Source abstract
Abstract
Vinylidene fluoride (VDF)-based copolymers bearing pendant phosphonic acid function for potential application as anticorrosion coatings were synthesized via free radical copolymerization of VDF with a new phosphorus containing 2-trifluoromethacrylate monomer, (dimethoxyphosphoryl)methyl 2-(trifluoromethyl)acrylate (MAF-DMP). MAF-DMP was prepared from 2-trifluoromethacrylic acid in 60% overall yield. Radical copolymerizations of VDF with MAF-DMP initiated by tert -amyl peroxy-2-ethylhexanoate at varying ([VDF] 0 /[MAF-DMP] 0 ) feed ratios led to several poly(VDF- co -MAF-DMP) copolymers having different molar percentages of VDF (79–96%) and number-average molecular weights ( M n ’s) up to ca. 10 000 g mol –1 in fair yields (47–53%). Determination of the composition and microstructure of all the synthesized copolymers was done by 1 H and 19 F NMR spectroscopies. The monomer reactivity ratios of this new VDF/MAF-DMP pair were also determined ( r VDF = 0.76 ± 0.34 and r MAF-DMP = 0 at 74 °C). The resulting poly(VDF- co -MAF-DMP) copolymers exhibited high melting temperature (162–171 °C, with respect to the VDF content), and the degree of crystallinity reached up to 51%. Finally, the pendant dimethyl phosphonate ester groups of the synthesized poly(VDF- co -MAF-DMP) copolymer were quantitatively hydrolyzed, giving rise to novel phosphonic acid-functionalized PVDF (PVDF-PA). In comparison to hydrophobic poly(VDF- co -MAF-DMP) copolymers (the water contact angle, WCA, was 98°), the hydrophilic character of the PVDF-PA was found to be surprisingly rather pronounced, exhibiting low WCA (15°). Finally, steel plates coated with PVDF-PA displayed satisfactory anticorrosion properties under simulated seawater environment.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Ingénierie et Architectures Macromoléculaires Team, Institut Charles Gerhardt, UMR 5253 CNRS, UM, ENSCM, Place Eugène Bataillon, 34095 Montpellier Cedex 5, France
Chimie Moleculaire et Organisation du Solide Team, Institut Charles Gerhardt, UMR 5253 CNRS, UM, ENSCM, Place Eugène Bataillon, 34095 Montpellier Cedex 05, France
Department of Chemistry and Biochemistry, Faculty of Sciences 1, Lebanese University, Rafic Hariri University, Campus − Hadas, Beirut, Lebanon
Funding
Agence Nationale de la Recherche · Agence Universitaire de la Francophonie · Centre National de la Recherche Scientifique · Conseil National de la Recherche Scientifique Libanais