2014
DOI: 10.1155/2014/985185
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Characterization and Thermal Dehydration Kinetics of Highly Crystalline Mcallisterite, Synthesized at Low Temperatures

Abstract: The hydrothermal synthesis of a mcallisterite (Mg2(B6O7(OH)6)2·9(H2O)) mineral at low temperatures was characterized. For this purpose, several reaction temperatures (0–70°C) and reaction times (30–240 min) were studied. Synthesized minerals were subjected to X-ray diffraction (XRD), fourier transform infrared (FT-IR), and Raman spectroscopies and scanning electron microscopy (SEM). Additionally, experimental analyses of boron trioxide (B2O3) content and reaction yields were performed. Furthermore, thermal gra… Show more

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Cited by 11 publications
(4 citation statements)
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“…"Asymmetric stretching of B (4) -O" can be explained with the peaks in the range of 1200-950 cm À1 . The peaks at the lower wavelength values of 750 cm À1 can be interpreted with the "bending of B (3) -O" [6][7][8]. In Raman analyses of magnesium borates, the characteristic peaks are seen in the wavelength region of 1200-250 cm À1 .…”
Section: Magnesium Borate Mineralsmentioning
confidence: 99%
See 1 more Smart Citation
“…"Asymmetric stretching of B (4) -O" can be explained with the peaks in the range of 1200-950 cm À1 . The peaks at the lower wavelength values of 750 cm À1 can be interpreted with the "bending of B (3) -O" [6][7][8]. In Raman analyses of magnesium borates, the characteristic peaks are seen in the wavelength region of 1200-250 cm À1 .…”
Section: Magnesium Borate Mineralsmentioning
confidence: 99%
“…For the hydrated forms of magnesium borates, the stretching for polyanion of [B 6 O 7 (OH) 6 ] À2 and [B 3 O 3 (OH) 4 ] À2 is seen between 750 and 620 cm À1 . The "bending of B (3) -O" and "bending of B (4) -O" can be seen in the Raman shift wavelength ranges of 620-500 cm À1 and 500-250 cm À1 , respectively [6,7,9].…”
Section: Magnesium Borate Mineralsmentioning
confidence: 99%
“…Water is selected as the solution medium in liquid-state conditions; however, other types of fuels could also be used in metal borate preparation. The liquid-state synthesis procedure could also be entitled as hydrothermal, combustion, and co-precipitation methods [42][43][44]. The capping agent is usually added to the mixture of the dissolved sources.…”
Section: Synthesis Proceduresmentioning
confidence: 99%
“…The second step is called dehydroxilation which is removal hydroxyl groups on a compound as water molecules. Dehydration behaviors for different kinds of metal borates were studied in literature; and the thermal parameters were calculated [5,6].…”
Section: Introductionmentioning
confidence: 99%