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The concentration of oxygenated polynuclear aromatic hydrocarbons (oxy-PAH) and nitrated PAH (nitro-PAH) identified in the moderately polar particulate fractions are given.
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This dynamic dilution sampling system was employed to minimize the potential loss of polar organic and particulate species during the sampling of the hot syngas.
The moderately polar chemical fraction of the particulates contained more than 50% of the direct acting Ames assay mutagenicity for the total extract.
By setting functionalization conditions to favor hydrophilic surface properties, the treated ash can readily be dispersed in a polar solvent such as water: larger particulates then settle out of suspension, while the lighter nanoparticles remain in the supernatant and are ready for use.
The gas and particulate phase material was fractionated by HPLC into nonpolar, moderately polar and highly polar chemical fractions.
In contrast, proteins and particulate material with a majority of non-polar surface residues may remain in solution even at the higher salt concentration.
While polar organic chemicals can also sorb by other mechanisms, e.g., ion exchange, the low particulate levels observed preclude the likelihood that sorption to such is a major attenuation process, at least in this system.
For example, a solvent mixture combining polar and non-polar solvents was reported to increase PAH recoveries from soot, sediment and Standard Reference Material SRMM) diesel particulate matter [26, 27].
However, several papers reported advantages of using a mixture of polar and non-polar solvents for gaining higher recoveries of PAHs from complex matrices such as soot and diesel particulate matter [26, 27].
Important gaps in our knowledge of exposure measurements are identified, e.g., particulates (including polyaromatic hydrocarbons); 1,3-butadiene, asbestos, chromium, cadmium, arsenic, vinyl chloride, methylene chloride, and most polar organics.
Particulate sand for glass.
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