JOURNAL OF NANOPARTICLE RESEARCH
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2021
·Vol. 23
·期 7
·1-14
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IF 2.253
Yu Linkang,Lin Runlian,Han Yu,Fan Dehui,Zhou Guoqiang,Zhang Jinchao,Jia Guang,Ge Kun
With the wide use of rare earth nanomaterials in industry, environmental control, and medicine with their unique properties, it has focused on the exposure of humans to the rare earth nanoparticles in recent years. Because of the similar properties of rare earth and calcium, rare earth nanoparticles can deposit in the bone and affect the osteogenic differentiation of bone mesenchymal stem cells (BMSCs). La(OH) 3 nanoparticles are widely used in the catalysis, sensor, electrode, and luminescent materials. However, there are few reports about the bioactivity of La(OH) 3 nanoparticles on the bone metabolism. In this work, three La(OH) 3 nanorods have been got by hydrothermal method, Long-, Medium-, and Short-La(OH) 3 nanorods, the lengths of which were of ~ 640, 255, and 80 nm, and the diameters of which were of ~ 85, 40, and 35 nm, respectively. All the La(OH) 3 nanorods showed no effect on BMSCs viability and the blood compatibility. But the osteogenic differentiation showed a significant difference in La(OH) 3 nanorods, in which Short-La(OH) 3 nanorods showed the highest promoting effect on osteogenic differentiation. The potential mechanism in the osteogenic differentiation caused by three La(OH) 3 nanorods was correlated with the different uptake efficiency in BMSCs and degradation in lysosome to form LaPO 4 . This work on La(OH) 3 nanorods provides the basic data for the development of lanthanum-based nanoparticles. Graphical abstract
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GREEN CHEMISTRY
·
2015
·Vol. 17
·期 5
·2888-2895
·
IF 8.02
Jian-hua Guo,Guang-yue Xu,Fei Shen,Yao Fu,Ying Zhang,Qing-xiang Guo
The long-chain alkanes obtained from the hydrodeoxygenation of plant oils are ideal substitutes for diesel. In this work, a new efficient catalytic system was established for the conversion of plant oil to long-chain alkanes under mild conditions with a bi-functional Ru/La(OH)3 catalyst. The hydrodeoxygenation of stearic acid was performed in an autoclave with Ru-based catalysts with different supports (HZSM-5, ZSM-5, SiO2–Al2O3, SiO2, ZrO2, Mg(OH)2, La(OH)3, and La2O3). Among these catalysts, Ru supported on basic La(OH)3 showed a remarkable catalytic performance for the reaction. Over 98% of long-chain alkanes were obtained with 100% conversion of stearic acid at 200 °C and 4 MPa H2. When crude Jatropha oil was hydrogenated, about 80.7 wt% of long chain alkanes were obtained under the optimized conditions (200 °C, 4 MPa H2, 8 h). The high efficiency of the Ru/La(OH)3 catalyst could be due to a co-effect of the high hydrogenation activity of Ru and the basic La(OH)3 support which can attract the acidic raw material. Additionally, the Ru/La(OH)3 catalyst was recycled four times and maintained a good activity and stability. The reaction pathway was also explored by using stearic acid as a model compound. Hydrogenation–decarbonylation could be the main pathway to produce n-heptadecane, which has one carbon atom less than stearic acid.
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International Journal of Electrochemical Science
·
2024
·
IF 1.3
Dandan Liang,Weili Hou,Ying Zhang,Jihua Shang,Haibo Ren,Yufeng Sun
Due to the prevailing energy shortages, the pursuit of new alternative energy sources is becoming increasingly urgent. Hydrogen production through water electrolysis has emerged as a crucial method. However, the sluggish four-electron reaction in the oxygen evolution reaction (OER) remains the primary rate-limiting step. In this study, we synthesized a heterostructure La(OH) 3 @CuO-P material on the nickel foam (NF) substrate. The experimental results demonstrate that after phosphating treatment, the heterostructure La(OH) 3 @CuO-P exhibits exceptional catalytic performance with only 215 mV overpotential, a Tafel slope value of 79.36 mV/dec, and a bilayer capacitance of 39.02 mF/cm 2 at a current density of 10 mA/cm 2 for OER in a 1 M KOH solution. These values are significantly superior compared to those obtained using heterostructure La(OH) 3 @CuO alone which showed an overpotential value of 365 mV at a current density of 10 mA/cm 2 . Moreover, during cyclic voltammetry testing for up to 500 cycles, La(OH) 3 @CuO-P also demonstrates relatively stable performance. Analyses suggest that composite heterostructure effectively addresses issues such as insufficient conductivity of La(OH) 3 and monomer aggregation tendency for CuO while maintaining excellent properties for each component. By incorporating P atoms as dopants, the interaction between La, Cu, and P atoms not only facilitates fine-tuning of the electronic structure and optimization of the adsorption free energy (-OH), but also promotes an increase in catalytic active sites through sample size reduction, thereby further augmenting the performance of the OER.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2020
·
IF 4.939
Hongtao Zou,Feng Guo,Minghong Luo,Qilu Yao,Zhang-Hui Lu
Ultrafine NiFe nanoparticles (NPs) decorated by La(OH) 3 have been successfully prepared via a facile one-step co-reduction method without the help of surfactant or support. It was found that after being decorated with La(OH) 3 , the NiFe–La(OH) 3 NPs have a smaller particle size and lower crystallinity . The resultant NiFe–La(OH) 3 nanocatalyst exhibits an excellent catalytic activity , 100% H 2 selectivity, and satisfied recyclability for hydrogen evolution from hydrous hydrazine (N 2 H 4 ·H 2 O) at 343 K under alkaline conditions, giving a high turnover frequency (TOF) value of 100.6 h −1 , which is more than 35 times higher than pure NiFe NPs (2.8 h −1 ). The kinetics study shows that with respect to the concentration of catalyst and N 2 H 4 , the N 2 H 4 dehydrogenation reaction follows fist-order kinetics and zero-order kinetics, respectively. Furthermore, NiFe–La(OH) 3 also exhibits an outstanding performance and excellent recycle stability during high dehydrogenation of hydrazine borane (N 2 H 4 BH 3 ). The excellent performances for the dehydrogenation of N 2 H 4 and N 2 H 4 BH 3 could be attributed to the strong interaction between La(OH) 3 and NiFe NPs, as well as ultrafine and low crystalline NiFe NPs due to the addition of La(OH) 3 .
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Surfaces and Interfaces
·
2026
·
IF 6
Hui Zhou,Bingxin Zhu,Xiang Li,Baolei Liu,Zhigang Liu,Shihua Yu
To recover the high value-added pharmaceutical intermediate tenofovir from wastewater efficiently and conveniently, a tailored magnetic composites of Fe 3 O 4 @SiO 2 @La(OH) 3 have been prepared via solvothermal and in-situ reduction methods. It exhibits the ability to remove tenofovir with high efficiency and easily separated from matrix. Batch sorption experiments demonstrated that Fe 3 O 4 @SiO 2 @La(OH) 3 can remove tenofovir with the maximum adsorption capacity of 64.53 mg/g, the largest removal of 93.07%, and fast equilibrium time of 5 min. The kinetics of tenofovir adsorption on the magnetic composite is in line with the pseudo-second-order model, while the isotherm is fitted well by the Langmuir model, and thermodynamic parameters represent that adsorption process is spontaneous and endothermic. Moreover, the saturated Fe 3 O 4 @SiO 2 @La(OH) 3 have been desorbed by mechanical stirring with the high desorption rate of 93.02%, and the adsorption capacity maintaining 47.72 mg/g after five cycles. Importantly, the composites can be used for tenofovir removal from crude extracts of pharmaceutical wastewater, with an adsorption capacity of 51.61mg/g in 5 min. Finally, the adsorption mechanisms are explored by pH experimental evidence and XPS analysis, which show that mainly involve electrostatic attraction and the inner-sphere complexation between La(OH) 3 and phosphate groups of tenofovir via ligand exchange. All the results prove that the proposed tenofovir recovery technique, providing new ideas for the recovery of high value-added substances and waste resources rationalization of the application of development. A magnetic Fe 3 O 4 @SiO 2 @La(OH) 3 was synthesized and realized the recovery of tenofovir with high economic value in pharmaceutical wastewater crude extracts. Download: Download high-res image (249KB) Download: Download full-size image
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Journal of Cleaner Production
·
2023
·
IF 11.1
Yicong Wang,Sisuo Zhang,Richard L. Smith,Xiaoning Liu,Xinhua Qi
Effective removal of both nitrogen and phosphorus from water is of great importance for maintaining the safety of the environment. In this work, ordered mesoporous carbon electrode materials containing La(OH) 3 and Fe 3 C components (La#OMC-Fe 3 C) were prepared by combining solvent evaporation induced self-assembly and impregnation methods. The ordered pores in La#OMC-Fe 3 C facilitated electron transfer at the electrode-solution interface during nitrate reduction and provided voids for phosphate removal . In the electrochemical system, Fe 3 C in the electrode supplied electrons for nitrate reduction and gave the electrode a high degree of stability, whereas La(OH) 3 selectively removed phosphate, thus avoiding byproduct precipitation from solution. The electrode material maintained efficient electrochemical nitrogen and phosphorus removal over a wide range of conditions including pH (3–11) and aqueous environments containing multiple ions (Cl − , SO 4 2− , K + , Na + , Ca 2+ , Mg 2+ ) or actual aqueous environments (seawater). After 10 cycles, the performance of La#OMC-Fe 3 C for nitrogen and phosphorus removal remained above 97%. This work realizes the simultaneous removal of nitrogen and phosphorus in the electrochemical system, and solves the problems of precipitation in water and non-circulation of electrodes, which can provide a new strategy for the treatment of eutrophic water in practical production.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2022
·
IF 8.025
Debin Jiang,Xiaoping Wang,Li Feng,Yichang Yu,Jie Hu,Xiaoying Liu,Hong Wu
In this study, a novel nano-La(OH) 3 /porous carbon composites derived from La alginate xerogel with egg-box structure had been successfully synthesized by a gradient heat treatment in nitrogen atmosphere. This facile fabrication strategy can be easily employed to considerably encapsulate La(OH) 3 nanoparticles uniformly into the porous carbon matrix derived from the alginate macromolecule framework. The optimized sample, labeled as LS-550(N), exhibited extremely high phosphate uptake and great selectivity. The adsorption kinetic process dramatically followed pseudo-second-order model. The Langmuir model fitted maximum equilibrium adsorption capacity is 133.58 mg·g −1 . The phosphate adsorption mechanisms could be consist of electrostatic interaction, complexation and ligand exchange interaction on the surface of LS-550(N). The prominent practical applicability of LS-550(N) in the regeneration test suggests that the LS-550(N) could be a potential adsorption candidate for the decontamination of phosphate-containing natural water bodies.
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PubMed
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Desalination and Water Treatment
·
2024
·
IF 1
Yuhang Xu,Wei Li,Sisi Qin,Kai Su,Junmin Chen,Shengli Zhang
ABSTRACT In this study, La(OH) 3 -loaded Juncus effusus (La-JE) with a three-dimensional structure was prepared via an in-situ precipitation and then wrapped in a cellulose membrane. The La-JE not only avoided the leakage of La(OH) 3 but also was separated from solution easily. The optimal pH for phosphate removal by the La-JE was 6. The removal rate of phosphate was positively correlated with adsorption time, La-JE dosage and reaction temperature, and negatively correlated with phosphate concentration. The adsorption process conformed to pseudo-second-order kinetic model and was better fit by Freundlich model. At 25°C, the maximum adsorption capacity of the La-JE was 22.75 mg·P/g. The influence of SO 4 2– , Cl – , NO 3 – , NH 4 + , HCO 3 – and CO 3 2– on phosphate removal was negligible, suggesting that the La-JE had good anti-interference ability. Mechanism analysis showed that the removal process of phosphate was related to both ligand exchange and surface precipitation. The application in real water environment exhibited that the La-JE had good potential for advanced dephosphorization of sewage treatment plant and natural waterbody remediation.
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ACS Nano
·
2015
·
IF 12.881
Jiaojie He,Wei Wang,Fenglian Sun,Wenxin Shi,Dianpeng Qi,Ke Wang,Ruisha Shi,Fuyi Cui,Ce Wang,Xiaodong Chen
La(OH)3 nanorods immobilized in polyacrylonitrile (PAN) nanofibers (PLNFs) were fabricated for the first time by electrospinning and a subsequent in situ surfactant-free precipitation method and then applied as a highly efficient phosphate scavenger to realize nutrient-starvation antibacteria for drinking water security. The immobilization by PAN nanofibers effectively facilitated the in situ formation of the aeolotropic and well-dispersed La(OH)3 nanostructures and, thus, rendered higher phosphate removal efficiency due to more exposed active sites for binding phosphate. The maximum phosphate capture capacity of La(OH)3 nanorods in PAN nanofibers was around 8 times that of the La(OH)3 nanocrystal fabricated by precipitation without PAN protection. Moreover, remarkably fast adsorption kinetics and high removal rate were observed toward low concentration phosphate due to the high activity of our materials, which can result in a stringent phosphate-deficient condition to kill microorganisms in water effectively. The present material is also capable of preventing sanitized water from recontamination by bacteria and keeping water biologically stable for drinking. Impressively, stabilized by PAN nanofibers, the La(OH)3 nanorods can be easily separated out after reactions and avoid leaking into water. The present development has great potential as a promising antimicrobial solution for practical drinking water security and treatment with a negligible environmental footprint.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2024
·
IF 8.1
Kelin Li,She Chen,Mengbo Li,Linlin Liu,Yunjie Li,Feng Wang
Ammonia is a promising carrier for energy storage due to its high hydrogen content, low storage and transportation costs, and zero carbon emissions. Plasma catalysis shows excellent potential for sustainable ammonia synthesis; however, searching for suitable catalysts is ongoing. La(OH) 3 was studied due to its rich basic sites and oxygen vacancies, which are beneficial for plasma-catalyzed ammonia synthesis. The optimal reaction conditions were investigated, and a maximum ammonia synthesis rate of 37.13 μmol/(min•g -cat ) was achieved. H 2 plasma treatment enhanced the catalytic activity of La(OH) 3 , and ammonia synthesis rate of 40.00 μmol/(min•g -cat ) were achieved. This study contributes to the development of efficient catalysts for plasma-catalyzed ammonia synthesis and highlights the potential of La(OH) 3 as a promising catalyst.
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CHEMICAL PHYSICS LETTERS
·
2019
·
IF 1.901
Zhuo Zhou,Haiming Xu,Dongya Li,Zhongwei Zou,Dongsheng Xia
La(OH) 3 /BiOCl n-n heterojunction (BCL) was successfully fabricated by facile microwave technique. Photocatalytic performance experiments confirmed that BCL-20 can degrade 20 mg/L tetracycline hydrochloride (TC-HCl) about 85% in 60 min, which is 2 and 0.5 times higher than that of BiOCl and La(OH) 3 , respectively. The photocatalytic mechanism reveals that the co-effect of oxygen vacancies (OVs) and rebuilt internal electric field induced by heterostructure not only broaden the light-responsive range but also augment the separation efficiency of photogenerated carriers, thus improving the photocatalytic properties of BCL. This work provides a new avenue for improving the photocatalytic performance of Bi-based photocatalysts by heterojunction and OVs.
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Journal of Environmental Chemical Engineering
·
2025
·
IF 7.2
Suyu Kong,Meili Ding,Mengjiao Yu,Wei Rong,Yang Wang,Jianfeng Yao
Developing high-efficiency adsorbents with sufficient active species to remove phosphate from wastewater is still a significant and formidable challenge. Herein, a metal-ion modification strategy was developed to construct a series of lanthanum (La 3 + )-functionalized zirconium-based metal-organic frameworks containing different functional groups through a one-step solvothermal process. The investigations for the influence of functional groups of ligands on the resulting La species and the role of La(OH) 3 in the phosphate removal are the primary focuses of this research. Unlike the simple La doping in UiO-66, UiO-66-NH 2 and many previously reported MOF systems, La(OH) 3 was in situ formed during the preparation of La-functionalized UiO-66-OH, which was confirmed by powder X-ray diffraction. At room temperature, the optimized 0.5La-UiO-66-OH, with a molar ratio of La 3+ versus the total metal precursor of 0.5, exhibits a desirable adsorption capacity of 219.6 mg g −1 , exceeding those of UiO-66 (146.8 mg g −1 ), UiO-66-OH (158.9 mg g −1 ), and many reported adsorbents. Besides, reusability tests demonstrate that 0.5La-UiO-66-OH can maintain high adsorption performance (96 %) after five cycles and the practical usability of by 0.5La-UiO-66-OH is confirmed using real lake water. In-depth investigations (X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy) on mechanism unveiled that the adsorption of phosphate by 0.5La-UiO-66-OH involved a combined process of electrostatic attraction and ligand exchange. This research presents the first regulation of generating active La species within MOFs through subtle modification and provides valuable insights for wastewater treatment.
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