JP3171664B2 - Substrate suction device - Google Patents
Substrate suction deviceInfo
- Publication number
- JP3171664B2 JP3171664B2 JP15877492A JP15877492A JP3171664B2 JP 3171664 B2 JP3171664 B2 JP 3171664B2 JP 15877492 A JP15877492 A JP 15877492A JP 15877492 A JP15877492 A JP 15877492A JP 3171664 B2 JP3171664 B2 JP 3171664B2
- Authority
- JP
- Japan
- Prior art keywords
- titanium oxide
- pores
- less
- substrate
- suction
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000758 substrate Substances 0.000 title claims description 34
- 239000011148 porous material Substances 0.000 claims description 56
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 49
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 47
- 239000002245 particle Substances 0.000 claims description 24
- 239000012298 atmosphere Substances 0.000 claims description 23
- 239000000843 powder Substances 0.000 claims description 23
- 238000010304 firing Methods 0.000 claims description 20
- 238000001179 sorption measurement Methods 0.000 claims description 18
- 238000000465 moulding Methods 0.000 claims description 3
- 230000000052 comparative effect Effects 0.000 description 20
- 238000000034 method Methods 0.000 description 19
- 239000000919 ceramic Substances 0.000 description 13
- 239000002994 raw material Substances 0.000 description 12
- 239000004065 semiconductor Substances 0.000 description 10
- 238000005245 sintering Methods 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 239000000428 dust Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 230000005611 electricity Effects 0.000 description 4
- 239000012299 nitrogen atmosphere Substances 0.000 description 4
- 230000003068 static effect Effects 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 3
- 238000007606 doctor blade method Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000012300 argon atmosphere Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000012212 insulator Substances 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 101100321304 Bacillus subtilis (strain 168) yxdM gene Proteins 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000007786 electrostatic charging Methods 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
Landscapes
- Manipulator (AREA)
- Container, Conveyance, Adherence, Positioning, Of Wafer (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、薄板を吸着移動又は吸
着固定する吸着板を備えた基板吸着装置に関し、特に半
導体ウエハ等の薄板を吸着して移動したり、吸着固定す
るウエハハンド又はウエハホルダに係る基板吸着装置に
関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a substrate suction apparatus provided with a suction plate for sucking and moving or fixing a thin plate, and more particularly to a wafer hand or wafer holder for sucking and moving a thin plate such as a semiconductor wafer or for holding it by suction. The present invention relates to a substrate suction device according to the above.
【0002】[0002]
【従来の技術】半導体集積回路の製造装置に組み込まれ
るウエハハンド及びウエハホルダは、吸着板を通じて、
真空吸着によりウエハを移動するため及びウエハを真空
吸着固定するために使用されている。このウエハハンド
及びウエハホルダ用吸着板としては、従来、アルミナで
作製された吸着板、即ち、絶縁体であるアルミナ製の吸
着板が使用されている。2. Description of the Related Art A wafer hand and a wafer holder incorporated in a semiconductor integrated circuit manufacturing apparatus are passed through a suction plate.
It is used to move a wafer by vacuum suction and to fix the wafer by vacuum suction. As the suction plate for the wafer hand and the wafer holder, a suction plate made of alumina, that is, a suction plate made of alumina, which is an insulator, is conventionally used.
【0003】[0003]
【発明が解決しようとする課題】ところで、ICの製造
工程では、極端にゴミが嫌われており、このゴミに対す
る配慮がなされているが、従来のアルミナ製吸着板の場
合、この吸着板に静電気が帯電しやすく、この静電気に
よりゴミが吸着しやすい欠点を有している。この欠点を
解消するために、即ち、アルミナ製吸着板に帯電する静
電気を除去するために、この吸着板に導体をコ−ティン
グする等の手段が従来から提案されている。By the way, in the process of manufacturing an IC, dust is extremely hated, and such dust is taken into consideration. However, in the case of a conventional alumina suction plate, the electrostatic suction is applied to the suction plate. Have a disadvantage that they are easily charged and dust is easily absorbed by the static electricity. In order to solve this drawback, that is, to remove static electricity charged on the alumina suction plate, means for coating a conductor on the suction plate have been conventionally proposed.
【0004】しかしながら、導体をコ−ティングする手
段では、煩雑な工程を必要とする等問題点が多く、その
ため、このような手段を要しないセラミック製吸着板が
望まれていた。即ち、従来の絶縁体であるアルミナ製の
吸着板と異なり、比抵抗が小さく、静電気が帯電しない
セラミック製吸着板が要望されている。[0004] However, the means for coating the conductor has many problems, such as the necessity of complicated steps. Therefore, a ceramic suction plate which does not require such means has been desired. That is, unlike a conventional suction plate made of alumina, which is an insulator, a ceramic suction plate which has a small specific resistance and is not charged with static electricity is demanded.
【0005】また、吸着板表面に多数のポア−が存在す
る場合、特に大径のポア−(例えば3μm径以上のポア
−)が多数存在すると、(a) このポアーにゴミ、塵埃な
どが付着し、これが半導体製造工程中に混入する等の問
題が生じ、さらには、(b) このポアー内にガスなどが吸
着し、そのため半導体ウエハ等の薄板の吸着能、保持能
を低下させる、という問題が生ずる。When a large number of pores are present on the surface of the suction plate, especially when a large number of pores (for example, pores having a diameter of 3 μm or more) are present, (a) dust and dirt adhere to the pores. However, this causes problems such as being mixed during the semiconductor manufacturing process.Furthermore, (b) a problem that gas or the like is adsorbed in the pores, thereby lowering the adsorbing ability and holding ability of a thin plate such as a semiconductor wafer. Occurs.
【0006】従って、前記要望に加え、さらに上記問題
点(a)及び(b)をも解消する吸着板、即ち、比抵抗が小さ
く、しかも、吸着板表面にポア−が極めて少ないセラミ
ック製吸着板の出現が今日強く要望されている。Therefore, in addition to the above-mentioned demands, an adsorption plate which also solves the above problems (a) and (b), that is, a ceramic adsorption plate having a small specific resistance and having very few pores on the surface of the adsorption plate. The emergence of is strongly desired today.
【0007】そこで、本発明は、上記要望に沿うセラミ
ック製吸着板を備えた基板吸着装置を提供することを目
的とする。詳細には、本発明の目的は、比抵抗が小さ
く、しかも、表面にポア−が極めて少ないセラミック製
吸着板を備えた基板吸着装置を提供するにあり、静電気
対策が容易であり、半導体の高集積化、高歩留まりに大
きく貢献することができるセラミック製吸着板を備えた
基板吸着装置を提供するにある。Accordingly, an object of the present invention is to provide a substrate suction device provided with a ceramic suction plate meeting the above demand. More specifically, an object of the present invention is to provide a substrate suction device provided with a ceramic suction plate having a low specific resistance and having very few pores on its surface. An object of the present invention is to provide a substrate suction device provided with a ceramic suction plate which can greatly contribute to integration and a high yield.
【0008】[0008]
【課題を解決するための手段】そして、本発明は、セラ
ミック製吸着板として酸化チタン製の吸着板を使用する
ものであって、この吸着板の比抵抗が1.0Ω・cm以下
であり、かつ、その表面に存在する3μm径以上のポア
−数が100個/mm2以下である吸着板を用いることを特
徴とし、これによって上記目的とする基板吸着装置を提
供するものである。According to the present invention, a titanium oxide adsorbing plate is used as a ceramic adsorbing plate, and the specific resistance of the adsorbing plate is 1.0 Ω · cm or less, and The present invention is characterized in that an adsorbing plate having a number of pores having a diameter of 3 μm or more and having a diameter of not more than 100 / mm 2 existing on the surface thereof is used, thereby providing the above-mentioned substrate adsorbing apparatus.
【0009】即ち、本発明は、「薄板を吸着移動又は吸
着固定する吸着板を備えた基板吸着装置であって、上記
吸着板の比抵抗が1.0Ω・cm以下であり、かつ、その
表面に存在する3μm径以上のポア−数が1mm2当た
り100個以下である酸化チタン製吸着板を備えてなるこ
とを特徴とする基板吸着装置。」を要旨とするものであ
る。That is, the present invention provides a substrate suction apparatus provided with a suction plate for sucking and moving or fixing a thin plate, wherein the specific resistance of the suction plate is 1.0 Ω · cm or less, and A substrate adsorption device comprising a titanium oxide adsorption plate having a number of pores having a diameter of 3 μm or more and not more than 100 per 1 mm 2. "
【0010】以下、本発明を詳細に説明すると、本発明
者等は、比抵抗の小さなセラミックであって、しかも、
表面にポア−が極めて少ない平滑なセラミックの製造法
について鋭意研究した結果、次の(1)〜(3)の製造法によ
れば、目的とするセラミック製吸着板が得られることを
見出し、本発明を完成したものである。 (1) 高純度酸化チタン微粉末を成形した後、この成形体
を大気又は不活性雰囲気中で焼成し、さらにHIP処理
する方法。 (2) 高純度酸化チタン微粉末を成形した後、還元雰囲気
中で焼成する方法。 (3) 高純度酸化チタン微粉末を成形した後、還元雰囲気
中で焼成し、さらにHIP処理する方法。Hereinafter, the present invention will be described in detail. The present inventors have made ceramics having a small specific resistance, and
As a result of diligent research on a method for producing a smooth ceramic having extremely few pores on the surface, it was found that the target ceramic adsorbing plate can be obtained by the following methods (1) to (3). The invention has been completed. (1) A method in which a high-purity titanium oxide fine powder is molded, and then the molded body is fired in air or an inert atmosphere, and further subjected to HIP treatment. (2) A method in which high-purity titanium oxide fine powder is molded and then fired in a reducing atmosphere. (3) A method in which high-purity titanium oxide fine powder is molded, fired in a reducing atmosphere, and further subjected to HIP treatment.
【0011】即ち、本発明は、“比抵抗が極めて小さ
い”という本発明で意図する第1の性質及び“表面にポ
ア−が極めて少ない”という同じく本発明で意図する第
2の性質をあわせ持つセラミック製吸着板を提供するこ
とを技術的課題とする。そして、上記(1)〜(3)の製造法
によれば、上記第1及び第2の両性質をあわせ持つ酸化
チタン焼結体、即ち、「比抵抗が1.0Ω・cm以下であ
り、かつ、その表面に存在する3μm径以上のポア−数
が100個/mm2以下の酸化チタン焼結体。」が得られる
ことを見いだし、この酸化チタン焼結体を基板吸着装置
用の吸着板として使用する本発明を完成したものであ
る。That is, the present invention has both the first property intended by the present invention that "the resistivity is extremely small" and the second property intended by the present invention that "there are very few pores on the surface". A technical object is to provide a ceramic suction plate. According to the production methods (1) to (3), the titanium oxide sintered body having both the first and second properties, that is, “the specific resistance is 1.0 Ω · cm or less, and And a titanium oxide sintered body having a number of pores having a diameter of not less than 3 μm and having a diameter of not more than 100 / mm 2 existing on the surface thereof. ”This titanium oxide sintered body is used as an adsorption plate for a substrate adsorption device. The present invention to be used has been completed.
【0012】上記(1)〜(3)の製造法において、原料とし
て使用する「高純度酸化チタン微粉末」としては、99%
以上の高純度のものを用いるのが好ましい。99%未満で
は、本発明で意図する第2の性質である“表面にポア−
が極めて少ない焼結体(3μm径以上のポア−数が100個
/mm2以下の焼結体)”が得られ難いので、好ましく
ない(後記比較例6、7参照)。In the above production methods (1) to (3), the “high-purity titanium oxide fine powder” used as a raw material is 99%
It is preferable to use one having the above high purity. If it is less than 99%, the second property intended in the present invention, which is "a pore on the surface,
(A sintered body having a pore number of 3 μm or more and a pore number of 100 / mm 2 or less) ”is not preferable (see Comparative Examples 6 and 7 described later).
【0013】また、上記原料微粉末の平均粒子径として
は、1μm以下のものを用いるのが好ましい 。1μm
をこえる粗い粉末を使用すると、同じく本発明で意図す
る第2の性質である“表面にポア−が極めて少ない焼結
体”が得られ難いので、好ましくない(後記比較例8参
照)。Further, it is preferable to use the raw material fine powder having an average particle diameter of 1 μm or less. 1 μm
If a coarse powder is used, the second property, "sintered body having extremely few pores on the surface", which is also intended in the present invention, is difficult to obtain, which is not preferable (see Comparative Example 8 described later).
【0014】原料として使用する「高純度酸化チタン微
粉末」について更に説明すると、この原料粉末として、
純度が99%未満の場合、また、平均粒子径が1μmより
粗い場合、後記するように、低温易焼結の性質が失われ
てしまい、充分に焼結密度が上がらない。そして、焼結
密度を上げるため、高温(本発明で規定する1300℃を越
える温度、例えば1400℃、1600℃)で焼結すると、粒成
長が生じ、ポア−が粗大化してしまう(後記比較例2〜8
参照)。The “high-purity titanium oxide fine powder” used as a raw material will be further described.
If the purity is less than 99%, or if the average particle size is coarser than 1 μm, the properties of low-temperature easy sintering will be lost and the sintered density will not be sufficiently increased as described later. When sintering at a high temperature (a temperature exceeding 1300 ° C. defined in the present invention, for example, 1400 ° C., 1600 ° C.) to increase the sintering density, grain growth occurs and pores become coarse (comparative examples described later). 2-8
reference).
【0015】従って、本発明において、原料として使用
する「高純度酸化チタン微粉末」としては、99%以上の
高純度で1μm以下の平均粒子径のものを用いるのが好
ましく、「99.8%以上の高純度で0.5μm以下の平均粒
子径の酸化チタン微粉末」を使用するのがより好まし
い。Therefore, in the present invention, as the “high-purity titanium oxide fine powder” to be used as a raw material, it is preferable to use a powder having a high purity of 99% or more and an average particle diameter of 1 μm or less. It is more preferable to use "high-purity titanium oxide fine powder having an average particle diameter of 0.5 μm or less".
【0016】本発明において、上記原料微粉末を通常の
CIP成形法によるか或いはドクタ−ブレイド法又は押
出法等により成形し、セラミックグリ−ンシ−ト化す
る。ドクタ−ブレイド法又は押出法により成形したもの
については、その後必要に応じ脱バインダ−処理する。
次に、下記(1)〜(3)のいずれかの方法を採用して焼成
し、本発明で意図する前記第1及び第2の両性質をあわ
せ持つ酸化チタン製基板を製造する。 (1) 大気又は不活性雰囲気中で焼成し、さらにHIP処
理する方法。 (2) 還元雰囲気中で焼成する方法。 (3) 還元雰囲気中で焼成し、さらにHIP処理する方
法。In the present invention, the above raw material fine powder is formed by a usual CIP molding method or by a doctor blade method or an extrusion method, etc., and formed into a ceramic green sheet. Those molded by the doctor blade method or the extrusion method are then subjected to binder removal treatment as required.
Next, firing is performed by using any of the following methods (1) to (3) to produce a titanium oxide substrate having both the first and second properties intended in the present invention. (1) A method of firing in air or an inert atmosphere and further performing HIP treatment. (2) A method of firing in a reducing atmosphere. (3) A method of firing in a reducing atmosphere and further performing HIP treatment.
【0017】上記(1)〜(3)の方法において、大気又は還
元雰囲気中での焼成温度としては、1100〜1300℃が好ま
しく、1200℃前後がより好ましい。1100℃未満の低温焼
成では、焼結自体進行しにくいので酸化チタン焼結体が
得られ難く、一方、1300℃をこえる焼成温度では、本発
明で意図する第2の性質である“表面にポア−が極めて
少ない焼結体(3μm径以上のポア−数が100個/mm2
以下の焼結体)”が得られ難いので、好ましくない(後
記比較例2参照)。In the above methods (1) to (3), the firing temperature in the air or in a reducing atmosphere is preferably from 1100 to 1300 ° C., and more preferably around 1200 ° C. At a low temperature firing of less than 1100 ° C, it is difficult to obtain a titanium oxide sintered body because sintering itself does not proceed easily. On the other hand, at a firing temperature exceeding 1300 ° C, the second property, “porous surface -Sintered body with very few (100 / mm 2 pores with a diameter of 3 μm or more)
The following sintered bodies) ”are not preferred because they are difficult to obtain (see Comparative Example 2 below).
【0018】上記焼成温度について更に説明すると、本
発明では、チタニアセラミックで通常採用されている焼
成温度(1350℃程度)よりも低温である「1100〜1300
℃」で大気、不活性雰囲気又は還元雰囲気中で焼成する
ものであり、1300℃を越える温度では、粒成長(結晶成
長)が著しく、ポア−の粒界相への移動と粒成長に伴う
ポア−の粗大化が生じるので、好ましくない。そして、
本発明では、このような低温での焼結を容易に行わせる
ため(低温易焼結性を発揮させるため)、前記した99%
以上の高純度で1μm以下の平均粒子径の「高純度酸化
チタン微粉末」を原料として使用するものである。The firing temperature will be further described. In the present invention, "1100 to 1300" which is lower than the firing temperature (about 1350 ° C.) usually used for titania ceramics.
° C ”in air, inert atmosphere or reducing atmosphere. At temperatures exceeding 1300 ° C, grain growth (crystal growth) is remarkable, and pores move to the grain boundary phase and pores accompanying grain growth. This is not preferable because coarsening of-occurs. And
In the present invention, in order to easily perform sintering at such a low temperature (to exhibit low-temperature sinterability), the aforementioned 99%
The above-mentioned “high-purity titanium oxide fine powder” having a high purity and an average particle diameter of 1 μm or less is used as a raw material.
【0019】前記(1)の方法において、大気又は不活性
雰囲気中の焼成のみでは、本発明で意図する第1の性質
である“比抵抗が小さい焼結体(1.0Ω・cm以下の比
抵抗を有する焼結体)”が得られない(後記比較例1参
照)。そこで、この大気又は不活性雰囲気中の焼成法を
採用する場合、上記第1の性質“比抵抗が小さいという
性質”を付与するため、得られた焼結体に対しさらにH
IP処理することが必要である。In the above method (1), the sintering with a small specific resistance (specific resistance of 1.0 Ω · cm or less), which is the first property intended by the present invention, is achieved only by firing in the air or an inert atmosphere. Is not obtained (see Comparative Example 1 described later). Therefore, when the sintering method in the air or in an inert atmosphere is adopted, the obtained sintered body is further subjected to H in order to impart the first property described above, that is, the property of having a small specific resistance.
It is necessary to perform IP processing.
【0020】このHIP処理、例えばカ−ボンヒ−タの
使用によるHIP処理により、大気又は不活性雰囲気中
で焼成した酸化チタン焼結体が半導体化し、所望の1.0
Ω・cm以下の比抵抗を有するものが得られる。なお、
このHIP処理により比抵抗を小さくする作用以外に表
面のポア−をより少なくすることができる作用も生ず
る。このHIP処理としては、粒成長によるポア−の粗
大化を生じさせないという点から、前記焼成温度(1100
〜1300℃)以下の800〜1100℃で行うのが好ましく、ま
た、圧力としては、500kg/cm2以上で行うのが好ま
しい。より好ましいHIP処理条件は、1000℃、1500k
g/cm2である。By this HIP treatment, for example, HIP treatment using carbon heater, the titanium oxide sintered body fired in the air or an inert atmosphere is converted into a semiconductor, and a desired 1.0% is obtained.
Those having a specific resistance of Ω · cm or less can be obtained. In addition,
In addition to the effect of reducing the specific resistance, the HIP treatment also has the effect of reducing the number of pores on the surface. The HIP treatment is performed at the firing temperature (1100) because the pores do not become coarse due to grain growth.
(1300 ° C.) or lower at 800 to 1100 ° C., and the pressure is preferably 500 kg / cm 2 or more. More preferred HIP processing conditions are 1000 ° C. and 1500 k
g / cm 2 .
【0021】前記(2)の「還元雰囲気中で焼成する」方
法では、還元雰囲気中で焼成することにより、酸化チタ
ンが部分的に還元され、半導体化し、所望の1.0Ω・c
m以下の比抵抗を有するものが得られる。この還元雰囲
気としては、焼成時に酸化チタンが半導体化する雰囲気
であれば任意の還元性雰囲気で焼成することができる
が、例えばカ−ボンヒ−タ等の使用による窒素雰囲気中
で焼成するのが好ましい。In the method (2) of “calcining in a reducing atmosphere”, the titanium oxide is partially reduced by baking in a reducing atmosphere to be converted into a semiconductor, and a desired 1.0 Ω · c
Those having a specific resistance of not more than m are obtained. As this reducing atmosphere, firing can be performed in any reducing atmosphere as long as titanium oxide becomes a semiconductor during firing, but firing in a nitrogen atmosphere using, for example, a carbon heater is preferable. .
【0022】この(2)の還元雰囲気中で1100〜1300℃で
焼成する方法により、“比抵抗が極めて小さい”という
本発明で意図する第1の性質及び“表面にポア−が極め
て少ない”という同じく本発明で意図する第2の性質を
あわせ持つ酸化チタン焼結体が得られる。また、本発明
において、表面のポア−をより少なくするため、上記
(2)の方法で得られた酸化チタン焼結体をさらに前記し
た例えばカ−ボンヒ−タの使用によるHIP処理をする
ことができる。このHIP処理としては、前記(1)のH
IP処理と同様、焼成温度800〜1100℃で圧力500kg/
cm2以上で行うのが好ましく、1000℃、1500kg/c
m2で行うのがより好ましい。According to the method (2) of baking at 1100 to 1300 ° C. in a reducing atmosphere, the first property of the present invention that “specific resistance is extremely small” and “the surface has very few pores” Similarly, a titanium oxide sintered body having the second property intended in the present invention is obtained. Further, in the present invention, in order to further reduce the surface pores,
The titanium oxide sintered body obtained by the method (2) can be further subjected to HIP treatment using, for example, a carbon heater as described above. This HIP processing includes the H (1) described above.
As with IP treatment, at a firing temperature of 800 to 1100 ° C and a pressure of 500 kg /
cm 2 or more, preferably 1000 ° C., 1500 kg / c
More preferably, it is performed at m 2 .
【0023】本発明では、以上の(1)〜(3)の方法で得ら
れた酸化チタン製基板に必要に応じてその表面を平面研
削及びラップ処理を施すことができる。そして、この酸
化チタン製基板に吸引用孔を穿孔して酸化チタン製吸着
板を得るものである。In the present invention, the surface of the titanium oxide substrate obtained by the above methods (1) to (3) can be subjected to surface grinding and lapping as required. Then, a suction hole is formed in the titanium oxide substrate to obtain a titanium oxide adsorption plate.
【0024】[0024]
【実施例】以下、本発明の実施例を比較例と共に挙げ、
本発明をより詳細に説明する。 (実施例1)平均粒径0.25μm、純度99.8%の酸化チタ
ン粉末にポリビニルブチラ−ルとエチルアルコ−ルを加
えて混合し、スラリ−化した後、ドクタ−ブレイド法に
よりグリ−ンシ−トを作製し、脱バインダ−処理後大気
中で1200℃で焼成した。次に、この焼結体をアルゴン雰
囲気中で1000℃の温度、1500kg/cm2の圧力でカ−
ボンヒ−タを有するHIP炉でHIP処理した。EXAMPLES Examples of the present invention will be described below together with comparative examples.
The present invention will be described in more detail. (Example 1) Polyvinyl butyral and ethyl alcohol were added to a titanium oxide powder having an average particle diameter of 0.25 µm and a purity of 99.8%, mixed and slurried, and then greened by a doctor blade method. Was prepared and fired at 1200 ° C. in the air after the binder removal treatment. Next, the sintered body is subjected to carraging in an argon atmosphere at a temperature of 1000 ° C. and a pressure of 1500 kg / cm 2.
HIP treatment was performed in a HIP furnace having a bon heater.
【0025】得られた酸化チタン製基板について、比抵
抗及びポア−数を測定し、その結果を表1に示した。な
お、この基板の表面に30μm径以上のポア−が認められ
なかった。上記の比抵抗は、4端子法(1V,1kHz)にて
測定した。また、基板表面のポア−の径及び個数は、走
査型電子顕微鏡で観察し、得られた像の写真を使用して
測定した。なお、表1中の比抵抗値は、25℃で測定した
値であり、また、ポア−数は、平均粒径3μm以上の個
数/mm2である。The specific resistance and the number of pores of the obtained titanium oxide substrate were measured, and the results are shown in Table 1. No pores having a diameter of 30 μm or more were observed on the surface of the substrate. The above specific resistance was measured by a four-terminal method (1 V, 1 kHz). The diameter and number of pores on the substrate surface were observed with a scanning electron microscope, and measured using photographs of the obtained images. The specific resistance values in Table 1 are values measured at 25 ° C., and the number of pores is the number of particles having an average particle diameter of 3 μm or more / mm 2 .
【0026】(実施例2)平均粒径0.25μm、純度99.8
%の酸化チタン粉末にポリビニルブチラ−ルとエチルア
ルコ−ルを加えて混合し、スラリ−化した後、ドクタ−
ブレイド法によりグリ−ンシ−トを作製し、脱バインダ
−処理をした後窒素雰囲気中でカ−ボンヒ−タにより12
00℃で焼成した。得られた酸化チタン製基板について、
実施例1と同様、比抵抗及びポア−数を測定し、その結
果を表1に示した。なお、この基板表面には30μm径以
上のポア−が皆無であった。Example 2 Average particle size 0.25 μm, purity 99.8
% Titanium oxide powder, polyvinyl butyral and ethyl alcohol were added and mixed to form a slurry.
A green sheet is prepared by a blade method, debindered, and subjected to carbon heating in a nitrogen atmosphere.
It was fired at 00 ° C. About the obtained titanium oxide substrate,
As in Example 1, the specific resistance and the number of pores were measured, and the results are shown in Table 1. The surface of the substrate had no pores having a diameter of 30 μm or more.
【0027】(実施例3)実施例2で得られた焼結体を
前記実施例1と同様、アルゴン雰囲気中で1000℃の温
度、1500kg/cm2の圧力でカ−ボンヒ−タを有する
HIP炉でHIP処理した。得られた酸化チタン製基板
について、実施例1と同様、比抵抗及びポア−数を測定
し、その結果を表1に示した。なお、この基板表面には
30μm径以上のポア−が皆無であった。(Example 3) A HIP having a carbon heater at a temperature of 1000 ° C and a pressure of 1500 kg / cm 2 in an argon atmosphere was prepared in the same manner as in Example 1 except that the sintered body obtained in Example 2 was used. HIPed in the furnace. For the obtained titanium oxide substrate, the specific resistance and the number of pores were measured as in Example 1, and the results are shown in Table 1. The surface of this substrate
There were no pores having a diameter of 30 μm or more.
【0028】(実施例4)平均粒径0.7μm、純度99.2
%の酸化チタン粉末を使用する点を除いて前記実施例1
と同一手段で酸化チタン製基板を得た。得られた酸化チ
タン製基板について、実施例1と同様、比抵抗及びポア
−数を測定し、その結果を表1に示した。なお、この基
板表面には30μm径以上のポア−が皆無であった。Example 4 Average particle size 0.7 μm, purity 99.2
% Of the titanium oxide powder of Example 1 except that
A substrate made of titanium oxide was obtained in the same manner as described above. For the obtained titanium oxide substrate, the specific resistance and the number of pores were measured as in Example 1, and the results are shown in Table 1. The surface of the substrate had no pores having a diameter of 30 μm or more.
【0029】(比較例1〜8)なお、比較のため、表1
に示す平均粒径、純度の酸化チタン粉末を使用し、前記
実施例1と同様な方法でグリ−ンシ−トを作製し、脱バ
インダ−した後、同じく表1に示す常圧焼結条件で(比
較例3、5、7、8ではさらに表1に示すHIP処理条
件で)焼成して酸化チタン製基板を得た。得られた各酸
化チタン製基板について、前記実施例1と同様、比抵抗
及びポア−数を測定し、その結果を表1に示した。(Comparative Examples 1 to 8) For comparison, Table 1
Using a titanium oxide powder having an average particle size and purity shown in Table 1, a green sheet was prepared in the same manner as in Example 1 and then debindered. (Comparative Examples 3, 5, 7, and 8 were further fired under the HIP processing conditions shown in Table 1) to obtain a titanium oxide substrate. For each of the obtained titanium oxide substrates, the specific resistance and the number of pores were measured in the same manner as in Example 1, and the results are shown in Table 1.
【0030】(比較例9)更に、比較のため、平均粒径
0.6μm、純度99.8%の酸化アルミニウム粉末を使用
し、前記実施例1と同様な方法でグリ−ンシ−トを作製
し、脱バインダ−した後大気中で1600℃で焼成した。得
られた酸化アルミニウム焼結体について、前記実施例1
と同様、比抵抗及びポア−数を測定し、その結果を表1
に示した。Comparative Example 9 Further, for comparison, the average particle size was
A green sheet was prepared in the same manner as in Example 1 above, using aluminum oxide powder having a purity of 0.6 μm and a purity of 99.8%. After removing the binder, the green sheet was fired at 1600 ° C. in the air. About the obtained aluminum oxide sintered compact, the said Example 1
In the same manner as in Example 1, the specific resistance and the number of pores were measured.
It was shown to.
【0031】[0031]
【表1】 [Table 1]
【0032】表1から明らかなように、平均粒径0.25μ
m、純度99.8%の酸化チタン粉末を成形した後、大気中
で1200℃で焼成し、さらに還元雰囲気中で1000℃、1500
kg/cm2の圧力でHIP処理を行った実施例1で
は、比抵抗が0.7Ω・cmでポア−数が34個/mm2のも
のが得られた。また、実施例1と同一原料を用い、窒素
雰囲気中で1200℃で焼成した実施例2では、比抵抗が0.
9Ω・cmでポア−数が70個/mm2のものが得られた。As is clear from Table 1, the average particle size is 0.25 μm.
m, 99.8% pure titanium oxide powder, molded, fired at 1200 ° C in air, and further reduced to 1000 ° C, 1500 ° C
In Example 1 in which the HIP treatment was performed at a pressure of kg / cm 2 , a sample having a specific resistance of 0.7 Ω · cm and a pore number of 34 / mm 2 was obtained. Further, in Example 2, which was fired at 1200 ° C. in a nitrogen atmosphere using the same raw material as in Example 1, the specific resistance was 0.3.
A sample having a pore number of 70 / mm 2 at 9 Ω · cm was obtained.
【0033】この実施例2で得られたものを更にHIP
処理を行った実施例3では、比抵抗が0.7Ω・cmでポ
ア−数が38個/mm2のものが得られ、HIP処理によ
り比抵抗及びポア−数とも改善されることが理解できる
(比抵抗:0.9→0.7、ポア−数:70→38)。更に、平均
粒径0.7μm、純度99.2%の酸化チタン粉末(実施例1
より平均粒径が大であり、低純度の原料であるが、いず
れも本発明の範囲内の原料)を使用し、実施例1と同様
大気中で焼成し、更にHIP処理を行った実施例4で
は、比抵抗が実施例1と同じ0.7Ω・cmであり、ポア
−数については、実施例1より多いけれども本発明で意
図する100個/mm2以内の92個/mm2のものが得られ
た。The product obtained in Example 2 was further subjected to HIP
In Example 3 in which the treatment was performed, a specific resistance of 0.7 Ω · cm and a number of pores of 38 / mm 2 was obtained, and it can be understood that both the specific resistance and the number of pores were improved by the HIP treatment ( Specific resistance: 0.9 → 0.7, number of pores: 70 → 38). Further, titanium oxide powder having an average particle size of 0.7 μm and a purity of 99.2% (Example 1)
Examples in which raw materials having a larger average particle size and a low purity were used, but all of which were within the scope of the present invention), were fired in the air in the same manner as in Example 1, and were further subjected to HIP treatment. in 4, the same 0.7Ω · cm resistivity as in example 1, the pore - the number, those of the examples 1 100 contemplated more but the present invention / mm 2 within 92 amino / mm 2 Obtained.
【0034】一方、実施例1と同一条件であるが、HI
P処理を行わない比較例1では、ポア−数が70個/mm
2であるが、1012Ω・cmという高比抵抗のもの(実施
例1では0.7Ω・cm)が得られ、本発明で意図する
“比抵抗が小さい焼結体(1.0Ω・cm以下の比抵抗を
有する焼結体)”が得られなかった。また、実施例1に
おける大気中での焼成温度を1600℃とし、HIP処理を
行わない比較例2及びこの比較例2で得られたものをH
IP処理(1400℃、1500kg/cm2)した比較例3で
は、いずれも高比抵抗(1012Ω・cm)であるばかりで
なく、ポア−数が840個/mm2及び480個/mm2であっ
た。On the other hand, under the same conditions as in the first embodiment,
In Comparative Example 1 in which the P treatment was not performed, the number of pores was 70 / mm.
2 , a product having a high specific resistance of 10 12 Ω · cm (0.7 Ω · cm in Example 1) was obtained. (A sintered body having specific resistance) "was not obtained. Further, in Example 1, the firing temperature in the atmosphere was set to 1600 ° C., and the HIP treatment was not performed.
In Comparative Example 3 subjected to IP treatment (1400 ° C., 1500 kg / cm 2 ), not only the high specific resistance (10 12 Ω · cm) but also the number of pores was 840 / mm 2 and 480 / mm 2. Met.
【0035】更に、実施例2における窒素雰囲気中での
焼成温度を1600℃とし、HIP処理を行わない比較例4
及びこの比較例4で得られたものをHIP処理(1400
℃、1500kg/cm2)した比較例5では、いずれも0.8
Ω・cmという低比抵抗であるが、ポア−数は920個/
mm2及び770個/mm2であった。また、平均粒径は、
本発明の範囲内であり、実施例4と同一の0.7μmを用
いたが、純度が本発明の範囲外の92.0%の原料を使用
し、大気中で焼成(1400℃)した比較例6では、1012Ω
・cmの高比抵抗、960個/mm2のポア−数のものが得
られた。Further, Comparative Example 4 in which the firing temperature in the nitrogen atmosphere in Example 2 was 1600 ° C. and the HIP treatment was not performed
And the product obtained in Comparative Example 4 was subjected to HIP treatment (1400
℃, 1500 kg / cm 2 ) in Comparative Example 5
Although the resistivity is as low as Ω · cm, the number of pores is 920 /
It was mm 2 and 770 pieces / mm 2. The average particle size is
In Comparative Example 6, which was within the scope of the present invention and used the same 0.7 μm as in Example 4, but using a 92.0% raw material having a purity outside the scope of the present invention and calcined (1400 ° C.) in air. , 10 12 Ω
・ High specific resistance of cm and a pore number of 960 / mm 2 were obtained.
【0036】上記比較例6と同じ原料を使用し、大気中
で焼成し、さらにHIP処理(1200℃、1800kg/cm
2)を行った比較例7では、HIP処理を施したことに
より比抵抗は0.8Ω・cmであったが、低純度(92.0
%)の原料を使用し、本発明の範囲外の温度(1400℃)
で大気中で焼成したことにより、550個/mm2のポアー
数のものが得られた。The same raw material as in Comparative Example 6 was used, fired in the air, and further subjected to HIP treatment (1200 ° C., 1800 kg / cm
In Comparative Example 7 in which 2 ) was performed, the specific resistance was 0.8 Ω · cm due to the HIP treatment, but the low purity (92.0
%), And the temperature outside the range of the present invention (1400 ° C)
By baking in the air at, a pore number of 550 / mm 2 was obtained.
【0037】更に、原料の純度は本発明の範囲内である
99.2%であるが、平均粒径は本発明の範囲外の2.1μm
の原料を使用し、大気中で焼成(1400℃)し、さらにH
IP処理(1200℃、1800kg/cm2)を行った比較例
8では、比抵抗は0.8Ω・cmであったが、310個/mm
2のポア−数のものが得られた。なお、アルミナ焼結体
(原料純度99.8%、平均粒径0.6μm、大気中での焼
成)である比較例9では、1014Ω・cmという高比抵抗
であるばかりでなく、ポア−数が1000個/mm2であっ
た。Further, the purity of the raw material is within the scope of the present invention.
99.2%, but the average particle size is 2.1 μm outside the range of the present invention.
Baked in the air (1400 ° C)
In Comparative Example 8 in which the IP treatment (1200 ° C., 1800 kg / cm 2 ) was performed, the specific resistance was 0.8 Ω · cm, but 310 pieces / mm.
A pore number of 2 was obtained. In Comparative Example 9 which was an alumina sintered body (raw material purity: 99.8%, average particle diameter: 0.6 μm, fired in air), not only the high specific resistance of 10 14 Ω · cm, but also the number of pores It was 1000 pieces / mm 2 .
【0038】以上表1の実施例1〜4及び比較例1〜9
から明らかなように、本発明は、 平均粒径1μm以下で純度99%以上の高純度酸化チ
タン微粉末を使用すること、 大気中又は還元雰囲気中で1100〜1300℃で焼成(焼
結)すること、 上記焼成を大気中で行う場合、HIP処理(例えば
カ−ボンヒ−タを有するHIP炉でのHIP処理)を必
要とすること、により、はじめて目的とする比抵抗が小
さく、しかも、表面にポア−が極めて少ない酸化チタ
ン、即ち、比抵抗が1.0Ω・cm以下であり、かつ、そ
の表面に存在する3μm径以上のポア−数が1mm2当
たり100個以下である酸化チタン製基板が得られること
が理解でき、また、 上記の還元雰囲気中で焼成(焼結)する場合、続
いてHIP処理を行うことにより、より一層比抵抗及び
ポア−数が改善されること、 上記のHIP処理によってもポア−数が改善され
ること、が理解できる。Examples 1 to 4 and Comparative Examples 1 to 9 shown in Table 1 above.
As is apparent from the above, the present invention uses high-purity titanium oxide fine powder having an average particle diameter of 1 μm or less and a purity of 99% or more, and is fired (sintered) at 1100 to 1300 ° C. in the air or a reducing atmosphere. In the case where the above-mentioned baking is performed in the air, HIP processing (for example, HIP processing in a HIP furnace having a carbon heater) is required. A titanium oxide substrate having very few pores, that is, a titanium oxide substrate having a specific resistance of 1.0 Ω · cm or less and a number of pores having a diameter of 3 μm or more existing on the surface of 100 or less per 1 mm 2 is obtained. In the case of firing (sintering) in the reducing atmosphere, the specific resistance and the number of pores are further improved by performing the HIP treatment. Well - that the number is improved, it can understand.
【0039】[0039]
【発明の効果】本発明は、以上詳記したとおり、「1.0
Ω・cm以下」という極めて小さい比抵抗を有し、しか
も、「3μm径以上のポア−数が100個/1mm2以下」
である酸化チタン製吸着板を用いた基板吸着装置である
ので、この吸着板に対する静電気対策が容易であり、こ
のため静電気の帯電に伴うゴミ等の吸着が生ぜず、しか
も、ポア−が極めて少なく、30μm径以上のポア−が皆
無であることから、ガスなどの吸着なく、このため半導
体ウエハー等の薄板の吸着能、保持能を低下させること
がないなど顕著な効果が生ずる。また、本発明の基板吸
着装置を半導体集積回路の製造装置に組み込まれるウエ
ハハンドやウエハホルダに好適に適用することができ、
半導体の高歩留まり、高集積化などに大きく貢献するこ
とができる。According to the present invention, as described in detail above, "1.0
Ω · cm or less ”and a very small specific resistance, and“ the number of pores with a diameter of 3 μm or more is 100 / mm 2 or less ”.
Since the substrate adsorption device uses a titanium oxide adsorption plate, it is easy to take countermeasures against static electricity on the adsorption plate. Therefore, adsorption of dust and the like due to electrostatic charging does not occur, and the number of pores is extremely small. Since there is no pore having a diameter of 30 .mu.m or more, a remarkable effect is produced such that gas and the like are not adsorbed, and thus the adsorbing ability and holding ability of a thin plate such as a semiconductor wafer are not reduced. Further, the substrate suction apparatus of the present invention can be suitably applied to a wafer hand or a wafer holder incorporated in a semiconductor integrated circuit manufacturing apparatus,
This can greatly contribute to high yield and high integration of semiconductors.
───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) B65G 49/07 H01L 21/68 B25J 15/06 ──────────────────────────────────────────────────続 き Continued on front page (58) Field surveyed (Int.Cl. 7 , DB name) B65G 49/07 H01L 21/68 B25J 15/06
Claims (4)
を備えた基板吸着装置であって、上記吸着板の比抵抗が
1.0Ω・cm以下であり、かつ、その表面に存在する3
μm径以上のポア−数が1mm2当たり100個以下である
酸化チタン製吸着板を備えてなることを特徴とする基板
吸着装置。1. A substrate suction apparatus comprising a suction plate for suction-moving or fixing a thin plate, wherein said suction plate has a specific resistance.
1.0 Ω · cm or less and 3 present on the surface
A substrate adsorption apparatus comprising: a titanium oxide adsorption plate having a number of pores having a diameter of not less than 100 μm per 1 mm 2 .
μm以下で純度99%以上の酸化チタン粉末を成形した
後、1100〜1300℃で大気又は不活性雰囲気中で焼成し、
さらに500kg/cm2以上の圧力下でHIP処理してな
る吸着板を用いることを特徴とする請求項1に記載の基
板吸着装置。2. An adsorption plate made of titanium oxide having an average particle size of 1
After molding a titanium oxide powder having a purity of 99% or less at μm or less, firing at 1100 to 1300 ° C. in air or an inert atmosphere,
2. The substrate suction device according to claim 1, further comprising a suction plate subjected to HIP processing under a pressure of 500 kg / cm 2 or more.
μm以下で純度99%以上の酸化チタン粉末を成形した
後、1100〜1300℃で還元雰囲気中で焼成してなる吸着板
を用いることを特徴とする請求項1に記載の基板吸着装
置。3. An adsorption plate made of titanium oxide having an average particle size of 1
2. The substrate adsorption apparatus according to claim 1, wherein an adsorbing plate formed by molding a titanium oxide powder having a purity of 99% or less with a particle size of not more than [mu] m and firing at 1100 to 1300 [deg.] C. in a reducing atmosphere is used.
μm以下で純度99%以上の酸化チタン粉末を成形した
後、1100〜1300℃で還元雰囲気中で焼成し、さらに500
kg/cm2以上の圧力下でHIP処理してなる吸着板
を用いることを特徴とする請求項1に記載の基板吸着装
置。4. An adsorption plate made of titanium oxide having an average particle size of 1
After forming a titanium oxide powder having a purity of 99% or more with a particle size of less than μm, it is fired in a reducing atmosphere at 1100 to 1300 ° C.
2. The substrate suction device according to claim 1, wherein a suction plate obtained by HIP processing under a pressure of not less than kg / cm 2 is used.
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15877492A JP3171664B2 (en) | 1992-05-26 | 1992-05-26 | Substrate suction device |
| EP19930902556 EP0673023B1 (en) | 1992-05-26 | 1993-02-02 | Vacuum-clamping device using ceramic vacuum-clamping board |
| PCT/JP1993/000120 WO1993024925A1 (en) | 1992-05-26 | 1993-02-02 | Ceramic substrate and its manufacture, and substrate vacuum-clamping device using ceramic vacuum-clamping board |
| DE69325034T DE69325034T2 (en) | 1992-05-26 | 1993-02-02 | VACUUM-HOLDING DEVICE FOR SUBSTRATES WITH CERAMIC VACUUM PLATE |
| KR1019940703996A KR0155186B1 (en) | 1992-05-26 | 1993-02-02 | Ceramic substrate and its manufacture, and substrate vacuum clamping device using ceramic vacuum-clamping board |
| US08/343,464 US5834106A (en) | 1992-05-26 | 1993-02-02 | Ceramic substrate and producing process thereof, and a suction carrier for wafers using a ceramic wafer-chucking substrate |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15877492A JP3171664B2 (en) | 1992-05-26 | 1992-05-26 | Substrate suction device |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05330648A JPH05330648A (en) | 1993-12-14 |
| JP3171664B2 true JP3171664B2 (en) | 2001-05-28 |
Family
ID=15679051
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15877492A Expired - Lifetime JP3171664B2 (en) | 1992-05-26 | 1992-05-26 | Substrate suction device |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3171664B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6716703B2 (en) | 1999-07-29 | 2004-04-06 | Fujitsu Limited | Method of making semiconductor memory device having sources connected to source lines |
-
1992
- 1992-05-26 JP JP15877492A patent/JP3171664B2/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6716703B2 (en) | 1999-07-29 | 2004-04-06 | Fujitsu Limited | Method of making semiconductor memory device having sources connected to source lines |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH05330648A (en) | 1993-12-14 |
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