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Ion chromatographic method for the determination of cations of group IA and IIA in water samples, pharmaceuticals and energy drinks by non-suppressed conductometric detection

机译:非抑制电导检测用离子色谱法测定水样,药品和能量饮料中IA和IIA组阳离子

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An efficient ion chromatographic (IC) method was developed for the simultaneous quantitative determination of Li+, Na+, NH4+, K+, Cs+, Ca2+, Mg2+, Sr2+, Ba2+ and Be2+ in energy drinks, pharmaceutical and drinking water samples by non-suppressed conductometric detection. The separation of ten cations including ammonium was achieved using a cation-exchange column and low conductivity mobile phase. The mobile phase consisted of tartaric acid, dipicolinic acid and boric acid. The separation of the cations was completed in less than 18 min, with a flow rate of 1.2 mL min?1. The separation was not affected by the existence of cations Co2+, Cr3+, Cd2+, Cu2+, Bi3+, Ag+, Fe3+ and Zn2+ in concentrations up to 20 mg L?1. Using an injection volume of 20 μL the obtained detection limits were 0.003 mg L?1, 0.02 mg L?1, 0.01 mg L?1, 0.01 mg L?1, 0.10 mg L?1, 0.01 mg L?1, 0.02 mg L?1, 0.02 mg L?1, 0.003 mg L?1 and 0.1 mg L?1, for Li+, Na+, NH4+, K+, Cs+, Ca2+, Mg2+, Sr2+, Be2+ and Ba2+ respectively. The intra-day repeatability (RSD%, n=5) ranged from 1.1% to 4.8%, and the inter-day (n=5) between 1.8% and 5.4% respectively. The method was applied to the analysis of various bottled and tap water, pharmaceutical preparations and energy drinks commercially available.
机译:建立了一种高效的离子色谱法(IC),用于通过非抑制电导检测同时定量测定能量饮料,药品和饮用水样品中的Li +,Na +,NH4 +,K +,Cs +,Ca2 +,Mg2 +,Sr2 +,Ba2 +和Be2 + 。使用阳离子交换柱和低电导率流动相可分离包括铵在内的十种阳离子。流动相由酒石酸,二吡啶甲酸和硼酸组成。在不到18分钟的时间内完成了阳离子的分离,流速为1.2 mL min?1。浓度不超过20 mg L?1的阳离子Co2 +,Cr3 +,Cd2 +,Cu2 +,Bi3 +,Ag +,Fe3 +和Zn2 +的存在不影响分离。使用20μL的进样量,获得的检出限为0.003 mg L?1、0.02 mg L?1、0.01 mg L?1、0.01 mg L?1、0.10 mg L?1、0.01 mg L?1、0.02 mg对于Li +,Na +,NH 4 +,K +,Cs +,Ca 2+,Mg2 +,Sr2 +,Be2 +和Ba2 +分别为L≤1、0.02 mg L≤1、0.003 mgL≤1和0.1 mgL≤1。日内重复性(RSD%,n = 5)在1.1%至4.8%之间,日间(n = 5)在1.8%和5.4%之间。该方法用于分析各种瓶装和自来水,药物制剂和市售的能量饮料。

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