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  • ENERGY PRODUCTION AND CONVERSION  (4)
  • exchangeable Ca  (3)
  • 1
    ISSN: 1573-0867
    Keywords: Anion exchange resin ; Bray 1 ; cation exchange resin ; Colwell ; exchangeable Ca ; P dissolution ; P fractionation ; P sorption capacity ; P tests ; Phosphate rocks ; Olsen ; Truog
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The objective of this work was to develop and evaluate a soil test suitable for estimating the phosphorus status of soils whether they were fertilized with soluble or sparingly soluble P fertilizers or both. Four New Zealand soils of contrasting P sorption capacity and exchangeable Ca content were incubated alone or with monocalcium phosphate (MCP), reactive North Carolina (NC) phosphate rock or unreactive Florida (FRD) rock, at 240 mg P kg−1 soil, to allow the P sources of different solubilities to react with each soil and provide soil samples containing different amounts of extractable P, Ca and residual phosphate rock. The phosphorus in the incubated soils was fractionated into alkali soluble and acid soluble P fractions using a sequential extraction procedure to assess the extent of phosphate rock dissolution. Eight soil P tests [three moderately alkaline — Olsen (0.5M NaHCO3) modified Olsen (pretreatment with 1M NaCl) and Colwell; three acid tests — Bray 1, modified Bray 1 and Truog; and two resin tests — bicarbonate anion exchange resin (AER) and combined AER plus sodium cation exchange resin (CER)] were assessed in their ability to extract P from the incubated soils. The 0.5M NaHCO3 based alkaline tests could not differentiate between the Control and FRD treatments in any soil nor between the Control, NC and FRD treatments in the high P sorption soils. The acid extractants appeared to be affected by the P sorption capacity of the soil probably because of reabsorption of dissolved P in the acid medium. The AER test gave results similar to Olsen. Only the combined AER + CER test extracted P in amounts related to the solubility of the P sources incubated with each soil. Furthermore, when soil samples were “spiked” with FRD and NC and extracted immediately, the P extracted by the AER + CER test, over and above the control soils, increased with the amount and chemical reactivity of the rocks. There was no extraction of rock P by any of the alkaline extractions. Increases in the amounts of P extracted (ΔP) by each soil test from the fertilized soils, over and above the control soils were compared with the amounts ofP dissolved from the fertilizers during incubation (measured by P fractionation). Soil P sorption capacity had least influence on the amounts of P extracted by the AER + CER and Colwell tests. However, the Colwell test was unable to differentiate between all P sources in all four soils and suffered from the disadvantage of producing coloured extracts. The AER + CER test appeared to have the potential to assess the available P status of soils better than the other tests used because of its ability to extract a representative portion of residual PR (in accordance with the amount and reactivity) and dissolved P, and thus to differentiate between fertilizer treatments in all four soils.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Nutrient cycling in agroecosystems 24 (1990), S. 173-180 
    ISSN: 1573-0867
    Keywords: Phosphate ; resin beads ; resin membranes ; resin-strips ; anion exchange resin ; cation exchange resin ; P sorption capacity ; exchangeable Ca ; phosphate rocks
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract A simplified procedure for determining the amount of phosphate (P) extracted from soils by ion exchange resin membranes is reported. Strips of anion (HCO 3 - form) and cation (Na+ form) exchange membrane were shaken with suspensions of soil in deionised water for 16–17 hours. After shaking, the strips were thoroughly rinsed in deionised water before the phosphate retained on the anion exchange resin strip was determined by shaking the strip directly with phosphate reagent. Compared to the common use of resin beads in nylon mesh bags, this resin membrane procedure is simpler, more convenient, and because an elution step is omitted, less time consuming. The mixed resin membrane method for soil phosphate extraction was compared to the use of resin bags on four New Zealand soils, contrasting in P sorbing capacity and exchangeable calcium. The soils were preincubated with and without 240 mg P kg−1 soil with three P sources of different solubilities. The resin strips extracted amounts of P which were closely correlated (R2 = 0.972) with that extracted by the resin bags. The amounts of P extracted by the mixed resin procedure were in proportion to the solubility of the P sources in each soil.
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  • 3
    ISSN: 1573-0867
    Keywords: Dry matter yield ; exchangeable Ca ; phosphate rocks ; P sorption capacity ; relative agronomic effectiveness ; substitution ratio
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Six phosphate rocks (PRs) of varying reactivities were compared with monocalcium phosphate (MCP) in a glasshouse experiment growing perennial ryegrass (Lolium perenne cv. Nui) as the test plant on four soils of contrasting P sorption capacity and exchangeable Ca. The cumulative dry matter yield over 10 harvests showed a significant response to P application in all soils. Based on relative yield and P uptake, MCP was the most effective P fertilizer followed by the reactive phosphate rocks, which were superior to the unreactive rocks in all soils. The relative agronomic effectiveness (RAE) and substitution ratio (SR) of individual PR fertilizers, calculated with respect to MCP using the methods of ‘vertical’ and ‘horizontal’ comparison, respectively, were similar over a range of fertilizer rate. There was a decline or slight increase in the performance of PRs with time in the low P sorption soils but a consistent increase in the high P sorption soils. Some initial influence of exchangeable Ca content of the soils on the relative performance of PRs was also observed. Generally the PRs performed better in high P sorption soils than low P sorption soils and in low exchangeable Ca soils than high exchangeable Ca soils.
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  • 4
    Publication Date: 2011-08-24
    Description: Two experimental techniques - equilibrium or reversible cell discharge and measurement of open circuit potential as a function of temperature - are used to determine the thermodynamic data needed to estimate the heat generation characteristics of Li/BCX and Li/SOCl2 cells. The results obtained showed that the reversible cell potential, the temperature dependence of the reversible cell potential, and the thermoneutral potential of the BCX cell were 3.74 V, -0.857 +/- 0.198 mV/K, and 3.994 +/- 0.0603 V, respectively. The respective values obtained for the Li/SOCl2 cell were 3.67 V, -0.776 +/- 0.255 mV/K, and 3.893 +/- 0.0776 V. The difference between the thermoneutral potential of Li/BCX and Li/SCl2 cells is attributable to the difference in their electroactive components.
    Keywords: ENERGY PRODUCTION AND CONVERSION
    Type: Electrochemical Society, Journal (ISSN 0013-4651); 139; 9, Se
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  • 5
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    In:  Other Sources
    Publication Date: 2011-08-24
    Description: The mathematical model developed by Sunu and Bennion has been extended to include the separator, precipitation of both solid ZnO and K2Zn(OH)4, and the air electrode, and has been used to investigate the behavior of a primary Zn-Air battery with respect to battery design features. Predictions obtained from the model indicate that anode material utilization is predominantly limited by depletion of the concentration of hydroxide ions. The effect of electrode thickness on anode material utilization is insignificant, whereas material loading per unit volume has a great effect on anode material utilization; a higher loading lowers both the anode material utilization and delivered capacity. Use of a thick separator will increase the anode material utilization, but may reduce the cell voltage.
    Keywords: ENERGY PRODUCTION AND CONVERSION
    Type: Electrochemical Society, Journal (ISSN 0013-4651); 139; 1105-111
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  • 6
    Publication Date: 2019-07-12
    Description: A two-dimensional thermal model for spirally wound batteries has been developed. The governing equation of the model is the energy balance. Convective and insulated boundary conditions are used, and the equations are solved using a finite element code called TOPAZ2D. The finite element mesh is generated using a preprocessor to TOPAZ2D called MAZE. The model is used to estimate temperature profiles within a spirally wound D-size cell. The model is applied to the lithium/thionyl chloride cell because of the thermal management problems that this cell exhibits. Simplified one-dimensional models are presented that can be used to predict best and worst temperature profiles. The two-dimensional model is used to predict the regions of maximum temperature within the spirally wound cell. Normal discharge as well as thermal runaway conditions are investigated.
    Keywords: ENERGY PRODUCTION AND CONVERSION
    Type: Electrochemical Society, Journal (ISSN 0013-4651); 136; 2145-215
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  • 7
    Publication Date: 2019-08-28
    Description: A two-dimensional and time-dependent thermal model of a multicell common pressure vessel (CPV) nickel-hydrogen battery was developed. A finite element solver called PDE/Protran was used to solve this model. The model was used to investigate the effects of various design parameters on the temperature profile within the cell. The results were used to help find a design that will yield an acceptable temperature gradient inside a multicell CPV nickel-hydrogen battery. Steady-state and unsteady-state cases with a constant heat generation rate and a time-dependent heat generation rate were solved.
    Keywords: ENERGY PRODUCTION AND CONVERSION
    Type: Electrochemical Society, Journal (ISSN 0013-4651); 139; 10; p. 2781-2787.
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