Contact Angle, Wettability and Adhesion, Volume 6
DOI: 10.1163/ej.9789004169326.i-400.77
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A Novel Design Of Water- And Oil-Repellent Surface Modifier Having Double-Fluoroalkyl Groups

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Cited by 4 publications
(5 citation statements)
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“…3, Γ CMC values were determined, and are listed in Table 3. With respect to the occupied minimum area A G , the values for the 1 1 type F4C10 was 0.43 nm 2 , which was consistent with the values obtained from π-A measurements of various semifluoroalkanoic acids on water 28 . However, the A G values of the 1) Values at the 1st break point.…”
Section: Surface Tension Measurementssupporting
confidence: 87%
“…3, Γ CMC values were determined, and are listed in Table 3. With respect to the occupied minimum area A G , the values for the 1 1 type F4C10 was 0.43 nm 2 , which was consistent with the values obtained from π-A measurements of various semifluoroalkanoic acids on water 28 . However, the A G values of the 1) Values at the 1st break point.…”
Section: Surface Tension Measurementssupporting
confidence: 87%
“…3, Γ cmc values of 11a-c and 12a were determined using 4 5 points just below cmc and listed in Table 9. With respect to the occupied minimum area A, the values for 1 1 type 11a-c were 0.36 nm 2 C 4 F 9 to 0.4 nm 2 C 8 F 17 , which was consistent with the values obtained from π-A measurements of semifl uoroalkanoic acid on water 26 . The A value of 12a 0.70 nm 2 was smaller than twice the A values of 1 1 type 11a-c, which would indicate that two hydrophobic chains of Gemini 12a can align more close at the air/ water interface than monomeric surfactant.…”
Section: Surface Tension Measurementssupporting
confidence: 87%
“…The value of ν used in this study was 2, because the concentration of TBAH was not high and the volume of tetrabutylammonium counter ions adsorbed at the air/water interface would be large. In our previous work 20 , A G values for Rf-CH 2 n -COOK Rf C 4 F 9 , C 6 F 13 , C 8 F 17 ; n 3-10 were in the range 0.35-0.45 nm 2 per molecule. Contrary to our expectations, all the A G values for 15 were twice as large as those for Rf-CH 2 n -COOK; this may be because of the large volume of tetrabutylammonium counter ions at the air/water interface.…”
Section: 1 Lactone Surfactantsmentioning
confidence: 79%
“…The residue was treated in a similar manner to that described above. The residue was recrystallized from diethyl ether to give 1 s 2 2.36 g, yield 20 . Dimethyl 1,1-cyclopropanedicarboxylate was obtained from the filtrate in 60 yield.…”
Section: Synthesismentioning
confidence: 99%
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