ABSTRACT
The aim of this study was to characterize the riebeckite type rare earth ore found in the Bayan Obo deposit, in order to identify the distribution and occurrence of both rare earths and gangue species within the ore. Several analytical techniques were utilized to accomplish this, such as chemical analysis, quantitative XRD, a single polarizing microscope, and a mineral automatic analysis system. The analysis revealed that the primary rare earth minerals (REMs) in the ore were bastnaesite and monazite, with huanghoite, parisite, aeschynite, and fergusonite identified as secondary rare earth minerals. The main gangue species was magnetite, accompanied by smaller quantities of riebeckite and dolomite. The ore was rich in rare earth oxides, with a 3.81 wt% grade. The screen analysis of the pulverized ore indicates that the 43-100 µm fraction is the dominant size, while the finer size fractions below 43 µm contain the bastnaesite and monazite, as well as huanghoite, parisite, aeschynite, and fergusonite. Microstructural characterization showed that the REMs were both coarse-grained and fine-grained, occurring as granular aggregates and fine disseminations within the gangue. Bastnaesite and monazite were the major REMs, with dominant amounts of cerium, lanthanum, praseodymium, and neodymium, while parasite was identified as an impurity. Huanghoite and parisite contained barium and calcium as impurities, respectively. Aeschynite and fergusonite were REMs that included niobium in their composition. Bastnaesite and monazite were found to contain a much higher rare earth content than huanghoite, parisite, aeschynite, and fergusonite. Potential methods for recovering rare earths from this ore, such as magnetic separation and froth flotation, have been identified and may be applicable to similar ferruginous rare earth-bearing ores.
ABSTRACT
Boron element is widely distributed in different geologic bodies, and there are important geo-chemical applications in earth science. Halite is a common mineral found in sediment basin. However there is no good method to accurately measure the boron content in halite, which is mainly because Inductively Coupled Plasma Optical Emission Spectrometer (ICP-OES) and Inductively Coupled Plasma Mass Spectrometer (ICP-MS) are limited by the high salt matrix interference and the instrument detection limit. Thus enriching the boron element and removing the matrix interference are necessary before the measuring. In this paper, Amberlite IRA 743 boron-specific resin was applied to enrich the boron element and remove most of the high-salt matrix. The strong acid cation resin (Dowex 50 W×8, 200-400 mesh, USA) and weak-base anion resin (Ion Exchanger II, Germany) were mixed with equal volume, which could remove the foreign ions completely: meanwhile, the relative content of boron in the solution reached above 98%, and the recoveries ranged from 97.8% to 104%. 208.900 nm was chosen as the detection wavelength for ICP-OES, and the detection identification and quantification limits were 0.006 mg·L-1 and 0.02 mg·L-1, respectively. 11B was chosen as the measuring element for ICP-MS, and the detection identification and quantification limits were severally 0.036 mg·L-1 and 0.12 mg·L-1. The relative standard deviations ranged from 1.4% to 3.4% through six replicates under different salinities. Therefore, the process could be regarded as a feasible method to measure boron content in halite by ICP-OES and ICP-MS.
ABSTRACT
As a stable isotope, boron plays an important role in hydrogeology, environmental geochemistry, ore deposit geochemistry and marine paleoclimatology. However, there is no report of boron isotopic composition in gypsum. This is mainly confined to complete dissolution of Gypsum by water or acid. In this study, gypsum was converted to calcium carbonate (CaCO3) with ammonium bicarbonate(NH4HCO3) by two steps at 50°C. In every step, the mass ratio of NH4HCO3/CaSO4·2H2O was twice, and conversion rate reached more than 98%. Converted CaCO3 was totally dissolved with hydrochloric acid (the dissolution rate was over 99%). In order to overcome the difficulties of the matrix interference and the detection limit of Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES), we use Amberlite IRA 743 resin to purify and enrichment the boron at first, then eluting boron from the resin with 10mL 0.1mol/L hydrochloric acid at 75°C. The boron isotopic composition of natural gypsum samples was determined using positive thermal ionization mass spectrometry (P-TIMS). The boron isotopic composition of gypsum may be an excellent indicator for the formation environment.
