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Polymers · 2026 ·Vol. 18 ·期 14 ·1699 · IF 5.8

Fabrication of Multifunctional Films Incorporating Purple Sweet Potato Anthocyanins and ZIF-8-NH2@Rt for Monitoring and Preservation of Pork Freshness

Yangjie Huang,Haixia Wang,Yiyuan Zhang,Yuhang Liu

Natural antioxidants are limited in food packaging due to poor stability and compatibility. A multifunctional film was successfully prepared via the incorporation of functional fillers into a guar gum/polyvinyl alcohol (GP) matrix. ZIF-8 was amino-functionalized to enhance rutin (Rt) loading, and the resulting ZIF-8-NH2@Rt was combined with purple sweet potato anthocyanins (PSPA) to fabricate a composite film for pork freshness monitoring. Compared with neat GP, the ZIF-8-NH2@Rt/PSPA/GP film showed a 30.6% increase in tensile strength and an elongation at break of 36.6%. The composite film also imparted exceptional UV-blocking capabilities, with light transmittance plummeting to 3.22% in the UVA region, 0.40% in the UVB region, and 47.53% within the visible light spectrum. The films displayed significant antioxidant properties, with DPPH and ABTS scavenging activities recorded at 73.27% and 67.64%, respectively. During pork storage, the film exhibited stable color changes. The G/R values corresponding to the limit of edibility were determined to be 0.78 and 0.67 for storage at 25 °C and 4 °C, respectively. The film was reusable for four cycles and extended the shelf life of pork by at least one day. These findings highlight the film’s considerable promise in the realm of smart food packaging and dynamic freshness tracing.

CAS / MDL: 9000-30-0
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CHEMISTRY-A EUROPEAN JOURNAL · 2026 · IF 3.6

In-situ Growth of UiO-66-NH2 on Carboxymethylated Cellulose Beads for Enhanced Low Concentration Fluoride Ions Removal From Aqueous Solution

Weiya Niu,Yongjian Wang,Sucheng Liu,Yizhe Wang,Zhengchao Liang,Yu Zhang,Renliang Lyu,Xiaogang Luo

The development of high-capacity and selective adsorbents for fluoride (F − ) removal is hindered by its inherent characteristics, including its small ionic radius, high charge density, strong hydration ability, high mobility and solubility, as well as the weak diffusion driving force at low concentrations. In this study, a novel composite adsorbent was prepared by loading UiO-66-NH 2 onto carboxymethylated cellulose beads (UiO-66-NH 2 @CMCBs) via an in-situ generation strategy for efficient adsorption and recovery of F − . The highly porous structure and abundant surface carboxyl groups of CMCBs provide favorable coordination sites, promoting the growth of UiO-66-NH 2 . Under environmental conditions (25°C, pH 7.4), UiO-66-NH 2 @CMCBs completely remove F − from aqueous solutions with an initial concentration of 10.0 mg L −1 . Furthermore, UiO-66-NH 2 @CMCBs demonstrated excellent column adsorption performance and outstanding reusability, maintaining a removal efficiency exceeding 80% after 5 cycles. These results highlight the potential of UiO-66-NH 2 @CMCBs as an efficient and recyclable adsorbent for the practical treatment of fluoride-contaminated water. Graphical

CAS / MDL: 10312-55-7 3926-62-3
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LANGMUIR · 2026 · IF 4.4

Carbon Dots-Mediated Z-Scheme Heterojunction of UiO-66-NH2/BiOCl for Enhanced Visible-Light-Driven Degradation of Antibiotics and Dyes

Xinhua He,Zijie Xia,Linlin Wang,Tianchen Shen,Wenqi Tan,Jianmin Shen,Linying Yuan,Zheng Jiao

The ubiquitous accumulation of antibiotics and synthetic dyes in aquatic environments has emerged as a critical threat to the ecological integrity and human health. Visible-light-driven photocatalysis represents a sustainable strategy for decontaminating such pollutants; yet, its practical efficacy is often hampered by narrow light-harvesting ranges and rapid photogenerated carrier recombination. Herein, a ternary photocatalyst, namely, CDs/UiO-66-NH2/BiOCl (CUCl), was rationally constructed by integrating carbon dots (CDs) into a UiO-66-NH2/BiOCl Z-scheme heterojunction. Serving as an efficient electron reservoir, the introduced CDs not only significantly extended the visible-light absorption range but also effectively suppressed carrier recombination. Under visible-light irradiation, the optimized CUCl catalyst achieved remarkable degradation efficiencies of 87.2% and 98.8% for tetracycline and rhodamine B, respectively, outperforming the binary UiO-66-NH2/BiOCl heterojunction and pristine BiOCl. Radical trapping experiments and photocatalytic mechanism investigations revealed that photogenerated holes (h+) and superoxide radicals (·O2–) were the dominant active species responsible for pollutant degradation. Moreover, the CUCl catalyst exhibited excellent structural stability and reusability, retaining more than 85% of its initial catalytic activity after four consecutive reuse cycles. This work provides a novel and viable strategy for fabricating high-efficiency, stable environmental photocatalysts via the synergistic integration of Z-scheme heterojunctions and carbon dot functionalization.

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Journal of Environmental Chemical Engineering · 2026 ·Vol. 14 ·期 2 ·121676 · IF 7.5

Synergistic IL grafting and NH2-ZIF-8 doping enable PVDF composite membranes with enhanced separation, antifouling, and piezo-photocatalytic degradation functions

Xiaonan Hao,Ying Xue,Yue Wu,Shulin Sun

The inherent hydrophobicity of polyvinylidene fluoride (PVDF) separation membranes severely limits their flux and anti-fouling performance, and traditional membrane materials struggle to simultaneously achieve efficient separation and degradation of pollutants. This study innovatively proposes a synergistic modification strategy combining Chlorinated 1-butyl-3-vinylimidazole (IL) grafting with amino-functionalized zeolitic imidazolate framework-8 (NH 2 -ZIF-8) doping. This approach constructs a multifunctional composite membrane integrating efficient separation, adsorption, and piezo-photocatalytic degradation. The prepared PVDF-g-IL/NH 2 -ZIF-8 membrane demonstrates outstanding overall performance. Under combined ultrasound and ultraviolet excitation, it achieves a methylene blue degradation efficiency of 80.5 %, showcasing its capability for in-situ pollutant degradation during the separation process. Furthermore, the membrane exhibits a pure water flux as high as 685.6 L m −2 h −1 , which is approximately seven times that of the pristine PVDF membrane. It also maintains dye rejection rates exceeding 93 % for various dyes, and possesses a high adsorption capacity (>7.0 mg/g) along with excellent cycling stability due to the flux recovery rate above 80 %. This study provides new insights for developing water treatment membranes combined efficient separation with in situ degradation functionality.

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Food Analytical Methods · 2026 ·Vol. 19 ·期 9 ·248 · IF 3

Preparation and Application of Microporous Core–shell ZIF-8@UiO-66-NH2 Composite As High-performance Stationary Phase in Capillary Electrochromatography

Qin Shili,Zhao Dongsheng,Jin Fenglong,Qin Yuting,Liang Xinyu,Liu Jingwen,Chu Hongtao,Gao Lidi,Zhao Ming

In this study, the octahedral core–shell ZIF-8@UiO-66-NH 2 composite, exhibiting high crystallinity, microporous structural properties and multifunctional groups, was synthesized, characterized, and applied for the first time as stationary phase in capillary electrochromatography. The baseline separation of four groups containing 14 analytes was achieved within 11.6 min, with resolution of at least 1.51. Compared to the individual components of ZIF-8 and UiO-66-NH 2 used as chromatographic stationary phase, the bonded capillary column based on ZIF-8@UiO-66-NH 2 exhibited the improvement in resolution and column efficiency (theoretical plate numbers) ranging from 68.14 to 918.75% and from 3.92 to 398.31%, respectively, and sample loading capacity increased by ≥ 26.8%. Furthermore, an accurate, rapid, and reliable electrochromatography method was developed for the qualitative and quantitative analysis of thiamphenicol and florfenicol in pork meat. The limits of detection and quantification for thiamphenicol were 0.34 μg/mL and 1.75 μg/mL, and for florfenicol, 1.00 μg/mL and 5.82 μg/mL, with sample recoveries in the range of 96.00 to 108.00% and the standard deviations less than 4.59%. This work not only confirmed the potential of MOF@MOF composite as high-performance stationary phases but also broadened the electrochromatography application in food inspection. Graphical The alternative text for this image may have been generated using AI.

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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2026 · IF 4.4

Fabrication of NH2-MIL-101(Fe)/few-layer Ti3C2 Schottky heterojunctions to boost charge separation for enhanced photocatalytic Cr(VI) elimination

Bingkun Liu,Juncheng Guo,Ziyang Liang,Yuhan Yang,Beibei Liu,Bing Han,Yonghui Zhang

NH 2 -MIL-101(Fe)/few-layer Ti 3 C 2 Schottky heterojunctions are constructed. • NH 2 -MIL-101(Fe)/Ti 3 C 2 composite shows higher photocatalytic activity for Cr(VI) removal. • The Schottky heterojunctions boost the separation of photogenerated charges. • The photogenerated electrons and •O 2 − dominate the Cr(VI) reduction process. The limited charge transfer efficiency of single-component semiconductor photocatalysts remains a critical bottleneck restricting the photocatalytic elimination of harmful pollutants. Here, NH 2 -MIL-101(Fe) nanoparticles are anchored onto few-layer Ti 3 C 2 nanosheets via electrostatic self-assembly to construct NH₂-MIL-101(Fe)/Ti 3 C 2 heterostructure. The few-layered 2D Ti 3 C 2 supplies abundant adsorption and catalytic active sites. Furthermore, benefiting from the Schottky junction and the superior conductive feature of Ti 3 C 2 MXene, the separation and transport of photoinduced carriers are remarkably promoted in the NH 2 -MIL-101(Fe)/Ti 3 C 2 . Accordingly, the optimized NH 2 -MIL-101(Fe)/Ti 3 C 2 –10% sample can remove 95.7% of Cr(VI) after 150 min of visible-light irradiation and still exhibits favorable reusability after three cycles. The electrons and •O 2 − are confirmed as the primary active species driving Cr(VI) reduction. Combined with comprehensive characterizations, a plausible photocatalytic mechanism of Cr(VI) reduction is put forward. This work offers fundamental guidance for developing MXene-based Schottky heterostructures toward improved photocatalytic activity.

CAS / MDL: 10025-77-1 140-22-7
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Science China-Materials · 2021 ·Vol. 64 ·期 8 ·2008-2016 · IF 8.273

[C(NH2)3]3PO4·2H2O: A new metal-free ultraviolet nonlinear optical phosphate with large birefringence and second-harmonic generation response

Wen Xin,Lin Chensheng,Luo Min,Fan Huixin,Chen Kaichuang,Ye Ning

[PO 4 ] 3− possesses small microscopic second-order susceptibility and polarizability anisotropy, which inherently result in weak second-harmonic generation (SHG) and small birefringence. Herein, a new noncentrosymmetric phosphate, [C(NH 2 ) 3 ] 3 PO 4 ·2H 2 O, was successfully designed and synthesized by a solution evaporation method. [C(NH 2 ) 3 ] 3 PO 4 ·2H 2 O without metal ions is composed of planar conjugated guanidine cations and PO 4 tetrahedrons, which are connected by hydrogen bonds, forming a three-dimensional network. Physical property measurements indicate that the title compound displays an SHG response of 1.5 × KH 2 PO 4 (KDP) and a larger birefringence (0.055@546.1 nm) compared with most reported ultraviolet nonlinear optical phosphates. Furthermore, first-principles calculations reveal that the π-conjugated planar [C(NH 2 ) 3 ] + cations and [PO 4 ] 3− groups are responsible for its excellent linear and NLO properties.

研究领域: 材料科学 · 光学工程 · 无机化学 · 晶体工程 · 非线性光学
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ELECTROCHIMICA ACTA · 2026 · IF 5.6

DFT-Guided Rational Design of a UiO-66-NH2/MFC Composite Separator with Hierarchical Pores for Modulating Interfacial Lithium-ion Transport

Yuan Jin,Yanhong Zhang,Fuzhi Li,Guangli Li

To address microfibrillated cellulose (MFC) separator shortcomings in lithium-ion flux homogenization and dendrite growth due to uneven ion distribution, this study developed a UiO-66-MFC composite separator with 20-30% loading. The hierarchical pores (0.8-1.2 nm micropores and 2-50 nm mesopores) enable selective Li + screening and rapid transport, while MFC's hydroxyl groups form hydrogen bonds with amino groups of UiO-66-NH 2 , enhancing mechanical strength to 16 MPa at a 20% loading. Density functional theory (DFT) calculations further reveal a strong interaction between -NH 2 and PF 6 - , with a binding energy reaching -8.622 keV. This interaction effectively restricts the migration of PF 6 - , promotes the desolvation process of lithium salts, accelerates Li⁺ transport, and fosters more uniform lithium deposition behavior. The electrochemical test results indicate that the 20% UiO-66-NH 2 /MFC separator demonstrates the most favorable overall performance. After cycling for 1000 h at a current density of 1 mA cm -2 , the overpotential of the Li/Li symmetrical battery remains stable at ± 0.10 V, suggesting effective inhibition of lithium dendrite growth. When paired with the LiFePO 4 cathode, the battery exhibits a capacity retention rate exceeding 90% after 100 cycles, while the coulombic efficiency approaches 100%. This study significantly improves the ion conduction and interface stability of the separator by optimizing the MOF ratio, thereby offering a novel strategy for the material design of high-safety and long-life lithium-ion batteries. This MOF-incorporated MFC strategy significantly enhances separator ion conduction and stability, offering a novel approach for safe, long-life lithium-ion batteries.

CAS / MDL: 64-17-5 67-63-0 75-65-0
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JOURNAL OF CHROMATOGRAPHY A · 2026 · IF 4

Selective and sensitive determination of chlorophenol disinfection by-products in fish by defective MIL-101(Fe)-NH2 membrane SPE-HPLC-UV

Xueyun Wei,Lanrui Yang,Zhuomin Zhang,Gongke Li

Trace disinfection by-products (DBPs) in aquatic products may have serious impact on human health via direct or indirect consumption. However, the accurate and sensitive quantification of trace chlorophenol DBPs in complex aquatic products still remains a great challenge. In this work, the defective MIL-101(Fe)-NH 2 enrichment medium was prepared for developing a selective membrane solid phase extraction (M-SPE) technology for quantifying trace chlorophenol DBPs in fish, coupled with high performance liquid chromatography-ultraviolet-visible spectroscopy (HPLC-UV). The established analytical method showed good selectivity, sensitivity and accuracy, achieving the limits of detection from 0.03 to 0.15 ng/mL and the recovery from 80.0% to 117%, achieving sensitivity comparable to that of HPLC-mass spectrometry (MS)-based methods. The validated method was successfully applied to quantify chlorophenol DBPs in grass carp and crucian carp, offering a selective and sensitive alternative for monitoring chlorophenol DBPs in fish, with practical advantages for routine analysis via compatibility with widely available HPLC-UV.

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MICROCHEMICAL JOURNAL · 2020 · IF 3.594

Electrochemical sensing and simultaneous determination of guanine and adenine based on covalent organic frameworks/NH2-rG/MoS2 modified glassy carbon electrode

Xin Zhao,Hao Guo,Rui Xue,Mingyue Wang,Qixia Guan,Tian Fan,Wenhu Yang,Wu Yang

Alteration in the concentrations of guanine (G) and adenine (A) leads to various abnormalities in the metabolic process which causes various diseases. Therefore, it still remains a challenge to establish an accurate, simple and accurate method for simultaneous detection of guanine and adenine. In this paper, using covalent organic frameworks (COFs) as a carrier and the amino functionalized reduced graphene oxide as charge transfer accelerator, layer molybdenum disulfide (MoS 2 ) nanosheets are deposited on glassy carbon electrode (GCE) by simple physical stacking to fabricate a dual-signal amplification biosensor for simultaneous detection of adenine and guanine. Under optimized conditions, the electrochemical behaviors of guanine and adenine on the COFS/NH 2 -rG/MoS 2 modified electrode were studied by cyclic voltammetry and differential pulse voltammetry. The sensor performs well in determining G and A at the same time with wide linear ranges of 0.5–150.0 μM and 1.0–280 μM and low detection limits of 0.51 μM(S/N = 3) and 0.44 μM(S/N = 3), respectively. The sensor was successfully used to assay G and A in thermally denatured herring sperm DNA, and the G/A ratio was calculated to be 0.79. The biosensor has the advantages of simplicity, speed, high sensitivity, good reproducibility, and long-term stability.

研究领域: 电化学 · 生物传感 · 纳米材料 · 分析化学 · 生物化学
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CRYSTAL GROWTH & DESIGN · 2021 · IF 4.076

Te(CS(NH2)2)4SO4·2H2O: A Three-in-One Semiorganic Nonlinear Optical Crystal with an Unusual Quadrilateral (TeS4)6– Chromophore

Xiaoya Weng,Chensheng Lin,Guang Peng,Huixin Fan,Xin Zhao,Kaichuang Chen,Min Luo,Ning Ye

The first tellurium(II) thiourea sulfate semiorganic nonlinear optical (NLO) material, Te(CS(NH2)2)4SO4·2H2O, was successfully obtained using the slow evaporation technique. The structure of this metal-free crystal featured three types of NLO-active units, namely CS(NH2)2, (SO4)2–, and (TeS4)6–, which synergistically contributed to its moderate second harmonic generation response (2.4 × KDP@1064 nm) and large birefringence (0.210@546.1 nm). Remarkably, this is the first example in which the quadrangular (TeS4)6– groups significantly contributed to the SHG effect and birefringence, and the first principles calculations revealed its special mechanism of NLO activity. These findings highlighted the exploration of semiorganic NLO materials and provide new opportunities for the discovery of new NLO crystals.

研究领域: 晶体学 · 材料科学
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ChemNanoMat · 2023 ·Vol. 9 ·期 5 ·e202300051 · IF 3.8

Adsorption-Induced In-Situ Construction of TiO2 Hollow Sphere/UiO-66-NH2 Heterostructures with Boosted Photocatalytic Activity toward Cr(VI) Reduction

Qiankun Xu,Yaru Li,Wen Ji,Jun Mei,Xianbiao Wang

Graphical TiO 2 hollow sphere/UiO-66-NH 2 heterostructures were successfully synthesized by an adsorption-induced in-situ solvothermal growth strategy. The integration of TiO 2 and UiO-66-NH 2 could construct a type-II heterojunction to broaden the absorption range of light and suppress the recombination of photoproduced electrons and holes, thus boosting the photoreduction activity toward Cr(VI) of TiO 2 /UiO-66-NH 2 . Water contamination caused by highly toxic Cr(VI) should be resolved imminently with a more efficient photocatalytic approach. The interaction between photocatalyst heterostructure is critical for charge separation which largely affects the photocatalytic efficiency. Herein, TiO 2 hollow sphere/UiO-66-NH 2 (TiO 2 /UiO-66-NH 2 ) heterostructures were successfully synthesized by an adsorption-induced in-situ solvothermal growth strategy. The UiO-66-NH 2 particles were well dispersed on TiO 2 hollow spheres by solvothermal treatment of Zr 4+ adsorbed TiO 2 hollow spheres with NH 2 -BDC ligand. The photocatalytic activities of TiO 2 /UiO-66-NH 2 heterostructures were investigated by reduction of Cr(VI) with visible light irradiation. With the introduction of UiO-66-NH 2 , the reduction efficiency toward Cr(VI) by TiO 2 /UiO-66-NH 2 heterostructures reached 89% after 180 min of irradiation, which is much higher than those of TiO 2 hollow spheres (10%) and UiO-66-NH 2 crystals (29%). Moreover, the TiO 2 /UiO-66-NH 2 heterostructures display good regeneration ability and can still maintain 70% of Cr(VI) removal ability after four cycles. The integration of TiO 2 and UiO-66-NH 2 could construct a type-II heterojunction to broaden the absorption range of light and suppress the recombination of photoproduced electrons and holes. As a result, such unique composite structure significantly enhance the photocatalytic performance towards Cr(VI) reduction. This work not only inspires a new approach for in-situ solvothermal synthesis of semiconductor@MOFs composites, but provides a novel photocatalyst for highly efficient removal of Cr(VI) from wastewater.

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