Comparison of Two Different Approaches toward Model Transferability in NIR Spectroscopy

1998 ◽  
Vol 52 (1) ◽  
pp. 7-16 ◽  
Author(s):  
H. Swierenga ◽  
W. G. Haanstra ◽  
A. P. De Weijer ◽  
L. M. C. Buydens

Recently, efficient methods have become available to transfer a multivariate calibration model from one instrument to another. Two categories can be distinguished: improvement of the robustness of the calibration model by, for example, a proper data preprocessing; and adaptation of the calibration model by, for example, (piecewise) direct standardization. In direct standardization, a subset from the calibration set should be measured on both instruments. Usually, however, the calibration samples cannot be measured on both instruments. When data preprocessing is applied to the transfer of multivariate calibration models, there is no need for remeasurement of a subset on both instruments. In this paper, both categories are compared for the determination of the component concentrations in a ternary mixture of methanol, ethanol, and 1-propanol using NIR spectroscopy. The calibration models obtained on one instrument are transferred to other NIR instruments. It has been found that the results of proper data preprocessing are comparable with the results obtained by direct standardization when the models are transferred over three NIR instruments.

Energies ◽  
2019 ◽  
Vol 12 (13) ◽  
pp. 2497 ◽  
Author(s):  
José Luis Fernández ◽  
Felicia Sáez ◽  
Eulogio Castro ◽  
Paloma Manzanares ◽  
Mercedes Ballesteros ◽  
...  

The determination of chemical composition of lignocellulose biomass by wet chemistry analysis is labor-intensive, expensive, and time consuming. Near infrared (NIR) spectroscopy coupled with multivariate calibration offers a rapid and no-destructive alternative method. The objective of this work is to develop a NIR calibration model for olive tree lignocellulosic biomass as a rapid tool and alternative method for chemical characterization of olive tree pruning over current wet methods. In this study, 79 milled olive tree pruning samples were analyzed for extractives, lignin, cellulose, hemicellulose, and ash content. These samples were scanned by reflectance diffuse near infrared techniques and a predictive model based on partial least squares (PLS) multivariate calibration method was developed. Five parameters were calibrated: Lignin, cellulose, hemicellulose, ash, and extractives. NIR models obtained were able to predict main components composition with R2cv values over 0.5, except for lignin which showed lowest prediction accuracy.


The Analyst ◽  
2003 ◽  
Vol 128 (9) ◽  
pp. 1204-1207 ◽  
Author(s):  
Márcia C. Breitkreitz ◽  
Ivo M. Raimundo, Jr ◽  
Jarbas J. R. Rohwedder ◽  
Celio Pasquini ◽  
Heronides A. Dantas Filho ◽  
...  

2018 ◽  
Vol 9 (4) ◽  
pp. 400-407 ◽  
Author(s):  
Selvia Maged Adly ◽  
Maha Mohamed Abdelrahman ◽  
Nada Sayed Abdelwahab ◽  
Nourudin Wageh Ali

In this work, multivariate calibration models and TLC-densitometric methods have been developed and validated for quantitative determination of olmesartan medoxomil (OLM) and hydrochlorothiazide (HCZ) in presence of their degradation products, olmesartan (OL) and salamide (SAL), respectively. In the first method, multivariate calibration models including principal component regression (PCR) and partial least square (PLS) were applied. The wavelength range 210-343 nm was used and data was auto-scaled and mean centered as pre-processing steps for PCR and PLS models, respectively. These models were tested by application to external validation set with mean percentage recoveries 99.78, 100.01, 100.41 and 100.46% for OLM, HCZ, OL and SAL, respectively, for PLS model and also, 100.22, 100.40, 102.25 and 100.13% for them, respectively, for PCR model. The second method is TLC-densitometry at which the chromatographic separation was carried out using silica gel 60F254 TLC plates and the developing system consisted of a mixture of ethyl acetate:chloroform:methanol: formic acid:tri-ethylamine (60:40:4:4:1, by volume) with UV-scanning at 254 nm. The developed methods were successfully applied for determination of OLM and HCZ in their pharmaceutical dosage form. Also, statistical comparison was made between the developed methods and the reported method using student’s-t test and F-test and results showed that there was no significant difference between them concerning both accuracy and precision.


2015 ◽  
Vol 18 (2) ◽  
pp. 145-151
Author(s):  
Chau Minh Huynh ◽  
Thu Du Ly ◽  
Thach Thai Pham ◽  
Tran Thi Bao Pham ◽  
Minh Khanh Duong ◽  
...  

Conventional spectrophotometric methods for simultaneous determination of nickel, lead and zinc in forms of complexes with a reagent is not feasible due to the overlap of their absorption spectra. A multivariate calibration method was used to overcome this problem. In this study, the calibration model was constructed based on absorption spectra of 30 mixture standards in the range from 490 to 600 nm. Factors influencing experimental results such as amount of reagents, pH, and color development time were optimized. The standard calibration ranges for determination of nickel, lead and zinc were found at 0.5-5 ppm. The method was applied for determination of these ions in tap water samples at ppm level, with recoveries (and RSD) of nickel, lead and zinc were 103.3 % (3.0 %), 74.9 % (11.5 %) and 104.6 % (4.6 %), respectively.


2001 ◽  
Vol 73 (4) ◽  
pp. 519-524 ◽  
Author(s):  
KELY VIVIANE DE SOUZA ◽  
PATRICIO PERALTA-ZAMORA

The generation of poly-hydroxilated transient species during the photochemical treatment of phenol usually impedes the spectrophotmetric monitoring of its degradation process. Frequently, the appearance of compounds such as pyrocatechol, hydroquinone and benzoquinone produces serious spectral interference, which hinder the use of the classical univariate calibration process. In this work, the use of multivariate calibration is proposed to permit the spectrophotometric determination of phenol in the presence of these intermediates. Using 20 synthetic mixtures containing phenol and the interferents, a calibration model was developed by using a partial least square regression process (PLSR) and processing the absorbance signal between 180 and 300 nm. The model was validated by using 3 synthetic mixtures. In this operation, typical errors lower than 3% were observed. Close correlation between the results obtained by liquid chromatography and the proposed method was also observed.


2017 ◽  
Vol 63 (No. 5) ◽  
pp. 226-230 ◽  
Author(s):  
Zbíral Jiří ◽  
Čižmár David ◽  
Malý Stanislav ◽  
Obdržálková Elena

Determining and characterizing soil organic matter (SOM) cheaply and reliably can help to support decisions concerning sustainable land management and climate policy. Glomalin was recommended as one of possible indicators of SOM quality. Extracting glomalin from and determining it in soils using classical chemical methods is too complicated and therefore near-infrared spectroscopy (NIRS) was studied as a method of choice for the determination of glomalin. Representative sets of 84 different soil samples from arable land and grasslands and 75 forest soils were used to develop NIRS calibration models. The parameters of the NIRS calibration model (R = 0.90 for soils from arable land and grasslands and R = 0.94 for forest soils) proved that glomalin can be determined in air-dried soils by NIRS with adequate trueness and precision simultaneously with determination of nitrogen and oxidizable carbon.


2012 ◽  
Vol 236-237 ◽  
pp. 83-88 ◽  
Author(s):  
Wei Qiang Luo ◽  
Hai Qing Yang ◽  
Wei Cheng Dai

Ultra-violet, visible and near infrared (UV-VIS-NIR) spectroscopy combined with chemometrics was investigated for fast determination of soluble solids content (SSC) of tea beverage. In this study, a total of 120 tea samples with SSC range of 4.0-9.5 ºBrix were tested. Samples were randomly divided for calibration (n=90) and independent validation (n=30). Spectra were collected by a mobile fiber-type UV-VIS-NIR spectrophotometer in transmission mode with recorded wavelength range of 203.64-1128.05 nm. Various calibration approaches, i.e., principal components analysis (PCA), partial least squares (PLS) regression, least squares support vector machine (LSSVM) and back propagation artificial neural network (BPANN), were investigated. The combinations of PCA-BPANN, PCA-LSSVM, PLS-BPANN and PLS-LSSVM were also investigated to build calibration models. Validation results indicated that all these investigated models achieved high prediction accuracy. Especially, PLS-LSSVM achieved best performance with mean coefficient of determination (R2) of 0.99, root-mean-square error of prediction (RMSEP) of 0.12 and residual prediction deviation (RPD) of 15.16. This experiment suggests that it is feasible to measure SSC of tea beverage using UV-VIS-NIR spectroscopy coupled with appropriate multivariate calibration, which may allow using the proposed method for off-line and on-line quality supervision in the production of soft drink.


2020 ◽  
Vol 2020 ◽  
pp. 1-9
Author(s):  
Mohd Yusop Nurida ◽  
Dolmat Norfadilah ◽  
Mohd Rozaiddin Siti Aishah ◽  
Chan Zhe Phak ◽  
Syafiqa M. Saleh

The analytical methods for the determination of the amine solvent properties do not provide input data for real-time process control and optimization and are labor-intensive, time-consuming, and impractical for studies of dynamic changes in a process. In this study, the potential of nondestructive determination of amine concentration, CO2 loading, and water content in CO2 absorption solvent in the gas processing unit was investigated through Fourier transform near-infrared (FT-NIR) spectroscopy that has the ability to readily carry out multicomponent analysis in association with multivariate analysis methods. The FT-NIR spectra for the solvent were captured and interpreted by using suitable spectra wavenumber regions through multivariate statistical techniques such as partial least square (PLS). The calibration model developed for amine determination had the highest coefficient of determination (R2) of 0.9955 and RMSECV of 0.75%. CO2 calibration model achieved R2 of 0.9902 with RMSECV of 0.25% whereas the water calibration model had R2 of 0.9915 with RMSECV of 1.02%. The statistical evaluation of the validation samples also confirmed that the difference between the actual value and the predicted value from the calibration model was not significantly different and acceptable. Therefore, the amine, CO2, and water models have given a satisfactory result for the concentration determination using the FT-NIR technique. The results of this study indicated that FT-NIR spectroscopy with chemometrics and multivariate technique can be used for the CO2 solvent monitoring to replace the time-consuming and labor-intensive conventional methods.


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