DE1221845B - Diesel fuels - Google Patents
Diesel fuelsInfo
- Publication number
- DE1221845B DE1221845B DEJ21845A DEJ0021845A DE1221845B DE 1221845 B DE1221845 B DE 1221845B DE J21845 A DEJ21845 A DE J21845A DE J0021845 A DEJ0021845 A DE J0021845A DE 1221845 B DE1221845 B DE 1221845B
- Authority
- DE
- Germany
- Prior art keywords
- wear
- ooc
- fuels
- carbon atoms
- diesel fuels
- Prior art date
- 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
Links
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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/08—Use of additives to fuels or fires for particular purposes for improving lubricity; for reducing wear
-
- 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/192—Macromolecular compounds
- C10L1/198—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
-
- 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/192—Macromolecular compounds
- C10L1/198—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
- C10L1/1983—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyesters
-
- 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/192—Macromolecular compounds
- C10L1/198—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
- C10L1/1985—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyethers, e.g. di- polygylcols and derivatives; ethers - esters
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Combustion & Propulsion (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Fuel-Injection Apparatus (AREA)
Description
DEUTSCHESGERMAN
PATENTAMTPATENT OFFICE
AUSLEGESCHRIFTEDITORIAL
Int. CL:Int. CL:
Nummer:
Aktenzeichen:
Anmeldetag:
Auslegetag:Number:
File number:
Registration date:
Display day:
ClOlClOl
Deutsche KL: 46 a6 - 7German KL: 46 a6 - 7
J21845IVd/46a6
29. Mai 1962
28. Juli 1966J21845IVd / 46a6
May 29, 1962
July 28, 1966
Die Abnutzung der Einspritzvorrichtungen von Dieselmotoren, die mit leichteren Kraftstoffen als Gasöl betrieben werden, wird immer problematischer. Dies gilt besonders für Motoren, die mit verschiedenen Kraftstoffen betrieben werden können, wie sie besonders in Entwicklungsländern benutzt werden, in denen die mit Benzin betriebenen Tourenwagen wenig verbreitet sind und in denen daher ein Überangebot an leichten Erdölfraktionen besteht.The wear and tear on the injectors of diesel engines using lighter fuels than Gas oil is becoming more and more problematic. This is especially true for engines that use different Fuels can be operated as they are used in developing countries in particular in which petrol-powered touring cars are not very common and in which there is therefore an oversupply consists of light petroleum fractions.
Es ist daher die Aufgabe der Erfindung, Dieselkraftstoff^ mit verminderter Abnutzung der Einspritzvorrichtungen aus leichten Brennstoffen oder Erdölfraktionen zu schaffen.It is therefore the object of the invention to provide diesel fuel ^ with reduced wear and tear on injectors from light fuels or petroleum fractions to accomplish.
Dies geschieht durch Zusatz von 0,01 bis 5 Gewichtsprozent eines Polyesters der Formel:This is done by adding 0.01 to 5 percent by weight of a polyester of the formula:
R1 - (- OOC - A - COO - B -)„ - OOC - A - COOR8 R 1 - (- OOC - A - COO - B -) "- OOC - A - COOR 8
in der A ein zweiwertiger aliphatischer, aromatischer oder naphthenischer Rest ist, der eventuell substituiert sein kann und 4 bis 20 Kohlenstoffatome enthält, B einen Alkylenrest mit 2 bis 20 Kohlenstoffatomen sowie R1 und R2 Alkylreste bedeuten und η eine ganze Zahl mindestens gleich 1 ist.in which A is a divalent aliphatic, aromatic or naphthenic radical which may be substituted and contains 4 to 20 carbon atoms, B is an alkylene radical with 2 to 20 carbon atoms and R 1 and R 2 are alkyl radicals and η is an integer at least equal to 1 .
Die folgenden Verbindungen können dazu verwendet werden:The following connections can be used for this:
DieselkraftstoffeDiesel fuels
Anmelder:Applicant:
Institut Frangais du Petrole des CarburantsInstitut Frangais du Petrole des Carburants
et Lubrifiants,et Lubrifiants,
Rueil-Malmaison, Seine-et-Oise (Frankreich)Rueil-Malmaison, Seine-et-Oise (France)
Vertreter:Representative:
Dr.-Ing. G. Riebling, Patentanwalt,Dr.-Ing. G. Riebling, patent attorney,
Lindau (Bodensee), Rennerle 10Lindau (Lake Constance), Rennerle 10
Als Erfinder benannt:Named as inventor:
Jean Larbre, Colombes, Seine;Jean Larbre, Colombes, Seine;
Louis Pons,Louis Pons,
Rueil-Malmaison, Seine-et-Oise (Frankreich)Rueil-Malmaison, Seine-et-Oise (France)
Beanspruchte Priorität:Claimed priority:
Frankreich vom 31. Mai 1961 (863 694)France of May 31, 1961 (863 694)
Mischpolyadipat aus Propylenglykol und Isodecanol, Mixed polyadipate from propylene glycol and isodecanol,
Mischpolyadipat aus Propylenglykol und Isododecanol, Mixed polyadipate from propylene glycol and isododecanol,
Mischpolysebacat aus Äthylenglykol und Isohexanol. Mixed polysebacate from ethylene glycol and isohexanol.
Diese Verbindungen werden vorteilhaft in einer Konzentration von 0,01 bis 5 und vorzugsweise von 0,05 bis 0,5 Gewichtsprozent verwendet.These compounds are advantageously used at a concentration of from 0.01 to 5, and preferably from 0.05 to 0.5 weight percent used.
Die Auflösung dieser Produkte kann durch ihre vorherige Verdünnung mittels aromatischer Kohlenwasserstoffe oder Kohlenwasserstoffgemischem'.teinem hohen Gehalt an Aromaten erleichtert ν erdsa.These products can be dissolved by diluting them beforehand using aromatic hydrocarbons or hydrocarbon mixtures with a high aromatic content, ν erdsa facilitates.
Die erfindungsgemäß verwendeten Polyester haben eine ihre Anwendungszeit überdauernde Wirkung, so daß die mechanischen Einspritzvorrichtungen mehrere Stunden ohne nennenswerte Abnützung verwendet werden können.The polyesters used in the present invention have an effect lasting their time of use, so that the mechanical injectors can be used for several hours without significant wear and tear.
Es sei noch bemerkt, daß bei Verwendung gleicher Mengen der üblichen Schmiermittel gleicher Viskosität keine vergleichbaren Ergebnisse erzielt werden können. Die Hauptmerkmale der Kraftstoffe und ihre Oktanzahlen werden durch den Zusatz dieser Produkte nicht verändert, und der Motor wird nicht verschmutzt.It should also be noted that when using the same amounts of the usual lubricants the same viscosity no comparable results can be achieved. The main characteristics of fuels and their octane numbers are not changed by the addition of these products, and the engine is not contaminated.
Einem auf einen Druck von 170 kg/cm2 eingestellten Einspritzer, dessen Nadel vorher in einem Kernreaktor bestrahlt wurde, wird mittels einer Kolbenpumpe Kraftstoff zugeführt. Die sich aus der Abnutzung der Nadel ergebenden Metallteilchen werden von dem Kraftstoff weggespült und sammeln sich auf einem Glasfrittefilter, durch das der Kraftstoff austritt. Aus der Messung der Radioaktivität des Filters schließt man auf die Menge der sich aus der Abnutzung der Nadel ergebenden Teilchen durch Vergleiche mit Teilen des gleichen Metalls, die der gleichen Bestrahlung unterworfen wurden und deren Gewicht bekannt ist.An injector set to a pressure of 170 kg / cm 2 , the needle of which was previously irradiated in a nuclear reactor, is supplied with fuel by means of a piston pump. The metal particles resulting from the wear of the needle are washed away by the fuel and collect on a glass frit filter through which the fuel exits. By measuring the radioactivity of the filter, the amount of particles resulting from the wear of the needle is inferred by comparing it with parts of the same metal which have been subjected to the same irradiation and whose weight is known.
Der verwendete Kraftstoff ist ein nicht äthyliertes Benzin mit einer Oktanzahl von 87, in dem ein Mischpolyadipat aus Propylenglykol und rohem Isodecanol aufgelöst wurde. Die letztgenannte Verbindung wurde durch Reaktion von 14,5 Mol Adipinsäure mit 12,9 Mol Propylenglykol und 5 Mol Isodecanol erhalten.The fuel used is a non-ethylated gasoline with an octane rating of 87, in which a mixed polyadipate was dissolved from propylene glycol and crude isodecanol. The latter connection was made obtained by reacting 14.5 moles of adipic acid with 12.9 moles of propylene glycol and 5 moles of isodecanol.
Auf Grund der erzielten Ergebnisse wurde die folgende Tabelle aufgestellt, die in Abhängigkeit von der in Gewichtsprozent ausgedrückten Konzentration des Zusatzes die entsprechenden Abnutzungswerte des Einspritzers bei 250C sowie bei 700C wiedergibt, wobei unter Abnutzung das Verhältnis der beobachteten Abnutzung zu der in Abwesenheit eines Zusatzmittels entstehenden Abnutzung steht, ausgedrückt durch die entsprechenden Gewichtsverluste.On the basis of the results obtained, the following table was drawn up which, depending on the concentration of the additive expressed in percent by weight, shows the corresponding wear values of the injector at 25 ° C. and at 70 ° C., with wear being the ratio of the wear observed to that in the absence wear resulting from an additive, expressed by the corresponding weight loss.
609 607/181609 607/181
25° C VOI
25 ° C
Will man bei der Verwendung von Rizinusöl eine Verringerung der Abnutzung um 50% bei 25° C erzielen, so muß man eine ungefähr 50mal stärkere Konzentration, also eine l%ige verwenden.If it is desired for the use of castor oil, a reduction of wear by 50% at 25 ° C achieved, an about 50 times higher concentration, ie use a l% strength must be e.
Claims (1)
USA.-Patentschrift Nr. 2 844 448.Considered publications:
U.S. Patent No. 2,844,448.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR863694A FR1317217A (en) | 1961-05-31 | 1961-05-31 | Method of reducing wear in injection engines and fuel compositions for these engines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1221845B true DE1221845B (en) | 1966-07-28 |
Family
ID=8756419
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEJ21845A Pending DE1221845B (en) | 1961-05-31 | 1962-05-29 | Diesel fuels |
Country Status (4)
| Country | Link |
|---|---|
| DE (1) | DE1221845B (en) |
| FR (1) | FR1317217A (en) |
| GB (1) | GB949707A (en) |
| OA (1) | OA01604A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3916365A1 (en) * | 1989-05-19 | 1990-11-22 | Basf Ag | FUEL COMPOSITIONS CONTAINING ALKOXYLATION PRODUCTS |
| US5466267A (en) * | 1992-09-17 | 1995-11-14 | Mobil Oil Corporation | Oligomeric/polymeric multifunctional additives to improve the low-temperature properties of distillate fuels |
| US5538521A (en) * | 1993-12-23 | 1996-07-23 | Chevron Chemical Company | Fuel compositions containing polyalkyl and poly(oxyalkylene)aromatic esters |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2844448A (en) * | 1955-12-23 | 1958-07-22 | Texas Co | Fuels containing a deposit-control additive |
-
1961
- 1961-05-31 FR FR863694A patent/FR1317217A/en not_active Expired
-
1962
- 1962-05-29 DE DEJ21845A patent/DE1221845B/en active Pending
- 1962-05-31 GB GB21101/62A patent/GB949707A/en not_active Expired
-
1964
- 1964-12-31 OA OA51637A patent/OA01604A/en unknown
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2844448A (en) * | 1955-12-23 | 1958-07-22 | Texas Co | Fuels containing a deposit-control additive |
Also Published As
| Publication number | Publication date |
|---|---|
| OA01604A (en) | 1969-09-20 |
| GB949707A (en) | 1964-02-19 |
| FR1317217A (en) | 1963-02-08 |
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