MSFIA-LOV system for 226Ra isolation and pre-concentration from water samples previous radiometric detection
- 1. Environment and Energy Department, Advanced Materials Research Center (CIMAV) S.C., Miguel de Cervantes 120, Chihuahua, Chih. 31136 (Mexico)
- 2. Environmental Radioactivity Laboratory (LaboRA), University of the Balearic Islands, Cra. Valldemossa km 7.5, 07122, Palma (Spain)
- 3. Department of Chemistry, University of the Balearic Islands, Cra. Valldemossa km 7.5, 07122, Palma (Spain)
Description
An automatic system based on multisyringe flow injection analysis (MSFIA) and lab-on-valve (LOV) flow techniques for separation and pre-concentration of 226Ra from drinking and natural water samples has been developed. The analytical protocol combines two different procedures: the Ra adsorption on MnO2 and the BaSO4 co-precipitation, achieving more selectivity especially in water samples with low radium levels. Radium is adsorbed on MnO2 deposited on macroporous of bead cellulose. Then, it is eluted with hydroxylamine to transform insoluble MnO2 to soluble Mn(II) thus freeing Ra, which is then coprecipitated with BaSO4. The 226Ra can be directly detected in off-line mode using a low background proportional counter (LBPC) or through a liquid scintillation counter (LSC), after performing an on-line coprecipitate dissolution. Thus, the versatility of the proposed system allows the selection of the radiometric detection technique depending on the detector availability or the required response efficiency (sample number vs. response time and limit of detection). The MSFIA-LOV system improves the precision (1.7% RSD), and the extraction frequency (up to 3 h−1). Besides, it has been satisfactorily applied to different types of water matrices (tap, mineral, well and sea water). The 226Ra minimum detectable activities (LSC: 0.004 Bq L−1; LBPC: 0.02 Bq L−1) attained by this system allow to reach the guidance values proposed by the relevant international agencies e.g. WHO, EPA and EC. - Highlights: • Automatic, rapid and selective method for 226Ra extraction/pre-concentration from water. • MSFIA-LOV system performs a sample clean-up prior to 226Ra radiometric detection. • 226Ra sample preparation allows using two radiometric detectors (LBPC and LSC). • Environmental levels of 226Ra are easily quantified. • High sensitivity and selectivity are achieved, reaching the 226Ra regulations for drinking water.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.aca.2016.01.004Additional details
Identifiers
- DOI
- 10.1016/j.aca.2016.01.004;
- PII
- S0003-2670(16)30026-5;
Publishing Information
- Journal Title
- Analytica Chimica Acta
- Journal Volume
- 911
- Journal Page Range
- p. 75-81
- ISSN
- 0003-2670
- CODEN
- ACACAM
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48002183
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ADSORPTION; BARIUM SULFATES; CELLULOSE; CONCENTRATION RATIO; COPRECIPITATION; DETECTION; DISSOLUTION; DRINKING WATER; EXTRACTION; HYDROXYLAMINE; LIQUID SCINTILLATION DETECTORS; MANGANESE OXIDES; PROPORTIONAL COUNTERS; RADIOCHEMICAL ANALYSIS; RADIOCHEMISTRY; RADIUM; RADIUM 226; SAMPLE PREPARATION; SEAWATER; SENSITIVITY
- Descriptors DEC
- ALKALINE EARTH ISOTOPES; ALKALINE EARTH METAL COMPOUNDS; ALKALINE EARTH METALS; ALPHA DECAY RADIOISOTOPES; AMINES; BARIUM COMPOUNDS; CARBOHYDRATES; CARBON 14 DECAY RADIOISOTOPES; CHALCOGENIDES; CHEMICAL ANALYSIS; CHEMISTRY; DIMENSIONLESS NUMBERS; ELEMENTS; EVEN-EVEN NUCLEI; HEAVY ION DECAY RADIOISOTOPES; HEAVY NUCLEI; HYDROGEN COMPOUNDS; ISOTOPES; MANGANESE COMPOUNDS; MEASURING INSTRUMENTS; METALS; NUCLEI; ORGANIC COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; POLYSACCHARIDES; PRECIPITATION; QUANTITATIVE CHEMICAL ANALYSIS; RADIATION DETECTORS; RADIOISOTOPES; RADIUM ISOTOPES; SACCHARIDES; SCINTILLATION COUNTERS; SEPARATION PROCESSES; SORPTION; SULFATES; SULFUR COMPOUNDS; TRANSITION ELEMENT COMPOUNDS; WATER; YEARS LIVING RADIOISOTOPES
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.