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化学改性表面变电荷氧化煅烧底物对 Pb(II)离子的吸附。

Adsorption of Pb (II) ions on variable charge oxidic calcined substrates with chemically modified surface.

机构信息

Escuela de Ingeniería Química, Facultad de Ingeniería, Universidad de Los Andes, Mérida, 5101, Venezuela.

Grupo de Investigación Estudios Interdisciplinarios, Ingeniería Ambiental, Facultad de Ingeniería, Universidad Nacional de Chimborazo, Riobamba, Chimborazo Province, 060103, Ecuador.

出版信息

F1000Res. 2024 Mar 28;12:747. doi: 10.12688/f1000research.132880.2. eCollection 2023.

Abstract

BACKGROUND

The paper describes lead ion adsorption on variable charge oxidic calcined substrates with chemically modified surfaces. Amphoteric oxides of iron, aluminum, titanium, and manganese, change their surface electric charge after acid or alkaline treatment, letting cationic or anionic adsorption reactions from aqueous solutions. This property allows using them as adsorbing substrate for heavy metals retention in water treatment systems.

METHODS

Substrate was prepared by extruding cylindrical strips from a saturate paste of the oxidic lithological material-OLM; dries it up and thermally treated by calcination. The study was performed by triplicated trial, on batch mode, using 2 grams samples of treated with NaOH 0.1N and non-treated substrate. Lead analysis was performed by AAS-GF. Freundlich and Langmuir models were used to fit results. Comparing differential behavior between treated and non-treated substrates showed the variable charge nature of the OLM.

RESULTS

Results show -type isotherms for the adsorption of Pb(II) ions on the activated substrate, suggesting good affinity between Pb(II) ions and OLM's surface. Average value of adsorption capacity ( ) for activated substrate (1791.73±13.06), is around four times greater than the non-activated substrate (491.54±31.97), during the adsorption reaction, 0.35 and 0.26 mmolH of proton are produced on the activated and non-activated substrate respectively using a 1 M Pb(II) solution and 72.2 and 15.6 mmolH using a 10 M Pb(II) solution. This acidification agrees with the theoretic model of transitional metals chemisorption on amphoteric oxides, present in lithological material used for the preparation of adsorbent substrates, confirming the information given by the -type isotherms.

CONCLUSIONS

Results suggest that these variable charge oxidic adsorbent substrate show great potential as an alternative technique for water treatment at small and medium scale using granular filtration system. The easiness and low price make them suitable to apply in rural media where no treating water systems is available.

摘要

背景

本文描述了带化学改性表面的变电荷氧化煅烧基底上铅离子的吸附。铁、铝、钛和锰的两性氧化物在酸或碱处理后会改变其表面电荷,从而使阳离子或阴离子吸附反应从水溶液中发生。这种特性使其可用作重金属在水处理系统中的保留的吸附基质。

方法

用氧化岩性材料-OLM 的饱和糊状物挤出圆柱形条带制备基质;将其干燥并进行热煅烧处理。该研究采用重复三批试验,在分批模式下,使用 2 克经 NaOH 0.1N 处理和未经处理的基质样品进行。使用原子吸收光谱法(AAS-GF)进行铅分析。采用 Freundlich 和 Langmuir 模型拟合结果。比较处理和未处理的基质之间的差异行为表明了 OLM 的变电荷性质。

结果

结果表明,在活化基质上吸附 Pb(II)离子的吸附等温线呈 - 型,表明 Pb(II)离子与 OLM 表面之间具有良好的亲和力。活化基质的平均吸附容量( )为 1791.73±13.06,约为非活化基质(491.54±31.97)的四倍,在吸附反应中,使用 1 M Pb(II)溶液时,在活化和非活化基质上分别产生 0.35 和 0.26 mmolH 的质子,使用 10 M Pb(II)溶液时,分别产生 72.2 和 15.6 mmolH 的质子。这种酸化与两性氧化物上过渡金属化学吸附的理论模型一致,这种两性氧化物存在于用于制备吸附剂基质的岩性材料中,证实了 - 型等温线所提供的信息。

结论

结果表明,这些变电荷氧化吸附剂基质作为小型和中型规模水处理的替代技术具有很大的潜力,使用颗粒过滤系统。其简便性和低廉的价格使它们适合在没有处理水系统的农村地区应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dee/10989276/4f3ec43a7a9a/f1000research-12-163125-g0000.jpg

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