JPS5945717B2 - Fatty acid production method - Google Patents

Fatty acid production method

Info

Publication number
JPS5945717B2
JPS5945717B2 JP57118018A JP11801882A JPS5945717B2 JP S5945717 B2 JPS5945717 B2 JP S5945717B2 JP 57118018 A JP57118018 A JP 57118018A JP 11801882 A JP11801882 A JP 11801882A JP S5945717 B2 JPS5945717 B2 JP S5945717B2
Authority
JP
Japan
Prior art keywords
fatty acids
fatty acid
production method
acid production
parts
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
JP57118018A
Other languages
Japanese (ja)
Other versions
JPS5915493A (en
Inventor
典正 藤花
茂 横山
盛「つぐ」 大洞
行雄 藤井
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.)
TOEI KEMIKARU KK
Original Assignee
TOEI KEMIKARU KK
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 TOEI KEMIKARU KK filed Critical TOEI KEMIKARU KK
Priority to JP57118018A priority Critical patent/JPS5945717B2/en
Publication of JPS5915493A publication Critical patent/JPS5915493A/en
Publication of JPS5945717B2 publication Critical patent/JPS5945717B2/en
Expired legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/74Recovery of fats, fatty oils, fatty acids or other fatty substances, e.g. lanolin or waxes

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  • Fats And Perfumes (AREA)

Description

【発明の詳細な説明】 この発明は、脂肪酸に係るものであつて、動植物性油脂
のアルカリ油脂(以下、フーツという)から脂肪酸を工
業的に有利に収得することを目的とする。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to fatty acids, and an object of the present invention is to industrially advantageously obtain fatty acids from alkaline fats and oils of animal and vegetable origin (hereinafter referred to as "fats").

フーツは、アルカリ石鹸を主材としこれとグリセラード
と夾雑物との混合物であるから、これから(了ルカリ石
鹸及びグリセラードを構成する)脂肪酸を良質の姿でか
つ工業的に有利に収得することが当業者の評題である。
Futs is a mixture of alkaline soap and glycerade and impurities, so it is necessary to obtain fatty acids (constituting alkaline soap and glycerade) in good quality and industrially advantageously. This is the company's evaluation.

このような脂肪酸収得の方法としては、多くが知られて
いるが、この方法は、2大別される。
Although many methods for obtaining fatty acids are known, these methods can be broadly classified into two.

その1は、アルカリの添加下に常圧もしくは加圧下に鹸
化しついで硫酸を使用して中和分解するという方法(例
えば、特開昭49−124103)であり、他は、フー
ツを硫酸により中和分解して得る所謂ダーク油に水を加
え触媒を用い又は用いずに加圧下に加水分解させるかも
しくはトイツツエル分解させるというもの(例えば、油
化学第19巻第8号P、808)である。これら既知の
方法には何れも欠点がある。
The first method is to saponify the foot under normal pressure or increased pressure with the addition of an alkali, and then neutralize and decompose it using sulfuric acid (for example, JP-A-49-124103). Water is added to the so-called dark oil obtained by sumolysis, and the oil is hydrolyzed under pressure with or without a catalyst, or it is subjected to Teutzzer decomposition (for example, Yukagaku Vol. 19, No. 8, P, 808). All of these known methods have drawbacks.

前者の方法によると、アルカリの使用量が多過ぎること
、アルカリの中和剤を多量に要すること等であり、後者
の方法によると、収得脂肪酸を原料とする商品例えば化
粧石鹸に着色現象を生ずること、更に製造工程が複雑で
生産効率が低いこと等である。この発明は、このような
欠点を有しないものであつて、以下にその詳細を説明す
る。
According to the former method, too much alkali is used and a large amount of alkali neutralizing agent is required, and when the latter method is used, products made from the obtained fatty acids, such as cosmetic soaps, may be colored. Furthermore, the manufacturing process is complicated and production efficiency is low. The present invention does not have such drawbacks and will be described in detail below.

まず、出発原料は、フーーツである。First, the starting material is foods.

既述のように、フーツは、牛脂、豚脂、菜種油、大豆油
、綿実油、糖油、とうもろこし油、その他の動植物性油
脂をアルカリ精製するとき副産物として取除かれる所謂
滓部分である。フーツを加熱加圧下におき、含有するグ
リセラードを加水分解して脂肪酸とグリセリンを生成さ
せる。
As mentioned above, foots are the so-called dregs that are removed as a by-product during alkali refining of beef tallow, lard, rapeseed oil, soybean oil, cottonseed oil, sugar oil, corn oil, and other animal and vegetable oils and fats. The foots are placed under heat and pressure to hydrolyze the glycerade they contain to produce fatty acids and glycerin.

この際、油脂の起源の如何によつて若干異なるが、用い
る圧力は約7〜35に’/crltでよく、温度は約1
70〜240℃でよい。反応が温度約170℃・圧力約
7に、/CTlt以下では進みにくく、約240℃・
35に’/crlt以上では高度不飽和脂肪酸の変質、
脂肪酸の重合その他の悪作用が起る。この反応には触媒
例えばアルカリ類は添加しない。これがこの発明の特長
である。生成した脂肪酸とグリセリンと残留するナトリ
ヘウム石鹸との混合系に特定の溶剤と鉱酸を添加する。
At this time, the pressure used may vary slightly depending on the origin of the fat or oil, but the pressure used may be approximately 7 to 35'/crlt, and the temperature may be approximately 1
The temperature may be 70 to 240°C. The reaction does not proceed at a temperature of about 170°C and a pressure of about 7, or below /CTlt, and at a temperature of about 240°C.
Above 35'/crlt, polyunsaturated fatty acids are altered,
Polymerization of fatty acids and other adverse effects occur. No catalysts such as alkalis are added to this reaction. This is the feature of this invention. A specific solvent and mineral acid are added to the mixed system of the produced fatty acids, glycerin, and residual sodium soap.

溶剤を特定することがこの発明の特長である。The feature of this invention is to specify the solvent.

くわしくは、それはケトン類(例えば、アセトン、ME
K..MIBKlメチルプロピルケトン、ジエチルケト
ンその他)50〜90%(重量、以下同じ)とC69の
炭化水素(例えば、ベンゼン、トルエン、キシレンヘキ
サン、その他)50〜10%からなる均質系である。こ
の際ケトン類が50%以下のときは、反応終了系につい
て生成した脂肪酸と芒硝ないし食塩を含む水との分離が
不充分になり、90%以上のときは、収得脂肪酸の純度
が悪くなる。しかしてこの溶剤はフーツにたいし半量な
いし倍量使用する。この系には鉱酸例えば硫酸、塩酸を
存在させる。
Specifically, it refers to ketones (e.g. acetone, ME
K. .. MIBKl is a homogeneous system consisting of 50 to 90% (by weight, the same applies hereafter) (methyl propyl ketone, diethyl ketone, etc.) and 50 to 10% C69 hydrocarbons (for example, benzene, toluene, xylene hexane, etc.). At this time, when the ketones content is less than 50%, separation of the fatty acid produced in the reaction-completed system from water containing mirabilite or common salt becomes insufficient, and when it is more than 90%, the purity of the obtained fatty acid becomes poor. However, use half or double the amount of solvent for the foots. A mineral acid such as sulfuric acid or hydrochloric acid is present in this system.

その使用量は、反応系の反応終了時についてそのPHが
4以下にするに足りるものでよい。鉱酸は、反応系中、
ナトリウム石鹸のNaと結合して芒硝または食塩になり
脂肪酸から遊離する。この処理は常圧下、約60〜75
℃の温度において行なわれるO反応完了系は生成脂肪酸
の溶剤溶液層と芒硝または食塩とグリセリンを含む水層
と中間層(その成分組成は原料の違いによつて種々にな
るが、水を主とし、これに芒硝等と脂肪酸と溶剤、夾雑
物の混合系)の3層を形成する。
The amount used may be sufficient to bring the pH of the reaction system to 4 or less at the end of the reaction. In the reaction system, the mineral acid
It combines with Na in sodium soap to form mirabilite or common salt and is released from fatty acids. This treatment is carried out under normal pressure, about 60 to 75
The O reaction completion system, which is carried out at a temperature of , and on top of this, three layers of mirabilite, etc., fatty acids, solvents, and a mixture of impurities) are formed.

これから常法により脂肪酸のみを単離する。From this, only fatty acids are isolated using conventional methods.

ここにこの発明はその目的を達し了える。この発明の作
用、効果の主なものを説明すると、1ソーダ類、鉱酸類
の使用量が従来法に較べて格段に少い。
This invention has now achieved its purpose. To explain the main functions and effects of this invention, the amount of soda and mineral acids used is much smaller than in the conventional method.

その故は、フーツをそのま\加圧、加熱下に分解するか
ら、従来法のような鹸化反応を必要としない、鉱酸はフ
ーツ中に存在するナトリウム石鹸中のNa当量で足りる
とするからである。2溶剤は混合系を使用するから、ケ
トン類単独使用の場合(例えば、特公昭42−2764
7、同43−2718)に比べて、生成脂肪酸層をより
明確に層分離させることができ、つれて、品質の向上し
た目的物が得られる。
This is because the foots are decomposed as they are under pressure and heat, so there is no need for a saponification reaction like in conventional methods.The mineral acid is sufficient as the Na equivalent in the sodium soap present in the foots. It is. Since a mixed system of two solvents is used, when ketones are used alone (for example, Japanese Patent Publication No. 42-2764
7, 43-2718), the resulting fatty acid layer can be separated more clearly, and as a result, a target product with improved quality can be obtained.

実施例 1 グリセラード12.5(f)、ナトリウム石鹸19.4
%、水分その他68.0%よりなる大豆系フーツ、10
0部(重量、以下同じ)をオートクレーブ中で180℃
・8Kf/0I下に3時間加熱し、加水分解を行なつた
Example 1 Glycerade 12.5(f), Sodium Soap 19.4
%, moisture and other 68.0% soybean food, 10
0 parts (weight, same below) in an autoclave at 180℃
- Hydrolysis was carried out by heating at 8Kf/0I for 3 hours.

生成物は、グリセラード0.6%、脂肪酸11.5%、
ナトリウム石鹸19.4%、グリセリン1.26%、水
その他67.2%よりなるものであつた。このものにM
EK44.4部、ベンゼン8.6部からなる混合溶剤を
加える。
The product contains 0.6% glycerade, 11.5% fatty acids,
It consisted of 19.4% sodium soap, 1.26% glycerin, and 67.2% other water. M for this thing
A mixed solvent consisting of 44.4 parts of EK and 8.6 parts of benzene is added.

さらに70%硫酸8部を加えて、7『C・60分間かき
まぜた。系のPHは3.5であつた。これを60分間常
温下に放置したところ、上から脂肪酸を含む溶剤層、中
間層、芒硝、グリセリンを含む下層の3層に明確に分離
した。最上層部を単離し、これから溶剤を蒸発させて粗
脂肪酸29.8部(脂肪酸98(!))を得た。
Further, 8 parts of 70% sulfuric acid was added and stirred for 60 minutes at 7'C. The pH of the system was 3.5. When this was left at room temperature for 60 minutes, it was clearly separated into three layers: a solvent layer containing fatty acids, an intermediate layer, and a lower layer containing Glauber's salt and glycerin. The top layer was isolated and the solvent was evaporated from it to obtain 29.8 parts of crude fatty acids (98(!) fatty acids).

実施例 2菜種油からのフーツ300部をオートクレー
ブ中で、220℃・24Kf/C!t下に3時間加熱し
、加水分解を行なつた。
Example 2 300 parts of foods made from rapeseed oil were placed in an autoclave at 220°C and 24Kf/C! Hydrolysis was carried out by heating for 3 hours under t.

生成物にMIBKlベンゼン混合溶剤(85:15比)
195部と硫酸179を加えて、70℃・60分間かき
まぜた。系のPHは3.1であつた。系は3層に明確に
分離した。上層液から溶剤を回収し、粗脂肪酸93部を
得た。粗脂肪酸の品質は、中和価188.4、鹸化価1
98.7、ヨウ素価121.4(分解率94.8%)で
あつた。
MIBKl benzene mixed solvent (85:15 ratio) to the product
195 parts and 179 parts of sulfuric acid were added and stirred at 70°C for 60 minutes. The pH of the system was 3.1. The system was clearly separated into three layers. The solvent was recovered from the upper layer liquid to obtain 93 parts of crude fatty acid. The quality of crude fatty acids is neutralization value 188.4, saponification value 1
The iodine value was 98.7 and the iodine value was 121.4 (decomposition rate 94.8%).

Claims (1)

【特許請求の範囲】[Claims] 1 動植物性油脂のフーツを約170〜240℃、約7
〜35Kg/cm^2下に加水分解し、ついで約60〜
75℃の温度下にこれにケトン類約50〜90%とC_
6〜_9の炭化水素約50〜10%との混合溶剤とフー
ツ中のナトリウム含有量当量以上の鉱酸とを添加して系
のPHを4以下にすることを特長とする脂肪酸の製法。
1 Heat animal and vegetable oils and fats at about 170 to 240℃, about 7
~ Hydrolyzed to below 35Kg/cm^2, then approximately 60~
Approximately 50-90% of ketones and C_
A method for producing fatty acids characterized by adding a mixed solvent with about 50 to 10% of a hydrocarbon of 6 to _9 and a mineral acid having an amount equivalent to or more than the sodium content in foots to bring the pH of the system to 4 or less.
JP57118018A 1982-07-06 1982-07-06 Fatty acid production method Expired JPS5945717B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57118018A JPS5945717B2 (en) 1982-07-06 1982-07-06 Fatty acid production method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57118018A JPS5945717B2 (en) 1982-07-06 1982-07-06 Fatty acid production method

Publications (2)

Publication Number Publication Date
JPS5915493A JPS5915493A (en) 1984-01-26
JPS5945717B2 true JPS5945717B2 (en) 1984-11-08

Family

ID=14726021

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57118018A Expired JPS5945717B2 (en) 1982-07-06 1982-07-06 Fatty acid production method

Country Status (1)

Country Link
JP (1) JPS5945717B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6169893A (en) * 1984-08-29 1986-04-10 ジエイグル−プ エス ギル Regnerative utilization of sewage floating scum

Also Published As

Publication number Publication date
JPS5915493A (en) 1984-01-26

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