scholarly journals An Exceptionally Stable and Widespread Hydrated Amorphous Calcium Carbonate Precipitated By the Dog Vomit Slime Mold Fuligo Septica (Myxogastria)

Author(s):  
Laurence A.J. Garvie ◽  
Péter Németh ◽  
László Trif

Abstract Biogenic amorphous calcium carbonate (ACC) is typically metastable and can rapidly transform through aging, dehydration, and/or heating to crystalline calcium carbonate. Gaining insight into its structure and properties is typically hampered by its tendency to crystallize over short time periods once isolated from the host organism, and also by the small quantities that are usually available for study. Here, we describe an exceptionally stable hydrated ACC (HACC) precipitated by the cosmopolitan slime mold, Fuligo septica (L.) F.H. Wigg. (1780). A single slime mold can precipitate up to one gram of HACC over the course of one night. Powder x-ray diffraction (XRD) patterns, transmission electron microscopy (TEM) images, infrared absorption (IR) spectra, and lack of optical birefringence are consistent with an amorphous material. XRD simulations supported by thermogravimetric (TG) and evolved gas analysis (EGA) data suggest an intimate association of organic matter with ~1-nm-sized ACC units that have monohydrocalcite- and calcite-like nano-structural properties. It is postulated that this association imparts the extreme stability of the HACC by preventing loss of H2O and subsequent crystallization. The composition, structure, and thermal behavior of the HACC precipitated by F. septica collected over 8000 km apart, and in markedly different environments, suggests a common structure, as well as similar biochemical and biomineralization mechanisms for the HACC formation.

1999 ◽  
Vol 14 (5) ◽  
pp. 2138-2146 ◽  
Author(s):  
Eric L. Brosha ◽  
John Davey ◽  
Fernando H. Garzon ◽  
Shimshon Gottesfeld

The dehydrogenation of C60 · H18.7 was studied using thermogravimetric and powder x-ray diffraction analysis. C60 · H18.7 was found to be stable up to 430 °C in Ar at which point the release of hydrogen initiated the collapse of a fraction of fullerene molecules. X-ray diffraction analysis performed on C60 · H18.7 samples dehydrogenated at 454, 475, and 600 °C displayed an increasing volume fraction of amorphous material. The decomposition product comprises randomly oriented, single-layer graphite sheets. Evolved gas analysis using gas chromatograph (GC) mass spectroscopy confirmed the presence of both H2 and methane upon dehydrogenation. Attempts to improve reversibility or reduce hydrogenation/ dehydrogenation temperatures by addition of Ru and Pt catalysts were unsuccessful.


Minerals ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 270 ◽  
Author(s):  
Ayaka Saito ◽  
Hiroyuki Kagi ◽  
Shiho Marugata ◽  
Kazuki Komatsu ◽  
Daisuke Enomoto ◽  
...  

Calcite is a ubiquitous mineral in nature. Heavy alkaline-earth elements with large ionic radii such as Sr2+ and Ba2+ are highly incompatible to calcite. Our previous study clarified that incompatible Sr2+ ions can be structurally incorporated into calcite through crystallization from amorphous calcium carbonate (ACC). In this study, we synthesized Sr-doped calcite with Sr/(Sr + Ca) up to 30.7 ± 0.6 mol% and Ba-doped calcite with Ba/(Ba + Ca) up to 68.6 ± 1.8 mol%. The obtained Ba-doped calcite samples with Ba concentration higher than Ca can be interpreted as Ca-containing barium carbonates with the calcite structure which have not existed so far because barium carbonate takes the aragonite structure. X-ray diffraction (XRD) patterns of the Sr-doped and Ba-doped calcite samples obtained at room temperature showed that reflection 113 gradually weakened with increasing Sr/(Sr + Ca) or Ba/(Ba + Ca) ratios. The reflection 113 disappeared at Ba/(Ba + Ca) higher than 26.8 ± 1.6 mol%. Extinction of reflection 113 was reported for pure calcite at temperatures higher than 1240 K, which was attributed to the rotational (dynamic) disorder of CO32− in calcite. Our Molecular Dynamics (MD) simulation on Ba-doped calcite clarified that the CO32− ions in Ba-doped calcites are in the static disorder at room temperature. The CO32− ions are notable tilted and displaced from the equilibrium position of pure calcite.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Michika Sawada ◽  
Kandi Sridhar ◽  
Yasuharu Kanda ◽  
Shinya Yamanaka

AbstractWe report a synthesis strategy for pure hydroxyapatite (HAp) using an amorphous calcium carbonate (ACC) colloid as the starting source. Room-temperature phosphorylation and subsequent calcination produce pure HAp via intermediate amorphous calcium phosphate (ACP). The pre-calcined sample undergoes a competitive transformation from ACC to ACP and crystalline calcium carbonate. The water content, ACC concentration, Ca/P molar ratio, and pH during the phosphorylation reaction play crucial roles in the final phase of the crystalline phosphate compound. Pure HAp is formed after ACP is transformed from ACC at a low concentration (1 wt%) of ACC colloid (1.71 < Ca/P < 1.88), whereas Ca/P = 1.51 leads to pure β-tricalcium phosphate. The ACP phases are precursors for calcium phosphate compounds and may determine the final crystalline phase.


Author(s):  
Jako S. Eensalu ◽  
Kaia Tõnsuaadu ◽  
Jasper Adamson ◽  
Ilona Oja Acik ◽  
Malle Krunks

AbstractThermal decomposition of tris(O-ethyldithiocarbonato)-antimony(III) (1), a precursor for Sb2S3 thin films synthesized from an acidified aqueous solution of SbCl3 and KS2COCH2CH3, was monitored by simultaneous thermogravimetry, differential thermal analysis and evolved gas analysis via mass spectroscopy (TG/DTA-EGA-MS) measurements in dynamic Ar, and synthetic air atmospheres. 1 was identified by Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR) measurements, and quantified by NMR and elemental analysis. Solid intermediates and final decomposition products of 1 prepared in both atmospheres were determined by X-ray diffraction (XRD), Raman spectroscopy, and FTIR. 1 is a complex compound, where Sb is coordinated by three ethyldithiocarbonate ligands via the S atoms. The thermal degradation of 1 in Ar consists of three mass loss steps, and four mass loss steps in synthetic air. The total mass losses are 100% at 800 °C in Ar, and 66.8% at 600 °C in synthetic air, where the final product is Sb2O4. 1 melts at 85 °C, and decomposes at 90–170 °C into mainly Sb2S3, as confirmed by Raman, and an impurity phase consisting mostly of CSO 2 2− ligands. The solid-phase mineralizes fully at ≈240 °C, which permits Sb2S3 to crystallize at around 250 °C in both atmospheres. The gaseous species evolved include CS2, C2H5OH, CO, CO2, COS, H2O, SO2, and minor quantities of C2H5SH, (C2H5)2S, (C2H5)2O, and (S2COCH2CH3)2. The thermal decomposition mechanism of 1 is described with chemical reactions based on EGA-MS and solid intermediate decomposition product analysis.


2020 ◽  
Vol 22 (4) ◽  
pp. 1900922 ◽  
Author(s):  
Christoph Lauer ◽  
Sebastian Haußmann ◽  
Patrick Schmidt ◽  
Carolin Fischer ◽  
Doreen Rapp ◽  
...  

1980 ◽  
Vol 53 (3) ◽  
pp. 437-511 ◽  
Author(s):  
D. W. Brazier

Abstract An attempt has been made to review the development of thermoanalytical procedures as they have been applied to elastomers and elastomer systems over the past 10 years. For all rubber industry products, temperature and its effects, either alone or in conjunction with the chemical environment, play an important role from the production stage through to the final failure of the product in the field. It is thus not surprising that thermal analysis, in which temperature is the prime variable, has found such diverse applications in elastomer studies. The identification and quantitative analysis of rubber formulations have received most attention. Such formulations produce characteristic “fingerprints” when studied in DTA, DSC, TG, or TMA. In DSC, the determination of the glass transition characteristics, the observation and determination of crystallinity, the detection of cyclization reactions, and the monitoring of thermal and oxidative degradation characteristics can all be observed in a single experiment covering the temperature range from −150 to +600°C. At normal heating rates, e.g., 20°C/min, such information is available in 40 min. TG/DTG analysis can yield the elastomer or elastomers content, oil and plasticizer, carbon black (level and often type), and inorganic ash in less than 60 min. Processing and curing can also be studied. Blend compatibility can be assessed on the basis of both Tg and crystallinity measurements and the data used to determine optimum mixing times. Sulfur vulcanization and peroxide curing of elastomers is readily monitored by DSC and can be used for confirmation analysis of the presence of curatives. Limitations in such analysis exist, but as understanding and ability to interpret cure exotherms increase, valuable information about the mechanism and the nature of the cured network will be obtained. The testing of rubber compounds involves many hours of labor by current procedures. The rapidity of thermal analysis promises to offer some relief. In addition to DSC and TG, TMA, a relatively new technique, offers a rapid approach to low-temperature testing. Dynamic mechanical analysis (DMA) offers a rapid route to determining dynamic properties, but as yet, relatively little has been published on the application of this new technique to elastomers. As environmental concern increases, techniques such as evolved gas analysis (EGA) and combined techniques such as TG/gas chromatography are predicted to play an important role. As for the future, it is readily apparent that the principles of the methods have been established and, in several cases, it now remains to reduce them to a practical level. In some areas, such as vulcanization studies, much remains to be undertaken to improve our interpretive skills. Although there is some indication that certain industries have produced “in-house” standards for the analysis of rubber compounds by DSC and TG/DTG, it will only be when national and international standards organizations study and produce standard procedures, that the techniques will be generally adopted. Maurer's prediction in 1969 of increased applications of DTA and TG in elastomer studies has undoubtedly proved correct, and with the proliferation of reliable commercial instrumentation, significant developments can be anticipated in the next decade.


2006 ◽  
Vol 118 ◽  
pp. 661-665 ◽  
Author(s):  
Dae Hwan Kwon ◽  
Thuy Dang Nguyen ◽  
Pyuck Pa Choi ◽  
Ji Soon Kim ◽  
Young Soon Kwon

The microstructure and properties of Cu-TiB2 composites produced by high-energy ball-milling of TiB2 powders and spark-plasma sintering (SPS) were investigated. TiB2 powders were mechanically milled at a rotation speed of 1000rpm for short time in Ar atmosphere, using a planetary ball mill. To produce Cu-xTiB2 composites( x = 2.5, 5, 7.5 and 10wt.% ), the raw and milled TiB2 powders were mixed with Cu powders by means of a turbular mixer, respectively. Sintering of mixed powders was carried out in a SPS facility under vacuum. High-energy ball-milling resulted in refinement of TiB2 particles. XRD patterns of milled TiB2 powders indicated broader TiB2 peaks with decreased intensities. After sintering at 950 for 5min using the raw and milled TiB2 mixture powders, the sintered density decreased with increasing TiB2 content regardless of milling of TiB2. In the case of raw TiB2, hardness rapidly increased from 4 to 44 HRB with increasing TiB2 content. The electrical conductivity changed from 95.5 to 80.7 %IACS. For mixtures of Cu powders with milled TiB2 powders, hardness increased from 38 to 67 HRB as TiB2 content increased, while the electrical conductivity varied from 88% to 51 % IACS. When compared to compacts sintered with raw and milled TiB2 powders, the electrical conductivity of specimens with raw TiB2 powder was higher than that of specimens with milled TiB2 powder, while hardness was slightly lower.


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