Acidic dissolution mechanism of natural fluorapatite. I. Milli- and microlevels of investigations

1997 ◽  
Vol 182 (1-2) ◽  
pp. 125-132 ◽  
Author(s):  
Sergey V. Dorozhkin
Author(s):  
Silvera Scaccia ◽  
Stefano Frangini

In the present paper we report the NiO solubility in a variety of alkali carbonate compositions in presence of MgO, CaCO3, BaCO3 and La2O3 additions under different conditions of gas composition and temperature. Two types of binary eutectic melts were chosen, namely the standard electrolyte (62–38) (Li-K)2CO3 and (52–48) % (Li-Na)2CO3 mixtures. The ternary eutectic melt chosen was (43.5-31.5-25.0) mol % (Li-Na-K)2CO3. The observed reduction of NiO solubility induced by the additives can be explained in terms of a higher basic character of all the modified electrolytes, although the NiO dissolution still follows an acidic dissolution mechanism in all the conditions under study.


2005 ◽  
Vol 3 (2) ◽  
pp. 208-212 ◽  
Author(s):  
Silvera Scaccia ◽  
Stefano Frangini

In the present paper we report the NiO solubility in a variety of alkali carbonate compositions in the presence of MgO, CaCO3, BaCO3, and La2O3 additions under different conditions of gas composition and temperature. Two types of binary eutectic melts were chosen, namely, the standard electrolyte (62-38) (Li-K)2CO3 and (52–48)% (Li-Na)2CO3 mixtures. The ternary eutectic melt chosen was (43.5-31.5-25.0)mol%(Li-Na-K)2CO3. The observed reduction of NiO solubility induced by the additives can be explained in terms of a higher basic character of all the modified electrolytes, although the NiO dissolution still follows an acidic dissolution mechanism in all the conditions under study.


2021 ◽  
Author(s):  
Dahiana Andrea Avila Salazar ◽  
Peter Bellstedt ◽  
Atsuhiro Miura ◽  
Yuki Oi ◽  
Toshihiro Kasuga ◽  
...  

Phosphate glass dissolution can be tailored via compositional and subsequent structural changes, which is of interest for biomedical applications such as therapeutic ion delivery. Here, solid-state 31P nuclear magnetic resonance...


1993 ◽  
Vol 92 (1-3) ◽  
pp. 97-104 ◽  
Author(s):  
F MILLAR ◽  
O CORRIGAN

2021 ◽  
pp. 014459872110287
Author(s):  
Ji Li ◽  
Wenjie Zhang ◽  
Baoli Xiang ◽  
Dan He ◽  
Shengchao Yang ◽  
...  

The reservoir in the Wuerhe Formation in the Mahu Sag, northwestern Junggar Basin, China, exhibits complex dissolution and cementation related to zeolite. The source and mechanism of diagenetic fluids are crucial in studying the reservoir genesis. Thus we investigated the key reservoirs fluids related to the zeolite and discussed their significance in the zeolite-rich reservoir of the Permian Wuerhe Formation in the Mahu Sag. Based on thin sections and electron microscope observations of rock samples and analyses of physical properties, C-O isotopes, and major elements, it is found that the reservoir underwent mainly two stages of fluid-related dissolution and cementation processes, in which the hydrocarbon-bearing fluid played the primary role in forming the high-quality reservoir. Dissolution pores are the most important storage space, and zeolite cement is the most important dissolution mineral. The geochemical characteristics of zeolite and calcite cement indicate the presence of two diagenetic fluids. The iron-rich calcite and orange-red heulandite is related to early diagenetic fluids with high iron content and higher carbon isotope values, whereas the calcites, with high manganese content and lower carbon isotope values, are formed by late acidic organic diagenetic fluids related to oil and gas activities. The hydrocarbon-bearing fluids form different spatial diagenetic zones, including the dissolution zone, buffer zone, and cementation zone, and the dissolution zone near the oil source fault is the main site of zeolite dissolution. The late fluid has the characteristics of multi-stage activity, which makes the spatial zoning expand gradually, resulting in multiple superpositions of dissolution and cementation and increasing the complexity and heterogeneity of the reservoir diagenesis. This study expands the understandings of the dissolution activities of different fluids in zeolite-rich reservoirs and also has reference significance for dissolution activity of hydrocarbon fluid in other types of reservoirs.


2021 ◽  
Author(s):  
Mohd Usman Khan ◽  
Nachiketa Rai ◽  
Mukesh Kumar Sharma

<p>As contamination in groundwater has been reported from various regions of the Indian subcontinent but no data related to heavy metal contamination of groundwater has been reported for the Bahraich area in the Indo-Gangetic plains. We report the first dataset on arsenic contamination and groundwater hydrogeochemistry, in Bahraich. This includes concentrations of heavy metal such as As, Mn, and Fe, along with major cations (Na<sup>+</sup>, K<sup>+</sup>, Ca<sup>2+</sup>and Mg<sup>2+</sup>) and anions (F<sup>-</sup>, Cl<sup>-</sup>, NO<sub>3</sub><sup>-</sup>, SO<sub>4</sub><sup>2-</sup> and PO<sub>4</sub><sup>3-</sup>), and dissolved organic carbon (DOC), along with various physico-chemical parameters such as EC, pH, and Eh from samples collected during two extensive field campaigns conducted during pre-monsoon, and post-monsoon seasons respectively. The combined use of geochemical modeling and multivariate statistical approaches such as principal component analysis (PCA) and correlation analysis (CA) suggest several processes affecting the geochemistry of groundwater including the lithological characteristics of aquifers and anthropogenic activities.</p><p>The groundwater of the study area predominantly belongs to the Ca-Mg-HCO<sub>3</sub> type hydrochemical facies. HCO<sub>3</sub><sup>−</sup>/Na<sup>+</sup> and Ca<sup>2+</sup>/Na<sup>+</sup> signatures of groundwater indicate the influence of silicate weathering and carbonate dissolution processes with the insignificant role of evaporate dissolution mechanism. As concentration was found to range from 0.6 μg/L to ~100 μg/L with almost 40% of the collected samples exceeding the WHO defined limit of 10 μg/L for drinking water. 70 % of the groundwater samples were found to have very high Fe concentrations exceeding the WHO guideline of 0.3 mg/l in drinking water. Mn concentrations in the groundwater samples were relatively low with only ~10 % of the samples exceeding the WHO defined limit for Mn (400 μg/L). The majority of the groundwater samples were found to be anoxic in nature showing low NO<sub>3</sub><sup>−</sup> & SO<sub>4</sub><sup>2-</sup> concentrations, high Fe & Mn and DOC concentrations, and negative Eh values.</p><p>Results from this study show that the reductive dissolution mechanism of iron oxyhydroxide is the dominant mechanism responsible for arsenic release in groundwater of the region, ruling out any role of sulfide oxidation and alkali desorption.</p><p> </p><p> </p>


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