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JOURNAL OF FOOD COMPOSITION AND ANALYSIS · 2024 · IF 4

Analysis, distribution, and health evaluation of 8 biogenic amines in Chinese mackerel products by CoFe2O4/MEG solid phase extraction-HPLC

Xinying Guo,Feng Chen,Shaocong Pan,Huamin Sun

A CoFe 2 O 4 /MEG solid-phase extraction combined with high performance liquid chromatography was used for determination of 8 biogenic amines (Bas) in canned Spanish mackerel products. A new comprehensive evaluation system, including dietary exposure, food safety index, chemical quality index and biogenic amine index, was used for investigating the pollution distribution, exposure and health assessment of BAs in four sea areas/provinces of China. The pollution levels in the Yellow Sea-Jiangsu, Bohai Sea-Shandong, Yellow and Bohai Sea-Liaoning regions were equivalent, with ∑8BAs equalling 34.7–36.5 mg/kg, while in the South China Sea-Guangdong region ∑8BAs was lowest at 18.9 mg/kg. The concentration range of ∑8BAs and ∑4BAs were ND (not detected)-113 mg/kg and ND-80.8 mg/kg, respectively. All results showed that the main components of BAs were putrescine, histamine, and spermine, with detection rates ranging from 23.1% to 42.3%. The dietary exposure level range of 8 BAs was 85.8–266 μg∙kg −1 ∙d −1 , IFSc was 0.00800–0.0248, CQI values range in the four regions was 1.21–3.93, with a mean CQI of 1.98. The total value of BAI ranges ND-0.840 mg/kg, with a mean BAI of 20.3 mg/kg. Statistical analysis showed that the overall health risk of BAs exhibits different trends in terms of gender, age, and region.

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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

A novel ZIF-8@cellulose composite monolithic carbon via a facile template-free strategy for selective and efficient CO2 adsorption

Yu Shu,Longfei Qiao,Jialong Geng,Cong Li,Bang Chen,Qidong Wang,Hiroshi Uyama,Yehua Shen

In this work, hierarchically ZIF-8@Cellulose acetate composite monolithic carbon (ZCMC) was fabricated for the first time by combining a template-free thermally induced phase separation (TIPS) method with in-situ ZIF-8 crystals doping followed by KOH activation. By altering ZIF-8 content and activation temperature, a series of ZCMC samples were prepared in order to analyze the effect of pore structure and surface chemical characteristics on CO 2 adsorption. The optimal sample of 20-ZCMC-800 exhibited the largest CO 2 uptake of 7.30 (0 °C) and 4.26 mmol/g (25 °C) at 1 bar, which was competitive with the majority of the reported porous carbons. Additionally, the CO 2 adsorption capacity after 10 cycles still remained at 96 % of its initial value and the ideal adsorption solution theory (IAST) CO 2 /N 2 selectivity was 21.31 at 25 °C, indicating excellent recyclability and good selectivity. Furthermore, it was found that the CO 2 adsorption capacity was considered to be linear relationship with micropore but independent on BET specific surface area. The contributions of N-containing functional groups and ZnO crystals created from ZIF-8 pyrolysis at high temperature for CO 2 adsorption were thoroughly discussed under density functional theory (DFT) and grand canonical Monte Carlo (GCMC). The results showed that pyrrole-N group contributed significantly to CO 2 adsorption by hydrogen bonding and Lewis acid-base interactions, while the ZnO crystals displayed the strong interaction with CO 2 by the chemisorption process. The CO 2 adsorption performance of ZCMC was mostly determined by the joint effect of micropore structure and surface chemical compositions. The thermodynamic parameters of Q st ranged from 23.03 to 33.23 kJ/mol, revealing the CO 2 adsorption still belonged to the scope of physisorption process. More importantly, the novel and feasible strategy presented herein is expected to provide an innovative approach for the design and discovery of ZIFs-based composite carbon materials for efficiently CO 2 adsorption.

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Food Bioscience · 2025 · IF 5.9

A label-free electrochemical aptasensor combined Au/Ag@ZIF-8 and dual amplification strategy for sensitive detection of β-lactoglobulin

Tao Lu,Zhiguang Suo,Min Wei,Huali Jin,Yong Liu,Baoshan He,Renyong Zhao

β-lactoglobulin (β-LG) is a major allergen in milk what can provoke intense allergic reactions. Therefore, an accurate and efficient method is required for sensitive detection of β-LG. A label-free electrochemical aptasensor utilizing Au/Ag@ZIF-8 and dual amplification strategy has been designed for the detection of β-LG. Au/Ag@ZIF-8 nanocomposite is used as the electrode modification material, which has abundant relative surface area and exceptional conductivity behavior, and it can also serve to immobilize DNA strands. By combining RecJf exonuclease and hybridization chain reaction (HCR) dual amplification strategy, an apparent enhancement of electrochemical signal is obtained. β-LG undergoes target cycling in the effect of RecJf exonuclease, which dislodges complementary strand cDNA and further triggers HCR to provide a large number of sites for methylene blue embedding. The detection range of this aptasensor is 0.01–1000 ng/mL in the optimal detection conditions, with a limit of detection (LOD) of 5.37 pg/mL. The constructed electrochemical aptasensor possesses the superiorities of good specificity, preeminent accuracy and satisfied stability in the detection of β-LG. Moreover, it also demonstrates satisfactory detection performance in the detection of real samples, which indicates that the electrochemical aptasensor has a broad application prospect in protecting food safety and health.

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MICROCHIMICA ACTA · 2025 ·Vol. 192 ·期 2 ·1-13 · IF 5.3

Preparation of CHS-Fe3O4@@ZIF-8 peroxidase-mimic with an ultra-thin hollow layer for ultrasensitive electrochemical detection of kanamycin

Zhang Jiadong,Cui Yaoying,Dou Yanchao,Zhu Jingying,Ma Xiangyu,Guo Liming,Zhang Kai,Hao Nan,Feng Liangdong,Chen Yi

A highly sensitive and selective electrochemical biosensor was developed for the detection of kanamycin using a core-hollow-shell structured peroxidase-mimic nanozyme, CHS-Fe₃O₄@@ZIF-8. The synthesized CHS-Fe 3 O 4 @@ZIF-8 was characterized with scanning electron microscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy. It was found that the CHS-Fe 3 O 4 @@ZIF-8 exhibits excellent peroxidase-like activity due to  its ultra-thin hollow layer. Besides, CHS-Fe 3 O 4 @@ZIF-8 functionalized with complementary chains of kanamycin aptamer was anchored to the electrode surface via complementary base pairing with the kanamycin aptamer. Upon the presence of kanamycin, a strand displacement reaction was triggered leading to a reduction in the number of the CHS-Fe 3 O 4 @@ZIF-8, which slowed down the catalytic reaction of the substrate 3,3’,5,5’ -tetramethylbenzidine (TMB) facilitated by CHS-Fe 3 O 4 @@ZIF 8. Differential pulse voltammetry (DPV) was employed to measure and record changes in peak current resulting from catalytic oxidation product formation (oxidation product of TMB). The electrochemical signal exhibited a linear relationship with logarithmic variations in kanamycin concentration within a range spanning from 10 to 8000 pM and achieved an impressive detection limit as low as 7.52 pM. Furthermore, successful detection of kanamycin content in serum samples using this sensor demonstrated its good specificity and reproducibility. These findings indicate that the constructed electrochemical kanamycin sensor holds significant potential for practical applications. The biosensor demonstrated high selectivity, distinguishing kanamycin from other antibiotics, and exhibited good reproducibility, making it reliable for practical applications. The successful detection of kanamycin in serum samples further underscores the sensor’s potential for real-world applications, particularly in monitoring antibiotic residues in food products and clinical diagnostics. Graphical

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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Peroxymonosulfate activation by mineralized PVDF-TA@Co template based ZIF-67/8 electrospinning membranes for ofloxacin degradation under visible-light

Liusha Cen,Fan Yu,Chengcai Li,Guojin Liu,Wangyong Jin,Hailin Zhu,Yuhai Guo

Recently, heterogeneous catalysts prepared by two phase metals were commonly used to activate PMS degradation. However, the synergistic effects of Zn and other metals on the activation of PMS were infrequently studied. In this work, novel PVDF@TA-ZIF-67/8 nanofibers were prepared successfully by first mineralization and then in-situ growth. The prepared PTZ70 exhibited an evidently higher photocatalytic activity than PVDF, PTC, PTZ0, PTZ10 and PTZ100 to degradation OFX (96.5 %). The effects of the mass ratio of Co and Zn, PMS dosage, coexisting ions and organic solvents on the degradation of OFX were concretely investigated. The radical trapping experiment and mechanism analysis showed that the synergistic effect of Co and Zn played a key role in PMS activation, accelerating the generation of 1 O 2 and •O 2 – . Combining the discussion of influencing factors and LC-MS analysis, four OFX degradation pathways were illustrated. In particular, we observed that the degradation OFX of PTZ70 was only slightly reduced by 5.6 % after five cycling, indicating the reusability, good stability and high environmental suitability of PTZ70 performance . This study offers a novel path for the design of catalytic membranes with controllable heterogeneous metal doping.

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JOURNAL OF SOLID STATE CHEMISTRY · 2024 · IF 3.2

The effective adsorption separation of n-hexane/3-methylpentane by Vapor-Phase linker exchange of Zeolitic-Imidazolate Framework ZIF-8

Le Chen,An Xie,Nan Zhang,Jianjun Yin,Qun Chen,Mingyang He,Zhihui Zhang

Zeolitic-Imidazolate Framework 8 (ZIF-8), a porous crystalline absorbent, could be synthesized from the coordination reaction of zinc ions and 2-methylimidazole (2-mIM). ZIF-8 has a large specific surface area and a high adsorption capacity for n -hexane ( n HEX). However, ZIF-8 suffers from low selectivity for both linear and mono-chain alkanes. Therefore, ZIF-8 was modified through 2-mIM ligand being partly replaced by 2-nitroimidazole (2-nIM) through Vapor-Phase post-synthesis modification. The modified materials were denoted as ZIF-8-2-nIM-X (X = 24h, 48h, 72h). ZIF-8-2-nIM-X has a higher specific surface area and better thermal stability than ZIF-8. Further thermodynamic and kinetic calculations show that the affinity of hexane isomers on ZIF-8-2-nIM-X is spontaneous physical adsorption combined with an exothermic process. In contrast, kinetic studies show that the adsorption of hexane isomers on ZIF-8-2-nIM-X is a pseudo-second-order kinetic model. The batch and dynamic adsorption and separation properties of ZIF-8-2-nIM-X for hexane isomers were studied. The results of the one-component vapor adsorption equilibrium experiment show that ZIF-8-2-nIM-72h has the best adsorption separation coefficient at 293 K. The adsorption capacity of n HEX and 3-methylpentane (3MP) were 211.63 mg/g and 33.91 mg/g, respectively. Compared with ZIF-8 (selectivity coefficient: 1.08), the adsorption selectivity coefficient of the modified material is greatly improved. The adsorption selectivity coefficient of n HEX/3MP is 6.24 (ZIF-8-2-nIM-72h).

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LANGMUIR · 2025 · IF 3.9

Well-Dispersed ZIF-8 on Randomly Lamellar Clinoptilolite as an Adsorbent Showing Enhanced CO2/CH4 Selectivity for Biogas Gas Separation

Yingying Cheng,Yuanye Zhuang,Shiyang Bai,Meng Ge,Jihong Sun,Jingjing Sun,Xufeng Gong

The removal of CO2 from biogas is critically important for environmental protection and energy applications yet remains technically challenging in the chemical industry. In this work, novel composite adsorbents featuring ZIF-8 uniformly dispersed on randomly oriented clinoptilolite lamellae (LCP) were designed and fabricated through a straightforward composite method. The synthesis sequentially incorporated metal precursors into LCP via ion exchange and salt addition and then introduced organic ligands to generate ZIF-8. Comprehensive characterizations, including XRD, FT-IR, N2 adsorption–desorption isotherms, SEM, and TG analyses, confirmed the physicochemical properties and structural features of the composites. The synthesized Zn-LCP/ZIF-8 materials exhibited exceptional CO2/CH4 separation performance, demonstrating ultralow CH4 adsorption capacity (<0.1 mmol/g) coupled with superior CO2/CH4 selectivity (≈28). Complementary molecular simulations using Material Studio software provided mechanistic insights into the adsorption and separation behavior, which further confirmed the superiority of the composite structure in CO2/CH4 separation. These results establish an effective strategy for biogas purification, while offering new perspectives for enhancing the CO2/CH4 adsorption selectivity.

CAS / MDL: 25322-68-3 693-98-1
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Journal of Environmental Chemical Engineering · 2025 · IF 7.2

Fabrication of superhydrophobic PVDF composite membranes using modified ZIF-8 for efficient and stable membrane distillation: Mitigating fouling and wetting

Peiqing Zhang,Sihang Li,Fan Xiao,Yongfang Xiao,Yi Zhang,Zhongguo Shan,Zhenyu Li,Haihua Wang

Membrane distillation (MD) represents a promising advance in wastewater purification, contributing to the mitigation of water scarcity. Hydrophobic poly(vinylidene fluoride) (PVDF) microporous membrane is susceptible to wetting by low surface tension substances, leading to fouling. To address this, PVDF membrane was superhydrophobically modified using modified ZIF-8 to obtain two composite membranes, AZ/PVDF and Z@C/PVDF. AZ/PVDF and Z@C/PVDF composite membranes were prepared by coating more dispersible APTES-ZIF-8 and ZIF-8@MWCNT, respectively, onto the surface of PVDF membrane. The hydrophobicity of the composite membranes was regulated by silane types, fluorination methods, and fluorination time, resulting in reduced surface roughness and increased surface energy. The contact angles of AZ/PVDF and Z@C/PVDF were 154.2 ± 3.4° and 156.8 ± 4.2°, respectively. Both AZ/PVDF and Z@C/PVDF membranes demonstrated outstanding mechanical, thermal, and chemical stability. AZ/PVDF and Z@C/PVDF membranes outperformed PVDF membrane, extending operation times by 2 h and 3 h, respectively, without obvious NaCl crystals. Furthermore, Z@C/PVDF membrane exhibited superior resistance to wetting by SDS than AZ/PVDF and PVDF membranes, treating pickle brine via the direct contact MD (DCMD) process with a recovery rate of 30.2 % within 10 h. Overall, this research offers a promising approach to fabricating superhydrophobic composite membranes for high-salt brine treatment via DCMD.

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ChemistrySelect · 2025 ·Vol. 10 ·期 28 ·e00259 · IF 2

Fabrication of PVDF/ZIF-8 Composite Membrane via In-Situ Growth for Adsorptive Removal of Methyl Green from Aqueous Solution

Bo Yang,Hai Xing,Yang Xia,Xin Wang,Ningning Liu

Graphical ZIF-8 was synthesized through an in-situ growth method within a PVDF membrane matrix. The PVDF/ZIF-8 composite membrane was subsequently prepared via the phase inversion method using immersion precipitation. The ZIF-8 particles were uniformly distributed in the PVDF/ZIF-8 composite membrane. The widespread use of organic dyes in industrial processes has led to increasing environmental pollution due to the discharge of dye-contaminated wastewater, necessitating more efficient dye removal methods. In this study, a poly(vinylidene fluoride) (PVDF)/ZIF-8 composite membrane was fabricated via a phase inversion method using immersion precipitation, with ZIF-8 synthesized via in-situ growth within the membrane matrix. The composite membranes were thoroughly characterized using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and thermogravimetric analysis (TGA). The ZIF-8 particles were uniformly distributed in the PVDF/ZIF-8 composite membrane. The adsorption performance of the PVDF/ZIF-8 composite membrane was evaluated for methyl green (MG) removal. At 313 K with an adsorbent dose of 10 mg, the membrane exhibited an adsorption capacity of 172.30 mg g⁻¹ and a removal ratio of 87.21%, demonstrating that the incorporation of ZIF-8 significantly enhanced adsorption performance. Adsorption isotherm studies revealed that the process followed the Freundlich model, while kinetic analysis indicated a pseudo-second-order mechanism. Additionally, thermodynamic investigations suggested that the adsorption was endothermic and spontaneous. The major driving force for adsorption was identified as electrostatic interactions between the dye and the membrane. These findings highlight the potential of PVDF/ZIF-8 composite membranes for effective dye removal from wastewater.

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Carbon Letters · 2024 · IF 5.5

Upcycling of waste masks into carbon nanotubes combined with ZIF-8 for the detection of heavy-metal ions and nitrite

Han Tong,Piao Ying-Ai,Meng Long-Yue,Jin Biao

Food contamination with heavy-metal ions and nitrites poses a serious threat to human health. Consequently, the development of fast and sensitive platforms for detecting these contaminants is urgently needed. In this study, a novel sensing platform was developed by integrating carbon nanotubes generated by the pyrolysis of waste masks (WMCNTs) with ZIF-8 for the simultaneous detection of Cd 2+ , Pb 2+ , and nitrite. Specifically, the electronic structure of the WMCNT backbone was modulated by doping with B and N atoms. Nanoporous ZIF-8 was then grown in-situ on its surface to produce composites with enhanced electrical conductivities and large specific surface areas. This modification provided more active sites for the attachment of heavy-metal ions and nitrites. Under optimized conditions, the sensing platform exhibited a wide linear range with the Pb 2+ , Cd 2+ , and NO 2 − limits of detection of 2.68, 12.12, and 5.94 μM, respectively. Notably, the sensing platform demonstrated excellent anti-interference capabilities and effectively detected nitrites and heavy-metal ions in pickled foods. Graphical abstract

CAS / MDL: 7440-43-9 7439-92-1
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Journal of Environmental Chemical Engineering · 2025 · IF 7.2

Preparation of hydrophilic ZIF-8-NH2/PES mixed matrix membranes based on the co-solvent strategy for dye/salt separation

Chunlei Wang,Dawei Ji,Xuyong Tian,Hongye Lv,Xiuping Li,Tai Zhang,Haolong Xue,Chun Wang,Jingjing Yan,Changfa Xiao

Doping metal-organic frameworks into the casting solution is a common method for preparing mixed matrix membranes. However, metal-organic frameworks are prone to agglomeration and poor dispersion. This can lead to a decline in membrane performance. To address these issues, this work proposed “co-solvent synthesis and in-situ doping” strategy. In this strategy, N,N-Dimethylformamide, which was also the solvent in the casting solution, was chosen as the synthesis carrier for ZIF-8-NH 2 nanoparticles. The prepared ZIF-8-NH 2 suspension could be directly doped into the casting solution in situ. This process eliminated the drying and pre-dispersion steps. Research showed that with 0.5 wt% ZIF-8-NH 2 , the membrane's hydrophilicity significantly improved, with the water contact angle of 72.5°. The pure water flux reached 229 Lm −2 h −1 . Moreover, the retention rates of Congo Red and NaCl were 97.3 % and 3.5 % respectively, demonstrating excellent dye/salt separation. In particular, the flux recovery rate was maintained at more than 91 %, demonstrating good anti-fouling performance. This work provides a promising technical strategy for the efficient treatment of textile dyeing wastewater and resource recovery.

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Materials Today Chemistry · 2025 · IF 6.7

Multifunctional antibacterial-anti-inflammatory-osteogenic performance of ZIF-8/PDA composite scaffold for osteoporotic bone regeneration via intelligent quercetin delivery

Henigul osman,Xiaohui Tang,Dong Zhang,Bo Liu,Jie Gao,Xin Chen,Tao Jiang,Haobo Pan,Yingbo Wang

To address the dual challenges of controlled drug delivery and microenvironment modulation in repairing osteoporotic bone defects, we developed a multifunctional poly(l-lactic acid) (PLLA)-based composite fibrous scaffold (PLLA/PDA/ZIF-8@Qu). The scaffold was fabricated via electrospinning, followed by in situ polydopamine (PDA) polymerization to robustly immobilize ZIF-8 nanocarriers loaded with quercetin (Qu) on the fiber surface. The mussel-inspired PDA coating served as an adhesive interlayer between ZIF-8 and PLLA. Additionally, it provided near-infrared (NIR) responsiveness and surface functionalization capability. Under osteoporotic acidic conditions (pH 5.0–6.0), the scaffold exhibited pH-triggered release behavior, ZIF-8 degradation accelerated Zn 2+ release, and cumulative Qu release reached 90 %. Zn 2+ contributed to antibacterial activity, while the PDA coating enabled NIR-driven photothermal/photodynamic synergy, achieving 100 % inhibition against both E. coliand S. aureus. Quercetin (Qu) exerted antioxidant effects via the Nrf2/ARE pathway and promoted macrophage polarization toward the M2 phenotype, thereby ameliorating the local inflammatory microenvironment. In vitro , the scaffold enhanced osteogenic differentiation of bone marrow mesenchymal stem cells, as indicated by a 2.3-fold increase in alkaline phosphatase activity, a 1.85-fold increase in mineralized nodule formation, and upregulated Runx2 expression. In a rat femoral defect model, the scaffold group at 8 weeks post-implantation showed increased bone mineral density (BMD) from 0.454 to 0.935 g/cm 3 and trabecular number (Tb.N) from 0.694 to 0.923 mm −1 , with the defect largely filled by newly formed bone. Collectively, these results demonstrate that the PDA-enabled, ZIF-8/Qu-integrated PLLA scaffold couples pH-responsive release with antibacterial, anti-inflammatory, and pro-osteogenic functions, supporting its potential as a bone repair material responsive to pathological microenvironments.

CAS / MDL: 5970-45-6
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