TY - JOUR
T1 - Optimization of LaPO4 Synthesis and Characterization by Sol Gel Method
AU - Ulfindrayani, Ika F.
AU - Nurfia, Ina
AU - Murwani, Irmina K.
AU - Zulys, Agustino
AU - Kurniawan, Fredy
AU - Jovita, Stella
N1 - Publisher Copyright:
© 2024 American Institute of Physics Inc.. All rights reserved.
PY - 2024/6/7
Y1 - 2024/6/7
N2 - Lanthanum phosphate was successfully synthesized by sol-gel method at room temperature. The effect of pH, mole ratio of La:P, and aging time on Lanthanum phosphate formed were investigated. The optimization showed that Lanthanum phosphate is formed at pH 9, the mole ratio of La3+:PO43- is 1:1, and the aging time is 72 h. Then, the obtained powder was calcined at 550℃. The structure and chemical bond of the obtained powder were characterized using X-Ray Diffraction and Fourier Transform Infrared (FTIR) spectroscopy, respectively. The surface area was measured using N2 adsorption-desorption method. The morphology was analyzed using scanning electron microscopy (SEM). The XRD result showed that the obtained powder was Lanthanum phosphate which had a monoclinic structure. The FTIR spectra showed the presence of O-H functional at 3700-3450 cm-1 which was confirmed by the H-O-H bending vibration that appeared at 1650 cm-1. The peaks at 1040, 616, and 540 cm-1 indicated the presence of P-O stretching, O=P-O, and O-P-O bending. The N2 adsorption-desorption showed that Lanthanum phosphate formed was mesoporous materials with SBET of 93,28 m2/g. SEM images showed that agglomerated solids with irregular shapes were obtained from the synthesis.
AB - Lanthanum phosphate was successfully synthesized by sol-gel method at room temperature. The effect of pH, mole ratio of La:P, and aging time on Lanthanum phosphate formed were investigated. The optimization showed that Lanthanum phosphate is formed at pH 9, the mole ratio of La3+:PO43- is 1:1, and the aging time is 72 h. Then, the obtained powder was calcined at 550℃. The structure and chemical bond of the obtained powder were characterized using X-Ray Diffraction and Fourier Transform Infrared (FTIR) spectroscopy, respectively. The surface area was measured using N2 adsorption-desorption method. The morphology was analyzed using scanning electron microscopy (SEM). The XRD result showed that the obtained powder was Lanthanum phosphate which had a monoclinic structure. The FTIR spectra showed the presence of O-H functional at 3700-3450 cm-1 which was confirmed by the H-O-H bending vibration that appeared at 1650 cm-1. The peaks at 1040, 616, and 540 cm-1 indicated the presence of P-O stretching, O=P-O, and O-P-O bending. The N2 adsorption-desorption showed that Lanthanum phosphate formed was mesoporous materials with SBET of 93,28 m2/g. SEM images showed that agglomerated solids with irregular shapes were obtained from the synthesis.
UR - http://www.scopus.com/inward/record.url?scp=85196083452&partnerID=8YFLogxK
U2 - 10.1063/5.0214317
DO - 10.1063/5.0214317
M3 - Conference article
AN - SCOPUS:85196083452
SN - 0094-243X
VL - 3132
JO - AIP Conference Proceedings
JF - AIP Conference Proceedings
IS - 1
M1 - 050009
T2 - 3rd International Conference on Natural Sciences, Mathematics, Applications, Research, and Technology, ICON-SMART 2022
Y2 - 3 June 2022 through 4 June 2022
ER -