JPS6256789B2 - - Google Patents
Info
- Publication number
- JPS6256789B2 JPS6256789B2 JP55098627A JP9862780A JPS6256789B2 JP S6256789 B2 JPS6256789 B2 JP S6256789B2 JP 55098627 A JP55098627 A JP 55098627A JP 9862780 A JP9862780 A JP 9862780A JP S6256789 B2 JPS6256789 B2 JP S6256789B2
- Authority
- JP
- Japan
- Prior art keywords
- organic solvent
- cobalt
- oxo
- aqueous
- pressure
- 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
- 229910017052 cobalt Inorganic materials 0.000 claims description 56
- 239000010941 cobalt Substances 0.000 claims description 56
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 43
- 239000003054 catalyst Substances 0.000 claims description 40
- 238000000034 method Methods 0.000 claims description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 29
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 28
- 239000003960 organic solvent Substances 0.000 claims description 28
- 238000000605 extraction Methods 0.000 claims description 23
- 150000001336 alkenes Chemical class 0.000 claims description 20
- 239000008346 aqueous phase Substances 0.000 claims description 18
- 238000006243 chemical reaction Methods 0.000 claims description 18
- UMYVESYOFCWRIW-UHFFFAOYSA-N cobalt;methanone Chemical compound O=C=[Co] UMYVESYOFCWRIW-UHFFFAOYSA-N 0.000 claims description 16
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 16
- 239000007864 aqueous solution Substances 0.000 claims description 15
- 230000015572 biosynthetic process Effects 0.000 claims description 14
- 239000007789 gas Substances 0.000 claims description 13
- 238000003786 synthesis reaction Methods 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 12
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 229940011182 cobalt acetate Drugs 0.000 claims description 8
- QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical group [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 claims description 8
- 150000007524 organic acids Chemical class 0.000 claims description 8
- 239000012071 phase Substances 0.000 claims description 8
- 239000000284 extract Substances 0.000 claims description 7
- 150000007522 mineralic acids Chemical class 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 238000007037 hydroformylation reaction Methods 0.000 claims description 4
- 239000004435 Oxo alcohol Substances 0.000 claims description 2
- 238000004821 distillation Methods 0.000 claims description 2
- PFQLIVQUKOIJJD-UHFFFAOYSA-L cobalt(ii) formate Chemical compound [Co+2].[O-]C=O.[O-]C=O PFQLIVQUKOIJJD-UHFFFAOYSA-L 0.000 claims 1
- 230000001590 oxidative effect Effects 0.000 claims 1
- 238000000638 solvent extraction Methods 0.000 claims 1
- 239000000047 product Substances 0.000 description 36
- 150000001868 cobalt Chemical class 0.000 description 15
- -1 cobalt Chemical class 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- 239000012074 organic phase Substances 0.000 description 6
- 238000004064 recycling Methods 0.000 description 6
- 239000000344 soap Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000003570 air Substances 0.000 description 5
- 230000003197 catalytic effect Effects 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 125000000129 anionic group Chemical group 0.000 description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 4
- 238000005810 carbonylation reaction Methods 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 230000006315 carbonylation Effects 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N methylene hexane Natural products CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- LHEFLUZWISWYSQ-CVBJKYQLSA-L cobalt(2+);(z)-octadec-9-enoate Chemical compound [Co+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O LHEFLUZWISWYSQ-CVBJKYQLSA-L 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 239000002815 homogeneous catalyst Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- DRHABPMHZRIRAH-UHFFFAOYSA-N 2,4,4,6,6-pentamethylhept-2-ene Chemical group CC(C)=CC(C)(C)CC(C)(C)C DRHABPMHZRIRAH-UHFFFAOYSA-N 0.000 description 1
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 229910004373 HOAc Inorganic materials 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 239000006286 aqueous extract Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001722 carbon compounds Chemical class 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 238000004523 catalytic cracking Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- SFJBWZNTPHYOEH-UHFFFAOYSA-N cobalt Chemical compound [Co].[Co].[Co] SFJBWZNTPHYOEH-UHFFFAOYSA-N 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- MQIKJSYMMJWAMP-UHFFFAOYSA-N dicobalt octacarbonyl Chemical group [Co+2].[Co+2].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-] MQIKJSYMMJWAMP-UHFFFAOYSA-N 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000002638 heterogeneous catalyst Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000004230 steam cracking Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- 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
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/04—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts
-
- 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
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/20—Carbonyls
-
- 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
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/40—Regeneration or reactivation
- B01J31/4015—Regeneration or reactivation of catalysts containing metals
- B01J31/4023—Regeneration or reactivation of catalysts containing metals containing iron group metals, noble metals or copper
- B01J31/403—Regeneration or reactivation of catalysts containing metals containing iron group metals, noble metals or copper containing iron group metals or copper
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/16—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxo-reaction combined with reduction
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/76—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
- C07C29/86—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by liquid-liquid treatment
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/88—Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/49—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
- C07C45/50—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
-
- 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
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
- B01J2231/32—Addition reactions to C=C or C-C triple bonds
- B01J2231/321—Hydroformylation, metalformylation, carbonylation or hydroaminomethylation
-
- 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
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/84—Metals of the iron group
- B01J2531/845—Cobalt
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/059,474 US4255279A (en) | 1979-07-20 | 1979-07-20 | Dual demetalling of oxo products with catalyst recycle |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5617640A JPS5617640A (en) | 1981-02-19 |
| JPS6256789B2 true JPS6256789B2 (enEXAMPLES) | 1987-11-27 |
Family
ID=22023184
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9862780A Granted JPS5617640A (en) | 1979-07-20 | 1980-07-18 | Double demetalizing method of oxooproduct being accompanied by recirculation of catalyst |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4255279A (enEXAMPLES) |
| JP (1) | JPS5617640A (enEXAMPLES) |
| CA (1) | CA1133514A (enEXAMPLES) |
| DE (1) | DE3026900A1 (enEXAMPLES) |
| GB (1) | GB2055371B (enEXAMPLES) |
| NL (1) | NL188520C (enEXAMPLES) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4459365A (en) * | 1981-05-29 | 1984-07-10 | Mitsubishi Gas Chemical Company, Inc. | Method of recovering a catalytic metal |
| US4404119A (en) * | 1981-12-23 | 1983-09-13 | Exxon Research & Engineering Co. | Process for recovery of cobalt oxo catalysts |
| US4400299A (en) * | 1981-12-23 | 1983-08-23 | Exxon Research & Engineering Co. | Oxidative recovery of cobalt oxo catalysts |
| US4419195A (en) * | 1982-01-07 | 1983-12-06 | Exxon Research & Engineering Co. | Electrolytic recovery of cobalt oxo catalysts |
| US4401834A (en) * | 1982-06-01 | 1983-08-30 | Exxon Research & Engineering Co. | Process for producing alcohols |
| GB8430225D0 (en) * | 1984-11-30 | 1985-01-09 | Exxon Research Engineering Co | Hydroformylation catalyst removal |
| GB8907577D0 (en) * | 1989-04-04 | 1989-05-17 | Exxon Chemical Patents Inc | Catalyst recovery in the production of alcohols |
| SG47945A1 (en) * | 1992-05-29 | 1998-04-17 | Exxon Chemical Patents Inc | Catalyst regeneration |
| US5237105A (en) * | 1992-05-29 | 1993-08-17 | Exxon Chemical Patents Inc. | Method for removing hydroformylation catalyst |
| GB9211880D0 (en) * | 1992-06-04 | 1992-07-15 | Exxon Chemical Patents Inc | Method and apparatus for the recovery of metal catalysts |
| US5321168A (en) * | 1993-09-16 | 1994-06-14 | Exxon Chemical Patents Inc. | Activation of cobalt preformer catalyst for oxo process |
| US5434318A (en) * | 1994-03-23 | 1995-07-18 | Exxon Chemical Patents Inc. | Reactivation or regeneration of cobalt preformer catalyst for oxo process |
| US5406006A (en) * | 1994-05-24 | 1995-04-11 | Exxon Chemical Patents Inc | Method for preparing a preformer catalyst via in-situ activation |
| US5545766A (en) * | 1994-09-30 | 1996-08-13 | Shell Oil Company | Cobalt-catalyzed process for preparing 1,3-propanediol using a lipophilic bidentate phosphine promotor |
| US5463146A (en) * | 1994-09-30 | 1995-10-31 | Shell Oil Company | Process for preparing 1,3-propanediol |
| US5463144A (en) * | 1994-09-30 | 1995-10-31 | Shell Oil Company | Process for preparing 1,3-propanediol |
| US5585528A (en) * | 1994-09-30 | 1996-12-17 | Shell Oil Company | Cobalt-catalyzed process for preparing 1,3-propanediol using a lipophilic tertiary amine promoter |
| US5545767A (en) * | 1994-09-30 | 1996-08-13 | Shell Oil Company | Process for preparing 1,3-propanediol |
| US5576471A (en) * | 1994-09-30 | 1996-11-19 | Shell Oil Company | Cobalt-catalyzed process for preparing 1,3-propanediol using a lipophilic dihydroxyarene promoter |
| US5463145A (en) * | 1994-09-30 | 1995-10-31 | Shell Oil Company | Process for preparing 1,3-propanediol |
| US5545765A (en) * | 1994-09-30 | 1996-08-13 | Shell Oil Company | Cobalt-catalyzed process for preparing 1,3-propanediol using a lipophilic quaternary arsonium salt promoter |
| US5777182A (en) * | 1994-09-30 | 1998-07-07 | Shell Oil Company | Cobalt-catalyzed process for preparing 1,3-propanidiol |
| US5981808A (en) * | 1994-09-30 | 1999-11-09 | Shell Oil Company | Cobalt-catalyzed process for preparing 1, 3-propanediol from etylene oxide |
| US5770776A (en) * | 1994-09-30 | 1998-06-23 | Shell Oil Company | Process for preparing 1,3-propanediol |
| US5563302A (en) * | 1994-09-30 | 1996-10-08 | Shell Oil Company | Cobalt-catalyzed process for preparing 1,3-propanediol using a lipophilic phosphine oxide promoter |
| DE59703815D1 (de) * | 1996-09-20 | 2001-07-26 | Basf Ag | Verfahren zur hydroformylierung |
| DE10009207A1 (de) | 2000-02-26 | 2001-08-30 | Oxeno Olefinchemie Gmbh | Verbessertes Verfahren zur Hydroformylierung von Olefinen durch Reduzierung der Ameisensäurekonzentration |
| AU2003212316A1 (en) * | 2002-03-15 | 2003-09-29 | Oxeno Olefinchemie Gmbh | Method for the hydroformylation of olefins |
| TW200642745A (en) | 2005-02-03 | 2006-12-16 | Shell Int Research | Process for inhibiting deposition of solids from a gaseous stream |
| TW200732292A (en) | 2006-02-01 | 2007-09-01 | Shell Int Research | A method of treating an aldehyde mixture, use of the treated aldehyde, and an alcohol |
| WO2008128852A1 (en) * | 2007-04-18 | 2008-10-30 | Exxonmobil Chemical Patents Inc. | Improvements in oxidative demetalling |
| WO2008145672A1 (en) * | 2007-05-30 | 2008-12-04 | Shell Internationale Research Maatschappij B.V. | Process for the removal of catalyst degradation products |
| CN102137834B (zh) * | 2008-08-29 | 2013-09-25 | 埃克森美孚化学专利公司 | 烯烃加氢甲酰化中的废气净化 |
| WO2010022881A1 (en) * | 2008-08-29 | 2010-03-04 | Exxonmobil Chemical Patents Inc. | Hydroformylation process including catalyst recycle |
| CN109894147B (zh) * | 2019-02-21 | 2022-03-11 | 中科合成油技术股份有限公司 | 一种负载型钴基催化剂及其制备方法和使用方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2767048A (en) * | 1951-09-07 | 1956-10-16 | Exxon Research Engineering Co | Preparation of metallic hydrocarbonyls |
| US2816933A (en) * | 1952-02-09 | 1957-12-17 | Exxon Research Engineering Co | Catalyst regeneration in oxo alcohol synthesis |
| US2744936A (en) * | 1952-02-09 | 1956-05-08 | Exxon Research Engineering Co | Oxo synthesis using cobalt salt of cobalt carbonyl |
| US2757205A (en) * | 1952-04-30 | 1956-07-31 | Exxon Research Engineering Co | Oxo process-acid decobalting in presence of carbon monoxide |
| US2751403A (en) * | 1952-12-31 | 1956-06-19 | Exxon Research Engineering Co | Catalyst recovery from alcohol synthesis process |
| US2757377A (en) * | 1953-03-02 | 1956-07-31 | Exxon Research Engineering Co | Acid decobalting |
| DE2139630C3 (de) * | 1971-08-07 | 1979-03-22 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von vorwiegend geradkettigen Aldehyden |
| US4061687A (en) * | 1971-12-30 | 1977-12-06 | Chemische Werke Huls Aktiengesellschaft | Oxo process with recovery of cobalt hydrocarbonyl in solution for recycle |
| DE2237373C3 (de) * | 1972-07-29 | 1981-12-10 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von vorwiegend geradkettigen Aldehyden |
| DE2244373A1 (de) | 1972-09-09 | 1974-04-04 | Basf Ag | Verfahren zur kontinuierlichen herstellung von waessrigen loesungen von kobaltcarbonylen |
| DE2332638C2 (de) * | 1973-06-27 | 1982-03-18 | Basf Ag, 6700 Ludwigshafen | Verfahren zur kontinuierlichen Herstellung von Lösungen von Kobaltcarbonyl und Kobaltcarbonylwasserstoff in organischen Lösungsmitteln |
-
1979
- 1979-07-20 US US06/059,474 patent/US4255279A/en not_active Expired - Lifetime
-
1980
- 1980-05-23 CA CA352,568A patent/CA1133514A/en not_active Expired
- 1980-07-16 DE DE19803026900 patent/DE3026900A1/de active Granted
- 1980-07-18 GB GB8023601A patent/GB2055371B/en not_active Expired
- 1980-07-18 JP JP9862780A patent/JPS5617640A/ja active Granted
- 1980-07-21 NL NLAANVRAGE8004184,A patent/NL188520C/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE3026900C2 (enEXAMPLES) | 1990-02-22 |
| CA1133514A (en) | 1982-10-12 |
| NL188520B (nl) | 1992-02-17 |
| US4255279A (en) | 1981-03-10 |
| NL188520C (nl) | 1992-07-16 |
| JPS5617640A (en) | 1981-02-19 |
| GB2055371A (en) | 1981-03-04 |
| GB2055371B (en) | 1983-08-10 |
| DE3026900A1 (de) | 1981-02-12 |
| NL8004184A (nl) | 1981-01-22 |
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