화학공학소재연구정보센터
Clean Technology, Vol.26, No.4, 251-256, December, 2020
Markable Green Synthesis of Gold Nanoparticles Used As Efficacious Catalyst for the Reduction of 4-Nitrophenol
E-mail:
The biocompatibility and plasmonic properties of Au nanoparticles make them useful for photothermal therapy, drug delivery, imaging, and many other fields. This study demonstrated a novel, facile, economic, and green synthetic method to produce gold nanoparticles. Gold nanoparticles (AuNPs) with spherical and triangular shapes were effectively synthesized using only Schisandra chenesis fruit extract as the capping and reducing agent. The shape of the AuNPs could be engineered simply by adjusting the molar concentration of HAuCl4 in the reaction mixture. The as-synthesized AuNPs were characterized using UV-VIS spectroscopy, transmission electron microscopy (TEM), X-ray diffraction (XRD), dynamic light scattering (DLS), and energy dispersive X-ray analysis (EDXA). This study revealed that by using the HAuCl4 concentration in the AuNP synthesis, the shape and size of the AuNPs could be controlled by the concentration of HAuCl4 and Schisandra chinensis fruit extract as a surfactant. The as-synthesized AuNPs samples had sufficient colloidal stability without noticeable aggregation and showed the predominant growth of the (111) plane of face-centered cubic gold during the crystal growth. The catalytic efficiency of the AuNPs synthesized using Schisandra chenesis fruit extract was examined by monitoring the catalytic reduction of 4-nitrophenol to 4-aminophenol using Ultraviolet-visible spectroscopy (UV-Vis spectroscopy). The synthesized AuNPs showed good catalytic activity to reduce 4-nitrophenol to 4-aminophenol, revealing their practical usefulness.
  1. Zhang QA, Li WY, Moran C, Zeng J, Chen JY, Wen LP, Xia YN, J. Am. Chem. Soc., 132(32), 11372 (2010)
  2. Pietrobon B, Kitaev V, Chem. Mater., 20, 5186 (2008)
  3. Zhang JA, Langille MR, Mirkin CA, J. Am. Chem. Soc., 132(35), 12502 (2010)
  4. Crespo-Biel O, Ravoo BJ, Huskens J, Reinhoudt DN, Dalton. Trans., 23, 2737 (2006)
  5. Gupta K, Jana PC, Meikap AK, Synth. Met., 160(13), 1566 (2010)
  6. Liz-Marzan LM, Langmuir, 22(1), 32 (2006)
  7. Manivasagan P, Bharathiraja S, Moorthy MS, Oh YO, Song K, Seo H, Oh J, ACS Appl. Interfaces, 9(17), 14633 (2017)
  8. Manivasagan P, Bharathiraja S, Bui NQ, Jang B, Oh YO, Lim IG, Oh J, Int. J. Biol. Macromol., 91, 578 (2016)
  9. Sun H, Yuan Q, Zhang B, Ai K, Zhang P, Lu L, Nanoscale, 3, 1990 (2011)
  10. Xia Y, Xiong Y, Lim B, Skrabalak SE, Angew. Chem.-Int. Edit., 48, 60 (2009)
  11. Varma RS, Current Opinion in Chem. Eng. 1(2), 123-128 (2012).
  12. Rokade AA, Kim JH, Lim SR, Yoo SI, Jin YE, Park SS, J. Clus. Sci., 28(4), 2017 (2017)
  13. Patil MP, Ngabire D, Thi HHP, Kim MD, Kim GD, J. Clus. Sci., 28(1), 119 (2017)
  14. Patil MP, Rokade AA, Ngabire D, Kim GD, J. Clus. Sci., 27(5), 1737 (2016)
  15. Sharma RK, Gulati S, Mehata S, J. Chem. Educ., 89, 1316 (2012)
  16. Shankar SS, Rai A, Ahmad A, Sastry M, Chem. Mater., 17(3), 566 (2005)
  17. Xie J, Lee JY, Wang DIC, J. Phys. Chem. C, 111, 10226 (2007)
  18. El-Seedi HR, El-Shabasy RM, Khalifa SAM, Saeed A, et al., RSC Adv., 9, 24539 (2019)
  19. Yong C, Jinbao T, Xiaoke W, Fengxiang S, Shujuan L, Inter. J. Biol. Macromol, 50(3), 844 (2012)
  20. Tafesh AM, Weiguny J, Chem. Rev., 96(6), 2035 (1996)
  21. Esumi K, Isono R, Yoshimura T, Langmuir, 20(1), 237 (2004)
  22. Pradhan N, Pal A, Pal T, Colloids Surf. A: Physicochem. Eng. Asp., 196(2), 247 (2002)
  23. Philip D, Spectroc. Acta Pt. A-Molec. Biomolec. Spectr., 77, 807 (2010)
  24. Liang M, Su R, Huang R, Qi W, Yu Y, Wang L, He Z, ACS Appl. Mater. Interfaces, 6(7), 4638 (2014)