Compromise Between Bromate Ion Formation and Pesticides Degradation and/or Manganese Removal

Ozonation is a widely used technology within the water industry. Bromate ion formed by oxidation of water containing bromide ion was studied with the Gas Ozone Test and Pilot Scale Ozonation. Bromate ion formation was investigated along with the removal of triazines and/or manganese. Under identical conditions of ozonation, BrO₃ ^? formation is specific for each water and depends on parameters such as Total Organic Carbon, UV absorbance at 254 nm, applied ozone and ozone residual. Pesticides degradation by ozonation alone cannot be achieved without the formation of BrO₃ ^? at a high concentration. Hydrogen peroxide, at a constant ozone dose, reduces the BrO₃ ^? formation. However, even with the use of hydrogen peroxide, the concentration of BrO₃ ^? can remain in excess of the provisional Maximum Contaminant Level (10 μg/L). For certain types of water, pesticide degradation is difficult to achieve if the MCL for BrO₃ ^? has to be met. Manganese oxidation by ozone appears to be achieved without high bromate formation; indeed the presence of manganese hinders BrO₃ ^? formation.     

超音速等离子喷涂制备金属陶瓷涂层的抗冲蚀性能

通过高效能超音速等离子喷涂(SAPS)制备WC-Co及WC-Ni Cr金属陶瓷涂层,对比研究了2种涂层的抗冲蚀性能及在热腐蚀条件下的结构和性能演变。结果表明:2种涂层在喷涂过程中均会发生一定程度的脱碳,表现为W_2C相的形成;同时在WC-Co涂层中有少量的Co_3W_3C和Co_6W_6C相生成,且该涂层在热腐蚀后表层的WC相出现了分解与氧化,形成了W_3C、W_6C_(2.54)等脱碳相与CoWO_4、WO_3等氧化物相。在普通冲蚀条件下,WC-Co涂层的抗冲蚀性能更为优异,但热腐蚀会极大降低WC-Co涂层的抗冲蚀性能;与之相反,WC-NiCr涂层中的NiCr相在热腐蚀环境下生成的Cr_2O_3可以有效阻挡涂层内部与外部之间的物质扩散,从而降低了热腐蚀对涂层结构的破坏,在热腐蚀条件下表现出了优良的抗冲蚀性能。     

Mechanistic Investigation of the Gold-catalyzed Aerobic Oxidation of Alcohols

The mechanism for the gold-catalyzed aerobic oxidation of alcohols was studied using a series of para-substituted benzyl alcohols (Hammett methodology). The competition experiments clearly show that the rate-determining step of the reaction involves the generation of a partial positive charge in the benzylic position (i.e. hydride abstraction). This was further substantiated by the determination of a significant kinetic isotope effect (k_H/k_D = 1.41), when employing an alcohol substrate deuterated in this position.     

Glycerol transformations on polysaccharide derived mesoporous materials

New polysaccharide based solid acids are excellent catalysts for selective chemical transformations of glycerol. Reasonable selectivities to mono-, di- and triacetylated glycerols can be obtained by controlled microwave activation of glycerol–acetic and solid acid mixtures. Etherifications of glycerol using a range of alcohols have also been achieved and with a degree of selectivity to both 1- and 2-positions. The use of the Starbon^® material as a support for palladium further extends the range of heterogeneous catalysed chemistry to the selective oxidations of glycerol to both glycolic and oxalic acids. In all of the reactions, the catalysts can be easily recovered and reused with only a small loss in activity.