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Solef 6010

Manufactured by Solvay
Sourced in Italy

Solef 6010 is a polyvinylidene fluoride (PVDF) resin designed for laboratory equipment. It offers high chemical resistance and thermal stability. The material can be used for the fabrication of various laboratory components and devices.

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10 protocols using solef 6010

1

PVDF Membrane Fabrication with Additives

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Solef 6010 and Solef 6020 (SOLVAY, Brussels, Belgium) were used as PVDF resins for the M-1 [16 ,17 ] and M-3 membrane fabrications [18 (link)], respectively. AEROSIL-R972 (NIPPON AEROSIL, Tokyo, Japan) was used as the hydrophobic silica which is a pore-forming agent. Di (2-ethylhexyl) phthalate (DOP), dibutyl phthalate (DBP) and glycerol triacetate (GTA) were used as diluents of the PVDF polymer. Diethyl phthalate (DEP) was used as an extruded solvent in a thermally induced phase separation (TIPS) process. CH2Cl2, EtOH, and NaOH were used to wash the membrane after fabrication. 1-Buthanol was used to measure membrane porosity. NaCl was used as a model electrolyte in the feed solution. All these chemicals were purchased from FUJIFILM Wako Pure Chemical Corporation, Osaka, Japan. A fluoropolymer FS-392B (Fluoro Technology Co. Ltd., Aichi, Japan) was used as the hydrophobic agent.
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2

Preparation of PVDF Polymer Composite

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Microcrystalline cellulose (310697-500G), sulphuric acid, and dimethylformamide (DMF) were obtained from Sigma Aldrich, while poly (vinylidene fluoride) (PVDF) with a molecular weight of Mw = 300 kg·mol-1 was purchased from Solvay (Brussels, Belgium) under the name of Solef® 6010.
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3

PVDF Membrane Fabrication via Solvent Casting

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PVDF (Solef® 6010; Mw = 322 kg/mol) was kindly supplied by Solvay Specialty Polymers (Bollate, Italy). TEP (Sigma Aldrich, Milan, Italy) was used as a solvent without further purification. Polyvinylpyrrolidone (PVP K17, BASF, Ludwigshafen, Germany, Mw = ~9 kg/mol) and PEG (PEG-200, Sigma Aldrich, Milan, Italy, Mw = 200 g/mol) were selected as pore former additives. PVP was desiccated under vacuum at 50 °C for 12 h before use. Bi-distilled water at 15 °C was used as coagulation medium.
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4

Fluorescent Polymer Coatings for Luminescent Solar Concentrators

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All materials employed in this study are of commercial source and were used as received. Lumogen F Red 305 (from now on referred to as LR305, BASF) was used as the fluorescent doping species in all polymeric coatings presented in this work. PMMA (Perspex XT, Lucite) was used as polymeric carrier in reference luminescent coatings. Solef 6010 poly(vinylidenefluoride) – PVDF, Solef 31508 (a poly(vinylidenefluoride-co-chlorotrifluoroethylene) copolymer), and Solef 11005 (a poly(vinylidenefluoride-co-hexafluoropropylene-co-hydroxyethylacrylate) terpolymer) were produced and supplied by Solvay Specialty Polymers. Chloroform (CHCl3), toluene and N-methylpyrrolidone (NMP) were purchased by Sigma Aldrich and used as solvents for the fabrication of LSC devices.
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5

PVDF Hollow Fiber Membrane Fabrication

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PVDF HF membranes were prepared by the dry/wet spinning technique described elsewhere [25 (link),26 (link),27 (link)]. The polymeric dope was prepared by dissolving poly(vinylidene fluoride) Solef® 6010 (kindly provided by Solvay Advanced Polymers, Bollate, Italy) 25 wt.% in dimethyl formamide (DMF) (Carlo Erba Reagenti, Italy). Poly-vinyl pyrrolidone Luviskol K-17 (PVP K-17, Mw = 12 kg/mol) was purchased from BASF and used as pore forming additive, in concentration of 35 wt.%. PVP was desiccated at 50 °C under vacuum overnight before use. Different fibers types were produced by varying the bore fluid composition and flow rate. All the other spinning parameters were kept constant. The detailed conditions of fiber spinning are resumed in Table 1.
The produced PVDF hollow fibers were kept in frequently refreshed water bath for one day, to remove residual solvent and ensure complete coagulation. Afterwards, they were treated with sodium hypochlorite 4000 ppm, buffered to pH 7, in order to leach out PVP from membrane pores and increase permeability. Fibers were soaked in a glycerol/water solution (30 wt.%), in order to avoid collapse of their porous structure, before the final drying.
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6

PVDF-based Polymer Solution Preparation

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Polyvinylidenefluoride (PVDF) was Solef®6010 supplied by Solvay Specialty Polymers (Milan, Italy). It is a white powder with a density of 1.78 gr/m3 and a melting temperature point between 165 and 177 °C. PVDF was chosen because it is an inert material suitable for use in contact with food products. Dimethylformammide (DMF), supplied by Sigma Aldrich (Milan, Italy), was used as a solvent for the solution. Polyvinilpyrrolidone (PVP, Luviskol K17, MW = 12 kg/mol) was supplied by BASF (Ludwigshafen, Germany). Glycerol was supplied by Carlo Erba Reagents (Milan, Italy).
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7

Polymer Electrolyte Membrane Fabrication

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Commercial PVDF (Solef® 6010) was sourced from Solvay Specialty Polymers (Bollate, Italy). POEM (Mw = 500), copper(I) chloride (CuCl), dimethylacetamide (DMAc) and methyl ethyl ketone (MEK) were purchased from Sigma-Aldrich. N-methyl-2-pyrrolidone (NMP greater than 99.5) was obtained from Duksan and 4,40-dimethyl-2,20-dipyridyl (DMDP) was purchased from Thermo Fisher Scientific.
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8

PVDF Membrane Fabrication and Characterization

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Solef 6010 (SOLVAY, Brussels, Belgium) was used as the PVDF resin [18 (link),24 ]. AEROSIL-R972 (NIPPON AEROSIL, Tokyo, Japan) was the hydrophobic silica, and functioned as a pore-forming agent. The PVDF polymer was diluted using Di (2-ethylhexyl) phthalate (DOP) and dibutyl phthalate (DBP). Following fabrication, CH2Cl2, EtOH and NaOH were used to wash the membrane. The membrane porosity was determined using 1-Butanol., NaCl was used as a model electrolyte in the feed solution. Sodium dodecyl sulfate (SDS) was used as a model surface-active solute. All of these chemicals were purchased from FUJIFILM Wako Pure Chemical Corporation, Osaka, Japan. The fluoropolymer FS-392B (Fluoro Technology Co. Ltd., Aichi, Japan), was used as the hydrophobic agent [25 ,26 ].
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9

PVDF Membrane Fabrication Protocol

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PVDF powders Solef 6010, Solef 1015, and Solef 6020 were kindly donated by Solvay Specialty Polymers (Bollate, Italy). N-methyl-2-pyrrolidone (NMP, 99%) was provided by Panreac (Inca, Spain). Non-woven Hollytex 34 GR was provided by STEM Company (Teijin Aramid, Arnhem, The Netherlands). Distilled water was used as a non-solvent in the coagulation bath.
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10

Preparation of SiO2 Nanoparticle Composite

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SiO2 nanoparticles
with a particle size of 30 nm were obtained from Shanghai Aladdin
Co. Ltd. PVDF powders (Solef 6010) were purchased from Solvay Co.
(Germany). N-Methyl-2-pyrrolidone (NMP, AR) and 1
mol/L LiPF6 (in EC/DEC = 1:1 vol/vol) were bought from
Suzhou Doduo Chemical Technology Co. Ltd. All chemicals were used
without further purification and modification.
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