Developing new coating modification technology of aluminum nitride (AlN) powder for higher hydrolysis resistance is the key to prepare high-performance AlN ceramic substrate with water-based wet process in the future. In the this paper, The poly(vinyl pyrrolidone)-b-poly(Styrene/Itaconic anhydride) (PVP-b-P(St/ITA))block copolymer with PVP as the independent chain segment was designed and synthesized through reversible addition fragmentation chain transfer (RAFT) polymerization, which was used for the study on coating modification, hydrolysis resistance, and dispersion performance of AIN powder. The study results show that, when using PVP macromolecular chain transfer agent (PVP-CTA) for the RAFT chain extension and polymerization in St/ITA binary system, the molecular weight increases linearly and the molecular weight distribution tends to decrease with the monomer conversion rate, which is in line with the activity-controlled characteristics of RAFT polymerization. The copolymer PVP-b-P(St/ITA) was used to for surface modification treatment of submicron AlN powder to generate esterification reaction, which was absorbed and bound to the powder surface. Hydrolysis resistance and dispersion experiments were conducted for modified powder, and the crystal phase and micro structure of modified powder were analyzed and observed through XRD, SEM, and TEM. It was found that copolymer modification had no effect on the powder crystal phase. A 8–21 nm passivation layer was coated on the surface, which can exist stably for 10 h in 60 °C water. Zeta potential and laser particle analyzer tests showed that modified powder featured excellent water-based slurry dispersion performance, and certain self-dispersing characteristics. The highest Zeta potential appeared in pH 6~7, and the particle granularity was distributed uniformly with the median particle diameter of 875 nm. The powder hydrolysis resistance and dispersion performance are significantly improved. 相似文献
Polymer brushes have a large potential for controlling properties such as surface lubrication or wetting through facile functionalization. Polymer chemistry, chain density, and length impact on the wetting properties of brushes. This study explores the use of diblock copolymer brushes with different block length and spatial arrangement of the blocks to tune surface wettability. Block copolymer brushes of the polyelectrolyte [2‐(methacryloyloxy)ethyl] trimethylammonium chloride (PMETAC) with a contact angle of 17° and a hydrophobic block of 1H, 1H, 2H, 2H‐perfluorodecyl Acrylate (PPFDA) with a contact angle of 130° are synthesized by RAFT polymerization. By changing the sequence of polymerization either block is synthesized as top or bottom block. By varying the concentration of initiator the length of the blocks is varied. Contact angle values with intermediate values between 17° and 130° are measured. In addition, by changing solvent pH and in presence of a different salt the contact angle of the copolymer brushes can be fine tuned. Brushes are characterized by atomic force microscopy, Raman confocal microscopy, and X‐ray photoelectron spectroscopy.
Amphiphilic hyperbranched poly(amino ester)s with hydrophilic multi‐ethoxylated triacrylate backbone and hydrophobic long alkyl side chain were firstly synthesized via one pot Michael addition polymerization. The poly‐(amino ester) could dissolve in cold water and self‐assemble into loose micelle. Under 50–1000 ms bubble, the dynamic surface tension (DST) of the poly(amino ester) aqueous solution (0.5 wt%) still maintained in the range of 32–28 mN/m. The aqueous solutions of poly(amino ester)s with different molecular weights showed the lower critical solution temperature (LCST) in the range of 8–50°C, which could also be tuned by its pH. Capped with hydrophobic groups on the terminal units and partially neutralized with acid, the poly(amino ester)s still kept their stable dynamic surfactant behaviors, indicating promising application. 相似文献
Cationic star polymers as drug/gene carriers have attracted increasing attention. Herein, environmental sensitivities and star-shaped architecture were combined into a well-defined gene carrier system, and further amphiphilic modification was conducted. The thermo- and pH-sensitive behaviors of poly[N,N-(dimethyl amino)ethyl methacrylate] (PDMAEMA) star polymers before and after amphiphilic modification in aqueous solutions were investigated. The observed lower critical solution temperature (LCST) increased with increasing arm length due to the increase of hydrophilicity. A significant decrease of the LCSTs with increasing pH and ionic-strength of the solution was found. The incorporation of MMA and BA lipophilic moieties decreased the LCST of the cationic star polymer due to enhanced hydrophobic interaction. As a potential gene carrier, the performance of star polymers on binding DNA was primarily evaluated via particle size, zeta potential, and gel retardation measurements. All the complexes formed stable small particles with diameter of 100～150 nm at N/P ratio higher than 3.0. The electrostatic screening effect and facilitation for the interaction of complexes with cell membrane induced by the incorporation of lipophilic units were expected to enhance the gene transfection efficiency. 相似文献
