Green synthesis of silver nanoparticles from aqueous Aegle marmelos leaf extract
Source abstract
Abstract
Abstract Synthesis of nanoparticles by green route is an emerging technique drawing more attention recently because of several advantages over the convention chemical routes. The present study reports one-pot synthesis and in situ stabilization of silver nanoparticles using Aegle marmelos leaf extract. Nanoparticles of almost uniform spherical size (∼60 nm) were synthesized within ∼25 min reaction time at room temperature. The size of particles depends on the ratio of AgNO 3 and leaf extract. The crystallinity, size, and shape of the nanoparticles were characterized by X-ray diffraction, dynamic light scattering, and scanning electron microscopy respectively. The size stability was attained by the capping effect of polyphenolic tannin compound, procatacheuate in the extract. The capped polyphenols can be removed from the particle surface by simple NaOH/methanol wash. The involvement of phenolic compounds in metal ion reduction and capping were supported by UV–visible spectroscopy, infrared spectroscopy, high performance liquid chromatography, and zeta potential measurements.
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Research context
OpenAlex topics: Nanoparticles: synthesis and applications · Laser-Ablation Synthesis of Nanoparticles · Nanotechnology research and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (45)
Show source-provided references
1. Magdassi · Chem. Mater. · 2003 · 15 · 220810.1021/cm021804b ↗
2. Jain · Biotechnol. Bioeng. · 2005 · 90 · 5910.1002/bit.20368 ↗
3. Prasad · Curr. Nanosci. · 2011 · 7 · 53110.2174/157341311796196736 ↗
4. Sintubin · Appl. Microbiol. Biotechnol. · 2009 · 84 · 74110.1007/s00253-009-2032-6 ↗
5. Zaki · Mater. Res. Bull. · 2011 · 46 · 157110.1016/j.materresbull.2011.06.025 ↗
6. Gajbhiye · Nanomedicine: NBM · 2009 · 5 · 38210.1016/j.nano.2009.06.005 ↗
7. Jha · Colloids Surf. B · 2009 · 71 · 22610.1016/j.colsurfb.2009.02.007 ↗
8. Jebali · J. Clust. Sci. · 2011 · 22 · 22510.1007/s10876-011-0375-5 ↗
9. Ingle · J. Nanoparticle Res. · 2008 · 11 · 207910.1007/s11051-008-9573-y ↗
10. Dahl · Chem. Rev. · 2007 · 107 · 222810.1021/cr050943k ↗
11. Mohammed Fayaz · Process Biochem. · 2011 · 46 · 195810.1016/j.procbio.2011.07.003 ↗
12. Shankar · J. Colloid Interface Sci. · 2004 · 275 · 49610.1016/j.jcis.2004.03.003 ↗
13. Krishnaraj · Colloids Surf. B · 2010 · 76 · 5010.1016/j.colsurfb.2009.10.008 ↗
14. Begum · Colloids Surf. B · 2009 · 71 · 11310.1016/j.colsurfb.2009.01.012 ↗
15. Song · Bioprocess Biosyst. Eng. · 2009 · 32 · 7910.1007/s00449-008-0224-6 ↗
16. Huang · Nanotechnology · 2007 · 18 · 10510410.1088/0957-4484/18/10/105104 ↗
17. Raut · Nano-Micro Lett. · 2010 · 2 · 10610.5101/nml.v2i2.p106-113 ↗
18. Sathishkumar · Bioresour. Technol. · 2010 · 101 · 795810.1016/j.biortech.2010.05.051 ↗
19. Sathishkumar · Colloids Surf. B · 2009 · 73 · 33210.1016/j.colsurfb.2009.06.005 ↗
20. Raghunandan · Colloids Surf. B · 2010 · 79 · 23510.1016/j.colsurfb.2010.04.003 ↗
21. Bali · 2006 · 224
22. Satyavani · J. Nanosci. Nanotechnol. · 2011 · 1 · 9510.3923/rjnn.2011.95.101 ↗
23. Jha · Colloids Surf. B · 2009 · 73 · 21910.1016/j.colsurfb.2009.05.018 ↗
24. Kumar · J. Chem. Technol. Biotechnol. · 2010 · 85 · 130110.1002/jctb.2427 ↗
25. Thakkar · Nanomedicine: NBM · 2010 · 6 · 25710.1016/j.nano.2009.07.002 ↗
26. Jacob · Colloids Surf. B · 2011 · 87 · 4910.1016/j.colsurfb.2011.04.036 ↗
27. Durán · Appl. Microbiol. Biotechnol. · 2011 · 90 · 160910.1007/s00253-011-3249-8 ↗
28. Clark · Green Chem. · 1999 · 1 · 110.1039/a807961g ↗
29. Sharma · Nat. Prod. Radiance · 2007 · 6 · 171
30. Maity · Ind. J. Exp. Biol. · 2009 · 47 · 849
31. Yadav · Nutraceut. Pharm. Rev. · 2009 · 144
32. Gokhale · 2008
33. Thimmaiah · 2003
34. Basova · J. Anal. Chem. · 2002 · 57 · 43410.1023/A:1015465710024 ↗
35. Chen · Chin. J. Polym. Sci. · 2002 · 20 · 309
36. Bulut · Ind. Eng. Chem. Res. · 2009 · 48 · 568610.1021/ie801779f ↗
37. Interpretation of infrared spectra, a practical approach
38. Zhao · Physica E · 2004 · 23 · 9210.1016/j.physe.2004.01.008 ↗
39. Theerasin · Asian J. Food Agro. Ind. · 2009 · 2 · 547
40. U. Huber, Analysis of Protocatechuic Acid, Protocatechuic Aldehyde and Tanshinones in Dan Shen Pills by HPLC, A Report by Agilent Technologies (www.chem.agilent.com/Library/applications/59682882.pdf), 1998.
41. Bartnik · J. Planar Chromatogr. – Mod. TLC · 2003 · 16 · 20610.1556/JPC.16.2003.3.7 ↗
42. Kumar · J. Sep. Sci. · 2008 · 31 · 26210.1002/jssc.200700372 ↗
43. Rangkadilok · J. Agric. Food Chem. · 2005 · 53 · 138710.1021/jf0403484 ↗
44. Yadav · J. Pharm. Res. · 2011 · 4 · 717
45. Sadowski · Mater. Sci. Poland · 2008 · 26 · 419