EP2169110A1 - Fire-resistant hollow fibres with silicon-free soft grip apparatus - Google Patents
Fire-resistant hollow fibres with silicon-free soft grip apparatus Download PDFInfo
- Publication number
- EP2169110A1 EP2169110A1 EP20080016820 EP08016820A EP2169110A1 EP 2169110 A1 EP2169110 A1 EP 2169110A1 EP 20080016820 EP20080016820 EP 20080016820 EP 08016820 A EP08016820 A EP 08016820A EP 2169110 A1 EP2169110 A1 EP 2169110A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- retardant modified
- flame
- fiber according
- modified fiber
- fibers
- 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
- 230000009970 fire resistant effect Effects 0.000 title 1
- 239000000835 fiber Substances 0.000 claims abstract description 101
- 229920000642 polymer Polymers 0.000 claims abstract description 11
- 239000004753 textile Substances 0.000 claims abstract description 8
- 239000000945 filler Substances 0.000 claims abstract description 7
- 239000003063 flame retardant Substances 0.000 claims description 47
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 46
- 229920000728 polyester Polymers 0.000 claims description 33
- -1 aromatic dicarboxylic acids Chemical class 0.000 claims description 19
- 229920000570 polyether Polymers 0.000 claims description 18
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 16
- 239000000194 fatty acid Substances 0.000 claims description 16
- 229930195729 fatty acid Natural products 0.000 claims description 16
- 239000007859 condensation product Substances 0.000 claims description 14
- 239000012510 hollow fiber Substances 0.000 claims description 14
- 150000004665 fatty acids Chemical class 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 125000003118 aryl group Chemical group 0.000 claims description 9
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 6
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 125000001142 dicarboxylic acid group Chemical group 0.000 claims description 5
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 5
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 5
- 239000002202 Polyethylene glycol Substances 0.000 claims description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 4
- 239000004744 fabric Substances 0.000 claims description 4
- 125000001072 heteroaryl group Chemical group 0.000 claims description 4
- 229920001223 polyethylene glycol Polymers 0.000 claims description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 4
- 238000007792 addition Methods 0.000 claims description 3
- 238000000429 assembly Methods 0.000 claims description 3
- 230000000712 assembly Effects 0.000 claims description 3
- 150000002009 diols Chemical group 0.000 claims description 3
- 125000003827 glycol group Chemical group 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical class [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- 235000011037 adipic acid Nutrition 0.000 claims description 2
- 239000001361 adipic acid Substances 0.000 claims description 2
- 150000001298 alcohols Chemical class 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 150000002366 halogen compounds Chemical class 0.000 claims description 2
- 150000003018 phosphorus compounds Chemical class 0.000 claims description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 2
- 238000009833 condensation Methods 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 239000011810 insulating material Substances 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 4
- 238000002788 crimping Methods 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000007796 conventional method Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000009987 spinning Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- FMFKNGWZEQOWNK-UHFFFAOYSA-N 1-butoxypropan-2-yl 2-(2,4,5-trichlorophenoxy)propanoate Chemical compound CCCCOCC(C)OC(=O)C(C)OC1=CC(Cl)=C(Cl)C=C1Cl FMFKNGWZEQOWNK-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229910010413 TiO 2 Inorganic materials 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- JXTHNDFMNIQAHM-UHFFFAOYSA-N dichloroacetic acid Chemical compound OC(=O)C(Cl)Cl JXTHNDFMNIQAHM-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229920004935 Trevira® Polymers 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000012867 bioactive agent Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229960005215 dichloroacetic acid Drugs 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000007380 fibre production Methods 0.000 description 1
- 239000012765 fibrous filler Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 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
-
- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47G—HOUSEHOLD OR TABLE EQUIPMENT
- A47G9/00—Bed-covers; Counterpanes; Travelling rugs; Sleeping rugs; Sleeping bags; Pillows
- A47G9/02—Bed linen; Blankets; Counterpanes
- A47G9/0207—Blankets; Duvets
-
- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47G—HOUSEHOLD OR TABLE EQUIPMENT
- A47G9/00—Bed-covers; Counterpanes; Travelling rugs; Sleeping rugs; Sleeping bags; Pillows
- A47G9/10—Pillows
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B68—SADDLERY; UPHOLSTERY
- B68G—METHODS, EQUIPMENT, OR MACHINES FOR USE IN UPHOLSTERING; UPHOLSTERY NOT OTHERWISE PROVIDED FOR
- B68G1/00—Loose filling materials for upholstery
-
- 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
- D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
-
- 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
- D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
- D06M13/2243—Mono-, di-, or triglycerides
-
- 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
- D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
- D06M13/2246—Esters of unsaturated carboxylic acids
-
- 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
-
- 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
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/53—Polyethers
-
- 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
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/16—Synthetic fibres, other than mineral fibres
- D06M2101/30—Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M2101/32—Polyesters
-
- 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
- Y10T428/23—Sheet including cover or casing
- Y10T428/237—Noninterengaged fibered material encased [e.g., mat, batt, etc.]
-
- 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
- Y10T428/249921—Web or sheet containing structurally defined element or component
-
- 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
- Y10T428/2922—Nonlinear [e.g., crimped, coiled, etc.]
- Y10T428/2924—Composite
-
- 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
- Y10T428/2935—Discontinuous or tubular or cellular core
Definitions
- the invention relates to a flame-retardant modified hollow fiber with a silicone-free soft-grip equipment, and a method for producing the same and their use for Mountainmaschine effort.
- Fiber fillings can be used in many applications, such as apparel, cushions, furniture, insulation, quilts, filters, upholstery (e.g., in cars), sleeping bags, mattress pads, and mattresses.
- the hollow fibers used for these applications are generally hollow fibers which are flame-retardant with phosphorus-containing compounds.
- polyester hollow fibers are preferably used.
- fiber fillings are provided with a so-called softening finish with a pleasant feel, improved fluffiness, improved surface smoothness, and improved recovery.
- silicone-based softening is used, such as, for example, in US Pat WO 2004/007 347 (Trevira GmbH), US 3,271,189 (Hofmann ) and in U.S. 3,454,422 (Mead et al. ) disclosed.
- the object of the present invention is therefore to provide flame-retardant hollow fibers with a soft-grip finish which does not impair the flame-retardant properties of the hollow fibers.
- the present invention therefore provides flame-retardant modified fibers based on melt-spinnable polymers, in particular based on polyesters, characterized in that these fibers are provided with a soft-grip finish which is silicone-free.
- the fibers of melt-spinnable polymers according to the invention are preferably fibers based on polyesters.
- Suitable polyester materials are in principle all known types suitable for fiber production.
- Such polyesters consist predominantly of building blocks derived from aromatic dicarboxylic acids and from aliphatic diols.
- Common aromatic dicarboxylic acid building blocks are the divalent radicals of benzenedicarboxylic acids, in particular terephthalic acid and isophthalic acid.
- Common diols have 2 to 4 carbon atoms, with the ethylene glycol being particularly suitable.
- Particularly advantageous are fibers which consist of at least 85 mol% of polyethylene terephthalate.
- the remaining 15 mol% are made up of dicarboxylic acid units and glycol units which act as so-called modifying agents and which allow the person skilled in the art to influence the physical and chemical properties of the filaments produced in a targeted manner.
- dicarboxylic acid units are residues of isophthalic acid or of aliphatic dicarboxylic acids, such as glutaric acid, adipic acid and sebacic acid.
- modifying diol radicals are those of longer-chain diols, for example of propanediol or butanediol, of di- or triethylene glycol, or, if present in a small amount, of polyglycol having a molecular weight of about 500 to 2,000.
- Particularly preferred are polyesters containing at least 95 mol% of polyethylene terephthalate (PET), in particular PET not modified with dicarboxylic acid units and / or glycol units.
- PET polyethylene terephthalate
- the flame retardant modification of the polyester fibers is achieved by using flame retardant modified polyesters.
- flame-retardant modified polyesters are known. They contain additions of halogen compounds, in particular bromine compounds, or, what is particularly advantageous, they contain phosphorus compounds which are condensed in the polyester chain.
- these condensed-in phosphorus-containing chain links are understood to be chain links which are arranged in the linear chain of the polymer molecule (longest chain), but also in any side chains and branches that may be present.
- flame-retardant modified polyesters which contain condensed in the chain assemblies of the formula (I) wherein R is alkylene or polymethylene having 2 to 6 carbon atoms or phenyl and R 1 is alkyl having 1 to 6 carbon atoms, aryl or aralkyl.
- R is ethylene and R 1 is methyl, ethyl, phenyl, or o-, m- or p-methylphenyl, in particular methyl.
- Such polyesters are, for example, in the DE-A-39 40 713 described.
- the polyesters used in the invention preferably have a molecular weight corresponding to an intrinsic viscosity (IV), measured in a solution of 1 g of polymer in 100 ml of dichloroacetic acid at 25 ° C, from 0.45 to 0.85.
- IV intrinsic viscosity
- the silicone-free softener finish of the present invention is a blend comprising at least one polyether and at least one Fatty acid condensation product.
- this mixture preferably has a mixing ratio (weight) of polyether: fatty acid condensation product of 10: 1 to 1: 1, in particular of 5: 1 to 2: 1, particularly preferably of 4: 1.
- R 2 are straight-chain or branched alkyl groups, in particular ethyl (polyethylene glycol) or propyl groups (propylene glycol).
- the end groups R 3 , R 4 are usually hydrogen, but may also be substituted by the same groups as mentioned above for R 3 , R 4 .
- Preferred compounds of the formula (II) are nonionic polyethers. It is further preferred if the polyethers are miscible with water and have a pH in the range from 6 to 9, in particular from 7 to 8, particularly preferably from 7.5 as 10% solution (weight percent). It is further preferred if the dynamic viscosity of the polyethers (measured as 10% strength solution in water) at 20 ° C. (HTC51) is preferably between 50 and 80 mPas, in particular between 60 and 70 mPas, particularly preferred at 65 mPas ,
- Such polyethers are commercially available, for example under the trade name Duron® FF 1751, a product of CHT R. Beitlich GmbH.
- Fatty acid condensation products of the invention suitable for softening equipment are compounds of fatty acids having the general formula R 5 -COOH, where R 5 denotes straight-chain or branched, alkyl or alkenyl groups having 6 to 30 carbon atoms, preferably 6 to 26 carbon atoms, with aliphatic or aromatic, mono- or polyfunctional alcohols or amines.
- Preferred fatty acid condensation products according to the invention are fatty acid condensation products, in particular cationic fatty acid condensation products, which are completely miscible with water and have a pH in the range from 1 to 6, preferably 2 to 5, particularly preferably 3, as the 10% solution (weight percent) to 4, have.
- Their dynamic viscosity (measured as 10% by weight solution in water) at 20 ° C. is preferably between 80 and 120 mPas, preferably between 90 and 110 mPas, particularly preferably about 100 mPas.
- Duron® FF 1995 a product of CHT R. Beitlich GmbH.
- a softening finish comprising (i) non-ionic polyethers whose pH (measured as 10% strength by weight solution in water at 20 ° C.) is between 7 and 8 and whose dynamic viscosity of the polyethers (measured as 10 wt .-% - solution in water at 20 ° C) is between 50 and 80 mPas and (ii) cationic fatty acid condensation products whose pH (measured as 10 wt .-% solution in water at 20 ° C) in the range of 2 to 5 and their dynamic viscosity (measured as 10% by weight solution in water) at 20 ° C between 80 and 120 mPas and wherein the mixing ratio (parts by weight) of nonionic polyether (i) to cationic fatty acid condensation product (ii) is 5: 1 to 2: 1.
- Silicone-free means that silicon-containing material is contained as little as possible so that the flame retardant properties according to the invention are not impaired. This is the case for amounts of no more than about 10 ppm of silicone-containing material relative to the finished hollow fiber, preferably less than about 1 ppm, more preferably less than about 0.1 ppm.
- the fibers may have round, oval and other suitable cross-sections or other shapes, such as dumbbell, kidney-shaped, triangular or trilobal or multilobal cross-sections. Hollow fibers are preferably used.
- Polyester fibers generally have titer values in the range of 0.9 to 16 dtex. Polyester hollow fibers having the above values are preferably used, preferably with titres of 0.9 to 17 dtex, more preferably 4 to 13 dtex. If the polyester hollow fibers according to the invention are to be used as staple fibers, they have a cut length (staple length) of 1 to 150 mm, preferably 8 to 100 mm and particularly preferably 24 to 80 mm.
- the polyester fibers consist of a Titer mixture and / or a mixture of fibers with different staple length.
- polyester fibers according to the invention are used for textile applications or as filler fiber packing, texturing is advantageous, in particular crimping.
- the degree of crimping is 2 crimps (crimps) per cm (Bg) or more, preferably 3 sheets per cm or more.
- the number of sheets per cm must also be in a certain ratio to the so-called crimp K1.
- K1 preferably has values of at least 15%, preferably at least 18%. Accordingly, the ratio of curling to number of sheets per cm is preferably in the range of 5 ⁇ K1 / Bg ⁇ 6 at a number of sheets per cm Bg of 3.0.
- the stretching is carried out using the so-called Entk Hurselungskraft. This is determined in preliminary tests by means of a tangent applied to the force-strain diagram of the respective fiber.
- the flame retardant fibers of the invention may additionally comprise other additives commonly used in the art. These include in particular antioxidants, stabilizers (eg UV stabilizers), matting agents (eg TiO 2 zinc sulfide or zinc oxide), pigments (eg TiO 2 ), additional flame retardants, antistatic agents, dyes, fillers (eg calcium carbonate), antimicrobial agents, bioactive agents, optical Brighteners, extenders and other processing aids to understand.
- additives commonly used in the art. These include in particular antioxidants, stabilizers (eg UV stabilizers), matting agents (eg TiO 2 zinc sulfide or zinc oxide), pigments (eg TiO 2 ), additional flame retardants, antistatic agents, dyes, fillers (eg calcium carbonate), antimicrobial agents, bioactive agents, optical Brighteners, extenders and other processing aids to understand.
- Such additives may be added to the polymer at any time during polymer preparation or applied to the fibers with the finish.
- Fiber fabrication is accomplished by spinning polymers into filaments, optionally with lubricants, and then processing into fibers, drawing and crimping the fibers, and optionally applying an antistatic agent to the fibers.
- the fibers are cut and then pressed into so-called flake bales and packaged.
- Fabrication of the fibers is accomplished using conventional methods and equipment as are preferred in the art in the context of polyester fibers. For example, numerous methods of spinning in US 3,816,486 . U.S. 4,639,347 . GB 1 254 826 and JP 11-189938 described.
- the spinning speed is preferably 800 meters per minute or more, and is typically 1600 meters per minute or less.
- the spinning temperature is typically 255 ° C or more and 305 ° C or less. More preferably, spinning is carried out at about 280 ° C.
- the spinneret is a conventional spinneret of the type used in conventional polyesters, with hole size, location and number depending on the desired fiber and spin line.
- Quenching of the melt-spun polyester filaments in this manner may be carried out in a conventional manner using air or other fluids as described in the art (e.g., nitrogen). Cross-flow, radial, asymmetric or other cooling methods can be used. It is preferred to blow with air for quenching.
- air or other fluids as described in the art (e.g., nitrogen).
- Cross-flow, radial, asymmetric or other cooling methods can be used. It is preferred to blow with air for quenching.
- the fiber filaments thus produced are first deposited in cans for further processing.
- the melt-spun fiber filaments are taken up on a spinning-cable cylinder and subsequently a plurality of spinning-wire cylinders are assembled and a large tow is produced from the fiber-filaments.
- the fiber tows can be drawn using conventional techniques, preferably at 10 to 110 m / min.
- the draw ratios are preferably from 1.25 to 4, more preferably from 2.5 to 3.5, most preferably 3.2.
- the temperature during the drawing is in the range of the glass transition temperature of the polyester cable to be stretched and is preferably 40 ° C. to 80 ° C. and is particularly preferably 69 ° C.
- the aftertreatment is carried out at about 150 ° to 165 ° C to ensure good drying.
- the stretching can be carried out optionally using a two-stage stretching process (see, for example, the US 3,816,486 ). Before and during drawing, one or more finishes may be applied using conventional techniques.
- the silicone-free soft-grip equipment according to the invention is applied between the stretching and the crimping.
- the application is carried out by conventional techniques, in particular by spraying or by means of an applicator roll.
- the amount applied is between 0.4 and 0.5% of the fiber weight and is preferably 0.46%.
- crimping machines For the crimping of the fibers thus stretched, conventional methods of mechanical crimping can be used with known crimping machines. Preferred is a mechanical device for staple fiber crimping with steam assist, such as a stuffer box. However, crimped fibers can also be used according to other methods, for example also three-dimensionally crimped fibers.
- the cable is first heated to a temperature in the range of 60 ° to 100 ° C., preferably 70 ° to 85 ° C., particularly preferably about 83 ° C., and with a pressure of the cable entry rollers of 1.0 to 2, 0 bar, more preferably at about 1.5 bar, a pressure in the crimping chamber of 0.5 to 1.0 bar, particularly preferably 0.8 bar, with steam at between 1.0 and 2.0 kg / min., especially preferably 1.5 kg / min, treated.
- the fibers are relaxed at 150 ° to 165 ° C in the oven and / or fixed.
- the preparation does not need its own fixation step.
- antistatic finish may be applied to the fibers after relaxation.
- the fibers can be made pillar free.
- the textured fibers are taken up, followed by cutting and possibly hardening and depositing in pressed bales as a flake.
- the staple fibers of the present invention are preferably cut on a relaxation downstream mechanical cutter.
- For the production of cable types can be dispensed with the cutting. These cable types are placed in uncut form in the bale and pressed.
- Another object is the use of the fiber products according to the invention as fiber fillers or in textile fabrics.
- fibrous fillers includes fillings for filled covers, e.g. Pillows, duvets, quilts and the like, as well as for mattresses and sleeping bags, insulation and upholstery, for example for furniture and in the automotive sector, as well as filters.
- Inventive textile fabrics are, for example, clothing, the upper and lower webs of the above-mentioned covers, as well as mattress pads.
- a staple fiber with a hollow profile is spun from the melt in the usual way for fibers from the flame-retardant raw material, cooled by blowing with air, provided with conventional staple fiber preparation and stored in cans for processing on the strip line.
- the spun goods are collected as a fiber cable via an inlet rake and fed by a first septet, consisting of seven rotating rollers, passed through a dip bath, where it is tempered and again provided with preparation.
- the spun goods are transported by another septet.
- the stretching takes place on the sixth or seventh roll of this septet or between this and a further septet running faster by the factor of stretching.
- the fiber is crimped in a stuffer box, fixed in the oven or dried and optionally cut. Between drawing and crimping, the addition of a silicone-free softening equipment by spraying or by application roller.
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Abstract
Description
Die Erfindung betrifft eine flammhemmend modifizierte Hohlfaser mit einer silikonfreien Weichgriffausrüstung, sowie ein Verfahren zur Herstellung derselben und deren Verwendung für Füllfaserprodukte.The invention relates to a flame-retardant modified hollow fiber with a silicone-free soft-grip equipment, and a method for producing the same and their use for Füllfaserprodukte.
Faserfüllungen können in vielen Anwendungen eingesetzt werden, beispielsweise für Bekleidung, Kissen, Möbel, Dämmung, Steppdecken, Filter, Polsterungen (z.B. in Autos), Schlafsäcke, Matratzenauflagen und Matratzen. Bei den für diese Anwendungen verwendeten Hohlfasern handelt es sich im Allgemeinen um Hohlfasern, die mit phosphorhaltigen Verbindungen flammhemmend ausgerüstet sind. Als Hohlfasern werden bevorzugt Polyesterhohlfasern verwendet.Fiber fillings can be used in many applications, such as apparel, cushions, furniture, insulation, quilts, filters, upholstery (e.g., in cars), sleeping bags, mattress pads, and mattresses. The hollow fibers used for these applications are generally hollow fibers which are flame-retardant with phosphorus-containing compounds. As hollow fibers polyester hollow fibers are preferably used.
Die Herstellung entsprechender flammhemmend modifizierter Polyesterfasern, bei denen der Polyester mitkondensierte phosphorhaltige Kettenglieder aufweist, ist an sich bekannt. Es wird an dieser Stelle auf die deutschen Patentanmeldungen bzw. Patentschriften
Die dort beschriebenen Fasern wurden bisher als solche lediglich dort eingesetzt, wo es auf die Flammhemmung ankommt.The fibers described there were previously used as such only where it depends on the flame retardancy.
Weiterhin werden Faserfüllungen durch eine sogenannte Weichgriffausrüstung mit einem angenehmen Griff, verbesserter Flauschigkeit, verbesserter Oberflächenglätte und verbessertem Wiedererholungsvermögen ausgestattet. Für diese Weichgriffausrüstung wird gemäß Stand der Technik eine Avivage auf Silikonbasis verwendet, wie z.B. in
Allerdings ist von solchen Fasern mit einer silikonhaltigen Weichgriffausrüstung bekannt, dass durch diese silikonhaltige Weichgriffausrüstung die flammhemmenden Eigenschaften sehr stark beeinträchtigt werden.However, it is known of such fibers with a silicone-containing softening finish that this silicone-containing softening finish severely impairs the flame retardant properties.
Aufgabe der vorliegenden Erfindung ist daher, flammhemmende Hohlfasern mit einer Weichgriffausrüstung auszustatten, welche die flammhemmenden Eigenschaften der Hohlfasern nicht beeinträchtigt.The object of the present invention is therefore to provide flame-retardant hollow fibers with a soft-grip finish which does not impair the flame-retardant properties of the hollow fibers.
Es wurde gefunden, dass bei flammhemmend ausgerüsteten Polyesterhohlfasern, die mit der erfindungsgemäßen silikonfreien Weichgriffausrüstung versehen werden, einerseits die flammhemmenden Eigenschaften der Hohlfasern nicht durch die aufgebrachte Weichgriffausrüstung beeinträchtigt wird und andererseits der gewünschte Weichgriff erhalten wird.It has been found that in flame-retardant polyester hollow fibers provided with the silicone-free softening finish according to the invention, on the one hand, the flame-retardant properties of the hollow fibers are not impaired by the applied soft-grip finish and, on the other hand, the desired softening is obtained.
Gegenstand der vorliegenden Erfindung sind daher flammhemmend modifizierte Fasern auf der Basis von schmelzspinnbaren Polymeren, insbesondere auf der Basis von Polyestern, dadurch gekennzeichnet, dass diese Fasern mit einer Weichgriffausrüstung versehen sind, die silikonfrei ist.The present invention therefore provides flame-retardant modified fibers based on melt-spinnable polymers, in particular based on polyesters, characterized in that these fibers are provided with a soft-grip finish which is silicone-free.
Bei den erfindungsgemäßen Fasern aus schmelzspinnbaren Polymeren handelt es sich bevorzugt um Fasern auf der Basis von Polyestern. Als Polyestermaterial kommen im Prinzip alle zur Faserherstellung geeigneten bekannten Typen in Betracht. Derartige Polyester bestehen überwiegend aus Bausteinen, die sich von aromatischen Dicarbonsäuren und von aliphatischen Diolen ableiten. Gängige aromatische Dicarbonsäurebausteine sind die zweiwertigen Reste von Benzoldicarbonsäuren, insbesondere der Terephthalsäure und der Isophthalsäure. Gängige Diole haben 2 bis 4 Kohlenstoffatome, wobei das Ethylenglykol besonders geeignet ist. Besonders vorteilhaft sind Fasern, die zu mindestens 85 mol-% aus Polyethylenterephthalat bestehen. Die restlichen 15 mol-% bauen sich aus Dicarbonsäureeinheiten und Glykoleinheiten auf, die als sogenannte Modifizierungsmittel wirken und die es dem Fachmann gestatten, die physikalischen und chemischen Eigenschaften der hergestellten Filamente gezielt zu beeinflussen. Beispiele für solche Dicarbonsäureeinheiten sind Reste der Isophthalsäure oder von aliphatischen Dicarbonsäuren, wie Glutarsäure, Adipinsäure und Sebacinsäure. Beispiele für modifizierend wirkende Diolreste sind solche von längerkettigen Diolen, z.B. von Propandiol oder Butandiol, von Di- oder Triethylenglykol, oder, sofern in geringer Menge vorhanden, von Polyglykol mit einem Molekulargewicht von ca. 500 bis 2000. Besonders bevorzugt sind Polyester, die mindestens 95 mol-% Polyethylenterephthalat (PET) enthalten, insbesondere nicht mit Dicarbonsäureeinheiten und/oder Glykoleinheiten modifiziertes PET.The fibers of melt-spinnable polymers according to the invention are preferably fibers based on polyesters. Suitable polyester materials are in principle all known types suitable for fiber production. Such polyesters consist predominantly of building blocks derived from aromatic dicarboxylic acids and from aliphatic diols. Common aromatic dicarboxylic acid building blocks are the divalent radicals of benzenedicarboxylic acids, in particular terephthalic acid and isophthalic acid. Common diols have 2 to 4 carbon atoms, with the ethylene glycol being particularly suitable. Particularly advantageous are fibers which consist of at least 85 mol% of polyethylene terephthalate. The remaining 15 mol% are made up of dicarboxylic acid units and glycol units which act as so-called modifying agents and which allow the person skilled in the art to influence the physical and chemical properties of the filaments produced in a targeted manner. Examples of such dicarboxylic acid units are residues of isophthalic acid or of aliphatic dicarboxylic acids, such as glutaric acid, adipic acid and sebacic acid. Examples of modifying diol radicals are those of longer-chain diols, for example of propanediol or butanediol, of di- or triethylene glycol, or, if present in a small amount, of polyglycol having a molecular weight of about 500 to 2,000. Particularly preferred are polyesters containing at least 95 mol% of polyethylene terephthalate (PET), in particular PET not modified with dicarboxylic acid units and / or glycol units.
Die flammhemmende Modifizierung der Polyesterfasern wird durch Verwendung von flammhemmend modifizierten Polyestern erzielt. Derartige flammhemmend modifizierte Polyester sind bekannt. Sie enthalten Zusätze von Halogenverbindungen, insbesondere Bromverbindungen, oder, was besonders vorteilhaft ist, sie enthalten Phosphorverbindungen, die in der Polyesterkette einkondensiert sind.The flame retardant modification of the polyester fibers is achieved by using flame retardant modified polyesters. Such flame-retardant modified polyesters are known. They contain additions of halogen compounds, in particular bromine compounds, or, what is particularly advantageous, they contain phosphorus compounds which are condensed in the polyester chain.
Unter diesen einkondensierten phosphorhaltigen Kettengliedern im Sinne der Erfindung sind Kettenglieder zu verstehen, die in der linearen Kette des Polymermoleküls (längste Kette), aber auch in ggf. vorhandenen Seitenketten und Verzweigungen angeordnet sind.For the purposes of the invention, these condensed-in phosphorus-containing chain links are understood to be chain links which are arranged in the linear chain of the polymer molecule (longest chain), but also in any side chains and branches that may be present.
Besonders bevorzugt sind flammhemmend modifizierte Polyester, die in der Kette Baugruppen der Formel (I) einkondensiert enthalten
Bei der erfindungsgemäßen silikonfreien Weichgriffausrüstung handelt es sich um eine Mischung, umfassend mindestens einen Polyether und mindestens ein Fettsäurekondensationsprodukt. Diese Mischung weist erfindungsgemäß bevorzugt ein Mischungsverhältnis (Gewicht) von Polyether:Fettsäurekondensationsprodukt von 10:1 bis 1:1 1 auf, insbesondere von 5:1 bis 2:1, besonders bevorzugt von 4:1.The silicone-free softener finish of the present invention is a blend comprising at least one polyether and at least one Fatty acid condensation product. According to the invention, this mixture preferably has a mixing ratio (weight) of polyether: fatty acid condensation product of 10: 1 to 1: 1, in particular of 5: 1 to 2: 1, particularly preferably of 4: 1.
Für die erfindungsgemäße Weichgriffausrüstung geeignete Polyether sind Verbindungen mit der allgemeinen Formel
- R3, R4 gleich oder verschieden sein können und ausgewählt werden aus Wasserstoff, geradkettigen und/oder verzweigten Alkyl- und /oder Alkenylgruppen, sowie aromatischen und/oder heteroaromatischen Gruppen,
- R2 gleich oder verschieden sein können und ausgewählt werden aus geradkettigen und/oder verzweigten Alkyl- und /oder Alkenylgruppen, sowie aromatischen und/oder heteroaromatischen Gruppen und
- n eine Zahl von mindestens 1, vorzugsweise mindestens 2, bedeuten.
- R 3 , R 4 may be identical or different and are selected from hydrogen, straight-chain and / or branched alkyl and / or alkenyl groups, and also aromatic and / or heteroaromatic groups,
- R 2 may be the same or different and are selected from straight-chain and / or branched alkyl and / or alkenyl groups, as well as aromatic and / or heteroaromatic groups and
- n is a number of at least 1, preferably at least 2.
Bevorzugte Reste R2 sind geradkettige oder verzweigte Alkylgruppen, insbesondere Ethyl-(Polyethylenglykol) oder Propylgruppen (Propylenglykol). Die Endgruppen R3, R4 sind meist Wasserstoff, können aber auch mit den gleichen Gruppen wie oben für R3, R4 genannt, substituiert sein.Preferred radicals R 2 are straight-chain or branched alkyl groups, in particular ethyl (polyethylene glycol) or propyl groups (propylene glycol). The end groups R 3 , R 4 are usually hydrogen, but may also be substituted by the same groups as mentioned above for R 3 , R 4 .
Bevorzugte Verbindungen der Formel (II) sind nichtionogene Polyether. Weiter bevorzugt ist, wenn die Polyether mit Wasser mischbar sind und als 10%-ige Lösung (Gewichtsprozent) einen pH-Wert im Bereich von 6 bis 9, insbesondere von 7 bis 8, besonders bevorzugt von 7,5 aufweisen. Weiterhin bevorzugt ist es, wenn die dynamische Viskosität der Polyether (gemessen als 10%-ige Lösung in Wasser) bei 20°C (HTC51) vorzugsweise zwischen 50 und 80 mPas, insbesondere zwischen 60 und 70 mPas, besonders bevorzugt bei 65 mPas, beträgt.Preferred compounds of the formula (II) are nonionic polyethers. It is further preferred if the polyethers are miscible with water and have a pH in the range from 6 to 9, in particular from 7 to 8, particularly preferably from 7.5 as 10% solution (weight percent). It is further preferred if the dynamic viscosity of the polyethers (measured as 10% strength solution in water) at 20 ° C. (HTC51) is preferably between 50 and 80 mPas, in particular between 60 and 70 mPas, particularly preferred at 65 mPas ,
Derartige Polyether sind im Handel erhältlich, beispielsweise unter der Handelsbezeichnung Duron® FF 1751, einem Produkt der Firma CHT R. Beitlich GmbH.Such polyethers are commercially available, for example under the trade name Duron® FF 1751, a product of CHT R. Beitlich GmbH.
Erfindungsgemäße, für die Weichgriffausrüstung geeignete Fettsäurekondensationsprodukte sind Verbindungen aus Fettsäuren mit der allgemeinen Formel
R5-COOH,
wobei R5 geradkettige oder verzweigte, Alkyl- oder Alkenylgruppen mit 6 bis 30 Kohlenstoffatomen, bevorzugt 6 bis 26 Kohlenstoffatomen, bezeichnet,
mit aliphatischen oder aromatischen, einfach oder mehrfach funktionellen Alkoholen oder Aminen.Fatty acid condensation products of the invention suitable for softening equipment are compounds of fatty acids having the general formula
R 5 -COOH,
where R 5 denotes straight-chain or branched, alkyl or alkenyl groups having 6 to 30 carbon atoms, preferably 6 to 26 carbon atoms,
with aliphatic or aromatic, mono- or polyfunctional alcohols or amines.
Unter diesen oben genannten Fettsäurekondensationsprodukten sind erfindungsgemäß Fettsäurekondensationsprodukt, insbesondere kationische Fettsäurekondensationsprodukte, bevorzugt, die mit Wasser vollständig mischbar sind und als 10%-ige Lösung (Gewichtsprozent) einen pH-Wert im Bereich von 1 bis 6, bevorzugt 2 bis 5, besonders bevorzugt 3 bis 4 ,aufweisen. Ihre dynamische Viskosität (gemessen als 10Gew.-%-ige Lösung in Wasser) bei 20°C beträgt vorzugsweise zwischen 80 und 120 mPas, bevorzugt zwischen 90 und 110 mPas, besonders bevorzugt bei etwa 100 mPas.Preferred fatty acid condensation products according to the invention are fatty acid condensation products, in particular cationic fatty acid condensation products, which are completely miscible with water and have a pH in the range from 1 to 6, preferably 2 to 5, particularly preferably 3, as the 10% solution (weight percent) to 4, have. Their dynamic viscosity (measured as 10% by weight solution in water) at 20 ° C. is preferably between 80 and 120 mPas, preferably between 90 and 110 mPas, particularly preferably about 100 mPas.
Ein solches im Handel erhältliches Fettsäurekondensationsprodukt ist Duron® FF 1995, ein Produkt der Firma CHT R. Beitlich GmbH.One such commercially available fatty acid condensation product is Duron® FF 1995, a product of CHT R. Beitlich GmbH.
Besonders bevorzugt ist eine Weichgriffausrüstung umfassend (i) nichtionogene Polyether, deren pH-Wert (gemessen als 10 Gew.-%-ige Lösung in Wasser bei 20°C) zwischen 7 und 8 beträgt und dessen dynamische Viskosität der Polyether (gemessen als 10 Gew.-%-ige Lösung in Wasser bei 20°C) zwischen 50 und 80 mPas beträgt und (ii) kationische Fettsäurekondensationsprodukte deren pH-Wert (gemessen als 10 Gew.-%-ige Lösung in Wasser bei 20°C) im Bereich von 2 bis 5 liegt und deren dynamische Viskosität (gemessen als 10Gew.-%-ige Lösung in Wasser) bei 20°C zwischen 80 und 120 mPas beträgt und wobei der das Mischungsverhältnis (Gewichtsteile) von nichtionogenem Polyether (i) zu kationischem Fettsäurekondensationsprodukt (ii) 5:1 bis 2:1 beträgt.Particularly preferred is a softening finish comprising (i) non-ionic polyethers whose pH (measured as 10% strength by weight solution in water at 20 ° C.) is between 7 and 8 and whose dynamic viscosity of the polyethers (measured as 10 wt .-% - solution in water at 20 ° C) is between 50 and 80 mPas and (ii) cationic fatty acid condensation products whose pH (measured as 10 wt .-% solution in water at 20 ° C) in the range of 2 to 5 and their dynamic viscosity (measured as 10% by weight solution in water) at 20 ° C between 80 and 120 mPas and wherein the mixing ratio (parts by weight) of nonionic polyether (i) to cationic fatty acid condensation product (ii) is 5: 1 to 2: 1.
Ganz besonders bevorzugt handelt es sich bei dem vorstehend genannten Gemisch aus (i) nichtionogenem Polyether und (ii) kationischem Fettsäurekondensationsprodukt um solche, bei denen die Polyether (i) verschiedene Polyether, ausgewählt aus der Gruppe Polyethylenglykol, Polypropylenglykol oder Mischungen aus Polyethylenglykol und Polypropylenglykol, umfassen.Very particular preference is given to the abovementioned mixture of (i) nonionic polyether and (ii) cationic fatty acid condensation product to those in which the polyethers (i) are different polyethers selected from the group of polyethylene glycol, polypropylene glycol or mixtures of polyethylene glycol and polypropylene glycol, include.
Mit dem erfindungsgemäßen Einsatz dieser silikonfreien Weichgriffausrüstung auf den flammhemmenden Fasern ist es möglich, Faserprodukte, insbesondere für den Füllfaserbereich herzustellen, die sowohl über Weichgriff als auch über flammhemmende Eigenschaften verfügen.With the use according to the invention of this silicone-free soft-grip finish on the flame-retardant fibers, it is possible to produce fiber products, in particular for the filling fiber sector, which have both soft feel and flame-retardant properties.
Unter silikonfrei versteht man dabei, dass sowenig silikonhaltiges Material enthalten ist, dass die erfindungsgemäßen flammhemmenden Eigenschaften nicht beeinträchtigt werden. Dies ist bei Mengen von maximal etwa 10 ppm silikonhaltigem Material in Bezug auf die ausgerüstete Hohlfaser der Fall, bevorzugt weniger als etwa 1 ppm, besonders bevorzugt weniger als etwa 0,1 ppm.Silicone-free means that silicon-containing material is contained as little as possible so that the flame retardant properties according to the invention are not impaired. This is the case for amounts of no more than about 10 ppm of silicone-containing material relative to the finished hollow fiber, preferably less than about 1 ppm, more preferably less than about 0.1 ppm.
Die Fasern können runde, ovale und weitere geeignete Querschnitte oder auch andere Formen aufweisen, wie zum Beispiel hantel-, nierenförmige, dreieckige bzw. tri- oder multilobale Querschnitte. Bevorzugt werden Hohlfasern eingesetzt.The fibers may have round, oval and other suitable cross-sections or other shapes, such as dumbbell, kidney-shaped, triangular or trilobal or multilobal cross-sections. Hollow fibers are preferably used.
Polyesterfasern haben im Allgemeinen Titerwerte im Bereich von 0,9 bis 16 dtex. Bevorzugt werden Polyesterhohlfasern mit den vorstehenden Werten eingesetzt, vorzugsweise mit Titern von 0,9 bis 17 dtex, besonders bevorzugt 4 bis 13 dtex. Sofern die erfindungsgemäßen Polyesterhohlfasern als Stapelfasern eingesetzt werden sollen, haben sie eine Schnittlänge (Stapellänge) von 1 bis 150 mm, bevorzugt 8 bis 100 mm und besonders bevorzugt 24 bis 80 mm.Polyester fibers generally have titer values in the range of 0.9 to 16 dtex. Polyester hollow fibers having the above values are preferably used, preferably with titres of 0.9 to 17 dtex, more preferably 4 to 13 dtex. If the polyester hollow fibers according to the invention are to be used as staple fibers, they have a cut length (staple length) of 1 to 150 mm, preferably 8 to 100 mm and particularly preferably 24 to 80 mm.
In besonderen Ausführungsformen der Erfindung bestehen die Polyesterfasern aus einem Titergemisch und/oder einem Gemisch von Fasern mit unterschiedlicher Stapellänge.In particular embodiments of the invention, the polyester fibers consist of a Titer mixture and / or a mixture of fibers with different staple length.
Sofern die erfindungsgemäßen Polyesterfasern für textile Anwendungen oder als Füllfaserpackung eingesetzt werden, ist eine Texturierung vorteilhaft, insbesondere eine Kräuselung.If the polyester fibers according to the invention are used for textile applications or as filler fiber packing, texturing is advantageous, in particular crimping.
Erfindungsgemäß beträgt der Kräuselungsgrad 2 Kräuselungen (Kräuselbögen) pro cm (Bg) oder mehr, bevorzugt 3 Bögen pro cm oder mehr.According to the invention, the degree of crimping is 2 crimps (crimps) per cm (Bg) or more, preferably 3 sheets per cm or more.
Die Anzahl der Bögen pro cm muss außerdem in einem bestimmten Verhältnis zur sog. Einkräuselung K1 stehen. K1 hat vorzugsweise Werte von mindestens 15%, bevorzugt mindestens 18%. Das Verhältnis Einkräuselung zu Anzahl Bögen pro cm liegt demzufolge bei einer Bogenzahl pro cm Bg von 3,0 bevorzugt in dem Bereich von 5 ≤ K1/Bg≤ 6.The number of sheets per cm must also be in a certain ratio to the so-called crimp K1. K1 preferably has values of at least 15%, preferably at least 18%. Accordingly, the ratio of curling to number of sheets per cm is preferably in the range of 5 ≦ K1 / Bg ≦ 6 at a number of sheets per cm Bg of 3.0.
Unter Einkräuselung im Rahmen der Erfindung versteht man folgendes Verhältnis:
Die erfindungsgemäßen flammhemmenden Fasern können zusätzlich weitere im Stand der Technik üblicherweise verwendete Additive aufweisen. Hierunter sind insbesondere Antioxidantien, Stabilisatoren (z.B. UV-Stabilisatoren), Mattierungsmittel (z.B. TiO2 Zinksulfid oder Zinkoxid), Pigmente (z.B. TiO2), zusätzliche Flammhemmmittel, Antistatikmittel, Farbstoffe, Füller (z.B. Calciumcarbonat), antimikrobielle Mittel, bioaktive Mittel, optische Aufheller, Streckmittel und weitere Verarbeitungshilfsmittel zu verstehen.The flame retardant fibers of the invention may additionally comprise other additives commonly used in the art. These include in particular antioxidants, stabilizers (eg UV stabilizers), matting agents (eg TiO 2 zinc sulfide or zinc oxide), pigments (eg TiO 2 ), additional flame retardants, antistatic agents, dyes, fillers (eg calcium carbonate), antimicrobial agents, bioactive agents, optical Brighteners, extenders and other processing aids to understand.
Derartige Additive können dem Polymer zu jedem Zeitpunkt während der Polymerherstellung zugegeben oder mit der Avivage auf die Fasern aufgegeben werden.Such additives may be added to the polymer at any time during polymer preparation or applied to the fibers with the finish.
Die Faserherstellung erfolgt, indem Polymere zu Filamenten, gegebenenfalls unter Anwendung von Gleitmitteln, versponnen und dann zu Fasern verarbeitet werden, die Fasern verstreckt und gekräuselt werden, und gegebenenfalls ein Antistatikmittel auf die Fasern aufgebracht wird. Im Falle der Herstellung von Stapelfasern werden die Fasern geschnitten und danach als sogenannte Flocke in Ballen gepresst und verpackt.Fiber fabrication is accomplished by spinning polymers into filaments, optionally with lubricants, and then processing into fibers, drawing and crimping the fibers, and optionally applying an antistatic agent to the fibers. In the case of the production of staple fibers, the fibers are cut and then pressed into so-called flake bales and packaged.
Die Herstellung der Fasern geschieht unter Anwendung konventioneller Methoden und Anlagen, wie sie auf dem Fachgebiet im Zusammenhang mit Polyesterfasern bevorzugt werden. Beispielsweise werden zahlreiche Methoden des Verspinnens in
Die Spinngeschwindigkeit beträgt vorzugsweise 800 Meter pro Minute oder mehr und beträgt im typischen Fall 1600 Meter pro Minute oder weniger. Die Spinntemperatur beträgt im typischen Fall 255°C oder mehr und 305°C oder weniger. Besonders bevorzugt wird das Spinnen bei etwa 280°C ausgeführt.The spinning speed is preferably 800 meters per minute or more, and is typically 1600 meters per minute or less. The spinning temperature is typically 255 ° C or more and 305 ° C or less. More preferably, spinning is carried out at about 280 ° C.
Die Spinndüse ist eine konventionelle Spinndüse vom Typ, wie er bei konventionellen Polyestern verwendet wird, wobei Lochgröße, Anordnung und Zahl von der gewünschten Faser und der Spinnanlage abhängen.The spinneret is a conventional spinneret of the type used in conventional polyesters, with hole size, location and number depending on the desired fiber and spin line.
Das Abschrecken der auf diese Art und Weise aus der Schmelze gesponnenen Polyesterfilamente kann in konventioneller Weise ausgeführt werden, indem Luft oder andere Fluide verwendet werden, wie sie im Fachgebiet beschrieben werden (z.B. Stickstoff). Es können Querstrom-, Radial-, asymmetrische oder andere Kühlmethoden angewendet werden. Bevorzugt wird zum Abschrecken mit Luft angeblasen.Quenching of the melt-spun polyester filaments in this manner may be carried out in a conventional manner using air or other fluids as described in the art (e.g., nitrogen). Cross-flow, radial, asymmetric or other cooling methods can be used. It is preferred to blow with air for quenching.
Nach dem Kühlen können konventionelle Spinnzusätze mit Hilfe von Standardmethoden aufgetragen werden.After cooling, conventional spin finishes can be applied using standard techniques.
Die so hergestellten Faserfilamente werden zur weiteren Verarbeitung zunächst in Kannen abgelegt.The fiber filaments thus produced are first deposited in cans for further processing.
Nach einem bevorzugten Verfahren werden die schmelzgesponnenen Faserfilamente auf einem Spinnkabelzylinder aufgenommen und anschließend mehrere Spinnkabelzylinder zusammengesetzt und aus den Faserfilamenten ein großes Spinnkabel erzeugt. Danach können die Faserkabel unter Anwendung konventioneller Methoden verstreckt werden, vorzugsweise bei 10 bis 110 m/min. Die Streckverhältnisse reichen bevorzugt von 1,25 bis 4, stärker bevorzugt von 2,5 bis 3,5, besonders bevorzugt liegt es bei 3,2. Die Temperatur bei der Verstreckung liegt im Bereich der Glasumwandlungstemperatur des zu verstreckenden Polyesterkabels und beträgt bevorzugt 40°C bis 80°C und liegt besonders bevorzugt bei 69°C. Die Nachbehandlung wird bei ca. 150° bis 165°C durchgeführt, um eine gute Trocknung zu gewährleisten. Das Verstrecken kann wahlweise unter Anwendung eines zweistufigen Streckprozesses ausgeführt werden (siehe hierzu beispielsweise die
Bevorzugt wird die erfindungsgemäße silikonfreie Weichgriffausrüstung zwischen der Verstreckung und der Kräuselung aufgebracht. Das Aufbringen erfolgt mit üblichen Techniken, insbesondere durch Besprühen oder mittels einer Auftragswalze. Die aufgebrachte Menge beträgt zwischen 0,4 und 0,5% des Fasergewichtes und liegt bevorzugt bei 0,46%.Preferably, the silicone-free soft-grip equipment according to the invention is applied between the stretching and the crimping. The application is carried out by conventional techniques, in particular by spraying or by means of an applicator roll. The amount applied is between 0.4 and 0.5% of the fiber weight and is preferably 0.46%.
Für die Kräuselung der so gestreckten Fasern können konventionelle Methoden der mechanischen Kräuselung mit an sich bekannten Kräuselmaschinen angewendet werden. Bevorzugt ist eine mechanische Vorrichtung zur Stapelfaserkräuselung mit Dampfunterstützung, wie beispielsweise eine Stauchkammer. Es können aber auch nach anderen Verfahren gekräuselte Fasern eingesetzt werden, so z.B. auch dreidimensionalgekräuselte Fasern. Zur Durchführung der Kräuselung wird das Kabel zunächst auf eine Temperatur im Bereich von 60° bis 100°C, bevorzugt 70° bis 85°C, besonders bevorzugt auf etwa 83°C erwärmt und mit einem Druck der Kabeleinlaufwalzen von 1,0 bis 2,0 bar, besonders bevorzugt bei etwa 1,5 bar, einem Druck in der Kräuselkammer von 0,5 bis 1,0 bar, besonders bevorzugt 0,8 bar, mit Dampf bei zwischen 1,0 und 2,0 kg/min., besonders bevorzugt 1,5 kg/min., behandelt.For the crimping of the fibers thus stretched, conventional methods of mechanical crimping can be used with known crimping machines. Preferred is a mechanical device for staple fiber crimping with steam assist, such as a stuffer box. However, crimped fibers can also be used according to other methods, for example also three-dimensionally crimped fibers. To carry out the crimping, the cable is first heated to a temperature in the range of 60 ° to 100 ° C., preferably 70 ° to 85 ° C., particularly preferably about 83 ° C., and with a pressure of the cable entry rollers of 1.0 to 2, 0 bar, more preferably at about 1.5 bar, a pressure in the crimping chamber of 0.5 to 1.0 bar, particularly preferably 0.8 bar, with steam at between 1.0 and 2.0 kg / min., especially preferably 1.5 kg / min, treated.
Unter Anwendung konventioneller Methoden kann in der Kräuselvorrichtung eine weitere Appretur aufgebracht werden.Using conventional methods, another finish can be applied in the crimper.
Die Fasern werden bei 150° bis 165°C im Ofen relaxiert und/oder fixiert werden. Die Präparation benötigt keinen eigenen Fixierschritt.The fibers are relaxed at 150 ° to 165 ° C in the oven and / or fixed. The preparation does not need its own fixation step.
Wahlweise kann auf die Fasern nach dem Relaxieren eine antistatische Ausrüstung aufgebracht werden.Optionally, antistatic finish may be applied to the fibers after relaxation.
Weiterhin können die Fasern, falls erwünscht, pillarm ausgerüstet werden.Furthermore, if desired, the fibers can be made pillar free.
Zur Herstellung von Stapelfasern werden die texturierten Fasern aufgenommen, gefolgt von Schneiden und gegebenenfalls Härten und Ablage in gepressten Ballen als Flocke. Die Stapelfasern der vorliegenden Erfindung werden bevorzugt auf einer der Relaxation nachgeschalteten mechanischen Schneidvorrichtung geschnitten. Zur Herstellung von Kabeltypen kann auf das Schneiden verzichtet werden. Diese Kabeltypen werden in ungeschnittener Form im Ballen abgelegt und verpresst.To make staple fibers, the textured fibers are taken up, followed by cutting and possibly hardening and depositing in pressed bales as a flake. The staple fibers of the present invention are preferably cut on a relaxation downstream mechanical cutter. For the production of cable types can be dispensed with the cutting. These cable types are placed in uncut form in the bale and pressed.
Weiterer Gegenstand ist die Verwendung der erfindungsgemäßen Faserprodukte als Faserfüllstoffe oder in textilen Flächengebilden.Another object is the use of the fiber products according to the invention as fiber fillers or in textile fabrics.
Die Verwendung der erfindungsgemäßen Faserprodukte als Faserfüllstoffe beinhaltet Füllungen für gefüllte Bezüge, wie z.B. Kopfkissen, Steppbetten, Steppdecken und dergleichen, sowie für Matratzen und Schlafsäcke, Dämmmaterial und Polsterungen, beispielsweise für Möbel und im Automobilbereich, sowie Filter.The use of the fiber products of the present invention as fibrous fillers includes fillings for filled covers, e.g. Pillows, duvets, quilts and the like, as well as for mattresses and sleeping bags, insulation and upholstery, for example for furniture and in the automotive sector, as well as filters.
Erfindungsgemäße textile Flächengebilde sind beispielsweise Bekleidung, die Ober- und Unterbahnen der oben genannten Bezüge, sowie Matratzenauflagen.Inventive textile fabrics are, for example, clothing, the upper and lower webs of the above-mentioned covers, as well as mattress pads.
Die Erfindung wird anhand des folgenden Beispiels näher erläutert:The invention will be explained in more detail with reference to the following example:
Eine Stapelfaser mit Hohlprofil wird in der für Fasern aus dem flammhemmenden Rohstoff üblichen Weise aus der Schmelze gesponnen, durch Anblasen mit Luft abgekühlt, mit üblicher Stapelfaserpräparation versehen und für die Verarbeitung auf der Bandstrasse in Kannen abgelegt.A staple fiber with a hollow profile is spun from the melt in the usual way for fibers from the flame-retardant raw material, cooled by blowing with air, provided with conventional staple fiber preparation and stored in cans for processing on the strip line.
Die Spinnware wird als Faserkabel über einen Einlaufrechen gesammelt und von einem ersten Septett, aus sieben rotierenden Walzen bestehend, eingezogen, durch ein Tauchbad geführt, wo es temperiert und nochmals mit Präparation versehen wird. Die Spinnware wird von einem weiteren Septett weitertransportiert. Auf der 6. oder 7. Walze dieses Septetts bzw. zwischen diesem und einem weiteren, um den Faktor der Verstreckung schneller laufenden Septett erfolgt die Verstreckung. Im Anschluss daran wird die Faser in einer Stauchkammer gekräuselt, im Ofen fixiert bzw. getrocknet und ggf. geschnitten. Zwischen Verstreckung und Kräuselung erfolgt die Zugabe einer silikonfreien Weichgriffausrüstung durch Besprühung oder mittels Auftragswalze.The spun goods are collected as a fiber cable via an inlet rake and fed by a first septet, consisting of seven rotating rollers, passed through a dip bath, where it is tempered and again provided with preparation. The spun goods are transported by another septet. The stretching takes place on the sixth or seventh roll of this septet or between this and a further septet running faster by the factor of stretching. Subsequently, the fiber is crimped in a stuffer box, fixed in the oven or dried and optionally cut. Between drawing and crimping, the addition of a silicone-free softening equipment by spraying or by application roller.
An den hergestellten Fasern werden folgende textiltechnologischen Werte ermittelt:
Claims (29)
R5-COOH,
R 5 -COOH,
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DK08016820T DK2169110T3 (en) | 2008-09-25 | 2008-09-25 | Flame retardant hollow fibers equipped with silicone-free soft grip comprising a polyether and a fatty acid condensation product |
EP20080016820 EP2169110B1 (en) | 2008-09-25 | 2008-09-25 | Fire-resistant hollow fibres with silicon-free soft hand finish comprising a polyether and a condensation product of fatty acid |
PL08016820T PL2169110T3 (en) | 2008-09-25 | 2008-09-25 | Fire-resistant hollow fibres with silicon-free soft hand finish comprising a polyether and a condensation product of fatty acid |
US13/120,434 US20110274869A1 (en) | 2008-09-25 | 2009-09-23 | Flame-retardant hollow fiber with silicone-free soft-touch finish |
PCT/EP2009/006852 WO2010034471A1 (en) | 2008-09-25 | 2009-09-23 | Flame-retardant hollow fiber with silicone-free soft-touch finish |
JP2011528237A JP5450631B2 (en) | 2008-09-25 | 2009-09-23 | Flame retardant hollow fiber with silicone-free flexible feel finish |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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EP20080016820 EP2169110B1 (en) | 2008-09-25 | 2008-09-25 | Fire-resistant hollow fibres with silicon-free soft hand finish comprising a polyether and a condensation product of fatty acid |
Publications (2)
Publication Number | Publication Date |
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EP2169110A1 true EP2169110A1 (en) | 2010-03-31 |
EP2169110B1 EP2169110B1 (en) | 2013-06-05 |
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EP20080016820 Active EP2169110B1 (en) | 2008-09-25 | 2008-09-25 | Fire-resistant hollow fibres with silicon-free soft hand finish comprising a polyether and a condensation product of fatty acid |
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US (1) | US20110274869A1 (en) |
EP (1) | EP2169110B1 (en) |
JP (1) | JP5450631B2 (en) |
DK (1) | DK2169110T3 (en) |
PL (1) | PL2169110T3 (en) |
WO (1) | WO2010034471A1 (en) |
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US11014030B2 (en) | 2016-02-17 | 2021-05-25 | Hollingsworth & Vose Company | Filter media including flame retardant fibers |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN112971488A (en) * | 2021-02-24 | 2021-06-18 | 安徽万利达羽绒制品有限公司 | Preparation frock that eiderdown fine hair filling was used |
CN112971488B (en) * | 2021-02-24 | 2022-09-02 | 安徽万利达羽绒制品有限公司 | Preparation frock that eiderdown fine hair filling was used |
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US20110274869A1 (en) | 2011-11-10 |
DK2169110T3 (en) | 2013-09-08 |
JP2012503720A (en) | 2012-02-09 |
EP2169110B1 (en) | 2013-06-05 |
JP5450631B2 (en) | 2014-03-26 |
WO2010034471A1 (en) | 2010-04-01 |
PL2169110T3 (en) | 2013-11-29 |
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