首页> 外文期刊>Journal of clinical monitoring and computing >Improving accuracy of the chemiluminescent analyser for measurement of nitric oxide and nitrogen dioxide in respired gas.
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Improving accuracy of the chemiluminescent analyser for measurement of nitric oxide and nitrogen dioxide in respired gas.

机译:提高了化学发光分析仪测量呼吸气体中一氧化氮和二氧化氮的准确性。

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OBJECTIVE: The aim of this study was to improve the accuracy of the chemiluminescent analyser in the measurement of nitric oxide (NO) and nitrogen dioxide (NO2) in both dry and humidified gas mixtures containing oxygen (O2) in varying concentrations. This work was performed because initial attempts to determine rate constants for the decay of NO and rates of formation of NO2 were unsuccessful. METHODS: Equations were developed by which the raw output signal of the analyser could be corrected for errors arising from variations in sensitivity of the analysis cell, degree of conversion of NO2 to NO and degradation of NO to nitrogen (N2) in the converter prior to analysis. Once correction factors were derived from calibration, the analyser was used to measure rate of decay of 40 ppm nitric oxide in both dry and humidified gases containing either 21%, 60% or 100% O2 in N2. RESULTS: Correction factors obtained from calibration corrected falls in sensitivity to a maximum of 28%, variations in degree of conversion of NO2 to NO from 62-96% and degradation of NO from 2-8% in the converter before analysis depending on O2 concentration and humidification. When the calibrated machine was used to measure decay of NO, an excellent fit (r2 > 0.95) with a hyperbolic function was obtained confirming that rate of decay is proportional to oxygen O2 concentration and square of NO concentration. A rate constant per unit O2 concentration of 9.40E-10 ppm(-2) min(-1) for humidified gas was significantly higher than 8.27E-10 ppm(-2) min(-1) for "dry" gas (P = 0.008) at 22 degrees C. Rise in NO2 predicted from the "wet" rate constant achieved 3ppm in 65 seconds with 40 ppm NO in 100% oxygen and 107 sec. in 60% oxygen. CONCLUSION: This study indicates that for accurate analysis of NO and NO2 concentrations in airway gases a rigorous calibration of the instrument for the conditions applying in the experiment is mandatory. Once this is achieved the instrument is capable of precise analysis of both gases.
机译:目的:本研究的目的是提高化学发光分析仪在测量不同浓度的含氧(O2)的干燥和加湿混合气体中的一氧化氮(NO)和二氧化氮(NO2)的准确性。进行这项工作的原因是,最初无法确定NO衰减的速率常数和NO2的生成速率。方法:开发了方程,通过该方程可以校正分析仪原始输出信号的误差,该误差是由分析池灵敏度变化,转化器中NO2转化为NO的程度和转化器中NO转化为氮(N2)的变化所引起的。分析。一旦从校准中得出校正因子,就可以使用分析仪测量在N2中含有21%,60%或100%O2的干燥和加湿气体中40 ppm一氧化氮的衰减率。结果:在分析之前,根据氧气浓度,通过校正后的校正得出的校正因子灵敏度最高下降到28%,转化器中NO2转化为NO的程度从62-96%变化,NO降解为2-8%。和加湿。当使用校准的机器来测量NO的衰减时,获得了具有双曲线函数的极佳拟合(r2> 0.95),这证实了衰减速率与氧气O2浓度和NO浓度的平方成正比。对于湿气,每单位O2浓度为9.40E-10 ppm(-2)min(-1)的速率常数显着高于“干”气的8.27E-10 ppm(-2)min(-1)(P = 0.008)在22℃。根据“湿”速率常数预测的NO 2的增加在65秒内达到3ppm,在100%氧气中为40ppm NO和107秒。在60%的氧气中。结论:这项研究表明,为了准确分析气道气体中的NO和NO2浓度,必须对仪器进行严格的校准,以适应实验中使用的条件。一旦做到这一点,该仪器就能够对两种气体进行精确分析。

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