US EPA

326167 

Journal Article 

UV-vis spectrophotometric method for the quantitation of all the components of italian general denaturant and its application to check the conformity of alcohol samples 

Bucci, R; Balestrieri, F; Magri, AD; Magi, AL; Marini, F 

2006 

1 

Talanta
ISSN: 0039-9140
EISSN: 1873-3573 

68 

3 

781-790 

English 

18970391 

10.1016/j.talanta.2005.06.002 

WOS:000234955400044 

A simple, fast and relatively inexpensive spectrophotometric method for the identification and the quantification of the individual components of the Italian general denaturant in alcohol samples is proposed. In particular, it is shown that bitrex (a quaternary ammonium salt), whose UV spectrum is completely masked by those of the other denaturant components, can be identified using its reaction with disulphine blue VN-150 (an anionic dye indicator), which leads to the formation of an intensely colored ion-association complex (mole ratio 1:1), easily extractable in chloroform. As far as the quantitative detection is involved, it is however necessary to shake the chloroform phase in the presence of 1 mol L[sub]-1[/sub] NaClO[sup]4[/sup] aqueous solution because of the fast adsorption of the ion pair on the walls of the glass cell. Perchlorate anion, due to mass action, substitutes the anionic dye indicator in the association complex: as a consequence, disulphine blue passes to the aqueous phase, where its absorbance at λ = 640 nm is measured. On the other hand, C.I. Reactive Red 24 dye is easily identifiable from the visible spectrum of the product without any further pretreatment: its concentration can be determined measuring the absorbance at >. = 542 nm. Thiophene, being significantly more concentrated than the other components, can be identified from the UV spectrum of a 1:100 diluted solution of the alcohol sample and quantitatively determined measuring the absorbance at λ=230nm. Lastly, methyl ethyl ketone (MEK) can be identified from the UV spectrum of a 1:5 diluted solution of the alcohol sample and quantitatively determined measuring the absorbance at λ = 273 nm. However, more accurate results can be obtained using a multiwavelength analysis in the range 220-250 and 250-310nm for the determination of thiophene and MEK, respectively. Validation on standard denatured alcohol samples has proven the method to be both accurate and sufficiently precise (within- and between-days repeatability <5%) to be applied to the analysis of real commercial samples. (English) 

Denatured alcohol; Spectrophotometry; General denaturant components; Perchlorate; Verre; Chloroforme; Plomb; Colorant réactif; Ammonium; Alcool; Enrichissement chimique; Répétabilité; Cétone; Thiophène; Prétraitement; Spectrométrie absorption; Paire ion; Adsorption; Solution aqueuse; Association ionique; Analyse quantitative; Spectrophotométrie; Spectrométrie UV visible; Perchlorates; Glass; Chloroform; Lead; Reactive dye; Alcohol; Chemical enrichment; Repeatability; Ketone; Thiophene; Pretreatment; Absorption spectrometry; Ion pair; Aqueous solution; Ionic association; Quantitative analysis; Ultraviolet visible spectrometry; Perclorato; Vidrio; Plomo; Colorante reactivo; Amonio; Enriquecimiento químico; Repetibilidad; Cetona; Tiofeno; Pretratamiento; Espectrometría absorción; Par ión; Adsorción; Solución acuosa; Asociación iónica; Análisis cuantitativo; Espectrofotometría; Espectrometría UV visible