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1.
Surface sediment samples were collected at the West (east coast and west coast of Peninsular Malaysia) and East (Sabah and Sarawak) Malaysia in several expeditions within August 2003 until June 2008 for determining the level of natural radium isotopes. Activity concentrations of 226Ra and 228Ra in surface marine sediment at 176 sampling stations were measured. The activity concentrations of both radionuclides in Malaysia (East and West Malaysia) display varied with the range from 9 to 158 Bq/kg dry wt. and 13 to 104 Bq/kg dry wt., respectively. Meanwhile, the ratio distributions of 228Ra/226Ra were ranged from 0.62 to 3.75. This indicated that the ratios were slightly high at west coast of Peninsular Malaysia compared to other regions (east coast of Peninsular Malaysia, Sabah and Sarawak). The variation of activity concentrations of 226Ra and 228Ra and its ratios were also supported by the statistical analyses of one-way ANOVA and t test at 95 % confidence level, whereby there were proved that the measured values were different between the regions. These different were strictly related to their half-life, potential input sources (included their parents, 238U and 232Th), parent’s characteristic, the geological setting/formation of the study area, environment origin and behavior.  相似文献   

2.
The present occurrence of 226Ra and 228Ra in marine sediment core and fish from the Exclusive Economic Zone in the east coast of Peninsular Malaysia were studied. Sediment core and biota in respectively was collected using multicorer device and purchased from local fishermen at identified stations during the cruise expedition conducted in 2008. The purpose of this study was to determine and to make available an inventory of activity concentration levels and activity ratio for these radionuclides in this region. The activity concentrations of 226Ra and 228Ra in sediment core and edible part of fish were ranged between 15.9–46.5 and 27.7–87.1 Bq/kg dry wt and; 0.80–2.13 and <0.95–3.57 Bq/kg fresh wt, respectively. Meanwhile, the activity ratios of 228Ra/226Ra in sediment core and fish were varied with the range between 1.63–2.09 and 0.45–2.38, respectively. Refer to those ranges the activity concentrations of radium isotopes were comparable with other region. Thus, it can be concluded that the occurrence of radium isotopes mainly supplied from terrestrial sources and the factors of assimilation efficiency and transfer coefficient of radium may probably effect to the variation activity concentration of 226Ra and 228Ra and its activity ratio in edible part of pelagic and demersal fish obtained in this study.  相似文献   

3.
The most commonly available 226Ra determination was too time-consuming to be suited to 226Ra monitoring for the accidental release. The formula for determination of 226Ra was derived by 224Ra correction for WHO's equation. A rapid determination of 226Ra in environmental materials was made possible by using this formula. The 226Ra values of the soil and natural water at Ningyoh-Tohge obtained by the present method were in good agreement with those by the conventional WHO method. It was demonstrated that 226Ra of more than about 37 mBq (1 pCi) in the sample could be determined within 4 days by this method.  相似文献   

4.
Phosphogypsum discharges by phosphate-ore processing industries pollute sediments of the Rotterdam harbour area with226Ra. Direct measurement of this radionuclide in sediments does not provide a reliable indication of the elevation of the levels, since226Ra levels in sediments depend on the particle size. To eliminate the size effect, the226Ra/Ba ratio in sediments was tested as a possible indicator for the226Ra in the discharges. The results indicate almost a doubling of the226Ra levels in sediment samples due to phosphogypsum discharges. The contribution of phosphogypsum to the sediment mass was calculated in the order of a few percent equivalent.  相似文献   

5.
226Ra, 228Ra and 210Pb Isotopes in Some Water Samples of Mines   总被引:1,自引:0,他引:1  
A method for the determination of 226Ra, 228Ra and 210Pb in water samples of mining regions by measuring the and intensities with the help of a liquid scintillation counter is presented. The high-energy part of the -particle spectrum emitted by 210Bi is used for the determination of 210Pb content in the samples. An attempt is also given to explain the radioactive disequilibrium between 226Ra and 210Pb in the samples investigated.  相似文献   

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The chemical behavior of calcium, barium and radium in the ion exchange resins Dowex 50W-X8, AG 50W-X8 and Merk I in the presence of ammonium tartrate, EDTA, and citrate has been studied. No differences were observed in results while using any one of the three resins. Calcium, barium and radium were fixed to the exchange column at pH 4.8 EDTA solution. Calcium was eluted in an EDTA solution at pH 5.3, barium and radium between pH 8–11. Elution in citrate media for calcium was achieved at pH 6.1 and for radium at pH 10. In ammonium tartrate, calcium was eluted at pH 6, barium and radium at pH 11.5. Radium was also eluted from the ion exchange resins with a 2M nitric acid solution. The radium free of calcium was electrodeposited onto a stainless steel disc cathode using a 0.1 M potassium fluoride solution, pH 12–14, with a yield of >50%. The energies of226Ra were analyzed through high resolution -spectra. The226Ra utilized for these experiments was separated from Mexican carnotite.  相似文献   

8.
Summary The measurement of radium isotopes in natural waters is important for oceanographic studies and for public health reasons. Radium-226 (T1/2 = 1620 y) is one of the most toxic of the long-lived alpha-emitters present in the environment due to its long life and its tendency to concentrate in bones, which increases the internal radiation dose of individuals. The analysis of 226Ra and 228Ra in natural waters can be tedious and time-consuming. Different sample preparation methods are often required to prepare 226Ra and 228Ra for separate analyses. A rapid method has been developed at the Savannah River Environmental Laboratory that effectively separates both 226Ra and 228Ra (via 228Ac) for assay. This method uses MnO2 Resin from Eichrom Technologies (Darien, IL, USA) to preconcentrate 226Ra and 228Ra rapidly from water samples, along with 133Ba tracer. DGA Resinò (Eichrom) and Ln-Resinò (Eichrom) are employed in tandem to prepare 226Ra for assay by alpha-spectrometry and to determine 228Ra via the measurement of 228Ac by gas proportional counting. After preconcentration, the manganese dioxide is dissolved from the resin and passed through stacked Ln-Resin-DGA Resin cartridges that remove uranium and thorium interferences and retain 228Ac on DGA Resin. The eluate that passed through this column is evaporated, redissolved in a lower acidity and passed through Ln-Resin again to further remove interferences before performing a barium sulfate microprecipitation. The 228Ac is stripped from the resin, collected using cerium fluoride microprecipitation and counted by gas proportional counting. By using vacuum box cartridge technology with rapid flow rates, sample preparation time is minimized.  相似文献   

9.
The electrodeposition of226Ra for -spectrometry was reinvestigated to improve reproducibility and yield. Electrodeposition is from 20 ml of 90% propan-2-ol10% 0.05M HNO3 onto stainless steel disks, using 100 mA at 35 V for 20 minutes and a platinum anode. Half deposition time is 3–4 minutes. The following factors were found important: 1. Maintaining the same anode position. 2. Rotation of cathode. 3. Exclusion of sulphate. 4. Avoiding heating the HNO3/propan-2-ol plating solution. 5. Exclusion of solubilised resin resulting from passage through ion-exchange columns. 6. Maintaining other impurities at less than 10 g. If these precautions are followed yields are greater than 90%.  相似文献   

10.
A study of the immobilization for226Ra waste has been carried out. Cement-based concrete was used as a matrix for the solidification of radium waste. The experimental results show that the cement mixture with water/cement between 0.46–0.54 has higher strengh (above 20 MPa), and the compressive strength was not reduced by addition of 1% barite or the radium waste (RaSO4) into the concrete solid.Sponsored by the National Nuclear Corporation of China.  相似文献   

11.
A new rapid method for the determination of 226Ra in environmental samples has been developed at the Savannah River Site Environmental Lab (Aiken, SC, USA) that can be used for emergency response or routine sample analyses. The need for rapid analyses in the event of a Radiological Dispersive Device or Improvised Nuclear Device event is well-known. In addition, the recent accident at Fukushima Nuclear Power Plant in March, 2011 reinforces the need to have rapid analyses for radionuclides in environmental samples in the event of a nuclear accident. 226Ra (T1/2?=?1,620?years) is one of the most toxic of the long-lived alpha-emitters present in the environment due to its long life and its tendency to concentrate in bones, which increases the internal radiation dose of individuals. The new method to determine 226Ra in environmental samples utilizes a rapid sodium hydroxide fusion method for solid samples, calcium carbonate precipitation to preconcentrate Ra, and rapid column separation steps to remove interferences. The column separation process uses cation exchange resin to remove large amounts of calcium, Sr Resin to remove barium and Ln Resin as a final purification step to remove 225Ac and potential interferences. The purified 226Ra sample test sources are prepared using barium sulfate microprecipitation in the presence of isopropanol for counting by alpha spectrometry. The method showed good chemical recoveries and effective removal of interferences. The determination of 226Ra in environmental samples can be performed in less than 16?h for vegetation, concrete, brick, soil, and air filter samples with excellent quality for emergency or routine analyses. The sample preparation work takes less than 6?h. 225Ra (T1/2?=?14.9?day) tracer is used and the 225Ra progeny 217At is used to determine chemical yield via alpha spectrometry. The rapid fusion technique is a rugged sample digestion method that ensures that any refractory radium particles are effectively digested. The preconcentration and column separation steps can also be applied to aqueous samples with good results.  相似文献   

12.
A procedure for the determination of natural uranium and226Ra in waters and soils has been carried out and applied to the analysis of samples for environmental radiological monitoring.226Ra determination consists of co-precipitation with BaSO4,222Rn emanation in toluene and finally liquid scintillation counting. Natural uranium is then determined by a fluorometric technique. This paper describes the method and the conditions that were tested to optimize it. The technique was found to be suitable for the analysis of surface and ground waters, samples from rivers, streams and lakes and soil samples, because of its few steps, short processing time, high recovery percentages and suitable detection limits.  相似文献   

13.
An investigation on the distribution of 226Ra and 228Ra activity concentration in coastal surface sea water from Okha in Gujarat to Ratnagiri in Maharashtra state along the west coast of India was carried out. In-situ pre-concentration technique was used to measure radium isotopes by passing 1,000 L of seawater through MnO2 impregnated polypropylene filter cartridges at all the locations. 226Ra was estimated using gamma ray peak of its daughter radionuclides 214Bi and 214Pb. 228Ra was estimated from its daughter 228Ac. In the coastal waters, 226Ra and 228Ra activity concentration were observed to be in the range of 1.5–2.9 and 2.5–8.6 Bq m?3 with a mean of 2.2 and 4.9 Bq m?3 respectively. The activity of 228Ra was observed to be more than 226Ra in all the locations. The variation in spatial distribution of the radium isotopes activity concentration and its ratio with respect to location is discussed in the paper. The radioactive database obtained represents reference values for coastal environment of India.  相似文献   

14.
The concentration of Ra isotopes in environmental water can be determined from the amount of Ra isotopes recovered in two successive batch operations a using cation exchange resin. The present analytical method is applicable to 10 liter of sample water having a Ra concentration larger than 10 mBq/l and is also applicable to the ordinary underground water of less than 1 mBq/l by use of 50 liter of sample water. In case where Ra concentration is extremely low, Mn-impregnated acrylic fiber can be used with a larger volume of water sample as an absorbent by soaking it in the water.  相似文献   

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Natural radioactivity measurements and assessment of radiological hazards in soil and sand samples obtained from Penang, Malaysia were carried out using the Exploranium GR-135 Plus “Identifier” Radioisotope Identification Device and high-resolution High Purity Germanium (HPGe) detector system. The activity concentrations of 238U, 226Ra, 232Th, and 40K were found to be 184±11, 396±22, 165±14, and 835±28 Bq kg?1 respectively, and the external gamma dose rate is 315±44 nGy h?1 for soil samples. For sand samples, the activity concentrations of 238U, 226Ra, 232Th and 40K were 31±8, 62±16, 36±6, and 369±17 Bq kg?1, respectively, and the external gamma dose rate is 66±12 nGy h?1. To assess the radiological hazard of radioactivity present in the samples, the radium equivalent activity, annual effective dose, annual gonadal dose equivalent, external hazard, and internal indices were calculated.The Raeq values of soil samples were higher than the limit of 370 Bq kg?1, which is equivalent to a gamma dose of 1.5 mSv yr?1, whereas the Raeq for sand samples was lower than 370 Bq kg?1. The calculated concentrations by HPGe spectroscopy were compared with the measured concentrations detected by a GR-135 spectrometer. The calculated and measured gamma dose rates had an ideal correlation coefficient R of 0.72. The gamma dose rates in Penang increased with the average annual age-standardized rates (ASR) for all cancers between 1994 and 2010. The effects of the pH value of soil and sand samples on natural radionuclides concentrations were investigated. The high concentration of 226Ra/238U ratio disequilibrium (226Ra/238U of 1.76–2.33) was observed in the sampling sites. Moreover, a portable continuous radon monitor (SNC, model 1029, Sun Nuclear Corporation) was used to measure the radon concentration of the soil surface. The radon concentrations were found to vary from 7 to 50 Bq m?3. A positive correlation was observed between the radon and radium concentrations in samples measured by the SNC continuous radon monitor and HPGe detector.  相似文献   

17.
A new method has been developed at the Savannah River National Laboratory (SRNL) that can be used for the rapid determination of 226Ra in emergency urine samples following a radiological incident. If a radiological dispersive device event or a nuclear accident occurs, there will be an urgent need for rapid analyses of radionuclides in urine samples to ensure the safety of the public. Large numbers of urine samples will have to be analyzed very quickly. This new SRNL method was applied to 100 mL urine aliquots, however this method can be applied to smaller or larger sample aliquots as needed. The method was optimized for rapid turnaround times; urine samples may be prepared for counting in <3 h. A rapid calcium phosphate precipitation method was used to pre-concentrate 226Ra from the urine sample matrix, followed by removal of calcium by cation exchange separation. A stacked elution method using DGA Resin was used to purify the 226Ra during the cation exchange elution step. This approach combines the cation resin elution step with the simultaneous purification of 226Ra with DGA Resin, saving time. 133Ba was used instead of 225Ra as tracer to allow immediate counting; however, 225Ra can still be used as an option. The rapid purification of 226Ra to remove interferences using DGA Resin was compared with a slightly longer Ln Resin approach. A final barium sulfate micro-precipitation step was used with isopropanol present to reduce solubility; producing alpha spectrometry sources with peaks typically <40 keV FWHM (full width half max). This new rapid method is fast, has very high tracer yield (>90 %), and removes interferences effectively. The sample preparation method can also be adapted to ICP-MS measurement of 226Ra, with rapid removal of isobaric interferences.  相似文献   

18.

The activity concentrations of 226Ra, 228Ra and 222Rn were measured in 87 groundwater samples to estimate the activity concentrations of these radionuclides and health impact due to intake of these radionuclides in groundwater of Jordan. The mean activity concentrations of 226Ra, 228Ra and 222Rn in groundwater were found to be 0.293?±?0.005 Bq L?1, 0.508?±?0.009 Bq L?1 and 58.829?±?8.824 Bq L?1, respectively. They give a mean annual effective dose of 0.481 mSv with mean lifetime risk of 24.599?×?10?4, exceeding the admissible limit of 10?4. Most of the received annual effective dose (59.15% of the total) is attributed to 228Ra.

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