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DESALINATION · 2026 · IF 9.9

LLTO-Al2O3 composite ceramic membrane for selective lithium extraction from high Mg2+/Li+ ratio brine via electrodialysis: Fabrication, ion transport, and performance

Jilong Han,Ruyi Shi,Mochi Li,Huanzhang Lu,Yijian Zheng,Pengfei Li,Jisheng Li

Dense LLTO-Al 2 O 3 membrane (∼20 μm) for /Li + from high Mg 2+ /Li + brine. • Optimised LLTO (x = 0.11, 1250 °C/6 h): tetragonal, 3.26 × 10 3  S/cm. • La-poor/La-rich enables 2D Li + transport; Mg 2+ blocked by size. • Intergranular defects are main pathway for Mg 2+ co-permeation. • Selectivity 16.06, 99.61% Mg 2+ rejection (6 h); energy 23.21 kW·h (24 h). To solve the problem of lithium extraction from salt lake brine with a high magnesium‑lithium ratio, a composite ceramic membrane electrodialysis technology based on perovskite-type superionic conductor Li 3x La 2/3-x TiO 3 (LLTO) was proposed. LLTO powder was synthesised by the sol-gel method. The lithium doping amount (x = 0.11), sintering temperature (1250 °C) and time (6 h) were systematically optimised to obtain tetragonal LLTO with high ionic conductivity (3.26 × 10 −3  S/cm). Then, the LLTO-Al 2 O 3 composite film was prepared by a spin coating process (PVA content of 20%, LLTO solid content of 0.08 g/mL, spin coating 10 times) with porous alumina as the substrate. After calcination at 1275 °C for 6 h, a dense film with a thickness of about 20 μm was formed. Molecular dynamics simulations show that the two-dimensional selective transport of Li can be realised in the LLTO inner layer based on the La-poor / La-rich alternating structure, while Mg 2+ is hindered by the size effect. Intergranular defects are the main pathway leading to the co-permeation of Mg 2+ . The electrodialysis experiment showed that the membrane had good selectivity (selectivity coefficient 16.06) and Mg 2+ rejection rate (99.61%) for Li at the initial stage of operation (6 h), and the energy consumption was 23.21 kWh after 24 h of electrodialysis. This study provides a reference for membrane material design, preparation process and transmission mechanism for lithium extraction from high magnesium‑lithium ratio brine, and has potential application value.

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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

Machine learning-driven QSAR study on efficient extractants for Mn2+-Mg2+ separation: Impact of steric hindrance and electronic characteristics on extraction performance

Xintong Li,Xiaoya Li,Xin Ma,Zhanfang Cao,Hong Zhong,Shuai Wang

Manganese is a critical metal with widespread applications. The increasing demand for manganese, driven by the rapid growth of the electric vehicle and new energy sectors, has underscored the need for efficient separation and purification technologies, particularly from low-grade ores with high content of impurities. This study applies machine learning (ML) −driven quantitative structure–activity relationship (QSAR) modeling to investigate the Mn 2+ and Mg 2+ separation performance of 14 extractants. Key molecular descriptors were identified through principal component analysis and clustering heatmap method, and QSAR models were developed using ordinary least squares, nonlinear model, artificial neural network, random forest, and extreme gradient boosting (XGBoost) tree. The XGBoost model exhibited superior predictive accuracy for Mn 2+ and Mg 2+ extraction efficiencies and Mn 2+ /Mg 2+ separation selectivity. Feature importance analysis revealed that molecular properties related to hydrophilicity, electronic characteristics, and steric hindrance, as reflected by descriptors such as Clog P, OAV, Nonpolar S, VIP, Max P, and EI, play decisive roles in governing extraction efficiency and separation performance. Further NCI analysis demonstrated that the C–OH group of one α -hydroxyalkyl phosphinic acid ( α -HA) molecule forms a hydrogen bond with the C–OH group of another α -HA molecule, which likely accounts for the tendency of α -HA molecules to form dimers during solvent extraction. This interaction modulates the spatial arrangement of P–OH and P=O groups, enhancing both Mn 2+ extraction efficiency and Mn 2+ /Mg 2+ separation selectivity. These findings underscore the value of ML-driven QSAR modeling in predicting extractant performance, offering new mechanistic insights into Mn 2+ /Mg 2+ separation, and informing the development of novel extractants.

研究领域: 化学工程 · 材料科学 · 环境科学
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Small Structures · 2026 ·Vol. 7 ·期 3 ·e202500861 · IF 8.9

Dual-Functional 3D-Printed Porous Titanium–Hydrogel Composite Scaffold With Mg2+ and ZIF-8 Release for Enhanced Bone Regeneration and Bacterial Inhibition

Hui Dong,Tongyang Li,Zhen Tang,Dongmei Yu,Cheng Ju,Yiran Zhang,Jia Sha,Yongping Liang,Xinghui Wei,Yichao Liu,Lei Shi,Liang Yan,Hao Wu,Baolin Guo,Zheng Guo

3D-printed titanium implants are extensively utilized in bone reconstruction. However, their bioinertness and lack of antibacterial activity increase risks of aseptic loosening and implant-associated infection—the primary causes of implant failure. To address these limitations, we developed a dual-functional 3D-printed porous titanium–hydrogel composite scaffold to enhance the osteogenic and antibacterial capacities of titanium. This composite scaffold was fabricated by integrating quaternized chitosan (QCS)/aldehyde-terminated Pluronic F127 (PF127-CHO) hydrogel loaded with magnesium ions (Mg 2+ ) and zeolitic imidazolate framework-8 (ZIF-8) into polydopamine-coated 3D-printed porous titanium scaffold. The composite scaffold exhibited sustained and controlled release of Mg 2+ and ZIF-8 with enhanced binding strength at titanium–hydrogel interface. In vitro experiments demonstrated that the composite scaffold possessed favorable biocompatibility, promoted the adhesion and proliferation of MC3T3-E1 cells, and facilitated their osteogenic differentiation through synergistic effect of Mg 2+ and ZIF-8. Furthermore, it also inhibited bacterial growth via synergistic action of QCS/PF127-CHO hydrogel and ZIF-8. In vivo experiments confirmed enhanced bone ingrowth into the composite scaffold and its effective antibacterial activity. In summary, this composite scaffold provides a promising strategy to simultaneously improve the osteogenic and antibacterial capacities of titanium implants.

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THIN SOLID FILMS · 2017 · IF 1.879

A novel bilayer photoanode made of carbon nanotubes incorporated TiO2 nanorods and Mg2 + doped TiO2 nanorods for flexible dye-sensitized solar cells

Lixin Song,Jifeng Zhai,Pingfan Du,Jie Xiong,Frank Ko

TiO 2 nanorods (NRs), Mg 2   + doped TiO 2 (Mg 2   + /TiO 2 ) NRs, and carbon nanotubes incorporated TiO 2 (CNTs/TiO 2 ) NRs are fabricated from the corresponding electrospun nanofibers (NFs) by ultrasonic treatment , respectively. Then these NRs are made into various photoanodic films through electrospray deposition and hot-compression for flexible dye-sensitized solar cells (FDSSCs). The conversion efficiency of FDSSCs is improved with the CNTs incorporation or the Mg 2   + ions doping of TiO 2 . To further improve the properties of FDSSCs, various bilayer photoanodic films made of the smaller diameter NRs as under-layer and the larger diameter NRs as over-layer are prepared. Finally, a highest conversion efficiency of 3.9% is obtained using the bilayer NRs film composed of the smaller diameter CNTs/TiO 2 NRs and the larger diameter Mg 2   + /TiO 2 NRs. This efficiency is much higher than that of the single-layer NRs film based FDSSCs. This may be attributed to the increased light harvesting resulting from the scattering layer of the larger diameter NRs and the faster electron transport due to the two-level energy steps of the bilayer NRs film.

研究领域: 材料科学 · 纳米技术 · 光伏学 · 能源材料
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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

A nanofiltration membrane with positively and negatively charged groups by grafted p-aminosalicylic acid-Fe(III) chelation for Li+/Mg2+ efficient separation

Yanghe Liu,Quan Li,Shenghuan Wang,Mengzhu Liang,Yanhong Ji,Zhenyu Cui,Mohammad Younas,Jianxin Li,Benqiao He

High-performance nanofiltration (NF) membrane plays a key role in Li + /Mg 2+ separation process. In this work, a new NF membrane with positively and negatively charged groups was prepared by grafting p-aminosalicylic acid (AS) onto the surface of polyamide (PA) membrane followed by chelation with Fe 3+ ions for Li + /Mg 2+ separation. The AS grafting (PA-g-AS) and Fe 3+ chelating (PA-g-AS-Fe) NF membranes had almost same surface and section structure and surface pore size as the PA membrane. But Zeta potential (about −8 mV at pH 7) of the obtained PA-g-AS-Fe membrane was improved in comparison with the PA and PA-g-AS NF (about −20 mV at pH 7) membranes due to Fe 3+ addition, suggesting that there were positively and negatively charged groups on the membrane surface. The PA-g-AS-Fe membrane showed a high Mg 2+ rejection of 97.7% and high Li + permeation (negative rejection of −87.6%); while a high Li + /Mg 2+ separation factor (S Li , Mg ) of about 81.5 was achieved, which is much higher than those for PA and PA-g-AS NF membranes and surpassed those of the results reported in literature. The fluxes of three membranes were about the same. The results demonstrated the NF membrane with positively and negatively charged groups was suitable for efficient separation of Li + /Mg 2+ and would have promising applications in recovery of lithium from brine.

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JOURNAL OF LUMINESCENCE · 2021 · IF 3.599

Artificial mimics of light-harvesting organic pigment via a double-perovskite structure (LiLa2SbO6:Bi3+, Mg2+, Mn4+) with single-composition and structure-activity relationship

Qijian Zhu,Jiansheng Huo,Liguo Zhang,Jinwei Gao,Qianming Wang

Green photosynthetic pigments play a major role in light-harvesting for biological substances and bio-mimetic strategy will provide a structural or functional model for natural antenna system . But the precise supramolecular structure of chlorosome has still not been clearly identified and the simulation of its function with new alternatives will be a real challenge. It has been well accepted that blue and far-red light are responsible for photosynthesis and photomorphogenesis in the process of plant growth. In this work, a series of single-composition LiLa 2 SbO 6 (abbreviated as LLSO): x Bi 3+ , y Mg 2+ , z Mn 4+ phosphors with double perovskite‐type structure and the evaluation as blue and far-red dual-emission light for plant growth light-emitting diodes (LEDs) have been reported via a high-temperature solid-state reaction method. Under near ultraviolet-light ( n -UV) excitation at 355 nm, intense blue emission (ranging from 360 to 500 nm, 3 P 1 → 1 S 0 ) from Bi 3+ and far-red emission (650–750 nm, 2 E g → 4 A 2g ) from Mn 4+ are found in Bi 3+ -Mn 4+ co-activated LLSO phosphors. To further optimize the photophysical properties, smaller Mg 2+ has been incorporated into Li  +  site in Bi 3+ -doped LLSO phosphor to control blue emission of Bi 3+ . With the increase of Mg 2+ content, an obvious red shift (~15 nm) of Bi 3+ emission band has been detected in the blue region, which is almost overlapped with the absorbance of Chlorophyll- B (around 450 nm). Moreover, the photoluminescence (PL) emission intensity and decay lifetime of Bi 3+ can be improved by substituting Mg 2+ for Li + . These changes should be attributed to the combined effects of the crystal field splitting and the superior lattice rigidity . Finally, the temperature-dependent PL spectra of the composition-optimized phosphor are measured, and the excellent thermal-stable emission (up to 473 K) has been obtained. It has been observed that Bi 3+ blue emission and Mn 4+ far-red emission exhibit different temperature quenching effect and such phosphor can be considered as an ideal candidate in optical thermometry.

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DESALINATION · 2026 · IF 9.9

Layer-by-layer assembly of polycationic electrolytes onto cation exchange membranes for enhanced Li+/Mg2+ selectivity: A comparative study of polyethyleneimine and chitosan

Jiadi Ying,Zhen Cui,Xiaoxiang Xi,Junwei Zhu,Tiancun Liu,Song Lu,Qi Shen,Min Guo,Yeqing Wang,Zhen Yang,Yaochun Chen,Minfeng Zeng,Zhixin Yu,Yuqing Lin

The selective separation of Li + from Mg 2+ in salt lake brines is critical for sustainable lithium supply but remains challenging due to their similar hydrated radii. Unlike conventional approaches that rely on a single polyelectrolyte system, this study introduces a comparative layer-by-layer (LbL) assembly strategy to systematically screen optimal polycationic building blocks. We employ two distinct polycations, polyethyleneimine (PEI) and chitosan (Cs), paired with poly(sodium 4-styrenesulfonate) (PSS) on a sulfonated poly(ether ether ketone) (SPEEK) substrate, and systematically elucidate how polycation chemistry governs membrane structure, surface charge, and ion-transport behavior across the entire LbL assembly series. The optimized PEI7.5 membrane delivers a Li + /Mg 2+ permselectivity of 9.7, a 13-fold improvement over pristine SPEEK (0.73) and a 31% enhancement over Cs7.5 (7.4), while maintaining a high Li + flux of 0.22 mol·m −2 ·h −1 . This performance represents one of the highest selectivity values reported for LbL-assembled monovalent cation exchange membranes. Combined experimental characterization and molecular dynamics simulations reveal that the superior performance of PEI-based membranes originates from synergistically enhanced denser positive charge sites and narrower pore size distribution, which collectively impose stronger electrostatic repulsion and steric hindrance against Mg 2+ . Overall, this work not only establishes a robust structure–property relationship for LbL-assembled polyelectrolyte membranes, but also provides a polycation-screening paradigm and a mechanistic framework for rationally designing next-generation cation exchange membranes toward high-efficiency lithium extraction from brines.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2024 · IF 7.7

Multi-DNAzymes cascade reaction mediated aptasensors for OTA detection based on the integration of autocatalytic Mg2+-dependent DNAzyme cleavage and entropy-driven circuit

Wenshan Li,Qingqing Li,Huaiyue Xia,Wenjie Liu,Guoxing Jing,Jianna Yu,Wen Liu,Mengtong Lin,Yujuan Huang

Ochratoxin A (OTA) is a compound of concern due to its potential health effects on humans. Detecting OTA in food is crucial for safeguarding public health. In this study, we fabricated a multi-DNAzyme cascade reaction-mediated colorimetric aptasensors for OTA detection, integrating autocatalytic Mg 2+ -dependent DNAzyme cleavage (MNAzyme) and an entropy-driven circuit. In brief, the recognition between the aptamer and target OTA led to the release of DNA1. Subsequently, DNA1 hybridized with DNA2, generating an upstream MNAzyme that facilitated the production of a downstream MNAzyme. These MNAzymes possess similar substrate binding arms, enabling them to catalyze the same substrate. The catalytic efficiency of MNAzymes towards the substrates was enhanced due to the increasing concentration of MNAzymes. The cleavage products then triggered an entropy-driven cycle to generate a signal. Under optimal conditions, the sensing system exhibited low detection limits of 48.97 fM for OTA. Additionally, the proposed aptasensor was successfully applied to quantitatively analyze OTA in food samples. Thus, the multi-DNAzyme cascade reaction-mediated colorimetric aptasensors offer an adaptable platform for detecting traces of OTA contaminant in food.

CAS / MDL: 30931-67-0
研究领域: 食品安全检测 · 分子生物学
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ENERGY & FUELS · 2024 · IF 5.2

Mg2+/S Co-Decorated V, O Sites to Construct Multi-Defect V2O5 as a Sulfur-Wrapped Matrix for High-Performance Lithium–Sulfur Batteries

Lan Li,Tingxue Fang,Fuming Lai,Xinyue Li,Tingting Qu,Lin Wang,Xiaoshi Lang,Kedi Cai

Vanadium pentoxide (V2O5) is regarded as a promising sulfur-wrapped matrix for high-performance lithium–sulfur batteries, owing to its desirable structural and functional characteristics. In this paper, a large number of defective sites arise in the vanadium pentoxide structure via a codecoration strategy of the V, O sites, which is more beneficial to improving the electroconductivity and allows for the uniform loading of sulfur on the surface, thereby reducing the polarization resistance and elevating the kinetic rates during the electrochemical reaction. Electrochemical test results indicate that Mg2+/S-codecorated V2O5/S composite cathodes have 1131.15, 942.39, and 804.71 mAh·g–1 of discharge-specific capacities at 0.1, 0.2, and 0.5 C rates, respectively, with the lowest charge/discharge plateau voltage difference, and the capacity retention rate after 140 cycles can be 57.95%. Besides that, the multidefect V2O5 can effectively promote the adsorption strength of lithium polysulfide and catalytically accelerate the rate of liquid-phase conversion between lithium polysulfide so as to achieve the stable electrochemical properties for sulfur composite cathodes.

CAS / MDL: 7803-55-6
研究领域: 材料科学 · 电化学
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Journal of Materials Research and Technology-JMR&T · 2023 · IF 6.4

Effect of La3+ and Mg2+ combined system on bioactivity and osteogenesis of bioinspired La-doped magnesium phosphate composites prepared utilizing the precursor method

Qiaoyun Liu,Yifeng Yu,Changjiang Liu,Yuhang Liu,Liangjie Yuan,Zheng Wang,Aixi Yu

Lanthanum (La) compounds have attracted much attention because of low toxicity and biocompatibility. In this study, a series of La-doped magnesium phosphate composites bone repair materials (LMPCs) were prepared by the precursor method, in which the molar ratio of lanthanum was 1%, 3% and 5%, respectively. The results of X-ray powder diffraction, scanning electron microscope and compressive strength test show that La-doped magnesium phosphates (LMPs) synthesized by the precursor method have uniform particle distribution, high purity and excellent degradability. In vitro research results show that LMPCs exhibited reliable biosafety and excellent bioactivity. The introduction of lanthanum enhances the antibacterial activity of Escherichia coli and Staphylococcus aureus of the composite. Furthermore, the combined system of released La 3+ and Mg 2+ is more conducive to promoting the proliferation of mesenchymal stromal cells (MSC) and angiogenesis of human umbilical vein endothelial cells (HUVECs) when the content of lanthanum is 3% (referred to as LMPC-2). By up-regulating the expression of alkaline phosphatase (ALP) and Runt-related transcription factor 2 (RUNX2), LMPC-2 is prominent in promoting osteogenic differentiation, and mineralized calcium deposition in vitro . Moreover, the results of micro-CT, H&E and Masson staining confirmed the beneficial effect of the combined system of La 3+ and Mg 2+ on the repair of rat skull defects in vivo . These achievements will provide new strategies for improving the biological activity of LMPCs and provide reference value for bone repairing in the clinic.

CAS / MDL: 54451-24-0 1309-42-8
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Chemical Science · 2020 ·Vol. 11 ·期 7 ·1948-1956 · IF 9.346

Capture and selective release of multiple types of circulating tumor cells using smart DNAzyme probes

Qianying Zhang,Wenjing Wang,Shan Huang,Sha Yu,Tingting Tan,Jian-Rong Zhang,Jun-Jie Zhu

The effective capture, release and reanalysis of circulating tumor cells (CTCs) are of great significance to acquire tumor information and promote the progress of tumor therapy. Particularly, the selective release of multiple types of CTCs is critical to further study; however, it is still a great challenge. To meet this challenge, we designed a smart DNAzyme probe-based platform. By combining multiple targeting aptamers and multiple metal ion responsive DNAzymes, efficient capture and selective release of multiple types CTCs were realized. Sgc8c aptamer integrated Cu2+-dependent DNAzyme and TD05 aptamer integrated Mg2+-dependent DNAzyme can capture CCRF-CEM cells and Ramos cells respectively on the substrate. With the addition of Cu2+ or Mg2+, CCRF-CEM cells or Ramos cells will be released from the substrate with specific selectivity. Furthermore, our platform has been successfully demonstrated in the whole blood sample. Therefore, our capture/release platform will benefit research on the molecular analysis of CTCs after release and has great potential for cancer diagnosis and individualized treatment.

研究领域: 生物技术 · 癌症研究 · 分子生物学
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JOURNAL OF LUMINESCENCE · 2023 · IF 3.6

Achieving the performance luminescence of LaMg0.5Sn0.5O3:Cr3+ by [In3+-Sc3+] co-substitution [Mg2+-Sn4+] and its application to the biodetection and night vision lighting

Bingkai Gao,Lei Zhang,Runqiu Peng,Panlai Li,Qian Wu,Zhijun Wang

The exploration of performance luminescence near-infrared (NIR) material is crucial for rapidly developing NIR spectroscopic techniques. Herein, the NIR LaMg 0.5 Sn 0.5 O 3 :Cr 3+ phosphor was synthesized by a high temperature solid-state method. And its luminescence performance were improved by [In 3+ -Sc 3+ ] substituting for [Mg 2+ -Sn 4+ ]. The half-peak width can be expanded to 211 nm, the emission intensity can reach the seven times of that un-substitution, and the emission intensity at 423 K was maintained at 60 % of that at room temperature , moreover, the internal quantum efficiency can reach 54.2 %. On this basis, the phosphor converted light emitting diodes ( pc -LEDs) were achieved by combining La(Mg 1-x Sn 1-x In x Sc x ) 0.5 O 3 :Cr 3+ with blue LED, importantly, it can be applied to the biodetection and night vision lighting, which indicate its application value.

研究领域: 材料科学 · 生物医学工程 · 光学材料 · 分子影像 · 转化医学 · 光电子学
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