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Methylated , gas-liquid

Fenopropimorph and metabolite fenopropimorphic acid fungicide Acetone - water, partitioning with methylene chloride Gel permeation chromatography Methylation - gas liquid chromatography with NP detection and GC-MS [78]... [Pg.7]

The separation of mixtures involving N-methyl-JLtetrahydropyridines into their pure components by means of gas-liquid chromatography was discussed in a report by Holik et al. (87). They found that, using tris(/3-cyanoethoxymethyl)-y-picoline as the stationary phase, the primary factors involved in the specific retention volumes of these enamines is the electronic effect of a methyl substituent and the nitrogen atom on the carbon-carbon double bond. It was observed that 1,3-dimethyl-Zl -tetrahydropyridine (141) has a smaller specific retention volume and, hence, is eluted before... [Pg.50]

Like propane, n-hutane is mainly obtained from natural gas liquids. It is also a hy-product from different refinery operations. Currently, the major use of n-hutane is to control the vapor pressure of product gasoline. Due to new regulations restricting the vapor pressure of gasolines, this use is expected to he substantially reduced. Surplus n-butane could be isomerized to isobutane, which is currently in high demand for producing isobutene. Isobutene is a precursor for methyl and ethyl tertiary butyl ethers, which are important octane number boosters. Another alternative outlet for surplus n-butane is its oxidation to maleic anhydride. Almost all new maleic anhydride processes are based on butane oxidation. [Pg.174]

Jaglan PS, Gunther FA. 1970. Single column gas liquid chromatography of methyl parathion and metabolites using temperature programming. Bull Environ Contam Toxicol 5 111-114. [Pg.214]

Jaglan PS, March RB, Fukuto TR, et al. 1970. Gas-liquid chromatographic determination of methyl parathion and metabolites. J Agric Food Chem 18 809-813. [Pg.214]

Table 5.2 Comparison of reaction conditions and results for hydrogenation of methyl (Z)-a-acetamidocinnamate in mini batch, micro liquid/liquid and micro gas/liquid reactors [70. ... Table 5.2 Comparison of reaction conditions and results for hydrogenation of methyl (Z)-a-acetamidocinnamate in mini batch, micro liquid/liquid and micro gas/liquid reactors [70. ...
The extracted fractions were esterified with either BF3-MeOH reagent or diazomethane and analyzed by GLC. Gas liquid chromatography (GLC) was conducted with a Perkin-Elmer Sigma 3 equipped with flame ionization detector. Separations were obtained on a Hewlett Packard 12 m x 0.2 mm i.d. capillary column coated with methyl silicon fluid (OV-101). The temperature was maintained at 80°C for 2 min then programmed from 80 to 220°C at 8°C/min. The injector temperature was 250°C. Mass spectra were obtained on a Hewlett Packard model 5995 GC-MS mass spectrometer, equipped with a 15 m fused silica capillary column coated with 5% phenyl methyl silicone fluid. Spectra were obtained for major peaks in the sample and compared with a library of spectra of authentic compounds. [Pg.103]

Analysis Techniques. The contents of the major breakdown products of xetralin (naphthalene and 1-methyl indan) present in the distillate were determined by gas-liquid chromatography using a Hewlett Packard Series 5750 Research Chromatograph with a 62m x 0.5mm diameter glass capillary SCOT column coated with nonpolar SE 30 liquid phase (see Reference (4 ) for details). [Pg.245]

Haworth methylation of methyl /3-D-glucopyranoside and its 4-benzyl and 4-(tetrahydropyran-2-yl) ethers was investigated in connection with partial-methylation studies on cellulose.267 For the unsubstituted glycoside, the ratios of relative rate-constants k2 k3 k4 k were estimated to be 8 2 1 8, and, for the 4-ethers, it was found that ke> k2> k3 best agreements between calculated and experimental yields were found with the assumption that the rate constant for reaction at HO-3 is doubled when HO-2 is substituted. Later methylation studies,268 performed to low degrees of substitution, with analysis by gas-liquid chromatography, gave k2> k4> k3 for the reactivity... [Pg.56]

A typical elution profile the separation of saturated esters by gas-liquid chromatography 1. methyl formate 2. methyl acetate 3. ethyl formate 4. ethyl acetate 5. -propyl formate 6. iso-propyl acetate 7. w-butyl formate 8. sec-butyl acetate 9. iso-butyl acetate 10. n-butyl acetate... [Pg.92]

Szeto SY, Brown MJ. 1982. Gas-liquid chromatographic methods for determination of disulfoton, phorate, oxydemeton-methyl and their toxic metabolites in asparagus tissue and soil. J Agric Food Chem 30 1082-1086. [Pg.197]

Many industrial processes involve mass transfer processes between a gas/vapour and a liquid. Usually, these transfer processes are described on the basis of Pick s law, but the Maxwell-Stefan theory finds increasing application. Especially for reactive distillation it can be anticipated that the Maxwell-Stefan theory should be used for describing the mass transfer processes. Moreover, with reactive distillation there is a need to take heat transfer and chemical reaction into account. The model developed in this study will be formulated on a generalized basis and as a consequence it can be used for many other gas-liquid and vapour-liquid transfer processes. However, reactive distillation has recently received considerable attention in literature. With reactive distillation reaction and separation are carried out simultaneously in one apparatus, usually a distillation column. This kind of processing can be advantageous for equilibrium reactions. By removing one of the products from the reactive zone by evaporation, the equilibrium is shifted to the product side and consequently higher conversions can be obtained. Commercial applications of reactive distillation are the production of methyl-... [Pg.1]


See other pages where Methylated , gas-liquid is mentioned: [Pg.64]    [Pg.65]    [Pg.64]    [Pg.65]    [Pg.656]    [Pg.1029]    [Pg.1030]    [Pg.102]    [Pg.550]    [Pg.571]    [Pg.108]    [Pg.39]    [Pg.127]    [Pg.391]    [Pg.214]    [Pg.313]    [Pg.4]    [Pg.261]    [Pg.269]    [Pg.785]    [Pg.327]    [Pg.78]   


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