Metalloporphyrins immobilized in styrene-trifluoroethylmethacrylate copolymer film as an optical oxygen sensing probe

被引:31
作者
Amao, Y
Miyashita, T
Okura, I
机构
[1] Natl Aerosp Lab, Fluid Sci Res Ctr, Tokyo 1828522, Japan
[2] Tohoku Univ, Inst Chem React Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
[3] Tokyo Inst Technol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 2268501, Japan
关键词
metalloporphyrin; optical oxygen sensing; phosphorescence; fluoropolymer;
D O I
10.1002/jpp.321
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of new fluoropolymer, poly(styrene-co-trifluoroethylmethacrylate) (poly-Sty(n)-co-TFEMm), with different composition ratios of Sty and TFEM units, is synthesized and applied to the matrix of an optical oxygen sensing probe using phosphorescence quenching of metalloporphyrins, platinum and palladium octaethylporphyrin (PtOEP and PdOEP), by oxygen. The phosphorescence intensity of PtOEP and PdOEP in poly-Sty(n)-co-TFEMm film decreased with increase of oxygen concentration. The ratio I-0/I-100 is used as a sensitivity of the sensing film, where I-0 and I-100 represent the detected phosphorescence intensities from a film exposed to 100% argon and 100% oxygen, respectively. For PtOEP in poly-Sty(n)-co-TFEMm film, I-0/I-100 ratios are more than 20.6 and large Stern-Volmer constants greater than 0.49%(-1) are obtained compared with PtOEP in PS film. For PdOEP in poly-Sty(n)-co-TFEMm film, on the other hand, large I-0/I-100 values greater than 188.7 are obtained. In both cases for PtOEP and PdOEP, I-0/I-100 values increased with increase of the number of TFEM units in poly-Sty(n)-co-TEEMm. The response times of PtOEP and PdOEP immobilized in poly-Sty(1)-co-TFEM2.50 films are 5.5 and 3.0 s on going from argon to oxygen and 90.0 and 143 s from oxygen to argon, respectively. These results show that PtOEP and PdOEP immobilized in poly Sty(n)-co-TFEMm films are highly sensitive devices for oxygen. Copyright (C) 2001 John Wiley & Sons, Ltd.
引用
收藏
页码:433 / 438
页数:6
相关论文
共 34 条
[1]  
[Anonymous], ANAL CHEM
[2]   A MICRO-HOLE POTENTIOSTATIC OXYGEN SENSOR FOR OCEANIC CTDS [J].
ATKINSON, MJ ;
THOMAS, FIM ;
LARSON, N ;
TERRILL, E ;
MORITA, K ;
LIU, CC .
DEEP-SEA RESEARCH PART I-OCEANOGRAPHIC RESEARCH PAPERS, 1995, 42 (05) :761-&
[3]   DETERMINATION OF OXYGEN CONCENTRATIONS BY LUMINESCENCE QUENCHING OF A POLYMER-IMMOBILIZED TRANSITION-METAL COMPLEX [J].
BACON, JR ;
DEMAS, JN .
ANALYTICAL CHEMISTRY, 1987, 59 (23) :2780-2785
[4]   LUMINESCENCE QUENCHING MECHANISM FOR MICROHETEROGENEOUS SYSTEMS [J].
CARRAWAY, ER ;
DEMAS, JN ;
DEGRAFF, BA .
ANALYTICAL CHEMISTRY, 1991, 63 (04) :332-336
[5]  
CLARK LC, 1956, T AM SOC ART INT ORG, V2, P41
[6]   MODELING OF LUMINESCENCE QUENCHING-BASED SENSORS - COMPARISON OF MULTISITE AND NONLINEAR GAS SOLUBILITY MODELS [J].
DEMAS, JN ;
DEGRAFF, BA ;
XU, WY .
ANALYTICAL CHEMISTRY, 1995, 67 (08) :1377-1380
[7]   OXYGEN PROBE BASED ON TETRAKIS(ALKYLAMINO)ETHYLENE CHEMI-LUMINESCENCE [J].
FREEMAN, TM ;
SEITZ, WR .
ANALYTICAL CHEMISTRY, 1981, 53 (01) :98-102
[8]   LUMINESCENCE QUENCHING BEHAVIOR OF AN OXYGEN SENSOR-BASED ON A RU(II) COMPLEX DISSOLVED IN POLYSTYRENE [J].
HARTMANN, P ;
LEINER, MJP ;
LIPPITSCH, ME .
ANALYTICAL CHEMISTRY, 1995, 67 (01) :88-93
[9]  
Hendricks H.D., 1973, US Pat., Patent No. 3709663
[10]   PHOTOLUMINESCENCE OF PYRENEBUTYRIC ACID INCORPORATED INTO SILICONE FILM AS A TECHNIQUE IN LUMINESCENT OXYGEN SENSING [J].
ISHIJI, T ;
KANEKO, M .
ANALYST, 1995, 120 (06) :1633-1638