1c:I[419806,["/_next/static/chunks/bb923814e1f4d2e9.js","/_next/static/chunks/dd3ee9f5b7716ca6.js","/_next/static/chunks/4204a0ae82542ca8.js","/_next/static/chunks/30036bedc5269936.js","/_next/static/chunks/6e1aa89a642f40be.js","/_next/static/chunks/cd5e572bc3e4eb92.js","/_next/static/chunks/8ffd0b71567920d8.js","/_next/static/chunks/67ea6dfd21f16c5f.js","/_next/static/chunks/24eb4379f68013fd.js","/_next/static/chunks/b8cd775ffdf935bd.js","/_next/static/chunks/983103cd9eb7b428.js","/_next/static/chunks/d4ac9dcf27f6ff52.js","/_next/static/chunks/294b9525248c8e5f.js"],"default"] 1d:T55e,Poly(vinyl chloride) (PVC) based membranes of macrocycles, 5,7,7,12,14,14-hexamethyl-1,4,8,11- tetraazacyclotetradeca-4,11-diene diperchlorate (I), 3,5,7,7,10,12,14,14-octamethyl-1,4,8,11-tetraazacyclo- tetradeca-4,11-diene diperchlorate (II) and 5,10,15,20-tetraphenylporphyrin(III) with sodium tetraphenylborate (STB) as an anion excluder and dibutyl phthalate (DBP), dioctyl phthalate (DOP), dibutyl butylphosphonate (DBBP) and 1-chloronaphthalene (CN) as plasticizing solvent mediators were prepared and investigated as Co 2 + -selective electrodes. The best performance was observed with the membrane having the composition III–PVC–STB–DBP in the ratio 3:8:1:8, which works well over a wide concentration range (8.0 × 10 - 6 –1.0 × 10 - 1 mol l -1 ) with a Nernstian slope of 29.0 mV per decade of activity between pH 2.8 and 7.3. This electrode shows a fast response time of 20 s and was used over a period of 4 months with good reproducibility (s = 0.4 mV). The selectivity coefficient values of the order of 0.01 for mono-, di- and trivalent cations indicate excellent selectivity for Co 2 + over a large number of cations. Anions such as Cl - and SO 4 2 - do not interfere and the electrode also works satisfactorily in a partially non-aqueous medium. The sensor has been used as an indicator electrode in the potentiometric titration of Co 2 + with EDTA.1e:T429,The electrochemical behavior of indigo carmine (IC) at poly (glycine) modified carbon paste electrode (PGMCPE) was investigated by cyclic and differential pulse voltammetry. The oxidation peak of IC was observed in phosphate buffer of pH 6.5. The influence of different pH, scan rate, and concentration were analyzed. The probable reaction mechanism involved in the oxidation of IC was also proposed. Results showed that PGMCPE a remarkable electrocatalytic activity for the oxidation of IC under optimal conditions. The electrocatalytic response of the sensor was proportional to the IC concentration in the range of (2 × 10^-6-1 × 10^-5 M) and (1.5 × 10^-5-6 × 10^-5 M) with a limit of detection 11 × 10^-8 M and limit of quantification 3.6 × 10^-7 M. The modified electrode demonstrated many advantages such as simple preparation, high sensitivity, low detection of limit, excellent catalytic activity, short response time, and remarkable antifouling property toward IC and its oxidation product.

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