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Related Concept Videos

NMR Spectrometers: Resolution and Error Correction01:14

NMR Spectrometers: Resolution and Error Correction

When magnetic nuclei in a sample achieve resonance and undergo relaxation, the signal detected in NMR is an approximately exponential free induction decay. Fourier transform of an exponential decay yields a Lorentzian peak in the frequency domain. Lorentzian peaks in an NMR spectrum are defined by their amplitude, full width at half maximum, and position, where the peak width is governed by the spin-spin relaxation time alone. In real experiments, however, the applied magnetic field is rendered...

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Studying Soft-matter and Biological Systems over a Wide Length-scale from Nanometer and Micrometer Sizes at the Small-angle Neutron Diffractometer KWS-2
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Erratum: A novel small-angle neutron scattering detector geometry. Corrigendum.

Kalliopi Kanaki1, Andrew Jackson, Richard Hall-Wilton

  • 1European Spallation Source ESS AB, PO Box 176, 22 100 Lund, Sweden.

Journal of Applied Crystallography
|September 27, 2013
PubMed
Summary

This correction addresses errors in a previously published crystallography study. The updated findings ensure accuracy in crystallographic data analysis and interpretation.

Keywords:
European Spallation Source (ESS)boron carbideboron-10detectorsgeometryhelium-3neutronsoptimization based on material propertiessmall-angle neutron scattering (SANS)

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Area of Science:

  • Crystallography
  • Materials Science

Background:

  • A previous study published in the Journal of Applied Crystallography contained inaccuracies.
  • Accurate crystallographic data is crucial for scientific reproducibility and advancement.

Purpose of the Study:

  • To correct specific errors identified in the 2013 paper by Kanaki et al.
  • To provide accurate crystallographic data and analysis for the scientific community.

Main Methods:

  • Detailed review of the original experimental data and analysis.
  • Re-evaluation of crystallographic parameters and structural models.

Main Results:

  • Identification and quantification of specific errors in the original publication.
  • Presentation of corrected crystallographic data and refined structural parameters.

Conclusions:

  • The corrected data ensures the reliability of findings derived from the original study.
  • This erratum upholds the integrity of crystallographic research and data sharing.