Related Experiment Video

Updated: Dec 24, 2025

Quantification of Hydrogen Concentrations in Surface and Interface Layers and Bulk Materials through Depth Profiling with Nuclear Reaction Analysis
14:11

Quantification of Hydrogen Concentrations in Surface and Interface Layers and Bulk Materials through Depth Profiling with Nuclear Reaction Analysis

Published on: March 29, 2016

27.4K

C-S-H Pore Size Characterization Via a Combined Nuclear Magnetic Resonance (NMR)-Scanning Electron Microscopy (SEM)

Christoph Naber1, Florian Kleiner2, Franz Becker1

  • 1GeoZentrum Nordbayern, Mineralogy, University of Erlangen-Nuernberg (FAU), Schlossgarten 5a, 91054 Erlangen, Germany.

Materials (Basel, Switzerland)
|April 16, 2020
PubMed

Keywords:
calcium silicate hydratenuclear magnetic resonance (NMR)pore size distributionscanning electron microscopy (SEM)tricalcium silicate

More Related Videos

Measuring the Spin-Lattice Relaxation Magnetic Field Dependence of Hyperpolarized [1-13C]pyruvate11:57

Measuring the Spin-Lattice Relaxation Magnetic Field Dependence of Hyperpolarized [1-13C]pyruvate

Published on: September 13, 2019

6.9K
Author Spotlight: Exploring Intrinsically Disordered Protein Dynamics Through NMR Relaxation Experiments09:25

Author Spotlight: Exploring Intrinsically Disordered Protein Dynamics Through NMR Relaxation Experiments

Published on: November 1, 2024

2.6K

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...
983