EP0022239A1 - Agent and process for wet paraffinic treatment of yarns - Google Patents
Agent and process for wet paraffinic treatment of yarns Download PDFInfo
- Publication number
- EP0022239A1 EP0022239A1 EP80103725A EP80103725A EP0022239A1 EP 0022239 A1 EP0022239 A1 EP 0022239A1 EP 80103725 A EP80103725 A EP 80103725A EP 80103725 A EP80103725 A EP 80103725A EP 0022239 A1 EP0022239 A1 EP 0022239A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- alkyl
- oder
- alkenyl
- paraffin
- hydrogen
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims description 9
- 239000012188 paraffin wax Substances 0.000 claims abstract description 32
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 22
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 14
- 239000001257 hydrogen Substances 0.000 claims abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 7
- 150000001412 amines Chemical class 0.000 claims abstract description 6
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 6
- 238000004018 waxing Methods 0.000 claims abstract description 6
- 229920000151 polyglycol Polymers 0.000 claims abstract description 5
- 239000010695 polyglycol Substances 0.000 claims abstract description 5
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 4
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 3
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 3
- 150000002170 ethers Chemical class 0.000 claims abstract description 3
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 3
- 150000002367 halogens Chemical group 0.000 claims abstract description 3
- 238000002844 melting Methods 0.000 claims abstract description 3
- 230000008018 melting Effects 0.000 claims abstract description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims abstract description 3
- 239000010452 phosphate Substances 0.000 claims abstract description 3
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 3
- 239000000203 mixture Substances 0.000 claims description 12
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 claims description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract description 4
- 125000002252 acyl group Chemical group 0.000 abstract description 4
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 abstract description 2
- 125000005843 halogen group Chemical group 0.000 abstract description 2
- 239000007788 liquid Substances 0.000 abstract 1
- 239000001993 wax Substances 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 description 18
- 238000004043 dyeing Methods 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 4
- 235000013162 Cocos nucifera Nutrition 0.000 description 3
- 244000060011 Cocos nucifera Species 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 238000009940 knitting Methods 0.000 description 2
- 229940055577 oleyl alcohol Drugs 0.000 description 2
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- CWEGOSBBFLRMKN-YPKPFQOOSA-N (z)-n,n-diethyloctadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN(CC)CC CWEGOSBBFLRMKN-YPKPFQOOSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- -1 Fatty acid esters Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000002752 cationic softener Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- 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
- D06M13/46—Compounds containing quaternary nitrogen atoms
- D06M13/47—Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds
- D06M13/473—Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds having five-membered heterocyclic rings
-
- 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
- D06M13/10—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 oxygen
- D06M13/165—Ethers
-
- 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
- D06M13/388—Amine oxides
-
- 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
-
- 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
Definitions
- the paraffin dispersion is produced by intensive mixing of all components at temperatures of above 70-80 ° C., a particular advantage being that no homogenizer is required.
- the clear dispersions are stable and can be diluted with cold water to the desired final concentration in an aqueous liquor.
- These paraffin dispersions which form fine dispersions that are stable in storage and shear when diluted with water, can be used instead of solid dry paraffin for the paraffin waxing of staple fiber yarns from native and synthetic fibers. They can be called pseudo-cationically dispersed systems and are characterized by high substantivity when used in a long fleet.
- the pH of the paraffin dispersions is advantageously 3 - 6 and is adjusted to this value with acids.
- the paraffin dispersions are applied in customary dyeing machines such as those used for dyeing textile yarns.
- the process is carried out in liquor ratios of 1: 5 to 1:40 at temperatures of 10 - 90 ° C.
- the application is advantageously carried out after the dyeing process, by rinsing the yarn with a dispersion of the type described above in a dilute aqueous form delt, which contains 0.1-2% by weight, preferably 0.3-1% by weight, of the composition of the composition described above, based on the weight of the yarn.
- the yarns paraffinized in this way have a pleasantly soft feel, which makes the application of an additional plasticizer unnecessary. Due to the dispersing agents built into the systems, there is no electrostatic charge interfering with knitting.
- the paraffin dispersions according to the invention also do not contain any organic solvents which could be harmful to the environment, especially when working in open apparatus. They only contain the inexpensive paraffin as a sliding component and do not require any additional components for conveying smoothness and the softening effect, e.g. Fatty acid esters, which are expensive compared to paraffin.
- the paraffin dispersions according to the invention have a high substantivity, combined with a high wetting power, which enables application even in short test times and at a low temperature.
- the dispersions according to the invention give yarns a high antistatic effect combined with high smoothness.
- dispersions described in the following examples are prepared by simply mixing the individual components. Percentages are to be understood as percentages by weight. EO means ethylene oxide.
- Paraffin dispersion consisting of 15 parts of paraffin (mp. 50-53 ° C.), 5 parts of an imidazoline of the formula I, where R is a mixture of 45% C 15 and 55% C 17 alkyl, R is a mixture of 45% C16 and 55 % C 18 acyl, R 2 is hydrogen, n 2 X CH 3 CO 2 , 4 parts of cocoalkyldimethylamine oxide, 10 parts of coconut fatty alcohol x 5 EO, 100 parts of deionized water. pH value: approx. 4
- Paraffin dispersion consisting of 17 parts of paraffin (mp. 50-53 ° C.), 7 parts of the imidazoline according to Example 1, 4 parts of oleyl diethylamine oxide, 8 parts of oleyl alcohol x 7 EO, 100 parts of deionized water. pH: approx.4.2
- Paraffin dispersion consisting of 13 parts paraffin (mp 52-54 ° C), 6 parts of an imidazoline of the formula I, where R is a mixture of 5% C 13 , 30% C 15 '35% C 17 alkyl and 30% C 17 -Alkenyl, R 1 is a mixture of 5% C 14 , 30% C 16 , 35% C 18 -acyl and 30% C 1 $ -acenyl, R 2 is hydrogen, n 2 and X acetate, 3 parts of an amine oxide of the formula II, where R is a mixture of 70% C12 and 30% C 14 alkyl, R 1 and R 2 is methyl and n 0 and 6 parts of coconut fatty alcohol x 6 EO 6 parts oleyl alcohol x 5 EO 100 parts of demineralized water. pH: 4.5
- Paraffin dispersion consisting of 14 parts of paraffin (mp. 52-54 ° C.), 2.4 parts of the imidazoline used in Example 1, 0.6 part of an imidazoline of the formula I, where R is a mixture of 5% C 13-30 % C. 15 '35% C 17 alkyl and 30% C 17 alkenyl, R 1 and R 2 hydrogen, n 2 and X CH 3 COO - means 6 parts cocoalkyldimethylamine oxide and 10 parts C 12 / C 14 alcohol x 10 EO, 100 parts of demineralized water. pH: 4.1
- Yarns made from 100% PES were treated in a cross-wound dyeing machine under HT conditions after previous dispersion dyeing and rinsing at 40 ° C. for 30 minutes in a liquor ratio 1:10 at pH 5.5 with the dispersions described in Examples 1-4 in dilute form . These dispersions were diluted to such an extent that the concentration of components a) to d) in the liquor, based on the weight of the yarn, was 2% by weight. After drying, the PES material had a smooth, soft feel, which can only be achieved for dry-waxed yarns with the addition of a cationic softener.
- the wet waxed yarns are very smooth.
- the coefficient of friction, measured in the measuring arrangement described in DE-OS 24 16 430, gave the following values at the measuring speeds 20 and 100 m / minute: The material was easy to process and showed a uniform, homogeneous surface after being knitted.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
\Mittel zum Flüssigparaffinieren von Garnen bestehend aus
- a) 5 - 20 % Paraffin, Schmelzbereich 45 - 60°C,
- b) 2-10%einesodermehrererAlkylimidazolinederFormell
- wobei R C12-C22-Alkyl, Alkenyl oder Hydroxialkyl,
- R1 Wasserstoff oder C1-C22-gesättigtes oder ungesättigtes aliphatisches oder aromatisches Acyl,
- R2 Wasserstoff, Cl-C4-Alkyl oder Hydroxialkyl,
- n Zahlen von 2 bis 6, und
- X ein Halogen-, C1-C4-Alkylsulfat-, C1-C4-Dialkylphosphat- oder ein C1-C4-Alkyl- carboxylat-anion bedeuten;
- c) 1 - 5 % eines oder mehrerer Aminoxide der allgemeinen Formel II
- wobei R C8-C12-Alkyl- oder Alkenyl,
- R, C1-C4-Alkyl,
- R2 Wasserstoff oder Cl-C4-Alkyl und
- n Zahlen von Null bis 6 bedeuten;
- d) 5-20%einesodermehrererPolyglykoläthsrderFormel III
wobei R Ca-C, s-Alkyl- oder Alkenyl und n Zahlen von 3 bis 12 bedeuten; und der an 100 Gew.-% fehlende Rest ist Wasser.
- a) 5 - 20% paraffin, melting range 45 - 60 ° C,
- b) 2-10% of one or more alkylimidazolines of the formal
- where RC 12 -C 22 alkyl, alkenyl or hydroxyalkyl,
- R 1 is hydrogen or C 1 -C 22 -saturated or unsaturated aliphatic or aromatic acyl,
- R 2 is hydrogen, C 1 -C 4 alkyl or hydroxyalkyl,
- n numbers from 2 to 6, and
- X is a halogen, C 1 -C 4 alkyl sulfate, C 1 -C 4 dialkyl phosphate or a C 1 -C 4 alkyl carboxylate anion;
- c) 1-5% of one or more amine oxides of the general formula II
- where RC 8 -C 12 alkyl or alkenyl,
- R, C 1 -C 4 alkyl,
- R 2 is hydrogen or C 1 -C 4 alkyl and
- n is a number from zero to 6;
- d) 5-20% of one or more polyglycol ethers of Formula III
where RC a -C, s alkyl or alkenyl and n are numbers from 3 to 12; and the remainder missing in 100% by weight is water.
Description
Um gefärbte oder ungefärbte Stapelfasergarne für das Stricken einsetzen zu können, ist es üblich, diese während eines Umspulprozesses mit einem festen Paraffinblock zu behandeln. Dabei wird auf die Faser eine bestimmte Menge festen Paraffins aufgebracht und erhält den für den Weiterverarbeitungsprozess nötigen niedrigen Reibungskoeffizienten, d.h. eine hohe Glätte. Es ist verständlich, dass dieser Vorgang des sogenannten Trockenparaffinierens in der Praxis nicht unproblematisch ist. Je nach Druck zwischen Faser und Paraffinblock kann die Auflage an Trockenparaffin schwanken. Das feste Paraffin kann in nachfolgenden Erhitzungsprozessen (Bügeln, Fixieren) wegsublimieren und damit zum Ausblühen neigen. Das starre Trockenparaffin verleiht dem Material zwar eine ausreichende Glätte für die Weiterverarbeitung, ein eigentlicher Weichmachungseffekt ist mit seiner Applikation jedoch nicht verbunden. Damit besteht für trockenparaffinierte Artikel die Notwendigkeit, in einer nachträglichen Arbeitsstufe diese Artikel durch Aufbringen eines zusätzlichen Weichmachers noch weichzumachcn.In order to be able to use dyed or undyed staple fiber yarns for knitting, it is common to treat them with a solid paraffin block during a rewinding process. A certain amount of solid paraffin is applied to the fiber and receives the low coefficient of friction required for the further processing process, i.e. a high smoothness. It is understandable that this process of so-called dry waxing is not without problems in practice. Depending on the pressure between the fiber and the paraffin block, the amount of dry paraffin may fluctuate. The solid paraffin can sublime away in subsequent heating processes (ironing, fixing) and thus tend to bloom. The rigid dry paraffin gives the material sufficient smoothness for further processing, but there is no actual softening effect associated with its application. Thus there is a need for dry-waxed articles to soften these articles in a subsequent work step by applying an additional plasticizer.
Es stellt sich somit die Aufgabe, Stapelfasergarnen eine für die Weiterverarbeitung nötige gleichmässige niedrige Reibung, d.h. hohe Glätte in.Verbindung mit zufriedenstellender Weichheit zu geben. Die Aufgabe wird dadurch gelöst, dass ein Mittel zur Flüssigparaffinierung von Garnen folgender Zusammensetzung eingesetzt wird:
- a) 5 - 20 % Paraffin, Schmelzbereich 45 - 60° C
- b) 2 - 10 % eines oder mehrerer Alkylimidazoline der Formel I
- wobei R C12-C22-Alkyl, Alkenyl oder Hydroxialkyl,
- R1 Wasserstoff oder C1-C22-gesättigtes oder ungesättigtes aliphatisches oder aromatisches Acyl,
- R2 Wasserstoff, C1-C4-Alkyl oder Hydroxialkyl, n Zahlen von 2 - 6 und
- X ein Halogen-, C1-C4-Alkylsulfat-, C1-C4-Di- alkylphosphat- oder ein C1-C4-Alkylcarboxylat- anion bedeuten.
- c) 1 - 5 % eines oder mehrerer Aminoxide der allgemeinen Formel II
- wobei R C8-C12-Alkyl oder Alkenyl,
- R1 C1-C4-Alkyl,
- R2 Wasserstoff oder C1-C4-Alkyl und
- n Zahlen von 0 bis 6 bedeuten sowie
- d) 5 - 20 % eines oder mehrerer Polyglykoläther der Formel III
- wobei R C8-C18-Alkyl oder Alkenyl und
- n Zahlen von 3 - 12 bedeuten
- und der an 100 Gewichts-% fehlende Rest ist Wasser.
- 8 - 12 % Paraffin (Fp 50 - 53° C),
- 3 - 6 % eines Imidazolins der Formel I, wobei R C12-C18-Alkyl, R1 C16-C22-Acyl, R2 Wasserstoff,
- X- Cl- oder CH3COO- und
- n 2 oder 3 bedeuten,
- 3 - 5 % eines Aminoxids der Formel II, wobei
- R C8-C18-Alkyl oder Alkenyl,
- R und R2 Methyl und
- n Null bedeuten
- 6 - 10 % eines Polyglykoläthers der Formel III, wobei R Cocosalkyl (C12-C18-Alkyl und Alkenyl), n Zahlen von 4 - 8 bedeuten, und der an 100 Gew.% fehlende Rest ist Wasser.
- a) 5 - 20% paraffin, melting range 45 - 60 ° C
- b) 2-10% of one or more alkylimidazolines of the formula I.
- where RC 12 -C 22 alkyl, alkenyl or hydroxyalkyl,
- R 1 is hydrogen or C 1 -C 22 -saturated or unsaturated aliphatic or aromatic acyl,
- R 2 is hydrogen, C 1 -C 4 alkyl or hydroxyalkyl, n numbers from 2 - 6 and
- X is a halogen, C 1 -C 4 alkyl sulfate, C 1 -C 4 dialkyl phosphate or a C 1 -C 4 alkyl carboxylate anion.
- c) 1-5% of one or more amine oxides of the general formula II
- where RC 8 -C 12 alkyl or alkenyl,
- R 1 C 1 -C 4 alkyl,
- R2 is hydrogen or C 1 -C 4 alkyl and
- n numbers from 0 to 6 mean as well
- d) 5-20% of one or more polyglycol ethers of the formula III
- where RC 8 -C 18 alkyl or alkenyl and
- n mean numbers from 3 to 12
- and the rest missing in 100% by weight is water.
- 8 - 12% paraffin (mp 50 - 53 ° C),
- 3 - 6% of an imidazoline of the formula I, where R C 12 -C 18 alkyl, R 1 C 16 -C 22 acyl, R 2 is hydrogen,
- X - Cl - or CH 3 COO - and
- n is 2 or 3,
- 3-5% of an amine oxide of the formula II, where
- R C 8 -C 18 alkyl or alkenyl,
- R and R 2 are methyl and
- n mean zero
- 6 - 10% of a polyglycol ether of the formula III, wherein R coconut alkyl (C 12 -C 18 alkyl and alkenyl), n is from 4 -. 8 mean, and to 100% by weight missing remainder being water.
Die Herstellung der Paraffindispersion erfolgt durch intensives Mischen aller Komponenten bei Temperaturen von über 70 - 80° C, wobei als besonderer Vorteil hervorzuheben ist, dass man keinen Homogenisator benötigt.The paraffin dispersion is produced by intensive mixing of all components at temperatures of above 70-80 ° C., a particular advantage being that no homogenizer is required.
Die klaren Dispersionen sind stabil und können mit kaltem Wasser auf die gewünschte Endkonzentration in einer wässrigen Flotte verdünnt werden. Diese Paraffindispersionen, die beim Verdünnen mit Wasser lager- und scherstabile Feindispersionen bilden, können anstelle von festem Trockenparaffin zum Paraffinieren von Stapelfasergarnen aus nativen und synthetischen Fasern eingesetzt werden. Sie können als pseudokationisch dispergierte Systeme bezeichnet werden und zeichnen sich durch hohe Substantivität beim Einsatz in langer Flotte aus. Der pH-Wert der Paraffindispersionen liegt beim Einsatz vorteilhaft bei 3 - 6 und wird mit Säuren auf diesen Wert eingestellt.The clear dispersions are stable and can be diluted with cold water to the desired final concentration in an aqueous liquor. These paraffin dispersions, which form fine dispersions that are stable in storage and shear when diluted with water, can be used instead of solid dry paraffin for the paraffin waxing of staple fiber yarns from native and synthetic fibers. They can be called pseudo-cationically dispersed systems and are characterized by high substantivity when used in a long fleet. When used, the pH of the paraffin dispersions is advantageously 3 - 6 and is adjusted to this value with acids.
Die Applikation der Paraffindispersionen erfolgt in üblichen Färbeapparaten, wie sie zum Färben von Textilgarnen verwendet werden. Gearbeitet wird dabei in Flottenverhältnissen von 1 : 5 bis 1 : 40 bei Temperaturen von 10 - 90° C. Vorteilhaft erfolgt die Applikation nach dem Färbeprozess, indem man nach dem Spülen das Garn mit einer Dispersion der oben beschriebenen Art in verdünnter wässriger Form behandelt, die 0,1 - 2 Gew.%, vorzugsweise 0,3 - 1 Gew.% des Mittels der oben beschriebenen Zusammensetzung, bezogen auf das Garngewicht enthält.The paraffin dispersions are applied in customary dyeing machines such as those used for dyeing textile yarns. The process is carried out in liquor ratios of 1: 5 to 1:40 at temperatures of 10 - 90 ° C. The application is advantageously carried out after the dyeing process, by rinsing the yarn with a dispersion of the type described above in a dilute aqueous form delt, which contains 0.1-2% by weight, preferably 0.3-1% by weight, of the composition of the composition described above, based on the weight of the yarn.
Die auf diese Weise paraffinierten Garne zeigen neben der gewünschten Glätte einen angenehmen weichen Griff, der die Applikation eines zusätzlichen Weichmachers überflüssig macht. Durch die in den Systemen eingebauten Dispergiermittel kommt es zu keiner, das Stricken störenden elektrostatischen Aufladung. Die erfindungsgemässen Paraffindisersionen enthalten auch keine organischen Solventien, die für die Umwelt, besonders beim Arbeiten in offenen Apparaten, schädlich sein könnten. Sie enthalten als Gleitkomponente lediglich das wohlfeile Paraffin und benötigen für die Glättevermittlung und den Weichmachungseffekt keine zusätzlichen Komponenten, wie z.B. Fettsäureester, die im Vergleich zu Paraffin teuer sind. Die erfindungsgemässen Paraffindispersionen zeigen eine hohe Substantivität, verbunden mit einer hohen Netzkraft, die die Applikation auch in kurzen Versuchszeiten und bei niederer Temperatur ermöglicht.In addition to the desired smoothness, the yarns paraffinized in this way have a pleasantly soft feel, which makes the application of an additional plasticizer unnecessary. Due to the dispersing agents built into the systems, there is no electrostatic charge interfering with knitting. The paraffin dispersions according to the invention also do not contain any organic solvents which could be harmful to the environment, especially when working in open apparatus. They only contain the inexpensive paraffin as a sliding component and do not require any additional components for conveying smoothness and the softening effect, e.g. Fatty acid esters, which are expensive compared to paraffin. The paraffin dispersions according to the invention have a high substantivity, combined with a high wetting power, which enables application even in short test times and at a low temperature.
Die erfindungsgemässen Dispersionen verleihen Garnen einen hohen Antistatikeffekt verbunden mit hoher Glätte.The dispersions according to the invention give yarns a high antistatic effect combined with high smoothness.
Die Herstellung der in den folgenden Beispielen beschriebenen Dispersionen erfolgt durch einfaches Vermischen der einzelnen Komponenten. Prozentangaben sind als Gewichtsprozent zu verstehen. EO bedeutet Ethylenoxid.The dispersions described in the following examples are prepared by simply mixing the individual components. Percentages are to be understood as percentages by weight. EO means ethylene oxide.
Paraffindispersion bestehend aus 15 Teile Paraffin (Fp. 50 - 53° C), 5 Teile eines Imidazolins der Formel I, wobei R ein Gemisch aus 45 % C15 und 55 % C17-Alkyl, R ein Gemisch aus 45 % C16 und 55 % C18-Acyl, R2 Wasserstoff, n 2 X CH3CO2 bedeutet, 4 Teile Cocosalkyldimethylaminoxid, 10 Teile Cocosfettalkohol x 5 EO, 100 Teile E-Wasser. pH-Wert: ca. 4Paraffin dispersion consisting of 15 parts of paraffin (mp. 50-53 ° C.), 5 parts of an imidazoline of the formula I, where R is a mixture of 45% C 15 and 55% C 17 alkyl, R is a mixture of 45% C16 and 55 % C 18 acyl, R 2 is hydrogen, n 2 X CH 3 CO 2 , 4 parts of cocoalkyldimethylamine oxide, 10 parts of coconut fatty alcohol x 5 EO, 100 parts of deionized water. pH value: approx. 4
Paraffindispersion bestehend aus 17 Teile Paraffin (Fp. 50 - 53° C), 7 Teile des Imidazolins nach Beispiel 1 4 Teile Oleyldiethylaminoxid, 8 Teile Oleylalkohol x 7 EO, 100 Teile E-Wasser. pH-Wert: ca. 4,2Paraffin dispersion consisting of 17 parts of paraffin (mp. 50-53 ° C.), 7 parts of the imidazoline according to Example 1, 4 parts of oleyl diethylamine oxide, 8 parts of oleyl alcohol x 7 EO, 100 parts of deionized water. pH: approx.4.2
Paraffindispersion bestehend aus 13 Teile Paraffin (Fp. 52 - 54° C), 6 Teile eines Imidazolins der Formel I, wobei R ein Gemisch aus 5 % C13, 30 % C15' 35 % C17-Alkyl und 30 % C17-Alkenyl, R1 ein Gemisch aus 5 % C14, 30 % C16, 35 % C18-Acyl und 30 % C1$-Acenyl, R2 Wasserstoff, n 2 und X Acetat bedeutet, 3 Teile eines Aminoxid der Formel II, wobei R ein Gemisch aus 70 % C12 und 30 % C14-Alkyl, R1 und R2 Methyl und n 0 bedeutet und 6 Teile Cocosfettalkohol x 6 EO 6 Teile Oleylalkohol x 5 EO 100 Teile E-Wasser. pH-Wert: 4,5Paraffin dispersion consisting of 13 parts paraffin (mp 52-54 ° C), 6 parts of an imidazoline of the formula I, where R is a mixture of 5% C 13 , 30% C 15 '35% C 17 alkyl and 30% C 17 -Alkenyl, R 1 is a mixture of 5% C 14 , 30% C 16 , 35% C 18 -acyl and 30% C 1 $ -acenyl, R 2 is hydrogen, n 2 and X acetate, 3 parts of an amine oxide of the formula II, where R is a mixture of 70% C12 and 30% C 14 alkyl, R 1 and R 2 is methyl and n 0 and 6 parts of coconut fatty alcohol x 6 EO 6 parts oleyl alcohol x 5 EO 100 parts of demineralized water. pH: 4.5
Paraffindispersion bestehend aus 14 Teile Paraffin (Fp. 52 - 54° C), 2,4 Teile des in Beispiel 1 verwendeten Imidazolins, 0,6 Teile eines Imidazolins der Formel I, wobei R ein Gemisch aus 5 % C13' 30 % C15' 35 % C17-Alkyl und 30 % C17-Alkenyl, R1 und R2 Wasserstoff, n 2 und X CH3COO- bedeutet, 6 Teile Cocosalkyldimethylaminoxid und 10 Teile C12/C14-Alkohol x 10 EO, 100 Teile E-Wasser. pH-Wert: 4,1Paraffin dispersion consisting of 14 parts of paraffin (mp. 52-54 ° C.), 2.4 parts of the imidazoline used in Example 1, 0.6 part of an imidazoline of the formula I, where R is a mixture of 5% C 13-30 % C. 15 '35% C 17 alkyl and 30% C 17 alkenyl, R 1 and R 2 hydrogen, n 2 and X CH 3 COO - means 6 parts cocoalkyldimethylamine oxide and 10 parts C 12 / C 14 alcohol x 10 EO, 100 parts of demineralized water. pH: 4.1
In einem Kreuzspulfärbeapparat wurden unter HT-Bedingungen Garne aus 100 %igem PES nach vorangegangener Dispersionsfärbung und Spülen bei 40° C 30 Minuten lang im Flottenverhältnis 1 : 10 bei pH 5,5 mit den in den Beispielen 1 - 4 beschriebenen Dispersionen in verdünnter Form behandelt. Diese Dispersionen wurden soweit verdünnt, dass die Konzentration der Komponenten a) bis d) in der Flotte, bezogen auf das Garngewicht, 2 Gew.% betrug. Nach dem Trocknen wies das PES-Material einen glatten weichen Griff auf, wie er für trockenparaffinierte Garne nur unter Zusatz eines kationischen Weichmachers zu erzielen ist.Yarns made from 100% PES were treated in a cross-wound dyeing machine under HT conditions after previous dispersion dyeing and rinsing at 40 ° C. for 30 minutes in a liquor ratio 1:10 at pH 5.5 with the dispersions described in Examples 1-4 in dilute form . These dispersions were diluted to such an extent that the concentration of components a) to d) in the liquor, based on the weight of the yarn, was 2% by weight. After drying, the PES material had a smooth, soft feel, which can only be achieved for dry-waxed yarns with the addition of a cationic softener.
Die Glätte der nassparaffinierten Garne ist sehr hoch. Der Reibungskoeffizient, gemessen in der DE-OS 24 16 430 besc beschriebenen Messanordnung, ergab bei den Messgeschwindigkeiten 20 und 100 m/Minute folgende Werte:
An den Strickwaren wurden folgende Antistatikwerte in Meg-Ohm bei 22° C und 65 % r. F. gemessen:
Ähnlich günstige Effekte werden erzielt, wenn anstelle von PES-Garnen, Wollgarne, Baumwollgarne oder PAC-Garne oder Mischungen eingesetzt werden.Similar favorable effects are achieved if instead of PES yarns, wool yarns, cotton yarns or PAC yarns or blends are used.
Claims (3)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2927027 | 1979-07-04 | ||
| DE19792927027 DE2927027A1 (en) | 1979-07-04 | 1979-07-04 | AGENT FOR LIQUID PARAFFINING YARN |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0022239A1 true EP0022239A1 (en) | 1981-01-14 |
| EP0022239B1 EP0022239B1 (en) | 1982-12-22 |
Family
ID=6074906
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP80103725A Expired EP0022239B1 (en) | 1979-07-04 | 1980-07-01 | Agent and process for wet paraffinic treatment of yarns |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US4322302A (en) |
| EP (1) | EP0022239B1 (en) |
| JP (1) | JPS569473A (en) |
| DE (2) | DE2927027A1 (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0075261A3 (en) * | 1981-09-17 | 1985-01-30 | Hoechst Aktiengesellschaft | Preparing agent for fibres |
| EP0103331A3 (en) * | 1982-09-09 | 1985-03-27 | Wool Research Organisation Of New Zealand Inc. | Antistatic composition |
| AU602309B2 (en) * | 1985-08-01 | 1990-10-11 | Procter & Gamble Company, The | Dispersible fabric softeners |
| EP0416917A3 (en) * | 1989-09-07 | 1991-08-28 | Kao Corporation | Spinning lubricant composition for acrylic fibre |
| WO2000001875A1 (en) * | 1998-07-03 | 2000-01-13 | Cognis Deutschland Gmbh | Softening composition |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2482636A1 (en) | 1980-05-14 | 1981-11-20 | Lesieur Cotelle Et Associes Sa | CONCENTRATED SOFTENING COMPOSITION FOR TEXTILE FIBERS |
| DE3028016A1 (en) | 1980-07-24 | 1982-02-25 | Hoechst Ag, 6000 Frankfurt | PREPARATION AGENTS FOR SYNTHESIS FIBERS AND THE USE THEREOF |
| DE3115679A1 (en) | 1981-04-18 | 1982-10-28 | Th. Goldschmidt Ag, 4300 Essen | SUBSTANTIVE PREPARATION AGENT FOR YARNS OR TWINS |
| RU2222653C1 (en) * | 2002-05-28 | 2004-01-27 | Ивановский государственный химико-технологический университет | Composition for treatment of textile fibers and yarn |
| RU2230141C1 (en) * | 2002-11-29 | 2004-06-10 | Открытое акционерное общество "КАНАТ" | Method for processing of cordage and rope products and composition for pro cessing the same |
| RU2321692C2 (en) * | 2005-07-25 | 2008-04-10 | Общество с ограниченной ответственностью "Фишеринг Сервис" | Method of and device for treatment of cordage and treatment compound |
| RU2346091C1 (en) * | 2007-05-25 | 2009-02-10 | Открытое акционерное общество "КАНАТ" | Composition for treatment of cordage and method of its application |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1239057B (en) | 1960-05-02 | 1967-04-20 | Monsanto Co | Process for improving the properties of threads made from synthetic linear polymers |
| FR2230790A1 (en) | 1973-05-26 | 1974-12-20 | Hoechst Ag | |
| FR2322963A1 (en) | 1975-09-04 | 1977-04-01 | Hoechst Ag | SOFTENERS FOR TEXTILE MATERIALS |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE699028C (en) * | 1937-03-10 | 1940-11-21 | I G Farbenindustrie Akt Ges | Softening of textile goods |
| US2974106A (en) * | 1955-12-02 | 1961-03-07 | Comcolloid Inc | Emulsifier-wax compositions |
| US2995520A (en) * | 1956-06-11 | 1961-08-08 | Nalco Chemical Co | Treatment of fibrous materials and compositions therefor |
-
1979
- 1979-07-04 DE DE19792927027 patent/DE2927027A1/en not_active Withdrawn
-
1980
- 1980-06-30 US US06/164,036 patent/US4322302A/en not_active Expired - Lifetime
- 1980-07-01 EP EP80103725A patent/EP0022239B1/en not_active Expired
- 1980-07-01 DE DE8080103725T patent/DE3061423D1/en not_active Expired
- 1980-07-03 JP JP9003780A patent/JPS569473A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1239057B (en) | 1960-05-02 | 1967-04-20 | Monsanto Co | Process for improving the properties of threads made from synthetic linear polymers |
| FR2230790A1 (en) | 1973-05-26 | 1974-12-20 | Hoechst Ag | |
| FR2322963A1 (en) | 1975-09-04 | 1977-04-01 | Hoechst Ag | SOFTENERS FOR TEXTILE MATERIALS |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0075261A3 (en) * | 1981-09-17 | 1985-01-30 | Hoechst Aktiengesellschaft | Preparing agent for fibres |
| EP0103331A3 (en) * | 1982-09-09 | 1985-03-27 | Wool Research Organisation Of New Zealand Inc. | Antistatic composition |
| AU602309B2 (en) * | 1985-08-01 | 1990-10-11 | Procter & Gamble Company, The | Dispersible fabric softeners |
| EP0416917A3 (en) * | 1989-09-07 | 1991-08-28 | Kao Corporation | Spinning lubricant composition for acrylic fibre |
| US5282871A (en) * | 1989-09-07 | 1994-02-01 | Kao Corporation | Spinning lubricant composition for acrylic fiber |
| WO2000001875A1 (en) * | 1998-07-03 | 2000-01-13 | Cognis Deutschland Gmbh | Softening composition |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0022239B1 (en) | 1982-12-22 |
| DE3061423D1 (en) | 1983-01-27 |
| JPS569473A (en) | 1981-01-30 |
| US4322302A (en) | 1982-03-30 |
| DE2927027A1 (en) | 1981-01-08 |
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