scholarly journals Effect of Direct Fluorination on the Transport Properties and Swelling of Polymeric Materials: A Review

Membranes ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 713
Author(s):  
Nikolay A. Belov ◽  
Dmitrii S. Pashkevich ◽  
Alexandre Yu Alentiev ◽  
Alain Tressaud

Fluorine-containing polymers occupy a peculiar niche among conventional polymers due to the unique combination of physicochemical properties. Direct surface fluorination of the polymeric materials is one of the approaches for the introduction of fluorine into the chemical structure that allows one to implement advantages of fluorinated polymers in a thin layer. Current review considers the influence of the surface interaction of the polymeric materials and membranes with elemental fluorine on gas, vapor and liquid transport as well as swelling and related phenomena. The increase in direct fluorination duration and concentration of fluorine in the fluorination mixture is shown to result mostly in a reduction of all penetrants permeability to a different extent, whereas selectivity of the selected gas pairs (He-H2, H2-CH4, He-CH4, CO2-CH4, O2-N2, etc.) increases. Separation parameters for the treated polymeric films approach Robeson’s upper bounds or overcome them. The most promising results were obtained for highly permeable polymer, polytrimethylsilylpropyne (PTMSP). The surface fluorination of rubbers in printing equipment leads to an improved chemical resistance of the materials towards organic solvents, moisturizing solutions and reduce diffusion of plasticizers, photosensitizers and other components of the polymeric blends. The direct fluorination technique can be also considered one of the approaches of fabrication of fuel cell membranes from non-fluorinated polymeric precursors that improves their methanol permeability, proton conductivity and oxidative stability.

Polymers ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 2836
Author(s):  
Nikolay A. Belov ◽  
Alexander Y. Alentiev ◽  
Yulia G. Bogdanova ◽  
Artem Y. Vdovichenko ◽  
Dmitrii S. Pashkevich

Direct fluorination of polymers is a widely utilized technique for chemical modification. Such introduction of fluorine into the chemical structure of polymeric materials leads to laminates with highly fluorinated surface layer. The physicochemical properties of this layer are similar to those of perfluorinated polymers that differ by a unique combination of chemical resistance, weak adhesion, low cohesion, and permittivity, often barrier properties, etc. Surface modification by elemental fluorine allows one to avoid laborious synthesis of perfluoropolymers and impart such properties to industrial polymeric materials. The current review is devoted to a detailed consideration of wetting by water, energy characteristics of surfaces, adhesion, mechanical and electrical properties of the polymers, and composites after the direct fluorination.


1994 ◽  
Vol 67 (3) ◽  
pp. 277-282 ◽  
Author(s):  
Robert G. Syvret ◽  
Daniel L. Vassilaros ◽  
David M. Parees ◽  
Guido P. Pez

2009 ◽  
Vol 62 (3) ◽  
pp. 232 ◽  
Author(s):  
Mauro Iannelli ◽  
Fabio Bergamelli ◽  
Giancarlo Galli

11-(4,4-Dimethyl-2,5-dioxoimidazolidin-1-yl)undecyl acrylate was synthesized in a two-step procedure using microwave irradiation. Poly(acrylates) containing fluorinated and hydantoin (5,5-dimethylimidazolidine-2,4-dione) moieties were prepared by free radical polymerization of 2-(perfluorooctyl)ethyl acrylate and the synthesized monomer with the aim of obtaining low surface energy polymeric materials with properties of contact-active biocides. Polymeric films were treated with a bleaching solution in order to convert the hydantoin units to N-halamines, well-known contact-active biocides. The reversibility of the chlorination reaction, necessary to impart a renewable biocide effect, was investigated by Fourier Transform-Attenuated Total Reflection. Preliminary biological tests conducted against Bacillus megaterium demonstrated the effective biocide properties of the prepared materials.


2008 ◽  
Vol 12 (2) ◽  
pp. 339-344 ◽  
Author(s):  
Richard D. Chambers ◽  
Graham Sandford ◽  
Jelena Trmcic ◽  
Takashi Okazoe

ChemInform ◽  
2010 ◽  
Vol 27 (15) ◽  
pp. no-no
Author(s):  
R. D. CHAMBERS ◽  
M. P. GREENHALL ◽  
J. HUTCHINSON

ChemInform ◽  
2010 ◽  
Vol 41 (2) ◽  
Author(s):  
Richard D. Chambers ◽  
Takashi Nakano ◽  
Takashi Okazoe ◽  
Graham Sandford

2017 ◽  
Vol 899 ◽  
pp. 36-41 ◽  
Author(s):  
Josiane R. Silvano ◽  
J.M.M. Mello ◽  
Lucinao Luiz Silva ◽  
Humberto Gracher Riella ◽  
Márcio Antônio Fiori

A major challenge in the manufacture of films for polymeric packaging is the definition and setting of the friction coefficient (FCO) for the film surfaces. The FCO values are established with the incorporation of additives during the processing of the polymeric films. But, the homogenization of these additives in the polymeric matrix is very difficult. The additives have different polarity that the matrix polymeric and not are mixable. So, these additives migrate for the surface of the polymeric films easily. Several molecules are used as sliding additives, but among the most efficient are the amides molecules, highlighting the erucamide. This molecule promotes the decrease of the FOC but due its quick migration for the polymeric film surface provides numerous problems for the manufacture of the polymeric packaging and during its application as the product. In this work a nanocomposite (MMT-ERU) was obtained by an intercalation process to improve the compatibility between the polymeric materials and the erucamide molecules. The results shown in this work refers to the studies about the intercalation processes of the erucamide molecules into nanoclays (montmorillonite) to obtain the nanocomposite MMT-ERU. The effect of the temperature and the percentage of the nanoclay in the intercalation processes were studied. The results of x-ray diffraction and differential scanning calorimetry shown that erucamide molecules were intercalated in the nanoclay structures and that intercalation efficiency depends positively of the temperature and percentage amount of the nanoclay in the reaction medium.


2009 ◽  
Vol 189 (2) ◽  
pp. 958-965 ◽  
Author(s):  
Jie-Cheng Tsai ◽  
Hui-Pin Cheng ◽  
Jen-Feng Kuo ◽  
Yao-Hui Huang ◽  
Chuh-Yung Chen

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