US20030143396A1 - Abrasion-resistant spun articles - Google Patents
Abrasion-resistant spun articles Download PDFInfo
- Publication number
- US20030143396A1 US20030143396A1 US10/376,285 US37628503A US2003143396A1 US 20030143396 A1 US20030143396 A1 US 20030143396A1 US 37628503 A US37628503 A US 37628503A US 2003143396 A1 US2003143396 A1 US 2003143396A1
- Authority
- US
- United States
- Prior art keywords
- yarns
- fibers
- filaments
- particles
- resin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000005299 abrasion Methods 0.000 title claims abstract description 26
- 239000000835 fiber Substances 0.000 claims abstract description 36
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 11
- 239000000057 synthetic resin Substances 0.000 claims abstract description 11
- 239000002245 particle Substances 0.000 claims description 48
- 229920005989 resin Polymers 0.000 claims description 21
- 239000011347 resin Substances 0.000 claims description 21
- 150000001875 compounds Chemical class 0.000 claims description 17
- 229920002292 Nylon 6 Polymers 0.000 claims description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 10
- 229910052901 montmorillonite Inorganic materials 0.000 claims description 8
- 239000004952 Polyamide Substances 0.000 claims description 7
- 229920002647 polyamide Polymers 0.000 claims description 7
- 230000008961 swelling Effects 0.000 claims description 6
- 229920002302 Nylon 6,6 Polymers 0.000 claims description 5
- 239000000377 silicon dioxide Substances 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 239000000155 melt Substances 0.000 claims description 4
- 150000004760 silicates Chemical class 0.000 claims description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 2
- 235000012216 bentonite Nutrition 0.000 claims description 2
- 229910052793 cadmium Inorganic materials 0.000 claims description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 claims description 2
- 230000033001 locomotion Effects 0.000 claims description 2
- 229910052618 mica group Inorganic materials 0.000 claims description 2
- 235000019355 sepiolite Nutrition 0.000 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- 239000010703 silicon Substances 0.000 claims description 2
- 235000012222 talc Nutrition 0.000 claims description 2
- 150000003568 thioethers Chemical class 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- 239000010936 titanium Substances 0.000 claims description 2
- 235000019354 vermiculite Nutrition 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- 239000010954 inorganic particle Substances 0.000 claims 1
- 238000000034 method Methods 0.000 description 15
- 229920000642 polymer Polymers 0.000 description 14
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 11
- 238000011282 treatment Methods 0.000 description 10
- 238000009987 spinning Methods 0.000 description 9
- 239000011159 matrix material Substances 0.000 description 7
- 239000004927 clay Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 238000005342 ion exchange Methods 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 150000002894 organic compounds Chemical class 0.000 description 6
- 206010042674 Swelling Diseases 0.000 description 5
- 238000010348 incorporation Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 229920006096 Technyl® Polymers 0.000 description 4
- IPTLKMXBROVJJF-UHFFFAOYSA-N azanium;methyl sulfate Chemical compound N.COS(O)(=O)=O IPTLKMXBROVJJF-UHFFFAOYSA-N 0.000 description 4
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000003760 tallow Substances 0.000 description 4
- 238000004299 exfoliation Methods 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- PBLZLIFKVPJDCO-UHFFFAOYSA-N 12-aminododecanoic acid Chemical compound NCCCCCCCCCCCC(O)=O PBLZLIFKVPJDCO-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
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 150000002892 organic cations Chemical class 0.000 description 2
- 229910052615 phyllosilicate Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- FWLORMQUOWCQPO-UHFFFAOYSA-N benzyl-dimethyl-octadecylazanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 FWLORMQUOWCQPO-UHFFFAOYSA-N 0.000 description 1
- PNCQLRYMHQOAOR-UHFFFAOYSA-N bis(2-hydroxyethyl)-methyl-octadecylazanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(CCO)CCO PNCQLRYMHQOAOR-UHFFFAOYSA-N 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- OGQYPPBGSLZBEG-UHFFFAOYSA-N dimethyl(dioctadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC OGQYPPBGSLZBEG-UHFFFAOYSA-N 0.000 description 1
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-O dodecylazanium Chemical compound CCCCCCCCCCCC[NH3+] JRBPAEWTRLWTQC-UHFFFAOYSA-O 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-O hydron;octadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCC[NH3+] REYJJPSVUYRZGE-UHFFFAOYSA-O 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002077 nanosphere Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- FCZSASCJWJQESY-UHFFFAOYSA-N octadecyl(triphenyl)phosphanium Chemical compound C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CCCCCCCCCCCCCCCCCC)C1=CC=CC=C1 FCZSASCJWJQESY-UHFFFAOYSA-N 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 125000005496 phosphonium group Chemical group 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 229910052698 phosphorus Chemical group 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- BJQWBACJIAKDTJ-UHFFFAOYSA-N tetrabutylphosphanium Chemical compound CCCC[P+](CCCC)(CCCC)CCCC BJQWBACJIAKDTJ-UHFFFAOYSA-N 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D02—YARNS; MECHANICAL FINISHING OF YARNS OR ROPES; WARPING OR BEAMING
- D02G—CRIMPING OR CURLING FIBRES, FILAMENTS, THREADS, OR YARNS; YARNS OR THREADS
- D02G3/00—Yarns or threads, e.g. fancy yarns; Processes or apparatus for the production thereof, not otherwise provided for
- D02G3/44—Yarns or threads characterised by the purpose for which they are designed
- D02G3/442—Cut or abrasion resistant yarns or threads
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/60—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21F—PAPER-MAKING MACHINES; METHODS OF PRODUCING PAPER THEREON
- D21F1/00—Wet end of machines for making continuous webs of paper
- D21F1/0027—Screen-cloths
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21F—PAPER-MAKING MACHINES; METHODS OF PRODUCING PAPER THEREON
- D21F7/00—Other details of machines for making continuous webs of paper
- D21F7/08—Felts
- D21F7/083—Multi-layer felts
-
- 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
-
- 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
- Y10T428/2927—Rod, strand, filament or fiber including structurally defined particulate matter
-
- 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
- Y10T428/2929—Bicomponent, conjugate, composite or collateral fibers or filaments [i.e., coextruded sheath-core or side-by-side type]
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2967—Synthetic resin or polymer
- Y10T428/2969—Polyamide, polyimide or polyester
Definitions
- the present invention relates to spun articles, yarns, fibers or filaments which have improved abrasion resistance and which can be used in particular to produce felts for paper machines.
- the invention relates more particularly to yarns, fibers or filaments based on synthetic resin and containing nanometric-sized fillers.
- the properties which spun articles need to have are different depending on their use. Among these, mention may be made, for example, of mechanical strength, transparency, gloss, whiteness, dyeing ability, shrinkage, capacity for water retention, fire resistance, stability and heat resistance.
- Another solution for improving the abrasion resistance of articles made from fibers consists in using articles with three-dimensional crimping.
- the aim of the present invention is to propose another solution for obtaining spun articles with high abrasion resistance.
- the invention proposes yarns, fibers and filaments based on synthetic resin, characterized in that they comprise between 0.05% and 20% by weight of nanometric-sized particles dispersed in the resin and in that they have an abrasion resistance which is improved by at least 5%,compared with yarns, fibers and filaments made from an identical resin, of the same viscosity but not containing nanometric-sized particles.
- the abrasion resistance is defined by the number of to and fro motions of a three-roll roller assembly, over a set of 15 fixed yarns, that is required to break 13 of the yarns.
- This solution furthermore has the advantage of being able to be combined with an improvement in the abrasion resistance by increasing the viscosity of the resin.
- nanometric-sized particle means any object for which at least one characteristic size parameter (diameter, length, thickness) is less than or equal to 100 nanometers, preferably less than or equal to 50 nm.
- the particles may be, for example, substantially spherical, with a nanometric-sized diameter.
- the particles may be in the shape of platelets or needles, i.e. shapes for which it is possible to define at least one large size parameter and at least one small size parameter.
- the small size parameter is advantageously less than 50 nm and preferably 10 nm.
- the particles may be platelets less than 10 nm thick with a form factor, .i.e. a ratio of large size to small size, of greater than 10.
- the weight proportion of the particles relative to the total weight of the material is between 0.05% and 20%. It is advantageously less than or equal to 5%.
- the synthetic resin constituting the matrix in which the particles are dispersed may be chosen from any spinnable polymer. It consists, for example, of polyamide or polyester, a blend of polymers comprising polyamide or polyester, or copolymers based on polyamide or polyester.
- polyamides which are suitable for carrying out the invention, mention may be made in particular of Nylon-6 and Nylon-6,6, and blends and copolymers thereof.
- the yarns, fibers and filaments according to the invention may contain any additive usually used with such polymers, for example heat stabilizers, UV stabilizers, catalysts, pigments, dyes and antibacterial agents.
- the particles dispersed in the synthetic resin matrix are of substantially spherical shape with a mean diameter of less than or equal to 100 nanometers. According to one preferred embodiment, the mean diameter of these particles is less than or equal to 50 nanometers.
- the particles may be chosen from particles based on inorganic materials. They may be metallic or mineral, obtained from a natural source or may be synthesized. Examples of suitable materials which may be mentioned include silver, copper, gold and the oxides and sulfides of metals, for example of silicon, zirconium, titanium, cadmium or zinc. Silica-based particles may be used in particular.
- the particles may have been subjected to treatments to make them compatible with the matrix. These treatments are, for example, surface treatments or a surface deposition of a compound other than that constituting the core of the particles. Treatments and depositions may similarly be carried out in order to promote the dispersion of the particles, either in the polymerization medium of the matrix or in the molten polymer.
- the surface of the particles may comprise a protective layer intended to prevent any degradation of the polymer in contact with these particles.
- Metal oxides for example silica, in a continuous or discontinuous layer, may thus be deposited at the surface of the particles.
- a first process consists in melt-blending the particles in resin and in optionally subjecting the mixture to high shear, for example in a twin-screw extrusion device, in order to achieve good dispersion.
- Another process consists in mixing the particles with the monomers in the curing medium, and then in curing the resin.
- Another process consists in melt-blending a concentrated mixture of a resin and particles, prepared, for example, according to one of the processes described above.
- the particles are introduced and mixed with the monomers or the melt.
- the particles may be introduced in the form of powder or in the form of an optionally stablilized aqueous solution.
- a silica sol may be introduced into the curing medium of the resin.
- the particles dispersed in the synthetic resin matrix are in the form of platelets less than 10 nanometers thick. Preferably, the thickness is less than 5 nanometers.
- the particles are preferably dispersed in the matrix in individual form. However, aggregates may exist and are preferably less than 100 nm thick and even more preferably less than 50 nm thick.
- the platelets are advantageously obtained from exfoliable silicate leaflets.
- the exfoliation may be promoted by a prior treatment with a swelling agent, for example by exchange of the cations initially contained in the silicates with organic cations such as oniums.
- the organic cations may be chosen from phosphoniums and-ammoniums, for example primary to quaternary ammoniums. Mention may be made, for example, of protonated amino acids such as 12-aminododecanoic acid, protonated primary to tertiary ammoniums, and quaternary ammoniums.
- the chains attached to the nitrogen or phosphorus atom of the onium may be aliphatic, aromatic, aryaliphatic, linear or branched and may contain oxygenated units, for example hydroxyl or ethoxy units.
- organic ammonium treatments mention may be made of dodecylammonium, octadecylammonium, bis(2-hydroxyethyl)octadecylmethyl-ammonium, dimethyldioctadecylammonium, octadecylbenzyl-dimethylammonium and tetramethylammonium.
- alkylphosphoniums such as tetrabutylphosphonium, trioctyloctadecylphosphonium and octadecyltriphenyl-phosphonium. These lists do not have any limiting nature.
- the silicate leaflets which are suitable for carrying-out the invention may be chosen from montmorillonites, smectites, illites, sepiolites, palygorkites, muscovites, allervardites, amesites, hectorites, talcs, fluorohectorites, saponites, beidellites, nontronites, stevensites, bentonites, micas, fluoromicas, vermiculites, fluorovermiculites and halloysites. These compounds may be of natural, synthetic or modified natural origin.
- the yarns, fibers and filaments are composed of polyamide resin and of platelet particles dispersed in the resin, obtained by exfoliation of a phyllosilicate, for example a montmorillonite which has undergone a prior swelling treatment by ion exchange.
- a phyllosilicate for example a montmorillonite which has undergone a prior swelling treatment by ion exchange.
- swelling treatments which may be used are disclosed, for example, in patent EP-A-0 398 551. All the known treatments for promoting the exfoliation of phyllosilicates in a polymer matrix may be used. It is possible, for example, to use a clay treated with an organic compound sold by the company Laporte under the brand name Cloisite®.
- a first process consists in mixing the compound to be dispersed, optionally treated, for example, with a swelling agent, in the melt and in optionally subjecting the mixture to high shear, for example in a twin-screw extrusion device, in order to achieve good dispersion.
- Another process consists in mixing the compound to be dispersed, optionally treated, for example, with a swelling agent, with the monomers in the curing medium, and then in curing the resin.
- Another process consists in melt-blending a concentrated mixture of a resin and dispersed particles, prepared, for example, according to one of the processes described above.
- the particles are introduced and mixed with the monomers or the melt.
- the particles may be introduced in the form of a powder of exfoliable compound or in the form of a dispersion in water or in an organic dispersant of an exfoliable compound.
- the spun articles, yarns, fibers or filaments are made according to the usual spinning techniques from a material comprising the synthetic resin and the particles.
- the spinning may be carried out immediately after curing the resin, this resin being in molten form. It may be carried out using a granular composite comprising the particles and the synthetic resin.
- the particles may be incorporated into the molten polymer before the spinning operation in the form of a concentrated mixture in a polymer. Any method for incorporating particles into a polymer to be spun may be used.
- the spun articles according to the invention may be subjected to any treatment which may be carried out in steps subsequent to the spinning step. They may in particular be drawn, textured, crimped, heated, twisted, dyed, sized, chopped, etc. These additional operations may be carried out continuously and may be incorporated after the spinning device or may be carried out in batchwise mode. The list of operations subsequent to the spinning operation has no limiting nature.
- the spun articles according to the invention may be used in woven, knitted or nonwoven form.
- the fibers according to the invention are suitable in particular for the manufacture of felts for paper machines. They may also be used for the manufacture of yarns for carpets.
- Abrasion resistance a simultaneous friction is applied to 15 immobile yarns whose tension is kept constant at 15 yarns by 3 brass rolls forming a roller assembly. The point of application of the rolling zone is moved along the yarns over an amplitude of 90 mm at a frequency of 220 cycles per minute. The abrasion resistance is defined by the number of cycles (to and fro) required to break 13 of the 15 yarns. The measurements given are the averages of the values obtained on three tests with similar yarns.
- the sol is introduced as an aqueous phase at a weight concentration of 30%.
- the curing of the caprolactam is carried out according to a usual process. After curing, a polymer is obtained with an absolute molar mass of 34 980 g/mol, determined by GC, and a viscosity index of 140 ml/g. The polymer is washed and then dried for 16 hours at 110° C. under a primary vacuum.
- the polymer is then spun at low speed in the form of a round monofilament through a die about 1 mm in diameter.
- the yarn obtained has a diameter of about 250 ⁇ m.
- the yarn is then drawn by pinching between two rollers.
- the draw ratio is equal to the ratio of the rotation speeds of the rollers. Different draw ratios are applied.
- Nylon-6 a sodium montmorillonite which has undergone an ion exchange with dimethyl-2-ethylhexyl-(hydrogenated tallow)ammonium methyl sulfate, of 95 to 100 milliequivalents per 100 g of montmorillonite, is introduced into Nylon-6.
- Nylon-6 is a commercial compound with a viscosity index of 140 ml/g, sold under the name Technyl®. The incorporation is carried out in a Leistritz twin-screw extruder with a diameter of 34 mm.
- Nylon-6 a sodium montmorillonite which has undergone an ion exchange with dimethyl-2-ethylhexyl-(hydrogenated tallow)ammonium methyl sulfate, of 95 to 100 milliequivalents per 100 g of montmorillonite, is introduced into Nylon-6.
- Nylon-6 is a commercial compound with a viscosity index of 140 ml/g, sold under the name Technyl®. The incorporation is carried out in a Leistritz twin-screw extruder with a diameter of 34 mm.
- the characteristics of the yarns obtained are as follows: Elongation Tensile 5% Secant Abrasion at break strength modulus resistance Draw ratio (%) (MPa) (MPa) (cycles) Example 5 4.10 30.0 519 3.52 6 300 Example 6 4.65 19.6 625 4.21 5 500
- Nylon-6 a sodium montmorillonite which has undergone an ion exchange with dimethyl-2-ethylhexyl-(hydrogenated tallow)ammonium methyl sulfate, of 95 to 100 milliequivalents per 100 g of montmorillonite, is introduced into Nylon-6.
- Nylon-6 is a commercial compound with a viscosity index of 140 ml/g, sold under the name Technyl®. The incorporation is carried out in a Leistritz twin-screw extruder with a diameter of 34 mm.
- Nylon-6 5% by weight of a clay treated with an organic compound sold by the company Laporte, a sodium montmorillonite which has undergone an ion exchange with dimethyldioctadecylammonium chloride, of 120 milliequivalents per lo g of montmorillonite, is introduced into Nylon-6.
- Nylon-6 is a commercial compound with a viscosity index of 140 ml/g, sold under the name Technyl®. The incorporation is carried out in a Leistritz twin-screw extruder with a diameter of 34 mm.
- Nylon-6,6 is a commercial compound with a viscosity index of 140 ml/g, sold by the company Nyltech. The incorporation is carried out in a Leistritz twin-screw extruder with a diameter of 34 mm.
- the characteristics of the yarns obtained are as follows: Elongation Tensile 5% Secant Abrasion at break strength modulus resistance Draw ratio (%) (MPa) (MPa) (cycles) Example 11 3.94 25.0 372 3.7 5 200 Example 12 4.72 17.1 501 4.7 4 200
- a Nylon-6 with a viscosity of 140 ml/g is spun and drawn under the same conditions as those described in Examples 3 to 10.
- a Nylon-6,6 with a viscosity index of 140 ml/g is spun and drawn under the same conditions as those described in Examples 11 and 12.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Artificial Filaments (AREA)
Abstract
The invention relates to spun articles, threads (yarns), fibers or filaments which have improved abrasion resistance properties and which can be used to produce felts for paper machines. The invention more specifically relates to synthetic resin-based threads (yarns), fibers or filaments having nanometric-sized loads.
Description
- The present invention relates to spun articles, yarns, fibers or filaments which have improved abrasion resistance and which can be used in particular to produce felts for paper machines. The invention relates more particularly to yarns, fibers or filaments based on synthetic resin and containing nanometric-sized fillers.
- The properties which spun articles need to have are different depending on their use. Among these, mention may be made, for example, of mechanical strength, transparency, gloss, whiteness, dyeing ability, shrinkage, capacity for water retention, fire resistance, stability and heat resistance. One property which may be demanded, in particular for applications in industrial fields or the fields of so-called technical yarn, is abrasion resistance.
- This is the case, for example, for the manufacture of nonwoven felts from fibers. Increasing the abrasion resistance generally makes it possible to increase the lifetime of the articles manufactured from yarns, fibers or filaments. In the case of felts for paper machines, which are made from synthetic fibers, this property has become critical following the replacement of chemical bleaching agents with solid particles, for example calcium carbonate.
- This is also the case, for example, for the manufacture of rugs and carpets from fibers. In this case, the mechanical rubbing or abrasion stresses on the rug or carpet are such that the abrasion resistance property directly characterizes the lifetime of the rug or carpet.
- One known solution for improving the abrasion resistance of spun articles is to increase the degree of curing of the synthetic material from which they are made. This is the way in which fibers made from thermoplastic resins of increasingly high viscosity are developed. Patent US-A-5 234 644 discloses, for example, a process for increasing the viscosity of polymers. However, this solution has limits. Specifically, the spinning of fibers of very high viscosity requires the use of very high spinning pressures and/or very high spinning temperatures, which may result in degradation of the polymer.
- Another solution for improving the abrasion resistance of articles made from fibers consists in using articles with three-dimensional crimping.
- The aim of the present invention is to propose another solution for obtaining spun articles with high abrasion resistance.
- To this end, the invention proposes yarns, fibers and filaments based on synthetic resin, characterized in that they comprise between 0.05% and 20% by weight of nanometric-sized particles dispersed in the resin and in that they have an abrasion resistance which is improved by at least 5%,compared with yarns, fibers and filaments made from an identical resin, of the same viscosity but not containing nanometric-sized particles. The abrasion resistance is defined by the number of to and fro motions of a three-roll roller assembly, over a set of 15 fixed yarns, that is required to break 13 of the yarns.
- This solution furthermore has the advantage of being able to be combined with an improvement in the abrasion resistance by increasing the viscosity of the resin.
- The expression “nanometric-sized particle” means any object for which at least one characteristic size parameter (diameter, length, thickness) is less than or equal to 100 nanometers, preferably less than or equal to 50 nm. The particles may be, for example, substantially spherical, with a nanometric-sized diameter. The particles may be in the shape of platelets or needles, i.e. shapes for which it is possible to define at least one large size parameter and at least one small size parameter. In this case, the small size parameter is advantageously less than 50 nm and preferably 10 nm. For example, the particles may be platelets less than 10 nm thick with a form factor, .i.e. a ratio of large size to small size, of greater than 10.
- The weight proportion of the particles relative to the total weight of the material is between 0.05% and 20%. It is advantageously less than or equal to 5%.
- The synthetic resin constituting the matrix in which the particles are dispersed may be chosen from any spinnable polymer. It consists, for example, of polyamide or polyester, a blend of polymers comprising polyamide or polyester, or copolymers based on polyamide or polyester. As examples of polyamides which are suitable for carrying out the invention, mention may be made in particular of Nylon-6 and Nylon-6,6, and blends and copolymers thereof.
- The yarns, fibers and filaments according to the invention may contain any additive usually used with such polymers, for example heat stabilizers, UV stabilizers, catalysts, pigments, dyes and antibacterial agents.
- According to a first embodiment of the invention, the particles dispersed in the synthetic resin matrix are of substantially spherical shape with a mean diameter of less than or equal to 100 nanometers. According to one preferred embodiment, the mean diameter of these particles is less than or equal to 50 nanometers.
- The particles may be chosen from particles based on inorganic materials. They may be metallic or mineral, obtained from a natural source or may be synthesized. Examples of suitable materials which may be mentioned include silver, copper, gold and the oxides and sulfides of metals, for example of silicon, zirconium, titanium, cadmium or zinc. Silica-based particles may be used in particular.
- The particles may have been subjected to treatments to make them compatible with the matrix. These treatments are, for example, surface treatments or a surface deposition of a compound other than that constituting the core of the particles. Treatments and depositions may similarly be carried out in order to promote the dispersion of the particles, either in the polymerization medium of the matrix or in the molten polymer.
- The surface of the particles may comprise a protective layer intended to prevent any degradation of the polymer in contact with these particles. Metal oxides, for example silica, in a continuous or discontinuous layer, may thus be deposited at the surface of the particles.
- Any method for obtaining a dispersion of particles in a resin may be used to carry out the invention. A first process consists in melt-blending the particles in resin and in optionally subjecting the mixture to high shear, for example in a twin-screw extrusion device, in order to achieve good dispersion. Another process consists in mixing the particles with the monomers in the curing medium, and then in curing the resin. Another process consists in melt-blending a concentrated mixture of a resin and particles, prepared, for example, according to one of the processes described above.
- There is no limitation on the form in which the particles are introduced and mixed with the monomers or the melt. The particles may be introduced in the form of powder or in the form of an optionally stablilized aqueous solution. For example, a silica sol may be introduced into the curing medium of the resin.
- According to a second embodiment of the resin, the particles dispersed in the synthetic resin matrix are in the form of platelets less than 10 nanometers thick. Preferably, the thickness is less than 5 nanometers. The particles are preferably dispersed in the matrix in individual form. However, aggregates may exist and are preferably less than 100 nm thick and even more preferably less than 50 nm thick.
- The platelets are advantageously obtained from exfoliable silicate leaflets. The exfoliation may be promoted by a prior treatment with a swelling agent, for example by exchange of the cations initially contained in the silicates with organic cations such as oniums. The organic cations may be chosen from phosphoniums and-ammoniums, for example primary to quaternary ammoniums. Mention may be made, for example, of protonated amino acids such as 12-aminododecanoic acid, protonated primary to tertiary ammoniums, and quaternary ammoniums. The chains attached to the nitrogen or phosphorus atom of the onium may be aliphatic, aromatic, aryaliphatic, linear or branched and may contain oxygenated units, for example hydroxyl or ethoxy units. As examples of organic ammonium treatments, mention may be made of dodecylammonium, octadecylammonium, bis(2-hydroxyethyl)octadecylmethyl-ammonium, dimethyldioctadecylammonium, octadecylbenzyl-dimethylammonium and tetramethylammonium. As examples of organic phosphonium treatments, mention may be made of alkylphosphoniums such as tetrabutylphosphonium, trioctyloctadecylphosphonium and octadecyltriphenyl-phosphonium. These lists do not have any limiting nature.
- The silicate leaflets which are suitable for carrying-out the invention may be chosen from montmorillonites, smectites, illites, sepiolites, palygorkites, muscovites, allervardites, amesites, hectorites, talcs, fluorohectorites, saponites, beidellites, nontronites, stevensites, bentonites, micas, fluoromicas, vermiculites, fluorovermiculites and halloysites. These compounds may be of natural, synthetic or modified natural origin.
- According to one preferred embodiment of the invention, the yarns, fibers and filaments are composed of polyamide resin and of platelet particles dispersed in the resin, obtained by exfoliation of a phyllosilicate, for example a montmorillonite which has undergone a prior swelling treatment by ion exchange. Examples of swelling treatments which may be used are disclosed, for example, in patent EP-A-0 398 551. All the known treatments for promoting the exfoliation of phyllosilicates in a polymer matrix may be used. It is possible, for example, to use a clay treated with an organic compound sold by the company Laporte under the brand name Cloisite®.
- Any method for obtaining a dispersion of particles in a resin may be used to carry out the invention. A first process consists in mixing the compound to be dispersed, optionally treated, for example, with a swelling agent, in the melt and in optionally subjecting the mixture to high shear, for example in a twin-screw extrusion device, in order to achieve good dispersion. Another process consists in mixing the compound to be dispersed, optionally treated, for example, with a swelling agent, with the monomers in the curing medium, and then in curing the resin. Another process consists in melt-blending a concentrated mixture of a resin and dispersed particles, prepared, for example, according to one of the processes described above.
- There is no limitation on the form in which the particles are introduced and mixed with the monomers or the melt. The particles may be introduced in the form of a powder of exfoliable compound or in the form of a dispersion in water or in an organic dispersant of an exfoliable compound.
- The spun articles, yarns, fibers or filaments are made according to the usual spinning techniques from a material comprising the synthetic resin and the particles. The spinning may be carried out immediately after curing the resin, this resin being in molten form. It may be carried out using a granular composite comprising the particles and the synthetic resin. The particles may be incorporated into the molten polymer before the spinning operation in the form of a concentrated mixture in a polymer. Any method for incorporating particles into a polymer to be spun may be used.
- The spun articles according to the invention may be subjected to any treatment which may be carried out in steps subsequent to the spinning step. They may in particular be drawn, textured, crimped, heated, twisted, dyed, sized, chopped, etc. These additional operations may be carried out continuously and may be incorporated after the spinning device or may be carried out in batchwise mode. The list of operations subsequent to the spinning operation has no limiting nature.
- The spun articles according to the invention may be used in woven, knitted or nonwoven form. The fibers according to the invention are suitable in particular for the manufacture of felts for paper machines. They may also be used for the manufacture of yarns for carpets.
- Other details or advantages of the invention will emerge more clearly in the light of the example below, which is given purely as a guide.
- The properties and characteristics of the yarns according to the invention are determined according to the following methods:
- Mechanical characterization (elongation at break, tensile strength): carried out on an Erichsen tensile machine placed in an air-conditioned location at 50% RH and 23° C. after conditioning the yarns for 72 hours under these conditions. The initial length of the yarns is 50 mm and the traveling speed is 50 mm/min.
- Abrasion resistance: a simultaneous friction is applied to 15 immobile yarns whose tension is kept constant at 15 yarns by 3 brass rolls forming a roller assembly. The point of application of the rolling zone is moved along the yarns over an amplitude of 90 mm at a frequency of 220 cycles per minute. The abrasion resistance is defined by the number of cycles (to and fro) required to break 13 of the 15 yarns. The measurements given are the averages of the values obtained on three tests with similar yarns.
- A sol of silica nanospheres of the brand name Klebosol® with a mean diameter equal to 50 nm, sold by the company Hoechst, is introduced into caprolactam. The sol is introduced as an aqueous phase at a weight concentration of 30%.
- The curing of the caprolactam is carried out according to a usual process. After curing, a polymer is obtained with an absolute molar mass of 34 980 g/mol, determined by GC, and a viscosity index of 140 ml/g. The polymer is washed and then dried for 16 hours at 110° C. under a primary vacuum.
- The polymer is then spun at low speed in the form of a round monofilament through a die about 1 mm in diameter. The yarn obtained has a diameter of about 250 μm. The yarn is then drawn by pinching between two rollers. The draw ratio is equal to the ratio of the rotation speeds of the rollers. Different draw ratios are applied.
- The characteristics of the yarns obtained are as follows:
Elongation Tensile 5% Secant Abrasion at break strength modulus resistance Draw ratio (%) (MPa) (MPa) (cycles) Example 1 4.37 28.8 752 2.44 1 875 Example 2 5.04 21.9 868 3.04 1 375 - 5% by weight of a clay treated with an organic compound sold by the company Laporte under the name Cloisite 25A, a sodium montmorillonite which has undergone an ion exchange with dimethyl-2-ethylhexyl-(hydrogenated tallow)ammonium methyl sulfate, of 95 to 100 milliequivalents per 100 g of montmorillonite, is introduced into Nylon-6. Nylon-6 is a commercial compound with a viscosity index of 140 ml/g, sold under the name Technyl®. The incorporation is carried out in a Leistritz twin-screw extruder with a diameter of 34 mm.
- The compound obtained is spun and drawn under the same conditions as those described in Examples 1 and 2.
- The characteristics of the yarns obtained are as follows:
Elongation Tensile 5% Secant Abrasion at break strength modulus resistance Draw ratio (%) (MPa) (MPa) (cycles) Example 3 4.28 27.4 491 4.68 5 200 Example 4 5.02 19.3 777 6.51 3 800 - 3% by weight of a clay treated with an organic compound sold by the company Laporte under the name Cloisite 25A, a sodium montmorillonite which has undergone an ion exchange with dimethyl-2-ethylhexyl-(hydrogenated tallow)ammonium methyl sulfate, of 95 to 100 milliequivalents per 100 g of montmorillonite, is introduced into Nylon-6. Nylon-6 is a commercial compound with a viscosity index of 140 ml/g, sold under the name Technyl®. The incorporation is carried out in a Leistritz twin-screw extruder with a diameter of 34 mm.
- The compound obtained is spun and drawn under the same conditions as those described in Examples 1 and 2.
- The characteristics of the yarns obtained are as follows:
Elongation Tensile 5% Secant Abrasion at break strength modulus resistance Draw ratio (%) (MPa) (MPa) (cycles) Example 5 4.10 30.0 519 3.52 6 300 Example 6 4.65 19.6 625 4.21 5 500 - 1% by weight of a clay treated with an organic compound sold by the company Laporte under the name Cloisite 25A, a sodium montmorillonite which has undergone an ion exchange with dimethyl-2-ethylhexyl-(hydrogenated tallow)ammonium methyl sulfate, of 95 to 100 milliequivalents per 100 g of montmorillonite, is introduced into Nylon-6. Nylon-6 is a commercial compound with a viscosity index of 140 ml/g, sold under the name Technyl®. The incorporation is carried out in a Leistritz twin-screw extruder with a diameter of 34 mm.
- The compound obtained is spun and drawn under the same conditions as those described in Examples 1 and 2.
- The characteristics of the yarns obtained are as follows:
Elongation Tensile 5% Secant Abrasion at break strength modulus resistance Draw ratio (%) (MPa) (MPa) (cycles) Example 7 4.15 31.0 563 3.84 6 400 Example 8 4.78 24.3 685 4.57 4 400 - 5% by weight of a clay treated with an organic compound sold by the company Laporte, a sodium montmorillonite which has undergone an ion exchange with dimethyldioctadecylammonium chloride, of 120 milliequivalents per lo g of montmorillonite, is introduced into Nylon-6. Nylon-6 is a commercial compound with a viscosity index of 140 ml/g, sold under the name Technyl®. The incorporation is carried out in a Leistritz twin-screw extruder with a diameter of 34 mm.
- The compound obtained is spun and drawn under the same conditions as those described in Examples 1 and 2.
- The characteristics of the yarns obtained are as follows:
Elongation Tensile 5% Secant Abrasion at break strength modulus resistance Draw ratio (%) (MPa) (MPa) (cycles) Example 9 4.62 23.8 528 2.66 2 300 Example 10 5.33 17.0 650 4.28 1 575 - 5% by weight of a clay treated with an organic compound sold by the company Laporte, a sodium montmorillonite which has undergone an ion exchange with methyl-N,N-bis(hydroxyethyl)(ester of hydrogenated 2-hydroxyethyl tallow)ammonium methyl sulfate, of 95 to 120 milliequivalents per 100 g of montmorillonite, is introduced into Nylon-6,6. Nylon-6,6 is a commercial compound with a viscosity index of 140 ml/g, sold by the company Nyltech. The incorporation is carried out in a Leistritz twin-screw extruder with a diameter of 34 mm.
- The compound obtained is spun and drawn under the same conditions as those described, in Examples 1 and 2.
- The characteristics of the yarns obtained are as follows:
Elongation Tensile 5% Secant Abrasion at break strength modulus resistance Draw ratio (%) (MPa) (MPa) (cycles) Example 11 3.94 25.0 372 3.7 5 200 Example 12 4.72 17.1 501 4.7 4 200 - A Nylon-6 with a viscosity of 140 ml/g is spun and drawn under the same conditions as those described in Examples 3 to 10.
- The characteristics of the yarns obtained are as follows:
Elongation Tensile 5% Secant Abrasion at break strength modulus resistance Draw ratio (%) (MPa) (MPa) (cycles) Comparative 4.34 33.7 660 3.72 1 700 Example 11 Comparative 5.16 20.0 975 5.74 1 000 Example 21 - A Nylon-6,6 with a viscosity index of 140 ml/g is spun and drawn under the same conditions as those described in Examples 11 and 12.
- The characteristics of the yarns obtained are as follows:
Elongation Tensile 5% Secant Abrasion at break strength modulus resistance Draw ratio (%) (MPa) (MPa) (cycles) Comparative 4.09 37.5 480 3.3 5 050 Example 3 Comparative 4.85 22.2 672 4.2 3 000 Example 4
Claims (19)
1. Yarns, fibers and filaments based on synthetic resin, characterized in that they comprise between 0.05% and 20% by weight of nanometric-sized particles dispersed in the resin and in that they have an abrasion resistance which is improved by at least 5% compared with yarns, fibers and filaments made from an identical resin, of the same viscosity but not containing nanometric-sized particles, the abrasion resistance being defined by the number of to and fro motions of a three-roll roller assembly, over a set of 15 fixed yarns, that is required to break 13 of the yarns.
2. The yarns, fibers and filaments as claimed in claim 1 , characterized in that the abrasion resistance is improved by at least 10%.
3. The yarns, fibers and filaments as claimed in claim 1 , characterized in that the weight concentration of particles is less than or equal to 5%.
4. The yarns, fibers and filaments as claimed in one of the preceding claims, characterized in that the synthetic resin is chosen from polyamides, blends containing polyamides, and copolymers based on polyamides.
5. The yarns, fibers and filaments as claimed in claim 4 , characterized in that the synthetic resin is based on Nylon-6, Nylon-6,6 or blends or: copolymers thereof.
6. The yarns, fibers and filaments as claimed in one of the preceding claims, characterized in that the particles are of substantially spherical shape and have a mean diameter of less than or equal to 100 nanometers.
7. The yarns, fibers and filaments as claimed in claim 6 , characterized in that the mean diameter of the particles is less than or equal to 50 nanometers.
8. The yarns, fibers and filaments as claimed in either of claims 6 and 7, characterized in that the particles are inorganic particles based on oxides or sulfides of titanium, silicon, zirconium, cadmium or zinc or are based on mixtures of these compounds.
9. The yarns, fibers and filaments as claimed in one of claims 6 to 8 , characterized in that the particles are based on silica.
10. The yarns, fibers and filaments as claimed in claim 9 , characterized in that the silica-based particles are introduced in the form of a sol into the curing medium of the resin.
11. The yarns, fibers and filaments as claimed in one of claims 1 to 5 , characterized in that the particles are in platelet form, the mean thickness of the platelets being less than 10 nanometers.
12. The yarns, fibers and filaments as claimed in claim 11 , characterized in that the platelets are exfoliable silicates.
13. The yarns, fibers and filaments as claimed in claim 11 , characterized in that the platelets are exfoliable silicates treated with a swelling agent.
14. The yarns, fibers and filaments as claimed in one of claims 11 to 13 , characterized in that the platelets are obtained from materials chosen from montmorillonites, smectites, illites, sepiolites, palygorkites, muscovites, allervardites, amesites, hectorites, talcs, fluorohectorites, saponites, beidellites, nontronites, stevensites, bentonites, micas, fluoromicas, vermiculites, fluorovermiculites and halloysites.
15. The yarns, fibers and filaments as claimed in one of claims 11 to 14 , characterized in that the platelets are of synthetic or natural origin.
16. The yarns, fibers and filaments as claimed in one of claims 11 to 15 , characterized in that the particles are incorporated into the resin by introduction into the curing medium of the resin.
17. The yarns, fibers and filaments as claimed in one of claims 11 to 15 , characterized in that the particles are incorporated into the resin by introduction into the melt.
18. A felt for a paper machine, made from yarns, fibers and filaments as claimed in one of claims 1 to 17 .
19. Rugs and carpets made from yarns, fibers or filaments as claimed in one of claims 1 to 17 .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/376,285 US20030143396A1 (en) | 1999-07-06 | 2003-03-03 | Abrasion-resistant spun articles |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR99/08975 | 1999-07-06 | ||
FR9908975A FR2796086B1 (en) | 1999-07-06 | 1999-07-06 | ABRASION RESISTANT WIRE ARTICLES |
US09/786,401 US6544644B1 (en) | 1999-07-06 | 2000-07-05 | Abrasion resistant spun articles |
US10/376,285 US20030143396A1 (en) | 1999-07-06 | 2003-03-03 | Abrasion-resistant spun articles |
Related Parent Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/786,401 Continuation US6544644B1 (en) | 1999-07-06 | 2000-07-05 | Abrasion resistant spun articles |
PCT/FR2000/001933 Continuation WO2001002629A1 (en) | 1999-07-06 | 2000-07-05 | Abrasion resistant spun articles |
Publications (1)
Publication Number | Publication Date |
---|---|
US20030143396A1 true US20030143396A1 (en) | 2003-07-31 |
Family
ID=9547972
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/786,401 Expired - Fee Related US6544644B1 (en) | 1999-07-06 | 2000-07-05 | Abrasion resistant spun articles |
US10/376,285 Abandoned US20030143396A1 (en) | 1999-07-06 | 2003-03-03 | Abrasion-resistant spun articles |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/786,401 Expired - Fee Related US6544644B1 (en) | 1999-07-06 | 2000-07-05 | Abrasion resistant spun articles |
Country Status (7)
Country | Link |
---|---|
US (2) | US6544644B1 (en) |
EP (1) | EP1119655A1 (en) |
CN (1) | CN1320174A (en) |
AU (1) | AU6293700A (en) |
FR (1) | FR2796086B1 (en) |
RU (1) | RU2001109248A (en) |
WO (1) | WO2001002629A1 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060058441A1 (en) * | 2004-08-28 | 2006-03-16 | Teijin Monofilament Germany Gmbh | Polyester fibers, their production and their use |
DE102005033350A1 (en) * | 2005-07-16 | 2007-01-18 | Teijin Monofilament Germany Gmbh | Polyester fibers, process for their preparation and their use |
US20070173585A1 (en) * | 2004-12-22 | 2007-07-26 | Sevenich Gregory J | Polyester nanocomposite filaments and fiber |
WO2008046476A1 (en) * | 2006-10-17 | 2008-04-24 | Dsm Ip Assets B.V. | Cut resistant yarn, a process for producing the yarn and products containing the yarn |
WO2008061229A1 (en) * | 2006-11-16 | 2008-05-22 | Appliced Nanotech Holdings, Inc. | Buffer layer for strings |
US20080206559A1 (en) * | 2007-02-26 | 2008-08-28 | Yunjun Li | Lubricant enhanced nanocomposites |
US20100295023A1 (en) * | 2009-04-06 | 2010-11-25 | Purdue Research Foundation | Field effect transistor fabrication from carbon nanotubes |
US20110098399A1 (en) * | 2009-10-24 | 2011-04-28 | Andreas Stihl Ag & Co Kg | Cutting Filament for a Trimmer and Method of Producing Such a Cutting Filament |
US8713906B2 (en) | 2006-11-16 | 2014-05-06 | Applied Nanotech Holdings, Inc. | Composite coating for strings |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BRPI0410518A (en) * | 2003-04-28 | 2006-06-20 | Rhodia Eng Plastics Srl | composition comprising at least one thermoplastic matrix, process of making a composition, process of making an article and article |
US20060205856A1 (en) * | 2004-12-22 | 2006-09-14 | Williamson David T | Compositions of polyesters and sepiolite-type clays |
DE102005005023A1 (en) * | 2005-02-03 | 2006-08-10 | Trw Automotive Safety Systems Gmbh & Co. Kg | airbag |
US7083854B1 (en) * | 2005-05-10 | 2006-08-01 | Cornell Research Foundation, Inc. | Fibers from polymer nanoclay nanocomposites by electrospinning |
FR2886949B1 (en) * | 2005-06-10 | 2007-08-03 | Rhodia Chimie Sa | POLYAMIDE THREADS, FILAMENTS AND POLYAMIDE FIBERS WITH IMPROVED PROPERTIES |
DE102005051844A1 (en) * | 2005-10-28 | 2007-05-03 | Fibertex A/S | Material with or consisting of polymer fibers |
CN101037846B (en) * | 2006-03-17 | 2010-08-11 | 中国水产科学研究院东海水产研究所 | Technique for preparing polypropylene abrasion-proof fabric riata |
US8173559B2 (en) * | 2006-11-30 | 2012-05-08 | The Procter & Gamble Company | Extensible nonwoven webs containing multicomponent nanocomposite fibers |
US8168550B2 (en) * | 2006-11-30 | 2012-05-01 | The Procter & Gamble Company | Extensible nonwoven webs containing monocomponent nanocomposite fibers |
CN102031581B (en) * | 2009-09-25 | 2012-08-29 | 上海德福伦化纤有限公司 | Method for producing super-refreshing cool-feel health care polyester fiber |
US8709959B2 (en) * | 2009-12-28 | 2014-04-29 | Kimberly-Clark Worldwide, Inc. | Puncture resistant fabric |
US20110155141A1 (en) * | 2009-12-28 | 2011-06-30 | Sawyer Lawrence H | Wearable Article That Stiffens Upon Sudden Force |
FI20115222A7 (en) | 2011-03-04 | 2012-09-05 | Metso Fabrics Oy | Paper machine fabric |
CN103147149B (en) * | 2012-11-09 | 2014-12-10 | 中国水产科学研究院东海水产研究所 | Preparation method of composite monofilament for netting gear manufacture |
CN103147151B (en) * | 2012-11-09 | 2014-12-10 | 中国水产科学研究院东海水产研究所 | Processing method of composite filament for netting gear manufacture |
KR20160101330A (en) * | 2015-02-16 | 2016-08-25 | 알이엠텍 주식회사 | micro-powder impregnated non-woven fabric and the method for preparing the same |
WO2017062067A1 (en) | 2015-10-05 | 2017-04-13 | Albany International Corp. | Compositions and methods for improved abrasion resistance of polymeric components |
CN105316791B (en) * | 2015-11-26 | 2018-01-09 | 常州灵达特种纤维有限公司 | A kind of preparation method of soft wear resistant type polyester bulk filament |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1047986B (en) * | 1952-10-21 | 1958-12-31 | Degussa | Process for the production of synthetic fiber materials |
US4739007A (en) * | 1985-09-30 | 1988-04-19 | Kabushiki Kaisha Toyota Chou Kenkyusho | Composite material and process for manufacturing same |
JPH0747644B2 (en) | 1989-05-19 | 1995-05-24 | 宇部興産株式会社 | Polyamide composite material and method for producing the same |
JP2716810B2 (en) * | 1989-08-24 | 1998-02-18 | 宇部興産株式会社 | Polyamide resin composition for filament and filament |
DE4027063C2 (en) | 1990-08-27 | 1994-02-03 | Inventa Ag | Process for the production of particularly high molecular weight polyamide fibers and polyamide fibers which can be produced by this process |
JP2000186200A (en) * | 1998-07-07 | 2000-07-04 | Unitika Ltd | Polyamide resin composition and its production |
US6066305A (en) * | 1992-02-28 | 2000-05-23 | Dugger; Cortland Otis | Production of transparent cationically-homogeneous nanostructured refractory oxides at reduced temperatures |
US5385776A (en) * | 1992-11-16 | 1995-01-31 | Alliedsignal Inc. | Nanocomposites of gamma phase polymers containing inorganic particulate material |
JP3348260B2 (en) * | 1994-06-02 | 2002-11-20 | 日本フエルト株式会社 | Felt for papermaking |
US6162530A (en) * | 1996-11-18 | 2000-12-19 | University Of Connecticut | Nanostructured oxides and hydroxides and methods of synthesis therefor |
JPH1171517A (en) * | 1997-06-20 | 1999-03-16 | Unitika Ltd | Polyamide resin composition and molded article made therefrom |
US6323270B1 (en) * | 1998-11-16 | 2001-11-27 | Case Western Reserve University | Polybenzoxazine nanocomposites of clay and method for making same |
KR100447551B1 (en) * | 1999-01-18 | 2004-09-08 | 가부시끼가이샤 도시바 | Composite Particles and Production Process Thereof, Aqueous Dispersion, Aqueous Dispersion Composition for Chemical Mechanical Polishing, and Process for Manufacture of Semiconductor Apparatus |
US6300419B1 (en) * | 1999-12-08 | 2001-10-09 | The Dow Chemical Company | Propylene polymer composition |
-
1999
- 1999-07-06 FR FR9908975A patent/FR2796086B1/en not_active Expired - Fee Related
-
2000
- 2000-07-05 RU RU2001109248/12A patent/RU2001109248A/en not_active Application Discontinuation
- 2000-07-05 AU AU62937/00A patent/AU6293700A/en not_active Abandoned
- 2000-07-05 CN CN00801633A patent/CN1320174A/en active Pending
- 2000-07-05 WO PCT/FR2000/001933 patent/WO2001002629A1/en not_active Application Discontinuation
- 2000-07-05 EP EP00949644A patent/EP1119655A1/en not_active Withdrawn
- 2000-07-05 US US09/786,401 patent/US6544644B1/en not_active Expired - Fee Related
-
2003
- 2003-03-03 US US10/376,285 patent/US20030143396A1/en not_active Abandoned
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1637633A1 (en) * | 2004-08-28 | 2006-03-22 | Teijin Monofilament Germany GmbH | Polyester fibres, method for their production and their use. |
US20060058441A1 (en) * | 2004-08-28 | 2006-03-16 | Teijin Monofilament Germany Gmbh | Polyester fibers, their production and their use |
US20070173585A1 (en) * | 2004-12-22 | 2007-07-26 | Sevenich Gregory J | Polyester nanocomposite filaments and fiber |
DE102005033350A1 (en) * | 2005-07-16 | 2007-01-18 | Teijin Monofilament Germany Gmbh | Polyester fibers, process for their preparation and their use |
US20070014989A1 (en) * | 2005-07-16 | 2007-01-18 | Hans-Joachim Bruning | Polyester fibers, their production and their use |
US8302374B2 (en) | 2006-10-17 | 2012-11-06 | Dsm Ip Assets B.V. | Cut resistant yarn, a process for producing the yarn and products containing the yarn |
WO2008046476A1 (en) * | 2006-10-17 | 2008-04-24 | Dsm Ip Assets B.V. | Cut resistant yarn, a process for producing the yarn and products containing the yarn |
US20100050309A1 (en) * | 2006-10-17 | 2010-03-04 | Marissen Roelof R | Cut resistant yarn, a process for producing the yarn and products containing the yarn |
EA014209B1 (en) * | 2006-10-17 | 2010-10-29 | ДСМ АйПи АССЕТС Б.В. | THREAD, SUSTAINABLE TO CUT, AND THE PRODUCT CONTAINING SUCH THREAD |
WO2008061229A1 (en) * | 2006-11-16 | 2008-05-22 | Appliced Nanotech Holdings, Inc. | Buffer layer for strings |
US20080124546A1 (en) * | 2006-11-16 | 2008-05-29 | Nano-Proprietary, Inc. | Buffer Layer for Strings |
US8713906B2 (en) | 2006-11-16 | 2014-05-06 | Applied Nanotech Holdings, Inc. | Composite coating for strings |
US20080206559A1 (en) * | 2007-02-26 | 2008-08-28 | Yunjun Li | Lubricant enhanced nanocomposites |
US20100295023A1 (en) * | 2009-04-06 | 2010-11-25 | Purdue Research Foundation | Field effect transistor fabrication from carbon nanotubes |
EP2314145A3 (en) * | 2009-10-24 | 2011-11-02 | Andreas Stihl AG & Co. KG | Cutting line for a string cutter and method for producing same |
US20110098399A1 (en) * | 2009-10-24 | 2011-04-28 | Andreas Stihl Ag & Co Kg | Cutting Filament for a Trimmer and Method of Producing Such a Cutting Filament |
Also Published As
Publication number | Publication date |
---|---|
CN1320174A (en) | 2001-10-31 |
US6544644B1 (en) | 2003-04-08 |
FR2796086B1 (en) | 2002-03-15 |
RU2001109248A (en) | 2003-04-10 |
WO2001002629A1 (en) | 2001-01-11 |
EP1119655A1 (en) | 2001-08-01 |
AU6293700A (en) | 2001-01-22 |
FR2796086A1 (en) | 2001-01-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6544644B1 (en) | Abrasion resistant spun articles | |
US5092381A (en) | Polyester industrial yarn and elastomeric objects reinforced with said yarn | |
RU2372422C2 (en) | Polyamide yarns, fibers and threads with improved properties | |
CA2208494C (en) | Polyamide/polyolefin bicomponent fibers and methods of making same | |
JP5141415B2 (en) | Polyester crimped multifilament and method for producing the same | |
MXPA97007067A (en) | Two-component polyamide / polyolefine fibers, novedosas and methods for elaborating | |
US5885705A (en) | Bicomponent fibers having contaminant-containing core domain and methods of making the same | |
EP0529506B1 (en) | Paper-machine felt and method of making the same | |
CA2278962A1 (en) | Monofil bicomponent fibres of the sheath/core type | |
US5780156A (en) | Biocomponet fibers having distinct crystaline and amorphous polymer domains and method making same | |
TW200304510A (en) | Process for manufacturing polypropylene monofilaments, polypropylene monofilaments and their use | |
JP2009150022A (en) | Sheath-core conjugate fiber and fiber fabric thereof | |
US4670343A (en) | Wholly aromatic polyamide fiber | |
JP5262514B2 (en) | Polyester composite fiber | |
JP2716810B2 (en) | Polyamide resin composition for filament and filament | |
JP3753658B2 (en) | Polytrimethylene terephthalate multifilament yarn | |
JPH02221412A (en) | Polyester fiber for rubber-reinforcement having improved heat-resistant adhesivity and production thereof | |
JP5262059B2 (en) | Manufacturing method of composite fiber | |
WO2017082110A1 (en) | Core-sheath composite cross-section fiber having excellent moisture absorbency and wrinkle prevention | |
JP4525082B2 (en) | Polylactic acid false twisted yarn and method for producing the same | |
US20060275604A1 (en) | Abrasion-resistant wires, fibres and filaments | |
JPS62502484A (en) | New water-dispersible synthetic fiber | |
AU2005233340B2 (en) | Polypropylene monofilaments with improved properties | |
JP2003171870A (en) | Polyketone fiber | |
JP4059192B2 (en) | Polylactic acid false twisted yarn and method for producing the same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |