JPH0826331B2 - Kerosene - Google Patents
KeroseneInfo
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- JPH0826331B2 JPH0826331B2 JP1322200A JP32220089A JPH0826331B2 JP H0826331 B2 JPH0826331 B2 JP H0826331B2 JP 1322200 A JP1322200 A JP 1322200A JP 32220089 A JP32220089 A JP 32220089A JP H0826331 B2 JPH0826331 B2 JP H0826331B2
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- Prior art keywords
- kerosene
- oil
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- odor
- present
- Prior art date
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- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は灯油に関し、詳しくは暖房用燃料として優れ
た備えた灯油に関する。TECHNICAL FIELD The present invention relates to kerosene, and more particularly to kerosene excellent as a fuel for heating.
[従来の技術とその課題] 灯油は家庭用の暖房用燃料として広く使われている
が、石油ストーブへ給油する場合などに発生する石油臭
や手への付着による不快感などが使用者に嫌われる欠点
があった。また、開放式の石油ストーブにあっては、点
火時及び消化時に未燃焼ないしは不完全燃焼の炭化水素
化合物や含酸素化合物が発生し、不快な臭気を放つ欠点
もあった。そして、使用者が要望する石油ストーブに対
する安全性や快適性(NOX,炭化水素化合物,CO,SO2など
の発生量が少なく、かつ不快臭を伴わない)なども年々
レベルを高めている。そのため、石油ストーブに使用さ
れる灯油は、使用者の要望を十分に応え得るものではな
ければならない。[Prior art and its problems] Kerosene is widely used as a heating fuel for home use. However, users do not like the smell of petroleum or the discomfort caused by sticking to their hands when refueling an oil stove. There was a shortcoming. Further, in the open type oil stove, there is a drawback that unburned or incompletely burned hydrocarbon compounds and oxygen-containing compounds are generated at the time of ignition and digestion, and an unpleasant odor is emitted. Further, the safety and comfort of petroleum stoves demanded by users (the amount of NO X , hydrocarbon compounds, CO, SO 2, etc. generated is small and there is no unpleasant odor) and the like are increasing year by year. Therefore, the kerosene used in the oil stove must be able to sufficiently meet the needs of users.
灯油一般に認められる上記のような欠点を解決する方
法としては、灯油気化触媒を用いる方法(特公昭59−16
814号公報)、灯油に消臭剤を添加する方法(特公昭54
−32003号公報)、n−パラフィンおよびイソパラフィ
ン類よりなる灯油(特開昭63−150380号公報)などが提
案されている。As a method for solving the above-mentioned drawbacks generally recognized in kerosene, a method using a kerosene vaporization catalyst (Japanese Patent Publication No. 59-16
No. 814), a method of adding a deodorant to kerosene (JP-B-54)
-32003), kerosene composed of n-paraffins and isoparaffins (JP-A-63-150380), and the like.
しかしながら、灯油気化触媒を用いる方法では、触媒
が経時的に劣化するため、長期間クリーンな燃焼を持続
させることが困難であった。灯油に消臭剤を添加する方
法は、その調合が面倒であるばかりでなく、匂いに対す
る個人の好みの問題があるため、あまり効果的ではなか
った。またn−パラフィンおよびイソパラフィン類より
なる灯油は、製造コストが大幅に上昇し、価格の高い灯
油になるという問題があった。However, in the method using the kerosene vaporization catalyst, it is difficult to maintain clean combustion for a long time because the catalyst deteriorates with time. The method of adding a deodorant to kerosene was not very effective because of its troublesome preparation and the problem of individual preference for odor. In addition, kerosene composed of n-paraffins and isoparaffins has a problem that the production cost is significantly increased and the kerosene becomes expensive.
一方、本発明者らは上記の要求を満足する灯油を先に
開発し、既に特許出願をしている(特願昭63−264929
号)。On the other hand, the present inventors have previously developed kerosene that satisfies the above requirements and have already applied for a patent (Japanese Patent Application No. 63-264929).
issue).
本発明者らはさらに性能の優れた灯油を開発すべく研
究を重ねた結果、留出温度、硫黄分、芳香族分、ナフタ
レン分が燃焼性、排気ガスの清浄性および取り扱い時の
臭気と深い関係を有することを見出し、本発明の完成す
るに至った。As a result of repeated studies to develop kerosene with further excellent performance, the present inventors have found that the distillation temperature, sulfur content, aromatic content, and naphthalene content are combustible, exhaust gas cleanliness, and deep odor during handling. The inventors have found that they have a relationship, and have completed the present invention.
本発明の目的は燃焼性に優れ、排気ガスの清浄性も高
く、しかも取り扱い時の臭気が少ないという特性を備え
た高性能な灯油を提供することにある。An object of the present invention is to provide a high-performance kerosene having excellent combustibility, high exhaust gas cleanliness, and low odor during handling.
[課題を解決するための手段] 本発明の灯油は、 (1)次式で規定される灯油燃焼性劣化指数(KCDI)が
1.0以下、 KCDI=1.95WNA+0.06V(>T220℃) (2)硫黄分含有量が灯油全量に対し1wtppm以下、かつ (3)次式で規定される灯油臭気指数(KSI)が1.5以下 KSI=0.01V(≦T180℃)+1.2iogVA であることを特徴とする。[Means for Solving the Problems] The kerosene of the present invention has (1) a kerosene flammability deterioration index (KCDI) defined by the following equation:
1.0 or less, KCDI = 1.95W NA + 0.06V (> T 220 ℃ ) (2) Sulfur content is 1wtppm or less based on the total amount of kerosene, and (3) Kerosene odor index (KSI) defined by the following formula is 1.5 The following is characterized by KSI = 0.01V (≦ T 180 ° C. ) + 1.2iogV A.
上式中、WNAは灯油全量に対するナフタレン分の量(t
w%)を、V(>T220℃)は灯油全量に対する沸点220
℃を越える留分の量(vol%)を、V(≦T180℃)は灯
油全量に対する沸点180℃以下の留分の量(vol%)を、
VAは灯油全量に対する芳香族分の量(vol%)をそれぞ
れ示す。In the above formula, W NA is the amount of naphthalene (t
w%), V (> T 220 ° C ) is the boiling point of 220 relative to the total amount of kerosene.
The amount of the fraction (vol%) exceeding ℃, V (≦ T 180 ℃ ) is the amount of the fraction having a boiling point of 180 ℃ or less (vol%) to the total amount of kerosene,
V A represents the amount of aromatic components (vol%) relative to the total amount of kerosene.
以下、本発明の内容をより詳細に説明する。 Hereinafter, the content of the present invention will be described in more detail.
本発明の灯油は、(1)KCDI≦1.0、(2)硫黄分含
有量が灯油全量に対し1wtppm以下、(3)KSI≦1.5の3
つの条件を全て満たすことが必要である。上記条件のう
ち1つも満たさない場合には性能が劣るため好ましくな
い。The kerosene of the present invention has (1) KCDI ≦ 1.0, (2) sulfur content of 1 wtppm or less relative to the total amount of kerosene, and (3) KSI ≦ 1.5.
It is necessary to meet all one condition. If none of the above conditions are satisfied, the performance is inferior, which is not preferable.
すなわち、(1)の条件は、灯油全量に対するナフタ
レン分の量(wt%)を1.95倍と、灯油全量に対する沸点
220℃を越える留分の量(vol%)の0.06倍との和で算出
されるKCDIの値が1.0以下、好ましくは0.8以下であるこ
とを示している。ここで、ナフタレン分には、ナフタレ
ン、アセナフテンおよびこれらのアルキル化物、例えば
メチルナフタレン、エチルナフタレン、メチルアセナフ
タレン、エチルアセナフタレンなどが含まれる。KCDIの
値が1.0を越える場合には、灯油の燃焼性が悪くなるの
で好ましくない。なお、WNAおよびV(>T220℃)の個
々の値は特に限定されないが、WNAは0.1wt%以下、好ま
しくは0.08wt%以下であり、V(>T220℃)は10vol%
以下、好ましくは9.0vol%以下であることが望ましい。That is, condition (1) is that the amount of naphthalene (wt%) is 1.95 times the total amount of kerosene, and the boiling point is
It shows that the value of KCDI calculated from the sum of the amount of the fraction (vol%) exceeding 220 ° C. and 0.06 times is 1.0 or less, preferably 0.8 or less. Here, the naphthalene component includes naphthalene, acenaphthene, and alkylated products thereof, such as methylnaphthalene, ethylnaphthalene, methylacenaphthalene, and ethylacenaphthalene. If the KCDI value exceeds 1.0, the combustibility of kerosene deteriorates, which is not preferable. The individual values of W NA and V (> T 220 ° C ) are not particularly limited, but W NA is 0.1 wt% or less, preferably 0.08 wt% or less, and V (> T 220 ° C ) is 10 vol%.
Below, it is desirable to be below 9.0vol% preferably.
また、本発明の灯油は、(2)の条件に示される通
り、硫黄分含有量が灯油全量に対し1wtppm以下、好まし
くは0.8wtppm以下であることが必要である。硫黄分含有
量が1wtppmを越える場合には、燃焼中における排ガス中
のSO2量が多くなる。また、燃焼排ガスによる燃焼機器
等の腐食が大きくなる。Further, the kerosene of the present invention is required to have a sulfur content of 1 wtppm or less, preferably 0.8 wtppm or less based on the total amount of kerosene, as shown in the condition (2). If the sulfur content exceeds 1 wtppm, the amount of SO 2 in the exhaust gas during combustion will increase. In addition, the corrosion of combustion equipment and the like due to the combustion exhaust gas increases.
さらに、(3)の条件は、灯油全量に対する沸点180
℃以下の留分の量(vol%)の0.01倍と、灯油全量に対
する芳香族分の量(vol%)の対数の1.2倍との和で算出
されるKSIの値が1.5以下、好ましくは1.4以下であるこ
とを示している。ここで対数とは常用対数を意味する。
KSIの値が1.6を越える場合は、取り扱い時の臭気が大き
くなるので好ましくない。なお、V(≦T180℃)およ
びVAの個々の値は、特に限定されるものではない。例え
ば、V(≦T180℃)が大きい場合でもKSI≦1.5を満足
させる値以下にVAが小さければ臭気に問題はなく、同様
にVAが大きくてもV(≦T180℃)がKSI≦1.5を満たす
値以下であれば、取り扱い時の臭気は十分少ない。Furthermore, the condition (3) is that the boiling point is 180 relative to the total amount of kerosene.
The KSI value calculated by adding 0.01 times the amount of the fraction (vol%) below ℃ and 1.2 times the logarithm of the amount of the aromatic content (vol%) to the total amount of kerosene is 1.5 or less, preferably 1.4. It indicates the following. Here, logarithm means common logarithm.
When the KSI value exceeds 1.6, the odor during handling increases, which is not preferable. The individual values of V (≦ T 180 ° C. ) and V A are not particularly limited. For example, even if V (≦ T 180 ° C. ) is large, there is no odor problem if V A is smaller than a value satisfying KSI ≦ 1.5. Similarly, even if V A is large, V (≦ T 180 ° C. ) If the value is less than or equal to ≦ 1.5, the odor during handling is sufficiently low.
念のため付言すれば、本発明でいう留出温度は、JIS
K 2254の燃料油蒸留試験方法で規定されている留出温度
を、ナフタレン分はJIS K 2276のナフタレン分試験方法
(紫外分光光度法)による値を、芳香族分含有量はJIS
K 2536の燃料油炭化水素成分試験方法(けい光指示薬吸
着法)により測定される値を、硫黄分含有量はJIS K 25
41に規定される微量電量滴定式酸化法により測定される
値をそれぞれ示している。In addition, as a reminder, the distillation temperature in the present invention is JIS
The distillation temperature specified by the fuel oil distillation test method of K 2254, the naphthalene content is the value according to the JIS K 2276 naphthalene content test method (ultraviolet spectrophotometric method), and the aromatic content is JIS
The value measured by the K 2536 fuel oil hydrocarbon component test method (fluorescent indicator adsorption method) is based on JIS K 25
The values measured by the microcoulometric titration oxidation method specified in 41 are shown.
本発明の灯油は、上記(1)〜(3)の条件を満たし
ていることにより、燃焼性および排ガスの清浄性に優
れ、取り扱い時の臭気が少ない灯油であるが、さらに、
JIS K 2203に規定される1号灯油の条件を満たしている
ことが好ましい。すなわち、反応が中性、引火点が40℃
以上、95%留出温度が270℃以下、煙点が23以上、銅板
腐食(50℃,3h)が1以下、色(セーボルト)が+25以
上であることが好ましい。The kerosene of the present invention is a kerosene that is excellent in combustibility and cleanliness of exhaust gas and has little odor during handling because it satisfies the above conditions (1) to (3).
It is preferable that the conditions for No. 1 kerosene specified in JIS K 2203 are satisfied. That is, the reaction is neutral and the flash point is 40 ° C.
As described above, it is preferable that the 95% distillation temperature is 270 ° C. or less, the smoke point is 23 or more, the copper plate corrosion (50 ° C., 3 hours) is 1 or less, and the color (Seybolt) is +25 or more.
本発明の灯油の製造方法は任意であって、原油を蒸留
して得ることもできる。このほか、芳香族炭化水素含有
量の少ない灯油留分、例えばインドネシアのミナス原油
等を蒸留して180℃から220℃の留分を多く含む粗灯油を
得て、それを水素化精製することによって得ることもで
きる。また、芳香族炭化水素含有量が10 vol%以上の灯
油留分については、芳香族炭化水素を水素添加してナフ
テン炭化水素等に改質することによって、本発明の灯油
を得ることができる。さらに、重質軽油を水添分解装置
にかけて得られる灯油留分、いわゆる水添分解灯油を用
いることもできる。The method for producing kerosene of the present invention is arbitrary and can be obtained by distilling crude oil. In addition, a kerosene fraction with a low aromatic hydrocarbon content, such as Minas crude oil from Indonesia, is distilled to obtain crude kerosene containing a large fraction from 180 ° C to 220 ° C and hydrorefining it. You can also get it. Further, with respect to the kerosene fraction having an aromatic hydrocarbon content of 10 vol% or more, the kerosene of the present invention can be obtained by hydrogenating the aromatic hydrocarbon to reform it into a naphthene hydrocarbon or the like. Further, it is also possible to use a kerosene fraction obtained by subjecting heavy gas oil to a hydrocracking device, so-called hydrogenolysis kerosene.
本発明の灯油には、必要に応じてフェノール系、アミ
ン系などの酸化防止剤、シッフ型化合物やチオアミド型
化合物などの金属不活性化剤、有機りん系化合物などの
表面着火防止剤、こはく酸イミド、ポリアルキルアミ
ン、ポリエーテルアミンなどの清浄分散剤、多価アルコ
ールおよびそのエーテルなどの氷結防止剤、有機酸のア
ルカリ金属塩やアルカリ土類金属塩、高級アルコールの
硫酸エステルなどの助燃剤、アニオン系界面活性剤、カ
チオン系界面活性剤、両性界面活性剤などの帯電防止剤
およびアゾ染料などの着色剤を包含する公知の燃料油添
加剤を1種または数種組み合わせて添加してもよい。こ
れら燃料添加剤の添加量は任意であるが、通常、その合
計添加量は0.005〜0.5重量%、好ましくは0.01〜0.05重
量%の範囲にある。The kerosene of the present invention includes, if necessary, an antioxidant such as a phenol type or amine type, a metal deactivator such as a Schiff type compound or a thioamide type compound, a surface ignition inhibitor such as an organic phosphorus type compound, and succinic acid. Detergents and dispersants such as imides, polyalkyl amines and polyether amines, anti-icing agents such as polyhydric alcohols and their ethers, alkali metal salts and alkaline earth metal salts of organic acids, combustion improvers such as sulfuric acid esters of higher alcohols, Known fuel oil additives including antistatic agents such as anionic surfactants, cationic surfactants and amphoteric surfactants and colorants such as azo dyes may be added alone or in combination of two or more. . The amount of these fuel additives added is arbitrary, but the total amount added is usually in the range of 0.005 to 0.5% by weight, preferably 0.01 to 0.05% by weight.
本発明の灯油はいわゆる民生用暖房機器、例えば各種
ストーブ類あるいは石油式給油器などのに好ましく用い
られるが、なかでも芯上下式石油ストーブ、石油ファン
ヒーターなどの開放式石油ストーブの燃料として最も好
ましく用いられる。さらに、直火式の食品乾燥用燃料、
工業用燃料、石油発動機用燃料、ソルベントなど各種用
途に好ましく使用できる。The kerosene of the present invention is preferably used for so-called consumer heating equipment, for example, various stoves or petroleum type oil feeders, and among them, most preferable as a fuel for open-ended petroleum stoves such as core up-down oil stoves and oil fan heaters. Used. In addition, direct fire type food drying fuel,
It can be preferably used for various purposes such as industrial fuel, petroleum engine fuel, and solvent.
[実施例] 以下、本発明の内容を実施例および比較例によりさら
に具体的に説明する。[Examples] Hereinafter, the content of the present invention will be described more specifically with reference to Examples and Comparative Examples.
実施例1 トッパーより得られたスマトラ系原油の灯油留分をニ
ッケル−モリブデン系触媒が充填されている灯油用水素
化精製装置で処理した。処理条件は320℃、40kg/cm3、L
HSV=4であった。得られた精製油(A)を精密蒸留
し、166.5〜230℃の沸点範囲を持つ高品質灯油を得た。
この性状を表−1に示す。この油のWNAは0.05、V(>
T220℃)は6.0であり、KCDIは0.45であった。またV
(≦T180℃)は30.0、VAは8.8であり、KSIは1.43とな
った。また硫黄分は1ppm以下であった。Example 1 A kerosene fraction of Sumatra crude oil obtained from a topper was treated with a kerosene hydrorefining apparatus filled with a nickel-molybdenum catalyst. Processing conditions are 320 ℃, 40kg / cm 3 , L
HSV = 4. The refined oil (A) thus obtained was subjected to precision distillation to obtain high quality kerosene having a boiling point range of 166.5 to 230 ° C.
The properties are shown in Table 1. The W NA of this oil is 0.05, V (>
T 220 ) was 6.0 and KCDI was 0.45. Also V
(≦ T 180 ° C. ) was 30.0, V A was 8.8, and KSI was 1.43. The sulfur content was 1 ppm or less.
実施例2 実施例1で得られた精製油(A)を精密蒸留し、沸点
範囲164.5〜230.5℃の留分を得た。その性状を表−1に
示す。この油のWNAは0.06、V(>T220℃)は8.5であ
り、KCDIは0.61となる。またV(≦T180℃)は30.0、V
Aは8.7であり、KSIは1.42となる。また硫黄分は1ppm以
下であった。Example 2 The refined oil (A) obtained in Example 1 was precision distilled to obtain a fraction having a boiling point range of 164.5 to 230.5 ° C. The properties are shown in Table 1. This oil has a W NA of 0.06, a V (> T 220 ° C ) of 8.5, and a KCDI of 0.61. Also, V (≦ T 180 ℃ ) is 30.0, V
A is 8.7 and KSI is 1.42. The sulfur content was 1 ppm or less.
実施例3 アラビア系の市販のJIS 1号灯油を白金触媒を用いて
全芳香族分が10%以下になるように核水素化し、さらに
精密蒸留を用い、沸点範囲165.5〜232.5℃の高品質灯油
を得た。得られた油の性状を表−1に示す。この油のW
NAは0.1、V(>T220℃)は6.5であり、KCDIは0.59と
なる。さらにV(≦T180℃)は27.5、VAは8.0であり、
KSIは1.36となる。この油の硫黄分は1ppm以下であっ
た。Example 3 A commercially available Arabian-based JIS No. 1 kerosene was nuclear hydrogenated with a platinum catalyst so that the total aromatic content was 10% or less, and further precision distillation was used to produce high-quality kerosene with a boiling point range of 165.5 to 232.5 ° C. Got The properties of the obtained oil are shown in Table 1. W of this oil
NA is 0.1, V (> T 220 ° C ) is 6.5, and KCDI is 0.59. Furthermore, V (≦ T 180 ℃ ) is 27.5, V A is 8.0,
The KSI will be 1.36. The sulfur content of this oil was less than 1 ppm.
比較例1〜3 実施例1で示したスマトラ系の精製油(A)を精留せ
ずに用いたもの(比較例1)、精製油(A)を精留して
重質分を除去した油(比較例2)および精製油(A)の
軽質分を除去した油(比較例3)を製造した。各試料油
の性状を表−1に示す。これらの試料油のKCDIは各々1.
28,0.45および1.74となり、KSIは各々1.52,1.57および
1.19となる。Comparative Examples 1 to 3 The Sumatra refined oil (A) shown in Example 1 was used without rectification (Comparative Example 1), and the refined oil (A) was rectified to remove heavy components. An oil (Comparative Example 2) and an oil (Comparative Example 3) from which the light component of the refined oil (A) was removed were produced. The properties of each sample oil are shown in Table-1. The KCDI of these sample oils is 1.
28,0.45 and 1.74 with KSI of 1.52,1.57 and
It becomes 1.19.
比較例4,5 アラビア系の市販のJIS 1号灯油(比較例4)と、そ
れを精留蒸留して軽質分と重質分を除去した試料油(比
較例5)を製造した。各試料油の性状を表−1に示す。
これらの試料油のKCDIは各々2.66および2.32となり、KS
Iは各々1.73と1.62となる。Comparative Examples 4 and 5 A commercially available Arabic-type JIS No. 1 kerosene (Comparative Example 4) and a sample oil (Comparative Example 5) from which light and heavy components were removed by rectifying and distilling it were produced. The properties of each sample oil are shown in Table-1.
The KCDIs of these sample oils are 2.66 and 2.32, respectively.
I are 1.73 and 1.62 respectively.
実施例1〜3および比較例1〜5の灯油を用い、以下
に示す試験を行った。 The following tests were conducted using the kerosene of Examples 1 to 3 and Comparative Examples 1 to 5.
1.臭気官能試験(取り扱い時) 取り扱い時の臭気を想定して20名の被験者による臭気
官能試験を各試料油について実施した。試験は各々の試
料を100ccの共栓付きのガラス容器に80cc入れ、栓を10
秒間開放し、後半の5秒間で試料の臭気を嗅ぎ、臭気の
強度を表−2に示す6段階臭気強度判定尺度を用いて測
定した。結果を表−3に示す。1. Odor sensory test (at the time of handling) An odor sensory test was performed on each sample oil by 20 subjects assuming the odor at the time of handling. In the test, 80 cc of each sample was put in a glass container with a 100 cc stopper, and the stopper was 10
The sample was opened for 2 seconds, and the odor of the sample was sniffed in the latter 5 seconds, and the odor intensity was measured using the 6-stage odor intensity evaluation scale shown in Table 2. The results are shown in Table-3.
2.ストーブ燃焼試験 実施例1〜3および比較例1〜5の試料油を用い、芯
上下式ストーブ(松下電器(株)製)により、芯の目盛
を最も小さくした燃焼条件で、1000時間の連続燃焼を行
った。燃料の違いによる燃焼製の差異は、燃焼期間中の
燃料消費量の変化を燃焼開始時を100として示した。さ
らに1000時間燃焼後の芯の汚れ具合を市販のJIS 1号灯
油を5とした5段階の芯の黒化度(1が最も汚れが少な
い)として測定した。結果を第1図に示す。 2. Stove Combustion Test Using the sample oils of Examples 1 to 3 and Comparative Examples 1 to 5, a core top and bottom stove (manufactured by Matsushita Electric Industrial Co., Ltd.) was used for combustion for 1000 hours under the combustion condition with the smallest scale of the core. Continuous combustion was performed. The difference in fuel consumption due to the difference in fuel is shown by the change in fuel consumption during the combustion period, with 100 at the start of combustion. Further, the degree of soiling of the wick after burning for 1000 hours was measured as a degree of blackening of the wick in five steps (1 being the least dirty) with a commercially available JIS No. 1 kerosene as 5. The results are shown in Fig. 1.
臭気官能試験およびストーブ燃焼試験の試験結果から
明らかなように、本発明の灯油は比較例の灯油に比べて
取り扱い時の臭気が少なく、また、燃料消費量の低下も
著しく小さく、芯の黒化度もいずれも1であり、燃焼性
が良好なことが実証された。さらに本発明の灯油は燃焼
性が良好なため、点火および消化時の臭気も比較例の試
料油に比べて少なく、さらに定常燃焼時の未燃の炭化水
素類や一酸化炭素も少ないことも確認した。比較例2の
灯油は燃料消費量の低下および芯の黒化度は本発明と同
等であるが、取り扱い時の臭気が大きく、また、比較例
3の灯油は取り扱い時の臭気は本発明と同等であるが、
燃料消費量および芯の黒化度に関して大幅に劣ってい
る。As is clear from the test results of the odor sensory test and the stove combustion test, the kerosene of the present invention has less odor during handling than the kerosene of the comparative example, and the decrease in fuel consumption is also significantly small, resulting in blackening of the core. The degree was 1 in each case, which proved that the flammability was good. Further, since the kerosene of the present invention has good flammability, it was confirmed that the odor at the time of ignition and digestion was smaller than that of the sample oil of the comparative example, and the unburned hydrocarbons and carbon monoxide at the time of steady combustion were also small. did. The kerosene of Comparative Example 2 has the same fuel consumption reduction and the degree of blackening of the wick as those of the present invention, but has a large odor during handling, and the kerosene of Comparative Example 3 has the same odor of during handling as the present invention. In Although,
Significantly inferior in terms of fuel consumption and blackening of the wick.
[発明の効果] 本発明の高品質灯油は従来の市販のJIS 1号に比べて
取り扱い時の臭気がほとんどなく、さらに燃焼性が良好
なことにより最も油の性状に敏感な芯上下式のストーブ
に用いた場合でも、燃料消費量の低下が著しく少なく、
また芯の汚れもほとんどない。さらに燃焼排ガスも清浄
であり、家庭生活をより健康で過ごすという国民の願い
にも合致すると考えられる。[Effects of the Invention] The high-quality kerosene of the present invention has almost no odor during handling as compared with the conventional commercially available JIS No. 1, and because it has good flammability, it is the top and bottom stove that is most sensitive to the properties of oil. Even when used for, the decrease in fuel consumption is extremely small,
Also, there is almost no stain on the core. Furthermore, the combustion exhaust gas is also clean, which is considered to be in line with the people's desire to live a healthier family life.
第1図はストーブ燃焼試験の結果(芯上下式ストーブの
燃料消費量の変化および芯の黒化度)を示すグラフであ
る。FIG. 1 is a graph showing the results of the stove combustion test (changes in fuel consumption of the upper and lower wick stoves and degree of blackening of the wick).
Claims (2)
表される灯油燃焼性劣化指数(KCDI)が1.0以下、 (2)硫黄分含有量が灯油全量に対し1wtppm以下、かつ (3)式0.01V(≦T180℃)+1.2 logVAで表される灯
油臭気指数(KSI)が1.5以下 であることを特徴とする灯油。 1. A kerosene flammability deterioration index (KCDI) represented by the formula (1) 1.95 W NA +0.06 V (> T 220 ° C. ) is 1.0 or less, and (2) sulfur content is 1 wtppm with respect to the total amount of kerosene. or less and (3) 0.01V (≦ T 180 ℃) +1.2 kerosene logV kerosene odor index represented by a (KSI) is equal to or more than 1.5.
1記載の灯油。2. The kerosene according to claim 1, which is obtained by distilling crude oil.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1322200A JPH0826331B2 (en) | 1989-12-12 | 1989-12-12 | Kerosene |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1322200A JPH0826331B2 (en) | 1989-12-12 | 1989-12-12 | Kerosene |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03182594A JPH03182594A (en) | 1991-08-08 |
JPH0826331B2 true JPH0826331B2 (en) | 1996-03-13 |
Family
ID=18141070
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1322200A Expired - Lifetime JPH0826331B2 (en) | 1989-12-12 | 1989-12-12 | Kerosene |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0826331B2 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001279269A (en) * | 2000-03-31 | 2001-10-10 | Idemitsu Kosan Co Ltd | Method for producing fuel oil for fuel cell and hydrogen for fuel cell |
JP2001279275A (en) * | 2000-03-31 | 2001-10-10 | Idemitsu Kosan Co Ltd | Method for producing fuel oil for fuel cell and hydrogen for fuel cell |
JP2001294874A (en) * | 2000-04-13 | 2001-10-23 | Idemitsu Kosan Co Ltd | Fuel oil for kerosene fuel cells |
JP4565834B2 (en) | 2003-12-19 | 2010-10-20 | 昭和シェル石油株式会社 | Kerosene composition |
JP4903994B2 (en) * | 2004-11-26 | 2012-03-28 | 昭和シェル石油株式会社 | Kerosene composition |
JP5348821B2 (en) * | 2005-05-26 | 2013-11-20 | Jx日鉱日石エネルギー株式会社 | Kerosene composition |
JP4739841B2 (en) * | 2005-07-25 | 2011-08-03 | コスモ石油株式会社 | Kerosene composition |
JP4881663B2 (en) * | 2006-06-20 | 2012-02-22 | コスモ石油株式会社 | Kerosene composition and method for producing kerosene composition |
JP4890137B2 (en) * | 2006-07-21 | 2012-03-07 | コスモ石油株式会社 | Kerosene composition |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2556311B2 (en) * | 1986-07-04 | 1996-11-20 | 日本石油化学株式会社 | Process for producing hydrocarbon mixture solvent |
JPS63150380A (en) * | 1986-12-13 | 1988-06-23 | Idemitsu Kosan Co Ltd | improved kerosene |
-
1989
- 1989-12-12 JP JP1322200A patent/JPH0826331B2/en not_active Expired - Lifetime
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JPH03182594A (en) | 1991-08-08 |
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