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Perfluorodecanoic acid

The physical meaning of the g" (ion) potential depends on the accepted model of ionic double layer. The proposed models correspond to the Gouy Chapman diffuse layer, with or without allowance for the Stern modification and/or the penetration of small counterions above the plane of the ionic heads of the adsorbed large ions [17,18]. The presence of adsorbed Langmuir monolayers may induce very high changes of the surface potential of water. For example. A/" shifts attaining ca. —0.9 (hexadecylamine hydrochloride), and ca. -bl.OV (perfluorodecanoic acid) have been observed [68]. [Pg.35]

LOQ not detected, NA not analysed, NR not reported, PFBS perfluorobutanesulfonate, PFDA perfluorodecanoic acid, PFDoDA perfluorododecanoic acid, PFDS perfluorodecanesulfonate, PFHpA perfluoroheptanic acid, PFHxA perfluorohexanoic acid, PFHxS perfluorohexanesulfonate, PFNA perfluorononanoic acid, PFOA perfluorosulfonate acid, PFOS perfluoroctanesulfonate, PFOSA perfluorooctanesulfonamide, PFTDA perfluorotetradecanoic acid, PFUnA perfluoroundecanoic acid, THPFOS lH,lH,2H,2H-perfluoroctanesulfonic acid... [Pg.354]

Adinehzadeh M, Reo NV. 1998. Effects of peroxisome proliferators on rat liver phospholipids Sphingomyelin degradation may be involved in hepatotoxic mechanism of perfluorodecanoic acid. Chem Res Toxicol 11 428-440. [Pg.245]

Chen H, Huang C, Wilson MW, et al. (1994) Effect of the peroxisome proliferators and perfluorodecanoic acid on hepatic cell proliferation and toxicity in Sprague-Dawley rats. Carcinogenesis 15(12) 2847-2850. [Pg.1954]

Chinje, E., Kentish, R, Jamot, B., George, M., and Gibson, G. (1994). Induction of the CYP4A subfamily by perfluorodecanoic acid the rat and the guinea pig as susceptible and non-susceptible species. Toxicol Lett 71, 69-75. [Pg.469]

Myristic acid with carboxyl group ionized (25 A ). Air-water Perfluorodecanoic acid with carboxyl group ionized (25 A ). -501 -9001 -600 -1800... [Pg.50]

PFBS Perfluorobutane sulfonate, PFFIS perfluorohexane sulfonate, PFHxA perfluorohexanoic acid, PFHpA perfluoroheptanoic acid, PFNA perfluorononanoic acid, PFDA perfluorodecanoic acid, and PFUnDA perfluoroundecanoic acid, PFUnDA perfluoroundecanoate, PFDA perfluorodecanoate, PFHpA perfluoro-heptanoate and PFHxA, PFTeDA perfluorotetradecanoate, PFOS, PFNA, PFOA... [Pg.133]

PFOA, Fig. 7.1) has been the most commonly used, but chain lengths of C9 (perfluorononanoic acid— PFNA), CIO (perfluorodecanoic acid—PFDA), and longer have also been utihzed. Although PFCAs can be produced in separate chain lengths, most commercial products consist of mixtures of several chain lengths. [Pg.179]

Kato K, Wong LY, Jia LT et al (2011) Trends in exposure to polyfluoroalkyl chemicals in the US population 1999-2008. Environ Sci Teehnol 45(19) 8037-8045 Kawashima Y, Kobayashi H, Miura H et al (1995) Characterization of hepatic responses of rat to administration of perfluorooctanoic and perfluorodecanoic acids at low-levels. Toxicology 99(3) 169-178... [Pg.198]

Nelson DL, Frazier DE, Ericson JE et al (1992) The effects of perfluorodecanoic acid (PFDA) on humoral, cellular, and innate immunity in Fischer 344 rats. Immunopharm Immunotoxicol 14(4) 925-938... [Pg.199]

Fujiwara, Y Amao, Y. Novel optical oxygen sensing material 1-pyrenedecanoic acid and perfluorodecanoic acid chemisorbed onto anodic oxidized aluminium plate. Sens. Actuators, B Chem. 2004, B99,130-133. [Pg.341]

Fig. 3.6 Potentiometric titration curves of perfluorodecanoic acid (C9F19COOH) (O) and nitric acid (HNO3) ( ). Glass electrode and Ag/AgCI reference electrode at 25°C. (From Ref. 21. Reproduced by permission of Steinkopff.)... Fig. 3.6 Potentiometric titration curves of perfluorodecanoic acid (C9F19COOH) (O) and nitric acid (HNO3) ( ). Glass electrode and Ag/AgCI reference electrode at 25°C. (From Ref. 21. Reproduced by permission of Steinkopff.)...
The solubility of fluorinated surfactants depends on the hydrophile of the surfactant, in addition to the structure of the fluorinated group. The solubility of perfluoroalkanoic acids in water, like the solubility of nonfluorinated alkanoic acids, decreases with increasing chain length. At 25°C, perfluorohexanoic acid and shorter-chain perfluoroalkanoic acids are miscible with water in all proportions. However, perfluorooctanoic acid and perfluorodecanoic acid are only slightly soluble in water [4]. [Pg.198]

Perfluorodecanoic acid (PDA) forms solid 1 1 complexes with cationic copolymers, poly(diallyldimethylammonium chloride)-co-(Ar-methyl-iV-vinylac-etamide) [144]. The mesomorphic structure of the complexes consist of two-dimensional ordered columnar stacks of disklike aggregates. These long-chain complexes of low surface energy are of practical interest for the development of high-performance coatings. [Pg.328]

Fig. 9.6 The 200-1800-cm Raman spectra of perfluorodecanoic acid (a) and its lithium (b), sodium (c), and ammonium (d) salts at 22°C. (From Ref. 72. Reproduced by permission of Academic Press, Inc.)... Fig. 9.6 The 200-1800-cm Raman spectra of perfluorodecanoic acid (a) and its lithium (b), sodium (c), and ammonium (d) salts at 22°C. (From Ref. 72. Reproduced by permission of Academic Press, Inc.)...
See other pages where Perfluorodecanoic acid is mentioned: [Pg.735]    [Pg.312]    [Pg.184]    [Pg.735]    [Pg.72]    [Pg.1084]    [Pg.1830]    [Pg.1946]    [Pg.456]    [Pg.156]    [Pg.51]    [Pg.365]    [Pg.327]    [Pg.64]    [Pg.6109]    [Pg.268]    [Pg.183]    [Pg.195]    [Pg.88]    [Pg.354]   
See also in sourсe #XX -- [ Pg.42 ]

See also in sourсe #XX -- [ Pg.50 ]



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Perfluorodecanoic

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