Spectrophotometric determination of total phenolics by solvent extraction and sorbent extraction optosensing using flow injection methodology

✍ Scribed by Wolfgang Frenzel; Stephanie Krekler

• Publisher: Elsevier Science
• Year: 1995
• Tongue: English
• Weight: 882 KB
• Volume: 310
• Category: Article
• ISSN: 0003-2670
• DOI: 10.1016/0003-2670(95)00141-l

✦ Synopsis

Flow injection ailalysis (FIA) procedures for the spectrophotometric determination of phenol involving m-line concentration by solvent and sorbent extraction have been developed. The imine product formed in the reaction between phenol and 4-aminoantipyrine (6AAP) is either extracted into chloroform (solvent extraction) or is temporarily retained on C,,-modified silica material contained in a microcolumn (sorbent extraction). In the latter case two variants of detection have been used namely the spectrophotometric measurement of the methanolic eluent containing the concentrated dye and at-column optosensing of the retained reaction product followed by methanol elution to maintain reversibility of the process. In the solvent extraction procedure a lo-fold increase of sensitivity compared to the common FIA method without extraction is achieved but no corresponding improvement in detectability is observed. Under optimized conditions the detection limit amounts to 8 pg 1-l. Using sorbent extraction methodology, high concentration factors can be obtained when large sample volumes are used. The only limitation in getting correspondingly lower detection limits are an increasingly high and variable blank value with sampling volume. The detection limits obtained for measurement of the absorbance in the eluent and on-column optosensing are 11 /*g 1-l and 0.4 pg l-', respectively. A study of the extractability of various phenol derivates using both solvent and sorbent extraction revealed lower relative response rates compared to the FL4 method without extraction. Phenolics that possess an additional acidic group are present in ionized form at the high pH of the assay and are not extractable at all.