Ece Kök Yetimoğlu

Removal of Lead and Cadmium Ions from Aqueous Solutions Using Sulphur and Oxygen Donor Ligand Bearing Hydrogels

A new thiourea and urea functional monomers were synthesized. A series of hydrogels were prepared by photopolymerization. The hydrogels were used for the removal of Pb(II) and Cd(II) ions from aqueous solutions. The influence of the uptake conditions such as the pH, the time, and the initial feed concentration on the metal ion binding capacity of hydrogel was tested. The selectivity of the hydrogels towards the different metal ions was also tested. The adsorption isotherm models were applied. The limits of detection and quantification were calculated. The usability of the hydrogels for preconcentration studies were also investigated.

Adsorption of Ag (I) Ions from Aqueous Solutions Using Photocured Thiol-Ene Hydrogel

In this present work, we reported the adsorption and recovery studies of a P(Penta3MP4/PEG-DA/HEMA) thiol-ene based hydrogel. Real-time infrared spectroscopy technique was used to identify the photopolymerization kinetics of thiol-ene based formulations. The chemical composition and surface morphology of hydrogels were also characterized. The influence of the adsorption conditions such as pH, hydrogel formulations, contact time, initial metal ion concentration, and foreign metal ions on the metal ion binding capacity of hydrogel, were tested. Both the Langmuir and Freundlich isotherm models were applied to the method. The reusability of the hydrogels and the usability of the hydrogels for preconcentration studies were also investigated. The analytical parameters of the method were calculated and the recovery of silver ions from waste radiographic films was also applied to the hydrogels.

Uptake of Pb2+ Using N-Vinyl Imidazole Based Uniform Porous Hydrogels

The uniform porous and continuous phase lead (II) adsorbent hydrogel, was prepared by copolymerizing 2-hydroxyethyl methacrylate (HEMA), acrylic acid (AAc), and N,N′-methylenebisacrylamide (MBAAm), with n-vinyl imidazole (VIM). A series of hydrogels, including different ratios of VIM, were prepared by photopolymerization and characterized. The influence of the uptake conditions such as pH, functional monomer percent, contact time, initial feed concentration, and foreign metal ions on the metal ion binding capacity of hydrogel, were also tested. The selective chelation of heavy metal ions from synthetic wastewater was also studied. The affinity order on molar basis was observed as follows: Pb (II) > Zn (II) > Cd (II). Chelation behavior of heavy metal ions could be modelled using both the Langmuir and Freundlich isotherms and it was seen that the Langmuir isotherm model was the best fit for the adsorption of Pb (II) ions in P(VIM/AAc/HEMA) hydrogel. Moreover, the limits of detection and the quantification values were determined. Regeneration of the hydrogels was easily performed with 1 M HCl and the same hydrogel can be reused five times almost without any loss of adsorption capacity. All these features make P(VIM/AAc/HEMA) hydrogels potential candidate adsorbent for heavy metal removal.

Multivariate analysis of metal contamination in street dusts of Istanbul D-100 highway

Metals are found in street dust especially in big cities, like Istanbul. This is a significant contribution to the environmental pollution. For this purpose, fifty six samples of Istanbul street dust were collected for metal contamination analysis in the period of December 2003 to April 2004. The mean concentration of Pb, Zn, Ni, Cd and Cu determined by graphite furnace atomic absorption spectrometry were found to be 368.3, 431.2, 27.1, 0.3 and 191.1 µg g-1 respectively. Metal values in street dust samples were several times higher than the control. Correlations among the different metal concentrations were calculated. Multivariate statistical analyses (principal component analysis - PCA and cluster analysis - CA) were applied to the data matrix to determine the analytical results and to identify the possible origin of metals in these dusts. The results indicate that Pb, Zn, Cd, Ni and Cu are mainly originated from anthropogenic sources.

Removal of Ag(I) from Aqueous Solutions by Thiol-ene-Based Hydrogel and Its Application to Radiographic Films

The thiol-ene-based P(Penta3MP4/PEGDA/AAc) hydrogels were prepared by UV curing technique, then characterized and used as adsorbents for the investigation of the effect of process parameters such as pH of solution, contact time, and initial concentration of solution, on the removal of Ag(I) from aqueous solution. The results indicate that the adsorption of Ag(I) ions from aqueous solutions is strongly dependent on pH under experimental conditions. Both Langmuir and Freundlich isotherm models were applied to experimental data, and the results show that the adsorption process is well fitted to the Langmuir isotherm model. Selectivity, reusability, and applicability of hydrogels to radiographic film waste were investigated.

Solidified Floating Organic Drop Microextraction for the Detection of Trace Amount of Lead in Various Samples by Electrothermal Atomic Absorption Spectrometry

A novel method was developed for determination of trace amounts of lead in water and food samples. Solidified floating organic drop microextraction was used to preconcentrate the lead ion. After the analyte was complexed with 1-(2-pyridylazo)-2-naphthol, undecanol and acetonitrile were added as extraction and dispersive solvent, respectively. Variables such as pH, volumes of extraction and dispersive solvents, and concentration of chelating agent were optimized. Under the optimum conditions, the detection limit of Pb (II) was determined as 0.042 µg L−1 with an enrichment factor of 300. The relative standard deviation is <10%. Accuracy of the developed procedure was evaluated by the analysis of certified reference material of human hair (NCS DC 73347) and wastewater (SPS-WW2) with satisfactory results. The developed procedure was then successfully applied to biscuit and water samples for detection of Pb (II) ions.

Recovery of Au(III) ions by Au(III)-imprinted hydrogel

A new Au(III)-imprinted hydrogel (Au(III)-Imp) was prepared by the photopolymerisation of 4-acryloylmorpholine (AcM), 2-hydroxyethyl acrylate (HEA), and poly(ethylene glycol) diacrylate (cross-linking monomer, PEG-DA) in the presence of gold ions. In addition, non-imprinted hydrogel (N-Imp) was similarly prepared without Au(III) ions The Au(III)-Imp hydrogel was characterised by several techniques. To achieve the optimal conditions, effect of pH, time, and initial metal ion concentrations were investigated using a batch system. The pre-concentration factor for Au(III) ions was found to be at least 100. The analytical parameters of the method were determined and the method was also successfully applied to computer circuit board scrap samples. The reusability of the Au(III)-Imp hydrogel was also determined.

Photocured thiol-ene based optical fluorescence sensor for determination of gold(III).

This study describes the preparation and the characterization of a new thiol-ene based polymeric fluorescence sensor by photo initiated polymerization of trimethylolpropane tris(3-mercaptopropionate), 2-hydroxyethylacrylate, and 2,4,6-triallyloxy-1,3,5-triazine which are used as monomers and also a photo initiator (2,2-dimethoxy-2-phenylacetophenone) for its usage as optical sensor for gold ions. The thiol-ene based polymeric membrane sensor was characterized by using attenuated total reflectance-fourier transform infrared spectroscopy (ATR-FTIR) and scanning electron microscopy (SEM). The response characteristics of the sensors including dynamic range, pH effect, response time, and the effect of foreign ions were investigated. Fluorescence spectra showed that the excitation/emission maxima of the membrane were at 379/425 nm, respectively.

Reusable fluorescent photocrosslinked polymeric sensor for determining lead ions in aqueous media.

In this study, 1-vinylimidazole units bearing photocured films were prepared as fluorescent sensors towards Pb(2+) in aqueous solutions. The influence of experimental parameters such as pH, time and foreign ion concentrations were investigated. Sensor response was linear over a concentration range of 4.83×10(-8) to 4.83×10(-7) mol L(-1). The sensor was highly sensitive with a detection limit as low as 1.87×10(-8)molL(-1), and having a selectivity of over four thousand fold. The response time of the sensor was found to be 5 min. When stored in a desiccator at room temperature the sensor showed good stability after a 5 month period. The fluorescence sensors were successful in the determination of Pb(2+) in water samples as well as in the determination of the quantitative amount of lead and the results were satisfying. Compared with previously reported literature, the prepared new sensor is highly sensitive and selective.