scholarly journals Ammonium carbonate gas diffusion crystallization in a continuous organic medium leads to dendritic calcium carbonate

Matters ◽  
2017 ◽  
Author(s):  
Eddie Peh ◽  
Andreas Taubert ◽  
Klaus Tauer
Nanomaterials ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 1169 ◽  
Author(s):  
Andrónico Neira-Carrillo ◽  
Patricio Vásquez-Quitral ◽  
Marianela Sánchez ◽  
Masoud Farhadi-Khouzani ◽  
Héctor Aguilar-Bolados ◽  
...  

Multiwalled carbon nanotubes (MWCNTs) are interesting high-tech nanomaterials. MWCNTs oxidized and functionalized with itaconic acid and monomethylitaconate were demonstrated to be efficient additives for controlling nucleation of calcium carbonate (CaCO3) via gas diffusion (GD) in classical as well as nonclassical crystallization, yielding aragonite and truncated calcite. For the first time, all amorphous calcium carbonate (ACC) proto-structures, such as proto calcite-ACC, proto vaterite-ACC and proto aragonite-ACC, were synthesized via prenucleation cluster (PNC) intermediates and stabilized at room temperature. The MWCNTs also showed concentration-dependent nucleation promotion and inhibition similar to biomolecules in nature. Incorporation of fluorescein-5-thiosemicarbazide (5-FTSC) dye-labeled MWCNTs into the CaCO3 lattice resulted in fluorescent hybrid nanosized CaCO3. We demonstrate that functionalized MWCNTs offer a good alternative for controlled selective crystallization and for understanding an inorganic mineralization process.


2015 ◽  
Vol 50 (4) ◽  
pp. 277-283 ◽  
Author(s):  
Jingcai Zhao ◽  
Xingfu Song ◽  
Yuzhu Sun ◽  
Bo Chen ◽  
Jianguo Yu

2010 ◽  
Vol 434-435 ◽  
pp. 597-600
Author(s):  
Xiao Hong Liang ◽  
Jun Hui Xiang ◽  
Fu Shi Zhang ◽  
Li Xing ◽  
Bo Song ◽  
...  

In this paper, the crystallization behavior of calcium carbonate between the organic-water interfaces using a slow gas-diffusion procedure is studied. The organic-water interfaces can control the crystallization of calcium carbonate to form a flower-shaped superstructure. The precipitates of calcium carbonate were identified by X-ray diffraction (XRD) and scanning electron microscopy (SEM). A possible mechanism about the self-assembly process of CaCO3 crystals has been analyzed. It is found that the morphology of CaCO3 superstructure depends on the properties of organic solvent. This paper also presents the influence of surfactant monolayer, between the biphase interfaces, on the CaCO3 superstructure. This study suggests that it is possible to control morphogenesis of calcium carbonate by a combination of a surfactant monolayer with the organic-water interfaces.


CrystEngComm ◽  
2021 ◽  
Author(s):  
Maxim Benjamin Gindele ◽  
Luisa Vanessa Steingrube ◽  
Denis Gebauer

The ammonia diffusion method (ADM) is one of the most widely used strategies for the bioinspired synthesis of minerals. Herein, we present investigations of the mineralization mechanism using an advanced...


2021 ◽  
Vol 251 ◽  
pp. 712-722
Author(s):  
Tatyana Litvinova ◽  
Ivan Oleynik

Treatment of apatite raw materials is associated with the formation of large-tonnage waste – phosphogypsum. The content of rare earth metals in such waste reaches 1 %, which makes it possible to consider it a technogenic source for obtaining rare earth metals and their compounds. Up to the present moment, there are neither processing plants, nor an efficient process flow to handle phosphogypsum dumps. It is rational to use a way that involves extraction of valuable components and overall reduction of phosphogypsum dumps. Such process flow is available with carbonate conversion of phosphogypsum to alkali metal or ammonium sulfate and calcium carbonate upon the condition of associated extraction of rare earth metal (REM) compounds. Associated extraction of REM compounds becomes possible since they form strong and stable complexes with hard bases according to Pearson, which among other things include carbonate, phosphate and sulfate anions. Formation of lanthanide complexes with inorganic oxygen-containing anions is facilitated by the formation of high-energy Ln-O bonds. The study focuses on the dissolution of lanthanide phosphates in carbonate media. It was established that formation of REM carbonate complexes from their phosphates is a spontaneous endothermic process and that formation of lanthanide carbonates and hydroxides serves as thermodynamic limitation of dissolution. A shift in equilibrium towards the formation of carbonate complexes is achieved by increasing the temperature to 90-100 °C and providing an excess of carbonate. The limiting stage of REM phosphate dissolution in carbonate media is external diffusion. This is indicated by increasing rate of the process with an intensification of stirring, first order of the reaction and the value of activation energy for phosphate dissolution from 27 to 60 kJ/mol. A combination of physical and chemical parameters of the process allowed to develop an engineering solution for associated REM extraction during carbonate conversion of phosphogypsum, which included a 4-5 h conversion of phosphogypsum at temperature of 90-110 °C by an alkali metal or ammonium carbonate solution with a concentration of 2-3 mol/l. As a result, a solution with alkali metal (ammonium) sulfate is obtained, which contains REMs in the form of carbonate complexes and calcium carbonate. The rate of REM extraction into the solution reaches no less than 93 %. Rare earth metals are separated from the mother liquor by precipitation or sorption on anion exchange resins, while the excess of alkali metal or ammonium carbonate is returned to the start of the process.


Sign in / Sign up

Export Citation Format

Share Document