JOURNAL OF MOLECULAR LIQUIDS
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2023
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IF 6
Guohao Cheng,Xing Li,Zhao Li,Kaixin Zhao,Guifen Zhu
Benzydamine hydrochloride (BDH) is a kind of nonsteroidal anti-inflammatory drugs for the treatment of inflammation. However, research on removing BDH from the environment has not attracted attention. Herein, a green deep eutectic solvent (DES) as functional monomer and magnetic metal organic frameworks (MUiO-66-NH 2 ) as supporter help to form more effective recognition sites and easy separation properties in polymerization procedure of the surface imprinted polymer (DES-MMIP). The performance of novel DES-MMIP for the selective removal of the template (BDH) in water was characterized and evaluated. The equilibrium experiment results showed that the maximum adsorption capacity of BDH can reach 41.18 mg g −1 , and fast adsorption equilibrium was obtained within 30 min. Due to the participation of magnetic MUiO-66-NH 2 and DES, the prepared DES-MMIP had excellent separability, and the adsorption capacity towards template (BDH) was 1.4–2.6 times that of other commercial adsorbents (PS-DVB, HLB, silica and zeolite). The DES-MMIP combined with UV-via was successfully applied to remove BDH from eight environmental samples. Additionally, the DES-MMIP adsorbent can be reused 5 times and still maintain excellent recovery. This work provides a promising method for preparing an efficient adsorbent for the fast separation and selective removal of BDH in the environmental field.
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DESALINATION
·
2022
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IF 11.211
Lifeng Yao,Shengzu Zhang,Ruobing Wang,Lei Zhang,Yi Wang,Weiyan Yin
Efficient treatment of complex rare earth (RE) smelting wastewater has drawn great attention due to its potential environmental toxicity and the high demand of RE in modern technologies . However, it is still a challenge to achieve the simultaneous recovering RE and separating oil from wastewater. This study makes the first attempt to fabricate a versatile membrane, namely H-UiO-66-PF2, by loading 2-hydroxyphosphono acetic acid functionalized UiO-66 on polyester fabric through one-pot reaction strategy, and reports for the first time the simultaneous separation of oil/water mixtures and recovery of Gd(III). The H-UiO-66-PF2 exhibits standout oil/water separation performance with water flux up to 126,300 L·m −2 ·h −1 and separation efficiency above 99.8 %. Besides, the maximum adsorption capacity of H-UiO-66-PF2 for Gd(III) is reached 156.5 mg/g, adsorption equilibrium time is within 60 min. Moreover, the H-UiO-66-PF2 possesses high stability and recyclability , even after 20 cycles, separation efficiency and flux are 98.9 % and 105,200 L·m −2 ·h −1 , respectively. Most notably, in addition to the separation of oil/water emulsion, complete Gd(III) capture is achieved from wastewater through filtration process . Therefore, this work provides a new design strategy to fabricate the composite membrane with great prospects for sophisticated smelting wastewater cleanup.
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JOURNAL OF ELECTRONIC MATERIALS
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2022
·Vol. 51
·期 11
·6121-6133
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IF 2.047
Mou Jiaxin,Xu Yunlan,Zhong Dengjie,Chang Haixing,Xu Chunzi,Wang Hui,Shen Hongyu
In order to enhance the photoelectric conversion efficiency of a photoanode and broaden its light absorption range, a ZnIn 2 S 4 /UiO-66/TiO 2 /Ti composite photoanode was developed. The maximum photocurrent density of the prepared photoanode is 2.56 mA cm −2 at 1.2 V (versus SCE), which is 1.79 times higher than that of ZnIn 2 S 4 /TiO 2 /Ti. The rhodamine B (RhB) removal rate, short-circuit current density and maximum power density of a photocatalytic fuel cell (PFC) constructed with the ZnIn 2 S 4 /UiO-66/TiO 2 /Ti photoanode and a Cu cathode are 98.01%, 0.22 mA cm −2 and 16.97 μW cm −2 respectively. The enhancement of the PFC performance is mainly attributed to the extremely good energy band matching and nano-size interface contact between ZnIn 2 S 4 and UiO-66. The existence of UiO-66 can be as an electronic transmission bridge, which not only facilitates the rapid transfer and utilization of photogenerated electrons, but also improves the adsorption ability of the photoanode for RhB molecules. Graphical Abstract
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CHEMICAL ENGINEERING JOURNAL
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2022
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IF 16.744
Rui Ji,Zhuzhu Zhang,Lechen Tian,Liujun Jin,Qingfeng Xu,Jianmei Lu
A novel BiOI-incorporated NH 2 -UiO-66 composite photocatalyst, NH 2 -UiO-66@BiOI, was prepared using an in-situ successive ion-insertion method. The in situ grown BiOI nanosheets exhibited an ultrathin structure and were uniformly dispersed on NH 2 -UiO-66. The formation of tight heterojunctions, characteristics of enhanced visible light absorption and availability of abundant exposed active sites facilitated the efficient activation of peroxymonosulfate and the rapid degradation of Bisphenol A in water (12 min). Surprisingly, the photocatalyst maintained a fast degradation rate of Bisphenol A under the interference of different conditions. The research explored the charge transfer pathways and radical species between the heterojunction components, indicating that the heterojunction type of the NH 2 -UiO-66@BiOI was Z-scheme. In addition, the degraded intermediate components and high mineralization rate indicated that Bisphenol A was deeply degraded. In conclusion, this study synthesized metal–organic framework-based photocatalysts through a simple preparation method, which has potential application value in the rapid degradation of bisphenol A.
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CHEMICAL ENGINEERING JOURNAL
·
2022
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IF 16.744
Tianyu Wang,Chen Zhao,Linghui Meng,Yujia Li,Hongyu Chu,Fei Wang,Yingru Tao,Wen Liu,Chong-Chen Wang
Sulfadiazine (SDZ), as a broad-spectrum pharmaceutical antibiotic, has drawn extensive attention owing to its wide application and persistence. Photocatalytic oxidation has been considered as a high-efficiency and environment-friendly technology for degrading organic contaminants. A novel BiOI/UiO-66 p-n heterojunction (BiU- x ) was fabricated via the in-situ deposition of p-type BiOI nanoplates on n-type UiO-66 octahedrons with the aid of a controlled precipitation method. The optimizing BiU-9 heterojunction exhibited a remarkably enhanced photocatalytic efficiency in removing SDZ, in which the SDZ (5 mg/L) removal efficiency over BiU-9 (0.5 g/L) reached nearly 100 % within 90 min of visible light irradiation. The influence of some important environmental factors (e.g., photocatalyst dosage, pH, co-existing inorganic anions and real sunlight irradiation) were systematically investigated. Such improvement mechanism should be assigned to the following three factors. Firstly, the introduction of narrow gap semiconductor BiOI effectively improved photo adsorption capacity. Secondly, benefiting by the large specific surface area, the involvement of UiO-66 contributed to boost the surface active sites. Most importantly, an internal electric field at the contact interface between UiO-66 and BiOI accelerated the separation of photo-generated electrons and holes. Furthermore, · O 2 − and photo-generated holes were identified as the dominating reactive species accounting for the SDZ removal. The decomposition pathways of SDZ and ecotoxicities of the intermediates were analyzed via combing with LC-MS/MS and T.E.S.T theoretical calculation. This work may provide an alternative way for enhanced photocatalytic performance of MOF-based materials through construction of p-n heterojunction with bismuth-based semiconductors.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2022
·
IF 9.965
Jiahao Liu,Liguo Shen,Hongjun Lin,Zhengyi Huang,Huachang Hong,Cheng Chen
Metal-organic frameworks (MOFs) have been considered as promising nanofillers to fabricate mixed matrix membranes for water treatment. However, manipulating distribution of MOFs nanoparticles in the membrane matrix remains a great challenge. In this study, UiO-66 was firstly coated by magnetic Ni via an in-situ reduction reaction, and then incorporated into polyethersulfone (PES) membrane matrix to prepare PES-Ni@UiO-66 membrane. The magnetic Ni allowed to manipulate the distribution of magnetic Ni@UiO-66 in the phase-inversion process by an external magnetic field. The hydrophilic Ni@UiO-66 can be pulled onto membrane surface by the magnetic force, endowing the prepared membrane with rather higher hydrophilicity. The prepared membrane exhibited superior water permeability with a pure water flux of 611.5 ± 19.8 L·m −2 ·h −1 and improved antifouling performance. Moreover, benifiting from photocatalytic activity of the exposed Ni@UiO-66 on membrane surface, the obtained PES-Ni@UiO-66 membrane demonstrated excellent photocatalytic self-cleaning ability with a flux recovery rate (FRR) higher than 95% under UV irradiation. Analyzing by extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) theory indicated that the improved antifouling performance could be attributed to less attractive or even repulsive interaction between the prepared membrane and pollutants. This work provided valuable guidance for structural regulation and development of high-performance MOFs-based membranes for water treatment.
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ACS Applied Materials & Interfaces
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2022
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IF 10.383
Chuan Zhou,Bo Yuan,Shouxin Zhang,Guang Yang,Lin Lu,Heguo Li,Cheng-an Tao
Zirconium-based metal–organic frameworks (Zr-MOFs) have been considered as prospective materials for the degradation of nerve chemical warfare agents (CWAs) but show poor catalytic performance toward blister agents. Moreover, the powder issues and the poor adsorption capability also remain as the major challenges for the application of Zr-MOFs in practical CWA detoxification. Herein, a series of defected granular UiO-66-NH2 metal–organic gels are synthesized via adjusting the amount of added concentrated hydrochloric acid for the decontamination of 2-chloroethyl ethyl sulfide (2-CEES), a sulfur mustard simulant. The half-life of 2-CEES decontaminated by defected granular UiO-66-NH2 metal–organic gels can be shortened to 7.6 min, which is the highest reported value for MOFs under ambient conditions. The mechanism of decontamination is that the amino group on the linkers in UiO-66-NH2 MOGs undergoes a substitution reaction with 2-CEES to yield 2-(2-(ethylthio)ethylamino)terephthalic acid, which is less toxic and fixed in the frameworks. The recycling test corroborates that the granular UiO-66-NH2 xerogels possess good stability and reusability. Static adsorption and desorption tests show that UiO-66-NH2 xerogels possess a high 2-CEES vapor adsorption capacity of 802 mg/g after exposure for 1 d and only 28 wt % desorption capacity after air exposure for 7 d. The dual function of ultrafast degradation and high adsorption capability provide a firm foundation for using UiO-66-NH2 xerogels as a future protection media.
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APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Zhen-Peng Cui,Le-Xi Zhang,Heng Xu,Yan-Yan Yin,Bo Tang,Li-Jian Bie
Metal-organic frameworks (MOFs) have been proved to be outstanding candidates for humidity sensors, however, pure MOFs are still limited in hysteresis, integration, and intelligence. In this investigation, inspired by a single-site-ion strategy for catalysis, UiO-66-NH 2 is first grafted by 2, 6-DPA (2, 6-dipicolinic acid) molecules (named as U-DPA) and then combined by Zn (II) ions (noted as U-DPA-Zn). Taking advantage of electrolyte and MOF, U-DPA-Zn exhibits significantly enhanced humidity sensing performance than UiO-66-NH 2 and U-DPA. U-DPA-Zn possesses the highest sensitivity (S r = 8.07 × 10 3 ), the best linearity (R 2 = 0.994), the shortest response-recovery time (τ res = 2 s, τ rec = 105 s), the smallest hysteresis (ΔH = 1.81%), as well as good repeatability in a wide relative humidity (RH) range (11%-97%). Thanks to its excellent properties, U-DPA-Zn shows great potential in the field of monitoring human respiration (breath detection) and water evaporation on human skin (finger detection). Additionally, the humidity sensing mechanism is discussed based on complex impedance analysis, revealing the single Zn (II) make giant contribution to MOFs. This work provides an optional material for humidity sensors and further a new strategy to improve the humidity sensitivity of pure MOFs.
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JOURNAL OF CATALYSIS
·
2022
·
IF 8.047
Chunhua Wang,Xiang Li,Ying-Ya Liu,Anjie Wang,Qiang Sheng,Chen-Xi Zhang
The hydrodesulfurization (HDS) of dibenzothiophene (DBT) was studied over a series of Pd catalysts supported on Zr-based metal-organic frameworks, UiO-66 and its amino-functionalized analogues (UiO-66-xNH 2 , where x represents the molar ratio of 2-amino-1,4-benzenedicarboxylic acid/1,4-benzenedicarboxylic acid) to gain an insight into metal-support interactions. Pd/UiO-66 behaved better than a Pd/γ-Al 2 O 3 catalyst and a Pd/MCM-41 catalyst. The presence of amino groups showed minor negative influence on the conversion of DBT but significantly affected the activities and selectivities of different reaction pathways. With the increase in the content of amino groups, the direct desulfurization (DDS) pathway activity of the Pd/UiO-66-xNH 2 catalysts increased, while their hydrogenation pathway activity decreased. This provides an approach for the regulation of the pathway selectivities of Pd HDS catalysts. Based on kinetic analysis and characterization results, we propose that the amino groups affect the HDS performance of Pd/UiO-66 mainly by affecting the adsorption of reacting molecules on metal particles.
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DESALINATION
·
2023
·
IF 9.9
Chuqing Cao,Fengnan Liu,Fangqing Li,Onyeagoro Robinson Uzochukwu,Lin Chen
Membrane distillation (MD) is a promising desalination technology that combines traditional distillation processes with membrane separation technology , but when the feed solution contains amphiphilic substances such as surfactant, the hydrophobic membrane is prone to being wetting, which hinders its widespread application. In this study, a novel Janus membrane was developed by embedding Zr-MOF and silver nanowires into the modified graphene oxide composite membrane to improve its separation performance, and the effect of high-concentration SDS on the membrane performance was studied. The experimental results showed that the conductive membrane exhibited excellent performance when powered on for 5 min every 2.5 h under 2 V voltage. The flux stabilized at 19.6 L/(m 2 h) with a desalination rate up to 99.9 % and no obvious signs of membrane wetting. It was found that the effect of electric field caused a negative charge on the membrane surface , forming a charge repulsion force with the SDS. Simultaneously, intermittent electrical flotation can effectively remove SDS that has accumulated on the membrane surface, thus achieving efficient and stable operation of MD system. Moreover, a machine learning approach with Catboost was applied to predict and unveil the complex effects on membrane performance, providing a deep insight to treat wastewater containing surfactant.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2023
·
IF 8.2
Lili Zhang,Yuefeng Huang,Jiaqing Zhang,Enqing Zhu,Jinxia Ma,Zhiguo Wang
A combination of multiple methods can greatly intensify the removal efficiency of hazardous substances. Herein, the synergistic utilization of adsorption and catalysis achieved for the highly efficient removal of hexavalent chromium (Cr 6+ ). A paper-based palladium nanoparticles/UiO-66-NH 2 (PdNPs/UiO-66-NH 2 /LP) composite catalyst was prepared using lignocellulose paper-based material (LP) for the loading of UiO-66-NH 2 MOFs materials, with the lignin in LP as the reducer for the in-situ synthesis of PdNPs (12.3 nm) on UiO-66-NH 2 MOF materials. Lignocellulose paper-based materials with high strength (82 N·m/g) realized low-cost and environmentally friendly preparation and guaranteed the practicability of PdNPs/UiO-66-NH 2 /LP composite catalyst. The prepared PdNPs/UiO-66-NH 2 /LP achieved high-efficiency catalytic activity for hazardous Cr 6+ removal through a constructed adsorption-catalytic synergistic system, in which the removal efficiency of Cr 6+ in 10 min was increased by 2 times compared with a composite catalyst without MOFs loading. Finally, the PdNPs/UiO-66-NH 2 /LP composite catalyst demonstrated the great efficiency and practicality of water pollution treatment through synergistic adsorption enrichment and catalytic reduction.
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高影响因子
ANALYTICA CHIMICA ACTA
·
2023
·
IF 6.2
Qing Yang,Chenghui Li,Jing Hu,Xiandeng Hou
Background Selenium is an indispensable microelement for humans and food is the main source of selenium intake. As one of the best techniques for the determination of selenium, inductive coupling plasma-mass spectrometry (ICP-MS) features some unique advantages, such as wide linear range and high sensitivity. Nevertheless, it still remains a challenge to achieve the accurate and high sensitivity determination of ultra-trace selenium in food samples by ICP-MS owning to the high first ionization energy of selenium and interferences from sample matrices as well as isobaric interferences. Results In this work, UiO-66-NH 2 (metal organic framework, MOF) was fast synthesized by microwave method and employed for the preconcentration of ultra-trace selenium with an adsorption efficiency of nearly 100 %. The selenium-adsorbed MOF was collected by filtration, and then simply converted to slurry for in situ hydride generation (HG) for sensitive detection of selenium by ICP-MS. Various factors affecting the adsorption of selenium by the MOF (including pH, adsorption time, and amount of MOF) together with main parameters of hydride generation (including concentrations of HCl and NaBH 4 ) were carefully evaluated. Experimental results show that effective matrix separation can greatly reduce interference, with an excellent detection limit of 1 ng/L. The practicability and accuracy of this method were successfully confirmed by the determination of trace selenium in several food samples. Significance UiO-66-NH 2 (MOF) was used as an effective adsorbent for the preconcentration of selenium prior to direct slurry sampling HG-ICP-MS determination. Direct slurry sampling avoided additional elution procedures and was conducive to eliminating matrix and isobaric interferences. High sensitivity and interference-free determination were achieved for determination of ultra-trace Se in complex food samples.
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