Xia Lei, Li Yan, Zhao Shen, Xiong Sang, Jiang Zhengyi
School of Material and Metallurgy, University of Science and Technology Liaoning, Anshan 114051, China.
Ansteel Iron & Steel Research Institute, Ansteel Group Corporation, Anshan 114009, China.
Materials (Basel). 2020 Nov 3;13(21):4933. doi: 10.3390/ma13214933.
Static corrosion experiments were carried out to investigate the corrosion of each kind of component in the rolling oil on the rolled copper foil. The surface morphology and chemical composition of corrosion products were detected by a digital camera, scanning electron microscope (SEM), energy dispersive spectrometer (EDS) and X-ray photoelectron spectroscopy (XPS). The results showed that the maximum corrosion rate of rolled copper foil in the base stock and friction modifiers (butyl stearate and dodecanol) was close to zero, while that of rolled copper foil in the N-containing borate, phosphate and the fully formulated rolling oil were 0.17, 1.12 and 0.78 mm/a, respectively. The color of rolled copper foil changing from pink into purple-black when corroded in the N-containing borate. The composition of it was mainly CuO and CuO with some N-containing borate adsorbed on it. However, the color and composition of the corroded copper foil in the phosphate were similar to that of the original copper foil. It was complicated for the corroded copper foil in the fully formulated rolling oil, which showed characteristics both in the N-containing borate and in the phosphate according to different positions. It indicated that there might be little corrosion for the base stock and friction modifiers on the rolled copper foil. It might mainly be extreme pressure additives (N-containing borate and phosphate) that caused the corrosion of rolled copper foil. There might be competition between N-containing borate and phosphate for the corrosion of rolled copper foil in the fully formulated rolling oil, resulting in a lower corrosion rate compared with that in the phosphate.
进行了静态腐蚀实验,以研究轧制油中各类成分对轧制铜箔的腐蚀情况。通过数码相机、扫描电子显微镜(SEM)、能谱仪(EDS)和X射线光电子能谱(XPS)检测了腐蚀产物的表面形貌和化学成分。结果表明,轧制铜箔在基础油和摩擦改进剂(硬脂酸丁酯和十二醇)中的最大腐蚀速率接近零,而在含氮硼酸盐、磷酸盐和全配方轧制油中轧制铜箔的腐蚀速率分别为0.17、1.12和0.78mm/a。轧制铜箔在含氮硼酸盐中腐蚀时颜色从粉红色变为紫黑色,其成分主要为CuO以及吸附有一些含氮硼酸盐的CuO。然而,在磷酸盐中腐蚀的铜箔的颜色和成分与原始铜箔相似。在全配方轧制油中腐蚀的铜箔情况较为复杂,根据不同位置呈现出含氮硼酸盐和磷酸盐中的两种特征。这表明基础油和摩擦改进剂对轧制铜箔可能几乎没有腐蚀。可能主要是极压添加剂(含氮硼酸盐和磷酸盐)导致了轧制铜箔的腐蚀。在全配方轧制油中,含氮硼酸盐和磷酸盐在对轧制铜箔的腐蚀方面可能存在竞争,导致其腐蚀速率低于在磷酸盐中的腐蚀速率。