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Hydrocarbons transfer

The best evidence of hydrocarbon transfer into cells is with oocytes. Oocyte development in cockroaches, as in most oviparous animals, is characterized by a dramatic growth period during which all maternally derived macromolecules are sequestered. Vitellogenin uptake by the oocyte has been extensively studied... [Pg.307]

The values of transfer constants directly indicate the danger of unfounded estimates of radical reactivities with respect to various substrates. The ratio of transfer rates of polystyrene and poly(methyl methacrylate) radicals to various substrates assumes a range of values [38] which are dependent on the substrate properties. The former radical is more reactive towards mercaptans, CBr4 or CC14, and the latter towards hydrocarbon transfer agents and trialkylamines which assume donor character in the transition complex. The interpretation of polar effects in macroradical reactivities is not yet satisfactory. [Pg.457]

In view of the fact that the water content in the bottoms product of the pressurized column is twice that of the prerun column, the hydrocarbons transferred ftom the prerun column into the pressurized column will reliably be found in the bottoms product, i.e. they are transferred to the atmospheric distillation column. Thus, ethanol becomes the key component for the pressurized column. Since the bottom product of the pressurized column - unlike that of the atmospheric column - does nOt have to meet certain purity requirements, this column need not have a side outlet for ethanol, but the ethanol is quantitatively transferred to the atmospheric columit. The high methanol content in the bottom of the pressurized column facilitates ethanol separation. Nevertheless, for the same number of trays, the pressurized operation of this column leads to a higher reflux than in the atmospheric column. The bottoms product ftom the pressurized column is transferred to the atmospheric column at approximately 125-35°C. The overhead product is obtained at approximately 115-125°C, condensed in the reboiler of the atmospheric column, and fed to the reflux drum of the pressurized column. From there, some of the overhead product is withdrawn by way of an after-cooler as on-spec methanol while the rest is pumped back uncooled as reflux to the column head. [Pg.142]

Figure 16.13 ETFE lined composite tubing for hydrocarbon transfer. (Courtesy Pilot Industries and DuPont Companies.)... Figure 16.13 ETFE lined composite tubing for hydrocarbon transfer. (Courtesy Pilot Industries and DuPont Companies.)...
Its charge transfer complexes with aromatic hydrocarbons have characteristic melting points and may be used for the identification and purification of the hydrocarbons. [Pg.406]

Liquid viscosity is one of the most difficult properties to calculate with accuracy, yet it has an important role in the calculation of heat transfer coefficients and pressure drop. No single method is satisfactory for all temperature and viscosity ranges. We will distinguish three cases for pure hydrocarbons and petroleum fractions ... [Pg.126]

Williams R M, Koeberg M, Lawson J M, An Y-Z, Rubin Y, Paddon-Row M N and Verhoeven J W 1996 Photoinduced electron transfer to Cgg across extended 3- and 11 a-bond hydrocarbon bridges creation of a long-lived charge-separated state J. Org. Chem. 61 5055-62... [Pg.2435]

Like bromine, iodine is soluble in organic solvents, for example chloroform, which can be used to extract it from an aqueous solution. The iodine imparts a characteristic purple colour to the organic layer this is used as a test for iodine (p. 349). NB Brown solutions are formed when iodine dissolves in ether, alcohol, and acetone. In chloroform and benzene a purple solution is formed, whilst a violet solution is produced in carbon disulphide and some hydrocarbons. These colours arise due to charge transfer (p. 60) to and from the iodine and the solvent organic molecules. [Pg.320]

Organohthium and organomagnesium compounds are stable species when prepared m suitable solvents such as diethyl ether They are strongly basic however and react instantly with proton donors even as weakly acidic as water and alcohols A proton is transferred from the hydroxyl group to the negatively polarized carbon of the organometallic compound to form a hydrocarbon... [Pg.592]

Fig. 20. Proposed photochemical mechanisms for the generation of acid from sulfonium salt photolysis. Shown ate examples illustrating photon absorption by the onium salt (direct irradiation) as well as electron transfer sensitization, initiated by irradiation of an aromatic hydrocarbon. Fig. 20. Proposed photochemical mechanisms for the generation of acid from sulfonium salt photolysis. Shown ate examples illustrating photon absorption by the onium salt (direct irradiation) as well as electron transfer sensitization, initiated by irradiation of an aromatic hydrocarbon.
In production, anhydrous formaldehyde is continuously fed to a reactor containing well-agitated inert solvent, especially a hydrocarbon, in which monomer is sparingly soluble. Initiator, especially amine, and chain-transfer agent are also fed to the reactor (5,16,17). The reaction is quite exothermic and polymerisation temperature is maintained below 75°C (typically near 40°C) by evaporation of the solvent. Polymer is not soluble in the solvent and precipitates early in the reaction. [Pg.58]

Fuel-fired furnaces primarily utilize carbonaceous or hydrocarbon fuels. Since the purpose of a furnace is to generate heat for some useful appHcation, flame temperature and heat transfer are important aspects of furnace design. Heat transfer is impacted by the flame emissivity. A high emissivity means strong radiation to the walls. [Pg.141]


See other pages where Hydrocarbons transfer is mentioned: [Pg.356]    [Pg.81]    [Pg.87]    [Pg.297]    [Pg.289]    [Pg.146]    [Pg.492]    [Pg.20]    [Pg.165]    [Pg.101]    [Pg.568]    [Pg.356]    [Pg.81]    [Pg.87]    [Pg.297]    [Pg.289]    [Pg.146]    [Pg.492]    [Pg.20]    [Pg.165]    [Pg.101]    [Pg.568]    [Pg.264]    [Pg.313]    [Pg.406]    [Pg.611]    [Pg.203]    [Pg.560]    [Pg.2582]    [Pg.2804]    [Pg.239]    [Pg.512]    [Pg.513]    [Pg.23]    [Pg.127]    [Pg.165]    [Pg.593]    [Pg.594]    [Pg.528]    [Pg.124]    [Pg.208]    [Pg.167]    [Pg.278]    [Pg.466]    [Pg.266]    [Pg.363]    [Pg.394]    [Pg.396]   
See also in sourсe #XX -- [ Pg.39 ]




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