Alkanes analysis

Mineral Oil Hydraulic Fluids. Methods are available for analysis of the hydrocarbon components of mineral oil hydraulic fluids (predominantly straight and branched chain alkanes) in environmental samples. Some of these methods are summarized in Table 6-3. In general, water and sediment samples are extracted with a suitable solvent in a Soxhlet extractor (for solid samples) or in separatory funnel or shake flask (for liquid samples) (Bates et al. 1984 Peterman et al. 1980). The extract is cleaned up on silica gel or Florisil columns using a nonpolar solvent to elute the nonpolar alkanes. Analysis is usually performed by GC/MS (Bates et al. 1984 Kawamura and Kaplan 1983 Peterman et al. 1980). Method performance has not been reported, although 82% recovery of aliphatic hydrocarbons was reported for rainwater (Kawamura and Kaplan 1983). 

Olive oil is often illegally adulterated with other less expensive vegetable oils. Oils widely used for this purpose include olive pomace oil, corn oil, peanut oil, cottonseed oil, sunflower oil, soybean oil, and poppy seed oil. °° Among the varions chemical and physical methods employed toward the detection of the adulteration of olive oil by low-grade olive oils and seed oils are (a) Sterol analysis (presence of stigmasterol and 3-sitosterol), (b) alkane analysis (C27, C29, and C31), (c) wax and aliphatic alcohol analysis, (d) fatty acids/(with HPLC) trans fatty acid, and (e) Triacylglycerol. 

Bird, M. L, R. E. Summons, M. K. Gagan, Z. Roksandic, L. Dowling, J. Head, L. K. Fifield, R. G. Cresswell D. P. Johnson, 1995. Terrestrial vegetation change inferred from n-alkane analysis in the marine environment. Geochim. Cosmochim. Acta 59 2853-2857. 

In this chapter we 11 examine the conformations of various alkanes and cyclo alkanes focusing most of our attention on three of them ethane butane and cyclo hexane A detailed study of even these three will take us a long way toward understanding the mam ideas of conformational analysis... 

Surface SHG [4.307] produces frequency-doubled radiation from a single pulsed laser beam. Intensity, polarization dependence, and rotational anisotropy of the SHG provide information about the surface concentration and orientation of adsorbed molecules and on the symmetry of surface structures. SHG has been successfully used for analysis of adsorption kinetics and ordering effects at surfaces and interfaces, reconstruction of solid surfaces and other surface phase transitions, and potential-induced phenomena at electrode surfaces. For example, orientation measurements were used to probe the intermolecular structure at air-methanol, air-water, and alkane-water interfaces and within mono- and multilayer molecular films. Time-resolved investigations have revealed the orientational dynamics at liquid-liquid, liquid-solid, liquid-air, and air-solid interfaces [4.307]. 

The main product, benzene, is represented by solute (B), and the high boiling aromatics are represented by solute (C) (toluene and xylenes). The analysis of the products they obtained are shown in Figure 12. The material stripped form the top section (section (1)) is seen to contain the alkanes, alkenes and naphthenes and very little benzene. The product stripped from the center section appears to be virtually pure benzene. The product from section (3) contained toluene, the xylenes and thiophen which elutes close to benzene. The thiophen, however, was only eliminated at the expense of some loss of benzene to the lower stripping section. Although the system works well it proved experimentally difficult to set up and maintain under constant operating conditions. The problems arose largely from the need to adjust the pressures that must prevent cross-flow. The system as described would be virtually impossible to operate with a liquid mobile phase. 

A method has been developed which determines the amount of residual alk-ene and secondary alcohol in AOS using an aqueous-organic extraction solvent system followed by GC analysis. Alkanes present (impurities in the feedstock) will also be determined with the unreacted alkene. 

In a combustion analysis, 3.21 g of a hydrocarbon formed 4.48 g of water and 9.72 g of carbon dioxide. Deduce its empirical formula and state whether it is likely to be an alkane, an alkene, or an alkyne. Explain your reasoning. 

The relative probabilities of Reactions 24, 25, and 26 were, respectively, 1.00, 0.25, and 0.12 at a hydrogen pressure of about 1 atmosphere (9). These numbers could be derived either by analyzing the stable alkanes formed in the unimolecular decompositions (Reactions 24-26) or from the products of the hydride transfer reactions between C5Hi2 and the alkyl ions. Elimination of H2 from protonated pentane may also occur, but it is difficult (although not impossible) to establish this reaction through neutral product analysis. 

In the same spirit DFT studies on peroxo-complexes in titanosilicalite-1 catalyst were performed [3]. This topic was selected since Ti-containing porous silicates exhibited excellent catalytic activities in the oxidation of various organic compounds in the presence of hydrogen peroxide under mild conditions. Catalytic reactions include epoxidation of alkenes, oxidation of alkanes, alcohols, amines, hydroxylation of aromatics, and ammoximation of ketones. The studies comprised detailed analysis of the activated adsorption of hydrogen peroxide with... 

Smits THM, SB Balada, B Witholt, JB van Beilen (2002) Eunctional analysis of alkane hydroxylases from Gram-negative and Gram-positive bacteria. J Bacterial 184 1733-1742. 

The reaction can be easily monitored by IR spectroscopy since surface silanols give a characteristic peak at 3747 cm hi order to establish the mass balance, it is necessary to obtain an elemental analysis of the solid (M, C, H, N. ..) and to measure the amoimt of alkane evolved Wing grafting. 

---