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[求助]
查查这篇文章是否SCI检索了，检索号是多少？谢谢！
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IL-USA-DLLME method used to simultaneously extract and determine four phenylurea herbicides in water samples，Current Analytical Chemistry，2011 7 ( 4): 357-364 万分火急 |
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逐月8815
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【答案】应助回帖
感谢参与，应助指数 +1
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可以见所得到了，检索号好像要检索机构出具的。 这是全部检索内容 IL-USA-DLLME Method to Simultaneously Extract and Determine Four Phenylurea Herbicides in Water Samples 作者: Wang, SL (Wang, Suli)1,2; Liu, CY (Liu, Congyun)1; Liu, FM (Liu, Fengmao)1; Ren, LP (Ren, Liping)1 来源出版物: CURRENT ANALYTICAL CHEMISTRY 卷: 7 期: 4 页: 357-364 出版年: OCT 2011 被引频次: 0 (来自 Web of Science) 引用的参考文献: 34 [ 查看 Related Records ] 引证关系图 摘要: An ionic-liquid ultrasound-assisted dispersive liquid-liquid microextraction method (IL-USA-DLLME) was introduced to determine four phenylurea herbicides (i.e., isoproturon, monolinuron, linuron, and diuron) in water samples with high performance liquid chromatography (HPLC). The ionic liquid of 1-hexyl-3-methylimidazolium hexafluorophosphate [HMIMPF6] was dispersed into the aqueous sample solution in fine droplets by ultrasound and was used as the extraction solvent; the phenylurea herbicides were concentrated into the ionic liquid phase. The extraction conditions, such as the volume of the extraction solvent, sonication and centrifugation time, ionic strength, and the emulsification-extraction temperature, were optimized. Under the optimized conditions, the linear correlation coefficient ranged from 0.9954 to 0.9969 for concentration levels of 2-100 mu gL(-1). The good recovery (68-100%) of target analytes was obtained from the water samples. The relative standard deviations (RSDs, n=6) ranged from 2.3-9.5%, and the limits of detection (LODs) for the herbicides were between 0.10 mu gL(-1) and 0.24 mu gL(-1). The applicability of the proposed method was evaluated by the extraction and determination of phenylurea herbicides from several natural water samples. 入藏号: WOS:000300354500011 文献类型: Article 语种: English 作者关键词: IL-USA-DLLME; Phenylurea herbicides; Water samples; HPLC KeyWords Plus: LIQUID-LIQUID MICROEXTRACTION; ULTRASOUND-ASSISTED EMULSIFICATION; ATOMIC-ABSORPTION-SPECTROMETRY; POLYCYCLIC AROMATIC-HYDROCARBONS; CHROMATOGRAPHY-MASS SPECTROMETRY; SOLID-PHASE MICROEXTRACTION; GAS-CHROMATOGRAPHY; ORGANOPHOSPHORUS PESTICIDES; FLAME RETARDANTS; SENSITIVE METHOD 通讯作者地址: Liu, FM (通讯作者),China Agr Univ, Beijing 100193, Peoples R China 地址: 1. China Agr Univ, Beijing 100193, Peoples R China 2. Hebei North Univ, Zhangjiakou 075131, Peoples R China 电子邮件地址: lfm2000@cau.edu.cn 基金资助致谢: 基金资助机构 授权号 40th Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry Natural Science Foundation of Hebei Province B2011405007 [显示基金资助信息][隐藏基金资助信息] The authors acknowledge the financial support from the 40th Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry and the Natural Science Foundation of Hebei Province (No. B2011405007). 出版商: BENTHAM SCIENCE PUBL LTD, EXECUTIVE STE Y26, PO BOX 7917, SAIF ZONE, 1200 BR SHARJAH, U ARAB EMIRATES Web of Science 分类: Chemistry, Analytical 学科类别: Chemistry IDS 号: 893KJ ISSN: 1573-4110 |
4楼2012-03-26 09:08:18
wanyue1111
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2楼2012-03-26 08:59:26
【答案】应助回帖
感谢参与，应助指数 +1
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FN Thomson Reuters Web of Knowledge VR 1.0 PT J AU Wang, SL Liu, CY Liu, FM Ren, LP AF Wang, Suli Liu, Congyun Liu, Fengmao Ren, Liping TI IL-USA-DLLME Method to Simultaneously Extract and Determine Four Phenylurea Herbicides in Water Samples SO CURRENT ANALYTICAL CHEMISTRY LA English DT Article DE IL-USA-DLLME; Phenylurea herbicides; Water samples; HPLC ID LIQUID-LIQUID MICROEXTRACTION; ULTRASOUND-ASSISTED EMULSIFICATION; ATOMIC-ABSORPTION-SPECTROMETRY; POLYCYCLIC AROMATIC-HYDROCARBONS; CHROMATOGRAPHY-MASS SPECTROMETRY; SOLID-PHASE MICROEXTRACTION; GAS-CHROMATOGRAPHY; ORGANOPHOSPHORUS PESTICIDES; FLAME RETARDANTS; SENSITIVE METHOD AB An ionic-liquid ultrasound-assisted dispersive liquid-liquid microextraction method (IL-USA-DLLME) was introduced to determine four phenylurea herbicides (i.e., isoproturon, monolinuron, linuron, and diuron) in water samples with high performance liquid chromatography (HPLC). The ionic liquid of 1-hexyl-3-methylimidazolium hexafluorophosphate [HMIMPF6] was dispersed into the aqueous sample solution in fine droplets by ultrasound and was used as the extraction solvent; the phenylurea herbicides were concentrated into the ionic liquid phase. The extraction conditions, such as the volume of the extraction solvent, sonication and centrifugation time, ionic strength, and the emulsification-extraction temperature, were optimized. Under the optimized conditions, the linear correlation coefficient ranged from 0.9954 to 0.9969 for concentration levels of 2-100 mu gL(-1). The good recovery (68-100%) of target analytes was obtained from the water samples. The relative standard deviations (RSDs, n=6) ranged from 2.3-9.5%, and the limits of detection (LODs) for the herbicides were between 0.10 mu gL(-1) and 0.24 mu gL(-1). The applicability of the proposed method was evaluated by the extraction and determination of phenylurea herbicides from several natural water samples. C1 [Wang, Suli; Liu, Congyun; Liu, Fengmao; Ren, Liping] China Agr Univ, Beijing 100193, Peoples R China. [Wang, Suli] Hebei North Univ, Zhangjiakou 075131, Peoples R China. RP Liu, FM (reprint author), China Agr Univ, Beijing 100193, Peoples R China EM lfm2000@cau.edu.cn FU 40th Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry; Natural Science Foundation of Hebei Province[B2011405007] FX The authors acknowledge the financial support from the 40th Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry and the Natural Science Foundation of Hebei Province (No. B2011405007). NR 34 TC 0 Z9 0 PU BENTHAM SCIENCE PUBL LTD PI SHARJAH PA EXECUTIVE STE Y26, PO BOX 7917, SAIF ZONE, 1200 BR SHARJAH, U ARAB EMIRATES SN 1573-4110 J9 CURR ANAL CHEM JI Curr. Anal. Chem. PD OCT PY 2011 VL 7 IS 4 BP 357 EP 364 PG 8 WC Chemistry, Analytical SC Chemistry GA 893KJ UT WOS:000300354500011 ER -------------------------------------------------------------------------------- EF |
3楼2012-03-26 09:00:58
5楼2012-03-26 09:09:33
