author_facet Baldermann, Andre
Grießbacher, Andrea
Baldermann, Claudia
Purgstaller, Bettina
Letofsky-Papst, Ilse
Kaufhold, Stephan
Dietzel, Martin
Baldermann, Andre
Grießbacher, Andrea
Baldermann, Claudia
Purgstaller, Bettina
Letofsky-Papst, Ilse
Kaufhold, Stephan
Dietzel, Martin
author Baldermann, Andre
Grießbacher, Andrea
Baldermann, Claudia
Purgstaller, Bettina
Letofsky-Papst, Ilse
Kaufhold, Stephan
Dietzel, Martin
spellingShingle Baldermann, Andre
Grießbacher, Andrea
Baldermann, Claudia
Purgstaller, Bettina
Letofsky-Papst, Ilse
Kaufhold, Stephan
Dietzel, Martin
Geosciences
Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents
General Earth and Planetary Sciences
author_sort baldermann, andre
spelling Baldermann, Andre Grießbacher, Andrea Baldermann, Claudia Purgstaller, Bettina Letofsky-Papst, Ilse Kaufhold, Stephan Dietzel, Martin 2076-3263 MDPI AG General Earth and Planetary Sciences http://dx.doi.org/10.3390/geosciences8090309 <jats:p>The capacity and mechanism of the adsorption of aqueous barium (Ba), cobalt (Co), strontium (Sr), and zinc (Zn) by Ecuadorian (NatAllo) and synthetic (SynAllo-1 and SynAllo-2) allophanes were studied as a function of contact time, pH, and metal ion concentration using kinetic and equilibrium experiments. The mineralogy, nano-structure, and chemical composition of the allophanes were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, and specific surface area analyses. The evolution of adsorption fitted to a pseudo-first-order reaction kinetics, where equilibrium between aqueous metal ions and allophane was reached within &lt;10 min. The metal ion removal efficiencies varied from 0.7 to 99.7% at pH 4.0 to 8.5. At equilibrium, the adsorption behavior is better described by the Langmuir model than by the Dubinin–Radushkevich model, yielding sorption capacities of 10.6, 17.2, and 38.6 mg/g for Ba 2 + , 12.4, 19.3, and 29.0 mg/g for HCoO 2 − ; 7.2, 15.9, and 34.4 mg/g for Sr 2 + ; and 20.9, 26.9, and 36.9 mg/g for Zn 2 + , by NatAllo, SynAllo-2, and SynAllo-1, respectively. The uptake mechanism is based on a physical adsorption process rather than chemical ion exchange. Allophane holds great potential to effectively remove aqueous metal ions over a wide pH range and could be used instead of other commercially available sorbent materials such as zeolites, montmorillonite, carbonates, and phosphates for special wastewater treatment applications.</jats:p> Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents Geosciences
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title Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents
title_unstemmed Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents
title_full Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents
title_fullStr Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents
title_full_unstemmed Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents
title_short Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents
title_sort removal of barium, cobalt, strontium, and zinc from solution by natural and synthetic allophane adsorbents
topic General Earth and Planetary Sciences
url http://dx.doi.org/10.3390/geosciences8090309
publishDate 2018
physical 309
description <jats:p>The capacity and mechanism of the adsorption of aqueous barium (Ba), cobalt (Co), strontium (Sr), and zinc (Zn) by Ecuadorian (NatAllo) and synthetic (SynAllo-1 and SynAllo-2) allophanes were studied as a function of contact time, pH, and metal ion concentration using kinetic and equilibrium experiments. The mineralogy, nano-structure, and chemical composition of the allophanes were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, and specific surface area analyses. The evolution of adsorption fitted to a pseudo-first-order reaction kinetics, where equilibrium between aqueous metal ions and allophane was reached within &lt;10 min. The metal ion removal efficiencies varied from 0.7 to 99.7% at pH 4.0 to 8.5. At equilibrium, the adsorption behavior is better described by the Langmuir model than by the Dubinin–Radushkevich model, yielding sorption capacities of 10.6, 17.2, and 38.6 mg/g for Ba 2 + , 12.4, 19.3, and 29.0 mg/g for HCoO 2 − ; 7.2, 15.9, and 34.4 mg/g for Sr 2 + ; and 20.9, 26.9, and 36.9 mg/g for Zn 2 + , by NatAllo, SynAllo-2, and SynAllo-1, respectively. The uptake mechanism is based on a physical adsorption process rather than chemical ion exchange. Allophane holds great potential to effectively remove aqueous metal ions over a wide pH range and could be used instead of other commercially available sorbent materials such as zeolites, montmorillonite, carbonates, and phosphates for special wastewater treatment applications.</jats:p>
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author Baldermann, Andre, Grießbacher, Andrea, Baldermann, Claudia, Purgstaller, Bettina, Letofsky-Papst, Ilse, Kaufhold, Stephan, Dietzel, Martin
author_facet Baldermann, Andre, Grießbacher, Andrea, Baldermann, Claudia, Purgstaller, Bettina, Letofsky-Papst, Ilse, Kaufhold, Stephan, Dietzel, Martin, Baldermann, Andre, Grießbacher, Andrea, Baldermann, Claudia, Purgstaller, Bettina, Letofsky-Papst, Ilse, Kaufhold, Stephan, Dietzel, Martin
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description <jats:p>The capacity and mechanism of the adsorption of aqueous barium (Ba), cobalt (Co), strontium (Sr), and zinc (Zn) by Ecuadorian (NatAllo) and synthetic (SynAllo-1 and SynAllo-2) allophanes were studied as a function of contact time, pH, and metal ion concentration using kinetic and equilibrium experiments. The mineralogy, nano-structure, and chemical composition of the allophanes were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, and specific surface area analyses. The evolution of adsorption fitted to a pseudo-first-order reaction kinetics, where equilibrium between aqueous metal ions and allophane was reached within &lt;10 min. The metal ion removal efficiencies varied from 0.7 to 99.7% at pH 4.0 to 8.5. At equilibrium, the adsorption behavior is better described by the Langmuir model than by the Dubinin–Radushkevich model, yielding sorption capacities of 10.6, 17.2, and 38.6 mg/g for Ba 2 + , 12.4, 19.3, and 29.0 mg/g for HCoO 2 − ; 7.2, 15.9, and 34.4 mg/g for Sr 2 + ; and 20.9, 26.9, and 36.9 mg/g for Zn 2 + , by NatAllo, SynAllo-2, and SynAllo-1, respectively. The uptake mechanism is based on a physical adsorption process rather than chemical ion exchange. Allophane holds great potential to effectively remove aqueous metal ions over a wide pH range and could be used instead of other commercially available sorbent materials such as zeolites, montmorillonite, carbonates, and phosphates for special wastewater treatment applications.</jats:p>
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spelling Baldermann, Andre Grießbacher, Andrea Baldermann, Claudia Purgstaller, Bettina Letofsky-Papst, Ilse Kaufhold, Stephan Dietzel, Martin 2076-3263 MDPI AG General Earth and Planetary Sciences http://dx.doi.org/10.3390/geosciences8090309 <jats:p>The capacity and mechanism of the adsorption of aqueous barium (Ba), cobalt (Co), strontium (Sr), and zinc (Zn) by Ecuadorian (NatAllo) and synthetic (SynAllo-1 and SynAllo-2) allophanes were studied as a function of contact time, pH, and metal ion concentration using kinetic and equilibrium experiments. The mineralogy, nano-structure, and chemical composition of the allophanes were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, and specific surface area analyses. The evolution of adsorption fitted to a pseudo-first-order reaction kinetics, where equilibrium between aqueous metal ions and allophane was reached within &lt;10 min. The metal ion removal efficiencies varied from 0.7 to 99.7% at pH 4.0 to 8.5. At equilibrium, the adsorption behavior is better described by the Langmuir model than by the Dubinin–Radushkevich model, yielding sorption capacities of 10.6, 17.2, and 38.6 mg/g for Ba 2 + , 12.4, 19.3, and 29.0 mg/g for HCoO 2 − ; 7.2, 15.9, and 34.4 mg/g for Sr 2 + ; and 20.9, 26.9, and 36.9 mg/g for Zn 2 + , by NatAllo, SynAllo-2, and SynAllo-1, respectively. The uptake mechanism is based on a physical adsorption process rather than chemical ion exchange. Allophane holds great potential to effectively remove aqueous metal ions over a wide pH range and could be used instead of other commercially available sorbent materials such as zeolites, montmorillonite, carbonates, and phosphates for special wastewater treatment applications.</jats:p> Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents Geosciences
spellingShingle Baldermann, Andre, Grießbacher, Andrea, Baldermann, Claudia, Purgstaller, Bettina, Letofsky-Papst, Ilse, Kaufhold, Stephan, Dietzel, Martin, Geosciences, Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents, General Earth and Planetary Sciences
title Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents
title_full Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents
title_fullStr Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents
title_full_unstemmed Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents
title_short Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents
title_sort removal of barium, cobalt, strontium, and zinc from solution by natural and synthetic allophane adsorbents
title_unstemmed Removal of Barium, Cobalt, Strontium, and Zinc from Solution by Natural and Synthetic Allophane Adsorbents
topic General Earth and Planetary Sciences
url http://dx.doi.org/10.3390/geosciences8090309