1999
DOI: 10.1016/s0021-9673(99)00537-3
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Sources of uncertainty in gas chromatography and high-performance liquid chromatography

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Cited by 83 publications
(44 citation statements)
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“…These certificates report each substance concentration, along with their expanded uncertainty (U) and the corresponding coverage factors (k), and these concentrations are the input variables of each measurement model. Uncertainty in chromatographic measurement may come from multiple sources including material injection to the machine, temperature control of the gas chromatograph, material adsorption in the lines upstream to the columns, and the detection process by sensors [17]. The effect of all these sources is manifested every time when the chromatograph is operated; for that reason, several replicas were done for each RM and for each sample, and the multiple values obtained of the areas were used to estimate the uncertainties corresponding to the input quantities y 0 and y i (y 1 , y 2 , and y 3 ).…”
Section: Identification and Estimation Of The Sources Of Uncertaintymentioning
confidence: 99%
“…These certificates report each substance concentration, along with their expanded uncertainty (U) and the corresponding coverage factors (k), and these concentrations are the input variables of each measurement model. Uncertainty in chromatographic measurement may come from multiple sources including material injection to the machine, temperature control of the gas chromatograph, material adsorption in the lines upstream to the columns, and the detection process by sensors [17]. The effect of all these sources is manifested every time when the chromatograph is operated; for that reason, several replicas were done for each RM and for each sample, and the multiple values obtained of the areas were used to estimate the uncertainties corresponding to the input quantities y 0 and y i (y 1 , y 2 , and y 3 ).…”
Section: Identification and Estimation Of The Sources Of Uncertaintymentioning
confidence: 99%
“…26,27 As modificações apresentadas foram escolhidas na faixa que pode ser usualmente esperada quando há transferência do método entre laboratórios diferentes. O teste de robustez foi executado na mesma amostra do plano interlaboratorial, em 3 dias consecutivos: 1º dia, 2º dia e 3º dia.…”
Section: Teste De Robustezunclassified
“…In an ideal case, peaks are narrow and follow a Gaussian distribution. However, several factors are contributing to peak broadening like detector, column, mobile phase, injection, column temperature and flow rate [2]. To get an optimal performance of the LC, GC or SFC system the theoretical plate height (HETP) should be minimized.…”
Section: Introductionmentioning
confidence: 99%