Great attention has been paid to silicone-based fouling-release coatings (FRCs) in the realm of maritime antifouling due to their highly efficient and eco-friendly properties, but many challenges remain for developing a silicone-based FRC that improves its adhesion performance without reducing the antifouling property. Herein, a non-toxic silicone-based FRC has been developed by integrating acrylic resin (AR) with a silicon resin (PDMS) to spontaneously form a self-stratified AR/PDMS coating. The AR/PDMS antifouling coating still has the same fouling-release performance but improved adhesion strength (from 0.4 to 2.0 MPa) in comparison with pristine PDMS. Moreover, the antifouling coating has proven to be extremely stable in different environments (such as pH, heating, and ultraviolet exposure). The study provides a facile and convenient self-stratified strategy to develop antifouling coatings, contributing to environmentally friendly coatings in marine applications.

Samples of 17-4PH high-strength steel were processed by selective laser melting (SLM) and solution-processed. The effects of the solution temperature on the microstructure and mechanical properties of the samples were studied. The 17-4PH high-strength steel is primarily composed of martensite, with a small number of austenite phases, and contains many dislocations. After the solution treatment, the grain size gradually increased, yielding typical martensite. The samples were subjected to an aging treatment after the solution treatment. Precipitates formed in the samples, conducive to improving their strength and hardness. The Vickers hardening and wear properties of the 17-4PH high-strength steel samples first increased and then decreased with increasing solution temperature. After the solution treatment at 1040 °C for 2 h and aging at 480 °C for 4 h, the Vickers hardening of the 17-4PH high-strength steel increased to 392 HV0.5, and the friction coefficient was approximately 0.6. These values were, respectively, 7% and 5% higher than those for the untreated samples.

The microstructural evolution, nanosized precipitation behaviors and mechanical properties of a Ti-bearing micro-alloyed steel at different coiling temperatures were studied using optical microstructure (OM), scanning electron micrograph (SEM), transmission electron microscopy (TEM), Vickers hardness and tensile tests. When the coiling temperature was 500 °C, the specimen showed mainly bainitic structure, whereas polygonal ferrite was visible as the coiling temperature increased to 650 °C and 700 °C. The Vickers hardness of tested steel reached the maximum, which can be attributed to the largest number of nanosized precipitates in ferrite at the coiling temperature of 650 °C. A coiling temperature of 650 °C was optimal for the formation of TiC because of the high diffusion rate of alloying elements and kinetics of precipitation. In the laboratory rolling experiment, when the coiling temperature was 630 °C, the steel with yield strength of 682 ± 2.1 MPa and tensile strength of 742 ± 4.9 MPa was produced. The fine-grain strengthening and precipitation strengthening were 262 MPa and 268 MPa, respectively.

This paper investigated the effect of silicon phase morphology and size on microstructure, mechanical properties, and corrosion resistance of the AlSi10Mg alloys fabricated by selective laser melting (SLM). Using different heat treatment conditions for SLM-fabricated alloys, the microstructure characteristics and mechanical properties are analyzed. The corrosion behavior analysis is also performed using potentiodynamic polarization, electrochemical and immersion tests. Results show that the AlSi10Mg alloy directly fabricated by SLM has a continuous eutectic silicon network, which has a small driving force for corrosion and facilitates the deposition of corrosion products and generates a dense protective film. On the contrary, the formation of large isolated and uniformly distributed silicon particles produces a greater corrosion driving force after heat treatment, which makes most of the corrosion products transfer to the solution. The corrosion resistance of AlSi10Mg alloy directly fabricated by SLM is better than that of the alloys with heat treatment. Moreover, the heat treatment reduces the hardness of AlSi10Mg alloys due to the decrease in the solid solution strengthening effect.

TiC/316L stainless steel composites were prepared by selective laser melting. The adhesion work, interface energy and electronic structure of the TiC/γ-Fe interfaces in TiC/316L stainless steel composites were studied to investigate the heterogeneous nucleation potential of γ-Fe grains on TiC particles by using the first principle. The degree mismatch between TiC (001) and γ-Fe (001) interface was lowest. There are four TiC (001)/γ-Fe (001) interface models with different stacking sequences (on-site and bridge-site) and different atomic arrangement sequences (C centre and Ti centre). The results show that the Fe-on-Ti centre interface had the largest work of adhesion (3.87 J/m²) and lower interfacial energy (0.04 J/m²), it was more stable, and the interfacial energy of the model was lower than that of γ-Fe/Fe melt (0.24 J/m²). Strong Fe-C covalent bonds and Fe-Ti metallic bonds were formed near the interface, which increased the interfacial strength, indicating that TiC had strong heterogeneous nucleation potency for γ-Fe.

The Al₄C₃ phase was precipitated via a reaction of graphene (Gr) with Al during selective laser melting (SLM). The interfacial nature of the Gr (0001)/Al₄C₃ (0001) interface was determined using the first-principle calculation. The simulation results showed that the influence of the stacking site on the interfacial structure was limited and the Al-termination interface presented a more stable structure than the C-termination interface. The Al-termination-CH site interface had the largest work of adhesion (6.28 J/m²) and the smallest interfacial distance (2.02 Å) among the four interfacial structures. Mulliken bond population analysis showed that the bonding of the Al-termination interface was a mixture of covalent and ionic bonds and there was no chemical bonding in the C-termination interface.