JP3357107B2 - White conductive titanium dioxide powder and method for producing the same - Google Patents

White conductive titanium dioxide powder and method for producing the same

Info

Publication number
JP3357107B2
JP3357107B2 JP00335593A JP335593A JP3357107B2 JP 3357107 B2 JP3357107 B2 JP 3357107B2 JP 00335593 A JP00335593 A JP 00335593A JP 335593 A JP335593 A JP 335593A JP 3357107 B2 JP3357107 B2 JP 3357107B2
Authority
JP
Japan
Prior art keywords
titanium dioxide
white conductive
producing
dioxide powder
inert gas
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP00335593A
Other languages
Japanese (ja)
Other versions
JPH06207118A (en
Inventor
昭洋 好本
俊宏 好永
茂 長岡
正育 森下
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.)
Titan Kogyo KK
Original Assignee
Titan Kogyo KK
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 Titan Kogyo KK filed Critical Titan Kogyo KK
Priority to JP00335593A priority Critical patent/JP3357107B2/en
Publication of JPH06207118A publication Critical patent/JPH06207118A/en
Application granted granted Critical
Publication of JP3357107B2 publication Critical patent/JP3357107B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09CTREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C1/00Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/36Compounds of titanium
    • C09C1/3607Titanium dioxide
    • C09C1/3653Treatment with inorganic compounds
    • C09C1/3661Coating

Description

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

【0001】[0001]

【産業上の利用分野】本発明は帯電防止用の塗料、プラ
スチック、繊維等に用いられる白色導電性二酸化チタン
粉末に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a white conductive titanium dioxide powder used for antistatic paints, plastics, fibers and the like.

【0002】[0002]

【従来の技術】現在、導電材料として多量に使用されて
いるカーボンブラックや金属粉は、電気抵抗が非常に低
く、特性的には優れているものの、それらの色調が黒色
のため用途が限定されていた。その対策として、二酸化
チタンの表面を、酸化スズで被覆したもの(特開昭53
−92854公報)やその導電性改良品としてアンチモ
ンをドープした酸化スズを被覆した白色の導電性酸化チ
タンの製造法が開示された(特開昭58−209002
公報など)。
2. Description of the Related Art At present, carbon black and metal powder, which are used in large amounts as conductive materials, have very low electric resistance and excellent characteristics, but their color tone is black, so their use is limited. I was As a countermeasure, a titanium dioxide surface coated with tin oxide (Japanese Patent Laid-Open No.
Japanese Unexamined Patent Publication (Kokai) No. 58-209002) and a method for producing white conductive titanium oxide coated with antimony-doped tin oxide as an improved conductivity thereof.
Gazettes).

【0003】この白色導電性酸化チタンを用いた、帯電
防止用の塗料、プラスチック、繊維は、白色という利点
を生かし、清潔感を必要とする白衣やクリーンルームの
内装あるいは明彩色の塗料やプラスチック製品に近年需
要を増してきている。
[0003] Antistatic paints, plastics and fibers using this white conductive titanium oxide take advantage of the white color and can be used in white coats and clean room interiors or in brightly colored paints and plastic products that require a clean feeling. In recent years, demand has been increasing.

【0004】しかしながら、最近アンチモンの毒性上の
問題が取沙汰されるようになり、アンチモンを含有しな
い白色導電性酸化チタン粉末の開発が必要となった。ア
ンチモンを使用しない製法として、例えば特開平4−1
54621公報が開示されたが、この方法ではアンチモ
ンを含有しないものの電気抵抗がアンチモンを含有した
ものと同等のものは得られていない。
[0004] However, recently, the problem of antimony toxicity has been raised, and it has become necessary to develop a white conductive titanium oxide powder containing no antimony. As a production method using no antimony, for example, Japanese Patent Laid-Open No. 4-1
No. 54621 was disclosed, but this method did not contain antimony, but did not obtain an electrical resistance equivalent to that containing antimony.

【0005】[0005]

【発明が解決しようとする課題】本発明は毒性のあるア
ンチモンを使用しないにもかかわらず、白度が高く、か
つ優れた導電性を有する、白色導電性二酸化チタン粉末
を提供しようとするものである。
DISCLOSURE OF THE INVENTION The present invention aims to provide a white conductive titanium dioxide powder having high whiteness and excellent conductivity even though toxic antimony is not used. is there.

【0006】[0006]

【課題を解決するための手段】本発明者らは白度を保ち
ながら、かつ毒性上の問題のあるアンチモンを使用しな
いにもかかわらず、アンチモン含有品と同等の導電性を
有する酸化チタン粉末を開発する為鋭意研究を重ねた結
果、本発明を完成したものである。すなわち、本発明
は、二酸化チタン粒子表面に、リンを0.1〜10重量
%含む酸化スズの被覆層を有することを特徴とする白色
導電性二酸化チタン粉末を提供するものである。
DISCLOSURE OF THE INVENTION The present inventors have developed a titanium oxide powder having the same conductivity as an antimony-containing product while maintaining whiteness and not using antimony which has a toxicity problem. As a result of intensive research for development, the present invention has been completed. That is, the present invention provides a white conductive titanium dioxide powder having a tin oxide coating layer containing 0.1 to 10% by weight of phosphorus on the surface of titanium dioxide particles.

【0007】本発明にかかる白色導電性二酸化チタン粉
末は、二酸化チタン粒子表面へスズの加水反応生成物を
均一に沈着させ、その後リンを酸化スズに対し0.1〜
10重量%被覆させることによる製造することができ
る。さらに非酸化性雰囲気にて500〜800℃で加熱
処理することが好ましく、該加熱処理は不活性ガスを吹
き込みながら行う事がより好ましい。
[0007] The white conductive titanium dioxide powder according to the present invention uniformly deposits a reaction product of tin on the surface of titanium dioxide particles, and then transfers phosphorus to tin oxide in an amount of 0.1 to 0.1%.
It can be produced by coating 10% by weight. Further, heat treatment is preferably performed at 500 to 800 ° C. in a non-oxidizing atmosphere, and more preferably, the heat treatment is performed while blowing an inert gas.

【0008】本発明の基体となる二酸化チタンとして
は、球状、針状などの様な形状のものも使用することが
できる。また、結晶形としては、アナターゼ型、ルチル
型及び非晶質のものも使用することができる。また、二
酸化チタンのアルカリ金属化合物、例えば、チタン酸カ
リウムやチタン酸ナトリウムなども使用することができ
る。
[0008] As the titanium dioxide serving as the substrate of the present invention, those having a shape such as a sphere or a needle can be used. As the crystalline form, anatase type, rutile type and amorphous type can also be used. Further, an alkali metal compound of titanium dioxide, for example, potassium titanate or sodium titanate can also be used.

【0009】酸化スズの水和物の被膜を形成させる方法
としては、種々の方法がある。例えば、二酸化チタンの
水懸濁液に、スズ塩またはスズ酸塩の溶液を添加した
後、アルカリまたは酸を添加する方法、スズ塩またはス
ズ酸塩とアルカリまたは酸とを別々に並行して添加し被
覆処理する方法等がある。二酸化チタン粒子表面に酸化
スズの含水物を均一に被覆処理するには、後者の並行添
加の方法がより適しており、この時、水懸濁液を50〜
100℃に加温保持することがより好ましい。又、スズ
塩またはスズ酸塩とアルカリまたは酸とを並行添加する
際のpHを2〜9とし、酸化チタン及び水酸化スズの等
電点より、好ましくはpH=2〜3あるいはpH6.5
〜8.5で維持することが重要で、これによりスズの加
水反応生成物を二酸化チタン粒子表面に均一に沈着させ
ることができる。
There are various methods for forming a hydrated film of tin oxide. For example, a method of adding an alkali or acid after adding a tin salt or stannate solution to an aqueous suspension of titanium dioxide, separately adding a tin salt or stannate and an alkali or acid separately and in parallel And a coating method. In order to uniformly coat the surface of the titanium dioxide particles with the hydrated tin oxide, the latter method of parallel addition is more suitable.
It is more preferable to keep the temperature at 100 ° C. When the tin salt or stannate and the alkali or acid are added in parallel, the pH is adjusted to 2 to 9, and the isoelectric point of titanium oxide and tin hydroxide is preferably pH = 2 to 3 or pH 6.5.
It is important to keep it at ~ 8.5, so that the reaction product of tin can be uniformly deposited on the surface of the titanium dioxide particles.

【0010】スズ塩としては、例えば、塩化スズ、硫酸
スズ、硝酸スズ等を使用することができる。また、スズ
酸塩としては、例えば、スズ酸ナトリウム、スズ酸カリ
ウム等を使用することができる。
As the tin salt, for example, tin chloride, tin sulfate, tin nitrate and the like can be used. Further, as the stannate, for example, sodium stannate, potassium stannate and the like can be used.

【0011】アルカリとしては、例えば、水酸化ナトリ
ウム、水酸化カリウム、炭酸ナトリウム、炭酸カリウ
ム、炭酸アンモニウム、アンモニア水、アンモニアガス
等、酸としては、例えば、塩酸、硫酸、硝酸、酢酸等を
使用することができる。
As the alkali, for example, sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, ammonium carbonate, aqueous ammonia, ammonia gas and the like are used. As the acid, for example, hydrochloric acid, sulfuric acid, nitric acid, acetic acid and the like are used. be able to.

【0012】酸化スズの被覆量は基体顔料に対してSn
2として5〜100重量%が好ましく、さらに好まし
くは10〜50重量%である。少な過ぎると所望の導電
性が得がたく、多過ぎると被覆が不均一になりやすく、
白度が低下する恐れがある。
The coating amount of tin oxide is Sn
O 2 is preferably 5 to 100% by weight, more preferably 10 to 50% by weight. If the amount is too small, it is difficult to obtain the desired conductivity, and if the amount is too large, the coating tends to be uneven,
The whiteness may decrease.

【0013】リンの処理方法としては、例えば、あらか
じめ、スズ塩あるいはスズ酸塩の溶液に溶解しておき、
酸化スズの含水物と同時に被膜層を形成する方法、酸化
スズの含水物の被膜を形成した後に添加する方法等があ
る。酸化スズの含水物の被覆をより均一に形成するに
は、後者の方がより好ましい。
As a method for treating phosphorus, for example, a method of dissolving in a tin salt or a stannate solution in advance is used.
There are a method of forming a film layer simultaneously with the hydrated tin oxide and a method of adding the film after forming a film of the hydrated tin oxide. In order to form a coating of a hydrated tin oxide more uniformly, the latter is more preferable.

【0014】リンの原料としては、例えば、オルトリン
酸、メタリン酸、ピロリン酸、トリポリリン酸、亜リン
酸、次亜リン酸およびこれらのアンモニウム塩、ナトリ
ウム塩、カリウム塩等を使用することができる。
As a raw material of phosphorus, for example, orthophosphoric acid, metaphosphoric acid, pyrophosphoric acid, tripolyphosphoric acid, phosphorous acid, hypophosphorous acid, and ammonium salts, sodium salts and potassium salts thereof can be used.

【0015】リンの添加量はSnO2に対して、Pとして
0.1〜10重量%、好ましくは0.3〜5重量%であ
り、少な過ぎると所望の導電性が得られず、多過ぎると
酸化スズの結晶性が悪くなり、所望の導電性が得られな
い。かかる量のリンを添加することにより、無添加のも
のに比べ電気抵抗を更に1/10〜1/20程度低くす
ることができることが本発明の特徴である。
The amount of phosphorus added is 0.1 to 10% by weight, preferably 0.3 to 5% by weight, as P, based on SnO 2. If the amount is too small, the desired conductivity cannot be obtained, and the amount is too large. In addition, the crystallinity of tin oxide deteriorates, and the desired conductivity cannot be obtained. It is a feature of the present invention that by adding such an amount of phosphorus, the electric resistance can be further reduced by about 1/10 to 1/20 as compared with the case where no phosphorus is added.

【0016】なお、本明細書において、「導電性」粉末
とは、粉体の電気比抵抗値として1〜500Ω・cmの
値を有するものを意味する。後述の実施例においても示
されるように、本発明により100Ω・cm以下という
良好な値を有する二酸化チタン粉末を得ることができ
る。
In the present specification, "conductive" powder means a powder having an electric resistivity of 1 to 500 Ω · cm. As will be shown in Examples described later, a titanium dioxide powder having a favorable value of 100 Ω · cm or less can be obtained by the present invention.

【0017】加熱処理を行う際には、500〜800℃
で非酸化性雰囲気にて行うことが好ましく、空気中で加
熱処理したものと比べ粉体の電気抵抗を少なくとも3桁
以上、場合により4桁低くすることができる。非酸化性
雰囲気とするためには、不活性ガスあるいは、還元性ガ
スが使用できる。不活性ガスとしては例えば、窒素、ヘ
リウム、アルゴン、炭酸ガス等を使用することができ
る。還元性ガスとしては、例えば、水素、アンモニア、
一酸化炭素等を使用することができる。好ましくは、窒
素ガスなどの不活性ガスを1〜10リットル/分程度吹
き込みながら加熱処理を行うことにより、性状の安定し
たものが得られる。
When the heat treatment is performed, the temperature is 500 to 800 ° C.
Is preferably performed in a non-oxidizing atmosphere, and the electrical resistance of the powder can be reduced by at least three digits or more, and in some cases, four orders of magnitude, as compared with the case where the powder is heat-treated in air. In order to obtain a non-oxidizing atmosphere, an inert gas or a reducing gas can be used. As the inert gas, for example, nitrogen, helium, argon, carbon dioxide, or the like can be used. Examples of the reducing gas include hydrogen, ammonia,
Carbon monoxide or the like can be used. Preferably, by performing a heat treatment while blowing an inert gas such as a nitrogen gas at a rate of about 1 to 10 liter / minute, a substance having a stable property can be obtained.

【0018】加熱する際の温度は500〜800℃が好
ましく、この範囲より低い場合にはさして導電性の向上
がみられず、高い場合には焼結等の問題が起こる恐れが
ある。又、加熱時間は、短かすぎる場合には加熱効果が
なく、長すぎてもそれ以上の効果が望めないことから、
15分〜4時間程度が適当であり、好ましくは、1〜2
時間程度である。
The temperature at the time of heating is preferably 500 to 800 ° C. If the temperature is lower than this range, no further improvement in conductivity is observed. If the temperature is higher, problems such as sintering may occur. In addition, the heating time is too short, there is no heating effect, too long because no further effect can be expected,
About 15 minutes to 4 hours is appropriate, preferably 1 to 2 hours.
About an hour.

【0019】以下に実施例を挙げて本発明をさらに詳細
に説明する。以下の実施例は単に例示の為に記すもので
あり、発明の範囲がこれらによって制限されるものでは
ない。
Hereinafter, the present invention will be described in more detail with reference to examples. The following examples are provided for illustrative purposes only, and are not intended to limit the scope of the invention.

【0020】実施例1 平均粒径0.22μmのルチル型二酸化チタン粉末30
0gを水3リットルに分散させて水懸濁液とした。この
懸濁液を70℃に加温保持した。別途用意した、塩化第
二スズ(SnCl4・5H2O 98重量%)160.5gを
2N塩酸1.5リットルに溶かした溶液と12重量%ア
ンモニア水とを、懸濁液のpHを7〜8に保持する様に
約2時間かけて、同時滴下した。さらに、オルトリン酸
1.1gを水10ミリリットルに溶解した水溶液を添加
した後、30分間撹拌し、二酸化チタン粒子表面にリン
を含んだ酸化スズの含水物を被覆処理し、処理懸濁液を
濾過、洗浄し、得られた処理二酸化チタンのケーキを1
10℃で乾燥した。次いで、得られた乾燥粉末を窒素ガ
ス気流中(3リットル/分)で650℃で1時間熱処理
して、目的とする白色導電性二酸化チタン粉末を得た。
Example 1 Rutile-type titanium dioxide powder 30 having an average particle size of 0.22 μm
0 g was dispersed in 3 liters of water to obtain an aqueous suspension. This suspension was kept warm at 70 ° C. Separately prepared, and a solution with 12 wt% ammonia water prepared by dissolving stannic chloride (SnCl 4 · 5H 2 O 98% by weight) 160.5 g of 2N hydrochloric acid 1.5 liters 7 the pH of the suspension The mixture was dropped simultaneously over about 2 hours so as to keep the temperature at 8. Further, after adding an aqueous solution in which 1.1 g of orthophosphoric acid is dissolved in 10 ml of water, the mixture is stirred for 30 minutes, the surface of the titanium dioxide particles is coated with a hydrate of tin oxide containing phosphorus, and the treated suspension is filtered. , Washed and the resulting treated titanium dioxide cake in 1
Dried at 10 ° C. Next, the obtained dry powder was heat-treated at 650 ° C. for 1 hour in a nitrogen gas stream (3 L / min) to obtain a target white conductive titanium dioxide powder.

【0021】実施例2 実施例1において、塩化第二スズ160.5gの代わり
に、244.2g、オルトリン酸1.1gの代わりに1.
7gを用いたことのほかは同例の場合と同様に処理し
て、目的とする白色導電性二酸化チタン粉末を得た。
Example 2 In Example 1, 244.2 g was used instead of 160.5 g of stannic chloride, and 1.1 g instead of 1.1 g of orthophosphoric acid.
Except for using 7 g, the same treatment as in the same example was carried out to obtain a target white conductive titanium dioxide powder.

【0022】実施例3 実施例1においてオルトリン酸1.1gの代わりに6.6
gを用いたことのほかは同例の場合と同様に処理した。
Example 3 In Example 1, instead of 1.1 g of orthophosphoric acid, 6.6 was used.
Except for using g, the treatment was the same as in the same example.

【0023】実施例4 実施例2においてオルトリン酸1.7gの代わりに5.4
gを用いたことのほかは同例の場合と同様に処理した。
Example 4 In Example 2, 5.4 g of orthophosphoric acid was used instead of 1.7 g of orthophosphoric acid.
Except for using g, the treatment was the same as in the same example.

【0024】比較例1 オルトリン酸を添加しないことのほかは、実施例1と同
様に処理した。
Comparative Example 1 The procedure of Example 1 was repeated except that orthophosphoric acid was not added.

【0025】比較例2 オルトリン酸を添加しないことのほかは、実施例2と同
様に処理した。
Comparative Example 2 The procedure of Example 2 was repeated except that orthophosphoric acid was not added.

【0026】粉体の電気比抵抗の測定 前記の実施例および比較例で得られた各粉末試料を23
0kg/cm2の圧力の加圧成形した状態(直径25.4
mm、厚さ3.3mm)での電気抵抗を横河−ヒューレ
ット・パッカード社製デジタルLCRメータ4261A
にて測定し、比抵抗に換算した。これらの結果を表1に
示す。
Measurement of Electric Resistivity of Powder Each powder sample obtained in the above Examples and Comparative Examples was
0 kg / cm 2 pressure molded state (diameter 25.4)
mm, thickness 3.3 mm) by using a digital LCR meter 4261A manufactured by Yokogawa-Hewlett-Packard Company.
And converted to specific resistance. Table 1 shows the results.

【0027】[0027]

【表1】 表1 酸化スズ被覆量 リン被覆量 加熱処理 粉体の電気比抵抗 (重量%) P/SnO2(重量%) (650℃,1時間) (Ω・cm) 実施例1 23 0.5 窒素中 29 実施例2 35 0.5 〃 90 実施例3 23 3 〃 33 実施例4 35 3 〃 87 比較例1 23 0 〃 633 比較例2 35 0 〃 2200Table 1 Tin oxide coating amount Phosphorous coating amount Heat treatment Electrical resistivity of powder (% by weight) P / SnO 2 (% by weight) (650 ° C., 1 hour) (Ω · cm) Example 1 230 2.5 in nitrogen 29 Example 2 35 0.5 90 90 Example 3 233 33 33 Example 4 353 87 87 Comparative Example 1 230 〃 633 Comparative Example 2 350 〃 2200

【0028】[0028]

【発明の効果】本発明は毒性上の問題のあるアンチモン
を使用することなく種々の分野に利用できる導電性に優
れた白色度の高い導電性二酸化チタン粉末を、比較的容
易に製造するものであり、工業的に高い利点がある。
According to the present invention, conductive titanium dioxide powder having high conductivity and high whiteness, which can be used in various fields without using antimony which has a toxicity problem, can be produced relatively easily. Yes, there are high industrial advantages.

フロントページの続き (72)発明者 森下 正育 山口県宇部市大字小串1978番地の25 チ タン工業株式会社内 (56)参考文献 特開 昭58−209002(JP,A) 特開 平4−154621(JP,A) 特開 昭63−11519(JP,A) 特開 昭64−54613(JP,A) 特開 平4−363366(JP,A) 特開 平5−262526(JP,A) 特開 平6−183708(JP,A) (58)調査した分野(Int.Cl.7,DB名) C09C 1/00 - 3/12 C01G 23/00 - 23/08 H01B 1/00 - 1/24 C09D 5/24 C08K 3/00 - 3/40 C08K 9/02 Continuing from the front page (72) Inventor Masayuki Morishita Inside of 25 Titan Kogyo Co., Ltd. at 1978 Kogushi, Ube City, Yamaguchi Prefecture (56) References JP-A-58-209002 (JP, A) JP-A-4-154621 (JP, A) JP-A-63-11519 (JP, A) JP-A-64-54613 (JP, A) JP-A-4-363366 (JP, A) JP-A-5-262526 (JP, A) Kaihei 6-183708 (JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) C09C 1/00-3/12 C01G 23/00-23/08 H01B 1/00-1/24 C09D 5/24 C08K 3/00-3/40 C08K 9/02

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 二酸化チタン粒子表面に、アンチモンを
含まずにリンを0.1〜10重量%含む酸化スズの被膜
層を有し、該被膜層を有する二酸化チタン粒子が不活性
ガスで加熱処理されており、且つ230kg/cm2
圧力で加圧成形された成形体が100Ω・cm以下の電
気比抵抗を有することを特徴とする白色導電性二酸化チ
タン粉末。
1. An antimony on the surface of titanium dioxide particles
A coating layer of tin oxide containing 0.1 to 10% by weight of phosphorus and containing no titanium dioxide particles, the titanium dioxide particles having the coating layer are heat-treated with an inert gas, and are applied under a pressure of 230 kg / cm 2. A white conductive titanium dioxide powder, wherein the pressed body has an electrical resistivity of 100 Ω · cm or less.
【請求項2】 請求項1記載の白色導電性二酸化チタン
粉末の製造方法であって、二酸化チタン粒子表面へスズ
の加水反応生成物を均一に沈着させ、その後リンを酸化
スズに対し0.1〜10重量%被膜させ、そして、不活
性ガスで加熱処理することを特徴とする製造方法。
2. The method for producing a white conductive titanium dioxide powder according to claim 1, wherein a reaction product of tin is uniformly deposited on the surface of the titanium dioxide particles, and then phosphorus is added to the tin oxide in an amount of 0.1%. A method for producing a film, wherein the film is coated with 10 to 10% by weight and heat-treated with an inert gas.
【請求項3】 前記不活性ガスでの加熱処理は、非酸化
性雰囲気にて500〜800℃で加熱処理することであ
ることを特徴とする請求項2記載の製造方法。
3. The method according to claim 2, wherein the heat treatment with the inert gas is a heat treatment at 500 to 800 ° C. in a non-oxidizing atmosphere.
【請求項4】 前記不活性ガスでの加熱処理は、不活性
ガスを吹き込みながら行うことであることを特徴とする
請求項3記載の白色導電性二酸化チタン粉末の製造方
法。
4. The method for producing a white conductive titanium dioxide powder according to claim 3, wherein the heat treatment with the inert gas is performed while blowing the inert gas.
JP00335593A 1993-01-12 1993-01-12 White conductive titanium dioxide powder and method for producing the same Expired - Lifetime JP3357107B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP00335593A JP3357107B2 (en) 1993-01-12 1993-01-12 White conductive titanium dioxide powder and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP00335593A JP3357107B2 (en) 1993-01-12 1993-01-12 White conductive titanium dioxide powder and method for producing the same

Publications (2)

Publication Number Publication Date
JPH06207118A JPH06207118A (en) 1994-07-26
JP3357107B2 true JP3357107B2 (en) 2002-12-16

Family

ID=11555046

Family Applications (1)

Application Number Title Priority Date Filing Date
JP00335593A Expired - Lifetime JP3357107B2 (en) 1993-01-12 1993-01-12 White conductive titanium dioxide powder and method for producing the same

Country Status (1)

Country Link
JP (1) JP3357107B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7407606B2 (en) 2003-07-23 2008-08-05 Ishihara Sangyo Kaisha, Ltd. Electroconductive powder and method for production thereof
US7514124B2 (en) 2003-07-23 2009-04-07 Kansai Paint Co., Ltd. White electrically conductive primer composition and method for forming multilayer coating film
WO2011015268A1 (en) 2009-08-03 2011-02-10 Merck Patent Gmbh Conductive powder

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5569412A (en) * 1994-08-18 1996-10-29 E. I. Du Pont De Nemours And Company Tin oxide based conductive powders and coatings
JP2003107778A (en) 2001-09-27 2003-04-09 Fujitsu Ltd Color toner and image forming device using the same
JP4712288B2 (en) * 2003-05-23 2011-06-29 チタン工業株式会社 White conductive powder and its application
JP2005171024A (en) * 2003-12-09 2005-06-30 Kansai Paint Co Ltd White conductive primer coating
KR100931558B1 (en) * 2009-08-28 2009-12-14 에이비씨나노텍 주식회사 Manufacturing process of metallic color pearl pigment by irradiating microwave
JP4956654B2 (en) 2009-09-04 2012-06-20 キヤノン株式会社 Electrophotographic photosensitive member, process cartridge, electrophotographic apparatus, and method of manufacturing electrophotographic photosensitive member
JP4743921B1 (en) 2009-09-04 2011-08-10 キヤノン株式会社 Electrophotographic photosensitive member, process cartridge, and electrophotographic apparatus
WO2012091021A1 (en) * 2010-12-28 2012-07-05 三菱マテリアル株式会社 White conductive powder, conductive mixed powder, dispersion liquid, coating material, and membrane composition
JP5079153B1 (en) * 2011-03-03 2012-11-21 キヤノン株式会社 Electrophotographic photosensitive member, process cartridge and electrophotographic apparatus, and method for manufacturing electrophotographic photosensitive member
JP5054238B1 (en) * 2011-03-03 2012-10-24 キヤノン株式会社 Method for producing electrophotographic photosensitive member
JP5755162B2 (en) * 2011-03-03 2015-07-29 キヤノン株式会社 Method for producing electrophotographic photosensitive member
JP5865182B2 (en) * 2011-06-14 2016-02-17 チタン工業株式会社 Tin oxide-coated conductive powder and method for producing the same
CN102660155B (en) * 2012-05-04 2014-11-05 重庆新华化工有限公司 Titanium dioxide for papermaking
JP5977603B2 (en) * 2012-06-27 2016-08-24 三菱マテリアル電子化成株式会社 White conductive powder, dispersion thereof, paint, and film
JP5977602B2 (en) * 2012-06-27 2016-08-24 三菱マテリアル電子化成株式会社 White conductive powder, dispersion thereof, paint, and film
WO2014003066A1 (en) * 2012-06-27 2014-01-03 三菱マテリアル株式会社 White conductive powder, dispersion liquid thereof, coating material, and film composition
JP6013049B2 (en) * 2012-06-29 2016-10-25 三菱マテリアル電子化成株式会社 White conductive powder, dispersion thereof, paint, film, and method for producing white conductive powder
JP6108842B2 (en) * 2012-06-29 2017-04-05 キヤノン株式会社 Method for producing electrophotographic photosensitive member
JP6061761B2 (en) 2012-08-30 2017-01-18 キヤノン株式会社 Electrophotographic photosensitive member, process cartridge, and electrophotographic apparatus
JP6218502B2 (en) 2012-08-30 2017-10-25 キヤノン株式会社 Electrophotographic photosensitive member, process cartridge, and electrophotographic apparatus

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7407606B2 (en) 2003-07-23 2008-08-05 Ishihara Sangyo Kaisha, Ltd. Electroconductive powder and method for production thereof
US7514124B2 (en) 2003-07-23 2009-04-07 Kansai Paint Co., Ltd. White electrically conductive primer composition and method for forming multilayer coating film
WO2011015268A1 (en) 2009-08-03 2011-02-10 Merck Patent Gmbh Conductive powder

Also Published As

Publication number Publication date
JPH06207118A (en) 1994-07-26

Similar Documents

Publication Publication Date Title
JP3357107B2 (en) White conductive titanium dioxide powder and method for producing the same
JP2959928B2 (en) White conductive resin composition
JP3524550B2 (en) Improved process for producing silica-coated inorganic particles
US5945035A (en) Conductive pigments
JP3444919B2 (en) Conductive pigment
US4373013A (en) Electroconductive powder and process for production thereof
JP2999491B2 (en) Conductive lamellar pigment
US6632276B1 (en) Conductive pigments
JP2959927B2 (en) White conductive powder and method for producing the same
US6096285A (en) Indium tin oxide fine powder and method for preparing the same
US6726856B2 (en) Process for preparing electrically conductive pigments
JP3305405B2 (en) Rod-shaped fine particle conductive titanium oxide and method for producing the same
JPH0782508A (en) Stabilized conductive pigment
JP2994020B2 (en) Method for producing conductive titanium dioxide powder
JPH1111947A (en) Production of antimony doped tin oxide powder and coating material containing the same
DE4237355A1 (en) Electroconductive pigment with shell of fluoride-doped tin oxide - and use in antistatic lacquer, plastics and fibre which is non-toxic and has good properties in use
JP4078660B2 (en) Conductive titanium oxide, process for producing the same, and plastic composition containing the same
JP2858271B2 (en) Method for producing conductive fine powder
JPH0292824A (en) Acicular low oxidized titanium and production thereof
JPH0116776B2 (en)
JP3694901B2 (en) Fluorine-containing metal oxide film and method for producing metal oxide film
JPS61136532A (en) Fibrous white electroconductive substance
JP2731580B2 (en) White conductive potassium hexatitanate fiber and method for producing the same
JPS58209002A (en) Method of producing white conductive powder
JP3226594B2 (en) Method for producing acicular conductive titanium oxide

Legal Events

Date Code Title Description
R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20081004

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20091004

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20101004

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20101004

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111004

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121004

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121004

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20131004

Year of fee payment: 11

EXPY Cancellation because of completion of term
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20131004

Year of fee payment: 11