Evaluating the role of re-adsorption of dissolved Hg2+ during cinnabar dissolution using isotope tracer technique
Creators
- 1. Department of Chemistry and Biochemistry, Florida International University, Miami, FL 33199 (United States)
- 2. Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education/Qingdao Collaborative Innovation Center of Marine Science and Technology, Ocean University of China, Qingdao 266100 (China)
- 3. Southeast Environmental Research Center, Florida International University, Miami, FL 33199 (United States)
- 4. College of Life Sciences, Fujian Agriculture and Forestry University, Fuzhou 350002 (China)
- 5. Applied Research Center, Florida International University, Miami, FL 33199 (United States)
- 6. State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China)
- 7. Environmental Sciences Division, Oak Ridge National Laboratory, Oak Ridge TN 37831 (United States)
Description
Highlights: • Develop a new method to study Hg re-adsorption in cinnabar. • Both isotope dilution and tracer techniques were adopted. • The presence of O2 can significantly enhance the dissolution of cinnabar. • Prove the necessity of including re-adsorption in estimating cinnabar dissolution. - Abstract: Cinnabar dissolution is an important factor controlling mercury (Hg) cycling. Recent studies have suggested the co-occurrence of re-adsorption of the released Hg during the course of cinnabar dissolution. However, there is a lack of feasible techniques that can quantitatively assess the amount of Hg re-adsorbed on cinnabar when investigating cinnabar dissolution. In this study, a new method, based on isotope tracing and dilution techniques, was developed to study the role of Hg re-adsorption in cinnabar dissolution. The developed method includes two key components: (1) accurate measurement of both released and spiked Hg in aqueous phase and (2) estimation of re-adsorbed Hg on cinnabar surface via the reduction in spiked 202Hg2+. By adopting the developed method, it was found that the released Hg for trials purged with oxygen could reach several hundred μg L−1, while no significant cinnabar dissolution was detected under anaerobic condition. Cinnabar dissolution rate when considering Hg re-adsorption was approximately 2 times the value calculated solely with the Hg detected in the aqueous phase. These results suggest that ignoring the Hg re-adsorption process can significantly underestimate the importance of cinnabar dissolution, highlighting the necessity of applying the developed method in future cinnabar dissolution studies.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jhazmat.2016.05.084Additional details
Identifiers
- DOI
- 10.1016/j.jhazmat.2016.05.084;
- PII
- S0304-3894(16)30529-5;
Publishing Information
- Journal Title
- Journal of Hazardous Materials
- Journal Volume
- 317
- Journal Page Range
- p. 466-475
- ISSN
- 0304-3894
- CODEN
- JHMAD9
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48046898
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S07: ISOTOPES AND RADIATION SOURCES;
- Resource subtype / Literary indicator
- Numerical Data
- Descriptors DEI
- ADSORPTION; DISSOLUTION; EXPERIMENTAL DATA; ISOTOPE DILUTION; MERCURY IONS; SULFIDE MINERALS
- Descriptors DEC
- CHARGED PARTICLES; DATA; INFORMATION; IONS; ISOTOPE APPLICATIONS; MINERALS; NUMERICAL DATA; SORPTION; TRACER TECHNIQUES
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.