JPH11326259A - Inorganic composition for carbon dioxide sensor, manufacture of carbon dioxide sensor and carbon dioxide sensor obtained by it - Google Patents
Inorganic composition for carbon dioxide sensor, manufacture of carbon dioxide sensor and carbon dioxide sensor obtained by itInfo
- Publication number
- JPH11326259A JPH11326259A JP12570798A JP12570798A JPH11326259A JP H11326259 A JPH11326259 A JP H11326259A JP 12570798 A JP12570798 A JP 12570798A JP 12570798 A JP12570798 A JP 12570798A JP H11326259 A JPH11326259 A JP H11326259A
- Authority
- JP
- Japan
- Prior art keywords
- carbon dioxide
- inorganic composition
- dioxide gas
- dioxide sensor
- sensor
- Prior art date
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- Investigating Or Analyzing Materials By The Use Of Fluid Adsorption Or Reactions (AREA)
- Investigating Or Analyzing Materials By The Use Of Electric Means (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、室内や車内等の居
住空間の空気汚染モニタ、空調システム用モニタ、生鮮
食料品の輸送・保管時の炭酸ガス濃度制御装置、バイオ
施設での炭酸ガス濃度モニタシステム等に用いられる炭
酸ガスセンサ用無機組成物及びそれを用いた炭酸ガスセ
ンサの製造方法及びそれにより得られた炭酸ガスセンサ
に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a monitor for air pollution in a living space such as a room or a car, a monitor for an air conditioning system, a carbon dioxide concentration control device for transporting and storing fresh foods, and a carbon dioxide concentration in a bio facility. The present invention relates to an inorganic composition for a carbon dioxide sensor used for a monitor system or the like, a method for producing a carbon dioxide sensor using the same, and a carbon dioxide sensor obtained by the method.
【0002】[0002]
【従来の技術】近年、環境測定、施設園芸、生産設備等
に炭酸ガス濃度を検知する炭酸ガスセンサが用いられて
いる。炭酸ガスセンサとしては赤外線を用いた検知方
法、電解液を使用した方法、熱伝導を利用した方法によ
る測定器が市販されているが、大型であり、製造コスト
が嵩んでいる。このため、他の方法が検討されており、
NaCO3を電極としNASICON等のアルカリイオ
ン導電性固体電解質を用いた方法、Liイオン導電体を
用いた方法、K2CO3等のCO32-イオン導電体を用い
た方法、水酸化アパタイトの抵抗値を用いる方法等、様
々な検知方法による新しいタイプの炭酸ガスセンサの研
究開発が行われている。2. Description of the Related Art In recent years, a carbon dioxide sensor for detecting a carbon dioxide concentration has been used in environmental measurement, facility horticulture, production equipment, and the like. As a carbon dioxide sensor, a measuring method using a detection method using infrared rays, a method using an electrolytic solution, and a method using heat conduction are commercially available, but are large in size and the manufacturing cost is high. For this reason, other methods are being considered,
A method using an alkali ion conductive solid electrolyte such as NASICON using NaCO 3 as an electrode, a method using a Li ion conductor, a method using a CO 32 -ion conductor such as K 2 CO 3 , resistance of hydroxyapatite Research and development of a new type of carbon dioxide sensor using various detection methods, such as a method using a value, has been conducted.
【0003】また、装置の小型化が可能な炭酸ガスセン
サの一つとして、金属酸化物と炭酸塩等の混合物の焼結
体と一対の電極とを組み合わせた構造を有し、焼結体を
構成する非複合系酸化物と炭酸ガスとの可逆的な炭酸塩
形成反応による電極間のインピーダンスや静電容量等の
電気的特性を変化させて炭酸ガス濃度を検知するものが
ある。Further, as one of the carbon dioxide sensors capable of miniaturizing the apparatus, the carbon dioxide sensor has a structure in which a sintered body of a mixture of a metal oxide and a carbonate and the like and a pair of electrodes are combined to form a sintered body. There is a method of detecting the concentration of carbon dioxide by changing electrical characteristics such as impedance and capacitance between electrodes by a reversible carbonate formation reaction between the non-composite oxide and carbon dioxide.
【0004】例えば、特開平4−24548には「ペロ
ブスカイト型金属酸化物と非複合系金属酸化物との混合
物の静電容量の変化を用いた炭酸ガスセンサ」、特願平
6−182261には「非複合系金属酸化物の混合物を
用いた炭酸ガスセンサ」、特開平6−88800には
「非複合系金属酸化物の一種である希土類酸化物を用い
た炭酸ガスセンサ」がそれぞれ開示されている。For example, Japanese Patent Application Laid-Open No. 4-24548 discloses a "carbon dioxide sensor using a change in capacitance of a mixture of a perovskite-type metal oxide and a non-composite metal oxide". A carbon dioxide sensor using a mixture of non-composite metal oxides ”and JP-A-6-88800 disclose a“ carbon dioxide sensor using a rare earth oxide that is a kind of non-composite metal oxides ”.
【0005】これらのセンサは例えばCuO、BaTi
O3等の市販原料または市販原料を混合後熱処理して作
製した原料を用いて作製される。使用される原料は所定
の混合比になるよう混合粉砕された後、成型、熱処理さ
れ板状の炭酸ガス感知セラミックからなる炭酸ガス検知
部本体が作製される。その後、炭酸ガス濃度の変化に伴
う電気的変化を調べるため、電気信号取り出し用の電極
部が作製されて炭酸ガスセンサとなる。炭酸ガスの検知
は静電容量の変化、またはインピーダンスの変化により
なされる。これらの炭酸ガスセンサの検知能力向上のた
め特開平5−142180ではAg等の貴金属元素、遷
移金属元素の添加を、特願平6−313410ではBa
Oの添加を、特願平7−165053では炭酸塩の添加
を提案されている。[0005] These sensors are, for example, CuO, BaTi
It is manufactured using a commercially available raw material such as O 3 or a raw material prepared by mixing and then heat treating a commercially available raw material. The raw materials to be used are mixed and pulverized so as to have a predetermined mixing ratio, and then molded and heat-treated to produce a carbon dioxide gas detecting portion main body made of a plate-like carbon dioxide gas sensing ceramic. Thereafter, in order to examine an electrical change accompanying a change in the concentration of carbon dioxide, an electrode portion for extracting an electric signal is manufactured, and a carbon dioxide sensor is obtained. The detection of carbon dioxide is performed by a change in capacitance or a change in impedance. In order to improve the detection performance of these carbon dioxide sensors, addition of a noble metal element or a transition metal element such as Ag is disclosed in JP-A-5-142180, and Ba is disclosed in Japanese Patent Application No. 6-313410.
The addition of O is proposed in Japanese Patent Application No. 7-165053.
【0006】[0006]
【発明が解決しようとする課題】しかしながら、上記従
来の非複合系金属酸化物、炭酸塩の混合物の焼結体を用
いた炭酸ガスセンサは、低濃度の炭酸ガスに対する検知
感度が小さいという課題を有していた。また、個々の炭
酸ガスセンサの静電容量値にばらつきが大きいという課
題を有していた。However, the conventional carbon dioxide gas sensor using a sintered body of a mixture of a non-composite metal oxide and a carbonate has a problem that the detection sensitivity to low-concentration carbon dioxide is small. Was. Also, there is a problem that the capacitance values of the individual carbon dioxide sensors vary widely.
【0007】本発明は上記従来の課題を解決するもので
あり、低濃度の炭酸ガスの検知感度が高く、静電容量値
の安定した炭酸ガスセンサ用無機組成物の提供、及び高
品質かつ安定した品質で低原価で量産できる炭酸ガスセ
ンサ用無機組成物及びそれを用いた炭酸ガスセンサの製
造方法及びそれにより得られた炭酸ガスセンサの提供を
目的とする。SUMMARY OF THE INVENTION The present invention has been made to solve the above-mentioned conventional problems, and provides an inorganic composition for a carbon dioxide sensor having a high detection sensitivity for a low concentration of carbon dioxide and a stable capacitance value. It is an object of the present invention to provide an inorganic composition for a carbon dioxide sensor that can be mass-produced at high quality at low cost, a method for manufacturing a carbon dioxide sensor using the same, and a carbon dioxide sensor obtained by the method.
【0008】[0008]
【課題を解決するための手段】本発明の炭酸ガスセンサ
用無機組成物は、CeO2、BaCO3、CuOを含有す
る炭酸ガスセンサ用無機組成物であって、CeO2、B
aCO3、CuOのモル比を、CeO2=A、BaCO3
=B、CuO=Cとし、A+B+C=100モル%とし
たときにA、B及びCを制御された構成を備えている。Carbon dioxide sensor for inorganic composition of the present invention SUMMARY OF THE INVENTION is a CeO 2, BaCO 3, carbon dioxide sensor for inorganic composition containing CuO, CeO 2, B
The molar ratio of aCO 3 and CuO is expressed as CeO 2 = A, BaCO 3
= B, CuO = C, and A, B, and C are controlled when A + B + C = 100 mol%.
【0009】この構成により、粒径及び反応性が均質な
酸化物及び炭酸塩からなる粉末を得ることが可能とな
る。このような組成が均一で粒径及び反応性が均質な酸
化物及び炭酸塩からなる粉末を用いた焼結体からなる炭
酸ガスセンサの炭酸ガス検知部を用いることによって、
炭酸ガスの検知感度が高く、静電容量値の安定した炭酸
ガスセンサを与えるとともに、高品質かつ安定した品質
で低原価で量産できる炭酸ガスセンサ用無機組成物を実
現することができる。With this configuration, it is possible to obtain a powder composed of oxides and carbonates having a uniform particle size and reactivity. By using a carbon dioxide gas detection unit of a carbon dioxide gas sensor made of a sintered body using a powder composed of oxides and carbonates having a uniform composition, a uniform particle size and reactivity,
In addition to providing a carbon dioxide gas sensor having high detection sensitivity for carbon dioxide gas and a stable capacitance value, it is possible to realize an inorganic composition for a carbon dioxide gas sensor that can be mass-produced at a low cost with high quality and stable quality.
【0010】また、本発明の炭酸ガスセンサの製造方法
は、CeO2、BaCO3、CuOのモル比を制御したも
のの混合物を、0.3〜2.5t/cm2、好ましくは
0.5〜2t/cm2の圧力で成型した後、750〜1
100℃、好ましくは850〜1000℃の温度で焼成
する工程を有している。The method of manufacturing a carbon dioxide gas sensor according to the present invention is characterized in that a mixture of CeO 2 , BaCO 3 , and CuO having a controlled molar ratio is used in an amount of 0.3 to 2.5 t / cm 2 , preferably 0.5 to 2 t. / Cm 2 at a pressure of 750-1
A step of firing at a temperature of 100 ° C, preferably 850 to 1000 ° C.
【0011】これにより、炭酸ガスの検知感度が高く、
高品質かつ安定した品質で量産性に優れた炭酸ガスセン
サを効率よく生産できる炭酸ガスセンサの製造方法を実
現できる。As a result, the carbon dioxide gas detection sensitivity is high,
A method of manufacturing a carbon dioxide gas sensor capable of efficiently producing a carbon dioxide gas sensor having high quality, stable quality, and excellent mass productivity can be realized.
【0012】また、本発明の炭酸ガスセンサは、所定の
組成比のCeO2、BaCO3、CuO無機組成物の粉末
を、湿式混合、粉砕、成型、焼成した焼結体からなる炭
酸ガス検知部と、炭酸ガス検知部上に配設された静電容
量値の電気信号取り出し用の電極と、を備えた構成より
なる。Further, the carbon dioxide gas sensor of the present invention is provided with a carbon dioxide gas detecting portion comprising a sintered body obtained by wet mixing, pulverizing, molding and firing powders of CeO 2 , BaCO 3 and CuO inorganic compositions having a predetermined composition ratio. And an electrode for extracting an electric signal of a capacitance value provided on the carbon dioxide gas detection unit.
【0013】この構成により、炭酸ガス検知部を構成す
る無機組成物の分布が均一であるため炭酸ガスの検知感
度が高く、かつ粒径及び反応性が均質であるので炭酸ガ
スを検知する界面の状態や粒子密度が均一で、安定した
静電容量値を示すために検知特性のばらつきの少ない信
頼性の高い炭酸ガスセンサを提供することができる。With this configuration, the distribution of the inorganic composition constituting the carbon dioxide gas detecting section is uniform, so that the sensitivity of detecting the carbon dioxide gas is high. It is possible to provide a highly reliable carbon dioxide gas sensor having a uniform state and particle density and exhibiting a stable capacitance value and little variation in detection characteristics.
【0014】[0014]
【発明の実施の形態】本発明の請求項1に記載の炭酸ガ
スセンサ用無機組成物は、CeO2、BaCO3、CuO
を含有する炭酸ガスセンサ用無機組成物であって、Ce
O2、BaCO3、CuOのモル比を、CeO2=A、B
aCO3=B、CuO=Cとし、A+B+C=100モ
ル%としたときに、Aのモル%が45≦A≦95、好ま
しくは50≦A≦90の範囲にあることとしたものであ
り、これにより、炭酸ガスの検知感度が高く、静電容量
値が安定するという作用を有する。BEST MODE FOR CARRYING OUT THE INVENTION The inorganic composition for a carbon dioxide sensor according to the first aspect of the present invention comprises CeO 2 , BaCO 3 , CuO
An inorganic composition for a carbon dioxide sensor containing
The molar ratio of O 2 , BaCO 3 , and CuO is expressed as CeO 2 = A, B
When aCO 3 = B, CuO = C, and A + B + C = 100 mol%, the mol% of A is in the range of 45 ≦ A ≦ 95, preferably 50 ≦ A ≦ 90. Therefore, the carbon dioxide gas detection sensitivity is high and the capacitance value is stabilized.
【0015】ここで、Aが45よりも小さくなるにつれ
て、炭酸ガスセンサ用無機組成物の静電容量値が不安定
になる傾向を生じ、95よりも大きくなるにつれて炭酸
ガス検知感度が低下する傾向を生じるため、いずれも好
ましくない。Here, as A becomes smaller than 45, the capacitance value of the inorganic composition for a carbon dioxide sensor tends to become unstable, and as it becomes larger than 95, the carbon dioxide detection sensitivity tends to decrease. All of these are undesirable.
【0016】本発明の請求項2に記載の炭酸ガスセンサ
用無機組成物は、請求項1に記載の発明において、Cの
モル%がBに対し1.5B≦C≦2.5Bの範囲にある
こととしたものであり、これにより、請求項1に記載の
発明で得られる作用の他、炭酸ガスの検知感度を向上さ
せ、特に感度特性を安定にすることができるという作用
を有する。In the inorganic composition for a carbon dioxide gas sensor according to a second aspect of the present invention, in the invention according to the first aspect, the mole% of C is in the range of 1.5B ≦ C ≦ 2.5B with respect to B. Accordingly, in addition to the effect obtained by the first aspect of the present invention, there is an effect that the detection sensitivity of carbon dioxide gas can be improved, and in particular, the sensitivity characteristics can be stabilized.
【0017】ここで、Cのモル%がBの1.5倍よりも
小さくなるにつれて検知感度が低下する傾向を生じ、B
の2.5倍よりも大きくなるにつれて感度特性が不安定
になる傾向を生じるため、いずれも好ましくない。Here, as the mole% of C becomes smaller than 1.5 times B, the detection sensitivity tends to decrease.
Since the sensitivity characteristic tends to become unstable as the ratio becomes larger than 2.5 times, both are not preferable.
【0018】本発明の請求項3に記載の炭酸ガスセンサ
用無機組成物は、請求項1または2の内のいずれか1に
記載の発明において、CeO2、BaCO3、CuOを含
有する炭酸ガスセンサ用無機組成物の原料粉末の粒径が
0.1μm以上2μm以下の粒子で構成される混合粉末
であることとしたものであり、これにより、粒子の凝集
を防止できるとともに、検知特性のばらつきを抑制する
ことができるという作用を有する。According to a third aspect of the present invention, there is provided the inorganic composition for a carbon dioxide gas sensor according to any one of the first and second aspects, wherein the inorganic composition contains CeO 2 , BaCO 3 , and CuO. The particle size of the raw material powder of the inorganic composition is a mixed powder composed of particles having a particle size of 0.1 μm or more and 2 μm or less, whereby the aggregation of the particles can be prevented and the variation in the detection characteristics is suppressed. Has the effect of being able to
【0019】ここに、原料粉末の粒径が、0.1μmよ
りも小さくなるにつれて粒子が凝集する傾向を生じ、2
μmよりも大きくなるにつれて組成分布が生じ特性がば
らつくという傾向を生じるため、いずれも好ましくな
い。Here, as the particle size of the raw material powder becomes smaller than 0.1 μm, the particles tend to agglomerate,
Since the composition distribution tends to increase as the particle size becomes larger than μm, the characteristics tend to vary.
【0020】本発明の請求項4に記載の炭酸ガスセンサ
の製造方法は、請求項1乃至3の内いずれか1に記載の
炭酸ガスセンサ用無機組成物を粉砕後、0.3〜2.5
t/cm2、好ましくは0.5〜2t/cm2の圧力で所
定の形状に成型する成型工程と、前記成型工程で成型さ
れた成型物を750〜1100℃、好ましくは850〜
1000℃の温度で加熱して焼結する焼結する焼成工程
と、を備えたものであり、これにより、炭酸ガスセンサ
の静電容量値が安定するという作用を有する。According to a fourth aspect of the present invention, there is provided a method for producing a carbon dioxide gas sensor, wherein the inorganic composition for a carbon dioxide gas sensor according to any one of the first to third aspects is pulverized and then pulverized to 0.3 to 2.5.
t / cm 2, preferably 0.5~2T / a molding process in which a pressure of cm 2 molded into a predetermined shape, 750 to 1100 ° C. The molded product that is molded by the molding step, preferably 850 to
And a sintering step of sintering by heating at a temperature of 1000 ° C., thereby having an effect of stabilizing the capacitance value of the carbon dioxide gas sensor.
【0021】本発明の請求項5に記載の炭酸ガスセンサ
は、請求項1乃至3の内いずれか1に記載の炭酸ガスセ
ンサ用無機組成物を用い請求項4の製造方法で形成され
た炭酸ガス検知部と、炭酸ガス検知部上に配設された電
気信号取り出し用の電極と、を備えたこととしたもので
あり、これにより検知感度が高く、検知特性のばらつき
が少ない炭酸ガスセンサが得られるという作用を有す
る。A carbon dioxide sensor according to a fifth aspect of the present invention uses the inorganic composition for a carbon dioxide sensor according to any one of the first to third aspects to detect a carbon dioxide gas formed by the method according to the fourth aspect. And an electrode for extracting an electric signal disposed on the carbon dioxide gas detecting section, whereby a carbon dioxide gas sensor having high detection sensitivity and little variation in detection characteristics can be obtained. Has an action.
【0022】以下に、本発明の実施の形態の具体例を図
面を参照しながら説明する。ここに、CeO2、BaC
O3、CuOを含有する炭酸ガスセンサ用無機組成物で
あって、CeO2、BaCO3、CuOのモル比を、Ce
O2=A、BaCO3=B、CuO=Cとし、A+B+C
=100モル%としたときに、Aのモル%が45≦A≦
95、好ましくは50≦A≦90の範囲にある炭酸ガス
センサ用無機組成物である。以上のように構成された炭
酸ガスセンサの製造方法を以下に説明する。Hereinafter, specific examples of the embodiments of the present invention will be described with reference to the drawings. Here, CeO 2 , BaC
An inorganic composition for a carbon dioxide gas sensor containing O 3 and CuO, wherein the molar ratio of CeO 2 , BaCO 3 , and CuO is Ce
O 2 = A, BaCO 3 = B, CuO = C, A + B + C
= 100 mol%, the mol% of A is 45 ≦ A ≦
95, preferably an inorganic composition for a carbon dioxide sensor in the range of 50 ≦ A ≦ 90. A method for manufacturing the carbon dioxide sensor configured as described above will be described below.
【0023】まず、混合粉砕工程として、所定の組成比
で秤量されたCeO2、BaCO3、CuOをボールミル
等を用いて湿式混合、粉砕し、乾燥機等を用いて乾燥さ
せ、混合粉末を得る。First, in a mixing and pulverizing step, CeO 2 , BaCO 3 , and CuO weighed at a predetermined composition ratio are wet-mixed using a ball mill or the like, pulverized, and dried using a drier or the like to obtain a mixed powder. .
【0024】次に成型工程として、混合粉砕工程により
得られた混合粉末を板状や櫛形等の所定の形状に0.5
〜2t/cm2範囲の圧力で成型する。Next, as a molding step, the mixed powder obtained in the mixing and pulverizing step is formed into a predetermined shape such as a plate shape or a comb shape by 0.5 mm.
Mold at a pressure in the range of 22 t / cm 2 .
【0025】次に焼成工程として、成型工程で成型され
た成型物を850〜1000℃の温度で加熱して焼結す
ることにより炭酸ガスセンサの検知部が得られる。Next, as a firing step, the molded part molded in the molding step is heated at a temperature of 850 to 1000 ° C. and sintered to obtain a detecting portion of the carbon dioxide gas sensor.
【0026】この炭酸ガス検知部上に公知の方法により
少なくとも2つの電極を形成することによって炭酸ガス
センサが得られる。A carbon dioxide sensor can be obtained by forming at least two electrodes on the carbon dioxide detecting section by a known method.
【0027】以上のように本実施の形態によれば、炭酸
ガスの検知感度が高く、検知速度が速く静電容量値の安
定した炭酸ガスセンサ用無機組成物を作製するための原
料粉末を得ることができる。As described above, according to the present embodiment, it is possible to obtain a raw material powder for producing an inorganic composition for a carbon dioxide gas sensor having a high carbon dioxide gas detection sensitivity, a high detection speed, and a stable capacitance value. Can be.
【0028】また、この原料粉末を成型、焼成すること
により炭酸ガスの検知感度が高く、かつ検知速度の速い
炭酸ガスセンサ用無機組成物からなる炭酸ガス検知部を
簡便に作製できるとともに、高品質かつ安定した品質で
低原価で量産することができる。By molding and firing the raw material powder, it is possible to easily produce a carbon dioxide gas detecting portion made of an inorganic composition for a carbon dioxide gas sensor having a high carbon dioxide gas detection sensitivity and a high detection speed, and to obtain a high quality carbon dioxide gas. It can be mass-produced at low cost with stable quality.
【0029】(実施の形態1)図1は本発明の第1実施
の形態における炭酸ガスセンサの断面図である。(Embodiment 1) FIG. 1 is a sectional view of a carbon dioxide sensor according to a first embodiment of the present invention.
【0030】図1において、1は炭酸ガスセンサ用無機
組成物からなる炭酸ガス検知部、2a、2bは電極、3
a、3bはリード線である。In FIG. 1, reference numeral 1 denotes a carbon dioxide gas detecting portion made of an inorganic composition for a carbon dioxide gas sensor, 2a and 2b denote electrodes,
a and 3b are lead wires.
【0031】本実施の形態における炭酸ガスセンサは、
炭酸ガス検知部1と、炭酸ガス検知部1上に配設された
電気信号取り出し用の電極2a、2bと、電気信号取り
出し用の電極2a、2b上に配設されたリード線3a、
3bと、を備えている。The carbon dioxide sensor according to the present embodiment is
A carbon dioxide gas detecting section 1, electrodes 2a and 2b for extracting electric signals provided on the carbon dioxide detecting section 1, and lead wires 3a provided on the electrodes 2a and 2b for extracting electric signals;
3b.
【0032】ここで、炭酸ガス検知部1原料の酸化物及
び炭酸塩を所定の組成で、湿式混合、粉砕し、原料粒径
が0.1μm以上2μm以下の粒子で構成された混合粉
末を成型、焼成して得られる焼結体で構成されているこ
とである。Here, the oxides and carbonates of the raw material of the carbon dioxide gas detection unit 1 are wet-mixed and pulverized in a predetermined composition to form a mixed powder composed of particles having a raw material particle size of 0.1 μm or more and 2 μm or less. And a sintered body obtained by firing.
【0033】本実施の形態における炭酸ガスセンサは、
第1実施の形態における炭酸ガスセン用無機組成物の製
造方法により得られる。また、電極2a、2bは動作温
度で変質せず抵抗の小さい材料であればよく、Au、P
t、RuO2、Ag等のいずれかを含有するペーストを
スクリーン印刷した後、熱処理する方法等により形成す
ることができる。なお、リード線3a、3bとしては板
状または線状等のPt、Ni、Au等が用いられる。The carbon dioxide sensor in the present embodiment is
It can be obtained by the method for producing an inorganic composition for carbon dioxide gas in the first embodiment. The electrodes 2a and 2b may be made of any material that does not deteriorate at the operating temperature and has a small resistance.
The paste can be formed by screen printing a paste containing any of t, RuO 2 , Ag and the like, followed by heat treatment. In addition, Pt, Ni, Au or the like in a plate shape or a linear shape is used as the lead wires 3a and 3b.
【0034】上記構成を有する炭酸ガスセンサを用いて
炭酸ガス濃度を検知する方法は従来例と同様であり、例
えば電気炉内等に本実施の形態における炭酸ガスセンサ
を設置し、炭酸ガス濃度を測定しようとする被検ガスを
通気しながら、リード線3a、3b間の静電容量の電気
的特性を測定することにより検知することができる。The method of detecting the concentration of carbon dioxide using the carbon dioxide sensor having the above configuration is the same as that of the conventional example. For example, the carbon dioxide sensor according to the present embodiment is installed in an electric furnace or the like to measure the carbon dioxide concentration. Can be detected by measuring the electrical characteristics of the capacitance between the lead wires 3a and 3b while passing the test gas.
【0035】以上のように本実施の形態によれば、炭酸
ガスの検知感度が高く、検知速度が早く、かつ静電容量
値の安定した炭酸ガスセンサを提供することができる。As described above, according to the present embodiment, it is possible to provide a carbon dioxide gas sensor having a high carbon dioxide gas detection sensitivity, a high detection speed, and a stable capacitance value.
【0036】[0036]
【実施例】以下に、本発明を第1実施の形態を実施例1
〜15及び比較例1〜10を用いて詳細に説明する。DESCRIPTION OF THE PREFERRED EMBODIMENTS The first embodiment of the present invention will be described below with reference to the first embodiment.
This will be described in detail with reference to Comparative Examples 1 to 10.
【0037】(実施例1〜15、比較例1〜10)市販
分析級純度の炭酸バリウム、酸化セリウム、酸化銅を
(表1)の組成比で全量が100gとなるように各々秤
量した後容器に移し、エタノール80mlを加え、ボー
ルミルを用いて混合粉砕し、乾燥機を用いて80〜13
0℃で乾燥して得られた混合粉末を、プレス機を用いて
0.5t/cm2の圧力で直径20mm、厚み0.5m
mの大きさのディスク状に成型した。得られた成型体を
電気炉中で850℃で5時間焼成した。焼成した試料の
両面に市販分析級純度の酸化ルテニウムペーストを円形
に塗布し、900℃で10分間熱処理して電極部を作製
した。この試料を切断機を用いて、1.6mm×1.1
5mm×0.5mmの大きさに切断し、酸化ルテニウム
電極両面に市販分析級純度の酸化ルテニウムペーストを
用いて白金線をつけてリード線とし、850℃で10分
間熱処理した。(Examples 1 to 15 and Comparative Examples 1 to 10) Barium carbonate, cerium oxide and copper oxide of analytical grade purity were weighed so that the total amount was 100 g in the composition ratio of (Table 1), and then the container was prepared. The mixture was added to 80 ml of ethanol, mixed and pulverized using a ball mill, and dried at 80 to 13 using a drier.
The mixed powder obtained by drying at 0 ° C. was pressed with a press machine at a pressure of 0.5 t / cm 2 at a diameter of 20 mm and a thickness of 0.5 m.
m was molded into a disk shape. The obtained molded body was fired in an electric furnace at 850 ° C. for 5 hours. A commercially available ruthenium oxide paste of analytical grade purity was applied in a circular shape on both surfaces of the fired sample, and heat-treated at 900 ° C. for 10 minutes to produce an electrode portion. Using a cutting machine, this sample was 1.6 mm × 1.1.
It was cut into a size of 5 mm × 0.5 mm, and a platinum wire was attached to both surfaces of the ruthenium oxide electrode using a commercially available ruthenium oxide paste of analytical grade purity to form a lead wire, which was then heat-treated at 850 ° C. for 10 minutes.
【0038】以上のように作製した炭酸ガスセンサを第
1〜15実施例、第1〜10比較例とした。The carbon dioxide sensors manufactured as described above were referred to as first to fifteenth examples and first to tenth comparative examples.
【0039】(比較例11)第1実施例と同様にして、
市販分析級純度の炭酸バリウム、酸化セリウム、酸化銅
を70:10:20の組成比で全量が100gとなるよ
うに各々秤量した後容器に移し、ボールミルを用いて混
合粉砕し、得られた混合粉末を、プレス機を用いて0.
5t/cm2の圧力で直径20mm、厚み0.5mmの
大きさのディスク状に成型した。得られた成型体を電気
炉中で850℃で5時間焼成した。この焼結体に第1実
施例と同様に電極を形成し、切断を行い、リード線を形
成した。(Comparative Example 11) As in the first embodiment,
Barium carbonate, cerium oxide, and copper oxide having a commercial analytical purity were weighed at a composition ratio of 70:10:20 so that the total amount was 100 g, then transferred to a container, mixed and pulverized using a ball mill, and the resulting mixture was obtained. The powder was placed in a 0.
It was molded into a disk having a diameter of 20 mm and a thickness of 0.5 mm under a pressure of 5 t / cm 2 . The obtained molded body was fired in an electric furnace at 850 ° C. for 5 hours. An electrode was formed on this sintered body in the same manner as in the first embodiment, cut, and a lead wire was formed.
【0040】以上のようにして作製した炭酸ガスセンサ
を第11比較例とした。 (評価例1)第1〜15実施例、第1〜5比較例におけ
る炭酸ガスセンサの性能を比較するために、以下のよう
な炭酸ガス濃度に対する感度試験を行った。The carbon dioxide sensor manufactured as described above was used as an eleventh comparative example. (Evaluation Example 1) In order to compare the performances of the carbon dioxide gas sensors in the first to fifteenth examples and the first to fifth comparative examples, the following sensitivity tests were performed on the carbon dioxide concentration.
【0041】各炭酸ガスセンサを、550℃に調整され
た電気炉中に配置し、電気炉内に乾燥空気を通気した状
態と2%の炭酸ガスを含む乾燥空気を通気した状態で、
各々インピーダンスアナライザ(YHP社製、4192
A型)を用いて2端子法で周波数10kHzにおけるリ
ード線間の静電容量成分を測定した。なお、静電容量成
分、乾燥空気または2%の炭酸ガスを含む乾燥空気を電
気炉内に通気してからほぼ一定値となるまで行い、一定
値となったところで静電容量成分を決定した。Each of the carbon dioxide sensors was placed in an electric furnace adjusted to 550 ° C., and dried air was passed through the electric furnace and dry air containing 2% carbon dioxide was passed through the electric furnace.
Each impedance analyzer (4192, manufactured by YHP)
(A type), the capacitance component between the lead wires at a frequency of 10 kHz was measured by a two-terminal method. The capacitance component, dry air or dry air containing 2% carbon dioxide gas was passed through the electric furnace until the value reached a substantially constant value, and the capacitance component was determined when the value reached the constant value.
【0042】炭酸ガスの検知状況は、測定温度まで加熱
された試料の、空気を流入した状態で測定した静電容量
値(Cair)を基準とし、炭酸ガス濃度2%に調整され
た空気入させて測定したときの静電容量値(C2%)の変
化でとらえられる。感度は次式で定義する。The detection state of the carbon dioxide gas is based on the capacitance value (C air ) of the sample heated to the measurement temperature measured in a state where the air is introduced, and the air inlet adjusted to the carbon dioxide gas concentration of 2%. It is captured by the change in the capacitance value (C 2% ) when the measurement is performed. The sensitivity is defined by the following equation.
【0043】 感度=|10×Log(C2%/Cair)| [dB] 数値が大きい方が感度がよい。感度が0の時は静電容量
値が炭酸ガス濃度の増加に対し変化を示していないこと
をあらわし、炭酸ガスを検知しないことになる。実施例
1〜15、比較例1〜5の感度特性10を(表1)に示
した。Sensitivity = | 10 × Log (C 2% / C air ) | [dB] The larger the numerical value, the better the sensitivity. When the sensitivity is 0, it indicates that the capacitance value does not show a change with respect to an increase in the concentration of carbon dioxide, and no carbon dioxide is detected. The sensitivity characteristics 10 of Examples 1 to 15 and Comparative Examples 1 to 5 are shown in (Table 1).
【0044】[0044]
【表1】 [Table 1]
【0045】(表1)から明らかなように、本実施例に
おいては感度が5dB以上であり、その際にCeO2の
組成比が50〜90の範囲にあることが判明した。As is clear from Table 1, in this example, the sensitivity was 5 dB or more, and at that time, the composition ratio of CeO 2 was found to be in the range of 50 to 90.
【0046】これは、炭酸ガスセンサ用無機組成物にお
いて触媒的作用を有する酸化セリウムの特性がこの範囲
において最も有効に作用していることが、検知感度が高
くなっている要因の1つとして考えられる。It is considered that one of the reasons for the high detection sensitivity is that the characteristic of cerium oxide having a catalytic action in the inorganic composition for a carbon dioxide sensor works most effectively in this range. .
【0047】(評価例2)第5〜8及び第11実施例と
第6〜10比較例における炭酸ガスセンサの性能を比較
するために各々100個作製し、(評価例1)と同様に
測定し、感度特性の平均値及び測定した感度特性から各
々の標準偏差を算出した、感度ばらつきの範囲を(表
2)に示した。また、第5〜8及び第11実施例、第6
〜10比較例の炭酸ガスセンサの検知速度を比較するた
めに、炭酸ガス濃度を変えたとき、その特性変化量が全
変化量の90%となるに要した時間を”90%検知時
間”として(表2)に示した。(Evaluation Example 2) In order to compare the performances of the carbon dioxide gas sensors in the fifth to eighth and eleventh embodiments and the sixth to tenth comparative examples, 100 sensors were manufactured and measured in the same manner as in (Evaluation Example 1). The average value of the sensitivity characteristics and the standard deviation of each were calculated from the measured sensitivity characteristics, and the range of sensitivity variation is shown in Table 2. In addition, the fifth to eighth and eleventh embodiments and the sixth embodiment
In order to compare the detection speeds of the carbon dioxide gas sensors of Comparative Examples 10 to 10, when the carbon dioxide gas concentration was changed, the time required for the characteristic change amount to become 90% of the total change amount was defined as "90% detection time" ( The results are shown in Table 2).
【0048】[0048]
【表2】 [Table 2]
【0049】(表2)から明らかなように、本実施例の
ように炭酸ガスセンサ用無機組成物の組成において1.
5B≦C≦2.5Bの範囲では、検知感度も5dB以上
で感度のばらつきも小さくなっているが、この範囲を超
えると検知感度の低下やばらつきの増加が起こることが
明らかとなった。As is clear from Table 2, in the composition of the inorganic composition for a carbon dioxide gas sensor as in this example, 1.
In the range of 5B ≦ C ≦ 2.5B, the variation in sensitivity is small when the detection sensitivity is 5 dB or more. However, it is clear that the detection sensitivity is reduced and the variation is increased when the sensitivity exceeds this range.
【0050】また、90%検知時間についても同様であ
ることが判明した。これは、C<1.5Bにおいては、
炭酸バリウムの過多による検知機構の鈍化が要因として
考えられる。またC>2.5Bにおいては、炭酸バリウ
ムの過小による検知感度の低下及び酸化銅の過多による
炭酸ガスセンサ用無機組成物の低抵抗化が特性を不安定
にしていることが要因として考えられる。It was also found that the same applies to the 90% detection time. This is, for C <1.5B,
It is considered that the detection mechanism is slowed down due to excessive barium carbonate. When C> 2.5B, it is considered that the detection sensitivity is lowered due to an excessively small amount of barium carbonate, and the resistance of the inorganic composition for a carbon dioxide gas sensor is decreased due to an excessive amount of copper oxide, which makes the characteristics unstable.
【0051】(評価例3)第5実施例及び第11比較例
の炭酸ガスセンサを各々100個作製し、(評価例1)
と同様にして空気中における静電容量値を測定した。ま
た、それぞれの原料粉末の粒度を粒度分布測定装置(H
ORIBA社製LA−700型、レーザ回折/散乱式粒
度分布測定装置)を用いて測定した。測定した静電容量
値から各々の標準偏差を算出し、静電容量値のばらつき
の範囲及び原料の粒度分布を(表3)にまとめた。(Evaluation Example 3) 100 carbon dioxide sensors of the fifth embodiment and the eleventh comparative example were manufactured, respectively (Evaluation Example 1).
The capacitance value in air was measured in the same manner as described above. In addition, the particle size of each raw material powder is measured using a particle size distribution analyzer (H
The laser diffraction / scattering type particle size distribution measuring apparatus (LA-700, manufactured by ORIBA) was used. The respective standard deviations were calculated from the measured capacitance values, and the range of variation of the capacitance values and the particle size distribution of the raw materials were summarized in (Table 3).
【0052】[0052]
【表3】 [Table 3]
【0053】(表3)から明らかなように、乾式混合を
行った第11比較例が、静電容量値の分布範囲が30%
を越えているのに比べて、湿式混合を行った第5実施例
は、8.3%とその範囲が小さくなっていることが明ら
かとなった。また、原料の粒度分布も第11比較例が
1.8〜12μmと広範囲にわたっているのに比べて、
第1実施例では、0.1〜2μmの粒子で構成されてい
ることが明らかとなった。これは、湿式混合を行うこと
で原料の粉砕が均一に行われるとともに、粒子が小さく
なることで原料中の組成分布が非常に均質になるため
に、焼結体の特性が安定すると考えられる。また、炭酸
ガスの拡散についても、炭酸ガス検知部内の粒界が均一
であるために、拡散速度が速く一定となるので、検知感
度が高くなっている要因の一つであると考えられる。As apparent from Table 3, the eleventh comparative example in which the dry mixing was performed showed that the capacitance value distribution range was 30%.
In the fifth embodiment in which the wet mixing was performed, the range was 8.3%, which was smaller than that in the case where the ratio exceeded 8.3%. In addition, the particle size distribution of the raw material is also wide in the eleventh comparative example as 1.8 to 12 μm,
In the first example, it was clarified that the particles were composed of 0.1 to 2 μm particles. This is considered to be because the properties of the sintered body are stabilized because the raw material is uniformly pulverized by performing the wet mixing, and the composition distribution in the raw material becomes very uniform due to the small particles. The diffusion of carbon dioxide gas is also considered to be one of the factors that increase the detection sensitivity because the diffusion speed is high and constant because the grain boundaries in the carbon dioxide gas detection unit are uniform.
【0054】また、第5実施例及び第11比較例につい
て、より実用的な炭酸ガス濃度領域について感度特性を
測定した。炭酸ガス濃度は、Air〜5000ppmと
した。The sensitivity characteristics of the fifth embodiment and the eleventh comparative example were measured in a more practical carbon dioxide gas concentration region. The carbon dioxide gas concentration was set to Air to 5000 ppm.
【0055】第5実施例及び第11比較例のAir〜5
000ppmにおける感度特性を(図2)に示した。Air to 5 of the fifth embodiment and the eleventh comparative example
The sensitivity characteristics at 000 ppm are shown in FIG.
【0056】(図2)から明らかなように、乾式混合を
行った第11比較例では500〜3000ppmの濃度
域における感度が低くなっているのに対し、湿式混合を
行った第5実施例では2倍程度の感度を示すことが判明
した。As apparent from FIG. 2, the sensitivity in the concentration range of 500 to 3000 ppm is low in the eleventh comparative example in which the dry mixing is performed, whereas the sensitivity in the concentration range of 500 to 3000 ppm is low in the fifth embodiment in which the wet mixing is performed. It turned out that it shows about twice the sensitivity.
【0057】このことも原料の粒子が小さくなったこと
で、炭酸ガスの検知部の有効表面積が従来より大きく存
在しているために、炭酸ガスが低濃度の場合においても
高い感度を示すと考えられる。This is also considered to be due to the fact that the effective particle surface area of the carbon dioxide gas detection part is larger than in the prior art due to the reduced particle size of the raw material, so that high sensitivity is exhibited even when the carbon dioxide gas concentration is low. Can be
【0058】(評価例4)第5実施例と第1及び第11
比較例の炭酸ガスセンサを各々、85℃90%Rhに調
整された恒温恒湿器に1000時間放置した後、(評価
例1)と同様にして炭酸ガスの検知感度を決定した。こ
れらの値を(表4)にまとめた。(Evaluation Example 4) Fifth Embodiment and First and Eleventh Embodiments
After leaving each of the carbon dioxide sensors of the comparative examples in a thermo-hygrostat adjusted to 85 ° C. and 90% Rh for 1000 hours, the detection sensitivity of the carbon dioxide gas was determined in the same manner as in (Evaluation Example 1). These values are summarized in (Table 4).
【0059】その結果、第1及び第11比較例の炭酸ガ
スセンサでは1000時間放置する前に比べて検知感度
が18.4%及び16.3%低下するのに対して、第5
実施例の炭酸ガスセンサでは検知感度の低下は5.1%
と極めて小さく、本発明の炭酸ガスセンサは耐湿性につ
いても従来例に比べて向上されることが判明した。As a result, in the carbon dioxide gas sensors of the first and eleventh comparative examples, the detection sensitivity was reduced by 18.4% and 16.3% as compared with that before leaving for 1000 hours.
In the carbon dioxide gas sensor of the embodiment, the decrease in the detection sensitivity is 5.1%.
It was found that the carbon dioxide sensor of the present invention was improved in moisture resistance as compared with the conventional example.
【0060】(評価例5)第5実施例と第1及び第11
比較例の炭酸ガスセンサを各々、550℃に調整された
電気炉内に1000時間放置した後、(評価例1)と同
様にして炭酸ガスの検知感度を決定した。(Evaluation Example 5) Fifth Embodiment and First and Eleventh Embodiments
After leaving each of the carbon dioxide sensors of the comparative examples in an electric furnace adjusted to 550 ° C. for 1000 hours, the detection sensitivity of carbon dioxide was determined in the same manner as in (Evaluation Example 1).
【0061】これらの値を(表4)にまとめた。These values are summarized in (Table 4).
【0062】[0062]
【表4】 [Table 4]
【0063】その結果、第1及び第11比較例の炭酸ガ
スセンサでは1000時間放置する前に比べて検知感度
が13.4%及び10.6%低下するのに対して、第5
実施例の炭酸ガスセンサでは検知感度の低下は2.9%
と極めて小さく、本発明の炭酸ガスセンサは、耐久性、
寿命特性についても従来例に比べて向上されることが判
明した。As a result, in the carbon dioxide gas sensors of the first and eleventh comparative examples, the detection sensitivity was reduced by 13.4% and 10.6% as compared with that before leaving for 1000 hours.
In the carbon dioxide sensor of the embodiment, the decrease in the detection sensitivity is 2.9%.
And extremely small, the carbon dioxide sensor of the present invention is durable,
It was also found that the life characteristics were improved as compared with the conventional example.
【0064】このように(評価例4)の耐湿性、(評価
例5)の耐久性、寿命特性の向上には、反応性が均質な
粒子で構成されているために炭酸ガス検知部にクラック
が少なく、水分や熱の影響を受けにくくなっていること
や粒子状態が一定であるために、炭酸ガス検知部と電極
との密着性が良くなっていること等によるものと考えら
れる。As described above, in order to improve the moisture resistance of (Evaluation Example 4), the durability and the life characteristics of (Evaluation Example 5), cracks are formed in the carbon dioxide gas detecting portion because the particles are composed of particles having uniform reactivity. This is considered to be due to the fact that the adhesiveness between the carbon dioxide gas detecting portion and the electrode is improved due to the fact that the carbon dioxide gas is less affected by moisture and heat and the particle state is constant.
【0065】[0065]
【発明の効果】以上のように本発明においては、以下の
優れた効果を実現できる。As described above, according to the present invention, the following excellent effects can be realized.
【0066】本発明の請求項1の炭酸ガスセンサ用無機
組成物によれば、炭酸ガスの検知感度が高く、静電容量
値の安定した炭酸ガスセンサを与えるとともに、高品質
かつ安定した品質で低原価で量産できる炭酸ガスセンサ
用無機組成物を実現することができる。According to the inorganic composition for a carbon dioxide sensor of the first aspect of the present invention, a carbon dioxide gas sensor having high sensitivity for detecting carbon dioxide and having a stable capacitance value is provided, and high quality, stable quality and low cost are provided. Thus, an inorganic composition for a carbon dioxide gas sensor that can be mass-produced can be realized.
【0067】本発明の請求項2に記載の炭酸ガスセンサ
用無機組成物によれば、請求項1の発明で得られる効果
に加え、炭酸ガスの検知感度を向上させ、特に感度特性
を安定にすることができるという効果が得られる。According to the inorganic composition for a carbon dioxide sensor according to the second aspect of the present invention, in addition to the effects obtained by the first aspect, the detection sensitivity of the carbon dioxide gas is improved, and particularly the sensitivity characteristics are stabilized. The effect that it can be obtained is obtained.
【0068】本発明の請求項3に記載の炭酸ガスセンサ
用無機組成物によれば、本発明の請求項1または2の内
のいずれか1に記載の発明に加え、粒子の凝集を防止で
きるとともに、検知特性のばらつきを抑制することがで
きるという効果が得られる。According to the inorganic composition for a carbon dioxide sensor of the third aspect of the present invention, in addition to the invention of any one of the first and second aspects of the present invention, aggregation of particles can be prevented. In addition, the effect of suppressing variations in detection characteristics can be obtained.
【0069】本発明の請求項4に記載の炭酸ガスセンサ
用無機組成物の製造方法によれば、炭酸ガスの検知感度
が高く、高品質かつ安定した品質で量産性に優れた炭酸
ガスセンサを効率よく生産できる炭酸ガスセンサの製造
方法を実現できる。According to the method for producing an inorganic composition for a carbon dioxide gas sensor according to the fourth aspect of the present invention, a carbon dioxide gas sensor having high sensitivity for detecting carbon dioxide, high quality, stable quality and excellent mass productivity can be efficiently produced. A method of manufacturing a carbon dioxide sensor that can be produced can be realized.
【0070】本発明の請求項5に記載の炭酸ガスセンサ
によれば、炭酸ガス検知部を構成する無機組成物の分布
が均一であることにより、検知特性のばらつきが少ない
信頼性の高い炭酸ガスセンサを提供することができると
ともに、炭酸ガスセンサの信頼性を向上させることがで
きるという優れた効果が得られる。According to the carbon dioxide sensor according to the fifth aspect of the present invention, since the distribution of the inorganic composition constituting the carbon dioxide sensing portion is uniform, a highly reliable carbon dioxide sensor having little variation in detection characteristics is provided. An excellent effect of being able to provide and improving the reliability of the carbon dioxide sensor is obtained.
【図1】本発明の第1実施の形態における炭酸ガスセン
サの断面図FIG. 1 is a sectional view of a carbon dioxide sensor according to a first embodiment of the present invention.
【図2】本発明の第3評価例における特性比較図FIG. 2 is a characteristic comparison diagram in a third evaluation example of the present invention.
1 炭酸ガス検知部 2a,2b 電極 3a,3b リード線 1 Carbon dioxide detector 2a, 2b Electrode 3a, 3b Lead wire
Claims (5)
酸ガスセンサ用無機組成物であって、CeO2、BaC
O3、CuOのモル比を、CeO2=A、BaCO3=
B、CuO=Cとし、A+B+C=100モル%とした
ときに、Aのモル%が45≦A≦95、好ましくは50
≦A≦90の範囲にあることを特徴とする炭酸ガスセン
サ用無機組成物。An inorganic composition for a carbon dioxide sensor containing CeO 2 , BaCO 3 , and CuO, wherein the inorganic composition is CeO 2 , BaC
The molar ratios of O 3 and CuO are expressed as CeO 2 = A, BaCO 3 =
B, when CuO = C and A + B + C = 100 mol%, the mol% of A is 45 ≦ A ≦ 95, preferably 50
An inorganic composition for a carbon dioxide gas sensor, wherein satisfies the range of ≦ A ≦ 90.
Bに対し1.5B≦C≦2.5Bの範囲にあることを特
徴とする請求項1に記載の炭酸ガスセンサ用無機組成
物。2. The inorganic composition for a carbon dioxide sensor according to claim 1, wherein, in the molar ratio B + C, the molar percentage of C is in the range of 1.5B ≦ C ≦ 2.5B with respect to B.
る炭酸ガスセンサ用無機組成物の原料粉末の粒径が0.
1ミクロン以上2ミクロン以下であることを特徴とする
請求項1または2の内のいずれか1に記載の炭酸ガスセ
ンサ用無機組成物。3. The raw material powder of the inorganic composition for a carbon dioxide gas sensor containing CeO 2 , BaCO 3 , and CuO has a particle size of 0.1.
The inorganic composition for a carbon dioxide sensor according to any one of claims 1 and 2, wherein the inorganic composition is at least 1 micron and at most 2 microns.
酸ガスセンサ用無機組成物を0.3〜2.5t/c
m2、好ましくは0.5〜2t/cm2の圧力で所定の形
状に成型する成型工程と、前記成型工程で成型された成
型物を750〜1100℃、好ましくは850〜100
0℃の温度で加熱して焼結する焼成工程と、を備えたこ
とを特徴とする炭酸ガスセンサの製造方法。4. An inorganic composition for a carbon dioxide sensor according to claim 1, wherein said inorganic composition is 0.3 to 2.5 t / c.
m 2 , preferably a molding step of molding into a predetermined shape at a pressure of 0.5 to 2 t / cm 2 , and a molded article molded in the molding step is 750 to 1100 ° C., preferably 850 to 100 ° C.
A firing step of sintering by heating at a temperature of 0 ° C.
酸ガスセンサ用無機組成物を用い請求項4の製造方法で
形成された炭酸ガス検知部と、前記炭酸ガス検知部に配
設された電気信号取り出し用の電極と、を備えたことを
特徴とする炭酸ガスセンサ。5. A carbon dioxide gas detecting section formed by the method according to claim 4 using the carbon dioxide sensor inorganic composition according to any one of claims 1 to 3, and provided in the carbon dioxide gas detecting section. And an electrode for extracting an electric signal.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12570798A JPH11326259A (en) | 1998-05-08 | 1998-05-08 | Inorganic composition for carbon dioxide sensor, manufacture of carbon dioxide sensor and carbon dioxide sensor obtained by it |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12570798A JPH11326259A (en) | 1998-05-08 | 1998-05-08 | Inorganic composition for carbon dioxide sensor, manufacture of carbon dioxide sensor and carbon dioxide sensor obtained by it |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH11326259A true JPH11326259A (en) | 1999-11-26 |
Family
ID=14916750
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12570798A Pending JPH11326259A (en) | 1998-05-08 | 1998-05-08 | Inorganic composition for carbon dioxide sensor, manufacture of carbon dioxide sensor and carbon dioxide sensor obtained by it |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH11326259A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2021124405A (en) * | 2020-02-06 | 2021-08-30 | アズビル株式会社 | CO2 sensor system |
-
1998
- 1998-05-08 JP JP12570798A patent/JPH11326259A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2021124405A (en) * | 2020-02-06 | 2021-08-30 | アズビル株式会社 | CO2 sensor system |
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