CH498925A - Verfahren zur Verbesserung der die Vereisung verhindernden Eigenschaften eines Motortreibstoffs, nach dem Verfahren erhaltener Motortreibstoff und Motortreibstoffzusatz zur Durchführung dieses Verfahrens - Google Patents
Verfahren zur Verbesserung der die Vereisung verhindernden Eigenschaften eines Motortreibstoffs, nach dem Verfahren erhaltener Motortreibstoff und Motortreibstoffzusatz zur Durchführung dieses VerfahrensInfo
- Publication number
- CH498925A CH498925A CH669966A CH669966A CH498925A CH 498925 A CH498925 A CH 498925A CH 669966 A CH669966 A CH 669966A CH 669966 A CH669966 A CH 669966A CH 498925 A CH498925 A CH 498925A
- Authority
- CH
- Switzerland
- Prior art keywords
- alkyl
- salt
- acidic
- dependent
- salts
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 55
- 239000000446 fuel Substances 0.000 title claims description 40
- 230000008569 process Effects 0.000 title claims description 15
- 239000002816 fuel additive Substances 0.000 title claims description 10
- 150000003839 salts Chemical class 0.000 claims description 112
- 239000000203 mixture Substances 0.000 claims description 96
- 230000002378 acidificating effect Effects 0.000 claims description 69
- 229910019142 PO4 Inorganic materials 0.000 claims description 62
- 235000021317 phosphate Nutrition 0.000 claims description 62
- 125000000217 alkyl group Chemical group 0.000 claims description 58
- -1 alkyl phosphate Chemical compound 0.000 claims description 49
- 239000010452 phosphate Substances 0.000 claims description 45
- 230000001419 dependent effect Effects 0.000 claims description 42
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 41
- 239000002253 acid Substances 0.000 claims description 31
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 28
- 239000000654 additive Substances 0.000 claims description 26
- 125000004432 carbon atom Chemical group C* 0.000 claims description 20
- 150000002148 esters Chemical class 0.000 claims description 20
- 230000000996 additive effect Effects 0.000 claims description 17
- 150000004985 diamines Chemical class 0.000 claims description 17
- XEJNLUBEFCNORG-UHFFFAOYSA-N ditridecyl hydrogen phosphate Chemical class CCCCCCCCCCCCCOP(O)(=O)OCCCCCCCCCCCCC XEJNLUBEFCNORG-UHFFFAOYSA-N 0.000 claims description 17
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 14
- 235000011180 diphosphates Nutrition 0.000 claims description 12
- 238000002156 mixing Methods 0.000 claims description 12
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 10
- 230000002195 synergetic effect Effects 0.000 claims description 10
- LTHNHFOGQMKPOV-UHFFFAOYSA-N 2-ethylhexan-1-amine Chemical compound CCCCC(CC)CN LTHNHFOGQMKPOV-UHFFFAOYSA-N 0.000 claims description 9
- 239000004480 active ingredient Substances 0.000 claims description 8
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 claims description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 5
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 claims description 4
- WJZUIWBZDGBLKK-UHFFFAOYSA-N dipentyl hydrogen phosphate Chemical compound CCCCCOP(O)(=O)OCCCCC WJZUIWBZDGBLKK-UHFFFAOYSA-N 0.000 claims description 4
- TUFJPPAQOXUHRI-KTKRTIGZSA-N n'-[(z)-octadec-9-enyl]propane-1,3-diamine Chemical compound CCCCCCCC\C=C/CCCCCCCCNCCCN TUFJPPAQOXUHRI-KTKRTIGZSA-N 0.000 claims description 4
- 239000003760 tallow Substances 0.000 claims description 4
- 150000003973 alkyl amines Chemical class 0.000 claims description 3
- 150000008043 acidic salts Chemical class 0.000 claims description 2
- 238000011109 contamination Methods 0.000 claims description 2
- HTDKEJXHILZNPP-UHFFFAOYSA-N dioctyl hydrogen phosphate Chemical class CCCCCCCCOP(O)(=O)OCCCCCCCC HTDKEJXHILZNPP-UHFFFAOYSA-N 0.000 claims description 2
- 238000010348 incorporation Methods 0.000 claims description 2
- VSRBKQFNFZQRBM-UHFFFAOYSA-N tuaminoheptane Chemical compound CCCCCC(C)N VSRBKQFNFZQRBM-UHFFFAOYSA-N 0.000 claims 1
- 150000001412 amines Chemical class 0.000 description 10
- 150000004712 monophosphates Chemical class 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 7
- 238000005259 measurement Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000003599 detergent Substances 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000011833 salt mixture Substances 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- JYFHYPJRHGVZDY-UHFFFAOYSA-N Dibutyl phosphate Chemical compound CCCCOP(O)(=O)OCCCC JYFHYPJRHGVZDY-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 229920005372 Plexiglas® Polymers 0.000 description 2
- 150000001335 aliphatic alkanes Chemical group 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- SNAMIIGIIUQQSP-UHFFFAOYSA-N bis(6-methylheptyl) hydrogen phosphate Chemical class CC(C)CCCCCOP(O)(=O)OCCCCCC(C)C SNAMIIGIIUQQSP-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- WBJBEMDHFMUSAY-UHFFFAOYSA-N dibutyl phosphono phosphate Chemical compound CCCCOP(=O)(OP(O)(O)=O)OCCCC WBJBEMDHFMUSAY-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- FACIWBZCZQRQBU-UHFFFAOYSA-N dipentadecyl hydrogen phosphate Chemical compound CCCCCCCCCCCCCCCOP(O)(=O)OCCCCCCCCCCCCCCC FACIWBZCZQRQBU-UHFFFAOYSA-N 0.000 description 2
- ZKSXQLOUZSQHCK-UHFFFAOYSA-N dipentadecyl phosphono phosphate Chemical compound CCCCCCCCCCCCCCCOP(=O)(OCCCCCCCCCCCCCCC)OP(=O)(O)O ZKSXQLOUZSQHCK-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000007710 freezing Methods 0.000 description 2
- 230000008014 freezing Effects 0.000 description 2
- 238000002309 gasification Methods 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 2
- VFFCVKZHJFIUBM-UHFFFAOYSA-N pentyl trihydrogen diphosphate Chemical compound CCCCCO[P@](O)(=O)OP(O)(O)=O VFFCVKZHJFIUBM-UHFFFAOYSA-N 0.000 description 2
- SRADUCBCRVYVPI-UHFFFAOYSA-N phosphoric acid tridecanoic acid Chemical class P(=O)(O)(O)O.C(CCCCCCCCCCCC)(=O)O.C(CCCCCCCCCCCC)(=O)O SRADUCBCRVYVPI-UHFFFAOYSA-N 0.000 description 2
- 125000004437 phosphorous atom Chemical group 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- LOULAQZMQREUDL-UHFFFAOYSA-N CCCCCCCCCCCCCCCOP(O)(OP(O)(O)=O)=O Chemical compound CCCCCCCCCCCCCCCOP(O)(OP(O)(O)=O)=O LOULAQZMQREUDL-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000005700 Putrescine Substances 0.000 description 1
- 150000001447 alkali salts Chemical group 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000001204 arachidyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- CREXVNNSNOKDHW-UHFFFAOYSA-N azaniumylideneazanide Chemical group N[N] CREXVNNSNOKDHW-UHFFFAOYSA-N 0.000 description 1
- 238000013142 basic testing Methods 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- BNMJSBUIDQYHIN-UHFFFAOYSA-N butyl dihydrogen phosphate Chemical compound CCCCOP(O)(O)=O BNMJSBUIDQYHIN-UHFFFAOYSA-N 0.000 description 1
- VERZAHGVEDNDSE-UHFFFAOYSA-N butyl phosphono hydrogen phosphate Chemical compound CCCCOP(O)(=O)OP(O)(O)=O VERZAHGVEDNDSE-UHFFFAOYSA-N 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000007596 consolidation process Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- DIOQZVSQGTUSAI-NJFSPNSNSA-N decane Chemical compound CCCCCCCCC[14CH3] DIOQZVSQGTUSAI-NJFSPNSNSA-N 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000001236 detergent effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000033001 locomotion Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- HIEAVKFYHNFZNR-UHFFFAOYSA-N pentadecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCCCCOP(O)(O)=O HIEAVKFYHNFZNR-UHFFFAOYSA-N 0.000 description 1
- NVTPMUHPCAUGCB-UHFFFAOYSA-N pentyl dihydrogen phosphate Chemical compound CCCCCOP(O)(O)=O NVTPMUHPCAUGCB-UHFFFAOYSA-N 0.000 description 1
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical class NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 description 1
- 125000005936 piperidyl group Chemical group 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000029305 taxis Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/26—Organic compounds containing phosphorus
- C10L1/2633—Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond)
- C10L1/2658—Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond) amine salts
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45416765A | 1965-05-07 | 1965-05-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH498925A true CH498925A (de) | 1970-11-15 |
Family
ID=23803576
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH669966A CH498925A (de) | 1965-05-07 | 1966-05-09 | Verfahren zur Verbesserung der die Vereisung verhindernden Eigenschaften eines Motortreibstoffs, nach dem Verfahren erhaltener Motortreibstoff und Motortreibstoffzusatz zur Durchführung dieses Verfahrens |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US3425815A (da) |
| BE (1) | BE680542A (da) |
| CH (1) | CH498925A (da) |
| DE (1) | DE1545508B1 (da) |
| DK (1) | DK117118B (da) |
| ES (1) | ES326413A1 (da) |
| GB (1) | GB1139186A (da) |
| NL (1) | NL6606121A (da) |
| SE (1) | SE339771B (da) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005033253A1 (de) * | 2003-10-07 | 2005-04-14 | Swiss E-Technic Ag | Schwefelarmes öl, verfahren zur senkung der aggressivität eines solchen öls |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3639110A (en) * | 1968-12-02 | 1972-02-01 | Marathon Oil Co | Detergent gasoline composition |
| GB9401710D0 (en) * | 1994-01-29 | 1994-03-23 | Castrol Ltd | Anti-wear additives and their use |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU33880A1 (da) * | 1954-10-04 | |||
| US2863904A (en) * | 1955-05-09 | 1958-12-09 | Gulf Oil Corp | Amine salts of di oxo-octyl orthophosphates |
| NL100963C (da) * | 1955-11-23 | |||
| US3063820A (en) * | 1959-05-18 | 1962-11-13 | Universal Oil Prod Co | Stabilization of hydrocarbons |
| US3130018A (en) * | 1962-09-12 | 1964-04-21 | Du Pont | Anti-stalling composition |
-
1965
- 1965-05-07 US US454167A patent/US3425815A/en not_active Expired - Lifetime
-
1966
- 1966-05-03 GB GB19364/66A patent/GB1139186A/en not_active Expired
- 1966-05-05 DK DK233766AA patent/DK117118B/da unknown
- 1966-05-05 NL NL6606121A patent/NL6606121A/xx unknown
- 1966-05-05 BE BE680542D patent/BE680542A/xx unknown
- 1966-05-06 SE SE06275/66A patent/SE339771B/xx unknown
- 1966-05-06 ES ES0326413A patent/ES326413A1/es not_active Expired
- 1966-05-06 DE DE19661545508 patent/DE1545508B1/de active Pending
- 1966-05-09 CH CH669966A patent/CH498925A/de not_active IP Right Cessation
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005033253A1 (de) * | 2003-10-07 | 2005-04-14 | Swiss E-Technic Ag | Schwefelarmes öl, verfahren zur senkung der aggressivität eines solchen öls |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1545508B1 (de) | 1971-01-14 |
| BE680542A (da) | 1966-10-17 |
| GB1139186A (en) | 1969-01-08 |
| ES326413A1 (es) | 1967-07-01 |
| NL6606121A (da) | 1966-11-08 |
| DK117118B (da) | 1970-03-16 |
| US3425815A (en) | 1969-02-04 |
| SE339771B (da) | 1971-10-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1570870C3 (de) | Aminacylierungsprodukte von kohlenwasserstoffsubstituierter Bernsteinsäure und deren Verwendung | |
| DE1271287B (de) | Die Wasserabweisung, Rostverhuetung und Verhinderung des Eisansatzes bewirkender Zusatz in Treibstoffen, hydrophoben Traegermitteln und UEberzugsmitteln | |
| EP0289785A1 (de) | Verfahren zur Verhinderung oder Verminderung von Ablagerungen in Gemischaufbereitungssystemen von Motoren | |
| DE1545502C3 (de) | Neue Salze von sauren Alkylphosphaten mit Alkanolamine^ deren Herstellung und deren Verwendung als Kraftstoffadditive | |
| DE3852668T3 (de) | Brennstoffzusammensetzung mit einem Zusatz zur Verminderung des Rückschlags des Ventilsitzes. | |
| DE2112321C2 (de) | Amingemische enthaltende Benzinzubereitung | |
| CH498925A (de) | Verfahren zur Verbesserung der die Vereisung verhindernden Eigenschaften eines Motortreibstoffs, nach dem Verfahren erhaltener Motortreibstoff und Motortreibstoffzusatz zur Durchführung dieses Verfahrens | |
| DE1042808B (de) | Schmieroel | |
| DE1235062B (de) | Stabilisieren von Destillatbrennstoffen | |
| DE2138569A1 (de) | Treibstoff- und Schmiermittelzubereitungen | |
| EP0282845A1 (de) | Kraftstoffe, enthaltend geringe Mengen Alkoxylate und Polycarbonsäureimide | |
| DE2531469C3 (de) | Verwendung von w -N.N.N'.N'tetrasubstituierten Aminoalkansäureamiden, w -N,N,N',N'tetrasubstituierte Aminobuttersäure-amide und Verfahren zu deren Herstellung | |
| DE1125716B (de) | Zusatzmittel fuer Motorbenzine | |
| DE1545508C (de) | Antivereisungsadditiv fur Motorkraft stoffe | |
| DE1957487C (de) | Vergaser Kraftstoff | |
| DE950339C (de) | Motortreibstoffgemisch | |
| DE1082453B (de) | Treibstoffe fuer Duesentriebwerke | |
| DE2610798A1 (de) | Treibstoffe fuer ottomotoren | |
| DE941217C (de) | Stabilisiertes Heizoel | |
| DE1108004B (de) | Motorenleichtbenzine | |
| AT214034B (de) | Verfahren zur Behandlung von Motorbenzinen | |
| DE1094038B (de) | Motorenbenzin | |
| DE1031576B (de) | Treibstoff fuer Ottomotoren | |
| DE2417788A1 (de) | Verwendung von amiden von cyclischen polycarbonsaeuren als zusatz zu treibstoffen | |
| DE1250676B (de) | Kraftstoffe vom Benzinsiedebereich fur Verbrennungskraftmaschinen |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |