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Olefin paraffin alkylation

Olefin/Paraffin Alkylation Evolution of a Green Technology... [Pg.475]

Figure 12.1 Conceptual mechanism for olefin/paraffin alkylation [10],... Figure 12.1 Conceptual mechanism for olefin/paraffin alkylation [10],...
In a polluted or urban atmosphere, O formation by the CH oxidation mechanism is overshadowed by the oxidation of other VOCs. Seed OH can be produced from reactions 4 and 5, but the photodisassociation of carbonyls and nitrous acid [7782-77-6] HNO2, (formed from the reaction of OH + NO and other reactions) are also important sources of OH ia polluted environments. An imperfect, but useful, measure of the rate of O formation by VOC oxidation is the rate of the initial OH-VOC reaction, shown ia Table 4 relative to the OH-CH rate for some commonly occurring VOCs. Also given are the median VOC concentrations. Shown for comparison are the relative reaction rates for two VOC species that are emitted by vegetation isoprene and a-piuene. In general, internally bonded olefins are the most reactive, followed ia decreasiag order by terminally bonded olefins, multi alkyl aromatics, monoalkyl aromatics, C and higher paraffins, C2—C paraffins, benzene, acetylene, and ethane. [Pg.370]

PMMA is not affected by most inorganic solutions, mineral oils, animal oils, low concentrations of alcohols paraffins, olefins, amines, alkyl monohahdes and ahphatic hydrocarbons and higher esters, ie, >10 carbon atoms. However, PMMA is attacked by lower esters, eg, ethyl acetate, isopropyl acetate aromatic hydrocarbons, eg, benzene, toluene, xylene phenols, eg, cresol, carboHc acid aryl hahdes, eg, chlorobenzene, bromobenzene ahphatic acids, eg, butyric acid, acetic acid alkyl polyhaHdes, eg, ethylene dichloride, methylene chloride high concentrations of alcohols, eg, methanol, ethanol 2-propanol and high concentrations of alkahes and oxidizing agents. [Pg.262]

Paraffin alkylation as discussed here refers to the addition reaction of an isoparaffin and an olefin. The desired product is a higher molecular weight paraffin that exhibits a greater degree of branching than either of the reactants. [Pg.45]

Although the alkylation of paraffins can be carried out thermally (3), catalytic alkylation is the basis of all processes in commercial use. Early studies of catalytic alkylation led to the formulation of a proposed mechanism based on a chain of ionic reactions (4—6). The reaction steps include the formation of a light tertiary cation, the addition of the cation to an olefin to form a heavier cation, and the production of a heavier paraffin (alkylate) by a hydride transfer from a light isoparaffin. This last step generates another light tertiary cation to continue the chain. [Pg.45]

When CH3OH is adsorbed first, the strongly adsorbed CH OH is transformed into ethers, olefins, paraffins and aromatics, m a similar way, when it was the only reactant present (7) (A). C2H4 remains inactive below 623 K. At this temperature, it begins to react as it is shown by the NMR signals in the paraffinic region (B). It can be assumed that in such conditions, ethylene alkylates aromatics obtained from methanol. [Pg.120]

Paraffin alkylation involves the add-catalyzed addihon of an olefin to a branched paraffin to give a highly branched, paraffinic product The representahve reaction is that of isobutane with 2-butene to give 2,2,4-trimethylpentane ... [Pg.508]

Development of processes of dehydrogenate -paraffin to -olefins and alkylate benzene with them (mid-1960s) Isomerization of Cg aromatics to /7-xylene (late 1950s) Adsorptive separation of /7-xylene in high yield and purity, making possible separation of other isomers by precise fractionation (early 1970s)... [Pg.1260]

To conclude this section, it is necessary to state that besides their application in catalytic cracking, amorphous silica-alumina acid catalysts have been applied in other hydrocarbon transformations, such as isomerization of olefins, paraffins, and alkyl aromatics, the alkylation of aromatics with alcohols and olefins, and in olefin oligomerization [55],... [Pg.429]

Description Linear paraffins are fed to a Pacol reactor (1) to dehydrogenate the feed into corresponding linear olefins. Reactor effluent is separated into gas and liquid phases in a separator (2). Diolefins in the separator liquid are selectively converted to mono-olefins in a DeFine reactor (3). Light ends are removed in a stripper (4) and the resulting olefin-paraffin mixture is sent to a Detal reactor (5) where the olefins are alkylated with benzene. The reactor effluent is sent to a fractionation section (6, 7) for separation and recycle of unreacted benzene to the Detal reactor, and separation and recycle of unreacted paraffins to the Pacol reactor. A rerun column (8) separates the LAB product from the heavy alkylate bottoms stream. [Pg.7]

Figure 2.4 Species-specific evolution profiles for (a) paraffin (b) olefin (c) alkyl aromatic products obtained when a PE-HZSM-5 sample was heated. (Reproduced by permission of John Wiley Sons, Ltd)... Figure 2.4 Species-specific evolution profiles for (a) paraffin (b) olefin (c) alkyl aromatic products obtained when a PE-HZSM-5 sample was heated. (Reproduced by permission of John Wiley Sons, Ltd)...
Figure 2.4 shows species-specific evolution profiles for paraffin, olefin, and alkyl aromatic volatile products formed by heating the PE-HZSM-5 sample. The numbers in parentheses denote the number of isomers detected. The volatile product slates for the PE-HZSM-5 sample reflect that C3-C5 hydrocarbons were the dominant species formed. The temperature corresponding to the maximum paraffin and olefin evolution rates was 280°C, whereas alkyl aromatic evolution maximized at 310°C. Below 200°C, volatile... [Pg.50]

Figure 2.9 shows the species-specific evolution profiles for (a) paraffin (b) olefin and (c) alkyl aromatic volatile products for the PE-PtHZSM-5 sample heated in hydrogen. As expected, paraffins dominated the hydrocracking volatile product slate and olefin and alkyl aromatic yields were greatly reduced compared with results obtained when the same sample was heated in helium. The paraffin profile for the PE-PtHZSM-5 sample heated in hydrogen exhibited two maxima. Below 200°C, volatile product mixtures were composed entirely of paraffins. As the sample temperature increased, a wide range of... [Pg.60]

There are several routes for the production of LAB. In most cases, a linear paraffin feedstock is used to produce olefins for alkylation. The paraffin feedstock is typically a mixture of linear paraffins in the range of C10-C14. The paraffins are derived from kerosene by means of adsorptive separation. [Pg.664]


See other pages where Olefin paraffin alkylation is mentioned: [Pg.476]    [Pg.617]    [Pg.404]    [Pg.476]    [Pg.617]    [Pg.404]    [Pg.353]    [Pg.441]    [Pg.441]    [Pg.52]    [Pg.197]    [Pg.27]    [Pg.17]    [Pg.61]    [Pg.33]    [Pg.510]    [Pg.510]    [Pg.68]    [Pg.15]    [Pg.16]    [Pg.50]    [Pg.370]    [Pg.1721]    [Pg.12]    [Pg.60]    [Pg.64]    [Pg.305]    [Pg.26]    [Pg.12]    [Pg.127]    [Pg.178]    [Pg.206]    [Pg.822]   
See also in sourсe #XX -- [ Pg.475 , Pg.476 , Pg.481 ]




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