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The interaction of glyphosate with soil constituents.

机译:草甘膦与土壤成分的相互作用。

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摘要

The chemical mechanisms that govern glyphosate interactions with soil constituents are not fully understood. In studies of single soil constituents, iron and aluminum oxides have shown a particularly high affinity for glyphosate compared to other soil constituents. We used goethite and poorly crystalline boehmite (PCB) in this study as model sorbents to show the interactions of glyphosate on soil constituents. We identified glyphosate sorption on goethite and PCB using coupled sorption and Fourier-Transform Infrared (FTIR), high-performance liquid chromatography (HPLC), diffuse reflectance, and in situ attenuated total reflectance (ATR) FTIR measurements.;Glyphosate sorbed strongly to goethite and PCB. The sorption of glyphosate reached a maximum of 133 and 217 mumol/g glyphosate for goethite and PCB, respectively. As the loading of glyphosate increased, the solution pH also increased. The increase in pH suggests that hydroxyl groups were displaced from the sorbent surfaces, thus evidence of ligand exchange.;By using ATR-FTIR and Raman spectroscopy, we found that the phosphonate bands of glyphosate shifted with changes in pH. At pH 3 the protonated P-OH group displayed a band at 917 cm-1, and the symmetric and asymmetric P-OH modes appear at 1080 and 1186 cm-1, respectively. At higher pH values, the P-OH band disappears due to deprotonation of the P-O bond. The POH modes merge and form a single band at 1093 cm-1, which represents the P-O asymmetric stretching mode.;We also compared the spectra of glyphosate in solution with those of glyphosate on the sorbents. We noticed that the sorbent perturbed the phosphonate group of glyphosate. In the presence of goethite and PCB, the phosphonate stretching bands appeared at 1137 and 1107 cm-1, respectively. In solution, this band appeared at 1093 cm-1. The shift of the P-O stretch to a higher frequency when in the presence of the sorbents is evidence for glyphosate binding via its phosphonate moiety.;In an effort to join batch sorption and spectroscopic studies, we also found that the coupled batch sorption and spectroscopic studies showed good agreement concerning the macroscopic sorption behavior of glyphosate on the sorbents. This information, linked with the aforementioned spectroscopic work is significant because it provides further information concerning the binding of glyphosate with the sorbents.
机译:草甘膦与土壤成分相互作用的化学机理尚未完全了解。在研究单一土壤成分时,与其他土壤成分相比,铁和氧化铝对草甘膦的亲和力特别高。在本研究中,我们使用针铁矿和结晶度较差的勃姆石(PCB)作为模型吸附剂,以显示草甘膦与土壤成分的相互作用。我们使用耦合吸附和傅里叶变换红外(FTIR),高效液相色谱(HPLC),漫反射率和原位衰减全反射率(ATR)FTIR测量确定了针铁矿和PCB上的草甘膦吸附;草甘膦强烈吸附到针铁矿上和PCB。对于针铁矿和PCB,草甘膦的吸附量最高分别达到133和217μmol/ g草甘膦。随着草甘膦含量的增加,溶液的pH值也增加。 pH值的增加表明羟基已从吸附剂表面移开,从而证明了配体交换。;通过使用ATR-FTIR和拉曼光谱,我们发现草甘膦的膦酸酯带随pH的变化而移动。在pH为3时,质子化的P-OH基团在917 cm-1处显示出一条带,对称和不对称的P-OH模式分别在1080和1186 cm-1处出现。在较高的pH值下,由于P-O键的去质子作用,P-OH带消失。 POH模式合并并在1093 cm-1处形成一个单一谱带,代表P-O不对称拉伸模式。;我们还比较了溶液中草甘膦的光谱与吸附剂上草甘膦的光谱。我们注意到吸附剂扰乱了草甘膦的膦酸酯基团。在针铁矿和PCB的存在下,膦酸酯拉伸带分别出现在1137和1107 cm-1处。在溶液中,该条带出现在1093 cm-1处。在存在吸附剂的情况下,PO的拉伸移向更高的频率是草甘膦通过其膦酸酯部分结合的证据。;在加入批量吸附和光谱研究的过程中,我们还发现批量吸附和光谱研究相结合与草甘膦在吸附剂上的宏观吸附行为表现出良好的一致性。该信息与上述光谱工作有关,因为它提供了有关草甘膦与吸附剂结合的进一步信息,因此具有重要意义。

著录项

  • 作者

    Johnson, Eric Christopher.;

  • 作者单位

    Purdue University.;

  • 授予单位 Purdue University.;
  • 学科 Agriculture Soil Science.;Chemistry Agricultural.;Environmental Sciences.
  • 学位 M.S.
  • 年度 2009
  • 页码 122 p.
  • 总页数 122
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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