WO2021049369A1 - ガラスフィラー及び樹脂組成物 - Google Patents

ガラスフィラー及び樹脂組成物 Download PDF

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Publication number
WO2021049369A1
WO2021049369A1 PCT/JP2020/033033 JP2020033033W WO2021049369A1 WO 2021049369 A1 WO2021049369 A1 WO 2021049369A1 JP 2020033033 W JP2020033033 W JP 2020033033W WO 2021049369 A1 WO2021049369 A1 WO 2021049369A1
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Prior art keywords
glass
resin
mass
composition
sio
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Ceased
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PCT/JP2020/033033
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English (en)
French (fr)
Japanese (ja)
Inventor
加藤　伸一
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Nippon Sheet Glass Co Ltd
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Nippon Sheet Glass Co Ltd
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Application filed by Nippon Sheet Glass Co Ltd filed Critical Nippon Sheet Glass Co Ltd
Priority to CN202080062587.2A priority Critical patent/CN114364730A/zh
Priority to EP20863173.9A priority patent/EP4029842A1/en
Priority to JP2021545236A priority patent/JP7377275B2/ja
Priority to US17/641,731 priority patent/US20220298376A1/en
Publication of WO2021049369A1 publication Critical patent/WO2021049369A1/ja
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04—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
    • 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
    • C03C25/32—Macromolecular compounds or prepolymers obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
    • C03C25/36—Epoxy 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
    • C03C25/24—Coatings containing organic materials
    • C03C25/40—Organo-silicon compounds
    • 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
    • C03C25/465—Coatings containing composite materials
    • 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
    • C03C3/00—Glass compositions
    • C03C3/04—Glass compositions containing silica
    • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
    • C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
    • C03C3/091—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00—Use of pretreated ingredients
    • C08K9/04—Ingredients treated with organic substances
    • C08K9/06—Ingredients treated with organic substances with silicon-containing compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black

Definitions

  • the present invention relates to a glass filler and a resin composition containing the same.
  • glass fibers For resin molded products, glass fibers, carbon fibers, mica, glass beads, flake-shaped glass, etc. are used for the purpose of reducing warpage and deformation (that is, improving dimensional stability) and / or improving mechanical strength. It is generally known to be blended with a matrix resin as a filler.
  • Glass fiber is widely used as a resin reinforcing filler that can impart higher mechanical strength to resin molded products than flake-shaped and spherical glass fillers.
  • a resin molded product containing glass fibers there may be a problem of dimensional stability such as a tendency for warpage to occur. Therefore, in order to improve dimensional stability without significantly reducing the mechanical strength of the resin molded product, a pulverized product (glass milled fiber) obtained by crushing glass fiber may be used as a filler for reinforcing the resin. is there.
  • Patent Documents 1 and 2 in order to further improve the dimensional stability of the resin molded product, among the glass milled fibers, glass fibers having a flat shape instead of a circular cross section were pulverized. It has been proposed to use glass milled fiber as a filler.
  • the glass milled fiber having a flat cross-sectional shape can improve both the mechanical strength and the dimensional stability of the molded product of the resin when it is blended with the resin as a filler.
  • the glass milled fiber having a flat cross-sectional shape has a fiber shape, when the fiber length is relatively long, the resin molded product may not be able to obtain sufficiently high dimensional stability.
  • the fiber length of the glass milled fiber having a flat cross-sectional shape is shortened for the purpose of improving the dimensional stability, the dimensional stability is improved, but the mechanical strength may be lowered.
  • a glass milled fiber having a flat cross-sectional shape is used as a filler for reinforcing a resin, it has been difficult to realize both high mechanical strength and excellent dimensional stability of the resin molded product.
  • one of the objects of the present invention is to provide a glass filler capable of imparting both high mechanical strength and excellent dimensional stability to a molded product of the resin when blended with the resin. is there.
  • Yet another object of the present invention is to provide a resin composition in which such a glass filler is blended with a resin to realize a resin molded product having both high mechanical strength and excellent dimensional stability. It is to be.
  • the present invention With a glass substrate A coating film containing a surface treatment agent that covers at least a part of the surface of the glass substrate, and Is a glass filler containing
  • the glass base material is a glass fiber having a flat cross-sectional shape.
  • the length corresponding to the minor axis in the flat cross section of the glass fiber is represented by L1 and the length corresponding to the major axis is represented by L2, and the length corresponding to the fiber length of the glass fiber is referred to as L3.
  • the ratio of the mean value of L2 to the mean value of L1 (mean value of L2) / (mean value of L1) is 1.5 or more and 8 or less, and the mean value of L1 is 1.0 ⁇ m or more and 10 ⁇ m or less. Yes, and the average value of L3 is 80 ⁇ m or more and 160 ⁇ m or less.
  • the surface treatment agent contains a silane coupling agent and contains.
  • the content ratio of the coating film in the glass filler is 0.05% by mass or more and 2.5% by mass or less. Provide a glass filler.
  • the present invention also provides a resin composition containing the above-mentioned glass filler of the present invention and a matrix resin.
  • the glass filler of the present invention When blended with a resin, the glass filler of the present invention can impart both high mechanical strength and excellent dimensional stability to a molded product of the resin. Further, since the resin composition of the present invention contains such a glass filler of the present invention, it is possible to realize a resin molded product having both high mechanical strength and excellent dimensional stability.
  • the perspective view which shows the example of the glass base material in the glass filler of embodiment of this invention The perspective view which shows another example of the glass base material in the glass filler of embodiment of this invention.
  • the glass filler of the present embodiment includes a glass base material and a coating film containing a surface treatment agent that covers at least a part of the surface of the glass base material.
  • the glass substrate is a glass fiber having a flat cross-sectional shape.
  • L1 length corresponding to the minor axis in the flat cross section of the glass fiber
  • L2 length corresponding to the major axis
  • L3 length corresponding to the fiber length of the glass fiber
  • the average value of L3 is 80 ⁇ m or more and 160 ⁇ m or less.
  • the surface treatment agent contained in the coating film contains a silane coupling agent.
  • the content ratio of the coating film in the glass filler of the present embodiment is 0.05% by mass or more and 2.5% by mass or less.
  • the cross section of the glass fiber is a cross section in the direction perpendicular to the fiber axis of the glass fiber, and the fiber length of the glass fiber is parallel to the fiber axis of the glass fiber.
  • the minor axis in the flat cross section refers to the longest length in the thickness direction of the flat cross section, that is, the longest length in the direction parallel to the shortest portion in the cross section.
  • the major axis in a flat cross section refers to the longest length in the direction perpendicular to the minor axis.
  • the flat cross-sectional shape means that the cross section has a flat shape as a whole.
  • FIG. 1A to 1C are perspective views showing an example of a glass base material in the glass filler of the present embodiment.
  • Examples of the flat cross-sectional shape include a cocoon type (see FIG. 1A), a ribbon type (see FIG. 1B), and a dumbbell type (see FIG. 1C).
  • the average value of the length L3 corresponding to the fiber length of the glass fiber is the length L3 corresponding to the fiber length of 500 arbitrarily selected glass base materials, and the optical microscope of the glass base material. It is the number average length obtained from the measurement results obtained by measuring using an image. Further, the average value of the length L1 corresponding to the minor axis and the average value of the length L2 corresponding to the major axis in the flat cross section of the glass fiber are the scanning electrons of the cross section of 100 arbitrarily selected glass substrates. It is a value obtained by measuring the lengths of the minor axis and the major axis defined above using a scanning electron microscope (SEM) image, and dividing the total of each by the number of measurements (100 pieces).
  • SEM scanning electron microscope
  • the glass fiber having a flat cross-sectional shape may be, for example, a pulverized product of the glass fiber having a flat cross-sectional shape.
  • the glass fiber having a flat cross-sectional shape is a pulverized product of the glass fiber having a flat cross-sectional shape may be described as an example.
  • the glass base material in the present embodiment may be any glass fiber having the above-mentioned shape characteristics, and is not limited to the pulverized product of the glass fiber.
  • a crushed product of glass fiber having a flat cross-sectional shape may be referred to as "flat cross-sectional glass milled fiber”.
  • the length L1 corresponding to the minor axis and the length L2 corresponding to the major axis in the flat cross section of the glass fiber are defined as “minor axis L1 of the glass substrate” and “major axis of the glass substrate, respectively”. It may be described as "L2”.
  • the length L3 corresponding to the fiber length of the glass fiber may be described as "the length L3 of the glass base material”.
  • the glass filler of the present embodiment contains, for example, a flat cross-section glass milled fiber as a glass base material.
  • the glass substrate has the above-mentioned shape characteristics, that is, (L2 average value) / (L1 average value) of 1.5 or more and 8 or less, L1 average value of 1.0 ⁇ m or more and 10 ⁇ m or less, and L3 average.
  • the shape is controlled so that the value satisfies 80 ⁇ m or more and 160 ⁇ m or less. Since the average value of the length L3 of the glass base material is 80 ⁇ m or more and 160 ⁇ m or less, the glass base material can exhibit the function as a fiber.
  • the glass base material can realize the effect of imparting sufficiently high mechanical strength to the resin molded product, which is similar to the effect when the glass fiber is used as the filler.
  • the minor axis L1 and the major axis L2 of the glass substrate have (average value of L2) / (average value of L1) of 1.5 or more and 8 or less, and the average value of L1 is 1.0 ⁇ m or more.
  • the standard deviation of the variation of L1 and L2 is preferably small, and is preferably 25% or less with respect to the average value of L1 and L2, respectively. It is preferable that the standard deviation of L3 is also smaller.
  • the glass filler of the present embodiment further includes a coating film that covers at least a part of the surface of the glass substrate, in addition to using a glass substrate that satisfies the above-mentioned shape characteristics.
  • This coating film contains a surface treatment agent containing a silane coupling agent, and is contained in a proportion of 0.05% by mass or more and 2.5% by mass or less with respect to the entire glass filler of the present embodiment. ..
  • the glass filler of the present embodiment has a structure in which a glass base material having a specific shape is coated with a coating film containing a surface treatment agent, so that the glass filler has a conventional circular cross-sectional shape.
  • a glass base material having a specific shape is coated with a coating film containing a surface treatment agent, so that the glass filler has a conventional circular cross-sectional shape.
  • the fiber or the conventional glass milled fiber having a flat cross-sectional shape is used as the resin reinforcing filler, it is possible to realize a resin molded product having both high mechanical strength and excellent dimensional stability.
  • the average value of the minor axis L1 of the glass substrate is 1.0 ⁇ m or more and 10 ⁇ m or less.
  • the average value of the minor axis L1 of the glass substrate is, for example, preferably 1.5 ⁇ m or more, and more preferably 2.0 ⁇ m or more.
  • the average value of the minor axis L1 of the glass substrate is, for example, preferably 9.0 ⁇ m or less, and more preferably 8.0 ⁇ m or less.
  • the average value of the major axis L2 of the glass substrate may be determined so that (average value of L2) / (average value of L1) satisfies 1.5 or more and 8 or less, and is not particularly limited.
  • the average value of the major axis L2 of the glass substrate is, for example, preferably 3.0 ⁇ m or more, and more preferably 5.0 ⁇ m or more.
  • the average value of the major axis L2 of the glass substrate is, for example, preferably 50 ⁇ m or less, and more preferably 30 ⁇ m or less.
  • the ratio of the average value of the major axis L2 to the average value of the minor axis L1 of the glass substrate (average value of L2) / (average value of L1) is 1.5 or more and 8 or less as described above.
  • (Average value of L2) / (average value of L1) is preferably 2.0 or more, more preferably 2.5 or more, for example.
  • (average value of L2) / (average value of L1) is preferably 7.0 or less, more preferably 6.0 or less, for example.
  • the average value of the length L3 of the glass substrate is 80 ⁇ m or more and 160 ⁇ m or less.
  • the average value of the length L3 of the glass substrate is, for example, preferably 90 ⁇ m or more, and more preferably 100 ⁇ m or more.
  • the average value of the length L3 of the glass substrate is longer than 160 ⁇ m, the fibers are entangled with each other to form a fluffy shape.
  • the glass filler of the present embodiment can further improve the dimensional stability while maintaining the mechanical strength of the resin molded product.
  • composition of the glass base material a generally known composition of glass can be used. Specifically, glass having a small amount of alkali metal oxide such as E glass can be preferably used.
  • a typical composition of E-glass (the glass composition of the first example) is shown below. That is, the glass substrate may contain the glass composition of the first example. The unit of composition below is mass%.
  • the glass base material may contain a glass composition having the following composition (example of the glass composition of the second example) as a glass composition having a small amount of alkali metal oxide.
  • the glass composition of the second example is expressed in% by mass. 59 ⁇ SiO 2 ⁇ 65, 8 ⁇ Al 2 O 3 ⁇ 15, 47 ⁇ (SiO 2- Al 2 O 3 ) ⁇ 57, 1 ⁇ MgO ⁇ 5, 20 ⁇ CaO ⁇ 30, 0 ⁇ (Li 2 O + Na 2 O + K 2 O) ⁇ 2, 0 ⁇ TiO 2 ⁇ 5, B 2 O 3 , F, ZnO, BaO, SrO, ZrO 2 are substantially not contained.
  • the glass composition is disclosed by Applicants in WO 2006/068255.
  • substantially not contained means that it is not intentionally contained except, for example, when it is unavoidably mixed by an industrial raw material.
  • the content of each of B 2 O 3 , F, ZnO, BaO, SrO and ZrO 2 is less than 0.1% by mass (preferably less than 0.05% by mass, more preferably 0.03% by mass). Less than).
  • the glass substrate may contain the following glass composition (the glass composition of the third example).
  • the glass composition of the third example is represented by mass%. 50 ⁇ SiO 2 ⁇ 54 25 ⁇ B 2 O 3 ⁇ 30 12 ⁇ Al 2 O 3 ⁇ 15 0.5 ⁇ MgO ⁇ 1.9 3.0 ⁇ CaO ⁇ 5.5 0 ⁇ ZnO ⁇ 3.5 0.1 ⁇ Li 2 O ⁇ 0.5 0.1 ⁇ Na 2 O ⁇ 0.3
  • the dielectric constant of the glass composition at a frequency of 1 MHz is less than 5.0.
  • the glass composition of the third example is a low dielectric constant glass composition. Therefore, when the glass substrate is formed by the glass composition of the third example, the glass filler of the present embodiment is a resin reinforcing material for applications requiring a low dielectric constant, for example, a printed wiring board and a communication device component. Can be used for. Further, in the glass composition of the third example, when spinning into glass fibers, devitrification is less likely to occur even when the fiber diameter of the glass fibers is small, and mixing of bubbles is suppressed. Therefore, when the glass base material is formed by the glass composition of the third example, the performance as the original glass base material is not impaired due to the occurrence of devitrification and the mixing of bubbles, so that the glass of the present embodiment is not impaired. The reliability of the filler is improved.
  • the glass substrate may contain the following glass composition (the glass composition of the fourth example).
  • the glass composition of the fourth example is expressed in% by mass. 50 ⁇ SiO 2 ⁇ 56 20 ⁇ B 2 O 3 ⁇ 30 10 ⁇ Al 2 O 3 ⁇ 20 3.5 ⁇ MgO + CaO ⁇ 10 0 ⁇ R 2 O ⁇ 1.0
  • the glass composition contains Fe 2 O 3 and the dielectric constant of the glass composition at a frequency of 1 MHz is less than 5.0.
  • R 2 O is at least one oxide selected from the group consisting of Li 2 O, Na 2 O and K 2 O.
  • the glass composition of the fourth example is a low dielectric constant glass composition. Therefore, when the glass substrate is formed by the glass composition of the fourth example, the glass filler of the present embodiment is a resin reinforcing material for applications requiring a low dielectric constant, for example, a printed wiring board and a communication device component. Can be used for. Further, according to the glass composition of the fourth example, even when the fiber diameter of the glass fiber to be formed is small, the occurrence of yarn breakage during spinning is suppressed, and the yarn breakage of the glass fiber during processing and the yarn breakage during processing are suppressed. Occurrence of fluffing is suppressed. Therefore, when the glass base material is formed by the glass composition of the fourth example, the performance as the original glass base material is not impaired due to the occurrence of thread breakage and fluffing, and therefore, the glass filler of the present embodiment Improves reliability.
  • the glass substrate may contain the following glass composition (the glass composition of the fifth example).
  • the glass composition of the fifth example is represented by mass%. 40 ⁇ SiO 2 ⁇ 60 25 ⁇ B 2 O 3 ⁇ 45 5 ⁇ Al 2 O 3 ⁇ 15 0 ⁇ R 2 O ⁇ 5 0 ⁇ RO ⁇ 15 Contains the ingredients of.
  • the glass composition of the fifth example satisfies SiO 2 + B 2 O 3 ⁇ 80 and / or SiO 2 + B 2 O 3 ⁇ 78 and 0 ⁇ RO ⁇ 10.
  • R 2 O is at least one oxide selected from the group consisting of Li 2 O, Na 2 O and K 2 O
  • RO is MgO, CaO and SrO. It is at least one oxide selected from the group consisting of.
  • the glass composition of the fifth example is a low dielectric constant glass composition. Therefore, when the glass substrate is formed by the glass composition of the fifth example, the glass filler of the present embodiment is a resin reinforcing material for applications requiring a low dielectric constant, for example, a printed wiring board and a communication device component. Can be used for. Further, since the glass composition of the fifth example is a glass composition suitable for mass production, mass production of the glass filler of the present embodiment becomes easy.
  • the temperature T2 becomes viscosity 10 2 dPas is 1700 ° C. or less.
  • the glass substrate may contain the following glass composition (the glass composition of the sixth example).
  • the glass composition of the sixth example is represented by mass%. 40 ⁇ SiO 2 ⁇ 60 25 ⁇ B 2 O 3 ⁇ 45 0 ⁇ Al 2 O 3 ⁇ 18 0 ⁇ R 2 O ⁇ 5 0 ⁇ RO ⁇ 12 Contains the ingredients of.
  • R 2 O is at least one oxide selected from the group consisting of Li 2 O, Na 2 O and K 2 O, and RO is MgO, CaO and SrO. It is at least one oxide selected from the group consisting of.
  • the glass composition of the sixth example is a low dielectric constant glass composition. Therefore, when the glass substrate is formed by the glass composition of the sixth example, the glass filler of the present embodiment is a resin reinforcing material for applications requiring a low dielectric constant, for example, a printed wiring board and a communication device component. Can be used for. Further, since the glass composition of the sixth example is a glass composition suitable for mass production, mass production of the glass filler of the present embodiment becomes easy.
  • the temperature T2 becomes viscosity 10 2 dPas is 1700 ° C. or less.
  • the glass substrate may contain the following glass composition (the glass composition of the seventh example).
  • the glass composition of the seventh example is represented by mass%. 40 ⁇ SiO 2 ⁇ 60 25 ⁇ B 2 O 3 ⁇ 45 0 ⁇ Al 2 O 3 ⁇ 18 0 ⁇ R 2 O ⁇ 5 3 ⁇ RO ⁇ 8 Contains the ingredients of.
  • SiO 2 + B 2 O 3 ⁇ 75, and SiO 2 + B 2 O 3 + Al 2 O 3 ⁇ 97 Is established.
  • R 2 O is at least one oxide selected from the group consisting of Li 2 O, Na 2 O and K 2 O
  • RO is MgO, CaO and SrO. It is at least one oxide selected from the group consisting of.
  • the glass composition of the seventh example is a low dielectric constant glass composition. Therefore, when the glass substrate is formed by the glass composition of the seventh example, the glass filler of the present embodiment is a resin reinforcing material for applications requiring a low dielectric constant, for example, a printed wiring board and a communication device component. Can be used for. Further, since the glass composition of the seventh example is a glass composition suitable for mass production, mass production of the glass filler of the present embodiment becomes easy.
  • the glass substrate may contain the following glass composition (the glass composition of the eighth example).
  • the glass composition of the eighth example SiO 2 + B 2 O 3 ⁇ 77 is established in terms of mass%.
  • a dielectric constant of 4.4 or less in the frequency 1 GHz, and the temperature T2 becomes viscosity 10 2 dPas is 1700 ° C. or less.
  • the glass composition of the eighth example is a low dielectric constant glass composition. Therefore, when the glass substrate is formed by the glass composition of the eighth example, the glass filler of the present embodiment is a resin reinforcing material for applications requiring a low dielectric constant, for example, a printed wiring board and a communication device component. Can be used for. Further, since the glass composition of the eighth example is a glass composition suitable for mass production, mass production of the glass filler of the present embodiment becomes easy.
  • the glass substrate may contain the following glass composition (the glass composition of the ninth example).
  • the glass composition of the ninth example is represented by mass%. 95 ⁇ SiO 2 ⁇ 99.5 0 ⁇ B 2 O 3 ⁇ 2 0.01 ⁇ Al 2 O 3 ⁇ 4 0 ⁇ R 2 O ⁇ 4 0.01 ⁇ RO' ⁇ 4 0 ⁇ TiO 2 ⁇ 4 Contains the ingredients of.
  • R 2 O is at least one oxide selected from the group consisting of Li 2 O, Na 2 O and K 2 O, and RO'is MgO, CaO, It is at least one oxide selected from the group consisting of SrO and ZnO.
  • the glass composition of the ninth example is a low dielectric constant glass composition. Therefore, when the glass substrate is formed by the glass composition of the ninth example, the glass filler of the present embodiment is a resin reinforcing material for applications requiring a low dielectric constant, for example, a printed wiring board and a communication device component. Can be used for.
  • a method for manufacturing a glass base material will be described.
  • an example of a method for manufacturing a glass base material will be described by taking as an example a case where the glass base material is a flat cross-section glass milled fiber.
  • the minor axis of the fiber cross section is the same as the minor axis L1 of the above-mentioned glass base material, and the major axis of the fiber cross section is the same as the major axis L2 of the above-mentioned glass substrate. Omit.
  • the glass fiber having a flat cross-sectional shape can be produced by using a known production method of the glass fiber having a flat cross-sectional shape, for example, as described in Japanese Patent Application Laid-Open No. 6-228806.
  • a nozzle for flat cross-section glass fiber spinning provided with a plurality of convex edges extending downward from the outer peripheral tip of a nozzle tip having a single or a plurality of orifice holes.
  • a glass fiber having a cross-sectional shape of a desired shape and size can be produced. That is, by adjusting the shape and size of the nozzle tip, the average value of the minor axis L1 and the average value of the major axis L2 of the glass substrate can be set to desired values.
  • the obtained glass fiber is crushed with, for example, a ball mill.
  • a flat cross-section glass milled fiber can be obtained.
  • the length L3 of the obtained glass base material can be adjusted by changing the crushing conditions of the glass fibers.
  • the adjustment of the glass fiber of a predetermined length is not limited to ball mill pulverization, and other methods or a plurality of methods can be used in combination. For example, impact crusher, gyre crusher, cone crusher, jaw crusher, roll crusher, cutter mill, self-crushing machine, stamp mill, stone mill, squirrel machine, ring mill, roller mill, jet mill, hammer mill, pin mill, rotary mill.
  • a vibration mill, a planetary mill, an attritor, or a bead mill can be used alone, or these methods can be used in combination as appropriate to produce the glass substrate according to the present embodiment.
  • other crushing methods such as flame flow crushing (burner crushing) and / or spray crushing (high pressure gas crushing) may be used. ..
  • the coating film covers at least a part of the surface of the glass substrate.
  • the coating film is used. , It is preferable to cover the entire surface of the glass substrate.
  • the coating film contains a surface treatment agent including a silane coupling agent.
  • the coating film is preferably composed of a surface treatment agent substantially, and may be composed of only the surface treatment agent.
  • the fact that the coating film is substantially composed of a surface treatment agent means that the surface treatment agent contained in the coating film is 70% by mass or more, and preferably 80% by mass or more.
  • the coating film may contain inorganic fine particles such as silica fine particles in addition to the surface treatment agent.
  • silane coupling agent examples include ⁇ -aminopropyltriethoxysilane, ⁇ -aminopropyltrimethoxysilane, bis (3-triethoxysilylpropyl) amine, ⁇ -ureidopropyltriethoxysilane, and ⁇ -glycidoxypropyl. Examples thereof include trimethoxysilane, vinyltriethoxysilane, and ⁇ -methacryloxypropyltrimethoxysilane.
  • the silane coupling agent preferably has an amino group or a glycidyl group.
  • the surface treatment agent contains a silane coupling agent having an amino group or a glycidyl group
  • the compatibility of the glass and the matrix resin with each other is improved as compared with the case where the surface treatment agent contains other silane coupling agents, and silane.
  • the coupling agent reacts with the glass and the matrix resin to improve the adhesion between the glass filler and the matrix resin at the interface. Therefore, among the silane coupling agents exemplified above, ⁇ -aminopropyltriethoxysilane, ⁇ -aminopropyltrimethoxysilane, bis (3-triethoxysilylpropyl) amine, and ⁇ -glycidoxypropyltrimethoxysilane. Is preferably used.
  • a titanium-based coupling agent, an aluminum-based coupling agent, a zirconia-based coupling agent, or the like can also be used.
  • the surface treatment agent may further contain a resin.
  • the resin contained in the surface treatment agent is not particularly limited, but for example, a glycidyl group-containing resin or a urethane resin is preferably used. That is, the resin contained in the surface treatment agent may contain a glycidyl group-containing resin or a urethane resin.
  • the surface treatment agent contains a glycidyl group-containing resin, a reaction between the glycidyl group and the matrix resin can be expected. Since the surface treatment agent contains the urethane resin, high compatibility between the urethane resin and the matrix resin can be expected, and further, improvement in the adhesion at the interface between the glass filler and the matrix resin can be expected.
  • Examples of the glycidyl group-containing resin include bisphenol A type epoxy resin, bisphenol F type epoxy resin, bisphenol AD type epoxy resin, phenol novolac type epoxy resin, O-cresol novolac type epoxy resin, and hydrogenated bisphenol A type epoxy resin. Can be mentioned.
  • Urethane resin is a polymer composed of a copolymer of a polyol component and a polyisocyanate component.
  • the polyisocyanate component includes an aliphatic, an alicyclic, an aromatic, and an aromatic aliphatic, and is not particularly limited.
  • hexamethylene diisocyanate is preferably used.
  • isophorone diisocyanate and hydrogenated xylylene diisocyanate are preferably used.
  • the polyol component includes, but is not limited to, a polyether polyol, a polyester polyol, a polytetramethylene glycol, a polybutadiene polyol, a polyisoprene polyol, an amine polyol, castor oil and a derivative thereof.
  • the glycidyl group-containing resin or the urethane resin may be used independently. That is, the resin contained in the surface treatment agent may be only the glycidyl group-containing resin or only the urethane resin. Further, as the resin contained in the surface treatment, a plurality of types of resins may be used in combination. For example, a glycidyl group-containing resin or a urethane resin may be used in combination with another resin, or a glycidyl group-containing resin and a urethane resin may be used in combination.
  • the surface treatment agent may further contain a cross-linking agent, a surfactant, and / or a lubricant in addition to the silane coupling agent and the resin.
  • the surface treatment agent preferably contains, for example, 0.1% by mass or more, more preferably 1.0% by mass or more, and further preferably 5.0% by mass or more of the silane coupling agent.
  • the glass filler of the present embodiment can further improve the dimensional stability of the resin molded product.
  • the surface treatment agent may consist only of a silane coupling agent. That is, in the surface treatment agent, the silane coupling agent may be 100% by mass.
  • the surface treatment agent may or may not contain a resin.
  • the surface treatment agent preferably contains, for example, 30% by mass or more, and more preferably 40% by mass or more of the resin. Further, the surface treatment agent preferably contains, for example, 99.9% by mass or less, and more preferably 95% by mass or less of the resin.
  • the glass filler of the present embodiment can further improve the dimensional stability of the resin molded product.
  • the coating film may be prepared using a solution containing a coating film material containing a surface treatment agent, for example, as described later.
  • a solution containing a coating film material containing a surface treatment agent for example, as described later.
  • an emulsion may be used as the resin.
  • the amount of surfactant required for emulsification may be contained within a range that does not affect the properties of the resin.
  • about 1 to 10% by mass of a surfactant may be added based on the mass of the resin.
  • the content ratio of the coating film is 0.05% by mass or more and 2.5% by mass or less.
  • the glass filler of the present embodiment can suppress the occurrence of warpage of the resin molded product and can realize higher dimensional stability.
  • the coating film is preferably contained in an amount of 0.08% by mass or more based on the entire glass filler.
  • the content ratio of the coating film is 0.08% by mass or more, the surface of the glass substrate can be sufficiently covered with the coating film. Therefore, the glass filler of the present embodiment can further improve the mechanical strength of the resin molded product and also improve the dimensional stability.
  • the coating film is preferably contained in an amount of 2.0% by mass or less based on the entire glass filler.
  • the content ratio of the coating film is 2.0% by mass or less, the bonding force between the glass fillers does not become too strong, so that the glass filler is uniformly dispersed in the resin molded product and the mechanical strength of the resin molded product is obtained. Can be improved. Further, since each component of the coating film does not become excessive and hinders the adhesion between the glass filler and the matrix resin, the dimensional stability of the resin molded product is further improved.
  • the method of coating the surface of the glass substrate with the coating film is not particularly limited, and a known method can be used.
  • a solution containing a coating film material containing a surface treatment agent (coating film material solution) is added to a glass substrate, stirred, and dried to cover at least a part of the surface of the glass substrate.
  • a glass filler coated with a film can be formed.
  • Specific methods for adding, stirring, and drying the coating film material solution are not particularly limited, but examples thereof will be described below.
  • a predetermined amount of a coating film material solution is added by spraying or the like while flowing a glass base material, and the mixture is stirred and stirred. To do.
  • the glass base material to which the coating film material solution is attached is dried while stirring in the mixer, or the glass base material to which the coating film material solution is attached is taken out from the mixer and dried.
  • a glass filler in which a glass base material is coated with a coating film can also be produced by using a rolling granulation method as described in JP-A No. 2-124732. That is, a glass base material may be placed in a horizontal vibration type granulator provided with stirring blades, and a coating film material solution may be sprayed onto the glass substrate for granulation.
  • glass in which the glass substrate is coated with a coating film by applying known methods generally called agitation granulation method, fluidized bed granulation method, injection granulation method and rotary granulation method. Fillers can be made.
  • the drying step is carried out, for example, by heating the glass substrate to which the coating film material solution is attached to a temperature equal to or higher than the boiling point of the solvent used in the coating film material solution and drying until the solvent volatilizes. It is said.
  • the content ratio of the coating film in the glass filler can be controlled by adjusting the concentration of the coating film material in the coating film material solution to be added or sprayed. That is, by adding or spraying a predetermined amount of the coating film material solution to a predetermined amount of the glass base material so that the coating film material has a predetermined amount, the content ratio of the coating film becomes a predetermined value.
  • Glass filler can be manufactured.
  • the resin composition of the present embodiment contains the glass filler of the present embodiment as described above and the matrix resin. Since the resin composition of the present embodiment contains the glass filler of the present embodiment, it is possible to realize a resin molded product having both high mechanical strength and excellent dimensional stability.
  • the matrix resin is not particularly limited, and may be a thermoplastic resin or a thermosetting resin.
  • thermosetting resin examples include epoxy resin, phenol resin, unsaturated polyester resin, urea resin, melamine resin, diallyl phthalate resin, silicon resin, vinyl ester resin, polyurethane resin, polyimide resin, bismaleimide resin, and thermosetting resin.
  • examples thereof include acrylic resins and mixed and cured resins thereof.
  • thermoplastic resin examples include At least one selected from the group consisting of polyolefins, polyesters, polycarbonates, polyvinyl chlorides, polystyrenes, polyamides, polyphenylene sulfides, polyphenylene ethers, polyetherketones, acrylic resins and liquid crystal polymers.
  • Copolymers or polymer alloys comprising at least two selected from the group consisting of polyolefins, polyesters, polycarbonates, polyvinyl chlorides, polystyrenes, polyamides, polyphenylene sulfides, polyphenylene ethers, polyether ketones, acrylic resins and liquid crystal polymers. Can be mentioned.
  • polyolefins examples include polybutylene, polypropylene, polyethylene and the like.
  • polyesters include thermoplastic polyesters such as polybutylene terephthalate.
  • polyamide examples include polyamide 66 and the like.
  • polyetherketones examples include polyetheretherketones and the like.
  • acrylic resins include polymethylmethacrylate and the like.
  • the resin composition of the present embodiment is more likely to realize a resin molded product having high mechanical strength and dimensional stability.
  • the thermoplastic resin may contain a polyamide (for example, polyamide 66), a thermoplastic polyester (for example, polybutylene terephthalate), and / or polycarbonate.
  • the resin composition of the present embodiment has a high reinforcing effect and a dimensional stabilizing effect on the matrix resin of the glass filler of the present embodiment, particularly when polyamide, thermoplastic polyester, and / or polycarbonate is used as the matrix resin. Therefore, it is easier to realize a resin molded product having high mechanical strength and excellent dimensional stability.
  • the content ratio of the glass filler in the resin composition is preferably 10% by mass or more and 70% by mass or less.
  • the content is 10% by mass or more, the function of the glass filler as a reinforcing material can be fully exhibited.
  • the content is 70% by mass or less, the glass filler can be uniformly dispersed in the resin composition.
  • it is more preferable that the content of the glass filler is 15% by mass or more and 60% by mass or less.
  • the resin composition may contain components other than the matrix resin and the glass filler.
  • other components include fillers such as carbon black and thermoplastic elastomers.
  • Thermoplastic elastomers include olefin-based elastomers, styrene-based elastomers, hydrogenated polymer-based elastomers, and the like.
  • the olefin-based elastomer include ethylene / ⁇ -olefin copolymer elastomer (ethylene / propylene copolymer elastomer (EPR), ethylene / butene copolymer elastomer (EBR), and ethylene / hexene copolymer elastomer (EHR)).
  • Ethylene / octene copolymer elatomer EOR
  • ethylene / ⁇ -olefin / diene ternary copolymer elastomer ethylene / propylene / ethylidene norbornene copolymer, ethylene / propylene / butadiene copolymer, ethylene / (Propylene / isoprene copolymer, etc.
  • Two or more types of thermoplastic elastomers can be used in combination.
  • Example 1 Glass substrate
  • E-glass was placed in a melting tank heated to 1200 ° C. or higher to melt it.
  • Glass fibers were produced by flowing out the obtained molten glass from a nozzle tip for spinning glass fiber having a flat cross section having a shape as shown in FIG. 4 of JP-A-6-228806.
  • the obtained glass fiber had a flat cross-sectional shape having a minor axis of 7 ⁇ m and a major axis of 28 ⁇ m.
  • the obtained glass fiber was pulverized with a ball mill to prepare a flat cross-section glass milled fiber, which was used as a glass base material.
  • the minor axis L1 and the major axis L2 of the glass substrate were the same as the minor axis 7 ⁇ m and the major axis 28 ⁇ m of the glass fiber before pulverization, respectively. That is, when the minor axis L1 and the major axis L2 of the cross section of the obtained glass substrate were measured using SEM images of the cross sections of any 100 glass substrates, the minor axis L1 was 7 ⁇ m and the major axis L2. Was 28 ⁇ m. Therefore, in the glass substrate of this example, the average value of the minor axis L1 was 7 ⁇ m, and the average value of the major axis L2 was 28 ⁇ m.
  • the length L3 of any 500 glass substrates was measured using an optical microscope image of the glass substrate. Using the obtained measurement results, the number average length of the length L3 of the glass substrate was determined. The number average length of the length L3 of the glass substrate was 145 ⁇ m.
  • the surface treatment agent solution contains a glycidyl group-containing resin as a resin (so-called epoxy resin, specifically, a solid phenol novolac type epoxy resin) as a component constituting the surface treatment agent (solid content), and a silane coupling agent. ⁇ -Aminopropyltriethoxysilane and was contained. In addition, water was used as the solvent for the surface treatment agent solution.
  • the glass base material (undried) to which the surface treatment agent solution was attached was taken out from the mixer and dried at 125 ° C. for 8 hours in a dryer to obtain the glass filler of Example 1.
  • the liquid preparation was water-based in this example, an emulsion was used as the resin. That is, the resin used contained a surfactant (2% by mass) that did not affect the properties of the resin for emulsification.
  • the content ratio of the coating film in the obtained glass filler was examined by the ignition loss method. Specifically, an appropriate amount of the glass filler was dried at 110 ° C. and then heated in an atmosphere of 625 ° C. to remove the coating film from the surface of the glass filler. The content ratio of the coating film in the glass filler was calculated from the difference between the mass of the glass filler before heating and the mass of the glass filler after heating (that is, the mass of the glass substrate). That is, in the coating film, the glycidyl group-containing resin was 50% by mass and the silane coupling agent was 50% by mass. The results are shown in Table 2.
  • the maximum tensile strength and Izod impact strength were measured as the mechanical strength of the resin molded product.
  • the maximum tensile strength was measured according to JIS K 7113.
  • the Izod impact strength was measured according to JIS K 711-1. The measurement results are shown in Table 2.
  • the dimensional stability of the resin molded product was evaluated by measuring the amount of warpage of the resin molded product.
  • a resin molded product for measuring warpage a flat plate of 30 mm square and 0.5 mm in thickness was molded, and the flat plates were placed on a flat surface for the five obtained flat plates, and when a certain point was supported, the flat plate was formed. The upper support point and the position where the flat plate had the largest warp were searched for, and the distance was measured. The average value of the measured values of the five sheets was taken as the amount of warpage.
  • the measurement results are shown in Table 2.
  • the resin composition was visually observed for stains and cloudiness of the mold after 20 injection moldings were performed continuously, and the degree of stain was evaluated.
  • This mold stain is affected by the proportion of the coating film in the glass filler, that is, the amount of organic matter attached and the type of surface treatment agent material, and the organic matter in the coating film is decomposed by the heating from the molding machine and the frictional heat during kneading. This is caused by the fact that it is likely to occur, especially when the proportion of the coating film is high.
  • Table 2 the case where the mold is dirty is shown as x, the case where the mold is hardly dirty is shown as ⁇ , and the case where the mold is not dirty is shown as ⁇ .
  • Example 2 to 4 The glass fillers of Examples 2 to 4 were prepared in the same manner as in Example 1 except that the concentration of the surface treatment agent in the surface treatment agent solution was changed. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 1 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 2.
  • Example 5 The glass filler of Example 5 was prepared by the same method as in Example 1 except that the crushing conditions of the glass fibers were changed and the number average length of the length L3 of the glass substrate was changed to 110 ⁇ m. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 1 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 2.
  • Example 6 The glass filler of Example 6 was prepared by the same method as in Example 1 except that the resin of the surface treatment agent, that is, the resin in the coating film was changed from the glycidyl group-containing resin to the urethane resin. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 1 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 2.
  • Examples 7 and 8 The same method as in Example 1 except that the surface treatment agent is composed of only the silane coupling agent, that is, the coating film is composed of only the silane coupling agent, and the concentration of the surface treatment agent in the surface treatment agent solution is changed.
  • the glass fillers of Examples 7 and 8 were obtained. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 1 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 2.
  • Example 9 The silane coupling agent for the coating film was prepared in the same manner as in Example 7 except that the silane coupling agent for the surface treatment agent was changed from ⁇ -aminopropyltriethoxysilane to 3-glycidoxypropyltrimethoxysilane. A glass filler of Example 9 different from the coating film of Example 7 was obtained. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 1 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 2.
  • Example 10 In Example 1, a nozzle tip for spinning glass fiber having a flat cross section and spinning conditions were adjusted to produce a glass fiber having a flat cross-sectional shape having a minor axis of 10 ⁇ m and a major axis of 25 ⁇ m. This was pulverized with a ball mill to prepare a flat cross-section glass milled fiber having a number average length of a glass substrate length L3 of 160 ⁇ m, and this was used as a glass substrate. The minor axis L1 and the major axis L2 of the glass substrate were the same as the minor axis 10 ⁇ m and the major axis 25 ⁇ m of the glass fiber before pulverization, respectively.
  • Example 2 the surface treatment was carried out in the same manner as in Example 1 to obtain the glass filler of Example 10. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 1 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 2.
  • Example 1 A glass substrate was prepared in the same manner as in Example 1. The glass substrate was used as the glass filler of Comparative Example 1 without surface treatment on the glass substrate, that is, without forming a coating film. A resin composition was prepared in the same manner as in Example 1 and a resin molded product was obtained. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 3.
  • Comparative Examples 2 and 3 The glass fillers of Comparative Examples 2 and 3 were prepared in the same manner as in Example 1 except that the concentration of the surface treatment agent in the surface treatment agent solution was changed. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 1 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 3.
  • Comparative Example 4 The glass filler of Comparative Example 4 was prepared by the same method as in Example 1 except that the crushing conditions of the glass fibers were changed and the number average length of the length L3 of the glass substrate was changed to 50 ⁇ m. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 1 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 3.
  • Comparative Example 5 Using the E glass having the composition shown in Table 1 used for producing the glass substrate of Example 1, a circular cross-section glass fiber having a diameter of 11 ⁇ m was produced by a known spinning method. This glass fiber was pulverized with a ball mill to prepare a glass base material of Comparative Example 5 in which the number average length of the length L3 of the glass base material was 75 ⁇ m. In Comparative Example 5, the glass substrate was used as the glass filler of Comparative Example 5 without surface treatment on the glass substrate, that is, without forming a coating film. A resin composition was prepared in the same manner as in Example 1 and a resin molded product was obtained. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 3.
  • Example 6 A coating film was formed on the glass substrate of Comparative Example 5 using the same surface treatment agent solution as in Example 7 to obtain a glass filler of Comparative Example 6. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 1 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 3.
  • Example 7 A coating film was formed on the glass substrate of Comparative Example 5 using the same surface treatment agent solution as in Example 8 to obtain a glass filler of Comparative Example 7. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 1 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 3.
  • Example 8 A coating film was formed on the glass substrate of Comparative Example 5 using the same surface treatment agent solution as in Example 1 to obtain a glass filler of Comparative Example 8. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 1 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 3.
  • Comparative Example 13 A glass filler of Comparative Example 13 was obtained in the same manner as in Example 1 except that the glass substrate of Example 1 was changed to a flake-shaped glass substrate (average particle size: 160 ⁇ m, average thickness: 5 ⁇ m). Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 1 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 3.
  • Comparative Example 14 A glass filler of Comparative Example 14 was obtained in the same manner as in Example 1 except that the glass substrate of Example 1 was changed to a flake-shaped glass substrate (average particle size: 160 ⁇ m, average thickness: 0.7 ⁇ m). .. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 1 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 3.
  • Example 15 A glass fiber having a flat cross-sectional shape was produced by the same method as in Example 1. The glass fiber was pulverized with a ball mill to obtain a glass substrate having a length L3 of the glass substrate and a number average length of 200 ⁇ m. This glass base material was used as the glass base material of Comparative Example 15, but the fibers were entangled with each other and became fluffy. The glass substrate was surface-treated using the same surface treatment agent solution as in Example 1, but the surface treatment agent solution did not penetrate into the inside and became solidified on the surface of the fluff ball. Therefore, the production of the resin composition was abandoned.
  • Example 16 A glass substrate was prepared in the same manner as in Example 10. The glass substrate was used as the glass filler of Comparative Example 16 without surface treatment on the glass substrate, that is, without forming a coating film. A resin composition was prepared in the same manner as in Example 1 and a resin molded product was obtained. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 3.
  • Example 11 The point that the surface treatment agent solution in which the ratio of the silane coupling agent and the glycidyl group-containing resin in the coating film was changed as shown in Table 4 was used, and the type of the glycidyl group-containing resin was changed from the solid phenol novolac type.
  • the glass filler of Example 11 was prepared in the same manner as in Example 1 except that it was changed to the solid bisphenol A type. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, both were uniformly mixed so that the glass filler of Example 10 was 30% by mass and the polycarbonate (Iupilon S3000F manufactured by Mitsubishi Engineering Plastics Co., Ltd.) was 70% by mass.
  • the obtained mixture was kneaded with an extrusion molding machine (manufactured by Technobel Co., Ltd., KZW15-30MG, temperature: about 270 to 280 ° C.) to obtain a resin composition containing polycarbonate as a matrix resin and a glass filler.
  • This resin composition was molded by an injection molding machine (HM7 manufactured by Nissei Resin Industry Co., Ltd.) to obtain a resin molded product.
  • the content of the glass filler in the obtained resin molded product was 30% by mass.
  • Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 4.
  • Example 12 The same method as in Example 11 except that the surface treatment agent is composed of only the silane coupling agent, that is, the coating film is composed of only the silane coupling agent, and the concentration of the surface treatment agent in the surface treatment agent solution is changed.
  • the glass filler of Example 12 was obtained. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 11 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 4.
  • Example 17 A glass substrate was prepared in the same manner as in Example 1. The glass substrate was used as the glass filler of Comparative Example 17 without surface treatment on the glass substrate, that is, without forming a coating film. A resin composition was prepared in the same manner as in Example 11 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 4.
  • the resin molded products of Examples 11 and 12 have a smaller amount of warpage than the resin molded products of Comparative Example 17 in which a glass filler having no coating film is used, and have tensile strength and tensile strength.
  • the impact strength was high. That is, as compared with the glass filler of Comparative Example 17, the glass fillers of Examples 11 and 12 have both high mechanical strength and excellent dimensional stability in the molded product of the resin when blended with the resin. I was able to grant it.
  • Example 13 The glass of Example 13 in the same manner as in Example 1 except that a surface treatment agent solution was used in which the ratio of the silane coupling agent and the glycidyl group-containing resin in the coating film was changed as shown in Table 5. A filler was prepared. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, both were uniformly mixed so that the glass filler of Example 13 was 30% by mass and the polybutylene terephthalate (Duranex 2000 manufactured by Polyplastics Co., Ltd.) was 70% by mass.
  • a surface treatment agent solution was used in which the ratio of the silane coupling agent and the glycidyl group-containing resin in the coating film was changed as shown in Table 5.
  • a filler was prepared. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, both were uniformly mixed so that the glass filler of Example 13 was 30% by mass and the polybutylene terephthalate (Duranex
  • the obtained mixture is kneaded with an extrusion molding machine (manufactured by Technobel Co., Ltd., KZW15-30MG, temperature: about 250 to 270 ° C.) to obtain a resin composition containing polybutylene terephthalate as a matrix resin and a glass filler. It was.
  • This resin composition was molded by an injection molding machine (HM7 manufactured by Nissei Resin Industry Co., Ltd.) to obtain a resin molded product.
  • the content of the glass filler in the obtained resin molded product was 30% by mass.
  • Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 5.
  • Example 14 The glass filler of Example 14 was prepared in the same manner as in Example 13 except that the resin of the surface treatment agent, that is, the resin in the coating film was changed from the glycidyl group-containing resin to the urethane resin. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 13 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 5.
  • Examples 15 and 16 The same method as in Example 13 except that the surface treatment agent is composed of only the silane coupling agent, that is, the coating film is composed of only the silane coupling agent, and the concentration of the surface treatment agent in the surface treatment agent solution is changed.
  • the glass fillers of Examples 15 and 16 were obtained. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 13 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 5.
  • Example 18 A glass substrate was prepared in the same manner as in Example 1. The glass substrate was used as the glass filler of Comparative Example 18 without surface treatment on the glass substrate, that is, without forming a coating film. A resin composition was prepared in the same manner as in Example 13 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 5.
  • Comparative Example 19 The glass filler of Comparative Example 19 was prepared in the same manner as in Example 13 except that the concentration of the surface treatment agent in the surface treatment agent solution was changed. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 13 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 5.
  • Comparative Example 20 A glass filler of Comparative Example 20 was obtained in the same manner as in Example 13 except that the glass substrate of Example 13 was changed to a flake-shaped glass substrate (average particle size: 160 ⁇ m, average thickness: 5 ⁇ m). Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 13 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 5.
  • Comparative Example 21 The glass filler of Comparative Example 21 was obtained in the same manner as in Example 1 except that the glass substrate of Example 13 was changed to a flake-shaped glass substrate (average particle size: 160 ⁇ m, average thickness: 0.7 ⁇ m). .. Then, the content ratio of the coating film in the glass filler was measured by the same method as in Example 1. Further, a resin composition was prepared in the same manner as in Example 1 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 5.
  • Comparative Example 22 Using the E glass having the composition shown in Table 1 used for producing the glass substrate of Example 1, a circular cross-section glass fiber having a diameter of 11 ⁇ m was produced by a known spinning method. This glass fiber was pulverized with a ball mill to prepare a glass base material of Comparative Example 22 in which the number average length of the length L3 of the glass base material was 75 ⁇ m. In Comparative Example 22, the glass substrate was used as the glass filler of Comparative Example 22 without surface treatment on the glass substrate, that is, without forming a coating film. A resin composition was prepared in the same manner as in Example 13 to obtain a resin molded product. Various characteristics of the resin molded product were measured by the same method as in Example 1. The results are shown in Table 5.
  • the resin molded products produced by using the glass fillers of Examples 13 to 16 have a larger amount of warpage and inferior in dimensional stability than the resin molded products of Comparative Examples 20 and 21 using the flake-shaped glass base material, but are compared. It showed very high tensile strength and high impact strength as compared with the resin molded product of Example 20, and showed almost the same tensile strength as Comparative Example 21 and much higher impact strength than Comparative Example 21. As described above, as compared with the glass fillers of Comparative Examples 18 to 22, the glass fillers of Examples 13 to 16 have high mechanical strength and excellent dimensional stability in the molded product of the resin when blended with the resin. I was able to impart both sex.
  • the molded product of the resin composition containing the glass filler of the present invention is suitably used in the fields of interior and exterior of electrical and electronic parts where dimensional stability is required and strength is also required. More specifically, it can be applied to electrical and electronic devices and automobile materials.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
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  • General Chemical & Material Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Wood Science & Technology (AREA)
  • Composite Materials (AREA)
  • Glass Compositions (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Surface Treatment Of Glass Fibres Or Filaments (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
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EP20863173.9A EP4029842A1 (en) 2019-09-13 2020-09-01 Glass filler and resin composition
JP2021545236A JP7377275B2 (ja) 2019-09-13 2020-09-01 ガラスフィラー及び樹脂組成物
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JP2018035354A (ja) * 2016-08-29 2018-03-08 東レ株式会社 ポリフェニレンスルフィド樹脂組成物、それからなる成形品。
WO2017171101A1 (ja) * 2016-12-26 2017-10-05 日東紡績株式会社 ガラス繊維強化樹脂成形品
JP2018104529A (ja) * 2016-12-26 2018-07-05 東レ株式会社 ポリブチレンテレフタレート樹脂組成物およびそれからなる成形品
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WO2019049526A1 (ja) * 2017-09-08 2019-03-14 日東紡績株式会社 ガラス繊維用ガラス組成物、ガラス繊維及びそれを用いるガラス繊維強化樹脂組成物
WO2019074038A1 (ja) * 2017-10-13 2019-04-18 東洋紡株式会社 耐候性に優れたポリアミド樹脂組成物

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EP4029842A1 (en) 2022-07-20

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