Journal of Cleaner Production
·
2022
·
IF 11.072
Mingjun Xu,Qian Zhang,Ziqi Zhu,Yuwei Xue,Ting Zhang,Junming Hong
Prussian blue analogs (PBAs) have been widely explored as catalyst for peroxymonosulfate (PMS) activation. However, the drawbacks of poor electron transfer ability and degradation performance of PBAs hinder their practical application. In this study, oxygen vacancy (OV)-rich Mn-Fe PBA was regulated through phosphoric acid and ammonia water chemical etching to overcome these drawbacks. Experimental and theoretical investigations indicated that the regulation of OVs was favorable for more Fe 2+ and Mn 3+ active sites exposure and higher specific surface area to facilitate PMS activation. Sulfate radical (SO 4 •− ), hydroxyl radical (HO•), and single oxygen ( 1 O 2 ) were verified as main reactive species for PMS activation during catalytic reaction . Density functional theory calculation results showed that the OV-rich NOE-PC-300 had the highest pollutants degradation capability, with complete degradation of bisphenol A (BPA) and acetaminophen (APAP) within 40 min. Through regulation of OVs by chemical etching, highlighted adsorption ability and elongated O–O bond of PMS were obtained. This research showed that NOE-PC-300 is an efficient and harmless catalyst for activating PMS, and it has immense application potential in practical wastewater treatment .
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2022
·
IF 10.319
Lu Zhang,Jianhao Qiu,Guanglu Xia,Dingliang Dai,Xiang Zhong,Jianfeng Yao
Photocatalytic oxidation of aromatic alcohol into aromatic aldehyde using O 2 has received huge attention, while the reaction that occurred in ambient air is rarely studied but follows the green-chemistry principles. Herein, spindle-shaped MIL-53(Fe)-NH 2 @ZnIn 2 S 4 photocatalysts with a Z-scheme heterostructure were facilely developed for photocatalytic oxidation of aromatic alcohol in air under visible light. The benzyl alcohol conversion can be notably enhanced to 73% over the optimal MIL-53-NH 2 @ZnIn 2 S 4 sample with a benzaldehyde production rate of 1825 μmol g –1 h –1 . However, in the O 2 atmosphere, the benzyl alcohol conversion is only 56%, indicating that O 2 is not required and has an adverse effect on the reaction. The hierarchical structure and Z-scheme heterojunction of MIL-53-NH 2 @ZnIn 2 S 4 impart an efficient separation and strong redox abilities of photo-induced electrons and holes, which are responsible for the impressive photocatalytic performance. This study could motivate the ingenious design of Z-scheme heterostructures for green organic conversion based on MOFs.
✓ 已验证
产品关联
DOI
高影响因子
MICROCHIMICA ACTA
·
2022
·Vol. 189
·期 9
·1-13
·
IF 6.408
Chen Jing,Li Shuying,Chen Ying,Yang Jiao,Dong Jianbin
Adenine (A) and guanine (G) are mainly found in deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) and play a crucial role in genetic information transfer and protein synthesis. In this study, NH 2 -MIL-53(Fe)/CS/MXene nanocomposites were prepared for detecting guanine and adenine. With high specific surface area, excellent water dispersion, and numerous active sites, MXene (transition metal carbides, nitrides, and carbonitrides) provides a good platform for loading primitive metal-organic frameworks (MOFs). At the same time, the problem of poor conductivity and dispersion of MOFs is solved. The electrochemical catalytic oxidation of adenine and guanine of NH 2 -MIL-53 (Fe)/CS/MXene nanocomposites was carried out by differential pulse voltammetry (DPV). Operating voltage of DPV: 0.7–0.9 V (vs. Ag/AgCl) for G, 1.0–1.2 V (vs. Ag/AgCl) for A, 0.8 V (vs. Ag/AgCl), and 1.1 V (vs. Ag/AgCl) for G and A. The concentration ranges for detecting A and G were 3–118 μM and 2–120 μM with detection limits of 0.57 μM and 0.17 μM (S/N = 3), respectively. The nanocomposite was used for detecting G and A in herring sperm DNA, and the content of G and A was found to be about 9 and 11 μM; the RSD values were 3.4 and 1.3%, respectively. Graphical abstract
✓ 已验证
产品关联
DOI
PubMed
高影响因子
BIOCHEMICAL ENGINEERING JOURNAL
·
2022
·
IF 4.446
Xu Pan,Wenjing Wang,Ye Chen,Qing Wen,Xiaoqian Li,Cunguo Lin,Junhong Wang,Haitao Xu,Liuqingying Yang
As a promising green and storage/conversion technology, the microbial fuel cell (MFC) was generally restricted by the lower power density in application. Three carbonized derivatives of the same precursor metal organic framework (MOF) MIL-53(Fe) were prepared via carbonization at 385 ℃, 600 ℃ and 750 ℃ in argon atmosphere. Experiments showed that carbonized MIL-53(Fe) (CM53) derivative at 750 ℃ produced Fe 3 O 4 /Fe@C structure and revealed the best performance as bioanode in MFC. As anticipated, the MFC with CM53–750/Ti anode demonstrated superb maximum power density of 1179.08 mW/m 2 , which was 88.04% and 36.24% higher than that of MFC with CM53–385/Ti and CM53–600/Ti anode. Moreover, the charge transfer resistance of CM53–750/Ti (0.23 Ω) bioanode in MFC was 90.49% and 87.29% lower than that of CM53–385/Ti (2.42 Ω) and CM53–600/Ti (1.81 Ω) in MFC. The BCA method and high-throughput sequencing proved that CM53–750/Ti bioanode exhibited good biocompatibility and the function of screening the dominant bacteria for electricity generation. The results were mainly attributed to the synergistic effect of derived carbon, iron and Fe 3 O 4 nanoparticles (NPs). Fe 3 O 4 NPs and porous rod-like carbon promoted the enrichment and cultivation of microorganisms on the anode surface, while Fe NPs provided an efficient path for the transmission of extracellular electrons. This article proved that the carbonized derivatives of MOF have application potential in MFC.
✓ 已验证
产品关联
DOI
高影响因子
RARE METALS
·
2021
·Vol. 41
·期 4
·1265-1275
·
IF 4.003
Tian Kang-Hui,Duan Chan-Qin,Ma Qun,Li Xing-Long,Wang Zhi-Yuan,Sun Hong-Yu,Luo Shao-Hua,Wang Dan,Liu Yan-Guo
High entropy oxides (HEOs), as a new type of single-phase multielement solid solution materials, have shown many attractive features and promising application prospect in the energy storage field. Herein, six-element HEOs (CoNiZnFeMnLi) 3 O 4 and (CoNiZnCrMnLi) 3 O 4 with spinel structure are successfully prepared by conventional solid-phase method and present outstanding lithium storage performances due to the synergy effect of various electrochemically active elements and the entropy stabilization. By contrast, (CoNiZnFeMnLi) 3 O 4 delivers higher initial discharge specific capacity of 1104.3 mAh·g −1 , better cycle stability (84% capacity retention after 100 cycles at 100 mA·g −1 ) and rate performance (293 mAh·g −1 at 2000 mA·g −1 ) in the half-cell. Moreover, the full-cell assembled with (CoNiZnFeMnLi) 3 O 4 and LiCoO 2 provides a reversible specific capacity of 260.2 mAh·g −1 after 100 cycles at 500 mA·g −1 . Ex situ X-ray diffraction reveals the electrochemical reaction mechanism of HEOs (CoNiZnFeMnLi) 3 O 4 , and the amorphous phase and the large amount of oxygen vacancies were obtained after the initial discharge process, which are responsible for the excellent cycle and rate performance. This research puts forward fresh insights for the development of advanced energy storage materials for high-performance batteries. Graphical Abstract
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2021
·
IF 13.273
Chunfeng Shao,Lingmin Wu,Yinghua Wang,Konggang Qu,Hailiang Chu,Lixian Sun,Jianshan Ye,Baitao Li,Xiujun Wang
Single-atom catalysts (SACs) have sparked intense interest in heterogeneous catalysis lately, but insufficient accessibility of active sites restricts their further applications. Herein, a hydrangea-like carbon nanoparticle possessing highly open nanospaces and enhanced external surface area that fully exposes the catalytic sites is reported. By introducing mesoporous silica nanoparticles (MSNs), Fe-doping zeolitic imidazolate framework-8 (ZIF-8) precursors are assembled into a flower-like superstructure interlaced by porous nanosheets, which expand from inside out constructing an open and interconnected architecture. This unique structure can substantially liberate the densely dispersed but deeply buried Fe-N 4 sites inside carbon nanoparticles and accelerate mass transfer in the catalyst layer that increases active-site utilization. Furthermore, the physical and chemical properties of the assembled catalysts can be adjusted by the diameter (200, 300, and 500 nm) of MSNs. When the diameter was 500 nm, the optimal FeNC-F3 catalyst exhibited large specific surface area, maximum metal centers utilization, high oxygen reduction reaction efficiency, and excellent stability. The novel cathodic electrocatalyst achieved high power density of 0.32 mW cm −2 in microbial fuel cell and 288 mW cm −2 in Zn-air battery. This work established a realistic strategy for promoting the practical development of fuel cell catalysts.
✓ 已验证
产品关联
DOI
高影响因子
Journal of Cleaner Production
·
2021
·
IF 9.297
Weiye Wang,Qingliang Zhao,Jing Ding,Kun Wang,Junqiu Jiang
Bio-electro-Fenton powered by microbial fuel cell (MFC-powered BEF) can in-situ generate and utilize hydrogen peroxide to degrade refractory pollutants. Most of the previous works loaded transition metal on the cathode to participate in the Fenton reaction showed limited electrical or degradation performance. The coupling of alkaline-earth metal (Mg 0 and MgO) and transition metal on cathode could improve the electrochemical and catalytic properties of MFC-powered BEF system, which had not been reported so far. In this research, a novel cathode of Fe–Mn–Mg/carbon fiber (Fe–Mn–Mg/CF) was developed with good polymerization effect of Mg to Fe and Mn, and outstanding production of reactive oxide species (•OH and •O 2 − ), which further improved the overall electricity generation efficiency and enhanced the degradation of pollutants. Accordingly, the maximum power density generated in MFC-powered BEF system with Fe–Mn–Mg/CF cathode was 2.07 times higher than that of the frequently used Fe–Mn/CF. Owing to the superiority of surface holes and MgO in H + adsorption and electron transfer , the integration of Fe, Mn with Mg promoted the in-situ generation of H 2 O 2 and active radicals, resulting in the highest catalytic performance of degrading refractory pollutants . Initial pH, external resistance, initial concentration of contaminant and cycle use frequency of cathode were also evaluated on the degradation efficiency of the BEF system. Furthermore, reaction and degradation mechanisms were proposed from H 2 O 2 production and free radical characterization. Overall, this study provided a novel cathode preparation approach for the MFC-powered BEF system, which vastly promoted its electrochemical and catalytic properties.
✓ 已验证
产品关联
DOI
高影响因子
FUEL
·
2021
·
IF 6.609
Hanzi Liu,Yi Zhang,Haiming Wang,Changfu You
Selective non-catalytic reduction of NOx (SNCR) with NH 3 is commonly used in industrial facilities like circulating fluidized bed (CFB) furnaces. However, the strongly temperature-dependent de-NOx feature confines its applications in a specific temperature range (900–1050 °C). Here, we report a new strategy on using Fe-Ni-W exchanged zeolite (0.5FNW-H) as a catalyst to extend the SNCR temperature window. In the CFB reactor, a significant NOx conversion improvement ranging from 14.1% to 80.9% was achieved at 700 to 850 °C by applying the developed catalyst. Catalyst dosage of 4500 h −1 (GHSV), a particle diameter of 0.1–0.3 mm, and NH 3 injection position at the dense-phase zone were found preferred for NOx reduction with the highest efficiency of ~85% at 700 °C. The physicochemical properties of the catalysts remained stable after the circulating reactions in the CFB reactor. The developed catalyst is particularly applicable for improving the SNCR performance when the thermal power plants are operated at low loads.
✓ 已验证
产品关联
DOI
高影响因子
Journal of Cleaner Production
·
2021
·
IF 9.297
Lizhen Guo,Yuqi Wang,Meng Wang,Hiba Shaghaleh,Yousef Alhaj Hamoud,Xu Xu,He Liu
With the severe shortage of water resources and the low utilization efficiency of fertilizer, slow-release fertilizer equipped with water-absorbing and water-retaining capacity has captured much attention. Herein, by integrating metal-organic frameworks (MOFs) with cellulose nanofibres (CNFs) and sodium alginate (SA), a novel cellulose-based hydrogel (MIL-100(Fe)@CNF-SA) was fabricated that acted as a carrier for urea. The resultant hydrogel was not only qualified with a high surface area of 129.17 m 2 /g but also affluent in the hydrophilic groups . In parallel with the good water-holding capacity of 55% when the loading of the resultant hydrogel was only 0.5 g, the complete loss of the water in the treated soil was successfully slowed down by nearly 20 d compared with the soil without treatment. Urea (1.47 g/g) could be captured in the composite hydrogel , wherein the slow release of urea was achieved due to the synergism of the highly porous structure of the hydrogel and the crystals with a high specific surface area. Moreover, the positive effect of the resultant hydrogel on the growth of wheat was indexed to the germination rate, number of tillers, photosynthetic rate and chlorophyll content of the crop, which verified their further application in irrigating farming.
✓ 已验证
产品关联
DOI
高影响因子
BIORESOURCE TECHNOLOGY
·
2021
·
IF 9.642
Yifei Gao,Yihan Li,Lulu Chen,Jing Song,Ying Liu
Efficient ammonia and nitrite removal in low nutrient recirculating seawater of recirculating aquaculture system (RAS) is critical for healthy cultivation. However, it is hard for conventional biological aerated filters (BAFs) to meet this demand under short hydraulic retention time (HRT). The electrooxidation-BAFs (E-BAFs) were constructed for efficient seawater treatment in a RAS of Sebastes schlegelii , with high activity anodic catalyst Ni-Fe oxide-PEDOT. Satisfactory ammonia removal (88.2% in E-BAFs, 33.7% higher than the control, stage 3) and nitrite removal (69.9 % in E-BAFs, 45.3% in the control) were achieved at HRT of 50 min. The proportion of nitrifying bacteria ( Nitrospira, Nitrosomonas and Nitrosopumilus ) and nitrification/denitrification genes ( amo CAB, nxr AB, nar GHI, et. al ) were higher in E-BAFs than the control, suggesting better potential in functional bacteria enrichment. Aerobic colony number in RAS with E-BAFs was lower and specific growth rate (SGR) of Sebastes schlegelii (3.79%) was significantly higher, indicating a better culture effect.
✓ 已验证
DOI
PubMed
高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2022
·Vol. 57
·期 1
·526-537
·
IF 4.682
Xu Lin-Wei,Qian She-Liang,Dong Bao-Xia,Feng Li-Gang,Li Zong-Wei
Molecular complexes with active metal centers exhibit high activity and selectivity for electrochemical CO 2 reduction reaction (CO 2 RR), which represents a promising method for transforming greenhouse gas into valuable chemicals and feedstock. Using metal–organic frameworks (MOFs) to load the active molecular complexes then employing the combination with the carbonic conducting material may exhibit a beneficial effect for CO 2 RR. Herein, we obtained a composite catalyst named PCN-222(Fe)/CNTs, which was in situ synthesized through the solvothermal method that loads iron porphyrin-centered PCN-222(Fe) molecules onto CNTs. The catalyst PCN-222(Fe)/CNTs exhibits excellent electrocatalytic performance for CO 2 RR with a FE CO of 95.5% (m(Fe-TCPP):m(CNTs) = 1:30, written as PCN-222(Fe)/CNTs-30) and an overpotential ( η ) of 494 mV. In addition, the turnover frequency (TOF) is high as 448.76 h −1 (3.011 site −1 s −1 ) and the hydrogen evolution reaction (HER) is indistinctive. After long-term electrocatalysis of 10 h at −0.6 V vs. RHE, PCN-222(Fe)/CNTs-30 remained its high catalytic performance with average FE CO = 90%. This work provides a solid foundation for further research in the high-efficiency transformation of CO 2 to CO. Graphical abstract
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2021
·
IF 10.588
Pengyu Zhang,Xianfa Zhang,Xiaodan Zhao,Guohua Jing,Zuoming Zhou
Peracetic acid (PAA) is an excellent oxidant that can produce multiple carbon-centered radicals (R•C). A novel advanced oxidation process (AOP) that combines PAA and nanoscale zero-valent iron (i.e. nZVI/PAA) is constructed to evaluate its performance toward tetracycline (TC) abatement. The nZVI/PAA process shows excellent abatement efficacy for TC in the pH range of 3.5–7.5. The presence of humic acid , HPO 4 2− and HCO 3 − exerts inhibitory effects on TC abatement, while the presence of Cl − displays negligible influence in the nZVI/PAA process. Nanoscale zero-valent iron (nZVI) exhibits excellent reusability with no apparent variation in crystallinity . CH 3 C(O)OO• is the predominant active radical that contributes to TC abatement, in which leakage of Fe(II) from the nZVI surface is crucial for a radical generation. Due to the strong complexation tendency of TC towards Fe(II), the Fe(II)-TC complexes are formed, which significantly accelerates the PAA decomposition and TC abatement compared to free Fe(II). In addition, the degradation intermediates of TC are identified, and a possible degradation pathway is proposed. These results will be useful for the application of PAA-based AOPs in the treatment of water containing organic micropollutants.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）