Rapid determination of polycyclic aromatic hydrocarbons (PAH) in yeasts grown on n-paraffins and molasses

Santoro, A.; Modica, Rossana; Paglialunga, S.; Bartošek, I.

doi:10.1016/0378-4274(79)90091-2

Cited by 5 publications

(1 citation statement)

References 9 publications

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“…There are several hundred different PAHs combinations, wherein up to 28 compounds have been identified as hazardous contaminants in January 2008 by the U.S. Environmental Protection Agency. For a long time, PAHs treatment has been one of the hottest issues in scientific research. − …”

Section: Introductionmentioning

confidence: 99%

Adsorption of Polycyclic Aromatic Hydrocarbons (Fluoranthene and Anthracenemethanol) by Functional Graphene Oxide and Removal by pH and Temperature-Sensitive Coagulation

Zhang

Cai

et al. 2013

ACS Appl. Mater. Interfaces

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A new kind of functional graphene oxide with fine stability in water was fabricated by mixing graphene oxide (GO) and brilliant blue (BB) with a certain weight ratio. The adsorption performance of this mixture of BB and GO (BBGO) to polycyclic aromatic hydrocarbons (anthracenemethanol (AC) and fluoranthene (FL)) was investigated, and the results indicated BBGO possessed adsorption capacity of 1.676 mmol/g and removal efficiency of 72.7% as to AC and adsorption capacity of 2.212 mmol/g and removal efficiency of 93.2% as to FL. After adsorption, pH and temperature-sensitive coagulation (PTC) method was used to remove the AC/BBGO or FL/BBGO complex and proved to be an effective approach to flocculate the AC/BBGO or FL/BBGO complex into large flocs, which tended to be removed from the aqueous solution.

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Section: Introductionmentioning

confidence: 99%

Adsorption of Polycyclic Aromatic Hydrocarbons (Fluoranthene and Anthracenemethanol) by Functional Graphene Oxide and Removal by pH and Temperature-Sensitive Coagulation

Zhang

Cai

et al. 2013

ACS Appl. Mater. Interfaces

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Uptake, translocation and metabolism of anthracene in bush bean (Phaseolus Vulgaris L.)

Edwards

1986

Enviro Toxic and Chemistry

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The roots of bush bean (Phaseolus vulgaris L.) plants growing in nutrient solution were exposed to [side ring‐U‐14C]anthracene (0.01 mg L−1 solution) during flowering and seed production. At harvest, 60% of the total 14C dose was in the roots, 3% in the stems, 3% in the leaves, 0.1% in the pods, 17% in the nutrient solution and 16% unaccounted for. More than 90% of the anthracene (75 mg/plant) was metabolized over the 30‐d exposure period. The results suggest that most of the metabolism occurred in the plant tissues. At harvest, 8.7% of the anthracene dose was found (unmetabolized) in the roots, 1.5% in the nutrient solution, 0.53% in the stems and 0.03% in the leaves. Quantities of the parent compound were too small to detect in the pods and seeds. The remainder of the [14C]anthracene taken up by the plants was metabolized to polar metabolites (29%) and nonpolar metabolites (18%) or structurally incorporated into compounds that were not extracted (44%).

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Comparative kinetics of oral benz(a)anthracene, chrysene and triphenylene in rats: Study with hydrocarbon mixtures

et al. 1984

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Rapid determination of polycyclic aromatic hydrocarbons (PAH) in yeasts grown on n-paraffins and molasses

Cited by 5 publications

References 9 publications

Adsorption of Polycyclic Aromatic Hydrocarbons (Fluoranthene and Anthracenemethanol) by Functional Graphene Oxide and Removal by pH and Temperature-Sensitive Coagulation

Adsorption of Polycyclic Aromatic Hydrocarbons (Fluoranthene and Anthracenemethanol) by Functional Graphene Oxide and Removal by pH and Temperature-Sensitive Coagulation

Uptake, translocation and metabolism of anthracene in bush bean (Phaseolus Vulgaris L.)

Comparative kinetics of oral benz(a)anthracene, chrysene and triphenylene in rats: Study with hydrocarbon mixtures

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