JPH0229712B2 - - Google Patents
Info
- Publication number
- JPH0229712B2 JPH0229712B2 JP56000624A JP62481A JPH0229712B2 JP H0229712 B2 JPH0229712 B2 JP H0229712B2 JP 56000624 A JP56000624 A JP 56000624A JP 62481 A JP62481 A JP 62481A JP H0229712 B2 JPH0229712 B2 JP H0229712B2
- Authority
- JP
- Japan
- Prior art keywords
- carrier
- fuel
- additive
- tablet
- composite
- 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.)
- Expired - Lifetime
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
- 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
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Carbon And Carbon Compounds (AREA)
- Detergent Compositions (AREA)
Description
【発明の詳細な説明】
本発明は、内燃機関に用いる燃料添加剤の複合
体に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a complex of fuel additives for use in internal combustion engines.
オツトサイクルエンジン、ヂーゼルサイクルエ
ンジン用の各種の燃料添加剤類が知られている。 Various fuel additives for oil cycle engines and diesel cycle engines are known.
これらの添加剤は、たとえば下記のような各種
の機能を達成するものである。 These additives accomplish various functions, such as those described below.
ガソリンのオクタン価を高め、又は、ヂーゼル
エンジンのセタン価を高める。 Increase the octane number of gasoline or the cetane number of diesel engines.
腐蝕を防止し、洗剤効果を発揮する。 Prevents corrosion and exerts detergent effect.
酸化及びゴム状物、ラツカー状物の生成を防止
する。 Prevents oxidation and the formation of rubbery and lacquer-like substances.
ヂーゼルサイクルエンジンの場合には、煙の発
生を減少させる。 In the case of diesel cycle engines, it reduces smoke production.
これらの用途上、添加剤は、内燃機関に用いる
炭化水素類に可溶性でなければならない。そし
て、常温で通常液状である。添加剤は、燃料に少
量添加しなければならない。この種の添加剤は、
溶剤、鉱物油、合成油に配合して市販されてい
る。したがつて、小分けしたり、計量したりする
ようになつている。しかしながら、直接の使用者
は、しばしば種々の困難を感じる。たとえば、モ
ータリストやドライバーは、燃料の量に応じた容
量の液状を添加剤量を、車の燃料タンクに入れな
ければならなかつた。市販等の添加剤を燃料タン
クへ罐から入れたり、小さな計量器で入れたりす
ることによつて過少だつたり、過剰だつたりする
誤りが起る。 For these applications, the additive must be soluble in the hydrocarbons used in internal combustion engines. It is usually liquid at room temperature. Additives must be added to the fuel in small quantities. This type of additive is
It is commercially available mixed with solvent, mineral oil, and synthetic oil. As a result, people have begun to divide and measure food into smaller portions. However, direct users often experience various difficulties. For example, motorists and drivers have had to fill their car's fuel tank with a volume of liquid additive that corresponds to the amount of fuel. Errors such as adding too much or too little additives can occur by adding commercially available additives to the fuel tank from a can or using a small meter.
精製業者、貯蔵業者、貯蔵所は、濃厚な態様で
添加剤を用いており、この場合には、正確な計量
をおこなうことが容易である。しかしながら、価
格上の問題で、未添加燃料又は、最低限の添加剤
を配合した燃料を販売せざるを得ないこととなつ
ている。 Refiners, stockpilers, and depots use additives in concentrated form, where it is easier to do accurate metering. However, due to price issues, it is necessary to sell fuel without additives or fuel with a minimum amount of additives.
しかして、消費者又は使用者によつて容易にす
ぐに利用出来かつ、面倒な計量なしに、むだな
く、直接に使用しうる燃料用添加剤の市販の要望
が見られる。 There is thus a commercial need for fuel additives that are easily and readily available to the consumer or user and can be used directly, without tedious metering, and without waste.
本発明によれば、この種の要望は、固型、好ま
しくは、錠剤であつて、各錠剤が特定の燃料容積
たとえば10リツター当りの割合になつている錠剤
を用いることによつて達成されるものである。 According to the invention, this type of desire is achieved by using solid, preferably tablets, each tablet being proportioned to a specific fuel volume, for example 10 liters. It is something.
それ故、消費者又は、使用者たとえば、モータ
リスト又は運転者は、たとえば燃料を入れたとき
に、タンクに給油した燃料数+リツター当り何粒
かの錠剤をタンク中に入れれば済む。 Therefore, the consumer or user, for example a motorist or a driver, only has to place into the tank, for example, when filling it with fuel, the number of tablets per liter plus the number of fuels filled in the tank.
この種の目的を達成するために、本発明は、室
温又は常態で固定の担体であつて、炭化水素を主
として含有する液状炭化水素可溶性の担体に、該
燃料用添加剤を配合したことを特徴とする燃料用
添加剤と担体その複合体からなるものである。 In order to achieve this kind of object, the present invention is characterized in that the fuel additive is blended into a liquid hydrocarbon-soluble carrier that is fixed at room temperature or under normal conditions and mainly contains hydrocarbons. It consists of a composite of a fuel additive and a carrier.
該炭化水素類は、非環式、脂環式又は芳香族炭
化水素類であつて、それぞれ、非環式炭化水素は
少なくとも17炭素原子以上、脂環式炭化水素は少
なくとも12炭素原子以上、芳香族炭化水素は少な
くとも10炭素原子以上のものである。 The hydrocarbons are acyclic, alicyclic, or aromatic hydrocarbons, and acyclic hydrocarbons are at least 17 carbon atoms, alicyclic hydrocarbons are at least 12 carbon atoms, aromatic Group hydrocarbons are those having at least 10 carbon atoms.
本発明によれば、ナフタレンを担体として用い
ることが特に好ましい。 According to the invention, it is particularly preferred to use naphthalene as carrier.
本発明の固体複合体は、各種の方法で製造する
ことが出来る。特に好ましい方法は、下記の方法
である。 The solid composite of the present invention can be produced by various methods. A particularly preferred method is the method described below.
加熱法
該担体を溶融し、該添加剤をこの中に融解す
る。この流動性混合物を冷却することによつて、
所望の量の該添加剤を配合した錠剤を製造する。Heating method The carrier is melted and the additives are melted therein. By cooling this fluid mixture,
A tablet containing the desired amount of the additive is manufactured.
非加熱法
該担体を所望の粒度にまで粉砕し、粉砕した担
体を撹拌しながら、該添加剤を吸収させ、得られ
た混合物を加圧して、所望の量の添加剤を含む錠
剤とする。Non-heating method The carrier is ground to the desired particle size, the additive is absorbed while stirring the ground carrier, and the resulting mixture is pressurized to form tablets containing the desired amount of additive.
実施例によつて、本発明をさらに説明する。 The invention will be further illustrated by examples.
実施例 1
ガソリン用多機能添加剤の製法(ホツト法)
精製ナフタレン838Kgを2000リツトルのステン
レス鋼製の容器に入れ、加熱して溶融物の温度を
82℃とし、撹拌しながら、この温度を保つた。こ
の溶融物中に、多価添加剤(商品名Lubrizol
8101として市販の添加剤Lubrizol Corp社製)
159.5Kgを撹拌しながら添加混合した。混合物を
20℃に冷却し、公知方法で142500個の錠剤とし
た。各錠剤は5,88gの担体と1.12gのガソリン
添加剤とを含有しており、ガソリン10リツトルに
対して1錠の割合で用いた。Example 1 Method for producing a multifunctional additive for gasoline (hot method) 838 kg of purified naphthalene was placed in a 2000 liter stainless steel container and heated to bring the temperature of the molten material to a
The temperature was brought to 82° C. and maintained at this temperature with stirring. A polyvalent additive (trade name: Lubrizol) is added to this melt.
Additive commercially available as 8101 (manufactured by Lubrizol Corp.)
159.5Kg was added and mixed while stirring. mixture
It was cooled to 20°C and made into 142,500 tablets using a known method. Each tablet contained 5.88 g of carrier and 1.12 g of gasoline additive, and was used at a rate of 1 tablet per 10 liters of gasoline.
実施例 2
ガソリン用多機能添加剤の製法(コールド法)
精製ナフタレン1000Kgをボールミルで粉砕し
800メツシユ/cm2のふるいを通して、ふるい分け
して、986Kgの粉砕された粉末を得た。これをス
テンレス鋼容器に入れ、撹拌しながらガソリン添
加剤134Kgを加えた。添加剤は商品名A577として
アモコ社(Amoco InternationalS.A.スイス)か
ら市販されているものを用いた。20分後に、該添
加剤は完全に吸収された。公知の錠剤機を用い
て、160000個の錠剤を製造した。各錠剤は、6.16
gの担体と0.84gのガソリン添加剤とを含有して
おり、ガソリン15リツトルに対して1錠の割合で
用いた。Example 2 Production method of multifunctional additive for gasoline (cold method) 1000 kg of purified naphthalene was ground in a ball mill.
Screening through an 800 mesh/cm 2 sieve yielded 986 Kg of ground powder. This was placed in a stainless steel container and 134Kg of gasoline additive was added while stirring. The additive used was one commercially available from Amoco International S.A. (Switzerland) under the trade name A577. After 20 minutes the additive was completely absorbed. 160,000 tablets were manufactured using a known tablet machine. Each tablet is 6.16
The tablet contained 1 g of carrier and 0.84 g of gasoline additive, and was used at a rate of 1 tablet per 15 liters of gasoline.
実施例 3
自動車のヂーゼル油用の多目的添加剤の精法、
非加熱法。Example 3 Process for refining a multi-purpose additive for automobile diesel oil,
Non-heating method.
工業用純ナフタレン812Kgをボールミル中で粉
砕し、次いで、800メツシユ/cm2のふるいを通し
てふるい分けし、800Kgの粉砕ナフタレンを得た。
これをステンレス鋼の容器に入れ、撹拌しながら
200Kgの添加剤をこれに加えた。該添加剤は、市
販のエチル社(米国)のMPA−D.及びD112であ
つて、下記の組成を有するものである。 812 Kg of industrially pure naphthalene was ground in a ball mill and then sieved through a 800 mesh/cm 2 sieve to obtain 800 Kg of ground naphthalene.
Pour this into a stainless steel container and stir
200Kg of additives were added to this. The additives are commercially available MPA-D. and D112 from Ethyl Corporation (USA) and have the following composition.
MPA−Dを55〜35%とD112を45〜65%配合し
たものである。25分後に、該添加剤は完全に吸収
された。公知の錠剤製造機によつて、これから、
80000個の錠剤を製造した。各錠剤は、10gの担
体と2.5gの添加剤とを含有していた。これは、
ヂーゼル油5リツトル当り1錠剤の割合で用いる
に適した割合のものである。 It is a blend of 55-35% MPA-D and 45-65% D112. After 25 minutes the additive was completely absorbed. From now on, using a known tablet making machine,
80,000 tablets were manufactured. Each tablet contained 10 g carrier and 2.5 g excipients. this is,
The ratio is suitable for use at the rate of 1 tablet per 5 liters of diesel oil.
しかして、この得られた固体錠剤は、消費者又
は使用者が直接に用いるものである。 The resulting solid tablets are then used directly by the consumer or user.
(錠剤として得られる固体複合体の例)
実施例 A
非環式炭化水素を担体として用いる燃料用オク
タン価改善剤の製法(コールド法)
密閉式鋼製混合機に、n−ドトリアコンタン
(C32H66)156.8kgを入れ、メチルシクロペンタ
ジエニトリカルボニルマンガン塩43.2kgを加え
た。なお、このマンガン塩は、マンガン塩43.2kg
に対し、0.20kgの割合で既知の脂溶性染料で予め
赤色に着色しておいた。(Example of a solid composite obtained as a tablet) Example A Method for producing an octane number improver for fuel using an acyclic hydrocarbon as a carrier (cold method) In a closed steel mixer, n-dotriacontane (C 32 156.8 kg of H 66 ) was added, and 43.2 kg of methylcyclopentadienytricarbonylmanganese salt was added. In addition, this manganese salt is 43.2 kg of manganese salt.
On the other hand, 0.20 kg of the sample was previously colored red with a known fat-soluble dye.
液状層が完全に吸収されるまで攪拌を続け、約
30分後に、10g中に9.57gの担体と0.43gの有機
マンガン塩を含む錠剤100000個を既知の方法によ
り得た。 Continue stirring until the liquid layer is completely absorbed, approx.
After 30 minutes, 100,000 tablets containing 9.57 g of carrier and 0.43 g of organic manganese salt in 10 g were obtained by a known method.
この錠剤1個は、ガソリン20リツトルに対して
使われ、有効成分の平均処理濃度は30ppmであ
る。 One tablet is used for 20 liters of gasoline, and the average treatment concentration of active ingredient is 30 ppm.
実施例 B
脂環式炭化水素を坦体として用いる2サイクル
エンジンのならし運転(breaking−in)用の耐
摩耗剤の製法(コールド法)
鋼製の混合機に、シクロテトラデカン
(C14H28)54kgと4,4−メチレンビス(2,6
−ジ−ターシヤリーブチルフエノール)96kgを
入れた。室温で、ゆつくりと約15分間攪拌した
後、1錠3gあたり担体1.08gと2リツトルの燃
料に対して使われる耐摩耗フエノール性添加剤
1.92gを含有する錠剤50000個を既知の方法で製
造した。Example B Method for producing an anti-wear agent for breaking-in of a two-stroke engine using an alicyclic hydrocarbon as a carrier (cold method) In a steel mixer, cyclotetradecane (C 14 H 28 )54kg and 4,4-methylenebis(2,6
- 96 kg of di-tertiary butylphenol) was added. Anti-wear phenolic additive used for 1.08 g of carrier and 2 liters of fuel per 3 g tablet after stirring gently for approximately 15 minutes at room temperature.
50,000 tablets containing 1.92 g were manufactured by known methods.
実施例 C
芳香族炭化水素を担体として用いるジーゼル燃
料用抗発煙添加剤の製法(ホツト法)
2000リツトルのステンレス製容器に溶かしたフ
エニルベンゾール(C12H10)1042kgを入れた。
溶かした原料を攪拌しながら75〜80℃に保ちつ
つ、アミン塩と脂肪族アミンの有機酸塩から成る
と思われるHITEC 4201として知られるエチルコ
ーポレーシヨン(EthylCoporation(U.S.A))製
の添加剤168kgをゆつくりと加えた。溶けた原料
中にエチル社製の添加剤が完全に溶解した後、反
応温度を20℃にし、次にジーゼル燃料10リツトル
を処理するのに用いる1錠中にエチル社製の添加
剤1.67kg及び担体10.33gを含む錠剤100800個を、
既知の方法で製造した。Example C Method for producing an anti-smoke additive for diesel fuel using an aromatic hydrocarbon as a carrier (hot method) 1042 kg of dissolved phenylbenzole (C 12 H 10 ) was placed in a 2000 liter stainless steel container.
While stirring and maintaining the melted raw material at 75-80°C, 168 kg of an additive manufactured by Ethyl Corporation (USA) known as HITEC 4201, which is believed to be composed of amine salts and organic acid salts of aliphatic amines, was added. I added it slowly. After the Ethyl additive is completely dissolved in the melted raw material, the reaction temperature is raised to 20°C, and then 1.67 kg of the Ethyl additive is mixed into one tablet used to treat 10 liters of diesel fuel. 100,800 tablets containing 10.33g of carrier,
Manufactured by known methods.
(錠剤以外の形で得られる固体複合体の例)
実施例 D
固体顆粒状のセタン価改善剤の製法(コールド
法)
適当な鋼製の混合機にデユレタン(1,2,
4,5−テトラメチルベンゼン)(C10H16)
1200kgと脂溶性の青色染料0.1kgで予め青色に染
めたオクチル199.9kgを入れ、原料を約40分間攪
拌し、硝酸塩を完全に吸収させた。(Example of a solid composite obtained in a form other than a tablet) Example D Method for producing a cetane number improver in the form of solid granules (cold method) Duurethane (1, 2,
4,5-tetramethylbenzene) (C 10 H 16 )
1,200 kg and 199.9 kg of octyl, which had been previously dyed blue with 0.1 kg of a fat-soluble blue dye, were added, and the raw materials were stirred for about 40 minutes to completely absorb the nitrates.
小さな青色の鱗片状の顆粒が得られ、14,28%
の硝酸オクチルを含む。ジーゼル燃料20リツトル
を処理する顆粒20gを含むヒートシールされたポ
リエチレン袋を次の既知の方法で製造した。セタ
ン価は、もとのセタン価が47であるジーゼル燃料
において7単位増加した。 Small blue scaly granules are obtained, 14,28%
Contains octyl nitrate. A heat-sealed polyethylene bag containing 20 g of granules for treating 20 liters of diesel fuel was manufactured in the following known manner. The cetane number increased by 7 units in diesel fuel with an original cetane number of 47.
実施例 E
2サイクルエンジンのための顆粒状潤滑化剤の
製法(コールド法)
鋼製の混合機にジフエニルエチレン(C14H12)
800kgを入れ、次いで、ペンタエリスリトールテ
トラオレエート200kgを加え、生成物が完全に吸
着されるまで、約40分間ゆつくりとしたスピード
で攪拌し、顆粒を得た。既知の方法を用い、10g
ずつを含むヒートシールされたポリエチレン袋を
製造した。各々担体8gと潤滑剤2gから成る顆
粒を含む。各袋は、2サイクルエンジンの燃料タ
ンク中に入れて用い、その割合は、燃料1リツト
ル当り1袋であり、過酷なレースにおいて燃料と
の混合物の潤滑性を高めるため、また、低馬力エ
ンジンのオートバイに用いる場合、更に一般の潤
滑剤を加える必要のない十分な潤滑性を燃料に与
えるのに適する。Example E Method for producing granular lubricant for two-stroke engines (cold method) Diphenylethylene (C 14 H 12 ) is added to a steel mixer.
Then, 200 kg of pentaerythritol tetraoleate was added and stirred at a slow speed for about 40 minutes until the product was completely adsorbed to obtain granules. Using known methods, 10g
Heat-sealed polyethylene bags were manufactured containing Each contains granules consisting of 8 g of carrier and 2 g of lubricant. Each bag is placed in the fuel tank of a two-stroke engine, at a ratio of one bag per liter of fuel, to improve the lubricity of the fuel mixture during tough races, and for low horsepower engines. When used in motorcycles, it is suitable for providing sufficient lubricity to the fuel without the need for further addition of conventional lubricants.
該複合体は、下記の特性を有する。 The complex has the following properties.
各錠剤が、計量せずに、燃料の特定リツトル当
りの配合量の添加剤を含有するものであるので、
直接の消費者又は使用者が容易に用いらるもので
ある。 Since each tablet contains an unmetered amount of additive per specified liter of fuel,
It is easily used by the direct consumer or user.
製品の貯蔵上危険なく、容易に貯蔵しうるもの
である。 The product is safe to store and can be easily stored.
市販燃料の比重よりも比重が高いものは、徐々
に溶解しながら、タンクの底部に落下して、タン
クの底部での有効成分の濃度が高くなり、ここ
で、燃料の吸引がおこなわれるので、これらの特
性に関して、強力な化学作用が生じる。 Fuel with a specific gravity higher than that of commercially available fuel gradually dissolves and falls to the bottom of the tank, increasing the concentration of active ingredients at the bottom of the tank, where the fuel is sucked. With these properties, a powerful chemistry occurs.
用いられる製品に関して、下記の効果が得られ
る。 Regarding the products used, the following effects can be obtained.
第1、オツトサイクルエンジン 燃料の浄化、(浄化作用)。1st, Otsutocycle engine Fuel purification (purification effect).
エンジン、特に、P.C.V.バブル中の浄化の改善
(分散作用)。 Improved purification (dispersion action) in the engine, especially in the PCV bubble.
燃料中の氷の生成の低減(抗氷作用)。 Reduction of ice formation in fuel (anti-icing effect).
タンク及びガソリン供給部の防錆性及び防蝕
性。 Rust and corrosion resistance of tanks and gasoline supply parts.
汚染物たとえば、酸炭素類、未燃炭化水素類の
生成の減少。 Reduced production of pollutants such as acid carbons and unburned hydrocarbons.
第2、ヂーゼルサイクルエンジン セタン価の増加。Second, diesel cycle engine Increase in cetane number.
発煙性の低下。 Reduced smoke production.
インジエクターの浄化。 Cleaning the injector.
タンク及びヂーゼル油供給分の防蝕性及び防錆
性。 Corrosion and rust prevention properties of tanks and diesel oil supplies.
インジエクシヨンシステムの管理時間間隔の延
長。 Extended management time interval for injection system.
エンジン効率の増加。 Increased engine efficiency.
寒冷時のスタートの容易性。 Ease of starting in cold weather.
錠剤態の製品は、その保存安定性を与え、取扱
いを容易にするために、ヒートシール包装して販
売しうるし、又、箱、その他適当な容器に入れて
販売しうる。 Products in tablet form may be sold in heat-sealed packaging or in boxes or other suitable containers to provide storage stability and ease of handling.
Claims (1)
素系担体に担持した複合体であつて、該複合体
は、液状炭化水素類に可溶性である燃料用添加剤
の複合体。 2 担体の炭化水素が、少なくとも17炭素原子を
有する組成の脂肪族炭化水素類から選択されたも
のである特許請求の範囲第1項記載の複合体。 3 担体の炭化水素が、少なくとも12炭素原子を
有する組成の脂環式炭化水素類から選択されたも
のである特許請求の範囲第1項記載の複合体。 4 担体の炭化水素が、少なくとも10炭素原子を
有する芳香族炭化水素類から選択されたものであ
る特許請求の範囲第1項記載の複合体。 5 担体が、ナフタレンを含有するものである特
許請求の範囲第1項記載の複合体。 6 複合体が、錠剤である特許請求の範囲第1、
2、3、4又は5項記載の複合体。 7 公知の燃料添加剤を特許請求の範囲第2、
3、4又は5項記載の担体に吸収させ、錠剤とし
た特許請求の範囲第6項記載の複合体。[Scope of Claims] 1. A composite in which a fuel additive for internal combustion engines is supported on a hydrocarbon carrier that is solid at room temperature, the composite being a composite of a fuel additive that is soluble in liquid hydrocarbons. body. 2. The composite according to claim 1, wherein the hydrocarbon of the carrier is selected from aliphatic hydrocarbons having a composition having at least 17 carbon atoms. 3. The composite according to claim 1, wherein the hydrocarbon of the carrier is selected from alicyclic hydrocarbons having a composition having at least 12 carbon atoms. 4. The composite according to claim 1, wherein the hydrocarbon of the carrier is selected from aromatic hydrocarbons having at least 10 carbon atoms. 5. The composite according to claim 1, wherein the carrier contains naphthalene. 6 Claim 1, wherein the complex is a tablet;
The complex according to item 2, 3, 4 or 5. 7. Known fuel additives in claim 2,
6. The complex according to claim 6, which is absorbed into the carrier according to claim 3, 4 or 5 and made into a tablet.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT8020113A IT1206306B (en) | 1980-02-22 | 1980-02-22 | SOLID COMPLEX WITH FUEL ADDITIVE. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56118492A JPS56118492A (en) | 1981-09-17 |
| JPH0229712B2 true JPH0229712B2 (en) | 1990-07-02 |
Family
ID=11163898
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62481A Granted JPS56118492A (en) | 1980-02-22 | 1981-01-06 | Composite body of fuel additive |
Country Status (26)
| Country | Link |
|---|---|
| JP (1) | JPS56118492A (en) |
| AT (1) | AT373619B (en) |
| AU (1) | AU6516980A (en) |
| BE (1) | BE886398A (en) |
| BR (1) | BR8008620A (en) |
| CA (1) | CA1134616A (en) |
| CH (1) | CH645402A5 (en) |
| DD (1) | DD155904A5 (en) |
| DE (1) | DE3044103A1 (en) |
| DK (1) | DK530180A (en) |
| ES (1) | ES499337A0 (en) |
| FI (1) | FI74300C (en) |
| FR (1) | FR2476673B1 (en) |
| GB (1) | GB2079783B (en) |
| GR (1) | GR70227B (en) |
| IE (1) | IE50589B1 (en) |
| IL (1) | IL61632A0 (en) |
| IT (1) | IT1206306B (en) |
| LU (1) | LU82969A1 (en) |
| NL (1) | NL8007027A (en) |
| NO (1) | NO151160C (en) |
| NZ (1) | NZ195826A (en) |
| PL (1) | PL228840A1 (en) |
| PT (1) | PT71800B (en) |
| SE (1) | SE8008403L (en) |
| ZA (1) | ZA807518B (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4639255A (en) * | 1980-01-15 | 1987-01-27 | Phillips Petroleum Company | Solid form additives and method of forming same |
| IT1156129B (en) * | 1982-12-02 | 1987-01-28 | Anic Spa | CHEMICAL COMPOUNDS TO BE USED AS SOLID SUPPORTS OF FUEL ADDITIVES |
| FR2557587B1 (en) * | 1984-01-04 | 1986-10-17 | Polaroil Sa | HYDROCARBON ADDITIVE, PROCESS FOR THEIR PREPARATION, USE FOR LOWERING THE LIMIT TEMPERATURE OF FILTERABILITY OF FUELOILS AND GASOILS |
| GB2214517A (en) * | 1988-01-27 | 1989-09-06 | Exxon Chemical Patents Inc | Carrier for additives for liquid hydrocarbons |
| DE19804756A1 (en) | 1998-02-06 | 1999-08-12 | Basf Ag | Solid fuel additives |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB539285A (en) * | 1940-03-08 | 1941-09-03 | Stanley Ben Grundy | Improvements in and relating to chemical preparations for addition to motor spirit |
| GB795929A (en) * | 1954-08-05 | 1958-06-04 | Ethyl Corp | Method of increasing the cetane number of a compression ignition engine fuel |
| FR1402907A (en) * | 1964-03-12 | 1965-06-18 | Integral powder decalaminant | |
| FR1468882A (en) * | 1965-11-03 | 1967-02-10 | Liem Ets | Process for adding chemical compounds to fuels or liquid fuels |
| US3781171A (en) * | 1971-09-24 | 1973-12-25 | G Maccaferri | Additive composition for the combustion air in internal combustion engines |
| GB1455250A (en) * | 1972-12-13 | 1976-11-10 | Century Oils Ltd | Corrosion inhibitng preparations |
-
1980
- 1980-02-22 IT IT8020113A patent/IT1206306B/en active
- 1980-08-13 FR FR8018084A patent/FR2476673B1/en not_active Expired
- 1980-08-19 GB GB8026970A patent/GB2079783B/en not_active Expired
- 1980-09-11 CA CA000360123A patent/CA1134616A/en not_active Expired
- 1980-09-12 PT PT71800A patent/PT71800B/en unknown
- 1980-11-24 DE DE19803044103 patent/DE3044103A1/en active Granted
- 1980-11-28 BE BE0/202969A patent/BE886398A/en not_active IP Right Cessation
- 1980-11-28 LU LU82969A patent/LU82969A1/en unknown
- 1980-12-01 SE SE8008403A patent/SE8008403L/en not_active Application Discontinuation
- 1980-12-02 ZA ZA00807518A patent/ZA807518B/en unknown
- 1980-12-04 FI FI803783A patent/FI74300C/en not_active IP Right Cessation
- 1980-12-04 IL IL61632A patent/IL61632A0/en unknown
- 1980-12-04 CH CH897180A patent/CH645402A5/en not_active IP Right Cessation
- 1980-12-08 AU AU65169/80A patent/AU6516980A/en not_active Abandoned
- 1980-12-12 DK DK530180A patent/DK530180A/en not_active Application Discontinuation
- 1980-12-12 AT AT0604080A patent/AT373619B/en not_active IP Right Cessation
- 1980-12-15 NZ NZ195826A patent/NZ195826A/en unknown
- 1980-12-19 GR GR63724A patent/GR70227B/el unknown
- 1980-12-22 IE IE2701/80A patent/IE50589B1/en unknown
- 1980-12-24 NL NL8007027A patent/NL8007027A/en not_active Application Discontinuation
- 1980-12-29 NO NO803948A patent/NO151160C/en unknown
- 1980-12-30 PL PL22884080A patent/PL228840A1/xx unknown
- 1980-12-30 DD DD80226725A patent/DD155904A5/en unknown
- 1980-12-30 BR BR8008620A patent/BR8008620A/en unknown
-
1981
- 1981-01-06 JP JP62481A patent/JPS56118492A/en active Granted
- 1981-02-11 ES ES499337A patent/ES499337A0/en active Granted
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2233091C (en) | High molecular weight fuel additive | |
| NO20151161L (en) | Fuel and fuel additive formulation | |
| AU648564B2 (en) | Motor fuels of enhanced properties | |
| US5055625A (en) | Gasoline additive composition and method for using same | |
| JPH0229712B2 (en) | ||
| US3925031A (en) | Fuel and oil additive | |
| CN101418241A (en) | Methanol gasoline fuel | |
| CN101294109A (en) | Alcohol ether fuel for diesel of vehicle and marine, and gas-liquid synthesizing method | |
| CH645401A5 (en) | METHOD FOR PRODUCING DESULFURED COOKED FOR ANODES USED IN ALUMINUM ELECTROLYSIS. | |
| US4682984A (en) | Diesel fuel additive | |
| CA2319526A1 (en) | Solid fuel additive | |
| Carter et al. | How to make biodiesel | |
| FR2537153A1 (en) | CHEMICAL COMPOUNDS FOR USE AS SOLID VEHICLES FOR FUEL ADDITIVES | |
| US5147413A (en) | Methanol fuel containing flame luminosity agent | |
| CA1141544A (en) | 1, 1-diethoxyethane as diesel fuel | |
| CN108753383A (en) | A kind of application of fuel assistants and preparation method thereof and the fuel assistants | |
| GB2237027A (en) | Solid ester lubricant | |
| CN105419886A (en) | Compound fuel and preparation method and application thereof | |
| Albright et al. | Utilization of 2, 2-Dinitropropane as a Cetane Number Improved | |
| JPH04213391A (en) | Additive for diesel fuel | |
| JP2003501513A (en) | Gasoline composition | |
| CN102433175A (en) | Diesel flow improver composition | |
| WO2014160802A1 (en) | Fuel additive and fuel composition | |
| CN1032185A (en) | Diesel-dope and production method thereof | |
| CN102433176A (en) | Diesel flow improver composition |