Evaluation of Sample Preparation Procedures for Determination of Cr(VI) in Cr2O3 Pigments by Vis Spectrophotometry

Abstract Six sample preparation procedures were evaluated for selective extraction of Cr(VI) from commercial samples of chromium oxide green (Cr2O3) pigments prior to formation of its diphenylcarbazone complex [CrDPCO]- for determination by visible spectrophotometry: (I) water-soluble chromium; (II) EPA method 3060A without Mg2+; (III) EPA method 3060A with Mg2+; (IV) Na3PO4 based extraction; (V) method IRSA16 based on acidic extraction and; (VI) Na2CO3 based extraction. Evaluation of the influence of concomitant Cr(III) ions, time and stability of the [CrDPCO]- complex was investigated. Recoveries of soluble and insoluble Cr(VI) species were 86% and 80%, respectively, using procedure (VI). Direct calibration against aqueous standards prepared in the extraction medium was successful for Cr(VI) in the concentration range 0.05-1.50 μg L-1. Limits of detection and quantitation were 0.3 µg g-1 and 1.0 µg g-1, respectively, for 250 mg subsamples/25 mL. Procedure (VI) was applied to the analysis of four commercial samples of Cr2O3 pigments, three determined to have Cr(VI) within compliance limits below 1.0 µg g-1, but one at 16.6 ± 0.6 µg g-1, prohibiting use of this pigment in cosmetic formulations. This sample was conveniently employed to evaluate the accuracy of the method. The recommended procedure is simple and accurate and has been adopted by Tecpar's laboratory of Parana Institute of Technology (Curitiba, Brazil).

Evaluation of Chromium and Manganese levels in sports supplements using graphite furnace atomic absorption spectrometry / Avaliação do teor de Cromo e Manganês em suplementos esportivos por meio de espectrometria de absorção atômica em forno de grafite

ABSTRACT Objective In this paper, we studied three different types of ordinary sports supplements containing whey protein: whey protein-based ones, hypercaloric ones, and protein bars. Methods A sample preparation procedure was studied employing microwave-assisted wet digestion in order to determine the Chromium and Manganese levels by graphite furnace atomic absorption spectrometry. Results The developed methods have presented good accuracy (recoveries in the range of 90% to 109%) and precision (Relative standard deviation <8%). Although an adequate detectability was obtained (50ng g-1 for Manganese and 65ng g-1 for Chromium), the sample preparation method was also adequate to inductively coupled plasma mass spectrometry analysis. The method was applied to 26 commercial samples, in which the Chromium concentrations were in the range between 0.22 and 1.0μg g-1 and the Manganese concentrations varied from 2.0 to 37μg g-1. Conclusion The results obtained by atomic absorption for both analytes were in agreement with those obtained by mass spectrometry. In addition, some samples presented concentrations of Chromium above the recommended daily intake and, as a result, we used the X-ray powder diffraction technique as an analytical tool to evaluate the oxidation state of Chromium in such samples.

RESUMO Objetivo Neste trabalho, foram estudados diferentes tipos de suplementos esportivos contendo proteína de soro de leite, conhecidos como: whey protein, hipercalóricos e barras de proteína. Métodos Um procedimento de preparo de amostras foi estudado com o emprego de digestão úmida assistida por micro-ondas, a fim de determinar os teores de cromo e manganês por espectrometria de absorção atômica em forno de grafite. Resultados Os métodos adotados apresentaram boa exatidão (recuperações na faixa de 90 a 109%) e precisão (Desvio padrão relativo <8%). Embora tenha sido obtida uma capacidade de detecção adequada de 50ng g-1 para o manganês e de 65ng g-1 para o cromo, o método de preparo da amostra também se revelou adequado para a utilização em análises por espectrometria de massas com plasma indutivamente acoplado. O método foi aplicado a 26 amostras comerciais, cujas concentrações de cromo variaram entre 0,22 e 1,0μg g-1, e de manganês entre 2,0 e 37μg g-1. Conclusão Os resultados obtidos por absorção atômica, para ambos os analitos, mostraram-se de acordo com aqueles obtidos por espectrometria de massas. Além disso, algumas amostras apresentaram concentrações de cromo acima da recomendação de consumo diário e, como resultado, a técnica de difração de raios-X em pó foi utilizada como ferramenta analítica para avaliar o estado de oxidação do cromo em tais amostras.

The importance of corrosion resistance test of cannulas in the quality control of hypodermic needles

According to Anvisa risk rating, hypodermic needles offer medium risk to the user's health. This study discussed the importance of the corrosion resistance test in tubes of hypodermic needles, in the product quality control. A review of cannulas of hypodermic needles was carried out according to ISO 9626:2003 and 9259:1997 ABNT NBR. For the results evaluation, a scale which classifies the extent of corrosion was adjusted. 174 samples of PNI needles from 17 States and 9 different record holders were analyzed. According to the methodology of ISO 9626:2003, 100% of the samples were considered satisfactory. However, in accordance with the methodology of ISO 9259:1997, 97.1% of the samples were rejected. Irregularities can lead to impairment of product quality, resulting in risks to the consumer's health. Since 2011 the product has undergone certification, so it is necessary to reflect on the importance of corrosion resistance testing and mandatory certification for health monitoring.

Comparison Between Nickel and Chromium Levels in Serum and Urine in Patients Treated with Fixed Orthodontic Appliances: A Longitudinal Study

Objective: To compare levels of nickel and chromium in serum and urine in orthodontic patients treated with fixed orthodontic appliances. Material and Methods: Nickel and chromium ion concentration were measured in serum and urine of twenty patients (12 females and 8 males, aged 17-28 years old) who had fixed orthodontic treatment using Coupled Plasma-Atomic Emission Spectroscopy. The samples were taken before treatment (Baseline), two months, and six months later during treatment. Data were analyzed using repeated ANOVA, Bonferroni post-hoc test, and paired t-tests. The level of significance was set at 5%. Results: Average serum nickel level changed from 6.420 ppb to 6.855 ppb. Average serum chromium level changed from 5.305 ppb to 5.505 ppb in 6 months. Average urinary nickel level changed from 5.320 ppb to 5.610 ppb. Average urinary chromium level changed from 5.370 ppb to 5.520 ppb in 6 months. There was a statistically significant difference in serum (p<0.001) and urinary chromium (p=0.007) levels between observation times. Conclusion: Orthodontic treatment might raise both urinary and serum nickel levels, but the differences were not statistically significant; the alterations in chromium levels were not consistent; nickel levels were higher in serum than in urine; chromium levels were higher in urine than in serum.

Avaliação dos níveis de cromo total em águas para consumo humano / Evaluation of total chromium levels in drinking water

Níveis elevados de cromo associados às águas naturais não são comuns, mas concentrações elevadas desse elemento, de ocorrência natural, têm sido relatadas nas águas subterrâneas de vários sistemas aquíferos, incluindo o Aquífero Bauru, SP, Brasil. Este fato está associado à ocorrência de rochas máficas/ultramáficas e às condições alcalinas e oxidantes. Neste estudo foi desenvolvido e aplicado um método para monitorar a concentração de cromo total em amostras de água da cidade de São José do Rio Preto. Esta cidade está localizada no estado de São Paulo, na região onde concentrações superiores ao limite estabelecido pela legislação brasileira (0,05 mg/L) foram detectadas em águas subterrâneas de poços de abastecimento. O cromo total foi determinado usando-se Espectrometria de Massas com Plasma Indutivamente Acoplado (ICPMS) em 104 amostras de água coletadas, entre 2013 e 2017, em diferentes pontos de distribuição (zona rural, residencial, distrito industrial, comercial, reservatório de distribuição e estação de tratamento de água), considerando-se 52 locais. Em 99 % das amostras as concentrações de Cr estavam acima do limite de quantificação calculado para o método (0,001 mg/L). E 15% apresentaram concentrações acima do limite de regulação na água potável (Portaria 2914/2011), sendo, portanto, consideradas impróprias para o consumo humano.

Elevated chromium levels in the natural waters are not common, but the high concentrations of naturally occurring Cr have been reported in the groundwater of several aquifer systems. This finding is linked with the occurrence of mafic/ultramafic rocks and associated with the alkaline and oxidizing conditions. This study aimed at monitoring the total chromium concentration in drinking water samples from São José do Rio Preto city. Cr concentrations higher than the limit established by the Brazilian Legislation (0.05 mg/L) were detected in the groundwater from the deep supply wells. Total chromium was determined by using an Inductively Coupled Mass Spectrometer (ICP-MS) in 104 samples collected from the public drinking water distribution networks in 52 sites, from 2013 to 2017. Cr concentrations above the method limit of quantification (0.001 mg/L) were found in 99% of the analyzed samples. Approximately 15% of the collected samples presented Cr in concentrations above the established legislation limit for drinking water (Ordinance 2914/2011), that should be considered as improper for consumption.

Medios de cultivo económicos para la producción de un biocatalizador a células enteras para el tratamiento de aguas residuales que contienen Cr(VI) / Economical fermentation media for the production of a whole cell catalyst for the treatment of Cr(VI)-containing wastewaters

The biotechnology sector is continually seeking sustainable and more economical bioprocesses. Fermentation media produced with cheap components or wastes reduce production costs. Moreover, if wastes are used, they contribute to avoid environmental pollution. In this work, microbial growth media based on molasses or acidified glycerol as carbon sources and fertilizer as nitrogen source were tested for the production of a whole-cell catalyst that could be used in Cr(VI)-containing wastewater treatments. Results showed that the highest biomass production yield was obtained with a medium containing acidified glycerol 5% v/v and fertilizer 0.6% v/v. The biomass produced using this medium was immobilized in calcium alginate beads and used as catalyst in the biotransformation of Cr(VI) into Cr(III). The catalyst could be efficiently used for 5 reduction cycles of 40 mg/l Cr(VI) each. Cr(III) retention assays were performed to determine whether Cr(III) could be retained by the catalyst avoiding its solubilization in the supernatants. The retention capacity of the catalyst at 32 °C and pH 3.0 was 3 mg Cr(III)/g. Both an alternative and economical fermentation medium is here proposed for the optimization of Cr(VI)-containing wastewater treatment.

El sector industrial biotecnológico continuamente busca bioprocesos más económicos y sustentables. El uso de medios de cultivo producidos con componentes de bajo costo o con residuos reduce el presupuesto global del proceso y, particularmente si se utilizan residuos, se contribuye, además, a evitar la contaminación ambiental. En este trabajo se probaron medios de cultivo basados en melaza de caña o glicerol ácido como fuentes de carbono y energía, y fertilizante como fuente de nitrógeno, para la producción de un biocatalizador que podría ser usado para el tratamiento de aguas residuales que contienen Cr(VI). Los resultados mostraron que el mayor rendimiento de producción de biomasa se obtuvo con un medio que contenía 5% v/v de glicerol ácido y 0,6% v/v de fertilizante. Utilizando este medio se produjo la biomasa suficiente para la biotransformación de Cr(VI) a Cr(III), luego de ser inmovilizada en alginato de calcio. El proceso pudo ser aplicado eficientemente durante 5 ciclos de reducción de 40 mg/l de Cr(VI) cada uno. Además, se realizaron ensayos de retención de Cr(III) para determinar si esta especie química podría ser removida de la solución por interacción con el biocatalizador. La capacidad de retención obtenida por el biocatalizador a 32 °C y pH 3 fue de 3 mg de Cr(III)/g. De esta manera, se propone un medio de cultivo alternativo y económico para la efectivización de un tratamiento de aguas residuales que contengan Cr(VI).

Chromium oxide (51Cr2O3 ) used as biological marker was not absorbed by fish / Óxido de crômio (51Cr 2O3 ), usado como marcador biológico, não é absorvido por peixe

The aim of this study was to evaluate the rate absorption of radio-labeled chromium oxide (51Cr2O3), used as biological marker in nutrition studies with Nile tilapia Oreochromis niloticus. An experimental diet with approximately 58 µCi of specific activity of the element was encapsulated and fed daily to 35 adult Nile tilapia; a group of 35 fish was used as control feeding on a basal diet. At the beginning of the experiment five fish from each group were randomly selected and blood samples were drawn from control (BC) and experimental fish (BE). Fish were then euthanized by anesthetic overdoses and samples of the liver tissue (LT), renal tissue (RT), stomach without content (S), intestine without content (I), gills tissue (GT), muscle tissue (fillet; MT), visceral fat (VF), content of the digestive tract (CTDE) and water aquarium were collected from the experimental fish. The procedure was repeated daily for one week. Simple linear regressions were adjusted - days of collection vs. determination coefficients, and were established for statistical comparisons of the measured activity of 51Cr readings in sampled blood and tissues (logarithmic transformation) for samples of the control and experimental fish. No differences (P>0.05) were detected between samples from BC fish and BE, RT, VF, MT and LT of treated fish, but samples of GT, I, S, CTDE and WA from the tanks holding fish which received the experimental diet differed from control (P<0.05). The experimental results indicate that the trivalent chromium in the form of 51Cr2O3 was not significantly absorbed by the gastrointestinal tract, gills or another possible route of absorption under these experimental conditions and with Nile tilapia. Therefore, this marker was shown to be inert and can be safely used in nutrition studies.

O objetivo deste estudo foi avaliar a taxa de absorção de radiomarcador óxido de crômio (51Cr2O3), utilizado como marcador biológico em estudos de nutrição, com tilápia-do-nilo Oreochromis niloticus. Uma dieta experimental com cerca de 58µCi de atividade específica do elemento foi encapsulada, e 35 adultos de tilápia foram alimentados diariamente; um grupo de 35 peixes foi usado como controle e alimentado com uma dieta basal. No início do estudo, cinco peixes de cada grupo foram selecionados aleatoriamente, e amostras de sangue foram coletadas dos peixes controle (BC) e experimentais (BE). Os peixes foram sacrificados por overdose de anestésicos, e amostras do tecido do fígado (LT), rins (RT), estômago sem conteúdo (S), intestino sem conteúdo (I), brânquias (GT), tecido muscular (filé; MT), gordura visceral (VF), conteúdo do trato digestivo (CTDE) e água do aquário (WA) foram coletadas somente dos peixes experimentais. O processo foi repetido diariamente durante uma semana. As regressões lineares simples foram ajustadas - dias de coleta versus coeficientes de determinação - e foram estabelecidas para comparações estatísticas da leitura das atividades medidas de 51Cr (transformação logarítmica) nas amostras dos peixes controle e experimentais. Não foram detectadas diferenças (P>0,05) entre as amostras BC dos peixes controle e BE, RT, VF , MT e LT dos peixes experimentais, mas as amostras de GT, I, S, CTDE e WA dos peixes que receberam a dieta experimental apresentaram diferença significativa em relação aos que receberam a dieta controle (P<0,05). Os resultados experimentais indicam que o crômio trivalente na forma de 51Cr2O3 não foi significativamente absorvido pelo trato gastrointestinal, pelas brânquias ou por outra via possível de absorção nessas condições experimentais e com tilápia do Nilo. Portanto, esse marcador demonstrou ser suficientemente inerte, o que torna seguro seu uso em estudos de nutrição.

Concentración de Hg, Pb, Cd, Cr y As en hígado de Carcharhinus limbatus (Carcharhiniformes: Carcharhinidae) capturado en Veracruz, México

Concentration of Hg, Pb, Cd, Cr and As in liver Carcharhinus limbatus (Carcharhiniformes: Carcharhinidae) captured in Veracruz, Mexico. Pollution by heavy metals in marine ecosystems in the Gulf of Mexico is one of the hardest conservation issues to solve. Sharks as top predators are bioindicators of the marine ecosystem health, since they tend to bioaccumulate and biomagnify contaminants; they also represent a food source for local consumption. Thus, the objective of this study was to study the possible presence of heavy metals and a metalloid in livers of Carcharhinus limbatus. For this, a total of 19 shark livers were taken from animals captured nearby Tamihua, Veracruz, Mexico from December 2007 to April 2008. 12 out of the 19 captured sharks were males, one was an adult female, three were juvenile males, and three juvenile females. Four heavy metals (Hg, Pb, Cd, and Cr) and one metaloid (As) were analyzed in shark livers using an atomic absorption spectrophotometry with flame and hydride generator. Our results showed that the maximum concentrations found were: Hg=0.69mg/kg, Cd=0.43mg/kg, As=27.37mg/kg, Cr=0.70mg/kg. The minimum concentrations found were: As=14.91mg/kg, Cr=0.35mg/kg. The Pb could not be determined because the samples did not have the spectrophotometer minimum detectable amount (0.1mg/kg). None of the 19 samples analyzed showed above the permissible limits established by Mexican and American laws. There was a correlation between shark size and Cr and As concentration (Pearson test). The concentration of Cr and As was observed to be higher in bigger animals. There was not a significant difference in heavy metals concentration between juveniles and adults; however, there was a difference between males and females. A higher Cr concentration was found in females when compared to males. None of the samples exceed the maximum limit established by the laws of Mexico and the United States of America. Much longer studies are needed with C. limbatus and other species caught in the region, in order to determine the degree of contaminants exposure in aquatic ecosystems and to identify potential health risks to consumers.

La contaminación de los ecosistemas marinos y costeros por metales pesados en el Golfo de México es uno de los problemas que afectan a los recursos naturales del medio acuático. Los tiburones por situarse en niveles tróficos superiores de la red alimenticia acumulan y magnifican cantidades considerables de contaminantes. Por esta razón, el objetivo de este trabajo fue determinar la concentración de cuatro metales pesados (Hg, Cd, Pb y Cr) y un metaloide (As) en el tiburón punta negra (Carcharhinus limbatus) por medio de espectrofotometría de absorción atómica con flama y generador de hidruros. Se muestrearon 19 hígados de tiburones capturados cerca de Tamiahua, Veracruz entre noviembre 2007 y marzo 2008, de los cuales 12 fueron machos adultos, una hembra adulta, tres machos jóvenes y tres hembras jóvenes. Las concentraciones máximas registradas para cada metal fueron: Hg=0.69mg/ kg, Cd=0.43mg/kg, As=27.37mg/kg, Cr=0.35mg/kg. El Pb no fue detectado, no al menos la cantidad mínima de detección requerida por el espectrofotómetro de absorción atómica (0.1mg/kg). Ninguna de las muestras analizadas rebasó los límites máximos permisibles por las leyes mexicanas y americanas.

Nickel and chromium levels in the saliva of a Saudi sample treated with fixed orthodontic appliances

The aim of this study was to measure the amount of nickel [Ni] and chromium [Cr] released into the saliva of Saudi patients treated with fixed orthodontic appliances. Ninety salivary samples were collected in a cross-sectional manner. Forty samples were collected from patients [17 males, 23 females] with fixed orthodontic appliances after different periods of orthodontic treatment ranging from the first month and up to 32 months into treatment. The fixed orthodontic appliance consisted of 4 bands, 20 stainless steel brackets, and upper and lower nickel titanium or stainless-steel arch wires. The other 50 samples were collected from people without appliances [24 males, 26 females]. Samples were analyzed using Inductive Coupled Plasma/Mass Spectrometry and Inductively Coupled Plasma Optical Emission Spectroscopy to measure Ni and Cr levels, respectively. Student's t-test was used to compare Ni and Cr levels in the treated and untreated control groups. The mean Ni level was 4.197 microg/L in the experimental group and 2.3 ug/L in the control group [p < 0.05]. The mean Cr level was 2.9 microg/L in the experimental group and 3.3 microg/L in the control group [p < 0.05]. Fixed orthodontic appliances resulted in a non-toxic increase in salivary levels of Ni, but no change in Cr levels. Duration of orthodontic treatment did not affect Ni and Cr levels in the saliva

Effect of denture cleansers on metal ion release and surface roughness of denture base materials

Chemical disinfectants are usually associated with mechanical methods to remove stains and reduce biofilm formation. This study evaluated the effect of disinfectants on release of metal ions and surface roughness of commercially pure titanium, metal alloys, and heat-polymerized acrylic resin, simulating 180 immersion trials. Disk-shaped specimens were fabricated with commercially pure titanium (Tritan), nickel-chromium-molybdenum-titanium (Vi-Star), nickel-chromium (Fit Cast-SB Plus), and nickel-chromium-beryllium (Fit Cast-V) alloys. Each cast disk was invested in the flasks, incorporating the metal disk to the heat-polymerized acrylic resin. The specimens (n=5) were immersed in these solutions: sodium hypochlorite 0.05%, Periogard, Cepacol, Corega Tabs, Medical Interporous, and Polident. Deionized water was used as a control. The quantitative analysis of metal ion release was performed using inductively coupled plasma mass spectrometry (ELAN DRC II). A surface analyzer (Surftest SJ-201P) was used to measure the surface roughness (µm). Data were recorded before and after the immersions and evaluated by two-way ANOVA and Tukey's test (α=0.05). The nickel release proved most significant with the Vi-Star and Fit Cast-V alloys after immersion in Medical Interporous. There was a significant difference in surface roughness of the resin (p=0.011) after immersion. Cepacol caused significantly higher resin roughness. The immersion products had no influence on metal roughness (p=0.388). It could be concluded that the tested alloys can be considered safe for removable denture fabrication, but disinfectant solutions as Cepacol and Medical Interporous tablet for daily denture immersion should be used with caution because it caused greater resin surface roughness and greater ion release, respectively.

Desinfetantes químicos são normalmente associados a métodos mecânicos para remover manchas e reduzir a formação do biofilme. Este estudo avaliou o efeito de desinfetantes na liberação de íons metálicos e na rugosidade superficial do titânio comercialmente puro, ligas metálicas e resina acrílica termopolimerizável, simulando 180 ensaios de imersões. Espécimes em formato de discos foram confeccionados com titânio comercialmente puro (Tritan), liga de níquel-cromo-molibdênio-titânio (Vi-Star), liga de níquel-cromo (Fit Cast-SB Plus) e liga de níquel-cromo-berílio (Fit Cast-V). Os espécimes (n=5) foram imersos nestas soluções: hipoclorito de sódio a 0,05%, Periogard, Cepacol, Corega Tabs, Medical Interporous e Polident. Como controle, foi utilizada a água deionizada. A análise quantitativa de liberação de íons metálicos foi realizada por meio de espectrometria de massa com plasma indutivamente acoplado (ELAN DRC II). O rugosímetro (Surftest SJ-201P) foi utilizado para medir a rugosidade superficial (µm). Os dados foram registrados antes e depois das imersões e avaliados por ANOVA com dois fatores e teste de Tukey (α=0,05). A liberação de níquel provou ser mais expressiva nas ligas Vi-Star e Fit Cast-V após a imersão em Medical Interporous. Houve diferença significante na rugosidade superficial da resina (p=0,011) após a imersão. O Cepacol causou maior rugosidade superficial de forma significativa. Os produtos de imersão não influenciaram nos resultados da rugosidade do metal (p=0,388). Pode-se concluir que as ligas metálicas testadas podem ser consideradas seguras para a fabricação de próteses removíveis, mas as soluções desinfetantes como o Cepacol e a pastilha Medical Interporous para a imersão diária da prótese devem ser utilizados com cautela, pois causaram maior rugosidade superficial da resina e maior liberação de íons, respectivamente.

Evaluation of Viola betonicifolia for its nutrition value

In the present study, Viola betonicifolia [whole plant] and solvent fractions obtained thereof were evaluated for various micronutrients such as lead, copper, chromium, iron, nickel, zinc, cadmium, cobalt and macronutrients such as sodium, potassium and calcium using atomic absorption spectrophotometer and flame photometry respectively. It was observed that cobalt and cadmium were not detectible in tested samples while remaining nutrients were present in variable concentrations. The concentrations of all metals were compared with the recommended limits for plants and the daily consumption of all the nutrients were calculated on the basis of dose [15 g/70 kg/day or 214 mg/Kg body weight] prescribed by hakims in their practice. The concentration of chromium was far beyond the recommended limits in almost all the samples. Proximate analysis was carried out in the powdered form of the plant. Viola betonicifolia appeared as a good source of life essential nutrients like fats [18.70%], proteins [15.70%], carbohydrates [21.42%], fiber [39.01%] and vitamin C [150 mg/100 g]. In conclusion, Viola betonicifolia is an excellent source of various micro and macronutrients for human being and can be used safely as a nutritional supplement

Determination of Pb,Cd,Cr and Ni concentration in Imported Indian Rice to Iran

Heavy metal pollution has always been a major cause contamination of environment and considered as a major concern for food health. Rice is the most popular food among Iranians and presence of heavy metals in trace level in rice has received special attention because they are directly related to health. The aim of this research was to investigate the concentration of Pb, Cd, Cr, Ni in rice prevalent in the market of Iran. 20 of the most widely consumed brands of Iranian rice were purchased from local market in Iran. 3 samples of each brand were collected and certain volumes of each sample were digested with acid. Heavy metal contents in the digested samples were determined by atomic absorption spectrometry. The results showed that mean concentration Pb, Cr, Ni in rice samples respectively was 0.387, 0.683, 0.019 [mg/kg]. Notably the Ni and Cr content in the rice samples was found to be below the food sanitary standards in India rice. In the other hand 50% samples content Pb was found to be upper the food sanitary [Pb: 0.3 mg/kg]. The result indicated that weekly intake of heavy metal by rice was below the provisional tolerable weekly intake recommended by WHO/FAO. However, risk assessments needs considerable attention and better prevention this low pollution

Risk assessment of some heavy metals in edible chicken giblets

A total of 60 random samples of edible chicken giblets were collected from different markets in Kafr El-Sheikh governorate, Egypt, to evaluate their levels of some heavy metals as Lead, Copper, Zinc and Chromium. The obtained results indicated that the mean values of Lead, Copper, Zinc and Chromium concentrations in liver chicken samples were 0.47 +/- 0.08, 5.13 +/- 0.59, 5.27 +/- 0.59 and 0.38 +/- 0.08 mg/kg, respectively. While these concentrations in gizzard chicken samples were 0.24 +/- 0.06, 3.57 +/- 0.45, 3.15 +/- 0.39 and 0.22 +/- 0.06, respectively. Also these concentrations in heart chicken samples were 0.09 +/- 0.024, 1.77 +/- 0.26, 2.23 +/- 0.26 and 0 [not detected]. So these obtained data were compared with the permissible limits of [FAO/WHO, 1884] and [Egyptian Standard, 1993] and the public health risk of such toxic heavy pollutants metals was discussed

Bioremediation of chromium contaminated soil by Pseudomonas fluorescens and indigenous microorganisms.

Chromium is one of the toxic and hazardous pollutants in industrial wastewaters leading to soil contamination. In this study, the feasibility of remediating chromium contaminated soil using indigenous microorganisms and Pseudomonas fluorescens was evaluated. The contaminated soil sample was collected from Vellore and the pH, moisture content and chromium content were found to be 8.4, 22.5% and 5.1 mg/kg respectively. The effect of chromium on engineering properties showed decrease in permeability by 45.15%. For Pseudomonas fluorescens, the optimum pH, moisture content, biomass concentration and carbon source were found as 6.5, 20%, 10 mL and 10 mL/100 g respectively and for isolated mixed culture, the optimum parameters were found as 8.4, 25%, 15 mL and 15mL / 100 g respectively. Under optimum conditions, the reactor study showed 71.7% chromium reduction after 20 days. From the study, the bioremediation of chromium-contaminated soil by indigenous microorganisms was found to be a promising solution and after bioremediation, the engineering properties of the soil were found to be improved.

Batch adsorption studies for chromium removal.

The adsorption of hexavalent chromium (Cr (VI)) on pongamia (Pongamia pinnata) leaf powder was investigated in the present study. Crude pongamia leaf powder (CPLP) and nitric acid treated pongamia leaf powder (APLP) were used as adsorbents. CPLP did not show remarkable adsorption efficiency but APLP had good adsorption capacity and adsorption removal efficiency. The parameters studied included the contact time, initial solute concentration and pH. The optimum pH for removal of chromium was found to be 2 for both CPLP and APLP. The best contact time for maximum chromium adsorption was 165 minutes for CPLP and APLP. CPLP and APLP showed good adsorption capacity and adsorption removal efficiency at an initial chromium concentration of 5 mg/L. The adsorption was found to follow Langmuir and Freundlich isotherms for CPLP and APLP but they showed good curve fit for Freundlich isotherm.

Water pollution of oued msn a under catchments, in Algerian Tiaret region

This work concerns with the evaluation of the hydrous pollution evaluation of Industrial effluents, in the principal manufacturing units of Tiaret industrial park, as well as in the receiving dam of worn water of this city. Collected data were treated by correspondent factorial analysis between sites and sampling periods, in summer and winter. This analysis made us possible to focus obvious signs of pollution with the following evolutionary tendencies: On the level of Giplait: We have recorded an increase in the COD and the BODS during the two periods of sampling, as well as increasing rate of suspended solids. On the level of Sotrefit: We have recorded a strong phosphates concentration during the summer and winter periods, as well as a raised rate of Chromium [in winter] and Copper [in summer]. On the level of the ENF: We have noted that heavy metals prevail in these site effluents. On the level of the Barrage: We have noted a high concentration of nitrates, organic matter and suspended matter, as a source of pollution of the dam, which is currently used for the supply drinking water in Tiaret region. This work proved that Tiaret region become polluted

Removal of chromium from tannery industry effluents with (activated carbon and fly ash) adsorbents.

Adsorption is a strong choice for removal operations as it is very simple to recover a high quality product from waste sludge. The efficiency of adsorbents like fly ash and activated carbon are tested based on their performance to remove chrome at various pH values, bed heights, and concentration of adsorbents. The removal efficiency was also tested for wastewater characteristics in a pilot plant in addition to the use of adsorbents. The concentration of chromium was determined by atomic absorption spectrophotometer (Perkin Elmer). The results depicted that the efficiency of removal increased with increasing pH and bed height and decreased with increasing concentration. The removal efficiency with fly ash as an adsorbent was comparatively better than activatedcarbon. Thus, adsorbents can be used for chromium removal from tannery industry effluent.

Estimation of trace elements in sound and carious enamel of primary and permanent teeth by atomic absorption spectrophotometry: an in vitro study.

The influence of trace elements on the prevalence of caries is a complex subject. However, the demonstration of an inverse relationship between caries prevalence and fluoride (F) intake indicates the potential effect of trace elements on caries. AIMS AND OBJECTIVES: This in vitro study sought to estimate and compare the trace element concentrations in sound and carious enamel of primary and permanent teeth. MATERIALS AND METHODS: Forty sound and carious primary and permanent teeth, extracted from children and adolescents of Davangere city, were collected. The teeth were divided into four groups (of ten each) and enamel samples were prepared by mechanical grinding. The trace elements were estimated using atomic absorption spectrophotometer. RESULTS AND CONCLUSIONS: The results of our study showed the presence of 18 trace elements (F, Sr, K, Al, Si, Ni, B, Fe, Cu, Mn, Co, Cr, Zn, Mg, Se, Pb, Mo, and V) in the enamel of sound and carious primary and permanent teeth. The mean, standard deviation, and range (at 95% confidence level) were calculated for each element. The concentrations of F, Sr, and K were significantly ( P <0.05) higher in sound enamel of permanent teeth than in sound enamel of primary teeth. The concentrations of F, Sr, K, Al, and Fe were significantly ( P <0.05) higher in sound enamel of permanent teeth than in carious enamel of permanent teeth. The concentrations of F, K, and Si were significantly ( P <0.05) higher in sound enamel of primary teeth than in carious enamel of primary teeth.

Movement and bioaccumulation of chromium in an artificial freshwater ecosystem.

In the present study, a small fresh water aquatic ecosystem was created into a small test tank to evaluate the movement and bioaccumulation of Cr (VI) through water, sediment, a macrophyte Hydrilla, small fish guppy, and few key organs of magur, Clarias batrachus. The Cr (VI) intoxication was imposed of as a single dose of 30 mg/l concentration for a wide range of exposure durations like 1, 7, 14 and 21 days. After 1 day of exposure the total Cr (VI) load was very high in the water and sediment samples (5.187 microg/ml and 23.332 microg/g respectively) which were decreased with increasing exposure durations over their respective controls. In samples of macrophyte, Cr (VI) concentration showed a gradual increasing trend from 6.1797 microg/g in control to 21.1903 microg/g in 1 day exposure and reached up to 24.635 microg/g after 21 days exposure. In guppy, the Cr (VI) bioaccumulation showed an increasing trend but the rate was not statistically significant. However, in magur, the Cr (VI) uptake showed a significant gradual and increasing trend with increasing exposure durations in liver, brain, intestine and muscular tissues than gill and kidney over their respective controls. The movement of the Cr (VI) was found to be from sediment to water during pre-treatment phase, after intoxication, from water to macrophyte and to other phytoplankton and zooplankton. It then accumulated in the primary consumer guppy and finally moved to the secondary consumer the magur following the food web. The results reveal that the rate of movement and bioaccumulation of Cr (VI) varied from organism to organism and in C. batrachus, from tissue to tissue.