scholarly journals Raman Spectral Changes of Sugi Bark during Thermal Degradation and Carbonization

2000 ◽  
Vol 49 (9Appendix) ◽  
pp. 227-228
Author(s):  
Shigeru YAMAUCHI ◽  
Yoshinari KIKUCHI ◽  
Yasuji KURIMOTO
2005 ◽  
Vol 412 (4-6) ◽  
pp. 395-398 ◽  
Author(s):  
Satoshi Sakamoto ◽  
Masanori Okumura ◽  
Zinggang Zhao ◽  
Yukio Furukawa

2015 ◽  
Vol 81 ◽  
pp. 83-89 ◽  
Author(s):  
Shufang Hu ◽  
Yanyan Feng ◽  
Daosen Zhang ◽  
Xiaoxu Lu ◽  
Jindong Tian ◽  
...  

2020 ◽  
Vol 22 (22) ◽  
pp. 12605-12612 ◽  
Author(s):  
Gaojie Zeng ◽  
Huanli Yuan ◽  
Juan Guo ◽  
Qiang Sun ◽  
Qilong Gao ◽  
...  

The thermal expansion curve of HfMgW3O12 correlated with hydration/dehydration accompanying structure and Raman spectral changes.


2000 ◽  
Vol 320 (3-4) ◽  
pp. 323-327 ◽  
Author(s):  
Hideyuki Nakayama ◽  
Ken-ichi Saitow ◽  
Maki Sakashita ◽  
Kikujiro Ishii ◽  
Keiko Nishikawa

2011 ◽  
Vol 31 (1) ◽  
pp. 53-57 ◽  
Author(s):  
Yusuke Imai ◽  
Takahiro Takekiyo ◽  
Hiroshi Abe ◽  
Yukihiro Yoshimura

2002 ◽  
Vol 56 (7) ◽  
pp. 909-915 ◽  
Author(s):  
Wei-Te Chen ◽  
Graham A. Bowmaker ◽  
John M. Seakins ◽  
Ralph P. Cooney

Far-infrared, mid-infrared, and Raman spectroscopy were used to characterize iodine-doped poly(isothianaphthene) (PITN) films and powders. The far-infrared and mid-infrared results show changes from absorption mode to reflective mode as the doping level increases, consistent with the iodine-doped PITN becoming more metallic and more conductive at higher doping levels. The far-IR and Raman (514.5-nm laser excitation) results show that I3− is dominant in iodine-doped PITN. The Raman spectral changes observed using 1064-nm excitation are different from those measured using 514.5-nm excitation. The spectra recorded with 514.5-nm excitation show features due to the undoped parts of the polymer, and these indicate that the effective conjugated chain length decreases with increased doping. The Raman spectra obtained by using 1064-nm excitation show features due to polaron and bipolaron states in the doped polymer.


1990 ◽  
Vol 5 (6) ◽  
pp. 1246-1252 ◽  
Author(s):  
J. C. Parker ◽  
R. W. Siegel

A Raman microprobe study of as-compacted nanophase TiO2 was carried out to investigate the spatial inhomogeneity of its anatase and rutile phases. Also, changes in the observed Raman spectra (line shifts and broadening) were investigated as a function of annealing at temperatures up to 600°C in argon or air. Microscopic phase inhomogeneity is observed and Raman spectral changes are shown to result from inhomogeneous oxygen deficiency in the nanophase TiO2. The line positions corresponding to the Raman active Eg modes in both anatase and rutile are found to be sensitive to this oxygen deficiency and are potential quantitative indicators of such deviations from stoichiometry.


1972 ◽  
Vol 26 (6) ◽  
pp. 579-584 ◽  
Author(s):  
A. L. Marston ◽  
S. F. Bush

Raman spectra of concentrated aqueous solutions of ferric chloride were recorded in the spectral range 50 to 500 cm−1. In near-saturated solutions, spectra show a four-line pattern typical of the tetrahedral FeCl4– complex: 390 cm−1 (w); 335 cm−1 (vs, p); 135 cm−1 (w); 110 cm−1 (s). At lower concentrations a new species dominates the spectrum, showing characteristic Raman lines at 318 cm−1 (s, p) and 165 cm−1 (vw). Conventional investigations of spectral changes with concentration of Fe(III) and chloride, coupled with group theoretical arguments, indicate that the stoichiometry of the complex must be FeCl3 or lower. Of the several symmetries that a FeCl3 complex might assume (C2v, C3v, D2h (dimer), and D3h), the D3h trigonal bipyramid structure FeCl3·2H2O with three equatorial chloride ligands and two axial waters is most compatible with the spectral evidence.


Sign in / Sign up

Export Citation Format

Share Document