scholarly journals Short-wavelength optoacoustic spectroscopy based on water muting

2020 ◽  
Vol 117 (8) ◽  
pp. 4007-4014 ◽  
Author(s):  
Jaya Prakash ◽  
Mir Mehdi Seyedebrahimi ◽  
Ara Ghazaryan ◽  
Jaber Malekzadeh-Najafabadi ◽  
Vipul Gujrati ◽  
...  

Infrared (IR) optoacoustic spectroscopy can separate a multitude of molecules based on their absorption spectra. However, the technique is limited when measuring target molecules in aqueous solution by strong water absorption at IR wavelengths, which reduces detection sensitivity. Based on the dependence of optoacoustic signal on the temperature of the probed medium, we introduce cooled IR optoacoustic spectroscopy (CIROAS) to mute water contributions in optoacoustic spectroscopy. We showcase that spectral measurements of proteins, lipids, and glucose in the short-wavelength IR region, performed at 4 °C, lead to marked sensitivity improvements over conventional optoacoustic or IR spectroscopy. We elaborate on the dependence of optoacoustic signals on water temperature and demonstrate polarity changes in the recorded signal at temperatures below 4 °C. We further elucidate the dependence of the optoacoustic signal and the muting temperature on sample concentration and demonstrate that changes in these dependences enable quantification of the solute concentration. We discuss how CIROAS may enhance abilities for molecular sensing in the IR.

1979 ◽  
Vol 32 (8) ◽  
pp. 1661 ◽  
Author(s):  
T Woon ◽  
MJ O'Conner

The quadridentate ligand, (2S,2'S)-1,1'-(ethane-1,2-diyl)bis(pyrrolidine-2-carboxylic acid) dihydrochloride (H2pren,2HCl), has been derived from (S)-proline. The preparations of the cobalt(III) complexes Na [Co(pren)(CO3)],3H2O, [CO(pren)(H2O)2] ClO4,- 2H2O and [Co(pren)(H2O)Cl],1�5H2O are described. All exist as cis-α geometrical isomers. 13C N.M.R. and absorption spectral measurements confirm the cis-α arrangement. The complex cis-α- [Co(pren)(H2O)Cl],1�5H2O rapidly aquates with retention of configuration. The compounds having actual or near C2 symmetry exhibit a strong negative c.d. band under the 1A1g → 1T1g cubic absorption band which is due to the 1A1 →1E tetragonal component, consistent with the Δ absolute configuration imposed by the (S) configuration of the asymmetric carbon atom in the (S)-proline moiety. The o.r.d. spectrum of cis-α-Na [Co(pren)CO3],3H2O in aqueous solution has a negative Cotton effect at low energy as expected for the Δ absolute configuration.


Clay Minerals ◽  
1983 ◽  
Vol 18 (3) ◽  
pp. 253-265 ◽  
Author(s):  
P. J. Isaacson ◽  
B. L. Sawhney

AbstractThe sorption and transformation of phenol, 2-methylphenol, 3-methylphenol, 2,6-dimethylphenol, 3,5-dimethylphenol, and 2,4,6-trimethylphenol, by homoionic Na-, H-, Ca-, Cu-, Al-, and Fe(III)-montmorillonite from both vapour and aqueous phases were examined by IR spectroscopy. All the phenols were sorbed by the clays but were modified to different degrees depending on the exchangeable cations and on the amount and type of alkyl substitution of the phenols. Sorption of 2,6-dimethylphenol from aqueous solution was irreversible, and the extent of sorption followed the order Fe- > Al- > Cu- > Ca-clay. Both transition and non-transition metal cations were effective in transforming the phenol sorbates and heating the clay/phenol complexes further enhanced transformation. The results are discussed in terms of the nature of the transformation products and the likely role of radical reactions in their formation.


1984 ◽  
Vol 114 ◽  
pp. 455-458 ◽  
Author(s):  
Anders Eriksson ◽  
Olof Kristiansson ◽  
Jan Lindgren

2007 ◽  
Vol 60 (1) ◽  
pp. 68 ◽  
Author(s):  
Brendan F. Abrahams ◽  
Nicholas J. FitzGerald ◽  
Timothy A. Hudson ◽  
Richard Robson ◽  
Richard D. Shalders

A hydrogen bonded network of composition Zn8(C4O7)4(H2O)12·hydrate was shown to undergo a single crystal to single crystal exchange process when crystals are immersed in a concentrated aqueous solution of Ni(ii). In the exchange process, half of the zinc(ii) centres are replaced by nickel(ii) centres. The process of metal ion exchange was monitored using IR spectroscopy. Crystal structures of the transformed crystal and the product generated from a direct synthetic approach are presented.


From competition studies on γ -irradiated solutions containing Ir(III), Ir(IV) or Pt(II) and N 2 O, G e - aq+ was found to be 3.10 ± 0.10 at natural pH. In confirmation of previous measurements the electron yield increased in alkaline solution. Measurements of molecular yields in the iridium system indicate that at zero solute concentration at natural pH, G 0 H 2 = 0.44 ± 0.02 and G 0 H 2 O 2 = 0.78 ± 0.05. In alkaline solutions both Pt(IV) and Ir(III) are thermally and photochemically labile. From competition studies at natural pH k ( e - + Ir(III)) = 7.4 x 10 9 M -1 s -1 and k ( e - + Ir(IV)) = 2.6 x 10 10 M -1 s -1 and at pH 13 k ( e - + Ir(III)) = 1.0 x 10 10 M -1 s -1 and from pulsing experiments k ( e - + Pt(II)) = 6.7 x 10 9 M -1 s -1 and k ( e - + Pt(IV)) = 3.6 x 10 10 M -1 s -1 .


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