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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2025 · IF 5.4

Synergistic Optimization of Pb(II) Adsorption from Aqueous Solutions by Manganese-Doped Carbon Aerogels

Sheng Cai,Yirong Zhang,Zhi ming Liu,Luming Tian,Deliang He,Ruirui Zhu,Yan Xing

In this study, a novel carbon aerogel adsorbent (Mn-PA-CS) was synthesized through a one-step calcination-activation method using manganese acetate as the precursor. Unlike conventional phytic acid-activated carbons, this work introduces manganese doping as an effective strategy to tailor the pore structure and surface chemistry. The resulting material features enriched surface P/O functional groups and a significantly increased proportion of micropores (0.7–0.8   nm), which closely match the hydration diameter of Pb(II) ions, alongside elevated defect density (ID/IG = 0.94). These modifications synergistically promote adsorption through micropore filling, electrostatic attraction, and surface complexation. The optimized Mn-PA-CS, prepared with 100   mg of manganese acetate, exhibited a high Pb(II) uptake capacity of 302.88   mg·g -1 , which represents a 132.43% improvement compared to the undoped material. The adsorption behavior followed pseudo-second-order kinetics and the Freundlich isotherm, suggesting a spontaneous, endothermic, and multilayer chemisorption process. This study indicates that transition metal doping is a promising strategy for regulating the adsorption performance of bio-derived carbon materials.

研究领域: 环境科学 · 材料科学 · 化学工程 · 水处理技术
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ACS Applied Materials & Interfaces · 2024 · IF 8.3

Defect-Engineered MOF-801/Sodium Alginate Aerogel Beads for Boosting Adsorption of Pb(II)

Mengshuo Du,Yingying Wang,Youyu Cao,Wenzhi Tang,Zhonghong Li

Metal–organic frameworks (MOFs) are attractive adsorbents for heavy metal capture due to their superior stability, easy modification, and adjustable pore size. However, their inherent microporous structure poses challenges in achieving a higher adsorption capacity. Defect engineering is considered a simple method to create hierarchical MOFs with larger pores. Here, we employed l-aspartic acid as a mixed linker to bind Zr4+ clusters in competition with fumaric acid of MOF-801 to create defects, and the pore size was increased from 4.66 to 15.65 nm. Mercaptosuccinic acid was subsequently used as a postexchange ligand to graft the resultant MOF-801 by acid-ammonia condensation to further expand the pore size to 22.73 nm. Notably, the −NH2, −COOH, and −SH groups contributed by these two ligands increased the adsorption sites for Pb(II). The obtained defective MOF-801 with larger pores was thereafter loaded onto sodium alginate to form aerogel beads as adsorbents, and an adsorption capacity of 375.48 mg/g for Pb(II) was achieved, which is ∼51 times that of pristine MOF-801. The aerogel beads also exhibited outstanding reusability with a removal efficiency of ∼90.23% after 5 cycles of use. The adsorption mechanism of Pb(II) included ion-exchange interaction, as well as chelation interactions of Pb–O, Pb–NH2, and Pb–S. The versatile combination of defect engineering and composite beads provides novel inspirations for MOF modification for boosting heavy metal adsorption.

研究领域: 材料科学 · 环境科学 · 化学工程
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Engineered Multi-Shelled hollow mesoporous organosilica for efficient Pb(II) and Cr(VI) removal

Meng Cheng,Yuqi Liu,Hao Jiang,Chunling Li,Shuangqing Sun,Songqing Hu

Adsorbents with fast kinetics and high capacity have always been attractive for wastewater treatment. Herein, multi-shelled hollow mesoporous organosilica functionalized by hydroxyphosphatoethyl groups on dual-pore surfaces (P-HMO) is prepared by general one-pot co-condensation. The resulting P-HMO exhibits high hydrophilicity, large surface area and well-developed pore structure, providing P-HMO fast adsorption kinetics (C 0  = 320 mg·L -1 , equilibrium within 5 min) and ultrahigh adsorption efficiency for Pb(II) and Cr(VI), the adsorption capacity reaches 1056.53 and 869.56 mg·g −1 , respectively. Furthermore, P-HMO displays outstanding reusability over 10 adsorption–desorption cycles thanks to the stable framework structure that can resist wear and tear during water treatment. The advantages of long service life, high efficiency and broad pH range make P-HMO promising in industrial water purification.

CAS / MDL: 1336-21-6 57-09-0
研究领域: 环境科学 · 材料科学
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CERAMICS INTERNATIONAL · 2025 · IF 5.6

Adsorption behavior and mechanism of MB, Pb(II) and Cu(II) on porous geopolymers

Yi Fang,Lang Yang,Feng Rao,Yongming Zheng,Zhenguo Song

In this study, a low-cost porous geopolymers (PGP) were prepared using coal gangue and fly ash as raw materials to remove organic and heavy metal ions from wastewater. Various characterization techniques were employed to investigate the microstructure, morphology, pore size distribution, and surface functional groups of the porous geopolymers. The results indicate that the geopolymer exhibits a porous structure with hydroxyl groups on the surface after foaming. It was found that the porous geopolymers exhibited good adsorption capacity for Methylene Blue (MB), Cu(II), and Pb(II), with optimal adsorption capacities reaching 35.60 mg/g, 98.31 mg/g, and 85.67 mg/g, respectively. Fitting analysis suggests that the adsorption of MB, Cu(II), and Pb(II) is better described by the pseudo-second-order kinetic model and the Freundlich isotherm model. This indicates that the adsorption process is primarily chemical adsorption with multilayer adsorption. Competitive adsorption studies showed that Cu(II) could enhance the adsorption of MB, while Pb(II) had no significant effect on the adsorption of MB. Mechanistic studies revealed that the adsorption of MB by PGP is mainly through pore adsorption, electrostatic attraction, and hydrogen bond formation; whereas the adsorption of Cu(II) and Pb(II) is primarily through pore adsorption, electrostatic attraction, chemical reactions, and ion exchange. Recycling experiments demonstrated that after five repetitions, the adsorption capacity of PGP for the three pollutants remained above 60 %. These findings confirm the potential of porous geopolymers as adsorbents. Preliminary cost analysis shows that the adsorption cost of porous geopolymers is only 2.07 RMB/kg, making the geopolymer adsorbent economically advantageous and promising for application, especially considering its ability to utilize industrial solid waste.

CAS / MDL: 7722-84-1
研究领域: 环境科学 · 材料科学
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MICROPOROUS AND MESOPOROUS MATERIALS · 2024 · IF 4.8

Optimization of zeolite ETS-10 synthesis for enhanced Pb(II) adsorption from aqueous solutions

Van-Hien Pham,Bich-Ngoc Duong,Duy-Khoi Nguyen,Loc Ton-That,N.T. Dang,D. Thanh Khan,Ngoc-Quyen Tran,Ngoc Duy Nguyen,Van-Phuc Dinh

The synthesis of zeolite ETS-10 is strongly influenced by factors such as pH, the amount of the structure-directing agent, hydrothermal temperature and duration, which collectively affect the material’s morphology and structure. This study thoroughly investigates the effects of these parameters on the synthesis of ETS-10 zeolite using TiCl 3 and a waterglass solution. Characterization of the materials was performed through X-ray diffraction (XRD), scanning electron microscopy (SEM), infrared spectroscopy (FT-IR), and nitrogen isotherm adsorption-desorption at 77 K (BET-BJH) techniques. The findings indicate that pH and the structure-directing agent significantly influenced the phase composition , while hydrothermal temperature predominantly determined the crystallization rate of ETS-10. Optimal synthesis conditions were established at an initial pH of 11, employing 0.3 g of the structure-directing agent and conducting hydrothermal crystallization at 230 °C for 24 h. Under these conditions, the ETS-10 zeolite produced exhibited a high surface area of 300.1 m 2 /g, making it effective in removing Pb 2+ ions from solution. In particular, when tested under optimal conditions (pH 5) for 600 min, Pb (II) adsorption by ETS-10 reached a maximum uptake capacity of 956.19 mg/g, as determined by the Langmuir isotherm model. This capacity surpasses that of as-synthesized ETS-10 prepared from alternative Ti sources and other materials used in previous studies on Pb(II) adsorption.

CAS / MDL: 7705-07-9
研究领域: 环境科学 · 材料科学
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Desalination and Water Treatment · 2024 · IF 1

Adsorption of Cd(II) and Pb(II) on biochars derived from grape vine shoots

Hui-yong Li,Deng-hui Yao,Qiu-ju Feng,Hai-bo Zeng,Jian-mei Liang,Zhi Zhou,Yun Tian,Nan Zhou,Xiang-yang Lu

Grape vine shoots were utilized as the biomass feedstock and pyrolyzed under temperatures ranging in 300°C–600°C with nitrogen atmosphere to produce biochars. The surface properties of the as-obtained biochars were characterized, followed with the careful investigation of the adsorption of lead and cadmium removal in aqueous environments. All as-prepared biochars had weak alkali characteristics and large amount of mineral species, which can greatly improve the adsorption performance. Outstanding storing capacities of 250.81, 327.31, 377.36 mg g –1 for Cd 2+ and 156.12, 237.25, 258.86 mg g –1 for Pb 2+ were exhibited by biochar pyrolyzed under 300°C, 450°C and 600°C, respectively. The adsorption equilibrium could be reached about 7 h and the suitable solution pH should be above 3. Both Langmuir and Freundlich models fitted the data well and precipitation was found to be the dominant mechanism for the adsorption of both metals. Overall, grape vine shoots are confirmed to be a promising feedstock to produce biochar sorbents of heavy metals in wastewater with excellent performance, economic cost, and easy process.

研究领域: 环境科学 · 材料科学 · 化学工程 · 污染控制
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2021 · IF 6.953

Ninhydrin-functionalized chitosan for selective removal of Pb(II) ions: Characterization and adsorption performance

Yingbi Chen,Jiali Tang,Shixing Wang,Libo Zhang

A chitosan-based adsorbents (CS-Ninhydrin) was prepared by grafting ninhydrin for Pb(II) ions adsorption. SEM-EDS, XRD and FTIR analysis were used to characterize the synthesized CS-Ninhydrin. The static adsorption experiments showed that CS-Ninhydrin had a good removal rate for Pb(II) ions in a wide range of pH 3 to 7, quickly reached equilibrium (120 min) and had a higher adsorption capacity (196 mg/g). Pseudo second-order and Langmuir models showed that the adsorption process of Pb(II) by CS-Ninhydrin was a single-layer chemical adsorption. Temperature experiments showed that the reaction was a spontaneous exothermic process. In the wastewater experiment, CS-Ninhydrin showed an excellent selectivity to Pb(II) ions. The reusability of CS-Ninhydrin was perfect after five adsorption-desorption cycles. The main adsorption mechanism was the chelating and electrostatic action between N and O groups in CS-Ninhydrin and Pb(II) ions. Therefore, the new adsorbent CS-Ninhydrin was expected to promote the wide application of chitosan in Pb(II) adsorption.

CAS / MDL: 485-47-2
研究领域: 环境科学 · 材料科学 · 化学工程
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MICROCHEMICAL JOURNAL · 2021 · IF 4.821

Indium-doped mesoporous Bi2S3-based electrochemical interface for highly sensitive detection of Pb(II)

Shiqi Wang,Jinrui Li,Yanqiu Fu,Zhongxin Zhuang,Zhonggang Liu

As a global toxic pollutant, lead (Pb(II)) causes serious risks for living organism and the environment, it is thus of critical importance to explore a facile and efficient sensing protocol for the detection of Pb(II). Herein, we proposed the flower-like In-doped Bi 2 S 3 (IDB) with mesoporous nanostructure as an electrochemical sensing interface for the Pb(II) detection, which was synthesized via a facile solvothermal method. The fabricated IDB/GCE exhibited a high sensitivity of 78.1 μA·μM −1 and a satisfied detection limit (LOD) as 0.017 μΜ with robust stability and remarkable anti-interference capability. Plausible mechanism of electrochemical sensing of Pb(II) was proposed based on electrochemical and characterization results, where the mesoporous IDB could provide numerous electrocatalytic active sites, and efficiently accumulate target Pb(II) onto the electrode surface, leading to the improved electrochemical performance. Besides, the complex state of Pb(II) was analyzed with IDB/GCE, and a tentative reference on the detection of complex state of Pb(II) was achieved with the favorable results. Furthermore, the fabricated IDB/GCE could be applied for the analysis of Pb(II) in real water sample with high reliability.

CAS / MDL: 10035-06-0
研究领域: 环境科学 · 分析化学 · 材料科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2020 · IF 5.774

Enhanced removal of Pb(II) and organics by titanate in a designed simultaneous process

Jingtao Bi,Jingkang Wang,Xin Huang,Qingqing Tao,Miao Chen,Ting Wang,Hongxun Hao

As a superior cation-exchanger and photocatalyst, titanate exhibited efficient ability for heavy metals decontamination and organics degradation. However, no reports about simultaneous removal of heavy metals and organics by using titanate has been found. The influence of intercalated heavy metal on the photocatalytic performances of titanate and its mechanism was poorly understood. In this work, titanate materials with different amounts of intercalated Pb(II) were prepared. Analytical TEM mapping images showed the uniform distributions of intercalated Pb(II) in titanate, excluding the formation of segregated nano-domains comprising either titanate or Pb-titanate. The crystalline and luminescent properties, which are relevant with the specific surface area and migration/recombination of the charge carriers, were considered as critical factors influencing the photocatalytic performance since the surficial charge states and derived band structures of titanate with different amounts of Pb(II) were almost identical. Steady state reaction experiments revealed that the catalytic activity of titanate after Pb(II) intercalation first sharply increased for 0.10Pb-Titanate and then decreased with further Pb(II) insertion. Better catalytic performance of 0.10Pb-Titanate was attribute to larger specific surface area, superior sorption affinity, higher excited charge carrier’s quantity and satisfied luminescence lifetime. Finally, it was observed that simultaneous removal strategy by pure titanate not only enhanced the sorption of lead ions than individual removal system but also promoted the photocatalytic ability than 0.10Pb-Titanate, which provides a new idea for the utilization and optimization of titanate materials for simultaneous decontamination of heavy metals and organics.

CAS / MDL: 13463-67-7
研究领域: 环境科学 · 材料科学
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2019 · IF 4.784

Adsorption of Pb(II) from aqueous solution by polyacrylic acid grafted magnetic chitosan nanocomposite

Dalin Hu,Zhenwei Lian,Hongyi Xian,Ran Jiang,Nan Wang,Yingying Weng,Xiaowu Peng,Sanming Wang,Xiao–Kun Ouyang

A creative combination of chitosan with polyacrylic acid (PAA) improves the acidity resistance of chitosan and increases its potential in the field of adsorption. In order to facilitate recovery, magnetic nanoparticles were incorporated in CS–PAA to obtain a magnetic-CS–PAA (MCS–PAA) nanocomposite. The physical and chemical characteristics of the composite adsorbent MCS–PAA were determined by SEM, TEM, FTIR, EDX , XRD, and XPS. This environmental-friendly, magnetic, composite adsorbent showed significantly better adsorption performance than those of the individual adsorbents alone. The maximal adsorption capacity was 204.89 mg/g according to the Langmuir isotherm model, when the concentration of Pb(II) was 100 mg/L at the equilibrium time of 70 min. The main adsorption mechanism was the complexation between the carboxyl, amino, and hydroxyl groups in MCS–PAA and Pb(II). Further, introduction of PAA also improved the acid resistance of CS. The new adsorbent MCS–PAA is thus expected to facilitate a wider range of applications for chitosan in the adsorption of Pb(II).

研究领域: 环境科学 · 材料科学
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ACS Omega · 2019 · IF 2.584

Synthesis of Amino-Functionalized Waste Wood Flour Adsorbent for High-Capacity Pb(II) Adsorption

Yi Tan,Kaili Wang,Qian Yan,Shifeng Zhang,Jianzhang Li,Yong Ji

An innovative wood flour-based adsorbent for Pb(II) removal was synthesized via a cost-effective and environment-friendly method, which could be high on the priority list owing to its high absorption capacity. By increasing the specific surface and introducing functional groups through delignification and amination, the experimental adsorption capacity of the prepared adsorbent could reach 189.9 mg/g in 180 min (pH = 4, T = 293 K, dosage = 1 g/L, and ion concentration = 300 mg/L). This value is higher than most of those achieved in previous studies on wood-based adsorbents. Pseudo-second-order and Langmuir models were utilized to describe the adsorption kinetics and isotherms, respectively. The effects of solution pH, adsorbent dosage, and temperature on the adsorption efficiency were also evaluated. With a low decrease rate of 20.2% in five cycles, the adsorbent possessed reusability. The adsorbents exhibited high selectivity in the Pb(II), Cu(II), and Zn(II) mixed solution, and the selectivity coefficient k of adsorbents to Pb(II) could reach approximately 2.74 in triad. The method could prompt the development of cost-effective methods for the removal of heavy metals from wastewater.

CAS / MDL: 10031-43-3
研究领域: 环境科学 · 材料科学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2019 · IF 6.361

Mechanistic insights into Pb(II) removal from aqueous solution by green reduced graphene oxide

Ze Lin,Xiulan Weng,Li Ma,Binoy Sarkar,Zuliang Chen

As one of the important contaminants in wastewater, Pb(II) becomes a severe public health problem because of its non-biodegradable and persistent nature. In this study, reduced graphene oxide (RGO) prepared using green tea extract was successfully used to remove Pb(II) from aqueous solutions. A 96.6% of Pb(II) was removed at 10 mg/L Pb(II) and 0.4 g/L RGO with pH 4.5 at 30 °C, and the adsorption of Pb(II) by RGO followed pseudo-second-order kinetics. To confirm the removal mechanism, various methods (Transmission Electron Microscopy, Raman spectroscopy and X-ray diffraction) were used to characterize RGO before and after Pb(II) adsorption. The results showed that the surface of RGO after Pb(II) adsorption became rougher, and the interlayer spacing increased from 0.36 nm to 0.40 nm, indicating that Pb(II) was adsorbed on the surface and between the layers of RGO. Finally, the adsorption mechanism of Pb(II) by RGO was proposed, Pb(II) was adsorbed on the surface of RGO via the electrons on the π-bond on RGO and the interaction of Pb(II) with oxygen-containing functional groups, which were supported by the Fourier Transform Infrared and X-ray photoelectron spectroscopy results.

CAS / MDL: 7782-42-5
研究领域: 环境科学 · 材料科学
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