Impact-sliding caused by random vibrations between tubes and supports can affect the operation of heat exchangers. In addition, a corrosive environment can cause damage, accelerating the synergism of corrosion and wear. Therefore, the focus of this work was the impact-sliding fretting tribocorrosion behavior of 316L heat exchanger tubes at different halide concentrations. A device system incorporating the in situ electrochemical measurements of impact-sliding fretting corrosion wear was constructed, and experiments on 316L heat exchanger tubes in sodium chloride (NaCl) solution with different concentrations (0.0, 0.1, 0.5, 1.0, 3.5, and 5.0 wt%) were carried out. The synergism between wear and corrosion was also calculated and analyzed. The wear and damage mechanisms were elucidated by correlating the corrosion-wear synergism, morphologies, and material loss rates. The results indicated that the stable wear stage occurred at approximately 9–12 h, after which the corrosion current increased with the expansion of the wear area. As the halide concentration increased, the scale of damage on the wear scars gradually decreased, changing from being dominated by cracks, delaminations, and grooves to being dominated by scratches, microgrooves, and holes. There was an obvious positive synergism between wear and corrosion. The material loss was dominated by pure mechanical wear and wear enhanced by corrosion, but corrosion enhanced by wear contributed more than tangential sliding fretting corrosion. The total mass loss increased gradually in the range of 0.0–0.5 wt% and decreased in the range of 0.5–5.0 wt%. Large-scale damage enhanced by corrosivity and small-scale damage reduced by lubricity dominated the material loss at low and high concentrations, respectively.
Bacterial infection is currently considered to be one of the major reasons that leads to the failure of guided bone regeneration (GBR) therapy. Under the normal condition, the pH is neutral, while the microenvironment will become acid at the sites of infection. Here, we present an asymmetric microfluidic/chitosan device that can achieve pH-responsive drug release to treat bacterial infection and promote osteoblast proliferation at the same time. On-demand release of minocycline relies on a pH-sensitive hydrogel actuator, which swells significantly when exposed to the acid pH of an infected region. The PDMAEMA hydrogel had pronounced pH-sensitive properties, and a large volume transition occurred at pH 5 and 6. Over 12 h, the device enabled minocycline solution flowrates of 0.51–1.63 µg/h and 0.44–1.13 µg/h at pH 5 and 6, respectively. The asymmetric microfluidic/chitosan device exhibited excellent capabilities for inhibiting Staphylococcus aureus and Streptococcus mutans growth within 24 h. It had no negative effect on proliferation and morphology of L929 fibroblasts and MC3T3-E1 osteoblasts, which indicates good cytocompatibility. Therefore, such a pH-responsive drug release asymmetric microfluidic/chitosan device could be a promising therapeutic approach in the treatment of infective bone defects.