Adsorption of Cr(VI) and Cr(III) on layered pipe scales and the effects of disinfectants in drinking water distribution systems.

Pipe scales in drinking water distribution systems (DWDS) potentially adsorb chromium (Cr). Meanwhile, the fate of Cr in pipe scales and water could be influenced by the disinfectants used in DWDS since they might influence the valence state of Cr. Therefore, the adsorption of Cr (Cr(VI) and Cr(III)) on pipe scales, the transformation between different valence states, and the effects of disinfectants present in DWDS are important research topics for improving tap water quality but have not yet been sufficiently investigated. This study investigated the properties of layered pipe scales and conducted adsorption kinetic experiments in single and binary Cr(VI) and Cr(III) systems, as well as experiments related to the oxidation and adsorption of Cr(III) under the influence of decaying disinfectants. According to the results, pipe scales exhibited distinct layered structures with varying mechanisms for the adsorption of Cr(VI) and Cr(III). Cr(VI) was adsorbed through surface complexation on the surface and porous core layers, while redox reactions predominantly occurred on the shell-like layer. Furthermore, Cr(III) was adsorbed via surface precipitation on the three-layer pipe scales. Importantly, disinfectants promoted the transformation of Cr(III) to the less readily released Cr(VI) in pipe scales, reducing the Cr exposure risk from the pipe scale phase. Pipe scales also decreased the Cr(VI) concentration in water (almost 0 mg/L), enhancing the safety of DWDS. This study provides theoretical guidance on the safe operation of DWDS.

Cu fate driven by colloidal polystyrene microplastics with pipe scale destabilization in drinking water distribution systems.

Microplastics (MPs) and Cu have been detected in drinking water distribution systems (DWDSs). Investigating MP effects on Cu adsorption by pipe scales and concomitant variations of pipe scales was critical for improving the water quality, which remained unclear to date. Therefore, polystyrene microplastics (PSMPs) were adopted for the model MPs to determine their effects on Cu fate and pipe scale stabilization, containing batch adsorption, metal speciation extraction, and Cu release experiments. Findings demonstrated that complexation and electrostatic interactions were involved in Cu adsorption on pipe scales. PSMPs contributed to Cu adsorption via increasing negative charges of pipe scales and providing additional adsorption sites for Cu, which included the carrying and component effects of free and adsorbed PSMPs, respectively. The decreased iron and manganese oxides fraction (45.57 % to 29.91 %) and increased organic fraction (48.51 % to 63.58 %) of Cu in pipe scales when PSMPs were coexisting illustrated that PSMPs had a greater affinity for Cu than pipe scales and thus influenced its mobility. Additionally, the release of Cu could be facilitated by the coexisted PSMPs, with the destabilization of pipe scales. This study was the first to exhibit that Cu fate and pipe scale stabilization were impacted by MPs, providing new insight into MP hazards in DWDSs.

The effect of adsorption on the fate of colloidal polystyrene microplastics in drinking water distribution system pipe scales.

With microplastics (MPs) being continuously found in various environments, the pollution of water supply systems by MPs is receiving increasing attention. As the sediment in drinking water distribution systems (DWDSs), pipe scales act as the interface for complex reactions between bulk water and pipe surfaces. Consequently, the fate of MPs in pipe scales requires exploration, especially colloidal MPs. In this study, MPs were detected in different pipe scale layers, with concentrations of 0.32-3.10 items g-1. Subsequently, the adsorption interaction mechanisms between pipe scales and colloidal polystyrene microplastics (PSMPs) were investigated through batch adsorption experiments. The findings indicated that pipe scales showed a potential adsorption capacity for PSMPs. The adsorption kinetics and isotherms results demonstrated that the PSMP adsorption process was physically dominant and complicated. van der Waals and electrostatic interactions, hydrogen bonding, and pore filling were the main adsorption mechanisms. These results verify that colloidal MPs can be adsorbed by pipe scales, demonstrating that pipe scales play an essential role in the fate of colloidal MPs in DWDSs and the quality and security of drinking water. The secondary release of MPs from pipe scales is also worthy of attention due to the environmental and health risks.

Important Role of Concave Surfaces in Deposition of Colloids under Favorable Conditions as Revealed by Microscale Visualization.

This study conducted saturated column experiments to systematically investigate deposition of 1 µm positively charged polystyrene latex micro-colloids (representing microplastic particles) on negatively charged rough sand, glass beads, and soil with pore water velocities (PWV) from 4.9 × 10-5 to 8.8 × 10-4 m/s. A critical value of PWV was found below which colloidal attachment efficiency (AE) increased with increasing PWV. The increase in AE with PWV was attributed to enhanced delivery of the colloids and subsequent attachment at concave locations of rough collector surfaces. The AE decreased with further increasing PWV beyond the threshold because the convex sites became unavailable for colloid attachment. By simulating the rough surfaces using the Weierstrass-Mandelbrot equation, the extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) interaction energy calculations and torque analysis revealed that the adhesive torques could be reduced to be comparable or smaller than hydrodynamic torques even under the favorable conditions. Interestingly, scanning electron microscopic experiments showed that blocking occurred at convex sites at all ionic strengths (ISs) (e.g., even when the colloid-colloid interaction was attractive), whereas at concave sites, blocking and ripening (i.e., attached colloids favor subsequent attachment) occurred at low and high ISs, respectively. To our knowledge, our work was the first to show coexistence of blocking and ripening at high ISs due to variation of the collector surface morphology.

Occurrence and distribution of microplastics in water supply systems: In water and pipe scales.

Microplastic (MP) pollution has received widespread attention; however, its occurrence and distribution in water supply systems, particularly in pipe scales, remains unclear. In this study, MPs were observed in water and pipe scale samples from the drinking water treatment plant (DWTP) and distribution system (DWDS), respectively. The MP concentrations ranged from 13.23 to 134.79 n/L and 569.99 to 751.73 n/kg in the water and pipe scale samples, respectively. The predominant particles in the pipe scales (50-100 µm) were smaller than those in the water samples (> 200 µm). Overall, MP fragments were the most abundant. Of all the identified MPs, nylon and polyvinyl chloride were predominant in the water and pipe scale samples, respectively. Furthermore, the DWTP and DWDS both prevented MPs from entering the tap water, thereby reducing their risk. The results of this study provide direct evidence for the strong adsorption of MPs onto pipe scales, indicating that pipe scale stability may play a role in improving water quality and security. However, the abundance of MPs in pipe scales cannot be ignored. Additionally, the results provide valuable background information on MP pollution in water supply systems.

Field study on the characteristics of scales in damaged multi-material water supply pipelines: Insights into heavy metal and biological stability.

Microbial corrosion and heavy metal accumulation in metal water supply pipelines aggravate scale formation and may result in pipeline leakage or bursting events. To better understand the corrosion and corrosion products in the damaged pipes, deposits excavated from three damaged pipes after 22-26 year service periods were analyzed. Using a combination of advanced micro-mineral techniques and 16S rRNA high-throughput sequencing, the micromorphology, chemical composition, and bacterial community were investigated systematically. Unlined pipe wall scales ruptured while lined pipes leaked due to joint scales. Dendrogram correlation results demonstrated that V/As, Al/Pb, and Cr/Mn clusters exhibited co-adsorption and co-precipitation characteristics. FTIR and XRD analysis detected the presence of γ-FeOOH, α-FeOOH in loose scales, and Fe3O4 in rigid scales. Scales were colonized by various corrosion bacteria, with sulfate reducing bacteria and ammonia producing bacteria being dominant in the scales of anticorrosive and non-corrosive pipe, respectively. Tl, Ca, Al, and Pb exhibited an extremely positive correlation with Rhodocyclaceae, Ferritrophicum, Thermodesulfovibrionia, and Clostridiaceae. Al and V presented a potential Hazard Quotient risk to consumers, while Cd was potentially bioavailable in all inner scales. Overall, this study provides valuable information for the effective management and avoidance of corrosion-induced pipeline damage and heavy metal release.