Kappa-carrageenan for benign preparation of CdSeNPs enhancing the electrochemical measurement of AC symmetric supercapacitor device based on neutral aqueous electrolyte.

This study presents the development of an electrochemical supercapacitor with a cadmium selenide nanoparticles (CdSeNPs) electrode utilizing a straightforward and economical method based on kappa-carrageenan (κ-CGN). The structural, morphological, and optical characteristics of CdSeNPs were assessed. Activated carbon (AC) and green-prepared CdSeNPs were easily mixed to achieve excellent electrochemical properties. The nanoelectrode (AC@CdSe) was tested in an aqueous electrolyte of sodium sulfate (Na2SO4) with a concentration of 1 Molar. Specific capacitance (Csp) for the AC electrode and the AC@CdSe electrode at 1 A g-1 was calculated to be 103 and 480 F g-1, respectively. Besides, the symmetric supercapacitor AC@CdSe/AC@CdSe device has a high specific energy of 52 Wh kg-1 and a maximum specific power of 2880 W kg-1, with a specific capacitance of 115.5 F g-1. With a coulombic efficiency of between 82 % and 100 %, the device continues to maintain excellent capacitance after 10.000 cycles.

Polymeric Electrochemical Sensor for Calcium Based on DNA.

Plastic membranes containing deoxyribonucleic acid (DNA) as an electroactive material were acting as Ca2+ selective sensors. Diethyl phthalate (DEP), dioctyl Phthalate (DOP), or nitrophenyl octyl ether (NPOE) were used as plasticizers and polyvinyl chloride (PVC) was the membrane matrix. A sensor with a membrane composition of 120 mg PVC, 60 mg DOP plasticizer, and 2 mg DNA ionophore (DNA: DOP: PVC, 1.0:29.2:0.1 mole) was found to have the best performance. The slope of the calibration graph was 30 mV decade-1. The optimum pH range was 5.7-9.5 for 0.01 M Ca2+. The sensor response time was fast (2-3 s) with a long working period (up to 3 weeks). Excellent selectivity for Ca2+ was indicated by the values of selectivity coefficients for different selected interference. The sensor was used effectively for the estimation of calcium in real samples (fruits, calcium syrup, milk, and dairy products).

Blank membranes versus ionophore-based membranes for the selective determination of H+.

A pH electrode for the selective determination of H+ was introduced. Both phosphorated calix[6]arene and a N,N'-bisethoxycarbonyl-1,10-diaza-4,7,13,16-tetraoxacyclo-octadecane (DZCE) were used as new H+-ionophores. The calibration graphs of the obtained electrodes exhibits satisfactory Nernstian slopes. The electrodes were compared to blank membranes (without any ionophoric substances) for the first time. Selectivity coefficients of the studied electrodes towards several inorganic cations were calculated. The relative selectivity coefficient (RSC) was applied for evaluating the selectivity properties of H+-electrode using a mathematical equation. The electrodes were applied for the determination of different inorganic and organic acids.

Atropine-selective membrane electrodes and relative selectivity concept.

TFPB was introduced as a charged ionophore for atropine selective electrodes. Typical Nernstian responses were found (57.78, 58.95 and 58.41 mV/decade) for PVC-membrane electrodes incorporating NPOE, DOS, and DDP as plasticizers. They exhibited practical linear ranges of 9.1 x 10(-3) - 10(-6), 9.1 x 10(-3) - 10(-6) and 9.1 x 10(-3) - 10(-7) M, respectively. It works in the sub-micro scale of atropine concentrations. The optimum pH-range was 3.18 - 8.97. The selectivity coefficient values were estimated for different organic and inorganic cations. They were interpreted by using the "Relative Selectivity Concept", which was introduced for the first time. The new concept was applied for comparing the selectivity properties of previously reported electrodes. The effect of the presence of ephedrine, caffeine, glucose, Na(+), Ca(2+), and Mg(2+) on the calibration graphs of the electrodes was studied.

Phosphorated calix[6]arene derivatives as an ionophore for atropine-selective membrane electrodes.

37,40-bis-[(diethoxy-thiophosphoryl)oxy]-5,11,17, 23,29,35-hexakis(1,1 -dimethyl-ethyl)-calix[6]arene-8,39,41,42-tetrol; 37,38,39,40,41-pentakis-(di-ethoxythiophosphoryl)-oxy]-5,11,17,23,29,35-hexakis (1,1-dimethylethyl)-calix[6]-arene-42-ol; and 37-[(diethoxythiophosphoryl)oxy]-5,11,17,23,29,35-hexakis-(1,1dimethylethyl)-calix[6]arene-38,39,40, 41,42-pentol were introduced as neutral ionophores for atropine-selective electrodes. Practical Nernstian responses were found (54.3, 49.1, and 50.8 mV/decade) for polyvinyl chloride membrane electrodes incorporating these compounds. They exhibited practical linear ranges of 1.9 x 10(-6)-7.9 x 10(-3), 7.9 x 10(-6)-7.9 x 10(-3), and 6.3 x 10(-6)-7.9 x 10(-3) M, respectively. The optimum pH range was 2.5-8.5. The selectivity coefficient values were estimated and interpreted. The electrode performance was correlated to the calixarene structure. Then, the electrode was applied to an actual analysis of pharmaceutical atropine preparations. The recovery values of 18.7 microg/mL-5.5193 mg/mL atropine sulfate were 97.5-99.1%. The corresponding relative standard deviation values ranged between 0.39-0.72% for 5 determinations. The first electrode was applied successfully for analyzing atropine sulfate in injection solution and eye drops.