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Influence of soil minerals on chromium(VI) reduction by sulfide under anoxic conditions

机译:缺氧条件下土壤矿物对硫化物还原铬(VI)的影响

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The effects of soil minerals on chromate (Cr~(VI)O_4~(2-), noted as Cr(VI)) reduction by sulfide were investigated in the pH range of 7.67 to 9.07 under the anoxic condition. The examined minerals included montmorillonite (Swy-2), illite (IMt-2), kaolinite (KGa-2), aluminum oxide (γ-Al2O3), titanium oxide (TiO2, P-25, primarily anatase), and silica (SiO2). Based on their effects on Cr(VI) reduction, these minerals were categorized into three groups: (i) minerals catalyzing Cr(VI) reduction – illite; (ii) minerals with no effect – Al2O3; and (iii) minerals inhibiting Cr(VI) reduction-kaolinite, montmorillonite, SiO2 and TiO2 . The catalysis of illite was attributed primarily to the low concentration of iron solubilized from the mineral, which could accelerate Cr(VI) reduction by shuttling electrons from sulfide to Cr(VI). Additionally, elemental sulfur produced as the primary product of sulfide oxidation could further catalyze Cr(VI) reduction in the heterogeneous system. Previous studies have shown that adsorption of sulfide onto elemental sulfur nanoparticles could greatly increase sulfide reactivity towards Cr(VI) reduction. Consequently, the observed rate constant, k_(obs), increased with increasing amounts of both iron solubilized from illite and elemental sulfur produced during the reaction. The catalysis of iron, however, was found to be blocked by phenanthroline, a strong complexing agent for ferrous iron. In this case, the overall reaction rate at the initial stage of reaction was pseudo first order with respect to Cr(VI), i.e., the reaction kinetics was similar to that in the homogeneous system, because elemental sulfur exerted no effect at the initial stage prior to accumulation of elemental sulfur nanoparticles. In the suspension of kaolinite, which belonged to group (iii), an inhibitive effect to Cr(VI) reduction was observed and subsequently examined in more details. The inhibition was due to the sorption of elemental sulfur onto kaolinite, which reduced or completely eliminated the catalytic effect of elemental sulfur, depending on kaolinite concentration. This was consistent with the observation that the catalysis of externally added elemental sulfur (50 μM) on Cr(VI) reduction would disappear with a kaolinite concentration of more than 5.0 g/L. In kaolinite suspension, the overall reaction rate law was: -d[Cr(VI)]/dt = k_(obs)[H~+]~2[Cr(VI)][HS~-]~(0.70).
机译:在缺氧条件下,研究了土壤矿物质对硫化物还原铬酸盐(Cr〜(VI)O_4〜(2-),记为Cr(VI))的影响。检查的矿物包括蒙脱石(Swy-2),伊利石(IMt-2),高岭石(KGa-2),氧化铝(γ-Al2O3),氧化钛(TiO2,P-25,主要是锐钛矿)和二氧化硅(SiO2 )。根据它们对Cr(VI)还原的影响,将这些矿物分为三类:(i)催化Cr(VI)还原的矿物–伊利石; (ii)无效的矿物-Al2O3; (iii)抑制Cr(VI)还原的矿物-高岭石,蒙脱石,SiO 2和TiO 2。伊利石的催化作用主要归因于从矿物中溶解的铁的低浓度,这可以通过将电子从硫化物传递到Cr(VI)来加速Cr(VI)的还原。此外,作为硫化物氧化主要产物的元素硫可以进一步催化异质体系中的Cr(VI)还原。先前的研究表明,将硫化物吸附到元素硫纳米颗粒上可以大大提高硫化物对Cr(VI)还原的反应性。因此,观察到的速率常数k_(obs)随着从伊利石中溶解的铁和反应过程中产生的元素硫的含量的增加而增加。然而,发现铁的催化作用被菲咯啉(一种强力的亚铁络合剂)阻断。在这种情况下,反应初始阶段的总反应速率相对于Cr(VI)为伪一级反应,即,反应动力学类似于均相系统,因为元素硫在初始阶段没有作用在元素硫纳米粒子积累之前。在属于(iii)组的高岭石的悬浮液中,观察到了对Cr(VI)还原的抑制作用,随后进行了更详细的研究。抑制作用是由于元素硫吸附在高岭石上,取决于高岭石的浓度,其减少或完全消除了元素硫的催化作用。这与以下观察结果一致:当高岭石浓度超过5.0 g / L时,外部添加的元素硫(50μM)对Cr(VI)还原的催化作用将消失。在高岭石悬浮液中,总反应速率规律为:-d [Cr(VI)] / dt = k_(obs)[H〜+]〜2 [Cr(VI)] [HS〜-]〜(0.70)。

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