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iodide
The determination limit of iodide is 2 × 10-4 μg/mL.
      
It was demonstrated that the reactions with iodide at pH 5-10 and with thiosulfate at pH 10 are significant in the determination of lead as three-component complexes on the support.
      
The selectivity coefficients of the electrodes under study to chloride and iodide ions were determined.
      
Semiconductor sensing elements based on iodide-doped lead sulfide were developed for determining nitrogen oxides (NO, NO2).
      
Potentiometric Determination of Mercury with Iodide-Selective Electrodes
      
The conditions for the application of commercial Radelkis OR-I-7111-D (Hungary) and Crytur 53-17 (Czech Republic) iodide-selective electrodes to the determination of mercury were found.
      
Catalytic Titrations of Silver(I) Using an Iodide-Catalyzed Mn(IV)-As(III) Indicator Reaction in the Presence of Sulfuric Acid w
      
Catalytic bipotentiometric and biamperometric methods for determining silver(I) with the use of the new manganese(IV)-arsenic(III) indicator reaction catalyzed by iodide ions in the presence of sulfuric acid have been developed.
      
The electrochemical behavior of Crystal Violet (CV) on the surface of a glassy carbon electrode in potassium chloride, nitrate, and iodide supporting electrolytes was studied using stripping voltammetry.
      
This property can be used for determining iodide by adsorption-stripping voltammetry.
      
The excess periodate that is related to the amount of catecholamines is determined by its reaction with iodide in the presence of methylene blue.
      
The analytical signals in the sorption and determination of Cd, Pb, and Hg with dithizone and PAR on the solid phase were maximum for iodide and thiosulfate complexes.
      
The method is based on passing the mixture before absorption with a potassium iodide solution through a furnace, where the ozone is decomposed.
      
The sorption of mercury as chloride, iodide, sulfate, thiosulfate, nitrate, and EDTA complexes was studied.
      
Electrochemical Preconcentration of Iodide and Its Determination by Cathodic Stripping Voltammetry
      
The results obtained were used for determining iodide by cathodic stripping voltammetry in the concentration range of 6 to 500 μg/L.
      
The detection limit for iodide was found to be 0.2 μg/L at an electrolysis time of 3 min.
      
Kinetic Determination of Iodide by the Sandell-Kolthoff Reaction Using Diphenylamine-4-Sulfonic Acid
      
A mixture of dithizone with EDTA, acetate, iodide, or thiosulfate can be used for masking concomitant elements.
      
Effect of Lactic Acid on the Electrochemical Determination of Iodide Ions
      
 

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