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Extracellular Polymeric Substances from Bacillus subtilis Associated with Minerals Modify the Extent and Rate of Heavy Metal Sorption

机译:枯草芽孢杆菌与矿物质相关的细胞外聚合物改变了重金属吸附的程度和速率

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摘要

Extracellular polymeric substances (EPS) are an important source of organic matter in soil. Once released by microorganisms, a portion may be sorbed to mineral surfaces, thereby altering the minerals ability to immobilize heavy metals. EPS from Bacillus subtilis were reacted with Ca-saturated bentonite and ferrihydrite in 0.01 M KCI at pH 5.0 to follow the preferential uptake of EPS-C, -N, and -P. The sorption kinetics of Pb~(2+), Cu~(2+), and Zn~(2+) to the resulting EPS-mineral composites was studied in single and binary metal batch experiments ([metal]_(totoal) = 50μM, pH 5.0). Bentonite sorbed much more EPS-C (18.5 mg g~(-1)) than ferrihydrite (7.9 mg g~(-1)). During sorption, EPS were chemically and size fractionated with bentonite favoring the uptake of low-molecular weight components and EPS-N, and ferrihydrite selectively retaining high-molecular weight and P-rich components. Surface area and pore size measurements by N_2 gas adsorption at 77 K indicated that EPS altered the structure of mineral-EPS associations by inducing partial disaggregation of bentonite and aggregation of ferrihydrite. Whereas mineral-bound EPS increased the extent and rate of Pb~(2+), Cu~(2+), and Zn~(2+) sorption for bentonite, either no effect or a decrease in metal uptake was observed for ferrihydrite. The extent of sorption always followed the order Pb~(2+) > Cu~(2+) > Zn~(2+), which also prevailed in binary Pb~(2+)/Cu~(2+) systems. In consequence, sorption of EPS to different minerals may have contrasting consequences for the immobilization of heavy metals in natural environments by inducing mineral-specific alterations of the pore size distribution and, thus, of available sorption sites.
机译:细胞外聚合物(EPS)是土壤中有机物的重要来源。一旦被微生物释放,一部分可能会吸附到矿物表面,从而改变矿物固定重金属的能力。将枯草芽孢杆菌的EPS与Ca饱和膨润土和水铁矿在0.01 M KCl中于pH 5.0下反应,以优先吸收EPS-C,-N和-P。在单批和双批金属分批实验中研究了Pb〜(2 +),Cu〜(2+)和Zn〜(2+)对所得EPS矿物复合材料的吸附动力学([metal] _(totoal)= 50μM,pH 5.0)。膨润土吸收的EPS-C(18.5 mg g〜(-1))比三水铁酸盐(7.9 mg g〜(-1))高得多。在吸附过程中,EPS用膨润土进行化学分离和粒度分级,有利于吸收低分子量组分和EPS-N,三水铁矿则选择性地保留了高分子量和富含P的组分。在77 K下通过N_2气体吸附进行的表面积和孔径测量表明,EPS通过引起膨润土的部分解聚和水铁矿的聚集而改变了矿物-EPS的缔合结构。矿物结合的EPS增加了膨润土对Pb〜(2 +),Cu〜(2+)和Zn〜(2+)的吸附程度和吸附速率,而对三水铝石则没有影响,也没有观察到金属吸收的减少。吸附程度始终遵循Pb〜(2+)> Cu〜(2+)> Zn〜(2+)的顺序,在二元Pb〜(2 +)/ Cu〜(2+)系统中也很普遍。因此,EPS诱导不同矿物质的吸附可能会导致自然环境中重金属的固定化,从而引起孔径分布的矿物质特异性变化,进而导致可用的吸附位点发生变化。

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  • 来源
    《Environmental Science & Technology》 |2012年第7期|p.3866-3873|共8页
  • 作者单位

    Institut fur Bodenkunde, Leibniz Universitat Hannover, Germany;

    Institut fur Bodenkunde, Leibniz Universitat Hannover, Germany;

    Federal Institute for Geosdences and Natural Resources (BGR), Hannover, Germany;

    Department of Soil Ecology, Bayreuth Center of Ecology and Environmental Research (BayCEER), University of Bayreuth,Germany;

    Institut fur Bodenkunde, Leibniz Universitat Hannover, Germany;

  • 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);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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