JP2004128456A - Drying treatment equipment and drying treatment method - Google Patents

Drying treatment equipment and drying treatment method Download PDF

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Publication number
JP2004128456A
JP2004128456A JP2003158498A JP2003158498A JP2004128456A JP 2004128456 A JP2004128456 A JP 2004128456A JP 2003158498 A JP2003158498 A JP 2003158498A JP 2003158498 A JP2003158498 A JP 2003158498A JP 2004128456 A JP2004128456 A JP 2004128456A
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Japan
Prior art keywords
solvent
drying
supercritical drying
vapor pressure
wet
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JP2003158498A
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JP4293596B2 (en
Inventor
Masahiro Yamagata
山形 昌弘
Hisanori Oshiba
大柴 久典
Takatsugu Furuichi
古市 考次
Ryuji Kitakado
北門 龍治
Ikuo Mizobata
溝端 一国雄
Takashi Miyake
三宅 孝志
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Kobe Steel Ltd
Dainippon Screen Manufacturing Co Ltd
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Kobe Steel Ltd
Dainippon Screen Manufacturing Co Ltd
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  • Cleaning Or Drying Semiconductors (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide drying treatment equipment and a drying treatment method capable of preventing a wet treated material from being dried without putting this material in a vessel to dip it in a solvent in storing the material in a supercritical drying device and reducing the amount of the solvent. <P>SOLUTION: In drying treatment equipment that is provided with at least one supercritical drying device storing the wet treated material inside to perform supercritical drying, and the material is conveyed to the supercritical drying device in such a state that the wet treated material is wet by a solvent that is used for the wet treatment. There is provided a vapor pressure adjusting device reducing the amount of evaporation of this solvent to avoid the solvent evaporation that causes the material to be dried, while the material is conveyed to the supercritical drying device after the wet treatment. <P>COPYRIGHT: (C)2004,JPO

Description

【0001】
【発明の属する技術分野】
本発明は、湿式処理された材料を乾燥させることなく超臨界乾燥装置に収納し、その後、超臨界乾燥を行う乾燥処理設備とその乾燥処理方法に関する。
【0002】
【従来の技術】
従来より半導体デバイスを製造する製造過程において、ウェハ等の材料が用いられており、このウェハはエッチング、成膜、現像などの湿式処理を経て超臨界乾燥装置に搬送され、この超臨界乾燥装置で超臨界乾燥が行われている。
一般的に、ウェハ等を超臨界乾燥する超臨界乾燥装置及び超臨界乾燥方法は、特開2002−33302号公報に示されるような超臨界乾燥装置及び方法が採用されている。
【0003】
この超臨界乾燥装置では、湿式処理されたウェハのレジスト破壊又は微細構造の破壊を防止するために、このウェハを小容器内の溶媒に浸漬した状態で、超臨界乾燥装置内に収納し、この超臨界乾燥装置で超臨界乾燥をするようになっている。
また、このウェハを超臨界乾燥装置によって乾燥する場合は、ウェハを複数の小容器内に入れて溶媒に浸した状態で、超臨界乾燥を行っている。
【0004】
【発明が解決しようとする課題】
しかしながら、従来のような特開2002−33302号の超臨界乾燥装置では、ウェハを溶媒に浸しているので、湿式処理されたウェハが超臨界乾燥装置の内部に収納されるまでに、ウェハが乾燥してレジスト破壊、又は、微細構造の破壊することがなく、この点については有効であるが、ウェハ一枚ごとにウェハを小容器に入れ溶媒に浸しているので、ウェハの枚数(数量)が増加すると結果的に溶媒量が多量になる問題があった。
【0005】
また、超臨界乾燥時においても、ウェハを複数の小容器に入れて溶媒に浸したた状態で超臨界乾燥を行っているので、乾燥させる溶媒量が多くなり、乾燥時間が長くなるという問題があった。
そこで、本発明は、上記問題点に鑑み、湿式処理された材料を超臨界乾燥装置に収納する際に、この材料を容器に入れて溶媒に浸さなくても材料の乾燥を防ぐと共に、溶媒量を少なくすることのできる乾燥処理設備及び乾燥処理方法を提供することを目的とする。
【0006】
【課題を解決するための手段】
本発明では、上記の目的を達成するために、次の解決手段を採用した。すなわち、湿式処理された材料を内部に収納して超臨界乾燥を行う少なくとも1基の超臨界乾燥装置を備え、湿式処理された材料が湿式処理で用いられた溶媒によって濡らされた状態で、超臨界乾燥装置に搬送される乾燥処理設備において、材料が超臨界乾燥装置に搬送される間に、溶媒が蒸発して材料が乾燥しないように、この溶媒の蒸発量を低減する蒸気圧調整装置が設けられたことを特徴としている。
【0007】
本発明によれば、溶媒の蒸発量を低減する蒸気圧調整装置が設けられているので、従来のように材料を容器に入れて溶媒に浸した状態で超臨界乾燥装置に収納する必要はなく、材料を容器に入れて溶媒に浸さない分だけ溶媒の量を低減することが可能である。
さらに、溶媒の蒸発量を低減することができるので、材料のレジスト破壊、又は、微細構造の破壊を防止することができる。
また、前記蒸気圧調整装置は、前記材料を取り囲む雰囲気に含まれる溶媒の蒸気圧を飽和蒸気圧の近傍にする装置であることが好ましい。
【0008】
これによれば、材料を取り囲む雰囲気に含まれる溶媒の蒸気圧が飽和蒸気圧となるので、材料を取り囲む雰囲気下で、溶媒は蒸発しにくくなり、その結果、溶媒の蒸発量を抑えることができる。
また、前記蒸気圧調整装置は、前記材料を取り囲む雰囲気の湿度を上昇させる加湿装置であることが好ましい。
これによれば、材料を取り囲む雰囲気の水蒸気圧が飽和蒸気圧に近傍になるので、湿式処理で用いられた溶媒が水溶液である場合には、溶媒は蒸発しにくくなるので溶媒の蒸発を低減することができる。
【0009】
また、湿式処理で用いられた溶媒で濡らされている材料を超臨界乾燥装置内に収納して、この材料に残された溶媒と同一組成の液体と、超臨界乾燥で用いられる流体とを混合した混合流体を超臨界乾燥装置内に供給して、超臨界乾燥装置内の圧力を昇圧させて後、超臨界乾燥を行うことが好ましい。
これによれば、超臨界乾燥装置を昇圧する昇圧過程において、溶媒と同一組成の液体を供給しているので、材料に残されている溶媒の乾燥を防止、又は、低減することができる。
【0010】
また、このような超臨界乾燥装置を昇圧する昇圧過程において、この材料に残された溶媒と同一組成の液体と、超臨界乾燥で用いられる流体とを超臨界乾燥装置内に同時に供給して、超臨界乾燥装置内の圧力を昇圧させた後、超臨界乾燥を行ってもよい。
【0011】
【発明の実施の形態】
以下、図を参照して本発明に係る乾燥処理設備と、乾燥処理方法の実施の形態について説明する。
この乾燥処理設備1は、例えば、半導体デバイスの材料であるウェハ等の製造処理過程で用いられている。
図1に示すように、この乾燥処理設備1はクリンルーム内に配置され、湿式処理されたウェハを内部に収納して超臨界乾燥を行う超臨界乾燥装置2と、湿式処理されたウェハを超臨界乾燥装置2に搬送する搬送装置3と、蒸気圧調整装置4とを備えている。
【0012】
乾燥処理設備1は、クリンルーム内に配置される筐体5に納められており、この筐体5内にはウェハを湿式処理する湿式処理装置6と、カセットステーション7とが設けられており、カセットステーション7は隔壁5Aで区画されている。湿式処理装置6は、現像機、エッチング装置、洗浄装置、コータ、ゲル化装置、リンス装置等種々の液処理装置が採用される。そのため、湿式処理装置6の種類によって湿式処理に使用される溶媒が異なるので、湿式処理されたウェハは湿式処理装置の形態に伴った溶媒によって濡らされることになる。
【0013】
蒸気圧調整装置4は、筐体5内に隣接しており、筐体5内の蒸気圧を飽和蒸気圧の近傍にしたり、又は、筐体5内の蒸気圧を一定に調整する装置である。
また、カセットステーション7には、カセット7a、7b、7cが載置可能な例が示されているが、通常必要に応じて1〜4個のカセットが搬送装置3によってハンドリングされるようになっている。
図1に示すように、搬送装置3は、第1ハンド8と、第2ハンド9とを有しており、第1ハンド8は湿潤搬送用、第2ハンド9は乾燥搬送用である。第1ハンド8はウェハが濡れた状態、すなわち図1の例では、湿式処理装置6から超臨界乾燥装置2への搬送に使用される。第2ハンド9はウェハが乾いた状態、すなわち図1の例では、カセットステーション7から湿式処理装置6への間および超臨界乾燥装置2からカセットステーション7への搬送に使用される。こうすることにより、超臨界乾燥完了後の乾いた状態のウェハの搬送を、水分による汚染のおそれが全くない状態で安定してカセットステーション7に戻すことができる。
【0014】
図1に示した第1ハンド8及び第2ハンド9は縦軸廻りに回動(旋回)可能としたアームを備え、このアームを伸縮自在にするとともに、アーム先端のウェハ支え部を首振り自在にしたスカラー型搬送ロボットで構成することが可能であるが勿論この構成に特定されるものではない。また、搬送装置3は一つのハンド(搬送体)でもよいが、二つ以上のハンドを持つことが好ましい。
次に、カセットステーション7にあるウェハを湿式処理装置6で湿式処理した後、超臨界乾燥装置2内にこのウェハを搬送する過程と、この搬送過程においてウェハを乾燥させない方法について説明する。
【0015】
まず、搬送装置3はカセットステーション7に置かれた処理すべきウェハを取出し、湿式処理装置6に搬送する。
湿式処理装置6が現像機である場合には、アルカリ性水溶液をウェハ面にて滴下して現像を行う。通常現像に要する時間は45秒〜1分程度である。所定時間現像液で現像した後、純水リンスが行われる。リンス工程に要する時間も現像と同程度である。なお、湿式処理装置6が現像機の場合において、ウェハは純水リンス工程後、乾燥処理装置2に搬送されるようになっており、純水で構成された純水リンスは本発明の溶媒に相当する。
【0016】
このリンス工程過程後のウェハは、純水リンス液(溶媒)によって濡らされた状態となっており、この状態で、ウェハは搬送装置3によって湿式処理装置6から取り出され、超臨界乾燥装置2に搬送される。ウェハが湿式処理装置6から超臨界乾燥装置2に搬送される間において、ウェハはウェハを取り囲む雰囲気(筐体5内の雰囲気)に晒されることになるので、これにより溶媒によって濡らされたウェハが自然乾燥してしてしまい、ウェハの微細構造部が毛管力によって倒壊する恐れがあるので、本発明では、湿式処理装置6から超臨界乾燥装置2への搬送は速やかに行うと共に、搬送過程の振動、傾き、稼働や停止時の加速度などでウェハの溶媒がこぼれないようになっている。
【0017】
一方で、筐体5内が、室温22℃、湿度40%前後に保たれている場合においてウェハが筐体5内の雰囲気に晒されると、ウェハに残された溶媒である純水は、純水表面上の空気の自然対流により10秒間で約0.4μm厚ほど乾燥する。筐体5内で換気等が行われ強制対流がある場合には、さらに乾燥の厚みが増加する。これは、0.1μm以下のパターン寸法で高さ及び幅で定義されるアスペクト比が3程度のレジストの場合には、ウェハのパターン間に存在する溶媒が完全に乾燥する量であるため、本発明では、ウェハが湿式処理装置6から超臨界乾燥装置2に搬送される間、蒸気圧調整装置4によってウェハに残された溶媒が蒸発して乾燥しないようにしている。
【0018】
この蒸気圧調整装置4は、筐体5内に含まれる溶媒の蒸気圧を飽和蒸気圧の近傍にする装置である。また、溶媒が純水又は水溶液である場合には、蒸気圧調整装置4は、筐体5内の湿度を上昇させる加湿装置が採用される。
即ち、上記実施の形態では、溶媒が純水で構成されているので、筐体5内は加湿装置(蒸気圧調整装置4)によって加湿され、筐体5内の湿度は高くなる(筐体5内の水蒸気圧は上昇する)。
これにより、ウェハが湿式処理装置6から超臨界乾燥装置2に搬送される間、ウェハが筐体5内の雰囲気に晒されても溶媒は蒸発しにくくなり、蒸発量は低減されウェハは乾燥しない。
【0019】
したがって、湿式処理されたウェハを容器にいれて溶媒に浸さなくても、ウェハの乾燥を防ぐことができる。さらに、筐体5内に含まれる溶媒の蒸気圧を蒸気圧調整装置4によって飽和蒸気圧の近傍に一定に調整することができるので、この雰囲気下ではウェハは乾燥することがなくなる。
なお、この蒸気圧調整装置4は、筐体5に隣接してもよいし、筐体5内、或いは、複数の筐体5の共通装置として設置してもよい。
また、筐体5内のウェハを取り囲む雰囲気の適切な湿度は、搬送時にウェハ等が雰囲気接触している時間に依存するが、少なくとも、70%以上、好ましくは、80%以上に保つことにより、0.1μm以下のウェハ等の自然乾燥を低減、又は防止してウェハの破壊なしに搬送が可能になる。
【0020】
また、筐体5内の雰囲気を超臨界乾燥装置2内に入るようにして、超臨界乾燥装置2内の溶媒の蒸気圧を間接的に蒸気圧調整装置4によって飽和蒸気圧に近づけると、より効果的である。
また、上記実施の形態では、湿式処理装置6と超臨界乾燥装置2とを含めた筐体5内全体の雰囲気に対して、この雰囲気に含まれる溶媒の蒸気圧を飽和蒸気圧近傍まで上昇させる例を示したが、ウェハが設置、又は、搬送される場所の雰囲気のみに対して、溶媒の水蒸気圧を飽和蒸気圧の近傍まで上昇させるようにしてもよい。例えば、図2に示すように、ウェハが湿式処理装置6から超臨界乾燥装置2まで搬送される搬送ルート10を筐体5Bで区画して、この区画された筐体5B内の雰囲気に含まれる溶媒の蒸気圧を蒸気圧調整装置4によって飽和蒸気圧近傍まで上昇させるようにするのが好ましい。このようにすれば、筐体5B内の体積が筐体5よりも小さいので、この筐体5B内の溶媒の蒸気圧を飽和蒸気圧にするために必要な溶媒量を少なくすることができる。なお、図2においてカセットステーション7は省略しており、湿式処理されたウェハは筐体5B内において、湿式処理装置6から超臨界乾燥装置2へ移動するようになっており、蒸気圧調整装置4は筐体5Bに隣接している。
【0021】
次に、超臨界乾燥装置2に濡れた状態で搬送されたウェハを超臨界乾燥装置2で乾燥する方法について説明する。超臨界乾燥装置2では、超臨界流体が用いられ、超臨界流体として、通常、二酸化炭素の流体が使用される。
この超臨界流体は、図3に示すように、気体と液体とが共存できる限界の温度及び圧力(臨界点)を越えた状態にあり、毛管力が略零である流体である。
この超臨界乾燥装置2でウェハを超臨界乾燥をするには、ウェハを超臨界乾燥装置2内に収納した状態で、超臨界乾燥装置2内を二酸化炭素で昇圧して、この超臨界乾燥装置2内を超臨界乾燥条件(例えば50℃、10MPa)にしなければならないが、超臨界乾燥装置2内が超臨界乾燥条件になる前(超臨界乾燥装置2内を昇圧する昇圧過程)では、昇圧している二酸化炭素の流体と、ウェハにある溶媒との間に界面が存在するため、この溶媒が二酸化炭素に溶解してウェハが乾燥し、ウェハのレジスト破壊、又は、微細構造の破壊が発生する恐れがある。特に低圧(3〜4MPa程度)では、二酸化炭素中への溶媒の溶解度が高い場合が多いため、昇圧に時間がかかると乾燥が進行し、レジスト倒壊の危険性が大である。
【0022】
そこで本発明では、超臨界乾燥装置2内を昇圧する昇圧過程において、昇圧過程に使用する二酸化炭素ガス、又は、二酸化炭素液等の流体と、湿式処理後のウェハ上に残された溶媒と同じ組成の液体、又は、気体とを混ぜた混合流体で、超臨界乾燥装置2内が超臨界乾燥条件になるまで超臨界乾燥装置2内を昇圧する。このようにすれば、昇圧過程において、溶媒の混合流体に溶解する速度が遅くなると共に、溶媒の混合流体への溶解量が減少するので、ウェハの乾燥を防止、或いは、低減することができる。なお、この場合において、昇圧過程に使用する二酸化炭素ガス、又は、二酸化炭素液等の流体と、湿式処理後のウェハ上に残された溶媒と同じ組成の液体、又は、気体とを、超臨界乾燥装置2内に同時に供給するようにしてもよい。
【0023】
そして、上記の方法により超臨界乾燥装置2内を超臨界乾燥条件にすれば、ウェハのレジストパターン間にある溶媒と超臨界二酸化炭素が一相状態になり、気液界面が存在しないため、界面張力等によって、ウェハのレジスト倒壊、又は、微細構造の破壊を起こすことがない。その後、圧力を減じて超臨界状態から気体状態に変化させれば、気液平衝線を横切ることなく界面張力フリーでウェハを乾燥させることができる。
なお、二酸化炭素と溶媒との同時供給の場合は、超臨界処理条件になる前に液供給を停止し、二酸化炭素のみで昇圧することも可能である。
【0024】
また、昇圧過程においてウェハの溶媒の乾燥を防止する方法として、ウェハ表面上に溶媒を滴下しながら二酸化炭素のみで昇圧することも可能である。この場合においては、二酸化炭素に溶解する量以上の溶媒を供給しないとウェハが乾燥することになるので、溶媒量が増えて昇圧終了後の乾燥時の負担が増加し、処理時間が長くなる。このため、溶媒を十分に二酸化炭素へ溶解させた二酸化炭素(溶媒の二酸化炭素に対する溶解度が飽和溶解度になった状態の二酸化炭素)を用いて昇圧するのが最も効率的である。
【0025】
なお、図1では搬送装置3として定置式(旋回式)のものが例示されているが、状況に応じて移動式(走行式)の搬送装置3が用いられる場合もある。また、図1におけるカセットステーション7に付随して第二の搬送装置3が配置されることもある。この場合、第二の搬送装置はカセットからのウェハの出し入れを司り、第一の搬送装置との間でウェハの受け渡しを行うこととなる。
また、ウェハを湿式処理する湿式処理装置3が乾燥処理設備1と一体化されていてもよい。
【0026】
本発明の実施の形態は以上の通りであるが、その趣旨の範囲内で種々の改変が可能である。
図1では湿式処理装置6や超臨界乾燥装置2がそれぞれ1基で示されているが、必要に応じて複数個の湿式処理装置6や超臨界乾燥装置2を配置することは当然の選択である。また、湿式処理装置6と超臨界乾燥装置2に加えて、ベイク炉や置換装置が組み込まれる場合もある。
また、上記の実施の形態では、搬送装置3によって湿式処理されたウェハが搬送されるようになっているが、この乾燥処理設備1は必ずしもウェハを搬送する搬送装置を有していなくてもよい。例えば、湿式処理されたウェハが人為的に運ばれて、このウェハが湿式処理で用いられた溶媒によって濡らされた状態で、超臨界乾燥装置2に搬送されるものであってもよい。
【0027】
また、上記の実施の形態では、湿式処理で濡らされたウェハの溶媒は純水で構成された純水リンス液とされていたが、これに限られず、湿式処理装置の種類によって溶媒は適宜に変更される。例えば、この溶媒には水や、ハイドロフロロエーテル、フロリナート(登録商標、スリーエム社)などのフルオロカーボン系溶液や、テロメリックアルコールなどのアルコール系溶液、又は、その他の有機溶媒が考えられる。
溶媒として有機溶媒(例えばフルオロカーボン系溶液)が使用され、ウェハが有機溶媒で濡れている場合、この有機溶媒と同じ液体が蒸発して発生した蒸気を用いて筐体5、5B内を飽和蒸気圧に近づければ良い。なお、有機溶媒を蒸発させてその蒸気を得る場合、蒸気圧調整装置4には有機溶媒を加熱して蒸発させる蒸気圧発生装置、若しくは有機溶媒に超音波を付与して蒸発させる蒸気圧発生装置を用いれば良い。
【0028】
【発明の効果】
本発明によれば、湿式処理されたウェハを取り囲む雰囲気に含まれる溶媒の蒸気圧を蒸気圧調整装置によって飽和蒸気圧の近傍にし、この雰囲気下でウェハを搬送、又は、処理しているので、ウェハのレジスト破壊、又は、微細構造の破壊を防ぐと共に、溶媒の量を低減することができる。
【図面の簡単な説明】
【図1】本発明の実施の形態にかかる乾燥処理設備を半導体の材料となるウェハの製造設備に配置した配置図である。
【図2】同ウェハの搬送ルートを筐体で区画した形態を示す配置図である。
【図3】圧力と温度の状態図である。
【符号の説明】
1 乾燥処理設備
2 超臨界乾燥装置
3 搬送装置
4 蒸気圧調整装置
5 筐体
6 湿式処理装置
7 カセットステーション
8 第一ハンド
9 第二ハンド
[0001]
TECHNICAL FIELD OF THE INVENTION
TECHNICAL FIELD The present invention relates to a drying treatment facility for storing a wet-processed material in a supercritical drying apparatus without drying the material and thereafter performing supercritical drying, and a drying treatment method therefor.
[0002]
[Prior art]
Conventionally, in the manufacturing process of manufacturing semiconductor devices, materials such as wafers have been used, and the wafers are transported to a supercritical drying apparatus through wet processing such as etching, film formation, and development. Supercritical drying is being performed.
Generally, as a supercritical drying apparatus and a supercritical drying method for supercritically drying a wafer or the like, a supercritical drying apparatus and a method as disclosed in JP-A-2002-33302 are adopted.
[0003]
In this supercritical drying apparatus, this wafer is stored in a supercritical drying apparatus while being immersed in a solvent in a small container in order to prevent resist destruction or microstructural destruction of the wet-processed wafer. Supercritical drying is performed by a supercritical drying device.
When the wafer is dried by a supercritical drying apparatus, the supercritical drying is performed while the wafer is placed in a plurality of small containers and immersed in a solvent.
[0004]
[Problems to be solved by the invention]
However, in the conventional supercritical drying apparatus disclosed in JP-A-2002-33302, since the wafer is immersed in the solvent, the wafer is dried before the wet-processed wafer is stored in the supercritical drying apparatus. It is effective in this respect without destroying the resist or destroying the fine structure. However, since each wafer is immersed in a solvent in a small container, the number of wafers (quantity) is reduced. When the amount is increased, the amount of the solvent becomes large as a result.
[0005]
Also, during supercritical drying, since the supercritical drying is performed in a state where the wafer is immersed in a solvent in a plurality of small containers, the amount of solvent to be dried increases, and the drying time becomes longer. there were.
Accordingly, the present invention has been made in view of the above-described problems, and when storing a wet-processed material in a supercritical drying apparatus, it is possible to prevent the material from drying without putting the material in a container and immersing the material in a solvent. It is an object of the present invention to provide a drying treatment facility and a drying treatment method capable of reducing the amount of drying.
[0006]
[Means for Solving the Problems]
The present invention employs the following solution in order to achieve the above object. That is, the apparatus includes at least one supercritical drying device that stores therein the wet-processed material and performs supercritical drying, and the wet-processed material is wetted by the solvent used in the wet process. In the drying processing equipment transported to the critical drying device, while the material is transported to the supercritical drying device, so that the solvent does not evaporate and the material is not dried, a vapor pressure adjusting device that reduces the amount of evaporation of the solvent is provided. It is characterized by being provided.
[0007]
According to the present invention, since the vapor pressure adjusting device for reducing the amount of evaporation of the solvent is provided, it is not necessary to put the material in a container and immerse the solvent in the supercritical drying device as in the related art. In addition, it is possible to reduce the amount of the solvent by an amount that does not allow the material to be put in the container and soaked in the solvent.
Further, since the evaporation amount of the solvent can be reduced, it is possible to prevent the resist from being destroyed in the material or the fine structure from being destroyed.
Further, it is preferable that the vapor pressure adjusting device is a device that makes a vapor pressure of a solvent contained in an atmosphere surrounding the material close to a saturated vapor pressure.
[0008]
According to this, since the vapor pressure of the solvent contained in the atmosphere surrounding the material becomes the saturated vapor pressure, the solvent is less likely to evaporate under the atmosphere surrounding the material, and as a result, the amount of evaporation of the solvent can be suppressed. .
Further, it is preferable that the vapor pressure adjusting device is a humidifying device that increases the humidity of an atmosphere surrounding the material.
According to this, since the water vapor pressure of the atmosphere surrounding the material becomes close to the saturated vapor pressure, when the solvent used in the wet processing is an aqueous solution, the solvent is less likely to evaporate, so that the evaporation of the solvent is reduced. be able to.
[0009]
In addition, the material wetted with the solvent used in the wet processing is stored in the supercritical drying apparatus, and a liquid having the same composition as the solvent remaining in the material is mixed with the fluid used in the supercritical drying. It is preferable that the mixed fluid is supplied into a supercritical drying apparatus, the pressure in the supercritical drying apparatus is increased, and then the supercritical drying is performed.
According to this, since the liquid having the same composition as the solvent is supplied in the pressurizing process of increasing the pressure of the supercritical drying apparatus, it is possible to prevent or reduce the drying of the solvent remaining in the material.
[0010]
Further, in the pressure increasing process of increasing the pressure of the supercritical drying device, a liquid having the same composition as the solvent left in the material and a fluid used in the supercritical drying are simultaneously supplied into the supercritical drying device, After increasing the pressure in the supercritical drying apparatus, supercritical drying may be performed.
[0011]
BEST MODE FOR CARRYING OUT THE INVENTION
Hereinafter, an embodiment of a drying treatment facility and a drying treatment method according to the present invention will be described with reference to the drawings.
The drying processing equipment 1 is used, for example, in a manufacturing process of a wafer or the like which is a material of a semiconductor device.
As shown in FIG. 1, the drying processing equipment 1 is disposed in a clean room, and stores a wet-processed wafer therein and performs supercritical drying. A transport device 3 for transporting to the critical drying device 2 and a vapor pressure adjusting device 4 are provided.
[0012]
The drying processing equipment 1 is housed in a housing 5 arranged in a clean room, and a wet processing device 6 for performing wet processing on a wafer and a cassette station 7 are provided in the housing 5. The cassette station 7 is partitioned by a partition 5A. As the wet processing apparatus 6, various liquid processing apparatuses such as a developing machine, an etching apparatus, a cleaning apparatus, a coater, a gelling apparatus, and a rinsing apparatus are employed. Therefore, the solvent used for the wet processing differs depending on the type of the wet processing apparatus 6, so that the wafer that has been subjected to the wet processing is wet by the solvent according to the form of the wet processing apparatus.
[0013]
The steam pressure adjusting device 4 is adjacent to the inside of the housing 5 and is a device that adjusts the steam pressure in the housing 5 to near the saturated steam pressure, or adjusts the steam pressure in the housing 5 to be constant. .
Although an example in which cassettes 7a, 7b, and 7c can be placed in the cassette station 7 is shown, one to four cassettes are usually handled by the transport device 3 as needed. I have.
As shown in FIG. 1, the transport device 3 has a first hand 8 and a second hand 9, wherein the first hand 8 is for wet transport and the second hand 9 is for dry transport. The first hand 8 is used when the wafer is wet, that is, in the example of FIG. 1, the wafer is transferred from the wet processing apparatus 6 to the supercritical drying apparatus 2. The second hand 9 is used when the wafer is in a dry state, that is, in the example of FIG. 1, between the cassette station 7 and the wet processing apparatus 6 and from the supercritical drying apparatus 2 to the cassette station 7. This makes it possible to stably return the wafer in a dry state after the completion of the supercritical drying to the cassette station 7 without any risk of contamination by moisture.
[0014]
Each of the first hand 8 and the second hand 9 shown in FIG. 1 has an arm which can be turned (turned) around a vertical axis, and this arm can be extended and contracted, and the wafer support at the tip of the arm can be swung. Although it is possible to configure the scalar type transfer robot described above, it is needless to say that the present invention is not limited to this configuration. Further, the transport device 3 may be a single hand (transport body), but preferably has two or more hands.
Next, a description will be given of a process in which the wafer in the cassette station 7 is wet-processed by the wet processing device 6 and then transferred to the supercritical drying device 2 and a method of not drying the wafer in the transfer process.
[0015]
First, the transfer device 3 takes out a wafer to be processed placed in the cassette station 7 and transfers it to the wet processing device 6.
When the wet processing apparatus 6 is a developing machine, development is performed by dropping an alkaline aqueous solution on the wafer surface. Usually, the time required for development is about 45 seconds to 1 minute. After developing with a developer for a predetermined time, pure water rinsing is performed. The time required for the rinsing step is about the same as that for development. When the wet processing apparatus 6 is a developing machine, the wafer is transferred to the drying processing apparatus 2 after the pure water rinsing step, and the pure water rinse composed of pure water is used as the solvent of the present invention. Equivalent to.
[0016]
The wafer after the rinsing step is in a state of being wet with a pure water rinsing liquid (solvent). In this state, the wafer is taken out of the wet processing apparatus 6 by the transfer device 3 and transferred to the supercritical drying device 2. Conveyed. While the wafer is transferred from the wet processing apparatus 6 to the supercritical drying apparatus 2, the wafer is exposed to the atmosphere surrounding the wafer (the atmosphere in the housing 5). In the present invention, since the wafer is naturally dried and the microstructure portion of the wafer may collapse due to the capillary force, the transfer from the wet processing apparatus 6 to the supercritical drying apparatus 2 is performed promptly and the transfer process is performed. The solvent of the wafer is prevented from spilling due to vibration, tilt, acceleration during operation or stop, and the like.
[0017]
On the other hand, when the wafer is exposed to the atmosphere in the housing 5 when the inside of the housing 5 is maintained at a room temperature of 22 ° C. and a humidity of about 40%, pure water as a solvent remaining on the wafer becomes pure water. Dry by about 0.4 μm thickness in 10 seconds by natural convection of air on the water surface. When ventilation or the like is performed in the housing 5 and forced convection occurs, the thickness of drying further increases. In the case of a resist having a pattern dimension of 0.1 μm or less and an aspect ratio defined by height and width of about 3, the solvent existing between the patterns on the wafer is completely dried. In the present invention, while the wafer is transferred from the wet processing apparatus 6 to the supercritical drying apparatus 2, the solvent left on the wafer by the vapor pressure adjusting device 4 is prevented from evaporating and drying.
[0018]
This vapor pressure adjusting device 4 is a device that makes the vapor pressure of the solvent contained in the housing 5 close to the saturated vapor pressure. When the solvent is pure water or an aqueous solution, a humidifying device that increases the humidity in the housing 5 is used as the vapor pressure adjusting device 4.
That is, in the above embodiment, since the solvent is composed of pure water, the inside of the housing 5 is humidified by the humidifying device (the vapor pressure adjusting device 4), and the humidity in the housing 5 is increased (the housing 5 The internal water vapor pressure rises).
Thus, while the wafer is transferred from the wet processing apparatus 6 to the supercritical drying apparatus 2, the solvent is less likely to evaporate even if the wafer is exposed to the atmosphere in the housing 5, the evaporation amount is reduced, and the wafer does not dry. .
[0019]
Therefore, it is possible to prevent the wafer from drying even if the wet-processed wafer is not put in a container and immersed in the solvent. Further, since the vapor pressure of the solvent contained in the housing 5 can be adjusted to be constant near the saturated vapor pressure by the vapor pressure adjusting device 4, the wafer does not dry under this atmosphere.
The vapor pressure adjusting device 4 may be adjacent to the housing 5 or may be installed in the housing 5 or as a common device of the plurality of housings 5.
Further, the appropriate humidity of the atmosphere surrounding the wafer in the housing 5 depends on the time during which the wafer or the like is in contact with the atmosphere during transfer, but by maintaining at least 70% or more, preferably 80% or more, Natural drying of a wafer of 0.1 μm or less can be reduced or prevented, and the wafer can be transported without breaking.
[0020]
Further, when the atmosphere in the housing 5 is put into the supercritical drying device 2 and the vapor pressure of the solvent in the supercritical drying device 2 is indirectly brought close to the saturated vapor pressure by the vapor pressure adjusting device 4, It is effective.
In the above-described embodiment, the vapor pressure of the solvent contained in the entire atmosphere of the housing 5 including the wet processing apparatus 6 and the supercritical drying apparatus 2 is increased to near the saturated vapor pressure. Although an example has been described, the vapor pressure of the solvent may be increased to near the saturated vapor pressure only in the atmosphere where the wafer is installed or transported. For example, as shown in FIG. 2, a transfer route 10 in which a wafer is transferred from the wet processing apparatus 6 to the supercritical drying apparatus 2 is partitioned by the housing 5B, and is included in the atmosphere in the partitioned housing 5B. It is preferable that the vapor pressure of the solvent be increased to near the saturated vapor pressure by the vapor pressure adjusting device 4. With this configuration, since the volume inside the housing 5B is smaller than that of the housing 5, it is possible to reduce the amount of the solvent necessary for setting the vapor pressure of the solvent in the housing 5B to the saturated vapor pressure. In FIG. 2, the cassette station 7 is omitted, and the wet-processed wafer is moved from the wet processing apparatus 6 to the supercritical drying apparatus 2 in the housing 5B. Is adjacent to the housing 5B.
[0021]
Next, a method of drying the wafer transported in a state of being wet by the supercritical drying device 2 by the supercritical drying device 2 will be described. In the supercritical drying device 2, a supercritical fluid is used, and a carbon dioxide fluid is usually used as the supercritical fluid.
As shown in FIG. 3, this supercritical fluid is a fluid in which the temperature and the pressure (critical point) of the gas and the liquid are beyond the limit and the capillary force is substantially zero.
In order to supercritically dry a wafer with the supercritical drying apparatus 2, the pressure inside the supercritical drying apparatus 2 is increased with carbon dioxide while the wafer is housed in the supercritical drying apparatus 2. 2 must be under supercritical drying conditions (for example, 50 ° C., 10 MPa), but before the inside of the supercritical drying device 2 becomes the supercritical drying condition (the pressurizing process of increasing the pressure inside the supercritical drying device 2), the pressure is increased. Since there is an interface between the carbon dioxide fluid and the solvent on the wafer, this solvent dissolves in the carbon dioxide and dries the wafer, causing resist destruction of the wafer or destruction of the microstructure. There is a risk of doing. In particular, at low pressure (about 3 to 4 MPa), the solubility of the solvent in carbon dioxide is often high, so that if the pressure is increased, drying takes place and the risk of resist collapse is great.
[0022]
Therefore, in the present invention, in the pressurizing step of pressurizing the inside of the supercritical drying apparatus 2, the same fluid as the carbon dioxide gas or the carbon dioxide liquid used in the pressurizing step and the solvent remaining on the wafer after the wet processing are used. The pressure inside the supercritical drying apparatus 2 is increased by using a liquid mixture of a composition or a gas mixed with a gas until the inside of the supercritical drying apparatus 2 reaches a supercritical drying condition. With this configuration, in the pressure increasing process, the rate of dissolution in the mixed fluid of the solvent is reduced, and the amount of the dissolved solvent in the mixed fluid is reduced, so that the drying of the wafer can be prevented or reduced. Note that, in this case, a carbon dioxide gas used in the pressure increasing process, or a fluid such as a carbon dioxide liquid, and a liquid or a gas having the same composition as the solvent remaining on the wafer after the wet processing are supercritical. You may make it supply simultaneously in the drying device 2.
[0023]
If the inside of the supercritical drying apparatus 2 is set to the supercritical drying condition by the above-described method, the solvent and the supercritical carbon dioxide between the resist patterns on the wafer are in a single-phase state, and there is no gas-liquid interface. The resist does not collapse on the wafer or the fine structure is not destroyed by the tension or the like. Thereafter, if the pressure is reduced to change from the supercritical state to the gas state, the wafer can be dried without interfacial tension without crossing the gas-liquid balance line.
In the case of simultaneous supply of carbon dioxide and a solvent, it is also possible to stop the liquid supply before the supercritical processing conditions are reached and to increase the pressure only with carbon dioxide.
[0024]
Further, as a method for preventing the solvent of the wafer from drying in the pressure increasing process, it is also possible to increase the pressure only with carbon dioxide while dropping the solvent on the wafer surface. In this case, unless the solvent is supplied in an amount greater than the amount that dissolves in carbon dioxide, the wafer will dry. Therefore, the amount of the solvent will increase, the load on drying after the end of the pressure increase will increase, and the processing time will increase. For this reason, it is most efficient to increase the pressure using carbon dioxide in which the solvent is sufficiently dissolved in carbon dioxide (carbon dioxide in a state where the solubility of the solvent in carbon dioxide is a saturated solubility).
[0025]
In FIG. 1, a stationary (rotating) transport device is illustrated as the transport device 3, but a mobile (traveling) transport device 3 may be used depending on the situation. Further, the second transfer device 3 may be arranged in association with the cassette station 7 in FIG. In this case, the second transfer device controls the transfer of the wafer from the cassette and transfers the wafer to and from the first transfer device.
Further, the wet processing apparatus 3 for performing wet processing on a wafer may be integrated with the drying processing equipment 1.
[0026]
Although the embodiment of the present invention is as described above, various modifications are possible within the scope of the gist.
In FIG. 1, the wet processing apparatus 6 and the supercritical drying apparatus 2 are each shown as a single unit, but it is a matter of course to arrange a plurality of wet processing apparatuses 6 and the supercritical drying apparatus 2 as necessary. is there. Further, in addition to the wet processing apparatus 6 and the supercritical drying apparatus 2, a baking furnace or a replacement apparatus may be incorporated.
Further, in the above embodiment, the wafer that has been wet-processed is transported by the transport device 3, but the drying processing equipment 1 does not necessarily need to have a transport device that transports the wafer. . For example, a wafer that has been wet-processed may be conveyed artificially and transferred to the supercritical drying apparatus 2 in a state where the wafer is wetted by the solvent used in the wet process.
[0027]
Further, in the above-described embodiment, the solvent of the wafer wetted by the wet processing is a pure water rinsing liquid composed of pure water, but the present invention is not limited to this, and the solvent may be appropriately determined depending on the type of the wet processing apparatus. Be changed. For example, the solvent may be water, a fluorocarbon-based solution such as hydrofluoroether or Fluorinert (registered trademark, 3M), an alcohol-based solution such as telomer alcohol, or another organic solvent.
When an organic solvent (for example, a fluorocarbon-based solution) is used as the solvent and the wafer is wet with the organic solvent, the inside of the casings 5 and 5B is saturated with a saturated vapor pressure using vapor generated by evaporating the same liquid as the organic solvent. It should be close to. When evaporating the organic solvent to obtain its vapor, the vapor pressure adjusting device 4 heats and evaporates the organic solvent, or a vapor pressure generating device that applies ultrasonic waves to the organic solvent to evaporate it. May be used.
[0028]
【The invention's effect】
According to the present invention, the vapor pressure of the solvent contained in the atmosphere surrounding the wet-processed wafer is brought close to the saturated vapor pressure by the vapor pressure adjusting device, and the wafer is transported or processed under this atmosphere. It is possible to prevent the resist destruction of the wafer or the destruction of the fine structure, and to reduce the amount of the solvent.
[Brief description of the drawings]
FIG. 1 is a layout view in which a drying processing facility according to an embodiment of the present invention is disposed in a manufacturing facility for a wafer to be a semiconductor material.
FIG. 2 is a layout view showing a form in which a transfer route of the wafer is divided by a housing.
FIG. 3 is a state diagram of pressure and temperature.
[Explanation of symbols]
REFERENCE SIGNS LIST 1 Drying processing equipment 2 Supercritical drying device 3 Transport device 4 Vapor pressure adjusting device 5 Housing 6 Wet processing device 7 Cassette station 8 First hand 9 Second hand

Claims (10)

湿式処理された材料を内部に収納して超臨界乾燥を行う少なくとも1基の超臨界乾燥装置(2)を備え、湿式処理された材料が湿式処理で用いられた溶媒によって濡らされた状態で、超臨界乾燥装置(2)に搬送される乾燥処理設備において、
前記材料が湿式処理されてから超臨界乾燥装置(2)に搬送される間に、前記溶媒が蒸発して材料が乾燥しないように、この溶媒の蒸発量を低減する蒸気圧調整装置(4)が設けられたことを特徴とする乾燥処理設備。
It is provided with at least one supercritical drying device (2) for storing the wet-processed material therein and performing supercritical drying, wherein the wet-processed material is wetted by the solvent used in the wet process, In the drying processing equipment transported to the supercritical drying device (2),
A vapor pressure adjusting device (4) for reducing the amount of evaporation of the solvent so that the solvent does not evaporate and the material is not dried while the material is wet-processed and then conveyed to a supercritical drying device (2). A drying treatment facility, characterized in that:
前記蒸気圧調整装置(4)は、前記材料を取り囲む雰囲気に含まれる溶媒の蒸気圧を一定の状態に調整する装置であることを特徴とする請求項1に記載の乾燥処理設備。The drying treatment equipment according to claim 1, wherein the vapor pressure adjusting device (4) is a device that adjusts a vapor pressure of a solvent contained in an atmosphere surrounding the material to a constant state. 前記蒸気圧調整装置(4)は、前記材料を取り囲む雰囲気含まれる溶媒の蒸気圧を飽和蒸気圧の近傍にする装置であることを特徴とする請求項1に記載の乾燥処理設備。The drying treatment equipment according to claim 1, wherein the vapor pressure adjusting device (4) is a device for setting a vapor pressure of a solvent contained in an atmosphere surrounding the material to near a saturated vapor pressure. 前記蒸気圧調整装置(4)は、前記材料を取り囲む雰囲気の湿度を上昇させる加湿装置であることを特徴とする請求項1記載の乾燥処理設備。The drying treatment equipment according to claim 1, wherein the vapor pressure adjusting device (4) is a humidifying device for increasing the humidity of an atmosphere surrounding the material. 湿式処理で用いられた溶媒で濡らされている材料を、湿式処理で使用した溶媒の蒸気圧を飽和蒸気圧に近づけた雰囲気下で、搬送、又は、処理することにより、材料に残された溶媒を乾燥させないことを特徴とする乾燥処理方法。Solvent left in the material by transporting or processing the material wetted with the solvent used in the wet processing under an atmosphere in which the vapor pressure of the solvent used in the wet processing is close to the saturated vapor pressure, or A drying process, wherein the drying process is not performed. 前記溶媒は純水又は水で構成されていることを特徴とする請求項5に記載の乾燥処理方法。The drying method according to claim 5, wherein the solvent comprises pure water or water. 材料を取り囲む雰囲気の湿度を70%以上にした状態で、溶媒で濡らされた材料を、搬送、又は、処理することにより、材料に残された溶媒を乾燥させないことを特徴とする乾燥処理方法。A drying method, comprising: transporting or processing a material wetted with a solvent in a state where the humidity of an atmosphere surrounding the material is set to 70% or more, so that a solvent remaining in the material is not dried. 湿式処理で用いられた溶媒で濡らされている材料を超臨界乾燥装置(2)内に収納して、この材料に残された溶媒と同一組成の液体と、超臨界乾燥で用いられる流体とを混合した混合流体を超臨界乾燥装置(2)内に供給して、超臨界乾燥装置(2)内の圧力を昇圧させて後、超臨界乾燥を行うことを特徴とする乾燥処理方法。The material wetted with the solvent used in the wet processing is stored in the supercritical drying device (2), and a liquid having the same composition as the solvent remaining in the material and a fluid used in the supercritical drying are mixed. A drying method comprising supplying a mixed fluid into a supercritical drying device (2), increasing the pressure in the supercritical drying device (2), and then performing supercritical drying. 湿式処理で用いられた溶媒で濡らされた材料を超臨界乾燥装置(2)内に収納して、この材料に残された溶媒と同一組成の液体と、超臨界乾燥で用いられる流体とを超臨界乾燥装置(2)内に同時に供給して、超臨界乾燥装置(2)内の圧力を昇圧させた後、超臨界乾燥を行うことを特徴とする乾燥処理方法。The material wetted with the solvent used in the wet processing is stored in the supercritical drying apparatus (2), and a liquid having the same composition as the solvent remaining in the material and a fluid used in the supercritical drying are superposed. A drying treatment method comprising simultaneously supplying the mixture into a critical drying device (2) to increase the pressure in the supercritical drying device (2), and then performing supercritical drying. 前記溶媒はフルオロカーボン系溶液又はアルコール系溶液で構成されていることを特徴とする請求項5に記載の乾燥処理方法。The drying method according to claim 5, wherein the solvent is a fluorocarbon-based solution or an alcohol-based solution.
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JP2009283853A (en) * 2008-05-26 2009-12-03 Tokyo Electron Ltd Substrate processing apparatus, substrate processing method,program, and storage medium
KR101231309B1 (en) 2008-04-07 2013-02-07 도쿄엘렉트론가부시키가이샤 Substrate treatment apparatus, substrate treatment method and recording medium having program recorded
KR101568469B1 (en) 2012-07-18 2015-11-11 도쿄엘렉트론가부시키가이샤 Substrate processing method, substrate processing apparatus and storage medium

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101231309B1 (en) 2008-04-07 2013-02-07 도쿄엘렉트론가부시키가이샤 Substrate treatment apparatus, substrate treatment method and recording medium having program recorded
JP2009283853A (en) * 2008-05-26 2009-12-03 Tokyo Electron Ltd Substrate processing apparatus, substrate processing method,program, and storage medium
KR101568469B1 (en) 2012-07-18 2015-11-11 도쿄엘렉트론가부시키가이샤 Substrate processing method, substrate processing apparatus and storage medium

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