从糠醛中合成2-((呋喃-2-基)亚甲基)-1-苯腙玉米分离结果及其在锌金属中的缓蚀剂应用

H. Sihotang
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引用次数: 0

摘要

以玉米芯分离得到的糠醛基团与苯肼缩合为原料,合成了2-((呋喃-2-基)亚甲基-1-苯腙。糠醛与苯肼在乙醇溶剂中回流反应1小时。将9.6 g (0.1 mol)糠醛与5.4 g (0.05 mol)苯肼缩合,得到10.54 g(67.02%)苯腙,并通过红外光谱分析,发现在1597 cm-1附近存在振动C = N。fenilhidra酮的抑制率为78.47%,而糠醛的抑制率为58.18%,苯肼的抑制率为50.04%。苯腙的抑制率为78.47%,糠醛和苯肼的抑制率分别为58.18%和50.04%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis 2-((Furan-2-yl) Methylene)-1-Phenilhydrazone from Furfural Results of Corn Isolation and Its Utilization as Corrosion Inhibitor in Zinc (Zn) Metal
Synthesis of 2-((furan-2-yl) methylene)-1-phenylhydrazone has been carried out by reaction of condensation of furfural aldehyde groups obtained from the isolation of corn cobs with phenylhydrazine. Furfural condensation with phenylhydrazine was carried out by refluxing in ethanol solvent for 1 hour. Of the 9.6 g (0.1 mol) furfural which was condensed with 5.4 g (0.05 mol) phenylhydrazine obtained yield of 10.54 g (67.02%) phenylhydrazone which was then analyzed by FT-IR spectroscopy showing the presence of vibration C = N in the area around 1597 cm-1. Fenilhidrazone was tested for inhibitor with 78.47% and compared with furfural as much as 58.18%, and phenylhydrazine as much as 50.04%. The results obtained by phenylhydrazone were more efficient at inhibiting the results of 78.47% while furfural and phenylhydrazine were only 58.18% and 50.04%.
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