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91.
《Analytical letters》2012,45(11):1620-1631
Abstract A rapid, simple, and efficient liquid-phase microextraction (LPME) method coupled with high-performance liquid chromatography and ultraviolet detection for the analysis of triazine herbicides was developed in this study. Under the optimum conditions, the enrichment factors and extraction recoveries were 33.0–72.6 and 11.2–23.2%, respectively. The detection limits (LODs) were in the range of 0.03–0.10 µg L?1. The relative standard deviations for the determination of the triazine herbicides at μg L?1 levels varied in the range 2.05–8.15%. The method was successfully applied in the determination of the triazine herbicides in aqueous samples with satisfactory results. 相似文献
92.
《Analytical letters》2012,45(6):1012-1024
A highly sensitive method for the determination of the chloroacetanilide herbicides alachlor, acetochlor, pretilachlor, butachlor, and metolachlor in environmental water samples was developed. It is based on solid-phase extraction using magnetic graphene nanocomposite (G-Fe3O4) as the adsorbent, followed by gas chromatography with electron capture detection. This novel adsorbent showed a great adsorptive ability toward the analytes. The main experimental parameters such as the amount of G-Fe3O4, extraction time, ionic strength, the pH of the sample solution, and desorption conditions were optimized. Under the optimum conditions, the enrichment factors of the method for the analytes were in the range from 649 to 1078. A good linear response was achieved in the range of 0.2–20.0 ng mL?1, with correlation coefficients (r) varying from 0.9964 to 0.9998. The limits of detection of the method ranged from 0.02 to 0.05 ng mL?1 and the relative standard deviations were below 4.5%. The method was successfully applied to the determination of the herbicides in environmental water samples. Recoveries of the method for the analytes were in the range of 80.7–105.3%. 相似文献
93.
Measurements of differential capacity vs. potential have been made for a series of s‐triazine herbicides at different concentrations. In all cases the decrease in capacity was independent of the applied potential, so the adsorption is also independent of the potential. From the measurements it can be established that the adsorption follows Langmuir type isotherms. Adsorption constants were obtained for the different herbicides at 25 °C (simetryn, simazine, terburyn and prometon) as well as those to simetryn at different temperatures, from which the adsorption enthalpy of this herbicide was calculated being its value of 17.5 kJ mol?1. 相似文献
94.
Liyuan Zhang Zhenchuan Ma Changyuan Wang Runzhong Yu Dongjie Zhang 《Journal of separation science》2019,42(22):3459-3469
The herbicides in naked oat (Avena nuda L.) samples were extracted, separated, and determined by using ionic‐liquid‐based matrix solid‐phase dispersion‐solvent flotation coupled with high‐performance liquid chromatography. The experimental parameters were optimized and evaluated by a univariate method and orthogonal experiment. A good linear relationship was obtained in the range of 5–5000 µg/kg, and the linear correlation coefficient are between 0.9989~0.9993. The quantification limits for alachlor, metazachlor, propanil, acetochlor, pretilachlor, metolachlor, and butachlor are 5.03, 2.62, 2.73, 4.58, 7.28, 5.05, 5.78 µg/kg, respectively. The average recoveries of the acetanilide herbicides at spiked concentrations of 10, 100, and 500 µg/kg ranged from 92.1 to 104.7%, and relative standard deviations were equal to or lower than 2.9%. 相似文献
95.
H.H. See M. Marsin SanagiWan Aini Wan Ibrahim A.A. Naim 《Journal of chromatography. A》2010,1217(11):1767-1772
A novel microextraction technique termed solid phase membrane tip extraction (SPMTE) was developed. Selected triazine herbicides were employed as model compounds to evaluate the extraction performance and multiwall carbon nanotubes (MWCNTs) were used as the adsorbent enclosed in SPMTE device. The SPMTE procedure was performed in semi-automated dynamic mode and several important extraction parameters were comprehensively optimized. Under the optimum extraction conditions, the method showed good linearity in the range of 1–100 μg/L, acceptable reproducibility (RSD 6–8%, n = 5), low limits of detection (0.2–0.5 μg/L), and satisfactory relative recoveries (95–101%). The SPMTE device could be regenerated and reused up to 15 analyses with no analyte carry-over effects observed. Comparison was made with commercially available solid phase extraction-molecular imprinted polymer cartridge (SPE-MIP) for triazine herbicides as the reference method. The new developed method showed comparable or even better results against reference method and is a simple, feasible, and cost effective microextraction technique. 相似文献
96.
The herbicides amitrole and glyphosate, and its metabolite aminomethyl-phosphonic acid (AMPA), in water samples have been directly analysed by high-performance liquid chromatography using an electrochemical (EC) detector. Limits of detection of 0.3 μg mL−1 for glyphosate, 0.05 μg mL−1 for AMPA and 0.03 μg mL−1 for amitrole were comparable to those obtained by other authors using EC and also by liquid chromatography coupled to mass spectrometry, but the latter method requires derivatisation and pre-concentration of the sample whereas EC methods show similar sensitivity without the need of any derivatisation. The method was specifically designed to analyse extracts from passive samplers used for monitoring of polar herbicide residues in waters. To this purpose, three types of Empore® disks were tested for their ability to adsorb and desorb these ionic, polar analytes. A procedure for their extraction from the membranes and reducing the interferences from other substances present in natural waters (i.e. humic acids) is described. The method is simple, does not require sophisticated equipment and is valid for the analysis and monitoring of herbicides residues using passive samplers. 相似文献
97.
A new solid-phase microextraction (SPME) fiber is fabricated through ultra violet irradiation polymerization of ametryn-molecularly imprinted polymer on the surface of anodized-silylated aluminum wire. The prepared fiber is durable with very good chemical and thermal stability which can be coupled to GC and GC/MS. The effective parameters on the fabrication and application procedures such as spraying mode, ultra violet irradiation (polymerization) time, number of sprayings and polymerizations, pH and ionic strength of sample and extraction time were optimized. This fiber shows high selectivity with great extraction capacity toward triazines. SPME and GC analysis of ametryn, prometryn, terbutryn, atrazine, simazine, propazine and cyanazine using the fabricated fiber result in the detection limits of 9, 32, 27, 43, 51, 74 and 85 ng mL−1, respectively. The reliability of the prepared fiber in real samples has been investigated and proved by using spiked tap water, rice, maize and onion samples. 相似文献
98.
为进一步寻找高效、安全和对环境更加友好的除草剂, 以商品化除草剂单嘧磺酯为研究基础, 对其结构中的苯环5-位取代基作了结构修饰, 合成了26个未见文献报道的新型N-(4'-取代嘧啶-2'-基)-2-甲氧羰基-5-苯甲酰胺基苯磺酰脲化合物, 通过1H NMR、质谱及元素分析确定了化合物的结构. 经油菜平皿法及盆栽法测试了所有化合物的除草活性, 结果表明, 当苯环5-位取代基为苯甲酰胺时, 活性较好, 其对双子叶植物的除草活性与商品化的甲嘧磺隆相当. 相似文献
99.
Ru‐Song Zhao Chun‐Peng Diao Qing‐Feng Chen Xia Wang 《Journal of separation science》2009,32(7):1069-1074
In this paper, solid‐phase extraction (SPE) in combination with dispersive liquid–liquid microextraction (DLLME) has been developed as a sample pretreatment method with high enrichment factors for the sensitive determination of amide herbicides in water samples. In SPE–DLLME, amide herbicides were adsorbed quantitatively from a large volume of aqueous samples (100 mL) onto a multiwalled carbon nanotube adsorbent (100 mg). After elution of the target compounds from the adsorbent with acetone, the DLLME technique was performed on the resulting solution. Finally, the analytes in the extraction solvent were determined by gas chromatography–mass spectrometry. Some important extraction parameters, such as flow rate of sample, breakthrough volume, sample pH, type and volume of the elution solvent, as well as salt addition, were studied and optimized in detail. Under optimum conditions, high enrichment factors ranging from 6593 to 7873 were achieved in less than 10 min. There was linearity over the range of 0.01–10 μg/L with relative standard deviations of 2.6–8.7%. The limits of detection ranged from 0.002 to 0.006 μg/L. The proposed method was used for the analysis of water samples, and satisfactory results were achieved. 相似文献
100.
Encarnación Rodríguez‐Gonzalo Rita Carabias‐Martínez Edith Miranda Cruz Javier Domínguez‐Álvarez Jesús Hernández‐Méndez 《Journal of separation science》2009,32(4):575-584
In the present work we address the development of a simple and effective method for the determination of triazine herbicide residues in horticultural products by CE in nonaqueous media (NACE). Potato samples were selected as a representative matrix of such foods with a nonfatty content. Isolation of the analytes from the sample matrix was accomplished by extraction with organic solvents, assisted by ultrasound; a clean‐up step of the organic extracts was carried out with SPE, using an Oasis MCX® sorbent to retain the analytes directly from the organic medium. The detection limits achieved in spiked potatoes (1.7–4.0 μg/kg) were lower than the default value of maximum residue level (MRL) established by current EU legislation for pesticide residues in foodstuffs. The results obtained were compared with HPLC in order to evaluate the performance of the NACE procedure. 相似文献