal stationary columns are more effective in separating m- and chlorotoluene than conventional columns (64). Prepacked columns are commercially available. ZeoHtes have been examined extensively as a means to separate chlorotoluene mixtures (see Molecularsieves). For example, a Y-type 2eohte containing sodium and copper has been used to separate y -chlorotoluene from its isomers by selective absorption (65). The presence of ben2ylic impurities in chlorotoluenes is determined by standard methods for hydroly2able chlorine. Proton (66) and carbon-13 chemical shifts, characteristic in absorption bands, and principal mass spectral peaks are available along with sources of reference spectra (67). [Pg.54]

The malonaldehyde thus formed can be estimated quantitatively by the thiobarbituric acid method (58, 59). As a control of the method s reliability, we used, as primary standard, 1, 3, 3-tri-ethoxypropene (46, 47) purified by gas-liquid chromatography (56) and hydrolyzed to malonaldehyde at room temperature with IN sulfuric acid. The molar... [Pg.114]

High performance liquid chromatography is used for the separation and quantitative analysis of a wide variety of mixtures, especially those in which the components are insufficiently volatile and/or thermally stable to be separated by gas chromatography. This is illustrated by the following method which may be used for the quantitative determination of aspirin and caffeine in the common analgesic tablets, using phenacetin as internal standard where APC tablets are available the phenacetin can also be determined by this procedure. [Pg.233]

Figure 5.67 Reconstructed ion chromatograms for Idoxifene and internal standard (ds-Idoxifene using LC-ToF-MS for (a) double-blank human plasma extract, (b) extract of blank human plasma containing internal standard (IS), and (c) control-blank human plasma spiked with Idoxifene at 5 gml , the LOQ of the method. Reprinted from 7. Chromatogr., B, 757, Comparison between liquid chromatography-time-of-flight mass spectrometry and selected-reaction monitoring liquid chromatography-mass spectrometry for quantitative determination of Idoxifene in human plasma , Zhang, H. and Henion, J., 151-159, Copyright (2001), with permission from Elsevier Science. Figure 5.67 Reconstructed ion chromatograms for Idoxifene and internal standard (ds-Idoxifene using LC-ToF-MS for (a) double-blank human plasma extract, (b) extract of blank human plasma containing internal standard (IS), and (c) control-blank human plasma spiked with Idoxifene at 5 gml , the LOQ of the method. Reprinted from 7. Chromatogr., B, 757, Comparison between liquid chromatography-time-of-flight mass spectrometry and selected-reaction monitoring liquid chromatography-mass spectrometry for quantitative determination of Idoxifene in human plasma , Zhang, H. and Henion, J., 151-159, Copyright (2001), with permission from Elsevier Science.
In a study of the metabolism of methyl parathion in intact and subcellular fractions of isolated rat hepatocytes, a high performance liquid chromatography (HPLC) method has been developed that separates and quantitates methyl parathion and six of its hepatic biotransformation products (Anderson et al. 1992). The six biotransformation products identified are methyl paraoxon, desmethyl parathion, desmethyl paraoxon, 4-nitrophenol, />nitrophenyl glucuronide, and /wiitrophenyl sulfate. This method is not an EPA or other standardized method, and thus it has not been included in Table 7-1. [Pg.178]

Shatkay, A., Effect of Concentration on the Internal Standards Method in Gas-Liquid Chromatography, Ana/. Chem. 50, 1978, 1423-1429. [Pg.408]

Successful use of modern liquid chromatography in the clinical laboratory requires an appreciation of the method s analytical characteristics. The quantitative reproducibility with respect to peak height or peak area is quite good. With a sample loop injector relative standard deviations better than 1% are to be expected. The variability of syringe injection (3-4% relative standard deviation) requires the use of an internal standard to reach the 1% level (2,27). [Pg.236]

The enforcement methods provided by the applicants give basic information about appropriate cleanup steps and specific determination procedures. Typically, direct use of this developmental work occurred when a GC multi-residue method was found appropriate. Owing to the recent developments in the field of MS/MS with atmospheric pressure ionization, an alternative approach for those compounds that can be analyzed by liquid chromatography (LC) will soon be possible. It is important that some fundamental considerations for such method(s) should be agreed at the outset. Considerations include the most suitable extraction solvents and cleanup steps and some standard HPLC conditions. [Pg.111]

The method for chloroacetanilide soil metabolites in water determines concentrations of ethanesulfonic acid (ESA) and oxanilic acid (OXA) metabolites of alachlor, acetochlor, and metolachlor in surface water and groundwater samples by direct aqueous injection LC/MS/MS. After injection, compounds are separated by reversed-phase HPLC and introduced into the mass spectrometer with a TurboIonSpray atmospheric pressure ionization (API) interface. Using direct aqueous injection without prior SPE and/or concentration minimizes losses and greatly simplifies the analytical procedure. Standard addition experiments can be used to check for matrix effects. With multiple-reaction monitoring in the negative electrospray ionization mode, LC/MS/MS provides superior specificity and sensitivity compared with conventional liquid chromatography/mass spectrometry (LC/MS) or liquid chromatography/ultraviolet detection (LC/UV), and the need for a confirmatory method is eliminated. In summary,... [Pg.349]

Bogusz, M., Franke, J. P., de Zeeuw, R. A., and Erkens, M., An overview of the standardization of chromatographic methods for screening analysis in toxicology by means of retention indices and secondary standards. Part II. High performance liquid chromatography, Fresenius ]. Anal. Chem., 347, 73, 1993. [Pg.195]

Analysts in industry prefer in many cases to maintain consistent methods for their analyses. Recommended ASTM analytical procedures are quite well developed in the rubber and polymer industry. As an example, we mention the standard test method for determination of phenolic antioxidants and erucamide slip additives in LDPE using liquid chromatography [76]. However, the current industry standard test methods (ASTM, AOAC, IUPAC, etc.) use a large number of solvents in vast... [Pg.17]

ASTM D 1996-97, Standard Test Method for Determination of Phenolic Antioxidants and Erucamide Slip Additives in Low Density Polyethylene Using Liquid Chromatography (LC), Annual Book of ASTM Standards, ASTM, West Conshohocken, PA (1997), Vol. 08.01. [Pg.27]


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See also in sourсe #XX -- [ Pg.299 ]




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