JPS603439B2 - Production method of altered oil for combustion test - Google Patents
Production method of altered oil for combustion testInfo
- Publication number
- JPS603439B2 JPS603439B2 JP55032286A JP3228680A JPS603439B2 JP S603439 B2 JPS603439 B2 JP S603439B2 JP 55032286 A JP55032286 A JP 55032286A JP 3228680 A JP3228680 A JP 3228680A JP S603439 B2 JPS603439 B2 JP S603439B2
- Authority
- JP
- Japan
- Prior art keywords
- oil
- altered
- kerosene
- peroxide
- peroxides
- 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
Links
Landscapes
- Liquid Carbonaceous Fuels (AREA)
Description
【発明の詳細な説明】
本発明は、油、特に灯油、自動車用ガソリン航空機用燃
料などの燃料油を酸化反応により変質させた燃焼試験用
変質油の製造法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a modified oil for combustion tests, which is obtained by modifying oil, particularly fuel oil such as kerosene, gasoline for automobiles, and aircraft fuel, through an oxidation reaction.
この種の油を燃料とする燃焼機器の燃焼特性、寿命など
を調べるため、促進試験として変質した燃料油を燃焼さ
せて評価することがある。In order to investigate the combustion characteristics and lifespan of combustion equipment that uses this type of oil as fuel, degraded fuel oil is sometimes burned and evaluated as an accelerated test.
ここに使用される変質油は、従来加熱したり、空気を吹
き込んだり、紫外線を照射したり、あるいは油の劣化す
る環境に暴露させたりする方法により作成されていた。The altered oil used here has traditionally been created by heating, blowing air, irradiating with ultraviolet light, or exposing the oil to an environment that degrades it.
しかし、これらの方法では、いずれも変質油を得るのに
2週間ないし1年以上も要するなど長時間かかる上に、
再現性に乏しく、また任意の変質度のものが得られない
などの欠点があった。燃料油である灯油について、さら
に詳しく説明すると、試験用変質油を得る方法としては
も以下のものが代表的であった。However, all of these methods take a long time, from two weeks to more than a year, to obtain altered oil.
There were drawbacks such as poor reproducibility and inability to obtain a desired degree of alteration. To explain in more detail about kerosene, which is a fuel oil, the following methods were typical for obtaining altered oil for testing.
‘1) 18000以上に加熱して空気を吹し、込む。'1) Heat to 18,000 or more and blow air into it.
‘21 紫外線を照射して空気を吹き込む。御 屋外に
放置する。【1}、■の方法によると、強度の酸価(0
.1以上)の灯油が得られるので、酸価0.01〜0.
03の通常の変質灯油にするため、希釈して試料として
用いられている。'21 Irradiate ultraviolet rays and blow in air. Please leave it outdoors. According to the method of [1} and ■, the strong acid value (0
.. 1 or more) is obtained, so the acid value is 0.01 to 0.
It is diluted and used as a sample in order to make 03 normal degraded kerosene.
‘3}の方法では、灯油の設置場所、暴露日数などを変
える方法が採られる。これらの方法による場合は、変質
させるのに長時間を必要とする上に、作成の都度変質度
が異なるので再現性に乏しく、任意の変質度のものが得
られなかった。Method 3 involves changing the location of kerosene and the number of days of exposure. In the case of these methods, it takes a long time to alter the quality, and the degree of alteration differs each time it is produced, so reproducibility is poor and it is not possible to obtain a product with a desired degree of alteration.
従って、燃焼機器の各種性能を評価するにはきわめて不
都合であった。本発明は、以上のような従来の不都合を
解消し、任意の変質度のものを短時間で、再現性よく製
造する方法を提供するものである。Therefore, it is extremely inconvenient for evaluating various performances of combustion equipment. The present invention eliminates the above-mentioned conventional disadvantages and provides a method for producing products with any degree of deterioration in a short time and with good reproducibility.
本発明は、以下に詳述するように、変質油の分析をはじ
めとして、変質油の生成メカニズムを解明した結果に基
づくもので、油に過酸化物を添加し、油成分と過酸化物
とを反応させることにより、変質油を得るものである。As detailed below, the present invention is based on the results of elucidating the generation mechanism of denatured oil, including analysis of denatured oil. A modified oil is obtained by reacting the
本発明者らは、変質油の生成メカニズムについて検討し
た結果、過酸化物の生成→醸成分の生成→樹脂質の生成
の過程を経ることがわかった。第1表は、正常な市販灯
油と市場で回収した各種経歴の変質灯油について、過酸
化物価、酸価および樹脂質分を測定した結果の例を示す
。1表
第1表から明らかなように、変質灯油は市販の正常灯油
に比較して過酸化物価、酸価、樹脂質いずれも増加して
おり、しかもそれらの値は経歴によってまちまちである
ことがわかる。The present inventors investigated the generation mechanism of altered oil and found that it goes through the following process: generation of peroxides → generation of brewing components → generation of resinous substances. Table 1 shows examples of the results of measuring the peroxide value, acid value, and resin content of normal commercially available kerosene and altered kerosene of various histories recovered from the market. Table 1 As is clear from Table 1, the peroxide value, acid value, and resin content of altered kerosene are higher than that of commercially available normal kerosene, and these values vary depending on the history. Recognize.
上記の事実から、変質灯油を得るには、自然条件に近い
紫外線を照射したり、熱をかけたり、酸素を吹き込んだ
りしなくとも、前記の各劣化成分を添加すればよいと考
えられる。From the above facts, it is considered that in order to obtain degraded kerosene, it is sufficient to add each of the above-mentioned degraded components without irradiating with ultraviolet rays, applying heat, or blowing oxygen under natural conditions.
しかし、各々の成分が十分解明されておらず、しかも一
般の過酸化物が不安定であることなどから「単に劣化成
分を添加するのみでは所望の変質灯油を得ることは困難
である。そこで、本発明者らは、油の劣化が前記のよう
に過酸化物の生成→醸成分の生成→樹脂質の生成という
過程を経ることから、油に過酸化物を添加して反応させ
ることにより、酸成分、樹脂質をも生成させることがで
き、実際に変質したものと同等の変質油を得ることに成
功した。However, since each component is not fully understood and common peroxides are unstable, it is difficult to obtain the desired altered kerosene simply by adding degraded components. The present inventors believe that since oil deterioration goes through the process of peroxide production → brewing component production → resinous production as described above, by adding peroxide to oil and causing a reaction, It was also possible to generate acid components and resinous substances, and succeeded in obtaining denatured oil equivalent to that which had actually denatured.
この方法により変質油を得るには以下の点に注意しなけ
ればならない。【1} 使用する過酸化物の分解生成物
が油に含まれている成分に類似していること。In order to obtain denatured oil by this method, the following points must be noted. [1] The decomposition products of the peroxide used must be similar to the components contained in oil.
‘2) 比較的速やかに分解し終わり、目的の変質油と
なった後は、それ以上油を変質させないこと。'2) Once the oil has been decomposed relatively quickly and has become the desired altered oil, do not allow the oil to deteriorate any further.
剛 油に溶解すること。Hard To dissolve in oil.
などである。etc.
この方法による特徴は以下のとおりである。The features of this method are as follows.
{1} 過酸化物のみを添加して油を劣化させるため、
過酸化物は開始剤となるだけで、他の劣化反応は自然劣
化に近い形で行われる。■ 劣化させるための時間が短
い。{1} To degrade oil by adding only peroxide,
The peroxide only serves as an initiator, and other deterioration reactions occur in a manner similar to natural deterioration. ■ Short time for deterioration.
糊 薬品の添加によるものであるから、再現性に優れる
。Glue Excellent reproducibility as it is made by adding chemicals.
■ 過酸化物の種類および濃度を選ぶことにより、任意
の変質油が得られる。■ Any altered oil can be obtained by selecting the type and concentration of peroxide.
また、過酸化物を添加した後に、加熱したり、紫外線を
照射したり、酸素を吹き込んだりすることにより「さら
に油の変質を容易にすることができる。In addition, after adding peroxide, heating, irradiating with ultraviolet rays, or blowing oxygen can "further facilitate the deterioration of the oil.
本発明に用いられる過酸化物の代表例を以下に挙げる。Representative examples of peroxides used in the present invention are listed below.
舷 ハイド。パーオキサイド類クメンハイドロ/ぐーオ
キサイド、t−ブチルハイドロ/ぐ−オキサイド、【b
} ジアルキルパーオキサイド類
ジーtーブチル/ぐーオキサイド、t−ブチルクミル/
ぐーオキサイド、{C)ジアシルパーオキサィド類
ラウノイル/ぐーオキサイド、3・5・5ートリメチル
ヘキサノイルパーオキサイド、‘d} パーオキシェス
テル類
tーブチル′ぐーオキシアセテ−ト、t−プチルノぐー
オキシラウレート、tーブチル/ぐーオキシ−3151
5ートリメチルヘキサノエート、以下、本発明の実施例
を説明する。Gun Hyde. Peroxides cumene hydro/gu oxide, t-butyl hydro/gu oxide, [b
} Dialkyl peroxides di-t-butyl/gu oxide, t-butylcumyl/
Gu oxide, {C) Diacyl peroxides launoyl/gu oxide, 3,5,5-trimethylhexanoyl peroxide, 'd} Peroxyesters t-butyl'gu oxyacetate, t-butyl nogu oxy Laurate, t-butyl/guoxy-3151
5-trimethylhexanoate Examples of the present invention will be described below.
第2表は各種の過酸化物を市販の正常灯油に1重量%添
加し、8000で4時間反応させた後の過酸化物価等を
比較したものである。Table 2 compares the peroxide values after adding 1% by weight of various peroxides to commercially available normal kerosene and reacting at 8000 for 4 hours.
第2表
第2表の結果から明らかなように、いずれの種類の過酸
化物を用いた場合も灯油は変質する。As is clear from the results in Table 2, kerosene deteriorates when any type of peroxide is used.
しかし、過酸化物の種類によって変質の度合が大きく異
なる。すなわち、ハイドロパーオキサィド類およびジア
ルキルパーオキサイド類を用いた場合は、酸性成分の生
成量が低く、ジアルシルパーオキサィド類を用いた場合
は、酸性成分が比較的多く生成される。パーオキシェス
テル類を用いた場合は三者の劣化成分が共に比較的多く
なっている。次に、過酸化物を添加した後の加熱の効果
および紫外線照射、酸素吹き込みの効果を調べた結果を
説明する。However, the degree of alteration varies greatly depending on the type of peroxide. That is, when hydroperoxides and dialkyl peroxides are used, the amount of acidic components produced is low, and when dialcyl peroxides are used, relatively large amounts of acidic components are produced. When peroxyesters are used, the three deteriorating components are relatively large. Next, the results of investigating the effects of heating, ultraviolet irradiation, and oxygen blowing after adding peroxide will be explained.
過酸化物として、ラウ/ィルパーオキサィド凶および3
・515−トリメチルヘキサノイルパーオキサィド曲を
用いた。As peroxides, lau/il peroxide and 3
- 515-trimethylhexanoyl peroxide music was used.
得られた変質灯油の分析結果を第3表に示す。表中、U
Vは紫外線照射、02は酸素吹き込みを示す。第3表第
3表から、油の変質度合は、過酸化物の添加量の多いほ
ど、加熱温度の高いほど、紫外線を照射するほど、また
酸素を吹き込むほど進行することがわかる。The analysis results of the obtained altered kerosene are shown in Table 3. In the table, U
V indicates ultraviolet irradiation, and 02 indicates oxygen blowing. From Table 3, it can be seen that the degree of oil deterioration progresses as the amount of peroxide added increases, the heating temperature increases, the more ultraviolet rays are irradiated, and the more oxygen is blown into the oil.
なお、第2、3表の分析結果は、室温で3ケ月放置後も
変わらなかった。The analysis results in Tables 2 and 3 remained unchanged even after being left at room temperature for 3 months.
次に、従来の紫外線照射や酸素吹き込みによって変質さ
せた灯油と、本発明により変質させた灯油について、実
際に燃焼機器羊せて特性を比較したところ、変質成分の
対応したものは同様の特性を示し、また、ガスクロマト
グラフィ一、蒸留試験などでも差は認められなかった。Next, we compared the characteristics of kerosene altered by conventional ultraviolet irradiation and oxygen injection and kerosene altered by the present invention using actual combustion equipment, and found that kerosene with corresponding altered components had similar characteristics. Furthermore, no difference was observed in gas chromatography, distillation tests, etc.
従って、本発明の方法により変質させたものも従来法に
よるものとほぼ同一の変質状態になっているものと恩わ
れる。以上の実施例では、灯油について説明したがト本
発明は自動車用ガソリン、航空機用燃料などの燃料油に
も同様に適用することができる。Therefore, it can be said that the material altered by the method of the present invention has almost the same altered state as that obtained by the conventional method. In the above embodiments, kerosene was explained, but the present invention can be similarly applied to fuel oils such as automobile gasoline and aircraft fuel.
Claims (1)
パーオキサイド類、ジアシルパーオキサイド類およびパ
ーオキシエステル類よりなる群から選択される有機過酸
化物を添加して酸化させることを特徴とする燃焼試験用
変質油の製造法。 2 前記酸化反応を熱、光、酸素のいずれかまたは2つ
以上の組合せの条件下で行う特許請求の範囲第1項記載
の燃焼試験用変質油の製造法。[Claims] 1. A fuel oil is oxidized by adding an organic peroxide selected from the group consisting of hydroperoxides, dialkyl peroxides, diacyl peroxides, and peroxy esters to fuel oil. A method for producing altered oil for combustion tests. 2. The method for producing denatured oil for combustion testing according to claim 1, wherein the oxidation reaction is carried out under the conditions of heat, light, oxygen, or a combination of two or more.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55032286A JPS603439B2 (en) | 1980-03-13 | 1980-03-13 | Production method of altered oil for combustion test |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55032286A JPS603439B2 (en) | 1980-03-13 | 1980-03-13 | Production method of altered oil for combustion test |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56129296A JPS56129296A (en) | 1981-10-09 |
| JPS603439B2 true JPS603439B2 (en) | 1985-01-28 |
Family
ID=12354713
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55032286A Expired JPS603439B2 (en) | 1980-03-13 | 1980-03-13 | Production method of altered oil for combustion test |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS603439B2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62186034U (en) * | 1986-05-20 | 1987-11-26 | ||
| JPS62199647U (en) * | 1986-06-11 | 1987-12-19 | ||
| JPS6434526U (en) * | 1987-08-25 | 1989-03-02 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61188493A (en) * | 1985-02-15 | 1986-08-22 | Nippon Mining Co Ltd | Diesel fuel composition |
| JPS6390592A (en) * | 1986-10-06 | 1988-04-21 | Nippon Mining Co Ltd | Fuel composition having high ignitability |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS554160B2 (en) * | 1973-12-18 | 1980-01-29 |
-
1980
- 1980-03-13 JP JP55032286A patent/JPS603439B2/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62186034U (en) * | 1986-05-20 | 1987-11-26 | ||
| JPS62199647U (en) * | 1986-06-11 | 1987-12-19 | ||
| JPS6434526U (en) * | 1987-08-25 | 1989-03-02 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56129296A (en) | 1981-10-09 |
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