Preconcentration of some metals using metalfix chelamine resin prior to ICP-AES analysis

Preconcentration and separation of Ni, Pb and Cd have been investigated using the metalfix chelamine resin prior to inductively coupled plasma – atomic emission spectrometry (ICP-AES) under various experimental conditions. The recoveries of the analytes obtained with 95% confidence level were 92 ± 1% for Ni, 100 ± 4% for Pb and 93 ± 3% for Cd. Received: 5 February 1998 / Revised: 30 April 1998 / Accepted: 12 June 1998     

Trace elements in Variegated Bolete (Suillus variegatus) fungi

Metallic elements such as Ag, Al, Ba, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, Pb, Rb, Sr, and Zn were determined using ICP-OES in a representative set of fifteen fruiting bodies of the edible fungus Suillus variegatus. Fruiting bodies were collected from unpolluted areas near the village of Lubichowo of the Bory Tucholskie forest complex in northern Poland in 2007?C2008. The caps were richer in Ag, Al, Cd, Cr, Cu, Fe, K,Mg, Ni, Rb, and Zn, and the stipes in Ba, Ca, Mn, Na, Pb, and Sr. Cobalt concentration in the caps and stipes was similar. In the caps, the content of the elements decreased in the order (mg per kg of dry weight): K 29000 ± 3700, Fe 1600 ± 80, Mg 990 ± 110, Rb 320 ± 86, Zn 90 ± 19, Ca 75 ± 34, Al 68 ± 32, Na 40 ± 18, Cu 19 ± 7, Mn 13 ± 7, Cd 1.0 ± 0.5, Ni 0.64 ± 0.32, Ag 0.40 ± 0.20, Cr 0.33 ± 0.06, Pb 0.20 ± 0.17, Ba 0.19 ± 0.11, Sr 0.15 ± 0.09, and Co 0.070 ± 0.050. Apparently, S. variegatus collected from background areas are relatively low in Pb and Cd and so are suitable for human consumption.     

Assessment of Heavy Metal Pollution and Ecological Risk of Roadside Soils in Tlemcen (Algeria) Using Flame-Atomic Absorption Spectrometry

In Algeria, few studies have been conducted on the evaluation of roadside soil pollution. A total of 34 soil samples (28 roadside and 6 off-road) was obtained at 0–20?cm depth along the RN 35 national road. Heavy metal (Cd, Cr, Cu, Fe, Ni, Pb, and Zn) contents were extracted using aqua regia digestion and determined using atomic absorption spectrometry. Background values of heavy metal contents were determined using the robust statistical method of median plus two times the median absolute deviation. Single- and multi-element pollution and ecological risk indices were calculated. The results showed that background values were 2.5?±?0.3, 64.9?±?8.1, 28.0?±?4.1, 29371.5?±?4403.0, 32.9?±?4.4, 72.2?±?12.8, and 445.1?±?62.9?mg/kg for Cd, Cr, Cu, Fe, Ni, Pb, and Zn, respectively. The results were all higher than their corresponding median values. Single-element pollution indices (enrichment factor and geoaccumulation index) showed that the pollution is primarily due to Pb and Zn. Multi-element pollution index (Nemerow index) indicated that only 3% of the soil samples are strongly contaminated, whereas 23% are seriously contaminated. The potential ecological risk index showed that Cd is the most harmful element, followed by Pb and Zn. 65% of the soil samples had moderate potential ecological risk, while only 3% had considerable potential ecological risk. This study may be used as a baseline for future monitoring and as a tool for decision-making regarding environmental protection policies and sustainability of this semiarid agroecosystem.     

Pulverized Banana Peel as an Economical Sorbent for the Preconcentration of Metals

A procedure for the determination of trace levels of Cd, Co, Cr, Fe, Mn, Ni, and Pb by flame atomic absorption spectrometry using a column preconcentration system is described in which the metals were adsorbed on pulverized banana peel, an economically and environmentally acceptable sorbent. In the optimization procedure, five variables (sample pH, mass of biosorbent, type of eluent, sample flow rate, and volume) were optimized and the capacity of the biosorbent was established. Under the optimized conditions, the detection limits of the method were 2.4, 27.0, 49.4, 31.1, 6.7, 29.6, and 46.2 µg L^?1 for Cd, Co, Cr, Fe, Mn, Ni, and Pb, respectively. The precision, expressed as relative standard deviation, was less than 4% based on twelve measurements. The recoveries were 81.1% (Cd), 91.4% (Co), 87.2% (Cr), 90.1% (Fe), 88.0% (Mn), 94.1% (Ni), and 93.2% (Pb) under the optimum conditions (pH; 9, sample flow rate; 3 mL min^?1, mass of biosorbent; 200 mg; eluent; 1 mol L^?1 nitric acid, preconcentration factor; 10). The sorption capacity of pulverized banana peel was 15.12, 28.85, 32.70, 30.44, 30.94, 28.97, and 8.21 µmol per gram of adsorbent for Cd, Co, Cr, Fe, Mn, Ni, and Pb, respectively.     

Interactive effects of age and gender on levels of toxic and potentially toxic metals in children hair in different urban environments

Children growth and development may be affected by metal exposure. The objective of the present study was to investigate the interactive effects of age and gender on children hair toxic metal levels in urban environment of two Russian cities. A total of 2021 children living in Moscow and Novosibirsk aged 1–18 years old were examined. Hair Al, As, Cd, Hg, Ni, Pb and Sn levels were assessed using inductively-coupled plasma mass-spectrometry in dynamic reaction cell mode. Children from Novosibirsk were characterised by higher hair Al (37%), As (385%), Cd (127%), Hg (11%), Ni (23%), Pb (72%) and Sn (25%) in comparison to Moscow values. In the general cohort, boys had higher Al (13%), As (51%), Cd (65%), Pb (63%) and Sn (18%) levels, whereas hair Ni was higher in girls (17%). Further analysis demonstrated age-specific gender differences. In particular, only hair Ni and Cd levels were higher in male toddlers and pre-schoolers from Novosibirsk as compared to females. No gender difference was detected in Moscow. Maximal gender differences in hair metal levels were detected in adolescents for both locations. International Union of Pure and Applied Chemistry (IUPAC) reference values for all groups were also calculated. The overall reference limits for the studied children population were Al (1.335–3.340 µg/g), As (0.021–0.384 µg/g), Cd (0.000–1.389 µg/g), Hg (0.024–0.722 µg/g), Ni (0.076–0.701 µg/g), Pb (0.050–1.490 µg/g) and Sn (0.070–1.026 µg/g). Two-way ANOVA demonstrated significant effects of age, gender and age*gender interaction on hair metals in both cities. At the same time, the age-specific changes in hair metal content were more expressed in children from Novosibirsk, being exposed to higher metal pollution. The obtained data demonstrate that age, gender as well as the particular rate of pollution in each location should be taken into account during interpretation of hair test results.     

Solid phase extraction and diffusive gradients in thin films techniques for determination of total and labile concentrations of Cd(II), Cu(II), Ni(II) and Pb(II) in Black Sea water

Total dissolved and labile concentrations of Cd(II), Cu(II), Ni(II) and Pb(II) were determined at six locations of the Bourgas Gulf of the Bulgarian Black Sea coast. Solid phase extraction procedure based on monodisperse, submicrometer silica spheres modified with 3-aminopropyltrimethoxysilane followed by the electrothermal atomic absorption spectrometry (ETAAS) was developed and applied to quantify the total dissolved metal concentrations in sea water. Quantitative sorption of Cd, Cu, Ni and Pb was achieved in the pH range 7.5–8, for 30?min, adsorbed elements were easily eluted with 2?mL 2?mol?L^?1 HNO₃. Since the optimal pH for quantitative sorption coincides with typical pH of Black Sea water (7.9–8.2), on-site pre-concentration of the analytes without any additional treatment was possible. Detection limits achieved for total dissolved metal quantification were: Cd 0.002?µg?L^?1, Cu 0.005?µg?L^?1, Ni 0.03?µg?L^?1, Pb 0.02?µg?L^?1 and relative standard deviations varied from 5–13% for all studied elements (for typical Cd, Cu, Ni and Pb concentrations in Black Sea water). Open pore diffusive gradients in thin films (DGT) technique was employed for in-situ sampling and pre-concentration of the sea water and in combination with ETAAS was used to determine the proportion of dynamic (mobile and kinetically labile) species of Cd(II), Cu(II), Ni(II) and Pb(II) in the sea water. Obtained results showed strong complexation for Cu and Pb with sea water dissolved organic matter. The ratios between DGT-labile and total dissolved concentrations found for Cu(II) and Pb(II) were in the range 0.2–0.4. For Cd and Ni, these ratios varied from 0.6 to 0.8, suggesting higher degree of free and kinetically labile species of these metals in sea water.     

Simultaneous determination of Cd,Cr, Cu,Ni, Pb and Zn in sewage sludge by slurry introduction ICP-OES method

In order to evaluate the slurry nebulisation method as an alternative method for analysis of sewage sludge, the metal content of sludge samples of different origins was determined. The concentrations of six elements: Cd, Cr, Cu, Ni, Pb, and Zn were determined by introducing the sludge as a slurry into an inductively coupled plasma optical emission spectrometer (ICP-OES). Calibration was performed by using aqueous standard solutions. For comparison, the sewage sludge was also digested by microwave digestion and introduced into the plasma as an aqueous solution. The accuracy of the method was checked by analysing a sewage sludge certified reference material (CRM 007-040 Sewage Sludge). The Student's t-test showed that values obtained using slurry nebulisation were close to the certified values at a 95% confidence level. The values of elements Cd 11.1?±?0.8; Cr 37.7?±?3.3; Cu 563.3?±?38.4; Pb 119.2?±?10.1; Zn 729?±?68.2?mg?kg^?1 obtained using this method were comparable with those obtained using the conventional method. The slurry method can, therefore, be successfully applied to the determination of content of each element in sewage sludge with RSD less than 3%, without the need to predissolve them. This could avoid the use of hazardous chemicals, incomplete dissolution and loss of volatile analytes.     

Solid phase extraction of heavy metal ions based on a novel functionalized magnetic multi-walled carbon nanotube composite with the aid of experimental design methodology

We report that magnetic multiwalled carbon nanotubes functionalized with 8-aminoquinoline can be applied to the preconcentration of Cd(II), Pb(II) and Ni(II) ions. The parameters affecting preconcentration were optimized by a Box-Behnken design through response surface methodology. Three variables (extraction time, magnetic sorbent amount, and pH value) were selected as the main factors affecting sorption, and four variables (type, volume and concentration of the eluent; elution time) were selected for optimizing elution. Following sorption and elution, the ions were quantified by FAAS. The LODs are 0.09, 0.72, and 1.0 ng mL^?1 for Cd(II), Ni(II), and Pb(II) ions, respectively. The relative standard deviations are <5.1 % for five separate batch determinations at 30 ng mL^?1 level of Cd(II), Ni(II), and Pb(II) ions. The sorption capacities (in mg g^?1) of this new sorbent are 201 for Cd(II), 150 for Pb(II), and 172 Ni(II). The composite was successfully applied to the rapid extraction of trace quantities of heavy metal ions in fish, sediment, soil, and water samples.

Determination of Cd and Pb in seawater by graphite furnace atomic absorption spectrometry with the use of hydrofluoric acid as a chemical modifier

High concentration of added hydrogen fluoride converted the seawater chloride to the corresponding fluoride matrix, and the liberated hydrochloric acid could be removed during the drying step. The atomization of cadmium and lead could be performed at a relatively low temperature (∼1300 °C) at which the vaporization of the fluoride matrix was relatively slow, and the corresponding weak background signals could be separated from the analytical signals in time. Experimental conditions for the determination of Cd and Pb in seawater in the presence of HF were optimized with the use of the a priori calculation of the limit of detection. The experimental limit of detection obtained for Cd and Pb were, respectively, 0.007 and 0.25 μg l⁻¹ for a 15-μl seawater sample (3σ, 20 replicates). The concentrations of Cd determined in a SLEW-1 estuarine water and a CASS-2 seawater were 0.020±0.002 and 0.016±0.002 μg l⁻¹ Cd, respectively, in good agreement with the 0.018±0.003 and 0.019±0.004 μg l⁻¹ Cd certified values (At the 95% confident level, 10 replicates).     

Quantification of heavy metals and health risk assessment in processed fruits’ products

Present study was intendant to assess heavy metals (HMs) concentration and associated health risk in processed fruits’ products sold in the local markets of North Pakistan. In total seven metals viz. cadmium (Cd), chromium (Cr), cobalt (Co), copper (Cu), iron (Fe), lead (Pb) and zinc (Zn) were quantified in 345 samples of different brands categorized into eight groups (Sauces, Ketchup, Juices, Jams, canned fruits, tomato paste, marmalades and pickles). On the comparative basis, Fe was dominating with highest concentration in pickles, canned fruits and sauces at 143.3 ± 43.2, 83.64 ± 23.19 and 50.17 ± 15.1 mg/kg, respectively), followed by Cd in sauces (22.94 ± 6.91 mg/kg), Cr in juices (12.97 ± 3.91 mg/kg) and Pb in pickles (12.53 ± 3.77 mg/kg). Measured levels of these metals varied significantly and were relatively higher than their permissible limits. Univariate and multivariate analysis depicted strong association among Cr, Co, Pb and Fe and confirmed HMs contamination through natural and anthropogenic sources in processed foods. Health risk index (HRI) for Cd, Cr and Pb was greater than unity (<1.0), particularly in sauces, jams and canned fruits. Target hazard quotient (THQ) and hazard index (HI) of Cd, Cr and Pb were relatively high. But target cancer risk (TCR) assessment indicates that these metals were within the acceptable limit, except for Cd concentration in sauces, jams and canned fruits that may cause cancer to consumers.     

黔产市售绿茶重金属的含量特征及健康风险评估

为研究黔产市售绿茶中重金属的含量分布特征及健康风险,以五个生产加工地的黔产市售绿茶为研究对象,分析其9种重金属(Pb、Cr、Cd、Hg、Cu、Zn、Mn、Ni和As)含量,利用美国环境保护署(USEPA)推荐的健康风险评价模型进行人体重金属的健康风险评价。结果表明,五种茶叶中Cr、Cd、Pb、Hg、Cu和As含量均低于国家限量标准。黔产市售绿茶的重金属浸出率大小次序为Zn>Mn>Hg>As>Cd>Pb>Cr>Cu>Ni。健康风险评价结果表明,五个产地的绿茶中重金属通过饮茶途径所产生的健康危害个人年风险大小次序为Cd>As>Mn>Ni>Cr>Hg>Pb>Zn>Cu,茶叶中重金属通过饮茶途径所产生的个人健康危害年风险总和为4.33×10-6~5.73×10-6 a-1,均低于USEPA和ICRP推荐的最大可接受风险水平,表明重金属引起的健康危害极小,其对暴露人群造成的健康危害可忽略不计,绿茶中重金属均处于安全范围内。     

Toxic and essential element concentrations in different honey types

The physicochemical parameters (free acidity, moisture content, sucrose content, hydroxymethylfurfural, reducing sugars, electrical conductivity, diastase activity and water-insoluble content), elements (Cu, Fe, Zn, Mn, Cr, Co, Ni, Se, K, Na, Ca, Mg) and heavy metal/metalloid concentrations (Cd, Hg, Pb and As) of 84 honeys (linden, multifloral, honeydew and acacia) from Serbia, were analyzed using ICP-MS. Concerning the physicochemical parameters, all tested honeys were found to meet European Legislation (EC Directive 2001/110). Potassium was the major element, ranging between 943.9 ± 538.6 mg/kg and 2563 ± 1817 mg/kg. Statistical analysis showed significant differences in the concentrations of Zn, Mn, Co and Na between the honeys. Selenium and Hg levels were below the limits of detection. Positive correlations were found between electrical conductivity and most of the elements. The present study showed that Serbian honey examined were of good quality according to its physicochemical parameters and met safety criteria concerning the concentrations of Cd, Hg, Pb and As.     

Determination of heavy metal traces in metallic materials with IDMS

Summary Two pure copper samples were analysed for Cr, Ni, Zn, Cd, and Pb with isotope dilution mass spectrometry (IDMS) as a part of a certification campaign of the European Community Bureau of Reference in Brussels. Additionally, one commercially available copper powder was determined for Zn, Cd, and Pb. After dissolution of the sample in aqua regia Pb was separated from the matrix by anodic electrodeposition, the other elements by anion-exchange chromatography. Positive thermal ions were produced in a single-filament ion source using the silica gel technique with phosphoric acid for Zn, Cd, and Pb and with boric acid for Cr and Ni. Most of the heavy metals could be determined with relative standard deviations of about 1% down to the ng/g level. The detection limits were 13 ng/g for Zn, 4 ng/g for Ni, 2 ng/g for Cr, 1 ng/g for Pb, and 0.03 ng/g for Cd. The results were compared with those obtained by another IDMS laboratory and by other methods applied during the certification campaign.

---

Bestimmung von Schwermetallspuren in metallischen Werkstoffen mit der massenspektrometrischen IsotopenverdünnungsanalyseTeil 1. Bestimmung von Cr, Ni, Zn, Cd und Pb in reinem Kupfer

     

INAA of essential micronutrients in <Emphasis Type="Italic">Terminalia arjuna</Emphasis> bark powder: a versatile heart tonic

Five bark powder samples of Arjuna (Terminalia arjuna) having different origins including two commercial brands were analyzed for 8 minor (Al, Na, K, Mg, Ca, P, Cl, Fe) and 19 trace (As, Ba, Br, Co, Cr, Cs, Cu, Eu, Hg, La, Mn, Rb, Sb, Sc, Sm, Sr, Th, V, Zn) elements by INAA. Also concentrations of Ni, Cd and Pb were determined by AAS and of Sn by ICP-MS. Arjuna bark powder is enriched in Ca (34.1 ± 10.6 mg/g), Mg (5.41 ± 1.93 mg/g), K (5.87 ± 2.18 mg/g), Cl (4.0 ± 2.2 mg/g) and Fe (2.99 ± 1.77 mg/g) with significant amounts of Cr (6.9 ± 4.0 μg/g), Mn (75.5 ± 24.8 μg/g), Sr (114 ± 69 μg/g) and Zn (11.9 ± 8.9 μg/g). Several toxic elements such as As (78.6 ± 19.9 ng/g), Cd (5.60 ± 9.04 μg/g), Hg (69 ± 41 ng/g) and Pb (5.0 ± 3.5 μg/g) were also detected.     

Heavy metal accumulation by selected plant species along the national highway: a case study of Udaipur,Rajasthan, India

ABSTRACT

A detailed research was conducted to find out the heavy metal accumulation by plant species at the roadside. Bioconcentration, bioaccumulation and translocation factors were estimated in 10 individuals of each investigating plant species. The plant and soil samples used in the research were collected along the National Highway-76 from Chittorgarh to Udaipur, Rajasthan, India. The concentration of cadmium and lead in roadside soil, plant roots, stems and leaves shows a correlation. The highest bioconcentration factor of Cd and Pb was 0.22 ± 0.04 and 0.13 ± 0.02 estimated in Bougainvillea spectabilis Willd. The highest translocation factor of Cd was 1.30 ± 0.50 in Pongamia pinnata L., and the highest translocation factor of Pb was 1.63 ± 0.45 estimated for Nerium oleander L. The average concentrations of Cd and Pb were 11.35 ± 1.60 and 223.70 ± 68 mg kg^?1 in investigated roadside soil. The average concentrations of accumulated Cd and Pb in B. spectabilisWilld. were 2.38 ± 0.49, 1.97 ± 0.51, 3.07 ± 0.78 and 29.34 ± 7.82,18.96 ± 5.62, 37.75 ± 12.93 mg kg^?1 in roots, stems and leaves, respectively. The decreasing order of bioaccumulation factor of cadmium in plants was B. spectabilis Willd.>Butea monosperma (Lam.) Taub>Calotropis procera (Ailton) Dryand>N. oleander L.>P. pinnata L. The decreasing order of bioaccumulation factor of lead in plants was B. spectabilis Willd.>P. pinnataL.>B. monosperma (Lam.) Taub>C. procera (Ailton) Dryand>N. oleander L. The B. spectabilis Willd. was identified as a rhizofiltration tool of heavy metals such as Cd and Pb with higher bioconcentration factor. P. pinnata L. for Cd and N. oleander L. for Pb were revealed for phytoextraction technology with high translocator factor to accumulate and eliminate these toxic elements from soil.     

Elemental Analysis of Phytotherapeutic Products by Inductively Coupled Plasma–Tandem Mass Spectrometry

A procedure for the determination of As, Cd, Cr, Ni, Pb, and V in phytotherapy medicines by inductively coupled plasma–tandem mass spectrometry is reported. The use of tandem mass spectrometry with oxygen into an octopole reaction system at various gas flow rates and the combination of on-mass and mass-shift modes was evaluated. Cadmium, Cr, Ni, and Pb were determined as free atomic ions while As and V were determined as the oxides AsO⁺ and VO⁺ in the same run. Samples were prepared by microwave-assisted digestion with dilute nitric acid and hydrogen peroxide. Two plant-certified reference materials (apple leaves and tomato leaves) were used to check the accuracy. For tandem mass spectrometry with 0.5?mL min^?1 O₂, recoveries in the 85–113% were typically obtained and no statistical differences were observed at the 95% confidence level (t-test) in comparison with the certified values. Using these conditions, the limits of detection for the method were 0.01, 0.0002, 0.008, 0.008, 0.003, and 0.002?µg g^?1 for As, Cd, Cr, Ni, Pb, and V, respectively. The procedure was used for the analysis of four phytotherapic drugs and the determined concentrations were up to 0.168?µg g^?1 As, 0.03?µg g^?1 Cd, 0.82?µg g^?1 Cr, 1.18?µg g^?1 Ni, 0.52?µg g^?1 Pb, and 2.4?µg g^?1 V with average precision values of 8% as the relative standard deviation. The found concentrations were compared with limits proposed in official guidelines and, in most cases, the values were below the maximum limits allowed.     

Certification of the contents of some heavy metals (Cd, Cu, Hg, Ni, Pb and Zn) in three types of soils

Summary The element contents of Cd, Cu, Hg, Ni, Pb and Zn of three types of soil were certified. The preparation, homogeneity and stability are reported. The certified contents as well as values for Co, Cr, Mn and Se and for the aqua regia soluble contents Cd, Cr, Cu, Mn, Ni, Pb and Zn are given.

---

Zertifizierung von Schwermetallspuren (Cd, Cu, Hg, Ni, Pb und Zn) in drei Bodenproben

Zusammenfassung In drei verschiedenen Bodenproben wurden die Elementgehalte an Cd, Cu, Hg, Ni, Pb und Zn zertifiziert. Es wird berichtet über die Bereitung, Homogenität und Stabilität. Die zertifizierten Gehalte sowie der Gehalt an Cr, Co, Mn und Se und der Gehalt an königswasserlöslichem Cd, Cr, Cu, Mn, Ni, Pb und Zn werden angegeben.

     

Preparation, characterization, and application of a new thiol-functionalized ionic liquid for highly selective extraction of Cd(II)

A highly selective thiol-functionalized ionic liquid (thiol-FIL) was synthesized and characterized by FT-IR and ESI mass spectroscopy. The capability of thiol-FIL to extract Cd(II), Ni(II), Cr(III) and Pb(II) was evaluated. It is found that thiol-FIL possesses high selectivity for Cd(II), and this has led to a method for determination of Cd(II) by flame atomic absorption spectrometry that is free of interferences by up to a 1,000-fold excess of Na(I), Mg(II), Ca(II), Mn(II), Fe(III), Al(III), Cu(II), Zn(II), Ni(II), Cr(III), Co(II), As(III), Pb(II), and Hg(II). With extraction equilibrium time of 1 min, a good linearity (r = 0.9998) and a detection limit of 0.39 μg?L^?1 were obtained. The precision (RSD) for 11 replicate measurements of 10 μg?L^?1 Cd was 1.6%. The method was validated using certified reference materials. The recoveries of cadmium in spiked real samples ranged from 97% to 102%.     

Elemental Analysis and Metal Intake of Romanian Vegetables

ABSTRACT

Inductively coupled plasma-mass spectrometry multielemental profiling was performed to determine eight elements in 54 vegetable samples. The range of concentrations of Fe and Ni was 1.91?±?0.09 to 443.31?±?22.32?mg/kg and 0.05?±?0.004 to 16.36?±?0.36?mg/kg, respectively. The concentrations of Pb and Cd were up to 1.56?±?0.04 and 0.78?±?0.04?mg/kg, respectively. Some samples exceeded the maximum admissible limits imposed by national and international regulations. The mean concentrations of Mn and Cu were between 20.93?±?0.43 and 13.98?±?0.30?mg/kg in tomatoes and 20.60?±?0.53 and 11.25?±?0.22?mg/kg in peppers. For the evaluation of health risk related to the consumption of vegetables, the daily intake rate, target hazard quotient (THQ), and hazard index were evaluated. The daily intakes were low and correspond to 2 to 14% of the tolerable daily values established by legislation. The results showed that the THQ and hazard index for the metals were lower than 1, indicating that the vegetable ingestion does not represent a significant risk for consumer health. Analysis of variance revealed that Zn may be used as a species-specific marker (p?=?0.026). Principal component analysis extracted three main components, explaining a total variance of 72.49% and grouped all determined elements.     

Potentiometric Studies of Some Bivalent Metal Ion Complexes of a New Ligand,o-(2-Thiazolylazo)-4-Ethylphenol

Abstract

The complexations of a new ligand, o-(2-thiazolylazo)-4-ethylphenol(TAEP) with Ca(II), Mn(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II), Hq(II) and Pb(II) have been studied by potentiometric titrations, at 25.0 ± 0.2°C and an ionic strength of 0.1 in 30% v/v dioxane-water mixture. The dissociation constant and spectral data of TAEP and formation constants of the complexes containing various molar ratios of metal ion to ligand, are reported. It is observed that Ca(II) forms only an ML complex in any molar ratios, whereas other metal ions react in two steps forming ML and ML₂ complexes in a 1:3 molar ratio. In the case of 1:1 and 1:2 molar ratios, Mn(II), Co(II), Cd(II) and Hg(II) seemed to form bi- or poly-nuclear complexes because of slightly different formation curves from those of 1:3 molar ratio. The sequence of the first successive formation constant is Cu > Hg > Ni > Pb > Co > Zn > Cd > Mn > Ca, showing Mellor-Maley's order. Further correlation is shown between the formation constants and the second ionization potentials of the metals.