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Internal hydrocarbons

The eggs of B. germanica contain the same types of hydrocarbons as the hemolymph, HDLp, and cuticle of the adult female. Only 150 pg of hydrocarbons accumulate on the epicuticular surface whereas up to 450 pg accumulate within the female during the period of egg maturation (Fan et al., 2002). The internal hydrocarbons are divided primarily between the ovaries, fat body, and 150 pg of HDLp-bound hydrocarbons in the hemolymph. During oocyte maturation ovarian hydrocarbons increase by more than 65-fold - from 3.5 pg on day-1 to 232 pg on day-8 (Fan et al., 2002). However, after oviposition on day-9, ovarian hydrocarbons decline to only 8.2 pg, demonstrating that hydrocarbons were associated with the ovulated oocytes. Radiotracing results indicate that they serve as components of the cuticular lipids of the embryos and first instars (Fan and Schal, unpublished results). [Pg.308]

These studies show that for T. ni and S. eridania, the internal hydrocarbon found in the insect immediately prior to a molt (larva to larva, larva to pupa and pupa to adult) is used as both cuticular and internal hydrocarbon immediately after the molt. The cast skin contains all the hydrocarbons that were found on the surface of the insect prior to the molt, indicating that the cuticular hydrocarbons were not re-adsorbed and re-utilized. Rather, the cuticular hydrocarbons of the newly ecdysed insect are from those synthesized and stored during the previous stage. [Pg.46]

Hamilton, R. J. and Service, M. W. (1983). Value of cuticular and internal hydrocarbons for the identification of larvae of Anopheles gambiae Giles, Anopheles arabiensis Patton and Anopheles melas Theobald. Ann. Prop. Med. Parasitol., 77, 203-210. [Pg.154]

ISO 834 (hydrocarbon time/ temperature curve) International Hydrocarbon fire developed in the early 1970s [94]... [Pg.149]

After the column was lined out, liquid samples were taken from the butenes condenser and from the reboiler. The composition of these samples served as a guide to indicate which adjustments in operating conditions were necessary to obtain the desired column operation. If the reboiler liquid contained 1-butene or isobutene, its temperature was increased, provided there was no butadiene in the overhead. If butadiene appeared in the overhead, the internal hydrocarbon reflux was increased by increasing the pressure or decreasing the solvent feed tray temperature. Solvent-to-hydrocarbon feed rate adjustments were also effective in giving desired changes in bottoms and overhead compositions. [Pg.228]

Determined by GLC analysis using n-dodecane as an internal hydrocarbon standard. All products were characterized by IR. NMR and HRMS. [Pg.1115]

As seen in Chapter 2, mixtures of hydrocarbons and petroleum fractions are analyzed in the laboratory using precise standards published by ASTM (American Society for Testing and Materials) and incorporated for the most part into international (ISO), European (EN) and national (NF) collections. We wiil recall below the methods utilizing a classification by boiling point ... [Pg.98]

The thennalization stage of this dissociation reaction is not amenable to modelling at the molecular dynamics level becanse of the long timescales required. For some systems, snch as O2 /Pt(l 11), a kinetic treatment is very snccessfiil [77]. However, in others, thennalization is not complete, and the internal energy of the molecnle can still enliance reaction, as observed for N2 /Fe(l 11) [78, 79] and in tlie dissociation of some small hydrocarbons on metal snrfaces [M]- A detailed explanation of these systems is presently not available. [Pg.913]

To act as an international center of hydrocarbon chemistry and to facilitate exchange of information and ideas through visits of scientists, col-loquia, and research symposia... [Pg.125]

Hydrocarbons that contain a carbon-carbon triple bond are called alkynes Non cyclic alkynes have the molecular formula C H2 -2 Acetylene (HC=CH) is the simplest alkyne We call compounds that have their triple bond at the end of a carbon chain (RC=CH) monosubstituted or terminal alkynes Disubstituted alkynes (RC=CR ) have internal triple bonds You will see m this chapter that a carbon-carbon triple bond is a functional group reacting with many of the same reagents that react with the double bonds of alkenes... [Pg.363]

Troost and Olavesen investigated the application of an internal standardization to the quantitative analysis of polynuclear aromatic hydrocarbons. The following results were obtained for the analysis of the analyte phenanthrene using isotopically labeled phenanthrene as an internal standard... [Pg.133]

Fig. 6. Schematic ignition diagram for a hydrocarbon+ O2 mixture, with appHcations. Region A, very rapid combustion, eg, a jet engine region B, low temperature ignition, eg, internal combustion engine, safety ha2ards regions C and D, slow oxidation to useful chemicals, eg, 0-heterocycHc compounds in C and alcohols and peroxides in D. Courtesy of Blackwell Scientific PubHcations, Ltd., Oxford (60). Fig. 6. Schematic ignition diagram for a hydrocarbon+ O2 mixture, with appHcations. Region A, very rapid combustion, eg, a jet engine region B, low temperature ignition, eg, internal combustion engine, safety ha2ards regions C and D, slow oxidation to useful chemicals, eg, 0-heterocycHc compounds in C and alcohols and peroxides in D. Courtesy of Blackwell Scientific PubHcations, Ltd., Oxford (60).
M. Castegnaro, M. Coombs, M. A. PhiUipson, M. C. Bourgade, andj. Michelon, the 7th Polynuclear Aromatic Hydrocarbons, International Symposium, BateUe Press, Columbus, Ohio, 1982, pp. 257—268. [Pg.532]

SASOL. SASOL, South Africa, has constmcted a plant to recover 50,000 tons each of 1-pentene and 1-hexene by extractive distillation from Fischer-Tropsch hydrocarbons produced from coal-based synthesis gas. The company is marketing both products primarily as comonomers for LLDPE and HDPE (see Olefin polymers). Although there is still no developed market for 1-pentene in the mid-1990s, the 1-hexene market is well estabhshed. The Fischer-Tropsch technology produces a geometric carbon-number distribution of various odd and even, linear, branched, and alpha and internal olefins however, with additional investment, other odd and even carbon numbers can also be recovered. The Fischer-Tropsch plants were originally constmcted to produce gasoline and other hydrocarbon fuels to fill the lack of petroleum resources in South Africa. [Pg.440]

PGM catalyst technology can also be appHed to the control of emissions from stationary internal combustion engines and gas turbines. Catalysts have been designed to treat carbon monoxide, unbumed hydrocarbons, and nitrogen oxides in the exhaust, which arise as a result of incomplete combustion. To reduce or prevent the formation of NO in the first place, catalytic combustion technology based on platinum or palladium has been developed, which is particularly suitable for appHcation in gas turbines. Environmental legislation enacted in many parts of the world has promoted, and is expected to continue to promote, the use of PGMs in these appHcations. [Pg.173]

The atoms and molecules at the interface between a Hquid (or soHd) and a vacuum are attracted more strongly toward the interior than toward the vacuum. The material parameter used to characterize this imbalance is the interfacial energy density y, usually called surface tension. It is highest for metals (<1 J/m ) (1 J/m = N/m), moderate for metal oxides (<0.1 J/m ), and lowest for hydrocarbons and fluorocarbons (0.02 J /m minimum) (4). The International Standards Organization describes weU-estabHshed methods for determining surface tension, eg, ISO 304 for Hquids containing surfactants and ISO 6889 for two-Hquid systems containing surfactants. [Pg.541]

Monohydroxyaluminum distearate, (HO)Al(OOC(CH2) gCH2)2, used to be the largest selling aluminum carboxylate (1). Although stiU sold, the product is no longer Hsted in the U.S. International Trade Commission Report (1) because of low volume or confidentiahty constraints because of too few supphers. Aluminum distearate is a white powder that is insoluble in water, alcohol, and ether. A key property is its abiUty to gel vegetable oils and hydrocarbons. Aluminum distearate is prepared by the reaction of aqueous sodium stearate with aqueous aluminum sulfate or chloride at pH 7.3. Aluminum monostearate is formed if the sodium stearate solution is held at pH 9.5 (44). [Pg.143]


See other pages where Internal hydrocarbons is mentioned: [Pg.314]    [Pg.45]    [Pg.46]    [Pg.77]    [Pg.78]    [Pg.314]    [Pg.208]    [Pg.317]    [Pg.307]    [Pg.130]    [Pg.314]    [Pg.45]    [Pg.46]    [Pg.77]    [Pg.78]    [Pg.314]    [Pg.208]    [Pg.317]    [Pg.307]    [Pg.130]    [Pg.331]    [Pg.268]    [Pg.316]    [Pg.113]    [Pg.133]    [Pg.345]    [Pg.421]    [Pg.171]    [Pg.579]    [Pg.87]    [Pg.396]    [Pg.357]    [Pg.364]    [Pg.366]    [Pg.453]    [Pg.184]    [Pg.202]    [Pg.242]    [Pg.162]    [Pg.235]    [Pg.1]    [Pg.228]   
See also in sourсe #XX -- [ Pg.46 , Pg.77 , Pg.78 , Pg.154 ]




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