Pubdoc 12 6333 432

Properties of Petroleum and Natural Gas
2nd Stage/Chemical Eng. Dept.

Asst. Professor Dr. Hameed Hussein Alwan
---------------------------------------------------------------------------------------------------------------------
8.3.2 Hydrocracking
Hydrocracking is a high-pressure high-temperature process with catalyst for the
conversion of petroleum feedstocks in the presence of H 2 gas; C–C bonds are cleaved,
in addition to the removal of heteroatomic species. Example is the conversion of light
gases and naphtha to jet fuel.
8.4 Reforming Process
Reforming process is the conversion of hydrocarbons with low octane number into
hydrocarbons having higher octane number; e.g., the conversion of n-paraffin into an
iso-paraffin.
8.4.1 Thermal reforming
Thermal reforming is a process using heat (but no catalyst) to effect molecular
rearrangement of low octane naphtha into gasoline of higher antiknock quality.
Thermal reforming was a natural development from older thermal cracking processes;
cracking converts heavier oils into gasoline, whereas reforming convert (reforms)
gasoline into higher-octane gasoline.
A feedstock such naphtha or a straight-run gasoline is heated to 510°C- 595°C in a
furnace with pressures from 400- 1000 psi. As the heated naphtha leaves the furnace, it
is cooled or quenched by the addition of cold naphtha. The material then enters a
fractional distillation tower where any heavy products are separated. The remainder of
the reformed material leaves the top of the tower to be separated into gases and
reformate. Reformate is gasoline with high octane number (65- 80) due to the cracking
of longer-chain paraffins into higher-octane olefins.
8.4.2 Catalytic Reforming
Catalytic reforming convert low octane gasoline into high octane number (90-95)
reformate (higher antiknock quality) by rearranging the HC molecules of gasoline.
1
---------------------------------------------------------------------------------------------------------------------
Catalytic reforming is conducted in the presence of hydrogen over catalysts, which may
be supported on alumina or silica–alumina.
Catalytic reforming is usually carried out by feeding naphtha (after pretreating
with hydrogen if necessary) and hydrogen mixture to a furnace, where the mixture is
heated to the desired temperature, 450°C- 520°C and then passed through fixed-bed
catalytic reactors at hydrogen pressures of 100-1000 psi.
Figure-5 Catalytic reforming Process

8.5 Isomerization Process
It is a process for the conversion of straight chain paraffin hydrocarbon into branched
chain paraffin hydrocarbon with the same atomic composition. Conversion of straight
chain paraffin HC (e.g., butanes, pentanes and hexanes) to their isomers yields gasoline
components of high octane rating.
In the process of isomerization, pure butane or a mixture of isomeric butanes (Figure-6),
is mixed with hydrogen (to inhibit olefin formation) and passed to the reactor, at 110°C-
170°C and 200 - 300 psi in the presence of AlCl 3 catalyst. The product is cooled, the
hydrogen separated and the cracked gases are then removed in a stabilizer column. The
2
---------------------------------------------------------------------------------------------------------------------
stabilizer bottom product is passed to isobutanization column where the normal butane
is separated from the isobutane and recycled.
Figure-6 A butane isomerization unit.

8.6 Alkylation Process
Alkylation is the combination of a branched chain HC (e.g.,isobutane) with an olefin
(e.g., ethylene, propylene, butylene) to form higher isoparaffins. So the process
transforms low molecular weight isoparaffin and alkenes molecules into larger
isoparaffins with a high octane number. Since olefins are reactive (unstable) and are
responsible for exhaust pollutants, their conversion to high octane isoparaffins is
desirable. In refinery practice, only isobutane is alkylated by reaction with normal
butene and isooctane is the product.
The process occurs in presence of a strong acting acid as catalyst. The acid can be
either sulfuric acid or hydrofluoric acid (HF). The product isooctane is a
3
---------------------------------------------------------------------------------------------------------------------
premium gasoline blending stock because it has exceptional antiknock properties and is
clean burning. Conditions of catalytic alkylation; olefins (propylene, butylene) are
combined with isobutane in the presence of an acid catalyst (sulfuric acid or
hydrofluoric acid) at low temperatures and pressures (18°C- 40°C) and 14.8- 150 psi
(Figure-8). Alkylate is composed of a mixture of isoparaffins which have octane
numbers that vary with the olefins from which they were made. All alkylates, however,
have high octane numbers (> 87) which makes them particularly valuable.
Figure-8 An alkylation unit (sulfuric acid catalyst).

8.7 Polymerization Process
Polymerization is the process by which two olefin gases are combined and converted to
higher molecular weight paraffin liquid products which may be suitable for gasoline
(polymer gasoline) or other liquid fuels. Polymer gasoline is the product of
polymerization of gaseous hydrocarbons to hydrocarbons boiling in the gasoline range.
The feedstock usually consists of propylene and butylenes from cracking processes or
may even be selective olefins for dimer, trimer, or tetramer production.
4
---------------------------------------------------------------------------------------------------------------------
Olefins can be conveniently polymerized by means of an acid catalyst (Figure-9). Thus,
the treated, olefin-rich feed stream is contacted with any acid catalyst such as sulfuric
acid, copper pyrophosphate, and phosphoric acid loaded on an inert support at
temperature 150°C- 220°C and pressure 150-1200 psi, depending on feedstock and
product requirement. The process using liquid phosphoric acid catalyst is far more
responsible to attempts to raise production by increasing temperature than the other
processes.
Figure-9 A polymerization unit.

8.8 Solvent Processes
8.81 Deasphalting
Solvent deasphalting processes are a major part of refinery operations and are not often
appreciated for the tasks for which they are used. In the solvent deasphalting processes,
an alkane is injected into the feedstock to disrupt the dispersion of components and
causes the polar constituents to precipitate. Propane is extensively used for deasphalting
and produces a deasphalted oil (DAO) and propane deasphalter asphalt (PDA or PD
tar). Propane has unique solvent properties; at lower temperatures (38°C to 60°C),
paraffins are very soluble in propane and at higher temperatures (about 93°C; 200°F) all
5
---------------------------------------------------------------------------------------------------------------------
hydrocarbons are almost insoluble in propane. A solvent deasphalting unit (Figure-10)
processes the residuum from the vacuum distillation unit and produces deasphalted oil
(DAO), used as feedstock for a fluid catalytic cracking unit, and the asphaltic residue
(deasphalter tar, deasphalter bottoms) which, as a residual fraction, can only be used to
produce asphalt or as a blend stock or visbreaker.
Figure-10 A deasphalting unit.

8.8.2 Dewaxing
Paraff inic crude oils often contain microcrystalline or paraffin waxes. The crude oil
may be treated with a solvent such as methyl-ethyl- ketone (MEK) to remove this wax
before it is processed. This is not a common practice, however and solvent dew axing
processes are designed to remove wax from lubricating oils to give the product good
fluidity characteristics at low temperatures (e.g ., low pour points) rather than from the
whole crude oil. The mechanism of solvent dewaxing involves either the separation of
wax as a soli d that crystallizes from the oil solution at low temperature or the
6
---------------------------------------------------------------------------------------------------------------------
separation of wax as a liquid that is extracted at temperatures above the melting point of
the wax through preferential selectivity of the solvent. However, the former mechanism
is the usual basis for commercial dewaxing processes. The process as now practiced
involves mixing the feedstock with one to four times its volume of the ketone (Figure-
11). The mixture is then heated until the oil is in solution and the solution is chilled at a
slow, controlled rate in double-pipe, scraped-surface exchangers. Cold solvent, such as
filtrate from the filters, passes through the two-inch annular space between the inner
and outer pipes and chills the waxy oil solution flowing through the inner 6-in. pipe.
Figure-11 A solvent dewaxing unit.

Pubdoc 12 6333 432

Uploaded by

Copyright:

Available Formats

Pubdoc 12 6333 432

Uploaded by

Document Information

Original Title

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Pubdoc 12 6333 432

Uploaded by

Copyright:

Available Formats

Properties of Petroleum and Natural Gas

2nd Stage/Chemical Eng. Dept.

Figure-5 Catalytic reforming Process

Figure-6 A butane isomerization unit.

Figure-8 An alkylation unit (sulfuric acid catalyst).

Figure-9 A polymerization unit.

Figure-10 A deasphalting unit.

Figure-11 A solvent dewaxing unit.

You might also like

Pfad - The Proxy pFad of © 2024 Garber Painting. All rights reserved.