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Journal of Cleaner Production · 2024 · IF 9.7

Synergistic effects of microplastic stability and adsorption rate on co-transport of microplastics and Pb under surfactant

Juehao Ai,Bowen Du,Xiaolong Gao,Jiachang Qiao,Shi Zhou,Xianqiang Yin,Yanji Jiang,Jun Wang,Yajie Zuo,Huimin Sun

The emergence of microplastics (MPs) and their coexistence with heavy metal contaminants pose potential risks to the safety of the subsurface environment and public health. Therefore, it is crucial to explore the co-transport of MPs (polypropylene (PP), polyethylene (PE), polystyrene (PS), polymethyl methacrylate (PMMA) and polytetrafluoroethylene (PTFE)) with the heavy metal Pb(II) under the surfactant (sodium dodecyl benzene sulfonate (SDBS) and cetyltrimethylammonium bromide (CTAB)). In this study, column experiments were performed to investigate the co-transport of MPs and Pb(II) under surfactants. The co-transport mechanism of MPs with Pb(II) under surfactant was revealed by MPs stability and batch adsorption experiments. Experimental results showed that the presence of Pb(II) did not influence the mobility of MPs under CTAB and SDBS; however, MPs can affect the mobility of Pb(II). Specifically, under CTAB, the MPs increased the recovery rate of Pb(II) from 86% to 87.55%–97.55%. However, under SDBS, the high mobility of PS, PE, and PP inhibited the transport of Pb(II), and the recoveries of Pb(II) decreased from 79% to 57.53%–70.96%. The low mobility of PTFE and PMMA slightly promoted the transport of Pb(II). This could be attributed to two reasons. One aspect is the adsorption rate of Pb(II) by MPs, which plays a pivotal role in influencing the transport tendency of Pb(II) with MPs. Another aspect is the MPs stability, as greater stability enhances their dispersity and accelerates the adsorption rate of Pb(II), thereby facilitating the co-transport of Pb(II) with MPs. This study could provide valuable insights for assessing the transport and environmental impact of MPs and heavy metals in the presence of surfactants.

CAS / MDL: 57-09-0 25155-30-0
研究领域: 环境科学 · 污染生态学
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CHEMICAL ENGINEERING SCIENCE · 2023 · IF 4.7

Synthesis, characterization of chitosan-trithiocyanuric and its removal mechanism of Cr(VI) and Pb(II) from wastewater

Wen Wang,Liqiang Qi,Song Han,Hejin Yuan

A new chitosan-trithiocyanuric composite (CS@TMT) was synthesized by graft copolymerization using chloroacetyl chloride as the cross-linking agent. Using response surface analysis, the optimal conditions for the synthesis of CS@TMT were determined as: chloroacetyl chloride concentration of 2.0 mol/L, trithiocyanuric acid (TMT) addition of 7.0 g, and reaction temperature of 70 °C. The successful preparation of CS@TMT was confirmed FTIR spectrum, 13C NMR spectrum, SEM mapping, EDS, XRD and XPS. At ambient temperature (25 °C, pH=6.0, Catalyst dosage=1.0 g/L), the maximum Cr(VI) and Pb(II) adsorption amount of CS@TMT were 194.76 and 101.39 mg/g, respectively, compared to CS (97.15 and 69.76 mg/g). The Cr(VI) and Pb(II) removal process of CS@TMT was better fitted by the pseudo-second-order kinetic model and Langmuir model, and the adsorption process was spontaneous, endothermic and disordered. Under the reduction mechanism, 69.32% of Cr(VI) was reduced to Cr(III) by -SH and –OH group on CS@TMT.

研究领域: 环境科学 · 材料科学 · 化学工程
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ACS Applied Materials & Interfaces · 2021 · IF 9.229

Synergistically Optimized Electron and Phonon Transport of Polycrystalline BiCuSeO via Pb and Yb Co-Doping

Zhanxiang Yin,Zhongyuan Liu,Yuan Yu,Cunyin Zhang,Peng Chen,Jianxun Zhao,Pan He,Xin Guo

Polycrystalline BiCuSeO is considered as a promising thermoelectric material due to its intrinsically low thermal conductivity and moderate Seebeck coefficient. However, its low electrical conductivity and coupled electron–phonon transport properties restrict the further improvement of the thermoelectric performance. In this work, Pb and Yb dopants are incorporated into BiCuSeO to substitute for Bi sites via ball milling and high-pressure and high-temperature sintering, leading to a synergistic optimization of the electron and phonon transport and improved thermoelectric performance. The carrier concentration exhibits an enhancement with increasing Pb&Yb co-doping contents. Meanwhile, the decreased carrier mobility is suppressed appropriately by coordinating with the interplay of Pb and Yb dopants on the electronic structure. Besides, Pb&Yb co-doping combined with high-pressure and high-temperature sintering introduces abundant grain boundaries, dislocations, and point defects to effectively decrease the lattice thermal conductivity by scattering phonons in a broad frequency range. Coupled with the synergistic optimization of the electrical and thermal properties, a maximum zT of 1.2 is achieved in Bi0.88Pb0.06Yb0.06CuSeO at 850 K, which significantly outperforms the majority of oxygen-containing thermoelectric materials. Our study suggests that dual doping of bivalent ions and rare-earth elements at Bi sites is an effective strategy for improving the thermoelectric performance of BiCuSeO.

研究领域: 材料科学 · 热电材料研究
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ACS Omega · 2025 · IF 4.3

Adsorption of Cu(II) and Pb(II) in Aqueous Solution by Biochar Composites

Xiaoyan Wang,Xiao Wang,Wanke Chen,Jing Yuan,Qianfeng Zhang

In this study, straw biochar (TB) was prepared by pyrolysis at 500 °C, and biochar composite material (TBS) was prepared by a 1:4 mass ratio with sludge (TS). Scanning electron microscopy and Fourier transform infrared spectroscopy were utilized to characterize the material before and after adsorption. The results demonstrated that TBS possesses significant pore structure characteristics and abundant active functional groups such as hydroxyl, carboxyl, and carbonyl groups, providing a structural basis for its efficient adsorption of heavy metal ions in aqueous solutions. The adsorption performance of the remediation materials for Cu(II) and Pb(II) in aqueous solution was systematically investigated. Experimental data showed that TBS achieved maximum adsorption capacities of 60.86 and 46.98 mg/g for Cu(II) and Pb(II) at equilibrium, respectively, exhibiting superior adsorption efficiency. Through fitting analysis using adsorption kinetic models and isothermal adsorption models, it was found that the pseudo-second-order kinetic model and Freundlich isothermal model could more accurately describe the adsorption process of the two heavy metal ions, indicating that chemical adsorption was the dominant mechanism and characterized by multilayer adsorption. Thermodynamic parameter calculations revealed negative ΔG values and positive ΔH and ΔS values, suggesting that the adsorption process was a spontaneous, entropy-increasing, and endothermic reaction. These research results fully validate the excellent removal capabilities of TBS for Cu(II) and Pb(II). This study has shown that TBS can be considered a promising and cost-effective adsorbent, demonstrating its potential to adsorb heavy metal ions in water.

CAS / MDL: 7447-39-4 7758-95-4
研究领域: 环境科学 · 材料科学
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WATER AIR AND SOIL POLLUTION · 2024 ·Vol. 235 ·期 10 ·1-15 · IF 3.8

Gangue-Based SiO2 Aerogel Used for Pb(II) Adsorption in Wastewater and Mechanism Analysis

Liu Xu,Kong Xiaomin,Wen Hao,Wang Yue,Wu Meili,Yin Hongwei,Qin Wei,Wang Manli,Pei Jun,Qu Miaoming

Coal gangue, a byproduct of coal mining with massive generation, presents a major challenge for resource utilization. In this study, SiO 2 aerogel was successfully fabricated from coal gangue, via a facile and cost-effective approach. The aerogel boasts an intricate network framework structure internally and functions as a mesoporous material with measurements of 154.5662 m 2 ·g −1 for specific surface area and 7.9557 nm for average pore size. Additionally, exploring the adsorption capabilities of SiO 2 aerogel concerning Pb(II) in wastewater, the research revealed insights. The results demonstrated that the maximum Pb(II) removal efficiency reached 94.09% under pH 6, aerogel dosage of 1.5 g·L⁻ 1 , and initial Pb(II) concentration of 80 mg·L⁻ 1 . The adsorption process followed the Langmuir isotherm model and pseudo-second-order kinetic model, suggesting a favorable and predominantly monomolecular layer chemisorption, and the intraparticle diffusion model suggests internal diffusion behavior during adsorption. The SiO 2 aerogel exhibited specific adsorption behavior towards Pb(II). This study offers a promising avenue for repurposing coal gangue while addressing the issue of Pb(II)-contaminated wastewater.

研究领域: 环境科学 · 材料科学
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CERAMICS INTERNATIONAL · 2020 · IF 3.83

Structural origin of size effect on piezoelectric performance of Pb(Zr,Ti)O3

Shengdong Sun,Hui Liu,Longlong Fan,Yang Ren,Xianran Xing,Jun Chen

Grain size effect plays a vital role in piezoelectric performance from both scientific and technological view. However, the underlying structural mechanism related to grain size is still unclear. In the present study, the structural mechanism of grain size effect on piezoelectric performance has been revealed in the prototype Pb(Zr,Ti)O 3 system by using in-situ synchrotron X-ray diffraction. The miniaturization of grain size tends to favor the appearance of higher symmetric tetragonal phase, while a single monoclinic phase is determined in the coarse-grained ceramics. The direct structural evidence reveals that both tetragonal and monoclinic phases in the fine-grained ceramics are less sensitive to the electric field, corresponding to the inferior piezoelectric performance, while the single monoclinic phase in the coarse-grained ceramics is more active to be driven by the electric field, generating good piezoelectric behavior. Both domain switching ability and lattice strain are suppressed with decreasing grain size, which directly leads to the deterioration in piezoelectric performance. The current results will benefit the structural understanding of the size effect of piezoelectric and other related systems.

研究领域: 材料科学 · 物理学
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LANGMUIR · 2025 · IF 3.9

Design and Characterization of Concave Hollow Double-Layer Nanospheres for Efficient Cd(II) and Pb(II) Adsorption

Fangfen Jing,Xin Xu,Weiwei Lu,Mingzhu Jin,Xinyang He,Rongtai Yu

Polymer-based adsorbents have emerged as promising candidates for heavy-metal remediation due to their tailorable porosity and multifunctional surfaces, yet challenges persist in achieving both structural precision and adsorption efficiency. Here, we report a concave hollow double-layer nanosphere (CHDN) synthesized through a facile self-assembly strategy engineered for selective capture of Cd(II) and Pb(II) ions. Comprehensive characterization via transmission electron microscopy (TEM), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, and thermogravimetric analysis (TGA) confirmed the hierarchical architecture with abundant amino/hydroxyl moieties. The CHDN demonstrated exceptional adsorption capacities of 198.40 mg/g for Cd(II) and 60.34 mg/g for Pb(II), outperforming conventional adsorbents. Isotherm analysis revealed Cd(II) adsorption followed the Sips model (R2 > 0.99), while Pb(II) adhered to the Langmuir model, suggesting monolayer and heterogeneous binding mechanisms, respectively. Kinetic studies further corroborated chemisorption dominance through pseudo-second-order fitting for Cd(II) and Elovich compatibility for Pb(II). We propose a synergistic mechanism involving ligand complexation and ion exchange, facilitated by the dual functionality of surface groups and structural advantages of the concave architecture. This work provides a blueprint for designing spatially engineered polymers for environmental remediation.

研究领域: 环境科学 · 材料科学
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Royal Society Open Science · 2020 ·Vol. 7 ·期 3 · IF 2.646

Corn stalk as starting material to prepare a novel adsorbent via SET-LRP and its adsorption performance for Pb(II) and Cu(II)

Yazhen Wang,Shuang Li,Liqun Ma,Shaobo Dong,Li Liu

Corn stalk was used as the initial material to prepare a corn stalk matrix-g-polyacrylonitrile-based adsorbent. At first, the corn stalk was treated with potassium hydroxide and nitric acid to obtain the corn stalk-based cellulose (CS), and then the CS was modified by 2-bromoisobutyrylbromide (2-BiBBr) to prepare a macroinitiator. After that, polyacrylonitrile (PAN) was grafted onto the macroinitiator by single-electron transfer living radical polymerization (SET-LRP). A novel adsorbent AO CS-g-PAN was, therefore, obtained by introducing amidoxime groups onto the CS-g-PAN with hydroxylamine hydrochloride (NH2OH · HCl). FTIR, SEM and XPS were applied to characterize the structure of AO CS-g-PAN. The adsorbent was then employed to remove Pb(II) and Cu(II), and it exhibited a predominant adsorption performance on Pb(II) and Cu(II). The effect of parameters, such as temperature, adsorption time, pH and the initial concentration of metal ions on adsorption capacity, were examined in detail during its application. Results suggest that the maximum adsorption capacity of Pb(II) and Cu(II) was 231.84 mg g–1 and 94.72 mg g−1, and the corresponding removal efficiency was 72.03% and 63%, respectively. The pseudo-second order model was more suitable to depict the adsorption process. And the adsorption isotherm of Cu(II) accorded with the Langmuir model, while the Pb(II) conformed better to the Freundlich isotherm model.

研究领域: 环境科学 · 材料科学
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Nature Communications · 2024 ·Vol. 15 ·期 1 ·1-9 · IF 14.7

Pinning effect of lattice Pb suppressing lattice oxygen reactivity of Pb-RuO2 enables stable industrial-level electrolysis

Zhou Chenhui,Li Lu,Dong Zhaoqi,Lv Fan,Guo Hongyu,Wang Kai,Li Menggang,Qian Zhengyi,Ye Na,Lin Zheng,Luo Mingchuan,Guo Shaojun

Ruthenium (Ru) is widely recognized as a low-cost alternative to iridium as anode electrocatalyst in proton-exchange membrane water electrolyzers (PEMWE). However, the reported Ru-based catalysts usually only operate within tens of hours in PEMWE because of their intrinsically high reactivity of lattice oxygen that leads to irrepressible Ru leaching and structural collapse. Herein, we report a design concept by employing large-sized and acid-resistant lattice lead (Pb) as a second element to induce a pinning effect for effectively narrowing the moving channels of oxygen atoms, thereby lowering the reactivity of lattice oxygen in Ru oxides. The Pb-RuO 2 catalyst presents a low overpotential of 188 ± 2 mV at 10 mA cm −2 and can sustain for over 1100 h in an acid medium with a negligible degradation rate of 19 μV h −1 . Particularly, the Pb-RuO 2 -based PEMWE can operate for more than 250 h at 500 mA cm −2 with a low degradation rate of only 17 μV h −1 . Experimental and theoretical calculation results reveal that Ru-O covalency is reduced due to the unique 6 s −2 p −4 d orbital hybridization, which increases the loss energy of lattice oxygen and suppresses the over-oxidation of Ru for improved long-term stability in PEMWE.

CAS / MDL: 10099-74-8
研究领域: 电化学 · 材料科学 · 催化 · 能源存储与转换
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Small · 2021 ·Vol. 17 ·期 8 ·2006111 · IF 13.281

Pb-Doped Ag2Se Quantum Dots with Enhanced Photoluminescence in the NIR-II Window

Mengxuan Yu,Xiaohu Yang,Yejun Zhang,Hongchao Yang,Haoying Huang,Zan Wang,Jinyi Dong,Rong Zhang,Ziqiang Sun,Chunyan Li,Qiangbin Wang

Ag 2 Se quantum dots (QDs) as an effective biological probe in the second near-infrared window (NIR-II, 1000–1700 nm) have been widely applied in bioimaging with high tissue penetration depth and high spatiotemporal resolution. However, the ions deficiency and crystal defects caused by the high Ag + mobility in Ag 2 Se crystals are mainly responsible for the inefficient photoluminescence (PL) of Ag 2 Se QDs. Herein, a tailored route is reported to achieve controllable doping of Ag 2 Se QDs in which Ag is exchanged by Pb via cation exchange (CE), which is unattainable by direct synthetic methods. The Pb-doped Ag 2 Se QDs (denoted as Pb:Ag 2 Se QDs) present fire-new optical features with significantly enhanced PL intensity of 4.2 folds. Photoelectron spectroscopy confirms that Pb acts as an n-type dopant for Ag 2 Se QDs and therefore the electronic impurities provide additional carriers to fill the traps. Moreover, the general validity of this method is demonstrated to convert different sized Ag 2 Se into Pb:Ag 2 Se QDs, so that a wide range of NIR-II PL with high intensity is obtained. The bright NIR-II emission of Pb:Ag 2 Se QDs is further successfully performed in lymphatic system mapping.

研究领域: 生物医学工程 · 材料科学 · 光学成像
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CERAMICS INTERNATIONAL · 2025 · IF 5.6

The enhanced thermoelectric properties of Pb-doped Cu2.85Ag0.15Sb0.985−xBi0.015Se4 samples synthesized via vacuum melting and cold isostatic pressing

Honglei Wang,Zixuan Tian,Zhuang Fu,Lijun Zhao,Lei Wang,Songtao Dong,Hongbo Ju

Cu 3 SbSe 4 has garnered significant attention due to its low thermal conductivity, complex elemental composition, and economic feasibility. In this study, Cu 2.85 Ag 0.15 Sb 0.985−x Bi 0.015 Pb x Se 4 (x=0, 0.05, 0.10, and 0.15) samples were synthesized using a system of vacuum melting combined with cold isostatic pressing techniques. The impact of Pb doping on the thermoelectric properties of Cu 2.85 Ag 0.15 Sb 0.985 Bi 0.015 Se 4 was comprehensively investigated. The experimental results revealed a notable increase in carrier concentration, from 2.95×10 18 cm −3 to 8.31×10 19 cm −3 , leading to a substantial improvement on the electrical conductivity. At 573 K, the electrical conductivity of the Cu 2.85 Ag 0.15 Sb 0.835 Bi 0.015 Pb 0.15 Se 4 reached 234.26 S cm −1 , while the power factor of the Cu 2.85 Ag 0.15 Sb 0.885 Bi 0.015 Pb 0.10 Se 4 achieved a maximum value of 883.5 μW m −1 K −2 . The incorporation of Pb induced lattice defects, which modified the phonon mean free path and enhanced phonon scattering. As a result, the increased phonon scattering contributed to a reduction in lattice thermal conductivity within the Cu 2.85 Ag 0.15 Sb 0.985 Bi 0.015 Se 4 sample. The thermoelectric figure of merit (ZT) for the Cu 2.85 Ag 0.15 Sb 0.935 Bi 0.015 Pb 0.05 Se 4 reached a peak value of approximately 0.74 at 573 K, marking a 157.4% improvement compared to that of Cu 2.85 Ag 0.15 Sb 0.985 Bi 0.015 Se 4 (∼0.47). This study demonstrates that multi-element doping is a highly effective strategy for optimizing the thermoelectric properties of the Cu 3 SbSe 4 system.

CAS / MDL: 7439-92-1 7440-22-4
研究领域: 材料科学 · 热电材料研究
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Advanced Optical Materials · 2025 · IF 7.2

Sustainable Rejuvenation of Scalable Large-Area WO3-PB Electrochromic Devices

Haopeng Jing,Chunjian Wang,Kun Li,Ran Jiang,Jumei Zhou,Hongtao Cao,Hongliang Zhang

Electrochromic devices (ECD) have become a hot research topic in the field of green buildings due to their excellent energy efficiency and thermal management capabilities. Currently, challenges such as difficulties in large-area preparation, high costs, and degradation of electrochromic performance over time have hindered their widespread application. A strategy incorporating a dual-phase nanocrystalline structure of WO 3 and TiO 2 ·H 2 O is proposed, in which specific synthesis parameters are precisely controlled to tailor the microstructure and composition of the films, enabling the fabrication of large-area WO 3 -PB ECD with UV-rejuvenation electrochromic performance. As a result, the as-prepared WO 3 -PB ECD exhibits an optical modulation of 75.6% and a remarkable cycle life exceeding 13,000 cycles. The electrochromic performance degradation caused by long cycles can be restored via UV irradiation. Utilizing UV light to restore the performance of these WO 3 -PB ECDs promotes sustainable and environmentally friendly development, highlighting their important practical value.

CAS / MDL: 7440-33-7
研究领域: 绿色建筑技术 · 材料科学 · 纳米技术 · 能源效率 · 光电子学
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