GB1420446A - Inhibitors for olefin complexing process - Google Patents
Inhibitors for olefin complexing processInfo
- Publication number
- GB1420446A GB1420446A GB2602473A GB2602473A GB1420446A GB 1420446 A GB1420446 A GB 1420446A GB 2602473 A GB2602473 A GB 2602473A GB 2602473 A GB2602473 A GB 2602473A GB 1420446 A GB1420446 A GB 1420446A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sorbent solution
- radicals
- cubf
- recovery
- separation
- 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
- 150000001336 alkenes Chemical class 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 2
- 230000000536 complexating effect Effects 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 title 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 abstract 4
- 239000002594 sorbent Substances 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 abstract 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 abstract 2
- 238000011084 recovery Methods 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 238000000926 separation method Methods 0.000 abstract 2
- ALLIZEAXNXSFGD-UHFFFAOYSA-N 1-methyl-2-phenylbenzene Chemical group CC1=CC=CC=C1C1=CC=CC=C1 ALLIZEAXNXSFGD-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- 239000002841 Lewis acid Substances 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 230000029936 alkylation Effects 0.000 abstract 1
- 238000005804 alkylation reaction Methods 0.000 abstract 1
- 125000000129 anionic group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000007517 lewis acids Chemical group 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000001477 organic nitrogen group Chemical group 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 150000003222 pyridines Chemical class 0.000 abstract 1
- 238000007086 side reaction Methods 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 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
- C07C7/152—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by forming adducts or complexes
- C07C7/156—Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by forming adducts or complexes with solutions of copper salts
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S585/00—Chemistry of hydrocarbon compounds
- Y10S585/949—Miscellaneous considerations
- Y10S585/952—Reaction stopping or retarding
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)
- Pyridine Compounds (AREA)
Abstract
1420446 Separating olefins from mixtures EXXON RESEARCH & ENG CO 31 May 1973 [2 June 1972] 26024/73 Heading C5E In a process for the separation and recovery of complexible olefins by contacting a feedstream with an aromatic sorbent solution containing a cuprous salt whose anionic component is a Lewis acid, alkylation and polymerization side reactions are reduced by incorporating an organic phosphine and an organic nitrogen base in the sorbent solution. The phosphine suitably has the formula R 1 R 2 R 3 P wherein R 1 , R 2 and R 3 are C 1-20 alkyl radicals, phenyl radicals, C 7-12 alkylaryl or aralkyl radicals. The nitrogen base can be an alkyl substituted pyridine, a tertiary alkyl amine or a tertiaryalkylarylamine. Suitable cuprous salts are CuPF 6 , CuBF 4 , CuBF 3 Cl, CuAlCl 4 , CuAlBr 4 , CuTaF 6 and CuAlClxBy (wherein x and y are integers whose -sum is 4). The sorbent solution can contain benzene, cumene or methyl biphenyl as the solvent. In the separation and recovery of ethylene or propylene the-feed can be contacted with the sorbent solution at 20-300 C. and 0À5-50 atm. abs.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US25921972A | 1972-06-02 | 1972-06-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1420446A true GB1420446A (en) | 1976-01-07 |
Family
ID=22984045
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2602473A Expired GB1420446A (en) | 1972-06-02 | 1973-05-31 | Inhibitors for olefin complexing process |
Country Status (6)
Country | Link |
---|---|
US (1) | US3758607A (en) |
JP (1) | JPS5715565B2 (en) |
CA (1) | CA999605A (en) |
DE (1) | DE2327599C2 (en) |
FR (1) | FR2186453B1 (en) |
GB (1) | GB1420446A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2138018A (en) * | 1983-03-19 | 1984-10-17 | Hidefumi Hirai | Process for the recovery of ethylene from gaseous mixtures |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0040916B1 (en) * | 1980-05-28 | 1983-10-12 | Tenneco Resins, Inc. | The separation of complexible ligands using alkylation inhibitors |
US4317950A (en) * | 1980-07-23 | 1982-03-02 | Tenneco Chemicals, Inc. | Use of amine-aluminum chloride adducts as alkylation inhibitors in a ligand-complexing process |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2566136A (en) * | 1943-11-06 | 1951-08-28 | Standard Oil Dev Co | Method of removing acetylenes from diolefin mixtures |
US2444945A (en) * | 1944-12-30 | 1948-07-13 | Standard Oil Dev Co | Diolefin extraction |
US2566137A (en) * | 1950-03-15 | 1951-08-28 | Standard Oil Dev Co | Removing acetylenes from hydrocarbon mixtures and improvements in the separation of butadiene and acetylenes |
US3265751A (en) * | 1964-12-17 | 1966-08-09 | Pennsalt Chemicals Corp | Inhibiting popcorn polymer formation |
US3420862A (en) * | 1965-01-04 | 1969-01-07 | Exxon Research Engineering Co | Complexes of copper compounds with acetylides |
-
1972
- 1972-06-02 US US00259219A patent/US3758607A/en not_active Expired - Lifetime
-
1973
- 1973-05-30 DE DE2327599A patent/DE2327599C2/en not_active Expired
- 1973-05-31 GB GB2602473A patent/GB1420446A/en not_active Expired
- 1973-06-01 FR FR7320105A patent/FR2186453B1/fr not_active Expired
- 1973-06-01 CA CA173,005A patent/CA999605A/en not_active Expired
- 1973-06-01 JP JP6176373A patent/JPS5715565B2/ja not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2138018A (en) * | 1983-03-19 | 1984-10-17 | Hidefumi Hirai | Process for the recovery of ethylene from gaseous mixtures |
Also Published As
Publication number | Publication date |
---|---|
DE2327599C2 (en) | 1982-09-30 |
JPS5715565B2 (en) | 1982-03-31 |
JPS4948604A (en) | 1974-05-11 |
CA999605A (en) | 1976-11-09 |
FR2186453A1 (en) | 1974-01-11 |
FR2186453B1 (en) | 1977-05-06 |
DE2327599A1 (en) | 1973-12-13 |
US3758607A (en) | 1973-09-11 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed [section 19, patents act 1949] | ||
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19920531 |