MOSFET power loss characterization: Evolving into multivariate response surface

Author(s):  
Federico Luchino ◽  
Martin Ordonez ◽  
German G. Oggier ◽  
John E. Quaicoe
Molecules ◽  
2020 ◽  
Vol 25 (4) ◽  
pp. 1012
Author(s):  
Teshome Tolcha ◽  
Tura Gemechu ◽  
Said Al-Hamimi ◽  
Negussie Megersa ◽  
Charlotta Turner

The excessive use of pesticides is a serious health problem due to their toxicity and bioaccumulation through the food chain. Due to the complexity of foods, the analysis of pesticides is challenging often giving large matrix effects and co-extracted compounds. To overcome this problem, a selective and “green” supercritical fluid extraction method was developed, using neat carbon dioxide as a solvent at pressures of up to 800 bars. A Box–Behnken response surface experimental design was used, with the independent variables of density (0.70−1.0 g mL−1), temperature (40−70 °C), and volume (10−40 mL) of solvent, and the dependent variable of extracted amount of pesticides. The optimum extraction condition was found at the use of 29 mL of supercritical CO2 at 0.90 g mL−1 and 53 °C (corresponding to 372 bars of pressure). It was observed that increasing the density of CO2 significantly increased the extraction recovery of endrin and 2,4′-dichlorodiphenyldichloroethane. Matrix-matched calibration curves showed satisfactory linearity (R2 ≥ 0.994), and LODs ranged from 0.2 to 2.0 ng g−1. Precision was lower than 11% and recoveries between 80%–103%. Thus, the developed method could efficiently be used for trace analysis of pesticides in complex food matrices without the use of organic solvents.


1981 ◽  
Author(s):  
G E Siefring ◽  
J A Wehrly

A fully automated method for the determination of functional fibrinogen has been developed for the Du Pont ‘aca’. The basis of the assay is the measurement of turbidity formation upon the addition of thrombin to the test plasma. The method can measure fibrinogen in the plasma of patients on heparin therapy and provides a stat result in eight minutes.The assay of fibrinogen is accomplished in a two-stage sequence. First, clot enhancing agents and a heparin neutralizing compound are added. Thrombin is added in the second step to catalyze fibrin formation, the rate of turbidity change being proportional to the fibrinogen concentration. Optimization of the assay under ‘aca’ conditions was accomplished through the use of multivariate response surface analysis. The analytical performance of the method was judged to be acceptable based on precision, interference, and correlation studies. The range of the method is 40-1000 mg/dl fibrinogen. This ‘aca’ method represents the first fully automated determination of functional fibrinogen.


1988 ◽  
Vol 34 (5) ◽  
pp. 954-957 ◽  
Author(s):  
C Flandrois ◽  
C Lahet ◽  
D Feldmann ◽  
J M Gabastou ◽  
A Gonnon ◽  
...  

Abstract Optimization of determination of alanine aminopeptidase in urine by univariate study led to a method involving pretreatment of urine with Sephadex G50. Re-examination of the optimization by multivariate study led us to recommend higher optimal concentrations: 5.8 mmol/L for the substrate and 300 mmol/L for the Tris buffer. Under these new conditions, pretreatment of urine was no longer necessary and the assay could be completely automated.


Sign in / Sign up

Export Citation Format

Share Document