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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2021 · IF 4.539

Experimental and theoretical study on the adsorption mechanism of Amino trimethylphosphate (ATMP) functionalized hydroxyapatite on Pb (II) and Cd (II)

Yanru Zhang,Mingzhu Xia,Fengyun Wang,Jianzhe Ma

Amino trimethylposphonate(ATMP) functionalized HAP were synthesized with different ATMP addition (0, 5%, 10%, 15%) and the adsorption performance towards Pb 2+ and Cd 2+ were studied in an aqueous solution. Under the optimum condition, HAP with ATMP addition of 10% (10AT-HAP) displayed the most efficient adsorption performance with the adsorption capacity of 1458.79 mg/g and 321.26 mg/g towards Pb 2+ and Cd 2+ , respectively, which improved 76% and 92% than that of the artificially prepared HAP in the laboratory, respectively. For both heavy metal ions , the adsorption mechanism also included ion exchange and surface complexation, in which the surface complexation played a predominant role. In addition, XRD showed that a new crystal phase was formed after Pb 2+ adsorption, while no new phase appeared after Cd 2+ adsorption, indicating that the adsorption mechanism of Pb 2+ involved dissolution-precipitation. The fitting results of adsorption isotherm and kinetics showed that the adsorption of Pb 2+ and Cd 2+ on HAP and 10AT-HAP were well fitted by the Langmuir isotherm model and Pseudo-second model. Moreover, Multiwfn wavefunction program based on density functional theory (DFT) was applied to deeply probe and vividly visualize the interaction sites, interaction types, interaction strength and the essence of interactions between HAP and ATMP or ATMP-HAP composite and heavy metal ions.

研究领域: 环境科学 · 材料科学
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Journal of Environmental Chemical Engineering · 2023 · IF 7.7

Three-dimensional porous AuNPs-decorated polyaniline array for ultrasensitive determination of trace Cd(II) and Pb(II) in drinking water

Guodong Zhu,Chengwei Feng,Lin Wang,Chenkai Zhou,Xiaole Weng,Kun Yang

Herein, a three-dimensional porous nanomaterials AuNPs-decorated polyaniline nanowire arrays/carbon nanotube (Au-PANI-array@CNT) was constructed by modified dilute polymerization and redox reaction. The Au-PANI-array@CNT exhibited a larger specific surface area (50.03 m 2 g −1 ) and abundant mesopores (average pore size: 19.6 nm), due to the vertical growth of PANI nanowire arrays on CNT. The Au-PANI-array@CNT composite with a three-dimensional interconnected porous structure exhibited abundant electroactive sites and high adsorption capacity, significantly enhancing the deposition and electrochemical reaction process of heavy metals. The AuNPs embedded on PANI nanowries can provide high catalytic activity and multidimensional electron transport channels, further improving the detection sensitivity. A sensing platform with ultra-high sensitivity (2091, 3890 μA μM −1 cm −2 ) and lower limit of detection (0.18, 0.15 nM) for Cd(II) and Pb(II) determination was developed based on the three-dimensional porous PANI composite. Furthermore, the sensing mechanism of Au-PANI-array@CNT with Cd(II) was explored by XPS and FTIR spectroscopy . The current response only decreased by 5% after being stored at room temperature for 2 months, indicating that the sensor has high reproducibility and stability. Finally, the analysis of drinking water samples verified the excellent practicability of the sensor for the simultaneous measurement of trace levels (nM) of Cd(II) and Pb(II).

CAS / MDL: 7727-54-0 16903-35-8
研究领域: 环境科学 · 材料科学 · 分析化学
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Journal of Environmental Chemical Engineering · 2023 · IF 7.7

Recognizing adsorption of aqueous Cr(VI), As(III), Cd(II), and Pb(II) ions by amino groups hollow polymer adsorbent

Yueyang Wang,Mingzhu Jin,Weiwei Lu,Fangfen Jing,Xinyang He,Jianchao Xie,Rongtai Yu

The mechanism from the molecular level and the selectivity for the removal of metal ions from aqueous has become a hotspot in current water treatment . In this study, a sulphydryl-modified hollow polymer adsorbent was designed with intrinsic amine and grafted sulphydryl groups for efficient uptake of Cr(VI), As(III), Cd(II), and Pb(II) by taking advantage of their properties of abundant functional groups, discrete hollow chambers, and high porosity. Interestingly, the benzenoid amine/quinoid imine functional groups have a stronger affinity for Cr(VI) than Cd(II) or As(III) and Pb(II). The formation of approximately 65.7% Cr(III) indicates the redox reaction from Cr(VI) to Cr(III). The electron-donating comes from benzenoid amine and oxidized to quinoid imine or protonated oxidized nitrogen units (-N =  + ) with Cr(VI) reduced to Cr(III) for the increase of more than double of quinoid imine and a new functional group of -N =  + . Ion exchange between –COO - groups and As(III)/Cd(II), the chelation of –SH groups for Pb(II)/As(III) are plausible mechanisms.

研究领域: 环境科学 · 水处理技术
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LANGMUIR · 2023 · IF 3.9

Sulfhydryl-Functionalized Amino Group Polymer Microcomposites toward Efficient Adsorption of Aqueous Cr(VI), As(III), Cd(II), and Pb(II)

Yueyang Wang,Weiwei Lu,Fangfen Jing,Mingzhu Jin,Xinyang He,Yuchen Xue,Yajun Hu,Rongtai Yu

The development of efficient adsorbents for heavy metal pollution, especially five toxic heavy metals, has attracted great research interest. Polymer-based adsorbents have aroused research value for their abundant functional groups and high porosity to the ability to capture metal ions. We designed a sulfhydryl-functionalized polymer microcomposite to take up Cr(VI), As(III), Cd(II), and Pb(II). The adsorption capacity achieved was 64.2 mg g–1 for Cr(VI), 44.9 mg g–1 for As(III), 35.5 mg g–1 for Cd(II), and 18.2 mg g–1 for Pb(II). Langmuir and Sips isotherm model is dominant for As(III), Cd(II), and Pb(II) adsorption. Pseudo-second-order kinetic models can better describe the adsorption behavior of Cr(VI), implying that chemisorption is accompanied by Cr(VI) adsorption. Cr(VI) simultaneous reduction to Cr(III) through the benzenoid amine oxidate pathway was the dominant mechanism, precipitation for Cd(II) adsorption was convinced, and chelation between As(III)/Pb(II) and─SH group and complexation between Pb(II) and C═O or benzene hydroxyl were a plausible mechanism for As(III) and Pb(II) adsorption.

研究领域: 环境科学 · 材料科学
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FOOD CHEMISTRY · 2023 · IF 8.8

Bipotential-resolved electrochemiluminescence biosensor based on Bi2S3@Au nanoflowers for simultaneous detection of Cd(II) and ampicillin in aquatic products

Hongguo Zhai,Yue Wang,Lingjun Geng,Qi Guo,Yuhao Zhang,Qingqing Yang,Xia Sun,Yemin Guo,Yanyan Zhang

In this paper, an electrochemiluminescence (ECL) biosensor was constructed using Bi 2 S 3 @Au nanoflowers as the based nanomaterial and [email protected] and CdS QDs as independent ECL emission signal respectively. As the substrate of the working electrode, Bi 2 S 3 @Au nanoflowers improved the effective area of electrode and accelerated electron transfer rate between gold nanoparticles and aptamer, provided a good interface environment for the loading of luminescent materials. Then, the [email protected] functionalized DNA2 probe was used as an independent ECL signal source under positive potential and recognized Cd(II), while the CdS QDs functionalized DNA3 probe was used as an independent ECL signal source under negative potential and recognized ampicillin. The simultaneous detection of Cd(II) and ampicillin in different concentrations are realized. This sensor not only has good selectivity and high sensitivity in real sample detection, but also open up a novel way to construct multi-target ECL biosensor for simultaneous detection.

CAS / MDL: 25952-53-8 106627-54-7
研究领域: 分析化学 · 环境科学 · 食品安全 · 纳米材料 · 生物化学
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JOURNAL OF HAZARDOUS MATERIALS · 2023 · IF 13.6

Responses of a polycyclic aromatic hydrocarbon-degrading bacterium, Paraburkholderia fungorum JT-M8, to Cd (II) under P-limited oligotrophic conditions

Jinghua Li,Yiwen Ou,Lijuan Wang,Yue Zheng,Weiyun Xu,Jianbiao Peng,Xin Zhang,Zhiguo Cao,Junpei Ye

For the bioremediation of mixed-contamination sites, studies on polycyclic aromatic hydrocarbon (PAH) degradation or Cd (II) tolerance in bacteria are commonly implemented in nutrient-rich media. In contrast, in the field, inocula usually encounter harsh oligotrophic habitats. In this study, the environmental strain Paraburkholderia fungorum JT-M8 was used to explore the overlooked Cd (II) defense mechanism during PAH dissipation under P-limited oligotrophic condition. The results showed that the growth and PAH degradation ability of JT-M8 under Cd (II) stress were correlated with phosphate contents and exhibited self-regulating properties. Phosphates mainly affected the Cd (II) content in solution, while the cellular distribution of Cd (II) depended on Cd (II) levels; Cd (II) was mainly located in the cytoplasm when exposed to less Cd (II), and vice versa. The unique Cd (II) detoxification pathways could be classified into three aspects: (i) Cd (II) ionic equilibrium and dose–response effects regulated by environmental matrices (phosphate contents); (ii) bacterial physiological self-regulation, e.g., cell surface-binding, protein secretion and active transport systems; and (iii) specific adaptive responses (flagellum aggregation). This study emphasizes the importance of considering culture conditions when assessing the metal tolerance and provides new insight into the bacterial detoxification process of complex PAH-Cd (II) pollutants.

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CHEMOSPHERE · 2024 · IF 8.1

Aging properties of polyethylene and polylactic acid microplastics and their adsorption behavior of Cd(II) and Cr(VI) in aquatic environments

Xinying Zhang,Yuling Zhang,Dong Li,Jili Wang,Yang Ding,Yiliang Wang,Liuyuan Feng,Yuliang Hu

In this study, we examined the aging characteristics of polyethylene (PE) and polylactic acid (PLA) microplastics (MPs), examining the adsorption behaviors and mechanisms concerning Cd(II) and Cr(VI) under both single and binary systems. The results revealed that aging treatment changed the physicochemical properties of MPs. The aging mechanisms of PLA and PE MPs were shown to be similar by the 2D-FTIR-COS study. These mechanisms involve the formation of oxygen-containing functional groups through the combination of carbon chain breakdown and oxygen. Aged MPs had a greater ability to adsorb metal ions than pristine MPs, with PLA MPs outperforming PE MPs. After 30 days of aging, Cd(II) adsorption increased by 40.61 % and 25.49 % for PE and PLA MPs, respectively, while Cr(VI) adsorption increased by 37.50 % and 69.29 %, respectively. The adsorption ability of PE and PLA MPs with Cd(II) or Cr(VI) under binary systems was less than that under single systems, with Cd(II) exhibiting more adsorption competitiveness than Cr(VI). Humic acid (HA), ionic species and strength , solution pH, and adsorption of Cd(II) and Cr(VI) were found to be significantly correlated. Further investigation into the adsorption mechanisms of Cd(II) and Cr(VI) on PE and PLA MPs revealed that pore-filling, electrostatic interactions , complexation, and hydrogen bonding play important roles in the adsorption process . The study's conclusions are crucial for assessing the risk associated with concurrent contamination by metal ions and microplastics.

CAS / MDL: 1415-93-6
研究领域: 环境科学 · 材料科学 · 化学
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MOLECULES · 2024 ·Vol. 29 ·期 11 ·2665 · IF 4.2

Conversion of Phosphogypsum into Porous Calcium Silicate Hydrate for the Removal and Recycling of Pb(II) and Cd(II) from Wastewater

Gangan Wang,Chaoyi Chen,Junqi Li,Yuanpei Lan,Xin Lin,Jiahang Chen

The discharge of lead and cadmium wastewater, along with the pollution caused by phosphogypsum, represents a particularly urgent environmental issue. This study employed a straightforward hydrothermal method to convert phosphogypsum into porous calcium silicate hydrate (P-CSH), which was then used to remove and recover Pb(II) and Cd(II) from wastewater. The adsorption capacities of P-CSH for Pb(II) and Cd(II) were notably high at 989.3 mg/g and 290.3 mg/g, respectively. The adsorption processes adhered to the pseudo-second-order kinetics model and the Langmuir isotherm model. Due to identical adsorption sites on P-CSH for both Pb(II) and Cd(II), competitive interaction occurred when both ions were present simultaneously. Additionally, the adsorption efficacy was minimally impacted by the presence of common coexisting cations in wastewater. The dominant mechanisms for removing Pb(II) and Cd(II) via P-CSH were chemical precipitation and surface complexation. Moreover, the adsorbed heavy metals were efficiently separated and reclaimed from the wastewater through a stepwise desorption process. The primary components of the residue from stepwise desorption were quartz and amorphous SiO2. Following dissolution via pressurized alkaline leaching, this residue could be recycled for synthesizing P-CSH. This research offered a new strategy for the resourceful use of phosphogypsum and heavy metal wastewater.

CAS / MDL: 13517-24-3 7631-99-4
研究领域: 环境科学 · 材料科学 · 化学工程
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY · 2017 ·Vol. 164 ·期 13 ·H967 · IF 3.259

Sensitive and Selective Differential Pulse Voltammetry Detection of Cd(II) and Pb(II) Using Nitrogen-Doped Porous Carbon Nanofiber Film Electrode

Sanshuang Gao,Chuyang Xu,Nuerbiya Yalikun,Xamxikamar Mamat,Yongtao Li,Thomas Wågberg,Xun Hu,Jing Liu,Jun Luo,Guangzhi Hu

Carbon matrix materials are regarded as one of the most important electrode materials for heavy metal detection. But even so, optimization procedures of carbon nanofibers (CNFs) for tracing Cd(II) and Pb(II) remains challenging. Here, zeolitic imidazolate framework (ZIF-8)/polyacrylonitrile (PAN)-derived nitrogen-doped porous carbon nanofibers (N-PCNFs) were investigated as a new electrode material for determining the concentration of Cd(II) and Pb(II). By optimizing electrochemical conditions such as deposition potential, deposition time, pH of buffer solution, and quantity of N-PCNFs loaded on a glassy carbon electrode (GCE), the linear response curves of Cd(II) and Pb(II) could be obtained. Due to the unique structural feature and N content, the N-PCNFs possess excellent detection limits of 0.8 μg L−1 for Cd(II) and 0.3 μg L−1 for Pb(II) (S/N = 3). To manifest the practical use of the sensor platform the concentration of Cd(II) and Pb(II) in normal tap and waste water were monitored. According to the ICP-MS results, the calculated recovery (97.0–107%) indicates that N-PCNFs have potential as a candidate material to monitor the concentration of Cd(II) and Pb(II) in practical samples.

研究领域: 环境科学 · 材料科学 · 分析化学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2022 · IF 5.518

A polyrutin/AgNPs coated GCE for simultaneous anodic stripping voltammetric determination of Pb(II) and Cd(II)ions in environmental samples

Zhou Liuzhu,Sankar Sekar,Jin Chen,Sejoon Lee,Deuk Young Kim,Ramalingam Manikandan

Here, we report a simple one-step preparation of polyrutin/silver nanoparticles (AgNPs) on the glassy carbon electrode (GCE) surface using an electrochemical deposition/polymerization technique. As prepared polyrutin/AgNPs/GCE has been characterized by different techniques such as SEM with elemental morphing, TEM with EDAX , XRD , ATR-IR to confirm the materials formation. Further, electrochemical behavior of the polyrutin/AgNPs/GCE was tested by cyclic voltammetry , EIS and differential pulse voltammetric techniques. As fabricated polyrutin/AgNPs/GCE was used for simultaneous detection of Pb(II) and Cd(II)ions using anodic stripping voltammetric techniques and stripping analysis of Pb(II) and Cd(II)ions analytical parameters like pH, preconcentration time were studied. The polyrutin/AgNPs/GCE has showed a linear concentration range from 29 nM to 140 nM and 57–203 nM with detection limit of 3 nM and 10 nM for Pb(II) Cd(II)ions respectively. Further, the modified electrode was tested towards detection of these heavy metal ions in different environmental samples and the found excellent recovery results were further correlated with ICP-MS results.

研究领域: 环境科学 · 分析化学
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Journal of Materials Chemistry A · 2018 ·Vol. 6 ·期 41 ·20110-20120 · IF 9.931

Pb(II), Cu(II) and Cd(II) removal using a humic substance-based double network hydrogel in individual and multicomponent systems

Jianhong Ma,Jinming Luo,Yutang Liu,Yuanfeng Wei,Tao Cai,Xingwen Yu,Hui Liu,Chengbin Liu,John C. Crittenden

A systematic study of the interaction between adsorbents and potentially toxic metal ions in multicomponent systems is of great significance due to the coexistence of multiple potentially toxic metal ions in the real water environment. In this study, a new humic substance-based double network hydrogel (PAA/HS gel) was produced by a radical polymerization method and applied to Pb(II), Cu(II) and Cd(II) removal in both individual and multicomponent systems under various conditions. The macroporous network structure (aperture ≈ 10 μm) and high water permeability of the PAA/HS gel could fully facilitate the active site exposure and increase the potentially toxic metal ion diffusion rate. The PAA/HS gel exhibited high theoretical adsorption capacities of 360.50, 151.00 and 412.76 mg g−1 for Pb(II), Cu(II) and Cd(II) in individual systems. Noticeably, both interference and promotion of adsorption behaviors were identified in multicomponent systems. In binary systems, the adsorption capacity and rate were decreased for Pb(II) and Cu(II), while increased for Cd(II). In ternary systems, the adsorption capacity and rate for Pb(II), Cu(II) and Cd(II) were decreased. The adsorption isotherms and kinetics were well fitted by Langmuir–Freundlich and Elovich models, respectively, indicating that the PAA/HS gel possessed a heterogeneous surface and various types of binding sites. The FTIR and XPS studies confirmed that both nitrogen- and oxygen-containing functional groups (i.e., amino, phenolic hydroxyl and carboxyl groups) were involved in the adsorption process, while the interactions between functional groups and Pb(II), Cu(II) and Cd(II) were different.

研究领域: 环境科学 · 材料科学
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CHEMICAL ENGINEERING JOURNAL · 2026 · IF 12.5

Dual-functionalized Fe(BTC)₈(PABA)₂ for ultrafast and ultrahigh-capacity capture of Cd(II) and Pb(II) with multiscale mechanistic insights

Kai Wang,Chunqing Niu,Xin Zhang,Nuo Liu,Zhengxin Luo,Chunhong Zhu,Jian Shi

A mixed mono−/multidentate ligand strategy engineered defective MIL-100(Fe). • Coordinatively unsaturated Fe O sites promoted rapid heavy-metal adsorption. • Defect engineering integrated Fe O exposure and amino functionalization. • Synergistic Fe–O/NH₂/COO − sites enhanced adsorption kinetics and affinity. • A flexible MOF membrane achieved efficient and recyclable heavy-metal removal. To address Pb(II) and Cd(II)-dominated heavy-metal contamination in water, a series of amino-bearing, defect-regulated Fe-based metal-organic frameworks (MOFs) were constructed using ligand engineering. In the synthetic design, the tritopic linker 1,3,5-benzenetricarboxylic acid (H₃BTC) was coupled with the monotopic modulator p-aminobenzoic acid (PABA), enabling the simultaneous generation of coordinatively unsaturated Fe O centers and exposed -NH₂ functionalities within the framework. This dual functionalization substantially strengthened the affinity of the adsorbent for divalent heavy-metal ions. Among the obtained samples, 6 mg Fe(BTC)₈(PABA)₂, corresponding to an H₃BTC/PABA feed ratio of 8:2, delivered the best adsorption performance under the conditions of 25 °C, pH 5, and an initial concentration of 150 mg/L, with maximum uptake values of 732.03 mg/g for Pb(II) and 654.05 mg/g for Cd(II), and equilibrium was achieved within 15 min. Kinetic and equilibrium analyses followed the pseudo-second-order model and Langmuir isotherm, respectively, indicating that monolayer chemisorption dominates the capture process. To improve the handling, recovery, and reusability of Fe(BTC)₈(PABA)₂ particles, they were incorporated into a polyacrylonitrile (PAN) nanofibrous matrix via electrospinning to obtain a Fe(BTC)₈(PABA)₂@PAN membrane. The membrane retained good structural stability and pronounced selectivity, particularly for Pb(II), in both binary-ion media and multi-cationic aqueous systems. After five adsorption-desorption cycles, more than 83% of the initial adsorption capacity was retained. DFT (Density functional theory) calculations further supported the experimental observations, showing that the adsorption originated from cooperative coordination among unsaturated Fe-O-M sites, carboxyl oxygen atoms, and amino nitrogen atoms. Therefore this study provides a defect- and functionality-coupled strategy for developing MOF-based adsorbents with both rapid uptake and high capacity for heavy-metal remediation. Download: Download high-res image (331KB) Download: Download full-size image

CAS / MDL: 25014-41-9
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