GB439491A - Improvements in the recovery of valuable products from hydrocarbons - Google Patents
Improvements in the recovery of valuable products from hydrocarbonsInfo
- Publication number
- GB439491A GB439491A GB1613334A GB1613334A GB439491A GB 439491 A GB439491 A GB 439491A GB 1613334 A GB1613334 A GB 1613334A GB 1613334 A GB1613334 A GB 1613334A GB 439491 A GB439491 A GB 439491A
- Authority
- GB
- United Kingdom
- Prior art keywords
- naphthoquinone
- added
- product
- cracking
- addition
- 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
Links
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
- C07C7/14875—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound with organic 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)
Abstract
Diolefines are removed from crude hydrocarbons such as cracking products, benzine or benzol, by treatment with quinones, such as a -naphthoquinone, addition products being obtained. Cyclic dienes may be separately removed as similar addition products by effecting a first treatment at low temperatures, the acyclic dienes reacting usually above 50 DEG C.; moreover methylcyclopentadiene reacts more readily than cyclopentadiene. The quinones may be added in separate portions, each followed by separation of the addition product. The addition products are anthraquinone derivatives, and may be used as initial materials for the production of dyes. In examples: (1) a fraction of a cracking product of brown coal low temperature tar is treated with a -naphthoquinone and distilled under reduced pressure, the addition product of the quinone with cyclic dienes may be crystallized from methanol or ligroin; (2) a fraction of a cracking product of Panhandle oil is fractionally treated with a -naphthoquinone, the mixture being distilled after the first treatment, and successive additions being made to the successive distillates; the residues contain addition products of methylcyclopentadiene, a mixture of addition products of methylcyclopentadiene and cyclopentadiene, and the addition product of cyclopentadiene respectively; (3) a -naphthoquinone is added to the distillate free from cyclic dienes as in example 2, the addition product of acyclic dienes being obtained; (4) a -naphthoquinone is added to the first runnings of crude benzene from gasworks; (5) a cracking product freed from cyclic dienes is heated at 100 DEG C. under pressure with portions of a -naphthoquinone; (6) chloranil is added to the initial cracking product used in example 5, addition products of methylcyclopentadiene and cyclopentadiene being obtained; (7) benzoquinone is added to the initial cracking product used in example 5, biscyclopentadienequinone being obtained. Specification 320,375, [Class 2 (iii)], is referred to.ALSO:Diolefines are removed from crude hydrocarbons such as cracking products, benzine or benzol, by treatment with quinones, such as a -naphthoquinone, addition products being obtained. Cyclic diones may be separately removed as similar addition products by effecting a first treatment at low temperatures, the acyclic dienes reacting usually above 50 DEG C.; moreover methylcyclopentadiene reacts more readily than cyclopentadiene. The quinones may be added in separate portions, each followed by a separation of the addition product. In examples: (1) a fraction of a cracking-product of brown coal low temperature tar is treated with a -naphthoquinone and distilled under reduced pressure; (2) a fraction of a cracking product of Panhandle oil is fractionally treated with a -naphthoquinone, the mixture being distilled after the first treatment, and successive additions being made to the successive distillates. The residues contain addition products of methylcyclopentadiene and cyclopentadiene; (3) a -naphthaquinone is added to the distillate free from cyclic dienes as in example 2, the addition product of acyclic dienes being obtained; (4) a -naphthoquinone is added to the first runnings of crude benzene from gas works; (5) a cracking product freed from cyclic dienes is heated at 100 DEG C., under pressure with portions of a -naphthoquinone; (6) chloranil is added to the initial cracking product used in example 5; (7) benzoquinone is added to the initial cracking product used in example 5. Specification 320,375, [Class 2 (iii)], is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1613334A GB439491A (en) | 1934-05-30 | 1934-05-30 | Improvements in the recovery of valuable products from hydrocarbons |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1613334A GB439491A (en) | 1934-05-30 | 1934-05-30 | Improvements in the recovery of valuable products from hydrocarbons |
Publications (1)
Publication Number | Publication Date |
---|---|
GB439491A true GB439491A (en) | 1935-12-02 |
Family
ID=10071770
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1613334A Expired GB439491A (en) | 1934-05-30 | 1934-05-30 | Improvements in the recovery of valuable products from hydrocarbons |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB439491A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104817420A (en) * | 2015-04-08 | 2015-08-05 | 深圳市广昌达石油添加剂有限公司 | Method for extracting dicyclopentadiene in ethylene cracking C9 |
-
1934
- 1934-05-30 GB GB1613334A patent/GB439491A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104817420A (en) * | 2015-04-08 | 2015-08-05 | 深圳市广昌达石油添加剂有限公司 | Method for extracting dicyclopentadiene in ethylene cracking C9 |
CN104817420B (en) * | 2015-04-08 | 2016-07-06 | 深圳市广昌达石油添加剂有限公司 | A kind of extract the method for dicyclopentadiene in cracking of ethylene C9 |
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