Polymers
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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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SEPARATION AND PURIFICATION TECHNOLOGY
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2024
·
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
·
2016
·
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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CHEMISTRY-A EUROPEAN JOURNAL
·
2017
·Vol. 23
·期 40
·9517-9524
·
IF 5.317
Peiyuan Zeng,Jianwen Li,Ming Ye,Kaifeng Zhuo,Zhen Fang
Graphical Better batteries : Co 9 S 8 /N-C hollow spheres were successfully synthesized through synchronous pyrolysis and sulfurization of ZIF-67 (see figure). These structures deliver a distinguished performance when applied as the anode in lithium-ion batteries. Co 9 S 8 is considered a promising candidate as the anode material in lithium-ion batteries (LIBs) because of its remarkable electrical conductivity, high theoretical capacity, and low cost. However, the practical application of Co 9 S 8 is greatly restricted because of its poor cycling stability and rate performance, which result mainly from the large volume expansion and dissolution of the polysulfide intermediates during the charge/discharge process. In this report, Co 9 S 8 embedded in N-rich carbon hollow spheres are successfully designed and synthesized through an in situ pyrolysis and sulfurization process, employing the well-known ZIF-67 as the precursor and ethanethiol as the sulfur source. Co 9 S 8 nanoparticles embedded in the N-rich hollow carbon shell exhibit excellent lithium storage properties at a high charge/discharge rate. A discharge capacity of 784 mAh g −1 is obtained upon battery testing at a current density of 1 C (544 mA g −1 ). Even upon cycling at a current density of 4 C, the as-prepared Co 9 S 8 /N-C can still deliver a discharge capacity of 518 mAh g −1 . The excellent battery performance can be attributed to the hollow structure as well as the N-rich carbon encapsulation. Moreover, this metal–organic framework sulfurization route also shows good generality for the synthesis of other metal sulfide–carbon composites such as ZnS/N-C and Cu 2 S/C.
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APPLIED CATALYSIS B-ENVIRONMENTAL
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2016
·
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
·
2024
·
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
·
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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JOURNAL OF HAZARDOUS MATERIALS
·
2024
·
IF 12.2
Shiyang Li,Chenchen Zheng,Longdou Tu,Dajian Cai,Yangxiang Huang,Congjie Gao,Yeqiang Lu,Lixin Xue
Tight ultra-filtration (TUF) membranes were constructed by in situ growing zinc imidazole frameworks micro-crystalline leaves (ZIF-L) in polyethylene imine (PEI) and polydopamine (PDA) deposit layers on porous polyethylene (PE) substrates. The effects of preparation conditions on the surface physical and chemical structures as well as on the dye/salt separation performance of the formed TUF membranes were systematically investigated. By inserting selective water permeation channels and increasing contacting surface areas, in situ-grown ZIF-L arrays tightly cross-linked in the coating matrix greatly increased water permeation without trading off dye/salt retention selectivity. The morphology of the included ZIF-L particles could be varied by adjusting the ligand/Zn molar ratio (α) in the preparation processes. Optimized PDA-PEI/ZIF-L@PE TUF membranes containing ZIF-L of cross-cross block morphology showed very high pure water permeability of 180 ± 20 L·m −2 ·h −1 ·bar −1 (LMHB) and retention selectivity (S CR/Na2SO4 and S MB/Na2SO4 ) of 267 and 43, respectively, as well as excellent stability and anti-fouling properties.
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Materials Today Chemistry
·
2024
·
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
·
2025
·
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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JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
·
2024
·
IF 5.9
Yi Guo,Jinchao Chen,Chunmei Gao,Shifeng Ji,Yunqing Xing,Wenjing Tan
In this paper, ZIF-L was blended with citric acid (CA) and polyethersulfone (PES) to prepare a casting solution. A novel negatively charged ultrafiltration (UF) membrane (ZIF-L/CA/PES) was obtained using the reverse thermally induced phase separation (RTIPS) method. The hydrophilic carboxyl groups present in CA not only imparted high hydrophilicity and negative charge to the membrane surface, enhancing the membrane’s selectivity and contamination resistance, but also created an acidic environment to attack the Zn atoms in ZIF-L by the ionized H + from CA, resulting in the generation of micro-defective pores and an improvement in permeability. Additionally, the results showed that membranes generated through the RTIPS process exhibit uniform porous surfaces and spongy cross-sections, enhancing membrane performance. The optimized membranes demonstrated the capability to achieve a pure water flux of up to 2267 L/m 2 h with 93.1 % humic acid (HA) retention, and a remarkable membrane flux recovery rate of 75.8 %, suggesting the crucial roles played by CA and ZIF-L in the separation process. In conclusion, hydrophilic anti-fouling UF membranes with a high negative charge and excellent permeation selectivity were fabricated by establishing micro-defective channels through the incorporation of carboxylic acid and ZIF-L, combined with the RTIPS process.
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Advanced Science
·
2024
·
IF 14.3
Yanghai Gui,Jintao Wu,Di Zhao,Kuan Tian,Shuaishuai Zhao,Huishi Guo,Xiaoyun Qin,Xiaomei Qin,Dongjie Guo,Yun Wang
H 2 S gas sensors with facile preparation, low detection limits, and high selectivity are crucial for environmental and human health monitoring. However, it is difficult to maintain a high response of H 2 S gas sensors under high humidity in practical applications. To face this dilemma, a layer-by-layer growth method is applied to in situ prepare a nanostructured Co(CO 3 ) 0.5 (OH)·0.11H 2 O/WO 3 coated by a hydrophobic hierarchical ZIF-67 as the H 2 S sensor. This novel composite exhibits excellent humidity immunity without sacrificing the excellent sensitivity and selectivity of H 2 S. At a low operating temperature of 90 °C, a remarkable response value of 1052.3 to 100 ppm H 2 S has been achieved, which is 779 and 9.36 times higher than that of pure WO 3 and Co(CO 3 ) 0.5 (OH)·0.11H 2 O/WO 3 , respectively. More importantly, an 82.2% relative response value remains at a high humidity of 75%RH. The sensing mechanisms are investigated using gas chromatography-mass spectrometry (GC-MS), which revealed that the reaction products are H 2 O and SO 2 . The high humidity immunity and fast response of the Co(CO 3 ) 0.5 (OH)·0.11H 2 O@ZIF-67/WO 3 demonstrate the layer-by-layer in situ synthesis method holds the potential application for the development of high-performance WO 3 -based H 2 S sensors.
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