EP0075261B1 - Agent pour préparer des fibres - Google Patents
Agent pour préparer des fibres Download PDFInfo
- Publication number
- EP0075261B1 EP0075261B1 EP82108493A EP82108493A EP0075261B1 EP 0075261 B1 EP0075261 B1 EP 0075261B1 EP 82108493 A EP82108493 A EP 82108493A EP 82108493 A EP82108493 A EP 82108493A EP 0075261 B1 EP0075261 B1 EP 0075261B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- alkyl
- fiber
- amine oxides
- preparation
- 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.)
- Expired
Links
- 150000001412 amines Chemical class 0.000 claims description 20
- 238000002360 preparation method Methods 0.000 claims description 19
- 239000000835 fiber Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 239000004753 textile Substances 0.000 claims 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 239000002216 antistatic agent Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 0 C*C1CC(C2)C2C1 Chemical compound C*C1CC(C2)C2C1 0.000 description 4
- 208000034699 Vitreous floaters Diseases 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical group CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000010696 ester oil Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- -1 for example Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Chemical group CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 238000005956 quaternization reaction Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000012207 thread-locking agent Substances 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 238000004018 waxing Methods 0.000 description 1
- 238000004383 yellowing Methods 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
- D06M13/388—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
- preparation agents in the production of filament threads from synthetic polymers is well known and has been sufficiently described.
- a major problem here is the use of antistatic agents, since the components of the preparation must be sufficiently thermostable, especially in filament preparations intended for use on fast-running processing machines. It is known, for example, that classic filament preparations without the addition of antistatic agents exhibit problems with static charging when stretch texturing.
- thermostable antistatic agents for example a quaternization product of the reaction product of diethylaminoethanol with 10 mol of ethylene oxide and 20 mol of propylene oxide.
- the thermal test (230-235 0 C / 24 h.) Indeed shows that these products form only a few residues, but even the remaining residues are too high and can contaminate the heater, especially as the possibly solid residues through reaction with thread guide elements can also cause thread breaks.
- the amine oxides described in DE-A-23 26 966 have proven themselves well in preparation formulations, especially in combinations with low-volatility lubricants, they give the threads good antistatic properties and are to be regarded as thermostable. However, they often have too high a volatility in short-term heating processes, so that when these amine oxides are used alone, the problem of vaporization from the thread can occur too quickly.
- amine oxides based on an oxyalkylated C 4 -C 4 alcohol is also known from EP-A-22 239.
- the agents for liquid paraffin waxing described therein mainly contain paraffin and polyglycol ether and, in addition, even smaller amounts of these amine oxides.
- the invention thus relates to fiber preparation agents which, in addition to the components usually contained in fiber preparation agents, also contain an amine oxide of the formula where R, C 4 ⁇ C 22 alkyl or C 4 ⁇ C 22 alkenyl, preferably C 10 ⁇ C 16 alkyl, R 2 is hydrogen and / or methyl, where hydrogen and methyl can alternate, R 3 and R 4 C, -C 4 alkyl and X is a number from 1 to 20, preferably 3 to 10, contain.
- chain-pure alkyl compounds instead of the chain-pure alkyl compounds, it is of course also possible in any case to use compounds whose alkyl groups represent technical sections, the average number of carbon atoms corresponding to or coming close to the abovementioned alkyl radicals.
- the alkyl residues accumulating from natural long-chain fatty acids are particularly preferred since the corresponding alcohols with one or two long-chain alkyl residues are commercially available and the amine oxides are thus easily accessible.
- the numerical value X is generally an average value, since technical oxyalkylation generally results in product mixtures. This also applies to the oxethylates listed here for the sake of simplicity.
- amine oxides described above are used as antistatic agents in conventional preparation agents.
- these preparation agents usually consist of approx. 20 to 60% by weight of a lubricant such as, for example, ester oils, mineral oils, end-capped oxethylates, propylene-ethylene oxide copolymers, 0-50% by weight emulsifier, for example fatty alcohol oxyethylates, 0-30% by weight.
- a lubricant such as, for example, ester oils, mineral oils, end-capped oxethylates, propylene-ethylene oxide copolymers, 0-50% by weight emulsifier, for example fatty alcohol oxyethylates, 0-30% by weight.
- % other antistakics for example P 2 0 r , esters of fatty alcohols and 1-50% by weight of the amine oxides.
- the amine oxides can be used in combination with thread-locking agents (oxyethylated castor oils, sarcosides, POCI 3 esters) and sliding components (phosphoric acid esters).
- thread-locking agents oxyethylated castor oils, sarcosides, POCI 3 esters
- sliding components phosphoric acid esters
- the amine oxides show a high antistatic effect even in relatively low doses.
- the required quantities fluctuate depending on the type and quantity of the components (oil, emulsifier) and can be easily determined by simple preliminary tests.
- the favorable properties of the amine oxides in the preparation are particularly evident on synthetic fibers such as those made of polyester, polyamide 6, polyamide 6,6, polyacrylonitrile or polyolefin.
- a polyester yarn dtex 300 f 32 matt is spun at 2800m / min, prepared with 12% preparations and on a stretch texturing machine using the friction process on dtex 167 at 800 m / min. stretch textured.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Claims (3)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3136941 | 1981-09-17 | ||
DE19813136941 DE3136941A1 (de) | 1981-09-17 | 1981-09-17 | Faserpraeparationsmittel |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0075261A2 EP0075261A2 (fr) | 1983-03-30 |
EP0075261A3 EP0075261A3 (en) | 1985-01-30 |
EP0075261B1 true EP0075261B1 (fr) | 1987-04-15 |
Family
ID=6141917
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP82108493A Expired EP0075261B1 (fr) | 1981-09-17 | 1982-09-15 | Agent pour préparer des fibres |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0075261B1 (fr) |
JP (1) | JPS5860067A (fr) |
DE (2) | DE3136941A1 (fr) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4025731A1 (de) * | 1990-08-14 | 1992-02-20 | Henkel Kgaa | Textilausruestungsmittel |
AT396930B (de) * | 1992-01-23 | 1993-12-27 | Chemiefaser Lenzing Ag | Aminoxide |
DE19755047A1 (de) * | 1997-12-11 | 1999-06-17 | Hoechst Trevira Gmbh & Co Kg | Vliese aus Elektretfasern mit verbesserter Ladungsstabilität, präparierte Faser, vorzugsweise Elektretfaser, Verfahren zu deren Herstellung und ihre Verwendung |
CN114775276B (zh) * | 2022-05-30 | 2023-03-10 | 宁波润禾高新材料科技股份有限公司 | 一种耐久型两性脂肪族液体亲水柔软剂及其制备方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2000142A1 (fr) * | 1968-01-11 | 1969-08-29 | Armour Ind Chem Co | |
NL7015335A (en) * | 1970-10-20 | 1971-03-25 | Low density washing powders | |
DE2927027A1 (de) * | 1979-07-04 | 1981-01-08 | Hoechst Ag | Mittel zum fluessigparaffinieren von garnen |
-
1981
- 1981-09-17 DE DE19813136941 patent/DE3136941A1/de not_active Withdrawn
-
1982
- 1982-09-15 DE DE8282108493T patent/DE3276076D1/de not_active Expired
- 1982-09-15 EP EP82108493A patent/EP0075261B1/fr not_active Expired
- 1982-09-16 JP JP57159750A patent/JPS5860067A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
EP0075261A3 (en) | 1985-01-30 |
DE3276076D1 (en) | 1987-05-21 |
DE3136941A1 (de) | 1983-04-14 |
JPS5860067A (ja) | 1983-04-09 |
EP0075261A2 (fr) | 1983-03-30 |
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