CORROSION SCIENCE
·
2018
·
IF 4.862
Liangliang Xiong,Jianhua Liu,Mei Yu,Songmei Li
A two-dimensional nanocomposite, salicylaldehyde@ZIF-8/GO (SZG), was synthesized by anchoring the ZIF-8 nanoparticles containing the inhibitor salicylaldehyde (SA) on GO nanosheets for corrosion protection of AA2024 aluminum alloy. Its stimuli-responsive release of SA under acid and Al 3+ cations conditions was proved by UV–vis. Electrochemical impedance spectroscopy demonstrated that SZG nanocomposites prominently improved the protection properties of PVB coating by enhanced passive and active protection compared with the controlled samples. The enhanced passive protection derived from the two-dimensional structure of SZG, while inhibitor SA acted the active protection. Quantum chemical calculation clearly clarified the release and inhibition mechanisms of SA.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2019
·
IF 5.107
Tie Gao,Zhenzhen Liu,Haibo Li
Heteroatom doped carbonaceous material has attracted enormous attentions in electrochemical research community due to the replacement of some carbon atoms in the carbon skeleton result in charge redistribution and thus the modification of physiochemical properties. In this work, we proposed a facial approach to synthesize nitrogen and titanium co-doped hierarchical mesoporous carbon ((N, Ti)-HMCs) by employing ZIF-8 as procures for capacitive deionization (CDI) with enhanced performance. The as-prepared (N, Ti)-HMCs exhibits novel cubic structure, high doping content and high specific surface area of 1025.93 m 2 /g. The Raman spectra revealed the presence of abundant structural defects in (N, Ti)-HMCs rather than HMCs which is beneficial to promote the electrosorption. Besides, the electrochemical analysis demonstrated that (N, Ti)-HMCs owns improved specific capacitance and lower resistivity as compared to that of HMCs. Moreover, by examining the CDI performance of (N, Ti)-HMCs in a batch mode experiment, it illustrated high salt removal capacity of 13.89 mg/g at 1.2 V in a 500 mg/L NaCl solutions and outstanding adsorption rate of 3.53 mg/(g·min). Thus, (N, Ti)-HMCs should be proposed as superior electrode materials for enhanced CDI. Our work also strengthens the emphasis on heteroatom doped carbonaceous materials in CDI.
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ANALYST
·
2018
·Vol. 143
·期 12
·2837-2843
·
IF 3.864
Xueping Zhang,Qingqing Wang,Jing Li,Liang Huang,Dengbin Yu,Shaojun Dong
In this work, a novel electrochemical sensor for Cd(II) detection with differential pulse anodic stripping voltammetry (DPASV) is fabricated based on hollow ZnO@nitrogen-doped carbon (H-ZnO@NC) polyhedra, which are prepared from ZIF-8 via in situ tannic acid etching and a subsequent calcination process. The as-obtained H-ZnO@NC exhibits a polyhedral morphology with a well-defined hollow structure and a uniform distribution of elements C, N, O, and Zn in the shell. The unique structure of H-ZnO@NC can provide an enlarged surface area and abundant active sites. Moreover, ZnO has a strong affinity for heavy metals, which can enhance the adsorption capacity of H-ZnO@NC for Cd(II) in the accumulation step of stripping voltammetry, and thus improve the electrochemical sensing performances. As expected, the H-ZnO@NC-based sensor achieves a wide linear range of 0.3–300 μg L−1, a low detection limit of 0.1 μg L−1 (S/N = 3), and exhibits good selectivity as well as high stability and reproducibility. Moreover, the proposed electrochemical sensor can be applied for the determination of Cd(II) in real water samples, obtaining satisfactory results.
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ACS Applied Materials & Interfaces
·
2019
·
IF 8.456
Jialin Shi,Lina Zhang,Nannan Sun,Deng Hu,Qun Shen,Fang Mao,Qiang Gao,Wei Wei
Metal–organic frameworks (MOFs) are promising hosts for catalytic active sites due to their adjustable porosity and framework chemistry. Strategies to improve synergistic effects between the installed sites and the parent MOF are highly desired. Herein, a facile and rapid method for the preparation of xAg@ZIF-8 materials was reported. The materials were systematically characterized and used as catalysts for carboxylation of terminal alkynes via direct insertion of CO2 to the C(sp)–H bond (CTACO2). It was found that the integrity of the ZIF-8 structure could be retained upon Ag loading, but short-range crystalline ordering was modified. Two types Ag species could be installed, namely, highly dispersed Ag(I) in the backbone (AgHD) and aggregated Ag(0) nanoparticles on the outer surface (AgNP). The AgNP sites are highly effective for the activation of terminal alkynes due to its high accessibility, while the AgHD-modified ZIF-8 framework worked as a CO2 reservoir with enhanced affinity. Combination of these factors translated to high activity in the CTACO2 process, the measured turnover frequency and time yield are among the highest among most heterogeneous catalysts.
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ACS Applied Materials & Interfaces
·
2025
·
IF 8.2
Meixuan Li,Fengzhen Yang,Kaiyuan Jia,Qiang Zhang,Weichao Zheng,Hui Chen,Ming Liao,Jianhan Lin,Lei Wang
Bioaerosol infections containing pathogenic viruses and bacteria have resulted in significant economic losses and posed a serious threat to public health, as evidenced by outbreaks of coronavirus disease and avian influenza. Consequently, the sampling and screening of bioaerosols are crucial for the prevention of bioaerosol-borne diseases. In this study, an ultrasensitive biosensor based on zeolitic imidazolate framework-8-melamine foam (ZIF-8-MF) was innovatively developed for the specific capture and in situ detection of bioaerosols. The bacterial bioaerosols were collected by a wet cyclone into phosphate-buffered saline (PBS) buffer at a high collection rate, achieving a satisfactory collection efficiency of ∼80% within 10 min. The target bacteria collected in the PBS buffer were specifically captured and effectively concentrated using immune ZIF-8-MF. The gold@platinum nanozymes (GPNs) were employed to specifically label the captured target bacteria and efficiently amplify the biological signal. And the resulting colorimetric signal was analyzed via a self-developed smartphone application (App). This biosensor demonstrated the capability to detect bioaerosols containing Salmonella typhimurium in the range of 1.6 × 102–1.6 × 105 CFU/m3 within 1.5 h, with a detection limit as low as 100 CFU/m3. Compared with other bioaerosol detection methods, the biosensor offered advantages such as high collection rate, specific capture, efficient concentration, and in situ detection, positioning it as a highly promising and practical tool for the monitoring of bioaerosols containing diverse pathogenic bacteria.
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MOLECULES
·
2024
·Vol. 29
·期 2
·307
·
IF 4.2
Zixuan Li,Qinghong Shi,Xiaoyan Dong,Yan Sun
Co-immobilization of laccase and mediator 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) for wastewater treatment could simultaneously achieve the reusability of laccase and avoid secondary pollution caused by the toxic ABTS. Herein, Fe-induced mineralization was proposed to co-immobilize laccase and ABTS into a metal–organic framework (ZIF-8) within 30 min. Immobilized laccase (Lac@ZIF-8-Fe) prepared at a 1:1 mass ratio of Fe2+to Zn2+exhibited enhanced catalytic efficiency (2.6 times), thermal stability, acid tolerance, and reusability compared to free laccase. ABTS was then co-immobilized to form Lac+ABTS@ZIF-8-Fe (ABTS = 261.7 mg/g). Lac@ZIF-8-Fe exhibited significantly enhanced bisphenol A (BPA) removal performance over free laccase due to the local substrate enrichment effect and improved enzyme stability. Moreover, the Lac+ABTS@ZIF-8-Fe exhibited higher BPA removal efficiency than the free laccase+ABTS system, implying the presence of a proximity effect in Lac+ABTS@ZIF-8-Fe. In the successive malachite green (MG) removal, the MG degradation efficiency by Lac@ZIF-8-Fe was maintained at 96.6% at the fifth reuse with only an extra addition of 0.09 mM ABTS in each cycle. As for Lac+ABTS@ZIF-8-Fe, 58.5% of MG was degraded at the fifth cycle without an extra addition of ABTS. Taken together, this research has provided a novel strategy for the design of a co-immobilized laccase and ABTS system for the degradation of organic pollutants.Keywords:laccase;mediator;co-immobilization;MOFs;organic pollutants;biodegradation
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MICROCHEMICAL JOURNAL
·
2015
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IF 2.746
Zhirong Zou,Shanling Wang,Jia Jia,Fujian Xu,Zhou Long,Xiandeng Hou
In this work, magnetic Fe 3 O 4 @ZIF-8 core-shell nanoparticles (MNPs) were employed for effective adsorption of inorganic arsenic for preconcentration , with adsorption mechanism thoroughly discussed. The adsorbed inorganic arsenic was easily separated by a magnet along with the MNPs from the sample matrix, with possible matrix interference eliminated. The MNPs were then completely dissolved in hydrochloric acid prior to the determination of inorganic arsenic by hydride generation-atomic fluorescence spectrometry. The Fe 3 O 4 @ZIF-8 MNPs were prepared with a facile step-by-step assembly method in aqueous solution at room temperature . Under the optimized conditions, the sensitivity for inorganic arsenic determination was significantly increased through preconcentration, with satisfactory analytical merits obtained.
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2016
·Vol. 163
·期 6
·H459
·
IF 3.014
Min Jiang,Xueping Cao,Ping Liu,Tongping Zhang,Jianming Zhang
As novel N-doped carbon precursors, zeolitic imidazolate framework-8@polyvinyl pyrrolidone (ZIF-8@PVP) composites were designed and synthesized. Direct carbonization of ZIF-8@PVP composites at a high temperature produced the nitrogen-doped porous carbon materials (named as CP1000). And the electrocatalytic abilities of the corresponding carbonized products toward oxygen reduction reaction in alkaline solution were investigated. In comparison with the carbonized product of pure ZIF-8 (named as C1000), CP1000 possesses the higher specific surface area and total pore volume. By adjusting the initial dosage of PVP, three kinds of CP1000 with different size and N content were prepared. It was found that the high specific surface area and favorable quaternary-N species in CP1000 sample played an active role in catalyzing oxygen reduction reaction (ORR).
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JOURNAL OF NANOPARTICLE RESEARCH
·
2017
·Vol. 19
·期 8
·1-11
·
IF 2.02
Cheong Ling-Zhi,Wei Yayu,Wang Hongbin,Wang Zhiying,Su Xiurong,Shen Cai
Zeolitic imidazolate frameworks (ZIF) represent one of the metal organic frameworks (MOF) with high potential for enzyme immobilization due to their exceptional chemical and thermal stability, negligible cytotoxicity, and easy synthesis under mild biocompatible conditions. Amine-functionalized ZIF-8 (An-ZIF-8) are capable of forming multipoint attachment via hydrogen bonding with lipase which will immobilize and further enhance stabilization of lipase. In addition, increased hydrophilicity of An-ZIF-8 will increase partitioning of An-ZIF-8 immobilized lipase at the aqueous/organic interface which enable lipase to expose its active site and retain its catalytic activity at its highest. Present study reports the use of ZIF-8 and An-ZIF-8 nanoparticles as carrier for Burkholderia cepacia lipase (BCL), compares the ester hydrolysis and transesterification activities of immobilized lipase with those of free lipase, and evaluates the reusability and recovery rate of the immobilized lipase. An-ZIF-8 nanoparticles (average 130.42 ± 0.55 nm) were facilely synthesized via mixing ZIF-8 nanoparticles with ammonia hydroxide solution. Despite having similar characteristics of high crystallinity and forming cuboid-like particles, An-ZIF-8 demonstrated significantly ( P < 0.05) lower Brunauer-Emmett-Teller (BET) surface area and higher thermal stability than ZIF-8. BCL were successfully immobilized on ZIF-8 (BCL@ZIF-8) and An-ZIF-8 (BCL@An-ZIF-8) nanoparticles with an average lipase loading rate of ~ 8 mg/g MOF. The immobilized BCL demonstrated no significant differences in terms of esters hydrolysis and transesterification activities with those of free BCL. BCL@An-ZIF-8 demonstrated superior catalytic stability in comparison to BCL@ZIF-8 with retainment of more than 80% of its initial hydrolysis and transesterification activity for at least 10 repeated runs. In addition, more than 80% of the BCL@An-ZIF-8 can be easily recovered during each cycle of the reusability test through simple centrifugation.
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JOURNAL OF MEMBRANE SCIENCE
·
2017
·
IF 6.035
Xuehua Ruan,Xinfang Zhang,Xuhang Liao,Xiaobin Jiang,Yan Dai,Xiaoming Yan,Gaohong He
Zeolitic imidazolate framework-8 (ZIF-8) with regular pore size (~ 0.34 nm) is widely attempted for gas separation membranes based on size sieving. However, the prospect is subjected to fabricating the continuous ZIF-8 membranes with high mechanical stability and uniformity. In response, an adhesive layer of Zn(II)-doped polydopamine (Zn-PDA) is pre-coated on the stainless steel nets in this work to improve ZIF-8 nucleation and growth. Zn-PDA layer shows high tolerance to ultrasonic agitation and heated methanol (system for ZIF-8 synthesis), little dissolution within 24 h, which supplies a high stable surface for ZIF-8 growth. Furthermore, the Zn(II) doped in PDA layer is opportunely serving as the even-distributed ZIF-8 nucleation starting sites, verified with the EDX and FE-SEM images for the aggregated Zn(II) clusters and the nascent ZIF-8 crystals. Therefore, an indented and hinged boundary is constructed between ZIF-8 and substrate to enhance the mechanical stability. The FE-SEM images after ultrasonic agitation show that the continuous ZIF-8 membranes prepared on Zn-PDA layers can tolerate the deformation to a certain extent. Finally, the prepared ZIF-8 membranes behave excellently with α H2/CO2 = 9.9, α H2/CO = 17.2, α H2/CH4 = 26.0, and permeation rate J H2 = 3980 GPU. This work supplied a useful approach to enhance mechanical stability and uniformity of defect-free ZIF-8 membranes.
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Advanced Healthcare Materials
·
2024
·
IF 10
Jie Tang,Yu Li,Xuefeng Hu,Wei Hua,Haoning Xu,Li Li,Fujian Xu
The systemic use of tranexamic acid (TA) as an oral drug could bring adverse reactions, while intradermal injection leads to pain and a risk of infection. Moreover, it is difficult for highly hydrophilic TA to penetrate the skin barrier that contains lots of hydrophobic lipid compounds, which poses enormous restrictions on its topical application. Current transdermal TA delivery strategies, are suffering from low drug load rates, plus its synthesis complexity, time-consumption etc., adding to the difficulty of TA topical application in clinical therapeutics. To increase the penetration of TA, a novel approach using TA-loaded ZIF-8 (TA@ZIF-8) was developed. The encapsulation efficiency of TA@ZIF-8 reached nearly 25% through physical adsorption and chemical bonding of TA indicated by theoretical simulation and the improved TA penetration was elevated through activating the aquaporin-3 (AQP-3) protein. Additionally, in vivo and in vitro experiments have demonstrated the preponderance of TA@ZIF-8 for penetration ability and the advantages in intracellular uptake, minor cytotoxicity, and inhibition of melanogenesis and inflammatory factors. Moreover, clinical trials have demonstrated the safety and efficacy of TA@ZIF-8 in the treatment of melasma and rosacea. This work presents a potential topical application of TA, free from the safety concerns associated with systemic drug administration. This article is protected by copyright. All rights reserved
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2024
·
IF 7.7
Jiayu Ouyang,Xuefeng Zhang,Xinmiao Qi,Caichao Wang,Yao Yuan,Xiangjing Xie,Jianzheng Qiao,Xin Guo,Yiqiang Wu
To address the issue of bisphenol A (BPA) contamination in wastewater, a novel hydrogel, sodium alginate/cellulose nanofibrils/ZIF-8 composite hydrogel (SCZC), was synthesized for efficient BPA removal. The SCZC exhibited an exceptional adsorption capacity of 1696 mg/g, aligning well with both Langmuir and pseudo-second-order models. Furthermore, it exhibited remarkable regeneration properties, maintaining 89.1 % of its adsorption capacity even after undergoing five adsorption-desorption cycles. The synthesized SCZC also acted as a fluorescent sensor for detecting BPA, employing dynamic quenching and offering linear detection ranges of 10–100 mg/L and 0.2–1.0 μg/L, with a low detection limit of 0.06 μg/L. Analysis of adsorption and detection mechanisms revealed that SCZC's exceptional performance could be attributed to the three-dimensional (3D) porous structure formed by sodium alginate and cellulose nanofibrils. Economic analysis indicated that SCZC, in comparison to commercially activated carbon, was relatively inexpensive. This study introduces a novel approach for designing and preparing a sodium alginate-based hydrogel incorporating metal-organic frameworks, offering simultaneous BPA detection and removal capabilities.
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