JPH03182594A - Kerosine - Google Patents
KerosineInfo
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- JPH03182594A JPH03182594A JP32220089A JP32220089A JPH03182594A JP H03182594 A JPH03182594 A JP H03182594A JP 32220089 A JP32220089 A JP 32220089A JP 32220089 A JP32220089 A JP 32220089A JP H03182594 A JPH03182594 A JP H03182594A
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Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
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
性能を備えた灯油に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to kerosene, and more particularly to kerosene that has excellent performance as a heating fuel.
[従来の技術とその課題J
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具や手
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。[Conventional technology and its issues J Kerosene is widely used as a household heating fuel, but
Users dislike the discomfort caused by the oil getting on their hands and tools when refueling a kerosene stove. In addition, open-type kerosene stoves have the disadvantage that unburnt or incompletely burned hydrocarbon compounds and oxygen-containing compounds are generated during ignition and extinguishing, giving off an unpleasant odor.
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。Furthermore, the safety and comfort of kerosene stoves that users desire (NOX, hydrocarbon compounds, 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
ものでなければならない。(The amount of SO2 etc. generated is small and there is no unpleasant odor)
The level is also increasing year by year. Therefore, the kerosene used in kerosene stoves must be able to fully meet the needs of the 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59−1
6814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63−15038
0号公報)などが提案されている。As a method to solve the above-mentioned drawbacks generally recognized in kerosene, there is a method using a kerosene vaporization catalyst (Japanese Patent Publication No. 59-1
6814), a method of adding a deodorant to kerosene (Japanese Patent Publication No. 54-32003), kerosene consisting of n-paraffins and isoparaffins (Japanese Patent Publication No. 63-15038)
Publication No. 0), etc. have been proposed.
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てなく、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、砺格の高い灯油に
なるという問題があった。However, in the method using a kerosene vaporization catalyst, the catalyst deteriorates over time, making it difficult to maintain clean combustion for a long period of time. The method of adding deodorizing agents to kerosene has not been very effective, not only because its formulation is cumbersome, but also because of the issue of personal taste in odor. Further, kerosene made of n-paraffins and isoparaffins has a problem in that the production cost increases significantly and the kerosene has a high purity.
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83−2649
29号)。On the other hand, the present inventors have developed kerosene that satisfies the above requirements and have already filed a patent application (Japanese Patent Application No. 83-2649).
No. 29).
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、本発明を完成する
に至った。As a result of repeated research to develop kerosene with even better performance, the present inventors found that the distillation temperature, sulfur content, aromatic content, and naphthalene content significantly affected flammability, exhaust gas cleanliness, and odor during handling. We have found that there is a relationship between the two, 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 that has excellent combustibility, high exhaust gas cleanliness, and low odor when handled.
[課題をM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(KCD
I >が1.0以下
KCDI −1,95WNA+ 0.06V C> T
22ot)(2)硫黄分含有量が灯油全量に対し1
vtppm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,OIV (≦T +so℃) + 1.
21ogV p。[Means for determining the problem] The kerosene of the present invention has a kerosene flammability deterioration index (KCD) defined by the following formula: (1)
I> is 1.0 or less KCDI -1,95WNA+ 0.06V C>T
22 ot) (2) Sulfur content is 1 per total amount of kerosene
vtppm or less, and the kerosene odor index (KSI) defined by the (3> equation) is 1.
5 or less KSI -0, OIV (≦T +so℃) + 1.
21ogV p.
であることを特徴とする。It is characterized by
上式中、WNAは灯油全量に対するナフタレン分の量(
νt%)を、V(>722゜いは灯油全量に対する沸点
220℃を越える留分のjl(VOI%)を、V(≦T
180T)は灯油全量に対する沸点180℃以下の留分
のji(vo1%)を、vAは灯油全量に対する芳香族
分の量(vo1%)をそれぞれ示す。In the above formula, WNA is the amount of naphthalene in the total amount of kerosene (
νt%), V (>722° or jl (VOI%) of the fraction with a boiling point exceeding 220°C relative to the total amount of kerosene, V(≦T
180T) represents the ji (vo1%) of the fraction with a boiling point of 180° C. or lower relative to the total amount of kerosene, and vA represents the amount of aromatic components (vo1%) 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 explained in more detail.
本発明の灯油は、(1) XCDl51.0 、 (2
)硫黄分含有量が灯油全量に対し1 wtpp−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。The kerosene of the present invention has (1) XCDl51.0, (2
) Sulfur content is 1 wtpp- or less based on the total amount of kerosene,
(3) It is necessary to satisfy all three conditions of KSI*1.5.
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。If any one of the above conditions is not satisfied, the performance will be poor, 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j;1(vt%)の1.95倍と、灯油全量に対
する沸点220℃を越える留分の量(vo1%)のa、
(16倍との和で算出されるKCD 1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、メチルアセナフテン、エチルアセナ
フテンなどが含まれる。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。In other words, the conditions (1) are: j; 1.95 times the naphthalene content (vt%) relative to the total amount of kerosene;
(It shows that the value of KCD 1 calculated by the sum of , for example methylnaphthalene,
Includes ethylnaphthalene, methylacenaphthene, ethylacenaphthene, etc. If the value of KCDI exceeds 1.0, the flammability of kerosene deteriorates, which is not preferable.
なお、WNAおよびv (>T2□。りの個々の値は特
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 (> T z□o
、:)は10vo1%以下、好ましくは9.0vo1%
以下であることが望ましい。Note that the individual values of WNA and v (>T2□) are not particularly limited, but WNA is 0.1 wt% or less, preferably 0.08 wt% or less,
, :) is 10vo1% or less, preferably 9.0vo1%
The following is desirable.
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1 vtppm以下、好
ましくはo、5vtpp口以下であることが必要である
。硫黄分含有量が1νtppl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。In addition, the kerosene of the present invention has the following conditions as shown in condition (2):
It is necessary that the sulfur content be 1 vtppm or less, preferably 0.5 vtpp or less, based on the total amount of kerosene. When the sulfur content exceeds 1 νtppl, the amount of SO2 in the exhaust gas during combustion increases.
また、燃焼排ガスによる燃焼機器等の腐食が大きくなる
。In addition, corrosion of combustion equipment and the like due to 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(vo1%)の0,01倍と、灯油全
量に対する芳香族分のJl(vo1%)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、■(≦T18゜いおよびvAの個々の値は、特
に限定されるものではない。例えば、■(≦T+5oy
)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■いが
大きくてもV(≦T+go℃)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 for the total amount of kerosene.
0.01 times the amount of fraction below ℃ (vo1%) and 1.2 of the logarithm of the aromatic content Jl (vo1%) with respect to the total amount of kerosene.
This indicates that the value of KSI calculated by the sum of the multiplication factor is 1.5 or less, preferably 1.4 or less. Logarithm here means common logarithm. If the KSI value exceeds 1.6, it is not preferable because the odor during handling becomes large. Note that the individual values of ■(≦T18° and vA are not particularly limited. For example, ■(≦T+5oy
) is large but if VA is small enough to satisfy KSI≦1.5, there is no odor problem; similarly, even if ■ is large, V (≦T+go℃) is below a value that satisfies KSI≦1.5. If so, 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の燃料部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 227B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 253Bの燃料油炭化水素
成分試験方広(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 2541に規定され
る微ffi@jiIiIN定式酸化法により測定される
値をそれぞれ示している。Just to be sure, the distillation temperature in the present invention is based on JIS
The distillation temperature specified in the fuel part distillation test method of K 2254, the value of the naphthalene content according to the naphthalene content test method (ultraviolet spectrophotometry) of JIS K 227B, and the aromatic content determined by the fuel part of JIS K 253B. The value measured by oil hydrocarbon component testing method (fluorescent indicator adsorption method) is shown, and the sulfur content is the value measured by the ffi@jiIiIN formula oxidation method specified in JIS K 2541. .
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、JI
S 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℃。Since the kerosene of the present invention satisfies the conditions (1) to (3) above, it has excellent combustibility and exhaust gas cleanliness,
Kerosene has little odor when handled, but in addition, JI
It is preferable that the conditions for No. 1 kerosene specified in S K 2203 are met. That is, the reaction is neutral, the flash point is 40°C or higher, the 95% distillation temperature is 270°C or lower, the smoke point is 23 or higher, and copper plate corrosion (50°C).
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。3h) is preferably 1 or less, and the color (Saybold) is preferably +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 vo1
%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
解装置を用いることもできる。The method for producing kerosene of the present invention is arbitrary, and it can also be obtained by distilling crude oil. In addition, by distilling kerosene fractions with low aromatic hydrocarbon content, such as Indonesian Minas crude oil, to obtain crude kerosene containing a large fraction of 180°C to 220°C, and then hydrorefining it. You can also get it. In addition, the aromatic hydrocarbon content is 10 vol.
% or more of kerosene fraction, the kerosene of the present invention can be obtained by hydrogenating aromatic hydrocarbons and reforming them into naphthenic hydrocarbons and the like. Furthermore, it is also possible to use a kerosene fraction obtained by subjecting heavy gas oil to a hydrogen cracking apparatus, a so-called hydrogen cracking apparatus.
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、シップ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at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1i19tl、好ましく
は0.O1〜0.05重量%の範囲にある。The kerosene of the present invention may optionally contain antioxidants such as phenolics and amines, metal deactivators such as ship-type compounds and thioamide-type compounds, surface ignition inhibitors such as organophosphorus compounds, and succinic acid. imide, polyalkylamine,
Cleaning and dispersing agents such as polyether amines, anti-icing agents such as polyhydric alcohols and their ethers, alkali metal salts and alkaline earth metal salts of atom acids, combustion improvers such as sulfuric esters of higher alcohols, anionic surfactants , cationic surfactants, amphoteric surfactants, and other known fuel oil additives, including antistatic agents such as cationic surfactants, amphoteric surfactants, and colorants such as azo dyes, may be added singly or in combination. The amount of these fuel additives added is arbitrary, but usually the total amount added is 0.005 to 0.5 weight 1i19 tl, preferably 0.5 to 19 tl. O ranges from 1 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 in so-called consumer heating equipment, such as various types of stoves and kerosene oil dispensers, but is most preferably used as a fuel for open-type kerosene stoves such as top-and-bottom wick type kerosene stoves and kerosene fan heaters. used. Furthermore, it can be preferably used in various applications such as direct-fired food drying fuel, 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 contents of the present invention will be explained in more detail with reference to Examples and Comparative Examples.
実施例1
トラパーより得られたスマトラ系原油の灯油留分をニッ
ケルー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/
a’、L)ISV−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W
NAは0.05、V (> T 2zow)は6.0で
あり、KCDIは0.45テあった。またv(≦Te8
or)は30.0、vAは8.8であり、KSIは1.
43となった。また硫黄分はIpP−以下であった。Example 1 A kerosene fraction of Sumatran crude oil obtained from Trapar was treated in a kerosene hydrorefining unit filled with a nickel-molybdenum catalyst. Processing conditions are 320℃, 40kg/
a', L) It was ISV-4. Obtained refined oil (A)
was precisely distilled to obtain high quality kerosene with a boiling point range of 166.5-230°C. The properties are shown in Table 1. This oil W
NA was 0.05, V (> T 2zow) was 6.0, and KCDI was 0.45 Te. Also v(≦Te8
or) is 30.0, vA is 8.8, and KSI is 1.
It became 43. Moreover, the sulfur content was below IpP-.
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(’)WNAは0.06、V(>
T 2zo℃)は8.5であり、KCDIは0.61と
なる。またv(51188℃)は30.0. VA ハ
11.7 テあり、KSrは1.42となる。また硫黄
分はlpp園以下であった。Example 2 The refined oil (A) obtained in Example 1 was precision distilled to obtain a fraction with a boiling point range of 164.5 to 230.5°C. Its properties are shown in Table-1. This oil (')WNA is 0.06, V(>
T2zo°C) is 8.5, and KCDI is 0.61. Also, v (51188°C) is 30.0. VA is 11.7 and KSr is 1.42. In addition, the sulfur content was below lpp garden.
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
らに精密蒸留を行い、沸点範囲185.5〜232.5
℃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WNAは0.1 、 V (>72□。℃
)は6.5であり、KCDIは0.59となる。さらに
V(≦T180℃)は27,5、■9は8.0であり、
[81はl、36となる。この浦の硫黄分は1 ppm
以下であった。Example 3 Commercially available Arabian JIS No. 1 kerosene was nuclear-hydrogenated using a platinum catalyst so that the total aromatic content was 10% or less, and further precision distillation was performed to reduce the boiling point range from 185.5 to 232.5.
℃ obtained high quality kerosene. The properties of the obtained oil are shown in Table 1. The WNA of this oil is 0.1, V (>72□.℃
) is 6.5, and KCDI is 0.59. Furthermore, V (≦T180℃) is 27.5, ■9 is 8.0,
[81 becomes l, 36. The sulfur content in this ura is 1 ppm.
It was below.
比較例1〜3
実施例1で示したスマトラ系の精製/1II(A)を精
留せずに用いたもの(比較例1)、精製/d3(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。Comparative Examples 1 to 3 Purification/1II (A) of the Sumatra system shown in Example 1 was used without rectification (Comparative Example 1), Purification/d3 (A) was rectified to remove heavy components. A removed oil (Comparative Example 2) and an oil from which light components of refined oil (A) were removed (Comparative Example 3) were produced.
各試料油の性状を表−1に示す。これらの試料油のKC
DIは各々L、2L O,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
。Table 1 shows the properties of each sample oil. KC of these sample oils
DI is L, 2L O, 45 and 1.74 respectively,
The KSI is 1.52, 1.57 and 1.19, respectively.
比較例4.5
アラビア系の市販JIS 1号灯油(比較例4)と、そ
れを精密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。Comparative Example 4.5 A commercially available Arabian JIS No. 1 kerosene (Comparative Example 4) and a sample oil (Comparative Example 5) were produced by precision distilling it to remove light and heavy components. Table 1 shows the properties of each sample oil.
これらの試料油のKCD lは各々2.66および2.
32となり、KSIは各々1.73と1.62となる。The KCD l of these sample oils were 2.66 and 2.66, respectively.
32, and the KSIs 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段階臭気強度評定尺度
を用いて測定した。結果を表−3に示す。1. Odor sensory test (during handling) An odor sensory test was conducted for each sample oil by 20 subjects assuming the odor during handling. In the test, 80 cc of each sample was placed in a 100 cc glass container with a stopper, the stopper was opened for 10 seconds, the odor of the sample was smelled during the latter 5 seconds, and the odor intensity was evaluated using the 6-level odor intensity rating shown in Table 2. It was measured using a scale. The results are shown in Table-3.
表−2
表−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(松下電器側製)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性の差異は、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aj定した。結果を第1図に示す。Table 2 Table 3 2. Using the sample oils of Stove Combustion Test Examples 1 to 3 and Comparative Examples 1 to 5, a wick up-and-down type stove (manufactured by Matsushita Electric) was used under combustion conditions with the wick scale set to the smallest. , continuous combustion was performed for 1000 hours. Differences in flammability due to differences in fuel are shown by changes in fuel consumption during the combustion period, with the time at the start of combustion set as 100. Furthermore, the degree of dirt on the wick after 1000 hours of combustion was measured using commercially available JIS standards.
Aj was determined as the degree of blackening of the wick in five stages (1 being the least dirty), with No. 1 kerosene being 5. The results are shown in Figure 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 when handled than the kerosene of the comparative example, has a significantly smaller decrease in fuel consumption, and has less blackening of the wick. The degree of combustion was 1 in all cases, demonstrating that the combustibility was good. Furthermore, since the kerosene of the present invention has good flammability, it has been confirmed that it has less odor during ignition and extinguishing than the sample oil of the comparative example, and also has less unburned hydrocarbons and carbon monoxide during steady combustion. did. The kerosene of Comparative Example 2 had a reduction in fuel consumption and the degree of blackening of the wick, which were equivalent to those of the present invention, but the odor during handling was large, and the kerosene of Comparative Example 3
The kerosene has an odor equivalent to that of the present invention when handled, but is significantly inferior in terms of fuel consumption and degree of blackening of the wick.
C発明の効果〕
本発明の高品質灯油は従来の市販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4、
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。C Effects of the Invention] The high-quality kerosene of the present invention has almost no odor when handled compared to the conventional JIS No. 1 commercially available kerosene, and has good flammability, making it a top-bottom type kerosene that is most sensitive to oil properties. Even when used in a stove, the decrease in fuel consumption is extremely small, and the wick is hardly contaminated. Furthermore, the combustion exhaust gas is clean, which is thought to meet the people's desire to lead 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 and degree of blackening of the wick in a stove with an upper and lower wick).
Claims (1)
_2_2_0_℃)で表される灯油燃焼性劣化指数(K
CDI)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(≦T_1_8_0_℃)+1.2
logV_A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。 [式中、W_N_Aは灯油全量に対するナフタレン分の
量(wt%)を、V(>T_2_2_0_℃)は灯油全
量に対する沸点220℃を越える留分の量(vol%)
を、V(≦T_1_8_0_℃)は灯油全量に対する沸
点180℃以下の留分の量(vol%)を、V_Aは灯
油全量に対する芳香族分の量(vol%)をそれぞれ示
す。 〔2〕原油を蒸留して得られるものである請求項1記載
の灯油。[Claims] [1] (1) Formula 1.95W_N_A+0.06V (>T
Kerosene flammability deterioration index (K
CDI) is 1.0 or less, (2) the sulfur content is 1wtppm or less based on the total amount of kerosene, and (3) formula 0.01V (≦T_1_8_0_℃) + 1.2
The kerosene odor index (KSI) expressed as logV_A is 1.
Kerosene characterized by having a concentration of 5 or less. [In the formula, W_N_A is the amount of naphthalene (wt%) based on the total amount of kerosene, and V (>T_2_2_0_℃) is the amount (vol%) of the fraction with a boiling point exceeding 220°C based on the total amount of kerosene.
, V (≦T_1_8_0_°C) represents the amount (vol%) of fractions with a boiling point of 180°C or less relative to the total amount of kerosene, and V_A represents the amount (vol%) of aromatic components relative to the total amount of kerosene. [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 true JPH03182594A (en) | 1991-08-08 |
| JPH0826331B2 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) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| 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 |
| JP2001294874A (en) * | 2000-04-13 | 2001-10-23 | Idemitsu Kosan Co Ltd | Fuel oil for kerosene fuel cells |
| WO2005059062A1 (en) * | 2003-12-19 | 2005-06-30 | Shell Internationale Research Maatschappij B.V., | Kerosene composition |
| WO2006056595A1 (en) * | 2004-11-26 | 2006-06-01 | Shell Internationale Research Maatschappij B.V. | Kerosene compositions |
| JP2006328216A (en) * | 2005-05-26 | 2006-12-07 | Japan Energy Corp | Kerosene composition |
| JP2007031512A (en) * | 2005-07-25 | 2007-02-08 | Cosmo Oil Co Ltd | Kerosene composition |
| JP2008001752A (en) * | 2006-06-20 | 2008-01-10 | Cosmo Oil Co Ltd | Kerosene composition |
| JP2008024840A (en) * | 2006-07-21 | 2008-02-07 | Cosmo Oil Co Ltd | Kerosene composition |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6315889A (en) * | 1986-07-04 | 1988-01-22 | Nippon Petrochem Co Ltd | Production of mixed hydrocarbon 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
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6315889A (en) * | 1986-07-04 | 1988-01-22 | Nippon Petrochem Co Ltd | Production of mixed hydrocarbon solvent |
| JPS63150380A (en) * | 1986-12-13 | 1988-06-23 | Idemitsu Kosan Co Ltd | Improved kerosene |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| 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 |
| JP2001294874A (en) * | 2000-04-13 | 2001-10-23 | Idemitsu Kosan Co Ltd | Fuel oil for kerosene fuel cells |
| WO2005059062A1 (en) * | 2003-12-19 | 2005-06-30 | Shell Internationale Research Maatschappij B.V., | Kerosene composition |
| US7556727B2 (en) | 2003-12-19 | 2009-07-07 | Shell Oil Company | Kerosene composition |
| NO339824B1 (en) * | 2003-12-19 | 2017-02-06 | Shell Int Research | Kerosenblanding |
| WO2006056595A1 (en) * | 2004-11-26 | 2006-06-01 | Shell Internationale Research Maatschappij B.V. | Kerosene compositions |
| JP2006152073A (en) * | 2004-11-26 | 2006-06-15 | Showa Shell Sekiyu Kk | Kerosene composition |
| JP2006328216A (en) * | 2005-05-26 | 2006-12-07 | Japan Energy Corp | Kerosene composition |
| JP2007031512A (en) * | 2005-07-25 | 2007-02-08 | Cosmo Oil Co Ltd | Kerosene composition |
| JP2008001752A (en) * | 2006-06-20 | 2008-01-10 | Cosmo Oil Co Ltd | Kerosene composition |
| JP2008024840A (en) * | 2006-07-21 | 2008-02-07 | Cosmo Oil Co Ltd | Kerosene composition |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0826331B2 (en) | 1996-03-13 |
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