Modification of calcium carbonate surface properties: macroscopic and microscopic investigations

2014 ◽  
pp. 415-428
1984 ◽  
Vol 20 (12) ◽  
pp. 1155-1158 ◽  
Author(s):  
E. Papirer ◽  
J. Schultz ◽  
C. Turchi

Geosciences ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 471 ◽  
Author(s):  
Carlos Paulo ◽  
Janice Kenney ◽  
Per Persson ◽  
Maria Dittrich

Through geological time, cyanobacterial picoplankton have impacted the global carbon cycle by sequestrating CO2 and forming authigenic carbonate minerals. Various studies have emphasized the cyanobacterial cell envelopes as nucleation sites for calcium carbonate formation. Little is known, however, about how environmental conditions (e.g., nutrient content) trigger a cell surface and its properties and, consequently, influence biomineralization. Our study aims to understand how phosphorus (P) concentration impacts the properties of cell surfaces and cell–mineral interactions. Changes to the surface properties of marine Synechococcus strains grown under various P conditions were characterized by potentiometric titrations, X-ray photoelectron spectroscopy (XPS), and tip-enhanced Raman spectroscopy (TERS). Biomineralization experiments were performed using cyanobacterial cells, which were grown under different P concentrations and exposed to solutions slightly oversaturated with respect to calcium carbonate. We observed the changes induced by different P conditions in the macromolecular composition of the cyanobacteria cell envelope and its consequences for biomineralization. The modified properties of cell surfaces were linked to carbonate precipitation rates and mineral morphology from biomineralization experiments. Our analysis shows that the increase of phosphoryl groups and surface charge, as well as the relative proportion of polysaccharides and proteins, can impact carbonate precipitation by picocyanobacteria.


2005 ◽  
Vol 486-487 ◽  
pp. 546-549 ◽  
Author(s):  
Kyung Nam Kim ◽  
Yong Do Kim

CaCO3 powders were prepared by the homogeneous precipitation method using CaCl2, urea as the starting materials. Uniform CaCO3(calcite, aragonite, vaterite) powders were obtained by various conditions. The surfaces of CaCO3 powders were modified by coating them with a lithium precursor using two different precipitation techniques: homogeneous decomposition of precipitating agents(urea, NaHCO3, NH4HCO3) and forced hydrolysis in pure water. Selecting the Ni(NO3)26H2O and urea(or NaHCO3, NH4HCO3) as Ni-source and precipitating agent respectively, the NiO could be uniformly coated on the CaCO3 powder in the aqueous system. The coating NiO layer dominated the surface properties of the coated lime powders. Calcination of these nickel hydroxide crystals in air at 500°C transformed them into NiO.


Author(s):  
Jorge Pedrosa ◽  
J.A.F. Gamelas ◽  
Ana F. Lourenço ◽  
Paulo J. Ferreira

2013 ◽  
Vol 49 (4) ◽  
pp. 1724-1733 ◽  
Author(s):  
Kazunori Kadota ◽  
Ryoichi Furukawa ◽  
Yoshiyuki Shirakawa ◽  
Atsuko Shimosaka ◽  
Jusuke Hidaka

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