吸附
粒径
化学
扩散
水溶液中的金属离子
金属
离子
粒子(生态学)
航程(航空)
无机化学
分析化学(期刊)
色谱法
材料科学
物理化学
热力学
有机化学
地质学
物理
复合材料
海洋学
作者
Elizabeth H. Gora,Samuel G. Saldana,Lauren M. Casper,Victor Coll Sijercic,Olga A. Giza,Rebecca L. Sanders
出处
期刊:ACS omega
[American Chemical Society]
日期:2022-10-17
卷期号:7 (43): 38600-38612
被引量:8
标识
DOI:10.1021/acsomega.2c04058
摘要
Spent coffee grounds (SCGs) are common waste products that can be used as low-cost adsorbents to remove contaminants from water. SCGs come in a range of particle sizes based on how they were ground to brew coffee. However, few studies have investigated how SCG particle size influences the adsorption rate and capacities of metal ions. In this study, SCGs were washed under alkaline conditions, creating exhausted coffee grounds (ECGs). ECGs were sieved into four particle size ranges (106-300, 300-500, 500-710, and 710-1000 μm). Monocomponent batch adsorption experiments were conducted with each size fraction using 0.3 mM Pb2+, Cu2+, Zn2+, and Ni2+ at pH 5.5 to examine the effect of particle size on the adsorption rates and capacities. The initial adsorption rates for all the four metal ions were 8-12 times higher for the smallest ECGs compared to the largest ECGs. Slower initial adsorption rates with increasing particle size were due to intraparticle diffusion of metal ions into the porous structure of ECGs. However, the equilibrium adsorption capacities for each metal ion and the surface acidic group concentrations were similar across the range of particle sizes studied, suggesting that grinding ECGs does not substantially change the number of adsorption sites. The equilibrium adsorption capacities for Cu2+ and Pb2+ were 0.18 and 0.17 mmol g-1, respectively. Zn2+ and Ni2+ had lower adsorption capacities of 0.12 and 0.10 mmol g-1, respectively. The time needed to reach equilibrium ranged from less than 2 h for Zn2+ and Ni2+ adsorption onto the smallest ECGs to several hours for Pb2+ or Cu2+ adsorption onto the largest ECGs. Future adsorption studies should consider the effect of ECG particle size on reported adsorption capacities, particularly for shorter experiments that have not yet reached equilibrium.
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