US1441341A - Process for the recovery of aromatic compounds - Google Patents
Process for the recovery of aromatic compounds Download PDFInfo
- Publication number
- US1441341A US1441341A US248908A US24890818A US1441341A US 1441341 A US1441341 A US 1441341A US 248908 A US248908 A US 248908A US 24890818 A US24890818 A US 24890818A US 1441341 A US1441341 A US 1441341A
- Authority
- US
- United States
- Prior art keywords
- compounds
- aromatic
- aromatic compounds
- recovery
- boiling point
- 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
Links
- 150000001491 aromatic compounds Chemical class 0.000 title description 15
- 238000000034 method Methods 0.000 title description 9
- 238000011084 recovery Methods 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 description 15
- 238000009835 boiling Methods 0.000 description 12
- 239000000203 mixture Substances 0.000 description 8
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 4
- 239000012188 paraffin wax Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000004508 fractional distillation Methods 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical class C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- -1 compound hydrocarbons Chemical class 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000006396 nitration reaction Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/148—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
Definitions
- My process relates to the'recovery of aromatic compounds from mixtures or solutions of same with saturated or unsaturated non-aromatic hydrocarbons.
- a fraction obtained from distillation of the product derived from crackingCalifornia petroleum, such fraction distilling between 108 and 112 C. and containing some unsaturated hydrocarbon compounds and other compounds of the paraffin series is subjected to heat treatment in a tube furnace at a temperature of approximately 525 C. and a pressure of about 500 lbs. T'histemperature and pressure is such that the aromatic compounds are not changed but the unsaturated compounds and the compounds of the parafl'in series are changed in the treatment to either lower boiling pointc-ompounds' or higher boiling point compounds.
- the product of the heat treatment is then subjected to fractional (listillation and the desired aromatic compounds recovered substantially free from contaminating compounds.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Water Supply & Treatment (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Patented an. e, 1923.
errata STATES rnanc'is x. GOVERS, or NEW YORK, n. Y.
PROCESS FOR THE RECOVERY OF AROMATIC COMPOUNDS.
No Drawing.
To all whom it may concern:
Be it known that I, FRANCIS X. Govnns, residing at 800 Riverside Drive, borough of Manhattan, city, county, and State of New York, a citizen of the United States, have invented certain new and useful Improvements in Processes for the Recovery of Aromatic Compounds, of which the following is a specification. i
My process relates to the'recovery of aromatic compounds from mixtures or solutions of same with saturated or unsaturated non-aromatic hydrocarbons.
Inthe breaking down of high boiling point hydrocarbonsof the paraffin or naphthene series into aromatic hydrocarbons, there are formed at the same time a number of parafiins and unsaturated hydrocarbons of the same or approximately the sameboiL' ing points as the aromatic compounds sought for. These unsaturated compounds and compounds of the paraffin. series are difficult, if not impossible, to separate from the aromatic hydrocarbons desired by fractional distillation and while by treatmentwith acid andsubsequent treatment with caustic-soda and washing the unsaturated compounds may be eliminated, they are frequently present to such an extent as to require a very largeamount of acid for their removal. The presence of either unsaturated compounds or co-m-' pounds of the paraffin series with aromatic compounds interferes with many uses of such compounds; for example in the manu facture of explosives, it seriously hinders the process .of nitration and certain amounts of both or either of these compounds make it, if not impossible to nitrate, at least a dangerous undertaking. I have found that a quick and easy method of separating both unsaturated compounds and paraflin compounds from the aromatic hydrocarbons wanted is to subject the mixture to fractional distillation, and take fractions around the boiling point of the hydrocarbon desired; for instance, in case benzol is wanted, a cut may be taken from .78? to 82 C. and in case toluol is wanted, a cut from 108 to 112 C. The respective cut or cuts so made are then subjected to aheat treatment advantageously under pressure. This heat Application filed August 8, 1918. Serial No. 248,908.
treatment is so conducted in reference to the lower compound hydrocarbons and then the,
aromatic compound desired, leaving behind th: high boiling point'polymerized produc s.
The following. is an example of the foregoing process: A fraction obtained from distillation of the product derived from crackingCalifornia petroleum, such fraction distilling between 108 and 112 C. and containing some unsaturated hydrocarbon compounds and other compounds of the paraffin series is subjected to heat treatment in a tube furnace at a temperature of approximately 525 C. and a pressure of about 500 lbs. T'histemperature and pressure is such that the aromatic compounds are not changed but the unsaturated compounds and the compounds of the parafl'in series are changed in the treatment to either lower boiling pointc-ompounds' or higher boiling point compounds. The product of the heat treatment is then subjected to fractional (listillation and the desired aromatic compounds recovered substantially free from contaminating compounds. It will be obvious from the foregoing that many variations may be made in the details of operation without departing from the spirit and scope of my invention.
What I claim is:
1. In the process of purifying an aromatic compound in a mixture of substantially uniform boiling point containing ,it and contaminating non-aromatic hydrocarbon compounds having substantially the same boiling' point, subjecting said mixture to heat treatment under conditions of temperature and pressure such as to change the contaminating substances to compounds of higher or' lower boiling point without changing the aromatic compounds desired.
2. In the process of purifying aromatic compounds in mixture containing them and contaminating non-aromatic hydrocarbon compounds having substantially the same boiling points as the respective aromatic compounds desired, subjecting the mixture to fractional distillation to obtain mixtures of substantially uniform boiling point of the respective aromatic compounds with contaminating non-aromatic compoundshaving substantially similar boiling points and subjecting the respective mixtures to heat treatment under conditions of temperature and pressure such as to change the contaminating substances to compounds of higher or lower boiling point Without changing the aromatic compounds desired.
FRANCIS X. GO-VERS.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US248908A US1441341A (en) | 1918-08-08 | 1918-08-08 | Process for the recovery of aromatic compounds |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US248908A US1441341A (en) | 1918-08-08 | 1918-08-08 | Process for the recovery of aromatic compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1441341A true US1441341A (en) | 1923-01-09 |
Family
ID=22941201
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US248908A Expired - Lifetime US1441341A (en) | 1918-08-08 | 1918-08-08 | Process for the recovery of aromatic compounds |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1441341A (en) |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2415541A (en) * | 1944-02-19 | 1947-02-11 | United Gas Improvement Co | High-boiling aromatic oil |
| US2421615A (en) * | 1943-12-28 | 1947-06-03 | Standard Oil Dev Co | Treating hydrocarbon fluids |
| US2423374A (en) * | 1943-05-01 | 1947-07-01 | United Gas Improvement Co | Process for producing aromatics and diolefins from petroleum |
| US2430096A (en) * | 1943-12-16 | 1947-11-04 | Sun Oil Co | Plural stage catalytic and thermal conversion of hydrocarbons |
| US2431515A (en) * | 1943-12-24 | 1947-11-25 | Standard Oil Dev Co | Production of an aromatic gasoline |
| US2434395A (en) * | 1942-03-17 | 1948-01-13 | California Research Corp | Preparation of pure aromatics from petroleum distillates |
| US2436618A (en) * | 1944-12-27 | 1948-02-24 | Standard Oil Dev Co | Conversion of hydrocarbon oils |
| US2442060A (en) * | 1943-05-06 | 1948-05-25 | Standard Oil Dev Co | Production of aromatic hydrocarbons of high purity |
| US2680707A (en) * | 1948-05-22 | 1954-06-08 | Houilleres Ets | Method of treating mineral coal distillation benzol |
| US2701267A (en) * | 1955-02-01 | Resins | ||
| US2717912A (en) * | 1950-10-02 | 1955-09-13 | Martin R Kroger | Process and apparatus for the purification of benzene |
| US2766308A (en) * | 1952-03-21 | 1956-10-09 | Universal Oil Prod Co | Method for producing and recovering aromatic hydrocarbons |
| US2775629A (en) * | 1953-12-11 | 1956-12-25 | Exxon Research Engineering Co | Production of aromatics and dehydrogenated hydrocarbons |
| US2786020A (en) * | 1952-11-19 | 1957-03-19 | Richfield Oil Corp | Purification of toluic acids |
-
1918
- 1918-08-08 US US248908A patent/US1441341A/en not_active Expired - Lifetime
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2701267A (en) * | 1955-02-01 | Resins | ||
| US2434395A (en) * | 1942-03-17 | 1948-01-13 | California Research Corp | Preparation of pure aromatics from petroleum distillates |
| US2423374A (en) * | 1943-05-01 | 1947-07-01 | United Gas Improvement Co | Process for producing aromatics and diolefins from petroleum |
| US2442060A (en) * | 1943-05-06 | 1948-05-25 | Standard Oil Dev Co | Production of aromatic hydrocarbons of high purity |
| US2430096A (en) * | 1943-12-16 | 1947-11-04 | Sun Oil Co | Plural stage catalytic and thermal conversion of hydrocarbons |
| US2431515A (en) * | 1943-12-24 | 1947-11-25 | Standard Oil Dev Co | Production of an aromatic gasoline |
| US2421615A (en) * | 1943-12-28 | 1947-06-03 | Standard Oil Dev Co | Treating hydrocarbon fluids |
| US2415541A (en) * | 1944-02-19 | 1947-02-11 | United Gas Improvement Co | High-boiling aromatic oil |
| US2436618A (en) * | 1944-12-27 | 1948-02-24 | Standard Oil Dev Co | Conversion of hydrocarbon oils |
| US2680707A (en) * | 1948-05-22 | 1954-06-08 | Houilleres Ets | Method of treating mineral coal distillation benzol |
| US2717912A (en) * | 1950-10-02 | 1955-09-13 | Martin R Kroger | Process and apparatus for the purification of benzene |
| US2766308A (en) * | 1952-03-21 | 1956-10-09 | Universal Oil Prod Co | Method for producing and recovering aromatic hydrocarbons |
| US2786020A (en) * | 1952-11-19 | 1957-03-19 | Richfield Oil Corp | Purification of toluic acids |
| US2775629A (en) * | 1953-12-11 | 1956-12-25 | Exxon Research Engineering Co | Production of aromatics and dehydrogenated hydrocarbons |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US1441341A (en) | Process for the recovery of aromatic compounds | |
| US2586889A (en) | Separation of straight-chain from branched-chain hydrocarbons | |
| US2391404A (en) | Process for the separation of an unsaturated hydrocarbon from a hydrocarbon mixture | |
| US2456561A (en) | Azeotropic separation of xylene isomers | |
| US1882978A (en) | Recovery of unsaturated aliphatic hydrocarbons | |
| US2589621A (en) | Mesitylene manufacture | |
| US2002394A (en) | Process for converting hydrocarbons | |
| US2231241A (en) | Amplified distillation | |
| US2372941A (en) | Process for concentrating diolefins in mixtures containing same | |
| US1324143A (en) | Heots | |
| US3005032A (en) | Solvent extraction of naphthalenic from non-naphthalenic aromatic hydrocarbons using dimethyl sulfoxide | |
| US2799629A (en) | Separation of hydrocarbons | |
| US2000410A (en) | Treatment of hydrocarbon oils | |
| US2602817A (en) | Extraction of dimethylacetamide | |
| US2377221A (en) | Styrene separation | |
| US2382119A (en) | Process for extraction of hydrocarbons | |
| US2084471A (en) | Process of treating lubricating oils with selective solvents | |
| US3075025A (en) | Process for separating acetylenic compounds from an isoprene mixture | |
| US1683405A (en) | Iwan ostromislensky | |
| US2426821A (en) | Azeotropic distillation of five carbon diolefins in the presence of methyl formate | |
| US2537459A (en) | Recovery of pure hydrocarbons by extractive distillation | |
| US2506858A (en) | Azeotropic distillation of hydrocarbons with tetrahydrofuran | |
| US2411346A (en) | Refining of nitriles | |
| US2009554A (en) | Process of producing pure mercaptans | |
| US2408922A (en) | Separation of diolefins by azeotropic distillation |