scholarly journals Formaldehyde Analysis in Non-Aqueous Methanol Solutions by Infrared Spectroscopy and Electrospray Ionization

2021 ◽  
Vol 9 ◽  
Author(s):  
Krishna K. Barakoti ◽  
Pradeep Subedi ◽  
Farzaneh Chalyavi ◽  
Salvador Gutierrez-Portocarrero ◽  
Matthew J. Tucker ◽  
...  

We present the analysis of formaldehyde (HCHO) in anhydrous methanol (CH3OH) as a case study to quantify HCHO in non-aqueous samples. At higher concentrations (C > 0.07 M), we detect a product of HCHO, methoxy methanol (MM, CH3OCH2OH), by Fourier transform infrared spectroscopy, FTIR. Formaldehyde reacts with CH3OH, CD3OH, and CD3OD as shown by FTIR with a characteristic spectral feature around 1,195 cm−1 for CH3OH used for the qualitative detection of MM, a formaldehyde derivative in neat methanol. Ab initio calculations support this assignment. The extinction coefficient for 1,195 cm−1 is in the order of 1.4 × 102 M−1cm−1, which makes the detection limit by FTIR in the order of 0.07 M. For lower concentrations, we performed the quantitative analysis of non-aqueous samples by derivatization with dinitrophenylhydrazine (DNPH). The derivatization uses an aqueous H2SO4 solution to yield the formaldehyde derivatized hydrazone. Ba(OH)2 removes sulfate ions from the derivatized samples and a final extraction with isobutyl acetate to yield a 1:1 methanol: isobutyl acetate solvent for injection for electrospray ionization (ESI). The ESI analysis gave a linear calibration curve for concentrations from 10 to 200 µM with a time-of-flight analyzer (TOF). The detection and quantification limits are 7.8 and 26 μM, respectively, for a linear correlation with R2 > 0.99. We propose that the formaldehyde in CH3OH is in equilibrium with the MM species, without evidence of HCHO in solution. In the presence of water, the peaks for MM become less resolved, as expected from the well-known equilibria of HCHO that favors the formation of methylene glycol and polymeric species. Our results show that HCHO, in methanol does not exist in the aldehyde form as the main chemical species. Still, HCHO is in equilibrium between the production of MM and the formation of hydrated species in the presence of water. We demonstrate the ESI-MS analysis of HCHO from a non-aqueous TiO2 suspension in methanol. Detection of HCHO after illumination of the colloid indicates that methanol photooxidation yields formaldehyde in equilibrium with the solvent.

2002 ◽  
Author(s):  
Rohit Srivastava ◽  
Gururaj U. Shenoy ◽  
Scott Forrest ◽  
S. Chinnayelka ◽  
Ronald S. Besser ◽  
...  

2007 ◽  
Vol 15 (2) ◽  
pp. 115-121 ◽  
Author(s):  
B. Jagannadha Reddy ◽  
Ray L. Frost

In this endeavour, near infrared spectroscopy studies show evidence of variable composition in aurichalcite minerals of zinc copper carbonate hydroxides. The observation of a broad feature in the electronic part of the spectrum around 11,500 cm−1 (870 nm) is a strong indication of Cu2+ substitution for Zn2+ in the mineral. Overtones of OH vibrations in the spectra from 7250 to 5400 cm−1 (1380–1850 nm) show strong hydrogen bonding in these carbonates. A band common to spectra of all carbonates appears near 5400 cm−1 (1850 nm) due to the combination of both OH-stretching and HOH-bending vibrations, which may be attributed to adsorbed water. Aurichalcite minerals display a spectral sequence of five absorption bands with variation of both band positions and intensities and this is the chief spectral feature observed in the range 5200–5100 cm−1 (1920–2380 nm) due to vibrational processes of the carbonate ion. The frequency shift of carbonate bands suggests the effect of divalent cations and/or variations of the Zn/Cu ratio in aurichalcite minerals.


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