Application Notebook
Low concentration natural methanol exists in most alcoholic beverages and usually causes no immediate health threat. Nevertheless, it is possible to have natural occurring methanol in beverages with concentration as high as 18 grams per liter of ethanol; or equivalent to 0.72% methanol in 40% ethanol, in alcohol (1). Current EU regulation limits naturally occurring methanol to below 10 grams per liter of ethanol; or equivalent to 0.4% methanol in 40% ethanol.
Low concentration natural methanol exists in most alcoholic beverages and usually causes no immediate health threat. Nevertheless, it is possible to have natural occurring methanol in beverages with concentration as high as 18 grams per liter of ethanol; or equivalent to 0.72% methanol in 40% ethanol, in alcohol (1). Current EU regulation limits naturally occurring methanol to below 10 grams per liter of ethanol; or equivalent to 0.4% methanol in 40% ethanol.
Raman spectroscopy has been shown to be an effective tool in compositions analysis as well as adulteration identifications in foods (2). In the alcoholic beverage industry, the standard composition analysis method were more expensive and time-consuming gas chromatography (3). Here, we present a Raman spectroscopy method for a quick and lower cost alternative to verify the existence of low concentration methanol in alcohol.
40% ethanol/water solution was prepared using 200-proof ethanol and distilled water. HPLC grade methanol was added into the 40% ethanol solution to make samples with methanol concentration ranging from 50 ppm to 2.5%. An Enwave Optronics' ProRaman instrument with laser excitation at 785 nm was used for the measurements. The sample solutions were measured in quartz cuvette in a sample holder. Figure 1 depicts the results of the measured spectra in the fingerprint region of the Raman spectra.
Figure 1: The fingerprint range spectra of the various solutions.
Partial least square (PLS) regression method was used for calibration and prediction model for methanol. The spectral region from 950–1200 cm-1 was chosen for developing the calibration model. The actual vs. predicted concentration value of methanol is shown in Figure 2. It is shown that the measured data and PLS prediction match very well with correlation coefficient R2 @ 0.997.
Figure 2: Actual and predicted methanol concentrations using PLS regression model.
An affordable, high sensitivity ProRaman instrument was used with PLS method to successfully analyze low concentration methanol in 40% alcohol. Based on our findings, the detection limit for methanol in 40% of ethanol is much better than 50 ppm and reliable quantitative determination using PLS prediction could reach 50 ppm of methanol in 40% alcohol.
(1) F. Bindler, E. Voges, and P. Laugel, "The Problem of Methanol Concentration Admissible in Distilled Fruit Spirits," Food Addit. Contam. 5, 343–351 (1988).
(2) W.M. Mackenzie and R.I. Aylott, "Analytical Strategies to Confirm Scotch Whisky Authenticity," The Analyst 129, 607–612 (2004).
(3) L.M. Reid, C.P. O'Donnell, and G. Downey, "Recent Technological Advances for the Determination of Food Authenticity," Trends in Food Science & Technology 17, 344–353 (2006).
Enwave Optronics, Inc.
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Website: www.enwaveopt.com
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