JPS60115665A - Method for reforming carbon black - Google Patents

Method for reforming carbon black

Info

Publication number
JPS60115665A
JPS60115665A JP58221862A JP22186283A JPS60115665A JP S60115665 A JPS60115665 A JP S60115665A JP 58221862 A JP58221862 A JP 58221862A JP 22186283 A JP22186283 A JP 22186283A JP S60115665 A JPS60115665 A JP S60115665A
Authority
JP
Japan
Prior art keywords
carbon black
acid
treated
compd
heat
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
Application number
JP58221862A
Other languages
Japanese (ja)
Inventor
Kiyoshi Fujita
潔 藤田
Reikichi Nozawa
野沢 玲吉
Tokuyuki Yoshimoto
特行 吉元
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.)
KH Neochem Co Ltd
Original Assignee
Kyowa Yuka 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 Kyowa Yuka Co Ltd filed Critical Kyowa Yuka Co Ltd
Priority to JP58221862A priority Critical patent/JPS60115665A/en
Publication of JPS60115665A publication Critical patent/JPS60115665A/en
Pending legal-status Critical Current

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  • Carbon And Carbon Compounds (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)

Abstract

PURPOSE:To reform carbon black to have excellent properties as an electrically conductive material, by heat-treating carbon black in the presence of a specified compd. in an inert atmosphere. CONSTITUTION:Carbon black (pref. one having a large surface area, pref. 800m<2>/ g or above, DBP absorption of 250ml/100g or above and high electrical conductivity) is heat-treated at 250-800 deg.C in the presence of a higher fatty acid (e.g. palmitic or oleic acid), a base (e.g. lutidine), an arom. compd. (e.g. t-stilbene), an ester (e.g. tristearin), a sulfur compd. (e.g. dephenyl disulfide) or a polyol (e.g. polyglycerol) and air-cooled, thus obtaining reformed carbon black having excellent properties as an electrically conductive material. It is desirable that when raw carbon black contains a large quantity of metal, it is treated with a mineral acid to remove the metal.

Description

【発明の詳細な説明】 本発明は、カーボンブラック(以下、CBともいう)の
改質方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for modifying carbon black (hereinafter also referred to as CB).

CBは最近、高圧ケーブル、面発熱体1通信ケーブル、
&i気テープ、ビデオディスク、@&i波遮へい材料、
静電防止材料、導電塗料、ゼログラフィー用トナー等、
有機導電材料用途として開発されつつある。
CB has recently been developing high voltage cables, surface heating element 1 communication cables,
& i-wave tape, video disc, @ & i-wave shielding material,
Antistatic materials, conductive paints, toner for xerography, etc.
It is being developed as an organic conductive material.

これらの新材料の開発に際し“ζはCBそのものは言う
に及ばず、CBと混合するポリマー、モノマー、その他
の化合物との物押的化学的メカニズムを最適に制御、設
計して特性を付与することは重要なR題となっている。
When developing these new materials, ``ζ'' is not only about CB itself, but also about the optimal control and design of physical chemical mechanisms between CB and the polymers, monomers, and other compounds that are mixed with it to impart properties. has become an important R topic.

上記用途として用いられるCBは高導電性のCBである
ことが好ましく、例えばアセチレン・ブランク、コンダ
クティブ・ファーネス・ブランク、チャンネル・ブラッ
ク、部分酸化法ガスプロセス副生カーボン・ブラック等
が例示される。
The CB used for the above purpose is preferably a highly conductive CB, such as an acetylene blank, a conductive furnace blank, a channel black, a by-product carbon black from a partial oxidation gas process, and the like.

アセチレン・ブランクはサーマル法あるいはファーネス
法によって高純度のアセチレンガスから得られる。コン
ダクティブ・ファーネス・ブラックはファーネス法によ
って得られる高表面積、高吸油量(DBP)のブランク
で、特に−次粒子径が比較的小さく、多孔性又はエラグ
シェル型粒子を多く含み、それらの粒子を数十〜数百融
着し゛(ストラフチュー構造を発達させた場合に樹脂中
でも高導電性を発現する。チャンネル・シラツクはチャ
ンネル法によって得られるCBである。副生CBは油性
原料から部分燃焼で水生ガスなどを発生させた際得られ
るCBである。
Acetylene blanks are obtained from high purity acetylene gas by thermal or furnace methods. Conductive Furnace Black is a blank with high surface area and high oil absorption (DBP) obtained by the furnace method, which has a relatively small secondary particle size and contains many porous or elastomer-type particles. ~Hundreds of fused ゛ (high conductivity is exhibited even in resin when a strafute structure is developed.Channel Silk is CB obtained by the channel method.By-product CB is partially burned from oily raw materials such as aquatic gas etc. This is the CB obtained when generating .

これらCBは小量の水素と酸素を含有し、それらけ官能
基としてCBの表面もしくは表面近くに存在する。例え
ばフェノール(> OH1弱酸性)キノン(>−〇)カ
ルボン酸く〉COす11、強酸性)、ラクトン(>C0
0−) 、活性水素(> −II )等である。これら
は一般に電子をトラップし、導電性を減少させる方向に
作用し、樹脂との混合、成型に際し親和性に影響を与え
ると考えられる。
These CBs contain small amounts of hydrogen and oxygen, which are present as functional groups on or near the surface of the CB. For example, phenol (>OH1, weakly acidic), quinone (>-0) carboxylic acid, COS11, strongly acidic), lactone (>C0
0-), active hydrogen (>-II), and the like. These generally trap electrons and act to reduce conductivity, and are thought to affect the affinity when mixed with resin and molded.

樹脂特にPVCを高ストラクチュアーのCBと混練する
に際しては自己発熱し、PVCの熱分解を促し、成型品
の品質劣化をもたらす。
When resin, especially PVC, is kneaded with highly structured CB, self-heating occurs, which promotes thermal decomposition of PVC, resulting in quality deterioration of molded products.

またCBの種類によっては品質調整のために微量の金属
塩などが加えられ、あるいは製造工程においてこれらが
混入してくる。これらは時として材料に好ましくない影
響をあたえる。この金属の除去は酸処理によってできる
が、CBのp Hの低下を招き、例えばPVCと混練す
るとPVCの安定性が低下する。
Also, depending on the type of CB, trace amounts of metal salts may be added for quality control, or these may be mixed in during the manufacturing process. These sometimes have undesirable effects on the material. This metal can be removed by acid treatment, but this results in a decrease in the pH of CB, and when it is kneaded with PVC, for example, the stability of PVC decreases.

導電材料として優れた性質を有するCBの製法について
検討の結果、高級脂肪酸、塩基、芳香族系化合物、エス
テル、いおう含有化合物またはポリオールの存在下に不
活性ガス雰囲気下においてCBを250〜800℃、好
ましくは300〜400℃で1〜10時間加熱処理する
ことによって導電材料として優れたCBが得られること
が見出された。
As a result of studies on the manufacturing method of CB, which has excellent properties as a conductive material, CB was heated at 250 to 800°C in the presence of higher fatty acids, bases, aromatic compounds, esters, sulfur-containing compounds, or polyols under an inert gas atmosphere. It has been found that CB excellent as a conductive material can be obtained by heat treatment preferably at 300 to 400°C for 1 to 10 hours.

原料として用いられるCBはいずれのものも用いられる
が、例えば前述のCBが用いられる。特に表面積が大き
く、好ましくは800 rrl/g以上DBP吸収i!
250ml/ 100 g以上の導電性の高いCBが好
ましく用いられる。
Although any CB can be used as a raw material, for example, the above-mentioned CB is used. In particular, the surface area is large, preferably 800 rrl/g or more DBP absorption i!
CB with high conductivity of 250 ml/100 g or more is preferably used.

CBが金属を多量に含有する場合は熱処理に先立ってC
Bを鉱酸例えば塩酸、硫酸等で処理し゛ζ脱金属を行う
。又は、先に熱処理を行ったのち、鉱酸で脱金属を行う
。この処理は通常1〜lO%の濃度で1〜10時間必要
に応じて200℃以下の温度で処理される。処理後水洗
を行い、必要に応じアンモニア水等で中和、水洗される
If CB contains a large amount of metal, C
B is treated with a mineral acid such as hydrochloric acid or sulfuric acid to perform ζ-demetallization. Alternatively, after heat treatment is performed first, demetallization is performed using a mineral acid. This treatment is usually carried out at a concentration of 1 to 10% for 1 to 10 hours, if necessary, at a temperature of 200° C. or lower. After treatment, it is washed with water, and if necessary, it is neutralized with aqueous ammonia and washed with water.

高級脂肪酸としては炭素数7〜23の脂肪酸、例えばバ
ルミチン酸、ラウリン酸、イソステアリン酸、1.2−
ヒドロキシステアリン酸、ヘヘン酸。
Examples of higher fatty acids include fatty acids having 7 to 23 carbon atoms, such as valmitic acid, lauric acid, isostearic acid, 1.2-
Hydroxystearic acid, hehenic acid.

カプリル酸等の飽和脂肪酸、オレイン酸等の不飽和脂肪
酸が用いられる。
Saturated fatty acids such as caprylic acid and unsaturated fatty acids such as oleic acid are used.

塩基としては2.3ベンゾピリジン、ルチジン、ステア
リルアミン、インドール、ヘキサメチレンジアミン、ト
リエタノールアミン、1.3ジフエニルグアニジン、ア
ンモニア、アンモニアとステアリン酸、εカプロラクタ
ム、メラミン、ジフェニルチオ尿素、グルタミン酸等が
あげられ、芳香族系化合物としてはt−スチルベン、α
−フェニルケイ皮酸、ケイ皮酸メチル、スチレン、ビフ
ェニル、アントラセン、ビスヒエノールA等があげられ
、エステルとしてはトリメリット酸トリアリル、グリャ
ロールモノスチアレート、トリステアリン、PEGモノ
ステアレート、リシノール酸ステアリル、マレイン酸モ
ノメチル等があげられ、いおう含有化合物としてはチオ
ジグリコール酸オクタデシル、ジフェニルジスルフィド
、ベンゾチオフェン、2−ナフタリンチオール、2メル
カプトベンゾチアゾール、4.4’ジチオモルホリン、
テトラメチルチウラムジスルフィド等があげられ、ポリ
オールとしては、ポリグリセリン、1.6ヘキサンジオ
ール等があげられる。
Examples of bases include 2.3 benzopyridine, lutidine, stearylamine, indole, hexamethylenediamine, triethanolamine, 1.3 diphenylguanidine, ammonia, ammonia and stearic acid, ε-caprolactam, melamine, diphenylthiourea, glutamic acid, etc. Examples of aromatic compounds include t-stilbene, α
- Phenylcinnamic acid, methyl cinnamate, styrene, biphenyl, anthracene, bishyenol A, etc., and the esters include triallyl trimellitate, glyarol monostearate, tristearin, PEG monostearate, stearyl ricinoleate. , monomethyl maleate, etc., and sulfur-containing compounds include octadecyl thiodiglycolate, diphenyl disulfide, benzothiophene, 2-naphthalethiol, 2-mercaptobenzothiazole, 4.4' dithiomorpholine,
Examples of the polyol include tetramethylthiuram disulfide and the like, and examples of the polyol include polyglycerin and 1.6 hexanediol.

これらはCBの1〜lO%用いられる。These are used in an amount of 1 to 10% of CB.

CBと上記添加化合物は通常熱処理に先立ってよく混合
してから熱処理される。必要に応じて溶媒を混合に際し
て用いることがてきる処理装置は例えばロータリーキル
ンが用いうる。
CB and the above-mentioned additive compound are usually mixed well prior to heat treatment and then heat treated. A rotary kiln, for example, can be used as a processing device that can use a solvent during mixing if necessary.

加熱処理後自然冷却によって目的物を得る。After heat treatment, the desired product is obtained by natural cooling.

本発明方法によって優れた性質を有する改質CBが得ら
れる。その作用機構については明らかではないが、CB
裏表面は前述の如く官能基が存在し、本発明の処理によ
って一部脱炭酸して分解し、一部エステル化してpHを
向上せしめ、CBの表向の活性点を減少せしめて樹脂に
対する親和力を増加せしめるものと推定され、特に樹脂
との混合成葺1.−)−12’lム柄ス道饋1矛會りの
珈面江酊) t、−117,岡2小を与えるものと推定
される。
Modified CB with excellent properties can be obtained by the method of the present invention. Although its mechanism of action is not clear, CB
As mentioned above, the back surface has functional groups, which are partially decarboxylated and decomposed by the treatment of the present invention, and partially esterified to improve the pH, reduce the active sites on the surface of CB, and increase the affinity for the resin. It is estimated that this will increase -) -12'l Musu way 1 conflict meeting's coffee face drunkenness) It is estimated that it gives t, -117, Oka 2 grade.

本発明の態様を実施例によって説明する。Aspects of the present invention will be illustrated by examples.

実施例1゜ 10(lガラスフラスコに5%塩酸60k[を入れ、こ
れに第1表に示すカーボンブラック(ブラックパール2
000 Cabot社製)を3 kg入れて、95℃で
6hrおだやかに攪拌する。冷却後濾過、水洗を濾液中
の塩素イオン濃度がIOppm以下になるまでくりかえ
し、5%アンモニア水を加えてpHを10にする。濾過
、水洗を塩素イオンがlppm以下になるまでくりかえ
し、得られる濾滓を真空乾燥して脱金属処理カーボンブ
ランクを得る。得られたカーボンブラックの物性を第1
表に示す。
Example 1 60k of 5% hydrochloric acid was placed in a 10 l glass flask, and carbon black (Black Pearl 2) shown in Table 1 was added to it.
000 (manufactured by Cabot) and stirred gently at 95°C for 6 hours. After cooling, filtration and washing with water are repeated until the chloride ion concentration in the filtrate is below IOppm, and the pH is adjusted to 10 by adding 5% aqueous ammonia. The filtration and water washing are repeated until the chlorine ions are reduced to 1 ppm or less, and the resulting filter cake is vacuum dried to obtain a demetallized carbon blank. The physical properties of the obtained carbon black are
Shown in the table.

第 1 表 第 3 表 * この例は、鉱酸処理、水洗、中和、水洗後のCBス
ラリーに2,3−ベンゾピリジンを溶解し、混合後、濾
過、真空乾燥したCBを新たに添加剤を加えることなく
熱処理した。
Table 1 Table 3 * In this example, 2,3-benzopyridine is dissolved in the CB slurry after mineral acid treatment, water washing, neutralization, and water washing, and after mixing, filtered and vacuum-dried CB is added as a new additive. Heat treated without adding.

実施例4゜ 実施例3において、2.3ベンゾピリジンの代わりに第
4表に示す添加剤を用いる以外は実施例3と同様にして
第4表の結果を得た。
Example 4 The results shown in Table 4 were obtained in the same manner as in Example 3, except that the additives shown in Table 4 were used instead of 2.3 benzopyridine.

第 4 表 添 加 剤 処理 体積固を 温度 pH全酸量 抵 抗 熱安定性 (%) ℃) (ΩcIl) ルチンy 330 B、7 69 10.6 12.0
/194ステアリル 330 9.4 41 11.1
 9.0/194アミン インドール 330 8.7 71 10.4 10.
5/191ヘキ’tfiチレ330 8.7 59 1
1.0 9.5/190ンジアミン トリエタノ−3308,16610,014,0/19
3ルアミン 1.3ジフエニ 350 8.9 53 12.6 1
0.0/191ルグアニジン 7ンモニ7” 330 9.3 39 8.5 11.
0/194アンモニア+ 350 9.7 48 8.
5 15.0/192導父アリン酸 −ブロラク 330 8.7 51 B、9 13.0
/192・7ム Jラミ:i 330 B、5 61 B、4 10.5
/193symジフェニ 330 8.7 55 B、
7 11.0/193ルチオ尿素 *アンモニアは、CB200gを充填したロータリーキ
ルンに2.3 N 12 / h供給した。
Table 4 Additive Treatment Volume solidity Temperature pH Total acid amount Resistance Thermal stability (%) °C) (ΩcIl) Rutin y 330 B, 7 69 10.6 12.0
/194 Stearyl 330 9.4 41 11.1
9.0/194 Amine Indole 330 8.7 71 10.4 10.
5/191 Heki'tfi Chile 330 8.7 59 1
1.0 9.5/190 Diamine Triethano-3308,16610,014,0/19
3 amine 1.3 diphenylene 350 8.9 53 12.6 1
0.0/191 Luguanidine 7” 330 9.3 39 8.5 11.
0/194 ammonia + 350 9.7 48 8.
5 15.0/192 Guider arylic acid-brolac 330 8.7 51 B, 9 13.0
/192.7 Mu J Rami: i 330 B, 5 61 B, 4 10.5
/193sym Dipheni 330 8.7 55 B,
7 11.0/193 ruthiourea*Ammonia was supplied at 2.3 N 12 /h to a rotary kiln filled with 200 g of CB.

**ステアリン酸を5%混合した上で、アンモニアの場
合と同じ方法で処理した。
** 5% stearic acid was mixed and treated in the same manner as ammonia.

Claims (1)

【特許請求の範囲】 1 高級脂肪酸、塩基、芳香族系化合物、エステル、い
おう含有化合物又はポリオールの存在下にカーボンブラ
ンクを不活性ガス雰囲気下、250−800℃の温度で
加熱処理することを特徴とするカーボンブラックの改質
方法。 2 該処理に先立ってカーボンブラックが鉱酸で処理さ
れる特許請求の範囲第1項記載の方法。 3 該処理のあとにカーボンブランクが鉱酸で処理され
る特許請求の範囲第1項記載の方法。
[Claims] 1. A carbon blank is heat-treated at a temperature of 250 to 800°C in an inert gas atmosphere in the presence of a higher fatty acid, a base, an aromatic compound, an ester, a sulfur-containing compound, or a polyol. A method for modifying carbon black. 2. The method of claim 1, wherein the carbon black is treated with a mineral acid prior to said treatment. 3. A method according to claim 1, wherein after said treatment the carbon blank is treated with a mineral acid.
JP58221862A 1983-11-25 1983-11-25 Method for reforming carbon black Pending JPS60115665A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58221862A JPS60115665A (en) 1983-11-25 1983-11-25 Method for reforming carbon black

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58221862A JPS60115665A (en) 1983-11-25 1983-11-25 Method for reforming carbon black

Publications (1)

Publication Number Publication Date
JPS60115665A true JPS60115665A (en) 1985-06-22

Family

ID=16773349

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58221862A Pending JPS60115665A (en) 1983-11-25 1983-11-25 Method for reforming carbon black

Country Status (1)

Country Link
JP (1) JPS60115665A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02196854A (en) * 1989-01-24 1990-08-03 Mitsubishi Petrochem Co Ltd Conductive resin composition
KR19980060803A (en) * 1996-12-31 1998-10-07 손욱 Method for producing a conductive agent and a secondary battery containing the conductive agent
KR20020061951A (en) * 2001-01-19 2002-07-25 주식회사 솔나노켐 Methods for Modifying Interfacial Properties of Fillers
EP0799281B2 (en) 1994-12-15 2006-03-29 Cabot Corporation Carbon black reacted with diazonium salts and products
JP2006518797A (en) * 2003-02-21 2006-08-17 ダウ グローバル テクノロジーズ インコーポレイティド Moisture crosslinkable polymeric composition

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02196854A (en) * 1989-01-24 1990-08-03 Mitsubishi Petrochem Co Ltd Conductive resin composition
EP0799281B2 (en) 1994-12-15 2006-03-29 Cabot Corporation Carbon black reacted with diazonium salts and products
KR19980060803A (en) * 1996-12-31 1998-10-07 손욱 Method for producing a conductive agent and a secondary battery containing the conductive agent
KR20020061951A (en) * 2001-01-19 2002-07-25 주식회사 솔나노켐 Methods for Modifying Interfacial Properties of Fillers
JP2006518797A (en) * 2003-02-21 2006-08-17 ダウ グローバル テクノロジーズ インコーポレイティド Moisture crosslinkable polymeric composition

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