[go: up one dir, main page]

DE1617077A1 - Washing, wetting, emulsifying and dispersing agents - Google Patents

Washing, wetting, emulsifying and dispersing agents

Info

Publication number
DE1617077A1
DE1617077A1 DE19671617077 DE1617077A DE1617077A1 DE 1617077 A1 DE1617077 A1 DE 1617077A1 DE 19671617077 DE19671617077 DE 19671617077 DE 1617077 A DE1617077 A DE 1617077A DE 1617077 A1 DE1617077 A1 DE 1617077A1
Authority
DE
Germany
Prior art keywords
emulsifying
washing
wetting
sodium
dispersing agents
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.)
Pending
Application number
DE19671617077
Other languages
German (de)
Inventor
Ernst Dr Ulsperger
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.)
Berlin Brandenburg Academy of Sciences and Humanities
Original Assignee
Berlin Brandenburg Academy of Sciences and Humanities
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 Berlin Brandenburg Academy of Sciences and Humanities filed Critical Berlin Brandenburg Academy of Sciences and Humanities
Publication of DE1617077A1 publication Critical patent/DE1617077A1/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/42Amino alcohols or amino ethers
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/30Amines; Substituted amines ; Quaternized amines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Description

Wozeh-, Netz--. Emulgier-- und Diaperg:tormittel Die LYtii2d#wg- ba-brJ2f-b die Verwendung grenzflächenak-t#i:vGi# Verbindungen alo Waaoh-9 Nötz-, Ibulgier-und Disperg:Lermittel, Es ist bekannt 9 daß Polyoxyalkylamine der allgemeIneui In der R Aljwl-i R, iit Alk-yl- oder Oxyalkyl und PI.p oleamw1- oder Polyoxyallz82wogite darstellen$ die Ober:fläoheas#pannung ihrer wäßrigen, Lösungen albark herabsetzen und ein starke» Sohauavermögen besitzen, Diese- Verbindungen worden aus Alkyle«uc-#l#-iden und Polyo*.g3raminen hergeatellt, Während Folymwamine verhältnismäne:LE leicht ZUSämSlich Sin49 bereitet die Herstellung von Alkylenoxiden nooh Immer erhebliche teahniaoha f$ohwieriskeite.üo Der Erfindung lag deshalb die Ahegabe zugrunde" als Waßt#ih-. Notz-o Emulgier- und Dispergler# mittel geeignete Vorbindungen zu va-ewonden, deren Aut,-ganGsprodtütte zugänglich sind. werden die aus Glyaidäthern und Amino- . ginWpen tregenden bydrophilen Verbindungen hergeotellten lo*t:Lomsprodukte der allgemeineU yo=ol als W9B0h-p N6tZ-i Eaulgier- und Dispergiermittel verwendete, In der allsämeinen Pormel bedeuten: 402? edrophobe Rest R = Alkylp vorzugsweise C6 bin C -L P, Aryl oder ALilax.-j-L*O Bi und R 2 bedeuten gleiche oder untereahiedliohe ml--,- versohiedenen hydrophilen Gruppen wie Hydrox"i-t Bulto-o Garboxy. oder Amimgruppent aubotituierte aliphatiaobß Restep wobei gegebenenfalls einer der Reste H sein kann, Vorzugsweise wird der Reut vom Taurin$ kletbyltaurin, Ätbmolamlne Diäthanolamin, matbylglucamin, Matbjlmal-lu"amine Aminotri»tb,yl»than.' Diätbylentriamin, Aminosäuren land Eiwo:Lßb,ydrolynaten gebildeto Die Verbindungen zeigen auf Grund der Einführung dea lieteronauerstoffatome in den bjdrophoben Teil den Moleküls besonders vortoilhafte Wanoh-, Netz-p Daulgisr- und Diapergier-Überraschend war" daß d80 VOrhandenaein dieser Verbinduna-en der Oag, allgemeiLen Formel in Waaobmittelkompositionen eine Kalt- und Schnellwäsohe 0:endglioht#- Kloht,- vorausaUBehen war fernerg daß diese Verbindunßea bactoriolde und funsicide Eigenschaften aufweisen und sich somit zum Waschen von Krankenhe.uswäsche beaotdern gut eigUenc, Ven 7orteil ist rerner,- da 8 die verwendeten Verbindungen aus Glyc-,idäthern und den entsprechenden Aminen sehr leicht #erstellbar aindc Langkettige *Uwlglycidäther bä#apielsweinej die nich- vvn den lanßkettigert AMW1enoxiden nur durch daß vorhandenDein eines notoronauerzborfatem in der Kohlenweßeerstoffkotte =tersoliaidibug eim4 'VOrbäJtni-ß"Bals einfach zu- Sängliche Die Erfindung aoll an Hand von BelepieNlen näb r erläutert vordeno Beispiel 18 Reaeptur für ein Schnellwaoobmittels Teile N-(2-edroxy- -lLuMloM -X-meIN ltaurin-matrium 25 Er%Zl) L Natrilmpyrophozphat 10 Natriumtripcl,yphoophat 20 Nat-ri#UMheraMetaphoßphat 5 Carbomymetbj,lcellulose 2 Natriumouitat 33 NagweIumeilikat, 5 Beispiel 21 Rezeptur für ein bleiohenden Grobwenohmltteli 25 Natriump7rophoepbat 15 Natriumcarbonat 15 liegroniumailika0 6 aarbox3methyloallulose 2 Natriumperborat 5 Natriumsulfat 32 Beinpiel 3 3 Reseptur filr ein schnellwaaobMittelg T41.13 25 Natriumtripolzphoophat 30 NatrIUMP7rophoophat 10 Nafflaiumilikat 5 Garb027»,bbyloalluloße 2 Natriumsulrat 28 Beieiel 48 zu 70 S einer aus Ohromlederabfällen gewonneren Au:roebluß-Im4el die ei»n Trookonoubstanzgehalt von etwa 45 bin 50 % - beaitzte läßt man unter RÜoktluJ3 und kräftigen RUhren bei 8&(; langsam 12 g Laurylg17,o:Ldäther nutropfene Sobald vollständige Nomosenie:Lerung der Pb"On OlugOtrOtßu iOtt beendet man die Beaktiont läßt daa Reaktionseemisoh erhalten und reinigt ese Die Reinigung erfolgt duroh Sohütteln den Rohprodukteo mit Inopropanol, wobei zwei Pkwen Oebildet vordene Während die untere Phase zieht =gesetztes Eiweißabbauprodukt entbältg besteht die obere In der Hauptsache aun dem Timeetzungsprodukt von Eiweißabbauprodukt mit dem laur71glycidäther. Nan entfernt den lUohol der oberen Phase und erhält auf diese Weine eine wanohuktive Subets» in Form einer Btwmlöoungg die in einer Wanobflotte (1 Liter) für Baumwollstranggarn wie folgt angewendet wirdt Ohl 6 .Alm. uimoetzmwrodukt aus LuLe.Wozeh-, net-. Emulsifying and diapering agents The LYtii2d # wg- ba-brJ2f-b the use of interfacial ac-t # i: vGi # compounds alo Waaoh-9 Nötz-, Ibulgier- und Disperg: Lermittel, It is known 9 that polyoxyalkylamines are the general In the R Aljwl-i R, iit Alkyl- or Oxyalkyl and PI, Poleamw1- or Polyoxyallz82wogite represent the upper: reducing the surface tension of their aqueous solutions albark and possessing a strong ability to build these compounds from alkyls «Uc- # l # -iden and Polyo * .g3raminen manufactured, while Folymwamine relative: LE easily together with Sin49, the production of alkylene oxides always prepares considerable teahniaoha f $ ohwieriskeite.üo The invention was therefore based on the idea" as Wasst # ih- ... Notz-o emulsifying and Dispergler # Vorbindungen medium suitable to va-ewonden whose Aut, -ganGsprodtütte are accessible, the ginWpen tregenden bydrophilen compounds from Glyaidäthern and amino hergeotellten lo * t: Lomsprodukte the allgemeineU yo = ol as W9B0h-p N6tZ-i Eaulgier- and dispersant used, In the allsämeine Pormel mean: 402? edrophobic radical R = alkylp, preferably C6 bin C- LP, aryl or ALilax.-jL * O Bi and R 2 denote identical or different hydrophilic groups such as hydroxide, Bulto-o Garboxy. or amine groups, substituted aliphaticobß radicals where one of the radicals may optionally be H. Preferably, the Reut from taurine $ kletbyltaurine, Ätbmolamlne diethanolamine, matbylglucamine, Matbjlmal-lu "amine aminotri» tb, yl »than. ' Dietbylenetriamine, amino acids country egg: Lßb, ydrolynaten formed o The compounds show, due to the introduction of the lieteron oxygen atoms in the hydrophobic part of the molecule, particularly advantageous Wanoh-, Netz-p, Daulgisr- and diapergier- surprising was "that d80 existence of these compounds of the Oag , general formula in detergent compositions a cold and quick wash 0: endglioht # - Kloht, - it was also anticipated that these compounds have bactoriolde and funsicidal properties and are therefore well suited for washing hospital laundry, Ven 7orteil is further, - since 8 the compounds used from glycine ethers, iethers and the corresponding amines are very easy to produce as long-chain glycid ethers bä # apielsweinej the non-vn the long-chain AMW1enoxiden only by the fact that there is a notorious orzborfni-breath in the carbon fiber to - Sängliche The invention is based on BelepieNlen b r explains example 18 above Reaction for a quick load by means of parts N- (2-edroxy- -lLuMloM -X-MEIN ltaurine-sodium 25 He% Zl) L Sodium pyrophosphate 10 Sodium triplicate, phosphate 20 Nat-ri # UMheraMetaphoßphat 5 Carbomymetbj, lcellulose 2 Sodium soup 33 NagweIumeilikat, 5 Example 21 Recipe for a leaded coarse owl 25th Sodium proprophoepbate 15 Sodium carbonate 15 liegroniumailika0 6 aarbox3methyloallulose 2 Sodium perborate 5 Sodium sulfate 32 Leg game 3 3 Resepture for a fast weighing medium T41.13 25th Sodium tripolite 30 Sodium proprophophate 10 Nafflaium silicate 5 Garb027 », bbyloalluloße 2 Sodium Sulate 28 For example, 48 to 70 % of an au: roebluß-Im4el obtained from ear leather waste, which has a troublesome content of about 45 % to 50% - is left with stirring and vigorous stirring at 8 %; slowly 12 g of Laurylg17, o: Ldäther nutropfene complete nomosenia : Lerung of Pb "On OlugOtrOtßu IOTT you quit the Beaktiont can daa Reaktionseemisoh receive and cleans ese cleaning takes duroh Sohütteln the Rohprodukteo with Inopropanol, two Pkwen Oebildet vordene While the lower phase draws = set breakdown product of protein entbältg, the upper aun In the main, the Timeetzungsprodukt of protein degradation product with the laur71glycidäther. Nan removes the lUohol the upper phase and obtained in this wines a wanohuktive Subets "in the form of a Btwmlöoungg the wirdt applied follows a Wanobflotte (1 liter) for Baumwollstranggarn as Ohl 6 .alm. uimoetzmwrodukt from Lule .

Natriuwarbonat lo5 « Berseiller Beife 2 6 Beispiel 52 Zum Ausfärben von Baumwollgarng zeBe nIt Indantbrentarbstoffeng bei 60o0 wird eine Farbflotte ver»ndeti, die als Retzmittel 1 6 ja Liter den Beispiel 6 8 Rezeptup für.ein Korrosioneaohutzmittel Teile ölsäure Petroleum 100 L-(ZZ£LdroZZ=3-lLuUlox 1 -diäthatolmün 17 als Baulgator waßser 100 Natriuwarbonat lo5 "Berseiller Beife 2 6 Example 52 to discolouring of Baumwollgarng ZEBE nIt Indantbrentarbstoffeng at 60o0 is a dye liquor ver" Ndeti, as Retz means 1 6 yes 6 liters of the Example 8 Rezeptup für.ein Korrosioneaohutzmittel Parts oleic acid Petroleum 100 L- (ZZ £ LdroZZ = 3-lLuUlox 1 -diethatolmün 17 as a construction agent water 100

Claims (1)

Pataiibanspriioh t, Verwendung von Verbindungen der allgemeinen Pormel der hydrophobe Rest R = Amel,' vorzugewelee 036 biß 03-89 Aryl oder Alkylaryl darstellt und al Und'R2 gleiche oder untersohiedliche mit verschiedenen bydrophilen Gruppe-u## wie Hydroxy-, Sulto-2 Garboxy- oder Aminogruppen, aubstituierte allphatiaohe Reste bedeuten, wobei gegeb--a-3nfalls einer der Reste 11 aein kann2 als WWch--3 Fetz'-, maulzier-. und Diapers:Lerm:LtteloPataiibanspriioh t, use of compounds of the general Pormel the hydrophobic radical R = Amel, 'vorzuewelee 036 to 03-89 represents aryl or alkylaryl and al and'R2 mean the same or different radicals with different hydrophilic groups such as hydroxyl, sulto-2, carboxy or amino groups, substituted allphatiaohe radicals , where, if necessary, one of the residues 11 can be aein2 as WWch - 3 Fetz'-, maulzier-. and Diapers: Lerm: Lttelo
DE19671617077 1967-04-13 1967-04-13 Washing, wetting, emulsifying and dispersing agents Pending DE1617077A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DED0052793 1967-04-13

Publications (1)

Publication Number Publication Date
DE1617077A1 true DE1617077A1 (en) 1971-02-18

Family

ID=7054454

Family Applications (1)

Application Number Title Priority Date Filing Date
DE19671617077 Pending DE1617077A1 (en) 1967-04-13 1967-04-13 Washing, wetting, emulsifying and dispersing agents

Country Status (2)

Country Link
DD (1) DD60382A (en)
DE (1) DE1617077A1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4208345A (en) * 1977-03-01 1980-06-17 Sandoz Ltd. 2-Hydroxy-n-propylamine derivatives useful as surface active agents
EP0367205A1 (en) * 1988-10-31 1990-05-09 Gödecke Aktiengesellschaft 2-Aminocarboxylic acids and their derivatives, methods for their preparation and their use as pharmaceutical compositions
US7737304B2 (en) * 2007-09-28 2010-06-15 Fujifilm Corporation Sulfonic acid polyol compound, polyurethane resin, polyurethane resin for magnetic recording medium, and magnetic recording medium

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4208345A (en) * 1977-03-01 1980-06-17 Sandoz Ltd. 2-Hydroxy-n-propylamine derivatives useful as surface active agents
EP0367205A1 (en) * 1988-10-31 1990-05-09 Gödecke Aktiengesellschaft 2-Aminocarboxylic acids and their derivatives, methods for their preparation and their use as pharmaceutical compositions
WO1990005130A1 (en) * 1988-10-31 1990-05-17 Gödecke Aktiengesellschaft 2-aminocarboxylic acid derivatives, their manufacture and use as drugs
US7737304B2 (en) * 2007-09-28 2010-06-15 Fujifilm Corporation Sulfonic acid polyol compound, polyurethane resin, polyurethane resin for magnetic recording medium, and magnetic recording medium
US7737305B2 (en) * 2007-09-28 2010-06-15 Fujifilm Corporation Sulfonic acid polyol compound, polyurethane resin, polyurethane resin for magnetic recording medium, and magnetic recording medium

Also Published As

Publication number Publication date
DD60382A (en)

Similar Documents

Publication Publication Date Title
DE69512572T2 (en) Tissue paper containing glycerin and quaternary ammonium compounds
EP0043547B1 (en) Fabric softener concentrate
EP0235774B1 (en) Liquid surface-active mixtures
DE3924911C2 (en) Aqueous organosiloxane composition, process for its preparation and its use for the treatment of textiles
EP0082456A2 (en) Concentrated premixes of fabric-softening agents
DE1130956B (en) Amphoteric surfactants and detergents containing quaternary compounds
DE1236517B (en) Process for the preparation of aqueous solutions of oxides of tertiary aliphatic amines
DE1933511A1 (en) Liquid detergent and cleaning agent
DE1617077A1 (en) Washing, wetting, emulsifying and dispersing agents
EP0074078B1 (en) Softening laundry rinser
DE2619668A1 (en) DETERGENT COMPOSITION
DE1469497A1 (en) Textile treatment agents
DE69210411T2 (en) USE OF A TRIETHANOLAMINE PRODUCT BLEND
CH313159A (en) Process for the production of permanent dye and stripping baths
DE2903980A1 (en) Active chlorine-contg. cleansing bleaching and disinfecting compsns. - contain amino-phosphonic acid- or salt- derived amine oxide complexing agent
DE2246907C2 (en) Detergent containing detergent polyamine carboxylates
DE3135013A1 (en) "SOFT SOFT DETERGENT"
DE1074186B (en) cleaning supplies
DE2000432A1 (en) Softeners for fabrics
DE1951156C2 (en) Biocide preparation
DE683845C (en) Wetting agents
DE556772C (en)
DE908008C (en) Method for fulling woolen and blended fabrics
DE1297074B (en) Surface active agents
DE739448C (en) Process for the preparation of ointments containing acylated sulfonamides which are easily absorbed through the skin