The spreading behaviour of defined trisiloxane surfactants of general formula [(CH 3 ) 3 SiO] 2 CH 3 Si(CH 2 ) 3 (OCH 2 CH 2 ) n OCH 3 (n = 3-9) on five different solid surfaces has been investigated. Maximum spreading areas and rates are found on non-polar or slightly polar surfaces of 30 to 40 mN
Silicon-modified surfactants and wetting: III. The spreading behaviour of equimolar mixtures of nonionic trisiloxane surfactants on a low-energy solid surface
β Scribed by R. Wagner; Y. Wu; H. v. Berlepsch; F. Rexin; T. Rexin; L. Perepelittchenko
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 139 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0268-2605
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β¦ Synopsis
The spreading behaviour of binary and ternary equimolar mixtures of siloxane surfactants of general formula [(CH 3 ) 3 SiO] 2 CH 3 Si(CH 2 ) 3 (OCH 2 CH 2 ) n OCH 3 , n = 3-9, has been investigated. The mixtures show a pronounced temperature dependence on the initial spreading rate. Mixtures imitating the average oligoethylene glycol chain length n = 5 are the fastest spreaders at 15 Β°C. At 23 Β°C and 40 Β°C these mixtures spread fastest sucking n = 6 and n = 8, respectively. For a given average chain length an increasing length difference between the components of the binary mixtures reduces the initial spreading rate. Nevertheless, substantial differences between the phase transition temperature T c from the lamellar phase (L a ) into the twophase state (2Ξ¦) and the actual spreading temperature are tolerated. A clear relation between phase transition temperature T c and initial spreading rate does not exist.
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The siloxanyl-modified carbohydrate surfactants investigated consist of the four structural elements: (1) siloxanyl moiety; (2) spacer; (3) carbohydrate unit; and (4) modifying element. By static surface tension (β₯ lv , ) and wetting tension (β₯ sv Οͺ β₯ sl , β£) measurements the contact angles of aqueo
Defined surfactants of general formula [(CH 3 ) 3 SiO] 2 CH 3 Si(CH 2 ) 3 (OCH 2 CH 2 ) 3-9 OCH 3 , have been synthesized from the corresponding oligoethylene glycol monoallyl monomethyl ethers via hydrosilylation. The concentrationdependent spreading performance on hydrophobized silicon wafers has
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