RESUMO
This study reports the synthesis of a novel superplasticizer, poly(poly(ethylene glycol)methacrylate)-poly(vinylphosphonic acid) (PPEGMA-PVPA), containing phosphate moieties via solution radical polymerization. By adjusting the feed ratios of monomers, PPEGMA-PVPA copolymers with different phosphate group densities were obtained, and their chemical structure was characterized via FT-IR, 1H NMR spectroscopy and ICP-OES. The results demonstrated that about 70% of the VPA monomer was polymerized. The thermostability of PPEGMA-PVPA was also determined through DSC and TGA. The adsorption-dispersion performance onto cement pastes was investigated using mini-slump test, TOC and zeta potential analysis. It was demonstrated that the adsorption capacity of PPEGMA-PVPA onto cement paste was about 1.4 times stronger than that of the reference polycarboxylate superplasticizer and exhibited excellent adsorption-dispersion performance.
RESUMO
The compelling integration of superhydrophobic coatings with light-to-heat conversion capabilities has garnered substantial interest due to their dual functionality encompassing passive anti-icing and deicing attributes. However, the insufficient mechanical stability and the environmental and human health concerns stemming from the extensive use of organic solvents limit their practical application. In this study, an all-waterborne superhydrophobic photothermal coating (PCPAS) was prepared through the synergy of composite micro-nanoparticles derived from carbon nanotubes (CNT), polydopamine (PDA), and Ag particles with fluorine-containing polyacrylic emulsion (PFA). The PDA provided active sites for Ag+ reduction reaction and enhanced the interfacial interaction between CNT and Ag particles. The interfacial enhancement enabled the coating to maintain stable superhydrophobicity after 260 times sandpaper abrasion and 240 times tape peeling. Simultaneously, the composite micro-nanoparticle's light-to-heat conversion ability gave the coating excellent anti-icing/deicing capabilities. Under the condition of -20 °C, the freezing time of 30 µL of water droplets was extended to 392 s, and 2 × 2 × 2 cm ice cubes placed on the surface of the coating could completely melt after only 1142 s under simulated sunlight irradiation with a 1 kW/m2 intensity. In addition, the coating also had suitable self-cleaning properties and substrate applicability. The comprehensive attributes of this all-waterborne photothermal superhydrophobic coating render it a promising contender for anti-icing and deicing applications in challenging outdoor environments.
RESUMO
Modulating controlled radical polymerization is an interesting and important issue. Herein, modulating RAFT polymerization employing photosensitive azobenzenes is achieved. In the presence of azobenzenes and with visible light off, RAFT polymerization runs smoothly and follows a pseudo-first-order kinetics. In contrast, with light on, RAFT polymerization is greatly decelerated or quenched depending on the type and concentration of azobenzenes. Switchable RAFT polymerization of different (meth)acrylate monomers alternatively with light off and on is demonstrated. A mechanism of photoregulating RAFT polymerization involving radical quenching by azobenzenes is proposed.
RESUMO
Polymeric multicompartment nanoparticles (MCNs) of µ-ABC miktoarm star polymers composed of poly(N,N-dimethylacrylamide) (PDMA), poly(butyl methacrylate) (PBMA), and polystyrene (PS) were synthesized by Cu(I)-catalyzed click reaction and seeded RAFT dispersion polymerization. The synthesized MCNs have a solvophobic PBMA core with separate segregated PS microdomains and a solvophilic PDMA corona. The size and/or morphology of MCNs are correlative to the length of PDMA, PBMA, and PS segments. Ascribed to the characteristic structure, MCNs of µ-DBS can decrease interfacial tension in n-hexane/water, which is much superior to linear diblock copolymer nanoassemblies.
