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Cracking processes vapor-phase

Distillation, vaporizing processes, with cracking 61, Vapor phase cracking... [Pg.365]

Mobil s High Temperature Isomerization (MHTI) process, which was introduced in 1981, uses Pt on an acidic ZSM-5 zeoHte catalyst to isomerize the xylenes and hydrodealkylate EB to benzene and ethane (126). This process is particularly suited for unextracted feeds containing Cg aHphatics, because this catalyst is capable of cracking them to light paraffins. Reaction occurs in the vapor phase to produce a PX concentration slightly higher than equiHbrium, ie, 102—104% of equiHbrium. EB conversion is about 40—65%, with xylene losses of about 2%. Reaction conditions ate temperature of 427—460°C, pressure of 1480—1825 kPa, WHSV of 10—12, and a H2/hydtocatbon molar ratio of 1.5—2 1. Compared to the MVPI process, the MHTI process has lower xylene losses and lower formation of heavy aromatics. [Pg.422]

The feedstocks used ia the production of petroleum resias are obtaiaed mainly from the low pressure vapor-phase cracking (steam cracking) and subsequent fractionation of petroleum distillates ranging from light naphthas to gas oil fractions, which typically boil ia the 20—450°C range (16). Obtaiaed from this process are feedstreams composed of atiphatic, aromatic, and cycloatiphatic olefins and diolefins, which are subsequently polymerized to yield resias of various compositioas and physical properties. Typically, feedstocks are divided iato atiphatic, cycloatiphatic, and aromatic streams. Table 2 illustrates the predominant olefinic hydrocarbons obtained from steam cracking processes for petroleum resia synthesis (18). [Pg.352]

Propylene Dimer. The synthesis of isoprene from propjiene (109,110) is a three-step process. The propjiene is dimeri2ed to 2-methyl-1-pentene, which is then isomeri2ed to 2-methyl-2-pentene in the vapor phase over siUca alumina catalyst. The last step is the pyrolysis of 2-methyi-2-pentene in a cracking furnace in the presence of (NH 2 (111,112). Isoprene is recovered from the resulting mixture by conventional distillation. [Pg.468]

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. [Pg.208]

Gyro Also called Gyro-cracking. An early vapor-phase thermal cracking process for refining petroleum. [Pg.120]

TVP [True vapor-phase] A thermal cracking process in which vaporized petroleum oil is contacted with a hotter gas such that the temperature of the gas mixture is approximately 500°C. Used in the 1930s, but supplanted by various catalytic cracking processes. [Pg.276]

Gray clay treating a fixed-bed (q.v.), usually fuller s earth (q.v.), vapor-phase treating process to selectively polymerize unsaturated gum-forming constituents (diolefins) in thermally cracked gasoline. [Pg.435]

Vapor-phase cracking a high-temperature, low-pressure conversion process. [Pg.458]

Cold box and refrigeration system. After the acid gas and water removal, the pyrolysis gas is cooled and condensed to approximately -165°C only hydrogen and some methane remain in the vapor phase. The feed locations are determined via process simulation. Hydrogen and methane are drawn from the lowest temperature stage separator and sent to thermal cracking furnaces as fuel. [Pg.2984]

In the early days of the industry, gasoline was of little value. Cracking was used to produce more kerosene than could be obtained by steam or simple distillation. At first, cracking was done by the decomposition of vapors, later liquid-phase cracking processes would include viscosity breaking and reforming. [Pg.58]


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