2012
DOI: 10.1016/j.jssc.2012.07.019
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From dihydrated iron(III) phosphate to monohydrated ammonium–iron(II) phosphate: Solvothermal reaction mediated by acetone–urea mixtures

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Cited by 8 publications
(3 citation statements)
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“…Throughout the literature researches, the advantages of using urea as an additive are as follows: (i) The two ‐NH 2 groups in urea are alkaline. The alkaline groups can improve the pH value of the reaction and be used for the complexation of the metal ions in the solution, which makes it easier to reach the growth interface, thus increasing the growth rate of crystal ,. (ii) The N atom in urea can coordinate with the Fe atom in lithium iron phosphate, which affects the crystal growth to control the material morphology.…”
Section: Introductionmentioning
confidence: 99%
“…Throughout the literature researches, the advantages of using urea as an additive are as follows: (i) The two ‐NH 2 groups in urea are alkaline. The alkaline groups can improve the pH value of the reaction and be used for the complexation of the metal ions in the solution, which makes it easier to reach the growth interface, thus increasing the growth rate of crystal ,. (ii) The N atom in urea can coordinate with the Fe atom in lithium iron phosphate, which affects the crystal growth to control the material morphology.…”
Section: Introductionmentioning
confidence: 99%
“…Among them, the band at 1738 cm −1 (attributed to the acetyl and uronic ester groups or the ester linkage of the carboxylic group of ferulic and p‐coumaricacid of hemicellulose), 1600 cm −1 and 1510 cm −1 (arising from the aromatic skeletal vibration), 1460 cm −1 (assigned to C−H deformation combined with aromatic ring vibration), and 1250 cm −1 (corresponding to methoxyl groups of lignin) . The bands (Figure , d) between 1150 and 920 cm −1 are due to the P−O stretching vibrations, while the two bands at around 625 and 550 cm −1 are related to the O−P‐O bending vibrations ,,…”
Section: Resultsmentioning
confidence: 99%
“…This synthesis, carried out at 180 °C, has successfully afforded the target compound as hierarchical microspheres. Further, regarding iron phosphates, Alfonso et al 539 used hydrothermal synthesis involving FeCl 2 and urea at 180 °C to prepare the phosphate and further subjected the compound to solvothermal treatment at 180 °C in acetone, yielding the transformation of FePO 4 to (NH 4 )FePO 4 •H 2 O.…”
Section: Also Provide Several Further Examplesmentioning
confidence: 99%