Efficient Preconcentration of Cu2+, Zn2+ and Fe3+ with an Agarose-Schiff Base Sorbent

2007 ◽  
Vol 72 (7) ◽  
pp. 908-916 ◽  
Author(s):  
Payman Hashemi ◽  
Hatam Hassanvand ◽  
Hossain Naeimi
Keyword(s):  
Schiff Base ◽  
Metal Ions ◽  
Metal Ion ◽  
Good Accuracy ◽  
Kinetic Studies ◽  
Sample Volume ◽  
Effects Of Ph ◽  
Glass Column ◽  
High Concentrations ◽  
Ph Range

Sorption and preconcentration of Cu2+, Zn2+ and Fe3+ on a salen-type Schiff base, 2,2'- [ethane-1,2-diylbis(nitrilomethylidyne)]bis(2-methylphenol), chemically immobilized on a highly crosslinked agarose support, were studied. Kinetic studies showed higher sorption rates of Cu2+ and Fe3+ in comparison with Zn2+. Half-times (t1/2) of 31, 106 and 58 s were obtained for sorption of Cu2+, Zn2+ and Fe3+ by the sorbent, respectively. Effects of pH, eluent concentration and volume, ionic strength, buffer concentration, sample volume and interferences on the recovery of the metal ions were investigated. A 5-ml portion of 0.4 M HCl solution was sufficient for quantitative elution of the metal ions from 0.5 ml of the sorbent packed in a 6.5 mm i.d. glass column. Quantitative recoveries were obtained in a pH range 5.5-6.5 for all the analytes. The volumes to be concentrated exceeding 500 ml, ionic strengths as high as 0.5 mol l-1, and acetate buffer concentrations up to 0.3 mol l-1 for Zn2+ and 0.4 mol l-1 for Cu2+ and Fe3+ did not have any significant effect on the recoveries. The system tolerated relatively high concentrations of diverse ions. Preconcentration factors up to 100 and detection limits of 0.31, 0.16 and 1.73 μg l-1 were obtained for Cu2+, Zn2+ and Fe3+, respectively, for their determination by a flame AAS instrument. The method was successfully applied to the metal ion determinations in several river water samples with good accuracy.

scholarly journals A Study on the Photocatalytic Reduction of Some Metal Ions in Aqueous Solution Using UV- Titanium Dioxide System

2019 ◽  
pp. 1-7
Author(s):  
I. O. Ekwere ◽  
M. Horsfall ◽  
J. O. E. Otaigbe
Keyword(s):  
Aqueous Solution ◽  
Titanium Dioxide ◽  
Metal Ions ◽  
Metal Ion ◽  
Uv Light ◽  
Kinetic Studies ◽  
Photocatalytic Reduction ◽  
Alkaline Ph ◽  
Removal Of Metal ◽  
Removal Of Metal Ions

The photocatalytic reduction of Cu (II), Pb (II), Cd (II) and Cr (VI) ions in aqueous solution has been investigated. The photocatalyst utilized was nano titanium dioxide, composed of 80% anatase and 20% rutile; the UV light source was a 15 W UV bulb with a wavelength of 254 nm. The results obtained indicated a reduction efficiency order as follows; Cr6+ > Cu2+ > Pb2+ > Cd2+. It was observed that these results correlate with the respective reduction potentials of the metal ions. The effect of pH on the photocatalytic reduction of the metal ions was also carried out and results obtained indicated that with the exception of Cr (VI) ions, higher percentage removal of metal ions from their aqueous solution was recorded at alkaline pH than at acidic pH. This was attributed to an extensive formation of precipitate by the metal ions at alkaline pH. Kinetic studies revealed that the removal of metal ions from their solutions largely followed the pseudo- first-order kinetics. Therefore, the results of this study will be useful in metal ion removal from industrial waste water using photocatalytic process.

scholarly journals Synthesis and Spectral Analysis of Some Metal Ions Complexes with Mixed Ligands of Schiff Base and 1, 10-Phenanthroline

2017 ◽  
Vol 14 (1) ◽  
pp. 135-147
Author(s):  
Baghdad Science Journal
Keyword(s):  
Schiff Base ◽  
Metal Ions ◽  
Metal Complexes ◽  
Mass Spectrometer ◽  
Schiff Base Ligand ◽  
Metal Ion ◽  
Molecular Structures ◽  
Spectroscopic Techniques ◽  
Metal Ion Complexes ◽  
Free Schiff Base

The free Schiff base ligand (HL1) is prepared by being mixed with the co-ligand 1, 10-phenanthroline (L2). The product then is reacted with metal ions: (Cr+3, Fe+3, Co+2, Ni+2, Cu+2 and Cd+2) to get new metal ion complexes. The ligand is prepared and its metal ion complexes are characterized by physic-chemical spectroscopic techniques such as: FT-IR, UV-Vis, spectra, mass spectrometer, molar conductivity, magnetic moment, metal content, chloride content and microanalysis (C.H.N) techniques. The results show the formation of the free Schiff base ligand (HL1). The fragments of the prepared free Schiff base ligand are identified by the mass spectrometer technique. All the analysis of ligand and its metal complexes are in good agreement with the theoretical values indicating the purity of Schiff base ligand and the metal complexes. From the above data, the molecular structures for all the metal complexes are proposed to be octahedral

scholarly journals Effective removal of heavy metal ions from aqueous solutions using a new chelating resin poly [2,5-(1,3,4-thiadiazole)-benzalimine]: kinetic and thermodynamic study

2015 ◽  
Vol 6 (2) ◽  
pp. 310-324 ◽  
Author(s):  
Selvaraj Dinesh Kirupha ◽  
Selvaraj Kalaivani ◽  
Thangaraj Vidhyadevi ◽  
Periyaraman Premkumar ◽  
Palanithamy Baskaralingam ◽  
...  
Keyword(s):  
Metal Ions ◽  
Metal Ion ◽  
Ph Value ◽  
Thermo Gravimetric Analysis ◽  
Kinetic Studies ◽  
Ion Concentration ◽  
Chelating Resin ◽  
Gravimetric Analysis ◽  
Equilibrium Data ◽  
Experimental Values

A novel poly [2,5-(1,3,4-thiadiazole)-benzalimine] abbreviated as TDPI adsorbent was synthesized using simple polycondensation technique. The synthetic route involves the preparation of 2,5-diamino-1,3,4-thiadiazole from 2,5-dithiourea and subsequent condensation with terephthalaldehyde. The resin was chemically characterized using Fourier transform infrared (FT-IR), 1H-NMR, and 13C-NMR spectroscopic analysis. Surface morphology and thermal stability were analyzed using scanning electron microscopy (SEM) and thermo-gravimetric analysis (TGA). The effect of the pH value of solution, contact time, adsorbent dose, and initial metal ion concentration were investigated by batch equilibrium adsorption experiments. Kinetic studies show that the adsorption of metal ions onto the resin proceeds according to the pseudo-second-order model and the equilibrium data were best interpreted by the Redlich–Peterson isotherm. The experimental values of the adsorption capacities of Pb2+, Cu2+, Ni2+, and Cd2+ on to TDPI could reach up to 437.2, 491.6, 493.7, and 481.9 mg.g−1 respectively. The exothermic nature of the process, the affinity of the adsorbent towards the metal ions and the feasibility of the process are explained in the thermodynamic parameters. The resin stability and re-usability studies suggest that the resin is chemically stable (0.3 N HCl and H2SO4) and could be regenerated without any serious decline in performance.

scholarly journals Ion Exchange Properties of a Terpolymer Resin Derived from 2, 4-Dihydroxybenzaldehyde, Oxamide and Formaldehyde

2009 ◽  
Vol 6 (3) ◽  
pp. 639-650 ◽  
Author(s):  
M. V. Tarase ◽  
W. B. Gurnule ◽  
A. B. Zade
Keyword(s):  
Hydrochloric Acid ◽  
Ion Exchange ◽  
Metal Ions ◽  
Metal Ion ◽  
Polymer Sample ◽  
Equilibrium Method ◽  
Wide Ph Range ◽  
Ph Range ◽  
Exchange Properties

Terpolymer resins (2,4-DHBOF) were synthesized by the condensation of 2,4-dihydroxybenzaldehyde and oxamide with formaldehyde in the presence of hydrochloric acid as catalyst, proved to be selective chelation ion exchange terpolymer resins for certain metals. Chelation ion exchange properties of these polymers were studied for Fe+3, Cu+2, Hg+2, Cd+2, Co+2, Zn+2, Ni+2and Pb+2ions. A batch equilibrium method was employed in the study of the selectivity of the distribution of a given metal ions between the polymer sample and a solution containing the metal ion. The study was carried out over a wide pH range and in a media of various ionic strengths. The polymer showed a higher selectivity for Fe+3, Cd+2and Co+2ions than for Cu+2, Hg+2, Zn+2, Ni+2and Pb+2ions.

scholarly journals Trace Metal Detection in Aqueous Reservoirs Using Stilbene Intercalated Layered Rare-Earth Hydroxide Tablets

2020 ◽  
Vol 2020 ◽  
pp. 1-9
Author(s):  
Solomon Omwoma
Keyword(s):  
Trace Metal ◽  
Metal Ions ◽  
Metal Ion ◽  
Aqueous Media ◽  
Mitigation Measures ◽  
Metal Ion Analysis ◽  
Gradual Process ◽  
Metal Detection ◽  
Trace Metal Detection ◽  
High Concentrations

Contamination of aquatic reservoirs with metal ions is a slow gradual process that is not easy to detect. Consequences of the metal ions, especially the ones with high atomic numbers (heavy metals) at high concentrations, are severe and irreversible in aquatic reservoirs. As such, early detection mechanisms, especially at trace concentration, are essential for mitigation measures. In this work, a new, robust, and effective tool for trace metal detection and monitoring in aqueous solutions has been developed. Tablets (1 mm thick and similar to medicinal tablets) were manufactured from a powder comprising stilbene intercalated into gallery spaces of lanthanide-containing layered double hydroxides. The tablets were placed in a water column having different concentrations of Pb2+ and Cu2+ ions, and the water was allowed to flow for 45 minutes at a flow rate of 100 ml/s. Thereafter, the tablets were dried and made to powder, and their phosphorescence was measured. The gradual stilbene phosphorescence turnoff in the tablets from various concentrations of metal ions was correlated with sorption amounts. The tablets were able to detect effectively metal ions (up to Pb2+ 1.0 mmol/L and Cu2+ 5.0 mmol/L) in the aqueous media. As such, the concentrations of Pb2+ and Cu2+ ions at trace levels were determined in the test solutions. This method provides a real-time metal ion analysis and does not involve sampling of water samples for analysis in the laboratory.

Adsorptive removal of lead and cadmium ions from aqueous solutions by aluminium oxide modified onion skin wastes: Adsorbent characterization, equilibrium modelling and kinetic studies

2021 ◽  
pp. 0958305X2198988
Author(s):  
Adeyinka Sikiru Yusuff
Keyword(s):  
Metal Ions ◽  
Contact Time ◽  
Metal Ion ◽  
Aluminium Oxide ◽  
Kinetic Studies ◽  
Process Conditions ◽  
Adsorbent Dosage ◽  
Metal Ion Removal ◽  
Lead And Cadmium ◽  
Onion Skin

Aluminium oxide modified onion skin waste (Al2O3/OSW) was characterized and used for adsorption of metal ions (Pb2+ and Cd2+) in this study, and the relations between sorbent properties and metal ion sorption were investigated. The effects of adsorption process conditions on metal ion removal efficiency, including initial cation concentration, contact time, adsorbent dosage and pH, were examined. The obtained adsorption data were analyzed by various adsorption isotherm and kinetic models. It was found that the optimum values of the initial concentration, contact time, adsorbent dosage and pH were 10 mg/L, 120 min, 1.6 g/L and 6.0, respectively. At these optimum conditions, maximum removal percentages of Pb2+ and Cd2+ were 91.23 and 94.10%, respectively. The isotherm and kinetic studies showed a multilayer adsorbate-adsorbent system with the dominance of the chemisorption mechanism. The study concluded that onion skin waste is a viable, cheap and effective alternative for removing heavy metal ions from water/wastewater.

scholarly journals Design and Development of Complexation of Ce+3 Metal Ions with Synthesized INZ Incorporated Bio-active Schiff Bases

2021 ◽  
Vol 11 (4) ◽  
pp. 3989-4006
Keyword(s):  
Schiff Base ◽  
Metal Ions ◽  
Schiff Bases ◽  
Elemental Analysis ◽  
Metal Ion ◽  
Organic Ligands ◽  
Schiff Base Complexes ◽  
Spectral Techniques ◽  
The Stability ◽  
Antibacterial And Antifungal

In the present research, a series of Ce+3 metal ions complexation with INZ incorporating Schiff bases have been reported. INZ incorporated Schiff Bases (3a-e) were developed by condensing INZ with substituted aromatic aldehyde and confirmed with various spectral Techniques such as Elemental analysis, UV, IR, 1H-NMR, 13H NMR. All the synthesized organic ligands were evaluated against antibacterial and antifungal stains and found moderate to significant results. The Ce+3 metal ion solution mixed with newly prepared bio-active INZ Schiff bases (3a-e) to afford the [Ce-INZ Schiff Base] complexes (4a-e). The stability constants of prepared complexes were evaluated and found in order as a (3e) > (3d) > (3a) > (3b) > (3c).

scholarly journals Nanostructured faujasite zeolite as metal ion adsorbent: kinetics, equilibrium adsorption and metal recovery studies

2020 ◽  
Author(s):  
Mariana B. Goncalves ◽  
Djanyna V. C. Schmidt ◽  
Fabiana S. dos Santos ◽  
Daniel F. Cipriano ◽  
Gustavo R. Gonçalves ◽  
...  
Keyword(s):  
Ion Exchange ◽  
Metal Ions ◽  
Metal Ion ◽  
Active Sites ◽  
Metal Removal ◽  
High Surface ◽  
High Surface Area ◽  
Kinetic Studies ◽  
Crystallization Time ◽  
X Ray

Abstract The hydrothermal synthesis of nano-faujasite has been successfully performed and the effects of some crystallization parameters were investigated, along with the use of this material as a heavy-metal ion adsorbent. X-ray diffraction patterns have shown that the structure of the nano-faujasite is strongly dependent on both the crystallization time and the alkalinity of the synthesis medium. According to N2 physisorption, X-ray fluorescence, SEM/EDS, and solid state 29Si and 27Al NMR data, the produced nano-faujasite consists of a solid with low molar Si/Al ratio (1.7), with high availability of ion exchange sites and high surface area/small particle size, allowing easy diffusion of metal ions to adsorbent active sites. As a consequence, an excellent performance on removal of Cd2+, Zn2+ and Cu2+ ions was found for this solid. The adsorption capacity followed the order Cd2+ (133 mg·g−1) > Zn2+ (115 mg·g−1) > Cu2+ (99 mg·g−1), which agrees with the order of increasing absolute values of the hydration energy of the metal ions. Kinetic studies and adsorption isotherms showed that the metal ion removal takes place by ion exchange on the monolayer surface of the nano-faujasite. The electrochemical recovery of copper in metallic form exhibited an efficiency of 80.2% after 120 min, which suggests that this process can be adequately implemented for full-scale metal removal.

PREPARATION AND PROPERTIES OF TRANSKETOLASE FROM PORK LIVER

1960 ◽  
Vol 38 (1) ◽  
pp. 115-124 ◽  
Author(s):  
F. J. Simpson
Keyword(s):  
Heavy Metal ◽  
Metal Ions ◽  
Heavy Metal Ions ◽  
Thiamine Pyrophosphate ◽  
Magnesium Ions ◽  
Optimum Activity ◽  
Pork Liver ◽  
High Concentrations ◽  
The Stability ◽  
Ph Range

Transketolase of pork liver has been purified 90-fold and separated from ribulose 5-phosphate 3-epimerase. The transketolase is most stable between pH 7.5 and 8.5 and below 40 °C. The pH range for optimum activity is between 7.6 and 8.1. Activation by magnesium ions or thiamine pyrophosphate could not be demonstrated, but thiamine pyrophosphate increased the stability of the enzyme. Sulphydryl agents, such as p-chloromercuriphenyl sulphonic acid and N-ethylmaleimide, and heavy metal ions, such as cupric, mercuric, and zinc, at relatively high concentrations inhibited the enzyme.

scholarly journals Comparison of Inflammatory Effects in THP-1 Monocytes and Macrophages after Exposure to Metal Ions

Materials ◽  
2020 ◽  
Vol 13 (5) ◽  
pp. 1150
Author(s):  
Henrike Loeffler ◽  
Anika Jonitz-Heincke ◽  
Kirsten Peters ◽  
Brigitte Mueller-Hilke ◽  
Tomas Fiedler ◽  
...  
Keyword(s):  
Metal Ions ◽  
Metal Ion ◽  
Cell Types ◽  
Cell Number ◽  
Corrosion Products ◽  
Proinflammatory Mediators ◽  
Csf Proteins ◽  
Monocytes And Macrophages ◽  
High Concentrations ◽  
Negative Controls

Monocytes and macrophages are the first barrier of the innate immune system, which interact with abrasion and corrosion products, leading to the release of proinflammatory mediators and free reactive molecules. The aim of this study was to understand inflammation-relevant changes in monocytes and macrophages after exposure to corrosion products. To do this, the THP-1 cell line was used to analyze the effects of metal ions simultaneously in monocytes and differentiated macrophages. Cells were stimulated with several concentrations of metal salts (CoCl2, NiCl2, CrCl3 × 6H2O) to analyze viability, gene expression, protein release and ROS production. Untreated cells served as negative controls. While exposure to Cr(3+) did not influence cell viability in both cell types, the highest concentration (500 µM) of Co(2+) and Ni(2+) showed cytotoxic effects mirrored by significantly reduced metabolism, cell number and a concomitant increase of ROS. The release of IL-1β, IL-8, MCP-1 and M-CSF proteins was mainly affected in macrophages after metal ion exposure (100 µM), indicating a higher impact on pro-inflammatory activity. Our results prove that monocytes and macrophages react very sensitively to corrosion products. High concentrations of bivalent ions lead to cell death, while lower concentrations trigger the release of inflammatory mediators, mainly in macrophages.

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