| Ultra
Small
Angle
Neutron
Scattering
(
USANS
) measures the elastic scattering from scattering
length density fluctuations in the order of microns in real space, i.e.
in the momentum transfer range of 2 x 10-5 - 2 x 10-3
Å-1. The techniques of choice for
studying the structure of micron sized particles are electron microscopy,
light scattering and atomic force microscopy. There are however a number
of cases where none of these techniques is applicable. Examples are in
materials of low contrast, opaque materials (for light scattering) or in
magnetic structures. In such cases, neutrons are a unique probe when contrast
enhancement is necessary. Applications can be found in colloid science
(mixtures of particles, strongly correlated colloid crystals, particles
of micron size, silicon
macropore arrays), materials science (filled polymers, cements, microporous
media) and polymer science (constrained systems, emulsion polymerisation).
For this pupose various double crystal diffractometer instruments (Bonse-Hart camera) are available at different research facilities. We operate the USANS instrument at the 250kW TRIGA-MARK-II reactor in Vienna as well as the USANS option of the S18 instrument at the Institut Laue-Langevin in Grenoble, France. The Bonse-Hart camera [1, 2] is a double crystal (or triple axis) spectrometer with two perfect Silicon channel cut crystals as monochromator and analyser mounted in parallel geometry on a vibration isolated optical bench. The Q-dependence of the scattered intensity is measured by rocking the analyser crystal, the sample being placed in between the crystals. The minimal Q is given by the width of the rocking curve. The drawback of the Bonse-Hart arrangement is the large ratio between horizontal and vertical divergence, typically in the range 100 - 1000. Deriving pinhole desmeared absolute intensities requires a careful deconvolution procedure, but solutions exist to deconvolute the data in routine experiments [3-6]. The following picture gives a schematic view of an USANS instrument: |
- Back to: top of page
| Lattice constant | a = 1,246 Å |
| bound coherent scattering length |
|
| Number density of Si | N = 4,99479 . 1028 m-3 |
|
|
|
|
|
| F | = 321/2 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| with a full width at half maximum |
|
|
|
|
|
|
|
|
|
|
|
|
|
References
[1] Bonse U., Hart M., Small-angle X-ray scattering by spherical particles of polystyrene and polyvinyltoluene, Appl. Phys. Lett., 7 (1965) 238.
[2] Bonse U., Hart M., In Small-angle X-ray scattering, H. Brumberger, ed., 121 pp. Gordon & Breach, New York.
[3] Gerber Th., Walter G., Schmidt P.W., Use of the sampling theorem for collimation corrections in small angle X-ray scattering, J. Appl. Cryst., 24 (1991) 278.
[4] Gerber Th., Schmidt P.W., The sampling theorem and small angle X-ray scattering, J. Appl. Cryst., 16 (1983) 581.
[5] Lake J.A., An iterative method of slit-correcting small angle X-ray data, Acta Cryst., 23 (1967) 191.
[6] Strobl G.R., A new method for evaluating slit-smeared small angle X-ray scattering data, Acta Cryst., 26 (1970) 367.
- Back to: top of page