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Effect of dissolved organic matter on the stability of magnetite nanoparticles under different pH and ionic strength conditions

机译:不同pH和离子强度条件下溶解有机物对磁铁矿纳米颗粒稳定性的影响

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摘要

Upon release of engineered nanoparticles (NPs) into the subsurface environment, their fate and transport and hence their potential environmental and public health impacts will largely depend on how stable these NPs are as suspended particles in the natural environment. In this study, we systematically examine the effect of humic acid (HA) on surface charge status and aggregation potential of magnetite (Fe_3O_4) NPs, selected as a model for metal oxide NPs, over a wide range of solution pH and ionic strength. Through zeta potential (ZP) measurements, we found that HA can adsorb to magnetite particles hence modifying their surface charge status. At low loadings, the presence of HA can induce a shift in the point zero of charge of due to partial neutralization of the positive charges on magnetite NPs. At high loadings, however, HA is capable of completely cover magnetite particles giving rise to a suspension ZP profile similar to its own (observed in presence of 20 mg L~(-1) HA). These impacts on surface charge correspond well with the observed aggregation behaviors in the absence and presence of HA. From the dynamic light scattering (DLS) measurements, fast aggregation, which is independent of solution chemistry, took place when the pH is close to the point zero charge (PZC) and the ionic strength is above the critical coagulation concentration (CCC). At high ionic strength, a small dose (2 mg L~(-1)) of HA stabilized the NPs' suspension significantly. This stabilization effect is substantially enhanced with increasing HA concentration. The calculated DLVO (Derjaguin-Landau-Verwey-Overbeek) interaction energy profiles, using experimentally determined values of Hamaker constant, adequately support the experimental observations. The DLVO analysis further reveals the possible presence of secondary energy minima and the possibility of deaggregation of magnetite agglomerates. The complexation of HA-NPs and the HA effects on NPs aggregations were confirmed by atomic force microscope (AFM) observations.
机译:在将工程纳米颗粒(NPs)释放到地下环境中时,它们的命运和运输以及因此对环境和公共健康的潜在影响将在很大程度上取决于这些NPs作为悬浮颗粒在自然环境中的稳定性。在这项研究中,我们系统地研究了腐殖酸(HA)对被选作金属氧化物NPs模型的磁铁矿(Fe_3O_4)NPs在广泛的溶液pH和离子强度范围内的表面电荷状态和聚集势的影响。通过zeta电位(ZP)测量,我们发现HA可以吸附到磁铁矿颗粒上,从而改变其表面电荷状态。在低负荷下,由于磁铁矿NPs上正电荷的部分中和,HA的存在会引起零电荷点的偏移。但是,在高负荷下,HA能够完全覆盖磁铁矿颗粒,从而产生类似于其自身的悬浮ZP曲线(在20 mg L〜(-1)HA存在下观察到)。这些对表面电荷的影响与在不存在和存在HA的情况下观察到的聚集行为非常吻合。根据动态光散射(DLS)测量,当pH值接近零电荷点(PZC)且离子强度高于临界凝结浓度(CCC)时,发生了与溶液化学无关的快速聚集。在高离子强度下,小剂量(2 mg L〜(-1))的HA可显着稳定NPs的悬浮液。随着HA浓度的增加,这种稳定作用会大大增强。使用实验确定的Hamaker常数值计算得出的DLVO(Derjaguin-Landau-Verwey-Overbeek)相互作用能谱,充分支持了实验观察。 DLVO分析进一步揭示了次级能量极小值的存在和磁铁矿团块解聚的可能性。 HA-NPs的复合以及HA对NPs聚集的影响已通过原子力显微镜(AFM)的观察得到证实。

著录项

  • 来源
    《Science of the total environment》 |2010年第16期|P.3477-3489|共13页
  • 作者单位

    Laboratory for Earth Surface Processes (LASP), College of Urban and Environmental Sciences. Peking University. Beijing, 100871, China;

    rnEnvironmental Soil Physics Lab, Department of Plant and Soil Sciences, University of Delaware, Newark, Delaware, 19716, USA;

    rnElectromagnetic Materials Laboratory, Department of Physics and Astronomy, University of Delaware. Newark, Delaware, 19716, USA;

    rnElectromagnetic Materials Laboratory, Department of Physics and Astronomy, University of Delaware. Newark, Delaware, 19716, USA;

    rnLaboratory for Earth Surface Processes (LASP), College of Urban and Environmental Sciences. Peking University. Beijing, 100871, China;

    rnEnvironmental Soil Physics Lab, Department of Plant and Soil Sciences, University of Delaware, Newark, Delaware, 19716, USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    engineered nanoparticle; magnetite; aggregation; stability kinetics; humic acid; DLVO theory; AFM;

    机译:工程纳米颗粒;磁铁矿;聚合;稳定性动力学;腐植酸;DLVO理论;原子力显微镜;
  • 入库时间 2022-08-17 13:56:15

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