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Dissolution kinetics of pyroaurite-type layered double hydroxide doped with Zn: Perspectives for pH controlled micronutrient release

机译:Zn掺杂焦铁矿型层状双氢氧化物的溶解动力学:pH值控制微量营养素释放的前景

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摘要

Layered double hydroxides (LDH) have a high potential for use as a source of micronutrients for plants since their dissolution rates may be controlled within the pH range observed in rhizospheres of plants in need of nutrients. Here the Zn2+ release from a pyroaurite-type LDH host at different pH was investigated. Zinc doped Mg-Fe(III) LDH intercalated with nitrate (PY(Zn)(NO3)) was synthesized by co-precipitation. For reference, both the nitrate and carbonate forms without Zn doping (PYNO3 and PYCO3) were also synthesized. The LDH with a Mg:Fe(III) molar ratio of 2 were found to be pure. LDH dissolution was monitored at a constant pH (4-8) to study the release of framework metal cations, dissolution stoichiometry and release kinetics. The LDH dissolved incongruently, releasing Mg2+ and Zn2+, and leaving an Fe(III)-enriched residue. The stoichiometry of metal release at a particular pH remained the same throughout the dissolution. Release kinetics of Zn2+ and Mg2+ from PY LDH was 'first order' with respect to the metal cations in the LDH, providing rate constants in the range of 0.16 x 10(-3) to 10.1 x 10(-3) min(-1), with the highest rate constants at low pH. Metal ion (M) release had a fractional order with respect to [H+], resulting in overall release kinetics according to: rate = k(H) x [M][H+](n) with n in the range 0.25-0.43. The type of interlayer anion did not affect the overall release kinetics. Lower amounts of Zn2+ were released with respect to Mg2+ as pH increased, indicating that Zn2+ was increasingly retained in the residual Fe(III)-enriched phase. The present study demonstrates not only the pH-controlled release of micronutrient metal cations doped into the LDH framework but also points to resorption as critical parameters for optimizing the release profile. Furthermore, the present study indicates how the incorporation of the desired metal cation within the structure of the LDH may be adapted for other micronutrient/s such as Mn or Cu with the intention of using them as fertilizer. (C) 2016 Elsevier B.V. All rights reserved.
机译:层状双氢氧化物(LDH)具有很高的潜力,可以用作植物微量营养素的来源,因为它们的溶解速度可以控制在需要营养的植物根际中观察到的pH范围内。在此研究了在不同pH下从焦铁石型LDH主体释放的Zn2 +。通过共沉淀法合成了掺有硝酸盐(PY(Zn)(NO3))的掺杂锌的Mg-Fe(III)LDH。作为参考,还合成了没有锌掺杂的硝酸盐和碳酸盐形式(PYNO3和PYCO3)。发现Mg:Fe(III)摩尔比为2的LDH是纯净的。在恒定的pH(4-8)下监测LDH的溶出度,以研究骨架金属阳离子的释放,溶出化学计量和释放动力学。 LDH溶解不均匀,释放Mg2 +和Zn2 +,并留下富含Fe(III)的残留物。在整个溶解过程中,特定pH下金属释放的化学计量保持不变。相对于LDH中的金属阳离子,PY LDH中Zn2 +和Mg2 +的释放动力学为``一级'',提供的速率常数范围为0.16 x 10(-3)至10.1 x 10(-3)min(-1) ),在低pH下具有最高的速率常数。金属离子(M)的释放相对于[H +]具有分数阶,从而导致整体释放动力学根据:速率= k(H)x [M] [H +](n),n在0.25-0.43的范围内。层间阴离子的类型不影响整体释放动力学。随着pH值的增加,相对于Mg2 +释放出的Zn2 +含量更低,这表明Zn2 +越来越多地保留在残留的Fe(III)富集相中。本研究表明,不仅pH控释了掺杂到LDH骨架中的微量元素金属阳离子的释放,而且还指出了将吸收作为优化释放曲线的关键参数。此外,本研究表明在LDH结构中所需金属阳离子的掺入如何适用于其他微量元素,如Mn或Cu,以用作肥料。 (C)2016 Elsevier B.V.保留所有权利。

著录项

  • 来源
    《Applied clay science》 |2016年第4期|56-63|共8页
  • 作者单位

    Univ Copenhagen, Dept Plant & Environm Sci, Thorvaldsensvej 40, DK-1871 Frederiksberg C, Denmark;

    Univ Copenhagen, Dept Plant & Environm Sci, Thorvaldsensvej 40, DK-1871 Frederiksberg C, Denmark;

    Univ Copenhagen, Dept Plant & Environm Sci, Thorvaldsensvej 40, DK-1871 Frederiksberg C, Denmark;

    Univ Copenhagen, Dept Plant & Environm Sci, Thorvaldsensvej 40, DK-1871 Frederiksberg C, Denmark;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Layered double hydroxide (LDH); Micronutrients; Dissolution; Release kinetics;

    机译:层状双氢氧化物(LDH);微量元素;溶解;释放动力学;

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