I am using a Bruker 600M solid-state NMR spectrometer with a Micro 2.5 microimaging system. The test sample is a tube of 1M LiCl aqueous solution, and the nucleus detected is 1H. I am trying to use this sample to debug the UTE pulse. However, in the actual sampling process, the results obtained with UTE often have very strange artifacts. Since the ParaVision manual provides only very limited content, I would like to know the following:

  • How does the UTE pulse achieve a lower echo time?
  • What are the common artifacts of the UTE pulse, and how can they be avoided?
  • What situations are UTE pulses generally used for? How should the parameters be set? Thank you for your help!
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