Assessment of metal contamination in an urban drainage system (using water and tilapia, Oreochromis spp.) in view of human health effect. A case study of some selected communities in Cape Coast township in Ghana

This research work aimed at studying the metal content of water and tilapia fish sample, Oreochromis spp., from a wastewater-fed pond around the University of Cape Coast community using instrumental neutron activation analysis. The metals studied were Al, As, Ca, Co, Cr, Cu, Fe, K, Mg, Mn, Na, V and Zn. In the water samples the order of elemental concentrations at sampling point 1, in ??g/g, was K (75.96?±?0.92), Na (18.52?±?0.35), Al (6.00?±?0.89), Mn (3.28?±?0.44), As (3.08?±?0.40), Mg (1.56?±?0.17), Ca (0.70?±?0.08), Cu (0.54?±?0.08) and V (0.04?±?0.01). Co, Cr, Fe and Zn were below detection limits of INAA. The order of elemental concentrations in the water at point 2 was as follows: Na (4.99?±?0.14), K (4.82?±?0.89), Mn (4.40?±?0.53), Mg (2.92?±?0.37), Al (1.98?±?0.21), As (0.69?±?0.10), Ca (0.24?±?0.07) and V (0.23?±?0.06) with Co, Cr, Cu, Fe and Zn falling below the detection limit of INAA. The concentrations recorded for Al, As, Cu and Mn in the water samples were all above WHO permissible limits. The mean levels of heavy metals in the soft tissue of tilapia was of the order: K?>?Mg?>?Fe?>?Ca?>?Na?>?Al?>?Mn?>?Zn?>?V?>?Cu?>?Cr?>?Co. Arsenic was below detection limit. The transfer factor values calculated for the metals Al, Ca, K, Mg, Mn, Na and V were all greater than one indicating movement of metals from the water column to the tilapia species. The hazard index (HI) calculated for Al, Fe, Mn and V suggested possible occurrence of adverse health effects (HI?>?1) where as the HI value obtained for Cr, Cu and Zn (i.e., HI?<?1) suggested unlikely adverse effects occurring.     

Trace metal accumulation in tissues of sole (Solea senegalensis) and the relationships with the abiotic environment

The distribution patterns and the organ-specific accumulation trends of 10 trace metals (iron, manganese, zinc, copper, chromium, nickel, cobalt, lead, cadmium and silver) and 4 major elements (sodium, potassium, calcium and magnesium) in 10 different tissues (heart, muscle, kidney, stomach, intestine, liver, gill, gonads, white skin and dark skin) of a benthic fish species (Solea senegalensis) from a densely populated coastal area affected by anthropogenic activities, the Bay of Cadiz (SW Spain), have been investigated. High variability of metal concentrations among tissues were found for Ca, Fe, Zn, Cu, Pb and Ag. Factor analysis was applied to study this variability. Five principal components were found explaining the 92.95% of the total variance and similarities in behavioural patterns of bioaccumulation were described. They associated Mg, Cr, Ni and Mn to intestine and stomach tissues (PC1), Ag, Cu and Cd to liver (PC2), Zn, K and Co to gonads (PC3), Na, Fe and Pb to gill, heart and kidney tissues (PC4) and Ca, Pb and Mn to gill and dark skin (PC5). The metallic concentration in the sediment and water was also studied. The pollution in this area was found moderate with outstanding values of Zn, Cu and Pb (average values of 139, 50.4 and 75.6?mg?kg^?1, respectively) in sediment and dissolved Cu (average value of 2.5?µg?L^?1). Metal bioconcentration trends followed the order Zn?>?Cu?>?Cd?>?Pb for dissolved metals in seawater, Cu?>?Zn?>?Cd?>?Pb?≈?Mn?>?Fe?≈?Ni?≈?Co for metals associated to particulate matter and Zn?≈?Cu?>?Cd?>?Mn?>?Co?≈?Fe?>?Ni?≈?Pb?>?Cr for metals in the sediment. Higher values were found for copper in liver, zinc in gonads and lead in gill, showing the relationship between biotic and abiotic environment. In addition, Cd bioconcentration factors were found high in liver and gill showing the sensitivity of sole to this metal even at low concentrations.     

Chemometric Assessment of the Interactions Between the Metal Contents,Antioxidant Activity,Total Phenolics,and Flavonoids in Mushrooms

The elemental composition and antioxidant activity have been obtained for regional mushrooms species, wild and cultivated, from Dambovita County, Romania. A multivariate approach and data mining techniques (principal component analysis and cluster analysis, respectively) were applied in order to evaluate the correlation matrix for these parameters for both caps and stipes of mushrooms. The associations between metallic elements (i.e., Fe, Cu, Cd, Pb, Co, Ni, Zn, Mn, Cr, Na, K, Ca and Mg) correlated with antioxidant activity, total phenolics, and total flavonoids were carried out by using a full factorial linear design. The multivariate functional analysis revealed on associated accumulation of several elements in mushrooms. In the cluster analysis, the dataset was treated to appreciate the correlation between metals group (e.g., heavy metals, such as Fe, Cu, Cd, Pb, Co, Ni, Zn, Mn, Cr, and important nutritional elements, such as Na, K, Ca, and Mg). Fungal species with similar characteristics in terms of metal accumulation formed two distinctive clusters. From a point of view of the consumer, the content of Cd and especially Pb in the fruiting bodies of the analyzed mushrooms species may be considered elevated, so that mapping the risk is compulsory. Applying the chemometric tools in the sense mentioned above, as well as in helping the scientific research by optimizing the number of data points, was shown to be extremely useful.     

Elemental Analysis of Edible Mountain Nettle (Obetia tenax) and the Influence of Soil on Its Chemical Composition

In developing countries, the dietary intake of essential elements is largely dependent on the consumption of edible fruits and leafy vegetables. The distribution of elements in the indigenous edible plant, Obetia tenax (mountain nettle), was investigated as a function of soil quality from eight sites in KwaZulu-Natal, South Africa. The results show concentrations of elements in the leaves to be in decreasing order of Ca?>?Mg?>?Fe?>?Mn?>?Zn?>?Cr?>?Cu?>?Ni?>?Pb?>?Co?>?As?>?Cd?>?Se, and in the stems and roots to be in decreasing order of Ca?>?Mg?>?Fe?>?Mn?>?Zn?>?Cu?>?Ni?>?As?>?Pb?>?Co?>?Cd?>?Cr?>?Se. The quality and pollution status of soil was evaluated by geoaccumulation indices and enrichment factors, which indicated moderate cadmium contamination at the Msinga location that was confirmed by the pollution index and ecological risk levels of single-factor pollution. An assessment of overall contamination of soil using Nemerow pollution index showed moderate pollution by cadmium, while the potential toxicity index indicated low-grade risk for all elements at all sites. Principal component and cluster analysis revealed two groups of elements with similarities, As, Cd, Co, Cr, Cu, Mn, Ni, and Fe, suggesting a lithogenic source and an anthropogenic source for Pb and Zn. Correlation analysis showed significantly positive correlations between As, Co, Cr, Cu, Fe, and Ni/Cd in the soil, confirming the elements’ common origin.     

Determination of macro and trace elements in canned marine products by inductively coupled plasma—optical emission spectrometry (ICP-OES) and ICP—mass spectrometry (ICP-MS)

This study determined the concentration of eight macroelements (Na, K, Mg, P, S, Ca, Fe, Zn) and nineteen trace elements (Li, Be, Cr, Mn, Co, Ni, V, Cu, Ga, Se, Rb, Sr, In, Sn, Cs, Ba, Tl, Bi, U) in commonly consumed canned marine products from South Korea. The samples were wet-digested using nitric acid and hydrogen peroxide by a microwave system and analyzed for macroelements using inductively coupled plasma—optical emission spectrometry (ICP-OES) and for trace elements by inductively coupled plasma—mass spectrometry (ICP-MS). The analytical methods were validated by the correlation coefficients, limits of detection and quantification, correlation variance, spiking recovery tests, and analyzing a NIST 1566?b oyster tissue certified reference material. The concentrations of macro and trace elements varied among the canned marine products. The macroelements were present in the order of Na?>?K?>?P?>?S> Mg?>?Ca?>?Fe?>?Zn. In general, the concentrations of macro and trace elements were within the specified limits of Food and Nutrition Board, Joint Food and Agriculture Organization/World Health Organization Expert Committee on Food Additives, and Ministry of Food and Drug Safety, Korea. The results suggest that the analyzed canned marine products are safe in terms of the analyzed elements and their consumption therefore does not cause any threat to human health.     

Molybdenum(VI) Oxide-Modified Silica Gel as a Novel Sorbent for the Simultaneous Solid-Phase Extraction of Eight Metals with Determination by Flame Atomic Absorption Spectrometry

A silica-based inorganic sorbent was synthesized by the thermal decomposition of ammonium heptamolybdate on silica and applied for the preconcentration and simultaneous determination of Cd, Co, Cr, Cu, Fe, Mn, Ni, and Pb in river water samples using a column system with flame atomic absorption spectrometry. Attenuated total reflection-Fourier transformation infrared spectroscopy, scanning electron microscopy, and electron dispersive spectroscopy were used for sorbent characterization. The effects of pH, sample volume, eluent type, eluent concentration, eluent volume, sample flow rate, and matrix ions (Al, Bi, Ca, Mg, and Zn) on the recovery of the metals in model solutions were investigated. The adsorption capacities (µmol g^?1) of SiO₂-MoO₃ were 88.96 (Cd), 169.69 (Co), 153.85 (Cr), 188.88 (Cu), 179.05 (Fe), 163.81 (Mn), 136.31 (Ni), and 38.61 (Pb). The detection limits of the method were 9.09, 10.82, 10.77, 49.57, 31.64, 6.40, 8.86, 19.15?µg L^?1 for Cd, Co, Cr, Cu, Fe, Mn, Ni, and Pb, respectively, with a preconcentration factor of 25. The developed method was used for the determination of the target metals in real samples and the recoveries for spiked samples were found to be from 91.2% to 102.9%.     

Mineral constituents of edible parasol mushroom Macrolepiota procera (Scop. ex Fr.) Sing and soils beneath its fruiting bodies collected from a rural forest area

Concentrations and interrelationships of twenty elements were studied in parasol mushroom and in the top layer of soil (0–10 cm) from the area of Kiwity (Poland). K, P, Mg, Ca, and Zn were found to be the most abundant elements in the mushroom. Higher concentrations of Fe, Mn, Na, Ni occurred in stipes then in caps, while Cd, Cr, Cu, Hg, Rb dominated in caps. Ag, Al, and Ba concentrations in caps and stipes were similar. Parasol mushroom is efficient in up-take and separation of Ag, Cd, Cu, Hg, K (in caps, the bioconcentration factor is BCF ≥ 100), Na, P, Rb (50 < BCF < 100), and Mg, Zn (BCF > 10) in its fruiting bodies, while Al, Ba, Ca, Co, Cr, Fe, Mn, Sr, and Pb are eliminated (BCF < 1). Parasol mushroom from rural forest area in the north-eastern region of Poland is of hygienic concern for human health because of toxic mercury and cadmium content in the edible caps, which are also rich in essential Cu, Fe, and their K, Mn, and Zn content is also high.     

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.     

Determination of minor, trace and toxic elements in chewing tobacco products by instrumental neutron activation analysis and identification of glutamic acid

Tobacco smoking/chewing has been a cause of concern because of it being related with oral cancer. It causes stimulation and ill physiological effects. Ten different brands of spit tobacco, eight gutkaas and five paan masalas have been analyzed for seven minor (Al, Na, K, Ca, Cl, Mg, and P) and 17 trace (As, Ba, Br, Co, Cr, Cs, Cu, Eu, Fe, Hg, La, Mn, Rb, Sb, Sc, Th, and Zn) elements by instrumental neutron activation analysis. Also Ni and Pb were determined by atomic absorption spectrophotometry. Concentration of Cd was below detection limit (<10?mg?kg^?1) in the tobacco samples. Mg, generally added as MgCO₃ to prevent caking, is present as minor constituent in spit tobacco and gutkaas but is below detection limit (<1?g?kg^?1) in paan masalas. Most elemental concentrations vary in a wide range depending on the nature of chewing tobacco. Spit tobacco has been found to be more enriched in essential elements (Ca, K, Na, P, Mn, and Rb), whereas gutkaas contain higher concentrations of Fe, Cr, Cu, and Zn. Paan masalas contain lower contents of other elements but higher content of Hg. Gutkaas also contain higher amounts of As and Pb. Further glutamic acid has been separated from tobacco leaves and characterized as it might bind with some elements.     

Elemental Analysis and Nutritional Value of Seaweed from the East Coast of KwaZulu-Natal,South Africa

Seaweed, biologically and phycologically referred to as algae, is classified as Rhodophyta (red), Chlorophyta (green), and Ochrophyta (brown). In this study, the concentrations of 13 elements (As, Ca, Cd, Co, Cr, Cu, Fe, Mg, Mn, Ni, Pb, Se, and Zn) were investigated for 14 seaweed species of varying classes (Amphiroa bowerbankii, Ceramium virgatum, Dichotomaria tenera, Ellisolandia (Coralline) elongata, Gelidium abbottiorum, Gracilaria canaliculata, Jania rubens, and Jania (Haliptylon) squamata of the Rhodophyta (red); Caulerpa filiformis, Codium capitatum, Halimeda cuneata, and Ulva rigida of the Chlorophyta (green); and Cystoseira myrica and Sargassum elegans of the Ochrophyta (brown) to determine the nutritional value of seaweed based on its medicinal properties, industrial importance, and natural abundance. The elemental distribution in seaweeds was in decreasing order of Ca?>?Mg?>?Fe?>?Cu?>?Mn?>?Zn?>?Cr?>?Co?>?Se?>?As?>?Pb?>?Ni?>?Cd. All edible species contained high levels of macro and microelements with the corali sp. accumulating high levels of Ca. Of the edible seaweeds characterized, only three (G. abbottiorum, E. (Coralline) elongate and C. virgatum) are suitable for human consumption due to high levels of As, Cd, and Pb present in the other species. These three species are also rich in essential nutrients, specifically C. virgatum, which is high in Cu and Se. Hierarchical cluster analysis showed a clear similarity in distribution of essential and toxic elements in similar classes of seaweed.     

电感耦合等离子体原子发射光谱法同时测定植物样品中多种元素

本文为环境样品分析建立了准确、灵敏、快速的分析方法,探讨了酸类及酸度对谱线强度的影响,同时对基体元素的谱线干扰进行了校正和背景扣除,测定了环境背景值样品树干和树叶中15种元素,经标样测定结果满意。     

Microwave digestion-ICP-MS for elemental analysis in ambient airborne fine particulate matter: rare earth elements and validation using a filter borne fine particle certified reference material

NIST standard reference material SRM 2783 was employed to validate a high temperature, high pressure, two-stage microwave assisted acid digestion procedure using HNO₃, HF and H₃BO₃ developed for the analysis of trace elements (including rare earths) in atmospheric fine particulate matter (PM_2.5) prior to inductively coupled plasma mass spectrometry (ICP-MS). This method quantitatively solubilized Na, Mg, Al, K, Ti, V, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Rb, Sb, Cd, Cs, Ba, Pb, Th, U and several rare earth elements (REEs) (La, Ce, Pr, Nd, Gd, Dy, Er, Sm and Eu) from SRM 1648 and SRM 2783. A small amount of HF in the first stage was required to dissolve silicates necessitating the corresponding addition of H₃BO₃ in second stage to dissolve fluoride precipitates of Mg, La, Ce and Th. The optimized microwave dissolution—ICP-MS method detected Na, Mg, Al, K, Ti, V, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Rb, Sr, Cd, Mo, Sb, Cs, Ba, La, Ce, Pr, Nd, Sm, Gd, Pb, Th and U at trace to ultra-trace levels in ambient airborne fine particles from three sites in North Carolina. La to light lanthanide signature ratios suggested that soil and motor vehicles are the dominant REE sources in SRM 2783 and PM_2.5 samples collected during this study.     

Determination of trace elements of some Egyptian crops by instrumental neutron activation,inductively coupled plasma-atomic emission spectrometric and flameless atomic absorption spectrophotometric analysis

Instrumental neutron activation analysis was used for the determination of Al, Br, Ca, Ce, Cl, Co, Cr, Cs, Eu, Fe, K, La, Mg, Mn, Na, Rb, Sb, Sc, Se, Ti, Th, V and Zn, ICP-AES for the determination Al, Ag, Ba, Be, Ca, Co, Cr, Cu, Fe, Ga, K, Li, Mg, Mn, Na, Ni, P, Sc, Sr, Ti, V and Zn and flameless AAS for the determination of Cd, Hg and Pb in egg plant, potatoes, green pepper (Leguminosae), vegetable marrow (Cucurbitaceae), pears, apple (Rosaceae), castor oil plant (Euphorbiaceae), lettuce (compositae), dill, parsley, coriander (Umbelliferae), and in some soil samples collected from Aswan province.     

An integrated approach to the complete chemical analysis of magnesium or sodium diuranate (yellow cake) sample

A procedure for the complete chemical analysis of magnesium or sodium diuranate (yellow cake) sample is reported. Uranium is determined gravimetrically after peroxide precipitation. Optimum parameters, such as pH, quantity of hydrogen peroxide, volume of sample, temperature and complexing agent for quantitave precipitation of uranium, and effective separation of other elements were studied. Aluminum, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, Pb, and Zn were determined by flame atomic absorption spectrometer and B, Mo, SO₄, REEs and Y by inductively coupled plasma atomic emission spectrometer in the filtrates of hydroxide and peroxide precipitation separation. The proposed method is accurate and the precision is characterized by an RSD of ~0.2% for U; 2 to 6% for Mg, Na, K, Ca, Fe, SiO₂, Al, Cd, Co, Cr, Fe, Mn, Ni, Pb, and Zn and 3 to7% for REEs, Y, Mo and B     

Determination of impurities in nuclear fuel element components by neutron activation analysis

Neutron activation analysis methods for the determination of impurities in zirconium cladding material and uranium oxide are described. Detection limits for the elements Al, Cd, Cr, Co, Cu, Hf, Fe, Mn, Ni, W and U in zirconium are below that required by the ASTM B 352-79 standard. The method has been tested on the NIST SRM 360a Zircaloy-2 from which the elements Na, Mg, Al, Ca, V, Cr, Fe, Co, Ni, Cu, Eu and U have been detected. The values for Cr, Fe, Ni and Cu are compared with the certified values. A method for the pre-irradiation separation of the elements Mg, Na, Al, K, Sc, Ca, V, Mn, Cr, Fe, Co, Cu, Zn, Rb, Zr, Cd, Cs, REE and Hf from uranium has been developed. A neutron activation analysis method for the determination of those elements in uranium is described. The method is tested by the analysis of the IAEA reference sample SR-54/64. The elements Al, Mn, V, Cu, Cr, Co, Ni and Fe have been detected and the results compared with the certified values.     

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%.     

藏药材白花龙胆花中微量元素的分析

对藏药材白花龙胆花中17种微量元素（Cu、Zn、Fe、Mn、Co、Ni、Se、Cr、Mg、Ca、K、Na、P、As、Hg、Pb、Cd）的含量作了测定。结果表明,白花龙胆花中含有较高的人体必需微量元素和常量元素,其中常量元素K、Ca、Na、Mg和微量元素Zn、Fe、Mn的含量均较高。     

Distribution of Minor and Trace Metals in Carezza Lake (ANTARCTICA) Ecosystem

Abstract

This paper reports the distribution of a series of metals in natural samples collected at Carezza Lake in Antarctica, during the Italian Expedition in the austral summer 1989/90. The considered elements are: water, sediments and soil sampled from the surroundings of the lake and algae. The determination of the total concentration of the following metals was performed: Al, As, Ca, Cd, Co, Cr, Cu, Fe, Mg, Mn, Na, Ni, Pb, Zn. In addition, for sediment and soil samples, a speciation study was performed for some metals, namely Cd, Co, Cr, Cu, Fe, Mn, Ni, Zn, using the Tessier procedure.     

Trace element profile of a wild edible mushroom (Suillus granulatus)

Seventeen elements, Al, Ca, Cd, Co, Cr, Cu, Fe, K, Li, Mg, Mn, Na, Ni, P, Pb, V, and Zn (macroelements and trace elements) were investigated by Atomic Spectrometries on a particular wild edible mushroom collected in the central region of Argentina during 2 different years in the same season. The metal content profile in Suillus granulatus samples is given. The found quantities of Na, K, Ca, Mg, Fe, P, V, and Al were 0.40, 10.84, 0.48, 0.30, 0.57, 4.24, 0.18, and 1.23 g/kg dry weight, respectively. The levels of Li, Cu, Zn, Cd, Co, Ni, Cr, and Mn were 0.98, 23.02, 22.30, 0.26, 0.16, 1.17, 0.90, and 28.75 mg/kg dry weight, respectively. Pb was not detected at the investigated levels. The results indicate that the levels of metals in the analyzed samples are not considered to be a health risk. In order to demonstrate the validity of our method, a recovery study was performed with acceptable results.     

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.