US3711568A - Pyrolysis process - Google Patents

Pyrolysis process Download PDF

Info

Publication number
US3711568A
US3711568A US00075150A US3711568DA US3711568A US 3711568 A US3711568 A US 3711568A US 00075150 A US00075150 A US 00075150A US 3711568D A US3711568D A US 3711568DA US 3711568 A US3711568 A US 3711568A
Authority
US
United States
Prior art keywords
pyrolysis
moles
furnace
feed
products
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US00075150A
Inventor
H Cooper
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Application granted granted Critical
Publication of US3711568A publication Critical patent/US3711568A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C4/00Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms
    • C07C4/02Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms by cracking a single hydrocarbon or a mixture of individually defined hydrocarbons or a normally gaseous hydrocarbon fraction
    • C07C4/04Thermal processes
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G9/00Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G9/00Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G9/14Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils in pipes or coils with or without auxiliary means, e.g. digesters, soaking drums, expansion means
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S585/00Chemistry of hydrocarbon compounds
    • Y10S585/919Apparatus considerations
    • Y10S585/921Apparatus considerations using recited apparatus structure
    • Y10S585/924Reactor shape or disposition

Definitions

  • FIG. 2 MULTIPLE FEED POINTS Pyrolysis Zone Separation Facilities FIG.4 28
  • the present invention copes with disadvantages and limitations of the prior art approaches in a novel and facile way.
  • two or more pyrolysis products are recycled to intermediate points on the pyrolysis path in the pyrolysis furnace without addition of feed at those points.
  • Various product streams, each having its own composition, are introduceable at various points along the pyrolysis path in the furnace.
  • One object of this process is to accommodate a wider variety of acceptable feeds than was feasible heretofore while still being able to produce a desired product distribution.
  • Another object of this process is to obtain readily product distributions that would be extremely difficult to obtain by prior-art approaches.
  • Still another object of this process is to minimize formation of undesirable by-products such as coke in the pyrolysis furnace.
  • Still another object of this process is to control more accurately product distribution so that design and/or operation of separating facilities which follow the pyrolysis furnace can be optimized.
  • Still another object of this process is to make a plant embodying the process compatible with computerized control techniques available for optimizing pyrolysis furnace operations.
  • FIG. I is a flow diagram illustrating pyrolysis with conventional recycle.
  • FIG. 2 is a flow diagram illustrating pyrolysis with introduction of a portion of the feed at an intermediate point on the pyrolysis path in the furnace.
  • FIG. 3 is a flow diagram illustrating pyrolysis with recycle of a single product to a single intermediate point along the pyrolysis path in the furnace.
  • FIG. 4 is a flow diagram illustrating pyrolysis with recycle of a plurality of products to a plurality of points along the pyrolysis path in the furnace.
  • feed stream A is introduced to pyrolysis furnace 11 for circulation through coil 12 in non-contact heat exchange relationship with a source of heat.
  • Furnace 11 is provided with inlet 13 and outlet 14 which in turn is connected in series flow relationship with separation facilities 16 wherein the pyrolysis products are separated into streams, for example, 17, 18, 19 and 21.
  • Slip streams 22, 23 and 24 are taken off streams 17, 18 and 19 for recycle via line B to join feed stream A as combined stream C for introduction into the pyrolysis furnace 11 via inlet 13.
  • product stream A generally is divided into major portion C and minor portion D.
  • Major portion C is introduced into furnace 11 via inlet 13 in the usual manner but minor portion D is introduced to the pyrolysis furnace at intermediate point 26. It is also conceivable that D could be the major portion and C the minor portion.
  • portion D at several points along the pyrolysis path has been discussed in the prior art; for example in United States patent 3,579,601 to Kivlin and in United States patent 1,924,848 to Egloff.
  • FIG. 3 A variation of convention recycle and multiple feed points is shown in FIG. 3.
  • a single product stream is recycled to a single intermediate point along the pyrolysis path. Examples of this approach are described in U.S. Pat. No. 3,565,970 to Kelley, particularly at column 4, lines 51 to 55; in U.S. Pat. No. 3,579,438 to Cruse, particularly at column 3, lines 31 to 40 and column 4, lines 27 to 57; and in U.S. Pat. No. 3,470,263 to Kitzen, particularly at column 3, lines 27 to 48 and column 10, lines 35 to 36.
  • U.S. Pat. No. 2,668,791 to Holland also discusses addition of a single material at various points along a pyrolysis path to approach a constant temperature operation.
  • feed stream A is conducted in series through pyrolysis furnace 11 from inlet 13 to outlet 14 and in turn through separation facilities 16 in the usual manner.
  • a slip stream 22 is recycled via line E to intermediate point 26 on the pyrolysis path in the furnace.
  • a plurality of slip streams 22, 23 and 24 can be taken off lines l7, l8 and 19 respectively for recycle to the pyrolysis furnace at intermediate points 26, 27 and 28 respectively.
  • the furnace illustrated herein could be a plurality of furnaces connected in flow series with intermediate points 26 and/or 27 and/or 28 between successive furnaces.
  • the furnaces may be provided with soaking zones wherein heat is not added.
  • the pyrolysis furnace can have a plurality of pyrolysis paths arranged parallel each to the other.
  • an entire product stream could be recycled in lieu of a slip stream and that inert gas or steam may be present in one or more of the streams.
  • Feed is introduced at 950F.
  • Inlet pressure is 150 psia.
  • Tubes are all 60 feet long, 3 inch I.D., 4 inch O.D. Heat transfer rate is 30,000 BTU/hr sq. ft.
  • the total amount of each feed material is constant.
  • the furnace coil length (total) is the same within each example.
  • the steam/hydrocarbon ratio is 0.5 moles/mole.
  • EXAMPLE I Illustrates the effect of recycling propylene to various locations of a pyrolysis furnace having 18 tubes.
  • Pyrolysis furnace feed is 100 moles/hr n-butane and 50 moles/hr of steam.
  • Pyrolysis furnace feed is 16 moles/hr of propylene
  • Feed from Case 11 is split. 80 percent goes to furnace inlet; 20 percent goes to a location where the temperature is approximately 1,565F and the stream contains 14.9 moles/hr of propylene and 14.9 moles/hr of n-butane together with various reaction products (Tube 16).
  • Pyrolysis furnace feed is 100 moles/hr of n-butane and 50 moles/hr of steam.
  • the temperature is approximately 1,420F and the stream contains 50.6 moles/hr of n-butane together with various reaction products a new stream is introduced consisting only of 16 moles/hr of propylene and 8 moles/hr of steam (Tube 16).
  • Feed to pyrolysis furnace is 10 mole/hr of ethane
  • Feed from Case I is split. 50 percent goes to furnace inlet. 25 percent goes to a location at which the temperature is approximately 1,450 and the stream contains 8.3 moles/hr of ethane,
  • Feed to the pyrolysis furnace is 100 moles/hr of nbutane and 50 moles/hr of steam.
  • a temperature is approximately 1,355F and the stream contains'86.9 moles/hr of n-butane together with various products, a
  • Case Product 1 11 111-A lll'B Propylene 32.7 25.7 44.0 32.8 Ethylene 57.5 60.2 52.7 55.5 5 Butylenes 14.2 12.3 14.0 15.3
  • Feed to pyrolysis furnace is 100 mole/hr of n-butane and 50 mole/hr of steam.
  • the stream contains 87 mole/hr of n-butane together with various products a new stream consisting only of 8 mole/hr of hydrogen is added (tube 9).
  • the temperature is approximately 1,395F and the stream contains 66.9 mole/hr of n-butane together with various products a new stream consisting only of 16 mole/hr of propylene and 8 mole/hr of steam is added (tube 13).
  • Feed to pyrolysis furnace is 100 mole/hr of n-butane and 50 mole/hr of steam.
  • a new stream consisting only of 16 mole/hr of propylene and 8 mole/hr of steam is introduced (tube 9).
  • a new stream consisting only of 8 mole/hr of hydrogen is introduced.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

This disclosure teaches a process for pyrolysis of hydrocarbons wherein at least two pyrolysis product are recycled to two different points in the pyrolysis furnace. Three or more pyrolysis products are recycled and introduced into the furnace at a plurality of points on the pyrolysis path.

Description

United States Patent 1191 Cooper Jan. 16, 1973 PYROLYSIS PROCESS [76] Inventor: Herbert W. Cooper, 17 St. Lawrence Place, Jericho, N.Y.
22 Filed: Sept. 24, 1970 21 Appl. No.: 75,150
52 US. Cl ..260/683 R, 208/130, 208/132 511 1111. C1. ..C07c 3/30, 010g 9/36, ClOg 9/14 [58] Field of Search ..260/683; 208/130, 132
[56] References Cited UNITED STATES PATENTS Holland ..208/13O 2,668,791 2/1954 3,579,601 5/1971 Kivlen 3260/6811 3,470,263
9/1969 Kitzen ..260/683 Pyrolysis Zone 3,579,438 5/1971 Cruse ..208/1 32 1,924,848 8/1933 Egloff 2,972,647 2/1961 Fischer at al. ..260/683 3,565,970 2/1971 Kelley ..260/683 Primary ExaminerPaul M. Coughlan, Jr. AsQsistant-Emfniner-C. E. Spresser Attorney-Charles E. Baxley, Frank M. Nolan and Thomas E. Tate 57 ABSTRACT This disclosure teaches a process for pyrolysis of hydrocarbons wherein at least two pyrolysis product are recycled to two different points in the pyrolysis furnace. Three or more pyrolysis products are recycled and introduced into the furnace at a plurality of points on the pyrolysis path.
2 Claims, 4 Drawing Figures Separation Facilities RECYCLE OFA PLURALITY OF PRODUCTS TO INTERMEDIATE POINTS INPYROLYSIS PATH PAIENTEDJAIIIB I973 3,711,568
Separation Facilities 23 24 F I G. I CONVENTIONAL RECYCLE Pyrolysis Zone Separation Facilities 26 FIG. 2 MULTIPLE FEED POINTS Pyrolysis Zone Separation Facilities FIG.4 28
RECYCLE OFA PLURALITY OF PRODUCTS TO INTERMEDIATE POINTS IN PYROLYSIS PATH I Pyrolysis Zone II I6 2 I3 I.-\VENTOR.
I? HERBERT w. COOPER Separation Facilities H6 3 RECYCLE OF ONE PRODUCT TO AN INTERMEDIATE POINT Ammey PYROLYSIS PROCESS BACKGROUND OF THE INVENTION There are two well-known approaches to control of product distributions obtained from pyrolysis furnaces. These approaches form the background of the present disclosure. One of these prior-art approaches contemplates recycling pyrolysis products to the input of the pyrolysis furnace. A second prior-art process contemplates introduction of feed at various points along the pyrolysis path in the furnace. However neither of these prior-art approaches have been able to accommodate a particularly wide variety of feeds while producing a desired product distribution, nor have either of these prior-art approaches been able to control product distribution as accurately as the present invention.
SUMMARY The present invention copes with disadvantages and limitations of the prior art approaches in a novel and facile way. According to this invention two or more pyrolysis products are recycled to intermediate points on the pyrolysis path in the pyrolysis furnace without addition of feed at those points. Various product streams, each having its own composition, are introduceable at various points along the pyrolysis path in the furnace.
One object of this process is to accommodate a wider variety of acceptable feeds than was feasible heretofore while still being able to produce a desired product distribution.
Another object of this process is to obtain readily product distributions that would be extremely difficult to obtain by prior-art approaches.
Still another object of this process is to minimize formation of undesirable by-products such as coke in the pyrolysis furnace.
Still another object of this process is to control more accurately product distribution so that design and/or operation of separating facilities which follow the pyrolysis furnace can be optimized.
Still another object of this process is to make a plant embodying the process compatible with computerized control techniques available for optimizing pyrolysis furnace operations.
BRIEF DESCRIPTION OF DRAWING The foregoing and other features will become apparent from the following detailed description of a preferred embodiment read in conjunction with the enclosed drawing wherein:
FIG. I is a flow diagram illustrating pyrolysis with conventional recycle.
FIG. 2 is a flow diagram illustrating pyrolysis with introduction of a portion of the feed at an intermediate point on the pyrolysis path in the furnace.
FIG. 3 is a flow diagram illustrating pyrolysis with recycle of a single product to a single intermediate point along the pyrolysis path in the furnace.
FIG. 4 is a flow diagram illustrating pyrolysis with recycle of a plurality of products to a plurality of points along the pyrolysis path in the furnace.
DESCRIPTION OF PREFERRED EMBODIMENT As seen in FIG. 1, according to a conventional recycle approach, feed stream A is introduced to pyrolysis furnace 11 for circulation through coil 12 in non-contact heat exchange relationship with a source of heat. Furnace 11 is provided with inlet 13 and outlet 14 which in turn is connected in series flow relationship with separation facilities 16 wherein the pyrolysis products are separated into streams, for example, 17, 18, 19 and 21. Slip streams 22, 23 and 24 are taken off streams 17, 18 and 19 for recycle via line B to join feed stream A as combined stream C for introduction into the pyrolysis furnace 11 via inlet 13. This approach is discussed in U.S. Pat. No. 2,972,647 to Fisher et al.
The pri r-art approach shown in FIG. 2 is comparable to that shown in FIG. 1 except that whether or not recycle is employed, product stream A generally is divided into major portion C and minor portion D. Major portion C is introduced into furnace 11 via inlet 13 in the usual manner but minor portion D is introduced to the pyrolysis furnace at intermediate point 26. It is also conceivable that D could be the major portion and C the minor portion. Introduction of portion D at several points along the pyrolysis path has been discussed in the prior art; for example in United States patent 3,579,601 to Kivlin and in United States patent 1,924,848 to Egloff.
A variation of convention recycle and multiple feed points is shown in FIG. 3. A single product stream is recycled to a single intermediate point along the pyrolysis path. Examples of this approach are described in U.S. Pat. No. 3,565,970 to Kelley, particularly at column 4, lines 51 to 55; in U.S. Pat. No. 3,579,438 to Cruse, particularly at column 3, lines 31 to 40 and column 4, lines 27 to 57; and in U.S. Pat. No. 3,470,263 to Kitzen, particularly at column 3, lines 27 to 48 and column 10, lines 35 to 36. U.S. Pat. No. 2,668,791 to Holland also discusses addition of a single material at various points along a pyrolysis path to approach a constant temperature operation.
According to the present process (as shown in FIG. 4) feed stream A is conducted in series through pyrolysis furnace 11 from inlet 13 to outlet 14 and in turn through separation facilities 16 in the usual manner. A slip stream 22 is recycled via line E to intermediate point 26 on the pyrolysis path in the furnace. A plurality of slip streams 22, 23 and 24 can be taken off lines l7, l8 and 19 respectively for recycle to the pyrolysis furnace at intermediate points 26, 27 and 28 respectively.
It will be understood that this invention is useful with a wide variety of pyrolysis furnaces and with a wide variety of separation facilities. For example, the furnace illustrated herein could be a plurality of furnaces connected in flow series with intermediate points 26 and/or 27 and/or 28 between successive furnaces. The furnaces may be provided with soaking zones wherein heat is not added. Further the pyrolysis furnace can have a plurality of pyrolysis paths arranged parallel each to the other. Also it should be obvious that an entire product stream could be recycled in lieu of a slip stream and that inert gas or steam may be present in one or more of the streams.
EXAMPLES This process will here be exemplified with regard to pyrolysis of normal butane (n-butane) and recycle of propylene, ethane and propylene, as well as propylene and hydrogen. However it should be understood that these examples are merely illustrative and that the inventive concept there advanced has a far wider scope of application than the examples herein contain.
Controlling conditions which prevail throughout the following examples are as follows:
Feed is introduced at 950F.
Inlet pressure is 150 psia.
Tubes are all 60 feet long, 3 inch I.D., 4 inch O.D. Heat transfer rate is 30,000 BTU/hr sq. ft.
The total amount of each feed material is constant.
The furnace coil length (total) is the same within each example.
The steam/hydrocarbon ratio is 0.5 moles/mole.
EXAMPLE I Illustrates the effect of recycling propylene to various locations of a pyrolysis furnace having 18 tubes.
Case I (no recycle per FIG. 1)
Pyrolysis furnace feed is 100 moles/hr n-butane and 50 moles/hr of steam.
Case 11 (conventional recycle per FIG. 1)
Pyrolysis furnace feed is 16 moles/hr of propylene,
100 moles/hr of n-butane, and 58 moles/hr of steam.
Case 111 (multiple feed points per FIG. 2)
Feed from Case 11 is split. 80 percent goes to furnace inlet; 20 percent goes to a location where the temperature is approximately 1,565F and the stream contains 14.9 moles/hr of propylene and 14.9 moles/hr of n-butane together with various reaction products (Tube 16).
Case IV (Invention per FIG. 4)
Pyrolysis furnace feed is 100 moles/hr of n-butane and 50 moles/hr of steam. At a location where the temperature is approximately 1,420F and the stream contains 50.6 moles/hr of n-butane together with various reaction products a new stream is introduced consisting only of 16 moles/hr of propylene and 8 moles/hr of steam (Tube 16).
Major Products (moles per 100 moles of n-butane reacted) Illustrates having 16 tubes.
Case 1 (conventional recycles per FIG. 1)
Feed to pyrolysis furnace is 10 mole/hr of ethane,
16 moles/hr of propylene, 100 moles/hr of n-butane, and 63 moles/hr of steam. Case 11 (multiple feed points per FIG. 2)
the effect of recycling ethane and propylene to various locations of a pyrolysis furnace Feed from Case I is split. 50 percent goes to furnace inlet. 25 percent goes to a location at which the temperature is approximately 1,450 and the stream contains 8.3 moles/hr of ethane,
5 12.6 moles/hr of propylene, and 23.3 moles/hr of n-butane together with various products (Tube 9). The remaining 25 percent goes to a location at which the temperature is approximately 1,455F and the stream contains approxilo mately 11.9 moles/hr of ethane, 18.3 moles/hr of propylene, and 33.3 moles/hr of n-butane (Tube 13). Case 111 A (Invention per FIG. 4) 15 Feed to pyrolysis furnace is 100 moles/hr of n-bu tane and 50 moles/hr of steam. At the location where the temperature is approximately 1,355F
and the stream contains 86.9 moles/hr of n-butane together with various products, a new stream consisting only of 10 moles/hr of ethane and 5 moles/hr of steam is introduced (Tube 9). At a later location where the temperature is approximately 1,385F and the stream contains 17.4 moles/hr of ethane and 69.5 moles/hr of nbutane, together with various products, a new stream is introduced consisting only of 16 moles/hr of propylene and 8 moles/hr of steam (Tube 13).
Case III B (Invention per FIG. 4)
Feed to the pyrolysis furnace is 100 moles/hr of nbutane and 50 moles/hr of steam. At the location where the temperature is approximately 1,355F and the stream contains'86.9 moles/hr of n-butane together with various products, a
new stream consisting only of 16 moles/hr of propylene and 8 moles/hr of steam is introduced (Tube 9). At a later location where the temperature is approximately 1,410F.and the stream contains 24.2 moles/hr of propylene and 63.1
moles/hr of n-butane together with various reaction products a new stream consisting only of 10 moles/hr of ethane and 5 moles/hr of steam is introduced (Tube 13).
Major Products (moles per 100 moles of n-hutane reacted) Case Product 1 11 111-A lll'B Propylene 32.7 25.7 44.0 32.8 Ethylene 57.5 60.2 52.7 55.5 5 Butylenes 14.2 12.3 14.0 15.3
Butadienne 4.4 5.1 3.3 4.1 Hydrogen 23.1 22.5 21.1 22.0 Methane 78.2 90.3 70.6 73.6 Ethane 22.4 16.9 27.4 26.2
5 5 EXAMPLE 111 1,480F, and contains 19.4 moles/hr of n-butane and 1 1.2 moles/hr of propylene, together with various products (tube 9). The remaining 25 percent goes to the location at which the feed is at approximately 1,485F, and contains 26.4 mole/hr of n-butane, and l6.0 mole/hr of propylene, together with various products (tube 13). Case lll A (Invention per FIG. 4)
Feed to pyrolysis furnace is 100 mole/hr of n-butane and 50 mole/hr of steam. At the location where the temperature is approximately 1,355F and the stream contains 87 mole/hr of n-butane together with various products a new stream consisting only of 8 mole/hr of hydrogen is added (tube 9). At a later location where the temperature is approximately 1,395F and the stream contains 66.9 mole/hr of n-butane together with various products a new stream consisting only of 16 mole/hr of propylene and 8 mole/hr of steam is added (tube 13).
Case lIl B (invention per FIG. 4)
Feed to pyrolysis furnace is 100 mole/hr of n-butane and 50 mole/hr of steam. At the location where the temperature is approximately 1,355F and the stream contains 87 mole/hr of n-butane together with various products, a new stream consisting only of 16 mole/hr of propylene and 8 mole/hr of steam is introduced (tube 9). At a later location where the temperature is approximately l,4lOF and the stream contains 23.7 mole/hr of propylene and 67.9 mole/hr of n-butane together with various products a new stream consisting only of 8 mole/hr of hydrogen is introduced.
Major Products (moles per 100 moles of n-butane reacted) Case Product I ll Ill-A Ill-B Propylene 22.2 l4.2 34.0 25.2 Ethylene 55.5 57.9 5 l .2 54.6 Butylenes l6.8 14.2 l6.2 l6.6 Butadienne 4.6 5.4 3.6 4.3 Hydrogen 23.8 2l .0 23.9 24.2 Methane 74.1 91.0 67.1 71.9 Ethane 22.8 l7.4 25.5 23.4
It will be understood by those skilled in pyrolysis that wide deviations can be made from the foregoing examples without departing from the spirit of invention as set forth in the following claims.
1 claim: 1. A process for pyrolysis of a hydrocarbon feed and comprising steps as follows:
providing an elongated pyrolysis zone beginning with an inlet end and terminating with an outlet end and subjected along its length to noncontact heating,
passing the feed through the pyrolysis zone from the inlet end to the outlet end to produce at least a first and a second pyrolysis product each different from the other and from the feed,
separating the first and second pyrolysis products from each other,
recycling a portion of the first pyrolysis products to the pyrolysis zone at a first point between the inlet end and the outlet end, and recycling a portion of the second pyrolysis product to the pyrolysis zone at a second point between the inlet end and the outlet end.
2. The process according to claim 1 wherein:
at least three pyrolysis products are produced each different from the other and from the feed,
and a portion of each of these pyrolysis products are recycled each to a different point along the pyrolysis zone between the inlet end and the outlet end.

Claims (1)

  1. 2. The process according to claim 1 wherein: at least three pyrolysis products are produced each different from the other and from the feed, and a portion of each of these pyrolysis products are recycled each to a different point along the pyrolysis zone between the inlet end and the outlet end.
US00075150A 1970-09-24 1970-09-24 Pyrolysis process Expired - Lifetime US3711568A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US7515070A 1970-09-24 1970-09-24

Publications (1)

Publication Number Publication Date
US3711568A true US3711568A (en) 1973-01-16

Family

ID=22123883

Family Applications (1)

Application Number Title Priority Date Filing Date
US00075150A Expired - Lifetime US3711568A (en) 1970-09-24 1970-09-24 Pyrolysis process

Country Status (1)

Country Link
US (1) US3711568A (en)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4002556A (en) * 1976-04-12 1977-01-11 Continental Oil Company Multiple point injection of hydrogen donor diluent in thermal cracking
US4361478A (en) * 1978-12-14 1982-11-30 Linde Aktiengesellschaft Method of preheating hydrocarbons for thermal cracking
US4414082A (en) * 1978-11-21 1983-11-08 Neary Michael P Process for cracking hydrocarbons
DE3329048A1 (en) * 1982-08-13 1984-02-16 Toyo Engineering Corp., Tokyo METHOD FOR THERMALLY CRACKING HEAVY OIL
US4492624A (en) * 1982-09-30 1985-01-08 Stone & Webster Engineering Corp. Duocracking process for the production of olefins from both heavy and light hydrocarbons
US4548706A (en) * 1983-01-26 1985-10-22 Standard Oil Company (Indiana) Thermal cracking of hydrocarbons
US4615795A (en) * 1984-10-09 1986-10-07 Stone & Webster Engineering Corporation Integrated heavy oil pyrolysis process
US4765883A (en) * 1982-10-20 1988-08-23 Stone & Webster Engineering Corporation Process for the production of aromatics benzene, toluene, xylene (BTX) from heavy hydrocarbons
US4906442A (en) * 1982-09-30 1990-03-06 Stone & Webster Engineering Corporation Process and apparatus for the production of olefins from both heavy and light hydrocarbons
US6337011B1 (en) * 1999-02-19 2002-01-08 Halliburton Energy Services, Inc. Pour point depression unit using mild thermal cracker
CN105622323A (en) * 2014-10-28 2016-06-01 中国石油化工股份有限公司 Steam cracking method
US20220340821A9 (en) * 2019-05-24 2022-10-27 Eastman Chemical Company Thermal Pyoil to a Gas Fed Cracker Furnace

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1924848A (en) * 1926-07-10 1933-08-29 Universal Oil Prod Co Process and apparatus for cracking oil
US2668791A (en) * 1948-10-16 1954-02-09 Gyro Process Co Control of gas production in the vapor phase conversion of liquid hydrocarbons
US2972647A (en) * 1953-06-08 1961-02-21 Hoechst Ag Process for the production of ethylene
US3470263A (en) * 1966-02-24 1969-09-30 Selas Corp Of America Concurrent cracking
US3565970A (en) * 1969-05-26 1971-02-23 Phillips Petroleum Co Hydrocarbon cracking
US3579438A (en) * 1970-04-20 1971-05-18 Monsanto Co Thermal cracking
US3579601A (en) * 1968-06-10 1971-05-18 Exxon Research Engineering Co Pyrolysis of hydrocarbons

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1924848A (en) * 1926-07-10 1933-08-29 Universal Oil Prod Co Process and apparatus for cracking oil
US2668791A (en) * 1948-10-16 1954-02-09 Gyro Process Co Control of gas production in the vapor phase conversion of liquid hydrocarbons
US2972647A (en) * 1953-06-08 1961-02-21 Hoechst Ag Process for the production of ethylene
US3470263A (en) * 1966-02-24 1969-09-30 Selas Corp Of America Concurrent cracking
US3579601A (en) * 1968-06-10 1971-05-18 Exxon Research Engineering Co Pyrolysis of hydrocarbons
US3565970A (en) * 1969-05-26 1971-02-23 Phillips Petroleum Co Hydrocarbon cracking
US3579438A (en) * 1970-04-20 1971-05-18 Monsanto Co Thermal cracking

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4002556A (en) * 1976-04-12 1977-01-11 Continental Oil Company Multiple point injection of hydrogen donor diluent in thermal cracking
US4414082A (en) * 1978-11-21 1983-11-08 Neary Michael P Process for cracking hydrocarbons
US4361478A (en) * 1978-12-14 1982-11-30 Linde Aktiengesellschaft Method of preheating hydrocarbons for thermal cracking
US4740290A (en) * 1982-08-13 1988-04-26 Toyo Engineering Corporation Process for thermal cracking of heavy oil
DE3329048A1 (en) * 1982-08-13 1984-02-16 Toyo Engineering Corp., Tokyo METHOD FOR THERMALLY CRACKING HEAVY OIL
US4906442A (en) * 1982-09-30 1990-03-06 Stone & Webster Engineering Corporation Process and apparatus for the production of olefins from both heavy and light hydrocarbons
US4492624A (en) * 1982-09-30 1985-01-08 Stone & Webster Engineering Corp. Duocracking process for the production of olefins from both heavy and light hydrocarbons
US4765883A (en) * 1982-10-20 1988-08-23 Stone & Webster Engineering Corporation Process for the production of aromatics benzene, toluene, xylene (BTX) from heavy hydrocarbons
US4548706A (en) * 1983-01-26 1985-10-22 Standard Oil Company (Indiana) Thermal cracking of hydrocarbons
US4615795A (en) * 1984-10-09 1986-10-07 Stone & Webster Engineering Corporation Integrated heavy oil pyrolysis process
US6337011B1 (en) * 1999-02-19 2002-01-08 Halliburton Energy Services, Inc. Pour point depression unit using mild thermal cracker
CN105622323A (en) * 2014-10-28 2016-06-01 中国石油化工股份有限公司 Steam cracking method
US20220340821A9 (en) * 2019-05-24 2022-10-27 Eastman Chemical Company Thermal Pyoil to a Gas Fed Cracker Furnace
US12018220B2 (en) * 2019-05-24 2024-06-25 Eastman Chemical Company Thermal pyoil to a gas fed cracker furnace

Similar Documents

Publication Publication Date Title
US3711568A (en) Pyrolysis process
US2377847A (en) Process for converting hydrocarbons
CN105693450B (en) Process and system for producing olefins
US3487121A (en) Hydrocarbon process
US2315107A (en) Catalytic dehydrogenation
US3579601A (en) Pyrolysis of hydrocarbons
Sanfilippo et al. Fluidized bed reactors for paraffins dehydrogenation
US3502737A (en) Ethylbenzene dehydrogenation
CN109336726A (en) A kind of technique of carbon four, light oil and coupling between methanol preparing propylene by catalytic cracking ethylene
GB1384916A (en) Reacation zone control
US2750420A (en) Conversion of hydrocarbons
US3409689A (en) Dehydrogenation process
US3118006A (en) Dehydrogenation of alkylated aromatic hydrocarbons
US2373888A (en) Apparatus for conducting catalytic reactions
US4347396A (en) Process for producing styrene
US3766278A (en) Conversion of hydrocarbons
US3417156A (en) Endothermic catalytic conversion of ethylbenzene to styrene
US2418255A (en) Catalytic dehydrogenation of hydrocarbons
US6875338B2 (en) Process for endothermic conversion of hydrocarbons, its uses, and a unit for carrying out the process
US2461331A (en) Process for dehydrogenation of hydrocarbons in the presence of a gaseous diluent
US3100807A (en) Dehydrogenation of alkylated aromatic hydrocarbons
US2366567A (en) Process for executing catalytic conversions with regenerative contact masses
US2627497A (en) Pebble heater apparatus and method for heat exchange
US2233363A (en) Process for producing paraffinic oils
US3515767A (en) Catalytic conversion process