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Microalgae shows a high potential to produce biofuel and forward osmosis (FO) has been proposed as a promising dewatering process for algal biomass separation from water. However, the effect of reverse salt flux (RSF) on algal biomass during the dewatering process using FO has not been completely explored. This study was to investigate the effect of different types of salt and their concentrations on algal biomass in terms of conductivity, settling velocity, and lipid contents in FS during a simulated FO-driven dewatering of Chlorella vulgaris microalgae. Three draw solution (DS) salts (NaCl, KCl and NH4Cl) were evaluated in RSF-simulating batch tests. The salt diffusion from the DS to the algal feed solution (FS) caused a static growth of algal biomass while increasing lipid content up to 14.8% at 8 mM NH4Cl. With the addition of the different salts, pH was maintained to the optimal algal thriving range (7.2–10.6), but the presence of salt stressed the algal cells and inhibited photosynthesis and algal growth within the experimental conditions. The settling velocity of the algal cells improved with the increase of salt content from 8 to 80 mM of each DS. It seemed that cell division could be accelerated in the presence of NH4Cl, and microscopic images showed a change in the algal cell size distribution, which may negatively affect algal settleability. DS salt in an FO-algal harvesting system should be selected based on the final algal properties and constituents required.

Trace minerals play an essential role in methane production via anaerobic digestion (AD). It is important to monitor Ni(II) and Co(II) concentrations and the Ni/Co concentration ratio for the rapid diagnosis of the ecological status or activity of methanogens in AD. Electrochemical detection of Ni(II) and Co(II) was investigated by coating the Bi-chitosan nanocomposite on a glassy carbon electrode (GCE) via the electrodeposition technique. A square-wave adsorptive cathodic stripping voltammetry technique (SWAdCSV) was applied and optimized when dimethylglyoxime (DMG) was used as the chelating agent for Ni(II) and Co(II) measurements. The SWAdCSV results showed that the current peaks for Co(II) detection are 6.1 times greater than the current peaks for Ni(II) measurements, probably due to the different affinity of DMG molecules between Ni(II) and Co(II). DMG molecules demonstrated higher selectivity toward Co(II) cations compared to Ni(II). The modified Bi-chitosan GCE developed in this study showed a relatively wide range of the Ni(II) and Co(II) concentrations (2–100 µg L−1) with a limit of detection of 3.6 µg L−1 for Ni(II) and 2.4 µg L−1 for Co(II), respectively. The developed sensor was applied to Ni(II) and Co(II) spiked natural water samples and showed good performance of detection with 12 consecutive measurements. Overall, the fabricated sensor showed excellent sensitivity toward Ni(II) and Co(II) in natural water samples.

Per- and poly-fluoroalkyl substances (PFASs) have recently been labeled as toxic constituents that exist in many aqueous environments. However, traditional methods used to determine the level of PFASs are often not appropriate for continuous environmental monitoring and management. Based on the current state of research, PFAS-detecting sensors have surfaced as a promising method of determination. These sensors are an innovative solution with characteristics that allow for in situ, low-cost, and easy-to-use capabilities. This paper presents a comprehensive review of the recent developments in PFAS-detecting sensors, and why the literature on determination methods has shifted in this direction compared to the traditional methods used. PFAS-detecting sensors discussed herein are primarily categorized in terms of the detection mechanism used. The topics covered also include the current limitations, as well as insight on the future direction of PFAS analyses. This paper is expected to be useful for the smart sensing technology development of PFAS detection methods and the associated environmental management best practices in smart cities of the future.