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In-situ 2D maps of pH shifts across brass-lead galvanic joints using microelectrodes

机译:使用微电极在黄铜-铅电接头之间的pH值变化的原位二维图

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摘要

Galvanic corrosion in drinking water distribution systems, such as conditions following partial lead (Pb) service line replacement, has received recent attention. In order to better understand conditions at galvanic connections that lead to enhanced metal release and provide remedial strategies, the water-metal and anodic-cathodic interfaces at these locations must be better understood. In this paper, a pH microelectrode system was used to create in-situ 2D spatial images of the pH of water across two brass coupons connected by a leaded solder joint at 100 μm above the metal’s surface under flowing and stagnation conditions. Water stagnation resulted in significant pH changes across the surfaces compared to flow condition. Under stagnation, the pH above the anode (leaded solder) was 1.5 pH units below the bulk water and as much as 2.5 units below the cathode (brass). These conditions can enhance lead release at the anode, which reflects different anodic-cathodic relationships of coupled metals primarily controlled by water flow. Most importantly, this work has demonstrated the ability to make real pH measurement at the surface of corroding metals using a novel microelectrode approach.
机译:饮用水分配系统中的电偶腐蚀,例如更换部分铅(Pb)服务管线后的状况,最近受到关注。为了更好地了解导致金属释放增加并提供补救策略的电连接条件,必须更好地了解这些位置的水-金属和阳极-阴极界面。在本文中,使用pH微电极系统在流动和停滞条件下,通过金属表面上方100μm处的铅焊接头连接的两个黄铜试样之间,创建了水pH值的原位二维空间图像。与流动条件相比,水的停滞导致整个表面的pH值发生明显变化。在停滞状态下,阳极(含铅焊料)上方的pH值比大量水低1.5个pH单位,而阴极(黄铜)下方的pH则最多2.5个单位。这些条件可以增强阳极处的铅释放,这反映了主要受水流控制的耦合金属的不同阳极-阴极关系。最重要的是,这项工作证明了使用新颖的微电极方法在腐蚀金属表面进行真实pH测量的能力。

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