The effect of ZnO nanoparticles (ZnO NPs), with different concentrations in simulated water, on the activity of sulfate-reducing bacteria (SRB) and their adhesion behaviour on stainless-steel surfaces, with and without visible light treatment, were investigated. The results showed that the concentration of ZnO NPs and light treatment greatly influenced the antibacterial performance of the NPs. In the water solution without light treatment, the low concentration (no more than 1 mg/L) of ZnO NPs in the aqueous solution promoted the growth of SRB, and the amount of biofilm attached to the stainless-steel surface increased. As the concentration increased, ZnO NPs exhibited antibacterial effects. In water under visible light irradiation, ZnO NPs showed antibacterial performance at all the concentrations studied (0.5~50 mg/L), and the antibacterial efficiency increased with the increase in the concentration of NPs. The determination results of the reactive oxygen species showed that light treatment can stimulate ZnO NPs in water to generate ·OH and O₂^·−, which exhibited good antibacterial properties. The adhesion amount of SRB on the stainless-steel surface was inversely proportional to the antibacterial efficiency of ZnO NPs.

The formation of CaCO₃ crystals on the cathode surface and the scale-inhibition performance of scale inhibitor 2-phosphonobutane-1,2,4-tricarboxylic acid (PBTCA) on the cathode surface were studied by methods of solution analysis, gravimetric analysis, SEM, FTIR, and XRD techniques. They were then compared with the results of the formation and suppression of CaCO₃ crystals in aqueous solution. PBTCA had a good solution-scale-inhibition performance and good lattice-distortion effects on CaCO₃ crystals in solution, which could change the CaCO₃ from calcite to vaterite and aragonite crystals. The solution-scale-inhibition efficiency exceeded 97% when the PBTCA concentration reached 8 mg/L. Under cathodic polarization conditions, the surface-scale-inhibition efficiency of the cathode and solution-scale-inhibition efficiency near the cathode surface both exceed 97% at polarization potential of −1V. The addition of PBTCA significantly reduced the amount of CaCO₃ crystals formed on the cathode surface and had good surface and solution-scale-inhibition effect. However, the lattice-distortion effect of PBTCA on CaCO₃ crystals disappeared on the cathode surface, and the resulting CaCO₃ contained only calcite crystals. The high-scale-inhibition effect of PBTCA under cathodic polarization was mainly due to the inhibition of the formation of calcium carbonate crystals by PBTCA, and not because of the lattice distortion of CaCO₃ crystals.

The corrosion behavior of brass in TiO₂ and Al₂O₃ nanofluids using a simulated cooling water (SCW) as the base solution and sodium dodecyl benzene sulfonate (SDBS) as the dispersant was studied by electrochemical measurements and surface analysis in this paper. It was found that SDBS could be adsorbed on the brass surface to form a protective film and have a corrosion inhibition effect on brass in SCW. In the SCW-SDBS-TiO₂ nanofluid, some negatively charged TiO₂ nanoparticles were attached to the brass surface and no obvious SDBS adsorption film was found, and the SDBS in this nanofluid had almost no corrosion inhibition on brass. In the SCW-SDBS-Al₂O₃ nanofluid, the brass surface was covered by a uniformly distributed SDBS film containing some Al₂O₃ nanoparticles which were positively charged, and the corrosion inhibition of brass was significantly improved in this nanofluid. It is concluded that the adsorption of SDBS on the brass surface in nanofluids is related to the charge status of the nanoparticles, which makes brass have different corrosion resistance in various nanofluids.