scholarly journals Biomineral Reactivity: The Kinetics of the Replacement Reaction of Biological Aragonite to Apatite

Minerals ◽  
2018 ◽  
Vol 8 (8) ◽  
pp. 315 ◽  
Author(s):  
Martina Greiner ◽  
Lurdes Férnandez-Díaz ◽  
Erika Griesshaber ◽  
Moritz Zenkert ◽  
Xiaofei Yin ◽  
...  

We present results of bioaragonite to apatite conversion in bivalve, coral and cuttlebone skeletons, biological hard materials distinguished by specific microstructures, skeletal densities, original porosities and biopolymer contents. The most profound conversion occurs in the cuttlebone of the cephalopod Sepia officinalis, the least effect is observed for the nacreous shell portion of the bivalve Hyriopsis cumingii. The shell of the bivalve Arctica islandica consists of cross-lamellar aragonite, is dense at its innermost and porous at the seaward pointing shell layers. Increased porosity facilitates infiltration of the reaction fluid and renders large surface areas for the dissolution of aragonite and conversion to apatite. Skeletal microstructures of the coral Porites sp. and prismatic H. cumingii allow considerable conversion to apatite. Even though the surface area in Porites sp. is significantly larger in comparison to that of prismatic H. cumingii, the coral skeleton consists of clusters of dense, acicular aragonite. Conversion in the latter is sluggish at first as most apatite precipitates only onto its surface area. However, the process is accelerated when, in addition, fluids enter the hard tissue at centers of calcification. The prismatic shell portion of H. cumingii is readily transformed to apatite as we find here an increased porosity between prisms as well as within the membranes encasing the prisms. In conclusion, we observe distinct differences in bioaragonite to apatite conversion rates and kinetics depending on the feasibility of the reaction fluid to access aragonite crystallites. The latter is dependent on the content of biopolymers within the hard tissue, their feasibility to be decomposed, the extent of newly formed mineral surface area and the specific biogenic ultra- and microstructures.

1949 ◽  
Vol 27b (4) ◽  
pp. 353-360
Author(s):  
C. A. Winkler ◽  
A. T. Hutcheon

A commercial type cathode ray oscillograph has been used in conjunction with three stages of direct current amplification to give suitable voltage amplification in the range 0.001 to 1 v. The effect of traces of grease in diminishing the measured surface area of silver amalgam has been observed. Curves are shown for the determination of cadmium surface areas and rate of increase of cadmium polarization.


1997 ◽  
Vol 17 (3) ◽  
pp. 295-300 ◽  
Author(s):  
Malgorzata Kuzlan ◽  
Krzysztof Pawlaczyk ◽  
Katarzyna Wieczorowska Tobis ◽  
Katarzyna Korybalska ◽  
Andrzej Breborowicz ◽  
...  

Objective Evaluation of peritoneal surface area and its permeability during dialysis in rats of various ages. Design Study I: planimetry of peritoneum and its topographic areas was performed in 47 rats of various ages (8 -30 weeks). Study II: net ultrafiltration (UF), dialysate-to-serum ratios for urea, creatinine, albumin, and total protein as well as their peritoneal permeability coefficients, were measured during a 1-hour peritoneal exchange with Dianeal 2.5%, in 21 rats of different ages (9 30 weeks) and with various peritoneal surface areas. Animals: Male Wistar rats. Results The peritoneal surface area in rats increases during aging, but young animals with lower body weight have a relatively larger peritoneal surface area than older, larger animals. The area of the topographic fragments of peritoneum expressed as a percentage of the total peritoneal surface is steady during aging. Efficiency of transperitoneal water removal expressed as net UF per amount of absorbed glucose declines in older animals, with larger peritoneal surface areas. Dialysate/serum ratio of solutes transported from blood to dialysate is proportional to peritoneal surface area. Permeability coefficient (K) of peritoneum to urea and creatinine is unchanged during the aging of animals. However peritoneal permeability (K) to albumin increases during aging, with the opposite tendency for total proteins. Conclusions Kinetics of peritoneal dialysis in rats of different ages is determined by peritoneal surface area and permeability of peritoneum to individual solutes.


2009 ◽  
Vol 41 (3) ◽  
pp. 267-274 ◽  
Author(s):  
N. Djordjevic ◽  
S. Martinovic ◽  
M. Vlahovic ◽  
P. Jovanic ◽  
V. Vidojkovic ◽  
...  

During sintering of the 2MgO-2Al2O3-5SiO2 system, cordierite, an attractive ceramic material because of its properties, is obtained. Effects of mechanochemical activation of stoichiometric mixtures, performed to investigate possibilities of lowering cordierite formation temperature during sintering, were monitored by thermogravimetric and differential thermal analyses. Specific surface areas of the mechanically activated powder mixtures were determined by the BET method. Kinetics of the specific surface area increase was analyzed using the Boltzmann model. It was confirmed that with activation time increase, temperatures of phase transformations were shifted to lower values and, according to FTIR analysis no significant changes occurred during material aging. According to the obtained results, it may be concluded that since mechanochemical activation has an influence on the treated powder mixture, lowering of the cordierite formation temperature during the sintering process is expected.


Author(s):  
M. Marko ◽  
A. Leith ◽  
D. Parsons

The use of serial sections and computer-based 3-D reconstruction techniques affords an opportunity not only to visualize the shape and distribution of the structures being studied, but also to determine their volumes and surface areas. Up until now, this has been done using serial ultrathin sections.The serial-section approach differs from the stereo logical methods of Weibel in that it is based on the Information from a set of single, complete cells (or organelles) rather than on a random 2-dimensional sampling of a population of cells. Because of this, it can more easily provide absolute values of volume and surface area, especially for highly-complex structures. It also allows study of individual variation among the cells, and study of structures which occur only infrequently.We have developed a system for 3-D reconstruction of objects from stereo-pair electron micrographs of thick specimens.


1992 ◽  
Vol 57 (11) ◽  
pp. 2302-2308
Author(s):  
Karel Mocek ◽  
Erich Lippert ◽  
Emerich Erdös

The kinetics of the reaction of solid sodium carbonate with sulfur dioxide depends on the microstructure of the solid, which in turn is affected by the way and conditions of its preparation. The active form, analogous to that obtained by thermal decomposition of NaHCO3, emerges from the dehydration of Na2CO3 . 10 H2O in a vacuum or its weathering in air at room temperature. The two active forms are porous and have approximately the same specific surface area. Partial hydration of the active Na2CO3 in air at room temperature followed by thermal dehydration does not bring about a significant decrease in reactivity. On the other hand, if the preparation of anhydrous Na2CO3 involves, partly or completely, the liquid phase, the reactivity of the product is substantially lower.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jeongpil Kim ◽  
Jeong-Hyun Eum ◽  
Junhyeok Kang ◽  
Ohchan Kwon ◽  
Hansung Kim ◽  
...  

AbstractHerein, we introduce a simple method to prepare hierarchical graphene with a tunable pore structure by activating graphene oxide (GO) with a two-step thermal annealing process. First, GO was treated at 600 °C by rapid thermal annealing in air, followed by subsequent thermal annealing in N2. The prepared graphene powder comprised abundant slit nanopores and micropores, showing a large specific surface area of 653.2 m2/g with a microporous surface area of 367.2 m2/g under optimized conditions. The pore structure was easily tunable by controlling the oxidation degree of GO and by the second annealing process. When the graphene powder was used as the supercapacitor electrode, a specific capacitance of 372.1 F/g was achieved at 0.5 A/g in 1 M H2SO4 electrolyte, which is a significantly enhanced value compared to that obtained using activated carbon and commercial reduced GO. The performance of the supercapacitor was highly stable, showing 103.8% retention of specific capacitance after 10,000 cycles at 10 A/g. The influence of pore structure on the supercapacitor performance was systematically investigated by varying the ratio of micro- and external surface areas of graphene.


Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 446
Author(s):  
Miriam González-Castaño ◽  
Estelle le Saché ◽  
Cameron Berry ◽  
Laura Pastor-Pérez ◽  
Harvey Arellano-García ◽  
...  

This work establishes the primordial role played by the support’s nature when aimed at the constitution of Ni2P active phases for supported catalysts. Thus, carbon dioxide reforming of methane was studied over three novel Ni2P catalysts supported on Al2O3, CeO2 and SiO2-Al2O3 oxides. The catalytic performance, shown by the catalysts’ series, decreased according to the sequence: Ni2P/Al2O3 > Ni2P/CeO2 > Ni2P/SiO2-Al2O3. The depleted CO2 conversion rates discerned for the Ni2P/SiO2-Al2O3 sample were associated to the high sintering rates, large amounts of coke deposits and lower fractions of Ni2P constituted in the catalyst surface. The strong deactivation issues found for the Ni2P/CeO2 catalyst, which also exhibited small amounts of Ni2P species, were majorly associated to Ni oxidation issues. Along with lower surface areas, oxidation reactions might also affect the catalytic behaviour exhibited by the Ni2P/CeO2 sample. With the highest conversion rate and optimal stabilities, the excellent performance depicted by the Ni2P/Al2O3 catalyst was mostly related to the noticeable larger fractions of Ni2P species established.


2021 ◽  
Vol 129 (1) ◽  
Author(s):  
Serge Kräutle ◽  
Jan Hodai ◽  
Peter Knabner

AbstractWe consider a macroscale model of transport and reaction of chemical species in a porous medium with a special focus on mineral precipitation–dissolution processes. In the literature, it is frequently proposed that the reaction rate should depend on the reactive mineral surface area, and so on the amount of mineral. We point out that a frequently used model is ill posed in the sense that it admits non-unique solutions. We investigate what consequences this non-uniqueness has on the numerical solution of the model. The main novelty in this article is our proposal of a certain substitution which removes the ill-posedness from the system and which leads to better numerical results than some “ad hoc methods.” We think that the proposed substitution is a rather elegant way to get rid of the non-uniqueness and the numerical difficulties and is much less technical than other ideas. As a proof of concept, we present some numerical tests and simulations for the new model.


2021 ◽  
Author(s):  
Atal Ahmadzai

Alerted by increasing water insecurity and energy demand, countries, mainly in the Global South, are building dams of unprecedented magnitude. Hundreds of large dams (≥ 100 metres) have been constructed since 2000, with hundreds more under construction. Analyses of the physical attributes of these dams present a concerning image. While they create expansive reservoirs with large surface areas, they have inefficient surface area-to-volume ratios ('S2VR'). Their unprecedented size and the reservoirs’ expansive surface area, indicate severe environmental costs, mainly through ecological disturbances to the (riverine) aquatic ecosystems; and greenhouse gas emissions (GHG). Other ecological costs due to the larger S2VR include a high evaporation rate and compromised biodiversity of a wider area, both up- and downstream. The safety and environmental aspects of these large dams should be robustly scrutinised.


Author(s):  
Hieр Nguyen Tien

The kinetics of metallic cobalt nanopowder synthesizing by hydrogen reduction from Co(OH)2 nanopowder under isothermal conditions were studied. Co(OH)2 nanopowder was prepared in advance by chemical deposition from aqueous solutions of Co(NO3)2 cobalt nitrate (10 wt.%) and NaOH alkali (10 wt.%) at room temperature, pH = 9 under continuous stirring. The hydrogen reduction of Co(OH)2 nanopowder under isothermal conditions was carried out in a tube furnace in the temperature range from 270 to 310 °C. The crystal structure and composition of powders was studied by X-ray phase analysis. The specific surface area of samples was measured using the BET method by low-temperature nitrogen adsorption. The average particle size of powders was determined by the measured specific surface area. Particles size characteristics and morphology were investigated by transmission and scanning electron microscopes. Kinetic parameters of Co(OH)2 hydrogen reduction under isothermal conditions were calculated using the Gray–Weddington model and Arrhenius equation. It was found that the rate constant of reduction at t = 310 °C is approximately 1.93 times higher than at 270 °C, so the process accelerates by 1.58 times for 40 min of reduction. The activation energy of cobalt nanopowder synthesizing from Co(OH)2 by hydrogen reduction is ~40 kJ/mol, which indicates a mixed reaction mode. It was shown that cobalt nanoparticles obtained by the hydrogen reduction of its hydroxide at 280 °C are aggregates of equiaxed particles up to 100 nm in size where individual particles are connected to several neighboring particles by contact isthmuses.


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