Published at : 27 Dec 2017
Volume : IJtech
Vol 8, No 8 (2017)
DOI : https://doi.org/10.14716/ijtech.v8i8.738
Ahmad Fadli | Department of Chemical Engineering, Universitas Riau |
Amun Amri | Department of Chemical Engineering, Universitas Riau |
Esty Octiana Sari | Department of Chemical Engineering, Universitas Riau |
Iwantono | Department of Physics, Universitas Riau |
Arisman Adnan | Department of Mathematics, Universitas Riau |
Magnetite nanoparticles (Fe3O4) are a type of magnetic particle with huge potential for application as a drug carrier due to their excellent superparamagnetic, biocompatible, and easily modified surface properties. One characteristic of nanoparticles is that they can be controlled by studying the evolution of crystal growth. The purpose of this research is to study the evolution of magnetite-crystal growth and determine the crystal growth kinetics using the Ostwald ripening model. Magnetite nanoparticles were synthesized from FeCl3, citrate, urea, and polyethylene glycol using the hydrothermal method at 220oC for times ranging from 1–12 hours. The characterizations using X-ray diffraction (XRD) indicated that the magnetite began to form after 3 hours synthesis. The crystallinity and crystal size of the magnetite increased with the reaction time. The diameter size of the magnetite crystals was in the range of 10–29 nm. The characterizations using a transmission electron microscope (TEM) showed that magnetite nanoparticles had a relatively uniform size and were not agglomerated. The core-shell nanoparticles were obtained after 3 hours synthesis and had a diameter of 60 nm, whereas the irregular-shaped nanoparticles were obtained in 12 hours and had a diameter of 50 nm. The characterizations using a vibrating sample magnetometer (VSM) revealed that magnetite nanoparticles have superparamagnetic properties. The magnetization saturation (Ms) value was proportional to the degree of crystallinity. The magnetite-crystal growth data can be fitted to an Ostwald ripening model with the growth controlled by the dissolution of the surface reaction (n?4).
Crystal growth; Hydrothermal; Magnetite; Nanoparticles; Ostwald ripening
In conclusion, we have developed a facile, one-pot hydrothermal method for the synthesis of magnetite nanoparticles with a core-shell structure. The magnetite nanoparticles we obtained have monodispersity, no agglomeration, and a diameter of 50–60 nm. The magnetite nanoparticles also exhibited superparamagnetic properties, high saturation magnetization (65 emu/g), and were highly water soluble, which makes them an ideal candidate for drug delivery. The crystal growth kinetics study discovered a correlation among reaction time, crystal size, crystallinity, and magnetization saturation. A longer reaction time will increase the crystals’ sizes and crystallinity. In addition, the value of the saturation magnetization grew with increasing crystallinity. The magnetite-crystal growth data can be fitted to an Ostwald ripening model with the growth being controlled by the dissolution of the surface reaction (n?4), with a percentage error of 2.53%.
Financial support for this study was provided by the Ministry of Research, Technology and Higher Education of the Republic of Indonesia (Kemenristekdikti).
Arruebo, M., Pacheco, F.R., Ibarra, R.M., Santamaría, J., 2007. Magnetics Nanoparticles for Drug Delivery. Nanotoday, Volume 2(3), pp. 22–32
Bae, H.Y., Park, K., 2011. Targeted Drug Delivery to Tumors: Myths, Reality and Possibility. Journal of Control Release, Volume 153, pp. 198–205
Cao, X., Zhang, B., Zhao, F., Feng, L., 2012. Synthesis and Properties of MPEG-Coated Superparamagnetic Magnetite Nanoparticles. Journal of Nanomaterials, Volume 607296, pp. 1–6
Cheng, W., Tang, K., Qi, Y., Sheng, J., Liu, Z., 2010. One-step Synthesis of Superparamagnetic Monodisperse Porous Fe3O4 Hollow. Journal of Material Chemistry, Volume 2, pp. 1799–1805
Fitriana, N.K., Hafizah, E.A.M., Manaf, A., 2017. Synthesis and Magnetic Characterization of Mn-Ti Substituted Sr0.6Fe2-xMnx/2Tix/2O3 (x= 0.0-1.0) Nanoparticles by Combined Destruction Process. International Journal of Technology, Volume 8(4), pp. 644–650
Huang, F., Zhang, H., Banfield, F.J., 2003. Two-stage Crystal-growth Kinetics Observed during Hydhrothermal Coarsening of Nanocrystalline ZnS. Nano Letters, Volume 3, pp. 373–378
Hwang, N.M., Jung, S.J., Lee, K.D., 2012. Thermodynamics – Fundamentals and Its Application in Science: Chapter 14: Thermodynamics and Kinetics in the Synthesis of Monodisperse Nanoparticles, Korea, National Research Foundation of Korea (NRF)
International Union against Cancer (IUCC), 2009. 48th ICCA Congress & Exhibition Monday 9 November 2009, Available online at http://www.iccaworld.com/, Accessed on 5 April 2016
Khalil, M., Liu, N., Lee, L.R., 2017. Synthesis and Characterization of Hematite Nanoparticles using Ultrasonic Sonochemistry Method. International Journal of Technology, Volume 8(4), pp. 582–590
Luszczyk, K., Kaleta, J., Mech, R., 2014. Magnetic Core-shell Structures as Potential Carriers in Drug Delivery System. International Journal of Engineering Science, Volume 1, pp. 1–4
Marolt, M, 2014. Superparamagnetic Materials. In: Proceeding of Seminar Ib-4th Year (Old Program), University of Ljubljana Faculty of Mathematics and Physics 2014. Kranj, 23 April
Mohapatra, M., Anand, S., 2010. Synthesis and Applications of Nano-structured Iron Oxides/hydroxides – A Review. International Journal of Engineering, Science and Technology, Volume 2(8), pp. 127–146
Monshi, A., Foroughi, M.R, Monshi, M.R., 2012. Modified Scherrer Equation to Estimate More Accurately Nano-crystallite Size using XRD. Journal of Nano Science and Engineering, Volume 2, pp. 154–160
Qiao, R., Yang, C., Gao, M., 2009. Superparamagnetic Iron Oxide Nanoparticles: from Preparations to In Vivo MRI Applications. Journal of Material Chemistry, Volume 19, pp. 6274–6293
Thanh, N.T., K., Maclean, N., Mahiddine, S., 2014. Mechanisms of Nucleation and Growth of Nanoparticles in Solution. American Chemical Society: Chemical Reviews, Volume 114, pp. 7610?7630
Yu, M., Huang, S., Yu, K.J., Clyne, A.M., 2012. Dextran and Polymer Polyethylene Glycol (PEG) Coating Reduce Both 5 and 30 nm Iron Oxide Nanoparticle Cytotoxicity in 2D and 3D Cell Culture. International Journal of Molecular Science, Volume 13, pp. 5554–5570
Zhang, J., Hang, F., Lin, Z., 2010. Progress of Nanocrystalline Growth based on Oriented Attachment. The Royal Society of Chemistry: Nanoscale, Volume 2, pp. 18–34