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Photonic crystals in biology

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Poster Session, Tuesday, June 15<br />

Theme A1 - B702<br />

Biological and Green Synthesis of Silver Nanoparticles<br />

Mehrdad Forough 1 and Khalil Farhadi 2 *<br />

1 Department of Chemistry, Faculty of Science, Payam-e-Noor University, Khoy, Iran<br />

2 Department of Chemistry, Faculty of Science, Urmia University, Urmia, Iran<br />

Abstract -The synthesis of stable silver nanoparticles by bio-reduction method , us<strong>in</strong>g aqueous extract of Manna of hedysarum plant<br />

as reduc<strong>in</strong>g agent of Ag + to Ag 0 , and Soap-root (Acanthe phyllum bracteatum) plant extract as a stabiliz<strong>in</strong>g agent has been<br />

<strong>in</strong>vestigated. Various spectroscopic methods such as X – ray diffraction Analysis (XRD) , energy – dispersive spectroscopy (EDX) ,scann<strong>in</strong>g<br />

electron microscopy (SEM) and UV-Vis spectroscopy were used to characterize the nanoparticles obta<strong>in</strong>ed. The energy dispersive<br />

spectroscopy (EDX) of the nanoparticles dispersion confirmed the presence of element silver signal no peaks of the impurity were<br />

detected. Comparison of experimental results showed that the diameter of prepared nanoparticles <strong>in</strong> solution is about 29-68 nm.<br />

In recent years noble metal nanoparticles have been the<br />

subject of focused researches due to their unique optical,<br />

electronic, mechanical, magnetic and chemical properties that<br />

are significantly different from those of bulk materials [1].<br />

These special and unique properties could be attributed to<br />

their small sizes and large surface area. Many techniques of<br />

synthesiz<strong>in</strong>g silver nanoparticles have been reported, such<br />

as chemical reduction of silver ions <strong>in</strong> aqueous solutions,<br />

with or without stabiliz<strong>in</strong>g[2], chemical and photo reduction<br />

<strong>in</strong> reverse micelles[3]. S<strong>in</strong>ce noble metal nanoparticles, are<br />

widely applied to human contact<strong>in</strong>g area[4] there is a grow<strong>in</strong>g<br />

need to develop environmentally friendly processes of<br />

nanoparticles synthesis that do not use toxic chemicals.<br />

Biological methods of nanoparticles synthesis us<strong>in</strong>g<br />

microorganism[5-6], have been suggested as possible ecofriendly<br />

alternatives to chemical and physical methods.<br />

Sometimes , the synthesis of nanoparticles us<strong>in</strong>g plants or<br />

parts of plants could prove advantageous over other biological<br />

processes by elim<strong>in</strong>at<strong>in</strong>g the elaborate processes of<br />

ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g the microbial cultures [7].<br />

In the present work, we <strong>in</strong>vestigate the synthesis of stable<br />

silver nanoparticles with bio-reduction method us<strong>in</strong>g two<br />

plants that, one of them acts as a reduc<strong>in</strong>g agent and the<br />

other acts as a stabiliz<strong>in</strong>g agent. Aqueous extract of Soaproot<br />

( Acanthe phylum bracteatum ) was employed as a<br />

stabilizer and aqueous extract of Manna of hedysarum was<br />

employed as a reductant. In this work we also compared<br />

the synthesis of silver nanoparticles by monitor<strong>in</strong>g the<br />

conversion us<strong>in</strong>g UV – Vis spectroscopy.<br />

First, the aqueous extracts of plants were prepared by simple<br />

physicochemical methods, purified and then filtered. For<br />

preparation of silver nanoparticles, 10 ml of prepared<br />

extract of Soap-root ( Acanthe phylum bracteatum) plant as<br />

a stabiliz<strong>in</strong>g agent was added to 100 ml of 0.003 M<br />

aqueous AgNO 3 solution and after 5 m<strong>in</strong>, 15 ml of<br />

aqueous extract of manna of Hedysarum was added to<br />

mixture for reduction of Ag + ions. The silver nanoparticles<br />

solution thus obta<strong>in</strong>ed was purified by several centrifugation.<br />

After freeze dry<strong>in</strong>g of the purified silver nanoparticles ,the<br />

structure, composition and average size of the synthesized<br />

silver nanoparticles were analyzed by scann<strong>in</strong>g electron<br />

microscopy (SEM), X-ray diffraction spectroscopy (XRD) and<br />

energy dispersive X-ray microanalysis spectroscopy (EDX).<br />

Also the purified powders of silver nanoparticles were<br />

subjected to FT-IR spectroscopy measurement. It is well<br />

known that silver nanoparticles exhibit yellowish – brown<br />

color <strong>in</strong> aqueous solution due to excitation of surface<br />

plasmon vibrations <strong>in</strong> silver nanoparticles. Figure (a ) shows<br />

the photographs of samples .The silver conta<strong>in</strong><strong>in</strong>g solution<br />

(left flask) is colorless but changes to brownish color on<br />

completion of the reaction with manna of hedysarum<br />

extract (right flask).<br />

(a)<br />

Figure 1. ( a). Solution of silver nitrate (3 mM) before (left) and<br />

after (right) addition plant extract.(b) Scann<strong>in</strong>g electron<br />

micrograph of the silver nanoparticles obta<strong>in</strong>ed.<br />

The energy dispersive spectroscopy (EDX)of the<br />

nanoparticles dispersion confirmed the presence of element<br />

silver signal and no peaks of the impurity were detected.<br />

Scann<strong>in</strong>g electron microscopy has provided further <strong>in</strong>sight<br />

<strong>in</strong>to the morphology and size details of the silver<br />

nanoparticles. Comparison of experimental results, showed<br />

that the diameter of prepared nanoparticles <strong>in</strong> solution is<br />

about 29-68 nm.Figure (b) shows the scann<strong>in</strong>g electron<br />

micrograph of the of silver nanoparticles that obta<strong>in</strong>ed with<br />

treated 3.0 mM silver nitrate solution with plant extract <strong>in</strong><br />

86 °C for 13 m<strong>in</strong>.<br />

*Correspond<strong>in</strong>g author: 1Tkhalil.farhadi@yahoo.com1T<br />

[1] Mazur M. Electrochemistry Communications 6, 400 (2004).<br />

[2] Liz-Marzan LM, Lado-Tour<strong>in</strong>o . Langmuir 12, 3585 (1996).<br />

[3] Pileni MP, Pure Appl Chem 72, 53 (2000).<br />

[4] Jae YS, BEAM SK, Bioprocess Biosyst Eng 32, 79 (2009).<br />

[5] Klaus T ,Joerger R, Olsson E, Granqvist C-G, Proc Nalt Acad Sci<br />

crystall<strong>in</strong>e USA 96, 13611(1999).<br />

[6] Konishi Y , Uruga T,J Biotechnol 128, :648 (2007).<br />

[7] Shankar SS, Rai A, Ahmad A, Sastry M, J Colloid Interface Sci<br />

275, 496 (2004).<br />

(b)<br />

6th Nanoscience and Nanotechnology Conference, zmir, 2010 286

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