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961.
Tangbin Zou Hongfu Wu Huawen Li Qing Jia Gang Song 《Journal of separation science》2013,36(20):3457-3462
Mangiferin is the main bioactive component in mango leaves, which possesses anti‐inflammatory, antioxidative, antidiabetic, immunomodulatory, and antitumor activities. In the present study, a microwave‐assisted extraction method was developed for the extraction of mangiferin from mango leaves. Some parameters such as ethanol concentration, liquid‐to‐solid ratio, microwave power, and extraction time were optimized by single‐factor experiments and response surface methodology. The optimal extraction conditions were 45% ethanol, liquid‐to‐solid ratio of 30:1 (mL/g), and extraction time of 123 s under microwave irradiation of 474 W. Under optimal conditions, the yield of mangiferin was 36.10 ± 0.72 mg/g, significantly higher than that of conventional extraction. The results obtained are beneficial for the full utilization of mango leaves and also indicate that microwave‐assisted extraction is a very useful method for extracting mangiferin from plant materials. 相似文献
962.
Saied Saeed Hosseiny Davarani Hamid Reza Moazami Ali Reza Keshtkar Mohammad Hossein Banitaba Saeed Nojavan 《Analytica chimica acta》2013
A novel method for the selective electromembrane extraction (EME) of U6+ prior to fluorometric determination has been proposed. The effect of extraction conditions including supported liquid membrane (SLM) composition, extraction time and extraction voltage were investigated. An SLM composition of 1% di-2-ethyl hexyl phosphonic acid in nitrophenyl octyl ether (NPOE) showed good selectivity, recovery and enrichment factor. The best performance was achieved at an extraction potential of 80 volts and an extraction time of 14 minutes Under the optimized conditions, a linear range from 1 to 1000 ng mL−1 and LOD of 0.1 ng mL−1 were obtained for the determination of U6+. The EME method showed good performance in sample cleanup and the reduction of the interfering effects of Mn2+, Zn2+, Cd2+, Ni2+, Fe3+, Co2+, Cu2+, Cl− and PO43− ions during fluorometric determination of uranium in real water samples. The recoveries above 54% and enrichment factors above 64.7 were obtained by the proposed method for real sample analysis. 相似文献
963.
964.
Min Lu Michael A. Phillips 《International journal of environmental analytical chemistry》2013,93(2):213-227
Antimony is an element of significant environmental concern, yet has been neglected relative to other heavy metals in electroanalysis. As such very little research has been reported on the electroanalytical determination of antimony at unmodified carbon electrodes. In this paper we report the electrochemical determination of Sb(III) in HCl solutions using unmodified carbon substrates, with focus on non-classical carbon materials namely edge plane pyrolytic graphite (EPPG), boron doped diamond (BDD) and screen-printed electrodes (SPE). Using differential pulse anodic stripping voltammetry, EPPG was found to give a considerably greater response towards antimony than other unmodified carbon electrodes, allowing highly linear ranges in nanomolar concentrations and a detection limit of 3.9?nM in 0.25?M HCl. Furthermore, the sensitivity of the response from EPPG was 100 times greater than for glassy carbon (GC). Unmodified GC gave a comparable response to previous results using the bare substrate, and BDD gave an improved, yet still very high limit of detection of 320?nM compared to previous analysis using an iridium oxide modified BDD electrode. SPEs gave a very poor response to antimony, even at high concentrations, observing no linearity from standard additions, as well as a major interference from the ink intrinsic to the working electrode carbon material. Owing to its superior performance relative to other carbon electrodes, the EPPG electrode was subjected to further analytical testing with antimony. The response of the electrode for a 40?nM concentration of Sb(III) was reproducible with a mean peak current of 1.07?µA and variation of 8.4% (n?=?8). The effect of metals copper, bismuth and arsenic were investigated at the electrode, as they are common interferences for stripping analysis of antimony. 相似文献
965.
Daura Vega Zoraida Sosa 《International journal of environmental analytical chemistry》2013,93(3):185-197
Abstract A sequential injection analysis method for the simultaneous spectrophotometric determination of phosphate and silicate has been developed. The method is based on the different reaction rates of the heteropolymolybdate formation reactions. Concentrations within the range 0.026—0.485 mmol P l?1 and 0.125—2.848 mmol Si l?1 have been determined at a frequency of 30 samples per hour. An R.S.D. of 2.1% was obtained for 0.162 mmol P l?1 and of 1.1% for 1.424 mmol Si l?1. The method was found to be suitable for the determination of phosphate and silicate in wastewater. 相似文献
966.
967.
Optimization of microwave‐assisted extraction for six inorganic and organic arsenic species in chicken tissues using response surface methodology 下载免费PDF全文
Response surface methodology was applied to optimize the parameters for microwave‐assisted extraction of six major inorganic and organic arsenic species (As(III), As(V), dimethyl arsenic acid, monomethyl arsenic acid, p‐arsanilic acid, and roxarsone) from chicken tissues, followed by detection using a high‐performance liquid chromatography with inductively coupled mass spectrometry detection method, which allows the simultaneous analysis of both inorganic and organic arsenic species in the extract in a single run. Effects of extraction medium, solution pH, liquid‐to‐solid ratio, and the temperature and time of microwave‐assisted extraction on the extraction of the targeted arsenic species were studied. The optimum microwave‐assisted extraction conditions were: 100 mg of chicken tissue, extracted by 5 mL of 22% v/v methanol, 90 mmol/L (NH4)2HPO4, and 0.07% v/v trifluoroacetic acid (with pH adjusted to 10.0 by ammonium hydroxide solution), ramping for 10 min to 71°C, and holding for 11 min. The method has good extraction performance for total arsenic in the spiked and nonspiked chicken tissues (104.0 ± 13.8% and 91.6 ± 7.8%, respectively), except for the ones with arsenic contents close to the quantitation limits. Limits of quantitation (S/N = 10) for As(III), As(V), dimethyl arsenic acid, monomethyl arsenic acid, p‐arsanilic acid, and roxarsone in chicken tissues using this method were 0.012, 0.058, 0.039, 0.061, 0.102, and 0.240 mg/kg (dry weight), respectively. 相似文献
968.
Preparation of novel ionic‐liquid‐modified magnetic nanoparticles by a microwave‐assisted method for sulfonylurea herbicides extraction 下载免费PDF全文
Ionic liquids immobilized on magnetic nanoparticles were prepared by an efficient microwave‐assisted synthesis method, and the properties of the ionic liquids were tuned based on the aromatic functional modification of its anion through a simple metathesis reaction. The novel as‐synthesized magnetic materials were characterized by various instrumental techniques. The magnetic nanoparticles have been utilized as adsorbents for the extraction of four sulfonylurea herbicides in tea samples, in combination with high‐performance liquid chromatography analysis. Significant extraction parameters, including type and volume of desorption solvent, extraction time, amount of adsorbent, and ionic strength were investigated. Under the optimum conditions, good linearity was obtained in the concentration range of 1–150 μg/L for metsulfuron‐methyl and bensulfuron‐methyl, and 3–150 μg/L for sulfometuron‐methyl and chlorimuron‐ethyl, with correlation coefficients R2 > 0.9987. Low limits of detection were obtained ranging from 0.13 to 0.81 μg/L. The relative standard deviations were 1.8–3.9%. Comparisons of extraction efficiency with conventional solid‐phase extraction equipped with a commercial C18 cartridge were performed. Results indicated that magnetic solid‐phase extraction is simple, time‐saving, efficient and inexpensive with the reusability of adsorbents. The proposed method has been successfully used to determine sulfonylurea herbicides from tea samples with satisfactory recoveries of 80.5–104.2%. 相似文献
969.
The use of microwave-assisted extraction has gained wide acceptance as a powerful tool for the recovery of environmental contaminants
and their subsequent analysis. This paper reviews the historical and fundamental basis of the technology. It also provides
a cursory review of the current state-of-the-art and literature (2000–2006) in the area of environmental analysis in addition
to providing a critical review of the level of efforts being devoted to its further development.
MAP is a Trademark of Her Majesty the Queen in Right of Canada as represented by the Minister of the Environment. 相似文献
970.
Robert Musiol Barbara Podeszwa Jacek Finster Halina Niedbala Jaroslaw Polanski 《Monatshefte für Chemie / Chemical Monthly》2006,137(9):1211-1217
Summary. Aromatic aldehydes undergo condensation with quinaldines under microwave irradiation to afford structurally diverse styrylquinolines
in high yields under solvent-free conditions. A comparison with the conventional method clearly indicates the advantages of
the new protocol. 相似文献