Search

A method for simultaneous determination of acetaldehyde, propionaldehyde, acrolein, and crotonaldehyde in gas phase of cigarette mainstream smoke by headspace gas chromatography-mass spectrometry was developed and validated. Gas phase components of mainstream cigarette smoke were extracted with methanol, and then the samples were separated on a DB 624 (60 m, 0.32 mm x 1.8 mm) column, analyzed with headspace gas chromatography-mass spectrometry, and quantified by isotope internal standard. The linearities of acetaldehyde, propionaldehyde, acrolein, and crotonaldehyde were good (R2>0.992). The recoveries of acetaldehyde, propionaldehyde, acrolein, and crotonaldehyde were between 78.5% and 115%. The relative standard deviations were less than 10%. The limits of detection and limits of quantitation were 0.014 μg/cigarette ~0.12 μg/cigarette and 0.045 μg/cigarette ~0.38 μg/cigarette, respectively. The method had advantage of high sensitivity, it did not require derivatization of 2,4-dinitrophenylhydrazine and avoided a large number of adverse reactions during the process of derivation to improve the accuracy of result, and it was suitable for quantitative analysis of four aldehydes in gas phase of cigarette mainstream smoke. [ABSTRACT FROM AUTHOR]

This paper presents low-cost and recyclable activated carbon (XLAC) derived from Xanthoceras sorbifolia Bunge hull for high-efficiency adsorption of Cd(II) and Hg(II) ions in industrial wastewater. XLAC was prepared through H3PO4 activation and was characterized using N2 adsorption-desorption, scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDX), and Fourier transform infrared (FTIR) spectroscopy. In single-metal-system adsorption experiments, the maximum adsorption capacities for Cd(II) and Hg(II) obtained under different experimental conditions were 388.7 and 235.6 mg·g−1, respectively. All adsorption equilibrium data fit perfectly with the Langmuir isotherm model. In a binary metal system, competitive studies demonstrated that the presence of Cd(II) significantly decreased the adsorption of Hg(II), but the adsorption of Cd(II) showed a little change in the presence of Hg(II). In addition, XLAC can be regenerated with a 0.01 mol·L−1 HNO3 solution and reused at least four times. The FTIR spectra revealed that a chemical interaction occurs between functional groups containing lone electron pairs in XLAC and metal ions. Overall, these results suggest that XLAC may be suitable as an adsorbent for heavy metal removal from wastewater streams. [ABSTRACT FROM AUTHOR]

A liquid chromatographic tandem mass spectrometry method (LC-MS/MS) for the simultaneous determination of 1-hydroxypyrene (1-OHP), 3-hydroxybenzo[a]pyrene (3-OHBaP), and 3-hydroxybenz[a]anthracene (3-OHBaA) in human urine has been developed. With the exception of 3-OHBaP at a low spiking level, the average recoveries were greater than 80%. The method has good accuracy (72.1–107.7%) and reproducibility (1.8–11.4%) and was successfully used to study the uptake of pyrene, benzo[a]pyrene, and benzo[a]anthracene from cigarette smoke. The results indicated that urinary 1-OHP concentration in the smoking group (66.58 ± 70.91 ng/g creatinine) was higher than that observed in the nonsmoking group (58.16 ± 49.48 ng/g creatinine). Urinary 3-OHBaA concentrations in nonsmokers and smokers with 8 mg and 10 mg tar cigarettes were 10.98 ± 4.39 ng/g creatinine, 11.01 ± 13.30 ng/g creatinine, and 9.17 ± 12.89 ng/g creatinine, respectively. Urinary 3-OHBaP concentrations in nonsmokers and smokers with 8 mg and 13 mg tar cigarettes were 1.30 ± 0.20 ng/g creatinine, 2.83 ± 1.78 ng/g creatinine, and 6.00 ± 4.44 ng/g creatinine, respectively. Urinary 1-OHP levels exhibited a significant correlation with BaP yield in cigarette smoke under the Canadian intense smoking condition (y=3.5563x+30.171, R2=0.9916, n=227). [ABSTRACT FROM AUTHOR]

The decay resistance of wood can be improved via a vacuum heat treatment. The amount of nutrients from cellulose, hemicellulose, and lignin and amount of sugars needed by the fungi during their growth were investigated. The results showed that the absorbance peaks corresponding to absorbed CH3-CH2-, C=O, and the benzene ring skeleton stretching vibration all noticeably weakened with increased heat treatment. This indicated that the cellulose, hemicellulose, and lignin degraded to varying degrees. The specimens with a higher initial moisture content (MC) showed greater amounts of nutrient degradation after 2 h at the same heat treatment temperature. The chemical analysis results were in good agreement with the Fourier transform infrared (FTIR) analysis results. The decay resistance tests showed that the average mass loss of the heat-treated specimens was up to 10.8%, in contrast to 22.23% for the untreated specimens. Furthermore, the FTIR analysis of the heat and decay-resistance test showed that the vibration wave peaks that corresponded to CH3-CH2- at 2954 cm−1 showed noticeably less separation at higher heating temperature. This demonstrated that the cellulose hydrolysis in the wood decreased at higher heating temperatures, which explained why the decay resistance increased with increased heat treatment. [ABSTRACT FROM AUTHOR]