DE1133060B - Erhoehung der Leitfaehigkeit fluessiger Kohlenwasserstoffgemische - Google Patents

Erhoehung der Leitfaehigkeit fluessiger Kohlenwasserstoffgemische

Info

Publication number: DE1133060B
Authority: DE; Germany
Prior art keywords: metal; salt; use according; gram atom; conductivity
Prior art date: 1957-10-23
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

DEN15763A

Other languages

German (de)

English (en)

Inventor

Thurston Skei

James Edward Douglas

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Bataafsche Petroleum Maatschappij NV

Original Assignee

Bataafsche Petroleum Maatschappij NV

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1957-10-23

Filing date

1958-10-23

Publication date

1962-07-12

1958-10-23 Application filed by Bataafsche Petroleum Maatschappij NV filed Critical Bataafsche Petroleum Maatschappij NV

1962-07-12 Publication of DE1133060B publication Critical patent/DE1133060B/de

Status Pending legal-status Critical Current

Links

229930195733 hydrocarbon Natural products 0.000 title claims description 31
150000002430 hydrocarbons Chemical class 0.000 title claims description 31
239000007788 liquid Substances 0.000 title claims description 27
239000004215 Carbon black (E152) Substances 0.000 title claims description 23
239000000203 mixture Substances 0.000 title claims description 15
229910052751 metal Inorganic materials 0.000 claims description 46
239000002184 metal Substances 0.000 claims description 46
239000000446 fuel Substances 0.000 claims description 40
150000003839 salts Chemical class 0.000 claims description 39
125000004429 atom Chemical group 0.000 claims description 30
239000006078 metal deactivator Substances 0.000 claims description 21
150000001844 chromium Chemical class 0.000 claims description 17
239000011651 chromium Substances 0.000 claims description 9
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 8
239000002253 acid Substances 0.000 claims description 7
229910052804 chromium Inorganic materials 0.000 claims description 7
150000001875 compounds Chemical class 0.000 claims description 7
238000009835 boiling Methods 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 6
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 3
239000005977 Ethylene Substances 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
125000002723 alicyclic group Chemical group 0.000 claims description 2
125000001931 aliphatic group Chemical group 0.000 claims description 2
150000001447 alkali salts Chemical class 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
239000003209 petroleum derivative Substances 0.000 claims description 2
150000003254 radicals Chemical class 0.000 claims description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical class OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims 2
RURPJGZXBHYNEM-UHFFFAOYSA-N 2-[2-[(2-hydroxyphenyl)methylideneamino]propyliminomethyl]phenol Chemical compound C=1C=CC=C(O)C=1C=NC(C)CN=CC1=CC=CC=C1O RURPJGZXBHYNEM-UHFFFAOYSA-N 0.000 claims 1
230000007935 neutral effect Effects 0.000 claims 1
239000000654 additive Substances 0.000 description 22
229910052757 nitrogen Inorganic materials 0.000 description 12
230000003647 oxidation Effects 0.000 description 11
238000007254 oxidation reaction Methods 0.000 description 11
-1 aromatic carboxylic acids Chemical class 0.000 description 10
230000000996 additive effect Effects 0.000 description 6
230000000694 effects Effects 0.000 description 6
239000011575 calcium Substances 0.000 description 5
150000002739 metals Chemical class 0.000 description 5
159000000007 calcium salts Chemical class 0.000 description 4
238000001704 evaporation Methods 0.000 description 4
230000008020 evaporation Effects 0.000 description 4
238000012360 testing method Methods 0.000 description 4
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
229910052791 calcium Inorganic materials 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
238000002845 discoloration Methods 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
150000003460 sulfonic acids Chemical class 0.000 description 3
OXLXSOPFNVKUMU-UHFFFAOYSA-N 1,4-dioctoxy-1,4-dioxobutane-2-sulfonic acid Chemical compound CCCCCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCCCCC OXLXSOPFNVKUMU-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
239000010941 cobalt Substances 0.000 description 2
229910017052 cobalt Inorganic materials 0.000 description 2
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
230000005611 electricity Effects 0.000 description 2
CJMZLCRLBNZJQR-UHFFFAOYSA-N ethyl 2-amino-4-(4-fluorophenyl)thiophene-3-carboxylate Chemical compound CCOC(=O)C1=C(N)SC=C1C1=CC=C(F)C=C1 CJMZLCRLBNZJQR-UHFFFAOYSA-N 0.000 description 2
238000011835 investigation Methods 0.000 description 2
229910021645 metal ion Inorganic materials 0.000 description 2
238000011160 research Methods 0.000 description 2
230000003068 static effect Effects 0.000 description 2
229910052720 vanadium Inorganic materials 0.000 description 2
LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 2
HXISMZRZHNLOHG-UHFFFAOYSA-N 2-hydroxy-3,4-di(propan-2-yl)benzoic acid Chemical compound CC(C)C1=CC=C(C(O)=O)C(O)=C1C(C)C HXISMZRZHNLOHG-UHFFFAOYSA-N 0.000 description 1
WCKMDEHRHUNVEQ-UHFFFAOYSA-N 4-[1-(4-oxopentan-2-ylideneamino)ethylimino]pentan-2-one Chemical compound C(C(=O)C)C(C)=NC(C)N=C(C)CC(=O)C WCKMDEHRHUNVEQ-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
JGLMVXWAHNTPRF-CMDGGOBGSA-N CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O Chemical compound CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O JGLMVXWAHNTPRF-CMDGGOBGSA-N 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
230000002411 adverse Effects 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
239000002585 base Substances 0.000 description 1
150000001555 benzenes Chemical class 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
150000001868 cobalt Chemical class 0.000 description 1
239000000470 constituent Substances 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
KWABLUYIOFEZOY-UHFFFAOYSA-N dioctyl butanedioate Chemical class CCCCCCCCOC(=O)CCC(=O)OCCCCCCCC KWABLUYIOFEZOY-UHFFFAOYSA-N 0.000 description 1
238000004821 distillation Methods 0.000 description 1
229960000878 docusate sodium Drugs 0.000 description 1
238000007786 electrostatic charging Methods 0.000 description 1
238000005421 electrostatic potential Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000004880 explosion Methods 0.000 description 1
239000002360 explosive Substances 0.000 description 1
239000012530 fluid Substances 0.000 description 1
238000007710 freezing Methods 0.000 description 1
230000008014 freezing Effects 0.000 description 1
230000005484 gravity Effects 0.000 description 1
150000002505 iron Chemical class 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
230000007257 malfunction Effects 0.000 description 1
150000002696 manganese Chemical class 0.000 description 1
239000000463 material Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
238000000034 method Methods 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
230000008520 organization Effects 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
239000001294 propane Substances 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
150000003870 salicylic acids Chemical class 0.000 description 1
APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
239000004071 soot Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
238000003419 tautomerization reaction Methods 0.000 description 1
CMWCOKOTCLFJOP-UHFFFAOYSA-N titanium(3+) Chemical class [Ti+3] CMWCOKOTCLFJOP-UHFFFAOYSA-N 0.000 description 1
150000003681 vanadium Chemical class 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
- H01B1/12—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
- 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
- C10L1/18—Organic compounds containing oxygen
- C10L1/188—Carboxylic acids; metal salts thereof
- 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
- C10L1/22—Organic compounds containing nitrogen
- C10L1/228—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen double bond, e.g. guanidines, hydrazones, semicarbazones, imines; containing at least one carbon-to-nitrogen triple bond, e.g. nitriles
- C10L1/2283—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen double bond, e.g. guanidines, hydrazones, semicarbazones, imines; containing at least one carbon-to-nitrogen triple bond, e.g. nitriles containing one or more carbon to nitrogen double bonds, e.g. guanidine, hydrazone, semi-carbazone, azomethine
- 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
- C10L1/24—Organic compounds containing sulfur, selenium and/or tellurium
- C10L1/2431—Organic compounds containing sulfur, selenium and/or tellurium sulfur bond to oxygen, e.g. sulfones, sulfoxides
- C10L1/2437—Sulfonic acids; Derivatives thereof, e.g. sulfonamides, sulfosuccinic acid esters

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)
Physics & Mathematics (AREA)
Spectroscopy & Molecular Physics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Liquid Carbonaceous Fuels (AREA)

DEN15763A 1957-10-23 1958-10-23 Erhoehung der Leitfaehigkeit fluessiger Kohlenwasserstoffgemische Pending DE1133060B (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US861794XA	1957-10-23	1957-10-23

Publications (1)

Publication Number	Publication Date
DE1133060B true DE1133060B (de)	1962-07-12

Family

ID=22196814

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DEN15763A Pending DE1133060B (de)	1957-10-23	1958-10-23	Erhoehung der Leitfaehigkeit fluessiger Kohlenwasserstoffgemische

Country Status (4)

Country	Link
BE (1)	BE572324A (uk)
DE (1)	DE1133060B (uk)
FR (1)	FR1216340A (uk)
GB (1)	GB861794A (uk)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US7332627B2 (en) *	2001-06-12	2008-02-19	Lucent Technologies Inc.	Compositions comprising a solvated metal

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1566106A (en)	1976-03-17	1980-04-30	Nat Res Dev	Additives for aviation and similar fuels
GB9907058D0 (en) *	1999-03-26	1999-05-19	Infineum Uk Ltd	Fuel oil compositions
US8211190B2 (en)	1999-03-26	2012-07-03	Infineum International Limited	Fuel oil compositions

Citations (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR820975A (fr) *	1936-07-21	1937-11-24		Perfectionnements aux combustibles liquides
US2144654A (en) *	1936-09-14	1939-01-24	Leo Corp	Method of increasing solubility of metal salts of beta carboxy compounds in motor fuels
US2181121A (en) *	1937-12-29	1939-11-28	Du Pont	Stabilization of organic substances
FR965315A (uk) *		1950-09-08
GB676204A (en) *	1949-01-04	1952-07-23	Leo Corp	Improvements in or relating to the combustion of heating fuel oils
FR1070581A (fr) *	1952-11-13	1954-07-29	Nat Aluminate Corp	Procédé pour la réduction de la formation et du dépot de carbone dans la combustion des huiles combustibles et produits en résultant
GB770278A (en) *	1954-04-30	1957-03-20	Exxon Research Engineering Co	Fuel composition

0
- BE BE572324D patent/BE572324A/xx unknown
1958
- 1958-10-23 GB GB33942/58A patent/GB861794A/en not_active Expired
- 1958-10-23 DE DEN15763A patent/DE1133060B/de active Pending
- 1958-10-23 FR FR777345A patent/FR1216340A/fr not_active Expired

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR965315A (uk) *		1950-09-08
FR820975A (fr) *	1936-07-21	1937-11-24		Perfectionnements aux combustibles liquides
US2144654A (en) *	1936-09-14	1939-01-24	Leo Corp	Method of increasing solubility of metal salts of beta carboxy compounds in motor fuels
US2181121A (en) *	1937-12-29	1939-11-28	Du Pont	Stabilization of organic substances
GB676204A (en) *	1949-01-04	1952-07-23	Leo Corp	Improvements in or relating to the combustion of heating fuel oils
FR1070581A (fr) *	1952-11-13	1954-07-29	Nat Aluminate Corp	Procédé pour la réduction de la formation et du dépot de carbone dans la combustion des huiles combustibles et produits en résultant
GB770278A (en) *	1954-04-30	1957-03-20	Exxon Research Engineering Co	Fuel composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US7332627B2 (en) *	2001-06-12	2008-02-19	Lucent Technologies Inc.	Compositions comprising a solvated metal

Also Published As

Publication number	Publication date
FR1216340A (fr)	1960-04-25
BE572324A (uk)
GB861794A (en)	1961-02-22

Publication	Publication Date	Title
DE69517735T2 (de)	2001-03-01	Verfahren und Zusammensetzungen zur Strahltriebwerksverschmutzungsniederschlagsbildungverminderung
EP0078249B1 (de)	1987-10-28	Zusatz mit verbrennungsfördernder und russhemmender Wirkung zu Heizölen, Dieselkraftstoffen und sonstigen flüssigen Brenn- und Treibstoffen sowie flüssige Brenn- und Treibstoffe
DE894296C (de)	1953-10-22	Heizoelgemische
DE2944153C2 (de)	1983-04-14	Verfahren zur Verminderung der NO&darr;x&darr; - und/oder SO&darr;2&darr;-Emmission bei der Verbrennung von Brennstoffen
DE2614384A1 (de)	1977-10-13	Thermisches zersetzen von polychlorierten organischen verbindungen
DE1133060B (de)	1962-07-12	Erhoehung der Leitfaehigkeit fluessiger Kohlenwasserstoffgemische
EP0501097B1 (de)	1995-08-30	Treibstoff für Verbrennungsmotoren und Verwendung von Methylformiat
DE2539381A1 (de)	1976-03-18	Heterozyklische guanidin- alkylverbindung und ihre herstellung und verwendung als zusatzstoffe
DE3507613A1 (de)	1985-09-12	Nicht saeurehaltiger treibstoffzusatz fuer traegerkraftstoffe
DE2931260A1 (de)	1980-04-10	Hexakoordinierte uebergangsmetallverbindungen
DE935467C (de)	1955-11-17	Treibstoff fuer Verbrennungskraftmaschinen mit Fremdzuendung und Antiklopfmittelmischung
DE1057383B (de)	1959-05-14	Duesenkraftstoff
WO1995001411A1 (de)	1995-01-12	Treibstoff für verbrennungsmotoren und turbinen
DE1030953B (de)	1958-05-29	Brennstoffzusammensetzungen
US2912314A (en)	1959-11-10	Cracked fuel oils stabilized with amine salts of dithiocarbamic acids
DE2363848A1 (de)	1975-07-10	Verfahren zum betreiben von ottound rotationskolben-motoren
AT216654B (de)	1961-08-10	Leichtbenzin
DE4032845A1 (de)	1991-07-11	Hydrophile katalysatorloesung zur verbesserten verbrennung von kohlenstoff- und kohlenwasserstoffhaltigen stoffen
DE4421329C2 (de)	1998-02-26	Verwendung von trifunktionellen Alkoholen als Kraftstoffzusatz
DE1645781C (de)	1972-11-30	Verwendung von Mangan II Amin Koordinationskomplexen als Zusatz zu Brenn stoffen
DE1470630C (de)	1972-04-13	Kohlenwasserstoffgemische mit verbesserter Alterungsstabilität
DE1645874A1 (de)	1970-07-23	Verbesserte Duesentreibstoffe
DE870198C (de)	1953-03-12	Verfahren zur Stabilisierung von Benzin und Bleitetraaethyl enthaltenden Treibstoffen
DE1220196B (de)	1966-06-30	Treibstoffe fuer Ottomotoren
DE1099257B (de)	1961-02-09	Treibstoffe

DE1133060B - Erhoehung der Leitfaehigkeit fluessiger Kohlenwasserstoffgemische - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (1)

Publications (1)

Family

ID=22196814

Family Applications (1)

Country Status (4)

Cited By (1)

Families Citing this family (3)

Citations (7)

Patent Citations (7)

Cited By (1)

Also Published As

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