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Monitoring lithium ions (Li+) in lithium-rich brine (LrB) is critical for metal recovery, yet challenges such as high ionic strength and gypsum-induced surface deterioration hinder the performance of potentiometric ion-selective electrode (ISE) sensors. This study advances the functionality of Li+ ISE sensors and enables continuous monitoring of Li+ concentration in LrB by introducing apolyelectrolyte multilayer (PEM) of poly(allylamine hydrochloride)/poly(sodium 4-styrenesulfonate) (PAH/PSS) that serves as an antigypsum scaling material to minimize nucleation on the sensor surface. With 5.5 bilayers of PAH/PSS coating, the Li+ ISE sensors possess a high Nernst slope (59.14 mV/dec), rapid response (+, log Ks = -2.35; K+, log Ks = -2.47; Ca2+, log Ks = -4.05; Mg2+, log Ks = -4.18). The impedance (85.1 kΩ) of (PAH/PSS)5.5-coated sensors is 1 order of magnitude lower than that of electrospray ion-selective membrane (E-ISM) Li+ sensors (830 kΩ), attributed to the ultrathin (45.3 nm) and highly dielectric PAH/PSS bilayers. During a 15-day continuous monitoring test in LrB, the (PAH/PSS)5.5-coated Li+ ISE sensors with their superhydrophilic and smooth surface diminish nucleation sites for scaling agents (e.g., Ca2+ and SO42-) and consequently mitigate gypsum scaling. Moreover, a brine-tailored denoising data processing algorithm (bt-DDPA), coupled with the salinity-adjusted mathematical model with Lagrange interpolation, effectively captures Li+ fluctuation by filtering out anomalies and reducing sensor drift in brine. Bt-DDPA alleviates the discrepancy between the sensor readings and the lab-based validation results by 46.06%. This study demonstrates that the integration of material advancement (PAH/PSS coating) with sensor data processing (bt-DDPA) bolsters continuous and accurate Li+ monitoring in LrB, crucial for brine water treatment and resource recovery.
Xiang et al. (Tue,) studied this question.