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Preparation and Characterization of Zirconia Nanomaterial as a Molybdenum-99 Adsorbent

Atom Indonesia · Vol. 43 No. 1 (2017) · hlm. 1–6

DOI
10.17146/aij.2017.587
ISSN
2356-5322, 0126-1568
Terbit
2017-06-21
Penerbit
National Research and Innovation Agency
Bahasa
eng
Lisensi
creativecommons.org/licenses/by-nc-sa/4.0

Abstrak

The present study deals with the synthesis and characterization of ZrO2 nanomaterial which can be used as an adsorbent for Molybdenum-99 (99Mo). The adsorbent can potentially be utilized as the material for 99Mo/99mTc generator column. Using the sol-gel method, monoclinic nanocrystalline zirconia was synthesized from zirconium oxychloride in isopropyl alcohol reacted with ammonium hydroxide solution in isopropyl alcohol resulting in a white gel. The gel was subsequently refluxed for 12 hours at ~95°C and pH at ~4 and then dried at 100°C. The drying gel was then calcined at 600°C for two hours. Meanwhile the orthorhombic nanocrystalline zirconia was obtained by reacting zirconium oxychloride solution with 2.5 M ammonium hydroxide solution which resulted in a white gel. The gel was then refluxed for 24 hours at ~95°C and pH at ~11 and then dried at 100°C. The drying gel was then calcined at 600°C for two hours. These materials were characterized using FT-IR spectroscopy, X-ray diffraction (XRD), and Transmission Electron Microscope (TEM). The Scherrer method is used for determination of crystallite size. The FT-IR spectra for both materials show absorption peak at 450-500 cm-1 which are attributed to Zr-O bond. The XRD pattern of monoclinic nanocrystalline form shows crystalline peaks at 2θ regions of 28.37°, 31.65°, 34°, 36°, and 50.3° with average crystallite size of 2.68 nm. Meanwhile, the XRD pattern of orthorhombic nanocrystalline form shows crystalline peaks at 2θ regions of 30°, 35°, 50°, and 60° with average crystallite size of 0.98 nm. The TEM micrograph indicates that the zirconia nanomaterials prepared were quite uniform in size and shape.Received: 12 November 2015; Revised: 9 September 2016; Accepted: 20 September 2016

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  • National Nuclear Energy Agency of Indonesia
  • Dharmais Cancer Hospital
  • Pancasila University
  • Japan Atomic Energy Agency
  • University of Indonesia
  • Padjadjaran University
  • Chiyoda Technol Corporation (Japan)
  • Organisasi lain
  • Organisasi berbeda
  • Organisasi sama
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Tampilkan sebagai tabel
Rekan penulisOrganisasiArtikel bersama
A AbidinNational Nuclear Energy Agency of Indonesia15
Enny LestariNational Nuclear Energy Agency of Indonesia11
Abdul MutalibPadjadjaran University10
Hotman LubisNational Nuclear Energy Agency of Indonesia10
Sunarhadijoso SoenarjoNational Nuclear Energy Agency of Indonesia3
H HambaliNational Nuclear Energy Agency of Indonesia3
K. NishikataJapan Atomic Energy Agency3
Siska FebrianaNational Nuclear Energy Agency of Indonesia3
Rohadi AwaludinNational Nuclear Energy Agency of Indonesia3
M. TǎnaseChiyoda Technol Corporation (Japan)3
Kunihiko TsuchiyaJapan Atomic Energy Agency3
S.E. PermatasariUniversity of Indonesia2
Umi Nur SholikhahNational Nuclear Energy Agency of Indonesia2
Rezi Riadhi SyahdiUniversity of Indonesia2
Triani WidyaningrumNational Nuclear Energy Agency of Indonesia2
Hambali HambaliNational Nuclear Energy Agency of Indonesia2
Wira Y. RahmanNational Nuclear Energy Agency of Indonesia2
Triyanto TriyantoNational Nuclear Energy Agency of Indonesia2
Chandra WijayaPancasila University1
R ElzanPancasila University1
Fernanto RindiyantonoNational Nuclear Energy Agency of Indonesia1
Arni AriesNational Nuclear Energy Agency of Indonesia1
Yusuf Valentino KanetiNational Institute for Materials Science1
Muhammad IqbalBandung Institute of Technology1
Rajiman RajimanNational Nuclear Energy Agency of Indonesia1
Imam KambaliNational Nuclear Energy Agency of Indonesia1
Heranudin HeranudinNational Nuclear Energy Agency of Indonesia1
Parwanto ParwantoNational Nuclear Energy Agency of Indonesia1
Kardinah KardinahDharmais Cancer Hospital1
Nur HudaDharmais Cancer Hospital1
Ferdi Dwi ListiawadiDharmais Cancer Hospital1
Herta AstarinaDharmais Cancer Hospital1
Ratu Ralna IsmuhaDharmais Cancer Hospital1

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Sumber metadata: OAI-PMH (metadata jurnal) https://atomindonesia.brin.go.id/index.php/aij/oai, pertama di-harvest 8 Nov 2026, terakhir terlihat 8 Nov 2026.
Metadata asli (oai_dc)
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	<dc:title xml:lang="en-US">Preparation and Characterization of Zirconia Nanomaterial as a Molybdenum-99 Adsorbent</dc:title>
	<dc:creator>Marlina, M</dc:creator>
	<dc:creator>Sarmini, E.</dc:creator>
	<dc:creator>Herlina, H</dc:creator>
	<dc:creator>Sriyono, S</dc:creator>
	<dc:creator>Saptiama, I.</dc:creator>
	<dc:creator>Setiawan, H.</dc:creator>
	<dc:creator>Kadarisman, K</dc:creator>
	<dc:subject xml:lang="en-US">Nanozirconia; Sol-gel method; Adsorption capacity; Molybdenum-99</dc:subject>
	<dc:description xml:lang="en-US">The present study deals with the synthesis and characterization of ZrO2 nanomaterial which can be used as an adsorbent for Molybdenum-99 (99Mo). The adsorbent can potentially be utilized as the material for 99Mo/99mTc generator column. Using the sol-gel method, monoclinic nanocrystalline zirconia was synthesized from zirconium oxychloride in isopropyl alcohol reacted with ammonium hydroxide solution in isopropyl alcohol resulting in a white gel. The gel was subsequently refluxed for 12 hours at ~95°C and pH at ~4 and then dried at 100°C. The drying gel was then calcined at 600°C for two hours. Meanwhile the orthorhombic nanocrystalline zirconia was obtained by reacting zirconium oxychloride solution with 2.5 M ammonium hydroxide solution which resulted in a white gel. The gel was then refluxed for 24 hours at ~95°C and pH at ~11 and then dried at 100°C. The drying gel was then calcined at 600°C for two hours. These materials were characterized using FT-IR spectroscopy, X-ray diffraction (XRD), and Transmission Electron Microscope (TEM). The Scherrer method is used for determination of crystallite size. The FT-IR spectra for both materials show absorption peak at 450-500 cm-1 which are attributed to Zr-O bond. The XRD pattern of monoclinic nanocrystalline form shows crystalline peaks at 2θ regions of 28.37°, 31.65°, 34°, 36°, and 50.3° with average crystallite size of 2.68 nm. Meanwhile, the XRD pattern of orthorhombic nanocrystalline form shows crystalline peaks at 2θ regions of 30°, 35°, 50°, and 60° with average crystallite size of 0.98 nm. The TEM micrograph indicates that the zirconia nanomaterials prepared were quite uniform in size and shape.Received: 12 November 2015; Revised: 9 September 2016; Accepted: 20 September 2016</dc:description>
	<dc:publisher xml:lang="en-US">National Research and Innovation Agency</dc:publisher>
	<dc:contributor xml:lang="en-US">National Nuclear Energy Agency of Indonesia</dc:contributor>
	<dc:date>2017-06-21</dc:date>
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	<dc:source xml:lang="en-US">Atom Indonesia; Vol 43, No 1 (2017): April 2017; 1-6</dc:source>
	<dc:source>2356-5322</dc:source>
	<dc:source>0126-1568</dc:source>
	<dc:source>10.55981/aij.v43i1</dc:source>
	<dc:language>eng</dc:language>
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	<dc:rights xml:lang="en-US">Copyright (c) 2016 Atom Indonesia</dc:rights>
	<dc:rights xml:lang="en-US">http://creativecommons.org/licenses/by-nc-sa/4.0</dc:rights>
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