YuHua Shi

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Name: 师宇华; Shi, YuHua
Organization: Jilin University , China
Department:
Title: Associate Professor(PhD)

TOPICS

Co-reporter:Hongmin Wei;Jinjuan Yang;Hanqi Zhang
Journal of Separation Science 2014 Volume 37( Issue 17) pp:2349-2356
Publication Date(Web):
DOI:10.1002/jssc.201400313

A simple, rapid, and efficient method of ultrasonic nebulization extraction assisted dispersive liquid–liquid microextraction was developed for the simultaneous determination of six parabens in cosmetic products. The analysis was carried out by gas chromatography. Water was used as the dispersive solvent instead of traditional organic disperser. The experimental factors affecting the extraction yield, such as the extraction solvent and volume, extraction time, dispersive solvent and volume, ionic strength, and centrifuging condition were studied and optimized in detail. The limit of detections for the target analytes were in the range of 2.0–9.5 μg/g. Good linear ranges were obtained with the coefficients ranging from 0.9934 to 0.9969. The proposed method was successfully applied to the analysis of six parabens in 16 cosmetic products. The recoveries of the target analytes in real samples ranged from 81.9 to 108.7%, and the relative standard deviations were <5.3%.

Co-reporter:Jinjuan Yang;Hongmin Wei;Xiane Teng;Hanqi Zhang
Phytochemical Analysis 2014 Volume 25( Issue 2) pp:178-184
Publication Date(Web):
DOI:10.1002/pca.2490

ABSTRACT

Introduction

Ionic liquids have attracted much attention as an extraction solvent instead of traditional organic solvent in single-drop microextraction. However, non-volatile ionic liquids are difficult to couple with gas chromatography. Thus, the following injection system for the determination of organic compounds is described.

Objective

To establish an environmentally friendly, simple, and effective extraction method for preparation and analysis of the essential oil from aromatic plants.

Methods

The dynamic ultrasonic nebulisation extraction was coupled with headspace ionic liquid-based single-drop microextraction(UNE–HS/IL/SDME)for the extraction of essential oils from Forsythia suspense fruits. After 13 min of extraction for 50 mg sample, the extracts in ionic liquid were evaporated rapidly in the gas chromatography injector through a thermal desorption unit (5 s). The traditional extraction method was carried out for comparative study.

Results

The optimum conditions were: 3 μL of 1-methyl-3-octylimidazolium hexafluorophosphate was selected as the extraction solvent, the sample amount was 50 mg, the flow rate of purging gas was 200 mL/min, the extraction time was 13 min, the injection volume was 2 μL, and the thermal desorption temperature and time were 240 °C and 5 s respectively. Comparing with hydrodistillation (HD), the proposed method was environment friendly and efficient.

Conclusion

The proposed method is environmentally friendly, time saving, with high efficiency and low consumption. It would extend the application range of the HS/SDME and would be useful especially for aromatic plants analysis. Copyright © 2013 John Wiley & Sons, Ltd.

Co-reporter:Hongmin Wei;Jinjuan Yang;Hanqi Zhang
Chemical Research in Chinese Universities 2014 Volume 30( Issue 3) pp:368-373
Publication Date(Web):2014 June
DOI:10.1007/s40242-014-3566-4
A simple and rapid sample preparation method of dispersive liquid-liquid microextraction(DLLME) was applied in the simultaneous determination of six parabens in the aqueous cosmetics. The analysis was performed on gas chromatography coupled with a flame ionization detection(GC-FID). The mixed solution containing 30 μL of chloroform(extraction solvent) and 300 μL of tetrahydrofuran(dispersive solvent) was rapidly injected into the sample solution for the purpose of microextraction. After that, the solution mentioned above was centrifuged at 4000 r/min for 10 min, and then the organic sediment phase was detected by GC-FID. The effects of experimental parameters, such as the extraction solvent and the volume of it, and the dispersive solvent and the volume of it, on the yield of the extraction were studied in detail. Under the optimum conditions, the enrichment factors of the target analytes range from 87 to 214. Linearity ranges are 0.05–10.0 μg/mL for methylparaben and 0.025–5.0 μg/mL for the other five parabens. The relative standard deviations(RSDs) are lower than 8.2%(n=6). The proposed method was applied to the analysis of six parabens in eleven aqueous cosmetics. The recoveries of the target analytes in the spiked real samples are in the range of 81.0%–103%.
Co-reporter:Cui Yu;Jinjuan Yang;Yeqiang Wang;Hongmin Wei;Hanqi Zhang
Phytochemical Analysis 2013 Volume 24( Issue 4) pp:296-302
Publication Date(Web):
DOI:10.1002/pca.2410

ABSTRACT

Introduction

As the concentrations of the volatile organic compounds are always low and their matrix is complex, it is necessary to pre-concentrate the volatile organic compounds before analysis. Ultrasonic nebulisation extraction with a self-made extraction column coupled with liquid phase microextraction is developed for the extraction of active constituents from spices.

Objective

To develop an environmentally compatible extraction technique for the preparation and analysis of the volatile organic compounds from spices.

Method

The sample is placed into the nebulisation vessel of a nebulisation humidifier and a purging gas is blown through the vessel continuously. When the nebuliser is switched on, a ultrasonic fountain is formed by ultrasonic vibration and the target analytes are transferred from the sample solution to the vapour phase and then concentrated on the extraction solvent in the extraction column. After extraction for 3 min and allowed to stand upright for 5 min, the extract is analysed by GC and GC–MS. Different methods of comparison can then be carried out.

Results

Optimum conditions were found to be: 30 μL of n-tetradecane as the extraction solvent, a flow rate for the purging gas of 40 mL/min, a purging time of 3 min and a standing time was 5 min. The contents of constituents in the extract obtained by the proposed method were close to those obtained by hydrodistillation (HD). Moreover, the proposed method achieves higher enrichment efficiency.

Conclusion

A method was developed for the extraction of volatile organic compounds from spices. The study has shown that it is a fast and environmentally sustainable technique. Copyright © 2012 John Wiley & Sons, Ltd.

Co-reporter:Jinjuan Yang;Hongmin Wei;Cui Yu;Hanqi Zhang
Chromatographia 2012 Volume 75( Issue 23-24) pp:1435-1443
Publication Date(Web):2012 December
DOI:10.1007/s10337-012-2335-0
Hydrodistillation (HD) coupled with headspace single-drop microextraction by using ionic liquid (IL) as the extraction solvent, followed by gas chromatography analysis technique, was successfully developed to determine the volatile and semivolatile compounds in seeds of Cuminum cyminum L. In the proposed method, a 1.5-μL microdrop of 1-octyl-3-methylimidazolium hexafluorophosphate, working as the extraction solvent was suspended in the headspace of a 50-mL round-bottom sample flask. After extracting for 30 min, both IL and target analytes were injected into the gas chromatographic system by thermal desorption for 5 s under 240 °C. Then, the IL was retracted back to the microsyringe. Thus, the capillary column should not be contaminated and a clean chromatogram was obtained. The parameters affecting extraction performance were investigated and optimized. The extraction efficiency of the proposed method was compared with that of HD, which is a standard extraction method. The contents of constituents in the extract obtained by the proposed method were close to those obtained by HD. It seems to be an environmentally friendly, time-saving, high efficiency and low solvent consumption technique and would be useful, especially for aromatic plants analysis.
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