pH-Regulated microelectrolysis-kaolinite coupling for Heterosigma akashiwo removal
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Updated: Nov 4, 2026

Electrochemically and Bioelectrochemically Induced Ammonium Recovery
Published on: January 22, 2015
Zelong Wei1, Zhiming Yu1, Xiaomiao Zang1
1Laboratory of Marine Ecology and Environmental Sciences, Shandong Province Key Laboratory of Marine Biodiversity and Bio-resource Sustainable Utilization, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China; University of Chinese Academy of Sciences, Beijing, 100049, China; Laboratory for Marine Ecology and Environmental Science, Qingdao Marine Science and Technology Center, Qingdao, 266237, China.
Abstract:
Mineral-assisted microelectrolysis couples in situ electrochemical oxidation with particle-mediated algal separation for harmful algal bloom control. Here, the process was advanced for Heterosigma akashiwo through comparative mineral evaluation, electrolysis-pH regulation, and interaction analysis. Kaolinite gave the highest removal among four minerals (95.7%) and the largest apparent active chlorine adsorption amount, while time-resolved aggregate and clarification measurements linked this advantage to efficient particle-mediated cell capture and separation. Increasing initial electrolysis pH from 2 to 10 raised removal at 400 μL from 51.8% to >95% together with a larger post-electrolysis active chlorine inventory;92-93% of measured chlorine remained dissolved, and equal-C₀ tests showed comparable apparent adsorption across pH, supporting chlorine availability as the main factor governing apparent adsorption in the contact experiments. Independent dosing identified a super-additive window: 6 mg L-1 active chlorine plus 0.08 g L-1 kaolinite yielded 95.2% removal, 18.2 percentage points above Bliss independence. Oxidative and photosystem II responses linked process optimization to algal injury, establishing a parameterized oxidation-separation strategy for bloom control.
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