DE1129255B - Emulsifiable textile oil - Google Patents
Emulsifiable textile oilInfo
- Publication number
- DE1129255B DE1129255B DES43220A DES0043220A DE1129255B DE 1129255 B DE1129255 B DE 1129255B DE S43220 A DES43220 A DE S43220A DE S0043220 A DES0043220 A DE S0043220A DE 1129255 B DE1129255 B DE 1129255B
- Authority
- DE
- Germany
- Prior art keywords
- oil
- emulsifiable
- oil according
- soluble
- emulsifier
- 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
Links
Classifications
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
- D06M13/432—Urea, thiourea or derivatives thereof, e.g. biurets; Urea-inclusion compounds; Dicyanamides; Carbodiimides; Guanidines, e.g. dicyandiamides
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/017—Mixtures of compounds
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- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M7/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
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- C10N2010/02—Groups 1 or 11
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/46—Textile oils
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/40—Reduced friction resistance, lubricant properties; Sizing compositions
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- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S260/00—Chemistry of carbon compounds
- Y10S260/15—Antistatic agents not otherwise provided for
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Lubricants (AREA)
Description
DEUTSCHESGERMAN
PATENTAMTPATENT OFFICE
S 43220 IVc/29 bS 43220 IVc / 29 b
ANMELDETAG: 28. MÄRZ 1955 REGISTRATION DATE: MARCH 28, 1955
BEKANNTMACHUNG
DER ANMELDUNG
UNDAUSGABEDER
AUSLEGESCHRIFT: 10. MAI 1962 NOTICE
THE REGISTRATION
ANDOUTPUTE
EDITORIAL: MAY 10, 1962
Vor der mechanischen Behandlung von Textilfasern, Garnen, Fäden, Zwirnen u. dgl., ζ. Β. dem Krempeln, Spinnen, Winden und Stricken, ist es üblich, ein Schmälzmittel auf das Gut aufzubringen, welches die Fasern während des Hindurchlaufens durch die Maschine schützt und schmiert und das anschließend durch Spülen, z. B. in wäßriger Seifenlösung, wieder entfernt werden kann.Before the mechanical treatment of textile fibers, yarns, threads, twisted threads and the like, ζ. Β. the card, Spinning, winding and knitting, it is customary to apply a lubricant to the goods which the Protects and lubricates fibers as they pass through the machine and that afterwards by rinsing, e.g. B. in aqueous soap solution, can be removed again.
In der Praxis haben sich nicht alle empfohlenen Schmälzmittel als befriedigend erwiesen. Aus der britischen Patentschrift 703 499 ist es bekannt, mineralische Ölzusammensetzungen als Schmälze zu verwenden, welche eine öllösliche Oxyverbindung und eine organische Verbindung mit dem Rest Emulgierbares TextilölIn practice, not all recommended lubricants have proven to be satisfactory. From the British patent specification 703 499 it is known to use mineral oil compositions as smear, which is an oil-soluble oxy compound and an organic compound with the rest Emulsifiable textile oil
R ■ Χ™ ■ C νR ■ Χ ™ ■ C ν
,N-, N-
N =N =
enthalten. Hierin ist R ein organischer Rest, X ein Sauerstoff- oder Schwefelatom oder eine Iminogruppe, und m ist Null oder Eins. Mit solchen Zusammensetzungen sollen die elektrischen Ladungen, welche auf Textilgarnen während der Bearbeitung auf Textilmaschinen entstehen, verringert werden.contain. Herein, R is an organic radical, X is an oxygen or sulfur atom or an imino group, and m is zero or one. Such compositions are intended to reduce the electrical charges which arise on textile yarns during processing on textile machines.
Die vorliegende Erfindung betrifft emulgierbare Schmälzmittel, welche neben einem überwiegenden Anteil eines mineralischen Schmieröls noch als an sich bekannte Emulgatoren ein öllösliches Naphthasulfonat, einen öUöslichen nichtionischen Emulgator und einen stickstoffhaltigen Emulgator enthalten, der in Öl löslich, aber in Wasser praktisch unlöslich ist.The present invention relates to emulsifiable lubricants, which in addition to a predominant Part of a mineral lubricating oil still known as emulsifiers, an oil-soluble naphthasulfonate, contain an soluble nonionic emulsifier and a nitrogenous emulsifier which soluble in oil but practically insoluble in water.
Um die Emulgierung der Schmälze in Wasser zu erleichtern, enthalten die Zusammensetzungen gemäß der Erfindung noch bis zu 10% Wasser. Vorzugsweise verwendet man wäßrige 2°/oige Emulsionen des Gemisches. Die Emulgierung tritt beim Verdünnen mit Wasser rasch ein, und die wäßrigen Emulsionen haben eine hohe Beständigkeit.In order to facilitate the emulsification of the sludge in water, the compositions contain according to of the invention still up to 10% water. Aqueous 2% emulsions are preferably used Mixture. Emulsification occurs rapidly on dilution with water, and so does the aqueous emulsions have a high resistance.
Das erfindungsgemäß verwendete mineralische Schmieröl kann ein schwach raffiniertes Öl sein, welches durch Destillation, Lösungsmittelextraktion, Behandlung mit Ton oder verdünnten Säuren od. dgl. raffiniert ist, oder ein hoch raffiniertes Öl, welches mit rauchender Schwefelsäure mit oder ohne vorausgehende Lösungsmittelbehandlung erhalten ist. Die Öle können hochparaffinische Öle sein, die mindestens 65 Gewichtsprozent Anteile enthalten, die bei der Behandlung mit konzentrierter Schwefelsäure unsulfoniert bleiben, oder sie können naphthenische und aromatische Bestandteile enthalten. Zur Verwendung in Textilölzusammensetzungen werden hoch raffinierte Anmelder: »Shell« Research Limited, LondonThe mineral lubricating oil used in the invention can be a weakly refined oil, which od by distillation, solvent extraction, treatment with clay or dilute acids. Like. refined, or a highly refined oil which is preceded with fuming sulfuric acid with or without Solvent treatment is obtained. The oils can be highly paraffinic oils, at least Contain 65 percent by weight that unsulfonated when treated with concentrated sulfuric acid remain, or they can contain naphthenic and aromatic components. For use in textile oil compositions there are highly refined applicants: "Shell" Research Limited, London
Vertreter: Dr. K. Schwarzhans, Patentanwalt, München 19, Romanplatz 10Representative: Dr. K. Schwarzhans, patent attorney, Munich 19, Romanplatz 10
Beanspruchte Priorität: Großbritannien vom 29. März 1954 (Nr. 9079)Claimed priority: Great Britain, March 29, 1954 (No. 9079)
Maurice Elton, Sidcup, Kent,Maurice Elton, Sidcup, Kent,
und Philip Alan Winsor,and Philip Alan Winsor,
Willington, Kelsall, Cheshire (Großbritannien),Willington, Kelsall, Cheshire (UK),
sind als Erfinder genannt wordenhave been named as inventors
Öle wegen ihrer größeren Beständigkeit und ihrem Widerstandsvermögen gegen Geruch- und Farbbildung
bei der Einwirkung von Licht und Luft vorgezogen. Sie sollen einen genügend hohen Flammpunkt aufweisen.
Die in den erfindungsgemäßen Zusammensetzungen verwendeten öUöslichen Naphthasulfonate werden als
Nebenprodukte bei der Herstellung von technischem Weißöl und Transformatorenöl erhalten. Die Behandlung
solcher Öle mit Oleum führt zur Bildung einer unteren sauren Schlammschicht und einer oberen
Ölschicht, welche öllösliche Naphthasulfonsäuren bzw. sogenannte»Mahagony-Säuren«enthält.DieseNaphthasulfonsäuren
werden isoliert durch Behandlung der Ölschicht mit einer Lösung von Alkalihydroxyd bzw.
Ammoniak oder einem aliphatischen Amin oder Alkylolamin, wie Triäthanolamin; die so erhaltenen
rohen Salze können gereinigt werden. Die Naphthasulfonsäuren, deren Salze in den Zusammensetzungen
gemäß der Erfindung verwendet werden, haben ein durchschnittliches Molgewicht von 420 bis 450. Der
Anteil an Naphthasulfonat in der Schmälze beträgt 2 bis 20 Gewichtsprozent.Oils are preferred because of their greater resistance and their resistance to odor and color formation when exposed to light and air. They should have a sufficiently high flash point.
The oil-soluble naphthasulfonates used in the compositions according to the invention are obtained as by-products in the production of technical white oil and transformer oil. The treatment of such oils with oleum leads to the formation of a lower acidic sludge layer and an upper oil layer which contains oil-soluble naphthasulphonic acids or so-called "mahogany acids." These naphthasulphonic acids are isolated by treating the oil layer with a solution of alkali hydroxide or ammonia or an aliphatic amine or alkylolamine, such as triethanolamine; the crude salts thus obtained can be purified. The naphthasulfonic acids, the salts of which are used in the compositions according to the invention, have an average molecular weight of 420 to 450. The proportion of naphthasulfonate in the sludge is 2 to 20 percent by weight.
Als öllösliche nichtionische Emulgatoren werden z. B. verwendet:As oil-soluble nonionic emulsifiers, for. B. used:
1. Öllösliche einwertige Alkohole, z. B. die Octanole, Nonanole, Decanole, Undecanole, Dodecanole und andere höhere aliphatische Alkohole, z. B. auch nach dem OXO-Verfahren hergestellte Alkohole, oder1. Oil-soluble monohydric alcohols, e.g. B. the octanols, Nonanols, decanols, undecanols, dodecanols and other higher aliphatic alcohols, e.g. Belly alcohols produced by the OXO process, or
209 579/270209 579/270
3 43 4
Fettalkohole ζ. B. aus Spermöl. Auch öllösliche aro- Gemische dieser stickstoffhaltigen Emulgatoren be-Fatty alcohols ζ. B. from sperm oil. Oil-soluble aroma mixtures of these nitrogen-containing emulsifiers are also
matische und cycloaliphatische Alkohole, wie Benzyl- nutzen.matic and cycloaliphatic alcohols, such as benzyl use.
alkohol und Methylcyclohexanol, sind geeignet. Naphthasulfonate, wie Natriumnaphthasulfonat, be-alcohol and methylcyclohexanol are suitable. Naphthasulfonates, such as sodium naphthasulfonate,
2. Öllösliche zweibasische Alkohole, wie Hexylen- günstigen die Bildung von Emulsionen von sehr glykole, Octylenglykole, Decylenglykole und höhere 5 geringer Teilchengröße, welche infolgedessen durch-Glykole. _ scheinend oder klar sind. Einfache Emulsionen von2. Oil-soluble dibasic alcohols, such as hexylene- favorable the formation of emulsions of very glycols, octylene glycols, decylene glycols and higher 5 smaller particle sizes, which are consequently due to glycols. Shining or clear. Simple emulsions of
3. Öllösliche substituierte Alkohole z. B. mit Äther- Wasser, Öl und Naphthasulfonat haben jedoch einen und bzw. oder Estergruppen. Geeignet sind die Teil- unerwünscht hohen Reibungskoeffizienten, wenn sie ester mehrwertiger Alkohole und Fettsäuren, wie als Textilfaserschmiermittel verwendet werden; ins-Glycerinmono- oder -dioleat oder -stearat, Äthylen- io besondere bei der Anwendung auf Polyamidfasern, glykolmonooleat oder -stearat, und die Monoester Der Zusatz von stickstoffhaltigen Emulgatoren oder -äther von Polyäthylenglykolen, wie die Mono- begünstigt die Beständigkeit der Emulsion und ergibt oleate oder -stearate von Monoäthylenglykol. Zusammensetzungen, welche die Reibung zwischen3. Oil-soluble substituted alcohols e.g. B. with ether, water, oil and naphthasulfonate, however, have one and / or ester groups. The partially undesirably high coefficients of friction are suitable if they polyhydric alcohol and fatty acid esters such as are used as textile fiber lubricants; ins-glycerine mono- or dioleate or stearate, ethylene io especially when used on polyamide fibers, glycol monooleate or stearate, and the monoesters The addition of nitrogen-containing emulsifiers or ethers of polyethylene glycols, such as the mono- favors the stability of the emulsion and results oleates or stearates of monoethylene glycol. Compositions that reduce the friction between
Verbindungen, wie Glyceryldioleat, haben die wert- den Fasern erniedrigen. Wenn die stickstoffhaltigenCompounds such as glyceryl dioleate have degrade the valuable fibers. If the nitrogenous
volle Eigenschaft einer Erniedrigung der Friktions- 15 Emulgatoröle jedoch in zu hoher Konzentration imfull property of lowering the friction emulsifier oils, but in too high a concentration in the
werte der Zusammensetzungen. Verhältnis zu der Menge des Naphthasulfonates invalues of the compositions. Relation to the amount of naphthasulfonate in
Man kann einen einzigen öllöslichen nichtionischen dem Gemisch vorhanden sind, wird der dynamische Emulgator verwenden; oft ist es zweckmäßig, ein Reibungskoeffizient größer als der statische Reibungs-Gemisch von zwei oder mehr Verbindungen zu be- koeffizient, wodurch sich Schwierigkeiten bei der nutzen, um die beste Auswaschbarkeit und eine 20 Behandlung der geölten Fasern ergeben. Bei Textilrasche Emulsionsbildung zu erzielen. So haben sich faserschmiermitteln soll die Menge des stickstoffein Gemisch von Glyceryldioleat und einer unter- haltigen Emulgators gerade ausreichend sein, um eine geordneten Menge von Diglykollaureat und ein Zusammensetzung mit geeigneten Friktionseigenschaf-Gemisch von Glyceryldioleat mit untergeordneten ten, d. h. mit einem statischen Reibungskoeffizienten, Mengen von Diglykollaureat und Monoäthylenglykol- 25 der größer ist als der dynamische Reibungskoeffizient, monooleat als besonders wirksam erwiesen. Der zu erzeugen.One can have a single oil-soluble nonionic mixture that becomes dynamic Use emulsifier; It is often useful to have a coefficient of friction greater than the static friction mixture of two or more connections too coefficient, which leads to difficulties in the use to give the best washability and a 20 treatment of the oiled fibers. At Textilrasche To achieve emulsification. So have fiber lubricants supposed to be the amount of nitrogen Mixture of glyceryl dioleate and an entertaining emulsifier will be just sufficient to produce a ordered amount of diglycol laureate and a composition with suitable frictional properties mixture of glyceryl dioleate with subordinate ten, d. H. with a static coefficient of friction, Amounts of diglycol laureate and monoethylene glycol which is greater than the dynamic coefficient of friction, monooleate proved to be particularly effective. The generate.
nichtionische Emulgator beträgt zweckmäßig 0,5 bis Zusätzlich zu den vorgenannten wesentlichennonionic emulsifier is expediently 0.5 to in addition to the abovementioned essential ones
10 Gewichtsprozent der Gesamtzusammensetzung. Bestandteilen können auch andere Stoffe, welche10 percent by weight of the total composition. Components can also contain other substances, which
Der in den erfindungsgemäßen Gemischen ver- spezielle Eigenschaften aufweisen, in geringen MengenWhich have special properties in the mixtures according to the invention, in small amounts
wendete stickstoffhaltige Emulgator ist in Mineralöl 30 den Gemischen gemäß der Erfindung einverleibtThe nitrogenous emulsifier used is incorporated in mineral oil 30 in the mixtures according to the invention
löslich, aber in Wasser im wesentlichen unlöslich. werden, wie z. B. Lösungsmittel, die rasche Emulsions-soluble but essentially insoluble in water. become, such as B. Solvents, the rapid emulsion
Geeignete stickstoffhaltige Emulgatoren dieser Art bildung begünstigen und die Stabilität der EmulsionSuitable nitrogen-containing emulsifiers of this type promote formation and the stability of the emulsion
sind die primären, sekundären und tertiären Amine, verbessern. Solche Stoffe sind z. B. ferner einwertigeare the primary, secondary and tertiary amines, improve. Such substances are z. B. also monovalent
welche mindestens eine hydrophobe Gruppe in Bin- Alkohole mit weniger als 8 Kohlenstoffatomen imwhich has at least one hydrophobic group in bin alcohols with fewer than 8 carbon atoms in the
dung an das Stickstoffatom enthalten, wie z. B. 35 Molekül, wie Isopropylalkohol, Butyl- und Amyl-application to the nitrogen atom, such as. B. 35 molecule, such as isopropyl alcohol, butyl and amyl
Dodecylamin, Octadecylamin, Dicetylamin, N-Octa- alkohol, Cyclohexanol, Diacetonalkohol, Phenole, dieDodecylamine, octadecylamine, dicetylamine, N-octa alcohol, cyclohexanol, diacetone alcohol, phenols, the
decyl-N-oxyäthylamin, N-Alkyl-N-oxypropylpiper- Glykole wie Hexylenglykql, Polyäthylenglykol unddecyl-N-oxyäthylamine, N-alkyl-N-oxypropylpiper glycols such as hexylene glycol, polyethylene glycol and
idine, in welchen die Alkylreste von Kokosnußöl ab- Glykolmonoäther, wie der Äthyl- oder Butyläther vonidine, in which the alkyl radicals of coconut oil from glycol monoether, such as the ethyl or butyl ether from
geleitet sind, und die Monoacyl- oder as-Diacylderi- Äthylenglykol.are directed, and the monoacyl or as-diacylderi ethylene glycol.
vate von aliphytischen Polyaminen, wie Oleyläthylen- 40 Gewünschtenfalls können anionische Emulgatoren diamin und as-Distearyläthylendiamin. Besonders ge- in geringeren Mengen den erfindungsgemäßen Geeignete stickstoffhaltige Emulgatoren zur Anwendung mischen zusätzlich einverleibt werden, wie z. B. die in den Zusammensetzungen gemäß vorliegender Er- Alkaliseifen höherer Fett- oder Harzsäuren, Alkalifindung sind die organischen Verbindungen, welche salze von Schwefelsäureestern höherer primärer und keine Sulfonsäuregruppen enthalten, aber die Atom- 45 sekundärer Alkohole und Alkalisalze von Alkylarylgruppierung sulfonaten. Diese unterstützen die rasche Emulsions-vate of aliphytic polyamines, such as oleylethylene 40, if desired, anionic emulsifiers diamine and as-distearylethylenediamine. Particularly those suitable according to the invention are used in smaller amounts Mixing nitrogen-containing emulsifiers for use can also be incorporated, such as. B. the in the compositions according to the present invention, alkali soaps of higher fatty or resin acids, alkali finding are the organic compounds, which are salts of sulfuric acid esters of higher primary and do not contain sulfonic acid groups, but contain the atomic 45 secondary alcohols and alkali salts of alkylaryl groups sulfonates. These support the rapid emulsion
^N — bildung beim Verdünnen mit Wasser.^ N - formation when diluted with water.
j^y- Q Antioxydationsmittel sind ebenfalls als Zusatzstoffej ^ y- Q antioxidants are also available as additives
m \ / für die erfindungsgemäßen Gemische geeignet, z. B. m \ / suitable for the mixtures according to the invention, e.g. B.
N χ 50 2,4-Dimethyl-6-tert.-butylphenol, N-Butyl-p-phenylen-N χ 50 2,4-dimethyl-6-tert.-butylphenol, N-butyl-p-phenylene-
aufweisen. diamin, Tetramethyldiammodiphenylmethan.exhibit. diamine, tetramethyldiammodiphenylmethane.
Hierin ist R ein Kohlenwasserstoffradikal, X ein Auch Schaumverhinderungsmittel, wie Silikone und Sauerstoff- oder Schwefelatom oder eine Iminogruppe, Dispersionen von Ν,Ν'-Distearyläthylendiamin oder und m ist Null oder Eins. Der Rest R enthält Vorzugs- Ν,Ν'-Distearylhexamethylendiamin, können dem Geweise mindestens 8 Kohlenstoffatome. 55 misch einverleibt werden.Here, R is a hydrocarbon radical, X is also an anti-foaming agent, such as silicone and oxygen or sulfur atom or an imino group, dispersions of Ν, Ν'-distearylethylenediamine or and m is zero or one. The radical R contains preferred Ν, Ν'-distearylhexamethylenediamine, may contain at least 8 carbon atoms. 55 can be incorporated.
Typische Verbindungen, welche diese Struktur auf- Salicylanilid ist ein als Zusatz geeignetes Fungizid,Typical compounds that have this structure - salicylanilide is a fungicide suitable as an additive,
weisen, sind die entsprechend substituierten Iso- Ferner können auch Korrosionsverhinderer einverleibtThe appropriately substituted ISOs are also used. Corrosion inhibitors can also be incorporated
harnstoffe, Isothioharnstoffe, Guanidine, Iminazole, werden.ureas, isothioureas, guanidines, iminazoles.
Imidazoline und Pyrimidine. Beispiele solcher Ver- Die emulgierbaren Gemische gemäß der ErfindungImidazolines and pyrimidines. Examples of such emulsifiable mixtures according to the invention
bindungen sind O-Äthylharnstoff, S-Dodecylthioharn- 60 werden vorzugsweise so eingestellt, daß eine 2%igebonds are O-ethylurea, S-dodecylthiourea are preferably adjusted so that a 2%
stoff, 1-Guanidinpalmitinsäure, 1-Oxyäthylguanidin, Emulsion in Wasser einen pH-Wert größer als 7, vor-substance, 1-guanidine palmitic acid, 1-oxyethylguanidine, emulsion in water with a pH value greater than 7,
2-Undecylimidazolin, l-jö-Oxyäthyl-2-heptadecylen- zugsweise größer als 9, aufweist,2-Undecylimidazoline, l-jö-Oxyäthyl-2-heptadecylen- preferably greater than 9, has,
imidazolin, 2-Naphthenylimidazolin, 2-Heptadecyl- Die erfindungsgemäßen Zusammensetzungen wer-imidazoline, 2-naphthenylimidazoline, 2-heptadecyl- The compositions according to the invention are
benziminazol, 2-Undecylpyrimidin und 1-Benzyl- den auf die Textilfasern nach bekannten Verfahrenbenziminazol, 2-undecylpyrimidine and 1-benzylden on the textile fibers according to known methods
2-heptadecylbenziminazol. Es können auch Salze 65 aufgebracht, z. B. durch Besprühen der laufenden2-heptadecylbenziminazole. Salts 65 can also be applied, e.g. B. by spraying the current
dieser Verbindungen mit anorganischen oder orga- Textilgarne oder durch Hindurchführen der Textil-these compounds with inorganic or organic textile yarns or by passing through the textile
nischen Säuren, wie Salzsäure, Essigsäure, Stearinsäure fäden durch Bäder oder über Dochte oder andere,niche acids such as hydrochloric acid, acetic acid, stearic acid threads through baths or via wicks or others,
oder Ölsäure, verwendet werden. Man kann auch ähnliche Vorrichtungen.or oleic acid can be used. Similar devices can also be used.
Die Beispiele erläutern Textilöle gemäß der Erfindung, wobei die erwähnten Teile Gewichtsteile sind.The examples illustrate textile oils according to the invention, the parts mentioned being parts by weight.
Es wird ein Gemisch hergestellt aus 63 Teilen Spindelöl, 4,9 Teilen von l-jS-Oxyäthyl-2-heptadecylenimidazolin, 4,9 Teilen Glycerindioleat, 1,2 Teilen Diglykollaureat, 9,8 Teilen öllöslicher Natriumnaphthasulfonate (Molgewicht 420 bis 450), 6,5 Teilen Kolophonium, 3,3 Teilen Ölsäure, 1,2 Teilen Kaliumhydroxyd, 2,6 Teilen Isopropylalkohol und 2,6 Teilen Wasser.A mixture is prepared from 63 parts of spindle oil, 4.9 parts of l-jS-oxyethyl-2-heptadecylenimidazoline, 4.9 parts of glycerol dioleate, 1.2 parts of diglycol laurate, 9.8 parts of oil-soluble sodium naphthasulfonate (Molar weight 420 to 450), 6.5 parts of rosin, 3.3 parts of oleic acid, 1.2 parts Potassium hydroxide, 2.6 parts isopropyl alcohol and 2.6 parts water.
Dieses Gemisch stellt ein gutes Behandlungsöl für Viskosekunstseide dar, wenn es in wäßriger Emulsion von 2 Volumprozent verwendet wird.This mixture makes a good treatment oil for viscose rayon when it is in an aqueous emulsion of 2 percent by volume is used.
Man stellt ein Gemisch her aus 54,6 Teilen Spindelöl, 4,8 Teilen l-^-Oxyäthyl-2-heptadecylenimidazolin, 4,8 Teilen Glycerindioleat, 0,6 Teilen Diglykollaureat, 13,0 Teilen öllöslicher Natriumnaphthasulfonate (Molgewicht 420 bis 450), 8,7 Teilen Kolophonium,A mixture is made of 54.6 parts of spindle oil, 4.8 parts of l - ^ - oxyethyl-2-heptadecylenimidazoline, 4.8 parts of glycerol dioleate, 0.6 parts of diglycol laurate, 13.0 parts of oil-soluble sodium naphthasulfonate (Molecular weight 420 to 450), 8.7 parts of rosin,
4.4 Teilen Ölsäure, 2,1 Teilen Kaliumhydroxyd,4.4 parts of oleic acid, 2.1 parts of potassium hydroxide,
3.5 Teilen Isopropylalkohol und 3,5 Teilen Wasser. Diese Mischung ist leicht mit Wasser zu emulgieren3.5 parts isopropyl alcohol and 3.5 parts water. This mixture is easy to emulsify with water
unter Bildung einer klaren 10%igen Öl-in-Wasser-Emulsion, welche noch nach 2wöchiger Lagerung unverändert ist.forming a clear 10% oil-in-water emulsion, which is still unchanged after 2 weeks of storage.
Eine 2 volumprozentige Emulsion in destilliertem Wasser hat einen pH-Wert von 10,9. Wenn die wäßrige Emulsion zur Schmierung von Polyamidfäden verwendet wird, beträgt der statische Reibungskoeffizient 0,185 und der dynamische Reibungskoeffizient 0,175A 2 percent by volume emulsion in distilled water has a pH of 10.9. When the watery Emulsion is used to lubricate polyamide threads, the static coefficient of friction is 0.185 and the dynamic coefficient of friction 0.175
3535
Claims (9)
Britische Patentschriften Nr. 690 895, 703 499;
belgische Patentschrift Nr. 445 755.Considered publications:
British Patent Nos. 690 895, 703 499;
Belgian patent specification No. 445 755.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9079/54A GB753749A (en) | 1954-03-29 | 1954-03-29 | Improvements in or relating to textile oils |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1129255B true DE1129255B (en) | 1962-05-10 |
Family
ID=9864957
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DES43220A Pending DE1129255B (en) | 1954-03-29 | 1955-03-28 | Emulsifiable textile oil |
Country Status (6)
Country | Link |
---|---|
US (1) | US2853453A (en) |
BE (1) | BE536867A (en) |
DE (1) | DE1129255B (en) |
FR (1) | FR1127014A (en) |
GB (1) | GB753749A (en) |
NL (2) | NL103782C (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3056705A (en) * | 1958-06-19 | 1962-10-02 | Owens Corning Fiberglass Corp | Surface treated glass and similar fibers |
BE591186A (en) * | 1959-05-25 | 1900-01-01 | ||
US3522175A (en) * | 1965-02-13 | 1970-07-28 | Kao Corp | Lubricant composition for synthetic fibers |
US3485913A (en) * | 1965-10-20 | 1969-12-23 | Toho Beslon Co | New method of manufacturing acrylic fibers and the related products |
US3850819A (en) * | 1972-08-25 | 1974-11-26 | Ici America Inc | Low fuming spin finish for nylon weaving yarns |
ES426477A1 (en) * | 1973-05-26 | 1976-07-01 | Hoechst Ag | Fiber-lubricating compositions |
US4082679A (en) * | 1977-03-10 | 1978-04-04 | Witco Chemical Corporation | Light stabilized textile mineral oil |
US4186126A (en) * | 1978-04-11 | 1980-01-29 | Messick John J | Sulfonate antioxidants for synthetic and natural rubber |
GB2285630A (en) * | 1994-01-12 | 1995-07-19 | Diversey Corp | Aqueous lubricant compositions for conveyor tracks |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE445755A (en) * | 1941-06-07 | |||
GB690895A (en) * | 1950-02-18 | 1953-04-29 | Celanese Corp | Yarn lubricants |
GB703499A (en) * | 1951-05-17 | 1954-02-03 | Shell Refining & Marketing Co | Improvements in and relating to the processing of textile yarns, threads, filaments and the like |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2036470A (en) * | 1931-10-24 | 1936-04-07 | Standard Oil Co California | Emulsifiable oil product and process of making the same |
US2025434A (en) * | 1933-07-01 | 1935-12-24 | American Enka Corp | Lubricating natural and artificial fibers |
US2122593A (en) * | 1935-03-05 | 1938-07-05 | Henry A Stafford | Treatment of textile fibers |
-
0
- NL NL195998D patent/NL195998A/xx unknown
-
1954
- 1954-03-29 GB GB9079/54A patent/GB753749A/en not_active Expired
-
1955
- 1955-03-14 US US494256A patent/US2853453A/en not_active Expired - Lifetime
- 1955-03-28 FR FR1127014D patent/FR1127014A/en not_active Expired
- 1955-03-28 BE BE536867A patent/BE536867A/nl unknown
- 1955-03-28 NL NL195998A patent/NL103782C/nl active
- 1955-03-28 DE DES43220A patent/DE1129255B/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE445755A (en) * | 1941-06-07 | |||
GB690895A (en) * | 1950-02-18 | 1953-04-29 | Celanese Corp | Yarn lubricants |
GB703499A (en) * | 1951-05-17 | 1954-02-03 | Shell Refining & Marketing Co | Improvements in and relating to the processing of textile yarns, threads, filaments and the like |
Also Published As
Publication number | Publication date |
---|---|
FR1127014A (en) | 1956-12-06 |
NL103782C (en) | 1962-09-17 |
NL195998A (en) | 1900-01-01 |
GB753749A (en) | 1956-08-01 |
US2853453A (en) | 1958-09-23 |
BE536867A (en) | 1955-09-28 |
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