MOLECULES
·
2024
·Vol. 29
·期 16
·3873
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IF 4.2
Fuhua Wei,Xue Gong,Qinhui Ren,Hongliang Chen,Yutao Zhang,Zhao Liang
In this study, Co/Cd-MOFs were synthesized via a solvothermal method. The resulting material was subjected to calcination at 900 °C for 2 h and characterized using FT-IR, XRD, and SEM techniques to assess its efficacy in moxifloxacin removal. The experimental findings revealed that the maximum adsorption capacity of Co/Cd-MOFs for moxifloxacin was observed at 350.4 mg/g within a 5 h timeframe. Furthermore, the analysis based on the pseudo-second-order kinetic model demonstrated that the adsorption process adhered to this specific model. Additionally, the adsorption isotherm analysis indicated that Freundlich multilayer adsorption provided the best description of the interaction between moxifloxacin and the Co/Cd-MOF material. These experimental and theoretical results collectively suggest that employing Co/Cd-MOFs as adsorbents holds promise for wastewater treatment applications.
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JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
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2025
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IF 6
Meinan Yang,Nan Wang,Xu Wang,Ruiyong Zhang,Ini-lbehe Nabuk Etim,Mei-E. Yue,Jizhou Duan,Baorong Hou,Wolfgang Sand
Oxygen vacancies can provide active sites for catalysts, promoting catalytic activity. However, there are fewer nanozyme catalysts with oxygen vacancies. In this study, CeO 2 metal–organic framework (CeO 2 -MOF) nanorods with oxygen vacancies are synthesized through a simple hydrothermal and calcination processes. The obtained CeO 2 -MOFs exhibit excellent nanozyme catalytic activity for antibacterial applications. The CeO 2 -MOF nanorods demonstrate intrinsic haloperoxidase-like activity by catalyzing the bromination of organic signaling compounds, outperforming the catalytic properties of pure CeO 2 . The activity of CeO 2 -MOF (6) is the best because of its large specific surface area of 103.638 m 2 /g, surpassing that of CeO 2 at 74.752 m 2 /g. The oxygen vacancies are crucial in regulating the electronic structure of CeO 2 -MOFs, thereby improving the catalytic performance. The experiments of multiple substrates show that CeO 2 -MOF (6) exhibits good stability and recyclability. Additionally, CeO 2 -MOF (6) can catalyze the oxidation of Br - with H 2 O 2 to the corresponding hypobromous acid (HBrO), which exhibits strong antibacterial activity against typical marine bacteria ( Pseudomonas aeruginosa ). This study expands the range of biomimetic enzyme materials. It provides an efficient and green perspective and strategy for developing antibacterial and antifouling biomimetic catalysts, which offers a sustainable alternative for industrial applications in marine coatings and environmental protection.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Huizhen Sun,Xiuhua Chen,Shaoyuan Li,Wenhui Ma,Xiumin Chen,Dandan Wu,Kaixin Fu,Mingjun Xiao,Ming Wen
Developing efficient and selective recovery of Pd(II) adsorbents is crucial for addressing environmental pollution issues. Among them, covalent organic framework (COF) and metal organic framework (MOF) composites due to the multi-site functional groups are expected to exhibit excellent Pd(II) adsorption. However, the design and preparation of COF and MOF composite adsorbents for highly efficient adsorption of heavy metal Pd(II) still face many challenges. Herein, we constructed a series of novel core–shell structure UiO-66-NH 2 @TAP-COF (denoted as M@C) adsorbents (M@C-X, X = 1–5, representing different MOF doses) by Schiff base reaction and applied in the adsorption of Pd(II). The findings indicated that the M@C-3 exhibited ultra-high adsorption performance, reaching a capacity of 2134.1 mg/g, and displayed excellent selectivity, making it the best among similar materials. Experimental data and density functional theory (DFT) calculations revealed that the efficient and selective adsorption of Pd(II) is attributed to coordination interaction and strong electrostatic between Pd(II) and the abundant N and O groups in M@C. This work demonstrates the significant potential of the constructed core–shell M@C composites for the efficient and selective recovery of precious metal Pd(II).
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CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Longyun Zhang,Ganghua Zhou,Gaoran Chen,Heming Wang,Qian Zhao,Weiqin Yin,Jianjian Yi,Xingwang Zhu,Xiaozhi Wang,Xin Ning
The metal–organic frameworks (MOFs) rich in porous structures and their derivatives have been widely developed and applied to heavy metal adsorption. However, little attention has been paid to the subsequent treatment and reutilization of spent MOFs adsorbents. A potential feasible strategy is to develop MOFs-derived bimetallic catalysts for energy conversion. Herein, a bimetallic Ni-Cu 2 O-Cu/C nanocomposite (Ni-Cu/C) derived from spent Cu-based MOFs (CuBTC) adsorbents was fabricated and applied to improve the performance of photocatalytic CO 2 reduction. The results demonstrate that Ni doping could improve the charge transfer dynamics. The synthesized Ni-Cu/C catalyst exhibits a high CO yield (12.45 μmol g −1 h −1 ) in the pure water system in the absence of other photosensitizers and sacrificial agents, which is 2.05 folds higher compared to Cu/C. The CO 2 conversion selectivity of the synthesized Ni-Cu/C catalyst reaches up to 99.0%. The mechanism of photocatalytic CO 2 reduction reaction was further investigated by in-situ experiments and density functional theory calculation. The in-situ FT-IR characterization show that photogenerated electrons could effectively adsorb CO 2 to produce CO 2 − and optimize *CO immediate. This work not only emphasizes the unique design of bimetallic catalyst derived from spent MOFs adsorbent, but also contributes a feasible solution to its reutilization for enhanced CO 2 conversion.
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SOLAR ENERGY MATERIALS AND SOLAR CELLS
·
2024
·
IF 6.3
Le Huy Thai,Le Thi Thanh Nhi,Nguyen Minh Hiep,Dinh Thanh Khan,Trinh Ngoc Dat,Le Vu Truong Son,Truong Quang Trung,Le Hoang Sinh
A novel all-in-one electrochromic device from viologen-based Cu-MOF was demonstrated successfully for the first time. The viologen-based Cu-MOF was dispersed in a photochemical eutectic solvent and directly used as an electrochromic material with the outstanding advantage of good modulation ability in a wide range of visible light. The electrochromic device's (ECD) color changed from transparent and light lime green to blue during the change of potential from 0 V to −3.5 V. The bistability of the ECD was demonstrated by the transmittance degradation of less than 10 % over 1.79 h when the power was turned off. This showed that the ECD could maintain its optical state long without a continuous power supply.
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Journal of Saudi Chemical Society
·
2024
·
IF 5.8
Zhengjie Li,Miao Liu,Chunxia Fang,Huanshu Zhang,Tianyi Liu,Yixian Liu,Heli Tian,Jilong Han,Zhikun Zhang
The widespread use and subsequent accumulation of florfenicol (FFC), a common antibiotic, through the food chain poses significant risks to aquatic ecosystems and human health, necessitating effective strategies for its removal from water bodies. To solve the challenge, herein, we developed a novel aluminum-based metal–organic framework CAU-1, engineered for the efficient adsorption of FFC. CAU-1 contains the plentiful –NH 2 and μ-OH groups with the positively charged on the surface. In the adsorption process, CAU-1 perform hydrogen bonding interactions with FFC’s functional groups (−F, –OH, −Cl, –NH–, and −SO 2 –). Furthermore, the positively charged surface of CAU-1 enhances FFC adsorption via electrostatic attraction together. FFC adsorption equilibrium on CAU-1 is attained within 180 min with a monolayer adsorption capacity of 386 mg/g at 303 K, surpassing most of the reported adsorbents. The exothermic FFC adsorption process on CAU-1 remains largely unaffected by coexisting ions. Additionally, CAU-1 can be efficiently regenerated using a mixed solution of 0.1 M HCl and ethanol–water as an eluent. This work highlights CAU-1’s potential as an effective adsorbent for FFC removal, emphasizing the importance of tuning or designing surface functional groups on adsorbents to boost their adsorption capabilities.
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JOURNAL OF ALLOYS AND COMPOUNDS
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2025
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IF 6.3
Weijun Gui,Mingzhe Du,Xianmin Zhang,Miroslav Almáši,Lijia Wan,Lu Gan,Zhenxi Wang,Suhang Wu
The limited luminescence efficiency and poor stability of lanthanide-based metal-organic frameworks (Ln-MOFs) are the key factors restricting their practical applications. It is well known that high-temperature annealing can significantly enhance the photoelectric properties of inorganic materials, but it seems unfeasible for Ln-MOFs due to the existence of organic components. To overcome this dilemma, MOF-76 was synthesized by hydrothermal method and then hydrothermally annealed at 140 °C for 4 h. As a result, the annealing not only significantly improves the crystallinity of MOFs but also promotes their transition from the original tetragonal phase to the monoclinic phase. The annealed MOFs ( a MOF) exhibit about 3-fold emission enhancement and show better stability, especially under alkaline conditions or in water or saturated alkanes, such as cyclohexane, and dichloromethane. The total emission intensity of the as-prepared (AP) MOF is reduced to less than 1/10 compared to the a MOF due to the influence of water molecules. When the material was immersed in a mixture of ammonia and water, the a MOF emission remained stable, while the AP MOF emission rapidly decreased to approximately 12 % with an increasing volume ratio. Additionally, a notably enhanced 5 D 0 → 7 F 1 transition of Eu 3+ ions in MOF-76 has been observed for the first time. It was found that after hydrothermal annealing, the photoluminescence quantum yield of the MOF increases from 10.86 % to 61.48 %, and its synthesis yield can reach 73.8 %. The properties described above remarkably enhance the application values of the a MOFs. Interestingly, MOFs can also be solvothermal annealed, thus the schemes presented in this context open up novel approaches to significantly improve/modify the performance of other MOF materials. Finally, the obtained green and red emitting a MOFs combined with the N-CDs@starch were applied to warm white LED with the colour coordinates (CIE) of (0.3662, 0.3544), colour rendering index (CRI) of 88.5 and correlated colour temperature (CCT) of 4261 K.
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IONICS
·
2025
·
IF 2.6
Du Jia,Chen Lixuan,Wu Yiming,Wei Xin,Jia Jingyuan,Sun Kenan,Li Bingke
Nowadays, the advancement of eco-friendly, clean, sustainable and renewable new energy has emerged as a research priority for scientists worldwide. Electrolytic water technology is founded on the principle of electrochemical or photoelectric decomposition of water, is deemed as one of the most promising and most feasible approaches to reach industrial production. Traditional OER (oxygen evolution reaction) electrocatalysts like IrO 2 and RuO 2 are beset by high costs and vulnerability to poisoning. Hence, it is essential to develop more economical, more stable and more efficient materials for the application of OER reactions. In this study, a series of AQ-doped (AQ = anthraquinone) MOF-74 materials were fabricated through a one-step solvothermal approach. The surface loading of the conjugated organic small molecule AQ on CoNi-MOF-74 is capable of effectively boosting the inadequate electrical conductivity of the bulk MOF material, thus significantly enhancing the performance of OER. The optimized ratio of material composition of AQ20@MOF-74 displayed significantly enhanced OER activity. with a lower overpotential of 272 mV at 10 mA cm −2 and a smaller Tafel slope of 78 mV dec −1 . The research findings presented in this thesis provide a novel approach for the design and optimization of highly efficient OER electrocatalysts based on MOFs.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Yanxin Gao,Ting Cheng,Fankang Zhao,Guocheng Huang,Jinhong Bi
The treatment of emerging contaminants is essential but challenging. Herein, a novel MOF/PAN fibrous composite (TCPP@UiO-66/PAN) was synthesized and used as a self-cleaning membrane for the efficient removal of a typical emerging contaminant, diclofenac sodium (DF). The introduction of the secondary linker tetra(4-carboxyphenyl)porphyrin (TCPP) served to expand the pores and enhance its photocatalytic activity. TCPP@UiO-66/PAN shows higher adsorption capacity and initial adsorption rate than UiO-66/PAN. The maximum adsorption capacity of DF on TCPP@UiO-66/PAN reached 202 mg/g by Langmuir model. The DF adsorption mechanism involves the π-π/anion-π interaction, Lewis acid-base interaction, and hydrogen bonding. Based on the dynamic filtration experiment, TCPP@UiO-66/PAN exhibited a remarkable treatment capacity for DF-contaminated water, measuring 3.75 × 10 4 kg/kg. Given its fibrous membrane structure, TCPP@UiO-66/PAN could be easily separated from water and reused. In-situ photo-regeneration emerged as a highly effective method for regenerating TCPP@UiO-66/PAN after reaching adsorption saturation, with over 95 % DF degradation achieved under sunlight irradiation. The decomposition of DF primarily resulted from the generation of h + and 1 O 2 . Additionally, TCPP@UiO-66/PAN exhibited notable antibacterial properties when exposed to visible light. In vitro cytotoxicity assessments further confirmed the safety of these MOF/PAN composites. Combining the advantages of hybrid-linker strategy and fibrous composite, this work provided new insight into constructing MOF-based functional material for wastewater purification.
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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
·
2024
·
IF 4.1
Ting Lu,Xinyan Xiao,Fei Wang,Xia Cheng,Yu Zhang
A novel BiOBr/Ni-MOF composite was fabricated by in-situ growth of BiOBr nanosheets on Ni-MOF through a convenient precipitation process. The optimal photocatalytic performance was achieved with a Ni-MOF mass content of 45 wt% in the BiOBr/Ni-MOF composite. This composite exhibited remarkable efficiency, degrading 98.33 % of Rhodamine B in 90 min, surpassing the degradation rate constants of pristine BiOBr and Ni-MOF by 4.2 and 160 times, respectively. The superior performance was primarily ascribed to the efficient separation of photogenerated carriers facilitated by the formation of heterojunctions. Additionally, the increased specific surface area and pore structure provided numerous adsorption and active sites. Radical scavenger experiments and electron spin resonance experiments further revealed that O 2 − and h + played crucial roles in the degradation process. Furthermore, the structural properties of the prepared photocatalysts and the effects of different photocatalytic conditions on the degradation of RhB were investigated. This work offers an alternative perspective on the design and fabrication of BiOBr-based composite photocatalysts.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2024
·
IF 7.7
Yunqi Kuang,Ziwen Zhang,Kai Zhu,Yangang Sun,Kaiyang Wang,Chunping Yuan,Jie Lu,Yu Luo,Xijian Liu,Jian Wan
The glioma is one of the most aggressive tumors in humans, which is difficult to eradicate clinically. Therefore, we devised a porphyrin-based metal-organic frameworks (MOFs) crosslinking hyaluronic acid (HA) hydrogel nanocomposite through double-network (Cu-MOF-S-S-HA-Gel, CSSH-Gel), which is tumor responsive for enhanced gas therapy and sonodynamic therapy (SDT). Firstly, the hydrogels show extraordinary injectability and biocompatibility, which enables intratumor administration to circumvent the danger associated with surgery. The Cu-MOF-Cys and HA-Cys are interconnected through ether and disulfide bonds to establish a dual-network gel structure. The overexpressed glutathione (GSH) in tumor microenvironment (TME) reacts with disulfide bonds to release of the nanosensitizer (Cu-MOF). Subsequently, Cu-MOF generates reactive oxygen species (ROS) upon ultrasound irradiation for SDT, and releases L-cysteine(L-Cys) catalyzed by 3-mercapto pyruvate sulfotransferase (3-MST) to generate H 2 S for gas therapy. The CSSH-Gel obtained excellent synergistic anti-tumor effects (82.34 % inhibition ratio in vivo), which holds tremendous promise for the advancement of minimally invasive glioma therapies.
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JOURNAL OF HAZARDOUS MATERIALS
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2024
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IF 12.2
Xuanting He,Jihan Lu,Jiaxiang Liu,Zixuan Wu,Boyu Li,Zhong Chen,Wenquan Tao,Zhuo Li
Effectively addressing crude oil spills remains a global challenge due to its high viscosity and limited flow characteristics. In this study, we successfully prepared a modified sponge (PCP@MS) by embedding the photothermal material of Co-HHTP and coating the melamine sponge (MS) with low-surface-energy polydimethylsiloxane (PDMS). The PCP@MS exhibited outstanding hydrophobicity with WCA of 160.2° and high oil absorption capacity of 59–107 g/g. The PCP@MS showed high separation efficiency of 99.2% for various oil-water mixtures, along with notable self-cleaning properties and mechanical stability. The internal micro-nano hierarchical structure on the sponge surface significantly enhanced light absorption, synergizing with the photo-thermal conversion properties of Co-HHTP, enabled PCP@MS to achieve a surface temperature of 109.2 °C under 1.0 solar light within 300 s. With the aid of solar radiation, PCP@MS is able to heat up quickly and successfully lowering the viscosity of the surrounding crude oil, resulting in an oil recovery rate of 8.76 g/min. Density functional theory (DFT) calculation results revealed that Co-HHTP featured a zero-gap band structure, rendering advantageous electronic properties for full-wavelength light absorption. This in situ solar-heated absorbent design is poised to advance the practical application of viscous oil spill cleanup and recovery.
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