Photoinduced Evolutions of Permafrost-Derived Carbon in Subarctic Thermokarst Pond Surface Waters.

In subarctic regions, rising temperature and permafrost thaw lead to the formation of thermokarst ponds, where organics from eroding permafrost accumulate. Despite its environmental significance, limited knowledge exists regarding the photosensitivity of permafrost-derived carbon in these ponds. In this study, laboratory experiments were conducted to explore the photochemical transformations of organic matter in surface water samples from thermokarst ponds from different environments in northern Quebec, Canada.

Ozonolysis of 2-Methyl-2-pentenal: New Insights from Master Equation Modeling.

Experimental and theoretical studies were carried out to investigate the ozonolysis of -2-methyl-2-pentenal. The experiments were conducted in atmospheric simulation chambers coupled to a Fourier transform infrared (FTIR) spectrometer and a gas chromatograph-mass spectrometer at room temperature and atmospheric pressure in the presence of an excess of cyclohexane in dry conditions (RH < 1%). The ozonolysis reaction was investigated theoretically from the results of accurate density functional (M06-2X) and ab initio [CCSD(T)] computations, employing the AVTZ basis set.

Sunlight Induces the Production of Atmospheric Volatile Organic Compounds (VOCs) from Thermokarst Ponds.

Ground subsidence caused by permafrost thawing causes the formation of thermokarst ponds, where organic compounds from eroding permafrost accumulate. We photolyzed water samples from two such ponds in Northern Quebec and discovered the emission of volatile organic compounds (VOCs) using mass spectrometry. One pond near peat-covered permafrost mounds was organic-rich, while the other near sandy mounds was organic-poor.

Indoor heterogeneous photochemistry of molds and their contribution to HONO formation.

To better understand the impact of molds on indoor air quality, we studied the photochemistry of microbial films made by Aspergillus niger species, a common indoor mold. Specifically, we investigated their implication in the conversion of adsorbed nitrate anions into gaseous nitrous acid (HONO) and nitrogen oxides (NO ), as well as the related VOC emissions under different indoor conditions, using a high-resolution proton transfer reaction-time of flight-mass spectrometer (PTR-TOF-MS) and a long path absorption photometer (LOPAP). The different mold preparations were characterized by the means of direct injection into an Orbitrap high-resolution mass spectrometer with a heated electrospray ionization (ESI-Orbitrap-MS).

Indoor heterogeneous photochemistry of furfural drives emissions of nitrous acid.

People spend approximately 80% of their time indoor, making the understanding of the indoor chemistry an important task for safety. The high surface-area-to-volume ratio characteristic of indoor environments leads the semi-volatile organic compounds (sVOCs) to deposit on the surfaces. Using a long path absorption photometer (LOPAP), this work investigates the formation of nitrous acid (HONO) through the photochemistry of adsorbed nitrate anions and its enhancement by the presence of furfural.

Influence of indoor chemistry on the emission of mVOCs from Aspergillus niger molds.

People spend 80% of their time indoors exposed to poor air quality due to mold growth in humid air as well as human activities (painting, cooking, cleaning, smoking…). To better understand the impact of molds on indoor air quality, we studied the emission of microbial Volatile Organic Compounds (mVOCs) from Aspergillus niger, cultivated on malt agar extract, using a high-resolution proton transfer reaction- time of flight- mass spectrometer (PTR-TOF-MS). These emissions were studied for different cultivation time and indoor relative humidities.

Gas-phase UV absorption spectra and OH-oxidation kinetics of 1-1,2,3-triazole and pyrazole.

In this work, we report the gas phase UV absorption spectra and the kinetics of the OH-oxidation of 1-1,2,3-triazole and pyrazole. UV spectra were determined between 200 and 250 nm, at 350 ± 2 K and at pressures between 0.09 and 0.