JPS6038661B2 - oxygen concentration detector - Google Patents

oxygen concentration detector

Info

Publication number
JPS6038661B2
JPS6038661B2 JP53091932A JP9193278A JPS6038661B2 JP S6038661 B2 JPS6038661 B2 JP S6038661B2 JP 53091932 A JP53091932 A JP 53091932A JP 9193278 A JP9193278 A JP 9193278A JP S6038661 B2 JPS6038661 B2 JP S6038661B2
Authority
JP
Japan
Prior art keywords
oxygen concentration
exhaust gas
concentration detector
electrodes
platinum
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
Application number
JP53091932A
Other languages
Japanese (ja)
Other versions
JPS5518954A (en
Inventor
毅 西
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.)
Toyota Motor Corp
Panasonic Holdings Corp
Original Assignee
Toyota Motor 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 Toyota Motor Corp, Matsushita Electric Industrial Co Ltd filed Critical Toyota Motor Corp
Priority to JP53091932A priority Critical patent/JPS6038661B2/en
Publication of JPS5518954A publication Critical patent/JPS5518954A/en
Publication of JPS6038661B2 publication Critical patent/JPS6038661B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Measuring Oxygen Concentration In Cells (AREA)

Description

【発明の詳細な説明】 本発明の主たる目的は、酸素濃度検出器の性能,信頼性
の向上を可能にすることを目的とする。
DETAILED DESCRIPTION OF THE INVENTION The main object of the present invention is to make it possible to improve the performance and reliability of an oxygen concentration detector.

従来の酸素濃度検出器においては、例えば管状ジルコニ
ア固体電解質より構成される酸素濃度検出素子の電極と
して、大気側ならびに排気ガス側に、化学メッキ、蒸着
、熱分解等の方法にて薄膜状の白金(Pt)電極を設け
ている。
In conventional oxygen concentration detectors, for example, a thin platinum film is coated on the atmosphere side and exhaust gas side by chemical plating, vapor deposition, thermal decomposition, etc. as an electrode of an oxygen concentration detection element made of a tubular zirconia solid electrolyte. (Pt) electrodes are provided.

従来の検出器において、上記電極として種々の方法によ
り得る該薄膜状白金電極で例えば塩化白金酸(日2・P
tCそb・母LO)等の熱分解法により生成した薄膜状
白金は、他の方法と比較して耐久寿命性が優れている。
In conventional detectors, the thin film platinum electrode obtained by various methods is used as the electrode.
Thin film platinum produced by thermal decomposition methods such as tCSOb and LO) has superior durability compared to other methods.

この熱分解条件として、例えば還元雰囲気、酸化雰囲気
中で白金の生成を行つていた。しかし、該酸素濃度検出
器の特性として、特に応答性が遅く基本特性的には十分
でないという問題がある。
As the thermal decomposition conditions, for example, platinum was produced in a reducing atmosphere or an oxidizing atmosphere. However, the oxygen concentration detector has a problem in that its response is particularly slow and its basic characteristics are insufficient.

また、耐久寿命試験において、高温の排ガス中に長時間
さらすと、応答性が速くなる良化煩向が見られたが十分
な特性ではなかった。そこで、この問題を解決するため
に、この耐久寿命試験において特性良化する原因を調べ
た結果、排ガス側白金電極が排ガス雰囲気により活性化
されたものと判明した。この電極表面の活性化は機械的
な処理、例えば表面を粗化し三相界面を増やす等の工法
が考えられ、基本特性的に十分なものを得ることができ
る。
In addition, in the durability test, when exposed to high-temperature exhaust gas for a long time, there was a tendency for the response to become faster, but the characteristics were not sufficient. Therefore, in order to solve this problem, we investigated the cause of the improvement in characteristics in this durability test and found that the platinum electrode on the exhaust gas side was activated by the exhaust gas atmosphere. This activation of the electrode surface can be achieved by mechanical treatment, such as roughening the surface and increasing the number of three-phase interfaces, and it is possible to obtain sufficient basic characteristics.

しかし、表面組化により酸素濃度検出素子の表面に微細
なクラックが形成され、このために機械的強度が不足し
、振動を受ける場所で長時間使用すると該酸素濃度検出
素子が破損する等耐久性に難点を有している。
However, due to surface assembling, minute cracks are formed on the surface of the oxygen concentration detection element, resulting in insufficient mechanical strength, and durability such as damage to the oxygen concentration detection element when used for a long time in a place subject to vibration. It has some drawbacks.

本発明は以上の点に鑑み、酸素濃度検出素子に形成され
る白金電極として、ガソリン燃焼炎の燃料過剰雰囲気中
で熱分解法による白金電極を生成することにより得られ
た白金薄膜電極を有する構成とし、基本特性,耐久性の
よい酸素濃度検出器を提供することを目的とするもので
ある。
In view of the above points, the present invention has a configuration in which a platinum electrode formed in an oxygen concentration detection element includes a platinum thin film electrode obtained by producing a platinum electrode by a pyrolysis method in an excess fuel atmosphere of a gasoline combustion flame. The purpose is to provide an oxygen concentration detector with good basic characteristics and durability.

以下、本発明を図に示す実施例について説明する。DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, embodiments of the present invention shown in the drawings will be described.

第1図は酸素濃度検出器の断面図である。FIG. 1 is a sectional view of the oxygen concentration detector.

管状のジルコニア固体電解質1は大気側薄膜白金電極2
と排ガス側薄膜白金電極3により形成されている。本実
施例の1つは電極2,3に用いる材料の塩化白金酸(舷
PtCそ6・母LO)と無水エチルアルコールを比重1
.0〜1.5になるように混合した液を用い、デイツプ
により該電極2,3を同時に浸潰した。この酸素濃度検
出素子を空気中にて250oo、3び分乾燥後、ガソリ
ン燃焼炎550qo〜1100℃の雰囲気条件として空
気過剰率入が0.8〜0.9、CO濃度約3〜1%の範
囲で20〜60分熱することにより、塩化白金酸から白
金に分解される。この分解後各電極表面の導通性を測定
し抵抗値で0〜200Qの範囲になるまで電極液の浸薄
「乾燥t分籍を繰り返す。これにより白金電極2,3が
形成される。このようにして生成された薄膜状白金電極
の表面状態は、排ガス中の酸素濃度を測定する検出器と
して活性な状態に仕上がり、基本特性,耐久性において
も従来の熱分解法で得られた酸素濃度検出器の性能とし
て比較しても第2図(Aは従来の代表特性、Bは本発明
の実施例にもとづく特性)に耐久寿命特性を示すように
極めて優れた特性を示すものであり、実用性の大なるも
のである。
The tubular zirconia solid electrolyte 1 has a thin film platinum electrode 2 on the atmosphere side.
and a thin film platinum electrode 3 on the exhaust gas side. One of the present examples is that the materials used for electrodes 2 and 3, chloroplatinic acid (PtC 6, base LO), and anhydrous ethyl alcohol are mixed with a specific gravity of 1
.. The electrodes 2 and 3 were simultaneously immersed in a dip using a liquid mixed so as to have a concentration of 0 to 1.5. After drying this oxygen concentration detection element in air for 3 minutes at 250 oo, the atmospheric conditions include a gasoline combustion flame of 550 qo to 1100°C, an excess air ratio of 0.8 to 0.9, and a CO concentration of approximately 3 to 1%. By heating in the range of 20 to 60 minutes, chloroplatinic acid is decomposed into platinum. After this decomposition, the conductivity of each electrode surface is measured and the dipping and drying process of the electrode solution is repeated until the resistance value is in the range of 0 to 200Q.The platinum electrodes 2 and 3 are thereby formed. The surface state of the thin film platinum electrode produced in this process is now active as a detector for measuring oxygen concentration in exhaust gas, and its basic characteristics and durability are superior to those obtained by conventional thermal decomposition methods. Comparing the performance of the device, it shows extremely excellent characteristics as shown in Figure 2 (A is the typical characteristic of the conventional one, B is the characteristic based on the example of the present invention), and shows extremely excellent durability characteristics. It is a great thing.

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

第1図は本発明の一実施例になる酸素濃度検出器の断面
図、第2図は本発明の一実施例と従来の代表的な酸素濃
度検出器の耐久寿命特性の比較図である。 1…・・・ジルコニア固体電解質「 2…・・,大気側
薄膜状白金電極、3・・・・・・排ガス側薄膜状白金電
極。 第1図第2図
FIG. 1 is a sectional view of an oxygen concentration detector according to an embodiment of the present invention, and FIG. 2 is a comparison diagram of the durability characteristics of an embodiment of the present invention and a typical conventional oxygen concentration detector. 1... Zirconia solid electrolyte 2... Thin film platinum electrode on the atmosphere side, 3... Thin film platinum electrode on the exhaust gas side. Fig. 1 Fig. 2

Claims (1)

【特許請求の範囲】[Claims] 1 ジルコニア固体電解質の内燃機関の排ガスと大気と
のそれぞれの界面に対向した電極が形成され、その排ガ
ス面には多孔質の白金からなる触媒電極を有し、排ガス
中の酸素濃度を大気の酸素濃度と比較して排ガス中の空
燃比を検出する酸素濃度検出器において、該ジルコニア
固体電解質の内外面の電極をガソリン燃焼炎の燃料過剰
雰囲気中で熱分解により生成した薄膜白金電極で構成し
たことを特徴とする酸素濃度検出器。
1 Opposed electrodes are formed at each interface between the exhaust gas of an internal combustion engine made of a zirconia solid electrolyte and the atmosphere, and a catalyst electrode made of porous platinum is provided on the exhaust gas surface to adjust the oxygen concentration in the exhaust gas to the atmospheric oxygen. In an oxygen concentration detector that detects the air-fuel ratio in exhaust gas by comparing it with the concentration, the electrodes on the inner and outer surfaces of the zirconia solid electrolyte are composed of thin film platinum electrodes produced by thermal decomposition in the fuel-excess atmosphere of a gasoline combustion flame. An oxygen concentration detector featuring:
JP53091932A 1978-07-26 1978-07-26 oxygen concentration detector Expired JPS6038661B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP53091932A JPS6038661B2 (en) 1978-07-26 1978-07-26 oxygen concentration detector

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP53091932A JPS6038661B2 (en) 1978-07-26 1978-07-26 oxygen concentration detector

Publications (2)

Publication Number Publication Date
JPS5518954A JPS5518954A (en) 1980-02-09
JPS6038661B2 true JPS6038661B2 (en) 1985-09-02

Family

ID=14040355

Family Applications (1)

Application Number Title Priority Date Filing Date
JP53091932A Expired JPS6038661B2 (en) 1978-07-26 1978-07-26 oxygen concentration detector

Country Status (1)

Country Link
JP (1) JPS6038661B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63127763U (en) * 1987-02-13 1988-08-22
JPH02118664U (en) * 1989-03-06 1990-09-25

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63127763U (en) * 1987-02-13 1988-08-22
JPH02118664U (en) * 1989-03-06 1990-09-25

Also Published As

Publication number Publication date
JPS5518954A (en) 1980-02-09

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