CN1673142A - Bulkhead forming material for plasma display device - Google Patents

Bulkhead forming material for plasma display device Download PDF

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Publication number
CN1673142A
CN1673142A CNA2005100569259A CN200510056925A CN1673142A CN 1673142 A CN1673142 A CN 1673142A CN A2005100569259 A CNA2005100569259 A CN A2005100569259A CN 200510056925 A CN200510056925 A CN 200510056925A CN 1673142 A CN1673142 A CN 1673142A
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Prior art keywords
next door
plasma display
glass
display panel
zno
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CN100569684C (en
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小松谷俊介
大下浩之
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Nippon Electric Glass Co Ltd
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Nippon Electric Glass Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C14/00Glass compositions containing a non-glass component, e.g. compositions containing fibres, filaments, whiskers, platelets, or the like, dispersed in a glass matrix
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C3/00Glass compositions
    • C03C3/04Glass compositions containing silica
    • C03C3/062Glass compositions containing silica with less than 40% silica by weight
    • C03C3/064Glass compositions containing silica with less than 40% silica by weight containing boron
    • C03C3/066Glass compositions containing silica with less than 40% silica by weight containing boron containing zinc
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C4/00Compositions for glass with special properties
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL 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
    • C03C8/00Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
    • C03C8/24Fusion seal compositions being frit compositions having non-frit additions, i.e. for use as seals between dissimilar materials, e.g. glass and metal; Glass solders

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Ceramic Engineering (AREA)
  • Dispersion Chemistry (AREA)
  • Glass Compositions (AREA)
  • Gas-Filled Discharge Tubes (AREA)

Abstract

Provided is a material for forming a partition for a plasma display panel ,characterized by containing a ZnO-B<SB>2</SB>O<SB>3</SB>-based glass powder of 60-90 mass% and a filler powder of 10-40 mass%, where 20-100 mass% of the filler powder is a mullite powder. The ZnO-B<SB>2</SB>O<SB>3</SB>-based glass powder preferably contains, by mass%, 30-60% ZnO, 15-35% B<SB>2</SB>O<SB>3</SB>, 0-25% BaO, 3-20% SiO<SB>2</SB>, 0.5-6% Li<SB>2</SB>O, and 1-12% Li<SB>2</SB>O+Na<SB>2</SB>O+K<SB>2</SB>O.

Description

Plasma display forms material with the next door
Technical field
The present invention relates to a kind of plasma display panel and form material with the next door.
Background technology
Plasma display panel is the flat display board of self light emitting-type, has excellent characteristic such as light weight is slim, high angle of visibility, and pictureization greatly, so extremely gaze at as a kind of of the display unit of tool future.
Plasma display panel normally is provided with front glass substrate and back side glass substrate subtend, and a plurality of next doors that are formed for separating geseous discharge portion in the space between these substrates (are also referred to as barrier wall: barrier rib).With regard to the material that forms the next door, be extensive use of the material of hybrid glass powder and ceramic powder.This next door forms material in order to prevent the distortion of glass substrate, must under 600 ℃, fire, for this reason, concerning glass powder, use contains the glass as the PbO of the composition that reduces softening temperature, but there is the problem of harmful and offal treatment when making glass powder in the glass that contains PbO.Therefore, multiple use ZnO-B is disclosed 2O 3The plasma display panel of class glass powder forms material (for example the spy opens the 2002-326839 communique) with the next door.
And in order to improve the briliancy of plasma display panel, the next door with light transmission is adopted in expectation.Therefore, spy's a kind of material that can form next door of having opened the motion of 2002-110035 communique with light transmission.This material is to use the material of the alumina powder of specified particle size as the stopping composition powder.
The spy opens the 2002-110035 communique and opens the content of showing and be: as long as add alumina powder to ZnO-B 2O 3In the glass frit end, just can obtain having the next door of light transmission.But, with regard to ZnO-B 2O 3The glass frit end, the situation that can utilize the spy to open the technology of 2002-110035 communique is restricted.For example, the spy opens the ZnO-B of 2002-110035 communique 2O 3A large amount of BaO is contained at the glass frit end, and for the poor glass powder of BaO, even also be difficult to make the next door with light transmission with the alumina powder combination.
Summary of the invention
Even the object of the present invention is to provide a kind of at the poor ZnO-B of use BaO 2O 3Under the situation at glass frit end, also the plasma display panel that can form the next door with light transmission forms material with the next door.
Plasma display panel of the present invention forms material with the next door and is characterised in that, comprising: ZnO-B 2O 3Glass frit end 60~90 quality % and stopping composition powder 10~40 quality %, wherein mullite powders accounts for 20~100 quality % of above-mentioned stopping composition powder.
In one embodiment of the present invention, 50% median size of mullite powders is preferably 0.5~6 μ m.
In another embodiment of the invention, ZnO-B 2O 3It is that 30 quality % are above, B that ZnO is preferably contained at the glass frit end 2O 3Be more than the 15 quality %.And preferred BaO content is no more than 25 quality %.
In another embodiment of the invention, ZnO-B 2O 3The glass frit end preferably is made of crown glass.
In another kind of preferred embodiment of the present invention, ZnO-B 2O 3The glass frit end, in Quality Percentage, preferably ZnO is 30~60%, B by containing 2O 3Be 15~35%, BaO is 0~25%, SiO 2Be 3~20%, Li 2O is 0.5~6%, Li 2O+Na 2O+K 2O is 1~12% glass formation.
And next door of the present invention forms with mashed prod and next door and forms with embryo sheet (greensheet), it is characterized in that, contains above-mentioned materials.
And next door of the present invention is characterized in that, uses above-mentioned materials, above-mentioned mashed prod or above-mentioned embryo sheet and forms.
In one embodiment of the present invention, the next door of the formation diffusion transmitance value that is scaled the 550nm of thickness 30 μ m is counted more than 50% with the transmitance value that enters glass substrate.
Moreover, ZnO-B of the present invention 2O 3The glass frit end is low because of the specific inductivity of two materials with the composition material of mullite powders, so can form the next door of low specific inductivity (ε is below 10).Just because of this, also can be fit to be used in the next door that requires low specific inductivity.
It is not only can guarantee shape maintains but also can form the material with high permeability next door that plasma display panel of the present invention forms material with the next door.Therefore, be suitable as and be used to make the next door material that does not contain the high plasma display panel of lead and briliancy.
Embodiment
Investigation by the inventor etc. is learnt: when using mullite powders when replacing alumina powder, even using the poor ZnO-B of BaO 2O 3Under the situation at glass frit end, also can form next door with light transmission.Thus, infer that this is because this ZnO-B 2O 3Be that glass has the specific refractory power that ratio aluminum oxide more approaches mullite easily.
Below, be described in detail next door of the present invention and form material.
Plasma display panel of the present invention forms material with the next door and comprises ZnO-B 2O 3Glass frit end and stopping composition powder.Both ratios are ZnO-B 2O 3The glass frit end is that 60~90 quality %, stopping composition powder are 10~40 quality %, is preferably ZnO-B 2O 3The glass frit end is that 60~85 quality %, stopping composition powder are 15~40 quality %, more preferably ZnO-B 2O 3The glass frit end is that 63~84 quality %, stopping composition powder are 16~37 quality %.When (promptly when glass powder for a long time) the shape maintains reduction after a little while of stopping composition powder.On the other hand, be not easy to guarantee sufficient coking property, be difficult to form fine and close next door when the stopping composition powder becomes for a long time (be glass powder after a little while).And the light transmission in the next door that obtains also reduces.
Moreover material of the present invention mainly uses mullite powders as the stopping composition powder.Mullite powders can be used any of the product that burn till of aluminum oxide and silica or electric smelting product, in order to remove foreign matter etc., though the degree of sintering mullite powders not for example 300~1300 ℃, burn till in particularly preferably in 300~1100 ℃ scope also no problem.In addition, in the present invention, also can all use mullite powders, but in the scope of not damaging light transmission, also can use simultaneously with other stopping composition powder as the stopping composition powder.For example, also can import ceramic powder fillers such as aluminum oxide, silica in order to adjust thermal expansivity.And, in order to improve shape maintains, beyond alumina, the silica, also can import ceramic stopping composition such as trichroite.Mullite powders shared ratio in the stopping composition powder is all is 20~100 quality %, be preferably 25~100 quality %, 30~100 quality % more preferably.When the shared ratio of mullite powders hour, the light transmission in the next door that obtains reduces.
50% median size of mullite powders used in the present invention is preferably 0.5~6 μ m, is preferably 0.6~5 μ m especially.When the median size of mullite powders is too small, in the process of supplying with the mashed prod form, be difficult to adjust rheological property, and cost uprises also.On the other hand, when median size becomes big, the tendency of shape maintenance variation is arranged.In addition, also can mix the above mullite of two different kinds of median size with any mixture ratio.Moreover, with regard to the stopping composition powder beyond the mullite,, preferably use the stopping composition powder of 50% median size at 0.5~6 mu m range based on the reason same with mullite.But, because when using titanium dioxide, the light transmission in obvious damage next door is not so should use in the present invention.
ZnO-B used in the present invention 2O 3The glass frit end is to contain ZnO and B 2O 3Glass for major ingredient.Such glass is that for example ZnO content is the above and B of 30 quality % 2O 3Content is the above glass of 15 quality %.Even and be preferably and do not contain BaO or containing the glass that also is no more than the composition of 25 quality % under the situation of BaO.Its reason is to be favourable because compare when the glass of this scope make up with mullite powders on the next door of making light transmission excellence with alumina powder.Moreover, based on cutting down from the such purpose of the PbO of next door material, with PbO be below the 1 quality % for well, be not preferably at all and contain.
With regard to ZnO-B 2O 3Be the preferred group precedent of glass, can enumerate and contain in Quality Percentage that ZnO is 30~60%, B 2O 3Be 15~35%, BaO is 0~25%, SiO 2Be 3~20%, Li 2O is 0.5~6%, Li 2O+Na 2O+K 2O is 1~12% BaO-ZnO-B 2O 3Be glass.Glass with above-mentioned composition can be produced on the next door material that can burn till especially below 600 ℃ under the low temperature about 560 ℃.Below each composition is described.
ZnO is the composition that when reducing softening temperature thermal expansivity is reduced, and its content is 30~60%, is preferably 35~55%, more preferably 37~54%.When ZnO less than 30% the time, can not obtain above-mentioned effect; When greater than 60% the time, in glass, separate out crystallization, can not get fine and close sintered compact.
B 2O 3Be the composition that constitutes the glass skeleton, its content is 15~35%, is preferably 16~33%.Work as B 2O 3Less than 15% o'clock, be difficult to vitrifying; On the other hand, work as B 2O 3Greater than 35% o'clock, it is too high that softening temperature becomes, and when burning till under the temperature below 560 ℃, can not get fine and close sintered compact, and the display panel characteristic also reduces.
BaO is the composition that makes stabilization, and its content is 0~25%, is preferably 3~25%, more preferably 4~23%, is preferably 5~20% especially.BaO is not essential composition, but when less than 3% the time, the glass instability is easy to generate crystallization, has problems with the fitting tightly property of dry film, when forming material as the next door and burn till, thereby can not get the sintered compact of densification because of separating out crystallization.When greater than 25% the time, thermal expansivity uprises, and is not suitable for glass substrate, and light transmission reduces, so not preferred.
SiO 2Be the composition that forms the glass skeleton, its content is 3~20%, is preferably 4~17%, more preferably 4~16%.Work as SiO 2Less than 3% o'clock, the glass instability; When greater than 20% the time, it is too high that softening temperature becomes, and can not burn till under the temperature below 560 ℃.
Li 2O is the significantly reduced composition of softening temperature that makes glass, and its content is 0.2~6%, is preferably 0.5~5%.Work as Li 2O is less than 0.2% o'clock, because fully do not reduce softening temperature, so be difficult to burn till under the temperature below 560 ℃.On the other hand, work as Li 2O was greater than 6% o'clock, and glass is obviously unstable, is easy to generate crystallization, with the fitting tightly property reduction of dry film, when burning till as next door formation material, thereby can not get fine and close sintered compact because of separating out crystallization.
In addition, in order to keep the stability of glass, can not be with Li 2Under the situation of O heavy addition in the glass, preferably use and Li 2Composition---the Na that O equally makes the softening temperature of glass reduce 2O or K 2O or use both simultaneously.But, work as Na 2O, K 2The content of O for a long time, have stability, glass reduce, with the fitting tightly property reduction of dry film, can not get the anxiety of fine and close sintered body, so expectation Na 2O content is limited in below 9%, is preferably below 8%, is preferably below 6% especially, expectation K 2O content is limited in below 6%, is preferably below 5% especially.
With regard to the alkali composition, with Li 2O, Na 2O and K 2The total amount of O is calculated, and to need content be 1~12%, be preferably 2~10%.When the total amount less than 1% the time, because the softening temperature of glass is fully reduced, so can not under the temperature below 560 ℃, burn till.On the other hand, when greater than 12% the time, the glass instability, crystallization has easily reduced the fitting tightly property with dry film, and the weather resistance of glass has problems.
When adding the basic metal composition, the tendency with the fitting tightly property reduction of dry film is arranged.Therefore, in order to improve fitting tightly property, also can contain Al 2O 3But, work as Al 2O 3Contain quantitative change for a long time, softening temperature rises, so be preferably limited to below 1.5%.
Moreover, in order to make stabilizationization, preferred BaO/ (B 2O 3+ SiO 2) ratio in 0.1~0.8 scope.When this ratio less than 0.1 the time, it is unstable that glass becomes, and when forming material as the next door and burn till, is difficult to obtain the sintered compact of densification because of separating out crystallization.In addition, when greater than 0.8 the time, the next door forms the material coefficient of thermal expansion coefficient and uprises, and is difficult to be suitable for glass substrate.Preferred scope is 0.15~0.6.
Moreover, except that above-mentioned composition, in the scope of not damaging effect of the present invention, can add other composition.For example, in order to improve water tolerance or resistance to chemical reagents, can add alkaline earth metal oxide or Ta such as MgO, CaO, SrO 2O 5, La 2O 3, SnO 2, ZrO 2, TiO 2, Nb 2O 5, and, for stabilizationization, also can add P 2O 5In addition, the addition of these compositions is preferably and is limited in below 15%, is preferably below 14%, more preferably below 12%, be preferably below 10% especially to close quantifier.
Plasma display panel of the present invention forms material with the next door and can use with forms such as mashed prod or embryo sheets.
When using, form material with above-mentioned next door and use thermoplastic resin, plasticizer, solvent etc. with the mashed prod form.With regard to the content in the mashed prod of next door formation material, be generally about 30~90 quality %.With regard to the viscosity of mashed prod, be desirably 200~1500 pools.When viscosity is 200 pools when following, generation problem in the keeping of mashed prod is moored when above 1500 when viscosity, can have problems on the printing.Moreover, when providing for the state below 1000 pools,, preferably add 0~3% oxidation inhibitor or tensio-active agent for separation, the viscosity that prevents mashed prod reduces, the deterioration of resin equals possible trouble with mashed prod viscosity.In addition, so-called viscosity is meant under 23 ℃, sliding velocity are 5.7/ second condition and surveys periodic value among the present invention.
Thermoplastic resin is to improve dried film toughness and give the composition of flexibility, and its content is generally about 0.1~20 quality %.With regard to thermoplastic resin, can use poly-n-butyl methacrylate, polyvinyl butyral, polymethylmethacrylate, polyethyl methacrylate, ethyl cellulose etc., they use separately or mix use.
Plasticizer is a composition of giving the desciccator diaphragm flexibility in the control rate of drying, and its content is generally about 0~10 quality %.With regard to plasticizer, can use butyl benzyl phthalate, dioctyl phthalate (DOP), dimixo-octyl phthalate, dioctyl phthalate (DOP), dibutyl phthalate etc., they use separately or mix use.
Solvent is the material that is used to make the material pasty stateization, and its content is generally about 10~30 quality %.With regard to solvent, for example can enumerate terpinol, acetic acid glycol ether monobutyl ether-ether (diethylene glycol monobutyl ether acetate), single isopropylformic acid 2,2,4-trimethylammonium-1, the 3-pentadiol ester (2,2,4-trimethyl-1,3-pentadiol monoisobutyrate) etc., they can use or mix use separately.
The making of mashed prod be prepare the next door form material (glass powder and stopping composition powder), thermoplastic resin, plasticizer, solvent etc., by with the ratio of regulation mixing they can be used as mashed prod.
Use such mashed prod,, at first, use these mashed prod of coating such as silk screen print method or primary coating method, after then the use method of sandblasting is removed unwanted part, be fired into the next door of regulation shape for example in order to form the next door.
When using plasma display panel of the present invention to form material with the form of embryo sheet, form material with above-mentioned next door and use thermoplastic resin, plasticizer etc. with the next door.
The next door forms the content of material in the embryo sheet and is generally 60~80 quality %.
With regard to thermoplastic resin and plasticizer, can use and employed same thermoplastic resin and plasticizer when modulating above-mentioned mashed prod, with regard to the mixture ratio of thermoplastic resin, be generally about 5~30 quality %; With regard to the mixture ratio of plasticizer, be generally about 0~10 quality %.
With regard to the usual method of making the embryo sheet, preparing the next door forms material and thermoplastic resin and plasticizer and scrapes the skill in using a kitchen knife in cookery and carry out these slurries film shaped on polyethylene terephthalate thin slices such as (PET) to wherein adding auxiliary solvents such as main solvent such as toluene or Virahol with as slurries, utilizing.Thin slice is removed solvent or solvent by drying after being shaped, and can be used as the embryo sheet.
Behind the place that should form glass coating by the embryo sheet hot pressing that will obtain as described above and to burn till, can form glass coating.When forming the next door, the same after hot pressing and formed overlay with the situation of above-mentioned mashed prod, be processed into the next door shape of regulation.
In the above description, with regard to the formation method of next door, describe as example with the method that sandblasts of using mashed prod or embryo sheet, but be not limited to these methods, also be applicable to printing lamination method, ejaculation (lift off) method, photosensitivity mashed prod method, photosensitivity embryo sheet method, pressing etc. other the formation method and obtain material.
Light transmission is represented in the next door of above-mentioned such plasma display panel of making.With regard to the parameter of estimating light transmission, can utilize after the softening temperature of glass powder burns till 10 minutes, be converted into the diffusion transmitance value that thickness is the 550nm of 30 μ m.In the present invention, preferably this value is more than 50%, is in particular more than 55%.As long as this transmitance value is more than 50%, just can expect to improve the briliancy of plasma display panel.
Below, at length narrate the present invention based on embodiment.But the present invention is not limited to following embodiment.
Table 1 is that the employed glass powder of expression present embodiment forms that (table of test portion A~I), table 2 are the employed stopping composition powder of expression present embodiment (tables of test portion a~e).And, table 3~5th, the example (test portion No.1~24) of expression next door material and the table of its evaluation result.
Each test portion of table 1 is following to be modulated like that.At first, frits such as the various oxide compounds of forming shown in the blending table, carbonate behind the uniform mixing, are put into the back platinum crucible and 1250 ℃ of following fusions 2 hours, are obtained uniform vitreum.Then, pulverize vitreum with the alumina balls grinding machine, obtaining median size is that 3 μ m, maximum particle diameter are the glass powder of 20 μ m.
About the glass powder that obtains, measure its thermal expansivity, softening temperature.Consequently the thermal expansivity of each test portion of A~I is 69.3~83.0 * 10 -7/ ℃, softening temperature is below 564 ℃.
Table 1
????A ????B ????C ????D ????E ????F ????G ????H ????I
Glass is formed (quality %) ZnO B 2O 3??BaO ??SiO 2??Li 2O ??Na 2O ??K 2O ??Al 2O 3? ??TiO 2??Nb 2O 5??PbO ? ? ??CaO ??La 2O 3? ? ? ????50 ????24 ????12 ????8 ????3 ????- ????- ????1 ? ????2 ????- ????- ? ? ????- ????- ? ? ? ????52 ????26 ????9 ????9 ????2 ????- ????2 ????- ? ????- ????- ????- ? ? ????- ????- ? ? ? ????47 ????25 ????13 ????8 ????2 ????1 ????1 ????1 ? ????1 ????1 ????- ? ? ????- ????- ? ? ? ????45 ????30 ????15 ????6 ????2 ????2 ????- ????- ? ????- ????- ????- ? ? ????- ????- ? ? ? ????50 ????20 ????12 ????12 ????1 ????4 ????1 ????- ? ????- ????- ????- ? ? ????- ????- ? ? ? ????44 ????28 ????3 ????12 ????- ????6 ????7 ????- ? ????- ????- ????- ? ? ????- ????- ? ? ? ????39 ????16 ????11 ????15 ????1 ????5 ????1 ????1 ? ????- ????- ????- ? ? ????- ????14 ? ? ? ????42 ????19 ????11 ????11 ????1 ????4 ????1 ????- ? ????- ????- ????- ? ? ????- ????11 ? ? ? ????- ????7 ????- ????22 ????- ????- ????- ????- ? ????- ????- ????66 ? ? ????5 ????- ?
Thermal expansivity (* 10 -7/℃) ????70.0 ????69.3 ????72.2 ????74.6 ????75.0 ????80.0 ????83.0 ????81.5 ????80.0
Softening temperature (℃) ????553 ????557 ????556 ????554 ????550 ????555 ????557 ????555 ????560
Table 2
??a ??????b ?????c ???d ????e
The stopping composition kind Mullite Mullite Mullite Aluminum oxide Silica
?d50(μm) ??1.5 ??????3 ?????9 ???3 ????1.5
Then, use the glass powder of table 1 and the stopping composition powder modulation next door material of table 2.
At first, in the mode of the cooperation ratio shown in table 3~5, mix each glass powder and various ceramic stopping composition powder.In addition, the cooperation ratio shown in the table is represented with weight %.Then, the terpinol solution of mixing mixture that obtains and ethyl cellulose is used mashed prod to form as the next door.
Use this mashed prod, estimate shape maintains, transmitance, thickness.And, use the mixed powder that constitutes by glass powder and stopping composition powder, estimate specific inductivity.It is as shown in the table for the result.
In addition, as following, estimate shape maintains.At first, prepare two windows with sheet glass (thickness of slab is 1.7mm), utilizing silk screen print method to form thickness on each sheet glass is the overlay of 200 μ m.Then, press dry dry thin protective film (DFR) on the overlay upper strata.Then, as mask, utilize the method for sandblasting to remove the part that protective membrane of no use covers this protective membrane, form the shape in next door.Then, at the softening temperature of glass powder and on the other hand under, burnt till respectively 10 minutes on the one hand than the high 20 ℃ temperature of the softening temperature of glass powder.Estimate the height, H (softening temperature), H (softening temperature+20 ℃) in the next door of two kinds that form like this, utilize following such calculating formula to obtain its velocity of variation Δ H, estimate the shape maintains of next door material.In addition, the height in next door utilizes SEM (scanning electron microscope) to observe the cross section in next door and is tried to achieve by its photo.
Δ H=(H (softening temperature+20 ℃))/(H (softening temperature)) * 100
Then, as following, estimate transmitance and thickness.At first, use and above-mentioned same method, burning till the mode that thickness is 30 ± 1 μ m, go up the overlay that forms about 50 μ m with sheet glass (thickness of slab 1.7mm),, make and burn till film by under the temperature of the softening temperature of glass powder, burning till 10 minutes at window.To the next door of making like this, be determined at the diffusion transmitance of 550nm.And, this value is scaled thickness 30 μ m, be recorded as transmitance.In addition, the mensuration of diffusion transmitance is carried out with island Tianjin system spectrophotometer UV-3100 and under the detector of subsidiary integrating sphere, measures the value that enters glass substrate.Moreover the thickness of each test portion is a value of estimating the thickness after burning till, measures with milscale.
Then, with regard to specific inductivity, be squeezed into the blended powder discoid with metal metal die, after burning till under 560 ℃, grind to form the thickness of 2mm and be made into the disk test portion, then, form the Ag electrode on the two sides, be determined at the value that cycle is 1MHz with Yokogawa ヒ ユ one レ Star ト パ Star カ one De Co., Ltd. system LCR instrument.
Table 3
????1 ????2 ????3 ????4 ????5 ????6 ????7
Glass powder Kind ????A ????A ????A ????B ????B ????B ????B
Amount ????78 ????80 ????80 ????80 ????83 ????80 ????75
The stopping composition powder Kind ????a ????a ????a ????a ????b ????a ????b
Amount ????17 ????20 ????17 ????20 ????17 ????14 ????18
Kind ????b ????d ????d ????e
Amount ????5 ????3 ????6 ????7
Firing temperature (℃) ????560 ????560 ????560 ????560 ????560 ????560 ????560
Thermal expansivity (* 10 -7/℃) ????65 ????66 ????67 ????65 ????68 ????68 ????70
Shape maintains, Δ H (%) ????93 ????90 ????92 ????92 ????89 ????92 ????94
Transmitance (%.at550nm) ????60 ????62 ????59 ????62 ????63 ????55 ????57
Thickness (μ m) ????30 ????30 ????29 ????29 ????30 ????30 ????31
Specific inductivity ????8.1 ????8.2 ????8.3 ????8.2 ????8.2 ????8.4 ????7.6
Table 4
????8 ????9 ????10 ????11 ????12 ????13 ????14
Glass powder Kind ????C ????C ????D ????D ????E ????E ????E
Amount ????83 ????81 ????72 ????76 ????80 ????74 ????79
The stopping composition powder Kind ????a ????b ????a ????a ????a ????b ????a
Amount ????17 ????17 ????15 ????20 ????20 ????19 ????10
Kind ????e ????b ????e ????e ????b
Amount ????2 ????13 ????4 ????7 ????11
Firing temperature (℃) ????560 ????560 ????560 ????560 ????560 ????560 ????560
Thermal expansivity (* 10 -7/℃) ????68 ????71 ????69 ????72 ????69 ????72 ????68
Shape maintains, Δ H (%) ????90 ????91 ????93 ????92 ????93 ????94 ????92
Transmitance (%.at550nm) ????61 ????61 ????60 ????58 ????62 ????61 ????62
Thickness (μ m) ????31 ????31 ????30 ????30 ????31 ????30 ????30
Specific inductivity ????8.2 ????8.1 ????8.0 ????7.8 ????8.2 ????7.6 ????8.1
Table 5
????15 ????16 ????17 ???18 ????19 ????20 ????21 ????22 ????23 ????24
Glass powder Kind ????A ????A ????A ???D ????E ????E ????G ????H ????H ????I
Amount ????80 ????90 ????78 ???55 ????78 ????77 ????80 ????81 ????79 ????80
The stopping composition powder Kind ????c ????a ????a ???b ????a ????a ????a ????a ????a ????d
Amount ????20 ????10 ????3 ???35 ????10 ????8 ????14 ????17 ????14 ????20
Kind ????d ???d ????d ????d ????d ????e ????d
Amount ????19 ???10 ????12 ????15 ????6 ????2 ????7
Firing temperature (℃) ????560 ????560 ????560 ???560 ????560 ????560 ????560 ????560 ????560 ????560
Thermal expansivity (* 10 -7/℃) ????66 ????70 ????72 ???67 ????70 ????72 ????74 ????74 ????73 ????78
Shape maintains, Δ H (%) ????83 ????82 ????91 ???94 ????91 ????92 ????90 ????91 ????92 ????93
Transmitance (%.at550nm) ????59 ????66 ????48 ???47 ????62 ????58 ????62 ????64 ????61 ????61
Thickness (μ m) ????31 ????30 ????31 ???30 ????30 ????31 ????31 ????30 ????30 ????30
Specific inductivity ????8.8 ????8.4 ????8.7 ???7.9 ????8.4 ????8.6 ????8.6 ????8.4 ????8.5 ????11.3

Claims (15)

1. a plasma display panel forms material with the next door, it is characterized in that,
Comprise ZnO-B 2O 3Glass frit end 60~90 quality % and stopping composition powder 10~40 quality %, mullite powders accounts for 20~100 quality % of described stopping composition powder.
2. plasma display panel as claimed in claim 1 forms material with the next door, it is characterized in that, described mullite powders accounts for 30~100 quality % of described stopping composition powder.
3. plasma display panel as claimed in claim 1 forms material with the next door, it is characterized in that described ZnO-B 2O 3The glass frit end is 60~85 quality %, and described stopping composition powder is 15~40 quality %.
4. plasma display panel as claimed in claim 1 forms material with the next door, it is characterized in that, 50% median size of described mullite powders is 0.5~6 μ m.
5. plasma display panel as claimed in claim 1 forms material with the next door, it is characterized in that described ZnO-B 2O 3The glass frit end is made of the glass that contains the ZnO more than the 30 quality %.
6. plasma display panel as claimed in claim 1 forms material with the next door, it is characterized in that described ZnO-B 2O 3The glass frit end is by the B that contains more than the 15 quality % 2O 3Glass constitute.
7. plasma display panel as claimed in claim 1 forms material with the next door, it is characterized in that ZnO-B 2O 3The glass frit end constitutes by containing the glass that BaO and content is no more than 25 quality %.
8. plasma display panel as claimed in claim 1 forms material with the next door, it is characterized in that described ZnO-B 2O 3The glass frit end is by ZnO-B 2O 3System lead-free glass constitutes.
9. plasma display panel as claimed in claim 1 forms material with the next door, it is characterized in that described ZnO-B 2O 3The glass frit end, in Quality Percentage, ZnO is 30~60% by containing, B 2O 3Be 15~35%, BaO is 0~25%, SiO 2Be 3~20%, Li 2O is 0.2~6%, Li 2O+Na 2O+K 2O is 1~12% glass formation.
10. a plasma display panel next door forms and uses mashed prod, it is characterized in that, the next door of containing claim 1~9 forms material.
Use the embryo sheet 11. a plasma display panel next door forms, it is characterized in that, the next door of containing claim 1~9 forms material.
12. the next door of a plasma display panel is characterized in that, the next door of use claim 1~9 forms material and forms.
13. the next door of a plasma display panel is characterized in that, uses the next door formation of claim 10 to form with mashed prod.
14. the next door of a plasma display panel is characterized in that, uses the next door formation of claim 11 to form with the embryo sheet.
15. the next door of each described plasma display panel of claim 12~14 is characterized in that, the diffusion transmitance value that is scaled the 550nm of thickness 30 μ m is counted more than 50% with the transmitance value that enters glass substrate.
CNB2005100569259A 2004-03-23 2005-03-23 Plasma display forms material with the next door Expired - Fee Related CN100569684C (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2004084004 2004-03-23
JP2004084004 2004-03-23
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JP2004118206 2004-04-13

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101456674B (en) * 2009-01-04 2011-05-11 武汉理工大学 Rare-earth doped leadless and low-melting point sealing glass and its preparation method
CN102623283A (en) * 2011-02-01 2012-08-01 飞诺迪显示电子有限公司 Glass composition for photosensitive barrier of display device

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08301631A (en) * 1995-03-07 1996-11-19 Asahi Glass Co Ltd Plasma display panel
JP2000095544A (en) * 1998-07-22 2000-04-04 Mitsubishi Materials Corp Glass composition, paste using the same, insulator, partition wall for fpd and insulating layer
KR100395594B1 (en) * 2000-12-29 2003-08-21 엘지마이크론 주식회사 Dielectric material for rear panel of plasma display panel
JP2002274884A (en) 2001-01-09 2002-09-25 Mitsubishi Materials Corp Paste for forming ceramic rib and method of manufacturing for the same as well as method of forming rib-like object using the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101456674B (en) * 2009-01-04 2011-05-11 武汉理工大学 Rare-earth doped leadless and low-melting point sealing glass and its preparation method
CN102623283A (en) * 2011-02-01 2012-08-01 飞诺迪显示电子有限公司 Glass composition for photosensitive barrier of display device

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KR20060043860A (en) 2006-05-15
CN100569684C (en) 2009-12-16
KR101141092B1 (en) 2012-05-03

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