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Effects of humic material on the precipitation of calcium phosphate

机译:腐殖质对磷酸钙沉淀的影响

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Soil organic acids such as humic and fulvic acids can play an important role in influencing inorganic phosphate availability in P-fertilized soils by inhibiting formation of thermodynamically stable calcium phosphates. Calcium phosphate phases which are important in these systems may include amorphous calcium phosphate (Ca-9(PO4)(6).nH(2)O; ACP), dicalcium phosphate dihydrate (CaHPO4.2H(2)O; DCPD, also known as brushite), octacalcium phosphate (Ca8H2(PO4)(6).5H(2)O; OCP) and the thermodynamically most stable phase, hydroxyapatite (Ca-5(PO4)(3)OH; HAp). In this study, the formation of these phases in the presence of soil humic acids derived from the Sydney Basin in New South Wales, Australia has been examined using the combined techniques of pH-stat autotitration, Fourier transform infrared (FTIR) and laser Raman spectroscopy, as well as X-ray diffraction (XRD) and elemental analyses. Under conditions of high supersaturation at a pH of 7.4 and a temperature of 25 degreesC, it was found that these soil humics delay the transformation of unstable ACP to thermodynamically more stable OCP and thence to an apatitic phase resembling poorly crystalline HAp. At the lower pH of 5.7, and in the presence of humic acids, ACP was also precipitated initially. However, this was in contrast to the humic-free solutions which produced DCPD. ACP produced in the presence of humic materials persisted longer than DCPD in their absence, before ultimately hydrolyzing to OCR Modes of humic-calcium phosphate interaction are discussed. It has been concluded that humic materials are geologically relevant inhibitors of calcium phosphate transformation and that they may modify, the availability of phosphorus in soils by changing crystallisation behaviour from solution
机译:土壤有机酸(例如腐殖酸和富里酸)可通过抑制热力学稳定的磷酸钙的形成,在影响磷肥土壤中无机磷酸盐的利用率方面发挥重要作用。在这些系统中重要的磷酸钙相可能包括无定形磷酸钙(Ca-9(PO4)(6).nH(2)O; ACP),磷酸二钙二水合物(CaHPO4.2H(2)O; DCPD作为透钙磷石),磷酸八钙(Ca8H2(PO4)(6).5H(2)O; OCP)和热力学最稳定的相羟基磷灰石(Ca-5(PO4)(3)OH; HAp)。在这项研究中,使用pH值自动滴定,傅立叶变换红外(FTIR)和激光拉曼光谱技术的组合技术,研究了存在于澳大利亚新南威尔士州悉尼盆地的土壤腐殖酸存在下这些相的形成。 ,以及X射线衍射(XRD)和元素分析。发现在pH值为7.4且温度为25摄氏度的条件下具有较高的过饱和度时,发现这些土壤腐殖质延迟了不稳定的ACP向热力学更稳定的OCP的转化,并延迟了其向类似结晶性HAp的脂溶相的转化。在较低的pH值为5.7且存在腐殖酸的情况下,ACP最初也会沉淀。但是,这与产生DCPD的无腐殖酸溶液相反。存在腐殖质的情况下产生的ACP持续存在的时间比不存在腐殖质的情况下的DCPD持续的时间长,最后讨论了腐殖酸与磷酸钙相互作用的OCR模式。得出的结论是,腐殖质是磷酸钙转化的地质相关抑制剂,它们可能通过改变溶液中的结晶行为而改变土壤中磷的有效性。

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