NEW JOURNAL OF CHEMISTRY
·
2022
·Vol. 46
·期 6
·2653-2661
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IF 3.925
Long Jin,Feng Liu,Jian-hua Wu,San-Jian Ma,Juan-Hong Li,Yong-Jing Tian,Xin Liu,Zi-Xia Lin
A novel improved Fenton system named MHACF-UiO-66(Zr) was constructed under normal temperature and pressure based on the reduction of FeIII accelerated by hydrogen. The regeneration of FeII was enhanced by Pd/UiO-66(Zr). The hydroxyl radical could be continuously generated using only trace level FeII. 10 mg L−1 4-chlorophenol could be thoroughly degraded in the initial conditions of 75 mL min−1 H2, pH 3, 20 mM H2O2, 2 g L−1 Pd/UiO-66(Zr) and 20 μM FeII. Moreover, the removal efficiency of 15 mg L−1 sulfamethazine could be maintained at least more than 94% under the same conditions. The activity of the solid catalyst could be maintained after 6 consecutive reaction cycles. This provides new insight for improving the inherent shortcomings of the Fenton reaction, which generates large amounts of iron sludge.
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ENVIRONMENTAL TECHNOLOGY
·
2022
·
IF 3.475
Tong Li,Caixia Cheng,Kaifeng Zhang,Jie Yang,Guangshuo Han,Xiuju Wang,Zhongpeng Wang,Liguo Wang
In this paper, the hydrophilic UiO-66-NH2 nanomaterial was synthesized by the solvent-thermal method and characterized. Then, UiO-66-NH2 was introduced into the casting membrane solution of cellulose acetate (CA) forward osmosis (FO) membrane, and CA/UiO-66-NH2 forward osmosis membrane was prepared by the phase inversion method. The optimum preparation conditions of CA/UiO-66-NH2 mixed matrix membranes were determined as follows: the content of UiO-66-NH2 was 0.4 wt%, the coagulation bath temperature was 35°C, the mixing temperature was 50°C and the heat treatment temperature was 50°C. FTIR, SEM, water contact angle and AFM were carried out on CA/UiO-66-NH2 forward osmosis membrane prepared under the best preparation conditions. Compared to the CA forward osmosis membrane, the permeability and selectivity of the CA/UiO-66-NH2 membrane were improved. The water flux and reverse salt flux of the CA/UiO-66-NH2 forward osmosis membrane reached 52.32 L/(m2·h) and 2.43 g/(m2·h), respectively. The permeability selectivity of CA membranes and CA/UiO-66-NH2 membranes did not change much during 180 min, indicating that the two membranes had good long-term stability. This study shows a potential advantage of UiO-66-NH2 as additives for improvement in the desalination performance of forward osmosis membranes.
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高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2022
·Vol. 139
·期 33
·e52810
·
IF 3.057
Zhirong Hu,Jiayu Miu,Xiong-Fei Zhang,Mingmin Jia,Jianfeng Yao
UiO-66-NH 2 (Zr-based metal organic framework) is integrated into cellulose acetate (CA) to fabricate mixed matrix membranes (MMMs) through solvent-casting approach. To regulate the interfacial compatibility and suppress the non-selective voids, UiO-66-NH 2 with different particle sizes are investigated. The introduction of UiO-66-NH 2 provides additional pathways for gas molecules and renders the membrane with high CO 2 affinity, substantially augmenting the separation efficiency of UiO-66-NH 2 @CA composite membrane. By optimizing the particle size of UiO-66-NH 2 , the non-selective voids and the particle agglomeration can be effectively restricted. The optimum separation performance is obtained by U-100@CA membrane (UiO-66-NH 2 : 200 nm in size), exhibiting a CO 2 permeability of 168.8 Barrer with CO 2 /N 2 and CO 2 /CH 4 ideal selectivities of 40.2 and 51.3, respectively. The separation mechanism is ascribed to the presence of sufficient amine groups, the high CO 2 solubility of CA matrix, and superior inorganic–organic interfacial property.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2021
·
IF 4.539
Rui Duan,Hongjuan Wu,Jiahe Li,Zhaoxi Zhou,Weihua Meng,Lei Liu,Hongqiang Qu,Jianzhong Xu
Phosphor nitrile functionalized UiO-66-NH 2 /graphene (G-U-H) was prepared combined a green mechanochemical method and microwave-assisted rapid method to improve the fire safety of epoxy resin (EP). The scanning electronic microscopy, transmission electron microscope and X-ray diffraction results indicated that the G-U-H exhibited sandwich-like hybrid structure. And the -OH from graphene nanoplatelets and -NH 2 from UiO-66-NH 2 were grafted with hexachlorocyclotriphosphazene to form covalent bonds . The obtained flame retardant was added to the EP at a different content. The flame retardancy index and cure index of EP composites were calculated, and those of EP-3 were both good. The cone calorimetry test showed that the flame retardancy of EP was improved and the flame retardant mechanism is the combination of condensed phase and gas phase with the synergistic of P, N and other elements. The physical barrier of graphene nanoplatelets and the generated more stable and denser residual char in condensed phase can effectively cut off the heat and mass transmission. In gas phase, the non-flammable gases were generated to help reduce the heat released.
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Journal of the Taiwan Institute of Chemical Engineers
·
2021
·
IF 5.876
Liu Yang,Yu-Long Liu,Xian-Xian Ji,Cheng-Guo Liu,Ying Fu,Fei Ye
Background A novel luminescent sensor with dual-emitting platforms, Tb@UiO-66 , was used for highly detecting Sm 3+ and teflubenzuron. Methods Tb@UiO-66 was synthesized on basis of the exchange of guest molecules, where Tb 3+ ions were encapsulated into the cages of UiO-66 . Significant finds The results of multiband fluorescence originated from the linker-to-cluster charge transfer and the characteristic emission of Tb III . Tb@UiO-66 displayed luminescence enhancements or quenches according to small molecules. Especially for Sm 3+ and teflubenzuron, the characteristic peaks of Tb@UiO-66 at 490, 545, 585, and 621 nm increased with the increasing of the concentration of the analytes, where Tb@UiO-66 exhibited the effect of luminescence enhancement. The detection limits for detecting Sm 3+ and teflubenzuron were 0.09 μM and 0.21 μM, and the changes of luminescence intensities could be observed by naked eyes under the UV light at 365 nm. Tb@UiO-66 could also be used to detect teflubenzuron in real water samples. Tb@UiO-66 could be reused for at least 5 cycles for the detection of Sm 3+ and teflubenzuron with the framework of Tb@UiO-66 uncollapsed. These results implied that the integration of Ln III luminescent materials and Zr-MOFs by doping method provided a new strategy for fabricating novel luminescent sensors for detecting polluting small molecules.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2021
·
IF 4.539
Yawen Tan,Yi Zhou,Yuehong Deng,Haiqin Tang,Hao Zou,Yifeng Xu,Jiaxin Li
The introduction of metal-organic frameworks into semiconductor photocatalysts is one of the strategies to improve the separation efficiency of electron-hole pairs. In this study, UiO-66-NH 2 /Bi 2 WO 6 nano-heterojunction was constructed for the first time by introducing UiO-66-NH 2 into the Bi 2 WO 6 precursor solution. A series of characterizations such as XRD , XPS and FT-IR have indicated that the successful synthesis of the composites and showed that UiO-66-NH 2 and Bi 2 WO 6 are tightly connected and interacted. SEM results showed that the introduction of UiO-66-NH 2 can increase the distance between bismuth tungstate nanosheets and effectively inhibit the agglomeration of Bi 2 WO 6 . The visible light degradation efficiency of 6% UiO-66-NH 2 /Bi 2 WO 6 can reach 99.7%. The improvement of photocatalytic activity could be attributed to the formation of a type II heterojunction in the composite, which effectively promoting the separation of electron and holes.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2021
·
IF 3.764
Xu Zheng,QianLing Ma,Jianming Tan,Bo Yu
Dehumidification performance of a high-efficient compact desiccant cooling component named desiccant-coated heat exchanger (DCHE) highly depends on coated desiccant materials. Currently, mesoporous silica gels and salt-supported silica gels have been extensively studied. Silica gels have limited adsorption quantity in the middle relative pressure range, while salt-supported silica gels have potential threat of corrosion. In this work, a metal–organic framework UiO-66 that can achieve good adsorption quantity without corrosion is reported. The equilibrium adsorption test shows that UiO-66 has promising water uptake, especially in the relative pressure range of 0.35–0.65. The adsorption kinetics test displays that UiO-66 exhibits desirable dynamic water uptakes and adsorption rate constant. Dehumidification capacities of a DCHE using UiO-66 are estimated via a mathematical model and compared with silica gel- (SG) and LiCl-supported silica gel (SG/LiCl). Simulation results show that UiO-66 has better dehumidification performance than both SG- and SG/LiCl-coated samples for semiarid and semihumid climates when outdoor temperature is lower than 36 °C. Especially, when the temperature and relative pressure of inlet air are set as 30 °C and 0.35, respectively, its dehumidification capacity can be 2.7 times the amount of the SG-coated one and 1.3 times of the SG/LiCl-coated one. However, it should be more prudent in choosing UiO-66 under hot and humid climates.
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JOURNAL OF APPLIED POLYMER SCIENCE
·
2021
·Vol. 138
·期 22
·50519
·
IF 3.125
Wei Wang,Peng Zhang,Yaping Shi,Zhichao Zhang,Xin Xu,Ping Ding
The composite membrane with the advantages of high separation efficiency and wide application, has been widely concerned in the field of water purification and molecular separation. However, the common composite membrane cannot achieve continuity, or the grafting process is complex, which significantly hinders its further development. In this work, the in-situ polymerization of UiO-66/PVDF supramolecular flat membranes as the continuous and high-performance composite membrane can be easily synthesized using the supramolecular force, (such as, hydrogen bond, etc.). These supramolecular membranes exhibit good hydrophilic (61°) and anti-fouling performance for bovine serum albumin (BSA) solution with rejection rate 97.79% than the original membrane. Moreover, this membrane can achieve more MOF doping based on maintaining the membrane performance, which undoubtedly greatly improves its hydrophilicity and mechanical properties. In addition, we also characterized the porous microstructure of the UiO-66/PVDF supramolecular membrane to analyze the influence of different doping amounts on the membrane structure. This supramolecular membrane has the advantages of simple synthesis, good hydrophilicity and water separation performance, which provides a more convenient and effective way for the preparation of MOFs/polymer flat membrane, and also provides a new method and new idea for expanding the application of MOFs/polymer ultrafiltration membrane in water treatment.
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MICROCHIMICA ACTA
·
2021
·Vol. 188
·期 2
·1-11
·
IF 5.833
Li Jingxian,Jiang Ding,Shan Xueling,Wang Wenchang,Ou Guofu,Jin Haozhe,Chen Zhidong
A novel aptasensor has been fabricated based on the resonance energy transform (RET) system from MoS 2 QDs-PATP/PTCA (donor) to NH 2 -UiO-66 (acceptor). The electrochemiluminescence (ECL) signal of PTCA was greatly amplified due to the decoration of MoS 2 QDs-PATP, and the NH 2 -UiO-66 was utilized to label the signal probe DNA (pDNA), which hybridizes with the exposed aptamer anchored on the surface of MoS 2 QDs-PATP/PTCA. With the target acetamiprid, the specific binding of acetamiprid to aptamer causes the connection between the donor and the acceptor to be interrupted and produce an “on” ECL signal. Thus, an “off-on” ECL sensing platform for sensitive and selective acetamiprid assay was designed. Under the optimal condition, the ECL signal of the aptasensor was found to be linearly related to the logarithm of the acetamiprid concentration ranging from 0.1 fM to 0.1 μM with a detection limit of 0.064 fM. More importantly, the recovery rate of the ECL aptasensor was calculated to be 98.7 ~ 106% with a RSD lower 5.1% for the residual acetamiprid assay in real food samples, which indicated that the aptasensor has high potential for practical applications. Graphical abstract
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Green Energy & Environment
·
2020
·
IF 6.395
Zhuizhui Su,Bingxing Zhang,Xiuyan Cheng,Fanyu Zhang,Qiang Wan,Lifei Liu,Xiuniang Tan,Dongxing Tan,Lirong Zheng,Jianling Zhang
UiO-66-NH 2 , an important metal–organic framework, is usually synthesized by solvothermal method and the particle size is generally larger than 200 nm, which limits its catalytic applications in chemical reactions. It is very meaningful to produce UiO-66-NH 2 nanoparticles with ultra-small size, but remains challenging. Herein, we synthesized UiO-66-NH 2 nanoparticles in size of 8–15 nm that are immobilized on g-C 3 N 4 nanosheets. Compared with the UiO-66-NH 2 synthesized by the traditional solvothermal method (> 200 nm), the ultra-small UiO-66-NH 2 nanoparticles immobilized on g-C 3 N 4 have more unsaturated coordination positions and increased Lewis acidity. Owing to these combined advantages, the ultra-small UiO-66-NH 2 nanoparticles exhibit greatly improved catalytic activity for Meerwein–Ponndorf–Verley reaction than larger UiO-66-NH 2 particles.
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高影响因子
CATALYSIS LETTERS
·
2020
·Vol. 151
·期 3
·734-747
·
IF 2.482
Zhang Xiaorui,Chen Chen,Jiang Caiyun,Zhou Haifei,Cao Wang,Wang Yuping
Abstract A new type of Ag 3 PO 4 /UiO-66-NH 2 Z-scheme heterojunction nanocomposite with visible light catalytic activity was successfully prepared. The synthesis of the composite was confirmed by XRD, FT-IR, SEM, TEM, EDS, XPS. The Ag 3 PO 4 /UiO-66-NH 2 Z-scheme heterojunction can effectively improve the utilization of visible light. The optimal Ag/U/1/4 composite has the highest degradation efficiency for methylene blue (MB, 30 mg/L) in 90 min (80%) and Norfloxacin (NOR, 10 mg/L) in 150 min (85%). The decrease of Nyquist radius and the enhancement of photocurrent response indicated that the combination of photogenerated electron–hole pair in Ag 3 PO 4 /UiO-66-NH 2 composite material is significantly inhibited. N 2 adsorption–desorption and zeta potential results indicated that biggish specific surface area and negative zeta potential value are more favorable for the adsorption of the cationic dye MB. The cyclic test verified the good stability of Ag 3 PO 4 /UiO-66-NH 2 heterojunction material. Furthermore, the photocatalytic degradation mechanism of MB was discussed by introducing different traps to inhibit the possible active substances in the degradation process. This work testified that an efficient photocatalytic composite based on metal–organic frameworks can be used for the degradation of pollutants. Graphic Abstract
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JOURNAL OF HAZARDOUS MATERIALS
·
2020
·
IF 9.038
Linna Song,Tianyu Zhao,Dongzhi Yang,Xuejiao Wang,Xinmin Hao,Yaxin Liu,Shiyi Zhang,Zhong-Zhen Yu
Lightweight and wearable fabrics with rapid self-detoxification functions are highly desired to resist chemical warfare agents (CWAs). Metal organic frameworks (MOFs) with high specific surface area and customizability are singularly attractive because of their ability to effectively capture and catalytically degrade CWAs. Herein, photothermal graphene-based nanocomposite fabrics are designed by wet-spinning and chemical reduction of graphene oxide fibers followed by in situ growth of UiO-66-NH 2 . The flexible graphene fabrics decorated with UiO-66-NH 2 nanoparticles exhibit an ultrafast photothermal catalytic decontamination of dimethyl 4-nitrophenyl phosphate (DMNP), a typical simulant of CWAs. The half-life of the degradation reaction decreases from 3.4 to 1.6 min under simulated solar light irradiation, a significant gain over the values reported in the literature. Furthermore, DMNP can be degraded in 20 min by the graphene/UiO-66-NH 2 fabric, and even after 5 cycles the degradation efficiency still retains more than 92 %. More importantly, the photothermal conversion of graphene and its instantaneous heat transfer to the UiO-66-NH 2 catalyst effectively accelerate the catalytic reaction kinetics, achieving the fast detoxification of DMNP. The combination of catalytic degradation of MOFs with photothermal conversion effect of graphene makes the lightweight and flexible fabrics promising for protection against CWAs and other pollutants.
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