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UIO-66
JOURNAL OF CHROMATOGRAPHY A · 2014 · IF 4.258

Preparation and evaluation of silica-UIO-66 composite as liquid chromatographic stationary phase for fast and efficient separation

Zhiming Yan,Jiangnan Zheng,Jinfeng Chen,Ping Tong,Minghua Lu,Zian Lin,Lan Zhang

A silica-UIO-66 composite was fabricated by a simple hydrothermal method and then applied as liquid chromatographic stationary phase for fast and efficient separation. X-ray diffraction patterns showed the presence of UIO-66 crystals in the silica-UIO-66 composites; while scanning electron microscope (SEM) images revealed that silica-UIO-66 composites were a homogeneous mixture of silica bead and UIO-66 crystals. A variety of substituted aromatics, chlorobenzene compounds and polycyclic aromatic hydrocarbons (PAHs) were used to evaluate the retention properties of the silica-UIO-66 composite packed column. Under the optimized conditions, baseline separation of ethylbenzene (EB) and styrene was obtained with high resolution and short retention time. In addition, the silica-UIO-66 composite packed column also showed some advantages in separation of positional isomers, with which baseline separation of EB and xylene, chlorotoluene and dichlorobenzene isomers was achieved. Moreover, the retention mechanisms of these compounds were also discussed in detail. The relative standard deviations (RSDs) for the separation of EB and xylene, chlorotoluene and dichlorobenzene isomers, as well as EB and styrene were 0.42–0.9%, 1.0–1.9%, 0.75–2.0%, and 0.9–2.1% for the retention time, peak area, peak height, and half peak width, respectively. The column efficiencies for EB, p-chlorotoluene, p-dichlorobenzene and styrene were 8780, 9060, 9990 and 5130 plates/m. The successful applications suggested high potentials of silica-MOFs composite as stationary phase for fast and efficient liquid chromatography separation.

CAS / MDL: 10026-11-6 100-21-0
研究领域: 分析化学 · 材料科学
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APPLIED ORGANOMETALLIC CHEMISTRY · 2024 · IF 3.7

Dicationic ionic liquid-grafted UiO-66 as efficient catalyst for CO2 conversion into cyclocarbonate under cocatalyst-free and solventless conditions

Fangfang Li,Xiaofang Hou,Ying-Hua Zhou

CO 2 chemical fixation offers a feasible approach for carbon mitigation and high-value utilization, but it is still challenging to develop an efficient catalyst for CO 2 conversion into cyclic carbonate. Herein, the triethylenediamine-derived dicationic ionic liquids (DIL-X, X = Cl, Br, and I) were grafted into UiO-66 linkers through self-assembly of Zr 4+ ions and the mixed ligands of terephthalic acid and DIL-bearing dicarboxylic acid, resulting in UiO-66-DIL-X n , ( n designated as molar amount of the feeding DIL-X). Their catalytic performance was evaluated by the epoxide cycloaddition reaction in the absence of solvent and cocatalyst. Among them, the UiO-66-DIL-Cl 0.4 catalyst exhibited outstanding performance, with a chloropropene carbonate yield of 92% and a high selectivity of 99% under 0.1 MPa CO 2 at 110 °C for 16 h. Its high activity could be ascribed to the cooperativity among Lewis acidity of MOF nodes, the enhanced CO 2 absorption, and the strong nucleophilicity offered by halogen ions of ionic liquid-modified MOF. Moreover, UiO-66-DIL-Cl 0.4 presented excellent recyclability and substrate extension. A potential catalytic mechanism for the epoxide-CO 2 cycloaddition into cyclic carbonate has been proposed. This work will shed light on the rational design of functionalized MOFs-based catalysts for CO₂ utilization.

研究领域: 材料科学 · 催化化学
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JOURNAL OF MEMBRANE SCIENCE · 2019 · IF 7.015

Bimetallic Ce-UiO-66-NH2/diatomite (CUD) self-assembled membrane simultaneously with synergetic effect of phase equilibrium and rate separation

Jiaqi Wang,Yuqing Zhang,Ying Wang,Shuai Sun

To efficiently clean oily wastewater with the linear anion polyacrylamide (APAM), selective adsorption strategy belonging to phase equilibrium separation is introduced into the membrane separation . Herein, bimetallic Ce-UiO-66-NH 2 /diatomite (CUD) were first synthesized by a one-step hydrothermal method and then employed as a functional layer to form CUD self-assembled membrane (CSA-membrane). CUD particles were characterized by FT-IR, XRD and SEM, and CSA-membrane was observed by SEM. The separation and the selective adsorption properties of CSA-membrane formed under the optimum conditions for APAM in oily wastewater were investigated. The results demonstrate that the size of CUD particles with proper sphericity is mainly 20 μm. Furthermore, CSA-membrane simultaneously exhibits fascinating separation and selective adsorption properties for cleaning oily wastewater, namely the concentration of oil decreases from 78.1 mg L -1 to 6.8 mg L -1 , and flux of CSA-membrane reaches 789.5 L m -2  h -1 . Remarkably, the adsorption capacity of CSA-membrane for APAM is 161.5 mg g -1 , while showing the APAM removal rate of 51.3%. Therefore, CSA-membrane with the synergetic effect of phase equilibrium and rate separation is promising alternative for cleaning oily wastewater with APAM.

研究领域: 环境科学 · 材料科学
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Frontiers of Chemical Science and Engineering · 2022 ·Vol. 16 ·期 9 ·1387-1398 · IF 4.803

Integrating of metal-organic framework UiO-66-NH2 and cellulose nanofibers mat for high-performance adsorption of dye rose bengal

Han Yuyao,Xia Lei,Zhuang Xupin,Liang Yuxia

UiO-66-NH 2 is an efficient material for removing pollutants from wastewater due to its high specific surface area, high porosity and water stability. However, recycling them from wastewater is difficult. In this study, the cellulose nanofibers mat deacetylated from cellulose acetate nanofibers were used to combine with UiO-66-NH 2 by the method of in-situ growth to remove the toxic dye, rose bengal. Compared to previous work, the prepared composite could not only provide ease of separation of UiO-66-NH 2 from the water after adsorption but also demonstrate better adsorption capacity (683 mg·g −1 ( T = 25 °C, pH = 3)) than that of the simple UiO-66-NH 2 (309.6 mg·g −1 ( T = 25 °C, pH = 3)). Through the analysis of adsorption kinetics and isotherms, the adsorption for rose bengal is mainly suitable for the pseudo-second-order kinetic model and Freundlich model. Furthermore, the relevant research revealed that the main adsorption mechanism of the composite was electrostatic interaction, hydrogen bonding and π — π interaction. Overall, the approach depicts an efficient model for integrating metal-organic frameworks on cellulose nanofibers to improve metal-organic framework recovery performance with potentially broad applications.

研究领域: 材料科学 · 环境科学
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JOURNAL OF MOLECULAR LIQUIDS · 2024 · IF 5.3

Grafting of acidic ionic liquids onto the NH2-UiO-66 for butyric acid glyceride synthesis through heterogeneous catalysis of esterification

Jiawei Zheng,Xiaoyi Zhang,Zhuowa Li,Nanjing Zhong

Immobilization of acid ionic liquid (AIL) for heterogeneous catalysis is benificial for products separation and recycling the AIL for continuing reuse. In this study, AIL was grafted onto the amino group functionalized zirconium-based metal organic framework (NH 2 -UiO-66) to catalyze esterification for short chain fatty acid glycerides synthesis. AIL of 1-(4-Sulfobutyl)-3-Methylimidazolium Hydrogen Sulfate ([HSO 3 -BMIM][HSO 4 ]) was found suitable for short chain fatty acid glycerides after screening varied fatty acids with chain length from 4 to 18. [HSO 3 -BMIM][HSO 4 ] was therefore grafted and butyric acid glyceride was synthesized. Reaction conditions were optimized by means of single factor study and orthogonal experiment. The reusability of the AIL@NH 2 -UiO-66 was evaluated. The AIL@NH 2 -UiO-66 showed good esterificaiton performance and fine reusability. Butyric acid conversion (converted into the glycerides of mono-, di- and tributyrin) at 62.16% was obtained under the optimum conditions. In addition, the present AIL@NH 2 -UiO-66 was quite stable, and 67.39% of its initial esterification activity was retained after 11 cycles of reuse, suggesting it was potential in the esterification reaction.

研究领域: 化学工程 · 催化材料科学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2018 · IF 3.779

Effects of water environmental factors on the photocatalytic degradation of sulfamethoxazole by AgI/UiO-66 composite under visible light irradiation

Chao Wang,Yao Xue,Peifang Wang,Yanhui Ao

It is necessary to find visible light responsive photocatalysts for rapid and simple degradation of organic pollutants in water environment. In this work, a visible light responsive composite photocatalyst AgI/UiO-66 was prepared by an in situ growth method. Sulfamethoxazole (SMZ) antibiotic was selected as the target contaminant to probe the photocatalytic performance of the as-prepared AgI/UiO-66 composite under visible light irradiation. The results showed that the photocatalytic performance of the AgI/UiO-66 composite enhanced significantly compared to pure AgI. The effects of typical environment factors (i.e. pH, inorganic salt ions and common anions) on the degradation of SMZ were evaluated extensively. Results showed that the investigated pH (5.2, 7.0, 9.5) had no apparent effect on the photocatalytic degradation of SMZ except pH 2.5, at which the degradation rate of SMZ decreased significantly. In addition, inorganic salt ions and Cl − , HCO 3 − and SO 4 2− anions in water exhibited no apparent effect on the degradation of SMZ. The effect of water matrix on the degradation of SMZ was also investigated. In the river water, the removal efficiency of SMZ was reduced compared with the cleaner water matrix. The capture experiments of radicals confirmed that superoxide radicals ( O 2 − ) and hydroxyl radicals ( OH) were the main active species for the photocatalytic degradation of SMZ in the present work. Finally, the tentative degradation pathways of SMZ were proposed based on the intermediates analysis.

研究领域: 环境科学 · 材料科学
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COMPOSITES PART B-ENGINEERING · 2024 · IF 12.7

Vibration-damping, fire-retardant, smoke-suppressing, and anti-dripping bio-based polyurethane composites enabled by functionalized UiO-66-NH2 nanomaterials

Tianchen Zhang,Yijiao Xue,Fei Song,Zheng Pan,Meng Zhang,Yonghong Zhou

As we all know, in the field of safety protection, it is crucial to develop protective materials with fire-retardant and vibration-damping properties. However, it is a challenging task to integrate different properties into a single polymer. To meet this challenge, we successfully developed a functionalized nano flame retardant (UiO-66-NH 2 @DOPO) by modifying UiO-66-NH 2 with 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO). This flame retardant was then incorporated into a porous polyurethane foam (MPUF) synthesized from a bio-based polyol, resulting in a bio-based MPUF composite with excellent vibration-damping, fire-retardant, smoke-suppressing, and anti-dripping properties. Due to the intumescent fire-retardant system formed by UiO-66-NH 2 and DOPO, when the additional amount of UiO-66-NH 2 @DOPO reached 25 %, the LOI value of the MPUF composite material was increased to 31.2 %, and the total smoke production (TSP) was reduced by 80.64 %. In addition, it obtained a V-0 rating in the UL94 test and exhibited excellent anti-dripping properties. In addition, owing to the reinforcement effect and stress dissipation of UiO-66-NH 2 @DOPO, the MPUF composites exhibited excellent energy dissipation and vibration-damping properties (maximum loss factor of 1.32 at 1.0 Hz). This new bio-based MPUF composite material has broad application prospects. It can become an innovative self-supporting vibration-damping and protective material in sports, transportation, and aerospace.

研究领域: 材料科学 · 安全工程 · 化学工程
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CHIRALITY · 2025 ·Vol. 37 ·期 8 ·e70049 · IF 3

Chiral Post-Modification of UiO-66-NH2 on Gas Chromatography Chiral Separation

Jia Huang,Yizhuo Ma,Maria Abbasi,Junzhe Qin,Mingxuan Li,Zi Yang,Xuran Sun,Wei Wang,Zhen Wang,Fang Liu,Luo Aiqin,Lina Geng

As enantiomers can have different pharmacological and toxicological impacts even though they have the analogous chemical composition, efficient chiral separation is crucial. Chromatography is one of the primary methods for separating enantiomers, and the key to chromatographic separation lies in the chiral stationary phase (CSP). Chiral porous materials have emerged as innovative chiral stationary phases and garnered extensive attention. Zr based MOF materials, have been regarded as one of the most stable metal–organic framework (MOF) materials. In this paper, after grafting with L-proline, UiO-66 was used for the first time for chiral gas chromatography separation. The newly developed CSP provided high resolution for xylenes within only 2–3 min. For substances like linalool, α-pinene, and xylenes, the UiO-66-NH 2 -L-Pro–coated capillary column acquired bas3ic resolution and showed outstanding enantiomeric and positional isomer isolation. Comprehensive characterizations, including SEM, XRD, FT-IR, TGA, N 2 adsorption–desorption isotherms, CD spectra, and XPS, were conducted to analyze the material stucture and chiral recognition mechanism. The chiral separation relies on transient diastereomeric complexes formed between L-proline and enantiomers, stabilized by hydrogen bonding, intermolecular forces, and steric constraints within UiO-66's micropores. These interactions enforce enantioselective discrimination via the pore's stereochemical filtering, enabling chiral resolution. This study is expected to provide significant value for both chromatographic chiral separation and large-scale chiral substance separation.

研究领域: 分析化学 · 色谱学 · 材料科学 · 分离科学 · 有机化学
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Surfaces and Interfaces · 2025 · IF 6.3

Synthesis and application of UiO-66-NO2@Ag/AgCl nanocomposite as photocatalysts for water remediation

Xiao Ling,Xiaofeng Guo,Ke Wang,Ziming Huang,Zhixuan Mo,Huibo Qin,Linhai Duan,Xiuhong Meng,Hui Wang

Photocatalytic degradation of organic pollutants in water represents a highly promising strategy for environmental remediation. However, conventional photocatalysts are hampered by their inefficient employment of visible light energy and the propensity of photoinduced charge carriers to undergo recombination. To overcome these limitations, Z-scheme photocatalyst UiO-66-NO 2 @ Ag/AgCl (UiO@Ag-X, where X denotes the Ag/AgCl content) composites were designed and prepared. The crystal structure, morphology, photocatalytic performance, light absorption capacity, and carrier separation efficiency were systematically tested. Optical and electrochemical measurements revealed that the incorporation of Ag/AgCl enhanced the segregation and transfer efficiency of charge, which is crucial for boosting photocatalytic activity. These improvements directly contributed to the enhanced degradation efficiency observed in subsequent experiments. In experiments using methyl violet (MV) as the model pollutant, the photocatalytic degradation performance of UiO@Ag-X samples was evaluated. Among these samples, UiO@Ag-50 achieved a remarkable degradation efficiency under light irradiation. Moreover, the corresponding kinetic rate constant was about 0.04724 min -1 , which was higher than that of UiO-66-NO 2 . Quenching experiments were employed to investigate the mechanisms related to photocatalysis. The results show that hydroxyl radicals play an important role in the degradation of MV.

研究领域: 环境科学 · 材料科学 · 化学工程 · 纳米技术
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JOURNAL OF SOLID STATE CHEMISTRY · 2024 · IF 3.2

Direct Z-scheme charge transfer Bi2O3/UiO-66-NH2 heterojunctions for boosted photocatalytic degradation of tetracycline hydrochloride in different water systems

Shipeng Liao,Muhammad Arif,Xingyue Qian,Guangyu He

The development of hybrid heterostructure photocatalysts with enhanced visible light absorption capacity holds significant importance in environmental remediation. However, the challenge persists in exploiting strong visible-light responsive photocatalysts with both high efficiency and stability. Herein, we successfully synthesized a hybrid Z-scheme heterojunction of Bi 2 O 3 and UiO-66-NH 2 (Bi 2 O 3 /UiO-66-NH 2 ) through a simple hydrothermal route. The visible light photocatalytic performance of Z-scheme Bi 2 O 3 /UiO-66-NH 2 heterojunction is systematically evaluated for persistent antibiotic tetracycline hydrochloride (TC-HCl) both in the clean and real water matrix. All heterojunction catalysts exhibit superior photodegradation capabilities compared to pristine Bi 2 O 3 and UiO-66-NH 2 . The optimal ratio of the two components heterojunction (BUN-150), in particular, demonstrates the highest removal efficiencies for TC-HCl (95 %) within a 90-min timeframe. This remarkable photocatalytic performance is credited to the Z-scheme charge transfer occurring at the interface of Bi 2 O 3 and UiO-66-NH 2 in Bi 2 O 3 /UiO-66-NH 2 heterojunction. The active species experiments and electron paramagnetic resonance analyses are conducted to identify the active reactive species during the TC-HCl degradation (·OH, h + , and ·O 2 − ), and a precise photocatalytic degradation mechanism is explained. Additionally, the photodegradation intermediates of TC-HCl are detected using the HPLC-MS analysis to explain the degradation pathways of TC-HCl. This research paves the way for the development of novel Z-scheme Bi 2 O 3 -based heterojunction catalysts for outstanding photocatalytic applications.

CAS / MDL: 64-75-5
研究领域: 环境科学 · 材料科学
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INDUSTRIAL CROPS AND PRODUCTS · 2024 · IF 5.6

Preparation of multifunctional flame-retardant wood composites by crosslinking chitosan-based polymers with phytic acid functionalized UiO-66-NH2

Yaohong Yang,Yuefeng Huang,Xinjie Yang,Li Liu,Peng Wang,Zhenqiang Kan,Wei Bi,Kaimeng Xu,Guanben Du,Lianpeng Zhang

Bio-based composites can mitigate the pollution issues linked to petroleum-based materials due to their eco-friendly properties. On the other hand, bio-based functionalized metal-organic frameworks have gained attention in the field of flame retardants due to their multi-pathway flame retardant mechanism and environmentally friendly synthesis process. However, its application in wood industry is less. In this work, a novel functional adhesive and coating (ACS-MACS/PA-UiO66-NH 2 ) was developed by using phosphorus-rich biomass phytate functionalized metal-organic framework (MOF) PA-UiO66-NH 2 as a flame retardant and mixed with modified chitosan. Furthermore, using ACS-MACS/PA-UiO66-NH 2 and three-layer wooden boards, a tight cross-linked network was formed through hot pressing dehydration and condensation reactions to prepare multifunctional wood composites. The experimental results indicated that the mechanical properties of the multifunctional wood composites are excellent. Additionally, these wood composites exhibit high levels of charring and graphitization, leading to excellent flame retardancy. The preparation process of these multifunctional wood composites is straightforward, and their excellent properties provide a foundation for the development of high-performance green composite materials.

研究领域: 材料科学 · 生物质工程
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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

Mxene nanohybrids assembled with phytic acid-modified UiO-66 toward mechanically reinforced, fire-resistant and Smoke-suppressed epoxy composites

Kaili Gong,Lian Yin,Zilong Wu,Keqing Zhou,William W. Yu

Given the good structural and compositional characteristics, there are considerable trends towards optimizing the architectures of two-dimensional materials to work for high-performance flame-retardant polymeric materials. Herein, considering the promising features of Ti 3 C 2 T x MXene, phytic acid-modified UiO-66 (PA-UIO) was self-assembled onto MXene nanosheets (MXene/PA-UIO) using electrostatic interactions. The resulting nanohybrids presented good interfacial interactions and dispersion in epoxy matrix, opening up the possibility of simultaneously improving the mechanical and flame-retardant properties of the composites. Consequently, epoxy composites with 2 wt% MXene/PA-UIO achieved elevated mechanical properties and enhanced thermal properties, reflected by the increased storage modulus and tensile strength, as well as the declined rate of mass loss (R max , 28.3% reduction rate). Also, the addition of MXene/PA-UIO nanohybrids led to the drops in peak heat release rate (PHRR), peak smoke production rate (PSPR), peak CO production rate (PCOP) and peak CO 2 production rate (PCO 2 P) of 32.0%, 36.5%, 33.8% and 38.6% respectively, compared to those of pure epoxy. Meanwhile, a smoke factor (SF) with 47% drop rate was obtained, accompanied by significantly decreased gas-phase products, verifying the superior heat-reducing, smoke-suppressing and toxic fume-attenuating effects of the nanohybrids. The synergistic effects between MXene and PA-UIO realized the “3-in-1” fire-safety epoxy nanocomposites in mechanical properties, flame retardancy and smoke/toxic fume-suppressing effects. The performance enhancement was mainly attributed to the dehydration charring of phosphorus-containing acid, catalytic charring of transition metal derivatives, quenching effects of phosphorus radicals and dilution of non-flammable gases, as well as the barrier effects of the nanosheets.

研究领域: 材料科学 · 高分子化学
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