2015
DOI: 10.1016/j.chroma.2015.04.035
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A critical evaluation of an asymmetrical flow field-flow fractionation system for colloidal size characterization of natural organic matter

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Cited by 46 publications
(35 citation statements)
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References 51 publications
(69 reference statements)
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“…Molecular size spectra of bulk soil‐DOM samples were characterized using a flow field‐flow fractionation (FlFFF) system (AF2000, Postnova) coupled online with a UV absorbance detector (Postnova SPD20A, set at 254 and 355 nm) and two fluorescence detectors (Shimadzu RF20A), with Ex/Em at 275/340 nm and 350/450 nm (Zhou & Guo, ). The coupling of FlFFF with online detectors allowed a continuous size separation and characterization of chromophoric, protein‐like, and humic‐like DOM components at the same time (Stolpe et al, ).…”
Section: Methodsmentioning
confidence: 99%
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“…Molecular size spectra of bulk soil‐DOM samples were characterized using a flow field‐flow fractionation (FlFFF) system (AF2000, Postnova) coupled online with a UV absorbance detector (Postnova SPD20A, set at 254 and 355 nm) and two fluorescence detectors (Shimadzu RF20A), with Ex/Em at 275/340 nm and 350/450 nm (Zhou & Guo, ). The coupling of FlFFF with online detectors allowed a continuous size separation and characterization of chromophoric, protein‐like, and humic‐like DOM components at the same time (Stolpe et al, ).…”
Section: Methodsmentioning
confidence: 99%
“…A polythersulfone ultrafiltration membrane with a NMWCO (nominal molecular weight cutoff) of 0.3 kDa (manufacturer‐rated) was used along with the FlFFF system. However, the apparent pore size or NMWCO of this 0.3 kDa membrane (manufacturer‐rated) was ~1.9 kDa (Zhou & Guo, ), based on a 90% recovery rate for a series of polystyrene sulfonate standards by the FlFFF system under the specific operational conditions (Table S1). Therefore, the molecular size spectra reported here were those of DOM >1.9 kDa.…”
Section: Methodsmentioning
confidence: 99%
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“…Despite it being widely recognized that NOM is a sink for a range of pollutants, including metals and organics, and thus influences their bioavailability, interactions with NOM are not considered as part of standard toxicity testing, nor indeed in modeling of pollutant fate and behavior. This becomes especially problematic for NMs, where their enormous surface area, and sizes similar to those of NOM complexes in aquatic systems (size partitioning of dissolved NOM samples using asymmetrical flow field flow fractionation has shown a predominant size in the <5 nm size range), means that it is no longer a question of NOM removing the pollutants from solution, but rather that the NOM binds to the surface of the NMs forming NM‐NOM complexes, or a NOM‐corona, thereby altering the NM surface properties and subsequent interactions. Other constituents of the aquatic environment, including exopolysaccharides secreted by bacteria and biofilms, and proteins and other biomolecules secreted and excreted by aquatic organisms, will also compete with NOM, depending on their affinities for the NM surface.…”
Section: Introductionmentioning
confidence: 99%
“…The recovery of the optimised method was calculated by injecting 20 µl of the sample with the cross-flow set to zero and calculating the area under the curve of the UV-Vis (Geiss et al 2013; Zhou & Guo 2015). Next, another 20 µl of the same sample were injected under the optimised conditions, in which the sum of the area of the void peak and the main peak (together with the corresponding release peak, which elutes after minute 65 when the CF is stopped) were estimated in the UV-Vis and the recovery was calculated by dividing the areas of interest: …”
Section: Resultsmentioning
confidence: 99%