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EP0534981A1 - Composition d'encollage pour l'impregnation de filaments orientes - Google Patents

Composition d'encollage pour l'impregnation de filaments orientes

Info

Publication number
EP0534981A1
EP0534981A1 EP91908021A EP91908021A EP0534981A1 EP 0534981 A1 EP0534981 A1 EP 0534981A1 EP 91908021 A EP91908021 A EP 91908021A EP 91908021 A EP91908021 A EP 91908021A EP 0534981 A1 EP0534981 A1 EP 0534981A1
Authority
EP
European Patent Office
Prior art keywords
thermoplastic
slurry
glass fiber
fiber
impregnated
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP91908021A
Other languages
German (de)
English (en)
Inventor
Jean-Claude Pollet
Gary Lynn Williams
Gordon Patrick Armstrong
Martin Charles Flautt
David Lee Shipp
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Owens Corning
Original Assignee
Owens Corning Fiberglas Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Owens Corning Fiberglas Corp filed Critical Owens Corning Fiberglas Corp
Publication of EP0534981A1 publication Critical patent/EP0534981A1/fr
Withdrawn legal-status Critical Current

Links

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
    • 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
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
    • C08L81/02—Polythioethers; Polythioether-ethers

Definitions

  • This invention relates to a size composition useful for impregnating a highly loaded, impregnated fibrous strand where the impregnation takes place during the fiber forming operation.
  • this invention relates to a thermoplastic powder impregnated glass fiber strand.
  • Sizing compositions typically employed as coatings for glass fibers have conventionally been applied to the surface of the glass fibers after the glass fiber has been formed. Typically it is necessary to first produce the glass fibers by providing a thin layer of a size composition to the surface of the bare glass fibers.
  • the size composition must be compatible with the glass fiber and the resin which Is subsequently applied to the sized fiber.
  • the size composition serves to improve the bonding relationship between the glass fibers and the polymeric or thermoplastic resins.
  • the glass fibers are then collected into a strand and the strand is wound around a take-up bobbin to form a substantially cylindrical package, conventionally termed a "yarn package".
  • the yarn package is then air dried or subjected to elevated temperatures in order to dry the size composition applied to the surface of the glass fibers.
  • the glass fibers are thereafter impregnated with the thermoplastic resin to form an impregnated yarn or cord.
  • the size composition include various processing aids which aid in improving the bonding relationship between the thermoplastic resin and the glass fibers.
  • these processing aids remain in the impregnated strand.
  • the processing aids are undesirable materials when clean thermoplastic impregnated glass fibers are desired, such as for use in producing high performance thermoplastic impregnated fibrous strand.
  • thermoplastic resin when directly blended with the thermoplastic resin during the glass fiber forming process, produces a substantially pure thermoplastic impregnated glass strand.
  • a slurry composition for impregnating glass fibers which includes a thermoplastic resin and fugitive processing aids such as a binder or film former material and a thickening agent (or rheology modifier).
  • the slurry composition of the present invention includes the use of fugitive processing components together with a non-fugitive polymer to obtain a "prepreg" of the non-fugitive polymer.
  • the slurry composition is applied to the glass fiber during the fiber forming operation.
  • the composition of this invention can thus be applied as a size for glass fibers during the fiber forming operation and the resulting sized thermoplastic impregnated glass fibers can then be fabricated into glass fiber reinforced products.
  • the slurry composition of the present invention provides a sized glass fiber impregnated with a compatible polymeric
  • the impregnated glass fiber is free of undesired processing materials and is therefore useful for various high performance glass reinforced end use items.
  • Figure 1 is a graph showing the thermogravimetric analysis of a slurry containing polyphenylene sulfide.
  • Figure 2 is a graph showing the thermogravimetric analysis of a glass fiber impregnated with the slurry shown in Figure 1.
  • the present invention relates to a slurry composition useful for producing an improved yarn or strand (bundle of filaments) pre- impregnated with a thermoplastic polymer during the filament forming operation.
  • glass fibers as used herein shall mean filaments formed by attenuation of one or more streams of molten glass and to strands formed when such glass fiber filaments are gathered together in the forming process.
  • the term shall also mean yarns and cords formed by applying and/or twisting a multiplicity of strands together and to woven and non-woven fabrics which are formed of such glass fiber strands, yarns, or cords.
  • the composition of this invention may contain a carrier solvent, normally water, a coupling agent, and fugitive processing aids such as a binder or film former material, a thickener or rheology modifier material, and a matrix thermoplastic resin
  • any suitable coupling agent can be employed in the successful practice of this invention.
  • the coupling agent acts to produce adhesion between the matrix resin and provide strength development and retention of the matrix resin in the slurry.
  • a - _ suitable coupling agent is a silane such as a diamine silane (Z6020 from Dow Corning).
  • the coupling agent can be contained in an amount of about 1.2 percent, by weight, of the slurry mixture.
  • any suitable fugitive binder material can be employed.
  • the fugitive thickener material may be the same Q materials as the binder material.
  • the binder or film former material aids in the handling and processing of the filament during the fiber forming process.
  • Suitable binder or film former materials are, for example, epoxy, polyester, polyvinyl acetate, polyv ⁇ nyl alcohol, acrylics, or other chemicals which have the ability to bond the 5 thermoplastic powder particles to the fiber upon the evaporation of the water or which have the ability themselves to suspend the particles in the slurry and subsequently bond themselves to the fiber.
  • a suitable fugitive binder material is polyethylene oxide.
  • the binder material will be contained in an amount within the range of from about 1.0 to about 1.2 percent, by weight, of the slurry mixture.
  • any suitable fugitive thickener material can be employed.
  • the thickener material acts as a rheology modifier so that the thermoplastic powder particles will actually adhere to the fiber. Without the thickener material the thermoplastic powder particles may stay behind on the rolls of the applicator while the carrier solvent goes on the fiber. The result would be a rapid build-up of powder on the applicator rolls, which in turn, rapidly causes fiber breakage.
  • thermoplastic resins are dispersed into the sizing in the form of fine particles.
  • a resin is polyphenylene sulfide.
  • the size of the powder particles are less than about 125 microns.
  • the resin powders can be applied to the filaments in an amount within the range of of between about 5 to about 50 percent, by weight, of the final prepreg yarn or strand.
  • the sizing composition According to the present invention the sizing composition
  • thermoplastic powder particles 25 suspends the thermoplastic powder particles in the slurry.
  • the slurry compositions of this invention are best produced by blending all materials in their liquid state with agitation. A uniform coating of the composition can be applied to the glass fibers in any suitable
  • compositions of the present invention are applied to the surface of the glass fiber in the manner described in the co-pending U.S. Application Serial No. 07/269,089, filed November 9, 1988 now U.S. Patent No. , issued , which is a
  • the resultant slurry composition is sufficiently liquid to be applied to the fibers during the fiber-forming operation.
  • Each fiber is coated by the slurry mixture as the fibers are formed, that is, at or about the place in their formation where the conventional size compositions are typically applied (e.g., between the bushing and the spindle on which the fibers are wound as a package).
  • the continuous fibers leave the bushing and are dipped into the slurry and are impregnated with the slurry.
  • organic or inorganic particulates such as metallic fillers useful in producing conductive rovings, may also be used with the thermoplastic polymer powder particles. These fillers can either be pre-combined with the polymer so that each powder particle contains polymer and filler or be added separately as a powder to the slurry.
  • the resultant impregnated strands can be chopped, either before or after drying, to be used for such operations as injection molding.
  • Continuous thermoplastic impregnated strands can be filament wound or pultruded to achieve thermoplastic fiber reinforced end use items.
  • High performance thermoplastic resins exhibit advantages over thermosetting polymers when used as a matrix resin in fiber reinforced compositions. These advantages include better high temperature performance, better hydrolysis resistance, better impact properties, better electrical properties, better chemical resistance _ n and better dielectric properties.
  • thermoplastic strands A convenient way to fabricate a fiber reinforced high performance thermoplastic is to use pre-impregnated thermoplastic strands. This is especially useful for high performance thermoplastic reinforced with continuous fibers.
  • This invention describes such a 5 thermoplastic pre-impregnated strand.
  • a thermoplastic powder is dispersed in water. Usually, a surfactant is added to the water to help wetting of the powder.
  • a thickener usually a water soluble polymer, is added to build-up the viscosity of the liquid phase.
  • Other additives such as silane coupling agents can also be added to the aqueous suspension (also called
  • slurry This slurry is used as a size and applied to glass fibers as they are being formed, as disclosed in the co-pending patent application Serial No. 07/269,089, discussed above.
  • the thickener is chosen so that it is thermally decomposed into volatile products at a temperature inferior to the decomposition temperature of the thermoplastic powder and which is decomposed in the presence of this thermoplastic, even after this thermoplastic has been fused, without objectionally deteriorating the properties of this thermoplastic.
  • thickeners include polyethylene oxide, hydroxypropyleellulose, starch, and hydroxyethylcellulose. This thickener may also be used as a "binder".
  • the binder is used to hold the thermoplastic powder on the strand of fibers upon drying, and therefore providing an impregnated strand having good integrity.
  • the binder may be an additional ingredient added to the slurry; however, the thickener chosen is also thermally decomposable.
  • the wetting agents chosen are also volatile or thermally decomposable at an appropriate temperature.
  • thermoplastic impregnated fiber is heated to a temperature above the fusing temperature of the thermoplastic powder so that the powder is totally or partially fused or held to the fibers without having to rely on a binder.
  • This heating step may include, or be preeeeded by, partial decomposition of the fugitive ingredients, thus, completing decomposition of the fugitive ingredients at a temperature above or below the fusing temperature of the thermoplastic. Any of these steps may be combined with modification of the thermoplastic such as "curing" or "annealing".
  • a slurry of the following composition is prepared: 1200 parts Ryton VI through 115 mesh (equivalent dry powder); 2764 parts water/surf; add 48 parts polyethylene oxide (Polyox WSR 205 from Union Carbide) mix well until homogeneous. This provides a slurry 5 containing 31.1% solids.
  • the glass fibers are coated as they are being formed with the slurry described above.
  • the slurry is applied with a standard size applicator fitted with a doctor blade to control the film thickness on the applicator roll.
  • the package #1 is dried for one day at room conditions.
  • the package (after substituting a steel for a cardboard forming tube) is 5 then placed in an air oven at 300°C for 1 hour.
  • the polyphenylene sulfide fuses, the polyoxyethylene oxide thermally decomposes into volatile matter and the polyphenylene oxide cures into a higher molecular weight polymer.
  • the strand of impregnated glass can be easily unwound from the package inspite of the high amount of impregnating resin.
  • This strand is filament wound in a mold to form a unidirectional composite.
  • the strands can then be compression molded into end use items.
  • the measured flexural strength of 8014.2 kg/sq.cm. (114 k psi) indicates that the strand has useful mechanical properties.
  • Package #2 is dried in the same manner as package #1 but before fusing the polyphenylene sulfide the strand is wound onto a plate to form unidirectional layers.
  • the plate is then placed in an oven at 300°C for 1 hour as was done for package #1 above.
  • the unidirectional layers fuse into a sheet which can later be used for compression molding unidirectional composites.
  • the measured flexural strength is 8436 kg/sq.cm. (120,000 psi) which also indicates useful mechanical properties.
  • a fine powder (__.125 microns) of a high performance thermoplastic such as polyphenylene sulfide powder (Ryton VI from Phillipps Chem.) is dispersed in a water solution of a wetting agent in the following proportions: (parts by weight) 1200 parts water; 4 parts Tergitol Nin Foam 2 x (from Union Carbide) add: 800 parts Ryton VI and stir until good wetting is achieved; add 14800 parts water and stir.
  • This slurry is poured in small quantities through a 115 mesh sieve to separate the powder into coarse and fine fractions. The slurry is passed through the sieve, collected and allowed to settle for at least 12 hours. The powder which has settled is collected by passing through 115 mesh.
  • the slurry of the following composition is prepared: 1200 parts Ryton VI through 115 mesh (equivalent dry powder); 2764 parts water/surf; add 42 parts polyethylene oxide (Polyox WSR 205 from Union Carbide) and 48 parts diamine silane (Z6020 from Dow Corning). This provides a slurry containing 31.8% solids.
  • the glass fibers are coated as they are being formed with the slurry described above.
  • the slurry is applied with a standard size applicator fitted with a doctor blade to control the film thickness on the applicator roll. A forming package having 2000 filaments/strands is made.
  • the package is dried for one day at room conditions.
  • the strand is wound onto a plate to form unidirectional layers.
  • the plate is then placed in an air oven at 300° C for 1 hour.
  • the polyphenylene sulfide fuses, the polyoxyethylene oxide thermally decomposes into volatile matter and the polyphenylene sulfide cures into a higher molecular weight polymer.
  • the unidirectional layers fuse into a sheet which can be used for compression molding unidirectional composites.
  • the measured flexural strength indicates useful mechanical properties: 10545 to 13357 kg/sq.cm. (150,000 to 190,000 psi) depending on molding conditions which indicates useful mechanical properties.
  • Thermogravimetric analysis confirms the removal of fugitive components through thermal degradation.
  • TGA Thermogravimetric analysis
  • Figure 1 shows that pure polyphenylene sulfide (PPS) exhibits nearly no degradation below 300°C and very little loss weight up to 500°C.
  • PPS polyphenylene sulfide
  • polyethylene oxide used as a fugitive thickener and binder starts to degrade at 200°C and has nearly completely volatilized by the time the temperature reaches 400° C.
  • the solid curve shows the weight loss of the dried slurry as the temperature increases.
  • the weight loss from 200°C up to point A is due to the loss of polyethylene oxide in the slurry.
  • the loss in weight in the remaining PPS in the dried slurry is essentially the same as the loss in weight in pure PPS.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Materials Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Reinforced Plastic Materials (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Surface Treatment Of Glass Fibres Or Filaments (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

Composition aqueuse d'encollage pour fibres de verre. Elle comprend une poudre de résine polymère thermoplastique, un agent d'accrochage, et des auxiliaires volatils de transformation tels que des liants ou des filmogènes. On applique la composition aux surfaces des fibres de verre pendant le processus de formation de fibres. On peut ajouter à la composition d'encollage un matériau volatil modifiant la rhéologie. Dans un mode de réalisation, on a prévu un matériau liant en oxyde de polyéthylène ainsi qu'une résine polymère thermoplastique de sulfure de polyphénylène.
EP91908021A 1991-04-16 1991-04-16 Composition d'encollage pour l'impregnation de filaments orientes Withdrawn EP0534981A1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US1991/002499 WO1992018431A1 (fr) 1991-04-16 1991-04-16 Composition d'encollage pour l'impregnation de filaments orientes

Publications (1)

Publication Number Publication Date
EP0534981A1 true EP0534981A1 (fr) 1993-04-07

Family

ID=22225451

Family Applications (1)

Application Number Title Priority Date Filing Date
EP91908021A Withdrawn EP0534981A1 (fr) 1991-04-16 1991-04-16 Composition d'encollage pour l'impregnation de filaments orientes

Country Status (5)

Country Link
EP (1) EP0534981A1 (fr)
JP (1) JPH05507676A (fr)
KR (1) KR930701355A (fr)
BR (1) BR9106691A (fr)
WO (1) WO1992018431A1 (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2725979B1 (fr) * 1994-10-21 1996-11-29 Vetrotex France Sa Fils de verre ensimes destines au renforcement de matieres organiques
WO2003082565A1 (fr) * 2002-04-03 2003-10-09 Tenax Fibers Gmbh Materiau composite, procede de fabrication et utilisation dudit materiau composite
JP7368929B2 (ja) * 2017-08-08 2023-10-25 株式会社日本製鋼所 繊維強化樹指中間材の製造方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2778764A (en) * 1951-09-13 1957-01-22 Owens Corning Fiberglass Corp Method of sizing glass fibers to form strands
US3498826A (en) * 1966-03-30 1970-03-03 Owens Corning Fiberglass Corp Treated glass fibers and fabrics formed thereof
GB1264432A (fr) * 1969-04-28 1972-02-23
SE8100819L (sv) * 1981-02-05 1982-08-06 Kema Nord Ab Hartsimpregnerat fiberkompositmaterial

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9218431A1 *

Also Published As

Publication number Publication date
KR930701355A (ko) 1993-06-11
BR9106691A (pt) 1993-06-29
WO1992018431A1 (fr) 1992-10-29
JPH05507676A (ja) 1993-11-04

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