GB1240858A - Process for the preparation of ketones and/or aldehydes from olefins - Google Patents
Process for the preparation of ketones and/or aldehydes from olefinsInfo
- Publication number
- GB1240858A GB1240858A GB4730968A GB4730968A GB1240858A GB 1240858 A GB1240858 A GB 1240858A GB 4730968 A GB4730968 A GB 4730968A GB 4730968 A GB4730968 A GB 4730968A GB 1240858 A GB1240858 A GB 1240858A
- Authority
- GB
- United Kingdom
- Prior art keywords
- suspension
- stannic
- support material
- oxide
- silica
- 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 2
- 150000002576 ketones Chemical class 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 238000002360 preparation method Methods 0.000 title abstract 2
- 150000001299 aldehydes Chemical class 0.000 title 1
- 239000000725 suspension Substances 0.000 abstract 13
- 239000000463 material Substances 0.000 abstract 11
- 239000000203 mixture Substances 0.000 abstract 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 10
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 8
- 239000003054 catalyst Substances 0.000 abstract 7
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Inorganic materials O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 abstract 7
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 abstract 6
- 239000000377 silicon dioxide Substances 0.000 abstract 5
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 abstract 4
- -1 hydroxyl ions Chemical class 0.000 abstract 4
- 229910052742 iron Inorganic materials 0.000 abstract 4
- 239000011135 tin Substances 0.000 abstract 4
- 229910052718 tin Inorganic materials 0.000 abstract 4
- 239000010936 titanium Substances 0.000 abstract 4
- 229910052719 titanium Inorganic materials 0.000 abstract 4
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 abstract 3
- 238000001354 calcination Methods 0.000 abstract 3
- 150000002500 ions Chemical class 0.000 abstract 3
- 229910052750 molybdenum Inorganic materials 0.000 abstract 3
- 239000011733 molybdenum Substances 0.000 abstract 3
- 239000007787 solid Substances 0.000 abstract 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 abstract 3
- 229910052721 tungsten Inorganic materials 0.000 abstract 3
- 239000010937 tungsten Substances 0.000 abstract 3
- 229910052720 vanadium Inorganic materials 0.000 abstract 3
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 abstract 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- 229910004298 SiO 2 Inorganic materials 0.000 abstract 2
- 229910006404 SnO 2 Inorganic materials 0.000 abstract 2
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 abstract 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 239000004202 carbamide Substances 0.000 abstract 2
- 238000001914 filtration Methods 0.000 abstract 2
- 239000002245 particle Substances 0.000 abstract 2
- 238000003756 stirring Methods 0.000 abstract 2
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 abstract 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000001816 cooling Methods 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 1
- 238000011065 in-situ storage Methods 0.000 abstract 1
- VLAPMBHFAWRUQP-UHFFFAOYSA-L molybdic acid Chemical compound O[Mo](O)(=O)=O VLAPMBHFAWRUQP-UHFFFAOYSA-L 0.000 abstract 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000002244 precipitate Substances 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
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 238000005406 washing Methods 0.000 abstract 1
Classifications
-
- 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
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
- C07C45/33—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
- C07C45/34—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
-
- 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
-
- 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
-
- 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
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
- C07C45/33—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
- C07C45/34—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
- C07C45/35—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds in propene or isobutene
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL6713663A NL6713663A (enrdf_load_stackoverflow) | 1967-10-07 | 1967-10-07 | |
NL6801921A NL144577B (nl) | 1967-10-07 | 1968-02-10 | Werkwijze voor het bereiden van butanon uit buteen. |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1240858A true GB1240858A (en) | 1971-07-28 |
Family
ID=26644246
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4730968A Expired GB1240858A (en) | 1967-10-07 | 1968-10-04 | Process for the preparation of ketones and/or aldehydes from olefins |
Country Status (9)
Country | Link |
---|---|
AT (2) | AT289745B (enrdf_load_stackoverflow) |
BE (1) | BE721863A (enrdf_load_stackoverflow) |
CH (1) | CH534006A (enrdf_load_stackoverflow) |
DE (1) | DE1801301C3 (enrdf_load_stackoverflow) |
ES (1) | ES358886A1 (enrdf_load_stackoverflow) |
FR (1) | FR1586033A (enrdf_load_stackoverflow) |
GB (1) | GB1240858A (enrdf_load_stackoverflow) |
NL (2) | NL6713663A (enrdf_load_stackoverflow) |
SE (1) | SE363623B (enrdf_load_stackoverflow) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004060843A1 (ja) * | 2003-01-06 | 2004-07-22 | Asahi Kasei Chemicals Corporation | アルコール及び/又はケトンの製造方法 |
KR100757719B1 (ko) | 2004-02-10 | 2007-09-11 | 마루젠 세끼유가가꾸 가부시키가이샤 | 알코올 및/또는 케톤의 제조 방법 |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL163764C (nl) * | 1969-11-12 | 1980-10-15 | Stamicarbon | Werkwijze voor het bereiden van alkanonen uit olefinen. |
-
1967
- 1967-10-07 NL NL6713663A patent/NL6713663A/xx unknown
-
1968
- 1968-02-10 NL NL6801921A patent/NL144577B/xx not_active IP Right Cessation
- 1968-10-04 CH CH1482968A patent/CH534006A/de not_active IP Right Cessation
- 1968-10-04 GB GB4730968A patent/GB1240858A/en not_active Expired
- 1968-10-04 DE DE19681801301 patent/DE1801301C3/de not_active Expired
- 1968-10-04 BE BE721863D patent/BE721863A/xx unknown
- 1968-10-05 ES ES358886A patent/ES358886A1/es not_active Expired
- 1968-10-07 AT AT976568A patent/AT289745B/de not_active IP Right Cessation
- 1968-10-07 AT AT00660/70A patent/AT294782B/de not_active IP Right Cessation
- 1968-10-07 FR FR1586033D patent/FR1586033A/fr not_active Expired
- 1968-10-07 SE SE1352768A patent/SE363623B/xx unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004060843A1 (ja) * | 2003-01-06 | 2004-07-22 | Asahi Kasei Chemicals Corporation | アルコール及び/又はケトンの製造方法 |
US7291755B2 (en) | 2003-01-06 | 2007-11-06 | Asahi Kasei Chemicals Corporation | Process for producing alcohol and/or ketone |
KR100757719B1 (ko) | 2004-02-10 | 2007-09-11 | 마루젠 세끼유가가꾸 가부시키가이샤 | 알코올 및/또는 케톤의 제조 방법 |
Also Published As
Publication number | Publication date |
---|---|
DE1801301A1 (de) | 1969-05-14 |
BE721863A (enrdf_load_stackoverflow) | 1969-04-04 |
CH534006A (de) | 1973-02-28 |
FR1586033A (enrdf_load_stackoverflow) | 1970-02-06 |
SE363623B (enrdf_load_stackoverflow) | 1974-01-28 |
AT289745B (de) | 1971-05-10 |
NL6713663A (enrdf_load_stackoverflow) | 1969-04-09 |
DE1801301B2 (de) | 1979-05-23 |
AT294782B (de) | 1971-11-15 |
ES358886A1 (es) | 1970-11-01 |
DE1801301C3 (de) | 1980-01-10 |
NL6801921A (enrdf_load_stackoverflow) | 1969-08-12 |
NL144577B (nl) | 1975-01-15 |
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