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首页> 外文期刊>Journal of biological inorganic chemistry: JBIC: a publication of the Society of Biological Inorganic Chemistry >Can the presence of structural phosphorus help to discriminate between abiogenic and biogenic magnetites?
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Can the presence of structural phosphorus help to discriminate between abiogenic and biogenic magnetites?

机译:结构性磷的存在可以帮助区分生源性磁铁矿和生源性磁铁矿吗?

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The influence of phosphate on the competitive formation of magnetite and lepidocrocite and the properties of magnetite prepared from mixtures of Fe(II) and Fe(III) salts were studied. Products were prepared at 90 ℃ and pH 12.5 (series 1), 50 ℃ and pH 7 (series 2) and 20 ℃ and pH 8 (series 3). The P/Fe atomic ratio in the initial solution ranged from 0 to 3% and the pH was kept at the desired value with NaOH or KOH. Air was used as oxidant in series 2 and 3. All products, which were characterized by X-ray diffraction, transmission electron microscopy, chemical analysis and IR spectroscopy, contained a phase intermediate between magnetite and maghemite (referred to as magnetite in this paper). The products of series 1 consisted only of magnetite at all P/Fe ratios, whereas both magnetite and lepidocrocite formed in series 2 and 3 above a certain P/Fe ratio. On increasing the P/Fe ratio in the initial solution, the magnetite crystals became smaller and more oxidized (i.e. closer to maghemite) and the lepidocrocite/magnetite ratio increased. The P associated with magnetite was partly in the form of occluded P, i.e. non-surface-adsorbed phosphate. IR spectra suggested this P to be structural and occurring as low-symmetry PO4 units. Because abiogenic magnetites produced in various environments incorporate structural P but some well-characterized biogenic magnetites seem to contain no P or be formed in P-poor environments, we hypothesize that natural magnetites containing occluded P are unlikely to be biogenic. However, more studies are needed to discard the presence of P in biogenic magnetites.
机译:研究了磷酸盐对磁铁矿和纤铁矿竞争形成的影响以及由Fe(II)和Fe(III)盐的混合物制备的磁铁矿的性能。在90℃和pH 12.5(系列1),50℃和pH 7(系列2)以及20℃和pH 8(系列3)下制备产品。初始溶液中的P / Fe原子比在0%至3%范围内,并且用NaOH或KOH将pH保持在所需值。空气在系列2和3中用作氧化剂。所有通过X射线衍射,透射电子显微镜,化学分析和IR光谱表征的产品,都含有磁铁矿和磁铁矿之间的中间相(在本文中称为磁铁矿)。 。系列1的产品在所有P / Fe比下仅由磁铁矿组成,而在一定P / Fe比之上的系列2和3形成了磁铁矿和纤铁矿。在初始溶液中增加P / Fe比时,磁铁矿晶体变得更小并且被更多地氧化(即,更接近于磁铁矿),并且纤铁矿/磁铁矿比率增加。与磁铁矿结合的P部分地以被吸附的P的形式存在,即非表面吸附的磷酸盐。红外光谱表明该P具有结构性,并以低对称PO4单元的形式出现。因为在各种环境中产生的非生物磁铁矿都含有结构性P,但是一些特性良好的生物磁铁矿似乎不含P或在贫P环境中形成,因此我们假设含有被P堵塞的天然磁铁矿不太可能是生物磁铁矿。然而,需要更多的研究来丢弃生物磁铁矿中P的存在。

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