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LOCALIZED AND GENERAL CORROSION OF COPPER IN AZOLES AND SILICA INHIBITED ZERO BLOWDOWN COOLING WATER IN AN AUTOMOTIVE PLANT

机译:在唑类和二氧化硅中铜的局部和一般腐蚀抑制了汽车厂中的零排污冷却水

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In the spring of 2007, the cooling water chemistry at a large automotive plant in Los Angeles, California, was changed from traditional chemical treatment of potable water to recycled water treated with a new zero blowdown chemistry. To establish the localized copper corrosion baseline during this transition, coupled multielectrode array sensors (CMAS) were installed in the sampling station of the cooling water system and corrosion monitoring was performed on real time basis in the plant. The CMAS corrosion monitoring was implemented as a means to rapidly confirm the effectiveness of the new corrosion control technology in protecting copper exchanger tubes in a potential highly corrosive environment. The need for rapid real time confirmation of effective copper corrosion inhibition with CMAS was based on presence of critical copper exchange surfaces in the customer system that would be exposed to the presence of 30 to 40 mg/L of ammonia in the recycled municipal waste water used as tower makeup. Prior experience using linear polarization resistance (LPR) and weight loss methods to determine corrosion rates indicated they were not effective in reliably detecting changes in corrosion in high dissolved solids water with this treatment method, primarily due to the extraordinarily low corrosion rates with this chemistry for steel, copper and other metals. Further, there was no prior monitoring experience with copper exposed to ammonia in high TDS chemistry to indicate that previous low corrosion rates could be maintained with this new chemistry.
机译:2007年春天,加利福尼亚州洛杉矶大型汽车厂的冷却水化学从传统的化学处理从饮用水中的传统化学处理改变,以新的零排污化学治疗的再生水。为了在该转变期间建立局部铜腐蚀基线,耦合的多电极阵列传感器(CMAS)安装在冷却水系统的采样站中,并且在工厂的实时进行腐蚀监测。 CMA腐蚀监测实施为迅速证实新型腐蚀控制技术在潜在高度腐蚀性环境中保护铜交换管的有效性的手段。需要快速实时确认有效铜腐蚀抑制与CMAS的抑制基于客户体系中的关键铜交换表面的存在,该铜交换表面将暴露在循环的市政废水中的30至40mg / L氨的存在下作为塔形化妆。使用线性偏振电阻(LPR)和体重减轻方法的经验,以确定腐蚀速率表明它们在通过这种处理方法中可靠地检测高溶解固体水中腐蚀的变化而无效,主要是由于与该化学的极其腐蚀速率为原因钢,铜和其他金属。此外,在高TDS化学中暴露于氨的铜的先前监测经验表明可以通过这种新化学维持以前的低腐蚀速率。

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