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JPS592319B2 - Rubber volatile oil manufacturing method - Google Patents
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JPS592319B2 - Rubber volatile oil manufacturing method - Google Patents

Rubber volatile oil manufacturing method

Info

Publication number
JPS592319B2
JPS592319B2 JP980077A JP980077A JPS592319B2 JP S592319 B2 JPS592319 B2 JP S592319B2 JP 980077 A JP980077 A JP 980077A JP 980077 A JP980077 A JP 980077A JP S592319 B2 JPS592319 B2 JP S592319B2
Authority
JP
Japan
Prior art keywords
volatile oil
fraction
hydrocarbons
rubber volatile
rubber
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
Application number
JP980077A
Other languages
Japanese (ja)
Other versions
JPS5395885A (en
Inventor
俊輔 斉藤
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.)
Eneos Corp
Original Assignee
Mitsubishi Oil 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 Mitsubishi Oil Co Ltd filed Critical Mitsubishi Oil Co Ltd
Priority to JP980077A priority Critical patent/JPS592319B2/en
Publication of JPS5395885A publication Critical patent/JPS5395885A/en
Publication of JPS592319B2 publication Critical patent/JPS592319B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明はゴム揮発油の製造方法に関する。[Detailed description of the invention] The present invention relates to a method for producing rubber volatile oil.

さらに詳しくはナフテン系炭化水素を主成分とし、ベン
ゼン、トルエンおよびキシレン等の芳香族炭化水素の少
ない低毒性のゴム揮発油の製造方法に関する。
More specifically, the present invention relates to a method for producing a low-toxicity rubber volatile oil containing naphthenic hydrocarbons as a main component and containing few aromatic hydrocarbons such as benzene, toluene, and xylene.

従来ゴム揮発油は一般に直留ガソリンの水素化精製物、
直留ガソリンの改質物、直留ガソリンの改質物からベン
ゼン、トルエンおよびキシレン等の芳香族炭化水素をグ
リコール類やスルフオラン等の溶剤で抽出した残油(以
下改質油系芳香族抽出残油という)等を分留し、さらに
アニリン点を調整するため再びこれらにベンゼン、トル
エンおよびキシレンを混入して製造しており、その性状
は一般に沸点範囲が70〜170℃で50℃以下のアニ
リン点を有している。
Traditionally, rubber volatile oil is generally a hydrorefined product of straight-run gasoline,
Reformed straight-run gasoline, residual oil obtained by extracting aromatic hydrocarbons such as benzene, toluene, and xylene from reformed straight-run gasoline with solvents such as glycols and sulfolane (hereinafter referred to as reformed aromatic extracted residual oil) ), etc., and then mixed with benzene, toluene, and xylene again to adjust the aniline point.The product is generally produced with a boiling point range of 70 to 170°C and an aniline point of 50°C or less. are doing.

こSでアニリン点とは溶解力を示す尺度であって、この
値が少さい程溶解力が高いことを示すもので、一般に芳
香族炭化水素はアニリン点が低く、ナフテン系炭化水素
はこれに欠ぎ、パラフィン系炭化水素が最も高いしかる
に最近ベンゼン、トルエンおよびキシレン等の芳香族炭
化水素が人体に悪影響をおよぼすことから、作業環境を
改善するためこれらの含有量の少ないコ弘揮発油の製造
が強く要望されており、特に労働省令の特定化学物質等
障害予防規則テハヘンゼン含有量カ1v01%を超える
ものについて、また回合の有機溶剤中毒予防規則ではト
ルエンとキシレンの合計が5wt%を超えるものについ
て人体への悪影響が重要視され、その取扱いも厳しく制
限されている。
In this S, the aniline point is a scale that indicates the solvency power, and the lower the value, the higher the solvency power. Generally, aromatic hydrocarbons have a low aniline point, and naphthenic hydrocarbons have a low aniline point. However, recently aromatic hydrocarbons such as benzene, toluene, and xylene have a negative effect on the human body, so in order to improve the working environment, Kohiro volatile oil with a low content of these aromatic hydrocarbons has been produced. In particular, the Ministry of Labor Ordinance's Regulations for Prevention of Hazards from Specified Chemical Substances, etc., have a Teha-Hensen content of more than 1v01%, and the Organic Solvent Poisoning Prevention Regulations, which have a total of more than 5wt% of toluene and xylene, have been strongly requested. Due to its negative effects on the human body, its handling is strictly restricted.

従ってこれらの含有量を超えないものでかつアニリン点
50℃以下好ましくはできる限り低いアニリン点のゴム
揮発油の製造が切望されているが従来の製造原料および
製造方法によってこれらの品質を充足させることはでき
ない。
Therefore, it is strongly desired to produce a rubber volatile oil that does not exceed these contents and has an aniline point of 50°C or less, preferably as low as possible, but these qualities cannot be satisfied using conventional production raw materials and production methods. I can't.

すなわち通常のゴム揮発油の沸点範囲である70〜17
0℃留分を対象とすると大部分の直留ガソリンおよび改
質油系芳香族抽出残油等はアニリン点の高いパラフィン
系炭化水素に富んでおりアニリン点が50℃以下のゴム
揮発油を製造するためには、それらにベンゼン、トルエ
ンおよびキシレン等の芳香族炭化水素を多量に混合しな
ければ製造できない。
That is, 70 to 17, which is the boiling point range of normal rubber volatile oil.
Targeting the 0°C fraction, most straight-run gasoline and reformed aromatic extracted residual oil are rich in paraffinic hydrocarbons with a high aniline point, and rubber volatile oil with an aniline point of 50°C or less is produced. In order to do this, it cannot be produced unless a large amount of aromatic hydrocarbons such as benzene, toluene, and xylene are mixed with them.

また芳香族炭化水素に富む直留ガソリンの改質油あるい
はベンゼン、トルエンおよびキシレン等の芳香族炭化水
素の水素添加処理を行ない、これを原料としてナフテン
系炭化水素含有量の多いゴム揮発油を製造する方法もあ
るが芳香族炭化水素に水素添加する際多量の水素を必要
とする他原料自体も高価なため製造コストがかさみ現実
的でない。
We also hydrogenate reformed straight-run gasoline rich in aromatic hydrocarbons or aromatic hydrocarbons such as benzene, toluene, and xylene, and use this as raw material to produce rubber volatile oil with a high naphthenic hydrocarbon content. Although there is a method to do this, it is not practical because it requires a large amount of hydrogen when hydrogenating aromatic hydrocarbons and the raw materials themselves are expensive, increasing production costs.

本発明は上記問題を解決するためになされたもので、炭
化水素油の熱分解によりエチレン、プロピレン等を製造
する際に副成する熱分解ガソリンの水素化精製物から通
常の溶剤抽出操作によって芳香族炭化水素分を分離した
残油を精密蒸留操作によって、ベンゼンが1vo1%以
下、トルエンとキシレンの合計が5wt%以下のナフテ
ン系炭化水素に富むアニリン点が50℃以下のゴム揮発
油を製造する方法である。
The present invention was made in order to solve the above problems, and it is possible to obtain an aromatic aroma by using a conventional solvent extraction operation from the hydrorefined product of pyrolysis gasoline, which is produced as a by-product when producing ethylene, propylene, etc. by pyrolysis of hydrocarbon oil. A rubber volatile oil with an aniline point of 50°C or less, rich in naphthenic hydrocarbons, containing 1 vol% or less of benzene and 5 wt% or less of toluene and xylene in total, is produced by precision distillation of the residual oil from which group hydrocarbons have been separated. It's a method.

すなわち本発明は直留ガソリン等の炭化水素油の熱分解
によってエチレン、プロピレン等を製造する際副成する
熱分解ガソリンを水素化精製したものからグリコール類
やスルフオラン溶剤等を使用する通常の抽出操作によっ
て芳香族炭化水素を除去した抽出残油は主にガソリン製
造、改質油製造及びエチレン製造等の原料となって〜・
るが、この抽出残油には多量のナフテン系炭化水素が含
まれており、かつベンゼン、トルエンおよびキシレン等
の芳香族炭化水素の含有量が僅少であるので、この抽出
残油を精密蒸留操作によって沸点範囲が70〜170℃
で、ベンゼンが1vo1%以下、トルエンとキシレンの
合計が5wt%以下しか含有せず、ナフテン系炭化水素
に富むアニリン点が50℃以下のゴム揮発油を従来法に
比して低価格にて製造することを可能ならしめたもので
ある。
That is, the present invention is a conventional extraction operation using glycols, sulfolane solvents, etc. from hydrorefined pyrolyzed gasoline, which is produced as a by-product when ethylene, propylene, etc. are produced by pyrolysis of hydrocarbon oils such as straight-run gasoline. The extracted residual oil from which aromatic hydrocarbons have been removed is mainly used as a raw material for gasoline production, reformed oil production, ethylene production, etc.
However, this extracted residual oil contains a large amount of naphthenic hydrocarbons, and the content of aromatic hydrocarbons such as benzene, toluene, and xylene is small, so this extracted residual oil is subjected to precision distillation. The boiling point range is 70~170℃
This method produces rubber volatile oil containing less than 1 vol% of benzene, less than 5 wt% of toluene and xylene in total, rich in naphthenic hydrocarbons, and an aniline point of less than 50°C at a lower cost than conventional methods. This made it possible to do so.

次に本発明に使用される水素化精製とは主に炭素数6〜
8の炭化水素留分を第1段階においてはニッケル系触媒
等を使用し第2段階においてはコバルト、モリブデン系
触媒等を使用してオレフィン系炭化水素を水素化し同時
にいおう分等の不純物を除去する方法である。
Next, the hydrorefining used in the present invention mainly refers to
The hydrocarbon fraction No. 8 is hydrogenated using a nickel-based catalyst in the first stage, and a cobalt- or molybdenum-based catalyst in the second stage, while simultaneously removing impurities such as sulfur. It's a method.

また通常の溶剤抽出操作とはベンゼン、トルエンおよび
キシレン等の芳香族炭化水素を溶剤を用いて他の成分か
ら分離するもので溶剤としては=般にはグリコール類、
スルフオラン、アルツルパン等が使用される。
In addition, a normal solvent extraction operation involves separating aromatic hydrocarbons such as benzene, toluene, and xylene from other components using a solvent.
Sulforane, arturpan, etc. are used.

また、精密蒸留操作とは、例えば2本の蒸留塔から構成
される精密蒸留装置により第1塔の塔頂より軟質炭化水
素を除去し、第2塔の塔頂より目的とする沸点範囲のゴ
ム揮発油を製造する操作である。
In addition, precision distillation operation refers to, for example, removing soft hydrocarbons from the top of the first column using a precision distillation apparatus consisting of two distillation columns, and removing soft hydrocarbons from the top of the second column to obtain rubber with a target boiling point range. This is an operation to produce volatile oil.

この場合1本の蒸留塔からなる精密蒸留装置の塔頂およ
び塔底よりそれぞれ軟質炭化水素および重質炭化水素を
除去し、塔央より目的とする沸点範囲のゴム揮発油を製
造しても差支えない。
In this case, it is acceptable to remove soft hydrocarbons and heavy hydrocarbons from the top and bottom of a precision distillation apparatus consisting of one distillation column, respectively, and produce rubber volatile oil with the desired boiling point range from the center of the column. do not have.

またアニリン点50℃以下としたのは50℃を超えると
ゴムの溶解性が悪くなるためである。
Further, the reason why the aniline point is set to be 50°C or lower is that if the temperature exceeds 50°C, the solubility of the rubber deteriorates.

次に本発明の方法で製造されたゴム揮発油を従来方法で
製造されたゴム揮発油と比較すると次表のとおりで、ベ
ンゼン、トルエンおよびキシレン等の芳香族炭化水素の
含有量は僅少となりナフテン系炭化水素は多くアニリン
点の低い溶解力に優れかつ低毒性のゴム揮発油かえられ
ることが解る。
Next, comparing the rubber volatile oil produced by the method of the present invention with the rubber volatile oil produced by the conventional method, the following table shows that the content of aromatic hydrocarbons such as benzene, toluene, and xylene is small, and the content of naphthenes is small. It can be seen that many hydrocarbons have a low aniline point, have excellent dissolving power, and can be used as a low-toxicity substitute for rubber volatile oil.

なお本発明の方法で製造されるゴム揮発油は従来のゴム
揮発油と同じくゴム製品製造用以外にも塗料、接着剤、
抽出、脱脂、農薬、インキ、ドライクリーニング用等の
溶剤として多様な用途に勿論使用されるものである。
The rubber volatile oil produced by the method of the present invention, like conventional rubber volatile oils, can be used not only for manufacturing rubber products but also for paints, adhesives,
Of course, it is used in a variety of applications as a solvent for extraction, degreasing, agricultural chemicals, ink, dry cleaning, etc.

次に本発明の実施の態様についてフローシート図に従っ
てさらに具体的に説明するが本発明はその要旨を越えな
い限り次の実施例に限定されるものではない。
Next, embodiments of the present invention will be described in more detail with reference to flowsheet diagrams, but the present invention is not limited to the following examples unless the gist thereof is exceeded.

図において炭化水素油の直留ガソリンAを熱分解および
蒸留装置1にて処理すると、エチレンプロピレン等の留
分B、熱分解ガソリン留分C1および残査油その他留分
りが分解される。
In the figure, when straight-run gasoline A, which is a hydrocarbon oil, is treated in a pyrolysis and distillation apparatus 1, a fraction B such as ethylene propylene, a pyrolysis gasoline fraction C1, residual oil, and other fractions are decomposed.

この熱分解ガソリン留分Cを更に蒸留装置2にて処理す
ることにより主として炭素数5以下の留分Eと主として
炭素数6〜8の留分Fと主として炭素数9以上の留分G
に分離される。
This pyrolyzed gasoline fraction C is further processed in the distillation apparatus 2 to produce a fraction E mainly having 5 or less carbon atoms, a fraction F mainly having 6 to 8 carbon atoms, and a fraction G mainly having 9 or more carbon atoms.
separated into

主として炭素数6〜8の留分Fを第1次水素化精製装置
3および第2次水素化精製装置4にかげてオレフィン系
炭化水素を水素化してナフテン系炭化水素に富みかつい
おう分等の不純物を除去した留分Hとする。
The fraction F, which mainly has 6 to 8 carbon atoms, is passed through the primary hydrorefining unit 3 and the secondary hydrorefining unit 4 to hydrogenate olefinic hydrocarbons and to obtain fractions rich in naphthenic hydrocarbons, etc. This is referred to as fraction H from which impurities have been removed.

次にこの留分Hをスルフオラン抽出装置5にかげてベン
ゼン、トルエンおよびキシレン等の芳香族炭化水素留分
Iと抽出残油留分Jに分離する。
Next, this fraction H is passed through a sulforane extractor 5 and separated into an aromatic hydrocarbon fraction I such as benzene, toluene and xylene, and an extracted residual oil fraction J.

この抽出残油留分Jを2本の蒸留塔から構成される精密
蒸留装置6および7に導入し6の塔頂より沸点が70℃
以下の留分Kを分離し、7の塔頂より沸点範囲が70〜
170℃の留分りと170℃以上の留分Mとに分離する
This extracted residual oil fraction J is introduced into precision distillation equipment 6 and 7 consisting of two distillation columns, and the boiling point is 70°C from the top of column 6.
The following fraction K is separated, and the boiling point range is 70 to 70 from the top of the column.
It is separated into a fraction at 170°C and a fraction M at 170°C or higher.

この留分りが本発明の方法によってえられたゴム揮発油
である。
This fraction is the rubber volatile oil obtained by the method of the present invention.

【図面の簡単な説明】[Brief explanation of drawings]

図面は本発明の方法の1例を示すフローシート図である
。 1・・・・・熱分解および蒸留装置、2・・・・・・蒸
留装置、3および4・・・・・・水素化精製装置、5・
・・・・・スルフオラン抽出装置、6および7・・・・
・・精密蒸留装置、A・・・・・・原料炭化水素油の直
留ガソリン留分、C・・・・・・熱分解ガソリン留分、
J・・・・・抽出残油留分、L・・・ゴム揮発油留分。
The drawing is a flow sheet diagram showing an example of the method of the present invention. 1...Pyrolysis and distillation device, 2...Distillation device, 3 and 4...Hydrorefining device, 5...
...Sulforane extraction device, 6 and 7...
... Precision distillation equipment, A ... Straight-run gasoline fraction of raw material hydrocarbon oil, C ... Pyrolysis gasoline fraction,
J...Extraction residual oil fraction, L...Rubber volatile oil fraction.

Claims (1)

【特許請求の範囲】[Claims] 1 炭化水素油の熱分解によりエチレン、プロピレン等
を製造する際に副成する熱分解ガソリンの水素化精製物
から通常の溶剤抽出操作によって芳香族炭化水素を分離
した残油を精密蒸留操作によッテヘンセンカ1v01%
以下トルエンとキシレンの合計が5wt%以下のナフテ
ン系炭化水素に富むアニリン点が50℃以下のゴム揮発
油を製造する方法。
1. Aromatic hydrocarbons are separated from the hydrorefined product of pyrolyzed gasoline, which is produced as a by-product when pyrolysis of hydrocarbon oil is produced by pyrolysis, by ordinary solvent extraction, and the residual oil is separated by precision distillation. ttehensenka 1v01%
The following is a method for producing a rubber volatile oil containing a total of toluene and xylene of 5 wt % or less, rich in naphthenic hydrocarbons, and having an aniline point of 50° C. or less.
JP980077A 1977-02-02 1977-02-02 Rubber volatile oil manufacturing method Expired JPS592319B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP980077A JPS592319B2 (en) 1977-02-02 1977-02-02 Rubber volatile oil manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP980077A JPS592319B2 (en) 1977-02-02 1977-02-02 Rubber volatile oil manufacturing method

Publications (2)

Publication Number Publication Date
JPS5395885A JPS5395885A (en) 1978-08-22
JPS592319B2 true JPS592319B2 (en) 1984-01-18

Family

ID=11730261

Family Applications (1)

Application Number Title Priority Date Filing Date
JP980077A Expired JPS592319B2 (en) 1977-02-02 1977-02-02 Rubber volatile oil manufacturing method

Country Status (1)

Country Link
JP (1) JPS592319B2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5556199A (en) * 1978-10-21 1980-04-24 Nippon Petrochemicals Co Ltd Manufacture of hydrocarbon solvent
JPS60114330A (en) * 1983-11-28 1985-06-20 Idemitsu Petrochem Co Ltd Hydrocarbon solvent
JPH0670225B2 (en) * 1985-09-13 1994-09-07 三菱石油株式会社 Method for manufacturing heptane products
JPH0670224B2 (en) * 1988-08-31 1994-09-07 出光興産株式会社 Method for producing petroleum hydrocarbon solvent
CN104164311B (en) * 2014-08-20 2017-05-31 江阴市五洋化工有限公司 Environment-friendly type agent for carbon hydrogen detergent preparation method

Also Published As

Publication number Publication date
JPS5395885A (en) 1978-08-22

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