Abstract

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 R 2 > 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.

Highlights

  • We present the analysis of formaldehyde in anhydrous methanol

  • In the Supplementary Material (SM), we present the single beam spectra for the CH3OH and the MM spectra obtained by bubbling HCHO into CH3OH

  • To quantify HCHO in CH3OH, we demonstrated the derivatization with DNPH in an aqueous H2SO4 solution

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Summary

Introduction

We present the analysis of formaldehyde in anhydrous methanol. Our motivation for this analysis stems from the need of quantifying the product of methanol photooxidation. Our results will show that formaldehyde is not the predominant species in MeOH because it reacts with the solvent to produce the hemiacetal methoxymethanol (MM) We propose this is a competitive equilibrium in the absence of water. The molecule has been classified as a carcinogen by the United States National Toxicology Program (NTP National Toxicology Program, 2016) and formaldehyde preservatives found in cosmetics, medications, and household products require investigation (Benassi et al, 1991; Boyer et al, 2013) It is used as an antiseptic and one of the main ways to preserve tissues in the lab (Dubos, 1938; Maeda et al, 2014)

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