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JP3075906B2 - Substrate coated with water-soluble salt - Google Patents

Substrate coated with water-soluble salt

Info

Publication number
JP3075906B2
JP3075906B2 JP06021391A JP2139194A JP3075906B2 JP 3075906 B2 JP3075906 B2 JP 3075906B2 JP 06021391 A JP06021391 A JP 06021391A JP 2139194 A JP2139194 A JP 2139194A JP 3075906 B2 JP3075906 B2 JP 3075906B2
Authority
JP
Japan
Prior art keywords
water
glass
substrate
soluble salt
sodium
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 - Fee Related
Application number
JP06021391A
Other languages
Japanese (ja)
Other versions
JPH06340865A (en
Inventor
松本  潔
諭司 竹田
誠 能代
良一 篠
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
AGC Inc
Original Assignee
Asahi Glass Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Asahi Glass Co Ltd filed Critical Asahi Glass Co Ltd
Priority to JP06021391A priority Critical patent/JP3075906B2/en
Publication of JPH06340865A publication Critical patent/JPH06340865A/en
Application granted granted Critical
Publication of JP3075906B2 publication Critical patent/JP3075906B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Cleaning In General (AREA)
  • Prevention Of Fouling (AREA)
  • Surface Treatment Of Glass (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は水溶性塩が塗布された基
体に関する。
The present invention relates to a substrate coated with a water-soluble salt.

【0002】[0002]

【従来の技術】従来、基体の製造、保管、運搬中に表面
に付着する汚染を回避、除去する目的のため、(1)当
該基体の周辺雰囲気を清浄とする、(2)合紙、スペー
サー、保管容器等の当該基体に接触または近傍に存在す
る材料からの汚染物質の転移を防止する、(3)必要な
操作の前に付着した汚染を物理的、化学的作用を有する
洗浄により除去する方法が実施されていた。
2. Description of the Related Art Conventionally, for the purpose of avoiding and removing contamination adhering to a surface during the manufacture, storage and transportation of a substrate, (1) the atmosphere around the substrate is cleaned, (2) interleaf paper and spacers Prevent transfer of contaminants from materials in contact with or in the vicinity of the substrate, such as a storage container, and (3) remove contaminants adhered before necessary operations by washing having physical and chemical actions. The method was being implemented.

【0003】[0003]

【発明が解決しようとする課題】最近の材料科学の発展
により、材料の表面に高い清浄性が求められる場合が多
くなり、きわめて少量の汚染の存在が問題となる。例え
ば清浄なガラス表面を必要とする分野で忌避される「撥
水性」は表面に吸着したきわめて少量の有機物により発
現する。
With the recent development of material science, high cleanliness is often required on the surface of a material, and the presence of a very small amount of contamination becomes a problem. For example, "water repellency", which is repelled in fields requiring a clean glass surface, is manifested by a very small amount of organic substances adsorbed on the surface.

【0004】したがってガラス基板周辺の雰囲気の清浄
化、ガラス基板表面に接触または近傍に存在する材料の
選択により極微量有機物の吸着を完全に回避することは
きわめて困難であった。
Therefore, it has been extremely difficult to completely avoid the adsorption of trace amounts of organic substances by cleaning the atmosphere around the glass substrate and selecting a material in contact with or near the glass substrate surface.

【0005】またガラス基板が建築用、車両用の板ガラ
ス、テレビブラウン管ガラス等のような大型かつ多量に
取り扱われるものにあっては高度な雰囲気調整、関連材
料の選択はコスト上むずかしく、合紙、スペーサー、段
ボール紙等の不十分な材料の使用によらざるを得ず、表
面汚染の回避は、より困難であった。
When the glass substrate is handled in large and large quantities, such as architectural and vehicular plate glass, television cathode ray tube glass, etc., it is difficult to adjust the atmosphere and select related materials at a high cost. The use of insufficient materials such as spacers, corrugated cardboard, etc. has had to be used, and avoiding surface contamination has been more difficult.

【0006】また一旦付着した有機物は、ガラス表面で
あれば表面のシラノール基と水素結合を形成するなどし
て、多くの場合簡単な水洗のみでは除去されず、化学的
物理的作用を利用した洗浄を必要としコスト面での圧迫
要因となっていた。同様の状況はガラス基板に限らず清
浄な表面が要求される基体を扱う場合に共通して生ずる
問題である。
[0006] Further, once adhered organic substances are formed on the glass surface by forming hydrogen bonds with silanol groups on the surface, and are often not removed by simple water washing, but are often washed by chemical and physical actions. Was required, which was a pressure factor in cost. A similar situation is a common problem when handling not only a glass substrate but also a substrate requiring a clean surface.

【0007】本発明は、基体への汚染の付着を完全に回
避することが困難であることおよび多くの場合、基体は
保管、運搬後、各々の必要操作前に洗浄されることを勘
案し、従来に比べ簡便に付着汚染が十分に除去されうる
基体を提供する。
The present invention takes into account that it is difficult to completely avoid contamination of the substrate and that the substrate is often washed after storage, transport and before each required operation, Provided is a substrate capable of easily removing adhesion contamination more easily than before.

【0008】[0008]

【課題を解決するための手段】本発明は、表面に水溶性
塩が塗布され、水に溶解、脱離する水溶性塩被膜が形成
された基体であって、該水溶性塩が、炭酸塩、炭酸水素
塩、硝酸塩、リン酸塩、ケイ酸塩、ホウ酸塩およびこれ
らの複塩からなる群から選ばれた1種以上である、水溶
性塩が塗布された基体を提供する。
SUMMARY OF THE INVENTION The present invention relates to a substrate having a water-soluble salt coated on its surface and having a water-soluble salt film that dissolves and desorbs in water, wherein the water-soluble salt is a carbonate. , bicarbonate, nitrate, phosphate, silicate, at least one member selected from the borates and the group consisting of double salts, that provides a substrate water-soluble salts is applied.

【0009】発明における水溶性塩としては、炭酸
塩、炭酸水素塩、硝酸塩、リン酸塩、ケイ酸塩、ホウ酸
塩およびこれらの複塩からなる群から選ばれた1種以上
である水溶性塩が用いられる。特に、リチウム、ナトリ
ウム、カリウム等の炭酸塩、硝酸塩、リン酸塩、ケイ酸
塩、ホウ酸塩などの水溶性塩が好ましく用いられる
発明においては、また、ゼオライト、ベントナイト、含
水ケイ酸アルミニウム等の、水に微小粒子として分散す
るコロイド性物質も使用できる。
The water-soluble salt in the present invention is at least one water-soluble salt selected from the group consisting of carbonates, bicarbonates, nitrates, phosphates, silicates, borates and double salts thereof. Sex salts are used. In particular, water-soluble salts such as carbonates such as lithium, sodium and potassium, nitrates, phosphates, silicates and borates are preferably used . In the present invention, a colloidal substance dispersed as fine particles in water, such as zeolite, bentonite, and hydrous aluminum silicate, can also be used.

【0010】発明における基体としては、ガラス、プ
ラスチックス、セラミックス、単結晶体、およびこれら
の表面に無機物または有機物がコーティングされたもの
からなる群から選ばれる基体が好ましい
[0010] The substrate in the present invention is preferably a substrate selected from the group consisting of glass, plastics, ceramics, single crystal, and those whose surfaces are coated with an inorganic or organic substance .

【0011】基体がガラスの場合には、ガラス表面を若
干量溶解するとの理由から、水溶性塩はアルカリ性塩で
あることが好ましい。アルカリ性塩としては、トリポリ
リン酸ナトリウム、セスキ炭酸ナトリウム、炭酸水素ナ
トリウム、炭酸ナトリウム、四ホウ酸ナトリウムおよび
四ホウ酸カリウムからなる群から選ばれた1種以上が挙
げられる。
When the substrate is glass, the water-soluble salt is preferably an alkaline salt, because the glass surface is slightly dissolved. Examples of the alkaline salt include one or more selected from the group consisting of sodium tripolyphosphate, sodium sesquicarbonate, sodium hydrogen carbonate, sodium carbonate, sodium tetraborate, and potassium tetraborate.

【0012】また、基体の検査等、透明性が要求される
場合には四ホウ酸カリウムのように風解等の変化により
白濁しない物質を用いることが望ましい。
When transparency is required, for example, for inspection of a substrate, it is desirable to use a substance such as potassium tetraborate that does not become cloudy due to a change in efflorescence or the like.

【0013】水溶性塩の塗布方法は水溶液としてスプレ
イ、ディップ、またはロール状の布やスポンジにしみ込
ませて表面に付与する等の方法がとりうる。水溶性塩の
水溶液濃度は0.01mol/l前後が水洗時の除去の
容易さ、コスト、廃液処理の面で望ましいが、基体の種
類、用途、汚染の状態により最適値が異なる。
The method of applying the water-soluble salt may be, for example, a method of impregnating a spray, dip, or roll-shaped cloth or sponge as an aqueous solution and applying it to the surface. The aqueous solution concentration of the water-soluble salt is preferably about 0.01 mol / l from the viewpoint of ease of removal at the time of washing, cost, and waste liquid treatment, but the optimum value varies depending on the type of the substrate, the application, and the state of contamination.

【0014】また、工程上の制約から乾燥時間を短くす
る必要がある場合には1〜10容量%のエチルアルコー
ル等の有機溶媒を加え強制的に風乾することにより、乾
燥時間を10分の1以下に短縮できる。
If it is necessary to shorten the drying time due to process restrictions, the drying time is reduced to 1/10 by adding 1 to 10% by volume of an organic solvent such as ethyl alcohol and forcibly air-drying. It can be shortened to the following.

【0015】基体を清浄化する場合は、洗浄剤として、
水および/または界面活性剤からなる洗浄剤を用い、洗
浄用水槽への浸漬、洗浄用水の散布で十分な効果があ
る。さらに超音波装置やブラシの併用によっても効果の
向上が期待される。
When cleaning the substrate, as a cleaning agent,
Using a cleaning agent composed of water and / or a surfactant, immersion in a cleaning water tank and spraying of the cleaning water have a sufficient effect. Furthermore, the effect can be expected to be improved by using an ultrasonic device or a brush in combination.

【0016】[0016]

【作用】本発明において、水溶性塩が塗布された基体表
面に飛来した汚染物質は水溶性塩被膜上に付着すること
となり、基体の表面には直接接触しない。この状態の基
体を水洗した場合、汚染物質は、水に溶解、脱離する水
溶性塩被膜に同伴され容易に基体から除去され、清浄な
基体表面が得られる。
In the present invention, the contaminants flying on the surface of the substrate coated with the water-soluble salt adhere to the water-soluble salt film and do not directly contact the surface of the substrate. When the substrate in this state is washed with water, contaminants are easily removed from the substrate by being accompanied by the water-soluble salt film which dissolves and desorbs in water, and a clean substrate surface is obtained.

【0017】また、水溶性塩被膜自体に電気伝導性があ
るため帯電防止効果によりゴミが付着しにくい。特にテ
レビパネル表面に付着し、後工程の熱処理により焼き付
き、欠点となる紙粉と呼ばれるゴミ低減にも効果があ
る。
Further, since the water-soluble salt film itself has electric conductivity, dust is hardly attached due to an antistatic effect. In particular, it adheres to the surface of a television panel, burns in by a heat treatment in a later step, and is effective in reducing dust, which is a defect, called paper powder.

【0018】[0018]

【実施例】実施例1 表1にソーダ石灰ガラスへの実施例を示す。ソーダ石灰
ガラスは1.1mm厚のフロートガラスである。このガ
ラスのトップ面(スズ浴中のスズ非接触面)をセリアに
て研磨、水洗、乾燥、水溶性塩の塗布、汚染操作などの
各種処理を実施した場合について、このガラスのトップ
面の接触角を測定し清浄度を評価した。
EXAMPLES Example 1 Table 1 shows an example for soda-lime glass. Soda lime glass is a 1.1 mm thick float glass. When the glass top surface (the tin non-contact surface in the tin bath) is subjected to various treatments such as polishing, washing, drying, application of a water-soluble salt, and contamination operation with ceria, contact of the glass top surface is performed. The corners were measured and the cleanliness was evaluated.

【0019】なお、汚染を付着させるための操作「汚染
操作」は、代表的可塑剤でありガラスの撥水性原因とな
りやすいジオクチルフタレート(DOP)を底部に満た
したデシケーター中にガラス試験片を中空に吊して48
時間密封した。
The operation for adhering contamination, "contamination operation", is performed by hollowing a glass test piece in a desiccator filled with dioctyl phthalate (DOP), which is a typical plasticizer and tends to cause water repellency of glass. Hanging 48
Sealed for hours.

【0020】また、この場合の水溶性塩の塗布は、トリ
ポリリン酸ナトリウム、セスキ炭酸ナトリウム、四ホウ
酸ナトリウム、四ホウ酸カリウムの各0.01mol/
l水溶液にガラスを浸漬し乾燥した。水洗は室温の純水
の流水下で30秒間行った。
In this case, the water-soluble salt is applied at a rate of 0.01 mol / each of sodium tripolyphosphate, sodium sesquicarbonate, sodium tetraborate and potassium tetraborate.
The glass was immersed in an aqueous solution and dried. The water washing was performed for 30 seconds under flowing pure water at room temperature.

【0021】表1に示す通り、直接汚染操作を行ったガ
ラスBは水洗後(ガラスC)も接触角が低下せずDOP
による汚染が除去されないのに対し、トリポリリン酸ナ
トリウム、セスキ炭酸ナトリウム、四ホウ酸ナトリウ
ム、四ホウ酸カリウムを塗布したガラスD、ガラスF、
ガラスH、ガラスJでは水洗後の接触角は汚染操作前の
レベル(ガラスA)まで低下しDOPの汚染が水洗によ
り容易に除去され、清浄面が回復したことがわかる。
As shown in Table 1, the glass B that had been subjected to the direct contamination operation did not show a decrease in the contact angle even after washing with water (glass C).
Glass D coated with sodium tripolyphosphate, sodium sesquicarbonate, sodium tetraborate, potassium tetraborate, glass F,
It can be seen that the contact angles of the glass H and the glass J after the water washing were reduced to the level (glass A) before the contamination operation, the DOP contamination was easily removed by the water washing, and the clean surface was recovered.

【0022】本例によりクリーンルーム等に保管された
ガラスに有機物分子が飛来、吸着することによる汚染が
きわめて簡便な水洗で除去しうることがわかる。
According to this example, it can be understood that the contamination caused by the organic molecules flying and adsorbing on the glass stored in a clean room or the like can be removed by a very simple washing with water.

【0023】実施例2 表2にテレビファンネル用ガラスに実施した例を示す。
テレビファンネル用ガラスを約1cm角に切断し、1%
HF−1%H2 SO4 の水溶液に3分間浸漬、水洗、乾
燥、水溶性塩の塗布、汚染操作などの各種処理を実施し
た場合について、ガラス表面の汚染の除去状況をESC
A(光電子分光法)のピーク強度比(C1s/Si2p)に
より測定した。ただし、C1sピークは284.6eVの
ピークを測定、Si2pピークは103.4eVのピーク
を測定した。
Example 2 Table 2 shows an example in which the invention was applied to glass for a TV funnel.
Cut the glass for TV funnel into 1cm square, 1%
ESC shows the removal status of contamination on the glass surface when various treatments such as immersion in HF-1% H 2 SO 4 aqueous solution for 3 minutes, washing with water, drying, application of a water-soluble salt, and contamination operation were performed.
It was measured by the peak intensity ratio of A (photoelectron spectroscopy) (C 1s / Si 2p ). However, the C 1s peak measured a peak of 284.6 eV, and the Si 2p peak measured a peak of 103.4 eV.

【0024】なお、水溶性塩の塗布は、トリポリリン酸
ナトリウム、炭酸水素ナトリウム、四ホウ酸ナトリウ
ム、四ホウ酸カリウムの各0.01mol/l水溶液に
ガラスを浸漬し乾燥した。汚染操作、水洗は、実施例1
と同様である。
The water-soluble salt was applied by dipping the glass in a 0.01 mol / l aqueous solution of sodium tripolyphosphate, sodium hydrogen carbonate, sodium tetraborate, and potassium tetraborate, and drying. Pollution operation and water washing were performed in Example 1.
Is the same as

【0025】表2に示す通り「汚染操作」後DOPの付
着を示すESCAピーク強度比がいずれのガラスにおい
ても増加するが、水溶性塩を塗布していないガラスNで
は値の低下がほとんど見られないのに対し、トリポリリ
ン酸ナトリウム、炭酸水素ナトリウム、四ホウ酸ナトリ
ウム、四ホウ酸カリウムを塗布したガラスP、ガラス
R、ガラスT、ガラスVでは初期の値にまで低下し、D
OPが水洗により除去されたことがわかる。
As shown in Table 2, the ESCA peak intensity ratio indicating the attachment of DOP after the "contamination operation" was increased in any of the glasses, but the value was almost decreased in the glass N not coated with the water-soluble salt. In contrast, in glass P, glass R, glass T, and glass V coated with sodium tripolyphosphate, sodium hydrogen carbonate, sodium tetraborate, and potassium tetraborate, the values decreased to the initial values, and D
It can be seen that OP was removed by washing with water.

【0026】本例により保管中にファンネル内面が撥水
化し、水洗によっても回復せず、カーボンスラリー(ダ
グ)のはじき不良を起こすという工程上の問題を解決し
うることが示される。
This example shows that the inner surface of the funnel becomes water-repellent during storage and is not recovered even by washing with water, which can solve the problem in the process of causing repelling failure of the carbon slurry (dug).

【0027】実施例3 光音響素子の媒体である石英ガラスと圧電体結晶である
ニオブ酸リチウム(LiNbO3 )に実施した例を示
す。工程中に受け入れた石英ガラスとLiNbO3 を工
程内の洗浄ラインで洗浄を行った。洗浄した試料につい
て、トリポリリン酸ナトリウム0.01mol/l水溶
液に浸漬乾燥した場合と、浸漬しない場合のそれぞれの
場合についてクリーンルーム内に4日間保管し水洗し
た。各処理後の試料の表面の接触角を測定した結果を表
3に示す。
Example 3 An example in which the present invention is applied to quartz glass as a medium of a photoacoustic element and lithium niobate (LiNbO 3 ) as a piezoelectric crystal will be described. The quartz glass and LiNbO 3 received during the process were cleaned in a cleaning line in the process. The washed sample was immersed and dried in a 0.01 mol / l aqueous solution of sodium tripolyphosphate, and was stored in a clean room for 4 days and washed with water in both cases of immersion and non-immersion. Table 3 shows the results of measuring the contact angle of the surface of the sample after each treatment.

【0028】表3より保管中に光音響素子媒体および圧
電体結晶表面に付着した汚染がトリポリリン酸ナトリウ
ムの塗布により簡便な水洗で除去できることがわかる。
Table 3 shows that the contamination attached to the surface of the photoacoustic element medium and the surface of the piezoelectric crystal during storage can be removed by simple washing with water by applying sodium tripolyphosphate.

【0029】実施例4 人工衛星用太陽電池カバーガラスに実施した例を示す。
カバーガラスをイソプロピルアルコールにて洗浄した
後、トリポリリン酸ナトリウム0.01mol/l水溶
液、セスキ炭酸ナトリウム0.01mol/l水溶液ま
たは四ホウ酸ナトリウム0.01mol/l水溶液に浸
漬し乾燥後、発泡ポリスチレン容器に10日保管し水洗
した後の接触角を測定した結果を表4に示す。また、各
々の水溶液に浸漬しない場合の水洗前後の接触角をブラ
ンクとして表4に示す。
Example 4 An example in which the invention is applied to a solar cell cover glass for an artificial satellite will be described.
After the cover glass is washed with isopropyl alcohol, it is immersed in a 0.01 mol / l aqueous solution of sodium tripolyphosphate, a 0.01 mol / l aqueous solution of sodium sesquicarbonate or a 0.01 mol / l aqueous solution of sodium tetraborate, dried, and then dried. Table 4 shows the results of measuring the contact angles after storage for 10 days and washing with water. In addition, Table 4 shows the contact angles before and after water washing when not immersed in each aqueous solution as blanks.

【0030】表4より保管中に発泡ポリスチレン容器か
ら転移した汚染が、トリポリリン酸ナトリウム、セスキ
炭酸ナトリウムまたは四ホウ酸ナトリウムを表面に塗布
しておくことにより、水洗で容易に除去されることがわ
かる。
Table 4 shows that contamination transferred from the expanded polystyrene container during storage can be easily removed by washing with water by applying sodium tripolyphosphate, sodium sesquicarbonate or sodium tetraborate on the surface. .

【0031】実施例5 液晶用超薄板ガラス(1.1mm厚)に実施した例を示
す。超薄板ガラスを洗浄後、トリポリリン酸ナトリウム
および四ホウ酸ナトリウムの各々の0.01mol/l
水溶液または0.1mol/l水溶液に浸漬し、自然乾
燥した後、ガラス用の合紙をガラス間に挿入した。これ
を20℃、湿度80%RHの恒温恒湿槽に10日間保管
した後に水洗した。水洗前後の接触角(°)を測定した
結果を表5に示す。また、トリポリリン酸ナトリウム水
溶液に浸漬せず同様の操作を行った場合(ブランク)を
併せて表5に示す。
Example 5 An example in which the invention is applied to an ultra-thin glass sheet for liquid crystal (1.1 mm thick) will be described. After washing the ultra-thin glass, 0.01 mol / l of each of sodium tripolyphosphate and sodium tetraborate
After being immersed in an aqueous solution or a 0.1 mol / l aqueous solution and air-dried, an interleaf paper for glass was inserted between the glasses. This was stored in a thermo-hygrostat at 20 ° C. and 80% RH for 10 days, and then washed with water. Table 5 shows the results of measuring the contact angle (°) before and after washing. Table 5 also shows a case where the same operation was performed without immersion in an aqueous solution of sodium tripolyphosphate (blank).

【0032】表5より保管中にガラス用合紙からガラス
の表面に転移した汚染(紙アト)が、合紙の種類、性状
(油脂分、吸水性、表面平滑度等)にかかわらず、水洗
により容易に除去されることがわかる。
From Table 5, the contamination (paper at) transferred from the glass insert to the glass surface during storage was washed with water regardless of the type and properties of the insert (oil, fat, water absorption, surface smoothness, etc.). It can be seen that it is easily removed.

【0033】[0033]

【表1】 [Table 1]

【0034】[0034]

【表2】 [Table 2]

【0035】[0035]

【表3】 [Table 3]

【0036】[0036]

【表4】 [Table 4]

【0037】[0037]

【表5】 [Table 5]

【0038】[0038]

【発明の効果】本発明の基体を水洗することによって、
基体表面の汚染物質は、水に溶解、脱離する水溶性塩被
膜に同伴され容易に基体から除去され、清浄な基体表面
が得られる。したがって、基体を製造、保管、運搬する
雰囲気の清浄度を、基体表面に付着する汚染物質を低減
する目的で高度に高める必要がないという効果が得られ
る。また、帯電防止効果によりチリ等が付着しにくいと
の効果もある。
By washing the substrate of the present invention with water,
Contaminants on the substrate surface are easily removed from the substrate by being accompanied by a water-soluble salt film which dissolves and desorbs in water, and a clean substrate surface is obtained. Therefore, an effect is obtained that the cleanliness of the atmosphere in which the substrate is manufactured, stored, and transported does not need to be highly enhanced for the purpose of reducing contaminants adhering to the substrate surface. In addition, there is also an effect that dust and the like hardly adhere due to an antistatic effect.

【0039】また、基体を製造、保管、運搬する際に、
その基体表面に接触する合紙、スペーサーなどの材料
や、近傍に存在する段ボール、発泡スチロールなどの材
料からの汚染物質の転移を低減するために、従来制約さ
れていたこれら材料の選択許容範囲が大きく拡大すると
いう効果が得られる。
When manufacturing, storing, and transporting the substrate,
In order to reduce the transfer of contaminants from materials such as interleaf paper and spacers that come into contact with the substrate surface and materials such as corrugated cardboard and styrofoam that exist in the vicinity, the selection tolerance of these materials, which was conventionally restricted, is large. The effect of enlargement is obtained.

【0040】さらに、使用前に実施する水洗工程が簡便
となるという効果が得られる。即ち、洗剤として用いる
界面活性剤、洗浄槽に具備する超音波洗浄器、ブラシ等
が省略されても同等以上の汚染除去効果が期待できる。
Further, there is obtained an effect that the washing step performed before use is simplified. That is, even if a surfactant used as a detergent, an ultrasonic cleaner provided in a cleaning tank, a brush, and the like are omitted, the same or better contamination removing effect can be expected.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 平6−116512(JP,A) 特開 平6−51523(JP,A) 特開 昭56−25970(JP,A) 特開 昭59−96280(JP,A) (58)調査した分野(Int.Cl.7,DB名) C09K 3/00 112 B08B 7/00 B08B 17/00 C03C 23/00 ────────────────────────────────────────────────── ─── Continuation of front page (56) References JP-A-6-116512 (JP, A) JP-A-6-51523 (JP, A) JP-A-56-25970 (JP, A) JP-A-59-1979 96280 (JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) C09K 3/00 112 B08B 7/00 B08B 17/00 C03C 23/00

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】表面に水溶性塩が塗布され、水に溶解、脱
離する水溶性塩被膜が形成された基体であって、該水溶
性塩が、炭酸塩、炭酸水素塩、硝酸塩、リン酸塩、ケイ
酸塩、ホウ酸塩およびこれらの複塩からなる群から選ば
れた1種以上である、水溶性塩が塗布された基体。
1. A substrate having a surface coated with a water-soluble salt to form a water-soluble salt film which dissolves and desorbs in water, wherein the water-soluble salt is carbonate, bicarbonate, nitrate, phosphorus A substrate coated with a water-soluble salt, which is at least one selected from the group consisting of acid salts, silicates, borates and double salts thereof.
【請求項2】水溶性塩が、トリポリリン酸ナトリウム、
セスキ炭酸ナトリウム、炭酸水素ナトリウム、炭酸ナト
リウム、四ホウ酸ナトリウムおよび四ホウ酸カリウムか
らなる群から選ばれた1種以上であり、かつ、基体がガ
ラスである請求項1に記載の水溶性塩が塗布された基
体。
2. The water-soluble salt is sodium tripolyphosphate,
The water-soluble salt according to claim 1, which is at least one selected from the group consisting of sodium sesquicarbonate, sodium bicarbonate, sodium carbonate, sodium tetraborate and potassium tetraborate, and wherein the substrate is glass. Coated substrate.
JP06021391A 1993-02-26 1994-02-18 Substrate coated with water-soluble salt Expired - Fee Related JP3075906B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP06021391A JP3075906B2 (en) 1993-02-26 1994-02-18 Substrate coated with water-soluble salt

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP6286293 1993-02-26
JP5-62862 1993-04-09
JP5-107778 1993-04-09
JP10777893 1993-04-09
JP06021391A JP3075906B2 (en) 1993-02-26 1994-02-18 Substrate coated with water-soluble salt

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP10928799A Division JP3659057B2 (en) 1993-02-26 1999-04-16 Cleaning method of CRT glass surface

Publications (2)

Publication Number Publication Date
JPH06340865A JPH06340865A (en) 1994-12-13
JP3075906B2 true JP3075906B2 (en) 2000-08-14

Family

ID=27283414

Family Applications (1)

Application Number Title Priority Date Filing Date
JP06021391A Expired - Fee Related JP3075906B2 (en) 1993-02-26 1994-02-18 Substrate coated with water-soluble salt

Country Status (1)

Country Link
JP (1) JP3075906B2 (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2325562B (en) * 1997-05-23 2001-08-08 Asahi Glass Co Ltd A cathode ray tube glass,a method for producing the cathode ray tube glass,and method for cleaning the cathode ray tube glass
ID21661A (en) 1997-07-16 1999-07-08 Nippon Electric Glass Co GLASS MATERIALS SURFACE COATED BY BORATE ACID AND METHODS PRODUCE THE SAME
BR9915240A (en) * 1998-11-10 2001-07-24 Nippon Sheet Glass Co Ltd Glass article, method for handling the glass article and handling tool for the glass article
US6673162B1 (en) 1999-10-08 2004-01-06 Nippon Electric Glass Co., Ltd. Glass article having surface coating of hydroxy acid and method of manufacturing the same
JPWO2007013235A1 (en) * 2005-07-29 2009-02-05 旭硝子株式会社 Glass plate with protective film
GB0525566D0 (en) * 2005-12-16 2006-01-25 Pilkington Plc Glass storage
US8316647B2 (en) * 2009-01-19 2012-11-27 General Electric Company System and method employing catalytic reactor coatings

Also Published As

Publication number Publication date
JPH06340865A (en) 1994-12-13

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