Sample records for diphenylcarbazides

  1. Assessment of chromium(VI) release from 848 jewellery items by use of a diphenylcarbazide spot test

    Bregnbak, David; Johansen, Jeanne D.; Hamann, Dathan;


    We recently evaluated and validated a diphenylcarbazide(DPC)-based screening spot test that can detect the release of chromium(VI) ions (≥0.5 ppm) from various metallic items and leather goods (1). We then screened a selection of metal screws, leather shoes, and gloves, as well as 50 earrings...

  2. Chromium(VI) release from leather and metals can be detected with a diphenylcarbazide spot test

    Bregnbak, David; Johansen, Jeanne D.; Jellesen, Morten Stendahl


    Along with chromium, nickel and cobalt are the clinically most important metal allergens. However, unlike for nickel and cobalt, there is no validated colorimetric spot test that detects chromium. Such a test could help both clinicians and their patients with chromium dermatitis to identify culprit...... exposures. To evaluate the use of diphenylcarbazide (DPC) as a spot test reagent for the identification of chromium(VI) release. A colorimetric chromium(VI) spot test based on DPC was prepared and used on different items from small market surveys. The DPC spot test was able to identify chromium(VI) release...... at 0.5 ppm without interference from other pure metals, alloys, or leather. A market survey using the test showed no chromium(VI) release from work tools (0/100). However, chromium(VI) release from metal screws (7/60), one earring (1/50), leather shoes (4/100) and leather gloves (6/11) was observed. We...

  3. Indirect spectrophotometric method for determination of captopril using Cr(VI and diphenylcarbazide

    Zenovia Moldovan


    Full Text Available A spectrophotometric method for the indirect determination of captopril (CP in pharmaceutical formulations is proposed. The proposed procedure is based on the oxidation of captopril by potassium dichromate and the determination excess oxidant on the basis of its reaction with diphenylcarbazide (DPC. Under the optimum conditions, a good linear relationship (r = 0.9997 was obtained in the range of 0.08-3.5 µg mL-1. The assay limits of detection and quantitation were 0.024 and 0.08 µg mL-1, respectively. The results obtained for captopril determination in pharmaceuticals using the proposed method and those obtained with the US Pharmacopoeia method were in good agreement at the 95% confidence level.

  4. Preparation of Diphenylcarbazide-Directed CdSe Quantum Dots and Selective Determination for Cr(Ⅵ)

    SHI Yan; SUN Ken


    CdSe quantum dots (QDs) were synthesized using diphenylcarbazide (DL) to sequester QDs precursors (Cd2+)in situ. Fluorescence (FL) analysis showed the successive synthesis of QDs could be realized by capping with DL and the binding between DL and Cd2+. The average QDs particle size was about 5-20 nm by high-resolution transmission electron microscopy (HRTEM). Fourier transform infrared (FT-IR) spectra showed that CdSe QDs could be chemically bonded with DL. The formation of QDs-DL-Cr(Ⅵ) could lower the lfuorescence intensity of QDs. In a certain concentration range, the lfuorescence intensity and Cr(Ⅵ) concentration presented a linear relationship. As a result, this phenomenon could be used to determine the Cr(Ⅵ) concentration in the range of 0-24 ×10−6 mol· L−1.

  5. Solid phase extraction of chromium(VI) from aqueous solutions by adsorption of its diphenylcarbazide complex on an Amberlite XAD-4 resin column.

    Rajesh, N; Jalan, Rohit Kumar; Hotwany, Pinky


    A method has been developed for the solid phase extraction of chromium(VI) based on the adsorption of its diphenylcarbazide complex on an Amberlite XAD-4 resin column. The influence of acidity, stability of the column, sample volume, flow rate and interfering ions were studied in detail. The adsorbed complex could be eluted using acetone-sulfuric acid mixture and the concentration of chromium was determined using visible spectrophotometry. A detection limit of 6 microg L(-1) could be achieved. A preconcentration factor of 27 could be obtained for 400 mL sample volume. The validity of the method was checked in spiked water samples and electroplating wastewater.

  6. Influence of pH Value on the Determination of Hexavalent Chromium by Diphenylcarbazide Spectrophotometry%pH值对二苯碳酰二肼分光光度法测定六价铬的影响

    王海云; 李敏锐; 廖涛; 谭飞帆; 邓杰


    Based on the 1,5 -diphenylcarbazide spectrophotometry, we researched on the influence of pH value on the determination of hexavalent chromium. By adding different amounts of acid into two water samples with different volumes and concentrations, we measured the absorbances of the solutions so as to determine the hexavalent chromium. Through analysis by EXCEL on the measured data, we found that the absorbance reduced with the decrease of pH value. In the presence of high acidity, which means small pH value, the measured hexavalent chromium was smaller than the original value before adding acid. Therefore, the variation of pH value had an impact on the measurement of hexavalent chromium. Moreover, we employed the gray system model GM( 1,1) to process the experimental data, and derived a linear equation for the absorbance under different acidities. Through t test and F test, no significant difference was found between calculated absorbance and measured absorbance. This research is helpful to quantitatively looking into the influence of pH value on hexavalent chromium determination.%为获得不同pH值对测定六价铬(Cr(Ⅵ))的影响,以标准分析方法二苯碳酰二肼(C13H14N4O)分光光度法为基础,选用2种体积浓度的水样,分别加入不同的酸量,测定吸光度.经EXCEL软件对实测数据分析,得出加酸量与吸光度具有紧密的相关性,发现吸光度随着溶液pH值的减小而减小,酸度偏大,测定的实际结果比真实值小,pH值的不同对Cr(Ⅵ)测定结果具有影响.采用灰色系统模型GM(1,1)对实验数据进行处理,推导出不同酸度下的吸光度直线方程式.经t检验和F检验证明,计算出的吸光度值与测定值不存在显著性差异,可帮助定量掌握不同酸度条件下对测定Cr(Ⅵ)产生影响具有一定的作用.

  7. 减小水样浊度对废水中六价铬测定结果影响的方法探讨%Effect Elimination of Turbidity on Diphenylcarbazide Spectrophotometric Measurement of Cr( Ⅵ ) in Waste Waters



    Triplex-wavelength spectrophotometric methods using diphenylcarbazide as a chromogenic reagent was established to eliminate the interference of turbidity for determining Cr( VI) in waste water. However, this method could not be used to eliminate the effect of other factors on Cr( VI) except for turbidity. In the triplex-wavelength spectrophotometric method, the measuring wavelength was 540 nm, and the reference wavelengths were 460 run and 660 nm. The triplex-wavelength spectrophotometric method had a good correlation coefficient ( r = 0. 9998 ) and precision (RSD 1.44% , for seven 8. 0 μg/L standard samples). The detection limit (LD =3. 143s) was 0. 3 μg/L. The average value of recoveries in waste water samples were in the range of 84. 8% - 93. 8% using an internal standard. Compared with the single-wavelength spectrophotometric method, the triplex-wavelength spectrophotometric method had better precision and accuracy. Furthermore, the triplex-wavelength spectrophotometric method had better precision and less workload than the turbidity compensation spectrophotometric method. This method is suitable for the determination of Cr( VI) in low turbidity waste water when the absorbency is lower than 0. 1000 at 540 nm. High turbidity waste water needs to be diluted before spectrophotometric measurements can be made.%建立了二苯碳酰二肼分光光度法测定废水中Cr(Ⅵ)的三波长法,减小了水样浊度的影响,但不能减小除浊度之外的其他干扰对Cr(Ⅵ)测定结果的影响.三波长法的测定波长为540 nm,460 nm和660 nm为参比波长,方法检出限为0.3 μg/L(3.143s),拟合方程的线性关系为0.9998,8.0 μg/L标准点水样测定结果的相对标准偏差( RSD,n=7)为1.44%,实际样品加标回收率均值为84.8%~93.8%.与单波长法相比,三波长法提高了二苯碳酰二肼分光光度法测定水中Cr(Ⅵ)的精密度和准确度,与浊度补偿法相比具有较好的精密度,可减轻分析人员的工作量.

  8. Estudo comparativo da eficiência da difenilcarbazida e do óleo de coco saponificado microemulsionados na inibição da corrosão de aço carbono Comparative effectiveness microemulsions of diphenylcarbazide and saponified coconut oil in the carbon steel corrosion inhibition process

    Cátia G. F. T. Rossi


    Full Text Available The effectiveness of microemulsions (ME of saponified coconut oil (OCS-ME and diphenylcarbazide (DC-ME on a carbon steel corrosion inhibition process was evaluated using an electrochemical method of polarization resistance. The ME was prepared with OCS, butanol, kerosene and saline solutions. OCS-ME and DC-ME showed highest inhibitions effects (77% and 92%, respectively at lower concentrations (0.5% and 0.48 - 0.50%, respectively. The surfactant OCS (in H2O showed lower efficiency (63% at 0.20 - 0.25% concentration. The greatest inhibitory effect of DC-ME could be correlated with the chemical structure and the rich O/W ME system, which are very important for adsorption phenomena in interfacial ME systems.

  9. Determinação de rotina do crômio em fezes, como marcador biológico, pelo método espectrofotométrico ajustado da 1,5-difenilcarbazida The spectrophotometric method on the routine of 1,5-diphenylcarbazide was adjusted on chromium determination in feces, after its utilization as a biological marker as chromium (III oxide

    Hermann Bremer Neto


    Full Text Available O objetivo deste estudo foi ajustar o método espectrofotométrico da 1,5-difenilcarbazida à determinação do crômio em fezes, como marcador biológico, adequando-o à rotina laboratorial. Fatores que poderiam exercer interferência na transformação do crômio (III à crômio (VI foram testados, como a recuperação do metal, quantidade de amostra, quantidade e ordem de emprego dos ácidos oxidantes da digestão úmida, temperatura e tempo de digestão e perda por volatilização do crômio como cloreto de cromila, porém não se determinou estatisticamente interferência destes fatores. No método ajustado, a amostra é digerida pela clássica mistura ácida nítrica/perclórica, levando a oxidação do crômio (III a crômio (VI, e alíquota do extrato diluído é usado para reação com 1,5-difenilcarbazida; as absorbâncias são medidas a 550nm, utilizando-se de cubetas de um centímetro de caminho óptico, contra prova em branco conduzida simultaneamente. Dicromato de potássio foi empregado como substância de referência para obtenção da curva padrão na faixa de 0,25 - 2,5mg.mL-1 de Cr2O3 (1mg Cr2O3 º 1,9355mg K2Cr2O7.This work aims at adjusting the spectrophotometric method of 1,5-diphenylcarbazide for the determination of chromium in feces, as a biological marker. Factors that could interfere with the transformation of chromium (III into chromium (VI were tested, as the metal recovery, the sample amount, the amount and the order of use of the oxidant acids of the wet digestion, digestion temperature and digestion time, loss of chromium by volatilization as chromyl chlorid. However the interference of these factors were not statistically determined. In the adjusted method, the sample is classically digested by nitric/perchloric acid mixture leading to the oxidation of chromium (III to chromium (VI, and an aliquot of the diluted extract is used for reaction with 1,5-diphenylcarbazide; absorbance was measured at 550nm, using 1cm

  10. Spectrophotometric determination of chromium with diphenylcarbazide in the presence of vanadium, molybdenum, and iron after separation by solid-phase extraction

    Llobat-Estelles, M.; Mauri-Aucejo, A.R.; Lopez-Catalan, M.D. [Dept. de Quimica Analitica, Univ. de Valencia Estudi General, Burjassot (Spain)


    A method has been developed for the determination of chromium in presence of V(V), Mo(VI), and Fe(III). The effects of interferences were evaluated by using the apparent content curves method, and their separation was performed by solid-phase extraction with an anionic exchanger. The sample-treatment conditions and the influence of the sample conductivity were studied. Tolerance limits were established, and the proposed procedure was used to determine chromium in certified samples and for speciation of chromium in waste water. Our results were always in agreement with the theoretical content. (orig.)

  11. Thermodynamic Properties of Chromium Adsorption by Sediments ...



    Jun 19, 2013 ... diphenylcarbazide as a colour developing reagent has been used to ... applied to model adsorption on natural materials. Three typical ... showed that several negatively charged dyes were investigated for ... The result showed that the dye was probably ... de-ionised water were used for the preparation of.

  12. On-line Speciation of Cr(III) and Cr(VI) by Flow Injection Analysis With Spectrophotometric Detection and Chemometrics

    Diacu, Elena; Andersen, Jens Enevold Thaulov


    A flow injection system has been developed, for on-line speciation. of Cr(III) and Cr(VI) by the Diphenylcarbazide (DPC) method with H2O2 oxidation followed by spectrophotometric detection at the 550 nm wavelength. The data thus obtained were subjected to a chemometric analysis (PLS), which showe...

  13. Myrsinoic A acid and its derivative: in vitro inhibitors of photosynthesis; Acido myrsinoico A e derivado: inibidores da fotossintese in vitro

    Burger, Marcela Carmen de M.; Oliveira, Gracielle S. de; Menezes, Antonio Carlos S. [Universidade Estadual de Goias, Anapolis, GO (Brazil). Unidade Universitaria de Ciencias Exatas e Tecnologicas; Vieira, Paulo Cezar; Silva, Maria Fatima das G.F. da [Universidade Federal de Sao Carlos (UFSCar), SP (Brazil). Dept. de Quimica; Veiga, Thiago A.M., E-mail: [Universidade Federal de Sao Paulo (UNIFESP), SP (Brazil). Inst. de Ciencias Ambientais, Quimicas e Farmaceuticas. Dept. de Ciencias Exatas e da Terra


    Myrsinoic A acid, isolated from Myrsine cuneifolia and its hydrogenated derivative had their effect on photosynthesis tested. The compounds inhibited the electron flow (basal, phosphorylating and uncoupled) from water to methyl viologen; therefore, they act as Hill reaction inhibitors in spinach thylakoids. They inhibited partial reactions of PSII electron flow from water to 2,5-dichloro-1,4-benzoquinone, from water to sodium silicomolybdate, and partially electron flow from diphenylcarbazide to 2,6-dichloroindophenol. Their inhibition sites were at the donor and acceptor sides of PSII, between P{sub 680} and Q{sub A}. Chlorophyll {alpha} fluorescence measurements confirmed the behavior of the compounds (pool of quinones). (author)

  14. Effects of 2-alkylthio-6-aminobenzothiazoles and their 6-N-substituted derivatives on photosynthesis inhibition in Chlorella vulgaris and spinach chloroplasts.

    Král'ová, K; Sersen, F; Sidóová, E


    2-Alkylthio-6-aminobenzothiazoles and their 6-N-substituted derivatives 3-(2-alkylthio-6-benzothiazolylaminomethyl)-2-benzothiazolineth iones and 3-(2-alkylthio-6-benzothiazolylaminomethyl)-6-bromo-2-benzothia zolinones inhibit photosynthetic processes in spinach chloroplasts and the chlorophyll production in Chlorella vulgaris. The inhibitory activity depends on the alkyl chain length of the thioalkyl substituent. The site of action of the effectors studied is on the donor side of photosystem 2 before the site of action of diphenylcarbazide. The highest antialgal effects were exhibited by compounds containing bromine.

  15. Spermine and spermidine inhibition of photosystem II: Disassembly of the oxygen evolving complex and consequent perturbation in electron donation from TyrZ to P680+ and the quinone acceptors QA- to QB.

    Beauchemin, Rémy; Gauthier, Alain; Harnois, Johanne; Boisvert, Steve; Govindachary, Sridharan; Carpentier, Robert


    Polyamines are implicated in plant growth and stress response. However, the polyamines spermine and spermidine were shown to elicit strong inhibitory effects in photosystem II (PSII) submembrane fractions. We have studied the mechanism of this inhibitory action in detail. The inhibition of electron transport in PSII submembrane fractions treated with millimolar concentrations of spermine or spermidine led to the decline of plastoquinone reduction, which was reversed by the artificial electron donor diphenylcarbazide. The above inhibition was due to the loss of the extrinsic polypeptides associated with the oxygen evolving complex. Thermoluminescence measurements revealed that charge recombination between the quinone acceptors of PSII, QA and QB, and the S2 state of the Mn-cluster was abolished. Also, the dark decay of chlorophyll fluorescence after a single turn-over white flash was greatly retarded indicating a slower rate of QA- reoxidation.

  16. Inhibitory effect of some carbazides on corrosion of aluminium in hydrochloric acid and sodium hydroxide solutions

    Fouda, A.S. [El-Mansoura Univ. (Egypt). Dept. of Chemistry; Madkour, L.H. [Tanta Univ. (Egypt). Dept. of Chemistry; Elshafei, A.A. [El-Mansoura Univ. (Egypt). Dept. of Chemistry; Elasklany, A.H. [El-Mansoura Univ. (Egypt). Dept. of Chemistry


    The dissolution of aluminium in hydrochloric acid and sodium hydroxide solutions in the presence of semicarbazide, thiosemicarbazide and sym.diphenylcarbazide as corrosion inhibitors has been studied using thermometric, weight-loss and polarization methods. The three methods gave consistent results. The higher inhibition efficiency of these compounds in acidic than in alkaline madia may be due to the less negative potential of aluminium in hydrochloric acid solution, favouring adsorption of the additive. The adsorption of these compounds were found to obey Frumkin adsorption isotherm. Cathodic polarization measurements showed that these compounds are cathodic inhibitors and their adsorption in the double layer does not change the mechanism of the hydrogen evolution reaction. The results are analysed in terms of both molecular and cationic adsorption. (orig.)

  17. Light-triggered selective nitration of PsbO1 in isolated Arabidopsis thylakoid membranes is inhibited by photosynthetic electron transport inhibitors.

    Takahashi, Misa; Shigeto, Jun; Sakamoto, Atsushi; Morikawa, Hiromichi


    PsbO1 is exclusively nitrated when isolated thylakoid membranes are incubated in a buffer bubbled with nitrogen dioxide (NO2) containing NO2 and nitrite. NO2 is the primary intermediate for this selective nitration. Isolated thylakoid membranes were incubated in NO2-bubbled buffer at 25°C in the light or dark. Protein analysis confirmed the selective nitration of PsbO1. Illumination was found to be essential in PsbO1 nitration. A nitration mechanism whereby nitratable tyrosine residues of PsbO1 are, prior to nitration, selectively photo-oxidized by photosynthetic electron transport to tyrosyl radicals to combine with NO2 to form 3-nitrotyrosine was hypothesized. We tested the electron transport inhibitors 3-(3,4-dichlorophenyl)-1,1- dimethylurea, sodium azide, and 1,5-diphenylcarbazide and found distinct inhibition of nitration of PsbO1. We also propose a possible nitration mechanism.

  18. Hexavalent Chromium Removal by Litchi chinensis Sonn Peel

    Ismael Acosta-Rodriguez


    Full Text Available Problem statement: We studied the Chromium (VI removal capacity in aqueous solution by the litchi peel. Approach: We use the diphenylcarbazide method to evaluate the metal concentration. Results: The highest biosorption of the metal (50 mg L-1 occurs within 6 min, at pH of 1 and 28°C. According to temperature, the highest removal was observed at 40 and 50°C, in 45 min, when the metal (1 g L-1 was completely adsorbed. At the analyzed concentrations of Cr (VI, litchi peel, showed excellent removal capacity, besides it removes efficiently the metal in situ (100% removal, 5 days of incubation, 5 and 10 g of biomass. After 1 h of incubation the studied biomass reduces 1.0 g of Cr (VI with the simultaneous production of Cr (III. Conclusion: The shell can be used to eliminate it from industrial wastewater."

  19. Evaluation of herbicidal potential of depsides from Cladosporium uredinicola, an endophytic fungus found in Guava fruit

    Medeiros, Livia S. de; Sampaio, Olivia M.; Silva, Maria Fatima das G.F. da; Rodrigues Filho, Edson [Departamento de Quimica, Universidade Federal de Sao Carlos, SP (Brazil); Veiga, Thiago Andre M., E-mail: [Instituto de Ciencias Ambientais, Quimicas e Farmaceuticas, Universidade Federal de Sao Paulo, Diadema, SP (Brazil)


    Two natural products produced by Cladosporium uredinicola, an endophytic fungus isolated from guava fruit, were evaluated for their effects on photosynthesis. Both of them inhibited electron flow (basal, phosphorylating, and uncoupled) from water to methylviologen (MV), acting as Hill reaction inhibitors in freshly lysed spinach thylakoids. These polyketides, belonging to depsides class, inhibited partial reactions of photosystem II (PS II) electron flow from water to 2,5-dichloro-1,4-benzoquinone (DCBQ), from water to sodium silicomolybdate (SiMo Na{sup +}), and partially inhibited electron flow from 1,5-diphenylcarbazide (DPC) to 2,6-dichloroindophenol (DCPIP). These results established that the depsides sites of inhibition are located on the donor and acceptor sides of PS II, between P680 and QA . Chlorophyll a fluorescence measurements corroborated this mechanism of action. None of the tested compounds inhibited photosystem I (PS I) electron transport. (author)

  20. Electron transport, Photosystem-2 reaction centers and chlorophyll-protein complexes of thylakoids of drought resistant and sensitive Lupin piants.

    Meyer, S; de Kouchkovsky, Y


    Two genotypes ofLupinus albus L., resistant and susceptible to drought, were subjected to water deficiency for up to two weeks. Such treatment progressively lowered the leaf water content from about 85% to about 60% (water potential from -0.8 to -4.3 MPa). Light-saturation curves of the uncoupled electron transport were analyzed according to a simple kinetic model of separated or connected reversible photoreactions. It gives an extrapolated maximum rate (Vmax) and the efficiency for capturing light (Im, which is the light intensity at Vmax/2). For Photosystem 2, Vmax and, less markedly, Im, declined with increasing severity of drought treatment; the artificial donor, diphenylcarbazide, could not restore the activity. One cause of this Photosystem 2 inhibition could be the loss of active Photosystem 2 centers. Indeed, their concentration relative to chlorophyll, estimated by flash-induced reduction of dimethylquinone, was halved by a medium stress. To the extent that it was still not restored by diphenylcarbazide, the site of Photosystem 2 inactivation must have been close to the photochemical trap, after water oxidation and before or at plastoquinone pool. By relating electron transport rate to active centers instead of chlorophyll, no inhibition by drought was detected. Therefore, water stress inactivates specifically Photosystem 2, without impairing a downhill thermal step of electron transport. On the other hand, the decrease of Im suggests that antennae connected to inactive centers may transfer their excitation energy to active neighbors, which implies that antenna network remains essentially intact. Gel electrophoresis confirmed that the apoproteins of the pigment complexes were well conserved. In conclusion, the inactivation of Photosystem 2 may not be a physical loss of its centers and core antennae but probably reflects protein alterations or conformational changes. These may result from the massive decrease of lipids induced by drought (Meyer et al. 1992

  1. Chromium(III, VI) speciation analysis with preconcentration on a maleic acid-functionalized XAD sorbent

    Yalcin, Sibel; Apak, Resat


    Chromium may exist in environmental waters as Cr(III) and Cr(IV), the latter being the toxic and carcinogenic form. Since atomic absorption spectrometry (AAS) and inductively coupled plasma atomic emission spectrometry can only yield information on total Cr concentration, a polymer resin bearing O,O-donor chelating groups such as the maleic acid-functionalized XAD-(CO)CH-CH-COOH resin was synthesized to selectively retain Cr(III) at pH 4.0-5.5. The dynamic breakthrough capacity of the resin for Cr(III) at pH 5.0 was 7.52 mg g{sup -1}, and the preconcentration factor extended to 250-300. Chromium(III) in the presence of 250-fold Cr(VI)--which was not retained--could be effectively preconcentrated on the NH{sub 4}{sup +}-form of the resin and determined by AAS or diphenylcarbazide (DPC) spectrophotometry. When Cr(VI) was reduced to Cr(III) with Na{sub 2}SO{sub 3} solution brought to pH 1 by the addition of 1 M H{sub 2}SO{sub 4}, and preconcentrated on the resin, total Cr could be determined. The developed method was validated with a blended coal sample CRM-1632. Since the adsorption behavior as a function of pH of possible interferent metal ions, e.g. Ni(II), Co(II), Cu(II), Cd(II), Zn(II), Pb(II) and Fe(III), was similar to that of Cr(III), selective elution of Cr(III) from the resin was realized using a mixture of 1 wt.% H{sub 2}O{sub 2}+1 M NH{sub 3}. The eluate containing Cr as chromate could be directly analyzed by diphenyl carbazide spectrophotometry without any adverse effect from the common interferents of this method, i.e. Fe(III), Cu(II) Hg(II), VO{sub 3}{sup -}, MoO{sub 4}{sup 2-} and WO{sub 4}{sup 2-}. Various synthetic waste solutions typical of electroplating bath effluents containing Cr, Cu, Ni, Zn, Na, Ca, cyanide (and chemical oxidation demand (COD), achieved by glucose addition) were subjected to pretreatment procedures such as hypochlorite oxidation (of cyanide) and catalytic oxidation (of COD) with peroxodisulfate. Chromium determination gave

  2. Chemical, mass spectrometric, spectrochemical, nuclear, and radiochemical analysis of nuclear-grade uranyl nitrate solutions


    The standard covers analytical procedures to determine compliance of nuclear-grade uranyl nitrate solution to specifications. The following methods are described in detail: uranium by ferrous sulfate reduction-potassium dichromate titrimetry and by ignition gravimetry; specific gravity by pycnometry; free acid by oxalate complexation; thorium by the Arsenazo(III) (photometric) method; chromium by the diphenylcarbazide (photometric) method; molybdenum by the thiocyanate (photometric) method; halogens separation by steam distillation; fluorine by specific ion electrode; halogen distillate analysis: chloride, bromide and iodide by amperometric microtitrimetry; bromine by the fluorescein (photometric) method; sulfate sulfur by (photometric) turbidimetry; phosphorus by the molybdenum blue (photometric) method; silicon by the molybdenum blue (photometric) method; carbon by persulfate oxidation-acid titrimetry; nonvolatile impurities by spectrography; volatile impurities by rotating-disk spark spectrography; boron by emission spectrography; impurity elements by spark source mass spectrography; isotopic composition by multiple filament surface-ionization mass spectrometry; uranium-232 by alpha spectrometry; total alpha activity by direct alpha counting; fission product activity by beta and gamma counting; entrained organic matter by infrared spectrophotometry. (JMT)

  3. Groundwater contaminated with hexavalent chromium [Cr (VI]: a health survey and clinical examination of community inhabitants (Kanpur, India.

    Priti Sharma

    Full Text Available BACKGROUND: We assessed the health effects of hexavalent chromium groundwater contamination (from tanneries and chrome sulfate manufacturing in Kanpur, India. METHODS: The health status of residents living in areas with high Cr (VI groundwater contamination (N = 186 were compared to residents with similar social and demographic features living in communities having no elevated Cr (VI levels (N = 230. Subjects were recruited at health camps in both the areas. Health status was evaluated with health questionnaires, spirometry and blood hematology measures. Cr (VI was measured in groundwater samples by diphenylcarbazide reagent method. RESULTS: Residents from communities with known Cr (VI contamination had more self-reports of digestive and dermatological disorders and hematological abnormalities. GI distress was reported in 39.2% vs. 17.2% males (AOR = 3.1 and 39.3% vs. 21% females (AOR = 2.44; skin abnormalities in 24.5% vs. 9.2% males (AOR = 3.48 and 25% vs. 4.9% females (AOR = 6.57. Residents from affected communities had greater RBCs (among 30.7% males and 46.1% females, lower MCVs (among 62.8% males and less platelets (among 68% males and 72% females than matched controls. There were no differences in leucocytes count and spirometry parameters. CONCLUSIONS: Living in communities with Cr (VI groundwater is associated with gastrointestinal and dermatological complaints and abnormal hematological function. Limitations of this study include small sample size and the lack of long term follow-up.

  4. Selective sampling and measurement of Cr (VI) in water with polyquaternary ammonium salt as a binding agent in diffusive gradients in thin-films technique.

    Chen, Hong; Zhang, Yang-Yang; Zhong, Ke-Li; Guo, Lian-Wen; Gu, Jia-Li; Bo, Le; Zhang, Meng-Han; Li, Jian-Rong


    A diffusive gradients in thin films (DGT) device with polyquaternary ammonium salt (PQAS) as a novel binding agent (PQAS DGT) combined with graphite furnace atomic absorption spectrometry (GFAAS) was developed for the selective sampling and measurement of Cr (VI) in water. The performance of PQAS DGT was independent of pH 3-12 and ionic strength from 1 × 10(-3) to 1 molL(-1). DGT validation experiments showed that Cr (VI) was measured accurately as well as selectively by PQAS DGT, whereas Cr (III) was not determined quantitatively. Compared with diphenylcarbazide spectrophotometric method (DPC), the measurement of Cr (VI) with PQAS DGT was agreement with that of DPC method in the industrial wastewater. PQAS-DGT device had been successfully deployed in local freshwater. The concentrations of Cr (VI) determined by PQAS DGT coupled with GFAAS in Nuer River, Ling River and North Lake were 0.73 ± 0.09 μg L(-1), 0.50 ± 0.07 μg L(-1) and 0.61 ± 0.07 μg L(-1), respectively. The results indicate that PQAS DGT device can be used for the selective sampling and measurement Cr (VI) in water and its detection limit is lower than that of DPC method. Copyright © 2014 Elsevier B.V. All rights reserved.

  5. Adsorption of Chromium(VI from Aqueous Solutions by Coffee Polyphenol-Formaldehyde/Acetaldehyde Resins

    Khudbudin Mulani


    Full Text Available Removal of chromium(VI from wastewater is essential as it is toxic. Thus, removal of chromium(VI was performed using coffee polyphenol-formaldehyde/acetaldehyde resins as adsorbents. Adsorbent resins were prepared by condensation of decaffeinated coffee powder with formaldehyde/acetaldehyde and used for the removal of Cr(VI ions from aqueous solutions. A simple and sensitive solid phase extraction procedure was applied for the determination of chromium at trace levels by spectroscopic method using 1,5-diphenylcarbazide reagent. The adsorption of Cr(VI on the coffee polyphenol-formaldehyde/acetaldehyde resins was monitored by FTIR and EDX analysis. The metal adsorption parameters such as contact time, pH, Cr(VI ion concentration, and adsorbent dose were investigated. For Cr(VI, the maximum adsorption capacity of coffee polyphenol-formaldehyde resins was 98% at pH 2. The experimental results showed that Cr(VI bound strongly with coffee polyphenol-formaldehyde/acetaldehyde resins and utilization of resins could be improved greatly by reuse.

  6. Mexican propolis flavonoids affect photosynthesis and seedling growth.

    King-Díaz, Beatriz; Granados-Pineda, Jessica; Bah, Mustapha; Rivero-Cruz, J Fausto; Lotina-Hennsen, Blas


    As a continuous effort to find new natural products with potential herbicide activity, flavonoids acacetin (1), chrysin (2) and 4',7-dimethylnarangenin (3) were isolated from a propolis sample collected in the rural area of Mexico City and their effects on the photosynthesis light reactions and on the growth of Lolium perenne, Echinochloa crus-galli and Physalis ixocarpa seedlings were investigated. Acacetin (1) acted as an uncoupler by enhancing the electron transport under basal and phosphorylating conditions and the Mg(2+)-ATPase. Chrysin (2) at low concentrations behaved as an uncoupler and at concentrations up to 100 μM its behavior was as a Hill reaction inhibitor. Finally, 4',7-dimethylnarangenin (3) in a concentration-dependent manner behaved as a Hill reaction inhibitor. Flavonoids 2 and 3 inhibited the uncoupled photosystem II reaction measured from water to 2,5-dichloro-1,4-benzoquinone (DCBQ), and they did not inhibit the uncoupled partial reactions measured from water to sodium silicomolybdate (SiMo) and from diphenylcarbazide (DPC) to diclorophenol indophenol (DCPIP). These results indicated that chrysin and 4',7-dimethylnarangenin inhibited the acceptor side of PS II. The results were corroborated with fluorescence of chlorophyll a measurements. Flavonoids also showed activity on the growth of seedlings of Lolium perenne and Echinochloa crus-galli. Copyright © 2015 Elsevier B.V. All rights reserved.

  7. Determination of the bioaccessibility of chromium in Glasgow soil and the implications for human health risk assessment.

    Broadway, Andrew; Cave, Mark R; Wragg, Joanna; Fordyce, Fiona M; Bewley, Richard J F; Graham, Margaret C; Ngwenya, Bryne T; Farmer, John G


    The Unified Bioaccessibility Method (UBM), which simulates the fluids of the human gastrointestinal tract, was used to assess the oral bioaccessibility of Cr in 27 Glasgow soils. These included several contaminated with Cr(VI), the most toxic form of Cr, from the past disposal of chromite ore processing residue (COPR). The extraction was employed in conjunction with the subsequent determination of the bioaccessible Cr by ICP-OES and Cr(VI) by the diphenylcarbazide complexation colorimetric procedure. In addition, Cr(III)-containing species were determined by (i) HPLC-ICP-MS and (ii) ICP-OES analysis of gel electrophoretically separated components of colloidal and dissolved fractions from centrifugal ultrafiltration of extracts. Similar analytical procedures were applied to the determination of Cr and its species in extracts of the complexes. Insertion of oral bioaccessible fraction data into the SNIFFER human health risk assessment model identified site-specific assessment criteria (for residential land without plant uptake) that were exceeded by the soil total Cr (3680 mg kg(-1)) and Cr(VI) (1485 mg kg(-1)) concentration at only the most COPR-Cr(VI)-contaminated location. However, the presence of measurable Cr(VI) in the <10 μm fraction of the two most highly Cr(VI)-contaminated soils demonstrated that inhalation of Cr(VI)-containing dust remains the most potentially harmful exposure route.

  8. Correlation between bulk- and surface chemistry of Cr-tanned leather and the release of Cr(III) and Cr(VI).

    Hedberg, Yolanda S; Lidén, Carola; Odnevall Wallinder, Inger


    About 1-3% of the adult general population in Europe is allergic to chromium (Cr). The assessment of the potential release of Cr(III) and Cr(VI) from leather is hence important from a human health and environmental risk perspective. The Cr(VI) content in leather was recently restricted in the European Union. The aim of this study was to assess possible correlations between the bulk and surface chemistry of leather, released Cr(III) and Cr(VI), and capacities of co-released leather specific species to reduce and complex released Cr. Four differently tanned leathers were characterized by scanning electron microscopy with energy dispersive spectroscopy, X-ray photoelectron spectroscopy, attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy, and the diphenylcarbazide colorimetric method. Their characteristics were compared with results on Cr(III) and Cr(VI) release into artificial sweat (ASW, pHleather-specific species were shown to reduce Cr(VI), both in ASW and in PB. Their reduction capacities correlated with findings of the surface content of Cr and of released Cr. Leather samples without this capacity, and with less aromatic surface groups visible by ATR-FTIR, revealed Cr(VI) both at the surface and in solution (PB).

  9. Environmental impacts of Sheba tannery (Ethiopia effluents on the surrounding water bodies

    Abraha Gebrekidan


    Full Text Available The levels of hexavalent chromium from direct and treated Sheba tannery effluents, downstream river and spring water samples and upstream river water samples were determined spectrophotometrically by the s-diphenylcarbazide method at 540 nm. Temporal and representative samples were collected from the untreated tannery effluent (S1, sedimentation pond (S2, chromium oxidation pond (S3, downstream river (S4, downstream spring (S5 and 5 kms upstream river (S6. The mean levels of hexavalent chromium in S1, S2, S3, S4, S5 and S6 were 10.54, 9.15, 7.82, 0.58, 0.54 and 0.015 mg/L, respectively. The levels of hexavalent chromium in the downstream river and spring water samples exceed the World Health Organization (WHO permissible limit of total chromium in drinking waters (0.05 mg/L as opposed to the levels in the upstream waters. The increased concentrations of Cr(VI in the water samples indicate the possible environmental pollution of the downstream water bodies by the Sheba tannery effluents. In view of the toxicity and related environmental hazards, the levels of hexavalent chromium from the Sheba tannery effluents must be reduced to a permissible limit before discharging into the down stream waters being used for domestic purposes by the nearby communities.

  10. Selective and sensitive speciation analysis of Cr(VI) and Cr(III) in water samples by fiber optic-linear array detection spectrophotometry after ion pair based-surfactant assisted dispersive liquid-liquid microextraction.

    Yousefi, Seyedeh Mahboobeh; Shemirani, Farzaneh


    A simple ion pair based-surfactant assisted dispersive liquid-liquid microextraction (IP-SA-DLLME) was evaluated for extraction and preconcentration of Cr(VI) and Cr(III) in aqueous samples. In this method, which was used for the first time for chromium speciation analysis, sodium dodecyl sulfate (SDS) was used as both ion-pairing and disperser agent. Cr(VI) ions were converted into their cationic complex with 1,5-diphenylcarbazide (DPC) and then extracted into 1-octanol dispersed in aqueous solution. Cr(III) ion also can be determined by this procedure after oxidation to Cr(VI). After extraction and phase separation, upper organic phase was transferred to a micro cell of a fiber optic-linear array detection spectrophotometry (FO-LADS). The effects of various parameters on the extraction recovery were investigated. Under the optimized conditions and preconcentration of 10 mL of sample, the enrichment factor of 159 and the detection limit of 0.05 μgL(-1) were obtained. Validation of the method was performed by spiking-recovery method and comparison of results with those obtained by ET-AAS method.

  11. Cloud point extraction and diffuse reflectance-Fourier transform infrared spectroscopic determination of chromium(VI): A probe to adulteration in food stuffs.

    Tiwari, Swapnil; Deb, Manas Kanti; Sen, Bhupendra K


    A new cloud point extraction (CPE) method for the determination of hexavalent chromium i.e. Cr(VI) in food samples is established with subsequent diffuse reflectance-Fourier transform infrared (DRS-FTIR) analysis. The method demonstrates enrichment of Cr(VI) after its complexation with 1,5-diphenylcarbazide. The reddish-violet complex formed showed λmax at 540nm. Micellar phase separation at cloud point temperature of non-ionic surfactant, Triton X-100 occurred and complex was entrapped in surfactant and analyzed using DRS-FTIR. Under optimized conditions, the limit of detection (LOD) and quantification (LOQ) were 1.22 and 4.02μgmL(-1), respectively. Excellent linearity with correlation coefficient value of 0.94 was found for the concentration range of 1-100μgmL(-1). At 10μgmL(-1) the standard deviation for 7 replicate measurements was found to be 0.11μgmL(-1). The method was successfully applied to commercially marketed food stuffs, and good recoveries (81-112%) were obtained by spiking the real samples. Copyright © 2016 Elsevier Ltd. All rights reserved.

  12. Preconcentration and Determination of Copper(Ⅱ) Using Octadecyl Silica Membrane Disks Modified by 1,5-Diphenylcarhazide and Flame Atomic Absorption Spectrometry



    A simple and reproducible method for the rapid extraction and determination of trace amounts of copper(Ⅱ)ions using octadecyl-bonded silica membrane disks modified by 1,5-diphenylcarbazide (DPC) and atomic absorption spectrometry was presented, which was based on complex formation on the surface of the ENVI-18 DISKTM disks followed by stripping of the retained species by minimum amounts of appropriate organic solvents. The elution was efficient and quantitative. The effect of potential interfering ions, pH, ligand amount, stripping solvent, and sample flow rate were also investigated. Under the optimal experimental conditions, the break-through volume was found to be about 1000 mL providing a preconcentration factor of 400. The maximum capacity of the disks was found to be (255±5) μg for Cu2+, and the limit of detection of the proposed method was 5 ng per 1000 mL. The method was applied to the extraction and recovery of copper in different water samples.

  13. Reduction of chromate and carotene-synthesizing activity of selenite-resistant mutants of the yeast Xanthophyllomyces dendrorhous (Phaffia rhodozyma

    Grzàdka M.


    Full Text Available Aim. The yeast P. rhodozyma is a perspective microbial producer of carotenoid pigment astaxanthin with a high antioxidant power. The aim of the work was to study the ability of the selenite-resistant strains of this yeast to reduce chrome(VI compounds, as well as to analyze the relations between synthesis of carotenoids, resistance to selenite and chromate-reducing activity of P. rhodozyma. Methods. The yeast cells were grown at standard conditions for this species. The residual chromate content in cultural liquid was determined colorimetrically using diphenylcarbazide. The carotenoid content was determined after extraction of the pigments from the previously permeabilized cells by organic solvents. Results. The selected selenite-resistant mutants of the yeast P. rhodozyma revealed the different combinations of the phenotypes related with tolerance/sensitivity to chromate and selenite, as well as ability to reduce chromate. Conclusions. The obtained results give reasons for suggesting that pathways of detoxification of chromate and selenite by the yeast P. rhodozyma are different, although run through a common reductive type. The isolated mutant strains would be served as the useful models to study relations between homeostasis of Se and Cr oxyanions and biosynthesis of carotenes.

  14. Modified hydrothermal synthesis and characterization of reduced graphene oxide-silver selenide nanocomposites with enhanced reactive oxygen species generation

    Lei Zhu; Shu Ye; Asghar Ali; Kefayat Ulla; Kwang Youn Cho; Won-Chun Oh


    A visible‐light photocatalyst containing Ag2Se and reduced graphene oxide (RGO) was synthesized by a facile sonochemical‐assisted hydrothermal method. X‐ray diffraction, scanning electron mi‐croscopy with energy‐dispersive X‐ray analysis, and ultraviolet‐visible diffuse reflectance spectros‐copy results indicated that the RGO‐Ag2Se nanocomposite contained small crystalline Ag2Se nano‐particles dispersed over graphene nanosheets and absorbed visible light. The high crystallinity of the nanoparticles increased photocatalytic activity by facilitating charge transport. N2 adsorp‐tion‐desorption measurements revealed that the RGO‐Ag2Se nanocomposite contained numerous pores with an average diameter of 9 nm, which should allow reactant molecules to readily access the Ag2Se nanoparticles. The RGO‐Ag2Se nanocomposite exhibited higher photocatalytic activity than bulk Ag2Se nanoparticles to degrade organic pollutant rhodamine B and industrial dye Texbrite BA‐L under visible‐light irradiation (λ>420 nm). The generation of reactive oxygen spe‐cies in RGO‐Ag2Se was evaluated through its ability to oxidize 1,5‐diphenylcarbazide to 1,5‐diphenylcarbazone. The small size of the Ag2Se nanoparticles in RGO‐Ag2Se was related to the use of ultrasonication during their formation, revealing that this approach is attractive to form po‐rous RGO‐Ag2Se materials with high photocatalytic activity under visible light.

  15. Application of coals as sorbents for the removal of Cr from aqueous waste streams

    Lakatos, J.; Brown, S.D.; Snape, C.E. [University of Miskolc, Miskolc (Hungary). Dept. of Analytical Chemistry


    The study reported further understanding of how various electron transfer processes operate for Cr(VI) with a view to using coals for the removal of Cr(VI) from waste streams. Skye peat, Spanish and German lignites, UK high and low volatility bituminous coals and an activated carbon were used. After treatment to remove exchangeable cations, ion exchange experiments were conducted in 0.1 M acetic acid-sodium acetate (1:1) buffer and 0.05 M sulphuric acid solutions and the slurries were agitated once a day. The ion concentrations in the solutions were determined by flame atomic absorption spectroscopy. The Cr(VI) renaming in solution was determined by the standard calorimetric 1,5-diphenylcarbazide method. Peat and low rank (Spanish Mequinenza) coal exhibited a larger capacity for Cr(VI) removal than bituminous coal. Redox mechanisms are operative coupled with the oxidation of the coal and peat surfaces. Desorption of Cr(III) formed by reduction which occurs in strongly acidic media also needs to be considered. 1 ref., 3 figs.

  16. Effects of Cu(II) complexes on photosynthesis in spinach chloroplasts. Aqua(aryloxyacetato)copper(II) complexes.

    Král'ová, K; Sersen, F; Blahová, M


    The inhibitory effect of 14 aqua(aryloxyacetato) copper(II) complexes on oxygen evolution rate in spinach chloroplasts has been investigated. The inhibitory effect of these effectors on photosynthesis was confirmed by Hill reaction as well as by EPR and fluorescence spectroscopies. The results of the EPR study showed that the sites of action of the studied effectors are Z+ and Y+ intermediates at the donor side of the photosystem (PS) 2. The EPR study also showed that another site of action is the oxygen evolving complex, namely its manganese cluster. The above suggestions were supported by the results of the fluorescence study as well. Based on the restoring of the photosynthetic electron transport to 2,6-dichlorophenol-indophenol in chloroplasts inhibited by the studied Cu(II) complexes using sym-diphenylcarbazide it can be assumed that the own core of PS2 (P680) and a part of the electron transport chain-at least up to plastoquinone-remain intact.

  17. Bioremediation of Hexavalent Chromium Pollution by Sporosarcina saromensis M52 Isolated from Offshore Sediments in Xiamen, China

    ZHAO Ran; WANG Bi; CAI Qing Tao; LI Xiao Xia; LIU Min; HU Dong; GUO Dong Bei; WANG Juan; FAN Chun


    ObjectiveCr(VI) removal from industrial effluents and sediments has attracted the attention of environmental researchers. In the present study, we aimed to isolate bacteria for Cr(VI) bioremediation from sediment samples and to optimize parameters of biodegradation. MethodsStrains with the ability to tolerate Cr(VI) were obtained by serial dilution and spread plate methods and characterized by morphology, 16S rDNA identification, and phylogenetic analysis. Cr(VI) was determined using the 1,5-diphenylcarbazide method, and the optimum pH and temperature for degradation were studied using a multiple-factor mixed experimental design. Statistical analysis methods were used to analyze the results. ResultsFifty-five strains were obtained, and one strain (Sporosarcina saromensisM52; patent application number: 201410819443.3) having the ability to tolerate 500 mg Cr(VI)/L wasselected to optimize the degradation conditions. M52 was found be able to efficiently remove 50-200 mg Cr(VI)/L in 24 h, achieving the highest removal efficiency at pH 7.0-8.5 and 35°C. Moreover, M52 could completely degrade 100 mg Cr(VI)/L at pH 8.0 and35 °C in 24 h. The mechanism involved in the reduction of Cr(VI) was considered to be bioreduction rather than absorption. ConclusionThe strong degradation ability ofS. saromensis M52 and its advantageous functional characteristics support the potential use of this organism for bioremediation ofheavy metal pollution.

  18. Determination of hexavalent chromium concentration in industrial waste incinerator stack gas by using a modified ion chromatography with post-column derivatization method.

    Miyake, Yuichi; Tokumura, Masahiro; Iwazaki, Yuta; Wang, Qi; Amagai, Takashi; Horii, Yuichi; Otsuka, Hideyuki; Tanikawa, Noboru; Kobayashi, Takeshi; Oguchi, Masahiro


    An ion chromatography with post-column derivatization with 1,5-diphenylcarbazide (IC-DPC) analytical method was modified to enable measurement of trace-level hexavalent chromium (Cr(VI)) in air. One of the difficulties in determining trace levels of Cr(VI) in air with conventional IC-DPC methods is co-elution of the solvent and ion peaks due to high concentrations of ionic compounds in the extract. However, by using gradient elution rather than isocratic elution we were able to fully resolve the Cr(VI) ion peak from the solvent peak without the need for diluting the extract, which would have reduced the minimum quantifiable level of the method. With this method, we were able to detect Cr(VI) in air at concentrations of 5.3ng/m(3) (assuming a sampling volume of 1m(3) and a final solution volume of 10mL). Recovery tests at three different concentrations of Cr(VI) (50, 250, 1000ng) were performed with or without fly ash; recovery rates at all the concentrations of Cr(VI), with or without fly ash, ranged from 68% to 110% (mean±relative standard deviation, 96%±11%), and there were no differences in recovery rates with respect to the presence or absence of fly ash. Finally, we used the developed method to determine the concentration of Cr(VI) in stack gases collected from eight industrial waste incinerators located in Japan. The concentration of Cr(VI) in the stack gases ranged from below the method quantification limit to 3100ng/m(3). The highest concentrations of Cr(VI) detected in the stack gases were two to three orders of magnitude higher than that in ambient air in Japan. Copyright © 2017 Elsevier B.V. All rights reserved.

  19. Determination of hexavalent chromium in exhaled breath condensate and environmental air among chrome plating workers

    Goldoni, Matteo [Laboratory of Industrial Toxicology, Department of Clinical Medicine, Nephrology and Health Sciences, University of Parma, Via Gramsci 14, 43100 Parma (Italy); National Institute of Occupational Safety and Prevention, Research Centre at University of Parma, Parma (Italy); Caglieri, Andrea [Laboratory of Industrial Toxicology, Department of Clinical Medicine, Nephrology and Health Sciences, University of Parma, Via Gramsci 14, 43100 Parma (Italy); Poli, Diana [Laboratory of Industrial Toxicology, Department of Clinical Medicine, Nephrology and Health Sciences, University of Parma, Via Gramsci 14, 43100 Parma (Italy); National Institute of Occupational Safety and Prevention, Research Centre at University of Parma, Parma (Italy); Vettori, Maria Vittoria [Laboratory of Industrial Toxicology, Department of Clinical Medicine, Nephrology and Health Sciences, University of Parma, Via Gramsci 14, 43100 Parma (Italy); National Institute of Occupational Safety and Prevention, Research Centre at University of Parma, Parma (Italy); Corradi, Massimo [Laboratory of Industrial Toxicology, Department of Clinical Medicine, Nephrology and Health Sciences, University of Parma, Via Gramsci 14, 43100 Parma (Italy); National Institute of Occupational Safety and Prevention, Research Centre at University of Parma, Parma (Italy); Apostoli, Pietro [Laboratory of Industrial Hygiene, Department of Experimental and Applied Medicine, University of Brescia (Italy); Mutti, Antonio [Laboratory of Industrial Toxicology, Department of Clinical Medicine, Nephrology and Health Sciences, University of Parma, Via Gramsci 14, 43100 Parma (Italy)]. E-mail:


    Chromium speciation has attracted attention because of the different toxicity of Cr(III), which is considered relatively non-toxic, and Cr(VI), which can cross cell membranes mainly as a chromate anion and has been classified as a class I human carcinogen. The aims of the present study were to measure soluble Cr(VI) levels in environmental samples, to develop a simple method of quantifying Cr(VI) in exhaled breath condensate (EBC), and to follow the kinetics of EBC Cr(VI) in chrome plating workers. Personal air samples were collected from 10 chrome platers; EBC was collected from the same workers immediately after the work shift on Tuesday and before the work shift on the following Wednesday. Environmental and EBC Cr(VI) levels were determined by means of colorimetry and electrothermal absorption atomic spectrometry, respectively. The method of detecting Cr(VI) in environmental air was based on the extraction of the Cr(VI)-diphenylcarbazide (Cr(VI)-DPC) complex in 1-butanol, whereas EBC Cr(VI) was determined using a solvent extraction of Cr(VI) as an ion pair with tetrabutylammonium ion, and subsequent direct determination of the complex (Cr(VI)-DPC) in EBC. Kinetic data showed that airborne Cr(VI) was reduced by 50% in airway lining fluid sampled at the end of exposure and that there was a further 50% reduction after about 15 h. The persistence of Cr(VI) in EBC supports the use of EBC in assessing target tissue levels of Cr(VI)

  20. A microfluidic paper-based analytical device for rapid quantification of particulate chromium

    Rattanarat, Poomrat [Electrochemistry and Optical Spectroscopy Research Unit (EOSRU), Department of Chemistry, Faculty of Science, Chulalongkorn University, Patumwan, Bangkok 10330 (Thailand); Dungchai, Wijitar [Department of Chemistry, Faculty of Science, King Mongkut' s University of Technology Thonburi, 91 Prachautid Road, Thungkru, Bangkok 10140 (Thailand); Cate, David M. [School of Biomedical Engineering, Colorado State University, Fort Collins, CO 80523 (United States); Siangproh, Weena [Department of Chemistry, Faculty of Science, Srinakharinwirot University, Sukhumvit 23, Wattana, Bangkok 10110 (Thailand); Volckens, John, E-mail: [Department of Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, CO 80523 (United States); Chailapakul, Orawon, E-mail: [Electrochemistry and Optical Spectroscopy Research Unit (EOSRU), Department of Chemistry, Faculty of Science, Chulalongkorn University, Patumwan, Bangkok 10330 (Thailand); National Center of Excellence for Petroleum, Petrochemicals and Advanced Materials, Chulalongkorn University, Patumwan, Bangkok 10330 (Thailand); Henry, Charles S., E-mail: [School of Biomedical Engineering, Colorado State University, Fort Collins, CO 80523 (United States); Department of Chemistry, Colorado State University, Fort Collins, CO 80523 (United States)


    Graphical abstract: -- Highlights: •Cr detection using a paper-based analytical device. •Analysis of total Cr levels in particulate matter was achieved. •Method for on-paper oxidation of Cr to Cr(VI) using Ce(IV) was established. -- Abstract: Occupational exposure to Cr is concerning because of its myriad of health effects. Assessing chromium exposure is also cost and resource intensive because the analysis typically uses sophisticated instrumental techniques like inductively coupled plasma-mass spectrometry (ICP-MS). Here, we report a novel, simple, inexpensive microfluidic paper-based analytical device (μPAD) for measuring total Cr in airborne particulate matter. In the μPAD, tetravalent cerium (Ce(IV)) was used in a pretreatment zone to oxidize all soluble Cr to Cr(VI). After elution to the detection zone, Cr(VI) reacts with 1,5-diphenylcarbazide (1,5-DPC) forming 1,5-diphenylcarbazone (DPCO) and Cr(III). The resulting Cr(III) forms a distinct purple colored complex with the DPCO. As proof-of-principle, particulate matter (PM) collected on a sample filter was analyzed with the μPAD to quantify the mass of total Cr. A log-linear working range (0.23–3.75 μg; r{sup 2} = 0.998) between Cr and color intensity was obtained with a detection limit of 0.12 μg. For validation, a certified reference containing multiple competing metals was analyzed. Quantitative agreement was obtained between known Cr levels in the sample and the Cr measured using the μPAD.

  1. Bioadsorción de Cromo (VI en Solución Acuosa por la Biomasa Celular de Cryptococcus neoformans y Helminthosporium sp Biosorption of Chromium (VI from Aqueous Solutions by Fungal Biomass of Cryptococcus neoformans and Helminthosporium sp

    I. Acosta


    Full Text Available Se determinó la bioadsorción de Cromo (VI en solución por la biomasa celular de la levadura capsulada Cryptococcus neoformans y del hongo micelial Helminthosporium sp, por el método colorimétrico de la difenilcarbazida. La biomasa de C. neoformans fue más eficiente en la remoción de Cromo (VI en solución (98% que la de Helminthosporium sp (65%. La mayor bioadsorción para C. neoformans fue a pH=2.0 +/- 0.2, mientras que para Helminthosporium sp fue a pH=4.0 +/- 0.2, ambas a 28oC durante 24 horas con 0.2 mg/L de biomasa celular. Se concluye que las biomasas fúngicas remueven eficientemente Cromo (VI en solución y pueden utilizarse para descontaminar nichos acuáticos contaminados con este metal.A determination was made on the biosorption of dissolved Chromium (VI using cellular biomass of the encapsulated yeast Cryptococcus neoformans and the mycelial fungus Helminthosporium sp. using a diphenylcarbazide colorimetric method. The C. neoformans biomass was more efficient in removing Chromium (VI from solution (98% than the Helminthosporium sp. (65%. The highest biosorption for C. neoformans was at pH 2.0 + 0.02, while for Helminthosporium sp this occurred at pH 4.0 + 0.2 , both at 28°C for 24 h employing 0.2 mg/L of cellular biomass. It is concluded that the fungal biomasses efficiently removed Chromium (VI from solution and could be used for decontamination of aquatic habitats polluted with this metal.

  2. Airborne exposure to inhalable hexavalent chromium in welders and other occupations: Estimates from the German MEGA database.

    Pesch, Beate; Kendzia, Benjamin; Hauptmann, Kristin; Van Gelder, Rainer; Stamm, Roger; Hahn, Jens-Uwe; Zschiesche, Wolfgang; Behrens, Thomas; Weiss, Tobias; Siemiatycki, Jack; Lavoué, Jerome; Jöckel, Karl-Heinz; Brüning, Thomas


    This study aimed to estimate occupational exposure to inhalable hexavalent chromium (Cr(VI)) using the exposure database MEGA. The database has been compiling Cr(VI) concentrations and ancillary data about measurements at German workplaces. We analysed 3659 personal measurements of inhalable Cr(VI) collected between 1994 and 2009. Cr(VI) was determined spectrophotometrically at 540 nm after reaction with diphenylcarbazide. We assigned the measurements to pre-defined at-risk occupations using the information provided about the workplaces. Two-thirds of the measurements were below the limit of quantification (LOQ) and multiply imputed according to the distribution above LOQ. The 75th percentile value was 5.2 μg/m(3) and the 95th percentile was 57.2 μg/m(3). We predicted the geometric mean for 2h sampling in the year 2000, and the time trend of Cr(VI) exposure in these settings with and without adjustment for the duration of measurements. The largest dataset was available for welding (N = 1898), which could be further detailed according to technique. The geometric means were above 5 μg/m(3) in the following situations: spray painting, shielded metal arc welding, and flux-cored arc welding if applied to stainless steel. The geometric means were between 1 μg/m(3) and 5 μg/m(3) for gas metal arc welding of stainless steel, cutting, hard-chromium plating, metal spraying and in the chemical chromium industry. The exposure profiles described here are useful for epidemiologic and industrial health purposes. Exposure to Cr(VI) varies not only between occupations, but also within occupations as shown for welders. In epidemiologic studies, it would be desirable to collect exposure-specific information in addition to the job title.

  3. Chromium availability in ultramafic soils from New Caledonia.

    Becquer, T; Quantin, C; Sicot, M; Boudot, J P


    The sources and potential availability of chromium (Cr) on soils formed on ultramafic rocks were investigated with mineralogical studies and selective chemical extractions. Soil solutions were collected in the field (i) along a soil toposequence under natural vegetation with ceramic cups; (ii) under grass in a mandarin trees plantation with tension-free tube lysimeters. On selected soil solutions, the Cr(VI) was determined colorimetrically with the s-diphenylcarbazide method and total Cr by ICP-AES and speciation of Cr(VI) was performed with the MINEQL+ V 4.5 software. The main mineralogical sources of Cr were Cr-substituted goethite and chromite. Up to 90 mg kg(-1) of Cr was extracted by KH(2)PO(4), whereas KCl extractable Cr was very low, indicating that exchangeable Cr was mainly in the highly toxic Cr(VI) form in these soils. Under natural vegetation, the Cr concentrations in the soil solutions remained relatively low (<20 microg l(-1)) due to the high retention of the Cr(VI) anions by Fe-oxides. The Cr concentrations were larger in well aerated colluvial soils, where high levels of Mn-oxides are able to oxidize Cr(III) to Cr(VI), than in piedmont soil where the Mn-oxide content is lower, or in alluvial soils from the lowlands, where waterlogging occurs. Cr concentrations reached 700 microg l(-1) in the field that was fertilized with high amount of phosphorus, due to the exchange of Cr(VI) with phosphate. In such conditions, toxicity phenomena for crops can be expected.

  4. Hydrogen peroxide inhibits photosynthetic electron transport in cells of cyanobacteria.

    Samuilov, V D; Bezryadnov, D B; Gusev, M V; Kitashov, A V; Fedorenko, T A


    The effect of H2O2 on photosynthetic O2 evolution and photosynthetic electron transfer in cells of cyanobacteria Anabaena variabilis and Anacystis nidulans was studied. The following experiments were performed: 1) directly testing the effect of exogenous H2O2; 2) testing the effect of intracellular H2O2 generated with the use of methyl viologen (MV); 3) testing the effect of inhibiting intracellular H2O2 decomposition by salicylic acid (SA) and 3-amino-1,2,4-triazole (AT). H2O2 inhibited photosynthetic O2 evolution and light-induced reduction of p-benzoquinone (BQ) + ferricyanide (FeCy) in the Hill reaction. The I50 value for H2O2 was ~0.75 mM. Photosynthetic electron transfer in the cells treated with H2O2 was not maintained by H2O2, NH2OH, 1,5-diphenylcarbazide, tetraphenylboron, or butylated hydroxytoluene added as artificial electron donors for Photosystem (PS) II. The H2O --> CO2, H2O --> MV (involving PSII and PSI) and H2O --> BQ + FeCy (chiefly dependent on PSII) electron transfer reactions were inhibited upon incubation of the cells with MV, SA, or AT. The N,N,N,N-tetramethyl-p-phenylenediamine --> MV (chiefly dependent on PSI) electron transfer was inhibited by SA and AT but was resistant to MV. The results show that H2O2 inhibits photosynthetic electron transfer. It is unlikely that H2O2 could be a physiological electron donor in oxygenic photosynthesis.

  5. Selective sampling and measurement of Cr (VI) in water with polyquaternary ammonium salt as a binding agent in diffusive gradients in thin-films technique

    Chen, Hong, E-mail: [College of Chemistry, Chemical Engineering and Food Safety, Bohai University (China); Research Institute of Food Science, Bohai University (China); Food Safety Key Lab of Liaoning Province, Jinzhou 121013 (China); Zhang, Yang-Yang; Zhong, Ke-Li; Guo, Lian-Wen [College of Chemistry, Chemical Engineering and Food Safety, Bohai University (China); Research Institute of Food Science, Bohai University (China); Food Safety Key Lab of Liaoning Province, Jinzhou 121013 (China); Gu, Jia-Li [College of Chemistry, Chemical Engineering and Food Safety, Bohai University (China); Bo, Le; Zhang, Meng-Han [College of Chemistry, Chemical Engineering and Food Safety, Bohai University (China); Research Institute of Food Science, Bohai University (China); Food Safety Key Lab of Liaoning Province, Jinzhou 121013 (China); Li, Jian-Rong, E-mail: [College of Chemistry, Chemical Engineering and Food Safety, Bohai University (China); Research Institute of Food Science, Bohai University (China); Food Safety Key Lab of Liaoning Province, Jinzhou 121013 (China)


    Graphical abstract: - Highlights: • We develop a new DGT device for in situ sampling Cr (VI) in water. • Polyquaternary ammonium salt (PQAS) was used as binding agent of DGT device. • Cr (VI) can be accumulated in the PQAS binding phase whereas Cr (III) cannot. • The DGT performance was independent of pH 3–12 and ionic strength 1 × 10{sup −3}–1 mol L{sup −1}. - Abstract: A diffusive gradients in thin films (DGT) device with polyquaternary ammonium salt (PQAS) as a novel binding agent (PQAS DGT) combined with graphite furnace atomic absorption spectrometry (GFAAS) was developed for the selective sampling and measurement of Cr (VI) in water. The performance of PQAS DGT was independent of pH 3–12 and ionic strength from 1 × 10{sup −3} to 1 mol L{sup −1}. DGT validation experiments showed that Cr (VI) was measured accurately as well as selectively by PQAS DGT, whereas Cr (III) was not determined quantitatively. Compared with diphenylcarbazide spectrophotometric method (DPC), the measurement of Cr (VI) with PQAS DGT was agreement with that of DPC method in the industrial wastewater. PQAS-DGT device had been successfully deployed in local freshwater. The concentrations of Cr (VI) determined by PQAS DGT coupled with GFAAS in Nuer River, Ling River and North Lake were 0.73 ± 0.09 μg L{sup −1}, 0.50 ± 0.07 μg L{sup −1} and 0.61 ± 0.07 μg L{sup −1}, respectively. The results indicate that PQAS DGT device can be used for the selective sampling and measurement Cr (VI) in water and its detection limit is lower than that of DPC method.

  6. Protein expression on Cr resistant microorganism using electrophoresis method



    Full Text Available Fatmawati U, Suranto, Sajidan. 2009. Protein expression on Cr resistant microorganism using electrophoresis method. Nusantara Bioscience 1: 31-37. Hexavalent chromium (Cr(VI is known as toxic heavy metals, so the need is reduced to Cr(III is much less toxicity. Pseudomonas aeruginosa, Pseudomonas putida, Klebsiella pneumoniae, Pantoea sp. and Saccharomyces cerevisiae are resistant Cr(VI microorganism and have ability to reduce Cr(VI. The aim of this research is to know ability of microorganism to reduce Cr(VI and to know protein band pattern between Cr(VI resistant microorganism and non resistant microorganism which inoculated on LB broth. SDS-PAGE was used to indentify protein expression. While, Cr(VI concentration was identified by 1.5 diphenylcarbazide method. The quantitative data was analyzed by two factorial ANOVA that continued with DMRT at 1% level test. The qualitative data i.e. protein expression analyzed by relative mobility (Rf. The results showed that the ability of microorganisms to reduce Cr(VI at initial concentration of 0.5 ppm, 1 ppm, 5 ppm and 10 ppm may vary, the average percentage of the ability of each microorganism in reducing Cr(VI is P. putida (65% > S. cerevisiae (64.45% >. P. aeruginosa (60.73% > Pantoea sp. (50.22% > K. pneumoniae (47.82% > without microorganisms (34.25%. The adding microorganisms have significantly influenced toward reduction of Cr(VI. The SDS-PAGE shows that protein expression between resistant and not resistant microorganisms are no different, but resistant microorganisms have more protein (protein band is thicker.

  7. Correlation between bulk- and surface chemistry of Cr-tanned leather and the release of Cr(III) and Cr(VI)

    Hedberg, Yolanda S., E-mail: [KTH Royal Institute of Technology, School of Chemical Science and Engineering, Department of Chemistry, Division of Surface and Corrosion Science, SE-10044 Stockholm (Sweden); Institute of Environmental Medicine, Karolinska Institutet, Box 210, SE-17177 Stockholm (Sweden); Lidén, Carola, E-mail: [Institute of Environmental Medicine, Karolinska Institutet, Box 210, SE-17177 Stockholm (Sweden); Odnevall Wallinder, Inger, E-mail: [KTH Royal Institute of Technology, School of Chemical Science and Engineering, Department of Chemistry, Division of Surface and Corrosion Science, SE-10044 Stockholm (Sweden)


    Graphical abstract: - Highlights: • Released reducing/complexing leather-specific species can reduce released Cr(VI). • No co-released species enable the formation of Cr(VI) in solution. • The major Cr species released from leather in phosphate buffer was Cr(III) (>82%). • No Cr(VI) was released into artificial sweat. - Abstract: About 1–3% of the adult general population in Europe is allergic to chromium (Cr). The assessment of the potential release of Cr(III) and Cr(VI) from leather is hence important from a human health and environmental risk perspective. The Cr(VI) content in leather was recently restricted in the European Union. The aim of this study was to assess possible correlations between the bulk and surface chemistry of leather, released Cr(III) and Cr(VI), and capacities of co-released leather specific species to reduce and complex released Cr. Four differently tanned leathers were characterized by scanning electron microscopy with energy dispersive spectroscopy, X-ray photoelectron spectroscopy, attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy, and the diphenylcarbazide colorimetric method. Their characteristics were compared with results on Cr(III) and Cr(VI) release into artificial sweat (ASW, pH < 6.5) and phosphate buffer (PB, pH 7.5–8.0), measured by means of spectrophotometry and atomic absorption spectroscopy. Co-released leather-specific species were shown to reduce Cr(VI), both in ASW and in PB. Their reduction capacities correlated with findings of the surface content of Cr and of released Cr. Leather samples without this capacity, and with less aromatic surface groups visible by ATR-FTIR, revealed Cr(VI) both at the surface and in solution (PB)

  8. Study on the activity of electron transfer of photosystem Ⅱ removed manganese cluster by using exogenous electron carriers%利用外源电子载体研究去除锰簇的光系统Ⅱ的电子传递活性

    由万胜; 黄海丽; 康阳; 姚明东; 陈钧


    光系统Ⅱ(PSⅡ)利用锰簇(OEC)氧化水分解并将电子通过类囊体膜上的电子传递链传递到外源电子受体侧。但是去除锰簇的光系统Ⅱ(T ris‐Wash BBY )是否具有电子传递能力仍是一个值得研究的问题。因此本文引进外源电子供体1,5‐二苯基卡巴肼(DPC)代替锰簇向电子受体侧提供电子,研究Tris‐Wash BBY的电子转移活性。实验表明T ris‐Wash BBY在光照的条件下可以将 DPC的电子传递给外源电子受体2,6‐二氯酚靛酚(DCPIP),并且利用紫外可见光谱的方法,通过分析外源电子受体DCPIP的还原量来表征T ris‐Wash BBY和BBY的电子传递活性。%Photosystem Ⅱ (BBY) could split water on manganese cluster (OEC) and transfer elec‐trons to exogenous electron acceptor side through the thylakoid membrane electron transport chain . But it is still worthy to study whether photosystem Ⅱ (Tris‐Wash BBY) which removed the manga‐nese cluster has capability of the electron transfer .Therefore ,this article introduces an exogenous e‐lectron donor 1 ,5‐Diphenylcarbazide (DPC) insteading of manganese cluster to provide electron for measuring the activity of electron transfer of Tris‐Wash BBY .The results show that electrons could transport from DPC to DCPIP under illumination in Tris‐Wash BBY .We could characterize electron transfer activity of T ris‐Wash BBY and BBY by analyzing the reduction amount of DCPIP based on UV‐visible spectroscopy methods .

  9. 铬(Ⅵ)-过氧化氢-中性红体系催化荧光光度法测定工业废水中铬(Ⅵ)%Determination of chromim(Ⅵ) in industry wastewater by catalytic fluorescence spectrophotometry in Cr(Ⅵ)-hydrogen peroxide-neutral red system

    刘卫洁; 王胜利; 高玉红; 冯存霞


    Trace chromium (VD had catalytic effect on hydrogen peroxide - neutral red reaction system in diluted sulfuric acid medium, enhancing the fluorescence intensity. Moreover, the mass concentration of Cr (Ⅵ) in the range of 8. 0 — 48. 0 μg/L showed linearity to the change of fluorescence intensity (△F). Based on this, a new determination method of Cr (Ⅵ) by catalytic fluorescence spectrophotome-try was established- The excitation wavelength (λex) and emission wavelength (λex) of this system was 547 nm and 648 nm, respectively. The apparent rate constant (k) and reaction activation energy (Ea) of catalytic reaction, was 8. 05×10-2s-1 and 31. 47 kJ · mol-1, respectively. The detection limit of Cr (Ⅵ) was 4 μg/L. The method was applied to the determination of Cr (Ⅵ) in synthetic water sample and metallurgical industry wastewater. The found results were consistent with those obtained by di-phenylcarbazide spectrophotometry. The relative standard deviation (RSD, n=5) was smaller than 4 %.%在稀硫酸介质中,痕量Cr(Ⅵ)对过氧化氢-中性红的反应体系具有催化作用,使体系的荧光强度增强,且Cr(Ⅷ的质量浓度在8.0~48.0 μg/L范围内与荧光强度的改变值(△F)呈线性关系,据此建立了催化荧光光度法测定Cr(Ⅵ)的新方法.该体系的激发和发射波长(λex和λem)分别为547 nm和648 nm.通过实验测得催化反应的表观速率常数k和反应活化能Ea分别为8.05×10-2s-1和31.47 kJ·mol-1,Cr(Ⅵ)的检出限为4 μg/L.将本方法用于合成水样和冶金工业废水中Cr(Ⅳ)的测定,所得结果与二苯碳酰二肼分光光度法测得值吻合,相对标准偏差(RSD,n=5)小于4%.

  10. Hybrid flow analyzer for automatic hollow-fiber-assisted ionic liquid-based liquid-phase microextraction with in-line membrane regeneration.

    Nitiyanontakit, Sira; Varanusupakul, Pakorn; Miró, Manuel


    The proof-of-concept of a new methodology for in-line hollow-fiber (HF)-assisted three-phase liquid-phase microextraction (LPME) allowing for handling of the feed and acceptor aqueous solutions and of minute volumes of the organic extracting phase in a programmable flow mode is reported in this paper. The flow analyzer fosters in-line anchoring of ionic-liquid-laden extracting solution (10 % (v/v) methyltrioctyl ammonium chloride in kerosene) in the pores of a single-strand microporous polypropylene HF, and regeneration of the liquid-phase membrane itself for each individual analysis cycle in a fully automated mode. Using hexavalent chromium as a model analyte and 1,5-diphenylcarbazide as a chromogenic probe in the acceptor solution, the flow-based HF-LPME hyphenated system was harnessed to the clean-up of troublesome samples (viz., domestic wastewater and soil leachates) with concomitant enrichment of target species. Distinct extraction modes and chemistries were assessed for enhanced Cr(VI) permeability. A single sample plug was subjected to a twofold backward-forward flow extraction so as to decrease the thickness of the boundary layer at the HF shell side for improved extraction efficiency. Under the optimized physicochemical variables, a limit of detection of 4.6 μg L(-1) Cr(VI), a dynamic linear range of up to 500 μg L(-1) and intermediate precision better than 10 % were obtained for a sample volume of 2.8 mL buffered at pH 4 and a volume of organic extractant of 120 μL, with an enrichment factor of ca. 11 for a sample residence time in the donor compartment of merely 4.5 min. Analyte recoveries in domestic wastewaters were ≥83 % using external calibration with relative standard deviations better than 14 %, thereby demonstrating the expedient clean-up of samples with elevated content of dissolved organic carbon. The automatic HF-LPME method was validated in terms of bias against the SRM 2701 (NIST soil) preceded by the EPA alkaline digestion method 3060A

  11. Redução de cromo hexavalente por bactérias isoladas de solos contaminados com cromo Reduction of hexavlent chromium by isolated bacteria of contaminated soils with chromium

    Daniele Conceição


    Full Text Available A redução do Cr(VI para Cr(III diminui a toxidade deste metal no ambiente, uma vez que o Cr(III é insolúvel às membranas biológicas. Assim, a redução microbiana do Cr(VI é uma alternativa para reduzir os impactos ambientais causados por este metal, utilizado em diversos processos industriais. O objetivo deste trabalho foi selecionar microrganismos a partir de solo contaminado com cromo e caracterizar sua capacidade de redução do Cr(VI durante o crescimento celular. A atividade de redução do Cr(VI pelos isolados foi quantificada com o reagente de s-difenilcarbazida. No isolamento, foram obtidas 20 bactérias resistentes a cromo(VI; seis destas foram capazes de reduzir acima de 100mg L-1 Cr(VI em 24 horas. As bactérias selecionadas foram eficientes na redução do Cr(VI e apresentam potencial para outros estudos, visando à aplicação em processos de biorremediação.The reduction of Cr(VI to Cr(III decrease the toxic effect of this metal in the environment, because Cr(III is insoluble to the biological membranes. The microbial reduction of Cr(VI it is an alternative to reduce the environmental impacts caused by this metal used in several industrial processes. The objective of this research was to select microorganisms from chromium contaminated soil and to characterize their ability to reduce Cr(VI. The activity of reduction of Cr(VI for the isolated was quantified with s-diphenylcarbazide. A group of 20 chromium resistant bacteria were isolated; six of these were able to reduce 100mg L-1 Cr(VI in 24 hours. The isolated bacteria, from contaminated soil can remediate chromate and presented potential for other studies seeking their application in bioremediation processes.

  12. Study of cis- and trans-uranium elements by paper chromatography and electrophoresis; Contribution a l'etude des elements cis- et trans-uraniens par chromatographie sur papier et electrophorese

    Clanet, F. [Commissariat a l' Energie Atomique, 92 - Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires


    In this work, the field of application of paper chromatography and electrophoresis in inorganic chemistry has been extended to elements 90 to 96 in hydrochloric and nitric acid solution. Results obtained concern the following points: 1) - Characterization of the valency states of Np and of Pu using coloured reactions on chromatograms and electrophoregrams. The valency IV is characterized by alizarin, arsenazo-I and thorin-I, whilst diphenylcarbazide is used for the hexavalent state. 2) - Paper chromatography: by using as eluent, mixtures of equal parts of aqueous HCl and HNO{sub 3} solutions and of alcohols (methanol, ethanol and n-butanol), the R{sub f} values of elements 90 to 96 have been determined. It has been possible to deduce certain conclusions concerning the complexing of these elements by Cl{sup -} and NO{sub 3}{sup -} ions. 3) - We have developed an electrophoretic technique on cellulose acetate membranes in order to separate the charged species formed by the elements 90 to 96 in HCl and HNO{sub 3} solutions from 1 to 12 M. Mobility curves have been obtained. It appears from our results that the tendency for the elements considered to form anionic complexes follows the order of the ionic potentials when the valency state is four; this order is reversed for the valency three. The ions Cl{sup -} have a smaller tendency to form complexes than the NO{sub 3}{sup -} ions with respect to these elements in their oxidation state III or IV, but the reverse phenomenon is observed for U{sup VI} and Pu{sup VI}. Finally, the complexing of the cations Pu{sup 4+} and PuUO{sub 2}{sup 2+} by NO{sub 3}{sup -} follows the order of the ionic potentials but occurs in the reverse order for Cl{sup -} ions. 4) - Various analytical applications are considered: separation of the various elements from each other and separation of the valency states of Np and of Pu. (author) [French] Dans cette etude, le champ d'application de la chromatographie sur papier et de l

  13. Accumulation and hyperaccumulation of copper in plants

    Adam, V.; Trnkova, L.; Huska, D.; Babula, P.; Kizek, R.


    have adapted on such stress. The aim of this study is to investigate the behaviour of copper in plants and to assess its potential effect on the surrounding environment. To detect copper in biological samples electrochemical methods were employed particularly differential pulse voltammetry (DPV). Copper gave signals at 0.02 V measured by DPV. The obtained calibration dependence was linear (R2 = 0.995). Further, this method was utilized for determination of copper in real soil samples obtained from previously mentioned heavy-metal-polluted mining area. The content varied within range from tens to hundreds of mg of copper per kg of the soil. Moreover, we focused on investigation of copper influence on seedlings of Norway spruce. The seedlings were treated with copper (0, 0.1, 10 and 100 mM) for four weeks. We observed anatomical-morphological changes and other biochemical parameters in plants. We determined that seedlings synthesized more than 48 % protective thiols (glutathione and phytochelatins) compared to control ones. We investigated copper distribution in plant tissues by diphenylcarbazide staining. We found out that copper is highly accumulated in parenchymal stalk cells. In needles, change in auto-fluorescence of parenchymal cells of mesoderm similarly to endodermis cells. Besides, we analyzed samples of plants from the polluted area (spruce, pin, birch). The data obtained well correlated with previously mentioned. Acknowledgement The work on this experiment was supported by grant: INCHEMBIOL MSM0021622412.