Elmekawy Ahmed, Quach Qui, Abdel-Fattah Tarek M
Department of Physics, Tanta University, Tanta 31527, Egypt.
Applied Research Center, Thomas Jefferson National Accelerator Facility, Department of Molecular Biology and Chemistry, Christopher Newport University, Newport News, VA 23606, USA.
Nanomaterials (Basel). 2024 Jul 3;14(13):1143. doi: 10.3390/nano14131143.
In aquatic environments, the presence of iodine species, including radioactive isotopes like I and I, poses significant environmental and health concerns. Iodine can enter water resources from various sources, including nuclear accidents, medical procedures, and natural occurrences. To address this issue, the use of natural occurring nanoporous minerals, such as zeolitic materials, for iodine removal will be explored. This study focuses on the adsorption of iodine by silver-modified zeolites (13X-Ag, 5A-Ag, Chabazite-Ag, and Clinoptilolite-Ag) and evaluates their performance under different conditions. All materials were characterized using scanning electron microscopey (SEM), energy-dispersive X-ray spectroscopy (EDS), powdered X-ray diffraction (P-XRD), Fourier-transform infrared spectrometry (FTIR), and nitrogen adsorption studies. The results indicate that Chabazite-Ag exhibited the highest iodine adsorption capacity, with an impressive 769 mg/g, making it a viable option for iodine removal applications. 13X-Ag and 5A-Ag also demonstrated substantial adsorption capacities of 714 mg/g and 556 mg/g, respectively, though their behavior varied according to different models. In contrast, Clinoptilolite-Ag exhibited strong pH-dependent behavior, rendering it less suitable for neutral to slightly acidic conditions. Furthermore, this study explored the impact of ionic strength on iodine adsorption, revealing that Chabazite-Ag is efficient in low-salinity environments with an iodine adsorption capacity of 51.80 mg/g but less effective in saline conditions. 5A-Ag proved to be a versatile option for various water treatments, maintaining its iodine adsorption capacity across different salinity levels. In contrast, Clinoptilolite-Ag exhibited high sensitivity to ionic competition, virtually losing its iodine adsorption ability at a NaCl concentration of 0.1 M. Kinetic studies indicated that the pseudo-second-order model best describes the adsorption process, suggesting chemisorption mechanisms dominate iodine removal. Chabazite-Ag exhibited the highest initial adsorption rate with a k value of 0.002 mg g h, emphasizing its superior adsorption capabilities. Chabazite and Clinoptilolite, naturally occurring minerals, provide eco-friendly solutions for iodine adsorption. Chabazite superior iodine removal highlights its value in critical applications and its potential for addressing pressing environmental challenges.
在水生环境中,包括碘-129和碘-131等放射性同位素在内的碘物种的存在,引发了重大的环境和健康问题。碘可从包括核事故、医疗程序和自然现象在内的各种来源进入水资源。为解决这一问题,将探索使用天然存在的纳米多孔矿物,如沸石材料,来去除碘。本研究聚焦于银改性沸石(13X-Ag、5A-Ag、菱沸石-Ag和斜发沸石-Ag)对碘的吸附,并评估它们在不同条件下的性能。所有材料均使用扫描电子显微镜(SEM)、能量色散X射线光谱仪(EDS)、粉末X射线衍射仪(P-XRD)、傅里叶变换红外光谱仪(FTIR)和氮气吸附研究进行了表征。结果表明,菱沸石-Ag表现出最高的碘吸附容量,达到了令人印象深刻的769 mg/g,使其成为碘去除应用的可行选择。13X-Ag和5A-Ag也分别表现出714 mg/g和556 mg/g的显著吸附容量,不过它们的行为根据不同模型有所不同。相比之下,斜发沸石-Ag表现出强烈的pH依赖性,使其不太适合中性至微酸性条件。此外,本研究还探讨了离子强度对碘吸附的影响,结果表明,菱沸石-Ag在低盐度环境中效率较高,碘吸附容量为51.80 mg/g,但在含盐条件下效果较差。5A-Ag被证明是各种水处理的通用选择,在不同盐度水平下均能保持其碘吸附容量。相比之下,斜发沸石-Ag对离子竞争表现出高度敏感性,在NaCl浓度为0.1 M时几乎失去其碘吸附能力。动力学研究表明,准二级模型最能描述吸附过程,这表明化学吸附机制主导了碘的去除。菱沸石-Ag表现出最高的初始吸附速率,k值为0.002 mg g-1 h-1,突出了其卓越的吸附能力。菱沸石和斜发沸石这两种天然存在的矿物,为碘吸附提供了环保解决方案。菱沸石卓越的碘去除能力凸显了其在关键应用中的价值以及应对紧迫环境挑战的潜力。