The concentrations of the rare earth elements (REE) in surface waters and sediments, when normalized on an element-by-element basis to one of several rock standards and plotted versus atomic number, yield curves that ...The concentrations of the rare earth elements (REE) in surface waters and sediments, when normalized on an element-by-element basis to one of several rock standards and plotted versus atomic number, yield curves that reveal their partitioning between different sediment fractions and the sources of those fractions, for example, between terrestrial-derived lithogenous debris and seawater-derived biogenous detritus and hydrogenous metal oxides. The REE of ancient sediments support their partitioning into these same fractions and further contribute to the identification of the redox geochemistry of the sea water in which the sediments accumulated. The normalized curves of the REE that have been examined in several South American wine varietals can be interpreted to reflect the lithology of the bedrock on which the vines may have been grown, suggesting limited fractionation during soil development.展开更多
Vertisol developed on argillaceous rocks has its special pedogenic processes and properties, and formed some secondary nodules. In study area, contents of rare earth elements (REE) are significantly different in diffe...Vertisol developed on argillaceous rocks has its special pedogenic processes and properties, and formed some secondary nodules. In study area, contents of rare earth elements (REE) are significantly different in different sedimentary rocks due to varied contents of clay fraction and clay mineral composition, etc. Under the dry and hot climate, REEs were less differentiated than their parent sedimentary rocks. However, REEs in secondary nodules formed in pedogenic process display their specific behaviors. They are more concentrated in iron concretions, the content of heavy REEs increases relatively, and positive Ce-anomaly appears. But, negative Ce-anomaly was found in calcium concretions, while normal Ce content in parent rocks and vertisol.展开更多
This work presents an investigation of solvent extraction parameters in order to obtain high purity cerium from a mixture containing other rare earths elements, as an alternative to oxidation and selective precipitati...This work presents an investigation of solvent extraction parameters in order to obtain high purity cerium from a mixture containing other rare earths elements, as an alternative to oxidation and selective precipitation or dissolution. The study was carried out using a sample of sulfuric liquor obtained from the leaching of monazite rich in light rare earth elements (La, Ce, Pr, Nd) provided by INB (Indústrias Nucleares do Brasil S.A.). Experiments were carried out in chloridric, nitric and sulfuric media. The nitric and hydrochloric solutions were prepared by precipitation of the REE from the sulfuric liquor as rare earths oxalate, calcining the precipitate and dissolving it with nitric or hydrochloric acid. The separation of cerium was investigated in its trivalent and tetravalent forms. The parameters investigated were: type and concentration of extractant, type and amount of the oxidizing agent, liquor acidity, and volumetric ratio between organic and aqueous phases. The preference of the organic phase to extract cerium in its oxidized form (IV) over the other rare earths elements was confirmed, allowing the obtainment of a high purity cerium solution. The best results were achieved in nitric medium, with cerium in its tetravalent form, using cationic extractants (P507 or D2EHPA) and a mixture of potassium persulfate and silver chloride as oxidizing agents, yielding over 99% of cerium extraction with over 99% of purity.展开更多
文摘The concentrations of the rare earth elements (REE) in surface waters and sediments, when normalized on an element-by-element basis to one of several rock standards and plotted versus atomic number, yield curves that reveal their partitioning between different sediment fractions and the sources of those fractions, for example, between terrestrial-derived lithogenous debris and seawater-derived biogenous detritus and hydrogenous metal oxides. The REE of ancient sediments support their partitioning into these same fractions and further contribute to the identification of the redox geochemistry of the sea water in which the sediments accumulated. The normalized curves of the REE that have been examined in several South American wine varietals can be interpreted to reflect the lithology of the bedrock on which the vines may have been grown, suggesting limited fractionation during soil development.
文摘Vertisol developed on argillaceous rocks has its special pedogenic processes and properties, and formed some secondary nodules. In study area, contents of rare earth elements (REE) are significantly different in different sedimentary rocks due to varied contents of clay fraction and clay mineral composition, etc. Under the dry and hot climate, REEs were less differentiated than their parent sedimentary rocks. However, REEs in secondary nodules formed in pedogenic process display their specific behaviors. They are more concentrated in iron concretions, the content of heavy REEs increases relatively, and positive Ce-anomaly appears. But, negative Ce-anomaly was found in calcium concretions, while normal Ce content in parent rocks and vertisol.
文摘This work presents an investigation of solvent extraction parameters in order to obtain high purity cerium from a mixture containing other rare earths elements, as an alternative to oxidation and selective precipitation or dissolution. The study was carried out using a sample of sulfuric liquor obtained from the leaching of monazite rich in light rare earth elements (La, Ce, Pr, Nd) provided by INB (Indústrias Nucleares do Brasil S.A.). Experiments were carried out in chloridric, nitric and sulfuric media. The nitric and hydrochloric solutions were prepared by precipitation of the REE from the sulfuric liquor as rare earths oxalate, calcining the precipitate and dissolving it with nitric or hydrochloric acid. The separation of cerium was investigated in its trivalent and tetravalent forms. The parameters investigated were: type and concentration of extractant, type and amount of the oxidizing agent, liquor acidity, and volumetric ratio between organic and aqueous phases. The preference of the organic phase to extract cerium in its oxidized form (IV) over the other rare earths elements was confirmed, allowing the obtainment of a high purity cerium solution. The best results were achieved in nitric medium, with cerium in its tetravalent form, using cationic extractants (P507 or D2EHPA) and a mixture of potassium persulfate and silver chloride as oxidizing agents, yielding over 99% of cerium extraction with over 99% of purity.
