Thermoresponsive Amphiphilic Block Copolymer-Stablilized Gold Nanoparticles: Synthesis and High Catalytic Properties.

A series of novel well-defined 8-hydroxyquinoline (HQ)-containing thermoresponsive amphiphilic diblock copolymers {poly(styrene- co-5-(2-methacryloylethyloxy-methyl)-8-quinolinol)- b-poly( N-isopropylacrylamide) P(St- co-MQ)- b-PNIPAm (P1,2), P(NIPAm- co-MQ)- b-PSt (P3,4)} and triblock copolymer poly( N-isopropylacrylamide)- b-poly(methyl-methacrylate- co-5-(2-methacryloylethyloxymethyl)-8-quinolinol)- b-polystyrene PNIPAm- b-P(MMA- co-MQ)- b-PSt (P5) were prepared by reversible addition-fragmentation chain-transfer (RAFT) polymerization, and their self-assembly behaviors were studied. Block copolymer P1-P5-stabilized gold nanoparticles (Au@P1-Au@P5) with a small size and a narrow distribution were obtained through the in situ reduction of gold precursors in an aqueous solution of polymer micelles with HQ as the coordination groups. The resulting Au@P nanohybrids possessed excellent catalytic activity for the reduction of nitrophenols using NaBH4. The size, morphology, and surface chemistry of Au NPs could be controlled by adjusting the structure of block polymers with HQ in different block positions, which plays an important role in the catalytic properties. It was found that longer chain lengths of hydrophilic or hydrophobic segments of block copolymers were beneficial to elevating the catalytic activity of Au NPs for the reduction of nitrophenols, and the spherical nanoparticles (Au@P5) stabilized with triblock copolymers exhibit higher catalytic performance. Surprisingly, the gold nanowires (Au@P4) produced with P4 have the highest catalytic activity due to a large abundance of grain boundaries. Excellent thermoresponsive behavior for catalytic reaction makes the as-prepared Au@P hybrids an environmentally responsive nanocatalytic material.

Study on the Water Absorption Characteristics of Anthracite Particles after Immersion in Water.

Reducing pollution caused by coal dust has always been a hot issue in the coal mining industry, and the water absorption of coal particles plays an important role in dust reduction. To study the relationship between different immersion time and the water absorption of coal particles, the substance content of coal particles after immersion was analyzed and water absorption characterization of coal particles was carried out by X-ray diffraction (XRD), water absorption calculations, and water absorption measurements. The results indicate that immersion can alter the material content of coal particles, leading to a decrease in the content of soluble mineral kaolinite, thereby affecting the wettability of coal particles. Notably, the longer the immersion time, the higher the water absorption rate of the particles, indicating a more significant water absorption effect. Furthermore, there is a negative correlation between particle sizes and water absorption of coal particles. The research results provide a theoretical reference for reducing coal dust pollution and improving the efficiency of dust suppression through spray.

Mussel-Inspired Catechol-Formaldehyde Resin-Coated Fe3O4 Core-Shell Magnetic Nanospheres: An Effective Catalyst Support for Highly Active Palladium Nanoparticles.

Magnetic Fe3O4@catechol-formaldehyde resin (CFR) core-shell nanospheres were fabricated via a controllable hydrothermal method. The shell thickness of Fe3O4@CFR nanospheres can be effectively regulated in the range of 10-170 nm via adjusting reaction parameters. In particular, catechol groups on the surface of nanospheres also play a significant role in mussel-inspired chemistry to further combine with graphene oxide (GO) to wrap the Fe3O4@CFR spheres. The obtained Fe3O4@CFR and Fe3O4@CFR@GO nanospheres can be used as the effective catalyst supports of small Pd nanoparticles (PdNPs, <10 nm) formed via an in situ synthesis route. The as-fabricated nanohybrid catalysts of Fe3O4@CFR@PdNPs and Fe3O4@CFR@GO@PdNPs with excellent dispersibility and stability are reusable after magnetic separation from catalytic systems. In particular, a super active performance was demonstrated for the catalytic reduction of methylene blue dye with highest turnover frequency (5260 min-1) yet reported in the literature using a very low dosage of the Fe3O4@CFR@GO@PdNP catalyst. In addition, the Fe3O4@CFR@GO@PdNP catalyst also exhibits a highly catalytic efficiency for the Suzuki coupling reaction using pure water as a green solvent at room temperature.

Mussel-inspired construction of thermo-responsive double-hydrophilic diblock copolymers-decorated reduced graphene oxide as effective catalyst supports for highly dispersed superfine Pd nanoparticles.

Well-dispersed ultrafine palladium nanoparticles supported by reduced graphene oxide functionalized with catechol-terminated thermo-responsive block copolymer (PdNPs@BPrGO) were successfully constructed for highly efficient heterogeneous catalytic reduction. We first synthesized a novel temperature-responsive episulfide-containing double-hydrophilic diblock copolymer, poly(poly(ethylene glycol) methyl ether methacrylate-co-2,3-epithiopropyl methacrylate)-block-poly(N-isopropylacrylamide) (P(PEGMA-co-ETMA)-b-PNIPAM), through a reversible addition-fragmentation chain transfer (RAFT) polymerization utilizing a chain-transfer agent with a catechol unit as the end group. The obtained block copolymers can be facilely anchored to the surface of GO via mussel-inspired chemistry. The PdNPs were loaded on GO decorated with block copolymer brushes (BPrGO) as a support via the in situ reduction of palladium precursors with the episulfide ligands of the block copolymer as a stabilizer. The resulting PdNPs@BPrGO nanohybrid catalyst had good water dispersibility and stability. Furthermore, a low dosage of PdNPs@BPrGO catalyst exhibited excellent catalytic performance in the reduction of methylene blue and nitrophenols. The performance was attributed to the ability of PdNPs@BPrGO to facilitate the diffusion of reactants compared to PdNPs@GO without polymer modification. PdNPs@BPrGO also possessed an interesting temperature-responsive catalytic property due to the reversible "coil-to-globule" phase transition behaviour of PNIPAM blocks onto the surface of catalyst. The PdNPs@BPrGO catalyst was successfully recovered and reused five times without any detectible loss in catalytic activity, demonstrating its great potential in a wide range of industrial catalytic applications.