WO2000076273A1 - Corps de chauffe en ceramique et procede de fabrication, et pate conductrice pour element chauffant - Google Patents
Corps de chauffe en ceramique et procede de fabrication, et pate conductrice pour element chauffant Download PDFInfo
- Publication number
- WO2000076273A1 WO2000076273A1 PCT/JP1999/003086 JP9903086W WO0076273A1 WO 2000076273 A1 WO2000076273 A1 WO 2000076273A1 JP 9903086 W JP9903086 W JP 9903086W WO 0076273 A1 WO0076273 A1 WO 0076273A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- heating element
- ceramic
- conductive paste
- metal
- oxide
- Prior art date
Links
- 238000010438 heat treatment Methods 0.000 title claims abstract description 204
- 239000000919 ceramic Substances 0.000 title claims abstract description 197
- 238000004519 manufacturing process Methods 0.000 title claims description 15
- 239000000758 substrate Substances 0.000 claims abstract description 97
- 239000002923 metal particle Substances 0.000 claims abstract description 63
- 150000004767 nitrides Chemical class 0.000 claims abstract description 37
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 31
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 31
- 238000005245 sintering Methods 0.000 claims abstract description 18
- 239000002245 particle Substances 0.000 claims description 32
- 239000010410 layer Substances 0.000 claims description 31
- 238000000034 method Methods 0.000 claims description 30
- 229910052751 metal Inorganic materials 0.000 claims description 28
- 239000002184 metal Substances 0.000 claims description 28
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 24
- 239000000843 powder Substances 0.000 claims description 20
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 17
- 238000007639 printing Methods 0.000 claims description 17
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 17
- 239000010937 tungsten Substances 0.000 claims description 17
- 229910052721 tungsten Inorganic materials 0.000 claims description 17
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 13
- 239000011133 lead Substances 0.000 claims description 13
- 229910052750 molybdenum Inorganic materials 0.000 claims description 13
- 239000011733 molybdenum Substances 0.000 claims description 13
- 229910052759 nickel Inorganic materials 0.000 claims description 12
- 229910000464 lead oxide Inorganic materials 0.000 claims description 9
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 claims description 9
- 239000011787 zinc oxide Substances 0.000 claims description 9
- 229910052810 boron oxide Inorganic materials 0.000 claims description 8
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims description 8
- SIWVEOZUMHYXCS-UHFFFAOYSA-N oxo(oxoyttriooxy)yttrium Chemical compound O=[Y]O[Y]=O SIWVEOZUMHYXCS-UHFFFAOYSA-N 0.000 claims description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 5
- 238000010030 laminating Methods 0.000 claims description 5
- 230000001590 oxidative effect Effects 0.000 claims description 5
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 5
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 5
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 5
- 239000011247 coating layer Substances 0.000 claims description 4
- 229910000510 noble metal Inorganic materials 0.000 claims description 4
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 claims description 4
- QIJNJJZPYXGIQM-UHFFFAOYSA-N 1lambda4,2lambda4-dimolybdacyclopropa-1,2,3-triene Chemical compound [Mo]=C=[Mo] QIJNJJZPYXGIQM-UHFFFAOYSA-N 0.000 claims description 3
- 229910039444 MoC Inorganic materials 0.000 claims description 3
- 238000007747 plating Methods 0.000 claims description 3
- 238000003825 pressing Methods 0.000 claims description 3
- 238000000465 moulding Methods 0.000 claims description 2
- 239000004020 conductor Substances 0.000 claims 1
- 238000002156 mixing Methods 0.000 abstract description 8
- 229910000679 solder Inorganic materials 0.000 description 16
- 235000012431 wafers Nutrition 0.000 description 14
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 13
- 239000002904 solvent Substances 0.000 description 13
- 239000004065 semiconductor Substances 0.000 description 12
- 229910052709 silver Inorganic materials 0.000 description 12
- 239000004332 silver Substances 0.000 description 12
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 10
- 238000009826 distribution Methods 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 229920005822 acrylic binder Polymers 0.000 description 8
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- 238000007650 screen-printing Methods 0.000 description 6
- 229910052710 silicon Inorganic materials 0.000 description 6
- 239000010703 silicon Substances 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 229910000833 kovar Inorganic materials 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229910052763 palladium Inorganic materials 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 229910010271 silicon carbide Inorganic materials 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 229910052582 BN Inorganic materials 0.000 description 3
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 3
- 229910052737 gold Inorganic materials 0.000 description 3
- 239000010931 gold Substances 0.000 description 3
- 230000020169 heat generation Effects 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- RUDFQVOCFDJEEF-UHFFFAOYSA-N yttrium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Y+3].[Y+3] RUDFQVOCFDJEEF-UHFFFAOYSA-N 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000001856 Ethyl cellulose Substances 0.000 description 2
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- KZVBXDYTYQEHEW-UHFFFAOYSA-N [Pb].[Pb].[Ag] Chemical compound [Pb].[Pb].[Ag] KZVBXDYTYQEHEW-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000007772 electroless plating Methods 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 229920001249 ethyl cellulose Polymers 0.000 description 2
- 235000019325 ethyl cellulose Nutrition 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- LWUVWAREOOAHDW-UHFFFAOYSA-N lead silver Chemical compound [Ag].[Pb] LWUVWAREOOAHDW-UHFFFAOYSA-N 0.000 description 2
- 150000001247 metal acetylides Chemical class 0.000 description 2
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 2
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- 235000017281 sodium acetate Nutrition 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- KWSLGOVYXMQPPX-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-2h-tetrazole Chemical compound FC(F)(F)C1=CC=CC(C2=NNN=N2)=C1 KWSLGOVYXMQPPX-UHFFFAOYSA-N 0.000 description 1
- 229910001020 Au alloy Inorganic materials 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
- -1 acryl Chemical group 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000007606 doctor blade method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- LQBJWKCYZGMFEV-UHFFFAOYSA-N lead tin Chemical compound [Sn].[Pb] LQBJWKCYZGMFEV-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- NFFIWVVINABMKP-UHFFFAOYSA-N methylidynetantalum Chemical compound [Ta]#C NFFIWVVINABMKP-UHFFFAOYSA-N 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 229910001120 nichrome Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 239000003870 refractory metal Substances 0.000 description 1
- 230000004043 responsiveness Effects 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 229910003468 tantalcarbide Inorganic materials 0.000 description 1
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B3/00—Ohmic-resistance heating
- H05B3/20—Heating elements having extended surface area substantially in a two-dimensional plane, e.g. plate-heater
- H05B3/22—Heating elements having extended surface area substantially in a two-dimensional plane, e.g. plate-heater non-flexible
- H05B3/28—Heating elements having extended surface area substantially in a two-dimensional plane, e.g. plate-heater non-flexible heating conductor embedded in insulating material
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B3/00—Ohmic-resistance heating
- H05B3/10—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor
- H05B3/12—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor characterised by the composition or nature of the conductive material
- H05B3/14—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor characterised by the composition or nature of the conductive material the material being non-metallic
- H05B3/141—Conductive ceramics, e.g. metal oxides, metal carbides, barium titanate, ferrites, zirconia, vitrous compounds
- H05B3/143—Conductive ceramics, e.g. metal oxides, metal carbides, barium titanate, ferrites, zirconia, vitrous compounds applied to semiconductors, e.g. wafers heating
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/67—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere
- H01L21/67005—Apparatus not specifically provided for elsewhere
- H01L21/67011—Apparatus for manufacture or treatment
- H01L21/67098—Apparatus for thermal treatment
- H01L21/67103—Apparatus for thermal treatment mainly by conduction
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B3/00—Ohmic-resistance heating
- H05B3/10—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor
- H05B3/12—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor characterised by the composition or nature of the conductive material
Definitions
- the present invention relates to a ceramic heater for drying mainly used in the semiconductor industry, and more particularly to a thin and light ceramic heater which is easy to control the temperature, a method of manufacturing the same, and a heating element of the heater.
- the present invention relates to a conductive paste used for forming a conductive paste.
- Typical semiconductor products are manufactured, for example, by applying an etching resist (photosensitive resin) on a silicon wafer and then etching.
- the photosensitive resin applied to the silicon wafer surface must be dried after application.
- a drying method it is general to place a silicon wafer coated with the resin on a heater and heat it.
- a typical example of such a heater is a heater in which a heating element is attached to the back surface of an aluminum substrate.
- a metal heater has the following problems.
- the substrate as the heater body is made of metal, the thickness must be increased to about 15 mm. This is because, in a thin metal plate, warpage and distortion occur due to thermal expansion caused by heating, and the wafer placed on the metal plate is damaged or tilted. Therefore, the conventional metal heater has a problem that it is heavy and bulky.
- Heating of the silicon wafer by the heater is performed by controlling the temperature of the substrate by adjusting the voltage and current applied to the heating element.
- the temperature of the heater substrate is not affected by changes in voltage or current. There was a problem that it did not follow quickly and had poor temperature control characteristics.
- a main object of the present invention is to provide a thin and light heater which can be easily controlled in temperature and a method for manufacturing the same.
- Another object of the present invention is to provide a conductive paste for a heating element having excellent heat generation characteristics. Disclosure of the invention
- a ceramic having excellent thermal conductivity particularly a nitride ceramic or a carbide ceramic, is used as a substrate for a heater instead of a metal such as aluminum.
- C Such ceramic substrates do not warp or warp even if they are thin, and they can control the temperature quickly and easily, especially when controlling the temperature by changing the voltage or current applied to the heating element. was found to be excellent in responsiveness.
- a conductive paste containing metal particles generally has a property of being difficult to adhere to nitride ceramics and carbide ceramics. We have learned that the adhesion is improved through sintering.
- the gist configuration of the present invention developed based on such knowledge is as follows.
- the present invention is a ceramic heater in which a heating element is provided on a surface of a ceramic substrate made of a nitride ceramic or a carbide ceramic.
- the heating element is disposed so as to be partially embedded in the ceramic substrate.
- the heating element is preferably made of a sintered body of metal particles.
- the heating element comprises metal particles and at least one metal oxide selected from lead oxide, zinc oxide, silicon oxide, boron oxide, aluminum oxide, yttrium oxide and titanium oxide. Is preferred.
- the metal particles are noble metal, lead, tungsten, molybdenum and nickel It is preferable to use at least one kind selected from the following.
- the surface of the heating element is preferably covered with a non-oxidizing metal layer.
- the heating element has a sectional shape having a sectional area ratio (width of the heating element Z and thickness of the heating element) of 10 to 10,000 force.
- the cross-sectional aspect ratio (the width of the heating element, the thickness of the heating element) is from 1 to 100 mm.
- a flat heating element is provided inside the ceramic substrate made of the nitride ceramic or the carbide ceramic.
- a flat heating element is disposed inside a ceramic substrate made of a nitride ceramic or a carbide ceramic, and the position of the heating element is set in the thickness direction from the center of the substrate.
- a ceramic heater characterized in that it is disposed at an eccentric position, and a surface farther from the heating element is a heating surface.
- This heater also preferably has a heating element having the above-mentioned configuration of 2 to 8.
- the heating element is preferably made of a sintered body of metal particles or conductive ceramics.
- the heating element is preferably tungsten, molybdenum, tungsten carbide, or molybdenum carbide.
- the degree of eccentricity of the heating element is preferably more than 50% from the heated surface of the substrate and less than 100%.
- the cross-sectional height ratio (width of the heating element / thickness of the heating element) of the heating element is preferably 10 to 10,000.
- the present invention also proposes a method for manufacturing a ceramic heater, characterized by including at least the following steps (1) to (3).
- the conductive paste used in the step (2) it is preferable to use a paste of a mixture of metal particles and a metal oxide.
- the present invention also proposes a method for manufacturing a ceramic heater characterized by including at least the following steps (1) to (4).
- step (3) A step of laminating one or more sheets of the conductive paste-printed green sheet and another green sheet obtained by performing the same treatment as in step (1).
- step 18 When laminating the green sheet obtained by the same processing as in step 1 on the upper and lower sides of the green sheet printed with the conductive base obtained in step 2, the upper and lower sides It is preferable to adjust the ratio of the number of green sheets in the range of 1Z1 to 1Z99.
- the present invention also proposes a conductive paste for a ceramic heater and a heating element comprising metal particles and a metal oxide.
- metal particles it is preferable to use a noble metal or one or more selected from the group consisting of lead, tungsten, molybdenum and nickel.
- the metal oxide may be one or more selected from the group consisting of lead oxide, zinc oxide, silicon oxide, boron oxide, aluminum oxide, yttrium oxide, and titanium oxide. preferable.
- the conductive paste is more than 0.1 wt% to less than 1 Qwt% with respect to the metal particles. It is preferable to use a paste obtained by mixing a metal oxide.
- the metal particles preferably have an average particle size of 0.1 to 1.0 ⁇ im.
- the metal particles are preferably flaky particles or a mixture of spherical particles and flaky particles.
- FIG. 1 is a plan view of one ceramic heater of the present invention
- FIG. 2 is a cross-sectional view showing a state of use of the ceramic heater of the present invention
- FIG. 3 is a diagram for explaining a method of manufacturing a ceramic heater of the present invention
- FIG. 4 is a diagram showing terminal pins in through-holes.
- FIG. 5 is an explanatory view showing another example of manufacturing the ceramic heater of the present invention
- FIG. 6 is an explanatory view showing still another example of manufacturing the ceramic heater of the present invention. I can do it.
- the ceramic heater of the present invention uses a ceramic substrate made of insulating nitride ceramic or carbide ceramic, and forms a heat generating body on one surface of the ceramic substrate by printing. It has a heating surface on which semiconductor products such as silicon wafers are placed and heated.
- the ceramic heater of the present invention may also be one in which a heating element having a flat cross-sectional shape is disposed (sandwiched) inside the ceramic substrate.
- the heating element is located at the center of the substrate. May be disposed eccentrically in the thickness direction, and the surface remote from the heating element may be a heating surface.
- the nitride ceramic or carbide ceramic constituting the above substrate has a characteristic that it has a smaller thermal expansion coefficient than metal and does not warp or be distorted by heating even if it is thin. Therefore, the substrate of one heater can be made thin and light.
- such a ceramic substrate has a high thermal conductivity and is thin, so that the surface temperature of the substrate quickly follows a temperature change of the heating element. That is, when the temperature of the heating element is changed by changing the electric power and the electric current, the surface temperature of the ceramic substrate quickly changes following the change.
- the ceramic heater according to the present invention has a heating surface on the side opposite to the side on which the heating element is provided, or is far from a flat heating element which is arranged eccentrically in the thickness direction from the center of the substrate.
- U.S. Pat. No. 5,656,824 does not decenter the heating element and does not disclose a specific shape such as an aspect ratio. For this reason, the temperature uniformity of the heated surface is poor.
- the ceramic substrate preferably has a thickness of about 0.5 to 5 mm. The reason is that if it is too thin, it will be easily broken.
- the nitride ceramic as a material of such a ceramic substrate is selected from metal nitride ceramics, for example, any one selected from aluminum nitride, silicon nitride, boron nitride, boron nitride, titanium nitride, and the like. It is desirable to use one or more.
- the carbide ceramic is selected from metal carbide ceramics, for example, silicon carbide, zirconia, titanium carbide, tantalum carbide, tungsten carbide and the like, and it is desirable to use at least one of them.
- aluminum nitride is preferred. This is because aluminum nitride has the highest thermal conductivity of 180 W / m ⁇ K.
- the heating element disposed on the ceramic substrate is formed by sintering metal particles or metal oxide particles in the conductive paste. This is because each of the particles can be baked on the surface of the ceramic substrate by heating and baking. The sintering treatment is performed to such an extent that the metal particles or the metal particles and the ceramic are fused to each other.
- the thickness of the patterned heating element 2 is desirably about 1 to 50, but when the heating element 2 is formed on the surface of the substrate 1, the thickness is preferably 1 to 10 Aim. On the other hand, when the heating element 2 is formed inside the substrate 1, the thickness is preferably 1 to 50 ⁇ m.
- the width of the heating element is preferably about 0.1 to 20 mm, but when the heating element 2 is formed on the surface of the substrate 1, the width is 0.1 to 5 mm.
- the thickness is preferably about 1 to 20 mm. The reason for limiting to these ranges is generally that the resistance can be changed by changing the thickness and width of the heating element 2, but the above range is most effective for controlling the temperature of the heating element. is there. Note that the resistance value of the heating element 2 increases as it becomes thinner and thinner. It will be good.
- both the thickness and the width can be increased.
- the distance between the heating surface and the heating element becomes short, and the temperature uniformity of the heating surface of the ceramic substrate 1 is reduced, so that the heating surface is uniformly heated. Therefore, it is necessary to increase the width of the heating element 2 itself.
- a heating element is provided inside, there is no need to consider the adhesion of the substrate to nitride ceramics, etc., so it is necessary to use refractory metals such as tungsten and molybdenum, and carbides such as tungsten and molybdenum. It is possible to increase the resistance value. As a result, the thickness of the heating element can be increased for the purpose of preventing disconnection and the like.
- This heating element generally has a rectangular or elliptical cross section, and preferably has a flat shape.
- the heating element when a heating element is provided inside the ceramic substrate 1, the heating element must be flat. The reason for this is that a flat cross section is more likely to radiate heat toward the heating surface, so that it is difficult to generate a temperature distribution on the heating surface.
- the end-to-side ratio (width of the heating element Z and thickness of the heating element) of the cross section of the heating element 2 is desirably about 10 to 10000, and preferably 50 to 5000. By adjusting within this range, the resistance value of the heating element 2 can be increased, and at the same time, the uniformity of the temperature distribution on the heating surface can be ensured.
- the heat transfer amount in the direction of the heating surface of the substrate decreases when the heat-sink ratio is small.
- the heating surface has the same heat distribution as the heating element pattern.
- the aspect ratio is too large, the temperature just above the center of the heating element pattern will be high, and eventually, a heat distribution similar to that of the heating element pattern will be formed on the heating surface.
- the aspect ratio the width of the heating element Z and the thickness of the heating element
- the cross section of the heating element 2 be in the range of 10 to 100 mm ().
- the heating element 2 When the heating element 2 is formed inside the ceramic substrate 1, the end-to-side ratio can be increased. However, when the heating element 2 is provided inside, the heating surface and the heat generation Since the distance to the body becomes shorter and the temperature uniformity on the surface decreases, the heating element itself needs to be flat.
- the position of the heating element in the thickness direction can be eccentrically arranged. It is desirable to set the degree of the position from one surface (heating surface) of the substrate to more than 50% to less than 10%. The reason is that the temperature distribution on the heating surface can be prevented, and the warpage of the ceramic substrate can be suppressed. Preferably it is 55-95%.
- the heating element 2 When the heating element 2 is formed inside the ceramic substrate 1, the heating element may be divided into a plurality of layers. In this case, it is desirable that the patterns of the respective layers are formed so as to complement each other, and that a complete pattern is formed in any layer when viewed from the heating surface. For example, a structure in which the upper layer and the lower layer are arranged in a zigzag pattern with each other so as to form a complete pattern as a whole.
- the heating element 2 When the heating element 2 is disposed on the surface of the ceramic substrate 1, it is desirable that a part (bottom) of the heating element be disposed in a state buried in the ceramic substrate. This is because, by disposing the heating element in this way, it is possible to simultaneously improve the resistance control of the heating element and the adhesion to the ceramic base material.
- the conductive paste is generally a mixture of a resin, a solvent, a thickener, and the like, in addition to metal particles for ensuring conductivity, or conductive ceramic.
- precious metal gold, silver, platinum, palladium
- lead tungsten emissions
- molybdenum c these metals more than any one selected from nickel is used rather relatively oxidized difficulty, Because it shows sufficient resistance to generate heat c
- the conductive ceramic any one or more selected from carbides of tungsten / molybdenum and the like can be used.
- These metal particles or conductive ceramics preferably have a particle size of Q. 1 to 10 m. If it is too fine, it is easily oxidized, while if it is too large, it becomes difficult to sinter and the resistance value becomes large.
- the metal particles may be spherical, scaly, or a mixture of spherical and scaly.
- a metal oxide described later is easily held between the metal particles, and the adhesion between the heating element and the nitride ceramic or the like is improved.
- a resin used for such a conductive paste an epoxy resin, a phenol resin, and the like are preferable.
- Isopropyl alcohol and the like can be used as the solvent.
- Cellulose and the like can be used as the thickener.
- the conductive paste further contains a metal oxide in addition to the metal particles so that the heating element is a sintered body of a mixture of the metal particles and the metal oxide. That is, if a metal oxide is interposed between the nitride ceramic or the carbide ceramic and the metal particles, the adhesion between them can be improved. Although the reason why the adhesion is improved is not clear, the surface of the metal particles and the surface of the nitride ceramic or the surface of the carbide ceramic slightly contain an oxide film. It is presumed that the metal particles and the nitride ceramic or the carbide ceramic adhere to each other via the oxide as a result of showing an affinity for the material and easily integrating them.
- the metal oxide at least one selected from the group consisting of lead oxide, zinc oxide, silicon oxide, boron oxide, aluminum oxide, yttrium oxide, and titanium oxide is used. This is because these oxides can improve the adhesion between the metal particles and the nitride ceramic or the carbide ceramic without increasing the resistance value of the heating element.
- the addition amount of the metal oxide is 0.1 to less than 10 wt% with respect to the metal particles. It is desirable. The reason for this is that if the content is less than 0.1 wt%, the effect of the addition is ineffective, whereas if it is 1 Owt% or more, the resistance value of the heating element 2 becomes too large.
- the mixing ratio of these metal oxides is 1 to 1 Owt% for lead oxide and 1 to 30 t% for silicon oxide and 5 to 30 t% for boron oxide when the total amount of metal oxides is 100 wt%.
- Aluminum oxide 1-1 ⁇ 1 wt%, yttrium oxide 1 ⁇ 50 wt%, titanium oxide 1 ⁇ 50 wt% It is desirable that the total be adjusted so that the total does not exceed 10 Owt%. These ranges are particularly effective in improving the adhesion between the metal particles and the nitride ceramic.
- the sheet resistivity of the heating element can be set to 1 to 45 ⁇ . If the sheet resistivity is too large, the amount of heat generated becomes too large with respect to the applied voltage, and in the case where a heating element is provided on the surface of the ceramic substrate, control becomes difficult. When the amount of the metal oxide is 1 [] wt% or more, the sheet resistivity exceeds 5 ⁇ ⁇ , and the heat generation becomes too large to control the temperature. Uniformity decreases.
- the area resistivity was 5 Although it has been considered that it is unsuitable as a heater resistor (Japanese Patent Application Laid-Open No. 4300249), the present invention conversely sets the area resistivity to 45 mQZL or less to control the temperature. The temperature distribution was made uniform to ensure uniformity.
- the heating element is a sintered body of metal particles, if the heating element is exposed to the air, it is easily oxidized and the resistance value changes. Therefore, oxidation was prevented by coating the surface of the sintered metal particles with a metal layer.
- the thickness of the metal layer is preferably about 0.1 to 1. This is because the heating element can be prevented from oxidizing without changing the resistance value of the heating element.
- the metal coated on the surface of the metal particle sintered body may be a non-oxidizing metal.
- a non-oxidizing metal For example, at least one selected from gold, silver, palladium, platinum, and nickel is preferable. Of these, nickel is preferred.
- the heating element generally needs a terminal to connect to the power supply, and this terminal is attached to the heating element via solder, but so-called nickel also has the function of preventing heat diffusion of the solder. From one. Kovar terminal pins can be used as the connection terminals.
- the heating element when the heating element is arranged inside the ceramic substrate, the heating element surface is not oxidized, so no coating is required.
- the solder may be a solder alloy such as silver lead, lead tin, bismuth soot, etc., and the thickness of the solder layer is 0.1 to 50 ⁇ m, which is a sufficient range to secure the connection by the solder. It is.
- thermocouple G1 can be embedded in the ceramic substrate 1 as necessary, as shown in FIG. 5 (d).
- the temperature of the ceramic substrate 1 is measured by the thermocouple 61, the voltage and current are adjusted based on the data, and the temperature of the heating surface of the ceramic substrate 1 can be easily and accurately controlled.
- FIG. 2 is a partial cross-sectional view showing a usage state of the ceramic heater of the present invention.
- reference numeral 3 denotes a terminal pin
- 4 denotes a sintered body of metal (Ag—Pb) particles
- 5 denotes a metal (N i) coating layer.
- Reference numeral 6 denotes a solder layer through which the terminal pins 3 are mounted.
- a plurality of through-holes 8 are provided in the ceramic substrate 1, and support pins 7 of a semiconductor wafer are inserted into the through-holes 8.
- Mount 9 adjacent or with a slight gap In this case, when the semiconductor wafer 9 is delivered to a carrier (not shown) or the semiconductor wafer 19 is received from the carrier, the support pins 7 are moved up and down.
- a heating element is formed on the surface of a ceramic substrate (Fig. 2)
- powder of a nitride ceramic such as nitrided nitride or a powder of a carbide ceramic such as silicon carbide, and, if necessary, a sintering aid such as an iterator.
- the mixed powder composed of the binder is made into granules by a method such as a spray-drying method, and the obtained granules are put into a mold or the like and pressed to be formed into a plate shape to form a formed body.
- the above-mentioned formed body is provided with a through hole 8 for inserting a support pin 7 of a semiconductor wafer and a concave portion G2 for burying a thermocouple 61 as necessary.
- the green compact is heated and fired and sintered to produce a ceramic plate.
- a ceramic substrate for a heater without pores is manufactured by applying pressure.
- the heating and sintering may be performed at a temperature equal to or higher than the sintering temperature.
- the temperature is preferably 100 to 250 ° C.
- a conductive paste containing metal particles is printed on the surface of the ceramic plate (one heater, ie, ceramic substrate) obtained in the above step (1) to form a metal particle layer 4. Forming step.
- a conductive paste having high viscosity and fluidity composed of metal particles, a resin, and a solvent is printed at a required position by a method such as screen printing.
- the reason why the conductive paste is applied by printing to form the metal particle layer 4 is that, in order to form the heating element 2 for heating the entire ceramic substrate to a uniform temperature, a concentric circle as shown in Fig. 1 is used. This is because it is desirable to accurately form a pattern in which the heating element is formed. Further, it is preferable that the cross-sectional shape of the heating element is a flat cross-sectional shape based on a square.
- heating and sintering temperature is 500 to 1000 ° C.
- a metal oxide is added to the conductive paste, the metal particles, the ceramic plate and the metal oxide are sintered and integrated, so that the heating element and The adhesion to the ceramic plate is improved.
- a metal coating layer 5 may be formed on the surface of the metal particle layer 4. This treatment can be performed by electroplating, electroless plating, or sputtering. However, considering mass production, electroless plating is optimal.
- terminal pins 3 for connection to a power supply are attached by soldering.
- a green sheet 31 is obtained by mixing a ceramic powder such as a nitride ceramic or a carbide ceramic with a binder and a solvent.
- the above-mentioned ceramic powder aluminum nitride, silicon carbide and the like can be used, and if necessary, a sintering aid such as yttrium oxide (ittrium) is added. Is also good.
- the binder is preferably at least one selected from the group consisting of acrylic binder, ethyl cellulose, butyl cellulose, and polyvinylalte.
- the solvent is selected from terpione and glycol, and it is preferable to use at least one of them.
- a paste obtained by mixing these is formed into a sheet by a doctor blade method to produce a green sheet 31.
- the obtained green sheet may be provided with a through hole 8 for inserting a support pin 7 of a silicon wafer and a concave portion 62 for embedding a thermocouple 61 as necessary.
- the through hole 8 and the concave portion 62 are formed by one method such as punching.
- the thickness of the green sheet is preferably about 0.1 to 5 mm.
- the metal particle layer 4 serving as a heating element is formed by printing a conductive paste using a metal paste or a conductive ceramic.
- These pastes contain metal particles or conductive ceramic particles, such as tungsten or molybdenum, and tungsten or molybdenum carbide as the conductive ceramic particles. is there. This is because they are not easily oxidized and the decrease in thermal conductivity is small.
- the average particle diameter of the above-mentioned tungsten particles or molybdenum particles is preferably [] .1 to 5 / m, because printing the conductive paste becomes difficult if the particles are too large or too small.
- the paste 85 to 97 parts by weight of metal particles or conductive ceramic particles, at least one kind of binder selected from acryl-based, ethylcellulose, butyl cellulose, and polyvinylalle 1.5 to 1 (3 parts by weight, tungsten paste or molybdenum paste prepared by mixing 1.5 to 10 parts by weight of at least one solvent selected from one terbione and glycol is most suitable.
- the formation position of the heating element 2 is eccentric in the thickness direction.
- the number of green sheets having the same thickness is laminated, and the ratio of the upper and lower configurations is set to 1Z1 to 1Z99. Specifically, 20 to 50 sheets are stacked on the upper side, and 5 to 20 sheets are stacked on the lower side.
- the granular powder was placed in a mold and formed into a flat plate to obtain a formed product.
- the green compact was drilled to provide a through hole 8 for inserting a semiconductor wafer-support pin, and a recess (not shown) for embedding a thermocouple.
- a conductive paste was printed on the ceramic substrate 1 obtained in (3) by screen printing.
- the printing pattern was a concentric pattern as shown in Fig. 1.
- Solvent PS603D manufactured by Toku Kagaku Kenkyusho, which is used to form through holes in printed wiring boards, was used.
- This conductive paste is a silver-Z-lead paste, which is composed of a metal oxide consisting of a mixture of lead oxide, zinc oxide, silica, boron oxide and alumina (the weight ratio of each is 5Z55 / 10/25/10), and silver paste. It contains 7.5 wt% of the amount.
- the silver used had a mean particle size of 4.5 ⁇ m and a flake shape.
- the ceramic substrate on which the conductive paste was printed was heated and fired at 780 ° C. to sinter silver and lead in the conductive paste, and baked on the ceramic substrate 1.
- the pattern made of the silver-lead lead sintered body 4 had a thickness of 5 m, a width of 2.4 lines, and a sheet resistivity of 7.7 ⁇ .
- the ceramic substrate 1 of (5) is immersed in an electroless nickel plating bath composed of a liquid, and a 1 im nickel metal layer 5 having a thickness of 1 im is deposited on the surface of the silver-lead lead sintered body 4 to generate heat.
- Body 2 formed.
- a solder layer (made by Tanaka Kikinzoku) 6 was formed by printing silver-lead solder paste from screen printing 1 on the part where terminals for securing the connection to the power supply were to be attached. Then, terminal pins 3 made of Kovar were placed on the solder layer 6 and heated and reflowed at 420 ° C. to attach the terminal pins 3 to the surface of the heating element 2.
- thermocouple (not shown) for temperature control was embedded to obtain a heater 1-10 (Figs. 1 and 2).
- Example 2 A heater made of silicon carbide ceramic substrate
- Example 2 Basically the same process as in Example 1, but using silicon carbide powder with an average particle size of 1.0 rn, sintering temperature of 190 ITC, and sintering the surface at 1500 ° C for 2 hours to obtain a thickness of 1 the ⁇ Rn to form S 1 ⁇ two layers.
- the followability of the temperature of the heating surface of the ceramic substrate to changes in voltage and current and the pull strength of the heating element 2 were measured. That is, when a voltage was applied to each heater, the heater of Example 1 showed a temperature change in .5 seconds, and the heater of Example 2 showed a temperature change in 2 seconds. On the other hand, with regard to the pull strength of the heat generating body 2, the heater of Example 1 was 3.1 kg / paint 2 , and the heater of Example 2 was 3 kg / country 2 .
- a semiconductor wafer with a diameter of 1.8 mm and 3.0 mm. 5.0 is provided with through-holes for inserting support pins and through-holes 38 for connecting the heat generator and terminal pins.
- a conductive paste was prepared by mixing 100 parts by weight of tungsten particles having an average particle diameter of 3 / ⁇ , 1.9 parts by weight of an acrylic binder, 3.7 parts by weight of a terbione solvent, and 0.2 parts by weight of a dispersant.
- the conductive paste was printed on the green sheet 31 by drawing a pattern by screen printing.
- the printing pattern was a concentric circle as shown in Fig. 1.
- the through-hole 3 8 for through-hole for connection to a terminal pin 3 7 sheets of conductive paste B Takashi ⁇ the c further, the green sheet 3 1 not printed with the conductive paste A on the upper side (heating surface)
- 17 sheets were laminated on the lower side, and were combined at 130 ° C. and a pressure of 80 kg / cm 2 to form a laminate (FIG. 3).
- the laminate was degreased in nitrogen gas at 600 ° C. for 5 hours, and hot-pressed at 1890 t and a pressure of 150 kg / cm 2 for 3 hours to obtain an aluminum nitride plate having a thickness of 3 countries. This was cut into a circular shape with a diameter of 230 o'clock, and a ceramic substrate 51 having a heating element of 6 mm in thickness and 1 mm in width was cut inside (Fig. 5 (a)).
- connection of the terminal pins 60 is desirably made to have a structure in which the terminal pins 60 are supported at three points by using the concave portions 48 in order to secure connection reliability.
- a plurality of thermocouples 61 for temperature control were buried in the hole 62 to obtain a ceramic heater (Fig. 5 (d)).
- a nichrome wire sandwiched by silicone rubber was used as a heating element.
- a 15 mm thick aluminum plate and a contact plate were sandwiched by the heating element and fixed with a port to form a heater. When a voltage was applied to the heater, it took 24 seconds for the temperature to change.
- Example 2 Basically the same as in Example 1, except that 100 parts by weight of alumina powder (average particle diameter: 1.0 m), 12 parts by weight of acrylic binder and 12 parts by weight of alcohol and a ligated material made of alcohol are granulated by a spray drier method.
- alumina powder average particle diameter: 1.0 m
- acrylic binder 12 parts by weight
- alcohol a ligated material made of alcohol
- Jo which was placed in a mold, and molded body is molded into a flat plate, the raw formed body 1200 ° C, and hot Topuresu at a pressure 200 kg / cm 2, to obtain an alumina substrate of 3 mm thick .
- tungsten particles having an average particle diameter of 3 ⁇ m 100 parts by weight of tungsten particles having an average particle diameter of 3 ⁇ m, 1.9 parts by weight of an acrylic binder, 3.7 parts by weight of «-terbione solvent, 0.2 parts by weight of a dispersant was mixed to form a conductive paste, which was printed.
- the ceramic substrate on which the conductive base was printed was heated and baked with lOOtTC to sinter tungsten.
- Example 4 Basically the same as in Example 4, except that the heating element is not a flat one, but the cross section is a square with a thickness of 20 mx 2 m2 and a width of 2 ⁇ m (1).
- the heating element is not a flat one, but the cross section is a square with a thickness of 20 mx 2 m2 and a width of 2 ⁇ m (1).
- Example 4 Basically the same as in Example 4, except that the printing conditions are changed, and the heating element is not flat, but has a cross-section of 5 x mx 72 widths (12000 ratio). Was used.
- Example 4 Basically the same as in Example 4, except that a green paste printed with a conductive paste is used.
- two sheets are stacked on the lower side and 25 sheets on the upper side, and the heating element is arranged at the center of the ceramic substrate.
- a force solver having the following composition was adjusted instead of the force solver PS603D which is basically the same as in Example 1.
- metal oxide lead oxide, zinc oxide, silica, boron oxide, alumina, weight ratio of each
- the sheet resistivity was 4 ⁇ .
- Nitrided aluminum powder (average particle size 1.1 ⁇ ) 100 parts by weight, yttria (yttrium oxide, average particle size 0.4 urn) 4 parts by weight, acrylic binder 1
- the composition consisting of 2 parts by weight and alcohol is granulated by a spray drier method.
- the green sheet was hot-pressed at 1800 ° (with a pressure of 200 kg / cm 2) to obtain an aluminum nitride substrate with a thickness of 3 mm. It was set to 1.
- sandblasting was performed with alumina powder having a diameter of 1 ⁇ m, and a groove having a width of 2.4 mm and a depth of 6 ⁇ m was formed at the position where the heating element was formed.
- a conductive paste was printed by screen printing to form a metal particle layer serving as a heating element.
- the pattern of the metal particle layer was a concentric pattern as shown in Fig. 1.
- the conductive paste is a solvent paste PS603D manufactured by Tokuka Kagaku Kenkyusho that is used to form through holes in printed wiring boards. used.
- This conductive paste is a silver Z lead paste, and a metal oxide composed of lead oxide, zinc oxide, silica, boron oxide, and alumina (the weight ratio of each is
- 5/5 5 X 10/25/5) is 7.5% by weight based on the amount of silver.
- the silver used was a flake with an average particle size of 4.5 m.
- the ceramic substrate on which the metal particle layer was formed was heated and fired at 780 ° C to sinter silver and lead in the metal particle layer (conductive paste) and baked on the ceramic substrate 1 .
- the pattern of the sintered body 4 of silver lead had a thickness of 5 mm, a width of 2.4 strokes, and a sheet resistivity of 7.7 mm ⁇ .
- the solder layer (made by Tanaka Kikinzoku) was formed by printing a silver-lead solder paste from screen printing 1 on the area where the terminal pins for securing the connection to the power supply were to be attached.
- terminal pins made of Kovar were placed on the solder layer 6, and heated and reflowed at 420 ° C. to attach the terminal pins to the surface of the heating element (see FIG. 6).
- the heating element is embedded in the ceramic substrate but is exposed from the surface. Further, the heating element as shown in FIG. 6B may be partially buried inside the ceramic substrate and partially exposed.
- Example 2 Basically the same as Example 1, except that lead oxide and zinc oxide were added to Solvent PS 6-3D to adjust the amount of metal oxide to 10%.
- the area resistance rate of the obtained heating element was 5 ⁇ / ⁇ ].
- Example 1 to 8 (excluding Example 3) and Comparative Examples 1 to 3, the time (response time) until a temperature change after voltage application was confirmed was measured. Also, the surface temperature The difference between the maximum temperature and the minimum temperature of the heated surface when the temperature was set to 60 (TC) was measured. In Examples 1 and 8, the pull strength (unit: kgZ 2 was measured.
- the ceramic heater of the present invention is practical because it is thin and light, and is used particularly for heating and drying the product in the field of the semiconductor industry.
- the ceramic heater according to the present invention uses nitride ceramic or carbide ceramic as the ceramic substrate and is thin, so that the heating surface can follow the temperature and the amount of change in the amount of current. Excellent and easy to control temperature. Furthermore, since the uniformity of the temperature distribution on the heated surface is excellent, semiconductor products can be dried efficiently.
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Description
Claims
Priority Applications (21)
Application Number | Priority Date | Filing Date | Title |
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KR1020007001061A KR20010022476A (ko) | 1999-06-09 | 1999-06-09 | 세라믹히터 및 그 제조방법 및 발열체용 도전 페이스트 |
EP99923983A EP1109423A1 (en) | 1999-06-09 | 1999-06-09 | Ceramic heater and method for producing the same, and conductive paste for heating element |
CN99800862A CN1296724A (zh) | 1999-06-09 | 1999-06-09 | 陶瓷加热器、其制造方法及用于加热体的导电膏 |
KR1020037000070A KR100544865B1 (ko) | 1999-06-09 | 1999-06-09 | 세라믹히터 및 발열체용 도전 페이스트 |
KR1020027008606A KR20020073158A (ko) | 1999-06-09 | 1999-06-09 | 세라믹히터 및 그 제조방법 |
PCT/JP1999/003086 WO2000076273A1 (fr) | 1999-06-09 | 1999-06-09 | Corps de chauffe en ceramique et procede de fabrication, et pate conductrice pour element chauffant |
JP2000151997A JP2001006852A (ja) | 1999-06-09 | 2000-05-23 | セラミックヒーター |
JP2000213518A JP3584203B2 (ja) | 1999-06-09 | 2000-06-09 | 半導体製造・検査装置用セラミック基板 |
JP2000174566A JP2001110878A (ja) | 1999-06-09 | 2000-06-09 | 半導体製造・検査装置用セラミック基板 |
JP2000174567A JP2001077182A (ja) | 1999-06-09 | 2000-06-09 | 半導体製造・検査装置用セラミック基板 |
JP2000174569A JP2001110879A (ja) | 1999-06-09 | 2000-06-09 | 半導体製造・検査装置用セラミック基板 |
JP2000174568A JP2001077183A (ja) | 1999-06-09 | 2000-06-09 | 半導体製造・検査装置用セラミック基板およびその製造方法 |
JP2000174574A JP3495689B2 (ja) | 1999-06-09 | 2000-06-09 | セラミックヒータ |
JP2002183564A JP2003109730A (ja) | 1999-06-09 | 2002-06-24 | セラミックヒーター |
JP2002183565A JP2003109731A (ja) | 1999-06-09 | 2002-06-24 | セラミックヒーター |
JP2002205644A JP2003163146A (ja) | 1999-06-09 | 2002-07-15 | 半導体製造・検査装置用セラミック基板 |
JP2002205491A JP2003158052A (ja) | 1999-06-09 | 2002-07-15 | 半導体製造・検査装置用セラミック基板 |
JP2002205422A JP2003151869A (ja) | 1999-06-09 | 2002-07-15 | 半導体製造・検査装置用セラミック基板 |
JP2002205460A JP2003158051A (ja) | 1999-06-09 | 2002-07-15 | 半導体製造・検査装置用セラミック基板 |
JP2002205526A JP2003158053A (ja) | 1999-06-09 | 2002-07-15 | 半導体製造・検査装置用セラミック基板およびその製造方法 |
JP2004171326A JP2004356638A (ja) | 1999-06-09 | 2004-06-09 | 半導体製造・検査装置用セラミック基板 |
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PCT/JP1999/003086 WO2000076273A1 (fr) | 1999-06-09 | 1999-06-09 | Corps de chauffe en ceramique et procede de fabrication, et pate conductrice pour element chauffant |
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EP (1) | EP1109423A1 (ja) |
JP (2) | JP2003109730A (ja) |
KR (3) | KR20020073158A (ja) |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003007661A1 (fr) * | 2001-07-09 | 2003-01-23 | Ibiden Co., Ltd. | Appareil de chauffage en ceramique et article en ceramique soude |
US6887316B2 (en) | 2000-04-14 | 2005-05-03 | Ibiden Co., Ltd. | Ceramic heater |
US7372001B2 (en) | 2002-12-17 | 2008-05-13 | Nhk Spring Co., Ltd. | Ceramics heater |
Families Citing this family (26)
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JP2001118662A (ja) | 1999-08-09 | 2001-04-27 | Ibiden Co Ltd | セラミックヒータ |
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JP2001196152A (ja) * | 2000-01-13 | 2001-07-19 | Sumitomo Electric Ind Ltd | セラミックスヒータ |
EP1189274A1 (en) | 2000-02-08 | 2002-03-20 | Ibiden Co., Ltd. | Ceramic board for semiconductor production and inspection devices |
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TWI281833B (en) | 2004-10-28 | 2007-05-21 | Kyocera Corp | Heater, wafer heating apparatus and method for manufacturing heater |
WO2006065062A1 (en) * | 2004-12-14 | 2006-06-22 | Hyung Woo Kim | A heating apparatus of wafer deposition substrate |
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US7777160B2 (en) * | 2007-12-17 | 2010-08-17 | Momentive Performance Materials Inc. | Electrode tuning method and apparatus for a layered heater structure |
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WO2017217251A1 (ja) * | 2016-06-17 | 2017-12-21 | トーカロ株式会社 | 発熱部材 |
CN110139406A (zh) * | 2019-06-10 | 2019-08-16 | 上海中孚特种油品有限公司 | 一种用于制备电热膜的饱和溶液及其制备方法 |
KR102239330B1 (ko) * | 2019-06-12 | 2021-04-12 | 엘지전자 주식회사 | 제어된 산화막을 가지는 면상 발열체 및 그 제조방법 |
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JPS57870A (en) * | 1980-06-04 | 1982-01-05 | Matsushita Electric Ind Co Ltd | Ceramic heater |
JPS5861591A (ja) * | 1981-10-08 | 1983-04-12 | 株式会社デンソー | セラミツクヒ−タ |
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JPH08273814A (ja) * | 1995-03-29 | 1996-10-18 | Ngk Spark Plug Co Ltd | セラミックヒーター |
JPH08273815A (ja) * | 1995-03-31 | 1996-10-18 | Ngk Spark Plug Co Ltd | 自己制御型セラミックヒーター |
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1999
- 1999-06-09 CN CN99800862A patent/CN1296724A/zh active Pending
- 1999-06-09 KR KR1020027008606A patent/KR20020073158A/ko active IP Right Grant
- 1999-06-09 EP EP99923983A patent/EP1109423A1/en not_active Withdrawn
- 1999-06-09 KR KR1020037000070A patent/KR100544865B1/ko not_active IP Right Cessation
- 1999-06-09 WO PCT/JP1999/003086 patent/WO2000076273A1/ja not_active Application Discontinuation
- 1999-06-09 KR KR1020007001061A patent/KR20010022476A/ko active Search and Examination
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2002
- 2002-06-24 JP JP2002183564A patent/JP2003109730A/ja active Pending
- 2002-06-24 JP JP2002183565A patent/JP2003109731A/ja active Pending
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JPS57870A (en) * | 1980-06-04 | 1982-01-05 | Matsushita Electric Ind Co Ltd | Ceramic heater |
JPS5861591A (ja) * | 1981-10-08 | 1983-04-12 | 株式会社デンソー | セラミツクヒ−タ |
JPH0651658A (ja) * | 1992-07-31 | 1994-02-25 | Toshiba Lighting & Technol Corp | 定着用ヒータ、定着用ヒータの製造方法および定着方法ならびに定着装置 |
JPH08273814A (ja) * | 1995-03-29 | 1996-10-18 | Ngk Spark Plug Co Ltd | セラミックヒーター |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6887316B2 (en) | 2000-04-14 | 2005-05-03 | Ibiden Co., Ltd. | Ceramic heater |
WO2003007661A1 (fr) * | 2001-07-09 | 2003-01-23 | Ibiden Co., Ltd. | Appareil de chauffage en ceramique et article en ceramique soude |
US7372001B2 (en) | 2002-12-17 | 2008-05-13 | Nhk Spring Co., Ltd. | Ceramics heater |
Also Published As
Publication number | Publication date |
---|---|
KR100544865B1 (ko) | 2006-01-24 |
JP2003109731A (ja) | 2003-04-11 |
KR20030022263A (ko) | 2003-03-15 |
CN1296724A (zh) | 2001-05-23 |
KR20020073158A (ko) | 2002-09-19 |
KR20010022476A (ko) | 2001-03-15 |
JP2003109730A (ja) | 2003-04-11 |
EP1109423A1 (en) | 2001-06-20 |
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