Fast neutron surface strain scanning with high spatial resolution

Neutron reflectivity is a powerful technique for characterizing interfaces in many areas of science. The traditional method of time of flight for measuring the wavelength of neutrons in a white beam is extremely wasteful, as the vast majority of neutrons must be absorbed in the choppers in order to produce a pulsed beam. A prism operates continuously, with a transmission up to two orders of magnitude higher than choppers. The wavelength-dependent deflection of the beam by the prism, coupled with a high spatial resolution detector, results in excellent wavelength resolution. The theory of how the resolution is considerably enhanced by curving the surface of the prism is described in detail for a real experimental arrangement. It is demonstrated how this can be used for faster neutron reflectometry, including the merging of different angles and subtraction of background. The technique shows considerable promise for neutron reflectivity, opening up new areas of science particularly in the realms of kinetics and small samples.

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High spatial resolution AEM observations of yttrium segregation in chromia scales grown on Co-45%Cr

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100144103 ◽

1986 ◽

Vol 44 ◽

pp. 518-519

Author(s):

K. Przybylski ◽

A. J. Garratt-Reed ◽

G. J. Yurek

Keyword(s):

Spatial Resolution ◽

Outer Surface ◽

Maximum Concentration ◽

High Spatial Resolution ◽

Reactive Elements ◽

Chromia Scales

The addition of so-called “reactive” elements such as yttrium to alloys is known to enhance the protective nature of Cr2O3 or Al2O3 scales. However, the mechanism by which this enhancement is achieved remains unclear. An A.E.M. study has been performed of scales grown at 1000°C for 25 hr. in pure O2 on Co-45%Cr implanted at 70 keV with 2x1016 atoms/cm2 of yttrium. In the unoxidized alloys it was calculated that the maximum concentration of Y was 13.9 wt% at a depth of about 17 nm. SIMS results showed that in the scale the yttrium remained near the outer surface.

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Integration of Core-Edge Spectroscopy Methods for the Study of Polymers

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s042482010016323x ◽

1996 ◽

Vol 54 ◽

pp. 154-155

Author(s):

E. G. Rightor

Keyword(s):

Excited State ◽

Polymer Blends ◽

Gas Phase ◽

Spatial Resolution ◽

High Spatial Resolution ◽

Electronic States ◽

Core Electron ◽

Bulk Solids ◽

Development Application

Core edge spectroscopy methods are versatile tools for investigating a wide variety of materials. They can be used to probe the electronic states of materials in bulk solids, on surfaces, or in the gas phase. This family of methods involves promoting an inner shell (core) electron to an excited state and recording either the primary excitation or secondary decay of the excited state. The techniques are complimentary and have different strengths and limitations for studying challenging aspects of materials. The need to identify components in polymers or polymer blends at high spatial resolution has driven development, application, and integration of results from several of these methods.

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