Publications by authors named "Romeo I Olariu"

Urbanization and industrialization are important transformations shaping the current statement of the society, enhancing significantly the combustion emissions which are threatening the global climate system, air quality, and human health. These emissions contain polycyclic aromatic hydrocarbons (PAHs) which are well known for their high toxicity. The present study is the first assessing the seasonal variation of 17 PAHs in size segregated fractions of atmospheric aerosol particles from a Romanian metropolitan area.

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Methyl-butenols are a category of oxygenated biogenic volatile organic compounds emitted by plants as part of their natural metabolic processes. This study examines the gas-phase reactions of ozone (O) with five methyl-butenols (2-methyl-3-buten-2-ol, 3-methyl-2-buten-1-ol, 3-methyl-3-buten-1-ol, 2-methyl-3-buten-1-ol, and 3-methyl-3-buten-2-ol) under atmospheric conditions at a temperature of (298 ± 2) K and pressure of (1000 ± 10) mbar. The experimental values for the gas-phase reaction rate coefficients obtained in this study, by using the relative rate method, are as follows (in cm molecule s): k(3-methyl-2-buten-1-ol + O) = (311 ± 20) × 10, (2-methyl-3-buten-2-ol + O) = (9.

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Five biogenic unsaturated alcohols have been investigated under simulated atmospheric conditions regarding their gas-phase OH reactivity. The gas-phase rate coefficients of OH radicals with 2-methyl-3-buten-2-ol (), 3-methyl-2-buten-1-ol (), 3-methyl-3-buten-1-ol (), 2-methyl-3-buten-1-ol (), and 3-methyl-3-buten-2-ol () at 298 ± 2 K and 1000 ± 10 mbar total pressure of synthetic air were determined under low- and high-NO conditions using the relative kinetic technique. The present work provides for the first time the rate coefficients of gas-phase reactions of hydroxyl radicals with 2-methyl-3-buten-1-ol and 3-methyl-3-buten-2-ol.

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The present study provides a comprehensive assessment of the quantitative analysis by high-performance liquid chromatography coupled with dual orthogonal electrospray ionization time-of-flight mass spectrometry (HPLC-ESI-TOF-MS) of pinene markers, biomass-burning related phenols, and other relevant carboxylic acids in atmospheric aerosol samples. Significant insights into the quantitative determination are offered on the basis of systematic experiments targeting the optimization of chromatographic separation, ionization source, and mass spectrometer performance. After testing three analytical columns, the best separation of the compounds of interest was achieved on a Poroshell 120 ECC18 column (4.

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The present study reports first data on the organic molecular composition and evolution of secondary organic aerosols (SOAs) markers in aerosol samples from an urban environment in Romania. Targeted and non-targeted approaches of liquid chromatography tandem with time-of-flight mass spectrometry (LC-ToF-MS) were used as powerful analytical approaches for aerosol characterization at the molecular level. Four distinct organic molecular groups (CHO, CHON, CHONS, and CHOS) were classified as relevant for both warm (with 847 assigned molecular formulae) and cold (with 432 assigned molecular formulae) periods.

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Partitioning between surface waters and the atmosphere is an important process, influencing the fate and transport of semi-volatile contaminants. In this work, a simple methodology that combines experimental data and modeling was used to investigate the degradation of a semi-volatile pollutant in a two-phase system (surface water + atmosphere). 4-Isobutylacetophenone (IBAP) was chosen as a model contaminant; IBAP is a toxic transformation product of the non-steroidal, anti-inflammatory drug ibuprofen.

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Unsaturated alcohols are volatile organic compounds (VOCs) that characterize the emissions of plants. Changes in climate together with related increases of biotic and abiotic stresses are expected to increase these emissions in the future. Ozonolysis is one of the oxidation pathways that control the fate of unsaturated alcohols in the atmosphere.

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Chemical analysis was performed on sediment samples collected in two sampling sessions (July and October) from Podu Iloaiei Dam Lake, one of the most important water resources used for aquaculture in north-eastern Romania. The concentration of 15 trace elements (TEs), 8 refractory elements (REs), and 15 rare earth elements (REEs)-determined using inductively coupled plasma mass spectrometry-showed variability largely dependent of the sampling points and collection time. Manganese was the most abundant TE, V and Cr were the most abundant REs, while Ce was one of the most abundant REEs.

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The present paper reports the first size-resolved element measurements in the PM fraction collected throughout 2016 in the Iasi urban area in north-eastern Romania. Concentrations of water-soluble elements (Ag, Al, As, B, Ba, Be, Bi, Cd, Co, Cu, Cr, Fe, Ga, Mg, Mn, Mo, Ni, Pb, Rb, Se, Sr, Te, Ti, U, V, Zn) were determined using inductively coupled plasma mass spectrometry. Several water-soluble heavy metals (Al, Fe, Zn, As, Cr, Pb) exhibit clear seasonal patterns with maxima over the cold season and minima over the warm season.

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Recently, there is growing attention on the use of low-cost sorbents in the depollution of contaminated waters. As a consequence, the present work investigates the potential of soy bran and mustard husk as possible sorbent for the removal of arsenic(V) from residual water. Effects of various operating parameters such as: contact time, pH, initial arsenic concentration, pH, sorbent dose, temperature were investigated to determine the removal efficiency of arsenic(V).

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We study the gas-phase pyrolysis of benzyl azide (BA, C6H5CH2N3) using ultraviolet photoelectron spectroscopy (UVPES) and matrix-isolation infrared (IR) spectroscopy, together with electronic structure calculations and Rice-Ramsperger-Kassel-Marcus (RRKM) calculations. It is found that BA decomposes via N2 elimination at ca. 615 K, primarily yielding benzenemethaninime.

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A new flow reactor has been developed to study ozonolysis reactions at ambient pressure and room temperature (297 ± 2 K). The reaction kinetics of O(3) with 4-methyl-1-pentene (4M1P), 2-methyl-2-pentene (2M2P), 2,4,4-trimethyl-1-pentene (tM1P), 2,4,4-trimethyl-2-pentene (tM2P) and α-pinene have been investigated under pseudo-first-order conditions. Absolute measurements of the rate coefficients have been carried out by recording O(3) consumption in excess of organic compound.

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