US3262983A - High temperature reactions - Google Patents
High temperature reactions Download PDFInfo
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- US3262983A US3262983A US278993A US27899363A US3262983A US 3262983 A US3262983 A US 3262983A US 278993 A US278993 A US 278993A US 27899363 A US27899363 A US 27899363A US 3262983 A US3262983 A US 3262983A
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/0006—Controlling or regulating processes
- B01J19/002—Avoiding undesirable reactions or side-effects, e.g. avoiding explosions, or improving the yield by suppressing side-reactions
- B01J19/0026—Avoiding carbon deposits
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/76—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation of hydrocarbons with partial elimination of hydrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C4/00—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms
- C07C4/08—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms by splitting-off an aliphatic or cycloaliphatic part from the molecule
- C07C4/10—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms by splitting-off an aliphatic or cycloaliphatic part from the molecule from acyclic hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
- C07C5/327—Formation of non-aromatic carbon-to-carbon double bonds only
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
- C07C5/327—Formation of non-aromatic carbon-to-carbon double bonds only
- C07C5/333—Catalytic processes
- C07C5/3332—Catalytic processes with metal oxides or metal sulfides
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- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12861—Group VIII or IB metal-base component
- Y10T428/12951—Fe-base component
- Y10T428/12958—Next to Fe-base component
- Y10T428/12965—Both containing 0.01-1.7% carbon [i.e., steel]
Definitions
- This invention relates to an improved method of performing high temperature hydrocarbon reactions. More particularly, this invention relates to an improved material for containing high temperature hydrocarbon reactions.
- Typical of the processes in which carbon formation poses a problem are pyrolysis reactions such as the pyrolysis of benzene and its homologues to form polyaryls, the pyrolysis of paraffins to form ethylene, propylene, butadiene, and the like, the pyrolysis of various alkylabenzenes to produce styrene and its derivatives, the pyrolysis of various olefins, parafiines, or mixtures thereof to produce diolefins, and like pyrolysis reactions.
- reactors be constructed of steels which contain from about 11 to about 30 percent chromium and a maximum of about 1.5 percent nickel. Included within this composition range are steels of the A181 400 series stainless steels. Examples of such AISI 400 series stainless steels and their nominal compositions (percent, balance iron) are as follows:
- nickel or cobalt-containing steels have good high temperature properties, they are generally unsuitable for use as reactor materials in high temperature reaction processes.
- reactors are usually fabricated of tubing of the desired size and length and which may be formed in a coil. Further, a plurality of reactor tubes may be manifolded to a header in order to give additional capacity. For this and other reasons, metallurgical bonding between reaction contacting surface and supporting metal is required.
- AISI 400 series stainless steels in general do not have particularly good mechanical properties (strength) at temperatures over about 550 degrees centigrade.
- pyrolysis reactions are run at temperatures of from about 700 to about 900 degrees centigrade in order to obtain an eflicient conversion of feed to the desired product, although certain materials may react at slightly lower temperatures.
- the temperature of the reactor metal may be more than 100 degrees centigrade higher than the reaction temperature in situations where the reaction is generally endothermic and heat must be supplied from outside the reactor as by a gas furnace or an electric heater.
- a number of well known steels have good mechanical properties (strength) at temperatures above about 550 degrees centigrade as contemplated by the present invention.
- a substantial number of these high temperature steels contain nickel or cobalt usually in an amount greater than about 3 percent. It has been observed, how- A better understanding of the present invention may be obtained in light of the following examples which are set forth to illustrate, and are not to be construed to limit, the present invention.
- Example 1 1 AISI-TP304 steel has a nominal composition of 0.08 percent maximum carbon, 2.00 percent maximum manganese, from 0.03 to 0.04 percent maximum phosphorus, 0.03 percent maximum sulfur, 0.75 percent maximum silicon, from about 18 to about 20 percent chromium, from about 8 to about 11 percent nickel, and the balance iron.
- Example 2 Propylene and steam were fed to the reactor of Example 1 at rates of about 425 and 1100 grams per hour, respectively. Temperature of the unpacked reaction zone was varied from about 700 to about 850 degrees centi- .grade. centigrade a product containing about 1.6 percent by weight ethylene was obtained. 'When the temperature of the reaction zone was increased to about 850 degrees centigrade, the amount of ethylene in the product increased to about 33.7 percent by weight.
- Example 3 Kerosene and steam were [fed to the reactor of Example 1 at rates of about 420 and 1100 grams per ⁇ hour, respectively. Temperature of the unpacked reaction zone was varied from about 750 to about 900 degrees centilgrade. At a temperature of about 700 degrees centigrade, a product containing about 17.4 percent by weigh-t ethylene was obtained. At temperatures of about 850 and 900 degrees centigrade, product containing about 33.7 and 30 weight percent ethylene, respectively, was obtained.
- Example 4 Ethylbenzene and steam were fed to the reactor of Example 1 at rates of about 495 and 1100 grams per hour, respectively. Temperature of the unpacked reaction zone was varied from about 600 to about 900 degrees centigrade. The best conversion was obtained at a temperature of about 850 degrees centigrade, the product containing about 31.6 percent by weight styrene.
- Example 5 A self regenerative catalyst of the potassium and chromium promoted Fe O type was positioned in the previously unpacked reaction zone of the reactor used in the previous examples. Ethylbenzene and steam were fed to the reactor at rates of about 490 and 1100 grams per hour, respectively. The reaction zone (containing catalyst) was maintained at a temperature of about 570 degrees centigrade. A product containing about 44 percent by weight styrene was obtained.
- Example 6 To the catalyst-containing reactor of Example 5 were fed butene-l and steam at rates of about 420 and 1200 grams per hour, respectively. The reaction zone was maintained at a temperature of about 600 degrees centigrade. Product containing about 19 percent by weight butadiene was obtained.
- Example 7 Using the reactor of Example 1, other high tempera ture hydrocarbon reactions, such as oxidation, synthesis, dehydration, and the like wherein a hydrocarbon is vaporized and subjected to high temperatures, may be performed with similar freedom from carbon formation in the reactor.
- the improvement which comprises carrying out the reaction in a reactor having a reaction contacting surface of a steel selected from the groups consisting of those having AISI designations of TP405, TP410, TP430, TP443, and TP446, such steel being metallurgically bonded to a supporting second steel which has good strength at temperatures above about 550 degrees centigrade.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
United States Patent 3,267.38?) HIGH TEMPERATURE REACTIONS Raymond J. Ladd, Midland, and Frederick J. 'Soderquist,
Essexviile, Mich, assignors to The Dow Chemical Company, Midland, Mich, a corporation of Delaware N0 Drawing. Filed May 8, 1963, Ser. No. 278,993 7 Claims. (Cl. 260669) This invention relates to an improved method of performing high temperature hydrocarbon reactions. More particularly, this invention relates to an improved material for containing high temperature hydrocarbon reactions.
A common phenomenon associated with processes in which hydrocarbons are heated to high temperatures in a reactor, as, for example, to accomplish partial or controlled pyrolysis, is the formation of carbon. Formation of carbon results in a loss of useful product materials. Accumulation of carboin within reactors employed in hydrocarbon pyrolysis lowers efficiency and may be sufii cient to entirely block fiow within the reactor. Undesirable formation and subsequent accumulation of carbon within reactors employed in high temperature hydrocarbon processes has plagued the industry for years. Typical of the processes in which carbon formation poses a problem are pyrolysis reactions such as the pyrolysis of benzene and its homologues to form polyaryls, the pyrolysis of paraffins to form ethylene, propylene, butadiene, and the like, the pyrolysis of various alkylabenzenes to produce styrene and its derivatives, the pyrolysis of various olefins, parafiines, or mixtures thereof to produce diolefins, and like pyrolysis reactions.
As a solution to the problem of carbon formation in high temperature hydrocarbon reactions, it has been suggested that reactors be constructed of steels which contain from about 11 to about 30 percent chromium and a maximum of about 1.5 percent nickel. Included within this composition range are steels of the A181 400 series stainless steels. Examples of such AISI 400 series stainless steels and their nominal compositions (percent, balance iron) are as follows:
ever, that the presence of nickel or cobalt in a steel in excess of about 1.5 percent tends to catalyze carbon formation. Thus, while nickel or cobalt-containing steels have good high temperature properties, they are generally unsuitable for use as reactor materials in high temperature reaction processes.
We have discovered that the dual problems of high temperature strength and carbon fromation can be solved by providing a composite reactor having an A181 400 series stainless steel surface exposed to the pyrolysis reaction, said AISI 400 series steel surface metallurgically bonded to a supporting steel having good high temperature strength such as a steel designated as one of the AISI 300 series. In this manner, benefit is obtained from the high temperature properties of the chromium-nickel steel, while maintaining carbon formation and accumulation at a minimum. Metallurgical bonding may be accomplished as by co-extrusion of the two metal portions while applying an appropriate amount of heat. Metallurgical bonding is a true molecular or atomic bonding between oxide-free surfaces of dissimilar metals.
Because of space considerations, reactors are usually fabricated of tubing of the desired size and length and which may be formed in a coil. Further, a plurality of reactor tubes may be manifolded to a header in order to give additional capacity. For this and other reasons, metallurgical bonding between reaction contacting surface and supporting metal is required.
Without metallurgical bonding between reaction contacting surface and support metal, fabrication of the reactor is usually beset by problems such as separation of the two component parts, or collapse of the inner reactor surface during bending operations. In use, non-metallurgically bonded composites tend to suffer from distortion due to differences in thermal expansion characteristics of the metals. Thermal distortion of a cyclic nature can cause eventual rupture of the reaction contacting surface, the support metal or both. When nonmetallurgically bonded composite tubing, for example, is manifolded to a common header, bimetallic distortion tends to loosen and eventually destroy the joints,
AISI C Max. Mn Max. Si Max. Cr Ni Max. P Max S Max. Other 0. 08 1.00 0. 75 11. 5-13. 5 0.50 0. 03-0. 04 0. 03 Al 0.10-0.30. 0. l5 1. 00 0. 75 11. 5-13. 5 0. 0. 03-0. 04 0. 03 0. l2 1. 00 0. 75 14. 0-18. 0 0. 50 0. 03-0. 04 0. 03 0. 20 1.00 0.75 18. 0-23. 0 0.50 0. 03-0. 04 0. 03 Cu 0.90125 0. 20 1.50 0.75 23. 030. 0 O. 50 0. 03-0. 04 0.03 N 0 10-025 Although the use of A181 400 series stainless steels for reactors solves the problem of carbon formation, another problem manifests itself. AISI 400 series stainless steels in general do not have particularly good mechanical properties (strength) at temperatures over about 550 degrees centigrade. Ordinarily, pyrolysis reactions, as contemplated by the present invention, are run at temperatures of from about 700 to about 900 degrees centigrade in order to obtain an eflicient conversion of feed to the desired product, although certain materials may react at slightly lower temperatures. The temperature of the reactor metal may be more than 100 degrees centigrade higher than the reaction temperature in situations where the reaction is generally endothermic and heat must be supplied from outside the reactor as by a gas furnace or an electric heater.
A number of well known steels have good mechanical properties (strength) at temperatures above about 550 degrees centigrade as contemplated by the present invention. A substantial number of these high temperature steels contain nickel or cobalt usually in an amount greater than about 3 percent. It has been observed, how- A better understanding of the present invention may be obtained in light of the following examples which are set forth to illustrate, and are not to be construed to limit, the present invention.
Example 1 1 AISI-TP304 steel has a nominal composition of 0.08 percent maximum carbon, 2.00 percent maximum manganese, from 0.03 to 0.04 percent maximum phosphorus, 0.03 percent maximum sulfur, 0.75 percent maximum silicon, from about 18 to about 20 percent chromium, from about 8 to about 11 percent nickel, and the balance iron.
With the unpacked zone of the reactor tube maintained at a temperature of about 800 degrees centigrade, benzene and steam were fed to the reactor at rates of about 425 and 450 grams per hour, respectively, for a period of about twenty hours. After removal of the steam, the product obtained contained about 9.5 percent by weight of diphenyl and terphenyls.
After discontinuance of the run, the unpacked reaction zone was examined for carbon formation and build up. No measurable quantity of carbon was found.
Example 2 Propylene and steam were fed to the reactor of Example 1 at rates of about 425 and 1100 grams per hour, respectively. Temperature of the unpacked reaction zone was varied from about 700 to about 850 degrees centi- .grade. centigrade a product containing about 1.6 percent by weight ethylene was obtained. 'When the temperature of the reaction zone was increased to about 850 degrees centigrade, the amount of ethylene in the product increased to about 33.7 percent by weight.
After about five hours of operation, no measurable quantity of carbon had formed or built up inside the reactor.
Example 3 Kerosene and steam were [fed to the reactor of Example 1 at rates of about 420 and 1100 grams per \hour, respectively. Temperature of the unpacked reaction zone was varied from about 750 to about 900 degrees centilgrade. At a temperature of about 700 degrees centigrade, a product containing about 17.4 percent by weigh-t ethylene was obtained. At temperatures of about 850 and 900 degrees centigrade, product containing about 33.7 and 30 weight percent ethylene, respectively, was obtained.
After about eight hours of operation, no measurable quantity of carbon had formed or accumulated within the reactor.
Example 4 Ethylbenzene and steam were fed to the reactor of Example 1 at rates of about 495 and 1100 grams per hour, respectively. Temperature of the unpacked reaction zone was varied from about 600 to about 900 degrees centigrade. The best conversion was obtained at a temperature of about 850 degrees centigrade, the product containing about 31.6 percent by weight styrene.
After about fourteen hours of operation, no measurable quantity of carbon had formed or accumulated in the reactor.
Example 5 A self regenerative catalyst of the potassium and chromium promoted Fe O type was positioned in the previously unpacked reaction zone of the reactor used in the previous examples. Ethylbenzene and steam were fed to the reactor at rates of about 490 and 1100 grams per hour, respectively. The reaction zone (containing catalyst) was maintained at a temperature of about 570 degrees centigrade. A product containing about 44 percent by weight styrene was obtained.
After about '210 hours of operation no measurable quantity of carbon had formed or accumulated.
Example 6 To the catalyst-containing reactor of Example 5 were fed butene-l and steam at rates of about 420 and 1200 grams per hour, respectively. The reaction zone was maintained at a temperature of about 600 degrees centigrade. Product containing about 19 percent by weight butadiene was obtained.
Inspection after about two and one-half hours of operation indicated that no measurable quantity of carbon had formed or accumulated.
At a reaction temperature of about 700 degrees- 4 Example 7 Using the reactor of Example 1, other high tempera ture hydrocarbon reactions, such as oxidation, synthesis, dehydration, and the like wherein a hydrocarbon is vaporized and subjected to high temperatures, may be performed with similar freedom from carbon formation in the reactor.
Various modifications may be made "in the present invention without departing from the spirit or scope there of, and it is to be understood that we limit ourselves only as defined in the appended claims.
We claim:
1. In a method of performing high temperature reactions wherein hydrocarbon vapors are subjected to temperatures above 500 degrees centigrade, the improvement which comprises carrying out the reaction in a reactor having a reaction contacting surface of a steel containing from about 11 to about 30 percent chromium and a maximum of about 1.5 percent nickel, such steel being metallurgically bonded to a supporting second steel which has good strength at temperatures above about 550 degrees centigrade.
2. In a method of performing high temperature reactions wherein hydrocarbon vapors are subjected to temperatures above 500 degrees centigrade, the improvement which comprises carrying out the reaction in a reactor having a reaction contacting surface of a steel selected from the groups consisting of those having AISI designations of TP405, TP410, TP430, TP443, and TP446, such steel being metallurgically bonded to a supporting second steel which has good strength at temperatures above about 550 degrees centigrade.
3. In a method of performing high temperature reactions wherein hydrocarbon vapors are subjected to temperatures above 550 degrees centigrade, the improvement which comprises carrying out the reaction in a reactor having a reaction contacting surface of a steel having the A181 designation TP405, such steel being metallurgically bonded to a supporting second steel which has good strength at temperatures above about 550 degrees centigrade.
4. In a method of performing high temperature reactions wherein hydrocarbons vapors are subjected to temperatures above 500 degrees centigrade, the improvement which comprises carrying out the reaction in a reactor having a reaction contacting surface of a steel having the A181 designation TP410, such steel being metallurgically bonded to a supporting second steel which has good strength at temperatures above about 550 degrees centigrade.
5. In a method of performing high temperature reactions wherein hydrocarbon vapors are subjected to temperatures above 550 degrees centigrade, the improvement which comprises carrying out the reation in a reactor having a reaction contacting surface of a steel having the A181 designation TP430, such steel being metallurgically bonded to a supporting second steel which has good strength at temperatures above about 550 degrees centigrade.
6. In a method of performing high temperature reactions wherein hydrocarbon vapors are subjected to temperatures above 500 degrees centigrade, the improvement which comprises carrying out the reaction in a reactor having a reaction contacting surface of a steel having the A181 designation 'FP443, such steel being metallurgically bonded to a supporting second steel which has good strength at temperatures above about 550 degrees centigrade.
7. In a method of performing high temperature reactions wherein hydrocarbon vapors are subjected to temperatures above 500 degrees centigrade, the improvement which comprises carrying out the reaction in a reactor having a reaction contacting surface of a steel having the A151 designation TP446, such steel being metallurgi- 5 6 cally bonded to a supporting second steel which has good OTHER REFERENCES strength at temperatures above about 55 0 degrees centi- Archer; High Chromium Alloys in the Refinery, rade. finer & Natural Gasoline Manufacturer, vol. 20, No. 7, July 1941, pp. 66-85 (pp. 68 and 69 particularly relied References Cited by the Examiner 5 P UNITED STATES PATENTS DELBERT E. GANTZ, Primaly Examiner.
1,938,609 12/ 1 933 Reilly 260-670 C. R. DAVIS, Assistant Examiner.
Claims (1)
1. IN A METHOD OF PERFORMING HIGH TEMPERATURE REACTIONS WHEREIN HYDROCARBON VAPORS ARE SUBJECTED TO TEMPERATURES ABOVE 500 DEGREES CENTIGRADE, THE IMPROVEMENT WHICH COMPRISES CARRYING OUT THE REACTION IN A REACTOR HAVING A REACTION CONTACTING SURFACE OF A STEEL CONTAINING FROM ABOUT 11 TO ABOUT 30 PERCENT CHROMIUM AND A MAXIMUM OF ABOUT 1.5 PERCENT NICKEL, SUCH STEEL BEING METALLURGICALLY BONDED TO A SUPPORTING SECOND STEEL WHICH HAS GOOD STRENGTH AT TEMPERATURES ABOVE ABOUT 550 DEGREES CENTIGRADE.
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Application Number | Priority Date | Filing Date | Title |
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US278993A US3262983A (en) | 1963-05-08 | 1963-05-08 | High temperature reactions |
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US278993A US3262983A (en) | 1963-05-08 | 1963-05-08 | High temperature reactions |
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US3262983A true US3262983A (en) | 1966-07-26 |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3474153A (en) * | 1967-06-16 | 1969-10-21 | Union Carbide Corp | Dehydrogenation of ethylbenzene to styrene |
US3475508A (en) * | 1967-12-14 | 1969-10-28 | Badger Co | Dehydrogenation of alkyl aromatic compounds in the presence of nickelbearing alloy steels |
DE3231045A1 (en) * | 1981-08-21 | 1983-03-03 | Kubota Ltd., Osaka | REACTION TUBE FOR THERMAL CLEAVING OR REFORMING HYDROCARBONS AND METHOD FOR THE PRODUCTION THEREOF |
FR2518565A1 (en) * | 1981-12-23 | 1983-06-24 | Toyo Engineering Corp | TUBE FOR THERMAL CRACKING OR REFORMING OF HYDROCARBONS |
US4444732A (en) * | 1982-05-14 | 1984-04-24 | Kubota Ltd | Tube for thermal cracking or reforming of hydrocarbon |
US4444731A (en) * | 1981-02-25 | 1984-04-24 | Kubota Ltd. | Tube for thermal cracking or reforming hydrocarbon |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1938609A (en) * | 1932-04-15 | 1933-12-12 | Dow Chemical Co | Production of diphenyl from benzene |
-
1963
- 1963-05-08 US US278993A patent/US3262983A/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1938609A (en) * | 1932-04-15 | 1933-12-12 | Dow Chemical Co | Production of diphenyl from benzene |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3474153A (en) * | 1967-06-16 | 1969-10-21 | Union Carbide Corp | Dehydrogenation of ethylbenzene to styrene |
US3475508A (en) * | 1967-12-14 | 1969-10-28 | Badger Co | Dehydrogenation of alkyl aromatic compounds in the presence of nickelbearing alloy steels |
US4444731A (en) * | 1981-02-25 | 1984-04-24 | Kubota Ltd. | Tube for thermal cracking or reforming hydrocarbon |
DE3231045A1 (en) * | 1981-08-21 | 1983-03-03 | Kubota Ltd., Osaka | REACTION TUBE FOR THERMAL CLEAVING OR REFORMING HYDROCARBONS AND METHOD FOR THE PRODUCTION THEREOF |
US4510988A (en) * | 1981-08-21 | 1985-04-16 | Kubota Ltd. | Tube for thermal cracking or reforming hydrocarbon and manufacturing method thereof |
FR2518565A1 (en) * | 1981-12-23 | 1983-06-24 | Toyo Engineering Corp | TUBE FOR THERMAL CRACKING OR REFORMING OF HYDROCARBONS |
DE3247568A1 (en) * | 1981-12-23 | 1983-06-30 | Kubota Ltd., Osaka | REACTOR TUBE FOR THERMAL CRACKING OR REFORMING HYDROCARBONS |
US4444732A (en) * | 1982-05-14 | 1984-04-24 | Kubota Ltd | Tube for thermal cracking or reforming of hydrocarbon |
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