EP0576896A2 - Veredlungszusammensetzung für Polypropylenfasern - Google Patents
Veredlungszusammensetzung für Polypropylenfasern Download PDFInfo
- Publication number
- EP0576896A2 EP0576896A2 EP93109508A EP93109508A EP0576896A2 EP 0576896 A2 EP0576896 A2 EP 0576896A2 EP 93109508 A EP93109508 A EP 93109508A EP 93109508 A EP93109508 A EP 93109508A EP 0576896 A2 EP0576896 A2 EP 0576896A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- fibres
- condensation product
- fact
- comprised
- fiber
- 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.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 25
- -1 polypropylene Polymers 0.000 title abstract description 9
- 239000004743 Polypropylene Substances 0.000 title abstract description 6
- 229920001155 polypropylene Polymers 0.000 title abstract description 6
- 239000007859 condensation product Substances 0.000 claims abstract description 16
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 16
- 239000000194 fatty acid Substances 0.000 claims abstract description 16
- 229930195729 fatty acid Natural products 0.000 claims abstract description 16
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 16
- LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000000835 fiber Substances 0.000 claims description 28
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 8
- 239000000047 product Substances 0.000 claims description 8
- 239000002202 Polyethylene glycol Substances 0.000 claims description 7
- 229920001223 polyethylene glycol Polymers 0.000 claims description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000003760 tallow Substances 0.000 claims description 6
- 238000009833 condensation Methods 0.000 claims description 5
- 230000005494 condensation Effects 0.000 claims description 5
- 150000002191 fatty alcohols Chemical class 0.000 claims description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 4
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 claims description 4
- 235000021355 Stearic acid Nutrition 0.000 claims description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 3
- 229920000098 polyolefin Polymers 0.000 claims description 3
- 239000008117 stearic acid Substances 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 2
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 2
- 239000004745 nonwoven fabric Substances 0.000 abstract description 7
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 230000002209 hydrophobic effect Effects 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000002390 adhesive tape Substances 0.000 description 3
- 125000005600 alkyl phosphonate group Chemical group 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 239000002216 antistatic agent Substances 0.000 description 2
- 238000003490 calendering Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229940024463 silicone emollient and protective product Drugs 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 description 1
- XXMBEHIWODXDTR-UHFFFAOYSA-N 1,2-diaminoethanol Chemical compound NCC(N)O XXMBEHIWODXDTR-UHFFFAOYSA-N 0.000 description 1
- SSZWWUDQMAHNAQ-UHFFFAOYSA-N 3-chloropropane-1,2-diol Chemical compound OCC(O)CCl SSZWWUDQMAHNAQ-UHFFFAOYSA-N 0.000 description 1
- SJZRECIVHVDYJC-UHFFFAOYSA-N 4-hydroxybutyric acid Chemical compound OCCCC(O)=O SJZRECIVHVDYJC-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- IWYDHOAUDWTVEP-UHFFFAOYSA-N R-2-phenyl-2-hydroxyacetic acid Natural products OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 229960002510 mandelic acid Drugs 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000004753 textile Substances 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
- D06M13/467—Compounds containing quaternary nitrogen atoms derived from polyamines
-
- 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
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
-
- 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
- D06M13/368—Hydroxyalkylamines; Derivatives thereof, e.g. Kritchevsky bases
-
- 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
- D06M13/405—Acylated polyalkylene polyamines
-
- 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 present invention relates to a finish composition, particularly for polyolefine fibres. It relates also to a fiber finish process which uses the above mentioned composition.
- Thermosealing polypropylene fibres are widely used in the hygienic-sanitary field in the manufacture of calendered non-woven fabrics for coverstocks, overalls, monouse sheets.
- a marked hydrophobic characteristic is requested to the non-woven fabric: for example, it is requested to be possible to manufacture non-woven fabrics having a high barrier capacity towards aqueous liquids.
- the measure of the hydrophobic capacity is carried out on fiber staples measuring the "sinking time", that is the time necessary so that the staple, placed in water in a wide mesh basket, sinks under the liquid surface of a little tank filled with water (ASTM method D 1117-58).
- the polypropylene fiber in that wholly olefinic, is as such hydrophobic.
- the industrial processes for producing the fiber and for transfiorming it into finished manufactured product involve necessarily the addition, on the fiber surface, of surface active agents, slipping agents, antistatic agents, in the step of the process named finish.
- the presence of the agents substantially modifies the surface characteristics of the fiber and therefore the "sinking time" also.
- hydrophilic/hydrophobic degree of the fiber is, as a matter of fact, industrially adjusted by the use of specific surface active agents.
- the present state of the art is to finish the fiber with a mixture of silicone products, which give hydrophobic capacity and lubrication, and surface active antistatic agents, such as for example, esters such as alkyl phosphates, which give antistatic capacity without interferring with the hydrophobic degree.
- silicone compounds are used as release-agents.
- Object of the present invention is to provide a finish composition free of silicone additives, and which allows to solve the above mentioned problem relating to the insufficient adhesion without compromising in any way the hydrophobic capacity and the processability of the fiber.
- the finish composition comprises, in mixture or separated each from the other, a condensation product (A) of a fatty acid with a polyalkylenamine, quaternized with the condensation product of a chlorhydrin with polyethylene glycol, and a condensation product (B) of a hydrogenated fatty acid and an aminoalkylalkanolamine (also named hydroxyalkylenediamine), neutralized with an alpha-hydroxycarboxylic acid, added with a polyoxyethylated fatty alcohol.
- the component (B) alone shows better antistatic characteristics but not sufficient hydrophoby.
- components (A) and (B) are used in mixture each other, their weight ratio is preferably comprised between 35/65 and 60/40.
- the level or total concentration of finishing agents on the fiber is preferably comprised between 0.3 and 0.6% by weight, more preferably between 0.4 and 0.5% by weight.
- the fatty acid used in the condensation to obtain the component (A) is preferably a saturated C16-C20, more preferably stearic acid.
- the saturated fatty acid is preferably condensed with tetraethylpentamine.
- the chlorohydrin used to obtain the condensation product with polyethylene glycol able to act as crosslinking and quaternizing agent in the preparation of the component (A) is preferably bis-chlorohydrin ether.
- the condensation product between the polyethylene glycol and the chlorohydrin is present, in the component (A) in a small concentration preferably comprised between 0.5 and 5% by weight.
- the fatty acid used in the condensation reaction to obtain the component (B) is preferably a fatty acid obtained by hydrolysis of tallow, whereas the aminoalkylakanolamine is preferably aminoethylethanolamine.
- the alpha-hydroxycarboxylic acid used to neutralize the condensation product of the hydrogenated fatty acid with the aminoalkylalkanolamine is preferably selected from the group which consists of glycolic acid, mandelic acid, lactic acid, hydroxybutyric acid and mixtures thereof. More preferably glycolic acid is used.
- the polyoxyethylated fatty acid used in the preparation of the component (B) as emulsifier is preferably a fatty alcohol deriving from tallow, condensed with ethylene oxide; for each mol of fatty alcohol 15 mols of ethylene oxide are preferably used.
- the present invention has as object also a fiber finish process which compises the treatment of the fiber with the product (A) only as above defined in aqueous solution at a concentration preferably comprised between 5 and 30 g/l in such a way to leave on the fibres an active residue comprised between 0.005 and 0.05% by weight, and the subsequent treatment of the fiber with a mixture of the products (A) and (B) as above defined in a weight ratio (A)/(B) comprised between 30/70 and 60/40 and at a such concentration to leave on the fiber an active residue comprised between 0.1 and 0.8% by weight.
- a polypropylene fiber obtained by spinning on an industrial plant has been subjected to finish on a pilot plant.
- a product (A) obtained from the condensation of stearic acid with tetraethylenepentamine, with about 1% by weight of polyethylene bis-chlorohydrin as quaternizing and crosslinking agent has been applied.
- the concentration of the product (A) in aqueous bath was equal to 15 g/l, in such a way to leave an active residue on the fiber equal to 0.02% .
- a mixture of the product (A) and of a product (B) obtained from the condensation of fatty acids deriving from hydrogenated tallow with aminoethanolamine, neutralized with glycolic acid and alcohols deriving from tallow condensed with about 15 mols of ethylene oxide as emulsifier agent has been applied.
- the "sinking time" on the staple resulted about 24 hours; the processability of the fiber on textile machines for opening, carding and calendering has resulted good.
- the sinking time on the staple has resulted higher than 48 hours; the processability and adhesion of labels to the non-woven fabric were good.
- the sinking time on the staple has resulted higher than 48 hours; the processability acceptable (slight problems due to the static electricity at the highest working speeds).
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ITMI921625A IT1255205B (it) | 1992-07-03 | 1992-07-03 | Composizione di ensimaggio per fibre polipropileniche |
| ITMI921625 | 1992-07-03 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0576896A2 true EP0576896A2 (de) | 1994-01-05 |
| EP0576896A3 EP0576896A3 (de) | 1994-10-19 |
Family
ID=11363612
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP9393109508A Withdrawn EP0576896A3 (de) | 1992-07-03 | 1993-06-11 | Veredlungszusammensetzung für Polypropylenfasern. |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP0576896A3 (de) |
| JP (1) | JPH06166959A (de) |
| KR (1) | KR940002422A (de) |
| CN (1) | CN1083880A (de) |
| IT (1) | IT1255205B (de) |
| MY (1) | MY131451A (de) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5403426A (en) * | 1991-05-28 | 1995-04-04 | Hercules Incorporated | Process of making cardable hydrophobic polypropylene fiber |
| US5958806A (en) * | 1994-01-14 | 1999-09-28 | Fibervisions A/S | Cardable hydrophobic polyolefin fibres comprising cationic spin finishes |
| WO2009129364A3 (en) * | 2008-04-17 | 2009-12-10 | The Dow Chemical Company | Durable functionalization of polyolefin fibers and fabrics for moisture management and odor control |
| US8092723B2 (en) | 2005-11-18 | 2012-01-10 | Nanocomp Oy Ltd | Method of producing a diffraction grating element |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100456970B1 (ko) * | 2001-12-31 | 2004-11-10 | 주식회사 디피아이 | 우레탄 변성 폴리에스테르 수지 조성물, 이의 제조 방법및 이를 포함하는 도료 조성물 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57112410A (en) * | 1980-12-27 | 1982-07-13 | Toho Rayon Co Ltd | Acrylonitrile fiber and its production |
| DD287742A5 (de) * | 1989-09-08 | 1991-03-07 | Veb Fettchemie,De | Verfahren zur erzielung eines gegen hydrothermische einfluesse stabilen avivageeffektes auf polyacrylnitrilfaserstoffen |
| EP0507973A1 (de) * | 1991-04-10 | 1992-10-14 | FRATELLI LAMBERTI S.p.A. | Biologisch abbaubare Zusammensetzungen, ihre Verwendung als Textilweichmacher |
-
1992
- 1992-07-03 IT ITMI921625A patent/IT1255205B/it active IP Right Grant
-
1993
- 1993-06-11 EP EP9393109508A patent/EP0576896A3/de not_active Withdrawn
- 1993-06-30 JP JP5160959A patent/JPH06166959A/ja active Pending
- 1993-07-02 KR KR1019930012357A patent/KR940002422A/ko not_active Withdrawn
- 1993-07-02 MY MYPI93001302A patent/MY131451A/en unknown
- 1993-07-03 CN CN93107927A patent/CN1083880A/zh active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5403426A (en) * | 1991-05-28 | 1995-04-04 | Hercules Incorporated | Process of making cardable hydrophobic polypropylene fiber |
| US5958806A (en) * | 1994-01-14 | 1999-09-28 | Fibervisions A/S | Cardable hydrophobic polyolefin fibres comprising cationic spin finishes |
| US8092723B2 (en) | 2005-11-18 | 2012-01-10 | Nanocomp Oy Ltd | Method of producing a diffraction grating element |
| WO2009129364A3 (en) * | 2008-04-17 | 2009-12-10 | The Dow Chemical Company | Durable functionalization of polyolefin fibers and fabrics for moisture management and odor control |
Also Published As
| Publication number | Publication date |
|---|---|
| ITMI921625A0 (it) | 1992-07-03 |
| JPH06166959A (ja) | 1994-06-14 |
| EP0576896A3 (de) | 1994-10-19 |
| ITMI921625A1 (it) | 1994-01-03 |
| CN1083880A (zh) | 1994-03-16 |
| MY131451A (en) | 2007-08-30 |
| IT1255205B (it) | 1995-10-20 |
| KR940002422A (ko) | 1994-02-17 |
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| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
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| RHK1 | Main classification (correction) |
Ipc: D06M 13/402 |
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| 17P | Request for examination filed |
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| 17Q | First examination report despatched |
Effective date: 19950802 |
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| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
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| 18D | Application deemed to be withdrawn |
Effective date: 19960213 |