WO2008050500A1 - Protective plate for portable equipment display device - Google Patents
Protective plate for portable equipment display device Download PDFInfo
- Publication number
- WO2008050500A1 WO2008050500A1 PCT/JP2007/057482 JP2007057482W WO2008050500A1 WO 2008050500 A1 WO2008050500 A1 WO 2008050500A1 JP 2007057482 W JP2007057482 W JP 2007057482W WO 2008050500 A1 WO2008050500 A1 WO 2008050500A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- protective plate
- display device
- glass
- plate
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- Prior art date
Links
- 230000001681 protective effect Effects 0.000 title claims abstract description 38
- 239000005357 flat glass Substances 0.000 claims abstract description 20
- 239000000203 mixture Substances 0.000 claims abstract description 8
- 239000011521 glass Substances 0.000 claims description 22
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 2
- 229910052593 corundum Inorganic materials 0.000 abstract 2
- 229910001845 yogo sapphire Inorganic materials 0.000 abstract 2
- 230000001413 cellular effect Effects 0.000 abstract 1
- 229910052681 coesite Inorganic materials 0.000 abstract 1
- 229910052906 cristobalite Inorganic materials 0.000 abstract 1
- 229920001690 polydopamine Polymers 0.000 abstract 1
- 239000000377 silicon dioxide Substances 0.000 abstract 1
- 235000012239 silicon dioxide Nutrition 0.000 abstract 1
- 229910052682 stishovite Inorganic materials 0.000 abstract 1
- 229910052905 tridymite Inorganic materials 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 13
- 239000010408 film Substances 0.000 description 10
- 238000005342 ion exchange Methods 0.000 description 10
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 10
- 238000004031 devitrification Methods 0.000 description 6
- 235000010333 potassium nitrate Nutrition 0.000 description 5
- 239000004323 potassium nitrate Substances 0.000 description 5
- 238000005728 strengthening Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229910052787 antimony Inorganic materials 0.000 description 3
- 229910003437 indium oxide Inorganic materials 0.000 description 3
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 238000002834 transmittance Methods 0.000 description 3
- 229910018068 Li 2 O Inorganic materials 0.000 description 2
- 238000003426 chemical strengthening reaction Methods 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 239000006060 molten glass Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 238000007088 Archimedes method Methods 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000009774 resonance method Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/083—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound
- C03C3/085—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound containing an oxide of a divalent metal
- C03C3/087—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound containing an oxide of a divalent metal containing calcium oxide, e.g. common sheet or container glass
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/133308—Support structures for LCD panels, e.g. frames or bezels
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F2201/00—Constructional arrangements not provided for in groups G02F1/00 - G02F7/00
- G02F2201/50—Protective arrangements
Definitions
- the present invention relates to a protective plate for protecting a display device of a portable device from isotropic force.
- LCD liquid crystal display
- OELD organic EL display
- Patent Document 1 Japanese Patent Application Laid-Open No. 2004-299199
- Patent Document 2 Japanese Patent Laid-Open No. 2003-140558
- a protective plate that also has glass power is required to have low transparency and be less susceptible to dirt and scratches.
- the protective plate itself is becoming increasingly thin for portable devices. It is required to reduce the wall thickness.
- An object of the present invention is to provide a protective plate for a portable device display device that can sufficiently protect the display even when the wall thickness is reduced.
- the inventors of the present invention have a particularly large amount of Al 2 O (15 to 30%) in the glass composition.
- the present invention relates to the following (1) to (6).
- a protective plate for a portable device display device comprising a plate glass having a Young's modulus of 75 GPa or more.
- a protective plate for a portable device display device comprising a plate glass containing a composition of 15 to 30%.
- Sheet glass is in mass%, SiO 50-80%, ⁇ 1 ⁇ 15-30%, ⁇ 1 ⁇ + ⁇
- the protective plate for a portable device display device which also has a glass strength containing a composition of 2 2 3 2 3 gO + ZnO 15 to 30%.
- the protective plate for a portable device display device of the present invention includes a plate glass having a Young's modulus of 75 GPa or more, it is difficult to squeeze and break even if it is thin. As a result, since the display can be sufficiently protected even if the wall thickness is reduced, the mobile device itself can be made thinner.
- the Young's modulus of the plate glass is 75 GPa or more, and preferably 78 GPa or more, more preferably 80 GPa or more.
- the protective plate for a portable device display device of the present invention is preferably such that the hardness of the plate glass is 500 Hv or more, since the surface is hardly scratched, so that it does not cause breakage and the display is difficult to see. More preferably, it is 600 Hv or more, and further preferably 650 Hv or more.
- the protective plate for a mobile device display device of the present invention has a thermal expansion coefficient of 30 to 70 10 _7 7 °, preferably 35 to 60 10 _7 7 °, more preferably 40 to 30 in the range of 30 to 380 ° C. 50 X 1 0 _ . C.
- the thermal expansion coefficient is higher than 70 ⁇ 10 _7 / ° C, the glass substrate is easily damaged by thermal strain when immersed in a molten salt such as potassium nitrate. If the thermal expansion coefficient is smaller than 30 X 10 _7 Z ° C, the thermal expansion coefficient cannot be matched with the surrounding members.
- the protective plate for a portable device display device of the present invention is preferable because it is damaged when it is strengthened.
- a sheet glass having a surface compressive stress value of 700 MPa or more is preferred because of its excellent effect of preventing breakage.
- Methods for strengthening the protective plate include a method of rapidly cooling from a temperature above the strain point (physical strengthening) and an alkali metal ion (for example, Li + or Na +) contained in the protective plate with an alkali having a large ion radius.
- an alkali metal ion for example, Li + or Na +
- a method of ion exchange with metal ions for example, K +
- the method of ion exchange is preferable because it can apply a large compressive stress to break.
- the protective plate for a portable device display device of the present invention has an antireflection film formed on at least one side (particularly the outer surface side), there is less reflection and images and images on the display device are easy to see. preferable.
- the transparent conductive film when a transparent conductive film is formed on the protective plate for a portable device display device of the present invention, it is possible to shield electromagnetic waves and to prevent contamination such as dust because it is difficult to be charged.
- oxides such as tin-containing indium oxide (ITO), antimony-containing indium oxide, and fluorine-containing indium oxide, and metal thin films such as aluminum, gold, and silver can be used.
- the protective plate for portable device display device of the present invention is formed with a scattering prevention film (scattering prevention film). It is preferable that fragments are hardly scattered even if the plate glass is broken.
- the anti-scattering film is preferred because it has an excellent effect of preventing debris from being scattered on either side, even if it is formed on either side.
- the protective plate for a portable device display device of the present invention is expressed by mass%, SiO 50-80%, Al 2 O 3
- the Young's modulus is large and difficult to stagnate.
- SiO is a component that forms a skeleton of glass. If it is less than 50%, weather resistance is obtained.
- the content of 2 is 50 to 80%, preferably 50 to 75%, more preferably 55 to 75%, more preferably 60 to 70%, and still more preferably 62 to 68%.
- Al O increases the Young's modulus and facilitates ion exchange to strengthen the surface.
- the content of 2 3 is 15 to 30%, preferably 17 to 28%, more preferably 20 to 25%.
- Al 2 O, MgO, and ZnO are components that increase the Young's modulus. 15% total content of these ingredients
- the total amount of ZnO is 15 to 33%, preferably 15 to 30%.
- MgO is not an essential component, but can be added up to a content of 5%. If it exceeds 5%, devitrification occurs and it is difficult to mold immediately. A content of 4% or less is preferred 3.5
- ZnO is not an essential component, but can be added up to a content of 5%. If it exceeds 5%, devitrification tends to occur.
- the content is preferably 4% or less, and more preferably 3.5% or less.
- Li 2 O is an ion exchange component that improves meltability, increases Young's modulus
- the content is preferably 5.5% or less, and more preferably 5.2% or less.
- Na 2 O is also an ion exchange component, improving the meltability and adjusting the thermal expansion coefficient.
- the content can be added up to 5%. If the content is more than 5%, the Young's modulus may decrease, and when a transparent conductive film such as an ITO film is formed on the glass surface, the transparent conductive film is likely to deteriorate, which is not preferable.
- the content is preferably 4.5% or less. 4. More preferably, the content is 2% or less.
- Li O and Na 2 O are components strengthened by ion exchange with K +
- 0.1% or more is preferable 0.5% or more is more preferable 1% or more is more preferable. If it is less than 1%, it is not preferable because it is difficult to sufficiently strengthen even after ion exchange with K +.
- K 2 O is a component that enhances the meltability and increases the coefficient of thermal expansion.
- the content is more than 5%, the Young's modulus may decrease, which is not preferable.
- the content is preferably 4.5% or less. 4. More preferably, the content is 2% or less.
- the total amount of Li 0, Na 2 O and ⁇ ⁇ is 0-10%. The total amount of these becomes 10% or more
- the range of the total amount of 2 2 and K ⁇ is 0 to 8%, more preferably 0.1 to 8%,
- a preferred range is 0.5 to 8%, and a particularly preferred range is 1 to 7%.
- CaO, SrO, and BaO are also components that increase the meltability and easily cause force devitrification. Therefore, these components can be added up to 8% in total. 7% or less 6. It is more preferable that it is 6.5% or less.
- TiO is a component that lowers the glass viscosity at high temperatures and imparts weather resistance
- ZrO is a component that imparts weather resistance, but is easily devitrified and difficult to melt
- PO is a component that suppresses the occurrence of devitrification, and is easy to phase-separate!
- Sb 2 O, Sb 2 O, SO, Cl, F may be added up to 2% each as a clarifier.
- the total content is more preferably 0.7% or less, and even more preferably 0.5% or less.
- Table 1 shows the glass composition and properties of each sample
- Table 2 shows the amount of stagnation of each sample
- Table 3 shows the properties before and after chemical strengthening.
- Example 1 Example 2 Comparative example 1 Comparative example 2 Material Glass Glass Glass Acrylic
- Example 1 Example 2 Comparative example 1 Comparative example 2 Substrate size Deflection amount (mm) Deflection amount (mm) Manipulation amount (mm) Deflection amount (mm)
- glass raw materials were prepared so as to have the composition shown in Table 1, and then charged into a platinum crucible.
- the molten glass was obtained using an electric furnace at 1600 ° C for 5 hours.
- the molten glass was poured onto a carbon plate, and a glass plate having a thickness of 1.2 mm was produced using a roller.
- the Young's modulus was measured by a resonance method by preparing a sample of 20 X 40 X 1 mm.
- the measuring device used was a nondestructive elastic modulus measuring system (Kanebo KI-11).
- the hardness was measured 10 times using a micro hardness tester (MXT-50 manufactured by Matsuzawa Seiki Co., Ltd.), and the average was calculated.
- the average transmittance was 40 x 40 x 0.7 mm, and the transmittance at each wavelength of 400 to 700 nm was measured using a spectrophotometer (Shimadzu UV-3100PC) with a slit width of 2n. Measured in m and averaged.
- the density was measured by the well-known Archimedes method.
- the thermal expansion coefficient was measured using a dilatometer, and the average thermal expansion coefficient at 30 to 380 ° C was used.
- each sample shown in Table 2 was prepared and arranged on a frame in which each side of the sample was supported with a width of lmm.
- an ION load was measured in a direction perpendicular to the sample surface with a rod having a square cross section of 10 mm x 10 mm in the center of the sample, and the amount of displacement at the center was measured as the amount of stagnation.
- the immersed sample was placed on a smooth ring with an inner diameter of 25 mm, and a load was applied to the center of the sample using a flat indenter with a diameter of 12.5 mm until it was damaged.
- a load was applied to the center of the sample using a flat indenter with a diameter of 12.5 mm until it was damaged.
- Example 1 As is clear from Table 1, the Young's modulus of Example 1 was 81 GPa, the Young's modulus of Example 2 was 82 GPa, and Comparative Example 1 was 70 GPa.
- Example 1 and Example 2 after strengthening had higher average fracture strength than Comparative Example 1 after strengthening.
- Example 1 and Comparative Example 1 a 35 ⁇ 35 ⁇ 0.5 mm plate-like sample was immersed in molten potassium nitrate set at 500 ° C. All the end surfaces of these plate samples were polished with # 600 water-resistant abrasive paper, and both surfaces were optically polished. In addition, the time until one plate-like sample was completely immersed in potassium nitrate molten salt was within 1 second, and the number of damaged plate samples for Example 1 and Comparative Example 1 was examined. As a result, in Example 1, the number of damaged sheets was 0 out of 50 sheets, whereas in Comparative Example 1, the number of damaged sheets was 5 out of 50 sheets. there were.
- the protective plate for a portable device display device of the present invention can be used as a protective plate for displays such as portable game machines, portable music players, IC recorders, electronic dictionaries, etc., which can be used only with a mobile phone, a digital camera, or a PDA. is there.
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- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Nonlinear Science (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mathematical Physics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
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- Optics & Photonics (AREA)
- Glass Compositions (AREA)
Abstract
This invention provides a protective plate for a portable equipment display device, characterized by comprising a plate glass having a Young's modulus of not less than 75 GPa. Further, the protective plate for a portable equipment display device is characterized by comprising a plate glass having a composition comprising, by mass, 50 to 80% of SiO2, 15 to 30% of Al2O3, and 15 to 30% of Al2O3 + MgO + ZnO. The protective plate for a portable equipment display device is usable as protective plates for displays for cellular phones, digital cameras, and PDAs, as well as for displays, for example, for portable gaming machines, portable music players, IC recorders, and electronic dictionaries.
Description
明 細 書 Specification
携帯機器表示装置用保護板 Protection plate for portable device display device
技術分野 Technical field
[0001] 本発明は、携帯機器の表示装置の破損等力 保護するための保護板に関するもの である。 [0001] The present invention relates to a protective plate for protecting a display device of a portable device from isotropic force.
背景技術 Background art
[0002] 近年、携帯機器、特に携帯電話、デジタルカメラや携帯情報端末 (PDA)は、小型 ィ匕、軽量化、薄肉化が図られている。一方、それらのディスプレイは大型化が図られ て 、る。このようなディスプレイには液晶ディスプレイ (LCD)や有機 ELディスプレイ ( OELD)が主に使用されている。 In recent years, mobile devices, particularly mobile phones, digital cameras, and personal digital assistants (PDAs) have been reduced in size, weight, and thickness. On the other hand, these displays are becoming larger. Liquid crystal displays (LCD) and organic EL displays (OELD) are mainly used for such displays.
[0003] これらのディスプレイには、テレビやパソコンのモニタのように固定して使用するディ スプレイに比べて取り扱い上、衝撃や外力が加わりやすい。例えば、 LCDに外力が カロわると、「パドリング」と呼ばれる画像の乱れが生じたり、ガラス基板が破損したりす る場合がある。そのため、ディスプレイを保護するために透明な榭脂板 (保護板)がデ イスプレイと平行に一定幅の間隔を介して設置されている(例えば、特許文献 1参照。 [0003] These displays are more susceptible to impacts and external forces in handling than displays that are fixed and used, such as monitors of televisions and personal computers. For example, when external force is applied to the LCD, image disturbance called “paddling” may occur or the glass substrate may be damaged. Therefore, in order to protect the display, a transparent resin plate (protective plate) is installed in parallel with the display via a fixed width interval (see, for example, Patent Document 1).
) o ) o
[0004] しかし、榭脂板は長期間にわたって使用すると、榭脂が劣化して透明度が低下した り、表面に汚れや傷がついたりしてディスプレイが見に《なるという問題を有していた 。このような問題を解決するために榭脂板の替わりにガラス板を保護板に使用するこ とが提案されている (例えば、特許文献 2参照。 )0 [0004] However, when the resin board is used for a long period of time, the resin deteriorates and the transparency is lowered, or the surface is soiled or scratched, resulting in a problem that the display becomes visible. . That you use to protect plate glass plate has been proposed in order to solve such problem instead of榭脂plate (e.g., see Patent Document 2.) 0
特許文献 1:特開 2004- 299199号公報 Patent Document 1: Japanese Patent Application Laid-Open No. 2004-299199
特許文献 2:特開 2003- 140558号公報 Patent Document 2: Japanese Patent Laid-Open No. 2003-140558
発明の開示 Disclosure of the invention
[0005] ガラス力もなる保護板には、上記したように透明度が低下すること、汚れや傷がつき にくいことなどが要求されるが、特に近年、携帯機器の薄肉化のために保護板自体 の肉厚を薄くすることが要求されて 、る。 [0005] As described above, a protective plate that also has glass power is required to have low transparency and be less susceptible to dirt and scratches. However, in recent years, the protective plate itself is becoming increasingly thin for portable devices. It is required to reduce the wall thickness.
[0006] しかし、ガラス力 なる保護板の肉厚を薄くすると、破損しやすくなるとともに橈みや
すく保護板として機能しな 、おそれがある。 [0006] However, if the thickness of the protective plate made of glass is reduced, the protective plate tends to break and Does not function as a protective plate.
[0007] 本発明の目的は、肉厚を薄くしても充分にディスプレイを保護できる携帯機器表示 装置用保護板を提供することである。 [0007] An object of the present invention is to provide a protective plate for a portable device display device that can sufficiently protect the display even when the wall thickness is reduced.
[0008] 本発明者等は、鋭意検討した結果、ガラスの組成に特に Al Oを多く(15〜30%) [0008] As a result of intensive studies, the inventors of the present invention have a particularly large amount of Al 2 O (15 to 30%) in the glass composition.
2 3 twenty three
添加すると、ガラス板が橈みにくくなることと、化学強化による効果が高くなり破損しに くくなることを見いだし、本発明として提案するものである。 When added, it is found that the glass plate becomes difficult to squeeze, and the effect of chemical strengthening becomes high and it is difficult to break, which is proposed as the present invention.
すなわち、本発明は以下の(1)〜(6)に関する。 That is, the present invention relates to the following (1) to (6).
(1) ヤング率が 75GPa以上の板ガラスを備えてなることを特徴とする携帯機器表 示装置用保護板。 (1) A protective plate for a portable device display device, comprising a plate glass having a Young's modulus of 75 GPa or more.
(2) 板ガラスが物理強化または化学強化されていることを特徴とする(1)に記載の 携帯機器表示装置用保護板。 (2) The protective plate for a portable device display device according to (1), wherein the plate glass is physically strengthened or chemically strengthened.
(3) 板ガラスの表面圧縮応力値が 700MPa以上であることを特徴とする(1)また は (2)に記載の携帯機器表示装置用保護板。 (3) The protective plate for a portable device display device according to (1) or (2), wherein the plate glass has a surface compressive stress value of 700 MPa or more.
(4) 板ガラスの表面に飛散防止フィルムが貼付されてなることを特徴とする(1)〜( 3)の 、ずれかに記載の携帯機器表示装置用保護板。 (4) The protective plate for a portable device display device according to any one of (1) to (3), wherein a scattering prevention film is adhered to the surface of the plate glass.
(5) 質量%表示で、 SiO 50〜80%、Α1 Ο 15〜30%、 Al O +MgO+ZnO (5) By mass%, SiO 50-80%, Α1 Ο 15-30%, Al O + MgO + ZnO
2 2 3 2 3 2 2 3 2 3
15〜30%の組成を含有する板ガラスを備えてなることを特徴とする携帯機器表示 装置用保護板。 A protective plate for a portable device display device, comprising a plate glass containing a composition of 15 to 30%.
(6) 板ガラスが質量%表示で、 SiO 50〜80%、Α1 Ο 15〜30%、Α1 Ο +Μ (6) Sheet glass is in mass%, SiO 50-80%, Α1 Ο 15-30%, Α1 Ο + Μ
2 2 3 2 3 gO+ZnO 15〜30%の組成を含有するガラス力もなることを特徴とする請求項 1〜 4の 、ずれかに記載の携帯機器表示装置用保護板。 The protective plate for a portable device display device according to any one of claims 1 to 4, which also has a glass strength containing a composition of 2 2 3 2 3 gO + ZnO 15 to 30%.
[0009] 本発明の携帯機器表示装置用保護板は、ヤング率が 75GPa以上の板ガラスを備 えてなるため、肉厚が薄くても橈みにくいとともに破損しにくい。その結果、肉厚を薄く してもディスプレイを充分に保護することができるため、携帯機器自体も薄肉化するこ とがでさる。 [0009] Since the protective plate for a portable device display device of the present invention includes a plate glass having a Young's modulus of 75 GPa or more, it is difficult to squeeze and break even if it is thin. As a result, since the display can be sufficiently protected even if the wall thickness is reduced, the mobile device itself can be made thinner.
発明を実施するための最良の形態 BEST MODE FOR CARRYING OUT THE INVENTION
[0010] 以下、本発明について詳細に説明する。 なお、本明細書における百分率等は、 特に示されない限り、それぞれ質量を基準とする。また、質量で定義される全ての百
分率等は、それぞれ重量で定義されるそれらと同一である。 [0010] Hereinafter, the present invention will be described in detail. The percentages and the like in this specification are based on mass unless otherwise indicated. All hundreds defined by mass The fractions and the like are the same as those defined by weight.
[0011] 板ガラスのヤング率は、 75GPa以上であり、 78GPa以上であると好ましぐ 80GPa 以上であるとより好ましい。 [0011] The Young's modulus of the plate glass is 75 GPa or more, and preferably 78 GPa or more, more preferably 80 GPa or more.
[0012] 本発明の携帯機器表示装置用保護板は、板ガラスの硬度が 500Hv以上であると 表面に傷がつきにくいため、破損の原因にならないとともに、表示が見にくくならず好 ましい。 600Hv以上であるとより好ましく、 650Hv以上であるとさらに好ましい。 [0012] The protective plate for a portable device display device of the present invention is preferably such that the hardness of the plate glass is 500 Hv or more, since the surface is hardly scratched, so that it does not cause breakage and the display is difficult to see. More preferably, it is 600 Hv or more, and further preferably 650 Hv or more.
本発明の携帯機器表示装置用保護板は、 30〜380°Cの範囲において熱膨張係 数が30〜70 10_77°〇、好ましくは35〜60 10_77°〇、より好ましくは 40〜50 X 1 0_ン。 Cである。熱膨張係数が 70 X 10_7/°Cより高くなると、硝酸カリウム等の溶融塩 に浸漬した際、熱歪によってガラス基板が破損しやすくなる。また熱膨張係数が 30 X 10_7Z°Cより小さいと周辺部材との熱膨張係数の整合性がとれない。 The protective plate for a mobile device display device of the present invention has a thermal expansion coefficient of 30 to 70 10 _7 7 °, preferably 35 to 60 10 _7 7 °, more preferably 40 to 30 in the range of 30 to 380 ° C. 50 X 1 0 _ . C. When the thermal expansion coefficient is higher than 70 × 10 _7 / ° C, the glass substrate is easily damaged by thermal strain when immersed in a molten salt such as potassium nitrate. If the thermal expansion coefficient is smaller than 30 X 10 _7 Z ° C, the thermal expansion coefficient cannot be matched with the surrounding members.
[0013] 本発明の携帯機器表示装置用保護板は、強化されていると破損しに《なるため好 ましい。特に板ガラスの表面圧縮応力値が 700MPa以上であると、破損を防止する 効果に優れるため好まし 、。 [0013] The protective plate for a portable device display device of the present invention is preferable because it is damaged when it is strengthened. In particular, a sheet glass having a surface compressive stress value of 700 MPa or more is preferred because of its excellent effect of preventing breakage.
[0014] 保護板を強化する方法としては、歪点以上の温度から急激に冷却する方法 (物理 強化)や、保護板が含有するアルカリ金属イオン (例えば、 Li+や Na+)をイオン半径の 大きなアルカリ金属イオン (例えば、 K+)とイオン交換する方法 (ィ匕学強化)が広く使用 されているが、イオン交換する方法の方が大きな圧縮応力を付与できるため破損しに 《好ましい。 [0014] Methods for strengthening the protective plate include a method of rapidly cooling from a temperature above the strain point (physical strengthening) and an alkali metal ion (for example, Li + or Na +) contained in the protective plate with an alkali having a large ion radius. A method of ion exchange with metal ions (for example, K +) (strengthening of chemicals) is widely used. However, the method of ion exchange is preferable because it can apply a large compressive stress to break.
[0015] 本発明の携帯機器表示装置用保護板は、少なくとも片面 (特に外表面側)に反射 防止膜が形成されて!ヽると、写りこみが少なく表示装置の画像や映像が見やすくなる ため好ましい。 [0015] When the protective plate for a portable device display device of the present invention has an antireflection film formed on at least one side (particularly the outer surface side), there is less reflection and images and images on the display device are easy to see. preferable.
[0016] また、本発明の携帯機器表示装置用保護板に、透明導電膜が形成されていると、 電磁波を遮蔽できるとともに、帯電しにくいためほこりなど汚れが付着しにくい。透明 導電膜としては、スズ含有酸化インジウム (ITO)、アンチモン含有酸化インジウム、フ ッ素含有酸化インジウム等の酸化物やアルミニウム、金、銀等の金属薄膜が使用可 能である。 In addition, when a transparent conductive film is formed on the protective plate for a portable device display device of the present invention, it is possible to shield electromagnetic waves and to prevent contamination such as dust because it is difficult to be charged. As the transparent conductive film, oxides such as tin-containing indium oxide (ITO), antimony-containing indium oxide, and fluorine-containing indium oxide, and metal thin films such as aluminum, gold, and silver can be used.
[0017] 本発明の携帯機器表示装置用保護板は、飛散防止膜 (飛散防止フィルム)が形成
されていると、板ガラスが破損しても破片が飛散しにくいため好ましい。飛散防止膜 は、どちらの面に形成されて ヽても良 ヽが外表面側に形成されて ヽると破片の飛散 を防止する効果に優れるため好まし 、。 [0017] The protective plate for portable device display device of the present invention is formed with a scattering prevention film (scattering prevention film). It is preferable that fragments are hardly scattered even if the plate glass is broken. The anti-scattering film is preferred because it has an excellent effect of preventing debris from being scattered on either side, even if it is formed on either side.
[0018] 本発明の携帯機器表示装置用保護板は、質量%表示で、 SiO 50〜80%、 Al O [0018] The protective plate for a portable device display device of the present invention is expressed by mass%, SiO 50-80%, Al 2 O 3
2 2 twenty two
15〜30%、 AI O +MgO+ZnO 15〜30%の組成を含有するガラスからなるとWhen made of glass containing a composition of 15-30%, AI O + MgO + ZnO 15-30%
3 2 3 3 2 3
、ヤング率が大きく橈みにくいため好ましい。 The Young's modulus is large and difficult to stagnate.
[0019] SiOは、ガラスの骨格を形成する成分である。 50%よりも少ないと耐候性が得られ [0019] SiO is a component that forms a skeleton of glass. If it is less than 50%, weather resistance is obtained.
2 2
にくい傾向があり、 80%よりも多いとガラスの粘性が高くなるため溶融が難しくなる傾 向があるとともに、液相温度が上昇するため成形が困難になりやすい。従って、 SiO If it exceeds 80%, the viscosity of the glass tends to increase and melting tends to be difficult, and the liquidus temperature rises, making it difficult to form. Therefore, SiO
2 の含有量は、 50〜80%、好ましくは 50〜75%、より好ましくは 55〜75%であり、さら に好ましくは 60〜70%であり、よりさらに好ましくは 62〜68%である。 The content of 2 is 50 to 80%, preferably 50 to 75%, more preferably 55 to 75%, more preferably 60 to 70%, and still more preferably 62 to 68%.
[0020] Al Oは、ヤング率を高めるとともに、イオン交換を促進して強化しやすくして、表面 [0020] Al O increases the Young's modulus and facilitates ion exchange to strengthen the surface.
2 3 twenty three
圧縮応力値を大きくすることができる成分でもある。 15%よりも少ないと上記の効果を 充分に得にくい傾向があり、 30%よりも多いとガラスの粘性が高くなるため溶融が難 しくなるとともに、液相温度が上昇するため成形が困難になりやすい。従って、 Al O It is also a component that can increase the compressive stress value. If the amount is less than 15%, the above effect tends to be difficult to obtain.If the amount is more than 30%, the viscosity of the glass becomes high, so that it becomes difficult to melt, and the liquidus temperature rises to make molding difficult. Cheap. Therefore, Al O
2 3 の含有量は、 15〜30%、好ましくは 17〜28%であり、より好ましくは 20〜25%であ る。 The content of 2 3 is 15 to 30%, preferably 17 to 28%, more preferably 20 to 25%.
[0021] Al O、 MgO、 ZnOは、ヤング率を高める成分である。これらの成分の合量が 15% [0021] Al 2 O, MgO, and ZnO are components that increase the Young's modulus. 15% total content of these ingredients
2 3 twenty three
よりも少な 、とヤング率を充分に大きく出来な 、傾向があり、 33%よりも多 、と溶融し にくかったり、失透が発生しやす力つたりするため好ましくない。従って、 Al O、 Mg If the ratio is less than 33%, the Young's modulus cannot be sufficiently increased, and if it is more than 33%, it tends to be difficult to melt or devitrification is likely to occur. Therefore, Al O, Mg
2 3 twenty three
0、 ZnOの合量は、 15〜33%であり、好ましくは 15〜30%である。 0, the total amount of ZnO is 15 to 33%, preferably 15 to 30%.
[0022] MgOは、必須成分ではないが、含有量が 5%まで添加することができる。 5%よりも 多いと失透が発生しやすぐ成形しにくい。含有量は 4%以下であると好ましぐ 3. 5[0022] MgO is not an essential component, but can be added up to a content of 5%. If it exceeds 5%, devitrification occurs and it is difficult to mold immediately. A content of 4% or less is preferred 3.5
%以下であるとより好ましい。 It is more preferable that it is% or less.
[0023] ZnOも必須成分ではないが、含有量が 5%まで添加することができる。 5%よりも多 いと失透が発生しやすい。含有量は 4%以下であると好ましぐ 3. 5%以下であるとよ り好ましい。 [0023] ZnO is not an essential component, but can be added up to a content of 5%. If it exceeds 5%, devitrification tends to occur. The content is preferably 4% or less, and more preferably 3.5% or less.
[0024] 上記した以外にも以下の成分を添加することができる。
[0025] Li Oは、イオン交換成分であり、溶融性を向上させたり、ヤング率を高めたり、熱膨In addition to the above, the following components can be added. [0025] Li 2 O is an ion exchange component that improves meltability, increases Young's modulus,
2 2
張係数を調整する成分であり、 6%まで添加することができる。含有量が 6%よりも多 いとガラスが失透しやすくなつたり、分相によって白濁しやすくなつたりする。また熱膨 張係数が高くなりすぎて、イオン交換時に硝酸カリウム溶融塩等に浸漬した際ガラス が割れやすくなつたりする恐れがある。含有量は 5. 5%以下であると好ましぐ 5. 2% 以下であるとより好ましい。一方、ガラスのヤング率、イオン交換性能を向上させると いう観点から、 Li Oは 0. 1%以上含有することが好ましぐ 0. 5%以上であるとより好 It is a component that adjusts the tension coefficient and can be added up to 6%. If the content is more than 6%, the glass tends to be devitrified or it may become cloudy due to phase separation. In addition, the coefficient of thermal expansion becomes too high, and there is a risk that the glass will break easily when immersed in molten potassium nitrate during ion exchange. The content is preferably 5.5% or less, and more preferably 5.2% or less. On the other hand, from the viewpoint of improving the Young's modulus and ion exchange performance of the glass, it is preferable to contain 0.1% or more of Li 2 O, and more preferably 0.5% or more.
2 2
ましぐ 1%以上であるとさらに好ましい。 More preferably, it is 1% or more.
[0026] Na Oもイオン交換成分であり、溶融性を向上させたり、熱膨張係数を調整したりす [0026] Na 2 O is also an ion exchange component, improving the meltability and adjusting the thermal expansion coefficient.
2 2
る成分であり、 5%まで添加することができる。含有量が 5%よりも多いとヤング率が低 下するおそれがあり、ガラス表面に ITO膜等の透明導電膜を形成した場合、透明導 電膜を劣化させやすいため好ましくない。含有量は 4. 5%以下であると好ましぐ 4. 2%以下であるとより好まし 、。 It can be added up to 5%. If the content is more than 5%, the Young's modulus may decrease, and when a transparent conductive film such as an ITO film is formed on the glass surface, the transparent conductive film is likely to deteriorate, which is not preferable. The content is preferably 4.5% or less. 4. More preferably, the content is 2% or less.
[0027] Li Oと Na Oは、 K+とイオン交換することによって強化される成分であるため合量で [0027] Li O and Na 2 O are components strengthened by ion exchange with K +,
2 2 twenty two
0. 1%以上含有していることが好ましぐ 0. 5%以上であるとより好ましぐ 1%以上で あるとより好ましい。 0. 1%よりも少ないと K+とイオン交換しても充分に強化されにくい ため好ましくない。 0.1% or more is preferable 0.5% or more is more preferable 1% or more is more preferable. If it is less than 1%, it is not preferable because it is difficult to sufficiently strengthen even after ion exchange with K +.
[0028] K Oは、溶融性を高めるとともに熱膨張係数を大きくする成分であり、 5%まで添カロ [0028] K 2 O is a component that enhances the meltability and increases the coefficient of thermal expansion.
2 2
することができる。含有量が 5%よりも多いと、ヤング率が低下するおそれがあるため 好ましくない。含有量は 4. 5%以下であると好ましぐ 4. 2%以下であるとより好まし い。 can do. If the content is more than 5%, the Young's modulus may decrease, which is not preferable. The content is preferably 4.5% or less. 4. More preferably, the content is 2% or less.
Li 0、 Na O及び Κ Οの合量は 0〜10%である。これらの合量が 10%以上になる The total amount of Li 0, Na 2 O and Κ Ο is 0-10%. The total amount of these becomes 10% or more
2 2 2 2 2 2
と、ガラスの熱膨張係数が高くなりすぎてイオン交換を行う際に、熱歪によってガラス の割れが起こりやすくなり、生産性が低下する場合がある。好ましい Li 0、 Na O及 When the ion exchange is performed because the glass has a too high thermal expansion coefficient, the glass is likely to break due to thermal strain, which may reduce productivity. Preferred Li 0, Na O and
2 2 び K Οの合量の範囲は 0〜8%であり、より好ましい範囲は 0. 1〜8%であり、さらに The range of the total amount of 2 2 and K Ο is 0 to 8%, more preferably 0.1 to 8%,
2 2
好ましい範囲は、 0. 5〜8%であり、特に好ましい範囲は 1〜7%である。 A preferred range is 0.5 to 8%, and a particularly preferred range is 1 to 7%.
[0029] CaO、 SrOおよび BaOは、溶融性を高める成分である力 失透が発生しやす!/ヽ成 分でもある。そのためこれらの成分は合量で 8%まで添加することができる。 7%以下
であると好ましぐ 6. 5%以下であるとより好ましい。 [0029] CaO, SrO, and BaO are also components that increase the meltability and easily cause force devitrification. Therefore, these components can be added up to 8% in total. 7% or less 6. It is more preferable that it is 6.5% or less.
[0030] TiOは、高温でのガラス粘度を低くするとともに耐候性を付与する成分であるが、 [0030] TiO is a component that lowers the glass viscosity at high temperatures and imparts weather resistance,
2 2
失透が発生しやすい成分であり、 8%まで添加することができる。 6%以下であると好 ましぐ 4%以下であるとより好ましい。 It is a component that easily causes devitrification and can be added up to 8%. It is preferably 6% or less, more preferably 4% or less.
[0031] ZrOは、耐候性を付与する成分であるが、失透しやすいとともに溶融しにくい成分 [0031] ZrO is a component that imparts weather resistance, but is easily devitrified and difficult to melt
2 2
でもあり、 7%まで添加することができる。 5%以下であると好ましぐ 4%以下であると より好まし 、。 However, up to 7% can be added. 5% or less is preferred 4% or less is more preferred
[0032] P Oは、失透の発生を抑制する成分である力 分相しやす!/、成分であるため 7%ま [0032] PO is a component that suppresses the occurrence of devitrification, and is easy to phase-separate!
2 5 twenty five
で添加することができる。 5%以下であると好ましぐ 4%以下であるとより好ましい。 Can be added. 5% or less is preferable 4% or less is more preferable.
[0033] 清澄剤として As O、 Sb O、 Sb O、 SO、 Cl、 Fをそれぞれ 2%まで添カ卩してもよ [0033] As O, Sb 2 O, Sb 2 O, SO, Cl, F may be added up to 2% each as a clarifier.
2 3 2 3 2 5 3 2 3 2 3 2 5 3
いが、 As Oは、環境負荷物質であるため含有しないことが好ましい。 However, it is preferable not to contain As O because it is an environmentally hazardous substance.
2 3 twenty three
[0034] 有色酸化物である Fe O、 CuO、 CoO、 Cr O、 NiO等の含有量は合量で 1%以下 [0034] Content of colored oxides such as Fe 2 O, CuO, CoO, Cr 2 O, NiO, etc. is 1% or less in total
2 3 2 3 2 3 2 3
であることが好ましい。合量の含有量が 0. 7%以下であるとより好ましぐ 0. 5%以下 であるとさらに好ましい。 It is preferable that The total content is more preferably 0.7% or less, and even more preferably 0.5% or less.
実施例 Example
[0035] 以下、実施例と比較例を用いて本発明を詳細に説明する。 Hereinafter, the present invention will be described in detail using examples and comparative examples.
[0036] 表 1は各試料のガラス組成および特性を示し、表 2は各試料の橈み量を示し、表 3 は化学強化前後の特性を示す。 [0036] Table 1 shows the glass composition and properties of each sample, Table 2 shows the amount of stagnation of each sample, and Table 3 shows the properties before and after chemical strengthening.
[0037] [表 1]
[0037] [Table 1]
実施例 1 実施例 2 比較例 1 比較例 2 材質 ガラス ガラス ガラス ァク リ ノレExample 1 Example 2 Comparative example 1 Comparative example 2 Material Glass Glass Glass acrylic
S i O 2 (wt%) 66.0 65.6 67.0 S i O 2 (wt%) 66.0 65.6 67.0
A 1 2 O 3 22.0 22.0 6.0 A 1 2 O 3 22.0 22.0 6.0
L i 2 O 4.0 4.0 ― L i 2 O 4.0 4.0 ―
N a 2 O 0.5 0.4 14.0 N a 2 O 0.5 0.4 14.0
K 2 O 0.5 0.5 2.0 K 2 O 0.5 0.5 2.0
M g O ― 0.8 3.0 M g O ― 0.8 3.0
C a O ― ― 7.5 C a O ― ― 7.5
S r O ― ― ― S r O ― ― ―
B a O 0.5 0.2 ― B a O 0.5 0.2 ―
Z n O ― ― 0.5 Z n O ― ― 0.5
T i O 2 2.0 2.0 ― T i O 2 2.0 2.0 ―
Z r O 2 2.0 2.0 ― Z r O 2 2.0 2.0 ―
P 2 O 5 1.5 1.5 ― P 2 O 5 1.5 1.5-
S b a O a 1.0 1.0 ― S b a O a 1.0 1.0 ―
ヤング率 (GPa) 81 82 70 3.0 硬度 ( H v ) 700 710 640 Young's modulus (GPa) 81 82 70 3.0 Hardness (Hv) 700 710 640
平均透過率 (%) 91.4 91.0 91.5 92 密度 (g/cm3) 2.4 2.4 2.5 1.2 熱膨張係数 Average transmittance (%) 91.4 91.0 91.5 92 Density (g / cm 3 ) 2.4 2.4 2.5 1.2 Thermal expansion coefficient
44 44.5 93.6 ― 44 44.5 93.6 ―
( 1 0 一 7 /0 C )
(1 0 one 7/0 C)
実施例 1 実施例 2 比較例 1 比較例 2 基板サイズ 撓み量(mm) 撓み量 ( mm ) 操み量 (mm) 撓み量(mm)Example 1 Example 2 Comparative example 1 Comparative example 2 Substrate size Deflection amount (mm) Deflection amount (mm) Manipulation amount (mm) Deflection amount (mm)
25 x 35 x 1 . 0 m m 0. 01 0. 01 0. 01 0. 325 x 35 x 1.0 mm 0. 01 0. 01 0. 01 0. 3
50 x 70 1 . O m m 0. 05 0. 05 0. 06 1 . 350 x 70 1 .O m m 0. 05 0. 05 0. 06 1. 3
25 x 35 x 0. 7 m m 0. 03 0. 03 0. 04 0. 925 x 35 x 0.7 m m 0. 03 0. 03 0. 04 0. 9
50 x 70 x 0. 7 m m 0. 1 4 0. 1 4 0. 1 7 3. 850 x 70 x 0.7 mm 0. 1 4 0. 1 4 0. 1 7 3. 8
25 35 x 0. 4 m m 0. 1 7 0. 1 7 0. 20 未測定25 35 x 0.4 mm 0. 1 7 0. 1 7 0. 20 Not measured
50 X 70 X 0. 4 m m 0. 76 0. 75 0. 88 未測定 50 X 70 X 0.4 m m 0. 76 0. 75 0. 88 Not measured
[0039] [表 3] [0039] [Table 3]
[0040] 各試料 (実施例および比較例 1)は以下のようにして作製した。 [0040] Each sample (Example and Comparative Example 1) was produced as follows.
[0041] まず、表 1に記載の組成となるようにガラス原料を調合した後、白金ルツボに投入し [0041] First, glass raw materials were prepared so as to have the composition shown in Table 1, and then charged into a platinum crucible.
、 1600°Cで 5時間電気炉を用いて溶融ガラスとした。 The molten glass was obtained using an electric furnace at 1600 ° C for 5 hours.
[0042] 次に、溶融ガラスをカーボン板上に流し出し、ローラーを用いて 1. 2mmの厚さのガ ラス板を作製した。 [0042] Next, the molten glass was poured onto a carbon plate, and a glass plate having a thickness of 1.2 mm was produced using a roller.
[0043] 最後に、 650°Cでァニールした後、表面を光学研摩して試料とした。 [0043] Finally, after annealing at 650 ° C, the surface was optically polished to prepare a sample.
[0044] ヤング率は、 20 X 40 X 1mmの試料を作製し、共振法により測定した。測定装置は 非破壊弾性率測定システム (鐘紡製 KI-11)を用いた。 [0044] The Young's modulus was measured by a resonance method by preparing a sample of 20 X 40 X 1 mm. The measuring device used was a nondestructive elastic modulus measuring system (Kanebo KI-11).
[0045] 硬度は、微小硬度計 (松沢精機製 MXT-50)を用いて 10回測定し、その平均を 算出した。 [0045] The hardness was measured 10 times using a micro hardness tester (MXT-50 manufactured by Matsuzawa Seiki Co., Ltd.), and the average was calculated.
[0046] 平均透過率は、 40 X 40 X 0. 7mmの試料を作製し、分光光度計(島津製作所製 UV-3100PC)を用いて波長 400〜700nmの各波長における透過率をスリット幅 2n
mで測定し、平均して算出した。 [0046] The average transmittance was 40 x 40 x 0.7 mm, and the transmittance at each wavelength of 400 to 700 nm was measured using a spectrophotometer (Shimadzu UV-3100PC) with a slit width of 2n. Measured in m and averaged.
[0047] 密度は、周知のアルキメデス法により測定した。熱膨張係数は、ディラトメーターを 用いて測定し、 30〜380°Cにおける平均熱膨張係数を用いた。 [0047] The density was measured by the well-known Archimedes method. The thermal expansion coefficient was measured using a dilatometer, and the average thermal expansion coefficient at 30 to 380 ° C was used.
[0048] 次に、橈み量を以下のようにして測定した。 [0048] Next, the amount of stagnation was measured as follows.
[0049] まず、表 2に示す各試料を用意し、試料の各辺が lmm幅で支持される枠に配設し た。 [0049] First, each sample shown in Table 2 was prepared and arranged on a frame in which each side of the sample was supported with a width of lmm.
[0050] 次に、試料の中央に、 10mm X 10mmの正方形断面を有する棒で試料表面と垂 直な方向に IONの荷重をカ卩え、その中央の変位量を橈み量として測定した。 [0050] Next, an ION load was measured in a direction perpendicular to the sample surface with a rod having a square cross section of 10 mm x 10 mm in the center of the sample, and the amount of displacement at the center was measured as the amount of stagnation.
[0051] 次に、実施例および比較例 1の試料を 35 X 35 X 0. 70mmの基板をそれぞれ 5枚 づっ用意し、表 3に記載の条件で硝酸カリウム融液中に浸漬した。 [0051] Next, five samples of 35 x 35 x 0.70 mm were prepared for the samples of Example and Comparative Example 1, respectively, and immersed in a potassium nitrate melt under the conditions shown in Table 3.
[0052] 表面応力計 (東芝製 FSM-60)を用いて試料表面に圧縮応力層が形成されてい ることを確認し、その圧縮応力値およびその深さを測定した。 [0052] Using a surface stress meter (FSM-60 manufactured by Toshiba), it was confirmed that a compressive stress layer was formed on the sample surface, and the compressive stress value and the depth thereof were measured.
[0053] また、浸漬した試料を内径 25mmの平滑なリング上に載置し、直径 12. 5mmの平 滑な圧子を用いて、試料の中央に破損するまで荷重をかけ、 5回の破壊荷重の平均 値を算出し平均破壊強度とした。 [0053] Also, the immersed sample was placed on a smooth ring with an inner diameter of 25 mm, and a load was applied to the center of the sample using a flat indenter with a diameter of 12.5 mm until it was damaged. Was calculated as the average fracture strength.
[0054] 表 1から明らかなように、実施例 1のヤング率は 81GPa、実施例 2のヤング率は 82G Paであり、比較例 1は 70GPaであった。 As is clear from Table 1, the Young's modulus of Example 1 was 81 GPa, the Young's modulus of Example 2 was 82 GPa, and Comparative Example 1 was 70 GPa.
[0055] また、表 2から明らかなように、同じサイズの試料において実施例は、比較例 1よりも 橈み量が小さ!/、。このため実施例は試料自体の薄肉化またはディスプレイとの間隔 を小さくできるため携帯機器の薄肉化に有効である。 [0055] Further, as is apparent from Table 2, in the same size sample, the stagnation amount of the example was smaller than that of Comparative Example 1! /. For this reason, since the embodiment can reduce the thickness of the sample itself or the distance from the display, it is effective for reducing the thickness of the portable device.
[0056] また、表 3から明らかなように、強化後の実施例 1および実施例 2は、強化後の比較 例 1よりも高い平均破壊強度であった。 [0056] As is clear from Table 3, Example 1 and Example 2 after strengthening had higher average fracture strength than Comparative Example 1 after strengthening.
また、実施例 1及び比較例 1について、 35 X 35 X 0. 5mmの板状試料を 500°Cに 設定した硝酸カリウム溶融塩に浸漬した。尚、これらの板状試料の全端面は # 600 の耐水研磨紙で研磨し、また両面は光学研磨してある。また、 1枚の板状試料が硝酸 カリウム溶融塩にその全体が浸漬するまでの時間は 1秒以内とし、実施例 1及び比較 例 1についてそれぞれ 50枚の板状試料の破損枚数を調べた。その結果、実施例 1 は、破損枚数が 50枚中 0枚であったのに対し、比較例 1は、破損枚数が 50枚中 5枚
あった。 For Example 1 and Comparative Example 1, a 35 × 35 × 0.5 mm plate-like sample was immersed in molten potassium nitrate set at 500 ° C. All the end surfaces of these plate samples were polished with # 600 water-resistant abrasive paper, and both surfaces were optically polished. In addition, the time until one plate-like sample was completely immersed in potassium nitrate molten salt was within 1 second, and the number of damaged plate samples for Example 1 and Comparative Example 1 was examined. As a result, in Example 1, the number of damaged sheets was 0 out of 50 sheets, whereas in Comparative Example 1, the number of damaged sheets was 5 out of 50 sheets. there were.
[0057] 本発明を特定の態様を参照して詳細に説明したが、本発明の精神と範囲を離れる ことなく様々な変更および修正が可能であることは、当業者にとって明らかである。 なお、本出願は、 2005年 10月 3日付けで出願された日本特許出願 (特願 2005— 289490)及び 2006年 9月 29日付けで出願された日本特許出願(特願 2006— 268 391)に基づいており、その全体が引用により援用される。 [0057] Although the invention has been described in detail with reference to specific embodiments, it will be apparent to those skilled in the art that various changes and modifications can be made without departing from the spirit and scope of the invention. This application consists of a Japanese patent application filed on October 3, 2005 (Japanese Patent Application 2005-289490) and a Japanese patent application filed on September 29, 2006 (Japanese Patent Application 2006-268 391). Which is incorporated by reference in its entirety.
また、ここに引用されるすべての参照は全体として取り込まれる。 Also, all references cited herein are incorporated as a whole.
産業上の利用可能性 Industrial applicability
[0058] 本発明の携帯機器表示装置用保護板は、携帯電話、デジタルカメラや PDAだけで なぐ例えば、携帯ゲーム機、ポータブル音楽プレヤー、 ICレコーダー、電子辞書等 のディスプレイの保護板として使用可能である。
[0058] The protective plate for a portable device display device of the present invention can be used as a protective plate for displays such as portable game machines, portable music players, IC recorders, electronic dictionaries, etc., which can be used only with a mobile phone, a digital camera, or a PDA. is there.
Claims
[1] ヤング率が 75GPa以上の板ガラスを備えてなることを特徴とする携帯機器表示装 置用保護板。 [1] A protective plate for a portable device display device, comprising a plate glass having a Young's modulus of 75 GPa or more.
[2] 板ガラスが物理強化または化学強化されて 、ることを特徴とする請求項 1に記載の 携帯機器表示装置用保護板。 [2] The protective plate for a mobile device display device according to [1], wherein the plate glass is physically strengthened or chemically strengthened.
[3] 板ガラスの表面圧縮応力値が 700MPa以上であることを特徴とする請求項 1または[3] The surface compressive stress value of the plate glass is 700 MPa or more, or 1
2に記載の携帯機器表示装置用保護板。 2. A protective plate for a portable device display device according to 2.
[4] 板ガラスの表面に飛散防止フィルムが貼付されてなることを特徴とする請求項 1〜3 の 、ずれかに記載の携帯機器表示装置用保護板。 [4] The protective plate for a portable device display device according to any one of claims 1 to 3, wherein an anti-scattering film is adhered to the surface of the plate glass.
[5] 質量%表示で、 SiO 50〜80%、Α1 Ο 15〜30%、 Al O +MgO+ZnO 15 [5] SiO 50-80%, Α1 Ο 15-30%, Al 2 O + MgO + ZnO 15
2 2 3 2 3 2 2 3 2 3
〜30%の組成を含有する板ガラスを備えてなることを特徴とする携帯機器表示装置 用保護板。 A protective plate for a portable device display device, comprising a plate glass containing a composition of -30%.
[6] 板ガラスが質量%表示で、 SiO 50〜80%、Α1 Ο 15〜30%、 Al O +MgO + [6] Sheet glass is expressed in mass%, SiO 50-80%, Α1 Ο 15-30%, Al O + MgO +
2 2 3 2 3 2 2 3 2 3
ZnO 15〜30%の糸且成を含有するガラス力もなることを特徴とする請求項 1〜4のい ずれかに記載の携帯機器表示装置用保護板。
The protective plate for a portable device display device according to any one of claims 1 to 4, wherein the protective plate has a glass strength containing 15-30% of ZnO.
Applications Claiming Priority (2)
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JP2006-268391 | 2006-09-29 | ||
JP2006268391A JP4793756B2 (en) | 2005-10-03 | 2006-09-29 | Protection plate for portable device display device |
Publications (1)
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WO2008050500A1 true WO2008050500A1 (en) | 2008-05-02 |
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ID=39324312
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PCT/JP2007/057482 WO2008050500A1 (en) | 2006-09-29 | 2007-04-03 | Protective plate for portable equipment display device |
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