Anticorrosion Performance of PVDF Membranes Modified by Blending PTFE Nanoemulsion and Prepared through Usual Non-Solvent-Induced Phase Inversion Method

In this study, PVDF/PTFE composite membranes were prepared by adding a PTFE nanoemulsion to a PVDF solution and casting it through the conventional non-solvent-induced phase separation method. The objective was to explore the effectiveness of using a simple and economical method to modify PVDF membranes with PTFE to enhance their anticorrosion performance, especially under highly acidic or alkaline conditions. PTFE nanoparticles (of around 200 nm in size) in nanoemulsion form were blended with PVDF at a mass ratio of PTFE:PVDF in the range of 0–0.3:1. The obtained membranes were examined to determine the effect of the added PTFE nanoparticles on the structure of the modified PVDF membranes as well as on their mechanical strength and surface characteristics. The membranes were then immersed in various concentrations of acidic or alkaline solutions for varied durations ranging from a few days up to as long as 180 days (6 months). The impacts of by the corrosive solutions on the tensile strength, surface roughness, and water flux of the membranes with different exposure times were quantified. The results showed that although a certain extent of change may occur with extended immersion times, greatly enhanced anticorrosion performance was obtained with the prepared PVDF/PTFE membranes compared with the unmodified PVDF membrane. For example, after being immersed in 5 mol-H+··L−1 H2SO4, HCl, and HNO3 solutions for 6 months, the tensile strength at breaking point remained at up to 69.70, 74.07, and 71.38%, respectively, of the initial strength for the PVDF/PTFE (M30) membrane. This was in contrast to values of only 55.77, 70.43, and 61.78% for the unmodified PVDF membrane (M0). Although the water flux and surface roughness showed a change trends to the tensile strength, the PVDF/PTFE (M30) membrane had much higher stability than the PVDF (M0) membrane. In a continuous filtration experiment containing H2SO4 at 0.01 mol-H+·L−1 for 336 h (14 days), the PVDF/PTFE membrane showed a maximum flux change of less than 30%. This was in comparison with a change of up to 50% for the PVDF membrane. However, the PVDF/PTFE membranes did not seem to have a greatly enhanced anticorrosion performance in the alkaline solution environment tested.

Influence of Electrolyte Temperature on Morphology and Properties of Composite Anodic Film on Titanium Alloy Ti-10V-2Fe-3Al

In this study, we introduced a novel environmentally-friendly electrolyte consisting of polytetrafluoroethylene (PTFE) nanoparticles and malic acid solution to fabricate composite anodic film on Ti-10V-2Fe-3Al alloy at different electrolyte temperatures. The morphology revealed that the PTFE nanoparticles were successfully incorporated into composite anodic films and embedded preferentially in the pores and cracks. Their performances (wear, corrosion and hydrophobicity) were evaluated via electrochemical tests, ball on disc tests, and a contact angle (CA) meter. Compared to the substrate of titanium alloy Ti-10V-2Fe-3Al, the composite anodic films exhibited the low wear rates, high corrosion resistance and good hydrophobicity. However, the microstructure and morphology of the films were affected by the electrolyte temperature. As a result, their performances were changed greatly as a function of the temperature and the film fabricated at 20 °C exhibited better performances (CA = 131.95, icorr = 6.75 × 10−8 A·cm−2, friction coefficient = 0.14) than those at other electrolyte temperatures. In addition, the corresponding lubrication mechanism of the composite anodic films was discussed.

Highly durable fuel cell catalysts using crosslinkable block copolymer-based carbon supports with ultralow Pt loadings

The catalyst in which carbon shells encapsulate PtFe nanoparticles shows superior activity and durability for proton exchange membrane fuel cells.

Biomimetic catechol-based adhesive polymers for dispersion of polytetrafluoroethylene (PTFE) nanoparticles in an aqueous medium

Biomimetic synthetic functional materials are valuable for a large number of practical applications with improved or tunable performance.

Modulating Catalytic Activity and Durability of PtFe Alloy Catalysts for Oxygen Reduction Reaction Through Controlled Carbon Shell Formation

Demand on synthetic approaches to high performance electrocatalyst with enhanced durability is increasing for fuel cell applications. In this work, we present a facile synthesis of carbon shell-coated PtFe nanoparticles by using acetylacetonates in metal precursors as carbon sources without an additional polymer coating process for the carbon shell formation. The carbon shell structure is systematically controlled by changing the annealing conditions such as the temperature and gas atmosphere. PtFe catalysts annealed at 700 °C under H2-mixed N2 gas show much higher oxygen reduction reaction (ORR) activity and superior durability compared to a Pt catalyst due to the ultrathin and porous carbon shells. In addition, when increasing the annealing temperature, the carbon shells encapsulating the PtFe nanoparticles improves the durability of the catalysts due to the enhanced crystallinity of the carbon shells. Therefore, it is demonstrated that the developed hybrid catalyst structure with the carbon shells not only allows the access of reactant molecules to the active sites for oxygen reduction reaction but also prevents the agglomeration of metal nanoparticles on carbon supports, even under harsh operating conditions. The proposed synthetic approach and catalyst structure are expected to provide more insights into the development of highly active and durable catalysts for practical fuel cell applications.