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Sample records for cr vi reduction

  1. Nonspecificity of bacterial reduction of Cr(VI)

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    Gvozdyak, P.I.; Mogilevich, N.F.; Ryl' skiy, A.F.; Grishchenko, N.I.

    1985-03-01

    Eight different genera of gram-positive and negative bacteria were tested for their ability to carry out reduction of Cr(VI) to Cr(III). The results demonstrated that in addition to Pseudomonas the other genera capable of similar enzymatic activity were Achromobacter, Bacillus and Micrococcus. These observations indicate that reduction of Cr(VI) is not a unique feature of Pseudomonas alone, and that the availability of other bacteria with similar metabolic potential expands the possibility of their utilization in water treatment and possibly in metallurgical enrichment biotechnology. 15 references.

  2. Dissimilatory Reduction of Cr(VI), Fe(III), and U(VI) by Cellulomonas Isolates

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    Smith, William Aaron; Apel, William Arnold; Peyton, B. M.; Petersen, J. N.; Sani, R.

    2002-10-01

    The reduction of Cr(VI), Fe(III), and U(VI) was studied using three recently isolated environmental Cellulomonas sp. (WS01, WS18, and ES5) and a known Cellulomonas strain (Cellulomonas flavigena ATCC 482) under anaerobic, non-growth conditions. In all cases, these cultures were observed to reduce Cr(VI), Fe(III), and U(VI). In 100 h, with lactate as electron donor, the Cellulomonas isolates (500 mg/l total cell protein) reduced nitrilotriacetic acid chelated Fe(III) [Fe(III)-NTA] from 5 mM to less than 2.2 mM, Cr(VI) from 0.2 mM to less than 0.001 mM, and U(VI) from 0.2 mM to less than 0.12 mM. All Cellulomonas isolates also reduced Cr(VI), Fe(III), and U(VI) in the absence of lactate, while no metal reduction was observed in either the cell-free or heat-killed cell controls. This is the first report of Cellulomonas sp. reducing Fe(III) and U(VI). Further, this is the first report of Cellulomonas spp. coupling the oxidation of lactate, or other unknown electron donors in the absence of lactate, to the reduction of Cr(VI), Fe(III), and U(VI).

  3. Dissimilatory reduction of Cr(VI), Fe(III), and U(VI) by Cellulomonas isolates.

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    Sani, R K; Peyton, B M; Smith, W A; Apel, W A; Petersen, J N

    2002-10-01

    The reduction of Cr(VI), Fe(III), and U(VI) was studied using three recently isolated environmental Cellulomonas sp. (WS01, WS18, and ES5) and a known Cellulomonas strain ( Cellulomonas flavigena ATCC 482) under anaerobic, non-growth conditions. In all cases, these cultures were observed to reduce Cr(VI), Fe(III), and U(VI). In 100 h, with lactate as electron donor, the Cellulomonas isolates (500 mg/l total cell protein) reduced nitrilotriacetic acid chelated Fe(III) [Fe(III)-NTA] from 5 mM to less than 2.2 mM, Cr(VI) from 0.2 mM to less than 0.001 mM, and U(VI) from 0.2 mM to less than 0.12 mM. All Cellulomonas isolates also reduced Cr(VI), Fe(III), and U(VI) in the absence of lactate, while no metal reduction was observed in either the cell-free or heat-killed cell controls. This is the first report of Cellulomonas sp. reducing Fe(III) and U(VI). Further, this is the first report of Cellulomonas spp. coupling the oxidation of lactate, or other unknown electron donors in the absence of lactate, to the reduction of Cr(VI), Fe(III), and U(VI).

  4. Nitrate Enhanced Microbial Cr(VI) Reduction-Final Report

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    John F. Stolz

    2011-06-15

    A major challenge for the bioremediation of radionuclides (i.e., uranium, technetium) and metals (i.e., Cr(VI), Hg) is the co-occurrence of nitrate as it can inhibit metal transformation. Denitrification (nitrate reduction to dinitrogen gas) is considered the most important ecological process. For many metal and metalloid reducing bacteria, however, ammonia is the end product through respiratory nitrate reduction (RNRA). The focus of this work was to determine how RNRA impacts Cr(VI) transformation. The goal was to elucidate the specific mechanism(s) that limits Cr(VI) reduction in the presence of nitrate and to use this information to develop strategies that enhance Cr(VI) reduction (and thus detoxification). Our central hypothesis is that nitrate impacts the biotransformation of metals and metalloids in three ways 1) as a competitive alternative electron acceptor (inhibiting transformation), 2) as a co-metabolite (i.e., concomitant reduction, stimulating transformation), and 3) as an inducer of specific proteins and pathways involved in oxidation/reduction reactions (stimulating transformation). We have identified three model organisms, Geobacter metallireducens (mechanism 1), Sulfurospirillum barnesii, (mechasism 2), and Desulfovibrio desulfuricans (mechanisms 3). Our specific aims were to 1) investigate the role of Cr(VI) concentration on the kinetics of both growth and reduction of nitrate, nitrite, and Cr(VI) in these three organisms; 2) develop a profile of bacterial enzymes involved in nitrate transformation (e.g., oxidoreductases) using a proteomic approach; 3) investigate the function of periplasmic nitrite reductase (Nrf) as a chromate reductase; and 4) develop a strategy to maximize microbial chromium reduction in the presence of nitrate. We found that growth on nitrate by G. metallireducens was inhibited by Cr(VI). Over 240 proteins were identified by LC/MS-MS. Redox active proteins, outer membrane heavy metal efflux proteins, and chemotaxis sensory

  5. Investigations on photoelectrocatalytic reduction of Cr(VI) over titanium dioxide anode and metal cathode

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    Song, Han; Shang, Jing, E-mail: shangjing@pku.edu.cn; Ye, Junhui; Li, Qian

    2014-01-31

    Photocatalytic and photoelectrocatalytic (PEC) reductions of Cr(VI) based on TiO{sub 2} thin films were investigated under various conditions. Photogenerated electrons transferred from TiO{sub 2} thin film to cathode can contribute to PEC reduction of Cr(VI) only when the Fermi level of cathode lies above the chemical potential of Cr(VI), almost independent on the applied voltage of the direct current. In addition, the TiO{sub 2}-coated anode is the major site that accommodates the PEC reduction of Cr(VI) with hole scavenger citric acid, regardless of the Fermi level of the cathode. Although electron transfer from TiO{sub 2} to Cr(VI) is an exothermic process, the photogenerated holes in TiO{sub 2} can markedly hamper Cr(VI) reduction over the TiO{sub 2} thin film by oxidizing the lower-valence Cr back to Cr(VI), which may be counteracted by the citric acid. This research provides some in-depth insights on developing photocatalysts which enable highly efficient PEC reduction of Cr(VI) in the future. - Highlights: • Cr(VI) reduction on TiO{sub 2} photoanode is dominant with the addition of citric acid. • Cr(VI) is reduced on photocathode with Fermi level above Cr(VI) chemical potential. • Photogenerated holes can hamper Cr(VI) photoreduction over TiO{sub 2}.

  6. Cr(VI) reduction by Bacillus coagulans isolated from contaminated soils

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    Philip, L.; Iyengar, L. [Indian Inst. of Tech., Kharagpur (India); Venkobachar, C. [Univ. of West Indies, St. Augustine (Trinidad and Tobago). Dept. of Civil Engineering

    1998-12-01

    Investigation on Cr(VI) reduction was conducted using bacteria isolated from soil samples receiving electroplating wastewater. Chromium reduction capacity of these isolates was compared with that of Pseudomonas aeruginosa, a pure culture procured from the Institute of Microbial Technology, as well as Bacillus circulans, a laboratory isolate from garden soil. Bacillus coagulans, isolated and identified from chromium polluted soil, gave maximum reduction potential among all organisms studied. Malate was found to yield maximum biotransformation out of four electron donors employed. B. coagulans was able to reduce Cr(VI) even at 10 mM initial Cr(VI) concentration. With an increase in initial cell density, Cr(VI) reduction capacity was also increased; however, maximum specific biotransformation occurred at low cell densities. The optimum pH for Cr(VI) reduction was 7. Sulphates and nitrates did not compete with Cr(VI) for accepting the electrons. The presence of respiratory inhibitors like DNP and NaN{sub 3} marginally reduced the Cr(VI) reduction capacity. Cell free extracts were able to reduce Cr(VI) even in the absence of external electron donors; however, marginal increase was found in the presence of malate, nicotinamide adenine dinucleotide, and reduced nicotinamide adenine dinucleotide. The contribution of cell membrane in Cr(VI) reduction was negligible. Hence, the soluble enzymes appear to be responsible for Cr(VI) reduction by B. coagulans.

  7. An ecological new approach for treating Cr(VI)-containing industrial wastewater: Photochemical reduction.

    Science.gov (United States)

    Liu, Jie; Huang, Kun; Xie, Keng; Yang, Ying; Liu, Huizhou

    2016-04-15

    An ecological new approach for photochemical reduction of Cr(VI) in aqueous solution by adding into water-soluble copolymer, polyethylene glycol (PEG), was investigated. Various influences including light intensity, initial solution pH value, PEG molecular weight and initial concentration ratio of PEG to Cr(VI) on photochemical reduction of Cr(VI) were discussed, and a possible reaction mechanism was proposed. Experimental results revealed that Cr(VI) could be reduced to Cr(III) by PEG under sunlight irradiation. The photo-reduction rate of Cr(VI) increased with the decrease of solution pH and PEG molecular weight, but increased with the light intensity. The reduction percentage of Cr(VI) increased with the initial concentration ratio of PEG to Cr(VI). When the initial solution pH value was below 3.0, almost all of Cr(VI) was completely reduced to Cr(III) within 20 min of 50 × 10(3) lux solar irradiation in the presence of PEG. After photo-reduction, PEG and Cr(III) in aqueous solutions could be recovered by adding into a high-concentrated Na2SO4 aqueous solution to induce the formation of a stable PEG-based aqueous biphasic system. By doing so, Na2SO4 in aqueous solution could also be removed. The present work highlights a promising new route for treating the industrial wastewater containing toxic Cr(VI) ions by adding into environmental-friendly PEG for photo-reduction of Cr(VI) to Cr(III), and then salting-out recovery of PEG and removal of Cr(III) in wastewater by adding into another high-salt wastewater, so that the high-salt wastewater could also be treated. Copyright © 2016 Elsevier Ltd. All rights reserved.

  8. Reduction of Cr(VI) to Cr(III) by wetland plants: Potential for in situ heavy metal detoxification

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    Lytle, C.M.; Qian, J.H.; Hansen, D.; Zayed, A.; Terry, N. [Univ. of California, Berkeley, CA (United States). Dept. of Plant and Microbial Biology; Lytle, F.W. [The EXAFS Co., Pioche, NV (United States); Yang, N. [Sandia National Labs., Livermore, CA (United States)

    1998-10-15

    Reduction of heavy metals in situ by plants may be a useful detoxification mechanism for phytoremediation. Using X-ray spectroscopy, the authors show that Eichhornia crassipes (water hyacinth), supplied with Cr(VI) in nutrient culture, accumulated nontoxic Cr(III) in root and shoot tissues. The reduction of Cr(VI) to Cr(III) appeared to occur in the fine lateral roots. The Cr(III) was subsequently translocated to leaf tissues. Extended X-ray absorption fine structure of Cr in leaf and petiole differed when compared to Cr in roots. In roots, Cr(III) was hydrated by water, but in petiole and more so in leaf, a portion of the Cr(III) may be bound to oxalate ligands. This suggests that E. crassipes detoxified Cr(VI) upon root uptake and transported a portion of the detoxified Cr to leaf tissues. Cr-rich crystalline structures were observed on the leaf surface. The chemical species of Cr in other plants, collected from wetlands that contained Cr(VI)-contaminated wastewater, was also found to be Cr(III). The authors propose that this plant-based reduction of Cr(VI) by E. crassipes has the potential to be used for the in situ detoxification of Cr(VI)-contaminated wastestreams.

  9. Visible light Cr(VI) reduction and organic chemical oxidation by TiO2 photocatalysis.

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    Sun, Bo; Reddy, Ettireddy P; Smirniotis, Panagiotis G

    2005-08-15

    Here we report the simultaneous Cr(VI) reduction and 4-chlorophenol (4-CP) oxidation in water under visible light (wavelength > 400 nm) using commercial Degussa P25 TiO2. This remarkable observation was attributed to a synergistic effect among TiO2, Cr(VI), and 4-CP. It is well known that TiO2 alone cannot remove either 4-CP or Cr(VI) efficiently under visible light. Moreover, the interaction between Cr(VI) and 4-CP is minimal if not negligible. However, we found that the combination of TiO2, Cr(VI), and 4-CP together can enable efficient Cr(VI) reduction and 4-CP oxidation under visible light. The specific roles of the three ingredients in the synergistic system were studied parametrically. It was found that optimal concentrations of Cr(VI) and TiO2 exist for the Cr(VI) reduction and 4-CP oxidation. Cr(VI) was compared experimentally with other metals such as Cu(ll), Fe(lll), Mn(IV), Ce(IV), and V(V). Among all these metal ions, only Cr(VI) promotes the photocatalytic oxidation of 4-CP. The amount of 4-CP removed was directly related to the initial concentration of Cr(VI). The system was also tested with four other chemicals (aniline, salicylic acid, formic acid, and diethyl phosphoramidate). We found that the same phenomenon occurred for organics containing acid and/or phenolic groups. Cr(VI) was reduced at the same time as the organic chemicals being oxidized during photoreaction under visible light. The synergistic effect was also found with pure anatase TiO2 and rutile TiO2. This study demonstrates a possible economical way for environmental cleanup under visible light.

  10. Isotope fractionation and spectroscopic analysis as an evidence of Cr(VI) reduction during biosorption.

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    Šillerová, Hana; Chrastný, Vladislav; Čadková, Eva; Komárek, Michael

    2014-01-01

    This work investigates the mechanisms behind Cr(VI) biosorption/reduction on three biomaterials (brewers draff, grape waste and synthetic humic acid). Coupled Cr isotope analysis with ICP-OES, XPS and SEM was tested as a novel approach to study the reduction of Cr(VI) by the biomaterials. The Cr(VI) biosorption process was accompanied with heavier Cr isotopes enrichment in the remaining Cr(VI) fraction. A significant fractionation of Cr stable isotopes was observed with no significant pH effect; δ(53)Cr of the remaining fraction ranged from 0.2‰ to 1.9‰ while δ(53)Cr of the product (sorbed Cr) ranged from -1.2‰ to -2.8‰. The Rayleigh fractionation model fitted well the measured data and Cr isotope analysis provides thus an efficient tool to quantify Cr(VI) reduction by different biomaterials. In general, the sorption/reduction potential of the three studied biomaterials decreased in the following order: grape waste>humic acids>brewers draff. Copyright © 2013 Elsevier Ltd. All rights reserved.

  11. Cr(VI) reduction at rutile-catalyzed cathode in microbial fuel cells

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    Li, Yan; Lu, Anhuai; Ding, Hongrui; Yan, Yunhua; Wang, Changqiu; Zen, Cuiping; Wang, Xin [The Key Laboratory of Orogenic Belts and Crustal Evolution, School of Earth and Space Sciences, Peking University, Beijing 100871 (China); Jin, Song [MWH Americas, 3665 JFK Parkway, Suite 206, Fort Collins, CO 80525 (United States); Department of Civil and Architectural Engineering, University of Wyoming, Laramie, WY 82071 (United States)

    2009-07-15

    Cathodic reduction of hexavalent chromium (Cr(VI)) and simultaneous power generation were successfully achieved in a microbial fuel cell (MFC) containing a novel rutile-coated cathode. The selected rutile was previously characterized to be sensitive to visible light and capable of both non-photo- and photocatalysis. In the MFCs containing rutile-coated cathode, Cr(VI) was rapidly reduced in the cathode chamber in presence and absence of light irradiation; and the rate of Cr(VI) reduction under light irradiation was substantially higher than that in the dark. Under light irradiation, 97% of Cr(VI) (initial concentration 26 mg/L) was reduced within 26 h, which was 1.6 x faster than that in the dark controls in which only background non-photocatalysis occurred. The maximal potential generated under light irradiation was 0.80 vs. 0.55 V in the dark controls. These results indicate that photocatalysis at the rutile-coated cathode in the MFCs might have lowered the cathodic overpotential, and enhanced electron transfer from the cathode to Cr(VI) for its reduction. In addition, photoexcited electrons generated during the cathode photocatalysis might also have contributed to the higher Cr(VI) reduction rates when under light irradiation. This work assessed natural rutile as a novel cathodic catalyst for MFCs in power generation; particularly it extended the practical merits of conventional MFCs to cathodic reduction of environmental contaminants such as Cr(VI). (author)

  12. Photocatalytic reduction of Cr(VI) by citric and oxalic acids over biogenetic jarosite.

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    Xu, Zhihui; Bai, Shuangyou; Liang, Jianru; Zhou, Lixiang; Lan, Yeqing

    2013-05-01

    In this study, a series of bath experiments were carried out to investigate the photoreduction of Cr(VI) by small molecular weight organic acids (SOAs) over jarosite, a mineral found in acid mine drainage (AMD). The results demonstrated that jarosite or SOAs alone was unable to effectively transform Cr(VI) to Cr(III) even if exposed to an illumination of mimic solar light. However, an addition of jarosite significantly enhanced the reduction of Cr(VI) by SOAs under the same condition. The photocatalytic reduction of Cr(VI) was strongly influenced by pH, the initial concentrations and the structures of SOAs. Of the tested two SOAs, the reaction rates of photocatalytic reduction of Cr(VI) were in the order of oxalic acid>citric acid. The reaction obeyed to zero-order kinetics with respect to Cr(VI) with excess SOAs. A possible mechanism for photoreduction of Cr(VI) by SOAs over jarosite was proposed. Copyright © 2013 Elsevier B.V. All rights reserved.

  13. Photocatalytic reduction of Cr(VI) by small molecular weight organic acids over schwertmannite.

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    Jiang, Danjun; Li, Ying; Wu, Yong; Zhou, Pei; Lan, Yeqing; Zhou, Lixiang

    2012-10-01

    In this study, a series of bath experiments was carried out to investigate the photoreduction of Cr(VI) by small molecular weight organic acids (SOAs) over schwertmannite, a mineral found in acid mine drainage (AMD). The results demonstrated that schwertmannite or SOAs alone was unable to effectively transform Cr(VI) to Cr(III) even if exposed to an illumination of mimic solar light. However, an addition of schwertmannite significantly enhanced the reduction of Cr(VI) by SOAs under the same condition. For example, 100μM Cr(VI) was almost completely removed within 50min in the presence of both schwertmannite (0.6gL(-1)) and oxalic acid (300μM) at pH 3.0. The photocatalytic reduction of Cr(VI) was strongly influenced by pH, the initial concentrations and the structures of SOAs. Of the tested three SOAs, the reaction rates of photocatalytic reduction of Cr(VI) were in the order of oxalic acid>citric acid>tartaric acid. The reaction obeyed to zero-order kinetics with respect to Cr(VI) with excess SOAs. A possible mechanism for photoreduction of Cr(VI) by SOAs over schwertmannite was proposed. Fe(III) on the surface of schwertmannite was dissolved by SOAs, and then Fe(III)-SOA complexes with high photochemical activity formed. Further, Fe(II) together with organic acid radicals, CO(2)(-) and O(2)(-), was generated through a metal-ligand-charge-transfer pathway (MLCT), leading to a rapid reduction of Cr(VI). Copyright © 2012 Elsevier Ltd. All rights reserved.

  14. Reduction of Cr(VI) to Cr(III) using silicon nanowire arrays under visible light irradiation.

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    Fellahi, Ouarda; Barras, Alexandre; Pan, Guo-Hui; Coffinier, Yannick; Hadjersi, Toufik; Maamache, Mustapha; Szunerits, Sabine; Boukherroub, Rabah

    2016-03-05

    We report an efficient visible light-induced reduction of hexavalent chromium Cr(VI) to trivalent Cr(III) by direct illumination of an aqueous solution of potassium dichromate (K2Cr2O7) in the presence of hydrogenated silicon nanowires (H-SiNWs) or silicon nanowires decorated with copper nanoparticles (Cu NPs-SiNWs) as photocatalyst. The SiNW arrays investigated in this study were prepared by chemical etching of crystalline silicon in HF/AgNO3 aqueous solution. The Cu NPs were deposited on SiNW arrays via electroless deposition technique. Visible light irradiation of an aqueous solution of K2Cr2O7 (10(-4)M) in presence of H-SiNWs showed that these substrates were not efficient for Cr(VI) reduction. The reduction efficiency achieved was less than 10% after 120 min irradiation at λ>420 nm. Addition of organic acids such as citric or adipic acid in the solution accelerated Cr(VI) reduction in a concentration-dependent manner. Interestingly, Cu NPs-SiNWs was found to be a very efficient interface for the reduction of Cr(VI) to Cr(III) in absence of organic acids. Almost a full reduction of Cr(VI) was achieved by direct visible light irradiation for 140 min using this photocatalyst. Copyright © 2015 Elsevier B.V. All rights reserved.

  15. Reduction of Cr(VI) to Cr(III) using silicon nanowire arrays under visible light irradiation

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    Fellahi, Ouarda [Institut d' Electronique, de Microélectronique et de Nanotechnologie (IEMN), UMR CNRS 8520, Avenue Poincaré—BP 70478, 59652 Villeneuve d' Ascq Cedex (France); Centre de Recherche en Technologie des Semi-conducteurs pour l' Energétique-CRTSE 02, Bd Frantz Fanon, BP. 140, Alger 7 Merveilles (Algeria); Barras, Alexandre [Institut d' Electronique, de Microélectronique et de Nanotechnologie (IEMN), UMR CNRS 8520, Avenue Poincaré—BP 70478, 59652 Villeneuve d' Ascq Cedex (France); Pan, Guo-Hui [State Key Laboratory of Luminescence and Applications, Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, 3888 Dong Nanhu Road, Changchun 130033 (China); Coffinier, Yannick [Institut d' Electronique, de Microélectronique et de Nanotechnologie (IEMN), UMR CNRS 8520, Avenue Poincaré—BP 70478, 59652 Villeneuve d' Ascq Cedex (France); Hadjersi, Toufik [Centre de Recherche en Technologie des Semi-conducteurs pour l' Energétique-CRTSE 02, Bd Frantz Fanon, BP. 140, Alger 7 Merveilles (Algeria); Maamache, Mustapha [Laboratoire de Physique Quantique et Systèmes Dynamiques, Département de Physique, Université de Sétif, Sétif 19000 (Algeria); Szunerits, Sabine [Institut d' Electronique, de Microélectronique et de Nanotechnologie (IEMN), UMR CNRS 8520, Avenue Poincaré—BP 70478, 59652 Villeneuve d' Ascq Cedex (France); and others

    2016-03-05

    Highlights: • Cr(VI) reduction to Cr(III) using silicon nanowires decorated with Cu nanoparticles. • The reduction takes place at room temperature and neutral pH under visible light. • The photocatalytic reduction was enhanced by addition of adipic or citric acid. - Abstract: We report an efficient visible light-induced reduction of hexavalent chromium Cr(VI) to trivalent Cr(III) by direct illumination of an aqueous solution of potassium dichromate (K{sub 2}Cr{sub 2}O{sub 7}) in the presence of hydrogenated silicon nanowires (H-SiNWs) or silicon nanowires decorated with copper nanoparticles (Cu NPs-SiNWs) as photocatalyst. The SiNW arrays investigated in this study were prepared by chemical etching of crystalline silicon in HF/AgNO{sub 3} aqueous solution. The Cu NPs were deposited on SiNW arrays via electroless deposition technique. Visible light irradiation of an aqueous solution of K{sub 2}Cr{sub 2}O{sub 7} (10{sup −4} M) in presence of H-SiNWs showed that these substrates were not efficient for Cr(VI) reduction. The reduction efficiency achieved was less than 10% after 120 min irradiation at λ > 420 nm. Addition of organic acids such as citric or adipic acid in the solution accelerated Cr(VI) reduction in a concentration-dependent manner. Interestingly, Cu NPs-SiNWs was found to be a very efficient interface for the reduction of Cr(VI) to Cr(III) in absence of organic acids. Almost a full reduction of Cr(VI) was achieved by direct visible light irradiation for 140 min using this photocatalyst.

  16. Reactive transport modeling of chromium isotope fractionation during Cr(VI) reduction.

    Science.gov (United States)

    Jamieson-Hanes, Julia H; Amos, Richard T; Blowes, David W

    2012-12-18

    Chromium isotope fractionation is indicative of mass-transfer processes, such as reduction of Cr(VI) to Cr(III) during groundwater remediation. Laboratory experiments comparing batch and column treatment of Cr(VI) using organic carbon suggest that the associated isotope fractionation may be influenced by solute-transport mechanisms. These batch and column experiments were simulated using the reactive transport model MIN3P to further evaluate the effects of Cr reduction and transport on isotope fractionation under saturated flow conditions. Simulation of the batch experiment provided a good fit to the experimental data, where a fractionation factor (α₅₃) of 0.9965 was attributed to a single, dominant Cr(VI) removal mechanism. Calibration of the column simulations to the experimental results suggested the presence of a second, more rapid Cr(VI) removal mechanism with α₅₃ = 0.9992. Results from this study demonstrate that the interpretation of Cr isotope fractionation during reduction can be complex, particularly where multiple removal mechanisms are evident. Reactive transport modeling of Cr isotope fractionation can provide a quantitative assessment of the contaminant removal mechanisms, thus improving the application of Cr isotope measurements as a tool to track Cr(VI) migration and attenuation in groundwater.

  17. Reduction and removal of Cr(VI) from aqueous solutions using modified byproducts of beer production.

    Science.gov (United States)

    Cui, Haojie; Fu, Minglai; Yu, Shen; Wang, Ming Kuang

    2011-02-28

    Biosorption, as an effective and low-cost technology treating industrial wastewaters containing Cr(VI), has become a significant concern worldwide. In this work, acid-modified byproducts of beer production (BBP) were used to remove Cr(VI) from aqueous solutions. Removal of Cr(VI) increases as the pH is decreased from 4.0 to 1.5, but the maximum of total Cr removal is obtained in a pH range from 2.0 to 2.5. Nearly 60% of the initial Cr(VI) (100 mg L(-1)) was adsorbed or reduced to Cr(III) within the first 10 min at pH 2.0. The Cr(VI) removal capability of acid-modified BBP materials was almost completely retained after regenerating with acid. FT-IR and XPS spectra revealed that carboxylate and carboxyl groups on the surface of modified BBP materials play a major role in Cr(VI) binding and reduction, whereas amide and other groups play a minor role in the Cr(VI) removal process. Copyright © 2010 Elsevier B.V. All rights reserved.

  18. Effect of thiols enrichment on Cr(VI) photo-reduction by natural organic matter (NOM).

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    Luo, Hong-Wei

    2016-05-01

    Photochemical redox transformation of Cr(VI)-NOM complexes substantially affects transport and speciation of less toxic Cr(III) in natural waters. However, the underlying mechanisms remain unclear. This study reported photochemical reactions of Cr(VI) with thiol-enriched NOM under acidic condition. More effective thiols enrichment in humic acid (HA) was observed than that in fulvic acid (FA), thereby resulting in a higher reduction capacity and faster rate of Cr(VI) photo-reduction. Chemical addition of sulfide to HA formed a large number of S-containing molecular formulae, which subsequently disappeared following reactions with Cr(VI) under solar irradiation. Cr(VI) photo-reduction in thiol-enriched HA consumed more S-containing formulae. Solar irradiation caused a rapid loss of the reduction capacities and thiol contents in HA and FA. All these findings can provide useful information for understanding the biogeochemical cycles of chromium and sulfur, and are also of environmental significance because they may partially account for photo-transformation of Cr(VI) when chromium enters into the aquatic environment as acidic industrial effluents. Copyright © 2016 Elsevier Ltd. All rights reserved.

  19. Reduction of toxic Cr(VI)-humic acid in an ionic liquid

    Science.gov (United States)

    Huang, Hsin-Liang; Huang, Hsin-Hung; Wei, Yu Jhe

    2017-07-01

    Remediation of soil contaminated by toxic hexavalent chromium species associated with humic acid (Cr(VI)-HA) and absorbed Cr(VI) in pores frequently experiences technical difficulties. In the present work, a feasibility study for extraction of the Cr(VI) species from a molecular sieve MCM-41 (Mobil Composition of Matter No. 41) that was used to simulate the pore system of soil, with a green solvent (ionic liquid), 1-butyl-3-methylimidazolium chloride ([C4mim][Cl]), was carried out. After a 30-min extraction, approximately 70% of the Cr(VI) species can be extracted. By component fitted X-ray absorption near edge structure (XANES) spectroscopy, about 48% of the Cr(VI)-HA are reduced to form less toxic species (Cr(III)-HA) during extraction with [C4mim][Cl]. Note that the Cr-O in the [C4mim][Cl] phase has a slightly greater bond distance (BD) (0.162 nm) possibly due to the fact of that the fraction of Cr(III) is increased in the extraction process. The non-extractable chromium remaining in MCM-41 has a much greater fraction of Cr(III) (78%) and its BD is further increased to 0.195 nm. The coordination numbers of chromium for the 1st shell Cr-O in the Cr(VI) and Cr(III) species are in the range of 2.4-2.9, suggesting that chromium is chelated with HA and adsorbed in MCM-41. The 1H NMR data also suggest that the enhanced reduction of the Cr(VI) species may be related to interactions between chromium species and electron-rich imidazole ring of the [C4mim]+. This work also exemplifies that the fate of toxic chromium species in the complicated remediation of contaminated soils can be revealed in a molecule-scale study by synchrotron X-ray absorption spectroscopy.

  20. Characterization of Product and Potential Mechanism of Cr(VI) Reduction by Anaerobic Activated Sludge in a Sequencing Batch Reactor.

    Science.gov (United States)

    Jin, Ruofei; Liu, Yao; Liu, Guangfei; Tian, Tian; Qiao, Sen; Zhou, Jiti

    2017-05-10

    Bioremediation of Cr(VI) and nitrate is considered as a promising and cost-effective alternative to chemical and physical methods. However, organo-Cr(III) complexes in effluent generally causes environmental concerns due to second-pollution. Here, Cr(VI) reduction and immobilization efficiencies of anaerobic activated sludge were investigated. Anaerobic activated sludge showed strong reduction ability of Cr(VI) and possessed a great potential of Cr(III) immobilization. Almost 100.0 mg l(-1) Cr(VI) could be completely reduced and immobilized by anaerobic activated sludge in a sequencing batch reactor in 24 h. And most generated Cr(III) was accumulated outside of sludge cells. Extracellular polymeric substances (EPS) could bind to Cr(VI) and form EPS-Cr(VI) interaction to reduce the toxic effect of Cr(VI) and promote the Cr(VI) reduction. Protein-like and humic-like substances were responsible for binding with Cr(VI), meanwhile the process was a thermodynamically favorable binding reaction. Then Cr(VI) was reduced to Cr(III) by membrane-associated chromate reductase of sludge. Eventually, the generated Cr(III) might exist as poly-nuclear Cr(III) complexes adhered to sludge surfaces.

  1. A simple Cr(VI)–S(IV)–O{sub 2} system for rapid and simultaneous reduction of Cr(VI) and oxidative degradation of organic pollutants

    Energy Technology Data Exchange (ETDEWEB)

    Yuan, Yanan; Yang, Shaojie [Department of Environmental Science, Hubei Key Lab of Biomass Resource Chemistry and Environmental Biotechnology, School of Resources and Environmental Science, Wuhan University, 430079 (China); Zhou, Danna, E-mail: zdncug@163.com [Faculty of Material Science and Chemistry, China University of Geosciences, Wuhan 430074 (China); Wu, Feng [Department of Environmental Science, Hubei Key Lab of Biomass Resource Chemistry and Environmental Biotechnology, School of Resources and Environmental Science, Wuhan University, 430079 (China)

    2016-04-15

    Highlights: • Rapid and simultaneous reduction of Cr(VI) and degradation of organic pollutants occur. • Oxysulfur radicals generated in Cr(VI)–S(IV)–O{sub 2} system oxidize the organic pollutants. • Acidic pH facilitates the reactions from both directions of reduction and oxidation. • Degradation potential of aromatic amines depends on the substituted groups. • Cr(VI)–S(IV)–O{sub 2} system is promising for “waste control by waste”. - Abstract: Hexavalent chromium (Cr(VI)), a heavy-metal contaminant, can be easily reduced to less toxic trivalent chromium (Cr(III)) by sulfite ions (S(IV)). However, S(IV) has not drawn as much attention as the ferrous ion has. We report herein a novel Cr(VI)–S(IV)–O{sub 2} system containing sulfite ions that rapidly and simultaneously reduces Cr(VI) and oxidize organic pollutants in the presence of oxygen in aqueous solutions. This Cr(VI)–S(IV)-O{sub 2} system contains the initiator Cr(VI), the reductant S(IV), and the oxidant O{sub 2}, which produce oxysulfur radicals (mainly SO{sub 4}·{sup −} and SO{sub 5}·{sup −}) and hydroxyl radicals (OH·). The Cr(VI)/S(IV) molar ratio, pH, and oxygen content play important roles in the entire reaction system. Acidic conditions (pH 3.0) facilitated degradation of organic compounds and reduction of Cr(VI) as well. In addition, experiments of rapid degradation of several kinds of organic pollutants such as azo dye (acid orange 7, AO7), aniline, phenol, bisphenol A etc were also conducted. Preliminary results show that the removal rates of the analogs of phenols or aromatic amines in this Cr(VI)–S(IV)–O{sub 2} system have a relationship with the electronic parameters (Hammett constant, σ) of the substituted groups. Thus, the Cr(VI)–S(IV)–O{sub 2} system, provides an excellent strategy of “waste control by waste” for removing multiple industrial contaminants.

  2. Cr(VI) reduction in wastewater using a bimetallic galvanic reactor

    Energy Technology Data Exchange (ETDEWEB)

    Lugo-Lugo, Violeta [Centro Conjunto de Investigacion en Quimica Sustentable UAEM-UNAM, Universidad Autonoma del Estado de Mexico, Facultad de Quimica. Paseo Colon interseccion Paseo Tollocan S/N. C.P. 50120, Toluca (Mexico); Barrera-Diaz, Carlos, E-mail: cbarrera@uaemex.mx [Centro Conjunto de Investigacion en Quimica Sustentable UAEM-UNAM, Universidad Autonoma del Estado de Mexico, Facultad de Quimica. Paseo Colon interseccion Paseo Tollocan S/N. C.P. 50120, Toluca (Mexico); Bilyeu, Bryan [Xavier University of Louisiana, Department of Chemistry, 1 Drexel Drive, New Orleans, LA 70125 (United States); Balderas-Hernandez, Patricia [Centro Conjunto de Investigacion en Quimica Sustentable UAEM-UNAM, Universidad Autonoma del Estado de Mexico, Facultad de Quimica. Paseo Colon interseccion Paseo Tollocan S/N. C.P. 50120, Toluca (Mexico); Urena-Nunez, Fernando [Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, Col. Escandon, Delegacion Miguel Hidalgo, C.P. 11801, Mexico, D.F. (Mexico); Sanchez-Mendieta, Victor [Centro Conjunto de Investigacion en Quimica Sustentable UAEM-UNAM, Universidad Autonoma del Estado de Mexico, Facultad de Quimica. Paseo Colon interseccion Paseo Tollocan S/N. C.P. 50120, Toluca (Mexico)

    2010-04-15

    The electrochemical reduction of Cr(VI)-Cr(III) in wastewater by iron and copper-iron bimetallic plates was evaluated and optimized. Iron has been used as a reducing agent, but in this work a copper-iron galvanic system in the form of bimetallic plates is applied to reducing hexavalent chromium. The optimal pH (2) and ratio of copper to iron surface areas (3.5:1) were determined in batch studies, achieving a 100% reduction in about 25 min. The Cr(VI) reduction kinetics for the bimetallic system fit a first order mechanism with a correlation of 0.9935. Thermodynamic analysis shows that the Cr(VI) reduction is possible at any pH value. However, at pH values above 3.0 for iron and 5.5 for chromium insoluble species appear, indicating that the reaction will be hindered. Continuous column studies indicate that the bimetallic copper-iron galvanic system has a reduction capacity of 9.5890 mg Cr(VI) cm{sup -2} iron, whereas iron alone only has a capacity of 0.1269 mg Cr(VI) cm{sup -2}. The bimetallic copper-iron galvanic system is much more effective in reducing hexavalent chromium than iron alone. The exhausted plates were analyzed by SEM, EDS, and XRD to determine the mechanism and the surface effects, especially surface fouling.

  3. Solid state reduction of chromium (VI) pollution for Al2O3-Cr metal ceramics application

    Science.gov (United States)

    Zhu, Hekai; Fang, Minghao; Huang, Zhaohui; Liu, Yangai; Tang, Hao; Min, Xin; Wu, Xiaowen

    2016-04-01

    Reduction of chromium (VI) from Na2CrO4 through aluminothermic reaction and fabrication of metal-ceramic materials from the reduction products have been investigated in this study. Na2CrO4 could be successfully reduced into micrometer-sized Cr particles in a flowing Ar atmosphere in presence of Al powder. The conversion ratio of Na2CrO4 to metallic Cr attained 96.16% efficiency. Al2O3-Cr metal-ceramic with different Cr content (5 wt%, 10 wt%, 15 wt%, 20 wt%) were further prepared from the reduction product Al2O3-Cr composite powder, and aluminum oxide nanopowder via pressure-less sintering. The phase composition, microstructure and mechanical properties of metal-ceramic composites were characterized to ensure the potential of the Al2O3-Cr composite powder to form ceramic materials. The highest relative density and bending strength can reach 93.4% and 205 MP, respectively. The results indicated that aluminothermic reduction of chromium (VI) for metal-ceramics application is a potential approach to remove chromium (VI) pollutant from the environment.

  4. Reduction process of Cr(VI) by Fe(II) and humic acid analyzed using high time resolution XAFS analysis.

    Science.gov (United States)

    Hori, Mayumi; Shozugawa, Katsumi; Matsuo, Motoyuki

    2015-03-21

    The initial reduction behavior of Cr(VI) to Cr(III) has not been clearly understood due to its rapid reduction reaction. In order to study the reduction process of Cr(VI) in detail, we applied quick X-ray absorption fine structure (QXAFS) analysis to observe how Cr(VI) was reduced to Cr(III) by Fe(II) and humic acid (HA) with time. The Cr(VI) concentration was analyzed every 60s, and the plots of ln(Cr(VI)/Cr(VI)0) versus time were used to evaluate the reduction process based on their linearity. Reduction by Fe(II) showed a linear relation, whereas reduction by HA showed a nonlinear relation. With combined Fe(II) and HA, the linearity was unlike those of Fe(II) and HA individually. The reduction rate was not constant. The structure of Fe(II) produced by HA during the Cr(VI) reduction was investigated by using Mössbauer spectroscopy, which showed that Fe(II) produced by HA reduction of Fe(III) had the same structure as the initial Fe(II). HA can reduce Fe(III) back to Fe(II), and reproduced Fe(II) reduces Cr(VI). For Cr(VI) reduction by combined Fe(II) and HA, each reductant contribute differently: Fe(II) directly contributes to the Cr(VI) reaction, whereas HA reduces both Cr(VI) and Fe(III). Copyright © 2014 Elsevier B.V. All rights reserved.

  5. Isolation and characterization of Cr(VI) reducing Cellulomonas spp. from subsurface soils: Implications for long-term chromate reduction

    Energy Technology Data Exchange (ETDEWEB)

    S. Viamajala; W. Smith; R. Sani; W. Apel; J. Petersen; A. Neal; F. Roberto; D. Newby; B. Peyton

    2007-02-01

    Microbial enrichments from Cr(VI) contaminated and uncontaminated US Department of Energy Hanford Site sediments produced Cr(VI) reducing consortia when grown in the presence of Cr(VI) with acetate, D-xylose or glycerol as a carbon and energy source. Eight of the nine isolates from the consortia were Gram positive and four of these were identified by 16S rRNA sequence homology and membrane fatty acid composition as belonging to the genus Cellulomonas. Two strains, ES6 and WS01, were further examined for their ability to reduce Cr(VI) under growth and non-growth conditions. During fermentative growth on D-xylose, ES6 and WS01 decreased aqueous Cr(VI) concentrations from 0.04 mM Cr(VI) to below the detection limit (0.002 mM Cr(VI)) in less than three days and retained their ability to reduce Cr(VI) even after four months of incubation. Washed ES6 and WS01 cells also reduced Cr(VI) under non-growth conditions for over four months, both with and without the presence of an exogenous electron donor. K-edge XANES spectroscopy confirmed the reduction of Cr(VI) to Cr(III). The ability to reduce Cr(VI) after growth had stopped and in the absence of an external electron donor, suggests that stimulation of these types of organisms may lead to effective long-term, in situ passive reactive barriers for Cr(VI) removal. Our results indicate that Cr(VI) reduction by indigenous Cellulomonas spp. may be a potential method of in situ bioremediation of Cr(VI) contaminated sediment and groundwater.

  6. Isolation and characterization of Cr(VI) reducing Cellulomonas spp. from subsurface soils: implications for long-term chromate reduction.

    Science.gov (United States)

    Viamajala, Sridhar; Smith, William A; Sani, Rajesh K; Apel, William A; Petersen, James N; Neal, Andrew L; Roberto, F F; Newby, D T; Peyton, Brent M

    2007-02-01

    Microbial enrichments from Cr(VI) contaminated and uncontaminated US Department of Energy Hanford Site sediments produced Cr(VI) reducing consortia when grown in the presence of Cr(VI) with acetate, D-xylose or glycerol as a carbon and energy source. Eight of the nine isolates from the consortia were Gram positive and four of these were identified by 16S rRNA sequence homology and membrane fatty acid composition as belonging to the genus Cellulomonas. Two strains, ES6 and WS01, were further examined for their ability to reduce Cr(VI) under growth and non-growth conditions. During fermentative growth on D-xylose, ES6 and WS01 decreased aqueous Cr(VI) concentrations from 0.04 mM Cr(VI) to below the detection limit (0.002 mM Cr(VI)) in less than three days and retained their ability to reduce Cr(VI) even after four months of incubation. Washed ES6 and WS01 cells also reduced Cr(VI) under non-growth conditions for over four months, both with and without the presence of an exogenous electron donor. K-edge XANES spectroscopy confirmed the reduction of Cr(VI) to Cr(III). The ability to reduce Cr(VI) after growth had stopped and in the absence of an external electron donor, suggests that stimulation of these types of organisms may lead to effective long-term, in situ passive reactive barriers for Cr(VI) removal. Our results indicate that Cr(VI) reduction by indigenous Cellulomonas spp. may be a potential method of in situ bioremediation of Cr(VI) contaminated sediment and groundwater.

  7. Photocatalytic Reduction of Aqueous Cr(VI) with CdS under Visible Light Irradiation: Effect of Particle Size

    OpenAIRE

    A. B. Makama; Ali Salmiaton; Elias B. Saion; T. S.Y. Choong; Abdullah, N.

    2017-01-01

    Stringent environmental standards have made the removal of Cr(VI) from water an important problem for environmental scientist and engineering. Heterogeneous photocatalysis using suspended photocatalyst is an interesting technique to consider for this application. In this work, the influence of particle size of suspended CdS on the photocatalytic reduction of aqueous Cr(VI) ion was investigated. The efficiency of Cr(VI) reduction was monitored through UV-visible analysis. The experimental resu...

  8. Flow-through Column Experiments and Modeling of Microbially Mediated Cr(VI) Reduction at Hanford 100H

    Science.gov (United States)

    Yang, L.; Molins, S.; Beller, H. R.; Brodie, E. L.; Steefel, C.; Nico, P. S.; Han, R.

    2010-12-01

    Microbially mediated Cr(VI) reduction at the Hanford 100H area was investigated by flow-through column experiments. Three separate experiments were conducted to promote microbial activities associated with denitrification, iron and sulfate reduction, respectively. Replicate columns packed with natural sediments from the site under anaerobic environment were injected with 5mM Lactate as the electron donor and 5 μM Cr(VI) in all experiments. Sulfate and nitrate solutions were added to act as the main electron acceptors in the respective experiments, while iron columns relied on the indigenous sediment iron (and manganese) oxides as electron acceptors. Column effluent solutions were analyzed by IC and ICP-MS to monitor the microbial consumption/conversion of lactate and the associated Cr(VI) reduction. Biogeochemical reactive transport modeling was performed to gain further insights into the reaction mechanisms and Cr(VI) bioreduction rates. All experimental columns showed a reduction of the injected Cr(VI). Columns under denitrifying conditions showed the least Cr(VI) reduction at early stages (adverse effect on Cr(VI) reduction rates. Reactive transport simulations indicated that biomass growth completely depleted influent ammonium, and called for an additional source of N to account for the measured reduction rates. Iron columns were the least active with undetectable consumption of the injected lactate, slowest cell growth, and the smallest change in Cr(VI) concentrations during the course of the experiment. In contrast, columns under sulfate-reducing/fermentative conditions exhibited the greatest Cr(VI) reduction capacity. Two sulfate columns evolved to complete lactate fermentation with acetate and propionate produced in the column effluent after 40 days of experiments. These fermenting columns showed a complete removal of injected Cr(VI), visible precipitation of sulfide minerals, and a significant increase in effluent Fe and Mn concentrations. Reactive

  9. Cr(Vi) reduction capacity of activated sludge as affected by nitrogen and carbon sources, microbial acclimation and cell multiplication

    Energy Technology Data Exchange (ETDEWEB)

    Ferro Orozco, A.M., E-mail: mferro@cidca.org.ar [Centro de Investigacion y Desarrollo en Criotecnologia de Alimentos (CIDCA) CCT La Plata CONICET - Fac. de Cs. Exactas, UNLP. 47 y 116 (B1900AJJ) La Plata (Argentina); Contreras, E.M.; Zaritzky, N.E. [Centro de Investigacion y Desarrollo en Criotecnologia de Alimentos (CIDCA) CCT La Plata CONICET - Fac. de Cs. Exactas, UNLP. 47 y 116 (B1900AJJ) La Plata (Argentina); Fac. de Ingenieria, UNLP. 47 y 1 (B1900AJJ) - La Plata (Argentina)

    2010-04-15

    The objectives of the present work were: (i) to analyze the capacity of activated sludge to reduce hexavalent chromium using different carbon sources as electron donors in batch reactors, (ii) to determine the relationship between biomass growth and the amount of Cr(VI) reduced considering the effect of the nitrogen to carbon source ratio, and (iii) to determine the effect of the Cr(VI) acclimation stage on the performance of the biological chromium reduction assessing the stability of the Cr(VI) reduction capacity of the activated sludge. The highest specific Cr(VI) removal rate (q{sub Cr}) was attained with cheese whey or lactose as electron donors decreasing in the following order: cheese whey {approx} lactose > glucose > citrate > acetate. Batch assays with different nitrogen to carbon source ratio demonstrated that biological Cr(VI) reduction is associated to the cell multiplication phase; as a result, maximum Cr(VI) removal rates occur when there is no substrate limitation. The biomass can be acclimated to the presence of Cr(VI) and generate new cells that maintain the ability to reduce chromate. Therefore, the activated sludge process could be applied to a continuous Cr(VI) removal process.

  10. Removal of Cr(VI) from aqueous solution by flocculant with the capacity of reduction and chelation

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Gang, E-mail: gangw99@163.com [School of Environmental and Municipal Engineering, Lanzhou Jiaotong University, Lanzhou, Gansu 730070 (China); Chang, Qing; Han, Xiaoting; Zhang, Mingyue [School of Environmental and Municipal Engineering, Lanzhou Jiaotong University, Lanzhou, Gansu 730070 (China)

    2013-03-15

    Highlights: ► We report a novel flocculant with the properties of reduction and chelation for Cr. ► The removal of Cr(VI) by the flocculant depends highly on pH value. ► Some coexisting ions inhibit Cr (VI) removal, but promote total Cr removal. ► Cr and turbidity can be removed simultaneously in the treated wastewater. ► The interaction mechanism is investigated by FTIR and SEM. -- Abstract: A novel agent polyethyleneimine-sodium xanthogenate (PEX) with the multifunction of reduction, chelation, flocculation and precipitation was synthesized by using polyethyleneimine (PEI), carbon disulfide (CS{sub 2}), and sodium hydroxide (NaOH). The effects of different important parameters, such as pH value, initial Cr(VI) concentration, coexisting ions and turbidity etc., on the removal of chromium from aqueous solution by PEX were investigated in flocculation experiments. The experiments results demonstrated that PEX could efficiently remove Cr(VI) and total Cr (Cr(VI) + Cr(III)) in strongly acidic media. It was proved that the presence of coexisting ions (Na{sup +}, Ca{sup 2+}, F{sup −}, Cl{sup −}, and SO{sub 4}{sup 2−}) in the solution had a little influence on the removal of chromium. Furthermore, it was conformed that Cr(VI) ions and turbidity could be simultaneously removed when water samples contained both Cr(VI) ions and turbidity. Finally, the mechanism of interaction between chromium and PEX was further confirmed by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The results reveal that dithiocarboxylic acid groups on PEX macromolecule play a major role in Cr(VI) reduction and Cr(III) chelation, and the flocs formation is attributed to the interparticle bridging mechanism of PEX.

  11. Laser-induced efficient reduction of Cr(VI) catalyzed by ZnO nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Qamar, M. [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Gondal, M.A., E-mail: magondal@kfupm.edu.sa [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Laser Research Group, Physics Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Yamani, Z.H. [Center of Excellence in Nanotechnology, King Fahd University of Petroleum and Minerals, KFUPM Box 741, Dhahran 31261 (Saudi Arabia); Laser Research Group, Physics Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia)

    2011-03-15

    The present study demonstrates the complete removal of Cr(VI) in aqueous suspensions of zinc oxide nanoparticles using a novel laser-induced photocatalytic process without the use of any additive. The study showed that {approx}95% Cr(VI) was removed within short time (60 min) of laser exposure in the presence of ZnO. However, the removal of chromium using conventional setup under identical conditions was found to be negligible. Effect of critical parameters, such as laser energy, catalyst concentration, chromium concentration, and added electron donor and acceptor on the photocatalytic reduction process was also investigated. The data regarding temporal behavior of metal removal was fitted to first-order kinetic and reaction rate was computed.

  12. Chromium isotopic fractionation during Cr(VI) reduction by Bacillus sp. under aerobic conditions.

    Science.gov (United States)

    Xu, Fen; Ma, Teng; Zhou, Lian; Hu, Zhifang; Shi, Liu

    2015-07-01

    This study investigated the fractionation of chromium isotopes during chromium reduction by Bacillus sp. under aerobic condition, variable carbon source (glucose) concentration (0, 0.1, 1, 2.5 and 10mM), and incubation temperatures (4, 15, 25 and 37°C). The results revealed that the δ(53)Cr values in the residual Cr(VI) increased with the degree of Cr reduction, and followed a Rayleigh fractionation model. The addition of glucose only slightly affected cell-specific Cr(VI) reduction rates (cSRR). However, the value of ε (2.00±0.21‰) in the experiments with different concentrations of glucose (0.1, 1, 2.5 and 10mM) was smaller than that from the experiment without glucose (3.74±0.16‰). The results indicated that the cell-specific reduction rate is not the sole control on the degree of isotopic fractionation, and different metabolic pathways would result in differing degrees of Cr isotopic fractionation. The cSRR decreased with decreasing temperature, showing that the values of ε were 7.62±0.36‰, 4.59±0.28‰, 3.09±0.16‰ and 1.99±0.23‰ at temperatures of 4, 15, 25 and 37°C, respectively. It shown that increasing cSRR linked to decreasing fractionations has been associated with increasing temperatures. Overall, our results revealed that temperature is a primary factor affecting Cr isotopic fractionation under microbial actions. Copyright © 2015 Elsevier Ltd. All rights reserved.

  13. Pyrolysis Treatment of Chromite Ore Processing Residue by Biomass: Cellulose Pyrolysis and Cr(VI) Reduction Behavior.

    Science.gov (United States)

    Zhang, Da-Lei; Zhang, Mei-Yi; Zhang, Chu-Hui; Sun, Ying-Jie; Sun, Xiao; Yuan, Xian-Zheng

    2016-03-15

    The pyrolysis treatment with biomass is a promising technology for the remediation of chromite-ore-processing residue (COPR). However, the mechanism of this process is still unclear. In this study, the behavior of pyrolysis reduction of Cr(VI) by cellulose, the main component of biomass, was elucidated. The results showed that the volatile fraction (VF) of cellulose, ie. gas and tar, was responsible for Cr(VI) reduction. All organic compounds, as well as CO and H2 in VF, potentially reduced Cr(VI). X-ray absorption near-edge structure (XANES) spectroscopy and extended X-ray absorption fine-structure (EXAFS) spectroscopy confirmed the reduction of Cr(VI) to Cr(III) and the formation of amorphous Cr2O3. The remnant Cr(VI) content in COPR can be reduced below the detection limit (2 mg/kg) by the reduction of COPR particle and extension of reaction time between VF and COPR. This study provided a deep insight on the co-pyrolysis of cellulose with Cr(VI) in COPR and an ideal approach by which to characterize and optimize the pyrolysis treatment for COPR by other organics.

  14. Influence of operational parameters and kinetics analysis on the photocatalytic reduction of Cr(VI) by immobilized ZnO.

    Science.gov (United States)

    Behnajady, Mohammad A; Mansoriieh, Nafiseh; Modirshahla, Nasser; Shokri, Mohammad

    2012-01-01

    In the present work the performance of immobilized ZnO on a glass plate with the heat attachment method has been described for photoreduction of Cr(VI) to the less harmful Cr(III) at different operational parameters. The photoreduction of Cr(VI) on the surface of the immobilized ZnO catalyst was studied as a function of the pH of solution, initial Cr(VI) concentration and ultraviolet (UV) light intensity. Results indicated that the reduction rate decreases with increasing initial concentration of Cr(VI) and initial pH of solution, whereas it increases with increasing UV light intensity. The photoreduction rate of Cr(VI) on the surface of the immobilized ZnO in the presence of O2 as mobile gas is more than Ar and N2. The reduction process of Cr(VI) by immobilized ZnO also could be done under visible light irradiation. Pseudo first-order kinetics were observed for the photoreduction of Cr(VI) at different operational conditions. With non-linear regression analysis a mathematical kinetics model was developed for the pseudo first-order constant (k(ap)) as a function of operational parameters.

  15. Removal of chromium from Cr(VI) polluted wastewaters by reduction with scrap iron and subsequent precipitation of resulted cations.

    Science.gov (United States)

    Gheju, M; Balcu, I

    2011-11-30

    This work presents investigations on the total removal of chromium from Cr(VI) aqueous solutions by reduction with scrap iron and subsequent precipitation of the resulted cations with NaOH. The process was detrimentally affected by a compactly passivation film occurred at scrap iron surface, mainly composed of Cr(III) and Fe(III). Maximum removal efficiency of the Cr(total) and Fe(total) achieved in the clarifier under circumneutral and alkaline (pH 9.1) conditions was 98.5% and 100%, respectively. The optimum precipitation pH range which resulted from this study is 7.6-8.0. Fe(total) and Cr(total) were almost entirely removed in the clarifier as Fe(III) and Cr(III) species; however, after Cr(VI) breakthrough in column effluent, chromium was partially removed in the clarifier also as Cr(VI), by coprecipitation with cationic species. As long the column effluent was free of Cr(VI), the average Cr(total) removal efficiency of the packed column and clarifier was 10.8% and 78.8%, respectively. Our results clearly indicated that Cr(VI) contaminated wastewater can be successfully treated by combining reduction with scrap iron and chemical precipitation with NaOH. Copyright © 2011 Elsevier B.V. All rights reserved.

  16. Cr (VI electromechimal reduction using RVG 4OOO graphite felt as the electrode

    Directory of Open Access Journals (Sweden)

    E.O. Vilar

    2003-09-01

    Full Text Available Even in at very low concentrations, heavy metals in industrial waste constitute environmental and health risks. The U.S. Department of Health and Human Services has recognized as chromium compounds and defined carcinogens the level acceptable in drinking water as being only 0.05 ppm. The objective of this work was the electrochemical reduction of hexavalent chromium Cr (VI to Cr (III ions in a dilute synthetic solution of K2Cr2O7 and Na2SO4 (0.05N. A plug-flow reactor with an RVG 4000 graphite felt (Le Carbone Lorraine, France electrode was used for this work. Its morphological characteristics such as specific variables surface, porosity, average fibre diameter and permeability were determined. The influencing process selectivity such as initial concentration of Cr (VI, solution pH, current intensity and conversion yield are considered. The fractional conversion achieved in the plug-flow reactor in the present work, was about 90%.

  17. Reduction of Cr(VI) to Cr(III) in Artificially-Contaminated Soil using Chemical Reagents

    Science.gov (United States)

    Kostarelos, Konstantinos; Rao, Ennio; Reale, Daniela

    2010-05-01

    The presence of hexavalent chromium (CrVI) in soil is an environmental concern due to its effect on human health. The concern arises from the leaching and the seepage of Cr(VI) from soil to groundwater. A remediation approach that has been studied in the literature is that of reducing the hexavalent chromium to its trivalent form using a chemical reagent, namely ferrous sulfate heptahydrate (FeSO4.7H20). In this study, we compared performance of ferrous sulfate heptahydrate to sodium thiosulfate (Na2S2O3), a less costly reductant. The means of measuring the performance of the reductants is the US EPA's Toxicity Characteristic Leaching Procedure (TCLP), which states that the total chromium release from the soil must be less than 5 ppm. Because this treatment approach is pH sensitive and thus, susceptible to acid rain effects, it was studied with the intention that it be coupled with a stabilization/fixation approach so as to provide a second level of treatment; i.e., it is not intended to be the stand-alone treatment approach. In this study, the reductants were initially used to treat a contaminated, artificial soil and allowed to cure for varying time periods to determine the minimum curing time. Contaminated artificial soil were then prepared using the same percentage of white sand, kaolinite clay and potassium chromate and varying amount of water as a function of the humidity of the specimens in order to illucidate the effect of moisture on the reductant performance. Finally, the reductant (either ferrous sulfate heptahydrate or sodium thiosulfate) was added in varying doses to determine the best ratio Cr/reagent dose. Chromium release from the soil was evaluated with a modified Toxicity Characteristic Leaching Procedure (TCLP) test after allowing the samples to cure. Results indicated that chromium(VI) released from the specimens was less than 5 ppm for the samples treated with either ferrous sulfate heptahydrate (99.9% of reduction) and sodium thiosulfate (98

  18. Characterizations of nano-TiO{sub 2}/diatomite composites and their photocatalytic reduction of aqueous Cr (VI)

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Qing; Li, Hui; Zheng, Shuilin, E-mail: shuilinzh@sina.com; Sun, Zhiming, E-mail: szmcumtb@hotmail.com

    2014-08-30

    Graphical abstract: Nano-TiO{sub 2}/diatomite (DIA) composites were successfully synthesized by a typical hydrolysis precipitation method. The composites show good photocatalytic activity and stability for aqueous Cr (VI) removal. - Highlights: • TiO{sub 2} nanoparticles/diatomite composite was synthesized and characterized. • The composite exhibited a good photocatalytic performance in Cr (VI) reduction. • The photocatalyst showed good photocatalytic stability. • The composite is a promising material for Cr (VI) photocatalytic reduction. - Abstract: In this paper, the TiO{sub 2} nanoparticles were immobilized on diatomite (DIA) via a typical hydrolysis precipitation process using TiCl{sub 4} as precursor. The as-prepared composites were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). TiO{sub 2} nanoparticles with the average grain size of around 7–14 nm were well deposited on the surface of diatomite. The photocatalytic activity toward the reduction of aqueous Cr (VI) was demonstrated under UV light. The influence of initial pH values, catalyst amount, illumination intensity and initial concentration of Cr (VI) on photocatalytic reduction of Cr (VI) were investigated. Compared with the commercial TiO{sub 2} (P25, Degussa), the TiO{sub 2}/DIA composites had better reactive activity because of their relatively higher adsorption capacity. Furthermore, the prepared photocatalyst exhibited relatively good photocatalytic stability depending on the reusability tests.

  19. Hexagonal 2H-MoSe2 broad spectrum active photocatalyst for Cr(VI) reduction

    OpenAIRE

    Haipeng Chu; Xinjuan Liu; Baibai Liu; Guang Zhu; Wenyan Lei; Huigang Du; Junying Liu; Jianwei Li; Can Li; Changqing Sun

    2016-01-01

    To make full use of the solar energy, exploring broad spectrum active photocatalysts has become one of the core issues for photocatalysis. Here we report a novel hexagonal 2H-MoSe2 photocatalyst with ultraviolet (UV)-visible-near infrared (NIR) light response for the first time. The results indicate that the MoSe2 displays excellent photo-absorption and photocatalytic activity in the reduction of Cr(VI) under UV and visible even NIR light irradiation. MoSe2 synthesized at pH value of 2 achiev...

  20. Cr(VI) reduction and Cr(III) immobilization by resting cells of Pseudomonas aeruginosa CCTCC AB93066: spectroscopic, microscopic, and mass balance analysis.

    Science.gov (United States)

    Kang, Chunxi; Wu, Pingxiao; Li, Liping; Yu, Langfeng; Ruan, Bo; Gong, Beini; Zhu, Nengwu

    2017-02-01

    The aim of this study was to investigate the mechanism of Cr(VI) reduction and Cr(III) immobilization by resting cells of Pseudomonas aeruginosa using batch experiments and analysis techniques. Data showed that resting cells of this strain (3.2 g/L dry weight) reduced 10 mg/L of Cr(VI) by 86% in Tris-HCl buffer solution under optimized conditions of 5 g/L of sodium acetate as an electron donor, pH of 7.0 and temperature of 37 °C within 24 h. Cr(VI) was largely converted to nontoxic Cr(III), and both soluble crude cell-free extracts and membrane-associated fractions were responsible for Cr(VI) reduction. While remnant Cr(VI) existed only in the supernatant, the content of resultant Cr(III) in supernatant, on cell surface and inside cells was 2.62, 1.06, and 5.07 mg/L, respectively, which was an indicative of extracellular and intracellular reduction of chromate. Scanning electron microscopy analysis combined with energy dispersive X-ray spectroscopy revealed the adsorption of chromium on the bacterial surface. Interaction between Cr(III) and cell surface functional groups immobilized Cr(III) as indicated by Fourier transform infrared analyses and X-ray photoelectron spectroscopy. Transmission electron microscopy revealed Cr(III) precipitates in bacterial interior suggesting that Cr(II) could also be intracellularly accumulated. Thus, it can be concluded that interior and exterior surfaces of resting P. aeruginosa cells were sites for reduction and immobilization of Cr(VI) and Cr(III), respectively. This is further insight into the underlying mechanisms of microbial chromate reduction.

  1. Hexagonal 2H-MoSe2 broad spectrum active photocatalyst for Cr(VI) reduction

    Science.gov (United States)

    Chu, Haipeng; Liu, Xinjuan; Liu, Baibai; Zhu, Guang; Lei, Wenyan; Du, Huigang; Liu, Junying; Li, Jianwei; Li, Can; Sun, Changqing

    2016-10-01

    To make full use of the solar energy, exploring broad spectrum active photocatalysts has become one of the core issues for photocatalysis. Here we report a novel hexagonal 2H-MoSe2 photocatalyst with ultraviolet (UV)-visible-near infrared (NIR) light response for the first time. The results indicate that the MoSe2 displays excellent photo-absorption and photocatalytic activity in the reduction of Cr(VI) under UV and visible even NIR light irradiation. MoSe2 synthesized at pH value of 2 achieves the highest Cr(VI) reduction rates of 99%, 91% and 100% under UV, visible and NIR light irradiation, respectively, which should be attributed to its comparatively higher light absorption, efficient charge separation and transfer as well as relatively large number of surface active sites. The excellent broad spectrum active photocatalytic activity makes the MoSe2 to be a promising photocatalyst for the effective utilization of solar energy.

  2. Palladium nanoparticles as catalysts for reduction of Cr(VI) and Suzuki coupling reaction

    Science.gov (United States)

    Zhang, Lilan; Guo, Yali; Iqbal, Anam; Li, Bo; Deng, Min; Gong, Deyan; Liu, Weisheng; Qin, Wenwu

    2017-04-01

    Herein, six kinds of PdNPs (including icosahedron, sphere, spindle, cube, rod, and wire) were synthesized via simple methods. The catalytic activities were investigated by the reduction reaction of Cr(VI) and Suzuki coupling reaction. Chemically synthesized morphologies of the six catalysis were characterized by transmission electron microscopy, field emission scanning electron microscopy, and X-ray diffraction, etc. Pd icosahedron shows a better catalytic property than other PdNPs with a rate constants 0.42 min-1 for the reduction of Cr(VI). Moreover, the electrocatalyst shows that Pd icosahedron possesses a bigger surface area of 8.56 m2/g than other nanoparticles, which is attributed to the better catalyst. The Pd icosahedron possesses a better catalytic property, attributing to the abundant exposed {111} facets with high activity on Pd icosahedron. The catalytic activities are closely related to the surface area with the following order: icosahedrons ≥ sphere > rod > spindle > cube > wire. The Pd icosahedron catalyst represents a strong activity for Suzuki coupling reaction as well, outweighting is 80%. The results reveal that Pd icosahedron acts as an efficient catalyst compared to other PdNPs (wire, rod, sphere, spindle, and cube).

  3. Palladium nanoparticles as catalysts for reduction of Cr(VI) and Suzuki coupling reaction

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Lilan; Guo, Yali; Iqbal, Anam; Li, Bo; Deng, Min; Gong, Deyan; Liu, Weisheng; Qin, Wenwu, E-mail: qinww@lzu.edu.cn [Lanzhou University, Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province and State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering (China)

    2017-04-15

    Herein, six kinds of PdNPs (including icosahedron, sphere, spindle, cube, rod, and wire) were synthesized via simple methods. The catalytic activities were investigated by the reduction reaction of Cr(VI) and Suzuki coupling reaction. Chemically synthesized morphologies of the six catalysis were characterized by transmission electron microscopy, field emission scanning electron microscopy, and X-ray diffraction, etc. Pd icosahedron shows a better catalytic property than other PdNPs with a rate constants 0.42 min{sup −1} for the reduction of Cr(VI). Moreover, the electrocatalyst shows that Pd icosahedron possesses a bigger surface area of 8.56 m{sup 2}/g than other nanoparticles, which is attributed to the better catalyst. The Pd icosahedron possesses a better catalytic property, attributing to the abundant exposed {111} facets with high activity on Pd icosahedron. The catalytic activities are closely related to the surface area with the following order: icosahedrons ≥ sphere > rod > spindle > cube > wire. The Pd icosahedron catalyst represents a strong activity for Suzuki coupling reaction as well, outweighting is 80%. The results reveal that Pd icosahedron acts as an efficient catalyst compared to other PdNPs (wire, rod, sphere, spindle, and cube).

  4. Single-cell imaging and spectroscopic analyses of Cr(VI) reduction on the surface of bacterial cells.

    Science.gov (United States)

    Wang, Yuanmin; Sevinc, Papatya C; Belchik, Sara M; Fredrickson, Jim; Shi, Liang; Lu, H Peter

    2013-01-22

    We investigate the single-cell reduction of toxic Cr(VI) by the dissimilatory metal-reducing bacterium Shewanella oneidensis MR-1 (MR-1), an important bioremediation process, using Raman spectroscopy and scanning electron microscopy (SEM) combined with energy-dispersive X-ray spectroscopy (EDX). Our experiments indicate that the toxic, highly soluble Cr(VI) can be efficiently reduced to less toxic, nonsoluble Cr(2)O(3) nanoparticles by MR-1. Cr(2)O(3) is observed to emerge as nanoparticles adsorbed on the cell surface and its chemical nature is identified by EDX imaging and Raman spectroscopy. Co-localization of Cr(2)O(3) and cytochromes by EDX imaging and Raman spectroscopy suggests a terminal reductase role for MR-1 surface-exposed cytochromes MtrC and OmcA. Our experiments revealed that the cooperation of surface proteins OmcA and MtrC makes the reduction reaction most efficient, and the sequence of the reducing reactivity of MR-1 is wild type > single mutant ΔmtrC or mutant ΔomcA > double mutant (ΔomcA-ΔmtrC). Moreover, our results also suggest that direct microbial Cr(VI) reduction and Fe(II) (hematite)-mediated Cr(VI) reduction mechanisms may coexist in the reduction processes.

  5. Assessing the Cr(VI) reduction efficiency of a permeable reactive barrier using Cr isotope measurements and 2D reactive transport modeling.

    Science.gov (United States)

    Wanner, Christoph; Zink, Sonja; Eggenberger, Urs; Mäder, Urs

    2012-04-01

    In Thun, Switzerland, a permeable reactive barrier (PRB) for Cr(VI) reduction by gray cast iron was installed in May 2008. The PRB is composed of a double array of vertical piles containing iron shavings and gravel. The aquifer in Thun is almost saturated with dissolved oxygen and the groundwater flow velocities are ca. 10-15m/day. Two years after PRB installation Cr(VI) concentrations still permanently exceed the Swiss threshold value for contaminated sites downstream of the barrier at selected localities. Groundwater δ(53/52)Cr(SRM979) measurements were used to track Cr(VI) reduction induced by the PRB. δ(53/52)Cr(SRM979) values of two samples downstream of the PRB showed a clear fractionation towards more positive values compared to four samples from the hotspot, which is clear evidence of Cr(VI) reduction induced by the PRB. Another downstream sample did not show a shift to more positive δ(53/52)Cr(SRM979) values. Because this latter location correlates with the highest downstream Cr(VI) concentration it is proposed that a part of the Cr(VI) plume is bypassing the barrier. Using a Rayleigh fractionation model a minimum present-day overall Cr(VI) reduction efficiency of ca. 15% was estimated. A series of 2D model simulations, including the fractionation of Cr isotopes, confirm that only a PRB bypass of parts of the Cr(VI) plume can lead to the observed values. Additionally, the simulations revealed that the proposed bypass occurs due to an insufficient permeability of the individual PRB piles. It is concluded that with this type of PRB a complete and long-lasting Cr(VI) reduction is extremely difficult to achieve for Cr(VI) contaminations located in nearly oxygen and calcium carbonate saturated aquifer in a regime of high groundwater velocities. Additional remediation action would limit the environmental impact and allow to reach target concentrations. Copyright © 2012 Elsevier B.V. All rights reserved.

  6. Photocatalytic Reduction of Aqueous Cr(VI with CdS under Visible Light Irradiation: Effect of Particle Size

    Directory of Open Access Journals (Sweden)

    A. B. Makama

    2017-04-01

    Full Text Available Stringent environmental standards have made the removal of Cr(VI from water an important problem for environmental scientist and engineering. Heterogeneous photocatalysis using suspended photocatalyst is an interesting technique to consider for this application. In this work, the influence of particle size of suspended CdS on the photocatalytic reduction of aqueous Cr(VI ion was investigated. The efficiency of Cr(VI reduction was monitored through UV-visible analysis. The experimental results showed that the nanoparticle size has a dramatic effect on the adsorption and reduction of Cr(VI. As surface area increased from 44.2±0.6 to 98.7±0.5 m2/g due to particle size reduction, the rate of Cr(VI reduction nearly doubled in the first 20 min of visible light irradiation. The results evidenced the inverse relationship between the apparent reduction rate constant and the CdS particle size. Conversely, the half-life (t1/2 period of the photocatalytic reduction has a direct relationship with CdS particle sizes. Copyright © 2017 BCREC GROUP. All rights reserved Received: 14th July 2016; Revised: 11st October 2016; Accepted: 18th October 2016 How to Cite: Makama, A.B., Salmiaton, A., Saion, E.B., Choong, T.S.Y., Abdullah, N. (2017. Photocatalytic Reduction of Aqueous Cr(VI with CdS under Visible Light Irradiation: Effect of Particle Size. Bulletin of Chemical Reaction Engineering & Catalysis, 12(1: 62-70 (doi:10.9767/bcrec.12.1.593.62-70 Permalink/DOI: http://dx.doi.org/10.9767/bcrec.12.1.593.62-70

  7. Selective Reduction of Cr(VI in Chromium, Copper and Arsenic (CCA Mixed Waste Streams Using UV/TiO2 Photocatalysis

    Directory of Open Access Journals (Sweden)

    Shan Zheng

    2015-02-01

    Full Text Available The highly toxic Cr(VI is a critical component in the Chromated Copper Arsenate (CCA formulations extensively employed as wood preservatives. Remediation of CCA mixed waste and discarded treated wood products is a significant challenge. We demonstrate that UV/TiO2 photocatalysis effectively reduces Cr(VI to less toxic Cr(III in the presence of arsenate, As(V, and copper, Cu(II. The rapid conversion of Cr(VI to Cr(III during UV/TiO2 photocatalysis occurs over a range of concentrations, solution pH and at different Cr:As:Cu ratios. The reduction follows pseudo-first order kinetics and increases with decreasing solution pH. Saturation of the reaction solution with argon during UV/TiO2 photocatalysis had no significant effect on the Cr(VI reduction demonstrating the reduction of Cr(VI is independent of dissolved oxygen. Reduction of Cu(II and As(V does not occur under the photocatalytic conditions employed herein and the presence of these two in the tertiary mixtures had a minimal effect on Cr(VI reduction. The Cr(VI reduction was however, significantly enhanced by the addition of formic acid, which can act as a hole scavenger and enhance the reduction processes initiated by the conduction band electron. Our results demonstrate UV/TiO2 photocatalysis effectively reduces Cr(VI in mixed waste streams under a variety of conditions.

  8. Selective reduction of Cr(VI) in chromium, copper and arsenic (CCA) mixed waste streams using UV/TiO2 photocatalysis.

    Science.gov (United States)

    Zheng, Shan; Jiang, Wenjun; Rashid, Mamun; Cai, Yong; Dionysiou, Dionysios D; O'Shea, Kevin E

    2015-02-03

    The highly toxic Cr(VI) is a critical component in the Chromated Copper Arsenate (CCA) formulations extensively employed as wood preservatives. Remediation of CCA mixed waste and discarded treated wood products is a significant challenge. We demonstrate that UV/TiO2 photocatalysis effectively reduces Cr(VI) to less toxic Cr(III) in the presence of arsenate, As(V), and copper, Cu(II). The rapid conversion of Cr(VI) to Cr(III) during UV/TiO2 photocatalysis occurs over a range of concentrations, solution pH and at different Cr:As:Cu ratios. The reduction follows pseudo-first order kinetics and increases with decreasing solution pH. Saturation of the reaction solution with argon during UV/TiO2 photocatalysis had no significant effect on the Cr(VI) reduction demonstrating the reduction of Cr(VI) is independent of dissolved oxygen. Reduction of Cu(II) and As(V) does not occur under the photocatalytic conditions employed herein and the presence of these two in the tertiary mixtures had a minimal effect on Cr(VI) reduction. The Cr(VI) reduction was however, significantly enhanced by the addition of formic acid, which can act as a hole scavenger and enhance the reduction processes initiated by the conduction band electron. Our results demonstrate UV/TiO2 photocatalysis effectively reduces Cr(VI) in mixed waste streams under a variety of conditions.

  9. Enhanced Cr(VI) reduction and As(III) oxidation in ice phase: Important role of dissolved organic matter from biochar

    Energy Technology Data Exchange (ETDEWEB)

    Dong, Xiaoling [Department of Soil and Water Science, University of Florida, Gainesville, FL 32611 (United States); Ma, Lena Q., E-mail: lqma@ufl.edu [State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Jiangsu 210046 (China); Department of Soil and Water Science, University of Florida, Gainesville, FL 32611 (United States); Gress, Julia; Harris, Willie [Department of Soil and Water Science, University of Florida, Gainesville, FL 32611 (United States); Li, Yuncong [Soil and Water Science Department, Tropical Research and Education Center, University of Florida, Homestead, FL 33031-3314 (United States)

    2014-02-01

    Graphical abstract: - Highlights: • Biochar-derived dissolved organic matter (DOM) effectively reduced Cr(VI) and oxidized As(III). • Cr(VI) and As(III) could serve as a redox couple. • Cr(VI) and As(III) redox conversion was more effective in the ice phase than aqueous phase. • FTIR and ESR showed that biochar DOM served as both electron donor and acceptor. - Abstract: This study evaluated the impact of DOM from two biochars (sugar beet tailing and Brazilian pepper) on Cr(VI) reduction and As(III) oxidation in both ice and aqueous phases with a soil DOM as control. Increasing DOM concentration from 3 to 300 mg C L{sup −1} enhanced Cr(VI) reduction from 20% to 100% and As(III) oxidation from 6.2% to 25%; however, Cr(VI) reduction decreased from 80–86% to negligible while As(III) oxidation increased from negligible to 18–19% with increasing pH from 2 to 10. Electron spin resonance study suggested semiquinone radicals in DOM were involved in As(III) oxidation while Fourier transform infrared analysis suggested that carboxylic groups in DOM participated in both Cr(VI) reduction and As(III) oxidation. During Cr(VI) reduction, part of DOM (∼10%) was oxidized to CO{sub 2}. The enhanced conversion of Cr(VI) and As(III) in the ice phase was due to the freeze concentration effect with elevated concentrations of electron donors and electron acceptors in the grain boundary. Though DOM enhanced both Cr(VI) reduction and As(III)oxidation, Cr(VI) reduction coupled with As(III) oxidation occurred in absence of DOM. The role of DOM, Cr(VI) and/or As(III) in Cr and As transformation may provide new insights into their speciation and toxicity in cold regions.

  10. Permeable Reactive Biobarriers for In Situ Cr(VI) Reduction: Bench Scale Tests Using Cellulomonas sp. Strain ES6

    Energy Technology Data Exchange (ETDEWEB)

    Sridhar Viamajala; Brent M. Peyton; Robin Gerlach; Vaideeswaran; William A. Apel; James N. Petersen

    2008-12-01

    Chromate (Cr(VI)) reduction studies were performed in bench scale flow columns using the fermentative subsurface isolate Cellulomonas sp. strain ES6. In these tests, columns packed with either quartz sand or hydrous ferric oxide (HFO)-coated quartz sand, were inoculated with strain ES6 and fed nutrients to stimulate growth before nutrient-free Cr(VI) solutions were injected. Results show that in columns containing quartz sand, a continuous inflow of 2 mg/L Cr(VI) was reduced to below detection limits in the effluent for durations of up to 5.7 residence times after nutrient injection was discontinued proving the ability of strain ES6 to reduce chromate in the absence of an external electron donor. In the HFO-containing columns, Cr(VI) reduction was significantly prolonged and effluent Cr(VI) concentrations remained below detectable levels for periods of up to 66 residence times after nutrient injection was discontinued. Fe was detected in the effluent of the HFO-containing columns throughout the period of Cr(VI) removal indicating that the insoluble Fe(III) bearing solids were being continuously reduced to form soluble Fe(II) resulting in prolonged abiotic Cr(VI) reduction. Thus, growth of Cellulomonas within the soil columns resulted in formation of permeable reactive barriers that could reduce Cr(VI) and Fe(III) for extended periods even in the absence of external electron donors. Other bioremediation systems employing Fe(II)-mediated reactions require a continuous presence of external nutrients to regenerate Fe(II). After depletion of nutrients, contaminant removal within these systems occurs by reaction with surface-associated Fe(II) that can rapidly become inaccessible due to formation of crystalline Fe-minerals or other precipitates. The ability of fermentative organisms like Cellulomonas to reduce metals without continuous nutrient supply in the subsurface offers a viable and economical alternative technology for in situ remediation of Cr(VI

  11. Permeable reactive biobarriers for in situ Cr(VI) reduction: bench scale tests using Cellulomonas sp. strain ES6.

    Science.gov (United States)

    Viamajala, Sridhar; Peyton, Brent M; Gerlach, Robin; Sivaswamy, Vaideeswaran; Apel, William A; Petersen, James N

    2008-12-15

    Chromate (Cr(VI)) reduction studies were performed in bench scale flow columns using the fermentative subsurface isolate Cellulomonas sp. strain ES6. In these tests, columns packed with either quartz sand or hydrous ferric oxide (HFO)-coated quartz sand, were inoculated with strain ES6 and fed nutrients to stimulate growth before nutrient-free Cr(VI) solutions were injected. Results show that in columns containing quartz sand, a continuous inflow of 2 mg/L Cr(VI) was reduced to below detection limits in the effluent for durations of up to 5.7 residence times after nutrient injection was discontinued proving the ability of strain ES6 to reduce chromate in the absence of an external electron donor. In the HFO-containing columns, Cr(VI) reduction was significantly prolonged and effluent Cr(VI) concentrations remained below detectable levels for periods of up to 66 residence times after nutrient injection was discontinued. Fe was detected in the effluent of the HFO-containing columns throughout the period of Cr(VI) removal indicating that the insoluble Fe(III) bearing solids were being continuously reduced to form soluble Fe(II) resulting in prolonged abiotic Cr(VI) reduction. Thus, growth of Cellulomonas within the soil columns resulted in formation of permeable reactive barriers that could reduce Cr(VI) and Fe(III) for extended periods even in the absence of external electron donors. Other bioremediation systems employing Fe(II)-mediated reactions require a continuous presence of external nutrients to regenerate Fe(II). After depletion of nutrients, contaminant removal within these systems occurs by reaction with surface-associated Fe(II) that can rapidly become inaccessible due to formation of crystalline Fe-minerals or other precipitates. The ability of fermentative organisms like Cellulomonas to reduce metals without continuous nutrient supply in the subsurface offers a viable and economical alternative technology for in situ remediation of Cr(VI

  12. Accumulation of amorphous Cr(III)-Te(IV) nanoparticles on the surface of Shewanella oneidensis MR-1 through reduction of Cr(VI).

    Science.gov (United States)

    Kim, Dong-Hun; Park, Sunhwa; Kim, Min-Gyu; Hur, Hor-Gil

    2014-12-16

    Industrial effluents constitute a major source of metal pollution of aquatic bodies. Moreover, due to their environmental persistence, toxic metal pollution is of special concern. Microbial reduction is considered a promising strategy for toxic metal removal among the several methods available for metal remediation. Here, we describe the coremediation of toxic Cr(VI) and Te(IV) by the dissimilatory metal reducing bacterium-Shewanella oneidensis MR-1. In the presence of both Cr(VI) and Te(IV), S. oneidensis MR-1 reduced Cr(VI) to the less toxic Cr(III) form, but not Te(IV) to Te(0). The reduced Cr(III) ions complexed rapidly with Te(IV) ions and were precipitated from the cell cultures. Electron microscopic analyses revealed that the Cr-Te complexed nanoparticles localized on the bacterial outer membranes. K-edge X-ray absorption spectrometric analyses demonstrated that Cr(III) produced by S. oneidensis MR-1 was rapidly complexed with Te(IV) ions, followed by formation of amorphous Cr(III)-Te(IV) nanoparticles on the cell surface. Our results could be applied for the simultaneous sequestration and detoxification of both Cr(VI) and Te(IV) as well as for the preparation of nanomaterials through environmental friendly processes.

  13. Removal of Cr(VI) ions by sewage sludge compost biomass from aqueous solutions: Reduction to Cr(III) and biosorption

    Science.gov (United States)

    Chen, Huixia; Dou, Junfeng; Xu, Hongbin

    2017-12-01

    Sewage sludge compost biomass was used as a novel biosorbent to remove hexavalent chromium from water. Surface area analysis, scanning electron microscopy, fourier-transform infrared spectroscopy, energy-dispersive X-ray spectroscopy, and point zero charge was applied to study the microstructure, compositions and chemical bonding states of the biomass adsorbent. Effects of contact time, biomass dosage, agitation speed, pH, the initial concentration of Cr(VI) and Cr(Ⅲ) on its adsorption removal were also performed in the batch experiments. A model describing adsorption, desorption and reduction phenomena during the sorption process has been referenced to model Cr(VI) sorption onto sewage sludge compost biomass. The result of characterization test shows that adsorption of Cr(VI) onto sewage sludge compost biomass followed by the partial reduction to Cr(Ⅲ) by biomass groups such as hydroxyl, carboxyl, and amino groups. The absorption kinetics model in the description of adsorption-coupled reduction of Cr(VI) fits successfully the kinetic data obtained at different temperatures and describes the kinetics profile of total, hexavalent and trivalent chromium. The study shows that sewage sludge compost biomass could be used as a potential biosorbent for removal of hexavalent chromium from wastewaters.

  14. Environmental remediation of Cr(VI) solutions by photocatalytic reduction using Ag–Er(OH){sub 3} nanocomposite

    Energy Technology Data Exchange (ETDEWEB)

    Malkhasian, Aramice Y.S., E-mail: amalkhasian10@gmail.com [Chemistry Department, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia); Mohamed, Reda M. [Chemistry Department, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia); Advanced Materials Department, Central Metallurgical R& D Institute, CMRDI, P.O. Box 87 Helwan, Cairo (Egypt); Center of Excellence in Environmental Studies, King Abdulaziz University, P.O. Box 80216, Jeddah 21589 (Saudi Arabia)

    2015-05-25

    Highlights: • Ag/Er(OH){sub 3} nanoparticles were used for photocatalytic reduction of Cr(VI). • Photocatalytic reduction of Cr(VI) was dependent on wt% of Ag. • Catalyst re-use revealed the present photocatalyst remain effective and active after five cycles. - Abstract: A hydrothermal method was use to prepare Er(OH){sub 3} nanoparticles, and a photoassisted deposition method was used to deposit silver onto the surface of those nanoparticles. Er(OH){sub 3} and Ag/Er(OH){sub 3} nanocomposites were characterized by BET, XRD, XPS, PL, UV–Vis and TEM measurements. The photocatalytic performance of the nanoparticles with respect to the photocatalytic reduction of chromium(VI) under UV light irradiation was determined. The results reveal that the silver particles were well dispersed onto the surface of the Er(OH){sub 3} nanoparticles. Additionally, the surface area of the Ag/Er(OH){sub 3} nanocomposites was observed to be smaller than that of the Er(OH){sub 3} nanoparticles due to the blocking of some pores of the Er(OH){sub 3} nanoparticles by the deposition of silver particles. The Ag/Er(OH){sub 3} nanocomposites (0.15 wt%) exhibit the lowest band gap and highest photocatalytic activity for the reduction of Cr(VI). The photocatalytic performance of the 0.15 wt% Ag/Er(OH){sub 3} nanocomposites was stable after the reuse of the nanoparticles for the reduction of Cr(VI) after five uses.

  15. Catalytic role of Cu(II) in the reduction of Cr(VI) by citric acid under an irradiation of simulated solar light.

    Science.gov (United States)

    Li, Ying; Chen, Cheng; Zhang, Jing; Lan, Yeqing

    2015-05-01

    The catalytic role of Cu(II) in the reduction of Cr(VI) by citric acid with simulated solar light was investigated. The results demonstrated that Cu(II) could significantly accelerate Cr(VI) reduction and the reaction obeyed to pseudo zero-order kinetics with respect to Cr(VI). The removal of Cr(VI) was related to the initial concentrations of Cu(II), citric acid, and the types of organic acids. The optimal removal of Cr(VI) was achieved at pH 4, and the rates of Cu(II) photocatalytic reduction of Cr(VI) by organic acids were in the order: tartaric acid (two α-OH groups, two -COOH groups)>citric acid (one α-OH group, three -COOH groups)>malic acid (one α-OH group, two -COOH groups)>lactic acid (one α-OH group, one -COOH group)≫succinic acid (two -COOH groups), suggesting that the number of α-OH was the key factor for the reaction, followed by the number of -COOH. The formation of Cu(II)-citric acid complex could generate Cu(I) and radicals through a pathway of metal-ligand-electron transfer, promoting the reduction of Cr(VI). This study is helpful to fully understanding the conversion of Cr(VI) in the existence of both organic acids and Cu(II) with solar light in aquatic environments. Copyright © 2015 Elsevier Ltd. All rights reserved.

  16. Scaling Effects of Cr(VI) Reduction Kinetics. The Role of Geochemical Heterogeneity

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Li [Pennsylvania State Univ., State College, PA (United States); Li, Li [Pennsylvania State Univ., State College, PA (United States)

    2015-10-22

    The natural subsurface is highly heterogeneous with minerals distributed in different spatial patterns. Fundamental understanding of how mineral spatial distribution patterns regulate sorption process is important for predicting the transport and fate of chemicals. Existing studies about the sorption was carried out in well-mixed batch reactors or uniformly packed columns, with few data available on the effects of spatial heterogeneities. As a result, there is a lack of data and understanding on how spatial heterogeneities control sorption processes. In this project, we aim to understand and develop modeling capabilities to predict the sorption of Cr(VI), an omnipresent contaminant in natural systems due to its natural occurrence and industrial utilization. We systematically examine the role of spatial patterns of illite, a common clay, in determining the extent of transport limitation and scaling effects associated with Cr(VI) sorption capacity and kinetics using column experiments and reactive transport modeling. Our results showed that the sorbed mass and rates can differ by an order of magnitude due to of the illite spatial heterogeneities and transport limitation. With constraints from data, we also developed the capabilities of modeling Cr(VI) in heterogeneous media. The developed model is then utilized to understand the general principles that govern the relationship between sorption and connectivity, a key measure of the spatial pattern characteristics. This correlation can be used to estimate Cr(VI) sorption characteristics in heterogeneous porous media. Insights gained here bridge gaps between laboratory and field application in hydrogeology and geochemical field, and advance predictive understanding of reactive transport processes in the natural heterogeneous subsurface. We believe that these findings will be of interest to a large number of environmental geochemists and engineers, hydrogeologists, and those interested in contaminant fate and transport

  17. Experimental and mathematical modeling studies on Cr(VI) reduction by CRB, SRB and IRB, individually and in combination.

    Science.gov (United States)

    Somasundaram, V; Philip, Ligy; Bhallamudi, S Murty

    2009-12-30

    Cr(VI) reduction studies were carried out with chromium reducing bacteria (CRB), sulphate reducing bacteria (SRB) and iron reducing bacteria (IRB), individually and in combination. Biokinetic parameters such as maximum specific growth rate (micro(max)), half saturation constant (K(s)), yield coefficient (Y(T)) and inhibition coefficient (K(i)) for individual cultures were evaluated. A mathematical model was proposed for simulating the chromium reduction, COD utilization and biomass growth, by individual cultures as well as by a combination of two or three different cultures, for different initial Cr(VI), SO(4)(2-) and Fe(III) concentrations. The biokinetic parameters evaluated from one set of experiments for individual cultures were utilized in all the validation studies. The performance of the mathematical model in terms of the dimensionless modified coefficient of efficiency (E) indicated that the proposed model simulates the system behavior very well.

  18. Impregnation synthesis of TiO{sub 2}/hydroniumjarosite composite with enhanced property in photocatalytic reduction of Cr(VI)

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Junjun [Department of Environmental Engineering, College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095 (China); Xu, Zhihui, E-mail: xuzhihui@njau.edu.cn [Department of Chemistry, College of Science, Nanjing Agricultural University, Nanjing 210095 (China); Zhang, Ming [Department of Environmental Engineering, College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095 (China); Xu, Jiangyan [Department of Chemistry, College of Science, Nanjing Agricultural University, Nanjing 210095 (China); Fang, Di, E-mail: Di.Fang@njau.edu.cn [Department of Environmental Engineering, College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095 (China); Ran, Wei [Department of Environmental Engineering, College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095 (China)

    2015-02-15

    In this paper, a series of novel TiO{sub 2}/hydroniumjarosite composite photocatalysts were synthesized by deposition–precipitation method. XRD, UV–vis DRS, TEM, BET, PL spectra and EIS were used to characterize the composite photocatalysts. The photocatalytic performance of the composite catalysts were examined on the Cr(VI) reduction under ultraviolet irradiation in aqueous suspension. The results show that TiO{sub 2}/hydroniumjarosite composites exhibit enhanced photocatalytic activity with a maximum reduction rate of 98.0%, while the Cr(VI) reduction efficiency is only 36.0% over P25 under the same conditions. The increased light absorption intensity and the decreased electron–hole pair recombination rate in TiO{sub 2} with the introduction of hydroniumjarosite are responsible for better catalytic property of TiO{sub 2}/hydroniumjarosite catalysts. It would be of great promise for the industrial application of this catalyst with high potocatalytic performance to reduce Cr(VI) for wastewater treatment. - Highlights: • TiO{sub 2}/hydroniumjarosite with different TiO{sub 2} content was prepared using deposition–precipitation method. • The sample prepared with the TiO{sub 2}/Fe{sup 3+} mole ratio of 75:25 exhibited the highest catalytic efficiency. • The enhanced catalytic activity can be attributed to the formation of TiO{sub 2}/hydroniumjarosite heterostructure.

  19. Hierarchical layered Ni(3)S(2)-graphene hybrid composites for efficient photocatalytic reduction of Cr(VI).

    Science.gov (United States)

    Hu, Pinpin; Liu, Xinjuan; Liu, Baibai; Li, Lei; Qin, Wei; Yu, Huangze; Zhong, Sisi; Li, Yan; Ren, Zhenxing; Wang, Mengliang

    2017-06-15

    Exploring visible light responsive media remains a challenge for solar energy photocatalysis applications. We report the Ni3S2-reduced graphene oxide (NG) hybrid composites with sheet-on-sheet structures synthesized by a facile microwave-assisted method. Their morphology, structure and photocatalytic activity in the reduction of Cr(VI) were characterized by scanning electron microscopy, X-ray diffraction, UV-Vis absorption spectroscopy, and electrochemical impedance spectra, respectively. The results show that NG hybrid composites show excellent visible light photocatalytic activity in the reduction of Cr(VI) compared to pure Ni3S2. The Cr(VI) reduction rate of higher than 90% has been achieved with 1wt.% reduced graphene oxide under visible light irradiation at 180min. Improvement is attributed to its efficient charge separation and more active sites due to the integrative effect and good interfacial contact between Ni3S2 and reduced graphene oxide. Copyright © 2017 Elsevier Inc. All rights reserved.

  20. Selective reduction of Cr(VI) in chromium, copper and arsenic (CCA) mixed waste streams using UV/TiO2 photocatalysis

    National Research Council Canada - National Science Library

    Zheng, Shan; Jiang, Wenjun; Rashid, Mamun; Cai, Yong; Dionysiou, Dionysios D; O'Shea, Kevin E

    2015-01-01

    .... The reduction follows pseudo-first order kinetics and increases with decreasing solution pH. Saturation of the reaction solution with argon during UV/TiO2 photocatalysis had no significant effect on the Cr(VI...

  1. Impact of Fe(III) as an effective electron-shuttle mediator for enhanced Cr(VI) reduction in microbial fuel cells: Reduction of diffusional resistances and cathode overpotentials

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Qiang [Key Laboratory of Industrial Ecology and Environmental Engineering, Ministry of Education (MOE), School of Environmental Science and Technology, Dalian University of Technology, Dalian 116024 (China); Huang, Liping, E-mail: lipinghuang@dlut.edu.cn [Key Laboratory of Industrial Ecology and Environmental Engineering, Ministry of Education (MOE), School of Environmental Science and Technology, Dalian University of Technology, Dalian 116024 (China); Pan, Yuzhen [College of Chemistry, Dalian University of Technology, Dalian 116024 (China); Quan, Xie [Key Laboratory of Industrial Ecology and Environmental Engineering, Ministry of Education (MOE), School of Environmental Science and Technology, Dalian University of Technology, Dalian 116024 (China); Li Puma, Gianluca, E-mail: g.lipuma@lboro.ac.uk [Environmental Nanocatalysis & Photoreaction Engineering, Department of Chemical Engineering, Loughborough University, Loughborough LE11 3TU (United Kingdom)

    2017-01-05

    Highlights: • Fe(III) shuttles electrons for enhanced reduction of Cr(VI) in MFCs. • The coulombic efficiency increases by 1.6 fold in the presence of Fe(III). • The reduction of Cr(VI) occurs via an indirect Fe(III) mediation mechanism. • Fe(III) decreases the diffusional resistances and the cathode overpotentials. - Abstract: The role of Fe(III) was investigated as an electron-shuttle mediator to enhance the reduction rate of the toxic heavy metal hexavalent chromium (Cr(VI)) in wastewaters, using microbial fuel cells (MFCs). The direct reduction of chromate (CrO{sub 4}{sup −}) and dichromate (Cr{sub 2}O{sub 7}{sup 2−}) anions in MFCs was hampered by the electrical repulsion between the negatively charged cathode and Cr(VI) functional groups. In contrast, in the presence of Fe(III), the conversion of Cr(VI) and the cathodic coulombic efficiency in the MFCs were 65.6% and 81.7%, respectively, 1.6 times and 1.4 folds as those recorded in the absence of Fe(III). Multiple analytical approaches, including linear sweep voltammetry, Tafel plot, cyclic voltammetry, electrochemical impedance spectroscopy and kinetic calculations demonstrated that the complete reduction of Cr(VI) occurred through an indirect mechanism mediated by Fe(III). The direct reduction of Cr(VI) with cathode electrons in the presence of Fe(III) was insignificant. Fe(III) played a critical role in decreasing both the diffusional resistance of Cr(VI) species and the overpotential for Cr(VI) reduction. This study demonstrated that the reduction of Cr(VI) in MFCs was effective in the presence of Fe(III), providing an alternative and environmentally benign approach for efficient remediation of Cr(VI) contaminated sites with simultaneous production of renewable energy.

  2. Visible-light-induced photocatalytic reduction of Cr(VI) with coupled Bi2O3/TiO2 photocatalyst and the synergistic bisphenol A oxidation.

    Science.gov (United States)

    Yang, Juan; Dai, Jun; Li, Jiantong

    2013-04-01

    Coupled Bi2O3/TiO2 photocatalysts were fabricated by sol-gel and hydrothermal methods and characterized using various spectroscopy techniques. Photocatalytic reduction of Cr(VI) in aqueous solution, together with the synergistic effect of photodegradation of bisphenol A (BPA), was investigated using these coupled Bi2O3/TiO2 under visible-light irradiation. Coupling of Bi2O3 inhibited the phase transformation from anatase to rutile and extended absorption region to visible light. Bi ions did not enter TiO2 lattice and were more likely to bond with oxygen atoms to form Bi2O3 on the surface of TiO2. Photovoltage signals in visible range revealed the effective interfacial charge transfer between Bi2O3 and TiO2. Two percent Bi2O3/TiO2 exhibited the highest photocatalytic activity of visible-light-induced reduction of Cr(VI). The addition of BPA effectively increased the photocatalytic reduction of Cr(VI). Simultaneously, the presence of Cr(VI) promoted the degradation of BPA, which was demonstrated by the investigation of TOC removal yield and generated intermediates. A possible mechanism of photocatalytic reduction of Cr(VI) and degradation of BPA in Bi2O3/TiO2 system was proposed. The synergistic effect, observed between reduction of Cr(VI) and degradation of BPA, provides beneficial method for environmental remediation and purification of the complex wastewater.

  3. Controlled reduction of red mud waste to produce active systems for environmental applications: heterogeneous Fenton reaction and reduction of Cr(VI).

    Science.gov (United States)

    Costa, Regina C C; Moura, Flávia C C; Oliveira, Patrícia E F; Magalhães, Fabiano; Ardisson, José D; Lago, Rochel M

    2010-02-01

    In this work, controlled reduction of red mud with H(2) was used to produce active systems for two different environmental applications, i.e. the heterogeneous Fenton reaction and the reduction of Cr(VI). Mössbauer, powder X-ray diffraction, thermal analyses and scanning electron microscopy analyses showed that at different temperatures, i.e. 300, 400, 500 and 600 degrees C, H(2) reduces red mud to different phases, mainly Fe(3)O(4), Fe(0)/Fe(3)O(4) and Fe(0). These Fe phases are dispersed on Al, Si and Ti oxides present in the red mud and show high reactivity towards two environmental applications, i.e. the heterogeneous Fenton reaction and the reduction of Cr(VI). Reduction with H(2) at 400 degrees C showed the best results for the oxidation of the model dye methylene blue with H(2)O(2) at neutral pH due to the presence of the composite Fe(0)/Fe(3)O(4). The reduced red mud at 500-600 degrees C produced Fe(0) highly active for the reduction of Cr(VI) in aqueous medium. Another feature of these red mud based system is that after deactivation due to extensive use they can be completely regenerated by simple treatment with H(2). Copyright (c) 2009 Elsevier Ltd. All rights reserved.

  4. Photocatalytic reduction of Cr(VI) by char/TiO2 composite photocatalyst: optimization and modeling using the response surface methodology (RSM).

    Science.gov (United States)

    Antonopoulou, M; Chondrodimou, I; Bairamis, F; Giannakas, A; Konstantinou, I

    2017-01-01

    The photocatalytic reduction of Cr(VI) using pyrolytic char/TiO2 (PC/TiO2) composite catalyst under simulated solar irradiation was studied. Response surface methodology (RSM) and experimental design were used for modeling the removal kinetics and for the optimization of operational parameters. RSM was developed by considering a central composite design with four input variable, i.e. catalyst concentration, initial concentration of Cr(VI), pH, and % (v/v) methanol concentration for assessing individual and interactive effects. A quadratic model was established as a functional relationship between four independent variables and the removal efficiency of Cr(VI). It was found that all selected variables have significant effect on Cr(VI) removal efficiency; however, the pH, the % concentration of methanol, and their interaction exhibited the major effects. Within the studied experimental ranges, the optimum conditions for maximum Cr(VI) removal efficiency (72.1 %) after 60 min of photocatalytic treatment were: catalyst concentration 55 mg L-1, Cr(VI) concentration 20 mg L-1, pH 4, and 5 % (v/v) methanol concentration. Under optimum conditions, Cr(VI) reductive removal followed pseudo-first-order kinetics, and nearly complete removal took place within 90 min. The results revealed the feasibility and the effectiveness of PC/TiO2 as photocatalyst in reduction reactions due to their ability of e--h+ pair separation increasing the transfer of the photogenerated e- to the catalyst's surface and thus the reduction of Cr(VI).

  5. MIL-53(Fe) as a highly efficient bifunctional photocatalyst for the simultaneous reduction of Cr(VI) and oxidation of dyes

    Energy Technology Data Exchange (ETDEWEB)

    Liang, Ruowen; Jing, Fenfen; Shen, Lijuan; Qin, Na; Wu, Ling, E-mail: wuling@fzu.edu.cn

    2015-04-28

    Highlights: • Fe(III)-based MOF was firstly applied to the photocatalytic reduction reaction. • MIL-53(Fe) exhibited an outstanding photocatalytic activity for reduction of Cr(VI). • A first systematic study of the Fe(III)-based MOF as bifunctional photocatalyst. • Dyes and Cr(VI) could be also converted simultaneously over MIL-53(Fe). • MIL-53(Fe) was performed a stable and reusable visible-light-driven photocatalyst. - Abstract: A bifunctional photocatalyst-Fe-benzenedicarboxylate (MIL-53(Fe)) has been synthesized successfully via a facile solvothermal method. The resulting MIL-53(Fe) photocatalyst exhibited an excellent visible light (λ ≥ 420 nm) photocatalytic activity for the reduction of Cr(VI), the reduction rate have reached about 100% after 40 min of visible light irradiation, which has been more efficient than that of N-doped TiO{sub 2} (85%) under identical experimental conditions. Further experimental results have revealed that the photocatalytic activity of MIL-53(Fe) for the reduction of Cr(VI) can be drastically affected by the pH value of the reaction solution, the hole scavenger and atmosphere. Moreover, MIL-53(Fe) has exhibited considerable photocatalytic activity in the mixed systems (Cr(VI)/dyes). After 6 h of visible light illumination, the reduction ratio of Cr(VI) and the degradation ratio of dyes have been exceed 60% and 80%, respectively. More significantly, the synergistic effect can also be found during the process of photocatalytic treatment of Cr(VI) contained wastewater under the same photocatalytic reaction conditions, which makes it a potential candidate for environmental restoration. Finally, a possible reaction mechanism has also been investigated in detail.

  6. Sulfur-Doped Carbon Nitride Polymers for Photocatalytic Degradation of Organic Pollutant and Reduction of Cr(VI).

    Science.gov (United States)

    Zheng, Yun; Yu, Zihao; Lin, Feng; Guo, Fangsong; Alamry, Khalid A; Taib, Layla A; Asiri, Abdullah M; Wang, Xinchen

    2017-04-01

    As a promising conjugated polymer, binary carbon nitride has attracted extensive attention as a metal-free and visible-light-responsive photocatalyst in the area of photon-involving purification of water and air. Herein, we report sulfur-doped polymeric carbon nitride microrods that are synthesized through thermal polymerization based on trithiocyanuric acid and melamine (TM) supramolecular aggregates. By tuning the polymerization temperature, a series of sulfur-doped carbon nitride microrods are prepared. The degradation of Rhodamine B (RhB) and the reduction of hexavalent chromium Cr(VI) are selected as probe reactions to evaluate the photocatalytic activities. Results show that increasing pyrolysis temperature leads to a large specific surface area, strong visible-light absorption, and accelerated electron-hole separation. Compared to bulk carbon nitride, the highly porous sulfur-doped carbon nitride microrods fabricated at 650 °C exhibit remarkably higher photocatalytic activity for degradation of RhB and reduction of Cr(VI). This work highlights the importance of self-assembly approach and temperature-control strategy in the synthesis of photoactive materials for environmental remediation.

  7. Cr(VI) photocatalytic reduction: Effects of simultaneous organics oxidation and of gold nanoparticles photodeposition on TiO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Dozzi, Maria Vittoria; Saccomanni, Alessia [Dipartimento di Chimica Fisica ed Elettrochimica and CIMAINA, Universita degli Studi di Milano, via Golgi 19, I-20133 Milano (Italy); Selli, Elena, E-mail: elena.selli@unimi.it [Dipartimento di Chimica Fisica ed Elettrochimica and CIMAINA, Universita degli Studi di Milano, via Golgi 19, I-20133 Milano (Italy)

    2012-04-15

    Highlights: Black-Right-Pointing-Pointer The Cr(VI) photocatalytic reduction rate is limited by the charge separation efficiency. Black-Right-Pointing-Pointer In the presence of hole scavengers, the reaction rate increases with adsorption. Black-Right-Pointing-Pointer Direct or indirect hole scavengers differently affect Cr(VI) photoreduction on TiO{sub 2}. Black-Right-Pointing-Pointer Au nanoparticles deposition on TiO{sub 2} has scarce effect on photocatalytic reactions. Black-Right-Pointing-Pointer The Au photodeposition treatment affects TiO{sub 2} surface properties and photoactivity. - Abstract: Commercial TiO{sub 2} samples with different phase composition and surface area were tested as photocatalysts in the photoinduced reduction of Cr(VI) in aqueous suspensions at pH 3.7 under UV-visible light irradiation. This reaction was also coupled with the simultaneous photocatalytic oxidation of the pollutant azo dye Acid Orange 8 (AO8) and of formic acid, acting as hole scavengers. The co-presence of oxidizable and reducible species ensured better separation of photogenerated charge carriers, resulting in a higher rate of both organics' oxidation and Cr(VI) reduction, especially in the case of high surface area anatase TiO{sub 2}, having the strongest affinity for Cr(VI) and AO8, as demonstrated by competitive adsorption tests. The effects on Cr(VI) photocatalytic reduction of gold nanoparticles photodeposited on TiO{sub 2} and of the Au loading were also investigated, aiming at ascertaining if this noble metal plays a role in the electron transfer processes involved in Cr(VI) reduction.

  8. Impact of Fe(III) as an effective electron-shuttle mediator for enhanced Cr(VI) reduction in microbial fuel cells: Reduction of diffusional resistances and cathode overpotentials.

    Science.gov (United States)

    Wang, Qiang; Huang, Liping; Pan, Yuzhen; Quan, Xie; Li Puma, Gianluca

    2017-01-05

    The role of Fe(III) was investigated as an electron-shuttle mediator to enhance the reduction rate of the toxic heavy metal hexavalent chromium (Cr(VI)) in wastewaters, using microbial fuel cells (MFCs). The direct reduction of chromate (CrO4(-)) and dichromate (Cr2O7(2-)) anions in MFCs was hampered by the electrical repulsion between the negatively charged cathode and Cr(VI) functional groups. In contrast, in the presence of Fe(III), the conversion of Cr(VI) and the cathodic coulombic efficiency in the MFCs were 65.6% and 81.7%, respectively, 1.6 times and 1.4 folds as those recorded in the absence of Fe(III). Multiple analytical approaches, including linear sweep voltammetry, Tafel plot, cyclic voltammetry, electrochemical impedance spectroscopy and kinetic calculations demonstrated that the complete reduction of Cr(VI) occurred through an indirect mechanism mediated by Fe(III). The direct reduction of Cr(VI) with cathode electrons in the presence of Fe(III) was insignificant. Fe(III) played a critical role in decreasing both the diffusional resistance of Cr(VI) species and the overpotential for Cr(VI) reduction. This study demonstrated that the reduction of Cr(VI) in MFCs was effective in the presence of Fe(III), providing an alternative and environmentally benign approach for efficient remediation of Cr(VI) contaminated sites with simultaneous production of renewable energy. Copyright © 2016 Elsevier B.V. All rights reserved.

  9. In Situ Spectral Kinetics of Cr(VI) Reduction by c-Type Cytochromes in A Suspension of Living Shewanella putrefaciens 200

    Science.gov (United States)

    Liu, Tongxu; Li, Xiaomin; Li, Fangbai; Han, Rui; Wu, Yundang; Yuan, Xiu; Wang, Ying

    2016-07-01

    Although c-type cytochromes (c-Cyts) mediating metal reduction have been mainly investigated with in vitro purified proteins of dissimilatory metal reducing bacteria, the in vivo behavior of c-Cyts is still unclear given the difficulty in measuring the proteins of intact cells. Here, c-Cyts in living Shewanella putrefaciens 200 (SP200) was successfully quantified using diffuse-transmission UV/Vis spectroscopy due to the strong absorbance of hemes, and the in situ spectral kinetics of Cr(VI) reduction by c-Cyts were examined over time. The reduced product Cr(III) observed on the cell surface may play a role in inhibiting the Cr(VI) reduction and reducing the cell numbers with high concentrations (>200 μM) of Cr(VI) evidenced by the 16S rRNA analysis. A brief kinetic model was established with two predominant reactions, redox transformation of c-Cyts and Cr(VI) reduction by reduced c-Cyts, but the fitting curves were not well-matched with c-Cyts data. The Cr(III)-induced inhibitory effect to the cellular function of redox transformation of c-Cyts was then added to the model, resulting in substantially improved the model fitting. This study provides a case of directly examining the reaction properties of outer-membrane enzyme during microbial metal reduction processes under physiological conditions.

  10. MIL-53(Fe) as a highly efficient bifunctional photocatalyst for the simultaneous reduction of Cr(VI) and oxidation of dyes.

    Science.gov (United States)

    Liang, Ruowen; Jing, Fenfen; Shen, Lijuan; Qin, Na; Wu, Ling

    2015-04-28

    A bifunctional photocatalyst-Fe-benzenedicarboxylate (MIL-53(Fe)) has been synthesized successfully via a facile solvothermal method. The resulting MIL-53(Fe) photocatalyst exhibited an excellent visible light (λ≥ 420nm) photocatalytic activity for the reduction of Cr(VI), the reduction rate have reached about 100% after 40min of visible light irradiation, which has been more efficient than that of N-doped TiO2 (85%) under identical experimental conditions. Further experimental results have revealed that the photocatalytic activity of MIL-53(Fe) for the reduction of Cr(VI) can be drastically affected by the pH value of the reaction solution, the hole scavenger and atmosphere. Moreover, MIL-53(Fe) has exhibited considerable photocatalytic activity in the mixed systems (Cr(VI)/dyes). After 6h of visible light illumination, the reduction ratio of Cr(VI) and the degradation ratio of dyes have been exceed 60% and 80%, respectively. More significantly, the synergistic effect can also be found during the process of photocatalytic treatment of Cr(VI) contained wastewater under the same photocatalytic reaction conditions, which makes it a potential candidate for environmental restoration. Finally, a possible reaction mechanism has also been investigated in detail. Copyright © 2015 Elsevier B.V. All rights reserved.

  11. Carbon quantum dots decorated MoSe2 photocatalyst for Cr(VI) reduction in the UV-vis-NIR photon energy range.

    Science.gov (United States)

    Ren, Zhenxing; Liu, Xinjuan; Chu, Haipeng; Yu, Huangze; Xu, Yuanyuan; Zheng, Wei; Lei, Wenyan; Chen, Pengbin; Li, Jianwei; Li, Can

    2017-02-15

    Developing whole spectrum responsive photocatalysts is one of greatly significant subjects from the viewpoint of using solar energy. Here we have firstly developed a carbon quantum dots-decorated MoSe2 photocatalyst that is active in the whole spectrum of solar light for Cr(VI) reduction. The Cr(VI) reduction rate of higher than 99% has been achieved with 1wt.% nanocarbon emersions under UV, visible and near-infrared irradiation at 180min. Improvement is attributed to its excellent light absorption, efficient charge separation, and the light down converting effect of carbon quantum dots. Copyright © 2016 Elsevier Inc. All rights reserved.

  12. Simulated solarlight catalytic reduction of Cr(VI) on microwave–ultrasonication synthesized flower-like CuO in the presence of tartaric acid

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Zhihui [College of Science, Nanjing Agricultural University, Nanjing 210095 (China); Yu, Yaqun; Fang, Di; Liang, Jianru [College of Resources and Environmental Science, Nanjing Agricultural University, Nanjing 210095 (China); Zhou, Lixiang, E-mail: lxzhou@njau.edu.cn [College of Resources and Environmental Science, Nanjing Agricultural University, Nanjing 210095 (China)

    2016-03-01

    In this study, flower-like CuO was successfully synthesized by a microwave–ultrasound assisted method and well characterized by X-ray diffractions, Fourier transform infrared spectrum, scanning electron microscopy, transmission electron microscopy, specific surface area, UV–vis diffused reflection spectra, X-ray photoelectron spectroscopy and point of zero charge. The photocatalytic performance of the as-prepared CuO was examined on the Cr(VI) reduction in the presence of tartaric acid under simulated solarlight irradiation. The results show that the developed CuO catalyst exhibited good photocatalytic activity with 100% reduction of Cr(VI) after irradiation of 30 min under the test condition of c(Cr(VI)) = 100 μM, catalyst loading = 400 mg/L, c(tartaric acid) = 4 mM and initial pH = 3. The reaction mechanism was proposed. The effects of test parameters, such as catalyst loading, tartaric acid concentration and initial pH, on Cr(VI) reduction efficiency were also investigated. It is worth mentioning that the developed catalyst can work at a relatively wide range of pH with quite high catalytic performance. - Highlights: • Flower-like CuO microstructure was prepared by MW-US assisted method. • The prepared CuO can catalyze the reduction Cr(VI) by tartaric acid under simulated solarlight. • The formation of ≡Cu(II)-tartaric acid complex play a key role in the reduction of Cr(VI). • The catalyst can operate effectively at a relatively wide range of pH.

  13. Bi25VO40 microcube with step surface for visible light photocatalytic reduction of Cr(VI): Enhanced activity and ultrasound assisted regeneration.

    Science.gov (United States)

    Wang, Pei; Ji, Wenda; Li, Mingmeng; Zhang, Gaoke; Wang, Jinlong

    2017-09-01

    In this study, a kind of bismuth vanadium (Bi25VO40) microcube with step surface was successfully synthesized by a fast and mild hydrothermal method. The reaction time and hydrothermal temperature are the key factors which are accounted for the formation of this unique structure. The as-prepared Bi25VO40 microcube exhibited considerably higher visible light photocatalytic activity compared with the smooth one, revealing that fabrication of Bi25VO40 with step surface was an effective method to improve the photocatalytic activity. The enhanced photocatalytic activity over this Bi25VO40 could be attributed to its enhanced separation efficiency of photo-generated holes and electrons. In addition, the XPS analysis of the Bi25VO40 after photo-reduction showed that most of highly toxic Cr(VI) were reduced into less dangerous Cr(III). The XRD results indicated the reduced Cr(III) existed in the form of Cr2O3 and Cr3O8 on the catalyst surface and occupied the active site, counting for the decreased activity after multiple use. A facile ultrasound treatment facilitated the regeneration of deactivated photocatalyst by removing the adsorbed Cr2O3 and Cr3O8, improving the removal ratio of Cr(VI) over the photocatalyst from 74.0% to 85.6% after four recycling use, which make it applicable for the photocatalytic removal of a typical Cr(VI) pollutant continuously. Copyright © 2017 Elsevier B.V. All rights reserved.

  14. Remediation of Cr(VI) in solution using vitamin C*

    OpenAIRE

    LIU, Yong; Xu, Xin-hua; He, Ping

    2005-01-01

    The effectiveness of vitamin C in treating Cr(VI)-contaminated water is being evaluated. Cr(VI) is an identified pollutant of some soils and groundwater. Vitamin C, an important biological reductant in humans and animals, can be used to transform Cr(VI) to essentially nontoxic Cr(III). The removal efficiency was 89% when the mass concentration of vitamin C was 80 mg/L in 60 min, and nearly 100% Cr(VI) was removed when the mass concentration was 100 mg/L. Our data demonstrated that the removal...

  15. Kinetics of Cr(III) and Cr(VI) removal from water by two floating macrophytes.

    Science.gov (United States)

    Maine, M A; Hadad, H R; Sánchez, G; Caffaratti, S; Pedro, M C

    2016-01-01

    The aim of this work was to compare Cr(III) and Cr(VI) removal kinetics from water by Pistia stratiotes and Salvinia herzogii. The accumulation in plant tissues and the effects of both Cr forms on plant growth were also evaluated. Plants were exposed to 2 and 6 mg L(-1) of Cr(III) or Cr(VI) during 30 days. At the end of the experiment, Cr(VI) removal percentages were significantly lower than those obtained for Cr(III) for both macrophytes. Cr(III) removal kinetics involved a fast and a slow component. The fast component was primarily responsible for Cr(III) removal while Cr(VI) removal kinetics involved only a slow process. Cr accumulated principally in the roots. In the Cr(VI) treatments a higher translocation from roots to aerial parts than in Cr(III) treatments was observed. Both macrophytes demonstrated a high ability to remove Cr(III) but not Cr(VI). Cr(III) inhibited the growth at the highest studied concentration of both macrophytes while Cr(VI) caused senescence. These results have important implications in the use of constructed wetlands for secondary industrial wastewater treatment. Common primary treatments of effluents containing Cr(VI) consists in its reduction to Cr(III). Cr(III) concentrations in these effluents are normally below the highest studied concentrations in this work.

  16. Facile synthesis of amino-functionalized titanium metal-organic frameworks and their superior visible-light photocatalytic activity for Cr(VI) reduction

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Hou [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environment Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Yuan, Xingzhong, E-mail: yxz@hnu.edu.cn [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environment Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Wu, Yan [College of Environment and Energy, South China University of Technology, Guangzhou 510006 (China); Zeng, Guangming [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environment Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Chen, Xiaohong [School of Business, Central South University, Changsha 410083 (China); Leng, Lijian; Wu, Zhibin; Jiang, Longbo [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environment Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Li, Hui [Institute of Bio-energy, Hunan Academy of Forestry, Changsha 410004 (China)

    2015-04-09

    Highlights: • NH{sub 2} functionalized MIL-125(Ti) was fabricated by a facile solvothermal method. • The photocatalyst could reduce Cr(VI)–Cr(III) under visible light irradiation. • The Ti{sup 3+}–Ti{sup 4+} intervalence electron transfer is important for Cr(VI) reduction. • Used NH{sub 2}-MIL-125(Ti) can be recycled for the photocatalytic reduction. - Abstract: Porous metal-organic frameworks (MOFs) have been arousing a great interest in exploring the application of MOFs as photocatalyst in environment remediation. In this work, two different MOFs, Ti-benzenedicarboxylate (MIL-125(Ti)) and amino-functionalized Ti-benzenedicarboxylate (NH{sub 2}-MIL-125(Ti)) were successfully synthesized via a facile solvothermal method. The MIL-125(Ti) and NH{sub 2}-MIL-125(Ti) were well characterized by XRD, SEM, XPS, N{sub 2} adsorption–desorption measurements, thermogravimetric analysis and UV–vis diffuse reflectance spectra (DRS). It is revealed that the NH{sub 2}-MIL-125(Ti) has well crystalline lattice, large surface area and mesoporous structure, chemical and thermal stability, and enhanced visible-light absorption up to 520 nm, which was associated with the chromophore (amino group) in the organic linker. Compared with MIL-125(Ti), NH{sub 2}-MIL-125(Ti) exhibited more efficient photocatalytic activity for Cr(VI) reduction from aqueous solution under visible-light irradiation. The addition of hole scavenger, the hole scavenger concentration and the pH value of the reaction solution played important roles in the photo-catalytic reduction of Cr(VI). The presence of Ti{sup 3+}–Ti{sup 4+} intervalence electron transfer was the main reason for photo-excited electrons transportation from titanium-oxo clusters to Cr(VI), facilitating the Cr(VI) reduction under the acid condition. It was demonstrated that amino-functionalized Ti(IV)-based MOFs could be promising visible-light photocatalysts for the treatment of Cr(VI)-contained wastewater.

  17. Field and Numerical Modeling Study of Reductive Bioimmobilization of Cr (VI) in Groundwater at Hanford 100-H Site

    Science.gov (United States)

    Hazen, T. C.; Sonnenthal, E. L.; Mukhopadhyay, S.; Steefel, C. I.; Long, P. E.; Faybishenko, B.

    2009-12-01

    The 2004-2008 field experiment at the Hanford 100-H Site showed that a single injection of the hydrogen release compound (HRC)—a mixture of slow release glycerol polylactate, fast disassociating lactic acid, and glycerol into groundwater— stimulated an increase in biomass and a depletion of terminal electron acceptors, resulting in a significant decrease in soluble Cr (VI). The Cr (VI) concentration remained below the background concentration in the downgradient pumping/monitoring well, and below the detection limit in the injection well, for more than 3 years after the initial HRC injection in 2004. Reaction-transport modeling of the field experiment was performed to elucidate reaction pathways and rates of biogeochemical processes governing Cr (VI) bioimmobilization. Field observation data were used to develop a 3-D hydraulic and reaction-transport-isotopic model, simulated using the TOUGHREACT code. This model was used to assess the degradation kinetics of the HRC, the effects of lactate and acetate-induced bioreduction of Cr and Fe, and the effects on Cr and Sr isotopic compositions in the fluids and mineral phases (calcite dissolution in the acidic plume and precipitation at the fringes). The 2008 experiment involved reinjection of HRC into the same zones as the earlier injection and likely resulted in dissolution of previously precipitated Cr (Fe) hydroxides and additional calcite dissolution in sediments outside of the wellbore. Detailed results of the integrated field and modeling study will be presented.

  18. Cr(VI) reduction into Cr(III) as a mechanism to explain the low sensitivity of Vibrio fischeri bioassay to detect chromium pollution.

    Science.gov (United States)

    Fulladosa, Elena; Desjardin, Valérie; Murat, Jean-Claude; Gourdon, Rémy; Villaescusa, Isabel

    2006-10-01

    Vibrio fischeri bacteria, used as a biological target in either acute or chronic toxicity tests, display a low sensitivity to Cr(VI). This phenomenon could be due to the capacity of these bacteria to reduce Cr(VI) into Cr(III). This reducing capacity was found to depend on culture medium composition, pH value, incubation time and the presence of a carbon source. It also depends on the nature of the carbon source, glucose being more efficient than glycerol. This is probably related to differences in bacterial metabolism when given either glucose or glycerol. The thermostable Cr(VI)-reducing activity found in the supernatants of V. fischeri cultures grown on glucose suggests that, under these conditions, the bacteria release non-proteic reducing substances which have not been identified yet.

  19. Efficient photocatalytic reduction of aqueous Cr(VI) over flower-like SnIn{sub 4}S{sub 8} microspheres under visible light illumination

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Lin [Key Laboratory of Industrial Ecology and Environmental Engineering (MOE) and State Key Laboratory of Fine Chemical, School of Environmental Science and Technology, Dalian University of Technology, Dalian 116024 (China); Li, Xinyong, E-mail: xyli@dlut.edu.cn [Key Laboratory of Industrial Ecology and Environmental Engineering (MOE) and State Key Laboratory of Fine Chemical, School of Environmental Science and Technology, Dalian University of Technology, Dalian 116024 (China); Department of Chemical and Biomolecular Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon (Hong Kong); Teng, Wei; Zhao, Qidong; Shi, Yong [Key Laboratory of Industrial Ecology and Environmental Engineering (MOE) and State Key Laboratory of Fine Chemical, School of Environmental Science and Technology, Dalian University of Technology, Dalian 116024 (China); Yue, Renliang [State Key Laboratory of Multi-Phase Complex Systems, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190 (China); Chen, Yunfa, E-mail: yfchen@home.ipe.ac.cn [State Key Laboratory of Multi-Phase Complex Systems, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190 (China)

    2013-01-15

    Highlights: ► SnIn{sub 4}S{sub 8} was used in photocatalytic reduction of aqueous Cr(VI) for the first time. ► Flower-like SnIn{sub 4}S{sub 8} microspheres with numerous uniform pores were fabricated. ► High visible light photocatalytic activity and good photocatalytic stability. -- Abstract: Photocatalytic reduction of aqueous Cr(VI) was successfully achieved on nanostructured SnIn{sub 4}S{sub 8}. The SnIn{sub 4}S{sub 8} particles with flower-like nanostructure were synthesized via a facile solvothermal method. UV–vis diffuse reflectance spectra (DRS) indicated that the SnIn{sub 4}S{sub 8} particles had strong absorption in visible region and the band gap was estimated to be from 2.27 to 2.35 eV. The photocatalytic reduction of aqueous Cr(VI) by flower-like SnIn{sub 4}S{sub 8} was evaluated under visible light (λ > 400 nm) irradiation. The polyvinyl pyrrolidone (PVP) assisted SnIn{sub 4}S{sub 8} sample exhibits excellent removal efficiency of Cr(VI) (∼97%) and good photocatalytic stability. The predominant photocatalytic activity is due to its large surface area, strong absorption in visible-light region and excellent charge separation characteristics.

  20. Synergistic photocatalysis of Cr(VI) reduction and 4-Chlorophenol degradation over hydroxylated α-Fe{sub 2}O{sub 3} under visible light irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Ji-Chao; Ren, Juan [College of Chemistry and Molecular Engineering, Zhengzhou University, Zhengzhou 450002 (China); Yao, Hong-Chang, E-mail: yaohongchang@zzu.edu.cn [College of Chemistry and Molecular Engineering, Zhengzhou University, Zhengzhou 450002 (China); Zhang, Lin; Wang, Jian-She; Zang, Shuang-Quan [College of Chemistry and Molecular Engineering, Zhengzhou University, Zhengzhou 450002 (China); Han, Li-Feng [Henan Provincial Key Laboratory of Surface & Interface Science, Zhengzhou University of Light Industry, Zhengzhou 450002 (China); Li, Zhong-Jun, E-mail: lizhongjun@zzu.edu.cn [College of Chemistry and Molecular Engineering, Zhengzhou University, Zhengzhou 450002 (China)

    2016-07-05

    Highlights: • The surface hydroxyl of Fe{sub 2}O{sub 3} influences on the Cr(VI) reduction activity. • The synergistic photocatalysis enhances degradation activity of Cr(VI) and 4-CP. • The Fe{sub 2}O{sub 3} catalyst exhibits good stability and degradation activity after 9 runs. - Abstract: A series of Fe{sub 2}O{sub 3} materials with hydroxyl are synthesized in different monohydric alcohol (C{sub 2} – C{sub 5}) solvents by solvothermal method and characterized by XRD, BET, XPS, TG and EA. The amount of hydroxyl is demonstrated to be emerged on the surface of the as-synthesized Fe{sub 2}O{sub 3} particles and their contents are determined to be from 7.99 to 3.74 wt%. The Cr(VI) reduction experiments show that the hydroxyl content of Fe{sub 2}O{sub 3} samples exacts great influence on the photocatalytic activity under visible light irradiation (λ > 400 nm) and that the Fe{sub 2}O{sub 3} sample synthesized in n-butyl alcohol exhibits the optimal photocatalytic activity. The synergistic photocatalysis for 4-Chlorophenol (4-CP) degradation and Cr(VI) reduction over above Fe{sub 2}O{sub 3} sample is further investigated. The photocatalytic ratio of Cr(VI) reduction are enhanced from 24.8% to 70.2% while that of 4-CP oxidation are increased from 13.5% to 47.8% after 1 h visible light irradiation. The Fe{sub 2}O{sub 3} sample keeps good degradation rates of mixed pollutants after 9 runs. The active oxygen intermediates O{sub 2}{sup −}·, ·OH and H{sub 2}O{sub 2} formed in the photoreaction process are discovered by ESR measurement and UV–vis test. The photocatalytic degradation mechanism is proposed accordingly.

  1. Cr(VI) reduction and immobilization by novel carbonaceous modified magnetic Fe{sub 3}O{sub 4}/halloysite nanohybrid

    Energy Technology Data Exchange (ETDEWEB)

    Tian, Xike, E-mail: xktian@cug.edu.cn [Faculty of Material Science and Chemistry, China University of Geosciences, Wuhan 430074 (China); Wang, Weiwei; Tian, Na; Zhou, Chaoxin; Yang, Chao [Faculty of Material Science and Chemistry, China University of Geosciences, Wuhan 430074 (China); Komarneni, Sridhar [Materials Research Laboratory, Materials Research Institute and Department of Ecosystem Science and Management, The Pennsylvania State University, University Park, PA 16802 (United States)

    2016-05-15

    Highlights: • A novel magnetic nonohybrids (Fe{sub 3}O{sub 4}/HNTs@C) were synthesized for Cr(VI) removal. • Cr(VI) was reduced to Cr(III) by Fe{sub 3}O{sub 4} nanoparticles and hydroxyl groups. • Cr ions were attached on Fe{sub 3}O{sub 4}/HNTs@C by ion exchange and coordination interaction. - Abstract: In this work, a novel “Dumbbell-like” magnetic Fe{sub 3}O{sub 4}/Halloysite nanohybrid (Fe{sub 3}O{sub 4}/HNTs@C) with oxygen-containing organic group grafting on the surface of natural halloysite nanotubes (HNTs) and homogeneous Fe{sub 3}O{sub 4} nanospheres selectively aggregating at the tips of modified halloysite nanotubes was successfully synthesized. XRD, TEM, IR spectroscopy, XPS and VSM were used to characterize this newly halloysite nanohybrid and its formation mechanism was discussed. Cr(VI) ions adsorption experiments showed that the Fe{sub 3}O{sub 4}/halloysite nanohybrid exhibited higher adsorption ability with a maximum adsorption capacity of 132 mg/L at 303 K, which is about 100 times higher than that of unmodified halloysite nanotubes. More importantly, with the reduction of Fe{sub 3}O{sub 4} and electron–donor effect of oxygen-containing organic groups, Cr(VI) ions were easily reduced into low toxicity Cr(III) and then adsorbed onto the surface of halloysite nanohybrid. In addition, appreciable magnetization was observed due to the aggregation of magnetite nanoparticles, which make adsorbent facility separated from aqueous solutions after Cr pollution adsorption.

  2. CdS sensitized TiO{sub 2} film for photocatalytic reduction of Cr(VI) by microwave-assisted chemical bath deposition method

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Xinjuan; Pan, Likun, E-mail: lkpan@phy.ecnu.edu.cn; Lv, Tian; Sun, Zhuo

    2014-01-15

    Highlights: • CdS sensitized TiO{sub 2} films are synthesized by microwave-assisted deposition method. • The photocatalytic reduction of Cr(VI) by CdS sensitized TiO{sub 2} film is investigated. • A high Cr(VI) reduction rate of 93% is achieved under white LED light irradiation. -- Abstract: CdS quantum dots (QDs) sensitized TiO{sub 2} films were successfully synthesized using one-step microwave assisted chemical bath deposition method, which allows a facile and rapid deposition and integration between CdS QDs and TiO{sub 2} films. The photocatalytic performance of the films fabricated using CdS precursor solutions with different concentrations in the reduction of Cr(VI) under white light emitting diode (LED) light irradiation was investigated. The results show that the CdS sensitization can enhance the photocatalytic performance of TiO{sub 2} film with a maximum reduction rate of 93% for 240 min under white LED light irradiation as compared with the pure TiO{sub 2} film (31%) due to the increase of light absorption and the reduction of recombination of the injected electrons from CdS to TiO{sub 2}.

  3. Facile synthesis of porous single crystalline ZnO nanoplates and their application in photocatalytic reduction of Cr(VI) in the presence of phenol

    Energy Technology Data Exchange (ETDEWEB)

    Jin, Zhen [Research Center for Biomimetic Functional Materials and Sensing Devices, Institute of Intelligent Machines, Chinese Academy of Sciences, Hefei, Anhui 230031 (China); Zhang, Yong-Xing [School of Physics and Electronic Information, Huaibei Normal University, Huaibei, Anhui 235000 (China); Meng, Fan-Li; Jia, Yong; Luo, Tao; Yu, Xin-Yao; Wang, Jin; Liu, Jin-Huai [Research Center for Biomimetic Functional Materials and Sensing Devices, Institute of Intelligent Machines, Chinese Academy of Sciences, Hefei, Anhui 230031 (China); Huang, Xing-Jiu, E-mail: xingjiuhuang@iim.ac.cn [Research Center for Biomimetic Functional Materials and Sensing Devices, Institute of Intelligent Machines, Chinese Academy of Sciences, Hefei, Anhui 230031 (China)

    2014-07-15

    Graphical abstract: - Highlights: • Porous single crystalline ZnO nanoplates were successfully synthesized. • The nanoplates were with 12 nm in thickness and tens nanometers in pore size. • A synergistic effect of enhanced Cr(VI) photoreduction and phenol degradation was observed. • A possible reaction mechanism was discussed. - Abstract: Porous single crystalline ZnO nanoplates were successfully synthesized through a facile and cost-effective hydrothermal process at low temperature condition, followed by annealing of the zinc carbonate hydroxide hydrate precursors. The as-prepared products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Brunauer–Emmett–Teller (BET) measurements. The porous single crystalline ZnO nanoplates are with 12 nm thickness and pore ranging from 10 nm to several tens of nanometers. The porous structure of the ZnO nanoplates caused large amount of surface defects which worked as photogenerated holes’ shallow trappers and largely restrained the recombination of photogenerated electrons and holes, resulting in a significantly high photocatalytic activity and durability toward the photoreduction of Cr(VI) under UV irradiation. Moreover, a synergistic effect, that is, increased photocatalytic reduction of Cr(VI) and degradation of phenol, can be observed. Furthermore, the synergistic photocatalytic mechanism has also been discussed. Those results present an enlightenment to employ porous single crystalline nanomaterials to remove Cr(VI) and organic pollutants simultaneously.

  4. The reactivity of Fe(II) associated with goethite formed during short redox cycles toward Cr(VI) reduction under oxic conditions

    Energy Technology Data Exchange (ETDEWEB)

    Tomaszewski, Elizabeth J.; Lee, Seungyeol; Rudolph, Jared; Xu, Huifang; Ginder-Vogel, Matthew (UW)

    2017-08-01

    Chromium (Cr) is a toxic metal that causes a myriad of health problems and enters the environment as a result of anthropogenic activities and/or natural processes. The toxicity and solubility of chromium is linked to its oxidation state; Cr(III) is poorly soluble and relatively nontoxic, while Cr(VI) is soluble and a known carcinogen. Solid Fe(II) in iron-bearing minerals, such as pyrite, magnetite, and green rusts, reduce the oxidation state of chromium, reducing its toxicity and mobility. However, these minerals are not the only potential sources of solid-associated Fe(II) available for Cr(VI) reduction. For example, ferric (Fe(III)) (hydr)oxides, such as goethite or hematite, can have Fe(II) in the solid without phase transformation; however, the reactivity of Fe(II) within Fe(III) (hydr)oxides with contaminants, has not been previously investigated. Here, we cyclically react goethite with dissolved Fe(II) followed by dissolved O2, leading to the formation of reactive Fe(II) associated with goethite. In separate reactors, the reactivity of this Fe(II) is probed under oxic conditions, by exposure to chromate (CrO42 -) after either one, two, three or four redox cycles. Cr is not present during redox cycling; rather, it is introduced to a subset of the solid after each oxidation half-cycle. Analysis of X-ray absorption near edge structure (XANES) spectra reveals that the extent of Cr(VI) reduction to Cr(III) depends not only on solid Fe(II) content but also surface area and mean size of ordered crystalline domains, determined by BET surface area analysis and X-ray diffraction (XRD), respectively. Shell-by-shell fitting of the extended X-ray absorption fine structure (EXAFS) spectra demonstrates chromium forms both single and double corner sharing complexes on the surface of goethite, in addition to sorbed Cr(III) species. Finally, transmission electron microscope (TEM) imaging and X-ray energy-dispersive spectroscopy (EDS) illustrate that Cr preferentially

  5. Facile synthesis of AgI/BiOI-Bi{sub 2}O{sub 3} multi-heterojunctions with high visible light activity for Cr(VI) reduction

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Qi [School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310018 (China); The Brook Byer Institute for Sustainable Systems and School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta 30332 (United States); Shi, Xiaodong; Liu, Enqin [School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310018 (China); Crittenden, John C. [The Brook Byer Institute for Sustainable Systems and School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta 30332 (United States); Ma, Xiangjuan; Zhang, Yi [School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310018 (China); Cong, Yanqing, E-mail: yqcong@hotmail.com [School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310018 (China)

    2016-11-05

    Graphical abstract: Highly visible-light-active AgI/BiOI-Bi{sub 2}O{sub 3} with multi-heterojunctions was developed. - Highlights: • Visible-light-active AgI/BiOI-Bi{sub 2}O{sub 3} with multi-heterojunctions was prepared. • Highly enhanced photocatalytic reduction of Cr(VI) was observed. • k{sub Cr(VI)} on AgI/BiOI-Bi{sub 2}O{sub 3} increased by ca.16 times relative to Bi{sub 2}O{sub 3}. • Decreased E{sub g}, shifted E{sub fb} and reduced charge transfer resistance were observed. • Simultaneous reduction of Cr(VI) and degradation of organics were achieved. - Abstract: AgI sensitized BiOI-Bi{sub 2}O{sub 3} composite (AgI/BiOI-Bi{sub 2}O{sub 3}) with multi-heterojunctions was prepared using simple etching-deposition process. Different characterization techniques were performed to investigate the structural, optical and electrical properties of the as-prepared photocatalysts. It was found that the ternary AgI/BiOI-Bi{sub 2}O{sub 3} composite exhibited: (1) improved photocurrent response, (2) smaller band gap, (3) greatly reduced charge transfer resistance and (4) negative shift of flat band potential, which finally led to easier generation and more efficient separation of photo-generated electron-hole pairs at the hetero-interfaces. Thus, for the reduction of Cr(VI), AgI/BiOI-Bi{sub 2}O{sub 3} exhibited excellent photocatalytic activity under visible light irradiation at near neutral pH. AgI/BiOI-Bi{sub 2}O{sub 3} was optimized when the initial molar ratio of KI to Bi{sub 2}O{sub 3} and AgNO{sub 3} to Bi{sub 2}O{sub 3} was 1:1 and 10%, respectively. The estimated k{sub Cr(VI)} on optimized AgI/BiOI-Bi{sub 2}O{sub 3} was about 16 times that on pure Bi{sub 2}O{sub 3}. Good stability was also observed in cyclic runs, indicating that the current multi-heterostructured photocatalyst is highly desirable for the remediation of Cr(VI)-containing wastewater.

  6. Synergistic photocatalysis of Cr(VI) reduction and 4-Chlorophenol degradation over hydroxylated α-Fe2O3 under visible light irradiation.

    Science.gov (United States)

    Wang, Ji-Chao; Ren, Juan; Yao, Hong-Chang; Zhang, Lin; Wang, Jian-She; Zang, Shuang-Quan; Han, Li-Feng; Li, Zhong-Jun

    2016-07-05

    A series of Fe2O3 materials with hydroxyl are synthesized in different monohydric alcohol (C2-C5) solvents by solvothermal method and characterized by XRD, BET, XPS, TG and EA. The amount of hydroxyl is demonstrated to be emerged on the surface of the as-synthesized Fe2O3 particles and their contents are determined to be from 7.99 to 3.74 wt%. The Cr(VI) reduction experiments show that the hydroxyl content of Fe2O3 samples exacts great influence on the photocatalytic activity under visible light irradiation (λ>400 nm) and that the Fe2O3 sample synthesized in n-butyl alcohol exhibits the optimal photocatalytic activity. The synergistic photocatalysis for 4-Chlorophenol (4-CP) degradation and Cr(VI) reduction over above Fe2O3 sample is further investigated. The photocatalytic ratio of Cr(VI) reduction are enhanced from 24.8% to 70.2% while that of 4-CP oxidation are increased from 13.5% to 47.8% after 1 h visible light irradiation. The Fe2O3 sample keeps good degradation rates of mixed pollutants after 9 runs. The active oxygen intermediates O2(-)˙, ˙OH and H2O2 formed in the photoreaction process are discovered by ESR measurement and UV-vis test. The photocatalytic degradation mechanism is proposed accordingly. Copyright © 2016 Elsevier B.V. All rights reserved.

  7. Facile synthesis of porous single crystalline ZnO nanoplates and their application in photocatalytic reduction of Cr(VI) in the presence of phenol.

    Science.gov (United States)

    Jin, Zhen; Zhang, Yong-Xing; Meng, Fan-Li; Jia, Yong; Luo, Tao; Yu, Xin-Yao; Wang, Jin; Liu, Jin-Huai; Huang, Xing-Jiu

    2014-07-15

    Porous single crystalline ZnO nanoplates were successfully synthesized through a facile and cost-effective hydrothermal process at low temperature condition, followed by annealing of the zinc carbonate hydroxide hydrate precursors. The as-prepared products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Brunauer-Emmett-Teller (BET) measurements. The porous single crystalline ZnO nanoplates are with 12nm thickness and pore ranging from 10nm to several tens of nanometers. The porous structure of the ZnO nanoplates caused large amount of surface defects which worked as photogenerated holes' shallow trappers and largely restrained the recombination of photogenerated electrons and holes, resulting in a significantly high photocatalytic activity and durability toward the photoreduction of Cr(VI) under UV irradiation. Moreover, a synergistic effect, that is, increased photocatalytic reduction of Cr(VI) and degradation of phenol, can be observed. Furthermore, the synergistic photocatalytic mechanism has also been discussed. Those results present an enlightenment to employ porous single crystalline nanomaterials to remove Cr(VI) and organic pollutants simultaneously. Copyright © 2014 Elsevier B.V. All rights reserved.

  8. Facile synthesis of AgI/BiOI-Bi2O3 multi-heterojunctions with high visible light activity for Cr(VI) reduction.

    Science.gov (United States)

    Wang, Qi; Shi, Xiaodong; Liu, Enqin; Crittenden, John C; Ma, Xiangjuan; Zhang, Yi; Cong, Yanqing

    2016-11-05

    AgI sensitized BiOI-Bi2O3 composite (AgI/BiOI-Bi2O3) with multi-heterojunctions was prepared using simple etching-deposition process. Different characterization techniques were performed to investigate the structural, optical and electrical properties of the as-prepared photocatalysts. It was found that the ternary AgI/BiOI-Bi2O3 composite exhibited: (1) improved photocurrent response, (2) smaller band gap, (3) greatly reduced charge transfer resistance and (4) negative shift of flat band potential, which finally led to easier generation and more efficient separation of photo-generated electron-hole pairs at the hetero-interfaces. Thus, for the reduction of Cr(VI), AgI/BiOI-Bi2O3 exhibited excellent photocatalytic activity under visible light irradiation at near neutral pH. AgI/BiOI-Bi2O3 was optimized when the initial molar ratio of KI to Bi2O3 and AgNO3 to Bi2O3 was 1:1 and 10%, respectively. The estimated kCr(VI) on optimized AgI/BiOI-Bi2O3 was about 16 times that on pure Bi2O3. Good stability was also observed in cyclic runs, indicating that the current multi-heterostructured photocatalyst is highly desirable for the remediation of Cr(VI)-containing wastewater. Copyright © 2016 Elsevier B.V. All rights reserved.

  9. Phosphomolybdate assembly as a low-cost catalyst for the reduction of toxic Cr(vi) in aqueous solution.

    Science.gov (United States)

    Wang, Xiaoxiao; Wang, Jiaojiao; Geng, Zongke; Qian, Zhao; Han, Zhangang

    2017-06-20

    Highly reduced phosphomolybdate hybrid compounds have been hydrothermally prepared and structurally defined. X-ray single-crystal analysis revealed that these phosphomolybdates had the following formulae: (H2bpp)6{Fe[Mo6O12(OH)3(HPO4)2(H2PO4)2]2}2·11H2O (1), (H2bpp)6{Zn[Mo6O12(OH)3(HPO4)2(H2PO4)2]2}2·11H2O (2), and (H2bpp)5.5{Mn[Mo6O12(OH)3(HPO4)2(H2PO4)2]2}2·2H2O (3) (bpp = 1,3-bi(4-pyridyl)propane). In the inorganic moiety, all Mo centers are in the +5 reduced form, representing a unique, fully reduced cluster in the polyanionic family. As a counter cation, the flexible bpp surrounds the anionic cluster to form hybrid 'core-shell' supramolecular assemblies. These hybrids are stable and insoluble in water, which can change a catalytic reaction from homogeneous to heterogeneous. Experiments showed that the three supramolecular hybrids exhibit ideally reversible multi-electron transfer behavior, and hybrid 1 is active as a heterogeneous molecular catalyst to reduce toxic Cr(vi) to nontoxic Cr(iii) at low temperature in a short period of time. Hybrid 1 serves as an electron shuttle to promote the redox reaction between Cr(vi) and HCOOH. The activation energy of the reaction is effectively decreased after the reactants are adsorbed on the solid crystal surface, and the activation energy is calculated to be 78.5 kJ·mol(-1). The well-organized structures of polyoxometalates help to explain the catalytic mechanism at the molecular level.

  10. Selective Reduction of Cr(VI) in Chromium, Copper and Arsenic (CCA) Mixed Waste Streams Using UV/TiO2 Photocatalysis

    OpenAIRE

    Shan Zheng; Wenjun Jiang; Mamun Rashid; Yong Cai; Dionysios D. Dionysiou; Kevin E. O'Shea

    2015-01-01

    The highly toxic Cr(VI) is a critical component in the Chromated Copper Arsenate (CCA) formulations extensively employed as wood preservatives. Remediation of CCA mixed waste and discarded treated wood products is a significant challenge. We demonstrate that UV/TiO2 photocatalysis effectively reduces Cr(VI) to less toxic Cr(III) in the presence of arsenate, As(V), and copper, Cu(II). The rapid conversion of Cr(VI) to Cr(III) during UV/TiO2 photocatalysis occurs over a range of concentrations,...

  11. Evaluation of the effects of various culture condition on Cr (VI)reduction by Shewanella oneidensis MR-1 in a novel high-throughputmini-bioreactor

    Energy Technology Data Exchange (ETDEWEB)

    Tang, Yinjie J.; Laidlaw, David; Gani, Kishen; Keasling, Jay D.

    2006-03-16

    The growth and Cr(VI) reduction by Shewanella oneidensisMR-1 was examined using a mini-bioreactor system that independentlymonitors and controls pH, dissolved oxygen, and temperature for each ofits 24, 10-mL reactors. Independent monitoring and control of eachreactor in the cassette allows the exploration of a matrix ofenvironmental conditions known to influence S. oneidensis chromiumreduction. S. oneidensis MR-1 grew in minimal medium without amino acidor vitamin supplementation under aerobic conditions but required serineand glycine supplementation under anaerobic conditions. Growth wasinhibited by dissolved oxygen concentrations>80 percent. Lactatetransformation to acetate was enhanced by low concentration of dissolvedoxygen during the logarithmic growth phase. Between 11 and 35oC, thegrowth rate obeyed the Arrhenius reaction rate-temperature relationship,with a maximum growth rate occurring at 35oC. S. oneidensis MR-1 was ableto grow over a wide range of pH (6-9). At neutral pH and temperaturesranging from 30-35oC, S. oneidensis MR-1 reduced 100 mu M Cr(VI) toCr(III) within 20 minutes in the exponential growth phase, and the growthrate was not affected by the addition of chromate; it reduced chromateeven faster at temperatures between 35 and 39oC. At low temperatures(<25oC), acidic (pH<6.5), or alkaline (pH>8.5) conditions, 100mu M Cr(VI) strongly inhibited growth and chromate reduction. Themini-bioreactor system enabled the rapid determination of theseparameters reproducibly and easily by performing very few experiments.Besides its use for examining parameters of interest to environmentalremediation, the device will also allow one to quickly assess parametersfor optimal production of recombinant proteins or secondarymetabolites

  12. Pyridine appended L-methionine: a novel chelating resin for pH dependent Cr speciation with scanning electron microscopic evidence and monitoring of yeast mediated green bio-reduction of Cr(VI) to Cr(III) in environmental samples.

    Science.gov (United States)

    Sahana, Animesh; Das, Sudipto; Banerjee, Arnab; Lohar, Sisir; Karak, Debasis; Das, Debasis

    2011-01-30

    Chemical speciation and pH dependent separation of Cr(III) and Cr(VI) species in environmental samples have been achieved by solid phase extraction using a new chelating resin containing pyridine appended L-methionine. Cr(III) is completely sorbed on the resin at pH 8.0 and Cr(VI) at pH 2.0. Hence a pH dependent separation of Cr(III) and Cr(VI) is possible with a limit of detection of 1.6 μg mL(-1) and 0.6 μg mL(-1) respectively. The sorption capacity of the resin for Cr(III) and Cr(VI) is 2.8 mmol g(-1) and 1.3 mmol g(-1) respectively. The sorption of chromium on the resin is supported by scanning electron microscopy (SEM). Complete desorption of Cr(III) and Cr(VI) from 1g of Cr loaded resin was achieved using 10 mL of 2 mol L(-1) HNO(3) and 6 mL of 3 mol L(-1) HNO(3) respectively. Quantitative recoveries of Cr(III) (pH 8.0) and Cr(VI) (pH 2.0) were found to be 96.0% and 98.0% respectively. Reduction efficiency of Rhodotornula mucilaginosa yeast from Cr(VI) to Cr(III) was monitored with this new resin. Concentrations of metal ions were measured by flame atomic absorption spectroscopy (FAAS). Copyright © 2010 Elsevier B.V. All rights reserved.

  13. Fast photoelectro-reduction of Cr{sup VI} over MoS{sub 2}@TiO{sub 2} nanotubes on Ti wire

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Lixia; Zheng, Xutong; Liu, Ming [High Level Laboratory of Jiangxi Province for Persistent Pollutants Control, Recycle and Reuse, Nanchang Hangkong University, Nanchang 330063 (China); Luo, Shenglian, E-mail: sllou@hnu.edu.cn [High Level Laboratory of Jiangxi Province for Persistent Pollutants Control, Recycle and Reuse, Nanchang Hangkong University, Nanchang 330063 (China); College of Material Science and Engineering, Nanchang Hangkong University, Nanchang 330063 (China); Luo, Yan [High Level Laboratory of Jiangxi Province for Persistent Pollutants Control, Recycle and Reuse, Nanchang Hangkong University, Nanchang 330063 (China); Li, Guifa [College of Material Science and Engineering, Nanchang Hangkong University, Nanchang 330063 (China)

    2017-05-05

    Highlights: • Few-layer MoS{sub 2} nanosheets decorated on the TiO{sub 2} NTAs via a facile hydrothermal method. • The composites possess a stable construction benefiting to the utilization of sunlight and electron transfer. • High concentration Cr{sup VI} can be fast reduced over MoS{sub 2}@TiO{sub 2} in the presence of appropriate LOAs and applied voltage. • Effect of LOAs, applied voltages and initial concentrations were performed. - Abstract: A stable MoS{sub 2} nanosheets@TiO{sub 2} NTAs composite was prepared via a simple hydrothermal process. Few-layer MoS{sub 2} nanosheets distributed on the TiO{sub 2} nanotube top surface and the inner walls rather than filling in the tubes, allowing abundant tubular channels open to environment and benefiting for efficient mass transport. Photocatalytic (PE) and photoelectrocatalytic (PEC) performance of the composite were evaluated on Cr{sup VI} reduction, with variable low molecule weight organic acids (LOAs) added as sacrificial electron donor to form a charge-transfer-complex (CTC) between LOAs and TiO{sub 2}/MoS{sub 2}, which is sensitive to the visible light illumination and could induce the photo-reduction of Cr{sup VI} and photo-oxidation of LOAs. The overall trend of Cr{sup VI} PEC rates are in the order as: L(+)-Tartaric acid > oxalic acid > citric acid > malic acid > amber acid, which is 103.9 > 62.5 > 31.2 > 21.6 > 2.5 mg/L min{sup −1} cm{sup −2}, respectively. The improved catalytic performance and excellent stability of the composite can be attributed to the abundant active adsorption and reaction sites on MoS{sub 2} nanosheets and the formation of a heterojunction between TiO{sub 2} and MoS{sub 2}. Moreover, the appropriate application of LOAs and voltage also have a great contribution to the utilization of sunlight and efficient separation of photogenerated carriers.

  14. Characterization and application of the hetero-junction ZnFe2O4/TiO2 for Cr(VI) reduction under visible light

    Science.gov (United States)

    Rekhila, G.; Trari, M.; Bessekhouad, Y.

    2017-06-01

    The spinel ZnFe2O4 prepared by nitrate route is used as dispersed photons collector capable to sensitize TiO2 under visible light and to reduce Cr(VI) into trivalent state. The transport properties, optical and photo-electrochemical characterizations are correlated, to build the energetic diagram of the hetero-system ZnFe2O4/TiO2/CrO4 - solution. A gap of 1.97 eV is obtained for the spinel from the diffuse reflectance. The conduction band of ZnFe2O4 (-1.47 V SCE) favors the electrons injection into TiO2, permitting a physical separation of the charge carriers. The oxidation of oxalic acid by photoholes prevents the corrosion of the spinel. The best configuration ZnFe2O4 (75 %)/TiO2 (25 %) is used to catalyze the downhill reaction (2HCrO4 - + 3C2H4O4 + 1.5O2 + 8H+ → 2Cr3+ + 6CO2 + 11 H2O, ∆ G° = -557 kcal mol-1). 60 % of Cr(VI) are reduced after 3 h of visible light illumination and the photoactivity follows a first-order kinetic with a half-life of 70 min. The water reduction competes with the HCrO4 - reduction which is the reason in the regression of the photoactivity; a hydrogen evolution rate of 24 µmol mg-1 h-1 is obtained.

  15. Preparation and characterization of Ag-doped TiO{sub 2} nanomaterials and their photocatalytic reduction of Cr(VI) under visible light

    Energy Technology Data Exchange (ETDEWEB)

    Lei, X.F., E-mail: leixuefei69@163.com [School of Resources and Materials, Northeastern University at Qinhuangdao, Qinhuangdao 066004 (China); Institute of Metallurgical Resource and Environmental Engineering, Northeastern University, Shenyang 110819 (China); Liaoning Key Laboratory of Metallurgical Resource Recycling Science, Shenyang 110819 (China); Liaoning Engineering and Technology Research Center of Boron Resource, Comprehensive Utilization, Shenyang 110819 (China); Liaoning Provincial Universities Key Laboratory of Boron Resource Ecological, Utilization Technology and Boron Materials, Shenyang 110819 (China); Xue, X.X.; Yang, H. [Institute of Metallurgical Resource and Environmental Engineering, Northeastern University, Shenyang 110819 (China); Liaoning Key Laboratory of Metallurgical Resource Recycling Science, Shenyang 110819 (China); Liaoning Engineering and Technology Research Center of Boron Resource, Comprehensive Utilization, Shenyang 110819 (China); Liaoning Provincial Universities Key Laboratory of Boron Resource Ecological, Utilization Technology and Boron Materials, Shenyang 110819 (China)

    2014-12-01

    Graphical abstract: - Highlights: • Ag-doping in TiO{sub 2} can preserve the anatase form to higher temperature. • Ag-doped TiO{sub 2} samples can absorb both UV and visible light. • The band gap energy of the sample significantly reduced after Ag-doping. • Ag-doped TiO{sub 2} samples effective for visible light-induced reduction of Cr(VI). - Abstract: Ag-doped TiO{sub 2} nanomaterials (Ag–TiO{sub 2}) were prepared by a sol–gel method. The structures of Ag–TiO{sub 2} nanomaterials were characterized by X-ray diffraction (XRD), UV–vis diffuse reflectance spectra (DRS), X-ray photoluminescence (PL) spectroscopy, X-ray photoelectron spectroscopy (XPS), thermogravimetry and differential thermal analysis (TG-DTA), Fourier transform infrared spectroscopy (FT-IR), transmission electron microscope (TEM), scanning electron microscopy (SEM) and nitrogen adsorption–desorption isotherms. The photocatalytic activities were checked through the photocatalytic reduction of Cr(VI) as a model compound under visible light irradiation. The results showed that the Ag doping and the calcination temperature played an important role on the microstructure and photocatalytic activity of the samples. Ag-doped TiO{sub 2} samples calcinated at 400 °C exhibits higher photocatalytic activity than that of the other samples under visible light irradiation.

  16. Fabrication of bimodal-pore SrTiO3 microspheres with excellent photocatalytic performance for Cr(VI) reduction under simulated sunlight.

    Science.gov (United States)

    Yang, Dong; Sun, Yuanyuan; Tong, Zhenwei; Nan, Yanhu; Jiang, Zhongyi

    2016-07-15

    Solving the increasing contamination from toxic heavy metal ions in wastewater is an imperative issue in photocatalysis research area. In this study, three-dimensional (3D) porous SrTiO3 microspheres have been fabricated by a sol-gel-templating method using the agarose gel bead containing SrCO3 granules as the template. The resultant SrTiO3 microspheres, several tens of micrometers in diameter, exhibit a bimodal pore structure, in which the macropore about 70-150nm in size stems from SrCO3 granules and the mesopore about 3nm is formed via removing the agarose fiber embedded in the composite microspheres. The porous framework of SrTiO3 microspheres is assembled by regular single-crystalline SrTiO3 nanocubes with an edge length of 100±10nm. The highly interconnected porous network renders numerous pathways for the rapid mass transport, strong adsorption of reactants and multi-reflection of incident light. Moreover, the as-prepared SrTiO3 microspheres exhibit excellent photocatalytic performance for the Cr(VI) reduction under simulated sunlight, which can reduce nearly 100% Cr(VI) at pH 2 within 2h and retain a relatively high reduction ability after six recycles. Copyright © 2016 Elsevier B.V. All rights reserved.

  17. Metal organic framework g-C3N4/MIL-53(Fe) heterojunctions with enhanced photocatalytic activity for Cr(VI) reduction under visible light

    Science.gov (United States)

    Huang, Wenyuan; Liu, Ning; Zhang, Xiaodong; Wu, Minghong; Tang, Liang

    2017-12-01

    In this study, hybrid nanocomposites based on Fe-based MOF and graphitic carbon nitride (g-C3N4) were developed by a facile solvothermal method. The as-prepared materials were characterized by XRD, FESEM, TEM, XPS and PL analysis. It was showed that the introduction of a certain amount of g-C3N4 on the surface of MIL-53(Fe) would improve the separation and migration rate of photo-induced charges, consequently resulting in the boost of photocatalytic efficiency. Compared with g-C3N4 and MIL-53(Fe), the CMFe composites displayed more excellent visible light-resposive photocatalytic activity for the reduction of Cr(VI). The optimal doping content of g-C3N4 in g-C3N4/MIL-53(Fe) composite was determined to be 3.0 wt%, and it showed about 2.1 and 2.0 times as high photocatalytic efficiency for the reduction of Cr(VI) as that of pure g-C3N4 and MIL-53(Fe), respectively. Meanwhile, the composite exhibited good reusability and stability in the process of cyclic experiments. A possible photocatalytic reaction mechanism was also investigated in detail by the related electrochemical analysis.

  18. Visible light-responded C, N and S co-doped anatase TiO{sub 2} for photocatalytic reduction of Cr(VI)

    Energy Technology Data Exchange (ETDEWEB)

    Lei, X.F., E-mail: leixuefei69@163.com [School of Resources and Materials, Northeastern University at Qinhuangdao, Qinhuangdao 066004 (China); Institute of Metallurgical Resource and Environmental Engineering, Northeastern University, Shenyang 110819 (China); Liaoning Key Laboratory of Metallurgical Resource Recycling Science, Shenyang 110819 (China); Liaoning Engineering and Technology Research Center of Boron Resource, Comprehensive, Utilization, Shenyang 110819 (China); Liaoning Provincial Universities Key Laboratory of Boron Resource Ecological, Utilization, Technology and Boron Materials, Shenyang 110819 (China); Xue, X.X.; Yang, H. [Institute of Metallurgical Resource and Environmental Engineering, Northeastern University, Shenyang 110819 (China); Liaoning Key Laboratory of Metallurgical Resource Recycling Science, Shenyang 110819 (China); Liaoning Engineering and Technology Research Center of Boron Resource, Comprehensive, Utilization, Shenyang 110819 (China); Liaoning Provincial Universities Key Laboratory of Boron Resource Ecological, Utilization, Technology and Boron Materials, Shenyang 110819 (China); Chen, C.; Li, X.; Pei, J.X.; Niu, M.C.; Yang, Y.T.; Gao, X.Y. [School of Resources and Materials, Northeastern University at Qinhuangdao, Qinhuangdao 066004 (China)

    2015-10-15

    The (C, N and S) co-doped TiO{sub 2} (TH-TiO{sub 2}) samples were synthesized by a sol-gel method calcined at 500 °C, employing butyl titanate as the titanium source and thiourea as the dopant. The structures of TH-TiO{sub 2} samples were characterized by X-ray diffraction (XRD), Transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS), UV–vis diffuse reflectance spectra (DRS), photoluminescence (PL) spectroscopy, Thermo gravimetry and differential thermal analysis (TG-DTA), Scanning electron microscopy (SEM) and nitrogen adsorption–desorption isotherms. The photocatalytic activities were checked through the photocatalytic reduction of Cr(VI) as a model compound under visible light irradiation. The results showed that the thiourea content played an important role on the microstructure and photocatalytic activity of the samples. According to XPS results, (C, N and S) atoms were successfully co-doped into the nanostructures of TH-TiO{sub 2} samples. TH-TiO{sub 2} samples with thiourea: Ti molar ratio of 1.5 exhibits higher photocatalytic activity than that of the other samples under visible light irradiation, which can be attributed to the synergic effect of the pure anatase structure, the higher light absorption characteristics in visible regions, separation efficiency of electron–hole pairs, the specific surface area and the optimum (C, N and S) content. - Graphical abstract: (C, N and S) co-doped TiO{sub 2} samples show good photocatalytic activity for Cr (VI) reduction under visible light irradiation. - Highlights: • (C, N and S) co-doping in TH-TiO{sub 2} samples can promote the formation of the pure anatase structure. • (C, N and S) atoms were successfully co-doped into the nanostructures of TH-TiO{sub 2} samples. • The band gap energy of TH-TiO{sub 2} samples reduced after (C, N and S) co-doping. • (C, N and S) co-doped TiO{sub 2} samples were effective for the photocatalytic reduction of Cr(VI) under visible light

  19. Highly enhanced photocatalytic reduction of Cr(VI) on AgI/TiO{sub 2} under visible light irradiation: Influence of calcination temperature

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Qi; Shi, Xiaodong; Xu, Jianjia [School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310018 (China); Crittenden, John C. [The Brook Byer Institute for Sustainable Systems and School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta,GA 30332 (United States); Liu, Enqin; Zhang, Yi [School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310018 (China); Cong, Yanqing, E-mail: yqcong@hotmail.com [School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310018 (China)

    2016-04-15

    Highlights: • β-AgI riched AgI/TiO2 was obtained after simple heat pretreatment at 350 °C. • Greatly enhanced visible light response was observed on AgI/TiO2-350. • AgI/TiO2-350 exhibited superior photocatalytic activity and stability. • 5 times rate constant for Cr(VI) reduction was achieved. • More efficient separation and easier transfer of e{sup −}–h{sup +} pairs were facilitated. - Abstract: AgI/TiO{sub 2} was prepared using a dissolution-precipitation method, followed by calcination at different temperatures (100–700 °C). The as-prepared AgI/TiO{sub 2} powders were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible diffuse reflectance spectroscopy (UV–Vis-DRS) and electrochemical impedance spectroscopy (EIS). The results revealed that calcination temperature significantly impacted the visible light absorption of AgI/TiO{sub 2} along with a shift from metastable γ-AgI to relatively stable β-AgI. We found that highest photocatalytic reduction rate of Cr(VI) and β-AgI content were obtained for a calcination temperature of 350 °C. Furthermore, the pseudo-first order rate constant was five times that for a photocatalyst calcined at 100 °C. The dramatically enhanced reduction rate of Cr(VI) was attributed to enhanced visible light absorption and greatly reduced charge transfer resistance, which eventually facilitates more efficient separation and easier transfer of photogenerated electron–hole pairs to the catalyst surface. Other experimental conditions were also carefully investigated and optimized with initial AgI loading percentage (5%), catalyst dosage (1.0 g/L), coexisting organics (1.0 mmol/L EDTA) and pH (1–2). The optimal AgI/TiO{sub 2} exhibited good stability with little change in activity after 5 cycles.

  20. Hollow spheric Ag–Ag{sub 2}S/TiO{sub 2} composite and its application for photocatalytic reduction of Cr(VI)

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Dandan; Xu, Gangqiang; Chen, Feng, E-mail: fengchen@ecust.edu.cn

    2015-10-01

    Graphical abstract: - Highlights: • Hollow spheric Ag–Ag{sub 2}S/TiO{sub 2} composites were prepared. • Ag–Ag{sub 2}S/TiO{sub 2} composite shows prior UV and visible photocatalytic activities. • Schottky barrier between Ag and Ag{sub 2}S (TiO{sub 2}) promotes the photocatalytic activity. • Low bandgap of Ag{sub 2}S gives Ag–Ag{sub 2}S/TiO{sub 2} a good visible photocatalytic activity. • The photocatalytic activity of Ag–Ag{sub 2}S/TiO{sub 2} is maintained well after recycled. - Abstract: Hollow spheric Ag–Ag{sub 2}S was prepared by in-situ chemical transforming of sacrificial Cu{sub 2}S templates with AgNO{sub 3} solution. Hollow spheric Ag–Ag{sub 2}S/TiO{sub 2} composites were then prepared by assembling TiO{sub 2} grains around the Ag–Ag{sub 2}S spheres with hydrothermal treatment of Ag–Ag{sub 2}S with Ti precursor at 180 °C. X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), Inductively coupled plasma-atomic emission spectroscopy (ICP-AES) were adopted to characterize the as-prepared composite. Ag–Ag{sub 2}S/TiO{sub 2} composite has obvious absorption at both UV and visible regions, and shows prior photocatalytic activity for the reduction of Cr(VI) under both UV and visible irradiation. Particularly, the Ag–Ag{sub 2}S/TiO{sub 2}-5 and Ag–Ag{sub 2}S/TiO{sub 2}-10 show the highest activity for the photocatalytic reduction of Cr(VI) under UV and visible irradiation, respectively. The Schottky barrier between Ag and Ag{sub 2}S (and TiO{sub 2} as well) and the heterojunction between the Ag{sub 2}S and TiO{sub 2} are suggested as the main reasons that enhance the photocatalytic reduction of Cr(VI). The photocatalytic activity of Ag–Ag{sub 2}S/TiO{sub 2} composite is maintained well after being recycled several times.

  1. New approach in modeling Cr(VI) sorption onto biomass from metal binary mixtures solutions

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Chang [College of Environmental Science and Engineering, Anhui Normal University, South Jiuhua Road, 189, 241002 Wuhu (China); Chemical Engineering Department, Escola Politècnica Superior, Universitat de Girona, Ma Aurèlia Capmany, 61, 17071 Girona (Spain); Fiol, Núria [Chemical Engineering Department, Escola Politècnica Superior, Universitat de Girona, Ma Aurèlia Capmany, 61, 17071 Girona (Spain); Villaescusa, Isabel, E-mail: Isabel.Villaescusa@udg.edu [Chemical Engineering Department, Escola Politècnica Superior, Universitat de Girona, Ma Aurèlia Capmany, 61, 17071 Girona (Spain); Poch, Jordi [Applied Mathematics Department, Escola Politècnica Superior, Universitat de Girona, Ma Aurèlia Capmany, 61, 17071 Girona (Spain)

    2016-01-15

    In the last decades Cr(VI) sorption equilibrium and kinetic studies have been carried out using several types of biomasses. However there are few researchers that consider all the simultaneous processes that take place during Cr(VI) sorption (i.e., sorption/reduction of Cr(VI) and simultaneous formation and binding of reduced Cr(III)) when formulating a model that describes the overall sorption process. On the other hand Cr(VI) scarcely exists alone in wastewaters, it is usually found in mixtures with divalent metals. Therefore, the simultaneous removal of Cr(VI) and divalent metals in binary mixtures and the interactive mechanism governing Cr(VI) elimination have gained more and more attention. In the present work, kinetics of Cr(VI) sorption onto exhausted coffee from Cr(VI)–Cu(II) binary mixtures has been studied in a stirred batch reactor. A model including Cr(VI) sorption and reduction, Cr(III) sorption and the effect of the presence of Cu(II) in these processes has been developed and validated. This study constitutes an important advance in modeling Cr(VI) sorption kinetics especially when chromium sorption is in part based on the sorbent capacity of reducing hexavalent chromium and a metal cation is present in the binary mixture. - Highlights: • A kinetic model including Cr(VI) reduction, Cr(VI) and Cr(III) sorption/desorption • Synergistic effect of Cu(II) on Cr(VI) elimination included in the model • Model validation by checking it against independent sets of data.

  2. Advanced oxidation process based on the Cr(III)/Cr(VI) redox cycle.

    Science.gov (United States)

    Bokare, Alok D; Choi, Wonyong

    2011-11-01

    Oxidative degradation of aqueous organic pollutants, using 4-chlorophenol (4-CP) as a main model substrate, was achieved with the concurrent H(2)O(2)-mediated transformation of Cr(III) to Cr(VI). The Fenton-like oxidation of 4-CP is initiated by the reaction between the aquo-complex of Cr(III) and H(2)O(2), which generates HO(•) along with the stepwise oxidation of Cr(III) to Cr(VI). The Cr(III)/H(2)O(2) system is inactive in acidic condition, but exhibits maximum oxidative capacity at neutral and near-alkaline pH. Since we previously reported that Cr(VI) can also activate H(2)O(2) to efficiently generate HO(•), the dual role of H(2)O(2) as an oxidant of Cr(III) and a reductant of Cr(VI) can be utilized to establish a redox cycle of Cr(III)-Cr(VI)-Cr(III). As a result, HO(•) can be generated using both Cr(III)/H(2)O(2) and Cr(VI)/H(2)O(2) reactions, either concurrently or sequentially. The formation of HO(•) was confirmed by monitoring the production of p-hydroxybenzoic acid from [benzoic acid + HO(•)] as a probe reaction and by quenching the degradation of 4-CP in the presence of methanol as a HO(•) scavenger. The oxidation rate of 4-CP in the Cr(III)/H(2)O(2) solution was highly influenced by pH, which is ascribed to the hydrolysis of Cr(III)(H(2)O)(n) into Cr(III)(H(2)O)(n-m)(OH)(m) and the subsequent condensation to oligomers. The present study proposes that the Cr(III)/H(2)O(2) combined with Cr(VI)/H(2)O(2) process is a viable advanced oxidation process that operates over a wide pH range using the reusable redox cycle of Cr(III) and Cr(VI).

  3. Facile preparation of magnetic mesoporous MnFe2O4@SiO2-CTAB composites for Cr(VI) adsorption and reduction.

    Science.gov (United States)

    Li, Na; Fu, Fenglian; Lu, Jianwei; Ding, Zecong; Tang, Bing; Pang, Jiabin

    2017-01-01

    Chromium-contaminated water is regarded as one of the biggest threats to human health. In this study, a novel magnetic mesoporous MnFe2O4@SiO2-CTAB composite was prepared by a facile one-step modification method and applied to remove Cr(VI). X-ray diffraction, scanning electron microscopy, transmission electron microscopy, specific surface area, and vibrating sample magnetometer were used to characterize MnFe2O4@SiO2-CTAB composites. The morphology analysis showed that the composites displayed a core-shell structure. The outer shell was mesoporous silica with CTAB and the core was MnFe2O4 nanoparticles, which ensured the easy separation by an external magnetic field. The performance of MnFe2O4@SiO2-CTAB composites in Cr(VI) removal was far better than that of bare MnFe2O4 nanoparticles. There were two reasons for the effective removal of Cr(VI) by MnFe2O4@SiO2-CTAB composites: (1) mesoporous silica shell with abundant CTA(+) significantly enhanced the Cr(VI) adsorption capacity of the composites; (2) a portion of Cr(VI) was reduced to less toxic Cr(III) by MnFe2O4, followed by Cr(III) immobilized on MnFe2O4@SiO2-CTAB composites, which had been demonstrated by X-ray photoelectron spectroscopy results. The adsorption of Cr(VI) onto MnFe2O4@SiO2-CTAB followed the Freundlich isotherm model and pseudo-second-order model. Tests on the regeneration and reuse of the composites were performed. The removal efficiency of Cr(VI) still retained 92.4% in the sixth cycle. MnFe2O4@SiO2-CTAB composites exhibited a great potential for the removal of Cr(VI) from water. Copyright © 2016 Elsevier Ltd. All rights reserved.

  4. Photocatalytic reduction of Cr(VI) on the new hetero-system CuAl{sub 2}O{sub 4}/TiO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Gherbi, R. [Laboratory of Reaction Engineering, Faculty of Mechanic and Engineering Processes, USTHB, BP 32, 16111 Algiers (Algeria); Nasrallah, N. [Laboratory of Reaction Engineering, Faculty of Mechanic and Engineering Processes, USTHB, BP 32, 16111 Algiers (Algeria); Equipe chimie et Ingenierie des procedes, UMR CNRS 6226, E.N.S.C.R., Avenue du General Leclerc, CS 50837, 35708 Rennes Cedex 7 (France); Amrane, A. [Equipe chimie et Ingenierie des procedes, UMR CNRS 6226, E.N.S.C.R., Avenue du General Leclerc, CS 50837, 35708 Rennes Cedex 7 (France); Maachi, R. [Laboratory of Reaction Engineering, Faculty of Mechanic and Engineering Processes, USTHB, BP 32, 16111 Algiers (Algeria); Trari, M., E-mail: solarchemistry@gmail.com [Laboratory of Storage and Valorization of Renewable Energies, Faculty of Chemistry, USTHB, BP 32, 16111 Algiers (Algeria)

    2011-02-28

    Visible light driven HCrO{sub 4}{sup -} reduction was successfully achieved over the new hetero-system CuAl{sub 2}O{sub 4}/TiO{sub 2}. The spinel, elaborated by nitrate route, was characterized photo electrochemically. The optical gap was found to be 1.70 eV and the transition is directly allowed. The conduction band (-1.05 V{sub SCE}) is located below that of TiO{sub 2}, more negative than the HCrO{sub 4}{sup -}/Cr{sup 3+} level (+0.58 V{sub SCE}) yielding a thermodynamically feasible chromate reduction upon visible illumination. CuAl{sub 2}O{sub 4} is stable against photo corrosion by holes consumption reaction involving salicylic acid which favors the charges separation. There is a direct correlation between the dark adsorption and the photo activity. A reduction of more than 95% of chromate was achieved after 3 h irradiation at pH 2 with an optimal mass ratio (CuAl{sub 2}O{sub 4}/TiO{sub 2}) equal to 1/3. The reduction follows a first order kinetic with a half life of {approx}1 h and a quantum yield of 0.11% under polychromatic light. Prolonged illumination was accompanied by a deceleration of the Cr(VI) reduction thanks to the competitive water discharge. The hydrogen evolution, an issue of energetic concern, took place with a rate of 3.75 cm{sup 3} (g catalyst){sup -1} h{sup -1}.

  5. Fabrication uniform hollow Bi2S3 nanospheres via Kirkendall effect for photocatalytic reduction of Cr(VI) in electroplating industry wastewater.

    Science.gov (United States)

    Luo, Sheng; Qin, Fan; Ming, Yin'an; Zhao, Huiping; Liu, Yunling; Chen, Rong

    2017-10-15

    Hazardous hexavalent chromium removal from wastewater is an urgent issue in industry environmental pollution. In this work, hollow Bi2S3 nanospheres have been successfully synthesized from unique Bi2O3 porous nanospheres via Kirkendall effect through hydrothermal process. It was found that the sulfur source and the initial Bi2O3 templates played key roles in the formation of the uniform morphologies and structures through an anion exchange process. Compared with other Bi2S3 samples, the synthesized hollow Bi2S3 nanospheres exhibited much enhanced photocatalytic ability for Cr(VI) photoreduction. XPS analysis demonstrated that Cr(VI) was reduced to less harmful Cr(III) species over hollow Bi2S3 nanospheres under visible-light irradiation. More importantly, the hollow Bi2S3 nanospheres remained high efficiency and good stability in the recycling Cr(VI) photoreduction, and exhibited remarkable Cr(VI) removal ability in actual electroplating industry wastewater treatment. Copyright © 2017 Elsevier B.V. All rights reserved.

  6. Microstructural analyses of Cr(VI) speciation in chromite ore processing Residue (COPR)

    Energy Technology Data Exchange (ETDEWEB)

    CHRYSOCHOOU, MARIA; FAKRA, SIRINE C .; Marcus, Matthew A.; Moon, Deok Hyun; Dermatas, Dimitris

    2010-03-01

    The speciation and distribution of Cr(VI) in the solid phase was investigated for two types of chromite ore processing residue (COPR) found at two deposition sites in the United States: gray-black (GB) granular and hard brown (HB) cemented COPR. COPR chemistry and mineralogy were investigated using micro-X-ray absorption spectroscopy and micro-X-ray diffraction, complemented by laboratory analyses. GB COPR contained 30percent of its total Cr(VI) (6000 mg/kg) as large crystals(>20 ?m diameter) of a previously unreported Na-rich analog of calcium aluminum chromate hydrates. These Cr(VI)-rich phases are thought to be vulnerable to reductive and pH treatments. More than 50percent of the Cr(VI) was located within nodules, not easily accessible to dissolved reductants, and bound to Fe-rich hydrogarnet, hydrotalcite, and possibly brucite. These phases are stable over a large pH range, thus harder to dissolve. Brownmilleritewasalso likely associated with physical entrapment of Cr(VI) in the interior of nodules. HB COPR contained no Cr(VI)-rich phases; all Cr(VI) was diffuse within the nodules and absent from the cementing matrix, with hydrogarnet and hydrotalcite being the main Cr(VI) binding phases. Treatment ofHBCOPRis challenging in terms of dissolving the acidity-resistant, inaccessible Cr(VI) compounds; the same applies to ~;;50percent of Cr(VI) in GB COPR.

  7. One stone two birds: novel carbon nanotube/Bi4VO8Cl photocatalyst for simultaneous organic pollutants degradation and Cr(VI) reduction.

    Science.gov (United States)

    Zhang, Xia; Shi, Dongyang; Fan, Jing

    2017-08-24

    In this work, visible light-responsive carbon nanotubes (CNTs)/Bi4VO8Cl composite photocatalysts have been prepared by a facile in situ hydrothermal method and characterized by various techniques. The photocatalytic properties of the photocatalysts are evaluated by the degradation of refractory azo-dye methyl orange (MO), hexavalent chromium Cr(VI), and bisphenol A (BPA) in water under visible light irradiation. It is found that the as-prepared composite with 4 wt% CNTs shows an optimal photocatalytic performance, and its photocatalytic activity is 30% higher than that of pure Bi4VO8Cl. The enhanced photocatalytic activity is ascribed to the synergetic effects induced by increased light absorption, increased adsorption efficiency for pollutant, and suppressed recombination rate of photogenerated charge carriers. Furthermore, efficient removals of Cr(VI), bisphenol A (BPA), and combined contamination of Cr(VI) and BPA over CNTs/Bi4VO8Cl composite further confirm that the degradation of organic pollutants is a photocatalytic mechanism rather than photosensitization of dye. Of particular importance is that removal efficiency of single pollutant can be promoted by the coexistence of the Cr(VI) and organics. The mechanism of synergetic promotion is discussed and attributed to the accelerated separation of charge carriers resulted from their simultaneously being captured by pollutants. Moreover, the CNTs/Bi4VO8Cl composite exhibits good stability and recycling performance in the photocatalytic degradation process. Therefore, the composite photocatalysts developed in the present work are expected to have the potential in purification of complex wastewater. Graphical abstract The separation of photogenerated charge carriers and adsorbing capacity as well as visible light absorption ability of Bi4VO8Cl are significantly promoted by coupling with carbon nanotubes. Simultaneous removal of Cr(VI) and organic pollutants can be achieved by CNTs/Bi4VO8Cl composite photocatalysts

  8. Bioreduction of Cr (VI) by potent novel chromate resistant alkaliphilic ...

    African Journals Online (AJOL)

    Isolation of Cr (VI) resistant alkaliphilic bacteria from sediment and water samples collected from Wadi Natrun hypersaline Soda lakes (located in northern Egypt), resulted in isolation of several alkaliphilic bacterial strains that can tolerate up to 2.94 g/l of Cr (VI) in alkaline medium. However, with increasing Cr (VI) ...

  9. Removal of Cr(VI) and humic acid by using TiO2 photocatalysis.

    Science.gov (United States)

    Yang, Jae-Kyu; Lee, Seung-Mok

    2006-06-01

    The removal efficiencies of Cr(VI) and HA, using a TiO(2)-mediated photocatalytic process, were investigated with variations in the pH, TiO(2) dosage and Cr(VI)/HA ratio. During the photocatalytic reaction, the total removal of Cr(VI) occurred through adsorption onto TiO(2), as well as its reduction to Cr(III). However, oxidation and adsorption were identified as important removal processes for the treatment of HA. Due to the anionic type adsorption onto TiO(2) and its acid-catalyzed photocatalytic reduction, the removal of Cr(VI) decreased with increasing pH, while that of HA increased with increasing pH. The TiO(2) dosage was also an important parameter for the removal of Cr(VI). As the TiO(2) dosage was increased to 2.5 g l(-1), the removal of Cr(VI) was continuously enhanced, but decreased at dosages above 3 g l(-1) due to the increased blockage of the incident UV light used for the photocatalytic reaction. The removal of Cr(VI) was greatly enhanced when the system contained both HA and Cr(VI) compared to Cr(VI) alone. Also, the removal of HA was greatly enhanced when the system contained both HA and Cr(VI) compared to HA alone. The removal of Cr(VI) was continuously enhanced as the HA concentration gradually increased; however, no further increase was observed above 20 mg l(-1) HA due to the increased absorption of the UV light. This result supports that the photocatalytic reaction, with illuminated TiO(2), could be applied to more effectively treat wastewater containing both Cr(VI) and HA than that containing a single species only.

  10. Kinetics and Products of Chromium(VI) Reduction by Iron(II/III)-Bearing Clay Minerals.

    Science.gov (United States)

    Joe-Wong, Claresta; Brown, Gordon E; Maher, Kate

    2017-09-05

    Hexavalent chromium is a water-soluble pollutant, the mobility of which can be controlled by reduction of Cr(VI) to less soluble, environmentally benign Cr(III). Iron(II/III)-bearing clay minerals are widespread potential reductants of Cr(VI), but the kinetics and pathways of Cr(VI) reduction by such clay minerals are poorly understood. We reacted aqueous Cr(VI) with two abiotically reduced clay minerals: an Fe-poor montmorillonite and an Fe-rich nontronite. The effects of ionic strength, pH, total Fe content, and the fraction of reduced structural Fe(II) [Fe(II)/Fe(total)] were examined. The last variable had the largest effect on Cr(VI) reduction kinetics: for both clay minerals, the rate constant of Cr(VI) reduction varies by more than 3 orders of magnitude with Fe(II)/Fe(total) and is described by a linear free energy relationship. Under all conditions examined, Cr and Fe K-edge X-ray absorption near-edge structure spectra show that the main Cr-bearing product is a Cr(III)-hydroxide and that Fe remains in the clay structure after reacting with Cr(VI). This study helps to quantify our understanding of the kinetics of Cr(VI) reduction by Fe(II/III)-bearing clay minerals and may improve predictions of Cr(VI) behavior in subsurface environments.

  11. Integrated Ecogenomics Study for Bioremediation of Cr(VI) at Hanford 100H Area

    Energy Technology Data Exchange (ETDEWEB)

    Chakraborty, Romy; Chakraborty, Romy

    2008-08-12

    Hexavalent chromium is a widespread contaminant found in groundwater. In order to stimulate microbially mediated Cr(VI)-reduction, a poly-lactate compound was injected into Cr(VI)-contaminated aquifers at site 100H at Hanford. Investigation of bacterial community composition using high-density DNA microarray analysis of 16S rRNA gene products revealed a stimulation of Pseudomonas, Desulfovibrio and Geobacter species amongst others. Enrichment of these organisms coincided with continued Cr(VI) depletion. Functional gene-array analysis of DNA from monitoring well indicated high abundance of genes involved in nitrate-reduction, sulfate-reduction, iron-reduction, methanogenesis, chromium tolerance/reduction. Clone-library data revealed Psedomonas was the dominant genus in these samples. Based on above results, we conducted lab investigations to study the dominant anaerobic culturable microbial populations present at this site and their role in Cr(VI)-reduction. Enrichments using defined anaerobic media resulted in isolation of an iron-reducing, a sulfate-reducing and a nitrate-reducing isolate among several others. Preliminary 16S rDNA sequence analysis identified the isolates as Geobacter metallireducens, Pseudomonas stutzeri and Desulfovibrio vulgaris species respectively. The Pseudomonas isolate utilized acetate, lactate, glycerol and pyruvate as alternative carbon sources, and reduced Cr(VI). Anaerobic washed cell suspension of strain HLN reduced almost 95?M Cr(VI) within 4 hr. Further, with 100?M Cr(VI) as sole electron-acceptor, cells grew to 4.05 x 107 /ml over 24 h after an initial lag, demonstrating direct enzymatic Cr(VI) reduction coupled to growth. These results demonstrate that Cr(VI)-immobilization at Hanford 100H site could be mediated by direct microbial metabolism in addition to indirect chemical reduction of Cr(VI) by end-products of microbial activity.

  12. Removal of Cr(VI) from groundwater by Fe(0)

    Science.gov (United States)

    Gao, Yanjiao; Liu, Rui

    2017-11-01

    This research was conducted to investigate the treatment of hexavalent chromium (Cr(VI)) by iron powder (Fe(0)) columns of simulated permeable reactive barriers with and without calcium carbonate (CaCO3). Two columns filled with Fe(0) were used as Cr(VI) removal equipment running at a flow velocity of 10 ml/min at room temperature. After 200 days running of the two columns, the results showed that Fe(0) was an effective material for Cr(VI) reduction with an average removal rate of above 84.6%. The performance of Column 2 with CaCO3 was better than Column 1 without CaCO3 in terms of average Cr(VI) removal rate. The presence of CaCO3 buffered the increasing pH caused by Fe(0) corrosion in Column 2 and enhanced the removal rate of Column 2. Scanning Electron Microscopy (SEM) images of Fe(0) in the three stages of running of the two columns illustrated that the coat layer of Column 1 was a little thicker than that of Column 2. Energy-dispersive spectrometry (EDS) results showed that the surface of Fe(0) of Column 2 contained more chromium elements. Raman spectroscopy found that all iron oxide was generated on the Fe(0) surface of Column 1 and Column 2 and chromium class objects were only detected on Fe(0) surface in Column 2.

  13. Heterotrophic and elemental-sulfur-based autotrophic denitrification processes for simultaneous nitrate and Cr(VI) reduction.

    Science.gov (United States)

    Sahinkaya, Erkan; Kilic, Adem

    2014-03-01

    Nitrate and chromate can be present together in water resources as nitrate is a common co-contaminant in surface and ground waters. This study aims at comparatively evaluating simultaneous chromate and nitrate reduction in heterotrophic and sulfur-based autotrophic denitrifying column bioreactors. In sulfur-based autotrophic denitrification process, elemental sulfur and nitrate act as an electron donor and an acceptor, respectively, without requirement of organic supplementation. Autotrophic denitrification was complete and not adversely affected by chromate up to 0.5 mg/L. Effluent chromate concentration was reduction was attained up to 10 mg/L. Although autotrophic denitrification rate was much lower compared with heterotrophic one, it may be preferred in drinking water treatment due to the elimination of organic supplementation and the risk of treated effluent contamination. Copyright © 2013 Elsevier Ltd. All rights reserved.

  14. Performance of NiFe2O4-SiO2-TiO2 Magnetic Photocatalyst for the Effective Photocatalytic Reduction of Cr(VI in Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Mike O. Ojemaye

    2017-01-01

    Full Text Available Investigation into the reduction of Cr(VI in aqueous solution was carried out through some batch photocatalytic studies. The photocatalysts used were silica coated nickel ferrite nanoparticles (NiFe2O4-SiO2, nickel ferrite titanium dioxide (NiFe2O4-TiO2, nickel ferrite silica titanium dioxide (NiFe2O4-SiO2-TiO2, and titanium dioxide (TiO2. The characterization of the materials prepared via stepwise synthesis using coprecipitation and sol-gel methods were carried out with the aid of X-ray diffraction (XRD, transmission electron microscopy (TEM, scanning electron microscopy (SEM, Fourier transform infrared (FTIR spectroscopy, thermal gravimetric analysis (TGA, and vibrating sample magnetometry (VSM. The reduction efficiency was studied as a function of pH, photocatalyst dose, and contact time. The effects of silica interlayer between the magnetic photocatalyst materials reveal that reduction efficiency of NiFe2O4-SiO2-TiO2 towards Cr(VI was higher than that of NiFe2O4-TiO2. However, TiO2 was observed to have the highest reduction efficiency at all batch photocatalytic experiments. Kinetics study shows that photocatalytic reduction of Cr(VI obeyed Langmuir-Hinshelwood model and first-order rate kinetics. Regenerability study also suggested that the photocatalyst materials can be reused.

  15. Enhancement strategies for Cu(II), Cr(III) and Cr(VI) remediation by a variety of seaweed species.

    Science.gov (United States)

    Murphy, V; Hughes, H; McLoughlin, P

    2009-07-15

    Various chemical treatments have been applied to six brown, red and green seaweed species with a view to enhancing their metal removal for Cu(II), Cr(III) and Cr(VI). Treatment with acetone resulted in the greatest enhancement for both cationic and anionic species with relatively low mass losses (15-35%), indicating its low risk to biomass operational stability. Cation binding was increased by 69%, while the total Cr removal was augmented by 15%. Cr(VI) binding was shown to be an adsorption-coupled reduction, whereby Cr(VI) was bound to the biomass surface at pH 2 and subsequently reduced to Cr(III). Acetone treatment also resulted in biomasses that were capable of converting up to 83% of Cr(VI) in solution to Cr(III). Blocking of carboxyl and amino functionalities had significant negative effects both on total Cr removal as well as percentage conversion of Cr(VI) to Cr(III). Results therefore indicated the significant role played by these moieties in metal binding to these seaweeds. Potentiometric titrations displayed agreement between the degree of esterification and the decrease in Cu(II) removal for Ulva spp. and Polysiphonia lanosa. FTIR analysis identified changes in biomass functionality and availability after chemical modification, the results of which were in agreement with metal removal studies. In conclusion, these biosorbents represent suitable candidates to replace conventional removal technologies for metal bearing wastewaters, in particular for the detoxification of hazardous Cr(VI) waste streams.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-09-15

    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)

  17. Bioaccumulation and subcellular partitioning of Cr(III) and Cr(VI) in the freshwater green alga Chlamydomonas reinhardtii

    Energy Technology Data Exchange (ETDEWEB)

    Aharchaou, Imad [Laboratoire Interdisciplinaire des Environnements Continentaux, UMR 7360, Université de Lorraine and CNRS, 8 rue du Général Delestraint, 57070 Metz (France); Rosabal, Maikel; Liu, Fengjie [Institut National de la Recherche Scientifique, Centre Eau Terre Environnement (INRS-ETE), 490 rue de la Couronne, Québec (Québec) G1K 9A9 (Canada); Battaglia, Eric; Vignati, Davide A.L. [Laboratoire Interdisciplinaire des Environnements Continentaux, UMR 7360, Université de Lorraine and CNRS, 8 rue du Général Delestraint, 57070 Metz (France); Fortin, Claude, E-mail: claude.fortin@ete.inrs.ca [Institut National de la Recherche Scientifique, Centre Eau Terre Environnement (INRS-ETE), 490 rue de la Couronne, Québec (Québec) G1K 9A9 (Canada)

    2017-01-15

    Highlights: • C. reinhardtii accumulated similar levels of Cr(III) and Cr(VI). • The subcellular partitioning of Cr(III) and Cr(VI) was similar. • Cr(III) and Cr(VI) associated mainly with organelles and heat-stable proteins. • Metallomic analysis showed two main Cr-binding biomolecules after 72 h of exposure. - Abstract: Chromium occurs in aquatic environments under two main redox forms, namely Cr(III) and Cr(VI), with different geochemical and biochemical properties. Cr(VI) readily crosses biological membranes of living organisms and once inside the cells it undergoes a rapid reduction to Cr(III). The route of entry for the latter form is, however, poorly known. Using the radioactive tracer {sup 51}Cr we compared the accumulation (absorption and adsorption) of the two Cr forms by the green unicellular alga Chlamydomonas reinhardii after 1 h and 72 h of exposure to 100 nM of either Cr(III) or Cr(VI) at pH 7. Both Cr forms had similar accumulation, with a major part in the extracellular (adsorbed) fraction after 1 h and a major part of total accumulated Cr in the intracellular (absorbed) fraction after 72 h. We also investigated the intracellular partitioning of Cr using an operational fractionation scheme and found that both Cr forms had similar distributions among fractions: Cr was mostly associated with organelles (23 ± 12% after 1 h and 37 ± 7% after 72 h) and cytosolic heat-stable proteins and peptides (39 ± 18% after 1 h and 35 ± 3% after 72 h) fractions. Further investigations using a metallomic approach (SEC-ICP-MS) were performed with the heat-stable proteins and peptides fraction to compare the distribution of the two Cr forms among various biomolecules of this fraction. One Cr-binding biomolecule (∼28 kDa) appeared after 1 h of exposure for both Cr species. After 72 h another biomolecule of lower molecular weight (∼0.7 kDa) was involved in binding Cr and higher signal intensities were observed for Cr(VI) than for Cr(III). We show, for the

  18. CHROMIUM(VI REDUCTION BY A MIXED CULTURE OF SULFATE REDUCING BACTERIA DEVELOPED IN COLUMN REACTOR

    Directory of Open Access Journals (Sweden)

    Cynthia Henny

    2008-03-01

    Full Text Available A lactate enriched mixed sulfate reducing bacteria (SRB culture was examined for the reduction of Cr(VI in a continuous flow system. The influent was mineral salts media added with lactate and sulfate with amounts of 8 and 6 mM respectively as electron donor and electron acceptor. The SRB culture was allowed to stabilize in the column before adding the Cr(VI to the influent. Chromium and sulfate reduction and lactate oxidation were examined by measuring the concentrations of Cr(Vl, sulfate and lactate in the influent and the effluent over time. The experiment was discontinued when Cr(VI concentration in the effiuent was breakthrough. In the absence of Cr(VI, sulfate was not completely reduced in the column, although lactate was completely oxidized and acetate as an intermediate product was not often detected. Almost all of Cr(VI loaded was reduced in the column seeded with the SRB culture at influent Cr(VI concentrations of 192,385 and769 mM. There was no significant Cr(VI loss in the control column, indicating that Cr(VI removal was due to the reduction of Cr(VI to Cr (lll by the SRB culture. The instantaneous Cr(VI removal decreased to a minimum of 32%, 24 days after the influent Cr(VI concentration was increased to 1540 mM, ancl sulfate removal efficiency decreased to a minimum of 17%. The SRB population in the column decreased 100 days after C(VI was added to the column. The total mass of Cr(VI reduced was approximately 878 mmol out of 881 mmol of Cr(Vl loaded in 116 days. The results clearly show that our developed SRB culture could reduced Cr(Vl considerably.

  19. Porous p-NiO/n-Nb{sub 2}O{sub 5} nanocomposites prepared by an EISA route with enhanced photocatalytic activity in simultaneous Cr(VI) reduction and methyl orange decolorization under visible light irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Hashemzadeh, Fatemeh, E-mail: Fa.hashemzadeh@gmail.com [Young Researchers and Elite Clube, Marand Branch, Islamic Azad University, Marand (Iran, Islamic Republic of); Gaffarinejad, Ali, E-mail: Ghaffarinejad@iust.ac.ir [Department of Chemistry, Iran University of Science and Technology, Tehran 16846-13114 (Iran, Islamic Republic of); Rahimi, Rahmatollah, E-mail: Rahimi_Rah@iust.ac.ir [Department of Chemistry, Iran University of Science and Technology, Tehran 16846-13114 (Iran, Islamic Republic of)

    2015-04-09

    Highlights: • EISA synthesis of NiO/Nb{sub 2}O{sub 5} composites (NiNbx; x = Ni/Nb = 0.0, 0.4, 0.8, 1.2). • 200–400 nm extension in absorption edge to visible region compared to NiNb0.0. • Simultaneous Cr(VI)–MO redox photoreactions on NiNbx in visible light at pH 2. • NiNb0.4, the most active sample, due to low E{sub g} & e{sup −}–h{sup +} separation by p–n junction. • More efficiency of Cr(VI)–MO system than that of single ones, showing synergism effect. - Abstract: Porous NiO/Nb{sub 2}O{sub 5} nanocomposites with Ni/Nb molar ratio of 0.4, 0.8 and 1.2 have been obtained via the EISA route using P123 copolymer as organic template, and are assigned as NiNb0.4, NiNb0.8 and NiNb1.2, respectively. For comparison, pure Nb{sub 2}O{sub 5} sample assigned as NiNb0.0 was also synthesized by the same method. Structural and textural features of the as prepared samples were investigated by XRD, FTIR, FE-SEM, EDX, UV–vis DRS and BET techniques. The results indicated that the porous p-NiO/n-Nb{sub 2}O{sub 5} junction nanocomposites were formed and coupling of NiO with Nb{sub 2}O{sub 5} resulted a remarkable red shift in the optical response of the nanocomposite samples. The photocatalytic properties of the nanocomposite samples, and also synthesized pure Nb{sub 2}O{sub 5} (NiNb0.0) and commercial Nb{sub 2}O{sub 5} as reference catalysts were evaluated for the first time by simultaneous Cr(VI) reduction and MO decolorization in aqueous suspension under visible light irradiation at pH 2. NiNb0.4 was found to be the most active photocatalyst, which might be attributed to the extended absorption in the visible light region and the effective photogenerated electron–hole separation by the photosynergistic effects of the p-NiO/n-Nb{sub 2}O{sub 5} composite powder. The photocatalytic efficiency of the most active photocatalyst, NiNb0.4, was found to be rather low for either single Cr(VI) solution or single MO solution. However, the photocatalytic reduction of

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

    Science.gov (United States)

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

    2014-09-15

    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). Copyright © 2014 The Authors. Published by Elsevier B.V. All rights reserved.

  1. Chromium isotope inventory of Cr(VI)-polluted groundwaters at four industrial sites in Central Europe

    Science.gov (United States)

    Novak, Martin; Martinkova, Eva; Chrastny, Vladislav; Stepanova, Marketa; Curik, Jan; Szurmanova, Zdenka; Cron, Marcel; Tylcer, Jiri; Sebek, Ondrej

    2016-04-01

    Chromium is one of the most toxic elements, especially in its dissolved Cr(VI) form. In the Czech Republic (Central Europe), massive contamination of groundwater has been reported at more than 200 industrial operations. Under suitable conditions, i.e., low Eh, and high availability of reductive agents, Cr(VI) in groundwater may be spontaneously reduced to solid, largely non-toxic Cr(III). This process is associated with a Cr isotope fractionation, with the residual liquid Cr(VI) becoming enriched in the heavier isotope 53Cr. At industrial operations that have been closed and/or where no further leakage of Cr(VI) occurs, the contaminated groundwater plume may be viewed as a closed system. At such sites, an increasing degree of Cr(VI) reduction should result in an increasing del53/52Cr value of the residual liquid. Here we present del53/52Cr systematics at four contaminated Czech sites, focusing on groundwaters. At two of the four sites (Zlate Hory, Loucna) we were also able to analyze the source of contamination. Chromium in the electroplating solutes was isotopically relatively light, with del53/52Cr values VI) reduction may proceed at Zlate Hory and Loucna, where del53/52Cr(VI) values in groundwater were on average higher than those of the contamination source. At these two sites, our Cr isotope data are not consistent with the existing estimates of the amount of dissolved and precipitated Cr: The pool size of solid Cr(III) in the soil was estimated at 6600 and 500 kg at Zlate Hory and Loucna, respectively. At the same time, the pool size of dissolved Cr(VI) was estimated at 50 and 1.2 kg at Zlate Hory and Loucna, respectively. It follows that, at both sites, less than 1 % of the entire Cr that had leaked into the aquifer an a liquid form remained in the liquid form. If, indeed, most solid Cr now present in the saturated zone had undergone anaerobic reduction, we would expect much higher del53/52Cr values of the residual liquid Cr(VI) than those actually observed

  2. Finite difference simulation of biological chromium (VI) reduction in ...

    African Journals Online (AJOL)

    (VI) concentration profiles inside porous aquifer media columns. The model was thereafter used to calculate Cr(VI) removal rate for a range of Cr(VI) loadings. Internal concentration profiles were modelled against data collected from ...

  3. Applicability of a submersible microbial fuel cell for Cr(VI) detection in water.

    Science.gov (United States)

    Chung, Hyeonyong; Ju, Won Jung; Jho, Eun Hea; Nam, Kyoungphile

    2016-11-01

    Two-chamber microbial fuel cells (MFCs) were used to study the applicability of MFCs for hexavalent chromium (Cr(VI)) detection in water. The microbial acetate oxidation in the anode and the Cr(VI) reduction in the cathode together generated voltages, which were used to indicate the change in Cr(VI) concentrations of the cathode under varying conditions of pH, ionic strength, co-existing Fe(II) concentration, and organic matter concentration. The MFC-based Cr(VI) detector showed a significant change in voltage with increasing Cr(VI) concentration at pH 1 and 2, but not at higher pH conditions. The detector also successfully measured the changes in Cr(VI) concentration at a range of ionic strength (i.e., 10-300 mM), and in the presence of different concentrations of fulvic acid (0-50 mg/L), which was used as a surrogate of organic matters, without interference. The Cr(VI) detection was not interfered by the presence of Fe(II) at the Cr(VI)/Fe(II) ratio of 1:1 and 1:15, but it was interfered at higher ratios (i.e., 1:164 and 1:848). The detector could measure the Cr(VI) concentration from 0.1 to 15 mg/L at pH 2. Overall, the MFC-based Cr(VI) detector may be applied to meet the growing need of real-time Cr(VI) monitoring in water.

  4. Adsorption of Cu(II) and Cr(VI) ions by chitosan: Kinetics and ...

    African Journals Online (AJOL)

    drinie

    2001-01-01

    Jan 1, 2001 ... Current treatment for the removal of Cr. (VI) involves acid catalysed chemical reduction to Cr3+. The Cr3+ is then precipitated as hydroxide at alkaline conditions using either caustic or lime (Udaybhaskar et al., 1990). The presence of Cu (II) in wastewater is also a problem. Copper is used extensively by.

  5. Recovery of Cr as Cr(III) from Cr(VI)-contaminated kaolinite clay by electrokinetics coupled with a permeable reactive barrier.

    Science.gov (United States)

    Suzuki, Tasuma; Kawai, Katsunori; Moribe, Mai; Niinae, Masakazu

    2014-08-15

    Zero-valent iron (Fe(0)) and magnetite (Fe3O4) were investigated as potential reductants in an electrokinetic/permeable reactive barrier hybrid system (EK/PRB) for the recovery of Cr as Cr(III) from Cr(VI)-contaminated kaolinite. For the EK/Fe(0) PRB, regardless of the pH in the anode well, the system facilitated the reduction of Cr(VI) into Cr(III), but the recovery of the Cr(III) in the PRB was low. Conversely, the reduction of Cr(VI) occurred only in the PRB for the EK/Fe3O4 PRB. However, when the anode pH was not controlled and the soil pH values correspondingly decreased gradually from the anode side, a greater fraction of Cr(VI) sorbed onto the kaolinite; as a result, a lower amount of Cr(VI) migrated to the Fe3O4 PRB. In addition, it was found that the majority of Cr(VI) migrating to the Fe3O4 PRB retained its oxidation state without being converted into Cr(III). These two adverse effects were mitigated by maintaining the soil pH values at 6.8, but at the same time, 18% of Cr(VI) penetrated through the Fe3O4 PRB. The penetration of Cr(VI) through the Fe3O4 PRB was successfully prevented by increasing the reaction time through the introduction of a cation exchange membrane between the Fe3O4 PRB and the anode well. Copyright © 2014 Elsevier B.V. All rights reserved.

  6. Cr(III) reactivity and foot dermatitis in Cr(VI) positive patients

    DEFF Research Database (Denmark)

    Hansen, Malene Barré; Menné, Torkil; Johansen, Jeanne Duus

    2006-01-01

    Chromium allergy has become synonymous with Cr(VI) allergy. However, real exposure to chromium from leather products may include both Cr(III) and Cr(VI). In this study, we investigate the reactivity to both Cr(VI) and Cr(III) in consecutive patients to analyse the relation between foot eczema......(VI), of which 31 also had a positive Cr(III) reaction. No Cr(VI) negative patients had a positive reaction to Cr(III). An increased risk of foot dermatitis was found in Cr(VI) positive patients with a concomitant positive or doubtful reaction to Cr(III) compared with Cr(VI) positive patients with no reactions...... to Cr(III). The increased risk was not due to a higher degree of sensitivity to Cr(VI). Leather was reported most frequently as the suspected cause of chromium dermatitis (54%). However, Cr(VI) allergics having foot eczema and positive or doubtful Cr(III) reactions often had positive reactions to other...

  7. ADSORPTION OF Cr(VI ON BLACK WATER

    Directory of Open Access Journals (Sweden)

    Rasti Januarita

    2010-06-01

    Full Text Available The effect of initial concentration of Cr(VI on adsorption to black water of Gambut, District of Banjar, South Borneo has been investigated, as well as interaction between Cr(VI species and functional black water organic fraction. The initial work was optimization of Cr(VI determination using UV-Visible Spectrophotometry with diphenylcarbacide as complexing agent and preparation of black water using mixture of 2% HCl and 5% HF with HCl-HF ratio of 1 : 1 (v/v. The quantity of Cr(VI species adsorbed on black water was calculated by determining the amount of Cr(VI species in solution before and after interaction. The functional groups in interaction between Cr(VI species and black water organic fraction was studied qualitatively using infrared spectroscopy. The results showed that optimum condition for Cr(VI species analysis using UV-Visible spectrophotometry with diphenylcarbacide as complexing agent was at wave length of 540 nm, pH 1,5, 15 - 60 minutes at which complex remain stable, and minimum mol ratio of diphenylcarbacide : Cr(VI 45 : 1, and has a sensitivity of 1.134 mg/L and detection limit of 0.00495 mg/L. The analysis was not affected by the presence of Cr(III in concentration less than 40 times of Cr(VI concentration. After treatment with HCl-HF the quantity of black water organic fraction showing humic acid properties decreased 0,1998 percent. Organic fraction of black water used adsorpted Cr(VIwith capacity of 4,050 mg/g.   Keywords: Adsorption, Cr(VI, Black Water

  8. Simultaneously photocatalytic treatment of hexavalent chromium (Cr(VI)) and endocrine disrupting compounds (EDCs) using rotating reactor under solar irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Youngji [Korea Institute of Energy Research, New and Renewable Energy Research Division, Hydrogen Laboratory, 152 Gajeong-ro, Yuseong-gu, Daejeon 305-343 (Korea, Republic of); Yonsei University, Department of Chemical and Biomolecular Engineering, 134 Shinchon-dong, Seodaemun-gu, Seoul 120-749 (Korea, Republic of); Joo, Hyunku [Korea Institute of Energy Research, New and Renewable Energy Research Division, Hydrogen Laboratory, 152 Gajeong-ro, Yuseong-gu, Daejeon 305-343 (Korea, Republic of); Her, Namguk [Korea Army Academy at Young-Cheon, Department of Chemistry and Environmental Science, 135-1 Changhari, Kokyungmeon, Young-cheon, Gyeongbuk 770-849 (Korea, Republic of); Yoon, Yeomin [University of South Carolina, Department of Civil and Environmental Engineering, Columbia, SC 29208 (United States); Sohn, Jinsik [Kookmin University, School of Civil and Environmental Engineering, 77 Jeongneung-ro, Seongbuk-gu, Seoul 136-702 (Korea, Republic of); Kim, Sungpyo [Korea University, Department of Environmental Engineering, Sejong 339-700 (Korea, Republic of); Yoon, Jaekyung, E-mail: jyoon@kier.re.kr [Korea Institute of Energy Research, New and Renewable Energy Research Division, Hydrogen Laboratory, 152 Gajeong-ro, Yuseong-gu, Daejeon 305-343 (Korea, Republic of)

    2015-05-15

    Highlights: • Self-rotating reactor including TiO{sub 2} NTs is applied under solar irradiation. • Simultaneously photocatalysis of Cr(VI) and EDCs is observed to be up to 95%. • Photocatalytic reactions of Cr(VI) and EDCs are favorable under acidic pH. • Charge interaction and hole scavenge between TiO{sub 2} and pollutants are synergy factors. - Abstract: In this study, simultaneous treatments, reduction of hexavalent chromium (Cr(VI)) and oxidation of endocrine disrupting compounds (EDCs), such as bisphenol A (BPA), 17α-ethinyl estradiol (EE2) and 17β-estradiol (E2), were investigated with a rotating photocatalytic reactor including TiO{sub 2} nanotubes formed on titanium mesh substrates under solar UV irradiation. In the laboratory tests with a rotating type I reactor, synergy effects of the simultaneous photocatalytic reduction and oxidation of inorganic (Cr(VI)) and organic (BPA) pollutants were achieved. Particularly, the concurrent photocatalytic reduction of Cr(VI) and oxidation of BPA was higher under acidic conditions. The enhanced reaction efficiency of both pollutants was attributed to a stronger charge interaction between TiO{sub 2} nanotubes (positive charge) and the anionic form of Cr(VI) (negative charge), which are prevented recombination (electron–hole pair) by the hole scavenging effect of BPA. In the extended outdoor tests with a rotating type II reactor under solar irradiation, the experiment was extended to examine the simultaneous reduction of Cr(VI) in the presence of additional EDCs, such as EE2 and E2 as well as BPA. The findings showed that synergic effect of both photocatalytic reduction and oxidation was confirmed with single-component (Cr(VI) only), two-components (Cr(VI)/BPA, Cr(VI)/EE2, and Cr(VI)/E2), and four-components (Cr(VI)/BPA/EE2/E2) under various solar irradiation conditions.

  9. Reduction of trace quantities of chromium(VI by strong acids

    Directory of Open Access Journals (Sweden)

    Pezzin Sérgio H

    2004-01-01

    Full Text Available The chemical behavior of Cr(VI at low concentrations (10-4 to 10-7 mol L-1 in several strong acids was studied using high specific activity 51Cr(VI as a tracer. The speciation of the products from these systems was carried out by ion exchange chromatography with stepwise elution. The results show that trace quantities of Cr(VI, monitored by means of radiochromium (51Cr, are reduced in the presence of mineral acids such as perchloric, hydrochloric, hydrofluoric, sulfuric, nitric and trifluoromethanesulfonic acids, even in the absence of conventional reducing agents, producing different measureable Cr(III species, depending on the acid anion. Detailed studies of the reduction of low concentrations of Cr(VI with nitric acid have shown that the relative rate of reduction increases as the concentration of the acid increases or as the concentration of the Cr(VI decreases.

  10. Hydrothermal synthesis of α-Fe{sub 2}O{sub 3}/g-C{sub 3}N{sub 4} composite and its efficient photocatalytic reduction of Cr(VI) under visible light

    Energy Technology Data Exchange (ETDEWEB)

    Xiao, Dong [College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070 (China); College of Science, Huazhong Agricultural University, Wuhan 430070 (China); Dai, Ke, E-mail: dk@mail.hzau.edu.cn [College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070 (China); Qu, Yang; Yin, Yeping [College of Science, Huazhong Agricultural University, Wuhan 430070 (China); Chen, Hao, E-mail: hchenhao@mail.hzau.edu.cn [College of Science, Huazhong Agricultural University, Wuhan 430070 (China)

    2015-12-15

    Graphical abstract: - Highlights: • α-Fe{sub 2}O{sub 3} nanoparticles have been grown in-suit on the surface of g-C{sub 3}N{sub 4} nanosheets. • α-Fe{sub 2}O{sub 3}/g-C{sub 3}N{sub 4} shows enhanced photocatalytic activity for Cr(VI) reduction. • Z-scheme of α-Fe{sub 2}O{sub 3}/g-C{sub 3}N{sub 4} facilitates the separation and transfer of electron–hole. - Abstract: α-Fe{sub 2}O{sub 3}/g-C{sub 3}N{sub 4} composites were fabricated by a facile hydrothermal method. The prepared composites were characterized by XRD, XPS, TEM, DRS, PL and photoelectrochemical measurement. Under visible light irradiation, α-Fe{sub 2}O{sub 3}/g-C{sub 3}N{sub 4} composite displays higher photocatalytic activity than pure g-C{sub 3}N{sub 4} and α-Fe{sub 2}O{sub 3} for Cr(VI) reduction. The enhanced photocatalytic activity should be attributed to the well-matched band structure and intimate contact interfaces between g-C{sub 3}N{sub 4} and α-Fe{sub 2}O{sub 3}, which lead to the effective transfer and separation of the photogenerated charge carriers. The decoration of α-Fe{sub 2}O{sub 3} does not affect the morphology and size of g-C{sub 3}N{sub 4}. The lower photoluminescence intensity and higher photocurrent density indicate the effective transfer and separation of photogenerated charge carriers. α-Fe{sub 2}O{sub 3}/g-C{sub 3}N{sub 4} composite shows more intense optical absorption compared with pure g-C{sub 3}N{sub 4}. The addition of hole scavengers can greatly facilitate the photocatalytic reduction of Cr(VI) and the α-Fe{sub 2}O{sub 3}/g-C{sub 3}N{sub 4} composite shows excellent stability during the photocatalytic reduction of Cr(VI).

  11. Biogenic sulfides for sequestration of Cr (VI, COD and sulfate from synthetic wastewater

    Directory of Open Access Journals (Sweden)

    Anamika Verma

    2015-04-01

    Full Text Available The aim of this work is to explore the possibility of using mixed culture of mesophilic sulfate-reducing bacteria (SRB for retrieval of toxic and carcinogenic Cr (VI from synthetic solution. In order to treat Cr (VI containing wastewater effectively, SRB culture was adapted to 50 mg/L Cr (VI and maintained through repeated sub-culturing to enhance the growth and activity of SRB. Batch biosorption experiments were carried out in glass serum vials by cultured SRB, accomplishing the removal of 82.1% Cr (VI, 76.9% sulfate, 85.7% COD under the following optimized conditions: pH 7, hydraulic retention time (HRT 7 days, temperature 37 °C and initial Cr (VI concentration of 50 mg/L. Further sorption experiments were conducted on synthetic wastewater under optimal operational conditions and resulted in 89.2% Cr (VI, 81.9% COD and 95.3% sulfate reduction from simulated wastewater. The results of this work contributed to a better understanding of metal uptake by biogenic sulfides and would be beneficial in the development of potential biosorbents that possess high capacities for Cr (VI uptake from aqueous environments.

  12. Theophylline-assisted, eco-friendly synthesis of PtAu nanospheres at reduced graphene oxide with enhanced catalytic activity towards Cr(VI) reduction.

    Science.gov (United States)

    Hu, Ling-Ya; Chen, Li-Xian; Liu, Meng-Ting; Wang, Ai-Jun; Wu, Lan-Ju; Feng, Jiu-Ju

    2017-05-01

    Theophylline as a naturally alkaloid is commonly employed to treat asthma and chronic obstructive pulmonary disorder. Herein, a facile theophylline-assisted green approach was firstly developed for synthesis of PtAu nanospheres/reduced graphene oxide (PtAu NSs/rGO), without any surfactant, polymer, or seed involved. The obtained nanocomposites were applied for the catalytic reduction and removal of highly toxic chromium (VI) using formic acid as a model reductant at 50°C, showing the significantly enhanced catalytic activity and improved recyclability when compared with commercial Pt/C (50%) and home-made Au nanocrystals supported rGO (Au NCs/rGO). It demonstrates great potential applications of the catalyst in wastewater treatment and environmental protection. The eco-friendly route provides a new platform to fabricate other catalysts with enhanced catalytic activity. Copyright © 2016 Elsevier Inc. All rights reserved.

  13. Cr(VI) and Cr(III)-Based Conversion Coatings on Zinc

    NARCIS (Netherlands)

    Zhang, X.

    2005-01-01

    With the aims of understanding the protective mechanism of chromate conversion coatings and developing alternatives to chromate treatments, the physical natures and corrosion properties of Cr(VI) and Cr(III) treated zinc have been investigated in this work. The Cr(VI) treatments were carried out in

  14. New low cost sorbents for Cr(VI – batch and column experiments

    Directory of Open Access Journals (Sweden)

    Šillerová H.

    2013-04-01

    Full Text Available The use of agricultural byproducts and industrial biowaste materials has been shown to be an attractive technique for removing Cr(VI from contaminated waste waters. In this study, used brewers draff, peat moss, sawdust, grape stalks and husks were investigated as novel biosorbents for Cr(VI. The material was tested in two different modifications. The material was dried, cut and sieved and part of it was subjected to acid (2 M H2SO4 and alkali (0.5 M NaOH pre-treatments to remove starch, proteins and sugars. Fourier transform infrared rays analysis on solid phase (FTIR-ATR was used to determine the main functional groups that might control the metal uptake. Batch experiments were performed at different pH values (3, 4.5, 6 and at various initial concentration of Cr(VI (25–2012;250 mg L−1. Two equilibrium empirical models, Langmuir and Freundlich, were used to describe Cr(VI adsorption. In order to identify possible reduction processes, ion exchange separation on the AG1-X8 resin was used to separate the anionic Cr(VI and the reduced cationic Cr(III from the aqueous phase after biosorption. As expected, Cr(VI removal was pH-dependent and fitted well both the Langmuir and Freundlich isotherm models. The ion exchange separation showed that Cr(VI reduction had occurred in the solution during biosorption. The efficiency of draff as a biosorbent was comparable (or even higher to highly organic materials (e.g., composted peat showing its potential application for Cr(VI decontamination.

  15. Characterizing toxic Cr(VI) contamination in chromite mine overburden dump and its bacterial remediation.

    Science.gov (United States)

    Dhal, B; Das, N N; Thatoi, H N; Pandey, B D

    2013-09-15

    Cr(VI) generated due to natural oxidation of chromite mineral present in chromite mine overburden (COB) dumps of Sukinda, India, has been characterized by different physico-chemical methods. The Cr(VI) was found to be associated with goethite matrix at a contamination level of 500 mg Cr(VI)kg(-1) of COB. Bacillus sp. isolated from the overburden sample exhibiting high tolerance to the hexavalent chromium, was used for the remediation of Cr(VI) in the overburden. The process was optimized while varying the parameters such as pH (2-9), pulp density (10-60%) and temperature (25-40 °C). Optimal reduction of more than 98% of Cr(VI) in the COB sample was achieved in 16 h at pH∼7.0 and 60% pulp density with the Bacillus sp. (4.05 × 10(7)cells mL(-1)) in absence of media. The exponential rate equation yielded rate constant value of 2.14 × 10(-1)h(-1) at 60% pulp density. The mode of bio-reduction of Cr(VI) in the overburden sample was established by FT-IR, XRD, EPMA and SEM-EDS studies. Copyright © 2013 Elsevier B.V. All rights reserved.

  16. The roles of polycarboxylates in Cr(VI)/sulfite reaction system: Involvement of reactive oxygen species and intramolecular electron transfer

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, Bo, E-mail: bjiang86upc@163.com [State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Qingdao 266580, Shandong (China); School of Environmental and Municipal Engineering, Qingdao University of Technology, Qingdao 266033 (China); Wang, Xianli; Liu, Yukun [State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Qingdao 266580, Shandong (China); Wang, Zhaohui [College of Environmental Science and Engineering, Donghua University, Shanghai 201620 (China); Southern Cross GeoScience, Southern Cross University, Lismore, NSW 2480 (Australia); Zheng, Jingtang, E-mail: jtzheng03@163.com [State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Qingdao 266580, Shandong (China); Wu, Mingbo, E-mail: wumb@upc.edu.cn [State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Qingdao 266580, Shandong (China)

    2016-03-05

    Highlights: • The formations of SO{sub 4}·{sup −} and OH·, involve in Cr(VI) reduction induced by S(IV). • Affinity of polycarboxylate to Cr(VI) accelerates Cr(VI) reduction rate. • Polycarboxylates can act as electron donors for Cr(VI) reduction retrenching S(IV). • Only oxalate can enhance the formations of SO{sub 4}·{sup −} and OH· in Cr(VI)/S(IV) system. - Abstract: In this study, the effects of polycarboxylates on both Cr(VI) reduction and S(IV) consumption in Cr(VI)/S(IV) system was investigated in acidic solution. Under aerobic condition, the productions of reactive oxygen species (ROS), i.e., SO{sub 4}·{sup −} and OH·, have been confirmed in S(IV) reducing Cr(VI) process by using electron spin resonance and fluorescence spectrum techniques, leading to the excess consumption of S(IV). However, when polycarboxylates (oxalic, citric, malic and tartaric acid) were present in Cr(VI)/S(IV) system, the affinity of polycarboxylates to CrSO{sub 6}{sup 2−} can greatly promote the reduction of Cr(VI) via expanding the coordination of Cr(VI) species from tetrahedron to hexahedron. Besides, as alternatives to S(IV), these polycarboxylates can also act as electron donors for Cr(VI) reduction via intramolecular electron transfer reaction, which is dependent on the energies of the highest occupied molecular orbital of these polycarboxylates. Notably, the variant electron donating capacity of these polycarboxylates resulted in different yield of ROS and therefore the oxidation efficiencies of other pollutants, e.g., rhodamine B and As(III). Generally, this study does not only shed light on the mechanism of S(IV) reducing Cr(VI) process mediated by polycarboxylates, but also provides an escalated, cost-effective and green strategy for the remediation of Cr(VI) using sulfite as a reductant.

  17. Study of reduction of chromium (VI by calcium polysulfide using spectrophotometric method

    Directory of Open Access Journals (Sweden)

    Batukhan Tatykaev

    2013-05-01

    Full Text Available The paper presents  the results of the study on reduction  of  Cr2O72-   to   Cr3 +  by aqueous solution of calcium polysulfide  using spectrophotometric method. Concentrations  of Cr (VI were determined on the basis of the absorption spectrum at the wavelength range 350 - 372 nm. The change of the concentration of Cr (VI during on reduction by calcium polysulfide has been shown.  The influence of pH on the rate of reducing of Cr (VI to Cr (III was considered: the rate of reducing of hexavalent chromium decreases with increasing pH. The data obtained show that recycling Cr (VI in industrial scale potentially effective at  the pH = 5.

  18. Determination of Cr(III, Cr(VI and total chromium in atmospheric aerosol samples

    Directory of Open Access Journals (Sweden)

    Catrambone M.

    2013-04-01

    Full Text Available This study addresses the optimization and validation of an analytical method based on the ultrasound-assisted extraction of soluble Cr from atmospheric particulate matter (PM and subsequent determination of Cr(III and Cr(VI by catalytic adsorptive stripping voltammetry (CAdSV by using diethylenetriammino pentaacetic acid (DTPA as complexing agent in the presence of nitrate. We evaluated the influence of various filter materials and of extracting conditions and validated the method on both reference material and real PM10 samples. The accuracy of total extractable Cr determination was checked by parallel ICP-OES measurements. The determination of total chromium was performed by ED-XRF. Results of field campaigns carried out in two industrial areas (North Italy and Tunis and at a peri-urban site near Rome are reported. At the peri-urban site, the total Cr concentration in PM10 ranged from 2 to 5 ng/m3, with a soluble fraction of 5-13%, and Cr(VI concentration was always below the detection limits (50 pg/m3. In the industrial area of Northern Italy, total Cr concentration ranged between 6 and 11 ng/m3, the soluble fraction was about 11-28% and detectable amounts of Cr(VI were found, with a Cr(VI/Cr(III ratio ranging from 0.5 to 2.5. A further increase of Cr(VI concentration was evidenced at the industrial site of Tunis, where the total Cr concentration ranged from 6 to 26 ng/m3, with a soluble fraction accounting for about 8-44% and a Cr(VI/Cr(III ranging from 1.6 to 3.6. The results of size-segregated samples, collected in Northen Italy by a 10-stage cascade impactor, indicate a relevant fine fraction of Cr(VI, with Cr(VI/Cr(III ratios increasing with the decrease of particle size.

  19. The role of sulfide in the immobilization of Cr(VI) in fly ash geopolymers

    Energy Technology Data Exchange (ETDEWEB)

    Jianguo Zhang; John L. Provis; Dingwu Feng; Jannie S.J. van Deventer [University of Melbourne, Melbourne, Vic. (Australia). Department of Chemical and Biomolecular Engineering

    2008-05-15

    The use of fly ash-based geopolymer binders to immobilize chromium is investigated in detail, with particular regard to the role of the sulfide ion as a reductant for Cr(VI) treatment. In the absence of sulfide, Cr added as Cr(VI) is highly leachable. However, addition of a small quantity of Na{sub 2}S reduces the Cr to Cr(III), and enables leaching efficiencies in excess of 99.9% to be reached after 90 days' exposure to deionized water, Na{sub 2}CO{sub 3} or MgSO{sub 4} solutions. Leaching in H{sub 2}SO{sub 4} is somewhat greater than this, due most probably to the oxidation of the Cr(III) present. Addition of the Cr(VI) as a highly soluble salt is preferable to its addition as a sparingly soluble salt, because a higher salt solubility means the Cr(VI) is more available for reduction prior to geopolymeric setting. The potential value of geopolymer technology as an immobilization process for problematic heavy metal waste streams is highlighted by these results, and the need for a full understanding of binder chemistry in any immobilization system outlined.

  20. Chromium(VI) removal via reduction-sorption on bi-functional silica adsorbents.

    Science.gov (United States)

    Zaitseva, Nataliya; Zaitsev, Vladimir; Walcarius, Alain

    2013-04-15

    Organically-modified silica gels bearing mercaptopropyl and ethylenediaminetriacetate groups (SiO2-SH/ED3A) have been used for reduction and subsequent sequestration of Cr(VI) species. The uptake mechanism involves Cr(VI) reduction by thiol groups (SH) and further immobilization of the so-generated Cr(III) species via complexation to the ethylenediaminetriacetate moieties (ED3A). The most appropriate pH range (1-3) for complete Cr(VI) reduction-sorption by SiO2-SH/ED3A originates from the balance between full reduction of Cr(VI) by SH, requiring low pH values, and quantitative complexation of Cr(III) by ED3A, which is favored in less acidic media. Such bi-functional adsorbents are considerably more effective at removal of Cr(VI) than those simply modified with thiol groups alone. The whole reduction-sorption process was characterized by fast kinetics, thus permitting efficient use of the SiO2-SH/ED3A adsorbent in dynamic conditions (column experiments). Monitoring the amount of immobilized chromium species on the solid was achieved using X-ray fluorescence spectroscopy and UV-vis spectroscopy. Studying the influence of ionic strength and presence of heavy metals revealed few interference on Cr(VI) removal. Copyright © 2013 Elsevier B.V. All rights reserved.

  1. Biological Cr(VI) removal using bio-filters and constructed wetlands.

    Science.gov (United States)

    Michailides, Michail K; Sultana, Mar-Yam; Tekerlekopoulou, Athanasia G; Akratos, Christos S; Vayenas, Dimitrios V

    2013-01-01

    The bioreduction of hexavalent chromium from aqueous solution was carried out using suspended growth and packed-bed reactors under a draw-fill operating mode, and horizontal subsurface constructed wetlands. Reactors were inoculated with industrial sludge from the Hellenic Aerospace Industry using sugar as substrate. In the suspended growth reactors, the maximum Cr(VI) reduction rate (about 2 mg/L h) was achieved for an initial concentration of 12.85 mg/L, while in the attached growth reactors, a similar reduction rate was achieved even with high initial concentrations (109 mg/L), thus confirming the advantage of these systems. Two horizontal subsurface constructed wetlands (CWs) pilot-scale units were also built and operated. The units contained fine gravel. One unit was planted with common reeds and one was kept unplanted. The mean influent concentrations of Cr(VI) were 5.61 and 5.47 mg/L for the planted and unplanted units, respectively. The performance of the planted CW units was very effective as mean Cr(VI) removal efficiency was 85% and efficiency maximum reached 100%. On the contrary, the unplanted CW achieved very low Cr(VI) removal with a mean value of 26%. Both attached growth reactors and CWs proved efficient and viable means for Cr(VI) reduction.

  2. Integrated Cr(VI) removal using constructed wetlands and composting.

    Science.gov (United States)

    Sultana, Mar-Yam; Chowdhury, Abu Khayer Md Muktadirul Bari; Michailides, Michail K; Akratos, Christos S; Tekerlekopoulou, Athanasia G; Vayenas, Dimitrios V

    2015-01-08

    The present work was conducted to study integrated chromium removal from aqueous solutions in horizontal subsurface (HSF) constructed wetlands. Two pilot-scale HSF constructed wetlands (CWs) units were built and operated. One unit was planted with common reeds (Phragmites australis) and one was kept unplanted. Influent concentrations of Cr(VI) ranged from 0.5 to 10mg/L. The effect of temperature and hydraulic residence time (8-0.5 days) on Cr(VI) removal were studied. Temperature was proved to affect Cr(VI) removal in both units. In the planted unit maximum Cr(VI) removal efficiencies of 100% were recorded at HRT's of 1 day with Cr(VI) concentrations of 5, 2.5 and 1mg/L, while a significantly lower removal rate was recorded in the unplanted unit. Harvested reed biomass from the CWs was co-composted with olive mill wastes. The final product had excellent physicochemical characteristics (C/N: 14.1-14.7, germination index (GI): 145-157%, Cr: 8-10mg/kg dry mass), fulfills EU requirements and can be used as a fertilizer in organic farming. Copyright © 2014 Elsevier B.V. All rights reserved.

  3. Natural attenuation of Cr(VI) contaminated groundwater at two industrial sites in the eastern U.S.A.: A Cr isotope study

    Science.gov (United States)

    Novak, Martin; Hellerich, Lucas A.; Sebek, Ondrej; Andronikov, Alexandre; Chrastny, Vladislav; Curik, Jan; Stepanova, Marketa; Pacherova, Petra; Martinkova, Eva; Prechova, Eva; Veselovsky, Frantisek

    2017-04-01

    Hexavalent chromium [Cr(VI)], found in various compartments of the environment, has generated much interest due to its extreme toxicity and mobility. We studied natural attenuation of Cr(VI)-contaminated groundwater at one site in Connecticut (site A), and one site in New Jersey (site B), U.S.A. Shallow groundwater was contaminated by electroplating solutions at site A, and by water-soluble chromite ore-processing residues at site B. Site A had lower Cr(VI) concentrations of less than 1 mg L-1 in comparison to site B (200 mg L-1). Site A also had lower mean del53Cr values (1.4 per mil) than site B (2.9 per mil). Chromium isotope composition of the pollution sources (plating bath, ore) was known (del53Cr of 0.0 to 0.2 per mil). The positive Cr isotope shift from the pollution source Cr(VI) to groundwater Cr(VI) at both sites indicated that spontaneous Cr(VI) reduction to insoluble Cr(III) is under way. This process is removing toxicity from the groundwater. Del53Cr values of groundwater were strongly positively correlated with the concentration of dissolved organic carbon (DOC), but not with divalent Fe and Mn, indicating that DOC may be the main Cr-reducing agent. A Rayleigh model indicated that 30 and 57 % of the original contaminant may have been removed from the groundwater by natural attenuation at site A and B, respectively. Interestingly, del53Cr values of the residual Cr(VI) in the groundwater at site A decreased significantly over the past 15 years, during which the water is being extracted for chemical treatment. At present, older, less fractionated Cr(VI) may be extracted at site A.

  4. Cr(VI) generation during sample preparation of solid samples – A ...

    African Journals Online (AJOL)

    2009-05-15

    ) extraction should be to quantitatively extract Cr(VI), without inducing changes in speciation, i.e.. Cr(III)/Cr(VI) inter-conversions (Pettine and Capri, 2005). The reviews by Ashley et al. (2003), Broadhurst and Maizda.

  5. New generation ion-imprinted nanocarrier for removal of Cr(VI) from wastewater

    Energy Technology Data Exchange (ETDEWEB)

    Uygun, Murat, E-mail: muygun@adu.edu.tr [Adnan Menderes University, Kocarl Latin-Small-Letter-Dotless-I Vocational and Training School (Turkey); Feyzioglu, Esra; Oezcal Latin-Small-Letter-Dotless-I skan, Emir; Caka, Mueserref; Ergen, Aygen; Akgoel, Sinan [Ege University, Department of Biochemistry, Faculty of Science (Turkey); Denizli, Adil [Hacettepe University, Department of Chemistry, Faculty of Science (Turkey)

    2013-08-15

    The purpose of this study was to prepare a novel ion-imprinted nanoparticle to remove Cr(VI) ions from waste water. For this, Cr(VI) ions were complexed with 2-methacryloylamido histidine (MAH) and then Cr(VI)-imprinted poly(HEMAH) nanoparticles were synthesized by surfactant-free emulsion polymerization technique. The templates, Cr(VI) ions, were removed from the nanoparticles using 0.1 M of HNO{sub 3} solution. The specific surface area of the Cr(VI)-imprinted poly(HEMAH) nanoparticles was found to be 1,397.85 m{sup 2}/g, and the particle size was calculated as 155.3 nm. These Cr(VI)-imprinted nanoparticles were used for the adsorption/desorption of Cr(VI) ions from its aqueous solutions. The effects of initial Cr(VI) concentration and medium pH on the Cr(VI) adsorption capacity were also studied. The maximum adsorbed amount of Cr(VI) on the imprinted nanoparticles was found to be 3,830.58 mg/g nanoparticle in pH 4.0. In order to investigate the selectivity of the imprinted nanoparticle, adsorption studies were repeated using Cr(III) ions. The selectivity results demonstrated that Cr(VI)-imprinted poly(HEMAH) nanoparticles showed high affinity for the Cr(VI) ions than Cr(III). The Cr(VI)-imprinted nanoparticles were used several times without decreasing their Cr(VI) adsorption capacities.

  6. Controllable one-pot synthesis of various one-dimensional Bi{sub 2}S{sub 3} nanostructures and their enhanced visible-light-driven photocatalytic reduction of Cr(VI)

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Enlai; Gao, Xuehui; Etogo, Atangana; Xie, Yunlong [Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Institute of Physical Chemistry, Zhejiang Normal University, Jinhua 321004 (China); Zhong, Yijun, E-mail: yjzhong@zjnu.cn [College of Chemistry and Life Sciences, Zhejiang Normal University, Jinhua 321004 (China); Hu, Yong, E-mail: yonghu@zjnu.edu.cn [Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Institute of Physical Chemistry, Zhejiang Normal University, Jinhua 321004 (China)

    2014-10-25

    Highlights: • 1D Bi{sub 2}S{sub 3} nanostructures were prepared by a facile ethanol-assisted one-pot reaction. • The size and morphology of the products can be conveniently varied. • The sulfur source plays a crucial role in determining the morphologies of products. • 1D Bi{sub 2}S{sub 3} nanostructures exhibit enhanced photocatalytic reduction of Cr(VI). • Bi{sub 2}S{sub 3} nanowires exhibit the highest photoreduction activity among three samples. - Abstract: One-dimensional (1D) Bi{sub 2}S{sub 3} nanostructures with various morphologies, including nanowires, nanorods, and nanotubes, have been successfully synthesized through a facile ethanol-assisted one-pot reaction. It is found that the size, morphology and structure of the products can be conveniently varied or controlled by simply adjusting the volume ratio of ethanol and water in the reaction system. Further experimental results indicate that sulfur source also plays the other crucial role in determining the product morphology. The synthetic strategy developed in this work is highly efficient in producing 1D Bi{sub 2}S{sub 3} nanostructures with high quality and large quantity. Photocatalysis experiments show the as-prepared 1D Bi{sub 2}S{sub 3} nanostructures possess significantly enhanced photocatalytic reduction of Cr(VI) when exposed to visible light irradiation. Especially, Bi{sub 2}S{sub 3} nanowires exhibit the highest photocatalytic activity and can be used repeatedly after washed with dilute HCl.

  7. TiO2@Pt@CeO2 nanocomposite as a bifunctional catalyst for enhancing photo-reduction of Cr (VI) and photo-oxidation of benzyl alcohol.

    Science.gov (United States)

    Li, Shunxing; Cai, Jiabai; Wu, Xueqing; Liu, Biwen; Chen, Qiaoying; Li, Yuehai; Zheng, Fengying

    2018-03-15

    An solar-light-driven and bifunctional photocatalyst was designed for photo-reduction of Cr(VI) and selective photo-oxidation of benzyl alcohol into benzaldehyde in the presence of water under ambient conditions. Double-shelled and sandwiched TiO2@Pt@CeO2 hollow spheres were prepared by using functionalized polystyrene spheres, sol-gel, hydrothermal reaction, and calcination. The Pt nanoparticles (NPs) were controllably loaded between the TiO2 shell and CeO2 shell. Under solar-light irradiation, the photo-reduction rate of Cr(VI) (μmol h-1) was in the order of TiO2@Pt@CeO2 (1.901) > TiO2@CeO2 (1.424) > TiO2 (1.040) > CeO2 (0.992). Among the above-mentioned photocatalysts, the conversion rate of benzyl alcohol for TiO2@Pt@CeO2 was also the best. These results were attributed to the combination of TiO2 and CeO2 as photocatalyst and oxygen buffer, the double-shelled and sandwiched nanostructure, and the addition of Pt NPs as cocatalyst and electron trap site, which could store and shuttle photo-generated electrons, reduce the recombination of the electron-hole, and then enhance photo-generation of active radicals. This conclusion was verified by the electron paramagnetic resonance (EPR) spectroscopy. Considering the versatile combination of photocatalyst, oxygen buffer and cocatalyst, this work could provide new insights into the design of high-performance bifunctional photocatalysts for heavy metal removal and selective synthesis. Copyright © 2017 Elsevier B.V. All rights reserved.

  8. Cr(VI) removal from aqueous systems using pyrite as the reducing agent: batch, spectroscopic and column experiments.

    Science.gov (United States)

    Kantar, Cetin; Ari, Cihan; Keskin, Selda; Dogaroglu, Zeynep Gorkem; Karadeniz, Aykut; Alten, Akin

    2015-03-01

    Laboratory batch and column experiments, in conjunction with geochemical calculations and spectroscopic analysis, were performed to better understand reaction mechanisms and kinetics associated with Cr(VI) removal from aqueous systems using pyrite as the reactive material under both static and dynamic flow conditions similar to those observed in in situ permeable reactive barriers (PRBs). The X-ray photoelectron spectroscopy (XPS) and geochemical calculations suggest that the Cr(VI) removal by pyrite occurred due to the reduction of Cr(VI) to Cr(III), coupled with the oxidation of Fe(II) to Fe(III) and S2(2-) to SO4(2-) at the pyrite surface. Zeta potential measurements indicate that although the pyrite surface was negatively charged under a wide pH range in the absence of Cr(VI), it behaved more like a "metal oxide" surface with the surface potential shifting from positive to negative values at pH values >pH 6 in the presence of Cr(VI). Batch experiments show that increasing solution pH led to a significant decrease in Cr(VI) removal. The decrease in Cr(VI) removal at high Cr(VI) concentrations and pH values can be explained through the precipitation of sparingly soluble Cr(OH)(3(s)), Fe(OH)(3(s)) and Fe(III)-Cr(III) (oxy) hydroxides onto pyrite surface which may, then, lead to surface passivation for further Cr(VI) reduction. Batch results also suggest that the reaction kinetics follow a first order model with rate constants decreasing with increasing solution pH, indicating proton consumption during Cr(VI) reduction by pyrite. Column experiments indicate that nearly 100% of total Fe in the column effluent was in the form of Fe(II) species with a [SO4(2-)]/[Fe(2+)] stoichiometric ratio of 2.04, indicating that the reduction of Cr(VI) by pyrite produced about 2 mol of sulfate per mole of Fe (II) release under excess surface sites relative to Cr(VI) concentration. Column experiments provide further evidence on the accumulation of oxidation products which

  9. Cr(VI) removal from aqueous systems using pyrite as the reducing agent: Batch, spectroscopic and column experiments

    Science.gov (United States)

    Kantar, Cetin; Ari, Cihan; Keskin, Selda; Dogaroglu, Zeynep Gorkem; Karadeniz, Aykut; Alten, Akin

    2015-03-01

    Laboratory batch and column experiments, in conjunction with geochemical calculations and spectroscopic analysis, were performed to better understand reaction mechanisms and kinetics associated with Cr(VI) removal from aqueous systems using pyrite as the reactive material under both static and dynamic flow conditions similar to those observed in in situ permeable reactive barriers (PRBs). The X-ray photoelectron spectroscopy (XPS) and geochemical calculations suggest that the Cr(VI) removal by pyrite occurred due to the reduction of Cr(VI) to Cr(III), coupled with the oxidation of Fe(II) to Fe(III) and S22 - to SO42 - at the pyrite surface. Zeta potential measurements indicate that although the pyrite surface was negatively charged under a wide pH range in the absence of Cr(VI), it behaved more like a "metal oxide" surface with the surface potential shifting from positive to negative values at pH values > pH 6 in the presence of Cr(VI). Batch experiments show that increasing solution pH led to a significant decrease in Cr(VI) removal. The decrease in Cr(VI) removal at high Cr(VI) concentrations and pH values can be explained through the precipitation of sparingly soluble Cr(OH)3(s), Fe(OH)3(s) and Fe(III)-Cr(III) (oxy) hydroxides onto pyrite surface which may, then, lead to surface passivation for further Cr(VI) reduction. Batch results also suggest that the reaction kinetics follow a first order model with rate constants decreasing with increasing solution pH, indicating proton consumption during Cr(VI) reduction by pyrite. Column experiments indicate that nearly 100% of total Fe in the column effluent was in the form of Fe(II) species with a [SO42 -]/[Fe2 +] stoichiometric ratio of 2.04, indicating that the reduction of Cr(VI) by pyrite produced about 2 mol of sulfate per mole of Fe (II) release under excess surface sites relative to Cr(VI) concentration. Column experiments provide further evidence on the accumulation of oxidation products which consequently led

  10. Enhanced removal of toxic Cr(VI) in tannery wastewater by photoelectrocatalysis with synthetic TiO2 hollow spheres

    Science.gov (United States)

    Zhao, Yang; Chang, Wenkai; Huang, Zhiding; Feng, Xugen; Ma, Lin; Qi, Xiaoxia; Li, Zenghe

    2017-05-01

    Owing to the acute toxicity and mobility, the Cr(VI) in tannery wastewater is a huge threat to biological and environmental systems. Herein, an effective photoelectrocatalytic reduction of Cr(VI) was carried out by applying electric field to photocatalysis of as-prepared TiO2 spheres. The synthesis of spherical TiO2 catalytic materials with hollow structure and high surface areas was based on a self-assembly process induced by a mixture of organic acetic acid and ethanol. The possible formation mechanism of TiO2 spheres was proposed and verified by acid concentration-dependent and temperature-dependent experiments. It was found that the reaction rate constant of photoelectrocatalytic reduction of Cr(VI) exhibited an almost 3 fold improvement (0.0362 min-1) as compared to that of photocatalysis (0.0126 min-1). As a result, the mechanism of photoelectrocatalytic reduction of Cr(VI) was described according to the simultaneous determination of Cr(VI), Cr(III) and total Cr in the system. In addition, the effect of pH value and voltage of potential were also discussed. Moreover, this photoelectrocatalysis with TiO2 hollow spheres exhibited excellent activity for reduction of Cr(VI) in actual tannery wastewater produced from three different tanning procedures. These attributes suggest that this photoelectrocatalysis has strong potential applications in the treatment of tannery pollutants.

  11. Enhanced Performance for Treatment of Cr (VI-Containing Wastewater by Microbial Fuel Cells with Natural Pyrrhotite-Coated Cathode

    Directory of Open Access Journals (Sweden)

    Junxian Shi

    2017-12-01

    Full Text Available Here we reported the investigation of enhanced performance for the removal of hexavalent chromium (Cr (VI by a new microbial fuel cell (MFC with natural pyrrhotite-coated cathode. By comparisons of the graphite-cathode, the MFCs equipped with a pyrrhotite-coated cathode generated the maximum power density of 45.4 mW·m−2 that was 1.3 times higher than that of with bare graphite cathode (35.5 mW·m−2. Moreover, the Cr (VI removal efficiency of 97.5% achieved after 4.5 h compared with only 46.1% by graphite cathode MFC. In addition, Cr (VI removal rate with different initial Cr (VI concentrations for 10 mg/L and 30 mg/L was investigated and a decreased removal percentage with increasing Cr (VI concentration was observed. Batches of experiments of different pH values from 3.0 to 9.0 in catholyte were carried out to optimize system performance. The complete Cr (VI removal was achieved at pH 3.0 and 99.59% of Cr (VI was removed after 10.5 h, which met the requirement of the Cr (VI National Emission Standard. When the value of pH was decreasing, the removal rate was obviously increased and Cr (VI could be removed successfully with a broad pH range indicating pyrrhotite-coated cathode MFC had more extensive usage scope. Furthermore, cathode treatment products were studied by X-ray photoelectron spectroscopy (XPS, Cr2O3, Cr (III-acetate were detected on the cathode by the XPS Cr2p spectra and no Cr (VI founded, indicating that the Cr on the surface of cathode was Cr (III and Cr (VI were reduced. On cathode, pyrrhotite not only played a significant role for catalyst of MFCs, but also acted as reactive sites for Cr (VI reduction. Our research demonstrated that pyrrhotite, an earth-abundant and low-cost natural mineral was promised as an effective cathode material. Which had great potential applications in MFCs for reduction of wastewater containing heavy metals and other environmental contaminants in the future.

  12. The use of sulphuric acid-carbonization products of sugar beet pulp in Cr(VI) removal.

    Science.gov (United States)

    Altundogan, H Soner; Bahar, Nurdan; Mujde, Buket; Tumen, Fikret

    2007-06-01

    A carbon rich adsorbent prepared from the reaction of sugar beet pulp with sulphuric acid and gas formed during carbonization process have been studied for Cr(VI) removal from aqueous solutions. The SO(2) rich gas was shown to be an excellent Cr(VI) reductant. The equilibrium and kinetic studies were conducted by using the carbonaceous adsorbent derived from sugar beet pulp. The lower pH favoured Cr(VI) adsorption but substantial Cr(VI) reduction was observed. The Langmuir and Freundlich isotherm models were applied and the Langmuir model best fit the equilibrium isotherm data. The maximum adsorption capacity of chromium calculated from Langmuir isotherm is about 24 mgg(-1) for 25 degrees C. The adsorption of Cr(VI) is an endothermic process and follows the pseudo-second-order rate kinetics. The sulphuric acid-carbonization is an economical method for particularly chromium removal because the gas generated during carbonization exhibits good Cr(VI) reduction properties and carbonaceous material obtained is an efficient Cr(VI) adsorbent.

  13. Deferoxamine pretreatment prevents Cr(VI)-induced nephrotoxicity and oxidant stress: role of Cr(VI) chelation.

    Science.gov (United States)

    Molina-Jijón, Eduardo; Zarco-Márquez, Guillermo; Medina-Campos, Omar Noel; Zataraín-Barrón, Zyanya Lucía; Hernández-Pando, Rogelio; Pinzón, Enrique; Zavaleta, Rosa Marina; Tapia, Edilia; Pedraza-Chaverri, José

    2012-01-27

    Deferoxamine (DFO) is a recognized iron chelator which has been shown to exert nephroprotection in models of toxic nephropathies. In the present work the potential protective effects of DFO against Cr(VI)-induced nephrotoxicity and oxidant stress were evaluated. Rats were injected with a single injection (15mg/kg, s.c.) of potassium dichromate (K(2)Cr(2)O(7)). DFO was given as a single i.p. injection 30min before K(2)Cr(2)O(7) administration at three different doses (100, 200 and 400mg/kg). It was found that DFO pretreatment attenuated, in a dose-dependent way, K(2)Cr(2)O(7)-induced renal dysfunction and structural alterations evaluated by serum creatinine, blood urea nitrogen, creatinine clearance, proteinuria, plasma glutathione peroxidase activity, urinary excretion of N-acetyl-β-d-glucosaminidase and histological analyses. Furthermore, DFO prevented the K(2)Cr(2)O(7)-induced renal oxidant stress and the decrease in the activity of the antioxidant enzymes superoxide dismutase, glutathione reductase, glutathione peroxidase, glutathione-S-transferase and catalase. Finally it was found that DFO, at 400mg/kg, decreases renal Cr(VI) content which prompted us to evaluate the potential Cr(VI) chelating properties of this compound. Indeed was found in an in vitro assay that DFO was an effective Cr(VI) chelator with an IC(50) of 800μg. In additional groups of rats was found that DFO posttreatment was ineffective to attenuate K(2)Cr(2)O(7)-induced nephrotoxicity and renal oxidant stress. Furthermore, DFO was unable to modify urinary excretion of total chromium. The nephroprotective effect of DFO against Cr(VI)-induced nephrotoxicity and oxidant stress may be explained, at least partially, by the ability of DFO to chelate Cr(VI) and to attenuate renal Cr(VI) content. However, it cannot be excluded that the ability of DFO to chelate iron may also be involved in the protection observed in our study. Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

  14. Determination of Chromium Valence Over the Range Cr(0)-Cr(VI) by Electron Energy Loss Spectroscopy

    Science.gov (United States)

    2006-01-01

    be of Cr (VI): Cr (V) [14,40-45] and Cr (IV) [46]. To fully altered by microbes [11-13], green algae [14], higher plants understand the geochemistry of Cr ... Cr (III) by bacteria [42,44,45] and Further, nearly all mineralized Cr in the terrestrial crust is green algae [14], reacts with diphenylcarbazide to...Determination of chromium valence over the range Cr (O)- Cr (VI) by electron energy loss spectroscopy Tyrone L. Daultona , Brenda J. Littleb ’Marine

  15. Cr(III) and Cr(VI) in leather and elicitation of eczema

    DEFF Research Database (Denmark)

    Hansen, Malene Barré; Menne, Torkil; Johansen, Jeanne Duus

    2006-01-01

    The aim of the present study was to investigate the relation between the content of Cr(VI) and soluble Cr(III) in leather and the ability of the leather to elicit eczema in chromium allergic patients. An array of chromium-tanned leather samples was analysed for the content of total Cr(VI) and sol......The aim of the present study was to investigate the relation between the content of Cr(VI) and soluble Cr(III) in leather and the ability of the leather to elicit eczema in chromium allergic patients. An array of chromium-tanned leather samples was analysed for the content of total Cr......(VI) and soluble Cr(III) using the DIN 53314 and the DS/EN 420 methods. Subsequently, a group of 15 patients with a history of foot eczema and leather exposure was exposed to a selection of 14 chromium- and 1 vegetable-tanned leather sample on the upper back for 48 hr. In addition, one leather sample was used...... not otherwise identified using an ordinary 48-hr exposure period. No relation was observed between the measured content of Cr(VI) and soluble Cr(III) in the leather and the elicitation of eczema. Thus, in order to evaluate the quality of chromium-tanned leather in relation to preventing allergic skin reactions...

  16. Effect of genotype, Cr(III and Cr(VI on plant growth and micronutrient status in Silene vulgaris (Moench

    Directory of Open Access Journals (Sweden)

    A. E. Pradas-del-Real

    2013-06-01

    Full Text Available Chromium released into the environment from industrial activities has become an important environmental concern. Silene vulgaris has been proven to be tolerant to many heavy metals, so it is considered an interesting species in the revegetation and restoration of polluted soils, but no information is available about its response to Cr. The objective of this work was to study uptake and influence on plant growth of Cr(III and Cr(VI in six genotypes (four hermaphrodites and two females of S. vulgaris from different sites of Madrid (Spain. Plants were treated for 12 days with 60 µM of Cr(III or Cr(VI in semihydroponics. Dry weights, soil-plant analysis development values (SPAD reading with chlorophylls and micronutrient and total Cr concentrations were determined. Metal uptake was higher in presence of Cr(VI than of Cr(III and poorly translocated to the shoots. In both cases S. vulgaris did not show visual toxicity symptoms, biomass reduction, or differences among SPAD values as consequence of Cr additions. However genotypes SV36 and SV38 showed Fe and Mn imbalance. This is the first report on the relatively good performance of hermaphrodite and female S. vulgaris genotypes in Cr uptake and physiological traits, but further studies will be necessary to elucidate the mechanisms by which the gender may influence these variables. S. vulgaris presented high diversity at genotypic level; the treatment with hexavalent Cr increased the differences among genotypes so the use of cuttings from an homogeneous genotype seems to be an adequate method for the study of this species.

  17. The effects of hydraulic retention time (HRT) on chromium(VI) reduction using autotrophic cultivation of Chlorella vulgaris.

    Science.gov (United States)

    Lee, Ling; Hsu, Chih-Yuan; Yen, Hong-Wei

    2017-12-01

    Chromium is an acutely toxic heavy metal that is known to be a carcinogen. Of the two predominant forms of chromium, Cr(III) and Cr(VI), Cr(III) has only about one thousandth the toxicity of Cr(VI). Using microalgal biomass is one way to remove Cr(VI) from the environment. Four days of hydraulic retention time (HRT) was required to completely reduce 10 mg/L of Cr(VI) in the influent. Microalgal biomass is conventionally regarded as an adsorbent in most Cr(VI) reduction studies. However, this study found that Chlorella vulgaris had the potential to convert Cr(VI) to Cr(III) through the enzymatic route of chromium reductase although the measured chromium reductase activity of C. vulgaris was less than that reported values obtained in bacteria. X-ray absorption near-edge spectroscopy (XANES) analysis further showed the absorption edge of Cr(III) in Cr(VI)-treated C. vulgaris, supporting the assumption of Cr(VI) potentially being converted to less-toxic Cr(III).

  18. USE OF MICRO X-RAY ABSORPTION SPECTROSCOPY AND DIFFRACTION TO DELINEATE Cr(VI) SPECIATION IN COPR

    Energy Technology Data Exchange (ETDEWEB)

    CHRYSOCHOOU, M.; MOON, D. H.; FAKRA, S.; MARCUS, M.; DERMATAS, D.; CHRISTODOULATOS, C.

    2010-06-22

    The speciation of Cr(VI) in Cromite Ore Processing Residue was investigated by means of bulk XRD, and a combination of micro-XRF, -XAS and -XRD at the Advanced Light Source (ALS), Berkeley, CA, U.S.A.. Bulk XRD yielded one group of phases that contained explicitly Cr(VI) in their structure, Calcium Aluminum Chromium Oxide Hydrates, accounting for 60% of the total Cr(VI). Micro-analyses at ALS yielded complimentary information, confirming that hydrogarnets and hydrotalcites, two mineral groups that can host Cr(VI) in their structure by substitution, were indeed Cr(VI) sinks. Chromatite (CaCrO4) was also identified by micro-XRD, which was not possible with bulk methods due to its low content. The acquisition of micro-XRF elemental maps enabled not only the identification of Cr(VI)-binding phases, but also the understanding of their location within the matrix. This information is invaluable when designing Cr(VI) treatment, to optimize release and availability for reduction.

  19. HMGA2 plays an important role in Cr (VI)-induced autophagy.

    Science.gov (United States)

    Yang, Fan; Zhao, Lian; Mei, Dan; Jiang, Liping; Geng, Chengyan; Li, Qiujuan; Yao, Xiaofeng; Liu, Yong; Kong, Ying; Cao, Jun

    2017-09-01

    Cr (VI) is mutagenic and carcinogenic, but the mechanism is unclear. In this study, the involvement of high mobility group A2 (HMGA2) in Cr (VI)-induced autophagy was investigated. Cr (VI) treatment induced formation of autophagosomes, increased expression of LC3II, Atg12-Atg5, Atg4, Atg10, HMGA1 and HMGA2 proteins, and decreased the expression of p62 in A549 cells. Silencing of HMGA2 gene by siRNA blocked Cr (VI)-induced formation of autophagosomes, expression of LC3II, Atg12-Atg5, Atg10 and reduction of p62. Overexpression of HMGA2 in HEK 293 and HeLa cells could induce the expression of LC3II, Atg12-Atg5 and Atg10, and decrease the expression of p62. Although the protein level of Atg12-Atg5 conjugation changed after Cr (VI) treatment, silencing of HMGA2 and overexpression of HMGA2, both the proteins and mRNA levels of Atg12 and Atg5 were not changed significantly. ChIP assay demonstrated that HMGA2 protein directly bound to the promoter sequence of Atg10 gene, which modulated the conjugation of Atg12-Atg5. Interestingly, 3-MA markedly prevented Cr (VI)-induced cell growth of A549 cells. Our further in vivo study confirmed that the expression of HMGA1, HMGA2, LC3II, Atg12-Atg5, Atg4, Atg5, Atg7, Atg10, Atg12, Beclin 1 were increased and p62 was reduced in lung tissues of Cr (VI)-treated BALB/c mice. Combining, our data demonstrated that HMGA2 plays an important role in Cr (VI)-induced autophagy and the mechanism underlies Atg12-Atg5 conjugation modulated by HMGA2-dependent transcriptional regulation of Atg10. This suggests that HMGA2 might be an important biomarker in Cr (VI)-induced autophagy, cell-growth or other toxicities. © 2017 UICC.

  20. Optimizing magnetic nanoparticles for drinking water technology: The case of Cr(VI)

    Energy Technology Data Exchange (ETDEWEB)

    Simeonidis, K., E-mail: ksime@physics.auth.gr [Department of Mechanical Engineering, School of Engineering, University of Thessaly, Volos 38334 (Greece); Kaprara, E. [Department of Chemical Engineering, Aristotle University of Thessaloniki, Thessaloniki 54124 (Greece); Samaras, T.; Angelakeris, M.; Pliatsikas, N.; Vourlias, G. [Department of Physics, Aristotle University of Thessaloniki, Thessaloniki 54124 (Greece); Mitrakas, M. [Department of Chemical Engineering, Aristotle University of Thessaloniki, Thessaloniki 54124 (Greece); Andritsos, N. [Department of Mechanical Engineering, School of Engineering, University of Thessaly, Volos 38334 (Greece)

    2015-12-01

    The potential of magnetite nanoparticles to be applied in drinking water treatment for the removal of hexavalent chromium is discussed. In this study, a method for their preparation which combines the use of low-cost iron sources (FeSO{sub 4} and Fe{sub 2}(SO{sub 4}){sub 3}) and a continuous flow mode, was developed. The produced magnetite nanoparticles with a size of around 20 nm, appeared relatively stable to passivation providing a removal capacity of 1.8 μg Cr(VI)/mg for a residual concentration of 50 μg/L when tested in natural water at pH 7. Such efficiency is explained by the reducing ability of magnetite which turns Cr(VI) to an insoluble Cr(OH){sub 3} form. The successful operation of a small-scale system consisting of a contact reactor and a magnetic separator demonstrates a way for the practical introduction and recovery of magnetite nanoparticles in water treatment technology. - Highlights: • Iron sulfates were used for the kilogram scale production of Fe{sub 3}O{sub 4} nanoparticles. • Studied particles showed a Cr(VI) removal capacity of 2 μg/mg in natural water. • Cr(VI) uptake is mostly based on its reduction and precipitation as Cr(OH){sub 3}. • A continuous flow reactor–magnetic separator operated with nanoparticles.

  1. Removal of Cr(VI) by surfactant modified Auricularia auricula spent substrate: biosorption condition and mechanism.

    Science.gov (United States)

    Dong, Liying; Jin, Yu; Song, Tao; Liang, Jinsong; Bai, Xin; Yu, Sumei; Teng, Chunying; Wang, Xin; Qu, Juanjuan; Huang, Xiaomei

    2017-07-01

    Auricularia auricula spent substrate (AASS) modified by didodecyldimethylammonium bromide(DDAB) was used as adsorbent to remove Cr(VI) from aqueous solution. Based on a single-factor experiment and response surface methodology, the optimal conditions were adsorbent dosage of 1.5 g/L, pH value of 4.0, initial Cr(VI) concentration of 19 mg/L, temperature of 25 °C, biosorption time of 120 min, rotational speed of 150 r/min, respectively, under which biosorption capacity could reach 12.16 mg/g compared with unmodified AASS (6.058 mg/g). DDAB modification could enlarge the specific surface area and porous diameter of the adsorbents, and supply hydrophilic and hydrophobic groups capable of adsorbing at the interfaces. In addition, DDAB increased ionic exchange and complex formation demonstrated by variations of elemental contents, shifts of carboxyl, amine groups, hydroxyl, alkyl chains, and phosphate groups as well as the crystal structure of the Cr-O compounds. Variations of peaks and energy in XPS analysis also testified the reduction of Cr(VI) to Cr(III).The biosorption behavior of modified AASS was in line with Langmuir and Freundlich isotherm equation. The final regeneration efficiency was 62.33% after three biosorption-desorption cycles. Apparently, DDBA is a eximious modifier and DDBA-modified AASS was very efficient for Cr(VI) removal.

  2. Facet-Dependent Cr(VI) Adsorption of Hematite Nanocrystals.

    Science.gov (United States)

    Huang, Xiaopeng; Hou, Xiaojing; Song, Fahui; Zhao, Jincai; Zhang, Lizhi

    2016-02-16

    In this study, the adsorption process of Cr(VI) on the hematite facets was systematically investigated with synchrotron-based Cr K-edge extended X-ray absorption fine structure (EXAFS) spectroscopy, in situ attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy, density-functional theory calculation, and surface complexation models. Structural model fitting of EXAFS spectroscopy suggested that the interatomic distances of Cr-Fe were, respectively, 3.61 Å for the chromate coordinated hematite nanoplates with exposed {001} facets, 3.60 and 3.30 Å for the chromate coordinated hematite nanorods with exposed {001} and {110} facets, which were characteristic of inner-sphere complexation. In situ ATR-FTIR spectroscopy analysis confirmed the presence of two inner-sphere surface complexes with C3ν and C2ν symmetry, while the C3ν and C2ν species were assigned to monodentate and bidentate inner-sphere surface complexes with average Cr-Fe interatomic distances of 3.60 and 3.30 Å, respectively. On the basis of these experimental and theoretical results, we concluded that HCrO4(-) as dominated Cr(VI) species was adsorbed on {001} and {110} facets in inner-sphere monodentate mononuclear and bidentate binuclear configurations, respectively. Moreover, the Cr(VI) adsorption performance of hematite facets was strongly dependent on the chromate complexes formed on the hematite facets.

  3. Polymer based nanocomposites for the removal of Cr(VI) from water

    CSIR Research Space (South Africa)

    Setshedi, K

    2012-10-10

    Full Text Available .3 pH 2 pH 6 % R em ov al pH Feasibility test for Cr(VI) contaminated ground water and the effect of competing ions 100 ppm Cr(VI) sol. Nanocomposite + Cr(VI) sol 0 ppm Cr(VI) sol. 0 20 40 60 80 100 Q e( m g/ g) Cr 6+ Cr 6... nanocomposites for the removal of Cr(VI) from water Emerging Researcher Symposium Katlego Setshedi 10 October 2012 Outline ? CSIR 2012 Slide 2 ? Background ? Problem statement ? Health impacts ? Remedies ? Objectives ? Experimental procedure...

  4. Isolation and characterization of Cr(VI)-reducing actinomycetes from estuarine sediments.

    Science.gov (United States)

    Terahara, Takeshi; Xu, Xudan; Kobayashi, Takeshi; Imada, Chiaki

    2015-04-01

    Bioremediation technologies have strong potential use in the less costly and more environmentally friendly removal of highly toxic hexavalent-chromium (Cr(VI)) compared with physicochemical technologies. Several Cr(VI)-reducing bacteria have been isolated; however, there are few studies on Cr(VI)-resistant and Cr(VI)-reducing actinomycetes. In this study, Cr(VI)-reducing actinomycetes were screened from estuarine, marine, and terrestrial samples on the basis of Cr(VI)-resistant and Cr(VI)-reducing ability. Of the 80 Streptomyces-like strains isolated, 20 strains were found to be resistant to 50 mg/l of Cr(VI). In addition, two strains isolated from the estuarine sediment of Tokyo Bay were found to be resistant to a concentration of 150 mg/l of Cr(VI). Furthermore, one Cr(VI)-reducing strain was found to remove 60 mg/l of Cr(VI) within 1 week and was identified as Streptomyces thermocarboxydus based on 16S rRNA gene analysis. The comparative evaluation with the type strain S. thermocarboxydus NBRC 16323 showed that our isolated strain had higher ability to grow at 27 °C and reduce Cr(VI) at a NaCl concentration of 6.0 % at 27 °C compared with the type strain NBRC 16323. These results indicate that our isolated strain have a potential ability to remove Cr(VI) from contaminated, highly saline sources without heating.

  5. Evaluation of Cr (VI) remediation potential of Eichornia sp in ...

    African Journals Online (AJOL)

    Purpose: Evaluation of Cr (VI) removal by indigenous chromium resistant bacterial strains alone and in combination with Eichornia sp. Methods: Three chromium resistant bacterial strains S-4 Ochrobactrum grignonense, SF-5 Bacillus sp. and S-6 Ochrobactrum pseudogrignonenses were isolated from industrial effluent.

  6. Characterization and application of the hetero-junction ZnFe2O4/TiO2 for Cr(VI) reduction under visible light

    National Research Council Canada - National Science Library

    G Rekhila; M Trari; Y Bessekhouad

    2017-01-01

    ...) into trivalent state. The transport properties, optical and photo-electrochemical characterizations are correlated, to build the energetic diagram of the hetero-system ZnFe2O4/TiO2/CrO4 - solution. A gap...

  7. Epithermal Neutron Activation Analysis (ENAA) of Cr(VI)-reducer Basalt-inhabiting Bacteria

    CERN Document Server

    Tsibakhashvili, N Ya; Kirkesali, E I; Aksenova, N G; Kalabegishvili, T L; Murusidze, I G; Mosulishvili, L M; Holman, H Y N

    2005-01-01

    Epithermal neutron activation analysis (ENAA) has been applied to studying elemental composition of Cr(VI)-reducer bacteria isolated from polluted basalts from the Republic of Georgia. Cr(VI)-reducing ability of the bacteria was examined by electron spin resonance (ESR) demonstrating that the bacteria differ in the rates of Cr(VI) reduction. A well-pronounced correlation between the ability of the bacteria to accumulate Cr(V) and their ability to reduce Cr(V) to Cr(III) observed in our experiments is discussed. Elemental analysis of these bacteria also revealed that basalt-inhabiting bacteria are distinguished by relative contents of essential elements such as K, Na, Mg, Fe, Mn, Zn, and Co. A high rate of Cr(III) formation correlates with a high concentration of Co in the bacterium. ENAA detected some similarity in the elemental composition of the bacteria. The relatively high contents of Fe detected in the bacteria (140-340 $\\mu $g/g of dry weight) indicate bacterial adaptation to the environmental condition...

  8. Physico-Chemical and Microbial Oxidation of Cr (III) to Cr (VI)

    African Journals Online (AJOL)

    Michael Horsfall

    ABSTRACT: The physico-chemical and microbial characteristics in soil was investigated in order to study the mobility and bioavailability ... surface level of the soil studied (conversion of Cr6+ in control soil was calculated as 0.15 mg kg-1 dry weight). Metal ..... or 10 mg Cr(VI) kg-1 soil reduced the respiration in soil. In axenic ...

  9. Cr(VI) formation during ozonation of Cr-containing materials in ...

    African Journals Online (AJOL)

    2011-10-14

    Oct 14, 2011 ... Ozonation, or advanced oxidation processes (utilising ozone decomposition products as oxidants) are widely used in industrial wastewater and .... iron particles can reduce Cr(VI) to Cr(III) in aqueous medium. Pulverising time was .... slightly heated water, which might be applicable to some industrial waste ...

  10. Reduction of chromium (VI) from aqueous solution by biomass of Cladosporium cladosporioides.

    Science.gov (United States)

    Garza-González, María Teresa; Ramírez-Vázquez, Jonathan Eduardo; García-Hernández, María de Los Ángeles; Cantú-Cárdenas, María Elena; Liñan-Montes, Adriana; Villarreal-Chiu, Juan Francisco

    2017-11-01

    The capacity of Cladosporium cladosporioides biomass for removal of Cr(VI) in aqueous solutions was evaluated. A 2 × 2 factorial experiment design was used to study the effects of pH and biomass doses. Lower pH values and larger biomass doses increased the capacity of C. cladosporioides biomass for removal of Cr(VI), reaching a reduction capacity of 492.85 mg g(-1), a significantly higher value compared to other biomass reported. Cr(VI) removal kinetic rates followed a pseudo-second order model, like other fungal biomass reported previously. The apparent adsorption process was described well by the Freundlich isothermal model. However, determination of total chromium indicated that adsorption of Cr(VI) was followed by a redox reaction that released proportional quantities of Cr(III) into the experimental supernatant, suggesting a parallel adsorption-reduction process. Comparison of Fourier transform infrared spectroscopy spectra of C. cladosporioides biomass before and after the reduction process demonstrated the involvement of positively charged amino groups in the Cr(VI) adsorption-reduction process.

  11. Enhanced Cr(VI) removal from groundwater by Fe0-H2O system with bio-amended iron corrosion.

    Science.gov (United States)

    Yin, Weizhao; Li, Yongtao; Wu, Jinhua; Chen, Guocai; Jiang, Gangbiao; Li, Ping; Gu, Jingjing; Liang, Hao; Liu, Chuansheng

    2017-06-15

    A one-pot bio-iron system was established to investigate synergetic abiotic and biotic effects between iron and microorganisms on Cr(VI) removal. More diverse iron corrosion and reactive solids, such as green rusts, lepidocrocite and magnetite were found in the bio-iron system than in the Fe 0 -H 2 O system, leading to 4.3 times higher Cr(VI) removal efficiency in the bio-iron system than in the Fe 0 -H 2 O system. The cycling experiment also showed that the Cr(VI) removal capacity of Fe 0 in the bio-iron system was 12.4 times higher than that in the Fe 0 -H 2 O system. A 62days of life-span could be achieved in the bio-iron system, while the Fe 0 -H 2 O system lost its efficacy after 30days. Enhanced effects of extra Fe 2+ on Cr(VI) removal was observed, largely contributed to the adsorbed Fe 2+ on iron surface, which could function as an extra reductant for Cr(VI) and promote the electron transfer on the solid phase. The results also showed that the reduction of Cr(VI) by microorganisms was insignificant, indicating the adsorption/co-precipitation of Cr by iron oxides on iron surface was responsible for the overall Cr(VI) removal. Our study demonstrated that the bio-amended iron corrosion could improve the performance of Fe 0 for Cr(VI) removal from groundwater. Copyright © 2017 Elsevier B.V. All rights reserved.

  12. Phytoremediation potential and nutrient status of Barringtonia acutangula Gaerth. Tree seedlings grown under different chromium (CrVI) treatments.

    Science.gov (United States)

    Kumar, Dharmendra; Tripathi, Durgesh Kumar; Chauhan, Devendra Kumar

    2014-02-01

    To investigate the effect of different chromium (CrVI) treatments on seedlings of semi-aquatic plant Barringtonia acutangula, hydroponic experiments were conducted. Results revealed that B. acutangula could tolerate much higher CrVI concentration accumulated about 751-2,703 mg kg(-1) dry weight in roots and 50-1,101 mg kg(-1) dry weight in shoots, respectively, under 1.0, 2.0, 3.0, 4.0, and 5.0 mM chromium treatments. CrVI exposure at 1.0-4.0 mM does not exhibit toxicity signs; however, up to 4.0 mM CrVI exposure causes significant decline in growth parameters. Content of macronutrients such as Ca and K decreased under different Cr treatments in roots and shoots, while Mg content of roots and shoots did not influence at the range of 1.0-4.0 mM Cr; however, significant decrease at 5.0 mM Cr, besides P content, significantly shows increasing trends, respectively. Interestingly, sulfur content of roots and shoots show increasing trends at 1.0-2.0 mM Cr; however, severe decrease of up to 3.0-5.0 mM is shown in CrVI treatments. Furthermore, micronutrients content were enhanced under CrVI treatments excluding Cu and Fe since they show significant reduction in shoots as well as in roots. Bioaccumulation factor were also calculated on the basis of results obtained which shows the value of >1 without viewing chromium toxicity symptoms. This study demonstrated that B. acutangula could tolerate CrVI concentrations up to 1.0-4.0 mM Cr which may be useful in chromium phytoremediation programs.

  13. Optimizing the application of magnetic nanoparticles in Cr(VI) removal

    Science.gov (United States)

    Simeonidis, Konstantinos; Kaprara, Efthymia; Mitrakas, Manassis; Tziomaki, Magdalini; Angelakeris, Mavroidis; Vourlias, Georgios; Andritsos, Nikolaos

    2013-04-01

    The presence of heavy metals in aqueous systems is an intense health and environmental problem as implied by their harmful effects on human and other life forms. Among them, chromium is considered as an acutely hazardous compound contaminating the surface water from industrial wastes or entering the groundwater, the major source of drinking water, by leaching of chromite rocks. Chromium occurs in two stable oxidation states, Cr(III) and Cr(VI), with the hexavalent form being much more soluble and mobile in water having the ability to enter easily into living tissues or cells and thus become more toxic. Despite the established risks from Cr(VI)-containing water consumption and the increasing number of incidents, the E.U. tolerance limit for total chromium in potable water still stands at 50 μg/L. However, in the last years a worldwide debate concerning the establishment of a separate and very strict limit for the hexavalent form takes place. In practice, Cr(VI) is usually removed from water by various methods such as chemical coagulation/filtration, ion exchange, reverse osmosis and adsorption. Adsorption is considered as the simplest method which may become very effective if the process is facilitated by the incorporation of a Cr(VI) to Cr(III) reduction stage. This work studies the potential of using magnetic nanoparticles as adsorbing agents for Cr(VI) removal at the concentration levels met in contaminated drinking water. A variety of nanoparticles consisting of ferrites MFe2O4 (M=Fe, Co, Ni, Cu, Mn, Mg, Zn) were prepared by precipitating the corresponding bivalent or trivalent sulfate salts under controlled acidity and temperature. Electron microscopy and X-ray diffraction techniques were used to verify their crystal structure and determine the morphological characteristics. The mean particle size of the samples was found in the range 10-50 nm. Batch Cr(VI) removal tests were performed in aqueous nanoparticles dispersions showing the efficiency of ferrite

  14. Synergy of photocatalysis and adsorption for simultaneous removal of Cr(VI) and Cr(III) with TiO₂ and titanate nanotubes.

    Science.gov (United States)

    Liu, Wen; Ni, Jinren; Yin, Xiaochen

    2014-04-15

    An one-step efficient simultaneous removal of Cr(VI) and Cr(III) was achieved with mixture of TiO₂ and titanate nanotubes (TNTs). Unlike the conventional two-step Cr removal with a first photocatalytic reduction of Cr(VI) and a subsequent adsorption of Cr(III), the proposed single process significantly reduced reaction time (over 50%). The synergy of photocatalysis and adsorption played an important role in enhancing Cr removal process. The synergetic mechanism was interpreted and indirectly confirmed with H₂O₂ variation during photocatalysis. The instant transfer of the reduced Cr from TiO₂ surface to TNTs interlayer greatly promoted the release of photocatalytic sites of TiO₂, which in turn considerably enhanced photocatalytic activity of TNTs by inhibiting electron-hole pairs recombination. The optimum condition for the whole process was at pH 5. Adsorption of Cr(III) was primarily in the interlayer of TNTs at pH ≤ 5. However, higher pH would lead to precipitation of Cr(OH)₃ onto TNTs as observed by X-ray photoelectron spectroscopy (XPS). Addition of Ca(2+) could promoted photocatalysis owing to its ionic bridging function and form of ≡TiOH(+)-Cr(VI)-Ca(2+)-Cr(VI) linkages, while SO₄(2-) only slightly inhibited photo-reduction of Cr(VI), indicating good synergy of photocatalysis and adsorption even at high ionic strength of electrolyte. Besides, the desorbed TNTs could be easily regenerated by remedying the damaged tubular structure and reused for Cr removal with excellent performance. The outstanding synergetic effects with essential explanation of the mechanism make this study not only fundamentally important but also potentially practical applicable. Copyright © 2014 Elsevier Ltd. All rights reserved.

  15. Single, simultaneous and consecutive biosorption of Cr(VI) and Orange II onto chemically modified masau stones.

    Science.gov (United States)

    Albadarin, Ahmad B; Solomon, Samuel; Kurniawan, Tonni Agustiono; Mangwandi, Chirangano; Walker, Gavin

    2017-12-15

    Novel and low cost chemically modified masau stone (CMMS) was investigated for its biosorption of an anionic azo dye, Orange II (OII), and toxic hexavalent chromium (Cr(VI)) from aqueous systems: individually, simultaneously and consecutively. XPS and FTIR analyses indicated the introduction of quaternary-Nitrogen to the CMMS surface after activation with epichlorohydrin (etherifying agent) and diethylenetriamine (crosslinking agent). The effects of pH, contact time and initial concentration (Co), and loading order on mechanisms of biosorption/reduction of OII and Cr(VI) onto CMMS were examined in detail. Several analytical techniques were employed to characterise the physio-chemical properties of the CMMS and determine the biosorption mechanisms. The pseudo second order and redox models were able to adequately predict the kinetics of biosorption. The Langmuir maximum OII biosorption capacity (qmax) was calculated as 136.8 mg/g for the dye onto the Cr(VI)-loaded CMMS consecutive system at Co = 100 mg/dm3. The qmax for the Cr(VI) system was found to be 87.32 mg/g at the same Co max. This reveals that the biosorption of OII and Cr(VI) mainly takes place via two different mechanisms i.e. hydrogen bonding and electrostatic attraction for the dye, and biosorption-coupled reduction for Cr(VI). Copyright © 2017 Elsevier Ltd. All rights reserved.

  16. Biosorption of Cr (VI) from aqueous solution by Rhizopus nigricans.

    Science.gov (United States)

    S Bai, R; Abraham, T E

    2001-08-01

    The study was aimed to quantify the Cr sorption ability of powdered biomass of Rhizopus nigricans at the best operating conditions. The influence of solution pH, agitation, Cr (VI) concentration, biomass dosage, contact time, biomass particle size and temperature were studied. The optimum pH for biosorption of Cr (VI) was found to be 2.0. Higher adsorption percentage was noted at lower initial concentrations of Cr ions, while the adsorption capacity of the biomass increased with increasing concentration of ions. Optimum biomass dosage was observed as 0.5% (w/v). More than 75% of the ions were removed within 30 min of contact and maximum removal was obtained after 8 h. Biomass particles of smaller size (90 microm) gave maximum adsorption (99.2%) at 100 mg/l concentration. The adsorption capacity increased with increase in temperature and agitation speed and the optimum were determined as 45 degrees C at 120 rpm. Freundlich and Langmuir isotherms were used to evaluate the data and the regression constants were derived. The adsorption rate constant values (Kad) were calculated for different initial concentration of Cr ions and the sorption was found to be higher at lower concentration (100 mg/l) of metal ion.

  17. Treatment of Cr(VI)-containing wastewaters with exopolysaccharide-producing cyanobacteria in pilot flow through and batch systems

    Energy Technology Data Exchange (ETDEWEB)

    Colica, Giovanni; Mecarozzi, Pier Cesare; De Philippis, Roberto [Florence Univ., Firenze (Italy). Dept. of Agricultural Biotechnology

    2010-08-15

    Seven exopolysaccharide-producing cyanobacteria were tested with regard to their capability to remove Cr(VI) from the wastewater of a plating industry. The cyanobacterium which showed, under lab conditions, the most promising features with regard to both Cr(VI) removal (about 12 mg of Cr(VI) removed per gram of dry biomass) and growth characteristics (highest growth rate and simplest culture medium) was Nostoc PCC7936. Furthermore, in lab experiments, it was also found that a HCl pretreatment is essential to abate the concentration of Cr(VI) in solution and that the viability of the biomass is not necessary. Subsequently, three pilot devices were tested, one batch (a dialysis cell) and two flow-through systems (a filter press and a column filled with quartz grain). The best performances were obtained with the filter press, where it was observed a sharp decrease in the concentration of Cr(VI), partly due to the adsorption of the metal by the biomass (about 50%) and partly due to its reduction to Cr(III). The results are discussed in terms of the role played by the different components (biomass and polysaccharide) of the cyanobacterial cultures in the removal of Cr(VI). (orig.)

  18. Nanosized amine-rich spheres embedded polymeric beads for Cr (VI) removal.

    Science.gov (United States)

    Lin, Peng; Liu, Chao; Li, Jiansheng; Qi, Junwen; Luo, Rui; Sun, Xiuyun; Shen, Jinyou; Han, Weiqing; Wang, Lianjun

    2017-12-15

    Porous matrix immobilization is considered as an effective approach to address the engineering challenges during practical application of nanoadsorbent. In this work, polyethersulfone (PES) beads with diameter of around 2.5mm, in which nanosized amine-rich polymer spheres (APSs) with particle size of ∼400nm are immobilized, are fabricated via phase inversion route. APSs-PES beads possess asymmetric and hierarchical structure with an exterior porous surface dense layer and numerous inner interpenetrating fingerlike channels, which promote the transportation of molecule and prevent the leaching of nanoadsorbents. The well distributed APSs with nitrogen-containing functional groups provide abundant adsorption sites. The cooperative attributing of the hierarchical structure and APSs demmonstrates enhanced Cr (VI) adsorption efficiency. The adsorption capacity of Cr (VI) is 243.9mg/g at 298K by Langmuir fitting. The effects of pH, temperature, the ratio of adsorbents and coexisting ionic are further studied in detail. The Cr (VI) removal mechanism is further explored by the combination of SEM, XPS, FTIR measurements and the adsorption parameters, further revealing the synergistic contribution of electrostatic attraction and reduction process. Therefore, this kind of adsorbents may show promising prospects on elimination of hazardous Cr (VI) in wastewater treatment. Copyright © 2017 Elsevier Inc. All rights reserved.

  19. EXTRACTION DU Cr(VI PAR MEMBRANE POLYMERE A INCLUSION

    Directory of Open Access Journals (Sweden)

    O KEBICHE SENHADJI

    2008-06-01

    Le pH de la solution aqueuse constituant la phase source est un paramètre clé dans l’opération de transport du Cr(VI à travers les MPIs étudiées. Un pH de 1,2 est recommandé pour la réalisation de l’extraction dans les conditions optimales déterminées.

  20. Total Reducing Capacity in Aquifer Minerals and Sediments: Quantifying the Potential to Attenuate Cr(VI) in Groundwater

    Energy Technology Data Exchange (ETDEWEB)

    Sisman, S. Lara [Univ. of Virginia, Charlottesville, VA (United States); Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2015-07-20

    Hexavalent chromium, Cr(VI), is present in the environment as a byproduct of industrial processes. Due to its mobility and toxicity, it is crucial to attenuate or remove Cr(VI) from the environment. The objective of this investigation was to quantify potential natural attenuation, or reduction capacity, of reactive minerals and aquifer sediments. Samples of reduced-iron containing minerals such as ilmenite, as well as Puye Formation sediments representing a contaminated aquifer in New Mexico, were reacted with chromate. The change in Cr(VI) during the reaction was used to calculate reduction capacity. This study found that minerals that contain reduced iron, such as ilmenite, have high reducing capacities. The data indicated that sample history may impact reduction capacity tests due to surface passivation. Further, this investigation identified areas for future research including: a) refining the relationships between iron content, magnetic susceptibility and reduction capacity, and b) long term kinetic testing using fresh aquifer sediments.

  1. Reduction and Removal of Chromium VI in Water by Powdered Activated Carbon

    Directory of Open Access Journals (Sweden)

    Yanan Chen

    2018-02-01

    Full Text Available Cr adsorption on wood-based powdered activated carbon (WPAC was characterized by scanning electron microscopy coupled with energy dispersive spectroscopy (SEM-EDS, Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS. The highest Cr(VI adsorption (40.04% was obtained under acidic conditions (pH 3, whereas Cr removal at pH 10 was only 0.34%. The mechanism of Cr(VI removal from aqueous solutions by WPAC was based on the reduction of Cr(VI to Cr(III with the concomitant oxidation of C-H and C-OH to C-OH and C=O, respectively, on the surface of WPAC, followed by Cr(III adsorption. Raman spectroscopy revealed a change in the WPAC structure in terms of the D/G band intensity ratio after Cr(VI adsorption. SEM-EDS analysis showed that the oxygen/carbon ratio on the WPAC surface increased from 9.85% to 17.74%. This result was confirmed by XPS measurements, which showed that 78.8% of Cr adsorbed on the WPAC surface was in the trivalent state. The amount of oxygen-containing functional groups on the surface increased due to the oxidation of graphitic carbons to C-OH and C=O groups.

  2. The role of iron chelators and oxygen in the reduced nicotinamide adenine dinucleotide phosphate-cytochrome P450 oxidoreductase-dependent chromium(VI) reduction.

    Science.gov (United States)

    Mikalsen, A; Capellmann, M; Alexander, J

    1995-03-01

    Chromium(VI) reduction was studied in a system composed of reduced nicotinamide adenine dinucleotide phosphate-cytochrome P450 oxidoreductase (NADPH-P450 reductase) and different iron chelators and iron sources. In an aerobic phosphate buffer containing iron(II), chromium(VI) was not reduced by the Fe2+ probably because of spontaneous autoxidation of Fe2+, but freshly made Fe2+, added directly to a CrVI-containing buffer, reduced CrVI. Under anaerobic conditions, iron(II) reduced chromium(VI) stoichiometrically. A systemic containing ethylenediaminetetraacetic acid (EDTA)-Fe3+, NADPH-P450 reductase and NADPH effectively reduced chromium(VI) anaerobically. Under aerobic conditions this reaction was inhibited by about 45%. Adenosine diphosphate (ADP)-Fe3+, which is a poor acceptor of electrons from NADPH-P450 reductase, reduced chromium(VI) only marginally, Mannitol slightly increased the aerobic CrVI reduction. Addition of superoxide dismutase and catalase, which both regenerate some O2, led to inhibition of CrVI reduction. Ferritin, NADPH-P450 reductase and the iron chelators, EDTA and citrate, reduced CrVI, indicating mobilization of Fe2+ from ferritin. Low levels of EDTA (55 mumol l-1) and citrate (100 mumol l-1) in contrast to high levels (5 mmol l-1) did not increase CrVI reduction in microsomes. Using 4-(2-hydroxyethyl)-1-piperazineethane sulfonic acid buffer instead of phosphate buffer, the CrVI-reducing activity was increased.

  3. Cr(VI) removal from wastewater using low cost sorbent materials: roots of Typha latifolia and ashes.

    Science.gov (United States)

    Barrera-Díaz, C; Colín-Cruz, A; Ureña-Nuñez, F; Romero-Romo, M; Palomar-Pardavé, M

    2004-08-01

    This work presents conditions for hexavalent chromium (Cr(VI)) removal from aqueous solution using different sorbent materials, namely: pyrolytic ashes of an industrial sludge from wastewater treatment and roots of Typha latifolia. The sorbent materials were characterized using scanning electron microscopy (SEM) and surface area using the Brunauer-Emmett-Teller (BET) technique, before and after the contact with the chromium-containing aqueous media. An overall Cr(VI) concentration reduction of 45% was achieved using the roots of Typha latifolia whereas in the case of pyrolytic ashes a 60% removal was observed. The percentage removal was found to depend on the initial Cr(VI) concentration in aqueous solution, pH and temperature. The Cr(VI) uptake process was maximum at pH 2 and a temperature of 40 degrees C for both sorbents. These materials showed a Cr(VI) adsorption capacity that was adequately described by the Langmuir adsorption isotherm. It was demonstrated that the use of waste materials for the treatment of Cr(VI)-containing wastewater is an effective and economical alternative method.

  4. Optimizing Cr(VI) and Tc(VII) remediation through nano-scale biomineral engineering

    Energy Technology Data Exchange (ETDEWEB)

    Cutting, R. S.; Coker, V. S.; Telling, N. D.; Kimber, R. L.; Pearce, C. I.; Ellis, B.; Lawson, R; van der Laan, G.; Pattrick, R.A.D.; Vaughan, D.J.; Arenholz, E.; Lloyd, J. R.

    2009-09-09

    To optimize the production of biomagnetite for the bioremediation of metal oxyanion contaminated waters, the reduction of aqueous Cr(VI) to Cr(III) by two biogenic magnetites and a synthetic magnetite was evaluated under batch and continuous flow conditions. Results indicate that nano-scale biogenic magnetite produced by incubating synthetic schwertmannite powder in cell suspensions of Geobacter sulfurreducens is more efficient at reducing Cr(VI) than either biogenic nano-magnetite produced from a suspension of ferrihydrite 'gel' or synthetic nano-scale Fe{sub 3}O{sub 4} powder. Although X-ray Photoelectron Spectroscopy (XPS) measurements obtained from post-exposure magnetite samples reveal that both Cr(III) and Cr(VI) are associated with nanoparticle surfaces, X-ray Magnetic Circular Dichroism (XMCD) studies indicate that some Cr(III) has replaced octahedrally coordinated Fe in the lattice of the magnetite. Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES) measurements of total aqueous Cr in the associated solution phase indicated that, although the majority of Cr(III) was incorporated within or adsorbed to the magnetite samples, a proportion ({approx}10-15 %) was released back into solution. Studies of Tc(VII) uptake by magnetites produced via the different synthesis routes also revealed significant differences between them as regards effectiveness for remediation. In addition, column studies using a {gamma}-camera to obtain real time images of a {sup 99m}Tc(VII) radiotracer were performed to visualize directly the relative performances of the magnetite sorbents against ultra-trace concentrations of metal oxyanion contaminants. Again, the magnetite produced from schwertmannite proved capable of retaining more ({approx}20%) {sup 99m}Tc(VII) than the magnetite produced from ferrihydrite, confirming that biomagnetite production for efficient environmental remediation can be fine-tuned through careful selection of the initial Fe(III) mineral

  5. Elucidating the mechanism of Cr(VI) formation upon the interaction with metal oxides during coal oxy-fuel combustion

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Juan [Department of Chemical Engineering, Monash University, Clayton, GPO Box 36, Victoria 3800 (Australia); State Key Laboratory of Coal Combustion, Huazhong University of Science and Technology, Wuhan 430074 (China); Jiao, Facun [Department of Applied Chemistry, Chubu University, 1200 Matsumoto-Cho, Kasugai, Aichi 487-8501 (Japan); Zhang, Lian, E-mail: lian.zhang@monash.edu [Department of Chemical Engineering, Monash University, Clayton, GPO Box 36, Victoria 3800 (Australia); Yao, Hong [State Key Laboratory of Coal Combustion, Huazhong University of Science and Technology, Wuhan 430074 (China); Ninomiya, Yoshihiko [Department of Applied Chemistry, Chubu University, 1200 Matsumoto-Cho, Kasugai, Aichi 487-8501 (Japan)

    2013-10-15

    Highlights: • The presence of Ca{sup 2+}/K{sup +} oxide in coal favored the enrichment of toxic Cr(VI) in coal combustion derived fly ash. • Fe{sub 2}O{sub 3} and MgO in coal are critical on the inhibition of Cr(VI) formation during coal combustion. • Cr(VI) formation extent is correlated positively with the standard reduction potential of metal oxide in coal. -- Abstract: The thermodynamics underpinning the interaction of Cr-bearing species with basic metal oxides, i.e. K{sub 2}O, Fe{sub 2}O{sub 3}, MgO and CaO, during the air and oxy-fuel combustion of coal have been examined. The synchrotron-based X-ray adsorption near-edge spectroscopy (XANES) was used for Cr speciation. For the oxides tested, Cr(VI) formation is dominated by the reduction potential of the metals. The oxides of Ca{sup 2+} with high reduction potential favored the oxidation of Cr(III), same for K{sup +}. The other two basic metals, Fe{sub 2}O{sub 3} and MgO with lower reduction potentials reacted with Cr(III) to form the corresponding chromites at the temperatures above 600 °C. Coal combustion experiments in drop-tube furnace have confirmed the rapid capture of Cr vapors, either trivalent or hexavalent, by CaO into solid ash. The existence of HCl in flue gas favored the vaporization of Cr as CrO{sub 2}Cl{sub 2}, which was in turn captured by CaO into chromate. Both Fe{sub 2}O{sub 3} and MgO exhibited less capability on scavenging the Cr(VI) vapor. Particularly, MgO alone exhibited a low capability for capturing the vaporized Cr(III) vapors. However, its co-existence with CaO in the furnace inhibited the Cr(VI) formation. This is beneficial for minimizing the toxicity of Cr in the coal combustion-derived fly ash.

  6. Simultaneous Reduction of Vanadium (V) and Chromium (VI) in Wastewater by Nanosized ZnWO4 Photocatalysis.

    Science.gov (United States)

    Zhao, Zengying; Zhang, Baogang; Chen, Daimei; Guo, Zhanhu; Peng, Zhijian

    2016-03-01

    Vanadium (V, V) and chromium (Cr, VI) are simultaneously photocatalytically reduced to less-toxic V(VI) and Cr(III) by mimetic solar light with ZnWO4 nanoparticles prepared by hydrothermal synthesis. The reduction efficiencies can reach 68.8% for V(V) and 97.3% for Cr(VI) in 3 h, respectively, which are comparable to those by microbial fuel cell technology carried out in over 10 days. The prepared ZnWO4 nanoparticles are characterized by XRD, SEM, EDS, TEM, and Uv-vis-DRS tests. Electrochemical calculation shows high acidity benefits the rapid reduction of V(V) and Cr(VI). In addition, the applied ZnWO4 nanoparticles can be recycled and reused for 5 repeated photocatalytic reduction runs. And after 5 runs, the recycled ZnWO4 nanoparticles can also present good photocatalytic activity with a reduction efficiency of about 60% for V(V) and 90% for Cr(VI). The new procedure on the simultaneous reduction of V(V) and Cr(VI) by photocatalysis may be promisingly applied in contaminated wastewaters, combining the remediation and possible V and Cr recovery.

  7. Adsorption of Cr(VI) onto Hybrid Membrane of Carboxymethyl Chitosan and Silicon Dioxide

    OpenAIRE

    Yanling Deng; Naoki Kano; Hiroshi Imaizumi

    2017-01-01

    In this study, a new adsorbent material was synthesized by using carboxymethyl chitosan and silicon dioxide. The hybrid membrane was used as an adsorbent for the removal of Cr(VI) from aqueous solutions. The adsorption potential of Cr(VI) by the hybrid materials was investigated by varying experimental conditions such as pH, contact time, and the dosage of the hybrid membrane. Adsorption isotherms of Cr(VI) onto the hybrid membrane were studied with varying initial concentrations under optimu...

  8. Remediation of chromium-slag leakage with electricity cogeneration via a urea-Cr(VI) cell

    OpenAIRE

    Binbin Yu; Huimin Zhang; Wei Xu; Gang Li; Zucheng Wu

    2014-01-01

    Chromium pollution has been historically widespread throughout the world. Most available remediation technologies often require energy consumption. This study is aimed to develop electrochemical remediation for Cr(VI) in chromium-slag leakage with self-generated electricity. Dynamic leaching experiments of chromium-slag samples were conducted to survey the release and leaching behavior of Cr(VI). Based on previous work, a unique urea-Cr(VI) was designed, in which urea was employed as the fuel...

  9. On the Stark broadening of Cr VI spectral lines in astrophysical plasma

    Science.gov (United States)

    Dimitrijević, M. S.; Simić, Z.; Sahal-Bréchot, S.

    2017-02-01

    Stark broadening parameters for Cr VI lines have been calculated using semiclassical perturbation method for conditions of interest for stellar plasma. Here are presented, as an example of obtained results, Stark broadening parameters for electron- and proton-impact broadening for Cr VI 4s 2S-4p 2P° λ = 1430 Å and Cr VI 4p 2P°-5s 2S λ = 611.8 Å multiplets. The obtained results are used to demonstrate the importance of Stark broadening of Cr VI in DO white dwarf atmospheres. Also the obtained results will enter in STARK-B database which is included in Virtual Atomic and Molecula Data Center - VAMDC.

  10. Cr(VI Adsorption on Red Mud Modified by Lanthanum: Performance, Kinetics and Mechanisms.

    Directory of Open Access Journals (Sweden)

    You-Wei Cui

    Full Text Available Water pollution caused by the highly toxic metal hexavalent chromium (Cr(VI creates significant human health and ecological risks. In this study, a novel adsorbent was used to treat Cr(VI-containing wastewater; the adsorbent was prepared using red mud (RM generated from the alumina production industry and the rare earth element lanthanum. This study explored adsorption performance, kinetics, and mechanisms. Results showed that the adsorption kinetics of the RM modified by lanthanum (La-RM, followed the pseudo-second-order model, with a rapid adsorption rate. Cr(VI adsorption was positively associated with the absorbent dose, pH, temperature, and initial Cr(VI concentration; coexisting anions had little impact. The maximum Cr(VI adsorption capacity was 17.35 mg/g. Cr(VI adsorption on La-RM was a mono-layer adsorption pattern, following the Langmuir isotherm model. Thermodynamic parameters showed the adsorption was spontaneous and endothermic. The adsorption of Cr(VI on La-RM occurred as a result of LaOCl formation on the RM surface, which in turn further reacted with Cr(VI in the wastewater. This study highlighted a method for converting industrial waste into a valuable material for wastewater treatment. The novel absorbent could be used as a potential adsorbent for treating Cr(VI-contaminating wastewater, due to its cost-effectiveness and high adsorption capability.

  11. Cr(VI) Adsorption on Red Mud Modified by Lanthanum: Performance, Kinetics and Mechanisms

    Science.gov (United States)

    Cui, You-Wei; Li, Jie; Du, Zhao-Fu; Peng, Yong-Zhen

    2016-01-01

    Water pollution caused by the highly toxic metal hexavalent chromium (Cr(VI)) creates significant human health and ecological risks. In this study, a novel adsorbent was used to treat Cr(VI)-containing wastewater; the adsorbent was prepared using red mud (RM) generated from the alumina production industry and the rare earth element lanthanum. This study explored adsorption performance, kinetics, and mechanisms. Results showed that the adsorption kinetics of the RM modified by lanthanum (La-RM), followed the pseudo-second-order model, with a rapid adsorption rate. Cr(VI) adsorption was positively associated with the absorbent dose, pH, temperature, and initial Cr(VI) concentration; coexisting anions had little impact. The maximum Cr(VI) adsorption capacity was 17.35 mg/g. Cr(VI) adsorption on La-RM was a mono-layer adsorption pattern, following the Langmuir isotherm model. Thermodynamic parameters showed the adsorption was spontaneous and endothermic. The adsorption of Cr(VI) on La-RM occurred as a result of LaOCl formation on the RM surface, which in turn further reacted with Cr(VI) in the wastewater. This study highlighted a method for converting industrial waste into a valuable material for wastewater treatment. The novel absorbent could be used as a potential adsorbent for treating Cr(VI)-contaminating wastewater, due to its cost-effectiveness and high adsorption capability. PMID:27658113

  12. Cr (VI) induced oxidative stress and toxicity in cultured cerebellar granule neurons at different stages of development and protective effect of Rosmarinic acid.

    Science.gov (United States)

    Dashti, Abolfazl; Soodi, Maliheh; Amani, Nahid

    2016-03-01

    Chromium (Cr) is a widespread metal ion in the workplace, industrial effluent, and water. The toxicity of chromium (VI) on various organs including the liver, kidneys, and lung were studied, but little is known about neurotoxicity. In this study, neurotoxic effects of Cr (VI) have been investigated by cultured cerebellar granule neurons (CGNs). Immature and mature neurons were exposed to different concentrations of potassium dichromate for 24 h and cytotoxicity was measured by MTT assay. In addition, immature neurons were exposed for 5 days as regards cytotoxic effect in development stages. The reactive oxygen species (ROS), mitochondrial membrane potential (MMP) and the protective effect of Rosmarinic acid on mature and immature neurons exposed to potassium dichromate, were measured. Furthermore, lipid peroxidation, glutathione peroxidase (GPx), and acetylcholinesterase activity in mature neurons were assessed following exposure to potassium dichromate. The results indicate that toxicity of Cr (VI) dependent on maturation steps. Cr (VI) was less toxic for immature neurons. Also, Cr (VI) induced MMP reduction and ROS production in both immature and mature neurons. In Cr (VI) treated neurons, increased lipid peroxidation and GPx activity but not acetylcholinesterase activity was observed. Interestingly, Rosmarinic acid, as a natural antioxidant, could protect mature but not immature neurons against Cr (VI) induced toxicity. Our findings revealed vulnerability of mature neurons to Cr (VI) induced toxicity and oxidative stress. © 2014 Wiley Periodicals, Inc.

  13. Simultaneous microbial reduction of vanadium (V) and chromium (VI) by Shewanella loihica PV-4.

    Science.gov (United States)

    Wang, Guangyu; Zhang, Baogang; Li, Shuang; Yang, Meng; Yin, Changcheng

    2017-03-01

    Toxic vanadium (V) and chromium (VI) often co-exist in wastewater from vanadium ore smelting and their reductions by bacterial strain Shewanella loihica PV-4 is realized simultaneously. After 27-d operation, 71.3% of V(V) and 91.2% of Cr(VI) were removed respectively, with citrate as organic carbon source. Enhancement of Cr(VI) bioreduction was observed with the suppressed V(V) reduction. V(IV) and Cr(III), the main reduction products, precipitated inside the organisms and attached on cell surfaces. Both membrane components containing cytochrome c and cytoplasmic fractions containing soluble proteins as well as NADH may contribute to these microbial reductions. Most Cr(VI) were reduced extracellularly and V(V) tended to be reduced through intracellular process, as revealed by mapping the microbial surface and a line scan across the cell, performed by scanning transmission electron microscopy. This study provides an efficient alternative for controlling combined pollution caused by these two metals based on microbial technology. Copyright © 2016 Elsevier Ltd. All rights reserved.

  14. Study of the involved sorption mechanisms of Cr(VI) and Cr(III) species onto dried Salvinia auriculata biomass.

    Science.gov (United States)

    Módenes, Aparecido Nivaldo; de Oliveira, Ana Paula; Espinoza-Quiñones, Fernando R; Trigueros, Daniela Estelita Goes; Kroumov, Alexander Dimitrov; Bergamasco, Rosângela

    2017-04-01

    Removal of Cr(VI) species by dried biomass of the aquatic macrophyte Salvinia auriculata was studied in order to understand the involved sorption mechanisms. Kinetic tests were carried out under the conditions such as concentration range of Cr(VI) from 50 to 250 mg L-1 and a temperature of 30 °C. Modification of the biosorbent by the presence of Cr(VI) species was assessed by analysis of its porosity, density and infrared molecular absorption spectrum. A series of experimental approaches involving directed chemical modifications on the biosorbent surface was performed. The main functional groups involved in the sorption mechanisms were identified. The gas sorption analyser was applied and proved that a strong chemical effect of Cr(VI) species on the surface took place, resulting in a leaching organic matter with an obvious and significant increase in the porosity parameters. The intra-particle diffusion model revealed different mass transfer zones into the adsorbent during Cr(VI) removal. New combined Langmuir and Dubinin-Radushkevich isotherm was the best to fit the equilibrium data of Cr(VI) species removal. Finally, Cr(VI) removal was mainly mediated by a redox process where Cr(III) species were formed. Copyright © 2017 Elsevier Ltd. All rights reserved.

  15. On the passivation mechanism of Fe{sub 3}O{sub 4} nanoparticles during Cr(VI) removal from water: A XAFS study

    Energy Technology Data Exchange (ETDEWEB)

    Pinakidou, F., E-mail: fpina@physics.auth.gr [Aristotle University of Thessaloniki, Department of Chemical Engineering, Analytical Chemistry Laboratory, 54124 Thessaloniki (Greece); Katsikini, M. [Aristotle University of Thessaloniki, School of Physics, Section of Solid State Physics, 54124 Thessaloniki (Greece); Simeonidis, K.; Kaprara, E. [Aristotle University of Thessaloniki, Department of Chemical Engineering, Analytical Chemistry Laboratory, 54124 Thessaloniki (Greece); Paloura, E.C. [Aristotle University of Thessaloniki, School of Physics, Section of Solid State Physics, 54124 Thessaloniki (Greece); Mitrakas, M. [Aristotle University of Thessaloniki, Department of Chemical Engineering, Analytical Chemistry Laboratory, 54124 Thessaloniki (Greece)

    2016-01-01

    Graphical abstract: - Highlights: • Presence of Fe(II) even after high Cr-loading. • The vacancies in the γ-Fe{sub 2}O{sub 3} layer formed offer sites for Cr(III) sorption. • Cr(III) sorbs into the vacancies and Cr(VI) forms outer sphere complexes. • Increasing surface Cr(III) loading changes the polymerization of the Fe–O–Fe chains. • Cr(III) sorption modifies Fe{sub 3}O{sub 4} structure obstructing further Cr(VI) removal. - Abstract: X-Ray Absorption Spectroscopies (XAFS) are employed in order to gather a thorough insight on the uptake mechanism of Cr(VI) by Fe{sub 3}O{sub 4} nanoparticles under water treatment conditions. The XANES measurements identify that the reducing potential of Fe{sub 3}O{sub 4} activates the precipitation of Cr(VI) in the form of insoluble and non-toxic Cr(III). However, electron donation from Fe(II) is responsible for its gradual consumption, resulting in the presence of a surface maghemite layer and the formation of structural vacancies. EXAFS analysis reveal that adsorption of Cr(III)-oxyanions occurs on sorption sites provided by the vacancies in the maghemite layer, where Cr(III) is involved in a bidentate binuclear ({sup 2}E) geometry with Fe-octahedra while it also forms monodentate ({sup 1}V) complexes with the Fe(III)O{sub 4} tetrahedra. The surface maghemitization along with the reduced Cr(III) adsorption into the vacancies, tracks the degree of Cr-reduction, since this surface structural modifications hinder Cr(VI) access to the Fe(II) ions of the magnetite nanoparticles. Thus, high surface coverage leads to the passivation of the reduction ability since physisorbed Cr(VI) is also detected through the formation of outer sphere complexes.

  16. Enhanced Cr(VI) removal from groundwater by Fe0-H2O system with bio-amended iron corrosion

    DEFF Research Database (Denmark)

    Yin, Weizhao; Li, Yongtao; Wu, Jinhua

    2017-01-01

    Abstract A one-pot bio-iron system was established to investigate synergetic abiotic and biotic effects between iron and microorganisms on Cr(VI) removal. More diverse iron corrosion and reactive solids, such as green rusts, lepidocrocite and magnetite were found in the bio-iron system than...... in the Fe0-H2O system, leading to 4.3 times higher Cr(VI) removal efficiency in the bio-iron system than in the Fe0-H2O system. The cycling experiment also showed that the Cr(VI) removal capacity of Fe0 in the bio-iron system was 12.4 times higher than that in the Fe0-H2O system. A 62 days of life......-span could be achieved in the bio-iron system, while the Fe0-H2O system lost its efficacy after 30 days. Enhanced effects of extra Fe2+ on Cr(VI) removal was observed, largely contributed to the adsorbed Fe2+ on iron surface, which could function as an extra reductant for Cr(VI) and promote the electron...

  17. Adsorption of Cr(VI) and speciation of Cr(VI) and Cr(III) in aqueous solutions using chemically modified chitosan.

    Science.gov (United States)

    Dai, Jun; Ren, FengLian; Tao, ChunYuan

    2012-05-01

    A new type of grafting chitosan (CTS) was synthesized using 2-hydroxyethyl-trimethyl ammonium chloride (HGCTS). The adsorption of Cr(VI) on HGCTS was studied. The effect factors on adsorption and the adsorption mechanism were considered. The results indicated that the HGCTS could concentrate and separate Cr(VI) at pH 4.0; the adsorption equilibrium time was 80 min; the maximum adsorption capacity was 205 mg/g. The adsorption isotherm and kinetics were investigated, equilibrium data agreed very well with the Langmuir model and the pseudo second-order model could describe the adsorption process better than the pseudo first-order model. A novel method for speciation of Cr(VI) and Cr(III) in environmental water samples has been developed using HGCTS as adsorbent and FAAS as determination means. The detection limit of this method was 20 ng/L, the relatively standard deviation was 1.2% and the recovery was 99%~105%.

  18. Adsorption of Cr(VI and Speciation of Cr(VI and Cr(III in Aqueous Solutions Using Chemically Modified Chitosan

    Directory of Open Access Journals (Sweden)

    ChunYuan Tao

    2012-05-01

    Full Text Available A new type of grafting chitosan (CTS was synthesized using 2-hydroxyethyl- trimethyl ammonium chloride (HGCTS. The adsorption of Cr(VI on HGCTS was studied. The effect factors on adsorption and the adsorption mechanism were considered. The results indicated that the HGCTS could concentrate and separate Cr(VI at pH 4.0; the adsorption equilibrium time was 80 min; the maximum adsorption capacity was 205 mg/g. The adsorption isotherm and kinetics were investigated, equilibrium data agreed very well with the Langmuir model and the pseudo second-order model could describe the adsorption process better than the pseudo first-order model. A novel method for speciation of Cr(VI and Cr(III in environmental water samples has been developed using HGCTS as adsorbent and FAAS as determination means. The detection limit of this method was 20 ng/L, the relatively standard deviation was 1.2% and the recovery was 99%~105%.

  19. Enhanced biotic and abiotic transformation of Cr(vi) by quinone-reducing bacteria/dissolved organic matter/Fe(iii) in anaerobic environment.

    Science.gov (United States)

    Huang, Bin; Gu, Lipeng; He, Huan; Xu, Zhixiang; Pan, Xuejun

    2016-09-14

    This study investigated the simultaneous transformation of Cr(vi) via a closely coupled biotic and abiotic pathway in an anaerobic system of quinone-reducing bacteria/dissolved organic matters (DOM)/Fe(iii). Batch studies were conducted with quinone-reducing bacteria to assess the influences of sodium formate (NaFc), electron shuttling compounds (DOM) and the Fe(iii) on Cr(vi) reduction rates as these chemical species are likely to be present in the environment during in situ bioremediation. Results indicated that the concentration of sodium formate and anthraquinone-2-sodium sulfonate (AQS) had apparently an effect on Cr(vi) reduction. The fastest decrease in rate for incubation supplemented with 5 mM sodium formate and 0.8 mM AQS showed that Fe(iii)/DOM significantly promoted the reduction of Cr(vi). Presumably due to the presence of more easily utilizable sodium formate, DOM and Fe(iii) have indirect Cr(vi) reduction capability. The coexisting cycles of Fe(ii)/Fe(iii) and DOM(ox)/DOM(red) exhibited a higher redox function than the individual cycle, and their abiotic coupling action can significantly enhance Cr(vi) reduction by quinone-reducing bacteria.

  20. An automatic micro-sequential injection bead injection lab-on-valve (muSI-BI-LOV) assembly for speciation analysis of ultra trace levels of Cr(III) and Cr(VI) incorporating on-line chemical reduction and employing detection by electrothermal atomic absorption spectrometry (ETAAS)

    DEFF Research Database (Denmark)

    Long, Xiangbao; Miró, Manuel; Hansen, Elo Harald

    2005-01-01

    and preconcentrated on the beads and subsequently eluted by a small volume of eluent (0.1 mol L-1 HNO3) and quantified by ETAAS, the Cr(VI) ions in the second portion are mixed with a reducing agent and parked under stopped-flow conditions in an open tubular reactor attached to one of the peripheral ports of the LOV...

  1. A survey of Cr(VI) contamination of surface water in the proximity of ...

    African Journals Online (AJOL)

    In this study, Cr(VI) levels present in surface water within the vicinity of ferrochrome smelters located in the Bushveld Igneous Complex were monitored for a period of 1 year. The results indicated that surface water in the proximity of ferrochrome smelters was mostly unaffected by Cr(VI) pollution. Two surface water sampling ...

  2. and Cr(VI) ions by chitosan: kinetics and equilibrium studies

    African Journals Online (AJOL)

    The ability of chitosan as an adsorbent for Cu (II) and Cr (VI) ions in aqueous solution was studied. The experiments were done as batch processes. Equilibrium studies were done on both cross-linked and non-cross-linked chitosan for both metals. Cr (VI) adsorption behaviour could be described using the Langmuir ...

  3. Optimum pHs for Cr(VI) co-removal with nucleated Cu(II ...

    African Journals Online (AJOL)

    A compact nucleated precipitation technology using two fluidised sand columns in series was developed to pretreat model metal-plating wastewater containing high concentrations of Cu(II) and Cr(VI). Since either Cu(II) precipitation or Cr(VI) co-removal with Cu(II) precipitation was found to be highly pH dependent in batch ...

  4. Modelling Cr(VI) removal by a combined carbon-activated sludge system

    Energy Technology Data Exchange (ETDEWEB)

    Orozco, A. Micaela Ferro [Centro de Investigacion y Desarrollo en Criotecnologia de Alimentos (CIDCA), CONICET, Fac. de Cs. Exactas, UNLP. 47 y 116 (B1900AJJ), La Plata (Argentina); Contreras, Edgardo M. [Centro de Investigacion y Desarrollo en Criotecnologia de Alimentos (CIDCA), CONICET, Fac. de Cs. Exactas, UNLP. 47 y 116 (B1900AJJ), La Plata (Argentina)], E-mail: econtrer@quimica.unlp.edu.ar; Zaritzky, Noemi E. [Centro de Investigacion y Desarrollo en Criotecnologia de Alimentos (CIDCA), CONICET, Fac. de Cs. Exactas, UNLP. 47 y 116 (B1900AJJ), La Plata (Argentina); Fac. de Ingenieria, UNLP. 47 y 1 (B1900AJJ), La Plata (Argentina)

    2008-01-15

    The combined carbon-activated sludge process has been proposed as an alternative to protect the biomass against toxic substances in wastewaters; however, the information about the effect of powdered-activated carbon (PAC) addition in activated sludge reactors for the treatment of wastewaters containing Cr(VI) is limited. The objectives of the present study were: (a) to evaluate the removal of hexavalent chromium by (i) activated sludge microorganisms in aerobic batch reactors, (ii) powdered-activated carbon, and (iii) the combined action of powdered-activated carbon and biomass; (b) to propose mathematical models that interpret the experimental results. Different Cr(VI) removal systems were tested: (S1) biomass (activated sludge), (S2) PAC, and (S3) the combined activated carbon-biomass system. A Monod-based mathematical model was used to describe the kinetics of Cr(VI) removal in the system S1. A first-order kinetics with respect to Cr(VI) and PAC respectively, was proposed to model the removal of Cr(VI) in the system S2. Cr(VI) removal in the combined carbon-biomass system (S3) was faster than both Cr(VI) removal using PAC or activated sludge individually. Results showed that the removal of Cr(VI) using the activated carbon-biomass system (S3) was adequately described by combining the kinetic equations proposed for the systems S1 and S2.

  5. Three-Dimensional Zn0.5Cd0.5S/Reduced Graphene Oxide Hybrid Aerogel: Facile Synthesis and the Visible-Light-Driven Photocatalytic Property for Reduction of Cr(VI in Water

    Directory of Open Access Journals (Sweden)

    Wei Xiao

    2016-01-01

    Full Text Available A series of three-dimensional ZnxCd1-xS/reduced graphene oxide (ZnxCd1-xS/RGO hybrid aerogels was successfully synthesized based on a one-pot hydrothermal approach, which were subsequently used as visible-light-driven photocatalysts for photoreduction of Cr(VI in water. Over 95% of Cr(VI was photoreduced by Zn0.5Cd0.5S/RGO aerogel material within 140 min, and such photocatalytic performance was superior to that of other ZnxCd1-xS/RGO aerogel materials (x≠0.5 and bare Zn0.5Cd0.5S. It was assumed that the enhanced photocatalytic activity of Zn0.5Cd0.5S/RGO aerogel was attributed to its high specific surface area and the preferable synergetic catalytic effect between Zn0.5Cd0.5S and RGO. Besides, Zn0.5Cd0.5S/RGO aerogel materials were robust and durable enough so that they could be reused several times with merely limited loss of photocatalytic activity. The chemical composition, phase, structure, and morphology of Zn0.5Cd0.5S/RGO aerogel material were carefully examined by a number of techniques like XRD, SEM, TEM, BET, Raman characterizations, and so on. It was found that Zn0.5Cd0.5S/RGO aerogel possessed hierarchically porous architecture with the specific surface area as high as 260.8 m2 g−1. The Zn0.5Cd0.5S component incorporated in Zn0.5Cd0.5S/RGO aerogel existed in the form of solid solution nanoparticles, which were uniformly distributed in the RGO matrix.

  6. Selective adsorption of Cr(VI) ions from aqueous solutions using Cr(6+)-imprinted Pebax/chitosan/GO/APTES nanofibrous adsorbent.

    Science.gov (United States)

    Etemadi, Mohammadmahdi; Samadi, Saman; Yazd, Shabnam Sharif; Jafari, Pooya; Yousefi, Negin; Aliabadi, Majid

    2017-02-01

    In the present study, a novel Cr(6+)-imprinted Pebax/chitosan/GO/APTES nanofibrous adsorbent (Cr(6+)-PCGA) was prepared and its performance was compared with PCGA nanofibers for selective sorption of Cr(VI) ions from aqueous solutions. The prepared nanofibers were characterized using FTIR, SEM and EDAX analysis. The influence of batch sorption experiments including GO/APTES content, pH, contact time, Cr(VI) initial concentration and temperature on the Cr(VI) sorption efficiency using synthesized nanofibers was investigated. The Cr(VI) sorption data were well described using pseudo-second-order kinetic and Redlich-Peterson isotherm models. The maximum sorption capacities of Cr(6+)-PCGA and PCGA nanofibers for Cr(VI) ions sorption were found to be 204.5 and 550.5mgg(-1), respectively. Thermodynamic studies indicated an endothermic and spontaneous nature of Cr(VI) ions sorption using both Cr(6+)-PCGA and PCGA nanofibers. The selectivity coefficient values of Cr(VI)/Pb(II), Cr(VI)/Cu(II) and Cr(VI)/Ni(II) indicated the higher selectivity of Cr(6+)-PCGA nanofibrous adsorbent for Cr(VI) ions separation compared to PCGA nanofibers. The good stability and reusability of Cr(6+)-PCGA nanofibrous adsorbent for five sorption/desorption cycles promised a higher potential of ion-imprinted nanofibers for separation of metal ions from aqueous systems in a large scale. Copyright © 2016 Elsevier B.V. All rights reserved.

  7. Hexavalent Chromium (Cr(VI Down-Regulates Acetylation of Histone H4 at Lysine 16 through Induction of Stressor Protein Nupr1.

    Directory of Open Access Journals (Sweden)

    Danqi Chen

    Full Text Available The environmental and occupational carcinogen Hexavalent Chromium (Cr(VI has been shown to cause lung cancer in humans when inhaled. In spite of a considerable research effort, the mechanisms of Cr(VI-induced carcinogenesis remain largely unknown. Nupr1 (nuclear protein 1 is a small, highly basic, and unfolded protein with molecular weight of 8,800 daltons and is induced by a variety of stressors. Studies in animal models have suggested that Nupr1 is a key factor in the development of lung and pancreatic cancers, with little known about the underlying molecular mechanisms. Here we report that the level of Nupr1 is significantly increased in human bronchial epithelial BEAS2B cells following exposure to Cr(VI through epigenetic mechanisms. Interestingly, Cr(VI exposure also results in the loss of acetylation at histone H4K16, which is considered a 'hallmark' of human cancer. Cr(VI-induced reduction of H4K16 acetylation appears to be caused by the induction of Nupr1, since (a overexpression of Nupr1 decreased the levels of both H4K16 acetylation and the histone acetyltransferase MOF (male absent on the first; also known as Kat8, Myst 1, which specifically acetylates H4K16; (b the loss of acetylation of H4K16 upon Cr(VI exposure is greatly compromised by knockdown of Nupr1. Moreover, Nupr1-induced reduction of H4K16 acetylation correlates with the transcriptional down-regulation at several genomic loci. Notably, overexpression of Nupr1 induces anchorage-independent cell growth and knockdown of Nupr1 expression prevents Cr(VI-induced cell transformation. We propose that Cr(VI induces Nupr1 and rapidly perturbs gene expression by downregulating H4K16 acetylation, thereby contributing to Cr(VI-induced carcinogenesis.

  8. Radiation induced environmental remediation of Cr(VI) heavy metal in aerated neutral solution under simulated industrial effluent

    Energy Technology Data Exchange (ETDEWEB)

    Djouider, Fathi; Aljohani, Mohammed S. [King Abdulaziz Univ., Jeddah (Saudi Arabia). Nuclear Engineering Dept.

    2017-08-01

    Cr(VI) compounds are major water contaminants in most industrial effluents, due to their carcinogenicity, while Cr(III) is an important element for human metabolism. In a previous work, we showed that Cr(VI) was radiolytically reduced to Cr(III) by the CO{sub 2}{sup -.} radical at pH 3 N{sub 2}O-saturated solution in the presence of formate. Here in the present work, this removal was investigated by steady state irradiation and pulse radiolysis in aerated solution at neutral pH, which is close to natural conditions in most wastewaters, where the reducing agent is the superoxide radical anion O{sub 2}{sup -.} The degradation of Cr(VI) increased linearly with the absorbed dose and was significantly enhanced by the added formate but not by the radiolitically produced hydrogen peroxide at this pH. The rate constant for this reduction was found to be 1.28 x 10{sup 8} M{sup -1} s{sup -1} and the absorption spectrum of Cr(V) transient species was obtained. A partial recovery of Cr(VI) is observed over a period of ca. 5 ms following a second order kinetics with a rate constant 8.0 x 10{sup 6} M{sup -1} s{sup -1}. These outcomes suggest that gamma-irradiation of Cr(VI)-contaminated wastewaters and industrial effluents in presence of formate can be simple, effective and economical means for the remediation of this major contaminant.

  9. Tolerance and Reduction of Chromium(VI by Bacillus sp. MNU16 Isolated from Contaminated Coal Mining Soil

    Directory of Open Access Journals (Sweden)

    Neha Upadhyay

    2017-05-01

    Full Text Available The bacterium MNU16 was isolated from contaminated soils of coal mine and subsequently screened for different plant growth promoting (PGP activities. The isolate was further identified by 16S rRNA sequencing as Bacillus subtilis MNU16 with IAA concentration (56.95 ± 0.43 6μg/ml, siderophore unit (9.73 ± 2.05%, phosphate solubilization (285.13 ± 1.05 μg/ml and ACC deaminase activity (116.79 ± 0.019 μmoles α-ketobutyrate/mg/24 h. Further, to evaluate the metal resistance profile of bacterium, the isolate was screened for multi-metal resistance (viz. 900 mg/L for Cr, 600 mg/L for As, 700 mg/L for Ni and 300 mg/L for Hg. Additionally, the resistance pattern of B. subtilis MNU16 against Cr(VI (from 50 to 300 mg/L treatments were evaluated. An enriched population was observed at 0–200 mg/L Cr(VI concentration while slight reductions were observed at 250 and 300 mg/L Cr(VI. Further, the chromium reduction ability at 50 mg/L of Cr(VI highlighted that the bacterium B. subtilis MNU16 reduced 75% of Cr(VI to 13.23 mg/L within 72 h. The localization of electron dense precipitates was observed in the TEM images of B. subtilis MNU16 which is might be due to the reduction of Cr(VI to Cr(III. The data of fluorescence microscopy and flow cytometry with respect to Cr(VI treatments (50–300 mg/L showed a similar pattern and clearly revealed the less toxic effect of hexavalent chromium upto 200 mg/L Cr(VI concentration. However, toxicity effects were more pronounced at 300 mg/L Cr(VI. Therefore, the present study suggests that the plant growth promoting potential and resistance efficacy of B. subtilis MNU16 will go a long way in developing an effective bioremediation approach for Cr(VI contaminated soils.

  10. [Simultaneous remediation of Cr (VI) and p-NCB by nanosacle iron].

    Science.gov (United States)

    Niu, Shao-feng; Li, Chun-hui; Lou, Zhang-hua; Xu, Yue-ping

    2009-01-01

    Nanoscale Fe and Ni/Fe, which were prepared by chemical deposition, were utilized as catalyst for remediation of Cr(VI) and pNCB in contaminated water. The interactions between Cr( VI) and p-NCB in contaminated water during the simultaneous remediation process were analyzed. It is demonstrated from the experiment that p-NCB can be degradated into p-CAN by nanoscale iron, but cannot exhibit the effect of dechlorination, and that there is a competitive relationship between Cr( VI) and p-NCB in the remediation process. The nanoscale Nil Fe bimetals could be applied in simultaneous remediation of p-NCB with Cr( VI) and give rise to a good remediation efficiency, where the products are only Cr(III) and p-CAN without any intermediate products. It was found that the conditions of higher Ni(II) concentration can promote the degradation rate of p-NCB. The optimum Ni/Fe ratio is 1:50. Whereas, the higher concentrations of Cr(VI) and p-NCB will lead to the lower degradation rate. Under the condition that concentration of Cr (VI) was 20 mg/L, the corresponding maximum dechlorination of p-NCB was 43.0%; under the condition that concentration of p-NCB was 40 mg/L, the corresponding maximum removal efficiency of Cr(VI) was 71.4%.

  11. Biosorption of Cr(III), Cr(VI), Cu(II) ions by intact cells of Spirulina platensis

    OpenAIRE

    Gelagutashvili, E.; Bagdavadze, N.; Rcheulishvili, A.

    2017-01-01

    The absorption characteristics of Cr(III), Cr(VI), Cu(II) ions on intact living cells Spirulina platensis (pH9.6) were studied by using a UV-VIS spectrophotometer. Also biosorption of these ions with cyanobacteria Spirulina platensis were studied using equilibrium dialysis and atomic absorption analysis.It was shown, that the absorption intensity of Spirulina platensis decreases, when Cr(III), Cr(VI), Cu(II) ions are added. Significant difference between the absorption intensity for Cu(II) Sp...

  12. Finite difference simulation of biological chromium (VI) reduction in ...

    African Journals Online (AJOL)

    2013-05-08

    May 8, 2013 ... precipitates of reduced chromium produce toxic sludge that may be difficult to remediate (Gonzalez et al., 2003; Blowes, 2002). Recent studies have shown the possibility of using locally isolated organisms to treat Cr(VI) contaminated groundwater and/or soil. The treatment can be implemented ex situ ...

  13. Population Changes in a Community of Alkaliphilic Iron-Reducing Bacteria Due to Changes in the Electron Acceptor: Implications for Bioremediation at Alkaline Cr(VI)-Contaminated Sites.

    Science.gov (United States)

    Fuller, Samuel J; Burke, Ian T; McMillan, Duncan G G; Ding, Weixuan; Stewart, Douglas I

    A serial enrichment culture has been grown in an alkaline Fe(III)-citrate-containing medium from an initial inoculum from a soil layer beneath a chromium ore processing residue (COPR) disposal site where Cr(III) is accumulating from Cr(VI) containing leachate. This culture is dominated by two bacterial genera in the order Clostridiales, Tissierella, and an unnamed Clostridium XI subgroup. This paper investigates the growth characteristics of the culture when Cr(VI) is added to the growth medium and when aquifer sand is substituted for Fe(III)-citrate. The aim is to determine how the availability and chemical form of Fe(III) affects the growth of the bacterial consortium, to determine the impact of Cr(VI) on growth, and thus attempt to understand the factors that are controlling Cr(III) accumulation beneath the COPR site. The culture can grow fermentatively at pH 9.2, but growth is stronger when it is associated with Fe(III) reduction. It can withstand Cr(VI) in the medium, but growth only occurs once Cr(VI) is removed from solution. Cr(VI) reduced the abundance of Tissierella sp. in the culture, whereas the Clostridium XI sp. was Cr(VI) tolerant. In contrast, growth with solid phase Fe(III)-oxyhydroxides (present as coatings on aquifer sand) favoured the Tissierella C sp., possibly because it produces riboflavin as an extracellular electron shuttling compound allowing more efficient electron transfer to solid Fe(III) phases. Thus, it is suggested that bacterially mediated Cr(III) reduction in the soil beneath the COPR site is dependent on Fe(III) reduction to sustain the bacterial community.

  14. The Ability of Benzoic Acid to Reduce Cr(VI Heavy Metal Content in Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Anugrah Windy Mustikarini

    2015-12-01

    Full Text Available Chromium (VI is an ionic heavy metal which has to be handled properly when dissolved in water due to its toxicity, corosive, carsinogenic activity.. According to the State Minister for Population and Environment’s regulation, the quality standards of waste water, which is allowed to be discharge on surface water contains Cr(VI is 0.05-1 mg/L. This research used benzoic acid which is a kind of organic acid to reduce Cr(VI content in water. Benzoic acid has an active carboxyl group which interact this metal. This paper, the elimination of Cr(VI using benzoic acid is undertaken through pH adjustment by regulating with phosphoric acid. The result showed the best condition to reducing Cr(VI content 41.99% when 400 ppm of benzoic acid and pH 7 was applied, respectively.

  15. Reactivity enhancement of iron sulfide nanoparticles stabilized by sodium alginate: Taking Cr (VI) removal as an example.

    Science.gov (United States)

    Wu, Jun; Wang, Xian-Bin; Zeng, Raymond J

    2017-07-05

    The widespread distribution of chromium(VI) in the environment leads to groundwater contamination. The use of iron sulfide (FeS) to remove Cr(VI) has therefore been proposed. However, aggregation is one of the main problems associated with the use of FeS nanoparticles prepared by traditional methods In this study, we used sodium alginate (SA) to stabilize FeS nanoparticles (FeS-SA). SA could prevent aggregation of FeS by the concurrent electrostatic repulsion and steric hindrance. Homogeneously dispersed FeS-SA nanoparticles 100nm in diameter were observed. FeS-SA showed high efficiency in Cr(VI) removal, corresponding to an enhancement of efficiency from 65% (7.50mmol Cr(VI) per g FeS) to 100% (11.54mmol Cr per g FeS) relative to that achieved with naked FeS. Analysis of reaction products by X-ray diffraction and X-ray photoelectron spectroscopy revealed the co-existence of α-FeOOH, S8, and Cr(OH)3 that apparently were introduced by Fe(II), S(-II), and Cr(VI), respectively. In-depth analysis of the removal mechanism revealed that reduction and adsorption respectively account for 82% and 18% of the Cr removal. In addition, higher pH and CaCl2 concentration resulted in lower removal efficiency. This study provides a promising application of SA in enhancing FeS reactivity for the remediation of groundwater pollution. Copyright © 2017 Elsevier B.V. All rights reserved.

  16. Reactivity enhancement of iron sulfide nanoparticles stabilized by sodium alginate: Taking Cr (VI) removal as an example

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Jun; Wang, Xian-Bin; Zeng, Raymond J., E-mail: rzeng@ustc.edu.cn

    2017-07-05

    Highlights: • Sodium alginate can be used to stabilize FeS nanoparticles. • FeS-SA enhances Cr(VI) removal efficiency from 65% to 100% compared to naked FeS. • Reduction and adsorption respectively account for 82% and 18% of Cr removal by FeS-SA. • Analysis of reaction products reveals the co-existence of α-FeOOH, S{sub 8}, and Cr(OH){sub 3.} - Abstract: The widespread distribution of chromium(VI) in the environment leads to groundwater contamination. The use of iron sulfide (FeS) to remove Cr(VI) has therefore been proposed. However, aggregation is one of the main problems associated with the use of FeS nanoparticles prepared by traditional methods In this study, we used sodium alginate (SA) to stabilize FeS nanoparticles (FeS-SA). SA could prevent aggregation of FeS by the concurrent electrostatic repulsion and steric hindrance. Homogeneously dispersed FeS-SA nanoparticles 100 nm in diameter were observed. FeS-SA showed high efficiency in Cr(VI) removal, corresponding to an enhancement of efficiency from 65% (7.50 mmol Cr(VI) per g FeS) to 100% (11.54 mmol Cr per g FeS) relative to that achieved with naked FeS. Analysis of reaction products by X-ray diffraction and X-ray photoelectron spectroscopy revealed the co-existence of α-FeOOH, S{sub 8}, and Cr(OH){sub 3} that apparently were introduced by Fe(II), S(−II), and Cr(VI), respectively. In-depth analysis of the removal mechanism revealed that reduction and adsorption respectively account for 82% and 18% of the Cr removal. In addition, higher pH and CaCl{sub 2} concentration resulted in lower removal efficiency. This study provides a promising application of SA in enhancing FeS reactivity for the remediation of groundwater pollution.

  17. Application of chromium stable isotopes to the evaluation of Cr(VI) contamination in groundwater and rock leachates from central Euboea and the Assopos basin (Greece)

    DEFF Research Database (Denmark)

    Economou-Eliopoulos, Maria; Frei, Robert; Atsarou, Cathy

    2014-01-01

    , stable chromium isotopes (expressed as δ53Cr values) were measured in groundwater and leachates in order to identify potential sources for Cr-contamination. The higher Cr(VI) concentrations in soil leachates compared to those in the rock pulp leachates potentially can be explained by the presence......Major and trace elements (a) in groundwater, ultramafic rocks from natural outcrops and soil samples from cultivated sites of Central Euboea and Assopos basin, and (b) in experimentally produced laboratory water leachates of rocks and soils were investigated by SEM/EDS, XRD and ICP/MS. In addition......(III). Using a Rayleigh distillation model and different fractionation factors of Cr(VI) reduction valid for aqueous Fe(II) and Fe(II)-bearing minerals, we calculate that more than ~ 53%, but maximum ~ 94%, of the originally mobile Cr(VI) pool was reduced to immobile Cr(III) in the waters investigated...

  18. Genesis of Cr(VI) in Sri Lankan soils and its adsorptive removal by calcined gibbsite

    Science.gov (United States)

    Rajapaksha, A. U.; Wijesundara, D. M.; Vithanage, M. S.; Ok, Y. S.

    2012-12-01

    Hexavalent chromium is highly toxic to biota and considered as a priority pollutant. Industrial sources of Cr(VI) include leather tanning, plating, electroplating, anodizing baths, rinse waters, etc. In addition, weathering of ultramafic rocks rich in chromium, such as serpentine, is known to Cr(VI) sources into natural water. The Cr(III) is the most stable in the environment, however, conversion of Cr(III) into Cr(VI) occurs in soil due to presence of naturally occurring minerals such as manganese dioxides. We investigated the amount of Cr(VI) recorded from the soils from anthropogenically and naturally contaminated soils (serpentine soils) in Sri Lanka and the removal efficacy of Cr(VI) by calcined gibbsite (Al oxides). The effect of pH on Cr(VI) adsorption was determined by adjusting the pH in the range of 4-10. In the experiments, the adsorbent concentration was kept at 1 g/l of solution containing 10 mg/l Cr(VI) at 25 0C. Total chromium recorded were around 11,000 mg kg-1 and 6,000 mg kg-1 for serpentine soil and tannery waste-contaminated soil, respectively. Although total Cr was high in the contaminated soils, Cr(VI) concentration was only about 28 mg kg-1 and 210 mg kg-1 in the serpentine and tannery soils, respectively. The calcined gibbsite has maximum adsorption of 85 % around pH 4 and adsorption generally decreased with increase of pH.

  19. Mechanistic insight into chromium(VI) reduction by oxalic acid in the presence of manganese(II)

    Energy Technology Data Exchange (ETDEWEB)

    Wrobel, Katarzyna; Corrales Escobosa, Alma Rosa; Gonzalez Ibarra, Alan Alexander; Mendez Garcia, Manuel; Yanez Barrientos, Eunice; Wrobel, Kazimierz, E-mail: kazimier@ugto.mx

    2015-12-30

    Over the past few decades, reduction of hexavalent chromium (Cr(VI)) has been studied in many physicochemical contexts. In this research, we reveal the mechanism underlying the favorable effect of Mn(II) observed during Cr(VI) reduction by oxalic acid using liquid chromatography with spectrophotometric diode array detector (HPLC–DAD), nitrogen microwave plasma atomic emission spectrometry (HPLC–MP-AES), and high resolution mass spectrometry (ESI–QTOFMS). Both reaction mixtures contained potassium dichromate (0.67 mM Cr(VI)) and oxalic acid (13.3 mM), pH 3, one reaction mixture contained manganese sulfate (0.33 mM Mn(II)). In the absence of Mn(II) only trace amounts of reaction intermediates were generated, most likely in the following pathways: (1) Cr(VI) → Cr(IV) and (2) Cr(VI) + Cr(IV) → 2Cr(V). In the presence of Mn(II), the active reducing species appeared to be Mn(II) bis-oxalato complex (J); the proposed reaction mechanism involves a one-electron transfer from J to any chromium compound containing Cr=O bond, which is reduced to Cr−OH, and the generation of Mn(III) bis-oxalato complex (K). Conversion of K to J was observed, confirming the catalytic role of Mn(II). Since no additional acidification was required, the results obtained in this study may be helpful in designing a new, environmentally friendly strategy for the remediation of environments contaminated with Cr(VI).

  20. Synergically Improving Light Harvesting and Charge Transportation of TiO2 Nanobelts by Deposition of MoS2 for Enhanced Photocatalytic Removal of Cr(VI

    Directory of Open Access Journals (Sweden)

    Jie Liu

    2017-01-01

    Full Text Available Herein, MoS2/TiO2 nanobelts heterojunction have been successfully synthesized by in situ growth method for photocatalytic reduction of Cr(VI. TiO2 nanobelts (NBs with rough surface were prepared firstly by acidic treatment process, which is beneficial for deposition and growth of MoS2 to form heterojunctions. As a result of special energy level offset and nanostructure, MoS2/TiO2 NBs composite were endowed with higher light-harvesting capacity and charge transportation efficiency, which are indispensible merits for excellent photocatalytic activity. The photocatalytic reduction of Cr(VI reveals that the synthesized MoS2/TiO2 NBs composite have superior photocatalytic ability than other samples. Meanwhile, a photoreduction mechanism is proposed based on the systematic investigation, where the photogenerated electrons are demonstrated as the dominant reductive species to reduce Cr(VI to Cr(III.

  1. Polyacrylonitrile/manganese acetate composite nanofibers and their catalysis performance on chromium (VI) reduction by oxalic acid

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Chengcheng [Jilin University Alan G MacDiarmid Institute, Changchun 130012 (China); Li, Xiang, E-mail: xiangli@jlu.edu.cn [Jilin University Alan G MacDiarmid Institute, Changchun 130012 (China); Bian, Xiujie; Zheng, Tian [Jilin University Alan G MacDiarmid Institute, Changchun 130012 (China); Wang, Ce, E-mail: cwang@jlu.edu.cn [Jilin University Alan G MacDiarmid Institute, Changchun 130012 (China)

    2012-08-30

    Highlights: Black-Right-Pointing-Pointer We have successfully prepared PAN/Mn(CH{sub 3}COO){sub 2} composite nanofibers. Black-Right-Pointing-Pointer The nanofibers exhibit excellent catalysis performance for Cr(VI) reduction. Black-Right-Pointing-Pointer The nanofibers are effective and environment-friendly materials to remove Cr(VI). - Abstract: Polyacrylonitrile(PAN)/manganese acetate(Mn(CH{sub 3}COO){sub 2}) composite nanofibers have been fabricated by electrospinning, a simple and effective technology. The obtained composite nanofibers were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and Fourier transform infrared spectrometer (FT-IR). The composite nanofibers are amorphous in structure, continuous, even and smooth. At the same time, the reduction performance of Cr(VI) by oxalic acid in the presence of the composite nanofibers is also investigated. The results indicate that the composite nanofibers have exhibited excellent catalysis performance for Cr(VI) reduction from a Cr{sub 2}O{sub 7}{sup 2-}-containing solution by oxalic acid. And the critical parameters, such as the catalyst dosage, oxalic acid content, chromium concentration, the pH value of the reaction solution and light have important impact on the reduction process. Under the simulated solar light irradiation, after only 60 min, 1.2 mM initial Cr(VI) solution was reduced absolutely in the presence of PAN/Mn(CH{sub 3}COO){sub 2} composite nanofibers containing 17.5 wt.% Mn(CH{sub 3}COO){sub 2} by 0.3 mL 0.5 M oxalic acid. In light, the reduction of Cr(VI) by oxalic acid is markedly accelerated.

  2. Introduction of Hydrogen Peroxide as an Oxidant in Flow Injection Analysis: Speciation of Cr(III) and Cr(VI)

    DEFF Research Database (Denmark)

    Andersen, Jens Enevold Thaulov

    1998-01-01

    Hydrogen peroxide was used as an oxidant in Flow Injection Analysis (FIA). The formation of gaseous components during the analysis was suppressed by maintaining a concentration lower than 0.15% of hydrogen peroxide in 0.1 M NaOH. By this method Cr(III) was oxidised on-line to Cr(VI) which...

  3. Speciation of Cr(VI) in environmental samples in the vicinity of the ferrochrome smelter

    Energy Technology Data Exchange (ETDEWEB)

    Sedumedi, Hilda N. [Department of Chemistry, Tshwane University of Technology, P.O. Box 56208, Arcadia, 0007, Pretoria (South Africa); Mandiwana, Khakhathi L., E-mail: MandiwanaKL@tut.ac.za [Department of Chemistry, Tshwane University of Technology, P.O. Box 56208, Arcadia, 0007, Pretoria (South Africa); Ngobeni, Prince; Panichev, Nikolay [Department of Chemistry, Tshwane University of Technology, P.O. Box 56208, Arcadia, 0007, Pretoria (South Africa)

    2009-12-30

    The impact of ferrochrome smelter on the contamination of its environment with toxic hexavalent chromium, Cr(VI), was assessed by analyzing smelter dusts, soil, grass and tree barks. For the separation of Cr(VI) from Cr(III), solid samples were treated with 0.1 M Na{sub 2}CO{sub 3} and filtered through hydrophilic PDVF 0.45 {mu}m filter prior to the determination of Cr(VI) by electrothermal atomic absorption spectrometry (ET-AAS). Ferrochrome smelter dust was found to contain significant levels of Cr(VI), viz. 43.5 {mu}g g{sup -1} (cyclone dust), 2710 {mu}g g{sup -1} (fine dust), and 7800 {mu}g g{sup -1} (slimes dust) which exceeded the maximum acceptable risk concentration (20 {mu}g g{sup -1}). The concentration of Cr(VI) in environmental samples of grass (3.4 {+-} 0.2), soil (7.7 {+-} 0.2), and tree bark (11.8 {+-} 1.2) collected in the vicinity of the chrome smelter were higher as compared with the same kind of samples collected from uncontaminated area. The results of the investigation show that ferrochrome smelter is a source of environmental pollution with contamination factors of Cr(VI) ranging between 10 and 50.

  4. Removal of Cr(VI) from Aqueous Environments Using Micelle-Clay Adsorption

    Science.gov (United States)

    Qurie, Mohannad; Khamis, Mustafa; Manassra, Adnan; Ayyad, Ibrahim; Nir, Shlomo; Scrano, Laura; Bufo, Sabino A.; Karaman, Rafik

    2013-01-01

    Removal of Cr(VI) from aqueous solutions under different conditions was investigated using either clay (montmorillonite) or micelle-clay complex, the last obtained by adsorbing critical micelle concentration of octadecyltrimethylammonium ions onto montmorillonite. Batch experiments showed the effects of contact time, adsorbent dosage, and pH on the removal efficiency of Cr(VI) from aqueous solutions. Langmuir adsorption isotherm fitted the experimental data giving significant results. Filtration experiments using columns filled with micelle-clay complex mixed with sand were performed to assess Cr(VI) removal efficiency under continuous flow at different pH values. The micelle-clay complex used in this study was capable of removing Cr(VI) from aqueous solutions without any prior acidification of the sample. Results demonstrated that the removal effectiveness reached nearly 100% when using optimal conditions for both batch and continuous flow techniques. PMID:24222757

  5. Kinetic and Thermodynamic Studies of the Adsorption of Cr(VI) onto ...

    African Journals Online (AJOL)

    AKS), Juniperus procera sawdust (JPS) and papaya peels (PP) were investigated as adsorbents for the removal of Cr(VI). The study employed a batch method to investigate the efficiency of the adsorbents. Parameters that influence adsorption ...

  6. Removal of Cr(VI from Aqueous Environments Using Micelle-Clay Adsorption

    Directory of Open Access Journals (Sweden)

    Mohannad Qurie

    2013-01-01

    Full Text Available Removal of Cr(VI from aqueous solutions under different conditions was investigated using either clay (montmorillonite or micelle-clay complex, the last obtained by adsorbing critical micelle concentration of octadecyltrimethylammonium ions onto montmorillonite. Batch experiments showed the effects of contact time, adsorbent dosage, and pH on the removal efficiency of Cr(VI from aqueous solutions. Langmuir adsorption isotherm fitted the experimental data giving significant results. Filtration experiments using columns filled with micelle-clay complex mixed with sand were performed to assess Cr(VI removal efficiency under continuous flow at different pH values. The micelle-clay complex used in this study was capable of removing Cr(VI from aqueous solutions without any prior acidification of the sample. Results demonstrated that the removal effectiveness reached nearly 100% when using optimal conditions for both batch and continuous flow techniques.

  7. Biosorption of Cr(VI from Aqueous Solution Using Murraya koenigii (Curry tree Stems

    Directory of Open Access Journals (Sweden)

    Selvaraj Suresh

    2016-12-01

    Full Text Available In the present work, the sorption capacity of Murraya Koenigii Stems (MKST, an agricultural waste, is identified for the removal of Cr(VI from aqueous solution and the effect of different process parameters likes pH and adsorbent dosage were studied. pH 1 is observed to be the optimum pH for Cr(VI sorption onto the biosorbent. The equilibrium data of Cr(VI sorption fit well with the Langmuir model with a monolayer sorption capacity of 12.25 mg/g. The results show that the metal ion interacts strongly with the biosorbent and can be effectively used in the removal of Cr(VI from aqueous solution. DOI: http://dx.doi.org/10.17807/orbital.v0i0.867

  8. Exfoliated polypyrrole-organically modified montmorillonite clay nanocomposite as a potential adsorbent for Cr (VI) removal

    CSIR Research Space (South Africa)

    Setshedi, KZ

    2013-01-01

    Full Text Available Exfoliated polypyrrole-organically modified montmorillonite clay nanocomposite (PPy OMMT NC), was prepared as a potential adsorbent, via in situ polymerization of pyrrole monomer for adsorption of toxic Cr(VI) from aqueous solution. The WAXD...

  9. Cr(VI) Adsorption on Red Mud Modified by Lanthanum: Performance, Kinetics and Mechanisms

    OpenAIRE

    Cui, You-Wei; Li, Jie; Du, Zhao-Fu; Peng, Yong-Zhen

    2016-01-01

    Water pollution caused by the highly toxic metal hexavalent chromium (Cr(VI)) creates significant human health and ecological risks. In this study, a novel adsorbent was used to treat Cr(VI)-containing wastewater; the adsorbent was prepared using red mud (RM) generated from the alumina production industry and the rare earth element lanthanum. This study explored adsorption performance, kinetics, and mechanisms. Results showed that the adsorption kinetics of the RM modified by lanthanum (La-RM...

  10. Synthesis and application of magnetic hydrogel for Cr(VI) removal from contaminated water

    KAUST Repository

    Tang, Samuel C N

    2010-11-01

    Many magnetic adsorbents reported in the literature, such as iron oxides, for Cr(VI) removal have been found effective only in low pH environments. Moreover, the application of polymeric hydrogels on heavy metal removal has been hindered by difficulties in separation by filtration. In this study, a magnetic cationic hydrogel was synthesized for Cr(VI) removal from contaminated water, making use of the advantages of magnetic adsorbents and polymeric hydrogels. The magnetic hydrogel was produced by imbedding 10-nm γ-Fe2O 3 nanoparticles into the polymeric matrix via radical polymerization. Characterization of the hydrogel was undertaken with Fourier transform infrared and vibrating sample magnetometer; swelling properties were tested and anionic adsorption capacity was evaluated. The magnetic hydrogel showed a superior Cr(VI) removal capacity compared to commercial products such as MIEX®. Cr(VI) removal was independent of solution pH. Results show that Cr(VI) removal kinetics was improved drastically by grinding the bulk hydrogel into powder form. At relevant concentrations, common water anions (e.g., Cl-, SO4 2-, PO4 3-) and natural organic matter did not exhibit significant inhibition of Cr(VI) adsorption onto the hydrogel. Results of vibrating sample magnetometer indicate that the magnetic hydrogel can be easily separated from treatment systems. Regeneration of the magnetic hydrogel can be easily achieved by washing the Cr(VI)-loaded hydrogel with 0.5 M NaCl solution, with a recovery rate of about 90% of Cr(VI). © Copyright 2010, Mary Ann Liebert, Inc. 2010.

  11. Adsorption behavior of carboxylated cellulose nanocrystal-polyethyleneimine composite for removal of Cr(VI) ions

    Science.gov (United States)

    Liu, Chao; Jin, Ru-Na; Ouyang, Xiao-kun; Wang, Yang-Guang

    2017-06-01

    In this study, a composite adsorbent (CCN-PEI) composed of carboxylated cellulose nanocrystals (CCN) and polyethyleneimine (PEI) was prepared through an amidation reaction between the carboxyl groups of the CCN and the amine groups of the PEI. The adsorption performance of the CCN-PEI was tested by removing Cr(VI) ions from aqueous solutions. The physicochemical properties of the CCN and the Cr(VI) ion-loaded CCN-PEI were studied using scanning electron microscopy (SEM), transmission electron microscopy, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy. To investigate the adsorption kinetics of Cr(VI) ions onto this newly developed CCN-PEI, we performed experiments under different adsorption conditions, by varying the contact time, solution pH, initial Cr(VI) ion concentration, and adsorption temperature. The prepared CCN-PEI exhibited an encouraging uptake capacity of 358.42 mg × g-1. The adsorption process was fast: within the first 100 min, Cr(VI) ion adsorption onto the CCN-PEI was about 65%, and the adsorption equilibrium was reached within 250 min. Kinetics experiments indicated that the adsorption process could be described by a pseudo-second-order kinetic model. Furthermore, our adsorption equilibrium data fit the Langmuir isotherms well. The calculated thermodynamic parameters, such as the free energy change (ΔG = -2.93 kJ × mol-1), enthalpy change (ΔH = -5.69 kJ × mol-1), and entropy change (ΔS = -9.14 kJ × mol-1), indicate that the adsorption of Cr(VI) ions onto CCN-PEI was a spontaneous exothermic process. Regeneration tests indicated that CCN-PEI showed good durability and good efficiency for repeated Cr(VI) adsorptions. Based on the results obtained in this work, it can be concluded that CCN-PEI is a potentially effective adsorbent for removing Cr(VI) ions from aqueous solutions.

  12. Abatement of toxicity of effluents containing Cr(VI) by heterogeneous photocatalysis. Toxicity assessment by AMPHITOX assay.

    Science.gov (United States)

    Hojman, Jonatan Y; Meichtry, J Martín; Litter, Marta I; Pérez Coll, Cristina S

    2015-12-01

    Toxicity of a Cr(VI) solution before and after treatment by TiO2 heterogeneous photocatalysis (HP) was performed with AMPHITOX bioassay. Changes in toxicity on Rhinella arenarum larvae for 10-d were monitored after exposure to an untreated Cr(VI) solution and to the same solution after HP treatment. The HP treatment of a 41.60 mg L(-1) Cr(VI) solution reduced to 37.5% the concentration of the metal ion. A 10-fold reduction in toxicity at acute exposure (72 h) and 150-fold reduction in toxicity after 240 h was found. Further, the LOEC value increased from 0.001% for the untreated solution to 0.153% after HP treatment. Moreover, the safe concentration in untreated solution corresponded to 0.0001% sample, and it was 0.01% after the treatment, i.e., 100 times higher. A saving of water of about 100,000 L per L of effluent would be possible through dilution to allow safer concentrations for discharge; the saving would reach the highest value (1,000,000 L per L) at 240 h. Sub-lethal effects were completely absent in larvae exposed to the treated solution. The AMPHITOX test allowed to detect chronic effects at low Cr concentrations, i.e. at environmentally relevant levels. Copyright © 2015 Elsevier Inc. All rights reserved.

  13. Novel lignocellulosic wastes for comparative adsorption of Cr(VI: equilibrium kinetics and thermodynamic studies

    Directory of Open Access Journals (Sweden)

    Haroon Hajira

    2017-06-01

    Full Text Available Cr(VI adsorption was studied for abundantly available low-cost lignocellulosic adsorbents in Pakistan namely, tobacco stalks (TS, white cedar stem (WCS and eucalyptus bark (EB. Several process variables like contact time, adsorbent dose, pH, metal concentration, particle size and temperature were optimized in batch mode. EB showed high Cr(VI adsorption of 63.66% followed by WCS 62% and TS 57% at pH 2, which is higher than most of the reported literature. Langmuir isotherm (R2 = 0.999 was well fitted into the equilibrium Cr(VI data of EB, suggesting homogeneous active sites and monolayer coverage of Cr(VI onto the EB surface. Freundlich (R2 = 0.9982 isotherm was better fitted to the equilibrium data of TS and WCS, revealing the adsorption sites with heterogeneous energy distribution and multilayer Cr(VI adsorption. Moreover, the Cr(VI adsorption of studied adsorbents followed the pseudo-second order kinetic model. Thermodynamic properties were investigated in two temperature ranges, i.e., T1 (303–313 K and T2 (313–323 K. TS and EB showed the exothermic at T1 and endothermic reactions at T2 with entropy controlled adsorption at the solid-liquid interface, and WCS exhibited an opposite thermal trend with decreasing disorderness at solid-liquid interface as temperature rises. Gibbs free energy (ΔG>0 confirmed the non-spontaneous adsorption process for all studied adsorbents.

  14. Adsorption of Cr(VI onto Hybrid Membrane of Carboxymethyl Chitosan and Silicon Dioxide

    Directory of Open Access Journals (Sweden)

    Yanling Deng

    2017-01-01

    Full Text Available In this study, a new adsorbent material was synthesized by using carboxymethyl chitosan and silicon dioxide. The hybrid membrane was used as an adsorbent for the removal of Cr(VI from aqueous solutions. The adsorption potential of Cr(VI by the hybrid materials was investigated by varying experimental conditions such as pH, contact time, and the dosage of the hybrid membrane. Adsorption isotherms of Cr(VI onto the hybrid membrane were studied with varying initial concentrations under optimum experiment conditions. The surface property of the hybrid membrane was characterized by SEM (scanning electron microscope and Fourier transform infrared spectrometer (FTIR. The concentrations of Cr(VI in solution are determined by ICP-AES (inductively coupled plasma atomic emission spectrometry. The present study investigates the adsorption mechanisms of Cr(VI onto the hybrid membrane. The results provide new insight, demonstrating that the modified hybrid membrane can be an efficient adsorbent for Cr(VI from the aqueous solution.

  15. Chromium Biosorption from Cr(VI) Aqueous Solutions by Cupressus lusitanica Bark: Kinetics, Equilibrium and Thermodynamic Studies

    OpenAIRE

    Alma Rosa Netzahuatl-Muñoz; María del Carmen Cristiani-Urbina; Eliseo Cristiani-Urbina

    2015-01-01

    The present study investigated the kinetics, equilibrium and thermodynamics of chromium (Cr) ion biosorption from Cr(VI) aqueous solutions by Cupressus lusitanica bark (CLB). CLB total Cr biosorption capacity strongly depended on operating variables such as initial Cr(VI) concentration and contact time: as these variables rose, total Cr biosorption capacity increased significantly. Total Cr biosorption rate also increased with rising solution temperature. The pseudo-second-order model describ...

  16. Heavy Metal Resistances and Chromium Removal of a Novel Cr(VI)-Reducing Pseudomonad Strain Isolated from Circulating Cooling Water of Iron and Steel Plant.

    Science.gov (United States)

    Zhang, Jian-Kun; Wang, Zhen-Hua; Ye, Yun

    2016-12-01

    Three bacterial isolates, GT2, GT3, and GT7, were isolated from the sludge and water of a circulating cooling system of iron and steel plant by screening on Cr(VI)-containing plates. Three isolates were characterized as the members of the genus Pseudomonas on the basis of phenotypic characteristics and 16S rRNA sequence analysis. All isolates were capable of resisting multiple antibiotics and heavy metals. GT7 was most resistant to Cr(VI), with a minimum inhibitory concentration (MIC) of 6.5 mmol L(-1). GT7 displayed varied rates of Cr(VI) reduction in M2 broth, which was dependent on pH, initial Cr(VI) concentration, and inoculating dose. Total chromium analysis revealed that GT7 could remove a part of chromium from the media, and the maximum rate of chromium removal was up to 40.8 %. The Cr(VI) reductase activity of GT7 was mainly associated with the soluble fraction of cell-free extracts and reached optimum at pH 6.0∼8.0. The reductase activity was apparently enhanced by external electron donors and Cu(II), whereas it was seriously inhibited by Hg(II), Cd(II), and Zn(II). The reductase showed a K m of 74 μmol L(-1) of Cr(VI) and a V max of 0.86 μmol of Cr(VI) min(-1) mg(-1) of protein. The results suggested that GT7 could be a promising candidate for in situ bioremediation of Cr(VI).

  17. Immobilization of Cr(Vi) as a contaminant from soil by iron compounds; Inmovilizacion de Cr(VI) como contaminante del suelo por compuestos de hierro

    Energy Technology Data Exchange (ETDEWEB)

    Marin A, M. de J.; Romero G, E. T. [ININ, Carretera Mexico-Toluca s/n, Ocoyoacac 52750, Estado de Mexico (Mexico); Reyes G, L. R. [Universidad Autonoma del Estado de Hidalgo, Centro de Investigacion en Ciencias de la Tierra, Carretera Pachuca-Tulancingo Km. 4.5, Pachuca 42184, Hidalgo (Mexico)], e-mail: elizabeth.romero@inin.gob.mx

    2008-07-01

    The objective of this research was to determine the physicochemical and surface properties of Fe{sup 0} and FeS to select the appropriate radioactive material for use in the design of artificial barriers or walls and remove Cr (Vi). The physicochemical characterization was carried out of iron: Fe{sup 0} and FeS, using scanning electron microscopy of high vacuum, X-ray diffraction and thermal gravimetric analysis techniques. As for the characterization of the surface, was used to determine the surface area, point of zero charge, density of active sites and kinetics of moisture. We obtained a solution of Cr (Vi) by elution of deionized water on the pollution land of Buenavista, Guanajuato. The concentration of Cr (Vi) from a stock solution was 55.56 mg / L determined by UV-Vis spectrophotometry. Stripping or maximum immobilization of Cr (Vi) with Fe{sup 0} (material chosen by their physicochemical and surface properties) was 68.25% using Fe{sup 0}, at a concentration less than 0.1, ph equal to 3 and a contact time of 24 hours. (Author)

  18. Simultaneous removal of Cr(VI) and 4-chlorophenol through photocatalysis by a novel anatase/titanate nanosheet composite: Synergetic promotion effect and autosynchronous doping

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Wen, E-mail: wzl0025@auburn.edu [Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control, School of Environmental Science and Engineering, Nanjing University of Information Science and Technology, Nanjing 210044 (China); The Key Laboratory of Water and Sediment Sciences, Ministry of Education, Department of Environmental Engineering, Peking University, Beijing 100871 (China); Environmental Engineering Program, Department of Civil Engineering, Auburn University, Auburn, AL 36849 (United States); Sun, Weiling [The Key Laboratory of Water and Sediment Sciences, Ministry of Education, Department of Environmental Engineering, Peking University, Beijing 100871 (China); Borthwick, Alistair G.L. [School of Engineering, The University of Edinburgh, The King’s Buildings, Edinburgh EH9 3JL (United Kingdom); Wang, Ting [The Key Laboratory of Water and Sediment Sciences, Ministry of Education, Department of Environmental Engineering, Peking University, Beijing 100871 (China); Li, Fan [Environmental Engineering Program, Department of Civil Engineering, Auburn University, Auburn, AL 36849 (United States); Guan, Yidong, E-mail: yidongguan@nuist.edu.cn [Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control, School of Environmental Science and Engineering, Nanjing University of Information Science and Technology, Nanjing 210044 (China); Environmental Engineering Program, Department of Civil Engineering, Auburn University, Auburn, AL 36849 (United States)

    2016-11-05

    Highlights: • TNS composed of anatase and titanate synthesized via a facile one-step method. • Cr(VI) and 4-CP can be simultaneously removed by TNS through photocatalysis. • Photocatalytic efficiencies of Cr(VI) and 4-CP greatly enhanced when coexisting. • Synergetic promotion effect occurs due to separation of electron-hole pairs. • Autosynchronous doping after Cr(III) adsorption leads to narrowed energy gap. - Abstract: Clean-up of wastewaters with coexisting heavy metals and organic contaminants is a huge issue worldwide. In this study, a novel anatase/titanate nanosheet composite material (labeled as TNS) synthesized through a one-step hydrothermal reaction was demonstrated to achieve the goal of simultaneous removal of Cr(VI) and 4-cholophenol (4-CP) from water. TEM and XRD analyses indicated the TNS was a nano-composite of anatase and titanate, with anatase acting as the primary photocatalysis center and titanate as the main adsorption site. Enhanced photocatalytic removal of co-existent Cr(VI) and 4-CP was observed in binary systems, with apparent rate constants (k{sub 1}) for photocatalytic reactions of Cr(VI) and 4-CP about 3.1 and 2.6 times of that for single systems. In addition, over 99% of Cr(VI) and 4-CP was removed within 120 min through photocatalysis by TNS at pH 7 in the binary system. Mechanisms for enhanced photocatalytic efficiency in the binary system are identified as: (1) a synergetic effect on the photo-reduction of Cr(VI) and photo-oxidation of 4-CP due to efficient separation of electron-hole pairs, and (2) autosynchronous doping because of reduced Cr(III) adsorption onto TNS. Furthermore, TNS could be efficiently reused after a simple acid-base treatment.

  19. Adsorption studies for the removal of Cr(VI) ion from aqueous solution

    African Journals Online (AJOL)

    The adsorption characteristics of Cr(VI) in the form of Cr2O7(-2) ion from aqueous solution onto synthetic exchanger Amberlite IRA 400(Cl) resin was studied from UV – visible spectrphotometric measurement using DPC at 580nm. The efficiency of the adsorbent was judged from the variation of the % adsorption with (i) ...

  20. Different ATM Signaling in Response to Chromium(VI) Metabolism via Ascorbate and Nonascorbate Reduction: Implications for in Vitro Models and Toxicogenomics.

    Science.gov (United States)

    Luczak, Michal W; Green, Samantha E; Zhitkovich, Anatoly

    2016-01-01

    Carcinogenic hexavalent chromium [Cr(VI)] requires cellular reduction to generate DNA damage. Metabolism of Cr(VI) by its principal reducer ascorbate (Asc) lacks a Cr(V) intermediate, which is abundant in reactions with a minor reducing agent, glutathione. Cultured cells are widely used in mechanistic studies of Cr(VI) toxicity; however, they typically contain ATM kinase, which controls DNA damage responses involving several hundreds of proteins. Treatment of standard cultures with Cr(VI) strongly activated ATM, as indicated by its automodification at Ser1981 and by phosphorylation of checkpoint kinase 2 (CHK2) and chromatin/transcription regulator KRAB-associated protein 1 (KAP1). Confirming the importance of activated ATM, its inhibition impaired replication recovery and clonogenic survival. In contrast, fully Asc-restored cells lacked ATM activation by Cr(VI), and ATM silencing produced no significant effects on p53 stabilization, apoptosis, replication recovery, or clonogenic survival. Dose dependence studies found a close correlation between ATM activation and the extent of Cr(VI) reduction by glutathione. Asc restoration in cultured cells dramatically altered their stress responses to Cr(VI) by preventing activation of the oxidant-sensitive ATM network. We suggest that toxicogenomic and other cell response-based approaches likely underestimate Cr(VI) genotoxicity when standard ATM-activating carcinogens are used as references. Luczak MW, Green SE, Zhitkovich A. 2016. Different ATM signaling in response to chromium(VI) metabolism via ascorbate and nonascorbate reduction: implications for in vitro models and toxicogenomics. Environ Health Perspect 124:61-66; http://dx.doi.org/10.1289/ehp.1409434.

  1. Biotreatment of Cr(VI) contaminated waters by sulphate reducing bacteria fed with ethanol

    Energy Technology Data Exchange (ETDEWEB)

    Pagnanelli, F., E-mail: francesca.pagnanelli@uniroma1.it [Department of Chemistry, Sapienza University of Rome, P.le Aldo Moro 5, 00185 Rome (Italy); Cruz Viggi, C., E-mail: carolina.cruzviggi@uniroma1.it [Department of Chemistry, Sapienza University of Rome, P.le Aldo Moro 5, 00185 Rome (Italy); Cibati, A., E-mail: alessio.cibati@uniroma1.it [Department of Chemistry, Sapienza University of Rome, P.le Aldo Moro 5, 00185 Rome (Italy); Uccelletti, D., E-mail: daniela.uccelletti@uniroma1.it [Department of Biology and Biotechnology, Sapienza University of Rome, P.le A. Moro 5, 00185 Rome (Italy); Toro, L., E-mail: luigi.toro@uniroma1.it [Department of Chemistry, Sapienza University of Rome, P.le Aldo Moro 5, 00185 Rome (Italy); Palleschi, C., E-mail: claudio.palleschi@uniroma1.it [Department of Biology and Biotechnology, Sapienza University of Rome, P.le A. Moro 5, 00185 Rome (Italy)

    2012-01-15

    Highlights: Black-Right-Pointing-Pointer Use of ethanol as electron donor for sulphate-reducing bacteria for the treatment of Cr(VI). Black-Right-Pointing-Pointer Isolation of contribution in Cr removal (adsorption vs. bioprecipitation). Black-Right-Pointing-Pointer Bioassessment of the process effectiveness by ecotoxicological in vivo tests using C. elegans. - Abstract: Biological treatment of Cr(VI) contaminated waters was performed in fixed bed reactors inoculated with SRB (sulphate-reducing bacteria) growing on ethanol. Treatment efficiency was evaluated by checking chemical abatement of Cr(VI) and by ecotoxicological tests using the nematode Caenorhabditis elegans. A preliminary comparison between ethanol and lactate was performed, denoting that using ethanol, the same values of final sulphate abatement were obtained. In addition ethanol showed to be a substrate more competitive than lactate in kinetic terms. Fixed bed column reactors were continuously fed with a solution containing sulphates (3 g L{sup -1}), ethanol (1.5 g L{sup -1}) and Cr(VI) (50 mg L{sup -1}). At steady state the column inoculated with SRB removed 65 {+-} 5% of sulphate and 95 {+-} 5% of chromium. Bioactive removal mechanisms predominated over biosorption. Diminution of Cr(VI) toxicity was assessed by using the nematode C. elegans as a test organism showing that the survival of nematodes was 20% in the presence of the untreated influent and raised up to 53% when the nematodes were exposed to the treated effluent.

  2. Removal of Cr(VI from Aqueous Solution Using Modified Pomegranate Peel : Equilibrium and Kinetic Studies

    Directory of Open Access Journals (Sweden)

    Tariq S. Najim

    2009-01-01

    Full Text Available The present investigation deals with the utilization of modified pomegrenate peel (MPGP and formaldehyde modified pomegrenate peel (FMPGP as adsorbents for the removal of chromium Cr(VI from aqueous solution. A series of experiments were conducted in a batch system to evaluate the effect of system variables. The effect of pH, initial Cr(VI concentration, contact time, adsorbent dosage and temperature were considered. The optimal pH values of Cr(VI removal by MPGP and FMPGP were 2.0 and 3.0 respectively. The time required for equilibrium was found to be about 100 minutes. The initial Cr(VI concentration and adsorbent dosage was found to have large effect on the adsorption of Cr(VI. The maximum uptake capacities were 13.01 and 22.28 mg of Cr(VI per gram of MPGP and FMPGP respectively. Adsorption kinetic data were tested using pseudo-first order, pseudo-second order, Elovich and intra-particle diffusion models. Kinetic studies showed that the adsorption followed a pseudo second order reaction due to the high correlation coefficient and the agreement between the experimental and calculated values of qe.The adsorption may follow intraparticle diffusion as well, due to the highest values of rate constants for the surface adsorption and intraparticle diffusion kinetic models, the higher values of rate constants are related to an improved bonding between Cr(VI ions and adsorbent particle.The Dubinin-radushkevich, Freundlich and Tempkin models were the closest fit for the equilibrium data of MPGP and FMPGP.

  3. Distinguished Cr(VI) capture with rapid and superior capability using polydopamine microsphere: Behavior and mechanism.

    Science.gov (United States)

    Zhang, Qingrui; Li, Yixuan; Yang, Qinggang; Chen, He; Chen, Xinqing; Jiao, Tifeng; Peng, Qiuming

    2018-01-15

    Toxic heavy metal containing Cr(VI) species is a serious threat for ecological environment and human beings. In this work, a new mussel-inspired polydopamine microsphere (PDA-sphere) is prepared through in situ oxidative polymerization at air condition with controllable sizes. The adsorption of Cr(VI) ions onto PDA-sphere is highly pH dependent with the optimal pH ranging from 2.5 to 3.8. A rapid Cr(VI) removal can approach in 8min for equilibrium. More importantly, the prepared materials exhibit a remarkable sorption selectivity, coexisting SO42-, NO3- and Cl- ions at high levels; The applicability model further proves its effective performances with treated capacity of 42,000kg/kg sorbent, and the effluent can be reduced from 2000ppb to below 50ppb, which meets the drinking water criterions recommended by WHO. 1kg sorbent can also purify approximately 100t Cr(VI) contaminated wastewaters basing on the wastewater discharges of China. Such capacity for application ranks the top level for Cr(VI) removal. Additionally, the exhausted materials can be well regenerated by binary alkaline and salts mixtures. Such efficient adsorption can be ascribed to the well-dispersed morphology as well as the strong affinity between Cr(VI) and catechol or amine groups by XPS investigation. All the results suggest that polydopamine microspheres may be ideal materials for Cr(VI) treatment in waters. Copyright © 2017 Elsevier B.V. All rights reserved.

  4. Cinética e equilíbrio de adsorção dos oxiânions Cr (VI, Mo (VI e Se (VI pelo sal de amônio quaternário de quitosana Kinetics and equilibrium of adsorption of oxyanions Cr (VI, Mo (VI and Se (VI by quaternary ammonium chitosan salt

    Directory of Open Access Journals (Sweden)

    Viviane A. Spinelli

    2005-07-01

    Full Text Available O sal quaternário de quitosana foi sintetizado com cloreto de glicidil trimetil amônio. A modificação química foi caracterizada por espectrometria no IV, RMN de 13C e ¹H, e mmol/g de grupos quaternários presentes na matriz polimérica por condutimetria. A remoção de Cr (VI, Mo (VI e Se (VI, em meio aquoso, foi investigada em processo de batelada. A adsorção mostrou ser dependente do pH para o Cr (VI e Se (VI, com um pH ótimo de adsorção, entre 4,0 a 6,0. Para o Mo (VI a adsorção manteve-se quase constante no intervalo de pH entre 4,0 e 11,5. O modelo de isoterma de Langmuir descreveu melhor os dados de equilíbrio na faixa de concentração investigada. No presente estudo, um grama do sal quaternário de quitosana reticulado com glutaraldeído adsorveu 68,3 mg de Cr, 63,4 mg de Mo e 90,0 mg de Se. A velocidade de adsorção, no processo, segue a equação cinética de pseudo segunda-ordem, sendo que o equilíbrio para os três íons foi alcançado próximo aos 200 minutos. A análise dispersiva de raios-X para o Cr (VI mostrou que o principal mecanismo de adsorção é a troca iônica entre os íons Cl- da superfície do polímero pelos oxiânions. O trocador aniônico apresentou a seguinte ordem de seletividade: Cr (VI > Mo (VI > Se (VI.Quaternary chitosan salt was synthesized in the presence of glycidyl trimetyl ammonium chloride. The polymer was characterized by spectroscopic techniques: infrared, 13C and ¹H NMR, while the amount of quaternary ammonium groups was obtained by condutimetry. The removal of Cr (VI, Mo (VI and Se (VI from aqueous solutions was carried out in batch adsorption processes. The process seemed to be pH dependent for Cr (VI and Se (VI with an optimum pH ranging from 4.0 to 6.0; while for Mo (VI the adsorption remained almost constant within the range between 4.0 and 11.5. The Langmuir isotherm model provided the best fit of the equilibrium data over the whole concentration investigated. In the experiment

  5. As(V)/Cr(VI) pollution control in soils, hemp waste, and other by-products: competitive sorption trials.

    Science.gov (United States)

    Quintáns-Fondo, Ana; Ferreira-Coelho, Gustavo; Paradelo-Núñez, Remigio; Nóvoa-Muñoz, Juan Carlos; Arias-Estévez, Manuel; Fernández-Sanjurjo, María José; Álvarez-Rodríguez, Esperanza; Núñez-Delgado, Avelino

    2016-10-01

    We study As(V)/Cr(VI) competitive sorption on a forest soil, a vineyard soil, pyritic material, mussel shell, pine bark, oak ash, and hemp waste, adding variable As(V) and Cr(VI) concentrations or displacing each pollutant with the same concentration of the other. When using variable concentrations, As(V) showed more affinity than Cr(VI) for sorption sites on most materials (sorption up to >84 % on oak ash and pyritic material). The only exception was pine bark, with clearly higher Cr(VI) sorption (>90 %) for any Cr(VI)/As(V) concentration added. Regarding the displacement experiments, when As(V) was added and reached sorption equilibrium, the subsequent addition of equal Cr(VI) concentration did not cause relevant As displacement from oak ash and pyritic material, indicating strong As bindings, and/or low competitive effects. When Cr(VI) was added and reached sorption equilibrium, the subsequent addition of equal As(V) concentration caused Cr(VI) displacement from all materials except pine bark, indicating weak Cr bindings. In view of these results, oak ash and the pyritic material could be used to remove As(V) in concentrations as high as 6 mmol L(-1), even in the presence of a wide range of Cr(VI) concentrations, whereas pine bark could be used to remove Cr(VI) concentrations as high as 6 mmol L(-1). The other materials assayed (including hemp waste, studied for the first time as As(V) and Cr(VI) bio-sorbent) cannot be considered appropriate to remove As(V) and/or Cr(VI) from polluted media.

  6. Enhanced removal of Cr(VI) from aqueous solution by supported ZnO nanoparticles on biochar derived from waste water hyacinth.

    Science.gov (United States)

    Yu, Jiangdong; Jiang, Chunyan; Guan, Qingqing; Ning, Ping; Gu, Junjie; Chen, Qiuling; Zhang, Junmin; Miao, Rongrong

    2018-03-01

    Biochar derived from waste water hyacinth was prepared and modified by ZnO nanoparticles for Cr(VI) removal from aqueous solution with the aim of Cr(VI) removal and management of waste biomass. The effect of carbonization temperature (500-800 °C), ZnO content (10-50 wt%) loaded on biochar and contact time (0.17-14 h) on the Cr(VI) removal were investigated. It was found that higher than 95% removal efficiency of Cr(VI) can be achieved with the biochar loaded 30 wt% ZnO. The adsorption kinetics of the sorbent is consistent with the pseudo-second-order kinetic model and adsorption isotherm follows the Langmuir model with maximum adsorption capacity of 43.48 mg g-1 for Cr(VI). Multiple techniques such as XRD, XPS, SEM, EDX and FT-IR were performed to investigate the possible mechanisms involved in the Cr (VI) adsorption. The results show that there is precipitation between chromium ions and Zn oxide. Furthermore, the ZnO nanoparticles acts as photo-catalyst to generate photo-generated electrons to enhance the reduction of Cr(VI) to Cr(III). The as-prepared ZnO/BC possess good recyclability and the removal ratio remained at about 70% in the fifth cycle, which suggests that both contaminants removal and effective management of water hyacinth can be achieved by the approach. Copyright © 2017 Elsevier Ltd. All rights reserved.

  7. Chromium(VI) generation in vadose zone soils and alluvial sediments of the southwestern Sacramento Valley, California: a potential source of geogenic Cr(VI) to groundwater

    Science.gov (United States)

    Mills, Christopher T.; Morrison, Jean M.; Goldhaber, Martin B.; Ellefsen, Karl J.

    2011-01-01

    Concentrations of geogenic Cr(VI) in groundwater that exceed the World Health Organization’s maximum contaminant level for drinking water (50 μg L−1) occur in several locations globally. The major mechanism for mobilization of this Cr(VI) at these sites is the weathering of Cr(III) from ultramafic rocks and its subsequent oxidation on Mn oxides. This process may be occurring in the southern Sacramento Valley of California where Cr(VI) concentrations in groundwater can approach or exceed 50 μg L−1. To characterize Cr geochemistry in the area, samples from several soil auger cores (approximately 4 m deep) and drill cores (approximately 25 m deep) were analyzed for total concentrations of 44 major, minor and trace elements, Cr associated with labile Mn and Fe oxides, and Cr(VI). Total concentrations of Cr in these samples ranged from 140 to 2220 mg per kg soil. Between 9 and 70 mg per kg soil was released by selective extractions that target Fe oxides, but essentially no Cr was associated with the abundant reactive Mn oxides (up to ~1000 mg hydroxylamine-reducible Mn per kg soil was present). Both borehole magnetic susceptibility surveys performed at some of the drill core sites and relative differences between Cr released in a 4-acid digestion versus total Cr (lithium metaborate fusion digestion) suggest that the majority of total Cr in the samples is present in refractory chromite minerals transported from ultramafic exposures in the Coast Range Mountains. Chromium(VI) in the samples studied ranged from 0 to 42 μg kg−1, representing a minute fraction of total Cr. Chromium(VI) content was typically below detection in surface soils (top 10 cm) where soil organic matter was high, and increased with increasing depth in the soil auger cores as organic matter decreased. Maximum concentrations of Cr(VI) were up to 3 times greater in the deeper drill core samples than the shallow auger cores. Although Cr(VI) in these vadose zone soils and sediments was only a

  8. Can iron oxides remove Cr(VI) from drinking water at sub-ppb levels?

    Science.gov (United States)

    Kaprara, Efthymia; Simeonidis, Konstantinos; Samaras, Petros; Zouboulis, Anastasios; Mitrakas, Manassis

    2013-04-01

    Hexavalent chromium [Cr(VI)] has long been recognized as a potential carcinogen via inhalation, in contrast to trivalent chromium [Cr(III)] which is 100 times less toxic and also a necessary nutrient, essential to human glucidic metabolism. Nowadays there is an increasing concern that Cr(VI) is also carcinogenic by the oral route of exposure, while an increased number of publications indicate that Cr(VI) is a common natural pollutant. Hexavalent chromium formation is attributed to natural oxidation of Cr(III) in ultramafic derived soils and ophiolithic rocks. To verify this theory, drinking water samples were collected from targeted areas of Greece e.g. areas in which the geological background is predominated by ultramafic minerals and the water supply depends mainly on groundwater resources. Valuable guide for the samples collection was the geological map of Greece and emphasis was given to regions where the natural occurrence of Cr(VI) is thought to be more possible. A wide range of Cr concentrations (2-100 μg/L) were detected in the areas studied, with most of them ranging below the current limit of 50 μg/L, and the Cr(VI) concentration being more than 90% of the total. Since the Cr(VI) affects significant part of population worldwide, a debate was established concerning the enforcement of stringent regulation, which also demands the drinking water treatment processes re-evaluation in view of Cr(VI) removal at sub-ppb level. In this regard, adsorption has evolved as the front line of defense for chromium removal. The motivation of this work was to investigate the efficiency of iron oxides for the adsorption of Cr(VI) from drinking water and its removal at sub-ppb levels. The adsorbents examined included iron oxy-hydroxides and magnetite prepared using common low cost iron salts. Their effectiveness as Cr(VI) adsorbents was evaluated through the decrease of a Cr(VI) concentration of 100μg/L prepared in NSF water at pH 7. Preliminary batch experiments did not

  9. Efficient removal of Cr(VI) from wastewater under sunlight by Fe(II)-doped TiO{sub 2} spherical shell

    Energy Technology Data Exchange (ETDEWEB)

    Xu, S.C., E-mail: scxu@issp.ac.cn [Key Laboratory of Materials Physics, Anhui Key Laboratory of Nanomaterials and Nanotechnology, Institute of Solid State Physics, Chinese Academy of Sciences, Hefei 230031 (China); Pan, S.S.; Xu, Y.; Luo, Y.Y.; Zhang, Y.X. [Key Laboratory of Materials Physics, Anhui Key Laboratory of Nanomaterials and Nanotechnology, Institute of Solid State Physics, Chinese Academy of Sciences, Hefei 230031 (China); Li, G.H., E-mail: ghli@issp.ac.cn [Key Laboratory of Materials Physics, Anhui Key Laboratory of Nanomaterials and Nanotechnology, Institute of Solid State Physics, Chinese Academy of Sciences, Hefei 230031 (China); University of Science and Technology of China, Hefei 230026 (China)

    2015-02-11

    Graphical abstract: - Highlights: • Fe(II)/TiO{sub 2} spherical shell catalyst was synthesized by hydrothermal method. • Cr(VI) removal effectiveness reaches to 99.99% with 102.3 ppm initial content. • TiO{sub 2}, Fe(II) and Fe{sup 0} atom synergistically contribute to Cr(VI) reduction. • Bulk Fe(II) doping enhance electron transference between TiO{sub 2} and Fe(II) ions. • Special spherical shell structure enhances the utilization of sunlight. - Abstract: Fe(II)-doped TiO{sub 2} spherical shell catalyst was synthesized by one-pot hydrothermal method. The photocatalytic removal of Cr(VI) from plating wastewater under sunlight of the catalyst was demonstrated. It was found that the removal effectiveness of about 99.99% for initial Cr(VI) concentration of 102.3 ppm and 99.01% for 153.4 ppm under 3 h sunlight irradiation is realized. The Fe(II) ions serve not only as reducing agents for reducing the Cr(VI) to Cr(III) but also as an intermedium of a two-step reduction, in which the TiO{sub 2} photoreduces the Fe(II) ions to Fe atoms firstly, and then the Fe atoms reduce the Cr(VI) to Cr(III). The improved photocatalytic activity of the catalyst is considered due to the synergistic effect of a multi reducing process by Fe(II) doping. The extended optical response and effectively utilization of sunlight of the special spherical-shell-like morphology also contribute to the enhanced photocatalytic activity.

  10. Adsorption behavior of carboxylated cellulose nanocrystal—polyethyleneimine composite for removal of Cr(VI) ions

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Chao; Jin, Ru-Na; Ouyang, Xiao-kun, E-mail: xkouyang@zjou.edu.cn; Wang, Yang-Guang

    2017-06-30

    Highlights: • A carboxylated cellulose nanocrystal-polyethyleneimine composite (CCN-PEI) was prepared. • The as-prepared CCN-PEI was characterized by SEM, TEM, FT-IR, and XPS. • Results suggested that the reusable CCN-PEI could remove Cr(VI) from aqueous solutions with a high adsorption capacity. • The adsorption isotherm, thermodynamics, and kinetics of the adsorption process are also discussed. - Abstract: In this study, a composite adsorbent (CCN-PEI) composed of carboxylated cellulose nanocrystals (CCN) and polyethyleneimine (PEI) was prepared through an amidation reaction between the carboxyl groups of the CCN and the amine groups of the PEI. The adsorption performance of the CCN-PEI was tested by removing Cr(VI) ions from aqueous solutions. The physicochemical properties of the CCN and the Cr(VI) ion-loaded CCN-PEI were studied using scanning electron microscopy (SEM), transmission electron microscopy, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy. To investigate the adsorption kinetics of Cr(VI) ions onto this newly developed CCN-PEI, we performed experiments under different adsorption conditions, by varying the contact time, solution pH, initial Cr(VI) ion concentration, and adsorption temperature. The prepared CCN-PEI exhibited an encouraging uptake capacity of 358.42 mg × g{sup −1}. The adsorption process was fast: within the first 100 min, Cr(VI) ion adsorption onto the CCN-PEI was about 65%, and the adsorption equilibrium was reached within 250 min. Kinetics experiments indicated that the adsorption process could be described by a pseudo-second-order kinetic model. Furthermore, our adsorption equilibrium data fit the Langmuir isotherms well. The calculated thermodynamic parameters, such as the free energy change (ΔG = −2.93 kJ × mol{sup −1}), enthalpy change (ΔH = −5.69 kJ × mol{sup −1}), and entropy change (ΔS = −9.14 kJ × mol{sup −1}), indicate that the adsorption of Cr(VI) ions onto CCN

  11. Simultaneous removal of Cr(VI) and 4-chlorophenol through photocatalysis by a novel anatase/titanate nanosheet composite: Synergetic promotion effect and autosynchronous doping.

    Science.gov (United States)

    Liu, Wen; Sun, Weiling; Borthwick, Alistair G L; Wang, Ting; Li, Fan; Guan, Yidong

    2016-11-05

    Clean-up of wastewaters with coexisting heavy metals and organic contaminants is a huge issue worldwide. In this study, a novel anatase/titanate nanosheet composite material (labeled as TNS) synthesized through a one-step hydrothermal reaction was demonstrated to achieve the goal of simultaneous removal of Cr(VI) and 4-cholophenol (4-CP) from water. TEM and XRD analyses indicated the TNS was a nano-composite of anatase and titanate, with anatase acting as the primary photocatalysis center and titanate as the main adsorption site. Enhanced photocatalytic removal of co-existent Cr(VI) and 4-CP was observed in binary systems, with apparent rate constants (k1) for photocatalytic reactions of Cr(VI) and 4-CP about 3.1 and 2.6 times of that for single systems. In addition, over 99% of Cr(VI) and 4-CP was removed within 120min through photocatalysis by TNS at pH 7 in the binary system. Mechanisms for enhanced photocatalytic efficiency in the binary system are identified as: (1) a synergetic effect on the photo-reduction of Cr(VI) and photo-oxidation of 4-CP due to efficient separation of electron-hole pairs, and (2) autosynchronous doping because of reduced Cr(III) adsorption onto TNS. Furthermore, TNS could be efficiently reused after a simple acid-base treatment. Copyright © 2016 Elsevier B.V. All rights reserved.

  12. Cr(VI) sorption by free and immobilised chromate-reducing bacterial cells in PVA-alginate matrix: equilibrium isotherms and kinetic studies.

    Science.gov (United States)

    Rawat, Monica; Rawat, A P; Giri, Krishna; Rai, J P N

    2013-08-01

    Chromate-resistant bacterial strain isolated from the soil of tannery was studied for Cr(VI) bioaccumulation in free and immobilised cells to evaluate its applicability in chromium removal from aqueous solution. Based on the comparative analysis of the 16S rRNA gene, and phenotypic and biochemical characterization, this strain was identified as Paenibacillus xylanilyticus MR12. Mechanism of Cr adsorption was also ascertained by chemical modifications of the bacterial biomass followed by Fourier transform infrared spectroscopy analysis of the cell wall constituents. The equilibrium biosorption analysed using isotherms (Langmuir, Freundlich and Dubinin-Redushkevich) and kinetics models (pseudo-first-order, second-order and Weber-Morris) revealed that the Langmuir model best correlated to experimental data, and Weber-Morris equation well described Cr(VI) biosorption kinetics. Polyvinyl alcohol alginate immobilised cells had the highest Cr(VI) removal efficiency than that of free cells and could also be reused four times for Cr(VI) removal. Complete reduction of chromate in simulated effluent containing Cu(2+), Mg(2+), Mn(2+) and Zn(2+) by immobilised cells, demonstrated potential applications of a novel immobilised bacterial strain MR12, as a vital bioresource in Cr(VI) bioremediation technology.

  13. Biosorbent encapsulation in calcium alginate: Effects of process variables on Cr(VI) removal from solutions.

    Science.gov (United States)

    Šillerová, Hana; Komárek, Michael; Liu, Chang; Poch, Jordi; Villaescusa, Isabel

    2015-09-01

    Selected biosorbents, brewers draff and grape waste, have been encapsulated in calcium alginate beads and used for the removal of Cr(VI) from aqueous solutions. The effects of encapsulation variables, including the type of waste, the percentage of waste in the beads and the curing time of the beads in CaCl2, on the diameters of the beads and Cr(VI) sorption kinetics have been evaluated. In total, 21 different types of beads were produced. The diameters of the beads increased with increasing amounts of encapsulated biomaterial. Beads that contained grape waste were larger than those containing brewers draff. The most efficient beads for Cr(VI) removal were beads that contained 4% (w/w) of grape waste. No significant differences in the kinetics of Cr(VI) sorption were found with respect to the curing time variable in the case of grape waste calcium alginate beads. Statistical analysis confirmed that the type and percentage of waste are the critical parameters influencing the diameters of the beads and Cr(VI) removal. It was proven that the sorption efficiencies of the beads containing draff and grape waste encapsulated under the optimum conditions were much higher than the efficiencies obtained when using both wastes in their native states. Copyright © 2015 Elsevier B.V. All rights reserved.

  14. Cr(VI) Adsorption to Magnetic Iron Oxide Nanoparticle-Multi-Walled Carbon Nanotube Adsorbents.

    Science.gov (United States)

    Lee, Chang-Gu; Kim, Song-Bae

    2016-11-01

      The aim of this study was to investigate the Cr(VI) adsorption to magnetic iron oxide(MIO) nanoparticle- multi-walled carbon nanotubes (MWCNTs) in aqueous solutions using batch experiments. Results show that the maximum adsorption capacity of Cr(VI) to MIO-MWCNTs was 11.256 mg/g. Kinetic model analysis demonstrates that the pseudo-second-order model and Elovich model are suitable for describing the kinetic data. Thermodynamic analysis indicates that Cr(VI) adsorption to MIO-MWCNTs decreased with increasing temperature from 5-60 °C, indicating the spontaneous and exothermic nature of the sorption process. Equilibrium isotherm analysis demonstrates that the Redlich-Peterson model suitably describes the equilibrium data. In the pH experiments, Cr(VI) adsorption to MIO-MWCNTs decreased gradually from 5.70-2.13 mg/g with increasing pH from 3.0-7.3. Sequential extraction indicates that, among the five binding forms of Cr(VI) associated with MIO-MWCNTs, the predominant contributions are the fraction bound to Fe-Mn oxides (57.82%) and the residual (23.38%).

  15. Column study of Cr(VI) removal by cationic hydrogel for in-situ remediation of contaminated groundwater and soil.

    Science.gov (United States)

    Tang, Samuel C N; Yin, Ke; Lo, Irene M C

    2011-07-01

    Column experiments were conducted for examining the effectiveness of the cationic hydrogel on Cr(VI) removal from groundwater and soil. For in-situ groundwater remediation, the effects of background anions, humic acid (HA) and pH were studied. Cr(VI) has a higher preference for being adsorbed onto the cationic hydrogel than sulphate, bicarbonate ions and HA. However, the adsorbed HA reduced the Cr(VI) removal capacity of the cationic hydrogel, especially after regeneration of the adsorbents, probably due to the blockage of adsorption sites. The Cr(VI) removal was slightly influenced by the groundwater pH that could be attributed to Cr(VI) speciation. The 6-cycle regeneration and reusability study shows that the effectiveness of the cationic hydrogel remained almost unchanged. On average, 93% of the adsorbed Cr(VI) was recovered in each cycle and concentrated Cr(VI) solution was obtained after regeneration. For in-situ soil remediation, the flushing water pH had an insignificant effect on the release of Cr(VI) from the soils. Multiple-pulse flushing increased the removal of Cr(VI) from the soils. In contrast, more flushing water and longer operation may be required to achieve the same removal level by continuous flushing. Copyright © 2011 Elsevier B.V. All rights reserved.

  16. The applications of populus fiber in removal of Cr(VI) from aqueous solution

    Science.gov (United States)

    Li, Miaomiao; Gong, Yumei; Lyu, Aichao; Liu, Yuanfa; Zhang, Hong

    2016-10-01

    The surface modification of natural materials to be applied in removal of Cr(VI) from aqueous solutions has attracted much attention. A natural sorbent for Cr(VI) based on natural populus fibers (PF) is prepared by transforming the cyano groups (AN) in polyacrylonitriles (PAN) grafted from PF into amidoxime groups (AO), which has strong ability to attract and chelate heavy metal ions. The prepared sorbent is characterized by Fourier Transform Infrared Spectra (FT-IR), thermogravimetric analysis (TGA), solid-state nuclear magnetic resonance (13C NMR) and scanning electron microscope (SEM). As potassium dichromate solution (K2Cr2O7) is used as a target solution for detecting adsorption capacity of the sorbent, the adsorption kinetics of the sorbent for chromiun is consistent with the pseudo-second-order kinetic model by analyzing the adsorption amount as a function of the sorbent dispersed duration in solution at pH = 2. The expected adsorption mechanism is that the Cr(VI) in anionic ions Cr2O72- and HCrO4- are adsorbed through electrostatic attraction but when Cr(VI) is reduced to Cr(III) by AO, the electronegative nitrogen and oxygen in AO chelate it through coordination bond. The as-prepared PF derivant with high adsorption efficiency of chromium 180.5 mg/g (3.47 mmol/g), low cost, reusability and greenly preparation process suggests that the development of natural PF as a sorbent in removal of Cr(VI) from aqueous solutions is a destined significant approach.

  17. Effect of Cr(VI) concentration on gas and particle production during iron oxidation in aqueous solutions containing Cl- ions.

    Science.gov (United States)

    Ahn, Hyangsig; Jo, Ho Young; Ryu, Ji-Hun; Koh, Yong-Kwon

    2017-02-01

    Zero-valent iron (ZVI) is commonly used as a medium in permeable reactive barriers (PRBs) because of its high reducing ability. The generation of H2 gas in PRBs, however, can decrease the permeability of PRBs and reduce the contact area between the PRB and contaminated groundwater. This study investigated the effect of the initial Cr(VI) concentration ([Cr(VI)init]) in aqueous solutions containing Cl- ions on the generation of H2 gas. ZVI chips were reacted in reactors with 0.5-M NaCl solutions with [Cr(VI)init] ranging between 51 and 303 mg/L. The initial pH was set at 3. The oxidation of ZVI chips by Cr(VI) in aqueous solutions containing Cl- ions produced H2 gas and particles (Fe(III)-Cr(III)(oxy)hydroxides). The Cr(VI) removal from aqueous solutions increased as the [Cr(VI)init] increased, as did H2 gas generation. The positive effect of [Cr(VI)init] on H2 gas generation might be due to an increase in the redox potential gradient as [Cr(VI)init] increases. This increased gradient would enhance H+ ion penetration through the passive film (Fe(III)-Cr(III)(oxy)hydroxides), which formed on the ZVI surface, by diffusion from the solution to pits beneath the passive film.

  18. Sn(II) oxy-hydroxides as potential adsorbents for Cr(VI)-uptake from drinking water: An X-ray absorption study.

    Science.gov (United States)

    Pinakidou, Fani; Kaprara, Efthimia; Katsikini, Maria; Paloura, Eleni C; Simeonidis, Konstantinos; Mitrakas, Manassis

    2016-05-01

    The feasibility of implementing a Sn(II) oxy-hydroxide (Sn6O4(OH)4) for the reduction and adsorption of Cr(VI) in drinking water treatment was investigated using XAFS spectroscopies at the Cr-K-edge. The analysis of the Cr-K-edge XANES and EXAFS spectra verified the effective use of Sn6O4(OH)4 for successful Cr(VI) removal. Adsorption isotherms, as well as dynamic Rapid Small Scale Test (RSSCT) in NSF water matrix showed that Sn6O4(OH)4 can decrease Cr(VI) concentration below the upcoming regulation limit of 10μg/L for drinking water. Moreover, an uptake capacity of 7.2μg/mg at breakthrough concentration of 10μg/L was estimated from the RSSCT, while the residual Cr(VI) concentration ranged at sub-ppb level for a significant period of the experiment. Furthermore, no evidence for the formation of Cr(OH)3 precipitates was found. On the contrary, Cr(III)-oxyanions were chemisorbed onto SnO2, which was formed after Sn(II)-oxidation during Cr(VI)-reduction. Nevertheless, changes in the type of Cr(III)-inner sphere complexes were observed after increasing surface coverage: Cr(III)-oxyanions preferentially sorb in a geometry which combines both bidentate binuclear ((2)C) and monodentate ((1)V) geometries, at the expense of the present bidentate mononuclear ((2)E) contributions. On the other hand, the pH during sorption does not affect the adsorption mechanism of Cr(III)-species. The implementation of Sn6O4(OH)4 in water treatment technology combines the advantage of rapidly reducing a large amount of Cr(VI) due to donation of two electrons by Sn(II) and also the strong chemisorption of Cr(III) in a combination of the (2)C and (1)V configurations, which enhances the safe disposal of spent adsorbents. Copyright © 2016 Elsevier B.V. All rights reserved.

  19. Preparation and characterization of magnetic Fe3O 4/CNT nanoparticles by RPO method to enhance the efficient removal of Cr(VI).

    Science.gov (United States)

    Chen, Runhua; Chai, Liyuan; Li, Qinzhu; Shi, Yan; Wang, Yangyang; Mohammad, Ali

    2013-10-01

    This work described a novel method for the synthesis of high-ferromagnetism nanoparticles (Fe3O4/CNTs) to efficiently remove Cr(VI) from aqueous solution. The Fe3O4/carbon nanotubes (CNTs) were prepared by in situ reduction with post-oxidation method by using cheap and environmentally friendly precursor under mild condition. Magnetic hysteresis loops revealed that Fe3O4/CNTs had superior saturation magnetization (152 emu/g), enabling the highly efficient recovery of Fe3O4/CNTs from aqueous solution by magnetic separation at low magnetic field gradients. FTIR, Raman, XPS, and TEM observations were employed to characterize the physical-chemical properties of Fe3O4/CNTs, demonstrating that CNTs were successfully coated with iron oxide matrix. The adsorption equilibrium of Cr(VI) on Fe3O4/CNTs was reached within 30 min. Langmuir, Freundlich, and Dubinin-Radushkevich isotherm were chosen to analyze the equilibrium data. The results indicated that Langmuir model can well describe the equilibrium data with the maximum adsorption capacity of 47.98 mg/g at room temperature and 83.54 mg/g at 353 K. The adsorption capacity of Fe3O4/CNTs for Cr(VI) was greatly improved as compared to raw CNTs and other similar adsorbents reported. The pseudo-second-order kinetic model provided the best description of Cr(VI) adsorption on Fe3O4/CNTs. Most importantly, possible synthesis mechanism and Cr(VI) removal mechanism were explored. The results suggest that large amounts of Cr(VI) were adsorbed on Fe3O4/CNTs surface by substituting the surface position of -OH and then reducing it to Cr(OH)3 and Cr2O3.

  20. Biosorption of Cr(VI from Aqueous Solutions Using Trametes Versicolor Polyporus Fungi

    Directory of Open Access Journals (Sweden)

    M. Venkata Subbaiah

    2008-01-01

    Full Text Available Removal of chromium(VI from aqueous solution was studied using abundantly available trametes versicolor polyporus fungi as biosorbing medium under equilibrium and column flow conditions. Various sorption parameters such as contact time, effect of pH, concentration of Cr(VI and amount of biomass on the adsorption capacity of the biosorbent were studied. The equilibrium adsorption data were fitted to Freundlich and Langmuir adsorption isotherm models and the model parameters are evaluated. In addition, the data were used to predict the kinetics of adsorption. The results indicated that the adsorption of Cr(VI on fungi followed second order kinetics. The column flow adsorption data were used to predict break through curves. The fungi loaded with Cr(VI was regenerated with 0.1 M NaOH solution and the regenerated biomass was used in the subsequent adsorptiondesorption cycles. The experimental results demonstrated that the trametes versicolor polyporus fungi could be used as sorbent for immobilizing Cr(VI.

  1. Chromium(VI) reduction by catechol(amine)s results in DNA cleavage in vitro

    DEFF Research Database (Denmark)

    Pattison, D I; Davies, Michael Jonathan; Levina, A

    2001-01-01

    is reduced considerably by treatment of the Cr(VI)/catechol(amine) mixtures with catalase, which shows that the DNA damage is H(2)O(2)-dependent and that the major reactive intermediates are likely to be Cr(V)-peroxo and mixed Cr(V)-catechol-peroxo complexes, rather than Cr(V)-catechol intermediates....

  2. K4Nb6O17·4.5H2O: a novel dual functional material with quick photoreduction of Cr(VI) and high adsorptive capacity of Cr(III).

    Science.gov (United States)

    Ma, Yuli; Liu, Xiaoqing; Li, Yang; Su, Yiguo; Chai, Zhanli; Wang, Xiaojing

    2014-08-30

    A series of orthorhombic phase K4Nb6O17·4.5H2O was synthesized via a hydrothermal approach. When presented in an acidic pH range, K4Nb6O17·4.5H2O showed a strong ability in quick reduction from Cr(VI) to Cr(III). The resulted Cr(III) ions were removed by an effective adsorption through simply adjusting the solution pH from strong acidity to near neutrality, owing to the sample's unique nano-sheet structure with a wide layer spacing. The Cr(III) ions adsorbed onto samples were released again for reusing by eluting with 1molL(-1) HCl solution, and K4Nb6O17·4.5H2O regenerated by immersing in a KOH solution. The reduction efficiency of Cr(VI) was still up to 98% after irradiation for 60min, and the removal efficiency of Cr(III) ions was as high as 83% even after five cycles. Therefore, K4Nb6O17·4.5H2O is clearly demonstrated to be an excellent dual functional material with quick photoreduction of Cr(VI) and high adsorptive capacity of Cr(III). The relevant materials reported herein might be found various environment-related applications. Copyright © 2014 Elsevier B.V. All rights reserved.

  3. Magnetic vinylphenyl boronic acid microparticles for Cr(VI) adsorption: Kinetic, isotherm and thermodynamic studies

    Energy Technology Data Exchange (ETDEWEB)

    Kara, Ali, E-mail: akara@uludag.edu.tr [Uludag University, Faculty of Arts and Science, Department of Chemistry, 16059 Bursa (Turkey); Demirbel, Emel [Uludag University, Faculty of Arts and Science, Department of Chemistry, 16059 Bursa (Turkey); Tekin, Nalan [Kocaeli University, Faculty of Arts and Science, Department of Chemistry, 41380 Kocaeli (Turkey); Osman, Bilgen; Beşirli, Necati [Uludag University, Faculty of Arts and Science, Department of Chemistry, 16059 Bursa (Turkey)

    2015-04-09

    Highlights: • Cr(VI) can oxidize biological molecules and be one of the most harmful substance. • Magnetic seperation techniques are used on different applications in many fields. • Magnetic systems can be used for rapid and selective removal as a magnetic processor. • We investigate properties of both new material and other magnetic adsorbents reported in the literatures on the adsorption of Cr(VI) ions. • No researchments were reported on adsorption of Cr(VI) with magnetic vinylphenyl boronic acid microparticles. - Abstract: Magnetic vinylphenyl boronic acid microparticles, poly(ethylene glycol dimethacrylate(EG)–vinylphenyl boronic acid(VPBA)) [m-poly(EG–VPBA)], produced by suspension polymerization and characterized, was found to be an efficient solid polymer for Cr(VI) adsorption. The m-poly(EG–VPBA) microparticles were prepared by copolymerizing of ethylene glycol dimethylacrylate (EG) with 4-vinyl phenyl boronic acid (VPBA). The m-poly(EG–VPBA) microparticles were characterized by N{sub 2} adsorption/desorption isotherms, electron spin resonance (ESR), X-ray diffraction (XRD), fourier transform infrared spectroscopy (FTIR), thermal gravimetric analysis (TGA), elemental analysis, scanning electron microscope (SEM) and swelling studies. The m-poly(EG–VPBA) microparticles were used at adsorbent/Cr(VI) ion ratios. The influence of pH, Cr(VI) initial concentration, temperature of the removal process was investigated. The maximum removal of Cr(VI) was observed at pH 2. Langmuir isotherm and Dubinin–Radushkvich isotherm were found to better fit the experiment data rather than Fruendlich isotherm. The kinetics of the adsorption process of Cr(VI) on the m-poly(EG–VPBA) microparticles were investigated using the pseudo first-order, pseudo-second-order, Ritch-second-order and intraparticle diffusion models, results showed that the pseudo-second order equation model provided the best correlation with the experimental results. The thermodynamic

  4. The Effect of Phosphatation and Granulation Zeolite in the Adsorption of Cr(VI)

    OpenAIRE

    Sri Wardhani; Reno Sunarinda Endrayana; Danar Purwonugroho

    2017-01-01

    The purpose of this research to study effect of contact time on adsorption of Cr(VI) ion using Granules Alumino Silico Phosphate (GASP) and the effect of Cr (VI) concentration on adsorption capacity at GASP. The GASF synthesis process is carried out in several main stages: 1) activation of zeolite with addition of HCl, 2) zeolite phosphatation with addition of NH4H2PO4 ratio Si/P = 1/6 at 235ᴼC for 5 hours, 3) how make GASP with addition of zeolite phosphate (Alumino Silicone Phosphate) and c...

  5. Proteomic Characterization of Cr(VI) resistent Bacteria In Wastewater Effluents

    DEFF Research Database (Denmark)

    Koçberber Kılıç, nur; Kjeldal, Henrik; Lolas, Ihab Bishara Yousef

    of heavy metals were isolated by enrichment cultures from locations in Turkey. Degradation or resistance characteristics were determined by quantitative proteomics for. Membrane and cytosolic fractions were prepared, digested in gel or in solution followed by high resolution shotgun sequencing using either...... on four bacterial strains capable of tolerating extreme levels of Cr(VI) in vivo. The detailed investigation of four Cr(VI) tolerant bacterial strains also gave clear indications of novel gene products involved in the resistence mechanisms. A detailed mapping of the proteins involved in the tolerance...

  6. Adsorption behavior and mechanism of Cr(VI) using Sakura waste from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Qi, Wenfang [School of Environmental Science and Engineering, Tianjin University, Tianjin 300072 (China); Zhao, Yingxin, E-mail: yingxinzhao@tju.edu.cn [School of Environmental Science and Engineering, Tianjin University, Tianjin 300072 (China); Tianjin Engineering Center of Urban River Eco-Purification Technology, Tianjin 300072 (China); Zheng, Xinyi [School of Environmental Science and Engineering, Tianjin University, Tianjin 300072 (China); Ji, Min [School of Environmental Science and Engineering, Tianjin University, Tianjin 300072 (China); Tianjin Engineering Center of Urban River Eco-Purification Technology, Tianjin 300072 (China); Zhang, Zhenya [Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba 3058572 (Japan)

    2016-01-01

    Graphical abstract: The main chemical components of Sakura leaves are cellulose 16.6%, hemicellulose 10.4%, lignin 18.3%, ash 11.4%, and others 43.3%. The adsorption capacity of Cr(VI) onto Sakura leaves can achieve 435.25 mg g{sup −1}, much higher than other similar agroforestry wastes. - Highlights: • Sakura leaves were prepared to remove Cr(VI) from aqueous solution. • The maximum adsorption capacity of Cr(VI) reached 435.25 mg g{sup −1}. • Cr(VI) adsorption fitted pseudo-second-order kinetic model. • Isotherm models indicated Cr(VI) adsorption occurred on a monolayer surface. • The influence order of coexisting ions followed PO{sub 4}{sup 3−} > SO{sub 4}{sup 2−} > Cl{sup −}. - Abstract: A forestall waste, Sakura leave, has been studied for the adsorption of Cr(VI) from aqueous solution. The materials before and after adsorption were characterized by X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR). To investigate the adsorption performance of Sakura waste, batch experiments were conducted under different adsorbent dosage, contact time, initial concentration of Cr(VI), and co-existing ions. Results showed the data fitted pseudo-second-order better than pseudo-first-order kinetic model. Equilibrium data was analyzed with Langmuir, Freundlich and Redlich–Peterson isotherm models at temperature ranges from 25 °C to 45 °C. The maximum adsorption capacity from the Langmuir model was 435.25 mg g{sup −1} at pH 1.0. The presence of Cl{sup −}, SO{sub 4}{sup 2−} and PO{sub 4}{sup 3−} would lead to an obvious negative effect on Cr(VI) adsorption, and their influence order follows PO{sub 4}{sup 3−} > SO{sub 4}{sup 2−} > Cl{sup −}. The study developed a new way to reutilize wastes and showed a great potential for resource recycling.

  7. Nanoscale zero-valent iron supported by biochars produced at different temperatures: Synthesis mechanism and effect on Cr(VI) removal.

    Science.gov (United States)

    Qian, Linbo; Zhang, Wenying; Yan, Jingchun; Han, Lu; Chen, Yun; Ouyang, Da; Chen, Mengfang

    2017-04-01

    Biochar-supported nanoscale zero-valent iron (nZVI) produced under different temperatures was studied to evaluate the effect of the nZVI-biochar composite on the removal of hexavalent chromium (Cr(VI)) in solution. The structure of biochar-supported nZVI and its roles in Cr(VI) removal were investigated by X-Ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and batch experiments. The XRD revealed that the removal rate of Cr(VI) for the nZVI supported by rice straw pyrolyzed at 400 °C (RS400) was much greater than that for other supporting biochar, and the FTIR further indicated that the carboxyl groups and silicon mineral within the biochar served as dual support sites for nZVI. NZVI-RS400 exhibited the highest removal amount of Cr(VI) at approximately 40.0 mg/g under an initial pH of 4.0, possibly due to both the reduction and adsorption processes. Therefore, the RS400-supported nanoscale zero-valent iron could be a preferable material for Cr(VI)-contaminated groundwater. Copyright © 2016. Published by Elsevier Ltd.

  8. Biological detoxification of Cr(VI) using wood-husk immobilized Acinetobacter haemolyticus

    Energy Technology Data Exchange (ETDEWEB)

    Zakaria, Zainul Akmar; Zakaria, Zainoha [Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, 81310 Skudai, Johor (Malaysia); Surif, Salmijah [Department of Environmental Sciences, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor (Malaysia); Ahmad, Wan Azlina [Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, 81310 Skudai, Johor (Malaysia)], E-mail: azlina@kimia.fs.utm.my

    2007-09-05

    Acinetobacter haemolyticus, a Gram-negative aerobic locally isolated bacterium, immobilized on wood-husk showed the ability to detoxify Cr(VI) to Cr(III). Wood-husk, a natural cellulose-based support material, packed in an upward-flow column was used as support material for bacterial attachment. Around 97% of the Cr(VI) in wastewater containing 15 mg L{sup -1} of Cr(VI) was reduced at a flow rate of 8.0 mL min{sup -1}. The wastewater containing Cr(VI) was added with liquid pineapple wastewater as nutrient source for the bacteria. Electron microscopic examinations of the wood-husk after 42 days of column operation showed gradual colonization of the wood-husk by bacterial biofilm. The use of 0.1% (v/v) formaldehyde as a disinfecting agent inhibited growth of bacteria present in the final wastewater discharge. This finding is important in view of the ethical code regarding possible introduction of exogenous bacterial species into the environment.

  9. Addition of DNA to Cr(VI) and cytochrome b5 containing proteoliposomes leads to generation of DNA strand breaks and Cr(III) complexes.

    Science.gov (United States)

    Borthiry, Griselda R; Antholine, William E; Myers, Judith M; Myers, Charles R

    2008-08-01

    Chromium (Cr) is a cytotoxic metal that can be associated with a variety of types of DNA damage, including Cr-DNA adducts and strand breaks. Prior studies with purified human cytochrome b(5) and NADPH:P450 reductase in reconstituted proteoliposomes (PLs) demonstrated rapid reduction of Cr(VI) (hexavalent chromium, as CrO(4)(2-), and the generation of Cr(V), superoxide (O(2)(*-)), and hydroxyl radical (HO(*)). Studies reported here examined the potential for the species produced by this system to interact with DNA. Strand breaks of purified plasmid DNA increased over time aerobically, but were not observed in the absence of O(2). Cr(V) is formed under both conditions, so the breaks are not mediated directly by Cr(V). The aerobic strand breaks were significantly prevented by catalase and EtOH, but not by the metal chelator diethylenetriaminepentaacetic acid (DTPA), suggesting that they are largely due to HO(*) from Cr-mediated redox cycling. EPR was used to assess the formation of Cr-DNA complexes. Following a 10-min incubation of PLs, CrO(4)(2-), and plasmid DNA, intense EPR signals at g=5.7 and g=5.0 were observed. These signals are attributed to specific Cr(III) complexes with large zero field splitting (ZFS). Without DNA, the signals in the g=5 region were weak. The large ZFS signals were not seen, when Cr(III)Cl(3) was incubated with DNA, suggesting that the Cr(III)-DNA interactions are different when generated by the PLs. After 24 h, a broad signal at g=2 is attributed to Cr(III) complexes with a small ZFS. This g=2 signal was observed without DNA, but it was different from that seen with plasmid. It is concluded that EPR can detect specific Cr(III) complexes that depend on the presence of plasmid DNA and the manner in which the Cr(III) is formed.

  10. Sn(II) oxy-hydroxides as potential adsorbents for Cr(VI)-uptake from drinking water: An X-ray absorption study

    Energy Technology Data Exchange (ETDEWEB)

    Pinakidou, Fani; Kaprara, Efthimia [Aristotle University of Thessaloniki, School of Chemical Engineering, Analytical Chemistry Laboratory, 54124 Thessaloniki (Greece); Katsikini, Maria; Paloura, Eleni C.; Simeonidis, Konstantinos [Aristotle University of Thessaloniki, School of Physics, Department of Solid State Physics, 54124 Thessaloniki (Greece); Mitrakas, Manassis, E-mail: manasis@eng.auth.gr [Aristotle University of Thessaloniki, School of Chemical Engineering, Analytical Chemistry Laboratory, 54124 Thessaloniki (Greece)

    2016-05-01

    The feasibility of implementing a Sn(II) oxy-hydroxide (Sn{sub 6}O{sub 4}(OH){sub 4}) for the reduction and adsorption of Cr(VI) in drinking water treatment was investigated using XAFS spectroscopies at the Cr-K-edge. The analysis of the Cr-K-edge XANES and EXAFS spectra verified the effective use of Sn{sub 6}O{sub 4}(OH){sub 4} for successful Cr(VI) removal. Adsorption isotherms, as well as dynamic Rapid Small Scale Test (RSSCT) in NSF water matrix showed that Sn{sub 6}O{sub 4}(OH){sub 4} can decrease Cr(VI) concentration below the upcoming regulation limit of 10 μg/L for drinking water. Moreover, an uptake capacity of 7.2 μg/mg at breakthrough concentration of 10 μg/L was estimated from the RSSCT, while the residual Cr(VI) concentration ranged at sub-ppb level for a significant period of the experiment. Furthermore, no evidence for the formation of Cr(OH){sub 3} precipitates was found. On the contrary, Cr(III)-oxyanions were chemisorbed onto SnO{sub 2}, which was formed after Sn(II)-oxidation during Cr(VI)-reduction. Nevertheless, changes in the type of Cr(III)-inner sphere complexes were observed after increasing surface coverage: Cr(III)-oxyanions preferentially sorb in a geometry which combines both bidentate binuclear ({sup 2}C) and monodentate ({sup 1}V) geometries, at the expense of the present bidentate mononuclear ({sup 2}E) contributions. On the other hand, the pH during sorption does not affect the adsorption mechanism of Cr(III)-species. The implementation of Sn{sub 6}O{sub 4}(OH){sub 4} in water treatment technology combines the advantage of rapidly reducing a large amount of Cr(VI) due to donation of two electrons by Sn(II) and also the strong chemisorption of Cr(III) in a combination of the {sup 2}C and {sup 1}V configurations, which enhances the safe disposal of spent adsorbents. - Highlights: • Effective Cr(VI) removal from drinking water by Sn{sub 6}O{sub 4}(OH){sub 4} • Sn{sub 6}O{sub 4}(OH){sub 4} transformation to SnO{sub 2} after Cr(VI

  11. Modelling of biological Cr(VI) removal in draw-fill reactors using microorganisms in suspended and attached growth systems.

    Science.gov (United States)

    Tekerlekopoulou, Athanasia G; Tsiflikiotou, Maria; Akritidou, Lydia; Viennas, Anastasios; Tsiamis, George; Pavlou, Stavros; Bourtzis, Kostas; Vayenas, Dimitris V

    2013-02-01

    The kinetics of hexavalent chromium bio-reduction in draw-fill suspended and attached growth reactors was examined using sugar as substrate and indigenous microorganisms from the industrial sludge of the Hellenic Aerospace Industry. Initially, experiments in suspended growth batch reactors for Cr (VI) concentrations of 1.4-110 mg/l were carried out, to extensively study the behaviour of a mixed culture. The maximum Cr(VI) reduction rate of 2 mg/l h was achieved for initial concentration 12.85 mg/l with biomass production rate 4.1 mg biomass/l h. Analysis of the microbial structure in the batch reactor culture indicated that the dominant bacterial communities were constituted by bacterial members of Raoultella sp., Citrobacter sp., Klebsiella sp., Salmonella sp., Achromobacter sp. and Kerstersia sp. while the dominant fungal strain was that of Pichia jadinii. Experiments using the same mixed culture were also carried out in packed-bed reactors with plastic support media. High removal rates were achieved (2.0 mg/l h) even in high initial concentrations (109 mg/l). A combination of the model of Tsao and Hanson for growth enhancement and that of Aiba and Shoda for growth inhibition was used in order to describe and predict the process of Cr(VI) bio-reduction in suspended growth and packed-bed reactors. Kinetic constants of the equation obtained from both batch (or draw-fill) culture experiments. In the draw-fill experiments at the packed-bed reactor, hexavalent chromium inhibitory effects were minimized increasing the inhibitory constant value K(i)' at 148.5 mg/l, compared to suspended growth experiments which was K(i) = 8.219 mg/l. The model adequately predicts hexavalent chromium reduction in both batch reactors for all initial concentrations tested. Copyright © 2012 Elsevier Ltd. All rights reserved.

  12. Recyclable magnetic photocatalysts of Fe{sup 2+}/TiO{sub 2} hierarchical architecture with effective removal of Cr(VI) under UV light from water

    Energy Technology Data Exchange (ETDEWEB)

    Xu, S.C.; Zhang, Y.X.; Pan, S.S.; Ding, H.L. [Key Laboratory of Materials Physics, Anhui Key Lab of Nanomaterials and Nanostructure, Institute of Solid State Physics, Chinese Academy of Sciences, Hefei 230031 (China); Li, G.H., E-mail: ghli@issp.ac.cn [Key Laboratory of Materials Physics, Anhui Key Lab of Nanomaterials and Nanostructure, Institute of Solid State Physics, Chinese Academy of Sciences, Hefei 230031 (China)

    2011-11-30

    Highlights: Black-Right-Pointing-Pointer Fe{sup 2+}/TiO{sub 2} catalyst has a three-level hierarchical architecture. Black-Right-Pointing-Pointer With a removal effectiveness of 99.3% at Cr(VI) concentration of 10 mg L{sup -1}. Black-Right-Pointing-Pointer Two-step reduction: TiO{sub 2} photoreduces Fe{sup 2+} to Fe and Fe reduces Cr(VI) to Cr(III). Black-Right-Pointing-Pointer Hierarchical architecture serves as both photocatalytic reactor and absorbent. Black-Right-Pointing-Pointer Fe{sup 2+}/TiO{sub 2} catalyst can be magnetically separated from wastewater and recycled. - Abstract: We report the synthesis and photocatalytic removal of Cr(VI) from water of hierarchical micro/nanostructured Fe{sup 2+}/TiO{sub 2} tubes. The TiO{sub 2} tubes fabricated by a facile solvothermal approach show a three-level hierarchical architecture assembled from dense nanosheets nearly vertically standing on the surface of TiO{sub 2} microtube. The nanosheets with a thickness of about 20 nm are composed of numerous TiO{sub 2} nanocrystals with size in the range of 15-20 nm. Ferrous ions are doped into the hierarchical architecture by a reduction route. The Fe{sup 2+}/TiO{sub 2} catalyst demonstrates an effective removal of Cr(VI) from water under UV light and the removal effectiveness reaches 99.3% at the initial Cr(VI) concentration of 10 mg L{sup -1}. The ferrous ion in the catalyst serves not as the photo-electron trap but as an intermedium of a two-step reduction. The TiO{sub 2} photoreduces the Fe{sup 2+} ions to Fe atoms firstly, then the Fe atoms reduce the Cr(VI) to Cr(III), and the later is removed by adsorption. The hierarchical architecture of the catalyst serves as a reactor for the photocatalytic reaction of Cr(VI) ions and an effective absorbent for the removal of Cr(III) ions. The catalyst can be easily magnetically separated from the wastewater after photocatalytic reaction and recycled after acid treatment.

  13. Enhanced photocatalytic activity of chromium(VI) reduction and EDTA oxidization by photoelectrocatalysis combining cationic exchange membrane processes

    Energy Technology Data Exchange (ETDEWEB)

    Hsu, Hung-Te, E-mail: der11065@hotmail.com [Institute of Environmental Engineering and Management, National Taipei University of Technology, No. 1, Sec. 3, Chung-Hsiao E. Rd., Taipei 106, Taiwan (China); Chen, Shiao-Shing, E-mail: f10919@ntut.edu.tw [Institute of Environmental Engineering and Management, National Taipei University of Technology, No. 1, Sec. 3, Chung-Hsiao E. Rd., Taipei 106, Taiwan (China); Tang, Yi-Fang, E-mail: sweet39005@hotmail.com [Institute of Environmental Engineering and Management, National Taipei University of Technology, No. 1, Sec. 3, Chung-Hsiao E. Rd., Taipei 106, Taiwan (China); Hsi, Hsing-Cheng, E-mail: hchsi@ntut.edu.tw [Institute of Environmental Engineering and Management, National Taipei University of Technology, No. 1, Sec. 3, Chung-Hsiao E. Rd., Taipei 106, Taiwan (China)

    2013-03-15

    Highlights: ► Chromium(VI) reduction and EDTA oxidization were conducted by photoelectrocatalysis. ► Apply the concept of cationic exchange membrane to enhance the conversion efficiency. ► The optimum TiO{sub 2} loading of 1 g/L was observed at acidic pH with current density 4 mA/cm{sup 2}. ► Transformation pathway of EDTA was determined from analyzed byproducts and molecular orbital package analysis. -- Abstract: A novel technology of photoelectrocatalysis (PEC) combining with cationic exchange membrane (CEM) was proposed for simultaneous reduction of chromium(VI) and oxidization of EDTA. The application of CEM was used to enhance the efficiency for prevention of the re-oxidation of reduced chromium with the electron–hole pairs. In this study, effects of current density, pH, TiO{sub 2} dosage, hydraulic retention time (HRT), light intensity and EDTA/Cr(VI) molar ratio were all investigated. The results showed that the optimum conversion efficiency occurred at 4 mA/cm{sup 2} with the presence of CEM. Higher conversion efficiencies were observed at lower pH due to the electrostatic attractions between positive charged Ti-OH{sub 2}{sup +}, and negatively charged Cr(VI) and EDTA. The optimum TiO{sub 2} loading of 1 g/L was depended mainly on the acidic pH range, especially at higher HRT and irradiation intensity. In addition, higher EDTA/Cr(VI) molar ratio enhanced the reduction efficiency of Cr(VI), indicating EDTA plays the role of hole scavenger in this system. Moreover, incomplete EDTA decomposition contributes to the occurrence of intermediates, including nitrilotriacetic acid, iminodiacetic acid, glycine, oxamic acid, lyoxylic acid, oxalic acid, acetic acid and formic acid, as identified by GC/MS. Consequently, transformation pathway was determined from these analyzed byproducts and molecular orbital package analysis.

  14. Dual Mechanism Conceptual Model for Cr Isotope Fractionation during Reduction by Zerovalent Iron under Saturated Flow Conditions.

    Science.gov (United States)

    Jamieson-Hanes, Julia H; Amos, Richard T; Blowes, David W; Ptacek, Carol J

    2015-05-05

    Chromium isotope analysis is rapidly becoming a valuable complementary tool for tracking Cr(VI) treatment in groundwater. Evaluation of various treatment materials has demonstrated that the degree of isotope fractionation is a function of the reaction mechanism, where reduction of Cr(VI) to Cr(III) induces the largest fractionation. However, it has also been observed that uniform flow conditions can contribute complexity to isotope measurements. Here, laboratory batch and column experiments were conducted to assess Cr isotope fractionation during Cr(VI) reduction by zerovalent iron under both static and saturated flow conditions. Isotope measurements were accompanied by traditional aqueous geochemical measurements (pH, Eh, concentrations) and solid-phase analysis by scanning electron microscopy and X-ray absorption spectroscopy. Increasing δ(53)Cr values were associated with decreasing Cr(VI) concentrations, which indicates reduction; solid-phase analysis showed an accumulation of Cr(III) on the iron. Reactive transport modeling implemented a dual mechanism approach to simulate the fractionation observed in the experiments. The faster heterogeneous reaction pathway was associated with minimal fractionation (ε=-0.2‰), while the slower homogeneous pathway exhibited a greater degree of fractionation (ε=-0.9‰ for the batch experiment, and ε=-1.5‰ for the column experiment).

  15. Sensitization of CdS nanoparticles onto reduced graphene oxide (RGO) fabricated by chemical bath deposition method for effective removal of Cr(VI)

    Energy Technology Data Exchange (ETDEWEB)

    Pawar, Rajendra C.; Lee, Caroline Sunyong, E-mail: sunyong523@gmail.com

    2013-09-16

    RGO (Reduced Graphene Oxide)–CdS composites were successfully synthesized by chemical bath deposition (CBD) method onto soda lime glass substrate at low temperature (70 °C). Their structural, optical and morphological properties were studied using X-ray diffraction, UV–Vis spectrophotometer, Raman spectroscopy, Brunauer–Emmett–Teller, Field emission scanning electron microscope and transmission electron microscope. It is clearly seen that spherically shaped CdS nanoparticles with an average diameter 30 nm are uniformly coated over the entire graphene sheet. Further, synthesized CdS nanoparticles and RGO–CdS nanocomposites were investigated for the reduction of Cr(VI) under visible light. The photocatalytic results show that photodegradation rate of RGO–CdS composites is two times higher than that of CdS nanoparticles toward reduction of Cr(VI). The improved photocatalytic performance by combining RGO with CdS nanoparticles, is attributed to its increased specific surface area (47.44 m{sup 2} g{sup −1}), efficient transportation of photoelectrons and improved absorbance of CdS nanoparticles. Therefore, it was found that RGO in RGO–CdS composites makes a significant impact on photocatalytic activity toward reduction of Cr(VI), making an excellent candidate for water refiner. - Graphical abstract: Display Omitted - Highlights: • Chemical bath deposition was used to deposit CdS nanoparticles over graphene sheets. • RGO/CdS shows effective photocatalytic reduction of Cr(VI) under visible light. • High photocurrent of RGO/CdS proved reduction in recombination due to graphene. • High specific surface area (47.44 m{sup 2} g{sup −1}) of RGO/CdS improves Cr(VI) adsorption.

  16. Photo-Catalytic Activity of ZnO Supported on H-ZSM-5 Zeolite to Reduce Cr(VI from Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Haghighi M. MSc,

    2015-12-01

    Full Text Available Aims The application of photocatalytic processes to remove heavy metals in aqueous solutions and industrial wastewater are regarded as extremely effective, clean and without producing waste methods. The goal of the present study was to investigate the photocatalytic activity of ZnO based on H-ZSM-5 zeolite support. Materials & Methods ZnO/H-ZSM-5 composite synthesized by impregnation method successfully, and photo-reduction of Cr(VI was investigated via this composite in present of UV light irradiation. The prepared composite was characterized by X-ray Diffraction (XRD and Field Emission Scanning Electron Microscopy (FESEM. Data was analyzed by repeated measurement statistical test. Findings ZnO/H-ZSM-5 (79.5% had better removal photo-reduction activity than pure H-ZSM-5 (8.7%; p=0.003 zeolite and ZnO (58.8%; p=0.003. The initial concentration of Cr(VI was a highly influential factor in photo-reduction of Cr(VI; In the way that when the initial concentration increased from 10 to 40mg/l, the photo-reduction percentage decreased from 92.5 to 57.7% in constant operational conditions (p=0.001. Conclusion ZnO/H-ZSM-5 composite has higher removal photo-catalytic activity than pure ZnO and HZSM-5 zeolite. Photo-reduction of Cr(VI by ZnO/H-ZSM-5 composite is an efficient technology for the treatment of water and wastewater containing high concentration of Cr(VI.

  17. STUDY ON SENSITIZATION OF FULVIC ACID ON PHOTOREDUCTION OF Cr(VI TO Cr(III BY TiO2 PHOTOCATALYST

    Directory of Open Access Journals (Sweden)

    Uripto Trisno Santoso

    2010-06-01

    Full Text Available Sensitization of fulvic acid (FA on photoreduction of Cr(VI to Cr(III by TiO2 photocatalyst has been studied. Parameters influencing the sensitization, i.e., pH of medium, as well as FA concentrations, TiO2 concentrations and initial Cr(VI concentrations were critically evaluated. Extraction of FA from peat soil sampled in Gambut, South Kalimantan, Indonesia, was performed using Amberlite XAD-7 resin. The FA extract then was purified by cation exchange method using Amberlite IRA-120 resin. The TiO2 produced by Merck was used as semiconducting photocatalyst and two 30-W UV lamps (Philips® model TUV were used as photon source. The results showed that presence of FA on TiO2 suspensions could sensitize the photoreduction of Cr(VI, enhancing of the amount of reduced Cr(VI more significantly than the sensitization by humic acid. The effectiveness of this sensitization increased with increasing initial concentrations of FA, TiO2, or Cr(VI until certain concentration, but no further improvement can be observed in excess FA, TiO2, or Cr(VI concentrations. On the contrary, the effectiveness of this sensitization decreased with increasing of the medium pH.   Keywords: sensitization, fulvic acid, Cr(VI, photoreduction, TiO2.

  18. Dispersion-free solvent extraction of Cr(VI) from acidic solutions using hollow fiber contactor.

    Science.gov (United States)

    Alguacil, Francisco J; Alonso, Manuel; Lopez, Félix A; Lopez-Delgado, Aurora; Padilla, Isabel

    2009-10-15

    The use of dispersión-free solvent extraction, through microporous hydrophobic membrane has been investigated. The hollow fiber contactor, with surface area of 1.4 m2 was used to extract Cr(VI) (0.005-0.12 g/L from aqueous sulphuric acidic media (pH 2.5-4.2 +/- 0.05). Several parameters such as extractant concentration, feed acidity and metal concentration in the initial aqueous solution were investigated. Results revealed that 15% v/v Cyanex 923 in Exxsol D-100 as organic phase and feed in the 2.5 pH range, gave optimum extraction (exceeding 95%) of Cr(VI) and it was possible to strip using 10 g/L hydrazine sulfate (also with recoveries exceeding 95%). In this step, Cr(VI) is immediately reduced to the less hazardous Cr(III) state. Results also showed that under the various experimental conditions, chromium(VI) extraction was rate-controlled by the interfacial reaction on the membrane surface. Typical overall mass transfer coefficients values are 4.2 x 10(-5) and 3.6 x 10(-6) cm/s for extraction and stripping operations, respectively.

  19. Cr(VI) generation during sample preparation of solid samples – A ...

    African Journals Online (AJOL)

    Cr(VI) generation during sample preparation of solid samples – A chromite ore case study. R.I Glastonbury, W van der Merwe, J.P Beukes, P.G van Zyl, G Lachmann, C.J.H Steenkamp, N.F Dawson, M.H Stewart ...

  20. Cr(VI)-free pre-treatments for adhesive bonding of aerospace aluminium alloys

    NARCIS (Netherlands)

    Abrahami, S.T.

    2016-01-01

    For more than six decades, chromic acid anodizing (CAA) has been the central process in the surface pre-treatment of aluminium for adhesively bonded aircraft structures in Europe. Unfortunately, this electrolyte contains hexavalent chromium (Cr(VI)), a compound known for its toxicity and

  1. The surface characteristics of hyperbranched polyamide modified corncob and its adsorption property for Cr(VI)

    Science.gov (United States)

    Lin, Hai; Han, Shaoke; Dong, Yingbo; He, Yinhai

    2017-08-01

    A low-cost anion adsorbent for Cr(VI) effectively removing was synthesized by hyperbranched polyamide modified corncob (HPMC). Samples were characterized by Brunauer-Emmett-Teller (BET) surface area analysis, field-emission scanning electron microscopy (FE-SEM) with energy-dispersive X-ray spectroscopy, Fourier transform infrared (FTIR) and zeta potential analysis. Kinetics, isotherms and thermodynamics studies of HPMC for Cr(VI) adsorption were investigated in batch static experiments, in the temperature range of 25-45 °C, pH = 2.0. Results showed that the adsorption was rapid and stable, with the uptake capacity higher than 80% after 30 min. Adsorption behavior and rate-controlling mechanisms were analyzed using three kinetic models (pseudo-first order, pseudo-second order, intra-particle kinetic model). Kinetic studies showed that the adsorption of HPMC to Cr(VI) relied the pseudo-second-order model, and controlled both by the intra-particle diffusion and film diffusion. Equilibrium data was tested by Langmuir and Freundlich adsorption isotherm models. Langmuir model was more suitable to indicate a homogeneous distribution of active sites on HPMC and monolayer adsorption. The maximum adsorption capacity from the Langmuir model, qmax, was 131.6 mg/g at pH 2.0 and 45 °C for HPMC. Thermodynamic parameters revealed spontaneous and endothermic nature of the Cr(VI) adsorption onto HPMC.

  2. Studies on Cr(VI) removal from aqueous solutions by nanotitania ...

    Indian Academy of Sciences (India)

    The current study deals with Cr(VI) removal by nanotitania under fluorescent light and dark conditions. The equilibrium removal capacities, ... both the conditions, the equilibrium removal data fitted well with the Langmuir isotherm model. ... state posing serious threats to the human being. Hexavalent chromium has proved to ...

  3. Polypyrrole-coated halloysite nanotube clay nanocomposite: synthesis, characterization and Cr(VI) adsorption behaviour

    CSIR Research Space (South Africa)

    Ballav, N

    2014-12-01

    Full Text Available A polypyrrole-coated halloysite nanotube nanocomposite (PPy-HNTs NC) was prepared via in situ polymerization of pyrrole (Py) in the dispersion of HNTs and assessed for the removal of toxic Cr(VI) from aqueous solutions. ATR-FTIR and XRD results...

  4. Cr(VI) and lindane removal by Streptomyces M7 is improved by maize root exudates.

    Science.gov (United States)

    Simon Sola, María Z; Pérez Visñuk, Daiana; Benimeli, Claudia S; Polti, Marta Alejandra; Alvarez, Analia

    2017-09-21

    Environmental mixed pollution by both organic and inorganic compounds are detected worldwide. Phytoremediation techniques have been proposed as ecofriendly methods for cleaning up polluted sites. Several studies have demonstrated enhanced dissipation of contaminants at the root-soil interface through an increase in microbial activity caused by the release of plant root exudates (REs). The aim of this study was to evaluate the effectiveness for Cr(VI) and lindane removal by Streptomyces M7 cultured in a co-contaminated system in presence of maize REs. Our results showed when REs were added to the contaminated minimal medium (MM) as the only carbon source, microbial removal of Cr(VI) and lindane increased significantly in comparison to contaminant removal obtained in MM with glucose 1 g L(-1) . The maximum removal of 91% of lindane and 49.5% of Cr(VI) were obtained in the co-contaminated system. Moreover, Streptomyces M7 showed plant growth promoting traits which could improve plant performance in contaminated soils. The results presented in this study provide evidence that maize REs improved growth of Streptomyces M7 when REs were used as a carbon source in comparison to glucose. Consequently, lindane and Cr(VI) removal was considerably enhanced making evident the phytoremediation potential of the actinobacteria-plant partnership. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  5. Application of plasma electrolysis method for simultaneous phenol and Cr(VI) wastewater degradation using Na2SO4 electrolyte

    Science.gov (United States)

    Harianti, Aulia Rahmi; Saksono, Nelson

    2017-11-01

    Phenol and Cr (VI) are two types of wastewater known as dangerous and difficult to degrade. Through this study, phenol and Cr (VI) metal wastewater were degraded simultaneously using plasma electrolysis method by reactive species, •OH and H•. The variation of anode depth and position of plasma formation as independent variables correlated with yield of hydroxyl radical, percentage of phenol and Cr (VI) degradation, and specific energy. Within 30 minutes, phenol was degraded to 98.4% and Cr (VI) was degraded to 93.35% with 171.05 kJ/mmol in specific energy, and 174.53 ppm in COD. The optimum condition was obtained in anodic plasma and 1.5 cm in anode depth. The highest degradation percentage of phenol and Cr (VI) were 99.79% and 97.33% achieved during 180 minutes of plasma electrolysis process.

  6. Proteomic and enzymatic response under Cr(VI) overload in yeast isolated from textile-dye industry effluent.

    Science.gov (United States)

    Irazusta, Verónica; Bernal, Anahí Romina; Estévez, María Cristina; de Figueroa, Lucía I C

    2018-02-01

    Cyberlindnera jadinii M9 and Wickerhamomyces anomalus M10 isolated from textile-dye liquid effluents has shown capacity for chromium detoxification via Cr(VI) biological reduction. The aim of the study was to evaluate the effect of hexavalent chromium on synthesis of novel and/or specific proteins involved in chromium tolerance and reduction in response to chromium overload in two indigenous yeasts. A study was carried out following a proteomic approach with W. anomalus M10 and Cy. jadinii M9 strains. For this, proteins extracts belonging to total cell extracts, membranes and mitochondria were analyzed. When Cr(VI) was added to culture medium there was an over-synthesis of 39 proteins involved in different metabolic pathways. In both strains, chromium supplementation changed protein biosynthesis by upregulating proteins involved in stress response, methionine metabolism, energy production, protein degradation and novel oxide-reductase enzymes. Moreover, we observed that Cy. jadinii M9 and W. anomalus M10 displayed ability to activate superoxide dismutase, catalase and chromate reductase activity. Two enzymes from the total cell extracts, type II nitroreductase (Frm2) and flavoprotein wrbA (Ycp4), were identified as possibly responsible for inducing crude chromate-reductase activity in cytoplasm of W. anomalus M10 under chromium overload. In Cy.jadinii M9, mitochondrial Ferredoxine-NADP reductase (Yah1) and membrane FAD flavoprotein (Lpd1) were identified as probably involved in Cr(VI) reduction. To our knowledge, this is the first study proposing chromate reductase activity of these four enzymes in yeast and reporting a relationship between protein synthesis, enzymatic response and chromium biospeciation in Cy. jadinii and W. anomalus. Copyright © 2017 Elsevier Inc. All rights reserved.

  7. Microbial conversion of Cr (VI) in to Cr (III) in industrial effluent ...

    African Journals Online (AJOL)

    Bacterial strains (CrT-11, CrT-12, Bravibacterium sp. CrT-13, CrT-14) were isolated from the effluents of tanneries. All strains could resist very high concentration of K2CrO4 that is up to 40 mg ml-1 on nutrient agar and 25 mg ml-1 in nutrient broth. They have wide pH (5 to 9) and temperature (24 to 42˚C) growth range.

  8. Cr(VI) and conductivity as Indicators of surface water pollution from ferrochrome production in South Africa: four case studies

    OpenAIRE

    Loock-Hattingh, M.M.; Beukes, J. P.; van Zyl, P. G.; L.R. Tiedt

    2015-01-01

    South Africa is one of the largest ferrochromium (FeCr) producers. Most FeCr is exported to developed countries. Therefore the impact of this industry is of national and international importance. Cr(VI) and conductivity of surface water in four case study areas, near five FeCr smelters were monitored for approximately 1 year. Results indicated that FeCr production in three case study areas had a negative influence on the Cr(VI) concentration and/or the conductivity of surface w...

  9. Micro-electrolysis of Cr (VI) in the nanoscale zero-valent iron loaded activated carbon.

    Science.gov (United States)

    Wu, Limei; Liao, Libing; Lv, Guocheng; Qin, Faxiang; He, Yujuan; Wang, Xiaoyu

    2013-06-15

    In this paper we prepared a novel material of activated carbon/nanoscale zero-valent iron (C-Fe(0)) composite. The C-Fe(0) was proved to possess large specific surface area and outstanding reducibility that result in the rapid and stable reaction with Cr (VI). The prepared composite has been examined in detail in terms of the influence of solution pH, concentration and reaction time in the Cr (VI) removal experiments. The results showed that the C-Fe(0) formed a micro-electrolysis which dominated the reaction rate. The Micro-electrolysis reaches equilibrium is ten minutes. Its reaction rate is ten times higher than that of traditional adsorption reaction, and the removal rate of Cr reaches up to 99.5%. By analyzing the obtained profiles from the cyclic voltammetry, PXRD and XPS, we demonstrate that the Cr (VI) is reduced to insoluble Cr (III) compound in the reaction. Copyright © 2013 Elsevier B.V. All rights reserved.

  10. Chromium Biosorption from Cr(VI) Aqueous Solutions by Cupressus lusitanica Bark: Kinetics, Equilibrium and Thermodynamic Studies.

    Science.gov (United States)

    Netzahuatl-Muñoz, Alma Rosa; Cristiani-Urbina, María del Carmen; Cristiani-Urbina, Eliseo

    2015-01-01

    The present study investigated the kinetics, equilibrium and thermodynamics of chromium (Cr) ion biosorption from Cr(VI) aqueous solutions by Cupressus lusitanica bark (CLB). CLB total Cr biosorption capacity strongly depended on operating variables such as initial Cr(VI) concentration and contact time: as these variables rose, total Cr biosorption capacity increased significantly. Total Cr biosorption rate also increased with rising solution temperature. The pseudo-second-order model described the total Cr biosorption kinetic data best. Langmuir´s model fitted the experimental equilibrium biosorption data of total Cr best and predicted a maximum total Cr biosorption capacity of 305.4 mg g(-1). Total Cr biosorption by CLB is an endothermic and non-spontaneous process as indicated by the thermodynamic parameters. Results from the present kinetic, equilibrium and thermodynamic studies suggest that CLB biosorbs Cr ions from Cr(VI) aqueous solutions predominantly by a chemical sorption phenomenon. Low cost, availability, renewable nature, and effective total Cr biosorption make CLB a highly attractive and efficient method to remediate Cr(VI)-contaminated water and wastewater.

  11. Chromium Biosorption from Cr(VI) Aqueous Solutions by Cupressus lusitanica Bark: Kinetics, Equilibrium and Thermodynamic Studies

    Science.gov (United States)

    Netzahuatl-Muñoz, Alma Rosa; Cristiani-Urbina, María del Carmen; Cristiani-Urbina, Eliseo

    2015-01-01

    The present study investigated the kinetics, equilibrium and thermodynamics of chromium (Cr) ion biosorption from Cr(VI) aqueous solutions by Cupressus lusitanica bark (CLB). CLB total Cr biosorption capacity strongly depended on operating variables such as initial Cr(VI) concentration and contact time: as these variables rose, total Cr biosorption capacity increased significantly. Total Cr biosorption rate also increased with rising solution temperature. The pseudo-second-order model described the total Cr biosorption kinetic data best. Langmuir´s model fitted the experimental equilibrium biosorption data of total Cr best and predicted a maximum total Cr biosorption capacity of 305.4 mg g-1. Total Cr biosorption by CLB is an endothermic and non-spontaneous process as indicated by the thermodynamic parameters. Results from the present kinetic, equilibrium and thermodynamic studies suggest that CLB biosorbs Cr ions from Cr(VI) aqueous solutions predominantly by a chemical sorption phenomenon. Low cost, availability, renewable nature, and effective total Cr biosorption make CLB a highly attractive and efficient method to remediate Cr(VI)-contaminated water and wastewater. PMID:26352933

  12. Photoreduction of Cr(VI) in water using Bi{sub 2}O{sub 3}-ZrO{sub 2} nanocomposite under visible light irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Vignesh, Kumaravel [Post Graduate and Research Department of Chemistry, Thiagarajar College, Madurai 625009, Tamilnadu (India); Priyanka, Rajarajan [Department of Electrical and Electronics Engineering, Thiagarajar College of Engineering, Madurai 625015, Tamilnadu (India); Rajarajan, Muthuramalingam, E-mail: rajarajan_1962@yahoo.com [Department of Chemistry, Cardamom Planters' Association College, Bodinayakanur 626513, Tamilnadu (India); Suganthi, Ayyadurai, E-mail: suganthitcarts@gmail.com [Post Graduate and Research Department of Chemistry, Thiagarajar College, Madurai 625009, Tamilnadu (India)

    2013-02-01

    Highlights: Black-Right-Pointing-Pointer Bi{sub 2}O{sub 3}-ZrO{sub 2} nanocomposite was prepared by simple co-precipitation method. Black-Right-Pointing-Pointer PL measurements confirm the high suppression of electron-hole recombination. Black-Right-Pointing-Pointer The photocatalytic activity was measured by the reduction of Cr(VI). Black-Right-Pointing-Pointer The reaction conditions are optimized. Black-Right-Pointing-Pointer Bi{sub 2}O{sub 3}-ZrO{sub 2} was stable without loss of its activity up to 4 cyclic experiments. - Abstract: Chromium(VI) is a common heavy metal pollutant and extensively used in variety of industrial processes. In the present study, bismuth oxide-zirconium oxide nanocomposite (Bi{sub 2}O{sub 3}-ZrO{sub 2}) was synthesized to improve photoreduction of Cr(VI) under visible light irradiation. The synthesized photocatalyst was characterized by UV-visible-diffuse reflectance spectroscopy (UV-vis-DRS), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), Brunauer-Emmett-Teller (B.E.T) surface area analysis and photoluminescence spectroscopy (PL). Bi{sub 2}O{sub 3}-ZrO{sub 2} was found to be more photoactive than Bi{sub 2}O{sub 3}, ZrO{sub 2}, TiO{sub 2} and ZnO for the reduction of Cr (VI). The influences of various reaction parameters like the effect of catalyst concentration, initial Cr(VI) concentration and addition of inorganic salts on the photocatalytic activity have been investigated in detail. Meanwhile, the stability of Bi{sub 2}O{sub 3}-ZrO{sub 2} was investigated by repeatedly performing Cr(VI) photoreducing experiments.

  13. Improved Bi Film Wrapped Single Walled Carbon Nanotubes for Ultrasensitive Electrochemical Detection of Trace Cr(VI)

    Science.gov (United States)

    Zhou, Shilin; Xue, Zi-Ling; Xu, Lina; Gu, Yingying; Miao, Yuqing

    2014-01-01

    We report here the successful fabrication of an improved Bi film wrapped single walled carbon nanotubes modified glassy carbon electrode (Bi/SWNTs/GCE) as a highly sensitive platform for ultratrace Cr(VI) detection through catalytic adsorptive cathodic stripping voltammetry (AdCSV). The introduction of negatively charged SWNTs extraordinarily decreased the size of Bi particles to nanoscale due to electrostatic interaction which made Bi(III) cations easily attracted onto the surface of SWNTs in good order, leading to higher quality of Bi film deposition. The obtained Bi/SWNTs composite was well characterized with electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), the static water contact angle and the voltammetric measurements. The results demonstrates the improvements in the quality of Bi film deposited on the surface of SWNTs such as faster speed of electron transfer, more uniform and smoother morphology, better hydrophilicity and higher stripping signal. Using diethylene triaminepentaacetic acid (DTPA) as complexing ligand, the fabricated electrode displays a well-defined and highly sensitive peak for the reduction of Cr(III)-DTPA complex at −1.06 V (vs. Ag/AgCl) with a linear concentration range of 0–25 nM and a fairly low detection limit of 0.036 nM. No interference was found in the presence of coexisting ions, and good recoveries were achieved for the analysis of a river sample. In comparison to previous approaches using Bi film modified GCE, the newly designed electrode exhibits better reproducibility and repeatability towards aqueous detection of trace Cr(VI) and appears to be very promising as the basis of a highly sensitive and selective voltammetric procedure for Cr(VI) detection at trace level in real samples. PMID:24771881

  14. Over-expression of superoxide dismutase ameliorates Cr(VI induced adverse effects via modulating cellular immune system of Drosophila melanogaster.

    Directory of Open Access Journals (Sweden)

    Prakash Pragya

    Full Text Available The evolutionarily conserved innate immune system plays critical role for maintaining the health of an organism. However, a number of environmental chemicals including metals are known to exert adverse effects on immune system. The present study assessed the in vivo effect of a major environmental chemical, Cr(VI, on cellular immune response using Drosophila melanogaster and subsequently the protective role of superoxide dismutase (SOD based on the comparable performance of the tested anti-oxidant enzymes. The immuno-modulatory potential of Cr(VI was demonstrated by observing a significant reduction in the total hemocyte count along with impaired phagocytic activity in exposed organism. Concurrently, a significant increase in the percentage of Annexin V-FITC positive cells, activation of DEVDase activity, generation of free radical species along with inhibition of anti-oxidant enzyme activities was observed in the hemocytes of exposed organism. In addition, we have shown that ONOO(- is primarily responsible for Cr(VI induced adverse effects on Drosophila hemocytes along with O2(-. While generation of O2(-/ONOO(- in Cr(VI exposed Drosophila hemocytes was found to be responsible for the suppression of Drosophila cellular immune response, Cr(VI induced alteration was significantly reduced by the over-expression of sod in Drosophila hemocytes. Overall, our results suggest that manipulation of one of the anti-oxidant genes, sod, benefits the organism from Cr(VI induced alteration in cellular immunity. Further, this study demonstrates the applicability of D. melanogaster to examine the possible effects of environmental chemicals on innate immunity which can be extrapolated to higher organisms due to evolutionary conservation of innate immune system between Drosophila and mammals.

  15. Efficient removal of Cr(III)-organic complexes from water using UV/Fe(III) system: Negligible Cr(VI) accumulation and mechanism.

    Science.gov (United States)

    Ye, Yuxuan; Jiang, Zhao; Xu, Zhe; Zhang, Xiaolin; Wang, Dandan; Lv, Lu; Pan, Bingcai

    2017-12-01

    Most available processes are incapable of removing Cr(III)-organic complexes from water due to their high solubility, extremely slow decomplexation rate, and possible formation of more toxic Cr(VI) during oxidation. Herein, we proposed a new combined process, i.e., UV/Fe(III) followed by alkaline precipitation (namely UV/Fe(III)+OH), to achieve highly efficient and environmentally benign removal of Cr(III)-organic complexes from water. The combined process could remove Cr(III)-citrate from 10.4 mg Cr/L to 0.36 mg Cr/L and ∼60% total organic carbon as well. More attractively, negligible Cr(VI) (Fe(III) generates ·OH radicals to transform Cr(III) into Cr(VI) and simultaneously released the citrate ligand to form Fe(III)-citrate simultaneously. Then, the photolysis of Fe(III)-citrate under UV irradiation involved the citrate degradation and the production of massive Fe(II) species, which in turn transformed the formed Cr(VI) back to Cr(III). The free metal ions, including Cr(III), Fe(II) and Fe(III) were removed by the subsequent alkaline precipitation. Also, the combined process is applicable to other Cr(III) complexes with EDTA, tartrate, oxalate, acetate. The applicability of the combined process was further demonstrated by treating two real tanning effluents, resulting in the residual Cr(III) below 1.5 mg/L (the discharge standard of China) and negligible formation of Cr(VI) (<0.004 mg/L) as well. In general, the combined process has a great potential for efficient removal of Cr(III) complexes from contaminated waters. Copyright © 2017 Elsevier Ltd. All rights reserved.

  16. Chromium (VI) adsorption from wastewater using porous magnetite nanoparticles prepared from titanium residue by a novel solid-phase reduction method.

    Science.gov (United States)

    Ren, Genkuan; Wang, Xinlong; Huang, Penghui; Zhong, Benhe; Zhang, Zhiye; Yang, Lin; Yang, Xiushan

    2017-12-31

    Porous magnetite nanoparticles were successfully synthesized by reduction of titanium residue with pyrite under nitrogen protection, and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, energy dispersive X-ray spectroscopy, vibrating sample magnetometer, X-ray photoelectron spectroscope, zeta potential and Brunauer-Emmett-Teller method. The XRD analysis confirmed the formation of porous magnetite nanoparticles with single spinel structure. The SEM image demonstrated that porous magnetite nanoparticles displayed spherical shape with the average diameter of ~51nm. The surface area of porous magnetite nanoparticles with high magnetic moment (78emu·g(-1)) was 11.1m(2)g(-1). The experimental results revealed that equilibrium adsorption behavior of Cr(VI) was well described by Langmuir isotherm model with the maximum adsorption capacity of 14.49mgg(-1) at 298.15K, and kinetic data was found to fit well with pseudo-second-order model. The adsorption rate for Cr(VI) was controlled by both boundary layer diffusion and intraparticle diffusion. Thermodynamics analysis showed that the adsorption processes of Cr(VI) were endothermic and spontaneous. In addition, the adsorption of Cr(VI) on porous magnetite nanoparticles was classified as chemisorption adsorption, which depended on electrostatic attraction accompanied with reduction of Cr(VI) to Cr(III). Porous magnetite nanoparticles were readily regenerated and used repeatedly for Cr(VI) adsorption at least five cycles. Furthermore, the experimental results indicate that porous magnetite nanoparticles have a promising application for Cr(VI) adsorption from wastewater. Copyright © 2017 Elsevier B.V. All rights reserved.

  17. Estudio de materiales adsorbentes de bajo costo para remover Cr(VI de efluentes acuosos

    Directory of Open Access Journals (Sweden)

    Claudia Vargas-Niño

    2011-01-01

    Full Text Available El presente estudio muestra el enorme potencial de dos tipos de sólidos diferentes, una alúmina comercial y un material producto del compostaje, en la adsorción/eliminación de Cr(VI en medio acuoso, en concentraciones de metal equivalentes a las halladas en aguas residuales provenientes de industrias en Colombia. Ambos materiales mostraron propiedades importantes para la eliminación de Cr(VI, considerándose de mayor relevancia el compost por ser un material de bajo costo. Se establecieron las condiciones óptimas para la adsorción de cromo sobre alúmina y sobre compost. Para la alúmina: concentración inicial de Cr(VI = 10 mgL-1, volumen de solución por masa de adsorbente = 100 mL/g, pH = 2,0, tiempo de equilibrio = 1 hora, y agitación = 150 rpm. Para el compost: concentración inicial de Cr(VI = 3 mg L-1, volumen de solución por masa de adsorbente = 50 mL/g, pH = 2.5, tiempo de equilibrio = 3 horas, y agitación = 150 rpm. Además, los resultados mostraron que las propiedades de adsorción del compost se pueden mejorar mediante la adición de pequeñas cantidades de alúmina. El estudio permitió seleccionar al compost como un material promisorio para procedimientos de remediación de aguas residuales que contienen cromo (VI dentro de una política de manejo y uso de residuos sólidos con el objeto de minimizar el impacto ambiental de éstos.

  18. The applications of populus fiber in removal of Cr{sup (VI)} from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Li, Miaomiao; Gong, Yumei, E-mail: ymgong@dlpu.edu.cn; Lyu, Aichao; Liu, Yuanfa, E-mail: morning309@126.com; Zhang, Hong, E-mail: zhang_hong1234@sina.com

    2016-10-15

    Highlights: • A sorbent for heavy metal ions based on populus fibers is prepared by a green way. • The chromium adsorption on the sorbent accords with the pseudo-second-order kinetics. • The proposed adsorption involves static attraction and chelation by the sorbent on chromium. • The sorbent is expected to be applied in universal conditions. - Abstract: The surface modification of natural materials to be applied in removal of Cr{sup (VI)} from aqueous solutions has attracted much attention. A natural sorbent for Cr{sup (VI)} based on natural populus fibers (PF) is prepared by transforming the cyano groups (AN) in polyacrylonitriles (PAN) grafted from PF into amidoxime groups (AO), which has strong ability to attract and chelate heavy metal ions. The prepared sorbent is characterized by Fourier Transform Infrared Spectra (FT-IR), thermogravimetric analysis (TGA), solid-state nuclear magnetic resonance ({sup 13}C NMR) and scanning electron microscope (SEM). As potassium dichromate solution (K{sub 2}Cr{sub 2}O{sub 7}) is used as a target solution for detecting adsorption capacity of the sorbent, the adsorption kinetics of the sorbent for chromiun is consistent with the pseudo-second-order kinetic model by analyzing the adsorption amount as a function of the sorbent dispersed duration in solution at pH = 2. The expected adsorption mechanism is that the Cr{sup (VI)} in anionic ions Cr{sub 2}O{sub 7}{sup 2−} and HCrO{sub 4}{sup −} are adsorbed through electrostatic attraction but when Cr{sup (VI)} is reduced to Cr{sup (III)} by AO, the electronegative nitrogen and oxygen in AO chelate it through coordination bond. The as-prepared PF derivant with high adsorption efficiency of chromium 180.5 mg/g (3.47 mmol/g), low cost, reusability and greenly preparation process suggests that the development of natural PF as a sorbent in removal of Cr{sup (VI)} from aqueous solutions is a destined significant approach.

  19. BIOSORCIÓN OF Cr (VI) BY LEMON RIND, CITRUS LIMONIUM, TREATED

    OpenAIRE

    Armijo C., Javier; Departamento de Operaciones Unitarias, Facultad de Química e Ingeniería Química-Universidad Nacional Mayor de San Marcos. Lima-Perú; Rivera, Dolores; Departamento de Química Analítica, Facultad de Química e Ingeniería Química-Universidad Nacional Mayor de San Marcos. Lima-Perú; Mallma C., Gliseth; Tesista de lng. Química , Facultad de Química e Ingeniería Química-Universidad Nacional Mayor de San Marcos. Lima-Perú

    2014-01-01

    We tested biosorcion of chromium (VI) using lemon rind, citrus limonium, treated. The original lemon rind passes first through a stage of desmetoxilación with sodium hydroxide solution, 0.2M, pH 10, and in a second stage is subject to a process of crosslinking with solution diclorurm calcium, 0.2M, pH 2. The tests showed that chromium (VI) can be removed from its aqueous solutions, up to 75% of its initial concentration in twenty minutes. Se han realizado ensayos de biosorción de cr...

  20. The surface characteristics of hyperbranched polyamide modified corncob and its adsorption property for Cr(VI)

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Hai, E-mail: linhai@ces.ustb.edu.cn [School of Energy and Environmental Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Beijing Key Laboratory on Resource-oriented Treatment of Industrial Pollutants, Beijing 100083 (China); Han, Shaoke; Dong, Yingbo; He, Yinhai [School of Energy and Environmental Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Beijing Key Laboratory on Resource-oriented Treatment of Industrial Pollutants, Beijing 100083 (China)

    2017-08-01

    Highlights: • An anion adsorbent was synthesized by hyperbranched polyamide modified corncob (HPMC). • The surface characteristics of samples (RCC, HPMC, HPMC-Cr) were studied. • Langmuir isotherm provided more fit and maximum adsorption capacity was 131.6 mg/g. • The adsorption process was chemisorption, controlled by intra-particle diffusion and film diffusion. • Adsorption is fast, stable, spontaneous and endothermic. - Abstract: A low-cost anion adsorbent for Cr(VI) effectively removing was synthesized by hyperbranched polyamide modified corncob (HPMC). Samples were characterized by Brunauer–Emmett–Teller (BET) surface area analysis, field-emission scanning electron microscopy (FE-SEM) with energy-dispersive X-ray spectroscopy, Fourier transform infrared (FTIR) and zeta potential analysis. Kinetics, isotherms and thermodynamics studies of HPMC for Cr(VI) adsorption were investigated in batch static experiments, in the temperature range of 25–45 °C, pH = 2.0. Results showed that the adsorption was rapid and stable, with the uptake capacity higher than 80% after 30 min. Adsorption behavior and rate-controlling mechanisms were analyzed using three kinetic models (pseudo-first order, pseudo-second order, intra-particle kinetic model). Kinetic studies showed that the adsorption of HPMC to Cr(VI) relied the pseudo-second-order model, and controlled both by the intra-particle diffusion and film diffusion. Equilibrium data was tested by Langmuir and Freundlich adsorption isotherm models. Langmuir model was more suitable to indicate a homogeneous distribution of active sites on HPMC and monolayer adsorption. The maximum adsorption capacity from the Langmuir model, q{sub max}, was 131.6 mg/g at pH 2.0 and 45 °C for HPMC. Thermodynamic parameters revealed spontaneous and endothermic nature of the Cr(VI) adsorption onto HPMC.

  1. Melanin-embedded materials effectively remove hexavalent chromium (CrVI) from aqueous solution.

    Science.gov (United States)

    Cuong, An Manh; Le Na, Nguyen Thi; Thang, Pham Nhat; Diep, Trinh Ngoc; Thuy, Ly Bich; Thanh, Nguyen Lai; Thang, Nguyen Dinh

    2018-02-23

    Currently, it is recognized that water polluted with toxic heavy metal ions may cause serious effects on human health. Therefore, the development of new materials for effective removal of heavy metal ions from water is still a widely important area. Melanin is being considered as a potential material for removal of heavy metal from water. In this study, we synthesized two melanin-embedded beads from two different melanin powder sources and named IMB (Isolated Melanin Bead originated from squid ink sac) and CMB (Commercial Melanin Bead originated from sesame seeds). These beads were of globular shape and 2-3 mm in diameter. We investigated and compared the sorption abilities of these two bead materials toward hexavalent-chromium (Cr VI ) in water. The isotherm sorption curves were established using Langmuir and Freundlich models in the optimized conditions of pH, sorption time, solid/liquid ratio, and initial concentration of Cr VI . The FITR analysis was also carried out to show the differences in surface properties of these two beads. The optimized conditions for isotherm sorption of Cr VI on IMB/CMB were set at pH values of 2/2, sorption times of 90/300 min, and solid-liquid ratios of 10/20 mg/mL. The maximum sorption capacities calculated based on the Langmuir model were 19.60 and 6.24 for IMB and CMB, respectively. However, the adsorption kinetic of Cr VI on the beads fitted the Freundlich model with R 2 values of 0.992 for IMB and 0.989 for CMB. The deduced Freundlich constant, 1/n, in the range of 0.2-0.8 indicated that these beads are good adsorption materials. In addition, structure analysis data revealed great differences in physical and chemical properties between IMB and CMB. Interestingly, FTIR analysis results showed strong signals of -OH (3295.35 cm - 1 ) and -C=O (1608.63 cm - 1 ) groups harboring on the IMB but not CMB. Moreover, loading of Cr VI on the IMB caused a shift of broad peaks from 3295.35 cm - 1 and 1608.63 cm - 1 to 3354

  2. The application of tree bark as bio-indicator for the assessment of Cr(VI) in air pollution

    Energy Technology Data Exchange (ETDEWEB)

    Mandiwana, Khakhathi L. [Department of Chemistry, Tshwane University of Technology, Private Bag X31, Rosslyn 0200 (South Africa)]. E-mail: MandiwanaKL@tut.ac.za; Resane, Tabby [School of Geosciences, University of Witwatersrand, Johannesburg (South Africa); Panichev, Nikolay [Department of Chemistry, Tshwane University of Technology, Private Bag X31, Rosslyn 0200 (South Africa); Ngobeni, Prince [Department of Chemistry, Tshwane University of Technology, Private Bag X31, Rosslyn 0200 (South Africa)

    2006-09-21

    The impact of a chromium smelter on pollution was evaluated by determining Cr(VI) in topsoil, grass and tree bark by electhrothermal atomic absorption spectrometry (ETAAS). It was found that bark reflected the levels of air pollution better than soil and grass due to its high accumulative ability of Cr(VI). The tree bark was contaminated with Cr(VI) by a factor of 9 than in soil. It is therefore suggested that the bark be used as an indicator of air pollution for long-term exposure. The concentration of Cr(VI) in the bark was always a fraction of the total concentration of Cr and ranges between 1.6 and 3%. The method used in the preparation of samples was validated by the analysis of certified reference materials.

  3. The application of tree bark as bio-indicator for the assessment of Cr(VI) in air pollution.

    Science.gov (United States)

    Mandiwana, Khakhathi L; Resane, Tabby; Panichev, Nikolay; Ngobeni, Prince

    2006-09-21

    The impact of a chromium smelter on pollution was evaluated by determining Cr(VI) in topsoil, grass and tree bark by electrothermal atomic absorption spectrometry (ETAAS). It was found that bark reflected the levels of air pollution better than soil and grass due to its high accumulative ability of Cr(VI). The tree bark was contaminated with Cr(VI) by a factor of 9 than in soil. It is therefore suggested that the bark be used as an indicator of air pollution for long-term exposure. The concentration of Cr(VI) in the bark was always a fraction of the total concentration of Cr and ranges between 1.6 and 3%. The method used in the preparation of samples was validated by the analysis of certified reference materials.

  4. Quercetin inhibits Cr(VI)-induced malignant cell transformation by targeting miR-21-PDCD4 signaling pathway.

    Science.gov (United States)

    Pratheeshkumar, Poyil; Son, Young-Ok; Divya, Sasidharan Padmaja; Wang, Lei; Turcios, Lilia; Roy, Ram Vinod; Hitron, John Andrew; Kim, Donghern; Dai, Jin; Asha, Padmaja; Zhang, Zhuo; Shi, Xianglin

    2017-08-08

    Hexavalent chromium [Cr(VI)] is an important human carcinogen associated with pulmonary diseases and lung cancer. Inhibition of Cr(VI)-induced carcinogenesis by a dietary antioxidant is a novel approach. Quercetin is one of the most abundant dietary flavonoids widely present in many fruits and vegetables, possesses potent antioxidant and anticancer properties. MicroRNA-21 (miR-21) is a key oncomiR significantly elevated in the majority of human cancers that exerts its oncogenic activity by targeting the tumor suppressor gene programmed cell death 4 (PDCD4). The present study examined the effect of quercetin on the inhibition of Cr(VI)-induced malignant cell transformation and the role of miR-21-PDCD4 signaling involved. Our results showed that quercetin decreased ROS generation induced by Cr(VI) exposure in BEAS-2B cells. Chronic Cr(VI) exposure induced malignant cell transformation, increased miR-21 expression and caused inhibition of PDCD4, which were significantly inhibited by the treatment of quercetin in a dose dependent manner. Nude mice injected with BEAS-2B cells chronically exposed to Cr(VI) in the presence of quercetin showed reduced tumor incidence compared to Cr(VI) alone treated group. Stable knockdown of miR-21 and overexpression of PDCD4 or catalase in BEAS-2B cells suppressed Cr(VI)-induced malignant transformation and tumorigenesis. Taken together, these results demonstrate that quercetin is able to protect BEAS-2B cells from Cr(VI)-induced carcinogenesis by targeting miR-21-PDCD4 signaling.

  5. As(V)/Cr(VI) retention on un-amended and waste-amended soil samples: competitive experiments.

    Science.gov (United States)

    Rivas-Pérez, Ivana M; Conde-Cid, Manuel; Nóvoa-Muñoz, Juan Carlos; Arias-Estévez, Manuel; Fernández-Sanjurjo, María J; Álvarez-Rodríguez, Esperanza; Núñez-Delgado, Avelino

    2017-01-01

    Focusing on simultaneous arsenic and chromium pollution, we used batch-type experiments to study As(V)/Cr (VI) competitive sorption on soil samples, pyritic material, mussel shell, oak ash, pine bark and hemp waste, as well as on binary mixtures (50 % mussel shell and 50 % another material-oak ash, pine bark, or hemp waste), and on forest and vineyard soil samples and pyritic material amended with 48 t ha(-1) of mussel shell, oak ash, pine bark, or hemp waste. Equal As(V) and Cr(VI) concentrations (0 to 6 mmol L(-1)) were added to the individual materials, binary mixtures, and 48 t ha(-1) amended materials. The individual forest soil sample, pyritic material, and oak ash showed clearly higher As(V) sorption, whereas Cr(VI) sorption was higher on pine bark. Sorption was up to 50 % higher for As(V) than for Cr(VI) on the forest soil sample, oak ash, and pyritic material, while pine bark sorbed 95 % more Cr(VI). Regarding binary mixtures, the presence of mussel shell increased As(V) sorption on pine bark and Cr(VI) sorption on hemp waste. As regards the amendments, in the case of the forest soil sample, the amendments with oak ash and mussel shell increased As(V) sorption, while pine bark amendment increased Cr(VI) sorption; in the vineyard soil sample, the mussel shell amendment increased As(V) sorption; in the pyritic material, pine bark amendment increased Cr(VI) sorption. These results could be useful to appropriately manage the soils and individual or mixed by-products assayed when As(V) and Cr(VI) pollution occurs.

  6. The Protective Role of Hyaluronic Acid in Cr(VI-Induced Oxidative Damage in Corneal Epithelial Cells

    Directory of Open Access Journals (Sweden)

    Wei Wu

    2017-01-01

    Full Text Available Cr(VI exposure could produce kinds of intermediates and reactive oxygen species, both of which were related to DNA damage. Hyaluronan (HA has impressive biological functions and was reported to protect corneal epithelial cells against oxidative damage induced by ultraviolet B, benzalkonium chloride, and sodium lauryl sulfate. So the aim of our study was to investigate HA protection on human corneal epithelial (HCE cells against Cr(VI-induced toxic effects. The HCE cell lines were exposed to different concentrations of K2Cr2O7 (1.875, 3.75, 7.5, 15.0, and 30 μM or a combination of K2Cr2O7 and 0.2% HA and incubated with different times (15 min, 30 min, and 60 min. Our data showed that Cr(VI exposure could cause decreased cell viability, increased DNA damage, and ROS generation to the HCE cell lines. But incubation of HA increased HCE cell survival rates and decreased DNA damage and ROS generation induced by Cr(VI in a dose- and time-dependent manner. We report for the first time that HA can protect HCE cells against the toxicity of Cr(VI, indicating that it will be a promising therapeutic agent to corneal injuries caused by Cr(VI.

  7. Adsorption Properties of Bentonite with In Situ Immobilized Polyaniline Towards Anionic Forms of Cr(VI, Mo(VI, W(VI, V(V

    Directory of Open Access Journals (Sweden)

    Kateryna RYABCHENKO

    2016-05-01

    Full Text Available A new composite material bentonite-PANI was synthesized by in situ immobilization of polyaniline (PANI on the surface of natural mineral bentonite. It was established as a result of the modification of bentonite a surface area and an interlayer distance of mineral decrease and particles of bentonite transformed of irregular shape with different porosity on irregularly shaped particles of smaller size. It has been found that the total Cr(VI ions extraction took place under the acid conditions (pH=1 – 2 and W(VI ions have been well adsorbed in the pH range from 1 to 8 by the composite bentonite-PANI unlike the initial mineral. Whereas adsorption of oxo anions of V(V and Mo(VI made up some 50%. It is proved that the in situ immobilization of bentonite by polyaniline leads to increasing the value of adsorption capacity towards the investigated ions compared with the initial mineral. It was established that the adsorption properties of the synthesized composite with respect to the studied oxo ions were worse than the adsorption properties of composite vermiculite-PANI, similar to the composite Sokyryntsyy clinoptilolite-PANI and better than composites of polyaniline with Podilskyy saponite and Karelian shungite.DOI: http://dx.doi.org/10.5755/j01.ms.22.2.6976

  8. Importance of c-Type cytochromes for U(VI reduction by Geobacter sulfurreducens

    Directory of Open Access Journals (Sweden)

    Leang Ching

    2007-03-01

    Full Text Available Abstract Background In order to study the mechanism of U(VI reduction, the effect of deleting c-type cytochrome genes on the capacity of Geobacter sulfurreducens to reduce U(VI with acetate serving as the electron donor was investigated. Results The ability of several c-type cytochrome deficient mutants to reduce U(VI was lower than that of the wild type strain. Elimination of two confirmed outer membrane cytochromes and two putative outer membrane cytochromes significantly decreased (ca. 50–60% the ability of G. sulfurreducens to reduce U(VI. Involvement in U(VI reduction did not appear to be a general property of outer membrane cytochromes, as elimination of two other confirmed outer membrane cytochromes, OmcB and OmcC, had very little impact on U(VI reduction. Among the periplasmic cytochromes, only MacA, proposed to transfer electrons from the inner membrane to the periplasm, appeared to play a significant role in U(VI reduction. A subpopulation of both wild type and U(VI reduction-impaired cells, 24–30%, accumulated amorphous uranium in the periplasm. Comparison of uranium-accumulating cells demonstrated a similar amount of periplasmic uranium accumulation in U(VI reduction-impaired and wild type G. sulfurreducens. Assessment of the ability of the various suspensions to reduce Fe(III revealed no correlation between the impact of cytochrome deletion on U(VI reduction and reduction of Fe(III hydroxide and chelated Fe(III. Conclusion This study indicates that c-type cytochromes are involved in U(VI reduction by Geobacter sulfurreducens. The data provide new evidence for extracellular uranium reduction by G. sulfurreducens but do not rule out the possibility of periplasmic uranium reduction. Occurrence of U(VI reduction at the cell surface is supported by the significant impact of elimination of outer membrane cytochromes on U(VI reduction and the lack of correlation between periplasmic uranium accumulation and the capacity for uranium

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

    DEFF Research Database (Denmark)

    Diacu, Elena; Andersen, Jens Enevold Thaulov

    2003-01-01

    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 showed...... that it was possible to obtain reliable predictions of Cr(III) and Cr(VI) species. The method was validated on samples of stainless steel. In order to facilitate analysis of stainless-steel samples it was essential to perform a step of evaporation to dryness followed by re-dissolution. The analysis showed that species...

  10. Speciation of Cr(III) and Cr(VI) in geological and water samples by ytterbium(III) hydroxide coprecipitation system and atomic absorption spectrometry.

    Science.gov (United States)

    Duran, Ali; Tuzen, Mustafa; Soylak, Mustafa

    2011-07-01

    A novel coprecipitation method with ytterbium(III) hydroxide has been established for speciation of Cr(III) and Cr(VI) in geological and water samples. At pH 10, while Cr(III) was quantitatively recovered, Cr(VI) was recovered under 10% levels. Total chromium was determined reducing of Cr(VI) to Cr(III) in acidic media with KI reagent. The concentration of Cr(VI) was calculated by the concentration difference between the total chromium and Cr(III). For the quantitative recovery of Cr(III), parameters such as pH, amount of ytterbium, centrifugation time and speed, matrix effect, KI amount, and sample volume were investigated. The preconcentration factor was 30. The limit of detection was obtained as 1.1 μg/L for Cr(III). The accuracy was checked by analyte addition and analyses of standard reference materials (TMDA-54.4 Certified Reference Water, NIST 2710 Montana Soil). Method has been successfully applied to the chromium speciation for industrial waste water of leather factories located in Bor-Nigde, and also for mine and soil samples. Copyright © 2011 Elsevier Ltd. All rights reserved.

  11. THE INFLUENCE OF POTASSIUM DICHROMATE Cr (VI ADMINISTRATION DURATION ON GLOBULAR RESISTANCE IN FEMALE RATS

    Directory of Open Access Journals (Sweden)

    LETIŢIA STANA

    2009-05-01

    Full Text Available The „in vivo” experiment has had as aim the study of different Cr(VI doses administration on globular resistance in female rats related to administration duration. Study was carried out on 56 female rats divided in 8 groups, 6 experimental and 2 control that received potassium dichromate in drinking water in doses of 25 ppm, 50 ppm and 75ppm Cr(VI, for 3 months, respectively, 6 months. Decrease of globular resistance (in terms of haemolysis degree in hypotonic solutions at increasing dose (up to 0.8% NaCl at 75 ppm dose in all experimental groups, in direct relation with the duration of administration was registered. Control groups were in physiological limits. The results of the present study revealed the affecting of erythrocyte membrane in function of administration duration and chromium intake level, because of oxidative lesions produced by it.

  12. Studies on enhancement of Cr(VI) biosorption by chemically modified biomass of Rhizopus nigricans.

    Science.gov (United States)

    Bai, R Sudha; Abraham, T Emilia

    2002-03-01

    This study reports the biosorption of Cr(VI) by chemically modified biomass of Rhizopus nigricans and the possible mechanism of Cr complexation to the adsorbent. The cell wall of this fungus possesses strong complexing property to effectively remove Cr(VI) anions from solution and wastewater. The mechanism of Cr adsorption by R. nigricans was ascertained by chemical modifications of the dead biomass followed by FTIR spectroscopic analysis of the cell wall constituents. Treatment of the biosorbent with mild alkalies (0.01 N NaOH and ammonia solution) and formaldehyde (10%, w/v) deteriorated the biosorption efficiency. However, extraction of the biomass powder in acids (0.1 N HCl and H2SO4), alcohols (50% v/v, CH3OH and C2H5OH) and acetone (50%, v/v) improved the Cr uptake capacity. Reaction of the cell wall amino groups with acetic anhydride reduced the biosorption potential drastically. Blocking of the-COOH groups by treatment with water soluble carbodiimide also resulted in initial lag in Cr binding. Biomass modification experiments conducted using Cetyl Trimethyl Ammonium Bromide (CTAB), Polyethylenimine (PEI), and Amino Propyl Trimethoxy Silane (APTS) improved the biosorption efficiency to exceptionally high levels. The FTIR spectroscopic analysis of the native, Cr bound and the other types of chemically modified biomass indicated the involvement of amino groups of Rhizopus cell wall in Cr binding. The adsorption data of the native and the most effectively modified biomass were evaluated by the Freundlich and the Langmuir adsorption isotherms and the possible adsorption phenomena are also discussed.

  13. Synchrotron Spectroscopic Studies of the Reaction of Cleaved Pyrite ( {FeS2}) Surfaces with Cr(VI) Solutions

    Science.gov (United States)

    Doyle, C. S.; Kendelewicz, T.; Bostick, B. C.; Brown, G. E.

    2002-12-01

    pHs of 2, 4, and 7. Additional studies were performed at pH 7 with 50 μM Cr(VI) for durations of 1 minute to 38 hours, and with 5 mM Cr(VI) for 30 seconds. Photoemission and X-ray Absorption Near Edge Structure (XANES) spectroscopies were performed under UHV conditions at beamline 10-1 at the Stanford Synchrotron Radiation Laboratory (SSRL). These studies show that chromate is an effective oxidizing agent for the pyrite surface and that oxidation products can be trapped on the pyrite surface under a reduced chromium layer. Sulfur 2p photoemission identified sulfate, sulfite and zero-valent sulfur species on the pyrite surface. The features due to sulfate and sulfite are broad and were fitted using a single broad envelope which may include contributions from disorder and varying degrees of hydration. Iron 2p photoemission and L-edge XANES showed that very minor amounts of iron (III) remain on the surface indicating that this species is rapidly lost into solution. The chromate was reductively sorbed onto the pyrite surface forming a (oxy)hydroxide layer which ultimately passivates the surface towards further chromium reduction or pyrite oxidation. We utilized synchrotron based PES and XAS to show that chromate is reductively sorbed at the pyrite surface, and that the pyrite oxidation products can be observed under a chromium (III) containing layer. These preliminary results indicate that reacting pyrite with Cr(VI) may play the dual role of reducing chromate and passivating pyrite surfaces towards oxidation.

  14. Electron transfer reaction of butane -1,3-diol and cr(vi) in aqueous ...

    African Journals Online (AJOL)

    Kinetic and mechanistic studies of electron transfer reaction of butane-1,3-diol and Cr(VI) ion in aqueous acidic medium have been carried out in aqueous medium at 271°C, I = 1.0 mol dm-3 (NaCl), [H +] = 0.5mol dm-3 (HCl). The reaction was inhibited by added anions and showed negative salt effect. Spectroscopic ...

  15. Speciation and separation of Cr(VI) and Cr(III) using coprecipitation with Ni2+/2-Nitroso-1-naphthol-4-sulfonic acid and determination by FAAS in water and food samples.

    Science.gov (United States)

    Uluozlu, Ozgur Dogan; Tuzen, Mustafa; Soylak, Mustafa

    2009-10-01

    A speciation procedure for chromium(III) and chromium(VI) in the water and food samples has been established in the presented work. The procedure presented based on quantitative recoveries of Cr(III)>95% using coprecipitation of Ni(2+)/2-Nitroso-1-naphthol-4-sulfonic acid. The total chromium was measured after reduction of Cr(VI) by concentrated H(2)SO(4) and ethanol. The Cr(VI) was calculated as the difference between the total Cr content and the Cr(III) contents. The analytical variables, pH, amounts of precipitate, sample volume for optimum recoveries of Cr(III) were investigated. The influences of the some alkaline and earth alkaline ions and some transition metals on the recoveries of analyte ions were also investigated. The preconcentration factor was 50. The detection limit (3 sigma) of the reagent blank for chromium(III) was 1.33 microg L(-1). The relative standard deviations for determinations were found to be bush branches and leaves (GBW 0703). The procedure was successfully applied to the speciation of chromium in natural water and food samples (fish, white cheese, cow's meat, black tea, boiled wheat).

  16. Adsorption and coadsorption mechanisms of Cr(VI) and organic contaminants on H3PO4 treated biochar.

    Science.gov (United States)

    Zhao, Nan; Zhao, Chuanfang; Lv, Yizhong; Zhang, Weifang; Du, Yuguo; Hao, Zhengping; Zhang, Jing

    2017-11-01

    The study of simultaneous removal of heavy metals and organic contaminants has practical applications due to the coexistence of complex pollutants in the wastewater or soil. In this work, biochar was prepared to study the removal efficiencies of Cr(VI), naphthalene (NAP) and bisphenol A (BPA) in the single or mixed systems. H3PO4-treated biochar presented a much higher adsorption capacity of the pollutants than the untreated biochar and also showed a high resistance to coexisting salts. The maximum adsorption capacities for Cr(VI) and BPA were 116.28 mg g(-1) and 476.19 mg g(-1), respectively. Coadsorption experiments revealed that the presence of organic pollutants caused a limited decrease (∼10%) of removal efficiency of Cr(VI) and no further decrease was observed with higher concentrations of organic pollutants, while the presence of Cr(VI) had little impact on the removal of NAP. Infrared spectra and molecular simulation demonstrated that Cr(VI) was mainly adsorbed on the biochar via chemical complexation, while the organic pollutants through π-π interaction. Unexpectedly, the addition of Cr(VI) increased the removal efficiency of BPA, probably due to the increased H-bond interactions between BPA and the biochar through bridge bonds of oxygenic groups from CrO4(2-). Copyright © 2017 Elsevier Ltd. All rights reserved.

  17. Tea waste biomass activated carbon electrode for simultaneous removal of Cr(VI) and fluoride by capacitive deionization.

    Science.gov (United States)

    Gaikwad, Mahendra S; Balomajumder, Chandrajit

    2017-10-01

    Capacitive deionization is promising less energy based desalination technique to achieve pure water. In the present study microporous activated carbon was prepared from tea waste biomass by chemical and thermal modification. Further TWBAC was used for preparation of the electrode. The TWBAC electrode was applied in the self-made CDI set up for simultaneous removal of hexavalent chromium [Cr(VI)] and fluoride (F) form mixed feed solution of Cr(VI) and F. The performance of TWBAC electrode was found effective for simultaneous removal of Cr(VI) and F from mixed feed solution. The maximum electrosorption capacity of Cr(VI) and F were found 0.77 and 0.74 mg g-1 for 10 mg L-1 and 2.83 and 2.49 mg g-1 for 100 mg L-1 mixed feed solution respectively. The higher removal of Cr(VI) was found due to the electrosorption selectivity of the divalent CrO42- is higher than that of the monovalent F-. Multicomponent isotherm modeling and kinetic study were carried out in this study. TWBAC CDI electrode could be useful for treatment of a low concentrated Cr(VI) and F containing wastewater. Copyright © 2017 Elsevier Ltd. All rights reserved.

  18. Determination of hexavalent chromium reduction using Cr stable isotopes: isotopic fractionation factors for permeable reactive barrier materials.

    Science.gov (United States)

    Basu, Anirban; Johnson, Thomas M

    2012-05-15

    Cr stable isotope measurements can provide improved estimates of the extent of Cr(VI) reduction to less toxic Cr(III). The relationship between observed (53)Cr/(52)Cr ratio shifts and the extent of reduction can be calibrated by determining the isotopic fractionation factor for relevant reactions. Permeable reactive barriers (PRB) made of Fe(0) and in situ redox manipulation (ISRM) zones effectively remediate Cr-contaminated aquifers. Here, we determine the isotopic fractionations for dominant reductants in reactive barriers and reduced sediments obtained from an ISRM zone at the US DOE's Hanford site. In all cases, significant isotopic fractionation was observed; fractionation (expressed as ε) was -3.91‰ for Fe(II)-doped goethite, -2.11‰ for FeS, -2.65‰ for green rust, -2.67‰ for FeCO(3), and -3.18‰ for ISRM zone sediments. These results provide a better calibration of the relationship between Cr isotope ratios and the extent of Cr(VI) reduction and aid in interpretation of Cr isotope data from systems with reactive barriers.

  19. Biosorption of Cr(VI from AqueousSolution Using New Adsorbent: Equilibrium and Thermodynamic Study

    Directory of Open Access Journals (Sweden)

    Israa G. Zainal

    2010-01-01

    Full Text Available Biosorption is one such emerging technology which utilized naturally occurring waste materials to sequester heavy metals from polluted water. In the present study cinnamon was utilized for Cr(VI removal from aqueous solutions.It was found that a time of two hours was sufficient for sorption to attain equilibrium. The optimum pH was 2 for Cr(VI removal. Temprature has little influence on the biosorption process. The Cr(VI removal decreased with increase in temperature. The biosorption data was well fitted to Dubinin - Radushkevich (D-R, Freundlich and Tempkin adsorption isotherm models, although the correlation coefficient of Langmuir model was high but the calculated adsorption capacity did not agree with the experimental. The thermodynamic study reveals that the biosorption process is spontaneous and the spontaneity decreased with temperature increase and the process is exothermic accompanied by highly ordered adsorbate at the solid liquid interface. ΔH° values were negative and lie in the range of physical adsorption.

  20. The bark of holm oak (Quercus ilex, L.) for airborne Cr(VI) monitoring.

    Science.gov (United States)

    Minganti, Vincenzo; Drava, Giuliana; De Pellegrini, Rodolfo; Anselmo, Marco; Modenesi, Paolo; Malaspina, Paola; Giordani, Paolo

    2015-01-01

    In this work, the bark of holm oak was used as a bioindicator to study the atmospheric distribution of Cr(VI). The chosen method (alkaline extraction and atomic absorption determination) was found in the literature, adapted for use with the matrix involved, and validated. The method had some limits, but provided an excellent estimation of Cr(VI) concentrations with good sensitivity and a reasonable time of analysis and cost. Thirty-four samples of holm oak collected in three areas characterised by different possible sources of pollution (the area near a former chromate production plant, an urban area, and a rural "reference" area) were analysed, obtaining concentrations ranging from 1.54 to 502 μg g(-1) near the industrial plant, ranging from 0.22 to 1.35 μg g(-1) in the urban area, and mostly below the detection limit (0.04 μg g(-1)) in the rural area. The bark of holm oak proved to be a good bioindicator to detect Cr(VI) in the environment. The extraction procedure followed by atomic absorption analysis is simple, provides good sensitivity, and it is suitable for environmental studies. Copyright © 2014 Elsevier Ltd. All rights reserved.

  1. Adsorption of Cr(VI) from aqueous solution by hydrous zirconium oxide.

    Science.gov (United States)

    Rodrigues, Liana Alvares; Maschio, Leandro José; da Silva, Rafael Evangelista; da Silva, Maria Lúcia Caetano Pinto

    2010-01-15

    A type of ZrO(2).nH(2)O was synthesized and its Cr(VI) removal potential was investigated in this study. The kinetic study, adsorption isotherm, pH effect, thermodynamic study and desorption were examined in batch experiments. The kinetic process was described by a pseudo-second-order rate model very well. The Cr(VI) adsorption tended to increase with a decrease of pH. The adsorption data fitted well to the Langmuir model. The adsorption capacity increased from 61 to 66 mg g(-1) when the temperature was increased from 298 to 338 K. The positive values of both Delta H degrees and DeltaS degrees suggest an endothermic reaction and increase in randomness at the solid-liquid interface during the adsorption. Delta G degrees values obtained were negative indicating a spontaneous adsorption process. The effective desorption of Cr(VI) on ZrO(2).nH(2)O could be achieved using distilled water at pH 12.

  2. Optimized Synthesis of FeS Nanoparticles with a High Cr(VI Removal Capability

    Directory of Open Access Journals (Sweden)

    Yuanyuan Liu

    2016-01-01

    Full Text Available FeS nanoparticles were synthesized using chemical precipitation method involving sulfide and ferrous solutions. Effects of important synthesis parameters including stabilizer, time taken for titration, horizontal oscillation speed, and initial salt concentration on the size of synthesized FeS nanoparticles were investigated by Orthogonal Array design. Increasing the CMC dosage significantly made the hydrodynamic diameter decrease between 0.05 wt.% and 0.15 wt.% while Na2S titration, oscillation rate, and Na2S concentration did not show significant influence on the hydrodynamic diameter of FeS nanoparticles. The synthesized FeS nanoparticles were characterized by using XRD (X-ray diffraction, TEM (transmission electron microscopy, and XPS (X-ray photoelectron spectroscopy. The as-synthesized FeS nanoparticles had an average size of 25 ± 10 nm and had a better long-term stability after storage for 150 days compared to bare FeS particles. Because of the optimized process parameters, the synthesized FeS nanoparticles had a higher Cr(VI removal capacity of 683 mg per gram of FeS in comparison to the previously reported cases, and up to 92.48% Cr(VI was removed from aqueous solutions. The small size, special surface property, and high reactivity make the synthesized FeS nanoparticles a promising tool for the remediation of Cr(VI contaminated soil and groundwater.

  3. Hybrid materials: Magnetite-Polyethylenimine-Montmorillonite, as magnetic adsorbents for Cr(VI) water treatment.

    Science.gov (United States)

    Larraza, Iñigo; López-Gónzalez, Mar; Corrales, Teresa; Marcelo, Gema

    2012-11-01

    Hybrid materials formed by the combination of a sodium rich Montmorillonite (MMT), with magnetite nanoparticles (40 nm, Fe(3)O(4) NPs) coated with Polyethylenimine polymer (PEI 800 g/mol or PEI 25000 g/mol) were prepared. The intercalation of the magnetite nanoparticles coated with PEI among MMT platelets was achieved by cationic exchange. The resulting materials presented a high degree of exfoliation of the MMT sheets and a good dispersion of Fe(3)O(4) NPs on both the surface and among the layers of MMT. The presence of amine groups in the PEI structure not only aids the exfoliation of the MMT layers, but also gives to the hybrid material the necessary functionality to interact with heavy metals. These hybrid materials were used as magnetic sorbent for the removal of hexavalent chromium from water. The effect that pH, Cr(VI) concentration, and adsorbent material composition have on the Cr(VI) removal efficiency was studied. A complete characterization of the materials was performed. The hybrid materials showed a slight dependence of the removal efficiency with the pH in a wide range (1-9). A maximum amount of adsorption capacity of 8.8 mg/g was determined by the Langmuir isotherm. Results show that these hybrid materials can be considered as potential magnetic adsorbent for the Cr(VI) removal from water in a wide range of pH. Copyright © 2012 Elsevier Inc. All rights reserved.

  4. Sorption studies on Cr (VI) removal from aqueous solution using cellulose grafted with acrylonitrile monomer.

    Science.gov (United States)

    Hajeeth, T; Sudha, P N; Vijayalakshmi, K; Gomathi, T

    2014-05-01

    Graft copolymerization of acrylonitrile on to cellulosic material derived from sisal fiber can be initiated effectively with ceric ammonium nitrate. The grafting conditions were optimized by changing the concentration of initiator and monomer. The change in crystallinity of the grafted polymeric samples was concluded from the XRD patterns. The prepared cellulose grafted acrylonitrile copolymer was used as an adsorbent to remove Cr (VI) ions from aqueous solutions. The efficiency of the adsorbent was identified from the variation in the percentage of adsorption with contact time, adsorbent dose and pH. From the observed results it was evident that the adsorption of metal ions increases with the increase in contact time and metal ion concentration. An optimum pH was found to be 5.0 for the removal of Cr (VI) from the aqueous solution. The results of the Langmuir, Freundlich, and pseudo first- and second-order studies revealed that the adsorption was found to fit well with Freundlich isotherm and follows pseudo second-order kinetics. From the above results, it was concluded that the cellulose-g-acrylonitrile copolymer was found to be an efficient adsorbent for the removal of Cr (VI) from aqueous waste generated from industries. Copyright © 2014 Elsevier B.V. All rights reserved.

  5. Magnetic solid-phase extraction combined with graphite furnace atomic absorption spectrometry for speciation of Cr(III) and Cr(VI) in environmental waters.

    Science.gov (United States)

    Jiang, Hong-mei; Yang, Ting; Wang, Yan-hong; Lian, Hong-zhen; Hu, Xin

    2013-11-15

    A new approach of magnetic solid phase extraction (MSPE) coupled with graphite furnace atomic absorption spectrometry (GFAAS) has been developed for the speciation of Cr(III) and Cr(VI) using zincon-immobilized silica-coated magnetic Fe3O4 nanoparticles (Zincon-Si-MNPs) as the MSPE absorbent. Cr(III) was quantitatively reserved on the absorbent at pH 9.1 while total Cr was reserved at pH 6.5. The absorbed Cr species were eluted by using 2 mol/L HCl and detected by GFAAS. The concentration of Cr(VI) could be calculated by subtracting Cr(III) from total Cr. All the parameters affecting the separation and extraction efficiency of Cr species such as pH, extraction time, concentration and volume of eluent, sample volume and influence of co-existing ions were systematically examined and the optimized conditions were established accordingly. The detection limit (LOD) of the method was 0.016 and 0.011 ng mL(-1) for Cr(III) and Cr(VI), respectively, with the enrichment factor of 100 and 150. The precisions of this method (Relative standard deviation, RSD, n=7) for Cr(III) and Cr(VI) at 0.1 ng mL(-1) were 6.0% and 6.2%, respectively. In order to validate the proposed method, a certified reference material of environmental water was analyzed, and the result of Cr speciation was in good agreement with the certified value. This MSPE-GFAAS method has been successfully applied for the speciation of Cr(III) and Cr(VI) in lake and tap waters with the recoveries of 88-109% for the spiked samples. Moreover, the MSPE separation mechanism of Cr(III) and Cr(VI) based on their adsorption-desorption on Zincon-Si-MNPs has been explained through various spectroscopic characterization. © 2013 Elsevier B.V. All rights reserved.

  6. Nitrification inhibition by hexavalent chromium Cr(VI)--Microbial ecology, gene expression and off-gas emissions.

    Science.gov (United States)

    Kim, Young Mo; Park, Hongkeun; Chandran, Kartik

    2016-04-01

    The goal of this study was to investigate the responses in the physiology, microbial ecology and gene expression of nitrifying bacteria to imposition of and recovery from Cr(VI) loading in a lab-scale nitrification bioreactor. Exposure to Cr(VI) in the reactor strongly inhibited nitrification performance resulting in a parallel decrease in nitrate production and ammonia consumption. Cr(VI) exposure also led to an overall decrease in total bacterial concentrations in the reactor. However, the fraction of ammonia oxidizing bacteria (AOB) decreased to a greater extent than the fraction of nitrite oxidizing bacteria (NOB). In terms of functional gene expression, a rapid decrease in the transcript concentrations of amoA gene coding for ammonia oxidation in AOB was observed in response to the Cr(VI) shock. In contrast, transcript concentrations of the nxrA gene coding for nitrite oxidation in NOB were relatively unchanged compared to Cr(VI) pre-exposure levels. Therefore, Cr(VI) exposure selectively and directly inhibited activity of AOB, which indirectly resulted in substrate (nitrite) limitation to NOB. Significantly, trends in amoA expression preceded performance trends both during imposition of and recovery from inhibition. During recovery from the Cr(VI) shock, the high ammonia concentrations in the bioreactor resulted in an irreversible shift towards AOB populations, which are expected to be more competitive in high ammonia environments. An inadvertent impact during recovery was increased emission of nitrous oxide (N2O) and nitric oxide (NO), consistent with recent findings linking AOB activity and the production of these gases. Therefore, Cr(VI) exposure elicited multiple responses on the microbial ecology, gene expression and both aqueous and gaseous nitrogenous conversion in a nitrification process. A complementary interrogation of these multiple responses facilitated an understanding of both direct and indirect inhibitory impacts on nitrification. Copyright

  7. Synthesis, characterization and application of Lagerstroemia speciosa embedded magnetic nanoparticle for Cr(VI) adsorption from aqueous solution.

    Science.gov (United States)

    Srivastava, Shalini; Agrawal, Shashi Bhushan; Mondal, Monoj Kumar

    2017-05-01

    Lagerstroemia speciosa bark (LB) embedded magnetic nanoparticles were prepared by co-precipitation of Fe 2+ and Fe 3+ salt solution with ammonia and LB for Cr(VI) removal from aqueous solution. The native LB, magnetic nanoparticle (MNP), L. speciosa embedded magnetic nanoparticle (MNPLB) and Cr(VI) adsorbed MNPLB particles were characterized by SEM-EDX, TEM, BET-surface area, FT-IR, XRD and TGA methods. TEM analysis confirmed nearly spherical shape of MNP with an average diameter of 8.76nm and the surface modification did not result in the phase change of MNP as established by XRD analysis, while led to the formation of secondary particles of MNPLB with diameter of 18.54nm. Characterization results revealed covalent binding between the hydroxyl group of MNP and carboxyl group of LB particles and further confirmed its physico-chemical nature favorable for Cr(VI) adsorption. The Cr(VI) adsorption on to MNPLB particle as an adsorbent was tested under different contact time, initial Cr(VI) concentration, adsorbent dose, initial pH, temperature and agitation speed. The results of the equilibrium and kinetics of adsorption were well described by Langmuir isotherm and pseudo-second-order model, respectively. The thermodynamic parameters suggest spontaneous and endothermic nature of Cr(VI) adsorption onto MNPLB. The maximum adsorption capacity for MNPLB was calculated to be 434.78mg/g and these particles even after Cr(VI) adsorption were collected effortlessly from the aqueous solution by a magnet. The desorption of Cr(VI)-adsorbed MNPLB was found to be more than 93.72% with spent MNPLB depicting eleven successive adsorption-desorption cycles. Copyright © 2016. Published by Elsevier B.V.

  8. Papaya Seeds as A Low-Cost Sorbent for Removing Cr(VI) from The Aqueous Solution

    Science.gov (United States)

    Rahmawati, Atik; Marwoto, Putut; Karunia Z, Anita

    2016-08-01

    The presence of chromium (VI) contaminants and their toxicity in aqueous streams important environmental problems. Adsorption is one of the effective techniques that can be used for removing metal from wastewater. This research was initiated by preparing sorbent from papaya seeds and determining its functional group contents by using FT-IR. The adsorption process was carried out in a batch method. The study of adsorption aspects involved the pH, initial Cr (VI) concentration and contact time between Cr (VI) and sorbent. FT IR analysis results showed that the main functional groups are carbonyl, hydroxyl, and carboxylic. It was also found that the effective pH for Cr (VI) uptake is 2.0 and increasing contact time would increase the Cr (VI) uptake. In addition, the equilibrium was reached after 40 minutes interaction and the increase of initial chromium (VI) concentration would increase the sorbent uptake percentage. All these results indicated that papaya seed is a potential sorbent for removing Cr (VI) from aqueous solutions.

  9. A study on the dissolution rates of K-Cr(VI)-jarosites: kinetic analysis and implications.

    Science.gov (United States)

    Reyes, Iván A; Mireles, Ister; Patiño, Francisco; Pandiyan, Thangarasu; Flores, Mizraim U; Palacios, Elia G; Gutiérrez, Emmanuel J; Reyes, Martín

    2016-01-01

    The presence of natural and industrial jarosite type-compounds in the environment could have important implications in the mobility of potentially toxic elements such as lead, mercury, arsenic, chromium, among others. Understanding the dissolution reactions of jarosite-type compounds is notably important for an environmental assessment (for water and soil), since some of these elements could either return to the environment or work as temporary deposits of these species, thus would reduce their immediate environmental impact. This work reports the effects of temperature, pH, particle diameter and Cr(VI) content on the initial dissolution rates of K-Cr(VI)-jarosites (KFe3[(SO4)2 - X(CrO4)X](OH)6). Temperature (T) was the variable with the strongest effect, followed by pH in acid/alkaline medium (H3O(+)/OH(-)). It was found that the substitution of CrO4 (2-)in Y-site and the substitution of H3O(+) in M-site do not modify the dissolution rates. The model that describes the dissolution process is the unreacted core kinetic model, with the chemical reaction on the unreacted core surface. The dissolution in acid medium was congruent, while in alkaline media was incongruent. In both reaction media, there is a release of K(+), SO4 (2-) and CrO4 (2-) from the KFe3[(SO4)2 - X(CrO4)X](OH)6 structure, although the latter is rapidly absorbed by the solid residues of Fe(OH)3 in alkaline medium dissolutions. The dissolution of KFe3[(SO4)2 - X(CrO4)X](OH)6 exhibited good stability in a wide range of pH and T conditions corresponding to the calculated parameters of reaction order n, activation energy E A and dissolution rate constants for each kinetic stages of induction and progressive conversion. The kinetic analysis related to the reaction orders and calculated activation energies confirmed that extreme pH and T conditions are necessary to obtain considerably high dissolution rates. Extreme pH conditions (acidic or alkaline) cause the preferential release of K(+), SO4 (2

  10. Optimization of production of extracellular polymeric substances by Arthrobacter viscosus and their interaction with a 13X zeolite for the biosorption of Cr(VI).

    Science.gov (United States)

    Quintelas, Cristina; da Silva, Vítor B; Silva, Bruna; Figueiredo, Hugo; Tavares, Teresa

    2011-10-01

    In this work we aimed to optimize the production of extracellular polymeric substances (EPS) by an Arthrobacter viscosus biofilm supported on 13X zeolite to be used in the biosorption of Cr(VI). The optimization parameters were agitation rate, work volume, pH and glucose concentration. Following the optimization of EPS production, the biofilm was used in the biosorption of hexavalent Cr from liquid solutions. Differences between the use of dead or active biomass and between the performance of zeolite in powder or in pellet form were also studied. The optimized EPS production allowed values of metal uptake between 2.72 mg/g(biosorbent) and 7.88 mg/g(biosorbent) for initial Cr(VI) concentrations of 20-60 mg/L. For an initial concentration of 20 mg/L, the optimal conditions of EPS production allowed an increase of 10% on the removal percentage of total Cr, and the use of zeolite as a powder rather than the pelleted form produced an increase of 46.5% in the removal percentage. For the initial concentration of 60 mg/L, the use of active biomass compared to dried biomass allowed a reduction of the time required for the total removal of Cr(VI) from 20 to 13 days.

  11. Removal of Cr(VI from Water Using a New Reactive Material: Magnesium Oxide Supported Nanoscale Zero-Valent Iron

    Directory of Open Access Journals (Sweden)

    Alessio Siciliano

    2016-08-01

    Full Text Available The chromium pollution of water is an important environmental and health issue. Cr(VI removal by means of metallic iron is an attractive method. Specifically, nanoscopic zero valent iron (NZVI shows great reactivity, however, its applicability needs to be further investigated. In the present paper, NZVI was supported on MgO grains to facilitate the treatments for remediation of chromium-contaminated waters. The performances and mechanisms of the developed composite, in the removal of hexavalent chromium, were investigated by means of batch and continuous tests. Kinetic studies, under different operating conditions, showed that reduction of Cr(VI could be expressed by a pseudo second-order reaction kinetic. The reaction rate increased with the square of Fe(0 amount, while it was inversely proportional to the initial chromium concentration. The process performance was satisfactory also under uncontrolled pH, and a limited influence of temperature was observed. The reactive material was efficiently reusable for many cycles without any regeneration treatment. The performances in continuous tests were close to 97% for about 80 pore volume of reactive material.

  12. Chromium (VI) reduction in acetate- and molasses-amended natural media: empirical model development

    Energy Technology Data Exchange (ETDEWEB)

    Hansen, Scott [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Boukhalfa, Hakim [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Karra, Satish [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Wang, Dongping [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Vesselinov, Velimir Valentinov [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2017-11-21

    Stimulating indigenous microbes to reduce heavy metals from highly toxic oxidized species to more benign reduced species is a promising groundwater remediation technique that has already seen successful field applications. Designing such a bio-remediation scheme requires a model incorporating the kinetics of nonlinear bio-geochemical interactions between multiple species. With this motivation, we performed a set of microcosm experiments in natural sediments and their indigenous pore water and microbes, generating simultaneous time series for concentrations of Cr(VI), an electron donor (both molasses and acetate were considered), and biomass. Molasses was found to undergo a rapid direct abiotic reaction which eliminated all Cr(VI) before any biomass had time to grow. This was not found in the acetate microcosms, and a distinct zero-order bio-reduction process was observed. Existing models were found inappropriate and a new set of three coupled governing equations representing these process dynamics were developed and their parameters calibrated against the time series from the acetate-amended microcosms. Cell suspension batch experiments were also performed to calibrate bio-reduction rates in the absence of electron donor and sediment. The donor used to initially grow the cells (molasses or acetate) was found not to impact the reduction rate constants in suspension, which were orders of magnitude larger than those explaining the natural media microcosm experiments. This suggests the limited utility of kinetics determined in suspension for remedial design. Scoping studies on the natural media microcosms were also performed, suggesting limited impact of foreign abiotic material and minimal effect of diffusion limitation in the vertical dimension. These analyses may be of independent value to future researchers.

  13. Electrothermal atomic absorption spectrometric determination of Cr(VI) during ferrochrome production

    Energy Technology Data Exchange (ETDEWEB)

    Mandiwana, Khakhathi L. [Department of Chemistry, Tshwane University of Technology, Private Bag X31, Rosslyn 0200 (South Africa)]. E-mail: MandiwanaKL@tut.ac.za; Panichev, Nikolay [Department of Chemistry, Tshwane University of Technology, Private Bag X31, Rosslyn 0200 (South Africa); Ngobeni, Prince [Department of Chemistry, Tshwane University of Technology, Private Bag X31, Rosslyn 0200 (South Africa)

    2007-07-16

    The level of the generation of hexavalent chromium during ferrochrome production was checked. The concentration of Cr(VI) increases with each stage of ferrochrome production, 7070 {mu}g g{sup -1} being the highest concentration encountered in the last stage of production (dust). This concentration exceeds the maximum acceptable total Cr concentration per 8 h by a factor of more than 1000. It was further observed that there is a higher contamination of soil by this pollutant closer to the plant than further away. The highest concentrations of Cr(VI) in soil and grass were found to be 12.7 and 4.2 {mu}g g{sup -1}, respectively. The results of the investigation indicate that the consumption of such grass by animals do not pose any health hazard, for concentrations of the toxic Cr species are very low. Therefore, the release of emissions, including dust, during ferrochrome production, is a major contributor to occupational diseases and death to people working in ferrochrome production plant or mine.

  14. Higher adsorption capacity of Spirulina platensis alga for Cr(VI) ions removal: parameter optimisation, equilibrium, kinetic and thermodynamic predictions.

    Science.gov (United States)

    Gunasundari, Elumalai; Senthil Kumar, Ponnusamy

    2017-04-01

    This study discusses about the biosorption of Cr(VI) ion from aqueous solution using ultrasonic assisted Spirulina platensis (UASP). The prepared UASP biosorbent was characterised by Fourier transform infrared spectroscopy, X-ray diffraction, Brunauer-Emmet-Teller, scanning electron spectroscopy and energy dispersive X-ray and thermogravimetric analyses. The optimum condition for the maximum removal of Cr(VI) ions for an initial concentration of 50 mg/l by UASP was measured as: adsorbent dose of 1 g/l, pH of 3.0, contact time of 30 min and temperature of 303 K. Adsorption isotherm, kinetics and thermodynamic parameters were calculated. Freundlich model provided the best results for the removal of Cr(VI) ions by UASP. The adsorption kinetics of Cr(VI) ions onto UASP showed that the pseudo-first-order model was well in line with the experimental data. In the thermodynamic study, the parameters like Gibb's free energy, enthalpy and entropy changes were evaluated. This result explains that the adsorption of Cr(VI) ions onto the UASP was exothermic and spontaneous in nature. Desorption of the biosorbent was done using different desorbing agents in which NaOH gave the best result. The prepared material showed higher affinity for the removal of Cr(VI) ions and this may be an alternative material to the existing commercial adsorbents.

  15. Well-Dispersed Nanoscale Zero-Valent Iron Supported in Macroporous Silica Foams: Synthesis, Characterization, and Performance in Cr(VI Removal

    Directory of Open Access Journals (Sweden)

    Chaoxia Zhao

    2017-01-01

    Full Text Available Well-dispersed nanoscale zero-valent iron (NZVI supported inside the pores of macroporous silica foams (MOSF composites (Mx-NZVI has been prepared as the Cr(VI adsorbent by simply impregnating the MOSF matrix with ferric chloride, followed by the chemical reduction with NaHB4 in aqueous solution at ambient atmosphere. Through the support of MOSF, the reactivity and stability of NZVI are greatly improved. Transmission electron microscopy (TEM results show that NZVI particles are spatially well-dispersed with a typical core-shell structure and supported inside MOSF matrix. The N2 adsorption-desorption isotherms demonstrate that the Mx-NZVI composites can maintain the macroporous structure of MOSF and exhibit a considerable high surface area (503 m2·g−1. X-ray photoelectron spectroscopy (XPS and powder X-ray diffraction (XRD measurements confirm the core-shell structure of iron nanoparticles composed of a metallic Fe0 core and an Fe(II/Fe(III species shell. Batch experiments reveal that the removal efficiency of Cr(VI can reach 100% when the solution contains 15.0 mg·L−1 of Cr(VI at room temperature. In addition, the solution pH and the composites dosage can affect the removal efficiency of Cr(VI. The Langmuir isotherm is applicable to describe the removal process. The kinetic studies demonstrate that the removal of Cr(VI is consistent with pseudo-second-order kinetic model.

  16. A Cr(VI) selective probe based on a quinoline-amide calix[4]arene

    Science.gov (United States)

    Ferreira, Juliane F.; Bagatin, Izilda A.

    2018-01-01

    A new quinoline-amide calix[4]arene 3-receptor for detection of hazardous anions and cations have been synthesized. The 3-receptor was examined for its sensing properties towards several different anions (Cr2O72 -, SCN-, F-, Cl-, NO3-) and metal ions (Hg2+, Cd2+, Ag+) by UV-vis and fluorescence spectroscopies. It was detected that the 3-receptor has only sensing ability for Cr2O72 - and Hg2+ ions, resulting in the association constants higher for Cr2O72 - than to the Hg2+ ions. High selectivity towards Cr2O72 - were also observed by fluorescence measurement among other ions (F-, Cl-, SCN-, Hg2+, Cd2+, Ag+) with a low limit of detection (7.36 × 10-6 mol dm-3). Proton NMR anion-binding investigations revealed a strong interaction of Cr2O72 - anion with NH and CH groups of the receptor, showing that the combination with hydrogen-bonds donor groups strengthened the anion receptor association. Furthermore, remarkable association constants for dichromate anion obtained by all techniques strongly suggest the 3-receptor as a selective Cr(VI) sensor.

  17. Simultaneous removal of Cr(VI) and phenol contaminants using Z-scheme bismuth oxyiodide/reduced graphene oxide/bismuth sulfide system under visible-light irradiation.

    Science.gov (United States)

    Chen, Acong; Bian, Zhaoyong; Xu, Jie; Xin, Xin; Wang, Hui

    2017-12-01

    An all-solid-state Z-scheme system containing Bi-based semiconductors bismuth oxyiodide (BiOI) and bismuth sulfide (Bi 2 S 3 ) was constructed on reduced graphene oxide (rGO) sheets through an electrostatic self-assembly method to simultaneously remove aqueous Cr(VI) and phenol. In this Z-scheme that mimicked natural photosynthesis, photoinduced electrons in the conduction band (CB) of BiOI were transferred through rGO and reacted with photoinduced holes in the valence band (VB) of Bi 2 S 3 , which significantly increased its photocatalytic activity. The reduction and oxidation reactions were performed on Bi 2 S 3 and BiOI photocatalysts, respectively. Furthermore, complex contaminants of coexisting heavy metal Cr(VI) and organic phenol were treated using the system under visible-light irradiation. Results showed that Cr(VI) reduction and phenol oxidation were achieved efficiently with optimum reductive and oxidative efficiencies up to 73% and 95% under visible-light irradiation, respectively. This work provided a promising method of simultaneously removing heavy metals and organic pollutants by using a Z-scheme system with enhanced photocatalytic activity. Copyright © 2017 Elsevier Ltd. All rights reserved.

  18. Visible-light-driven g-C3N4/Ti3+-TiO2 photocatalyst co-exposed {0 0 1} and {1 0 1} facets and its enhanced photocatalytic activities for organic pollutant degradation and Cr(VI) reduction

    Science.gov (United States)

    Lu, Dan; Zhang, Gaoke; Wan, Zhen

    2015-12-01

    Novel g-C3N4/Ti3+-TiO2 photocatalyst co-exposed {0 0 1} and {1 0 1} facets of TiO2 was synthesized via a hydrothermal-sonication assisted strategy. The photocatalytic activities of the as-obtained photocatalyst were evaluated by the degradation of rhodamine B (RhB) and the reduction of Cr(VI) under visible-light irradiation. It was found that the g-C3N4/Ti3+-TiO2 composites with 6 wt% g-C3N4 exhibited the highest visible-light photocatalytic efficiency, which is also higher than the pure g-C3N4 and Ti3+-TiO2. A possible photocatalytic mechanism was discussed on the basis of the theoretical analyses and scavenger experiments. Results show that holes (h+) and superoxide anions (rad O2-) reactive species participated in the degradation of RhB solution over the g-C3N4/Ti3+-TiO2 composites. The enhanced photocatalytic activities of g-C3N4/Ti3+-TiO2 composites can be attributed to the wide optical adsorption of g-C3N4 and Ti3+ as well as the effectively separation and transportation of photo-generated electrons and holes pairs, which was resulted from the surface heterojunction between the g-C3N4 and Ti3+-TiO2 nanosheets co-exposed {1 0 1} and {0 0 1} facets of anatase TiO2.

  19. Biosorption of Cr(VI) and As(V) at high concentrations by organic and inorganic wastes

    Science.gov (United States)

    María Rivas Pérez, Ivana; Paradelo Núñez, Remigio; Nóvoa Muñoz, Juan Carlos; Arias Estévez, Manuel; José Fernández Sanjurjo, María; Álvarez Rodríguez, Esperanza; Núñez Delgado, Avelino

    2016-04-01

    The potential reutilization of several wastes as biosorbents for As(V) and Cr(VI) has been assessed in batch-type experiments. The materials studied were one inorganic: mussel shell, and three organic: pine bark, oak ash and hemp waste. Batch experiments were performed in order to determine the removal capacity of the wastes under conditions of high As(V) and Cr(VI) loads. For this, 3 g of each waste material were added with 30 mL NaNO3 0.01 M dissolutions containing 0, 0.5, 1.5, 3 and 6 mmol As(V) L-1 or Cr(VI) L-1, prepared from analytical grade Na2HAsO4 or K2Cr2O7. The resulting suspensions were shaken for 24 h, centrifuged and filtered. Once each batch experiment corresponding to the sorption trials ended, each individual sample was added with 30 mL of NaNO3 0.01 M to desorb As(V) or Cr(VI), shaken for 24 h, centrifuged and filtered as in the sorption trials. Oak ash showed high sorption (>76%) and low desorption (hemp waste (98%) with very low desorption (hemp waste and mussel shell, that presented very low Cr(VI) sorption (<10%). Sorption data for both elements were better described by the Freundlich than by the Langmuir model. The variable results obtained for the removal of the two anionic contaminants for a given sorbent suggest that different mechanisms govern removal from the solution in each case. In summary, oak ash would be an efficient sorbent material for As(V), but not for Cr(VI), while pine bark would be the best sorbent for Cr(VI) removal.

  20. Site-specific functionalization for chemical speciation of Cr(III) and Cr(VI) using polyaniline impregnated nanocellulose composite: equilibrium, kinetic, and thermodynamic modeling

    Science.gov (United States)

    Jain, Priyanka; Varshney, Shilpa; Srivastava, Shalini

    2017-07-01

    Site-specific functionalizations are the emergent attention for the enhancement of sorption latent of heavy metals. Limited chemistry has been applied for the fabrication of diafunctionalized materials having potential to tether both environmentally stable oxidation states of chromium (Cr(III) and Cr(VI). Polyaniline impregnated nanocellulose composite (PANI-NCC) has been fabricated using click chemistry and explored for the removal of Cr(III) and Cr(VI) from hydrological environment. The structure, stability, morphology, particle size, surface area, hydrophilicity, and porosity of fabricated PANI-NCC were characterized comprehensively using analytical techniques and mathematical tools. The maximum sorption performance of PANI-NCC was procured for (Cr(III): 47.06 mg g-1; 94.12 %) and (Cr(VI): 48.92 mg g-1; 97.84 %) by equilibrating 0.5 g sorbent dose with 1000 mL of 25 mg L-1 chromium conc. at pH 6.5 and 2.5 for Cr(III) and Cr(VI), respectively. The sorption data showed a best fit to the Langmuir isotherm and pseudo-second-order kinetic model. The negative value of ∆ G° (-8.59 and -11.16 kJ mol-1) and ∆ H° (66.46 × 10-1 and 17.84 × 10-1 kJ mol-1), and positive value of ∆ S° (26.66 and 31.46 J mol-1K-1) for Cr(III) and Cr(VI), respectively, reflect the spontaneous, feasibility, and exothermic nature of the sorption process. The application of fabricated PANI-NCC for removing both the forms of chromium in the presence of other heavy metals was also tested at laboratory and industrial waste water regime. These findings open up new avenues in the row of high performance, scalable, and economic nanobiomaterial for the remediation of both forms of chromium from water streams.

  1. Cr(VI) and Conductivity as Indicators of Surface Water Pollution from Ferrochrome Production in South Africa: Four Case Studies

    Science.gov (United States)

    Loock-Hattingh, M. M.; Beukes, J. P.; van Zyl, P. G.; Tiedt, L. R.

    2015-10-01

    South Africa is one of the largest ferrochromium (FeCr) producers. Most FeCr is exported to developed countries. Therefore the impact of this industry is of national and international importance. Cr(VI) and conductivity of surface water in four case study areas, near five FeCr smelters were monitored for approximately 1 year. Results indicated that FeCr production in three case study areas had a negative influence on the Cr(VI) concentration and/or the conductivity of surface waters. In the remaining case study areas, drinking water, originating from groundwater, was severely polluted with Cr(VI). The main factors causing pollution were surface run-off and/or seepage, while atmospheric deposition did not seem to contribute significantly. The extinction of diatoms during a severe Cr(VI) surface water pollution event (concentrations up to 216 µg/L) in one of the case study areas was also observed, which clearly indicates the ecological impact of such surface water pollution events.

  2. Isolation of a star-shaped uranium(V/VI) cluster from the anaerobic photochemical reduction of uranyl(VI)

    Energy Technology Data Exchange (ETDEWEB)

    Chatelain, Lucile; White, Sarah; Scopelliti, Rosario; Mazzanti, Marinella [Ecole Polytechnique Federale de Lausanne (EPFL) (Switzerland). Inst. de Sciences et Ingenierie Chimiques

    2016-11-07

    Actinide oxo clusters are an important class of compounds due to their impact on actinide migration in the environment. The photolytic reduction of uranyl(VI) has potential application in catalysis and spent nuclear fuel reprocessing, but the intermediate species involved in this reduction have not yet been elucidated. Here we show that the photolysis of partially hydrated uranyl(VI) in anaerobic conditions leads to the reduction of uranyl(VI), and to the incorporation of the resulting U{sup V} species into the stable mixed-valent star-shaped U{sup VI}/U{sup V} oxo cluster [U(UO{sub 2}){sub 5}(μ{sub 3}-O){sub 5}(PhCOO){sub 5}(Py){sub 7}]. This cluster is only the second example of a U{sup VI}/U{sup V} cluster and the first one associating uranyl groups to a non-uranyl(V) center. The U{sup V} center in 1 is stable, while the reaction of uranyl(V) iodide with potassium benzoate leads to immediate disproportionation and formation of the U{sub 12}{sup IV}U{sub 4}{sup V}O{sub 24} cluster {[K(Py)_2]_2[K(Py)]_2[U_1_6O_2_4(PhCOO)_2_4(Py)_2]}.

  3. One-pot synthesis of Mn-doped TiO{sub 2} grown on graphene and the mechanism for removal of Cr(VI) and Cr(III)

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Zengping; Li, Yaru; Guo, Meng; Xu, Fengyun; Wang, Peng [School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Du, Yu [China Tobacco Yunnan Industrial Co., Ltd., Yunnan 651600 (China); Na, Ping, E-mail: naping@tju.edu.cn [School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China)

    2016-06-05

    Highlights: • rGO-Mn-TiO{sub 2} is synthesized through one-pot hydrothermal method. • Cr(total) removal effectiveness reaches to 97.32% in 30 min under visible light, as the initial concentration of Cr(VI) is 20 mg/L. • Mn-TiO{sub 2} and rGO synergistically contribute to the adsorption and photocatalytic reduction of Cr. • Cr(III) being adsorbed by rGO helps to the release of abundant photocatalytic sites of Mn-TiO{sub 2}. - Abstract: Mn-doped TiO{sub 2} grown on reduced graphene oxide(rGO) was synthesized by one-pot hydrothermal method and the photocatalytic removal of Cr by the material was investigated under sunlight. The materials were characterized by a combination of scanning electron microscopy, transmission electron microscopy, X-ray diffraction, thermogravimetric analysis, Brunauer-Emmett-Teller method, UV–vis diffuse reflectance spectra, photoluminescence spectra, electrochemical impedance spectroscopy and X-ray photoelectron spectroscopy. Cr(total) removal efficiency of the material is 97.32% in 30 min and 99.02% in 60 min under sunlight irradiation, as the initial concentration of Cr(VI) is 20 mg/L. The high photocatalytic activity under visible light is considered mainly due to the Mn-doping, and rGO plays an important role in the synergetic effect of adsorption and photocatalysis to sustain the high efficient removal of Cr(VI) and Cr(III). Cr(VI) adsorbed on the surface of rGO is reduced to Cr(III) by photo electrons which are transported through rGO, and the reaction product Cr(III) continues to be adsorbed. The process contributes to the release of abundant photocatalytic sites of Mn-TiO{sub 2} and improves photocatalytic efficiency. The excellent adsorption and photocatalytic effect with the explanation of the synergetic mechanism are very useful not only for fundamental research but also for the potential practical applications.

  4. Polyurethane-Keratin Membranes: Structural Changes by Isocyanate and pH, and the Repercussion on Cr(VI Removal

    Directory of Open Access Journals (Sweden)

    María D. Manrique-Juárez

    2013-01-01

    Full Text Available Keratin has the capacity to interact with metal ions. In order to take advantage of this potential, a novel membrane with polyurethane and keratin has been developed and studied for removal of Cr(VI from aqueous solution. Physicochemical and morphological properties of these hybrid membranes were studied, varying synthesis parameters such as the type of isocyanate and pH in keratin solution. The effects of using diphenyl-methane-diisocyanate or toluene-diisocyanate and modifying the pH in keratin solutions were evaluated by scanning electron microscopy, Fourier transform infrared spectroscopy, and dynamical mechanical analysis. Results show that pH has a strong influence on morphology and on Cr(VI removal efficiency. When pH in keratin solution is low (2.5, the protein separates from water, and a more closed cell in the membrane is obtained affecting its mechanical properties. The removal efficiency of Cr(VI was also assessed at different pH values of chromium solutions. These results show that when pH of the Cr solution is acidic (at 1.5, the Cr(VI removal percentages increase significantly, reaching up to a 58%. Thus this paper demonstrates the successful combination of synthetic and natural polymers depending on the process parameters to be applied in the critical purpose of remediation of Cr(VI contamination.

  5. The influence of Chromium supplied by tanning and wet finishing processes on the formation of cr(vi in leather

    Directory of Open Access Journals (Sweden)

    W. F. Fuck

    2011-06-01

    Full Text Available Chromium used in leather manufacturing can be oxidized from the trivalent to the hexavalent state, causing environmental concerns. In this study, the influence of Cr(III from tanning, deacidification pH, fatliquors, chrome retanning and vegetable retanning on the formation of Cr(VI in leather was analyzed by comparing natural and aged samples. In wet-blue leather, even after aging and in fatliquored leathers that did not suffer the aging process, the presence of Cr(VI was always below the detection limit of 3 mg/kg. Considering the presence of Cr(VI, the supply of chromium during the retanning step had a more significant effect than during the tanning. In the fatliquoring process with sulfites, fish and synthetic fatliquor leather samples contained Cr(VI when aged, and the highest concentration detected was 26.7 mg/kg. The evaluation of Cr(VI formation led to recommendations for regulation in the leather industry.

  6. ZnO-PLLA nanofiber nanocomposite for continuous flow mode purification of water from Cr(VI).

    Science.gov (United States)

    Burks, T; Akthar, F; Saleemi, M; Avila, M; Kiros, Y

    2015-01-01

    Nanomaterials of ZnO-PLLA nanofibers have been used for the adsorption of Cr(VI) as a prime step for the purification of water. The fabrication and application of the flexible ZnO-PLLA nanofiber nanocomposite as functional materials in this well-developed architecture have been achieved by growing ZnO nanorod arrays by chemical bath deposition on synthesized electrospun poly-L-lactide nanofibers. The nanocomposite material has been tested for the removal and regeneration of Cr(IV) in aqueous solution under a "continuous flow mode" by studying the effects of pH, contact time, and desorption steps. The adsorption of Cr(VI) species in solution was greatly dependent upon pH. SEM micrographs confirmed the successful fabrication of the ZnO-PLLA nanofiber nanocomposite. The adsorption and desorption of Cr(VI) species were more likely due to the electrostatic interaction between ZnO and Cr(VI) ions as a function of pH. The adsorption and desorption experiments utilizing the ZnO-PLLA nanofiber nanocomposite have appeared to be an effective nanocomposite in the removal and regeneration of Cr(VI) species.

  7. ZnO-PLLA Nanofiber Nanocomposite for Continuous Flow Mode Purification of Water from Cr(VI

    Directory of Open Access Journals (Sweden)

    T. Burks

    2015-01-01

    Full Text Available Nanomaterials of ZnO-PLLA nanofibers have been used for the adsorption of Cr(VI as a prime step for the purification of water. The fabrication and application of the flexible ZnO-PLLA nanofiber nanocomposite as functional materials in this well-developed architecture have been achieved by growing ZnO nanorod arrays by chemical bath deposition on synthesized electrospun poly-L-lactide nanofibers. The nanocomposite material has been tested for the removal and regeneration of Cr(IV in aqueous solution under a “continuous flow mode” by studying the effects of pH, contact time, and desorption steps. The adsorption of Cr(VI species in solution was greatly dependent upon pH. SEM micrographs confirmed the successful fabrication of the ZnO-PLLA nanofiber nanocomposite. The adsorption and desorption of Cr(VI species were more likely due to the electrostatic interaction between ZnO and Cr(VI ions as a function of pH. The adsorption and desorption experiments utilizing the ZnO-PLLA nanofiber nanocomposite have appeared to be an effective nanocomposite in the removal and regeneration of Cr(VI species.

  8. Visible-light-driven g-C{sub 3}N{sub 4}/Ti{sup 3+}-TiO{sub 2} photocatalyst co-exposed {0 0 1} and {1 0 1} facets and its enhanced photocatalytic activities for organic pollutant degradation and Cr(VI) reduction

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Dan; Zhang, Gaoke, E-mail: gkzhang@whut.edu.cn; Wan, Zhen

    2015-12-15

    Graphical abstract: Schematic illustration for the mechanism of photo-generated charge carrier transfers in g-C{sub 3}N{sub 4}/Ti{sup 3+}-TiO{sub 2} photocatalyst and its visible-light photocatalytic performance. - Highlights: • g-C{sub 3}N{sub 4}/Ti{sup 3+}-TiO{sub 2} composite co-exposed {0 0 1} and {1 0 1} facets of TiO{sub 2} was synthesized. • RhB and Cr(VI) aqueous solutions were used to evaluate the photocatalytic activities. • h{sup +} and ·O{sub 2}{sup −} are the critical reactive species in the degradation of RhB solution. • Surface heterojunction of co-exposed {1 0 1} and {0 0 1} facets improve the separation. - Abstract: Novel g-C{sub 3}N{sub 4/}Ti{sup 3+}-TiO{sub 2} photocatalyst co-exposed {0 0 1} and {1 0 1} facets of TiO{sub 2} was synthesized via a hydrothermal–sonication assisted strategy. The photocatalytic activities of the as-obtained photocatalyst were evaluated by the degradation of rhodamine B (RhB) and the reduction of Cr(VI) under visible-light irradiation. It was found that the g-C{sub 3}N{sub 4}/Ti{sup 3+}-TiO{sub 2} composites with 6 wt% g-C{sub 3}N{sub 4} exhibited the highest visible-light photocatalytic efficiency, which is also higher than the pure g-C{sub 3}N{sub 4} and Ti{sup 3+}-TiO{sub 2}. A possible photocatalytic mechanism was discussed on the basis of the theoretical analyses and scavenger experiments. Results show that holes (h{sup +}) and superoxide anions (·O{sub 2}{sup −}) reactive species participated in the degradation of RhB solution over the g-C{sub 3}N{sub 4}/Ti{sup 3+}-TiO{sub 2} composites. The enhanced photocatalytic activities of g-C{sub 3}N{sub 4}/Ti{sup 3+}-TiO{sub 2} composites can be attributed to the wide optical adsorption of g-C{sub 3}N{sub 4} and Ti{sup 3+} as well as the effectively separation and transportation of photo-generated electrons and holes pairs, which was resulted from the surface heterojunction between the g-C{sub 3}N{sub 4} and Ti{sup 3+}-TiO{sub 2} nanosheets co-exposed {1

  9. Characterization of the effect of Cr(VI) on humoral innate immunity using Drosophila melanogaster.

    Science.gov (United States)

    Pragya, P; Shukla, A K; Murthy, R C; Abdin, M Z; Kar Chowdhuri, D

    2015-11-01

    With the advancement of human race, different anthropogenic activities have heaped the environment with chemicals that can cause alteration in the immune system of exposed organism. As a first line of barrier, the evolutionary conserved innate immunity is crucial for the health of an organism. However, there is paucity of information regarding in vivo assessment of the effect of environmental chemicals on innate immunity. Therefore, we examined the effect of a widely used environmental chemical, Cr(VI), on humoral innate immune response using Drosophila melanogaster. The adverse effect of Cr(VI) on host humoral response was characterized by decreased gene expression of antimicrobial peptides (AMPs) in the exposed organism. Concurrently, a significantly decreased transcription of humoral pathway receptors (Toll and PGRP) and triglyceride level along with inhibition of antioxidant enzyme activities were observed in exposed organism. This in turn weakened the immune response of exposed organism that was manifested by their reduced resistance against bacterial infection. In addition, overexpression of the components of humoral immunity particularly Diptericin benefits Drosophila from Cr(VI)-induced humoral immune-suppressive effect. To our knowledge, this is the first report regarding negative impact of an environmental chemical on humoral innate immune response of Drosophila along with subsequent protection by AMPs, which may provide novel insight into host-chemical interactions. Also, our data validate the utility and sensitivity of Drosophila as a model that could be used for screening the possible risk of environmental chemicals on innate immunity with minimum ethical concern that can be further extrapolated to higher organisms. © 2014 Wiley Periodicals, Inc.

  10. Column study of enhanced Cr(VI) removal and longevity by coupled abiotic and biotic processes using Fe0 and mixed anaerobic culture

    DEFF Research Database (Denmark)

    Zhong, Jiawei; Yin, Weizhao; Li, Yongtao

    2017-01-01

    In this study, Fe(0) and mixed anaerobic culture were integrated in one column to investigate the coupled abiotic and biotic effects on hexa-valent chromium (Cr(VI)) removal and column longevity with an abiotic Fe(0) column in the control experiments. According to the breakthrough study, a slower...... by scanning electron microscopy (SEM), energy dispersive X-ray (EDX) and X-ray diffraction (XRD) confirmed that this enhancement was attributed to the higher consumption of iron and greater production of diverse reactive minerals (e.g., green rust, magnetite and lepidocrocite) induced by the synergistic...... interaction of Fe(0) and anaerobic culture, providing more reactive sites for Cr(VI) adsorption, reduction and co-precipitation. Furthermore, the decreasing breakthrough rates and growing iron corrosion along the biotic Fe(0) column demonstrated an inhomogeneous distribution of reactive zones in the column...

  11. Modifications to EPA Method 3060A to Improve Extraction of Cr(VI) from Chromium Ore Processing Residue-Contaminated Soils

    Science.gov (United States)

    Mills, Christopher T.; Bern, Carleton R.; Wolf, Ruth E.; Foster, Andrea L.; Morrison, Jean M.; Benzel, William M.

    2017-01-01

    It has been shown that EPA Method 3060A does not adequately extract Cr(VI) from chromium ore processing residue (COPR). We modified various parameters of EPA 3060A toward understanding the transformation of COPR minerals in the alkaline extraction and improving extraction of Cr(VI) from NIST SRM 2701, a standard COPR-contaminated soil. Aluminum and Si were the major elements dissolved from NIST 2701, and their concentrations in solution were correlated with Cr(VI). The extraction fluid leached additional Al and Si from the method-prescribed borosilicate glass vessels which appeared to suppress the release of Cr(VI). Use of polytetrafluoroethylene vessels and intensive grinding of NIST 2701 increased the amount of Cr(VI) extracted. These modifications, combined with an increased extraction fluid to sample ratio of ≥900 mL g–1 and 48-h extraction time resulted in a maximum release of 1274 ± 7 mg kg–1 Cr(VI). This is greater than the NIST 2701 certified value of 551 ± 35 mg kg–1 but less than 3050 mg kg–1 Cr(VI) previously estimated by X-ray absorption near edge structure spectroscopy. Some of the increased Cr(VI) may have resulted from oxidation of Cr(III) released from brownmillerite which rapidly transformed during the extractions. Layered-double hydroxides remained stable during extractions and represent a potential residence for unextracted Cr(VI).

  12. Modifications to EPA Method 3060A to Improve Extraction of Cr(VI) from Chromium Ore Processing Residue-Contaminated Soils.

    Science.gov (United States)

    Mills, Christopher T; Bern, Carleton R; Wolf, Ruth E; Foster, Andrea L; Morrison, Jean M; Benzel, William M

    2017-10-03

    It has been shown that EPA Method 3060A does not adequately extract Cr(VI) from chromium ore processing residue (COPR). We modified various parameters of EPA 3060A toward understanding the transformation of COPR minerals in the alkaline extraction and improving extraction of Cr(VI) from NIST SRM 2701, a standard COPR-contaminated soil. Aluminum and Si were the major elements dissolved from NIST 2701, and their concentrations in solution were correlated with Cr(VI). The extraction fluid leached additional Al and Si from the method-prescribed borosilicate glass vessels which appeared to suppress the release of Cr(VI). Use of polytetrafluoroethylene vessels and intensive grinding of NIST 2701 increased the amount of Cr(VI) extracted. These modifications, combined with an increased extraction fluid to sample ratio of ≥900 mL g(-1) and 48-h extraction time resulted in a maximum release of 1274 ± 7 mg kg(-1) Cr(VI). This is greater than the NIST 2701 certified value of 551 ± 35 mg kg(-1) but less than 3050 mg kg(-1) Cr(VI) previously estimated by X-ray absorption near edge structure spectroscopy. Some of the increased Cr(VI) may have resulted from oxidation of Cr(III) released from brownmillerite which rapidly transformed during the extractions. Layered-double hydroxides remained stable during extractions and represent a potential residence for unextracted Cr(VI).

  13. The Effect of Phosphatation and Granulation Zeolite in the Adsorption of Cr(VI

    Directory of Open Access Journals (Sweden)

    Sri Wardhani

    2017-09-01

    Full Text Available The purpose of this research to study effect of contact time on adsorption of Cr(VI ion using Granules Alumino Silico Phosphate (GASP and the effect of Cr (VI concentration on adsorption capacity at GASP. The GASF synthesis process is carried out in several main stages: 1 activation of zeolite with addition of HCl, 2 zeolite phosphatation with addition of NH4H2PO4 ratio Si/P = 1/6 at 235ᴼC for 5 hours, 3 how make GASP with addition of zeolite phosphate (Alumino Silicone Phosphate and chitosan gel with a syringe pump speed of 50 mL/min. GASP is characterized using XRF, FT-IR and SAA. The contact time effect is tested using 0.1 g of GASF in K2CrO4 100 mg/L with a contact time variation of 0.5; 1.0; 1.5; 2.0 and 2.5 hours. The concentration effect on adsorption capacity is tested out using 0.1 g of GASP in K2CrO4 with concentration variation 25, 50, 75, 100 and 150 mg / L for 2 hours (optimum contact time. The adsorption capacity can be determined using the Langmuir equation. XRF characterization results showed a decrease in SiO2 levels of 18.10% and Al2O3 by 2.2% after phosphatation process. FTIR characterization results indicate the presence of O-H, N-H and C-H chitosan on absorption bands 1-3. The success of the phosphatation process was evidenced by the shift of wave numbers to the lower regions in the bands 7, 9 and 12 the absorption of tetrahedral silica and alumina shifted to bands 8, 10 and 13 tetrahedral phosphate uptake in accordance with Hooke's law. The result of the research showed that the optimum contact time occurred in the adsorption process for 2 hours. The concentration variation was directly proportional to the increase of the adsorbed Cr (VI ion mass. The presence of phosphatation and chitosan addition process can increase the value of adsorption capacity by 48,077 mg / g.

  14. Experimental data on adsorption of Cr(VI) from aqueous solution using nanosized cellulose fibers obtained from rice husk.

    Science.gov (United States)

    Pourfadakari, Sudabeh; Jorfi, Sahand; Ahmadi, Mehdi; Takdastan, Afshin

    2017-12-01

    The aim of this study was to evaluate the efficiency of nano-sized cellulose obtained from rice husk for Cr(VI) adsorption. The effect of operational parameters including initial pH (3-10), contact time (0-120 min), adsorbent dosage (0.2-1.5 g/L), and initial Cr(VI) concentration (5-50 mg/L) were investigated according to one factor at time method. The results showed, in pH=6, contact time=100 min, adsorbent dose=1.5 g/L and 30 mg/L initial chromium concentration, the adsorption efficiency reached to 92.99%. Also Langmuir isotherm with (R2=0.998 at 303 °K) and pseudo-first-order kinetic model (R2=0.993) were the best models for describing the Cr(VI) adsorption reactions. The negative values of [Formula: see text] and positive value of [Formula: see text] showed that, the Cr(VI) adsorption on NCFs was endothermic and spontaneously process. Therefore, it can be concluded that the application this method is recommended for removing Cr(VI) from aqueous solutions.

  15. Effects of soluble and particulate Cr(VI) on genome-wide DNA methylation in human B lymphoblastoid cells.

    Science.gov (United States)

    Lou, Jianlin; Wang, Yu; Chen, Junqiang; Ju, Li; Yu, Min; Jiang, Zhaoqiang; Feng, Lingfang; Jin, Lingzhi; Zhang, Xing

    2015-10-01

    Several previous studies highlighted the potential epigenetic effects of Cr(VI), especially DNA methylation. However, few studies have compared the effects of Cr(VI) on DNA methylation profiles between soluble and particulate chromate in vitro. Accordingly, Illumina Infinium Human Methylation 450K BeadChip array was used to analyze DNA methylation profiles of human B lymphoblastoid cells exposed to potassium dichromate or lead chromate, and the cell viability was also studied. Array based DNA methylation analysis showed that the impacts of Cr(VI) on DNA methylation were limited, only about 40 differentially methylated CpG sites, with an overlap of 15CpG sites, were induced by both potassium dichromate and lead chromate. The results of mRNA expression showed that after Cr(VI) treatment, mRNA expression changes of four genes (TBL1Y, FZD5, IKZF2, and KIAA1949) were consistent with their DNA methylation alteration, but DNA methylation changes of other six genes did not correlate with mRNA expression. In conclusion, both of soluble and particulate Cr(VI) could induce a small amount of differentially methylated sites in human B lymphoblastoid cells, and the correlations between DNA methylation changes and mRNA expression varied between different genes. Copyright © 2015 Elsevier B.V. All rights reserved.

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

    Directory of Open Access Journals (Sweden)

    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.

  17. Evaluation of the bioremoval of Cr(VI) and TOC in biofilters under continuous operation using response surface methodology.

    Science.gov (United States)

    Leles, Daniela M A; Lemos, Diego A; Filho, Ubirajara C; Romanielo, Lucienne L; de Resende, Miriam M; Cardoso, Vicelma L

    2012-06-01

    In the present study, the bioremoval of Cr(VI) and the removal of total organic carbon (TOC) were achieved with a system composed by an anaerobic filter and a submerged biofilter with intermittent aeration using a mixed culture of microorganisms originating from contaminated sludge. In the aforementioned biofilters, the concentrations of chromium, carbon, and nitrogen were optimized according to response surface methodology. The initial concentration of Cr(VI) was 137.35 mg l(-1), and a bioremoval of 85.23% was attained. The optimal conditions for the removal of TOC were 4 to 8 g l(-1) of sodium acetate, >0.8 g l(-1) of ammonium chloride and 60 to 100 mg l(-1) of Cr(VI). The results revealed that ammonium chloride had the strongest effect on the TOC removal, and 120 mg l(-1) of Cr(VI) could be removed after 156 h of operation. Moreover, 100% of the Cr(VI) and the total chromium content of the aerobic reactor output were removed, and TOC removals of 80 and 87% were attained after operating the anaerobic and aerobic reactors for 130 and 142 h, respectively. The concentrations of cells in both reactors remained nearly constant over time. The residence time distribution was obtained to evaluate the flow through the bioreactors.

  18. Synthesis of Poly(Ortho-Phenylenediamine Fluffy Microspheres and Application for the Removal of Cr(VI

    Directory of Open Access Journals (Sweden)

    Zhoufeng Wang

    2012-01-01

    Full Text Available We reported the synthesis of fluffy poly(o-phenylenediamine (PoPD microspheres via chemical polymerization of oPD monomers by ammonium persulfate (APS at room temperature. The SEM images showed that PoPD microspheres with an average diameter of 1.5 μm and their surfaces consist of highly oriented nanofibers. Furthermore, PoPD microspheres were used as adsorbent materials for the removal of Cr(VI from aqueous solutions. The Cr(VI adsorption behavior on the prepared PoPD microspheres was studied at different adsorption contact times, solution pH values, and amount of the adsorbent. Experimental isotherms of Cr(VI ions were successfully fit to the Langmuir isotherm model. The results indicate that the PoPD fluffy microspheres are an effective adsorbent for the removal of Cr(VI ions from aqueous solutions, and they could be useful in treatment of Cr(VI-polluted wastewaters.

  19. PROFIL LOGAM BERAT Cd, Cr (VI DAN Pb PADA LOKASI BERBEDA DI PROVINSI LAMPUNG SERTA BIOAKUMULASINYA PADA TANAMAN PANGAN

    Directory of Open Access Journals (Sweden)

    Hening Widowati

    2015-11-01

    Full Text Available The heavy metal profile analysis of Cd, Cr(VI and Pb in the different location in Lampung Province and their bioaccumulation to crops has been conducted. The aims were finding out the difference of metal accumulation in the different pollutant area and determining how it happened to the vegetables surrounding, which were kangkoong and spinach. The research methods were purposive sampling in the different location in Lampung Province, namely 1 highlands, 2 paddy fields, 3 road sides and 4industrial areas. Based on the results, it is found that the highest metal concentration of Cd, Cr(VI and Pb are in the industrial area. Commonly, the value of BCFo-w (0,12-2,00 is higher than BCF¬o-s (0,01-0,18 which shows that there is low metal accumulation of Cd, Cr(VI and Pb in kangkoong and spinach. Furthermore, the BCF value of Cd and Cr(VI are higher compared to Pb.  Keywords: Logam berat, Cd, Cr(VI, Pb,bioakumulasi.

  20. Comparative and competitive adsorption of Cr(VI), As(III), and Ni(II) onto coconut charcoal.

    Science.gov (United States)

    Wu, Yunhai; Wen, Yajun; Zhou, Jianxin; Cao, Julin; Jin, Yanping; Wu, Yunying

    2013-04-01

    This study evaluates the behavior of coconut charcoal (AC) to adsorb Cr(VI), As(III), and Ni(II) in mono- and multicomponent (binary and ternary) systems. Batch experiments were carried out for mono- and multicomponent systems with varying metal ion concentrations to investigate the competitive adsorption characteristics. The adsorption kinetics followed the mechanism of the pseudo-second-order equation in both single and binary systems, indicating chemical sorption as the rate-limiting step of adsorption mechanism. Equilibrium studies showed that the adsorption of Cr(VI), As(III), and Ni(II) followed the Langmuir model and maximum adsorption capacities were found to be 5.257, 0.042, and 1.748 mg/g, respectively. In multicomponent system, As(III) and Ni(II) adsorption competed intensely, while Cr(VI) adsorption was much less affected by competition than As(III) and Ni(II). With the presence of Cr(VI), the adsorption capacities of As(III) and Ni(II) on AC were higher than those in single system and the metal sorption followed the order of Ni(II) > As(III) > Cr(VI). The results from the sequential adsorption-desorption cycles showed that AC adsorbent held good desorption and reusability.

  1. Modacrylic anion-exchange fibers for Cr(VI) removal from chromium-plating rinse water in batch and flow-through column experiments.

    Science.gov (United States)

    Lee, Seung-Chan; Kang, Jin-Kyu; Sim, Eun-Hye; Choi, Nag-Choul; Kim, Song-Bae

    2017-11-10

    The aim of this study was to investigate Cr(VI) removal from chromium-plating rinse water using modacrylic anion-exchange fibers (KaracaronTM KC31). Batch experiments were performed with synthetic Cr(VI) solutions to characterize the KC31 fibers in Cr(VI) removal. Cr(VI) removal by the fibers was affected by solution pH; the Cr(VI) removal capacity was the highest at pH 2 and decreased gradually with a pH increase from 2 to 12. In regeneration and reuse experiments, the Cr(VI) removal capacity remained above 37.0 mg g(-1) over five adsorption-desorption cycles, demonstrating that the fibers could be successfully regenerated with NaCl solution and reused. The maximum Cr(VI) removal capacity was determined to be 250.3 mg g(-1) from the Langmuir model. In Fourier-transform infrared spectra, a Cr = O peak newly appeared at 897 cm(-1) after Cr(VI) removal, whereas a Cr-O peak was detected at 772 cm(-1) due to the association of Cr(VI) ions with ion-exchange sites. X-ray photoelectron spectroscopy analyses demonstrated that Cr(VI) was partially reduced to Cr(III) after the ion exchange on the surfaces of the fibers. Batch experiments with chromium-plating rinse water (Cr(VI) concentration = 1178.8 mg L(-1)) showed that the fibers had a Cr(VI) removal capacity of 28.1-186.4 mg g(-1) under the given conditions (fiber dose = 1-10 g L(-1)). Column experiments (column length = 10 cm, inner diameter = 2.5 cm) were conducted to examine Cr(VI) removal from chromium-plating rinse water by the fibers under flow-through column conditions. The Cr(VI) removal capacities for the fibers at flow rates of 0.5 and 1.0 mL min(-1) were 214.8 and 171.5 mg g(-1), respectively. This study demonstrates that KC31 fibers are effective in the removal of Cr(VI) ions from chromium-plating rinse water.

  2. Photoredox degradation of different water pollutants (MO, RhB, MB, and Cr(VI)) using Fe–N–S-tri-doped TiO{sub 2} nanophotocatalyst prepared by novel chemical method

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Xuyao; Zhou, Xiaosong, E-mail: zxs801213@163.com; Zhang, Lingling; Xu, Limei; Ma, Lin; Luo, Jin; Li, Mengjia; Zeng, Lihua

    2015-10-15

    Highlights: • TiO{sub 2} was synthesized through simple one-step hydrothermal method. • Photocatalytic activity for degradation of organic dyes and Cr(VI) are investigated. • The synergistic effect is shown in coexistence of MB and Cr(VI). - Abstract: Fe–N–S-tri-doped TiO{sub 2} (FeNS-TiO{sub 2}) was synthesized by a simple one-step hydrothermal method. The as-synthesized samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopy (XPS). The photocatalytic activities of as-synthesized samples were tested by the oxidation of methyl orange (MO), rhodamine B (RhB), methylene blue (MB) and the reduction of aqueous Cr(VI) under visible-light (λ > 420 nm) irradiation, and compared with N-dope P25 (N-P25) and the undoped TiO{sub 2}. Besides, the effects of the coexistence of MO, RhB, and MB on FeNS-TiO{sub 2}-mediated photocatalytic reduction of aqueous Cr(VI) were also studied. The results indicated FeNS-TiO{sub 2} displayed higher visible-light-activated photocatalytic activity than N-P25 and the undoped TiO{sub 2}. Otherwise, FeNS-TiO{sub 2} showed the coexistence of MB enhanced the photocatalytic reduction of Cr(VI), whereas the coexistence of MO and RhB retarded the photocatalytic reduction of Cr(VI) over FeNS-TiO{sub 2}. Moreover, a possible photocatalytic mechanism is discussed.

  3. A preliminary study on the adsorptive removal of Cr(VI) using seaweed, Hydrilla verticillata

    Energy Technology Data Exchange (ETDEWEB)

    Baral, S.S., E-mail: ss_baral2003@yahoo.co.in [Chemical Engineering Group, Birla Institute of Technology and Science, Pilani - Goa Campus, Zuarinagar, Goa-403726 (India); Das, Namrata; Roy Chaudhury, G.; Das, S.N. [Department of Environment and Sustainability, Institute of Minerals and Materials Technology, Bhubaneswar-751013 (India)

    2009-11-15

    The Cr(VI) adsorption efficiency of the seaweed, Hydrilla verticillata, was studied in batches. The adsorbent was characterized using SEM, BET surface area analyzer, Malvern particle size analyzer, EDAX and FT-IR. Cr(VI) removal efficiency of the adsorbent was studied as a function of different adsorption parameters such as contact time, stirring speed, pH, adsorbent dose, particle size, adsorbate concentration, and temperature. Langmuir, Freundlich, and Temkin adsorption isotherm equations were used in the equilibrium modeling. The adsorption process followed pseudo second-order kinetics and intra-particle diffusion was found to be the rate-controlling step. Experimental data follow Langmuir adsorption isotherm. Thermodynamic parameters such as Gibbs free energy and enthalpy of the adsorption process were evaluated to find out the feasibility of the adsorption process. The negative values of Gibb's free energy and positive enthalpy values show the feasibility and endothermic nature of the process. The significance of different adsorption parameters along with their combined effect on the adsorption process has been established through a full 2{sup 4} factorial design. Among the different adsorption parameters, pH has the most influential effect on the adsorption process followed by adsorbate concentration and combined effects of all the four parameters were tested. The correlation among different adsorption parameters were studied using multi-variate analysis.

  4. The adsorption of Cr(VI) on sulphuric acid-treated wheat bran.

    Science.gov (United States)

    Ozer, A; Ozer, D

    2004-06-01

    Wheat bran, a by-product of wheat milling industries, was converted into a cheap and efficient material by treating with sulphuric acid and used for the adsorption of Cr(VI) from aqueous solution. Effects of various parameters such as initial pH of solution, contact time, initial Cr(VI) concentration and temperature were studied. The sulphuric acid-treated wheat bran (STWB) gave the highest adsorption efficiency at pH 1.5. The equilibrium data were fitted better to Langmuir isotherm model compared to Freundlich model at all the temperatures studied. The adsorption capacity increased from 91 to 133 mg gl(-1) with an increase in temperature from 20 degrees C to 50 degrees C. The adsorption process was found to be endothermic and Langmuir isotherm data were evaluated to determine the thermodynamic parameters for the process. Thermodynamic parameters showed that the process was feasible. The results indicated that the chromium removal process by STWB followed first-order rate expression and adsorption rate constants increased with increasing temperature.

  5. Zeolitic imidazolate framework-8 for efficient adsorption and removal of Cr(VI) ions from aqueous solution.

    Science.gov (United States)

    Niknam Shahrak, Mahdi; Ghahramaninezhad, Mahboube; Eydifarash, Mohsen

    2017-04-01

    Heavy metals are emerging toxic pollutants in which the development of advanced materials for their efficient adsorption and separation is thus of great significance in environmental sciences point of view. In this study, one of the zinc-based zeolitic imidazolate framework materials, known as ZIF-8, has been synthesized and used for chromium(VI) contaminant removal from water for the first time. The as-synthesized ZIF-8 adsorbent was characterized with different methodologies such as powder X-ray diffraction (XRD), thermo-gravimetric analysis, FT-IR, nuclear magnetic resonance spectroscopy, and UV-Vis spectra of solid state. Various factors affecting removal percentage (efficiency) are experimentally investigated including pH of solution, adsorbent dosage, contact time and initial concentration of Cr(VI) to achieve the optimal condition. The obtained results indicate that the ZIF-8 shows good performance for the Cr(VI) removal from aqueous solution so that 60 min mixing of 2 g of ZIF-8 adsorbent with the 2.5 ppm of Cr(VI) solution in a neutral environment will result in the highest separation efficiency around 70%. The time needed to reach the equilibrium (maximum separation efficiency) is only 60 min for a concentration of 5 mg L -1 . Structure stability in the presence of water is also carefully examined by XRD determination of ZIF-8 under different contact times in aqueous solution, which suggests that the structure is going to be destructed after 60 min immersed in solution. Electrostatic interaction of Cr(VI) anions by positively charged ZIF-8 is responsible for Cr(VI) adsorption and separation. Moreover, equilibrium adsorption study reveals that the Cr(VI) removal process using ZIF-8 nicely fits the Langmuir and Toth isotherm models which mean the adsorbent has low heterogeneous surface with different distributions of adsorption energies during Cr(VI) adsorption. Equilibrium adsorption capacity is observed around 0.25 for 20 mg L -1 of initial Cr(VI

  6. Anodic Stripping Voltammetry for the Determination of Trace Cr(VI) with Graphite/Styrene-Acrylonitrile Copolymer Composite Electrodes.

    Science.gov (United States)

    Sari, Trisna K; Jin, Jiye; Zein, Rahmiana; Munaf, Edison

    2017-01-01

    A square-wave anodic stripping voltammetry (SWASV) for the determination of trace amounts of hexavalent chromium Cr(VI) at a graphite/styrene-acrylonitrile (Graphite-SAN) copolymer composite electrode is described. This method involves a preconcentration step whereby the trace Cr(VI) was cathodically reduced to Cr(III) on an electrode surface in an acetate buffer (pH 5), followed by an anodic stripping technique with a square-wave voltammetric mode. It has been shown that the analytical sensitivity is significantly improved at the Graphite-SAN copolymer composite electrode in comparison with the conventional glassy carbon electrode, due to the strong interaction between Cr(III) and the nitrile end group of the SAN copolymer. The SWASV response was characterized with respect to the pH, deposition potential, possible interferences, etc. Under the optimal conditions, the stripping peak height linearly increased with the concentration of Cr(VI) in a range from 0 to 150 ng mL(-1) with a correlation coefficient of 0.997, and a detection limit of 4.2 ng mL(-1) was achieved based on signal-to-noise ratio of about 3. The Graphite-SAN composite electrode exhibited some interesting advantages, such as high mechanical rigid, easy surface renewable, higher sensitivity and better peak resolution in comparison with the results at conventional glassy carbon electrodes. They have been applied to the determination of Cr(VI) in real water samples with satisfactory recoveries.

  7. Preparation and characterization of TiO2/acid leached serpentinite tailings composites and their photocatalytic reduction of chromium(VI).

    Science.gov (United States)

    Sun, Zhiming; Zheng, Liming; Zheng, Shuilin; Frost, Ray L

    2013-08-15

    Composite TiO2/acid leached serpentine tailings (AST) were synthesized through the hydrolysis-deposition method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectrometry (EDS), Fourier-transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and surface area measurement (BET). The XRD analysis showed that TiO2 coated on the surface of acid leached serpentine tailings was mixed crystal phases of rutile and anatase, the grain size of which is 10-30 nm. SEM, TEM, and EDS analysis exhibited that nano-TiO2 particles were deposited on the surface and internal cavities of acid leaching serpentine tailings. The XPS and FT-IR analysis demonstrated that the coating process of TiO2 on AST was a physical adsorption process. The large specific surface area, porous structure, and plentiful surface hydroxyl group of TiO2/AST composite resulted in the high adsorption capacity of Cr(VI). The experimental results demonstrated that initial concentration of Cr(VI), the amount of the catalyst, and pH greatly influenced the removal efficiency of Cr(VI). The removal kinetics of Cr(VI) at a relative low initial concentration was fitted well with Langmuir-Hinshelwood kinetics model with R(2) value of about unity. The as-prepared composites exhibited strong adsorption and photocatalytic capacity for the removal of Cr(VI), and the possible photocatalytic reduction mechanism was studied. The photodecomposition of Cr(VI) was as high as 95% within 2h, and the reusability of the photocatalysis was proven. Copyright © 2013 Elsevier Inc. All rights reserved.

  8. Effect of the gamma irradiation on the bio-sorption of Cr (Vi) by orange peel;Efecto de la irradiacion gamma en la biosorcion de Cr(VI) por cascara de naranja

    Energy Technology Data Exchange (ETDEWEB)

    Lugo L, V.; Barrera D, C. E.; Sanchez M, V. [Universidad Autonoma del Estado de Mexico, Centro de Investigacion en Quimica Sustentable, Paseo Tollocan esquina Paseo Colon s/n, 50180 Toluca, Estado de Mexico (Mexico); Urena N, F., E-mail: violelugol@yahoo.e [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

    2009-07-01

    The orange peel (Citrus sp.) is a bioadsorbent that contains functional groups able to remove Cr (Vi). To study the effect of gamma irradiation in the sorption capacity, the Nn materials were irradiated with gamma rays using a Co{sup 60} source to dose from 10 to 3500 KGy (Nlgamma). The biomass irradiation with gamma rays was successful since it increased the hexavalent chromium removal obtaining a maximum removal percentage of 100%. Sorption isotherms were realized to determine the concentration effect of initial Cr (Vi), the ph effect of the solution and the relationship m/v. (Author)

  9. Cotton fiber/ZrO{sub 2}, a new material for adsorption of Cr(VI) ions in water

    Energy Technology Data Exchange (ETDEWEB)

    Muxel, Alfredo Alberto; Nobre Gimenez, Sonia Maria; Souza Almeida, Flaveli Aparecida de; Silva Alfaya, Reni Ventura da; Silva Alfaya, Antonio Alberto da [Departamento de Quimica, Universidade Estadual de Londrina-UEL, Londrina, PR (Brazil)

    2011-03-15

    The natural cotton fiber was used to synthesize an anion exchange, containing ZrO{sub 2} film on its surface, NCFZC (natural cotton fiber/ZrO{sub 2} composite). This anion exchanger was produced by the reaction of the zirconium oxychloride and hydroxyl groups on surface of the natural cotton fiber. The material was used for Cr(VI) ions adsorption studies. Adsorption equilibrium time and optimum pH for Cr(VI) adsorption were found to be 6 h and 4.0, respectively. The Langmuir and Temkin isotherms were used to models adsorption equilibrium data. The adsorption capacity of NCFZC was found to be 1.33 mmol/g. Kinetic studies showed that the rate of adsorption of Cr(VI) on NCFZC obeyed a pseudo-second-order kinetic model. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  10. Synthesis of a novel illite@carbon nanocomposite adsorbent for removal of Cr(VI) from wastewater.

    Science.gov (United States)

    Wang, Gaofeng; Wang, Shan; Sun, Wen; Sun, Zhiming; Zheng, Shuilin

    2017-07-01

    A novel illite@carbon (I@C) nanocomposite adsorbent has been synthesized via a facile hydrothermal carbonization process (HTC) using glucose as carbonaceous source and illite as the carrier. The morphology, microstructure and surface properties of the prepared nanocomposite adsorbent were analyzed by FESEM, TGA, XRD, FT-IR and Zeta potential measurements. Batch experiments were carried out on the adsorption of Cr(VI) to determine the adsorption properties of the composite. The adsorption of Cr(VI) onto the I@C nanocomposite was well described by the pseudo-second-order kinetic model and Langmuir isotherm. Compared with the illite and carbon material (SC) separately, the prepared I@C nanocomposite adsorbent exhibited enhanced adsorption performance for Cr(VI) with a maximum adsorption capacity of 149.25mg/g, which was higher than that of most reported adsorbents. In addition, the adsorption process was spontaneous and endothermic based on the adsorption thermodynamics study. The adsorption of Cr(VI) by I@C was highly pH-dependent and the optimum adsorption occurred at pH2.0. The Zeta potential analysis results indicated that the electrostatic interactions between anionic Cr(VI) and the positively charged surface of the adsorbent might be critical to the adsorption mechanism. This study demonstrated that the I@C nanocomposite should be a promising candidate for a low-cost, environmental friendly and highly efficient adsorbent for the removal of toxic Cr(VI) from wastewater. Copyright © 2016. Published by Elsevier B.V.

  11. IN VITRO Cr(VI SPECIATION IN SYNTHETIC SALIVA AFTER RELEASING FROM ORTHODONTIC BRACKETS USING SILICA-APTES SEPARATION AND GF AAS DETERMINATION

    Directory of Open Access Journals (Sweden)

    Maciel S. Luz

    Full Text Available A method for Cr(VI speciation in synthetic saliva after releasing from orthodontic brackets, using silica nanoparticles organofunctionalized with (3-aminopropyltriethoxysilane (APTES for Cr(III/Cr(VI separation and GF AAS determination is proposed. Under the optimized conditions, Cr(VI speciation was performed using 150 mg of silica organofunctionalized with 2.0% (v v-1 of APTES at pH 8. It was observed different sensitivity when calibrations of GF AAS were performed using Cr(III or Cr(VI as standard solutions. Consequently, calibrations using stoichiometric mixtures (Cr(III + Cr(VI were used for total Cr determination and calibration using Cr(VI was used only for the determination of this specie. The reliability of the proposed silica-APTES separation procedure and GF AAS determination was checked by addition of both species in synthetic saliva. Recoveries ranging from 97 to 110% were obtained. The repeatability, based on the relative standard deviation (RSD inter days was less than 6%. A corrosion test was carried out on 20 orthodontic brackets from two different models, after immersion in synthetic saliva (pH=6.0 at 37 °C with agitation (125 rpm for 24 h. It was observed that about 40% of the total chromium released from the analyzed orthodontic brackets was Cr(VI.

  12. Luteolin inhibits Cr(VI)-induced malignant cell transformation of human lung epithelial cells by targeting ROS mediated multiple cell signaling pathways

    Energy Technology Data Exchange (ETDEWEB)

    Pratheeshkumar, Poyil; Son, Young-Ok; Divya, Sasidharan Padmaja; Roy, Ram Vinod; Hitron, John Andrew; Wang, Lei [Center for Research on Environmental Disease, University of Kentucky, 1095 VA Drive, Lexington, KY 40536 (United States); Graduate Center for Toxicology, University of Kentucky, 1095 VA Drive, Lexington, KY 40536 (United States); Kim, Donghern; Dai, Jin [Graduate Center for Toxicology, University of Kentucky, 1095 VA Drive, Lexington, KY 40536 (United States); Asha, Padmaja [National Centre for Aquatic Animal Health, Cochin University of Science and Technology, Cochin (India); Zhang, Zhuo [Graduate Center for Toxicology, University of Kentucky, 1095 VA Drive, Lexington, KY 40536 (United States); Wang, Yitao [State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macau (China); Shi, Xianglin, E-mail: xshi5@email.uky.edu [Center for Research on Environmental Disease, University of Kentucky, 1095 VA Drive, Lexington, KY 40536 (United States); Graduate Center for Toxicology, University of Kentucky, 1095 VA Drive, Lexington, KY 40536 (United States)

    2014-12-01

    Hexavalent chromium [Cr(VI)] is a well-known human carcinogen associated with the incidence of lung cancer. Inhibition of metal induced carcinogenesis by a dietary antioxidant is a novel approach. Luteolin, a natural dietary flavonoid found in fruits and vegetables, possesses potent antioxidant and anti-inflammatory activity. We found that short term exposure of human bronchial epithelial cells (BEAS-2B) to Cr(VI) (5 μM) showed a drastic increase in ROS generation, NADPH oxidase (NOX) activation, lipid peroxidation, and glutathione depletion, which were significantly inhibited by the treatment with luteolin in a dose dependent manner. Treatment with luteolin decreased AP-1, HIF-1α, COX-2, and iNOS promoter activity induced by Cr(VI) in BEAS-2B cells. In addition, luteolin protected BEAS-2B cells from malignant transformation induced by chronic Cr(VI) exposure. Moreover, luteolin also inhibited the production of pro-inflammatory cytokines (IL-1β, IL-6, IL-8, TNF-α) and VEGF in chronic Cr(VI) exposed BEAS-2B cells. Western blot analysis showed that luteolin inhibited multiple gene products linked to survival (Akt, Fak, Bcl-2, Bcl-xL), inflammation (MAPK, NF-κB, COX-2, STAT-3, iNOS, TNF-α) and angiogenesis (HIF-1α, VEGF, MMP-9) in chronic Cr(VI) exposed BEAS-2B cells. Nude mice injected with BEAS-2B cells chronically exposed to Cr(VI) in the presence of luteolin showed reduced tumor incidence compared to Cr(VI) alone treated group. Overexpression of catalase (CAT) or SOD2, eliminated Cr(VI)-induced malignant transformation. Overall, our results indicate that luteolin protects BEAS-2B cells from Cr(VI)-induced carcinogenesis by scavenging ROS and modulating multiple cell signaling mechanisms that are linked to ROS. Luteolin, therefore, serves as a potential chemopreventive agent against Cr(VI)-induced carcinogenesis. - Highlights: • Luteolin inhibited Cr(VI)-induced oxidative stress. • Luteolin inhibited chronic Cr(VI)-induced malignant transformation.

  13. Single and combined removal of Cr(VI) and Cd(II) by nanoscale zero-valent iron in the absence and presence of EDDS.

    Science.gov (United States)

    Dong, Haoran; Zeng, Yalan; Xie, Yankai; He, Qi; Zhao, Feng; Wang, Yang; Zeng, Guangming

    2017-09-01

    This study examined the feasibility of nanoscale zero-valent iron (nZVI) for the single and combined removal of Cr(VI) and Cd(II) with or without ethylene diamine disuccinic acid (EDDS). The effects of pH and dissolved oxygen (DO) on the removal process were investigated. Results show that the single removal of either Cr(VI) or Cd(II) by nZVI was pH dependent, where the higher Cr(VI) removal was achieved under acidic conditions, whereas the higher Cd(II) removal was achieved under alkaline conditions. The presence of DO enhanced Cd(II) removal but inhibited Cr(VI) removal under alkaline conditions. In the co-existence of Cr(VI) and Cd(II), it was found that Cd(II) exerted insignificant effect on Cr(VI) removal, while the presence of Cr(VI) remarkably enhanced the Cd(II) removal. The addition of EDDS exhibited different influences on Cr(VI) and Cd(II) removal, which were associated with pH and DO. The EDDS enhanced Cr(VI) removal at pH 5.6-9.0 in the absence of DO, but decreased Cr(VI) removal at pH 9.0 in the presence of DO. For the removal of Cd(II) at pH 5.6-7.0, either facilitation or inhibition effect of EDDS was observed, depending on EDDS concentration and the co-existence of Cr(VI). However, Cd(II) removal was always significantly inhibited by EDDS at pH 9.0.

  14. Lead chromate detected as a source of atmospheric Pb and Cr (VI) pollution

    Science.gov (United States)

    Lee, Pyeong-Koo; Yu, Soonyoung; Chang, Hye Jung; Cho, Hye Young; Kang, Min-Ju; Chae, Byung-Gon

    2016-10-01

    Spherical black carbon aggregates were frequently observed in dust dry deposition in Daejeon, Korea. They were tens of micrometers in diameter and presented a mixture of black carbon and several mineral phases. Transmission electron microscopy (TEM) observations with energy-dispersive X-ray spectroscopy (EDS) and selected area diffraction pattern (SADP) analyses confirmed that the aggregates were compact and included significant amounts of lead chromate (PbCrO4). The compositions and morphologies of the nanosized lead chromate particles suggest that they probably originated from traffic paint used in roads and were combined as discrete minerals with black carbon. Based on Pb isotope analysis and air-mass backward trajectories, the dust in Daejeon received a considerable input of anthropogenic pollutants from heavily industrialized Chinese cities, which implies that long-range transported aerosols containing PbCrO4 were a possible source of the lead and hexavalent chromium levels in East Asia. Lead chromate should be considered to be a source of global atmospheric Pb and Cr(VI) pollution, especially given its toxicity.

  15. Lead chromate detected as a source of atmospheric Pb and Cr (VI) pollution.

    Science.gov (United States)

    Lee, Pyeong-Koo; Yu, Soonyoung; Chang, Hye Jung; Cho, Hye Young; Kang, Min-Ju; Chae, Byung-Gon

    2016-10-25

    Spherical black carbon aggregates were frequently observed in dust dry deposition in Daejeon, Korea. They were tens of micrometers in diameter and presented a mixture of black carbon and several mineral phases. Transmission electron microscopy (TEM) observations with energy-dispersive X-ray spectroscopy (EDS) and selected area diffraction pattern (SADP) analyses confirmed that the aggregates were compact and included significant amounts of lead chromate (PbCrO4). The compositions and morphologies of the nanosized lead chromate particles suggest that they probably originated from traffic paint used in roads and were combined as discrete minerals with black carbon. Based on Pb isotope analysis and air-mass backward trajectories, the dust in Daejeon received a considerable input of anthropogenic pollutants from heavily industrialized Chinese cities, which implies that long-range transported aerosols containing PbCrO4 were a possible source of the lead and hexavalent chromium levels in East Asia. Lead chromate should be considered to be a source of global atmospheric Pb and Cr(VI) pollution, especially given its toxicity.

  16. Removal of Cr(VI ions from waste water by electrocoagulation using iron electrode

    Directory of Open Access Journals (Sweden)

    Yehia A. El-Taweel

    2015-06-01

    Full Text Available The performance of electrocoagulation using iron electrodes for the treatment of aqueous solutions containing chromium hexavalent ions using fixed bed electrochemical batch reactor was studied. A new anode design consisting of hex nuts was connected together with a thin rode of iron. The helical shape in the nuts increases the anode surface area allowing high chromium removal rate within very short coagulation time. The effect of different parameters affecting the electrocoagulation process, such as initial hexavalent chromium concentration, applied current, electrolyte type [sodium chloride and sodium sulfate] concentration and initial pH of the solution was investigated. The optimum conditions for the EC process by using the present cell based on minimum initial hexavalent chromium concentration, energy consumption and operating cost were 100 mg of Cr(VI/l, 0.55 A, 1.5 g of sodium chloride/land pH of 1.

  17. Development of iron-based nanoparticles for Cr(VI removal from drinking water

    Directory of Open Access Journals (Sweden)

    Vourlias G.

    2013-01-01

    Full Text Available A great deal of research over recent decades has been motivated by the requirement to lower the concentration of chromium in drinking water. This study has been conducted to determine the feasibility of iron-based nanoparticles for chromium removal from contaminated water. Single Fe, Fe3O4 and binary Fe/Fe3O4 nanoparticles were grown at the 45-80 nm size range using the solar physical vapor deposition technique and tested as potential hexavalent chromium removing agents from aqueous solutions. Due to their higher electron donation ability compared to the Fe3O4 ones, single Fe nanoparticles exhibited the highest Cr(VI removal capacity of more than 3 µg/mg while maintaining a residual concentration 50 µg/L, equal to the regulation limit for drinking water. In combination to their facile and fast magnetic separation, the applicability of the studied particles in water treatment facilities should be considered.

  18. The Adsorption of Cr(VI Using Chitosan-Alumina Adsorbent

    Directory of Open Access Journals (Sweden)

    Darjito Darjito

    2013-12-01

    Full Text Available Chitosan as adsorbent has been used widely, however it was not effective yet for metal ions adsorption in industrial scale. In acidic condition, chitosan’s active site tends to decrease. This drawback can was solved by coating of chitosan active site on alumina. This paper discloses to overcome that limitation. The charateristic of the active side was analysed by FTIR spectrometry toward vibration N-H group at 1679.15 cm-1, C=O group of oxalate at 1703.30 cm-1, and Al-O group of alumina at 924.07 cm-1. The adsorption capacity of the developed adsorbent was tester to adsorb Cr(VI ions under various of pH value such as 1, 2, 3, 4, 5, 6, and 7. The contact time affect toward the adsorption was also reported in 20, 30, 40 50, 60, 70, and 80 minute. In addition, the concentration effects (100, 200, 300, 400, 500, and 600 ppm was also studied. Chromium (VI was measured using spectronic-20. Adsorption capacity was obtained at 66.90 mg/g under optimum conditions pH 2, and contact time 60 minute, respectively.

  19. Simultaneous Adsorption of Cr(VI and Phenol from Binary Mixture Using Iron Incorporated Rice Husk: Insight to Multicomponent Equilibrium Isotherm

    Directory of Open Access Journals (Sweden)

    Ankur Gupta

    2016-01-01

    Full Text Available Fe modified rice husk was prepared as a low cost biosorbent for the removal of Cr(VI and phenol both singly and in combination from single and binary simulated synthetic waste water. Rice husk was modified by treating with FeSO4·7H2O. The results showed that impregnation of iron onto the surface of rice husk improved the adsorption capability of both Cr(VI and phenol. The effects of process parameters for multicomponent system such as pH, adsorbent dose, and contact time onto the percentage removal of both Cr(VI and phenol were investigated. The experimental data for the adsorption of both Cr(VI and phenol onto the surface of Fe modified rice husk applied to various kinetic and adsorption isotherm models. Multicomponent isotherm models such as Nonmodified Langmuir, Modified Langmuir, Extended Langmuir, Extended Freundlich, Competitive Nonmodified Redlich Peterson, Competitive Modified Redlich Peterson were applied. The results show that Extended Freundlich model best described the experimental data for both Cr(VI and phenol from binary solution. Pseudo second-order model agreed well with Cr(VI while pseudo first-order model agreed well with phenol. Maximum adsorption capacity in synthetic binary solution of Cr(VI and phenol was found to be 36.3817 mg g−1 for Cr(VI and 6.569 mg g−1 for phenol, respectively.

  20. Karakterisasi Adsorben dari Kulit Manggis dan Kinerjanya pada Adsorpsi Logam Pb(II dan Cr(VI - (Adsorbent Characterization from Mangosteen Peel and Its Adsorption Performance on Pb(II and Cr(VI

    Directory of Open Access Journals (Sweden)

    Ulfa Haura

    2017-06-01

    Full Text Available The usage of biomass waste-based adsorbent for the adsorption of hazardous metal in wastewater is not only reducing waste but also lowering adsorbent price. This research aims to study the characteristics of adsorbent from mangosteen peel (Garcinia Mangostana L. and activated charcoal from mangosteen peel, also to compare the adsorption performance on metal ion Pb(II and Cr(VI. Synthetic wastewater used from a solution of Pb(NO32 and K2Cr2O7 with variations in initial concentration of 20, 40, 80, 100 and 200 mg/L. Adsorption performed at pH 5, ratio of adsorbent and waste solution 1/200 (w/v, 60 rpm, 0.5 gs nano-sized adsorbent. Characterization using SEM, FTIR and SEM-EDS showed that both adsorbents characteristics met the requirements of SNI 06-3730-1995. The highest adsorption capacity of activated carbon to adsorb Pb(II and Cr(VI were 38.543 mg/g and 36.838 mg/g while biosorbent adsorb Pb(II and Cr(VI respectively 3.98 mg/g and 36.12 mg/g.Keywords: adsorption, biosorbent, Cr(VI, mangosteen peel, Pb(IIABSTRAKPenggunaan adsorben berbasis limbah biomassa untuk adsorpsi kandungan logam berbahaya dari limbah cair industri selain dapat mengurangi limbah juga dapat menekan harga jual adsorben. Penelitian ini bertujuan untuk mempelajari karakteristik adsorben yang terbuat dari limbah kulit manggis (Garcinia mangostana L. dan arang aktif dari limbah kulit manggis serta membandingkan kinerja kedua jenis adsorben tersebut pada proses adsorpsi ion logam Pb(II dan Cr(VI. Limbah sintetis yang digunakan berupa ion dari Pb(II dan Cr(VI dari larutan Pb(NO32 dan K2Cr2O7 dengan variasi konsentrasi awal 20, 40, 80, 100 dan 200 mg/L. Proses adsorpsi dilakukan pada pH 5, rasio perbandingan berat adsorben dan volume larutan limbah 1:200, kecepatan pengadukan 60 rpm, adsorben berukuran nano dengan berat adsorben 0,5 g. Masing-masing adsorben dikarakterisasi menggunakan SEM untuk mengetahui sturktur morfologi, FTIR untuk mengetahui gugus fungsi dan SEM-EDS untuk

  1. Impact of Cr(VI) on P removal performance in enhanced biological phosphorus removal (EBPR) system based on the anaerobic and aerobic metabolism.

    Science.gov (United States)

    Fang, Jing; Sun, Pei-de; Xu, Shao-juan; Luo, Tao; Lou, Ju-qing; Han, Jing-yi; Song, Ying-qi

    2012-10-01

    Influence of Cr(VI) on P removal in enhanced biological phosphorus removal (EBPR) system was investigated with respect to the composition of poly-phosphate-accumulating organisms (PAOs) and glycogen accumulating organisms (GAOs), the transformation of poly-β-hydroxyalkanoates (PHA) and glycogen, enzymes' activities, and the intracellular Cr. Whether EBPR system could revive after Cr(VI) shock was also explored. Results showed P removal performance was completely inhibited by Cr(VI) with the concentration more than 5 mg L(-1). PAOs were more sensitive to Cr(VI) than GAOs and the other bacteria were. PHA consumption, glycogen synthesis and adenylate kinase's activity had been inhibited by 5 mg L(-1) Cr(VI). Both adenylate kinase's activity and P removal efficiency were negatively correlated with the intracellular Cr. Recovery experiments revealed that P removal performance with 5 mg L(-1) Cr(VI) shock could revive after a 2-day recovery treatment, while systems with high level Cr(VI) (20 and 60 mg L(-1)) shock could not. Copyright © 2012 Elsevier Ltd. All rights reserved.

  2. Biosorption of Cr(VI) from aqueous solution by chemically modified potato starch: equilibrium and kinetic studies.

    Science.gov (United States)

    Pillai, Saumya S; Mullassery, Manohar D; Fernandez, Noeline B; Girija, N; Geetha, P; Koshy, Mathew

    2013-06-01

    The biosorption capacity of chemically modified potato starch (CPS) for Cr(VI) from aqueous solution was investigated. The materials derived from carbohydrates are biodegradable and are generally regarded as safe and environmentally acceptable. The hydroxyl, carboxyl and carbonyl groups are responsible for the biosorption process. In the present study, the influence of various important parameters such as pH, time, biosorbent dose and initial Cr(VI) concentration on the biosorption capacity were investigated. The isotherms such as Langmuir, Freundlich and Tempkin were studied. The Freundlich and the Redlich-Peterson isotherms had been well fitted the biosorption of Cr(VI) with chemically modified potato starch. The kinetics of Cr(VI) removal using chemically modified potato starch was well explained by second-order kinetic model. The thermodynamic parameters were also evaluated from the biosorption measurements. Among the various desorbing agents tested, 98.2 percent chromium recovery was achieved with 0.1molL(-1) NaOH. Copyright © 2013 Elsevier Inc. All rights reserved.

  3. Removal of Cr(VI) from aqueous solutions by low-cost biosorbents: Marine macroalgae and agricultural by-products

    Energy Technology Data Exchange (ETDEWEB)

    Wang Xuesong [Department of Chemical Engineering, Huaihai Institute of Technology, Lianyungang, Jiangsu 222005 (China)], E-mail: snowpine1969@yahoo.com.cn; Li Zhizhong [Department of Chemical Engineering, Huaihai Institute of Technology, Lianyungang, Jiangsu 222005 (China); Sun Cheng [School of the Environment, Nanjing University, Nanjing, Jiangsu 210093 (China)

    2008-05-30

    In this study, adsorption of Cr(VI) onto the four low-cost biosorbents (Laminaria japonica, P. yezoensis Ueda, rice bran and wheat bran) was investigated depending on solution pH, contact time, adsorbent concentration and adsorption isotherms by employing batch adsorption technique. The adsorption capacities were significantly influenced by solution pH, with lower pH favoring higher Cr(VI) removal for various biosorbents. The ionic strength of NaCl was also observed to have a significant impact on the Cr(VI) adsorption due to the competition of Cl{sup -} in the aqueous solutions. The batch equilibrium data were correlated to Langmuir and Freundlich isotherms and the data fitted better to the Freundlich isotherm equation. The apparent thermodynamic parameters were calculated for each of the four biosorbents and the obtained numerical values showed that the Cr(VI) adsorption onto the various low-cost biosorbents is spontaneous, entropy-driven and endothermic processes. The batch kinetic data were correlated to the pseudo-first order and pseudo-second order models and the data fitted better to the pseudo-second order equation. An intraparticle diffusion model was applied to investigate the adsorption mechanisms. The adsorption capacities for various biosorbents studied in this work were inversely proportional to the adsorbent concentrations.

  4. Selective removal of Cr(VI) from aqueous solution by polypyrrole/2,5-diaminobenzene sulfonic acid composite

    CSIR Research Space (South Africa)

    Kera, Nazia H

    2016-08-01

    Full Text Available A polypyrrole/2,5-diaminobenzenesulfonic acid (PPy/DABSA) composite, synthesised by the in situ oxidative polymerization of pyrrole in the presence of DABSA, was studied as an adsorbent for the removal of Cr(VI) from aqueous solution. The structure...

  5. Biosorption of Cr(VI), Ni(II) and Fe(II) by maize ( zea mays ) cob ...

    African Journals Online (AJOL)

    The experimental results for the biosorption of Cr(VI), Ni(II) and Fe(II) onto maize cob were reported. The adsorbents efficiency on the bioremediation of these metals was estimated from the change in the percent adsorbate removal with (i) adsorbent dosage (ii) adsorbate initial concentration, (iii) variation in pH of the ...

  6. Plant-mediated synthesis of highly active iron nanoparticles for Cr (VI) removal: Investigation of the leading biomolecules.

    Science.gov (United States)

    Xiao, Zhengli; Yuan, Min; Yang, Bin; Liu, Zhaoyan; Huang, Jiale; Sun, Daohua

    2016-05-01

    The eco-friendly synthesis and application of Fe nanoparticles (Fe NPs) with higher activity and stability has aroused wide attention in the field of pollutant remediation. In this work, 15 plants extracts were selected for the plant-mediated synthesis of Fe NPs. The as-synthesized particles' morphology and structure were characterized by transmission electron microscopy, X-ray diffraction and UV-Vis spectroscopy. The contents of four main active biomolecules in the 15 extracts were determined, and comparative studies were further carried out to clarify the key component closely related to the reducing capacity. The results demonstrate that polyphenol is the leading ingredient involved in the biosynthesis of Fe NPs. Then Fe products synthesized by three extracts with distinct content of polyphenol were employed to remove Cr (VI) in the aqueous solution, indicating that the activity of the Fe NPs for Cr (VI) removal is consistent with the reducing capacity of the extracts. Furthermore, the Fe NPs synthesized by S. jambos(L.) Alston extract (SJA-Fe NPs) showed significant removal capacity of Cr(VI) with 698.6 mg Cr(VI) per g of iron. Copyright © 2016 Elsevier Ltd. All rights reserved.

  7. Highly effective removal of toxic Cr(VI) from wastewater using sulfuric acid-modified avocado seed

    CSIR Research Space (South Africa)

    Bhaumik, M

    2014-01-01

    Full Text Available Sulfuric acid modified avocado seed (ASSA), as a low-cost carbonized adsorbent, was investigated for the removal of toxic Cr(VI) from water/wastewater in batch experiments. A low temperature (100 °C) chemical carbonization treatment was employed...

  8. Competitive Adsorption of Cd(II), Cr(VI), and Pb(II) onto Nanomaghemite: A Spectroscopic and Modeling Approach.

    Science.gov (United States)

    Komárek, Michael; Koretsky, Carla M; Stephen, Krishna J; Alessi, Daniel S; Chrastný, Vladislav

    2015-11-03

    A combined modeling and spectroscopic approach is used to describe Cd(II), Cr(VI), and Pb(II) adsorption onto nanomaghemite and nanomaghemite coated quartz. A pseudo-second order kinetic model fitted the adsorption data well. The sorption capacity of nanomaghemite was evaluated using a Langmuir isotherm model, and a diffuse double layer surface complexation model (DLM) was developed to describe metal adsorption. Adsorption mechanisms were assessed using X-ray photoelectron spectroscopy and X-ray absorption spectroscopy. Pb(II) adsorption occurs mainly via formation of inner-sphere complexes, whereas Cr(VI) likely adsorbs mainly as outer-sphere complexes and Cd(II) as a mixture of inner- and outer-sphere complexes. The simple DLM describes well the pH-dependence of single adsorption edges. However, it fails to adequately capture metal adsorption behavior over broad ranges of ionic strength or metal-loading on the sorbents. For systems with equimolar concentrations of Pb(II), Cd(II), and Cr(VI). Pb(II) adsorption was reasonably well predicted by the DLM, but predictions were poorer for Cr(VI) and Cd(II). This study demonstrates that a simple DLM can describe well the adsorption of the studied metals in mixed sorbate-sorbent systems, but only under narrow ranges of ionic strength or metal loading. The results also highlight the sorption potential of nanomaghemite for metals in complex systems.

  9. Degradation of phenol and Cr (VI) wastewater with contact glow discharge electrolysis method and the addition of Fe2+

    Science.gov (United States)

    Kurniawan, Raden Ridzki Aditya; Saksono, Nelson

    2017-11-01

    Phenol and Cr (VI) are an organic waste and dangerous heavy metals which generated from a wide variety of industrial processes such as textiles, paints, dyes, and others. For that reason, we need effective waste treatment technologies, one of them is Contact Glow Discharge Electrolysis (CGDE). This method produce reactive species such as radical hidroxyl so as to be able to degradate phenol and Cr(VI) wastewater effectively. This research aims to obtain the effect of Fe 2+ and air bubbles in degradation of phenol and Cr (VI) waste simultaneously. Waste degradation is measured its absorbance with UV-Vis spectrophotometer. In the conditions of 600 Volt voltage, Na2SO4 0.02 M, anode depth of 1.5 cm, the addition of Fe2+ 40 ppm and the addition of air bubbles for 30 minutes was obtained a percentage degradation of phenol 99.47%, Cr (VI) 76.75% and specific energy of 344.473 kJ / mmol.

  10. Flow injection on-line preconcentration of low levels of Cr(VI) with detection by ETAAS

    DEFF Research Database (Denmark)

    Som-aum, Waraporn; Liawruangrath, Saisunee; Hansen, Elo Harald

    2002-01-01

    A flow injection (FI) on-line sorption preconcentration procedure utilizing a packed column reactor and combined with electrothermal atomic absorption spectrometry (ETAAS) is proposed for the determination of low levels of Cr(VI) in water samples. Polytetrafluoroethylene (PTFE) beads packed...

  11. Grafting of β-cyclodextrin to magnetic graphene oxide via ethylenediamine and application for Cr(VI) removal.

    Science.gov (United States)

    Wang, Hui; Liu, Yun-guo; Zeng, Guang-ming; Hu, Xin-jiang; Hu, Xi; Li, Ting-ting; Li, Hua-ying; Wang, Ya-qin; Jiang, Lu-hua

    2014-11-26

    A novel β-cyclodextrin (β-CD) polymer adsorbent named β-cyclodextrin/ethylenediamine/magnetic graphene oxide (CD-E-MGO) was synthesized for decontamination of Cr(VI) from aqueous solution. The sorption kinetics, isotherms and thermodynamics, as well as the effects of pH, aniline and ionic strength on the sorption process were investigated. The results indicated that CD-E-MGO could effectively remove Cr(VI) from aqueous solution and the sorption data could be well described by pseudo-second-order and Langmuir models. The intraparticle diffusion study indicated that intraparticle diffusion was not the only rate-limiting step. Thermodynamic parameters revealed that the sorption reaction was an endothermic and spontaneous process. The decontamination of Cr(VI) was influenced by solution pH and ionic strength. In the system with aniline, the Cr(VI) sorption was improved at low pH values but reduced at high pH values. These results are important for estimating and optimizing the removal of metal ions by CD-E-MGO composite. Copyright © 2014 Elsevier Ltd. All rights reserved.

  12. High performance NiFe layered double hydroxide for methyl orange dye and Cr(VI) adsorption.

    Science.gov (United States)

    Lu, Yi; Jiang, Bin; Fang, Liang; Ling, Faling; Gao, Jiemei; Wu, Fang; Zhang, Xihua

    2016-06-01

    The NiFe layered double hydroxides (LDHs) with different mole ratio of Ni/Fe (4:1, 3:1, 7:3 and 1:1) were prepared by a simple coprecipitation method. The adsorption performance were evaluated by the removal of methyl orange (MO) dye and hexavalent chromium(VI) heavy metal ion. It is found that Ni4Fe1-LDH can remove more than 92% of MO in 10 min at the 10 mg/L MO initial concentration, and 97% of Cr(VI) in 1 h at 4 mg/L Cr2O7(2-) initial concentration. The saturated adsorption capacity of Ni4Fe1-LDH is found to be as large as 205.76 mg/g for MO and 26.78 mg/g for Cr(VI). The adsorption behavior of this new adsorbent is fitted well with Langmuir isotherm and the pseudo-second-order kinetic model, indicative of a monolayer and chemical adsorption that synergistically originates from exchangeable anions mechanism and layer charge density. Due to the excellent removal capacity of MO and Cr(VI), the NiFe-LDHs could be a promising adsorbent for wastewater treatment. Copyright © 2016 Elsevier Ltd. All rights reserved.

  13. Microwave assisted preparation of n-butylacrylate grafted chitosan and its application for Cr(VI) adsorption.

    Science.gov (United States)

    Santhana Krishna Kumar, A; Uday Kumar, Chinta; Rajesh, Vidya; Rajesh, N

    2014-05-01

    Biopolymers such as chitosan possess excellent properties suited for varied applications. In this work, we describe a novel microwave assisted method for the preparation of n-butylacrylate grafted chitosan adsorbent and its utility for the adsorption of chromium(VI). A 3 min irradiation time was enough to prepare the adsorbent, and techniques such as FT-IR, powder XRD, SEM and EDS were used for comprehensive characterization. The adsorption was effective at pH 3.5 with 25 mL of 20 ppm Cr(VI) solution. Langmuir, Freundlich, Dubinin-Radushkevich, Temkin, Elovich and Redlich isotherms were studied in detail. The ΔG, ΔH and ΔS parameters were evaluated to understand the adsorption thermodynamics. The adsorption involves the interaction of Cr(VI) with the hydroxyl and amino groups in chitosan. Copyright © 2014 Elsevier B.V. All rights reserved.

  14. Hydrothermal derived nitrogen doped SrTiO3 for efficient visible light driven photocatalytic reduction of chromium(VI).

    Science.gov (United States)

    Xing, Guanjie; Zhao, Lanxiao; Sun, Tao; Su, Yiguo; Wang, Xiaojing

    2016-01-01

    In this work, we report on the synthesis of nitrogen doped SrTiO3 nanoparticles with efficient visible light driven photocatalytic activity toward Cr(VI) by the solvothermal method. The samples are carefully characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, UV-Vis diffuse reflectance spectroscopy and photocatalytic test. It is found that nitrogen doping in SrTiO3 lattice led to an apparent lattice expansion, particle size reduction as well as subsequent increase of Brunner-Emmet-Teller surface area. The visible light absorption edge and intensity can be modulated by nitrogen doping content, which absorption edge extends to about 600 nm. Moreover, nitrogen doping can not only modulate the visible light absorption feature, but also have consequence on the enhancement of charge separation efficiency, which can promote the photocatalytic activity. With well controlled particle size, Brunner-Emmet-Teller surface area, and electronic structure via nitrogen doping, the photocatalytic performance toward Cr(VI) reduction of nitrogen doped SrTiO3 was optimized at initial hexamethylenetetramine content of 2.

  15. Catalytic activity of Ni complexed aminoclay towards the reduction of Cr(V), p-nitrophenol and fluorescein dye

    Science.gov (United States)

    Ranchani, A. Amala Jeya; Parthasarathy, V.; Devi, A. Anitha; Meenarathi, B.; Anbarasan, R.

    2017-09-01

    A green-colored Ni-complexed aminoclay (AC) was synthesized and its size and crystalline nature were confirmed by HRTEM images and XRD, respectively. The AC-Ni system was used as a catalyst towards the reduction of environmental pollutants like Cr(VI), fluorescein (Fluor) and nitrophenol (NiP) individually and also their mixture. The catalytic reduction of Cr(VI) was elaborately studied under different experimental conditions. The thermodynamic parameters were determined. The AC-Ni system exhibited lower energy of activation (E a) value. The apparent rate constant of individual components and their mixture was determined, analyzed and compared with the literature reports. The pollutants present in the mixture exhibited the lower k app value due to the complex formation.

  16. Catalytic activity of Ni complexed aminoclay towards the reduction of Cr(V), p-nitrophenol and fluorescein dye

    Science.gov (United States)

    Ranchani, A. Amala Jeya; Parthasarathy, V.; Devi, A. Anitha; Meenarathi, B.; Anbarasan, R.

    2017-11-01

    A green-colored Ni-complexed aminoclay (AC) was synthesized and its size and crystalline nature were confirmed by HRTEM images and XRD, respectively. The AC-Ni system was used as a catalyst towards the reduction of environmental pollutants like Cr(VI), fluorescein (Fluor) and nitrophenol (NiP) individually and also their mixture. The catalytic reduction of Cr(VI) was elaborately studied under different experimental conditions. The thermodynamic parameters were determined. The AC-Ni system exhibited lower energy of activation ( E a) value. The apparent rate constant of individual components and their mixture was determined, analyzed and compared with the literature reports. The pollutants present in the mixture exhibited the lower k app value due to the complex formation.

  17. Rates of Cr(VI) Generation from CrxFe1-x(OH)3Solids upon Reaction with Manganese Oxide.

    Science.gov (United States)

    Pan, Chao; Liu, Huan; Catalano, Jeffrey G; Qian, Ao; Wang, Zimeng; Giammar, Daniel E

    2017-11-07

    The reaction of manganese oxides with Cr(III)-bearing solids in soils and sediments can lead to the natural production of Cr(VI) in groundwater. Building on previous knowledge of MnO 2 as an oxidant for Cr(III)-containing solids, this study systematically evaluated the rates and mechanisms of the oxidation of Cr(III) in iron oxides by δ-MnO 2 . The Fe/Cr ratio (x = 0.055-0.23 in Cr x Fe 1-x (OH) 3 ) and pH (5-9) greatly influenced the Cr(VI) production rates by controlling the solubility of Cr(III) in iron oxides. We established a quantitative relationship between Cr(VI) production rates and Cr(III) solubility of Cr x Fe 1-x (OH) 3 , which can help predict Cr(VI) production rates at different conditions. The adsorption of Cr(VI) and Mn(II) on solids shows a typical pH dependence for anions and cations. A multichamber reactor was used to assess the role of solid-solid contact in Cr x Fe 1-x (OH) 3 -MnO 2 interactions, which eliminates the contact of the two solids while still allowing aqueous species transport across a permeable membrane. Cr(VI) production rates were much lower in multichamber than in completely mixed batch experiments, indicating that the redox interaction is accelerated by mixing of the solids. Our results suggest that soluble Cr(III) released from Cr x Fe 1-x (OH) 3 solids to aqueous solution can migrate to MnO 2 surfaces where it is oxidized.

  18. Disruption of putrescine biosynthesis in Shewanella oneidensis enhances biofilm cohesiveness and performance in Cr(VI) immobilization.

    Science.gov (United States)

    Ding, Yuanzhao; Peng, Ni; Du, Yonghua; Ji, Lianghui; Cao, Bin

    2014-02-01

    Although biofilm-based bioprocesses have been increasingly used in various applications, the long-term robust and efficient biofilm performance remains one of the main bottlenecks. In this study, we demonstrated that biofilm cohesiveness and performance of Shewanella oneidensis can be enhanced through disrupting putrescine biosynthesis. Through random transposon mutagenesis library screening, one hyperadherent mutant strain, CP2-1-S1, exhibiting an enhanced capability in biofilm formation, was obtained. Comparative analysis of the performance of biofilms formed by S. oneidensis MR-1 wild type (WT) and CP2-1-S1 in removing dichromate (Cr2O7(2-)), i.e., Cr(VI), from the aqueous phase showed that, compared with the WT biofilms, CP2-1-S1 biofilms displayed a substantially lower rate of cell detachment upon exposure to Cr(VI), suggesting a higher cohesiveness of the mutant biofilms. In addition, the amount of Cr(III) immobilized by CP2-1-S1 biofilms was much larger, indicating an enhanced performance in Cr(VI) bioremediation. We further showed that speF, a putrescine biosynthesis gene, was disrupted in CP2-1-S1 and that the biofilm phenotypes could be restored by both genetic and chemical complementations. Our results also demonstrated an important role of putrescine in mediating matrix disassembly in S. oneidensis biofilms.

  19. Reduction and Simultaneous Removal of 99 Tc and Cr by Fe(OH) 2 (s) Mineral Transformation

    Energy Technology Data Exchange (ETDEWEB)

    Saslow, Sarah A. [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99354, United States; Um, Wooyong [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99354, United States; Pearce, Carolyn I. [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99354, United States; Engelhard, Mark H. [Environmental; Bowden, Mark E. [Environmental; Lukens, Wayne [Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, California 94720, United States; Leavy, Ian I. [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99354, United States; Riley, Brian J. [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99354, United States; Kim, Dong-Sang [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99354, United States; Schweiger, Michael J. [Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99354, United States; Kruger, Albert A. [United

    2017-07-17

    Technetium (Tc) remains a priority remediation concern due to persistent challenges, including rapid re-oxidation of immobilized Tc, and competing contaminants, e.g. Cr(VI), that inhibit targeted Tc reduction and incorporation into stable mineral phases. Here Fe(OH)2(s) is investigated as a comprehensive solution for overcoming these challenges, by serving as both the reductant, (Fe(II)), and immobilization agent to form Tc-incorporated magnetite (Fe3O4). Trace metal analysis suggests removal of Tc(VII) and Cr(VI) from solution occurs simultaneously; however, complete removal and reduction of Cr(VI) is achieved earlier than the removal/reduction of co-mingled Tc(VII). Bulk oxidation state analysis of the magnetite solid phase by XANES confirms that the majority of Tc is Tc(IV), which is corroborated by XPS. Furthermore, EXAFS results show successful Tc(IV) incorporation into magnetite octahedral sites without additional substitution of Cr or Tc into neighboring Fe octahedral sites. XPS analysis of Cr confirms reduction to Cr(III) and the formation of a Cr-incorporated spinel, Cr2O3, and Cr(OH)3 phases. Spinel (modeled as Fe3O4), goethite, and feroxyhyte are detected in all reacted solid phase samples analyzed by XRD, where Tc(IV) incorporation has little effect on the spinel lattice structure. In the presence of Cr(III) a spinel phase along the magnetite-chromite (Fe3O4-FeCr2O4) solid-solution line is formed.

  20. A facile, versatile approach to hydroxyl-anchored metal oxides with high Cr(VI) adsorption performance in water treatment

    Science.gov (United States)

    Ma, Ji; Zuo-Jiang, SiZhi; He, Yunhao; Sun, Qinglei; Wang, Yunguo; Liu, Wei; Sun, Shuangshuang; Chen, Kezheng

    2016-11-01

    In this study, a facile and versatile urea-assisted approach was proposed to synthesize Chinese rose-like NiO, pinecone-like ZnO and sponge-like CoO adsorbents. The presence of urea during syntheses endowed these adsorbents with high concentration of surface hydroxyl groups, which was estimated as 1.83, 1.32 and 4.19 mmol [OH-] g-1 for NiO, ZnO and CoO adsorbents, respectively. These surface hydroxyl groups would facilitate the adsorption of Cr(vi) species (e.g. HCrO4-, Cr2O72- and CrO42-) from wastewater by exchanging with hydroxyl protons or hydroxide ions, and hence result in extremely high maximum adsorbed amounts of Cr(vi), being 2974, 14 256 and 408 mg g-1 for NiO, ZnO and CoO adsorbents in the pH range of 5.02-5.66 at 298 K, respectively. More strikingly, the maximum adsorbed amounts of Cr(vi) would be greatly enhanced as the adsorbing temperature is increased, and even amount to 23 411 mg g-1 for ZnO adsorbents at 323 K. Based on the kinetics and equilibrium studies of adsorptive removal of Cr(vi) from wastewater, our synthetic route will greatly improve the adsorptivity of the as-synthesized metal-oxide adsorbents, and hence it will shed new light on the development of high-performance adsorbents.

  1. A new turn-on fluorimetric method for the rapid speciation of Cr(III)/Cr(VI) species in tea samples with rhodamine-based fluorescent reagent

    Science.gov (United States)

    Özyol, Esra; Saçmacı, Şerife; Saçmacı, Mustafa; Ülgen, Ahmet

    2018-02-01

    A new fluorimetric method with rhodamine-based fluorescent agent was developed for the rapid speciation of Cr(III)/Cr(VI) in tea, soil and water samples. The system, which utilizes a fluorescent reagent, was used for the first time after synthesis/characterization of 3‧,6‧-bis(diethylamino)-2-{[(1E)-(2,4-dimethoxyphenyl)methylene] amino}spiro[isoindole-1,9‧-xanthen]-3(2H)-one (BDAS). The reagent responds instantaneously at room temperature in a 1:1 stoichiometric manner to the amount of Cr(III). The selectivity of this system for Cr(III) over other metal ions is remarkably high, and its sensitivity is below 0.01 mg L- 1 in aqueous solutions which enables a simplification without any pretreatment of the real sample. The method has a wide linear range of 0.1-10 mg L- 1 and a detection limit of 0.15 μg L- 1 for Cr(III) while the relative standard deviation was 0.1% for 0.1 mg L- 1 Cr(III) concentration. The results of detection and recovery experiments for Cr(III) in tea, soil and water were satisfactory, indicating that the method has better feasibility and application potential in the routine determination and speciation of Cr(III)/Cr(VI). The results of analysis of the certified reference material (INCT-TL-1 tea sample and CWW-TM-D waste water) are in good agreement with the certified value.

  2. Integrated Investigation on the Production and Fate of Organo-Cr(III) Complexes from Microbial Reduction of Chromate

    Energy Technology Data Exchange (ETDEWEB)

    Xun, Luying

    2005-06-01

    Our objective is to investigate the complexity of chromium biogeocycling. Our results clearly support more complexity. In short, the chromium cycle is not as simple as the conversion between Cr(III) and Cr(VI) in inorganic forms. We have obtained more evidence to prove the formation of soluble organo-Cr(III) complexes from microbial reduction of Cr(VI). The complexes are relatively stable due to the slow ligand exchange of Cr(III). However, some microorganisms can consume the organic ligands and release Cr(III), which then precipitates. Efforts are being made to characterize the organo-Cr(III) complexes and investigate their behavior in soil. Progress and efforts are summarized for each task. Task 1. Production of soluble organo-Cr(III) complexes by selected microorganisms A total of eight organisms were screened for production of soluble organo-Cr(III) complexes by culturing in both growth and non growth media containing 4 mg/L of Cr(VI); three were Gram positive and five were Gram negative. The Gram-positive bacteria were Cellulomonas sp. ES 6, Rhodococcus sp., and Leafsonia sp., while Shewanella oneidensis MR 1, Desulfovibrio desulfuricans G20, D. vulgaris Hildenborough, Pseudomonas putida MK 1 and Ps. aeruginosa PAO 1 were Gram negative. Purifications of the soluble organo-Cr(III) complexes produced by Cellulomonas sp. ES 6, Shewanella. oneidensis MR 1, Rhodococcus sp., and D. vulgaris Hildenborough were carried out. The culture supernatants were lyophilized and extracted first with methanol followed by water. The extracts were then analyzed for soluble Cr. The majority of the Cr(III) was present in the water-soluble fraction for all of the bacteria tested (data not shown), revealing a general phenomenon of soluble Cr(III) production. Cellulomonas sp. ES6 produced the highest amount of soluble Cr(III) (364 ppm) and D. vulgaris Hildenborough produced the least (143 ppm). Seventy eight percent of the soluble Cr(III) produced by Shewanella. oneidensis MR 1 was

  3. Facile synthesis of efficient visible active C-doped TiO{sub 2} nanomaterials with high surface area for the simultaneous removal of phenol and Cr(VI)

    Energy Technology Data Exchange (ETDEWEB)

    Mani, A.Daya; Reddy, P.Manoj Kumar; Srinivaas, M. [Department of Chemistry, IIT Hyderabad, Yeddumailaram 502 205 (India); Ghosal, P., E-mail: csubbu@iith.ac.in [Defence Metallurgical Research Laboratory, Kanchanbagh, Hyderabad 500 058 (India); Xanthopoulos, N. [Ecole Polytechnique Federale de Lausanne (EPFL), Lausanne (Switzerland); Subrahmanyam, Ch. [Department of Chemistry, IIT Hyderabad, Yeddumailaram 502 205 (India)

    2015-01-15

    Highlights: • Facile synthesis of C-doped TiO{sub 2} nanomaterials with high surface area. • Utilization of citric acid and ascorbic acid as fuels based on evolution of gases. • Enhanced visible activity for the oxidation of phenol and reduction of Cr(VI). • Study of simultaneous oxidation of phenol and reduction of Cr(VI) for the first time. • Proposed plausible mechanism for the simultaneous removal of phenol and Cr(VI). - Abstract: A single step synthesis of carbon doped TiO{sub 2} (anatase) nanomaterials have been reported by using combustion synthesis using ascorbic acid and citric acid fuels. X-ray diffraction studies indicated the formation of nanosized anatase titania, whereas, transmission electron microscopy confirmed the formation of nanosized TiO{sub 2} anatase. The carbon doping into TiO{sub 2} matrix was identified by X-ray photoelectron spectroscopy, whereas, thermogravimetric study quantified the carbon doping. Diffuse reflectance UV–vis spectra indicated the band gap of less than 3 eV, a prerequisite for the photocatalytic activity under visible light irradiation. The N{sub 2} adsorption studies revealed the high surface area (upto 290 m{sup 2}/g) of the synthesized photocatalysts. Typical photocatalytic activity data indicated that the simultaneous removal of Cr(VI) and phenol is advantageous than degradation of the individual pollutants.

  4. Elucidating the Molecular Basis and Regulation of Chromium (VI) Reduction by Shewanella oneidensis MR-1 Using Biochemical, Genomic, and Proteomic Approaches

    Energy Technology Data Exchange (ETDEWEB)

    Hettich, Robert L.

    2006-10-30

    Although microbial metal reduction has been investigated intensively from physiological and biochemical perspectives, little is known about the genetic basis and regulatory mechanisms underlying the ability of certain bacteria to transform, detoxify, or immobilize a wide array of heavy metals contaminating DOE-relevant environments. The major goal of this work is to elucidate the molecular components comprising the chromium(VI) response pathway, with an emphasis on components involved in Cr(VI) detoxification and the enzyme complex catalyzing the terminal step in Cr(VI) reduction by Shewanella oneidensis MR-1. We have identified and characterized (in the case of DNA-binding response regulator [SO2426] and a putative azoreductase [SO3585]) the genes and gene products involved in the molecular response of MR-1 to chromium(VI) stress using whole-genome sequence information for MR-1 and recently developed proteomic technology, in particular liquid chromatographymass spectrometry (LC-MS), in conjunction with conventional protein purification and characterization techniques. The proteome datasets were integrated with information from whole-genome expression arrays for S. oneidensis MR-1 (as illustrated in Figure 1). The genes and their encoded products identified in this study are of value in understanding metal reduction and bacterial resistance to metal toxicity and in developing effective metal immobilization strategies.

  5. Enhancing effect of iron on chromate reduction by Cellulomonas flavigena.

    Science.gov (United States)

    Xu, Weihua; Liu, Yunguo; Zeng, Guangming; Li, Xin; Tang, Chunfang; Yuan, Xingzhong

    2005-11-11

    Cr(VI) is considerably toxic and the detoxification of Cr(VI) is of great importance. This study investigated the effect of iron on Cr(VI) reduction by Cellulomonas flavigena. The results demonstrated that addition of FeCl3 or lepidocrocite promoted Cr(VI) reduction, with the reduction ratio of above 90 and 80% achieved, respectively, but addition of hematite did not lead to the increase of reduction ratio, which suggests that the effect of iron on chromate reduction appears different with the diversity of iron-oxides. In this study, the effect of initial Cr(VI) and Fe(III) concentration on Cr(VI) reduction and the change of pH value were also investigated. The reduction ratio increased with the increase of the initial concentration ratio of Fe(III)/Cr(VI). The value of pH gradually increased from 7.0 to around 9.0.

  6. Studies of kinetic of Cr(VI) adsorption in chitosan magnetic particles by radiochemistry method; Estudo da cinetica de adsorcao de Cr(VI) em particulas magneticas de quitosana pelo metodo radioquimico

    Energy Technology Data Exchange (ETDEWEB)

    Rodriguez, Levi S.; Yamaura, Mitiko; Camilo, Ruth L. [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil)]. E-mail: lsrodri@ipen.br; Landgraf, Fernando J.G. [Instituto de Pesquisas Tecnologicas (IPT), Sao Paulo, SP (Brazil)]. E-mail: landgraf@ipt.br

    2005-07-01

    There are a number of processes which are used for remove or recovery metals from waters and waste waters. However, such processes are expensive and sometimes ineffective, especially when metals are present in solution at very low concentrations. Alternative and more efficient processes than ones usually employed are being intensively investigated as sorption. Biosorption of metals is already sufficiently known and its mechanisms have been intensely studied. Therefore, the efficiency and the mechanism of Cr(VI) ions uptake in chitosan magnetic particles obtained by suspension crosslinking technique were studied. These particles were spherical in shape and had a high porosity degree, a low saturation magnetization and a low percentage of swelling. The Cr(VI) ions uptake onto chitosan magnetic particles followed a mechanism of second order, suggesting chemical adsorption. (author)

  7. Unraveling the mechanism responsible for the contrasting tolerance of Synechocystis and Synechococcus to Cr(VI): Enzymatic and non-enzymatic antioxidants

    Energy Technology Data Exchange (ETDEWEB)

    Gupta, Alka [Molecular Biology Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India); Ballal, Anand, E-mail: aballal@barc.gov.in [Molecular Biology Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India); Homi Bhabha National Institute, Training School Complex, Anushakti Nagar, Mumbai 40085 (India)

    2015-07-15

    Highlights: • Cr(VI) accumulation generates higher ROS in Synechocystis than in Synechococcus. • Synechococcus exhibits better photosynthetic activity in response to Cr(VI). • Synechococcus has higher enzymatic/non-enzymatic antioxidants than Synechocystis. • Synechococcus shows better tolerance to other oxidative stresses than Synechocystis. • Differential detoxification of ROS is responsible for the contrasting tolerance to Cr(VI) - Abstract: Two unicellular cyanobacteria, Synechocystis and Synechococcus, showed contrasting tolerance to Cr(VI); with Synechococcus being 12-fold more tolerant than Synechocystis to potassium dichromate. The mechanism responsible for this differential sensitivity to Cr(VI) was explored in this study. Total content of photosynthetic pigments as well as photosynthetic activity decreased at lower concentration of Cr(VI) in Synechocystis as compared to Synechococcus. Experiments with {sup 51}Cr showed Cr to accumulate intracellularly in both the cyanobacteria. At lower concentrations, Cr(VI) caused excessive ROS generation in Synechocystis as compared to that observed in Synechococcus. Intrinsic levels of enzymatic antioxidants, i.e., superoxide dismutase, catalase and 2-Cys-peroxiredoxin were considerably higher in Synechococcus than Synechocystis. Content of total thiols (both protein as well as non-protein) and reduced glutathione (GSH) was also higher in Synechococcus as compared to Synechocystis. This correlated well with higher content of carbonylated proteins observed in Synechocystis than Synechococcus. Additionally, in contrast to Synechocystis, Synechococcus exhibited better tolerance to other oxidative stresses like high intensity light and H{sub 2}O{sub 2}. The data indicate that the disparity in the ability to detoxify ROS could be the primary mechanism responsible for the differential tolerance of these cyanobacteria to Cr(VI)

  8. Proposta de uma tecnologia ambientalmente sustentável para o tratamento de efluentes de indústrias galvânicas contendo Cr(VI)

    OpenAIRE

    Tiele Caprioli Machado

    2015-01-01

    O cromo hexavalente – Cr(VI) – presente nos efluentes das indústrias galvânicas, entre outras, é tóxico para maioria dos micro-organismos e potencialmente danoso para a saúde humana. No presente trabalho se estuda a redução de Cr(VI) pelos processos fotoquímicos com álcoois e fotocatálise heterogênea, primeiramente em um reator batelada, com objetivo de obter o melhor processo para aplicação industrial. Na sequência, foram realizados experimentos com efluente industrial, contendo Cr(VI), prov...

  9. Formation of freestanding ZrO{sub 2} nanotubes for Cr(VI) removal

    Energy Technology Data Exchange (ETDEWEB)

    Bashirom, Nurulhuda, E-mail: nurulhuda.usm2014@gmail.com; Ye, Beh Chin, E-mail: cyebeh@gmail.com; Razak, Khairunisak Abdul, E-mail: khairunisak@usm.my; Lockman, Zainovia, E-mail: zainovia@usm.my [School of Materials & Mineral Resources Engineering, Universiti Sains Malaysia, 14300 Seri Ampangan, Nibong Tebal, Seberang Prai Selatan, Pulau Pinang (Malaysia)

    2016-07-06

    Freestanding ZrO{sub 2} nanotubes (ZNTs) were produced using a simple anodization method in fluorinated ethylene glycol electrolyte containing 1 ml 1 M K{sub 2}CO{sub 3}. The pH of the bath was kept constant at 8. The potassium carbonate (K{sub 2}CO{sub 3}) was added into electrolyte to promote the detachment of anodic ZrO{sub 2} film from the underlying zirconium (Zr) substrate. The poor adherence of ZNTs layer was due to generation of CO{sub 2} gas that was thought to occur between metal|oxide interfaces. The effect of anodization voltages towards the detachment of ZNTs layer was systematically studied at 20 V, 40 V, 50 V and 60 V for 1 hour. The formation of CO{sub 2} gas is a function of anodization voltage, in which at 60 V, a good anodic film separation seen due to higher formation of CO{sub 2} gas. A preliminary study shown the capability of ZNTs in removing 5 ppm of Cr(VI) aqueous solution under illumination of UV light.

  10. Geophysical monitoring of hydrological and biogeochemical transformations associated with Cr(VI) bioremediation.

    Science.gov (United States)

    Hubbard, Susan S; Williams, Ken; Conrad, Mark E; Faybishenko, Boris; Peterson, John; Chen, Jinsong; Long, Phil; Hazent, Terry

    2008-05-15

    Understanding how hydrological and biogeochemical properties change over space and time in response to remedial treatments is hindered by our ability to monitor these processes with sufficient resolution and over field relevant scales. Here, we explored the use of geophysical approaches for monitoring the spatiotemporal distribution of hydrological and biogeochemical transformations associated with a Cr(VI) bioremediation experiment performed at Hanford, WA. We first integrated hydrological wellbore and geophysical tomographic data sets to estimate hydrological zonation at the study site. Using results from laboratory biogeophysical experiments and constraints provided by field geochemical data sets, we then interpreted time-lapse seismic and radar tomographic data sets, collected during thirteen acquisition campaigns over a three year experimental period, in terms of hydrological and biogeochemical transformations. The geophysical monitoring data sets were used to infer: the spatial distribution of injected electron donor; the evolution of gas bubbles; variations in total dissolved solids (nitrate and sulfate) as a function of pumping activity; the formation of precipitates and dissolution of calcites; and concomitant changes in porosity. Although qualitative in nature, the integrated interpretation illustrates how geophysical techniques have the potential to provide a wealth of information about coupled hydrobiogeochemical responses to remedial treatments in high spatial resolution and in a minimally invasive manner. Particularly novel aspects of our study include the use of multiple lines of evidence to constrain the interpretation of a long-term, field-scale geophysical monitoring data set and the interpretation of the transformations as a function of hydrological heterogeneity and pumping activity.

  11. Aqueous Complexation Reactions Governing the Rate and Extent of Biogeochemical U(VI) Reduction

    Energy Technology Data Exchange (ETDEWEB)

    Scott C. Brooks; Wenming Dong; Sue Carroll; James K. Fredrickson; Kenneth M. Kemner; Shelly D. Kelly

    2006-06-01

    The proposed research will elucidate the principal biogeochemical reactions that govern the concentration, chemical speciation, and reactivity of the redox-sensitive contaminant uranium. The results will provide an improved understanding and predictive capability of the mechanisms that govern the biogeochemical reduction of uranium in subsurface environments. In addition, the work plan is designed to: (1) Generate fundamental scientific understanding on the relationship between U(VI) chemical speciation and its susceptibility to biogeochemical reduction reactions. (2) Elucidate the controls on the rate and extent of contaminant reactivity. (3) Provide new insights into the aqueous and solid speciation of U(VI)/U(IV) under representative groundwater conditions.

  12. Aqueous Complexation Reactions Governing the Rate and Extent of Biogeochemical U(VI) Reduction

    Energy Technology Data Exchange (ETDEWEB)

    Scott C. Brooks; Wenming Dong; Sue Carroll; Jim Fredrickson; Ken Kemner; Shelly Kelly

    2006-06-01

    The proposed research will elucidate the principal biogeochemical reactions that govern the concentration, chemical speciation, and reactivity of the redox-sensitive contaminant uranium. The results will provide an improved understanding and predictive capability of the mechanisms that govern the biogeochemical reduction of uranium in subsurface environments. In addition, the work plan is designed to: (1) Generate fundamental scientific understanding on the relationship between U(VI) chemical speciation and its susceptibility to biogeochemical reduction reactions. ? Elucidate the controls on the rate and extent of contaminant reactivity. (2) Provide new insights into the aqueous and solid speciation of U(VI)/U(IV) under representative groundwater conditions.

  13. Alkaline hydrothermal stabilization of Cr(VI) in soil using glass and aluminum from recycled municipal solid wastes.

    Science.gov (United States)

    Gattullo, Concetta Eliana; D'Alessandro, Caterina; Allegretta, Ignazio; Porfido, Carlo; Spagnuolo, Matteo; Terzano, Roberto

    2018-02-15

    Hexavalent chromium was stabilized in soil by using a mixture of glass and aluminum recovered from municipal solid wastes under alkaline hydrothermal conditions. Cr(VI) concentration was reduced by 94-98% already after 7days of treatment. After the same period, more than 90% of total Cr was stabilized in highly recalcitrant and scarcely mobile chemical forms, with 50% in the residual fraction (when the samples were treated at 1/10w/w mixture/soil ratio). Longer treatments increased Cr stabilization. X-ray microanalyses revealed that Cr was stabilized in geopolymeric structures within large aluminosilicate mineral aggregates (containing both amorphous and crystalline phases). 3D microstructural analyses showed a limited compaction of the soil with still a 20% internal porosity in the neoformed aggregates. Increased pH and salinity after the treatment can be restored by simple soil amendments and washing. Copyright © 2017. Published by Elsevier B.V.

  14. The synthesis of novel thiol/amino bifunctionalized SBA-15 and application on the Cr(VI) absorption

    Science.gov (United States)

    Yang, Y.; Wang, D.; Yang, J. X.

    2017-08-01

    Novel amino/thiol organic groups modified SBA-15 materials were successfully prepared by a simple co-condensation approach. The synthesize mesoporous materials were characterized by FT-IR, SAXRD, N2 adsorption and elemental analysis (EA). The absorption behavior of Cr (VI) in the samples has been investigated. The experiments revealed that the adsorption amount of Cr (VI) was decided by thiol groups, but the adsorption equilibrium time was mainly effected by amino groups. The 15% NH2+20%SH sample had the best adsorption performance. Its maximum adsorption capacity can be up to 49.29 mg/g at the optimum conditions. The research of adsorption mechanism including adsorption kinetics and adsorption thermodynamics was also presented.

  15. Cr(VI Removal from Aqueous by Adsorption on Amine-Functionalized Mesoporous Silica Prepared from Silica Fume

    Directory of Open Access Journals (Sweden)

    Xitong Li

    2014-01-01

    Full Text Available Amino-functionalized mesoporous silica MCM-41 materials have been prepared to develop efficient adsorbents of Cr(VI in wastewater, using silica fume as silica source. Functionalization with amino groups has been carried out by using grafting method. The materials have been characterized by means of X-ray diffraction (XRD, nitrogen (N2 adsorption-desorption, Fourier transform infrared (FTIR spectroscopy, scanning electron microscopy (SEM, transmission electron microscopy (TEM, and X-ray photoelectron spectroscopy (XPS. Adsorption potential of the material for Cr(VI removal from aqueous solution was investigated by varying experimental conditions such as pH, initial metal concentration, and contact time. The equilibrium data were analyzed using the Langmuir and Freundlich isotherm by linear regression analysis, and the results show that the adsorption equilibrium data obeyed the Langmuir model. In addition, the kinetics analysis revealed that the overall adsorption process was successfully fitted with the pseudo-second-order kinetic model.

  16. BIOSORPSI ION LOGAM Cr(VI) DENGAN MENGGUNAKAN BIOMASSA LAMUN Enhalus acoroides YANG TERDAPAT DI PULAU BARRANG LOMPO

    OpenAIRE

    La Nafie, N; Taba, P; Mahmud, D

    2009-01-01

    J Akta Kimia Ind 2(2) 2009 Biosorption is an alternative technique which can be used in solving environmental pollution coming from waste containing heavy metals. Biosorption of Cr(VI) ion using biomass of seagrass, Thalassia hemprichii at various contact time, pH and concentration has been investigated. Biosorption was performed by a batch method and concentration of ions before and after biosorption were measured by atomic absorption spectrophotometer (AAS). The equilibriu...

  17. Determination of Hexavalent Chromium (Cr(VI Concentrations via Ion Chromatography and UV-Vis Spectrophotometry in Samples Collected from Nacogdoches Wastewater Treatment Plant, East Texas (USA

    Directory of Open Access Journals (Sweden)

    Kefa K. Onchoke

    2016-01-01

    Full Text Available The concentration of hexavalent chromium (Cr(VI, a toxic environmental pollutant and carcinogen, was determined in samples collected from Nacogdoches Wastewater Treatment Plant (NWWTP using ion chromatography and UV-visible spectrophotometry (IC, UV-Vis. On reaction with 1,5-diphenylcarbazide (DPC Cr+6 forms a 1,5-diphenylcarbazide-Cr(VI complex, which is then analyzed at 530 nm and 540 nm, respectively. Via ion chromatography Cr(VI concentrations were in the range of 0.00190±0.0020 and 0.0010±0.0006 ppm at the influent and effluent, respectively. With the use of standard addition wastewater samples were spiked with a 0.5 ppm Cr(VI standard of various amounts and subsequently analyzed with UV-Vis spectrophotometry. The spiked concentrations gave Cr(VI concentrations in the range of 0.0090±0.0060 ppm and 0.0040±0.0061 ppm at the influent and influent wastewater, respectively. The determined Cr(VI concentrations through the ion chromatography and UV-Vis spectrophotometry are below the maximum USEPA contaminant concentration of 0.1 ppm. From the analysis, the NWWTP efficiently removes Cr(VI before discharge into the environment through La Nana Creek. The removal efficiency for Cr(VI was determined to be ≥92.8% along the wastewater treatment stages from the influent (aeration stage to the effluent stages prior to discharge into the La Nana Creek.

  18. Effect of seasonality and Cr(VI) on starch-sucrose partitioning and related enzymes in floating leaves of Salvinia minima.

    Science.gov (United States)

    Rosa, Mariana; Prado, Carolina; Chocobar-Ponce, Silvana; Pagano, Eduardo; Prado, Fernando

    2017-09-01

    Effects of seasonality and increasing Cr(VI) concentrations on leaf starch-sucrose partitioning, sucrose- and starch-related enzyme activities, and carbon allocation toward leaf development were analyzed in fronds (floating leaves) of the floating fern Salvinia minima. Carbohydrates and enzyme activities of Cr-exposed fronds showed different patterns in winter and summer. Total soluble sugars, starch, glucose and fructose increased in winter fronds, while sucrose was higher in summer ones. Starch and soluble carbohydrates, except glucose, increased under increasing Cr(VI) concentrations in winter fronds, while in summer ones only sucrose increased under Cr(VI) treatment. In summer fronds starch, total soluble sugars, fructose and glucose practically stayed without changes in all assayed Cr(VI) concentrations. Enzyme activities related to starch and sucrose metabolisms (e.g. ADPGase, SPS, SS and AI) were higher in winter fronds than in summer ones. Total amylase and cFBPase activities were higher in summer fronds. Cr(VI) treatment increased enzyme activities, except ADPGase, in both winter and summer fronds but no clear pattern changes were observed. Data of this study show clearly that carbohydrate metabolism is differently perturbed by both seasonality and Cr(VI) treatment in summer and winter fronds, which affects leaf starch-sucrose partitioning and specific leaf area (SLA) in terms of carbon investment. Copyright © 2017 Elsevier Masson SAS. All rights reserved.

  19. Macromolecule oxidation and DNA repair in mussel (Mytilus edulis L.) gill following exposure to Cd and Cr(VI)

    Energy Technology Data Exchange (ETDEWEB)

    Emmanouil, C. [School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom); Sheehan, T.M.T. [Regional Toxicology Laboratory, City Hospital, Dudley Road, Birmingham B18 7QH (United Kingdom); Chipman, J.K. [School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom)]. E-mail: J.K.Chipman@bham.ac.uk

    2007-04-20

    The oxidation of DNA and lipid was analysed in the marine mussel (Mytilus edulis) in response to exposure (10 {mu}g/l and 200 {mu}g/l) to cadmium (Cd) and chromium [Cr(VI)]. Concentration dependent uptake of both metals into mussel tissues was established and levels of gill ATP were not depleted at these exposure levels. DNA strand breakage in gill cells (analysed by the comet assay) was elevated by both metals, however, DNA oxidation [measured by DNA strand breakage induced by the DNA repair enzyme formamidopyrimidine glycosylase (FPG)] was not elevated. This was despite a statistically significant increase in both malondialdehyde and 4-hydroxynonenal - indicative of lipid peroxidation - following treatment with Cd. In contrast, both frank DNA stand breaks and FPG-induced DNA strand breaks (indicative of DNA oxidation) were increased following injection of mussels with sodium dichromate (10.4 {mu}g Cr(VI)/mussel). The metals also showed differential inhibitory potential towards DNA repair enzyme activity with Cd exhibiting inhibition of DNA cutting activity towards an oligonucleotide containing 8-oxo-7,8-dihydro-2'-deoxyguanosine and Cr(VI) showing inhibition of such activity towards an oligonucleotide containing ethenoadenosine, both at 200 {mu}g/l. The metals thus show DNA damage activity in mussel gill with distinct mechanisms involving both direct and indirect (oxidative) DNA damage, as well as impairing different DNA repair capacities. A combination of these activities can contribute to adverse effects in these organisms.

  20. Studies on biosorption of Cr(VI) on a green resin: dry cow dung powder and tracer technique

    Energy Technology Data Exchange (ETDEWEB)

    Barot, N.S.; Bagla, H.K. [Kishinchand Chellaram College, Mumbai (India). Nuclear and Radiochemistry Dept.

    2012-07-01

    The present investigation entails the application of dry cow dung powder (DCP) as an indigenous, inexpensive and eco-friendly material for the removal of Cr(VI) from aqueous medium. Batch biosorption experiments were conducted employing {sup 51}Cr(VI) as a tracer and the effect of various process parameters such as optimum pH, temperature, amount of resin, time of equilibration, agitation speed, concentration of metal ions and interfering effect of different salts etc. were studied. The kinetic studies were carried out employing various models but the best fitting was given by Lagergren Pseudo-second order model with high correlation coefficient R{sup 2} value of 0.997 and adsorption capacity of 10.20 mg/g. The thermodynamic parameters for biosorption were evaluated as {Delta}G = -2.837 kJ/mol, {Delta}H = -4.757 kJ/mol and {Delta}S = 16.64 J/mol K, which indicated spontaneous and exothermic process with high affinity of DCP for Cr(VI). Many naturally available materials are used for the biosorption of heavy metal pollutants, where most of them are physically or chemically modified. In this research work, DCP has been utilized without any pre or post chemical treatment. Thus it manifests the principle of green chemistry and proves to be an eco-friendly resin. (orig.)

  1. Box-Behnken methodology for Cr (VI) and leather dyes removal by an eco-friendly biosorbent: F. vesiculosus.

    Science.gov (United States)

    Cobas, M; Sanromán, M A; Pazos, M

    2014-05-01

    This study focused on leather industrial effluents treatment by biosorption using Fucus vesiculosus as low-cost adsorbent. These effluents are yellowish-brown color and high concentration of Cr (VI). Therefore, biosorption process was optimized using response surface methodology based on Box-Behnken design operating with a simulated leather effluent obtained by mixture of Cr (VI) solution and four leather dyes. The key variables selected were initial solution pH, biomass dosage and CaCl2 concentration in the pretreatment stage. The statistical analysis shows that pH has a negligible effect, being the biomass dosage and CaCl2 concentration the most significant variables. At optimal conditions, 98% of Cr (VI) and 88% of dyes removal can be achieved. Freundlich fitted better to the obtained equilibrium data for all studied systems than Temkin, Langmuir or D-R models. In addition, the use of the final biosorbent as support-substrate to grown of enzyme producer fungi, Pleurotus ostreatus, was also demonstrated. Copyright © 2014 Elsevier Ltd. All rights reserved.

  2. Enhanced remediation of Cr(VI)-contaminated soil by incorporating a calcined-hydrotalcite-based permeable reactive barrier with electrokinetics.

    Science.gov (United States)

    Zhang, Jia; Xu, Yunfeng; Li, Wentao; Zhou, Jizhi; Zhao, Jun; Qian, Guangren; Xu, Zhi Ping

    2012-11-15

    This paper describes the enhanced Cr(VI)-contaminated soil remediation via a combination of electrokinetics (EK) with a calcined-hydrotalcite-based permeable reactive barrier (PRB). First, this combination proved to be feasible, and remarkably facilitated Cr(VI) remediation in a column test. Then, lightly-to-severely (0.16-1.65 mg/g) Cr(VI)-contaminated soil was remediated in a simulated test with the calcined hydrotalcite as the PRB under an voltage of 10-30 V (i.e. an electric field intensity of 0.7-2.0 V/cm). The observations demonstrated that both PRB and EK are critical to efficient remediation and the high de-contamination efficiency is supposedly attributed to the synergistic effect, for which EK concentrates anionic chromate to the anode region and PRB media (calcined hydrotalcite) absorbs and immobilizes it. Thus we have shown that the combined PRB-EK system is highly adaptive and effective in remediation of a larger area contaminated with chromate and various anionic pollutants. Copyright © 2012 Elsevier B.V. All rights reserved.

  3. The effects of welding parameters on ultra-violet light emissions, ozone and CrVI formation in MIG welding.

    Science.gov (United States)

    Dennis, J H; Mortazavi, S B; French, M J; Hewitt, P J; Redding, C R

    1997-01-01

    This paper describes the relationships between ultra-violet emission, ozone generation and CrVI production in MIG welding which were measured as a function of shield gas flow rate, welding voltage, electrode stick-out and shield gas composition using an automatic welding rig that permitted MIG welding under reproducible conditions. The experimental results are interpreted in terms of the physico-chemical processes occurring in the micro- and macro-environments of the arc as part of research into process modification to reduce occupational exposure to ozone and CrVI production rates in MIG welding. We believe the techniques described here, and in particular the use of what we have termed u.v.-ozone measurements, will prove useful in further study of ozone generation and CrVI formation and may be applied in the investigation of engineering control of occupational exposure in MIG and other welding process such as Manual Metal Arc (MMA) and Tungsten Inert Gas (TIG).

  4. A Water-Stable Luminescent ZnIIMetal-Organic Framework as Chemosensor for High-Efficiency Detection of CrVI-Anions (Cr2O72-and CrO42-) in Aqueous Solution.

    Science.gov (United States)

    Yao, Zhao-Quan; Li, Guang-Yu; Xu, Jian; Hu, Tong-Liang; Bu, Xian-He

    2017-12-06

    A new luminescent Zn II -MOF with 1D triangular channels along the b axis, namely NUM-5, has been successfully assembled and well characterized, which features good stability, especially in aqueous solution. Interestingly, this compound exhibits a fast, sensitive and selective luminescence quenching response towards Cr VI (Cr 2 O 7 2- /CrO 4 2- ) in aqueous solution. The detection limits towards Cr 2 O 7 2- and CrO 4 2- ions are estimated to be 0.7 and 0.3 ppm, respectively, which are among the lowest detection limits reported for the MOF-based fluorescent probes that can simultaneously detect Cr 2 O 7 2- and CrO 4 2- in aqueous environment. The possible detection mechanism has been discussed in detail. Moreover, it can be easily regenerated after detection experiments, indicative of excellent recyclability. All these results suggest NUM-5 to be a highly selective and recyclable luminescent sensing material for the quantitative detection of Cr VI anions in aqueous solution. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  5. Comparative toxicogenomic analysis of oral Cr(VI) exposure effects in rat and mouse small intestinal epithelia

    Energy Technology Data Exchange (ETDEWEB)

    Kopec, Anna K. [Department of Biochemistry and Molecular Biology, Center for Integrative Toxicology, Michigan State University, East Lansing, MI 48824 (United States); Thompson, Chad M. [ToxStrategies, Inc., Katy, TX 77494 (United States); Kim, Suntae; Forgacs, Agnes L. [Department of Biochemistry and Molecular Biology, Center for Integrative Toxicology, Michigan State University, East Lansing, MI 48824 (United States); Zacharewski, Timothy R., E-mail: tzachare@msu.edu [Department of Biochemistry and Molecular Biology, Center for Integrative Toxicology, Michigan State University, East Lansing, MI 48824 (United States)

    2012-07-15

    Continuous exposure to high concentrations of hexavalent chromium [Cr(VI)] in drinking water results in intestinal tumors in mice but not rats. Concentration-dependent gene expression effects were evaluated in female F344 rat duodenal and jejunal epithelia following 7 and 90 days of exposure to 0.3–520 mg/L (as sodium dichromate dihydrate, SDD) in drinking water. Whole-genome microarrays identified 3269 and 1815 duodenal, and 4557 and 1534 jejunal differentially expressed genes at 8 and 91 days, respectively, with significant overlaps between the intestinal segments. Functional annotation identified gene expression changes associated with oxidative stress, cell cycle, cell death, and immune response that were consistent with reported changes in redox status and histopathology. Comparative analysis with B6C3F1 mouse data from a similarly designed study identified 2790 differentially expressed rat orthologs in the duodenum compared to 5013 mouse orthologs at day 8, and only 1504 rat and 3484 mouse orthologs at day 91. Automated dose–response modeling resulted in similar median EC{sub 50}s in the rodent duodenal and jejunal mucosae. Comparative examination of differentially expressed genes also identified divergently regulated orthologs. Comparable numbers of differentially expressed genes were observed at equivalent Cr concentrations (μg Cr/g duodenum). However, mice accumulated higher Cr levels than rats at ≥ 170 mg/L SDD, resulting in a ∼ 2-fold increase in the number of differentially expressed genes. These qualitative and quantitative differences in differential gene expression, which correlate with differences in tissue dose, likely contribute to the disparate intestinal tumor outcomes. -- Highlights: ► Cr(VI) elicits dose-dependent changes in gene expression in rat intestine. ► Cr(VI) elicits less differential gene expression in rats compared to mice. ► Cr(VI) gene expression can be phenotypically anchored to intestinal changes. ► Species

  6. Statistical optimization of process parameters for the simultaneous adsorption of Cr(VI) and phenol onto Fe-treated tea waste biomass

    Science.gov (United States)

    Gupta, Ankur; Balomajumder, Chandrajit

    2017-06-01

    In this study, simultaneous removal of Cr(VI) and phenol from binary solution was carried out using Fe-treated tea waste biomass. The effect of process parameters such as adsorbent dose, pH, initial concentration of Cr(VI) (mg/L), and initial concentration of phenol (mg/L) was optimized. The analysis of variance of the quadratic model demonstrates that the experimental results are in good agreement with the predicted values. Based on experimental design at an initial concentration of 55 mg/L of Cr(VI), 27.50 mg/L of phenol, pH 2.0, 15 g/L adsorbent dose, 99.99% removal of Cr(VI), and phenol was achieved.

  7. Iron Corrosion Observations: Pu(VI)-Fe Reduction Studies

    Energy Technology Data Exchange (ETDEWEB)

    Reed, Donald T. [Los Alamos National Laboratory; Swanson, Juliet S. [Los Alamos National Laboratory; Richmann, Michael K. [Los Alamos National Laboratory; Lucchini, Jean-Francois [Los Alamos National Laboratory; Borkowski, Marian [Los Alamos National Laboratory

    2012-09-11

    Iron and Pu Reduction: (1) Very different appearances in iron reaction products were noted depending on pH, brine and initial iron phase; (2) Plutonium was associated with the Fe phases; (3) Green rust was often noted at the higher pH; (4) XANES established the green rust to be an Fe2/3 phase with a bromide center; and (5) This green rust phase was linked to Pu as Pu(IV).

  8. A new method for separation and determination of Cr(III) and Cr(VI) in water samples by high-performance liquid chromatography based on anion exchange stationary phase of ionic liquid modified silica.

    Science.gov (United States)

    Sadeghi, Susan; Moghaddam, Ali Zeraatkar

    2015-12-01

    In this work, N-methylimidazolium-chloride ionic liquid functionalized silica was prepared and used as an anion-exchange stationary phase for separation of chromium species by high-performance liquid chromatography (HPLC) with UV detection at 200 nm. The Cr(VI) as HCr2O7(-) and chelated Cr(III) with potassium hydrogen phthalate (PHP) as Cr(PHP)2 (-) was retained on the prepared column and separated using a mobile phase composed of 5% methanol in 25 mM phosphate buffer at pH 6.5. Several variables affecting the chelation/separation steps were modeled by response surface methodology (RSM) using Box-Behnken (BBD) design. The significance of the independent variables and their interactions were tested by the analysis of variances (ANOVA) with 95% confidence limit. Under the optimized conditions, the Cr(III) and Cr(VI) anionic species were well separated with a single peak for each Cr species at retention times of 2.3 and 4.3 min, respectively. The relationship between the peak area and concentration was linear in the range of 0.025-30 for Cr(III) and 0.5-20 mg L(-1) for Cr(VI) with detection limits of 0.010 and 0.210 mg L(-1) for Cr(III) and Cr(VI), respectively. The proposed method was validated by simultaneous separation and determination of the Cr species in tap and underground water samples without impose to any pretreatment.

  9. Biosorption of Cr(VI) by Ceratocystis paradoxa MSR2 Using Isotherm Modelling, Kinetic Study and Optimization of Batch Parameters Using Response Surface Methodology

    Science.gov (United States)

    Ramalingam, Chidambaram

    2015-01-01

    This study is focused on the possible use of Ceratocystis paradoxa MSR2 native biomass for Cr(VI) biosorption. The influence of experimental parameters such as initial pH, temperature, biomass dosage, initial Cr(VI) concentration and contact time were optimized using batch systems as well as response surface methodology (RSM). Maximum Cr(VI) removal of 68.72% was achieved, at an optimal condition of biomass dosage 2g L−1, initial Cr(VI) concentration of 62.5 mg L−1 and contact time of 60 min. The closeness of the experimental and the predicted values exhibit the success of RSM. The biosorption mechanism of MSR2 biosorbent was well described by Langmuir isotherm and a pseudo second order kinetic model, with a high regression coefficient. The thermodynamic study also revealed the spontaneity and exothermic nature of the process. The surface characterization using FT-IR analysis revealed the involvement of amine, carbonyl and carboxyl groups in the biosorption process. Additionally, desorption efficiency of 92% was found with 0.1 M HNO3. The Cr(VI) removal efficiency, increased with increase in metal ion concentration, biomass concentration, temperature but with a decrease in pH. The size of the MSR2 biosorbent material was found to be 80 μm using particle size analyzer. Atomic force microscopy (AFM) visualizes the distribution of Cr(VI) on the biosorbent binding sites with alterations in the MSR2 surface structure. The SEM-EDAX analysis was also used to evaluate the binding characteristics of MSR2 strain with Cr(VI) metals. The mechanism of Cr(VI) removal of MSR2 biomass has also been proposed. PMID:25822726

  10. Hexavalent chromium [Cr(VI)] removal by the electrochemical ion-exchange process.

    Science.gov (United States)

    Dharnaik, Amit Shivputra; Ghosh, Pranab Kumar

    2014-01-01

    In the present investigation, the performance of a laboratory-scale plate and frame-type electrochemical ion-exchange (EIX) cell on removal ofhexavalent chromium from synthetic wastewater containing 5 mg/l of Cr(VI) was evaluated under varying applied voltages. Ruthenium dioxide-coated titanium plate (RuO2/Ti) was used as anode and stainless steel plates as cathode. The EIX cell was run at different hydraulic retention time (HRT). Before using in the electrochemical cell, the capacity of ion-exchange resin was evaluated through kinetic and isotherm equilibrium tests in batch mode. The batch kinetic study result showed that the equilibrium time for effective ion exchange with resin is 2 h. The isotherm equilibrium data fit well to both Freundlich and Langmuir isotherms. Maximum capacity (qm) of resin calculated from Langmuir isotherm was 71.42 mg/g. Up to 99% of chromium removal was noticed in the EIX cell containing fresh resin at applied voltages of 10 V and higher. Migration of chromium ion to anode chamber was not noticed while performing the experiment with fresh resin. As high as 50% removal of chromium was observed from the middle chamber containing exhausted resin at an applied voltage of 25 V when the influent flow rate was maintained at 45 min of HRT. The performance of the reactor was increased to 72% when the influent flow rate was decreased to maintain at 90 min of HRT. Build-up of chromium in the anode chamber took place when exhausted resin was used in the process.

  11. Proteomic analysis of chromium stress and sulfur deficiency responses in leaves of two canola (Brassica napus L.) cultivars differing in Cr(VI) tolerance.

    Science.gov (United States)

    Yıldız, Mustafa; Terzi, Hakan

    2016-02-01

    Sulfur (S) is an essential macronutrient for plant growth and development, and it plays an essential role in response to environmental stresses. Plants suffer with combined stress of S deficiency and hexavalent chromium [Cr(VI)] in the rhizosphere. Little is known about the impact of S deficiency on leaf metabolism of canola (Brassica napus L.) under Cr(VI) stress. Therefore, this study is the first to examine the effects of Cr(VI) stress and S deficiency in canola at a molecular level. A comparative proteomic approach was used to investigate the differences in protein abundance between Cr-tolerant NK Petrol and Cr-sensitive Sary cultivars. The germinated seeds were grown hydroponically in S-sufficient (+S) nutrient solution for 7 days and then subjected to S-deficiency (-S) for 7 days. S-deficient and +S seedlings were then exposed to 100μM Cr(VI) for 3 days. Protein patterns analyzed by two-dimensional electrophoresis (2-DE) revealed that 58 protein spots were differentially regulated by Cr(VI) stress (+S/+Cr), S-deficiency (-S/-Cr) and combined stress (-S/+Cr). Of these, 39 protein spots were identified by MALDI-TOF/TOF mass spectrometry. Differentially regulated proteins predominantly had functions not only in photosynthesis, but also in energy metabolism, stress defense, protein folding and stabilization, signal transduction, redox regulation and sulfur metabolism. Six stress defense related proteins including 2-Cys peroxiredoxin BAS1, glutathione S-transferase, ferritin-1, l-ascorbate peroxidase, thiazole biosynthetic enzyme and myrosinase-binding protein-like At3g16470 exhibited a greater increase in NK Petrol. The stress-related proteins play an important role in the detoxification of Cr(VI) and maintaining cellular homeostasis under variable S nutrition. Copyright © 2015 Elsevier Inc. All rights reserved.

  12. Selective and sensitive speciation analysis of Cr(VI) and Cr(III), at sub-μgL-1 levels in water samples by electrothermal atomic absorption spectrometry after electromembrane extraction.

    Science.gov (United States)

    Tahmasebi, Zeinab; Davarani, Saied Saeed Hosseiny

    2016-12-01

    In this work, electromembrane extraction in combination with electrothermal atomic absorption spectrometry (ET-AAS) was investigated for speciation, preconcentration and quantification of Cr(VI) and Cr(III) in water samples through the selective complexation of Cr(VI) with 1,5-diphenylcarbazide (DPC) as a complexing agent. DPC reduces Cr(VI) to Cr(III) ions and then Cr(III) species are extracted based on electrokinetic migration of their cationic complex (Cr(III)-DPC) toward the negative electrode placed in the hollow fiber. Also, once oxidized to Cr(VI), Cr(III) ions in initial sample were determined by this procedure. The influence of extraction parameters such as pH, type of organic solvent, chelating agent concentration, stirring rate, extraction time and applied voltage were evaluated following a one-at-a-time optimization approach. Under optimized conditions, the extracted analyte was quantified by ETAAS, with an acceptable linearity in the range of 0.05-5ngmL-1 (R2 value=0.996), and a repeatability (%RSD) between 3.7% and 12.2% (n=4) for 5.0 and 1.0ngmL-1 of Cr(VI), respectively. Also, we obtained an enrichment factor of 110 that corresponded to the recovery of 66%. The detection limit (S/N ratio of 3:1) was 0.02ngmL-1. Finally, this new method was successfully employed to determine Cr(III) and Cr(VI) species in real water samples. Copyright © 2016. Published by Elsevier B.V.

  13. Toxic effect of Cr(VI) in presence of n-TiO2 and n-Al2O3 particles towards freshwater microalgae.

    Science.gov (United States)

    Dalai, Swayamprava; Pakrashi, Sunandan; Bhuvaneshwari, M; Iswarya, V; Chandrasekaran, N; Mukherjee, Amitava

    2014-01-01

    The reactivity and toxicity of the soluble toxicants in the presence of the engineered nanomaterials is not well explored. In this study, the probable effects of TiO2 and Al2O3 nanoparticles (n-TiO2, n-Al2O3) on the toxicity of Cr(VI) were assessed with the dominant freshwater algae, Scenedesmus obliquus, in a low range of exposure concentrations (0.05, 0.5 and 1μg/mL). In the presence of 0.05μg/mL n-TiO2, the toxicity of Cr(VI) decreased considerably, which was presumably due to the Cr(VI) adsorption on the nanoparticle surface leading to its aggregation and precipitation. The elevated n-TiO2 concentrations (0.5 and 1μg/mL) did not significantly influence Cr(VI) bio-availability, and a dose dependent toxicity of Cr(VI) was observed. On the other hand, n-Al2O3 did not have any significant effect on the Cr(VI) toxicity. The microscopic observations presented additional information on the morphological changes of the algal cells in the presence of the binary toxicants. The generation of reactive oxygen species (ROS) suggested contribution of oxidative stress on toxicity and LDH release confirmed membrane permeability of algal cells upon stress. Copyright © 2013 Elsevier B.V. All rights reserved.

  14. Chemodynamics of chromium reduction in soils: Implications to bioavailability

    Energy Technology Data Exchange (ETDEWEB)

    Choppala, Girish [Centre for Environmental Risk Assessment and Remediation, Building-X, University of South Australia, Mawson Lakes, South Australia 5095 (Australia); Cooperative Research Centre for Contamination Assessment and Remediation of the Environment, PO Box 486, Salisbury, South Australia 5106 (Australia); Bolan, Nanthi, E-mail: Nanthi.Bolan@unisa.edu.au [Centre for Environmental Risk Assessment and Remediation, Building-X, University of South Australia, Mawson Lakes, South Australia 5095 (Australia); Cooperative Research Centre for Contamination Assessment and Remediation of the Environment, PO Box 486, Salisbury, South Australia 5106 (Australia); Seshadri, Balaji [Centre for Environmental Risk Assessment and Remediation, Building-X, University of South Australia, Mawson Lakes, South Australia 5095 (Australia); Cooperative Research Centre for Contamination Assessment and Remediation of the Environment, PO Box 486, Salisbury, South Australia 5106 (Australia)

    2013-10-15

    Highlights: • Examined the effects of sorption, pH and C sources on Cr(VI) reduction and toxicity. • The rate of Cr(VI) reduction decreased with an increase in Cr(VI) adsorption and pH. • The proton dynamics in Cr(VI) reduction was assessed in relation to remediation. • A novel black carbon showed the highest reduction rate of Cr(VI) in soils. • Black carbon decreased the bioavailability and phytotoxicity of Cr(VI) in soils. -- Abstract: Chromium toxicity in soils can be mitigated by reduction of Cr(VI) to Cr(III) which is influenced by the presence of free Cr(VI) species in soil solution, and the supply of protons and electrons. In this study, the effects of Cr(VI) adsorption (i.e. availability of free Cr(VI) species in soil solution), soil pH (i.e. supply of protons) and three electron donor carbon sources [black carbon (BC), chicken manure biochar (CMB) and cow manure (CM)] on the reduction of Cr(VI) to Cr(III) in soils were investigated. The results indicated that the rate of Cr(VI) reduction decreased with an increase in Cr(VI) adsorption and soil pH, which is attributed to decreased supply of free Cr(VI) ions and protons, respectively. Among the three different amendments tested, BC showed the highest rate of Cr(VI) reduction followed by CM and CMB. Furthermore, addition of BC, CM and CMB decreased the bioavailability of Cr(VI) in contaminated soils. The high efficiency of BC on Cr(VI) reduction was due to the electron donor's functional groups such as phenolic, hydroxyl, carbonyl and amides. The study demonstrated that free form of Cr(VI) ions in soil solution and carbon amendments enriched with acidic functional groups favored the reduction of Cr(VI), thereby mitigating its bioavailability and toxicity in contaminated soils.

  15. Efeito da toxicidade de Cr (VI e Zn (II no crescimento do fungo filamentoso Aspergillus niger isolado de efluente industrial Toxicity effect of Cr (VI and Zn (II on growth of filamentous fungi Aspergillus niger isolated from industrial effluent

    Directory of Open Access Journals (Sweden)

    Maria do Socorro Vale

    2011-09-01

    Full Text Available Processos convencionais de tratamento de efluentes utilizam microrganismos vivos, o que sugere limitações relativas À toxicidade de metais para os microrganismos. O experimento consistiu em adicionar soluções monoelementares de Cr (VI e Zn(II em diferentes concentrações (0, 20, 50, 100, 200, 300, 400, 500 mg.L-1 ao meio de crescimento e observar a influência dos metais no crescimento micelial e germinativo do fungo Aspergillus Níger por verificação visual da expansão radial do micélio e da germinação de esporos, seguida de registro fotográfico. Os resultados mostraram que o metabolismo do fungo foi completamente inibido em concentrações acima de 500 mg Zn (II.L-1 e 150 mg Cr (VI.L-1. O ED50 (concentração de ingrediente ativo capaz de inibir 50% do crescimento micelial do fungo para os dois íons metálicos, nas condições estudadas, está na faixa entre 100 e 150 mg.L-1. Palavras-chave: metais pesados; inibição; crescimento micelial; Aspergillus niger; ED50.Many standard processes of wastewater treatment use live microorganisms, which suggests limitations on a metal toxicity to the microorganism. The experiment consisted in adding mono elementary solutions of Cr (VI and Zn (II at different concentrations (0, 20, 50, 100, 200, 300, 400, 500 mg.L-1 to the growth mean, and to observe the influence of metals on mycelial and germinative growth of the Aspergillus niger fungus, by means of visual observation of the radial expansion of the mycelius and the germination of spores, followed by photograph registration. The results showed that the metabolism of the fungus was completely inhibited at concentrations above 500 mg Zn (II.L-1 and 150 mg Cr (VI.L-1. The ED50 (concentration of active ingredient capable of inhibiting 50% of mycelial growth of the fungus for both metal ions, under the studied conditions, is in the range between 100 and 150 mg.L-1.

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