Urea hydrolysis and inorganic N in a Luvisol after application of fertiliser containing rare-earth elements

Soil Research ◽  
2003 ◽  
Vol 41 (4) ◽  
pp. 741 ◽  
Author(s):  
Xingkai Xu ◽  
Zijian Wang ◽  
Yuesi Wang ◽  
Kazuyuki Inubushi

In recent decades, Chinese agriculturists have used rare-earth-containing fertilisers as basal fertilisers together with N fertilisers (e.g. urea). We studied urea hydrolysis and its hydrolysis products in a laboratory experiment using urea-N fertiliser with rare earths at rates from 0.5 to 50% (w/w). The results indicated that application of rare earths at a high rate could result in a short-term inhibition of urea hydrolysis and an increase in soil (NH4+ + NO3– + NO2–)-N content. When the application rate of rare earths was higher than 5% of the applied urea-N (corresponding to 10 mg/kg soil), soil exchangeable NH4+-N content increased significantly following the hydrolysis of the applied urea. Increasing the application rate of rare earths appeared to reduce the content of soil urea-derived (NO3– + NO2–)-N. A substantial reduction in soil pH was found immediately after application of rare earths and urea. We conclude that application of rare earths at >10 mg/kg may lead to a substantial increase in the content of urea-derived N in the soil, via the inhibition of urea hydrolysis and nitrification.

Significance Short-term factors combined to strengthen prices, including widespread flooding in China’s Sichuan province and low capacity utilisation among producers outside China. In the first two months of 2021, Chinese exports of rare earths rebounded by 28.8% year-on-year to 7,068 tonnes, although this was boosted by the low base of a demand slump in early 2020. Impacts Beijing has threatened to cut off supplies of refined rare earth products to US aerospace firm Lockheed Martin for trading with Taiwan. Norway may plan mining after finding polymetallic sulfides in its seabed containing high concentrations of lithium and certain rare earths. China also imports rare earths, and problems with shipping raw materials from Myanmar will exacerbate its rare earth shortages. US firm Energy Fuels is partnering with Neo Performance’s European operations to provide concentrates free of radioactive materials.


Minerals ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 952
Author(s):  
Youming Yang ◽  
Xiaolin Zhang ◽  
Kaizhong Li ◽  
Li Wang ◽  
Fei Niu ◽  
...  

Rare earths dissolved in carbonate solutions exhibit a metastable state. During the period of metastability, rare earths dissolve stably without precipitation. In this paper, neodymium was chosen as a representative rare earth element. The effects of additional NaCl and CO2 on the metastable state were investigated. The metastable state can be controlled by adding NaCl to the Na2CO3 solution. Molecular dynamics studies indicated that the Cl− provided by the additional NaCl partially occupied the coordination layer of Nd3+, causing the delayed formation of neodymium carbonate precipitation. In addition, the additional NaCl decreased the concentration of free carbonate in the solution, thereby reducing the behavior of free contact between carbonate and Nd, as well as resulting in the delay of Nd precipitate formation. Consequently, the period of the metastable state was prolonged in the case of introduction of NaCl. However, changing the solution environment by introducing CO2 can destroy the metastable state rapidly. Introduction of CO2 gas significantly decreased the CO32− content in the solution and increased its activity, resulting in an increase of the free CO32− concentration of the solution in the opposite direction. As a result, the precipitation process was accelerated and the metastable state was destroyed. It was possible to obtain a large amount of rare earth carbonate precipitation in a short term by introducing CO2 into the solution with dissolved rare earths in the metastable state to achieve rapid separation of rare earths without introducing other precipitants during the process.


2015 ◽  
Vol 816 ◽  
pp. 9-14 ◽  
Author(s):  
Yan Li ◽  
Mei Hui Song ◽  
Qian Yu ◽  
Xiao Chen Zhang

In this article, the high-performance modified AlN powder was prepared, using Y(NO3)3·6H2O as the modifying agent, and characterizing by pH meter, TG , XRD and SEM. The results show that the Y2O3 coating was formed on the AlN surface, the pH value of aluminum nitride of treatment suspension solution maintains 7.75 in water bath for 100 hours. Therefore the conclusion is that surface modification with rare earths can effectively inhibit the hydrolysis of the AlN powder.


2020 ◽  
Vol 05 ◽  
Author(s):  
Silas Santos ◽  
Orlando Rodrigues ◽  
Letícia Campos

Background: Innovation mission in materials science requires new approaches to form functional materials, wherein the concept of its formation begins in nano/micro scale. Rare earth oxides with general form (RE2O3; RE from La to Lu, including Sc and Y) exhibit particular proprieties, being used in a vast field of applications with high technological content since agriculture to astronomy. Despite of their applicability, there is a lack of studies on surface chemistry of rare earth oxides. Zeta potential determination provides key parameters to form smart materials by controlling interparticle forces, as well as their evolution during processing. This paper reports a study on zeta potential with emphasis for rare earth oxide nanoparticles. A brief overview on rare earths, as well as zeta potential, including sample preparation, measurement parameters, and the most common mistakes during this evaluation are reported. Methods: A brief overview on rare earths, including zeta potential, and interparticle forces are presented. A practical study on zeta potential of rare earth oxides - RE2O3 (RE as Y, Dy, Tm, Eu, and Ce) in aqueous media is reported. Moreover, sample preparation, measurement parameters, and common mistakes during this evaluation are discussed. Results: Potential zeta values depend on particle characteristics such as size, shape, density, and surface area. Besides, preparation of samples which involves electrolyte concentration and time for homogenization of suspensions are extremely valuable to get suitable results. Conclusion: Zeta potential evaluation provides key parameters to produce smart materials seeing that interparticle forces can be controlled. Even though zeta potential characterization is mature, investigations on rare earth oxides are very scarce. Therefore, this innovative paper is a valuable contribution on this field.


Author(s):  
Sophia Kalantzakos

In 2010, because of a geopolitical incident between China and Japan, seventeen elements of the periodic table known as rare earths became notorious overnight. An “unofficial” and temporary embargo of rare-earth shipments to Japan alerted the world to China’s near monopoly position on the production and export of these indispensable elements for high-tech, defense, and renewable energy sources. A few months before the geopolitical confrontation, China had chosen to substantially cut export quotas of rare earths. Both events sent shockwaves across the markets, and rare-earth prices skyrocketed, prompting reactions from industrial nations and industry itself. The rare-earth crisis is not a simple trade dispute, however. It also raises questions about China’s use of economic statecraft and the impacts of growing resource competition. A detailed and nuanced examination of the rare-earth crisis provides a significant and distinctive case study of resource competition and its spill-over geopolitical effects. It sheds light on the formulation, deployment, longevity, effectiveness, and, perhaps, shortsightedness of policy responses by other industrial nations, while also providing an example of how China might choose to employ instruments of economic statecraft in its rise to superpower status.


2021 ◽  
Vol 141 (3) ◽  
pp. 527-533
Author(s):  
P. Moog ◽  
M. Dozan ◽  
J. Betzl ◽  
I. Sukhova ◽  
H. Kükrek ◽  
...  

Abstract Introduction Although the WALANT technique’s long-term safeness has been demonstrated in many studies, there are only few data investigating its short-term effects on tissue perfusion and oxygen levels. It was hypothesized that, temporarily, critical levels of tissue perfusion may occur. Methods Seventeen patients, who were scheduled for different procedures in WALANT technique, were injected with 5–7 ml of 1% Articain containing 1:200,000 epinephrine at the finger base. Capillary-venous oxygen saturation, hemoglobin volume in the capillaries, and relative blood flow in the fingertips were recorded once per second by white light spectrometry and laser Doppler flowmetry before, during and after injection for an average of 32 min. Results Clinically, no persistent tissue malperfusion was observed, and there were no postoperative complications. Capillary-venous oxygen saturation was reduced by ≥ 30% in seven patients. Critical levels of oxygen saturation were detected in four patients during 13 intervals, each lasting for 132.5 s on average. Oxygen saturation returned to noncritical values in all patients by the end of the observation period. Blood flow in the fingertips was reduced by more than 30% in nine patients, but no critical levels were observed, as with the hemoglobin. Three patients demonstrated a reactive increase in blood flow of more than 30% after injection. Conclusions Injection of tumescent local anesthesia containing epinephrine into finger base may temporarily cause a substantial reduction in blood flow and lead to critical levels of oxygen saturation in the fingertips. However, this was fully reversible within minutes and does not cause long-term complications.


Minerals ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 20
Author(s):  
Deniz Talan ◽  
Qingqing Huang

The increasing industrial demand for rare earths requires new or alternative sources to be found. Within this context, there have been studies validating the technical feasibility of coal and coal byproducts as alternative sources for rare earth elements. Nonetheless, radioactive materials, such as thorium and uranium, are frequently seen in the rare earths’ mineralization, and causes environmental and health concerns. Consequently, there exists an urgent need to remove these radionuclides in order to produce high purity rare earths to diversify the supply chain, as well as maintain an environmentally-favorable extraction process for the surroundings. In this study, an experimental design was generated to examine the effect of zeolite particle size, feed solution pH, zeolite amount, and contact time of solid and aqueous phases on the removal of thorium and uranium from the solution. The best separation performance was achieved using 2.50 g of 12-µm zeolite sample at a pH value of 3 with a contact time of 2 h. Under these conditions, the adsorption recovery of rare earths, thorium, and uranium into the solid phase was found to be 20.43 wt%, 99.20 wt%, and 89.60 wt%, respectively. The Freundlich adsorption isotherm was determined to be the best-fit model, and the adsorption mechanism of rare earths and thorium was identified as multilayer physisorption. Further, the separation efficiency was assessed using the response surface methodology based on the development of a statistically significant model.


2011 ◽  
Vol 98 (3-4) ◽  
pp. 125-131 ◽  
Author(s):  
Tian Jun ◽  
Yin Jingqun ◽  
Chen kaihong ◽  
Rao Guohua ◽  
Jiang Mintao ◽  
...  

2014 ◽  
Vol 1010-1012 ◽  
pp. 928-933
Author(s):  
Ju Chi Kuang ◽  
Xiao Gang Chen ◽  
Min Hua Chen

The principle and methodology of effluent treatment by iron-carbon micro electrolysis were introduced in the paper. Then design of the orthogonal experiments for dyeing effluent treatment was formulated. Discussion of influences of related factors on effluent treatment followed. Results were got after the detailed analysis. Therefore, we deduced the mechanism that the cations of Transition Metal (TM) and rare earth (RE) assist of zero-valent irons catalyzing degradation of dyeing effluent. The mechanism is formed based on the following explanation. Cations of manganese and cobalt easily penetrate Fe0lattices, while Ce4+cations do it difficultly because of their larger radius. Thus Ce4+is weaker than both of Mn2+and Co2+for helping zero-valent irons to improve their activity. Furthermore, because the valence electron structure of Mn2+is more stable than that of Co2+, Mn2+is better for assisting zero-valent iron catalysis of degradation of dyeing effluent than Co2+. Therefore, ranking of influence for zero-valent iron catalysis activity from greatest to smallest is Mn2+, Co2+and Ce4+.


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