CA2080741A1 - Biodegradable spin finishes - Google Patents
Biodegradable spin finishesInfo
- Publication number
- CA2080741A1 CA2080741A1 CA002080741A CA2080741A CA2080741A1 CA 2080741 A1 CA2080741 A1 CA 2080741A1 CA 002080741 A CA002080741 A CA 002080741A CA 2080741 A CA2080741 A CA 2080741A CA 2080741 A1 CA2080741 A1 CA 2080741A1
- Authority
- CA
- Canada
- Prior art keywords
- spin
- biodegradable
- compounds
- formula
- spin finish
- 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.)
- Abandoned
Links
- 150000001875 compounds Chemical class 0.000 claims abstract description 17
- 239000000835 fiber Substances 0.000 claims abstract description 7
- 238000000034 method Methods 0.000 claims abstract description 6
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 4
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 3
- 239000000314 lubricant Substances 0.000 claims description 3
- 238000012360 testing method Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000008030 elimination Effects 0.000 description 3
- 238000003379 elimination reaction Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 229920002994 synthetic fiber Polymers 0.000 description 3
- 239000012209 synthetic fiber Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000010696 ester oil Substances 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 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
- HSRJKNPTNIJEKV-UHFFFAOYSA-N Guaifenesin Chemical compound COC1=CC=CC=C1OCC(O)CO HSRJKNPTNIJEKV-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000006065 biodegradation reaction Methods 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- -1 ester salts Chemical class 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000010801 sewage sludge Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000011282 treatment 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
- D06M13/10—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
- D06M13/17—Polyoxyalkyleneglycol 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
- 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
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2904—Staple length fiber
- Y10T428/2907—Staple length fiber with coating or impregnation
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2967—Synthetic resin or polymer
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2967—Synthetic resin or polymer
- Y10T428/2969—Polyamide, polyimide or polyester
Abstract
Abstract of the disclosure:
Biodegradable spin finishes The invention relates to spin finishes which contain compounds of the formula HO(CH2CH20)x-RO-(CH2CH2O)yH I
in which R is an alkylene radical which is mono- or poly-substituted by alkyl, has 2 to 4 carbon atoms in the alkylene chain and contains methyl, ethyl, propyl or isopropyl as the alkyl substituent, and the sum of x and y is 10 to 20, x and y being different from zero, and to a process for the spin finishing of fibers.
Biodegradable spin finishes The invention relates to spin finishes which contain compounds of the formula HO(CH2CH20)x-RO-(CH2CH2O)yH I
in which R is an alkylene radical which is mono- or poly-substituted by alkyl, has 2 to 4 carbon atoms in the alkylene chain and contains methyl, ethyl, propyl or isopropyl as the alkyl substituent, and the sum of x and y is 10 to 20, x and y being different from zero, and to a process for the spin finishing of fibers.
Description
20~07~1 ~OE~HST A~TI~NGESELLSC~AFT HOE 91/F 3~8 Dr.Kl/rh Description Biodegradable spin fini~hes US-A-4,179,544 and US-~-4,227,390 di~close, polyoxy-alkylene glycols which, in a heat treatment of spin finished synthetic fibers, such as texturing, evaporate without leaving a residue, 80 that, when using the~ in spin finishes, the intervals at which the texturin~ means used are cleaned are relatively long. EP-B-162,530 dis-closes end-capped polyoxyalkylene glycols which have goods properties as spin finishes and are also distingui-shed by low re~idue formation on the fiber after heating processes.
However, the great disadvantage of all these compounds is their only moderate biodegradability. In recent years, additional demands have been made on spin finishes to the effect that they should be readily biodegradable in the waste water. The ob~ective of the~e demands is to eliminate the spin finishes entering the waste water of textile plants during dyeing or pretreatment by biodegradation. The term "biodegradable~ is to be under-stood as meaning that the components of spin finishes, ~uch as lubricants, surfactants, yarn cohesifiers or else antistats, are biodegraded completely or at least to the extent of 70% by weight, for example by the enzymes or bacteria present in the sewage sludge of a water treat-ment plant. It is desirable that thi~ degradation produce chemically simple compounds, such as carbon dioxide, water, ~ulfate or phosphate.
A number of test procedures have been developed for evaluating the biodegradability of chemical compounds.
The "coupled units test" (OECD 303 A Test) is mentioned as a suitable method for testing the biodegradability of spin finishes.
20~074~
It is still very difficult to prepare biodegradable spin fini~hes. This i8 what the invention seeks to remedy.
The invention relates to spin finishes compri~ing compounds of the formula HO(CH2CH20)S-RO-(CH2CH2)~H
in which R is an alkylene radical which is mono- or poly-sub~tituted by alkyl, has 2 to 4 carbon atoms in the alkylene chain and contains methyl, ethyl, propyl or isopropyl as the alkyl substituent, and the 8um of x and y is 10 to 20, x and y being different from zero.
Preferred components of these biodegrsdable spin finishes are compounds of the formula I in which R is a l-methyl-propylene radical, 2-methylpropylene radical or a 2,2-dimethylpropylene radical, particularly preferably a 1-methylethylene radical (isopropylene radical).
These compounds of the formula I are prepared by the process described in EP-B-166,958 by reacting a glycol with ethylene oxide.
Owing to their unexpectedly low residue formation in heating processes, such a~ texturing, and their surprisingly good biodegradability, the compounds of the formula I are highly suitable for use a8 spin finishes.
However, the great disadvantage of all these compounds is their only moderate biodegradability. In recent years, additional demands have been made on spin finishes to the effect that they should be readily biodegradable in the waste water. The ob~ective of the~e demands is to eliminate the spin finishes entering the waste water of textile plants during dyeing or pretreatment by biodegradation. The term "biodegradable~ is to be under-stood as meaning that the components of spin finishes, ~uch as lubricants, surfactants, yarn cohesifiers or else antistats, are biodegraded completely or at least to the extent of 70% by weight, for example by the enzymes or bacteria present in the sewage sludge of a water treat-ment plant. It is desirable that thi~ degradation produce chemically simple compounds, such as carbon dioxide, water, ~ulfate or phosphate.
A number of test procedures have been developed for evaluating the biodegradability of chemical compounds.
The "coupled units test" (OECD 303 A Test) is mentioned as a suitable method for testing the biodegradability of spin finishes.
20~074~
It is still very difficult to prepare biodegradable spin fini~hes. This i8 what the invention seeks to remedy.
The invention relates to spin finishes compri~ing compounds of the formula HO(CH2CH20)S-RO-(CH2CH2)~H
in which R is an alkylene radical which is mono- or poly-sub~tituted by alkyl, has 2 to 4 carbon atoms in the alkylene chain and contains methyl, ethyl, propyl or isopropyl as the alkyl substituent, and the 8um of x and y is 10 to 20, x and y being different from zero.
Preferred components of these biodegrsdable spin finishes are compounds of the formula I in which R is a l-methyl-propylene radical, 2-methylpropylene radical or a 2,2-dimethylpropylene radical, particularly preferably a 1-methylethylene radical (isopropylene radical).
These compounds of the formula I are prepared by the process described in EP-B-166,958 by reacting a glycol with ethylene oxide.
Owing to their unexpectedly low residue formation in heating processes, such a~ texturing, and their surprisingly good biodegradability, the compounds of the formula I are highly suitable for use a8 spin finishes.
2~ The compounds of the formula I are in general water-~oluble or water-dispersible. They can be used as spin fini~he~ either by themselves or in a mixture with one another or with other spin finish components known per se, such as surfactants, antistats, xuch as P205 ester salts, lubricants, such a~ ester oils, or yarn cohesi-fiers, such as ethoxylated castor oils, which must also be biodegradable.
208~7~1 If a mixture of the compounds of the formula I with known spin finish components is used, the relative amount of the compounds of the formula I should be in the range from 10 to 100 parts by weight, relative to the spin finish. When synthetic fibers are spin finished using compounds of the formula I or mixtures thereof, the add-on should be 0.1 to 1%, preferably 0.3 to 0.5% on weight of fiber, the compounds of the formula I being present in the spin finish in accordance with the percentages given above.
The spin finishe3 can be applied from aqueous solution, dispersion or emulsion, if appropriate with additional use of suitable solvents or dispersants.
Since the ma~ority of the compounds of the formula I are readily water-soluble, they can be applied to the fiber, unlike mineral or ester oils, without the need for addi-tional emulsifiers.
Application takes place by customary methods, for example by face-padding, dipping, spraying, dip-adding or by means of gear pumps.
Examples of suitable synthetic fibers for which the spin finshes are to be used are fibers made of polyesters, polyamides, polyacrylonitrile, polyolefins or copolymers of the abovementioned compounds.
Gsneral procedure for preparing the acetals mentioned belows The amounts of glycol and alkaline catalyst are initially introduced into a reaction vessel equipped with a ~tirrer. After flushing with nitrogen to remove the oxygen, the mixture is heated to 120 to 125C and kept at this temperature under a water pump vacuum for 2 hours with stirring. After removing the water pump vacuum, the mixture is heated to 130 to 140C with stirring, after which the required amount of gaseous ethylene oxide is _ 4 _ 2 0 8 0 7 ~ ~
metered in at this temperature over a period of about 3 hours. The end of ethylene oxide addition i~ ~ndicated by the pre6sure which decreaqes and remains essentially constant. In order to purify the reaction product by removing any volatile components which may be present, it is maintained at about 80 DC and a vacuum of 2 kPa for half an hour with stirring.
The initially introduced glycols and alkaline catalysts and the amount of ethylsne oxide metered in at the reaction temperature and the reaction pressure are ~ummarized in Table I below.
20807~1 Table I
Exan~ Glyeol Ethylene Cata1~st ple oxide te~pe¢~- pre~sure Nc~. (g) ~ l) (q) (~1) Type wei~ht) (C) (l~Pa) 1 1,2-10 ~ , 76.0 1.0 SlO.~ ll.6 ~a~3 l.0 l40-lS0 50-400 ~l ~ ~0-300 3 glyc~l~
_ 76.0 1.0 8B0.0 20.0 _ 2.5 140-150 50-400 l,2_ glyco1~
76.0 ~ 1.0 1276.0 29.0 _ 2.0 120-l40 50-400 i Test of the evaporation rate of Examples 1 to 4:
In the evaporation test, 1 g each of the Examples 1 to 4 listed in Table I are maintained at 220C, and the lo~i3e~
at 0.33 hour (20 minutes) and 24 hours are evaluated.~he losses of Examples 1 to 4 in percent can be seen from Table II.
Table II
Duration Example No. 20 minutes 24 hours 1 9% >95%
2 8% >95%
3 7% >95%
208~7~1 If a mixture of the compounds of the formula I with known spin finish components is used, the relative amount of the compounds of the formula I should be in the range from 10 to 100 parts by weight, relative to the spin finish. When synthetic fibers are spin finished using compounds of the formula I or mixtures thereof, the add-on should be 0.1 to 1%, preferably 0.3 to 0.5% on weight of fiber, the compounds of the formula I being present in the spin finish in accordance with the percentages given above.
The spin finishe3 can be applied from aqueous solution, dispersion or emulsion, if appropriate with additional use of suitable solvents or dispersants.
Since the ma~ority of the compounds of the formula I are readily water-soluble, they can be applied to the fiber, unlike mineral or ester oils, without the need for addi-tional emulsifiers.
Application takes place by customary methods, for example by face-padding, dipping, spraying, dip-adding or by means of gear pumps.
Examples of suitable synthetic fibers for which the spin finshes are to be used are fibers made of polyesters, polyamides, polyacrylonitrile, polyolefins or copolymers of the abovementioned compounds.
Gsneral procedure for preparing the acetals mentioned belows The amounts of glycol and alkaline catalyst are initially introduced into a reaction vessel equipped with a ~tirrer. After flushing with nitrogen to remove the oxygen, the mixture is heated to 120 to 125C and kept at this temperature under a water pump vacuum for 2 hours with stirring. After removing the water pump vacuum, the mixture is heated to 130 to 140C with stirring, after which the required amount of gaseous ethylene oxide is _ 4 _ 2 0 8 0 7 ~ ~
metered in at this temperature over a period of about 3 hours. The end of ethylene oxide addition i~ ~ndicated by the pre6sure which decreaqes and remains essentially constant. In order to purify the reaction product by removing any volatile components which may be present, it is maintained at about 80 DC and a vacuum of 2 kPa for half an hour with stirring.
The initially introduced glycols and alkaline catalysts and the amount of ethylsne oxide metered in at the reaction temperature and the reaction pressure are ~ummarized in Table I below.
20807~1 Table I
Exan~ Glyeol Ethylene Cata1~st ple oxide te~pe¢~- pre~sure Nc~. (g) ~ l) (q) (~1) Type wei~ht) (C) (l~Pa) 1 1,2-10 ~ , 76.0 1.0 SlO.~ ll.6 ~a~3 l.0 l40-lS0 50-400 ~l ~ ~0-300 3 glyc~l~
_ 76.0 1.0 8B0.0 20.0 _ 2.5 140-150 50-400 l,2_ glyco1~
76.0 ~ 1.0 1276.0 29.0 _ 2.0 120-l40 50-400 i Test of the evaporation rate of Examples 1 to 4:
In the evaporation test, 1 g each of the Examples 1 to 4 listed in Table I are maintained at 220C, and the lo~i3e~
at 0.33 hour (20 minutes) and 24 hours are evaluated.~he losses of Examples 1 to 4 in percent can be seen from Table II.
Table II
Duration Example No. 20 minutes 24 hours 1 9% >95%
2 8% >95%
3 7% >95%
4 6% >95%
Biodeqradability test:
The biodegradability is determined by means of the OECD
303 A test. In this test, the biological elimination [% DOC] is determined as a function of time ~d] (d =
day).
Table III indicates the maximum value of biological elimination after 28 days.
Table III
Example No. Biological elimination ~%] Time [d]
1 ~90% 28 2 >90~ 28 3 >90% 28 4 >90% 18
Biodeqradability test:
The biodegradability is determined by means of the OECD
303 A test. In this test, the biological elimination [% DOC] is determined as a function of time ~d] (d =
day).
Table III indicates the maximum value of biological elimination after 28 days.
Table III
Example No. Biological elimination ~%] Time [d]
1 ~90% 28 2 >90~ 28 3 >90% 28 4 >90% 18
Claims (5)
1. A spin finish comprising compounds of the formula H0(CH2CH2O)x-RO-(CH2CH2O)yH I
in which R is an alkylene radical which i9 mono- or poly-substituted by alkyl, has 2 to 4 carbon atoms in the alkylene chain and contains methyl, ethyl, propyl or isopropyl as the alkyl substituent, and the sum of x and y is 10 to 20, x and y being different from zero.
in which R is an alkylene radical which i9 mono- or poly-substituted by alkyl, has 2 to 4 carbon atoms in the alkylene chain and contains methyl, ethyl, propyl or isopropyl as the alkyl substituent, and the sum of x and y is 10 to 20, x and y being different from zero.
2. A spin finish as claimed in claim 1, wherein the content of compounds of the formula I is in the range from 10 to 100 parts by weight, relative to the spin finish.
3. A spin finish as claimed in claim 1 or 2, wherein biodegradable or non-biodegradable antistats, yarn cohesifiers and/or lubricants are present as further components.
4. A spin finish as claimed in one of claims 1 to 3, wherein the biodegradability is above 90% by weight.
5. A process for the spin finishing of fibers, wherein the add-on of a spin finish as claimed in one of claims 1 to 4 is in the range from 0.1 to 1.0% by weight, relative to the weight of the fiber.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4134610 | 1991-10-19 | ||
| DEP4134610.6 | 1991-10-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2080741A1 true CA2080741A1 (en) | 1993-04-20 |
Family
ID=6443017
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002080741A Abandoned CA2080741A1 (en) | 1991-10-19 | 1992-10-16 | Biodegradable spin finishes |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US5266221A (en) |
| EP (1) | EP0538714B2 (en) |
| JP (1) | JP3258724B2 (en) |
| KR (1) | KR930008233A (en) |
| AR (1) | AR247432A1 (en) |
| AT (1) | ATE150108T1 (en) |
| BR (1) | BR9204029A (en) |
| CA (1) | CA2080741A1 (en) |
| DE (1) | DE59208170D1 (en) |
| ES (1) | ES2100997T5 (en) |
| MX (1) | MX9205982A (en) |
| TR (1) | TR26747A (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW225562B (en) * | 1991-10-15 | 1994-06-21 | Hoechst Ag | |
| DE4304354A1 (en) * | 1993-02-13 | 1994-08-18 | Hoechst Ag | Ester compounds, process for their preparation and their use |
| DE4410708C1 (en) * | 1994-03-28 | 1995-07-13 | Hoechst Ag | Aramid fibre with good mechanical, antistatic and processing properties |
| JP3045238B1 (en) * | 1999-03-24 | 2000-05-29 | 日華化学株式会社 | Oil treatment method for fiber and oil treatment method for fiber |
| KR20160108856A (en) | 2015-03-09 | 2016-09-21 | 한국전자통신연구원 | Electromagnetic wave sensor and method for generating the electromagnetic wave sensor |
| CN115852683A (en) * | 2022-11-30 | 2023-03-28 | 上海丰泽源科技有限公司 | Degradable PLA spinning oil and preparation method thereof |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4179544A (en) * | 1977-12-05 | 1979-12-18 | Basf Wyandotte Corporation | Fiber finish compositions |
| US4256589A (en) * | 1978-02-16 | 1981-03-17 | Eastman Kodak Company | Fiber treating compositions comprising (a) blend of random copoly(oxyethylene-oxypropylene)butanols (b) alkali metal sulfur compound and (c) alkali metal organic phosphate compound |
| DE2812443C2 (en) * | 1978-03-22 | 1982-12-02 | Hoechst Ag, 6000 Frankfurt | Polyglycol ether thermal formals and their use as fiber finishes |
| US4198464A (en) * | 1978-05-26 | 1980-04-15 | Basf Wyandotte Corporation | Fiber lubricants based upon ethylene oxide capped polyethers of tetrahydrofuran and ethylene oxide |
| GB2109403B (en) * | 1981-11-27 | 1985-07-17 | Shell Int Research | Alkoxylate textile processing oils |
| JPS60215873A (en) * | 1984-04-06 | 1985-10-29 | 竹本油脂株式会社 | Spinning oil composition of polyester or polyamide fiber yarn |
| DE3420708C1 (en) * | 1984-06-02 | 1985-07-18 | Hoechst Ag, 6230 Frankfurt | Modified polyethylene glycols |
| US4622038A (en) * | 1985-01-28 | 1986-11-11 | Basf Corporation | Low residue fiber spin finishes |
| US4789381A (en) * | 1987-04-27 | 1988-12-06 | Kao Corporation | Fiber treating process and composition used therefor |
| DE3723349C1 (en) * | 1987-07-15 | 1988-08-11 | Goldschmidt Ag Th | Means for finishing fibers or fiber products |
| US5066414A (en) * | 1989-03-06 | 1991-11-19 | The Procter & Gamble Co. | Stable biodegradable fabric softening compositions containing linear alkoxylated alcohols |
| DE3936975C1 (en) * | 1989-11-07 | 1991-01-24 | Tudapetrol Mineraloelerzeugnisse Nils Hansen Kg, 2000 Hamburg, De | Spooling oil to treat textured fibres or yarns - comprises vegetable oil, ester of vegetable fatty acid, fatty alcohol polyglycol ether, fatty alcohol methacrylate, etc. |
| US5079076A (en) * | 1990-03-15 | 1992-01-07 | The Lubrizol Corporation | Composition and polymer fabrics treated with the same |
| US5126060A (en) * | 1991-01-09 | 1992-06-30 | Colgate-Palmolive Co. | Biodegradable fabric softening compositions based on pentaerythritol esters and free of quaternary ammonium compounds |
-
1992
- 1992-10-13 DE DE59208170T patent/DE59208170D1/en not_active Expired - Fee Related
- 1992-10-13 ES ES92117479T patent/ES2100997T5/en not_active Expired - Lifetime
- 1992-10-13 EP EP92117479A patent/EP0538714B2/en not_active Expired - Lifetime
- 1992-10-13 AT AT92117479T patent/ATE150108T1/en not_active IP Right Cessation
- 1992-10-15 US US07/961,445 patent/US5266221A/en not_active Expired - Fee Related
- 1992-10-15 AR AR92323430A patent/AR247432A1/en active
- 1992-10-15 JP JP27752192A patent/JP3258724B2/en not_active Expired - Fee Related
- 1992-10-16 CA CA002080741A patent/CA2080741A1/en not_active Abandoned
- 1992-10-16 MX MX9205982A patent/MX9205982A/en not_active IP Right Cessation
- 1992-10-16 TR TR92/1087A patent/TR26747A/en unknown
- 1992-10-16 BR BR929204029A patent/BR9204029A/en not_active Application Discontinuation
- 1992-10-19 KR KR1019920019161A patent/KR930008233A/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AR247432A1 (en) | 1994-12-29 |
| EP0538714A1 (en) | 1993-04-28 |
| JPH05279924A (en) | 1993-10-26 |
| BR9204029A (en) | 1994-03-22 |
| EP0538714B2 (en) | 1999-09-01 |
| EP0538714B1 (en) | 1997-03-12 |
| TR26747A (en) | 1995-05-15 |
| ATE150108T1 (en) | 1997-03-15 |
| JP3258724B2 (en) | 2002-02-18 |
| US5266221A (en) | 1993-11-30 |
| DE59208170D1 (en) | 1997-04-17 |
| ES2100997T5 (en) | 1999-12-01 |
| MX9205982A (en) | 1993-04-01 |
| KR930008233A (en) | 1993-05-21 |
| ES2100997T3 (en) | 1997-07-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |