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H perfluorooctyl silane

Manufactured by Merck Group
Sourced in United Kingdom

(3-Perfluorooctyl)silane is a fluorinated silane compound used in various laboratory applications. It serves as a silylating agent, which can modify the surface properties of materials. The compound is often utilized in the preparation of coatings, monolayers, and for surface functionalization in research and development settings. Its core function is to provide a fluorinated layer on target surfaces.

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3 protocols using h perfluorooctyl silane

1

Fabrication of SU8 Microfluidic Devices

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3″ silicon test wafers (University Wafer, Catalog #447, Boston, MA) were rinsed extensively with acetone and isopropyl alcohol, then placed on a hotplate at 300 °C for a minimum of two hours to drive off water. Wafers were then coated with SU8 2025 photoresist (MicroChem Corp., Westborough, MA) and spun on a WS-400-6NPP spin coater (Laurell Technologies Corporation, North Wales, PA) using empirical protocols. After soft bake, photoresist was exposed on a Karl Suss MJB3 mask aligner (Suss MicroTec, Garching bei München, Deutschland) using transparency masks (printed by CAD/Art Services, Bandon, OR) mounted on a quartz slide (Chemglass Life Sciences, Vineland, NJ). Wafers were then post-exposure baked according to MicroChem protocol and developed using SU8 Developer (MicroChem). The thickness of resultant channel masks was confirmed at multiple locations using a NewView 7300 optical profilometer (Zygo Corp., Middlefield, CT), and re-verified after device assembly with fluorescence imaging. To facilitate later release of molded devices, wafers were treated with 1% v/v Trichloro(1 H,1 H,2 H,2H-perfluorooctyl)silane (Sigma-Aldrich Corp., St. Louis, MO) in hexanes for 5–30 minutes, dependent on ambient humidity, at room temperature and washed extensively with isopropyl alcohol before overnight hard bake at 80 °C in a hybridization oven.
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2

Fabrication of Polymeric Microfluidic Devices

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Poly(dimethylsiloxane) (Sylgard® 184) was purchased from Dow Corning Corporation (Michigan, USA), and poly(methyl methacrylate) from theplasticshop.co.UK (Coventry, UK). Epoxy adhesive (Yellow Dual Cartridge) was purchased from RS Components Ltd. (Corby, UK). Poly(lactic-co-glycolic acid), Pluronic® F127, dichloromethane, polyoxyethylene (40) stearate, trichloro-(1 H, 1 H, 2 H, 2 H-perfluorooctyl)-silane, and Evans blue dye were purchased from Sigma Aldrich (Gillingham, UK). Phosphate buffered saline was purchased from Life Technologies (Thermo Fisher Scientific Inc., Massachusetts, USA) and 1,2-distearoyl-sn-glycero-3-phosphocholine from Avanti Polar Lipids (Alabama, USA). Perfluorohexane was purchased from Apollo Scientific Ltd. (Stockport, UK). Nitrogen (N2) gas was provided by The BOC Group plc (Guildford, UK).
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3

Fabrication of Porous PDMS Haircells

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The porous PDMS layer with haircell structures was fabricated by a well-known polymer molding technique. In order to facile demold the porous PDMS layer with haircell structures from the mold, trichloro(1H,1H,2H,2H-perfluorooctyl)silane (Sigma Aldrich) was vaporized on the mold under vacuum condition for 50 min. Subsequently, the PDMS with crystallized citric acid powders and a curing agent were mixed in a weight ratio of 15 : 1 and spin-coated on the silane treated mold for the thickness of 40 μm, followed by solidification at 100 °C for 1 h. The citric acid powder in PDMS was dissolved in ethanol for 1 min 30 s to form the porous PDMS layer with haircell structures on the mold.
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