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Samples Containing Strontium or BariumSample Preparation Guide: Part 6The MetalsNote: Ba and Sr will be treated collectively due to very similar chemistries. Both barium (Ba) and strontium (Sr) are silvery white metals resembling aluminum. The metals are unstable in air and burn with incandescence in moist air or when heated. They decompose water, evolving H2 and forming Ca(OH)2 or Ba(OH)2. The same reaction occurs more readily in acids—exercise caution. Oxides, Hydroxides, CarbonatesThe oxides are white and are obtained by ignition of the hydroxide, carbonate, nitrate, oxalate and all of their organic salts. The oxides, hydroxides and carbonates are all readily soluble in dilute acids combining to form the ions of the corresponding salt. They absorb CO2 from the air, becoming carbonates. In moist air, oxides become hydroxides, with the generation of heat if sufficient water is present. The hydroxides dissolve readily in dilute acids and are much more soluble in water than the corresponding Ca hydroxide. The oxide, hydroxide and carbonate are all readily soluble in dilute acids. Most analysts prefer dilute (1:1) nitric acid. Minerals and OresSince the ores contain such a wide assortment of other elements it is considered best to prepare them by fusion with either lithium carbonate in graphite crucibles or sodium carbonate in Pt crucibles. If barium sulfate is present, the fusion converts it to the barium carbonate and the corresponding sodium sulfate, which can be leached out from the fuseate with water prior to dissolution of the fuseate in dilute HCl. The following method is for the preparation of limestone for Ca, Mg, Fe, Al, Mn and Si using a lithium carbonate fusion but can be applied to samples high in Sr and Ba: Sample Preparation Procedure. The following is a general guide for sodium carbonate fusions:
When Ba is associated with sulfate as BaSO4 or the fluoride, it is suggested that the analyst fuse the sample with H3BO3 or B2O3 . This fusion is carried out in Pt crucibles at 1000 °C where the sample to flux ratio is at least 1:8 and can be as high as 1:30. The SO3 is expelled due to the high temperature of the acidic melt. The MF2 is opened out by this fusion procedure and the fluoride is tied up with the boron, making the dissolution of the fuseate in water or dilute acid possible without reformation of the MF2. Lithium tetraborate (Li2B4O7) has also proven to be a very useful way of opening out many of the ores associated with Ba and Sr. This fusion is carried out in Pt for ~10 minutes at 1000 °C and the fuseate is dissolved at room temperature by stirring with dilute (5% v/v) nitric acid. When metal ions that are readily hydrolyzed are present, dissolution in the presence of EDTA in 0.01 M HCl is advantageous. AlloysThe Ba and Sr metals are not used to a great extent nor are their alloys. Although commercial alloys are relatively rare, their dissolution can be affected using dilute nitric or nitric/HCl mixtures. Organic MatricesThese include a wide variety of materials including oil additives (Ba), petroleum matrices, coal, organic plant material, biological material, synthetic organics, etc. Samples can be digested with nitric/perchloric. For more detailed information about acid digestions of organics, please see the following article: Acid Digestions of Organic Samples. It is also very acceptable to dry ash organic samples for Ba or Sr analysis in a Pt crucible and then bring the resulting oxides into solution using a sodium carbonate fusion or if Ba or Sr alone are sought, dissolution in dilute nitric or HCl. For more information, see the portion of our Trace Analysis Guide that discusses Ashing. Hydrolytic Stability and Preferred Matrices
Detailed Elemental ProfilesChemical compatibility, stability, preparation, and atomic spectroscopic information is available by clicking an element below. For additional elements, visit our Interactive Periodic Table.
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