BE534300A - - Google Patents
Info
- Publication number
- BE534300A BE534300A BE534300DA BE534300A BE 534300 A BE534300 A BE 534300A BE 534300D A BE534300D A BE 534300DA BE 534300 A BE534300 A BE 534300A
- Authority
- BE
- Belgium
- Prior art keywords
- alcohol
- oxygen
- process according
- oxidation
- primary
- Prior art date
Links
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 48
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 30
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 29
- 239000001301 oxygen Substances 0.000 claims description 29
- 229910052760 oxygen Inorganic materials 0.000 claims description 29
- 230000003647 oxidation Effects 0.000 claims description 24
- 238000007254 oxidation reaction Methods 0.000 claims description 24
- 239000007789 gas Substances 0.000 claims description 23
- 238000000034 method Methods 0.000 claims description 22
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical group O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 17
- 229910001882 dioxygen Inorganic materials 0.000 claims description 17
- 150000003138 primary alcohols Chemical class 0.000 claims description 13
- 150000003333 secondary alcohols Chemical class 0.000 claims description 13
- 239000011541 reaction mixture Substances 0.000 claims description 12
- 239000007795 chemical reaction product Substances 0.000 claims description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 239000003701 inert diluent Substances 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000001307 helium Substances 0.000 claims description 2
- 229910052734 helium Inorganic materials 0.000 claims description 2
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 description 16
- 239000000203 mixture Substances 0.000 description 9
- 150000001298 alcohols Chemical class 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 238000007792 addition Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 241000254173 Coleoptera Species 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- -1 amyl alcohols Chemical group 0.000 description 1
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical group OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 229940093476 ethylene glycol Drugs 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000011551 heat transfer agent Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B15/00—Peroxides; Peroxyhydrates; Peroxyacids or salts thereof; Superoxides; Ozonides
- C01B15/01—Hydrogen peroxide
- C01B15/022—Preparation from organic compounds
- C01B15/026—Preparation from organic compounds from alcohols
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE534300A true BE534300A (https=) |
Family
ID=165711
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE534300D BE534300A (https=) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE534300A (https=) |
-
0
- BE BE534300D patent/BE534300A/nl unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5817868A (en) | Method and devices for controlling the oxidation of a hydrocarbon to an acid by regulating temperature/conversion relationship in multi-stage arrangements | |
| US3530185A (en) | Oxidation process | |
| US9067864B2 (en) | Process for producing aromatic amines | |
| EP0274681B1 (en) | Process for production of acrylic acid | |
| US4353843A (en) | Preparation of nitrite esters | |
| US6057483A (en) | High selective method of phenol and acetone production | |
| TWI440620B (zh) | 氣相中製備異氰酸酯之方法 | |
| US20130189164A1 (en) | Process For Downstream Recovery Of Nitroalkane Using Dividing Wall Column | |
| US10377690B1 (en) | Method for catalytic production of refined enal products from an aldehyde feed stream using a single enclosed unit | |
| JP3490459B2 (ja) | メチルメルカプトプロパナールの製造方法 | |
| US5616784A (en) | Thermal cleavage of carbamic esters | |
| JP2023100734A (ja) | 不飽和カルボン酸エステルの製造方法 | |
| EP1042264A4 (en) | HIGHLY SELECTIVE METHOD FOR PRODUCING PHENOL AND ACETONE | |
| JP2004510686A (ja) | メチルホルメートの連続的製造方法 | |
| FR2617475A1 (fr) | Synthese du chloro-1 difluoro-1,1 ethane | |
| US3003853A (en) | Production of hydrogen peroxide | |
| EP0738699B1 (en) | Method for producing 1,2-dichloroethane | |
| BE534300A (https=) | ||
| US3405172A (en) | Preparation of acrylic acid with the prevention of formation of acrylic polymers | |
| US9518006B2 (en) | Method for producing diaminotoluene | |
| US5908589A (en) | Methods for separating catalyst from oxidation mixtures containing dibasic acids | |
| US4110406A (en) | Preparation of 1-chloro-2-trifluoromethyl-3,3,3-trifluoropropene from isobutylene | |
| US4110407A (en) | Preparation of 1-chloro-2-trifluoromethyl-3,3,3-trifluoropropene from isobutane | |
| US6129875A (en) | Process of separating catalyst from oxidation mixtures | |
| DE69526263T2 (de) | Oxydation von sekundären Alkoholen |