Effect of carrier gas on the gas sensing performance of Co12xNixMnxFe2yCeyO4 double-substitution spinel in flammable gases and volatile organic compounds

The presence of high concentrations of flammable gases and volatile organic compounds in the atmosphere has been widely reported to be detrimental to human survival. A lot of research effort has been put toward finding an efficient means of quick detection of these gases below their ‘immediately dangerous to life or health’ concentrations. Detecting these gases in an oxygendeficient environment is a crucial task to consider and has been overlooked. In this research, doublesubstitution spinel with the chemical formula Co12xNixMnxFe2yCeyO4, where 0 x = y 0.3, was prepared via the glycol-thermal technique. The final products, following appropriate substitution, were CoFe2O4 (dried naturally), CoFe2O4 (dried with infrared lamp), Co0.8Ni0.1Mn0.1Fe1.9Ce0.1O4, Co0.6Ni0.2Mn0.2Fe1.8Ce0.2O4 and Co0.4Ni0.3Mn0.3Fe1.7Ce0.3O4 spinel ferrites. The X-ray diffractometry (XRD), high-resolution transmission electron micrographs (HRTEM) and X-ray photoelectron spectroscopy (XPS) of the samples confirmed the formation of the spinel. The gas sensing performance of these samples was tested at the operating temperature of 225 C toward liquefied petroleum gas (LPG), ammonia, ethanol and propanol. The Co0.8Ni0.1Mn0.1Fe1.9Ce0.1O4-based sensor was selective to LPG, with a high response of 116.43 toward 6000 ppm of LPG when helium was used as the carrier gas, 3.35 when dry air was the carrier gas, 4.4 when nitrogen was the carrier gas, but it was not sensitive when argon was used as the carrier gas.https://www.mdpi.com/journal/coatingsam2024PhysicsNon

Development of benzene, toluene, ethyl benzene, m-xylene, p-xylene and o-xylene (BTEX) gas reference standards for air pollution monitoring in South Africa

Direct monitoring of volatile organic compounds emitted from industrial sources as well as the monitoring of ambient levels thereof in the atmosphere play an important role in providing data for various legislative requirements. There are many volatile organic compounds emitted to the atmosphere, from biomass burning, power stations, and many other sources. Primary reference gas mixtures of volatile organic compounds containing six components, namely benzene, toluene, ethylbenzene, o-xylene, m-xylene, and p-xylene (BTEX) were prepared by gravimetric methods at nominal amount of substance fractions of 10 µmol/mol. The preparation was performed using the stainless steel (loop) method and direct liquid injection method using gas tight syringe connected to a dedicated syringe heater for comparison purposes. The results of the gravimetric values for both methods were within 1 % of the nominal amount of substance fraction. After the preparation, comparison was achieved by analysis of the BTEX gas mixtures using gas chromatography with flame ionisation detection (GC-FID) and showed comparability to within 2 % of the gravimetric values. The contributions to the uncertainty of measurement were from weighing stainless steel tubes, syringes, and gas cylinders, as well as purity data. The contribution to the uncertainty of measurement from the analysis by GC-FID were repeatability and reproducibility. The combined expanded uncertainty of measurement was between 1.09 % and 3.51 %. The larger deviation from the gravimetric values and associated uncertainty was observed for benzene due to its higher volatility compared to the other components. The BTEX reference gas mixtures prepared in this study are currently being used as a source of traceability in South Africa for air pollution monitoring purposes.Open access funding provided by Mintek.http://link.springer.com/journal/769Chemistr

CCQM-K120 (Carbon dioxide at background and urban level)

CCQM-K120.a comparison involves preparing standards of carbon dioxide in air which are fit for purpose for the atmospheric monitoring community, with stringent requirements on matrix composition and measurement uncertainty of the CO2 mole fraction. This represents an analytical challenge and is therefore considered as a Track C comparison. The comparison will underpin CMC claims for CO2 in air for standards and calibrations services for the atmospheric monitoring community, matrix matched to real air, over the mole fraction range of 250 μmol/mol to 520 μmol/mol. CCQM-K120.b comparison tests core skills and competencies required in gravimetric preparation, analytical certification and purity analysis. It is considered as a Track A comparison. It will underpin CO2 in air and nitrogen claims in a mole fraction range starting at the smallest participant's reported expanded uncertainty and ending at 500 mmol/mol. Participants successful in this comparison may use their result in the flexible scheme and underpin claims for all core mixtures This study has involved a comparison at the BIPM of a suite of 44 gas standards prepared by each of the participating laboratories. Fourteen laboratories took part in both comparisons (CCQM-K120.a, CCQM-K120.b) and just one solely in the CCQM-K120.b comparison. The standards were sent to the BIPM where the comparison measurements were performed. Two measurement methods were used to compare the standards, to ensure no measurement method dependant bias: GC-FID and FTIR spectroscopic analysis corrected for isotopic variation in the CO2 gases, measured at the BIPM using absorption laser spectroscopy. Following the advice of the CCQM Gas Analysis Working Group, results from the FTIR method were used to calculate the key comparison reference values