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AbstractThe wet desulfurization yields slurry with a moderate temperature and stable supply and thus holds promise for waste heat utilization. However, the corrosive nature and solid particle content of desulfurization slurry from the wet desulfurization process pose potential erosion challenges in waste heat utilization heat exchangers, which is an aspect scarcely explored in the existing literature. The present study aimed to investigate the erosion characteristics in desulfurization slurry heat exchangers using numerical simulation approaches, which can offer crucial insights for practical application in low-grade energy recovery. The result identified slurry mass flow rate and composition as essential factors of erosion distribution. Higher mass flow rates enhance heat transfer efficiency. Still, paradoxically, lower flow rates lead to more pronounced erosion, with a slurry mass flow rate of 35 kg/s resulting in nearly double the erosion compared to the benchmark condition of 56 kg/s. This phenomenon is ascribed to lower fluid velocities in the heat tubes, where the influence of changed velocity diminishes, but slurry exhibits more stable flow at higher mass flow rates. Furthermore, it is also observed that both elevated solids content and particle size lead to an increase in erosion rates. The difference in erosion caused by solid particles with particle sizes in the range of 200–350 µm is marginal. The heat exchanger structure and arrangement also impact fluid flow and erosion. While the difference in fluid flow between vertically and horizontally arranged heat exchangers is negligible, the erosion was significantly reduced to 1/10 in the vertical arrangement. The no-tube-in-window heat exchangers, designed to minimize vibration, exhibit reduced heat transfer capacity alongside diminished and more uniform erosion. The augmentation of tube passes reduces overall erosion but focalizes severe erosion at the slurry inlet, which presents a potential design solution. [ABSTRACT FROM AUTHOR]

A Ag 3 PO 4 /GO/UiO-66-NH 2 (AGU) composite photocatalyst was prepared by an ultrasonic-assisted in situ precipitation method. The optical property, structure, composition, and morphology of photocatalysts were investigated using UV-vis diffuse reflectance spectroscopy, photoluminescence spectroscopy, electrochemical impedance spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, energy-dispersive spectrometry, transmission electron microscopy, Fourier transform infrared spectroscopy, and charge flow tracking by photodeposition of Pt and PbO 2 nanoparticles. In comparison with Ag 3 PO 4 and Ag 3 PO 4 /UiO-66-NH 2 (AU), the AGU composite photocatalyst showed heightened photocatalytic performance for the degradation of levofloxacin hydrochloride (LVF). The AGU photocatalyst (dosage: 0.8 g/L) with 1% mass content of graphene oxide (GO), the mass ratio of Ag 3 PO 4 and UiO-66-NH 2 (U66N) reached 2:1, showed the highest photodegradation rate of 94.97% for 25 mg/L LVF after 60 min of visible light irradiation at pH = 6. The formation of a heterojunction and the addition of GO synergistically promote faster separation of electron-hole pairs, retain more active substances, and enhance the performance of the photocatalyst. Furthermore, the mechanism of the Z-scheme of the AGU composite photocatalytic is proposed.