JPH0235000B2 - - Google Patents
Info
- Publication number
- JPH0235000B2 JPH0235000B2 JP58106663A JP10666383A JPH0235000B2 JP H0235000 B2 JPH0235000 B2 JP H0235000B2 JP 58106663 A JP58106663 A JP 58106663A JP 10666383 A JP10666383 A JP 10666383A JP H0235000 B2 JPH0235000 B2 JP H0235000B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- formula
- carbon atoms
- hydrocarbon
- general formula
- 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
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 13
- 239000000446 fuel Substances 0.000 claims description 10
- 125000003277 amino group Chemical group 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims 1
- -1 methylcarbamoyl group Chemical group 0.000 description 12
- 239000007789 gas Substances 0.000 description 11
- 239000013618 particulate matter Substances 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000000779 smoke Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000009835 boiling Methods 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
Description
本発明はデイーゼルエンジン用燃料組成物に関
し、詳しくは軽油に特定のポリオキシアルキレン
化合物を必須成分として添加してなる、排気ガス
中のHC、CO濃度およびパテイキユレートが著し
く減少するデイーゼルエンジン用燃料組成物に関
する。
現在、我国のデイーゼルエンジンの排気ガスに
ついては、HC、CO、NO、黒煙の排出量がそれ
ぞれ規制されている。それに対して米国では小型
デイーゼルエンジンについてはこれらの代わりに
パテイキユレートの排出重量で規制されている。
なお、このパテイキユレートとは排気ガス中に
含まれる微粒子のことであり、その大部分はカー
ボン粒子であるが、燃料の部分燃焼によつて生成
する比較的高沸点の炭化水素成分も含まれるた
め、パテイキユレート低減対策は同時に黒煙、
HC濃度低減対策とも関連する重要なものであ
る。
パテイキユレート低減対策としては、単に黒煙
低減対策やHC低減対策では不十分であり、現
在、排気管途中にセラミツクなどのフイルターを
とりつけてパテイキユレートを補集する方法が考
案されている。しかしながらこの方法は運転を続
けるとフイルターにパテイキユレートが蓄積して
つまり、背圧が増大するという欠点がある。また
この蓄積したすすを触媒やバーナーなどで自動的
に燃焼させる装置が開発されつつあるが、制御機
構が非常に困難であり、さらにそれに伴なう重量
増加、コスト上昇などの問題がある。したがつて
パテイキユレートの低減対策について、容易でか
つコストのあまりかからない方法が求められてい
た。
本発明者らはこのパテイキユレート低減対策に
着目し、容易でかつコストをあまりかけずにパテ
イキユレートを減少させる方法を発明すべく研究
を重ねた結果、軽油の特定のポレオキシアルキレ
ン化合物を必須成分として添加したものをデイー
ゼルエンジン用燃料として使用することにより、
排気ガス中のパテイキユレートだけでなく、同時
にCO濃度やHC濃度も著しく低減できることを見
い出し、本発明を完成するに至つた。
本発明は、軽油に一般式
The present invention relates to a fuel composition for a diesel engine, and more particularly, a fuel composition for a diesel engine, which is made by adding a specific polyoxyalkylene compound to light oil as an essential component, and which significantly reduces HC and CO concentrations and particulate matter in exhaust gas. Regarding. Currently, regarding exhaust gas from diesel engines in Japan, the emissions of HC, CO, NO, and black smoke are regulated. In contrast, in the United States, small diesel engines are regulated based on the exhaust weight of particulate matter instead. Note that particulates are fine particles contained in exhaust gas, most of which are carbon particles, but they also contain hydrocarbon components with relatively high boiling points produced by partial combustion of fuel. Measures to reduce particulate matter also reduce black smoke.
This is an important issue related to measures to reduce HC concentration. Mere measures to reduce black smoke and HC are not sufficient to reduce particulate matter, and currently a method has been devised to collect particulate matter by installing a ceramic filter in the middle of the exhaust pipe. However, this method has the disadvantage that particulate accumulates in the filter as the filter continues to operate, resulting in increased back pressure. Additionally, devices are being developed that automatically burn this accumulated soot using catalysts, burners, etc., but the control mechanism is extremely difficult, and there are additional problems such as increased weight and cost. Therefore, there has been a need for an easy and inexpensive method for reducing particulate matter. The inventors of the present invention focused on this measure to reduce particulate matter, and as a result of repeated research to invent a method to reduce particulate matter easily and without much cost, the inventors added a specific polyoxyalkylene compound of light oil as an essential component. By using this as fuel for diesel engines,
The inventors discovered that not only the particulate matter in exhaust gas but also the CO concentration and HC concentration can be significantly reduced, leading to the completion of the present invention. The present invention applies the general formula to light oil.
【式】または[expression] or
【式】
〔式中、R1は1〜10個の炭素原子を含有する炭
化水素基の1〜2個の水素原子がヒドロキシル基
および/またはアミノ基で置換された基、一般式
[Formula] [In the formula, R 1 is a group in which 1 to 2 hydrogen atoms of a hydrocarbon group containing 1 to 10 carbon atoms are substituted with a hydroxyl group and/or an amino group, general formula
【式】(式中R4は1〜9個の炭素原子を含有
する炭化水素基の1〜2個の水素原子がヒドロキ
シル基および/またはアミノ基で置換された基を
示す)で表わされる基、および一般式
[Formula] (wherein R 4 represents a group in which 1 to 2 hydrogen atoms of a hydrocarbon group containing 1 to 9 carbon atoms are substituted with a hydroxyl group and/or an amino group) , and the general expression
【式】(式中、R5は1〜9個の炭素原
子を含有する炭化水素基、またはこの炭化水素基
の1〜2個の水素原子がヒドロキシル基および/
またはアミノ基で置換された炭化水素基を示す)
で表わされる基よりなる群から選ばれる基、R2
は炭素数2〜5のアルキル基、R3は炭素数1〜
30の炭化水素基およびnは5〜40の整数をそれぞ
れ示す〕で表わされる平均分子量400〜6000のポ
リオキシアルキレン化合物を必須成分として0.05
〜5重量%添加添加してなるデイーゼルエンジン
用燃料組成物を提供するものである。
以下、本発明の内容をより詳細に説明する。
本発明でいう軽油とは、デイーゼルエンジンの
燃料として使用される石油留分でたとえば沸点範
囲が約190〜380℃の油であり、JISK2204に規定
されている1〜3号軽油などが代表的なものであ
る。
また本発明でいうポリオキシアルキレン化合物
とは一般式
で表わされる平均分子量400〜6000、好ましくは
700〜3000の化合物である。
(1)式中でR1は1〜10の炭素原子を含有する炭
化水素基の1〜2個の水素原子がヒドロキシル基
および/またはアミノ基で置換された基、一般式
[Formula] (wherein R 5 is a hydrocarbon group containing 1 to 9 carbon atoms, or 1 to 2 hydrogen atoms of this hydrocarbon group are hydroxyl groups and/or
or a hydrocarbon group substituted with an amino group)
A group selected from the group consisting of the groups represented by R 2
is an alkyl group having 2 to 5 carbon atoms, and R 3 is an alkyl group having 1 to 5 carbon atoms.
30 hydrocarbon groups and n is an integer of 5 to 40, respectively] with an average molecular weight of 400 to 6000 as an essential component and 0.05
The present invention provides a fuel composition for a diesel engine, in which an amount of ~5% by weight is added. Hereinafter, the content of the present invention will be explained in more detail. The term "light oil" as used in the present invention refers to a petroleum fraction used as fuel for diesel engines, for example, with a boiling point range of approximately 190 to 380 degrees Celsius, and typical examples include No. 1 to 3 light oil as specified in JISK2204. It is something. In addition, the polyoxyalkylene compound referred to in the present invention has the general formula Average molecular weight expressed by 400 to 6000, preferably
700-3000 compounds. (1) In the formula, R 1 is a hydrocarbon group containing 1 to 10 carbon atoms in which 1 to 2 hydrogen atoms are substituted with a hydroxyl group and/or an amino group, general formula
【式】(式中、R4は1〜9個の炭素原子を含
有する炭化水素基の1〜2個の水素原子がヒドロ
キシル基および/またはアミノ基で置換された基
を示す)で表わされる基、および一般式
[Formula] (wherein R 4 represents a group in which 1 to 2 hydrogen atoms of a hydrocarbon group containing 1 to 9 carbon atoms are substituted with a hydroxyl group and/or an amino group) groups, and general formulas
【式】(式中、R5は1〜9個の炭素原
子を含有する炭化水素基、またはこの炭化水素基
の1〜2個の水素原子がヒドロキシル基および/
またはアミノ基で置換された炭化水素基を示す)
で表わされる基よりなる群から選ばれる基を示し
ている。ここでいう炭化水素基としては、たとえ
ばアルキル基、アルケニル基、シクロアルキル
基、アルキルシクロアルキル基、アリール基、ア
ルキルアリール基、アラルキル基などがあげられ
る。
本発明でR1としては、一般式[Formula] (wherein R 5 is a hydrocarbon group containing 1 to 9 carbon atoms, or 1 to 2 hydrogen atoms of this hydrocarbon group are hydroxyl groups and/or
or a hydrocarbon group substituted with an amino group)
Indicates a group selected from the group consisting of the groups represented by. Examples of the hydrocarbon group here include an alkyl group, an alkenyl group, a cycloalkyl group, an alkylcycloalkyl group, an aryl group, an alkylaryl group, and an aralkyl group. In the present invention, R 1 is represented by the general formula
【式】で表わ される基、一般式Represented by [formula] group, general formula
【式】で表わされる
基が好ましい。
具体的にはたとえば、メチルカルバモイル基、
エチルカルバモイル基、プロピルカルバモイル
基、ブチルカルバモイル基、ペンチルカルバモイ
ル基、ヘキシルカルバモイル基、ヘプチルカルバ
モイル基、オクチルカルバモイル基、ノニルカル
バモイル基、デシルカルバモイル基、シクロヘキ
シルカルバモイル基、フエニルカルバモイル基お
よび一般式
〔式中、R6は炭素数2〜4のアルキレン基を示
す〕で表わされる基などがあげられる。
本発明においてR1として特に好ましいのは上
記一般式A group represented by the formula is preferred. Specifically, for example, methylcarbamoyl group,
Ethylcarbamoyl group, propylcarbamoyl group, butylcarbamoyl group, pentylcarbamoyl group, hexylcarbamoyl group, heptylcarbamoyl group, octylcarbamoyl group, nonylcarbamoyl group, decylcarbamoyl group, cyclohexylcarbamoyl group, phenylcarbamoyl group and general formula Examples include a group represented by [wherein R 6 represents an alkylene group having 2 to 4 carbon atoms]. In the present invention, the above general formula is particularly preferable as R 1
燃料組成物を用いて排気量1800c.c.のデイーゼル
エンジンを動かし、車速30Km/hrでのダイナモ出
力2.0、4.0、6.0psおよび車速50Km/hrでのダイナ
モ出力6.0、8.0、10.0psの際の排気ガス中のHC濃
度、CO濃度およびパテイキユレート量を測定し
た。ただしHC濃度、CO濃度およびパテイキユレ
ート量の測定は次の方法によつた。
●HC濃度およびCO濃度
デイーゼルエンジンを90分間暖気運転後、排
気ガスをダイリユーシヨントンネルに導き、一
定のエンジン回転速度およびトルク条件で5分
間バツグに排気ガスを採取した。このガスを
Federal Register VOL.45、No.45(March
5、1980)の40 CFR PART86に記載の方法
に準処して分析し、濃度を求めた。
●パテイキユレート量
上記と同様の条件で2〜5分間フイルターに
排気ガスを通し、パテイキユレートを採取し
た。このフイルターを恒温(25℃)、恒湿(60
%)下で18時間保持した後、マイクロ天秤で重
量を測定し、フイルター重量を差し引くことに
より求めた。
実施例2〜5および比較例
JIS2号軽油に次式で表わされるポリオキシアル
キレン化合物(実施例2〜5)をそれぞれ1重量
%添加して本発明の組成物を得た。
これらの燃料組成物について、実施例1と同様
の性能評価試験を行つた結果を第1表および第2
表に示した。
また比較のため、これらポリオキシアルキレン
化合物を添加せずに2号軽油だけを用いて同様の
性能評価試験を行い、その結果も第1表および第
2表に併記した。
第1表および第2表の結果から、本発明の燃料
組成物はポリオキシアルキレン化合物を添加して
いない軽油に比べ、排気ガス中のHC濃度、CO濃
度およびパテイキユレート量が著しく減少してお
り、その優秀性が明らかである。
Using the fuel composition to operate a diesel engine with a displacement of 1800 c.c., the dynamo outputs were 2.0, 4.0, and 6.0 ps at a vehicle speed of 30 km/hr, and the dynamo outputs were 6.0, 8.0, and 10.0 ps at a vehicle speed of 50 km/hr. The HC concentration, CO concentration, and particulate amount in the exhaust gas were measured. However, the measurement of HC concentration, CO concentration, and particulate amount was carried out by the following method. ●HC concentration and CO concentration After the diesel engine was warmed up for 90 minutes, the exhaust gas was introduced into the dilution tunnel, and the exhaust gas was sampled for 5 minutes at a constant engine speed and torque condition. this gas
Federal Register VOL.45, No.45 (March
The concentration was determined by analysis according to the method described in 40 CFR PART 86 of 5, 1980). ●Amount of particulate matter Exhaust gas was passed through the filter for 2 to 5 minutes under the same conditions as above, and particulate matter was collected. This filter is kept at constant temperature (25℃) and constant humidity (60℃).
%) for 18 hours, the weight was determined using a microbalance and the weight of the filter was subtracted. Examples 2 to 5 and Comparative Example Compositions of the present invention were obtained by adding 1% by weight of each of polyoxyalkylene compounds (Examples 2 to 5) represented by the following formulas to JIS No. 2 gas oil. Tables 1 and 2 show the results of the same performance evaluation tests as in Example 1 for these fuel compositions.
Shown in the table. For comparison, a similar performance evaluation test was conducted using only No. 2 diesel oil without adding these polyoxyalkylene compounds, and the results are also listed in Tables 1 and 2. From the results in Tables 1 and 2, the fuel composition of the present invention has significantly reduced HC concentration, CO concentration, and particulate amount in exhaust gas, compared to light oil to which no polyoxyalkylene compound is added. Its excellence is clear.
【表】【table】
Claims (1)
【式】または 【式】(式中、R1は1 〜10個の炭素原子を含有する炭化水素基の1〜2
個の水素原子がヒドロキシル基および/またはア
ミノ基で置換された基、一般式【式】(式 中、R4は1〜9個の炭素原子を含有する炭化水
素基の1〜2個の水素原子がヒドロキシル基およ
び/またはアミノ基で置換された基を示す)で表
わされる基、および一般式【式】(式 中、R5は1〜9個の炭素原子を含有する炭化水
素基、またはこの炭化水素基の1〜2個の水素原
子がヒドロキシル基および/またはアミノ基で置
換された炭化水素基を示す)で表わされる基より
なる群から選ばれる基、R2は炭素数2〜5のア
ルキル基、R3は炭素数1〜30の炭化水素基、そ
してnは5〜40の整数をそれぞれ示す〕で表わさ
れる平均分子量400〜6000のポリオキシアルキレ
ン化合物を必須成分として0.05〜5重量%添加し
てなるデイーゼルエンジン用燃料組成物。[Scope of Claims] 1 Light oil has the general formula [Formula] or [Formula] (wherein R 1 is 1 to 2 hydrocarbon groups containing 1 to 10 carbon atoms)
A group in which 1 to 2 hydrogen atoms are substituted with a hydroxyl group and/or an amino group, with the general formula (representing a group in which an atom is substituted with a hydroxyl group and/or an amino group), and a group represented by the general formula [Formula] (wherein R 5 is a hydrocarbon group containing 1 to 9 carbon atoms, or A group selected from the group consisting of a hydrocarbon group in which 1 to 2 hydrogen atoms of the hydrocarbon group are substituted with a hydroxyl group and/or an amino group, R 2 is a group having 2 to 5 carbon atoms. R 3 is a hydrocarbon group having 1 to 30 carbon atoms, and n is an integer of 5 to 40], and has an average molecular weight of 400 to 6000 as an essential component. A diesel engine fuel composition containing %.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10666383A JPS59232176A (en) | 1983-06-16 | 1983-06-16 | Fuel composition for diesel engine |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10666383A JPS59232176A (en) | 1983-06-16 | 1983-06-16 | Fuel composition for diesel engine |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59232176A JPS59232176A (en) | 1984-12-26 |
JPH0235000B2 true JPH0235000B2 (en) | 1990-08-07 |
Family
ID=14439319
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10666383A Granted JPS59232176A (en) | 1983-06-16 | 1983-06-16 | Fuel composition for diesel engine |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59232176A (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4778481A (en) * | 1983-08-08 | 1988-10-18 | Chevron Research Company | Diesel fuel and method for deposit control in compression ignition engines |
US5425790A (en) * | 1992-12-23 | 1995-06-20 | Arco Chemical Technology, L.P. | Diesel fuel |
US5314511A (en) * | 1992-12-23 | 1994-05-24 | Arco Chemical Technology, L.P. | Diesel fuel |
JP3560173B2 (en) * | 1993-04-05 | 2004-09-02 | 株式会社ジョモテクニカルリサーチセンター | Fuel composition for diesel engine |
US5308365A (en) * | 1993-08-31 | 1994-05-03 | Arco Chemical Technology, L.P. | Diesel fuel |
DK0946684T3 (en) * | 1996-12-20 | 2005-06-20 | Shell Int Research | Use of diesel fuel additives |
DE102008032254B4 (en) * | 2008-07-09 | 2010-10-21 | Man Nutzfahrzeuge Ag | Low-carbon diesel fuels containing a fuel additive, their use and the use of the fuel additive for the production of low-carbon diesel fuels |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57177092A (en) * | 1981-03-31 | 1982-10-30 | Exxon Research Engineering Co | Glycol ester flow improving additive for distilled fuel |
-
1983
- 1983-06-16 JP JP10666383A patent/JPS59232176A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57177092A (en) * | 1981-03-31 | 1982-10-30 | Exxon Research Engineering Co | Glycol ester flow improving additive for distilled fuel |
Also Published As
Publication number | Publication date |
---|---|
JPS59232176A (en) | 1984-12-26 |
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