RU95116229A -
METHOD FOR POTENTIOMETRIC DETERMINATION OF SUBSTANCE CONCENTRATION
- Google Patents
METHOD FOR POTENTIOMETRIC DETERMINATION OF SUBSTANCE CONCENTRATION
Info
Publication number
RU95116229A
RU95116229ARU95116229/25ARU95116229ARU95116229ARU 95116229 ARU95116229 ARU 95116229ARU 95116229/25 ARU95116229/25 ARU 95116229/25ARU 95116229 ARU95116229 ARU 95116229ARU 95116229 ARU95116229 ARU 95116229A
Способ потенциометрического определения концентрации веществ в растворах экстракционных систем, отличающийся тем, что измеряют скачок потенциала в органической фазе, осуществляя токоотвод через контактирующие с ней водные фазы, одна из которых является стандартным, а другая - испытуемым растворами, и определяют концентрацию по градуировочному графику в координатах "скачок потенциала - концентрация испытуемого раствора".A method for potentiometric determination of the concentration of substances in solutions of extraction systems, characterized in that they measure the potential jump in the organic phase by conducting a current drain through the aqueous phases in contact with it, one of which is standard and the other with test solutions, and determine the concentration according to the calibration curve in coordinates "potential jump - concentration of the test solution."
RU95116229A1995-09-191995-09-19Method of potentiometer determination of substance concentration
RU2092829C1
(en)
Combining poly (methacrylic acid-co-ethylene glycol dimethacrylate) monolith microextraction and on-line pre-concentration-capillary electrophoresis for analysis of ephedrine and pseudoephedrine in human plasma and urine
Fast determination of diphenhydramine, pyridoxine, and 8-chlorotheophylline by capillary electrophoresis with capacitively coupled contactless conductivity detection
Indirect voltammetric sensing platforms for fluoride detection on boron-doped diamond electrode mediated via [FeF6] 3− and [CeF6] 2− complexes formation
Improved method for measuring the glycine and taurine conjugates of bile salts by high-performance liquid chromatography with tauro-7 alpha, 12 alpha-dihydroxy-5 beta-cholanic acid as internal standard