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However, a similar dependence of respiration in state 4 is linear over the whole temperature range and corresponds to the activation energy of 17 kJ/mol.
      
The calibration curve is linear over the concentration range 2.0-100 Μg of nickel in 5 mL of the final dimethylformamide solution.
      
For linear sweep, calibration plots were linear over the entire concentration range for all signal-processing methods.
      
The calibration graph was linear over the range of 0.050-1.20 μg/mL, with a limit of detection of 0.03 μg/mL.
      
The Stern-Volmer relationships for phosphorescence quenching are linear over the entire range of oxygen concentrations.
      
The calibration graph was linear over the range 0.1-2.0 mg/L with a detection limit of 0.03 mg/L and a precision of 0.5%.
      
The calibration plot was linear over the range 0.1-20 μg/L at an accumulation time of 10 s.
      
The calibration graph was linear over the concentration range 1-20 ng/mL; the detection limit for nonylphenol was 0.8 ng/mL.
      
The calibration graph was linear over the range (2-10) × 10-7 M (r2 = 0.9985) with relative standard deviations (n = 5) in the range 1.0-2.3%.
      
The calibration curve is linear over the range 0.1 to 5.0 μg/mL of palladium(II) in the final solution with a correlation coefficient of 0.9996.
      
The current response was linear over two orders of magnitude with detection limits (S/N = 3) ranging from 6.00 × 10-8 to 3.75 × 10-7 g/mL for all analytes.
      
With the aid of mixed linear Ω-algebras we prove a theorem to the effect that the cancellation law is satisfied in a groupoid of subvarieties of a variety of Ω-algebras linear over a field and given by identities of zero order.
      
We show that in some varieties of Ω-algebras linear over an infinite ring of principal ideals there are no nontrivial finitely attainable subvarieties.
      
In the case of anticommutative rings (Ω-rings) this property holds for Ω-algebras, linear over an arbitrary integral domain without stable ideals.
      
It is demonstrated that an increase in the amplitude of vibrations results in an increase in the effective mass transfer coefficient, with its dependence on the squared amplitude being linear over the range covered.
      
We perfused hindlimbs from Sprague-Dawley rats with ANG I and observed ANG II production, which was linear over a 10000-fold concentration range of ANG I.
      
The response of detectors is not linear over a very large range, and any deviation from linearity results in a systematic error in the determination of the peak area and of its moments.
      
The detection limit for carbon is 500 ng or less, and the response is linear over at least two decades.
      
The ΔCd-analyte concentration response curves are linear over a limited range.
      
Calibration curves were linear over the entire concentration range 5-100 ng/ml for cyclizine in serum and urine and for norcyclizine in urine.
      
 

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