US3786110A - Asphaltenes for inhibiting polymerization of pyrolysis products - Google Patents

Asphaltenes for inhibiting polymerization of pyrolysis products Download PDF

Info

Publication number
US3786110A
US3786110A US00254956A US3786110DA US3786110A US 3786110 A US3786110 A US 3786110A US 00254956 A US00254956 A US 00254956A US 3786110D A US3786110D A US 3786110DA US 3786110 A US3786110 A US 3786110A
Authority
US
United States
Prior art keywords
asphaltenes
pyrolysis
hydrocarbons
products
pyrolysis 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
US00254956A
Inventor
T Oleszko
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.)
Marathon Oil Co
Original Assignee
Marathon Oil Co
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 Marathon Oil Co filed Critical Marathon Oil Co
Application granted granted Critical
Publication of US3786110A publication Critical patent/US3786110A/en
Assigned to MARATHON OIL COMPANY, AN OH CORP reassignment MARATHON OIL COMPANY, AN OH CORP ASSIGNS THE ENTIRE INTEREST Assignors: MARATHON PETROLEUM COMPANY
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • 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
    • C10G9/002Cooling of cracked gases
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D51/00Auxiliary pretreatment of gases or vapours to be cleaned
    • B01D51/10Conditioning the gas to be cleaned
    • 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
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/20Use of additives, e.g. for stabilisation
    • 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
    • Y10S585/909Heat considerations
    • Y10S585/911Heat considerations introducing, maintaining, or removing heat by atypical procedure

Definitions

  • the present invention relates generally to hydrocarbon pyrolysis processes, e.g., to produce acetylene, classified in Class 260, subclass 679 of United States Patent Classification system.
  • 2,970,099 forms an asphalt comprising an alkylated asphaltene fraction having a carbon-to-hydrogen atomic ratio of 0.72 0.84.
  • Alkylating agents include particularly alkyl halides, alkenes and alkanes; US. Pat. 3,089,846 forms a well drilling composition by dispersing asphaltene carboxylic acids into a fluid medium consisting of water, oil, and an emulsion of water and oil; US. Pat. 3,146,118 prepares an asphalt by blending a telomer of asphaltenes and ester with an asphalt cutter stock.
  • the telomer is formed by precipitating asphaltenes of an asphalt with a C alkane and heating the asphaltenes With C alkyl ester of an acrylic acid in the presence of an organic peroxide;
  • U.S. Pat. 3,366,702 adds oxy-compound inhibitors to pyrolysis products at a point downstream from the quench;
  • US. Pat. 3,190,934 separates a hydrocarbon mixture consisting essentially of C -C aromatic and aliphatic hydrocarbons into aromatic-rich and aromatic-lean fractions by extracting with bituminous material, e.g., asphaltenes, resins, and asphaltic oils; US. Pat.
  • 3,231,488 hydrorefines a hydrocarbon charge stock containing less than about 0.1% by weight of pentane-insoluble asphaltenes by heating at below about 210 C. an asphaltene mixed with a carbonyl, a beta-diketone complex and a heteropoly acid.
  • the resulting colloidal suspension is then reacted with hydrogen at about 225 C. and above 500 p.s.i.g.; US. Pat. 3,303,151 polymerizes a vinyl com- 3,786,110 Patented Jan. 15, 1974 "ice pound with an asphaltic material containing a transition metal and a reducing agent, i.e., metal hydrides, alkyls, aryls, or sesquihalides; and US. Pat. 3,317,447 prepares asphaltenes by heating a mixture of asphaltenes and polypropylene with 130% by weight of sulfur.
  • the present invention provides the new solution to a previously serious problem without involving the need for purchase of raw materials which are not already available in most refineries.
  • the polymerization inhibitors which can themselves be hydrocarbons, are not deleterious to the use of the pyrolysis products in any application in which such products are normally used.
  • the present invention is useful with any of a wide variety of pyrolysis methods including partial oxidation techniques, the well known regenerative Wulff process taught in e.g., U.S. Pats. 1,996,185; 2,037,056; 2,236,534; 2,236,535; 2,236,555; 2,319,679; and 2,518,688, and any other process which involves the pyrolysis of hydrocarbons or substituted hydrocarbons in high temperature zones to form unsaturates which tend to polymerize in the downstream equipment.
  • the deposits prevented or alleviated by the present invention previously required very heavy amounts of maintenance in equipment downstream from the pyrolysis zone.
  • quench towers previously became nearly filled with deposits which were sufliciently hard that they had to be removed by air-operated jack hammers (such as are used to break up concrete roads or concrete blocks).
  • air-operated jack hammers such as are used to break up concrete roads or concrete blocks.
  • the addition of relatively small amounts of asphalt-containing topped whole crude, according to the present invention reduced the deposits to relatively thin coatings of a buttery consistency which were readily scraped from the tower.
  • the tower had previously required cleaning approximately every four to six weeks, and after the application of the invention, required cleaning only about every 12 months. The plant is no longer shut down for cleaning of the quench tower but operates between normal turnarounds. Cleaning is only incidental to the turnaround and is negligible.
  • the drawing is a schematic representation of a typical Wultf pyrolysis installation showing the point of injection of the asphaltenes according to the present invention.
  • the pyrolysis feedstocks for the present invention can be any of a wide variety of hydrocarbons including any hydrocarbons from C to about C more preferably aliphatic hydrocarbons in the range of from about C to about C and most preferably alkanes either straight or branch chain in the range of from about C to about C These may be substituted hydrocarbons if desired, e.g., by halogens (e.g., fiuoro carbon feedstocks such as trichloromonofiuoroethane, etc.) or by sulfonates, nitrates, substituted aromatics and ethers.
  • halogens e.g., fiuoro carbon feedstocks such as trichloromonofiuoroethane, etc.
  • sulfonates nitrates, substituted aromatics and ethers.
  • Suitable feedstocks include ethylene dichloride, nitroethane, chlorohexane, benzyl nitrate, butane, propane, light and heavy naphthas, refinery off gases, ethyl benzene and methane. It should be understood that treatment with asphaltenes is applicable to all manner of hydrocarbons subjected to pyrolyzing because even methane, when pyrolyzed, yields ethylene and a variety of heavier hydrocarbons which can cause deposits of the type alleviated or eliminated by application of the present invention.
  • Asphalts are preferably residues from a distillation which removes materials lighter than about 650 C. Suitable sources of asphalts are crude oil, tar sands, and asphalt lakes. In general, the asphalts may be any of the heavy ends derived from crude oils, especially preferably asphaltic crudes.
  • Useful sources of asphalts are whole crudes, particularly asphaltic crudes, crude residues which contain asphalts, topped crudes, reduced crudes (crude tower bottoms), and especially preferred, vacuum tower bottoms. Gas oils and other lighter materials are generally undesirable for this purpose.
  • asphalts Preferably from about 0.10 to about 25, more preferably from 0.5 to 15, and most preferably from 2.0 to about 10 percent by volume of asphalts will be added to the liquid pyrolysis products.
  • the quantity of asphalt to be added depends upon the nature and quantity of free or unstable, easily polymerizable hydrocarbons present.
  • Pyrolysis products The cracked gases produced in the pyrolysis of the above hydrocarbon and other feeds will generally be benzene, xylenes, toluene, and olefins, as well as ethylene and acetylene.
  • the bottoms from the pyrolysis process are generally heavy aromatics such as naphthalenes and alkyl-substituted naphthalenes.
  • substituted products are utilized as feed, the products will themselves generally be substituted, e.g., with nitrates, sulfates, halo groups, etc.
  • Pyrolysis process While the invention is particularly A useful with the Wulff pyrolysis process in which regenerative furnaces rapidly heat the feed and in which quench oils rapidly cool the pyrolysis products, the invention can also be used with other conventional pyrolysis techniques, e.g., steam crackers for ethylene production or production of other olefins, partial oxidation processes for production of unsaturates, thermal dehalogenation, etc.
  • other conventional pyrolysis techniques e.g., steam crackers for ethylene production or production of other olefins, partial oxidation processes for production of unsaturates, thermal dehalogenation, etc.
  • EXAMPLE Hydrocarbons are fed to pyrolysis furnace 10 which is, in this example, a Wultf regenerative pyrolysis furnace which is alternately heated by combustion of fuel gas (not shown) and then used to crack hydrocarbons by contact with the hot furnace refractories.
  • the hydrocarbons fed are naphthas produced from Malawin crude together with minor hydrocarbon fraction streams obtained from other points in the refinery.
  • the pyrolysis furnace operates at approximately 1200 C. and the products are about 25 tons per hour of hydrogen, ethane, methane, ethylene, acetylene, and minor amounts of carbon and other products.
  • the hot pyrolysis products are fed to a lower stage 11 of quench tower 12 where they contact quench oil 13 sprayed from nozzles 14 fed by a pump 15 via cooler 16.
  • the quench oil is collected at the bottom outlet 17 of the quench tower 12 and is recycled through cooler 16 back into the spray heads 14.
  • About eight tons per hour of a stream of octane and heavier hydrocarbons is withdrawn for further purification or for burning.
  • About 18 tons of hydrogen and Cq-lOWCI' hydrocarbons is withdrawn from the quench tower as overheads and is sent for further purification, particularly to recover ethane and acetylene.
  • one ton per hour of an asphaltene-containing stream (in this case atmospheric tower bottoms obtained from the distillation of shamen crude in a conventional tower operating at ap proximately 2.5 absolute), is fed to the stream of quench oil being circulated to the nozzles 14.
  • This feed is continued over a period of months of operation and it is found that the deposits on the downstream equipment are greatly reduced in quantity and that their consistency is similar to that of warm butter or a soft grease.
  • the deposits are readily removed by low pressure water stream or hand scraping performed during routine maintenance at 12 month intervals, the normal turnaround interval.
  • hydrocarbons or substituted hydrocarbons comprise whole or topped crude oil.
  • hydrocarbons are selected from the group consisting of refinery off gases, hydrogen, methane, ethane, ethylene, propane, propylene, C and C light and heavy straight-run naphthas, and naphtha from thermal cracking processes and mixtures thereof.
  • asphaltcontaining hydrocarbons are selected from the group consisting of crude oil, reduced crude, vacuum-reduced crude and mixtures thereof.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Water Supply & Treatment (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

UNDESIRED RESIDUES FROM POLYMERS OBTAINED DURING PYROLYSIS OF PETROLLEUM FRACTIONS ARE REDUCED BY INCORPORATING UNOXIDIZED OR PARTIALLY OXIDIZED ASPHALTENES INTO THE PYROLYSIS PRODUCT STREAMS. THE ASPHALTENES PROVIDE SITE FOR POLYMER MOLECULES TO ATTACH THEMSELVES; ALSO

ASPHALTENES ARE CAPABLE OF REACTING WITH THE HIGHLY REACTIVE POLYOLEFINS TO FORM LOW MOLECULAR WEIGHT POLYMERS-SUCH PREVENT THE FORMING OF HIGH MOLECULAR WEIGHT POLYMERS.

Description

T. J. OLESZKO 3,786,110
ASPHALFENES FOR TNHIBITING POLYMEBIZATTUN OF PYROLYSIS PRODUCTS Jan. 15, 1974 Filed May 19, 1972 ZOFEOIEDA OP IN N P United States Patent US. Cl. 260-679 R 9 Claims ABSTRACT OF THE DISCLOSURE Undesired residues from polymers obtained during pyrolysis of petroleum fractions are reduced by incorporating unoxidized or partially oxidized asphaltenes into the pyrolysis product streams. The asphaltenes provide sites for polymer molecules to attach themselves; also asphaltenes are capable of reacting with the highly reactive polyolefins to form low molecular weight polymers-such prevent the forming of high molecular weight polymers.
CROSS REFERENCES TO RELATED APPLICATIONS No related US. patent applications are known to the inventor.
BACKGROUND OF THE INVENTION Field of the Invention The present invention relates generally to hydrocarbon pyrolysis processes, e.g., to produce acetylene, classified in Class 260, subclass 679 of United States Patent Classification system.
Description of the Prior Art A search in the U .8. Patent Office disclosed the following prior art: US. Pat. 2,864,498 alters the ratio of octane-soluble, magnesia-adsorbable petroleum resins to octane-precipitable, benzene-soluble asphaltenes in an oil to reduce the tendency of such oil to form stable emulsions with water; US. Pat. 2,967,818 separates an asphaltic bituminous material into a heavy fraction containing asphaltenes and resins substantially free of asphaltene oils and a lighter solvent fraction containing dissolved residual asphaltic bituminous material including oils; US. Pat. 2,970,099 forms an asphalt comprising an alkylated asphaltene fraction having a carbon-to-hydrogen atomic ratio of 0.72 0.84. Alkylating agents include particularly alkyl halides, alkenes and alkanes; US. Pat. 3,089,846 forms a well drilling composition by dispersing asphaltene carboxylic acids into a fluid medium consisting of water, oil, and an emulsion of water and oil; US. Pat. 3,146,118 prepares an asphalt by blending a telomer of asphaltenes and ester with an asphalt cutter stock. The telomer is formed by precipitating asphaltenes of an asphalt with a C alkane and heating the asphaltenes With C alkyl ester of an acrylic acid in the presence of an organic peroxide; U.S. Pat. 3,366,702 adds oxy-compound inhibitors to pyrolysis products at a point downstream from the quench; US. Pat. 3,190,934 separates a hydrocarbon mixture consisting essentially of C -C aromatic and aliphatic hydrocarbons into aromatic-rich and aromatic-lean fractions by extracting with bituminous material, e.g., asphaltenes, resins, and asphaltic oils; US. Pat. 3,231,488 hydrorefines a hydrocarbon charge stock containing less than about 0.1% by weight of pentane-insoluble asphaltenes by heating at below about 210 C. an asphaltene mixed with a carbonyl, a beta-diketone complex and a heteropoly acid. The resulting colloidal suspension is then reacted with hydrogen at about 225 C. and above 500 p.s.i.g.; US. Pat. 3,303,151 polymerizes a vinyl com- 3,786,110 Patented Jan. 15, 1974 "ice pound with an asphaltic material containing a transition metal and a reducing agent, i.e., metal hydrides, alkyls, aryls, or sesquihalides; and US. Pat. 3,317,447 prepares asphaltenes by heating a mixture of asphaltenes and polypropylene with 130% by weight of sulfur.
SUMMARY OF THE INVENTION General Statement of the Invention According to the invention, in a process for the pyrolysis of hydrocarbons or substituted hydrocarbons in a high temperature zone followed by rapid cooling in a quench zone, the serious problem of formation of hard deposits on the interior of apparatus downstream from the quench zone is solved by the simple expedient of adding asphaltenes to the pyrolysis products in or (less preferably) just after the quench zone. It is an important feature of the invention that the asphaltenes which are readily available in most refineries, e.g. those contained in many Whole crudes, may be utilized as the inexpensive polymerization inhibitor for alleviating this problem. Thus the present invention provides the new solution to a previously serious problem without involving the need for purchase of raw materials which are not already available in most refineries. Further, the polymerization inhibitors, which can themselves be hydrocarbons, are not deleterious to the use of the pyrolysis products in any application in which such products are normally used.
Utility of the Invention The present invention is useful with any of a wide variety of pyrolysis methods including partial oxidation techniques, the well known regenerative Wulff process taught in e.g., U.S. Pats. 1,996,185; 2,037,056; 2,236,534; 2,236,535; 2,236,555; 2,319,679; and 2,518,688, and any other process which involves the pyrolysis of hydrocarbons or substituted hydrocarbons in high temperature zones to form unsaturates which tend to polymerize in the downstream equipment.
The deposits prevented or alleviated by the present invention previously required very heavy amounts of maintenance in equipment downstream from the pyrolysis zone. For example, in one major Wullf pyrolysis installation, quench towers previously became nearly filled with deposits which were sufliciently hard that they had to be removed by air-operated jack hammers (such as are used to break up concrete roads or concrete blocks). The addition of relatively small amounts of asphalt-containing topped whole crude, according to the present invention, reduced the deposits to relatively thin coatings of a buttery consistency which were readily scraped from the tower. The tower had previously required cleaning approximately every four to six weeks, and after the application of the invention, required cleaning only about every 12 months. The plant is no longer shut down for cleaning of the quench tower but operates between normal turnarounds. Cleaning is only incidental to the turnaround and is negligible.
BRIEF DESCRIPTION OF THE DRAWING The drawing is a schematic representation of a typical Wultf pyrolysis installation showing the point of injection of the asphaltenes according to the present invention.
DESCRIPTION OF THE PREFERRED EMBODIMENTS Starting materials-Pyrolysis feedstocks: The pyrolysis feedstocks for the present invention can be any of a wide variety of hydrocarbons including any hydrocarbons from C to about C more preferably aliphatic hydrocarbons in the range of from about C to about C and most preferably alkanes either straight or branch chain in the range of from about C to about C These may be substituted hydrocarbons if desired, e.g., by halogens (e.g., fiuoro carbon feedstocks such as trichloromonofiuoroethane, etc.) or by sulfonates, nitrates, substituted aromatics and ethers. Suitable feedstocks include ethylene dichloride, nitroethane, chlorohexane, benzyl nitrate, butane, propane, light and heavy naphthas, refinery off gases, ethyl benzene and methane. It should be understood that treatment with asphaltenes is applicable to all manner of hydrocarbons subjected to pyrolyzing because even methane, when pyrolyzed, yields ethylene and a variety of heavier hydrocarbons which can cause deposits of the type alleviated or eliminated by application of the present invention.
Asphalts: The asphalts for use with the present invention are preferably residues from a distillation which removes materials lighter than about 650 C. Suitable sources of asphalts are crude oil, tar sands, and asphalt lakes. In general, the asphalts may be any of the heavy ends derived from crude oils, especially preferably asphaltic crudes.
Useful sources of asphalts are whole crudes, particularly asphaltic crudes, crude residues which contain asphalts, topped crudes, reduced crudes (crude tower bottoms), and especially preferred, vacuum tower bottoms. Gas oils and other lighter materials are generally undesirable for this purpose.
Preferably from about 0.10 to about 25, more preferably from 0.5 to 15, and most preferably from 2.0 to about 10 percent by volume of asphalts will be added to the liquid pyrolysis products. In a large measure, the quantity of asphalt to be added depends upon the nature and quantity of free or unstable, easily polymerizable hydrocarbons present.
Pyrolysis products: The cracked gases produced in the pyrolysis of the above hydrocarbon and other feeds will generally be benzene, xylenes, toluene, and olefins, as well as ethylene and acetylene. The bottoms from the pyrolysis process are generally heavy aromatics such as naphthalenes and alkyl-substituted naphthalenes. Of course, where substituted products are utilized as feed, the products will themselves generally be substituted, e.g., with nitrates, sulfates, halo groups, etc.
Pyrolysis process: While the invention is particularly A useful with the Wulff pyrolysis process in which regenerative furnaces rapidly heat the feed and in which quench oils rapidly cool the pyrolysis products, the invention can also be used with other conventional pyrolysis techniques, e.g., steam crackers for ethylene production or production of other olefins, partial oxidation processes for production of unsaturates, thermal dehalogenation, etc.
EXAMPLE Hydrocarbons are fed to pyrolysis furnace 10 which is, in this example, a Wultf regenerative pyrolysis furnace which is alternately heated by combustion of fuel gas (not shown) and then used to crack hydrocarbons by contact with the hot furnace refractories. The hydrocarbons fed are naphthas produced from Libyan crude together with minor hydrocarbon fraction streams obtained from other points in the refinery. The pyrolysis furnace operates at approximately 1200 C. and the products are about 25 tons per hour of hydrogen, ethane, methane, ethylene, acetylene, and minor amounts of carbon and other products. The hot pyrolysis products are fed to a lower stage 11 of quench tower 12 where they contact quench oil 13 sprayed from nozzles 14 fed by a pump 15 via cooler 16. The quench oil is collected at the bottom outlet 17 of the quench tower 12 and is recycled through cooler 16 back into the spray heads 14. About eight tons per hour of a stream of octane and heavier hydrocarbons is withdrawn for further purification or for burning. About 18 tons of hydrogen and Cq-lOWCI' hydrocarbons is withdrawn from the quench tower as overheads and is sent for further purification, particularly to recover ethane and acetylene.
The above description of this example is substantially conventional operation of a Wufr" unit. Over a period of time, the downstream purification equipment as well as the upper portions of the quench tower will become caked with polymerized deposits which will be mechanically strong and difficult to remove.
According to the present invention, one ton per hour of an asphaltene-containing stream (in this case atmospheric tower bottoms obtained from the distillation of Libyan crude in a conventional tower operating at ap proximately 2.5 absolute), is fed to the stream of quench oil being circulated to the nozzles 14. This feed is continued over a period of months of operation and it is found that the deposits on the downstream equipment are greatly reduced in quantity and that their consistency is similar to that of warm butter or a soft grease. The deposits are readily removed by low pressure water stream or hand scraping performed during routine maintenance at 12 month intervals, the normal turnaround interval.
MODIFICATIONS OF THE INVENTION A variety of modifications and variations in the invention will be apparent to those skilled in the art upon a reading of the present specification and it should be understood that all such modifications and variations are to be included within the spirit of the claims appended hereto.
What is claimed is:
1. In a process for the manufacture of unsaturated hydrocarbons or unsaturated substituted hydrocarbons by the pyrolysis of hydrocarbons or substituted hydrocarbons by first pyrolyzing at elevated temperature and thereafter quenching the products of said pyrolysis, comprising adding to said pyrolysis products during said quenching stepa quantity of polymerization inhibitor to inhibit the formation of high molecular weight deposits on equipment used in said quenching step and on downstream equipment, the improvement wherein said inhibitor consists essentially of asphalt-containing hydrocarbons boiling above about 650 C.
2. A process according to claim 1 wherein said hydrocarbons or substituted hydrocarbons comprise whole or topped crude oil.
3. A process according to claim 1 wherein said hydrocarbons are selected from the group consisting of refinery off gases, hydrogen, methane, ethane, ethylene, propane, propylene, C and C light and heavy straight-run naphthas, and naphtha from thermal cracking processes and mixtures thereof.
4. A process according to claim 1 wherein said asphaltcontaining hydrocarbons are selected from the group consisting of crude oil, reduced crude, vacuum-reduced crude and mixtures thereof.
5. In a process for the manufacture of unsaturated hydrocarbons or unsaturated substituted hydrocarbons for the pyrolysis of hydrocarbons or substituted hydrocarbons by first pyrolyzing at elevated temperature and thereafter cooling the products of said pyrolysis, comprising adding to said pyrolysis products during said cooling step a quantity of a polymerization inhibitor to reduce the formation of high molecular weight deposits on equipment 9. A process according to claim 8 wherein said asphaltcontaining hydrocarbon is vacuum-reduced crude containing minimum quantity of distillable gas oils.
References Cited UNITED STATES PATENTS 3,255,270 6/ 1966 Teltschik 260-679 R 3,392,210 7/1968 Puistonen 260-679 R 3,236,906 2/1966 Otsuka et a1. 208-48 QX 6 2,864,498 12/ 1958 Matthew et a1. 208-15 3,190,934 6/1965 Garwin 260-674 SE DELBERT E. GANTZ, Primary Examiner 5 J. M. NELSON, Assistant Examiner US. Cl. X.R.
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3 786 llO Dated January 15 1974 Inventor(s) Thaddeus J. Oleszko It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
After "2.5" insert Col. 4, line 12:
--atmospheres-.
Signed and sealed I this 17th day of September 1974.
(SEAL) Attest:
MCCQY M. GIBSON JR. C. MARSHALL DANN Atte'sting Officer Commissioner of Patents FORM PC4050 (1069) USCOM Dc 5037 M- e-PM v u s covznumzm PRINYING omcz: I!" 0366-334,
US00254956A 1972-05-19 1972-05-19 Asphaltenes for inhibiting polymerization of pyrolysis products Expired - Lifetime US3786110A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US25495672A 1972-05-19 1972-05-19

Publications (1)

Publication Number Publication Date
US3786110A true US3786110A (en) 1974-01-15

Family

ID=22966231

Family Applications (1)

Application Number Title Priority Date Filing Date
US00254956A Expired - Lifetime US3786110A (en) 1972-05-19 1972-05-19 Asphaltenes for inhibiting polymerization of pyrolysis products

Country Status (3)

Country Link
US (1) US3786110A (en)
BR (1) BR7303612D0 (en)
GB (1) GB1428259A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2416933A1 (en) * 1978-02-10 1979-09-07 Linde Ag PROCESS FOR SEPARATING, IN ITS CONSTITUENTS, OF A MIXTURE OF HYDROCARBONS
US4294800A (en) * 1978-10-30 1981-10-13 Tavlarides Lawrence L Liquid jet recycle reactor
US5019239A (en) * 1989-11-21 1991-05-28 Mobil Oil Corp. Inverted fractionation apparatus and use in a heavy oil catalytic cracking process
US5805336A (en) * 1996-04-05 1998-09-08 Polaroid Corporation Optical lens blank with polarizer aligned between plastic birefringent sheets
FR2834515A1 (en) * 2002-01-10 2003-07-11 Atofina MODIFIED NAPHTHA SPRAYING
US20140102874A1 (en) * 2011-05-26 2014-04-17 Exxonmobil Chemical Patents Inc. Method of Flushing Pyrolysis Reactor

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2416933A1 (en) * 1978-02-10 1979-09-07 Linde Ag PROCESS FOR SEPARATING, IN ITS CONSTITUENTS, OF A MIXTURE OF HYDROCARBONS
US4294800A (en) * 1978-10-30 1981-10-13 Tavlarides Lawrence L Liquid jet recycle reactor
US5019239A (en) * 1989-11-21 1991-05-28 Mobil Oil Corp. Inverted fractionation apparatus and use in a heavy oil catalytic cracking process
US5805336A (en) * 1996-04-05 1998-09-08 Polaroid Corporation Optical lens blank with polarizer aligned between plastic birefringent sheets
FR2834515A1 (en) * 2002-01-10 2003-07-11 Atofina MODIFIED NAPHTHA SPRAYING
WO2003057802A2 (en) * 2002-01-10 2003-07-17 Atofina Steam-cracking of modified naphtha
WO2003057802A3 (en) * 2002-01-10 2004-04-15 Atofina Steam-cracking of modified naphtha
US20060089518A1 (en) * 2002-01-10 2006-04-27 Atofina Steam-cracking of modified naphtha
US7838712B2 (en) 2002-01-10 2010-11-23 Total Petrochemicals Research Feluy Steam-cracking of modified naphtha
US20140102874A1 (en) * 2011-05-26 2014-04-17 Exxonmobil Chemical Patents Inc. Method of Flushing Pyrolysis Reactor
US9963641B2 (en) * 2011-05-26 2018-05-08 Exxonmobil Chemical Patents Inc. Method of flushing pyrolysis reactor

Also Published As

Publication number Publication date
GB1428259A (en) 1976-03-17
BR7303612D0 (en) 1974-07-18

Similar Documents

Publication Publication Date Title
US4239616A (en) Solvent deasphalting
US2940920A (en) Separation of asphalt-type bituminous materials
US3687840A (en) Delayed coking of pyrolysis fuel oils
CN103814112B (en) The delayed coking method of solvent auxiliary
US3382084A (en) Asphalt binder pitch
US20010016673A1 (en) Method of producing olefins and feedstocks for use in olefin production from crude oil having low pentane insolubles and high hydrogen content
US2608470A (en) Conversion of hydrocarbon oil to diesel fuel and carbon black
US3369992A (en) Low pour point synthetic crude oil
CN114901786A (en) Process for producing light olefins from crude oil
RU2024586C1 (en) Process for treating heavy asphalthene-containing stock
US3786110A (en) Asphaltenes for inhibiting polymerization of pyrolysis products
US2454615A (en) Catalytic cracking of hydrocarbons
US3366702A (en) Preparation of unsaturated hydrocarbons by pyrolysis, and related compositions
US4235702A (en) Hydrocarbon processing
US4750984A (en) Method of producing asphalt
US3326796A (en) Production of electrode grade petroleum coke
JPH0144272B2 (en)
US3338818A (en) Process for converting asphaltenecontaining hydrocarbon feeds
US4240898A (en) Process for producing high quality pitch
US2626892A (en) Cracking residual fractions containing salts
US3537976A (en) Process for preparing binder pitches
US2937135A (en) Extraction of polynuclear aromatic materials
US2220714A (en) Production of asphalt
US4009094A (en) Stabilizing pyrolysis naphtha
US2802798A (en) High grade paving asphalt and method of making same

Legal Events

Date Code Title Description
AS Assignment

Owner name: MARATHON OIL COMPANY, AN OH CORP

Free format text: ASSIGNS THE ENTIRE INTEREST IN ALL PATENTS AS OF JULY 10,1982 EXCEPT PATENT NOS. 3,783,944 AND 4,260,291. ASSIGNOR ASSIGNS A FIFTY PERCENT INTEREST IN SAID TWO PATENTS AS OF JULY 10,1982;ASSIGNOR:MARATHON PETROLEUM COMPANY;REEL/FRAME:004172/0421

Effective date: 19830420