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由光芬顿处理后的废水生成的铁酸盐。

Ferrite formation from photo-Fenton treated wastewater.

机构信息

National Institute of Advanced Industrial Science and Technology (AIST), 16-1, Onogawa, Tsukuba, Ibaraki 305-8506, Japan.

出版信息

Chemosphere. 2010 Jun;80(4):404-9. doi: 10.1016/j.chemosphere.2010.04.023.

Abstract

Photo-Fenton oxidation followed by ferrite formation was applied for the degradation of a representative organic compound, phenol, and the subsequent removal of the Fe ions. At a phenol:Fe(II):H(2)O(2) molar ratio of 1:0.5:15, TOC analysis showed almost complete mineralization of 10.6mM phenol after 2h at a controlled pH of 3. Recalcitrant low molecular weight organic acid by-products particularly oxalic acid were destroyed. A ferrous-rich solution was generated so that alkalinization at pH 10.5 generated a pitch black sludge of lower volume and moisture content than a ferric hydroxide control of the same Fe concentration. The flocs exhibited a strong affinity for a magnet and its X-ray diffraction pattern showed a close similarity to a standard spinel magnetite. With proper monitoring of Fe(II) and dissolved oxygen, the reaction was successfully controlled to generate flocs with more than 30% magnetite content. When photo-Fenton was employed as a pre-treatment step so that residual oxalic acid remained, ferrite formation was not inhibited. The presence of oxalates even allowed ferrites to form in a solution containing Ca(2+) ions, which is well-known to be deterrent to the process.

摘要

光芬顿氧化法随后进行铁酸盐形成,用于降解一种代表性的有机化合物苯酚,并随后去除铁离子。在苯酚:Fe(II):H 2 O 2 的摩尔比为 1:0.5:15,TOC 分析表明,在控制 pH 值为 3 的条件下,2 小时内可完全矿化 10.6mM 苯酚。难降解的低分子量有机酸副产物,特别是草酸,被破坏了。生成富亚铁溶液,在 pH 值为 10.5 时碱化生成的黑色污泥体积和含水量都比相同铁浓度的氢氧化铁控制的污泥要小。絮体对磁铁具有很强的亲和力,其 X 射线衍射图谱与标准尖晶石磁铁矿非常相似。通过对 Fe(II)和溶解氧的适当监测,成功地控制了反应,生成了磁铁矿含量超过 30%的絮体。当光芬顿被用作预处理步骤时,即使残留的草酸,铁酸盐的形成也不会被抑制。即使在含有 Ca(2+)离子的溶液中,草酸的存在也允许铁酸盐形成,这是众所周知的对该过程有抑制作用的。

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