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ACS Sustainable Chemistry & Engineering · 2025 · IF 7.3

Organic–Inorganic Composite Strategy for Fluorinated Waterborne Polyurethane (WPU)@ZIF-8/Ti3C2Tx Coatings to Achieve Superior Anticorrosion Properties for Bronze Protection

Wenling Wu,Xuan Zhang,Anding Shao,Gang Zhen,Yang Cheng,Xiangfei Wang,Jianfeng Zhu,Hongjie Luo

The corrosion of ancient bronze relics and protection measures after excavation are of great importance to the study of historical and cultural heritage. At present, the bionic superhydrophobic surface anticorrosive coating is one of the main anticorrosive measures of bronze cultural relics. It aims to construct a barrier to prevent the contact between corrosive media and bronze to reduce the invasion of corrosive media. However, due to structural defects such as micropores in a single organic coating, corrosive media (O2, Cl–, and H2O) can penetrate the coating to the metal matrix. Nanomaterials such as MXenes and metal–organic frameworks (MOFs) can fill structural defects such as microholes and microcracks of the coating, thereby improving the density of the coating. Therefore, to improve the performance of organic waterborne polyurethane (WPU) coatings with good chemical protection, nanomaterial ZIF-8/Ti3C2Tx was introduced based on the organic–inorganic hybrid theory. Finally, the coating was modified by 1H,1H,2H,2H-perfluorodecyltriethoxysilane, and the organic–inorganic composite coating was prepared. Characterizations of the composite coating were performed via Fourier transform infrared spectroscopy, X-ray diffraction, Brunauer–Emmett–Teller method, field-emission scanning electron microscopy/energy-dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy. Colorimetric measurements and reversibility experiments of the coating were also evidenced. According to the electrochemical impedance spectroscopy assessments, the |Z|0.01 Hz value of the F-WPU@ZIF-8/Ti3C2Tx composite coating in a 3.5 wt % NaCl solution, which was higher compared to other composite coatings. Moreover, the icorr value of the F-WPU@ZIF-8/Ti3C2Tx (3.344 × 10–6 A cm–2) composite coating is reduced by 2 orders of magnitude compared with F-WPU@ZIF-8 and F-WPU@Ti3C2Tx coatings. As a result, this organic–inorganic F-WPU@ZIF-8/Ti3C2Tx composite coating has good anticorrosion properties to bronze without causing an obvious color difference change and has potential application prospects in various metal material fields.

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SEPARATION AND PURIFICATION TECHNOLOGY · 2018 · IF 3.927

Viscosity-driven in situ self-assembly strategy to fabricate cross-linked ZIF-90/PVA hybrid membranes for ethanol dehydration via pervaporation

Zhong Wei,Qiang Liu,Chunlin Wu,Heyun Wang,Hao Wang

In this study, poly(vinyl alcohol) (PVA) hybrid membranes with zeolitic imidazolate framework-90 (ZIF-90) particles were fabricated by the viscosity-driven in situ self-assembly of ZIF-90 particles in a PVA matrix and were employed for ethanol dehydration via pervaporation (PV) technology. By this method, the size-controlled and well-distributed ZIF-90 particles were successfully embedded into PVA membranes. Based on the cross-linking reactions between the ZIF-90 particles and the PVA matrix, the ZIF-90/PVA hybrid membranes demonstrated higher mechanical strength, swelling resistance, and a high separation performance for ethanol dehydration. The ZIF-90/PVA hybrid membranes were characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, X-ray diffractometry, thermogravimetric analysis, a mechanical test, and water contact angle measurements. The effects of the ZIF-90 particle size, loading level, thermal treatment temperature, operation temperature, and the feed compositions of the PVA hybrid membranes on the PV performance were systematically explored. Accordingly, the hybrid membranes exhibited excellent water permeability and selectivity for water–ethanol mixture separation. Specifically, the ZIF-90/PVA hybrid membrane (M-8), which was treated thermally at 130 °C, exhibited its optimal PV performance at a flux of 268 g/(m 2 h) and a separation factor of 1379 for the PV dehydration of the 90 wt% ethanol aqueous solution at 30 °C. The ZIF-90/PVA hybrid membranes exhibited excellent potential in the PV application for ethanol dehydration.

CAS / MDL: 9002-89-5
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Cellulose nanocrystals as bridges to construct CNCs@ZIF-8 3D network with topological chirality for realizing efficient photocatalytic reduction of CO2

Jing Wang,Wenlei Wang,Yao Deng,Ting Yang,Zhen Zhang,Hui Wang,Yiqiang Wu

Chiral nanomaterials typically exhibit special optical activities, such as optical rotation and chiral photomechanics, and have enormous potential for applications in molecular chiral photocatalysis and other fields. In this work, cellulose nanocrystals (CNCs) were obtained from renewable and affordable bamboo resources through the steps of delignification, hemicellulose removal and acid digestion. Meanwhile, ZIF-8 materials with truncated rhombic dodecahedral structure were obtained by liquid-phase synthesis from Zn 2+ coordinated with 2-methylimidazole (2-MiM). And then, the topologically chiral CNCs@ZIF-8 3D network was successfully constructed by using CNCs as a bridge to graft with ZIF-8 through the formation of Zn–N–S and Zn–O–S bonds. The photoreduction yield of CO 2 to CO by CNCs@ZIF-8 (α = +21.290) with topological chirality was 301.16 μmol −1 ·g −1 , which was 9.43 times that of ZIF-8 (α = 0.000). Density functional theory (DFT) calculations confirm that Zn–O–S with a larger bond angle (118.0°) was conducive to charge accumulation. Photoelectric test results show that CNCs can improve the electron transport ability and reduce the rate of photogenerated electron-hole complexation in ZIF-8. This work elucidated the mechanism of chiral auxiliaries in photocatalytic reduction of CO 2 and provided a new strategy for photocatalytic reduction of CO 2 .

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Journal of Environmental Chemical Engineering · 2025 · IF 7.2

Construction of inter phase covalent bonding in ZIF-7-NH2(x) particles doped PA TFN membranes for improved reverse osmosis performance

Yang Gao,Yuyang Wang,Yanlin Jiang,Chaojie Bai,Zuoqun Zhang,Yawen Zhao,Congjie Gao,Lixin Xue

To improve interface compatibility between ZIF-7 particles (PTs) and polyamide (PA) and reverse osmosis (RO) performance of thin film nano-composite (TFN) membranes, ZIF-7-NH 2 (x) particles (PTs) with different levels of -NH 2 substitution were synthesized by reacting Zn(NO 3 ) 2 with mixed ligand under different preparation conditions. The impact of their residual surface functional groups (SFGs) on the formation of inter-phase covalent bonds (ICBs) in PA separating layers were investigated relating to the inter-phase compatibility and salt rejection performance of the formed composite RO membranes. Doping ZIF-7-NH 2 PTs with ICBs could avoid the expansion of PA in acidic condition. Surprisingly high chemical stability was observed for ZIF-7-NH 2 PTs wrapped in the PA separating layers in TN membranes in the pH range of 2–13. TN(50)-0.15 membranes with strong ICBs showed 3 times higher water flux of 76 L·m −2 ·h −1 under 5.5 MPa at a high salt rejection of 98.7 %.

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POLYMER DEGRADATION AND STABILITY · 2024 · IF 6.3

Core-shell flame retardant/APP-PEI@MXene@ZIF-67: A nanomaterials self-assembly strategy towards reducing fire hazard of thermoplastic polyurethane

Mei Wan,Congling Shi,Lei Chen,Lei Deng,Yueping Qin,Honglei Che,Jingyun Jing,Junyi Li,Xiaodong Qian

Ammonium polyphosphate (APP) is the most commercially valuable phosphorus-based flame retardant, but poor interaction with the polymer interface limits the flame-retardant efficiency. In this work, a new type of multi-layered nanomaterial coating APP (APP-PEI@MXene@ZIF-67) was prepared and introduced into thermoplastic polyurethane (TPU) polymers by a simple and green assembly strategy. The effects of different loading shells of modified APP on the flame retardancy of TPU composites were investigated, as well as their gas/condensed phase thermal degradation products and their flame-retardant mechanisms. The results showed that APP-PEI@MXene@ZIF-67 was more favorable for catalytic char formation than APP, and the residual char formed by its composites was denser and more continuous. Compared with the pure TPU, the pHRR, THR, pSPR, and TSP of TPU/APP-PEI@MXene@ZIF-67–2BL composites were decreased by 72.75 %, 87.25 %, 59.58 %, and 85.97 %, respectively, which significantly reduced the heat and smoke release during the combustion process. The gas-phase and condensed-phase flame retardant mechanisms synergized to construct a possible approach to address the fire risk and heat/smoke hazards of TPUs and promote the extensive application of TPU polymers.

CAS / MDL: 7789-24-4
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JOURNAL OF CATALYSIS · 2024 · IF 6.5

A novel and facile ultraviolet-induced photo-reduction for preparing oxidase-like AuNCs@H2N-ZIF-8 composites in alcohol-water solutions

Xin-Yu Chang,Hong-Wei Li,Yuqing Wu

The composites of H 2 N-ZIF-8 supported gold nanoclusters (AuNCs@H 2 N-ZIF-8) were prepared by UV-induced photochemical reduction method in the methanol–water solution. The photochemical reaction was attributed to the generation of free radical as. CH 2 ·–OH, which reduced Au(III) to Au(0) and produced monodisperse AuNCs (<2.5 nm) in the mesoporous of H 2 N-ZIF-8. The generated AuNCs@H 2 N-ZIF-8 show oxidase-like properties to catalyze the oxidation of TMB, ABTS and OPD under mild conditions. Besides, the mechanism study by EPR shows that the composites can promote oxygen to generate singlet oxygen ( 1 O 2 ) and superoxide radicals ( ·O 2 - ), endowing it excellent catalytic activity of oxidation. Further studies revealed that the large number of exposed small AuNCs in the mesoporous pores of H 2 N-ZIF-8 and the highly active 211 crystalline facets formed at the edges contribute to the ROS generation intrinsically. Therefore, the present study demonstrates the significance of photochemical reduction method to prepare highly efficient oxidase-like materials, opening up a new avenue to construct noble metal materials as ultra-small nanozyme.

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Materials Today Chemistry · 2025 · IF 6.7

Based on the synergistic effect of cobalt alginate/ZIF-67 strengthening the combustion and mechanical properties of ammonium perchlorate-based propellant

Haozhe Li,Xiandie Zhang,Heng Xu,Xuxu Cui,Zhijie Fan,Zhen Liu,Xiaode Guo

The pursuit of high combustion performance and good mechanical properties is an urgent need for the development of composite solid propellants. Ammonium perchlorate/cobalt alginate/ZIF-67 (AP/Co-A/ZIF) composites were successfully synthesized by droplet and solution assembly method. The layered porous structure of Co-A increases the reaction site between AP and ZIF-67 so that is oxidized to produce Co 3 O 4 earlier, and further accelerate the heat release of the system. carbonized porous framework formed by the decomposition of Co-A has kind electrical and thermal conductivity, and makes Co 3 O 4 produced by the decomposition of ZIF-67 and Co-A well dispersed on the framework, achieving efficient charge transfer. The synergistic catalysis of Co-A/ZIF makes the low and high temperature decomposition stages of AP combine, which the high temperature decomposition temperature greatly reduced with a higher heat release. After being applied to AP-based propellants, the organic porous structure of Co-A shortens the heat transfer distance and plays an obvious combustion-supporting effect, while ZIF-67 accelerates the energy release rate to burn more violently, so that considerably improves the ignition capacity and combustion rate of the propellant. In addition, the reaction of Co-A and TDI effectively strengthens the interface interaction between AP and binder matrix, alleviates the dewetting phenomenon, and enormously improves the mechanical properties of the propellant. As an efficient composite nonmetallic combustion catalyst, Co-A/ZIF not only exhibits strong synergistic catalytic ability for propellant combustion, but also effectively improves the mechanical properties of the propellant. It provides a development direction for building a new catalyst to enhance the comprehensive performance of AP-based solid propellant.

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TALANTA · 2024 · IF 5.6

A highly sensitive and selective SERS sensors based on Au@PATP@Ag@ZIF-8 for the detection of phosphate in water

Yueshou Zhang,Lichun Yang,Yulin Xu,Haiting Ren,Shi Yin,Yan Sun,Yongjun Hu

Rapid and sensitive detection of phosphate is of great significance for ensuring water safety and preventing eutrophication. In this study, we prepared Au@PATP@Ag NRs core-shell structures using 4-aminothiophenol (PATP) as an internal standard signal molecule to enhance the stability of the SERS signal. Based on the phosphate-induced decomposition of ZIF-8 and the protective effect of ZIF-8 on the internal Au@PATP@Ag NRs, a phosphate SERS sensor (Au@PATP@Ag@ZIF-8) with high sensitivity, selectivity and stability was designed. This method exhibited a good linear range of 0.1–125 μM and a detection limit of 30 nM. Furthermore, the developed sensor (Au@PATP@Ag@ZIF-8) was effectively applied to assess PO 4 3− in tap water samples, achieving recoveries between 97.44% and 104.54%. With its simple, fast and sensitive features, this method of phosphate detection in water provides a direction for the research and practical application of phosphate detection.

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ANALYTICA CHIMICA ACTA · 2024 · IF 5.7

3D printed microplasma optical emission spectrometry coupled with ZIF-8 based dispersive solid-phase extraction for field analysis of waterborne arsenic

Jiahui Yang,Yao Lin,Xi Wang,Yuanyuan Li,Yurong Deng,Chengbin Zheng

Background Arsenic contamination of drinking water has become a public health challenge over the world, particularly in Bangladesh, India, and China. Compared to the most used field test kits of waterborne arsenic, miniature microplasma atomic spectrometry retains advantages of accuracy, elemental specificity, and less matrix interference. Despite increased interest in arsenic detection by using miniature microplasma spectrometry, the improvements of its analytical performance, manufacturing cost and consistency still remain significant challenges. Results Herein, a miniature, battery-operated, and integrated hydride generation point discharge optical emission spectrometer (HG-μPD-OES, 116 mm length × 92 mm width × 104 mm height) was printed with a simple 3D printer and used for the highly sensitive and element-specific determination of arsenic by coupling to a dispersive solid-phase extraction (d-SPE) using zeolitic imidazolate framework-8 as adsorbent. The d-SPE simplifies sample treatment, significantly alleviates the interference arising from transition metal ions and improves sensitivity. A LOD of 0.07 μg L −1 for arsenic was obtained with relative standard deviations (RSDs, n = 11) better than 3.8 %. Significance The 3D printing technique significantly improves the manufacturing cost and fabricating consistency of HG-μPD-OES. LOD were remarkably improved 27-fold compared to those obtained by conventional HG-μPD-OES, providing a promising method for the reliable, sensitive, and convenient field analysis of waterborne arsenic even its concentration as low as 0.2 μg L −1 . The practicability and accuracy of the proposed method have been successfully verified via the field analysis of waterborne arsenic in a Certified Reference Material (GBW(E)080390) and a series of river and lake water samples.

CAS / MDL: 693-98-1
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Molecular Catalysis · 2024 · IF 3.9

Preparation of 30%PMoV2@MOF@mSiO2 (MOF = MIL-101, HKUST-1, UiO-67, ZIF-8) catalysts and their oxidative desulfurization performance

Pushuang Xing,Cong Li,Yixin Chen,Rong-Lan Zhang

PMoV 2 was encapsulated in four MOFs (MIL-101, HKUST-1, UiO-67, ZIF-8) with different cavity sizes and window sizes using a hydrothermal synthesis method. Then, a layer of mesoporous silica was coated on the surface of the MOFs to obtain four designed three-layer encapsulated catalysts 30%PMoV 2 @MOF@mSiO 2 . The physicochemical properties of the catalysts were characterized through various characterization methods, and the influence of different MOF window sizes of the four catalysts on the removal rate of four thiophene sulfides was investigated. The optimal reaction conditions were also explored for the optimal catalyst. The results indicate that under simulated fuel of 2400 ppm, 30%PMoV 2 @UiO-67@mSiO 2 owns the highest catalytic activity. Under optimal conditions, the total removal rate of four thiophene compounds was 91.52 %, and after ten cycles, the efficiency could still reach 86.24 %. This is attributed to the sufficient cavity size of UiO-67, which provides assurance for the loading of PMoV 2 and the large window size, making it possible for the smooth reaction between sulfides and PMoV 2 .

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JOURNAL OF MEMBRANE SCIENCE · 2025 · IF 9

PPS/TA-PEI/CaAlg/ZIF-8 composite membranes with under-liquid dual superlyophobicity for on-demand separation of oil-water emulsions

Shiwei Tian,Yaqi Zhang,Qiankun Sha,Yixuan Wang,Xingxiang Zhang,Xuhuan Yan,Na Han

Polyphenylene sulfide (PPS) membrane materials have attracted significant attention for separating oily wastewater due to their remarkable separation precision and permeation capability. Nevertheless, the inherent hydrophobic characteristics result in a single wetting property, which restricts their broad applicability in treating diverse types of oily wastewater. In this study, the PPS/TA-PEI/CaAlg/ZIF-8 composite membranes exhibit outstanding under-liquid dual superlyophobicity, which were formed via constructing a composite coating containing polyphenol-polycation and calcium alginate (CaAlg) hydrogel, and assembling ZIF-8 nanocrystals with suitable surface chemistry. Through the solvent pre-wetting approach, the surface wettability of the PPS composite membranes can be flexibly transitioned between under-water superoleophobicity and under-oil superhydrophobicity, thus realizing on-demand separation of oily wastewater. It is noteworthy that the treatment efficiency of the PPS/TA-PEI/CaAlg/ZIF-8 composite membranes for the various oil-water mixtures (surfactant-free) and emulsions (stabilized by surfactants) attained greater than 98.1%. Meanwhile, the rapid transport capability of diverse types of oil-water emulsions can also be exhibited, with a permeance of 1652.4 L m -2 h -1 bar -1 for water-in-oil (W/O) emulsions and 2087.5 L m -2 h -1 bar -1 for oil-in-water (O/W) emulsions. In addition, the PPS composite membranes demonstrated outstanding anti-fouling capacity, recyclability, and switchable separation capacity. This work extended the utilization of the PPS membrane material in the controllable treatment of oily wastewater.

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MICROPOROUS AND MESOPOROUS MATERIALS · 2024 · IF 4.8

Rich active sites ZIF-8 base on imidazole-based deep eutectic solvents for rapid adsorption of acid fuchsin and competitive adsorption

Yiwen Li,Shikuan Xu,Yangyang Zhang,Rui Du,Rong Li,Yanjun Xing

MimDES-ZIF-8 with rich active sites as positive charges and metal coordination sites were prepared based on imidazole based deep eutectic solvent (MimDES) using interface permeation method. 2-Methylimidazole (2-Mim) simultaneously acted as a hydrogen bond acceptor (HBA) in MimDES (hydrogen donner was 1,6-hexanediol) and an organic ligand in MimDES-ZIF-8, affecting the coordination of ZIF-8 during permeation. Four different zinc salt solutions (ZnCl 2 , Zn(NO 3 ) 2 ·6H 2 O, Zn(OAc) 2 ·2H 2 O, ZnSO 4 ·7H 2 O) were permeated into MimDES to obtain MimDES-ZIF-8 with different morphologies. All MimDES-ZIF-8 had higher Zn/N ration (>0.25), specific surface area and surface positive charges. The dye adsorption results indicated that MimDES-ZIF-8 showed high adsorption efficiencies for acid fuchsin (all exceeded 97.75 % under pH 7.5) and a fast adsorption rate (exceeding 93 % in 5 min and reaching equilibrium in 60 min). Among MimDES-ZIF-8, the adsorption capacity of ZIF-8-C was 4845.3 mg/g. After five cycles of adsorption, the AF removal efficiency of ZIF-8-C remained over 93.23 %. Moreover, ZIF-8-C also had good adsorption capacity for anionic dyes CR, cationic dyes MB and BB. The adsorption process aligned well with both the Langmuir model and the pseudo-second-order kinetic model. Based on FTIR, XPS, and electrostatic potential calculation, the adsorption mechanism was elucidated.

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