-
Je něco špatně v tomto záznamu ?
The role of soil components in synthetic mixtures during the adsorption and speciation changes of Cr(VI): Conjunction of the modeling approach with spectroscopic and isotopic investigations
V. Veselská, H. Šillerová, J. Göttlicher, Z. Michálková, JA. Siddique, S. Číhalová, V. Chrastný, R. Steininger, S. Mangold, M. Komárek,
Jazyk angličtina Země Nizozemsko
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- adsorpce MeSH
- chrom chemie MeSH
- látky znečišťující půdu chemie MeSH
- půda chemie MeSH
- regenerace a remediace životního prostředí * MeSH
- železité sloučeniny chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
This study investigates redox transitions associated with the adsorption of Cr(VI) on commonly occurring soil components (silicates, oxides and humic acids) and their synthetic mixtures by coupling the mechanistic surface complexation modeling with spectroscopic and isotopic analyses. The mixtures of soil components were prepared to reflect the composition of the real anthroposol sample, determined by X-ray Powder Diffraction (XRD), total organic carbon (TOC) measurement and extraction methods. The effect of different initial Cr(VI) concentrations (2×10-2, 5×10-4, 10-4, 10-5, and 10-6M), background electrolyte (10-3, 10-2, and 10-1M KNO3), pH values (3-9), and sorbate/sorbent ratios (2g/L - 20g/L) were investigated. Maghemite and ferrihydrite were confirmed to be the main phases controlling Cr(VI) adsorption with increasing Cr(VI) concentration. Humic acids were primarily responsible for Cr(VI) reduction, especially at low pH values. The reduction of Cr(VI) was also proved in case of illite and kaolinite by XAS and isotopic analyses. Illite revealed higher reduction capacity in comparison with kaolinite based on XAS measurements. Chromium isotopic fractionation, resulting from Cr(VI) reduction, was the highest in the case of humic acids, followed by kaolinite and illite. However, a dissolution of intrinsic Cr originally present within kaolinite and illite might affect the final Cr isotopic composition of the supernatants due to its different Cr isotopic signature. In general, the combination of three different approaches was confirmed to offer more comprehensive information about Cr(VI) adsorption and/or reduction in soils. Detailed studies using soil mixtures can help to predict how the soil components affect Cr(VI) behavior in natural soils and possibly could improve the environmental remediation processes.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19044838
- 003
- CZ-PrNML
- 005
- 20200811104428.0
- 007
- ta
- 008
- 200109s2019 ne f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.envint.2019.03.066 $2 doi
- 035 __
- $a (PubMed)31075676
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Veselská, Veronika $u Department of Environmental Geosciences, Faculty of Environmental Sciences, Czech University of Life Sciences Prague, Kamýcká 129, CZ-16500 Prague, Czech Republic. Electronic address: veselskav@fzp.czu.cz.
- 245 14
- $a The role of soil components in synthetic mixtures during the adsorption and speciation changes of Cr(VI): Conjunction of the modeling approach with spectroscopic and isotopic investigations / $c V. Veselská, H. Šillerová, J. Göttlicher, Z. Michálková, JA. Siddique, S. Číhalová, V. Chrastný, R. Steininger, S. Mangold, M. Komárek,
- 520 9_
- $a This study investigates redox transitions associated with the adsorption of Cr(VI) on commonly occurring soil components (silicates, oxides and humic acids) and their synthetic mixtures by coupling the mechanistic surface complexation modeling with spectroscopic and isotopic analyses. The mixtures of soil components were prepared to reflect the composition of the real anthroposol sample, determined by X-ray Powder Diffraction (XRD), total organic carbon (TOC) measurement and extraction methods. The effect of different initial Cr(VI) concentrations (2×10-2, 5×10-4, 10-4, 10-5, and 10-6M), background electrolyte (10-3, 10-2, and 10-1M KNO3), pH values (3-9), and sorbate/sorbent ratios (2g/L - 20g/L) were investigated. Maghemite and ferrihydrite were confirmed to be the main phases controlling Cr(VI) adsorption with increasing Cr(VI) concentration. Humic acids were primarily responsible for Cr(VI) reduction, especially at low pH values. The reduction of Cr(VI) was also proved in case of illite and kaolinite by XAS and isotopic analyses. Illite revealed higher reduction capacity in comparison with kaolinite based on XAS measurements. Chromium isotopic fractionation, resulting from Cr(VI) reduction, was the highest in the case of humic acids, followed by kaolinite and illite. However, a dissolution of intrinsic Cr originally present within kaolinite and illite might affect the final Cr isotopic composition of the supernatants due to its different Cr isotopic signature. In general, the combination of three different approaches was confirmed to offer more comprehensive information about Cr(VI) adsorption and/or reduction in soils. Detailed studies using soil mixtures can help to predict how the soil components affect Cr(VI) behavior in natural soils and possibly could improve the environmental remediation processes.
- 650 _2
- $a adsorpce $7 D000327
- 650 _2
- $a chrom $x chemie $7 D002857
- 650 12
- $a regenerace a remediace životního prostředí $7 D052918
- 650 _2
- $a železité sloučeniny $x chemie $7 D005290
- 650 _2
- $a půda $x chemie $7 D012987
- 650 _2
- $a látky znečišťující půdu $x chemie $7 D012989
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Šillerová, Hana $u Department of Environmental Geosciences, Faculty of Environmental Sciences, Czech University of Life Sciences Prague, Kamýcká 129, CZ-16500 Prague, Czech Republic.
- 700 1_
- $a Göttlicher, Jörg $u Institute for Photon Science and Synchrotron Radiation, Karlsruhe Institute of Technology, Hermann-von-Helmholtz-Platz 1, DE-76344 Eggenstein-Leopoldshafen, Germany.
- 700 1_
- $a Michálková, Zuzana $u Department of Environmental Geosciences, Faculty of Environmental Sciences, Czech University of Life Sciences Prague, Kamýcká 129, CZ-16500 Prague, Czech Republic.
- 700 1_
- $a Siddique, Jamal A $u Department of Environmental Geosciences, Faculty of Environmental Sciences, Czech University of Life Sciences Prague, Kamýcká 129, CZ-16500 Prague, Czech Republic.
- 700 1_
- $a Číhalová, Sylva $u Department of Environmental Geosciences, Faculty of Environmental Sciences, Czech University of Life Sciences Prague, Kamýcká 129, CZ-16500 Prague, Czech Republic. $7 xx0148982
- 700 1_
- $a Chrastný, Vladislav $u Department of Environmental Geosciences, Faculty of Environmental Sciences, Czech University of Life Sciences Prague, Kamýcká 129, CZ-16500 Prague, Czech Republic.
- 700 1_
- $a Steininger, Ralph $u Institute for Photon Science and Synchrotron Radiation, Karlsruhe Institute of Technology, Hermann-von-Helmholtz-Platz 1, DE-76344 Eggenstein-Leopoldshafen, Germany.
- 700 1_
- $a Mangold, Stefan $u Institute for Photon Science and Synchrotron Radiation, Karlsruhe Institute of Technology, Hermann-von-Helmholtz-Platz 1, DE-76344 Eggenstein-Leopoldshafen, Germany.
- 700 1_
- $a Komárek, Michael $u Department of Environmental Geosciences, Faculty of Environmental Sciences, Czech University of Life Sciences Prague, Kamýcká 129, CZ-16500 Prague, Czech Republic.
- 773 0_
- $w MED00001541 $t Environment international $x 1873-6750 $g Roč. 127, č. - (2019), s. 848-857
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31075676 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20200109 $b ABA008
- 991 __
- $a 20200811104424 $b ABA008
- 999 __
- $a ok $b bmc $g 1483107 $s 1083511
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 127 $c - $d 848-857 $e 20190507 $i 1873-6750 $m Environment international $n Environ Int $x MED00001541
- LZP __
- $a Pubmed-20200109