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JPH02196854A - Conductive resin support for electrophotographic photoreceptors - Google Patents

Conductive resin support for electrophotographic photoreceptors

Info

Publication number
JPH02196854A
JPH02196854A JP1582889A JP1582889A JPH02196854A JP H02196854 A JPH02196854 A JP H02196854A JP 1582889 A JP1582889 A JP 1582889A JP 1582889 A JP1582889 A JP 1582889A JP H02196854 A JPH02196854 A JP H02196854A
Authority
JP
Japan
Prior art keywords
conductive
furnace black
black
weight
resin composition
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
Application number
JP1582889A
Other languages
Japanese (ja)
Other versions
JP2767748B2 (en
Inventor
Toshihiko Tanimoto
谷本 敏彦
Shinji Horie
真司 堀江
Michiya Okamura
岡村 道也
Itsushi Imamura
五士 今村
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.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Petrochemical 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 Mitsubishi Petrochemical Co Ltd filed Critical Mitsubishi Petrochemical Co Ltd
Priority to JP1015828A priority Critical patent/JP2767748B2/en
Publication of JPH02196854A publication Critical patent/JPH02196854A/en
Application granted granted Critical
Publication of JP2767748B2 publication Critical patent/JP2767748B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Conductive Materials (AREA)
  • Photoreceptors In Electrophotography (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To provide a composition having wholly improved mechanical characteristics, processability and appearance while maintaining a high conductivity and suitable for preparing the substrates of electrophotographic sensitive materials by comprising an aromatic polycarbonate, an aromatic polyalkylene terephthalate and a specific carbon black. CONSTITUTION:A conductive resin composition comprises (A) a thermoplastic aromatic polycarbonate in an amount of 60-98wt.% based on the sum of the components A and B, (B) a thermoplastic polyalkylene terephthalate in an amount of 40-2wt.% based on the sum of the component A and B and (C) a carbon black selected from super conductive furnace black (SCF), conductive furnace black (CF), extra conductive furnace black (XCF) and super abrasion furnace black (SAF) in an amount of 3-20 pts.wt. per 100 pts.wt. of the sum of the components A and B.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は導電性樹脂組成物に関し、特に機械的特性、成
形加工性及び外観に優れ、電子写真感光体の導電性支持
体として好適な導電性樹脂組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a conductive resin composition, particularly a conductive resin composition that has excellent mechanical properties, moldability, and appearance, and is suitable as a conductive support for an electrophotographic photoreceptor. The present invention relates to a synthetic resin composition.

[従来の技術J 従来、導電性樹脂は、帯電防止、静電事故防止等、様々
な分野において使用されている。しかしながらこれらの
分野において要求される導電性は低く、高導電性、かつ
、優れた機械的特性、成形加工性が要求される分野にお
いては、未だこれらを満足する導電性樹脂は存在しない
0例えば、電子写真感光体導電支持体において、従来、
金属、例えばアルミニウムを用いていた。
[Prior Art J Conventionally, conductive resins have been used in various fields such as antistatic and electrostatic accident prevention. However, the conductivity required in these fields is low, and in fields where high conductivity, excellent mechanical properties, and moldability are required, there is still no conductive resin that satisfies these requirements.For example, Conventionally, in electrophotographic photoreceptor conductive supports,
Metals such as aluminum were used.

これをプラスチックに代替した場合、高導電性を与える
ことができ、かつ、優れたeaw的特性及び成形加工性
を持つものとして、芳香族ポリカーボネートをベースと
した樹脂組成物が知られている。
When substituted with plastic, a resin composition based on aromatic polycarbonate is known as one that can provide high conductivity and has excellent EW characteristics and moldability.

[発明が解決しようとする課題] しかしながら、芳香族ポリカーボネート樹脂に高導電性
を与えるためには、導電性フィラー、例えばカーボンブ
ラック等を極めて高濃度に配合しなければならず、その
結果、本来芳香族ポリカーボネートが持つ機械的特性、
成形加工性などが著しく低下したり、あるいは、得られ
る製品の外観が極めて悪化し、表面への感光層の接着性
に問題を生じる等の問題があり、特に電子写真感光体導
電支持体への利用は困難であった。
[Problems to be Solved by the Invention] However, in order to impart high conductivity to aromatic polycarbonate resin, conductive fillers such as carbon black must be blended at extremely high concentrations. Mechanical properties of group polycarbonates,
There are problems such as a marked decrease in molding processability, or an extremely poor appearance of the resulting product, and problems with the adhesion of the photosensitive layer to the surface. It was difficult to use.

[課題を解決するための手段] 本発明者らは高導電性樹脂組成物の問題点、即ち高導電
性を保持しつつ機械的特性、成形加工性、製品の外観の
問題等を一挙に解決しようと鋭意研究した結果、芳香族
ポリカーボネートとポリアルキレンテレフタレートの組
合わせに着目し、かつ、特異なカーボンブラックを用い
ることにより、上記課題を解決した。
[Means for Solving the Problems] The present inventors have solved the problems of highly conductive resin compositions, such as mechanical properties, moldability, product appearance, etc., while maintaining high conductivity. As a result of intensive research, we focused on the combination of aromatic polycarbonate and polyalkylene terephthalate and solved the above problem by using a unique carbon black.

即ち、本発明による導電性樹脂組成物は、下肥の(a)
〜(C)からなることを特徴とする熱可塑性樹脂組成物
であって、 (a)を(a)+ (b)基準で60〜98重量%、(
b)を(a)+ (b)基準で40〜2重量%、及び (c)を(a)+ (b) loo重量部に対して3〜
20重量部配置部た導電性樹脂組成物である。
That is, the conductive resin composition according to the present invention can be used for (a)
A thermoplastic resin composition characterized by comprising (C), 60 to 98% by weight of (a) based on (a) + (b), (
b) in an amount of 40 to 2% by weight based on (a) + (b), and (c) in an amount of 3 to 2% by weight based on (a) + (b) loo parts by weight.
This is a conductive resin composition containing 20 parts by weight.

(a)熱可塑性芳香族ポリカーボネート(b)熱可塑性
ポリアルキレンテレフタレート(C)スーパー・コンダ
クティブ・ファーネスブラック(SCF) 、コンタク
チイブ・ファーネスブラック(CF)、エクストラ・コ
ンダクティブ・ファーネスブラック(XCF)及びスー
パー・アブレイジョン・ファーネスブラック(SAF)
から選ばれた少なくとも一種のカーボンブラック L発明の詳細な説明J 青庚底公 本発明により得られる導電性樹脂組成物は。
(a) Thermoplastic aromatic polycarbonate (b) Thermoplastic polyalkylene terephthalate (C) Super conductive furnace black (SCF), contactive furnace black (CF), extra conductive furnace black (XCF) and super conductive furnace black (SCF) Brasion Furnace Black (SAF)
DETAILED DESCRIPTION OF THE INVENTION The conductive resin composition obtained by the present invention includes at least one type of carbon black selected from the following.

種類の熱可塑性樹脂と導電性カーボンブラックとから基
本的に構成される。
It is basically composed of various thermoplastic resins and conductive carbon black.

勉      ポリカーボネート 本発明で使用される二種類の熱可塑性樹脂の一つである
芳香族ポリカーボネートは、炭酸エステルを構成すべき
ジヒドロキシ化合物の少なくとも大部分が二個のフェノ
ール性水酸基を持つものからなるものである。このよう
な二価フェノールとしては、具体的にはビスフェノール
類、特にビスフェノールAがある。
Tsutomu Polycarbonate Aromatic polycarbonate, which is one of the two types of thermoplastic resins used in the present invention, is one in which at least the majority of the dihydroxy compounds that should constitute the carbonate ester have two phenolic hydroxyl groups. be. Specific examples of such dihydric phenols include bisphenols, particularly bisphenol A.

芳香族ポリカーボネートは、上記のような「二価フェノ
ール」をカーボネートプリカーサ−であるホスゲン、ビ
スタロロホーメート、炭酸ジエステル等と反応させるこ
とにより製造されるが、本発明では適当なものを市場で
入手することができる。
Aromatic polycarbonates are produced by reacting the above-mentioned "dihydric phenols" with carbonate precursors such as phosgene, bistaroloformates, carbonic diesters, etc., but in the present invention, suitable polycarbonates can be obtained from commercially available products. can do.

塑 ポリアルキレンテレフタレート 本発明で使用するもう一種類の熱可塑性樹脂であるポリ
アルキレンテレフタレート(FAT)は、アルキレン成
分を構成すべきグリコール成分がエチレングリコール、
トリエチレングリコール、1.4−ブタンジオール、ヘ
キサメチレングリコール、ネオペンチルグリコール、2
.2.4.4−テトラメチレングリコール等の脂肪族の
ジオキシ化合物からなるものが一般に対象となる。これ
らのうちで最も好ましいジオキシ化合物はエチレングリ
コール及びブチレンゲルコールであるが、その40モル
%までを他のジオキシ化合物を用いた混合物も同様に好
ましいものである。
Plastic Polyalkylene Terephthalate Polyalkylene terephthalate (FAT), which is another type of thermoplastic resin used in the present invention, has a glycol component that should constitute an alkylene component such as ethylene glycol,
Triethylene glycol, 1,4-butanediol, hexamethylene glycol, neopentyl glycol, 2
.. 2.4. Those consisting of aliphatic dioxy compounds such as 4-tetramethylene glycol are generally targeted. Among these, the most preferred dioxy compounds are ethylene glycol and butylene gelcol, but mixtures containing up to 40 mol% of other dioxy compounds are also preferred.

一方、このPATのテレフタル酸成分はテレフタル酸の
みからなるものが最も好ましいが、所望によりその40
モル%までを他のジカルボン酸、特に芳香族ジカルボン
酸、例えばイソフタル酸で置き換えてもよい。
On the other hand, the terephthalic acid component of this PAT is most preferably composed only of terephthalic acid, but if desired,
Up to mol % may be replaced by other dicarboxylic acids, especially aromatic dicarboxylic acids, such as isophthalic acid.

本発明で好ましいPATは、ポリエチレンテレフタレー
ト(PET)及びポリブチレンテレフタレート(PBT
)であるが、特に好ましいのはPBTである。PET、
PBTを含めて各種のFATが市場で入手できる。
Preferred PATs in the present invention are polyethylene terephthalate (PET) and polybutylene terephthalate (PBT).
), but PBT is particularly preferred. PET,
Various types of FAT are available on the market, including PBT.

カーポジブラック 本発明で使用するカーボンブラックは、少量の添加量で
組成物に必要な導電性を付与できるものが好ましい、具
体的にはファーネスブラックが不鈍物が少なく、また、
導電性に優れているので好ましいが、その中で、特にフ
ァーネスブラックのX CF IExtracondu
ctive Furnace Black)S CF 
(SuperConductive Furnace 
Black)CF (Conductive Furn
ace BlacklJ5よび5AF(Super A
brasion Furnace Blacklが適用
できる。
Carposi Black The carbon black used in the present invention is preferably one that can impart the necessary conductivity to the composition with a small amount added. Specifically, furnace black has few dull substances, and
Among them, furnace black X CF IExtracondu is preferable because it has excellent conductivity.
active Furnace Black)S CF
(Super Conductive Furnace
Black) CF (Conductive Furn)
ace BlacklJ5 and 5AF (Super A
Brasion Furnace Blackl is applicable.

中でもN2吸着によるBET式比表面積が800 m”
7g以上のものが好ましい、XCFとしてはケッチエン
ブラックインターナショナル社の「ケッチエンブラック
E CJ 、Cabot社の[パルカンxC。
Among them, the BET specific surface area due to N2 adsorption is 800 m”
XCF of 7 g or more is preferable. Examples of XCF include "Ketchen Black E CJ" from Ketsch En Black International, and "Palcan xC" from Cabot.

72]等があり、SCFとしてはCabot社の[パル
カンSCJ、「パルカンP」やDegussa社の「コ
ーラックスL」等があり、CFとしてはCabot社の
「パルカンCJ 、 Co1oua+bian社の「コ
ンダクテックスSCJ等があり、また、SAFとしては
旭カーボン社の「旭#9」、三菱化成工業社の[ダイヤ
ブラックA J 、 Cabot社の「パルカン9」等
がある。これらは併用してもよい、また、これらのカー
ボンブラックが過半量で、かつ、カーボンブラック全体
としてN2吸着によるBET式比表面積が750■”/
g以上、好ましくは800 ts”7g以上、特に90
口■”/g以上であればアセチレンブラック等の他のカ
ーボンブラックを併用してもよい。
72], and SCFs include Cabot's Palcan SCJ and Palcan P, Degussa's Corax L, and CFs include Cabot's Palcan CJ and Co1oua+bian's Conductex SCJ. SAFs include "Asahi #9" by Asahi Carbon Co., Ltd., "Diablack AJ" by Mitsubishi Chemical Industries, Ltd., and "Pulcan 9" by Cabot. These carbon blacks may be used in combination, and if these carbon blacks are the majority, and the carbon black as a whole has a BET specific surface area due to N2 adsorption of 750 ■''/
g or more, preferably 800 ts"7 g or more, especially 90 ts"
Other carbon blacks such as acetylene black may be used in combination as long as the carbon black is 2"/g or more.

住簾剪戒遣 本発明の導電性樹脂組成物には、特に本発明の目的とす
る性質を阻害しない限り、通常樹脂組成物に配合される
各種の付加的成分を含むことができる。このような成分
としては、例えば酸化防止剤、滑剤、離型剤等がある。
The conductive resin composition of the present invention may contain various additional components that are normally incorporated into resin compositions, as long as they do not particularly impede the properties aimed at by the present invention. Examples of such components include antioxidants, lubricants, mold release agents, and the like.

虹成 本発明の導電性樹脂組成物は、上記の各成分は以下の割
合で配合される。
In the conductive resin composition of the present invention, the above-mentioned components are blended in the following proportions.

(a)熱可塑性芳香族ポリカーボネート:(a) + 
(b)基準で60〜98重量%、好ましくは80〜97
重量% (b)熱可塑性PAT : (a) + (b)基準で40〜3重量%、好ましくは
20〜3重量% (clカーボンブラック: 上記1a)÷[bl100重量部に対して3〜20重量
部、好ましくは4〜15重量部 上記の配合において、成分(a)若しくは(b)が上記
範囲を外れた場合、導電率が10”0011以上となり
好ましくない、また、成分(clが上記範囲より少ない
場合には導電率が10”0cm以上となって好ましくな
く、一方、上記範囲より多い場合には成形性及び外観が
悪くなる。
(a) Thermoplastic aromatic polycarbonate: (a) +
(b) 60-98% by weight, preferably 80-97% by weight
Weight% (b) Thermoplastic PAT: 40 to 3% by weight, preferably 20 to 3% by weight based on (a) + (b) (Cl carbon black: 1a above) ÷ [3 to 20% by weight based on 100 parts by weight of bl parts by weight, preferably 4 to 15 parts by weight In the above formulation, if component (a) or (b) is out of the above range, the electrical conductivity will be 10''0011 or more, which is undesirable. When the amount is less, the conductivity becomes 10"0 cm or more, which is not preferable. On the other hand, when it is more than the above range, the moldability and appearance deteriorate.

配立方韮 上記の各成分は、通常の溶融混線法、すなわち−軸押出
機、二軸押出機、ロール、バンバリーなどを適用してベ
レットにすることができる。
The above-mentioned components can be made into pellets by applying a conventional melt mixing method, ie, a screw extruder, a twin screw extruder, a roll extruder, a Banbury, etc.

この混線に際しては、各成分の含有水分については十分
制御する必要がある。各成分の含有水分は、0.5重量
%以下、好ましくは0.2重量%以下、特に11000
pp以下であることが好ましい。
When this crosstalk occurs, it is necessary to sufficiently control the moisture content of each component. The water content of each component is 0.5% by weight or less, preferably 0.2% by weight or less, especially 11000% by weight or less.
It is preferable that it is less than pp.

含有水分量が0.5重量%を超えると製品外観に悪影響
を与えるおそれがある。この水分量は、製造後の組成物
の保管においても注意する必要があり、組成物自体の含
有水分量を0.5重量%以下に抑制することが好ましい
、このため必要に応じて熱風乾燥又は減圧乾燥等の手段
が採用される。
If the water content exceeds 0.5% by weight, it may adversely affect the appearance of the product. It is necessary to pay attention to this water content when storing the composition after production, and it is preferable to suppress the water content of the composition itself to 0.5% by weight or less. For this reason, hot air drying or Measures such as vacuum drying are employed.

[実施例J 以下の実施例及び比較例において、各種の評価測定は次
の方法によった。
[Example J In the following Examples and Comparative Examples, various evaluation measurements were performed by the following methods.

(1)導電性(固有抵抗:0cm) SRIS規格2301−1969ホイーストンブリツジ
法に準拠して測定し、得られた固有抵抗値によって評価
した。
(1) Conductivity (specific resistance: 0 cm) Measured according to SRIS standard 2301-1969 Wheatstone Bridge method, and evaluated based on the obtained specific resistance value.

lOΩ・C■未満をOlそれ以上を×と評価した。Less than 1OΩ·C■ was rated as OI, and more than that was rated as ×.

(2)引張り強さ1kg/閣、21 )、伸び(%)J
IS K−6758に準拠。
(2) Tensile strength 1kg/kaku, 21), elongation (%) J
Compliant with IS K-6758.

引張り強さが6 kg/■−2以上で、かつ、伸びが1
%以上3%未満のものを0、それ以外のものを×と評価
した。
Tensile strength is 6 kg/■-2 or more and elongation is 1
% or more but less than 3% was evaluated as 0, and anything else was evaluated as ×.

(3)成形加工性(MFR:g710分)JIS K−
7210−1975に準拠し、280℃、2.16−k
g荷重におけるVFRを求めた。
(3) Molding processability (MFR: g710 min) JIS K-
7210-1975, 280°C, 2.16-k
The VFR at g load was determined.

0.1 g/10分以上を○、未満を×と評価した。0.1 g/10 minutes or more was evaluated as ○, and less than 0.1 g/10 minutes was evaluated as ×.

(4)外観 Tダイシート成Jf2 mで成形したシートの表面の凹
凸が5μm未満を○、それ以[−を×と評価した。
(4) Appearance T-die sheet formation Jf2m The surface unevenness of the sheet molded with less than 5 μm was evaluated as ◯, and other than that [− was evaluated as ×].

(5)電子写真特性(cm2/mJ) 導電性樹脂シート上に、電69発生剤として、アシッド
ペースト法により処理した無金属フタロシアニンをキャ
スティングを去により厚さ3μmに成膜し、その上に更
に電荷移動剤としてp−ジエチルアミノベンズアルデヒ
ド−(ジフェニルヒドラゾン)を30gm成膜して感光
層を形成せしめて感光体とした。
(5) Electrophotographic characteristics (cm2/mJ) On a conductive resin sheet, metal-free phthalocyanine treated by an acid paste method was formed into a film with a thickness of 3 μm as a charge-69 generating agent, and then further A photoreceptor was prepared by forming a photosensitive layer by depositing 30 g of p-diethylaminobenzaldehyde (diphenylhydrazone) as a charge transfer agent.

得られた感光体をスタブ−インク方式で一6kVの電圧
でコロナ帯電処理し、暗所に1υ秒j1;1保持して初
期表面電位を によって測定したのち、キセノンランプ光をモノクロメ
ータを用いて780nmに分光したrB色光感光体に照
射し、その表面電位が坏に減衰するまでの時1771 
(秒)を求め、露光量(cm′/mJlを算出した。
The obtained photoreceptor was corona charged using a stub-ink method at a voltage of -6 kV, kept in a dark place for 1 υ seconds, and the initial surface potential was measured by xenon lamp light using a monochromator. The rB color photoreceptor is irradiated with 780nm spectroscopy, and the time it takes for its surface potential to decay steadily is 1771.
(seconds), and the exposure amount (cm'/mJl) was calculated.

露光計が100cm2/mJ以−Lのものを05未満の
ものを×と評価した。
Those whose exposure meter measured 100 cm 2 /mJ or more and those whose values were less than 05 were evaluated as ×.

実施例1 メルトフローレー)  (MFR)が4.6g710分
(280℃)のポリカーボネート(三菱瓦斯化学■製ニ
ーピロンE−20fIO) 94.5@遺部、MFRが
4.32r:710分(2圓℃)のポリブヂレンテレフ
タレート(菱化成■製ツバドール5f120) 5.5
 、;TilR部、及び比表面積’J 00 m / 
gのケッチエンブラックEC(ケッチエンブラックイン
ターナショナル社製)111rj+1を部をベント付二
軸押出磯を用いて混i−!12造拉した。
Example 1 Melt flow rate (MFR): 4.6 g 710 minutes (280°C) Polycarbonate (Niepilon E-20fIO manufactured by Mitsubishi Gas Chemical ■) 94.5@Motobe, MFR: 4.32r: 710 minutes (280°C) ℃) polybutylene terephthalate (Tubadol 5F120 manufactured by Ryo Kasei) 5.5
, ;TilR part, and specific surface area 'J 00 m /
Ketchen Black EC (manufactured by Ketchen Black International Co., Ltd.) 111rj+1 of g was mixed using a vented twin-screw extruder. 12 were kidnapped.

i′)られたペレットを゛I゛ダイシート成形機で厚さ
約11のシートを作成し、jIIられなシートの導電性
、引、INり強さ及び伸び、成JFg加T性、外%Mに
一つき評価した。
i') The resulting pellets were made into a sheet with a thickness of about 11 using a die sheet molding machine, and the conductivity, tensile strength, IN tensile strength and elongation, formed JFg, Tability, and external %M of the rolled sheet were evaluated. Rated one for each.

また、得られた導電・hシート上番こ感光層を形成せし
めて11tられた感光体の写α特性を評価した。
In addition, the photographic α characteristics of the photoreceptor obtained by forming a photosensitive layer on the conductive sheet and preparing the photoreceptor were evaluated.

これらの7IlII定値按びに評価を第1表に示す。These 7IlII fixed values and evaluations are shown in Table 1.

比較例1 実施例1において、ポリブヂレンテレフタレートに代え
てポリスチレン(三菱モンサント■製「ダイヤレックス
肝77」)を用いた以外は実施例1と同様にして樹脂組
成物を11な、このものについての各種評価は第1表に
示す。
Comparative Example 1 A resin composition No. 11 was prepared in the same manner as in Example 1 except that polystyrene ("Dialex Kido 77" manufactured by Mitsubishi Monsanto ■) was used in place of polybutylene terephthalate. Various evaluations are shown in Table 1.

比較例2 実施例1において、ウーツチェンブラックECに代えて
比表面積が70m2/gのアセヂレンブラック(−:菱
化成■製3250)を用いた以外は実施例】と同様にし
て樹脂組成物を得た。このものについての−′ト価結果
は第1表に示す。
Comparative Example 2 A resin composition was prepared in the same manner as in Example 1, except that acetylene black (-: 3250 manufactured by Ryo Kasei Corporation) with a specific surface area of 70 m2/g was used in place of Wutzchen black EC. I got it. The -' value results for this product are shown in Table 1.

比較例3 実施例1において、ケッチエンブラックの配合量を25
1f m部として樹脂組成物を得た。このものの評価結
果は第1表に示す。
Comparative Example 3 In Example 1, the blending amount of Ketchen Black was 25%.
A resin composition was obtained as 1f m parts. The evaluation results of this product are shown in Table 1.

第  1 表 [発明の効果] 本発明の導電性熱可塑性樹脂組成物は、導電性カーボン
ブラックと、該導電性カーボンブラックとの親和性が異
なる特定の二l!1類の熱可塑性樹脂を溶融混練するこ
とによって比較的少量の導電性カーボンブラックの配合
によって熱可塑性樹脂に高導電性(体積固有抵抗=10
2Ωcm未満)、優れた機械的特性、かつ、成形加工性
を与えることに成功したものである。このような効果は
、特に電子写11感光体導電支持体として金属アルミニ
ウム等の桟付λとして導電性熱可塑性樹脂を用いること
を可能にするものである。
Table 1 [Effects of the Invention] The conductive thermoplastic resin composition of the present invention has a conductive carbon black and a specific two l! By melting and kneading a Type 1 thermoplastic resin, a relatively small amount of conductive carbon black is blended to give the thermoplastic resin high conductivity (volume resistivity = 10
2 Ωcm), excellent mechanical properties, and moldability. Such an effect makes it possible to use a conductive thermoplastic resin as the crosspiece λ made of metal aluminum or the like, especially as the conductive support for the photoreceptor of the electrophotographic 11.

Claims (1)

【特許請求の範囲】[Claims] (1)下記の(a)〜(c)からなることを特徴とする
熱可塑性樹脂組成物であって、(a)を(a)+(b)
基準で60〜98重量%、(b)を(a)+(b)基準
で40〜2重量%及び(c)を(a)+(b)100重
量部に対して3〜20重量部配合した導電性樹脂組成物
。 (a)熱可塑性芳香族ポリカーボネート (b)熱可塑性ポリアルキレンテレフタレート (c)スーパー・コンダクティブ・ファーネスブラック
(SCF)、コンダクティブ・ファーネスブラック(C
F)、エクストラ・コンダクティブ・ファーネスブラッ
ク(XCF)及びスーパー・アプレイジョン・ファーネ
スブラック(SAF)から選ばれた少なくとも一種のカ
ーボンブラック
(1) A thermoplastic resin composition characterized by consisting of the following (a) to (c), in which (a) is replaced by (a) + (b).
60 to 98 weight % based on the standard, 40 to 2 weight % based on (a) + (b) of (b), and 3 to 20 parts by weight of (c) based on 100 parts by weight of (a) + (b). conductive resin composition. (a) Thermoplastic aromatic polycarbonate (b) Thermoplastic polyalkylene terephthalate (c) Super conductive furnace black (SCF), conductive furnace black (C
F) at least one carbon black selected from Extra Conductive Furnace Black (XCF) and Super Appreciation Furnace Black (SAF)
JP1015828A 1989-01-24 1989-01-24 Conductive resin support for electrophotographic photoreceptor Expired - Lifetime JP2767748B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1015828A JP2767748B2 (en) 1989-01-24 1989-01-24 Conductive resin support for electrophotographic photoreceptor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1015828A JP2767748B2 (en) 1989-01-24 1989-01-24 Conductive resin support for electrophotographic photoreceptor

Publications (2)

Publication Number Publication Date
JPH02196854A true JPH02196854A (en) 1990-08-03
JP2767748B2 JP2767748B2 (en) 1998-06-18

Family

ID=11899710

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP2767748B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4208644A1 (en) * 1992-03-18 1993-09-23 Bayer Ag ANTISTATIC POLYCARBONATE EXTRUSION FILMS
US8999200B2 (en) 2002-07-23 2015-04-07 Sabic Global Technologies B.V. Conductive thermoplastic composites and methods of making

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60115665A (en) * 1983-11-25 1985-06-22 Kyowa Yuka Kk Method for reforming carbon black
JPS62185743A (en) * 1986-02-12 1987-08-14 Teijin Chem Ltd Resin composition

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60115665A (en) * 1983-11-25 1985-06-22 Kyowa Yuka Kk Method for reforming carbon black
JPS62185743A (en) * 1986-02-12 1987-08-14 Teijin Chem Ltd Resin composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4208644A1 (en) * 1992-03-18 1993-09-23 Bayer Ag ANTISTATIC POLYCARBONATE EXTRUSION FILMS
JPH0641414A (en) * 1992-03-18 1994-02-15 Bayer Ag Antistatic extruded polycarbonate sheet
US5360658A (en) * 1992-03-18 1994-11-01 Bayer Aktiengesellschaft Antistatic extruded polycarbonate sheets
US8999200B2 (en) 2002-07-23 2015-04-07 Sabic Global Technologies B.V. Conductive thermoplastic composites and methods of making

Also Published As

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