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C-4 hydrocarbons

The above expressions are empirical approaches, with m and D. as parameters, for including an anliamionic correction in the RRKM rate constant. The utility of these equations is that they provide an analytic fomi for the anliamionic correction. Clearly, other analytic fomis are possible and may be more appropriate. For example, classical sums of states for Fl-C-C, F1-C=C, and F1-C=C hydrocarbon fragments with Morse stretching and bend-stretch coupling anhamionicity [M ] are fit accurately by the exponential... [Pg.1022]

D. B. Broughton and co-workers. The Separation of p-SCylenefrom C Hydrocarbon Mixtures by Parex Process, AIChE, Puerto Rico, May 1970. [Pg.425]

Solution Polymerization. Two solution polymerization technologies ate practiced. Processes of the first type utilize heavy solvents those of the second use molten PE as the polymerization medium (57). Polyethylene becomes soluble ia saturated C —hydrocarbons above 120—130°C. Because the viscosity of HDPE solutions rapidly iacrease with molecular weight, solution polymerization is employed primarily for the production of low mol wt resias. Solution process plants were first constmcted for the low pressure manufacture of PE resias ia the late 1950s they were later exteasively modified to make their operatioa economically competitive. [Pg.386]

Fig. 6. Boiling points of C —hydrocarbons. P, iso and normal paraffins C, C - and Cg-cycloparaffins and A, aromatics. Fig. 6. Boiling points of C —hydrocarbons. P, iso and normal paraffins C, C - and Cg-cycloparaffins and A, aromatics.
A selection of industrial appHcations of extractive distillation includes (/) the separation of the / -butane—butadiene azeotrope in mixed C -hydrocarbon streams using furfural [98-01-17, as the solvent (36) (2) the dehydration of ethanol using ethylene glycol [107-21-1] (37—39) (J)... [Pg.185]

Since most of the C, hydrocarbons boil extremely close to isoprene, simple distillation of the C, cut would not produce high purity isoprene. Two stages of extractive distillation with acetonitrile are used where the ACN modifies the relative volatilities of the hydrocarbons and thus enables the separation to be made. [Pg.108]

Ochraroxm A PyTi. olizidinc alkaloids Kubracoxin B V<) 1 ari 1 c hydrocarbons (i<.is(flinc... [Pg.303]

Edmister, W. C., Hydrocarbon Absorption and Fractionar tion Process Design Methods, Pet. Engr. May 1947-March 1949 and, Absorption and Stripping—Factor Functions for Distillation Calculations by Manual and Digital—Computer Methods. A.I.ChJE. foumal, V. 3, No. 2 p. 165 (1957). [Pg.224]

Heat of combustion is the heat liberated or absorbed when one gram mole of the substance is completely oxidized to liquid water and CO2 gas at one atmosphere and 20°C or 25°C. (Cj-C hydrocarbons and cyclohexane at 25°C, others at 20°C). The gross heating value in Btu/ft could be calculated as follows ... [Pg.377]

The activation energy of polypropylene degradation was lowered with ferrierite catalyst. The yield of i-butene as well as the yield of olefin over ferrierite was higher than that over HZSM-5. In the case of liquid product, main product over ferrierite is C hydrocarbon, while products were distributed over mainly C -C over HZSM-5. The amount of gaseous product increased with increasing ferrierite/PP ratio. Ferrierite showed high catalytic stability for the polypropylene degradation. [Pg.320]

Sulfuric acid, Sulfur trioxide Vervalin, H. C., Hydrocarbon Process., 1976, 55(9), 323 Dining sulfonation of 4-nitrotoluene at 32° C with 24% oleum in a 2000 1 vessel, a runaway decomposition reaction set in and ejected the contents as a carbonaceous mass. The thermal decomposition temperature was subsequently estimated as 52°C (but see above). [Pg.910]

Figure 11.6 Total ion current pyrogram obtained from 30 jig of bleached beeswax with a resistively heatedpyrolyser at 800°C. FA, fatty acid F C, hydrocarbon X Y, chain length X with Y double bonds. Reprinted from J. Anal. Appl. Pyrol., 50, Asperger et al., 2, 13, Copyright 1999 with permission from Elsevier... Figure 11.6 Total ion current pyrogram obtained from 30 jig of bleached beeswax with a resistively heatedpyrolyser at 800°C. FA, fatty acid F C, hydrocarbon X Y, chain length X with Y double bonds. Reprinted from J. Anal. Appl. Pyrol., 50, Asperger et al., 2, 13, Copyright 1999 with permission from Elsevier...
Exchange broadening, see Electron paramagnetic response spectroscopy Exchange-coorelation effects, 34 213 Exchange reactions, 26 711-279, 31 106-107 on alloys, 26 294—296 carbon-14, from benzene- C to C - hydrocarbons, 23 127... [Pg.103]

Crude oil desalting Heater stack gas (CO, SO, NO c, hydrocarbons, and particulates), fugitive emissions (hydrocarbons) Crnde oil/desalter slndge (iron rnst, clay, sand, water, emnlsified oil and wax, metals)... [Pg.88]

C) Hydrocarbon fuels when combusted under actual (nonideal) combustion conditions produce several intermediate products in addition to carbon dioxide and water and include the unbumed hydrocarbon, carbon monoxide, oxides of nitrogen, hydroxyl radicals, and the hydrogen ions. [Pg.255]

As can be seen in Table III the Synthol process produces a large amount of C to C- hydrocarbons which are predominantly olefins. At Sasol tne C stream from the cryogenic separation unit is fed to a standard ethylene plant. The feed is first dried and then fractionated to remove the small amounts of C-. and C products. The C stream is then selectively hydrogenated to remove acetylene... [Pg.29]


See other pages where C-4 hydrocarbons is mentioned: [Pg.302]    [Pg.406]    [Pg.333]    [Pg.556]    [Pg.370]    [Pg.250]    [Pg.282]    [Pg.166]    [Pg.506]    [Pg.314]    [Pg.432]    [Pg.482]    [Pg.504]    [Pg.472]    [Pg.108]    [Pg.43]    [Pg.160]    [Pg.664]    [Pg.125]    [Pg.195]    [Pg.279]    [Pg.23]    [Pg.53]    [Pg.51]    [Pg.89]    [Pg.95]    [Pg.118]    [Pg.55]    [Pg.3]    [Pg.118]    [Pg.188]    [Pg.28]   


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Analogs with C-methyl (and Other Hydrocarbon) Substituents in the Piperidine Ring

Homodimerization of Hydrocarbons via Palladium-Promoted C—H Activation

Hydrocarbons, hydrocarbon s. C-Carbalkoxylation

Hydrocarbons, hydrocarbon s. C-Carboxylation

Ramsden, C. A., Heterocyclic: Betaine Derivatives of Alternant Hydrocarbons

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