A Numerical Procedure for Multivariate Calibration Using Heteroscedastic Principal Components Regression

Processes

Alessandra da Rocha Duailibe Monteiro¹  Thiago de Sá Feital²  José Carlos Pinto² 

[1] Departamento de Engenharia Química e Petróleo (TEQ), Universidade Federal Fluminense, Niterói, Rio de Janeiro CEP 24210-240, RJ, Brazil;OPTIMATECH LTDA, Rio de Janeiro CEP 21941-614, RJ, Brazil;

关键词: heteroscedastic principal components regression (H-PCR);    measurement error;    multivariate analysis;    numerical procedure;    near infrared spectroscopy (NIRS);   

DOI  :  10.3390/pr9091686

来源: DOAJ

【 摘 要 】

Many methods have been developed to allow for consideration of measurement errors during multivariate data analyses. The incorporation of the error structure into the analytical framework, usually described in terms of the covariance matrix of measurement errors, can provide better model estimation and prediction. However, little effort has been made to evaluate the effects of heteroscedastic measurement uncertainties on multivariate analyses when the covariance matrix of measurement errors changes with the measurement conditions. For this reason, the present work describes a new numerical procedure for analyses of heteroscedastic systems (heteroscedastic principal component regression or H-PCR) that takes into consideration the variations of the covariance matrix of measurement fluctuations. In order to illustrate the proposed approach, near infrared (NIR) spectra of xylene and toluene mixtures were measured at different temperatures and stirring velocities and the obtained data were used to build calibration models with different multivariate techniques, including H-PCR. Modeling of available xylene–toluene NIR data revealed that H-PCR can be used successfully for calibration purposes and that the principal directions obtained with the proposed approach can be quite different from the ones calculated through standard PCR, when heteroscedasticity is disregarded explicitly.

【 授权许可】

Unknown