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Permeative Amine Introduction for Very Weak Acid Detection in Ion Chromatography

机译:离子色谱中极弱酸检测的渗透胺介绍

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A permeative amine introduction device (PAID) is placed after a conventional KOH eluent-suppressed conductometric anion chromatography (SCAC) system. The PAID converts the suppressed eluites from the acid form to the corresponding ammonium salt (NR2H + HX -> NR2H2+ + X-) and allows very weak acids HX (pK(a) >= 7.0) that cannot normally be detected by SCAC to be measured by a second conductivity detector following the PAID. Permeative reagent introduction is dilutionless, can be operated without pumps, and provides good mixing (baseline noise 0.8 nS/cm for 27 mu M diethylamine) with low band dispersion (as small as 30 mu L). Diethylamine (DEA) was chosen as the amine source due to its low pK(b) value (3.0), high vapor pressure, low toxicity, and low odor. The eluites are thus detected against a low diethylammonium hydroxide (DEAOH) background (5-31 mu S/cm) as negative peaks because the equivalent conductance of OH- is greater than that of X-. Reducing the background DEA concentration enhances the detectability of traces of weak acids. Lower background [DEA] will limit the maximum concentration of analyte acids that can be determined; a general concept of peak width measurement at a fixed height is proposed as a solution. Trace impurities formed during electrodialytic suppression play a role in background noise; for the first time, we look at the nature of such impurities. The appearance of silicate in a sample put in a glass container as a function of pH can be readily followed. The maximum silica level in high purity type 1 water is 50 nM (1.40 mu g/L Si), which is a measurement challenge in particular. A large injection volume (1 mL) permits detection limits of 21 nM silicate, 3 nM taurine, 3 nM sulfide, and 13 nM cyanide.
机译:在常规KOH洗脱液抑制的电导阴离子色谱(SCAC)系统之后放置一个渗透性胺引入装置(PAID)。 PAID将抑制的洗脱液从酸形式转化为相应的铵盐(NR2H + HX-> NR2H2 + + X-),并允许非常弱的酸HX(pK(a)> = 7.0)被SCAC检测到。在PAID之后由第二个电导检测器测量。渗透试剂的引入是无稀释的,无需泵即可操作,并提供了良好的混合效果(27μM二乙胺的基线噪音为0.8 nS / cm),且带分散度低(小至30μL)。二乙胺(DEA)因其低pK(b)值(3.0),高蒸气压,低毒性和低气味而被选为胺源。因此,在低的二乙基氢氧化铵(DEAOH)背景(5-31μS / cm)上检测到洗脱液为负峰,因为OH-的等效电导大于X-。降低背景DEA浓度可增强痕量弱酸的可检测性。较低的本底[DEA]将限制可以测定的分析物酸的最大浓度。提出了在固定高度处测量峰宽的一般概念作为解决方案。电渗析抑制过程中形成的痕量杂质在背景噪声中起作用。第一次,我们看看这种杂质的性质。可以容易地观察放入玻璃容器中的样品中硅酸盐随p​​H的变化。高纯度1型水中的最大二氧化硅含量为50 nM(1.40μg / L Si),这尤其是测量上的挑战。大进样量(1 mL)允许检测限为21 nM硅酸盐,3 nM牛磺酸,3 nM硫化物和13 nM氰化物。

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