Atwater J E, DeHart J, Wheeler R R
UMPQUA Research Company, Myrtle Creek, OR 97457, USA.
J Biolumin Chemilumin. 1998 May-Jun;13(3):125-30. doi: 10.1002/(SICI)1099-1271(199805/06)13:3<125::AID-BIO475>3.0.CO;2-E.
Dissolved elemental oxygen is determined in a flowing aqueous stream using glucose oxidase to catalyse the reaction between D-glucose and O2 to produce hydrogen peroxide. The levels of the resulting H2O2 are detected and quantified by luminol chemiluminescence using in-line solid phase media for pH adjustment of the reagent stream and for controlled release of the luminophore. The reaction is initiated by electrochemical catalysis. By the use of excess D-glucose in the reagent flow stream, the intensity of chemiluminescence is rendered proportional only to fluctuations in the dissolved O2 concentration. The methodology provides a means for the detection of aqueous O2 in the range 0-10 mg/L.
使用葡萄糖氧化酶催化D - 葡萄糖与O₂之间的反应以产生过氧化氢,从而测定流动水流中溶解的元素氧。通过鲁米诺化学发光检测并定量生成的H₂O₂水平,使用在线固相介质对试剂流进行pH调节并控制发光体的释放。该反应由电化学催化引发。通过在试剂流中使用过量的D - 葡萄糖,化学发光强度仅与溶解氧浓度的波动成比例。该方法提供了一种检测0 - 10 mg/L范围内水溶氧的手段。