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ZIF-67
Journal of Environmental Sciences · 2022 · IF 6.796

Highly efficient Hg2+ removal via a competitive strategy using a Co-based metal organic framework ZIF-67

Jiacheng Zhou,Hao Zhang,Tianying Xie,Ye Liu,Qicheng Shen,Jie Yang,Limei Cao,Ji Yang

The stronger coordination ability of mercury ions with organic ligands than the metal ions in metal organic framework (MOFs) provides an accessible way to separate mercury ions from solution using specific MOFs. In this study, a Co-based MOF (ZIF-67, Co(mIM) 2 ) was synthesized. It did not introduce specific functional groups, such as -SH and -NH 2 , into its structure through complicated steps. It separate Hg 2+ from wastewater with a new strategy, which utilized the stronger coordination ability of Hg 2+ with the nitrogen atom on the imidazole ring of the organic ligand than the Co 2+ ions. Hg 2+ replaced Co 2+ nodes from ZIF-67 and formed a more stable precipitate with mIM. The experimental results showed that this new strategy was efficient. ZIF-67 exhibited Hg 2+ adsorption capacity of 1740 mg/g, much higher than the known MOFs sorbents . mIMs is the reaction center and ZIF-67 can improve its utilization. The sample color faded from purple to white due to the loss of cobalt ion. It is a great feature of ZIF-67 that allows users to judge whether the sorbent is deactivated intuitively. ZIF-67 can be sustainable recycled by adding organic ligands to the solution after treatment due to its simple synthesis method at room temperature. It's a high-efficient and sustainable sorbent for Hg 2+ separation from wastewater.

CAS / MDL: 10026-22-9 67-56-1
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2022 · IF 4.598

A novel electrochemiluminescent immunosensor for the detection of NT-proBNP based on a Au/ZIF-67 nanocomposite

Qian Luo,Xiaomin Qian,Xiaona Mi,Yifeng Tu

A new type of immunosensor was prepared by using a gold nanoparticles/aminozeolitic imidazolate framework-67 nanocomposite (AuNPs/ZIF-67) as the sensing matrix and luminol as the signaling probe to detect the heart failure biomarker N -terminal probrain natriuretic peptide (NT-proBNP). The hybrid nanocomposite was deposited on the surface of indium tin oxide (ITO)-coated glass via the linkage of 3-aminopropyltrimethoxysilane (APTMS); thereafter, the NT-proBNP antibody was immobilized to endow biological specificity, and bovine serum albumin was used to block residual active sites. The resultant sensor has an excellent response when NT-proBNP was attached to the antibody via immunoreaction; here, the output signal was reduced because of the depressed mass transportation of the electrochemiluminescence (ECL) probe and electron transference. The resultant ECL immunosensor displayed a broad linear range from 10 pg/mL to 50 ng/mL, and the low detection limit was 0.74 pg/mL. The ECL immunosensor also has good specificity, stability and reproducibility and can be used to detect NT-proBNP in real blood samples.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Electrocatalytic hydrogenation of nitrogenous heterocyclics using Co-based nanoparticles-embedded N-doped carbon derived from ZIF-67

Yu Liu,Shuai Yang,Xinyu You,Linlin Qin,Yiming Qin,Wenwen Zhang,Wenyan Liang

Electrocatalytic hydrogenation (ECH) has been used as a novel approach for the synthesis of organic compounds. Hence, ZIF-67 was selected as a precursor in this study to synthesize a series of electrodes. The ECH effects were assessed on pyridine and diazines. The results showed a significant influence of carbonization temperature and time on the electrocatalyst activity. A temperature of 400 °C was found not high enough for the synthesis of the electrocatalysts, and a long time of 4 h at 800 °C resulted in damage to the spatial structure of the electrocatalyst. The optimal electrocatalyst was obtained under 800 °C and 2 h (Co/NC-800–2). The polyhedral Co/NC-800–2 (20–200 nm) had the N-doped graphitic-carbon shell with embedded Co/CoN/Co 3 O 4 nanoparticles . The onset potential and overpotential (at 10 mA cm −2 ) were estimated to respectively 64 and 155 mV versus hydrogen evolution reaction (HER), with a Tafel value of 62 mV dec −1 . The ECH on pyridine and diazines revealed a positive correlation between ECH effect and HER activity. Co/NC-800–2 possessed excellent ECH activity toward pyridine and pyrazine at − 0.3 V (vs. RHE). N–Co, pyridinic-N, and graphitic-N acted as active sites during electrocatalysis . The N-doped graphitic-carbon promoted the charge transfer during ECH processes.

CAS / MDL: 110-86-1
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2022 · IF 7.139

Ni@NC@NiCo-LDH nanocomposites from a sacrificed template Ni@NC@ZIF-67 for high performance supercapacitor

Yuan Chen,Hao Guo,Fan Yang,Ning Wu,Junye Zhang,Liping Peng,Bingqing Liu,Zhilan Pan,Wu Yang

A metal porous carbon (Ni@NC) supported nickel/cobalt layered double hydroxide (NiCo-LDH) (Ni@NC@NiCo-LDH) with a cauliflower morphology was synthesized by a successive double template method . At first a nickel metal-organic framework (Ni-MOF) was prepared and used as a sacrifice template to produce metal porous carbon (Ni@NC). Then the prepared conductive porous carbon material was exploited as a substrate for in-situ growing of ZIF-67 on its surface. Lastly the obtained Ni@NC@ZIF-67 was further used as a sacrifice template to prepare the final electrode material Ni@NC@NiCo-LDH by Ni 2+ etching and co-precipitation. The cooperation of Ni@NC with excellent conductivity and NiCo-LDH with superior pseudocapacitive property yielded a synergistic effect , which effectively improved the electrochemical performance of the resulted electrode material. And the special flower morphology exposed more redox active sites and provided proper charge transport path for enhanced electrochemical performance. The prepared Ni@NC@NiCo-LDH exhibited a high specific capacitance of 1761.8 F·g −1 at the current density of 1 A·g −1 . The assembled Ni@NC@NiCo-LDH//AC asymmetric supercapacitor also displayed an acceptable energy density (39.27 Wh·kg −1 at the power density of 757.21 W·kg −1 ) and ultrahigh cycling stability (94.74% capacitance retention after 25000 cycles at 10 A g −1 ).

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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2021 · IF 4.539

Efficient removal of crystal violet by polyacrylic acid functionalized ZIF-67 composite prepared by one-pot synthesis

Xiaoxun Liu,Jilin Zhang,Yi Cheng,Xiaoya Zhao,Zi Dai,Guixia Liu

The adsorption of organic dyes by sorbents is one of the effective ways to resolve the problem of dye wastewater treatment . However, the limited adsorption capacity of adsorbents has always been a crucial factor that plagues the development and utilization of adsorbents. Herein, aiming at efficient adsorption for crystal violet (CV), polyacrylic acid (PAA) was incorporated into zeolitic imidazoline frameworks (ZIF-67) through an easy and environmentally friendly aqueous phase synthesis process at room temperature to synthesize adsorbent ZIF-67-PAA. Compared to pure ZIF-67, the obtained adsorbent ZIF-67-PAA showed excellent adsorption performance and the maximum adsorption capacity of CV can reach 1606 mg g −1 . The adsorption process is spontaneous and conformed to the Langmuir isotherm model and the pseudo-second-order kinetic model . The results show that the prepared ZIF-67-PAA is a potential and efficient adsorbent for CV removal.

CAS / MDL: 10026-22-9 693-98-1
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CELLULOSE · 2021 ·Vol. 28 ·期 6 ·3585-3598 · IF 5.044

Facile in situ synthesis of ZIF-67/cellulose hybrid membrane for activating peroxymonosulfate to degrade organic contaminants

Zhang Sufeng,Zhao Mengke,Li Hao,Hou Chen,Du Min

In recent years, cobalt-based metal–organic frameworks (MOFs) have been used as catalytic materials to degrade organic contaminants in sulfate radical-based advanced oxidation processes (SR-AOPs). However, separating and recovering granular MOFs from the reaction system is difficult. Loading MOFs on the host material is currently the most effective way to promote their recyclability. Most reported aerogel materials are characterized by excessively long preparation and drying cycles. Considering this, herein, we report an in situ grown method to fabricate a ZIF-67/cellulose hybrid membrane, which was used as a catalyst for activating peroxymonosulfate to generate \({\text{SO}}_{4}^{ - }\cdot\) and · OH, resulting in the contaminants degradation. The catalytic results showed that the hybrid membrane/PMS system could degrade the methylene blue and rhodamine B within 1 min. In addition, the separation and recovery problems were solved. The ZIF-67/cellulose hybrid membrane with outstanding degradation of contaminants expands the application of MOFs/cellulose hybrid materials for wastewater purification via SR-AOPs. Graphic abstract

CAS / MDL: 693-98-1
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JOURNAL OF MOLECULAR LIQUIDS · 2021 · IF 6.165

Synthesis of novel Ag@ZIF-67 rhombic dodecahedron for enhanced adsorptive removal of antibiotic and organic dye

Summaira Saghir,Zhenggang Xiao

Ag@ZIF-67 was successfully prepared by using a facile and fast method at room temperature and characterized by a variety of techniques. Results indicate that prepared Ag@ZIF-67 contains a very beautiful morphology with a great active specific surface area than solo ZIF-67. The prepared Ag@ZIF-67 contains a greater pore size, which is 1.564 nm with increased functional sites. The adsorption performance of Ag@ZIF-67 was further studied with the removal of Minocycline (MC) and methyl orange (MO) from polluted water. Various adsorption parameters, such as contact time, adsorbent dosage, pH, and initial concentrations of MC and MO, were optimized. The kinetics parameters of the adsorption process were determined by applying the pseudo first-order kinetic model (PFO) and pseudo second-order (PSO) kinetic model. In the case of MC, adsorption isotherm data matched well with Freundlich as compared to Langmuir and Temkin model. While in the case of MO, adsorption isotherm data followed the Langmuir model as compared to the Freundlich and Temkin model. Ag@ZIF-67 was found to be an efficient adsorbent for the adsorption of MC and MO, having 938.4 mg/g and 994.6 mg/g adsorption capacity, which is higher than reported adsorbents.

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Journal of Environmental Chemical Engineering · 2020 · IF 4.3

Influence of Ca2+ on phosphate removal from water using a non-core-shell Fe3O4@ZIF-67 composites

Yinghao Xue,Ping Xiang,Yuzhu Jiang,Huilan Lian,Jingyu Mo,Mengying Li

Excessive phosphate in surface water can spur the growth of organism, which put a threat on the bio-safety of drinking water. Different from previous study, sodium acetate (NaAc) was used as modification agent of Fe 3 O 4 , then the magnetic Fe 3 O 4 @ZIF-67 composites with a non-core-shell sturture were synthesized. According to ZIF-67 loading and phosphate adsorption of synthesized Fe 3 O 4 @ZIF-67, the Fe 3 O 4 @ZIF-67 composites with a Co 2+ /Fe 3 O 4 molar ratio of 1:2 was taken into further evaluation. Fe 3 O 4 @ZIF-67 composites exhibited satisfactory adsorption performance and easy magnetic recovery, and the sorption capacity reached 116.59 mg P/g within 180 min (C 0 = 20 mg P/L, 298 K). The maximum adsorption capacity of phosphate was obtained at the neutral pH, and not significantly interfered with ions of K + , Mg 2+ , NO 3 − and SO 4 2- . Remarkably, Fe 3 O 4 @ZIF-67 described enhanced phosphate adsorption ability in the presence of Ca 2+ . To investigate the role of Ca 2+ , two modes (preloading and addition) of Ca 2+ dosing were examined and the improved adsorptive performance could be owing to the synergistic eff ;ect of adsorption and Ca-P micro-precipitation on the surface of Fe 3 O 4 @ZIF-67. During the regeneration process, the performance of desorbent was evaluated by phosphate releasing and secondary adsorption, and the absence or presence of Ca 2+ would have a significant impact on the selection of desorption solution.

CAS / MDL: 693-98-1 7778-77-0
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CHINESE CHEMICAL LETTERS · 2020 · IF 4.632

ZIF-67 derived hollow Ni-Co-Se nano-polyhedrons for flexible hybrid supercapacitors with remarkable electrochemical performances

Guangmeng Qu,Xixi Zhang,Guotao Xiang,Yunrui Wei,Jiangmei Yin,Zonghua Wang,Xiaoli Zhang,Xijin Xu

Nano-polyhedral NiSe 2 /CoSe 2 (Ni-Co-Se) with hollow architectures are synthesized by selenizing the precursors of Ni-Co bimetallic hydroxides that are directly derived from ZIF-67. The as-fabricated Ni-Co-Se electrodes exhibit high specific capacitance of 1668 F/g at 1 A/g accompanying with outstanding rate capability (about 82.8% retention of the initial capacity at 20 A/g). The corresponding Ni-Co-Se//AC all-solid-state hybrid supercapacitors are assembled by directly using the Ni-Co-Se on carbon fabric as the positive electrode, which deliver high energy density and power density (38.5 Wh/kg at 802.1 W/kg, 32.0 Wh/kg at 8008.8 W/kg), excellent cyclic stability (82.3% retention after 5000 cycle) and robust mechanical flexibility (no obvious attenuation at bending to different angles). This work will provide a new and smart route for constructing transition metal selenides for supercapacitor devices.

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CERAMICS INTERNATIONAL · 2023 · IF 5.2

ZIF-67 derived Co@carbon nanotubes anchored on carbon fiber for efficient microwave absorption and mechanical enhancement

Chengjuan Wang,Haotian Jiang,Bowen Cui,Xiaodan Xu,Yanxiang Wang,Chengguo Wang

Rational design of multifunctional and high-performance electromagnetic wave (EMW) absorbers is highly desirable but still remains a challenge. Herein, the 3D heterostructural Co@carbon nanotubes/carbon fiber (Co@CNTs/CF) hybrids derived from ZIF-67/CF were successfully fabricated via the in-situ synthesis of ZIF-67 on CF and subsequent catalytic chemical vapour deposition. Intriguingly, the as-obtained composites acquire adjustable EMW absorption and favorable mechanical properties simultaneously. Specifically, taking advantage of adequate conductive paths, plentiful heterogeneous interfaces, suitable defect vacancies, appropriate magnetic loss, as well as optimized impedance matching, Co@CNTs/CF delivers a brilliant EMW absorption intensity of −45.11 dB at only 1.15 mm together with a broad effective absorption bandwidth (EAB) of 4.0 GHz (1.23 mm), and an unexpected minimal reflection loss up to −65.63 dB (3.84 GHz) coupled with an EAB of 3.6 GHz at merely 1.09 mm, respectively. In addition, the tunable EAB can be achieved in 2.6–18 GHz, covering 96 % of the test frequency by changing the absorber thickness from 0.93 to 5.0 mm (29 wt%). Moreover, the maximum radar cross section reduction can reach 48.8 dBm 2 . The uniform layer of CNTs with moderate crystallinity also enables Co@CNTs/CF to improve the tensile strength and Weibull modulus compared to unsized CF. This study paves a novel avenue for developing multifunctional materials based on CF through an efficient, controllable and low-cost approach.

CAS / MDL: 10026-22-9 693-98-1
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JOURNAL OF THE AMERICAN CERAMIC SOCIETY · 2023 ·Vol. 107 ·期 2 ·719-735 · IF 3.9

Black TiO2-g-C3N4 heterojunction coupled with MOF (ZIF-67)-derived Co3S4/ nitrogen-doped carbon hollow nanobox

Mojtaba Rostami,Milad Jourshabani,Fatemeh Davar,Ghodsi Mohammadi Ziarani,Alireza Badiei

In this research, the ultrasound (US) technique was applied as a facile synthesis method for preparing the black TiO 2 -g-C 3 N 4 type II heterojunction, coupled with a Schottky junction MOF (ZIF-67)-derived x wt% Co 3 S 4 /nitrogen-doped carbon (NC) ( x = 3, 10, and 15) with hollow nanobox (HNB) morphology, as a smart nanoheteroarchitecture (NHA) photocatalyst to enhance visible-light photocatalytic activity. Additionally, the solvothermal synthesis route was employed to fabricate the MOF (ZIF-67)-derived Co 3 S 4 /NC cubic hollow nanoboxes (CHNBs) before the pyrolysis process. The black TiO 2 -g-C 3 N 4 wt% Co 3 S 4 /NC (TiCN-15% CoS/NC) NHAs exhibited high photocatalytic activity in degrading methylene blue. The synergetic effect of all components in black TiCN- x wt% CoS/NC NHAs resulted in efficient electron-hole pair separation and charge mobility on Co 3 S 4 /NC HNB and g-C 3 N 4 surfaces, which led to a highly effective recombination rate of charge carriers and an excellent improvement in photocatalytic performance.

CAS / MDL: 16940-66-2
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ACS Omega · 2023 · IF 4.1

Synthesis of Metal–Organic Framework-Based ZIF-8@ZIF-67 Nanocomposites for Antibiotic Decomposition and Antibacterial Activities

Samreen Sadiq,Iltaf Khan,Muhammad Humayun,Ping Wu,Abbas Khan,Sohail Khan,Aftab Khan,Shoaib Khan,Amal Faleh Alanazi,Mohamed Bououdina

Toxic antibiotic effluents and antibiotic-resistant bacteria constitute a threat to global health. So, scientists are investigating high-performance materials for antibiotic decomposition and antibacterial activities. In this novel research work, we have successfully designed ZIF-8@ZIF-67 nanocomposites via sol–gel and solvothermal approaches. The ZIF-8@ZIF-67 nanocomposite is characterized by various techniques that exhibit superior surface area enhancement, charge separation, and high light absorption performance. Yet, ZIF-8 has high adsorption rates and active sites, while ZIF-67 has larger pore volume and efficient adsorption and reaction capabilities, demonstrating that the ZIF-8@ZIF-67 nanocomposite outperforms pristine ZIF-8 and ZIF-67. Compared with pristine ZIF-8 and ZIF-67, the most active 6ZIF-67@ZIF-8 nanocomposite showed higher decomposition efficacy for ciprofloxacin (65%), levofloxacin (54%), and ofloxacin (48%). Scavenger experiments confirmed that •OH, •O2–, and h+ are the most active species for the decomposition of ciprofloxacin (CIP), levofloxacin (LF), and ofloxacin (OFX), respectively. In addition, the 6ZIF-67/ZIF-8 nanocomposite suggested its potential applications in Escherichia coli for growth inhibition zone, antibacterial activity, and decreased viability. Moreover, the stability test and decomposition pathway of CIP, LF, and OFX were also proposed. Finally, our study aims to enhance the efficiency and stability of ZIF-8@ZIF-67 nanocomposite and potentially enable its applications in antibiotic decomposition, antibacterial activities, and environmental remediation.

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