## Abstract A validated gas chromatographic method for the determination of triclosan in human dental plaque is described. Based on plaque sample weights of 10 mg, the limit of detection (2 Γ __S/N__) is 0.5 ΞΌg/g. The method is linear (__r__ = 0.9986) from the limit of detection to 50 ΞΌg/g. Recover
Determination of the volatiles from tobacco by capillary gas chromatography with atomic emission detection and mass spectrometry
β Scribed by Gang Li; Da Wu; Ye Wang; Wenyan Xie; Xiangmin Zhang; Baizhan Liu
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 195 KB
- Volume
- 35
- Category
- Article
- ISSN
- 1615-9306
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β¦ Synopsis
Abstract
A new gas chromatographβatomic emission detector (GCβAED) coupled with Deans switching technique for analyzing volatiles from tobaccos were developed. The detector operating parameters (reagent gas pressure and makeβup gas flow rate) were optimized. The detection limits for the elements carbon (193βnm), hydrogen (486βnm) and oxygen (171βnm) ranged 0.05β0.2, 0.05β0.3 and 1β11βng, respectively, depending on the compound. The sensitivity and linearity for the elements carbon (193βnm), hydrogen (486βnm) and oxygen (171βnm) decreased in the order O>H>C. Calibration curves were obtained by plotting peak area versus concentration, and the correlation coefficients relating to linearity were at least 0.9359. Elemental response factors measured on these channels, relative to the carbon 193βnm channel, were hydrogen, 0.38β0.48 (mean %RSD=5.64), and oxygen, 0.085β0.128 (mean %RSD=14.9). The evaluation was also done for the new technique and for an established GCβMS technique for the same real samples. The results of GCβAED and GCβMS showed that there was a relatively good agreement between the two sets of data.
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