JPH0676511B2 - Conductive resin composition - Google Patents
Conductive resin compositionInfo
- Publication number
- JPH0676511B2 JPH0676511B2 JP28039484A JP28039484A JPH0676511B2 JP H0676511 B2 JPH0676511 B2 JP H0676511B2 JP 28039484 A JP28039484 A JP 28039484A JP 28039484 A JP28039484 A JP 28039484A JP H0676511 B2 JPH0676511 B2 JP H0676511B2
- Authority
- JP
- Japan
- Prior art keywords
- resin composition
- carbon
- conductive resin
- resistance
- temperature
- 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
Links
- 239000011342 resin composition Substances 0.000 title claims description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 22
- 239000011230 binding agent Substances 0.000 claims description 5
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 description 15
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000002667 nucleating agent Substances 0.000 description 6
- 229920000620 organic polymer Polymers 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- 239000005711 Benzoic acid Substances 0.000 description 3
- 235000010233 benzoic acid Nutrition 0.000 description 3
- FMZUHGYZWYNSOA-VVBFYGJXSA-N (1r)-1-[(4r,4ar,8as)-2,6-diphenyl-4,4a,8,8a-tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol Chemical compound C([C@@H]1OC(O[C@@H]([C@@H]1O1)[C@H](O)CO)C=2C=CC=CC=2)OC1C1=CC=CC=C1 FMZUHGYZWYNSOA-VVBFYGJXSA-N 0.000 description 2
- 229920006038 crystalline resin Polymers 0.000 description 2
- 229940087101 dibenzylidene sorbitol Drugs 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical compound [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 2
- UOBYKYZJUGYBDK-UHFFFAOYSA-N 2-naphthoic acid Chemical compound C1=CC=CC2=CC(C(=O)O)=CC=C21 UOBYKYZJUGYBDK-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- CSJKPFQJIDMSGF-UHFFFAOYSA-K aluminum;tribenzoate Chemical compound [Al+3].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 CSJKPFQJIDMSGF-UHFFFAOYSA-K 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 235000010237 calcium benzoate Nutrition 0.000 description 1
- 239000004301 calcium benzoate Substances 0.000 description 1
- HZQXCUSDXIKLGS-UHFFFAOYSA-L calcium;dibenzoate;trihydrate Chemical compound O.O.O.[Ca+2].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 HZQXCUSDXIKLGS-UHFFFAOYSA-L 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000002491 polymer binding agent Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 235000010235 potassium benzoate Nutrition 0.000 description 1
- 239000004300 potassium benzoate Substances 0.000 description 1
- 229940103091 potassium benzoate Drugs 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- XTIVBOWLUYDHKE-UHFFFAOYSA-M sodium;cyclohexanecarboxylate Chemical compound [Na+].[O-]C(=O)C1CCCCC1 XTIVBOWLUYDHKE-UHFFFAOYSA-M 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】 産業上の利用分野 本発明は長時間に渡って抵抗が安定で発熱温度が均一な
正温度係数を有するカーボン系の導電性樹脂組成物に関
するものである。TECHNICAL FIELD The present invention relates to a carbon-based conductive resin composition having a positive temperature coefficient in which resistance is stable for a long time and heat generation temperature is uniform.
従来の技術 従来のこの種の正温度係数を有するカーボン系導電性樹
脂組成物の多くは、結晶性を有する有機高分子結合体に
カーボン粉末を混入しカーボンストラクチュアーの接
触,カーボン単味の接触等によって導電性を得ている。
そして温度の制御はその結晶性有機高分子結合体の膨張
あるいは収縮等の変化,球晶変化等によってカーボン接
触点の切り離し、接触等が適宜行なわれることによって
抵抗変化が自動的に行なわれ、一定の温度を示す仕組み
になっている。2. Description of the Related Art Most of the conventional carbon-based conductive resin compositions having this type of positive temperature coefficient are formed by mixing carbon powder into an organic polymer binder having crystallinity to make contact with a carbon structure or a simple contact with carbon. And so on.
The temperature is controlled by changing the expansion or contraction of the crystalline organic polymer conjugate, separating the carbon contact point by changing the spherulite, and performing the contact appropriately to automatically change the resistance. It is a mechanism that indicates the temperature of.
発明が解決しようとする問題点 しかし、この種の正温度係数を有する導電性樹脂組成物
は、結晶性有機高分子を主にしているため、使用温度、
経過時間等によって結晶性有機高分子の球晶が成長しカ
ーボン接触点が少なくなると共に電流のパス距離が長く
なり、抵抗の増加現象が現われるのである。このことに
よって導電性樹脂組成物の温度が上昇し抵抗体として危
険にさらされるのである。そこで、本発明はこのような
カーボン系の正温度係数を有する導電性樹脂組成物にお
いて長期間の使用でも抵抗の変化が少なく、安定した温
度特性を有する導電性樹脂組成物を得ようとするもので
ある。Problems to be Solved by the Invention However, since the conductive resin composition having a positive temperature coefficient of this kind is mainly composed of a crystalline organic polymer, the operating temperature,
The spherulite of the crystalline organic polymer grows with the passage of time, the number of carbon contact points decreases, the current path length increases, and the phenomenon of increased resistance appears. As a result, the temperature of the conductive resin composition rises and it is endangered as a resistor. Therefore, the present invention intends to obtain a conductive resin composition having such a carbon-based positive temperature coefficient that resistance changes little even after long-term use and has stable temperature characteristics. Is.
問題点を解決するための手段 そこで、これらの問題点を解決する本発明の技術的な手
段は、結晶性を有する有機結合材とカーボン粉末及び構
造式が (但し、RはH,CH3,C2H5、MはAl,Na,K,Ca)で示される
化合物を0.1wt%以上5wt%未満添加して成り、前記結晶
性を有する有機結合材の球晶を微細化する前記構造式で
示した核剤物質を添加し、通常の使用状態において球晶
の成長を抑制しカーボン接触点の変化を少なくし抵抗の
安定化をはかり、長期の使用状態においても安定な一定
した温度を有する組成物を得るものである。Therefore, the technical means of the present invention for solving these problems is that an organic binder having crystallinity, carbon powder, and a structural formula are used. (However, R is H, CH 3 , C 2 H 5 , and M is Al, Na, K, Ca) 0.1 wt% or more and less than 5 wt% is added, and the organic binder having the crystallinity is formed. The nucleating agent shown in the above structural formula for refining the spherulites is added to suppress the growth of spherulites under normal use conditions, reduce the change in carbon contact points, and stabilize the resistance to ensure long-term use. It is intended to obtain a composition having a stable and constant temperature even in a state.
作 用 この技術的手段による作用は次のようになる。すなわ
ち、結晶性有機高分子を用いたカーボン系導電性樹脂組
成物において、使用状態、時間経過等により、該結晶性
有機高分子の球晶が成長しカーボン接触点の一部切り離
しによる電流パス距離が長くなり抵抗の増加及び温度の
上昇を来たすのである。この様な現象をなくすために球
晶の拡大化を抑制し、均一微細化作用のある核剤物質を
添加しカーボン接触点の切り離しによる抵抗の変化、温
度の変化を抑制することにある。このことによりカーボ
ン接触点の変化が少なくなると共に一定した抵抗値を示
し、長期間に渡って安定な正温度係数を示すカーボン系
導電性樹脂組成物が得られるのである。Operation The effects of this technical means are as follows. That is, in a carbon-based conductive resin composition using a crystalline organic polymer, a spherulite of the crystalline organic polymer grows due to use conditions, time passage, etc., and a current path distance due to partial separation of carbon contact points. Becomes longer, resulting in an increase in resistance and a rise in temperature. In order to eliminate such a phenomenon, expansion of spherulites is suppressed, and a nucleating agent substance having a uniform refining effect is added to suppress change in resistance and change in temperature due to separation of carbon contact points. As a result, it is possible to obtain a carbon-based conductive resin composition which has a small change in carbon contact point, a constant resistance value, and a stable positive temperature coefficient over a long period of time.
実施例 以下、本発明の実施例を図により説明する。Example Hereinafter, an example of the present invention will be described with reference to the drawings.
〔実施例1〜5〕 カーボン粉末にビニルシラン0.5%溶液を添加し、撹拌
熟成の後、ビニルシラン処理カーボン粉末を得た。[Examples 1 to 5] A vinylsilane 0.5% solution was added to carbon powder, and after aging with stirring, vinylsilane-treated carbon powder was obtained.
このカーボン粉末に第1の有機結合材として有機酸変性
したポリエチレンと核剤として安息香酸(C6H5COOH)を
表の組成に従って150〜180℃、75rpm10〜15分間混練し
カーボンを含む樹脂組成物を得た。A resin composition containing carbon by kneading this carbon powder with polyethylene modified with an organic acid as a first organic binder and benzoic acid (C 6 H 5 COOH) as a nucleating agent according to the composition in the table at 150 to 180 ° C. and 75 rpm for 10 to 15 minutes. I got a thing.
この組成物を粉砕の後、第2の有機結合材としてオレフ
イン系エラストマーを添加し、最終カーボンの含有量が
30wt%になる様調整した。このようにして得た導電性樹
脂組成物に銅電極を形成しアニール後、抵抗〜時間の性
能を評価した。この結果を図に示す。After crushing this composition, an olefin elastomer is added as a second organic binder, and the final carbon content is
Adjusted to be 30wt%. A copper electrode was formed on the conductive resin composition thus obtained, and after annealing, the performance of resistance to time was evaluated. The results are shown in the figure.
〔実施例6〜10〕 実施例1〜5と同様に核剤作用として示す。ジベンジリ
デンソルビトール(ゲルオールMD;新日本理化製)C22H
26O6を安息香酸の代わりに加え図に示す同様の結果を得
た。 [Examples 6 to 10] Similar to Examples 1 to 5, the action is shown as a nucleating agent. Dibenzylidene sorbitol (Gel-ol MD; Shin Nippon Rika) C 22 H
26 O 6 was added instead of benzoic acid and similar results as shown in the figure were obtained.
なお本願において核剤として安息香酸及びジベンジリデ
ンソルビトールを用いたが、安息香酸アルミニウム、安
息香酸カリウム、安息香酸カルシウム、安息香酸ナトリ
ウム、β−ナフトエ酸ナトリウム、シクロヘキサンカル
ボン酸ナトリウム、等いづれを用いても本発明と同様の
効果が得られることを確認している。又、本実施例にお
いて核剤を添加して最も効果が得られるのは0.3wt%で
あったが5wt%未満であれば充分な効果が得られた。し
かし、5wt%以上添加するとコスト的にも高くなり経済
的に効果が得られるものではなかった。Although benzoic acid and dibenzylidene sorbitol were used as nucleating agents in the present application, aluminum benzoate, potassium benzoate, calcium benzoate, sodium benzoate, sodium β-naphthoate, sodium cyclohexanecarboxylate, etc. may be used. It has been confirmed that the same effect as the present invention can be obtained. Further, in the present example, the maximum effect was obtained by adding the nucleating agent to 0.3 wt%, but if it was less than 5 wt%, a sufficient effect was obtained. However, if it is added in an amount of 5 wt% or more, the cost becomes high and the economical effect cannot be obtained.
発明の効果 以上、本発明によると、結晶性樹脂を含む導電性組成物
において、結晶性樹脂の球晶は経年及び、温度等の使用
状況により成長拡大し導電物質の接触点を切り難し抵抗
の増大現象がある。しかし、本願のように球晶を微細均
一化する物質を添加し、微細均一化することによりその
成長がなくなりカーボン接触点の切り離しがなくなり抵
抗の長期に渡って均一化がはかれるのである。As described above, according to the present invention, in a conductive composition containing a crystalline resin, the spherulites of the crystalline resin grow and expand with age and use conditions such as temperature, and it is difficult to cut the contact point of the conductive material to reduce resistance. There is an increasing phenomenon. However, as in the present application, by adding a substance for making the spherulites fine and uniform, the growth is eliminated, the carbon contact points are not separated, and the resistance is made uniform over a long period of time.
【図面の簡単な説明】 図は本発明の一実施例に示した組成物の抵抗値変化を示
すグラフである。BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a graph showing changes in resistance value of the composition shown in one example of the present invention.
Claims (1)
及び構造式が (但し、RはH,CH3,C2H5、MはAl,Na,K,Ca)で示される
化合物を0.1wt%以上5wt%未満添加して成る導電性樹脂
組成物。1. A crystalline organic binder, carbon powder and structural formula (Wherein, R represents H, CH 3, C 2 H 5, M is Al, Na, K, Ca) compound a conductive resin composition obtained by adding less than 0.1 wt% or more 5 wt% represented by.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28039484A JPH0676511B2 (en) | 1984-12-28 | 1984-12-28 | Conductive resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28039484A JPH0676511B2 (en) | 1984-12-28 | 1984-12-28 | Conductive resin composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61157559A JPS61157559A (en) | 1986-07-17 |
| JPH0676511B2 true JPH0676511B2 (en) | 1994-09-28 |
Family
ID=17624413
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP28039484A Expired - Lifetime JPH0676511B2 (en) | 1984-12-28 | 1984-12-28 | Conductive resin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0676511B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4566313B2 (en) * | 2000-01-25 | 2010-10-20 | 株式会社フジクラ | Conductive ink composition and planar heating element using the same |
-
1984
- 1984-12-28 JP JP28039484A patent/JPH0676511B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61157559A (en) | 1986-07-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |