[go: up one dir, main page]

AT116073B - Process for the production of water-soluble products from wool fatty acids. - Google Patents

Process for the production of water-soluble products from wool fatty acids.

Info

Publication number
AT116073B
AT116073B AT116073DA AT116073B AT 116073 B AT116073 B AT 116073B AT 116073D A AT116073D A AT 116073DA AT 116073 B AT116073 B AT 116073B
Authority
AT
Austria
Prior art keywords
water
production
fatty acids
soluble products
wool fatty
Prior art date
Application number
Other languages
German (de)
Original Assignee
Ig Farbenindustrie Ag
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 Ig Farbenindustrie Ag filed Critical Ig Farbenindustrie Ag
Application granted granted Critical
Publication of AT116073B publication Critical patent/AT116073B/en

Links

Landscapes

  • Fats And Perfumes (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Description

  

   <Desc/Clms Page number 1> 
 



  Verfahren zur Herstellung   wasserlöslicher   Produkte aus Wollfettfettsälrell. 
 EMI1.1 
 Phenolen mit sulfurierenden Mitteln behandelt. Solche Produkte zeichnen sieh durch ihre ausgezeichnete peptisierende und schutzkolloide   Wirkung   aus und können darum Verwendung finden zum Emulgieren schwerlöslicher oder unlöslicher Körper und zum Stabilisieren von leicht   ausfallenden Lösungen   wie z. B. denen der 2.   3-Oxynaphtoesäurearylide.   



   Es wurde nun gefunden, dass sich diese schutzkolloiden Eigenschaften dadurch noch wesentlich verbessern lassen, dass man die Wollfettfettsäure vor der Sulfurierung einer Behandlung mit Sauerstoff oder sauerstoffhaltigen Gasen bei erhöhter Temperatur, zweckmässig zwischen 100 und   3000,   unterwirft. Hiebei färbt sich das Ausgangsmaterial dunkler, leichtflüchtige, niedriger molekulare Bestandteile 
 EMI1.2 
 lich, was auf Anhydrisierung   zurückgeführt   werden muss, da die Verseiflmgszahl sich nur wenig ändert. Weiterhin wird die Behandlung auch teilweise Oxydation und Polymerisation der ungesättigten Fettsäuren zur Folge haben. 



   Die Luftbehandlung kann mit oder ohne Zusatz von Katalysatoren, wie harzsaurem Cobalt usw. vorgenommen werden. 



   Beispiel : 200 Gewichtsteile Wollfettfettsäure (Säurezahl   114-2   ; Verseifungszahl 173-8 ; Jodzahl 28-6) werden unter Durchleiten eines lebhaften Luftstromes 8 Stunden auf 2000 Ölbadtemperatur erwärmt. Man erhält 170 Gewichtsteile eines Endproduktes von der   Säurezahl 65-1, Verseifungszahl 157-5   und der Jodzahl   28'4.   



   150 Gewichtsteile des so erhaltenen Produktes werden mit 50 Gewichtsteilen Phenol bei   50-6or   homogenisiert, das Gemisch wird auf 30  abgekühlt, gerührt und im Laufe von 4 Stunden mit 122 Gewichtsteilen Monohydrat versetzt. Die Temperatur soll   350 nieht Übersteigen.   Dann lässt man 300 Gewichtsteile   200/, igues   Oleum bei derselben Temperatur innerhalb 8 Stunden zufliessen, und rührt noch 15-20 Stunden weiter. Eine mit wenig Wasser ausgewaschene Probe muss klar wasserlöslich sein. Man trägt nun auf 150 Gewichtsteile Eis, die Temperatur steigt bis   50 ,   es tritt Trennung in zwei Schichten ein. Die untere Schicht, vom spezifischen Gewicht 1-45 wird abgelassen.

   Zur oberen Schicht gibt man 150 Teile Wasser, löst bei 60  C und fällt mit   Natriumsulfatlösung.   Durch 2-3stündiges Stehenlassen bei   800 tritt wieder   Trennung ein ; die Salzlösung wird abgelassen und das Lösen und Aussalzen wiederholt, bis keine Schwefelsäure mehr vorhanden ist. 



  Dann versetzt man das Rohprodukt mit 5 Gewichtsteilen Butylalkohol und 40   Gewiehtsteilen Natron-   lauge von   30%   Na OR-Gehalt und lässt noch einige Zeit bei   800 stehen,   wobei sieh die letzten Reste von Sulfatlösung als untere Schicht abtrennen. Die obere Schicht ist das Endprodukt, das sich mit schwach saurer Reaktion in heissem Wasser löst. In kaltem Zustand stellt es eine halbfeste, dunkle, butterartige Masse dar. 

**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.



   <Desc / Clms Page number 1>
 



  Process for the production of water-soluble products from wool grease fat.
 EMI1.1
 Phenols treated with sulfurizing agents. Such products are characterized by their excellent peptizing and protective colloid effect and can therefore be used for emulsifying sparingly soluble or insoluble bodies and for stabilizing easily precipitated solutions such. B. those of the 2. 3-Oxynaphtoesäurearylide.



   It has now been found that these protective colloid properties can be significantly improved by subjecting the wool fatty acid to a treatment with oxygen or oxygen-containing gases at an elevated temperature, expediently between 100 and 3000, before sulfurization. The starting material is colored by darker, volatile, lower molecular components
 EMI1.2
 Lich, which has to be attributed to anhydration, since the saponification number changes only slightly. Furthermore, the treatment will also result in partial oxidation and polymerization of the unsaturated fatty acids.



   The air treatment can be carried out with or without the addition of catalysts such as resin-acid cobalt, etc.



   Example: 200 parts by weight of wool fatty acid (acid number 114-2; saponification number 173-8; iodine number 28-6) are heated to an oil bath temperature of 2000 for 8 hours while passing through a brisk stream of air. 170 parts by weight of an end product of acid number 65-1, saponification number 157-5 and iodine number 28'4 are obtained.



   150 parts by weight of the product obtained in this way are homogenized with 50 parts by weight of phenol at 50-6or, the mixture is cooled to 30, stirred and 122 parts by weight of monohydrate are added over the course of 4 hours. The temperature should not exceed 350. Then 300 parts by weight of 200 /, igues oleum are allowed to flow in at the same temperature over the course of 8 hours, and stirring is continued for a further 15-20 hours. A sample washed out with a little water must be clearly soluble in water. Ice is then carried on 150 parts by weight, the temperature rises to 50, and separation into two layers occurs. The lower layer, with a specific gravity of 1-45, is drained.

   150 parts of water are added to the upper layer, which is dissolved at 60 ° C. and precipitated with sodium sulfate solution. By standing at 800 for 2-3 hours, separation occurs again; the salt solution is drained off and the dissolving and salting out repeated until no more sulfuric acid is present.



  Then 5 parts by weight of butyl alcohol and 40 parts by weight of sodium hydroxide solution with 30% Na OR content are added to the crude product and it is left to stand for some time at 800, the last residues of sulfate solution being separated off as the lower layer. The top layer is the end product, which dissolves in hot water with a weakly acidic reaction. When cold, it is a semi-solid, dark, buttery mass.

** WARNING ** End of DESC field may overlap beginning of CLMS **.

 

Claims (1)

PATENT-ANSPRUCH : Abänderung des durch Stammpatent Nr. 113001 geschützten Verfahrens zur Herstellung wasser- löslicher Produkte aus Wollfettfettsäure, dadurch gekennzeichnet, dass die Wollfettfettsäure vor der Sulfierung einer Behandlung mit Sauerstoff oder sauerstoffhaltigen Gasen bei erhöhter Temperatur unterworfen wird. **WARNUNG** Ende CLMS Feld Kannt Anfang DESC uberlappen**. PATENT CLAIM: Modification of the process for the production of water-soluble products from wool fatty acid, which is protected by parent patent no. 113001, characterized in that the wool fatty acid is subjected to a treatment with oxygen or oxygen-containing gases at an elevated temperature before sulfonation. ** WARNING ** End of CLMS field may overlap beginning of DESC **.
AT116073D 1926-12-17 1929-02-02 Process for the production of water-soluble products from wool fatty acids. AT116073B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE113001X 1926-12-17

Publications (1)

Publication Number Publication Date
AT116073B true AT116073B (en) 1930-01-25

Family

ID=5653162

Family Applications (3)

Application Number Title Priority Date Filing Date
AT113001D AT113001B (en) 1926-12-17 1927-12-16 Process for the production of water-soluble products from wool fatty acid.
AT117864D AT117864B (en) 1926-12-17 1928-02-28 Process for the preparation of acidic and alkaline soluble compounds from wool fatty acids.
AT116073D AT116073B (en) 1926-12-17 1929-02-02 Process for the production of water-soluble products from wool fatty acids.

Family Applications Before (2)

Application Number Title Priority Date Filing Date
AT113001D AT113001B (en) 1926-12-17 1927-12-16 Process for the production of water-soluble products from wool fatty acid.
AT117864D AT117864B (en) 1926-12-17 1928-02-28 Process for the preparation of acidic and alkaline soluble compounds from wool fatty acids.

Country Status (1)

Country Link
AT (3) AT113001B (en)

Also Published As

Publication number Publication date
AT113001B (en) 1929-04-25
AT117864B (en) 1930-05-26

Similar Documents

Publication Publication Date Title
AT116073B (en) Process for the production of water-soluble products from wool fatty acids.
DE539625C (en) Process for the production of water-soluble products from wool fatty acids
AT103106B (en) Process for the production of condensation or polymerization products of acetylene.
DE540247C (en) Process for the production of water-soluble products from wool fat
DE531296C (en) Process for the production of water-soluble, in acidic and alkaline solutions soluble products from wool fatty acids
DE491317C (en) Process for the preparation of sulfonic acids from fatty acids aralkylated on the carbon
AT106981B (en) Process for the production of acid-free, pure, resinous condensation products from phenols and aldehydes.
AT105596B (en) Process for the preparation of p-methoxy-o-acetoxybenzoic acid.
AT142027B (en) Process for the preparation of acyl derivatives of the dihydrofollicle hormone.
AT72853B (en) Process for removing the unpleasant smell of fatty acids from tears or fish oils.
AT96831B (en) Process for the simultaneous cleaning and deacidification of oils and fats.
AT128350B (en) Process for the preparation of low-electrolyte aqueous solutions of silk fibroin.
AT100700B (en) Process for the production of phenyl rosindulin.
DE565977C (en) Process for the production of ethers and esters of leuco compounds
AT133915B (en) Process for the preparation of resinous condensation products from aromatic amines and formaldehyde.
AT64479B (en) Process for the production of condensation products from aromatic oxysulfonic acids, which can be used as tanning agents.
DE499051C (en) Process for the preparation of ketones of the anthracene series
DE541316C (en) Process for the preparation of esters or ethers of halogenated carvacroles
AT98708B (en) Process for the preparation of p-aminobenzoic acid esters of 2-methyl-4-diethylamino-pentanol-5, and of 2-methyl-4-dimethylaminopentanol-5.
AT122954B (en) Process for the production of water-soluble condensation products with a tanning effect.
CH147681A (en) Process for the preparation of an aminodiphenylamine derivative.
CH164838A (en) Process for the preparation of 5-chloro-2-amino-1-methoxybenzene-3-sulfonic acid.
CH126194A (en) Process for the preparation of a benzobenzanthronecarboxylic acid.
CH149404A (en) Process for the preparation of a new derivative of ricinoleic acid.
CH171960A (en) Process for the preparation of a dye.