[0001] This invention relates to oil refining, in particular to producing petroleum coke
by delayed coking.
[0002] There is a delayed coking method, in which the original (primary) mixture is heated
in a furnace and then fed into the lower part of the rectification column where it
mixes with coking products fed from the coking chambers in a vaporous state. When
the liquid primary mixture comes into contact with the steam, some of the least volatile
fractions of the coking products condense, forming the recirculate. Mixing this with
the primary mixture produces a secondary mixture, which is then heated in a furnace
and transferred into one of the alternating coking chambers. To control the recirculation
coefficient, the primary mixture can be fed into the rectification column via several
inlets. When the mixture is fed through the top inlet, the recirculation coefficient
reaches its maximum value. When the primary mixture is fed through the bottom inlet,
i.e. beneath the inlet for the steam of reaction products from the coking chambers,
the recirculation coefficient drops to its lowest value. An alternative method to
control the recirculation coefficient is feeding heavy gasoil to the first sieve plate
in the lower part of the rectification column. [
G. G. Valyavin, B. M. Ezhov and O. M. Salyakhov, "Exploitation of Technological Equipment
and How to Extend Working Periods of Delayed Coking Plants Between Overhauls", Topical
Review, Moscow: TsNIITE Neftekhim, 1979, pp. 30-33.]
[0003] The drawback of this technology is the high recirculation coefficient due to high
energy consumption by heating, cooling and transfer by pumping of a large number of
recirculating fractions, which have very little effect on coking.
[0004] In addition, a high recirculation coefficient reduces the efficiency of the plant
with respect to the original (primary) mixture. The most important drawback is that
the steam of the reaction products, entering the rectification column from the coking
chamber, may carry particles of coke, which, coming inside the reaction chamber together
with the secondary mixture, erode the furnace pipes and coke them up, which makes
frequent overhauls necessary.
[0005] The closest to the proposed invention is the method of producing petroleum coke with
delayed coking which includes heating the original mixture to 300-350°C, separating
the light fractions and heavy residue with a fractionator, using contact facilitating
devices, fractioning the light fractions in a rectification column together with distillate
coking products, feeding the bottoms formed in the rectification column as the recirculate
into the evaporator to mix it with the heavy residue and form the secondary mixture,
coking this mixture, preheated, in the evaporator, producing coke in the coking chambers
and distillate products, which are directed to the rectification column. Quantity
and quality of the bottoms involved in the mixture as a recirculate, are controlled
by feeding a dosed quantity of cooling gasoil to the mass exchangers in the lower
part of the rectification column (Russian Federation Patent No.
2209826, C10B 55/00, published 10 August 2003).
The drawback of this method is the low distillate output, considering that producing
distillates is the main goal of delayed coking because they are used in engine fuels.
[0006] Moreover, this method predetermines the need for frequent overhauls of a delayed
coking plant because using the bottoms from the rectification column, which contain
coke particles carried by distillate coking products from the coking chambers, would
cause erosion and coking up of the furnace pipes of reaction-heating furnaces.
[0007] The proposed invention aims at boosting up the output of distillates and to reduce
the frequency of overhauls at the same time.
[0008] To achieve these goals, the proposed delayed coking method includes heating the primary
mixture at 250-430 °C, feeding the preheated mixture into the evaporator to mix it
with the recirculate and form a secondary mixture, heating the secondary mixture at
460-510 °C, then coking it in the coking chamber, fractioning the light fractions
in the rectification column, producing a gas, benzene, light gasoil and heavy gasoil
and bottoms. Prior to sending the heated mixture into the coking chamber, the secondary
mixture is mixed with bottoms, the quantity and quality of the latter and of heavy
coking gasoil being controlled by controlling temperature on the first plate in the
lower part of the rectification column by using heavy coking gasoil as the reflux
and heavy coking gasoil as the recirculate.
[0009] Involving bottoms from the rectification column in the coking process by supplying
it directly into the coking chamber and also admitting heavy gasoil into the evaporator
as the recirculate will boost up the output of distillates (benzene and light gasoil),
used in engine oils. Using coking heavy gasoil as the recirculate with no carbon particles,
will slow down the coking up of the reaction furnace and reduce erosion of the spiral
tubes and pumps of the reaction furnace, which will reduce the frequency of overhauls
of the delayed coking plant.
[0010] The option of controlling the quantity and quality of heavy gasoil and bottoms provides
an opportunity to optimise the material balance of the plant on distillates output.
[0011] The diagram shows the layout and main parts of the plant for implementation of the
proposed delayed coking technology.
[0012] The plant includes the heat-exchanger 1, the heating/reaction furnace 2, the evaporator
3 with mass exchangers, the rectification column 4, the heating/reaction furnace 5,
and the coking chambers 6.
[0013] The proposed technology works as follows. The original mixture is heated at 230-270
°C in the heat exchanger 1, using the heat of the outgoing streams of products, heated
again, at 350-430 °C, in the furnace 2, and then fed into the lower part of the evaporator
3, equipped with mass exchangers. A strictly controlled quantity of heavy coking gasoil,
used as the recirculate, is delivered from the rectification column 4 onto the first
plate in the upper section of the evaporator. Its amount varies from 2% to 100% or
more on the original mixture, which is known from the level of the equipment used.
The secondary mixture, consisting of the primary mixture and the recirculate, is introduced
at the bottom of the evaporator 3. It is heated at 460-510 °C in the heating furnace
5, and then delivered into one of the alternatively working coking chambers 6 to produce
coke. The coking distillate products formed are passed on from the coking chambers
6 to the lower part of the rectification column 4 for fractioning, via a dome pipe.
Carbon dioxide and benzene are removed from the top part of the rectification column
4.
[0014] Bottoms are removed from the lower part of the rectification column 4. Then they
are transferred either into the coking chambers 6, pre-mixed with the secondary mixture
heated in furnace 5, or brought out as a final product.
[0015] Light and heavy coking gasoil are discharged as side withdraws. The main part of
the heavy gasoil is removed as a final product, while the rest passes into the dome
pipes to serve as a coolant to cool down coking products, to prevent the coking up
of the dome pipe lines and to cool down the bottoms at the bottom of the rectification
column 4. Bottoms, hot or cooled, are passed from the accumulator of the rectification
column 4 to the first plate in the lower part of the rectification column as the reflux
to keep the temperature right in the lower section of the column 4 and on the plate
as the means of controlling the quality of heavy coking gasoil and bottoms.
[0016] Quality and quantity of heavy gasoil and bottoms works as follows.
[0017] When increasing the output of heavy gasoil and increasing its fraction weight with
respect to the end boiling point, the reflux rate onto the first plate in the lower
part of the column 4 is reduced, so that the temperature on the plate goes up. The
output of bottoms removed from the lower section of column 4 goes down simultaneously,
and its fraction weight increases (due to the decreased content of volatile fractions).
[0018] Vice versa, when decreasing the output of heavy gasoil and making its fractional
composition lighter with respect to its end boiling temperature is required, the reflux
rate on the first plate of the rectification column 4 lower section is increased,
so that the temperature on the plate decreases. Some volatile fractions condense simultaneously
and become part of bottoms - due to the lower temperature on the plate. The result
is a greater output of bottoms and a lighter fraction weight.
[0019] The following examples illustrate the proposed method.
EXAMPLE 1 (using the prototype method)
[0020] Tar from West Siberia oil was coked in an industrial delayed coking plant of 1,200,000
tonne/year capacity with respect to the original mixture.
[0021] The original mixture, tar from West Siberia oil (its quality is shown in Table 1)
was heated at 260 °C in heat exchangers, then at 385 °C in a furnace, and then fed
into the lower section of the evaporator. At the same time, recirculate bottoms are
fed from the lower part of the rectification column onto the first plate of the evaporator,
in quantity 10% with respect to the original mixture. The secondary mixture, formed
in the evaporator (a mixture of tar and bottoms) is heated in the furnace at 495 °C,
and then directed to one of the alternately working coking chambers to produce coke.
[0022] Coking distillate products are transferred from the coking chambers to the rectification
column for fractionating to produce a gas, benzene and light and heavy gasoils. The
material balance of coking is shown in Table 1. Coking produced 141,600 tonne/year
of benzene and 272,400 tonne/year of light gasoil, which are used as components in
production of engine fuels. The period between overhauls was 180 days.
EXAMPLE 2 (using the proposed method)
[0023] Like in EXAMPLE 1, tar from West Siberia oil was coked. However, unlike in that example,
heavy coking gasoil was used as the recirculate, obtained as a side withdraw from
the rectification column and fed onto the first plate of the evaporator to the tune
of 10% on the original mixture. Bottoms, 5% in quantity and at 380 °C, was received
from the bottom of the rectification column and mixed with the secondary mixture heated
in the furnace at 500 °C, and directed to the coking chamber. To ensure that the quantity
of bottoms removed from the lower part of the rectification column was 5%, the temperature
on the first plate in the lower part of the rectification column was maintained at
380 °C by feeding cooled heavy gasoil onto it.
[0024] The coking process produced 157,299 tonne/year of benzene and 288,000 of light gasoil.
Quantities of light gasoil and bottoms are presented in Table 3. The time between
two overhauls was 340 days.
EXAMPLE 3 (Using the proposed method)
[0025] Like in Example 1, tar from West Siberia oil was coked. In this example, 20% (on
the original mixture) of heavy gasoil was fed into the evaporator for recirculation.
Feeding cooled heavy gasoil onto the first plate in the lower section of the rectification
column for circulation reflux reduced the temperature on the plate to 365 °C. The
output of bottoms increased to 10% on the original mixture. Bottoms, at 365 °C, were
mixed with the secondary mixture and sent into the coking chambers for coking.
[0026] This coking process produced 168,000 tonne/year of benzene and 298,800 tonnes/year
of gasoil. Qualitative characteristics of heavy coking gasoil and bottoms are shown
in Fig. 3. The period between overhaulls was 340 days.
[0027] One can see that using this technology of producing petroleum coke in delayed coking
ensures that, feeding bottoms directly into the coking chambers, eliminates the possibility
of coke particles carried by the distillate from the coking chambers coming into the
reaction/heating furnaces and, consequently, prevents erosion of furnace pipes and
their premature coking up, which lengthens the periods between overhauls.
[0028] Feeding bottoms into the coking together with the secondary mixture, will increase
the output of coking distillates by approximately 50,000 tonne/year.
[0029] Controlling the quantity of heavy gasoil sent from the accumulator of the rectification
column onto the first plate of the rectification column as reflux by the means of
varying temperature on the plate, allows controlling both quality and quantity of
both heavy coking gasoil and bottoms.
[0030] The opportunity to control the quantity and quality of bottoms, provided its qualitative
and quantitative characteristics fit the standards, will produce additional distillate
fractions to be used as raw materials for catalytic cracking or hydrocracking plants.
TABLE 1
Quality of the primary coking mixture (tar from West Siberia Oil) |
Characteristics |
Quantitative values |
1. Density, ρ420 |
0.9880 |
2. Cokeability, mass% |
15.9 |
3. Kinematic viscosity, cSt at |
|
|
|
80 °C |
2,164 |
|
100 °C |
633 |
4. Chemical composition |
|
|
|
Stot, mass% |
2.33 |
|
V, ppm |
140 |
|
Ni, ppm |
23 |
Fractional distillation according to TBP |
Order number |
Fraction, °C |
Density of narrow fractions, ρ420 |
Fraction content, mass % |
1 |
360-380 |
0.9200 |
0.27 |
2 |
380-400 |
0.9243 |
0.27 |
3 |
400-420 |
0.9343 |
0.24 |
4 |
420-440 |
0.9432 |
0.24 |
5 |
440-460 |
0.9514 |
0.54 |
6 |
460-480 |
0.9601 |
1.39 |
7 |
480-500 |
0.9721 |
4.18 |
8 |
>500 |
1.0027 |
92.88 |
|
Total |
|
100.00 |
Table 2
Material Balance of Coking |
Name |
Product output |
Prototype Example 1 |
Proposed method |
Example 2 |
Example 3 |
mass % |
tonne/year |
Mass % |
tonne/year |
mass % |
tonne/year |
Raw mixture |
100.0 |
1200 |
10.0 |
1200 |
100.0 |
1200 |
Products |
|
|
|
|
|
|
1. CO2 |
8.2 |
98.4 |
8.5 |
102 |
8.9 |
106.8 |
2. Benzene (fr. nk-180°C) |
11.8 |
141.6 |
13.1 |
157.2 |
14.0 |
168 |
3. Light gasoil (180-350 °C) |
22.7 |
272.4 |
24.0 |
288 |
24.9 |
298 |
4. Heavy gasoil (fr.>350 °C) |
29.5 |
354 |
26.4 |
316.8 |
23.9 |
286.8 |
5. Coke |
27.8 |
333.6 |
28.0 |
336 |
28.3 |
339.6 |
Total |
100.0 |
1200 |
100.0 |
1200 |
100.0 |
1200 |
Time between overhauls, days |
180 |
340 |
340 |
Recirculate |
Bottoms |
Heavy gasoil |
Heavy gasoil |
Quantity of recirculate, on raw mixture, % |
|
10 |
|
10 |
|
20 |
Quantity of bottoms into coking, % on raw mixture |
|
10 |
|
5 |
|
10 |
Temperature on first plate, lower section of rectification column, °C |
|
380 |
|
380 |
|
365 |
Table 3
Quality of The Rectification Column Heavy Products |
Characteristic |
Prototype |
Proposed method |
Example 1 |
Example 2 |
Example 3 |
Heavy gasoil |
Bottoms |
Heavy gasoil |
Bottoms |
Heavy gasoil |
Bottoms |
Density, ρ420 |
0.9528 |
0.9832 |
0.9438 |
0.9973 |
0.9382 |
0.9789 |
Cokeability, Mass % |
0.85 |
5.0 |
0.57 |
6.3 |
0.32 |
4.1 |
Contents of carbides, mass % |
- |
1.4 |
- |
1.9 |
- |
0.4 |
Fractal composition: fraction output, mass % |
NC- 300 °C |
4.1 |
1.6 |
5.5 |
2.0 |
7.3 |
4.6 |
300-400 °C |
40.7 |
15.1 |
44.7 |
19.0 |
50.4 |
35.1 |
400-500 °C |
53.6 |
64.3 |
49.2 |
55.0 |
42.3 |
50.3 |
Above 500 °C |
1.6 |
19.0 |
0.6 |
24 |
- |
1.0 |