JPS5891777A - Electrically conductive clear paint - Google Patents
Electrically conductive clear paintInfo
- Publication number
- JPS5891777A JPS5891777A JP18898881A JP18898881A JPS5891777A JP S5891777 A JPS5891777 A JP S5891777A JP 18898881 A JP18898881 A JP 18898881A JP 18898881 A JP18898881 A JP 18898881A JP S5891777 A JPS5891777 A JP S5891777A
- Authority
- JP
- Japan
- Prior art keywords
- paint
- weight
- powder
- fine powder
- particle size
- 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.)
- Granted
Links
- 239000003973 paint Substances 0.000 title claims description 34
- 239000000843 powder Substances 0.000 claims description 31
- 239000002245 particle Substances 0.000 claims description 16
- 239000011347 resin Substances 0.000 claims description 10
- 229920005989 resin Polymers 0.000 claims description 10
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims description 8
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 3
- 229910052787 antimony Inorganic materials 0.000 claims description 2
- 229910001887 tin oxide Inorganic materials 0.000 claims description 2
- 238000000576 coating method Methods 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 230000001771 impaired effect Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000615 nonconductor Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- -1 polypropylene Polymers 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
- 150000001343 alkyl silanes Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- FAPDDOBMIUGHIN-UHFFFAOYSA-K antimony trichloride Chemical compound Cl[Sb](Cl)Cl FAPDDOBMIUGHIN-UHFFFAOYSA-K 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000007606 doctor blade method Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Conductive Materials (AREA)
- Non-Insulated Conductors (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
この発明は、透明にして導電性を有し、かつ帯電防止能
を有する塗布被膜を形成することのできる塗料に関する
ものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a coating material that is transparent, electrically conductive, and capable of forming a coating film having antistatic properties.
近年、IC保存用容器や、その他の電子電機部材、さら
にじゅうたん、床材、壁材などの建築用部材などで帯電
防止を必要とする場合が急増する傾向を見せ始めている
。また、マイクロ波による電磁波障害を防止するための
導電性塗料の要求も高まっている。In recent years, there has been a rapid increase in the number of cases in which static electricity prevention is required for IC storage containers, other electronic and electrical equipment components, and architectural components such as carpets, flooring materials, and wall materials. Additionally, there is an increasing demand for conductive paints to prevent electromagnetic interference caused by microwaves.
従来、このような要望に応えて、カーボン粉末や金属粉
末、あるいはカーボン繊維や金属繊維を混入して導電性
を持たせた塗料を塗布した9、アルキルアミンハロゲン
化物のようなイオン伝導性のある有機物を塗布して、不
導体に導電性を付与し、帯電を防止することが行なわれ
ていたが、前者にあっては塗布被膜のもつ色調が灰色ま
たは黒色がかったものになるため、不導体のもつ色調が
損なわれるようになって好ましくなく、また後者にあっ
ては塗布することによって透明な帯電防止能を有する被
膜を形成させることは可能であるが、湿度が高い状態で
ないと帯電防止の効果が得られず、しかも剥れやすいと
いう欠点を有していた。In the past, in response to these demands, paints containing conductive materials such as carbon powder, metal powder, or carbon fibers or metal fibers were applied. Organic substances have been applied to nonconductors to make them conductive and prevent static electricity, but in the former case, the color tone of the applied film becomes gray or blackish, so In the case of the latter, it is possible to form a transparent film with antistatic properties by coating, but the antistatic properties cannot be achieved unless the humidity is high. It had the disadvantage that it was not effective and was easy to peel off.
本発明者等は、上述のような観点から、塗布被膜自体が
下地の色調を損なうことのない透明性を有し、塗膜密着
性にもすぐれるとともに、良好な導電性を有しており、
不動体に塗布することによシ良好な導電性を付与し、か
つ十分な帯電防止能を発揮する塗料を得べく研究を重ね
た結果、(a)酸化錫(以下5nO7で示す)粉末は、
白色を呈し、かつ導電性を有するが、これにアンチモン
(sb)を含有させると、さらに一段と導電性が向上す
るようになシ、熱的にも安定したものであること。From the above-mentioned viewpoints, the present inventors have discovered that the coating film itself has transparency that does not impair the color tone of the base, has excellent coating film adhesion, and has good electrical conductivity. ,
As a result of repeated research to obtain a paint that imparts good conductivity and exhibits sufficient antistatic ability when applied to immovable objects, we have found that (a) tin oxide (hereinafter referred to as 5nO7) powder is
It is white in color and has electrical conductivity, but when antimony (sb) is added to it, the electrical conductivity is further improved, and it is also thermally stable.
(b) 粉末を混入させても塗料のもつ透明性や色調
が損なわれないようにするためには、混入する粉末が光
を吸収しない、すなわち白色を有し、かつその光屈折率
が塗料の主要素である樹脂の光屈折率:1.6〜1.7
に近いものであるか、あるいは粉末の平均粒径が0.4
μm以下、すなわち可視光の波長より小さく、光の散乱
が少ないことが必要であること。(b) In order to ensure that the transparency and color tone of the paint are not impaired even when the powder is mixed in, it is necessary that the powder to be mixed in does not absorb light, that is, it has a white color, and that its optical refractive index is the same as that of the paint. Optical refractive index of main element resin: 1.6-1.7
or the average particle size of the powder is 0.4
It must be smaller than μm, that is, smaller than the wavelength of visible light, and must have little light scattering.
(C)上記sbを含有したSnO2粉末は2.0〜2.
1の光屈折率を有しておシ、したがってこれを塗料に、
その色調、特に透明性を損なうことなく導電性を付与す
る目的で混入するに際しては、その平均粒径を0.4μ
m以下に微細化する必要があること。(C) The SnO2 powder containing the above sb is 2.0 to 2.0.
It has a light refractive index of 1, so it can be used as a paint.
When mixed for the purpose of imparting conductivity without impairing the color tone, especially transparency, the average particle size should be 0.4 μm.
It is necessary to miniaturize the size to less than m.
(d) 上記(C)項の平均粒径:0.4μm JJ
、下を有するsb含有5n02微粉末を塗料に混入する
に際しては、その混入量が塗料主要素たる樹脂との割合
で50重量%未満の場合には分散性よく均一に混入させ
ることができるのに対して、その混入量が同割合で50
重量%を越えると分散性が悪くなって均一混入が困難に
なるが、この場合には塗料への混入に先だって、前記微
粉末に、P H’7〜11に調整したアルカリ水溶液中
に所定時間分散保持の前処理を施してやると、前記微粉
末の塗料に対する分散性が著しく向上し、その混入量を
同割合で50重量%を越えて含有させても塗料中に均一
に分散するようになること。(d) Average particle size of item (C) above: 0.4 μm JJ
When mixing sb-containing 5N02 fine powder having the following properties into a paint, if the amount of the mixed powder is less than 50% by weight relative to the resin, which is the main component of the paint, it can be mixed uniformly with good dispersibility. On the other hand, the amount of contamination is 50% at the same ratio.
If it exceeds % by weight, the dispersibility deteriorates and it becomes difficult to mix uniformly, but in this case, before mixing into the paint, the fine powder is soaked in an alkaline aqueous solution adjusted to a pH of 7 to 11 for a predetermined period of time. When the pretreatment for maintaining dispersion is performed, the dispersibility of the fine powder in the paint is significantly improved, and even if the amount of the fine powder mixed exceeds 50% by weight at the same ratio, it will be uniformly dispersed in the paint. thing.
以上(a)〜(d)項に示される知見を得たのである。The findings shown in sections (a) to (d) above have been obtained.
この発明は、上記知見にもとづいてなされたものであっ
て、Sb:0.1〜20重量%を含有し、残りが実質的
に5n02からなる組成を有し、かつ0.4μm以下の
平均粒径を有する導電性微粉末を、前記導電性微粉末;
5〜90重量係重量係上塗料主要素脂:95〜10重量
%の割合で含有せしめることによって、良好な導電性と
帯電防止能を有し、かつ透明にして下地の色調に影響を
与えない塗布被膜を形成することのできる塗料とした点
に特徴を有するものである。This invention was made based on the above findings, and has a composition containing Sb: 0.1 to 20% by weight, with the remainder consisting essentially of 5n02, and having an average particle size of 0.4 μm or less. the conductive fine powder having a diameter;
5 to 90% by weightMain component of paint based on fat: By containing it at a ratio of 95 to 10% by weight, it has good conductivity and antistatic ability, and is transparent and does not affect the color tone of the base. It is characterized in that it is a paint that can form a coating film.
なお、一般の透明塗料では、塗料主要素たる樹脂として
は、アクリル系、ビニール系、カーボネート系、ポリエ
ステル系、ウレタン系、エポキシ系、およびポリプロピ
レン系などの樹脂が使用されているが、この発明の透明
塗料は、これらの透明塗料に上記導電性微粉末を所定量
含有させたものからなるのである。In addition, in general transparent paints, acrylic, vinyl, carbonate, polyester, urethane, epoxy, and polypropylene resins are used as the main component of the paint. The transparent paint is made of these transparent paints containing a predetermined amount of the above-mentioned conductive fine powder.
すなわち、この発明の透明塗料は、まず上記の樹脂ヲ、
アルコール、エステル、ケトン、エーテル、水などの溶
剤と混合し、さらにこれに上記導電性微粉末を添加混合
することによって製造されるが、この際、上記導電性微
粉末の分散性を高める目的で、リン酸ソーダ、スルホン
酸ソーダ、オレイン酸ソーダ、ステアリン酸ソーダ、ク
エン酸ソーダなどの陰イオン界面活性剤や、アルキルシ
5−
ラン、アルコキシシランなどのシランカップリング剤、
さらにアルキノビチタネート、アクリルチタネートなど
のチタネートカップリング剤を混合含有させてもよい。That is, the transparent paint of this invention first contains the above resin,
It is produced by mixing with a solvent such as alcohol, ester, ketone, ether, water, etc., and then adding and mixing the above-mentioned conductive fine powder. , anionic surfactants such as sodium phosphate, sodium sulfonate, sodium oleate, sodium stearate, and sodium citrate; silane coupling agents such as alkylsilane and alkoxysilane;
Furthermore, a titanate coupling agent such as alkynovititanate or acrylic titanate may be mixed and contained.
さらに、この発明の透明塗料は、一般の塗料塗布方法に
よって塗布することができるが、スプレー法、バーコー
ド法、およびドクターブレード法によって塗布を行なっ
た場合、良好な結果が得られる。Further, the transparent paint of the present invention can be applied by a general paint application method, but good results can be obtained when applied by a spray method, a bar code method, or a doctor blade method.
つぎに、この発明め透明塗料における導電性微粉末に関
し、sb含有量、平均粒径、および混入割合を上記の通
シに限定した理由を説明する。Next, the reason why the sb content, average particle size, and mixing ratio of the conductive fine powder in the transparent paint of the present invention are limited to the above-mentioned values will be explained.
(a) Sb含有量
その含有量が0.1重量%未満の場合には電気抵抗が高
く、所望の良好な導電性を確保できないので、帯電防止
能も十分でなく、一方20重量係を越えて含有した場合
には、微粉末の白色が失なわれて青味を帯びるようにな
り、塗料に混入した際に、その色調や透明性が損なわれ
るようになることから、その含有量を0.1〜20重量
%と限定し 6−
た。(a) Sb content If the Sb content is less than 0.1% by weight, the electrical resistance is high and the desired good conductivity cannot be secured, and the antistatic ability is also insufficient. If it is contained in the powder, the white color of the fine powder will be lost and it will become bluish, and when it is mixed into paint, the color tone and transparency will be impaired, so its content should be reduced to zero. The amount was limited to .1 to 20% by weight.
(1〕)平均粒径
その平均粒径が04μmを越えると、可視光の散乱が多
くなp1塗料中への混入に際して、その塗料のもつ透明
性が損なわれるようになるという理由から、0.4μm
以下の平均粒径とする必要がある。(1) Average particle size If the average particle size exceeds 0.4 μm, the transparency of the paint will be impaired when it is mixed into the P1 paint, which scatters a lot of visible light. 4μm
The average particle size must be as follows.
なお、この発明の透明塗料における導電性微粉末の平均
粒径は、まず内径:45mmを有する容量: 100
ccのポリエチレン製円筒状容器内に、前記微粉末:5
Iと、水:40ccを、直径:約10順の焼結アルミナ
ボール:50個と共に挿入し、この容器を40 Or、
p、mの回転数で10時間回転させた後、前記焼結アル
ミナボールを除いた内容物を遠心沈降器の容器に入れ、
遠心沈降器の回転数、回転時間を変えながら粉末を沈降
させ、それぞれ沈降した粉末の重量を測定し、この測定
結果に基づいて粒度分布を作成し、この粒度分布におけ
る50%の累積値をもって平均粒径とする方法によって
定めた。Incidentally, the average particle size of the conductive fine powder in the transparent paint of the present invention is as follows: First, the average particle size of the conductive fine powder in the transparent paint of this invention is as follows:
In a cc polyethylene cylindrical container, the fine powder: 5
I and 40 cc of water were inserted together with 50 sintered alumina balls of approximately 10 diameters, and the container was heated to 40 Or.
After rotating at a rotation speed of p and m for 10 hours, the contents except the sintered alumina balls were placed in a container of a centrifugal sedimentator,
The powder is sedimented while changing the rotation speed and rotation time of the centrifugal sedimentator, the weight of each sedimented powder is measured, a particle size distribution is created based on the measurement results, and the cumulative value of 50% of this particle size distribution is averaged. It was determined by the particle size method.
塗料の主要素たる樹脂に対する」−記微粉末の混入割合
が5重量係未満では、相対的に樹脂の割合が95重量%
を越えて高くなりすぎ、形成される塗膜の電気抵抗が高
く、所望の良好な導電性および帯電防止能が得られない
。一方、90重量%を越えると相対的に樹脂の割合が1
0重量%未満となって樹脂のもつ透明性が損なわれるよ
うになることから、その混入割合を導電性微粉末、5〜
90重量%、樹脂:95〜10重量%と定めた。If the proportion of the fine powder mixed with the resin, which is the main component of the paint, is less than 5% by weight, the relative proportion of the resin is 95% by weight.
If it becomes too high, the electrical resistance of the coating film formed is high, and the desired good conductivity and antistatic ability cannot be obtained. On the other hand, when it exceeds 90% by weight, the relative proportion of resin is 1
If the amount is less than 0% by weight, the transparency of the resin will be impaired.
90% by weight, resin: 95-10% by weight.
また、この発明の導電性微粉末は、アルコール。Moreover, the conductive fine powder of this invention is alcohol.
塩酸水溶液、およびアセトンの1種または2種以上の混
合液に塩化錫(以下5nC14で示す)と塩化アンチモ
ン(以下5bC43で示す)とを溶解したものからなる
溶液を、加熱水中に加えて、sb金含有SnO2を析出
させる方法によって製造することができる。なお、Sn
O2粉末とsb化合物とを焼成する方法や、Sn化合物
とsb化合物とを混合した後、焼成する方法などの公知
の方法によって製造されたsb含有5n02粉末は、い
ずれも0.4μmを越えた平均粒径をもつものであり、
したがって、これらの公知の方法では、この発明の0.
4μm以下の平均粒径を有する導電性微粉末を製造する
ことはできない。A solution of tin chloride (hereinafter referred to as 5nC14) and antimony chloride (hereinafter referred to as 5bC43) dissolved in one or more mixtures of hydrochloric acid and acetone is added to heated water, and sb It can be manufactured by a method of precipitating gold-containing SnO2. In addition, Sn
The sb-containing 5N02 powder manufactured by known methods such as the method of firing O2 powder and the sb compound, or the method of mixing the Sn compound and the sb compound and then firing, all have an average diameter exceeding 0.4 μm. It has a particle size,
Therefore, in these known methods, the 0.
It is not possible to produce conductive fine powder with an average particle size of 4 μm or less.
つぎに、この発明の導電性透明塗料を実施例により具体
的に説明する。Next, the conductive transparent paint of the present invention will be specifically explained with reference to Examples.
実施例
水: 3000 ccを、温度:90℃に加熱保持し、
これに激しく攪拌を加えながら、それぞれ第1表に示さ
れる]゛のアルコール、塩酸水溶液、およびアセトンの
1種または2種以上からなる溶液に同じく第1表に示さ
れる量゛の8nC14と5bcz、とをそれぞれ溶解し
たものからなる溶液を、4時間かけてゆっくりと注入し
てsb含有5n02粉末を析出生成せしめ、ついで前記
sb含有SnO2粉末をF別し、洗浄し、引き続いて結
晶性を向上させる目的で、空気中、温度:500℃に2
時間保持の加熱処理を施し、この結果得られた導電性微
粉末に対して、第1表に示される条件で前処理を施した
後、同じく第1表に示される塗料配合組成に配合し、1
09−
時間混合することによって本発明塗料1〜5をそれぞれ
製造した。Example water: 3000 cc was heated and maintained at a temperature of 90°C,
While vigorously stirring, 8nC14 and 5bcz in the amounts also shown in Table 1 were added to a solution consisting of one or more of alcohol, hydrochloric acid aqueous solution, and acetone respectively shown in Table 1. and are slowly injected over a period of 4 hours to precipitate sb-containing 5N02 powder, and then the sb-containing SnO2 powder is separated by F, washed, and subsequently improved in crystallinity. In the air, at a temperature of 500°C.
The conductive fine powder obtained as a result of time-holding heat treatment is subjected to pretreatment under the conditions shown in Table 1, and then blended into the paint composition shown in Table 1, 1
Coatings according to the invention 1 to 5 were each prepared by mixing for 09- hours.
つぎに、この結果得られた本発明塗料1〜5を、第1表
に示される不導体の表面に同じく第1表に示される厚さ
に塗布し、この結果の塗膜の表面抵抗を測定すると共に
、その性状を観察した。Next, the resulting paints 1 to 5 of the present invention were applied to the surface of the nonconductor shown in Table 1 to a thickness also shown in Table 1, and the surface resistance of the resulting coating film was measured. At the same time, we observed its properties.
第1表に示される結果から、本発明塗料1〜5は、いず
れもすぐれた導電性を有し、したがってすぐれた帯電防
止能を有し、かつ不導体のもつ色調を損なうことのない
塗布被膜を形成することができるものであることが明ら
かである。From the results shown in Table 1, it can be seen that coatings 1 to 5 of the present invention all have excellent conductivity and therefore have excellent antistatic ability, and can form coatings that do not impair the color tone of the nonconductor. It is clear that it is possible to form a
」一連のように、この発明の塗料は、すぐれた導電性、
並びに帯電防止能を有し、かつ下地の色調を損なうこと
の少ない透明性を有する塗布被膜を形成することができ
、したがって、これを電子電機部材や建築用部材などの
帯電防止や、電磁波の遮蔽などに用いた場合著しくすぐ
れた性能を発揮するのである。”As in the series, the paint of this invention has excellent conductivity,
In addition, it is possible to form a coating film that has antistatic ability and transparency that does not impair the color tone of the base material. When used in applications such as this, it exhibits extremely superior performance.
出願人 三菱金属株式会社 代理人 富 1) 和 夫 11−Applicant: Mitsubishi Metals Corporation Agent Tomi 1) Kazuo 11-
Claims (1)
的に酸化錫からなる組成を有し、かつ0.4μm以下の
平均粒径をもった導電性微粉末を、前記導電性微粉末:
5〜90重量%、塗料主要素たる樹脂:95〜10重量
%の割合で含有することを特徴とする導電性透明塗料。A conductive fine powder containing 0.1 to 20% by weight of antimony, with the remainder substantially consisting of tin oxide, and having an average particle size of 0.4 μm or less is used as the conductive fine powder. :
A conductive transparent paint characterized by containing 5 to 90% by weight of resin, which is a main component of the paint, and 95 to 10% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18898881A JPS5891777A (en) | 1981-11-25 | 1981-11-25 | Electrically conductive clear paint |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18898881A JPS5891777A (en) | 1981-11-25 | 1981-11-25 | Electrically conductive clear paint |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5891777A true JPS5891777A (en) | 1983-05-31 |
JPS6313463B2 JPS6313463B2 (en) | 1988-03-25 |
Family
ID=16233417
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18898881A Granted JPS5891777A (en) | 1981-11-25 | 1981-11-25 | Electrically conductive clear paint |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5891777A (en) |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59122561A (en) * | 1982-12-28 | 1984-07-16 | Mitsubishi Metal Corp | Conductive transparent paint that is stable against moisture |
JPS606454A (en) * | 1983-06-24 | 1985-01-14 | タキロン株式会社 | Antistatic plastic composite sheet |
JPS6060166A (en) * | 1983-09-13 | 1985-04-06 | Sekisui Chem Co Ltd | Photocurable electrically conductive paint composition |
JPS60118765A (en) * | 1983-11-29 | 1985-06-26 | Matsushita Electric Ind Co Ltd | Photosensitive conductive coating |
JPS60181172A (en) * | 1984-02-29 | 1985-09-14 | Sekisui Chem Co Ltd | Antistatic transparent coating compound |
JPS60181177A (en) * | 1984-02-29 | 1985-09-14 | Sekisui Chem Co Ltd | Electrically-conductive coating compound composition, electrically-conductive plastic sheet or plate using it |
JPS60229964A (en) * | 1984-04-27 | 1985-11-15 | Sekisui Chem Co Ltd | Paint for antistatic use |
JPS60243166A (en) * | 1984-05-17 | 1985-12-03 | Sekisui Chem Co Ltd | Antistatic clear coating |
JPS60245675A (en) * | 1984-05-21 | 1985-12-05 | Sekisui Chem Co Ltd | Antistatic paint |
JPS619464A (en) * | 1984-06-22 | 1986-01-17 | Sekisui Chem Co Ltd | Antistatic paint |
JPS6147738A (en) * | 1984-08-14 | 1986-03-08 | Sekisui Chem Co Ltd | Transparent antistatic film or sheet |
JPS61264069A (en) * | 1985-05-17 | 1986-11-21 | Matsushita Electric Ind Co Ltd | Coating material for resistance |
JPS62273270A (en) * | 1986-05-21 | 1987-11-27 | Nissan Chem Ind Ltd | Electrically conductive inorganic coating agent and its production |
JPS62278705A (en) * | 1986-05-26 | 1987-12-03 | 多木化学株式会社 | Transparent conducting material |
JPS6323965A (en) * | 1986-07-16 | 1988-02-01 | Kuraray Co Ltd | Electrically conductive organic composition |
JPS6346274A (en) * | 1986-08-12 | 1988-02-27 | Catalysts & Chem Ind Co Ltd | Electrically conductive coating material |
JPS6366267A (en) * | 1986-09-05 | 1988-03-24 | Honny Chem Ind Co Ltd | Transparent electrically conductive coating agent for plasticized flexible polyvinyl chloride |
JPS63314709A (en) * | 1987-06-17 | 1988-12-22 | Matsushita Electric Ind Co Ltd | Transparent electricity conductive film |
JPH0354266A (en) * | 1989-07-24 | 1991-03-08 | Daicel Chem Ind Ltd | Antistatic coating material |
US6143418A (en) * | 1996-06-11 | 2000-11-07 | Sumitomo Osaka Cement Co., Ltd. | Transparent conductive film, low-reflectivity transparent conductive film, and display device |
WO2013147029A1 (en) | 2012-03-29 | 2013-10-03 | 三菱マテリアル株式会社 | Antimony-doped tin oxide powder and process for manufacturing same |
WO2013147033A1 (en) * | 2012-03-29 | 2013-10-03 | 三菱マテリアル株式会社 | Infrared cut material |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0559651U (en) * | 1991-12-27 | 1993-08-06 | 株式会社三協精機製作所 | Rotational position detector |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5061435A (en) * | 1973-10-02 | 1975-05-27 | ||
JPS56143443A (en) * | 1980-04-11 | 1981-11-09 | Fuji Photo Film Co Ltd | Electrically conductive support for electrophotographic material |
-
1981
- 1981-11-25 JP JP18898881A patent/JPS5891777A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5061435A (en) * | 1973-10-02 | 1975-05-27 | ||
JPS56143443A (en) * | 1980-04-11 | 1981-11-09 | Fuji Photo Film Co Ltd | Electrically conductive support for electrophotographic material |
Cited By (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59122561A (en) * | 1982-12-28 | 1984-07-16 | Mitsubishi Metal Corp | Conductive transparent paint that is stable against moisture |
JPH0458511B2 (en) * | 1982-12-28 | 1992-09-17 | Mitsubishi Materiaru Kk | |
JPS606454A (en) * | 1983-06-24 | 1985-01-14 | タキロン株式会社 | Antistatic plastic composite sheet |
JPS634796B2 (en) * | 1983-06-24 | 1988-01-30 | Takiron Co | |
JPS6060166A (en) * | 1983-09-13 | 1985-04-06 | Sekisui Chem Co Ltd | Photocurable electrically conductive paint composition |
JPS6355550B2 (en) * | 1983-09-13 | 1988-11-02 | Sekisui Chemical Co Ltd | |
JPS60118765A (en) * | 1983-11-29 | 1985-06-26 | Matsushita Electric Ind Co Ltd | Photosensitive conductive coating |
JPH0535190B2 (en) * | 1983-11-29 | 1993-05-25 | Matsushita Electric Ind Co Ltd | |
JPH0549713B2 (en) * | 1984-02-29 | 1993-07-27 | Sekisui Chemical Co Ltd | |
JPS60181177A (en) * | 1984-02-29 | 1985-09-14 | Sekisui Chem Co Ltd | Electrically-conductive coating compound composition, electrically-conductive plastic sheet or plate using it |
JPS60181172A (en) * | 1984-02-29 | 1985-09-14 | Sekisui Chem Co Ltd | Antistatic transparent coating compound |
JPS60229964A (en) * | 1984-04-27 | 1985-11-15 | Sekisui Chem Co Ltd | Paint for antistatic use |
JPS60243166A (en) * | 1984-05-17 | 1985-12-03 | Sekisui Chem Co Ltd | Antistatic clear coating |
JPS60245675A (en) * | 1984-05-21 | 1985-12-05 | Sekisui Chem Co Ltd | Antistatic paint |
JPS619464A (en) * | 1984-06-22 | 1986-01-17 | Sekisui Chem Co Ltd | Antistatic paint |
JPH0449857B2 (en) * | 1984-08-14 | 1992-08-12 | Sekisui Chemical Co Ltd | |
JPS6147738A (en) * | 1984-08-14 | 1986-03-08 | Sekisui Chem Co Ltd | Transparent antistatic film or sheet |
JPS61264069A (en) * | 1985-05-17 | 1986-11-21 | Matsushita Electric Ind Co Ltd | Coating material for resistance |
JPS62273270A (en) * | 1986-05-21 | 1987-11-27 | Nissan Chem Ind Ltd | Electrically conductive inorganic coating agent and its production |
JPH0588875B2 (en) * | 1986-05-21 | 1993-12-24 | Nissan Chemical Ind Ltd | |
JPH0586605B2 (en) * | 1986-05-26 | 1993-12-13 | Taki Chemical | |
JPS62278705A (en) * | 1986-05-26 | 1987-12-03 | 多木化学株式会社 | Transparent conducting material |
JPS6323965A (en) * | 1986-07-16 | 1988-02-01 | Kuraray Co Ltd | Electrically conductive organic composition |
JPH0619074B2 (en) * | 1986-08-12 | 1994-03-16 | 触媒化成工業株式会社 | Conductive paint |
JPS6346274A (en) * | 1986-08-12 | 1988-02-27 | Catalysts & Chem Ind Co Ltd | Electrically conductive coating material |
JPS6366267A (en) * | 1986-09-05 | 1988-03-24 | Honny Chem Ind Co Ltd | Transparent electrically conductive coating agent for plasticized flexible polyvinyl chloride |
JPS63314709A (en) * | 1987-06-17 | 1988-12-22 | Matsushita Electric Ind Co Ltd | Transparent electricity conductive film |
JPH0354266A (en) * | 1989-07-24 | 1991-03-08 | Daicel Chem Ind Ltd | Antistatic coating material |
US6143418A (en) * | 1996-06-11 | 2000-11-07 | Sumitomo Osaka Cement Co., Ltd. | Transparent conductive film, low-reflectivity transparent conductive film, and display device |
WO2013147029A1 (en) | 2012-03-29 | 2013-10-03 | 三菱マテリアル株式会社 | Antimony-doped tin oxide powder and process for manufacturing same |
WO2013147033A1 (en) * | 2012-03-29 | 2013-10-03 | 三菱マテリアル株式会社 | Infrared cut material |
JP5798240B2 (en) * | 2012-03-29 | 2015-10-21 | 三菱マテリアル電子化成株式会社 | Antimony-doped tin oxide powder and method for producing the same |
US9513408B2 (en) | 2012-03-29 | 2016-12-06 | Mitsubishi Materials Corporation | Antimony-doped tin oxide powder and method of producing the same |
Also Published As
Publication number | Publication date |
---|---|
JPS6313463B2 (en) | 1988-03-25 |
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