Surface chemical characterization of deactivated low-level mercury catalysts for acetylene hydrochlorination

Mercury-containing catalysts are widely used for acetylene hydrochlorination in China. Surface chemical characteristics of the fresh low-level mercury catalysts and spent low-level mercury catalysts were compared using multiple characterization methods. Pore blockage and active site coverage caused by chlorine-containing organics are responsible for catalyst deactivation. The reactions of chloroethylene and acetylene with chlorine free radical can generate chlorine-containing organic species. SiO_2 and functional groups on activated carbon contribute to the generation of carbon deposition. No significant reduction in the total content of mercury was observed after catalyst deactivation, while there was mercury loss locally. The irreversible loss of HgCl_2 caused by volatilization, reduction and poisoning of elements S and P also can lead to catalyst deactivation. Si, Al, Ca and Fe oxides are scattered on the activated carbon. Active components are still uniformly absorbed on activated carbon after catalyst deactivation.

Deposition behavior of residual aluminum in drinking water distribution system：Effect of aluminum speciation

Finished drinking water usually contains some residual aluminum.The deposition of residual aluminum in distribution systems and potential release back to the drinking water could significantly influence the water quality at consumer taps.A preliminary analysis of aluminum content in cast iron pipe corrosion scales and loose deposits demonstrated that aluminum deposition on distribution pipe surfaces could be excessive for water treated by aluminum coagulants including polyaluminum chloride（PACl）.In this work,the deposition features of different aluminum species in PACl were investigated by simulated coil-pipe test,batch reactor test and quartz crystal microbalance with dissipation monitoring.The deposition amount of non-polymeric aluminum species was the least,and its deposition layer was soft and hydrated,which indicated the possible formation of amorphous Al（OH）3.Al（13） had the highest deposition tendency,and the deposition layer was rigid and much less hydrated,which indicated that the deposited aluminum might possess regular structure and self-aggregation of Al（13）could be the main deposition mechanism.While for Al（30）,its deposition was relatively slower and deposited aluminum amount was relatively less compared with Al（13）.However,the total deposited mass of Al（30） was much higher than that of Al（13）,which was attributed to the deposition of particulate aluminum matters with much higher hydration state.Compared with stationary condition,stirring could significantly enhance the deposition process,while the effect of pH on deposition was relatively weak in the near neutral range of 6.7 to 8.7.

Hot corrosion behaviors of 921A alloy and HVAF-sprayed Fe-based amorphous coating covered with KCl-ZnCl_(2) salts

Hot corrosion behaviors of the 921A alloy and Fe-based amorphous coating induced by KCl-10% ZnCl_(2) and KCl-55% ZnCl_(2) salts at 450℃ in air for 40 h were investigated.Results show that the 921A alloy suffers more serious corrosion damage than the coating and KCl-55% ZnCl_(2) salts are more corrosive than KCl-10% ZnCl_(2) salts.In the two salts,an Fe_(2)O_(3) layer is formed on the 921A alloy surface,while an outer Fe-rich oxide layer and an inner Cr-rich oxide layer are formed on the surface of the coating.Moreover,a certain amount of metal chloride can be found at the oxide/alloy(coating)interface,which can be explained by "active oxidation".However,the corrosion resistance of the Fe-based amorphous coating did not achieve the desired results,probably because the intersplats in the coating serve as corrosion diffusing channels,which facilitate the corrosion damage rate.Nevertheless,the coating is still in amorphous state after hot corrosion exposure.