JPH02100301A - Moisture-sensitive element - Google Patents

Moisture-sensitive element

Info

Publication number
JPH02100301A
JPH02100301A JP63252163A JP25216388A JPH02100301A JP H02100301 A JPH02100301 A JP H02100301A JP 63252163 A JP63252163 A JP 63252163A JP 25216388 A JP25216388 A JP 25216388A JP H02100301 A JPH02100301 A JP H02100301A
Authority
JP
Japan
Prior art keywords
moisture
sensitive element
humidity
porous sintered
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.)
Pending
Application number
JP63252163A
Other languages
Japanese (ja)
Inventor
Noboru Shikatani
鹿谷 昇
Masato Nagano
長野 正登
Kazuhito Narumi
鳴海 一仁
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.)
NOF Corp
Original Assignee
Nippon Oil and Fats 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 Nippon Oil and Fats Co Ltd filed Critical Nippon Oil and Fats Co Ltd
Priority to JP63252163A priority Critical patent/JPH02100301A/en
Publication of JPH02100301A publication Critical patent/JPH02100301A/en
Pending legal-status Critical Current

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  • Investigating Or Analyzing Materials By The Use Of Fluid Adsorption Or Reactions (AREA)
  • Non-Adjustable Resistors (AREA)

Abstract

PURPOSE:To reduce aging and temperature dependency of a resistor by using a porous sintered body ceramic obtained by including a 0.1 to 10mol part of BaCO3 and a 0.01 to 2mol part of Ta2O5 for a main constituent 100 mold part consisting of a 35 to 90mol part of TiO2 and a 10 to 65mol part of SiO2 and then sintering it. CONSTITUTION:A particle weighed with a ratio of a 0.1 to 10mol part of BaCO3 and a 0.01 to 2mol part of Ta2O5 for a main constituent 100mol part consisting of a 35 to 90mol% of TiO2 and a 10 to 65mol% of SiO2 is mixed. Then, after forming it to a specified shape, a porous sintered body ceramic is obtained by sintering it at a temperature of 1250 to 1400 deg.C. A desired humidity sensor can be assembled using this moisure-sensitive element. Thus, it can function within a wide range of detection measurement range (moisture: 5-95% R.H.), thus reducing aging and temperature dependency of a resistor.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、空FiIi機器、湿度制御システムの湿度セ
ンサに好適の感湿素子に関するものである。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a humidity sensing element suitable for a humidity sensor of an aerial FiI device or a humidity control system.

(従来の技術) 従来、この種の湿度センサに用いられる感湿素子として
は、電気抵抗の変化を利用するものがその大部分であり
、中でも金属酸化物の焼結体のセラミックスからなるも
のは、有機物系のものに比較して、材料自体の劣化、耐
熱性等の面で優れている。
(Prior art) Conventionally, most of the humidity sensing elements used in this type of humidity sensor utilize changes in electrical resistance, and among them, those made of ceramics made of sintered metal oxides are Compared to organic materials, it is superior in terms of deterioration of the material itself, heat resistance, etc.

しかしながら、前記セラミックスからなる感湿素子でも
、従来からのものは、初期においては、良好な特性を有
するものであっても、長時間の使用においては、矢張り
経時変化を生じ易いという欠点があった。
However, even if the conventional moisture sensing elements made of ceramics have good characteristics in the initial stage, they have the disadvantage that they tend to deteriorate over time when used for a long time. Ta.

このため焼結体セラミックスの近傍に再生のための加熱
クリーニングヒーターを付設した湿度センサが実用化さ
れている。
For this reason, humidity sensors have been put into practical use that are equipped with heating cleaning heaters for regeneration near the sintered ceramics.

又、組成の金属酸化物は、一般に、負の抵抗温度係数を
有しており、僅かの温度変化に対しても抵抗値が増減す
るため、温度変化が無視できない条件下での湿度の測定
は、誤差が大きくなるという欠点があった。
In addition, metal oxides in the composition generally have a negative temperature coefficient of resistance, and the resistance value increases or decreases even with slight temperature changes, so it is difficult to measure humidity under conditions where temperature changes cannot be ignored. However, there was a drawback that the error was large.

(発明が解決しようとする課題) このように、従来の金属酸化物のセラミックスからなる
感湿素子は、その欠点である経時炭化及び抵抗の温度依
存性を軽減するため、各々加熱クリーニングヒーター、
温度補償回路を必要とし、これらの感湿素子を用いた湿
度センサの寸法を大きくすると共に、電力消費量も大き
くなるという問題を内包するものであった。
(Problems to be Solved by the Invention) As described above, in order to reduce the disadvantages of the conventional moisture sensing element made of metal oxide ceramics, such as carbonization over time and temperature dependence of resistance, heating cleaning heaters, heating cleaning heaters,
This requires a temperature compensation circuit, increases the size of a humidity sensor using these humidity sensing elements, and has the problem of increasing power consumption.

本発明は、このような従来の欠点を解消し、感湿素子、
ひいてはこれを用いた湿度センサとして、湿度に対して
広範な検出及び計測範囲を有し、さらには、前述した経
時変化、抵抗の温度依存性を、それ自体で軽減した感湿
素子及びこれを用いた湿度センサを提供しようとするも
のである。
The present invention eliminates such conventional drawbacks and provides a moisture-sensitive element,
Furthermore, as a humidity sensor using this, it has a wide detection and measurement range for humidity, and furthermore, a humidity sensing element that itself reduces the above-mentioned changes over time and temperature dependence of resistance, and a humidity sensing element using this. The aim is to provide a humidity sensor that is

これにより、従来のような加熱クリーニングヒーターや
特別な温度補償回路を必要としない湿度センサを実現す
ることが可能となる。
This makes it possible to realize a humidity sensor that does not require a conventional cleaning heater or special temperature compensation circuit.

(課題を解決するための手段) 本発明の感湿素子は、Ti0z35〜90モル部と、5
iOxlO〜65モル部とからなる主成分100モル部
に対し、BaC0* 0.1〜10モル部と、Tazo
Bo、01〜2モル部とを配合含有せしめて焼結した多
孔質°焼結体セラミックスからなることを特徴とする。
(Means for Solving the Problems) The moisture sensitive element of the present invention contains 35 to 90 mole parts of TiOz and 5
0.1 to 10 mole parts of BaC0* and Tazo
It is characterized by being made of a porous sintered ceramic body containing 1 to 2 mole parts of Bo and sintered therein.

さらに、これを具体的に得るには、Ti0z35〜90
モル%と510g1O〜65モル%とからなる主成分1
00モル部に対し、B a CO30,1〜10モル部
と、T a z Os 0 、01〜2モル部との割合
で秤量した粉体を混合し、所定の形状に成形した後、温
度1250−1400’Cで焼成することにより、多孔
質焼結体のセラミックスとして得られ、この感湿素子を
用いて所望の湿度センサが組立てられる。
Furthermore, in order to specifically obtain this, Ti0z35~90
Main component 1 consisting of mol% and 510g1O to 65 mol%
Powders weighed at a ratio of 1 to 10 mol parts of B a CO3 and 01 to 2 mol parts of T az Os 0 to 00 mol parts are mixed, molded into a predetermined shape, and heated to a temperature of 1250 mol. By firing at -1400'C, a porous sintered ceramic is obtained, and a desired humidity sensor is assembled using this humidity sensing element.

(作 用) 本発明の感湿素子として、その組成の主成分をTi02
35〜90モル%及び5iOzlO〜65モル%とする
が、ここでT i O2は、感湿素子の基材として作用
し、Singは、焼結体セラミックスとした場合の多孔
質化を促進する働きをする。
(Function) As the moisture sensitive element of the present invention, the main component of its composition is Ti02
35 to 90 mol% and 5iOzlO to 65 mol%, where TiO2 acts as a base material for the moisture-sensitive element, and Sing acts to promote porosity in the case of sintered ceramics. do.

しかして、T i Ozを35モル%未満、すなわち5
iO−を65モル%よりも多くすると、得られる焼結体
セラミックスの抵抗の値が大きくなり、経時での変化率
が増加し、かつ焼結体セラミックスの強度も低下するた
め好ましくない。又、逆に、T i Otが90モル%
を越える場合、すなわち、S i Ozが10モル%未
満になる場合には、抵抗の温度依存性が大きくなると共
に、得られる焼結体セラミックスの多孔質化が不充分と
なって気孔率が減少するため、湿度変化に対する抵抗の
変化の傾向が鈍化し好ましくない。
Thus, T i Oz is less than 35 mol %, i.e. 5
If iO- is more than 65 mol%, the resistance value of the resulting sintered ceramic becomes large, the rate of change over time increases, and the strength of the sintered ceramic decreases, which is not preferable. Also, conversely, T i Ot is 90 mol%
If the SiOz exceeds 10% by mole, the temperature dependence of resistance increases and the resulting sintered ceramic becomes insufficiently porous, resulting in a decrease in porosity. Therefore, the tendency of resistance change with respect to humidity change becomes slower, which is undesirable.

次に、添加成分について、BaCO3は、焼結体セラミ
ックスの粒子成長を抑制し気孔率を高める作用を有する
。従って、B a COsが、T i Oを及びSto
wからなる主成分100モル部に対し、0.1モル部を
下回ると、粒子径が大となり気孔率が低下するため、湿
度変化に対する抵抗の変化の傾向が鈍化し、かつ、抵抗
の温度依存性が大きくなってしまう。一方、B a C
Osが10モル部を越える場合には、焼結体セラミック
スの抵抗値が大きくなるため好ましくない。
Next, regarding the additive components, BaCO3 has the effect of suppressing grain growth and increasing the porosity of the sintered ceramic. Therefore, B a COs, T i O and Sto
When it is less than 0.1 mole part per 100 mole parts of the main component consisting of w, the particle size becomes large and the porosity decreases, so the tendency of resistance change with respect to humidity changes becomes slower, and the temperature dependence of resistance decreases. Sexuality becomes larger. On the other hand, B a C
If Os exceeds 10 mole parts, the resistance value of the sintered ceramic becomes large, which is not preferable.

次に、Taxesは、TiO□に対する原子価制御剤と
して働き、上記の主成分100モル部に対し、0.01
モル部を下回った場合には、焼結体セラミックスの抵抗
値が大きくなるため好ましくない。又、2モル部を越え
た場合には、焼結体の抵抗値が大きくなるため、好まし
くない。
Next, Taxes acts as a valence control agent for TiO□, and 0.01 parts by mole of the above main component
If it is less than the molar part, the resistance value of the sintered ceramic becomes large, which is not preferable. Moreover, if it exceeds 2 molar parts, the resistance value of the sintered body becomes large, which is not preferable.

以上述べたように、TtO,は、本発明の感湿素子の基
材を構成するが、これに上記の所定量のS i Ot 
1B a CO3及びTatOsを同時に添加すること
によって、はじめて優れた感湿特性を発現することがで
きたのである。
As described above, TtO constitutes the base material of the moisture-sensitive element of the present invention, and the above-mentioned predetermined amount of S i Ot
By simultaneously adding 1B a CO3 and TatOs, it was possible to develop excellent moisture sensitivity properties.

以下本発明をさらに実施例について説明する。The present invention will be further described below with reference to Examples.

(実施例) 第1表に示す試料陽、1〜20について、各組成を持つ
ように、各成分原料を秤量し、湿式のボールミルで12
時間混合した。この混合物を乾燥した後、少量のポリビ
ニルアルコールからなるバインダーを加えて撹拌した。
(Example) For samples 1 to 20 shown in Table 1, each component raw material was weighed so as to have each composition, and 12
Mixed for an hour. After drying this mixture, a small amount of a binder consisting of polyvinyl alcohol was added and stirred.

次に、80メツシユの篩を通過させて造粒粉を得た。こ
の造粒粉を1 ton 7cm”の圧力で、直径10I
III11、厚さ0.8 mmの円板状に成形した。次
に、これを空気中で温度1350°Cにて、1時間焼成
し多孔質の焼結体セラミックスを得た。
Next, the powder was passed through an 80 mesh sieve to obtain granulated powder. This granulated powder was heated to a diameter of 10 mm at a pressure of 1 ton 7 cm.
III11, and was molded into a disk shape with a thickness of 0.8 mm. Next, this was fired in air at a temperature of 1350° C. for 1 hour to obtain a porous sintered ceramic.

次いで、この焼結体セラミックスの両面にRuO□ペー
ストを焼付け、リード線付は等の処理を施こし、一対の
電極を設けた。
Next, RuO□ paste was baked on both sides of this sintered ceramic body, and lead wires were attached and a pair of electrodes were provided.

このようにして得られた各試料につき、それぞれの感湿
特性を電気抵抗の測定から求めた。その結果も第1表に
まとめて示した。
The moisture sensitivity characteristics of each sample thus obtained were determined by measuring electrical resistance. The results are also summarized in Table 1.

(発明の効果) 本発明の多孔質焼結体セラミックスからなる感湿素子は
、湿度5〜95%(R,t(、)と広範な検知計測範囲
で機能し、経時変化、抵抗の温度依存性を軽減したもの
であり、これを具備してなる湿度センサは、小型で高精
度であるため利用価値が極めて大きい。
(Effects of the Invention) The humidity sensing element made of the porous sintered ceramic of the present invention functions in a wide detection and measurement range of humidity 5 to 95% (R, t(,), and exhibits resistance change over time and temperature dependence. A humidity sensor equipped with this is small and highly accurate, and has extremely high utility value.

Claims (1)

【特許請求の範囲】[Claims] 1.TiO_2 35〜90モル部と、SiO_2 1
0〜65モル部とからなる主成分100モル部に対し、
BaCO_3 0.1〜10モル部と、Ta_2O_5
 0.01〜2モル部とを配合含有せしめて焼結した多
孔質焼結体セラミックスからなることを特徴とする感湿
素子。
1. 35 to 90 mole parts of TiO_2 and 1 part of SiO_2
For 100 mole parts of the main component consisting of 0 to 65 mole parts,
0.1 to 10 mole parts of BaCO_3 and Ta_2O_5
1. A moisture-sensitive element comprising a porous sintered ceramic containing 0.01 to 2 mole parts of the porous sintered ceramic.
JP63252163A 1988-10-07 1988-10-07 Moisture-sensitive element Pending JPH02100301A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63252163A JPH02100301A (en) 1988-10-07 1988-10-07 Moisture-sensitive element

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63252163A JPH02100301A (en) 1988-10-07 1988-10-07 Moisture-sensitive element

Publications (1)

Publication Number Publication Date
JPH02100301A true JPH02100301A (en) 1990-04-12

Family

ID=17233363

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63252163A Pending JPH02100301A (en) 1988-10-07 1988-10-07 Moisture-sensitive element

Country Status (1)

Country Link
JP (1) JPH02100301A (en)

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