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WO2009154062A1 - Verre sous forme de paillettes et verre sous forme de paillettes couvert - Google Patents

Verre sous forme de paillettes et verre sous forme de paillettes couvert Download PDF

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Publication number
WO2009154062A1
WO2009154062A1 PCT/JP2009/059764 JP2009059764W WO2009154062A1 WO 2009154062 A1 WO2009154062 A1 WO 2009154062A1 JP 2009059764 W JP2009059764 W JP 2009059764W WO 2009154062 A1 WO2009154062 A1 WO 2009154062A1
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WO
WIPO (PCT)
Prior art keywords
glass
mass
temperature
oxide
sio
Prior art date
Application number
PCT/JP2009/059764
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English (en)
Japanese (ja)
Inventor
浩輔 藤原
昭浩 小山
Original Assignee
日本板硝子株式会社
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Filing date
Publication date
Application filed by 日本板硝子株式会社 filed Critical 日本板硝子株式会社
Priority to JP2010517829A priority Critical patent/JP5399385B2/ja
Publication of WO2009154062A1 publication Critical patent/WO2009154062A1/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02—Preparations containing skin colorants, e.g. pigments
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/25—Silicon; Compounds thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/26—Aluminium; Compounds thereof
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B37/00—Manufacture or treatment of flakes, fibres, or filaments from softened glass, minerals, or slags
    • C03B37/005—Manufacture of flakes
    • 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
    • C03C12/00—Powdered glass; Bead compositions
    • 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
    • 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
    • C03C3/093—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium containing zinc or zirconium
    • 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
    • C09C1/0015—Pigments exhibiting interference colours, e.g. transparent platelets of appropriate thinness or flaky substrates, e.g. mica, bearing appropriate thin transparent coatings
    • C09C1/0018—Pigments exhibiting interference colours, e.g. transparent platelets of appropriate thinness or flaky substrates, e.g. mica, bearing appropriate thin transparent coatings uncoated and unlayered plate-like particles

Definitions

  • the present invention relates to scaly glass and coated scaly glass that can be used by blending, for example, in resin compositions, paints, inks (inks), cosmetics, etc., and exhibiting excellent color tone and gloss.
  • the strength and dimensional accuracy of the resin molded body obtained from the resin composition can be improved.
  • scale-like glass is mix
  • This scaly glass comes to exhibit a metallic color when its surface is coated with a metal, and the scaly glass exhibits an interference color due to interference of reflected light by coating the surface of the scaly glass with a metal oxide. It becomes like this. That is, the glass flakes coated with a metal film or metal oxide film are suitably used as a luster pigment. Bright pigments using such glass flakes are preferably used in applications where color tone and gloss are important, such as paints and cosmetics.
  • the glass flakes are produced by, for example, inflating a molten glass substrate into a balloon shape with a blow nozzle to form a hollow glass film, and pulverizing the hollow glass film with a pressure roller.
  • the glass flakes have excellent meltability and good moldability, have an appropriate temperature-viscosity characteristic, and have a devitrification temperature lower than the working temperature. Desired.
  • the working temperature is a temperature at which the viscosity of the glass is 100 Pa ⁇ s (1000 P).
  • the devitrification temperature is a temperature at which crystals start to grow in the molten glass substrate and begin to grow.
  • the working temperature is 1300 ° C. or lower because the glass flakes are difficult to be formed particularly when the working temperature is too high.
  • the thermal damage which the manufacturing apparatus of a melting kiln or scale-like glass receives becomes small, the lifetime of a melting kiln or a manufacturing apparatus can be extended.
  • the glass flakes may be subjected to a high temperature treatment.
  • the glass flakes or the coated glass flakes are blended in a paint, and may be used for applications such as baking painting and subjected to high temperature treatment. Therefore, sufficient heat resistance is also required for the glass flakes.
  • a soda lime glass generally used as a so-called plate glass composition contains a large amount of an alkali metal oxide and has insufficient heat resistance.
  • the coating film and coating film require acid resistance, alkali resistance, etc., and scaly glass requires high chemical durability.
  • the present applicant has already proposed the following glass flakes.
  • the content of silicon dioxide (SiO 2 ), the total content of silicon dioxide and aluminum oxide (Al 2 O 3 ), the total content of magnesium oxide (MgO) and calcium oxide (CaO) and it proposed the identified glass flakes a total content of sodium oxide and lithium oxide (Li 2 O) and (Na 2 O) and potassium oxide (K 2 O).
  • Patent Document 2 a scaly shape specifying the content of silicon dioxide, the total content of magnesium oxide and calcium oxide, the total content of lithium oxide, sodium oxide and potassium oxide, and the content of titanium dioxide (TiO 2 ). Suggested glass.
  • silicon dioxide and aluminum oxide are components that form a glass skeleton. If the content of silicon dioxide and aluminum oxide is not sufficiently high, the glass transition temperature does not increase, heat resistance is insufficient, water resistance, etc. Deteriorates chemical durability.
  • Diboron trioxide (B 2 O 3 ) is a component that forms a glass skeleton, adjusts the devitrification temperature and viscosity of the glass, and improves water resistance. Since silicon dioxide tends to improve acid resistance and diboron trioxide and aluminum oxide tend to deteriorate acid resistance, the balance of silicon dioxide, diboron trioxide and aluminum oxide is important.
  • Magnesium oxide and calcium oxide are components that adjust the devitrification temperature and viscosity of the glass.
  • alkali metal oxides such as lithium oxide, sodium oxide, and potassium oxide, are components which adjust the devitrification temperature and viscosity at the time of glass formation.
  • Patent Documents 1 and 2 describe that the content of aluminum oxide is preferably 5% or less.
  • the content of aluminum oxide is 3.20% by mass or less in Patent Document 1.
  • Patent Document 2 it is 4.84% by mass or less.
  • the content of silicon dioxide is set excessively compared with the content of aluminum oxide.
  • the total content of lithium oxide, sodium oxide, and potassium oxide is set to exceed 13% by mass. For this reason, there existed a problem that while the heat resistance of scale-like glass was insufficient, chemical durability, such as alkali resistance, also deteriorated.
  • the glass flakes described in Patent Documents 1 and 2 have the disadvantage that the glass transition temperature is low and the heat resistance is insufficient. Specifically, the glass transition temperatures were as low as 529 to 578 ° C. in Patent Document 1 and 467 to 576 ° C. in Patent Document 2, and sufficient heat resistance could not be expressed.
  • An object of the present invention is to provide glass flakes and coated glass flakes having improved heat resistance and chemical durability.
  • the present inventors have intensively studied on a suitable glass composition of scaly glass.
  • silicon dioxide (SiO 2 ), diboron trioxide (B 2 O 3 ) and aluminum oxide (Al 2 O 3 ) content silicon dioxide, diboron trioxide and aluminum oxide content difference (SiO 2 —B 2 O 3 —Al 2 O 3 ), by controlling the total content of alkali metal oxides (Li 2 O + Na 2 O + K 2 O), heat resistance and chemical durability (particularly acid resistance)
  • the present invention has been completed by finding that scaly glass having improved properties and easiness to mold can be obtained.
  • the scaly glass according to the first aspect of the present invention is expressed in mass%, 57 ⁇ SiO 2 ⁇ 65, 0.1 ⁇ B 2 O 3 ⁇ 2, 8 ⁇ Al 2 O 3 ⁇ 15, 45 ⁇ (SiO 2 —B 2 O 3 —Al 2 O 3 ) ⁇ 56, 1 ⁇ MgO ⁇ 5, 15 ⁇ CaO ⁇ 30, 0.1 ⁇ (Li 2 O + Na 2 O + K 2 O) ⁇ 4 It is formed from a glass substrate having a composition of
  • the glass substrate further contains 0.1 to 5% by mass of TiO 2 .
  • the glass substrate has a glass transition temperature of 600 to 800 ° C.
  • the temperature difference ⁇ T obtained by subtracting the devitrification temperature from the working temperature of the glass substrate is 0 to 100 ° C.
  • the coated flaky glass according to one aspect of the present invention includes the flaky glass according to the first aspect and a film mainly composed of a metal or a metal oxide that covers the surface of the flaky glass.
  • the glass substrate forming the glass flakes according to the first aspect of the present invention is set so as to satisfy 57 ⁇ SiO 2 ⁇ 65 and 8 ⁇ Al 2 O 3 ⁇ 15. That is, the content of silicon dioxide and aluminum oxide is sufficiently ensured, the function of forming a glass skeleton by silicon dioxide and aluminum oxide can be fully expressed, the glass transition temperature is high, the meltability is good, the acid resistance is high. Property and water resistance can be improved.
  • the content of diboron trioxide is set to 0.1 ⁇ B 2 O 3 ⁇ 2, and the difference between the content of silicon dioxide and the total content of diboron trioxide and aluminum oxide is 45 ⁇ ( SiO 2 —B 2 O 3 —Al 2 O 3 ) ⁇ 56.
  • the contents of magnesium oxide and calcium oxide are set to 1 ⁇ MgO ⁇ 5 and 15 ⁇ CaO ⁇ 30. For this reason, the devitrification temperature and viscosity at the time of glass formation can be made favorable.
  • the total content of lithium oxide, sodium oxide and potassium oxide is set to satisfy 0.1 ⁇ (Li 2 O + Na 2 O + K 2 O) ⁇ 4.
  • the content of the alkali metal oxide is sufficient, and the devitrification temperature and viscosity at the time of glass formation can be improved. Therefore, the heat resistance and chemical durability of the glass flakes can be improved.
  • the glass substrate further contains 0.1 to 5% by mass of TiO 2 , the melting property, chemical durability and ultraviolet absorption of the glass flakes can be improved due to the properties of titanium dioxide.
  • the heat resistance of the glass flakes can be improved.
  • the temperature difference ⁇ T obtained by subtracting the devitrification temperature from the working temperature of the glass substrate is set to 0 to 100 ° C., devitrification at the time of glass formation can be suppressed, and a more uniform scaly glass can be obtained. Can do.
  • coated glass flakes in which the surface of the glass flakes is coated with a film containing a metal or metal oxide as a main component can develop a metal color, an interference color or the like by the film.
  • (A) is a perspective view which shows typically the scale-like glass in embodiment
  • (b) is a top view which shows scale-like glass.
  • Sectional drawing which shows covering scale-like glass typically.
  • composition of the glass substrate that forms the scaly glass of the present embodiment is expressed as mass% and is set as follows.
  • SiO 2 is silicon dioxide (silicic acid)
  • Al 2 O 3 is aluminum oxide (alumina)
  • B 2 O 3 is diboron trioxide
  • MgO magnesium oxide
  • CaO calcium oxide
  • Li 2 O Means lithium oxide
  • Na 2 O means sodium oxide
  • K 2 O means potassium oxide.
  • FIG. 1A is a perspective view showing the scaly glass 10
  • FIG. 1B is a plan view showing the scaly glass 10.
  • the average thickness t of the glass flakes 10 of this embodiment is 0.1 to 15 ⁇ m.
  • the aspect ratio (average particle diameter a / average thickness t) of the glass flakes 10 is 2 to 1000. Therefore, the glass flakes 10 are flaky particles.
  • composition of the glass flake 10 the method for producing the glass flake 10
  • physical properties of the glass flake 10 the coated glass flakes and the uses (resin composition, paint, ink composition and cosmetic) will be described in this order.
  • composition of scale glass 10 The composition of the glass substrate forming the scale-like glass 10 will be described.
  • SiO 2 Silicon dioxide
  • the main component means a component having the largest content. Moreover, it is a component which adjusts the devitrification temperature and viscosity at the time of glass formation, and also is a component which improves acid resistance.
  • the content of SiO 2 is less than 57% by mass, the devitrification temperature is excessively increased, and it becomes difficult to form the glass flakes 10 and the acid resistance of the glass flakes 10 is also deteriorated.
  • it exceeds 65% by mass the melting point of the glass becomes too high, and it becomes difficult to uniformly melt the raw material.
  • the lower limit of SiO 2 is 57% by mass or more, preferably 58% by mass or more, more preferably 59% by mass or more, and most preferably greater than 60% by mass.
  • the upper limit of SiO 2 is 65 wt% or less, preferably 64 wt% or less. Therefore, the range of the content of SiO 2 is selected from any combination of these upper and lower limits.
  • the content of SiO 2 is preferably 57 to 64% by mass, more preferably 58 to 64% by mass.
  • Diboron trioxide (B 2 O 3 ) is a component that forms a glass skeleton, and is a component that adjusts the devitrification temperature and viscosity at the time of glass formation, and is also a component that improves water resistance.
  • the content of diboron trioxide is 0.1 ⁇ B 2 O 3 ⁇ 2.
  • B 2 O 3 which is likely to volatilize may be scattered when the glass is melted, and when the glass is melted, the furnace wall of the melting furnace or the regenerative kiln is eroded. The life of the kiln is significantly reduced.
  • the content of B 2 O 3 is less than 0.1% by mass, insufficient functional expression of B 2 O 3, with scaffolding glass it is insufficient, water resistance deteriorates.
  • the lower limit of B 2 O 3 is 0.1% by mass or more, and preferably 0.5% by mass or more.
  • the upper limit of B 2 O 3 is less than 2% by mass, and preferably 1.5% by mass or less. Therefore, any combination of these upper and lower limits is selected for the range of the content of B 2 O 3 .
  • the content of B 2 O 3 is preferably 0.1 to 1.5% by mass, and more preferably 0.5 to 1.5% by mass.
  • Aluminum oxide (Al 2 O 3 ) is a component that serves as a skeleton of the glass flake 10, and is also a component that adjusts the devitrification temperature and viscosity during glass formation.
  • Al 2 O 3 is a component that improves water resistance, while it is also a component that deteriorates acid resistance.
  • Al 2 O 3 is less than 8% by mass, the devitrification temperature and viscosity cannot be adjusted sufficiently, or the water resistance cannot be improved sufficiently.
  • the content of Al 2 O 3 exceeds 15% by mass, the melting point of the glass becomes too high, and it becomes difficult to melt the raw material uniformly, and the acid resistance is also deteriorated.
  • the lower limit of Al 2 O 3 is 8% by mass or more, and preferably 10% by mass or more.
  • the upper limit of Al 2 O 3 is 15% by mass or less, preferably 13% by mass or less, and more preferably less than 12% by mass. Therefore, the range of the content of Al 2 O 3 is selected from any combination of these upper and lower limits. For example, the content of Al 2 O 3 is preferably 10 to 15% by mass, and more preferably 10 to 13% by mass.
  • (B 2 O 3 + Al 2 O 3 ) The sum of B 2 O 3 and Al 2 O 3 (B 2 O 3 + Al 2 O 3 ), which is a component that adjusts the devitrification temperature and viscosity at the time of glass formation and improves the water resistance, is the moldability of scaly glass. Important for nirvana. When (B 2 O 3 + Al 2 O 3 ) is less than 9% by mass, the devitrification temperature rises too much, and it becomes difficult to form scale-like glass. On the other hand, if (B 2 O 3 + Al 2 O 3 ) is 17% by mass or more, the melting point of the glass becomes too high, and it becomes difficult to uniformly melt the raw material.
  • the lower limit of (B 2 O 3 + Al 2 O 3 ) is preferably 9% by mass or more, more preferably 10% by mass or more, and more preferably 11% by mass or more.
  • the upper limit of (B 2 O 3 + Al 2 O 3 ) is preferably less than 17% by mass, more preferably 16% by mass or less, further preferably 14% by mass or less, and most preferably 13% by mass or less.
  • the range of the amount of (B 2 O 3 + Al 2 O 3 ) is selected from any combination of these upper and lower limits.
  • the content of (B 2 O 3 + Al 2 O 3 ) is preferably 10 to 16% by mass, and more preferably 10 to 14% by mass.
  • SiO 2 —B 2 O 3 —Al 2 O 3 is a component for improving the acid resistance of the glass flake 10
  • the difference in the content of the B 2 O 3 and Al 2 O 3 is a component to deteriorate the acid resistance (SiO 2 -B 2 O 3 -Al 2 O 3 ) is an important factor for the acid resistance of the glass flakes 10.
  • (SiO 2 —B 2 O 3 —Al 2 O 3 ) is less than 45 mass%, the acid resistance of the glass flake 10 becomes insufficient.
  • (SiO 2 —B 2 O 3 —Al 2 O 3 ) exceeds 56 mass%, the devitrification temperature rises too much and it is difficult to form the glass flakes 10.
  • the lower limit of (SiO 2 —B 2 O 3 —Al 2 O 3 ) is 45 mass% or more, preferably 47 mass% or more, more preferably 48 mass% or more, and most preferably 49 mass% or more.
  • the upper limit of (SiO 2 —B 2 O 3 —Al 2 O 3 ) is 56 mass% or less, preferably 55 mass% or less, more preferably 54 mass% or less, and most preferably 53 mass% or less.
  • the range of the amount of (SiO 2 —B 2 O 3 —Al 2 O 3 ) is selected from any combination of these upper and lower limits.
  • the content of (SiO 2 —B 2 O 3 —Al 2 O 3 ) is preferably 45 to 55% by mass, and more preferably 46 to 53% by mass.
  • MgO, CaO Magnesium oxide (MgO) and calcium oxide (CaO) are components that adjust the devitrification temperature and viscosity during glass formation.
  • MgO Magnesium oxide
  • CaO calcium oxide
  • the lower limit of MgO is 1% by mass or more, and preferably 2% by mass or more.
  • the upper limit of MgO is 5% by mass or less, and preferably 4% by mass or less. Therefore, the content range of MgO is selected from any combination of these upper and lower limits.
  • the content of MgO is preferably 1 to 4% by mass, and more preferably 2 to 4% by mass.
  • the lower limit of CaO is 15% by mass or more, preferably 16% by mass or more, and more preferably 18% by mass or more.
  • the upper limit of CaO is 30% by mass or less, preferably 25% by mass or less, and more preferably 24% by mass or less. Therefore, the content range of CaO is determined by any combination of these upper and lower limits.
  • the CaO content is preferably 16 to 25% by mass, and more preferably 18 to 24% by mass.
  • SrO Strontium oxide
  • SrO Strontium oxide
  • the upper limit of SrO is preferably 10% by mass or less, more preferably 5% by mass or less, and further preferably 2% by mass or less. Most preferably, SrO is not substantially contained.
  • BaO Barium oxide
  • BaO is a component that adjusts the devitrification temperature and viscosity during glass formation. This BaO is not an essential component, but may be used as a component for adjusting the devitrification temperature and viscosity during glass formation. BaO is also a component that deteriorates acid resistance. However, when the content of BaO exceeds 10% by mass, the acid resistance deteriorates. Therefore, the upper limit of BaO is preferably 10% by mass or less, more preferably 5% by mass or less, and further preferably 2% by mass or less. Most preferably, BaO is not substantially contained.
  • Zinc oxide (ZnO) is a component that adjusts the devitrification temperature and viscosity during glass formation. This ZnO is not an essential component, but may be used as a component for adjusting the devitrification temperature and viscosity during glass formation. However, since ZnO is volatile, it may be scattered during melting. When the content of ZnO exceeds 10% by mass, it becomes difficult to manage the content in the glass due to volatilization. Therefore, the upper limit of ZnO is preferably 10% by mass or less, more preferably 5% by mass or less, and further preferably 2% by mass or less. Most preferably, ZnO is not substantially contained.
  • Alkali metal oxides [lithium oxide (Li 2 O), sodium oxide (Na 2 O), potassium oxide (K 2 O)] are components that adjust the devitrification temperature and viscosity during glass formation.
  • the total content (Li 2 O + Na 2 O + K 2 O) of this alkali metal oxide is 0.1 ⁇ (Li 2 O + Na 2 O + K 2 O) ⁇ 4.
  • the total content of alkali metal oxides (Li 2 O + Na 2 O + K 2 O) is more than 4% by mass, the glass transition temperature is lowered and the heat resistance of the glass is deteriorated.
  • the total content of alkali metal oxides (Li 2 O + Na 2 O + K 2 O) is less than 0.1% by mass, the devitrification temperature and viscosity cannot be adjusted sufficiently.
  • the lower limit of (Li 2 O + Na 2 O + K 2 O) is 0.1% by mass or more, and preferably 0.5% by mass or more.
  • the upper limit of (Li 2 O + Na 2 O + K 2 O) is 4% by mass or less, preferably 3% by mass or less, and more preferably less than 2% by mass.
  • the range of the amount of (Li 2 O + Na 2 O + K 2 O) is selected from any combination of these upper and lower limits.
  • the content of (Li 2 O + Na 2 O + K 2 O) is preferably 0.1 to 3% by mass, and more preferably 0.5 to 3% by mass.
  • Titanium dioxide (TiO 2 ) is a component that improves the meltability of the glass, the chemical durability of the glass flake 10 and the ultraviolet absorption characteristics. Accordingly, TiO 2 is not an essential component but is preferably included as a component for adjusting the meltability of the glass and the chemical durability and optical properties of the glass flake 10. However, when the content of TiO 2 exceeds 5% by mass, the devitrification temperature of the glass is excessively increased, and it becomes difficult to form the scaly glass 10.
  • the lower limit of Ti 2 O is preferably 0% by mass or more, and more preferably 0.1% by mass or more.
  • the upper limit of the content of TiO 2 is preferably 5% by mass or less, more preferably 2% by mass or less, still more preferably 1.6% by mass or less, and most preferably less than 1% by mass. Therefore, the range of the content of TiO 2 is determined by any combination of these upper and lower limits. For example, the content of TiO 2 is preferably 0.1 to 2% by mass.
  • ZrO 2 Zirconium oxide
  • ZrO 2 Zirconium oxide
  • Such ZrO 2 is not an essential component, but may be used as a component for adjusting the devitrification temperature, viscosity, and chemical durability during glass formation.
  • the upper limit of ZrO 2 is preferably 5% by mass or less, more preferably 2% by mass or less, and further preferably 1% by mass or less. More preferably, ZrO 2 is not substantially contained.
  • iron (Fe) in glass exists in a state of Fe 2+ or Fe 3+ .
  • Fe 3+ is a component that enhances the ultraviolet absorption characteristics of the glass flake 10
  • Fe 2+ is a component that enhances the heat ray absorption characteristics. Therefore, iron (Fe) is not an essential component, but may be included as a component for adjusting the optical properties of the glass flake 10. Moreover, even if iron (Fe) is not intentionally included, it may be inevitably mixed with industrial raw materials. On the other hand, when the content of iron (Fe) increases, the scaly glass 10 is markedly colored. This coloring may not be preferable in applications where the color tone and gloss of the glass flake 10 are regarded as important.
  • the upper limit of iron (Fe) is preferably 5% by mass or less, more preferably 2% by mass or less, further preferably 0.5% by mass or less, and particularly preferably 0.1% by mass or less in terms of Fe 2 O 3.
  • Sulfur trioxide (SO 3 ) is not an essential component, but may be included as a fining agent. When a sulfate raw material is used, it may be contained at a content of 0.5% by mass or less.
  • fluorine (F) may erode the furnace wall of a melting kiln or a heat storage kiln when melting glass, the lifetime of the kiln may be significantly reduced.
  • substantially not containing a substance means that the substance is not intentionally included unless, for example, it is inevitably mixed with an industrial raw material.
  • the content is preferably less than 0.1% by mass, more preferably 0.05% by mass or less, and particularly preferably 0.03% by mass or less.
  • the composition of the glass substrate forming the glass flakes 10 in the present embodiment includes SiO 2 , B 2 O 3 , Al 2 O 3 , MgO and CaO as essential components, and further Li 2 O. , Na 2 O and K 2 O, and containing at least one selected from the group consisting of SrO, BaO, ZnO, TiO 2 , ZrO 2 , iron oxide (FeO or Fe 2 O 3 ), SO 3 etc. may be contained.
  • the scale-like glass 10 of this embodiment can be manufactured, for example using the manufacturing apparatus shown in FIG. As shown in FIG. 4, the glass substrate 21 having the glass composition melted in the refractory kiln 20 is swelled into a balloon shape by the gas 23 sent to the blow nozzle 22 to become a hollow glass film 24. . By pulverizing the obtained hollow glass film 24 with a pair of pressing rolls 25, 25, the scaly glass 10 is obtained.
  • the scale-like glass 10 of this embodiment can be manufactured also using the manufacturing apparatus shown, for example in FIG.
  • the glass substrate 21 having the molten glass composition poured into the rotating cup 26 flows out radially from the upper edge of the rotating cup 26 by centrifugal force, and is annularly arranged vertically. The air is sucked through the gap between the plates 27 and 27 and introduced into the annular cyclone collector 28. While passing through the gap between the annular plates 27, 27, the glass substrate 21 is cooled and solidified in the form of a thin film, and further crushed into small pieces, whereby the glass flake 10 is obtained.
  • the temperature when the viscosity of the molten glass is 100 Pa ⁇ s (1000 P) is called the working temperature and is the most suitable temperature for forming the glass flake 10.
  • the working temperature is 100 Pa ⁇ s (1000 P)
  • the average thickness of the hollow glass film 24, that is, the average thickness of the scaly glass 10 is 0.1 to 15 ⁇ m.
  • the temperature drop of the glass is remarkable. Due to this temperature decrease, the plasticity of the hollow glass film 24 is drastically decreased, making it difficult to stretch.
  • the working temperature is preferably 1100 ° C. or higher, more preferably 1150 ° C. or higher, and further preferably 1200 ° C. or higher.
  • the working temperature is preferably 1260 ° C. or less, more preferably 1250 ° C. or less, further preferably 1240 ° C. or less, and most preferably 1230 ° C. or less. Therefore, the working temperature is preferably 1100 to 1300 ° C, more preferably 1200 to 1250 ° C.
  • ⁇ T is preferably 0 ° C. or higher, more preferably 20 ° C. or higher, further preferably 30 ° C. or higher, and most preferably 40 ° C. or higher.
  • ⁇ T is 100 ° C.
  • ⁇ T is more preferably 80 ° C. or lower because the glass composition can be easily adjusted, and ⁇ T is more preferably 80 ° C. or lower. Therefore, ⁇ T is preferably 0 to 100 ° C., more preferably 20 to 80 ° C., and particularly preferably 40 to 80 ° C.
  • devitrification refers to generation of white turbidity due to crystals produced and grown in a molten glass substrate.
  • a crystallized lump may exist, which is not preferable as the scale-like glass 10.
  • the scale-like glass 10 has higher heat resistance as the glass transition temperature (glass transition point) of the glass substrate forming the scale-like glass 10 is higher, and is less likely to be deformed with respect to processing involving high-temperature heating. If the glass transition temperature is 600 ° C. or higher, there is little possibility that the shape of the scaly glass 10 changes in the step of forming a film mainly composed of a metal or a metal oxide on the surface of the scaly glass 10. Moreover, the glass flakes 10 or the coated glass flakes can be blended in a paint and suitably used for applications such as baking painting. If it is a glass composition prescribed
  • the glass transition temperature of the glass flakes 10 is preferably 600 ° C. or higher, more preferably 650 ° C. or higher, and further preferably 700 ° C. or higher.
  • the upper limit of the glass transition temperature is preferably about 800 ° C. Accordingly, the glass transition temperature is preferably 600 to 800 ° C., and more preferably 650 to 800 ° C.
  • the scale-like glass 10 has a higher elasticity as the Young's modulus of the glass substrate forming the scale-like glass 10 is higher, and effectively functions as a filler for a resin composition for obtaining a resin molded body.
  • the Young's modulus (GPa) is obtained from the density of the glass measured by the Archimedes method by measuring the longitudinal wave velocity and the transverse wave velocity of the elastic wave propagating in the glass by a normal ultrasonic method. it can.
  • the lower limit of this Young's modulus is preferably 85 GPa or more, more preferably 88 GPa or more, and even more preferably 89 GPa or more.
  • the upper limit of the Young's modulus is preferably 100 GPa or less, more preferably 95 GPa or less. Therefore, the Young's modulus is preferably 85 to 100 GPa, more preferably 88 to 95 GPa.
  • the glass flake 10 of this embodiment is excellent in chemical durability such as acid resistance, water resistance, and alkali resistance. Therefore, the scale-like glass 10 of this embodiment can be used suitably for uses, such as a resin molding, a coating material, cosmetics, and ink.
  • the acid resistance index is such that the glass substrate forming the glass flake 10 is crushed and passes through the auxiliary mesh sieve 710 ⁇ m and the standard mesh sieve 590 ⁇ m specified in JIS Z 8801, but not through the standard mesh sieve 420 ⁇ m.
  • the weight reduction rate ⁇ W when glass powder is taken in the same gram quantity as the specific gravity of glass and immersed in 100 mL of an aqueous 10 mass% sulfuric acid solution at 80 ° C. for 72 hours is used. It shows that acid resistance is so high that this mass reduction rate (DELTA) W is low.
  • This measuring method is based on “Optical Glass Chemical Durability Measuring Method (Powder Method) 06-1975” of Japan Optical Glass Industry Association Standard (JOGIS).
  • the glass substrate forming the scale-like glass 10 is a glass sample produced by melting a normal glass raw material.
  • the index (mass reduction rate ⁇ W) indicating the acid resistance of the glass be a small value.
  • the weight reduction rate ⁇ W shows a large value, the anticorrosion property of the anticorrosion lining material in an acidic environment is lowered. Therefore, the weight reduction rate ⁇ W is preferably 1.2% by mass or less, more preferably 0.9% by mass or less, further preferably 0.7% by mass or less, and 0.5% by mass. % Is most preferred.
  • the lower limit of the mass reduction rate ⁇ W is usually about 0.05% by mass. Therefore, the mass reduction rate ⁇ W is preferably 0.05 to 1.2% by mass, and more preferably 0.05 to 0.9% by mass.
  • the above-described scaly glass 10 is used as a base material, and a coating 11 containing a metal or a metal oxide as a main component is formed on the surface (outer peripheral surface) thereof, thereby covering the scaly glass. 12 can be manufactured.
  • the coating 11 is preferably formed substantially from at least one of a metal and a metal oxide.
  • the form of the film 11 may be any of a single layer, a mixed layer, or a multilayer.
  • the coating 11 is formed of at least one metal selected from the group consisting of silver, gold, platinum, palladium, and nickel.
  • the coating 11 is formed of at least one metal oxide selected from the group consisting of titanium oxide, aluminum oxide, iron oxide, cobalt oxide, zirconium oxide, zinc oxide, tin oxide, and silicon dioxide.
  • titanium dioxide having high refractive index and transparency and good interference color development and iron oxide capable of developing characteristic interference colors are preferable.
  • the film 11 may be a laminated film including a first film mainly containing metal and a second film mainly containing metal oxide.
  • the film 11 may be formed on the entire surface of the glass flake 10 serving as the core, or the film 11 may be formed on a part of the surface of the glass flake 10.
  • the thickness of the coating 11 can be appropriately set depending on the application.
  • a method for forming the coating 11 on the surface of the glass flake 10 any method such as a generally known method can be employed.
  • a known method such as a sputtering method, a sol-gel method, a CVD method (chemical vapor deposition method), an LPD method, or a liquid phase deposition method in which an oxide is deposited on the surface from a metal salt can be employed.
  • the LPD method Liquid Phase Deposition Method
  • FIG. 3 is a schematic cross-sectional view for explaining an example in which the glass flake 10 is blended with a paint and applied to the surface of the substrate 13. As shown in FIG. 3, the glass flakes 10 or the coated glass flakes 12 are dispersed in the resin matrix 15 of the coating film 14.
  • Resin compositions, paints, ink compositions and cosmetics can be appropriately selected and used depending on the application as long as they are generally known.
  • the mixing ratio of the scaly glass 10 and these materials can also be set as appropriate.
  • the method of mixing the scaly glass 10 and these materials can be applied as long as it is a generally known method. For example, when the glass flakes 10 or the coated glass flakes 12 are blended in the paint, a thermosetting resin, a thermoplastic resin, or a curing agent can be appropriately selected and blended with the base material resin.
  • thermosetting resin is not particularly limited, and is an acrylic resin, polyester resin, epoxy resin, phenol resin, urea resin, fluorine resin, polyester-urethane curing resin, epoxy-polyester curing resin, acrylic-polyester resin, acrylic -Urethane curable resin, acrylic-melamine curable resin, polyester-melamine curable resin, and the like.
  • thermoplastic resin is not particularly limited, for example, polyvinyl chloride, polypropylene, polyethylene, polystyrene, polyester, polyamide, polycarbonate, polybutylene, polybutylene terephthalate or a copolymer obtained by copolymerizing monomers forming these, Examples thereof include polyphenylene sulfide, polyphenylene ether, polyether ether ketone, liquid crystal polymer (I type, II type or III type), thermoplastic fluororesin and the like.
  • the curing agent is not particularly limited, and examples thereof include polyisocyanate, amine, polyamide, polybasic acid, acid anhydride, polysulfide, trifluoroboric acid, acid dihydrazide, and imidazole.
  • the above-mentioned various thermosetting resins or thermoplastic resins can be used as a base material resin.
  • the ink composition include writing instrument inks such as various ballpoint pens and felt pens, and printing inks such as gravure inks and offset inks, and can be applied to any ink composition.
  • the vehicle constituting the ink composition serves to disperse the pigment and fix the ink to the paper.
  • the vehicle is composed of resins, oil and solvent.
  • Vehicles for writing instrument inks include acrylic resins, styrene-acrylic copolymers, polyvinyl alcohol, polyacrylic acid salts, acrylic monomer-vinyl acetate copolymers, polysaccharides produced by microorganisms such as xanthan gum, and guar gum. Examples include water-soluble plant polysaccharides. Further, examples of the solvent include water, alcohol, hydrocarbon, ester and the like.
  • Vehicles for gravure inks are resins such as gum rosin, wood rosin, tall oil rosin, lime rosin, rosin sell, maleic acid resin, polyamide resin, vinyl resin, nitrocellulose, cellulose acetate, ethyl cellulose, chlorinated rubber, cyclized rubber, ethylene-acetic acid
  • resins such as gum rosin, wood rosin, tall oil rosin, lime rosin, rosin sell, maleic acid resin, polyamide resin, vinyl resin, nitrocellulose, cellulose acetate, ethyl cellulose, chlorinated rubber, cyclized rubber, ethylene-acetic acid
  • examples thereof include a vinyl copolymer resin, a urethane resin, a polyester resin, an alkyd resin, a mixture of resins such as gilsonite, dammar, and shellac, and a water-soluble resin or an aqueous emulsion resin obtained by water-solubilizing the resin.
  • the solvent include hydrocarbon
  • the vehicle for offset ink includes rosin-modified phenolic resin, petroleum resin, alkyd resin, or these dry-modified resins as the resin, and examples of the oil include vegetable oils such as linseed oil, tung oil, and soybean oil. Further, examples of the solvent include n-paraffin, isoparaffin, aromatech, naphthene, ⁇ -olefin, water and the like. Conventional additives such as dyes, pigments, surfactants, lubricants, antifoaming agents, and leveling agents may be appropriately selected and blended with the various vehicle components described above.
  • Cosmetics include a wide range of cosmetics such as facial cosmetics, makeup cosmetics, and hair cosmetics. Among these, it is suitably applied to makeup cosmetics such as foundations, white powder, eye shadows, blushers, makeup bases, nail enamels, eye liners, mascaras, lipsticks, and fancy powders.
  • the glass flake 10 can be appropriately subjected to a hydrophobic treatment.
  • the following five methods can be mentioned as the method of hydrophobizing treatment.
  • Nylon polymethyl methacrylate, polyethylene, various fluororesins [polytetrafluoroethylene resin (PTFE), tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer resin (PFA), tetrafluoroethylene-hexafluoropropylene copolymer resin ( FEP), tetrafluoroethylene-ethylene copolymer resin (ETFE), polyvinylidene fluoride (PVDF), polychlorotrifluoroethylene (PCTFE), etc.], a treatment method with a polymer compound such as polyamino acid.
  • PTFE polytetrafluoroethylene resin
  • PFA tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer resin
  • FEP tetrafluoroethylene-hexafluoropropylene copolymer resin
  • ETFE tetrafluoroethylene-ethylene copolymer resin
  • PVDF polyvinylidene
  • any method other than those described above can be used as long as it is generally applicable to powder hydrophobization treatment.
  • other materials usually used in cosmetics can be appropriately blended with the cosmetic as needed.
  • inorganic powders include talc, kaolin, sericite, muscovite, phlogopite, saucite, biotite, lithia mica, vermiculite, magnesium carbonate, calcium carbonate, diatomaceous earth, magnesium silicate, calcium silicate, aluminum silicate, Examples thereof include barium sulfate, metal tungstate, silica, hydroxyapatite, zeolite, boron nitride, and ceramic powder.
  • organic powder examples include nylon powder, polyethylene powder, polystyrene powder, benzoguanamine powder, polytetrafluoroethylene powder, epoxy resin powder, acrylic resin powder, and microcrystalline cellulose.
  • Pigments are roughly classified into inorganic pigments and organic pigments.
  • Inorganic white pigment Titanium oxide, zinc oxide, etc.
  • Inorganic red pigment Iron oxide (Bengara), iron titanate, etc.
  • Inorganic brown pigment ⁇ iron oxide, etc.
  • Inorganic yellow pigment Yellow iron oxide, ocher, etc.
  • inorganic Black pigments black iron oxide, carbon black, etc.
  • inorganic purple pigments mango violet, cobalt violet, etc.
  • inorganic green pigments cobalt titanate, etc.
  • inorganic blue pigments ultramarine blue, bitumen, etc.
  • examples of the pearl pigment include titanium oxide coated mica, titanium oxide coated bismuth oxychloride, bismuth oxychloride, titanium oxide coated talc, fish scale foil, and colored titanium oxide coated mica.
  • examples of the metal powder pigment include aluminum powder and copper powder.
  • red 201, red 202, red 204, red 205, red 220, red 226, red 228, red 405, orange 203, orange 204, yellow 205, yellow 401 and Blue 404 etc. are mentioned.
  • organic pigments obtained by rakeizing the following dyes are used as extender pigments such as talc, calcium carbonate, barium sulfate, zirconium oxide, and aluminum white. That is, as the dye, Red No. 3, Red No. 104, Red No. 106, Red No. 227, Red No. 230, Red No. 401, Red No. 505, Orange No. 205, Yellow No. 4, Yellow No. 5, Yellow No. 202, Yellow 203, green 3 and blue 1 are listed. Furthermore, examples of the pigment include natural pigments such as chlorophyll and ⁇ -carotene.
  • hydrocarbons As hydrocarbons, squalane, liquid paraffin, petrolatum, microcrystalline wax, okezolite, ceresin, myristic acid, palmitic acid, stearic acid, oleic acid, isostearic acid, cetyl alcohol, hexadecyl alcohol, oleyl alcohol, 2-ethyl Cetyl hexanoate, 2-ethylhexyl palmitate, 2-octyldodecyl myristate, neopentyl glycol di-2-ethylhexanoate, glycerol tri-2-ethylhexanoate, 2-octyldodecyl oleate, isopropyl myristate, tris
  • Examples include glycerol isostearate, tricoconut oil fatty acid glycerol, olive oil, avocado oil, beeswax, myristyl myristate, mink oil,
  • esters such as silicone oil, higher fatty acids and oils, and oily components such as higher alcohols and waxes.
  • organic solvents such as acetone, toluene, butyl acetate, and acetate, resins such as alkyd resin and urea resin, and plasticizers such as camphor and acetyltributyl citrate can be used.
  • ultraviolet absorbers, antioxidants, preservatives, surfactants, humectants, fragrances, water, alcohols, thickeners and the like can be mentioned.
  • this cosmetic is not particularly limited, and examples thereof include powder, cake, pencil, stick, ointment, liquid, emulsion, and cream. The effect exhibited by the above embodiment is described collectively below.
  • 57 ⁇ SiO 2 ⁇ 65 and 8 ⁇ Al 2 O 3 ⁇ 15 are set as the composition of the glass substrate that forms the flaky glass 10.
  • the silicon dioxide and aluminum oxide contents are sufficiently secured, and silicon dioxide and aluminum oxide, which are components that form a glass skeleton, can fully express their functions, have a high glass transition temperature, and melt It has good properties and can improve acid resistance and water resistance.
  • the content of diboron trioxide is set to 0.1 ⁇ B 2 O 3 ⁇ 2, and the difference between the content of silicon dioxide and the total content of diboron trioxide and aluminum oxide is 45 ⁇ ( SiO 2 —B 2 O 3 —Al 2 O 3 ) ⁇ 56.
  • the composition of the three components of silicon dioxide, aluminum oxide, and diboron trioxide can combine to exhibit excellent physical properties such as heat resistance, acid resistance, and water resistance of the glass flake 10.
  • the contents of magnesium oxide and calcium oxide are set to 1 ⁇ MgO ⁇ 5 and 15 ⁇ CaO ⁇ 30.
  • the devitrification temperature and viscosity at the time of glass formation can be made favorable.
  • the devitrification temperature and viscosity at the time of glass formation are adjusted favorably by the total content of lithium oxide, sodium oxide and potassium oxide being 0.1 ⁇ (Li 2 O + Na 2 O + K 2 O) ⁇ 4. Can do.
  • the heat resistance and chemical durability of the glass flake 10 can be improved.
  • By being excellent in heat resistance deformation when the glass flakes 10 are heated to a high temperature can be suppressed.
  • it is excellent in acid resistance while being able to apply the scaly glass 10 to the anticorrosion lining material in an acidic environment, for example, as a base material of the film formed by the liquid phase method using an acidic solution Useful.
  • the working temperature can be controlled to a relatively low temperature, the glass flake 10 can be easily formed.
  • the flaky glass 10 contains 0.1 to 5% by mass of TiO 2 as a composition of the glass substrate that forms the flaky glass 10, so that the flaky glass 10 has a composition based on the properties of titanium dioxide.
  • the meltability, chemical durability, and ultraviolet absorption can be improved.
  • the heat resistance of the glass flake 10 can be further improved than before.
  • the temperature difference ⁇ T obtained by subtracting the devitrification temperature from the working temperature of the glass substrate forming the glass flake 10 is 0 to 100 ° C., devitrification during glass formation can be suppressed and more uniform A scaly glass 10 can be prepared.
  • the surface of the glass flake 10 is covered with the coating 11, and the coating 11 is formed of a metal or a metal oxide, whereby a metal color, an interference color, or the like can be developed based on the coating 11. Accordingly, the coated scale-like glass 12 can be suitably used as a bright pigment.
  • the acid resistance of the glass flakes 10 can be improved when the mass reduction rate ⁇ W of the glass substrate forming the glass flakes 10 is 0.1 to 1.2% by mass. -Since the Young's modulus of the glass substrate forming the scale-like glass 10 is 85 to 100 GPa, the scale-like glass 10 can exhibit good elasticity, and is preferably used as a filler for a resin molded body. Can do.
  • Examples 1 to 27 and Comparative Examples 1 to 8 Batches of glass bodies were prepared for each of Examples and Comparative Examples by blending ordinary glass raw materials such as silica sand so as to have the compositions shown in Tables 1 to 4. Each batch was heated to 1400-1600 ° C. using an electric furnace and melted, and maintained for about 4 hours until the composition became uniform. Thereafter, the molten glass substrate was poured out on an iron plate and gradually cooled to room temperature in an electric furnace to obtain a glass sample.
  • the platinum ball pulling method is a method of measuring the relationship between the load (resistance) and the gravity and buoyancy acting on the platinum ball when the platinum ball is immersed in molten glass and pulling the platinum ball at a constant speed.
  • This is a method of measuring the viscosity by applying the Stokes law, which shows the relationship between the viscosity and the falling speed when the particles of particles settle in the fluid.
  • a glass sample is pulverized and passed through a standard mesh sieve 1.0 mm defined in JIS Z 8801.
  • a glass sample having a size not passing through a standard mesh sieve 2.8 mm is placed in a platinum boat, and a temperature gradient (900 to 1400 ° C.
  • the glass was heated for 2 hours in an electric furnace with a), and the devitrification temperature was determined from the maximum temperature of the electric furnace corresponding to the crystal appearance position.
  • the temperature behavior at a predetermined location in the electric furnace was measured in advance.
  • a glass sample was placed in the predetermined place, and the devitrification temperature was measured.
  • Tables 1 to 4 The glass compositions in Tables 1 to 4 are all values expressed in mass%.
  • ⁇ T is a temperature difference obtained by subtracting the devitrification temperature from the working temperature as described above.
  • ⁇ W is an index of acid resistance as described above.
  • the glass of Comparative Example 1 has a conventional plate glass composition, SiO 2 , B 2 O 3 , Al 2 O 3 , (SiO 2 —B 2 O 3 —Al 2 O 3 ), CaO content and alkali
  • the total content of metal oxides (Li 2 O + Na 2 O + K 2 O) is outside the scope of the present invention.
  • the glass of Comparative Example 2 is a conventional C glass, SiO 2 , B 2 O 3 , Al 2 O 3 , (SiO 2 —B 2 O 3 —Al 2 O 3 ), CaO content and alkali metal oxide.
  • the total content Li 2 O + Na 2 O + K 2 O is outside the scope of the present invention.
  • the glass of Comparative Example 3 is a conventional E glass, and the content of SiO 2 , B 2 O 3 , (SiO 2 —B 2 O 3 —Al 2 O 3 ) and MgO is outside the scope of the present invention. Show. In the glass of Comparative Example 4, the contents of SiO 2 , B 2 O 3 and (SiO 2 —B 2 O 3 —Al 2 O 3 ) are outside the scope of the present invention.
  • the Young's modulus of the glass in Examples 1 to 27 was 89 to 92 GPa. This has shown that the scale-like glass 10 functions effectively as fillers, such as a resin molding.
  • the glass transition temperature of the glass was 619 to 711 ° C. This indicates that the scaly glass 10 can exhibit excellent heat resistance.
  • the working temperature of these glasses was 1210-1230 ° C. This indicates that the temperature is suitable for producing the scaly glass 10.
  • ⁇ T (working temperature ⁇ devitrification temperature) of these glasses was 29 to 69 ° C. This is a temperature difference that does not cause devitrification in the manufacturing process of the glass flakes 10.
  • the mass reduction rate ⁇ W which is an index of acid resistance in these glasses, was 0.12 to 0.97% by mass. This indicates that the scaly glass 10 has good acid resistance.
  • the conventional plate glass composition shown in Comparative Example 1 has a small Young's modulus of 74 GPa and is inferior in elasticity. Furthermore, the glass transition temperature of this glass is as low as 553 ° C., which is inferior in heat resistance performance.
  • the conventional C glass shown in Comparative Example 2 has a small Young's modulus of 78 GPa and is inferior in elasticity. Furthermore, the glass transition temperature of this glass is as low as 549 ° C. and is inferior in heat resistance.
  • the conventional E glass shown in Comparative Example 3 has a large mass reduction rate ⁇ W of 7.40% by mass and is inferior in acid resistance.
  • the ⁇ T (working temperature ⁇ devitrification temperature) of the glass shown in Comparative Example 4 was ⁇ 9 ° C., which was considerably smaller than the ⁇ T of the glasses shown in Examples 1 to 27, and caused devitrification. Further, the ⁇ W of this glass is 5.24% by mass, which is larger than the ⁇ W of the glasses shown in Examples 1 to 27 and is inferior in acid resistance.
  • the ⁇ T of the glass shown in Comparative Example 6 was ⁇ 16 ° C., which was smaller than the ⁇ T of the glasses shown in Examples 1 to 27 and caused devitrification. Furthermore, the mass reduction rate ⁇ W of this glass is 2.85% by mass, which is larger than the mass reduction rate ⁇ W of Examples 1 to 27 and inferior in acid resistance.
  • the ⁇ T of the glass shown in Comparative Example 7 was ⁇ 59 ° C., which was smaller than the ⁇ T of the glasses shown in Examples 1 to 27 and caused devitrification. Further, the mass reduction rate ⁇ W of this glass is 1.63 mass%, which is larger than the mass reduction rates ⁇ W of Examples 1 to 27 and inferior in acid resistance.
  • the ⁇ T of the glass shown in Comparative Example 8 was ⁇ 11 ° C., which was smaller than the ⁇ T of the glasses shown in Examples 1 to 27, and caused devitrification.
  • the content of SiO 2 , B 2 O 3 , Al 2 O 3 , (SiO 2 —B 2 O 3 —Al 2 O 3 ), MgO, CaO, and alkali metal oxides The glass whose total content (Li 2 O + Na 2 O + K 2 O) is within the range of the present invention had excellent heat resistance and chemical durability (acid resistance).
  • a glass flake 10 and a coated glass flake 12 were produced using the glasses of Examples 1 to 27 and Comparative Example 8. That is, after remelting the glass of each composition with an electric furnace, it was formed into pellets while being cooled. This pellet was put into the production apparatus shown in FIG. 4 to produce a glass flake 10 having an average thickness of 0.5 to 1 ⁇ m. The average thickness of the glass flakes was measured by measuring the thickness of the glass flakes from the cross section of 100 glass flakes using an electron microscope (Keyence Corporation, Real Surface View Microscope, VE-7800). Obtained on average.
  • Examples 28 to 54 The glass flakes 10 having the compositions of Examples 1 to 27 thus prepared were pulverized to a predetermined particle size, and then the surface of the glass flakes 10 was coated with titanium dioxide by a liquid phase method.
  • This liquid phase method is a method in which titanium dioxide is deposited on the surface of the glass flake 10 from a metal salt. That is, stannous chloride dihydrate as a metal salt was dissolved in ion-exchanged water, and diluted hydrochloric acid was added to adjust the pH to 2.0 to 2.5. To this solution, the glass flakes 10 were added with stirring, and filtered after 10 minutes.
  • hexachloroplatinic acid hexahydrate was dissolved in ion-exchanged water, and the filtered glass flake 10 was added thereto while stirring, followed by filtration after 10 minutes.
  • a hydrochloric acid solution (35% by mass) was added to ion-exchanged water to obtain a hydrochloric acid acidic solution having a pH of 0.7.
  • the glass flakes 10 were added to this acidic solution while stirring, and the solution temperature was raised to 75 ° C.
  • TiCl 4 titanium tetrachloride
  • sodium hydroxide was added simultaneously so that the pH did not change
  • titanium dioxide TiO 2
  • the glass flakes 10 having the film 11 formed on the surface was filtered and dried at 180 ° C. for 2 hours.
  • the coated scaly glass 12 produced in this way was observed with an electron microscope, and it was confirmed that a titanium oxide film 11 was formed on the surface of the scaly glass 10.
  • Examples 55 to 81 The flaky glass 10 having the composition of Examples 1 to 27 was pulverized to a predetermined particle size, and then the surface of the flaky glass 10 was coated with silver by an ordinary electroless plating method. This normal electroless plating method will be described. First, the scaly glass 10 was pretreated with stannous chloride and hexachloroplatinic acid hexahydrate in the same manner as in Examples 28 to 54. Subsequently, 200 g of silver nitrate and an appropriate amount of aqueous ammonia were added to 10 L of ion-exchanged water to produce a silver solution.
  • the coated scaly glass 12 thus prepared was observed with an electron microscope, and it was confirmed that the silver coating 11 was formed on the surface of the scaly glass 10.
  • Examples 82 to 108 and Comparative Example 9 The glass flakes 10 having the compositions of Examples 1 to 27 were pulverized to a predetermined particle size, and then mixed with a polyester resin to obtain a polyester resin composition containing the glass flakes 10. This polyester resin composition had good dispersibility of the scaly glass 10 and good appearance.
  • Comparative Example 9 the flaky glass 10 having the composition of Comparative Example 8 was pulverized to a predetermined particle size and then mixed with a polyester resin, so that the flaky glass 10 of Comparative Example 8 was devitrified.
  • the appearance of the polyester resin composition was not preferable.
  • Example 109 to 135 The coated flaky glass 12 of Examples 28 to 54 was mixed with epoxy acrylate to obtain a vinyl ester paint containing the coated flaky glass 12. This vinyl ester paint had good dispersibility of the coated scale-like glass 12 and good appearance.
  • Examples 136 to 162 The coated flaky glass 12 of Examples 28 to 54 was mixed with a foundation which is a facial cosmetic, and a cosmetic containing the coated flaky glass 12 was obtained. This cosmetic was good as a cosmetic because the dispersibility of the coated scale-like glass 12 was good.
  • Examples 163 to 189 The coated flaky glass 12 of Examples 28 to 54 was mixed with an ink composition containing a predetermined amount of a colorant, a resin, and an organic solvent, and an ink composition containing the coated flaky glass 12 was obtained.
  • This ink composition had good dispersibility of the coated scale-like glass 12, and was good as an ink composition.
  • the composition of the glass substrate the range of the content of SiO 2 + B 2 O 3 or Al 2 O 3 + B 2 O 3 is specified, the range of the components forming the glass skeleton is clarified, and the glass formation
  • the devitrification temperature and viscosity can be improved.
  • the range of MgO + CaO can be prescribed
  • the cross-sectional shape in the thickness direction of the glass flake 10 may be a shape in which two main surfaces are parallel to each other, or another shape such as a shape in which the two main surfaces are inclined (tapered). It's okay.
  • a mass reduction rate ⁇ W indicating acid resistance of the glass substrate forming the scaly glass is 0.1 to 1.2% by mass. When comprised in this way, the acid resistance of scale-like glass can be improved.
  • the working temperature of the glass substrate forming the scale-like glass is 1100-1300 ° C.
  • operativity at the time of forming a scale-like glass can be improved.
  • the Young's modulus of the glass substrate forming the glass flakes is 85 to 100 GPa.
  • scale-like glass can exhibit favorable elasticity and can be used suitably as a filler of a resin molding.
  • the metal as the main component of the coated glass flake is at least one selected from the group consisting of nickel, gold, silver, platinum and palladium.
  • the metal oxide as the main component of the coated glass flake is at least one selected from the group consisting of titanium oxide, iron oxide, cobalt oxide, zirconium oxide, zinc oxide, tin oxide and silicon oxide. .
  • a paint characterized by containing the glass flakes or the coated glass flakes. When comprised in this way, a metallic color and gloss can be provided to the coating film formed from a coating material.
  • An ink composition comprising the glass flakes or the coated glass flakes.
  • a metal color and gloss can be provided to the character, figure, etc. which are formed with an ink composition.
  • a cosmetic comprising the glass flakes or the coated glass flakes.
  • the glass flakes or the coated glass flakes When comprised in this way, after applying cosmetics to a face etc., favorable color tone and glossiness can be provided.

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Abstract

La présente invention concerne un verre sous forme de paillettes (10) présentant une meilleure résistance à la chaleur et une meilleure durabilité chimique, réalisé à partir d'un matériau de base en verre d'une composition exprimée en % de poids, telle que 57 ≤ SiO2 ≤ 65, 0,1 ≤ B2O3 < 2, 8 ≤ Al2O3 ≤ 15, 45 ≤ (SiO2 - B2O3 - Al2O3) ≤ 56, 1 ≤ MgO ≤ 5, 15 ≤ CaO ≤ 30, et 0,1 ≤ (Li2O + Na2O + K2O) ≤ 4. La température de transition vitreuse du matériau de base en verre se situe dans la plage des 600°C à 800°C. La différence de température ΔT calculée en soustrayant la température de dévitrification de la température de fonctionnement du matériau de base en verre se situe de préférence dans la plage des 0°C à 100°C.
PCT/JP2009/059764 2008-06-18 2009-05-28 Verre sous forme de paillettes et verre sous forme de paillettes couvert WO2009154062A1 (fr)

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JP2017538852A (ja) * 2014-11-24 2017-12-28 エヌジーエフ ヨーロッパ リミテッドＮｇｆ Ｅｕｒｏｐｅ Ｌｉｍｉｔｅｄ 印刷物品及びフィードストック

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JPH10231142A (ja) * 1997-02-18 1998-09-02 Nippon Electric Glass Co Ltd 耐蝕性ガラス繊維
JP2000247683A (ja) * 1999-03-04 2000-09-12 Nitto Boseki Co Ltd 耐食性を有するガラス繊維
JP2003054993A (ja) * 1997-07-04 2003-02-26 Nitto Boseki Co Ltd 繊維用ガラス組成物
JP2004508265A (ja) * 2000-09-06 2004-03-18 ピーピージー　インダストリーズ　オハイオ，　インコーポレイテッド ガラスファイバー形成組成物
WO2006068255A1 (fr) * 2004-12-24 2006-06-29 Nippon Sheet Glass Company, Limited Verre ecailleux

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JPH10231142A (ja) * 1997-02-18 1998-09-02 Nippon Electric Glass Co Ltd 耐蝕性ガラス繊維
JP2003054993A (ja) * 1997-07-04 2003-02-26 Nitto Boseki Co Ltd 繊維用ガラス組成物
JP2000247683A (ja) * 1999-03-04 2000-09-12 Nitto Boseki Co Ltd 耐食性を有するガラス繊維
JP2004508265A (ja) * 2000-09-06 2004-03-18 ピーピージー　インダストリーズ　オハイオ，　インコーポレイテッド ガラスファイバー形成組成物
WO2006068255A1 (fr) * 2004-12-24 2006-06-29 Nippon Sheet Glass Company, Limited Verre ecailleux

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017538852A (ja) * 2014-11-24 2017-12-28 エヌジーエフ ヨーロッパ リミテッドＮｇｆ Ｅｕｒｏｐｅ Ｌｉｍｉｔｅｄ 印刷物品及びフィードストック

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