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1.
Bioresour Technol ; 408: 131157, 2024 Sep.
Article de Anglais | MEDLINE | ID: mdl-39059588

RÉSUMÉ

The present study successfully synthesized a novel biochar adsorbent (M-L-BC) using litchi seed modified with zinc chloride for PFASs removal in water. M-L-BC greatly enhanced removal of all examined PFASs (>95 %) as compared to the pristine biochar (<40 %). The maximum adsorption capacity was observed for PFOS, reaching 29.6 mg/g. Adsorption kinetics of PFASs followed the pseudo-second-order model (PSO), suggesting the predominance of chemical adsorption. Moreover, characterization and density functional theory (DFT) calculations jointly revealed involvement of surface complexation, electrostatic interactions, hydrogen bonding, and hydrophobic interactions in PFAS adsorption. Robust PFAS removal was demonstrated for M-L-BC across a wide range of pH (3-9), and coexisting ions had limited impact on adsorption of PFASs except PFBA. Furthermore, M-L-BC showed excellent performance in real water samples and retained reusability after five cycles of regeneration. Overall, M-L-BC represents a promising and high-quality adsorbent for efficient and sustainable removal of PFASs from water.


Sujet(s)
Charbon de bois , Chlorures , Litchi , Graines , Polluants chimiques de l'eau , Purification de l'eau , Composés du zinc , Charbon de bois/composition chimique , Adsorption , Polluants chimiques de l'eau/isolement et purification , Graines/composition chimique , Purification de l'eau/méthodes , Chlorures/composition chimique , Composés du zinc/composition chimique , Litchi/composition chimique , Cinétique , Concentration en ions d'hydrogène , Fluorocarbones/composition chimique , Eau/composition chimique
2.
Mar Pollut Bull ; 203: 116444, 2024 Jun.
Article de Anglais | MEDLINE | ID: mdl-38705002

RÉSUMÉ

An efficient and sensitivity approach, which combines solid-phase extraction or ultrasonic extraction for pretreatment, followed by ultra-performance liquid chromatography-tandem mass spectrometry, has been established to simultaneously determine eight lipophilic phycotoxins and one hydrophilic phycotoxin in seawater, sediment and biota samples. The recoveries and matrix effects of target analytes were in the range of 61.6-117.3 %, 55.7-121.3 %, 57.5-139.9 % and 82.6 %-95.0 %, 85.8-106.8 %, 80.7 %-103.3 % in seawater, sediment, and biota samples, respectively. This established method revealed that seven, six and six phycotoxins were respectively detected in the Beibu Gulf, with concentrations ranging from 0.14 ng/L (okadaic acid, OA) to 26.83 ng/L (domoic acid, DA) in seawater, 0.04 ng/g (gymnodimine-A, GYM-A) to 2.75 ng/g (DA) in sediment and 0.01 ng/g (GYM-A) to 2.64 ng/g (domoic acid) in biota samples. These results suggest that the presented method is applicable for the simultaneous determination of trace marine lipophilic and hydrophilic phycotoxins in real samples.


Sujet(s)
Biote , Surveillance de l'environnement , Toxines de la flore et de la faune marines , Eau de mer , Extraction en phase solide , Toxines de la flore et de la faune marines/analyse , Surveillance de l'environnement/méthodes , Eau de mer/composition chimique , Sédiments géologiques/composition chimique , Polluants chimiques de l'eau/analyse , Spectrométrie de masse en tandem , Interactions hydrophobes et hydrophiles , Acide kaïnique/analogues et dérivés , Acide kaïnique/analyse , Composés hétérocycliques 3 noyaux , Hydrocarbures cycliques , Imines
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