Reagent Ions Research Articles

Measurement of ammonia, amines and iodine compounds using protonated water cluster chemical ionization mass spectrometry

Abstract. Here we describe the design and performance of a new water cluster chemical ionization–atmospheric pressure interface time-of-flight mass spectrometer (CI-APi-TOF). The instrument selectively measures trace gases with high proton affinity such as ammonia and dimethylamine, which are important for atmospheric new particle formation and growth. Following the instrument description and characterization, we demonstrate successful measurements at the CERN CLOUD (Cosmics Leaving OUtdoor Droplets) chamber where very low ammonia background levels of ∼4 pptv were achieved (at 278 K and 80 % RH). The limit of detection of the water cluster CI-APi-TOF is estimated to be ∼0.5 pptv for ammonia. Although no direct calibration was performed for dimethylamine (DMA), we estimate its detection limit is at least 3 times lower. Due to the short ion–molecule reaction time and high reagent ion concentrations, ammonia mixing ratios up to at least 10 ppbv can be measured with the instrument without significant reagent ion depletion. Besides the possibility to measure compounds like ammonia and amines (dimethylamine), we demonstrate that the ionization scheme is also suitable for the measurement of trace gases containing iodine. During CLOUD experiments to investigate the formation of new particles from I2, many different iodine-containing species were identified with the water cluster CI-APi-TOF. The compounds included iodic acid and neutral molecular clusters containing up to four iodine atoms. However, the molecular structures of the iodine-containing clusters are ambiguous due to the presence of an unknown number of water molecules. The quantification of iodic acid (HIO3) mixing ratios is performed from an intercomparison with a nitrate CI-APi-TOF. Using this method the detection limit for HIO3 can be estimated as 0.007 pptv. In addition to presenting our measurements obtained at the CLOUD chamber, we discuss the applicability of the water cluster Ci-APi-TOF for atmospheric measurements.

Capability of CI-Orbitrap for Gas-Phase Analysis in Atmospheric Chemistry: A Comparison with the CI-APi-TOF Technique.

Chemical ionization Orbitrap mass spectrometry (CI-Orbitrap) represents a promising new technique for gas-phase analysis in analytical and atmospheric chemistry mainly due to its very high mass resolving power. In this work, we performed the first side-by-side comparison between a CI-Orbitrap and the widely used atmospheric pressure interface time-of-flight mass spectrometry (CI-APi-TOF) using two different chemical ionization methods, i.e., acetate-ion-based (CH3COO-) and aminium-ion-based (n-C3H7NH3+) schemes. The capability of the CI-Orbitrap at accurately measuring low concentrations of gaseous species formed from the oxidation of α-pinene was explored. Although this study reveals a lack of linearity of the CI-Orbitrap when measuring product ions at very low concentrations (<1 × 106 molecules cm-3), very good agreement between both techniques can be achieved by applying a newly developed linearity correction. It is experimentally shown that the correction function is independent of the reagent ion used. Thus, accurate quantification of organic compounds at concentrations as low as 1 × 105 molecules cm-3 by the CI-Orbitrap can be achieved. Finally, by means of tandem mass spectrometry, the unique capability of the Orbitrap allows the direct determination of the binding energy of cluster ions between analyte and reagent ions, that is needed for the assessment of a chosen ionization scheme.

The good, the bad and the aged: Predicting sensory quality of anhydrous milk fat by PTR/SRI-Tof-MS analysis and data mining

Due to its versatility, anhydrous milk fat (AMF) has become more popular as a food industry ingredient, but its quality control remains a critical challenge. A direct injection mass spectrometry technique was applied to predict sensory quality of AMF. Volatilome analysis through proton transfer reaction mass spectrometry (PTR-MS) was used to classify 39 industrial samples of AMF according to industrial sensory evaluation and to accelerated ageing. A selective reagent ion system was used to evaluate the suitability of PTR-MS alternative ionisation modes for quality control. Supervised multivariate data analysis successfully classified samples and showed that samples exposed to accelerated shelf life at 50 °C presented higher intensities of most volatiles, especially for the ones derived from oxidation like aldehydes and ketones, while samples with an acceptable quality level had lower emissions of volatiles. PTR-MS technique is ideal to support agroindustry sensory quality programs requiring rapid on-line analytical information.

Imaging VOC distribution in cities and tracing VOC emission sources with a novel mobile proton transfer reaction mass spectrometer

Volatile organic compounds (VOCs) are important precursors of ozone (O3) and secondary organic aerosols (SOAs). Tracing VOC pollution sources is important for controlling VOC emissions and reducing O3 and SOAs. We built a novel mobile proton transfer reaction mass spectrometry (M-PTR-MS) instrument to image the distribution of VOCs and trace their emission sources in cities and industrial parks. The M-PTR-MS is composed of a vibration-resistant proton transfer reaction mass spectrometry (PTR-MS) with a global positioning system receiver, modified box vehicle, and geographic information system (GIS) software. The PTR-MS, mounted on a vehicle, sends VOC data and vehicle position information to the GIS software. These data are used to image the space distribution of VOCs in real time while the vehicle platform is in motion and the VOC sources are precisely traced using the GIS. The spatial data resolution of the M-PTR-MS is typically 0.8 m. The limits of detection, sensitivity, and repeatability of the M-PTR-MS are 43.5 ppt, 347 counts ppb−1, and 2.4% (RSD, n = 5), respectively. The intensity of reagent ions is stable over 8 h (RSD = 0.45%). Compared with commercial PTR-MS equipment, the M-PTR-MS demonstrated high consistency, with a correlation coefficient of 92.665%. Several field experiments were conducted in China using the M-PTR-MS. In one field experiment, the VOC distribution along three different routes was surveyed; the navigation monitoring lasted 1.8 h over a distance of 26.7 km at an average speed of 15 km h−1. The VOC sources in an industrial park were identified by analyzing the components near different factories. The main species from a VOC source in an underground garage was related to paint. The M-PTR-MS instrument can be used by environmental protection agencies to trace VOC pollution sources in real time, and by researchers to survey VOC emissions in regions of concern.

Simultaneous detection of ozone and nitrogen dioxide by oxygen anion chemical ionization mass spectrometry: a fast-time-response sensor suitable for eddy covariance measurements

Abstract. We report on the development, characterization, and field deployment of a fast-time-response sensor for measuring ozone (O3) and nitrogen dioxide (NO2) concentrations utilizing chemical ionization time-of-flight mass spectrometry (CI-ToFMS) with oxygen anion (O2-) reagent ion chemistry. We demonstrate that the oxygen anion chemical ionization mass spectrometer (Ox-CIMS) is highly sensitive to both O3 (180 counts s−1 pptv−1) and NO2 (97 counts s−1 pptv−1), corresponding to detection limits (3σ, 1 s averages) of 13 and 9.9 pptv, respectively. In both cases, the detection threshold is limited by the magnitude and variability in the background determination. The short-term precision (1 s averages) is better than 0.3 % at 10 ppbv O3 and 4 % at 10 pptv NO2. We demonstrate that the sensitivity of the O3 measurement to fluctuations in ambient water vapor and carbon dioxide is negligible for typical conditions encountered in the troposphere. The application of the Ox-CIMS to the measurement of O3 vertical fluxes over the coastal ocean, via eddy covariance (EC), was tested during the summer of 2018 at Scripps Pier, La Jolla, CA. The observed mean ozone deposition velocity (vd(O3)) was 0.013 cm s−1 with a campaign ensemble limit of detection (LOD) of 0.0027 cm s−1 at the 95 % confidence level, from each 27 min sampling period LOD. The campaign mean and 1 standard deviation range of O3 mixing ratios was 41.2±10.1 ppbv. Several fast ozone titration events from local NO emissions were sampled where unit conversion of O3 to NO2 was observed, highlighting instrument utility as a total odd-oxygen (Ox=O3+NO2) sensor. The demonstrated precision, sensitivity, and time resolution of this instrument highlight its potential for direct measurements of O3 ocean–atmosphere and biosphere–atmosphere exchange from both stationary and mobile sampling platforms.

Selected ion flow tube mass spectrometry analyses of isobaric compounds methanol and hydrazine in humid air.

The volatile compounds generated by the electrochemical reduction of atmospheric carbon dioxide and nitrogen include isobaric methanol (CH3 OH) and, potentially, hydrazine (N2 H4 ). To achieve quantification of hydrazine molecules by selected ion flow tube mass spectrometry (SIFT-MS), its reactions with H3 O+ , NO+ and O2 + reagent ions must be understood. A SIFT study (using a SIFT-MS instrument) was carried out to obtain rate coefficients and product ions for the reactions of H3 O+ , NO+ and O2 + reagent ions with N2 H4 and CH3 OH molecules present in the humid headspace of their aqueous solutions. Using the kinetics data obtained, solution headspace concentrations were determined for both compounds as a function of their liquid-phase concentrations at 10, 20 and 35°C. Both compounds react with H3 O+ ions via rapid proton transfer to produce CH3 OH2 + and H5 N2 + ions with the common m/z value of 33. It is revealed that NO+ rapidly transfers charge to N2 H4 (rate coefficient k = 2.3 × 10-9 cm3 s-1 ) but only slowly associates with CH3 OH (k2eff = 7.1 × 10-11 cm3 s-1 ). Thus, selective analysis can be achieved using both H3 O+ and NO+ reagent ions. The headspace methanol vapour concentration was found to increase with increasing solution temperature, but that of hydrazine decreased with an associated increase of ammonia (NH3 ) as measured with O2 + reagent ions. The isobaric compounds methanol and hydrazine can be separately analysed in real time by SIFT-MS using H3 O+ and NO+ reagent ions, even when they co-occur in humid air. The evolution of hydrazine from aqueous solutions can be quantitatively monitored together with its decomposition at elevated temperatures.

Condensed Phase Membrane Introduction Mass Spectrometry with In Situ Liquid Reagent Chemical Ionization in a Liquid Electron Ionization Source (CP-MIMS-LEI/CI)

Direct mass spectrometry has grown significantly due to wide applicability, relative ease of use, and high sample throughput. However, many current direct mass spectrometry methods are largely based on ambient ionization techniques that can suffer from matrix effects and poor selectivity. A strategy that addresses these shortcomings is condensed phase membrane introduction mass spectrometry-liquid electron ionization utilizing in situ liquid reagent chemical ionization (CP-MIMS-LEI/CI). In CP-MIMS measurements, a semipermeable hollow fiber polydimethylsiloxane membrane probe is directly immersed into a complex sample. Neutral, hydrophobic analytes permeating the membrane are entrained by a continuously flowing liquid acceptor phase (nL/min) to an LEI/CI source, where the liquid is nebulized, followed by analyte vaporization and ionization. This study marks the first intentional exploitation of the liquid CP-MIMS acceptor phase as an in situ means of providing liquid chemical ionization (CI) reagents for improved analyte sensitivity and selectivity (CP-MIMS-LEI/CI). Acetonitrile and diethyl ether were used as a combination acceptor phase/CI proton transfer reagent system for the direct analysis of dialkyl phthalates. Using isotopically labeled reagents, the gas phase ionization mechanism was found to involve reagent autoprotonation, followed by proton transfer to dialkyl phthalates. A demonstration of the applicability of CP-MIMS-LEI/CI for rapid and sensitive screening of bis(2-ethylhexyl) phthalate in house dust samples is presented. The detection limit in house dust (6 mg/kg) is comparable to that obtained by conventional analyses, but without time-consuming sample workup or chromatographic separation steps.

Mass Spectrometric Characterization of the Partial Oxidation Process of a Gasoline Surrogate Induced by a Dielectric Barrier Discharge.

Plasma-assisted combustion can improve the thermal efficiency and stability of internal combustion engines; based on this, among various types of discharge method, surface dielectric barrier discharge (SDBD) induced partial oxidation of hydrocarbons was investigated in this study. To demonstrate the general mechanisms of SDBD-induced partial oxidation of gasoline, we used a five-component gasoline surrogate (S5R), which consisted of a mixture of alkanes (isooctane, n-heptane, and methylcyclohexane), alkenes (trimethyl pentene isomers), and toluene, as the model. The detailed process of SDBD-induced partial oxidation of hydrocarbon was investigated by Fourier transform infrared spectroscopy, ion attachment mass spectrometry, and density functional theory calculation. SDBD irradiation of the hydrocarbon/air mixture induced dissociation of oxygen molecule through direct electron impact and collision with excited nitrogen molecules, and the resultant oxygen atom then reacted with a hydrocarbon molecule. Alkane and toluene were converted to alkyl hydroperoxide by a reaction with the oxygen atom and subsequent attachment of O2. The resultant alkyl hydroperoxide then provided a ketone and/or aldehyde. In contrast, the alkenes underwent attachment of an oxygen atom and were either converted to fragments containing a carbonyl group or to etoposide. Regarding the analytical method, the partially oxidized products were selectively ionized from the hydrocarbon/air mixture when Na+ was used as the reagent ion for ion attachment mass spectrometry.

Novel ionization reagent for the measurement of gas-phase ammonia and amines using a stand-alone atmospheric pressure gas chromatography (APGC) source.

Contaminants present in ambient air or in sampling lines can interfere with the target analysis through overlapping peaks or causing a high background. This study presents a positive outcome from the unexpected presence of N-methyl-2-pyrrolidone, released from a PALL HEPA filter, in the analysis of atmospherically relevant gas-phase amines using chemical ionization mass spectrometry. Gas-phase measurements were performed using a triple quadrupole mass spectrometer equipped with a modified atmospheric pressure gas chromatography (APGC) source which allows sampling of the headspace above pure amine standards. Gas-phase N-methyl-2-pyrrolidone (NMP) emitted from a PALL HEPA filter located in the inlet stream served as the ionizing agent. This study demonstrates that some alkylamines efficiently form a [NMP + amine+H]+ cluster with NMP upon chemical ionization at atmospheric pressure. The extent of cluster formation depends largely on the proton affinity of the amine compared with that of NMP. Aromatic amines (aniline, pyridine) and diamines (putrescine) were shown not to form cluster ions with NMP. The use of NMP as an ionizing agent with stand-alone APGC provided high sensitivity for ammonia and the smaller amines. The main advantages, in addition to sensitivity, are direct sampling into the APGC source and avoiding uptake on sampling lines which can be a significant problem with ammonia and amines.

Volatile compounds released by Nalophan; implications for selected ion flow tube mass spectrometry and other chemical ionisation mass spectrometry analytical methods.

Three analytical techniques were used to analyse the VOCs released into the nitrogen used to expand Nalophan bags, viz. gas chromatography/mass spectrometry (GC/MS), secondary electrospray ionization mass spectrometry (SESI-MS) and selected ion flow tube mass spectrometry (SIFT-MS). The most significant VOCs were identified and quantified by SIFT-MS as a function of storage time, temperature and humidity. The consistent results obtained by these three analytical methods identify 1,2-ethanediol (ethylene glycol) and 2-methyl-1,3-dioxolane as the major VOCs released by the Nalophan. Their concentrations are enhanced by increasing the bag storage temperature and time, reaching 170 parts-per-billion by volume (ppbv) for ethylene glycol and 34 ppbv for 2-methyl-1,3-dioxolane in humid nitrogen (absolute humidity of 5%) contained in an 8-L Nalophan bag stored at 37°C for 160 min. Using H3 O+ reagent ions for SIFT-MS and SESI-MS analyses, the following analyte ions (m/z values) are affected by the Nalophan impurities: 45, 63, 81, 89 and 99, which can compromise analyses of acetaldehyde, ethylene glycol, monoterpenes, acetoin, butyric acid, hexanal and heptane.

Interpretation of Ionization Mechanism Responsible for Reagent Ion and Analyte Formation in Microwave-Induced Plasma Desorption Ionization Mass Spectrometry.

Ambient desorption/ionization (ADI) sources coupled to mass spectrometer have gained increasing interest in the field of analytical chemistry for its fast and direct analysis of samples. Among many ADI sources, plasma-based ADI sources are an important branch. Despite its extensive use in mass spectrometry analysis, the ionization mechanism of these sources still remain uncertain. The study on ionization mechanism is of great significance to optimize the design of ion sources and to improve ionization efficiency. In this study, targeted research on a better understanding of afterglow distance effects on ionization process was conducted. Based on the quantified signal expression of reagent ions in mass spectrum, the concept that optimal atmospheric analysis distance of plasma ADI source is defined for the first time. From the perspective of mutual restriction effect between atmospheric components, the formation progress of reagent ions was visually revealed in detail, which involved the initial step of forming precursor reagent ions, the clusters reaction for increasing production of reagent ions, and the matrix effect results in reagent ion depletion. The formation mechanism of reagent ions further clarified the explicit reason for abundant reagent ions generated at an optimal distance. Most importantly, the analyte analysis results verified the significant impact of appropriate distance on ionization efficiency in afterglow region. It was confirmed that the quantity and type of reagent ions intimately influenced the status of analyte ions in mass spectrum.

Multi-scheme chemical ionization inlet (MION) for fast switching of reagent ion chemistry in atmospheric pressure chemical ionization mass spectrometry (CIMS) applications

Abstract. A novel chemical ionization inlet named the Multi-scheme chemical IONization inlet (MION), Karsa Ltd., Helsinki, Finland) capable of fast switching between multiple reagent ion schemes is presented, and its performance is demonstrated by measuring several known oxidation products from much-studied cyclohexene and α-pinene ozonolysis systems by applying consecutive bromide (Br−) and nitrate (NO3-) chemical ionization. Experiments were performed in flow tube reactors under atmospheric pressure and room temperature (22 ∘C) utilizing an atmospheric pressure interface time-of-flight mass spectrometer (APi-ToF-MS, Tofwerk Ltd., Thun, Switzerland) as the detector. The application of complementary ion modes in probing the same steady-state reaction mixture enabled a far more complete picture of the detailed autoxidation process; the HO2 radical and the least-oxidized reaction products were retrieved with Br− ionization, whereas the highest-oxidized reaction products were detected in the NO3- mode, directly providing information on the first steps and on the ultimate endpoint of oxidation, respectively. While chemical ionization inlets with multiple reagent ion capabilities have been reported previously, an application in which the charging of the sample occurs at atmospheric pressure with practically no sample pretreatment, and with the potential to switch the reagent ion scheme within a second timescale, has not been introduced previously. Also, the ability of bromide ionization to detect highly oxygenated organic molecules (HOM) from atmospheric autoxidation reactions has not been demonstrated prior to this investigation.

The H3O+(H2O)n Reagent Ion: Calculations of the Structure, Thermodynamic Parameters of Hydration, Equilibrium Composition, and Mobility

The H3O+(H2O)n reagent ion is widely used in ion mobility spectrometry and atmospheric pressure chemical ionization mass spectrometry. In this work, calculated data on the structure and properties of the H3O+(H2O)n (n = 0–4) reagent ion are obtained. They are of interest for the study of the regularities of chemical ionization and the prediction and interpretation of ion mobility spectra and mass spectra. Using quantum chemical methods, we calculated the structures and refined the isomeric composition of the H3O+(H2O)n ions. It was found that ions with n = 2, 3, and 4 have 2, 5, and 15 isomers, respectively. The most stable isomers, which possess branched non-cyclic structures with the H3O+ core, were determined. The thermodynamic parameters of hydration reactions of the most stable isomers of H3O+(H2O)n (n = 0–3) ions and the equilibrium composition of the reagent ion in a wide range of temperatures and concentrations of water vapor are computed. The obtained results agree with the available experimental and calculated data. Using the computed structural data and data on the composition of the reagent ion, its mobility was calculated by the trajectory method. The error of calculations is close to the experimental one.

Styrene radical cations for chemical ionization mass spectrometry analyses of monoterpene hydrocarbons.

Monoterpene hydrocarbons play an important role in the formation of secondary aerosol particles and in atmospheric chemistry. Thus, there is a demand to measure their individual concentrations in situ in real time. Currently, only the total concentration of monoterpenes C10 H16 can be determined by chemical ionization mass spectrometry techniques using reagent ions H3 O+ , NO+ and (C6 H6 )n +• without gas chromatographic separation. The styrene cation C8 H8 +• was investigated as a reagent for chemical ionization of monoterpenes. The modified selected ion flow drift tube, SIFDT, technique was used to characterize the differences in product ion distributions between α-phellandrene, α-pinene, γ-terpinene, β-pinene, ocimene, sabinene, 3-carene, (R)-limonene, camphene and myrcene. The monoterpene molecular cation C10 H16 +• is the main product (about 90%) for all isomers except (R)-limonene and camphene with an efficient channel of C8 H8 +• C10 H16 adduct formation and γ-terpinene with unexpectedly significant product ions at m/z 134 and 135 corresponding to losses of H2 and H. Utilization of the styrene cation for the ionization of monoterpenes is beneficial due to the very low fragmentation of the product ions. Specific association product ions for camphene and (R)-limonene and fragment product ions for γ-terpinene allow them to be distinguished from other isomers that produce mostly the molecular cation.

Real-time differentiation of ethylbenzene and the xylenes using selected ion flow tube mass spectrometry.

Monitoring of isomeric analytes using mass spectrometry usually requires a time-consuming chromatographic separation of the analytes before analysis. Selected ion flow tube mass spectrometry (SIFT-MS) can provide rapid direct analysis of ethylbenzene and xylene by utilizing the different reaction chemistry of the isomers. O2 + yields the same product ions from each isomer but in different ratios. OH- yields different product ions. The reaction chemistry of C8 H10 with the reagent ion OH- generated from a microwave discharge of moist air in a commercial SIFT-MS instrument was utilized in this study. The product ion from OH- yielded ions at different masses for each isomer. To gain an understanding of how the product ion from ethylbenzene of HO2 - was generated, a theoretical study of the potential reaction surface was undertaken that accounted for the experimental observations. Measurements of OH- with ethylbenzene showed the product ion to be HO2 - at m/z 33. The reaction of OH- with xylene yielded the major product ion at m/z 105, C8 H9 - . HO2 - also underwent a slow secondary reaction with CO2 and O2 present from air in the samples. These findings were supported by calculations of the potential energy surface for the reactions. Measurements made on a certified gas mixture of ethylbenzene and xylene in the concentration range up to 5000 ppbv gave a linear response for each analyte. A fast, efficient method was developed for monitoring xylene and ethylbenzene in a mixture without the need for chromatographic separation before analysis using SIFT-MS.

A novel method for producing NH4+ reagent ions in the hollow cathode glow discharge ion source of PTR-MS instruments

Proton-transfer-reaction mass spectrometry (PTR-MS) is seeing an increased use of NH4+ ions for the detection of amines and labile oxygenated organic compounds. NH4+ ions are usually generated from ammonia or ammonium-containing chemicals. We herein present a simple method for generating NH4+ reagent ions in the hollow cathode glow discharge ion source that nowadays most proton-transfer-reaction mass spectrometry (PTR-MS) instruments are equipped with. We show that NH4+ ions can be generated in high purity and yield by simply introducing a mixture of water vapor and nitrogen in the ion source. We also show that rapid switching (∼10 s loss of data) between the H3O+ and NH4+ operation modes is possible. Our new method can be easily implemented in most PTR-MS instruments that are currently in use, thus opening the possibility to easily operate the PTR-MS analyzer in the NH4+ chemical ionization mode.

Recent Developments in Gas-Phase Ion/Ion Reactions for Analytical Mass Spectrometry.

While the study of reactions between oppositely-charged ions has a long history, particularly within the context of plasmas and interstellar chemistry, the exploitation of such reactions for analytical applications was made possible with the advent of electrospray ionization (ESI). , ESI provides a means for generating abundant multiply-charged ions from a wide variety of molecular classes. It was then possible to use ESI to generate multiply-charged analyte or reagent ions for reactions with ions of opposite polarities without resulting in complete neutralization. The first description of ion/ion reaction studies using ESI was given by Loo et al. using a Y-tube reactor leading to the inlet of an atmosphere/vacuum interface coupled with a quadrupole mass filter. , This was an early example of ion/ion chemistry being effected prior to sampling ions into a mass spectrometer. The first implementation of ion/ion reactions within the context of a MSn experiment was demonstrated at Oak Ridge National Lab. , Thi...

Addition of fast gas chromatography to selected ion flow tube mass spectrometry for analysis of individual monoterpenes in mixtures

Abstract. Soft chemical ionization mass spectrometry (SCI-MS) techniques can be used to accurately quantify volatile organic compounds (VOCs) in air in real time; however, differentiation of isomers still represents a challenge. A suitable pre-separation technique is thus needed, ideally capable of analyses over a few tens of seconds. To this end, a bespoke fast gas chromatography (GC) instrument with an electrically heated 5 m long metallic capillary column was coupled to selected ion flow tube mass spectrometry (SIFT-MS) measurements. To assess the performance of this combination, a case study of monoterpene isomer (C10H16) analyses was carried out. The monoterpenes were quantified by SIFT-MS using H3O+ reagent ions (analyte ions C10H17+, m∕z 137, and C6H9+, m∕z 81) and NO+ reagent ions (analyte ions C10H16+, m∕z 136, and C7H9+, m∕z 93). The combinations of the fragment ion relative intensities obtained using H3O+ and NO+ were shown to be characteristic of the individual monoterpenes. Two non-polar GC columns (Restek Inc.) were tested: the advantage of MXT-1 was shorter retention, whilst the advantage of MXT-Volatiles was better separation. Thus, it is possible to identify components of a monoterpene mixture in less than 45 s using the MXT-1 column and to separate them in less than 180 s using the MXT-Volatiles column. Quality of the separation and the sensitivity of present technique (limit of detection, LOD, ∼16 ppbv) was found to be inferior compared to commercially available fast GC solutions coupled with proton transfer reaction mass spectrometry (PTR-MS, LOD ∼1 ppbv) due to the limited sample flow through the column. However, using combinations of two reagent ions improved identification of monoterpenes not well resolved by the chromatograms. As an illustrative example, the headspace of needle samples of three conifer species was analysed by both reagent ions and with both columns showing that mainly α-pinene, β-pinene and 3-carene were present. The system can thus be used for direct rapid monitoring of monoterpenes above 20 ppbv, such as applications in laboratory studies of monoterpene standards and leaf headspace analysis. Limitation of the sensitivity due to the total sample flow can be improved using a multi-column pre-separation.

Selective Reagent Ion Mass Spectrometric Investigations of the Nitroanilines

This paper presents an investigation of proton and charge transfer reactions to 2-, 3- and 4-nitroanilines (C6H6N2O2) involving the reagent ions H3O+·(H2O)n (n = 0, 1 and 2) and O2+, respectively, as a function of reduced electric field (60–240 Td), using Selective Reagent Ion–Time-of-Flight–Mass Spectrometry (SRI–ToF–MS). To aid in the interpretation of the H3O+·(H2O)n experimental data, the proton affinities and gas-phase basicities for the three nitroaniline isomers have been determined using density functional theory. These calculations show that proton transfer from both the H3O+ and H3O+·H2O reagent ions to the nitroanilines will be exoergic and hence efficient, with the reactions proceeding at the collisional rate. For proton transfer from H3O+ to the NO2 sites, the exoergicities are 171 kJ mol−1 (1.8 eV), 147 kJ mol−1 (1.5 eV) and 194 kJ mol−1 (2.0 eV) for 2-, 3- and 4-nitroanilines, respectively. Electron transfer from all three of the nitroanilines is also significantly exothermic by approximately 4 eV. Although a substantial transfer of energy occurs during the ion/molecule reactions, the processes are found to predominantly proceed via non-dissociative pathways over a large reduced electric field range. Only at relatively high reduced electric fields (> 180 Td) is dissociative proton and charge transfer observed. Differences in fragment product ions and their intensities provide a means to distinguish the isomers, with proton transfer distinguishing 2-nitroaniline (2–NA) from 3- and 4-NA, and charge transfer distinguishing 4-NA from 2- and 3-NA, thereby providing a means to enhance selectivity using SRI–ToF–MS.

Decomposition of flotation reagents in solutions containing metal ions. Part III: Comparison between xanthates and dithiocarbamates

With an increasing concern on environment and health, the issue of decomposition of various mining reagents which generates harmful impacts need to be timely handled. DTC (Dithiocarbamate), which play a similar role as xanthate in flotation as collector, was under investigation in this study using the systematic method developed for xanthate (Part I) to understand the effects of metal ions on the decomposition.It was found that DTC and xanthate have similarities with respect to decomposition: Cu2+ suppresses while Fe3+ promotes its decomposition; with an increase in the alkyl chain length, decomposition becomes weaker. With the same alkyl chain length, DTC decomposes less than xanthate. These observations can be explained by the molecular structures of the reagent anion and the derivatives such as dimer and metal complex (similar to xanthate, DTC forms cuprous or ferric DTC and di-DTC when interacting with Cu2+ or Fe3+). The longer the alkyl chain, the stronger the -CS2 moiety attaches to the R2N- in DTC or the RO- in xanthate, so the lower the decomposition of xanthate or DTC is. The -CS2 moiety attaches to the R2N- in DTC stronger than that to the RO- in xanthate, making xanthate decompose more than DTC. A proposed order of easiness for the -CS2 moiety to break up from xanthate or DTC is: cuprous complex < dimer < reagent anion < ferric complex by comparing molecular structures of the compounds formed by the reagent and metal ions. Thus, Cu2+ suppresses while Fe3+ promotes the decomposition. Investigation of the binding energy to break the -CS2 moiety from the molecules is necessary for future studies.