Staging research of human lung cancer tissues by high-resolution magic angle spinning proton nuclear magnetic resonance spectroscopy (HRMAS 1 H NMR) and multivariate data analysis

2016 ◽  
Vol 13 (5) ◽  
pp. e232-e238 ◽  
Author(s):  
Wenxue Chen ◽  
Shaohua Lu ◽  
Guifang Wang ◽  
Fener Chen ◽  
Chunxue Bai
Keyword(s):  
Multivariate Data Analysis ◽  
Human Lung ◽  
Magic Angle Spinning ◽  
Proton Nuclear Magnetic Resonance ◽  
Human Lung Cancer ◽  
Resonance Spectroscopy ◽  
Magic Angle ◽  
H Nmr ◽  
Angle Spinning ◽  
Cancer Tissues

Metabolic Profiling of Human Lung Cancer Tissue by1H High Resolution Magic Angle Spinning (HRMAS) NMR Spectroscopy

2010 ◽  
Vol 9 (1) ◽  
pp. 319-332 ◽  
Author(s):  
Cláudia M. Rocha ◽  
António S. Barros ◽  
Ana M. Gil ◽  
Brian J. Goodfellow ◽  
Eberhard Humpfer ◽  
...  
Keyword(s):  
Metabolic Profiling ◽  
Human Lung ◽  
Magic Angle Spinning ◽  
Human Lung Cancer ◽  
Cancer Tissue ◽  
Magic Angle ◽  
Lung Cancer Tissue ◽  
Hrmas Nmr ◽  
Angle Spinning ◽  
Human Lung Cancer Tissue

scholarly journals Preparation of Li3PS4–Li3PO4 Solid Electrolytes by Liquid-Phase Shaking for All-Solid-State Batteries

2021 ◽  
Vol 2 (1) ◽  
pp. 39-48
Author(s):  
Nguyen H. H. Phuc ◽  
Takaki Maeda ◽  
Tokoharu Yamamoto ◽  
Hiroyuki Muto ◽  
Atsunori Matsuda
Keyword(s):  
Solid Solution ◽  
Solid State ◽  
Liquid Phase ◽  
Room Temperature ◽  
Reaction Medium ◽  
Magic Angle Spinning ◽  
Resonance Spectroscopy ◽  
Synthesis Methods ◽  
Magic Angle ◽  
Angle Spinning

A solid solution of a 100Li3PS4·xLi3PO4 solid electrolyte was easily prepared by liquid-phase synthesis. Instead of the conventional solid-state synthesis methods, ethyl propionate was used as the reaction medium. The initial stage of the reaction among Li2S, P2S5 and Li3PO4 was proved by ultraviolet-visible spectroscopy. The powder X-ray diffraction (XRD) results showed that the solid solution was formed up to x = 6. At x = 20, XRD peaks of Li3PO4 were detected in the prepared sample after heat treatment at 170 °C. However, the samples obtained at room temperature showed no evidence of Li3PO4 remaining for x = 20. Solid phosphorus-31 magic angle spinning nuclear magnetic resonance spectroscopy results proved the formation of a POS33− unit in the sample with x = 6. Improvements of ionic conductivity at room temperature and activation energy were obtained with the formation of the solid solution. The sample with x = 6 exhibited a better stability against Li metal than that with x = 0. The all-solid-state half-cell employing the sample with x = 6 at the positive electrode exhibited a better charge–discharge capacity than that employing the sample with x = 0.

Leucite-pollucite structure-type variability and the structure of a synthetic end-member calcium wairakite (CaAl2Si4O12·2H2O)

1998 ◽  
Vol 62 (2) ◽  
pp. 165-178 ◽  
Author(s):  
C. M. B. Henderson ◽  
A. M. T. Bell ◽  
S. C. Kohn ◽  
C. S. Page
Keyword(s):  
Rietveld Analysis ◽  
Structure Type ◽  
Magic Angle Spinning ◽  
Resonance Spectroscopy ◽  
Magic Angle ◽  
Synthetic Sample ◽  
Cation Site ◽  
Wide Range ◽  
Angle Spinning ◽  
Cation Sites

AbstractThe structure of a synthetic end-member wairakite (CaAl2Si4O12·2H2O) has been determined using Rietveld analysis of high-resolution, synchrotron X-ray powder diffraction data, and 29Si and 27Al magic angle spinning nuclear magnetic resonance spectroscopy. The framework in the synthetic sample is more disordered than that in natural wairakite. Ca is distributed over the cavity cation sites M2, M12A, M12B in the approximate proportions 0.8:0.1:0.1, respectively, with M11 being vacant. 29Si MAS NMR data are consistent with about 80% of the Si occupying tetrahedral T11 and T12 sites linked to two Al atoms [Q4(2Al) silicons]. Tetrahedral and cavity cation site disorder are coupled so that Al mainly occupies T2 sites, with Ca in M12A and M12B being balanced by Al in T12A and T12B; T11A and T11B sites appear to only contain Si, in agreement with the M11 site being vacant. The crystal chemistries of the wide range of stoichiometries which crystallize with the leucite/pollucite structure-type are also reviewed, with particular attention being paid to the tetrahedral ordering configurations present in these phases, and the implications to crystallographic phase transitions.

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