FI65763C - Stabiliserade vattenloesningar av vaeteperoxid - Google Patents
Stabiliserade vattenloesningar av vaeteperoxid Download PDFInfo
- Publication number
- FI65763C FI65763C FI800660A FI800660A FI65763C FI 65763 C FI65763 C FI 65763C FI 800660 A FI800660 A FI 800660A FI 800660 A FI800660 A FI 800660A FI 65763 C FI65763 C FI 65763C
- Authority
- FI
- Finland
- Prior art keywords
- acid
- hydrogen peroxide
- liter
- hours
- solutions
- Prior art date
Links
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 43
- 239000000243 solution Substances 0.000 description 27
- 239000002253 acid Substances 0.000 description 25
- 239000003381 stabilizer Substances 0.000 description 23
- 238000012360 testing method Methods 0.000 description 17
- 238000000354 decomposition reaction Methods 0.000 description 10
- MGRVRXRGTBOSHW-UHFFFAOYSA-N (aminomethyl)phosphonic acid Chemical class NCP(O)(O)=O MGRVRXRGTBOSHW-UHFFFAOYSA-N 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- YDONNITUKPKTIG-UHFFFAOYSA-N [Nitrilotris(methylene)]trisphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CP(O)(O)=O YDONNITUKPKTIG-UHFFFAOYSA-N 0.000 description 8
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical class NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 7
- 230000015556 catabolic process Effects 0.000 description 6
- 238000006731 degradation reaction Methods 0.000 description 6
- 235000013905 glycine and its sodium salt Nutrition 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 150000002978 peroxides Chemical class 0.000 description 6
- 230000006641 stabilisation Effects 0.000 description 6
- 238000011105 stabilization Methods 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 229910002651 NO3 Inorganic materials 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 3
- 235000019820 disodium diphosphate Nutrition 0.000 description 3
- GYQBBRRVRKFJRG-UHFFFAOYSA-L disodium pyrophosphate Chemical compound [Na+].[Na+].OP([O-])(=O)OP(O)([O-])=O GYQBBRRVRKFJRG-UHFFFAOYSA-L 0.000 description 3
- 229940038485 disodium pyrophosphate Drugs 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000008139 complexing agent Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 235000011180 diphosphates Nutrition 0.000 description 2
- WJJMNDUMQPNECX-UHFFFAOYSA-N dipicolinic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=N1 WJJMNDUMQPNECX-UHFFFAOYSA-N 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000000546 pharmaceutical excipient Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 238000013112 stability test Methods 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- IHUWGKOYNDNJBN-UHFFFAOYSA-N 3-prop-2-ynyl-1,3-oxazol-2-one Chemical compound O=C1OC=CN1CC#C IHUWGKOYNDNJBN-UHFFFAOYSA-N 0.000 description 1
- 206010013496 Disturbance in attention Diseases 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 1
- 229910020212 Na2SnO3 Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- TVQLLNFANZSCGY-UHFFFAOYSA-N disodium;dioxido(oxo)tin Chemical compound [Na+].[Na+].[O-][Sn]([O-])=O TVQLLNFANZSCGY-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229960002449 glycine Drugs 0.000 description 1
- DKPHLYCEFBDQKM-UHFFFAOYSA-H hexapotassium;1-phosphonato-n,n-bis(phosphonatomethyl)methanamine Chemical compound [K+].[K+].[K+].[K+].[K+].[K+].[O-]P([O-])(=O)CN(CP([O-])([O-])=O)CP([O-])([O-])=O DKPHLYCEFBDQKM-UHFFFAOYSA-H 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- SAWKFRBJGLMMES-UHFFFAOYSA-N methylphosphine Chemical group PC SAWKFRBJGLMMES-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- -1 nitrate ions Chemical class 0.000 description 1
- 150000002926 oxygen Chemical class 0.000 description 1
- 229960003330 pentetic acid Drugs 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 229940079864 sodium stannate Drugs 0.000 description 1
- 229940071182 stannate Drugs 0.000 description 1
- 125000005402 stannate group Chemical group 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 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
- C01B15/037—Stabilisation by additives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7905600A FR2450783A1 (fr) | 1979-03-05 | 1979-03-05 | Solutions aqueuses stabilisees de peroxyde d'hydrogene |
| FR7905600 | 1979-03-05 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI800660A7 FI800660A7 (fi) | 1980-09-06 |
| FI65763B FI65763B (fi) | 1984-03-30 |
| FI65763C true FI65763C (fi) | 1984-07-10 |
Family
ID=9222748
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI800660A FI65763C (fi) | 1979-03-05 | 1980-03-04 | Stabiliserade vattenloesningar av vaeteperoxid |
Country Status (16)
| Country | Link |
|---|---|
| EP (1) | EP0015818B1 (Direct) |
| JP (1) | JPS55121904A (Direct) |
| AR (1) | AR220262A1 (Direct) |
| AU (1) | AU529647B2 (Direct) |
| BR (1) | BR8001031A (Direct) |
| CA (1) | CA1152292A (Direct) |
| DE (1) | DE3060836D1 (Direct) |
| FI (1) | FI65763C (Direct) |
| FR (1) | FR2450783A1 (Direct) |
| HK (1) | HK58183A (Direct) |
| IL (1) | IL59423A (Direct) |
| MX (1) | MX5990E (Direct) |
| MY (1) | MY8500048A (Direct) |
| OA (1) | OA06569A (Direct) |
| PH (1) | PH14413A (Direct) |
| TR (1) | TR22513A (Direct) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5607698A (en) * | 1988-08-04 | 1997-03-04 | Ciba-Geigy Corporation | Method of preserving ophthalmic solution and compositions therefor |
| US5132099A (en) * | 1990-12-27 | 1992-07-21 | Mitsubishi Gas Chemical Company, Inc. | Method for producing hydrogen peroxide |
| EP4065561B1 (de) | 2019-11-29 | 2023-08-16 | Evonik Operations GmbH | Verfahren zur herstellung salzarmer wässriger lösungen von 4-ammonium-alkylpiperidin-1-yloxylsalzen zum einsatz in ladungsspeichereinheiten |
| WO2021104684A1 (de) | 2019-11-29 | 2021-06-03 | Evonik Operations Gmbh | Verbessertes verfahren zur herstellung wässriger lösungen von 4-ammonium-alkylpiperidin-1-yloxylsalzen zum einsatz in ladungsspeichereinheiten |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB744633A (en) * | 1952-06-06 | 1956-02-08 | Dow Chemical Co | N-alkyl-(or-aralkyl-) substituted alkylene polyamine methylene phosphonic acid compounds |
| GB1392284A (en) * | 1971-03-30 | 1975-04-30 | Unilever Ltd | Stabilisation of active oxygen releasing compounds |
| US4057440A (en) * | 1976-01-29 | 1977-11-08 | Pennwalt Corporation | Scale reducer for zinc phosphating solutions |
| GB1563521A (en) * | 1977-01-10 | 1980-03-26 | Monsanto Europe Sa | Organophosphorus scale inhibitor compositions and their use in aqueous alkaline cleaning solutions |
-
1979
- 1979-03-05 FR FR7905600A patent/FR2450783A1/fr active Granted
-
1980
- 1980-02-13 PH PH23640A patent/PH14413A/en unknown
- 1980-02-14 AU AU55557/80A patent/AU529647B2/en not_active Ceased
- 1980-02-18 AR AR279995A patent/AR220262A1/es active
- 1980-02-18 MX MX808649U patent/MX5990E/es unknown
- 1980-02-19 IL IL59423A patent/IL59423A/xx unknown
- 1980-02-21 BR BR8001031A patent/BR8001031A/pt unknown
- 1980-02-25 EP EP80400259A patent/EP0015818B1/fr not_active Expired
- 1980-02-25 DE DE8080400259T patent/DE3060836D1/de not_active Expired
- 1980-02-28 CA CA000346645A patent/CA1152292A/fr not_active Expired
- 1980-03-03 JP JP2535880A patent/JPS55121904A/ja active Pending
- 1980-03-04 FI FI800660A patent/FI65763C/fi not_active IP Right Cessation
- 1980-03-05 OA OA57042A patent/OA06569A/xx unknown
- 1980-03-05 TR TR1690/80A patent/TR22513A/xx unknown
-
1983
- 1983-11-24 HK HK581/83A patent/HK58183A/xx unknown
-
1985
- 1985-12-30 MY MY48/85A patent/MY8500048A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BR8001031A (pt) | 1980-10-29 |
| DE3060836D1 (en) | 1982-11-04 |
| MY8500048A (en) | 1985-12-31 |
| EP0015818B1 (fr) | 1982-09-15 |
| OA06569A (fr) | 1981-08-31 |
| FI65763B (fi) | 1984-03-30 |
| AR220262A1 (es) | 1980-10-15 |
| MX5990E (es) | 1984-09-17 |
| TR22513A (tr) | 1987-09-16 |
| FI800660A7 (fi) | 1980-09-06 |
| AU5555780A (en) | 1980-09-11 |
| FR2450783A1 (fr) | 1980-10-03 |
| PH14413A (en) | 1981-07-09 |
| CA1152292A (fr) | 1983-08-23 |
| IL59423A0 (en) | 1980-05-30 |
| AU529647B2 (en) | 1983-06-16 |
| HK58183A (en) | 1983-12-02 |
| EP0015818A1 (fr) | 1980-09-17 |
| IL59423A (en) | 1983-02-23 |
| FR2450783B1 (Direct) | 1982-10-15 |
| JPS55121904A (en) | 1980-09-19 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: OXYSYNTHESE |