ABSTRACT
The carbon quantum dots (CQDs) have been prepared from medlar seeds with pyrolysis method in an oven at 300 °C. UV-vis absorption spectroscopy, fluorescence spectroscopy, Fourier transform infrared spectroscopy (FTIR) spectroscopy, x-ray diffraction (XRD) technique, x-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM) were used in the characterization of CQDs. CQDs, give a strong blue fluorescence under UV lamp (at 365 nm), have a quantum yield of 12.2%. The influence of metal ions such as K+, Mg2+, Ca2+, Be2+, Cr3+, Mn2+, Ni2+, Ag+, Hg2+, and Al3+ on the fluorescence properties of the CQDs was investigated by means of emission spectrophotometry. CQDs altering fluorescence characteristics depending on the excitation wavelength show selectivity for Hg2+ ions with outstanding fluorescence quenching among the tested metal ions. Based on these results, a new fluorimetric method has been developed for the determination of Hg2+ in real water samples. The linear range of method is 1.0 to 5.0 mgL- 1. Limit of detection and limit of quantification are 0.26 and 0.79 mgL- 1, respectively. The proposed method has been successfully used in determination of Hg2+ ions in tap, sea, and stream water samples with application of addition-recovery experiments.
ABSTRACT
Four fluorescent Schiff bases carrying dipicolylamine groups were designed and synthesized to determine their ion sensor properties in partial aqueous solution. The corresponding amine compound and the aldehyde compounds such as 1-naphthaldehyde, 9-anthraldehyde, phenanthrene-9-carboxaldehyde and 1-pyrenecarboxaldehyde were used to prepare the new Schiff bases. The influence of many metal cations and anions on the spectroscopic properties of the ligands was investigated in ethanol-water (1:1) by means of emission spectrometry. From the spectrofluorimetric titrations, the complexation stoichiometry and complex stability constants of the ligands with Cd2+, Zn2+, Cu2+ and Hg2+ ions were determined. The ligands did not interact with the anions. However, the Schiff base derived from phenanthrene-9-carboxaldehyde showed sensitivity for Cu2+ among the tested metal ions. The phenanthrene-based Schiff base was used as analytical ligand for the simple and fast determination of Cu2+ ion in water samples. A modified standard addition method was used to eliminate matrix effect. The linear range was from 0.3 mg/L to 3.8 µg/L. Detection and quantification limits were 0.14 and 0.43 mg/L, respectively. Maximum contaminant level goal (MCLG) for copper in drinking water according to EPA is 1.3 mg/L. The proposed method has high sensitivity to determine copper in drinking waters.
Subject(s)
Amines/chemistry , Biosensing Techniques/methods , Copper/analysis , Fluorescent Dyes/chemistry , Picolinic Acids/chemistry , Schiff Bases/chemistry , Spectrometry, Fluorescence/methods , Water Pollutants, Chemical/analysisABSTRACT
A chalcone-based Schiff base (5), capable of detecting iron (III) in partially aqueous media, has been designed, then synthesized by the condensation of 3-formyl-2-hydroxyquinoline and acetophenone. To determine iron (III) ion, a simple spectrofluorimetric method was developed by using the synthesized Schiff base. The developed method was validated by analyzing the certified reference material (CRM-SA-C Sandy Soil C). During the process of the determination of iron in food samples, satisfactory accuracy was obtained for spinach and rocket. Nitric acid and hydrogen fluoride were used for the digestion of the certified reference material whereas only nitric acid was used for food samples, in a closed microwave system. Measurements were carried out by using the modified standard addition method. The standard addition graph was linear until 5.0 mg/L. in determination of iron (III). Detection and quantification limits were 0.06 and 0.20 mg/L., respectively. The presented method is simple, time-saving, cost-effective and suitable for determination of iron content of soil and foods.
ABSTRACT
Four new Schiff base ligands carrying naphthalene groups were prepared from the reaction of 2,4-diamino-6-methyl-1,3,5-triazine and 2,4-diamino-6-undecyl-1,3,5-triazine with 2-hydroxy-1-naphthaldehyde. The influence of a series of metal ions including Cu2+, Co2+, Hg2+, Al3+, Cr3+, Fe3+, Pb2+, Ni2+, Cd2+, Zn2+, Mn2+, Ag+, Ba2+, Ca2+ and Mg2+ on the spectroscopic properties of the ligands was investigated by means of absorption and emission spectrometry. The results of spectrophotometric and spectrofluorimetric titrations disclosed the complexation stoichiometry and complex stability constant of the ligands with metal ions. A simple spectrofluorimetric method was developed using the Schiff base derived from 2,4-diamino-6-undecyl-1,3,5-triazine to determine Hg2+ ion. No cleanup or enrichment of the tap water sample was required. A modified standard addition method was used to eliminate matrix effect. The standard addition graph was linear between 0.2 and 2.6 mg/L in determination of Hg2+. Detection and quantification limits were 0.08 and 0.23 mg/L, respectively. The simple and cost-effective method can be applied to water samples.
