Enhanced continuous adsorption of silver ions using graphite oxide impregnated with zeolite LTA under high pressure and temperature conditions

IF 5.2 2区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Molecular Liquids Pub Date : 2025-05-15 Epub Date: 2025-03-12 DOI:10.1016/j.molliq.2025.127380
Gabriel D. Reske , Hercules A. Pereira , Guilherme L. Dotto , Fernanda De Castilhos
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Abstract

This study explores the potential of zeolite-impregnated graphite oxide (GOIZ) as a highly efficient adsorbent for the continuous removal of silver ions (Ag(I)) under elevated temperature and pressure conditions in a fixed-bed column. Adsorption performance significantly improved at higher temperatures (100–200 °C), with the best results obtained at 200 °C and 25 MPa. Under these conditions, the maximum stoichiometric adsorption capacity reached 407 mg/g, a substantial increase compared to 47 mg/g under normal conditions (25 °C and 0.101 MPa). This improvement is attributed to enhanced activation of adsorption sites, reduced mass transfer resistance, and progressive desolvation of Ag(I) ions under elevated temperatures, as well as liquid compression effects at high pressure. Interestingly, only at 200 °C and 25 MPa pressure did play a synergistic role, likely due to conditions approaching the subcritical state of water, altering the interaction between adsorbent and adsorbate. Mathematical modeling using the Dose-Response model demonstrated superior predictive accuracy (R2 ≥ 0.954) compared to the Thomas model, accurately describing Ag(I) adsorption behavior under varying experimental conditions. Mechanistic analysis revealed a adsorption process governed by redox reactions, where Ag+ ions were reduced to Ag0 on the adsorbent surface, electrostatic interactions between Ag+ ions and the negatively charged functional groups of GOIZ and cationic-exchange. The formation of Ag0 on the adsorbent surface was confirmed, with further adsorption hindered by the resulting silver layer. These findings underscore the exceptional capability of GOIZ for Ag(I) removal in wastewater treatment, particularly under extreme temperature and pressure conditions.
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在高压和高温条件下使用浸渍了沸石 LTA 的氧化石墨增强银离子的连续吸附能力
本研究探索了沸石浸渍氧化石墨(GOIZ)作为一种高效吸附剂的潜力,在固定床柱的高温高压条件下连续去除银离子(Ag(I))。在较高温度下(100-200℃)吸附性能显著提高,在200℃、25 MPa条件下吸附效果最好。在此条件下,最大化学计量吸附量达到407 mg/g,比正常条件下(25°C, 0.101 MPa)的47 mg/g有显著提高。这种改善是由于吸附位点的活化增强,传质阻力降低,Ag(I)离子在高温下逐渐溶解,以及高压下的液体压缩效应。有趣的是,只有在200°C和25 MPa压力下才发挥协同作用,可能是由于条件接近水的亚临界状态,改变了吸附剂和吸附物之间的相互作用。与Thomas模型相比,使用剂量响应模型建立的数学模型具有更高的预测精度(R2≥0.954),可以准确地描述不同实验条件下Ag(I)的吸附行为。吸附机理分析表明,吸附过程受氧化还原反应、Ag+离子与GOIZ负电荷官能团的静电相互作用和阳离子交换等控制。在吸附剂表面证实了Ag0的形成,所产生的银层阻碍了进一步的吸附。这些发现强调了GOIZ在废水处理中去除Ag(I)的卓越能力,特别是在极端温度和压力条件下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Molecular Liquids
Journal of Molecular Liquids 化学-物理:原子、分子和化学物理
CiteScore
10.30
自引率
16.70%
发文量
2597
审稿时长
78 days
期刊介绍: The journal includes papers in the following areas: – Simple organic liquids and mixtures – Ionic liquids – Surfactant solutions (including micelles and vesicles) and liquid interfaces – Colloidal solutions and nanoparticles – Thermotropic and lyotropic liquid crystals – Ferrofluids – Water, aqueous solutions and other hydrogen-bonded liquids – Lubricants, polymer solutions and melts – Molten metals and salts – Phase transitions and critical phenomena in liquids and confined fluids – Self assembly in complex liquids.– Biomolecules in solution The emphasis is on the molecular (or microscopic) understanding of particular liquids or liquid systems, especially concerning structure, dynamics and intermolecular forces. The experimental techniques used may include: – Conventional spectroscopy (mid-IR and far-IR, Raman, NMR, etc.) – Non-linear optics and time resolved spectroscopy (psec, fsec, asec, ISRS, etc.) – Light scattering (Rayleigh, Brillouin, PCS, etc.) – Dielectric relaxation – X-ray and neutron scattering and diffraction. Experimental studies, computer simulations (MD or MC) and analytical theory will be considered for publication; papers just reporting experimental results that do not contribute to the understanding of the fundamentals of molecular and ionic liquids will not be accepted. Only papers of a non-routine nature and advancing the field will be considered for publication.
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