JOURNAL OF MATERIALS SCIENCE
·
2024
·Vol. 59
·期 44
·20624-20639
·
IF 3.5
She Houde,Chen Dongxu,Huang Jingwei,Wang Lei,Chen Jiufu,Chen Xiaoping,Wang Qizhao
The removal of volatile organic compounds has been a long-standing challenge, and NH 2 -MIL125, with its large specific surface area, has shown great promise in this regard. However, its limited number of active sites hinders its widespread application. To address this limitation, we report the successful synthesis of a series of Co 3 O 4 -modified NH 2 -MIL125 metal–organic framework (MOF) composites with a lamellar structure. Notably, the optimized 35% Co 3 O 4 /NH 2 -MIL125 composite exhibited exceptional performance, achieving 85.59% degradation and 76.58% CO 2 conversion under simulated sunlight. Moreover, this composite demonstrated excellent stability, maintaining a degradation rate of 79.67% over 520 min. The enhanced performance is attributed to the large specific surface area of NH 2 -MIL125, as well as the Co 3 O 4 modification, which provides new active sites, enhances light utilization efficiency, accelerates the separation of photogenerated carriers, and facilitates the generation of reactive radicals. This in-situ growth strategy for modifying NH 2 -MIL125 with Co 3 O 4 offers a novel approach to expand the application scope of NH 2 -MIL125 and enhance its performance in toluene degradation. Graphical abstract
Characterization of layered Co 3 O 4 -modified NH 2 -MIL125 catalysts, evaluation of photocatalytic degradation performance of toluene, photogenerated carrier migration, and separation studies.
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MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING
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2024
·
IF 4.2
Z.H.A.O.-X.U.A.N. Jiang
In this investigation, UiO-66-NH 2 was effectively synthesized through a solvothermal approach, utilizing benzoic acid and hydrochloric acid (HCl) as modulating agents. This synthesis process intentionally introduced defects mediated by benzoic acid, and the degree of these defects was precisely adjusted by the concentration of HCl. Subsequently, the material underwent a covalent modification process through an amidation reaction, resulting in the attachment of tetrakis (4-carboxyphenyl) porphyrin (TCPP). The results demonstrated a significant improvement in the photocatalytic reduction of Cr(VI), showcasing a 125 % elevation in reduction efficiency as compared to the unmodified UiO-66-NH 2 material serving as the baseline. The performance enhancement is due to the synergistic effect of the defect structure and TCPP modification, which enhances the light absorption, promotes charge transfer and separation, reduces the recombination rate, and improves the adsorption capacity and light absorption efficiency of Cr(VI). This research introduces an innovative approach and a highly effective catalyst, offering a novel solution for modifying metal-organic frameworks (MOFs) and enhancing their photocatalytic performance in the reduction of Cr(VI).
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Xiaoxia Ye,Zhihong Zheng,Jinwei Zhu,Jie Chen,Jianfei Zhou,Bi Shi
Adsorptive removal of mercury ion from wastewater has become a hot topic due to the toxicity and persistence; acquiring adsorbent materials with high-capacity, rapid-kinetic, super-selective while low-cost features are highly demanded. Herein, based on the full functionality of collagen fiber (CF) from the leather waste, we proposed an innovative synthetic approach through exploiting amino-functionalized ZIF-7 (ZIF-7-NH 2 ) as functional groups to facilely in-situ incorporate with CF, affording low-cost but effective adsorbent materials of CF/ZIF-7-NH 2 composite maximizing both functions of CF and ZIF-7-NH 2 in the Hg(II) capture. Remarkably, it exhibits an ultra-high capacity as high as 909.09 mg g - 1 , fast kinetics that could remove 99.01 % of 200 mg·L -1 within 20 min, and significant selectivity of S Hg/M ( K d Hg / K d M ) as large as 522–1017 over Mg 2+ , K + , Ca 2+ , Cd 2+ , and Mn 2+ . We understand such an impressive adsorption is contributed by the synergistic action between functional groups including on the CF and ZIF-7-NH 2 . This study offers an effective method for removing heavy metal ions, achieving efficient removal of Hg(II) ions for pollution control, and promoting the reuse of waste CF to reduce waste accumulation in various aspects.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2025
·
IF 9
Mazhar Khan,Zeeshan Akmal,Muhammad Mubashir Khan,Muhammad Tayyab,Seemal Mansoor,Muhammad Adnan Zeb,Amir Zeeshan,Ziwei Ye,Jinlong Zhang,Shiqun Wu,Lingzhi Wang
Metal-organic framework (MOF) based heterojunctions offer a promising strategy for CO 2 photoreduction, contributing to carbon neutrality and environmental remediation. However, the precise design and control of these heterostructures remain critical challenges. Herein, we report the precise construction of a heterostructure by integrating 2D ZnIn 2 S 4 nanosheets with NH 2 -MIL-125(Ti) for efficient CO 2 photoreduction in a sacrificial agent-free environment. A comprehensive investigation demonstrates robust interfacial interactions and work function differences between NH 2 -MIL-125(Ti) and ZnIn 2 S 4 , facilitating the formation of an interfacial electric field and enabling the construction of an S-scheme heterojunction. The directional migration of photogenerated charge carriers effectively suppresses their recombination, retaining the strong oxidative and reductive potential of the heterostructure components. In-situ infrared spectroscopy provides concrete evidence that the S-scheme heterojunction significantly enhances the formation of key intermediates, which are crucial for CO generation. The optimized NMT-5@ZIS achieves a CO yield of 17.30 umol g -1 h −1 without sacrificial agents, representing 8.6 and 6.6-fold improvements over pristine NH 2 -MIL-125(Ti) and ZnIn 2 S 4 , respectively. This work bestows an innovative insight into the construction of MOF-based S-scheme heterojunctions, opening new avenues for practical applications in energy storage and photocatalysis.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Yuchen Cui,Xiaolei Cui,Lubomira Tosheva,Chunzheng Wang,Yongming Chai,Zixi Kang,Qiang Gao,Kun Wang,Zhihan Zhang,Hailing Guo,Daohong Xia,Daofeng Sun
Effective separation of CO 2 from CH 4 is crucial for the purification of natural gas, which requires membrane materials with high permeability, selectivity, and stability of under high pressures. In this work, a high CO 2 -affinity MOF-based nanofiller (P in @NH 2 -UiO-66) was prepared and integrated in polyetherimide (PEI) to prepare mixed matrix membranes (MMMs) for enhanced CO 2 /CH 4 separation capabilities. The P in @NH 2 -UiO-66 nanofiller comprised an in situ-formed polyethyleneimine-NH 2 -UiO-66 composite prepared via a one-pot synthesis. The polyethyleneimine was covalently attached to the H 2 BDC-NH 2 ligand allowing for a stronger integration within the PEI matrix. The polyethyleneimine affects the nucleation of MOF, leading to miniaturization of the MOF particles. The smaller-sized filler is beneficial for improved interaction at the filler-matrix interface. The numerous amino functionalities grafted onto the NH 2 -UiO-66 increased the CO 2 adsorption sites, thereby enhancing the affinity for CO 2 . Owing to the improved interaction, the elevated CO 2 attraction, and the inherent properties of the porous NH 2 -UiO-66, the fabricated MMMs preformed superior in separating CO 2 /CH 4 . The 30-P in @NH 2 -UiO-66-PEI membrane (containing 30 wt% nanofiller) exhibited a CO 2 /CH 4 selectivity of 27.7 and a CO 2 permeability of 2498.9 Barrer. The CO 2 permeability was 21 times greater than that of the pristine PEI membrane, and 4 times higher compared to P@NH 2 -UiO-66 MMM with polyethyleneimine modified MOF filler prepared by a traditional wet impregnation method. Additionally, the novel MMM demonstrates excellent separation stability under conditions that mimic industrial settings, demonstrating its potential application for natural gas purification.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Yingqi Xia,Lijia Liu,Yudan Wang,Chunhong Zhang,Yawen Liu
CH 3 Hg + in water is a neurotoxin that is difficult to eliminate and is readily absorbed by the human body through food chains. In this study, thioctic acid was grafted onto the surface of NH 2 -MIL-101 via an amidation reaction to prepare an adsorption material for the rapid and effective removal of CH 3 Hg + , which is designated as LA-MIL-101.The synthesis of LA-MIL-101 was confirmed through analyses including FT-IR, XRD, SEM, TGA, and XPS. BET results indicate that the specific surface area of LA-MIL-101 is 464.92 m 2 ·g −1 . The ideal conditions for CH 3 Hg + adsorption were explored by varying environmental factors such as pH, contact time, and temperature. Furthermore, the introduction of sulfur significantly enhanced the adsorption capacity for CH 3 Hg + . Batch adsorption experiments demonstrate that LA-MIL-101 exhibits an exceptionally rapid adsorption rate, achieving over 88.3 % of the total removal rate within just one minute. Additionally, LA-MIL-101 shows remarkable adsorption efficacy across a broad pH range. The adsorption behavior of LA-MIL-101 for CH 3 Hg + aligns with the Elovich and Langmuir models, with a maximum adsorption capacity reaching 1391.77 μg·g −1 . LA-MIL-101 also displays a strong anti-interference capability in environments containing humic acid or Na + . Notably, it maintains high removal efficiency under conditions involving coexisting cations, as well as in simulated surface water, simulated groundwater, and natural seawater. Moreover, LA-MIL-101 demonstrates good stability and recyclability, retaining effective adsorption after five adsorption/desorption cycles. XPS results elucidate the adsorption mechanism of CH 3 Hg + , highlighting interactions with sulfur (S) and nitrogen (N) atoms. Overall, LA-MIL-101 exhibits high practicality and significant potential for application in the emergency treatment of CH 3 Hg + in aquatic environments.
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MICROCHEMICAL JOURNAL
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2025
·
IF 5.1
Tong Zhang,Xiaojing Liang,Lijing Chang,Xiaobing Lu,Shuning Li,Shuai Wang,Licheng Wang
For high-performance liquid chromatography (HPLC) laboratories, expanding the scope of application of a column to the extent that it can substitute for two or even three single-mode columns are crucial for reducing laboratory operational costs. The mixed-mode stationary phase, which exhibits properties suitable for various applications, can to a certain degree meet this demand. Because the separation mode of mixed-mode stationary phase (which possessed multiple interaction sites) can be modulated by adjusting mobile phase condition. Consequently, the analysis and separation of hydrophilic and hydrophobic samples can be accomplished within a same column. In this research, we developed a novel stationary phase by functionalizing silica with NH 2 -carbon dot and hydrogel, which can be utilized in mixed-mode liquid chromatography. The successful fabrication of this stationary phase was validated through the application of Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), and Thermogravimetric Analysis (TGA), among other techniques. Additionally, the evaluation of chromatographic performance revealed that this stationary phase can be effectively utilized in both hydrophilic interaction chromatography (HILIC) and reversed-phase liquid chromatography (RPLC) modes. The column demonstrated superior separation performance, including an improved peak shape and enhanced separation selectivity, in comparison to commercial NH 2 -column and Diol-column under HILIC mode. This was particularly evident when analyzing a range of polar analytes, including saccharides, nucleosides/bases and alkaloids in HILIC mode. In short, a novel mixed-mode stationary phase was successfully developed by integrating NH 2 -CD with hydrogel, thereby broadening the potential applications of hydrogels in HPLC. In addition, this stationary phase presents significant potential for the analysis of hydrophilic, hydrophobic, and complex samples. This allows a single column to serve multiple purposes, thereby reducing the operational costs of laboratories.
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Particuology
·
2024
·
IF 4.1
Jingchuan Wang,Junhong Luo,Yong Yao,Jiangfeng Song,Yan Shi
To improve room-temperature hydrogen storage, palladium (Pd) nanoparticles were innovatively decorated by carbon bridge onto the amino-group functioned Zr-terephthalate metal-organic framework (MOF) UiO-66 to reduce the diffusion energy barrier and then improve the hydrogen spillover effect. Powder X-ray diffraction shows broad Pd peak and retained UiO-66-NH 2 integrity after Pd decoration. The hydrogen uptake capacity show that UiO-66-NH 2 -Pd exhibits best hydrogen storage performance than UiO-66-NH 2 and pristine UiO-66. The hydrogen up taken in Pd decorated UiO-66 (UiO-66-NH 2 -1Pd) was close to 4 wt% under 20 MPa at room temperature. Density functional theory (DFT) calculations show that hydrogen adsorption energy of UiO-66-NH 2 -Pd was −0.5897 eV, which was much lower than that of UiO-66-NH 2 (−0.3716 eV) and UiO-66 (−0.2975 eV). Ultimately, Pd decorated NH 2 group functioned UiO-66 enable improve storage capacities through hydrogen spillover under ambient conditions which could satisfy the demand for sustainable energy, especially for the long-term storage energy media.
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JOURNAL OF APPLIED POLYMER SCIENCE
·
2024
·
IF 2.7
Wei Zhao,Hongjing Liu,Chengpeng Zhang,Yuyang Cao,Yuying Xu,Xueli Liu,Zhen Lu
Metal–organic frame UiO-66-NH 2 was modified by 3-glycidyl ether oxypropyl trimethoxysilane (KH560), and KH560-UiO-66-NH 2 was synthetized and added to Pebax to prepare KH560-UiO-66-NH 2 /Pebax mixed matrix membranes (MMMs). The epoxy group of KH560 had an amine-epoxidation reaction with the NH 2 in UiO-66-NH 2 , which prevented UiO-66-NH 2 from agglutinating in the MMMs. In addition, the N H bond and OH bond of KH560-UiO-66-NH 2 could theoretically form hydrogen bonds with CO and N H bonds in the main chain of polymerization, respectively, so as to improve the interfacial compatibility between fillers and polymers. The structure and properties of the filler particles and MMMs were evaluated by Fourier transform infrared spectrometer, x-ray diffraction, scanning electron microscopy, and thermogravimetric analyzer. The results showed that the filler particles were successfully synthesized, and had good crystallinity, uniform size distribution, and good thermal stability. The inorganic and organic interfaces of MMMs had no obvious interface defects. The obtained KH560-UiO-66-NH 2 /Pebax MMMs showed CO 2 permeability of 111.52 Barre and CO 2 /N 2 selectivity of 92.16, which were 85.65% and 88.73% higher than that of pristine membranes, respectively. The gas separation performance of MMMs was significantly improved, exceeding the upper bound of 2008 Robeson.
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Energy Technology
·
2025
·
IF 3.6
Ming Yan,Haoyu Chen,Yu Zhu,Yuxiao Deng,Zhuanlong Yan,Ziyi Lu,Yanlin Chen
In this study, NH 2 –SiO 2 @Ti 3 C 2 T x core–shell microspheres with different Ti 3 C 2 T x contents are prepared by coating Ti 3 C 2 T x nanosheets on the surfaces of SiO 2 microspheres using an electrostatic self-assembly method. The structures, elemental compositions, and microscopic morphologies of NH 2 –SiO 2 @Ti 3 C 2 T x microspheres are investigated by X-Ray diffraction, Fourier-transform infrared spectroscopy, field-emission scanning electron microscopy, and X-Ray photoelectron spectroscopy. The results show that Ti 3 C 2 T x nanosheets are uniformly coated on the surfaces of the SiO 2 microspheres, and the surfaces of the SiO 2 microspheres are modified by NH 2 . The maximum specific surface area of NH 2 –SiO 2 @Ti 3 C 2 T x composite doped with 15 wt% Ti 3 C 2 T x is 29.937 m 2 g −1 , with an average pore size of 0.11848 cm 3 g −1 . The electrochemical performance test results show that after 100 cycles at a C rate of 0.2C, the specific capacity of the NH 2 –SiO 2 @Ti 3 C 2 T x anode material increases by 270.1% compared to that of SiO 2 , reaching 142.5 mAh g −1 . Compared with SiO 2 , the NH 2 –SiO 2 @Ti 3 C 2 T x materials have higher electrical conductivities and Li ion diffusion rates, thereby improving their rate performances, and the discharge specific capacities and cycling stability are superior to those of the SiO 2 anode material.
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STAR Protocols
·
2023
·
IF 0
Shuchao Jiang,Jikai Sun,Guoqing Ren,Weiqiao Deng
Summary CO 2 capture and utilization into liquid fuels and high-added-value chemicals has been regarded as an attractive strategy to mitigate excessive carbon emissions. Here, we present a protocol to capture and convert CO 2 into pure formic acid (HCOOH) solution and solid fertilizer (NH 4 H 2 PO 4 ). We describe steps for synthesis of an IRMOF3-derived carbon-supported PdAu heterogeneous catalyst (PdAu/CN-NH 2 ), which can efficiently catalyze (NH 4 ) 2 CO 3 -captured CO 2 into formate under ambient conditions. For complete details on the use and execution of this protocol, please refer to Jiang et al. (2023). 1
研究领域:
环境科学
·
化学工程
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PubMed
MICROCHIMICA ACTA
·
2019
·Vol. 186
·期 11
·1-8
·
IF 5.479
Guo Lan,Liu Yuan,Qu Fengli,Liu Zhe,Kong Rongmei,Chen Guang,Fan Wenjing,Xia Lian
A luminescent metal organic framework (LMOF) of type UiO-66-NH 2 was chosen for specific and sensitive detection of trace levels of hypochlorite. Hypochlorite causes the quenching of the blue fluorescence of nano-UiO-66-NH 2 (with excitation/emission maxima at 325/430 nm), and this finding forms the basis for a fluorometric assay for hypochlorite. The method overcomes disadvantages of conventional redox-probes which are interfered by oxidants with oxidation capability stronger than that of hypochlorite. Compared with other fluorescent probes for sensing hypochlorite, UiO-66-NH 2 has a comparable detection limit of 0.3 μmol L −1 and a broad linearity relationship in the range of 1–8 μmol L −1 . The probe was successfully applied to the detection of hypochlorite in complex water samples and living Hela cells.
Schematic representation of hypochlorite induced quenching of the blue fluorescence of nano-UiO-66-NH 2 (with excitation/emission maxima at 325/430 nm) through energy transfer. It overcomes disadvantages of conventional redox-probes which are interfered by oxidants with oxidation capability stronger than that of hypochlorite.
研究领域:
分析化学
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材料科学
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生物医学
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