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  • 2005-2009  (4)
  • Geography  (4)
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  • 2005-2009  (4)
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  • Geography  (4)
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  • 1
    Online Resource
    Online Resource
    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
    Abstract: 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.
    Type of Medium: Online Resource
    ISSN: 0361-5995 , 1435-0661
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2006
    detail.hit.zdb_id: 241415-6
    detail.hit.zdb_id: 2239747-4
    detail.hit.zdb_id: 196788-5
    detail.hit.zdb_id: 1481691-X
    SSG: 13
    SSG: 21
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Online Resource
    Online Resource
    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
    Abstract: 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.
    Type of Medium: Online Resource
    ISSN: 0361-5995 , 1435-0661
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2006
    detail.hit.zdb_id: 241415-6
    detail.hit.zdb_id: 2239747-4
    detail.hit.zdb_id: 196788-5
    detail.hit.zdb_id: 1481691-X
    SSG: 13
    SSG: 21
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Online Resource
    Online Resource
    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
    Abstract: 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
    Type of Medium: Online Resource
    ISSN: 0361-5995 , 1435-0661
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2006
    detail.hit.zdb_id: 241415-6
    detail.hit.zdb_id: 2239747-4
    detail.hit.zdb_id: 196788-5
    detail.hit.zdb_id: 1481691-X
    SSG: 13
    SSG: 21
    Library Location Call Number Volume/Issue/Year Availability
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  • 4
    Online Resource
    Online Resource
    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
    Abstract: 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.
    Type of Medium: Online Resource
    ISSN: 0361-5995 , 1435-0661
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2008
    detail.hit.zdb_id: 241415-6
    detail.hit.zdb_id: 2239747-4
    detail.hit.zdb_id: 196788-5
    detail.hit.zdb_id: 1481691-X
    SSG: 13
    SSG: 21
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
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