2010
DOI: 10.1016/j.tsf.2010.07.052
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Based on atom transfer radical polymerization method preparation of fluoropolymer superhydrophobic films

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Cited by 17 publications
(12 citation statements)
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“…15 Poly(dimethylsiloxane) and uoropolymers are advantageous for generating superhydrophobic surfaces alone or in combination with other polymers as well as inorganic nanoparticles. [16][17][18] For example, superhydrophobic surfaces can be fabricated by casting a micelle solution of polystyrene-bpoly(hexauorobutyl-methacrylate) in 1,1,2-trichlorotriuoroethane onto a glass substrate. 16 However, most of the methods for preparation of superhydrophobic surfaces cannot be easily scaled up because of the very strict preparation conditions, complicated preparation processes, time consuming nature and high cost.…”
mentioning
confidence: 99%
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“…15 Poly(dimethylsiloxane) and uoropolymers are advantageous for generating superhydrophobic surfaces alone or in combination with other polymers as well as inorganic nanoparticles. [16][17][18] For example, superhydrophobic surfaces can be fabricated by casting a micelle solution of polystyrene-bpoly(hexauorobutyl-methacrylate) in 1,1,2-trichlorotriuoroethane onto a glass substrate. 16 However, most of the methods for preparation of superhydrophobic surfaces cannot be easily scaled up because of the very strict preparation conditions, complicated preparation processes, time consuming nature and high cost.…”
mentioning
confidence: 99%
“…[16][17][18] For example, superhydrophobic surfaces can be fabricated by casting a micelle solution of polystyrene-bpoly(hexauorobutyl-methacrylate) in 1,1,2-trichlorotriuoroethane onto a glass substrate. 16 However, most of the methods for preparation of superhydrophobic surfaces cannot be easily scaled up because of the very strict preparation conditions, complicated preparation processes, time consuming nature and high cost. As a result, applications of such superhydrophobic surfaces have been limited in practice.…”
mentioning
confidence: 99%
“…However, it is an active metal that does not resist corrosion enough, especially in the presence of chloride anions [ 110 ]. Therefore, several of the solutions were tested to protect copper and its alloys from corrosion [ 10 , 111 , 112 ]. In this regard, triazole derivatives such as benzotriazole (BTA) are the first 1 H -1,2,3-triazole compounds investigated as corrosion inhibitors for copper and its alloys and so they are classified as effective corrosion inhibitors for copper surfaces [ 113 , 114 , 115 , 116 ].…”
Section: 123-triazoles As Corrosion Inhibitorsmentioning
confidence: 99%
“…Such materials are of interest because of their use in creating antibiotic resistance materials, their non-linear optical properties, and use as rheological modifiers by patterning surfaces on the nanometre scale. Wei et al 10 also synthesized a polystyrene-blockpoly(2,2,3,4,4,4-hexafluorobutyl-methacrylate) (St-b-HFMA) diblock copolymer by ATRP. This material was then dissolved in the solvent 1,1,2-trichlorotrifluoroethane (Freon 113) forming a micellar solution.…”
Section: Introductionmentioning
confidence: 99%