色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2014年
3期
299-303
,共5页
离子色谱%紫外检测%碘酸根%碘离子%溴酸根%溴离子%离子液体
離子色譜%紫外檢測%碘痠根%碘離子%溴痠根%溴離子%離子液體
리자색보%자외검측%전산근%전리자%추산근%추리자%리자액체
ion chromatography( IC)%ultraviolet detection( UV)%iodate%iodide%bromate%bromide%ionic liquid
建立了同时分析碘酸根、碘离子、溴酸根和溴离子的离子色谱-紫外检测分析方法。用季铵型阴离子交换柱,以柠檬酸-乙腈为流动相,采用紫外检测器实现了4种离子的同时分离和检测。研究了检测波长和流动相种类、浓度、pH 值等因素对4种离子分离和测定的影响,探讨了保留规律,优化了色谱分析条件。在检测波长为210 nm、流动相为1.0 mmol / L 柠檬酸-乙腈(85:15,v / v;pH 5.0)、流速为0.9 mL / min、柱温为40℃条件下,4种离子完全分离,且系统峰不干扰测定。4种离子的检出限(S / N =3)为0.07~0.16 mg / L,连续5次进样测定的峰面积和保留时间的相对标准偏差均在1%以下。将此方法用于离子液体样品及地下水样品的分析,结果准确、可靠。
建立瞭同時分析碘痠根、碘離子、溴痠根和溴離子的離子色譜-紫外檢測分析方法。用季銨型陰離子交換柱,以檸檬痠-乙腈為流動相,採用紫外檢測器實現瞭4種離子的同時分離和檢測。研究瞭檢測波長和流動相種類、濃度、pH 值等因素對4種離子分離和測定的影響,探討瞭保留規律,優化瞭色譜分析條件。在檢測波長為210 nm、流動相為1.0 mmol / L 檸檬痠-乙腈(85:15,v / v;pH 5.0)、流速為0.9 mL / min、柱溫為40℃條件下,4種離子完全分離,且繫統峰不榦擾測定。4種離子的檢齣限(S / N =3)為0.07~0.16 mg / L,連續5次進樣測定的峰麵積和保留時間的相對標準偏差均在1%以下。將此方法用于離子液體樣品及地下水樣品的分析,結果準確、可靠。
건립료동시분석전산근、전리자、추산근화추리자적리자색보-자외검측분석방법。용계안형음리자교환주,이저몽산-을정위류동상,채용자외검측기실현료4충리자적동시분리화검측。연구료검측파장화류동상충류、농도、pH 치등인소대4충리자분리화측정적영향,탐토료보류규률,우화료색보분석조건。재검측파장위210 nm、류동상위1.0 mmol / L 저몽산-을정(85:15,v / v;pH 5.0)、류속위0.9 mL / min、주온위40℃조건하,4충리자완전분리,차계통봉불간우측정。4충리자적검출한(S / N =3)위0.07~0.16 mg / L,련속5차진양측정적봉면적화보류시간적상대표준편차균재1%이하。장차방법용우리자액체양품급지하수양품적분석,결과준학、가고。
An analytical method of ion chromatography with ultraviolet detection has been developed and applied for the simultaneous determination of iodate,iodide,bromate and bro-mide. The separation was performed on a quaternary ammonium type anion exchange column with citric acid and acetonitrile as mobile phase. The effects of the detection wavelength,the kind and concentration of the mobile phase and other parameters on separation and detection of the four ions were investigated. The retention rules were studied and the chromatographic con-ditions were optimized. Under the conditions of 210 nm as detection wavelength,0. 9 mL / min as flow rate,40 ℃ as column temperature,and 1. 0 mmol / L citric acid-acetonitrile(85 :15,v /v;pH 5. 0)as mobile phase,the four ions were completely separated and the system peaks and other common anions didn’t interfere with the determination. The detection limits of the four ions(S / N = 3)were 0. 07 - 0. 16 mg / L. The relative standard deviations of the retention times and peak areas obtained by determining samples five times continuously were below 1% . The spiked recoveries of the four anions were from 98. 0% to 102% . This method has been success-fully used to determine ionic liquids synthesized by chemistry laboratory and underground water samples. The results were accurate and reliable.