The presence of CsI in nuclear fuel has long been debated. Its formation significantly decreases volatility, thereby reducing the rate at which iodine and cesium are released from the reactor core during a nuclear accident. A series of samples were investigated by Knudsen Effusion Mass Spectrometry (KEMS) in order to determine whether CsI is present in irradiated nuclear fuel. The examined samples were pure CsI, CsI exposed to gamma radiation, CsI-doped UO2 simulated fuel and irradiated LWR fuel samples. The CsI and CsI-doped samples were examined to establish boundary conditions for the detection of CsI by KEMS. These samples indicated that the presence of CsI in fuel is characterized by three mass spectrometric signals Cs+, I+ and CsI+, with a peak ratio of CsI+ and I+ of 1:0.7. The examinations of irradiated fuels showed none of these characteristics and hence no evidence that CsI is present in irradiated LWR nuclear fuel, at least after a storage period of years.

A new double neptunium zirconium phosphate of the type MxZr2(PO4)3 (M = Np), crystallizing in the structure type NaZr2(PO4)3 (NZP, NASICON), was synthesized by solid state reactions at high temperatures and characterized by X-ray diffraction, infrared spectroscopy and Mössbauer spectroscopy. The Rietveld refinement of the XRD pattern together with the analysis of the IR spectra of the sample confirmed the space group P[3 with combining macron]c, the same as that for the lanthanide analogues Ln0.33Zr2(PO4)3. However, Mössbauer studies revealed the presence of neptunium in the two oxidation states +3 and +4, indicating a two-phase NZP system with different crystallographic environments of the neptunium atoms. The thermal behaviour of the sample was followed up to 1400 °C by thermogravimetric analysis.