TALANTA
·
2024
·
IF 5.6
Dandan Guo,Diya Zheng,Ding Zhou,Changlun Tong,Shaohua Huang
Lysine (Lys) is an essential nutrient that plays a crucial role in the growth and development of living organisms. Chiral analysis of Lys holds significant importance for ensuring the safety of food, pharmaceuticals, and health products. In this work, an achiral Zr-based metal organic frameworks (MOFs), UiO-66-NH 2 , was proposed as a fluorescent probe to achieve rapid response to l -lysine (L-Lys) in solution. Additionally, Zr 4+ in the skeleton of UiO-66-NH 2 framework exhibited different binding capacities towards Lys enantiomers, leading to distinct fluorescence responses for L-Lys and d -lysine (D-Lys). Leveraging these properties, the UiO-66-NH 2 probe enabled accurate determination of L-Lys concentrations in solution, as well as the enantiomeric excess (ee) values of Lys solutions. Notably, in the detection of Lys enantiomers, the achiral UiO-66-NH 2 acted as both a chiral selector and a fluorescent indicator, greatly improving the efficiency and stability of the detection system. The probable mechanism was further elucidated by pH titration experiments and density functional theory calculations. Additionally, the general applicability of this mechanism was validated by similar amino MOFs. The application of the UiO-66-NH 2 fluorescent probe in analysis of infant formula milk powders and liquid milk samples confirmed the reliability of the method. Moreover, the construction of fluorescence test paper by immobilizing UiO-66-NH 2 onto filler papers enabled the rapid identification of Lys enantiomers. Compared to previous fluorescent analyses of chiral amino acids assisted by additional metal ions, this study presented a novel approach and methodology that offers high efficiency, stability, reproducibility and reusability for the identification and detection of Lys enantiomers, highlighting the potential of the UiO-66-NH 2 fluorescent probe in advancing analytical techniques.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Yong Tang,Jianhao Qiu,Dingliang Dai,Guanglu Xia,Biyao Fang,Yixin Li,Jianfeng Yao
Defect engineering is used in the development of photocatalysts and has received widespread attention for achieving efficient photocatalysis. Here, ZnIn 2 S 4 with rich sulfur vacancies (V S -ZnIn 2 S 4 ) was integrated with MIL-53-NH 2 for photocatalytic H 2 O 2 production from O 2 reduction under visible light. The sulfur vacancy could effectively promote charge separation and O 2 capture, and the heterostructure between ZnIn 2 S 4 and MIL-53-NH 2 further inhibits charge recombination, which promises highly boosted photocatalytic activities. In ambient air and pure water, V S -ZnIn 2 S 4 /MIL-53-NH 2 heterostructures exhibit superior photocatalytic H 2 O 2 production performance (705 μmol·L −1 ) relative to those of monomeric Znln 2 S 4 (78 μmol·L −1 ), V S -Znln 2 S 4 (210 μmol·L −1 ), MIL-53-NH 2 (38 μmol·L −1 ), as well as ZnIn 2 S 4 /MIL-53-NH 2 (395 μmol·L −1 ). Mechanistic studies have confirmed that the main pathway for H 2 O 2 formation on V S -ZnIn 2 S 4 /MIL-53-NH 2 is ⋅O 2 – -triggered O 2 reduction, and sulfur vacancy can adsorb and activate O 2 to facilitate the production of ⋅O 2 – . This study provides new insights into catalyst design and green synthesis of H 2 O 2 .
✓ 已验证
产品关联
DOI
高影响因子
CATALYSIS LETTERS
·
2025
·Vol. 155
·期 2
·1-18
·
IF 2.4
Xu Lingling,Pan Xiaomei,Gao Lijing,Wei Ruiping,Li Jihang,Wen Xiu,Li Yuanzhuang,Xiao Guomin
UiO–66–NH 2 (Ti/Zr) modified by Ti metal oxide (TiO 2 ) was used to catalyze the hydrolysis of cellulose to prepare 5-HMF. Under the optimal reaction conditions of H 2 O(NaCl)/THF(1/4 mL), 190 °C, 2 h and 50 mg UNT-3(Ti/Zr) (TiO 2 and UiO–66–NH 2 with mass of 1.5 and 0.1 g, respectively), the yield of 5-hydroxymethylfurfural reached 59.88%. UiO–66–NH 2 (Ti/Zr) nanocomposites with different mass ratios were successfully prepared by simple solvent evaporation method. SEM and TEM have shown that the modified UiO–66–NH 2 (Ti/Zr) are wrapped into sphere by TiO 2 densely attached to the surface of UiO–66–NH 2 , which provides favorable conditions for the uniform dispersion of TiO 2 and coordination of the Lewis acidic site of UiO–66–NH 2 . NH 3 –TPD results confirmed the existence of super-strong, strong, middle and weak acid sites in UiO–66–NH 2 (Ti/Zr), and Py-FTIR confirmed the existence of Brønsted and Lewis acids. After four cycles, the yield of 5-HMF and FUR decreased slightly from 59.88 to 51.89% and 9.11 to 7.66%, respectively, and the yield of 5-HMF could still remain above 50%. The results showed that the modified composite treatment of TiO 2 with rich Lewis acid/base and UiO–66–NH 2 could provide a certain idea for the extensive application of biomass research in the future. Graphic
✓ 已验证
产品关联
DOI
高影响因子
ACS Sustainable Chemistry & Engineering
·
2025
·
IF 7.3
Xiaoyan Han,Shan Wang,Tingting Cui,Yumin Yang,Haixiang Li,Haiwen Zhang,Huanhuan Zhou,Xiaoxia Li
Aristolochic acid I (AA-I), a known nephrotoxin and carcinogen, is commonly found in certain medicinal plants, posing significant safety concerns. In this work, defect-engineered, molecularly imprinted UiO-66-NH2 was synthesized via a one-pot hydrothermal method using indomethacin (IND) as a green alternative template. The resulting imprinted metal–organic framework effectively mitigates matrix interference, enabling highly selective recognition and the efficient adsorption of AA-I. Structural characterization confirmed that the imprinting process and template removal did not compromise the framework integrity of UiO-66-NH2. Spectroscopic analysis revealed that AA-I recognition was governed by Zr coordination, electrostatic interactions, and spatially confined recognition sites within the porous framework. Density functional theory calculations further elucidated the interaction mechanisms involved in the adsorption process. The imprinted UiO-66-NH2 exhibited a maximum adsorption capacity of 42.74 mg/g and an imprinting factor of 2.48. In real sample analysis, the material achieved recovery rates of 96.7–103.5% and excellent selectivity in Clematis armandii extracts. The adsorption efficiency remained above 80% after five adsorption–desorption cycles, indicating good structural stability and reusability. This work offers a promising and sustainable strategy for improving herbal medicine safety through the rational design of ecofriendly MOF-based adsorbents.
✓ 已验证
产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2025
·
IF 9
Rashida Shahbaz,Tianyou Li,Yongchao Sun,Samrina Sharif,Gaohong He,Canghai Ma
Mixed matrix membranes (MMMs) have emerged as promising materials for hydrogen separation, combining the processability of polymers with enhanced permeability and selectivity offered by inorganic fillers. However, challenges such as filler aggregation and poor polymer-filler interfacial compatibility limit their performance. In this study, amino-modified bimetallic ZIF (Zn/Co-ZIF-NH 2 ) was synthesized and employed as a novel nanofiller to fabricate 6FDA-DAM-based MMMs, aiming to improve interfacial compatibility between the filler and the polymer matrix. The incorporation of Co 2+ ions into ZIF-8-NH 2 introduced a synergistic effect, optimizing the balance between the rigidity and flexibility of metal-to-ligand bond linkage, while amino groups promoted robust interfacial interactions with the polymer matrix. Compared to the pure polymeric membrane, the MMMs incorporating 40 wt% MOF exhibited a significant enhancement in gas permeability, with H 2 permeability rising from 750 to 3273 Barrer and CO 2 permeability increasing from 840 to 2733 Barrer, corresponding to improvements of 336.4 % and 225 %, respectively. Simultaneously, H 2 /CH 4 and CO 2 /CH 4 selectivities increased to 33.7 and 28.1, representing improvements of 88.3 % and 41 % over the pristine polymer. These performance metrics exceed the 2008 Robeson upper bounds, demonstrating the effectiveness of Zn/Co-ZIF-NH 2 nanofillers in overcoming the permeability–selectivity trade-off. This study underscores the effectiveness of amino-modified bimetallic MOFs as advanced fillers for high-performance MMMs, particularly suited for hydrogen purification and CO 2 separation applications.
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2025
·
IF 2.8
Jingguang Wang,Yutao Lin,Tao Wang,Zhenze Xie,Wenxin Guo,Chang Du
Cancer treatment techniques often struggle to simultaneously address the issues of significant impact from cancer heterogeneity, poor resistance to drugs, and non-selective drug toxicity. Therefore, cancer treatment strategies based on nanoplatforms with multiple responsive properties have attracted wide attention due to their broad applicability and minimal side effects on normal cells. Herein, we constructed a nano iron-based metal–organic framework loading Pt and coated with polydopamine (Fe-MOF-NH 2 @Pt@PDA) using the solvothermal method for multimodal cancer therapy. The Pt and Fe could leverage the unique weak acidity and overexpression of hydrogen peroxide in the tumor cell to generate reactive oxygen species (ROS) for chemodynamic therapy (CDT). Additionally, Pt and Fe gave its peroxidase-like activity to produce oxygen, improving the hypoxic environment in the tumor microenvironment. Due to Pt, Fe-MOF-NH 2 @Pt@PDA achieved excellent sonodynamic therapy (SDT) under ultrasound (US) stimulation. Under US, more ROS were generated, enhancing the anticancer effect of CDT. Moreover, Fe-MOF-NH 2 @Pt@PDA produced an excellent photothermal effect under 808 nm near-infrared (NIR) irradiation for photothermal therapy (PTT). Furthermore, Fe-MOF-NH 2 @Pt@PDA exhibited good biocompatibility. Taken together, the nano Fe-MOF-NH 2 @Pt@PDA with synergistic CDT, SDT, and PTT combined treatment was a promising biomaterial for non-invasive clinical cancer therapy.
✓ 已验证
产品关联
DOI
高影响因子
ANALYTICA CHIMICA ACTA
·
2025
·
IF 6
Jiaqi Niu,Jinhui Liu,Ping Guo,Min Du,Wanqing Wu,Ziyang Zhang,Ye Ning,Dedi Zhou,Haidong Cao
As a common contaminating bacterium, Escherichia coli (E. coli) has caused severe harm in various fields such as food, healthcare, and the environment. Traditional detection methods for Escherichia coli, owing to factors like high cost and low efficiency, are unable to meet the detection requirements at the present stage. Therefore, the development of a simple, rapid, and highly efficient detection method for Escherichia coli represents an urgent issue that needs to be addressed promptly. This study focused on the development of a highly selective molecularly imprinted electrochemical sensor for E. coli. Molecularly imprinted polymers (MIPs) were prepared by electropolymerization on the surface of glassy carbon electrode using o-phenylenediamine as the functional monomer, aminated metal-organic frameworks (MOFs) and carbon nanotubes (CNTs) as the composites, and bovine serum albumin (BSA) was added into the polymer film to attenuate the non-imprinting effect. The linear range of the sensor was 10-10 7 CFU/mL and the detection limit was 5.2 CFU/mL. Good recovery rates were shown in real samples of drinking water, milk and orange juice. In addition, the good binding ability of the E. coli template molecule to the functional monomer o-phenylenediamine was verified by molecular docking and molecular dynamics (MD) simulations. This study was able to detect E. coli in 20 min, which provides a more open idea for the application of rapid detection of E. coli on-site, as well as the construction of molecularly imprinted electrochemical sensors and the analysis of the binding mechanism between template molecules and functional monomers.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF SOLID STATE CHEMISTRY
·
2025
·
IF 3.5
Tongxin Xiao,Kangyue Qiao,Guodong Hao,Songyao Du,Yue Wang,Chao Sui
This study employed a solvothermal method to prepare an NH 2 -MIL-101(Fe, Co) bimetallic organic framework composite catalyst aimed at enhancing the photocatalytic reduction performance of Cr(VI). The experimental results show that introducing Co into the single-metal NH 2 -MIL-101(Fe) does not alter the material's octahedral structure. However, the bimetallic synergistic effect shifts the light absorption range to the red end of the spectrum, reduces the bandgap, and significantly improves carrier separation efficiency. Under visible light irradiation, the NH 2 -MIL-101(Fe, 0.15Co) catalyst exhibited outstanding photocatalytic performance, achieving a reduction efficiency of 94.7% for Cr(VI) within 40 minutes and 100% within 50 minutes, with a reaction rate constant 4.7 times that of the single-metal NH 2 -MIL-101(Fe). Free radical capture experiments further revealed that ·O 2 - is the key active species in the Cr(VI) reduction process, while photo-generated holes in the valence band can oxidise OH - to ·OH, synergistically participating in the reaction. Additionally, cyclic stability experiments showed that the catalyst maintained 85.8% reduction efficiency after five cycles, demonstrating excellent stability and practical application potential.
✓ 已验证
产品关联
DOI
高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
·
2025
·
IF 4.7
Jian Luo,Yonghui Lin,Yanfeng Liu,Siliang Wang,Yiduo Chen,Xudong Tian,Weiting Yang,Zhongmin Su
Roxarsone (3-nitro-4-hydroxyphenylarsenic acid, ROX) is easily converted into highly toxic inorganic arsenic compounds, therefore, the development of highly efficient adsorbents for the removal of ROX from wastewater is necessary but remains challenging. In this study, NH 2 -MIL-101 (Fe) was synthesised and modified with TPA-CHO (4-(N, N-diphenylamine) benzaldehyde) to obtain TPA-MIL-101(Fe) with triphenylamine functionalised groups. The modified TPA-MIL-101(Fe) exhibits the very high adsorption capacity (728.2 mg g −1 ) and fast adsorption equilibrium (2 h). The TPA-MIL-101(Fe) showed excellent selectivity, and the adsorption efficiency hardly decreased in the presence of competing ions (Cl − , NO 3 − , SO 4 2− ). The TPA-MIL-101(Fe) showed good adsorption performance for ROX at pH 3–13, with the best performance at pH = 9. In addition, TPA-MIL-101(Fe) was able to remove trace amounts of ROX from actual water samples (<5 mg L −1 ) with an efficiency of 99.46 %, and the remaining ROX content meets the international drinking water standards of the World Health Organization (29 μg L −1 ). The mechanism studies have shown that the Fe-O-As coordination and the π-π stacking interaction between TPA-MIL-101(Fe) and ROX greatly enhance its adsorption performance. In conclusion, this work provides a promising material for effective removal of ROX from the environmental water.
✓ 已验证
产品关联
DOI
高影响因子
LANGMUIR
·
2025
·
IF 3.9
Mingyang Xiong,Yao Zeng,Ruisi Qiu,Hongxing He,Yi Zhang,Zhifeng Nie,Bing Wang
Bisphenol A (BPA) is extensively utilized as an industrial chemical in the production of certain plastics and epoxy resins. They are frequently found in environmental water and have the potential to cause risks to both the environment and human health. To efficiently remove the endocrine disruptor BPA from aqueous solutions, sea urchin-like magnetic material Fe3O4@PDA@NH2-MIL-101 (Fe) was synthesized via hydrothermal methods. Fe3O4@PDA@NH2-MIL-101 (Fe) has excellent adsorption performance, with a theoretical maximum adsorption capacity of 300.47 mg/g for BPA. The adsorption kinetics of BPA by Fe3O4@PDA@NH2-MIL-101 (Fe) followed the pseudo-second-order kinetic model and Liu’s isotherm model. Magnetic separation experiments reveal a high recovery efficiency, maintaining 94.82% of its initial adsorption capacity after five cycles. The primary adsorption mechanisms of Fe3O4@PDA@NH2-MIL-101 (Fe) on BPA included pore filling, hydrogen bonding, π–π interaction, and Lewis acid–base interaction. Additionally, the material showed excellent removal performance of BPA, with a maximum adsorbed amount of 135.27 mg/g for total organic carbon (TOC) in the shale gas fracturing flowback fluid. These findings suggest that Fe3O4@PDA@NH2-MIL-101 (Fe) holds significant potential as an adsorbent for BPA removal from actual wastewater, offering promising prospects for practical applications.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2025
·
IF 9
Xiaolei Cui,Yuchen Cui,Ziang Li,Zixi Kang,Soryong Ryan Chae,Lubomira Tosheva,Hailing Guo
Under industrially conditions (pressures ≥10 bar), polymer membranes usually exhibit poor CO 2 /CH 4 separation performance and limited stability, severely restricting their practical application. Here, we present a materials engineering strategy, in which phenolic resin is in-situ polymerized on the surface of NH 2 -UiO-66 to engineer the MOF-polymer interface, thereby enabling high CO 2 /CH 4 separation performance and excellent structural stability for mixed matrix membranes. The phenolic resin forms a uniform coating (∼10 nm thick) on the porous MOF surface, providing a high-density CO 2 active sites that accelerate CO 2 transport. In addition, due to favorable interfacial interactions between the phenolic resin shell and the polyetherimide matrix, the resulting MMMs exhibit excellent stability under high pressures. Compared to the pristine PEI membranes, the CO 2 permeability and CO 2 /CH 4 selectivity of the optimized 30-RF@NH 2 -UiO-66-PEI membranes are enhanced by 8550% and 1500%, respectively. Under simulated industrial conditions (10/90 CO 2 /CH 4 mixture at 10 bar and 50 °C), the engineered membranes maintain a CO 2 permeability of 6105 Barrer and a CO 2 /CH 4 selectivity of 30.5, demonstrating excellent separation performance. More importantly, the 30-RF@NH 2 -UiO-66-PEI membrane exhibits both scalability (readily extendable to the square-meter level) and cost-effectiveness (∼55 USD per square meter). This work highlights the potential of phenolic resin-modified MOF fillers to enable efficient CO 2 /CH 4 separation under realistic industrial conditions.
✓ 已验证
产品关联
DOI
高影响因子
WATER AIR AND SOIL POLLUTION
·
2025
·Vol. 237
·期 5
·325
·
IF 3
Song Jiacheng,Zhang Ziyang,Dong Shengye,Chen Anxiang,Yu Shouwu,Xiao Shujuan
The high activity and easy recyclability of catalysts are significant challenges in the photocatalytic treatment of wastewater. Combining photocatalytic technology with membrane separation technology to prepare self-cleaning catalytic composite membranes for treating wastewater containing organic pollutants can not only solve the problem of traditional catalyst recovery difficulties but also overcome membrane fouling. In this paper, NH 2 -MIL-88B was modified by introducing citric acid as a ligand construction defect, and NH 2 -MIL-88B-CA (NMB-CA) with better photocatalytic performance was obtained. Then, a thin film nanocomposite (TFN) film with better self-cleaning performance was prepared by covalently bonding the NMB-CA nanocatellite to the active polyamide layer through interfacial polymerization and amidination in Polysulfone (PSF) based membrane. The best-performing TFN-2 membrane has even better fouling resistance, removing 98.1% of tetracycline after 8 cycles, and the water flux of the membrane can still recover to 99% of the initial water flux, demonstrating excellent recyclability. TFN membrane prepared in this paper has unique self-cleaning and anti-pollution characteristics, which provides a new solution for efficient treatment of organic-contaminated water.
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）