JPH0940975A - Fuel oil - Google Patents
Fuel oilInfo
- Publication number
- JPH0940975A JPH0940975A JP19443895A JP19443895A JPH0940975A JP H0940975 A JPH0940975 A JP H0940975A JP 19443895 A JP19443895 A JP 19443895A JP 19443895 A JP19443895 A JP 19443895A JP H0940975 A JPH0940975 A JP H0940975A
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- fuel oil
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- aromatic hydrocarbon
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Abstract
(57)【要約】
【構成】 本発明の燃料油は、軽油留分であって、硫黄
含有量が0.05重量%以下で、かつ2環以上の芳香族
炭化水素の含有量が3.5重量%〜15重量%であり、
該2環以上の芳香族炭化水素中に於ける、炭素数が3個
〜11個の側鎖アルキル基を有する、2環以上の芳香族
炭化水素の占める割合を80重量%以上としたことを特
徴とする。
【効果】 本発明の燃料油は、ディーゼル燃料として、
耐摩耗剤等の添加剤を添加することなく、軽油成分を調
整するだけで耐摩耗性を付与しえるものであり、また、
保存安定性に優れると共に廉価な燃料油である。(57) [Summary] [Constitution] The fuel oil of the present invention is a gas oil fraction having a sulfur content of 0.05% by weight or less and a content of aromatic hydrocarbons of two or more rings of 3. 5% to 15% by weight,
In the aromatic hydrocarbon of two or more rings, the proportion of the aromatic hydrocarbon of two or more rings having a side chain alkyl group having 3 to 11 carbon atoms is 80% by weight or more. Characterize. [Effect] The fuel oil of the present invention is used as a diesel fuel.
Without adding additives such as antiwear agents, it is possible to impart antiwear properties by simply adjusting the gas oil component.
It is a fuel oil that has excellent storage stability and is inexpensive.
Description
【0001】[0001]
【産業上の利用分野】本発明は、低硫黄含有量であると
共に潤滑性に優れたディーゼル用燃料油に関する。TECHNICAL FIELD The present invention relates to a diesel fuel oil having a low sulfur content and excellent lubricity.
【0002】[0002]
【従来の技術】ディーゼルエンジンはガソリンエンジン
に比して燃費が良く、燃料費が安く、しかもエンジンが
丈夫であることから、トラック、バス、船舶、建設機械
等に搭載され、社会環境の変化に伴い、その量は年々増
加の傾向にある。2. Description of the Related Art A diesel engine has better fuel economy than a gasoline engine, has a lower fuel cost, and has a tougher engine. Therefore, it is installed in trucks, buses, ships, construction machinery, etc. As a result, the amount tends to increase year by year.
【0003】しかしながら、軽油(ディーゼル燃料)中
に含有される硫黄は特に重大な社会問題を招き、平成元
年12月に開催された中央公害審議会において、短期目
標として平成4年には軽油における硫黄含有量を0.2
重量%以下とする、また、長期的には平成10年を目途
として0.05重量%以下とすることが諮問され、その
低硫黄化が焦眉の課題となっている。However, sulfur contained in light oil (diesel fuel) poses a particularly serious social problem, and at the Central Pollution Council held in December 1989, a short-term goal for light oil was 1994. Sulfur content 0.2
It has been inquired to set the content to be not more than 10% by weight, and in the long term, to make it not more than 0.05% by weight, aiming at 1998, and its low sulfur content is an urgent issue.
【0004】一般に、軽油中の硫黄の低減は、精製処
理、特に接触水素化により達成されるが、軽油中の硫黄
の低減は、軽油自体の潤滑性の低下を招き、ディーゼル
エンジンのインジェクション装置の損傷を招くという問
題を生じる。特に、硫黄含有量が0.2重量%以下であ
るとインジェクションポンプ(特にロータリーポンプ及
びポンプインジェクター)の摩耗が生じ、その摩耗量
は、硫黄量の低減に応じ比例して増大する。そのため、
例えば脂肪酸エステル等の耐摩耗剤を添加することが知
られているが、これらの添加剤を添加するものは高価で
あったり、また、保存安定性が悪いという問題がある。In general, reduction of sulfur in light oil is achieved by refining treatment, particularly catalytic hydrogenation, but reduction of sulfur in light oil leads to deterioration of lubricity of light oil itself, resulting in deterioration of injection device of diesel engine. It causes a problem of causing damage. In particular, when the sulfur content is 0.2% by weight or less, the injection pump (particularly the rotary pump and the pump injector) is worn, and the wear amount increases in proportion to the decrease in the sulfur amount. for that reason,
For example, it is known to add an antiwear agent such as a fatty acid ester, but those to which these additives are added have the problems of being expensive and having poor storage stability.
【0005】[0005]
【発明が解決しようとする課題】本発明は、耐摩耗剤を
添加しなくても、軽油留分の性状を特定することにより
耐摩耗性に優れた燃料油の提供を課題とする。SUMMARY OF THE INVENTION An object of the present invention is to provide a fuel oil having excellent wear resistance by specifying the properties of a gas oil fraction without adding an antiwear agent.
【0006】[0006]
【課題を解決するための手段】本発明の燃料油は、軽油
留分であって、硫黄含有量が0.05重量%以下で、か
つ2環以上の芳香族炭化水素(以下、多環芳香族炭化水
素という)の含有量が3.5重量%〜15重量%であ
り、該多環芳香族炭化水素中に於ける、炭素数が3個〜
11個の側鎖アルキル基を有する多環芳香族炭化水素
(長鎖アルキル置換多環芳香族炭化水素という)の占め
る割合を80重量%以上としたことを特徴とする。The fuel oil of the present invention is a gas oil fraction, has a sulfur content of 0.05 wt% or less, and is an aromatic hydrocarbon having two or more rings (hereinafter, polycyclic aromatic hydrocarbons). (Referred to as “group hydrocarbon”) is 3.5 wt% to 15 wt%, and the number of carbon atoms in the polycyclic aromatic hydrocarbon is 3 to
It is characterized in that the proportion of polycyclic aromatic hydrocarbons having 11 side chain alkyl groups (referred to as long-chain alkyl-substituted polycyclic aromatic hydrocarbons) is 80% by weight or more.
【0007】本発明の燃料油は、原油、特にはパラフィ
ン系、混合系原油を常圧蒸留し、これを水素化精製して
得られた軽油留分からなり、90%留出点が350℃以
下(沸点、留出点はJIS K 2254に準拠)の蒸
留性状を有し、JIS K2204に規定された軽油の
規格を満足するものである。The fuel oil of the present invention is a gas oil fraction obtained by distilling crude oil, particularly paraffinic and mixed crude oil under atmospheric pressure, and hydrorefining the crude oil. The 90% distillation point is 350 ° C. or lower. It has a distillation property of (boiling point and distilling point according to JIS K 2254) and satisfies the light oil standard defined in JIS K2204.
【0008】本発明の燃料油は、この規格を満足すると
共に、その硫黄含有量を0.05重量%以下とし、かつ
多環芳香族炭化水素の含有量が3.5重量%〜15重量
%であって、該多環芳香族炭化水素中に於ける、長鎖ア
ルキル置換多環芳香族炭化水素の占める割合を80重量
%以上としたものである。The fuel oil of the present invention satisfies this standard and has a sulfur content of 0.05% by weight or less and a polycyclic aromatic hydrocarbon content of 3.5% by weight to 15% by weight. The proportion of the long-chain alkyl-substituted polycyclic aromatic hydrocarbon in the polycyclic aromatic hydrocarbon is 80% by weight or more.
【0009】軽油における芳香族炭化水素含有量は、水
添操作後では、その程度にもよるが、通常、20重量%
〜30重量%であり、その内訳は単環化合物が12重量
%〜27重量%、多環化合物が2重量%〜15重量%で
ある。本発明の燃料油においては、軽油中における多環
芳香族炭化水素の含有量を3.5重量%〜15重量%、
好ましくは3.5重量%〜10重量%とするものであ
る。多環芳香族炭化水素の含有量が15重量%を越える
と、排気ガス中におけるパティキュレートが増大するの
で好ましくなく、また、3.5重量%より少ないと耐摩
耗性に劣る。The content of aromatic hydrocarbons in the light oil is usually 20% by weight after the hydrogenation operation, although it depends on the degree of the content.
-30% by weight, of which 12% to 27% by weight of monocyclic compounds and 2% to 15% by weight of polycyclic compounds. In the fuel oil of the present invention, the content of polycyclic aromatic hydrocarbons in the light oil is 3.5% by weight to 15% by weight,
It is preferably 3.5% by weight to 10% by weight. If the content of polycyclic aromatic hydrocarbons exceeds 15% by weight, the particulate matter in the exhaust gas increases, which is not preferable, and if it is less than 3.5% by weight, the wear resistance is poor.
【0010】置換アルキル基の炭素数毎の分布として
は、5〜7個の側鎖アルキル基を有するものをピーク
(その割合は35重量%〜50重量%)とし、略、正規
分布形状を示し、1〜2個の炭素数の置換アルキル基を
有するものは、置換アルキル基を有する芳香族炭化水素
中、略、5重量%〜15重量%を占める。また、炭素数
12以上のものは、通常の軽油中にほとんど存在しな
い。Regarding the distribution of the substituted alkyl groups by the number of carbon atoms, the one having 5 to 7 side chain alkyl groups has a peak (the ratio is 35% by weight to 50% by weight), and shows a substantially normal distribution shape. Those having a substituted alkyl group having 1 to 2 carbon atoms occupy approximately 5% by weight to 15% by weight in the aromatic hydrocarbon having a substituted alkyl group. Also, those having 12 or more carbon atoms are rarely present in ordinary diesel oil.
【0011】本発明の燃料油においては、側鎖アルキル
基における好ましい炭素数は3個〜11個であり、3個
未満であると潤滑性に効果がなく、また、11個を越え
ると熱的に不安定となる。In the fuel oil of the present invention, the preferred number of carbon atoms in the side chain alkyl group is 3 to 11, with less than 3 no effect on lubricity, and more than 11 results in thermal effects. Becomes unstable.
【0012】多環芳香族炭化水素としては、炭素数が3
個〜11個のアルキル基を側鎖置換基として有するもの
を80重量%以上、好ましくは90重量%以上含有する
ものである。これにより、硫黄分が0.05重量%以下
であっても潤滑性に優れる軽油となしうる。The polycyclic aromatic hydrocarbon has 3 carbon atoms.
It contains 80% by weight or more, and preferably 90% by weight or more of those having 1 to 11 alkyl groups as side chain substituents. Thereby, even if the sulfur content is 0.05% by weight or less, a gas oil having excellent lubricity can be obtained.
【0013】その詳細な理由は不明であるが、単環の芳
香族炭化水素は、芳香環のファンデルワールス力が小さ
いため、分子間の高荷重下での相互作用が少なく、アル
キル基を置換基として有していても軽油における潤滑性
に殆ど寄与しないと推測される。一方、多環芳香族炭化
水素として、長鎖アルキル置換多環芳香族炭化水素を8
0重量%以上含有するものは、高荷重下で分子間に働く
相互作用が強く、からみによる粘性が高くなるものと考
えられ、潤滑性に優れるものとできるものと推測してい
る。また、側鎖置換基においては、その数よりも、その
長さに影響されるものと推察される。Although the detailed reason for this is unclear, since monocyclic aromatic hydrocarbons have a small van der Waals force of the aromatic ring, there is little interaction between the molecules under high load, and the alkyl group is substituted. It is presumed that even if it has a base, it hardly contributes to the lubricity of light oil. On the other hand, as the polycyclic aromatic hydrocarbon, a long-chain alkyl-substituted polycyclic aromatic hydrocarbon is
It is considered that those containing 0% by weight or more have strong intermolecular interaction under high load and have high viscosity due to entanglement, and it is presumed that the lubricity can be excellent. In addition, it is presumed that the length of the side chain substituent is more affected by the length than the number thereof.
【0014】軽油中の多環芳香族炭化水素の含有量及び
側鎖アルキル基の炭素数分布は、軽油5gを試料とし、
n−ヘキサンで飽和分を抽出した後、カラムクロマト分
離〔クロマト管:25mmf×900mm、クロマトゲ
ル:シリカゲル(富士シリアル化学製#12)200g
(40g/g試料)、溶媒:トルエン600ml(3m
l/gゲル)〕することにより得た芳香族成分を質量分
析(イオン化法:FI)に付すことにより得られる。The content of polycyclic aromatic hydrocarbons in the gas oil and the carbon number distribution of the side chain alkyl group were measured using 5 g of gas oil as a sample,
After extracting the saturated component with n-hexane, column chromatographic separation [chromatography tube: 25 mmf × 900 mm, chromatogel: silica gel (Fuji Serial Chemical # 12) 200 g
(40 g / g sample), solvent: 600 ml of toluene (3 m
1 / g gel)] to obtain the aromatic component by mass spectrometry (ionization method: FI).
【0015】水添脱硫操作により、得られる軽油組成と
しては、例えば (1) 硫黄分 ・・・0.2重量% 多環芳香族炭化水素の含有量 ・・3.5重量% 2環芳香族炭化水素分 ・・2.9重量% 多環芳香族炭化水素中における長鎖アルキル置換多環芳香族炭化水素の占める 割合 ・・ 60重量% のもの、 (2) 硫黄分 ・・・0.01重量% 多環芳香族炭化水素化水素の含有量 ・・1.7重量% 2環芳香族炭化水素分 ・・1.5重量% 多環芳香族炭化水素中における長鎖アルキル置換多環芳香族炭化水素の占める 割合 ・・75重量% のものである。The gas oil composition obtained by the hydrodesulfurization operation is, for example, (1) sulfur content: 0.2% by weight, content of polycyclic aromatic hydrocarbons: 3.5% by weight: 2-ring aromatic Hydrocarbon content: 2.9 wt% Long-chain alkyl-substituted polycyclic aromatic hydrocarbons in polycyclic aromatic hydrocarbons: Proportion of 60 wt%, (2) Sulfur content: 0.01 Weight% Polycyclic aromatic hydrocarbon content ・ ・ 1.7% by weight Bicyclic aromatic hydrocarbon content ・ ・ 1.5% by weight Long-chain alkyl-substituted polycyclic aromatic hydrocarbon in polycyclic aromatic hydrocarbon The proportion of hydrocarbons: 75% by weight.
【0016】本発明の燃料油を製造するには、例えば、
水添処理した軽油に、芳香族炭化水素含有量の多い性状
の軽油を適宜混合して調製される。なお、芳香族成分量
のリッチなものとして、例えば原油の直留成分である重
油を接触分解して得られる接触分解軽油等を使用しても
よい。To produce the fuel oil of the present invention, for example,
It is prepared by appropriately mixing hydrogenated light oil with light oil having a high aromatic hydrocarbon content. As the rich aromatic component, for example, catalytically cracked gas oil obtained by catalytically cracking heavy oil which is a straight-run component of crude oil may be used.
【0017】また、本発明の燃料油には、必要に応じて
流動点降下剤、セタン価向上剤等を添加してもよい。If desired, a pour point depressant, a cetane number improver, etc. may be added to the fuel oil of the present invention.
【0018】[0018]
【作用及び発明の効果】本発明の燃料油は、耐摩耗剤等
の添加剤を添加することなく、軽油成分を調整するだけ
で耐摩耗性を付与しえるものであり、保存安定性に優れ
ると共に廉価な燃料油となしえるものである。INDUSTRIAL APPLICABILITY The fuel oil of the present invention is capable of imparting abrasion resistance only by adjusting the gas oil component without adding additives such as antiwear agents, and is excellent in storage stability. At the same time, it can be made into inexpensive fuel oil.
【0019】[0019]
【実施例】実施例で採用する耐摩耗試験について説明し
ておく。EXAMPLES The abrasion resistance test adopted in the examples will be described.
【0020】本発明で採用する耐摩耗試験は、ISO/
TC 22/SC7 N595で規定されるものであ
り、High frequency Reciprocating Rig装置(HFR
R、PCS社製)を使用し、下記のテスト条件で実施
し、摩耗痕径(μm)を測定するものである。本測定方
法では耐摩耗性に優れた軽油は摩耗痕径が小さく、逆に
耐摩耗性の劣る軽油は摩耗痕径が大きくなる。The wear resistance test adopted in the present invention is ISO /
High frequency reciprocating rig device (HFR) specified by TC 22 / SC7 N595.
R, manufactured by PCS Co., Ltd.) and used to measure the wear scar diameter (μm) under the following test conditions. According to this measuring method, light oil having excellent wear resistance has a small wear scar diameter, and conversely, light oil having poor wear resistance has a large wear scar diameter.
【0021】 液量 1±0.20ml ストローク長 1±0.02mm 周波数 50±1Hz 液温 25±2℃、又は60±2℃ 荷重 200g 試験時間 75±0.1分 液表面積 6±1cm2 (実施例1)原油の常圧蒸留により得られ、硫黄分が
0.05重量%までに脱硫処理された軽油留分に、芳香
族性の高い軽油基材を混合し、下記の表1に記載の性状
及び組成を有する軽油留分を得、本発明の燃料油である
試料油1とした。Liquid volume 1 ± 0.20 ml Stroke length 1 ± 0.02 mm Frequency 50 ± 1 Hz Liquid temperature 25 ± 2 ° C. or 60 ± 2 ° C. Load 200 g Test time 75 ± 0.1 min Liquid surface area 6 ± 1 cm 2 ( Example 1) A gas oil fraction having high aromaticity was mixed with a gas oil fraction obtained by atmospheric distillation of crude oil and desulfurized to a sulfur content of up to 0.05% by weight, and described in Table 1 below. A gas oil fraction having the above properties and composition was obtained and used as the sample oil 1 which is the fuel oil of the present invention.
【0022】(実施例2)原油の常圧蒸留により得ら
れ、硫黄分が0.05重量%までに脱硫処理された軽油
留分に実施例1と同様に操作して芳香族成分を調整し、
下記の表1に記載の性状及び組成を有する軽油留分を
得、本発明の燃料油である試料油2とした。Example 2 A light oil fraction obtained by atmospheric distillation of crude oil and desulfurized to a sulfur content of up to 0.05% by weight was processed in the same manner as in Example 1 to adjust aromatic components. ,
A gas oil fraction having the properties and composition shown in Table 1 below was obtained and used as a sample oil 2 as the fuel oil of the present invention.
【0023】(実施例3)原油の常圧蒸留により得ら
れ、硫黄分が0.01重量%までに脱硫処理された、下
記の表1の比較油1に、イソプロピルナフタレンを0.
8重量%、ジターシャリーブチルナフタレンを1.0重
量%の含有量となるように添加し、下記の性状及び組成
を有する軽油留分を得、本発明の燃料油である試料油3
を得た。Example 3 A comparative oil 1 of Table 1 below, which was obtained by atmospheric distillation of crude oil and desulfurized to a sulfur content of 0.01% by weight, was supplemented with isopropylnaphthalene of 0.1%.
8 wt% and ditert-butylnaphthalene were added so as to have a content of 1.0 wt% to obtain a gas oil fraction having the following properties and composition. Sample oil 3 as the fuel oil of the present invention
I got
【0024】(比較例1)下記の表1に記載の軽油を、
比較油1とした。(Comparative Example 1) The light oils listed in Table 1 below were
Comparative oil 1 was used.
【0025】(比較例2)原油の常圧蒸留により得ら
れ、硫黄分が0.2重量%までに脱硫処理された軽油留
分であって、下記の表1に記載の性状及び組成を有する
軽油留分を比較油2とした。(Comparative Example 2) A gas oil fraction obtained by atmospheric distillation of crude oil and desulfurized to a sulfur content of up to 0.2% by weight and having the properties and compositions shown in Table 1 below. The light oil fraction was designated as Comparative Oil 2.
【0026】上記で調製した試料油1〜3、比較油1〜
2について、60℃で耐摩耗試験を実施した。その結果
を同時に下記の表1に示す。Sample oils 1-3 prepared above and comparative oils 1-
For No. 2, an abrasion resistance test was performed at 60 ° C. The results are also shown in Table 1 below.
【0027】[0027]
【表1】 [Table 1]
【0028】表からわかるように、本発明の燃料油は、
耐摩耗性に優れることがわかる。As can be seen from the table, the fuel oil of the present invention is
It can be seen that it has excellent wear resistance.
Claims (1)
5重量%以下で、かつ2環以上の芳香族炭化水素の含有
量が3.5重量%〜15重量%であり、該2環以上の芳
香族炭化水素中に於ける、炭素数が3個〜11個の側鎖
アルキル基を有する、2環以上の芳香族炭化水素の占め
る割合を80重量%以上としたことを特徴とする燃料
油。1. A light oil fraction having a sulfur content of 0.0
5% by weight or less and the content of aromatic hydrocarbons having 2 or more rings is 3.5% by weight to 15% by weight, and the number of carbon atoms in the aromatic hydrocarbons having 2 or more rings is 3 A fuel oil characterized in that the proportion of aromatic hydrocarbons having two or more rings and having 11 to 11 side chain alkyl groups is 80% by weight or more.
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19443895A JPH0940975A (en) | 1995-07-31 | 1995-07-31 | Fuel oil |
| CA002182108A CA2182108A1 (en) | 1995-07-31 | 1996-07-25 | Gas oil |
| US08/690,445 US5730762A (en) | 1995-07-31 | 1996-07-26 | Gas oil (law451) |
| DE69619605T DE69619605T2 (en) | 1995-07-31 | 1996-07-30 | Gas oil composition |
| EP96305570A EP0757092B1 (en) | 1995-07-31 | 1996-07-30 | Gas oil |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19443895A JPH0940975A (en) | 1995-07-31 | 1995-07-31 | Fuel oil |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0940975A true JPH0940975A (en) | 1997-02-10 |
Family
ID=16324603
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19443895A Pending JPH0940975A (en) | 1995-07-31 | 1995-07-31 | Fuel oil |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0940975A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013175878A1 (en) | 2012-05-24 | 2013-11-28 | Nok株式会社 | Polyamine-vulcanizable highly saturated nitrile rubber composition |
| WO2013175877A1 (en) | 2012-05-24 | 2013-11-28 | Nok株式会社 | Polyamine-vulcanizable highly saturated nitrile rubber composition |
-
1995
- 1995-07-31 JP JP19443895A patent/JPH0940975A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013175878A1 (en) | 2012-05-24 | 2013-11-28 | Nok株式会社 | Polyamine-vulcanizable highly saturated nitrile rubber composition |
| WO2013175877A1 (en) | 2012-05-24 | 2013-11-28 | Nok株式会社 | Polyamine-vulcanizable highly saturated nitrile rubber composition |
| US9403972B2 (en) | 2012-05-24 | 2016-08-02 | Nok Corporation | Polaymine curable, highly saturated nitrile rubber composition |
| US9404003B2 (en) | 2012-05-24 | 2016-08-02 | Nok Corporation | Polyamine curable, highly saturated nitrile rubber composition |
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