Dehydration phase transitions in new aluminium arsenate minerals from the Penberthy Croft mine, Cornwall, UK

2016 ◽  
Vol 80 (7) ◽  
pp. 1205-1217 ◽  
Author(s):  
Ian E. Grey ◽  
Helen E. A. Brand ◽  
John Betterton

AbstractBettertonite, [Al6(AsO4)3(OH)9(H2O)5]•11H2O and penberthycroftite, [Al6(AsO4)3(OH)9(H2O)5].8H2O, two new minerals from the Penberthy Croft mine, Cornwall, have flexible layer structures based on corner-connected heteropolyhedral columns. Their response to dehydration on heating was studied using in situ synchrotron powder X-ray diffraction at temperatures in the range -53 to 157°C. The bettertonite sample transforms to penberthycroftite in a narrow temperature range of 67 to 97°C with a large (8%) contraction of the layer separation and a 6 Å sliding of adjacent layers relative to each other. Above 100°C a second phase transition occurs to a DL (displaced layer) phase, involving another 8% inter-layer contraction combined with a rotation of the columns. On heating the penberthycroftite sample the phase transition to the DL phase occurs at a lower temperature of ∼80°C. The DL phase is stable to a temperature of ∼120°C. At higher temperatures, increased rotation of the columns is accompanied by a progressive amorphization of the sample. Bettertonite, penberthycroftite and the DL phase exhibit negative thermal expansion (NTE) along all three axes with large NTE coefficients, of the order of-100 x 10 -6 °C-1.

Author(s):  
Rebecca Scatena ◽  
Michał Andrzejewski ◽  
Roger D Johnson ◽  
Piero Macchi

Through in-situ, high-pressure x-ray diffraction experiments we have shown that the homoleptic perovskite-like coordination polymer [(CH3)2NH2]Cu(HCOO)3 undergoes a pressure-induced orbital reordering phase transition above 5.20 GPa. This transition is distinct...


2010 ◽  
Vol 504 ◽  
pp. S155-S158 ◽  
Author(s):  
J. Bednarcik ◽  
C. Curfs ◽  
M. Sikorski ◽  
H. Franz ◽  
J.Z. Jiang

2021 ◽  
Vol 118 (13) ◽  
pp. 132903
Author(s):  
Mao-Hua Zhang ◽  
Changhao Zhao ◽  
Lovro Fulanović ◽  
Jürgen Rödel ◽  
Nikola Novak ◽  
...  

2020 ◽  
Vol 12 (9) ◽  
pp. 1409-1412
Author(s):  
Jeong-Tae Moon ◽  
Tae-Hyun Nam

The effect of annealing temperature and external stress on the thermal expansion of a Ti–23Nb–0.7Ta–2Zr alloy were investigated by means of thermal expansion tests under constant load and X-ray diffraction (XRD). Negative thermal expansion (NTE), which is a shrinkage during heating, was observed in both a cold rolled and annealed specimens. The intensity of (200)β peak decreased while that of (211)β peak increased as the annealing temperature increased. The difference in expansion rate between 50 °C and 250 °C is found to decrease with an increasing annealing temperature from 600 °C to 800 °C, above which it kept almost constant. The expansion rate decreased as the applied stress increased.


2021 ◽  
Author(s):  
Jinsheng Liao ◽  
Minghua Wang ◽  
Fulin Lin ◽  
Zhuo Han ◽  
Datao Tu ◽  
...  

Abstract Lanthanide (Ln3+)-doped phosphors generally suffer from thermal quenching, in which their photoluminescence (PL) intensities decrease at the higher temperature. Herein, we report a class of unique two-dimensional negative-thermal-expansion phosphor of Sc2(MoO4)3:Yb/Er. By virtue of the reduced distances between sensitizers and emitters as well as confined energy migration with increasing the temperature, a 45-fold enhancement of green upconversion (UC) luminescence and a 450-fold enhancement of near-infrared downshifting (DS) luminescence of Er3+ are achieved from 25 to 500 ˚C. The thermally boosted UC and DS luminescence mechanism is systematically investigated through in situ temperature-dependent Raman spectroscopy, synchrotron X-ray diffraction and PL dynamics. Moreover, the luminescence lifetime of 4I11/2 of Er3+ in Sc2(MoO4)3:Yb/Er displays a strong temperature dependence, enabling ratiometric thermometry with the highest relative sensitivity of 13.4%/K at 298 K. These findings may gain a vital insight into the design of negative-thermal-expansion Ln3+-doped phosphors for versatile applications.


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