JPS60106101A - Polymer temperature sensor - Google Patents

Polymer temperature sensor

Info

Publication number
JPS60106101A
JPS60106101A JP21324383A JP21324383A JPS60106101A JP S60106101 A JPS60106101 A JP S60106101A JP 21324383 A JP21324383 A JP 21324383A JP 21324383 A JP21324383 A JP 21324383A JP S60106101 A JPS60106101 A JP S60106101A
Authority
JP
Japan
Prior art keywords
polyamide
temperature
ferric chloride
present
weight
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
JP21324383A
Other languages
Japanese (ja)
Other versions
JPH0244123B2 (en
Inventor
喜多 雅美
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.)
Daicel Evonik Ltd
Original Assignee
Daicel Huels 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 Daicel Huels Ltd filed Critical Daicel Huels Ltd
Priority to JP21324383A priority Critical patent/JPH0244123B2/en
Publication of JPS60106101A publication Critical patent/JPS60106101A/en
Publication of JPH0244123B2 publication Critical patent/JPH0244123B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Thermistors And Varistors (AREA)
  • Compositions Of Macromolecular Compounds (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】 本発明は、特定のポリアミド樹脂組成物からなる熱感応
性材料、特に電気容量成分を一つの制御因子として熱制
御する装置における熱感応性材料の温度lこ対する抵抗
値やインピーダンスの挙動が改善された材料に関するも
のである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a heat-sensitive material made of a specific polyamide resin composition, and particularly to a device for thermally controlling a capacitance component as one control factor. and materials with improved impedance behavior.

従来から、温度による電気的性質の変化の大きい有機高
分子材料、例えばポリ塩化ビニル、ポリアミドなどを熱
感応性素子として使用することは、電気毛布、電気カー
ペットなどの例によって知られている。熱感応性素子の
制御因子としては、直流体積固有抵抗、比誘電率および
体積固有インピーダンスなどがあり、これらの−〇また
はそれ以上の組合せてもって制御面路を作動させるこ七
ができる。したがっそ、熱感応性素子に要求、される特
性として、は、温度による電気的性質の変化が大きいこ
と、吸湿による電気的性質の変化が小さいこと、ヒート
サイク”ルによる電気的性質の経時的変化がなく安定で
あることなどが挙げられる。
BACKGROUND ART The use of organic polymeric materials whose electrical properties change significantly depending on temperature, such as polyvinyl chloride and polyamide, as heat-sensitive elements has been known from the past, as seen in electric blankets, electric carpets, and the like. Control factors for the thermosensitive element include direct current volume resistivity, dielectric constant, and volume resistivity, and the control surface path can be operated by a combination of -0 or more of these. Therefore, the characteristics required of a thermosensitive element are: large changes in electrical properties due to temperature, small changes in electrical properties due to moisture absorption, and changes in electrical properties over time due to heat cycling. For example, it is stable and free of oxidation.

これまで、この種の目的に合うようにするため、上記の
有機高分子材料に添加剤として界面活性剤などのイオン
電導性物質を添加したり(特開昭35−14179)、
イオン解離しゃすいハロゲン化銅などを添加していた(
特開昭56−3904)。
Until now, in order to meet this type of purpose, ion conductive substances such as surfactants have been added to the above organic polymer materials as additives (Japanese Patent Application Laid-Open No. 35-14179),
Copper halides, etc., which are ionically dissociable, were added (
Japanese Patent Publication No. 56-3904).

出ころがこれら組成物の電導キ、ヤリャは当然イオン性
物質であるため、直流電場を印加すると分極を起こし、
インピーダンスの大きな経時変化を引き起こしてしまい
、また特に前者は耐熱性の点で劣るため、後述のような
感熱上−ターの感温体としては使用できなかった。
The main reason for the conductivity of these compositions is that they are naturally ionic substances, so when a DC electric field is applied, they cause polarization.
This causes a large change in impedance over time, and the former particularly has poor heat resistance, so it could not be used as a thermosensitive body as described below.

そこで本発明は、上述した実用上のいくつかの問題点を
解決すべく鋭意検・討した結果、特定のポリアミド樹脂
と特定の添加剤の組合せにより、上記要求性能を満足す
る熱感応性材料を作り得ることを見出し、本発明に到、
達した。
Therefore, as a result of intensive study and study to solve some of the above-mentioned practical problems, the present invention has developed a heat-sensitive material that satisfies the above-mentioned performance requirements by combining a specific polyamide resin and a specific additive. discovered that it could be made, and came up with the present invention,
Reached.

すなわち、本発明は炭素原子数100個当りのアミド基
数が14個以下のポリアミド樹脂に塩化第ニ鉄を0.1
〜1O10重量部配合したポリアミド組成物からなる熱
感応性材料を提供するものである。
That is, in the present invention, 0.1 ferric chloride is added to a polyamide resin having 14 or less amide groups per 100 carbon atoms.
The present invention provides a heat-sensitive material comprising a polyamide composition containing 10 parts by weight of 1O.

本発明における熱感応性材料よりなる熱感応性素子によ
れば、温度に対する電気的性質の変化率が著しく大きく
、界面活性剤のようにブリードアウトしたり、劣化した
りして経時変化することもないため、電気的性質の安定
性がすぐわでおり、史には信号導体に用いられるアル、
ミニラム、銅などの金属線または金属箔を腐食すること
がなく、耐熱性が優れ、またポリアミド樹脂と塩化第二
鉄との混練が容易であるなどの利点が得られる。
According to the heat-sensitive element made of the heat-sensitive material of the present invention, the rate of change in electrical properties with respect to temperature is extremely large, and unlike surfactants, it may bleed out or deteriorate over time. Because there is no aluminum, its electrical properties are very stable, and there is a history of aluminum used for signal conductors.
It does not corrode metal wires or metal foils such as minilum, copper, etc., has excellent heat resistance, and has advantages such as easy kneading of polyamide resin and ferric chloride.

本発明で使用するポリアミド樹脂とは、ポリアミノウン
デカミド(ナイロン11)あるいはポリω−ラウロラク
タム(ナイロン12)で代表される′アミド基濃度の低
いポリアミド、更に詳しく述べるならば炭素原子数io
o個当りのアミド基数が14個以下のホモポリアミドま
たはコポリアミドである。
The polyamide resin used in the present invention is a polyamide with a low concentration of amide groups such as polyaminoundecamide (nylon 11) or polyω-laurolactam (nylon 12), and more specifically, a polyamide with a carbon atom number of io
It is a homopolyamide or copolyamide in which the number of amide groups per o is 14 or less.

本発明における熱感応性素子用ポリアミド組成物の添加
剤成分である塩化第二鉄の添加量は、0.1〜10.0
重量部、好まLl’ <は0.5〜’5.0重量部が適
当であり、0.1重量部以下では電気的性質の温度に対
する変化が十分でなく、10.0重量部以上ではポリア
ミド樹脂の機械的性質が低下してしすうため好ましくな
い。
The amount of ferric chloride, which is an additive component of the polyamide composition for heat-sensitive elements in the present invention, is 0.1 to 10.0.
Parts by weight, preferably 0.5 to 5.0 parts by weight. If it is less than 0.1 parts by weight, the change in electrical properties with respect to temperature is insufficient, and if it is more than 10.0 parts by weight, the polyamide This is not preferable because the mechanical properties of the resin deteriorate.

塩化第二鉄をポリアミド樹脂に添加する方法は特に限定
されず、ポリアミドの重合段階で添加する方法、ポリア
ミドの粉末と塩化第二鉄を機械的に混合する方法、ある
いは、ポリアミドペレットと塩化第二鉄を混合後押出機
で溶融混練する方法など任意の方法が実施できる。
The method of adding ferric chloride to the polyamide resin is not particularly limited, and may be a method of adding it during the polyamide polymerization step, a method of mechanically mixing polyamide powder and ferric chloride, or a method of adding ferric chloride with polyamide pellets. Any method can be used, such as mixing iron and then melting and kneading it in an extruder.

塩化第二鉄を含有するポリアミド組成物は、通常さらに
押出機などによって線あるいはシートの形状に成形して
熱感応性素子とされる。
The polyamide composition containing ferric chloride is usually further formed into a wire or sheet shape using an extruder or the like to form a heat-sensitive element.

以下本発明の効果を実施例をもって説明する。The effects of the present invention will be explained below using examples.

実施例1 ナイロン12ペレット(ダイセルヒュルス製「ダイアミ
ドLI901J)100重量部に対し、塩化第二鉄1重
量部をトライブレンドした後、押出機を用いてこれらを
溶融混練し、ペレタイザーニヨッてペレット化した。こ
のペレッ) % 220’で圧縮成形により厚み約o、
5mmのシートを作成した。このシートの100QHz
における体積固有インピータンスの温度依存性を測定し
た。その結果は、第1図の曲線Aで示すように非常ζζ
大きな勾配が得られた。
Example 1 After tri-blending 1 part by weight of ferric chloride with 100 parts by weight of nylon 12 pellets (Diamid LI901J manufactured by Daicel Huls), they were melt-kneaded using an extruder and made into pellets using a pelletizer. The pellets were compressed to a thickness of approximately 0, % 220',
A 5 mm sheet was created. 100QHz of this sheet
The temperature dependence of the specific volume impedance was measured. The result is extremely ζζ, as shown by curve A in Figure 1.
A large gradient was obtained.

実施例2 塩化第二鉄を水に完全に溶解した後、ナイロン6・12
粉末(タ゛イセルヒュルス製「ダイアミドD170oJ
’)100重量部に対し、塩化第二鉄を5重量部の割合
でヘンシェルミキサーで混合した後、水を完全に蒸発さ
せた。この粉末Tr 220’で圧縮成形により厚み約
0.5朋のシートを作成し、実施例1と同様にして゛体
積固有インピーダンスを測定した。結果は第1図の曲線
Bで示すように。
Example 2 After completely dissolving ferric chloride in water, nylon 6/12
Powder (“Diamid D170oJ” made by Teiselhuls)
') After mixing 5 parts by weight of ferric chloride to 100 parts by weight using a Henschel mixer, water was completely evaporated. A sheet with a thickness of about 0.5 mm was prepared by compression molding using this powdered Tr 220', and its volumetric impedance was measured in the same manner as in Example 1. The results are shown by curve B in Figure 1.

実施例1と同様良好な温度勾配を持っている。Like Example 1, it has a good temperature gradient.

比較例1 実施例11こおいてナイロン12ペレツ) K 塩化第
二鉄を混入しないこと以外は実施例1と全く同様にして
厚さ約0.5龍のシートを作1.す1、温度・インピー
ダンス特性を調べたところ、第1図の曲線Clζ示すよ
うに、本発明に比べて勾配がゆるくなっていることがわ
かる〇 比較例2 実施例1において、ナイロン6@12ベレン)を使い、
塩化第二鉄を混入しないこと以外は実施例1と全く同、
様にして、厚さ約0.5龍のソートを作り、温度・イン
ピータンス特性を調べたところ第1−の曲線りのように
なり本発明に比べ勾配がゆるくなっていることがわかる
Comparative Example 1 A sheet with a thickness of approximately 0.5 mm was made in the same manner as in Example 1 except that ferric chloride was not mixed (Nylon 12 pellets in Example 11). 1. When the temperature/impedance characteristics were investigated, it was found that the slope was gentler than that of the present invention, as shown by the curve Clζ in Figure 1. Comparative Example 2 In Example 1, nylon 6@12 belene ),
Exactly the same as Example 1 except that ferric chloride was not mixed.
When a sort with a thickness of approximately 0.5 mm was prepared in the same manner and the temperature/impedance characteristics were examined, it was found that the slope was similar to that of the 1-th curve, and the slope was gentler than that of the present invention.

これらの結果かられかるように、本発明の感温体はナイ
ロン12や、ナイロン6・12単独のものに比べ、温度
検知機能、すなわちインピーダンスの温度に対する変化
率が非常に改善されており、すぐれた電気的性質を有し
ている。
As can be seen from these results, the temperature sensing element of the present invention has a significantly improved temperature detection function, that is, the rate of change in impedance with respect to temperature, compared to nylon 12 or nylon 6/12 alone. It has good electrical properties.

【図面の簡単な説明】[Brief explanation of drawings]

lEJ図は本発明の実施例および比較例により得られた
高分子感温体の体積固有インピータンスと温度の関係を
示すグラフである。 特許出願人 タイセル・ヒュルス株式会社20 40 
60 80 100 120 140温 度 (℃)
The lEJ diagram is a graph showing the relationship between the volume-specific impedance and temperature of the polymer thermosensitive bodies obtained in Examples and Comparative Examples of the present invention. Patent applicant Tyssel-Hüls Co., Ltd. 20 40
60 80 100 120 140 Temperature (℃)

Claims (1)

【特許請求の範囲】[Claims] 炭素原子数100個当たりのアミド基数が14個以下の
ポリアミド樹脂Cζ塩化第二鉄’0.1〜10.0重量
部配合したポリアミド組成物からなる高分子感温体
A polymer thermosensitive body made of a polyamide composition containing 0.1 to 10.0 parts by weight of a polyamide resin Cζferric chloride having 14 or less amide groups per 100 carbon atoms.
JP21324383A 1983-11-15 1983-11-15 KOBUNSHIKANONTAI Expired - Lifetime JPH0244123B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21324383A JPH0244123B2 (en) 1983-11-15 1983-11-15 KOBUNSHIKANONTAI

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21324383A JPH0244123B2 (en) 1983-11-15 1983-11-15 KOBUNSHIKANONTAI

Publications (2)

Publication Number Publication Date
JPS60106101A true JPS60106101A (en) 1985-06-11
JPH0244123B2 JPH0244123B2 (en) 1990-10-02

Family

ID=16635883

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21324383A Expired - Lifetime JPH0244123B2 (en) 1983-11-15 1983-11-15 KOBUNSHIKANONTAI

Country Status (1)

Country Link
JP (1) JPH0244123B2 (en)

Also Published As

Publication number Publication date
JPH0244123B2 (en) 1990-10-02

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