FIBERS AND POLYMERS
·
2023
·Vol. 24
·期 6
·1983-1994
·
IF 2.5
Feng Jiangli,Sun Hui,Yu Bin,Yang Xiaodong,Xu Lei,Liu Peng,Cui Xiaogang
A kind of NH 2 -MIL-101(Fe)@viscose spunlaced nonwoven material (VSN) was prepared by in situ solvothermal method for the adsorption of organic dyes in wastewater and then carbonized in a tube furnace under N 2 atmosphere at 300 °C to improve the adsorption performances. The results showed that the synthesized NH 2 -MIL-101(Fe) particles with a polyhedral structure were uniformly loaded on the VSN surface. After being carbonized, the NH 2 -MIL-101(Fe)@viscose spunlaced nonwoven porous carbon material (VSNC) were obtained. Compared with uncarbonized NH 2 -MIL-101(Fe)@VSN, the adsorption efficiency of NH 2 -MIL-101(Fe)@VSNC for methylene blue (MB) significantly enhanced and could reach 98.3% under the condition of water bath temperature of 30 °C and pH 9. According to adsorption thermodynamic analysis, the MB adsorption process by NH 2 -MIL-101(Fe)@VSNC was spontaneous. The quasi-secondary adsorption kinetic model was more suitable to describe the whole adsorption process of NH 2 -MIL-101(Fe)@VSNC, implying that the adsorption mechanism of NH 2 -MIL-101(Fe)@VSNC for MB was mainly chemical adsorption. NH 2 -MIL-101(Fe)@VSNC presented good structure stability and reusability during the adsorption process. After being recycled five times, the MB adsorption efficiency still maintained about 86.3%.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2023
·
IF 6.2
Hao Tu,Huihu Wang,Huang Xu,Ziguan Zhang,Guode Chen,Chenhuinan Wei,Xing Xiang,Zhixiong Xie
In this work, a series of ZnIn 2 S 4 nanosheets encapsulated NH 2 -MIL-125(Ti) heterostructures (NM-125(Ti)@ZIS) have been rationally designed and established through a facile oil bath method. The photocatalytic Cr(VI) reduction and H 2 evolution performance on NM-125(Ti)@ZIS were elaborately modulated by adjusting the mass ratio of two components, introducing S vacancy and loading cocatalysts. The experimental results demonstrate that the optimized NM-125(Ti)@ZIS heterostructure with mass ratio 3:1 of NM-125(Ti) to ZIS has an excellent Cr(VI) reduction performance in neutral solution, giving 98% reduction efficiency within 60 min. Moreover, the NM-125(Ti)@ZIS heterostructure, following the introduction of sulfur vacancies and the incorporation of Pt nanoclusters , demonstrates an optimal visible light (λ > 420 nm) hydrogen evolution rate of 4.708 mmol/g/h, which is 5.82 times greater than that of pristine ZIS. A thorough investigation of the microstructures and photoelectrochemical properties of the NM-125(Ti)@ZIS heterostructures reveals that the intimate contact interface, sulfur vacancy, and Pt nanocluster serve to effectively enhance charge separation efficiency, thereby improving the photocatalytic performance. Further analysis on the charges behavior at the interface verifies that a novel Z-scheme heterojunction has been constructed between ZnIn 2 S 4 and NH 2 -MIL-125(Ti).
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RSC Advances
·
2021
·Vol. 11
·期 62
·38982-38989
·
IF 3.361
Zang Chuanfeng,Han Xiangye,Dong Erying,Shen Feiyu,Yan Tingting,Wang Runyue,Zhang GuangyuYu
A new type of nanofiber membrane was prepared by mixed electrospinning of cellulose diacetate and amino-terminated hyperbranched polymer (HBP-NH2), and glutaraldehyde (GA) crosslinking was used to improve its water resistance and shape retention. pH, adsorption time, and initial solution concentration on Cu(II) and Cr(VI) ions were studied. Results showed that the prepared GA-CDA/HBP-NH2 nanofiber had good spinning uniformity, hydrophilicity, and adsorption effect on Cu(II) and Cr(VI) ions compared with the pure CDA nanofiber. The maximum adsorption capacity of GA-CDA/HBP-NH2 for Cu(II) and Cr(VI) was 50.2 and 176.6 mg g−1, respectively.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2026
·
IF 5.4
Yao Zhang,Jiefang Feng,Juan Yang,Feiyang Chen,Yunjia Liu,Xiaoxian Hu,Lijin Huang,Nianjun Yang
Detecting trace nitrofurantoin (NFT) residues in food and water is critical for public health, yet practical applications are constrained by the scarcity of highly sensitive sensing materials. Herein, an MXene/amino-functionalized carbon nanotubes (NH 2 -CNTs) hybrid composite was fabricated via a facile electrostatic self-assembly strategy for NFT sensing. In this design, the positively charged NH 2 -CNTs spontaneously assemble with negatively charged MXene nanosheets through strong electrostatic interactions, serving simultaneously as interlayer spacers to effectively prevent MXene restacking and as highly conductive bridges with excellent electrocatalytic activity. This synergistic assembly yields a three-dimensional interconnected conductive network, which endows the composite with significantly enhanced electron-transfer kinetics, enlarged electrochemically active surface area, and superior electrocatalytic activity, thereby enabling pronounced signal amplification. Consequently, the optimized sensor with a mass ratio of 5:1 delivered excellent analytical performance toward NFT, with an ultrahigh sensitivity of 22.11 μA μM −1 cm −2 , a linear detection range of 0.05–15 μM, and a detection limit of 17 nM. Moreover, the sensor was successfully applied to the quantitative determination of NFT in milk, environmental water and honey samples, affording recoveries of 94.7–107.5%. These findings provide a facile strategy to overcome MXene restacking and highlight the promising potential of this sensing platform for food safety and environmental monitoring. Download: Download high-res image (148KB) Download: Download full-size image
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2023
·
IF 4.2
Wei Zhang,Runtang Liu,Longwen Lei,Binbin Nian,Shipin Yang,Yi Hu
Efficient and stable catalysis has always been a fundamental concept in enzyme-catalyzed industrial processes. However, the poor stability of laccase has hindered its application in industry. The conventional methods of immobilization have proven to be ineffective in achieving both stability enhancement and the maintenance of high activity simultaneously. To address this challenge, we have constructed a magnetic core–shell structured metal–organic framework doped with copper ions (MCIL@Cu-UiO-66-NH2), which leverage the synergistic effects of copper ion activation and covalently binding to immobilize laccase. The resulting immobilized laccase exhibited high activity recovery (89%) and stability, retaining 90% relative activity after 30 days of storage and 66% of its initial activity after being exposed to a temperature of 60 °C for 6 h. The application of immobilized laccase in the removal of aqueous organic pollutants was also investigated. The results demonstrate that immobilized laccase can remove 2,4-dichlorophenol completely within 8 h and maintains approximately 90% removal efficiency after undergoing five cycles. Moreover, immobilized laccase also exhibited favorable results in the removal of other phenolic pollutants and typical aromatic pollutants, which are difficult to degrade, such as indole and anthracene. The copper ion-doped magnetic MOF composite novel introduced in this work demonstrated promising potential as an efficient carrier for laccase immobilization, and the immobilized laccase exhibits practical application prospects in the field of wastewater treatment.
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Journal of Environmental Chemical Engineering
·
2023
·
IF 7.7
Baiyu Chen,Man Zhang,Kaili Yao,Churu Zhang,Qi Wu,Tianding Hu,Shaoyun Shan
Metal-organic frameworks (MOFs) have attracted exciting application prospects in photocatalytic hydrogen (H 2 ) evolution due to the diversity of organic ligands and metal ions . However, the inappropriate conduction band position of pristine MOFs and corresponding large overpotential for H 2 evolution restrict the H 2 production under visible light. Herein, a dye-sensitized NH 2 -UiO-66 anchored with copper ions (EY-6Cu-NU-66) was synthesized by in-situ Cu anchoring followed by Eosin Y sensitization. The H 2 production activity showed that EY-6Cu-NU-66 reached 3579.82 μmol·g −1 ·h −1 under visible light, which was four times higher than that of dye-sensitized pristine NU-66 (EY-NU-66) and 99-fold higher than that of 6Cu-NU-66 free of dye sensitization. A series of characterizations and theoretical computations indicated that photo-generated electrons first transfer from the excited Eosin Y to the lowest unoccupied molecular orbital (LUMO) of the NU-66, then further transfer to the transition Cu II /Cu I metal center that is formed by Cu anchored on -NH 2 . This tandem mechanism not only improves the visible-light absorption ability of NU-66 but also promotes its separation efficiency of photo-generated carriers, thus greatly reducing the overpotential for H 2 evolution. This work provides a new strategy for visible-light-driven H 2 production by dye-sensitized MOF-based materials without noble metal loading.
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Journal of Environmental Chemical Engineering
·
2023
·
IF 7.7
Yongtong Lei,Lijing Zhu,Jilong Xu,Shuan Liu,Zhixiang Zeng,Xiaocheng Li,Gang Wang
Metal organic framework (MOF) with fine pore structures, ultra-high porosity and large specific surface area can provide more water transport channels while achieving precise sieving of different sizes of ions, which is a promising material for high efficiency desalination. However, particle agglomeration, interface incompatibilities and interface defects severely restrict the performance of MOF-based membranes. It is still a challenge to construct MOF-based desalination membranes with both high water permeability and high ion sieving. Herein, the UiO-66-NH 2 based nanofiltration membrane was fabricated by in-situ growth of UiO-66-NH 2 on Nylon membrane and composed with polyamide (PA) layer by interfacial polymerization (IP). With 12 h solvothermal reaction, the UiO-66-NH 2 nanoparticles are found uniformly loaded on the Nylon substrate. Therefore, the water molecule transport channels provided by UiO-66-NH 2 nanoparticles reduce the transport resistance, which can improve the water permeability. More importantly, UiO-66-NH 2 nanoparticles are found to be involved in the IP process, which can reduce the interfacial defects and thus enhance the bonding force between the PA layer and base film. The synergistic effect of the UiO-66-NH 2 and PA layer improves the nanofiltration performance of the membrane with rejection rate of 92.97% for Na 2 SO 4 and the pure water permeance (PWP) of 11.55 L m −2 h −1 bar −1 . The N-UN12 @PA membrane also has excellent antifouling performance (flux recovery ratio (FRR) of 95.86%, reversible fouling ratio (Rr) of 33.93%, irreversible fouling ratio (Rir) of 4.14%). Unlike the mixed-matrix membrane (MMM) and polycrystalline MOF membrane, this strategy provides a promising method to prepare high-performance nanofiltration membrane for desalination.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2023
·
IF 5.2
Nian Li,Zi-jian He,Jia-hui Zhao,Zhi-dong Zhao,Xing-rui Qi,Hao-dong Wang,Bo Liu,Hua-jie Lai,Tao Jin
Developing magnetic adsorbent that combines the merits of quick response, excellent enrichment capacity, uniform and stable dispersivity is of paramount importance in pollutants pretreatment. In this work, tunable strawberry-like Fe 3 O 4 @SiO 2 -NH 2 @Au@ 2-ME magnetic solid phase extraction materials were prepared via assembly method. The obtained nanocomposites were characterized using scanning electron microscopy, X-ray diffraction spectroscopy, infrared spectroscopy , X-ray photoelectron spectroscopy, and whereafter the preparation method was optimized. Integrating magnetic solid-phase extraction with high-performance liquid chromatography and fluorescence detection , a comprehensive enrichment and detection method toward bisphenol A (BPA) was well established. This method demonstrated high efficiency and rapidity, achieving rapid enrichment of BPA. The as-developed method exhibited good linear correlation within the range of 10.0–500 μg·L −1 , with a recovery of 85–92%. It showed excellent sensitivity and reproducibility in BPA extraction with low limit of detection (LOD, 0.274 μg·L −1 ), limit of quantitation (LOQ, 0.913 μg·L −1 ) and relative standard deviation (RSD, 1.5%, n = 6), respectively. The proposed Fe 3 O 4 @SiO 2 -NH 2 @Au nanoplatform firmly supports the envision that proper surface functionalization of magnetic substrate could promote the enrichment capacity toward various pollutants in actual application scenarios.
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Journal of Environmental Chemical Engineering
·
2020
·
IF 4.3
Yi Cheng,Jilin Zhang
Excessive phosphate in wastewater can cause eutrophication of water body, which will worsen the ecological environment and threaten human health and biological life safety. Adsorption of phosphate is the most effective way to remove phosphate, and efficient adsorbent is the key. Amorphous La(OH) 3 has been deemed as a potential phosphate adsorbent on account of high adsorption capacity and environmentally friendly property. However, it also shows some disadvantages such as easy agglomeration, poor water dispersion. In this study, UiO-66-NH 2 was used as carrier to load amorphous lanthanum hydroxide as an adsorbent for phosphate removal. The adsorbent (UiO-66-NH 2 @La(OH) 3 , ULCs) has good water dispersibility and it is easy to be separated and recovered. At the same time, the maximum phosphate adsorption capacity can reach 140.7 mg P/g. The adsorption process accords with pseudo second order kinetic model and Freundlich isotherm model. The thermodynamic results showed that the adsorption process was spontaneous and endothermic. In addition, in the presence of coexisting anions (such as Cl − , SO 4 2− , NO 3 − ), it also exhibited high selectivity and phosphate removal efficiency. Meanwhile, the adsorption capacity keeps at a high level in the range of pH 3–11. By the merit of above-mentioned properties, the prepared material is expected to be an ideal candidate for phosphate removal from contaminated water.
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Catalysts
·
2020
·Vol. 11
·期 1
·24
·
IF 3.52
Juan Du,Jiaxin Zhang,Tingyu Yang,Renming Liu,Zhiyi Li,Dandan Wang,Tong Zhou,Yucun Liu,Chunbo Liu,Guangbo Che
The BiOI/NH2-MIL-125(Ti) composite photocatalyst with excellent photocatalytic performance was prepared by the solvothermal method. For the BiOI/NH2-MIL-125(Ti) (BNMT) system, the contents of NH2-MIL-125(Ti) in BNMT-4, BNMT-5, BNMT-7, BNMT-9, and BNMT-10 were 4 wt %, 5 wt %, 7 wt %, 9 wt %, and 10 wt %, respectively. XRD, XPS, SEM, and TEM characterizations indicated that BiOI/NH2-MIL-125(Ti) was successfully prepared. Brunauer, Emmett, and Teller (BET) and UV–vis diffuse reflectance spectra photoelectrochemical analysis indicated that BNMT-9 can make the specific surface area and photo absorption region larger than BiOI. In addition, the separation efficiency of photogenerated carriers was improved, and the recombination efficiency was reduced. The degradation percentages of Rhodamine B (RhB) and p-chlorophenol (P-CP) reached 99% and 90% over BNMT-9 under visible light irradiation. Additionally, the catalysts had high stability. The results of the active spices trapping experiments test indicated that h+was the main active species. The possible degradation mechanism was proposed.Keywords:photocatalysis;BiOI;NH2-MIL-125(Ti);organic pollutants
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2020
·
IF 3.232
Chunhua Lin,Zhifeng Zou,Zhiwei Lei,Li Wang,Yonghai Song
Ellagic acid (EA) is a symmetric natural phenol bioactive compound present in fruits and nuts, and has attracted substantial interest worldwide owing to its beneficial health effects. Here, the exploration of luminescent metal-organic frameworks (MOFs) of MIL-101(Al)-NH 2 (MIL = Materials of Institute Lavoisier) for rapid and sensitive sensing of EA in aqueous solution was reported initially. The porous MIL-101(Al)-NH 2 MOFs was synthesized by solvent-thermal method with inexpensive 2-aminoterephthalic acid and aluminum salt, which exhibited uniform spherical crystals (~340 nm) and specific mesoporous structure (3.2 nm). The fluorescence intensity of MIL-101(Al)-NH 2 at 425 nm showed a good linear relationship with EA concentration in the range of 0.15–100 μM. The detection limit was as low as 43.8 nM, the rapid response time was within 2 min, and the cost of detection was low. In addition, the “turn off” fluorescence probe could be utilized for visual detection of EA according to the color change under the UV lamp. Based on the Stern-Volmer equation, the quenching constants was decreased with the rise of temperature, which indicated that the probable quenching mechanism was static quenching. The nanoprobe was successfully used to detect EA in the cherry and serum samples. MIL-101(Al)-NH 2 represents the first instance of MOFs-based fluorescent probe in EA detection. This work not only enriches the detection method of EA, but also expands the potential application of MIL MOFs in small molecules.
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Arabian Journal of Chemistry
·
2020
·
IF 4.762
Zhen Huang,Chen Wang,Jiling Zhao,Shixing Wang,Yang Zhou,Libo Zhang
A new adsorbent was successfully fabricated by chemically linking pyromellitic acid onto a zirconium-based metal-organic framework composite for selective adsorption of Pd(II) from an aqueous solution. The adsorbent was characterized by Fourier transform infrared spectroscopy, Brunauer–Emmett–Teller equation and scanning electron microscope. The adsorption capacity, selectivity and repeatability of the adsorbent were tested by batch experiments. The optimum pH was 2.0, and the maximum adsorption capacity at room temperature was 226.1 mg/g. In the kinetic experiments, the adsorption process achieved equilibrium within 5 h and generally conformed to the quasi-second kinetics and Freundlich isotherm model. The N-H and O H groups on the adsorbent interacted with Pd(II) by electrostatic and coordination action. The adsorbent maintained excellent adsorption capacity after at least 5 cycles. At the same time, the selectivity of the adsorbent in aqueous solution is excellent from interfering ions. Therefore, the new adsorbent will have an obvious application prospect on the recovery of palladium.
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