scholarly journals Assessing poorly crystalline and mineral-organic species by extracting Al, Fe, Mn, and Si using (citrate-) ascorbate and oxalate

Geoderma ◽  
2021 ◽  
Vol 397 ◽  
pp. 115095
Author(s):  
Thilo Rennert ◽  
Jan Dietel ◽  
Stefan Heilek ◽  
Reiner Dohrmann ◽  
Tim Mansfeldt
Keyword(s):  
2017 ◽  
Author(s):  
Thilina Jayarathne ◽  
Chelsea E. Stockwell ◽  
Prakash V. Bhave ◽  
Puppala S. Praveen ◽  
Chathurika M. Rathnayake ◽  
...  

Abstract. The Nepal Ambient Monitoring and Source Testing Experiment (NAMaSTE) characterized widespread and under-sampled combustion sources common to South Asia, including brick kilns, garbage burning, diesel and gasoline generators, diesel groundwater pumps, idling motorcycles, traditional and modern cooking stoves and fires, crop residue burning, and a heating fire. Fuel-based emission factors (EF; with units of pollutant mass emitted per kg of fuel combusted) were determined for fine particulate matter (PM2.5), organic carbon (OC), elemental carbon (EC), inorganic ions, trace metals, and organic species. For the forced draught zig-zag brick kiln, EFPM2.5 ranged 1–19 g kg−1 with major contributions from OC (7 %), sulfate expected to be in the form of sulfuric acid (31.9 %), and other chemicals not measured (e.g., particle bound water). For the clamp kiln, EFPM2.5 ranged 8–13 g kg−1, with major contributions from OC (63.2 %), sulfate (20.8 %), and ammonium (14.2 %). Our brick kiln EFPM2.5 values may exceed those previously reported, partly because we sampled emissions at ambient temperature after emission from the stack or kiln allowing some particle-phase OC and sulfate to form from gaseous precursors. The combustion of mixed household garbage under dry conditions had an EFPM2.5 of 7.4 ± 1.2 g kg−1, whereas damp conditions generated the highest EFPM2.5 of all combustion sources in this study, reaching up to 125 ± 23 g kg−1. Garbage burning emissions contained relatively high concentrations of polycyclic aromatic compounds (PAHs), triphenylbenzene, and heavy metals (Cu, Pb, Sb), making these useful markers of this source. A variety of cooking stoves and fires fueled with dung, hardwood, twigs, and/or other biofuels were studied. The use of dung for cooking and heating produced higher EFPM2.5 than other biofuel sources and consistently emitted more PM2.5 and OC than burning hardwood and/or twigs; this trend was consistent across traditional mud stoves, chimney stoves, and 3-stone cooking fires. The comparisons of different cooking stoves and cooking fires revealed the highest PM emissions from 3-stone cooking fires (7.6–73 g kg−1), followed by traditional mud stoves (5.3–19.7 g kg−1), mud stoves with a chimney for exhaust (3.0–6.8 g kg−1), rocket stoves (1.5–7.2 g kg−1), induced-draught stoves (1.2–5.7 g kg−1), and the bhuse chulo stove (3.2 g kg−1), while biogas had no detectable PM emissions. Idling motorcycle emissions were evaluated before and after routine servicing at a local shop, which decreased EFPM2.5 from 8.8 ± 1.3 g kg−1 to 0.71 ± 0.4 g kg−1 when averaged across five motorcycles. Organic species analysis indicated that this reduction in PM2.5 was largely due to a decrease in emission of motor oil, probably from the crankcase. The EF and chemical emissions profiles developed in this study may be used for source apportionment and to update regional emission inventories.


2021 ◽  
Vol 1152 ◽  
pp. 338284
Author(s):  
Sylvain Faixo ◽  
Nicolas Gehin ◽  
Stéphane Balayssac ◽  
Véronique Gilard ◽  
Sofiane Mazeghrane ◽  
...  

2021 ◽  
Vol 55 (4) ◽  
pp. 2234-2242
Author(s):  
Weijun Li ◽  
Lei Liu ◽  
Jian Zhang ◽  
Liang Xu ◽  
Yuanyuan Wang ◽  
...  

2007 ◽  
Vol 121-123 ◽  
pp. 275-278
Author(s):  
Jin Hua Jiang ◽  
Qiu Ming Gao

Cuprous oxide and related materials in nanosizes are of much interest and investigated extensively recently. It is reported here that cubic Cu2O nanocubes were synthesized successfully in aqueous solutions at room temperature in air condition. Copper (II) salts in water were reduced with ascorbate acid in air, using the nonionic pluronic amphiphilic triblock copolymer EO20PO70EO20 (P123) as the template-directing and protecting agent. The average edge length of the cubes varied from 50 to 100 nm. Transmission electron microscopy (TEM) has been used for the shape and structural characterization of the obtained Cu2O nanocubes. The UV-Vis spectra showed an obvious blue-shift (0.53 eV), compared to the band gap of the bulk Cu2O crystal, which makes it a promising candidate in solar energy conversion since this sample can make use of higher energy visible rays of solar spectrum. In the FT-IR spectra the peak of Cu-O bond for the Cu2O is clearly distinguished and several weak peaks of the C-H, C-C and C=O bonds for the organic species can also be detectable, implying a little P123 residua in the products. The effect of the triblock copolymer P123 on the growth of the Cu2O nanocubes is discussed.


1988 ◽  
Vol 20 (11) ◽  
pp. 867-875 ◽  
Author(s):  
Timothy J. Wallington ◽  
Loretta M. Skewes ◽  
Walter O. Siegl ◽  
Ching-Hsong Wu ◽  
Steven M. Japar

2009 ◽  
Vol 60 (11) ◽  
pp. 2759-2766 ◽  
Author(s):  
C. Murphy ◽  
P. Hawes ◽  
D. J. Cooper

The ability of reed beds to remove significant levels of metals from effluent streams is well cited in the literature. Various methods of removal have been postulated and demonstrated including physical methods such as filtration and settlement, precipitation when the metal is present as a salt and adsorption to organic species or take up by macrophytes when the metal is in a soluble or ionic form. Consequently, reed beds have been used in a variety of applications for metal removal in water treatment processes. The distillation process for whisky generates an effluent containing a significant amount of copper which is scoured from the copper stills during the process and cleaning operations. High soluble copper concentrations can breach discharge consents. A horizontal subsurface flow reed bed system has been designed and installed for copper removal at a distillery in Scotland. This paper presents the findings of the literature search, outlines the design of the bed and reviews the performance results.


2018 ◽  
Author(s):  
Jian Wang ◽  
John E. Shilling ◽  
Jiumeng Liu ◽  
Alla Zelenyuk ◽  
David M. Bell ◽  
...  

Abstract. Aerosol particles strongly influence global climate by modifying the properties of clouds. An accurate assessment of the aerosol impact on climate requires knowledge of the concentration of cloud condensation nuclei (CCN), a subset of aerosol particles that can activate and form cloud droplets in the atmosphere. Atmospheric particles typically consist of a myriad of organic species, which frequently dominate the particle composition. As a result, CCN concentration is often a strong function of the hygroscopicity of organics in the particles. Earlier studies showed organic hygroscopicity increases nearly linearly with oxidation level. Such increase of hygroscopicity is conventionally attributed to higher water solubility for more oxidized organics. By systematically varying the water content of activating droplets, we show that for the majority of secondary organic aerosols (SOA), essentially all organics are dissolved at the point of droplet activation. Therefore, the organic hygroscopicity is not limited by solubility, but is dictated mainly by the molecular weight of organic species. Instead of increased water solubility as previously thought, the increase of the organic hygroscopicity with oxidation level is largely because (1) SOA formed from smaller precursor molecules tend to be more oxidized and have lower average molecular weight and (2) during oxidation, fragmentation reactions reduce average organic molecule weight, leading to increased hygroscopicity. A simple model of organic hygroscopicity based on molecular weight, oxidation level, and volatility is developed, and it successfully reproduces the variation of SOA hygroscopicity with oxidation level observed in the laboratory and field studies.


2013 ◽  
Vol 13 (2) ◽  
pp. 1023-1037 ◽  
Author(s):  
C. Mouchel-Vallon ◽  
P. Bräuer ◽  
M. Camredon ◽  
R. Valorso ◽  
S. Madronich ◽  
...  

Abstract. The gas phase oxidation of organic species is a multigenerational process involving a large number of secondary compounds. Most secondary organic species are water-soluble multifunctional oxygenated molecules. The fully explicit chemical mechanism GECKO-A (Generator of Explicit Chemistry and Kinetics of Organics in the Atmosphere) is used to describe the oxidation of organics in the gas phase and their mass transfer to the aqueous phase. The oxidation of three hydrocarbons of atmospheric interest (isoprene, octane and α-pinene) is investigated for various NOx conditions. The simulated oxidative trajectories are examined in a new two dimensional space defined by the mean oxidation state and the solubility. The amount of dissolved organic matter was found to be very low (yield less than 2% on carbon atom basis) under a water content typical of deliquescent aerosols. For cloud water content, 50% (isoprene oxidation) to 70% (octane oxidation) of the carbon atoms are found in the aqueous phase after the removal of the parent hydrocarbons for low NOx conditions. For high NOx conditions, this ratio is only 5% in the isoprene oxidation case, but remains large for α-pinene and octane oxidation cases (40% and 60%, respectively). Although the model does not yet include chemical reactions in the aqueous phase, much of this dissolved organic matter should be processed in cloud drops and modify both oxidation rates and the speciation of organic species.


2001 ◽  
Vol 35 (10) ◽  
pp. 1853-1862 ◽  
Author(s):  
Andreas Limbeck ◽  
Hans Puxbaum ◽  
Luanne Otter ◽  
Mary C. Scholes

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