Related Experiment Video
Updated: Mar 26, 2026

Determination of the Gas-phase Acidities of Oligopeptides
Published on: June 24, 2013
Permeative Amine Introduction for Very Weak Acid Detection in Ion Chromatography
Hongzhu Liao1, Purnendu K Dasgupta1
1Department of Chemistry and Biochemistry, University of Texas at Arlington , Arlington, Texas 76019-0065, United States.
Abstract:
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 (pKa ≥ 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 μM diethylamine) with low band dispersion (as small as 30 μL). Diethylamine (DEA) was chosen as the amine source due to its low pKb 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 μS/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 μg/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.
More Related Videos
08:56Detection of Regulated Ergot Alkaloids in Food Matrices by Liquid Chromatography-Trapped Ion Mobility Spectrometry-Time-of-Flight Mass Spectrometry
Published on: November 22, 2024
09:46Qualitative Identification of Carboxylic Acids, Boronic Acids, and Amines Using Cruciform Fluorophores
Published on: August 19, 2013
Related Concept Videos
Ion-Exchange Chromatography
Basicity of Heterocyclic Aromatic Amines
Titration of a Weak Base with a Strong Acid
Using the ICE table and substituting the Kb value, we calculate the initial pH of 50 mL of 0.1 M ammonia to be 11.11. Addition of 25 mL of 0.1 M hydrochloric acid to this solution of ammonia results in a buffer with an equal concentration of ammonia and ammonium ions. The pH of this buffer can be calculated by substituting these...
High-Performance Liquid Chromatography: Types of Detectors
Mass Spectrometry of Amines
Titration in Nonaqueous Solvents