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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Kinetics, surface chemistry, and structural evolution of microbially mediated sulfide mineral dissolution
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Kinetics, surface chemistry, and structural evolution of microbially mediated sulfide mineral dissolution

机译:微生物介导的硫化物矿物溶解的动力学,表面化学和结构演变

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摘要

The effects of different microbial populations on the oxidative dissolution of sulfide minerals at 37 degreesC and pH 1.5 were examined over a period of 22 days. Samples of pyrite, marcasite, and arsenopyrite were exposed to a sulfur-oxidizing isolate (Thiobacillus caldus), an iron-oxidizing isolate (Ferroplasma acidarmanus), and a mixed enrichment culture containing T. caldus. F. acidarmanus, and Leptospirillum ferrooxidans dans. Changes in chemical speciation of the mineral surface products were monitored by Raman spectroscopy over the course of the experiment. structural evolution was examined with scanning electron microscopy, and the total soluble iron was used as a measure of the dissolution rate. In the case of all three minerals, an increase in dissolution rate was observed only in the presence of iron-oxidizing microorganisms (i.e., F. acidarmanus or the enrichment culture). The chemical speciation at the mineral surface in the presence of these iron-oxidizing species is indistinguishable from that of abiotic control reactions under the same conditions; both are dominated by elemental sulfur. In contrast, experiments with T. caldus indicate that the quantity of elemental sulfur on the mineral surface is <1% of the amount observed on samples exposed to the F. acidarmanus culture. It is surprising that removal of the elemental sulfur from the mineral surface by the sulfur-oxidizing species is nor accompanied by an increase in the dissolution rate of the mineral. This finding suggests that although elemental sulfur forms on the surface during oxidative dissolution, it does not passivate the mineral surface. Copyright (C) 2001 Elsevier Science Ltd. [References: 48]
机译:在22天的时间内检查了不同微生物种群对37°C和pH 1.5的硫化物矿物氧化溶解的影响。将黄铁矿,镁铁矿和毒砂的样品暴露于硫氧化分离株(卡尔德氏硫杆菌),铁氧化分离株(酸铁质费拉氏菌)和含有卡尔德氏梭菌的混合富集培养物。 F. acidarmanus和Letotospirillum ferrooxidans dans。在整个实验过程中,通过拉曼光谱法监测矿物表面产物的化学形态变化。用扫描电子显微镜检查结构的演变,并将总可溶性铁用作溶出速率的量度。在所有三种矿物质的情况下,仅在存在铁氧化微生物(即酸曲霉或富集培养物)的情况下观察到溶解速率的增加。在相同条件下,存在这些铁氧化性物质时,矿物表面的化学形态与非生物控制反应的化学形态没有区别。两者均以元素硫为主。相比之下,用卡尔德斯酵母(T. caldus)进行的实验表明,矿物表面上元素硫的含量不到暴露于酸曲霉培养物样品上所观察到的含量的1%。令人惊讶的是,硫氧化物质从矿物表面除去元素硫也不会伴随矿物溶解速度的增加。这一发现表明,尽管元素硫在氧化溶解过程中在表面形成,但它不会钝化矿物表面。版权所有(C)2001 Elsevier Science Ltd. [参考:48]

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