JP3949501B2 - Fuel oil composition - Google Patents

Fuel oil composition Download PDF

Info

Publication number
JP3949501B2
JP3949501B2 JP2002119107A JP2002119107A JP3949501B2 JP 3949501 B2 JP3949501 B2 JP 3949501B2 JP 2002119107 A JP2002119107 A JP 2002119107A JP 2002119107 A JP2002119107 A JP 2002119107A JP 3949501 B2 JP3949501 B2 JP 3949501B2
Authority
JP
Japan
Prior art keywords
less
base material
fuel oil
oil composition
oil
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 - Fee Related
Application number
JP2002119107A
Other languages
Japanese (ja)
Other versions
JP2003313566A (en
Inventor
幹治 諸岡
繁洋 岩田
一仁 上島
貞憲 澤田
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.)
Idemitsu Kosan Co Ltd
Original Assignee
Idemitsu Kosan 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 Idemitsu Kosan Co Ltd filed Critical Idemitsu Kosan Co Ltd
Priority to JP2002119107A priority Critical patent/JP3949501B2/en
Publication of JP2003313566A publication Critical patent/JP2003313566A/en
Application granted granted Critical
Publication of JP3949501B2 publication Critical patent/JP3949501B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Description

【0001】
【発明の属する技術分野】
本発明は、燃料油組成物に関し、詳しくは発熱量が高く、低温での流動性に優れ、燃焼性が良好で、かつ環境負荷の低い燃料油組成物に関する。
【0002】
【従来の技術】
通常、内燃用及び外燃用燃料油としては、灯油、A重油、C重油等があり、それぞれ用途に応じて使い分けられている。灯油は、硫黄含有量、窒素含有量及び残留炭素分の含有量が極めて低いため、環境負荷が低く、通常家庭用の暖房機器に好適に使用される。しかしながら、発熱量が低いため、さらに発熱量を必要とする用途に使用するには不十分である。
また、A重油は安定供給の面で優れており、灯油に比較して高い発熱量を持つことから、小型ボイラー、ディーゼルエンジン等の用途に好適に使用されるが、最近はさらに高い発熱量を持つ燃料油組成物が要求されている。
【0003】
A重油の発熱量を向上させる方法としては種々の方法が提案されている。例えば高沸点留分の基材の混合比率を大きくしたり、接触分解軽質軽油(以下、LCO(light cyclic oil)という場合がある)の混合比率を大きくしたりする方法である。
しかしながら、前者の方法では直留系基材の高沸点留分にはパラフィン分が多いため、最終製品の低温流動性が低下する場合があり、後者の方法では使用時に着火不良が起きたり、煤が発生する等の燃焼不良が起こる場合がある。
【0004】
一方、直接脱硫装置から留出する直接脱硫軽油は、低環境負荷であり、良好な燃焼性を有するが、通常発熱量が十分ではなく、発熱量を高くなるように調製した場合には低温流動性に劣るものとなる。
また、A重油より高い発熱量を有する燃料油としてC重油があるが、高粘度のため、加温設備が必要になり、取り扱いが不便なことに加え、硫黄分、窒素分、残留炭素分が高い等、環境への影響が大きいという欠点がある。
【0005】
【発明が解決しようとする課題】
本発明は、上述のような状況下、環境負荷が低く、安定性、低温流動性及び燃焼性が良好で、かつ従来より高い発熱量を有する燃料油組成物を提供することを目的とするものである。
【0006】
【課題を解決するための手段】
本発明者らは、上記目的を達成すべく種々の研究を重ねた結果、直接脱硫装置から留出する直接脱硫軽油基材35〜75容量%及び接触分解軽質軽油基材10〜45容量%を含有し、セタン指数40以上、密度0.8763以上、硫黄含有量0.10質量%以下、曇り点(CP)3℃以下、目詰まり点(CFPP)−10℃以下、流動点(PP)−10℃以下、かつ50℃での粘度が3.50mm2/s以下である燃料油組成物であって、前記直接脱硫軽油基材がセタン指数40以上、密度0.885以上、硫黄含有量0.03質量%以下、かつ50℃での粘度が5.00mm2/s以下であり、前記接触分解軽質軽油基材がセタン指数25以上、密度0.920以上、硫黄含有量0.350質量%以下であることを特徴とする燃料油組成物が上記目的を達成することを見出し、本発明を完成したものである。
【0007】
【発明の実施の形態】
本発明の燃料油組成物は、セタン指数40以上、密度0.8763以上、硫黄含有量0.10質量%以下、曇り点3℃以下、目詰まり点−10℃以下、流動点−10℃以下、かつ50℃での粘度が3.50mm2/s以下のものである。これらの物性を有することによって、以下のような利点がある。
セタン指数が40以上であると、燃焼性が確保される。燃焼性の観点から、セタン指数は45以上が好ましく、さらには50以上が好ましい。
密度が0.8763未満であると、十分な発熱量が得られない。高カロリーを確保するとの観点から、密度が0.8800以上であることがさらに好ましい。硫黄含有量が0.10質量%以下であると、燃焼した場合の硫黄酸化物量を低減することができ、環境負荷を低減することができる。また酸露点上昇による煙突などの低温腐蝕が起きにくいといった利点がある。
曇り点3℃以下、目詰まり点−10℃以下、流動点−10℃以下であることによって低温での流動性が確保できる。低温流動性の観点から曇り点は0℃以下、目詰まり点は−15℃以下、流動点は−15℃以下がさらに好ましい。
また、50℃での粘度が3.50mm2/s以下であることで燃焼性を高く維持でき、取り扱い性を容易にすることができる。
【0008】
また、本発明の燃料油は、直接脱硫軽油基材及び接触分解軽質軽油基材を含有する。
直接脱硫軽油基材とは、原油を常圧蒸留装置によって分留した残渣油を直接脱硫装置で脱硫した際に得られる軽油留分をいう。直接脱硫装置とは、常圧蒸留残渣油を触媒の存在下、高温・高圧下で水素化脱硫する装置をいう。ここで使用する触媒としては、通常使用される水素化脱硫触媒であれば特に限定されず、Co−Mo系触媒、Ni−Mo系触媒、Ni−W系触媒、Ni−Co−Mo系触媒等が挙げられる。反応条件としては、反応温度350〜450℃、反応圧力20〜200kg/cm2、水素/油比200〜2000Nl/l、液空間速度(LHSV)0.5〜5hr-1の範囲が好ましい。
【0009】
本発明の燃料油組成物において、前記直接脱硫軽油基材は、セタン指数40以上、密度0.885以上、硫黄含有量0.03質量%以下、かつ50℃での粘度5.00mm2/s以下のものである。
セタン指数が40以上であることで最終製品の燃焼性が確保され、密度が0.885以上であることで製品の高カロリー性を確保することができ、硫黄含有量が0.03質量%以下であることで製品の低硫黄化が確保できる。また、50℃での粘度が5.00mm2/s以下であることが、製品の性状を確保するために必要であり、性状確保の観点から4.50mm2/s以下であることが好ましく、さらには3.30〜4.50mm2/sの範囲であることが好ましい。
上記燃料油組成物の性状を確保するためには、該直接脱硫軽油基材の含有量は燃料油組成物に対して35〜75容量%の範囲であることが必要である。
【0010】
また、上述の性状を有する直接脱硫軽油基材を効率よく製造する方法として、常圧残渣油に接触分解軽質軽油を混合して直接脱硫装置に通油する方法が好ましい。接触分解軽質軽油の混合量としては、直接脱硫装置の処理能力等により適宜選択し得るが、効率的に製造するとの観点から5〜20容量%の範囲であることが好ましい。
【0011】
次に、接触分解軽質軽油基材とは、一般には重質留分等を流動接触分解(以下「(R)FCC」という)装置で分解した軽油留分のうち軽質の部分をいう。
ここで、(R)FCC装置とは、常圧重質軽油、減圧軽油、常圧残油などの重質留分を流動する触媒と高温で接触させ、重質留分を分解して、ガソリン留分や軽油留分を得る装置をいう。ここで使用する触媒としては、通常(R)FCC触媒として使用されるものであれば限定されないが、特にSiO2−Al23やゼオライト等の固体酸触媒が好適である。反応条件としては、反応温度450〜550℃、反応圧力0.1〜0.5MPa、接触時間0.1〜2秒、触媒/油比5〜20kg/kgの範囲が好ましい。また、(R)FCC装置では、流動する触媒が反応塔から連続的に抜き出され、再生塔にて空気燃焼により再生される。
【0012】
本発明において、前記接触分解軽質軽油基材はセタン指数25以上、密度0.920以上、硫黄含有量0.350質量%以下のものである。
セタン指数が25以上であることで最終製品の燃焼性が確保され、密度が0.920以上であることで製品の高カロリー性を確保することができ、また硫黄含有量が0.350質量%以下であることで、製品の低硫黄化が確保できる。
前記燃料油組成物の性状を確保するために、該接触分解軽質軽油基材の含有量は燃料油組成物に対して10〜45容量%の範囲であることが必要であり、特に製品のセタン指数、密度を好ましい範囲とするためには、さらに12〜30容量%の範囲とすることが好ましい。
尚、本発明の燃料油組成物には必要に応じ、本発明の効果を損なわない範囲で、水添脱硫軽油(DGO)、水素化分解軽油(HCGO)、脱ろう軽油(DWGO)等の基材を配合することができる。
【0013】
また、本発明の燃料油組成物には、灯油基材を混合することができ、灯油基材の混合によって、製品の低温流動性を確保することが容易になる。製品の低温流動性及び発熱量等の製品性状を確保するとの観点から、その添加量は0〜20容量%の範囲が好ましく、特には10〜18容量%の範囲が好ましい。
さらに、本発明にかかる燃料油には、製品の低温流動性を確保するために、残留炭素源を0.1〜0.5容量%添加することが好ましい。
【0014】
また、製品の低温流動性を確保するために流動性向上剤を添加することが好ましい。流動性向上剤の添加量としては、十分な低温流動性が得られるとともに他の物性にも悪影響を及ぼさないとの観点から、100〜500質量ppmの範囲であることが好ましい。
流動性向上剤としては、燃料油組成物の低温流動性を向上させるものであれば特に限定されないが、エチレン・ビニル共重合物又はトリスアミンのモノ脂肪酸エステル/エチレン・プロピレン共重合物を主成分とするものが好ましい。
尚、本発明にかかる燃料油は、本発明の目的を害さない範囲内で、上記基材以外に燃料油に用いられる種々の基材を用いることができる。具体的には、脱硫した直留軽油(DGO)、水素化分解軽油(HCGO)、脱ワックスした直留軽油(DWGO)等、またはこれらの留分を適宜混合して用いることができる。
また、本発明の燃料油組成物には、所望に応じて各種添加剤を添加することができ、例えば、本発明の燃料油組成物を内燃用燃料とする場合には、必要に応じ、セタン価向上剤を添加することができる。
【0015】
【実施例】
次に、本発明を実施例によりさらに詳細に説明するが、本発明は、これらの例によってなんら限定されるものではない。
各種測定方法
1)密度
JIS K 2249に準じて測定した。
2)引火点
JIS K 2265に準じて測定した。
3)動粘度
JIS K 2283に準じて測定した。
4)硫黄含有量
JIS K 2541に準じて測定した。
5)10%残炭
JIS K 2270に準じて測定した。
6)曇り点
JIS K 2269に準じて測定した。
7)目詰まり点
JIS K 2288に準じて測定した。
8)流動点
JIS K 2269に準じて測定した。
9)セタン指数
JIS K 2204−1992に準じて測定した。
10)ASTM色
JIS K 2580に準じて測定した。
【0016】
評価方法
1)低温流動性
曇り点が3℃以下、目詰まり点が−10℃以下、かつ、流動点が−10℃である場合には○、これらの要件の少なくとも1つを満足しない場合には×と評価した。
2)燃焼性
セタン指数が40以上、かつ550℃での動粘度が3.50mm2/s以下である場合に○、これらの要件の少なくとも一方を満足しない場合には×と評価した。
3)カロリー
カロリーが0.8800以上である場合に◎、0.8763以上0.8800未満である場合に〇、0.8763未満である場合には×と評価した。
【0017】
実施例1,2、比較例1〜4
第1表に示す基材を、第2表に示す配合量で配合して、燃料油組成物を製造した。それぞれの燃料油組成物について、密度、ASTM色、引火点、動粘度(@50℃)、硫黄分、10%残留炭素、曇り点、目詰まり点、50%留出温度、90%留出温度及びセタン指数を測定し、また低温流動性及び燃焼性の評価を実施した。その結果を第3表に示す。
【0018】
【表1】

Figure 0003949501
*1 DSGO−1;常圧蒸留残渣油(RC)に接触分解軽質軽油(LCO)を10容量%混合し、脱硫処理して得た直接脱硫軽油基材
*2 DSGO−2;常圧蒸留残渣油(RC)を脱硫処理して得た直接脱硫軽油基材
*3 LCO;接触分解軽質軽油基材
*4 DGO;直留軽油を脱硫処理した脱硫軽油基材
*5 K−1;脱硫灯油基材
*6 RC;常圧蒸留残渣油
【0019】
【表2】
Figure 0003949501
*7 FI;流動性向上剤(インフィニアムジャパン社製「INFINEUM R240」)
【0020】
【表3】
Figure 0003949501
【0021】
【発明の効果】
本発明にかかる燃料油組成物は環境負荷が低く、安定性、低温流動性及び燃焼性が良好で、かつ高い発熱量を有する。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a fuel oil composition, and more particularly to a fuel oil composition having a high calorific value, excellent fluidity at low temperatures, good combustibility, and low environmental burden.
[0002]
[Prior art]
In general, fuel oils for internal combustion and external combustion include kerosene, heavy oil A, heavy fuel oil C, and the like, which are properly used depending on the application. Kerosene has a very low sulfur content, nitrogen content, and residual carbon content, and therefore has a low environmental impact, and is usually suitably used for domestic heating equipment. However, since the calorific value is low, it is insufficient for use in applications that require a further calorific value.
In addition, heavy oil A is superior in terms of stable supply and has a higher calorific value than kerosene, so it is preferably used for applications such as small boilers and diesel engines. A fuel oil composition is required.
[0003]
Various methods have been proposed as methods for improving the calorific value of A heavy oil. For example, it is a method of increasing the mixing ratio of the base material of the high-boiling fraction or increasing the mixing ratio of catalytically cracked light gas oil (hereinafter sometimes referred to as LCO (light cyclic oil)).
However, in the former method, the high boiling fraction of the straight-run base material contains a large amount of paraffin, so the low-temperature fluidity of the final product may be reduced. In the latter method, poor ignition may occur during use. In some cases, a combustion failure such as the occurrence of spillage occurs.
[0004]
On the other hand, the direct desulfurized light oil distilled from the direct desulfurization apparatus has a low environmental load and good combustibility, but usually has a low calorific value, and when it is prepared to have a high calorific value, it flows at low temperature. It becomes inferior.
In addition, fuel oil C has a higher calorific value than fuel oil A, but because of its high viscosity, heating equipment is required and handling is inconvenient, as well as sulfur, nitrogen, and residual carbon. There is a drawback that the impact on the environment is large, such as high.
[0005]
[Problems to be solved by the invention]
An object of the present invention is to provide a fuel oil composition having a low environmental load, good stability, low-temperature fluidity and combustibility, and a higher calorific value than the conventional one under the above-mentioned circumstances. It is.
[0006]
[Means for Solving the Problems]
As a result of repeating various studies to achieve the above object, the present inventors have obtained 35 to 75% by volume of a direct desulfurized gas oil base material distilled from a direct desulfurization apparatus and 10 to 45% by volume of a catalytically cracked light gas oil base material. Cetane index 40 or more, density 0.8763 or more, sulfur content 0.10 mass% or less, cloud point (CP) 3 ° C. or less, clogging point (CFPP) −10 ° C. or less, pour point (PP) − A fuel oil composition having a viscosity at 10 ° C. or lower and a viscosity at 50 ° C. of 3.50 mm 2 / s or lower, wherein the direct desulfurized gas oil base material has a cetane index of 40 or higher, a density of 0.885 or higher, and a sulfur content of 0 0.03 mass% or less and a viscosity at 50 ° C. of 5.00 mm 2 / s or less, the catalytically cracked light gas oil base material has a cetane index of 25 or more, a density of 0.920 or more, and a sulfur content of 0.350 mass%. A fuel oil composition characterized by the following: It found that to achieve the above object, and completed the present invention.
[0007]
DETAILED DESCRIPTION OF THE INVENTION
The fuel oil composition of the present invention has a cetane index of 40 or more, a density of 0.8763 or more, a sulfur content of 0.10% by mass or less, a cloud point of 3 ° C. or less, a clogging point of −10 ° C. or less, and a pour point of −10 ° C. or less. And a viscosity at 50 ° C. of 3.50 mm 2 / s or less. By having these physical properties, there are the following advantages.
When the cetane index is 40 or more, combustibility is ensured. From the viewpoint of flammability, the cetane index is preferably 45 or more, and more preferably 50 or more.
If the density is less than 0.8763, a sufficient calorific value cannot be obtained. From the viewpoint of securing high calories, the density is more preferably 0.8800 or more. When the sulfur content is 0.10% by mass or less, the amount of sulfur oxides when combusted can be reduced, and the environmental load can be reduced. In addition, there is an advantage that low temperature corrosion such as a chimney due to an increase in acid dew point does not easily occur.
By having a cloud point of 3 ° C. or lower, a clogging point of −10 ° C. or lower, and a pour point of −10 ° C. or lower, fluidity at a low temperature can be secured. From the viewpoint of low temperature fluidity, the cloud point is more preferably 0 ° C. or less, the clogging point is −15 ° C. or less, and the pour point is more preferably −15 ° C. or less.
Further, when the viscosity at 50 ° C. is 3.50 mm 2 / s or less, the combustibility can be maintained high, and the handleability can be facilitated.
[0008]
The fuel oil of the present invention contains a direct desulfurized light oil base and a catalytically cracked light light oil base.
The direct desulfurized light oil base material refers to a light oil fraction obtained when a residual oil obtained by fractionating crude oil by an atmospheric distillation apparatus is desulfurized by a direct desulfurization apparatus. The direct desulfurization apparatus is an apparatus for hydrodesulfurizing atmospheric distillation residue oil in the presence of a catalyst at high temperature and high pressure. The catalyst used here is not particularly limited as long as it is a commonly used hydrodesulfurization catalyst. Co-Mo catalyst, Ni-Mo catalyst, Ni-W catalyst, Ni-Co-Mo catalyst, etc. Is mentioned. As reaction conditions, a reaction temperature of 350 to 450 ° C., a reaction pressure of 20 to 200 kg / cm 2 , a hydrogen / oil ratio of 200 to 2000 Nl / l, and a liquid space velocity (LHSV) of 0.5 to 5 hr −1 are preferable.
[0009]
In the fuel oil composition of the present invention, the direct desulfurized gas oil base material has a cetane index of 40 or more, a density of 0.885 or more, a sulfur content of 0.03% by mass or less, and a viscosity at 50 ° C. of 5.00 mm 2 / s. It is as follows.
When the cetane index is 40 or more, the combustibility of the final product is ensured, and when the density is 0.885 or more, the high caloric property of the product can be ensured, and the sulfur content is 0.03% by mass or less. Therefore, it is possible to secure low sulfur of the product. Further, the viscosity at 50 ° C. is 5.00 mm 2 / s or less, which is necessary for securing the properties of the product, and from the viewpoint of securing properties, it is preferably 4.50 mm 2 / s or less, Furthermore, it is preferable that it is the range of 3.30-4.50mm < 2 > / s.
In order to ensure the properties of the fuel oil composition, it is necessary that the content of the direct desulfurized gas oil base is in the range of 35 to 75% by volume with respect to the fuel oil composition.
[0010]
In addition, as a method for efficiently producing a direct desulfurized light oil base material having the above-described properties, a method in which a catalytically cracked light gas oil is mixed with an atmospheric residue and directly passed through a desulfurization apparatus is preferable. The mixing amount of the catalytically cracked light gas oil can be appropriately selected depending on the processing capacity of the direct desulfurization apparatus, but is preferably in the range of 5 to 20% by volume from the viewpoint of efficient production.
[0011]
Next, the catalytically cracked light gas oil base generally refers to a light portion of a light oil fraction obtained by cracking a heavy fraction or the like with a fluid catalytic cracking (hereinafter referred to as “(R) FCC”) apparatus.
Here, the (R) FCC device is a gasoline that brings heavy fractions such as atmospheric heavy gas oil, vacuum gas oil and atmospheric residue into contact with a flowing catalyst at a high temperature, decomposes the heavy fraction, and produces gasoline. An apparatus for obtaining a fraction or a light oil fraction. The catalyst used here is not limited as long as it is usually used as an (R) FCC catalyst, but a solid acid catalyst such as SiO 2 —Al 2 O 3 or zeolite is particularly suitable. The reaction conditions are preferably a reaction temperature of 450 to 550 ° C., a reaction pressure of 0.1 to 0.5 MPa, a contact time of 0.1 to 2 seconds, and a catalyst / oil ratio of 5 to 20 kg / kg. In the (R) FCC apparatus, the flowing catalyst is continuously extracted from the reaction tower and regenerated by air combustion in the regeneration tower.
[0012]
In the present invention, the catalytically cracked light gas oil base material has a cetane index of 25 or more, a density of 0.920 or more, and a sulfur content of 0.350% by mass or less.
When the cetane index is 25 or more, the flammability of the final product is secured, and when the density is 0.920 or more, the high calorie property of the product can be secured, and the sulfur content is 0.350 mass%. By making it below, it is possible to secure low sulfur of the product.
In order to ensure the properties of the fuel oil composition, the content of the catalytically cracked light gas oil base is required to be in the range of 10 to 45% by volume with respect to the fuel oil composition. In order to make the index and density within the preferable ranges, it is further preferable to set them within the range of 12 to 30% by volume.
It should be noted that the fuel oil composition of the present invention includes a base such as hydrodesulfurized light oil (DGO), hydrocracked light oil (HCGO), dewaxed light oil (DWGO), etc. as long as the effects of the present invention are not impaired. Materials can be blended.
[0013]
Moreover, a kerosene base material can be mixed with the fuel oil composition of this invention, and it becomes easy to ensure the low temperature fluidity | liquidity of a product by mixing of a kerosene base material. From the viewpoint of ensuring product properties such as low-temperature fluidity and calorific value of the product, the addition amount is preferably in the range of 0 to 20% by volume, and particularly preferably in the range of 10 to 18% by volume.
Furthermore, it is preferable to add 0.1 to 0.5% by volume of a residual carbon source to the fuel oil according to the present invention in order to ensure low temperature fluidity of the product.
[0014]
Moreover, it is preferable to add a fluidity improver in order to ensure the low temperature fluidity of the product. The addition amount of the fluidity improver is preferably in the range of 100 to 500 ppm by mass from the viewpoint that sufficient low-temperature fluidity can be obtained and other physical properties are not adversely affected.
The fluidity improver is not particularly limited as long as it improves the low temperature fluidity of the fuel oil composition, but the main component is an ethylene / vinyl copolymer or a trisamine mono-fatty acid ester / ethylene / propylene copolymer. Those that do are preferred.
In addition, the fuel oil concerning this invention can use the various base material used for fuel oil other than the said base material in the range which does not impair the objective of this invention. Specifically, desulfurized straight-run gas oil (DGO), hydrocracked light oil (HCGO), dewaxed straight-run gas oil (DWGO), or a mixture of these fractions can be used as appropriate.
In addition, various additives can be added to the fuel oil composition of the present invention as desired. For example, when the fuel oil composition of the present invention is used as a fuel for internal combustion, cetane is used as necessary. A value improver can be added.
[0015]
【Example】
EXAMPLES Next, although an Example demonstrates this invention further in detail, this invention is not limited at all by these examples.
Various measuring methods 1) Density Measured according to JIS K 2249.
2) Flash point Measured according to JIS K 2265.
3) Kinematic viscosity Measured according to JIS K 2283.
4) Sulfur content Measured according to JIS K2541.
5) 10% residual charcoal Measured according to JIS K 2270.
6) Cloud point Measured according to JIS K 2269.
7) Clogging point Measured according to JIS K 2288.
8) Pour point Measured according to JIS K 2269.
9) Cetane index Measured according to JIS K 2204-1992.
10) Measured according to ASTM color JIS K 2580.
[0016]
Evaluation method 1) When the low temperature fluidity cloud point is 3 ° C. or less, the clogging point is −10 ° C. or less, and the pour point is −10 ° C., ○, when at least one of these requirements is not satisfied Was evaluated as x.
2) When the combustible cetane index was 40 or more and the kinematic viscosity at 550 ° C. was 3.50 mm 2 / s or less, it was evaluated as ◯, and when at least one of these requirements was not satisfied, it was evaluated as x.
3) When the calorie calorie was 0.8800 or more, it was evaluated as ◎, when it was 0.8763 or more and less than 0.8800, ◯, and when it was less than 0.8763, it was evaluated as ×.
[0017]
Examples 1 and 2 and Comparative Examples 1 to 4
The fuel oil composition was manufactured by blending the base materials shown in Table 1 in the blending amounts shown in Table 2. For each fuel oil composition, density, ASTM color, flash point, kinematic viscosity (@ 50 ° C), sulfur content, 10% residual carbon, cloud point, clogging point, 50% distillation temperature, 90% distillation temperature The cetane index was measured, and low-temperature fluidity and flammability were evaluated. The results are shown in Table 3.
[0018]
[Table 1]
Figure 0003949501
* 1 DSGO-1: Direct desulfurized gas oil base material obtained by mixing 10% by volume of catalytic cracked light gas oil (LCO) with atmospheric distillation residue oil (RC) * 2 DSGO-2; atmospheric distillation residue Direct desulfurized light oil base * 3 LCO obtained by desulfurizing oil (RC) * 4 DGO; Desulfurized light oil base obtained by desulfurizing straight run diesel oil * 5 K-1; Desulfurized kerosene base Material * 6 RC; atmospheric distillation residue oil
[Table 2]
Figure 0003949501
* 7 FI: Fluidity improver ("INFINEUM R240" manufactured by Infinium Japan)
[0020]
[Table 3]
Figure 0003949501
[0021]
【The invention's effect】
The fuel oil composition according to the present invention has a low environmental load, good stability, low temperature fluidity and combustibility, and a high calorific value.

Claims (4)

直接脱硫装置から留出する直接脱硫軽油基材35〜75容量%及び接触分解軽質軽油基材10〜45容量%を含有し、セタン指数40以上、密度0.8763以上、硫黄含有量0.10質量%以下、曇り点3℃以下、目詰まり点−10℃以下、流動点−10℃以下、かつ50℃での粘度が3.50mm2/s以下である燃料油組成物であって、前記直接脱硫軽油基材がセタン指数40以上、密度0.885以上、硫黄含有量0.03質量%以下、かつ50℃での粘度が5.00mm2/s以下であり、前記接触分解軽質軽油基材がセタン指数25以上、密度0.920以上、硫黄含有量0.350質量%以下であることを特徴とする燃料油組成物。It contains 35 to 75% by volume of a direct desulfurized gas oil base material and 10 to 45% by volume of a catalytic cracked light gas oil base material distilled from a direct desulfurization unit, has a cetane index of 40 or more, a density of 0.8763 or more, and a sulfur content of 0.10. A fuel oil composition having a mass% or less, a cloud point of 3 ° C. or less, a clogging point of −10 ° C. or less, a pour point of −10 ° C. or less, and a viscosity at 50 ° C. of 3.50 mm 2 / s or less, The direct desulfurized light oil base material has a cetane index of 40 or more, a density of 0.885 or more, a sulfur content of 0.03% by mass or less, and a viscosity at 50 ° C. of 5.00 mm 2 / s or less. A fuel oil composition, wherein the material has a cetane index of 25 or more, a density of 0.920 or more, and a sulfur content of 0.350% by mass or less. 前記直接脱硫軽油基材が、接触分解軽質軽油基材を常圧蒸留残渣油に混合し、該混合油を直接脱硫装置にて脱硫して得られる脱硫軽油基材であることを特徴とする請求項1記載の燃料油組成物。The direct desulfurized light oil base material is a desulfurized light oil base material obtained by mixing a catalytic cracked light light oil base material with an atmospheric distillation residue oil and desulfurizing the mixed oil directly in a desulfurization apparatus. Item 4. The fuel oil composition according to Item 1. さらに灯油基材0〜20容量%及び/又は残留炭素源0.1〜0.5容量%を配合することを特徴とする請求項1又は2に記載の燃料油組成物。Furthermore, 0-20 volume% of kerosene base materials and / or 0.1-0.5 volume% of residual carbon sources are mix | blended, The fuel oil composition of Claim 1 or 2 characterized by the above-mentioned. さらに流動性向上剤100〜500質量ppm配合することを特徴とする請求項1又は2に記載の燃料油組成物。Furthermore, 100-500 mass ppm of fluidity improvers is mix | blended, The fuel oil composition of Claim 1 or 2 characterized by the above-mentioned.
JP2002119107A 2002-04-22 2002-04-22 Fuel oil composition Expired - Fee Related JP3949501B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2002119107A JP3949501B2 (en) 2002-04-22 2002-04-22 Fuel oil composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2002119107A JP3949501B2 (en) 2002-04-22 2002-04-22 Fuel oil composition

Publications (2)

Publication Number Publication Date
JP2003313566A JP2003313566A (en) 2003-11-06
JP3949501B2 true JP3949501B2 (en) 2007-07-25

Family

ID=29535762

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002119107A Expired - Fee Related JP3949501B2 (en) 2002-04-22 2002-04-22 Fuel oil composition

Country Status (1)

Country Link
JP (1) JP3949501B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5507043B2 (en) * 2007-09-27 2014-05-28 出光興産株式会社 Fuel oil composition
JP5153289B2 (en) * 2007-10-16 2013-02-27 昭和シェル石油株式会社 A heavy oil composition

Also Published As

Publication number Publication date
JP2003313566A (en) 2003-11-06

Similar Documents

Publication Publication Date Title
JP2018165365A (en) Fuel oil composition and method for producing the same
JP4409677B2 (en) Fuel oil composition
JP5507043B2 (en) Fuel oil composition
JP4827349B2 (en) Fuel oil composition
JP2003105349A (en) Method for producing kerosene
JPWO2020138272A1 (en) Fuel oil composition
JP3999912B2 (en) A heavy oil composition
JP4577925B2 (en) A heavy oil composition
JP2000144152A (en) High-performance a-heavy oil
JP4039760B2 (en) Kerosene and method for producing the same
JPH1121568A (en) Diesel fuel oil composition
JP5105858B2 (en) Hydrocarbon fuel oil and method for producing the same
JP2008248175A (en) Gas oil base material and gas oil composition
JP3999911B2 (en) A heavy oil composition
JP4885628B2 (en) Method for producing A heavy oil composition
JP3949501B2 (en) Fuel oil composition
JP4885627B2 (en) Method for producing A heavy oil composition
JP3981487B2 (en) A heavy oil composition with high total calorific value and ultra-low sulfur
JP2003096474A (en) Fuel oil composition
EP3781654B1 (en) Diesel fuel with improved ignition characteristics
JP4052773B2 (en) Light oil composition
JP3817182B2 (en) Fuel oil composition
JP2002180070A (en) Fuel oil for boiler/industrial furnace
JP5105895B2 (en) Light oil composition
JP2007269926A (en) A-heavy oil composition

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20041112

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20070320

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20070327

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20070418

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

Ref document number: 3949501

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100427

Year of fee payment: 3

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130427

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20140427

Year of fee payment: 7

LAPS Cancellation because of no payment of annual fees