CH203858A - Process for the production of a valuable highly capillary-active substance. - Google Patents

Process for the production of a valuable highly capillary-active substance.

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Publication number
CH203858A
CH203858A CH203858DA CH203858A CH 203858 A CH203858 A CH 203858A CH 203858D A CH203858D A CH 203858DA CH 203858 A CH203858 A CH 203858A
Authority
CH
Switzerland
Prior art keywords
propane
sodium
acid
reaction
chloro
Prior art date
Application number
Other languages
German (de)
Inventor
A-G Friedrich Steinfels
Original Assignee
Friedrich Steinfels A G
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 Friedrich Steinfels A G filed Critical Friedrich Steinfels A G
Publication of CH203858A publication Critical patent/CH203858A/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K23/00Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
    • C09K23/02Alkyl sulfonates or sulfuric acid ester salts derived from monohydric alcohols
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K23/00Use of substances as emulsifying, wetting, dispersing, or foam-producing agents

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Detergent Compositions (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Description

  

  



  Verfahren zur Herstellung eines wertvollen   hochkapillaraktiven    Stoffes.



   Zur Herstellung eines wertvollen hochkapillaraktiven Stoffes kann nach dem Hauptpatent durch Umsetzung von 3-chlor2-oxy-propan-1-sulfonsaurem Natrium mit Kaliumstearat intermediÏr gebildetes 2,3oxido-propan-1-sulfonsaures Natrium mit dem bei   dieserUnisetzunggleichzeitigfrei-    gewordenen Stearin zu einem bei der Verar  beitung    von Textilien n tzlichen Endstoff umgesetzt werden. Gemäss dem vorliegenden   Verfaihren wird    an Stelle des   ga. liumstearats    ein Alkalisalz der technischen ÍlsÏure verwendet. Das Produkt zeichnet sich durch ein    hervorra, gend, es Netz-, Waseh-, Reinigungs-, Emulgier-und Dispergiervermogen und    durch eine ebensolche SÏure-, Bittersalz- und   Kalkbeständigkeit a. us.   



   Nach einem Ausführungsbeispiel des Verfahrens werden in 27 Teile erwÏrmte   technische OLsäure unter Rühren    5,   3    Teile kalzinierte Soda. oder ein anderes, die   Neu-      tra. lisa. tion bewirkendes Alkali    in   entspre-      chender Menge allmählich eingebtraoht    und   mach    Aufhören der   Gasentwieklung    bei 140 bis   M5   C 20 Teile wasserfreies 3-Chlor-2-    oxy-propan-1-sulfonsaures Natrium zugef gt.



  Nach gutem Durchmischen wird die Masse so lange   auf'dieserTempera-targelia,lten,    bis   eine titrierte Probe da, s Ende der Reaktion    anzeigt. Bei der Reaktion des 3-Chlor-2-oxypropan-1-sulfonsauren Natriums mit dem   Alkal. isalz    der ÍlsÏure wird 2,3-oxido-propan-1-sulfonsaures Natrium intermediÏr gebild, und gleichzeitig mit der freiwerdenden ÍlsÏ ure zum   Endstoff Timgesetzt. Dieser    kann durch kochenden Alkohol vom Kochsalz. getrennt und aus der Spritl¯sung, gegebenenfalls nach EntfÏrben mit Kohle, als farbloses Pulver erhalten werden. Dieses gibt mit Wasser   stark schäumende, kalk-und      säureunempfindliehe,    klare   Losungen.     



   PATENTANSPRUCH :
Verfahren zur   Eerstellungeines,wertvol-    len hochkapillaraktiven Stoffes, dadurch gekennzeichnet, da¯ durch Umsetzung von 3 

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





  



  Process for the production of a valuable highly capillary-active substance.



   According to the main patent, by reacting sodium 3-chloro-oxy-propane-1-sulphonic acid with potassium stearate, sodium 2,3oxido-propane-1-sulphonic acid formed as an intermediate with the stearin released at the same time during this dissolution can be used to produce a valuable substance with high capillary activity Processing of textiles useful end material can be implemented. According to the present procedure, instead of the ga. lium stearate is an alkali salt of technical Ísure used. The product is characterized by excellent wetting, washing, cleaning, emulsifying and dispersing properties and by its resistance to acids, Epsom salts and lime a. us.



   According to one exemplary embodiment of the process, 5.3 parts of calcined soda are added to 27 parts of heated technical grade acid with stirring. or another, the neutra. Lisa. Gradually add the appropriate amount of alkali causing the reaction and add 20 parts of anhydrous sodium 3-chloro-2-oxy-propane-1-sulphonic acid to stop the evolution of gas at 140 to M5 C.



  After thorough mixing, the mass is kept on this tempera-targelia, until a titrated sample indicates the end of the reaction. In the reaction of 3-chloro-2-oxypropane-1-sulfonic acid sodium with the alkali. The oleic acid salt is formed as an intermediate 2,3-oxido-propane-1-sulfonic acid sodium, and at the same time, with the released oleic acid, it is converted into the end product Tim. This can be achieved by boiling alcohol from the table salt. separated and obtained from the Spritl¯sung, optionally after decolorization with charcoal, as a colorless powder. This gives strongly foaming, lime and acid-insensitive, clear solutions with water.



   PATENT CLAIM:
Process for the production of a valuable highly capillary-active substance, characterized in that by converting 3

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



 

Claims (1)

**WARNUNG** Anfang CLMS Feld konnte Ende DESC uberlappen **. ** WARNING ** Beginning of CLMS field could overlap end of DESC **. Verfahren zur Herstellung eines wertvollen hochkapillaraktiven Stoffes. Process for the production of a valuable highly capillary-active substance. Zur Herstellung eines wertvollen hochkapillaraktiven Stoffes kann nach dem Hauptpatent durch Umsetzung von 3-chlor2-oxy-propan-1-sulfonsaurem Natrium mit Kaliumstearat intermediÏr gebildetes 2,3oxido-propan-1-sulfonsaures Natrium mit dem bei dieserUnisetzunggleichzeitigfrei- gewordenen Stearin zu einem bei der Verar beitung von Textilien n tzlichen Endstoff umgesetzt werden. Gemäss dem vorliegenden Verfaihren wird an Stelle des ga. liumstearats ein Alkalisalz der technischen ÍlsÏure verwendet. Das Produkt zeichnet sich durch ein hervorra, gend, es Netz-, Waseh-, Reinigungs-, Emulgier-und Dispergiervermogen und durch eine ebensolche SÏure-, Bittersalz- und Kalkbeständigkeit a. us. According to the main patent, by reacting sodium 3-chloro-oxy-propane-1-sulphonic acid with potassium stearate, sodium 2,3oxido-propane-1-sulphonic acid formed as an intermediate with the stearin released at the same time during this dissolution can be used to produce a valuable substance with high capillary activity Processing of textiles useful end material can be implemented. According to the present procedure, instead of the ga. lium stearate is an alkali salt of technical Ísure used. The product is characterized by excellent wetting, washing, cleaning, emulsifying and dispersing properties and by its resistance to acids, Epsom salts and lime a. us. Nach einem Ausführungsbeispiel des Verfahrens werden in 27 Teile erwÏrmte technische OLsäure unter Rühren 5, 3 Teile kalzinierte Soda. oder ein anderes, die Neu- tra. lisa. tion bewirkendes Alkali in entspre- chender Menge allmählich eingebtraoht und mach Aufhören der Gasentwieklung bei 140 bis M5 C 20 Teile wasserfreies 3-Chlor-2- oxy-propan-1-sulfonsaures Natrium zugef gt. According to one exemplary embodiment of the process, 5.3 parts of calcined soda are added to 27 parts of heated technical grade acid with stirring. or another, the neutra. Lisa. Gradually add the appropriate amount of alkali causing the reaction and add 20 parts of anhydrous sodium 3-chloro-2-oxy-propane-1-sulphonic acid to stop the evolution of gas at 140 to M5 C. Nach gutem Durchmischen wird die Masse so lange auf'dieserTempera-targelia,lten, bis eine titrierte Probe da, s Ende der Reaktion anzeigt. Bei der Reaktion des 3-Chlor-2-oxypropan-1-sulfonsauren Natriums mit dem Alkal. isalz der ÍlsÏure wird 2,3-oxido-propan-1-sulfonsaures Natrium intermediÏr gebild, und gleichzeitig mit der freiwerdenden ÍlsÏ ure zum Endstoff Timgesetzt. Dieser kann durch kochenden Alkohol vom Kochsalz. getrennt und aus der Spritl¯sung, gegebenenfalls nach EntfÏrben mit Kohle, als farbloses Pulver erhalten werden. Dieses gibt mit Wasser stark schäumende, kalk-und säureunempfindliehe, klare Losungen. After thorough mixing, the mass is kept on this tempera-targelia, until a titrated sample indicates the end of the reaction. In the reaction of 3-chloro-2-oxypropane-1-sulfonic acid sodium with the alkali. The oleic acid salt is formed as an intermediate 2,3-oxido-propane-1-sulfonic acid sodium, and at the same time, with the released oleic acid, it is converted into the end product Tim. This can be achieved by boiling alcohol from the table salt. separated and obtained from the Spritl¯sung, optionally after decolorization with charcoal, as a colorless powder. This gives strongly foaming, lime- and acid-insensitive, clear solutions with water. PATENTANSPRUCH : Verfahren zur Eerstellungeines,wertvol- len hochkapillaraktiven Stoffes, dadurch gekennzeichnet, da¯ durch Umsetzung von 3 chlor-2-oxy-propan-1-sulfonsaurem Natrium mit einem Alkalisalz der technischen Olsäure intermediÏr gebildetes 2,3-oxido-propan-1 sulfonsaures Natrium mit der bei dieser Um- setzung gleichzeitig freigewordenen Olsäure umgesetzt wird. PATENT CLAIM: Process for the preparation of a valuable, highly capillary-active substance, characterized in that 2,3-oxido-propane-1-sulfonic acid sodium formed as an intermediate by reaction of 3 chloro-2-oxy-propane-1-sulfonic acid sodium with an alkali salt of technical oleic acid is reacted with the oleic acid released at the same time during this reaction. Der Endstoff hat ein hervorragendes Netz-, Wasch-, Reinigungs-, Emulgier-und Dispergiervermögenund'eine'e.hensolche SÏure-, Bittersalz und KalkbestÏndigkeit. The end product has excellent wetting, washing, cleaning, emulsifying and dispersing properties and is also resistant to acids, Epsom salts and lime.
CH203858D 1935-11-05 1936-10-02 Process for the production of a valuable highly capillary-active substance. CH203858A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE203858X 1935-11-05
CH195069T 1936-10-02

Publications (1)

Publication Number Publication Date
CH203858A true CH203858A (en) 1939-03-31

Family

ID=25722718

Family Applications (1)

Application Number Title Priority Date Filing Date
CH203858D CH203858A (en) 1935-11-05 1936-10-02 Process for the production of a valuable highly capillary-active substance.

Country Status (1)

Country Link
CH (1) CH203858A (en)

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