NO118221B - - Google Patents
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- Publication number
- NO118221B NO118221B NO163750A NO16375066A NO118221B NO 118221 B NO118221 B NO 118221B NO 163750 A NO163750 A NO 163750A NO 16375066 A NO16375066 A NO 16375066A NO 118221 B NO118221 B NO 118221B
- Authority
- NO
- Norway
- Prior art keywords
- accumulators
- accumulator
- plates
- charging
- electrolyte
- Prior art date
Links
- 239000003792 electrolyte Substances 0.000 claims description 22
- 239000000080 wetting agent Substances 0.000 claims description 15
- 239000002253 acid Substances 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 150000001768 cations Chemical class 0.000 claims description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 239000011149 active material Substances 0.000 claims 2
- 238000005323 electroforming Methods 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 16
- 239000000654 additive Substances 0.000 description 9
- 238000007599 discharging Methods 0.000 description 7
- 230000000996 additive effect Effects 0.000 description 6
- -1 alcohol sulphates Chemical class 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 230000005484 gravity Effects 0.000 description 5
- OJLOUXPPKZRTHK-UHFFFAOYSA-N dodecan-1-ol;sodium Chemical compound [Na].CCCCCCCCCCCCO OJLOUXPPKZRTHK-UHFFFAOYSA-N 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- OUUQCZGPVNCOIJ-UHFFFAOYSA-M Superoxide Chemical compound [O-][O] OUUQCZGPVNCOIJ-UHFFFAOYSA-M 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- KEQXNNJHMWSZHK-UHFFFAOYSA-L 1,3,2,4$l^{2}-dioxathiaplumbetane 2,2-dioxide Chemical compound [Pb+2].[O-]S([O-])(=O)=O KEQXNNJHMWSZHK-UHFFFAOYSA-L 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003595 mist Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical group C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- RKIMETXDACNTIE-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,5,5,6,6-dodecafluorocyclohexane Chemical compound FC1(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C1(F)F RKIMETXDACNTIE-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical class OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- MEPUPEPDWBTIDP-UHFFFAOYSA-N calcium;ethane-1,2-diol Chemical compound [Ca].OCCO MEPUPEPDWBTIDP-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000002301 combined effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000000644 propagated effect Effects 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/88—Oxygen atoms
- C07D239/92—Oxygen atoms with hetero atoms directly attached to nitrogen atoms of the hetero ring
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Secondary Cells (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF0046616 | 1965-07-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO118221B true NO118221B (forum.php) | 1969-12-01 |
Family
ID=7101133
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO163750A NO118221B (forum.php) | 1965-07-16 | 1966-07-01 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US3481928A (forum.php) |
| AT (1) | AT266142B (forum.php) |
| BE (1) | BE684270A (forum.php) |
| BR (1) | BR6681324D0 (forum.php) |
| CH (1) | CH476022A (forum.php) |
| DE (1) | DE1545832A1 (forum.php) |
| DK (1) | DK118947B (forum.php) |
| ES (2) | ES329067A1 (forum.php) |
| FR (1) | FR5904M (forum.php) |
| GB (1) | GB1103155A (forum.php) |
| NL (1) | NL6609924A (forum.php) |
| NO (1) | NO118221B (forum.php) |
| SE (1) | SE325889B (forum.php) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4377408A (en) * | 1981-07-27 | 1983-03-22 | Rhone-Poulenc Agrochimie | Herbicidal derivatives of 5-phenoxy-4(3H)-quinazolinone-1-oxide |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1007331A (en) * | 1960-12-01 | 1965-10-13 | Fisons Pest Control Ltd | Quinazolin-3-oxides and benzo-1,2,3-triazine-3-oxides |
| US3162636A (en) * | 1963-01-23 | 1964-12-22 | S B Penick & Company | 1-alkyl-2-hetero-1, 2, 3, 4-tetrahydro-quinazoline-4-ones |
-
1965
- 1965-07-16 DE DE19651545832 patent/DE1545832A1/de active Pending
-
1966
- 1966-06-30 US US561761A patent/US3481928A/en not_active Expired - Lifetime
- 1966-07-01 NO NO163750A patent/NO118221B/no unknown
- 1966-07-08 DK DK356566AA patent/DK118947B/da unknown
- 1966-07-13 ES ES0329067A patent/ES329067A1/es not_active Expired
- 1966-07-13 CH CH1016366A patent/CH476022A/de not_active IP Right Cessation
- 1966-07-13 ES ES0329065A patent/ES329065A1/es not_active Expired
- 1966-07-14 SE SE09665/66A patent/SE325889B/xx unknown
- 1966-07-14 NL NL6609924A patent/NL6609924A/xx unknown
- 1966-07-14 AT AT677866A patent/AT266142B/de active
- 1966-07-15 GB GB31968/66A patent/GB1103155A/en not_active Expired
- 1966-07-15 BR BR181324/66A patent/BR6681324D0/pt unknown
- 1966-07-18 BE BE684270D patent/BE684270A/xx unknown
- 1966-10-14 FR FR80053A patent/FR5904M/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| CH476022A (de) | 1969-07-31 |
| FR5904M (forum.php) | 1968-03-25 |
| US3481928A (en) | 1969-12-02 |
| ES329065A1 (es) | 1967-08-16 |
| NL6609924A (forum.php) | 1967-01-17 |
| AT266142B (de) | 1968-11-11 |
| DK118947B (da) | 1970-10-26 |
| ES329067A1 (es) | 1967-08-16 |
| DE1545832A1 (de) | 1969-10-23 |
| BE684270A (forum.php) | 1967-01-18 |
| SE325889B (forum.php) | 1970-07-13 |
| BR6681324D0 (pt) | 1973-12-26 |
| GB1103155A (en) | 1968-02-14 |
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