2015
DOI: 10.1016/j.chemosphere.2014.08.039
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Selected physicochemical aspects of poly- and perfluoroalkylated substances relevant to performance, environment and sustainability—Part one

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Cited by 225 publications
(131 citation statements)
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“…Common examples of PFAAs include perfluorooctanoic acid (PFOA) and perfluorohexanoic acid (PFHxA), perfluorooctane sulfonic acid (PFOS) and perfluorohexane sulfonic acid (PFHxS). These terminal end products are extremely stable once released to the environment, and are the primary driver of PFAS risk concerns at present (Krafft and Riess, 2015). However, nearly all other PFASs can be considered precursors to PFAAs, and these precursors can include the fluorotelomer alcohols (FTOHs) and mono- and di-substituted polyfluoroalkyl phosphates (monoPAPs, diPAPs).…”
Section: Introductionmentioning
confidence: 99%
“…Common examples of PFAAs include perfluorooctanoic acid (PFOA) and perfluorohexanoic acid (PFHxA), perfluorooctane sulfonic acid (PFOS) and perfluorohexane sulfonic acid (PFHxS). These terminal end products are extremely stable once released to the environment, and are the primary driver of PFAS risk concerns at present (Krafft and Riess, 2015). However, nearly all other PFASs can be considered precursors to PFAAs, and these precursors can include the fluorotelomer alcohols (FTOHs) and mono- and di-substituted polyfluoroalkyl phosphates (monoPAPs, diPAPs).…”
Section: Introductionmentioning
confidence: 99%
“…The high Hansch parameter (p R = 1.44) [3] of the CF 3 Sg roup affords ah igh lipophilicity to trifluoromethylthiolated molecules, thereby contributing to the better transmembrane permeability of CF 3 S-substituted molecules and, consequently,their improved bioavailability. [4] Besides trifluoromethylated substituents, higher perfluorinated groups can also be characterized by interesting properties that are useful for variousa pplications, [5] as demonstrated by Fulvestrant with regard to an estrogen receptor antagonist used in the treatment of hormone receptor-positive metastatic breast cancer. [6] Consequently,the synthesis of perfluoroalkylthiolated compounds couldb eofs ome interest.…”
Section: Introductionmentioning
confidence: 99%
“…They are widely used in various industrial and consumer applications, mainly thanks to their unique ability to repel both water and oil. As a consequence, these compounds show a global distribution all over the world and have been detected not only in environment samples [16,17] but also in human blood [18,19]. It show persistence in the environment [20] and some of them are related to different carcinogenic actions [21].…”
Section: Introductionmentioning
confidence: 99%