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国家自然科学基金(20911140271)

作品数:3 被引量:20H指数:2
相关作者:王丽丽朱岩诸寅更多>>
相关机构:浙江工业大学浙江大学更多>>
发文基金:国家自然科学基金浙江省自然科学基金更多>>
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液相微萃取-离子色谱法测定污水中痕量芳香胺被引量:18
2012年
基于中空纤维液相微萃取技术,建立了污水中两种痕量芳香胺类物质(邻甲苯胺和对氯苯胺)的离子色谱分析方法。对中空纤维液相微萃取条件进行了优化,得到的优化条件为:以正辛醇为萃取溶剂,供体相中NaOH的浓度为0.01 mol/L,NaCl的质量浓度为500 g/L,接收相中HCl的浓度为0.1 mol/L,搅拌速度为430 r/min,萃取时间为30 min。在优化条件下,邻甲苯胺的富集倍数为88倍,对氯苯胺的富集倍数为124倍。供体相中邻甲苯胺和对氯苯胺的质量浓度在0.005~0.1 mg/L范围内呈良好的线性,相关系数为0.999 8~0.999 9,检出限(以3倍信噪比计)分别为0.2和0.5μg/L,5次测定0.01 mg/L的混合标准溶液的相对标准偏差分别为0.85%和3.38%。该方法操作简单,环境友好,提高了离子色谱检测芳香胺类物质的灵敏度。
诸寅朱岩王丽丽
关键词:液相微萃取中空纤维离子色谱芳香胺
Electrocatalytic response of poly(cobalt tetraaminophthalocyanine)/multi-walled carbon nanotubes-Nafion modified electrode toward sulfadiazine in urine被引量:2
2012年
A highly sensitive amperometric sulfadiazine sensor fabricated by electrochemical deposition of poly(cobalt tetraaminophthalocyanine) (poly(Co II TAPc)) on the surface of a multi-walled carbon nanotubes-Nafion (MWCNTs-Nafion) modified electrode is described.This electrode showed a very attractive performance by combining the advantages of Co II TAPc,MWCNTs,and Nafion.Compared with the bare glassy carbon electrode (GCE) and the MWCNTs-Nafion modified electrode,the electrocatalytic activity of poly(Co II TAPc)-coated MWCNTs-Nafion GCE generated greatly improved electrochemical detections toward sulfadiazine including low oxidation potential,high current responses,and good anti-fouling performance.The oxidation peak currents of sulfadiazine obtained on the new modified electrode increased linearly while increasing the concentration of sulfadiazine from 0.5 to 43.5 μmol/L with the detection limit of 0.17 μmol/L.
Xiao-ping HONGYan ZHUYan-zhen ZHANG
关键词:SULFADIAZINE
Determination of lisinopril using anion exchange chromatography with integrated pulsed amperometric detection
2012年
A rapid and practical method for direct detection of lisinopril in anion exchange chromatography(AEC) has been developed with integrated pulsed amperometric detection(IPAD).Dionex AS 18(250 mm×2 mm) and AG 18(50 mm×2 mm) columns and 40 mmol/L NaOH solution were used for separation.Multi-step potential waveform parameters were optimized to maximize the signal-to-noise ratio(S/N).Utilizing the optimized waveform,the repeatability(intra-day) precision and intermediate(inter-day) precision were obtained with relative standard deviation(RSD) of 0.74,0.93,respectively.The limit of quantification(LOQ) and limit of detection(LOD) were found to be 0.37,0.12ng/mL,respectively,with the correlation coefficient of 0.9998 over concentration range 0.01-1μg/mL.The present method was successfully applied to the determination of lisinopril in human plasma.The recoveries of plasma sample spiked by 0.2μg/mL,0.8μg/mL lisinopril were 98.31-103.23%with RSD of 1.41%, 0.61%,respectively.
Yu Xiu LiuDan ShouMei Lan ChenZhi Dong ChenPei Min ZhangYan Zhu
关键词:LISINOPRILPLASMA
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