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MOF-74(Ni)
MICROPOROUS AND MESOPOROUS MATERIALS · 2017 · IF 3.615

One-step synthesis of magnetic and porous Ni@MOF-74(Ni) composite

Tingting Xu,Xudong Hou,Shengjun Liu,Bo Liu

We demonstrated a facile and efficient method for the preparation of a magnetic and porous Ni@MOF-74(Ni) [Ni 2 (DOBDC), DOBDC = 2, 5-dihydroxyterephthalate] composite by one-step solvothermal reaction of Raney Ni and DOBDC. Ni in the reaction not only acted as the core of the composite, but also provided metal source for the formation of MOF-74(Ni). The Ni@MOF-74(Ni) composite exhibits both magnetic characteristics and high porosity, enabling it an efficient candidate for dye removal and target drug delivery system. The adsorption amount of rhodamine b reached up to 177.8 mg g −1 , and 4.1 mg g −1 for ibuprofen.

CAS / MDL: 7440-02-0 81-88-9
研究领域: 材料科学 · 化学工程 · 环境科学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2021 · IF 8.128

Taming structure and modulating carbon dioxide (CO2) adsorption isosteric heat of nickel-based metal organic framework (MOF-74(Ni)) for remarkable CO2 capture

Lei Lei,Yan Cheng,Changwei Chen,Mohammadreza Kosari,Zeyu Jiang,Chi He

Though the highest CO 2 capture capacity belongs to liquid amine-solutions, solid matters capable of CO 2 capture are also highly sought, providing that, they offer at least analogous CO 2 adsorption capacity and CO 2 /N 2 selectivity. Herein, a surprisingly high-performance Ni-based metal–organic framework for CO 2 adsorption, namely MOF-74(Ni), was synthesized by a facile condensation reflux approach. It was found that the structure and CO 2 adsorption isosteric heat of MOF-74(Ni) could tune upon varying the synthesis duration under various temperatures. The optimized MOF-74(Ni)-24-140 (synthesized at 140 °C for 24 h) displays outstanding CO 2 adsorption capacity of 8.29/6.61 mmol/g at 273/298 K under normal pressure of 1.0 bar, several times higher than previously reported MOF-74-Ni (2.0/2.1 times), UTSA-16 (1.5/1.6 times), and DA-CMP-1 (3.6/4.9 times) under similar conditions. The excellent CO 2 capture capacity is associated to the abundant adsorption sites (mainly arising from the cationic Ni 2+ ions) and narrow micropore channels (mainly arising from the cage structure of Ni 2+ ions coordinated with organic linkers). Offering a high CO 2 selectivity (CO 2 /N 2  = 49) and a well-tuned isosteric heat of CO 2 adsorption (27–52 kJ/mol) besides its decent CO 2 capture capacity, MOF-74(Ni) strongly stands out as an efficient and strong CO 2 capturing material with industrial scale applicability.

CAS / MDL: 64-17-5 68-12-2 610-92-4
研究领域: 材料科学 · 环境科学
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ANALYTICAL AND BIOANALYTICAL CHEMISTRY · 2020 ·Vol. 412 ·期 26 ·7227-7236 · IF 3.637

Synthesis of a molecularly imprinted polymer using MOF-74(Ni) as matrix for selective recognition of lysozyme

Li Jie,Ma Miaoxia,Zhang Chenhui,Lu Rui,Zhang Lingyi,Zhang Weibing

A molecularly imprinted polymer and metal organic framework were combined to prepare protein imprinted material. MOF-74(Ni) was used as a matrix to prepare surface-imprinted material with lysozyme as a template and polydopamine as an imprinting polymer. MOF-74(Ni) not only provides a large surface area (150.0 m 2 /g) to modify the polymer layer with more recognition sites ( Wt (Ni) = 42.24%), but also facilitates the immobilization of lysozyme by using the chelation between Ni 2+ of the MOF-74(Ni) and protein. The thin polydopamine layer (10 nm) of the molecularly imprinted material (named MOF@PDA-MIP) enables surface imprinting. Benefiting from the thin polymer layer, MOF@PDA-MIP reached adsorption equilibrium within 10 min. The maximum adsorption capacity reaches 313.5 mg/g with the highest imprinting factor (IF) of 7.8. The specific recognition sites can distinguish target lysozyme from other proteins such as egg albumin (OVA), bovine serum albumin (BSA) and ribonuclease A (RNase A). The material was successfully applied to separation of lysozyme from egg white. Graphical abstract

CAS / MDL: 64-19-7 67-56-1 100-21-0
研究领域: 材料科学 · 生物技术 · 分析化学
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SENSORS AND ACTUATORS B-CHEMICAL · 2022 · IF 9.221

Surface initiated encapsulation of MOF-74 (Ni) on magnetic prickly-like nickel rods combined with silver nanoparticle decoration for simultaneous and selective surface-enhanced Raman spectroscopy analysis of T-2 and deoxynivalenol

Kun Ge,Yuling Hu,Gongke Li

Herein, Ag nanoparticles decorated MOF-74 (Ni) encapsulated magnetic prickly-like nickel rods (NiRs@MOF-74 (Ni)/Ag) was firstly designed and fabricated for simultaneous surface-enhanced Raman spectroscopy (SERS) analysis of mycotoxins in food samples. The prickly-like NiRs not only provide magnetism with anisotropy structure, but also directly supply Ni 2+ for surface initiated encapsulation of MOF-74 (Ni) on NiRs. The as-fabricated NiRs@MOF-74 (Ni)/Ag exhibits good SERS activity due to the enrichment effect of magnetic NiRs, adsorption of MOF-74 (Ni) and localized surface plasmon resonance properties of AgNPs . The enhancement factor for 5,5′-dithiobis-(2-nitrobenzoic acid) and 4-mercaptobenzoic acid can reach 10 8 level with limits of detection (LOD) of 1.0 ng/L. Subsequently, the magnetic aptamer probes based on NiRs@MOF-74 (Ni)/Ag were fabricated for simultaneous, sensitive and selective SERS analysis of T-2 and deoxynivalenol in food samples. The method exhibited satisfactory linearity in range of 0.5–750.0 μg/L and 0.3–750.0 μg/L with LOD of 0.15 and 0.08 μg/L for T-2 and deoxynivalenol, respectively. The relative errors between the developed method and standard HPLC-MS ranged from −7.7 to 1.4%. Our results open a new venue in design and fabrication of magnetic SERS substrates with unique property for quantification of multiple mycotoxins in complex samples.

CAS / MDL: 7791-20-0 7761-88-8
研究领域: 食品科学 · 分析化学 · 材料科学
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INORGANIC CHEMISTRY · 2019 · IF 4.85

Microwave-Assisted Rapid Synthesis of Well-Shaped MOF-74 (Ni) for CO2 Efficient Capture

Changwei Chen,Xiangbo Feng,Qing Zhu,Rui Dong,Rui Yang,Yan Cheng,Chi He

In the present work, a series of MOF-74 (Ni) materials with narrow micropore channels and abundant unsaturated metal sites was respectively prepared via hydrothermal (HT), condensation reflux (CE), and microwave-assisted (MW) methods. The physicochemical properties of synthesized materials were characterized by powder X-ray diffraction, N2-sorption, field-emission scanning electron microscopy, Fourier-transform infrared (FTIR), thermogravimetric (TG)/TG-FTIR, X-ray photoelectron spectroscopy, UV–vis–near infrared, NH3/CO2-temperature programmed desorption, and in situ diffuse reflectance infrared Fourier transform spectroscopy. Their CO2/N2 adsorption performances were evaluated by isotherm adsorption and dynamic adsorption experiments. We found that the MW is a rapid and facile protocol for the synthesis of MOF-74 (Ni) materials with highly efficient CO2 capture capacity. The well-shaped MW-140 adsorbent with superior CO2 adsorption capacity of 5.22 mmol/g at 25 °C can be obtained within 60 min by the MW process, almost 6 times higher than that of the commercial activated carbon (0.89 mmol/g). Results of dynamic adsorption experiments showed that the MW-140 material possesses the highest CO2 adsorption capacity of 3.37 mmol/g under humid conditions (RH = 90%). Importantly, MW-140 has excellent adsorption stability and recyclability, superior CO2 capture selectivity (CO2/N2 = 31), and appropriate isosteric heat in CO2 adsorption (21–38 kJ/mol), making it a promising and potential material for industrial CO2 capture. Characterization results demonstrated that the high capture capability of MOF-74 (Ni) materials can be attributed to the synergistic effect of abundant narrow micropore channels and rich five-coordinated Ni2+ open metal sites which are beneficial for the trapping of CO2 molecules.

研究领域: 材料科学 · 环境化学 · 无机化学 · 碳捕集与封存 · 纳米材料
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2025 · IF 3.9

Hierarchically Porous Metal–Organic Framework Assembled by MOF-74-Ni Nanoparticles for Enhanced Photocatalytic CO2 Reduction

Xin-Ran Shi,Sai-Nan Guo,Ruoxi Zhang,Biao Yang,Hua Zou,Jie-Xin Wang

Metal–organic frameworks (MOFs) have emerged as pivotal materials for the photocatalytic reduction of CO2 to CO due to their exceptionally high surface areas and abundant active sites. However, most of the currently reported MOFs are confined to micropores (<2 nm), which limits adsorption/desorption and substance transport during photocatalytic CO2 reduction reactions. Herein, hierarchically porous MOFs (HP-MOF-74) were synthesized based on the assembly of MOF-74-Ni nanoparticles with different particle sizes (21, 42, and 85 nm) using spray-drying technology. The simultaneous enhancement of CO2 adsorption performance and photoelectroactivity was achieved in HP-MOF-74 due to the additional mesoporous structure formed by the nanoparticle stacking. The HP-MOF-74 exhibits 1.14–1.38 times improvement in the CO2 adsorption capacity compared to the corresponding initial MOF-74 nanoparticles (N-MOF-74). Meanwhile, the hierarchical architecture enhances photon utilization through improved light reflections and accelerates electronic transmission via additional mesopore pathways. These synergistic advantages collectively contribute to a 1.2–2.1 times enhancement in the CO generation rates of HP-MOF-74 compared with N-MOF-74 counterparts. Particularly, HP-MOF-74–42 nm demonstrated the highest CO production rate of 6.65 μmol h–1, outperforming most reported MOF-based photocatalysts. The construction of hierarchically porous MOFs provides a new idea for the design of highly efficient CO2 reduction photocatalysts.

研究领域: 材料科学 · 环境科学 · 化学工程 · 纳米技术
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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

Inducing nucleation of MOF-74(Ni) with sepiolite for construction of hierarchically porous composites to synergistically enhance CO2 adsorption and desorption performance

Chenguang Qian,Fang Yuan,Yi Wen,Hang Li,Jialin Liang,Yihan Xu,Xiaohan Li,Gaofeng Wang,Chunquan Li,Zhiming Sun

The synchronous enhancement of CO 2 adsorption capacity and desorption efficiency while reducing material costs, remains a major challenge in CO 2 capture technology. Metal–organic frameworks (MOFs) are frequently hindered by high synthesis costs, structural instability, and poor regenerability. Herein, MOF-74(Ni)@sepiolite (MOF-74(Ni)@SEP) composites with hierarchical pore structures are prepared via an in-situ hydrothermal method. Naturally abundant SEP serves as a morphology modulator, reducing energy barriers and facilitating crystal growth, thereby lowering synthesis costs. Additionally, SEP acts as a structural scaffold, anchoring onto the surface of MOF-74(Ni) to enhance thermal stability and construct a hierarchical pore network. Compared to pure MOF-74(Ni), the composite exhibits faster CO 2 diffusion and improved mass transfer, as confirmed by zero-length column (ZLC) analysis. Benefiting from these structural advantages, 2-MOF-74(Ni)@SEP-(100 °C,16 h) demonstrates excellent cycling stability, maintaining over 98 % of its CO 2 adsorption capacity after 10 cycles. Even under simulated flue gas conditions (338 K, humid and oxygen-containing), the composite maintains high CO 2 uptake, confirming its superior thermal and moisture tolerance. Mechanistic analysis reveals preferential coordination of CO 2 with Ni 2+ Lewis acid sites, while the hierarchical pore structure facilitates CO 2 desorption performance. This work provides a cost-effective and scalable pathway toward CO 2 capture under realistic industrial conditions.

研究领域: 材料科学 · 环境工程 · 碳捕集与封存 · 金属有机框架材料(MOFs) · 多孔材料
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