SE503573C2 - Förfarande för framställning av väteperoxid samt lösningsmedelsystem för användning i detta förfarande - Google Patents
Förfarande för framställning av väteperoxid samt lösningsmedelsystem för användning i detta förfarandeInfo
- Publication number
- SE503573C2 SE503573C2 SE9002713A SE9002713A SE503573C2 SE 503573 C2 SE503573 C2 SE 503573C2 SE 9002713 A SE9002713 A SE 9002713A SE 9002713 A SE9002713 A SE 9002713A SE 503573 C2 SE503573 C2 SE 503573C2
- Authority
- SE
- Sweden
- Prior art keywords
- carbamate
- solvent system
- formula
- groups
- hydrogen peroxide
- Prior art date
Links
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 title claims abstract description 26
- 238000000034 method Methods 0.000 title claims abstract description 24
- 239000002904 solvent Substances 0.000 title claims abstract description 22
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims abstract description 33
- 239000012224 working solution Substances 0.000 claims abstract description 29
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims abstract description 7
- 150000004056 anthraquinones Chemical class 0.000 claims abstract description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 7
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 6
- 238000004519 manufacturing process Methods 0.000 claims abstract 3
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 5
- JAHVNMPDEKINFF-UHFFFAOYSA-N 2-ethylhexyl n,n-dipentylcarbamate Chemical compound CCCCCN(CCCCC)C(=O)OCC(CC)CCCC JAHVNMPDEKINFF-UHFFFAOYSA-N 0.000 claims 2
- VBLNBASBINMWJE-UHFFFAOYSA-N 2-ethylhexyl n-butylcarbamate Chemical compound CCCCNC(=O)OCC(CC)CCCC VBLNBASBINMWJE-UHFFFAOYSA-N 0.000 claims 2
- 125000004122 cyclic group Chemical group 0.000 abstract description 2
- 238000000605 extraction Methods 0.000 description 16
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 9
- -1 alkyl chloroformate Chemical compound 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 150000002430 hydrocarbons Chemical group 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000011877 solvent mixture Substances 0.000 description 2
- SNDGLCYYBKJSOT-UHFFFAOYSA-N 1,1,3,3-tetrabutylurea Chemical compound CCCCN(CCCC)C(=O)N(CCCC)CCCC SNDGLCYYBKJSOT-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 101100370014 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) tof-1 gene Proteins 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- GTVWRXDRKAHEAD-UHFFFAOYSA-N Tris(2-ethylhexyl) phosphate Chemical compound CCCCC(CC)COP(=O)(OCC(CC)CCCC)OCC(CC)CCCC GTVWRXDRKAHEAD-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- NMRPBPVERJPACX-UHFFFAOYSA-N octan-3-ol Chemical compound CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 150000004040 pyrrolidinones Chemical class 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000003809 water extraction Methods 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
- C01B15/023—Preparation from organic compounds by the alkyl-anthraquinone process
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FI894411A FI82671C (fi) | 1989-09-18 | 1989-09-18 | Foerfarande foer framstaellning av vaeteperoxid och loesningsmedelssystem foer anvaendning i detta foerfarande. |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| SE9002713D0 SE9002713D0 (sv) | 1990-08-22 |
| SE9002713L SE9002713L (sv) | 1991-03-19 |
| SE503573C2 true SE503573C2 (sv) | 1996-07-08 |
Family
ID=8529011
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE9002713A SE503573C2 (sv) | 1989-09-18 | 1990-08-22 | Förfarande för framställning av väteperoxid samt lösningsmedelsystem för användning i detta förfarande |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US5114701A (ja) |
| JP (1) | JPH03112802A (ja) |
| CA (1) | CA2023696A1 (ja) |
| DE (1) | DE4026631A1 (ja) |
| FI (1) | FI82671C (ja) |
| FR (1) | FR2652074B1 (ja) |
| GB (1) | GB2236102B (ja) |
| SE (1) | SE503573C2 (ja) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998028225A1 (en) * | 1996-12-23 | 1998-07-02 | Kvaerner Process Systems A/S | Method for the production of hydrogen peroxide by hydrating a chinone solution and arrangement for performing the methods |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018102463A1 (en) * | 2016-11-30 | 2018-06-07 | Christopher Duke | Free radical-and reactive oxygen species-reacting compounds |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2041124A1 (de) * | 1970-08-19 | 1972-02-24 | Degussa | Verfahren zur Herstellung organischer Wasserstoffperoxidloesungen |
| US4046868A (en) * | 1973-09-26 | 1977-09-06 | E. I. Du Pont De Nemours And Company | Production of hydrogen peroxide |
| SE459919C (sv) * | 1987-03-27 | 1991-03-25 | Eka Nobel Ab | Foerfarande foer framstaellning av vaeteperoxid genom reduktion och oxidation av en antrakinon |
| FR2614015B1 (fr) * | 1987-04-16 | 1989-07-13 | Atochem | Procede de production cyclique de peroxyde d'hydrogene |
-
1989
- 1989-09-18 FI FI894411A patent/FI82671C/fi not_active IP Right Cessation
-
1990
- 1990-08-21 CA CA002023696A patent/CA2023696A1/en not_active Abandoned
- 1990-08-22 US US07/571,084 patent/US5114701A/en not_active Expired - Fee Related
- 1990-08-22 SE SE9002713A patent/SE503573C2/sv not_active IP Right Cessation
- 1990-08-23 DE DE4026631A patent/DE4026631A1/de not_active Withdrawn
- 1990-09-12 FR FR9011280A patent/FR2652074B1/fr not_active Expired - Fee Related
- 1990-09-17 JP JP2246961A patent/JPH03112802A/ja active Pending
- 1990-09-17 GB GB9020246A patent/GB2236102B/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1998028225A1 (en) * | 1996-12-23 | 1998-07-02 | Kvaerner Process Systems A/S | Method for the production of hydrogen peroxide by hydrating a chinone solution and arrangement for performing the methods |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH03112802A (ja) | 1991-05-14 |
| FI894411A0 (fi) | 1989-09-18 |
| SE9002713D0 (sv) | 1990-08-22 |
| FR2652074A1 (fr) | 1991-03-22 |
| GB9020246D0 (en) | 1990-10-31 |
| FI82671C (fi) | 1991-04-10 |
| FR2652074B1 (fr) | 1992-10-16 |
| DE4026631A1 (de) | 1991-03-28 |
| GB2236102A (en) | 1991-03-27 |
| GB2236102B (en) | 1993-07-07 |
| SE9002713L (sv) | 1991-03-19 |
| FI82671B (fi) | 1990-12-31 |
| CA2023696A1 (en) | 1991-03-19 |
| US5114701A (en) | 1992-05-19 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| NUG | Patent has lapsed |
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