Page 11 - PR 2014 2016 07 Nuclear Science and Technology
P. 11

Nuclear Science and Technology | Progress Report  153





               in different proportions, heated to the melting
               temperatures and cooled with a constant rate
               to produce annealed samples for the study.
               X-ray diffraction data for Rietveld analyses
               were collected at room temperature. Four
               different phases were identified in the system
               xLi W O  - (1-x) La W O  for 0≤ x ≤1, namely
                  2  2  7        2  2  9
               LiLa(WO )2, La W O , Li W O  and Li WO .
                        4     2  2  9   2  2  7      2    4
               In the interval 0< x <1, phase LiLa(WO )
                                                         4 2
               is formed for all values of x. One, two or
               even three of the other phases coexist with
               LiLa(WO )  in shorter intermediate intervals
                       4 2
               of x. The cell parameters of LiLa(WO )  and    Fig 7. A few X-ray diffraction patterns obtained with samples from
                                                    4 2       the system xLi W O  - (1-x)La W O . Pattern for x = 0 corresponds to
                                                                                2
                                                                       2
                                                                                    9
                                                                           7
                                                                                  2
                                                                         2
               the occupation factors of Li, La and O, in this   the phase La W O  and for  x = 1 to Li W O .
                                                                      2  2  9        2  2  7
               phase, were also determined in the analyses.
               In order to complete the study, differential
               thermal analysis (DTA) and scanning electron
               microscopy (SEM) were applied to samples
               and single-crystal fibres grown by micro-
               pulling-down (μ-PD) technique.
               Hydration mechanism in
               Portland cements



               A study of the hydration mechanism in Port-
               land cements has been initiated. The study re-
               sults of a co-operation between the Polytechnic
               School at Sao Paulo University and the Neutron
               Diffraction Laboratory at IPEN. Neutron dif-
               fraction patterns of dry and hydrated Portland
               cement were measured in the high-resolution
               neutron diffractometer Aurora. Hydration was
               done with heavy water (D O) owing to the high
                                       2
               level of incoherent background in the pattern
               if light water is used. Rietveld refinement of
               the deuterated and dry cement samples gave
               as result the presence of several phases in
               different proportions. A list of the phases and
               their weight percentages (Wt. %) refined for the
               deuterated sample is as follows: 35.60 of Alite
               (Ca SiO ), 0.46 Portlandite (CaO D ), 19.60 Belite
                  3   5                     2  2
               (Ca SiO ), 39.90 Calcite (CaCO ), 1.10 Anhydrite
                  2   4                    3
               (CaSO ), 1.20 Tricalcium aluminate (Ca Al O )
                     4                              3  2  6
               and 1.30 Periclase (MgO).
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