Optimization of an electrolytic conductivity detector for determination of toxic nitrogen-containing food contaminants separated by open tubular column gas chromatography

The combination of open tubular column gas chromatography with electrolytic conductivity detection has been evaluated for the determination of nitrogen-containing pesticide residues in food extracts. Optimization of the column position at the column-detector interface was crucial to the successful operation of the detector. The signal-to-noise ratio and response stability of the detector are greatly influenced by the composition of the electrolyte solvent. Large volume splitless injections using retention gaps and optimized detector operating conditions enabled pesticide residues in food extracts to be determined at sub parts-per-million levels. Although the electrolytic conductivity detector is less sensitive than the thermionic ionization detector, its greater nitrogen selectivity can he crucial to the determination of nitrogen-containing contaminants in food extracts, particularly in complex mixtures where phosphorus-containing contaminants or matrix compounds are also present.     

Determination of synthetic pharmaceuticals in phytotherapeutics by capillary zone electrophoresis with contactless conductivity detection (CZE-CD)

In this work, a method for simultaneous determination of amfepramone, fenproporex, sibutramine and fluoxetine was developed by capillary zone electrophoresis with capacitively coupled contactless conductivity detection (C⁴D) using a homemade capillary electrophoretic system. The optimized conditions for the separation of the pharmaceuticals by CZE were as follows: 50 mmol L^− 1 phosphate buffer (pH 5.0) in 50/50 (v/v) mixture of water/acetonitrile as the working electrolyte, 15 kV separation voltage, 25 °C separation temperature, hydrodynamic injection by gravity using 20 cm injection height and 60 s injection time. The detection by C⁴D was carried out by using a homemade detector, which employs a sinusoidal wave generator operating at 600 kHz frequency and 2 V_pp wave amplitude. The optimized and validated CZE-C⁴D method was applied for the determination of the studied pharmaceuticals as adulterants in phytotherapeutic formulations commercialized in Brazil for slimming purposes.     

Multi-stage chromatographic procedure for the isolation of a single oligomeric species (vinyl chloride tetramer) from poly(vinyl chloride) resin used for food packaging applications

A multi-stage chromatographic procedure is described whereby low-molecular-weight material initially obtained by soxhlet diethyl ether extraction from food grade poly(vinyl chloride) (PVC) resin, is fractionated to yield firstly a mixture of vinyl chloride oligomers and then a single species free from other impurities. A number of column chromatographic procedures were evaluated, and a combination of high-performance size exclusion columns using initially tetrahydrofuran solvent followed by toluene solvent were shown to produce the most effective separation. The isolation and purification of a vinyl chloride tetramer was monitored by capillary column gas chromatography with specific chlorine detection (Hall electrolytic conductivity detector) and the identification confirmed by mass spectrometry. Using this newly developed procedure 0.5 mg of vinyl chloride tetramer was isolated from a PVC base resin.     

Conductivity monitoring of inorganic anions with a Cu(II)-containing poly(3-methylthiophene) electrode in single-column ion chromatography

An amperometric detector unit equipped with a Cu(II)-containing poly(3-methylthiophene) working electrode is described for the single-column ion chromatographic detection of electroinactive inorganic anions, such as F^?, Cl^?, Br^?, NO₂^? and NO₃^?. Chromatograms obtained with this unit and with a commercial conductivity detector are almost identical with regard to peak height. Thus, an amperometric unit employing this modified electrode can be used as a conductance monitor in ion chromatographic analysis. Although the responses of this electrode seem to be conductivity related, the detection principle is probably based on a dual mechanism involving equilibria between copper ions and various anions of the system in addition to simple conductivity changes associated with the passage of analyte plugs. This explains the difference in responses observed with platinum and stainless-steel electrodes used in the same cell configuration. The detector displays a linear range of at least two orders of magnitude on a logarithmic scale.     

Dual fluorescence/contactless conductivity detection for microfluidic chip

A new dual detection system for microchip is reported. Both fluorescence detector (FD) and contactless conductivity detector (CCD) were combined together and integrated on a microfluidic chip. They shared a common detection position and responded simultaneously. A blue light-emitting diode was used as excitation source and a small planar photodiode was used to collect the emitted fluorescence in fluorescence detection, which made the device more compact and portable. The coupling of the fluorescence and contactless conductivity modes at the same position of a single separation channel enhanced the detection characterization of sample and offered simultaneous detection information of both fluorescent and charged specimen. The detection conditions of the system were optimized. K⁺, Na⁺, fluorescein sodium, fluorescein isothiocyanate (FITC) and FITC-labeled amino acids were used to evaluate the performance of the dual detection system. The limits of detection (LOD) of FD for fluorescein Na⁺, FITC, FITC-labeled arginine (Arg), glycine (Gly) and phenylalanine (Phe) were 0.02 μmol L⁻¹, 0.05 μmol L⁻¹, 0.16 μmol L⁻¹, 0.15 μmol L⁻¹, 0.12 μmol L⁻¹ respectively, and the limits of detection (LOD) of CCD achieved 0.58 μmol L⁻¹ and 0.39 μmol L⁻¹ for K⁺ and Na⁺ respectively.     

On-line purge and trap gas chromatography for monitoring of trihalomethanes in drinking water distribution systems

A method using an automated on-line purge and trap gas chromatograph with a dry electrolytic conductivity detector (DELCD) has been developed for monitoring four regulated trihalomethanes in drinking water distribution systems. This analyzer samples trihalomethanes from drinking water by pervaporation through a silicone capillary membrane contained within a gas extraction cell (GEC) followed by preconcentration using an adsorbent trap. Trihalomethanes are subsequently desorbed from the trap onto a capillary column, separated and detected. The analyzer operates in real-time, samples directly from the drinking water distribution system and is fully automated. The optimization, operation, and evaluation of the analyzer and method are discussed. Method detection limits (MDL) are less than 1.0 μg L⁻¹ with acceptable estimates for accuracy, and precision. The results from two on-line monitoring studies in chlorinated and chloraminated distribution systems are presented. The performance of the method is compared directly to United Stated Environmental Protection Agency Method 502.2 and shows a very slight, but acceptable bias.     

Gas Liquid Chromatographic Determination of Promethazine Hydrochloride in Polyethylene Glycol Suppositories Using the Hall's Electrolytic Conductivity Detector

Abstract

A gas liquid chromatographic method using the Hall's electrolytic conductivity detector is described for the determination of promethazine hydrochloride in polyethylene glycol suppositories. This method is capable of distinguishing the intact drug from its thermal degradation products. A linear relationship between peak height ratio (promethazine/promazine) and promethazine hydrochloride concentration is found up to a concentration of 600 μg/ml. In the presence and absence of polyethylene glycol vehicle the recovery of promethazine hydrochloride is found to be 100.2 and 99.7 percent respectively. The percent coefficient of variation is 0.62 and 0.94 in the absence and presence of polyethylene glycol vehicle.     

Electrophoretic microchip with dual-opposite injection for simultaneous measurements of anions and cations

A novel dual-injection poly(methylmethacrylate) (PMMA) microchip electrophoretic system has been designed and fabricated for simultaneous measurements of anions and cations using a single channel and detection device. It consists of two sample reservoirs, on both sides of a common separation channel. Anions and cations can be simultaneously electrokinetically injected into both ends of the separation channel. Due to lower electroosmotic flow in polymer channels compared to glass ones, the cations and anions migrate in opposite directions and can be separated from each other and detected using a movable contactless conductivity detector (MCCD) positioned around the center of the separation channel. The effects of the detector position and of the separation voltage on the response and resolution have been studied and optimized for simultaneous determination of six low-energy explosive-related ions, including ammonium, methyl ammonium, sodium, chloride, nitrate, and perchlorate in a single analytical run (of ca. 3 min). Simultaneous detection of nerve-agent degradation products along with explosive-related anions and cations is also demonstrated. The versatile system can also be used for separately measuring anions or cations. The attractive behavior of the dual-opposite injection microchip offers great promise for a wide range of applications, including "total ion analysis" of various samples.     

Chlorine-Selective Detection in Supercritical Fluid Chromatography using a Coulson Electrolytic Conductivity Detector

Abstract

A Coulson electrolytic conductivity detector has been coupled successfully to a supercritical fluid chromatograph, providing chlorine-selective detection. This involves minimal modification of the detector and no modification of the SFC or its operation. The general operating parameters of the SFC/CECD system were established by direct injection of three probe compounds: chlordane, γ-lindane, and hexachlorobenzene. Next, the SFC separation of a test mixture containing phenol, γ-lindane, and several chlorinated phenols and related compounds was optimized using UV-Vis and FID detection. The mixture was then separated using the same chromatographic method but with the CECD in line with the UV-Vis detector. The response of the CECD was linear and selective for chlorinated compounds. Limits of detection for the test mixture by CECD ranged from 80 – 250 ng/μL, corresponding to approximately 14 – 44 ng of chlorine on column, and were dependent on chromatographic conditions, but independent of analyte structure.     

Determination of organotin compounds (OTC) at low levels in seawater by solid-phase extraction (SPE) and gas chromatography-pulsed flame photometric detection (GC-PFPD)

In this work, a simple, sensitive and affordable analytical method for the simultaneous determination of nine organotin compounds (butyltins, phenyltins and methyltins) in seawater using solid-phase extraction (SPE) and gas chromatography-pulsed flame photometric detection was developed and validated. The performance of three different SPE cartridges (Envi C₁₈, Oasis HLB and Oasis MCX) and three elution solvents of different polarity (hexane, methanol and acetonitrile) was evaluated. The extraction parameters, such as solvent volume, presence of complexing and ion-pairing reagents, sample volume and pH and breakthrough volume, were also investigated. Tributyltin, as the organotin compound of special interest, was efficiently extracted using any of the cartridges and solvents tested. However, the simultaneous extraction of all nine organotin compounds was the most efficient using reversed-phase Envi C₁₈ cartridge and 0.1% (w/v) tropolone in methanol as eluent. The optimised method resulted in good recovery, precision and linearity for all compounds, particularly for tri- and disubstituted species. Method detection limits ranged from 0.22 to 1.27 ng(Sn) L^?1 for butyltins, 0.37 to 4.91 ng(Sn) L^?1 for phenyltins and 0.45 to 1.16 ng(Sn) L^?1 for methyltins. The accuracy of butyltins determination was further verified by the comparison with purchased derivatised standards. The developed method was successfully applied to the environmental samples.     

Evaluation and comparison of selective gas chromatographic detectors for the analysis of pesticide residues

Summary A series of studies is described on the evaluation and comparison of some selective gas chromatographic detectors used in pesticide residue analysis. A detailed study of the optimization and response characteristics of the CsBr and RbCl three-electrode alkali flame ionization detector for N and P compounds, the Coulson electrolytic conductivity detector in the nitrogen, sulphur and pyrolytic modes of operation and the sulphur phosphorus emission detector, a type of flame photometric detector, was carried out to obtain maximum sensitivity and reliability for the analysis of pesticide residues in various biological substrates. It was observed that the alkali flame and electrolytic conductivity detector responses to nitrogen compounds were of the same order, while the electrolytic conductivity detector was more sensitive than the flame photometric detector to sulphur compounds. Also, attempts were made to correlate the responses from these different detector systems using the insecticide chlorpyrifos which contains P, S, Cl and N atoms. The use of chlorpyrifos as an evaluation standard in verifying the acceptable performance of these types of detectors is recommended.Chemistry and Biology Research Institute Contribution No 901     

Detection limits of thermal conductivity and photoionization detectors in high speed narrow bore CGC

Not only the required input band width and the availability of compatible instrumentation limit the reduction of column diameter but so do the column sample capacity and detector characteristics, such as volume and sensitivity. In this paper the scope and limitations of thermal conductivity and photoionization detection at atmospheric and reduced pressures for capillary gas chromatography are discussed at length. It is shown that the sensitivity of a thermal conductivity detector is inversely proportional to the pressure. Reduction of cell volume and decrease of pressure appear equivalent with respect to minimum detectable amount and peak broadening. This results in femtogram detection limits for column diameters as low as 10 μm. For photoionization detectors the sensitivity did not improve at reduced pressures, so that the effect of reduced pressure and addition of make-up gas on the detection limits is the same. Nevertheless, the applicability of a low volume photoionization detector (40 μl) for capillary columns with a diameter as low as 50 μm will be demonstrated by series coupled PID and FID detectors and illustrated with various applications.     

Pulsed discharge detector: theory and applications

The pulsed discharge detector (PDD) is a significant advancement in gas chromatography (GC) detector design which can be operated in three different modes: pulsed discharge helium ionization (He-PDPID), pulsed discharge electron capture (PDECD) and helium ionization emission (PDED). The He-PDPID can detect permanent gases, volatile inorganics and other compounds which give little or no response with the flame ionization detector (FID) and has significantly better limits of detection (minimum detectable quantities (MDQs) in low picogram range) than can be achieved with a thermal conductivity detector (typically not lower than 1 ng). The PDECD has similar or better sensitivity (MDQs of 10(-15) to 10(-12) g) than radioactive source ECD but does not require licensing, wipe tests and other administrative or safety requirements which have increased over security concerns. The PDED shows promise as an extremely selective and sensitive elemental detector but a commercial unit is not presently available. In this report, the theory of operation, applications of the PDD and the practical aspects of using this novel detector are presented.     

Utilizing two detectors in the measurement of trichloroacetic acid in human urine by reaction headspace gas chromatography

A reaction headspace gas chromatography (HS‐GC) technique was investigated for quantitatively analyzing trichloroacetic acid in human urine. This method is based on the decomposition reaction of trichloroacetic acid under high‐temperature conditions. The carbon dioxide and chloroform formed from the decomposition reaction can be respectively detected by the thermal conductivity detection HS‐GC and flame ionization detection HS‐GC. The reaction can be completed in 60 min at 90°C. This method was used to quantify 25 different human urine samples, which had a range of trichloroacetic acid from 0.52 to 3.47 mg/L. It also utilized two different detectors, the thermal conductivity detector and the flame ionization detector. The present reaction HS‐GC method is accurate, reliable and well suitable for batch detection of trichloroacetic acid in human urine.     

Indirect hydrogen analysis by gas chromatography coupled to mass spectrometry (GC–MS)

Gas chromatography (GC) is an analytical tool very useful to investigate the composition of gaseous mixtures. The different gases are separated by specific columns but, if hydrogen (H₂) is present in the sample, its detection can be performed by a thermal conductivity detector or a helium ionization detector. Indeed, coupled to GC, no other detector can perform this detection except the expensive atomic emission detector. Based on the detection and analysis of H₂ isotopes by low‐pressure chemical ionization mass spectrometry (MS), a new method for H₂ detection by GC coupled to MS with an electron ionization ion source and a quadrupole analyser is presented. The presence of H₂ in a gaseous mixture could easily be put in evidence by the monitoring of the molecular ion of the protonated carrier gas. Copyright © 2013 John Wiley & Sons, Ltd.     

A capillary electrophoresis system with dual capacitively coupled contactless conductivity detection and electrospray ionization tandem mass spectrometry

A commercial system that is comprised of a CE coupled to an ESI triple quadrupole mass spectrometer was equipped with two capacitively coupled contactless conductivity detectors (C⁴Ds). The first C⁴D was positioned inside the original cartridge, and the second C⁴D was positioned as close as possible to the ESI probe entrance by using a 3D‐printed support. The C⁴Ds electropherograms were matched to the ESI‐MS electropherogram by correcting their timescales by the factor L_T/L_D, where L_T and L_D are the total capillary length and the length until the C⁴D, respectively. A general approach for method development supporting the simultaneous conductivity and MS detection is discussed, while application examples are introduced. These examples include the use of C⁴D as a simple device that dismiss the use of an EOF marker, a low‐selectivity detector that continuously provide information about unexpected features of the sample, and even a detector that can be more sensitive than ESI‐MS. The C⁴D used in this setup proved to have a smaller contribution to the peak broadening than ESI‐MS, which allowed that a C⁴D, positioned at 12 cm from the inlet of an 80‐cm‐long capillary, could be used to foresee position and shape of the peaks being formed 6.8 times slower at the ESI‐MS electropherogram.     

High-performance liquid chromatography of biphenols and bis (hydroxyphenyl) propanes (dianes) with voltammetric and UV photometric detection

Summary The retention behaviour of mono- and dihydroxy derivatives of biphenol and bis(hydroxyphenyl)propanes was studied on chemically bonded C-18, CN-, phenyl, phenoxypropyl- and NH₂ stationary phases and on silica gel. The effects of the mobile phase, i.e., of the methanol content, the ionic strength, pH and the contents of cationic and anionic ion-pairing agents on the retention data were investigated. In the reversed-phase systems, all the substances are satisfactorily separated except for 3- and 4-hydroxybiphenyl; these isomers can be separated on silica gel, using a mixture of heptane and propanol as the mobile phase. Sodium dodecylsulphate, present at concentrations higher than the critical micelle concentration (about 10⁻² M, depending on the methanol content), causes a decrease in the retention times and an improvement in the separation. UV absorption spectra, calibration curves and the detection limit values were obtained at two wavelengths and at various salt concentrations in the mobile phase. Hydrodynamic voltammograms of the solutes were measured in a carbon fibre detector and the calibration curves and detection limit values were measured at the optimal voltage (+1.2 V/Ag/AgCl) as a function of the mobile phase composition. For most test substances voltammetric detection is two to three times more sensitive than UV detection. The combination of a UV and a voltammetric detector in series has been utilized to identify the products of microbial degradation of biphenyl.     

A methodological study of mercury speciation using Dogfish liver CRM (DOLT-2)

The purpose of the study was to optimise analytical methods for determination of the chemical speciation of mercury in studies of protective mechanisms of selenium. Optimisation of the methods was performed using CRM DOLT-2 (Dogfish liver), both in its original form and after separation of various fractions. The sample was homogenised with 10 mM Tris-HCl buffer (pH 7.6) and ultracentrifuged. The soluble phase obtained was applied to a size exclusion chromatography column (Sephadex ¶G-75 column) for separation of various protein fractions. Total mercury (total Hg), monomethyl mercury (MeHg) and selenium (Se) were determined in whole dogfish liver tissue and its soluble and insoluble phases (pellet). Different approaches for determination of total Hg and MeHg were compared. Simultaneous determination of MeHg and inorganic mercury (Hg²⁺) was based on alkaline dissolution and/or acid leaching, followed by ethylation, room temperature precollection, isothermal gas chromatography (GC), pyrolysis and detection with cold vapour atomic fluorescence spectrometry (CVAFS). The sum of MeHg and Hg²⁺ was compared to total Hg results obtained by acid digestion and CVAAS detection. The accuracy of MeHg determination was checked by its determination using acid leaching at room temperature, solvent extraction, back extraction into Milli-Q water, ethylation, GC and CVAFS detection. For the insoluble phase it is recommended to use solvent extraction for MeHg and acid digestion CVAAS for total Hg. For determination of MeHg and Hg²⁺ in the lyophilised sample and water soluble fractions containing low concentrations of mercury species, the simultaneous measurement of MeHg and Hg²⁺ after alkaline dissolution is the most appropriate method.     

Determination of trihalomethanes in water samples: a review

This article reviews the most recent literature addressing the analytical methods applied for trihalomethanes (THMs) determination in water samples. This analysis is usually performed with gas chromatography (GC) combined with a preconcentration step. The detectors most widely used in this type of analyses are mass spectrometers (MS) and electron capture detectors (ECD). Here, we review the analytical characteristics, the time required for analysis, and the simplicity of the optimised methods. The main difference between these methods lies in the sample pretreatment step; therefore, special emphasis is placed on this aspect. The techniques covered are direct aqueous injection (DAI), liquid-liquid extraction (LLE), headspace (HS), and membrane-based techniques. We also review the main chromatographic columns employed and consider novel aspects of chromatographic analysis, such as the use of fast gas chromatography (FGC). Concerning the detection step, besides the common techniques, the use of uncommon detectors such as fluorescence detector, pulsed discharge photoionization detector (PDPID), dry electrolytic conductivity detector (DELCD), atomic emission detector (AED) and inductively coupled plasma-mass spectrometry (ICP-MS) for this type of analysis is described.     

Electroanalytical Determination of Cd(II) and Pb(II) in Bivalve Mollusks using Electrochemically Reduced Graphene Oxide‐based Electrode

An electrochemical sensor for the simultaneous determination of Cd(II) and Pb(II) by square wave anodic stripping voltammetry (SWASV) in bivalve mollusks using a glassy carbon electrode modified with electrochemically reduced graphene oxide has been developed. The modified surface was characterized by cyclic voltammetry, high resolution scanning electron microscopy (HR‐SEM), and Raman spectroscopy. The optimum conditions were optimized and a linear range was observed from 15–105 μg L^?1 with a limits of detection of 15 μg L^?1 for Cd(II) and Pb(II). The methodology was validated and applied in different samples of commercial bivalve mollusks with satisfactory results. The high conductivity and greater surface area of the modifying agent improves the preconcentration capacity of the electrochemical sensor, allowing to develop a simple, rapid and sensitive analysis in the detection of lead and cadmium in marine resources.