Examples of using Linear range in English and their translations into Portuguese
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Its linear range is 0 to 20 ppm.
Influence of ride frequencies in vehicle comfort and stability at linear range of….
The linear range for determination of cr by wc aes was 10- 100¿g l-1.
Chemiluminescent methods are known by high sensitivity and wide linear range for analytes detection.
For eto a linear range from 1.0 to 80.0¿mol l¿1 was obtained with lod and loq equal to 0.294 and 0.980¿mol l¿1, respectively.
They showed results similar to the tests in flexural behavior for loads in the linear range, but different values for a nonlinear analysis.
Good linear ranges were obtained for the respective analytical curves with values of 0.60 to 50.0^mol l-1 for ivm and 0.01 to.
The numerical techniques used to evaluate the behavior of linear systems and to establish the linear range will be addressed in the text below.
The linear range was 1.00 to 40.0 mg l-1, the limit of detection(ld) was 0.43 mg l-1and the limit of quantification(lq) was 1.32 mg l-1.
Differential pulse voltammetry detected a linear range of ca125 target, from 0 to 80 u. ml-1, with detection limit of 1,45 u. ml-1.
To do so, sixteen sulfur compounds were studied in different oxidation states(¿ii,+ii,+iv),obtaining the linear range and detection limit for each compound.
The fluorescence method had linear range from 0.30 to 0.60 mg l-1, limit of quantification of 0.27 mg l-1 and limit of detection of 0.11 mg l-1.
Keywords experimental data, calibration curve, analytical techniques, linear regression, numerical techniques,linear structures, linear range.
After the optimized solvent afforded an analytical curve with a linear range of concentration ranging between clotrimazole 2.95 x10-5 to 5.90¿10-4 mol l- 1.
The linear range of the method and the linearity of the calibration curves prepared in the solvents and in the matrices were determined by studying the matrix effects.
The square wave voltammetry was used to construct the calibration curves,obtaining linear range of 4.9¿10-7- 2.9¿10-5 mol l-1 for anl and 1.9¿10-5- 2.8¿10-4 mol l-1 to val in binary mi.
The different linear ranges were selected from univariate models, and verified using tests of lack of fit and significance by the anova(analysis of variance) study.
Even to say that opinions run from one extreme to the other would be misleading,in that it would falsely imply a linear range where there is instead a multidimensional scattering.
Regarding hydrogen peroxide method the parameters were: linear range from 0.2 to 1.4 mmol l-1(r= 0.999) and detection limits(lod) and quantification(loq) of 12.5¿mol l-1 and 41.7¿mol l-1.
The determination of linuron in natural water samples andcommercial products was successfully performed using the boron doped diamond with good linear range, repeatability, sensitivity and stability.
A constant sum of the secondaries, throughout the linear range, insures compatibility with ratiometric temperature compensation signal conditioning schemes.
For the determination of tbz, 60 min uv irradiation of the analyte prepared in naoh(0.45 mol l-1) allowed its quantification by spectrofluorimetry with a limit of detection(lod)of 1.4 x 10-8 mol l-1 and a linear range extending up to 1 x 10-5 mol l-1.
The procedure showed a linear range varying between 5.55x10-5 to 3.33x10-4 mol l-1 for quantification of bha. the linear range for bht determination varying between 9.08x10-5 to 5.44x10-4 mol l-1.
Under the optimum working conditions(mcllvaine buffer 0.1 mol l-1, ph 3.5),the calibration curve showed a linear range of 0,9 to 19,6¿mol l- 1 for both electrodes, with detection limits of 0,5 and 0,4¿mol l-1, respectively.
The cmes were applied as sensors for the electroanalysis of biologically important antioxidants. it was possible to successfully determine ascorbic acid(dl 0.19 mmol. l-1) in the presence of uric acid, cysteine(dl 8.25 nmol. l-1) and homocysteine(dl 0.6 mmol. l-1)which showed excellent limits of detection and quantification, sensitivity and linear range.
If the elastic response spectrum intersects the linear range of the capacity spectrum, this point is called the Performance Point and represents the maximum displacement of the structure submitted to the proposed action.
In the second one, has been used a glassy carbon electrode modified with a mercury film, andthe supported electrolyte was used kcl 0.1 mol l-1. the calibration curve was linear range of 80 to 800¿g l-1 with a correlation coefficient r2 0.997.
The method presents the following analytical features: linear range from 0.17 to 6.0¿g l -1, limit of detection and quantification of 53 and 170 ng l -1, respectively, of preconcentration factor of 232 and reading frequency analysis of 12 h -1; which were all applied in food samples.
With the electroactive enzymatic products obtained from p-aminophenyl phosphate, hydroquinone diphosphate, and phosphorylated paracetamol, you can achieve simple electrochemical detection while increasing sensitivity andgetting wider linear ranges than would be obtained with other standard AP substrates.
The developed method was applied to hydroquinone determination andfurnished the following analytical parameters: linear range 0 to 120.0¿mol l-1(r= 0.996) and limits of detection(lod) and quantification(loq) were obtained 0.78¿mol l-1 and 2.60¿mol l-1, respectively.