FIRST FAR-IR SPECTRA OF 2,2-D2-PROPANE: THE ν9 (A1) B-TYPE BAND NEAR 365.3508 cm−1. THE DETERMINATION OF GROUND AND UPPER STATE CONSTANTS.

Author(s):  
Daniel Gjuraj ◽  
Brant Billinghurst ◽  
Jean-Marie Flaud ◽  
Walter Lafferty ◽  
Robert Grzywacz ◽  
...  
Keyword(s):  
2021 ◽  
Vol 34 (7) ◽  
pp. 483-487
Author(s):  
L.N. Sinitsa ◽  
N.M. Emel’yanov ◽  
A.A. Lugovskoi ◽  
A.P. Shcherbakov ◽  
V.V. Annenkov

2002 ◽  
Vol 56 (10) ◽  
pp. 1259-1267 ◽  
Author(s):  
Cyril Petibois ◽  
Georges Cazorla ◽  
André Cassaigne ◽  
Gérard Déléris

Global metabolic adaptations to physical conditioning were described in 15 subjects by FT-IR spectrometry as the method allowed determination of glucose (Glc), lactate (La), glycerol, triglycerides (TG), fatty acyl moieties (FAM), and total amino acids plasma concentrations. Subtraction of plasma FT-IR spectra obtained at resting state from the exercise spectra also allowed determination of the biomolecular response to exercise. On week 1, exercise induced a transient hypoglycemia, a lactatemia increase of 153%, a FAM depletion of 27%, and a TG concentration decrease of 28%. Protein contents increased by 2%, but these were partly catabolized for amino acid supply (+27%), suggesting an important metabolic stress during exercise. On week 3, exercise hypoglycemia had disappeared, lactate increase was diminished by 91%, TG contents were decreased by 14%, and proteins and amino acids exhibited higher absorption increases. On week 5, TG and FAM concentrations were markedly increased during exercise, protein absorption was still increased (+9%), but amino acid blood release was diminished by 81%. These results described positive adaptations to training. Furthermore, FAM concentration could be determined from plasma FT-IR spectra by using the 2996–2819 cm−1 spectral area [ νas(CH3), νas(CH2), νs(CH3), and νs(CH2) absorbance; 0.82 mMol·L−1, a.u. cm−1], as well as for amino acid concentration by using the ν(COO−) spectral area (1430–1360 cm−1; 0.062 g·L−1, a.u. × cm−1). FT-IR spectrometry was useful to determine simultaneously various plasma concentrations and most of the biomolecular changes through successive samples.


2012 ◽  
Vol 260-261 ◽  
pp. 593-597
Author(s):  
Veronika Sassmanová ◽  
Zuzana Poláčková ◽  
Jaroslav Frantík ◽  
Stanislav Honus ◽  
Dagmar Juchelková

The article deals with the identification of a chemical structure of pyrolysis liquid occurring by the thermal degradation of tyre debris within the temperature interval from 500°C to 650°C and the temperature increase steps of 50°C in individual experiments and with the use of analytical methods GC/MS, FT-IR and the elementary analysis. The measured FT-IR spectra indicate the representation of functional groups included in measured samples. They could be used for the determination of basic chemical properties. There were changes in the chemical composition monitored as well as the creation of functional groups in the pyrolysis liquid on the basis of FT-IR spectra and GS/MS outcomes.


2014 ◽  
Vol 13 (3) ◽  
pp. 169-170
Author(s):  
Moe SAKURAI ◽  
Hiroshi SAKUMA ◽  
Noriyoshi TSUJINO ◽  
Eiichi TAKAHASHI ◽  
Katsuyuki KAWAMURA
Keyword(s):  

1973 ◽  
Vol 28 (3-4) ◽  
pp. 153-157 ◽  
Author(s):  
R. N. Prasad ◽  
J. P. Tandon

Reactions of aluminium iso-propoxide with monofunctional bidentate Schiff bases having the general formula 2-HOC10H6CH:NR (where R = C2H5, n C3H7, iso-C3H7, n-C4H9, iso-C4H9, sec-C4H9, tert-C4H9 and C6H5) in different stoichiometric ratios have yielded Al(OPri)2(SB), Al(OPri)(SB)2 and Al(SB)3 type of products (where SB is the anion of the corresponding Schiff base, SBH). The ebullioscopic determination of molecular weights shows that the di-iso-propoxy mono- Schiff base derivatives are dimeric; the tris- Schiff base derivatives are monomeric and for the mono-iso-propoxy bis- Schiff base derivatives, molecular association is ~1.4. The IR spectra of a few representative derivatives have been recorded and possible structures indicated.


Sign in / Sign up

Export Citation Format

Share Document