JPH0347894A - Fuel modifier - Google Patents

Fuel modifier

Info

Publication number
JPH0347894A
JPH0347894A JP1113246A JP11324689A JPH0347894A JP H0347894 A JPH0347894 A JP H0347894A JP 1113246 A JP1113246 A JP 1113246A JP 11324689 A JP11324689 A JP 11324689A JP H0347894 A JPH0347894 A JP H0347894A
Authority
JP
Japan
Prior art keywords
oil
modifier
fuel
solution
gasoline
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.)
Granted
Application number
JP1113246A
Other languages
Japanese (ja)
Other versions
JPH0515755B2 (en
Inventor
Jun Nasu
那須 醇
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.)
Individual
Original Assignee
Individual
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.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to KR1019890019591A priority Critical patent/KR940009045B1/en
Priority to US07/498,222 priority patent/US5087267A/en
Priority to CA002013367A priority patent/CA2013367A1/en
Priority to DE90106426T priority patent/DE69002790T2/en
Priority to AT90106426T priority patent/ATE93263T1/en
Priority to EP19900106426 priority patent/EP0394715B1/en
Priority to US07/583,143 priority patent/US5011502A/en
Priority to AU63028/90A priority patent/AU624053B2/en
Priority to CN90108990A priority patent/CN1027901C/en
Priority to SU904831321A priority patent/RU2024590C1/en
Priority to ES90118980T priority patent/ES2055267T3/en
Priority to EP90118980A priority patent/EP0478828B1/en
Priority to DK90118980.3T priority patent/DK0478828T3/en
Priority to DE69008176T priority patent/DE69008176T2/en
Publication of JPH0347894A publication Critical patent/JPH0347894A/en
Publication of JPH0515755B2 publication Critical patent/JPH0515755B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS 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
    • C10L10/00Use of additives to fuels or fires for particular purposes
    • C10L10/02Use of additives to fuels or fires for particular purposes for reducing smoke development

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Liquid Carbonaceous Fuels (AREA)

Abstract

PURPOSE:To obtain a modifier capable of enhancing the thermal efficiency of petroleum fuels such as gasoline and light oil and of suppressing toxic exhaust gas production by removing water from a seawater solution of a reaction product from an oil and strongly alkaline agent and dissolving the resultant solid in a solvent compatible with a fuel to be used. CONSTITUTION:A reaction product from (A) an oil such as a fractionated oil from waste tires and (B) an strongly alkaline agent at the mixing ratio ca.(0.5:1)-(1:0.5) is dissolved in seawater to prepare a ca.1-10% solution. Water is removed from the solution to obtain a solid, which is then dissolved in a solvent (pref. a mixed solvent consisting of kerosene and an alcohol such as butanol) compatible with a fuel to be used, thus obtaining the objective modifier. The amount of this modifier to be added is such as to be e.g. 0.1-0.3wt.%, 0.3-0.5wt.% and ca.1wt.% for gasoline, light oil and heavy oil, respectively.

Description

【発明の詳細な説明】 [産業上の利用分野コ この発明は、ガソリン、軽油等の石油系燃料の熱効率等
を改良し且つ燃焼時の有害な排ガスの発生を低減するた
めの燃料の改質剤に関する。
[Detailed Description of the Invention] [Industrial Field of Application] This invention relates to the reforming of petroleum fuels such as gasoline and diesel oil to improve their thermal efficiency and reduce the generation of harmful exhaust gases during combustion. Regarding drugs.

[従来の技術] 一般に自動車エンジン等の火花点火エンジンにおいては
エンジンの圧縮比が高い程熱効率は高く、出力が増大し
、燃費が向上するが、通常のガソリンの場合、圧縮比を
高くすると異常撚ガCやノッキングを生じかえって熱効
率が低下する。
[Prior Art] In general, in spark ignition engines such as automobile engines, the higher the compression ratio of the engine, the higher the thermal efficiency, the greater the output, and the better the fuel efficiency.However, in the case of ordinary gasoline, when the compression ratio is high, abnormal twisting occurs. This will cause gas and knocking, resulting in a decrease in thermal efficiency.

このため、アンチノック性の高いオクタン価の高いガソ
リンを用いることによって圧縮比を高め熱効率を向上さ
せているが、一般にオクタン価の高いガソリンは各種の
ガソリン調合材を適当な割合で配合して作られるため高
価である。
For this reason, gasoline with a high octane number and high anti-knock properties is used to increase the compression ratio and improve thermal efficiency. However, gasoline with a high octane number is generally made by blending various gasoline blending materials in appropriate proportions. It's expensive.

また、ガソリンの酸化による劣化はオクタン価の低下と
高分子ガム質による燃料消費の著しい悪化をもたらす。
Furthermore, deterioration of gasoline due to oxidation causes a decrease in octane number and a significant deterioration in fuel consumption due to the polymer gum quality.

このため、市販のガソリンには酸化防止剤を添加する必
要がある。
For this reason, it is necessary to add antioxidants to commercially available gasoline.

一方、ディーゼルエンジン(圧縮点火エンジン)の燃料
として用いられる軽油においては安定性の他、流動性、
着火性が問題となり、このため着火性の良好なセタン価
の高い軽油が必要となるが、セタン価の高い軽油もまた
、一般の軽油に比べ高価である。
On the other hand, light oil used as fuel for diesel engines (compression ignition engines) has not only stability but also fluidity and
Ignitability becomes a problem, and therefore a light oil with a high cetane number and good ignitability is required, but light oil with a high cetane number is also more expensive than ordinary light oil.

また、軽油が酸化劣化するとガソリンの場合と同様に高
分子量のガム質が生成し、これが大量に生成すると燃料
噴射ノズルを閉塞し、燃料の供給を阻害する。このよう
な軽油の劣化による問題を防止するためには水素化精製
等が必要となる。
Furthermore, when light oil deteriorates due to oxidation, a high-molecular-weight gum is produced in the same manner as in the case of gasoline, and when this is produced in large quantities, it clogs the fuel injection nozzle and obstructs the supply of fuel. In order to prevent such problems due to deterioration of light oil, hydrorefining and the like are required.

このような従来の問題点を解決するものとして本発明の
発明者は海水中の元素の有効利用及び燃焼時におけるア
ルカリ剤の作用に着目し、海水に特殊なアルカリ剤を溶
解させて成る燃焼助剤(特開昭63−225695号)
を開発し燃焼性の向上に関し著しい効果を収めた。
In order to solve these conventional problems, the inventor of the present invention focused on the effective use of elements in seawater and the action of alkaline agents during combustion, and developed a combustion aid made by dissolving a special alkaline agent in seawater. agent (JP-A No. 63-225695)
Developed and achieved remarkable results in improving flammability.

そして、この燃焼助剤(水溶液)は特に噴霧状でエンジ
ンに添加することによって特に優れた効果をもたらすこ
とをつきとめ、この燃焼助剤をエンジンに添加するため
のシステムを開発した(特開昭63−147938号、
特願昭62−319827号)。
He discovered that this combustion aid (aqueous solution) had particularly excellent effects when added to the engine in the form of a spray, and developed a system for adding this combustion aid to the engine (Japanese Patent Laid-Open No. 63 -147938,
(Patent Application No. 319827/1982).

しかし、この燃焼助剤はエンジン等の改造を必要とする
ので、直ちにすべての自動車に適用することはできなか
った。特に、上記システムはピストンの負圧で混合ガス
を送るシステム用に開発されているため、ターボエンジ
ンに適用する場合、圧力をかけて燃焼助剤を供給しなけ
ればならず高度なシステムを必要とし、技術的に困難な
点が多石油の各留分、プラスチック、古タイヤ等の分留
オイル、廃油等の油に、貝から、石灰石等の高温焼成物
のような酸化カルシウムを主成分とする強アルカリ剤の
粉末を加え若干の水の存在下で撹拌、混合し反応させて
得られる粉末である。油と強アルカリ剤の混合比及び加
える水の量は、油の種類によって異なるが、通常油対強
アルカリ剤の混合比が0.5: 1から1.:0.5程
度、水はO〜10%程度添加する。
However, since this combustion aid requires modification of the engine, etc., it could not be immediately applied to all automobiles. In particular, the above system was developed for a system that delivers the mixed gas under the negative pressure of the piston, so when applied to a turbo engine, the combustion aid must be supplied under pressure, requiring a sophisticated system. , There are many technically difficult points, such as various fractions of petroleum, fractionated oils such as plastics and old tires, oils such as waste oil, and oils such as shellfish and high-temperature calcined products such as limestone that have calcium oxide as the main component. It is a powder obtained by adding powder of a strong alkaline agent and stirring and mixing it in the presence of some water to cause a reaction. The mixing ratio of oil and strong alkaline agent and the amount of water to be added vary depending on the type of oil, but usually the mixing ratio of oil to strong alkaline agent is 0.5:1 to 1. : Approximately 0.5%, and water is added in an amount of approximately 0 to 10%.

この油とアルカリ剤との反応物は、油とアルカリ剤とが
結合したマクロ的には均一な粉状体であり、海水に対し
1〜10%加え撹拌後放置することにより溶解し均一な
溶液(a)となる。この際海水は予め低PHないし高p
Hに調整しておくことが望ましい。また不溶物があれば
除去する。この溶液(a)は前述のようにそれ自体、燃
焼状態を改善する燃焼助剤として機能するものであるが
、水溶液であるため、特殊な方法でなければ燃焼系に適
用することはできない。
This reaction product of oil and alkaline agent is a macroscopically uniform powder in which oil and alkaline agent are combined, and when added to seawater at 1 to 10% and stirred and left to stand, it dissolves and forms a uniform solution. (a) becomes. At this time, the seawater has a low pH or a high pH.
It is desirable to adjust it to H. Also, remove any insoluble matter. As mentioned above, this solution (a) itself functions as a combustion aid that improves combustion conditions, but since it is an aqueous solution, it cannot be applied to a combustion system without a special method.

本発明の燃料の改質剤は、この溶液(a)からかった。The modifier of the fuel of the present invention was mixed with this solution (a).

[発明の目的コ この発明はこのような従来の目的を解決し、ガソリン、
軽油、灯油等のあらゆる液体燃料に直接添加することが
でき、′これら液体燃料の燃焼状態を改善することので
きる燃料の改質剤を提供することを目的とする。更に、
本発明は、あらゆる自動車等の内燃機関に適用でき、内
燃機関の燃費効率を高め有害な排ガスの低減を図ること
のできる燃料の改質剤を提供することを目的とする。
[Purpose of the Invention] This invention solves the conventional object,
The object of the present invention is to provide a fuel modifier that can be directly added to any liquid fuel such as light oil or kerosene, and can improve the combustion conditions of these liquid fuels. Furthermore,
An object of the present invention is to provide a fuel modifier that can be applied to internal combustion engines of all kinds of automobiles and can improve the fuel efficiency of the internal combustion engine and reduce harmful exhaust gases.

[課題を解決するための手段] このような目的を達成する本発明の燃料の改質剤は、油
と強アルカリ剤との反応物を海水に溶解した溶液(a)
から水分を除去した後の固体(b)を適用される燃料と
相溶性の溶剤に溶解させたものからなる。
[Means for Solving the Problems] The fuel modifier of the present invention that achieves the above object is a solution (a) in which a reaction product of oil and a strong alkaline agent is dissolved in seawater.
The solid (b) after removal of moisture from the solid (b) is dissolved in a solvent compatible with the applied fuel.

ここで油と強アルカリ剤との反応物を海水に溶解した溶
液(a)とは特開昭63−225695号公報に記載さ
れる燃焼助剤そのものである。
The solution (a) in which a reaction product of oil and a strong alkaline agent is dissolved in seawater is exactly the combustion aid described in JP-A-63-225695.

すなわち、油と強アルカリ剤との反応物とは、− 水分を除去し、更に所定溶剤に溶解せしめたものである
That is, the reaction product of oil and a strong alkaline agent is one obtained by removing moisture and further dissolving it in a specified solvent.

溶液(a)から水分の除去するには、通常加熱蒸発によ
って行う。減圧下で行ってもよい。これにより固体(b
)を得る。この固体(b)の元素分析の結果を表1に示
す。
Water is usually removed from solution (a) by heating and evaporation. It may also be carried out under reduced pressure. This results in a solid (b
). Table 1 shows the results of elemental analysis of this solid (b).

表1 表1からも明らかなように固体(b)は海水中の元素に
比較し塩素がかなり減少しており強い塩基性の物質であ
る。
Table 1 As is clear from Table 1, the solid (b) contains considerably less chlorine than the elements in seawater and is a strongly basic substance.

溶剤としては固体(b)を溶解させるものであって、且
つ適用される燃料に対し相溶性がある溶剤を用いる。こ
のような溶剤として、好適にはアルコールと適当な有機
溶剤との混合溶剤が用いられる。有機溶剤としては灯油
が実用的である。灯油とアルコールとの混合比及び用い
るアルコールの種類は適用される燃料に応じて適宜選択
されるが、ガソリン、軽油の場合、アルコールとしては
メタノール、ブタノールあるいはこれらの混合物等が用
いられ、ブタノールを少なくとも溶剤全体の10%以上
含有することが好ましい。
As the solvent, a solvent that dissolves the solid (b) and is compatible with the applied fuel is used. As such a solvent, a mixed solvent of alcohol and a suitable organic solvent is preferably used. Kerosene is a practical organic solvent. The mixing ratio of kerosene and alcohol and the type of alcohol to be used are appropriately selected depending on the fuel to be used, but in the case of gasoline and diesel oil, methanol, butanol, or a mixture thereof is used as the alcohol. It is preferable that the content is 10% or more of the total solvent.

このように調整されたアルコールを含む混合溶剤に前述
の固体(b)を溶解させることにより本発明の燃料の改
質剤を得ることができる。混合溶剤に対する固体(b)
の濃度は約1%程度である。
The fuel modifier of the present invention can be obtained by dissolving the aforementioned solid (b) in the alcohol-containing mixed solvent prepared in this way. Solid (b) for mixed solvents
The concentration of is about 1%.

好適には、上記混合溶剤中に固体(b)を数%程度溶解
せしめた改質剤の原液を調整しておき、この原液をさら
に適用される燃料に適合するように強アルカリ剤を得る
Preferably, a stock solution of the modifier is prepared by dissolving several percent of the solid (b) in the mixed solvent, and this stock solution is further used to obtain a strong alkaline agent suitable for the fuel to be applied.

海水1000ccを酸で低pHにした後、上記強アルカ
リ剤20gを加え、約1時間撹拌した後沈殿物を除去し
、高PHに調整した海水を得た。
After 1000 cc of seawater was made to have a low pH with an acid, 20 g of the above-mentioned strong alkaline agent was added, and after stirring for about 1 hour, the precipitate was removed to obtain seawater adjusted to a high pH.

一方、古タイヤの分留オイル500ccに上記強アルカ
リ剤500gを加え、更に強アルカリ溶液100ccを
加え撹拌した後、約2気圧で30分放置し、粉末状の反
応物を得た。
On the other hand, 500 g of the above strong alkaline agent was added to 500 cc of fractionated old tire oil, 100 cc of a strong alkaline solution was added, and the mixture was stirred and left at about 2 atmospheres for 30 minutes to obtain a powdery reaction product.

pHを一旦2以下に調整した後更に約13に調整した海
水1000ccに上記反応物30gを加え反応器内で1
.5気圧、室温で約1時間撹拌した後約1昼夜放置し、
不溶物を除去した後均−な溶液(a)を得た。
After the pH was once adjusted to 2 or less, 30 g of the above reactant was added to 1000 cc of seawater whose pH was further adjusted to about 13, and the pH was adjusted to 1 in the reactor.
.. After stirring at 5 atm and room temperature for about 1 hour, leave it for about 1 day and night.
After removing insoluble matter, a homogeneous solution (a) was obtained.

次いで、この溶液(a)it加熱することによって水分
を除去し、固体(b)60kgを得た。
Next, water was removed from this solution (a) by heating it to obtain 60 kg of solid (b).

一方、下記の処方による灯油とアルコールとの混合溶剤
を調整し、これら混合溶剤に対しそれぞれ上記固体(b
)1kgを加え、撹拌混合することにより、改質剤の原
液を得た。
On the other hand, a mixed solvent of kerosene and alcohol was prepared according to the following formulation, and the above solid (b) was added to each of these mixed solvents.
) and stirred and mixed to obtain a stock solution of the modifier.

処方A 所定の混合溶剤で希釈することにより濃度及び溶剤組成
を調整する。改質剤の原液の元素分析の結果も併せて表
1に示す。
Formulation A Adjust the concentration and solvent composition by diluting with a specified mixed solvent. Table 1 also shows the results of elemental analysis of the stock solution of the modifier.

このように得られた本発明の燃料の改質剤はガソリン、
重油、軽油等の燃料に直接添加することによって使用さ
れる。
The thus obtained fuel modifier of the present invention is gasoline,
It is used by directly adding it to fuels such as heavy oil and light oil.

添加量は適用される燃料によって異なるが1例えばガソ
リンの場合0.1〜0.3%、軽油の場合0.3〜0.
5%、重油の場合1%程度添加することができる。
The amount added varies depending on the fuel to which it is applied; for example, in the case of gasoline, it is 0.1 to 0.3%, and in the case of diesel oil, it is 0.3 to 0.
It can be added in an amount of about 5%, or about 1% in the case of heavy oil.

本発明の改質剤の添加によって、いずれの燃料において
も燃料状態が顕著に改善され、燃焼効率が向上すると共
にHC,C○等の有害な排ガスの発生が減少する。
By adding the modifier of the present invention, the fuel condition of any fuel is significantly improved, the combustion efficiency is improved, and the generation of harmful exhaust gases such as HC and CO is reduced.

[実施例] 以下、実施例により説明する。[Example] Examples will be explained below.

帆立貝等の貝殻を水洗いした後、砕く。この砕いたもの
を炉に入れて1000℃〜1200℃で約30分間焼い
た後に、約1350℃に上げて5分〜10分間焼いて約
200メツシユの粉末状の一 メチルアルコール    6Q ブチルアルコール   10fl 灯油         14Q・ 処方B メチルアルコール    8Q ブチルアルコール   12Q 灯油         2(1 塗料用シンナー     4Q 処方C ブチルアルコール   0.50 塗料用シンナー     412 処方D メチルアルコール    5Q ブチルアルコール   12.5Q 処方A、処方りの原液10Qを灯油20Q及びブタノー
ル1.5Qからなる混合溶剤で希釈し、改質剤A、改質
剤りを得た。処方Cの原液2.5Qを灯油15jlk及
びブタノール6.5Qからなる混合溶剤で希釈し、改質
剤Cを得た。
After washing scallops and other shells with water, crush them. This crushed material is placed in a furnace and baked at 1000°C to 1200°C for about 30 minutes, then raised to about 1350°C and baked for 5 to 10 minutes to produce about 200 mesh of powdered monomethyl alcohol, 6Q butyl alcohol, 10 fl kerosene. 14Q. Prescription B Methyl alcohol 8Q Butyl alcohol 12Q Kerosene 2 (1 Paint thinner 4Q Prescription C Butyl alcohol 0.50 Paint thinner 412 Prescription D Methyl alcohol 5Q Butyl alcohol 12.5Q Prescription A, 10Q kerosene undiluted solution and 1.5Q of butanol to obtain modifier A and modifier.2.5Q of the stock solution of prescription C was diluted with a mixed solvent of kerosene 15jlk and butanol 6.5Q to obtain modifier A quality agent C was obtained.

実施例1.2 総排気量2000ccのガソリンエンジン車に上記の改
質剤A、改質剤りを各々ガソリン60Qに対し120c
c添加し、走行テストを行った。
Example 1.2 A gasoline engine vehicle with a total displacement of 2000 cc was treated with the above-mentioned modifier A and modifier R at a rate of 120 c per 60 Q of gasoline.
c was added and a running test was conducted.

15千km走行後の排気中のHC及びCOの分析結果及
び燃費効率を表2に示す。
Table 2 shows the analysis results of HC and CO in the exhaust after traveling 15,000 km and the fuel efficiency.

同機種のガソリン車で本発明の改質剤を使わない場合(
比較例1)の走行テストの結果も同様に表2に示す。
When the same type of gasoline car does not use the modifier of the present invention (
The results of the running test of Comparative Example 1) are also shown in Table 2.

表2 実施例3 ジーゼルエンジン車に上記の改質剤Aを軽油60flに
対し180cc添加し、走行テストを行った。15千k
m走行後の排気中の燃費効率及び黒煙測定の結果を表3
に示す。
Table 2 Example 3 180 cc of the above modifier A was added to 60 fl of diesel oil in a diesel engine vehicle, and a driving test was conducted. 15,000k
Table 3 shows the results of fuel efficiency and black smoke measurement in the exhaust after driving for m.
Shown below.

同機種のジーゼルエンジン車で本発明の改質剤を使わな
い場合(比較例2)の結果も同様に表3に示す。
Table 3 also shows the results of a diesel engine vehicle of the same model in which the modifier of the present invention was not used (Comparative Example 2).

表3 実施例4.5 上記の改質剤C1改質剤の原液Bをそれぞれ灯油ストー
ブ、重油ボイラーに燃料の約1%添加した。いずれの場
合も本発明の改質剤を使用しない場合に比べ燃焼状態が
良好で臭いや黒煙の発生がなく、また燃料の消費が少な
かった。
Table 3 Example 4.5 The above Modifier C1 Modifier stock solution B was added to a kerosene stove and a heavy oil boiler in an amount of about 1% of the fuel, respectively. In all cases, combustion conditions were better, no odor or black smoke was generated, and fuel consumption was lower than when the modifier of the present invention was not used.

[発明の効果] 以上の実施例からも明らかに本発明の改質剤によれば、
ガソリン車、ジーゼル車のいずれにおいても燃費を飛耀
的に向上させることができ、しかも排ガス中のHC,C
o等を低減することができる。
[Effect of the invention] It is clear from the above examples that according to the modifier of the present invention,
Fuel efficiency can be dramatically improved for both gasoline and diesel vehicles, and HC and C in exhaust gas can be dramatically improved.
o etc. can be reduced.

又、本発明の改質剤は、燃料中に直接添加できるので、
自動車等の内燃機関のみならず、ボイラ、ストーブ、そ
の他あらゆる燃焼機関に適用することかできる。
Furthermore, since the modifier of the present invention can be added directly to fuel,
It can be applied not only to internal combustion engines such as automobiles, but also to boilers, stoves, and all other combustion engines.

−11 12−-11 12-

Claims (1)

【特許請求の範囲】 1、油と強アルカリ剤との反応物を海水に溶解した溶液
(a)から水分を除去した後の固体(b)を適用される
燃料と相溶性の溶剤に溶解させたものから成る燃料の改
質剤。 2、前記溶剤はアルコールを含有することを特徴とする
第1項記載の燃料の改質剤。
[Claims] 1. After water is removed from a solution (a) in which a reaction product of oil and a strong alkaline agent is dissolved in seawater, the solid (b) is dissolved in a solvent compatible with the applied fuel. A fuel modifier consisting of 2. The fuel modifier according to item 1, wherein the solvent contains alcohol.
JP1113246A 1989-04-04 1989-05-02 Fuel modifier Granted JPH0347894A (en)

Priority Applications (14)

Application Number Priority Date Filing Date Title
KR1019890019591A KR940009045B1 (en) 1989-04-04 1989-12-27 Fuel additives
US07/498,222 US5087267A (en) 1989-04-04 1990-03-23 Fuel additives
CA002013367A CA2013367A1 (en) 1989-04-04 1990-03-29 Fuel additives
DE90106426T DE69002790T2 (en) 1989-04-04 1990-04-04 Fuel additives.
AT90106426T ATE93263T1 (en) 1989-04-04 1990-04-04 FUEL ADDITIVES.
EP19900106426 EP0394715B1 (en) 1989-04-04 1990-04-04 Fuel additives
US07/583,143 US5011502A (en) 1989-04-04 1990-09-17 Fuel additives
AU63028/90A AU624053B2 (en) 1989-04-04 1990-09-19 Fuel additives
CN90108990A CN1027901C (en) 1989-04-04 1990-09-29 Fuel additives
SU904831321A RU2024590C1 (en) 1989-04-04 1990-10-02 Process for preparing fuel additive
ES90118980T ES2055267T3 (en) 1989-04-04 1990-10-04 ADDITIVES FOR FUEL.
EP90118980A EP0478828B1 (en) 1989-04-04 1990-10-04 Fuel additives
DK90118980.3T DK0478828T3 (en) 1989-04-04 1990-10-04 fuel additives
DE69008176T DE69008176T2 (en) 1989-04-04 1990-10-04 Fuel additives.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP8524989 1989-04-04
JP1-85249 1989-04-04

Publications (2)

Publication Number Publication Date
JPH0347894A true JPH0347894A (en) 1991-02-28
JPH0515755B2 JPH0515755B2 (en) 1993-03-02

Family

ID=13853296

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1113246A Granted JPH0347894A (en) 1989-04-04 1989-05-02 Fuel modifier

Country Status (1)

Country Link
JP (1) JPH0347894A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0556727A (en) * 1991-02-26 1993-03-09 Watanabe Kikai Kogyo Kk Treatment of laver net and treating boat
JP2521319Y2 (en) * 1994-10-06 1996-12-25 渡辺機開工業株式会社 Nori net cleaning boat

Also Published As

Publication number Publication date
JPH0515755B2 (en) 1993-03-02

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