US2226378A - Oxidation of hydrocarbons - Google Patents
Oxidation of hydrocarbons Download PDFInfo
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- US2226378A US2226378A US286615A US28661539A US2226378A US 2226378 A US2226378 A US 2226378A US 286615 A US286615 A US 286615A US 28661539 A US28661539 A US 28661539A US 2226378 A US2226378 A US 2226378A
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- oxidation
- hydrocarbon
- aldehydes
- hydrocarbons
- acids
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C27/00—Processes involving the simultaneous production of more than one class of oxygen-containing compounds
- C07C27/10—Processes involving the simultaneous production of more than one class of oxygen-containing compounds by oxidation of hydrocarbons
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- This invention relates to a new and improved process for the preparation of chemical compounds by the oxidation of aliphatic hydrocarbons in the presence of a catalyst, and more par- 5 ticularly to such a process wherein the reaction products comprise aliphatic alcohols, aldehydes and acids.
- the higher aldehydes of the aliphatic series have considerable value as chemical compounds and a number of them have found use in industry as perfumes.
- the difliculties in the way of preparing such compounds have kept their costs so high as to limit their field of usefulness.
- An improved and simpler method of obtaining such aldehydes would make more accessible a very desirable class of products.
- the same condition holds in the case of a number of the higher aliphatic alcohols and acids also, for example those containing in the neighborhood of 8 to 12 95 carbon atoms.
- An object of our invention is an improved method for the production of alcohols, aldehydes, and acids by the incomplete oxidation of allphatic hydrocarbons.
- a further object is such a process in which carefully controlled conditions allow a high degree of efliciency in the preparation of the desired products.
- a still further object is a process in which the several products obtained may be separated in relatively pure form. Additional object will be disclosed as the process is further described hereinafter.
- the process of our invention which comprises introducing a normally liquid hydrocarbon in the vapor phase into a heated chamber, together with an oxidizing agent comprising a gas containing free oxygen.
- the oxidation step is carried out in the presence of benzoyl peroxide as a catalyst.
- the mixed gases and vapors are subjected to a temperature between 250 and 500 C. While the oxidation of the hydrocabons constitutes an exothermic reaction, the heat evolved will not be suflicient to maintain the desired temperature and external heating will be necessary. It is essential that the reactionperiod be kept at a relatively short time interval, and we have found 15 seconds to be the maximum allowable time.
- reaction period 86 not greater than 12 seconds, in order that the oxidation may not proceed too far.
- the reacting materials and reaction products are removed from the heated chamber while still in the vapor phase and are. condensed by any desired method and apparatus under such conditions and in such 6 an atmosphere that further reaction cannot take place.
- the amount of hydrocarbon will be above the explosive limit in all cases.
- the accompanying drawing shows diagrammatically a flow sheet of one method of carrying Q out our process.
- the normally liquid hydrocarbon is forced through conduit 2 into the preheater 3.
- the gas containing free oxygen is passed through conduit 4 through the preheater 3, en route to the reaction chamas her 5.
- Both the vaporized hydrocarbon and the oxygen containing gas pass into the reaction chamber 5 where they become intimately mixed and where a temperature of 250 to 500 C. is maintained, vjsaid catalyst, promoting partial go oxidation, being present, whereby partial oxidation of the hydrocarbons is brought about.
- the vapors pass out the conduit 6 into separator l, where any tar formed in the process is separated out.
- the mixed vapors and gases then pass as through condenser 8, where the products capable of condensation become liquefied.
- the liquid condensate flows into reservoir 9, while a second vessel l0 receives any further condensed product not caught in chamber 9, but condensed in ii.
- the reservoirs 9 and it contain the liquefied unreacted hydrocarbon that has passed through the process, and also condensed water and the alcohols, aldehydes and acids resulting from the oxidation process. Such alcohols, aldehydes and acids will commonly be found in the water-insoluble layer.
- Example One gram of benaoyl peroxide was dissolved in u Momoinaphtha. Thismixturewasvaporised intheusuaimannerandmixedwithairata temperature oi 887' C. The time oi reaction wassfiseconds andthepercentageoi'hydrocarbon in the reaction mixture was 18.7. The yield was approximately 16.84% aldehydes and 14.15% acids.
- the method of operation according to the present invention produces alcohols, aldehydes and acids. However, it is especially i'avorable to the production oi alcohols.
- the alcohols, aldehydes and acids resulting from the oxidation oi hydrocarbons according to the process of our invention are products 01' considerable economic value and 01' desirable properties, and the process described oii'ers a novel and advantageous method of obtaining such products.
- Our process is characterized by higher yields and greater efliciency than any process in the art.
- the alcohols, aldehydes and acids may be separated from the hydrocarbon condensate and from one mother by the use of suitable solvents.
- suitable solvents for example, a saturated solution oi. sodium bisulflte was found desirable for extraction, the bisulflte subsequently being made alkaline and beins subjected to steam distillation.
- the acids were desirably extracted by h orio acid.
- the process for producing partially oxidized products or normally liquid aliphatic hydrocarbons which comprises introducing said hydrocarbons in vapor phase, tosether with an oxidizing agent comprising a gas containing tree oxygen, into a reaction chamber at a temperature between 250 C. and 500 C., maintaining the amount of hydrocarbon in the hydrocarbon-oxygen ratio above the explosive limit, and reacting said materials for a period not exceeding 15 seconds in the presence of benzoyl peroxide.
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Description
Patented Dec. 24, 1940 UNITED STATES OXIDATION or nrnnocsanoms William H. m, New Orleans, 1..., and Clyde 0. Sheely, State College, Miss.
Original application April 2, 1938, Serial No.
199,636. 1939, 8erial No. 286,815
Divided and this application July :6,
1 Claim. (Cl. 260-451) This invention relates to a new and improved process for the preparation of chemical compounds by the oxidation of aliphatic hydrocarbons in the presence of a catalyst, and more par- 5 ticularly to such a process wherein the reaction products comprise aliphatic alcohols, aldehydes and acids.
This application is a continuation-in-part of our copending application Serial No. 108,478, filed October 30, 1936, now Patent No. 2,190,453, and
is a division of our copending application Serial No. 199,636, flied April 2, 1938.
The higher aldehydes of the aliphatic series have considerable value as chemical compounds and a number of them have found use in industry as perfumes. The difliculties in the way of preparing such compounds, however, have kept their costs so high as to limit their field of usefulness. An improved and simpler method of obtaining such aldehydes would make more accessible a very desirable class of products. The same condition holds in the case of a number of the higher aliphatic alcohols and acids also, for example those containing in the neighborhood of 8 to 12 95 carbon atoms.
An object of our invention is an improved method for the production of alcohols, aldehydes, and acids by the incomplete oxidation of allphatic hydrocarbons. A further object is such a process in which carefully controlled conditions allow a high degree of efliciency in the preparation of the desired products. A still further object is a process in which the several products obtained may be separated in relatively pure form. Additional object will be disclosed as the process is further described hereinafter.
We have found that the foregoing objects may be accomplished by the process of our invention which comprises introducing a normally liquid hydrocarbon in the vapor phase into a heated chamber, together with an oxidizing agent comprising a gas containing free oxygen. The oxidation step is carried out in the presence of benzoyl peroxide as a catalyst. Within the reaction chamber the mixed gases and vapors are subjected to a temperature between 250 and 500 C. While the oxidation of the hydrocabons constitutes an exothermic reaction, the heat evolved will not be suflicient to maintain the desired temperature and external heating will be necessary. It is essential that the reactionperiod be kept at a relatively short time interval, and we have found 15 seconds to be the maximum allowable time. Preferably we employ a reaction period 86 not greater than 12 seconds, in order that the oxidation may not proceed too far. The reacting materials and reaction products are removed from the heated chamber while still in the vapor phase and are. condensed by any desired method and apparatus under such conditions and in such 6 an atmosphere that further reaction cannot take place. The amount of hydrocarbon will be above the explosive limit in all cases. We have found it desirable to use an amount of hydrocarbon of at least 10% by volume of the gaseous reaction mix- 10 ture, and preferably between 20 and 40%.
It will be a desirable step in our process also to utilize the unreacted hydrocarbon resultin from the process and to recycle it to an additional similar oxidation step, whereby the ad- I. vantages of the presence of an excess of hydrocarbon are obtained with no loss in non-reacting material.
The accompanying drawing shows diagrammatically a flow sheet of one method of carrying Q out our process. From a reservoir i, the normally liquid hydrocarbon is forced through conduit 2 into the preheater 3. The gas containing free oxygen is passed through conduit 4 through the preheater 3, en route to the reaction chamas her 5. Both the vaporized hydrocarbon and the oxygen containing gas pass into the reaction chamber 5 where they become intimately mixed and where a temperature of 250 to 500 C. is maintained, vjsaid catalyst, promoting partial go oxidation, being present, whereby partial oxidation of the hydrocarbons is brought about. The vapors pass out the conduit 6 into separator l, where any tar formed in the process is separated out. The mixed vapors and gases then pass as through condenser 8, where the products capable of condensation become liquefied. The liquid condensate flows into reservoir 9, while a second vessel l0 receives any further condensed product not caught in chamber 9, but condensed in ii. The reservoirs 9 and it contain the liquefied unreacted hydrocarbon that has passed through the process, and also condensed water and the alcohols, aldehydes and acids resulting from the oxidation process. Such alcohols, aldehydes and acids will commonly be found in the water-insoluble layer.
Specific operating conditions suitable for our process for the production of alcohols, aldehydes, and acids are shown in the following example. 50 This is to be considered as merely illustrative, however, and not limiting in its application.
Example One gram of benaoyl peroxide was dissolved in u Momoinaphtha. Thismixturewasvaporised intheusuaimannerandmixedwithairata temperature oi 887' C. The time oi reaction wassfiseconds andthepercentageoi'hydrocarbon in the reaction mixture was 18.7. The yield was approximately 16.84% aldehydes and 14.15% acids.
The method of operation according to the present invention produces alcohols, aldehydes and acids. However, it is especially i'avorable to the production oi alcohols. The alcohols, aldehydes and acids resulting from the oxidation oi hydrocarbons according to the process of our invention, are products 01' considerable economic value and 01' desirable properties, and the process described oii'ers a novel and advantageous method of obtaining such products. Our process is characterized by higher yields and greater efliciency than any process in the art.
The alcohols, aldehydes and acids may be separated from the hydrocarbon condensate and from one mother by the use of suitable solvents. In the case of aldehydes, for example, a saturated solution oi. sodium bisulflte was found desirable for extraction, the bisulflte subsequently being made alkaline and beins subjected to steam distillation. The acids were desirably extracted by h orio acid.
Whileourprocesshaabeendescribedindetail in the foregoing, it will be understood that many variations in procedure may be employed without departing from the scope of our invention. In the example cited, a hydrocarbon traction oi a speciilo distillation range was used, but it would be a highly desirable procedure also to start with a single aliphatic hydrocarbon, ior example octane, or a mixture of octanes.
We wish to be limited, therefore, only by the following patent claim:
The process for producing partially oxidized products or normally liquid aliphatic hydrocarbons which comprises introducing said hydrocarbons in vapor phase, tosether with an oxidizing agent comprising a gas containing tree oxygen, into a reaction chamber at a temperature between 250 C. and 500 C., maintaining the amount of hydrocarbon in the hydrocarbon-oxygen ratio above the explosive limit, and reacting said materials for a period not exceeding 15 seconds in the presence of benzoyl peroxide.
WILLIAM H. ICING. CLYDE Q. BHEELY.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US286615A US2226378A (en) | 1938-04-02 | 1939-07-26 | Oxidation of hydrocarbons |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US199636A US2215472A (en) | 1938-04-02 | 1938-04-02 | Oxidation of hydrocarbons |
US286615A US2226378A (en) | 1938-04-02 | 1939-07-26 | Oxidation of hydrocarbons |
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US2226378A true US2226378A (en) | 1940-12-24 |
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US286615A Expired - Lifetime US2226378A (en) | 1938-04-02 | 1939-07-26 | Oxidation of hydrocarbons |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2469322A (en) * | 1945-08-22 | 1949-05-03 | Socony Vacuum Oil Co Inc | Oxidation of sulfuric acid heavy alkylate |
US2626277A (en) * | 1948-10-15 | 1953-01-20 | Cities Service Res & Dev Co | Oxidation of petroleum fractions |
US2714604A (en) * | 1952-09-04 | 1955-08-02 | Celanese Corp | Production of oxygenated hydrocarbons |
US2770637A (en) * | 1952-09-04 | 1956-11-13 | Celanese Corp | Production of oxygenated hydrocarbons |
US2774780A (en) * | 1952-09-11 | 1956-12-18 | Standard Oil Co | Oxidized oil product and process for the production thereof |
-
1939
- 1939-07-26 US US286615A patent/US2226378A/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2469322A (en) * | 1945-08-22 | 1949-05-03 | Socony Vacuum Oil Co Inc | Oxidation of sulfuric acid heavy alkylate |
US2626277A (en) * | 1948-10-15 | 1953-01-20 | Cities Service Res & Dev Co | Oxidation of petroleum fractions |
US2714604A (en) * | 1952-09-04 | 1955-08-02 | Celanese Corp | Production of oxygenated hydrocarbons |
US2770637A (en) * | 1952-09-04 | 1956-11-13 | Celanese Corp | Production of oxygenated hydrocarbons |
US2774780A (en) * | 1952-09-11 | 1956-12-18 | Standard Oil Co | Oxidized oil product and process for the production thereof |
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