A novel understanding of residual nano-Al13 formation and degradation during coagulation and flocculation: a proof based on ESI-TOF-MS

Abstract

Nano-Al₁₃ clusters have the potential to form and remain in a coagulation process, but cannot be directly traced by traditional instrumental techniques in real time since there is only a trace concentration after being dosed. In this study, an optimized electrospray ionization mass spectrometry (ESI-MS) method was introduced for the first time to determine the coagulation pathways when using AlCl₃ (monomeric Al, i.e., Al_m) and polymeric aluminum chloride (PACl) as coagulants. The transformation mechanisms of Al clusters, including Al_m, oligomeric Al (Al_o), Al₁₃ and transient Al (Al_ts), were clearly elucidated using statistical analysis and a real-time tracking experiment. The nano-Al₁₃ clusters could be detected in the coagulation batch experiment conducted using AlCl₃ as the coagulant. Moreover, using a statistical method, the Al₁₃ clusters in the PACl coagulant and the Al₁₃ clusters formed by AlCl₃ coagulation were confirmed to be an efficient coagulant species. In the real-time tracking experiments, the reversible transformations among Al_m, Al_o, Al₁₃ and Al_ts clusters were instantly observed after the addition of the coagulant (i.e., during the coagulation process). In the subsequent process (i.e., the flocculation process), only floc aggregation occurred, and no obvious transformations among the four types of Al clusters were observed. The continuous aggregation and increase in floc were mainly attributed to particle coalescence with the Al clusters. The mineral–water interface was inferred to favor the transformation of Al_m and Al_o aggregates into Al₁₃ as well as the reverse reaction (e.g., the degradation of Al₁₃).