Patent Application
20080211384
The present invention relates to an image display and a spacer used in the same.
Various types of so-called flat panel display (FPD) in which a flat rear substrate and a flat front substrate are laminated are known. For example, flat panel displays having electron emitters arranged in a matrix form draw attention, and as one of them, field emission displays (FED) utilizing minute integrative cold cathodes, and electron emission displays are known. Cathodes of these image displays use a Spindt-type electron emitter, a surface conductive type electron emitter, a carbon nanotube type electron emitter, or a thin film type electron emitter such as an MIM (Metal-Insulator-Metal) type obtained by laminating a metal, an insulator and a metal, an MIS (Metal-Insulator-Semiconductor) type obtained by laminating a metal, an insulator and a semiconductor, or a Metal-Insulator-Semiconductor-Metal type.
In emissive FPDs, a rear substrate equipped with electron emitters like those described above and a front substrate equipped with phosphor layers and an anode forming an acceleration voltage to cause electrons emitted from the electron emitters to impinge on the phosphor layers are laminated, and an internal space through which both the panels face each other is sealed in a predetermined vacuum state. The rear substrate is equipped with a large number of electron emitters in a matrix array, and the front substrate is equipped with phosphor layers and an anode forming an acceleration voltage to form an electric field to cause electrons emitted from the electron emitters to impinge on the phosphor layers.
An individual electron emitter makes a pair with a corresponding phosphor layer to constitute a unit pixel. Commonly, unit pixels of three colors, red (R), green (G) and blue (B), constitutes one pixel (color pixel). In the case of color pixels, a unit pixel is also called a subpixel.
The rear substrate and the front substrate are held with a predetermined gap by partition holding members called spacers arranged so as to hold both the substrates in a display region. The spacers comprise a plate formed of a member having a conductivity in some degree such as glass or ceramic, and are commonly installed in every plural pixels at positions where the operation of the pixels are not disturbed.
Spacers are arranged with an equal gap to keep two substrates parallel. As a spacer, one is know in which an antistatic film of 108 to 1010 Ω/□ in surface resistance is provided on the surface of an insulating glass substrate.
As the antistatic film, a film having conductive particles formed like islands on a high-resistance film is described in Patent Document 1; an alloy oxide film of a transition metal and cobalt or a nitride film in Patent Document 2; a film constituted of Cr, Al nitride and conductive particles in Patent Document 3; and a film whose substrate partially is exposed in Patent Document 4.
In an image display fabricated using spacers having an antistatic film on their surface, the spacers have no electrostatic charge, therefore, images are displayed with no curved orbit of electrons emitted from electron emitters.
However, an image display equipped with spacers has such a problem that the shadow of the spacer is silhouetted on a screen. The problem cannot be eliminated even in the image display having an antistatic film on its surface. The cause is the contamination of electron emitters by a spacer fixing frit to fix a spacer to a substrate.
A spacer is adhered to a front substrate using a spacer fixing frit and adhered or pressed to a rear substrate using a spacer fixing frit. Constituent elements of the spacer fixing frit propagate along the spacer surface, migrate and diffuse to electron emitters, and contaminate and deteriorate the electron emitters. Thereby, the shadow of the spacer is silhouetted on a screen.
As a spacer fixing frit, a mixture of a Pb-based glass frit with conductive particles has been conventionally used. However, according to the enforcement of the RoHS Directive, Pb-based glass frits cannot be used and V-based glasses, Sn-based glasses or Bi-based glasses have been recently used as alternatives.
However, use of lead-free glasses such as V-based glasses, Sn-based glasses or Bi-based glasses contaminates and deteriorates electron emitters by elements constituting the glass frit.
For example, when a spacer is fixed to a front substrate and a rear substrate using a lead-free glass, the number of electron emitters being deteriorated increases in the electron emitters between in the vicinity of the spacer and up to the third or fourth line, and consequently, the shadow of the spacer is silhouetted on a screen.
Further, for example, when a spacer is fixed to a front substrate side using a lead-free glass and is pressed and fixed on a rear substrate side having electron emitters, although the deterioration of the electron emitters is less than that in the above-mentioned example, electron emitters between in the vicinity of the spacer and up to the first or second line deteriorate, whereby the shadow of the spacer is silhouetted on a screen. This is because constituent elements of the lead-free glass present on the front substrate side propagate along the spacer surface and migrate to the rear substrate side.
Even when a Pb-based glass frit is used, ingredients constituting the glass frit similarly cause the contamination of electron emitters though not so much as in the use of a lead-free glass frit, whereby the shadow of the spacer is silhouetted on a screen.
It is an object of the present invention to provide a field emission display in which the propagation along the spacers and migration to electron emitters of constituent elements of a glass frit to fix spacers are suppressed; and the contamination of spacers and electron emitters by diffusion of a glass adhesive to fix the spacers is suppressed; and thereby providing high-quality images.
The featuring points of the present invention lie in the use of a glass containing crystal particles as a material for fabricating an image display. By attaching a glass having crystal particles to the surface of a spacer, or by using the glass as a glass adhesive to fix a spacer, the glass adhesive to fix the spacer is prevented from diffusing and contaminating the circumference.
A first aspect of the present invention is an image display comprising a rear substrate provided with electron emitters on its inner surface, a front substrate facing the rear substrate, provided on an inner surface thereof with phosphor layers having an array corresponding to the electron emitters, and having an outer surface serving as a display surface, glass-made spacers holding a gap between the rear substrate and the front substrate and adhered at least to the inner surface of the front substrate by using a spacer fixing frit; and a sealing frame sealing a periphery of a spacial part between the rear substrate and the front substrate, in which the oxide crystal particles are provided on a surface of the spacer.
Further, the present invention has a feature wherein the glass-made spacers holding the gap between the rear substrate and the front substrate in the image display have oxide crystal particles on their surfaces.
Any method for fixing the oxide crystal particles on the surfaces of the spacers can be used and is not limited. For example, a method may involve mounting the oxide crystal particles on the surface of a glass substrate constituting a spacer and heating to a softening temperature of the glass substrate to fix the particles. A method may involve fixing the oxide crystal particles to a spacer by using a glass adhesive. The method using a glass adhesive is preferable because the fixing operation of oxide crystal particles is easily carried out, and besides, the particles can surely be fixed.
Oxide crystal particles of not less than 0.1 μm and not more than 50 μm in particle size preferably account for not less than 90% of the oxide crystal particles on each spacer surface.
A covering rate with the oxide crystal particles of a spacer surface is preferably 10 to 100%.
A surface roughness of each spacer having the oxide crystal particles is preferably not less than 0.1 μm and not more than 50 μm.
An attachment form of the oxide crystal particles on each spacer surface may be one in which the particles are dispersed and disposed like isolated islands or may be one in which the particles are attached like continuous stripes as long as the above-mentioned conditions are satisfied.
A technique for attaching the oxide crystal particles on each spacer surface involves spray coating. This technique involves fabricating a spray liquid containing several percents to several tens percents of the oxide crystal particles and spraying the liquid to a spacer. The spray liquid may contain a glass ingredient to more firmly fix the oxide crystal particles.
In the case of fabricating the spacers in a drawing process of a glass preform, a glass perform on which oxide crystals are previously provided is drawn to obtain a spacer having the oxide crystal particles on its surface. For example, a paste containing the oxide crystal particles is printed like stripes, on a glass preform in advance, and a spacer on the surface of which the oxide crystal particles are disposed like stripes is thereby obtained. The paste containing the oxide crystal particles may contain a glass ingredient to more firmly fix the oxide crystal particles.
An oxide containing vanadium and phosphorus is remarkably preferable as the oxide crystal particles fixed on each spacer surface. Other examples of the oxide crystal particles preferably include those selected from CoO, CuO, Fe2O3, MnO, Zr2O3, Y2O3, Nd2O3, Gd2O3, ZnO, V2O5 and Sb2O5. These may be used alone or as a mixture.
A surface resistance of each spacer having the oxide crystal particles on its surface is preferably in the range of 108 to 1012 Ω/□.
The oxide crystal particles fixed on each spacer surface function as an obstacle to obstruct the propagation along the spacers and the migration and diffusion to the electron emitters of elements constituting the spacer fixing frit. Thereby, the elements constituting the spacer fixing frit are prevented from moving and deteriorating the electron emitters and the decrease in the image quality caused by this can be prevented.
A second aspect of the present invention is a field emission display comprising a rear panel comprising a glass substrate on which electron emitters to emit electrons are formed; a front panel comprising a glass substrate on which phosphors to emit light by irradiation of an electron beam are formed; and a plurality of spacers arranged between the front panel and the rear panel wherein the spacers are conductive and at least partially fixed to the front panel by an adhesive layer comprising a partially crystallized glass.
The feature of the present invention lies in that when a spacer is fixed, a glass adhesive containing amorphous glass portions and crystalline portions, i.e., crystal phase portions is used.
The crystalline portions have a higher melting point than the amorphous glass portions, and function to reduce the diffusion of the adhesive. Further, since constituent elements of the crystal phase are more strongly bound to the base material of the adhesive than constituent elements of the amorphous glass, the dissociation and scatter of the glass constituent elements can be prevented and the contamination of the spacers and the electron emitters can be reduced. Therefore, the more content of the crystal phase gives a glass adhesive with less contamination. It is especially preferable that the content of the crystal phase be not less than 50 vol % and not more than 95 vol %.
Fixing of the spacers using a glass frit or a glass paste as a raw material of an adhesive is an easy way. In this case, the adhesive is preferably a glass which does not contain crystals at the stage of frit and the like and in which crystals are deposited when the glass melts by heat when the spacers are fixed. As a result, the strength of the spacer fixation can be held and the diffusion of the adhesive can be prevented.
Here, the glass frit means a glass powder obtained by blending raw materials of a glass, melting them at a high temperature and then quenching the melt, and the glass paste means a mixture of a frit and a liquid ingredient.
The adhesive and the glass frit for fixing the spacers in the present invention preferably contains V2O5 or V2O5 and P2O5 as main ingredients. The glass frit is especially preferably a glass containing, at least, V2O5 at 50 to 60 wt %, P2O5 at 15 to 25 wt % and ZnO at 10 to 30 wt %. For making a conductive glass, V2O5 is necessary. Deviation of V2O5 and P2O5 from the above range does not form a glass. ZnO is contained for adjusting the electric resistance of the glass and promoting the crystallization. With ZnO at less than 10 wt %, the crystallization is insufficient, and with ZnO exceeding 30 wt %, the adhesive force of the spacers decreases.
The adhesive has an electric resistivity of not more than 109 Ωcm and is made of a glass at least a part of which is crystallized. Ordinal glass spacers have an electric resistivity of 109 Ωcm; by contrast, wiring formed on a glass substrate constituting a rear panel has an electric resistivity of 0 Ωcm. Therefore, the adhesive preferably has an electric resistivity of more than 0 Ωcm and less than 109 Ωcm for preventing the electrification of the spacers.
The present invention provides a glass frit comprising a glass ingredient constituting a conductive glass and a crystallizing ingredient to react with a part of the glass constituting ingredient and form a crystal phase. The glass frit of the present invention preferably contains V2O5 at 50 to 60 wt %, P2O5 at 15 to 25 wt % and ZnO at 10 to 30 wt % in terms of oxide.
According to the present invention, by making the most of crystal particles and applying them to either one or both of a spacer surface and a spacer fixing frit, the contamination and deterioration of electron emitters by the migration and diffusion of elements constituting the spacer fixing frit can be suppressed and the decrease in the image quality caused by this can be improved.
Other objects, features and advantages of the invention will become apparent from the following description of the embodiments of the invention taken in conjunction with the accompanying drawings.
Hereinafter, preferred embodiments of the present invention will be described in detail referring to the drawings. In the following description, a front substrate is also referred to as a panel.
A flat panel display described in the following examples is only an example, and the present invention can also be applied to various types of flat panel displays using a glass plate on which wiring is formed, such as displays of electron emission type or field emission type using thin film electron emitters, and plasma displays.
In this example, a constitution of a flat panel display will be described.
In
A front substrate 200 is a little smaller than the rear substrate 100. Wirings dT which are lead out terminals of the image signal wirings d and wirings ST which are lead out terminals of the scanning signal wirings S are formed on marginal surfaces of the rear substrate 100 jutting out from the front substrate 200. Phosphor layers of three colors 210 (210(R), 210(G) and 210(B)) are formed on the inner surface of the front substrate 200, and anode 220 is formed thereon. Reference numeral 410 denotes an image signal line drive circuit; and 420 denotes an operational signal line drive circuit.
In this example, the phosphor layers 210 (210(R), 210(G) and 210(B)) are partitioned by a light shielding layer (black matrix) 230. Here, the anode 220 is illustrated as a solid electrode, but may be a stripe-shaped electrode which crosses the scanning signal wirings S (S1, S2, S3, . . . Sm) and is divided electrodes for every pixels column.
Electrons emitted from each electron emitter 110 are accelerated and impinged on each phosphor layer 210 (210(R), 210(G) or 210(B)) constituting a corresponding subpixel. Thereby, each phosphor layer 210 emits light of a predetermined color and the color is mixed with emitted light colors of the other subpixels, thus constituting color pixels of predetermined colors.
As shown in
As described in
On the other hand, on the inner surface of the front substrate 200, the anode 220 and the phosphor layers 210 are formed as films. As the anode 220, an aluminum layer is generally used. A power feed line of the anode 220 reaches the rear substrate 100 through a connection conductor between the substrates, not shown in the figure, and is led out as a lead out terminal (wiring) from an appropriate part of the rear substrate 100 to the outside of the sealing region which is a part where the sealing frame is installed.
The inner surfaces of the front substrate 200 and the rear substrate 100 face each other and the periphery of the substrates are fixed using the sealing glass frit 310 such that an internal space interposed between both the substrates is isolated from the outside. When the fixation using the sealing glass frit 310 is carried out, heating at about 400° C., for example, is conducted. Thereafter, the interior of the display is evacuated to about 1 μPa through an exhaust pipe 320 and then sealed up. In the operation, a voltage of about 2 to 10 kV is applied to the anode 220 of the front substrate.
In the display of this example, a structure using MIM for the electron emitters is adopted as an example, but the present invention is not limited thereto and as described above, the present invention can be applied similarly to flat panel displays using any of various electron emitters.
A constitution may be adopted in which the front substrate 200 is made of a brim-shaped dish shape in which a brim bent and protruded from the periphery thereof toward the rear substrate 100 side is formed, and a frit glass is applied on the contacting part of the brim and the rear substrate to seal both the substrates. In this case, the application of the frit glass is on the rear substrate side only.
Spacers 150 to hold a gap between the rear substrate and the front substrate are fixed using the front substrate 200 and a spacer fixing glass. The spacers are fixed to the rear substrate 100 by using the spacer fixing glass, or are brought into contact thereto by directly pressing the spacers on the scanning signal wirings S without using the spacer fixing glass.
In Example 2, an example of a case where crystal particles are applied on a spacer surface will be in detail described.
The attachment form of the oxide crystal particles 155 may be a form (
When the spacers are fabricated by a drawing process of a glass preform, the oxide crystal particles are previously provided on a glass preform, and the preform is drawn to obtain the spacers having the oxide crystal particles on their surfaces.
The spacer used in this example is a glass spacer of 3 mm in width, 100 μm in thickness and 100 mm in length obtained by drawing a glass containing 20 wt % of V2O5, 30 wt % of P2O5, 30 wt % of WO3 and 20 wt % of BaO by the redrawing method.
A spacer fixing glass was a glass containing 62 wt % of V2O5, 25 wt % of P2O5, 3 wt % of WO3, 5 wt % of BaO and 5 wt % of Sb2O3.
The starting raw materials of these glasses were V2O5 (made by Kojundo Chemical Laboratory Co., Ltd., purity: 99.9%), WO3 (made by Kojundo Chemical Laboratory Co., Ltd., purity: 99.9%), BaCO3 (made by Kojundo Chemical Laboratory Co., Ltd., purity: 99.9%), P2O5 (made by Kojundo Chemical Laboratory Co., Ltd., purity: 99.9%) and Sb2O3. (made by Wako Pure Chemical Industries, Ltd., purity: 99.9%).
The oxide crystal particles to be coated on the glass spacers were an oxide powder, a vanadic phosphoric acid-based crystallized glass and the like. A vanadic phosphoric acid-based glass powder was adopted as a comparative example.
In this example, studies were conducted using the spray atomizing method with which spacers having oxide crystal particles on their surface were easily fabricated. The particles of each kind were pulverized to an average particle size of 0.1 μm and mixed with a solvent PGME in a proportion of 3% in terms of solid content to make spray atomizing liquids.
The spray atomizing liquid was sprayed on the spacers to fabricate spacers coated in different thicknesses. The spacers after the spray coating were baked in the atmosphere at 460° C. for 30 min to adhere the oxide crystal particles attached on the spacer surfaces by using a glass.
Oxide crystal particles used in the various kinds of spray atomizing liquids fabricated for spray coating and spray atomizing conditions, and results of evaluations of spray coating thicknesses, surface roughnesses Ra and surface resistances at room temperature and at 80° C. are collectively shown in
Out of these spacers, spacers having a surface resistance of not less than 108 Ω/□ were fixed on the scanning wirings S of the front substrate by using the spacer fixing glass to fabricate flat panel displays shown in
A voltage of 10 kV was applied to the panels to light and the deterioration of the electron emitters EM due to a long-time lighting was observed.
By 10-hour lighting, in the panels using some spacers, the image luminance in the vicinity of the spacers became dark and shadows of the spacers were observed. The results are collectively shown in
Out of these samples, two samples having the most severe deterioration of the electron emitters and one sample having no deterioration were chosen and currents flowing in the electron emitters and emission currents Ies were measured. Ie right after a voltage of 10 kV was applied to the panels for lighting and Ie after 10-hour lighting were evaluated. The positional relation of the spacer positions and the electron emitters whose Ies had been evaluated is shown in
The panels were disassembled and analyzed for ingredients of the spacer fixing glass having diffused in the electron emitters in the vicinity of the spacers by the TOF-SIMS method, and vanadium and phosphorus were detected from the first lines of the vicinity of the spacers. Vanadium and phosphorus were detected from the second and successive lines though decreasing gradually.
By contrast, the samples in which the deterioration of the electron emitters Em was not confirmed had no detection of vanadium and phosphorus in the vicinity of the spacers. The evaluation results by the TOF-SIMS method are shown in
That is, the panels on which the spacers coated with the oxide crystal particles on their surface were mounted exhibited no deterioration of the electron emitters.
Separate studies on panels on which the spacers coated with a crystallized glass obtained by crystallizing a vanadic phosphoric acid glass exhibited good results and no deterioration of the electron emitters. That is, as a coating for preventing deterioration of electron emitters, coating of a crystal or a crystallized glass is effective, and the contamination of electron emitters by a spacer fixing glass can be thereby prevented.
The spacers which otherwise were not allowed to be mounted on a panel are allowed to be mounted by fitting the surface resistance to not less than 108 Ω/□ by adjusting the coating film thickness.
This example used a WO3—V2O3—P2O5 glass as a spacer material and a V2O3—P2O5 glass as a spacer fixing glass, but the present invention is not essentially limited to these types of glasses.
In Example 3, an example in which crystal particles were applied to a spacer fixing frit will be in detail described.
This display is configured with the rear panel and the front panel facing each other with a predetermined gap. The rear panel had the first glass substrate 401 on the inner surface of which a large number of electron emitters (cathode) are formed. The front panel has the transparent second glass substrate 402 in which the phosphors of plural colors which are partitioned from one another with a black matrix film and the anode are formed on the inner surface of the second glass substrate 402 facing the cathode-formed surface of the first glass substrate 401.
The first glass substrate 401 and the second glass substrate 402 face each other with a predetermined gap through spacers 150 being gap holding members. The spacers 150 are adhered and fixed to the second glass substrate 402 by adhering a part of or the entire of the contacting interface by an adhesive layer comprising a conductive glass. The other end surfaces, i.e., the end surfaces contacting with the first glass substrate, of the spacers 150 are pressed and abutted on the first glass substrate without using an adhesive.
Since very sensitive elements are arrayed on the cathode side, the frit to fix the spacers is not used and a state in which the spacers are pressed on is adopted.
The adhesive layer (sealing frit glass) 105 is applied on the inner peripheral parts of the first glass substrate 401 and the second glass substrate 402 and the substrates with the sealing glass frame 300 interposed therebetween are baked and fixed to from the closed container. The interior of the closed container is evacuated through an exhaust pipe not shown in the figure. Images are displayed in a display area AR.
A method of fixing the spacer to the second glass substrate by using an adhesive will be described.
An adhesive constituting the adhesive layer 403 in
A glass frit contains ingredients constituting a glass and ingredients constituting a crystal phase, and besides these, it can be further mixed with fillers. The fillers are those which improve various characteristics of the adhesive such as thermal expansion coefficient, sealing temperature, electric resistance value and wettability with members constituting a display. The proportion of a sealing glass and fillers contained in a glass frit can be adjusted according to the purposes, but it is preferable that the sealing glass be 20 to 90 vol % and the fillers are 10 to 80 vol %. Plural kinds of fillers having different properties such as thermal expansion coefficient can be together used. The fillers are preferably granular metals and inorganic oxides. Inorganic oxides include, for example, SiO2, ZrO2, Al2O3, ZrSiO4, cordierite, mullite and eucryptite. The particle size of fillers is preferably in the range of 0.5 to 10 μm, especially preferably 1 to 5 μm. Mixing of such small filler particles or increasing the filler amount can prevent the adhesive from being sucked in due to the interior reduced-pressure condition when the adhesive is heated and adhered, because the viscosity of the adhesive increases.
The fillers can be used as a mixture of plural kinds according to characteristics of interest. SiO2 is effective for adjusting the thermal expansion coefficient because it has a smaller thermal expansion coefficient than glasses comprising vanadium and phosphorus as main ingredients. Al2O3 can reduce the cost by adjusting the viscosity by mixing or increasing the adhesive amount because Al2O3 has the nearly same thermal expansion coefficient as glasses comprising vanadium and phosphorus as main ingredients. Mixing a filler like crystalline particles having a higher thermal conductivity than a sealing glass can raise the thermal conductivity of an adhesive and make adhesion easier.
An example of a method of using the glass adhesive described above when a spacer is fixed to a glass substrate, for example, at 450° C. will be described hereinafter.
The glass adhesive described above is not limited to the usage as an adhesive for fixing a spacer to a glass substrate, and can be widely used as an adhering frit glass.
In this example, the spacers 150 were fixed to a front panel by using the glass frit of the present invention as follows.
The compositions of the glass frits are shown in Table 1. The glass to become a base material was fabricated as follows.
The starting raw materials of these glass base materials were V2O5 (made by Kojundo Chemical Laboratory Co., Ltd., purity: 99.9%), BaCO3 (made by Kojundo Chemical Laboratory Co., Ltd., purity: 99.9%), P2O5 (made by Kojundo Chemical Laboratory Co., Ltd., purity: 99.9%), ZnO (made by Kojundo Chemical Laboratory Co., Ltd., purity: 99.9%) and Sb2O3 (made by Wako Pure Chemical Industries, Ltd., purity: 99.9%). ZnO reacts with phosphorus in the glass ingredients on fixation of the spacers to form zinc phosphate and to deposit as a crystal phase.
The mixing proportion of the raw materials other than ZnO was 50 wt % of V2O5, 20 wt % of P2O5, 20 wt % of Sb2O3 and 10 wt % of BaO. BaCO3 was mixed by converting the corresponding amount of BaO taking into consideration of the decomposition into BaO+CO2. Each raw material was pulverized so as to have an average particle size of 1 μm.
First, the raw materials other than P2O5 and ZnO were mixed. This is because since P2O5 has a high hygroscopicity, it is not left in the air for a long time. The mixed powder other than P2O5 and ZnO was charged in a platinum crucible and was put on a balance together with the crucible. Then, P2O5 of a predetermined amount was weighed and mixed with the mixed powder by a metal-made spoon. At this time, for avoiding moisture absorption from the air, mixing using a mortal or a ball mill was not performed.
The platinum crucible charged with the raw material mixed powder was installed in a glass melting furnace and started to be heated. The temperature rising rate was set at 5° C./min and the temperature was kept for 1 hour after a target temperature was reached. In this example, the target temperature was fixed at 1,000° C. The melted glass was held for 1 hour while stirred, and after the holding, the platinum crucible was taken out the melting furnace and the melted glass was pored in a graphite mold to quench the melted glass.
Thermal characteristics of the obtained glass are shown in Table 2. The temperature on fixing the spacers using the glass frit was set at 450° C. in consideration of the softening temperature of the glass.
The obtained glass base material was pulverized to an average particle size of 5 μm (maximum particle size: 10 μm), and then, ZnO (average particle size: 1 μm) to crystallize the glasses was mixed in the proportions shown in Table 1.
The mixed powders were each shaped into 10 mm in diameter and 5 mm in thickness, heat-treated at 450° C. for 30 min, and generated crystal phases were identified by an X-ray diffractometer. As a result, it was found that the sample added with more ZnO had a larger proportion of the generated crystal phase, that is, a less amount of the glass remained in the glass frit.
The mixed powder, a solvent and a binder were mixed to be made into a paste, and the paste was applied as a glass frit for fixing spacers when a panel shown in
A display having a structure shown in
Further, in the range of the loading amount of ZnO from 10 to 23 wt %, no shadows of the spacers were viewed and a display providing high-quality images could be obtained.
In this example, although ZnO was used as an ingredient to react with a part of glass ingredients and deposit crystal phases, MgO may be used instead. MgO reacts with phosphorus in glass ingredients and forms magnesium phosphate, and the magnesium phosphate deposits as crystal phases. However, since magnesium phosphate has a higher crystallization temperature than zinc phosphate, when MgO is used, a higher heating temperature is necessary on fixing spacers than in the case of using ZnO. Further, use of ZrO2 in place of ZnO gives the similar effect.
In this example, a glass base material of 50 wt % of V2O5, 20 wt % of P2O5, 20 wt % of Sb2O3 and 10 wt % of BaO was used, but it is not limited thereto.
It should be further understood by those skilled in the art that although the foregoing description has been made on embodiments of the invention, the invention is not limited thereto and various changes and modifications may be made without departing from the spirit of the invention and the scope of the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2007-022943 | Feb 2007 | JP | national |
| 2007-051387 | Mar 2007 | JP | national |
