A new Schiff's base ligand immobilized agarose membrane optical sensor for selective monitoring of mercury ion

A highly selective optical sensor was developed for the Hg(2+) determination by chemical immobilization of 2-[(2-sulfanylphenyl)ethanimidoyl]phenol (L), on an agarose membrane. Spectrophotometric studies of complex formation between the Schiff's base ligand L and Hg(2+), Sr(2+), Mn(2+), Cu(2+), Al(3+), Cd(2+), Zn(2+), Co(2+) and Ag(+) metal ions in methanol solution indicated a substantially larger stability constant for the mercury ion complex. Consequently, the Schiff's base L was used as an appropriate ionophore for the preparation of a selective Hg(2+) optical sensor, by its immobilization on a transparent agarose film. A distinct color change, from yellow to green-blue, was observed by contacting the sensing membrane with Hg(2+) ions at pH 4.5. The effects of pH, ionophore concentration, ionic strength and reaction time on the immobilization of L were studied. A linear relationship was observed between the membrane absorbance at 650 nm and Hg(2+) concentrations in a range from 1×10(-2) to 1×10(-5) mol L(-1) with a detection limit (3σ) of 1×10(-6) mol L(-1). No significant interference from 100 times concentrations of a number of potentially interfering ions was detected for the mercury ion determination. The optical sensor was successfully applied to the determination of mercury in amalgam alloy and spiked water samples.     

Methionine-pyrene hybrid based fluorescent probe for trace level detection and estimation of Hg(II) in aqueous environmental samples: experimental and computational studies

A new fluorescent, Hg(2+) selective chemosensor, 4-methylsulfanyl-2-[(pyren-4-ylmethylene)-amino] butyric acid methyl ester (L, MP) was synthesized by blending methionine with pyrene. It was well characterized by different analytical techniques, viz. (1)H NMR, (13)C NMR, QTOF mass spectra, elemental analysis, FTIR and UV-vis spectroscopy. The reaction of this ligand with Hg(2+) was studied by steady state and time-resolved fluorescence spectroscopy. The Hg(2+) complexation process was confirmed by comparing FTIR, UV-vis, thermal, QTOF mass spectra and (1)H NMR data of the product with that of the free ligand values. The composition (Hg(2+):L=1:1) of the Hg(2+) complex in solution was evaluated by fluorescence titration method. Based on the chelation assisted fluorescence quenching, a highly sensitive spectrofluorometric method was developed for the determination of trace amounts of Hg(2+) in water. The ligand had an excitation and emission maxima at 360 nm and 455 nm, respectively. The fluorescence life times of the ligand and its Hg(2+) complex were 1.54 ns and 0.72 ns respectively. The binding constant of the ligand, L with Hg(2+) was calculated using Benesi-Hildebrand equation and was found to be 7.5630×10(4). The linear range of the method was from 0 to 16 μg L(-1) with a detection limit of 0.056 μg L(-1) for Hg(2+). The quantum yields of the ligand and its Hg(2+) complex were found to be 0.1206 and 0.0757 respectively. Both the ligand and its Hg(2+) complex have been studied computationally (Ab-initio, Hartree Fock method) to get their optimized structure and other related physical parameters, including bond lengths, bond angles, dipole moments, orbital interactions etc. The binding sites of the ligand to the Hg(2+) ion as obtained from the theoretical calculations were well supported by (1)H NMR titration. The interference of foreign ions was negligible. This method has been successfully applied to the determination of mercury(II) in industrial waste water.     

In situ measurements of aggregation and disaggregation of Cu(II) complex at liquid/liquid interface

Aggregation of Cu(II)-5-(octadecyloxy)-2-(2-thiazolylazo)phenol (TARC18) complex at the heptane/water interface was measured directly by a centrifugal liquid membrane spectrometry and a two-phase microflow API-MS method. When the pH of an aqueous phase was increased from 4 to 6, the 1:1 complex of Cu(II)-TARC18, which was formed as a positively charged complex at the interface, formed further an aggregate, accompanied by the change of spectra suggesting its aggregation. The MS spectra of the interfacial species indicated the formation of 2:3 complex for Cu(II) and TARC18 under the conditions that the aggregate was formed. This observation allowed us to analyze the interfacial aggregation stoichiometrically: the aggregate of the 2:3 complex was formed from a 1:1 complex at the interface. The addition of purine base of adenine or guanine into the system resulted in the disruption of the aggregate by the formation of a new three-element complex of 1:1:1 for Cu(II), TARC18, and the base, showing a bathochromic shift in the spectra. Thus, the disaggregation experiment showed an interfacial molecular recognition ability of the Cu(II)-TARC18 aggregate for hydrophobic bases.     

Utilization of barley straws as biosorbents for Cu2+ and Pb2+ ions

The potential to remove Cu(2+) and Pb(2+) ion from aqueous solutions through biosorption using barley straw (BS) was investigated in batch experiments. The main parameters influencing Cu(2+) and Pb(2+) ion sorption on BS were: initial metal ion concentration, amount of adsorbent, contact time and pH value of solution. The influences of initial Cu(2+) and Pb(2+) ion concentration (0.1-1mM), pH (2-9), contact time (10-240 min) and adsorbent amount (0.1-1.0 g) have been reported. Equilibrium isotherms have been measured and modelled. The percent adsorption of Cu(2+) and Pb(2+) ions increased with an increase in pH and dosage of treated BS. The biosorptive capacity of the BS was dependent on the pH of Cu(2+) and Pb(2+) ion solution. Adsorption of Cu(2+) and Pb(2+) ion was in all cases pH dependent showing a maximum at equilibrium pH value at 6.0. The equilibrium sorption capacities of Cu(2+) and Pb(2+) after 2h were 4.64 mg/g and 23.20mg/g for BS, respectively. The adsorption data fit well with the Langmuir isotherm model and the experimental result inferred that complexation on surface, adsorption (chemisorption) and ion exchange is one of the major adsorption mechanisms for binding Cu(2+) and Pb(2+) ion to the sorbents.     

Sulfidation treatment of copper-containing plating sludge towards copper resource recovery

The present study is concerned with the sulfidation treatment of copper-containing plating sludge towards copper resource recovery by flotation of copper sulfide from treated sludge. The sulfidation treatment was carried out by contacting simulated or real copper plating sludge with Na(2)S solution for a period of 5 min to 24 h. The initial molar ratio of S(2-) to Cu(2+) (S(2-) to Me(2+) in the case of real sludge) was adjusted to 1.00, 1.25 or 1.50, while the solid to liquid ratio was set at 1:50. As a result, it was found that copper compounds were converted to various copper sulfides within the first 5 min. In the case of simulated copper sludge, CuS was identified as the main sulfidation product at the molar ratio of S(2-) to Cu(2+) of 1.00, while Cu(7)S(4) (Roxbyite) was mainly found at the molar ratios of S(2-) to Cu(2+) of 1.50 and 1.25. Based on the measurements of oxidation-reduction potential, the formation of either CuS or Cu(7)S(4) at different S(2-) to Cu(2+) molar ratios was attributed to the changes in the oxidation-reduction potential. By contrast, in the case of sulfidation treatment of real copper sludge, CuS was predominantly formed, irrespective of S(2-) to Me(2+) molar ratio.     

The use of Bacillus subtilis immobilized on Amberlite XAD-4 as a new biosorbent in trace metal determination

The present work proposes the use of Bacillus subtilis immobilized on Amberlite XAD-4 as new biosorbent in trace metal determination. The procedure is based on the biosorption of Cu and Cd ions on a column of Amberlite XAD-4 resin loaded with dried, dead bacterial components prior to their determination by flame AAS. Various parameters such as pH, amount of adsorbent, eluent type and volume, flow rate of solution and matrix interference effect on the retention of the metal ions have been studied. The optimum pH values of quantitative sorption for Cu and Cd were found to be 7.0 and 7.5, respectively. These metal ions can be desorbed with 1M HCl (recovery, 96-100%). The sorption capacity of the resin was 0.0297 and 0.035 mmol g(-1) for Cu(2+) and Cd(2+), respectively. The tolerance limit of some electrolytes were also studied. This procedure was applied to Cu(2+) and Cd(2+) determination in aqueous solutions, including river and well water systems. In order to evaluate the accuracy of the proposed procedure, the certified reference materials, NRCC-SLRS-4 Riverine water and LGC7162 Strawberry leaves were analyzed.     

Enhanced luminescence of lanthanide complexes by silver nanoparticles for ciprofloxacin determination

We present the enhancement of luminescence of europium complex, Eu(3+)-ciprofloxacin (CIP), in the presence of silver nanoparticles (Ag NPs) for the CIP determination. The increment of the luminescence intensity of the Eu(3+)-CIP complex with Ag NPs was obtained due to the transfer of resonance energy to the fluorophores through the interaction of the excited-state fluorophores and surface plasmon electron in the metal nano surface. The luminescence intensity of Eu3+ was enhanced by complexation with CIP at 614 nm after excitation at 373 nm corresponding to the 5D0-7F2 transitions of Eu3+ ion. Based on the above phenomenon, a sensitive and rapid spectrofluorimetric method has been developed for the CIP determination. Linearity of the calibration curve was obtained in the range of 2.0 x 10(-10)-1.0 x 10(-8) g mL(-1) with correlation coefficient of 0.9992. The limit of detection of CIP was found to be 1.9 x 10(-11) g mL(-1) with the relative standard deviation (RSD) of 1.19% for 5 replicate measurements of 5.0 x 10(-7) g mL(-1) of CIP. The present method has been successfully applied for CIP determination in pharmaceutical and biological samples.     

Simultaneous preconcentration and determination of copper, nickel, cobalt and lead ions content by flame atomic absorption spectrometry

A sensitive and simple method for the simultaneous preconcentration of nutritionally important minerals in real samples has been reported. The method is based on the formation of metal complexes by 4,6-dihydroxy-2-mercaptopyrimidine (DHMP) loaded on activated carbon. The metals content on the complexes are then eluted using 5 mL 2M HNO(3) in acetone, which are detected by AAS at resonance line. In this procedure, minerals such as Cu, Ni, Pb and Co could be analyzed in one run by caring out the simultaneous separation and quantification of them. At optimum condition the response are linear over concentration range of 0.04-1.1 microg mL(-1) for Ni(2+) and 0.04-1.0 microg mL(-1) for Cu(2+), Pb(2+) and Co(2+). The detection limits of each element are expressed as the amount of analytes in ng mL(-1) giving a signal to noise ratio of 3 are equal to 3.5, 3.4, 2.9 and 8.4 for Ni(2+), Co(2+), Cu(2+) and Pb(2+). The sorption capacity was determined by saturating 0.5 g solid phase. The loading capacity are 0.54, 0.53, 0.63 and 0.45 mg g(-1) for Ni(2+), Co(2+), Cu(2+) and Pb(2+). The ability of method for repeatable recovery of trace ion are 99.0, 98.9, 99.2 and 98.8 with R.S.D. of 1.4, 1.3, 1.2 and 1.4 for Ni(2+), Co(2+), Cu(2+) and Pb(2+). The low detection limits of these elements in this technique make it a superior alternative to UV-vis and in several applications, also an alternative to ICP-MS techniques. The method has been successfully applied for these metals content evaluation in some real samples including natural water, leaves of spinach and cow liver.     

Fluorescence quenching of the europium tetracycline hydrogen peroxide complex by copper (II) and other metal ions

The europium-tetracycline complex [Eu(Tc)] is known to show only weak fluorescence with an emission maximum at 615 nm. On addition of hydrogen peroxide (HP), the strongly fluorescent [Eu(Tc)(HP)] complex is formed, which displays a 15-fold stronger luminescence intensity. This study describes the decrease in luminescence intensity of the [Eu(Tc)(HP)] complex in aqueous solution in the presence of Cu2+, Fe3+, Ag+, Al3+, Zn2+, Co2+, Ni2+, Mn2+, Ca2+, and Mg2+. Static and dynamic quenching can be induced by Cu2+, and these processes were quantified by means of their quenching constants. Stern-Volmer plots were also derived from lifetime imaging measurements accomplished by the rapid lifetime determination (RLD) technique based on microwell plate assays, and also by the time-correlated single photon counting (TCSPC) technique. According to those data, a time-resolved fluorescent method for copper determination can be proposed that is based on dynamic quenching of the [Eu(Tc)(HP)] complex by Cu2+ ions. The response to copper concentrations is linear up to 1.6 micromol L(-1), providing a detection limit of 0.2 micromol L(-1).     

A solid phase extraction procedure for Fe3+, Cu2+ and Zn2+ ions on 2-phenyl-1H-benzo[d] imidazole loaded on Triton X-100-coated polyvinyl chloride

A new and efficient solid phase extraction method is described for the preconcentration of trace heavy metal ions. The method is based on the adsorption of Fe(3+), Cu(2+) and Zn(2+) on 2-phenyl-1H-benzo[d] imidazole (PHBI) loaded on Triton X-100-coated polyvinyl chloride (PVC). The influences of the analytical parameters including pH and sample volume were investigated. Common coexisting ions did not interfere on the separation and determination of analytes under study. The adsorbed analytes were desorbed by using 5 mL of 4 mol L(-1) nitric acid. The preconcentration factor is 90. The detection limits (3 sigma) were in the range of 0.95-1 microg L(-1). The sorbent exhibited excellent stability and its sorption capacity under optimum conditions has been found to be more than 2.7 mg of ions per gram of sorbent. The recoveries of analytes were generally higher than 95%. The relative standard deviations (R.S.D.s) were generally lower than 4%. The method has been successfully applied to some real samples.     

Dual-emission fluorescent silica nanoparticle-based probe for ultrasensitive detection of Cu2+

An effective dual-emission fluorescent silica nanoparticle-based probe has been constructed for rapid and ultrasensitive detection of Cu(2+). In this nanoprobe, a dye-doped silica core served as a reference signal, thus providing a built-in correction for environmental effects. A response dye was covalently grafted on the surface of the silica nanoparticles through a chelating reagent for Cu(2+). The fluorescence of the response dye could be selectively quenched in the presence of Cu(2+), accompanied by a visual orange-to-green color switch of the nanoprobe. The nanoprobe provided an effective platform for reliable detection of Cu(2+) with a detection limit as low as 10 nM, which is nearly 2 × 10(3) times lower than the maximum level (～20 μM) of Cu(2+) in drinking water permitted by the U.S. Environmental Protection Agency (EPA). The high sensitivity was attributed to the strong chelation of Cu(2+) with polyethyleneimine (PEI) and a signal amplification effect. The nanoprobe constructed by this method was very stable, enabling the rapid detection of Cu(2+) in real water samples. Good linear correlations were obtained over the concentration range from 1 × 10(-7) to 8 × 10(-7) (R(2) = 0.99) with recoveries of 103.8-99.14% and 95.5-95.14% for industrial wastewater and lake water, respectively. Additionally, the long-wavelength emission of the response dye can avoid the interference of the autofluorescence of the biosystems, which facilitated their applications in monitoring Cu(2+) in cells. Furthermore, the nanoprobe showed a good reversibility; the fluorescence can be switched "off" and "on" by an addition of Cu(2+) and EDTA, respectively.     

Copper-iron bimetal modified PAN fiber complexes as novel heterogeneous Fenton catalysts for degradation of organic dye under visible light irradiation

A series of Cu-Fe bimetal amidoximated polyacrylonitrile (PAN) fiber complexes with different molar ratios of Cu(2+) to Fe(3+) ions was prepared using a simple exhaustion method, and characterized using FTIR, DRS and XPS, respectively. Then they were tested as the heterogeneous Fenton catalysts for Rhodamine B degradation with H(2)O(2) in the dark and under visible light irradiation. The results indicated that Cu-Fe bimetal amidoximated PAN fiber complexes could more effectively catalyze the dye degradation in water than Fe amidoximated PAN fiber complex, especially in the dark. And introduction of Cu(2+) ions significantly increased their catalytic performance. 0.56 was the optimum molar ratio of Cu(2+) to Fe(3+) ions to achieve the best catalytic activity and stability. This was mainly due to the synergetic effect in the bimetal complexes. Visible light irradiation improved the catalytic activity of the complexes, especially with a low molar ratio of Cu(2+) to Fe(3+) ions.     

A turn-on fluorescent sensor for pyrophosphate based on the disassembly of Cu2+-mediated perylene diimide aggregates

A complex between an anionic perylene diimide derivative (PDI-GlyAsp) and cupric ion has been prepared and applied to be turn-on fluorescent probe for the detection of pyrophosphate (PPi) in 100% aqueous solution. The complex formation process and PPi detection have been studied by absorption and emission spectroscopy. It was confirmed that the introduction of cupric ion into PDI-GlyAsp solution resulted in the assembly of PDI-GlyAsp into PDI-GlyAsp/Cu(2+) aggregates, leading to the fluorescence quenching of PDI-GlyAsp. Upon addition of PPi into the above solution led to the disassembly of the aggregates due to the competitive binding of PPi with Cu(2+) in the PDI-GlyAsp/Cu(2+) complex, and a recovery of PDI-GlyAsp emission was observed. Therefore, the PDI-GlyAsp/Cu(2+) complex can be applied as a turn-on fluorescent probe for detecting PPi with high selectivity and sensitivity.     

Colorimetric detection of trace copper ions based on catalytic leaching of silver-coated gold nanoparticles

A colorimetric, label-free, and nonaggregation-based silver coated gold nanoparticles (Ag/Au NPs) probe has been developed for detection of trace Cu(2+) in aqueous solution, based on the fact that Cu(2+) can accelerate the leaching rate of Ag/Au NPs by thiosulfate (S(2)O(3)(2-)). The leaching of Ag/Au NPs would lead to dramatic decrease in the surface plasmon resonance (SPR) absorption as the size of Ag/Au NPs decreased. This colorimetric strategy based on size-dependence of nanoparticles during their leaching process provided a highly sensitive (1.0 nM) and selective detection toward Cu(2+), with a wide linear detection range (5-800 nM) over nearly 3 orders of magnitude. The cost-effective probe allows rapid and sensitive detection of trace Cu(2+) ions in water samples, indicating its potential applicability for the determination of copper in real samples.     

Metal ion (silver, cadmium and zinc ions) modified CdS quantum dots for ultrasensitive copper ion sensing

Metal ion (Ag(+), Cd(2+), Zn(2+)) modified CdS quantum dots (QDs) were synthesized and used for Cu(2+) sensing. Modification by these metal ions could enhance the PL intensity of CdS QDs with the extent of the PL enhancement being related to the concentration of the metal ions. Different metal ion (Ag(+), Cd(2+), Zn(2+)) modified CdS QDs also showed different analytical characteristics for Cu(2+) sensing. In particular, Ag( + ) modified CdS QDs showed greatly enhanced sensitivity for Cu(2+) determination than did the unmodified CdS QDs. A limit of detection (LOD) of 2.0 × 10(-10) M was obtained for Ag(+) modified CdS QDs, which is the lowest LOD obtained using QDs as fluorescence probes for Cu(2+) sensing. This study demonstrates the important role of surface state of QDs in fluorescence sensing.     

Effect of acclimatization of microorganisms to heavy metals on the performance of activated sludge process

Although selected heavy metals (HMs) stimulate biological reactions at low concentrations, all HMs are toxic to microorganisms (MOs) at moderate concentrations and can cause inhibitory effects on the biological processes. Therefore, MOs must be acclimated to HMs or other toxic substances present in wastewaters (WWs) before they are used in an activated sludge process (ASP). In this study, combined effect of Cu(2+) and Zn(2+) ions in a synthetic WW on the efficiency of a laboratory-scale ASP without recycle was investigated using acclimated MOs at different extents.A synthetic feed solution of 1222 mg L(-1) proteose-peptone (corresponding to 1300 mg COD L(-1)) served as a source of carbon. Cu(2+) and Zn(2+) ions at different concentrations (1.5, 4.5 and 9, 27 mg L(-1), respectively) were introduced in the feed to a continuously stirred activated sludge reactor at different hydraulic residence times (2-40 h) keeping pH, temperature and stock feed composition constant. The combined effects of copper and zinc ions were determined by mixing these metallic ions at the specified combinations of concentrations such as "1.5 mg L(-1) of Cu(2+)+9 mg L(-1) of Zn(2+)" and "4.5 mg L(-1) of Cu(2+)+27 mg L(-1) of Zn(2+)". It was observed that using seed MOs acclimatized to two times of the combined threshold concentration of these HMs for an unduly long period of time (1-4 months) caused adverse effects on the ASP performance. Besides, it was found that usual inhibition effects of these HMs were enhanced with increasing period of acclimation. Substantially lower substrate removal efficiencies were obtained with acclimatized MOs than those obtained with non-acclimatized MOs. At the higher initial substrate concentration of 2500 mg COD L(-1), substrate-inhibition occurred causing a decrease in the specific growth rate constant (k); however, HM inhibition was suppressed, resulting to about 20% increase in treatment efficiency of the ASP. It can be concluded that the time period necessary for acclimatization of seed MOs must be adjusted carefully with concentrations of HMs lower than their threshold concentrations to achieve an optimal operation of an aerobic biological process.     

Preconcentration and separation of trace amount of heavy metal ions on bis(2-hydroxy acetophenone)ethylendiimine loaded on activated carbon

A sensitive and simple method for simultaneous preconcentration of trace heavy metal ions in some food samples has been reported. The method is based on the adsorption of Cr(3+), Fe(3+), Cu(2+), Ni(2+), Co(2+) and Zn(2+) on bis(2-hydroxy acetophenone)ethylendiimine (BHAPED) loaded on activated carbon (AC). The adsorbed metals on activated carbon were eluted using 2 mol L(-1) nitric acid in acetone. The influences of the analytical parameters including pH and sample volume were investigated. The effects of matrix ions on the recoveries of analyte ions were also investigated. The recoveries of analytes were generally higher than 94%. The method has been successfully applied for analysis of the metal contents in real samples including natural water samples.     

Metalation states versus enzyme activities of Cu, Zn-superoxide dismutase probed by electrospray ionization mass spectrometry

Cu, Zn-superoxide dismutase (SOD-1), an enzyme that catalyzes the disproportionation reaction of superoxide to produce oxygen and hydrogen peroxide, thereby protecting cells from oxidative stress, is a homodimer that coordinates one copper and one zinc ion per monomer. Cu (2+) and Zn (2+) ions play important roles in enzyme activity and structural stability, respectively. In addition, dimer formation is also essential for fulfilling the function of SOD-1. We here report on the reconstitution and enzyme activities of several metalation states of SOD-1 (Cu 4-, Cu 3Zn-, and Cu 2Zn 2-homodimers). Each metalation state of the reconstituted SOD-1 could be unambiguously differentiated by electrospray ionization mass spectrometry, the metal ions of which had been completely replaced by 99 atom % (63)Cu and (68)Zn stable isotopes. It was found that (1) the Cu 4-dimer possessed 84% of the activity of the native enzyme, (2) the Cu-site resisted being coordinated with Zn (2+) ions while the Zn-site could be bound with Cu (2+) ions, and (3) the simultaneous addition of the Cu (2+) and Zn (2+) ions to generate a fully metalated form produced the multiply metalated SOD-1 (Cu 4-, Cu 3Zn-, and Cu 2Zn 2-dimers), which were clearly distinguishable from one another by the use of the stable isotopes, while the sequential addition of Zn (2+) followed by the Cu (2+) ion predominantly produced a Cu 2Zn 2-dimer comparable to the native enzyme.     

Mercury/homocysteine ligation-induced ON/OFF-switching of a T-T mismatch-based oligonucleotide molecular beacon

A molecular beacon (MB) with stem-loop (hairpin) DNA structure and with attached fluorophore-quencher pair at the ends of the strand has been applied to study the interactions of Hg(2+) ions with a thymine-thymine (T-T) mismatch in Watson-Crick base-pairs and the ligative disassembly of MB·Hg(2+) complex by Hg(2+) sequestration with small biomolecule ligands. In this work, a five base-pair stem with configuration 5'-GGTGG...CCTCC-3' for self-hybridization of MB has been utilized. In this configuration, the four GC base-pair binding energy is not sufficient to hybridize fully at intermediate temperatures and to form a hairpin MB conformation. The T-T mismatch built-in into the stem area can effectively bind Hg(2+) ions creating a bridge, T-Hg-T. We have found that the T-Hg-T bridge strongly enhances the ability of MB to hybridize, as evidenced by an unusually large MB melting temperature shift observed on bridge formation, ΔT(m) = +15.1 ± 0.5 °C, for 100 nM MB in MOPS buffer. The observed ΔT(m) is the largest of the ΔT(m) found for other MBs and dsDNA structures. By fitting the parameters of the proposed model of reversible MB interactions to the experimental data, we have determined the T-Hg-T bridge formation constant at 25 °C, K(1) = 8.92 ± 0.42 × 10(17) M(-1) from mercury(II) titration data and K(1) = 1.04 ± 0.51 × 10(18) M(-1) from the bridge disassembly data; ΔG° = -24.53 ± 0.13 kcal/mol. We have found that the biomarker of oxidative stress and cardiovascular disease, homocysteine (Hcys), can sequester Hg(2+) ions from the T-Hg-T complex and withdraw Hg(2+) ions from MB in the form of stable Hg(Hcys)(2)H(2) complexes. Both the model fitting and independent (1)H NMR results on the thymidine-Hg-Hcys system indicate also the high importance of 1:1 complexes. The high value of K(1) for T-Hg-T bridge formation enables analytical determinations of low concentrations of Hg(2+) (limit of detection LOD = 19 nM or 3.8 ppb, based on 3σ method) and Hcys (LOD = 23 nM, 3σ method). The conditional stability constants for Hg(Hcys)H(2)(2+) and Hg(Hcys)(2)H(2) at 52 °C have been determined, β(112) = 5.37 ± 0.3 × 10(46) M(-3), β(122) = 3.80 ± 0.6 × 10(68) M(-4), respectively.     

Preconcentration of Pb(II), Cr(III), Cu(II), Ni(II) and Cd(II) ions in environmental samples by membrane filtration prior to their flame atomic absorption spectrometric determinations

A method for separation-preconcentration of Pb(II), Cr(III), Cu(II), Ni(II) and Cd(II) ions by membrane filtration has been described. The method based on the collection of analyte metal ions on a cellulose nitrate membrane filter and determination of analytes by flame atomic absorption spectrometry (FAAS). The method was optimized for several parameters including of pH, matrix effects and sample volume. The recoveries of analytes were generally in the range of 93-100%. The detection limits by 3 sigma for analyte ions were 0.02microgL(-1) for Pb(II), 0.3microgL(-1) for Cr(III), 3.1microgL(-1) for Cu(II), 7.8microgL(-1) for Ni(II) and 0.9microgL(-1) for Cd(II). The proposed method was applied to the determination of lead, chromium, copper, nickel and cadmium in tap waters and RM 8704 Buffalo River Sediment standard reference material with satisfactory results. The relative standard deviations of the determinations were below 10%.