NL8020472A - COPPER FUEL CATALYST. - Google Patents
COPPER FUEL CATALYST. Download PDFInfo
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- NL8020472A NL8020472A NL8020472A NL8020472A NL8020472A NL 8020472 A NL8020472 A NL 8020472A NL 8020472 A NL8020472 A NL 8020472A NL 8020472 A NL8020472 A NL 8020472A NL 8020472 A NL8020472 A NL 8020472A
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- isopropanol
- methanol
- toluene
- additive
- picric acid
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- 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
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- 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
- C10L1/12—Inorganic compounds
- C10L1/1208—Inorganic compounds elements
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- 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
- C10L1/12—Inorganic compounds
- C10L1/1233—Inorganic compounds oxygen containing compounds, e.g. oxides, hydroxides, acids and salts thereof
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- 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
- C10L1/12—Inorganic compounds
- C10L1/1275—Inorganic compounds sulfur, tellurium, selenium containing compounds
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- 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
- C10L1/16—Hydrocarbons
- C10L1/1608—Well defined compounds, e.g. hexane, benzene
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- 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
- C10L1/16—Hydrocarbons
- C10L1/1616—Hydrocarbons fractions, e.g. lubricants, solvents, naphta, bitumen, tars, terpentine
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- 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
- C10L1/182—Organic compounds containing oxygen containing hydroxy groups; Salts thereof
- C10L1/1822—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
- C10L1/1824—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
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- 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
- C10L1/185—Ethers; Acetals; Ketals; Aldehydes; Ketones
- C10L1/1857—Aldehydes; Ketones
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- 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
- C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
- C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
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- 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
- C10L1/23—Organic compounds containing nitrogen containing at least one nitrogen-to-oxygen bond, e.g. nitro-compounds, nitrates, nitrites
- C10L1/231—Organic compounds containing nitrogen containing at least one nitrogen-to-oxygen bond, e.g. nitro-compounds, nitrates, nitrites nitro compounds; nitrates; nitrites
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B3/00—Engines characterised by air compression and subsequent fuel addition
- F02B3/06—Engines characterised by air compression and subsequent fuel addition with compression ignition
Description
' - S 5935-1 PCT/Ned. elz/yh 802 04 72 P & c ' Koperkatalysator voor brandstoffen.S 5935-1 PCT / Ned. elz / yh 802 04 72 P & c 'Copper catalyst for fuels.
De onderhavige uitvinding verschaft een energie besparend brandstof-toevoegsel voor benzine- en dieselmotoren, meer in het bijzonder met inbegrip van toevoeging aan huisbrandolie en lichte industriële olie (no. 2 5 en no. 3) en residu- en bunkerbrandstoffen (no. 4, no. 5 en no. 6). Dit brandstoftoevoegsel bevat als aktieve bestanddelen een overwegende hoeveelheid picrinezuur en een minimale hoeveelheid cuprisulfaat (CuSO^Igeen H2°) : (I) Cuprisulfaat 0,01 - 0,03% 10 Picrinezuur 1 - 2 % 1 Methanol 35 - 50 % ; 1 Isopropanol 15 - 5 % ' Tolueen 43-48 %The present invention provides an energy-saving fuel additive for gasoline and diesel engines, more particularly including addition to domestic heating oil and light industrial oil (No. 2 and No. 3) and residual and bunker fuels (No. 4, No. 5 and No. 6). This fuel additive contains as active ingredients a predominant amount of picric acid and a minimal amount of cupric sulfate (CuSO 4 Igene H 2 °): (I) Cupric sulfate 0.01 - 0.03% 10 Picric acid 1 - 2% 1 Methanol 35 - 50%; 1 Isopropanol 15 - 5% Toluene 43 - 48%
Nitrobenzeen 0,6 - 1,0 % 15 Primeen 81R 0,5 - 1,0 %Nitrobenzene 0.6 - 1.0% 15 Primene 81R 0.5 - 1.0%
Bovendien kan men cuprosulfaat toepassen in plaats van cuprisulfaat, hoewel dit niet de voorkeur verdient. oIn addition, cuprous sulfate may be used in place of cupric sulfate, although this is not preferred. O
Het basisch toevoegsel heeft twee variaties, die eveneens onder de uitvinding vallen. Volgens één variatie wordt de tolueen vervangen door 20 een oplosmiddel verhouding van bijvoorbeeld ca. 10 gew.% methanol en 90 gew.% isopropanol.The basic additive has two variations, which are also covered by the invention. In one variation, the toluene is replaced with a solvent ratio of, for example, about 10 wt% methanol and 90 wt% isopropanol.
(II) Cuprisulfaat 0,01 - 0,03%(II) Cupric sulfate 0.01 - 0.03%
Picrinezuur 1 - 2 %Picric acid 1 - 2%
Methanol 35 - 50 % 25 Isopropanol 15 - 5 %Methanol 35 - 50% 25 Isopropanol 15 - 5%
Methanol/isopropanol 10/90 43 - 48 % | Nitrobenzeen 0,6 - 1,0 %Methanol / isopropanol 10/90 43 - 48% | Nitrobenzene 0.6 - 1.0%
Primeen 81R 0,5 - 1,0 % | | Het vervangingsmengsel van methanol en isopropanol kan gevarieerd |30 worden tot een verhouding 50/50. Het doel van de vervanging van tolueen j ^daardoor is een geringere toxiciteit.Primene 81R 0.5 - 1.0% | | The replacement mixture of methanol and isopropanol can be varied to a ratio of 50/50. The purpose of replacing toluene as a result is lower toxicity.
ii
Volgens het tweede alternatief wordt tolueen vervangen door ca. 10% J imethanol, 45% isopropanol en 45% keroseen. "fAccording to the second alternative, toluene is replaced by about 10% J imethanol, 45% isopropanol and 45% kerosene. "f
(III) Cuprisulfaat 0,01 - 0,0.3% f[ ^ ,v. f;h T(III) Cupric sulfate 0.01 - 0.0.3% f [^, v. f; h T
| | Methanol 35 — 50 % 1 ' ! Isopropanol 15 - 5 % I :::::.11:..| | Methanol 35 - 50% 1 '! Isopropanol 15 - 5% I :::::. 11: ..
! Methanol/isopropanol/ 43 - 48 % | keroseen 10/45/45 i 40 Nitrobenzeen 0,6 - 1,Ö'!‘% 8020472! Methanol / isopropanol / 43 - 48% | kerosene 10/45/45 i 40 Nitrobenzene 0.6 - 1, Ö '! "% 8020472
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Primeen 81R 0,5 - 1,0%Primene 81R 0.5 - 1.0%
Het als vervanging voor tolueen gebruikte mengsel van methanol/ isopropanol/keroseen kan gevarieerd worden tot ca. 25% methanol, 25% isopropanol en 50% keroseen. Dit alternatief, dat keroseen bevat, dient 5 'teivbeheersing van de kosten.The methanol / isopropanol / kerosene mixture used as a substitute for toluene can be varied to about 25% methanol, 25% isopropanol and 50% kerosene. This alternative, which contains kerosene, serves to control costs.
De verdere ontwikkelingen, die verband houden met de uitvinding, maar waarvoor hier geen rechten worden gevraagd, zijn als volgt.The further developments related to the invention, but for which no rights are claimed here, are as follows.
Een verder produkt, dat beoogt een hoog ontvlammingspunt in benzine te geven, bevat: 10 (IV) Groen basisch kopercarbonaat- hydroxide, C^CO^ (Off) ^ 1 - 3%A further product, which aims to give a high flash point in gasoline, contains: 10 (IV) Green basic copper carbonate hydroxide, C ^ CO ^ (Off) ^ 1 - 3%
Picrinezuur 1—- 2%Picric acid 1—- 2%
Methyl-isobutylketon (MIBK) 3 — 7% n.butanol 10 - 25% ,_ Keroseen 65 - 74% 15 ,Methyl isobutyl ketone (MIBK) 3 - 7% n.butanol 10 - 25%, Kerosene 65 - 74% 15,
Nitrobenzeen 0,04 — 0,1.2% jNitrobenzene 0.04 - 0.1.2% j
Primeen 81R 0,02 - 0,10% ' Verder is verwant aan de onderhavige samenstellingen een diesèlmengsel met hoog ontvlammingspunt, bevattende: ......Primene 81R 0.02-0.10% Further related to the present compositions is a high flash point diesel mixture containing: ......
| (V) Elementair ijzer 0,01 — 0,03%| (V) Iron Elemental 0.01 - 0.03%
Picrinezuur 1-2%Picric acid 1-2%
Methyl-isobutylketon (MIBK) 4 — 6%..Methyl Isobutyl Ketone (MIBK) 4 - 6%.
n.butanol 15 - 25% ! Keroseen 70 - 74% \ Nitrobenzeen 0,05 — 1%n.butanol 15 - 25%! Kerosene 70 - 74% \ Nitrobenzene 0.05 - 1%
Primeen 81R 0,05 - 1%Primene 81R 0.05 - 1%
Stand der techniekState of the art
Van primair belang ten opzichte van de bekende octrooiliteratuur zijn drie octrooien van Dr. Harry M.Webb, overgedragen aan XRG International, inc. Volgens deze groep octrooien, namelijk U.S. 4.099.930, U.S. 4.129.421 ; ! en U.S. 4.145.190, gebruikt men ferrosulfaat in kombinatie met picrinezuur, j terwijl water aanwezüg is in het oplosmiddelmilieu. De onderhavige toevoeg— ! seis zijn in meerderheid gebaseerd op cuprisulfaat in kombinatie met j | picrinezuur en bij afwezigheid van water. Een'ander octrooischrift is j L_ U.S. 1.669.181.Of primary importance compared to the known patent literature are three patents of Dr. Harry M. Webb, transferred to XRG International, inc. According to this group of patents, namely U.S. 4,099,930, U.S. 4,129,421; ! and U.S. 4,145,190, ferrous sulfate is used in combination with picric acid, while water is present in the solvent medium. The present add-on! majority are based on cupric sulfate in combination with j | picric acid and in the absence of water. Another patent is L. 1,669,181.
35 ; J Van primair belang bij de onderhavige aanvrage en uitvinding is de basissamenstelling, waarbij cuprisulfaat wordt toegepast in plaats van het : | ferrosulfaat uit de stand der techniek van Webb. Gevonden werd, dat het ; cinderhavige, koper bevattende mengsel aktiever is en meer vermogen aan de ¢07047235; J Of primary interest in the present application and invention is the base composition, using cupric sulfate in place of the: | prior art ferrous sulfate from Webb. It was found that it; The present copper-containing mixture is more active and more potent at 070472
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- 3 - brandstof geeft dan de eerder gebruikte ferro-samenstellingen. De bij voorkeur toegepaste componenten van toevoegsel I zijn:- 3 - fuel then gives the previously used ferrous compositions. The preferred components of additive I are:
Cuprisulfaat (geen water) 0,02%Cupric sulfate (no water) 0.02%
Picrinezuur 1,5 % 5 Methanol 35 %Picric acid 1.5% 5 Methanol 35%
Isopropanol 15 %Isopropanol 15%
Tolueen 48,3%Toluene 48.3%
Nitrobenzeen 0,8%Nitrobenzene 0.8%
Primeen 81R 0,5% 10 De voorkeurscomponenten van toevoegsel II zijn dezelfde als de voor keurscomponenten van toevoegsel I, maar het tolueen wordt vervangen door een combinatie van 10% methanol en 90% isopropanol.Primene 81R 0.5% 10 The preferred components of Additive II are the same as the preferred components of Additive I, but the toluene is replaced by a combination of 10% methanol and 90% isopropanol.
De voorkeurscomponenten van toevoegsel III zijn dezelfde als de voor-keurscomponenten van toevoegsel I, maar het tolueen wordt vervangen door 15 een kombinatie van 10% methanol, 45% isopropanol en 45% keroseen. Alle percentages zijn gewichtspercentages.The preferred components of Additive III are the same as the preferred components of Additive I, but the toluene is replaced with a combination of 10% methanol, 45% isopropanol and 45% kerosene. All percentages are weight percentages.
Verwante produkten, die onder de uitvinding vallen, zijn samenstellingen, die verband houden met benzine met een hoog ontvlammingspunt en waarin men de volgende voorkeurscomponenten toepast: 20 | Groen basisch kopercarbonaat- | hydroxide 2%Related products covered by the invention are compositions which are related to high flash point gasoline and which employ the following preferred components: 20 | Green basic copper carbonate | hydroxide 2%
Picrinezuur 11,5%Picric acid 11.5%
Methyl-isobutylketon (MIBK) 5% n.butanol 20% 25 Keroseen 71,3%Methyl Isobutyl Ketone (MIBK) 5% n.butanol 20% 25 Kerosene 71.3%
Nitrobenzeen 0,08%Nitrobenzene 0.08%
Primeen 81R 0,05% I In een andere samenstelling voor dieselolie met hoog ontvlammingspunt gebruikt men de volgende voorkeurscomponenten: ijQ Elementair ijzer 0,1% i Picrinezuur 1,5% | Methyl-isobutylketon (MIBK) 5% n.butanol 20% I Keroseen 73,2% 35 Nitrobenzeen 0,08% j | Primeen 81R 0,05%Primene 81R 0.05% I In another formulation for high flash point diesel oil, the following preferred components are used: ijQ Elemental Iron 0.1% i Picric Acid 1.5% | Methyl isobutyl ketone (MIBK) 5% n.butanol 20% I Kerosene 73.2% 35 Nitrobenzene 0.08% y | Primene 81R 0.05%
De bestanddelen i KoperSulfaat. Het kopersulfaat, dat geschikt is volgens de uitvinding,; ' is cuprisulfaat, bij voorkeur de gedehydrateerde variëteit CuSO^. geen H^O.The constituents i Copper Sulphate. The copper sulfate suitable according to the invention; is cupric sulfate, preferably the dehydrated variety CuSO4. no H ^ O.
80204728020472
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Proeven hebben aangetoond, dat de synergistische katalytische werkzaamheid van deze verbinding die van het eerder gebruikte ijzer of ferrosulfaat in aanmerkelijke mate overtreft.Tests have shown that the synergistic catalytic activity of this compound far exceeds that of the previously used iron or ferrous sulfate.
Picrinezuur. Dit trinitrofenol werkt synergistisch met het cuprosulfaat 5 om de aktieve component van de uitvinding te geven.Picric acid. This trinitrophenol acts synergistically with the cuprous sulfate 5 to give the active component of the invention.
De aromatische oplosmiddelen. Bij voorkeur past men als aromatisch oplosmiddel tolueen toe. Onder de mogelijke alkylbenzenen verdienen tolueen, ortho-, meta-r en paraxyleen de voorkeur en zijn de mesitylênen i bruikbaar. Bij sommige van de onderhavige toepassingen wordt het tolueen 10 vervangen door andere, minder toxische oplosmiddelen.The aromatic solvents. Toluene is preferably used as the aromatic solvent. Among the possible alkylbenzenes, toluene, ortho, meta-r and paraxylene are preferred and the mesityles are useful. In some of the present applications, the toluene 10 is replaced by other less toxic solvents.
De alcoholische oplosmiddelen. Onder de lage alkanolen, die volgens de uitvinding geschikt zijn, verdienen methanol en isopropanol de voorkeur, hoewel men iedere lage alkanol met 1-6 koolstofatomen een rechte of vertakte keten kan toepassen. Van verder belang is normaal butanol, dat toegepast 15;wordt in het preparaat, dat bestemd is om een hoog ontvlammingspunt te :geven.The alcoholic solvents. Among the lower alkanols which are suitable according to the invention, methanol and isopropanol are preferred, although any lower alkanol of 1-6 carbon atoms can be straight or branched chain. Of further interest is normal butanol which is used in the composition intended to give a high flash point.
Nitrobenzeen. Deze verbinding wordt toegepast als een verder oplosmiddel. Hij is mengbaar met alkanolen en is een bijzonder goed organisch oplosmiddel voor het picrinezuur.Nitrobenzene. This compound is used as a further solvent. It is miscible with alkanols and is a particularly good organic solvent for the picric acid.
20 Primeen. Primenen zijn tertiaire alkylaminen, die een kruising zijn van primaire alifatische aminen met de algemene formule R^ (R^)(R^JCNH^f waarin de aminogroep gebonden is aan een tertiair koolstofatoom. De volgens de uitvinding toegepaste aminen zijn Primeen 81R en Primeen JM-T, waarbij de 81R de voorkeur verdient. Deze aminen zijn anti-oxidantia en stabi-25 liseermiddelen voor brandstofoliën en straalbrandstoffen.20 Primene. Primenes are tertiary alkylamines, which are a cross of primary aliphatic amines of the general formula R ^ (R ^) (R ^ JCNH ^ f in which the amino group is bonded to a tertiary carbon atom. The amines used according to the invention are Primene 81R and Primene JM-T with the 81R being preferred These amines are antioxidants and stabilizers for fuel oils and jet fuels.
Voorbeeld 1 Vóór het uitvoeren van proeven werden de katalytische omzetters uit alle voertuigen verwijderd. Het proefprogramma begon met een basislijn federale beproevingsmethode (Federal Test Procedure(FTP) en met de proef 30 betreffende brandstofeconomie op de autoweg (Highway Fuel Economy Test, (HFET). Vervolgens werden 'duplicaat FTP en HFET proeven uitgevoerd om te verifiëren of de gegevens reproduceerbaar waren. Hierna werd het eerste toevoegsel.gekombineerd met de commerciële, geen lood bevattende brand-! stof in een hoeveelheid van 28,35 g (1 ounce) toevoegsel per 45,42 1 35 (12 gallon) brandstof. Er werd een FTP/HFET proefreeks uitgevoerd en direkt daarna volgden duplicaatproeven.Example 1 Before carrying out tests, the catalytic converters were removed from all vehicles. The pilot program began with a baseline federal test method (Federal Test Procedure (FTP) and Highway Fuel Economy Test, (HFET) test 30. Then duplicate FTP and HFET tests were performed to verify that the data The first additive was then combined with the commercial unleaded fuel in the amount of 28.35 g (1 ounce) additive per 45.42 l 35 (12 gallons) of fuel. / HFET test series performed and duplicate tests followed immediately thereafter.
De katalytische omzetters werden op hun plaats gelast alvorens de volgende proefserie begon. Er werden basislijn FTP en HFET-proeven uitgevoerd en duplicaat basislijn proeven volgden. Hetzelfde toevoegsel,dafcoyoor 8020472The catalytic converters were welded in place before the next run. Baseline FTP and HFET tests were performed and duplicate baseline tests followed. The same additive, dafcoyoor 8020472
ÜK022LCÜK022LC
- 5 - beproeving zonder katalytische omzetters was gebruikt, werd daarna toegevoegd in dezelfde 12:1 verhouding. Er werden FTP/HFET-proeven met toevoegsel uitgevoerd op alle voertuigen met direkt daarna duplicaat proeven.Test without catalytic converters was used, then added in the same 12: 1 ratio. FTP / HFET additive tests were performed on all vehicles with duplicate tests immediately thereafter.
De katalytsche omzetters werden weer verwijderd. Vervolgens werd met 5 ieder voertuig 643,6 km (400 mijl) in totaal gereden, waarbij de kilometers gemaakt werden volgens een rijschema van autoweg/stadsverkeer volgens Automative Environmental Systems, Ine. Dit aantal kilometers werd gereden met XRG toevoegsel in de commerciële brandstof zonder lood. Het toevoegsel, dat gébruikt werd voor het kilometers maken en voor de na het rijschema 10 uitgevoerde proeven was niet hetzelfde toevoegsel als bij de vorige proef-reeksen gebruikt werd. Alle toevoegsel waren niet gemerkt. Na het rij-programma van het genoemde aantal kilometers werden met de voertuigen weer FTP/HFET-reeksen uitgevoerd met duplicaat proeven.The catalytic converters were removed again. Then, each vehicle drove 643.6 km (400 miles) in total, mileage was measured according to a road / city traffic schedule according to Automative Environmental Systems, Ine. This mileage was driven with XRG additive in the commercial unleaded fuel. The additive used for mileage and for the tests carried out after the driving schedule was not the same additive as used in the previous test runs. All additives were not labeled. After the driving program of the aforementioned mileage, FTP / HFET series were again performed with the vehicles with duplicate tests.
Tussen de basislijn FTP/HFET proef en het rijschema met het tweede toe-15 voegsel liepen de voertuigen gemiddeld 2690 km (1672 mijl). De Chevrolet Monte Carlo (no. 0051) legde 2560 km (1591 mijl) af; de Ford LTD (no. 0052) legde 2780 km (1740 mijl) af; en de Buick Regal (no. 0053) legde 2713 km (1686 mijl) af. Deze aantallen kilometers werden gereden met en zonder katalytische omzetters, met ongelode brandstof uit de handel en met onge-20 lode brandstof uit de handel met een toevoegsel.The vehicles ran an average of 2690 km (1672 miles) between the baseline FTP / HFET test and the driving schedule with the second add-on. The Chevrolet Monte Carlo (no. 0051) covered 2560 km (1591 miles); the Ford LTD (no. 0052) covered 2780 km (1740 miles); and the Buick Regal (no. 0053) covered 2,713 km (1,686 miles). These mileage were driven with and without catalytic converters, with unleaded commercial fuel and with unleaded commercial fuel with an additive.
Tabel 1 heeft betrekking op cuprisulfaat met de samenstelling van de uitvinding, aangeduid als toevoegsel I.Table 1 relates to cupric sulfate having the composition of the invention, designated as additive I.
Tabel 2 heeft betrekking op ferrosulfaat onder toepassing van de samen-' stelling als vermeld in kolom 1 van het Amerikaanse octrooischrift 25 4.145.190 van Webb.Table 2 refers to ferrous sulfate using the composition disclosed in column 1 of Webb's U.S. Patent No. 4,145,190.
80204728020472
Ol'O/'-'LCOl'O / '-' LC
- 6 -TABEL 1 Cuprisulfaat- 6 TABLE 1 Cupric Sulphate
Samenvatting van brandstofbesparingFuel Saving Summary
Voertuig no. Proef Zonder toe- Met toe- % Wijziging ; _ _ voegsel voegsel _ CX051 FTP 14,439 14,971 +3,7 HFET 18,933 19,760 +4,4 CX0052 FTP 13,724 14,669 +6,9 HFET 20,477 22,055 +7,7 10 CX0053 FTP 14,969 16,159 +7,9 HFET 19,281 21,185 · +9,9 , Gemiddeld over FTP 14,359 15,240 +6,1 totaal HEET i9/542 20,957 +7,2 TABEL 2 ,Ferrosulfaat 15Vehicle no. Test Without allow- With allowance% Change; _ _ grout grout _ CX051 FTP 14,439 14,971 +3,7 HFET 18,933 19,760 +4,4 CX0052 FTP 13,724 14,669 +6,9 HFET 20,477 22,055 +7,7 10 CX0053 FTP 14,969 16,159 +7,9 HFET 19,281 21,185 +9 , 9, Average over FTP 14,359 15,240 + 6.1 total HOT i9 / 542 20,957 + 7.2 TABLE 2, Ferrous sulfate 15
Samenvatting van brandstofbesparingFuel Saving Summary
Voertuig no. Proef Zonder toe- Met toe- % Wijziging __ _ voegsel' voegsel _ CX0051 FTP 14,182 14,345 +1,1 HFET 19,125 19,380 +1,3 20 CX0052 FTP 14,088 14,999 +6,5 HFET 22,864 22,798 -0,3 CX0053 FTP 15,793 15,582 -1,3 HFET 20,554 19,852 -3,4Vehicle no. Trial Without add- With% Change __ _ grout 'grout _ CX0051 FTP 14,182 14,345 +1.1 HFET 19,125 19,380 +1,3 20 CX0052 FTP 14,088 14,999 +6,5 HFET 22,864 22,798 -0,3 CX0053 FTP 15,793 15,582 -1.3 HFET 20,554 19,852 -3.4
Gemiddeld over FTP 14,648 14,958 +2,1 25 totaal HFET 20,736 20,571 -0,8 8020472 iAverage over FTP 14,648 14,958 +2.1 25 total HFET 20,736 20,571 -0.8 8020472 i
Claims (10)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US8001509 | 1980-11-12 | ||
PCT/US1980/001509 WO1982001717A1 (en) | 1980-11-12 | 1980-11-12 | Copper catalyst for fuels |
Publications (1)
Publication Number | Publication Date |
---|---|
NL8020472A true NL8020472A (en) | 1982-10-01 |
Family
ID=22154644
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NL8020472A NL8020472A (en) | 1980-11-12 | 1980-11-12 | COPPER FUEL CATALYST. |
NL8020447A NL8020447A (en) | 1980-11-12 | 1980-11-17 | ADDITIVES OR COMPOSITIONS FOR PETROL AND DIESEL FUELS TO INCREASE THE FLASH POINT. |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NL8020447A NL8020447A (en) | 1980-11-12 | 1980-11-17 | ADDITIVES OR COMPOSITIONS FOR PETROL AND DIESEL FUELS TO INCREASE THE FLASH POINT. |
Country Status (8)
Country | Link |
---|---|
EP (2) | EP0064494A4 (en) |
JP (2) | JPS57501854A (en) |
AU (1) | AU6645781A (en) |
BR (1) | BR8009120A (en) |
DE (1) | DE3050641A1 (en) |
GB (2) | GB2099850A (en) |
NL (2) | NL8020472A (en) |
WO (2) | WO1982001717A1 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
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GB2280200B (en) * | 1993-06-28 | 1997-08-06 | Exonflame Limited | Fuel oil additives |
GB2330149A (en) * | 1997-10-10 | 1999-04-14 | Sayed Ahmed | Fuel additive for the reduction of post-combustion pollutants |
CN1896197B (en) * | 2006-06-26 | 2011-04-06 | 于涛 | Methanol modified mixer |
USD862834S1 (en) | 2016-06-27 | 2019-10-15 | Mondelez Europe Gmbh | Cracker |
USD879408S1 (en) | 2016-06-06 | 2020-03-31 | Mondelez Europe Gmbh | Cracker |
USD887666S1 (en) | 2017-05-19 | 2020-06-23 | Generale Biscuit | Food bar |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE535369A (en) * | ||||
US1419910A (en) * | 1917-10-12 | 1922-06-20 | Us Ind Alcohol Co | Liquid fuel |
US1271114A (en) * | 1917-10-12 | 1918-07-02 | Us Ind Alcohol Co | Liquid fuel. |
US1669181A (en) * | 1924-05-10 | 1928-05-08 | Chester A Walter | Fuel for internal-combustion engines and motors |
US1820983A (en) * | 1926-02-15 | 1931-09-01 | Standard Oil Dev Co | Heavy oil fuel |
GB743472A (en) * | 1951-03-01 | 1956-01-18 | Power Jets Res & Dev Ltd | Improvements in or relating to fuel oils and the combustion of fuel oils |
US2962439A (en) * | 1956-12-07 | 1960-11-29 | Sun Oil Co | Fuel and lubricant additives for reducing combustion chamber deposits |
US4145190A (en) * | 1977-06-24 | 1979-03-20 | Natural Resources Guardianship International, Inc. | Catalytic fuel additive for jet, gasoline, diesel, and bunker fuels |
US4099930A (en) * | 1977-04-01 | 1978-07-11 | Natural Resources Guardianship International, Inc. | Catalytic fuel additive for gasoline and diesel engines |
US4188205A (en) * | 1978-03-06 | 1980-02-12 | Alchem, Inc. | Fuel injection in blast furnaces |
US4242100A (en) * | 1979-10-15 | 1980-12-30 | Tri-Pak, Inc. | Motor fuel composition |
-
1980
- 1980-11-12 JP JP50025781A patent/JPS57501854A/ja active Pending
- 1980-11-12 WO PCT/US1980/001509 patent/WO1982001717A1/en not_active Application Discontinuation
- 1980-11-12 GB GB8219351A patent/GB2099850A/en not_active Withdrawn
- 1980-11-12 NL NL8020472A patent/NL8020472A/en unknown
- 1980-11-12 BR BR8009120A patent/BR8009120A/en unknown
- 1980-11-12 EP EP19810900105 patent/EP0064494A4/en not_active Withdrawn
- 1980-11-12 DE DE19803050641 patent/DE3050641A1/en not_active Withdrawn
- 1980-11-12 AU AU66457/81A patent/AU6645781A/en not_active Abandoned
- 1980-11-17 WO PCT/US1980/001530 patent/WO1982001718A1/en not_active Application Discontinuation
- 1980-11-17 EP EP19800902355 patent/EP0064974A4/en not_active Withdrawn
- 1980-11-17 GB GB8219352A patent/GB2099774A/en not_active Withdrawn
- 1980-11-17 NL NL8020447A patent/NL8020447A/en not_active Application Discontinuation
- 1980-11-17 JP JP50010580A patent/JPS57501853A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
EP0064494A4 (en) | 1983-03-15 |
JPS57501854A (en) | 1982-10-14 |
WO1982001717A1 (en) | 1982-05-27 |
NL8020447A (en) | 1982-10-01 |
JPS57501853A (en) | 1982-10-14 |
EP0064974A4 (en) | 1983-03-15 |
GB2099774A (en) | 1982-12-15 |
EP0064974A1 (en) | 1982-11-24 |
AU6645781A (en) | 1982-06-07 |
WO1982001718A1 (en) | 1982-05-27 |
EP0064494A1 (en) | 1982-11-17 |
DE3050641A1 (en) | 1982-12-30 |
GB2099850A (en) | 1982-12-15 |
BR8009120A (en) | 1982-10-13 |
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