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Procedure to Evaluate the Efficiency of Flocculants for the Removal of Dispersed Particles from Plant Extracts
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Changes in Microcystis aeruginosa cell integrity and variation in microcystin-LR and proteins during Tanfloc
Jun Hou1, Zijun Yang1, Peifang Wang1
1Key Laboratory of Integrated Regulation and Resources Development on Shallow Lakes of Ministry of Education, College of Environment, Hohai University, Nanjing 210098, China.
Abstract:
The objective of this study was to determine the influence of Tanfloc on Microcystis aeruginosa cell integrity, microcystin-LR (MC-LR), and proteins during flocculation and floc storage. The effects of Tanfloc addition, stirring, and floc storage time were considered to minimize cell damage and the release of MC-LR and proteins. Optimal flocculation conditions (Tanfloc dosage 10.42 mg L-1, rapid agitation for 0.36 min at 568.88 rpm and slow agitation for 14.14 min at 12.1 rpm) were obtained using the response surface methodology. Up to 98.9% of the M. aeruginosa cells were removed intact at low Tanfloc dosage. During floc storage, Tanfloc initially protected the cells. After 8 d, large-scale cell lysis occurred because Tanfloc had substantially decomposed. Nevertheless, Tanfloc also extended the extracellular MC-LR and protein release time to 8 d. This delay ensured adequate time to decontaminate sludge containing the algae, thereby reducing the risk of secondary pollution. In addition, the low cost of Tanfloc facilitates its widespread application in the management of harmful algal blooms.
Insights
Tanfloc effectively removes intact Microcystis aeruginosa cells, protecting them during initial floc storage. This process delays toxin release, aiding in harmful algal bloom management and reducing secondary pollution risks.
Area of Science:
- Environmental Science
- Water Treatment
- Microbiology
Background:
- Harmful algal blooms (HABs) caused by cyanobacteria like Microcystis aeruginosa pose significant environmental and health risks.
- Microcystin-LR (MC-LR) is a potent toxin released during algal cell lysis, contaminating water sources.
- Effective removal and management of algal biomass are crucial for mitigating HAB impacts.
Purpose of the Study:
- To evaluate the impact of Tanfloc on Microcystis aeruginosa cell integrity, MC-LR, and protein release during flocculation and storage.
- To determine optimal flocculation conditions using Tanfloc to minimize cell damage and toxin release.
- To assess the protective effect of Tanfloc on algal cells and toxins during floc storage.
Main Methods:
- Response surface methodology (RSM) was employed to optimize Tanfloc dosage, rapid agitation, and slow agitation parameters.
- Microcystis aeruginosa cell integrity, MC-LR, and protein concentrations were monitored under various flocculation and storage conditions.
- Algal cell removal efficiency and lysis rates were quantified.
Main Results:
- Optimal flocculation conditions achieved up to 98.9% intact Microcystis aeruginosa cell removal with a low Tanfloc dosage.
- Tanfloc initially protected algal cells from lysis during floc storage.
- A delay in extracellular MC-LR and protein release was observed for up to 8 days due to Tanfloc's presence.
Conclusions:
- Tanfloc is effective in removing intact Microcystis aeruginosa cells and delaying the release of MC-LR and proteins.
- The extended delay in toxin release provides a critical window for sludge decontamination, reducing secondary pollution risks.
- The cost-effectiveness of Tanfloc supports its potential for widespread application in managing harmful algal blooms.
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07:18Natural Product Discovery with LC-MS/MS Diagnostic Fragmentation Filtering: Application for Microcystin Analysis
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