Revealing the adsorption mechanism of copper on hemp-based materials through EDX, nano-CT, XPS, FTIR, Raman, and XANES characterization techniques

Chemical engineering journal advances(2022)

引用 13|浏览9
暂无评分
摘要
• Activated (SHI-C) and grafted (SHI-BTCA) hemp-based samples were used for recovery copper from solutions. • Microscopic and spectroscopic techniques permit to distinguish the type of interactions involved in the phenomena • Various adsorption mechanisms for copper were discussed. • The main adsorption mechanism was surface adsorption and diffusion for SHI-C and ion-exchange and precipitation for SHI-BTCA. Hemp-based materials have been recently proposed as adsorbents for metals present in aqueous solutions using adsorption-oriented processes. This study aims to reveal the adsorption mechanism of materials prepared from hemp shives as co-products of the hemp industry, namely sodium carbonate-activated (SHI-C) and polycarboxylic agent-grafted (SHI-BTCA) hemp shives. The interactions between copper and two hemp-based materials were characterized by different microscopic and spectroscopic techniques such as energy-disperse X-ray (EDX) spectroscopy, computed nano-tomography (nano-CT), X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared (FTIR) spectroscopy, Raman spectroscopy, and X-ray absorption near-edge structure (XANES) spectroscopy. The results showed remarkable different mechanisms for copper adsorption onto the SHI-C and SHI-BTCA hemp shives. Namely, copper surface adsorption and diffusion in the structure of the SHI-C material were predominant, whereas the adsorption of copper onto SHI-BTCA was due to a chemisorption phenomenon and ion-exchange involving the adsorbent carboxylate groups. The combination of the abovementioned complementary microscopic and spectroscopic techniques allowed us to characterize and distinguish the type of interactions involved in the liquid-solid adsorption phenomena.
更多
查看译文
关键词
Hemp shives,Copper,Adsorption,Mechanism
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要