Optimization and modeling of boric acid extraction from colemanite in water saturated with carbon dioxide and sulphur dioxide gases

In this study, the boric acid extraction from colemanite ore in aqueous media saturated by CO₂ and SO₂ gases was studied and the effects of relevant parameters, namely; reaction temperature, solid-to-liquid ratio, mean particle size, stirring speed and reaction time have been investigated on the boric acid extraction from colemanite ore by using the fractional factorial design and central composite design methods. The chosen experimental parameter levels were as follows: reaction temperature, 11.4–58.6 °C; solid-to-liquid ratio, 0.0685–0.1315 g/mL; mean particle size, 0.2835–3 mm; stirring speed, 107–893 rpm; reaction time, 7.125–22.875 min. A model has been developed between the boric acid extraction efficiency from colemanite ore and relevant parameters by means of variance analysis by using the matlab computer software and the obtained model was used to determine optimum conditions. The optimum conditions were found to be as follows: reaction temperature, 41 °C; solid-to-liquid ratio, 0.0685 g/mL; mean particle size, 0.2835 mm; stirring speed, 266 rpm; reaction time, 7 min. The calculated boric acid extraction efficiency from colemanite ore was approximately 99.9% under the optimum conditions.     

Impact of Alkaline Earth Metals on Aqueous Speciation of Uranium(VI) and Sorption on Quartz

The effect of Mg-, Ca-, and Sr–Uranyl-Carbonato complexes with respect to sorption on quartz was studied by means of batch experiments with U(VI) concentration of 0.126 × 10⁻⁶ M in the presence and absence of Mg, Ca, and Sr (each 1 mM) at pH from 6.5 to 9. In the absence of alkaline earth elements, 90% of the U(VI) sorbed on the quartz surface at all pH. In the presence of Mg, Ca, and Sr, the sorption of U(VI) on quartz decreased to 50, 10, and 30%, respectively. Sorption kinetics of U(VI) on quartz is faster in the absence of alkaline earth elements and reached equilibrium after 12 h, whereas in the presence of Mg, Ca and Sr, the kinetics of U(VI) sorption on quartz is pH dependent and attained equilibrium after 24 h. Aqueous speciation calculations for alkaline earth uranyl carbonates were carried out by using PHREEQC with the Nuclear Energy Agency thermodynamic database (NEA_2007) by adding constants for MUO₂(CO₃)₃²⁻ and M₂UO₂(CO₃)₃⁰ (M = Ca, Mg, Sr). This study reveals that alkaline earth elements can have a significant effect on the aqueous speciation of U(VI) under neutral to alkaline pH conditions and subsequently sorption behavior and mobility of U(VI) in aqueous environments.     

Extraction of uranium from heap leach liquor with tri-n-octylamine: Equilibrium data and flow-sheet calculations

The recovery of uranium from an acid heap leach liquor has been investigated. Tertiary amines (tri-n-octylamine) have been chosen as extractants because of their high selectivity and efficiency. According to the theory of the mechanism of extraction by amines, an equation has been proposed for the extraction isotherms of uranium. In amine extraction systems the organic-aqueous volume ratio is more important for uranium extraction efficiency than amine concentration. Equilibrium data are further developed according to the McCabe-Thiele approach to calculate from extraction isotherms and stripping isotherms the number of theoretical stages. Three stages and two stages respectively are predicted for extraction and stripping circuits with an over-all uranium recovery of 98.9%.     

Heat-induced changes in speciation and extraction of uranium associated with sheet silicate minerals

Three samples of gouge from a U-mineralised fault, and two model samples, montmorillonite and muscovite, spiked with U, were heat-treated at a range of temperatures up to 1100 °C. Mineralogical changes were followed by thermal analysis, powder XRD and electron microscopy, and U extractability was measured by extraction with NH₄⁺. Changes in U speciation in the montmorillonite sample were followed using EXAFS spectroscopy. On heating, the minerals progressively dehydrate, dehydroxylate and eventually decompose to form new phases in a glassy matrix. In the case of montmorillonite (90% of U extractable from unheated material), U extractability increased slightly on heating to temperatures around 400 °C. Almost 50% of U was extracted from unheated muscovite, and this increased slightly by 450 °C. Above 500–600 °C, U extractability from both montmorillonite and muscovite declined to very low levels, reflecting dehydration of the uranyl ion and trapping in the new phases and glassy matrix. Uranium extractability from the natural samples was much lower in all cases (0.25–5% of the total before heating). In 2 samples, a significant increase in U extraction was associated with dehydroxylation at around 600 °C, followed by a decrease to very low levels at higher temperatures. Uranium extraction from the third natural sample, which contained X-ray amorphous U minerals, decreased steadily on heating. The results show that changes in U extraction can be related to structural and morphological changes in sheet silicate minerals. Heat treatment has potential to fix U but only if temperatures above 800 °C are reached. If only lower temperatures, in the range 400–600 °C, are used, then U extraction may increase.     

Geochemistry of mafic rocks of the Karakaya complex,Turkey: evidence for plume-involvement in the Palaeotethyan extensional regime during the Middle and Late Triassic

The Karakaya Complex within the Early Mesozoic Cimmerian Orogeny in northern Turkey represents the remnants of the Palaeotethys. It includes slivers and/or mega-blocks of slightly metamorphic basic volcanic rocks associated with fossiliferous sediments as well as hypabyssal and intrusive rocks with basaltic-andesitic to ultramafic compositions. They display two distinct compositional groups; namely alkaline and variably tholeiitic. The alkaline basalt samples are more akin to oceanic-island basalts (OIB) with relatively enriched trace element characteristics together with strong partitioning in HREE ([La/Yb]_N = 5.8–16.2), suggesting that garnet is present as a residual phase in the source of those basalts. The variably tholeiitic samples apart from diabases display E-MORB characteristics; being relatively depleted compared to the alkaline counterparts and less fractionated REE patterns ([La/Yb]_N = 2.1–3.6). The diabases, on the other hand, are distinctively different with a significant negative Nb anomaly (Zr/Nb = 28.9–43.4) and flat REE patterns ([La/Yb]_N = 0.8–1.4), suggesting their generation above a supra-subduction zone, probably a back-arc basin. These results may suggest that a mantle plume-related magmatism associated with extensional oceanic system should have been installed within Palaeotethys during Middle-Late Triassic time, which was then incorporated into subduction–accretion prism forming the final picture, that is, “the Karakaya Complex”.     

Calcic amphiboles in calc-alkaline and alkaline magmas: thermobarometric and chemometric empirical equations valid up to 1,130°C and 2.2 GPa

The following article presents constraints of the stability of Mg-rich (Mg/(Mg + Fe²⁺) > 0.5) calcic amphibole in both calc-alkaline and alkaline magmas, testing of previous thermobarometers, and formulation of new empirical equations that take into consideration a large amount of literature data (e.g. more than one thousand amphibole compositions among experimental and natural crystals). Particular care has been taken in choosing a large number of natural amphiboles and selecting quality experimental data from literature. The final database of experimental data, composed of 61 amphiboles synthesized in the ranges of 800–1,130°C and 130–2,200 MPa, indicates that amphibole crystallization occurs in a horn-like P–T stability field limited by two increasing curves (i.e. the thermal stability and an upper limit), which should start to bend back to higher pressures. Among calcic amphiboles, magnesiohornblendes and tschermakitic pargasites are only found in equilibrium with calc-alkaline melts and crystallize at relatively shallow conditions (P up to ~1 GPa). Kaersutite and pargasite are species almost exclusively found in alkaline igneous products, while magnesiohastingsite is equally distributed in calc-alkaline and alkaline rocks. The reliability of previous amphibole applications was checked using the selected experimental database. The results of this testing indicate that none of the previous thermobarometers can be successfully used to estimate the P, T and fO₂ in a wide range of amphibole crystallization conditions. Multivariate least-square analyses of experimental amphibole compositions and physico-chemical parameters allowed us to achieve a new thermobarometric model that gives reasonably low uncertainties (T ± 23.5°C, P ± 11.5%, H₂O_melt ± 0.78wt%) for calc-alkaline and alkaline magmas in a wide range of P–T conditions (up to 1,130°C and 2,200 MPa) and ∆NNO values (±0.37 log units) up to 500 MPa. The ^AK-^[4]Al relation in amphibole can be readily used to distinguish crystals of calc-alkaline liquids from those of alkaline magmas. In addition, several chemometric equations allowing to estimate the anhydrous composition of the melts in equilibrium with amphiboles of calc-alkaline magmas were derived.     

Late Triassic alkaline complex in the Sulu UHP terrane: Implications for post-collisional magmatism and subsequent fractional crystallization

Continental subduction and its interaction with overlying mantle wedge are recognized as fundamental solid earth processes, yet the dynamics of this system remains ambiguous. In order to get an insight into crust–mantle interaction triggered by partial melting of subudcted continental crust during its exhumation, we carried out a combined study of the Shidao alkaline complex from the Sulu ultrahigh pressure (UHP) terrane. The alkaline complex is composed of shoshonitic to ultrapotassic (K₂O: 3.4–9.3 wt.%) gabbro, pyroxene syenite, amphibole syenite, quartz syenite, and granite. Field studies suggest that the mafic rocks are earlier than the felsic ones in sequence. LA-ICPMS zircon U–Pb dating on them gives Late Triassic ages of 214 ± 2 to 200 ± 3 Ma from mafic to felsic rocks. These ages are slightly younger than the Late Triassic ages (225–210 Ma) of the felsic melts from partial melting of the Sulu UHP terrane during exhumation. The alkaline rocks have wide ranges of SiO₂ (49.7–76.7 wt.%), MgO (8.25–0.03 wt.%), Ni (126.0–0.07 ppm), and Cr (182.0–0.45 ppm) contents. The contents of MgO, total Fe₂O₃, CaO, TiO₂ and P₂O₅ decrease with increasing SiO₂ contents. The contents of Na₂O, K₂O, and Al₂O₃ increase from gabbro to amphibole syenite, and decrease from amphibole syenite to granite, respectively. The alkaline rocks have characteristics of an arc-like pattern in trace element distribution, e.g., enrichment of LREE, LILE (Rb and Ba), Th and U, depletion of HFSE (Nb, Ta, P and Ti), and positive Pb anomalies. From the mafic rocks to the felsic rocks, the (La/Yb)_N ratios and the contents of the total REE, Sr and Ba decrease but the Rb contents increase. The alkaline rocks with high SiO₂ contents also display features of an A2-type granitoids, e.g., high contents of total alkalis, Zr and Nb and high ratios of Fe₂O₃^T/MgO, Ga/Al, Yb/Ta and Y/Nb, suggesting a post-collisional magmatism during exhumation of the Sulu UHP terrane. The alkaline rocks have homogeneous initial ⁸⁷Sr/⁸⁶Sr ratios (0.7058–0.7093) and negative ε_Nd(t) values (− 18.6 to − 15.0) for whole-rock. The Sr–Nd isotopic data remain almost unchanged with varying SiO₂ and MgO contents, suggesting a fractional crystallization (FC) process from the same parental magma. Our studies suggest a crust–mantle interaction in continental subduction interface as follows: (1) hydrous felsic melts from partial melting of subducted continental crust during its exhumation metasomatized the overlying mantle wedge to form a K-rich and amphibole-bearing mantle; (2) partial melting of the enriched lithospheric mantle generated the Late Triassic alkaline complex under a post-collisional setting; and (3) the alkaline magma experienced subsequent fractionational crystallization mainly dominated by olivine, clinopyroxene, plagioclase and alkali feldspar.     

Efficient flotation recovery of lead and zinc from refractory lead-zinc ores under low alkaline conditions

In this study, a new flotation approach, a low-alkaline and non-desliming process, was introduced for improving lead and zinc recoveries, lowering production cost and reducing environmental pollution. Lab-scale experiments results show that the new process contributed to the flotation of the complex mixed sulfide-oxide lead and zinc ore regarding two aspects: (1) High alkaline process (pH = 12±) was replaced by low alkaline process (pH = 9±) by using collector WS (a mixture of ethyl thiocarbamate, ammonium dibutyldithiophosphate and dithiophosphate-25) and combined depressant Na₂S/ZnSO₄/Na₂SO₃ for lead sulfide flotation; (2) Non-desliming process was successfully achieved by using collector MA (a mixture of ether amine, hydroxyethyl cellulose and polyacrylic acid) and combined depressant SHP/SS (sodium hexametaphosphate/sodium silicate) for zinc oxide flotation. And 43.37% Pb in the Pb concentrate was recovered, the corresponding Pb grade was 52.73%, total 84.42% Zn was recovered by the flotation of zinc sulfide minerals and zinc oxide minerals. Moreover, the two aspects of the new approach were systematically verified from lab-scale to industrial-scale application. The industrial-scale flotation tests show that Pb recovery in Pb concentrate increased by 1.86% compared with that of original system during industrial-scale tests period, and the Pb recovery increased by 4.09% compared with that of original system before industrial-scale tests period, while the Zn operating recovery in zinc oxide concentrate improved by 19.52%. Moreover, the total reagent cost of the whole new process significantly declined by 3.93 yuan per ton of ore.     

The applicability of accelerated solvent extraction (ASE) to extract lipid biomarkers from soils

We investigated the ability of accelerated solvent extraction (ASE) to extract selected lipid biomarkers (C₁₉–C₃₄ n-alkanes, n-alcohols and n-fatty acids as well as dehydroabietic acid and β-sitosterol) from a sandy soil profile under Corsican pine. Two organic layers (moss and F1) as well as two mineral soil horizons (EA and C1) were sampled and extracted with DCM/MeOH (93:7 v/v) by ASE at 75 °C and a pressure of 6.9 × 10⁶ Pa or 17 × 10⁶ Pa. Soxhlet extractions were used as the established reference method. After clean-up and derivatization with BSTFA, the extracts were analyzed on GC/MS.Using Soxhlet as a reference, we found ASE to extract all compounds adequately. The n-alkanes, especially, were found to be extracted very efficiently from all horizons studied. Only the n-fatty acids and β-sitosterol from the organic layers seemed to be extracted at a slightly lower efficiency by ASE. In all but two instances the relative abundance of extracted lipids within a component class was the same regardless of the extraction method used.Using a higher pressure in the ASE extractions significantly increased the extraction efficiency for all component classes in the moss layer, except β-sitosterol. The effect was most pronounced for the n-alkanes. In the EA horizon, a higher pressure slightly reduced the extraction efficiency for dehydroabietic acid. The observed differences between ASE and Soxhlet extractions as well as the pressure effect can be explained by a decrease in polarity of the extractant due to the elevated pressure and temperature applied during ASE extractions as compared to Soxhlet extractions. This would mainly increase the extraction efficiency of the least polar biomarkers: the n-alkanes as was observed. In addition, a better penetration of still partially water-filled micro pores under elevated pressure and temperature may have played a role.     

Investigations on the extraction of molybdenum and vanadium from ammonia leaching residue of spent catalyst

Extraction of molybdenum and vanadium from ammonia leaching residue (main chemical composition: 2.05% Mo, 0.42% V, 65.6% Al₂O₃ and 10.7% SiO₂) of spent catalyst was investigated by roasting the residue with soda carbonate, followed by hydrometallurgical treatment of the roasted products. In the roasting process, over 91.3% of molybdenum and 90.1% of vanadium could be extracted when a charge containing a sodium carbonate to spent catalyst ratio of 0.15 was roasted at 750 °C for 45 min and the roasted mass was leached with water (liquid to solid ratio of 2) at 80–90 °C for 15 min. After the purification of leach liquor, an extraction solvent consisting of 20 vol.% trialkylamine (N₂₃₅, commercialized in China) and 10 vol.% secondary octyl alcohol (phase modifier) dissolved in sulfonated kerosene was used to extract molybdenum and vanadium in leach liquor. 10 wt.% ammonia water was used as stripping agent. Adding 30 g/l NH₄NO₃ to the stripping solution and adjusting the pH to 7–8.5, over 99% of vanadium can be crystallized as ammonium metavanadate. Over 98% of molybdenum can be crystallized as ammonium polymolybdate when pH is between 1.5 and 2.5 (pH is adjusted by HNO₃). Ammonium metavanadate and ammonium polymolybdate were calcinated at 500–550 °C, the purity of MoO₃ and V₂O₅ was 99.08% and 98.06% respectively. In the whole process, 88.2% of molybdenum and 87.1% of vanadium could be achieved. The proposed roasting, leaching and separation steps give a feasible alternative for the processing of ammonia leaching residue of spent catalyst and can be applied in the comprehensive utilization of low grade molybdenum ores.     

Impact of fertilizer phosphorus application on phosphorus release kinetics in some calcareous soils

Phosphate reactions and retention in the soil are of paramount importance from the perspective of plant nutrition and fertilizer use efficiency. The objective of this work was to study the kinetics of phosphorus (P) desorption in different soils of Hamadan in fertilized and unfertilized soils. Soils were fertilized with 200 mg P kg⁻¹. Fertilized and unfertilized soils were incubated at 25 ± 1°C for 6 months. After that, release of P was studied by successive extraction with 0.5 M NaHCO₃ over a period of 1,752 h. The results showed that phosphorus desorption from the fertilized and unfertilized soils began with a fast initial reaction, followed by a slow secondary reaction. The amount of P released after 1,752 h in fertilized and unfertilized soils ranged from 457 to 762.4 and 309.6 to 586.7 mg kg⁻¹, respectively. The kinetics of cumulative P release was evaluated using the five kinetic equations. Phosphorus desorption kinetics were best described by parabolic diffusion law, first order, and power function equations. Rate constants of these equations were higher in fertilized than unfertilized soils. Results from this study indicate that release rate of P plays a significant role in supplying available P and released P in runoff.     

Genetic link between saline and carbonatitic mantle fluids: The system NaCl-CaCO3-MgCO3 ± H2O ± Fe0 at 6 GPa

Melt inclusions in kimberlitic minerals and diamonds indicate that chlorides are important constituents of mantle carbonatite melts. Besides, alkaline chlorides are important constituents of saline high-density fluids (HDFs) found in diamonds from kimberlites and placers around the world. Continuous compositional variations suggest that saline and carbonatitic HDFs could be genetically linked. However, the essence of this link remains unclear owing to the lack of data on phase relations in the chloride-carbonate systems under pressure. Here we studied subsolidus and melting phase relations in the system NaCl–CaCO₃–MgCO₃ at 6 GPa and 1000–1600 °C using a Kawai-type multianvil press. We found that at 1000 °C, subsolidus assemblage consists of halite, magnesite, and aragonite. At higher temperatures, the stabilization of dolomite splits the subsolidus area into two partial ternary fields: halite + magnesite + dolomite and halite + dolomite + aragonite. The minimum on the liquidus surface corresponds to the halite-dolomite-aragonite ternary eutectic, situated at 1100 °C. The eutectic melt has Ca# 89 and contains 30 wt.% NaCl (26 mol% 2NaCl). The system has two ternary peritectics: halite + dolomite = magnesite + liquid located near the ternary eutectic and magnesite + dolomite = Mg-dolomite + liquid situated between 1300 and 1400 °C. Although under dry conditions incipient melting yields carbonate-dominated melt, the addition of water facilitates the fusion of NaCl and expands the liquid field to NaCl-rich compositions with up to 70 wt.% NaCl. The obtained results favor the idea that hydrous saline melts/fluids (brines) found as inclusions in diamonds could be a lower temperature derivative of mantle carbonatite melts and disagree with the hypothesis on chloride melt generation owing to the chloride-carbonate liquid immiscibility since no such immiscibility was established. We also studied the interaction of the NaCl–CaCO₃–MgCO₃ system with iron metal and found that carbonate reduction produces C-bearing species (Fe⁰, Fe-C melt, Fe₃C, Fe₇C₃, C⁰) and wüstite containing Na₂O, CaO, and MgO. Besides, a carbonate chloride compound, Ca₂Cl₂CO₃, was established among the reaction products. The interaction between NaCl-bearing carbonate melt shifts its composition toward Mg-poor and NaCl-rich. Given the above, an alternative hypothesis can be proposed, according to which the interaction of alkaline chloride-bearing carbonate melts formed in the subduction zones with the reduced mantle should be accompanied by diamond crystallization and shift the composition of the melt from carbonatitic to alkali-rich saline.     

CO<Subscript>2</Subscript> absorption by alkaline soils and its implication to the global carbon cycle

Motivated by the rapid increase in atmospheric CO₂ due to human activities since the Industrial Revolution, and the climate changes it produced, the world’s concerned scientific community has made a huge effort to investigate the global carbon cycle. However, the results reveal that the global CO₂ budget cannot be balanced, unless a “missing sink” is invoked. Although numerous studies claimed to find the “missing sink”, none of those claims has been widely accepted. This current study showed that alkaline soil on land are absorbing CO₂ at a rate of 0.3–3.0 μmol m⁻² s⁻¹ with an inorganic, non-biological process. The intensity of this CO₂ absorption is determined by the salinity, alkalinity, temperature and water content of the saline/alkaline soils, which are widely distributed on land. Further studies revealed that high salinity or alkalinity positively affected the CO₂ absorbing intensity, while high temperature and water content had a negative effect on the CO₂ absorbing intensity of these soils. This inorganic, non-biological process of CO₂ absorption by alkaline soils might have significant implications to the global carbon budget accounting.     

白云鄂博矿床钍富集过程及空间分布规律

白云鄂博矿床为一特大型Fe-REE多金属矿床,同时伴生有巨量的钍资源。然而,目前开发利用的矿种主要是铁和稀土资源,钍资源利用率几乎为零。查明矿床中钍资源的赋存状态和分布规律及揭示钍资源的富集过程及机制是今后钍资源开发利用的重要基础。本文依托近些年的系统采样及分析测试成果,对白云鄂博主、东、西矿区570个样品进行了详细的矿物学观察和全岩化学分析,在不同类型矿石中识别出以硅钍石为主的独立含钍矿物,硅钍石除少量呈现被稀土矿物包裹现象外,通常以细脉状穿插于稀土矿物内部,显示其明显滞后富集的特点。矿区Th O_-2平均品位达0.0322%,高出地壳钍克拉克值(9.6×10^-6)30多倍,各种矿石类型中Th O₂含量具有明显的差别,在云母型、闪石型、霓石型和萤石型矿石中具有高含量Th O₂,而白云石型矿石中Th O₂含量较低,指示矿区钍矿化主要形成于碱性热液交代和萤石化阶段。此外矿区随深度增加钍矿化作用加强,显示出矿床具有良好的钍资源成矿潜力。     

Element fractionation by sequential extraction in a soil with high carbonate content

The influence of carbonate and other buffering substances in soils on the results of a 3-step sequential extraction procedure (BCR) used for metal fractionation was investigated. Deviating from the original extraction scheme, where the extracts are analysed only for a limited number of metals, almost all elements in the soils were quantified by X-ray fluorescence spectroscopy, in the initial samples as well as in the residues of all extraction steps. Additionally, the mineral contents were determined by X-ray diffractometry. Using this methodology, it was possible to correlate changes in soil composition caused by the extraction procedure with the release of elements. Furthermore, the pH values of all extracts were monitored, and certain extraction steps were repeated until no significant pH-rise occurred. A soil with high dolomite content (27%) and a carbonate free soil were extracted. Applying the original BCR-sequence to the calcareous soil, carbonate was found in the residues of the first two steps and extract pH-values rose by around two units in the first and second step, caused mainly by carbonate dissolution. This led to wrong assignment of the carbonate elements Ca, Mg, Sr, Ba, and also to decreased desorption and increased re-adsorption of ions in those steps. After repetition of the acetic acid step until extract pH remained low, the carbonate was completely destroyed and the distributions of the elements Ca, Mg, Sr, Ba as well as those of Co, Ni, Cu, Zn and Pb were found to be quite different to those determined in the original extraction. Furthermore, it could be shown that the effectiveness of the reduction process in step two was reduced by increasing pH: Fe oxides were not significantly attacked by the repeated acetic acid treatments, but a 10-fold amount of Fe was mobilized by hydroxylamine hydrochloride after complete carbonate destruction. On the other hand, only small amounts of Fe were released anyway. Even repeated reduction steps did not destroy the amorphous Fe oxides completely, showing that 0.1 mol L⁻¹ hydroxylamine hydrochloride was not strong enough to attack these oxides effectively.The extraction sequences were carried out not only on the soil samples, but also on their coarse and fine fractions (> or <2 μm). The fine fraction of the calcareous soil contained only 10% dolomite, but was enriched in organic matter and clay minerals, which also resulted in increased extract pH-values during the sequential extraction. Hence, the effects on ion release in the fine fraction were similar to those of the whole soil. Since the destruction of the organic matter was incomplete after regular oxidation, the H₂O₂-treatment of the fine fraction had to be repeated. The addition of the extractable amounts of the two fractions showed good agreement to the results obtained for extraction of the whole soils. Likewise the pH-values of the carbonate-free soil extracts did not increase significantly, therefore it was concluded that repetitions of extraction steps for this soil were not necessary.Extract-pHs should always be controlled so that extraction conditions are comparable; to be able to use the BCR extraction scheme or similar ones for carbonate- and organic-rich samples this is mandatory. Single extraction steps should be repeated if pH rises too much; additionally the oxidizing step should be performed more than twice for samples rich in organic substances, depending upon the violence of the reaction with H₂O₂. If these precautions are neglected the validity of the extraction data is likely to be questionable.     

A greenstone belt in southeast Tibet: An accreted middle–late Permian oceanic plateau

Studies of accreted oceanic plateau sections provide crucial information on their structures, compositions, and origins. We investigate the petrogenesis of ultramafic–mafic rocks in the Tangjia–Sumdo greenstone belt of southeast Tibet using petrography, whole-rock geochemistry, and U-Pb zircon geochronology. These rocks are divided into four groups based on geochemical characteristics that include depleted and tholeiitic mafic rocks, transitional mafic rocks, enriched and alkaline mafic rocks, and picritic ultramafic rocks. Depleted and tholeiitic mafic rocks have the oldest crystallization ages (～272 Ma), followed by picritic ultramafic rocks (～270 Ma), transitional mafic rocks (267–254 Ma), and enriched and alkaline mafic rocks (252–250 Ma). Hafnium and neodymium isotope ratios of depleted and tholeiitic mafic rocks (ε_Hf(t) = +13.1–+16.9; ε_Nd(t) = +6.9–+7.1), transitional mafic rocks (ε_Hf(t) = +1.8–+16.9; ε_Nd(t) = +0.8–+5.5), enriched and alkaline mafic rocks (ε_Hf(t) = +0.5–+5.4; ε_Nd(t) = ?1.5 to +1.9) and picritic ultramafic rocks (ε_Hf(t) = +14.9–+17.2; ε_Nd(t) = +7.8–+9.0) are similar to those of N-MORB, E-MORB, OIB and depleted-type picritic mafic rocks in other oceanic plateaus, respectively. The geochemical characteristics of the depleted and tholeiitic mafic rocks suggest that they formed by partial melting of depleted spinel lherzolite in a mid-ocean ridge setting, whereas the picritic ultramafic rocks suggest a high degree of partial melting of depleted lherzolite in a hot mantle plume head. The transitional mafic rocks formed by partial melting of moderately enriched garnet lherzolite. The youngest rocks (enriched and alkaline mafic rocks) formed by partial melting of a more enriched garnet lherzolite (compared to transitional mafic rocks) at relatively low temperatures. We propose that the depleted and tholeiitic mafic rocks represent normal oceanic crust of the Sumdo Paleo-Tethys Ocean and the transitional mafic rocks, enriched and alkaline mafic rocks and picritic ultramafic rocks are the fragments of the oceanic plateau, which were related to middle–late Permian mantle plume activity in the Sumdo Paleo-Tethys Ocean. We further suggest that the majority of the Tangjia–Sumdo greenstone belt represents a middle–late Permian oceanic plateau that reflects a previously unrecognized middle–late Permian mantle plume.     

Experimental design approach to the optimisation of hydrocarbons extraction from the sediment: Method development and application

Extraction and analysis of organic pollutants from matrices such as sediment constitute an essential step in environmental research. However, the extraction for quantitative analysis can turn out to be difficult because these compounds are present in trace levels and can be strongly bound to the sorbent matrix. Consequently, accuracy of environmental analyses mainly depends on the efficiency and the robustness of the extraction step. In this work, a sequential ASE extraction procedure was applied to the extraction of polycyclic aromatic and aliphatic hydrocarbons (PAHs, Me-PAHs and n-alkanes) in sediment samples. The extraction protocol was developed for 26 PAHs, including the 16 PAHs of the United-States Environmental Protection Agency (EPA) priority list, for 17 alkylated PAHs homologues and for 29 n-alkanes (from n-C₁₂ to n-C₄₀). A set of 30 experiments was carried out for the determination of the optimal extraction conditions. The four parameters studied were pressure, temperature, extraction time and nature of the solvent. Extracts were analyzed by gas chromatography (GC-MS and GC-FID) after clean-up and concentration. The optimal extraction conditions selected for pressure, temperature, extraction time and nature of solvent were respectively 14 MPa, 160 °C, 24 min and hexane/acetone (1/1 v/v). The analytical procedure was validated by comparing predicted and experimental values of sediment samples and by analyzing standard reference material. The validated method was then applied to establish a depth profile contamination in the sediment of the Deûle River in Northern France.     

Kinetics of Au (III) extraction by DBC from hydrochloric solution using Lewis cell

The kinetics of forward extraction [AuCl₄]^? from aqua regia medium by diethylene glycol dibutyl ether (DBC) have been investigated by the Lewis cell (LC) technique. At first gold extraction has been carried out under different experimental conditions for achieving the stoichiometry coefficients and the value of the extraction equilibrium constant (K = 0.1). For kinetic data treatment, flux ‘F’ method has been applied. Reaction order with respect to DBC, pH and [AuCl₄]^? was determined and then the rate constant was calculated. The rate of gold extraction from 2 M chloride medium can be expressed as F = 10^0.88[AuCl₄^?]^1.25 [DBC]^0.4 [H⁺]^?0.22. Kinetics data were treated by EVIEWS software and coefficients were obtained. The comparison of manual and software results indicated that the results had good conformity. Influence of temperature was studied and then activation energy, E_a, (11.17 kJ/mol), activation enthalpy (11.66 kJ/mol) and entropy (?187 J/mol K) were calculated by using Arrhenius and activation complex theory respectively. E_a value (< 20.9 kJ/mol) indicates that, the extraction of gold (III) in the investigated system is controlled by diffusion process.     

Measurement of the Isotopic Composition of Molybdenum in Geological Samples by MC‐ICP‐MS using a Novel Chromatographic Extraction Technique

A novel preconcentration method is presented for the determination of Mo isotope ratios by multi‐collector inductively coupled plasma‐mass spectrometry (MC‐ICP‐MS) in geological samples. The method is based on the separation of Mo by extraction chromatography using N‐benzoyl‐N‐phenylhydroxylamine (BPHA) supported on a microporous acrylic ester polymeric resin (Amberlite CG‐71). By optimising the procedure, Mo could be simply and effectively separated from virtually all matrix elements with a single pass through a small volume of BPHA resin (0.5 ml). This technique for separation and enrichment of Mo is characterised by high selectivity, column efficiency and recovery (~ 100%), and low total procedural blank (~ 0.18 ng). A ¹⁰⁰Mo‐⁹⁷Mo double spike was mixed with samples before digestion and column separation, which enabled natural mass‐dependent isotopic fractionation to be determined with a measurement reproducibility of  < 0.09‰ (δ^98/95Mo, 2s) by MC‐ICP‐MS. The mean δ^98/95Mo_{SRM 3134} (NIST SRM 3134 Mo reference material; Lot No. 891307) composition of the IAPSO seawater reference material measured in this study was 2.00 ± 0.03‰ (2s, n = 3), which is consistent with previously published values. The described procedure facilitated efficient and rapid Mo isotopic determination in various types of geological samples.