<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhan Z</submitter><funding>Shenzhen Science and Technology Innovation Commission</funding><funding>Natural Science Foundation of Guangdong Province (Guangdong Natural Science Foundation)</funding><pagination>100</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12775475</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(1)</volume><pubmed_abstract>Lime-based precipitation, though widely adopted for wastewater phosphorus (P) removal, suffers from surface passivation. The passivation layer inhibits Ca&lt;sup>2+&lt;/sup> release, forcing excessive dosing while yielding low-quality sludge and effluent with elevated hardness and pH. Limestone, despite its economic and environmental benefits, exhibits limited efficacy under fluctuating alkalinity. Here, we develop a limestone-integrated electrochemical system that spatially decouples the dissolution and precipitation reactions. By strategically positioning limestone at the acidic anode, we ensure sustained Ca&lt;sup>2+&lt;/sup> release without passivation, while cathodic alkalinity enables efficient P recovery (85.7%). The system produces high-purity products (15.2 wt% P) at low energy consumption (14.8 kWh kg P&lt;sup>-1&lt;/sup>) and delivers superior effluent quality. Beyond its robustness and capacity flexibility over long-term operation, the electrochemical strategy reduces overall costs by 73.2% and carbon emissions by 29.1%, positioning it as a cost-effective and sustainable alternative to traditional lime-based wastewater treatment with remarkable passivation resistance and resource recovery efficiency.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Spatially decoupled electrochemical strategy for lime passivation prevention and sustainable phosphate recovery.</pubmed_title><pmcid>PMC12775475</pmcid><funding_grant_id>JCYJ20250604144607011</funding_grant_id><funding_grant_id>JCYJ20230807093405011</funding_grant_id><funding_grant_id>2023A1515110152</funding_grant_id><pubmed_authors>Lv J</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Lei Y</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Zhan Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Spatially decoupled electrochemical strategy for lime passivation prevention and sustainable phosphate recovery.</name><description>Lime-based precipitation, though widely adopted for wastewater phosphorus (P) removal, suffers from surface passivation. The passivation layer inhibits Ca&lt;sup>2+&lt;/sup> release, forcing excessive dosing while yielding low-quality sludge and effluent with elevated hardness and pH. Limestone, despite its economic and environmental benefits, exhibits limited efficacy under fluctuating alkalinity. Here, we develop a limestone-integrated electrochemical system that spatially decouples the dissolution and precipitation reactions. By strategically positioning limestone at the acidic anode, we ensure sustained Ca&lt;sup>2+&lt;/sup> release without passivation, while cathodic alkalinity enables efficient P recovery (85.7%). The system produces high-purity products (15.2 wt% P) at low energy consumption (14.8 kWh kg P&lt;sup>-1&lt;/sup>) and delivers superior effluent quality. Beyond its robustness and capacity flexibility over long-term operation, the electrochemical strategy reduces overall costs by 73.2% and carbon emissions by 29.1%, positioning it as a cost-effective and sustainable alternative to traditional lime-based wastewater treatment with remarkable passivation resistance and resource recovery efficiency.</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-09T05:30:31.512Z</modification><creation>2026-06-09T03:07:53.303Z</creation></dates><accession>S-EPMC12775475</accession><cross_references><pubmed>41495040</pubmed><doi>10.1038/s41467-025-67911-1</doi></cross_references></HashMap>