Possibilities and limitations of different analytical methods for the size determination of a bimodal dispersion of metallic nanoparticles

被引:157
作者
Mahl, Dirk [1 ]
Diendorf, Joerg [1 ]
Meyer-Zaika, Wolfgang [1 ]
Epple, Matthias [1 ]
机构
[1] Univ Duisburg Essen, Ctr Nanointegrat Duisburg Essen CeNIDE, D-45117 Essen, Germany
关键词
Nanoparticles; Electron microscopy; Dynamic light scattering; Analytical disc centrifugation; Nanoparticle tracking analysis; Particle size analysis; DYNAMIC LIGHT-SCATTERING; PARTICLE-SIZE; ANALYTICAL ULTRACENTRIFUGATION; SILVER NANOPARTICLES; GOLD NANOPARTICLES; CYTOTOXICITY; NANOMATERIALS; TOXICITY; CLUSTERS;
D O I
10.1016/j.colsurfa.2011.01.031
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Silver nanoparticles (about 70 nm) and gold nanoparticles (about 15 nm) were prepared and colloidally stabilized with poly(vinylpyrrolidone) (PVP). The pure nanoparticles as well as a 1:1 mixture (w:w) were analysed with a variety of methods which probe the size distribution: Scanning electron microscopy, transmission electron microscopy, dynamic light scattering, analytical disc centrifugation, and Brownian motion analysis (nanoparticle tracking analysis). The differences between the methods are highlighted and their ability to distinguish between silver and gold nanoparticles in the mixture is demonstrated. The size distribution data from the different methods were clearly different, therefore it is recommended to apply more than one method to characterize the nanoparticle dispersion. In particular, the smaller particles were undetectable by dynamic light scattering and nanoparticle tracking analysis in the presence of the large particles. For the 1:1 mixture, only electron microscopy and analytical disc centrifugation were able to give quantitative data on the size distribution. On the other hand, it is not possible to make statements about an agglomeration in dispersion with electron microscopy because an agglomeration may also have occurred during the drying process. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:386 / 392
页数:7
相关论文
共 30 条
[1]   The size distribution of 'gold standard' nanoparticles [J].
Bienert, Ralf ;
Emmerling, Franziska ;
Thuenemann, Andreas F. .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2009, 395 (06) :1651-1660
[2]   Comparison of scanning electron microscopy, dynamic light scattering and analytical ultracentrifugation for the sizing of poly(butyl cyanoacrylate) nanoparticles [J].
Bootz, A ;
Vogel, V ;
Schubert, D ;
Kreuter, J .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2004, 57 (02) :369-375
[3]   Particle size distribution measurement from millimeters to nanometers, and from rods to platelets [J].
Bowen, P .
JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY, 2002, 23 (05) :631-662
[4]   Human-related application and nanotoxicology of inorganic particles: complementary aspects [J].
Choi, Soo-Jin ;
Oh, Jae-Min ;
Choy, Jin-Ho .
JOURNAL OF MATERIALS CHEMISTRY, 2008, 18 (06) :615-620
[5]   Particle size distributions of silver nanoparticles at environmentally relevant conditions [J].
Cumberland, Susan A. ;
Lead, Jamie R. .
JOURNAL OF CHROMATOGRAPHY A, 2009, 1216 (52) :9099-9105
[6]   Particle Size Distribution Measurements of Manganese-Doped ZnS Nanoparticles [J].
Dieckmann, Yvonne ;
Coelfen, Helmut ;
Hofmann, Heinrich ;
Petri-Fink, Alke .
ANALYTICAL CHEMISTRY, 2009, 81 (10) :3889-3895
[7]   On the role of block copolymer additives for calcium carbonate crystallization:: Small angle neutron scattering investigation by applying contrast variation [J].
Endo, H ;
Schwahn, D ;
Cölfen, H .
JOURNAL OF CHEMICAL PHYSICS, 2004, 120 (19) :9410-9423
[8]   Stable Prenucleation Calcium Carbonate Clusters [J].
Gebauer, Denis ;
Voelkel, Antje ;
Coelfen, Helmut .
SCIENCE, 2008, 322 (5909) :1819-1822
[9]   Gold Nanoparticles for Biology and Medicine [J].
Giljohann, David A. ;
Seferos, Dwight S. ;
Daniel, Weston L. ;
Massich, Matthew D. ;
Patel, Pinal C. ;
Mirkin, Chad A. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (19) :3280-3294
[10]   Nanobiomaterials and nanoanalysis: Opportunities for improving the science to benefit biomedical technologies [J].
Grainger, David W. ;
Castner, David G. .
ADVANCED MATERIALS, 2008, 20 (05) :867-877