对流依赖的氢对碳钢片的渗透

K. Fushimi, Misako Jin, T. Nakanishi, Y. Hasegawa, T. Kawano, M. Kimura
{"title":"对流依赖的氢对碳钢片的渗透","authors":"K. Fushimi, Misako Jin, T. Nakanishi, Y. Hasegawa, T. Kawano, M. Kimura","doi":"10.1149/2.011406EEL","DOIUrl":null,"url":null,"abstract":"Experimental A carbon steel sheet of 0.015 wt% and thickness of 1 mm was used as a specimen. Both sides of each specimen sheet were ground and flattened until 0.05-0.80 mm by mechanical polishing finally using colloidal silica particles of 0.05 μm. The thickness variation of speci- men sheet was controlled within 5%. The back side was electroplated with a nickel layer of 0.5 μm in thickness by cathodic polarization at 0.1 A cm −2 in a Watt's bath (1 mol dm −3 NiSO4 + 0.2 mol dm −3 NiCl2 + 0.6 mol dm −3 H3BO3) at 323 K. Fig.1is a schematic diagram of a Devanathan-Stachurski cell used in this study. The specimen sheet was sandwiched between the two electrochemical cells made from acrylic glass with two O-rings and connected with two potentiostats as working electrodes. The front and back sides of the sample sheet served as hydrogen entry and exit electrodes, respectively. Each cell had a platinum counter electrode and an Ag/AgCl/saturated KCl reference electrode with a Luggin- Haber capillary. The electrolyte in both cells was pH 8.4 boric-borate buffer solution deaerated by bubbling pure Ar gas. The electrolyte in the hydrogen entry side cell was flowed by using a bimorph pump at a constant or sinusoidally pertubated volume flow rate in the range of 0.145-1.50 cm 3 s −1 , while the electrolyte in the cell for the hydrogen exit side was stagnant. During the potentiostatic polarization of entry and exit electrodes, currents flowing through both electrodes were recorded with the electrolyte flow rate using a PC controlled by a LabVIEW (National Instruments) program.","PeriodicalId":11470,"journal":{"name":"ECS Electrochemistry Letters","volume":"3 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1149/2.011406EEL","citationCount":"5","resultStr":"{\"title\":\"Convection-Dependent Hydrogen Permeation into a Carbon Steel Sheet\",\"authors\":\"K. Fushimi, Misako Jin, T. Nakanishi, Y. Hasegawa, T. Kawano, M. Kimura\",\"doi\":\"10.1149/2.011406EEL\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Experimental A carbon steel sheet of 0.015 wt% and thickness of 1 mm was used as a specimen. Both sides of each specimen sheet were ground and flattened until 0.05-0.80 mm by mechanical polishing finally using colloidal silica particles of 0.05 μm. The thickness variation of speci- men sheet was controlled within 5%. The back side was electroplated with a nickel layer of 0.5 μm in thickness by cathodic polarization at 0.1 A cm −2 in a Watt's bath (1 mol dm −3 NiSO4 + 0.2 mol dm −3 NiCl2 + 0.6 mol dm −3 H3BO3) at 323 K. Fig.1is a schematic diagram of a Devanathan-Stachurski cell used in this study. The specimen sheet was sandwiched between the two electrochemical cells made from acrylic glass with two O-rings and connected with two potentiostats as working electrodes. The front and back sides of the sample sheet served as hydrogen entry and exit electrodes, respectively. Each cell had a platinum counter electrode and an Ag/AgCl/saturated KCl reference electrode with a Luggin- Haber capillary. The electrolyte in both cells was pH 8.4 boric-borate buffer solution deaerated by bubbling pure Ar gas. The electrolyte in the hydrogen entry side cell was flowed by using a bimorph pump at a constant or sinusoidally pertubated volume flow rate in the range of 0.145-1.50 cm 3 s −1 , while the electrolyte in the cell for the hydrogen exit side was stagnant. During the potentiostatic polarization of entry and exit electrodes, currents flowing through both electrodes were recorded with the electrolyte flow rate using a PC controlled by a LabVIEW (National Instruments) program.\",\"PeriodicalId\":11470,\"journal\":{\"name\":\"ECS Electrochemistry Letters\",\"volume\":\"3 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1149/2.011406EEL\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ECS Electrochemistry Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1149/2.011406EEL\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ECS Electrochemistry Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1149/2.011406EEL","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5

摘要

实验用重量为0.015 wt%,厚度为1 mm的碳钢片作为试样。每个试样片的两面都经过机械抛光,打磨平整至0.05 ~ 0.80 mm,最后使用0.05 μm的硅胶胶体颗粒。规格板厚度变化控制在5%以内。在323 K的瓦特浴(1 mol dm−3 NiSO4 + 0.2 mol dm−3 NiCl2 + 0.6 mol dm−3 H3BO3)中,以0.1 a cm−2阴极极化,在背面镀上0.5 μm厚度的镍层。图1是本研究使用的Devanathan-Stachurski细胞示意图。样品片夹在两个由丙烯酸玻璃制成的电化学电池之间,用两个o形环连接两个电位器作为工作电极。样品片的正面和背面分别作为氢气的入口和出口电极。每个电池都有一个铂对电极和一个Ag/AgCl/饱和KCl参比电极,带一个lagin - Haber毛细管。两个电池的电解液均为pH为8.4的硼酸硼缓冲液,经鼓泡纯氩气除氧。氢气入口侧电池中的电解质通过双晶圆泵以恒定或正弦扰动体积流速在0.145 ~ 1.50 cm 3 s−1范围内流动,而氢气出口侧电池中的电解质则处于停滞状态。在输入电极和输出电极的恒电位极化过程中,用LabVIEW (National Instruments)程序控制的PC机记录通过两个电极的电流和电解质流速。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Convection-Dependent Hydrogen Permeation into a Carbon Steel Sheet
Experimental A carbon steel sheet of 0.015 wt% and thickness of 1 mm was used as a specimen. Both sides of each specimen sheet were ground and flattened until 0.05-0.80 mm by mechanical polishing finally using colloidal silica particles of 0.05 μm. The thickness variation of speci- men sheet was controlled within 5%. The back side was electroplated with a nickel layer of 0.5 μm in thickness by cathodic polarization at 0.1 A cm −2 in a Watt's bath (1 mol dm −3 NiSO4 + 0.2 mol dm −3 NiCl2 + 0.6 mol dm −3 H3BO3) at 323 K. Fig.1is a schematic diagram of a Devanathan-Stachurski cell used in this study. The specimen sheet was sandwiched between the two electrochemical cells made from acrylic glass with two O-rings and connected with two potentiostats as working electrodes. The front and back sides of the sample sheet served as hydrogen entry and exit electrodes, respectively. Each cell had a platinum counter electrode and an Ag/AgCl/saturated KCl reference electrode with a Luggin- Haber capillary. The electrolyte in both cells was pH 8.4 boric-borate buffer solution deaerated by bubbling pure Ar gas. The electrolyte in the hydrogen entry side cell was flowed by using a bimorph pump at a constant or sinusoidally pertubated volume flow rate in the range of 0.145-1.50 cm 3 s −1 , while the electrolyte in the cell for the hydrogen exit side was stagnant. During the potentiostatic polarization of entry and exit electrodes, currents flowing through both electrodes were recorded with the electrolyte flow rate using a PC controlled by a LabVIEW (National Instruments) program.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ECS Electrochemistry Letters
ECS Electrochemistry Letters ELECTROCHEMISTRY-MATERIALS SCIENCE, MULTIDISCIPLINARY
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信