首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Gravimetric,electrochemical, and morphological studies of an isoxazole derivative as corrosion inhibitor for mild steel in 1M HCl
Institution:1. Department of Chemistry, College of Science, Yanbu-30799, Taibah University, Al-Madina, Saudi Arabia;2. Corrosion Research Laboratory, Department of Applied Chemistry, Faculty of Engineering and Technology, Aligarh Muslim University, Aligarh 202002, India;3. Department of Chemistry, Faculty of Science, Aligarh Muslim University, Aligarh 202002, India;4. Department of Chemistry and Environmental Science, New Jersey Institute of Technology, Newark, NJ 07102, USA
Abstract:In present study, an isoxazole derivative, namely, (Z)-4-(4-hydroxy-3-methoxybenzylidene)-3-methylisoxazol-5(4H)-one referred here as (IOD) has been studied as an environment-friendly corrosion inhibitor for mild steel (MS) in acidic medium (1 M HCl). The present work was investigated by gravimetric, electrochemical impedance spectroscopy (EIS), potentiodynamic polarization (PDP), fourier-transform infrared (FT-IR) spectroscopy techniques. Atomic force microscopy (AFM), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS) confirmed the surface morphologies of the MS surface with and without IOD in the acid medium. The inhibition efficiency (I.E.) of IOD was increased by rising its concentration attaining maximum value (96.6%) at 300 ppm at 30 °C and decreases with increasing temperature from 30 °C to 60 °C. The adsorption of studied inhibitor followed Langmuir adsorption isotherm model. The PDP study revealed that the IOD acts as a mixed-type inhibitor with predominating anodic effect. The EIS study confirmed that increasing IOD concentration enhances the charge transfer resistance (Rct) and then reduces the double layer capacitance (Cdl) owing to the development of a protective layer on the MS surface.
Keywords:Metal corrosion  Acid inhibition  Eco-friendly compound  Mix-type inhibitor  Electrochemical study
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号