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  • Lang, Friederike  (10)
  • 2005-2009  (10)
Medientyp
Sprache
Erscheinungszeitraum
  • 2005-2009  (10)
Jahr
Fachgebiete(RVK)
  • 1
    Online-Ressource
    Online-Ressource
    Elsevier BV ; 2006
    In:  Geochimica et Cosmochimica Acta Vol. 70, No. 3 ( 2006-2), p. 595-607
    In: Geochimica et Cosmochimica Acta, Elsevier BV, Vol. 70, No. 3 ( 2006-2), p. 595-607
    Materialart: Online-Ressource
    ISSN: 0016-7037
    RVK:
    Sprache: Englisch
    Verlag: Elsevier BV
    Publikationsdatum: 2006
    ZDB Id: 300305-X
    ZDB Id: 1483679-8
    SSG: 13
    SSG: 16,12
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Online-Ressource
    Online-Ressource
    Elsevier BV ; 2006
    In:  Geochimica et Cosmochimica Acta Vol. 70, No. 12 ( 2006-6), p. 2957-2969
    In: Geochimica et Cosmochimica Acta, Elsevier BV, Vol. 70, No. 12 ( 2006-6), p. 2957-2969
    Materialart: Online-Ressource
    ISSN: 0016-7037
    RVK:
    Sprache: Englisch
    Verlag: Elsevier BV
    Publikationsdatum: 2006
    ZDB Id: 300305-X
    ZDB Id: 1483679-8
    SSG: 13
    SSG: 16,12
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Online-Ressource
    Online-Ressource
    Wiley ; 2006
    In:  Soil Science Society of America Journal Vol. 70, No. 5 ( 2006-09), p. 1547-1555
    In: Soil Science Society of America Journal, Wiley, Vol. 70, No. 5 ( 2006-09), p. 1547-1555
    Kurzfassung: Organic coatings on Fe oxides can decrease the accessibility of intraparticle pores for oxyanions like phosphate. We hypothesized that the slow sorption of phosphate to goethite coated with polygalacturonate (PGA) is controlled by the accessibility of external goethite surfaces to phosphate rather than by diffusion of phosphate into micropores (Ø 〈 2 nm). We studied the phosphate sorption kinetics of pure and PGA‐coated goethites that differed in their microporosity (N 2 at 77 K, 46 vs. 31 mm 3 g −1 ). Because drying may affect the structure or surface coverage of PGA, we also tested the effect of freeze‐drying on the slow phosphate sorption. The samples were examined by gas adsorption (N 2 , CO 2 ) and electrophoretic mobility measurements. Phosphate sorption and PGA‐C desorption were studied in batch experiments for 3 wk at pH 5. In PGA‐coated samples, the slow phosphate sorption was independent of micropore volume. Phosphate displaced on average 57% of PGA‐C within 3 wk. Similar to phosphate sorption, the PGA‐C desorption comprised a rapid initial desorption, which was followed by a slow C desorption. Sorption competition between phosphate and presorbed PGA depended on the 〈 10‐nm porosity and the C loading of the adsorbent. The efficacy of phosphate to desorb PGA generally increased after freeze‐drying. We conclude for PGA‐coated goethites that (i) freeze‐drying biased the slow phosphate sorption by changing the structure/surface coverage of PGA, and (ii) within the time frame studied, micropores did not limit the rate of the slow phosphate sorption. Rather, the slow, gradual desorption of PGA and/or the diffusion of phosphate through PGA coatings controlled the slow phosphate sorption to PGA‐coated goethite.
    Materialart: Online-Ressource
    ISSN: 0361-5995 , 1435-0661
    RVK:
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2006
    ZDB Id: 241415-6
    ZDB Id: 2239747-4
    ZDB Id: 196788-5
    ZDB Id: 1481691-X
    SSG: 13
    SSG: 21
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Online-Ressource
    Online-Ressource
    Wiley ; 2007
    In:  Journal of Environmental Quality Vol. 36, No. 4 ( 2007-07), p. 1187-1193
    In: Journal of Environmental Quality, Wiley, Vol. 36, No. 4 ( 2007-07), p. 1187-1193
    Kurzfassung: Drying of soil may increase the hydrophobicity of soil and affect the mobilization of colloids after re‐wetting. Results of previous research suggest that colloid hydrophobicity is an important parameter in controlling the retention of colloids and colloid‐associated substances in soils. We tested the hypothesis that air‐drying of soil samples increases the hydrophobicity of water‐dispersible colloids and whether air‐drying affects the mobilization of colloid‐associated heavy metals. We performed batch experiments with field‐moist and air‐dried (25°C) soils from a former sewage farm (sandy loam), a municipal park (loamy sand), and a shooting range site (loamy sand with 25% C org ). The filtered suspensions ( 〈 1.2 μm) were analyzed for concentrations of dissolved and colloidal organic C and heavy metals (Cu, Cd, Pb, Zn), average colloid size, zeta potential, and turbidity. The hydrophobicity of colloids was determined by their partitioning between a hydrophobic solid and a hydrophilic aqueous phase. Drying increased hydrophobicity of the solid phase but did not affect the hydrophobicity of the dispersed colloids. Drying decreased the amount of mobilized mineral and (organo‐)mineral colloids in the sewage farm soils but increased the mobilization of organic colloids in the C‐rich shooting range soil. Dried samples released less colloid‐bound Cd and Zn than field‐moist samples. Drying‐induced mobilization of dissolved organic C caused a redistribution of Cu from the colloidal to the dissolved phase. We conclude that drying‐induced colloid mobilization is not caused by a change in the physicochemical properties of the colloids. Therefore, it is likely that the mobilization of colloids in the field is caused by increasing shear forces or the disintegration of aggregates.
    Materialart: Online-Ressource
    ISSN: 0047-2425 , 1537-2537
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2007
    ZDB Id: 120525-0
    ZDB Id: 2050469-X
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  • 5
    Online-Ressource
    Online-Ressource
    Elsevier BV ; 2007
    In:  Colloids and Surfaces A: Physicochemical and Engineering Aspects Vol. 303, No. 3 ( 2007-8), p. 249-252
    In: Colloids and Surfaces A: Physicochemical and Engineering Aspects, Elsevier BV, Vol. 303, No. 3 ( 2007-8), p. 249-252
    Materialart: Online-Ressource
    ISSN: 0927-7757
    Sprache: Englisch
    Verlag: Elsevier BV
    Publikationsdatum: 2007
    ZDB Id: 1500517-3
    ZDB Id: 1169792-1
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Online-Ressource
    Online-Ressource
    Wiley ; 2006
    In:  Soil Science Society of America Journal Vol. 70, No. 5 ( 2006-09), p. 1731-1740
    In: Soil Science Society of America Journal, Wiley, Vol. 70, No. 5 ( 2006-09), p. 1731-1740
    Kurzfassung: Uronates are important constituents of maize mucilage and polyuronates are used as a simplified model of the soil–root interface. We tested whether galacturonate (GA) and polygalacturonate (PGA) impair the diffusion of phosphate (PO 4 ) into and out of pores of a synthetic goethite (147 m 2 g −1 ) and whether the effect of maize mucigel (MU) is comparable to PGA. We measured the PO 4 desorption kinetics of goethites in batch experiments over 2 wk at pH 5. One part of the goethite was equilibrated with organic substances before PO 4 addition, another part after addition of PO 4 Before the desorption experiments, the porosity of our samples was analyzed by N 2 gas adsorption. In each treatment a rapid initial desorption was followed by a slow desorption reaction, which is assigned to the diffusion of PO 4 out of mineral pores. No consistent relation between the micro‐ and mesoporosity and the rate of the slow PO 4 desorption was observed. Compared with the C‐free control, only PGA and MU affected the fraction of PO 4 mobilized by the fast and slow desorption reaction: when PGA was sorbed to goethite before PO 4 , twice as much PO 4 was mobilized via the fast reaction than in the treatment where PO 4 was sorbed before PGA, suggesting a decreased accessibility of goethite pores to PO 4 Mucigel, however, showed reversed effects, which is ascribed to its differing chemical composition. In conclusion, PGA seems inappropriate as a model substance for maize MU collected from non‐axenic sand cultures. Under the experimental conditions chosen, the efficacy of all organic substances to increase PO 4 solution concentrations by pore clogging and sorption competition is small.
    Materialart: Online-Ressource
    ISSN: 0361-5995 , 1435-0661
    RVK:
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2006
    ZDB Id: 241415-6
    ZDB Id: 2239747-4
    ZDB Id: 196788-5
    ZDB Id: 1481691-X
    SSG: 13
    SSG: 21
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 7
    Online-Ressource
    Online-Ressource
    Springer Science and Business Media LLC ; 2005
    In:  Plant and Soil Vol. 275, No. 1-2 ( 2005-08), p. vii-vii
    In: Plant and Soil, Springer Science and Business Media LLC, Vol. 275, No. 1-2 ( 2005-08), p. vii-vii
    Materialart: Online-Ressource
    ISSN: 0032-079X , 1573-5036
    Sprache: Englisch
    Verlag: Springer Science and Business Media LLC
    Publikationsdatum: 2005
    ZDB Id: 1478535-3
    ZDB Id: 208908-7
    SSG: 12
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    Online-Ressource
    Online-Ressource
    Wiley ; 2006
    In:  Soil Science Society of America Journal Vol. 70, No. 2 ( 2006-03), p. 541-549
    In: Soil Science Society of America Journal, Wiley, Vol. 70, No. 2 ( 2006-03), p. 541-549
    Kurzfassung: Biogenetic polysugars may affect the sorption characteristics of soil mineral particles in the rhizosphere. We hypothesized that polygalacturonate [PGA, (C 6 H 7 O 6 ) n − ] coatings on goethite reduce the diffusion of phosphate into the pores of the adsorbent. Goethite was preloaded with PGA (0–10 mg C g −1 ). The samples were characterized by N 2 and CO 2 adsorption, electrophoretic mobility measurements, and scanning electron microscopy/energy dispersive X‐ray analysis (SEM‐EDX). The phosphate sorption kinetics was studied with batch experiments over 2 wk at pH 5 and an initial phosphate concentration of 250 μ M Pore volume and specific surface area of the goethite samples declined after PGA addition. The PGA coatings reduced the ζ‐potential of goethite from 42.3 to −39.6 mV at the highest C loading. With increasing PGA‐C content and decreasing ζ‐potential the amount of phosphate sorbed after 2 wk decreased linearly ( P 〈 0.001). Sorption of phosphate to pure and PGA‐coated goethite showed an initial fast sorption followed by a slow sorption reaction. At the smallest C loading (5.5 mg C g −1 ) the portion of phosphate retained by the slow reaction was smaller than for the treatment without any PGA, while at higher C loadings the fraction of slowly immobilized phosphate increased. Our results suggest that at low C‐loadings PGA impaired the intraparticle diffusion of phosphate. In contrast, the slow step‐by‐step desorption of PGA ( 〈 52% within 2 wk) or the diffusion of phosphate through PGA coatings or both are rate limiting for the slow phosphate reaction at C loadings 〉 5.5 mg C g −1
    Materialart: Online-Ressource
    ISSN: 0361-5995 , 1435-0661
    RVK:
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2006
    ZDB Id: 241415-6
    ZDB Id: 2239747-4
    ZDB Id: 196788-5
    ZDB Id: 1481691-X
    SSG: 13
    SSG: 21
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    Online-Ressource
    Online-Ressource
    Wiley ; 2008
    In:  Soil Science Society of America Journal Vol. 72, No. 6 ( 2008-11), p. 1694-1707
    In: Soil Science Society of America Journal, Wiley, Vol. 72, No. 6 ( 2008-11), p. 1694-1707
    Kurzfassung: Proton nuclear magnetic resonance ( 1 H NMR) relaxometry has been used to analyze pore size distributions of wet porous samples. To make this method applicable to soil samples, knowledge about contribution from the soil solution to the total proton relaxation is needed. We extracted soil solutions from nine soil samples and determined transverse proton relaxation rates, the concentration of Fe, Mn, and total organic C (TOC), and the pH of the solutions. The effects of Fe, Mn, and TOC on the proton relaxation in the soil solution were compared with those of dissolved Fe 2+ , Fe 3+ , and Mn 2+ and of glucose, d ‐cellobiose, potassium hydrogen phthalate, sodium alginate, and agar in model solutions. Proton relaxation rates in the soil solutions were up to 20 times larger than in pure water, which was mainly due to dissolved Fe(III) and Mn(II) species. The relaxivities of Fe and Mn in soil solution were reduced to 40 and 70% compared with Fe(III) and Mn(II) in a model solution, respectively. Smaller relaxivities were primarily due to the formation of metal–organic complexes. We conclude that the proton relaxation in soil samples is generally accelerated by the soil solution, and its contribution must be considered to estimate pore sizes from relaxation times. By using the calculated relaxivities of Fe and Mn in soil solution, the contribution of the soil solution to the total proton relaxation can be estimated from the Fe and Mn concentration in the soil solution.
    Materialart: Online-Ressource
    ISSN: 0361-5995 , 1435-0661
    RVK:
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2008
    ZDB Id: 241415-6
    ZDB Id: 2239747-4
    ZDB Id: 196788-5
    ZDB Id: 1481691-X
    SSG: 13
    SSG: 21
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 10
    Online-Ressource
    Online-Ressource
    Wiley ; 2009
    In:  Journal of Environmental Quality Vol. 38, No. 3 ( 2009-05), p. 933-939
    In: Journal of Environmental Quality, Wiley, Vol. 38, No. 3 ( 2009-05), p. 933-939
    Kurzfassung: Liming is a common technique suggested for the stabilization of shooting range sites. We investigated the effect of an increase in pH on the mobilization of soluble and dispersible (colloidal) Pb, As, and Sb. Our hypothesis was that the addition of divalent cations counteracts the pH‐induced mobilization of soluble and colloidal metal(loid)s. We determined soluble (operationally defined as the fraction 〈 10 nm obtained after centrifugation) and dispersible (filter cut‐off 1200 nm) As, Pb, Sb, Fe, and C org concentrations in the filtered suspensions of batch extracts of topsoil samples (C org : 8%) from a former shooting range site following a pH increase to values between 3.5 and 7 by adding a monovalent (KOH) or a divalent (Ca(OH) 2 ) base. In the Ca(OH) 2 –treated samples, dissolved metal(loid) concentrations were 62 to 98% lower than those titrated with KOH to similar pH. Similarly, Ca reduced the concentration of dispersible Pb by 95%, but had little or no impact on dispersible As and Sb. We conclude that the counterion valency controls the mobility of metal(loid)s by affecting the mobility and sorption capacity of the sorbents (e.g., colloids, organic matter).
    Materialart: Online-Ressource
    ISSN: 0047-2425 , 1537-2537
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2009
    ZDB Id: 120525-0
    ZDB Id: 2050469-X
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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