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JP3301144B2 - Carbon monoxide detector - Google Patents
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JP3301144B2 - Carbon monoxide detector - Google Patents

Carbon monoxide detector

Info

Publication number
JP3301144B2
JP3301144B2 JP04354893A JP4354893A JP3301144B2 JP 3301144 B2 JP3301144 B2 JP 3301144B2 JP 04354893 A JP04354893 A JP 04354893A JP 4354893 A JP4354893 A JP 4354893A JP 3301144 B2 JP3301144 B2 JP 3301144B2
Authority
JP
Japan
Prior art keywords
carbon monoxide
concentration
piezoelectric substrate
metal composite
composite oxide
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 - Fee Related
Application number
JP04354893A
Other languages
Japanese (ja)
Other versions
JPH06258210A (en
Inventor
孝裕 梅田
彪 長井
邦弘 鶴田
謙三 黄地
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.)
Panasonic Corp
Panasonic Holdings Corp
Original Assignee
Panasonic Corp
Matsushita Electric Industrial 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 Panasonic Corp, Matsushita Electric Industrial Co Ltd filed Critical Panasonic Corp
Priority to JP04354893A priority Critical patent/JP3301144B2/en
Publication of JPH06258210A publication Critical patent/JPH06258210A/en
Application granted granted Critical
Publication of JP3301144B2 publication Critical patent/JP3301144B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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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 Ultrasonic Waves (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、例えばボンベに充填し
たCOの濃度を酸素共存下においても検知することので
きる一酸化炭素検出素子に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a carbon monoxide detecting element capable of detecting the concentration of CO charged in a cylinder, for example, even in the presence of oxygen.

【0002】[0002]

【従来の技術】従来より、COを検出定量する一酸化炭
素検出素子が提案されている。例えば、酸化錫(SnO
2)薄膜を用いた一酸化炭素検出素子は前記SnO2薄膜
によりCOを吸着し、前記SnO2薄膜の電気抵抗値の
変化を利用してCOの濃度を検出できる。
2. Description of the Related Art Hitherto, a carbon monoxide detecting element for detecting and quantifying CO has been proposed. For example, tin oxide (SnO)
2) carbon monoxide detector element using a thin film can detect the SnO 2 adsorbed CO by thin, the concentration of CO by using a change of the SnO 2 thin film resistivity.

【0003】また、一般に酸素欠陥構造あるいはペロブ
スカイト型構造を有する金属複合酸化物がCOを吸着お
よび吸収することが知られている。
It is generally known that a metal composite oxide having an oxygen deficiency structure or a perovskite structure adsorbs and absorbs CO.

【0004】[0004]

【発明が解決しようとする課題】しかしながら従来の技
術では、選択的にCOを検出することができず、雰囲気
中に酸素(O2)が存在する場合、O2も吸着してしまう
ため正確なCOの濃度が得られないという課題があっ
た。
However, in the prior art, CO cannot be selectively detected, and when oxygen (O 2 ) is present in the atmosphere, O 2 is also adsorbed. There was a problem that the concentration of CO could not be obtained.

【0005】本発明は上記課題を解決するもので、雰囲
気中にO2が存在しても選択的にCOを検出することが
できる一酸化炭素検出素子を提供することを目的とした
ものである。
An object of the present invention is to solve the above-mentioned problems, and an object of the present invention is to provide a carbon monoxide detecting element capable of selectively detecting CO even when O 2 is present in an atmosphere. .

【0006】[0006]

【課題を解決するための手段】上記目的を達成するため
に本発明は、圧電基板と、前記圧電基板上に形成された
弾性波を励振するための電極と、弾性波伝播路上に配置
されたCOを選択的に吸着および吸収する金属複合酸化
物とから成るものである。
In order to achieve the above object, the present invention provides a piezoelectric substrate, an electrode for exciting an elastic wave formed on the piezoelectric substrate, and an electrode disposed on an elastic wave propagation path. And a metal composite oxide that selectively adsorbs and absorbs CO.

【0007】[0007]

【作用】本発明は上記構成によって、圧電基板上に酸素
共存下でCOを選択的に吸着および吸収する金属複合酸
化物を薄膜で形成し、前記金属複合酸化物にCOを吸着
および吸収させる。さらに電極に高周波を印加すること
により前記圧電基板表面に弾性波を励振させる。そして
周波数の変化よりCOの濃度を検出することができる。
According to the present invention, a metal composite oxide capable of selectively adsorbing and absorbing CO in the coexistence of oxygen is formed in a thin film on the piezoelectric substrate, and the CO is adsorbed and absorbed by the metal composite oxide. Further, an elastic wave is excited on the surface of the piezoelectric substrate by applying a high frequency to the electrode. Then, the CO concentration can be detected from the change in the frequency.

【0008】[0008]

【実施例】以下本発明の一実施例について、図面を参照
しながら説明する。図1において、ニオブ酸リチウムに
より厚さ0.5mm程度の矩形状に形成した圧電基板1の
一方の表面の両端部に、弾性波を励振するための一対の
櫛形電極2、3を金により形成した。さらに酸素欠陥構
造を持つ金属複合酸化物4としてイットリウムバリウム
銅酸化物(YBa2Cu37 )を反応性高周波マグネト
ロンスパッタリング法により圧電基板1の弾性波伝播路
上に形成した。膜厚は約5000Åであった。
An embodiment of the present invention will be described below with reference to the drawings. In FIG. 1, a pair of comb-shaped electrodes 2 and 3 for exciting elastic waves are formed of gold on both ends of one surface of a piezoelectric substrate 1 formed of lithium niobate into a rectangular shape having a thickness of about 0.5 mm. did. Further, yttrium barium copper oxide (YBa 2 Cu 3 O 7 ) was formed on the elastic wave propagation path of the piezoelectric substrate 1 by a reactive high-frequency magnetron sputtering method as the metal composite oxide 4 having an oxygen defect structure. The film thickness was about 5000 °.

【0009】このようにして得られた一酸化炭素検出素
子を種々の濃度のCOおよびO2 の混合ガスに接触させ
た。さらに前記一酸化炭素検出素子を図2に示す抵抗加
熱体5により加熱し、CO吸着および吸収の温度依存性
を調べた。入口濃度がCO50ppm、酸素10%の時の
出口CO濃度の測定結果を図3に示す。図3より約30
0℃において最も吸着しており、入口CO濃度の約30
%が吸着していることがわかる。
The carbon monoxide sensing element thus obtained was brought into contact with various concentrations of a mixed gas of CO and O 2. Further, the carbon monoxide detecting element was heated by the resistance heater 5 shown in FIG. 2, and the temperature dependence of CO adsorption and absorption was examined. FIG. 3 shows the measurement results of the outlet CO concentration when the inlet concentration is 50 ppm CO and the oxygen concentration is 10%. Approx. 30 from Fig. 3
It is most adsorbed at 0 ° C. and has an inlet CO concentration of about 30
% Is adsorbed.

【0010】次に温度を300℃に保ち、入口酸素濃度
を変化させたときの出口CO濃度の測定結果を図4に示
す。図4より酸素濃度が変化してもCO濃度は一定であ
ることが判る。
Next, FIG. 4 shows the measurement results of the outlet CO concentration when the temperature was kept at 300 ° C. and the inlet oxygen concentration was changed. FIG. 4 shows that the CO concentration is constant even when the oxygen concentration changes.

【0011】次に約300℃に保ちながら、種々の濃度
のCOガスに接触させ、前記櫛形電極2、3に高周波を
印加し、COの吸着により変化する周波数を調べた。各
CO濃度における周波数の変化を図5に示す。図5より
COが吸着するために周波数が小さくなることが確認で
きる。これは、金属複合酸化物4のイットリウムバリウ
ム銅酸化物がCOを吸着することにより、重量が増加
し、伝播速度が遅くなり、その結果、周波数が小さくな
ると考えられる。つまり、周波数の変化によりCOの吸
着量を知ることができ、単位時間当たりの周波数変化よ
りCOの濃度を検知することができる。図6にCOの濃
度とともに周波数変化が大きくなることを示す。
Next, while maintaining the temperature at about 300 ° C., it was brought into contact with various concentrations of CO gas, and a high frequency was applied to the comb-shaped electrodes 2 and 3, and the frequency changed by CO adsorption was examined. FIG. 5 shows a change in frequency at each CO concentration. From FIG. 5, it can be confirmed that the frequency is reduced due to the adsorption of CO. This is considered to be because the yttrium barium copper oxide of the metal composite oxide 4 adsorbs CO, thereby increasing the weight and slowing down the propagation speed, and as a result, the frequency is reduced. That is, the amount of adsorption of CO can be known from the change in frequency, and the concentration of CO can be detected from the change in frequency per unit time. FIG. 6 shows that the frequency change increases with the CO concentration.

【0012】また、イットリウムバリウム銅酸化物以外
に酸素欠陥構造あるいはペロブスカイト型構造を有する
金属複合酸化物4としてランタンバリウム銅酸化物、ネ
オジウムバリウム銅酸化物およびサマリウムバリウム銅
酸化物等があるが、各々同様に一酸化炭素の濃度を検知
することができた。
In addition to yttrium barium copper oxide, lanthanum barium copper oxide, neodymium barium copper oxide, samarium barium copper oxide and the like are examples of metal composite oxides 4 having an oxygen defect structure or a perovskite structure. Similarly, the concentration of carbon monoxide could be detected.

【0013】[0013]

【発明の効果】以上説明したように本発明の一酸化炭素
検出素子は、圧電基板と弾性波を励震するための電極
と、弾性波伝播路上に配置したCOを選択的に吸着およ
び吸収する金属複合酸化物とから成り、CO吸着および
吸収による周波数の変化よりCOの濃度を検出すること
ができる。
As described above, the carbon monoxide detecting element according to the present invention selectively absorbs and absorbs the piezoelectric substrate, the electrodes for exciting the elastic wave, and the CO disposed on the elastic wave propagation path. It is composed of a metal composite oxide, and the concentration of CO can be detected from a change in frequency due to CO adsorption and absorption.

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

【図1】本発明の一酸化炭素検出素子の上面図FIG. 1 is a top view of a carbon monoxide detecting element of the present invention.

【図2】本発明の一酸化炭素検出素子の下面図FIG. 2 is a bottom view of the carbon monoxide detecting element of the present invention.

【図3】各温度における素子のCO吸着特性を示す図FIG. 3 is a diagram showing CO adsorption characteristics of an element at each temperature.

【図4】入口酸素濃度変化に対する出口CO濃度を示す
FIG. 4 is a graph showing outlet CO concentration with respect to inlet oxygen concentration change.

【図5】各CO濃度における周波数の変化を示す図FIG. 5 is a diagram showing a change in frequency at each CO concentration.

【図6】CO濃度に対する単位時間当たりの周波数変化
量の関係を示す図
FIG. 6 is a diagram showing a relationship between a CO concentration and a frequency change amount per unit time.

【符号の説明】[Explanation of symbols]

1 圧電基板 2 櫛形電極(入力側) 3 櫛形電極(出力側) 4 金属複合酸化物 5 抵抗加熱体 DESCRIPTION OF SYMBOLS 1 Piezoelectric substrate 2 Comb electrode (input side) 3 Comb electrode (output side) 4 Metal composite oxide 5 Resistance heater

───────────────────────────────────────────────────── フロントページの続き (72)発明者 黄地 謙三 大阪府門真市大字門真1006番地 松下電 器産業株式会社内 (56)参考文献 特開 平2−35352(JP,A) 特開 平3−248057(JP,A) 特開 平4−307351(JP,A) (58)調査した分野(Int.Cl.7,DB名) G01N 29/00 - 29/28 JICSTファイル(JOIS)────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Kenzo Koji 1006 Kazuma Kadoma, Kadoma City, Osaka Prefecture Matsushita Electric Industrial Co., Ltd. (56) References JP-A-2-35352 (JP, A) JP-A-3 −248057 (JP, A) JP-A-4-307351 (JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) G01N 29/00-29/28 JICST file (JOIS)

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】圧電基板と、前記圧電基板上に形成された
弾性波を励振するための電極と、弾性波伝播路上に配置
した一酸化炭素(CO)を吸着および吸収する金属複合
酸化物とから成る一酸化炭素検出素子。
1. A piezoelectric substrate, an electrode for exciting an elastic wave formed on the piezoelectric substrate, and a metal composite oxide disposed on an elastic wave propagation path for adsorbing and absorbing carbon monoxide (CO). A carbon monoxide detection element comprising:
【請求項2】前記金属複合酸化物は、酸素欠陥構造ある
いはペロブスカイト型構造であることを特徴とする請求
項1記載の一酸化炭素検出素子。
2. The carbon monoxide detecting element according to claim 1, wherein said metal composite oxide has an oxygen deficiency structure or a perovskite structure.
【請求項3】素子の動作温度範囲は200〜300℃で
あることを特徴とする請求項1記載の一酸化炭素検出素
子。
3. An element for detecting carbon monoxide according to claim 1, wherein the operating temperature range of the element is 200 to 300 ° C.
【請求項4】圧電基板上には、抵抗加熱体が形成されて
いることを特徴とする請求項1記載の一酸化炭素検出素
子。
4. A carbon monoxide detecting element according to claim 1, wherein a resistance heating element is formed on the piezoelectric substrate.
JP04354893A 1993-03-04 1993-03-04 Carbon monoxide detector Expired - Fee Related JP3301144B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP04354893A JP3301144B2 (en) 1993-03-04 1993-03-04 Carbon monoxide detector

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP04354893A JP3301144B2 (en) 1993-03-04 1993-03-04 Carbon monoxide detector

Publications (2)

Publication Number Publication Date
JPH06258210A JPH06258210A (en) 1994-09-16
JP3301144B2 true JP3301144B2 (en) 2002-07-15

Family

ID=12666815

Family Applications (1)

Application Number Title Priority Date Filing Date
JP04354893A Expired - Fee Related JP3301144B2 (en) 1993-03-04 1993-03-04 Carbon monoxide detector

Country Status (1)

Country Link
JP (1) JP3301144B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5992215A (en) * 1997-05-29 1999-11-30 Sensor Research And Development Corp. Surface acoustic wave mercury vapor sensors
JP3997642B2 (en) * 1999-02-24 2007-10-24 トヨタ自動車株式会社 Carbon monoxide concentration detection apparatus and carbon monoxide concentration detection method
JP5231914B2 (en) * 2007-09-27 2013-07-10 独立行政法人産業技術総合研究所 Oxidizing active chemical species sensor, oxidizing active chemical species abundance measuring method, and oxidizing active chemical species abundance measuring apparatus

Also Published As

Publication number Publication date
JPH06258210A (en) 1994-09-16

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