MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING
·
2024
·
IF 4.2
Z.H.A.O.-X.U.A.N. Jiang
In this investigation, UiO-66-NH 2 was effectively synthesized through a solvothermal approach, utilizing benzoic acid and hydrochloric acid (HCl) as modulating agents. This synthesis process intentionally introduced defects mediated by benzoic acid, and the degree of these defects was precisely adjusted by the concentration of HCl. Subsequently, the material underwent a covalent modification process through an amidation reaction, resulting in the attachment of tetrakis (4-carboxyphenyl) porphyrin (TCPP). The results demonstrated a significant improvement in the photocatalytic reduction of Cr(VI), showcasing a 125 % elevation in reduction efficiency as compared to the unmodified UiO-66-NH 2 material serving as the baseline. The performance enhancement is due to the synergistic effect of the defect structure and TCPP modification, which enhances the light absorption, promotes charge transfer and separation, reduces the recombination rate, and improves the adsorption capacity and light absorption efficiency of Cr(VI). This research introduces an innovative approach and a highly effective catalyst, offering a novel solution for modifying metal-organic frameworks (MOFs) and enhancing their photocatalytic performance in the reduction of Cr(VI).
研究领域:
材料科学
·
环境科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
·
2025
·
IF 4.7
Yanhao Xu,Ziyi Zhong,Pinle Zhang,Huancheng Huang,Kuan Cai,Xinliang Liu
Persistent organic pollutants (POPs) represent a significant environmental and health risk due to their high toxicity, persistence, strong accumulation potential, and adverse effects on human health. 4-Chlorophenol (4-CP), a type of POP, has low catalytic efficiency at low concentrations and is easily interfered with by other pollutants, making its degradation challenging. A new “recognition-enrichment-in-situ degradation” strategy is introduced to selectively remove chlorophenols from contaminated aqueous environments. In this study, ionic liquids were incorporated into the UIO-66 framework as active sites for selective adsorption. 4-CP contains phenolic hydroxyl groups and exhibits high polarity. The dispersive interactions between 4-CP and ionic liquids, along with hydrogen-bonding interactions between the Tf 2 N anion and the hydroxyl groups of 4-CP, enhance the selective enrichment of 4-CP within the nanocavities of the metal–organic frameworks (MOFs). Fe 3+ was then introduced, enabling in-situ degradation of 4-CP through photo-induced generation of free radicals and cavities from H 2 O 2 catalyzed by Fe-IL@UIO-66. The results indicated that the adsorption capacity of IL@UIO-66 for 4-CP reached 53 %, significantly higher than that for five other organic pollutants. The adsorption capacity of IL@UIO-66 for 4-CP reached 509.5 mg g −1 , 49.9 % greater than that of the original UIO-66. The degradation efficiency of 4-CP by Fe-IL@UIO-66 increased from 61 % to 81 %, and after four cycles, the material retained a catalytic activity with a degradation efficiency of 64.2 %. This study provides valuable insights into the recognition-enrichment-in-situ catalytic strategy for treating low-concentration, highly toxic wastewater.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF MEMBRANE SCIENCE
·
2018
·
IF 6.578
Xiong-Fei Zhang,Yi Feng,Zhongguo Wang,Mingmin Jia,Jianfeng Yao
Incorporating metal-organic frameworks into cellulose matrix to prepare composite membranes is promising in gas-separation applications. In this study, UiO-66-NH 2 (Zr-based MOF) nanoparticles are wrapped into the densely packed cellulose nanofibrils (CNF-COOH) via a facile vacuum filtration process. The existence of acid-base interactions and electrostatic forces between UiO-66-NH 2 and CNF-COOH renders ideal interfacial morphology. Results show that UiO-66-NH 2 is cross-linked by -COOH groups and well-dispersed in the CNF matrix. The porous UiO-66-NH 2 strengthens the diffusion process of CO 2 molecules, thus elevating the permeation flux and separation factor simultaneously. The optimum separation performance is achieved over CM-1 membrane with a CO 2 permeability of 139 Barrer and a CO 2 /N 2 selectivity ratio of 46.
研究领域:
材料科学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
WATER SCIENCE AND TECHNOLOGY
·
2024
·Vol. 89
·期 4
·873-886
·
IF 2.5
Tao Haiyan,Cao Xiaochang,Song Rujie,Zhou Zebin,Cheng Fang
A membrane-aerated biofilm reactor (MABR) combines membrane technology with biofilm processes and has unique advantages in the treatment of organic wastewater and volatile wastewater. The common membranes for MABR systems usually have relatively uneven pore structures and low bubble point pressure, resulting in unsatisfactory O 2 utilization and wastewater treatment efficiency. In this work, polydimethylsiloxane (PDMS) and UiO-66 (a Zr-based metal organic framework) were coated on the surface of a commercial polypropylene (PP) hollow fiber membrane to prepare oxygen-rich MABR membranes and modules, which showed an attractive O 2 utilization rate and wastewater treatment efficiency. The bubble points of the PDMS and PDMS-UiO-66 membranes were significantly higher than those of the PP membranes, and the PDMS-UiO-66 membranes had better oxygen enrichment capacity and biological affinity. The optimal PDMS-UiO-66 membrane modules had an O 2 permeance of 31.65 GPU (1 GPU = 3.35 × 10 −10 mol m −2 s −1 Pa −1 ), with O 2 /N 2 selectivity of 2.21. The membrane hanging effect and processing capacity for domestic sewage were greatly improved. This study may provide insights and guidelines to fabricate porous mixed matrix membranes and modules in the industry for MABR. The developed products are expected to be applied in the actual separation process. PDMS and PDMS-UiO-66 were coated on the PP support to prepare O 2 -rich MABR membranes and modules. With UiO-66 loading, the module has a higher O 2 /N 2 separation performance, a rougher and more hydrophilic membrane surface. The PDMS-UiO-66 membrane module exhibits a good biofilm hanging effect and high NH 4 + -N removal performance.
研究领域:
环境科学
·
材料科学
·
生物技术
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2018
·
IF 6.735
Shuting Zhuang,Rong Cheng,Jianlong Wang
UiO-66 type metal organic frameworks (MOFs), including UiO-66 and UiO-66-NH 2 , were synthesized, characterized, and applied for the adsorptive removal of diclofenac (DCF) from aqueous solutions. The effect of synthetic conditions (e.g., different linkers and activation temperatures) and adsorptive conditions (e.g., contact time, initial concentration, temperature, and pH) on DCF removal was examined. UiO-66-NH 2 showed a higher adsorption capacity than UiO-66, and the increase of activation temperature can improve the adsorption capacity of UiO-66-NH 2 towards DCF. The adsorption of DCF by UiO-66-NH 2 was endothermic and almost not affected by pH in the range of 4.8–7.7. The adsorption of DCF onto UiO-66 type MOFs conformed to the pseud second-order kinetic model and the Langmuir isothermal model, with adsorption capacity of 357 mg g −1 for UiO-66 and 555 mg g −1 for UiO-66-NH 2 . Electrostatic interaction and H-bonding possibly played a vital role for DCF adsorption. The as-prepared UiO-66 type MOFs were efficient adsorbent for DCF removal from aqueous solution.
研究领域:
环境科学
·
化学工程
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2024
·
IF 7.7
Ruirui Li,Wei Zhuang,Yan Gao,Yahan Bai,Keke Zhang,Zhenfu Wang
Herein, UiO-66 was selected as the immobilization carrier of Rhizomucor miehei lipase (RML). After etching and hydrophobic modification, the functionalized UIO-66 (H-UIO-66-OPA) was utilized for RML immobilization and the obtained RML@H-UIO-66-OPA showed about 70 % relative activity after incubation at 60 °C, which was much better than RML (20 %). RML@H-UIO-66-OPA was used in the synthesis of 1,3-dioleic acid glycerol (1,3-DAG) and the effects of reaction conditions (temperature, enzyme addition, substrate molar ratio, and time) on 1,3-DAG yield were investigated. Under the optimal conditions (temperature of 65 °C, enzyme addition of 2 wt%, substrate molar ratio of 2:1, and reaction time of 4 h), 1,3-DAG yield reached 77 %. Finally, Box-Behnken experimental design method was utilized to optimize the process parameters for the preparation of 1,3-DAG, and the final 1,3-DAG content was 79.80 %, which demonstrated that the model could predict the relationship between the factors and be suitable for the process optimization in 1,3-DAG preparation.
研究领域:
生物化学
·
酶工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Nanomaterials
·
2019
·Vol. 9
·期 9
·1283
·
IF 4.034
Hao Zhang,Xiaobo Shi,Jialiang Li,Parveen Kumar,Bo Liu
In this study, Zeolitic Imidazolate Framework-8 (ZIF-8)-loaded UiO-66-NH2was synthesized, characterized, and analyzed for its potential to efficiently remove dyes. The selective adsorption on ZIF-8-loaded UiO-66-NH2or its parent MOFs (UiO-66-NH2and ZIF-8) in the mixed dyes solution was explored, including anionic dye (methyl orange (MO)) and cationic dyes (methylene blue (MB) and rhodamine B (RhB)). ZIF-8-loaded UiO-66-NH2displayed much better selectivity to MB than its parent MOFs. Adsorption capacity of ZIF-8-loaded UiO-66-NH2(173 mg/g) toward MB was found to be 215% higher than UiO-66-NH2(55 mg/g). A kinetics study based on adsorption data demonstrated that the adsorption process most closely matched with the model of pseudo-second-order kinetic and Langmuir isotherm. The adsorption was an exothermic and spontaneous physical process as revealed by the values of thermodynamic parameters. Furthermore, reusability of ZIF-8-loaded UiO-66-NH2was investigated and revealed the significant regeneration efficiency in adsorption capacity for MB even after four adsorption cycles. Experimental results proved that the interaction between ZIF-8-loaded UiO-66-NH2and MB was mainly affected by the mechanism, for instance, electrostatic interaction as well as π–π stacking interactions.Keywords:ZIF-8;UiO-66-NH2composites;metal-organic frameworks;selective adsorption
研究领域:
材料科学
·
环境科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Materials Today Energy
·
2021
·
IF 7.311
Changchang Dong,Feng Wei,Jiadong Li,Qiao Lu,Xiaojun Han
The electrochemical ammonia synthesis under ambient conditions is a promising process instead of the energy-intensity Haber-Bosch process with the release of huge greenhouse gases. But it still faces sluggish catalytic kinetics owing to difficulty of N 2 adsorption and N≡N bond cleavage. Herein, the uniform ZrO 2 @C with octahedral structure is synthesized via two-step annealing treatment of UiO-66. The formation of ZrO 2 originates from Zr and O elements in UiO-66, and the grain size is confined by the produced carbon matrix from the carbonization of the organic ligand, resulting in more exposure of the active sites. ZrO 2 @C obtained at 650 °C presents excellent electrocatalytic nitrogen reduction performance with a NH 3 yield rate of 6.72 μg h −1 mg cat. −1 and a Faradaic efficiency of 2.68% at −0.6 V versus reversible hydrogen electrode (RHE). This work provides a strategy to design metal oxide@C from metal-organic frameworks for nitrogen fixation.
研究领域:
材料科学
·
电化学
·
能源化学
✓ 已验证
产品关联
DOI
高影响因子
Molecular Catalysis
·
2022
·
IF 5.089
Ji Wang,Shuqing Zhang,Yiming Han,Lilei Zhang,Qingyin Wang,Gongying Wang,Xiaoming Zhang
PET (poly(ethylene terephthalate)) is one of the most important type of thermoplastic polyesters and widely used in various fields. Titanium-based catalysts are environmentally friendly and have higher catalytic activity than antimony-based catalysts when used in industry. However, titanium-based catalysts are prone to hydrolysis and result in discolored products. UiO-66 (Zr/Ti) with different Ti 4+ contents were successfully synthesized via one-step method. The material was characterized by XRD, SEM, FT-IR, XPS, BET and TG techniques. The results demonstrates that Ti 4+ was integrated into the UiO-66 framework. NH 3 - in situ DRIFTS, pyridine-IR, and NH 3 -TPD were used to explore the acidic properties of the samples, which proved that stable Lewis acidic sites are present in the samples even at 300 °C. The catalytic performance of UiO-66 (Zr/Ti) containing different Ti 4+ was explored under different conditions. At the same time, the scale-up experiment was carried out in a 5 L reactor, and the PET chips obtained had a lower b value. The catalytic reaction mechanism of UiO-66(Zr/Ti) was demonstrated by DFT calculations and the catalytic performance was close to Sb-based catalysts.
研究领域:
材料科学
·
化学工程
·
催化
✓ 已验证
DOI
高影响因子
TALANTA
·
2020
·
IF 5.339
Bo Ruan,Jie Yang,Yi-Jie Zhang,Ning Ma,Dean Shi,Tao Jiang,Fang-Chang Tsai
The fluorescent dye molecules have gained wide attention for their applications in areas such as imaging and sensor. However, the properties of the fluorescent dyes are limited due to the built-in problems such as the aggregation-caused quenching (ACQ). Herein, a fluorescent dye@MOF was developed by encapsulating fluorescent dye molecules into the channels of metal-organic frameworks (MOFs) to disperse them. This composite material SRB@UiO-66, equipping appreciable stability, was successfully obtained with sulfonyl rhodamine B (SRB) integrated into UiO-66. The composite material overtly accelerated the fluorescence property of SRB due to the limitation of nanometer channels on SRB , while UiO-66 has some fluorescence properties. Besides, SRB@UiO-66 with dual emission centers can be utilized as ratiometric sensors for Fe 3+ detection in aqueous solution owing to their high sensitivity and selectivity. SRB@UiO-66 shows a new possibility to fabricate fluorescent molecular probes for the determination of heavy metal ions .
研究领域:
材料科学
·
分析化学
·
环境科学
✓ 已验证
DOI
高影响因子
Surfaces and Interfaces
·
2024
·
IF 5.7
Pengfei Zhu,Shuang Qin,Mengrong Geng,Heyang Cao,Zhiliang Jin,Chuanyi Wang
Photocatalytic NO removal technology is considered as one of the most effective green methods for reducing atmospheric NO but there remains the problems of lower efficiency and poor stability of photocatalysts . Rapid recombination of photogenerated electron (e − ) and holes (h + ) is known as a key issue that causes low activity and poor stability of catalysts. Herein, we report a novel AgCu@UiO-66-NH 2 photocatalyst (AgCu@UN) that is made up of AgCu alloy on the surface of Zr-MOF (UiO-66-NH 2 ) by employing in-situ photodeposition method. The experimental results of photocatalytic NO removal indicated that the optimized 0.5Ag0.5Cu@UN sample with 0.5 mg of Ag and Cu exhibited the best NO removal efficiency of 63 % for ppb-level atmospheric NO, more higher than that of pure UiO-66-NH 2 (38 %). The characterizations suggested that the excellent photocatalytic performance of 0.5Ag0.5Cu@UN can be ascribed to the efficient charge separation and transfer and the visible-light-harvesting ability due to benefiting electron migration process between AgCu alloys and UN. Moreover, the enriched electrons around AgCu could be transferred to O 2 to generate more superoxide radicals (•O 2 − ), which could oxidize NO to the final product, nitrate (NO 3 − ). The present findings can provide some novel insights for the design of efficient MOF based photocatalysts to eliminate low concentrations of NO X .
研究领域:
材料科学
·
环境科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2022
·
IF 7.968
Fei Fang,Quankun Lv,Peng Li,Yue Tao,Yan Zhang,Yi Zhou,Xuede Li,Jie Li
Defect engineering is essential for improving the adsorption performance of metal-organic frameworks (MOFs). Herein, hierarchical porous UiO-67(Zr) and analogs with controlled levels of defects were successfully obtained and applied to chemoselectively capture glyphosate (GP) from water. The obtained defective UiO-67 was stable at different pH values. The removal performance of defective UiO-67(Zr) was evaluated systematically as a function of different modulators, water chemistry and interfering ions. The maximum adsorption capacity of defective UiO-67(Zr) reached 322.58 mg/g, superior to most MOFs-based adsorbents. The defective UiO-67(Zr) also showed high selectivity for GP adsorption at high concentrations of humic acids (3 times) and interfering anions (100 times). In addition, the defective UiO-67(Zr) has shown good recovery performance and can effectively remove GP from a variety of contaminated water samples and multi-pollutant systems. The results of batch experiments and microscopic spectral characterization (XPS and FTIR) revealed that GP adsorption was mainly guided by electrostatic action, coordination, pore-filling and hydrogen bonding . These findings verified that the fabrication of defect sites played an important role in promoting the adsorption performance of MOFs. Our work provides a clue to the design of defective MOFs with high adsorption performance.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）