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Frontiers of Environmental Science & Engineering

ISSN 2095-2201

ISSN 2095-221X(Online)

CN 10-1013/X

Postal Subscription Code 80-973

2018 Impact Factor: 3.883

Front. Environ. Sci. Eng.    2015, Vol. 9 Issue (2) : 197-205    https://doi.org/10.1007/s11783-014-0624-6
RESEARCH ARTICLE
Behavior of aqueous stable colloidal nano-C60 aggregates exposed to TX100 micelles under different environmental conditions
Jing HUO,Ye YU,Ling GE,Bo ZHANG(),Yiliang HE
School of Environmental Science & Engineering, Shanghai Jiaotong University, Shanghai 200240, China
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Abstract

C60, as one of carbon nanomaterials widely used in various fields, could be released into the water environment thus exerting some potential health risks to human beings. This work examined the behavior of aqueous stable colloidal nano-C60 (nC60) aggregates under different environmental conditions including Polyethylene glycol octylphenol ether (TX100) micelles concentration, pH, and reaction time when exposed to TX100 micelles. Results show that the nC60 aggregates became more dispersive and restored the capability of generating the singlet oxygen when exposed to TX100 micelles. With the increase of TX100 concentration, smaller average size of nC60 aggregates was observed in dynamic light scattering (DLS) analysis, the fluorescence intensity of TX100 was more quenched by nC60 aggregates, and the kinetic rate constant of generating the singlet oxygen for nC60 aggregates was improved. The mean size of nC60 aggregates in the presence of TX100 had no obvious variations when the pH ranged from 4 to 8. The longer reaction time between nC60 aggregates and TX100 led to a higher kinetic rate constant of generating the singlet oxygen. Collective data suggest that variations in physicochemical properties of nC60 aggregates are strongly dependent on the surrounding media under different environmental conditions and directly govern nC60’s transport behavior and potential toxicity.

Keywords nano-C60 (nC60) aggregates      photochemical reactivity      artificial biological membrane     
Corresponding Author(s): Bo ZHANG   
Online First Date: 03 January 2014    Issue Date: 13 February 2015
 Cite this article:   
Jing HUO,Ye YU,Ling GE, et al. Behavior of aqueous stable colloidal nano-C60 aggregates exposed to TX100 micelles under different environmental conditions[J]. Front. Environ. Sci. Eng., 2015, 9(2): 197-205.
 URL:  
https://academic.hep.com.cn/fese/EN/10.1007/s11783-014-0624-6
https://academic.hep.com.cn/fese/EN/Y2015/V9/I2/197
sample TX100 concentration/(g·L-1) stirring time/h pH value stirring intensity/(r·min-1)
1 0.10 24 unadjusted 600
2 5.00 24 unadjusted 600
3 10.00 24 unadjusted 600
4 25.00 24 unadjusted 600
5 50.00 24 unadjusted 600
6 50.00 0 unadjusted 600
7 50.00 3 unadjusted 600
8 50.00 6 unadjusted 600
9 50.00 9 unadjusted 600
10 50.00 24 4 600
11 50.00 24 5 600
12 50.00 24 6 600
13 50.00 24 7 600
14 50.00 24 8 600
Tab.1  Preparation of TX100/nC60 samples
Fig.1  Characterization of nC60 aggregates in the absence of TX100 by DLS and TEM: a) DLS characterization of nC60; b) effect of pH on Z-average diameters (Z-ave) of nC60 sample; c) TEM images of nC60 aggregates
Fig.2  DLS analysis of nC60 samples after mixing with solution containing TX100 of different concentrations: a)<CMC; b)>CMC (All samples were magnetically stirred at 600 r·min-1 for 24 h)
Fig.3  Fluorescence intensity analysis of TX100 mixed with nC60 samples: a) fluorescence intensity of TX100 in the presence of nC60 (5 mg·L-1); b) reduced TX100 fluorescence intensity by nC60 at different concentration of TX100 (All samples were magnetically stirred at 600 r·min-1 for 24 h)
Fig.4  Photochemical reactivity of nC60 aggregates after mixing with solution containing TX100 of different concentrations: a) degradation rate of FFA; b) kinetic rate constant of FFA degradation (All samples were magnetically stirred at 600 r·min-1 for 24 h)
Fig.5  DLS analysis of nC60 aggregates after mixing 50.00 g·L-1 TX100 at different pH (All samples were magnetically stirred at 600 r·min-1 for 24 h)
Fig.6  Photochemical reactivity of nC60 aggregates after mixing 50.00 g·L-1 TX100 at different pH: a) degradation rate of FFA; b) kinetic rate constant of FFA degradation (All samples were magnetically stirred at 600 r·min-1 for 24 h)
Fig.7  Fluorescence analysis of nC60 aggregates after mixing 50.00 g·L-1 TX100 for different periods of time (All samples were magnetically stirred at 600 r·min-1)
Fig.8  Photochemical reactivity of nC60 aggregates after mixing 50.00 g·L-1 TX100 for different periods of time: (a) degradation rate of FFA; (b) kinetic rate constant of FFA degradation (All samples were magnetically stirred at 600 r·min-1)
1 Lens M. Recent progresses in application of fullerenes in cosmetics. Recent Patents on Biotechnology, 2011, 5(2): 67–73
https://doi.org/10.2174/187220811796365707 pmid: 21619548
2 Lin C M, Lu T Y. C60 fullerene derivatized nanoparticles and their application to therapeutics. Recent Patents on Nanotechnology, 2012, 6(2): 105–113
https://doi.org/10.2174/187221012800270135 pmid: 22455733
3 Nierengarten J F. Chemical modification of C60 for materials science applications. New Journal of Chemistry, 2004, 28(10): 1177–1191
https://doi.org/10.1039/b402661f
4 Kroto H W, Allaf A W, Balm S P. C60: buckminsterfullerene. Chemical Reviews, 1991, 91(6): 1213–1235
https://doi.org/10.1021/cr00006a005
5 Jafvert C T, Kulkarni P P. Buckminsterfullerene’s (C60) octanol-water partition coefficient (Kow) and aqueous solubility. Environmental Science & Technology, 2008, 42(16): 5945–5950
https://doi.org/10.1021/es702809a pmid: 18767649
6 Fortner J D, Lyon D Y, Sayes C M, Boyd A M, Falkner J C, Hotze E M, Alemany L B, Tao Y J, Guo W, Ausman K D, Colvin V L, Hughes J B. C60 in water: nanocrystal formation and microbial response. Environmental Science & Technology, 2005, 39(11): 4307–4316
https://doi.org/10.1021/es048099n pmid: 15984814
7 Sayes C M, Fortner J D, Guo W, Lyon D, Boyd A M, Ausman K D, Tao Y J, Sitharaman B, Wilson L J, Hughes J B, West J L, Colvin V L. The differential cytotoxicity of water-soluble fullerenes. Nano Letters, 2004, 4(10): 1881–1887
https://doi.org/10.1021/nl0489586
8 Song M, Yuan S, Yin J, Wang X, Meng Z, Wang H, Jiang G. Size-dependent toxicity of nano-C60 aggregates: more sensitive indication by apoptosis-related Bax translocation in cultured human cells. Environmental Science & Technology, 2012, 46(6): 3457–3464
https://doi.org/10.1021/es2039008 pmid: 22352688
9 Lee J, Fortner J D, Hughes J B, Kim J H. Photochemical production of reactive oxygen species by C60 in the aqueous phase during UV irradiation. Environmental Science & Technology, 2007, 41(7): 2529–2535
https://doi.org/10.1021/es062066l pmid: 17438811
10 Fortner J D, Lyon D Y, Sayes C M, Boyd A M, Falkner J C, Hotze E M, Alemany L B, Tao Y J, Guo W, Ausman K D, Colvin V L, Hughes J B. C60 in water: nanocrystal formation and microbial response. Environmental Science & Technology, 2005, 39(11): 4307–4316
https://doi.org/10.1021/es048099n pmid: 15984814
11 Brant J, Lecoanet H, Hotze M, Wiesner M. Comparison of electrokinetic properties of colloidal fullerenes (n-C60) formed using two procedures. Environmental Science & Technology, 2005, 39(17): 6343–6351
https://doi.org/10.1021/es050090d pmid: 16190186
12 Xie B, Xu Z H, Guo W H, Li Q L. Impact of natural organic matter on the physicochemical properties of aqueous C60 nanoparticles. Environmental Science & Technology, 2008, 42(8): 2853–2859
https://doi.org/10.1021/es702231g pmid: 18497134
13 Chang X J, Vikesland P J. Effects of carboxylic acids on nC60 aggregate formation. Environmental Pollution, 2009, 157(4): 1072–1080
https://doi.org/10.1016/j.envpol.2008.09.052 pmid: 19054600
14 Chen K L, Elimelech M. Influence of humic acid on the aggregation kinetics of fullerene (C60) nanoparticles in monovalent and divalent electrolyte solutions. Journal of Colloid and Interface Science, 2007, 309(1): 126–134
https://doi.org/10.1016/j.jcis.2007.01.074 pmid: 17331529
15 Hungerbuehler H, Guldi D M, Asmus K D. Incorporation of C60 into artificial lipid membranes. Journal of the American Chemical Society, 1993, 115(8): 3386–3387
https://doi.org/10.1021/ja00061a070
16 Andrievsky G V, Kosevich M V, Vovk M, Shelkovsky V S, Vashchenko L A. On the production of an aqueous colloidal solution of fullerenes. Journal of the Chemical Society. Chemical Communications, 1995, 12(12): 1281–1282
https://doi.org/10.1039/c39950001281
17 Brant J A, Labille J, Bottero J Y, Wiesner M R. Characterizing the impact of preparation method on fullerene cluster structure and chemistry. Langmuir, 2006, 22(8): 3878–3885
https://doi.org/10.1021/la053293o pmid: 16584270
18 Zhang B, Cho M, Hughes J B, Kim J H. Translocation of C60 from aqueous stable colloidal aggregates into surfactant micelles. Environmental Science & Technology, 2009, 43(24): 9124–9129
https://doi.org/10.1021/es9026369 pmid: 19928758
19 Deguchi S, Alargova R G, Tsujii K. Stable dispersions of fullerenes, C60 and C70, in water. Preparation and characterization. Langmuir, 2001, 17(19): 6013–6017
https://doi.org/10.1021/la010651o
20 Mchedlov-Petrossyan N O, Klochkov V K, Andrievsky G V. Colloidal dispersions of fullerene C60 in water: some properties and regularities of coagulation by electrolytes. Journal of the Chemical Society, Faraday Transactions, 1997, 93(24): 4343–4346
https://doi.org/10.1039/a705494g
21 Kumbhakar M, Goel T, Mukherjee T, Pal H. Role of micellar size and hydration on solvation dynamics: a temperature dependent study in Triton-X-100 and Brij-35 micelles. Journal of Physical Chemistry B, 2004, 108(50): 19246–19254
https://doi.org/10.1021/jp0468004
22 Kumbhakar M, Nath S, Mukherjee T, Pal H. Solvation dynamics in triton-X-100 and triton-X-165 micelles: effect of micellar size and hydration. The Journal of Chemical Physics, 2004, 121(12): 6026–6033
https://doi.org/10.1063/1.1784774 pmid: 15367031
23 Behera K, Dahiya P, Pandey S. Effect of added ionic liquid on aqueous Triton X-100 micelles. Journal of Colloid and Interface Science, 2007, 307(1): 235–245
https://doi.org/10.1016/j.jcis.2006.11.009 pmid: 17184790
24 Kumbhakar M, Goel T, Mukherjee T, Pal H. Nature of the water molecules in the palisade layer of a triton X-100 micelle in the presence of added salts: a solvation dynamics study. Journal of Physical Chemistry B, 2005, 109(29): 14168–14174
https://doi.org/10.1021/jp0520291 pmid: 16852779
25 Das P, Mallick A, Purkayastha P, Haldar B, Chattopadhyay N. Fluorescence resonance energy transfer from TX-100 to 3-acetyl-4-oxo-6,7-dihydro-12 H-indolo-[2,3-a] quinolizine in premicellar and micellar environments. Journal of Molecular Liquids, 2007, 130(1–3): 48–51
https://doi.org/10.1016/j.molliq.2006.04.001
26 Haag W R, Hoigne J, Gassman E, Braun A M Singlet oxygen in surface waters-Part I: furfuryl alcohol as a trapping agent. Chemosphere, 1984, 13(5–6): 631–640
https://doi.org/10.1016/0045-6535(84)90199-1
27 Li Y, Zhang W, Niu J F, Chen Y S. Mechanism of photogenerated reactive oxygen species and correlation with the antibacterial properties of engineered metal-oxide nanoparticles. ACS Nano, 2012, 6(6): 5164–5173
https://doi.org/10.1021/nn300934k pmid: 22587225
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