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1.
The concentration of99Tc in IAEA reference materials has been determined with an ICP-MS as 0.86±0.07 Bq·kg−1 dry for IAEA-373 (grass) and 0.25±0.02 Bq·kg−1 dry for IAEA-375 (soil). These being sufficiently higher than the detection limits of typical measurement methods, both materials can be used as reference materials for determining low-level99Tc in environmental samples.  相似文献   

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Three environmental matrices proposed as Certified Reference Materials, issued by the EU Standards, Measurement and Testing Programme (SMTP) formerly Bureau Communautaire de Reference (BCR) have been characterized for their trace element contents.The materials are: BCR 277 R Estuarine Sediment, BCR 280 R Lake Sediment and BCR 320 R Channel Sediment.Several trace elements, including As, Co, Cr, Fe, Mn, Ni, Sb, Sc, Th, U and Zn have been determined by our laboratory using Instrumental Neutron Activation Analysis (INAA). Our contributed values are being considered for the final certification.  相似文献   

4.
A certified reference material (CRM) for radionuclides in seawater, IAEA-381 (Irish Sea Water), is described and the results of certification are presented. The material has been certified for nine radionuclides (40K, 90Sr, 137Cs, 237Np, 238Pu, 239Pu,240Pu, 239,240Pu and 241Am). Information on massic activities with the corresponding 95% confidence intervals are given for eight radionuclides (3H, 125Sb, 234U, 235U, 236U, 238U, 241Pu and 244Cm). Less reported radionuclides include 60Co, 99Tc, and 242Pu. The CRM may be used for quality assurance/quality control of the analysis of radionuclides in environmental water samples, for the development and validation of analytical methods and for training purposes. The material is available from the IAEA in 5 kg units.  相似文献   

5.
Due to the increased demand for new reference materials certified for total and methylmercury (MeHg) a sample of mussel homogenate (IAEA-142) has been prepared. Thirteen experienced laboratories reported results for total Hg of which 9 laboratories also reported results for MeHg content. Laboratories reporting MeHg results used various isolation techniques (solvent extraction, saponification, acid leaching, ion-exchange separation, and distillation) and detection systems (cold vapour atomic absorption spectrometry (CV AAS), cold vapour atomic fluorescence spectrometry (CV AFS), gas chromatography with electron capture detector (GC/ECD) and HPLC with CV AAS detector). In the case of total Hg, most of the laboratories used acid digestion, only two used alkaline dissolution, followed either by CV AAS or CV AFS. One laboratory used neutron activation analyses with radiochemical separation. The data received were in good agreement. The value for total Hg was certified to be 126 ng/g, with a 95% confidence interval from 119 to 132 ng/g. For MeHg the certified value of 47 ng/g expressed as Hg was assigned, with a 95% confidence interval from 43 to 51 ng/g. Stability testing has shown that both total and MeHg are stable if samples are stored in a dry and dark place at room temperature. The sample is now available as a certified reference material and is, in particular, useful for quality control measurements of Hg and MeHg in mussel samples at low concentration levels. Received: 24 September 1996 / Revised: 20 November 1996 / Accepted: 8 December 1996  相似文献   

6.
Due to the increased demand for new reference materials certified for total and methylmercury (MeHg) a sample of mussel homogenate (IAEA-142) has been prepared. Thirteen experienced laboratories reported results for total Hg of which 9 laboratories also reported results for MeHg content. Laboratories reporting MeHg results used various isolation techniques (solvent extraction, saponification, acid leaching, ion-exchange separation, and distillation) and detection systems (cold vapour atomic absorption spectrometry (CV AAS), cold vapour atomic fluorescence spectrometry (CV AFS), gas chromatography with electron capture detector (GC/ECD) and HPLC with CV AAS detector). In the case of total Hg, most of the laboratories used acid digestion, only two used alkaline dissolution, followed either by CV AAS or CV AFS. One laboratory used neutron activation analyses with radiochemical separation. The data received were in good agreement. The value for total Hg was certified to be 126 ng/g, with a 95% confidence interval from 119 to 132 ng/g. For MeHg the certified value of 47 ng/g expressed as Hg was assigned, with a 95% confidence interval from 43 to 51 ng/g. Stability testing has shown that both total and MeHg are stable if samples are stored in a dry and dark place at room temperature. The sample is now available as a certified reference material and is, in particular, useful for quality control measurements of Hg and MeHg in mussel samples at low concentration levels.  相似文献   

7.
Selenomethionine content of candidate reference materials   总被引:1,自引:0,他引:1  
Selenium has been identified as an antioxidant of importance in the diet. Accurate determination of its chemical forms depends on the availability of suitable reference materials (RMs). Two candidate reference materials for determination of selenomethionine (Semet) in food-related materials, a standard wheat gluten sample (NIST RM 8418 Wheat Gluten) and a commercial selenium enriched yeast, have been examined by use of a gas chromatography–isotope dilution mass spectrometry (IDMS) procedure, after treatment of the matrix with 0.1 mol L–1 hydrochloric acid containing stannous chloride, addition of CNBr, and extraction with chloroform. This procedure results in cleavage of the CH3Se group to form volatile CH3SeCN. Addition of isotopically enriched 74Semet to an analytical sample enables estimation of the naturally occurring protein-bound 80Semet by IDMS without a protein-digestion process. We found that the Wheat Gluten RM contains a significant amount of Semet as a portion of its assigned value of 2.58 μg Setotal g–1. Commercial selenium yeast tablets are labeled as containing an elevated level of “organic selenium”, usually as Semet. The sample we investigated contained 210 μg Setotal g–1 sample as determined separately by IDMS, measuring elemental selenium after digestion. 73% of this total (153±21 μg SeSemet g–1; n = 23) was present as Semet. Thus, these two materials contain significant amounts of their total selenium content as Semet and would be good candidates for further study and characterization as reference materials for determining this important food component. The CNBr reaction used will also enable the determination of Se-(methyl)selenocysteine, the biological role of which is of recent interest. In addition to matrix RMs for Semet, it is important to have standard materials of the pure substance. We have examined a sample of a candidate standard material of selenomethionine being prepared by the USP. It was confirmed that this material is pure selenomethionine. Received: 13 December 2000 / Revised: 5 March 2001 / Accepted: 12 March 2001  相似文献   

8.
Summary Very few biological reference materials are certified for nickel below 1 mg · kg–1. Neutron activation analysis was only rarely considered as a possible approach; reported sensitivities were usually not very good, unless preconcentration was applied.In the present work, the relatively high fast neutron flux of our TRIGA reactor was used to induce the 58Ni(n, p)58Co reaction, and 58Co (E =811 keV) was radiochemically separated from other radionuclides by classical anion-exchange chromatography in hydrochloric acid. 57Co was added to the irradiated sample before decomposition as a radioisotopic yield monitor. By concentrating the final sample fraction and measurement in a well-type HP Ge detector, Ni concentrations down to the 10-g · kg–1 level could be determined for samples irradiated for 1 day. 60Co, produced by neutron capture on 59Co, is also coseparated and quantified from the gamma spectrum, so that both elements Ni and Co are determined. Results are reported for a series of NBS and other biological reference materials in the concentration range 10 g-10 mg · kg–1. Possibilities for further increases in sensitivity are discussed.
Spurenbestimmung von Nickel (und Cobalt) in biologischen Referenzmaterialien durch radiochemische Neutronenaktivierungsanalyse
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9.
Trace element contents from effluents of a simulated coal-fired magnetohydrodynamic (MHD) combustion process have been determined using thermal neutron activation analysis techniques. The quality control consisted of replicate analyses of standard rock (G-2) for precision and accuracy determination. The concentration of elements in various samples were fairly constant throughout the process stream. Elemental ratios of trace elements at one sampling position (SDA) are presented but cannot easily be explained. However, the high concentration of arsenic in SDA was attributed to incomplete separation of slag from the adhering lining. Potassium concentration in the thickener tank was consistent with the solubility of potassium salts and the data support possible recovery mechanisms.  相似文献   

10.
Neutron activation analysis (INAA) has been applied to multielemental determination of eleven medicinal plants used to cure the urinary tract diseases observed in Algeria. These plants include Androgena Citratus, Ceratonia Siliquata, Punica Granatum, Glyryrrhiza Glabra, Lausaunia Alba, Fragaria Vesca, Arbutus Unedol, Hordeum Vulgaris, Papieteria Officinalis, Zea Mays L, and Davallia Seae. Concentrations of twenty elements Ba, Br, Ca, Cl, Co, Cu, Cr, Fe, I, Mn, Na, Mg, Rb, Sb, Se, Sc, Sr, Ti, V, and Zn have been determined by short, and long irradiation times with a thermal and epithermal flux of 1.4·1012 n·cm−2·s−1 and 1.4·1011 n·cm−2·s−1, respectively. These analyses were performed in conjunction with Compton suppression. In almost herbs studied the Co, Cr, Cu, Rb, Sb, Sc, Se and V are found to be present at trace levels, Br, Mn, and Zn at the minor level, and Ca, Cl, Fe, Mg and Na are generally at the major level. The accuracy of the measurements has been evaluated by analyzing NIST-botanical references materials.  相似文献   

11.
12.
Selenium has been identified as an antioxidant of importance in the diet. Accurate determination of its chemical forms depends on the availability of suitable reference materials (RMs). Two candidate reference materials for determination of selenomethionine (Semet) in food-related materials, a standard wheat gluten sample (NIST RM 8418 Wheat Gluten) and a commercial selenium enriched yeast, have been examined by use of a gas chromatography-isotope dilution mass spectrometry (IDMS) procedure, after treatment of the matrix with 0.1 mol L(-1) hydrochloric acid containing stannous chloride, addition of CNBr, and extraction with chloroform. This procedure results in cleavage of the CH3Se group to form volatile CH3SeCN. Addition of isotopically enriched 74Semet to an analytical sample enables estimation of the naturally occurring protein-bound 80Semet by IDMS without a protein-digestion process. We found that the Wheat Gluten RM contains a significant amount of Semet as a portion of its assigned value of 2.58 microg Se(total g(-1). Commercial selenium yeast tablets are labeled as containing an elevated level of "organic selenium", usually as Semet. The sample we investigated contained 210 microg Se(total) g(-1) sample as determined separately by IDMS, measuring elemental selenium after digestion. 73% of this total (153 +/- 21 microg Se(semet) g(-1); n = 23) was present as Semet. Thus, these two materials contain significant amounts of their total selenium content as Semet and would be good candidates for further study and characterization as reference materials for determining this important food component. The CNBr reaction used will also enable the determination of Se-(methyl)selenocysteine, the biological role of which is of recent interest. In addition to matrix RMs for Semet, it is important to have standard materials of the pure substance. We have examined a sample of a candidate standard material of selenomethionine being prepared by the USP. It was confirmed that this material is pure selenomethionine.  相似文献   

13.
The proposed reference material from the International Atomic Energy Agency, namely IAEA-407 (Fish Homogenate) was analyzed using instrumental neutron activation analysis (INAA). 15 elements, Al, As, Cl, Co, Cr, Fe, Hg, Mg, Mn, K, Na, Sb, Se, V and Zn, were determined using two irradiations (5 minutes and 5 hours) and four countings. IAEA-MA-A-1/TM (Copepoda Homogenate), NIST-SRM-1566 (Oyster Tissue), NIST-SRM-1572 (Citrus Leaves) and NIST-SRM-1577a (Bovine Liver) were utilized as standards in the quantification step.  相似文献   

14.
Instrumental neutron activation analysis /INAA/ method was applied to measure major, minor and trace elements in 34 samples of hard and brown coal originating from eight Polish coal mines. The elemental concentrations of 38 elements /Na, Mg, Al, Cl, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, As, Se, Br, Rb, Sr, Mo, Ag, Cd, In, Sb, I, Cs, Ba, La, Ce, Sm, Eu, Lu, W, Au and Th/ are presented and compared with published data for coals from various origin. Enrichment factors, calculated relative to iron and the average crustal rock composition, indicated that several elements are highly enriched in Polish coals.  相似文献   

15.
It has been shown, for a Pb isotopic reference material and for natural Cd, that total evaporation with integrating mass spectrometric measurement allows the determination of isotope ratios of these elements with sufficient accuracy and reproducibility. It is possible to use the method in carefully selected cases for IDA-TIMS measurements without the application of bias factors derived from isotopic reference material measurements. IDA-TIMS measurements were used for the determination of Cd (40–400 g/g) in polyethylene and Cd (10 g/g), Pb (500 g/g), Ga (150 g/g) and Zn (2000 g/g) in the Al alloy AlCuMg2. Relative standard deviations (n=5) were between 1.2% to 2.4% in the first case and 0.3% for Cd, 0.4% for Ga, 0.14% for Pb, 0.6% for Zn in the second. Deviations from the certified values were between 0.8% and 1.4% in the first case. The four concentration values contributed to the AlCuMg2 certification measurements but deviated from the finally certified values as follows: Cd+1.0%, Ga–1.6%, Pb–0.9% and Zn+10%.  相似文献   

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17.
A new certified reference material (CRM) for radionuclides in sea water from the Irish sea (IAEA-443) is described and the results of the certification process are presented. Ten radionuclides (3H, 40K, 90Sr, 137Cs, 234U, 235U, 238U, 238Pu, 239+240Pu and 241Am) have been certified, and information values on massic activities with 95% confidence intervals are given for four radionuclides (230Th, 232Th, 239Pu and 240Pu). Results for less frequently reported radionuclides (99Tc, 228Th, 237Np and 241Pu) are also reported. The CRM can be used for quality assurance/quality control of the analysis of radionuclides in water samples, for the development and validation of analytical methods and for training purposes. The material is available in 5 L units from IAEA (http://nucleus.iaea.org/rpst/index.htm).  相似文献   

18.
A new Reference Material (RM) for radionuclides in mussel (Mytilus galloprovincialis) from the Mediterranean Sea (IAEA-437) is described and the results of the certification process are presented. Four radionuclides (40K, 234U, 238U, and 239+240Pu) have been certified, and information values on massic activities with 95% confidence intervals are given for nine radionuclides (137Cs, 210Pb(210Po), 226Ra, 228Ra, 228Th, 230Th, 232Th, 235U, and 241Am). Results for less frequently reported radionuclides (90Sr, 129I, 238Pu, 239Pu, and 240Pu) are also reported. The RM can be used for quality assurance/quality control of the analysis of radionuclides in mussel samples, for the development and validation of analytical methods and for training purposes. The material is available in 200 g units.  相似文献   

19.
Selection criteria for production of food reference materials need to simultaneously consider realistic proximate matrix compositions, emerging trends for the nutritional and toxicological effects of less-emphasized trace elements (e.g., B, Li, Si, and V), chemical speciation (especially for As, Hg, Se, and Sn), and analyte certification requirements from the analyst's point of view. For the most part, currently available Certified Reference Materials (CRMs) do not meet many of these needs. Candidate CRMs with relevant concentrations of trace elements could be chosen from similar foods with different proximate compositions (e.g., fat content of milk products, meat, or soya flour). Explicit guidance must accompany CRMs so that variations in measured trace element concentrations arising from procedural lapses and basis weight are avoided.  相似文献   

20.
Analyses of freshwater are routinely performed by a number of organisations to monitor the levels of major elements. In order to improve and control the quality of such determinations, the Community Bureau of Reference (BCR) has organised a certification campaign to produce two reference materials (CRM 398, low element content and CRM 399, high element content) certified for their contents of Al, Ca, Cl, Fe, Mg, Mn, K, Na, P and S. These materials were carefully prepared (addition of the elements mentioned in the form of ammonium salts or nitrates to silica free deionised water) and their homogeneity and long term stability were verified. This paper presents the certification work performed.  相似文献   

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