Zhuang Jie, Jin Yan
Department of Plant and Soil Sciences, University of Delaware, Newark, DE 19717-1303, USA.
J Contam Hydrol. 2003 Feb;60(3-4):193-209. doi: 10.1016/s0169-7722(02)00087-6.
Knowledge of the factors that influence the fate and transport of viruses in porous media is very important for accurately determining groundwater vulnerability and for developing protective regulations. In this study, six saturated sand column experiments were performed to examine the effects of a positively charged Al-oxide, which was coated on sand particles, on the retention and transport of viruses (phiX174 and MS-2) in background solutions of different ionic strength and composition. We found that the Al-oxide coating on sand significantly removed viruses during their transport in a phosphate buffered saline (PBS) solution. Mass balance calculations showed that 34% of the input MS-2 was inactivated/irreversibly sorbed on the surface of Al-oxide coated sand whereas 100% of phiX174 was recovered. Results from this study also indicated that higher ionic strength facilitated the transport of both phiX174 and MS-2 through the Al-oxide coated sand. This was attributed to the effect of ion shielding, which at higher ionic strength decreased the electrostatic attraction between the viral particles and the sand surface and consequently decreased virus sorption. Strong effect of the ionic strength indicates that an outer-sphere complexation mechanism was responsible for the virus sorption on the Al-oxide coated sand. Ion composition of the background solutions was also found to be a significant factor in influencing virus retention and transport. Virus transport was enhanced in the presence of phosphate (HPO(4)(2-)) as compared to bicarbonate (HCO(3)(-)), and the effect of HPO(4)(2-) was more significant on MS-2 than on phiX174. The presence of bivalent cations (Ca(2+) and Mg(2+)) increased virus transport because the cations partially screened the negative charges on the viruses therefore decreased the electrostatic attraction between the positively charged sand surface and the negatively charged viruses. Mass recovery data indicated that bivalent cations gave rise to a certain degree of inactivation/irreversibly sorption of phiX174 on the surface of Al-oxide coated sand. On the contrary, the bivalent cations appeared to have protected MS-2 from inactivation/irreversibly sorption. This study provides some insights into the mechanisms responsible for virus retention and transport in porous media.
了解影响病毒在多孔介质中归宿和运移的因素,对于准确确定地下水脆弱性和制定保护法规非常重要。在本研究中,进行了六个饱和砂柱实验,以研究包覆在砂粒上的带正电荷的氧化铝对不同离子强度和组成的背景溶液中病毒(φX174和MS-2)的截留和运移的影响。我们发现,砂上的氧化铝涂层在病毒于磷酸盐缓冲盐水(PBS)溶液中运移期间显著去除了病毒。质量平衡计算表明,输入的MS-2中有34%在包覆氧化铝的砂表面失活/不可逆吸附,而φX174的回收率为100%。本研究结果还表明,较高的离子强度促进了φX174和MS-2通过包覆氧化铝的砂的运移。这归因于离子屏蔽效应,在较高离子强度下,离子屏蔽效应降低了病毒颗粒与砂表面之间的静电吸引力,从而减少了病毒吸附。离子强度的强烈影响表明,外层络合机制是病毒在包覆氧化铝的砂上吸附的原因。还发现背景溶液的离子组成是影响病毒截留和运移的一个重要因素。与碳酸氢根(HCO₃⁻)相比,磷酸盐(HPO₄²⁻)存在时病毒运移增强,且HPO₄²⁻对MS-2的影响比对φX174更显著。二价阳离子(Ca²⁺和Mg²⁺)的存在增加了病毒运移,因为阳离子部分屏蔽了病毒上的负电荷,因此降低了带正电荷的砂表面与带负电荷的病毒之间的静电吸引力。质量回收数据表明,二价阳离子导致φX174在包覆氧化铝的砂表面有一定程度的失活/不可逆吸附。相反,二价阳离子似乎保护了MS-2不被失活/不可逆吸附。本研究为多孔介质中病毒截留和运移的机制提供了一些见解。