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Nanocrystalline and stacking-disordered β -cristobalite AlPO 4 chemically stabilized at room temperature: synthesis, physical characterization, and X-ray powder diffraction data
This paper reports the first successful synthesis and the structural characterization of nanocrystalline and stacking-disordered β -cristobalite AlPO 4 that is chemically stabilized down to room temperature and free of crystalline impurity phases. Several batches of the title compound were synthesiz...
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Published in: | Powder diffraction 2017-09, Vol.32 (S1), p.S193-S200 |
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container_issue | S1 |
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container_title | Powder diffraction |
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creator | Peplinski, B. Adamczyk, B. Formanek, P. Meyer, C. Krüger, O. Scharf, H. Reinsch, S. Ostermann, M. Nofz, M. Jäger, C. Adam, C. Emmerling, F. |
description | This paper reports the first successful synthesis and the structural characterization of nanocrystalline and stacking-disordered
β
-cristobalite AlPO
4
that is chemically stabilized down to room temperature and free of crystalline impurity phases. Several batches of the title compound were synthesized and thoroughly characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy, selected area electron diffraction, energy dispersive X-ray spectroscopy mapping in SEM, solid-state
31
P nuclear magnetic resonance (
31
P-NMR) spectroscopy including the TRAPDOR method, differential thermal analysis (DTA), gas-sorption methods, optical emission spectroscopy, X-ray fluorescence spectroscopy, and ion chromatography. Parameters that are critical for the synthesis were identified and optimized. The synthesis procedure yields reproducible results and is well documented. A high-quality XRD pattern of the title compound is presented, which was collected with monochromatic copper radiation at room temperature in a wide 2
θ
range of 5°–100°. |
doi_str_mv | 10.1017/S0885715617000537 |
format | article |
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β
-cristobalite AlPO
4
that is chemically stabilized down to room temperature and free of crystalline impurity phases. Several batches of the title compound were synthesized and thoroughly characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy, selected area electron diffraction, energy dispersive X-ray spectroscopy mapping in SEM, solid-state
31
P nuclear magnetic resonance (
31
P-NMR) spectroscopy including the TRAPDOR method, differential thermal analysis (DTA), gas-sorption methods, optical emission spectroscopy, X-ray fluorescence spectroscopy, and ion chromatography. Parameters that are critical for the synthesis were identified and optimized. The synthesis procedure yields reproducible results and is well documented. A high-quality XRD pattern of the title compound is presented, which was collected with monochromatic copper radiation at room temperature in a wide 2
θ
range of 5°–100°.</description><identifier>ISSN: 0885-7156</identifier><identifier>EISSN: 1945-7413</identifier><identifier>DOI: 10.1017/S0885715617000537</identifier><language>eng</language><ispartof>Powder diffraction, 2017-09, Vol.32 (S1), p.S193-S200</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-crossref_primary_10_1017_S08857156170005373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Peplinski, B.</creatorcontrib><creatorcontrib>Adamczyk, B.</creatorcontrib><creatorcontrib>Formanek, P.</creatorcontrib><creatorcontrib>Meyer, C.</creatorcontrib><creatorcontrib>Krüger, O.</creatorcontrib><creatorcontrib>Scharf, H.</creatorcontrib><creatorcontrib>Reinsch, S.</creatorcontrib><creatorcontrib>Ostermann, M.</creatorcontrib><creatorcontrib>Nofz, M.</creatorcontrib><creatorcontrib>Jäger, C.</creatorcontrib><creatorcontrib>Adam, C.</creatorcontrib><creatorcontrib>Emmerling, F.</creatorcontrib><title>Nanocrystalline and stacking-disordered β -cristobalite AlPO 4 chemically stabilized at room temperature: synthesis, physical characterization, and X-ray powder diffraction data</title><title>Powder diffraction</title><description>This paper reports the first successful synthesis and the structural characterization of nanocrystalline and stacking-disordered
β
-cristobalite AlPO
4
that is chemically stabilized down to room temperature and free of crystalline impurity phases. Several batches of the title compound were synthesized and thoroughly characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy, selected area electron diffraction, energy dispersive X-ray spectroscopy mapping in SEM, solid-state
31
P nuclear magnetic resonance (
31
P-NMR) spectroscopy including the TRAPDOR method, differential thermal analysis (DTA), gas-sorption methods, optical emission spectroscopy, X-ray fluorescence spectroscopy, and ion chromatography. Parameters that are critical for the synthesis were identified and optimized. The synthesis procedure yields reproducible results and is well documented. A high-quality XRD pattern of the title compound is presented, which was collected with monochromatic copper radiation at room temperature in a wide 2
θ
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β
-cristobalite AlPO
4
that is chemically stabilized down to room temperature and free of crystalline impurity phases. Several batches of the title compound were synthesized and thoroughly characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy, selected area electron diffraction, energy dispersive X-ray spectroscopy mapping in SEM, solid-state
31
P nuclear magnetic resonance (
31
P-NMR) spectroscopy including the TRAPDOR method, differential thermal analysis (DTA), gas-sorption methods, optical emission spectroscopy, X-ray fluorescence spectroscopy, and ion chromatography. Parameters that are critical for the synthesis were identified and optimized. The synthesis procedure yields reproducible results and is well documented. A high-quality XRD pattern of the title compound is presented, which was collected with monochromatic copper radiation at room temperature in a wide 2
θ
range of 5°–100°.</abstract><doi>10.1017/S0885715617000537</doi></addata></record> |
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source | Cambridge Journals Online |
title | Nanocrystalline and stacking-disordered β -cristobalite AlPO 4 chemically stabilized at room temperature: synthesis, physical characterization, and X-ray powder diffraction data |
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