Preparation and NH4+ Adsorption Performance of Ultrafine Lignite-Based Porous Materials

Abstract

This study aimed to increase the ammonium nitrogen adsorption capacity of lignite using ultrafine grinding, aiming to reduce eutrophication in water bodies. Ammonium sulfate (NH4)2SO4 was employed as a stand-in for ammonium nitrogen in water solutions. The lignite sample for adsorption was processed with varying milling times. Adsorption efficacy was assessed primarily through isothermal adsorption tests and other techniques. Additionally, the study delved into the adsorption mechanisms. The results demonstrate that lignite ground for 50 min follows monolayer adsorption, characterized by minimal pore size and reduced diffusion rates, thereby extending the time to reach equilibrium and maximizing adsorption. BET and SEM analyses show that coal powder is effectively ground by zirconia balls in a vertical stirring mill, diminishing its particle size and forming new micropores. Concurrently, larger native pores are transformed into mesopores and micropores, providing numerous sites for NH4+ adsorption. XPS and FTIR analyses indicate an increase in exposed carbonaceous surfaces and oxygen-containing functional groups in ultrafine lignite. Ammonium ions replace hydrogen in carboxyl groups to form COONH4, and hydrogen bonds may form between NH4+ and C-O groups. Additionally, the electrostatic attraction between NH4+ and the coal surface further enhances adsorption. It can be concluded that the physical grinding process increases the specific surface area and creates more active adsorption sites, which in turn, boosts NH4+ adsorption capacity. The maximum equilibrium adsorption capacity is as high as 550 mg/g. This study suggests that ultrafine lignite is a promising material for treating ammonia-nitrogen wastewater.