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Naphtha hydrocracking

Properly speaking, steam cracking is not a refining process. A key petrochemical process, it has the purpose of producing ethylene, propylene, butadiene, butenes and aromatics (BTX) mainly from light fractions of crude oil (LPG, naphthas), but also from heavy fractions hydrotreated or not (paraffinic vacuum distillates, residue from hydrocracking HOC). [Pg.382]

Solvents. Petroleum naphtha is a generic term appHed to refined, pardy refined, or unrefined petroleum products. Naphthas are prepared by any of several methods, including fractionation of distillates or even cmde petroleum, solvent extraction, hydrocracking of distillates, polymerization of unsaturated (olefinic) compounds, and alkylation processes. Naphtha can also be a combination of product streams from more than one of these processes. [Pg.210]

Catalytic Reforming. Worldwide, approximately 30% of commercial benzene is produced by catalytic reforming, a process ia which aromatic molecules are produced from the dehydrogenation of cycloparaffins, dehydroisomerization of alkyl cyclopentanes, and the cycHzation and subsequent dehydrogenation of paraffins (36). The feed to the catalytic reformer may be a straight-mn, hydrocracked, or thermally cracked naphtha fraction ia the... [Pg.40]

In addition to straight run naphthas, 70—190°C cuts obtained by distillation from streams produced by cracking high boiling petroleum fractions can also be used as feed to reformers. Naphthas produced by hydrocracking are particularly suitable. [Pg.308]

Naphtha is also obtained from other refinery processing units such as catalytic cracking, hydrocracking, and coking units. The composition of naphtha, which varies appreciably, depends mainly on the cmde type and whether it is obtained from atmospheric distillation or other processing units. [Pg.43]

Naphthas obtained from cracking units generally contain variable amounts of olefins, higher ratios of aromatics, and branched paraffins. Due to presence of unsaturated compounds, they are less stable than straight-mn naphthas. On the other hand, the absence of olefins increases the stability of naphthas produced by hydrocracking units. In refining operations, however, it is customary to blend one type of naphtha with another to obtain a required product or feedstock. [Pg.43]

Heavy naphtha from atmospheric distillation units or hydrocracking... [Pg.43]

Kerosine, a distillate fraction heavier than naphtha, is normally a product from distilling crude oils under atmospheric pressures. It may also he obtained as a product from thermal and catalytic cracking or hydrocracking units. Kerosines from cracking units are usually less stable than those produced from atmospheric distillation and hydrocracking units due to presence of variable amounts of olefinic constituents. [Pg.45]

Catalytic conversion processes include naphtha catalytic reforming, catalytic cracking, hydrocracking, hydrodealkylation, isomerization, alkylation, and polymerization. In these processes, one or more catalyst is used. A common factor among these processes is that most of the reactions are initiated hy an acid-type catalyst that promotes carhonium ion formation. [Pg.60]

Yields Typical yields for severe Naphtha Feed reforming Hydrotreated Hydrocracked... [Pg.67]

Gasoline, coal solvent extn, hydrocracked naphtha... [Pg.123]

This reaction is endothermic and is favored by low pressure. In practice, however, the process is conducted at a pressure of 1-3 MPa (because of a concurrent hydrocracking reaction) and a temperature of 300-450°C using Pt-based catalysts [7]. The feedstock for the reforming process must be carefully purified from S- and N-compounds (below 1 ppm), which may use up a significant portion of hydrogen produced. The typical composition of the off-gas from the catalytic reforming of naphtha is as follows (vol%) H2—82, CH4—7, C2—5, C3—4, and C4—2 [7]. [Pg.91]

A light diesel fuel was produced by distillate hydrotreating of the straight-run Fe-HTFT material, while the heavier fraction was hydrocracked over a dewaxing catalyst, which produced a heavy diesel (Table 18.10). Some diesel fuel was also produced by C3-C4 olefin oligomerization over solid phosphoric acid by recycling the naphtha thus produced. It has previously been pointed out that solid phosphoric acid is not well suited for distillate production,42 and the hydrogenated... [Pg.347]

Superficially the Oryx GTL refinery design has much in common with the SMDS process, but there are important differences. There is no separate hydrotreater, which limits production of chemicals, such as waxes. The hydrocracker employs the Chevron Isocracking technology, which is based on a sulfided supported base-metal catalyst that was designed for crude oil conversion. The operating conditions of the hydrocracker are also more severe (>350°C, 7 MPa) than those required by the SMDS process (300-350°C, 3-5 MPa). Only intermediate products are produced (Table 18.13),5 with the naphtha slated as cracker feed and the distillate as blending component for diesel fuel. [Pg.357]

LPG Unibon An outdated UOP version of the hydrocracking process for simultaneously hydrogenating and cracking a naphtha petroleum fraction to form C3 and C4 hydrocarbons. In 1992 the technology was offered under the umbrella of Unicracking. [Pg.167]

In the hydrocracking process, this phenomenon is exploited to shift catalyst selectivity from the naphtha to the distillate products. Here the wide separation of sites is exploited to minimize the potential for secondary cracking in initial products and intermediates. This, along with the introduction of escape routes for the primary product tends to preserve the higher molecular weight hydrocarbons, thereby producing more dishllates [49, 61, 62]. [Pg.545]


See other pages where Naphtha hydrocracking is mentioned: [Pg.129]    [Pg.160]    [Pg.157]    [Pg.219]    [Pg.129]    [Pg.160]    [Pg.157]    [Pg.219]    [Pg.410]    [Pg.163]    [Pg.458]    [Pg.206]    [Pg.207]    [Pg.361]    [Pg.410]    [Pg.41]    [Pg.182]    [Pg.222]    [Pg.223]    [Pg.224]    [Pg.94]    [Pg.93]    [Pg.221]    [Pg.985]    [Pg.351]    [Pg.360]    [Pg.348]    [Pg.48]    [Pg.109]    [Pg.58]    [Pg.540]    [Pg.561]    [Pg.41]    [Pg.66]    [Pg.101]    [Pg.150]    [Pg.5]    [Pg.18]   
See also in sourсe #XX -- [ Pg.380 , Pg.400 ]




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