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Physical properties and antioxidant activity of ZnO nanoparticles synthesized by Moringa oleifera leaf extract at different pH values

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초록

We have demonstrated green synthesis of ZnO nanoparticles using Moringa oleifera leaves (Mor-ZnO NPs) extractby co-precipitation method under 450oC for 2 hours with different pH-5, pH-7, and pH-8. The physical properties (i.e. structural, morphology, and absorbance) have been analyzed using X-ray diffraction (XRD) measurement, scanning electronmicroscopy (SEM), and ultraviolet-visible (UV-Vis) spectrophotometer. Furthermore, to investigate the functional group andantioxidant activity we performed Fourier transform infra-red (FTIR) analysis and 2,2-diphenyl-1-picrylhydrazyl (DPPH)assay. Structurally, all samples possess polycrystalline hexagonal wurtzite structure. Morphologically, the pH values affectthe morphology of Mor-ZnO NPs. Optically, the Mor-ZnO NPs with pH-8 have strong absorption in the range of shortultraviolet (200-280 nm). We predict that the basic pH value on green synthesize of Mor-ZnO NPs tune the near band edgeabsorption (NBA), which relates to the recombination of the free excitons. Whereas, based on the FTIR spectra analysis, theZn-O stretching can be identified at 442.67 cm-1, 458.67 cm-1, and 442.67 cm-1 for Mor-ZnO NPs with the pH-5, pH-7, andpH-8, respectively. According to DPPH assay, the Mor-ZnO NPs with pH-8 at 200 mg/ml has higher inhibition rate (67.7%). Hence, we believed that the Mor-ZnO NPs are potential antioxidants.

Abstract

We have demonstrated green synthesis of ZnO nanoparticles using Moringa oleifera leaves (Mor-ZnO NPs) extractby co-precipitation method under 450oC for 2 hours with different pH-5, pH-7, and pH-8. The physical properties (i.e. structural, morphology, and absorbance) have been analyzed using X-ray diffraction (XRD) measurement, scanning electronmicroscopy (SEM), and ultraviolet-visible (UV-Vis) spectrophotometer. Furthermore, to investigate the functional group andantioxidant activity we performed Fourier transform infra-red (FTIR) analysis and 2,2-diphenyl-1-picrylhydrazyl (DPPH)assay. Structurally, all samples possess polycrystalline hexagonal wurtzite structure. Morphologically, the pH values affectthe morphology of Mor-ZnO NPs. Optically, the Mor-ZnO NPs with pH-8 have strong absorption in the range of shortultraviolet (200-280 nm). We predict that the basic pH value on green synthesize of Mor-ZnO NPs tune the near band edgeabsorption (NBA), which relates to the recombination of the free excitons. Whereas, based on the FTIR spectra analysis, theZn-O stretching can be identified at 442.67 cm-1, 458.67 cm-1, and 442.67 cm-1 for Mor-ZnO NPs with the pH-5, pH-7, andpH-8, respectively. According to DPPH assay, the Mor-ZnO NPs with pH-8 at 200 mg/ml has higher inhibition rate (67.7%). Hence, we believed that the Mor-ZnO NPs are potential antioxidants.

참고문헌 (23)

  1. S. Iwan, , AIP Conf. Proc, 1729, pp.020031~ (2016)
  2. S. T. Tan, , Appl. Phys. Lett, 93, pp.013506~ (2008)
  3. S. Raha, , Nanoscale Adv, 4, pp.1868~1925 (2022)
  4. D. Sogets, , ACS Nano, 3(7), pp.1703~1710 (2009)
  5. Z. L. Wang, , ACS Nano, 2(10), pp.1987~1992 (2008)
  6. S. Mirza, , Inorg. Chem. Commun, 155, pp.111124~ (2023)
  7. H. A. Jabri, , Life, 12(4), pp.594~ (2022)
  8. F. K. Konan, , J. Ceram. Process. Res, 20(4), pp.372~378 (2019)
  9. J. Moghaddam, , J. Ceram. Process. Res, 14(4), pp.459~462 (2013)
  10. S. S. Salem, , Biol. Trace Elem. Res, 199, pp.344~370 (2021)
  11. I. Ngom, , Mater. Today : Proc, 36(2), pp.526~533 (2021)
  12. H. R. Vasanthi, , Curr. Med. Chem, 19(14), pp.2242~2251 (2012)
  13. M. Sondergaard, , Cryst. Growth Des, 11(9), pp.4027~4033 (2011)
  14. V. Vinotha, , J. Photochem. and Photobiol. B, 197, pp.111541~ (2019)
  15. N. Matinise, , Appl. Surf. Sci, 406, pp.339~347 (2017)
  16. K. Velsankar, , J. Mol. Struct, 1255, pp.132420~ (2022)
  17. B. Gherbi, , Sustainabillity, 14(18), pp.11300~ (2022)
  18. S. S. Alias, , J. Alloys. Compd, 499(2), pp.231~237 (2010)
  19. S. Iwan, , J. Ceram. Process. Res, 20(5), pp.518~521 (2019)
  20. A. K. Zak, , Ceram. Int, 37(1), pp.393~398 (2011)
  21. J. H. Koo, , J. Ceram. Process. Res, 18(2), pp.156~160 (2017)
  22. I. Sugihartono, , Mat. Res, 26, pp.0499~ (2023)
  23. D. Rehana, , Bioprocess Biosyst. Eng, 40, pp.943~957 (2017)

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