- Title
- Role of beryllium in the environment: Insights from specific sorption and precipitation studies under different conditions
- Creator
- Islam, Md. Rashidul; Sanderson, Peter; Payne, Timothy E.; Deb, Amal Kanti; Naidu, Ravi
- Relation
- Science of the Total Environment Vol. 838 Part 1, Issue 10 September 2022, no. 155698
- Publisher Link
- http://dx.doi.org/10.1016/j.scitotenv.2022.155698
- Publisher
- Elsevier
- Resource Type
- journal article
- Date
- 2022
- Description
- In this study, we examined factors influencing the environmental behaviour of Be, specifically considering soils collected from a legacy radioactive waste disposal site near Sydney (Australia). The precipitation study showed the formation of Be(OH)2 (amorphous) from ICP standard solution, but a mixture of Be(OH)2 (alpha), Be(OH)2 (beta) and ternary Na/S-Be (ΙΙ)-OH(s) solid phase were formed from BeSO4 solutions. The precipitation of Be started at relatively lower pH at higher concentrations than at the lower Be concentration as indicated by both laboratory data and simulation. Across the pH range, the Be sorption curve was divided into three phases, these being pH 3-6, pH 6-10, and pH > 10, within which sorption of Be with soil was 9-97%, 90-97%, and 66-90%, respectively. Beryllium solubility was limited at pH > 7, but a sorption study with soil showed chemisorption under both acidic and alkaline pH (pH 5.5 and 8) conditions, which was confirmed by FTIR and XPS analysis. At pH 5.5 (specifically relevant to the study site), sorption of Be was 72-95%, in which 77% and 46% Be was respectively sorbed by separated fulvic and humic acid fractions. The irreversible chemisorption mechanism was controlled by SOM at higher pH, and by metal oxyhydroxides at lower pH. Both organic and inorganic components synergistically influence the specific chemisorption of Be at the intermediate pH 5.5 of field soil.
- Subject
- beryllium hydrolysis; precipitation; environment; contaminated soil; specific chemisorption; SDG 12; Sustainable Development Goals
- Identifier
- http://hdl.handle.net/1959.13/1487673
- Identifier
- uon:52210
- Identifier
- ISSN:0048-9697
- Language
- eng
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