Application of the negative staining technique to both aqueous and organic solvent solutions of polymer particles

被引:59
作者
Harris, JR [1 ]
Roos, C
Djalali, R
Rheingans, O
Maskos, M
Schmidt, M
机构
[1] Univ Mainz, Inst Zool, D-55099 Mainz, Germany
[2] Univ Mainz, Inst Phys Chem, D-55099 Mainz, Germany
关键词
polymer solutions; gold cluster; negative stain; organic solvents; uranyl acetate;
D O I
10.1016/S0968-4328(99)00034-7
中图分类号
TH742 [显微镜];
学科分类号
摘要
Transmission electron microscopy (TEM) imaging of:several different polymers in aqueous and organic solutions using the negative staining technique is demonstrated, to emphasise the possibilities of this specimen preparation technique for polymer science. Negative stains can readily be prepared in both water and organic solvents (e.g. dimethyl formamide (DMF), dimethyl sulfoxide (DMSO) and tetrahydrofurane (THF)). Polymer particle size, size distribution and shape seen in negative stain correlates well with those of unstained materials. The particle surface and smaller particles (e.g. 10-20 nm) are more clearly defined in the presence of a negative stain. The inherent problems of sample overload, anomalous double-sided sample spreading of the sample on the carbon support film and rapid drying of polymer and negative stain from organic solvents, do not prevent the production and selection of satisfactory specimen regions for TEM study. The presence of metallic clusters within polymer particles is not masked by negative stain and assessment of the number of metallic clusters entrapped within the polymer and/or free in the solvent can be readily made. The cationic negative stain, uranyl actetate (UA), is widely used as the stain of choice for polymer solutions, but the anionic negative stains (phosphotungstic acid (PTA) and ammonium molybdate (AM)) have also been successfully employed in this work. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:289 / 298
页数:10
相关论文
共 40 条
[1]   Entropically driven microphase transitions in mixtures of colloidal rods and spheres [J].
Adams, M ;
Dogic, Z ;
Keller, SL ;
Fraden, S .
NATURE, 1998, 393 (6683) :349-352
[2]   Cryo-negative staining [J].
Adrian, M ;
Dubochet, J ;
Fuller, SD ;
Harris, JR .
MICRON, 1998, 29 (2-3) :145-160
[3]   Polymer gels with a micron-sized, layer-like architecture by polymerization in lyotropic cocogem phases [J].
Antonietti, M ;
Goltner, C ;
Hentze, HP .
LANGMUIR, 1998, 14 (10) :2670-2676
[4]   Synthesis and characterization of non spherical gold colloids in block-copolymer micelles [J].
Antonietti, M ;
Thunemann, A ;
Wenz, E .
COLLOID AND POLYMER SCIENCE, 1996, 274 (08) :795-800
[5]   Synthesis of sponge-like polymer dispersions via polymerization of bicontinuous microemulsions [J].
Antonietti, M ;
Hentze, HP .
COLLOID AND POLYMER SCIENCE, 1996, 274 (07) :696-702
[6]   Soluble organosilicon micronetworks with spatially confined reaction sites [J].
Baumann, F ;
Deubzer, B ;
Geck, M ;
Dauth, J ;
Sheiko, S ;
Schmidt, M .
ADVANCED MATERIALS, 1997, 9 (12) :955-&
[7]   Morphology of Vergina star 16-arm block copolymers and scaling behavior of interfacial area with graft point functionality [J].
Beyer, FL ;
Gido, SP ;
Poulos, Y ;
Avgeropoulos, A ;
Hadjichristidis, N .
MACROMOLECULES, 1997, 30 (08) :2373-2376
[8]  
BRENNER S, 1959, BIOCHIM BIOPHYS ACTA, V34, P60
[9]   Nanoengineering of inorganic and hybrid hollow spheres by colloidal templating [J].
Caruso, F ;
Caruso, RA ;
Möhwald, H .
SCIENCE, 1998, 282 (5391) :1111-1114
[10]   Helical superstructures from charged poly(styrene)-poly(isocyanodipeptide) block copolymers [J].
Cornelissen, JJLM ;
Fischer, M ;
Sommerdijk, NAJM ;
Nolte, RJM .
SCIENCE, 1998, 280 (5368) :1427-1430