JPS6026089A - Carbonaceous fuel oil - Google Patents

Carbonaceous fuel oil

Info

Publication number
JPS6026089A
JPS6026089A JP13408683A JP13408683A JPS6026089A JP S6026089 A JPS6026089 A JP S6026089A JP 13408683 A JP13408683 A JP 13408683A JP 13408683 A JP13408683 A JP 13408683A JP S6026089 A JPS6026089 A JP S6026089A
Authority
JP
Japan
Prior art keywords
surfactant
oil
fuel oil
carbonaceous fuel
present
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
Application number
JP13408683A
Other languages
Japanese (ja)
Inventor
Sugako Ootake
大嶽 崇雅子
Hitoshi Iwata
仁 岩田
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.)
Tokai Rika Co Ltd
Original Assignee
Tokai Rika Co Ltd
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 Tokai Rika Co Ltd filed Critical Tokai Rika Co Ltd
Priority to JP13408683A priority Critical patent/JPS6026089A/en
Priority to GB08421567A priority patent/GB2150241B/en
Priority to AU32490/84A priority patent/AU574380B2/en
Publication of JPS6026089A publication Critical patent/JPS6026089A/en
Pending legal-status Critical Current

Links

Landscapes

  • Liquid Carbonaceous Fuels (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)

Abstract

PURPOSE:To improve the storability of a carbonaceous fuel oil and prevent the deposition of carbides effectively, by adding a surfactant in which a residue of org. phosphonic acid forms a hydrophilic segment, to the carbonaceous fuel oil. CONSTITUTION:A surfactant in which a residue of org. phosphonic acid forms a hydrophilic segment is added to a carbonaceous fuel oil. The surfactant are, e.g., glycerophosphonolipid of formula I (where R1 is a polar group-contg. hydrocarbon; R2 and R3 are long chain hydrocarbons; A is methylene or carbonyl) and sphingophosphonolipid of formula II (where R4 is a long-chain hydrocarbon). The base oil for the fuel oil includes gasoline, gas oil, mixed heavy oil, liquefied petroleum gas, and synthetic diester oil. The surfactant is used in an amt. of 0.01-5.0%. When the amt. is less than 0.01%, no effect is obtained, while when it exceeds 5.0%, the cost becomes too high.

Description

【発明の詳細な説明】 本発明は炭化物の機器への付着を防止する燃料油に関す
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a fuel oil that prevents carbide from adhering to equipment.

自動車用燃料等の燃料油は高温、過熱条件下で使用され
る。このような条件下では、燃料油の主成分である炭素
質のものが炭化し、炭化物が燃料の流入路や摺動部に付
着し、これらが焼き付きをおこしたりして使用機器の損
耗を早めている。
Fuel oil such as automobile fuel is used at high temperatures and under superheated conditions. Under these conditions, the carbonaceous material that is the main component of fuel oil carbonizes, and the carbide adheres to the fuel inflow path and sliding parts, causing seizure and accelerating wear and tear on the equipment used. ing.

特公昭31−10783号公報には、C−〇−P結合を
持った正リン酸残基を親木基1こもっ界面活性剤を自動
車用ガソリンに添加して気化器の堆積物を除去すること
が開示されている。しかしなか呟この界面活性剤は有効
に炭化物のイ」着を防止するものの保存安定性か悪く、
長期間に変色や変質を起こすものである。
Japanese Patent Publication No. 31-10783 discloses that a surfactant containing an orthophosphoric acid residue having a C-〇-P bond is added to automobile gasoline to remove vaporizer deposits. is disclosed. However, although this surfactant effectively prevents the adhesion of carbides, it has poor storage stability.
It causes discoloration and deterioration over a long period of time.

本発明者等は保存安定性か良く、しかも有効に炭化物の
付着を防止する燃料油を得るために鋭意研究の結果、本
発明を成すに到った。即ち、本発明は有機ホスホン酸残
基か親水部を形成する少くとも一種の界面活性剤を含有
する炭素質燃料油に関する。
The present inventors have completed the present invention as a result of intensive research in order to obtain a fuel oil that has good storage stability and effectively prevents the adhesion of carbides. That is, the present invention relates to a carbonaceous fuel oil containing at least one type of surfactant that forms a hydrophilic moiety of organic phosphonic acid residues.

本発明に用いる界面活性剤は有機ホスホン酸残基が親木
部の一部に存在する。このような界面活性剤の代表的な
ものとして次のようなものが挙げられる; CH〜OA R2 Cl]2−〇=A −R、。
In the surfactant used in the present invention, organic phosphonic acid residues are present in a part of the parent xylem. Typical examples of such surfactants include the following: CH~OA R2 Cl]2-〇=A-R.

1式中、R1は極性基を含む炭化水素、R2およびR3
は長鎖炭化水素、Aはメチレン基またはカルボニル基を
表わす。] 1 R1 [式中、R1は極性基を含む炭化水素、R2およびR4
は長鎖炭化水素(R2とR1は異なる)を表わす。] 構造式(1)はグリセロホスホノ糖脂質と呼ばれ、構造
式(2)はスフィンゴホスホバピドと呼ばれている。
In formula 1, R1 is a hydrocarbon containing a polar group, R2 and R3
represents a long-chain hydrocarbon, and A represents a methylene group or a carbonyl group. ] 1 R1 [wherein, R1 is a hydrocarbon containing a polar group, R2 and R4
represents a long chain hydrocarbon (R2 and R1 are different). ] Structural formula (1) is called glycerophosphonoglycolipid, and structural formula (2) is called sphingophosphobapide.

上記界面活性剤中のR1の例としては、化学式%式% られる。R2およびR3の例としては、炭素数12〜1
8の飽和又は不飽和の長鎖炭化水素基が一般的である。
An example of R1 in the above surfactant is the chemical formula %. Examples of R2 and R3 include 12 to 1 carbon atoms;
8 saturated or unsaturated long chain hydrocarbon groups are common.

R1の例としては構造式で  H 1 −C=(>(C112)、2CH3 などの長鎖炭化水素基等が挙げられる。An example of R1 is the structural formula H 1 -C=(>(C112), 2CH3 Examples include long chain hydrocarbon groups such as.

本発明燃料油には、−11記界面活性剤の一種を用いて
もよいが、二種具]−を混合して用いてもよい。
In the fuel oil of the present invention, one type of surfactant listed in -11 may be used, or two types of surfactants may be used in combination.

本発明界面活性剤にはグリセロホスホノ糖脂質。The surfactants of the present invention include glycerophosphonoglycolipids.

スフィンゴホスホノ糖脂質もグリセロホスホノリピド、
スフィンゴホスホノリピFの一種として用いることかで
きる。
Sphingophosphonoglycolipids are also glycerophosphonolipids,
It can be used as a type of sphingophosphonolipi F.

本発明燃料油のベースオイルの例としては、ガソリン、
軽油9重油、又は混炭重油、液化石油ガス、ジエステル
系合成油等がある。
Examples of the base oil of the fuel oil of the present invention include gasoline,
Examples include light oil, 9 heavy oil, mixed coal heavy oil, liquefied petroleum gas, and diester synthetic oil.

本発明に用いる界面活性剤は、ベースオイル中に0.0
1〜5.0重量%、好ましくは0.01〜1.0重量%
含有するのが好ましい。o、 oi重量%以下では本発
明燃料油の効果か達成されない。5.0重量4− %を越えると効果の割に経済的に割高になる。また、容
器や不用のものに付着した場合の洗浄が面倒になったり
、ベースオイルの粘度の低下が著しくなる。
The surfactant used in the present invention is 0.0% in the base oil.
1-5.0% by weight, preferably 0.01-1.0% by weight
It is preferable to contain. If the amount is less than o, oi% by weight, the effect of the fuel oil of the present invention will not be achieved. If it exceeds 5.0% by weight, it becomes economically expensive compared to its effectiveness. Moreover, if it adheres to containers or unnecessary items, cleaning becomes troublesome, and the viscosity of the base oil decreases significantly.

本発明の燃料油を自動車に用いるとガソリン、軽油、液
化石油ガス等の炭素質のベースオイルの炭化物の付着、
焼付けが有効に防止される。
When the fuel oil of the present invention is used in automobiles, adhesion of carbides on carbonaceous base oils such as gasoline, diesel oil, and liquefied petroleum gas;
Burning is effectively prevented.

さらに、本発明の燃料油は極めて保存安定性が良く、変
色および変質の恐れがない。
Furthermore, the fuel oil of the present invention has extremely good storage stability and is free from discoloration and deterioration.

本発明を実施例によりさらに詳細に説明する。The present invention will be explained in more detail with reference to Examples.

実施例中の%は特に指示しない限り、重量%を表わす。% in the examples represents weight % unless otherwise specified.

実施例1〜4 以下の配合量を有する燃料油の炭化物の付着性および保
存安定性を調べた。結果を表−1に示す。
Examples 1 to 4 The adhesion of carbides and storage stability of fuel oils having the following blending amounts were investigated. The results are shown in Table-1.

実施例1の配合量 成 分 % 重 油 75.0 炭 素 粉 24.5 1) 界面活性剤A 0. 5 実施例2の配合量 成 分 % 重 油 75.0 炭 素 粉 24.5 界面活性剤A O,25 2) 界面活性剤B 0025 実施例3の配合量 成 分 % 軽 油 75.0 炭 素 粉 24.5 界面活性剤B 0. 5 実施例4の配合量 成 分 % 軽 油 99.5 界面活性剤B 0. 5 1)第1図に示される赤外吸収スペクトルを有する界面
活性剤。
Blend amount of Example 1 Ingredients % Heavy oil 75.0 Carbon powder 24.5 1) Surfactant A 0. 5 Ingredients blended in Example 2 % Heavy oil 75.0 Carbon powder 24.5 Surfactant A O, 25 2) Surfactant B 0025 Ingredients blended in Example 3 % Light oil 75.0 Charcoal Base powder 24.5 Surfactant B 0. 5 Blend amount of Example 4 Ingredients % Light oil 99.5 Surfactant B 0. 5 1) A surfactant having an infrared absorption spectrum shown in FIG.

2)第2図に示される赤外吸収スペクトルを有する界面
活性剤。
2) A surfactant having an infrared absorption spectrum shown in FIG.

実験」としで、」1記配合処方の燃料油中で固定された
電極に可動電極を用いて50,000回開閉を行った。
In the experiment, a fixed electrode was opened and closed 50,000 times using a movable electrode in fuel oil having the formulation described in 1.

両電極間には12ボルトの電圧をかけ、電流は10アン
ペアであった。この実験でテスト前の接触抵抗、50,
000回開閉後の接触抵抗お上び50,000回開閉後
の電極への炭化物の不着の有無を調べた。
A voltage of 12 volts was applied between the electrodes and the current was 10 amperes. In this experiment, the contact resistance before the test was 50,
The contact resistance after opening and closing 50,000 times and the presence or absence of carbide adhesion to the electrodes after opening and closing 50,000 times were investigated.

実験2として資料200gをガラスビンに入れ、2年問
屋外放置した後の臭いと色の変化を調べた。
In Experiment 2, 200g of the material was placed in a glass bottle and the odor and color changes were examined after it was left outdoors for two years.

比較例1 構造式; %式% を有する正リン酸残基含有グリセロホスホリピドの代表
例として、アセトン精製大豆レシチンを用いて実施例と
同様の試験を行った。配合量は重油75%、炭素粉2.
1.5%、アセトン精製大豆レシチン0.5%であった
。結果を表−1に示す。
Comparative Example 1 As a representative example of an orthophosphoric acid residue-containing glycerophospholipid having the structural formula: % formula %, a test similar to that of the example was conducted using acetone-purified soybean lecithin. The blending amount is 75% heavy oil, 2.
1.5% and acetone-purified soybean lecithin 0.5%. The results are shown in Table-1.

比較例2〜4 界面活性剤を配合しないものを用いて実施例と同様の試
験を行った。配合量を示すと比較例2では重油75%、
炭素粉25%であり、比較例3では重油100%であっ
た。結果を表−1に示す。
Comparative Examples 2 to 4 Tests similar to those in Examples were conducted using products that did not contain a surfactant. In Comparative Example 2, heavy oil was 75%;
The carbon powder was 25%, and in Comparative Example 3, the heavy oil was 100%. The results are shown in Table-1.

(以下、余白) 表−1に示すように、本発明燃料油を電気アークに当て
炭化しても炭化物は自動車用燃料油に分散し電極て゛あ
る金属表面やブラ又チンク表面には11府し難い。また
2年間の屋外放置で・保存安定性に優れていることも解
る。
(Hereinafter, blank spaces) As shown in Table 1, even if the fuel oil of the present invention is carbonized by applying an electric arc, carbides are dispersed in the automotive fuel oil, and 11 particles are formed on the metal surface of the electrode, bra, or tink surface. hard. It can also be seen that it has excellent storage stability after being left outdoors for two years.

一方、比較例1では保存安定性か悪いことか解る。実際
には放置後数日て゛の油の臭の変化と酸化か進行し始め
た。
On the other hand, in Comparative Example 1, it can be seen whether the storage stability is poor or not. In fact, the odor of the oil changed and oxidation began to progress several days after it was left unused.

また、本発明以外の燃料油は炭化物のけ着か顕著に表わ
れ、接触抵抗も、1倍iこ増加した。
In addition, in fuel oils other than those of the present invention, carbide deposition was noticeable, and the contact resistance increased by a factor of 1.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明実施例:こ用いたグリセロホスホ/リピ
ドの赤外線スペクトル、第2図は本発明実施例に用いた
グリセロホスホ/リピド/第1図とは異なる物質の赤外
線吸収スペクトルを示す。 特許出If! /< 株式会社東海理化電磯製作所代 
理 !(弁理士 青 山 葆 :h h= 2名第1図 3500 3001) 2500 2000 +1aω
 16(Xl 1400 1200 1001) 80
0著長Cヶ−7 第2図
FIG. 1 shows an infrared spectrum of glycerophospho/lipid used in an example of the present invention, and FIG. 2 shows an infrared absorption spectrum of glycerophospho/lipid used in an example of the present invention/a substance different from that shown in FIG. If a patent is issued! /< Tokai Rika Deniso Seisakusho Co., Ltd.
Reason! (Patent attorney Aoyama Ao: h h= 2 people Figure 1 3500 3001) 2500 2000 +1aω
16 (Xl 1400 1200 1001) 80
0 length C-7 Figure 2

Claims (1)

【特許請求の範囲】 1、有機ホスホン酸残基が親水部を形成する少くとも一
種の界面活性剤を含有する炭素質燃料油。 2、界面活性剤がグリセロホスホ7リピドである第1項
記載の燃料油。 3、界面活性剤がスフィンゴリピドである第1項記載の
燃料油。 4、界面活性剤をO,Of〜5.0重量%含有する第1
〜3項いずれかに記載の燃料油。
[Claims] 1. A carbonaceous fuel oil containing at least one surfactant in which organic phosphonic acid residues form a hydrophilic part. 2. The fuel oil according to item 1, wherein the surfactant is glycerophospho7lipid. 3. The fuel oil according to item 1, wherein the surfactant is a sphingolipid. 4. The first containing O, Of ~ 5.0% by weight of surfactant
The fuel oil according to any one of items 1 to 3.
JP13408683A 1983-08-30 1983-07-21 Carbonaceous fuel oil Pending JPS6026089A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP13408683A JPS6026089A (en) 1983-08-30 1983-07-21 Carbonaceous fuel oil
GB08421567A GB2150241B (en) 1983-08-30 1984-08-24 Disc brake device automatic adjustment
AU32490/84A AU574380B2 (en) 1983-08-30 1984-08-29 Disc brake slack adjuster

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13408683A JPS6026089A (en) 1983-08-30 1983-07-21 Carbonaceous fuel oil

Publications (1)

Publication Number Publication Date
JPS6026089A true JPS6026089A (en) 1985-02-08

Family

ID=15120083

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13408683A Pending JPS6026089A (en) 1983-08-30 1983-07-21 Carbonaceous fuel oil

Country Status (1)

Country Link
JP (1) JPS6026089A (en)

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