Propane saturation

Alkanes. The saturated open-chain (acyclic) hydrocarbons (C H2 +2) have names ending in -ane. The first four members have the trivial names methane (CH4), ethane (CH3CH3 or C2H5), propane (C3H8), and butane (C4Hjo). For the remainder of the alkanes, the first portion of the name... 

Many simple systems that could be expected to form ideal Hquid mixtures are reasonably predicted by extending pure-species adsorption equiUbrium data to a multicomponent equation. The potential theory has been extended to binary mixtures of several hydrocarbons on activated carbon by assuming an ideal mixture (99) and to hydrocarbons on activated carbon and carbon molecular sieves, and to O2 and N2 on 5A and lOX zeoHtes (100). Mixture isotherms predicted by lAST agree with experimental data for methane + ethane and for ethylene + CO2 on activated carbon, and for CO + O2 and for propane + propylene on siUca gel (36). A statistical thermodynamic model has been successfully appHed to equiUbrium isotherms of several nonpolar species on 5A zeoHte, to predict multicomponent sorption equiUbria from the Henry constants for the pure components (26). A set of equations that incorporate surface heterogeneity into the lAST model provides a means for predicting multicomponent equiUbria, but the agreement is only good up to 50% surface saturation (9). 

Irradiation of ethyleneimine (341,342) with light of short wavelength ia the gas phase has been carried out direcdy and with sensitization (343—349). Photolysis products found were hydrogen, nitrogen, ethylene, ammonium, saturated hydrocarbons (methane, ethane, propane, / -butane), and the dimer of the ethyleneimino radical. The nature and the amount of the reaction products is highly dependent on the conditions used. For example, the photoproducts identified ia a fast flow photoreactor iacluded hydrocyanic acid and acetonitrile (345), ia addition to those found ia a steady state system. The reaction of hydrogen radicals with ethyleneimine results ia the formation of hydrocyanic acid ia addition to methane (350). Important processes ia the photolysis of ethyleneimine are nitrene extmsion and homolysis of the N—H bond, as suggested and simulated by ab initio SCF calculations (351). The occurrence of ethyleneimine as an iatermediate ia the photolytic formation of hydrocyanic acid from acetylene and ammonia ia the atmosphere of the planet Jupiter has been postulated (352), but is disputed (353). 

Thermal polymerization is not as effective as catalytic polymerization but has the advantage that it can be used to polymerize saturated materials that caimot be induced to react by catalysts. The process consists of the vapor-phase cracking of, for example, propane and butane, followed by prolonged periods at high temperature (510—595°C) for the reactions to proceed to near completion. Olefins can also be conveniendy polymerized by means of an acid catalyst. Thus, the treated olefin-rich feed stream is contacted with a catalyst, such as sulfuric acid, copper pyrophosphate, or phosphoric acid, at 150—220°C and 1035—8275 kPa (150—1200 psi), depending on feedstock and product requirement. 

FeedSa.tura.tlon, When gas feeds like ethane and propane are cracked, dilution steam can be added via direct humidification in towers known as feed saturators. This design reduces the load on the dilution steam system and/or medium pressure (MP) steam level. 

Example 20 Estimate the Density of Saturated Liquid Propane... 

Liquefied Petroleum Gas The term liquefied petroleum gas (LPG) is applied to certain specific hydrocarbons which can be liquefied under moderate pressure at normal temperatures but are gaseous under normal atmospheric conditions. The chief constituents of LPG are propane, propylene, butane, butylene, and isobutane. LPG produced in the separation of heavier hydrocarbons from natural gas is mainly of the paraffinic (saturated) series. LPG derived from oil-refinery gas may contain varying low amounts of olefinic (unsaturated) hydrocamons. 

Compounds containing only carbon and hydrogen are termed paraffins or alkanes. The general formula for these compounds is C H2n+2 where n is an integer. When only single bonds are present between carbon atoms they are classified as saturated . Examples include, etliane, propane, and butane the last two are common fuel gases ... 

Saturated — the condition of an organic compound in which each constituent carbon is covalently linked to four different atoms. This is generally a stable configuration (e.g., CHjCHjCHj - propane). 

Because some hydrocracking occurs, Powerforming also produces saturated C to Q light hydrocarbons. The methane and ethane formed normally are consumed as refinery fuel. Propane and butane products are frequently marketed as LPG. The relative quantities of each of these products vary considerably with feed quality, operating conditions and octane severity. 

As mentioned earlier, the detonation velocity depends on the composition of the gas mixture for propane and other saturated hydrocarbons. 

The speciflc work done by the fluid in expansion can be read from Figures 6.30 or 6.31 if its temperature is unknown. Saturated propane at a pressure of 1.9 MPa (19 bar) has a temperature of 328 K, almost the superheat-limit temperature. Note that it is assumed that temperature is uniform, which is not necessarily the case. From Figure 6.30, the expansion work per unit mass for saturated liquid propane is... 

The mass of released liquid propane is 11,958 kg, as was calculated in Section 9.1.6. This gives, for the energy of the explosion for the saturated liquid ... 

The specific work done by a fluid in expansion is read from Figure 6.31 saturated liquid butane 21 MJ/m saturated butane vapor 2.5 MJ/m saturated liquid propane 30 MJ/m saturated propane vapor 8 MJ/m ... 

It is not necessary that the intermediate be separated from the reaction medium in the preparation of the end product. Instead, the reaction mixture, after cooling, is treated with 200 ml of water acidified with 42 ml 10% hydrochloric acid solution, and filtered. To the clear, light yellow filtrate is added dropwise a solution of 9.B g (0.07 mol) 5-nltro-2-furaldehyde in 100 ml ethyl alcohol. An orange solution of the hydrochloride results. The free base is precipitated asyellow plates by making the solution basic with saturated sodium carbonate solution. 14 g of the compound is filtered off by suction, washed with alcohol, and dried. The yield, MP 204°C to 205°C (dec.), is 53% of theoretical based on 3-(N-morpholinyl)-1,2-epoxy-propane. Recrystallization from 95% alcohol (75% recovery) raises the melting point to 206°C (dec.). 

The organic fractions are combined and washed successively with N,N-dimethyl-1,3-propane-diamine, dilute hydrochloric acid, saturated sodium bicarbonate solution and saturated sodium chloride solution. The organic fraction is dried over anhydrous magnesium sulfate. The solvent is then evaporated off. Upon trituration of the residue with methanol, a solid crystallizes, 5-(p-toluovl)-1 -methvlpvrrole-2-acetonitrile, which is removed by filtration and purified by recrystallization from benzene. 

Propane (C.Hg) is one of the saturated open-chain hydrocarbons that form the paraffin or alkane series... 

Alkanes are saturated hydrocarbons having the general formula CnH2n+2- The simplest alkane, methane (CH4), is the principal constituent of natural gas. Methane, ethane, propane, and butane are gaseous hydrocarbons at ambient temperatures and atmospheric pressure. They are usually found associated with crude oils in a dissolved state. 

When crude oil is refined, some of the processes yield additional gaseous products. The C3 and C4 constituents differ from those released from crude oil or from NGLs, which are saturated hydrocarbons. Refinery gases are high in unsaturates, e.g. propane (propylene) and butane (butylenes). These unsaturated hydrocarbons are a valuable source of chemical process intermediates and enjoy a large market alongside naphtha. 

Fig. 8. Partial molar volumes in the saturated liquid phase of the propane-methane system at IOO°F. (O) (0) Data of B. H. Sage and W. N. Lacey, Some Properties of the Lighter Hydrocarbons, Hydrogen Sulfide, and Carbon Dioxide. American Petroleum...

On the other hand, the formation of ethylene was ascribed mainly to the unimolecular decomposition of a neutral excited propane molecule. These interpretations were later confirmed (4) by examining the effect of an applied electrical field on the neutral products in the radiolysis of propane. The yields of those products which were originally ascribed to ion-molecule reactions remained unchanged when the field strength was increased in the saturation current region while the yields of hydrocarbon products, which were ascribed to the decomposition of neutral excited propane molecules, increased several fold because of increased excitation by electron impact. In various recent radiolysis 14,17,18,34) and photoionization studies 26) of hydrocarbons, the origins of products from ion-molecule reactions or neutral excited molecule decompositions have been determined using the applied field technique. However, because of recent advances in vacuum ultraviolet photolysis and ion-molecule reaction kinetics, the technique used in the above studies has become somewhat superfluous. 

Aquilante and Volpi indicate (2) that propanium ions formed by proton transfer from H3 + are not collisionally stabilized at propane pressures as great as 0.3 mm. and that they decompose by elimination of hydrogen or a smaller saturated hydrocarbon to form an alkyl carbonium ion. Others (16, 19) have proposed one or the other of these fates for unstabilized propanium ions. Our observations can be rationalized within this framework by the following mechanisms ... 

The double bonds were reduced to the give the saturated compounds, so the doublebond configuration was not an immediate issue. It appears, however, that the -double bonds are formed. The debenzylated derivatives of propan-1,2,3-triol occur as lipid components in various prokaryotes (archaebacteria) that grow under extreme thermal conditions. 

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