Optical chemical sensor of Gd(iii) based on 5-(2'-bromophenyl- azo)-6-hydroxypyrimidine-2,4-dione immobilized on poly(methyl methacrylate) and 2-nitrophenyloctylether matrix.

A novel optical chemical sensor (optode) was fabricated for the determination of Gadolinium ions. The optical sensor was prepared by incorporating a recently synthesized ionophore, 5-(2'-bromophenylazo)-6-hydroxy pyrimidine-2,4-dione (BPAHPD), and 2-nitrophenyloctylether (NPOE) as a plasticizer in poly(methyl methacrylate) (PMMA) membrane. The color of the sensing membrane in contact with Gd(iii) ions changed from yellow to red-orange due to the adsorption of Gd(iii) with the maximum absorbance (λ max) at 563 nm. The chemical sensor responds optimally towards Gd(iii) ions at the optimum conditions of pH 7.5, contact time 10 min, 150 ng mL-1 Gd(iii), and 5.0 mL solution. The linear regression equation achieved was A = 4.36C (µg mL-1) - 0.15 (r = 0.9976). A linear Gd(iii) calibration curve can be established in the concentration range of 5.0-250 ng mL-1 with R 2 = 0.9976. Detection and quantification limits are 1.47 and 4.75 ng mL-1, respectively. The molar absorptivity and Sandell sensitivity are found to be 6.86 × 107 L mol-1 cm-1 and 0.023 ng cm-2, respectively. In addition to its stability and reproducibility, the optode revealed a great selectivity toward Gd(iii) ions as compared to other coexisting ions in real samples. The recovery of Gd(iii) ions from the sensor material was achieved using 0.4 M HNO3 . The offered optode sensor membrane has been employed to monitor Gd(iii) in soil, sediments, river water, and urine with an internal standard addition method and compared statistically with the ICP-OES method. The results revealed calculated t-values between 1.11-1.85, whereas F values were in the range of 2.46-3.77 which did not exceed the theoretical values, indicating no significant difference at 95% confidence level. The observed percent recovery is in the range of 97.24-102.52%.

A highly selective bulk optode based on 6-{4-(2,4-dihydroxy-phenyl)diazenyl)phenyl}-2-oxo-4-phenyl-1,2-dihydro-pyridine-3-carbonitrile incorporating chromoionophore V for determination of nano levels of cadmium.

A novel optical sensor has been fabricated for highly accurate, simple and selective determination of nanomolar levels of cadmium ions. The sensor depends on the interaction of 6-{4-(2,4-dihydroxyphenyl)diazenyl)phenyl}-2-oxo-4-phenyl-1,2-dihydropyri-dine-3-carbonitrile (DDPODC) with Cd(II) in plasticized (2-nitrophenyloctyl ether) (o-NPOE) polyvinylchloride (PVC) membrane incorporating chromoionophore V as a lipophilic H+-selective indicator. It would seem that the higher Cd(II) concentration, the lower absorbance of chromoionophore V in the membrane at 668 nm, whereas the absorbance at 586 nm increased. The developed sensor at pH 4.7 has a linear range of 5.0 × 10-12 - 2.5 × 10-5 M with limits of detection and quantification of 1.62 × 10-12 and 4.95 × 10-12 M, respectively. The relative standard deviation (RSD) for eight determination of 1.0 × 10-7 M Cd(II) was 1.67%. Finally, the proposed sensor gives good results for applications in the direct determination of cadmium ions in water, food, and biological samples. Additionally, we compared the obtained results with the data obtained from the flame atomic absorption spectrometry (FAAS).

Utilization of a plasticized PVC optical sensor for the selective and efficient detection of cobalt(ii) in environmental samples.

A novel sensitive, selective, and reversible cobalt(ii) ion optical sensor was prepared by the incorporation of 5-[o-carboxyphenylazo]2,4-dihydroxybenzoic acid [CPDB] and sodium tetraphenylborate (NaTPB) in a plasticized polyvinyl chloride (PVC) membrane containing dioctyl adipate (DOA) as a plasticizer. The influence of several parameters such as pH, base matrix, solvent mediator and reagent concentration was optimized. A comparison of the obtained results with those of previously reported sensors revealed that the proposed method, in addition to being fast and simple, provided a good linear range (0.05-45.20 µM) and low detection limit (0.015 µM). Low detection and quantification limits and excellent selectivity in the presence of interfering ions such as Fe3+, Cu2+, Ni2+, Ag+, Au3+, Cr3+, Cd2+, Zn2+, Hg2+, and SO4 2- make it feasible to monitor Co2+ ion content accurately and repeatedly in environmental samples with complicated matrices. The optode was regenerated successfully using 0.3 M nitric acid (HNO3) solution while its response was reversible with a relative standard deviation (RSD) lower than 1.9% for seven replicate determinations of 20 µM Co2+ in various membranes. The optode was stable and was stored for at least 15 days without observing any change in its sensitivity.