AU2004299305A1 - Sized glass fibres with fast impregnation for the reinforcement of polymer materials - Google Patents
Sized glass fibres with fast impregnation for the reinforcement of polymer materials Download PDFInfo
- Publication number
- AU2004299305A1 AU2004299305A1 AU2004299305A AU2004299305A AU2004299305A1 AU 2004299305 A1 AU2004299305 A1 AU 2004299305A1 AU 2004299305 A AU2004299305 A AU 2004299305A AU 2004299305 A AU2004299305 A AU 2004299305A AU 2004299305 A1 AU2004299305 A1 AU 2004299305A1
- Authority
- AU
- Australia
- Prior art keywords
- strands
- glass
- glass strand
- strand
- polyester
- 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
- 238000005470 impregnation Methods 0.000 title description 12
- 230000002787 reinforcement Effects 0.000 title description 2
- 239000003365 glass fiber Substances 0.000 title 1
- 239000002861 polymer material Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 claims description 95
- 239000011521 glass Substances 0.000 claims description 63
- 238000004513 sizing Methods 0.000 claims description 61
- 229920005989 resin Polymers 0.000 claims description 30
- 239000011347 resin Substances 0.000 claims description 30
- 229920000728 polyester Polymers 0.000 claims description 27
- 239000004814 polyurethane Substances 0.000 claims description 19
- 229920002635 polyurethane Polymers 0.000 claims description 19
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 18
- 239000011118 polyvinyl acetate Substances 0.000 claims description 18
- 239000011343 solid material Substances 0.000 claims description 18
- 239000000314 lubricant Substances 0.000 claims description 16
- 239000003795 chemical substances by application Substances 0.000 claims description 15
- 239000002131 composite material Substances 0.000 claims description 14
- 239000007822 coupling agent Substances 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 13
- 238000000465 moulding Methods 0.000 claims description 13
- 238000005507 spraying Methods 0.000 claims description 13
- -1 aromatic polyols Chemical class 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 11
- 150000004756 silanes Chemical class 0.000 claims description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 9
- 229910000077 silane Inorganic materials 0.000 claims description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 8
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 8
- 229920005862 polyol Polymers 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 230000003014 reinforcing effect Effects 0.000 claims description 7
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims description 7
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 6
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 claims description 6
- 239000000470 constituent Substances 0.000 claims description 6
- 150000003077 polyols Chemical class 0.000 claims description 6
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical group [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 5
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 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
- 150000008064 anhydrides Chemical class 0.000 claims description 4
- 239000002216 antistatic agent Substances 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 229920001187 thermosetting polymer Polymers 0.000 claims description 4
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 claims description 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 150000001767 cationic compounds Chemical class 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 2
- 239000003822 epoxy resin Substances 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 239000000194 fatty acid Substances 0.000 claims description 2
- 229930195729 fatty acid Natural products 0.000 claims description 2
- 150000004665 fatty acids Chemical class 0.000 claims description 2
- 150000002193 fatty amides Chemical class 0.000 claims description 2
- 239000001530 fumaric acid Substances 0.000 claims description 2
- 125000000524 functional group Chemical group 0.000 claims description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
- 125000005395 methacrylic acid group Chemical group 0.000 claims description 2
- 229920003986 novolac Polymers 0.000 claims description 2
- 229920001568 phenolic resin Polymers 0.000 claims description 2
- 239000005011 phenolic resin Substances 0.000 claims description 2
- 229920000058 polyacrylate Polymers 0.000 claims description 2
- 229920001515 polyalkylene glycol Polymers 0.000 claims description 2
- 229920000647 polyepoxide Polymers 0.000 claims description 2
- 229920001228 polyisocyanate Polymers 0.000 claims description 2
- 239000005056 polyisocyanate Substances 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 239000004634 thermosetting polymer Substances 0.000 claims description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
- 229920001567 vinyl ester resin Polymers 0.000 claims description 2
- 239000007787 solid Substances 0.000 description 24
- 239000000835 fiber Substances 0.000 description 21
- 238000002360 preparation method Methods 0.000 description 13
- 239000002585 base Substances 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 7
- 238000005520 cutting process Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000007921 spray Substances 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- NXQMCAOPTPLPRL-UHFFFAOYSA-N 2-(2-benzoyloxyethoxy)ethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCCOCCOC(=O)C1=CC=CC=C1 NXQMCAOPTPLPRL-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000004952 Polyamide Substances 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- UMVMVEZHMZTUHD-UHFFFAOYSA-N DL-Propylene glycol dibenzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C)COC(=O)C1=CC=CC=C1 UMVMVEZHMZTUHD-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 229910001651 emery Inorganic materials 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- YMHOBZXQZVXHBM-UHFFFAOYSA-N 2,5-dimethoxy-4-bromophenethylamine Chemical compound COC1=CC(CCN)=C(OC)C=C1Br YMHOBZXQZVXHBM-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 102100035861 Cytosolic 5'-nucleotidase 1A Human genes 0.000 description 1
- 101000802744 Homo sapiens Cytosolic 5'-nucleotidase 1A Proteins 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 241000545067 Venus Species 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- RLGQACBPNDBWTB-UHFFFAOYSA-N cetyltrimethylammonium ion Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)C RLGQACBPNDBWTB-UHFFFAOYSA-N 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- ARYZCSRUUPFYMY-UHFFFAOYSA-N methoxysilane Chemical compound CO[SiH3] ARYZCSRUUPFYMY-UHFFFAOYSA-N 0.000 description 1
- 239000006060 molten glass Substances 0.000 description 1
- KBJFYLLAMSZSOG-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)aniline Chemical compound CO[Si](OC)(OC)CCCNC1=CC=CC=C1 KBJFYLLAMSZSOG-UHFFFAOYSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229940068918 polyethylene glycol 400 Drugs 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical compound CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical class [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/24—Coatings containing organic materials
- C03C25/26—Macromolecular compounds or prepolymers
- C03C25/32—Macromolecular compounds or prepolymers obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
- C03C25/326—Polyureas; Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/24—Coatings containing organic materials
- C03C25/26—Macromolecular compounds or prepolymers
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/24—Coatings containing organic materials
- C03C25/26—Macromolecular compounds or prepolymers
- C03C25/32—Macromolecular compounds or prepolymers obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
- C03C25/323—Polyesters, e.g. alkyd resins
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/48—Coating with two or more coatings having different compositions
- C03C25/54—Combinations of one or more coatings containing organic materials only with one or more coatings containing inorganic materials only
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
- C08J5/06—Reinforcing macromolecular compounds with loose or coherent fibrous material using pretreated fibrous materials
- C08J5/08—Reinforcing macromolecular compounds with loose or coherent fibrous material using pretreated fibrous materials glass fibres
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Polymers & Plastics (AREA)
- Inorganic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Surface Treatment Of Glass Fibres Or Filaments (AREA)
- Reinforced Plastic Materials (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Ropes Or Cables (AREA)
Description
IN THE MATTER OF an Australian Application corresponding to PCT Application PCT/FR2004/050638 I, John Neil Albert SWEENEY BSc, PhD, Dip. Trans. IoL, translator to RWS Group Ltd, of Europa House, Marsham Way, Gerrards Cross, Buckinghamshire, England, do solemnly and sincerely declare that I am conversant with the English and French languages and am a competent translator thereof, and that to the best of my knowledge and belief the following is a true and correct translation of the PCT Application filed under No. PCT/FR2004/050638. Date: 4 July 2006 J. N. A. SWEENEY For and on behalf of RWS Group Ltd RAPID-IMPREGNATION SIZED GLASS STRANDS FOR THE REINFORCING OF POLYMERS The invention relates to glass strands coated with a 5 sizing composition which are intended for the reinforcing of organic materials of the polymer type. It also relates to the sizing composition used to coat said strands, to the composites incorporating these 10 strands and to the use of the sized strands in the manufacture of articles by molding. Glass strands used for reinforcing are generally produced industrially from streams of molten glass 15 flowing from the multiple orifices of a spinneret. These streams are drawn mechanically in the form of continuous filaments and are then gathered together into base strands, which are subsequently collected, for example by winding off on a rotating support. 20 Before they are gathered together, the filaments are coated with a sizing composition by passing over a suitable device, such as coating rolls. The sizing composition proves to be essential in 25 several respects. During the manufacture of the reinforcing strands, the sizing composition protects the glass filaments from the abrasion which occurs when the latter rub at high 30 speed over the various members which are used to guide them and to collect them. It also establishes bonds between the filaments, which makes it possible to give cohesion to the strand. As the strand is thus rendered more integral, it is easier to handle, in particular 35 during weaving operations, and untimely breakages are avoided. During the manufacture of composite materials, the sizing composition promotes the wetting and - 2 impregnation of the glass strands by the matrix to be reinforced, which matrix is generally employed in the form of a more or less fluid resin. The mechanical properties of the final composite are for this reason 5 markedly improved. The materials to be reinforced can combine with the glass strands in various forms: continuous or cut strands, mats of continuous or cut strands, fabrics, 10 and the like. The composites which incorporate cut glass strands can be obtained, inter alia, by the "contact molding" technique, which consists in coating the inside of an 15 open mold, without a countermold, with resin to be reinforced and glass strands of variable length. In the specific process of "molding by simultaneous spraying", the resin and the cut strands are sprayed together onto the inside walls of the mold by means of a "spray gun" 20 comprising an incorporated cutter capable of severing the strands drawn off from one or more wound packages, generally provided in the form of rovings, and of a device which makes it possible to atomize the resin, for example fed via a pneumatic pump. This simple and 25 adjustable process is particularly suited to the one off or short-run production of components based on thermosetting polymers belonging to the family of the polyesters or epoxides. 30 The quality of the composites obtained by this process depends largely on the properties introduced by the glass strands and thus on the size which coats them. The target is in particular to obtain compositions giving a size which can be easily wetted or impregnated 35 at the surface by the resin in order to provide close contact between the strands and the resin and to thus obtain the expected mechanical reinforcing properties. It is also desired for these compositions to be - 3 compatible with rapid processing, in particular for the strand/resin mixture which is sprayed onto the mold in the form of overlapping strips to be able to be spread out uniformly. The subsequent rolling stage, intended 5 to remove the air bubbles and to provide better distribution of the strands in the resin, should also be of short duration. Furthermore, it is necessary for the sizing composition 10 to have a degree of "incompatibility" with the resin, so as to prevent the strands/resin mixture from forming a compact mass which "collapses" by simple gravity. Nevertheless, the impregnation of the strand by the resin should be sufficiently fast so that the 15 strands/resin mixture can have a satisfactory "conformability", that is to say that it is capable of perfectly matching the shape of the mold. It is also necessary for the cut strands to retain 20 their integrity and not "to form filaments", namely for them not to burst, with the release of their constituent filaments, both during the cutting and spraying phase and during the rolling/debubbling operation. 25 It is thus seen that such compositions are difficult to develop as the targeted properties are rarely compatible with one another and that it is consequently necessary to make compromises. 30 One of the problems encountered during the implementation of the process for molding by simultaneous spraying of strands and of resin is the short lifetime of the blades with which the spray gun 35 is provided. Although they are made of hard steel, the blades of the cutter have a tendency to rapidly wear out on contact with the glass, which leads to "false cuts" and the formation of cut strands with a length greater than that desired. Depending upon the number of - 4 blades, their degree of wear and the position which they occupy on the cutter, it is possible to obtain a mixture of strands with a length corresponding to a whole multiple of the expected length. The false cuts 5 result in an unevenness in the carpet and in poor "conformability" of the cut strands/resin mixture in the mold. In addition, the need to have to replace the old blades at relatively short intervals also results in an increase in the cost of the components. 10 Sized glass strands suited to this type of molding, having an improved ability to be cut, are already known. 15 In FR-A-2 755 127, the strands are coated with a composition which comprises, in addition to adhesion agents capable of providing the sizing function, the combination of an aminosilane and of an unsaturated silane. 20 In WO-A-02/059055, the sizing composition coating the glass strands combines at least one bissilane and at least one unsaturated monosilane chosen from vinylsilanes and (meth)acrylosilanes. 25 There exists a need to have available a sizing composition which makes it possible to meet current productivity standards, which require having available strands which can be rapidly impregnated by the resin, 30 without, however, affecting the other properties of the strand, and which exhibit a high ability to be cut, making it possible to increase the longevity of the cutting blades while producing the least possible amount of short fibers. 35 The aim of the present invention is thus to provide a sizing composition for reinforcing strands, which are intended in particular for open mold molding and more particular for molding by simultaneous spraying of - 5 glass strands and of resin, which makes it possible to have rapid impregnation of the strands by the resin and an improved ability to be cut with limited production of short fibers. 5 A subject-matter of the invention is glass strands coated with an aqueous composition which combines, as film-forming adhesion agents, at least one polyester, at least one polyvinyl acetate and at least one 10 polyurethame. In the present invention, the term "glass strands coated with a sizing composition" is understood to mean glass strands "which have been coated with a sizing 15 composition which comprises ... ", that is to say not only glass strands coated with the composition in question as they are obtained at the immediate outlet of the sizing member or members but also these same strands after they have been subjected to one or more 20 other treatments. Mention may be made, as examples of such treatments, of the drying operations targeted at removing the solvent from the composition and the treatments resulting in the polymerization/crosslinking of some constituents of the sizing composition. 25 Still within the context of the invention, the term "strands" should be understood as meaning the base strands resulting from the gathering together under the spinneret of a multitude of filaments and the products 30 derived from these strands, in particular the assemblages of these base strands into rovings. Such assemblages can be obtained by simultaneously reeling off several wound base strand packages and by then gathering them together into slivers which are wound 35 off onto a rotating support. It can also be "direct" rovings with a count (or mass length) equivalent to that of the assembled rovings obtained by gathering together filaments directly under the spinneret and winding onto a rotating support.
- 6 Still according to the invention, the term "aqueous sizing composition" is understood to mean a sizing composition in the form of a solution in which the 5 liquid phase is composed to 97% by weight of water, preferably 99% and better still 100%, the remainder being composed, if appropriate, of one or more essentially organic solvents which can help in dissolving some constituents of the sizing composition. 10 In accordance with the invention, the sizing composition comprises, as film-forming adhesion agents, the blend of at least one polyester, of at least one polyvinyl acetate and of at least one polyurethane. 15 The polyester makes it possible to obtain rapid impregnation by the resin and good conformability of the strands/resin mixture in the mold. It also confers stiffness on the glass strands. 20 The polyester is obtained by reaction of polycarboxylic acid(s) and/or of anhydride(s) of these acids and of polyol(s). 25 Preferably, the acid is chosen from saturated, unsaturated or aromatic diacids, such as fumaric acid, isophthalic acid and terephthalic acid, the anhydride is chosen from phthalic anhydride and maleic anhydride, and the polyol is chosen from polyalkylene glycols, 30 such as ethylene glycol and propylene glycol, aromatic polyols, such as bisphenol A or F, and novolaks. Preference is given to the polyesters obtained by reaction of phthalic or maleic anhydride and of 35 bisphenol A or F, and of phthalic and maleic anhydrides and of propylene glycol. Generally, the polyester exhibits a molecular weight which varies from 4000 to 17 000 g/mol.
- 7 The amount of polyester generally represents 50 to 80% of the solid materials of the composition, preferably 50 to 70%. 5 The polyvinyl acetate is important in achieving the required level of cutting. The molecular weight of the polyvinyl acetate is 10 generally less than 80 000 g/mol, preferably less than 70 000 g/mol and better still it is between 40 000 and 65 000 g/mol. The amount of polyvinyl acetate used generally 15 represents 10 to 40% by weight of the solid materials of the sizing composition, preferably 20 to 30%. When the amount represents less than 10% of the solid materials, the ability to be cut is not satisfactory and, when it exceeds 40%, the impregnation of the 20 strands is inadequate. The polyurethane renders the strand more integral and improves its ability to be cut. It also acts as a lubricant. 25 The polyurethane is chosen from the polyurethanes resulting from the reaction of at least one polyisocyanate and of at least one polyol comprising an aliphatic and/or cycloaliphatic chain. 30 Preferably, the polyurethane has a molecular weight of less than 20 000 g/mol, preferably of between 4000 and 15 000 g/mol. 35 The amount of polyurethane used generally represents 8 to 15% by weight of the solid materials of the sizing composition, preferably 8 to 10%. Preferably, the sum of the contents by weight of - 8 polyester, of polyvinyl acetate and of polyurethane represents at least 90%, preferably at least 95%, of the solid materials of the sizing composition. 5 In addition to the abovementioned components which participate essentially in the structure of the size, the sizing composition can advantageously comprise one or more other components (hereinafter denoted as "additives"). The sizing composition can thus comprise 10 a lubricating agent in an amount which can represent up to 5% by weight of the solid materials of the sizing composition. In addition to this role of protecting the filaments 15 from mechanical abrasion, the lubricant contributes to limiting the formation of short fibers, to increasing the stiffness of the strand and to preventing adhesive bonding of the wraps on the wound base strand packages. 20 Generally, this agent is chosen from cationic compounds of the polyalkyleneimide type and nonionic compounds of the esters of fatty acids and of poly(alkylene glycol)s/poly(oxyalkylene) type, such as polyethylene glycol monolaurate, or of the poly(oxyalkylenated) 25 fatty amides type, such as polyoxyethylenated hydrogenated tallow amides. The sizing composition can also comprise at least one coupling agent which makes it possible to attach the 30 size to the surface of the glass filaments. The coupling agent is generally chosen from silanes, such as y-glycidoxypropyltrimethoxysilane, y-acryloyloxy propyltrimethoxysilane, y-methacryloyloxypropyltri methoxysilane, poly(oxyethylene/oxypropylene)tri 35 methoxysilane, y-aminopropyltriethoxysilane, vinyl trimethoxysilane, phenylaminopropyltrimethoxysilane or styrylaminoethylaminopropyltrimethoxysilane, siloxanes, titanates, zirconates, in particular of aluminum, and mixtures of these compounds. Preferably, silanes are - 9 chosen. Advantageously, the composition comprises at least two coupling agents, at least one of which is an 5 unsaturated silane and the other of which is an aminosilane. A particularly advantageous combination comprises at least one silane including an acrylic or methacrylic functional group and an aminosilane chosen from bis(y-trimethoxysilylpropyl)silane and bis(y 10 triethoxysilylpropyl)silane. In particular, by adjusting the ratio by weight of the unsaturated silane to the aminosilane, it is possible to regulate tha amount of "oversize" to be applied to the base strands, as is indicated later. The ratio generally varies from 15 1:1.5 to 1:6, preferably from 1:2 to 1:5. The higher the ratio, the lower the amount of oversize to be deposited. The amount of coupling agent generally varies from 1 to 20 6% by weight of the solid materials of the sizing composition, is preferably greater than 1.5% and is generally of the order of 2%. It is also possible to introduce, as additive, an 25 antistatic agent, such as lithium chloride, in an amount representing less than 5% by weight of the solid materials of the sizing composition. The glass strands coated with the sizing composition in 30 accordance with the invention exhibit a loss on ignition of less than 2.2%, preferably of greater than 1% and better still of between 1.0 and 1.45%. Generally, the glass strands in accordance with the 35 invention are provided in the form of wound base strand packages which are subjected to a heat treatment. This treatment is intended essentially to remove the water introduced by the sizing composition and, if appropriate, makes it possible to accelerate the - 10 crosslinking of the film-forming adhesion agents. The conditions of the treatment can vary according to the weight of the wound package. The drying is generally carried out at a temperature of the order of 110 to 5 140oC for several hours, preferably 12 to 18 hours. As has already been said, the base strands thus obtained are generally removed from the wound package and combined with several other base strands into a 10 sliver which is subsequently wound onto a rotating support to form a roving. The "oversize" application of a composition including a cationic antistatic agent of the quaternary ammonium salt type to the strands makes it possible to reinforce the ability of the strands to 15 be cut. Consequently, the deposition of the abovementioned composition on the base strands, after removing from the wound package and gathering together to form the sliver, contributes to improving the ability to be cut and consequently increases the 20 lifetime of the blades. The strands are preferably coated with an aqueous composition comprising 20 to 35% by weight of cetyltrimethylammonium chloride, preferably of the order of 25% by weight. 25 The amount of "oversize" deposited generally represents 0.02 to 0.2% by weight of the strand, preferably 0.05 to 0.10%. The strands coated with the sizing composition 30 according to the invention can be composed of glass of any nature provided that it is capable of being fiberized, for example of E, C or AR (alkali-resistant) glass or glass with a low level of boron (less than 5%). E glass and glass with a low level of boron are 35 preferred. These same strands are composed of filaments with a diameter which can vary within a wide range, for example 9 to 17 pm, preferably 11 to 13 p.m.
- 11 The strands advantageously have a count of between 30 and 160 tex, preferably 40 and 60 tex. Such cut glass strands are evenly and homogeneously distributed within the resin, which makes it possible to have 5 reinforcement of excellent quality. Another subject-matter of the invention is the sizing composition capable of coating said glass strands, which composition is characterized in that it comprises 10 an aqueous blend of at least one polyester, of at least one polyvinyl acetate and of at least one polyurethane as are defined above. The sizing composition is an aqueous blend comprising 15 the constituents below in the following contents by weight, expressed as percentages of the solid materials: * 50 to 80% of at least one polyester, preferably 50 to 70%, 20 * 10 to 40% of at least one polyvinyl acetate, preferably 20 to 30%, * 8 to 15% of at least one polyurethane, preferably 8 to 10%, * 0 to 5% of at least one lubricating agent, 25 * 1 to 6% of at least one coupling agent, preferably equal to or greater than 1.5%. Advantageously, the sizing composition comprises between 5 and 15% by weight of solid materials, 30 preferably between 6 and 11%. Advantageously, the liquid phase is composed to 100% of water. Another subject-matter of the invention is also the composites comprising the glass strands coated with the 35 sizing composition. Such composites comprise at least one thermosetting material, preferably a polyester, a vinyl ester, an acrylic polymer, a phenolic resin or an epoxy resin, and glass strands composed, in all or part, of glass strands in accordance with the - 12 invention. The level of glass within the composite is generally between 20 and 45% by weight and preferably between 25 5 and 35%. In addition to their advantages related to the processing by molding (rapid rate of impregnation and good ability to be cut, combined with the limited 10 formation of short fibers), the glass strands confer, on the composites which include them, better resistance to aging, in particular in a moist environment. A further subject matter of the invention is the use of 15 the glass strands coated with the sizing composition for the production of components by the open mold molding technique, in particular by simultaneous spraying of said strands and of resin. 20 Another subject matter of the invention is the use of said glass strands for the production of pipes by the centrifuging technique, which consists in simultaneously spraying the strands and a resin into a rotating mold, the impregnation of the strands being 25 carried out by virtue of the centrifugal force. The following examples make it possible to illustrate the invention without, however, limiting it. 30 EXAMPLE 1 (COMPARATIVE) A sizing composition is prepared in the form of an aqueous solution comprising, as % by weight of the solid materials: 35 * film-forming adhesion agents - polyvinyl acetate(); molecular weight 50 000 60.1 - vinyl acetate/N-methylolacrylamide copolymer (2) 21.9 - 13 * coupling agents - diaminosilane (3) 1.3 - vinyltriethoxysilane (4) 2.1 * plasticizer 5 - mixture of diethylene glycol dibenzoate and of propylene glycol dibenzoate
(
5 ) (50:50 ratio by weight) 9.8 * lubricants - polyethylene glycol 400 monolaurate (6) 4.1 10 - polyethyleneimide comprising free amide functional groups(7) 0.7 * water: amount sufficient to give 100 ml of sizing composition. 15 The sizing composition is prepared in the following way: The alkoxy groups of the silane( 3 ) and silane( 4 are hydrolyzed by addition of acid to an aqueous solution 20 of this silane kept stirred. The other constituents are subsequently introduced, still with stirring, and the pH is adjusted to a value of 4 + 0.2, if necessary. 25 The sizing composition is used to coat, in a known way, filaments of E glass with a diameter of approximately 12 pm drawn from glass streams flowing from the orifices of a spinneret, the filaments subsequently 30 being gathered together in the form of wound base strand packages with a count equal to 60 tex. The wound package is dried at 130 0 C for 12 hours. 35 The base strands extracted from 7 wound packages are coated with an aqueous solution comprising 25% by weight of cetyltrimethylammonium chloride (amount deposited on a dry basis: 0.05%).
- 14 The strand unwound from the roving is inserted into a cutting device comprising two blades, one made of hard steel and the other made of rapidly wearing "soft" steel (heat treatment at 5500C), and equipped with 5 strength and temperature sensors. The cutting, carried out at 200C under a relative humidity of 50%, is adjusted in order to form cut strands with a length of 50 mm. The ability to be cut is measured by the weight of the glass strands which can be cut until the 10 appearance of strands with twice the length (2 x 50 mm). The value 1 is assigned to the weight of cut strands obtained, which value is used here as reference value for measuring the ability to be cut. 15 EXAMPLE 2 The preparation is carried out under the conditions of example 1, modified in that the sizing composition comprises, as % by weight of the solid materials: 20 * film-forming adhesion agents - polyester (8) 60.5 - polyvinyl acetate
(
"
) 22.5 - polyurethane (9) 10.0 * coupling agents 25 - (y-methacryloyloxypropyl)triethoxysilane (0 ) 3.2 * lubricating agent - polyethyleneimide polyamide salt"" 0.8 - quaternary ammonium derivative (12) 3.0 * water: amount sufficient to give 100 ml of 30 sizing composition. The sizing composition has a solids content of 6.6%. The following properties are evaluated on the strand 35 resulting from the roving: - the loss on ignition, in %, is measured under the conditions of standard ISO 1887, - the short fibers are measured by reeling off the strand over a device composed of 6 tension rollers, - 15 at the rate of 93 m/min. The device is placed in a conditioned room at 20 0 C and 50% relative humidity. The short fibers are defined by the amount of fibrils, in mg, obtained after reeling off a weight 5 of strand of 1 kg. The values of the loss on ignition, of the short fibers and of the ability to be cut appear in table 1. 10 EXAMPLE 3 The preparation is carried out under the conditions of example 2, modified in that the content of cetyltrimethylammonium chloride deposited on the base 15 strands is equal to 0.10%. The composition has a solids content of 6.6%. The values of the loss on ignition, of the short fibers 20 and of the ability to be cut appear in table 1. EXAMPLE 4 (COMPARATIVE) The preparation is carried out under the conditions of 25 example 2, modified in that the film-forming adhesion agents are composed solely of polyester(8) in a content of 93%. The sizing composition has a solids content of 6.5%. 30 The values of the loss on ignition, of the short fibers and of the ability to be cut appear in table 1. EXAMPLE 5 (COMPARATIVE) 35 The preparation is carried out under the conditions of example 2, modified in that the sizing composition comprises the following film-forming adhesion agents, as % by weight of the solid materials: - 16 * film-forming adhesion agents - polyester (8) 88.4 - polyurethane (9) 4.8 * coupling agents 5 - (y-methacryloyloxypropyl)triethoxysilane
(
"
0 ) 3.1 * lubricating agent - polyethyleneimide polyamide salt" (11) 0.8 - quaternary ammonium derivative (12 ) 2.9 * water: amount sufficient to give 100 ml of 10 sizing composition. The sizing composition has a solids content of 6.8%. The values of the loss on ignition, of the short fibers 15 and of the ability to be cut appear in table 1. EXAMPLE 6 (COMPARATIVE) The preparation is carried out under the conditions of 20 example 2, modified in that the sizing composition comprises the following film-forming adhesion agents, as % by weight of the solid materials: * film-forming adhesion agents - polyester 8 ) 59.2 25 - polyvinyl acetate
(
"
) 29.6 * coupling agents - (y-methacryloyloxypropyl)triethoxysilane (° 0 ) 3.1 * plasticizer - mixture of diethylene glycol dibenzoate 30 and of propylene glycol dibenzoate ( 5 ) (50:50 ratio by weight) 4.4 * lubricating agent - polyethyleneimide polyamide salt (11 ) 0.8 - quaternary ammonium derivative (12) 2.9 35 The sizing composition has a solids content of 6.8%. The values of the loss on ignition, of the short fibers and of the ability to be cut appear in table 1.
- 17 EXAMPLE 7 (COMPARATIVE) Use is made of glass strands coated with a size which 5 are suitable for the preparation of composite components by molding by simultaneously spraying. These strands are sold by PPG under the reference 6313. The values of the loss on ignition, of the short fibers 10 and of the ability to be cut appear in table 1. EXAMPLE 8 The preparation is carried out under the conditions of 15 example 2, modified in that the sizing composition comprises 0.2% of lubricating agent
(
"
) and is devoid of (12) antistatic agent 2 The sizing composition has a solids content of 6.4%. 20 The values of the loss on ignition, of the short fibers and of the ability to be cut appear in table 1. EXAMPLE 9 25 The preparation is carried out under the conditions of example 3, modified in that the sizing composition comprises 0.2% of lubricating agent(11 30 The sizing composition has a solids content of 6.94%. The values of the loss on ignition, of the short fibers and of the ability to be cut appear in table 1. EXAMPLE 10 35 The preparation is carried out under the conditions of example 2, modified in that the sizing composition comprises, as % by weight of the solid materials: - 18 - polyester (8) 54.0 - polyvinyl acetate(1) 24.0 - polyurethane (9) 10.0 - silane ( 10 ) 1.7 5 - lubricating agent ( 1
"
) 0.3 The sizing composition has a solids content of 8.4%. The values of the loss on ignition, of the short fibers 10 and of the ability to be cut appear in table 1. EXAMPLE 11 The preparation is carried out under the conditions of 15 example 2, modified in that, in the sizing composition, the polyester(8) is replaced by the polyester(13) The sizing composition has a solids content of 8.3%. 20 The values of the loss on ignition, of the short fibers and of the ability to be cut appear in table 1. EXAMPLE 12 25 The preparation is carried out under the conditions of example 2, modified in that the sizing composition comprises the following coupling agents, as % by weight of the solid materials: - polyester ( 8 ) 61.8 30 - polyvinyl acetate
(
"
) 23.0 - polyurethane (9) 10.2 - unsaturated silane ( 10 ) 0.8 - bis(triethoxysilylpropyl)amine "' 4.0 - lubricating agent
(
"
) 0.2 35 The sizing composition has a solids content of 8.6%. The values of the loss on ignition, of the short fibers and of the ability to be cut appear in table 1.
- 19 EXAMPLE 13 The preparation is carried out under the conditions of 5 example 12, modified in that the content of cetyltrimethylammonium chloride deposited on the base strands is equal to 0.10%. The ability to be cut is given in table 1. 10 EXAMPLE 14 The preparation is carried out under the conditions of example 12, modified in that cetyltrimethylammonium 15 chloride is not deposited on the base strands. The values of the loss on ignition, of the short fibers and of the ability to be cut appear in table 1. 20 EXAMPLES 15 TO 17 The strands obtained according to examples 2 and 10 (examples 15 and 16) and according to comparative example 7 (example 17) are used to manufacture 25 composite components by the technique of molding by simultaneous spraying under the following conditions: - the glass strand removed from the roving is introduced into a spray gun (Venus from Matrasur) which makes it possible to cut it and to spray it 30 simultaneously with an unsaturated polyester resin (Enydyne D5O 4500 TY, sold by Cray Valley) with a viscosity equal to 4.5 dPa-s at 25 0 C, with high reactivity and thixotropic, - the mold into which the cut strands and the resin 35 are sprayed is a mold in the form of a staircase which comprises a vertical wall with a height of 1 m, then a stair with a depth of 0.20 m and a height of 0.2 m, and finally a horizontal wall with a length of 1 m. The horizontal wall - 20 comprises two grooves with a depth of 2 cm which make it possible to evaluate the conformation of the cut strands/resin mixture, - the mixture sprayed onto the mold includes 30% by 5 weight of glass and has a mean thickness of the order of 3 mm. The performances of the cut strands/resin mixture are evaluated for the following parameters: 10 - evenness of the carpet - vertical wall strength - rate of impregnation of the cut strands by the resin. 15 The evaluation relating to these parameters is measured visually according to the following scale of values: 1 = very bad; 2 = bad; 3 = fairly good; 4 = good and 5 = very good. 20 The performances of the strands are collated in table 2 below: Table 2 Ex. 15 Ex. 16 Ex. 17 Strand Ex. 2 Ex. 10 Ex. 7 Dispersion of the carpet 4.5 4 3.5 Vertical wall strength 2.5 4.5 2 Rate of impregnation 4 4 4 25 On reading the table, it is found that the strands according to the invention (examples 2 and 3), which combine a polyester, a polyvinyl acetate and a polyurethane as film-forming adhesion agents, exhibit a 30 better ability to be cut than the strands comprising only one or two of these agents (examples 4 to 6), at an equivalent loss on ignition. The amount of short fibers formed is low, of the same level as for examples 4 to 6 and much lower than that of the strands of - 21 example 7. The ability to be cut is improved when the content of "oversize" is greater (example 3). 5 The strands having lower contents of lubricating agent (examples 8 and 9) and of coupling agent (example 10) have a high ability to be cut and moderate production of short fibers. 10 The combination of an unsaturated silane and of an aminosilane makes it possible to obtain strands having a high ability to be cut without oversize (example 14), this ability greatly increasing when the content of 15 oversize increases (examples 12 and 13). Table 2 shows that the strands according to the invention (examples 15 to 17) retain a high rate of impregnation under the conditions of the spraying, 20 equivalent to that of the strands of comparative example 7, with, however, an improved vertical wall strength and evenness of the carpet. These strands obtained in the context of the invention 25 exhibit an excellent compromise between the ability to be cut, the production of short fibers and the conditions of molding by simultaneous spraying of resin. 30 EXAMPLES 18 AND 19 The ability of the strand according to example 10 (example 18) to be used to manufacture pipes by the centrifuging technique by simultaneous spraying of cut 35 strands and of resin into a rotating mold is evaluated by comparison with a known strand suitable for this use (sold by PPG under the reference 6428; example 20). The integrity of the strand is measured under the - 22 following conditions: the strand reeled off from a roving is introduced into a Wolfangel 500 cutter, which cuts it and sprays it substantially horizontally onto a vertical wall (cutting rate: 600 m/min; length: 12 mm). 5 The integrity of the cut strand is determined visually according to a scale of values ranging from 1 (bad; fluffy appearance) to 5 (very good; no rupturing of the strand). 10 The ability to be cut is measured under the conditions of example 1. Example 19 Example 20 Integrity 4.5 4.5 Ability to be cut 2.40 0.95 The strand according to the invention exhibits a 15 markedly improved ability to be cut in comparison with the known strand and an identical integrity. (1) Sold under the reference "Vinamul 8852" by VINAMUL; solids content: 55% 20 (2) Sold under the reference "Vinamul 8828" by VINAMUL; solids content: 52% (3) Sold under the reference "Silquest A 1126" by GESM; solids content: 35% (4) Sold under the reference "Silquest A 151" by GESM; solids content: 98% (5) Sold under the reference "K-Flex 500" by NOVEON; solids content: 100% (6) Sold under the reference "Ensital 4L" by COGNIS; solids content: 100% 25 (7) Sold under the reference "Emery 6717" by COGNIS; solids content: 100% (8) Sold under the reference "Neoxil 954D" by DSM; solids content: 47% (9) Sold under the reference "Neoxil 9851" by DSM; solids content: 33% (10) Sold under the reference "Silquest A 174" by GESM; solids content: 70% (11) Sold under the reference "Emery 6760" by COGNIS; solids content: 100% 30 (12) Sold under the reference "Neoxil AO 5620" by DSM; solids content: 100% (13) Sold under the reference "Filco 350" by COIM; solids content: 45% (14) Sold under the reference "A 1122" by DEGUSSA; solids content: 98% (N Lfl H CN HH I I CN H 0 HD C') 0 H H CN I N Hn 0 U H 0 0 C 0 H 0 0 Cl En
Claims (25)
1. A glass strand coated with an aqueous sizing composition, characterized in that said composition 5 comprises, as film-forming adhesion agents, at least one polyester, at least one polyvinyl acetate and at least one polyurethane.
2. The glass strand as claimed in claim 1, 10 characterized in that the polyester has a molecular weight varying from 4000 to 17 000 g/mol.
3. The glass strand as claimed in claim 1 or 2, characterized in that the polyester is obtained by 15 reaction of polycarboxylic acid(s) and/or of anhydride(s) of these acids and of polyol(s).
4. The glass strand as claimed in claim 3, characterized in that the acid is chosen from 20 saturated, unsaturated or aromatic diacids, such as fumaric acid, isophthalic acid and terephthalic acid, the anhydride is chosen from phthalic anhydride and maleic anhydride, and the polyol is chosen from polyalkylene glycols, such as ethylene glycol and 25 propylene glycol, aromatic polyols, such as bisphenol A or F, and novolaks.
5. The glass strand as claimed in one of claims 1 to 4, characterized in that the polyvinyl acetate has a 30 molecular weight of less than 80 000 g/mol, preferably of less than 70 000 g/mol.
6. The glass strand as claimed in one of claims 1 to 5, characterized in that the polyurethane results from 35 the reaction of at least one polyisocyanate and of at least one polyol comprising an aliphatic and/or cycloaliphatic chain.
7. The glass strand as claimed in one of claims 1 to - 25 6, characterized in that the polyurethane has a molecular weight of less than 20 000 g/mol, preferably of between 4000 and 15 000 g/mol. 5
8. The glass strand as claimed in one of claims 1 to 7, characterized in that the composition additionally comprises a lubricating agent.
9. The glass strand as claimed in claim 8, 10 characterized in that the lubricating agent is chosen from cationic compounds of the polyalkyleneimide type and nonionic compounds of the esters of fatty acids and of poly(alkylene glycol)/poly(oxyalkylene) type or of the poly(oxyalkylenated) fatty amides type. 15
10. The glass strand as claimed in one of claims 1 to 9, characterized in that the composition additionally comprises a coupling agent chosen from silanes, siloxanes, titanates, zirconates and mixtures of these 20 compounds.
11. The glass strand as claimed in claim 10, characterized in that the coupling agent comprises an unsaturated silane and an aminosilane. 25
12. The glass strand as claimed in claim 11, characterized in that the unsaturated silane includes at least one acrylic or methacrylic functional group and the aminosilane is bis(y-trimethoxysilylpropyl) 30 silane or bis(y-triethoxysilylpropyl)silane.
13. The glass strand as claimed in one of claims 1 to 12, characterized in that it exhibits a loss on ignition of less than 2.2%, preferably of greater than 35 1%.
14. The glass strand as claimed in one of claims 1 to 13, characterized in that it is composed of filaments with a diameter varying from 9 to 17 pm. - 26
15. The glass strand as claimed in one of claims 1 to 14, characterized in that it exhibits a count of between 30 and 160 tex, preferably 40 and 60 tex. 5
16. The glass strand as claimed in one of claims 1 to 15, characterized in that it additionally comprises an oversize including an antistatic agent of the quaternary ammonium salt type. 10
17. The glass strand as claimed in claim 16, characterized in that the quaternary ammonium salt is cetyltrimethylammonium chloride.
18. A sizing composition intended to coat glass 15 strands as claimed in one of claims 1 to 17, characterized in that it comprises an aqueous blend of at least one polyester, of at least one polyvinyl acetate and of at least one polyurethane. 20
19. The composition as claimed in claim 18, characterized in that it comprises the constituents below in the following contents by weight, expressed as percentages of the solid materials: * 50 to 80% of at least one polyester, preferably 50 to 25 70%, * 10 to 40% of at least one polyvinyl acetate, preferably 20 to 30%, * 8 to 15% of at least one polyurethane, preferably 8 to 10%, 30 * 0 to 5% of at least one lubricating agent, * 1 to 6% of at least one coupling agent, preferably equal to or greater than 1.5%.
20. The composition as claimed in claim 18 or 19, 35 characterized in that it comprises 5 to 15% by weight of solid materials, preferably 6 to 11%.
21. A composite comprising at least one thermosetting polymer material and reinforcing glass strands, - 27 characterized in that all or part of the strands are composed of strands as claimed in one of claims 1 to 17. 5
22. The composite as claimed in claim 21, characterized in that the thermosetting material is a polyester, a vinyl ester, an acrylic polymer, a phenolic resin or an epoxy resin. 10
23. The composite as claimed in claim 21 or 22, characterized in that it comprises 20 to 45% by weight of glass.
24. The use of the glass strands as claimed in one of 15 claims 1 to 17 in the production of components by the open mold molding technique, in particular by simultaneous spraying of said strands and of resin.
25. The use of the glass strands as claimed in one of 20 claims 1 to 17 in the production of pipes by the centrifuging technique by simultaneous spraying of said strands and of resin.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0314802A FR2864073B1 (en) | 2003-12-17 | 2003-12-17 | QUICK-IMPREGNATED ENSIMES GLASS YARNS FOR REINFORCING POLYMERIC MATERIALS |
| FR0314802 | 2003-12-17 | ||
| PCT/FR2004/050638 WO2005058771A2 (en) | 2003-12-17 | 2004-12-02 | Sized glass fibres with fast impregnation for the reinforcement of polymer materials |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2004299305A1 true AU2004299305A1 (en) | 2005-06-30 |
| AU2004299305B2 AU2004299305B2 (en) | 2010-08-19 |
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ID=34630245
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2004299305A Ceased AU2004299305B2 (en) | 2003-12-17 | 2004-12-02 | Sized glass fibres with fast impregnation for the reinforcement of polymer materials |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20070148453A1 (en) |
| EP (1) | EP1697270A2 (en) |
| JP (1) | JP4977857B2 (en) |
| CN (1) | CN1918081B (en) |
| AU (1) | AU2004299305B2 (en) |
| BR (1) | BRPI0417705A (en) |
| FR (1) | FR2864073B1 (en) |
| RU (1) | RU2006125410A (en) |
| WO (1) | WO2005058771A2 (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070059506A1 (en) * | 2005-09-12 | 2007-03-15 | Hager William G | Glass fiber bundles for mat applications and methods of making the same |
| US20070057404A1 (en) * | 2005-09-12 | 2007-03-15 | Hager William G | Compression and injection molding applications utilizing glass fiber bundles |
| JP5702659B2 (en) * | 2010-08-05 | 2015-04-15 | 積水化学工業株式会社 | Manufacturing method of multi-layer pipe with flange and multi-layer pipe with flange |
| PL2631337T3 (en) * | 2012-02-24 | 2015-12-31 | Ems Patent Ag | Fibre-resin composite material and method for producing the same |
| CN103160235B (en) * | 2012-04-17 | 2014-10-29 | 南京彤天广元高分子材料有限公司 | Resin powder bonding agent |
| MX2018004178A (en) * | 2015-10-08 | 2018-06-20 | Ocv Intellectual Capital Llc | Post-coating composition for reinforcement fibers. |
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| CN106431014A (en) * | 2016-08-28 | 2017-02-22 | 山东玻纤集团股份有限公司 | Glass fiber impregnating compound for woven roving and preparation method of glass fiber impregnating compound |
| CN106348624A (en) * | 2016-08-29 | 2017-01-25 | 山东玻纤集团股份有限公司 | Impregnating compound for spraying glass fiber and preparing method thereof |
| CN106587659B (en) * | 2016-11-04 | 2019-05-21 | 巨石集团有限公司 | A kind of glass fiber infiltration agent and application thereof |
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| US4137209A (en) * | 1977-11-14 | 1979-01-30 | Owens-Corning Fiberglas Corporation | Glass fiber size composition |
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| US4370439A (en) * | 1979-03-22 | 1983-01-25 | Ppg Industries, Inc. | Method of preparing a sizing composition for treating glass fibers |
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| US4789593A (en) * | 1985-06-25 | 1988-12-06 | Ppg Industries, Inc. | Glass fibers with fast wettability and method of producing same |
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| US5247004A (en) * | 1989-02-03 | 1993-09-21 | Ppg Industries, Inc. | Polymeric-containing compositions with improved oxidative stability |
| US5219656A (en) * | 1991-07-12 | 1993-06-15 | Ppg Industries Inc. | Chemically treated glass fibers for reinforcing polymeric materials |
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| DE69402882T2 (en) * | 1993-09-27 | 1997-09-11 | Ppg Industries, Inc., Pittsburgh, Pa. | FIBERGLASS FINISHING COMPOSITIONS, COATED GLASS FIBERS AND METHOD FOR USE THEREOF |
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| DE19523512A1 (en) * | 1995-06-28 | 1997-01-02 | Bayer Ag | Sizing composition, sized glass fibers and their use |
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| FR2826359B1 (en) * | 2001-06-21 | 2004-05-07 | Saint Gobain Vetrotex | SIZED GLASS WIRES, SIZING COMPOSITION AND COMPOSITES COMPRISING SAID WIRES |
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| JP4370140B2 (en) * | 2003-09-30 | 2009-11-25 | オーウェンスコーニング製造株式会社 | Glass fiber sizing agent for reinforcing fiber reinforced unsaturated polyester resin, |
-
2003
- 2003-12-17 FR FR0314802A patent/FR2864073B1/en not_active Expired - Fee Related
-
2004
- 2004-12-02 WO PCT/FR2004/050638 patent/WO2005058771A2/en not_active Ceased
- 2004-12-02 US US10/583,560 patent/US20070148453A1/en not_active Abandoned
- 2004-12-02 RU RU2006125410/04A patent/RU2006125410A/en not_active Application Discontinuation
- 2004-12-02 CN CN2004800417936A patent/CN1918081B/en not_active Expired - Fee Related
- 2004-12-02 BR BRPI0417705-3A patent/BRPI0417705A/en not_active IP Right Cessation
- 2004-12-02 JP JP2006544510A patent/JP4977857B2/en not_active Expired - Fee Related
- 2004-12-02 AU AU2004299305A patent/AU2004299305B2/en not_active Ceased
- 2004-12-02 EP EP04816500A patent/EP1697270A2/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| CN1918081A (en) | 2007-02-21 |
| BRPI0417705A (en) | 2007-03-20 |
| EP1697270A2 (en) | 2006-09-06 |
| CN1918081B (en) | 2012-04-11 |
| FR2864073A1 (en) | 2005-06-24 |
| JP4977857B2 (en) | 2012-07-18 |
| US20070148453A1 (en) | 2007-06-28 |
| JP2007514633A (en) | 2007-06-07 |
| FR2864073B1 (en) | 2006-03-31 |
| WO2005058771A3 (en) | 2006-02-09 |
| AU2004299305B2 (en) | 2010-08-19 |
| WO2005058771A2 (en) | 2005-06-30 |
| RU2006125410A (en) | 2008-01-27 |
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