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Open Access

Peer-reviewed

Research Article

Using Hydrophilic Ionic Liquid, [bmim]BF4 – Ethylene Glycol System as a Novel Media for the Rapid Synthesis of Copper Nanoparticles

Abstract

In this work, we present a novel method for the synthesis of copper nanoparticles. We utilize the charge compensatory effect of ionic liquid [bmim]BF4 in conjunction with ethylene glycol for providing electro-steric stabilization to copper nanoparticles prepared from copper sulphate using hydrazine hydrate as a reducing agent. The formed copper nanoparticles showed extended stability over a period of one year. Copper nanoparticles thus prepared were characterized by powder X-ray diffraction measurements (pXRD), transmission electron microscopy (TEM) and quasi elastic light scattering (QELS) techniques. Powder X-ray diffraction (pXRD) analysis revealed relevant Bragg's reflection for crystal structure of copper. Powder X-ray diffraction plots also revealed no oxidized material of copper nanoparticles. TEM showed nearly uniform distribution of the particles in methanol and confirmed by QELS. Typical applications of copper nanoparticles include uses in conductive films, lubrication and nanofluids. Currently efforts are under way in our laboratory for using these nanoparticles as catalysts for a variety of organic reactions.

Citation: Dewan M, Kumar A, Saxena A, De A, Mozumdar S (2012) Using Hydrophilic Ionic Liquid, [bmim]BF4 – Ethylene Glycol System as a Novel Media for the Rapid Synthesis of Copper Nanoparticles. PLoS ONE 7(1): e29131. https://doi.org/10.1371/journal.pone.0029131

Editor: Vipul Bansal, RMIT University, Australia

Received: August 5, 2011; Accepted: November 21, 2011; Published: January 6, 2012

Copyright: © 2012 Dewan et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Funding: There are no current external funding sources for this study.

Competing interests: The authors have declared that no competing interests exist.

Introduction

Metal nanoparticles play a significant role in diverse fields such as optical, electronic, catalysis, medical, magnetic, information storage and surface enhanced raman scattering (SERS) [1]. Copper is one of the classic metal nanoparticle systems that has gained considerable attention in the past two decades due to its unusual properties, leading to potential applications in many fields. Non-agglomerated, spherical, uniform copper nanoparticles have been employed extensively for conductive films, lubrication, nanofluids, catalysis, etc. A number of methods such as microemulsion, reverse micelles, reduction of aqueous copper salts, gamma irradiation, UV light irradiation, protecting shells by Pileni et al, electrolytic techniques by controlling electrode potential and the polyol process have been developed for the preparation of copper metal nanoparticles [2]. Chen and Sommers have described a one phase system for the synthesis of copper nanoparticles with an alkanethiolate as a protecting monolayer [3]. Sonochemical method and thermal decomposition method have also been reported [4], [5]. However, the copper nanoparticles resulting from these methods had shortcomings, like limited size, monodispersity and are susceptible to oxidation. So there is a crucial need to develop a method to synthesize copper nanoparticles with prolonged stability and in this respect ionic liquids have developed as a source of potential rescue.

The use of Ionic Liquids (ILs) in science and its technological applications is not new as they have already emerged as a green alternative to the conventional and environmentally detrimental volatile solvents. They have attracted a great deal of attention due to their high thermal stability, good conductivity, non volatility, non flammability, suitable polarity, wide electrochemical window and recyclability [6]. Most importantly physical and chemical properties of ILs can be exploited by altering their cation, anion and attached substituents [7], [8]. Hence ILs have been used extensively and have great potentiality in the upcoming applications in sensors [9], material synthesis [10]–[12], separation and extraction [13], asymmetric synthesis [14], nuclear fuel cycle processing [15], liquid thermal storage media and heat transfer fluids [16], lubricants [17], etc.

Our study is focused towards the ionic liquids based on imidazolium cations as they are especially favorable for green industrial applications [18]. Their most important property being, although they are liquid at room temperature they are considered safer and more environmentally benign as unlike organic solvents they do not evaporate [19]. Imidazolium ILs provide an excellent medium for the formation and stabilization of transition metal nanoparticles. It is bcause of the negligible vapor pressure, the size and shape of metal nanoparticles can be investigated in situ by TEM [20], [21]. Moreover particles synthesized in organic solvents are usually immiscible in water and this also limits their applicability. Many applications require for nanoparticles to be dispersed and stable in water. However, water based synthesis of nanoparticles is fraught with many problems such as ionic interactions, low reactant concentration, and difficulty in removing the stabilizers [22]. Ionic liquids present an encompassing solution as both the cation and anion of an ionic liquid can potentially serve as charge compensating groups in the synthesis procedure. When an ionic liquid is used as a reaction media the solute is solvated by ions only. Thus, the reaction can proceed in an environment totally different from that when water or ordinary organic solvents are used. As a result, high selectivity is possible [23], [24]. This study provides an alternative to synthesizing nanomaterial with minimal energy consumption and high yield. Such metal nanoparticles has been previously demonstrated to efficiently catalyze a variety of organic reactions [25]–[29]. We report herein, well dispersed, size controlled synthesis of copper nanoparticles in ionic liquid - ethylene glycol system with hydrazine hydrate as reducing agent without the aid of any heating or microwave irradiation (Supporting Information S1).

Materials and Methods

1. Materials

Copper sulphate pentahydrate (CuSO4.5H2O), ethylene glycol, hydrazine hydrate (NH2NH2.2H2O), sodium tetrafluoroborate and 1-butyl-3-methylimidazoliumbromide were all of analytical grade and used as such. All the aldehydes and solvents were purchased from spectrochem Pvt. Ltd. Mumbai (India) and were used without any additional purification. All reactions were monitored by thin layer chromatography (TLC) on gel F254 plates. 1H-NMR and 13 C-NMR spectra were recorded in CDCl3 and DMSO-d6 on a Jeol JNN ECX- 400P spectrometer; Melting points were recorded on SECOR Laboratories instruments melting point instruments. The infrared spectra were recorded using a model Perkin Elmer spectrum BX2 FT-IR system. Spectra were recorded with Spectrum V 5.3.1 software in the range 4000–400 cm−1. The KBr pellet technique was adopted for recording the spectra.

2. Synthesis of ionic liquid [bmim]BF4

Sodium tetrafluoroborate and 1-butyl-3-methylimidazoliumbromide in equimolar quantities were stirred in dry acetone under anhydrous conditions for 48–72 h. The mixture was filtered off to remove unreacted sodium tetrafluoroborate and the filtrate was further treated with dichloromethane to remove sodium bromide and again the filtrate obtained was again treated with dichloromethane to check for any further precipitation. The solvents were removed under reduced pressure and the resulting colorless ionic liquid was dried in rotavapor at 70°C for 2 h to remove water. The product 1-butyl-3-methylimidazoliumtetrafuoroborate was characterized by 1H NMR studies. (Figure 1)

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Figure 1. Synthesis of ionic liquid [bmim]BF4 and preparation of copper nanoparticles.

https://doi.org/10.1371/journal.pone.0029131.g001

3. Preparation of copper nanoparticles in IL-Ethylene glycol media using hydrazine hydrate as reducing agent

In a typical experiment 5 ml ethylene glycol was used as the solvent and 100 µl of ionic liquid was added to it to give a final concentration of 1 M. This was followed by addition of 0.1 M CuSO4.5H2O (100 µl) and the reaction was allowed to stir on a magnetic stirrer under nitrogen atmosphere. After five minutes 3.0 M hydrazine hydrate (100 µl) was added as the reducing agent drop wise continued over a period of ten minutes and the system was stirred for another 30 minutes. (Figure 1). The mixture attained a uniform brown color without any aggregation. An aliquot amount of ‘ionic liquid-ethylene glycol’ protected copper nanoparticles were taken out and particle size distribution measurements were done using particle size analyzer (QELS, Photocor-FC, model-1135 P).

The particle synthesis procedure was repeated for a bulk set of 100 ml. Particles from the reaction mixture were centrifuged and washed with ethanol. The process of centrifuge and washing the particle was repeated thrice to afford powdered copper nanoparticles. Transmission electron microscope (TEM, FEI Technai 300 kV fitted with EDAX) was used to image size and morphology of the powder. X-ray diffraction patterns of the powders were recorded using diffractometer (Philips Analytica PW 1830 X-ray equipped with a 2θ compensting slits).

Results and Discussion

We report herein a method to synthesize stabilized copper nanoparticles using hydrazine hydrate as a reducing agent in the presence of ethylene glycol and [bmim]BF4. We discover that ionic liquid in conjunction with ethylene glycol play a vital role in the stabilization of copper nanoparticles.

Ionic liquid [bmim]BF4, serves as an excellent media for dispersing copper nanoparticles, controlling their size and preventing their aerial oxidation; however agglomeration could not be avoided in the absence of ethylene glycol. Nanoparticles could also be synthesized in ethylene glycol alone. But the synthesized nanoparticles are not stable for extended periods of time. The probable reason is that the synthesized nanoparticles are oxidized. We intend to use the synthesized nanoparticles for catalysts over multiple cycles and store them. Thus our aim is to make nanoparticles that are stable for extended periods of time. Thus, we find that both ethylene glycol and ionic liquid [bmim]BF4 is required for synthesizing stable, monodispersed nanoparticles. Using ethylene glycol alone in the absence of [bmim]BF4 gives unstable nanoparticles; whereas using [bmim]BF4 alone in the absence of ethylene glycol leads to agglomeration of nanoparticles. Furthermore, we determine that using hydrazine hydrate as a reducing agent in the presence of ethylene glycol and hydrophilic ionic liquid [bmim]BF4 could serve effectively to increase the reaction and nucleation rates without employing any source of heating or microwave irradiation.

Since the ionic liquid [bmim]BF4 is hydrophilic, there was the possibility of it absorbing moisture thereby rendering the nanoparticles unusable over long periods of time. Our experiments showed that the nanoparticles were stabilised for at least one year. Ionic liquid [bmim][BF4] has been demonstrated previously to be a moisture and thermally stable compound [30]. and has been used it in the solvothermal synthesis of the coordination polymer [Cu(I)(bpp)]BF4. Our results are in agreement with the previous work; the added stability could also be attributed to the use of an organic solvent like ethylene glycol.

Color changes during course of reduction indicate complex formation between copper sulphate and hydrazine hydrate. As the hydrazine hydrate solution is introduced drop wise, the blue color of copper sulphate solution turns darker and gradually turns intense yellow and eventually brown during the course of the reaction, indicating formation of highly dispersed metallic copper. UV-Vis spectra as shown in Fig. 2. It indicates formation of protected nanoparticles with λmax near 580 nm.

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Figure 2. UV-Visible spectra of Copper nanoparticles.

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Copper nanoparticles separated from the suspension were analyzed for their size distribution and shape by DLS and TEM. Alongside average sizes were calculated from XRD peak data. TEM images in Fig. 3 illustrates the formation of spherical, ‘ionic liquid-ethylene glycol’ protected copper nanoparticles with little agglomeration. Fig. 4 shows size distribution from the DLS data, revealing mean size of 40±3 nm in diameter with polydispersity index of 0.203. XRD patterns of the copper nanoparticles prepared from this procedure as plotted in Fig. 4, displays 2θ values from 20° to 90°. XRD pattern reflections correspond to that of pure copper (Fig. 5), shows three characteristic peaks at respectively corresponding to indices; (111), (200) and (220). These peaks accurately resemble impurity less and oxide less FCC copper phase.

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Figure 3. TEM images of Copper nanoparticles.

https://doi.org/10.1371/journal.pone.0029131.g003

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Figure 4. Dynamic Light Scattering data of copper nanoparticles.

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Figure 5. XRD plot of Copper nanoparticles.

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Discussion

Use of ionic liquid-ethylene glycol media for the synthesis of copper nanoparticles stabilised over a period of more than one year has been demonstrated. In the first step, there is an ion-exchange reaction where [bmim][Br] reacts with NaBF4 to give ionic liquid [bmim][BF4] and NaBr. The subsequent synthesis of Cu nanoparticles involves reduction of CuSO4.5H2O by hydrazine in the presence of the ionic liquid (Scheme 1). A simple, convenient and significant method for the reductive synthesis of copper nanoparticles in ionic liquid has thus been uncovered here.

Author Contributions

Conceived and designed the experiments: AK SM. Performed the experiments: MD AK AS. Analyzed the data: AD. Contributed reagents/materials/analysis tools: AK. Wrote the paper: MD AD.

References

  1. 1. Zhu J, Shen Y, Xie A, Qiu L, Zhang Q, et al. (2007) Photoinduced Synthesis of Anisotropic Gold Nanoparticles in Room-Temperature Ionic Liquid. J Phys Chem C 111: 7629–7633.
  2. 2. Zhu H, Zhang C, Yin Y (2005) Novel Synthesis of Copper Nanoparticles: Influence of the Synthesis Conditions on the Particle Size. Nanotechnology 16: 3079–3083.
  3. 3. Khanna PK, Gaikwad S, Adhyapak PV, Singh N, Marimuthu R (2007) Synthesis and characterization of copper nanoparticles. Materials Letters 61: 4711–4714.
  4. 4. Niasari MS, Davar F (2009) Synthesis of copper and copper(I) oxide nanoparticles by thermal decomposition of a new precursor. Materials Letters 63: 441–443.
  5. 5. Dhas NA, Raj CP, Gedanken A (1998) Synthesis, characterization and properties of metallic copper nanoparticles. Chem. Mater 10: 1446–1452.
  6. 6. He Y, Shen X (2008) Interaction between β-cyclodextrin and ionic liquids in aqueous solutions investigated by a competitive method using a substituted 3H-indole probe. Journal of Photochemistry and Photobiology A: Chemistry 197: 253–259.
  7. 7. Holomb R, Martinelli A, Albinsson I, Lassègues JC, Johansson P, et al. (2008) Ionic liquid structure: the conformational isomerism in 1-butyl-3-methyl-imidazolium tetrafluoroborate ([bmim][BF4]. J Raman Spectrosc 39: 793–805.
  8. 8. Trohalaki S, Pachter R (2005) Prediction of Melting Points for Ionic. Liquids QSAR Comb Sci 24: 485–490.
  9. 9. Kachoosangi RT, Musameh MM, Abu-Yousef I, Yousef JM, Kanan SM, et al. (2009) Carbon Nanotube−Ionic Liquid Composite Sensors and Biosensors. Anal Chem 81: 435–442.
  10. 10. Zhang J, Wang J, Zhou S, Duan K, Feng B, et al. (2010) Ionic liquid-controlled synthesis of ZnO microspheres. J Mater Chem 20: 9798–9804.
  11. 11. Redel E, Thomannb R, Janiak C (2008) Use of ionic liquids (ILs) for the IL-anion size-dependent formation of Cr, Mo and Wnanoparticles from metal carbonyl M(CO)6 precursors. Chem Commun 15: 1789–1791.
  12. 12. Zhang M, Xu X, Zhang M (2008) Microwave-Assisted Synthesis and Characterization of CuO · Nanocrystals Volume. Journal of Dispersion Science and Technology 29: 508–513.
  13. 13. Germani R, Mancini MV, Savelli G, Spreti N (2007) Mercury extraction by ionic liquids: temperature and alkyl chain length effect. Tetrahedron Letters 48: 1767–1769.
  14. 14. Paczal A, Kotschy A (2007) Asymmetric synthesis in Ionic Liquids. Monatshefte fur Chemie 138: 1115–1123.
  15. 15. Ha SH, Menchavez RN, Koo YM (2010) Reprocessing of spent nuclear waste using ionic liquids. Korean J Chem Eng 27: 1360–1365.
  16. 16. Kamavaram V, Reddy RG (2008) Thermal stabilities of di-alkylimidazolium chloride ionic liquids. International Journal of Thermal Sciences 47: 773–777.
  17. 17. Liu X, Zhou F, Liang Y, Liu W (2006) Benzotriazole As The Additive For Ionic Liquid Lubricant: One Pathway Towards Actual Application of Ionic Liquid. Tribology Letters 23: 191–196.
  18. 18. Earle MJ, Seddon KR (2000) Ionic liquids. Green solvents for the future Pure Appl. Chem 72: 1391–1398.
  19. 19. Seddon KR, Stark A, Torres MJ (2000) Influence of chloride, water, and organic solvents on the physical properties of ionic liquids. Pure Appl Chem 72: 2275–2287.
  20. 20. Zhou Y (2005) Recent advances in ionic liquids for synthesis of inorganic nanomaterials. Current Nanoscience 1: 35–42.
  21. 21. Antonietti M, Kuang D, Smarsly B, Zhou Y (2004) Ionic Liquids for the Convenient Synthesis of Functional Nanoparticles and Other Inorganic Nanostructures. Angew Chem Int Ed 43: 4988–4992.
  22. 22. Kim KS, Demberelnyamba ND, Yeon S, Choi S, Cha J, et al. (2005) One-Phase Preparation of Palladium Nanoparticles Using Thiol-Functionalized Ionic Liquid. Korean J Chem Eng 22: 717–720.
  23. 23. Wang L, Zhao B, Yuan ZY, Zhang XJ, Wu QD (2007) Sci China Ser B-Chem. 53. : 63–69.
    • 24. Dewan M, Kumar A, Saxena A, De A, Mozumdar S (2010) Molecular iodine in [bmim][BF4]: a highly efficient green catalytic system for one-pot synthesis of 1,3-oxathiolan-5-one. Tetrahedron Letters 51: 6108–6110.
    • 25. Kumar A, Singh P, Saxena A, De A, Chandra R, et al. (2008) Cu- nanoparticles – an efficient catalyst for one pot three component synthesis of Thiazolidine-2,4-dione derivatives. Catalysis Communications 10: 17–22.
    • 26. Kumar A, Dewan M, Saxena A, De A, Mozumdar S (2010) Knoevenagel condensation catalyzed by chemo-selective Ni-nanoparticles in neutral medium. Catalysis Communications 11: 679–683.
    • 27. Kumar A, Kumar S, Saxena A, De A, Mozumdar S (2008) Ni-Nanoparticles: An Efficient Catalyst for the Synthesis of Quinoxalines. Catalysis Communications, 9: 778–784.
    • 28. Kumar A, Kumar S, Saxena A, De A, Mozumdar S (2008) Selective Protection of Carbonyl Compounds over Nano-Sized Nickel Catalysts. Catalysis Letters 122: 98–105.
    • 29. Kumar A, Saxena A, Dewan M, De A, Mozumdar S (2011) Recyclable nanoparticulate copper mediated synthesis of naphthoxazinones in PEG-400: a green approach. Tetrahedron Letters 38: 4835–4839.
    • 30. Jin K, Huang X, Pang L, Li J, Appel A, et al. (2002) Cu(I)(bpp)]BF4: the first extended coordination network prepared solvothermally in an ionic liquid solvent. ChemComm 23: 2872–2873.