JOURNAL OF MEMBRANE SCIENCE
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2026
·
IF 8.8
Hang Yang,Qiankun Sha,Yixuan Wang,Xiaohui Lu,Chang Ma,Na Han
Efficient separation of organic dyes from inorganic salts in high-salinity textile wastewater remains a major challenge for resource recovery. Although graphene oxide (GO) membranes show promise for ion-sieving applications, their practical use is hindered by interlayer swelling, pore compaction, and the inherent permeability–selectivity trade-off. Here, a synergistic interlayer-engineering strategy based on a “skeleton–filler” architecture is proposed using CNT/UiO-66-NH 2 to regulate the GO/substrate interface. In this architecture, carboxylated multi-walled carbon nanotube (MWCNT-COOH) scaffolds, together with metal–organic framework (MOF) particles, effectively mask the macroporous defects of the substrate and suppress sagging of the flexible GO nanosheets. Meanwhile, the hierarchical interlayer creates low-resistance transport pathways, thereby generating a gutter effect and reducing mass-transfer resistance. Consequently, the optimized GCU-27 membrane delivers a high water permeance of 105.14 L·m ‒2 ·h ‒1 ·bar ‒1 , together with a high Congo red rejection of 99.91% and a low MgCl 2 rejection of 3.60%. As a result, a high separation factor of 1071.11 is achieved. In addition, GCU-27 shows good antifouling performance ( = 88.16%) and stable separation performance during 100 h of continuous operation at 70 °C. This work provides an effective interfacial-engineering strategy and mechanistic insight for the rational design of high-performance GO-based membranes for dye/salt fractionation.
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LANGMUIR
·
2026
·
IF 4.4
Yue Qiu,Yingying Ling,Yahong Yuan,Tianli Yue,Fei Lyu
Patulin (PAT), a hazardous mycotoxin found in fruits and their products, poses significant health risks. While UiO-66-NH2 has been primarily explored as an adsorbent or carrier for mycotoxin removal, this study investigates its previously underexplored role as an oxidase-mimicking nanozyme for PAT degradation. UiO-66-NH2 achieved a maximum degradation efficiency of 84.01% within 48 h and 97.63% after 96 h. Mechanism studies revealed that the Zr–O cluster activates O2 to generate reactive oxygen species (·O2– and ·OH), which mediate the oxidative opening of the lactone and furan rings in PAT. The −NH2 enhances both PAT affinity and electron transfer of UiO-66. Three-dimensional fluorescence and LC-MS/MS analyses identified four degradation products (C7H7O5, C7H9O7, C4H5O5, and C3H5O3), enabling the proposal of a plausible degradation pathway. Applied to apple juice, UiO-66-NH2 removed 85.29% of PAT in 72 h, with a negligible impact on juice quality. This work offers an efficient nanozyme-based strategy for PAT detoxification in food applications.
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Journal of Energy Storage
·
2026
·
IF 10.7
Shang Wu,Qiyue Tong,Huize Zhang,Zhenyang Yu,Chenxu Zhu,Qiong Su,Hong Zhang,Guihua Li,Xiaojun Yang,Juzhen Kang,Quanlu Yang
NH 2 -UIO-66 has been regarded as a promising porous material owing to its high specific surface area and structural stability, although its limited conductivity restricts its application in supercapacitors. In this work, a NiCo 2 S 4 /NH 2 -UIO-66 nanoflower composite (NCS/NU) was synthesized via a vulcanization process with thioacetamide. Electrochemical measurements conducted in a three-electrode system revealed that the composite delivered a specific capacitance of 172.4 mAh g −1 at 1 A g −1 and maintained 82.1% of its initial capacitance after 5000 cycles at 5 A g −1 . Morphological characterization indicated that the nanoflower architecture was largely preserved after sulfurization. The in-situ formed NiCo 2 S 4 contributed to enhanced pseudocapacitance and induced surface wrinkling of the petals, which helped stabilize the composite structure supported by NH 2 -UIO-66. For the anode, S and N co-doped three-dimensional porous carbon (SNC) was prepared via a sol-gel method followed by stepwise high-temperature carbonization using ammonium persulfate as the activator. A hybrid supercapacitor was subsequently assembled with the NCS/NU as the positive electrode and SNC-700 as the negative electrode. The device delivered an energy density of 28.8 Wh kg −1 and retained 74.1% of its initial capacitance after 5000 charge-discharge cycles.
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Journal of Environmental Chemical Engineering
·
2023
·
IF 7.7
Huihu Wang,Hao Tu,Feng Chen,Huang Xu,Ziguan Zhang,Guode Chen,Chenhuinan Wei,Xing Xiang,Zhixiong Xie
Through a facile oil bath method, a novel highly dispersed NH 2 -MIL-101(Fe)/carboxylated g-C 3 N 4 (NM-101(Fe)/CCN) heterostructure was prepared using the chemical bonding between carboxyl groups and -NH 2 groups. Compared with the octahedral morphology of pure NM-101(Fe), the chemical bonding interaction promoted the heterogeneous nucleation and growth of NM-101(Fe) to form nanometer-sized granular morphology, which was homogeneously dispersed on CCN surface. Cr(Ⅵ) and ciprofloxacin (CIP) were selected as the typical pollutant models in micro-polluted water sources. The results showed that 10 %NM-101(Fe)/CCN heterostructure could remove 97 % of Cr(Ⅵ) in 60 min and 88 % of ciprofloxacin (CIP) in 120 min. In the dual pollutant system of Cr(Ⅵ) and CIP, Cr(Ⅵ) reduction and CIP degradation can promote each other, and the degradation efficiency of CIP reached 96 % within 120 min. The apparent rate constant of 10 %NM-101(Fe) /CCN heterostructure for Cr(Ⅵ) reduction was 4.30 and 9.67 times of that of NM-101(Fe) and CCN, respectively, which may be ascribed to the interface electric field and good interface bonding of heterojunction . The charges separation efficiency was significantly improved, which effectively enhanced the photocatalytic activity.
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Materials Today Chemistry
·
2023
·
IF 7.3
Wenlong Sheng,Fengwei Huang,Xianjun Lang
Metal–organic frameworks (MOFs) have received increasing attention for conducting miscellaneous photocatalytic reactions. Amorphous TiO 2 , despite the lack of visible light activity, can be a platform for integrating with a Ti-based MOF NH 2 -MIL-125(Ti) during hydrothermal process. Herein, amorphous TiO 2 microspheres are synthesized to enhance the activity of NH 2 -MIL-125(Ti) by integration. The morphology, porosity, and activity of NH 2 -MIL-125(Ti)/amorphous TiO 2 microspheres are systematically investigated by various methods. The photocatalyst NH 2 -MIL-125(Ti)/amorphous TiO 2 exhibits enhanced conversions, more than five times that of pristine NH 2 -MIL-125(Ti), for the selective oxidation of benzylamine. A series of optical and electrochemical characterizations are performed to clarify the mechanism for the photocatalytic selective oxidation of benzyl amines. Specifically, for NH 2 -MIL-125(Ti)/amorphous TiO 2 , visible light absorption is from NH 2 -MIL-125(Ti); and faster electron transfer to molecular oxygen is due to amorphous TiO 2 . This work shows that integrating MOFs with metal oxides can be crucial in enhancing visible light photocatalysis .
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JOURNAL OF COORDINATION CHEMISTRY
·
2023
·
IF 1.9
Yanbing Yin,Yang Liu,Zhou Wang,Yongming Feng,Bei Jiang
A ternary composite α-DMACoPc/UiO-66-NH2/TiO2 was synthesized by solvothermal method and characterized by X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FT-IR), scanning electron microscopy (SEM) and other means. The composite catalyst was applied to decompose methylene blue dye in visible light, and the degradation rate reached 93.4%. Compared with the monomer, the composite significantly enhanced the efficiency of the catalytic degradation due to the synergistic effect between composites. The transport speed of charge is accelerated and the recombination of hole-electron pairs is inhibited due to the larger specific surface area. A feasible scheme was provided for preparation of composite catalyst and photocatalytic degradation of dye.
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Nature Photonics
·
2023
·Vol. 17
·期 8
·694-701
·
IF 35
Mutailipu Miriding,Han Jian,Li Zhi,Li Fuming,Li Junjie,Zhang Fangfang,Long Xifa,Yang Zhihua,Pan Shilie
Phase-matching of light waves is a critical condition for maximizing the efficiency of nonlinear frequency conversion processes in nonlinear optical crystals; however, phase-matching, commonly achieved by tuning birefringence, is often difficult to achieve over a wide wavelength range. Here, full-wavelength phase-matching crystals that can avoid phase-mismatching across the entire optical transparency range are proposed. The anisotropic strength of bonding in the dimension of energy is confirmed theoretically to be the key to the full-wavelength phase-matching ability. We demonstrate that a crystal of guanidinium tetrafluoroborate (C(NH 2 ) 3 BF 4 ) can be phase-matched throughout its entire optical transparency range and is able to generate harmonic light as short as ~193.2 nm, which is close to its deep-ultraviolet cut-off edge. Importantly, this crystal is stable, cheap and efficient compared with commercially available nonlinear optical crystals for generation of 266 nm light. This work lays the foundation for finding a new class of crystals in which the phase-matching wavelength fully covers its optical transparency range, and also provides a high-performance crystal for generating light at 266 nm—the fourth-harmonic of a commercial 1,064 nm laser.
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TALANTA
·
2022
·
IF 6.556
Pengfei Zhao,Sisi Tang,Xiaodan Wu,Yu Chen,Kangling Tang,Jinli Fu,Huibin Lei,ZhaoXia Yang,Zhaohui Zhang
Development of method with micro-volume reagent usage and high selectivity for rapid determination of valuable disease-related biomarkers is of great importance for disease surveillance. Herein, a novel ratiometric fluorescence capillary imprinted sensor was developed for highly selective fluorescence determination of sialic acid (SA) based on luminescent metal-organic framework (UiO-66-NH 2 ). In this strategy, the imprinted pre-polymer with double emissions was sucked into the capillary to grow imprinted layer on the inner wall of the capillary. In presence of SA, the blue fluorescence (440 nm) served as fluorescence response signal was quenched due to the electron transfer mechanism between metal organic framework and SA while the red fluorescence (655 nm) served as the reference signal was remained. Within SA concentration linear range of 1.0 × 10 −7 –3.0 × 10 −4 M, the ratiometric fluorescence capillary imprinted sensor was applied to detect SA in human serum and saliva samples successfully with a detection limit of 2.5 × 10 −8 M. A sensitive and selective fluorescence method with micro-volume sample consumption (15 μl) for determination of SA in practical samples was established.
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ANALYST
·
2022
·Vol. 147
·期 24
·5655-5662
·
IF 5.227
Ying Zhou,Ruichun Li,Guomei Zhang,Yan Zhang,Caihong Zhang,Shaomin Shuang
Metal–organic frameworks (MOFs) have emerged as interesting nanomaterials owing to their large surface area, high porosity, tunable pore architecture and easy functionalization. However, an inferior electrical conductivity hinders their application in electrochemical sensing. In this paper, gold–palladium alloy/UiO-66-NH2/graphene (AuPd/UiO-66-NH2/GN) composites were synthesized by loading alloys on the surfaces of MOFs and then attaching them to the graphene surface. The addition of metal nanoparticles and graphene enhanced the electron transfer ability of MOFs. Then, composites were used to modify a glassy carbon electrode (GCE) to construct a sensitive dopamine (DA) electrochemical sensor. The developed sensor manifested two linear relationships in lower concentration ranges and in higher concentration ranges with a 0.21 × 10−6 mol L−1 low detection limit (3σ/k) under optimal conditions. The results certified that the constructed sensor had high selectivity, excellent reproducibility and good stability, and had been used successfully for DA detection in actual human serum samples.
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Environmental Science-Nano
·
2022
·Vol. 9
·期 8
·3081-3093
·
IF 9.473
Yuqi Wan,Huaizhi Yang,Qigao Shang,Qingrong Cheng,Hong Zhou,Zhiquan Pan
A novel metal–organic framework@covalent organic framework (MOF@COF) heterojunction was synthesized based on post-synthetic covalent modification. In the present work, aldehyde-modified MOFs (NH2–MIL-101(Fe)) were covalently bonded with covalent organic frameworks (Schiff base network-1, SNW-1) forming the NH2–MIL-101(Fe)@SNW-1 (MS-x) heterojunction by using this strategy. The MS-x heterojunction showed excellent photodegradation ability for pollutants and photocatalytic hydrogen production under simulated sunlight. The superior photocatalytic performance of the MS-x heterojunction can be attributed to the formation of –CN– bonds between NH2–MIL-101(Fe) and SNW-1, which enhances the charge separation efficiency and improves the stability of the photocatalyst. It is worth mentioning that SNW-1 on the surface of the catalyst had a hollow structure which can promote the photoelectric charge migration. Furthermore, the results verified that the matched band structure of NH2–MIL-101(Fe) and SNW-1 could induce a type II heterojunction, which could well explain the improved photocatalytic performance of the photocatalytic system. This work not only provides a new idea to construct highly efficient and stable MOF@COF heterojunctions but also broadens the applications of COF-based materials.
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NEW JOURNAL OF CHEMISTRY
·
2022
·Vol. 46
·期 17
·8203-8214
·
IF 3.925
Lingli Zhang,Han Tao,Chun Ji,Qiaoling Wu,Xiao Wang,Yuangeng Wu
As an alternative to bisphenol A (BPA), bisphenol S (BPS) is widely used in many consumer goods and industrial products. However, BPS has similar genotoxic, reproductive and endocrine disrupting effects to BPA and can enter the body through the food chain or by dermal absorption to endanger human health. This paper presents a rapid and direct electrochemical sensing technique for ultra-trace BPS determination on the basis of the signal amplification of the 1T phase & 2H phase hybrid MoS2 nanosheets (1T&2H-MoS2) and amino-functionalized carbon nanotube (CNTs-NH2) composites. The cooperative electrocatalytic effect and high-electrically active surface area of 1T&2H-MoS2/CNTs-NH2 composites not only facilitated the electron transfer between BPS and the electrode, but also promoted the adsorption of BPS on the electrode. Hence, the 1T&2H-MoS2/CNTs-NH2 modified electrode exhibited excellent electrocatalytic activity with a lower oxidation potential and higher peak current for BPS. Under the optimized conditions, the peak current response of BPS showed a good dose-dependent relationship with its concentration in the range of 0.02–1.0 μM and 1.0–70.0 μM, while the detection limit was as low as 8.6 nM. The proposed method was used to determine BPS in the mineral water bottle and orange juice samples with satisfactory spiked recoveries between 92.31% and 104.20%, demonstrating its reliability and practicality in real sample analysis. Furthermore, the sensing method has the characteristics of facile electrode fabrication, fast response (<4 min) and good reproducibility.
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CHIRALITY
·
2022
·Vol. 34
·期 3
·462-472
·
IF 2.183
Zhen Wang,Wan-Qi Xiong,Zhi-Feng Huang,Gai-Zhao Qin,Min Zi,Li-Ming Yuan
Chiral covalent organic framework materials have many excellent properties, which have received much attention in the field of separation. Synthesized the covalent organic framework COF-TpBD (NH 2 ) 2 modified, respectively, by L-valine trifluoroacetyl derivative, L-hydroxyproline, and (1S)-(+)-10-camphorsulfonyl chloride, three capillary columns of chiral covalent organic framework materials were obtained for gas chromatography. Those columns are able to separate some chiral compounds, positional isomers, n-alkanes, n-alcohols, aromatic hydrocarbon mixture, and Grob's reagents. They are complementary to other chiral capillary columns and are possible for potential applications.
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