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    • 6. 发明专利
    • CO SENSOR
    • JPH095280A
    • 1997-01-10
    • JP17942095
    • 1995-06-22
    • GASTAR CORPYAZAKI CORP
    • ENOMOTO MASANORIKIMURA SHINGOSHIGEOKA TAKUJIYASUGATA KAZUTOSHIOGINO KAORUOISHI KAZUHIRO
    • G01N27/16
    • PURPOSE: To provide a CO sensor which facilitates manufacture of its cover and does not receive bad influence of flow velocity of exhaust gas. CONSTITUTION: A CO detection mechanism part 3 provided with a comparative element 4 and a detection element is formed on the surface side of a sensor base 1, and coated with a cover 35 covered on the sensor base 1. The cover 35 is constituted by a composite material of a filter material 15 and a mesh 16 sandwiching the surface and the rear surface of the filter material 15 with the mesh 16. Small through holes are scatteringly formed on the filter material 15. Exhaust gas passes through the mesh 16 and the filter material 15, is introduced into the cover 35 in a state of almost zero flow velocity, and CO concentration in the exhaust gas is detected by the CO detection mechanism part 3 in the state which has no influence of the flow velocity. Even if the exhaust gas is stopped through the filter material 15, it enters the cover 35 through the small through holes 40 and the detection of the CO concentration is made possible without hindrance.
    • 8. 发明专利
    • PEROVSKITE TYPE OXIDE SEMICONDUCTOR OXYGEN SENSOR
    • JPS60225051A
    • 1985-11-09
    • JP8107484
    • 1984-04-24
    • YAZAKI CORP
    • SEIYAMA TETSUOARAI HIROMICHINITA HOZUMIYASUGATA KAZUTOSHI
    • G01N27/12H01B3/12
    • PURPOSE:To attain miniaturization of the titled oxygen sensor, by using Srx Na1-xTiO3(x>0.9) obtained by applying valency control by a typical element of Na to SrTiO3 or Sr of SrTiO3. CONSTITUTION:For example, a material having a perovskite structure ABO3 and showing an oxide semiconductive property is prepared as follows. At first, with respect to the preparation of SrTiO3, special grade reagents of SrCO3 and TiO2 are used and sufficiently dried at about 100-150 deg.C while the dried reagents are weighed on the basis of a stoichiometric composition and mixed, crushed and calcined at 1,000-1,200 deg.C for 2-3hr to obtain SrTiO3. This SiTiO3 is sufficiently crushed in an agate mortar and, thereafter, molded under pressure of 60- 120kg/cm to form a pellet having a diameter of about 10mm. and a thickness of 1-2mm. while the pellet is heated to 1,000-1,200 deg.C at a heating speed of 10 deg.C/min to be held at that temp. for 3-6hr and cooled at a speed of 10 deg.C/min to perform sintering. Further, a Pt-paste is baked onto the pellet to form an electrode and a Pt or Au wire is taken out as a lead wire. Furthermore, Sr0.997Na0.003TiO3, wherein valency control is applied to Sr of SrTiO3 by Na, is prepared by the same mfg. method as SiTiO3 by using anhydrous Na2CO3.