CHINESE JOURNAL OF CHEMICAL ENGINEERING
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2018
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IF 1.712
Na Zhou,Yan Du,Chunyu Wang,Rizhi Chen
The state-of-the-art approaches for adjusting the structural characteristics of porous carbons are the after-treatments, which are complicated and time consuming. In this work, a facile approach was developed, i.e. , controlling the initial oxygen concentration in-situ during the direct carbonization of zeolitic imidazole framework-8 (ZIF-8), to adjust the pore structure and prepare hierarchically porous carbons. The introduction of oxygen can significantly affect the crystalline and pore structures of porous carbons, and promote the pore widening and the formation of mesopores . An appropriate initial oxygen concentration can notably enhance the surface area and mesopore volume of porous carbon, and then improve the adsorption capacity toward methylene blue (MB) dye from water by 3.4 times. The developed approach is more efficient at lower carbonization temperature. Moreover, the introduction of oxygen can increase the ratio of HO C O groups on the carbon surface, leading to enhanced interaction with MB molecules and higher adsorption capacity toward MB. The as-prepared porous carbons exhibit superior adsorption capacities toward MB dye as compared to the reported ZIF-8 derived carbons. These findings would aid the development of porous carbon materials with high performance.
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MICROCHEMICAL JOURNAL
·
2024
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IF 4.9
Yuanqian Xiong,Xiaoyu Gao,Yu Wang,Xiangrui Deng,Chunhong Xiong,Jinsheng Zhang,Qianhui Gu,Ganhui Huang
Norfloxacin (NOR) is now extensively used for the treatment of human and animal diseases. Unfortunately, large accumulations of NOR will pose a significant threat to the human body. Thus, it is urgent to develop a rapid and sensitive detection technique for the trace determination of NOR. In this study, an electrochemical molecular imprinting sensor with great properties was fabricated for the determination of NOR in milk and environmental water. The incorporation of bovine serum proteins produced a hybrid recognition interface consisting of molecularly imprinted polymers and peptides that provided good recognition properties for norfloxacin. The Fe 3 O 4 @ZIF-8 was distributed orderly on the electrode after the embedding of the magnets inside the electrode, then the BSA was coated on the electrode with the electrodeposited AuNPs through Au-S bonding. The sensor constructed in this study achieved ultra-sensitive detection of norfloxacin with an effective area of 0.08433 cm 2 , a limit of detection (LOD) of 0.108 pmol·L −1 , and a wide linear range (1 ∼ 100, 100 ∼ 1000 and 1000 ∼ 8000 pmol·L −1 ). The prepared sensors exhibited satisfactory performance in the detection of milk and environmental water, with acceptable recoveries ranging from 96.24 % to 104.88 %, and the relative standard deviation (RSD) was no more than 4.84 %.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2025
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IF 9
Yunxiang Bai,Xinxue Qiu,Deqiang Chen,Junwei Zheng,Liangliang Dong,Chunfang Zhang
Magnetic mixed matrix membranes (MMMs) show great potential for enhancing O 2 /N 2 separation efficiency by leveraging the inherent magnetic property differences between O 2 (paramagnetic) and N 2 (diamagnetic). However, one of the major challenges is the establishment and precise control of magnetic channels between magnetic fillers and polymer matrix. To address this issue, herein, ZIF-8 wrapped Fe 3 O 4 nanoparticles (Fe 3 O 4 @ZIF-8) were synthesized using a step-by-step assembly method, and then integrated into polymer of intrinsic microporosity (PIM-1) matrix to develop MMMs with well-defined magnetic channels for O 2 /N 2 separation. In comparison with Fe 3 O 4 , Fe 3 O 4 @ZIF-8 nanoparticles exhibited significantly enhanced compatibility with the polymer matrix, thereby facilitating uniform dispersion and improving interfacial adhesion. Gas permeation experiments revealed that the magnetic PIM-1/Fe 3 O 4 @ZIF-8 MMMs demonstrated enhanced O 2 /N 2 separation performance due to the combined effects of magnetic responsiveness and the presence of ZIF-8 magnetic channels. Under a magnetic field strength of 56mT, the magnetic MMM with a 4 wt% loading of Fe 3 O 4 @ZIF-8 exhibited optimal O 2 /N 2 separation performance with O 2 permeability of 710 Barrer and O 2 /N 2 selectivity of 3.64. These values represented a significant improvement of 42% and 24%, respectively, compared to pure PIM-1 membrane. Moreover, the simultaneous improvement of permeability and selectivity enabled the achievement of Robeson’s 2008 upper bound for O 2 /N 2 separation, underscoring the great potential of Fe 3 O 4 @ZIF-8 nanoparticles for designing magnetic MMMs with favorable structural attributes and exceptional separation efficiency.
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Polymers
·
2024
·Vol. 16
·期 23
·3351
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IF 4.7
Ya Chen,Xueyong Qiao,Guoran Sun,Zhonghui Han,Lei Lv,Xiaolei Zhao,Jinxing He
The development of fluorescent sensors with high sensitivity and fast response times is attracting the interest of more and more researchers. Herein, dual-emission ratiometric molecularly imprinted fluorescent encoded microspheres were fabricated and applied for the fast detection of norfloxacin. Core–shell-structured imprinted polymers with ZIF-8 as the supporting core were obtained first and two quantum dots with green and red emission provided the fluorescent signal. The introduction of the optical encoding technique greatly simplified the preparation process. After the addition of NOR, the green intensity at 525 nm remained constant and the fluorescent intensity at 625 nm decreased significantly because of the inner filter effect. Under the optimum detection conditions, a good linear correlation ranged from 5 μg L−1to 500 μg L−1, and the spiked recoveries of the method were 89.76%–106.94%. The detection limit for chicken, pork, fish, and milk samples was established at 2 μg L−1. More importantly, the established sensor provided a faster mass transfer rate, and the detection process took only 15 min, indicating great potential as an alternative for the fast detection of NOR in food samples.
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PubMed
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SEPARATION AND PURIFICATION TECHNOLOGY
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2024
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IF 8.1
Zeming Qiu,Feiyu Gao,Yuhan Zhang,Jinzhou Li,Yang You,Xuewei Lv,Jie Dang
Biomass adsorbents possess significant potential for both metal recovery from industrial leaching solutions and wastewater treatment. However, standalone biomass materials suffer from the drawback of low adsorption capacity. In this study, by the combination of metal–organic frameworks (MOFs) with organic biomaterials, a novel aerogel of aminated ZIF-8 composite cellulose (CPEZN) was developed for molybdenum ions adsorption, and the incorporation of aminated ZIF-8 improved the availability of reactive groups. The unique aerogel structure effectively prevented the accumulation of MOFs, thereby increasing the specific surface area and improving the exposure of active site. In addition, the positively charged surface of CPEZN effectively adsorbed molybdenum ions. Experimental results showed that the introduction of ZIF-8-NH 2 improved the adsorption performance of the composites. The adsorption of Mo(VI) followed the Langmuir adsorption isotherm model, and its adsorption rate followed the pseudo-second-order model. The adsorbent exhibited a maximum Mo(VI) adsorption capacity of 872.39 mg/g at pH = 3, and a removal rate of more than 80 % in mixed coexisting ion solutions. Moreover, the adsorbent demonstrated good stability, with a removal rate of above 80 % after 5 cycles of adsorption. Comprehensive characterizations revealed that the adsorption mechanism of Mo(VI) on CPEZN was a synergistic effect of chemisorption, electrostatic interaction, redox, and complex ligand processes. The simulated industrial wastewater adsorption experiment showed that the prepared adsorbent had good removal ability for molybdenum ions. This study not only provides a reference for the design and preparation of MOF and biomass-based composite adsorbent materials, particularly in terms of understanding the adsorption mechanism and designing high-capacity functional groups, but also provides a theoretical basis for its practical application.
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ACS Applied Materials & Interfaces
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2016
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IF 7.145
Juan Yang,Huili Ye,Faqiong Zhao,Baizhao Zeng
A novel core–shell heterostructure of CuxO nanoparticles@zeolitic imidazolate framework (CuxO NPs@ZIF-8) was successfully prepared through facile pyrolysis of a nanocrystalline copper-based metal–organic framework [nHKUST-1, i.e., Cu3(BTC)2 (BTC = 1,3,5-benzene-tricarboxylate)]@ZIF-8, based on the different thermal stability of the two metal–organic frameworks (MOFs). The small CuxO NPs derived from nHKUST-1 were uniformly dispersed inside the host material and provided active sites, while ZIF-8 kept the original structure as the molecular sieving shell. Owing to the proper pore shape and pore size of ZIF-8, H2O2 could diffuse through the shell, but bigger molecules could not pass. Thus, the composite material exhibited high selectivity when it was used to construct a H2O2 sensor. In addition, the sensor showed an extended linear detection range (from 1.5 to 21442 μM), low detection limit (0.15 μM), and high sensitivity, due to the good electrocatalysis of CuxO NPs and the synergistic effect of the core–shell structure.
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APPLIED CATALYSIS B-ENVIRONMENTAL
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2016
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IF 8.328
Jianxin Liu,Rui Li,Yingyuan Hu,Tan Li,Zehui Jia,Yunfang Wang,Yawen Wang,Xiaochao Zhang,Caimei Fan
An Ag@AgCl/Ag nanofilm/ZIF-8 composite photocatalyst was successfully constructed for the first time by loading Ag@AgCl and Ag nanofilm on the surface of ZIF-8 simultaneously via a simple deposition-photoreduction method. The formed Ag nanofilm was harnessed as a mediator to transfer photo-induced electrons from the plasmonic Ag@AgCl nanostructure to ZIF-8 for enhancing the photocatalytic reaction rate with visible light. The photocatalytic activity was evaluated by photocatalytic degradation of methylene blue (MB) under visible light irradiation. The first-order kinetic constant of MB degradation over Ag@AgCl/Ag nanofilm/ZIF-8 (14.762 h −1 ) was nearly 2 times of Ag@AgCl/ZIF-8 (7.932 h −1 ). The electrochemical impedance spectra, photoelectric conversion spectra and ESR DMPO-O 2 − species spectra revealed that AFZ had a lower resistance, higher photocurrent density and more generation of superoxide radical than those of AZ, meaning that the extended interface between Ag nanofilm and ZIF-8 could promote the quick electrons transfer and electron-hole pairs separation. This work provides a new type electrons transfer mediator in fabrication of efficient plasmonic photocatalysts.
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CHEMICAL ENGINEERING JOURNAL
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2024
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IF 13.3
Ye Tian,Wenlong Xie,Zihao Yang,Zhendong Yu,Renjie Huang,Lin Luo,Miao Zuo,Zheng Li,Lu Lin,Xianhai Zeng
Selective ring-opening hydrogenolysis of furfural (FF) to 1,5 pentanediol (1,5-PeD) is crucial for biomass valorization. However, achieving accurate bond-breaking is challenging. Herein, we report a facile method to synthesize layered double hydroxide nanoflake (ZnCo-LDH) mediated via Co 2+ etching ZIF-8 with NaBH 4 in water at ambient temperature. The structure, morphology, and chemical properties of synthesis catalysts with different concentrations of Co 2+ were characterized. The results indicated a partial ZIF-8 structure in ZnCo-LDH, with increased Co 2+ concentrations leading to catalyst agglomeration. Furthermore, the constitutive relationships between the catalyst’s properties and 1.5-PeD yields were established. Moreover, Co introduction altered the catalyst surface’s Brønsted and Lewis acids content. Density functional theory (DFT) indicated enhanced H 2 adsorption and dissociation due to electro-transfer between Co and Zn species, with a tilted configuration favoring ring opening. Finally, a possible reaction mechanism was proposed. This work provides valuable insights for preparing ultrathin nanoflake ZnCo-LDH catalysts for biomass-derived furfur compound upgrading.
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MICROCHEMICAL JOURNAL
·
2024
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IF 4.9
Aijuan Xie,Linghui Cao,Tianyu Shen,Yuanxinyi Zhou,Haoye Wang,Shiping Luo
As para -aminophenol (PAP) is toxic to humans, causing skin irritation, eye damage, and central nervous system depression, and it can form as a degradation product of paracetamol (PAT) under certain conditions, the simultaneous determination of PAP and PAT is crucial. This work presents the fabrication of three-dimensional ZnCo 2 O 4 @Fe 3 O 4 /MWCNTs hybrid for the simultaneous determination of PAP and PAT using ZIF-8/67@Fe 3 O 4 as precursor and MWCNTs as conductive substrate. The ZnCo 2 O 4 @Fe 3 O 4 /MWCNTs/GCE sensor exhibits linear ranges 1.0–150.0 μM with detection limits of 0.033 μM and 0.018 μM for PAP and PAT, respectively. The developed sensor was successfully used for the determination of PAP and PAT in acetaminophen tablets and lake water with satisfactory results.
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Materials Today Chemistry
·
2024
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IF 6.7
Shihong Lin,Bingyan Chen,Ying Xu,Zhiyu Li,Yuanrong Liao,Jun Wang,Peiyan Yu,Yang Zhang
Synergistic surface-enhanced Raman spectroscopy (SERS) substrates, leveraging the combined strengths of electromagnetic enhancement (EM) and chemical enhancement (CM), have been extensively explored in the literature. In this study, we introduce a distinctive approach to fabricating core@shell structures, specifically employing silver nanowire @ zeolite imidazole framework-8 (AgNW@ZIF-8) as synergistic SERS substrates. Notably, these substrates offer meticulous control over shell thickness through a straightforward post-synthesis procedure. Utilizing Ag nanowires as the plasmonic core, selected for their broader localized surface plasmon resonance (LSPR) absorption range compared to nanoparticles , we encapsulate them within ZIF-8, a metal-organic framework (MOF) recognized for its proficient charge transfer (CT) properties. Our investigation encompasses the SERS performance across various Raman-active molecules, considering their diverse sizes and distinct frontier molecular orbitals (FMO) energy levels. Additionally, we systematically explore the influence of alterations in shell thickness on SERS outcomes and scrutinize the impact of probe orientation. This comprehensive study not only advances the understanding of synergistic effects intrinsic to MOFs-metal SERS substrates but also provides valuable insights for the rational design of highly sensitive substrates tailored for practical applications.
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CONSTRUCTION AND BUILDING MATERIALS
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2025
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IF 8
Dandan Yan,Min Li,Chunxiang Qian
Phase change materials are used in cementitious materials to reduce the hydration temperature rise and thus inhibit the temperature cracks generation. However, the influence mechanism of phase change materials on the hydration properties of cementitious materials is still unclear. In this study, ZIF-8-based composite phase change materials (CPCM) were added to the Portland cement (PC) clinker-anhydrite (C$)-calcium sulfoaluminate (CSA) cement ternary system (PCCSA) in the form of admixtures. The effects of controlling the phase change temperatures, dosages of CPCM and hydration temperatures on the hydration exothermic characteristics, hydration products and the compressive strength development in the PCCSA composite system were investigated. CPCM addition reduced the hydration exothermic rate and cumulative heat release of the ternary system, especially when the phase change temperature of CPCM was 25.8 ℃, and the larger the dosage, the more obvious the reduction effect. In addition, CPCM did not participate in the hydration reaction of the system, but promoted the formation of CH and AFm. Simultaneously, the compressive strength of the PCCSA system paste containing CPCM decreased due to increased porosity in the paste. Furthermore, elevated hydration temperature significantly improved the hydration rate of the system, while reduced the hydration degree, and the hydration products types of the system were not affected by the hydration temperatures. This study results are fundamental for predicting the hydration behavior of cement systems containing CPCM and promoting the application of composite phase change materials in cementitious materials.
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CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Xiaoqian Meng,Rui Gao,Ming Zheng,Xin Zhou,Xianfa Zhang,Xiaoli Cheng,Yingming Xu,Shan Gao,Lihua Huo
Real-time monitoring of chlorine gas (Cl 2 ) with a strong irritating odor is an indispensable means of avoiding its contamination of the air and harm to the body. To achieve this purpose, a novel gas-sensitive material capable of detecting low concentrations of Cl 2 at near room temperature is developed in this paper. ZIF-8 with a kinetic diameter of 3.4 Å in the designed ZnO@ZIF-8 composites is able to sieve gas molecules with different kinetic diameters, enabling effective improvement of the selectivity of the gas-sensitive materials. In addition, the porous structure of ZIF-8 can provide more reactive sites, which is conducive to improving gas adsorption capacity and providing of channels for gas diffusion. In this study, ZnO@ZIF-8 heterojunction composites are prepared by combining the advantages of ZnO and ZIF-8, which provides a new method for real-time monitoring of low concentrations of Cl 2 , and also has potential practical applications in fields such as environmental monitoring and industrial safety.
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