Virus adsorption to colloidal particles is an important issue in the water quality community. Namely, if viruses can quickly and strongly associate to colloids, this can potentially lead to significant implications for the management of biohazardous wastes at water reclamation facilities. This research evaluated the adsorption of bacteriophage MS2 to colloidal suspensions of kaolinite (KAO) and fiberglass (FG). Observed pseudo first-order MS2 removal rate constants were between 0.53 and 5.1 min-1 and between 2.4 and 3.5 min-1 for KAO and FG, respectively. These kinetics were at least an order of magnitude faster than previously reported values when compared to data retrieved at similar colloid concentrations. Fluorescent and bright field microscopic images showed clusters of MS2 on and around the edges of the colloids, and the majority of the bound MS2 was not readily removed during a vigorous wash step, suggesting comparatively strong, operationally relevant adsorption. MS2 aggregation was observed experimentally and predicted on the basis of interaction energies calculated with XDLVO models. When virus-containing biohazardous wastes are introduced into wastewater treatment plants, removing colloids is essential.

Forward osmosis (FO) technology has a broad application prospect in the field of liquid food concentration because of the complete retention of flavor components and bioactive substances. Membrane fouling is the main obstacle affecting the FO performance and concentration efficiency. This work systematically investigated the membrane fouling behavior of the FO process for fruit juice concentration elucidated by the models of resistance-in-series, xDLVO theory and FTIR analysis. The results show that the AL-FS mode was more suitable for concentrating orange juice. Increasing the cross-flow rate and pretreatment of feed solutions can effectively improve the water flux and reduce the fouling resistance. The ATR-FTIR analysis revealed that the fouling layer of orange juice was mainly composed of proteins and polysaccharides, and the pretreatment of microfiltration can greatly reduce the content of the major foulant. There was an attractive interaction between the FO membrane and orange juice foulants; by eliminating those foulants, the microfiltration pretreatment then weakened such an attractive interaction and effectively prevented the fouling layer from growing, leading to a lower process resistance and, finally, resulting in a great improvement of concentration efficiency.

The transport behaviors of nanomaterials, in especial multifunctional nanohybrids have not been well disclosed until now. In this study, environmentally relevant conditions, including cation types, ionic strength and pH, were selected to investigate the transport and retention of graphene oxide-hematite (GO-Fe2O3) nanohybrids and a photoaged product in saturated sandy columns. Results show that more hybridization of hematite led to decreased negative surface charge, while increased particle size and hydrophobicity of the nanohybrids, which depressed their transport according to extented Derjaguin-Landau-Verwey-Overbeek (XDLVO) theory. However, the inhibitory transport of photoaged nanohybrids was attributed to their distinct surface roughness caused by relatively high hybridization and photoirradiation. Notably the restrained transport was alleviated in the CaCl2 saturated media, since the less surface O-functional groups of the corresponding nanohybrids reduced the cation bridging effect caused by Ca2+. Similarly, increasing pH promoted the transport of the nanohybrids in NaCl saturated media, particularly for the nanohybrids that contained rich O-functional groups, but exerted inconspicuous effect on mobility of the nanohybrids in CaCl2 saturated media. These observations highlight that both XDLVO interactions and surface roughness may work together to impact the transport and fate of the burgeoning, versatile nanohybrids in the environment.

Attachment of human adenovirus 40 (HAdV40) onto surfaces coated with three compositionally different household paints was evaluated experimentally and interpreted based on measured physicochemical properties of the paints. Polar, dispersive and electrostatic interactions between HAdV40 and the paints were predicted using the extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) model. Quartz crystal microbalance (QCM-D) was used to quantify virus attachment to paints from 1 mM and 150 mM NaCl solutions, with the latter having the ionic strength of a typical respiratory fluid. Acrylic latex water-based, alkyd water-based, and alkyd oil-based paints were all determined to be highly hydrophobic (ΔGsws < - 48 mJ/m2). XDLVO modeling and preliminary QCM-D tests evaluated virus-paint interactions within and outside pH windows of favorable virus-paint electrostatic interactions. Hydrophobic and electrostatic interactions governed virus attachment while van der Waals interactions played a relatively minor role. In higher ionic strength solutions, the extent of virus attachment correlated with the free energy of virus-paint interfacial interaction, [Formula: see text] : more negative energies corresponded to higher values of the areal mass density of attached viruses. Hydrophobicity was the dominant factor in determining virus adhesion from high ionic strength solutions where electrostatic interactions were screened out. The hydrophobicity of paints, while desirable for minimizing moisture intrusion, also facilitates attachment of colloids such as viruses. The results call for new approaches to the materials design of indoor paints with enhanced resistance to virus adhesion. Paints so formulated should help reduce human exposure to viruses.

Membranes have a lot of potential for harvesting microalgae, but membrane fouling is hampering their breakthrough. In this study, the effects of charge and corrugated surface on membrane filtration performance were investigated. The clean water permeance (CWP), the microalgae harvesting efficiency and the membrane flux for a microalgal broth were determined using patterned polysulfone (PSf) membranes with different shapes of the surface patterns and containing different charge densities by blending sulfonated polysulfone (sPSf). The flow behavior near the patterned membrane surface, as well as the interaction energy between membrane and microalgae were investigated using computational fluid dynamics (CFD) simulation and the improved extended \"Derjaguin, Landau, Verwey, Overbeek\" (XDLVO) theory, respectively. Membrane charge and pattern shape significantly improve the membrane performance. The critical pressures of all sPSf blend patterned membranes were higher than 2.5 bar. A 4.5w% sPSf blend patterned membranes with wave patterns showed the highest CWP (2300 L/m2 h bar) and membrane flux in the microalgal broth (1000 L/m2 h bar) with 100% harvesting efficiency. XDLVO analysis showed that sPSf blend patterned membranes prepared obtained the lowest interaction energy and highest energy barrier for microalgal attachment. CFD simulation showed a higher velocity and wall shear on the pattern apexes.

Biofouling is a key problem in membrane filtration, and extracellular polymer substances (EPS) play a key role in biofouling. Biofouling contributes to membrane fouling during ultrafiltration of up-flow biological activated carbon filter (UBACF) effluent. EPS are released when pollutants get attached with membrane surface and when pollutants are in solution phase from cell lysis and by cell secretions. In our study of EPS + humic acid (HA) prepared as the effluent pollutants for ultrafiltration, we found that EPS increased the interfacial forces between the pollutants and the membrane, resulting in membrane fouling. In the early stages of filtration, the main contribution of EPS to membrane fouling was to bond with organic colloids, which led to an increase in the pollutant particle size and zeta potential. This increased the short-range Lewis acid-base (AB) forces from -4.89 nN to -12.59 nN and accelerated the formation of a cake layer. In the late stage of filtration, the EPS increased both the AB and London-van der Waals (LW) forces, thus accelerating membrane fouling. In order to mitigate biofouling, we developed a method of pretreating the effluent with 0.4 mg/L ozone prior to ultrafiltration and backwashing with 8 mg/L H2O2 to sterilize bacteria attached to the membrane surface. This method not only changed the characteristics of the EPS, but also inactivated bacteria by disinfection with H2O2, thereby reducing the amount of EPS. The proposed method provided a long-term stable operation guarantee for ultrafiltration of UBACF effluent.

OBJECTIVE: Drying-induced decrease in lip balm surface energy enhances virus adhesion due to the emergence of strong hydrophobic colloid-surface interactions.
METHODS: A protocol was developed for preparing lip balm coatings to enable physicochemical characterization and adhesion studies. Surface charge and hydrophobicity of four brands of lip balm (dry and hydrated) and human adenovirus 5 (HAdV5) were measured and used to calculate the extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) energy of interactions between lip balm coatings and HAdV5 as well as four other colloids: HAdV40, MS2 and P22 bacteriophages, and SiO2. Quartz crystal microbalance with dissipation monitoring (QCM-D) tests employed SiO2 colloids, HAdV5 and hydrated lip balms.
RESULTS: Drying of lip balms results in a dramatic decrease of their surface energy (δΔGsws≥ 83.0 mJ/m2) making the surfaces highly hydrophobic. For dry lip balms, the interaction of the balm surface with all five colloids is attractive. For lip balms hydrated in 150 mM NaCl (ionic strength of human saliva), XDLVO calculations predict that hydrophilic colloids (MS2, P22, SiO2) may attach into shallow secondary minima. Due to the relative hydrophobicity of human adenoviruses, primary maxima in XDLVO profiles are low or non-existent making irreversible deposition into primary energy minima possible. Preliminary QCM-D tests with SiO2 colloids and HAdV5 confirm deposition on hydrated lip balms.

To understand the biofilm formation of biofilm-based processes in wastewater treatment plants (WWTPs), the interaction mechanisms between extracted extracellular polymeric substances (EPS) and three model carrier surfaces (i.e., negatively charged hydrophilic silica, positively charged hydrophilic alumina, and neutral charged hydrophobic polystyrene) were investigated employing a laboratory quartz crystal microbalance with dissipation monitoring equipment (QCM-D) and an atomic force microscope (AFM). The data suggested that surface charge and hydrophobicity of both EPS and carriers played significant roles in the interaction behaviors. Moreover, increases in ionic strength could lead to the increasing zeta potential and hydrophobicity of EPS. It is worth noting that long-range DLVO forces dominated the EPS deposition on carriers in lower ionic strength while short-range Lewis acid-base (AB) interaction controlled the adhesion behaviors in higher ionic strength. Besides, the presence of calcium ions contributed to the adhesion behaviors because of strong charge neutralization and hydrophobic effect. Bound EPS (BEPS) showed higher affinity to model carriers than dissolved EPS (DEPS), which conformed to XDLVO prediction rather than classical DLVO model. Overall, these results provide insights into the influence mechanisms of carrier characteristics, ionic strength, calcium ion and EPS components on the interaction between EPS and representative carriers, contributing to predict and regulate biofilm formation in biofilm-based processes.

This work systematically studied the role of pre-coagulation in the performance of ultralow pressure membrane system for algae-laden water treatment. The membrane performance with/without pre-coagulation was compared in terms of membrane permeate flux, water quality and membrane fouling. Ultralow pressure membrane system can effectively reduce TOC of Microcystis aeruginosa-laden water from 5.8 to 2.1 mg/L, and pre-coagulation removed most large inorganic particles but few small organic particles. Interestingly, pre-coagulation aggravated the fouling of ultralow membrane system which is generally acknowledged method to alleviate the ultrafiltration membrane fouling. According to Extended Derjaguin-Landau-Verwey-Overbeek theory (XDLVO), the interaction energy of membrane-foulants (ΔGfmTOT = - 41.95mJ/m2), and foulant-foulant (ΔGffTOT = - 30.15mJ/m2) with coagulation were higher than those without coagulation (ΔGfmTOT = - 36.54mJ/m2) and (ΔGffTOT = - 15.73mJ/m2) suggesting greater adherence between membrane and foulants & foulant and foulant after coagulation, which well agreed with SEM results. Membrane fouling models were also applied to analyze the fouling mechanism of ultralow-pressure membrane filtration. Based on above analysis, the possible fouling mechanisms for membrane filtration with/without precoagulation were proposed and then confirmed by pre-filtration experiment, where large inorganic particles played important roles. Our study could be indicative for membrane fouling control of ultralow-pressure membrane filtration for the treatment of algae-laden water.

Although nanoscale surface roughness has been theoretically demonstrated to be a crucial factor in the interaction of colloids and surfaces, little experimental research has investigated the influence of roughness on colloid or silver nanoparticle (AgNP) retention and release in porous media. This study experimentally examined AgNP retention and release using two sands with very different surface roughness properties over a range of solution pH and/or ionic strength (IS). AgNP transport was greatly enhanced on the relatively smooth sand in comparison to the rougher sand, at higher pH, and lower IS and fitted model parameters showed systematic changes with these physicochemical factors. Complete release of the retained AgNPs was observed from the relatively smooth sand when the solution IS was decreased from 40 mM NaCl to deionized (DI) water and then the solution pH was increased from 6.5 to 10. Conversely, less than 40% of the retained AgNPs was released in similar processes from the rougher sand. These observations were explained by differences in the surface roughness of the two sands which altered the energy barrier height and the depth of the primary minimum with solution chemistry. Limited numbers of AgNPs apparently interacted in reversible, shallow primary minima on the smoother sand, which is consistent with the predicted influence of a small roughness fraction (e.g., pillar) on interaction energies. Conversely, larger numbers of AgNPs interacted in deeper primary minima on the rougher sand, which is consistent with the predicted influence at concave locations. These findings highlight the importance of surface roughness and indicate that variations in sand surface roughness can greatly change the sensitivity of nanoparticle transport to physicochemical factors such as IS and pH due to the alteration of interaction energy and thus can strongly influence nanoparticle mobility in the environment.