SEPARATION AND PURIFICATION TECHNOLOGY
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2023
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IF 8.6
Jingyu Ren,Xinyi Yang,Zhouzhou Yao,Qian Wei,He Guo,Zhirui Niu,Jian Wang,Jin Han,Jijiang Wang,Yanzhong Zhen
In this study, dielectric barrier discharge (DBD) plasma and F/FeO catalyst were utilized to degrade chloramphenicol (CAP) in water. The operation conditions, catalyst properties and catalytic mechanisms were systematically studied, and the anti-bonding activation effect was highlighted as the key for the catalytic effect. The results show that CAP was 100% degraded by DBD and F/FeO after 8 min treatment under optimal operating conditions, and F/FeO catalyst increased the degradation efficiency of CAP by 34.1%. FeO transferred electrons into the π* anti-bonding orbital of O 3 and the σ* anti-bonding orbitals of H 2 O 2 and O 2 , leading to an anti-bonding activation effect and weakening their bonding. Additionally, F facilitated the electron transfer of FeO and changed the stable adsorption of O 3 and H 2 O 2 on FeO to dissociated adsorption on F/FeO. The –OH groups generated by the H 2 O 2 dissociation could induce a non-Fenton catalytic pathway. The intensive electron transfer of F/FeO converted O 2 into ·O 2 − . The ant-bonding activation of O 3 , H 2 O 2 and O 2 on F/FeO facilitated the production of ·OH. A degradation pathway for CAP was proposed based on the findings of experiments and simulation. The developmental toxicity of CAP was weakened after F/FeO/DBD treatment. This study proposes an efficient plasma catalyst for purifying antibiotic wastewater, and provides a new insight into the mechanism of the plasma/catalysis process.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2022
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IF 5.518
Zewei Liang,Jing Wen,Yuanliang Zhou,Tingting Liu,Jinmei Dong,Weixin Zheng,Chenggong Chang,Xueying Xiao,Qiyuan Liu,Xiaogang Zheng
BiOCl 0.5 X 0.5 (X = F, Br, and I) heterojunctions were prepared via the solvothermal approach to achieve the solar-light induced photodegradation of tetracycline hydrochloride (TCH). The photocatalytic activity of BiOCl coupling with BiOI is greatly affected by the molar ratio of Cl/I. The best photocatalytic efficiency of 97.9 % within 120 min is obtained by flower-like BiOCl 0.5 I 0.5 microspheres with a Cl/I molar ratio of 1:1, and the removal efficiency of TCH over BiOCl 0.5 I 0.5 declines to 93.2 % after five cycles. Compared with BiOCl 0.5 Br 0.5 and BiOCl 0.5 F 0.5 , BiOCl 0.5 I 0.5 presents the better photocatalytic activity . Z-scheme junction between BiOCl and BiOI is favorable for the efficient separation and migration of photo-generated charge carriers, and the narrow band-gap structure of BiOCl 0.5 I 0.5 microspheres favors the visible-light harvesting.·O 2 - plays a vital role in BiOCl 0.5 I 0.5 -assisted photocatalytic reaction. However, the change in valance states induced by photo-corrosion is responsible for the solar-light deactivation of BiOCl 0.5 I 0.5 .
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Inorganic Chemistry Frontiers
·
2022
·Vol. 9
·期 18
·4705-4713
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IF 7.779
Ting Zheng,Qiang Wang,JinXuan Ren,Liling Cao,Ling Huang,Daojiang Gao,Jian Bi,Guohong Zou
Generally, phosphates are employed to design ultraviolet nonlinear optical crystals. However, phosphates always suffer from too small birefringence to effectively achieve phase matching. Herein, the Sn2+ cation with a stereochemically active lone pair was introduced into a phosphate as a birefringence-active unit, and two tin phosphate halides Sn2PO4X (X = F, Cl) were successfully synthesized. Interestingly, the different coordination environments of the Sn-polyhedron caused by the partial substitution of halide ions (F−/Cl−) with different ionic radii for the oxygen ligands lead to structural transformation from centrosymmetric (CS) Sn2PO4F to noncentrosymmetric (NCS) Sn2PO4Cl. Thus, Sn2PO4X (X = F, Cl) were characterized by enlarged birefringence, and Sn2PO4Cl is type I phase-matchable with a moderate SHG response, and is a potential ultraviolet nonlinear optical material. Furthermore, both phosphates show wide band gaps. Theoretical analysis confirmed that their excellent optical properties result from the synergistic effect of the [SnOX] (X = F, Cl) polyhedra with stereochemically active lone pairs and the [PO4]3− tetrahedron.
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ENVIRONMENTAL POLLUTION
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2022
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IF 9.988
Jingqi Ruan,Tianhao Tang,Ming Zhang,Weichuan Qiao
The coexistence of per- and polyfluoroalkyl substances (PFASs) and heavy metals have been found in soils. However, the interaction between the combined pollutants in soils remains unclear. In this study, the adsorption processes of single and combined Cr(VI) and chlorinated polyfluoroalkyl ether potassium sulfonate (F–53 B) in red, yellow and black soils were simulated. When compared with the single F–53 B and Cr(VI), the adsorption amount of the combined F–53 B and Cr(VI) on soils changed with the types of soils. The interactions between F–53 B and Cr(VI) in soils affected their adsorption behavior. The adsorption of the combined F–53 B and Cr(VI) best fit second-order kinetics and the Freundlich equation. Moreover, aluminum and iron oxides are highly correlated with adsorption of F–53 B and Cr(VI). Both F–53 B and Cr(VI) can form complexes with aluminum and iron oxides through electrostatic interactions, but PFOS could be bridged with iron oxides to form an inner sphere complex and with aluminum oxides to form an outer sphere complex. The coexistence of F–53 B and Cr(VI) could change the fluorescent group of dissolved organic matter (DOM) in soils due to the complexation between F–53 B and DOM. In addition, F–53 B increased the acid-soluble portion of Cr and decreased its residual form, which promoted the environmental risk of Cr in soils.
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Inorganic Chemistry Frontiers
·
2022
·Vol. 9
·期 10
·2298-2304
·
IF 7.779
Jiongquan Chen,Wenqi Jin,Yanhui Zhang,Yun Yang,Zhihua Yang,Shilie Pan
A new alkaline-earth and rare-earth borate fluoride, Ba10LuB18O32F13, the first example of borate in the Lu–B–O–F system, has been successfully synthesized in a high-temperature vacuum system. It crystallizes in the orthorhombic system, with the Fmm2 space group and the parameters a = 16.5749(6) Å, b = 16.7644(9) Å, c = 13.6222(6) Å, and Z = 4. It represents a new fundamental building block (FBB), [B9O22], with the notation 9:[2(4:2Δ + 2T) + T], in which two [BO3] triangles and two [BO4] tetrahedra are enclosed into a [B4O10] ring and every two [B4O10] rings are bridged by a [BO4] tetrahedron. The [B9O22] FBBs are further condensed into a 3D network with two types of channels that accommodate Ba2+ and Lu2+ cations. The UV cut-off edge is below 190 nm, indicating the application potential of Ba10LuB18O32F13 in the DUV region. Additionally, to further explore the structural novelty of Ba10LuB18O32F13, a comparison with all anhydrous borates with 18 boron atoms in their chemical formula was carried out. The fascinating results indicate that [B9O22] has been discovered for the first time, enriching borate fluoride structure chemistry.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2022
·
IF 9.965
Dexin Xu,Jing Yao,Xinzhi Ma,Yan Xiao,Chi Zhang,Wei Lin,Hong Gao
Electrochemical water splitting, the most direct and clean method used for the production of hydrogen, requires highly efficient bifunctional electrocatalysts that can accelerate hydrogen evolution reactions (HER) and oxygen evolution reactions (OER) by overcoming their kinetics barriers. Herein, self-supported F, N codoping CoP nanosheets (denoted as FN-CoP NS) are prepared as efficient and stable bifunctional electrocatalysts. Codoping of F and N neutralizes the electronegativity of surface P-O by cleaving the Co-P-O of non-metallic P sites on the surface (O derived from the surface oxidation). This contributes to an increased Co 2+ content with considerable adjustable electronegativity and also optimizes HER and OER processes. As a result, FN-CoP NS requires 66 and 241 mV overpotentials to deliver the current density of 10 mA cm −2 during HER and OER, respectively. A full water electrolyzer equipped FN-CoP NS as both cathode and anode only require 1.57 V to drive the current density of 10 mA cm −2 and to sustain 50 mA cm −2 for 48 h. This work adjusts the electronic structure of metal phosphides by a double anion codoping strategy, which provides a reference value for the rational design of efficient bifunctional electrocatalysts.
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SENSORS AND ACTUATORS B-CHEMICAL
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2022
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IF 9.221
Rouying Cai,Chenfang Miao,Liang Zhang,Yi Zhou,Yuebin Liu,Chen Zheng,Wendi Han,Zhengjun Huang,Xin Zhou,Shaohuang Weng
Tigecycline (TIGE) plays a significant role in the management of complex and serious bacterial infection. The monitoring of TIGE content in plasma and the further application in pharmacokinetic (PK) study is important for clinical medicine, however, the facile and effective strategy is limited. Herein, a sensitive, accurate and facile method for TIGE detection was developed by fluorescence with F, N codoping carbon dots (F, N-CDs) as probe. F, N-CDs exhibited stable maximum emission fluorescence at 500 nm and large Stokes shift of 135 nm. Such property help to weaken the possible self-absorption of biological system and the spectral overlap of fluorophore . Thus, using F, N-CDs as probe, the method exhibited accuracy and similarity of the analytical performance of TIGE detection in human plasma and rat plasma. The validated method was successfully applied to the PK research of TIGE in rat after intravenous injection at three dose levels of 1 μg/g, 2 μg/g, and 4 μg/g at different time-points. The obtained PK parameters of TIGE using this method were basically consistent with current clinical practice. The findings demonstrated the application ability of F, N-CDs for PK study of TIGE ascribed to the clinical need of simple operation, accuracy and rapidity.
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PLoS One
·
2021
·Vol. 16
·期 12
·e0260747
·
IF 3.24
Yang Yang,Yipeng Chen,Jimiao Cai,Xianbao Liu,Guixiu Huang
The soil-born filamentous fungal pathogen Fusarium oxysporum f. sp. cubense (FOC), which causes vascular wilt disease in banana plants, is one of the most economically important Fusarium species. Biocontrol using endophytic microorganisms is among the most effective methods for controlling banana Fusarium wilt. In this study, volatile organic compounds (VOCs) showed strong antifungal activity against FOC. Seventeen compounds were identified from the VOCs produced by endophytic fungi Sarocladium brachiariae HND5, and three (2-methoxy-4-vinylphenol, 3,4-dimethoxystyrol and caryophyllene) showed antifungal activity against FOC with 50% effective concentrations of 36, 60 and 2900 μL/L headspace, respectively. Transmission electron microscopy (TEM) and double fluorescence staining revealed that 2-methoxy-4-vinylphenol and 3,4-dimethoxystyrol damaged the plasma membranes, resulting in cell death. 3,4-dimethoxystyrol also could induce expression of chitin synthases genes and altered the cell walls of FOC hyphae. Dichloro-dihydro-fluorescein diacetate staining indicated the caryophyllene induced accumulation of reactive oxygen species (ROS) in FOC hyphae. FOC secondary metabolism also responded to active VOC challenge by producing less fusaric acid and expressions of genes related to fusaric acid production were interrupted at sublethal concentrations. These findings indicate the potential of S . brachiariae HND5 as a biocontrol agent against FOC and the antifungal VOCs as fumigants.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2021
·
IF 7.312
Tongtong Ren,Suli Liu,Hong Li,Angui Zhang,Xingang Li,Wei Yuan,Xin Gao
Utilization of F-T synthetic to produce value-added C 8 linear α-olefin is a promising alternative approach, however, the purification of α-olefin from F-T synthetic products is a great challenge, especially for removing 2-methyl-1-heptene (MH). This article addresses the novel method of etherification reaction to remove MH from F-T synthetic products, and develop by far the most efficiency reactive distillation (RD) method to intensified the etherification process. The scarcity of thermodynamic data was measured and regressed by the activity coefficient models, furthermore, kinetics of the etherification reaction of MH with methanol was explored using an ion exchange resin as catalyst, and then fitted by a pseudo-homogeneous model. The pilot-scale RD experimental results show that the conversion of MH reaches 91.83 % and the purity of α-olefin increases by 14.9 wt% (percentage points). Process analysis method was used to realize the optimization of design and operating parameters of etherification RD column based on the developed rigorous model. The optimization results show that the conversion of MH achieves 99.74 % and the purity of α-olefin achieves 96.87 wt%, which is also illustrated that the novel method for removing MH is proposed paving the way for purification of α-olefin from F-T synthetic products.
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JOURNAL OF ORGANIC CHEMISTRY
·
2023
·
IF 3.6
Qijie Zou,Wei Zhang,Haoyue Wang,Guangwei Yin,Yongzhi He,Fangyi Li
The CF3 group attached to N-aryl hydrazone could be activated upon treatment with a suitable base, thus serving as an excellent C1 unit for the assembly of a series of 1,3,4-oxadiazoles by reaction with hydrazides. The transformation is proposed to proceed via the intermediate formation of a gem-difluorinated azoalkene. Furthermore, this reaction features simple conditions and a broad substrate scope with respect to both trifluoromethyl N-aryl hydrazones and hydrazides.
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JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY
·
2020
·
IF 1.701
Huili Zhang,Hailin Yu,Wen Yuan,Bo Yu,Ying Chen,Jinjun Deng,Danfeng He,Ye Zhang
Co2+ and F– are doped into lattice of TiO2 powders, and the effects on charge trapping, recombination, and interface transfer are systematically researched. Double doped TiO2 photocatalyst was introduced on Graphene oxide, to construct heterojunction for photocatalytic denitrification of fuel containing pyridine (PY), indole (IND), and quinoline (QUI). A significant improvement in the photocatalytic activity was detected with the double doped modified heterojunction photocatalyst as compared to the pure TiO2. The reason for the improvement of the photocatalytic denitrification performance of oil may be derived from that the doped metal ions and nonmetal ions capture charge carriers to provide an alternative pathway for interface charge transfer, decreased the band gap width and the energy required for the transition, and caused the red shift in the light response range. On the other hand, catalyst supported on RGO, not only accelerated the transfer of photogenic carriers, improved the life of catalytic active component, but also enhanced the dispersibility of catalyst in oil. The experimental results showed that the activity and reusability of the photocatalyst denitrification performance was found satisfactory. On this basis, it is indicated that Co2+/F–/TiO2-RGO can be prospective materials for catalytic denitrification of oil.
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ENVIRONMENTAL POLLUTION
·
2020
·
IF 6.793
Zhiming Xiao,Ruiguo Wang,Decheng Suo,Shi Wang,Xiaomin Li,Shujun Dong,Tong Li,Xiaoou Su
Increasing concerns over bisphenol A (BPA) as an endocrine disrupting chemical (EDC) and its adverse effects on both humans and animals have led to the substitution by structural analogs, such as bisphenol F (BPF), in many application areas. Information regarding to the carry-over of this emerging chemical in farm animals is essential for legislation and risk assessment purposes. In this study, a large-scale number of animal experiments were designed to investigate the transfer of BPF from feed to eggs. One control and three experimental groups of laying hens (72 hens per group) were fed with basal diets and BPF-contaminated feed at concentration levels of 0.1, 0.5 and 2.5 mg kg −1 , respectively, for two weeks. The hens were then fed with BPF-free diets for a further four weeks. Eggs were collected daily, and separated into egg yolk and white for BPF analysis. The effects of different levels of BPF exposure on laying performance followed a non-monotonic dose-response curve, since low level BPF (0.1 mg kg −1 ) exposure did increase the laying rate, mean egg weight and daily feed intake, while high level BPF (2.5 mg kg −1 ) exposure showed a decreasing trend. BPF residues were detected in both egg yolks and whole eggs after two days of administration, and plateau phase was achieved within 9–18 days. There are clear linear dose-response relationships between the plateau BPF concentrations in feed and eggs. The residue of BPF was found mainly in egg yolks with conjugated form and depleted slowly (still detected 21 days after feeding the BPF-free diet of the high level group). Mean carry-over rate of 0.59% BPF from feed to eggs was obtained. Compared with the carry-over rates of PCBs and dioxins, BPF showed a relatively minor trend of bioaccumulation in eggs. To the best of our knowledge, this is the first report on the deposition, depletion, and bioaccumulation study of bisphenols in farm animals. The quantity of data can therefore be helpful in the frame of risk assessment, especially for a comprehensive estimation of consumer exposure to the residues of bisphenols.
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