Corona discharge ion mobility spectrometry with orthogonal acceleration time of flight mass spectrometry for monitoring of volatile organic compounds

We demonstrate the application of corona discharge ion mobility spectrometry with orthogonal acceleration time of flight mass spectrometry (CD IMS-oaTOF) for volatile organic compounds (VOCs) monitoring. Two-dimensional (2D) IMS-oaTOF spectra of VOCs were recorded in nearly real time. The corona discharge atmospheric pressure chemical ionization (APCI) source was operated in positive mode in nitrogen and air. The CD ion source generates in air H(3)O(+)(H(2)O)(n) and NO(+). The NO(+) offers additional possibility for selective ionization and for an increase of the sensitivity of monoaromatic compounds. In addition to H(3)O(+)(H(2)O)(n) and NO(+), we have carried out ionization of VOCs using acetone as dopant gas ((CH(3))(2)COH(+)). Sixteen model VOCs (tetrahydrofuran, butanol, n-propanol, iso-propano, acetone, methanol, ethanol, toluene, benzene, amomnia, dioxan, triethylamine, acetonitrile, formaldehyde, m-xylene, 2,2,2-trifluoroethylamine) were tested using these ionization techniques.     

Negative chemical ionization GC/MS determination of nitrite and nitrate in seawater using exact matching double spike isotope dilution and derivatization with triethyloxonium tetrafluoroborate

The alkylation of nitrite and nitrate by triethyloxonium tetrafluoroborate allows determination of their ethyl esters by headspace gas chromatography/mass spectrometry (GC/MS). In the present study, significant improvement in analytical performance is achieved using negative chemical ionization providing detection limits of 150 ng/L for NO(2)(-) and 600 ng/L for NO(3)(-), an order of magnitude better than those achieved using electron impact ionization. The derivatization procedure was optimized and alkaline conditions adopted to minimize conversion of nitrite to nitrate (determined to be 0.07% at 100 mg/L NO(2)(-)) and to avoid the exchange of oxygen between the analytes and the solvent (water). Quantitation entails use of isotopically enriched standards (N(18)O(2)(-) and (15)NO(3)(-)), which also permits monitoring of potential conversion from nitrite to nitrate during the analysis (double spike isotope dilution).     

Development of a chemical ionization ion trap mass spectrometric method for trace level determination of molecular halogens

An ion trap mass spectrometric technique using negative ion chemical ionization has been developed for the quantitative determination of the molecular halogen species Br(2), Cl(2), and BrCl. The technique utilizes NO(2)(-) as a chemical ionization reagent in an electron-transfer reaction to form the corresponding molecular anions of the halogen species, lending excellent selectivity to the measurement. Reaction rate experiments performed in the ion trap yield a rate constant for Br(2) + NO(2)(-) --> Br(2)(-) + NO(2) of (1.4 +/- 0.6) x 10(-)(9) cm(3) molecule(-)(1) s(-)(1), determined relative to published data for Cl(2) + NO(2)(-) --> Cl(2)(-) + NO(2). This paper describes a mass spectrometer pinhole inlet design and cryogenic preconcentration system for detection of the molecular halogens at atmospherically relevant concentrations. Linear calibration curves were obtained for Cl(2) and Br(2) over 3 orders of magnitude and indicate limits of detection of 50 and 8 pmol for 3.8- and 5.1-L samples, respectively, corresponding to 220 and 50 parts per trillion (mole/mole). Quantitation is based on the total signal at m/z values of 70, 72, and 74 for Cl(2) and 158, 160, and 162 for Br(2). The effects of water vapor on the cryogenic preconcentration step are quantitatively assessed.     

Synthesis of a novel layered double hydroxides [MgAl(4)(OH)(12)](Cl)(2)·2.4H(2)O and its anion-exchange properties

A novel layered double hydroxide of Mg and Al with composition [Mg(0.96)Al(4.00)(OH)(12)]Cl(1.86)(CO(3))(0.03)·2.4H(2)O, designated as MgAl(4)-Cl, was synthesized by mixing crystalline gibbsite (γ-Al(OH)(3)) and solid MgCl(2)·6H(2)O with subsequent hydrothermal treatment at 160 °C for 72h. The MgAl(4)-Cl exhibited a crystalline material of a layered structure, as evidenced from X-ray diffraction. Anion uptake experiments with the MgAl(4)-Cl showed that Cl(-) in the interlayer space can be exchanged with anions such as Br(-), H(2)PO(4)(-), CO(3)(2-) or dodecyl sulfate (DS(-)) from aqueous solutions with preservation of the layered structure. Uptake of NO(3)(-), BrO(3)(-) or SO(4)(2-) on the MgAl(4)-Cl showed different behavior; these anions can be exchanged within 1h maintaining the layered structure, but a release of Mg(2+) cations from the sample was observed with increased reaction time, resulting in collapse of the layered structure and formation of the gibbsite phase, as determined from chemical analyses and X-ray diffraction.     

Atmospheric pressure laser-induced acoustic desorption chemical ionization mass spectrometry for analysis of saturated hydrocarbons

We present atmospheric pressure laser-induced acoustic desorption chemical ionization (AP/LIAD-CI) with O(2) carrier/reagent gas as a powerful new approach for the analysis of saturated hydrocarbon mixtures. Nonthermal sample vaporization with subsequent chemical ionization generates abundant ion signals for straight-chain, branched, and cycloalkanes with minimal or no fragmentation. [M - H](+) is the dominant species for straight-chain and branched alkanes. For cycloalkanes, M(+?) species dominate the mass spectrum at lower capillary temperature (<100 °C) and [M - H](+) at higher temperature (>200 °C). The mass spectrum for a straight-chain alkane mixture (C(21)-C(40)) shows comparable ionization efficiency for all components. AP/LIAD-CI produces molecular weight distributions similar to those for gel permeation chromatography for polyethylene polymers, Polywax 500 and Polywax 655. Coupling of the technique to Fourier transform ion cyclotron resonance mass spectrometry (FTICR MS) for the analysis of complex hydrocarbon mixtures provides unparalleled mass resolution and accuracy to facilitate unambiguous elemental composition assignments, e.g., 1754 peaks (rms error = 175 ppb) corresponding to a paraffin series (C(12)-C(49), double-bond equivalents, DBE = 0) and higher DBE series corresponding to cycloparaffins containing one to eight rings. Isoabundance-contoured plots of DBE versus carbon number highlight steranes (DBE = 4) of carbon number C(27)-C(30) and hopanes of C(29)-C(35) (DBE = 5), with sterane-to-hopane ratio in good agreement with field ionization (FI) mass spectrometry analysis, but performed at atmospheric pressure. The overall speciation of nonpolar, aliphatic hydrocarbon base oil species offers a promising diagnostic probe to characterize crude oil and its products.     

Elemental analysis of organic species with electron ionization high-resolution mass spectrometry

We present a new elemental analysis (EA) technique for organic species (CHNO) that allows fast on-line analysis (10 s) and reduces the required sample size to approximately 1 ng, approximately 6 orders of magnitude less than standard techniques. The composition of the analyzed samples is approximated by the average elemental composition of the ions from high-resolution electron ionization (EI) mass spectra. EA of organic species can be performed on organic/inorganic mixtures. Elemental ratios for the total organic mass, such as oxygen/carbon (O/C), hydrogen/carbon (H/C), and nitrogen/carbon (N/C), in addition to the organic mass to organic carbon ratio (OM/OC), can be determined. As deviations between the molecular and the ionic composition can appear due to chemical influences on the ion fragmentation processes, the method was evaluated and calibrated using spectra from 20 compounds from the NIST database and from 35 laboratory standards sampled with the high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS). The analysis of AMS (NIST) spectra indicates that quantification of O/C is possible with an error (average absolute value of the relative error) of 30% (17%) for individual species. Precision is much better than accuracy at +/-5% in the absence of air for AMS data. AMS OM/OC has an average error of 5%. Additional calibration is recommended for types of species very different from those analyzed here. EA was applied to organic mixtures and ambient aerosols (sampled at 20 s from aircraft). The technique is also applicable to other EI-HRMS measurements such as direct injection MS.     

Real-time detection and identification of aqueous chlorine transformation products using QTOF MS

A screening technique has been developed that allows the rapid, real-time detection and identification of major transformation products of organic contaminants during aqueous oxidation experiments. In this technique, a target contaminant is dissolved in buffered water and chlorinated by the addition of sodium hypochlorite to give a free chlorine residual of 3 mg/L. Solution from the reaction vessel is combined with methanol and pumped directly into the electrospray ionization source of a quadrupole time-of-flight mass spectrometer (QTOF MS). The real-time decay of the target contaminant and the formation/decay of transformation products are then monitored using the QTOF MS. Subsequently, accurate mass measurements with internal mass calibration (<5 ppm mass error) and product ion scans are employed to identify these transformation products. Unlike other techniques, it requires no liquid chromatography, derivatization, or quenching of residual chlorine, all of which can interfere with transformation product analysis. To validate the technique, aqueous chlorination experiments were performed on triclosan, a previously studied environmental contaminant. Earlier research showing that triclosan underwent chlorine addition to form mono- and dichlorinated transformation products was successfully reproduced, demonstrating the feasibility of the technique. In addition, the technique revealed the formation of a stable oxygen radical-containing transformation product resulting from the oxidation of either mono- or dichlorinated triclosan. This triclosan transformation product was determined to have an empirical formula of C12H4O3Cl4 with 3.9 ppm mass error. Furthermore, atorvastatin, a commonly prescribed medication and environmental contaminant, was subjected to aqueous chlorination and studied with the technique. Atorvastatin underwent hydroxylation to form two transformation products with the empirical formulas C33H34FN2O6 (1.8 ppm mass error) and C26H29O5NF (2.9 ppm mass error).     

Analysis of base oil fractions by ClMn(H2O)+ chemical ionization combined with laser-induced acoustic desorption/fourier transform ion cyclotron resonance mass spectrometry

Laser-induced acoustic desorption (LIAD), combined with chemical ionization with the ClMn(H(2)O)(+) ion, is demonstrated to facilitate the analysis of base oils by Fourier transform ion cyclotron resonance mass spectrometry. The LIAD/ClMn(H(2)O)(+) method produces only one product ion, [ClMn + M](+), for each component (M) in base oils, thus providing molecular weight (MW) information for the analytes. With the exception of one sample, no fragmentation was observed. The mass spectra indicate the presence of homologous series of ions differing in mass by multiples of 14 Da (i.e., CH(2)). All peaks in the spectra correspond to ions with even m/z values and hence are formed from hydrocarbons with no nitrogen atoms, in agreement with the compositional nature of base oils. The MW distributions measured for two groups of base oil samples cover the range 350-600 Da, which is in excellent agreement with the values determined by gas chromatography. Moreover, the hydrocarbon types (i.e., paraffin and cycloparaffins with different numbers of rings) present in each base oil sample can be determined based on the m/z values of the product ions. Finally, the results obtained by using LIAD/ClMn(H(2)O)(+) indicate that the efficiency of the technique (combined desorption and ionization efficiency) is similar for different hydrocarbon types and fairly uniform over a wide molecular weight range, thus allowing quantitative analysis of the base oils. Hence, the product ions' relative abundances were used to determine the percentage of each type of hydrocarbon in the base oil. In summary, three important parameters (MW distributions, hydrocarbon types, and their relative concentrations) can be obtained in a single experiment. This mass spectrometric technique therefore provides detailed molecular-level information for base oils, which cannot be obtained by other analytical methods.     

Development of ion drift-chemical ionization mass spectrometry

An ion drift-chemical ionization mass spectrometry (ID-CIMS) technique has been developed to detect and quantify trace gases, including volatile organic compounds and inorganic species. The trace species are chemically ionized into positive or negative product ions with a well-controlled ion-molecule reaction time. The ID-CIMS method allows for quantification of the trace gases without the necessity of performing calibrations with authentic standards for the trace gases. Demonstrations of the ability of ID-CIMS to accurately quantify isoprene and HNO3 in a laboratory setting are presented. The results illustrate that the ID-CIMS technique facilitates detection and quantification of organic and inorganic species in laboratory kinetic investigations and field measurements.     

Use of a clustering reaction to detect low levels of moisture in bulk oxygen using an atmospheric pressure ionization mass spectrometer

Atmospheric pressure ionization mass spectrometry (APIMS) is being routinely used to quantify trace impurities in bulk gases used in the manufacture of semiconductor devices. APIMS has been successfully applied for the quantification of ppt levels of O(2), H(2)O, CO(2), and CH(4) in Ar, N(2), and He. However, it has not been successfully used to quantify trace impurities in bulk O(2) due to the low ionization potential of O(2). APIMS relies on charge-transfer reaction between the ions of the bulk gas molecules and impurity molecules. Since all the relevant impurity molecules have ionization potentials higher than that of O(2), APIMS has not been used to analyze for impurities in O(2). We report here the detection of sub-ppb levels of H(2)O in O(2) by making use of the clustering reaction between O(2)(+) and H(2)O. The declustering region in an APIMS, which is normally used to break apart unwanted and interfering clusters, has to be carefully adjusted to keep intact the weakly bound cluster O(2)(+)·H(2)O. Our results indicate a statistical detection limit of less than 300 ppt for the detection of H(2)O in O(2).     

Development and characterization of an aerosol time-of-flight mass spectrometer with increased detection efficiency

This paper describes the development and characterization studies of a more efficient aerosol time-of-flight mass spectrometer (ATOFMS), showing results for the on-line detection and determination of the size and chemical composition of single fine (100-300 nm) and ultrafine (<100 nm) particles. An aerodynamic lens inlet was implemented, replacing the converging nozzle inlet used on conventional ATOFMS instruments. In addition, the light scattering region was modified to enhance the scattering signals for smaller particles. Polystyrene latex spheres (PSL) with aerodynamic diameters ranging from 95 to 290 nm were used to characterize the particle sizing efficiency (product of particle transmission efficiency and particle scattering efficiency), particle detection efficiency (product of particle sizing efficiency and particle hit rate), and particle beam profile and perform instrument calibration. At number concentrations of <20 particles/cm(3), the particle sizing efficiencies were determined to be approximately 0.5% for 95 nm and approximately 47% for 290-nm PSL particles, while the particle detection efficiencies were measured to be approximately 0.3% for 95 nm and 44% for 290-nm PSL particles. This represents a significant increase (i.e., at least 3 orders of magnitude) in detection efficiencies for smaller particles over the conventional ATOFMS. In addition, the beam profiles for PSL particles of various sizes were measured in the ion source of the mass spectrometer and follow a Gaussian distribution with a full width at half-maximum of approximately 0.35 mm. The resulting higher detection efficiencies allow ATOFMS to obtain higher temporal resolution measurements of the composition of fine and ultrafine individual particles as demonstrated in initial ambient measurements in La Jolla, CA. At typical ambient particle number concentrations of 10(2)-10(3) particles/cm(3), approximately 30 000 particles with aerodynamic diameters of <300 nm were detected with average 24-h hit rates of 30% for particles between 50 and 300 nm. This advancement, allowing for high temporal resolution measurements of the composition of smaller particles with higher efficiency, adds to a growing number of instruments that can chemically characterize individual fine and ultrafine particles, with the goal of providing new insights into a number of areas including environmental and material sciences, health effects studies, industrial hygiene, and national security.     

Electrospray Ion Chromatography-Tandem Mass Spectrometry of Bromate at Sub-ppb Levels in Water

An electrospray ion chromatography-tandem mass spectrometry (IC-MS/MS) method has been developed for the analysis of bromate ions in water. This IC-MS/MS method improves the limit of detection of bromate ions by a factor of 10. The method consists of solid phase extraction with an ion exchange column and elution of the analyte with water/methanol ammonium sulfate eluent on-line with a negative ion electrospray mass spectrometry detection. SPE requires sample pretreatment to remove any major ions that displace bromate, consisting of eliminating SO(4)(2)(-), Cl(-), and HCO(3)(-) ions respectively with barium-form, silver-form, and acid (H(+)-form) exchange resins. The methanolic sulfate eluent permits IC-MS coupling via an electrospray interface. BrO(3)(-) was selected in the first quadrupole (Q1) at two m/z values, 127 and 129, according to the isotope contributions of (79)Br and (81)Br. After fragmentation in the collision cell (second quadrupole, Q2), the third quadrupole (Q3) analyzes the product ions as (M - O)(-), (M - 2O)(-), and (M - 3O)(-). Among the six recordable transitions, four were selected, the other two yielding high background. A lowered resolution raised sensitivity by a factor of up to 3. The limit of quantitation of this method was 0.1 μg/L.     

Sensing of H2O2 at low surface density assemblies of Pt nanoparticles in polyelectrolyte

Amperometric detection of H2O2 was studied at random arrays of 2.5 nm polyacrylate-capped Pt nanoparticles (NP) assembled in poly(diallydimethylammonium chloride), PDDA, as a function of NP surface coverage. The arrays were assembled by varying the adsorption time of PDDA-modified electrodes in the nanoparticles solution. Pt NP-on-PDDA assemblies exhibited significant sensitivity and stability facing constant anodic polarization and a low limit of detection at small Pt mass in submonolayer coverage. The current output was measured at approximately 0.5 A M(-1) cm(-2)(geom) over a linear range from 42 nM to 0.16 mM H2O2 at a loading of 0.87 microg(Pt)/cm(2) or an estimated coverage of 0.4 of an assumed monolayer, or higher, and decreased with decreasing NP surface density to 0.2 A M(-1) cm(-2)(geom) at a Pt loading of 190 ng/cm. On the other hand, the intrinsic sensitivity measured relative to the real Pt surface area increased with decreasing coverage and reached a significant limiting value of 0.9 A M(-1) cm(-2) real at approximately 190-380 ng/cm(2). The behavior shows a significant effective turnover rate per Pt site and mass (1 A M(-1)/microg of Pt) in loosely packed assemblies, while overlap of individual diffusion fields (of particles or islands) and inaccessibility of some active sites lowers the sensitivity per nanoparticle in densely packed arrays. The reported trend agrees with the behavior of ultramicroelectrode arrays.     

Application of time-of-flight aerosol mass spectrometry for the online measurement of gaseous molecular iodine

Here we present a new application of a time-of-flight aerosol mass spectrometer (TOF-AMS) for the measurement of atmospheric trace gases in real-time. Usually, TOF-AMS instruments are not sensitive to gas-phase species due to the aerodynamic particle focusing inlet system which reduces the gas phase species by a factor of about 10(7) relative to the particle phase. This efficient removal of the gas phase and the resulting high relative enrichment of particles is one reason for the very high sensitivity of TOF-AMS instruments for particle phase compounds (detection limits in the sub-μg/m(3)-range for online measurements with 1 min integration time), which allows application of the instruments even under clean atmospheric conditions. Here we use artificially generated particles as sampling probes to transfer selected atmospheric trace gases into the particle phase before entering the AMS (gaseous compound trapping in artificially generated particles-AMS, GTRAP-AMS). The sampling probe particles are mixed with the gaseous analytes upstream of the TOF-AMS in a 0.5 L flow tube. As an exemplary application of the method, the measurement of trace levels of gaseous molecular iodine is demonstrated. α-Cyclodextrin (α-CD/NH(4)Br) particles are used as selective sampling probes to transfer molecular iodine into the AMS. A detection limit in the subparts-per-billion (sub-ppb) range was achieved. The method was compared to a recently developed off-line method that combines denuder sampling of gaseous I(2) and gas chromatography/mass spectrometry (GC/MS) analysis. To demonstrate the usability of the method, temporally resolved I(2) emission profiles from a brown algae species (Laminaria saccharina) under exposure of ambient ozone levels were investigated. Total I(2) release rates of 36.5 pmol min(-1) grams fresh weight (gFW)(-1) at 100 pbb O(3) and 33.4 pmol min(-1) gFW(-1) at 50 ppb O(3) were obtained within the first hour of ozone exposure.     

Prussian blue based nanoelectrode arrays for H(2)O(2) detection

We propose to form nanoelectrode arrays by deposition of the electrocatalyst through lyotropic liquid crystalline templates onto inert electrode support. Whereas Prussian Blue is known to be a superior electrocatalyst in hydrogen peroxide reduction, carbon materials used as electrode support demonstrate only a minor activity. We report on the possibility for nanostructuring of Prussian Blue by its electrochemical deposition through lyotropic liquid crystalline templates, which is noticed from atomic force microscopy images of the resulting surfaces. The resulting Prussian Blue based nanoelectrode arrays in flow injection analysis mode demonstrate a sub-part-per-billion detection limit (1 x 10(-)(8) M) and a linear calibration range starting exactly from the detection limit and extending over 6 orders of magnitude of H(2)O(2) concentrations (1 x 10(-)(8) to 1 x 10(-)(2) M), which are the most advantageous analytical performances in hydrogen peroxide electroanalysis.     

Low-temperature plasma ionization ion mobility spectrometry

In this research work, the capability of low-temperature plasma (LTP) as an ionization source for ion mobility spectrometry (IMS) has been investigated for the first time. This new ionization source enhances the potential of IMS as a portable analytical tool and allows direct analysis of various chemical compounds without having to evaporate the analyte or seek a solvent or reagent whatsoever. The effects of parameters such as the flow rate of the discharge gas, plasma voltage, and positioning of the LTP on the IMS signal were investigated. The positive reactant ions generated by the LTP ionization source were similar to those created in a corona discharge ionization source, where the proton clusters ((H(2)O)(n)H(+)) are the most abundant reactant ion, and in the negative mode, in addition to a saturated electron peak, several negative reactant ions (e.g., NO(x)(-)) were observed too. These reactant ions subsequently ionized the gaseous samples directly and liquids or solids after evaporation by plasma desorption. The ion mobility spectra of a few selected compounds, including explosives, drugs, and amines, were obtained to evaluate the new ionization source in positive and negative modes, and the reduced mobility values (K(0)) of the originated ions were calculated. Furthermore, the method has also been applied to obtain the figures of merit for acetaminophen as a test compound. The results obtained are promising enough to ensure the use of LTP as a desorption/ionization source in IMS for analytical applications.     

Isotope (18)O/(16)O Ratio Measurements of Water Vapor by use of Photoacoustic Spectroscopy

We applied a photoacoustic spectroscopy technique to isotope ratio measurements of (16)O and (18)O in water-vapor samples, using a pulsed tunable dye laser pumped by a Nd:YAG laser. The fourth overtone bands (4nu(OH)) of water molecules near 720 nm were investigated. We identified the absorption lines of H(2)(16)O and H(2)(18)O in the photoacoustic spectra that we measured by using an (18)O-enriched water sample and the HITRAN database. We measured the difference in the (18)O/(16)O isotope ratios for normal distilled water and Antarctic ice, using the photoacoustic method. The value obtained for the difference between the two samples is delta(18)O = -32 ? 16 per thousand, where the indicated deviation was a 1varsigma value among 240-s measurements, whereas the value measured with a conventional isotope mass spectrometer was delta(18)O = -28 ? 2 per thousand. This method is demonstrated to have the potential of a transportable system for in situ and quick measurements of the H(2)(18)O/H(2)(16)O ratio in the environment.     

Detection of pesticide residues on individual particles

An aerosol time-of-flight mass spectrometer (ATOFMS) is used to analyze the size and composition of individual particles containing pesticides. Pesticide residues are found in the atmosphere as a result of spray drift, volatilization, and suspension of coated soils. The ability of the ATOFMS to identify the presence of these contaminants on individual particles is assessed for particles created from pure solutions of several commonly used pesticides, as well as pesticides mixed with an organic matrix, and coated on soils. The common names of the pesticides studied are 2,4-D, atrazine, chlorpyrifos, malathion, permethrin, and propoxur. Analysis of the mass spectra produced by single- and two-step laser desorption/ionization of pesticide-containing particles allows for identification of peaks that can be used for detection of pesticide residues in the ambient aerosol. The identified marker peaks are used to approximate detection limits for the pesticides applied to soils, which are on the order of a fraction of a monolayer for individual particles. Results suggest that this technique may be useful for studying the real-time partitioning and distribution of pesticides in the atmosphere immediately following application in agricultural regions.     

Comparison of mass spectral techniques using organic peroxides related to artemisinin

The mass spectra of three peroxides related to artemisinin (1) are compared in nine different ionization modes. Ion trap mass spectrometry (MS/MS) spectra reveal numerous pathways for the electron impact (EI) decompositions. In the EI mode, the best spectra are obtained by using the ion trap mass spectrometer at low temperatures. Loss of oxygen is observed with the other EI spectrometers, suggesting catalytic decomposition in the ion source. Methane positive and negative chemical ionization (CI) spectra show considerable fragmentation, while isobutane CI spectra show only (M + H)+ for 1 and (M + H - H2O)+ for dihydroartemisinin (2) and (3). An unusually abundant (2M + H)+ is observed for 1 in both positive-ion plasma desorption and fast atom bombardment mass spectra.     

Quantification of nitryl chloride at part per trillion mixing ratios by thermal dissociation cavity ring-down spectroscopy

Nitryl chloride (ClNO(2)) is an important nocturnal nitrogen oxide reservoir species in the troposphere. Here, we report a novel method, thermal dissociation cavity ring-down spectroscopy (TD-CRDS), to quantify ClNO(2) mixing ratios with tens of parts-per-trillion by volume (pptv) sensitivity. The mixing ratios of ClNO(2) are determined by blue diode laser CRDS of NO(2), produced from quantitative thermal dissociation of ClNO(2) in an inlet heated to 450 °C, relative to NO(2) observed in an unheated reference channel. ClNO(2) was generated by passing Cl(2) gas over a slurry containing a 1:10 mixture of NaNO(2) and NaCl. The TD-CRDS response was evaluated using parallel measurements of ClNO(2) by chemical ionization mass spectrometry (CIMS) using I(-) as the reagent ion and NO(y) (= NO + NO(2) + HNO(3) + ΣRO(2)NO(2) + ΣRONO(2) + HONO + 2N(2)O(5) + ClNO(2) + ...) chemiluminescence (CL). The linear dynamic range extends from the detection limit of 20 pptv (1 σ, 1 min) to 30 parts-per-billion by volume (ppbv), the highest mixing ratio tested. The ClNO(2) TD profile overlaps with those of alkyl nitrates, which has implications for nocturnal measurements of total alkyl nitrate (ΣAN = ΣRONO(2)) abundances by thermal dissociation (with detection as NO(2)) in ambient air.