scholarly journals Numerical Modeling of Volatile Organic Compounds (VOC) Emissions during Preheating of Magnesia-Carbon Bricks in a Basic Oxygen Furnace

Metals ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1277
Author(s):  
Soumitra Kumar Dinda ◽  
Kinnor Chattopadhyay
Keyword(s):  
Mathematical Model ◽  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Basic Oxygen Furnace ◽  
Chemical Thermodynamics ◽  
Transfer Model ◽  
Emission Rates ◽  
Basic Oxygen ◽  
Voc Emissions ◽  
Volatile Organic

The refractory preheating process in oxygen furnaces is a dynamic input of energy in a chemically complex system requiring special attention to chemical emissions relative to permissible release limits. This particular industrial and regulatory interest is the emission of volatile organic compounds (VOC), given their detrimental impacts on human health. In the present work, a mathematical model was developed to predict the emission rates of volatile organics during the preheating of a 260-ton basic oxygen furnace. A numerical heat transfer model was developed using finite difference techniques to obtain the thermal profile and then integrated with chemical thermodynamics using FactSage 7.0 (CRCT, Polytechnique Montreal Quebec Canada, H3C 3A7). The parameters that affected VOC emissions were preheating process times, burner gas composition, heating rate, and burner geometry. Two different preheating procedures were compared, and emission rates were predicted with extended use of a top burner providing the greatest degree of emissions control. The mathematical model was validated against plant data with respect to average emission rates of CO, CO2, SOX, and NOX.

scholarly journals Surface–atmosphere fluxes of volatile organic compounds in Beijing

2020 ◽  
Vol 20 (23) ◽  
pp. 15101-15125
Author(s):  
W. Joe F. Acton ◽  
Zhonghui Huang ◽  
Brian Davison ◽  
Will S. Drysdale ◽  
Pingqing Fu ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Emission Inventory ◽  
Central Area ◽  
High Reactivity ◽  
Emission Rates ◽  
Voc Emissions ◽  
Formation Potential ◽  
Surface Atmosphere ◽  
Volatile Organic

Abstract. Mixing ratios of volatile organic compounds (VOCs) were recorded in two field campaigns in central Beijing as part of the Air Pollution and Human Health in a Chinese Megacity (APHH) project. These data were used to calculate, for the first time in Beijing, the surface–atmosphere fluxes of VOCs using eddy covariance, giving a top-down estimation of VOC emissions from a central area of the city. The results were then used to evaluate the accuracy of the Multi-resolution Emission Inventory for China (MEIC). The APHH winter and summer campaigns took place in November and December 2016 and May and June 2017, respectively. The largest VOC fluxes observed were of small oxygenated compounds such as methanol, ethanol + formic acid and acetaldehyde, with average emission rates of 8.31 ± 8.5, 3.97 ± 3.9 and 1.83 ± 2.0 nmol m−2 s−1, respectively, in the summer. A large flux of isoprene was observed in the summer, with an average emission rate of 5.31 ± 7.7 nmol m−2 s−1. While oxygenated VOCs made up 60 % of the molar VOC flux measured, when fluxes were scaled by ozone formation potential and peroxyacyl nitrate (PAN) formation potential the high reactivity of isoprene and monoterpenes meant that these species represented 30 % and 28 % of the flux contribution to ozone and PAN formation potential, respectively. Comparison of measured fluxes with the emission inventory showed that the inventory failed to capture the magnitude of VOC emissions at the local scale.

scholarly journals Species and characteristics of volatile organic compounds emitted from an auto-repair painting workshop

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
M. Y. Song ◽  
H. Chun
Keyword(s):  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Large Scale ◽  
Butyl Acetate ◽  
Small Scale ◽  
Indoor Environments ◽  
Voc Emissions ◽  
Volatile Organic ◽  
Before And After ◽  
Adsorption Systems

AbstractVolatile organic compounds (VOCs) are secondary pollutant precursors having adverse impacts on the environment and human health. Although VOC emissions, their sources, and impacts have been investigated, the focus has been on large-scale industrial sources or indoor environments; studies on relatively small-scale enterprises (e.g., auto-repair workshops) are lacking. Here, we performed field VOC measurements for an auto-repair painting facility in Korea and analyzed the characteristics of VOCs emitted from the main painting workshop (top coat). The total VOC concentration was 5069–8058 ppb, and 24–35 species were detected. The VOCs were mainly identified as butyl acetate, toluene, ethylbenzene, and xylene compounds. VOC characteristics differed depending on the paint type. Butyl acetate had the highest concentration in both water- and oil-based paints; however, its concentration and proportion were higher in the former (3256 ppb, 65.5%) than in the latter (2449 ppb, 31.1%). Comparing VOC concentration before and after passing through adsorption systems, concentrations of most VOCs were lower at the outlets than the inlets of the adsorption systems, but were found to be high at the outlets in some workshops. These results provide a theoretical basis for developing effective VOC control systems and managing VOC emissions from auto-repair painting workshops.

scholarly journals Water-Enhanced Flux Changes under Dynamic Temperatures in the Vertical Vapor-Phase Diffusive Transport of Volatile Organic Compounds in Near-Surface Soil Environments

2021 ◽  
Vol 13 (12) ◽  
pp. 6570
Author(s):  
Asma Akter Parlin ◽  
Monami Kondo ◽  
Noriaki Watanabe ◽  
Kengo Nakamura ◽  
Mizuki Yamada ◽  
...  
Keyword(s):  
Air Quality ◽  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Vapor Phase ◽  
Inverse Correlation ◽  
Diffusive Transport ◽  
Near Surface ◽  
Voc Emissions ◽  
Transport Behavior ◽  
Volatile Organic

The quantitative understanding of the transport behavior of volatile organic compounds (VOCs) in near-surface soils is highly important in light of the potential impacts of soil VOC emissions on the air quality and climate. Previous studies have suggested that temperature changes affect the transport behavior; however, the effects are not well understood. Indeed, much larger changes in the VOC flux under in situ dynamic temperatures than those expected from the temperature dependence of the diffusion coefficients of VOCs in the air have been suggested but rarely investigated experimentally. Here, we present the results of a set of experiments on the upward vertical vapor-phase diffusive transport of benzene and trichloroethylene (TCE) in sandy soils with water contents ranging from an air-dried value to 10 wt% during sinusoidal temperature variation between 20 and 30 °C. In all experiments, the flux from the soil surface was correlated with the temperature, as expected. However, the changes in flux under wet conditions were unexpectedly large and increased with increasing water content; they were also larger for TCE, the volatility of which depended more strongly on the temperature. Additionally, the larger flux changes were accompanied by a recently discovered water-induced inverse correlation between temperature and flux into the overlying soil. These results demonstrated that the flux changes of VOCs under dynamic temperatures could be increased by volatilization-dissolution interactions of VOCs with water. Future extensive studies on this newly discovered phenomenon would contribute to a better understanding of the impacts of soil VOC emissions on the air quality and climate.

scholarly journals Fluxes and concentrations of volatile organic compounds from a South-East Asian tropical rainforest

2010 ◽  
Vol 10 (17) ◽  
pp. 8391-8412 ◽  
Author(s):  
B. Langford ◽  
P. K. Misztal ◽  
E. Nemitz ◽  
B. Davison ◽  
C. Helfter ◽  
...  
Keyword(s):  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Tropical Forests ◽  
Atmospheric Chemistry ◽  
Carbon Flux ◽  
Tropical Rainforest ◽  
East Asian ◽  
Emission Rates ◽  
Reactive Carbon ◽  
Volatile Organic

Abstract. As part of the OP3 field study of rainforest atmospheric chemistry, above-canopy fluxes of isoprene, monoterpenes and oxygenated volatile organic compounds were made by virtual disjunct eddy covariance from a South-East Asian tropical rainforest in Malaysia. Approximately 500 hours of flux data were collected over 48 days in April–May and June–July 2008. Isoprene was the dominant non-methane hydrocarbon emitted from the forest, accounting for 80% (as carbon) of the measured emission of reactive carbon fluxes. Total monoterpene emissions accounted for 18% of the measured reactive carbon flux. There was no evidence for nocturnal monoterpene emissions and during the day their flux rate was dependent on both light and temperature. The oxygenated compounds, including methanol, acetone and acetaldehyde, contributed less than 2% of the total measured reactive carbon flux. The sum of the VOC fluxes measured represents a 0.4% loss of daytime assimilated carbon by the canopy, but atmospheric chemistry box modelling suggests that most (90%) of this reactive carbon is returned back to the canopy by wet and dry deposition following chemical transformation. The emission rates of isoprene and monoterpenes, normalised to 30 °C and 1000 μmol m−2 s−1 PAR, were 1.6 mg m−2 h−1 and 0.46mg m−2 h−1 respectively, which was 4 and 1.8 times lower respectively than the default value for tropical forests in the widely-used MEGAN model of biogenic VOC emissions. This highlights the need for more direct canopy-scale flux measurements of VOCs from the world's tropical forests.

Selected problems concerning volatile organic compounds emission reduction from thick-veneer pine plywood

2020 ◽  
Vol 111 ◽  
pp. 131-20
Author(s):  
Martyna Dyrwal ◽  
Piotr Borysiuk
Keyword(s):  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Carbonyl Compounds ◽  
Emission Reduction ◽  
Caproic Acid ◽  
Emission Rates ◽  
Wood Material ◽  
Soaking Time ◽  
Volatile Organic ◽  
Higher Temperature

Selected problems concerning volatile organic compounds emission reduction from thick-veneer pine plywood. The paper presents results of research conducted on volatile organic compounds emissions, considering two different production parameter sets for thick-veneer pine plywood, manufactured in industrial conditions. Both types of plywood were produced from raw wood material, which was hydrothermally treated under two different variants of parameters (I – 47˚C, 19 h; II – 55˚C, 24 h). Based on the results it was stated that severe hydrothermal treatment of raw wood material (longer soaking time, higher temperature) had impact on reduction of plywood VOC emission rates. Main VOCs emitted from pine plywood were monoterpenes and carbonyl compounds. Of the monoterpenes, α-pinene and 3-carene had the highest emission. Of the carbonyl group of compounds, the highest emission had hexanal and caproic acid.

First Comprehensive Measurements of Emission Rates of Greenhouse Gases, Volatile Organic Compounds and Reduced Sulfur Compounds from a Tailings Pond in the Alberta Oil Sands

2020 ◽  
Author(s):  
Ralf Staebler ◽  
Samar Moussa ◽  
Yuan You ◽  
Hayley Hung ◽  
Maryam Moradi ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Volatile Organic Compounds ◽  
Organic Compounds ◽  
Oil Sands ◽  
Regulatory Compliance ◽  
Sulfur Compounds ◽  
Emission Rates ◽  
Reduced Sulfur Compounds ◽  
Volatile Organic ◽  
Reduced Sulfur

<p>Canada’s Oil Sands Region in northern Alberta contains the world’s largest deposits of commercially exploited bitumen. Extraction of synthetic crude oil from these deposits is a water intensive process, requiring large ponds for water recycling and/or final storage of tailings, already covering a total of over 100 km<sup>2</sup> of liquid surface area in the Athabasca Oil sands. The primary extraction tailings ponds primarily contain sand, silt, clay and unrecovered bitumen, while a few secondary extraction ponds also receive solvents and inorganic and organic by-products of the extraction process. Fugitive emissions of pollutants from these ponds to the atmosphere may therefore be a concern, but until recently, data on emission rates for many pollutants, other than a few reported under regulatory compliance monitoring, were sparse. We present here the results from a comprehensive field campaign to quantify the emissions from a secondary extraction pond to the atmosphere of 68 volatile organic compounds (VOCs), 22 polycyclic aromatic compounds (PACs), 8 reduced sulfur compounds as well as methane, carbon dioxide and ammonia. Three micrometeorological flux methods (eddy covariance, vertical gradients and inverse dispersion modeling) were evaluated for methane fluxes to ensure their mutual comparability. Methane and carbon dioxide fluxes were similar to previous results based on flux chamber measurements. Emission rates for 12 PACs, alkanes and aromatic VOCs, several sulfur species, and ammonia were found to be significant. PACs were dominated by methyl naphthalenes and phenanthrenes, while diethylsulfide and  and n-heptane were the dominant reduced sulfur and VOC species, respectively. The role of these previously unavailable emission rates in regional pollutant budgets will be discussed.</p>

scholarly journals From emissions to ambient mixing ratios: on-line seasonal field measurements of volatile organic compounds over a Norway spruce dominated forest in central Germany

2013 ◽  
Vol 13 (11) ◽  
pp. 30187-30232 ◽  
Author(s):  
E. Bourtsoukidis ◽  
J. Williams ◽  
J. Kesselmeier ◽  
S. Jacobi ◽  
B. Bonn
Keyword(s):  
Volatile Organic Compounds ◽  
Norway Spruce ◽  
Organic Compounds ◽  
Atmospheric Chemistry ◽  
Temperature Dependency ◽  
Emission Rates ◽  
Temperature Dependent ◽  
Central Germany ◽  
Mixing Ratios ◽  
Volatile Organic

Abstract. Biogenic volatile organic compounds (BVOC) are substantial contributors to atmospheric chemistry and physics and demonstrate the close relationship between biosphere and atmosphere. Their emission rates are highly sensitive to meteorological and environmental changes with concomitant impacts on atmospheric chemistry. We have investigated seasonal isoprenoid and oxygenated VOC (oxVOC) fluxes from a Norway spruce (Picea abies) tree in Central Germany and explored the emission responses under various atmospheric conditions. Emission rates were quantified by using dynamic branch enclosure and Proton Transfer Reaction–Mass Spectrometry (PTR-MS) techniques. Additionally, ambient mixing ratios were derived through application of a new box model treatment on the dynamic chamber measurements. These are compared in terms of abundance and origin with the corresponding emissions. Isoprenoids govern the BVOC emissions from Norway spruce, with monoterpenes and sesquiterpenes accounting for 50.8 ± 7.2% and 19.8 ± 8.1% respectively of the total emissions. Normalizing the VOC emission rates, we have observed a trend of reduction of carbon containing emissions from April to November, with an enhancement of oxVOC. Highest emission rates were observed in June for all measured species, with the exception of sesquiterpenes that were emitted most strongly in April. We exploit the wide range of conditions experienced at the site to filter the dataset with a combination of temperature, ozone and absolute humidity values in order to derive the emission potential and temperature dependency development for the major chemical species investigated. A profound reduction of monoterpene emission potential (E30) and temperature dependency (β) was found under low temperature regimes, combined with low ozone levels (E30MT, LTLO3=56 ± 9.1 ng g(dw)−1 h−1, βMT,LTLO3=0.03±0.01 K−1) while a combination of both stresses was found to alter their emissions responses with respect to temperature substantially (E30MT,HTHO3=1420.1 ± 191.4 ng g(dw)−1 h−1, βMT,HTHO3=0.15 ± 0.02 K−1). Moreover, we have explored compound relationships under different atmospheric condition sets, addressing possible co-occurrence of emissions under specific conditions. Finally, we evaluate the temperature dependent algorithm that seems to describe the temperature dependent emissions. Highest emission deviations were observed for monoterpenes and these emission fluctuations were attributed to a fraction which is triggered by an additional light dependency.

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