Chemical Engineering and Processing-Process Intensification
·
2021
·
IF 4.237
Dicka Ar Rahim,Wei Fang,Gaojun Zhu,Haryo Wibowo,Dwi Hantoko,Qing Hu,Herri Susanto,Zengliang Gao,Mi Yan
Before syngas from gasification of biomass could be used as synthesis fuel or chemical feedstock, it requires the removal of hydrogen sulfide (H 2 S) to meet the purity standard level of those applications. In this study, Zn-Fe/Al 2 O 3 were successfully synthesized by a microwave-assisted wet incipient impregnation technique for use as adsorbent for H 2 S removal. The characterization of synthesized adsorbents showed that the oxide form of Zn and Fe present on the surface of adsorbents were zinc oxide (ZnO), magnetite (Fe 3 O 4 ), and zinc ferrite (ZnFe 2 O 4 ). While the reduction of adsorbent was mostly due to that of iron oxide . The reduced adsorbents might consist of ZnO/Fe 3 O 4 /FeO/Fe on alumina as support. At relatively high space velocity (26,000 h −1 ) the adsorbents were able to reduce the H 2 S concentration from 250 ppm at the inlet to around 45 ppm, 35 ppm, and 25 ppm at the outlet by adsorbent 1ZnFe, 2ZnFe, and 3ZnFe; respectively. The removal efficiency for adsorbent 1ZnFe, 2ZnFe, and 3ZnFe were 82%, 86%, and 90%; respectively. Results also shown an increase in adsorbent lifetime with the increase of the Zn to Fe ratio.
✓ 已验证
产品关联
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2017
·
IF 2.714
Xiaoqin Huang,Yanli Niu,Weihua Hu
Heterogeneous Fenton catalyst with high activity and excellent durability is highly demanded for efficient removal of organic pollutants via well-known Fenton reaction. In this work Fe/Fe 3 C nanoparticles loaded on iron/nitrogen-doped graphene (Fe/Fe 3 C @ Fe/N-Graphene) were synthesized via spontaneous oxidative polymerization of dopamine (DA) on graphene oxide (GO) surface in the presence of iron (III) chloride, followed by thermal annealing. The Fenton catalytic performance of as-prepared Fe/Fe 3 C @ Fe/N-Graphene was evaluated by degrading rhodamine 6G (Rh 6G) as a model organic pollutant. It is found that as-prepared catalyst demonstrates good activity with a rate constant of 0.080 min −1 under optimal hydrogen peroxide (H 2 O 2 ) concentration and catalyst dosage. Moreover, its catalytic activity shows negligible decrease even after 13 successive cycles, exhibiting excellent catalytic durability. The possible mechanism behind the improved Fenton catalytic activity and durability was further discussed.
✓ 已验证
产品关联
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2025
·
IF 6.9
Xiaolin Shi,Guo Yang,Bo Xing,Caiyi Jiang,Hangdao Qin,Min Li,Fuping Zhang,Yi Wang,Dongzheng Wang,Xingyong Liu
Fluorine-containing wastewater seriously threatens human health due to the wide application of sodium p -perfluorous nonenoxybenzenesulfonate (OBS). Herein, a novel Fe-Co bimetallic biochar (Fe-Co@BC) with abundant pore structure, functional groups and quickly electron transfer capability was prepared using hydrothermal method. Meanwhile, Fe-Co@BC-Ⅰ exhibited a superior catalytic capacity for degradation of OBS in PMS system, and the removal efficiency of OBS reached to 94.1 % within 60 min. After three cycles, the removal efficiency of OBS still up to 80 % and the Fe-Co had almost no leaching (Fe: 0.006 mg/L; Co: 0.023 mg/L). Further mechanistic insights were verified that high catalytic capacity and stability ascribed to the synergistic effects of Fe and Co, where Fe-Co mutual interaction promoted the formation of Fe 2+ and Co 2+ and accelerated electron transfer of catalyst. In addition, the quenching experiments and electron paramagnetic resonance (EPR) proved that the degradation of OBS can be mainly ascribed to indirect oxidation of SO 4 −• , O 2 −• and •OH, and the possible degradation pathway of OBS was proposed in the Fe-Co@BC/PMS system. This study provides an insight into bimetallic prepared and activation PMS degradation fluorinated wastewater.
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2024
·
IF 9.4
Yanyu Song,Xianbo Sun,Long D. Nghiem,Jun Duan,Wen Liu,Yongdi Liu,Zhengqing Cai
Building a heterojunction is a fascinating option to guarantee sufficient carrier separation and transfer efficiency, but the mechanism of charge migration at the heterojunction interface has not been thoroughly studied. Herein, MIL-53(Fe)/Bi 4 O 5 I 2 photocatalyst with a Z-scheme heterojunction structure is constructed, which achieves efficient photocatalytic decontamination under solar light. Driven by the newly-built internal electric field (IEF), the formation of Fe-O-Bi electron migration channel allows for rapid separation and transfer of charge carriers at the heterojunction interface, confirmed by the material characterization and density functional theory (DFT) calculation. The narrower band gap and improved visible light response also contribute to the enhanced photocatalytic activity of composite materials. With levofloxacin as the target pollutant, the optimal MIL-53(Fe)/Bi 4 O 5 I 2 achieves complete removal of pollutant within 150 min, the photocatalysis rate of which is ca. 4.4 and 26.0 times that of pure Bi 4 O 5 I 2 and MIL-53(Fe), respectively. Simultaneously, the optimal composite material exhibits satisfactory photodegradation of seven fluoroquinolones, and the photocatalysis rates are as follows: lomefloxacin > ciprofloxacin > enrofloxacin > norfloxacin > pefloxacin > levofloxacin > marbofloxacin. DFT calculations reveal a positive relationship between degradation rate and Fukui index (ƒ 0 ) of main carbon atoms in seven fluoroquinolones. This study sheds light on the existence of electron migration channels at Z-scheme heterojunction interface to ensure sufficient photoinduced carrier transfer, and reveals the influence of pollutant structure on photolysis rate.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2024
·
IF 11.2
Tao Zhao,Dazhong Zhong,Qiang Fang,Xin Zhao,Runxin Du,Genyan Hao,Guang Liu,Jinping Li,Qiang Zhao
The rational design of metal-organic frameworks (MOFs) provides potential opportunities for improving energy conversion efficiency. However, developing efficient MOF-based electrocatalysts remains highly challenging. Herein, a strategy involving strain engineering is developed to promote the electrocatalytic performance of MOFs by optimizing electronic configuration and improving the active site. As expected, the optimized CoFe–BDC NO 2 exhibits a low overpotential of 292 mV at 10 mA cm –2 and a small Tafel slope of 31.6 mV dec –1 as oxygen evolution reaction (OER) electrocatalyst. Notably, when CoFe–BDC NO 2 is prepared on Nickel foam (NF), the overpotential is only 345 mV at 1 A cm –2 , which ensures efficient water oxidation properties. Integrating CoFe–BDC NO 2 /NF anode in membrane electrode assembly (MEA) for overall water splitting and CO 2 reduction reaction (CO 2 RR) tests, the results show that the cell voltages of CoFe–BDC NO 2 /NF are 3.14 and 3.09 V at 300 mA cm –2 (25 °C), respectively, indicating that MOFs have various practical application prospects. The research of the structure-performance relationship reveals the lattice oxygen oxidation mechanism (LOM) where the Co-O-Fe bond is formed during the OER process by changing the electronic environment and coordination structure of CoFe–BDC NO 2 , and with high valence Co as active center, which provides a deep understanding of the structure design of MOFs and their structural transformation during OER.
✓ 已验证
产品关联
DOI
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2025
·
IF 21.1
Qingfei Zhao,Zhenpeng Guo,Zhuohan Wu,Shuyuan Dong,Ronghao Kang,Bingdian Jiang,Shuhui Guan,Ting Zhang,Zhenfeng Bian
The advanced oxidation process (AOP) based on hydroxyl radical ( • OH) has garnered increasing attention in water purification and wastewater treatment. However, producing • OH by activating hydrogen peroxide (H 2 O 2 ) encounters the challenges associated with the sluggish kinetics of Fe(II) regeneration. Herein, we developed a carambola-like catalyst of boron (B)-doped TiO 2 mesocrystals-based iron catalyst (Fe-B-MST), which served as a photocatalyst to modulate the regeneration of Fe(II) in photo Fenton-like systems. We successfully used the electrospinning method to gain membrane and realised the remediation of different industrial wastewater. The Fe-B-MST catalyst exhibits excellent efficiencies in the oxidative degradation of 4-chlorophenol (4-CP) pollutants, effectively facilitating the production of • OH while minimising the formation of toxic byproducts, with the first-order kinetic constant ( k = 2.372 min −1 ) being approximately 6.1 times greater than that without B doping, and 19.8 times greater than that observed with commercial TiO 2 . Theoretical calculations and related physicochemical characterisation reveal that B occupies an interstitial site in titania, conferring a sufficiently high valence band potential, making it thermodynamically favourable for H 2 O 2 oxidation and weakening its interaction with • OH, consequently increasing higher reactivity toward the targeted organic pollutant. The B doping facilitates electron transfer, promotes rapid reduction of Fe(III) to Fe(II), and further enhances • OH production via a photo Fenton-like reaction. The oxidation reaction stoichiometry efficiencies were quantified for different organics and calculated to be in the range of 7.70–24.20 % in Fe-B-MST/H 2 O 2 vis. system, representing an enhancement of 1.18–1.54 times compared to Fe-MST/H 2 O 2 vis. , alongside the utilisation efficiency of H 2 O 2 ( η ) of Fe-B-MST/H 2 O 2 vis. is 1.37–1.67 fold greater than that of Fe-MST/H 2 O 2 vis. after 30 min of reaction. This study expands our understanding and provides valuable insights into applying photocatalysis for enhanced wastewater treatment.
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL GEOLOGY
·
2024
·
IF 3.6
Kuan Cheng,Zesheng Yang,Guojun Chen,Shiwen Hu,Chao Guo,Yang Yang,Shan Wang,Ying Wang,Haibo Dong,Milan Wang,Pengfei Cheng,Tongxu Liu
The nitrate-reducing Fe(II)-oxidizing (NRFO) process plays a crucial role in geochemical Fe N coupled cycling under anoxic conditions. Both nitrate and nitrite can act as electron acceptors for NRFO bacteria, resulting in the formation of Fe(III) minerals. Nevertheless, the stability of Fe(III) minerals generated during the NRFO process remains unclear. In this study, the Fe(III) minerals were obtained using the model NRFO bacteria strain Acidovorax sp. BoFeN1 in the presence of nitrate or nitrite. The stability of the Fe(III) minerals was examined in the presence of the model Fe(III) reduction bacteria Shewanella oneidensis MR-1 (strain MR-1), the chemical reducing reagent sodium dithionite (Na 2 S 2 O 4 ), and hydrochloric acid (HCl), respectively. The main Fe(III) minerals were goethite in the nitrate treatments (named M nitrate ) and tightly attached to the surface of cells. Meanwhile, the main Fe(III) minerals were lepidocrocite in the nitrite treatments (named M nitrite ), showing slight adherence to the cell surface. The reductive dissolution kinetics of M nitrate by strain MR-1 revealed a gradual increase in Fe(II). Little Fe(II) was formed when reduced M nitrite , which was attributed to the residual nitrite acted as a competitive electron acceptor to Fe(III), inhibiting the microbial Fe(III) reduction processes. Furthermore, the Fe(III) minerals were harvested by centrifugation and then reacted with sodium dithionite and hydrochloric acid (HCl), respectively. The incorporation of sodium dithionite and hydrochloric acid facilitated the dissolution of Fe(III) minerals. In the M nitrite treatments, the Fe(III) minerals exhibit enhanced stability due to their inherent higher crystallinity and the protective influence of cell surface and microbial carbon. This study broadens our understanding of the formation and transformation of microbial Fe(III) minerals, thereby improving our knowledge of biogeochemical iron cycling under anoxic conditions.
✓ 已验证
产品关联
DOI
高影响因子
Environmental Science-Processes & Impacts
·
2025
·
IF 3.9
Rong Peng,Qi Zhu,Shuang Li,Hui Liu
The bacterium Comamonas terrigena strain HJ-2 has been reported as a nitrate-dependent iron-oxidizing bacterium, surprisingly with Fe(III) reduction ability. The control of iron redox cycling by the strain HJ-2 in the Fe(II)-Fe(III) co-existing system is mysterious and worthy of exploration. The present study demonstrates that HJ-2 utilizes nitrate as an electron acceptor to rapidly oxidize Fe(II), with negligible Fe(III) reduction, under neutral anaerobic conditions in a co-existing Fe2+ and ferrihydrite system. Nitrate significantly influences the iron transformation mediated by HJ-2. The final conversion ratio of Fe(II) increased from 27.94% to 96.67%, and the bio-oxidation rate of Fe(II) escalated from 0.000143 to 0.013 h⁻¹ as nitrate concentrations rose from 0.1 to 10 mM. X-ray diffraction results indicated that in the absence of HJ-2, goethite was the sole product, regardless of the nitrate concentration. While in the presence of HJ-2, the minerals formed transitioned from crystalline goethite and lepidocrocite to amorphous or weakly crystalline minerals with increasing nitrate concentration. Scanning electron microscopy and energy-dispersive X-ray spectroscopy showed that the morphology of the final mineral formed under high nitrate conditions resembled ferrihydrite, with higher carbon content on the mineral surface at elevated nitrate concentrations, suggesting enhanced production of bio-iron oxides and increased adsorption capacity for aqueous Fe(II). X-ray photoelectron spectroscopy results confirmed higher Fe(II) content on the amorphous minerals surface than goethite. This work provides new insights into microbial-mediated Fe-N cycling in natural environments, highlighting the significance of nitrate in driving iron redox processes and the iron mineral transformation by strain HJ-2.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Ting Zhou,Wenyi Dong,Xuechuan Li,Weigang Liu,Mengke Qiang,Hongjie Wang
High-valent ferric oxide species (HV-Fe(IV)) has been increasingly explored to selectively and efficiently remove pollutants from wastewater owing to its high reduction potential, long lifetime, and valuable resistance to anions. However, the directional production of HV-Fe(IV) and its mechanism remain challenging. Herein, a biochar-based catalyst with monoatomic Fe-trans-N 2 O 2 configuration and rich COOH group (SAFe-NKBC) was rationally constructed via KOH and supramolecular organic framework co-pyrolysis. As a result, the SAFe-NKBC/PMS system exhibited exceptional catalytic performance, achieving rapid sulfamethoxazole degradation (97.4% within 10 min) and TOC removal (73.1%). Mechanistic investigations revealed the cooperative catalytic role of single-atom Fe-trans-N 2 O 2 and COOH in biochar support via surface-confinement effect in boosting peroxymonosulfate activation and directional HV-Fe(IV) generation, mediating spatially coupled electron transfer and promoting selective oxidation pathways. Furthermore, a structure–activity relationship for various para-substituted anilines was systematically established via quantitative structure–activity relationship modeling based on different adsorption and oxidation descriptors. The valid descriptors were confirmed to predict reactivity, offering a molecular-level framework for water purification. Meanwhile, the catalyst demonstrated excellent resistance to matrix interference, long-term stability in flow-through systems, and significantly reduced toxicity of degradation byproducts, underscoring its potential in sustainable and precision-oriented water remediation. This work offered new insights into rational SAC design and reactivity prediction for sustainable water remediation.
✓ 已验证
产品关联
DOI
高影响因子
Sustainable Energy & Fuels
·
2020
·Vol. 4
·期 5
·2192-2200
·
IF 5.503
Zhewen Ma,Qiuyu Zhang,Wen Zhu,Darvaish Khan,Chuanzhu Hu,Tianping Huang,Wenjiang Ding,Jianxin Zou
TMA-TM (TM = Fe, Ni) MOFs were synthesized successfully by a facile method. A MgH2-TM MOF (TM = Fe, Ni) composite was obtained via ball milling and the corresponding hydrogen storage performance was investigated. Particularly, high-resolution transmission electron microscopy was performed to in situ characterize the dehydrogenation behavior of the MgH2-TM MOF composite. The results reveal that nano α-Fe and Mg2NiH4/Mg2Ni derived from the TMA-TM MOFs display a synergetic improving effect on the de/hydrogenation of MgH2. During the hydrogen desorption process, Mg2NiH4/Mg2Ni works as a “hydrogen pump” to quickly deliver hydrogen and facilitates hydrogen diffusion. Meanwhile, α-Fe accelerates the nucleation and growth of Mg by reducing the nucleation energy of Mg from MgH2. The hydriding activation energy of the MgH2-TM MOF declines to 45.3 kJ mol−1 H2. Meanwhile, the peak dehydriding temperature of the MgH2-TM MOF is 530.9 K, which is much lower compared with the MgH2–Fe MOF composite (541.7 K) and as-milled MgH2 (685.2 K). Therefore, nano Mg2Ni and α-Fe derived from the TMA-TM MOFs can remarkably improve the hydrogen storage properties of the MgH2/Mg system due to their synergetic catalytic effects.
✓ 已验证
DOI
高影响因子
Journal of Environmental Sciences
·
2024
·
IF 5.9
Zheng Qi,Zaihui Huang,Chunguang Liu
Advanced oxidation processes (AOPs) exhibit significant potential for water disinfection due to their generation of large quantities of highly oxidizing free radicals. However, the neglect of viable but nonculturable (VBNC) cells obscures their true disinfection efficacy and potential environmental health risks. Therefore, the study evaluated the disinfection effectiveness and mechanisms of typical AOPs, including Fe/H 2 O 2 , Fe/persulfate (PS), and O 3 , from the perspective of the production of VBNC bacteria. The results indicate that Fe/PS exhibits the strongest bacterial inactivation rate (99.94%), and the cells lose their ability to reactivate. Fe/H 2 O 2 and O 3 induce more cells to enter the VBNC state compared to Fe/PS. Moreover, different AOPs result in varying levels of free radical production and utilization efficiency, with SO 4 •− and O 3 exhibiting greater selectivity in deactivating bacteria compared to HO • . The inhibition of VBNC bacteria production by Fe/PS treatment may be attributed to the combined action of HO • and SO 4 •− on microorganisms, leading to oxidative stress and metabolic disruption in bacteria through the inhibition of biofilm formation and aminoacyl-tRNA biosynthesis ( p < 0.05), thereby causing direct bacterial death rather than entry into the VBNC state. In contrast, Fe/H 2 O 2 and O 3 result in the upregulation of the metabolism of alanine, aspartate, and glutamate, as well as styrene degradation capacity by the bacteria, leading to the production of more VBNC bacteria. Overall, the study offers insights into mitigating potential biological risks in water disinfection and developing environmentally friendly and efficient disinfection technologies.
✓ 已验证
DOI
PubMed
高影响因子
Scientific Reports
·
2015
·Vol. 5
·期 1
·1-13
·
IF 5.578
Ye Yi Quan,Jin Chong Wei,Fan Shi Kai,Mao Qian Qian,Sun Cheng Liang,Yu Yan,Lin Xian Yong
Cell wall is the major component of root apoplast which is the main reservoir for iron in roots, while nitric oxide (NO) is involved in regulating the synthesis of cell wall. However, whether such regulation could influence the reutilization of iron stored in root apoplast remains unclear. In this study, we observed that iron deficiency elevated NO level in tomato ( Solanum lycopersicum ) roots. However, application of S-nitrosoglutathione, a NO donor, significantly enhanced iron retention in root apoplast of iron-deficient plants, accompanied with a decrease of iron level in xylem sap. Consequently, S-nitrosoglutathione treatment increased iron concentration in roots, but decreased it in shoots. The opposite was true for the NO scavenging treatment with 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide (cPTIO). Interestingly, S-nitrosoglutathione treatment increased pectin methylesterase activity and decreased degree of pectin methylation in root cell wall of both iron-deficient and iron-sufficient plants, which led to an increased iron retention in pectin fraction, thus increasing the binding capacity of iron to the extracted cell wall. Altogether, these results suggested that iron-deficiency-induced elevation of NO increases iron immobilization in root apoplast by decreasing pectin methylation in cell wall.
✓ 已验证
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）