EP0426698A1 - Fibre-containing reinforcing material and a method of making said material - Google Patents

Fibre-containing reinforcing material and a method of making said material

Info

Publication number
EP0426698A1
EP0426698A1 EP89907351A EP89907351A EP0426698A1 EP 0426698 A1 EP0426698 A1 EP 0426698A1 EP 89907351 A EP89907351 A EP 89907351A EP 89907351 A EP89907351 A EP 89907351A EP 0426698 A1 EP0426698 A1 EP 0426698A1
Authority
EP
European Patent Office
Prior art keywords
fibre
fibres
carbon
weight
reinforcing material
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Withdrawn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
EP89907351A
Other languages
German (de)
English (en)
French (fr)
Inventor
Ingegerd Hjorth
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.)
Honeywell Safety Products Sweden AB
Original Assignee
Bilsom AB
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 Bilsom AB filed Critical Bilsom AB
Publication of EP0426698A1 publication Critical patent/EP0426698A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • C08K3/36Silica
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K7/00Use of ingredients characterised by shape
    • C08K7/02Fibres or whiskers
    • C08K7/04Fibres or whiskers inorganic
    • C08K7/06Elements
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K7/00Use of ingredients characterised by shape
    • C08K7/02Fibres or whiskers
    • C08K7/04Fibres or whiskers inorganic
    • C08K7/14Glass

Definitions

  • the present invention relates to a fibre-containing reinforcing material and to a method of making such a material.
  • Fibre-reinforcing of materials having low tensile strength and low resistance is previously known.
  • different materials have been reinforced with fibres of different types, such as glass, steel, mineral wool and plastic fibres.
  • Fibre-reinforcement mainly aims at increasing the toughness of the material , which, in conjunction with a higher tensile strength, also affects other characteristics and improves the impact strength, wear resistance and dimensional stability of the material.
  • Fibre-reinforced materials are used in many types of products, from sports articles to jet aircraft com ⁇ ponents.
  • technology is still requiring new composite materials having high strength, resistance to fracture and oxidation stability at elevated tempera ⁇ tures.
  • the present invention aims at obviating or reducing the difficulties ensuing from insufficient strength, resistance to fracture and oxidation stability in con ⁇ nection with prior art composite materials.
  • This object is achieved in that the invention provides a fibre-con- taining reinforcing material which, when used in the production of fibre-reinforced composite materials, imparts to these materials high strength values also at elevated temperatures of about 100-120°C.
  • the length and diameter of the fibres and their chemical and physical surface structure are, inter alia, the length and diameter of the fibres and their chemical and physical surface structure.
  • the length/ diameter ratio should be as high as possible.
  • the L/D number i.e. the fineness of the filament
  • Glass filaments of the type roving normally have a diameter of between 10 and 20 ⁇ m, while the filament length may vary between a few millimetres up to several centimetres.
  • the limitations of roving type filaments lie in the diameter which cannot be reduced below about 8-10 ⁇ m.
  • the present invention aims at providing a solution to the problem of defibrating carbon fibre bundles into individiual carbon fibres and, furthermore, at providing a homogeneous mixture consisting of carbon fibres and glass fibres and serviceable as a reinforcing material in the production of composite materials.
  • the present invention provides a fibre- containing reinforcing material which is characterised in that it comprises an essentially homogeneous distribu ⁇ tion of carbon fibres, glass fibres, hydrophobic, anionic, colloidal silica and cationic talc, the weight ratio of carbon fibres to glass fibres being from 1:99 to 99:1, the silica forming about 5-20% by weight of the total fibre weight, and the talc forming about 5-20% by weight of the total fibre weight.
  • the invention also provides a method of making a fibre-containing reinforcing material, a method which is characterised by a) adding, to carbon fibre bundles, hydrophobic, anionic, colloidal silica in an amount of about 5-20% by weight, based on the total fibre weight of the final reinforcing material, the carbon fibre bundles being divided into individual fibres by mixing under shear action in dry con ⁇ dition; b) adding, to said mixture of carbon fibres and silica, glass fibres in an amount to give a weight ratio of carbon fibres to glass fibres of from 1:99 to 99:1; and c) distributing, in said mixture of carbon fibres, silica and glass fibres, about 5-20% by weight, based on the total fibre weight, of cationic talc.
  • the invention also comprises the use of the above-mentioned fibre-containing reinforcing material for the production of fibre-reinforced composite mate ⁇ rials.
  • the fibre-containing reinforcing material according to the invention contains four principal components, i.e. carbon fibres, glass fibres, hydrophobic, anionic, colloidal silica, and cationic talc. These components and the restrictions placed thereon in the context of the invention will be explained below.
  • the carbon fibres used in the context of the in ⁇ vention are of conventional type and are initially in the form of carbon fibre bundles. This raw material and the production thereof are well known and need not be described in detail.
  • the dimensions of both the carbon fibre bundles and the individual carbon fibres may vary within wide limits. Generally, however, the carbon fibre bundles have a mean diameter of about 10-15 ⁇ m, and each bundle comprises about 10-20 individual fibres.
  • the carbon fibre bundles are produced in relatively large lengths that are cut into smaller lengths of about 1 cm or less.
  • carbon fibre bundles (and thus carbon fibres) having a mean length of about 0.5-6.0 mm are preferred.
  • the reinforcing effect of the carbon fibre deteriorates at values below about 0.5 mm, while it is difficult to homogeneously admix and distribute carbon fibres longer than about 6.0 mm in the matrix of a composite material.
  • the L/D ratio of the fibre i.e. the fineness number, should be selected such that optimal characteristics are obtained in respect of reinforcing effect and homogeneous distribution within the matrix.
  • the reinforcing material according to the invention also comprises glass fibres. Also glass fibres and their production method are so well known that no detailed description is necessary.
  • the invention uses glass fibres which from the very beginning are in the form of individual fibres, in con ⁇ trast to, for example, roving where the filaments are firmly bound together and therefore not readily separable.
  • the glass fibres used in the context of the invention should be relatively thin and preferably have a mean diameter of about 0.5-6.0 ⁇ m, most preferred about 0.8-3.0 ⁇ m. Furthermore, a mean fibre length of about 0.5-15 mm is preferred, about 0.8-3 mm being most preferred. Within these diameter and length ranges, the desired high fineness numbers are obtainable which permit optimal mutual adjustment of a good reinforcing effect and sim ⁇ plicity of admixture to and distribution in the matrix material.
  • the invention is not restricted to the use of glass fibres of any special type or glass composition and, in principle, all types of glass fibres suitable as reinforcing fibres may be used.
  • An especially preferred glass fibre type are glass fibres of so-called C glass.
  • both the amount of carbon fibres and the amount of glass fibres in the fibre-containing reinforcing material according to the invention may be varied within wide limits.
  • the weight ratio of carbon fibres to glass fibres may vary from about 1:99 to about 99:1, preferably from about 10:90 to about 40:60. It is prefer ⁇ red to use a lower proportion of carbon fibres which are more expensive than glass fibres.
  • the third component of the fibre-containing re ⁇ inforcing material according to the invention is hydro- phobic, anionic, colloidal silica.
  • the principal object of the silica in the context of the invention is to serve as a dispersing agent for dividing the carbon fibre bundles into indiviual fibres. Without being bound to any specific theory, it is assumed that the silica penetrates into the fibre bundles and is distributed on the surface of the individiual carbon fibres, thus imparting to the fibres a negative charge which has a repelling effect conducive to fibre separation.
  • Colloidal silica is obtainable in several different forms, among them
  • silica aerogel which is a colloidal silica which is produced by replacing the water of a silica hydrogel by a low-boiling water-miscible liquid, heating in an autoclave above the critical tempe ⁇ rature of the liquid, and then venting the auto ⁇ clave;
  • fumed or pyrogenic silica which is a colloidal silica obtained by burning silicon tetrachloride and collecting the resulting silica fumes;
  • colloidal silica is generally in the form of agglom ⁇ erates built up of extremely small primary particles of a size within the range of about 5-20 nm. The extremely small size of the primary particles imparts to colloidal
  • silica a large surface area of about 50-400 m /g or more.
  • Colloidal silica usually is hydrophilic, but the inventor has found that it should be hydrophobic for a successful division and separation of the carbon fibre bundles. To the extent that the silica is not initially hydrophobic, it can be made hydrophobic by a special surface treatment which, per se, is previously known.
  • the invention prefers colloidal silica of the so-called fumed type, and an especially preferred silica is the one marketed by Degussa under the tradename Aerosil R 972.
  • silica Among other types of silica, mention may be made of the one which is marketed by Cabot Corporation under the trade name Cab-0-Sil.
  • the amount of silica is about 5-20% by weight, preferably about 5-15% by weight, based on the total fibre weight. Generally, it may be said that the amount of silica should be suffi- cient to coat also the surface of the glass fibres, thereby to provide a more uniform charge distribution in the fibres.
  • the fourth component of the fibre-containing re ⁇ inforcing material according to the invention is cationic talc, preferably the variant known as soapstone. Soapstone is greenish-grey, while talc is practically white.
  • talc usually includes (a) the mineral talc, (b) steatite which is a compact variant of talc, and (c) the rock type soapstone.
  • the mineral talc is a hydrated magnesium silicate of the ideal composition Mg ⁇ i.O. Q (OH) lake .
  • the talc content of commercial talc is high and usually lies at about 97% by weight.
  • talc mineral is crushed and comminuted and then purified by flotation to give a talc product having a high talc content and whiteness.
  • Soapstone is a natural product consisting minera- logically of talc mixed with a high content of chlorite and minor amounts of carbonate and amphibole.
  • soapstone from Hand ⁇ l in Sweden has the following mineral composition talc about 67% by weight chlorite about 18% by weight carbonate about 8% by weight amphibole about 3% by weight ore material about 4% by weight
  • mineral talc is the one obtainable under the trade name Finntalk P40 from Outokumpu Oy, Finland. It has a mean diameter of about 10-20 ⁇ m, a talc content of about 97% by weight, a loss on ignition of 7% by weight, and an oil absorption value of 32 g oil/100 g talc.
  • the melting point is 1375°C.
  • soapstone type H340 As an example of a soapstone suitable in the context of this invention, mention may be made of the soapstone type H340 from Hand ⁇ l, Sweden. This is a micronised soapstone having a mean diameter of 5-10 ⁇ m. The talc content is about 67% by weight, and the loss on ignition about 8% by weight. The oil absorption value is 55 g oil/100 g soapstone, and the melting point is 1500°C.
  • talc minerals and soapstone may vary within wide limits, preferably from a weight ratio of about 30:70 to about 70:30, more preferred from about 40:60 to about 60:40, and most preferred about 50:50.
  • the particle size of the talc is not critical in the invention, but usually lies within the range of about 5-10 ⁇ m.
  • the talc is cationic, and by incorporating talc in the fibre-containing reinforcing material of the invention it is intended to make the talc act as a cationic additive to the anionic carbon fibres and the glass fibres, but also to the matrix material which is preferably selected among anionic polymer materials, such as polyolefins (polyethylene, polypropylene), polyvinyl chloride, polyesters, poly- acrylates and polymethacrylates, polyurethanes, bituminous products, etc.
  • the amount of talc in the fibre-containing rein ⁇ forcing material according to the invention may vary within wide limits and is generally about 5-20% by weight, based on the total fibre weight.
  • carbon fibre bundles are slushed to divide the bundles into individual carbon fibres which are then separated from one another.
  • the slushing and separating step is carried out by mixing the carbon fibre bundles under shear action in the dry state.
  • this treatment will be called dry dispersion hereinafter. It was found that, for dry dispersion, it is not enough that the carbon fibre bundles are mixed under the action of shear forces in order to obtain a satisfactory carbon fibre separation.
  • the dry dispersion of the carbon fibre bundles can be carried out in any machine mixing the carbon fibre bundles under the action of shear forces.
  • Suitable machines for dry dispersion in accordance with the invention are high-speed mixers of the type L ⁇ dige, Drais or Cowles-Dissolver. The mixer is adjusted to a suitable operating speed, preferably 1000-3000 rp , and dry dispersion is carried out for a time sufficient to achieve satisfactory separation, which is easily seen from a routine check for which the dry-dispersed fibre mixture is combined with matrix material and spread on a glass plate. If the spread-out fibres show an isotropic distribution in the matrix, the dry dispersion is satisfactory.
  • the dry dispersion time usually is about 10-30 min.
  • glass fibres are supplied to the carbon fibre mixture.
  • the parameters of the glass fibres are those mentioned above, and the glass fibres are added to the dry dispersion machine.
  • the glass fibres may be supplied after the dry dispersion of the carbon fibre bundles has been terminated, they are usually added at the final stage of the dry dispersion of the carbon fibre bundles (for example after about 10-12 min. of dry dispersion). In both cases, operation of the mixer is continued to achieve an essentially homogeneous distri bution of the glass fibres among the carbon fibres.
  • the glass fibres are from the beginning in the form of individual, extremely thin fibres having a negative surface charge.
  • the surfac charge level may vary between the carbon fibres and the glass fibres
  • the glass fibres are added to the system of carbon fibres and colloidal silica, the glass fibres are highly uniformly distributed during the continued dispersion and mixed to form an entirely homogeneous system with the carbon fibres and the silica.
  • the mixing time after the glass fibres have been added preferably amounts to about 5-15 min.
  • cationic talc preferably soapstone as defined above
  • talc acts as an adhesion agent between the fibres and the matrix of the composite material.
  • talc is a material having a cationic, hydrophobic surface, and by its positive surface charge the talc gives an excellent adhesion to the negatively charged fibres and, simultaneously, good adhesion to the matrix material which preferably is anionic, such as anionic polymer materials of the type mentioned above.
  • the carbon fibres primarily give an improved impact strength to the composite material, while the other constituents also provide substantially higher rigidity and dimensional stability at higher temperatures.
  • the talc is added by dry dispersion, and this applies also to the remaining constituents, the dry dispersion being conducted until the talc has been substantially homogeneously distributed in the mixture, which is usually achieved within about 5 min.
  • novel fibre-containing reinforcing material according to the invention which is hydrophobic in character and in which a chemical and physical inter ⁇ action occurs between carbon fibres and glass fibres, and also with the matrix material, excellent adhesion between the components of the composite material is obtained, and it has surprisingly been found that the strength values and the stability of the composite ma ⁇ terial can largely be maintained at more than 90% also at elevated temperatures, for example a temperature of 120°C for 200 hours.
  • the corresponding values after a similar heat treatment of rovings and glass fibres alone or carbon fibres alone are about 60-70%.
  • the fibres should be isotropically oriented, i.e. uni- formly distributed in all directions. In conventional technique, however, the fibres are oriented more or less perpendicular to the direction of flow during form ⁇ ing, which results in an anisotropic distribution and strength.
  • the fibre-containing reinforcing material according to the invention has surprisingly been found to give an isotropic fibre orientation, which means a uniformly distributed strength of the material. It is assumed that this isotropy is the result of the charges of the components included and the interaction established between carbon fibres and glass fibres and also between carbon fibres, glass fibres and matrix material.
  • Material for the production of the fibre-containing reinforcing material according to the invention in the percentages indicated in the Table below, were batched into a high-speed L ⁇ dige type mixer of high shear action, which was operated at about 2000 rpm.
  • the carbon fibre bundles had a length of about 3 mm and a diameter of about 10-15 ⁇ m.
  • Each bundle contained about 10-20 in- dividual carbon fibres having a diameter of about 0.7 ⁇ m.
  • the L/D number of the carbon fibres was 4280.
  • the glass fibres consisted of C glass and had a mean length of about 2.7 mm and a mean diameter of about 0.8 ⁇ m.
  • the L/D number of the glass fibres was about 3375.
  • the hydro- phobic, anionic, colloidal silica was Aerosil ® R 972 from Degussa.
  • the talc was soapstone H-340 from Hand ⁇ l.
  • Crastine S 600 which is a polyester plastic from Ciba-Geigy.
  • the amount of admixed reinforcing material was 20% by weight.
  • the carbon fibre bundles were first dry-dispersed for about 10 min. together with the silica, whereupon the glass fibres were added, and dry dispersion was continued for about 15 min. Then the soapstone was added, and dry dispersion was continued for about 5 min. more.
  • the reinforcing material according to the invention can be used for a variety of applications and a variety of products, such as reinforcing material in safety helmets, straps for ear muffs, car components and many other articles for which a preferably isotropic fibre reinforcement is required.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Reinforced Plastic Materials (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
EP89907351A 1988-07-20 1989-06-16 Fibre-containing reinforcing material and a method of making said material Withdrawn EP0426698A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE8802681A SE461593B (sv) 1988-07-20 1988-07-20 Fiberinnehaallande armeringsmaterial, foerfarande foer framstaellning daerav samt anvaendning av armeringsmaterialet i ett kompositmaterial
SE8802681 1988-07-20

Publications (1)

Publication Number Publication Date
EP0426698A1 true EP0426698A1 (en) 1991-05-15

Family

ID=20372943

Family Applications (1)

Application Number Title Priority Date Filing Date
EP89907351A Withdrawn EP0426698A1 (en) 1988-07-20 1989-06-16 Fibre-containing reinforcing material and a method of making said material

Country Status (5)

Country Link
EP (1) EP0426698A1 (da)
DK (1) DK8691A (da)
FI (1) FI910287A7 (da)
SE (1) SE461593B (da)
WO (1) WO1990001045A1 (da)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI950716L (fi) * 1995-02-17 1996-08-18 Borealis As Palosuojattu polymeerikoostumus
US11365306B2 (en) * 2017-11-29 2022-06-21 Pirelli Tyre S.P.A. Microbeads comprising silicate fibres with needle-shaped morphology of nanometric size, preparation thereof, elastomeric compositions and tyres for vehicles comprising them

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1576501A (en) * 1976-02-09 1980-10-08 Carborundum Co Refractory mouldable composition
DE3148326C2 (de) * 1981-12-07 1984-09-13 Keramchemie GmbH, 5433 Siershahn Teigige Formmasse
US4735659A (en) * 1986-08-18 1988-04-05 Phillips Petroleum Company Compositions and a process for preparing water dispersible polymers

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9001045A1 *

Also Published As

Publication number Publication date
DK8691A (da) 1991-01-21
SE8802681D0 (sv) 1988-07-20
FI910287A0 (fi) 1991-01-18
SE461593B (sv) 1990-03-05
DK8691D0 (da) 1991-01-18
SE8802681L (sv) 1990-01-21
FI910287A7 (fi) 1991-01-18
WO1990001045A1 (en) 1990-02-08

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