JPH03227376A - Production of inorganic electrically conductive coating material - Google Patents
Production of inorganic electrically conductive coating materialInfo
- Publication number
- JPH03227376A JPH03227376A JP2175290A JP2175290A JPH03227376A JP H03227376 A JPH03227376 A JP H03227376A JP 2175290 A JP2175290 A JP 2175290A JP 2175290 A JP2175290 A JP 2175290A JP H03227376 A JPH03227376 A JP H03227376A
- Authority
- JP
- Japan
- Prior art keywords
- antimony
- tin oxide
- solvent
- weight
- doped tin
- 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.)
- Pending
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000000463 material Substances 0.000 title abstract description 7
- 239000012799 electrically-conductive coating Substances 0.000 title 1
- 239000000843 powder Substances 0.000 claims abstract description 24
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims abstract description 21
- 229910001887 tin oxide Inorganic materials 0.000 claims abstract description 21
- 239000002904 solvent Substances 0.000 claims abstract description 15
- 239000011230 binding agent Substances 0.000 claims abstract description 13
- 239000002245 particle Substances 0.000 claims abstract description 13
- 239000002244 precipitate Substances 0.000 claims abstract description 11
- 239000004094 surface-active agent Substances 0.000 claims abstract description 9
- 238000002156 mixing Methods 0.000 claims abstract description 6
- 239000003973 paint Substances 0.000 claims description 23
- 239000003093 cationic surfactant Substances 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 23
- 239000006185 dispersion Substances 0.000 abstract description 14
- 239000000758 substrate Substances 0.000 abstract description 11
- 238000000576 coating method Methods 0.000 abstract description 10
- 239000011248 coating agent Substances 0.000 abstract description 9
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 abstract description 8
- 239000011521 glass Substances 0.000 abstract description 7
- 239000004033 plastic Substances 0.000 abstract description 5
- 229920003023 plastic Polymers 0.000 abstract description 5
- 239000007788 liquid Substances 0.000 abstract description 4
- 238000010908 decantation Methods 0.000 abstract description 3
- 238000001556 precipitation Methods 0.000 abstract description 2
- 238000000926 separation method Methods 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
- 230000000694 effects Effects 0.000 description 6
- 239000010408 film Substances 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 6
- 238000004062 sedimentation Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910052787 antimony Inorganic materials 0.000 description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 2
- FAPDDOBMIUGHIN-UHFFFAOYSA-K antimony trichloride Chemical compound Cl[Sb](Cl)Cl FAPDDOBMIUGHIN-UHFFFAOYSA-K 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000011164 primary particle Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、ガラス又はプラスチックなどの透明基材に塗
布する無機導電性塗料の製造方法に関し、さらに詳しく
は、硬化塗膜の導電性及び透明性に優れ、かつ導電性粉
末の沈降性が良好な無機導電性塗料の製造方法に関する
。Detailed Description of the Invention [Field of Industrial Application] The present invention relates to a method for producing an inorganic conductive paint to be applied to a transparent substrate such as glass or plastic. The present invention relates to a method for producing an inorganic conductive paint having excellent properties and good sedimentation properties of conductive powder.
近年、ガラス又はプラスチックなどの透明な基材に導電
性を付与することにより基材の帯電防止が図られること
が多くなっている。In recent years, it has become common to prevent static electricity on transparent substrates such as glass or plastic by imparting conductivity to them.
ガラス又はプラスチックなどの透明な基材に導電性を付
与するには、従来、基材表面にカーボン粉末、金属粉末
、カーボン繊維あるいは金属繊維を混入して導電性が付
与された塗料を塗布することが行われてきた。ところが
、この塗料では、塗膜が黒色又は灰色を呈するため、基
材の色調が損なわれてしまうという問題があった。また
、透明性を出すために、金属酸化物として酸化スズ、酸
化インジウムなどを用いても基材表面が曇るなどの問題
があり、透明性は必ずしも満足できず、また、酸化スズ
は導電性が十分でないという問題があった。また、この
塗料は放置すると、短時間に金属酸化物が沈殿してしま
うため、塗布作業上問題があった。Conventionally, to impart conductivity to a transparent substrate such as glass or plastic, the surface of the substrate is coated with a paint that is made conductive by mixing carbon powder, metal powder, carbon fiber, or metal fiber. has been carried out. However, this paint has a problem in that the paint film exhibits a black or gray color, which impairs the color tone of the base material. Furthermore, even if tin oxide, indium oxide, etc. are used as metal oxides to achieve transparency, there are problems such as clouding of the substrate surface, and transparency cannot always be satisfied.Also, tin oxide has poor conductivity. The problem was that it wasn't enough. Furthermore, if this paint is left to stand, metal oxides will precipitate in a short period of time, which poses a problem in the application process.
このような塗膜の透明性導電性及び沈降性に関する問題
点を解決するため、例えば、特公昭61−9343号公
報には、アンチモンがドープされた酸化スズからなる導
電性粉末を用いた導電性塗料が開示されている。しかし
ながら、この導電性塗料では、特定量の塩化スズと塩化
アンチモンとを溶解させた水溶液を、加熱水中に注いで
前記塩化物を加水分解させ、析出する沈殿物をう戸別洗
浄した後、加熱処理することによって、0.2μm以下
の導電性粉末を製造するため、以下のような問題点が生
じてきた。すなわち、上記公報に開示されているように
ハロゲン化物を加水分解することによって液中に導電性
微粉末の前駆体を沈殿させると、得られる沈殿物は極め
て微細な一次粒子が凝集した状態にある。このため、こ
の沈殿物を;戸別洗浄した後、加熱処理して更に粉砕し
ても一次粒子が凝集した二次凝集粒子も含有され、これ
をバインダー樹脂に分散させても、すくに沈降し、また
、これを塗布した塗膜は透明性に劣るとG・ら問題があ
った。In order to solve such problems regarding the transparency, conductivity and sedimentation of coating films, for example, Japanese Patent Publication No. 61-9343 discloses a conductive powder using conductive powder made of tin oxide doped with antimony. Paint is disclosed. However, in this conductive paint, an aqueous solution in which specific amounts of tin chloride and antimony chloride are dissolved is poured into heated water to hydrolyze the chloride, and the precipitate is washed separately, followed by heat treatment. In order to produce conductive powder with a diameter of 0.2 μm or less, the following problems have arisen. That is, when a conductive fine powder precursor is precipitated in a liquid by hydrolyzing a halide as disclosed in the above publication, the resulting precipitate is in a state where extremely fine primary particles aggregate. . For this reason, even if this precipitate is washed door-to-door, then heat-treated and further crushed, it still contains secondary agglomerated particles, which are agglomerated primary particles, and even if these are dispersed in a binder resin, they easily settle out Furthermore, there was a problem with G. et al. that the coating film coated with this coating had poor transparency.
これに加えて、たとえ強力な粉砕によって更に微粉化し
ても、粒子は本来凝集力が強いためにすぐに再凝集して
しまい、上記と同様な問題が生した。In addition to this, even if the particles were further pulverized by powerful pulverization, the particles would quickly re-agglomerate due to their inherently strong cohesive force, resulting in the same problem as above.
[発明が解決しようとする課題]
本発明は、上記のような従来技術に伴う問題点を解決す
るものであって、アンチモンがドープされた酸化スズ粉
末を無機塗料中に分散させても沈降性が良好で、かつ硬
化塗膜の導電性及び透明性に優れ、また、硬化温度も1
00°C以上の温度を任意に選択することができ、基材
に対する悪影響を与えない無機導電性塗料の製造方法を
提供することを目的とする。[Problems to be Solved by the Invention] The present invention solves the problems associated with the prior art as described above, and it is possible to solve the problems associated with the prior art as described above. The cured coating film has good conductivity and transparency, and the curing temperature is 1.
It is an object of the present invention to provide a method for producing an inorganic conductive paint that can arbitrarily select a temperature of 00°C or higher and does not have a negative effect on the base material.
本発明は、(A)アンチモンがドープされた粒径0.2
μm以下の酸化スズ粉末1〜10重量%、溶剤99〜9
0重量%及びアンチモンがトープされた酸化スズ粉末の
重量の1〜10重量%の界面活性剤を分散機で分散させ
て、沈殿物を除去した後、(B)無機バインダー及び(
C)溶剤を添加混合することを特徴とする無機導電性塗
料の製造方法に関する。The present invention is characterized in that (A) antimony-doped particles with a diameter of 0.2
1-10% by weight of tin oxide powder less than μm, solvent 99-9
After removing the precipitate by dispersing a surfactant in an amount of 0% by weight and 1 to 10% by weight based on the weight of the antimony-topped tin oxide powder, (B) an inorganic binder and (
C) A method for producing an inorganic conductive paint characterized by adding and mixing a solvent.
次に、本発明に使用する材料について述べる。Next, materials used in the present invention will be described.
まず、(A)成分について述べると、使用するアンチモ
ンのドープされた酸化スズ(以下、アンチモンドープ酸
化スズと記す)粉末は、例えば塩酸の水溶液、アルコー
ル溶液又はこれらの混合溶液に塩化スズと塩化アンチモ
ンとを溶解させて得られる溶液を、加熱水中に加えて沈
殿物を析出させ、これを;戸別洗浄した後、焼成、粉砕
することによって製造できる。この粉末の粒径は0.2
μm以下であることを必要とし、好ましくは0.05μ
m以下である。粒径が0.2μmを越えると、粒子が粗
くなり、薄膜形成ができず、透明性が悪くなり、かつ沈
降が起こり易い。アンチモンドープ酸化スズの好適な例
としては、三菱金属■製のT1などがある。First, regarding component (A), the antimony-doped tin oxide (hereinafter referred to as antimony-doped tin oxide) powder used is, for example, a solution of tin chloride and antimony chloride in an aqueous solution of hydrochloric acid, an alcohol solution, or a mixed solution thereof. It can be produced by adding a solution obtained by dissolving these into heated water to precipitate a precipitate, which is then washed door to door, then calcined and pulverized. The particle size of this powder is 0.2
Must be less than μm, preferably 0.05 μm
m or less. When the particle size exceeds 0.2 μm, the particles become coarse, cannot form a thin film, have poor transparency, and tend to cause sedimentation. A suitable example of antimony-doped tin oxide is T1 manufactured by Mitsubishi Metals.
溶剤としては、メタノール、エタノール、イソプロピル
アルコール、ブタノール、オクチルアルコール、ジアセ
トンアルコール等のアルコール類、アセトン、メチルエ
チルケトン、メチルイソブチルケトン等のケトン類、エ
チレングリコールモノメチルエーテル、エチレングリコ
ールモノエチルエーテル等のエーテル類、酢酸エチル、
酢酸ブチル等のエステル類などの溶剤が単独で又は混合
して使用される。Examples of solvents include alcohols such as methanol, ethanol, isopropyl alcohol, butanol, octyl alcohol, and diacetone alcohol, ketones such as acetone, methyl ethyl ketone, and methyl isobutyl ketone, and ethers such as ethylene glycol monomethyl ether and ethylene glycol monoethyl ether. ,Ethyl acetate,
Solvents such as esters such as butyl acetate are used alone or in combination.
界面活性剤としては、カチオン系、アニオン系あるいは
ノニオン系の各種界面活性剤が使用可能であるが、分散
性の点からカチオン系界面活性剤を使用することが特に
好ましい。界面活性剤の好適な例として、ビックケミ−
ジャパン■製のアンチ−テラービイ(Anti−Ter
ra−P) 、デイスパービック(Disperbyk
) 130 (いずれも商品名)などがある。As the surfactant, various cationic, anionic, or nonionic surfactants can be used, but it is particularly preferable to use a cationic surfactant from the viewpoint of dispersibility. As a suitable example of surfactant, Bicchem
Anti-Terby made in Japan
ra-P), Disperbyk
) 130 (all product names).
配合について述べると、アンチモンドープ酸化スズ粉末
は、1〜10重量%の量で使用され、溶剤は99〜90
重量%の量で使用される。1重量%未満では濃度が低く
なりすぎ、後述する無機導電性塗料の濃度も低くなりす
ぎて実用上問題がある。また、10重量%を越えると粘
度が上がるため分散性が悪くなる。Regarding the formulation, the antimony-doped tin oxide powder is used in an amount of 1-10% by weight, and the solvent is used in an amount of 99-90% by weight.
Used in amounts of % by weight. If it is less than 1% by weight, the concentration will be too low, and the concentration of the inorganic conductive paint described below will also be too low, causing a practical problem. Moreover, if it exceeds 10% by weight, the viscosity increases and the dispersibility deteriorates.
界面活性剤の添加量は、アンチモンドープ酸化スズ粉末
の重量の1〜10重量%とする。1重量%未満では、界
面活性剤の効果が発現せず、分散性が劣る。10重量%
を越えると、透過性及び導電性が悪くなり、また、界面
活性剤によっては分散効果よりも逆に凝集効果を呈し、
沈降性が悪くなる。The amount of surfactant added is 1 to 10% by weight of the antimony-doped tin oxide powder. If the amount is less than 1% by weight, the effect of the surfactant will not be expressed and the dispersibility will be poor. 10% by weight
If it exceeds this, permeability and conductivity will deteriorate, and some surfactants may exhibit an aggregation effect rather than a dispersion effect.
Sedimentability deteriorates.
また、分散機としては、ホモミキサー、ホモジナイザー
、アトライター、ボールミル、サンドミル、ロール、超
音波などが使用される。これらのうち、分散性の点から
ホモミキサー、ホモジナイザー、ボールミル及びサンド
ミルが好ましい。Further, as a dispersing machine, a homomixer, a homogenizer, an attritor, a ball mill, a sand mill, a roll, an ultrasonic wave, etc. are used. Among these, homomixers, homogenizers, ball mills, and sand mills are preferred from the viewpoint of dispersibility.
分散機で処理した後、遠心分離を行うか、数時間〜数日
静置すると、上層のアンチモンドープ酸化スズの分散液
と下層の沈殿物とに分かれるので、デカンテーションな
どの方法で下層の沈殿物を取り除く。このように処理し
た分散液の粒子を電子顕微鏡で観察すると、処理前に比
べて二次凝集粒子がかなり減少していることが確認され
た。After processing with a dispersion machine, if centrifugation is performed or left to stand for several hours to several days, it will separate into an upper layer of antimony-doped tin oxide dispersion and a lower layer of precipitate. remove things. When the particles of the dispersion treated in this manner were observed under an electron microscope, it was confirmed that the number of secondary agglomerated particles was considerably reduced compared to before treatment.
次に、(B)成分の無機バインダーとしては、シリカ系
の無機バインダーがあり、例えばテトラエトキシシラン
、テトラメトキシシランなどが使用でき、また、これら
をアルコール、ケトンなどに溶解し、水及び酸を加え、
反応させて得られるポリマー、市販のシリカ系ポリマー
などが使用できる。この例として、多摩化学工業■製の
エチルシリケート28、エチルシリケート40(いずれ
も商品名)などがある。Next, as the inorganic binder of component (B), there are silica-based inorganic binders, such as tetraethoxysilane and tetramethoxysilane, which can be used.Also, these can be dissolved in alcohol, ketone, etc., and water and acid are dissolved. In addition,
Polymers obtained by reaction, commercially available silica-based polymers, etc. can be used. Examples of this include ethyl silicate 28 and ethyl silicate 40 (both trade names) manufactured by Tama Chemical Industry (2).
(C)成分の溶剤とは、(B)成分の無機バインダーを
溶解できるものであれば、各種のものを使用でき、(A
)成分に使用した溶剤が使用可能である。また、無機バ
インダーの硬化性を良くするために水、硝酸、塩酸、硫
酸などの酸を添加することも可能である。The solvent of component (C) can be any of various solvents as long as it can dissolve the inorganic binder of component (B).
) The solvent used for the component can be used. Furthermore, in order to improve the curability of the inorganic binder, it is also possible to add water, and acids such as nitric acid, hydrochloric acid, and sulfuric acid.
次に、(A)成分中のアンチモンドープ酸化スズ粉末、
(B)及び(C)成分の配合比について述べる。塗膜の
透過性と導電性からアンチモンドープ酸化スズ粉末/無
機バインダーの重量比は1/9〜6/4の範囲が好まし
い。6/4を越えると透過性が劣り、1/9より小さい
と導電性が劣る。Next, antimony-doped tin oxide powder in component (A),
The blending ratio of components (B) and (C) will be described. In view of the permeability and conductivity of the coating film, the weight ratio of antimony-doped tin oxide powder/inorganic binder is preferably in the range of 1/9 to 6/4. If it exceeds 6/4, the transmittance will be poor, and if it is less than 1/9, the conductivity will be poor.
また、溶剤量は、アンチモンドープ酸化スズ粉末と無機
バインダーとの合計10重量部に対して200〜500
0重量部が好ましい。The amount of solvent is 200 to 500 parts by weight per 10 parts by weight of the antimony-doped tin oxide powder and the inorganic binder.
0 parts by weight is preferred.
本発明の方法で得られる無機導電性塗料は、スピンコー
ティング、デイツプコーティング、スプレーコーティン
グ等の一般的なコーティング法で塗布することができ、
室温から100″C程度で溶剤を乾燥した後、100″
C以上での温度で硬化させることができるが、基材の割
れ、溶解などを考慮すると、硬化温度は130〜200
°Cが好ましい。The inorganic conductive paint obtained by the method of the present invention can be applied by general coating methods such as spin coating, dip coating, and spray coating.
After drying the solvent at about 100"C from room temperature,
It can be cured at a temperature of 130 to 200 C or higher, but considering cracks and melting of the base material, the curing temperature should be 130 to 200 C.
°C is preferred.
[実施例]
次に、実施例により本発明をさらに詳しく説明する。な
お、実施例及び比較例中「部」及び「%」は、特に断ら
ない限り、それぞれ「重量部」及び「重量%」を意味す
る。[Example] Next, the present invention will be explained in more detail with reference to Examples. In the Examples and Comparative Examples, "parts" and "%" mean "parts by weight" and "% by weight," respectively, unless otherwise specified.
実施例I
T−1(三菱金属■製アンチモンドープ酸化スズ粉末の
商品名、アンチモンドープ量10%、成粒子の粒径0.
05μm)50部、エタノール950部及びアンチ−テ
ラービイ(Anti−丁erra−P)(ビ・7クケミ
一ジヤバン■製カチオン系界面活性剤の商品名)3.5
部をホモミキサーで5時間分散させた。これを24時間
静置した後、デカンテーションにより沈殿物を除去し、
分散液Aを得た。Example I T-1 (trade name of antimony-doped tin oxide powder manufactured by Mitsubishi Metals ■, antimony doping amount 10%, particle size of formed particles 0.
05 μm) 50 parts, 950 parts of ethanol, and Anti-Terra-P (trade name of a cationic surfactant manufactured by Bi-7 Kemi-Jiyaban) 3.5
The mixture was dispersed in a homomixer for 5 hours. After leaving this for 24 hours, the precipitate was removed by decantation,
Dispersion A was obtained.
この分散液Aのアンチモンドープ酸化スズ粉末の濃度を
測定すると、3.0%であった。この分散液A100部
、エチルシリケート40(多摩化学工業■製のシリカ系
無機バインダーの商品名、有効シリカ量40%)7.5
部及びエタノール200部を10時間混合撹拌して無機
導電性塗料を得た。When the concentration of the antimony-doped tin oxide powder in this dispersion A was measured, it was 3.0%. 100 parts of this dispersion A, ethyl silicate 40 (trade name of silica-based inorganic binder manufactured by Tama Chemical Industry ■, effective silica amount 40%) 7.5
1 part and 200 parts of ethanol were mixed and stirred for 10 hours to obtain an inorganic conductive paint.
実施例2
実施例1で得た分散液A100部、エチルシリケート2
8(多摩化学工業株製のシリカ系無機バインダーの商品
名、有効シリカ量28%)25部、エタノール200部
及び硝酸0.2部を10時間混合撹拌して無機導電性塗
料を得た。Example 2 100 parts of dispersion A obtained in Example 1, 2 ethyl silicate
8 (trade name of a silica-based inorganic binder manufactured by Tama Chemical Industry Co., Ltd., effective silica content 28%), 25 parts of ethanol, 200 parts of ethanol, and 0.2 part of nitric acid were mixed and stirred for 10 hours to obtain an inorganic conductive paint.
実施例3
実施例1で使用したT−1,50部、エタノール950
部及び実施例1で使用したアンチーテラビイ2.5部を
ホモミキサーで10時間分散させた。これを24時間静
置した後、デカンテーションにより沈殿物を除去し、分
散液Bを得た。この分散液Bの酸化スズ粉末の濃度を測
定すると、2.8%であった。この分散液B200部、
エチルシリケート40を10部及びエタノール280部
を10時間混合撹拌して無機導電性塗料を得た。Example 3 50 parts of T-1 used in Example 1, 950 ethanol
1 part and 2.5 parts of Antitelabi used in Example 1 were dispersed in a homomixer for 10 hours. After allowing this to stand for 24 hours, the precipitate was removed by decantation to obtain dispersion B. When the concentration of tin oxide powder in this dispersion B was measured, it was 2.8%. 200 parts of this dispersion B,
10 parts of ethyl silicate 40 and 280 parts of ethanol were mixed and stirred for 10 hours to obtain an inorganic conductive paint.
比較例
実施例1で使用したT−1,50部及びエタノール95
0部をホモミキサーで10時間分散させた。これを24
時間静置させると、殆ど全部のT1が沈殿し、上層は透
明な液となって、分散液ができなかった。そこで上記の
溶液を再度均一に分散させた後、沈殿を生成しないうち
に取り出した溶液100部とエチルシリケート40を1
2.5部及びエタノール200部を10時間混合撹拌し
て無機導電性塗料を得た。Comparative Example 50 parts of T-1 used in Example 1 and 95 ethanol
0 parts was dispersed in a homomixer for 10 hours. This is 24
When the mixture was allowed to stand for a period of time, almost all of the T1 precipitated, and the upper layer became a transparent liquid, making it impossible to form a dispersion. Therefore, after uniformly dispersing the above solution again, 100 parts of the solution taken out before precipitation was mixed with 100 parts of ethyl silicate 40.
2.5 parts and 200 parts of ethanol were mixed and stirred for 10 hours to obtain an inorganic conductive paint.
実施例1〜3及び比較例で得られた塗料の特性を第1表
に示す。Table 1 shows the properties of the paints obtained in Examples 1 to 3 and Comparative Examples.
第
表
実施例及び比較例の特性
:塗料を100dの三角フラスコに入れ密栓し、沈降の
有無を肉眼で観察して判定した。Properties of Examples and Comparative Examples in Table: The paint was placed in a 100 d Erlenmeyer flask and sealed tightly, and the presence or absence of sedimentation was determined by visual observation.
*2ニガラス基板に塗料をスピンコード(25Orpm
)後、80°Cで30分乾燥し、180″Cで60分の
条件で硬化させた。その試験片の表面抵抗を表面抵抗計
(横河ヒューレットバッカード製、ハイレジスタンスメ
ータ)を用いて測定した。*2 Spin code (25 Orpm) the paint on the glass substrate.
), then dried at 80°C for 30 minutes and cured at 180''C for 60 minutes.The surface resistance of the test piece was measured using a surface resistance meter (High Resistance Meter, manufactured by Yokogawa Hewlett Buckard). It was measured.
*3:*2で作成したガラス基板を分光光度計(日立製
作断裂150−20型ダブルビ一ム分光光度計)を用い
て、波長600nmの透過率を測定した。*3: The transmittance of the glass substrate prepared in *2 at a wavelength of 600 nm was measured using a spectrophotometer (Hitachi 150-20 Model Double Beam Spectrophotometer).
第1表に示されるように実施例の無機導電性塗料は沈降
性が良好で、導電性及び透明性が優れている。As shown in Table 1, the inorganic conductive paints of Examples have good sedimentation properties and excellent conductivity and transparency.
本発明の製法で得られる無機導電性塗料は、導電粉末の
沈降性が良好で、硬化塗膜の透明性及び導電性が優れ、
ガラス、プラスチックなどの透明基材の表面に塗布して
、基材に帯電防止効果を付与する用途などに好適である
。The inorganic conductive paint obtained by the manufacturing method of the present invention has good settling properties of the conductive powder, excellent transparency and conductivity of the cured coating film,
It is suitable for application to the surface of a transparent substrate such as glass or plastic to impart an antistatic effect to the substrate.
Claims (1)
下の酸化スズ粉末1〜10重量%、溶剤99〜90重量
%及びアンチモンがドープされた酸化スズ粉末の重量の
1〜10重量%の界面活性剤を分散機で分散させて沈殿
物を除去した後、(B)無機バインダー及び(C)溶剤
を添加混合することを特徴とする無機導電性塗料の製造
方法。 2、界面活性剤がカチオン系界面活性剤である請求項1
記載の無機導電性塗料の製造方法。[Claims] 1. (A) 1 to 10% by weight of antimony-doped tin oxide powder with a particle size of 0.2 μm or less, 99 to 90% by weight of a solvent, and the weight of antimony-doped tin oxide powder. A method for producing an inorganic conductive paint, which comprises dispersing 1 to 10% by weight of a surfactant using a dispersing machine to remove precipitates, and then adding and mixing (B) an inorganic binder and (C) a solvent. 2. Claim 1, wherein the surfactant is a cationic surfactant.
The method for producing the inorganic conductive paint described above.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2175290A JPH03227376A (en) | 1990-01-31 | 1990-01-31 | Production of inorganic electrically conductive coating material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2175290A JPH03227376A (en) | 1990-01-31 | 1990-01-31 | Production of inorganic electrically conductive coating material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03227376A true JPH03227376A (en) | 1991-10-08 |
Family
ID=12063796
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2175290A Pending JPH03227376A (en) | 1990-01-31 | 1990-01-31 | Production of inorganic electrically conductive coating material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03227376A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0688022A2 (en) * | 1991-03-27 | 1995-12-20 | Canon Kabushiki Kaisha | Optical modulation element |
EP0731487A1 (en) * | 1995-03-09 | 1996-09-11 | Chunghwa Picture Tubes, Ltd. | Antistatic coating for video display screen |
KR100786002B1 (en) * | 2004-06-30 | 2007-12-14 | 이 아이 듀폰 디 네모아 앤드 캄파니 | Thick-Film Conductor Paste |
-
1990
- 1990-01-31 JP JP2175290A patent/JPH03227376A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0688022A2 (en) * | 1991-03-27 | 1995-12-20 | Canon Kabushiki Kaisha | Optical modulation element |
EP0688022A3 (en) * | 1991-03-27 | 1996-07-17 | Canon Kk | Optical modulation element |
EP0731487A1 (en) * | 1995-03-09 | 1996-09-11 | Chunghwa Picture Tubes, Ltd. | Antistatic coating for video display screen |
KR100786002B1 (en) * | 2004-06-30 | 2007-12-14 | 이 아이 듀폰 디 네모아 앤드 캄파니 | Thick-Film Conductor Paste |
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