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Hydrocarbons special

Not to be Used Water, foam, carbon dioxide, or halogenated hydrocarbons Special Hazards of Combustion Products No data Behavior in Fire Reacts violently with water, forming flammable and explosive hydrogen gas. This product may spontaneously ignite in air Ignition Temperature No data Electrical Hazard Not pertinent Burning Rate Not pertinent. [Pg.323]

In case of hydrophobic compounds, which strongly adsorb to particles, e.g. pentabro-modiphenylether or 5 and 6 ring polycyclic aromatic hydrocarbons, special care is required to ensure complete extraction of the particle bound fraction. Separate analysis of SPM and of the liquid would be a good option. If it can be justified, for example, by consideration of contaminant partitioning, analysis of the SPM fraction as surrogate for whole water might be appropriate. Nevertheless, in water bodies with extremely low SPM content (<3mg/L) the dissolved fraction of those contaminants contributes significantly to the total concentration, and hence, has to be taken into account. [Pg.26]

Espitalie, J., Lafargue, E. Eggen, S. 1991. Petroleum potential of terrestrial and marine organic matter in Jurassic sequences of the northern North Sea and Offshore mid-Norway. In Spencer, A. M. (ed.) Generation, Accumulation and Production of Europe s Hydrocarbons. Special Publication of the European Association of Petroleum Geoscientists, 1, Oxford University Press, 49-63. [Pg.367]

Lithium differs from the other alkali metals in that it directs the polymerization of butadiene or isoprene predominantly to 1,4 addition structures. In the case of lithium-catalyzed polyiso-prene, the 1,4 addition structures are all cis. The other alkali metals direct the polymerization of butadiene largely to the 1,2 addition structure and isoprene largely to the 3,4 addition structure. The differences in physical properties, accompanying the structural variations mentioned above, are illustrated by the example of lithium-catalyzed polybutadiene. Lithium, sodium, and potassium are used most conveniently as polymerization catalysts by converting them to metal dispersions in petroleum jelly or other inert hydrocarbons. Special care must be used in handling rubidium or cesium metal. [Pg.26]

The donor-acceptor acyl chloride-aluminium chloride complex is not only an electrophilic reagent but also a hydride ion acceptor (oxidizing reagent). The best hydride donors are the saturated hydrocarbons, specially those containing a tertiary carbon atom. The acylation of cyclohexane is an old and well-known reaction giving acetyl-methyl-cyclopentene and/or -cyclopentane. 26,27 the yields are low because the solvent used was either cyclohexane itself or small quantities of chloroform. in our hands, we found that the reaction carried out in methylene chloride solution ( IM) led to the l-acetyl-2-methylcyclopentene and l,3-diacetyl-2-methylcyclopentene Z in good yields. A cleaner reaction also occurred from methylcyclopentane. The ratio of ys could be changed by modification of the reaction conditions (see Table 1) (overall yields of the hydrocarbons functionalization were around 75-80 %). [Pg.130]

Ledbury, W. and Biair,E. W., TbeProdiiction of Formaldehyde by Oxidation of Hydrocarbon , Special Report No. 1, pp. 31-4, London, Dept, of Scientific and Industrial Research, Published under the Authority of Hifi Majesty s Stationerj Office, 1937. [Pg.47]

The main synthetic fluids used as special lubricants are esters, polyglycols, silicones, halogenated hydrocarbons and polyphenyl ethers. [Pg.243]

This type of analysis requires several chromatographic columns and detectors. Hydrocarbons are measured with the aid of a flame ionization detector FID, while the other gases are analyzed using a katharometer. A large number of combinations of columns is possible considering the commutations between columns and, potentially, backflushing of the carrier gas. As an example, the hydrocarbons can be separated by a column packed with silicone or alumina while O2, N2 and CO will require a molecular sieve column. H2S is a special case because this gas is fixed irreversibly on a number of chromatographic supports. Its separation can be achieved on certain kinds of supports such as Porapak which are styrene-divinylbenzene copolymers. This type of phase is also used to analyze CO2 and water. [Pg.71]

Identification of normal paraffins by chromatography presents no special problems with the exception of biodegraded crudes, they are clearly distinguished. The problem encountered is to quantify, as shown in Figure 3.14, the normal paraffin peaks that are superimposed on a background representing other hydrocarbons. [Pg.73]

MM2 was, according the web site of the authors, released as MM2 87). The various MM2 flavors are superseded by MM3, with significant improvements in the functional form [10]. It was also extended to handle amides, polypeptides, and proteins [11]. The last release of this series was MM3(%). Further improvements followed by starting the MM4 series, which focuses on hydrocarbons [12], on the description of hyperconjugative effects on carbon-carbon bond lengths [13], and on conjugated hydrocarbons [14] with special emphasis on vibrational frequencies [15]. For applications of MM2 and MM3 in inorganic systems, readers are referred to the literature [16-19]. [Pg.350]

Since aliphatic hydrocarbons (unlike aromatic hydrocarbons, p. 155) can be directly nitrated only under very special conditions, indirect methods are usually employed for the preparation of compounds such as nitroethane, CjHsNO. When ethyl iodide is heated with silver nitrite, two isomeric compounds are formed, and can be easily separated by fractional distillation. The first is the true ester, ethyl nitrite, C,HiONO, of b.p. 17° its identity is shown by the action of hot sodium hydroxide solution, which hydrolyses it, giving ethanol and... [Pg.131]

File 4-.5. An Approximate Input File for the Water Molecule. A hydrogen attached to an oxygen has the special atom designator 21 as distinct from the designator. n in hydrocarbons. [Pg.110]

Firestone at al. " demonstrated the importance of solvent density in the special case of intramolecular Diels-Alder reaction in highly viscous media. Efficient packing of the hydrocarbon solvent was... [Pg.9]

Chapters III to VII discuss the general properties of thiazoles having hydrocarbon and functional substituents, respectively. A special chapter (Chapter VIII) is devoted to mcso-ionic thiazoles, and Chapter IX describes the thiazolium salts and their numerous cyanine dyes derivatives. The last chapter concerns the monocyclic selenazoles. [Pg.1]

Ethane is the simplest hydrocarbon that can have distinct conformations Two the stag gered conformation and the eclipsed conformation, deserve special mention and are illustrated with molecular models m Figure 3 1... [Pg.105]

The classification of hydrocarbons as aliphatic or aromatic took place m the 1860s when It was already apparent that there was something special about benzene toluene and their derivatives Their molecular formulas (benzene is CgHg toluene is C7Hj ) indicate that like alkenes and alkynes they are unsaturated and should undergo addition reac tions Under conditions m which bromine for example reacts rapidly with alkenes and alkynes however benzene proved to be inert Benzene does react with Bi2 m the pres ence of iron(III) bromide as a catalyst but even then addition isn t observed Substitu tion occurs instead ... [Pg.424]

When we say cycloheptatriene is not aromatic but cycloheptatrienyl cation is we are not comparing the stability of the two to each other Cycloheptatriene is a stable hydrocarbon but does not possess the special stability required to be called aromatic Cycloheptatrienyl cation although aromatic is still a carbocation and reasonably reac tive toward nucleophiles Its special stability does not imply a rock like passivity but rather a much greater ease of formation than expected on the basis of the Lewis struc ture drawn for it A number of observations indicate that cycloheptatrienyl cation is far more stable than most other carbocations To emphasize its aromatic nature chemists often write the structure of cycloheptatrienyl cation m the Robinson circle m a ring style... [Pg.457]

Huckels rule (Section 11 19) Completely conjugated planar monocyclic hydrocarbons possess special stability when... [Pg.1285]

Synthetic Rubbers. Synthetic rubbers are polymers with rubberlike characteristics that are prepared from dienes or olefins. Rubbers with special properties can also be prepared from other polymers, such as polyacrylates, fiuorinated hydrocarbons, and polyurethanes. [Pg.1007]

Solutions. To dehver a spray, the formulated aerosol product should be as homogeneous as possible. That is, the active ingredients, the solvent, and the propellant should form a solution. Because the widely used halocarbon and hydrocarbon propellants do not always have the desired solubiUty characteristics for all the components in the product concentrate, special formulating techniques using solvents such as alcohols (qv), acetone (qv), and glycols (qv), are employed. [Pg.345]

The extremely nonpolar character of PFCs and very low forces of attraction between PFC molecules account for their special properties. Perfluorocarbons bod only slightly higher than noble gases of similar molecular weight, and their solvent properties are much more like those of argon and krypton than hydrocarbons (2). The physical properties of some PFCs are Hsted in Table 1. [Pg.282]

Fluorocarbons are made commercially also by the electrolysis of hydrocarbons in anhydrous hydrogen fluoride (Simons process) (14). Nickel anodes and nickel or steel cathodes are used. Special porous anodes improve the yields. This method is limited to starting materials that are appreciably soluble in hydrogen fluoride, and is most useflil for manufacturing perfluoroalkyl carboxyflc and sulfonic acids, and tertiary amines. For volatile materials with tittle solubility in hydrofluoric acid, a complementary method that uses porous carbon anodes and HF 2KF electrolyte (Phillips process) is useflil (14). [Pg.283]

Distinctions between tar sands bitumens and heavy oils are based largely on differences in viscosities. The bitumen in oil sand has a specific gravity of less than 0.986 g/mL (12°API), and thus oil sands may be regarded as a source of extremely heavy cmde oil. Whereas heavy oils might be produced by the same techniques used for the lighter cmde oils, the bitumens in tar sands are too viscous for these techniques. Consequently these oil-bearing stones have to be mined and specially processed to recover contained hydrocarbon. [Pg.96]

Absorber oil units offer the advantage that Hquids can be removed at the expense of only a small (34—69 kPa (4.9—10.0 psi)) pressure loss in the absorption column. If the feed gas is available at pipeline pressure, then Httle if any recompression is required to introduce the processed natural gas into the transmission system. However, the absorption and subsequent absorber-oil regeneration process tends to be complex, favoring the simpler, more efficient expander plants. Separations using soHd desiccants are energy-intensive because of the bed regeneration requirements. This process option is generally considered only in special situations such as hydrocarbon dew point control in remote locations. [Pg.172]

Knocking Characteristics of Pure Hydrocarbons, ASTM Special Pubhcation No. 225, American Society of Testing Materials, Philadelphia, 1958. [Pg.196]

Hydrocarbons. Synthesized hydrocarbons are the most popular of the synthetic base stocks. These are pure hydrocarbons (qv) and are manufactured from raw materials derived from cmde oil. Three types are used olefin oligomers, alkylated aromatics, and polybutenes. Other types, such as cycloahphatics, are also used in small volumes in specialized apphcations. [Pg.264]


See other pages where Hydrocarbons special is mentioned: [Pg.430]    [Pg.256]    [Pg.1693]    [Pg.7]    [Pg.1687]    [Pg.359]    [Pg.430]    [Pg.256]    [Pg.1693]    [Pg.7]    [Pg.1687]    [Pg.359]    [Pg.2377]    [Pg.2785]    [Pg.2806]    [Pg.8]    [Pg.4]    [Pg.118]    [Pg.329]    [Pg.423]    [Pg.24]    [Pg.163]    [Pg.283]    [Pg.431]    [Pg.195]    [Pg.312]    [Pg.264]    [Pg.357]    [Pg.384]    [Pg.388]    [Pg.389]   


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