NIST Standards for Measurement, Instrument Calibration, and Quantification of Gaseous Atmospheric Compounds.

There are many gas phase compounds present in the atmosphere that affect and influence the earth's climate. These compounds absorb and emit radiation, a process which is the fundamental cause of the greenhouse effect. The major greenhouse gases in the earth's atmosphere are carbon dioxide, methane, nitrous oxide, and ozone. Some halocarbons are also strong greenhouse gases and are linked to stratospheric ozone depletion. Hydrocarbons and monoterpenes are precursors and contributors to atmospheric photochemical processes, which lead to the formation of particulates and secondary photo-oxidants such as ozone, leading to photochemical smog. Reactive gases such as nitric oxide and sulfur dioxide are also compounds found in the atmosphere and generally lead to the formation of other oxides. These compounds can be oxidized in the air to acidic and corrosive gases and contribute to photochemical smog. Measurements of these compounds in the atmosphere have been ongoing for decades to track growth rates and assist in curbing emissions of these compounds into the atmosphere. To accurately establish mole fraction trends and assess the role of these gas phase compounds in atmospheric chemistry, it is essential to have good calibration standards. The National Institute of Standards and Technology has been developing standards of many of these compounds for over 40 years. This paper discusses the development of these standards.

Issues with analyzing noble gases using gas chromatography with thermal conductivity detection.

The noble gases, namely neon, argon, krypton and xenon, have many uses including in incandescent and gas discharge lighting, in plasma televisions, shielding gas in welding, in lasers for surgery and semiconductors, and in magnetic resonance imaging (MRI) of the lungs. When incorporating these noble gases in industries, especially the medical field, it is important to know accurately the composition of the noble gas mixture. Therefore, there is a need for accurate gas standards that can be used to determine the noble gas amount-of-substance fraction in the appropriate mixture application. A recent comparison of mixtures containing four noble gases in a helium balance showed mixed results among National Metrology Institutes. Significant differences, 0.7 to 3.8% relative, were seen in the analytical amount-of-substance assignments versus the gravimetric value of the noble gases in the comparison mixture when using "binary standards", i.e. neon in helium, argon in helium and krypton in helium, as applied by the National Institute of Standards and Technology. Post-comparison studies showed that when all four noble gases were included in the standards, the agreement between analytical and gravimetric values was within 0.05% relative. Further research revealed that different carrier gases (hydrogen, helium and nitrogen) resulted in varying differences between the analytical and gravimetric values assignments. This paper will discuss the findings of these analytical comparisons. Graphical abstract ᅟ.

Development of a Northern Continental Air Standard Reference Material.

The National Institute of Standards and Technology (NIST) recently began to develop standard mixtures of greenhouse gases as part of a broad program mandated by the 2009 United States Congress to support research in climate change. To this end, NIST developed suites of gravimetrically assigned primary standard mixtures (PSMs) comprising carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) in a dry-natural air balance at ambient mole fraction levels. In parallel, the National Oceanic and Atmospheric Administration (NOAA) in Boulder, Colorado, charged 30 aluminum gas cylinders with northern hemisphere air at Niwot Ridge, Colorado. These mixtures, which constitute NIST Standard Reference Material (SRM) 1720 Northern Continental Air, were certified by NIST for ambient mole fractions of CO2, CH4, and N2O relative to NIST PSMs. NOAA-assigned values are also provided as information in support of the World Meteorological Organization (WMO) Global Atmosphere Watch (GAW) Program for CO2, CH4, and N2O, since NOAA serves as the WMO Central Calibration Laboratory (CCL) for CO2, CH4, and N2O. Relative expanded uncertainties at the 95% confidence interval are <±0.06% of the certified values for CO2 and N2O and <0.2% for CH4, which represents the smallest relative uncertainties specified to date for a gaseous SRM produced by NIST. Agreement between the NOAA (WMO/GAW) and NIST values based on their respective calibration standards suites is within 0.05%, 0.13%, and 0.06% for CO2, CH4, and N2O, respectively. This collaborative development effort also represents the first of its kind for a gaseous SRM developed by NIST.

Development of a southern oceanic air standard reference material.

In 2009, the United States Congress charged the National Institute of Standards and Technology (NIST) with supporting climate change research. As part of this effort, the Gas Sensing Metrology Group at NIST began developing new gas standard mixtures for greenhouse gas mixtures relevant to atmospheric measurements. Suites of gravimetrically prepared primary standard mixtures (PSMs) were prepared at ambient concentration levels for carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) in a dry-air balance. In parallel, 30 gas cylinders were filled, by the National Institute of Water and Atmospheric Research (NIWA) in Wellington, New Zealand, to high pressure from pristine southern oceanic air at Baring Head, New Zealand, and shipped to NIST. Using spectroscopic instrumentation, NIST analyzed the 30 cylinder samples for mole fractions of CO2, CH4, and N2O. Certified values were assigned to these mixtures by calibrating the instrumentation with the PSM suites that were recently developed at NIST. These mixtures became NIST Standard Reference Material (SRM) 1721 Southern Oceanic Air and are certified for ambient mole fraction, the first of their kind for NIST. The relative expanded uncertainties corresponding to coverage intervals with 95% probability are no larger than 0.06% of the certified values, representing the smallest uncertainties to date ever assigned to an NIST gas SRM.

Investigating adsorption/desorption of carbon dioxide in aluminum compressed gas cylinders.

Between June 2010 and June 2011, the National Institute of Standards and Technology (NIST) gravimetrically prepared a suite of 20 carbon dioxide (CO2) in air primary standard mixtures (PSMs). Ambient mole fraction levels were obtained through six levels of dilution beginning with pure (99.999%) CO2. The sixth level covered the ambient range from 355 to 404 µmol/mol. This level will be used to certify cylinder mixtures of compressed dry whole air from both the northern and southern hemispheres as NIST standard reference materials (SRMs). The first five levels of PSMs were verified against existing PSMs in a balance of air or nitrogen with excellent agreement observed (the average percent difference between the calculated and analyzed values was 0.002%). After the preparation of a new suite of PSMs at ambient level, they were compared to an existing suite of PSMs. It was observed that the analyzed concentration of the new PSMs was less than the calculated gravimetric concentration by as much as 0.3% relative. The existing PSMs had been used in a Consultative Committee for Amount of Substance-Metrology in Chemistry Key Comparison (K-52) in which there was excellent agreement (the NIST-analyzed value was -0.09% different from the calculated value, while the average of the difference for all 18 participants was -0.10%) with those of other National Metrology Institutes and World Meteorological Organization designated laboratories. In order to determine the magnitude of these losses at the ambient level, a series of "daughter/mother" tests were initiated and conducted in which the gas mixture containing CO2 from a "mother" cylinder was transferred into an evacuated "daughter" cylinder. These cylinder pairs were then compared using cavity ring-down spectroscopy under high reproducibility conditions (the average percent relative standard deviation of sample response was 0.02). A ratio of the daughter instrument response to the mother response was calculated, with the resultant deviation from unity being a measure of the CO2 loss or gain. Cylinders from three specialty gas vendors were tested to find the appropriate cylinder in which to prepare the new PSMs. All cylinders tested showed a loss of CO2, presumably to the walls of the cylinder. The vendor cylinders exhibiting the least loss of CO2 were then purchased to be used to gravimetrically prepare the PSMs, adjusting the calculated mole fraction for the loss bias and an uncertainty calculated from this work.

Methane standards made in whole and synthetic air compared by cavity ring down spectroscopy and gas chromatography with flame ionization detection for atmospheric monitoring applications.

There is evidence that the use of whole air versus synthetic air can bias measurement results when analyzing atmospheric samples for methane (CH4) and carbon dioxide (CO2). Gas chromatography with flame ionization detection (GC-FID) and wavelength scanned-cavity ring down spectroscopy (WS-CRDS) were used to compare CH4 standards produced with whole air or synthetic air as the matrix over the mole fraction range of 1600-2100 nmol mol(-1). GC-FID measurements were performed by including ratios to a stable control cylinder, obtaining a typical relative standard measurement uncertainty of 0.025%. CRDS measurements were performed using the same protocol and also with no interruption for a limited time period without use of a control cylinder, obtaining relative standard uncertainties of 0.031% and 0.015%, respectively. This measurement procedure was subsequently used for an international comparison, in which three pairs of whole air standards were compared with five pairs of synthetic air standards (two each from eight different laboratories). The variation from the reference value for the whole air standards was determined to be 2.07 nmol mol(-1) (average standard deviation) and that of synthetic air standards was 1.37 nmol mol(-1) (average standard deviation). All but one standard agreed with the reference value within the stated uncertainty. No significant difference in performance was observed between standards made from synthetic air or whole air, and the accuracy of both types of standards was limited only by the ability to measure trace CH4 levels in the matrix gases used to produce the standards.

Development and verification of air balance gas primary standards for the measurement of nitrous oxide at atmospheric levels.

The Gas Metrology Group at the National Institute of Standards and Technology (NIST) became active in developing primary standards at ambient levels of N2O in the 1980s, and this has continued through to the present. In recent years, interest in NIST-traceable standards has increased-not only at the ambient level of approximately 325 nmol mol(-1) (ppb) but at micromole per mole (ppm) levels as well. In order to support two in-process dry whole air standard reference materials (SRMs 1720 and 1721) and the NIST Traceable Reference Materials (NTRM) program, a project was implemented in the Gas Metrology Group to produce a complete suite of new primary standard materials (PSMs) of N2O with synthetic air (O2/N2) as the balance gas. Six levels of dilution, approximately 1 order of magnitude apart, were gravimetrically prepared and verified. Each level serves as the "parent mix" for the next level. This discussion describes the process of producing each level and then verifying its amount-of-substance fraction. Expanded uncertainties, k = 2, of 0.025% relative to the gravimetric amount-of-substance fraction were obtained at the ambient level. One standard from the final group of standards at the ambient amount-of-substance fraction level was compared with standards from the National Oceanographic and Atmospheric Administration and the Scripps Institution of Oceanography, two organizations experienced in gas standards preparation and ambient whole air measurements, and shows agreement to 0.07 nmol mol(-1) (0.02% relative) and 0.20 nmol mol(-1) (0.06% relative), respectively.

Preparation and validation of fully synthetic standard gas mixtures with atmospheric isotopic composition for global CO2 and CH4 monitoring.

We report the preparation and validation of the first fully synthetic gaseous reference standards of CO2 and CH4 in a whole air matrix with an isotopic distribution matching that is in the ambient atmosphere. The mixtures are accurately representative of the ambient atmosphere and were prepared gravimetrically. The isotopic distribution of the CO2 was matched to the abundance in the ambient atmosphere by blending (12)C-enriched CO2 with (13)C-enriched CO2 in order to avoid measurement biases introduced by measurement instrumentation detecting only certain isotopologues. The reference standards developed here have been compared with standards developed by the National Institute of Standards and Technology and standards from the WMO scale. They demonstrate excellent comparability.

International comparison of a hydrocarbon gas standard at the picomol per mol level.

Studies of climate change increasingly recognize the diverse influences of hydrocarbons in the atmosphere, including roles in particulates and ozone formation. Measurements of key nonmethane hydrocarbons (NMHCs) suggest atmospheric mole fractions ranging from low picomoles per mol (ppt) to nanomoles per mol (ppb), depending on location and compound. To accurately establish mole fraction trends and to relate measurement records from many laboratories and researchers, it is essential to have accurate, stable, calibration standards. In February of 2008, the National Institute of Standards and Technology (NIST) developed and reported on picomoles per mol standards containing 18 nonmethane hydrocarbon compounds covering the mole fraction range of 60 picomoles per mol to 230 picomoles per mol. The stability of these gas mixtures was only characterized over a short time period (2 to 3 months). NIST recently prepared a suite of primary standard gas mixtures by gravimetric dilution to ascertain the stability of the 2008 picomoles per mol NMHC standards suite. The data from this recent chromatographic intercomparison of the 2008 to the 2011 suites confirm a much longer stability of almost 5 years for 15 of the 18 hydrocarbons; the double-bonded alkenes of propene, isobutene, and 1-pentene showed instability, in line with previous publications. The agreement between the gravimetric values from preparation and the analytical mole fractions determined from regression illustrate the internal consistency of the suite within ±2 pmol/mol. However, results for several of the compounds reflect stability problems for the three double-bonded hydrocarbons. An international intercomparison on one of the 2008 standards has also been completed. Participants included National Metrology Institutes, United States government laboratories, and academic laboratories. In general, results for this intercomparison agree to within about ±5% with the gravimetric mole fractions of the hydrocarbons.

Stability assessment of gas mixtures containing monoterpenes in varying cylinder materials and treatments.

Studies of climate change increasingly recognize the diverse influences exerted by monoterpenes in the atmosphere, including roles in particulates, ozone formation, and oxidizing potential. Measurements of key monoterpenes suggest atmospheric mole fractions ranging from low pmol/mol (parts-per-trillion; ppt) to nmol/mol (parts-per-billion; ppb), depending on location and compound. To accurately establish the mole fraction trends, assess the role of monoterpenes in atmospheric chemistry, and relate measurement records from many laboratories and researchers, it is essential to have good calibration standards. The feasibility of preparing well-characterized, stable gas cylinder standards for monoterpenes at the nmol/mol level was previously tested using treated (Aculife IV) aluminum gas cylinders at NIST. Results for 4 of the 11 monoterpenes, monitored versus an internal standard of benzene, indicated stability in these treated aluminum gas cylinders for over 6 months and projected long-term (years) stability. However, the mole fraction of the key monoterpene ß-pinene decreased, while the mole fractions of α-pinene, d-limonene (R-(+)-limonene), p-cymene, and camphene (a terpene not present in the initial gas mixture) increased, indicating a chemical transformation of ß-pinene to these species. A similar pattern of decreasing mole fraction was observed in α-pinene where growth of d-limonene, p-cymene, and camphene has been observed in treated gas cylinders prepared with a mixture of just α-pinene and benzene as the internal standard. The current research discusses the testing of other cylinders and treatments for the potential of long-term stability of monoterpenes in a gas mixture. In this current study, a similar pattern of decreasing mole fraction, although somewhat improved short-term stability, was observed for ß-pinene and α-pinene, with growth of d-limonene, p-cymene, and camphene, in nickel-plated carbon steel cylinders. ß-Pinene and α-pinene showed excellent stability at over 6 months in aluminum cylinders treated with a different process (Experis) than used in the original study.

The National Institute of Standards and Technology ambient level methane in air Standard Reference Material historical record.

The National Institute of Standards and Technology (NIST) has been certifying lots, or series, of Standard Reference Materials (SRMs) containing ambient level methane in air for over 40 years. The historical record contains six traditional series of SRM 1658 (1 µmol mol(-1)), five of SRM 1660 (4 µmol mol(-1)), and seven of SRM 1659 (10 µmol mol(-1)) methane in air. All series of any one particular SRM can be linked to each other through the historical suites of gravimetric primary standard mixtures (PSMs) developed at NIST. One gas mixture cylinder from a series is chosen as the lot standard (LS), retained and held at NIST, and periodically compared to the PSMs to assure its stability. Recently, 6 of the original 18 LS still in service in the Gas Metrology Group inventory, and cylinder samples held at NIST from 6 other SRM lots, were analyzed against a newly prepared suite of PSMs using cavity ring-down spectroscopy. Data were analyzed using a generalized least squares linear regression. The results indicate that, within the original 95% confidence intervals, the methane concentration has remained the same for all the SRM LS and lot samples. The current predicted concentrations of the LS and samples for SRMs 1659 and 1660 are within 0.002 to 0.051 µmol mol(-1), or ≤0.5%, relative of the original certificate value. SRM 1658 LS and samples are within 0.0001 to 0.0023 µmol mol(-1), or ≤0.2% relative. These results illustrate the consistency, repeatability, and stability of these methane in air SRMs over the historical 35+-year record. It also demonstrates that the historical gravimetric primary methane in air suites have remained accurate and consistent over time.

NIST gravimetrically prepared atmospheric level methane in dry air standards suite.

The Gas Metrology Group at the National Institute of Standards and Technology was tasked, by a congressional climate change act, to support the atmospheric measurement community through standards development of key greenhouse gases. This paper discusses the development of a methane (CH(4)) primary standard gas mixture (PSM) suite to support CH(4) measurement needs over a large amount-of-substance fraction range 0.3-20,000 µmol mol(-1), but with emphasis at the atmospheric level 300-4000 nmol mol(-1). Thirty-six CH(4) in dry air PSMs were prepared in 5.9 L high-pressure aluminum cylinders with use of a time-tested gravimetric technique. Ultimately 14 of these 36 PSMs define a CH(4) standard suite covering the nominal ambient atmospheric range of 300-4000 nmol mol(-1). Starting materials of pure CH(4) and cylinders of dry air were exhaustively analyzed to determine the purity and air composition. Gas chromatography with flame-ionization detection (GC-FID) was used to determine a CH(4) response for each of the 14 PSMs where the reproducibility of average measurement ratios as a standard error was typically (0.04-0.26) %. An ISO 6134-compliant generalized least-squares regression (GenLine) program was used to analyze the consistency of the CH(4) suite. All 14 PSMs passed the u-test with residuals between the gravimetric and the GenLine solution values being between -0.74 and 1.31 nmol mol(-1); (0.00-0.16)% relative absolute. One of the 14 PSMs, FF4288 at 1836.16 ± 0.75 nmol mol(-1) (k = 1) amount-of-substance fraction, was sent to the Korea Research Institute of Standards and Science (KRISS), the Republic of Korea's National Metrology Institute, for comparison. The same PSM was subsequently sent to the National Oceanic and Atmospheric Administration (NOAA) for analysis to their standards. Results show agreement between KRISS-NIST of +0.13% relative (+2.3 nmol mol(-1)) and NOAA-NIST of -0.14% relative (-2.54 nmol mol(-1)).

Preparation of accurate, low-concentration gas cylinder standards by cryogenic trapping of a permeation tube gas stream.

National and international measurements are underpinned by accurate, low concentration standards. These standards are typically produced gravimetrically, or volumetrically, by a series of dilutions of the pure material by the balance gas. This blend technique is time-consuming and may involve the handling of pure, hazardous material. These problems have been overcome by developing a novel blend technique whereby the process gas stream, from an appropriate permeation tube, was cryogenically trapped in an aluminum cylinder. The permeation rate of the component is monitored by real time mass determinations using a magnetic suspension balance system. With the combination of the real-time calculated permeation rate, plus the use of a dilution system, a one step production of a very low concentration of the minor component in nitrogen gas can be achieved. This method was used to prepare low µmol/mol standards of propane, a known stable compound. Analysis of a conventional gravimetrically prepared 10 µmol/mol propane standard and a cryogenically prepared standard via a permeation gas stream resulted in agreement between the two of <0.1% at 10 µmol/mol, confirming the accuracy of the permeation method. After confirmation of the validity of the permeation/cryogenic trapping system, the propane permeation tube was replaced with a methyl mercaptan tube (a toxic, reactive compound) in balance nitrogen. After cryogenically trapping the methyl mercaptan output stream from the permeation system into a cylinder, the output stream and the cylinder gas mixture were analyzed. The results showed agreement of <0.6% for methyl mercaptan at 5, 10, 15, and 20 µmol/mol to the expected blend concentration, thereby demonstrating the validity of the method.

A Bayesian approach to the evaluation of comparisons of individually value-assigned reference materials.

Several recent international comparison studies used a relatively novel experimental design to evaluate the measurement capabilities of participating organizations. These studies compared the values assigned by each participant to one or more qualitatively similar materials with measurements made on all of the materials by one laboratory under repeatability conditions. A statistical model was then established relating the values to the repeatability measurements; the extent of agreement between the assigned value(s) and the consensus model reflected the participants' measurement capabilities. Since each participant used their own supplies, equipment, and methods to produce and value-assign their material(s), the agreement between the assigned value(s) and the model was a fairer reflection of their intrinsic capabilities than provided by studies that directly compared time- and material-constrained measurements on unknown samples prepared elsewhere. A new statistical procedure is presented for the analysis of such data. The procedure incorporates several novel concepts, most importantly a leave-one-out strategy for the estimation of the consensus value of the measurand, model fitting via Bayesian posterior probabilities, and posterior coverage probability calculation for the assigned 95% uncertainty intervals. The benefits of the new procedure are illustrated using data from the CCQM-K54 comparison of eight cylinders of n-hexane in methane.

Hydrocarbon gas standards at the pmol/mol level to support ambient atmospheric measurements.

Studies of climate change increasingly recognize the diverse influences exerted by hydrocarbons in the atmosphere, including roles in particulates and ozone formation. Measurements of key non-methane hydrocarbons (NMHCs) suggest atmospheric concentrations ranging from low pmol/mol to nmol/mol, depending on location and compound. To accurately establish concentration trends and to relate measurement records from many laboratories and researchers, it is essential to have good calibration standards. Several of the world's National Metrology Institutes (NMIs) are developing primary and secondary reference gas standards at the nmol/mol level. While the U.S. NMI, the National Institute of Standards and Technology (NIST), has developed pmol/mol standards for halocarbons and some volatile organics, the feasibility of preparing well-characterized, stable standards for NMHCs at the pmol/mol level is not yet established. NIST recently developed a suite of primary standards by gravimetric dilution that contains 18 NMHCs covering the concentration range of 60 pmol/mol to 230 pmol/mol. Taking into account the small but chemically significant contribution of NMHCs in the high-purity diluent nitrogen used in their preparation, the relative concentrations and short-term stability (2 to 3 months) of these NMHCs in the primary standards have been confirmed by chromatographic analysis. The gravimetric values assigned from the methods used to prepare the materials and the analytical concentrations determined from chromatographic analysis generally agree to within +/-2 pmol/mol. However, anomalous results for several of the compounds reflect the difficulties inherent in avoiding contamination and making accurate measurements at these very low levels.

Stability assessment of gas mixtures containing terpenes at nominal 5 nmol/mol contained in treated aluminum gas cylinders.

Studies of climate change increasingly recognize the diverse influences exerted by terpenes in the atmosphere, including roles in particulates, ozone formation, and their oxidizing potential. Measurements of key terpenes suggest atmospheric concentrations ranging from low pmol/mol (parts per trillion) to nmol/mol (parts per billion), depending on location and compound. To accurately establish concentration trends, assess the role of terpenes in atmospheric chemistry, and relate measurement records from many laboratories and researchers, it is essential to have good calibration standards. The feasibility of preparing well-characterized, stable gas cylinder standards for terpenes at the nmol/mol level is not yet well established. Several of the world's National Metrology Institutes (NMIs) are researching the feasibility of developing primary and secondary reference gas standards at the nmol/mol level for terpenes. The US NMI, the National Institute of Standards and Technology, has prepared several nmol/mol mixtures, in treated aluminum gas cylinders, containing terpenes in dry nitrogen at nominal 5 nmol/mol for stability studies. Overall, 11 terpenes were studied for stability. An initial gas mixture containing nine terpenes, one oxygenate, and six aromatic compounds, including benzene as an internal standard, was prepared. Results for four of the nine terpenes in this initial mixture indicate stability in these treated aluminum gas cylinders for over 6 months and project long term (years) stability. Interesting results were seen for beta-pinene, which when using a linear equation rate decline predicts that it will reach a zero concentration level at day 416. At the same time, increases in alpha-pinene, D: -limonene (R-(+)-limonene), and p-cymene were observed, including camphene, a terpene not prepared in the gas mixture, indicating a chemical transformation of beta-pinene to these species. Additional mixtures containing combination of either alpha-pinene, camphor, alpha-terpinene, and benzene indicate a second-order quadratic rate decline for the alpha-pinene and alpha-terpinene, a linear rate decline for camphor, and a second-order quadratic rate increase of camphene.

Gas standards development in support of NASA's sensor calibration program around the space shuttle.

The National Aeronautics and Space Administration (NASA) Kennedy Space Center (KSC) requires accurate gas mixtures containing argon (Ar), helium (He), hydrogen (H(2)), and oxygen (O(2)) in a balance of nitrogen (N(2)) to calibrate mass spectrometer-based sensors used around their manned and unmanned space vehicles. This also includes space shuttle monitoring around the launch area and inside the shuttle cabin. NASA was in need of these gas mixtures to ensure the safety of the shuttle cabin and the launch system. In 1993, the National Institute of Standards and Technology (NIST) was contracted by NASA to develop a suite of primary standard mixtures (PSMs) containing helium, hydrogen, argon, and oxygen in a balance gas of nitrogen. NIST proceeded to develop a suite of 20 new gravimetric primary PSMs. At the same time NIST contracted Scott Specialty Gases (Plumsteadville, PA) to prepare 18 cylinder gas mixtures which were then sent to NIST. NIST used their newly prepared PSMs to assign concentration values ranging from 100 to 10,000 micromol/mol with relative expanded uncertainties (95% confidence interval) of 0.8-10% to the 18 Scott Specialty Gases prepared mixtures. A total of 12 of the mixtures were sent to NASA as NIST traceable standards for calibration of their mass spectrometers. The remaining 6 AIRGAS mixtures were retained at NIST. In 2006, these original 12 gas standards at NASA had become low in pressure and additionally NASA needed a lower concentration level; therefore, NIST was contracted to certify three new sets of gas standards. NIST prepared a new suite of 22 PSMs with weighing uncertainties of <0.1%. These 22 PSMs were compared to some of the original 20 PSMs developed in 1993 and with the NIST valued assigned Scott Specialty Gas mixtures that NIST had retained. Results between the two suites of primary standards and the 1993 NASA mixtures agreed, verifying their stability. At the same time, NASA contracted AIRGAS (Chicago, Illinois) to prepare 45 cylinder gas mixtures which were then sent to NIST. Each of the 3 sets of standards contained 15 cylinder gas mixtures: set no. 1, He at 12,000 micromol/mol, H(2) at 600 micromol/mol, Ar at 100 micromol/mol, and O(2) at 600 micromol/mol; set no. 2, He at 15 000 micromol/mol, H(2) at 5000 micromol/mol, Ar at 1000 micromol/mol, O(2) at 5000 micromol/mol; and set no. 3, He at 50 micromol/mol, H(2), Ar, and O(2) each at 25 micromol/mol with a balance gas of N(2). NIST used their newly prepared primary standards to assign concentration values to each component in these three new mixture sets to relative expanded uncertainties of 0.5-2.2%. The NIST certified AIRGAS prepared mixtures were then sent to NASA to use as "working standards" to calibrate their mass spectrometers (MSs).

Stability of gaseous volatile organic compounds contained in gas cylinders with different internal wall treatments.

Measurements of volatile organic compounds (VOCs) have been ongoing for decades to track growth rates and assist in curbing emissions of these compounds into the atmosphere. To accurately establish mole fraction trends and assess the role of these gas-phase compounds in atmospheric chemistry it is essential to have good calibration standards. A necessity and precursor to accurate VOC gas standards are the gas cylinders and the internal wall treatments that aid in maintaining the stability of the mixtures over long periods of time, measured in years. This paper will discuss the stability of VOC gas mixtures in different types of gas cylinders and internal wall treatments. Stability data will be given for 85 VOCs studied in gas mixtures by National Metrology Institutes and other agency laboratories. This evaluation of cylinder treatment materials is the outcome of an activity of the VOC Expert Group within the framework of the World Meteorological Organization (WMO) Global Atmospheric Watch (GAW) program.

Differences between propane in nitrogen versus air matrix analyzed using gas chromatography with flame-ionization detection.

New US Federal low-level automobile emission requirements, such as Zero Level Emission Vehicle (ZLEV), for hydrocarbons and other species have resulted in manufacturers need for new certified reference materials. The new emission requirement for hydrocarbons requires the use, by automobile manufacturing testing facilities, of 100 nmol/mol (ppb) propane in air gas standard. Emission measurement instruments are required, by Federal law, to be calibrated with the US National Institute of Standards and Technology (NIST) traceable reference materials. A NIST Standard Reference Material (SRM) containing 100 nmol/mol propane has been developed. During the development of this SRM a critical question arose as to the matrix of the primary propane standards. The automobile companies make their measurements using total hydrocarbon analyzers with flame-ionization detectors which integrate all hydrocarbons in a sample. NIST uses gas chromatography/flame-ionization detection (GC/FID) with a column to separate all components. Since the SRM mixtures were in air, the question as to the effect of oxygen on the detector arose. To investigate this effect, two suites of propane primary standards were developed: one in air and the other in nitrogen. The two suites of primary standards were analyzed using NIST methods, and the concentration of propane in an air mixture was determined. The results show that there was a difference of 0.63% in the propane concentration determined versus air and nitrogen suites.

Comparison of halocarbon measurements in an atmospheric dry whole air sample.

The growing awareness of climate change/global warming, and continuing concerns regarding stratospheric ozone depletion, will require continued measurements and standards for many compounds, in particular halocarbons that are linked to these issues. In order to track atmospheric mole fractions and assess the impact of policy on emission rates, it is necessary to demonstrate measurement equivalence at the highest levels of accuracy for assigned values of standards. Precise measurements of these species aid in determining small changes in their atmospheric abundance. A common source of standards/scales and/or well-documented agreement of different scales used to calibrate the measurement instrumentation are key to understanding many sets of data reported by researchers. This report describes the results of a comparison study among National Metrology Institutes and atmospheric research laboratories for the chlorofluorocarbons (CFCs) dichlorodifluoromethane (CFC-12), trichlorofluoromethane (CFC-11), and 1,1,2-trichlorotrifluoroethane (CFC-113); the hydrochlorofluorocarbons (HCFCs) chlorodifluoromethane (HCFC-22) and 1-chloro-1,1-difluoroethane (HCFC-142b); and the hydrofluorocarbon (HFC) 1,1,1,2-tetrafluoroethane (HFC-134a), all in a dried whole air sample. The objective of this study is to compare calibration standards/scales and the measurement capabilities of the participants for these halocarbons at trace atmospheric levels. The results of this study show agreement among four independent calibration scales to better than 2.5% in almost all cases, with many of the reported agreements being better than 1.0%.