DE2407158B2 - PETROL DISTILLATE FUELS OR FUEL - Google Patents
PETROL DISTILLATE FUELS OR FUELInfo
- Publication number
- DE2407158B2 DE2407158B2 DE19742407158 DE2407158A DE2407158B2 DE 2407158 B2 DE2407158 B2 DE 2407158B2 DE 19742407158 DE19742407158 DE 19742407158 DE 2407158 A DE2407158 A DE 2407158A DE 2407158 B2 DE2407158 B2 DE 2407158B2
- Authority
- DE
- Germany
- Prior art keywords
- ethylene
- oil
- oils
- percent
- weight
- 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, 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
- C10L1/192—Macromolecular compounds
- C10L1/195—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
-
- 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
- C10L1/192—Macromolecular compounds
- C10L1/195—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C10L1/196—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof
- C10L1/1963—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof mono-carboxylic
-
- 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
- C10L1/192—Macromolecular compounds
- C10L1/195—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C10L1/197—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and an acyloxy group of a saturated carboxylic or carbonic acid
- C10L1/1973—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and an acyloxy group of a saturated carboxylic or carbonic acid mono-carboxylic
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Lubricants (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
gedanke zugrunde, Erdöldestillat-Brenn-bzw.-Treib- säure-2-äthylhexylester im Gewichtsverhältnis 1 :1 stoffe zur Verfugung zu stellen, die durch die erfin- als 60%ige Lösung eine Viskosität von 900 bis 950 cst. dungsgemäßen Zusätze größere Mengen an ausschei- Die entsprechenden Lösungen der einzelnen Polymeridungsfähigen Paraffinen enthalten können, ohne daß sate haben Viskositäten von 2000 bis 1500 cst. Die der Anwendungsbereich bei tiefen Temperaturen ein- S Lösungen der Gemische lassen sich somit wesentlich geschränkt wird. Somit ist es möglich, ohne Anwen- leichter pumpen und handhaben, dung von Spaltverfahren durch gewöhnliche Destil- Der Gegenstand der Erfindung sei an folgendenThe idea is based on petroleum distillate fuel or propellant 2-ethylhexyl ester in a weight ratio of 1: 1 To provide substances that have a viscosity of 900 to 950 cst due to the inven- tive 60% solution. Appropriate additives larger amounts of separable The corresponding solutions of the individual Polymeridungsbaren Paraffins can contain without sate have viscosities from 2000 to 1500 cst. the The range of application at low temperatures can thus be significantly reduced is restricted. This makes it possible to pump and handle more easily without the need for a user dung of cleavage processes by ordinary distillation The object of the invention is based on the following
lation aus Rohölen einen größeren Anteil an Mittel- Beispielen veranschaulicht destillaten zu gewinnen.lation from crude oils illustrates a larger proportion of medium examples to win distillates.
Geeignete Erdöldestillat-Brenn- bzw. -Treibstoffe io BeispiellSuitable petroleum distillate fuels or fuels io example
sind solche, die durch Destillation aus Rohölen verschiedener Provenienz erzeugt werden und als Gasöle, Einem Heizöl EL aus Rohöl saudiarabischer ProDieselöle oder leichtes Heizöl bekannt sind. Sie haben venienz mit einem Siedebereich von 220 bis 3500C «inen Siedebereich von 120 bis 4000C. Geeignete und einem CFPP-Wrt (DIN 51428) von -163C wird Destillate haben z. B. Stockpunkte von —5 bis — 300C. 15 ein Mischpolymerisat aus Äthylen und Äthyl-2-hexyl-are those that are produced by distillation from crude oils of various origins and are known as gas oils, a heating oil EL from crude oil from Saudi Arabian ProDiesel oils or light heating oil. You have venience with a boiling range from 220 to 350 0 C «in a boiling range from 120 to 400 0 C. Suitable and a CFPP-Wrt (DIN 51428) of -16 3 C will have distillates z. B. Pour points from -5 to -30 0 C. 15 a copolymer of ethylene and ethyl-2-hexyl-
Die Erdökiestillat-Brenn- bzw. -Treibstoffe ent- acrylat mit 55 Molprozent 2-Äthylhexylacrylat (1) mit
halten öllösliche Mischpolymerisate aus Äthylen und einem Molekulargewicht von 3850 sowie ein Misch-Fettsäurevinylestern
mit einem Molekulargewicht von polymerisat aus Äthylen und Vinylacetat mit 45 MoI-500
bis 8000 sowie öllösliche Mischpolymerisate aus prozent Vinylacetat (II) und einem Molekulargewicht
Äthylen und Acrylsäurealkylestern mit einem Mole- ao von 3600 in den in nachfolgender Tabelle angegebenen
kulargewicht von 500 bis 10 000. Die beiden Misch- Msngen und Verhältnissen zugesetzt und die dort aufpolymerisate
sind zusammen in Mengen von 0.001 bis gezeigten Ergebnisse erhalten. 0,1 Gewichtsprozent enthalten. Vorzugsweise beträgt
deren Gehalt von 0,005 bis 0,02 Gewichtsprozent.
Mischpolymerisate aus Äthylen und Fettsäurevinyl- as Tabelle I
estern und Mischpolymerisate aus Äthylen und Acrylsäurealkylestern werden im Gewichtsverhältnis von
1:10 bis 10:1, insbesondere im Gewichtsverhältnis
von 1: 3 bis 3 :1, angewandt.The petroleum distillate fuel or propellants entacrylate with 55 mol percent 2-ethylhexyl acrylate (1) with hold oil-soluble copolymers of ethylene and a molecular weight of 3850 as well as a mixed fatty acid vinyl ester with a molecular weight of polymer from ethylene and vinyl acetate with 45 mol 500 to 8000 as well as oil-soluble copolymers of percent vinyl acetate (II) and a molecular weight of ethylene and acrylic acid alkyl esters with a Mole- ao of 3600 in the kular weight of 500 to 10 000 given in the table below. The two mixed quantities and ratios added and the polymerized there are obtained together in amounts from 0.001 to shown results. 0.1 percent by weight. Preferably is
their content from 0.005 to 0.02 percent by weight.
Copolymers of ethylene and fatty acid vinyl esters as Table I and copolymers of ethylene and acrylic acid alkyl esters are in a weight ratio of
1:10 to 10: 1, especially in a weight ratio
from 1: 3 to 3: 1, applied.
Bevorzugt wendet man öllösliche Mischpolymerisate 3° aus Äthylen und Vinylestern mit Fettsäuren von 1 bis 8 Kohlenstoffatomen, insbesondere 2 bis 4 Kohlenstoffatomen, an. Der Gehalt an Fettsäurevinylestern beträgt vorteilhaft 40 bis 60 Molprozent. Der bevorzugte Bereich des Molekulargewichts beträgt 2000 bis 35 8000. Besonders technische Bedeutung haben Mischpolymerisate aus Äthylen und Vinylicetat, die 40 bis 60 Molprozent Vinylacetat enthalten und ein Molekulargewicht von 3000 bis 5000 haben.It is preferred to use oil-soluble copolymers 3 ° of ethylene and vinyl esters with fatty acids from 1 to 8 carbon atoms, especially 2 to 4 carbon atoms. The content of fatty acid vinyl esters is advantageously 40 to 60 mol percent. The preferred range of molecular weight is 2,000 to 35 8000. Copolymers of ethylene and vinyl acetate, the 40 to Contain 60 mole percent vinyl acetate and have a molecular weight of 3000 to 5000.
Bevorzugte öllösliche Mischpolymerisate aus Äthy- 40
len und Acrylsäurealkylestern sind solche, die Acrylester
mit Alkanolen von 2 bis 20, insbesondere 4 bis 12
Kohlenstoffatomen enthalten. In den bevorzugten
Mischpolymerisaten sind Acrylsäurealkylester in Men- Man verwendet das im Beispiel 1 beschriebene Heizgen
von 40 bis 60 Molprozent enthalten. Vorteilhaft 45 öl, setzt jedoch die dort aufgeführten Polymerisate I
haben die Polymerisate ein Molekulargewicht von und II einzeln in den in nachfolgender Tabelle an-3000
bis 5000. Besondere technische Bedeutung hat gegebenen Mengen zu und erhält die daraus ersichtein
Polymerisat aus Äthylen und 45 bis 60 Molprozent lichen CFPP-Werte.
Acrylsäure-2-äthylhexylester mit einem Molekulargewicht
von 3000 bis 5000 erlangt. 50Preferred oil-soluble copolymers made from Ethy- 40
len and acrylic acid alkyl esters are those which acrylic esters with alkanols of 2 to 20, in particular 4 to 12
Contain carbon atoms. In the preferred
Copolymers are acrylic acid alkyl esters in men- Man uses the heating agent described in Example 1 and contains 40 to 60 mol percent. Advantageously 45 oil, but if the polymers I listed there are used, the polymers have a molecular weight of and II individually in the following table from -3000 to 5000. The amounts given are of particular technical importance and are derived from a polymer of ethylene and 45 to 60 Mole percent CFPP values. Acrylic acid-2-ethylhexyl ester with a molecular weight of 3000 to 5000 obtained. 50
Die angegebenen Molekulargewichte werden be- Tabelle II stimmt nach der osmometrischen Methode. The indicated molecular weights are determined by the osmometric method. Table II.
Geeignete Öllösliche Mischpolymerisate aus Äthylen Menge Polymerisate CFPP-WertSuitable oil-soluble copolymers of ethylene Amount of polymers CFPP value
und Fettsäurevinylestern bzw. Acrylsäurealkylestern Gewichts- Gewichtsverhältnisand fatty acid vinyl esters or acrylic acid alkyl esters by weight to weight ratio
erhält man z. B. nach Verfahren, wie sie aus den 55 Prozent you get z. B. according to procedures as they are from the 55 percent
deutschen Patentschriften 11 62 630 und 12 50 188 bekannt sind. 0,01German patents 11 62 630 and 12 50 188 are known. 0.01
Die Mischungen der Polymerisate werden in der 0,01
Regel als 40- bis 60gewichtsprozentige Lösungen in 0,025
Kohlenwasserstoffen, wie Schwerbenzin, Schwerplat- 60 0,025
format, gehandhabt und den Erdöldestillaten in den
genannten Mengen zugesetzt. Die Mischungen aus den
genannten Polymerisaten in Lösung ist insofern vorteilhaft zu handhaben, als sie gegenüber gleich- Ein Dieselöl nordafrikanischer Provenienz mit
gewichtsprozentigen Lösungen der einzelnen Polymeren 65 einem CFPP-Wert von —9°C wird wie im Beispiell
eine verminderte Viskosität haben. Zum Beispiel hat mit den dort beschriebenen Polymerisaten I und II
eine Mischung aus einem Mischpolymerisat aus versetzt. Die näheren Ergebnisse sind aus nachÄthylen
und Vinylacetat sowie Äthylen und Acryl- folgender Tabelle zu entnehmen.The mixtures of the polymers are in the 0.01
Usually as 40 to 60 percent by weight solutions in 0.025
Hydrocarbons, such as heavy gasoline, heavy plateau 60 0.025
format, handled and the petroleum distillates in the
mentioned amounts added. The mixtures of the
The above-mentioned polymers in solution are advantageous insofar as they have a reduced viscosity compared to the same as in the example. For example, the polymers I and II described there have been mixed with a mixture of a copolymer. The more detailed results can be found in the table below for ethylene and vinyl acetate as well as ethylene and acrylic.
Gewichts
prozentlot
Weight
percent
GewichtsverhältnisPolymers
Weight ratio
20 TeUe II80 parts I.
20 TeUe II
30 Teile II70 parts I.
30 parts II
40 Teile II60 parts I.
40 parts II
30 Teile II70 parts I.
30 parts II
Menge
Gewichtsprozentlot
Weight percent
Polymerisat GewichtsverhältnisPolymer weight ratio
0,010.01
0,010.01
70 Teile I 30 Teile II70 parts I 30 parts II
60 Teile I 40 TeUe II60 parts I 40 TeU II
CFPP-WertCFPP value
-13°C-13 ° C
-200C-20 0 C
in den in nachfolgender Tabelle angegebenen Mengen zu und erhält die dort beschriebenen CFPP-Werte.in the amounts specified in the table below and receives the CFPP values described there.
Mengelot
GewichtsprozentWeight percent
PolymerisatPolymer
CFPP-WertCFPP value
0,01
0,010.01
0.01
I III II
-100C -1O0C-10 0 C -1O 0 C
VergleichsbeispielComparative example
Aus den Vergleichsversuchen ist ersichtlich, daß Destillate, die ein Gemisch aus den Polymerisaten I und II enthalten, einen wesentlich weiteren Anwen-Man verwendet das im Beispiel 2 beschriebene dungsbereich bei tiefen Temperaturen haben als Dieselöl, setzt jedoch die Polymerisate 1 und II einzeln 15 solche, die die Polymerisate einzeln enthalten.From the comparative experiments it can be seen that distillates which are a mixture of the polymers I and II contain a much wider application than the application range described in Example 2 at low temperatures Diesel oil, however, uses polymers 1 and II individually 15 those which contain the polymers individually.
Claims (1)
genannten Stockpunkt solcher Mitteldestillate zuAttempts have already been made to add 45 to the weight of 500 to 10,000
called pour point of such middle distillates
tiefen Temperaturen zu beseitigen und eine uneinge- Die so verbesserten Erdöldestillat-Brenn- bzw.reduce the disadvantageous phenomena in the weight ratio 1:10 to 10: 1.
The so improved petroleum distillate fuel or
die genannten Polymerisate den Nachteil, daß die Der Erfindung liegt der allgemeine Erfindungs-It is also already known that oil-soluble copolymers from cleavage processes make it possible to increase the proportion of ethylene with fatty acid vinyl esters to the pour point of middle distillates. However, this requires the use of degradation (cf. DT-PS 1162 630). significant investment. With the increasing use of copolymers of ethylene and acrylic acid in crude oil, efforts are being made, and esters have already been used in a higher proportion for the same purpose with ordinary distillation (cf. DT-PS 12 50 188). To gain the effectiveness of middle distillates. Up to now, however, this has not been possible for these polymers, in particular in the case of applications, since extensive distillation of small amounts has not yet proven to be technically sufficient as a considerable enrichment in excretable quantities. In addition, paraffins have entered the middle distillates,
the said polymers have the disadvantage that the invention is the general invention
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19742407158 DE2407158B2 (en) | 1974-02-15 | 1974-02-15 | PETROL DISTILLATE FUELS OR FUEL |
NL7501194A NL7501194A (en) | 1974-02-15 | 1975-01-31 | PROCESS FOR PREPARING PETROLEUM DISTILLED FUEL AND / OR ENGINE FUELS. |
SE7501570A SE390975B (en) | 1974-02-15 | 1975-02-12 | MINERAL OIL DISTILLATE FUEL OR FUEL WITH A BOILING INTERVAL OF APPROXIMATELY 120-40072? |
FR7504331A FR2261333A1 (en) | 1974-02-15 | 1975-02-12 | Pour point improvers for middle distillate oils - contg. ethylene-vinyl ester and ethylene-acrylate ester copolymers |
FI750373A FI750373A (en) | 1974-02-15 | 1975-02-12 | |
BE153348A BE825523A (en) | 1974-02-15 | 1975-02-14 | FUELS AND FUELS BASED ON OIL DISTILLATES |
AT112375A AT337866B (en) | 1974-02-15 | 1975-02-14 | EARTH DISTILLATE FUELS OR FUEL |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19742407158 DE2407158B2 (en) | 1974-02-15 | 1974-02-15 | PETROL DISTILLATE FUELS OR FUEL |
Publications (2)
Publication Number | Publication Date |
---|---|
DE2407158A1 DE2407158A1 (en) | 1975-08-21 |
DE2407158B2 true DE2407158B2 (en) | 1976-01-15 |
Family
ID=5907433
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19742407158 Pending DE2407158B2 (en) | 1974-02-15 | 1974-02-15 | PETROL DISTILLATE FUELS OR FUEL |
Country Status (7)
Country | Link |
---|---|
AT (1) | AT337866B (en) |
BE (1) | BE825523A (en) |
DE (1) | DE2407158B2 (en) |
FI (1) | FI750373A (en) |
FR (1) | FR2261333A1 (en) |
NL (1) | NL7501194A (en) |
SE (1) | SE390975B (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4058371A (en) * | 1976-05-25 | 1977-11-15 | Exxon Research & Engineering Co. | Polymer combinations useful in distillate hydrocarbon oils to improve cold flow properties |
JPS5840391A (en) * | 1981-09-03 | 1983-03-09 | Sumitomo Chem Co Ltd | Improvement in low-temperature fluidity of fuel oil |
DE3725059A1 (en) * | 1987-07-29 | 1989-02-09 | Roehm Gmbh | POLYMER FLOW IMPROVERS FOR MEDIUM DISTILLATES |
US20230138313A1 (en) * | 2021-10-29 | 2023-05-04 | Ecolab Usa Inc. | Blends of ethylene vinyl acetate copolymer and an acrylate-containing copolymer as pour point depressants |
-
1974
- 1974-02-15 DE DE19742407158 patent/DE2407158B2/en active Pending
-
1975
- 1975-01-31 NL NL7501194A patent/NL7501194A/en unknown
- 1975-02-12 SE SE7501570A patent/SE390975B/en unknown
- 1975-02-12 FI FI750373A patent/FI750373A/fi not_active Application Discontinuation
- 1975-02-12 FR FR7504331A patent/FR2261333A1/en not_active Withdrawn
- 1975-02-14 BE BE153348A patent/BE825523A/en unknown
- 1975-02-14 AT AT112375A patent/AT337866B/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
BE825523A (en) | 1975-08-14 |
SE390975B (en) | 1977-01-31 |
DE2407158A1 (en) | 1975-08-21 |
FI750373A (en) | 1975-08-16 |
NL7501194A (en) | 1975-08-19 |
SE7501570L (en) | 1975-08-18 |
FR2261333A1 (en) | 1975-09-12 |
ATA112375A (en) | 1976-11-15 |
AT337866B (en) | 1977-07-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0398101B1 (en) | Reaction products of aminoalkylene-polycarboxylic acids with secondary amines and crude oil middle distillates containing them | |
DE1645785C3 (en) | Fuel oil mixture containing waxy residues with a reduced pour point | |
DE3137233C2 (en) | ||
DE1645873A1 (en) | Preparations containing hydrocarbons | |
DE1794416A1 (en) | OIL PREPARATION WITH IMPROVED FLOW AND SET POINT PROPERTIES | |
EP0254284A1 (en) | Process to improve the flowability of mineral oils and mineral oil distillates | |
EP0405270B1 (en) | Process to improve mineral oil and mineral oil distillate flowability | |
DE2331041A1 (en) | HEATING OIL FORMULATION | |
DE1645798B1 (en) | Use of a terpolymer as a pour point depressor for hydrocarbon fuel oils | |
DE1271456B (en) | Fuel oils | |
DE2407158B2 (en) | PETROL DISTILLATE FUELS OR FUEL | |
DD236940A5 (en) | ADDITIVE CONCENTRATE FOR INTEGRATION IN PETROLEUM DISTILLATE FUELS | |
EP0045342A1 (en) | Fuel composition with particular fluidity at low temperatures | |
DE2130816A1 (en) | Low-sulfur, deep-stocking fuel oil mixture and process for its production | |
DE1279267B (en) | Stabilization and increase of the electrical conductivity of liquid hydrocarbons or their mixtures | |
DE325883C (en) | Process to make viscous oils easy-flowing | |
DE3923249A1 (en) | MINERAL OIL WITH IMPROVED FLOW BEHAVIOR | |
DE754401C (en) | Process for lowering the pour point of oils | |
DE705540C (en) | Heating oil | |
DE1137261B (en) | Improvement of the filter point of diesel fuels and heating oils | |
DE1470595C (en) | Solvent extraction | |
DE651771C (en) | Process to improve the ignitability of diesel oils | |
DE2620840C2 (en) | ||
DD144066A1 (en) | NAVY DIESEL OIL WITH IMPROVED PUMPABILITY | |
DE1545481C (en) | Use of a gasoline fuel for direct injection into the combustion chamber of gasoline engines |