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Fractionator propylene/propane

Studiengesselschaft Kohle m.b.H. (2) reported the effect of temperature on solubility level in supercritical gas. The solubility is highest within 20 K of the critical temperature and decreases as temperature is raised to 100 K above the critical temperature. At temperatures near the critical temperature, a sharp rise in solubility occurs as the pressure is increased to the vicinity of the critical pressure and increases further as the pressure is further increased. Less volatile materials are taken up to a lesser extent than more volatile materials, so the vapor phase has a different solute composition than the residual material. There does not seem to be substantial heating or cooling effects upon loading of the supercritical gas. It is claimed that the chemical nature of the supercritical gas is of minor importance to the phenomenon of volatility amplification. Ethylene, ethane, carbon dioxide, nitrous oxide, propylene, propane, and ammonia were used to volatilize hydrocarbons found in heavy petroleum fractions. [Pg.222]

Figure 8-53 shows a propylene-propane fractionator controlled at maximum boil-up by the differential pressure controller (DPC) across the trays. This loop is fast enough to reject upsets in the temperature... [Pg.42]

In the fractionation section, propane that accompanies the propylene feedstock is recovered as LPG product from the overhead of the depropanizer column (2), unreacted benzene is recovered from the overhead of the benzene column (4) and cumene product is taken as overhead from the cumene column (5). Di-isopropylbenzene (DIPB) is recovered in the overhead of the DIPB column (6) and recycled to the transalkylation reactor (3) where it is transalkylated with benzene over a second zeolite catalyst to produce additional cumene. A small quantity of heavy byproduct is recovered from the bottom of the DIPB column (6) and is typically blended to fuel oil. The cumene product has a high purity (99.96-99.97 wt%), and cumene yields of 99.7 wt% and higher are achieved. [Pg.49]

At atmospheric pressure, what is the fraction of propane converted to propylene at 400, 500, and 600°C if equilibrium is reached at each temperature Assume ideal behavior. [Pg.45]

Where xcs xc3, and xo2 are the mole fractions of propane, propylene, and oxygen in the gas phase, kc3°, kacr. and kcox are the rate constants of propylene, acrolein, and COx production, Kc3" is a propylene adsorption constant, and (O2) denotes the zero order oxygen dependence. [Pg.362]

Fractionation data are shown in table 9.8 for EMAgoMo fractionated with propane first and then with propylene at 130°C. Propane is only able to extract 31% of the copolymer charged to the fractionation columns. The polydisper-sities of the first six fractions are less than that of the parent material and the concentration of methyl acrylate in the backbone of the fractions is only about 0.5 wt% less than that of the parent material. [Pg.209]

Charts containing plots of log K vs. log P for each of several convergence pressures are presented in the Engineering Data Book.19 Charts are presented for nitrogen, methane, ethylene, ethane, propylene, propane, i-butane, n-butane, /-pentane, n-pentane, hexane, octane, decane, hydrogen sulfide, selected binaries, and the normal boiling fractions. [Pg.533]

Tsitsishvili et al. have carried out experiments of methanol conversion on H-offretite and TMA-offretite. TMA-offretite zeolites were calcined at 200 and 450 °C. H-offretite zeolites were prepared by ammonium ion-exchange and then calcined at 300 and 450 C. TMA-offretite calcined at 200 C was inactive, probably because the channels are blocked by the large Me N ions so that the acid sites become inaccessible for methanol molecules. A hydrocarbon fraction containing principally propylene, propane, n-butane, and n-butene was obtained in the cases of TMA-offretite and H-offretite calcined at 450 "C. At reaction temperatures lower than 210 C only dimethyl ether was detected. H-offretite zeolites are active in the isomerization of xylenes, indicating that the removal of TMA-cations enlarged the pore opening. [Pg.10]

C3S from the dual pressure depropanizer system are combined and may require further hydrogenation to remove methyl acetylene and propadiene (10). Either polymer-grade or chemical-grade propylene can be produced overhead from a propylene-propane fractionator. The propyl-... [Pg.129]

Permeate composition (mole fraction) Propylene = 0.9877, Propane = 0.0122 and Isobutane = 0.0001... [Pg.312]

Butane and propane (with other hydrocarbons in the paraffin series) are recovered from wet natural gas, from natural gas associated with or dissolved in crude oil, and from petroleum refinery gases. They may be separated from wet natural gas or crude oil through absorption in light mineral seal oil, through adsorption on surfaces such as activated charcoal, or by refrigeration, followed in each case by fractionation. Propylene and other gases in the monoolefin series are recovered from petroleum gases by fractionation. [Pg.459]

Partial recycle of propylene-propane mix. The propane in the feed would increase. This decreases the concentrations of the reactants and reduces the production of cumene. The superficial velocity in the reactor would increase. This reduces residence time and the fraction bypassed in the fluidized bed. [Pg.679]

Increasing system temperature Increasing system pressure Increasing benzene mole fraction Increasing propylene mole fraction Increasing propane mole fraction Increasing cumene mole fraction Increasing DIPB mole fraction... [Pg.687]

Though offering good olefin/paraffin separation performances at laboratory scale, those materials were subject to a loss of solvent by evaporation, which resulted in dramatic fall of olefin/paraffin separation performances. In order to maintain the separation performances of those membranes, the feed had thus to be saturated with vapor in order to prevent the drying of the membrane. This is a critical point as, at industrial scale, propylene/propane mixtures are dehydrated before being fractionated by distillation. [Pg.197]

The advantages of coupling a permeation membrane on a distillation-based propylene/propane fractionation were first evaluated in a study carried out at University of Colorado, Boulder, and sponsored by BP. Various membrane/ distillation coupling scenarios (membrane unit located on the top stream or on the bottom stream or on the side stream of the column, all cases with a recirculation of the propylene-enriched permeate inside the column) were compared with a reference case based on a propylene/propane splitter column operated with 152 theoretical stages, a reflux ratio equal to 24.1 and a feed... [Pg.199]

Liquefied gas fractions (propane, propylene, butanes, butenes) that will be able to provide feedstocks to units of MTBE, ETBE, alkylation, dimerization, polymerization after sweetening and/or selective hydrogenation. [Pg.385]

Olefins are produced primarily by thermal cracking of a hydrocarbon feedstock which takes place at low residence time in the presence of steam in the tubes of a furnace. In the United States, natural gas Hquids derived from natural gas processing, primarily ethane [74-84-0] and propane [74-98-6] have been the dominant feedstock for olefins plants, accounting for about 50 to 70% of ethylene production. Most of the remainder has been based on cracking naphtha or gas oil hydrocarbon streams which are derived from cmde oil. Naphtha is a hydrocarbon fraction boiling between 40 and 170°C, whereas the gas oil fraction bods between about 310 and 490°C. These feedstocks, which have been used primarily by producers with refinery affiliations, account for most of the remainder of olefins production. In addition a substantial amount of propylene and a small amount of ethylene ate recovered from waste gases produced in petroleum refineries. [Pg.171]

Because of the low relative volatiHty, fractionation of propylene and propane is even more difficult than the fractionation of ethylene and ethane. [Pg.441]

The propylene fractionator operates at a pressure of 1.8 to 2.0 MPa with more than 160 trays required for a high purity propylene product. Often a two-tower design is employed when polymer grade (99.5%+) is required. A pasteurization section may also be used when high purity is required. The bottoms product contains mainly propane that can be recycled to the cracking heaters or used as fuel. Typical tower dimensions and internals for a 450,000 t/yr ethylene plant with naphtha feed are summarized in Table 7. [Pg.441]


See other pages where Fractionator propylene/propane is mentioned: [Pg.2984]    [Pg.2984]    [Pg.747]    [Pg.248]    [Pg.571]    [Pg.249]    [Pg.264]    [Pg.248]    [Pg.265]    [Pg.136]    [Pg.74]    [Pg.751]    [Pg.332]    [Pg.289]    [Pg.1107]    [Pg.248]    [Pg.482]    [Pg.454]    [Pg.259]    [Pg.193]    [Pg.203]    [Pg.662]    [Pg.175]    [Pg.46]    [Pg.128]    [Pg.94]    [Pg.10]   
See also in sourсe #XX -- [ Pg.259 ]




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