JPS59202293A - Preparation of fuel composition - Google Patents

Preparation of fuel composition

Info

Publication number
JPS59202293A
JPS59202293A JP7598083A JP7598083A JPS59202293A JP S59202293 A JPS59202293 A JP S59202293A JP 7598083 A JP7598083 A JP 7598083A JP 7598083 A JP7598083 A JP 7598083A JP S59202293 A JPS59202293 A JP S59202293A
Authority
JP
Japan
Prior art keywords
alcohol
specific gravity
fuel composition
liquid hydrocarbon
soluble
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
JP7598083A
Other languages
Japanese (ja)
Other versions
JPH0334518B2 (en
Inventor
Kiichi Maruhashi
丸橋 基一
Masayasu Hasegawa
昌康 長谷川
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.)
Nippon Synthetic Chemical Industry Co Ltd
Original Assignee
Nippon Synthetic Chemical Industry 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 Nippon Synthetic Chemical Industry Co Ltd filed Critical Nippon Synthetic Chemical Industry Co Ltd
Priority to JP7598083A priority Critical patent/JPS59202293A/en
Publication of JPS59202293A publication Critical patent/JPS59202293A/en
Publication of JPH0334518B2 publication Critical patent/JPH0334518B2/ja
Granted legal-status Critical Current

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  • Liquid Carbonaceous Fuels (AREA)

Abstract

PURPOSE:To prepare a fuel composition comprising a mixture of liquid hydrocarbon and alcohol which does not cause phase separation even when stored for a long period at a low temperature, by adding a specified alcohol-soluble specific gravity modifier to the alcohol. CONSTITUTION:An alcohol-soluble specific gravity modifier is dissolved in alcohol such as methanol or ethanol to adjust the difference in specific gravity between the alcohol and liquid hydrocarbon (e.g. kerosene, gas oil or heavy fuel oil) to 0.02 or lower. The alcohol is mixed with the liquid hydrocarbon to obtain the aimed fuel composition. The specific gravity modifiers are e.g. ethylene glycol, propylene glycol or polyvinyl acetate. A fuel composition with a higher stability is obtained when the mixing is done in the presence of a small amount of a hydrocarbon-soluble dispersion stabilizer, e.g. polyoxyethylene oleyl ether.

Description

【発明の詳細な説明】 炭化水素系混合物はその混合する化合物の組合せも様々
で燃料用途を代表例としてその用途は多岐にわたってい
る。特に、重質油の燃焼効率を高め軽質油ないし中質油
分野への用途拡大のため、該油中に少量のメタノールを
混合させること等、実用化が期待されている。しかして
、かかる用途においては炭化水素系混合物が相分離をお
こさない様に系を安定に維持するために各種界面活性剤
等の分散安定剤の添加が必要とされている。
DETAILED DESCRIPTION OF THE INVENTION Hydrocarbon mixtures have various combinations of compounds, and their uses are wide-ranging, with fuel being a typical example. In particular, in order to improve the combustion efficiency of heavy oil and expand its application to light oil and medium oil fields, it is expected to be put to practical use, such as by mixing a small amount of methanol into the oil. Therefore, in such applications, it is necessary to add dispersion stabilizers such as various surfactants to maintain the system stably so that the hydrocarbon mixture does not undergo phase separation.

しかしながら該安定剤を使用しても低温時の放置安定性
に劣るため冬場での保存あるいは寒冷地での取扱いにお
いて分散状態が破壊して相分離をおこす恐れがあり、更
に改善の余地がある。
However, even if such a stabilizer is used, the storage stability at low temperatures is poor, and there is a risk that the dispersion state will be destroyed and phase separation will occur during storage in winter or handling in cold regions, and there is still room for further improvement.

しかるに本発明者等はかかる問題を解決するため鋭意研
究を重ねた結果、液状炭化水素とアルコールを混合して
燃料組成物を製造するに当り、アルコール可溶性の比重
調節剤をアルコールに溶解させ液状炭化水素と該アルコ
ールとの比重差を0.025以下に調整する場合、その
目的が達成出来ることを見出し本発明を完成するに到っ
た。
However, as a result of extensive research in order to solve this problem, the present inventors discovered that when producing a fuel composition by mixing liquid hydrocarbon and alcohol, an alcohol-soluble specific gravity regulator is dissolved in alcohol and liquid carbonization is performed. The present invention was completed based on the discovery that the objective can be achieved when the difference in specific gravity between hydrogen and the alcohol is adjusted to 0.025 or less.

液状炭化水素、例えば軽油、A重油、B重油、C重油は
その種類によって多少変動はあるが、通常その比重は0
.85〜0.95程度であり、一方アルコール例えばメ
タノール、エタノール等の比重は0.78〜0.80程
度であり、その比重差はがなり大きく本発明ではアルコ
ールに可溶性の比重調部側をアルコールに添加してその
比重を大きくし、液状炭化水素とアルコールとの比重′
差を0.025以下に調整することにより放置安定性が
改善されるのである。
Liquid hydrocarbons, such as light oil, A heavy oil, B heavy oil, and C heavy oil, usually have a specific gravity of 0, although it varies somewhat depending on the type.
.. On the other hand, the specific gravity of alcohols such as methanol and ethanol is about 0.78 to 0.80, and the difference in specific gravity is large. The specific gravity of liquid hydrocarbon and alcohol is
By adjusting the difference to 0.025 or less, storage stability is improved.

従来、各種の分散安定剤を添加して放置安定性を改善す
ること即ち界面化学的な面での改善が試みられているが
、液状炭化水素とアルコールとの比重を調整しようとす
る技術思想は全く認識されておらず、本発明はかかる従
来の安定化方法とは発想が根本的に相違するのである。
Conventionally, attempts have been made to improve storage stability by adding various dispersion stabilizers, that is, to improve surface chemistry, but the technical idea of adjusting the specific gravity of liquid hydrocarbon and alcohol has not been achieved. This has not been recognized at all, and the concept of the present invention is fundamentally different from such conventional stabilization methods.

本発明で使用する比重調節剤はアルコールに可溶でアシ
、かつ対象とするアルコールより比重の大きい化合物で
あれば特に制限はない。かかる化合物の代表例としては
エチレングリコール、プロピレングリコール、ブチレン
グリコール等のグリコール類が挙げられる。その池、ポ
リ酢酸ビニル、部分グン化ポリ酢酸ビニル、エチレンで
少量共重合変性されたポリ酢酸ビニル及びそのケン化物
、ポリエチレングリコールソルビタンエステル等も使用
可能である1、 かかる調節剤をアルコールに溶解して液状炭化水素とア
ルコールとの比重差を0.025以下、好ましくは0.
002〜θ、θ20の範囲に調節する。
The specific gravity regulator used in the present invention is not particularly limited as long as it is a compound that is soluble in alcohol, has a specific gravity larger than the target alcohol. Representative examples of such compounds include glycols such as ethylene glycol, propylene glycol, and butylene glycol. In addition, polyvinyl acetate, partially gunned polyvinyl acetate, polyvinyl acetate copolymerized with a small amount of ethylene and its saponified product, polyethylene glycol sorbitan ester, etc. can also be used. 1. Dissolve such a regulator in alcohol. The difference in specific gravity between liquid hydrocarbon and alcohol is 0.025 or less, preferably 0.025 or less.
Adjust to a range of 002 to θ, θ20.

0.025以上の比重差では充分な安定化効果が発揮出
来ない。
A sufficient stabilizing effect cannot be exhibited with a specific gravity difference of 0.025 or more.

又、液状炭化水素とアルコールとの混合時に炭化水素に
可溶な分散安定剤を少量共存させることによって一層、
高度の安定性を有する組成物が得られる。
Furthermore, by coexisting a small amount of a dispersion stabilizer soluble in the hydrocarbon when mixing the liquid hydrocarbon and alcohol,
A composition with a high degree of stability is obtained.

かかる安定剤としては例えば少量の酢酸ビニルで共重合
変性されたポリエチレン又はそのケン化物、酢酸ビニル
−α−オレフィン共重合体又はそのケン化物、界面活性
剤等が挙げられる。これらは組成物全体に対して普通0
.01〜5重量%の程度の割合で用いられる。
Examples of such stabilizers include polyethylene copolymerized and modified with a small amount of vinyl acetate or saponified products thereof, vinyl acetate-α-olefin copolymers or saponified products thereof, surfactants, and the like. These are usually 0 for the entire composition.
.. It is used in a proportion of about 0.01 to 5% by weight.

本発明でアルコールとしてはメタノール、が代表的であ
るがエタノール、プロパツール、ブタノール等の高級ア
ルコールも使用可能である。更に液状炭化水素としては
重油、軽油、A重油、B重油、C重油、コールタール、
ピッチ、アスファルトあるいは潤滑油等が例示されるが
、本発明によると特に沸点が200℃以上の炭化水素に
対して顕著な効果が得られる。
In the present invention, methanol is typically used as the alcohol, but higher alcohols such as ethanol, propatool, and butanol can also be used. Furthermore, liquid hydrocarbons include heavy oil, light oil, A heavy oil, B heavy oil, C heavy oil, coal tar,
Examples include pitch, asphalt, lubricating oil, etc., but according to the present invention, remarkable effects can be obtained particularly on hydrocarbons having a boiling point of 200° C. or higher.

液状炭化水素とアルコールとの組成物において実用上か
ら考えて好ましい組合せは、特に軽油/メタノール、重
質油/メタノールあるいはアスファルト/メタノールが
効果が顕著に発揮される。
Preferred combinations of liquid hydrocarbon and alcohol from a practical standpoint are particularly light oil/methanol, heavy oil/methanol, and asphalt/methanol, which are particularly effective.

該混合物における混合比率は特に制限はなく目的に応じ
て任意の範囲から選定すれば良い。例えば重質油にメタ
ノールを混合する場合、実用上60重量%以下のメタノ
ールが使用される。
The mixing ratio in the mixture is not particularly limited and may be selected from any range depending on the purpose. For example, when methanol is mixed with heavy oil, 60% by weight or less of methanol is practically used.

本発明の組成物を調製する際、その混合手段に制限はな
く要は比重調節剤を溶解したアルコール、液状炭化水素
とあるいは好ましくは更に炭化水素に可溶な分散安定剤
を撹拌下に混合しさえすればよい。その添加順序は任意
である。
When preparing the composition of the present invention, there are no restrictions on the mixing means, and the essential thing is to mix alcohol in which a specific gravity adjuster is dissolved, a liquid hydrocarbon, or preferably, a dispersion stabilizer soluble in the hydrocarbon, with stirring. All you have to do is The order of addition is arbitrary.

又かかる操作の際、必要に応じて水、各種界面活性剤、
燃焼助剤等の各種添加剤等任意の化合物の併用も差支え
ない。
Also, during this operation, water, various surfactants,
Any compound such as various additives such as combustion aids may also be used in combination.

かくして得られた組成物は極めて安定性が良好で吐温中
に長期保存しても安定性にすぐれ適度の流動性を有すた
め、燃料に有用である。
The composition thus obtained has extremely good stability, and has excellent stability even when stored for a long period of time at discharge temperature, and has appropriate fluidity, so it is useful as a fuel.

以下、実例を挙げて本発明を更に具体的に説明する。部
又は%とあるのは特にことわりのない限り重量基準であ
る。
Hereinafter, the present invention will be explained in more detail by giving examples. Parts or percentages are by weight unless otherwise specified.

実施例1〜6 液状炭化水素100部を室温下でステンレス容器に仕込
み撹拌下に比重調節剤を溶解したメタノール5部、分散
安定剤を仕込んで組成物を得た。
Examples 1 to 6 100 parts of a liquid hydrocarbon was charged into a stainless steel container at room temperature, and while stirring, 5 parts of methanol in which a specific gravity regulator was dissolved and a dispersion stabilizer were charged to obtain a composition.

この組成物は完全に均一な分散状態であった。該組成物
を室温及び5℃で50日放置しその透過率を測定した。
This composition was completely uniformly dispersed. The composition was left at room temperature and 5° C. for 50 days, and its transmittance was measured.

その結果を第1表に示す。The results are shown in Table 1.

但し、透過率は厚さ2關のセルを用い460mμの波長
にて20℃で測定した。透過率が低い値を示す程均−な
分散状態を呈する。又比重は20℃での測定値である。
However, the transmittance was measured at 20° C. at a wavelength of 460 mμ using a cell with a thickness of 2 mm. The lower the transmittance, the more uniform the dispersion state. Further, the specific gravity is a value measured at 20°C.

Claims (1)

【特許請求の範囲】[Claims] 液状炭化水素とアルコールとを混合して燃料組成物を製
造するに当シ、アルコール可溶性の比重調節剤をアルコ
ールに溶解させ液状炭化水素と該アルコールとの比重差
を0.025以下に調整することを特徴とする燃料組成
物の製造方法。
When producing a fuel composition by mixing a liquid hydrocarbon and alcohol, an alcohol-soluble specific gravity regulator is dissolved in the alcohol to adjust the specific gravity difference between the liquid hydrocarbon and the alcohol to 0.025 or less. A method for producing a fuel composition characterized by:
JP7598083A 1983-04-28 1983-04-28 Preparation of fuel composition Granted JPS59202293A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7598083A JPS59202293A (en) 1983-04-28 1983-04-28 Preparation of fuel composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7598083A JPS59202293A (en) 1983-04-28 1983-04-28 Preparation of fuel composition

Publications (2)

Publication Number Publication Date
JPS59202293A true JPS59202293A (en) 1984-11-16
JPH0334518B2 JPH0334518B2 (en) 1991-05-22

Family

ID=13591910

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7598083A Granted JPS59202293A (en) 1983-04-28 1983-04-28 Preparation of fuel composition

Country Status (1)

Country Link
JP (1) JPS59202293A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05140568A (en) * 1991-11-22 1993-06-08 Yoshihiko Sasao Low-pollution fuel composition
JPH05202373A (en) * 1992-01-29 1993-08-10 Yoshihiko Sasao Low-pollution fuel composition

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HK1194601A2 (en) * 2013-09-04 2014-10-17 威霸玩具 香港 有限公司 A smoke emitting toy

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4930403A (en) * 1972-07-13 1974-03-18
JPS5133128A (en) * 1974-09-13 1976-03-22 Sumitomo Chemical Co
JPS5215602A (en) * 1975-06-17 1977-02-05 Mo Och Domsjoe Ab Control of sulfide value
JPS5532754A (en) * 1978-08-29 1980-03-07 Ichirou Kiji Production of fire* water* sound* and pressure resistant* heat insulating* light weight brick
JPS5611990A (en) * 1979-07-03 1981-02-05 Tomoyasu Noritake Combustion improver for fuel in internal combustion engine

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4930403A (en) * 1972-07-13 1974-03-18
JPS5133128A (en) * 1974-09-13 1976-03-22 Sumitomo Chemical Co
JPS5215602A (en) * 1975-06-17 1977-02-05 Mo Och Domsjoe Ab Control of sulfide value
JPS5532754A (en) * 1978-08-29 1980-03-07 Ichirou Kiji Production of fire* water* sound* and pressure resistant* heat insulating* light weight brick
JPS5611990A (en) * 1979-07-03 1981-02-05 Tomoyasu Noritake Combustion improver for fuel in internal combustion engine

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05140568A (en) * 1991-11-22 1993-06-08 Yoshihiko Sasao Low-pollution fuel composition
JPH0739582B2 (en) * 1991-11-22 1995-05-01 吉彦 篠尾 Low pollution fuel composition
JPH05202373A (en) * 1992-01-29 1993-08-10 Yoshihiko Sasao Low-pollution fuel composition

Also Published As

Publication number Publication date
JPH0334518B2 (en) 1991-05-22

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