OPTICAL MATERIALS
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2023
·
IF 3.9
Han Kang,Ze Zhang,Wei Zhou
Rhodamine B(RhB) was encapsulated in Tb(btc) (btc = 1,2,4-benzene tricarboxylic acid) frameworks by “one-pot” method, and the complex RhB@Tb(btc) with host-guest dual fluorescence emissions was synthesized. Compared with the stability of Tb 3+ emission, the characteristic emission of RhB at 620 nm showed a more sensitive response to ambient temperature. By integrating the different temperature dependence of Tb 3+ and RhB emissions, the temperature sensing of RhB@Tb(btc) was determined with relative sensitivity ranging from 0.43 to 0.59% K −1 (temperature range 298–353 K). Among several common antibiotics, RhB@Tb(btc) showed fluorescence quenching response to metronidazole (MDZ) and color transition to levofloxacin (LOFX) respectively with stable reusability. The combination of photoinduced electron transfer and internal filtration effect was confirmed as the contributor to MDZ induced fluorescence quenching. Furthermore, hydrogels and milk, which were added antibiotics on purpose for simulating unsafe foods, were detected at in situ temperature by RhB@Tb(btc) test paper, which achieved highly sensitive and highly selective detection to MDZ and LOFX with limit of detection reaching 10 −6 M.
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2023
·
IF 5.8
Zhong Dengjie,Liu Peng,Liu Yi,Xu Yunlan
The Zn/Fe@N-doped porous graphitic carbon catalyst (Zn/Fe@PCN) was successfully produced through one-step pyrolysis of g-C 3 N 4 and Zn/Fe-MOF and was used for the activation of persulfate (PS) for the degradation of RhB. The Zn/Fe@PCN/PS system was able to degrade 95.92% of RhB in 30 min at a rate of 0.6453 min −1 when RhB was concentrated at 50 mg L −1 . The efficient degradation of RhB is primarily realized through the synergistic activation of PS by Zn, Fe, and N to produce reactive oxygen species 1 O 2 , \(\cdot{\mathrm{O}}_2^-\) , \(\cdot \mathrm{SO}_4^-\) , and ·OH. Zn 0 /Fe 0 in Zn/Fe@PCN forms a galvanic cell with carbon to release electrons to join in the activation of PS. The doping of Zn not only provides sufficient electrons for the activation of PS but also promotes the effective reduction of Fe 2+ and thus the Fe 2+ /Fe 3+ cycle. The N doping accelerates the electron transfer during the reaction progress.
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2023
·
IF 4.5
Jinfei Hu,Hang Zhu,Min Lin,Duoer Wu,Jianguo Yao,Tianyu Sun,Xiangjuan Ma,Yijing Xia
The objective of this research is to develop an effective electrocatalytic filtration system using Ti/SnO 2 -Sb membrane anodes for eliminating Rhodamine B (RhB) from wasteater. Compared to Ti/SnO 2 -Sb plate anode, the prepared Ti/SnO 2 -Sb membrane anodes featured smaller particle size, bigger electrocatalytic active surface area, lower charge transfer resistance, and higher potential for oxygen evolution. The electrocatalytic filtration system obtained RhB removal of 90.29% with EE/O of 5.51 kWh m −3 after 90 min of electrolysis when initial pH value was 5, current density was 10 mA cm −2 , initial RhB concentration was 50 mg L −1 , and membrane flux was 2.17 m 3 (m 2 ·h) −1 , respectively. The flow-through electrocatalytic filtration system was found to be limited by kinetics under a high membrane flux and dominated by an indirect radical oxidation. Finally, the possible RhB degradation pathways were proposed based on the detected intermediates and density functional theory calculations.
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Journal of Water Process Engineering
·
2023
·
IF 7
Fuwang Zhao,Yanling Yang,Siyang Ji,Rui Yu,Xing Li,Zhiwei Zhou
A photo-Fenton catalyst Fe‑carbon nitride (g-C3N4)/reduced graphene oxide (rGO) (labeled as FNGO) was prepared via two-step calcination thermal polymerization. rGO as a carrier of Fe-g-C3N4 accelerated the charge transfer and improved the reduction of Fe (III) as compared those of the binary Fe-g-C3N4 catalyst. The FNGO catalyst maintained a high surface area of 264.7 m2/g and its charge transfer rate was 2.77 times higher than Fe-g-C3N4. The decreasing transient photocurrent and increasing electrode resistance of FNGO, Fe-g-C3N4 and g-C3N4 confirm the positive synergistic effect of Fe N coordination and rGO in charge transfer. Under the synergistic of visible light irradiation and H2O2, the excellent degradation performance of FNGO towards rhodamine B was achieved (95.3 % removal) at Fe-doping content of 10 wt%, rGO loading content of 0.5 % and H2O2 addition of 1.5 mM. Hydroxyl radicals played a dominant role in the photocatalysis-Fenton system, which was related to the coordination of Fe N, the carrier off-domain of rGO, and the Fe (III)/Fe (II) cycle promoted by photogenerated electron and superoxide radicals. The FNGO had a high stability, a wide pH adaptation (3– 11) and a low Fe-leaching. This novel ternary light-driven photo-Fenton catalyst of FNGO enabled efficient decontamination during advanced treatment of wastewater.
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APPLIED CATALYSIS A-GENERAL
·
2022
·
IF 5.723
Wen Lu,Chen Wang,Yanan Han,Yuxuan Bai,Siyi Wang,Wenke Xi,Jianjun Wang
Covalent organic frameworks (COFs) have been widely used based on their ordered pore structure, inherent porosity, high specific surface area and excellent stability. Herein, the active two-dimensional COF (named HDU-25) photocatalyst was preformed by the solvothermal method, and the structure and morphology were characterized and analyzed. The effects of key factors on rhodamine B (RhB) degradation by HDU-25 were evaluated. The results showed that under suitable conditions, HDU-25 exhibited an excellent photocatalytic degradation rate of 99.9% for persulfate-assisted photocatalytic degradation of RhB, and HDU-25 also had superior stability and reusability. In addition, the mechanism of RhB degradation was investigated using free radical capture experiments and electron spin resonance (ESR) experimental analysis. The intermediates were detected by high performance liquid chromatography-mass spectrometry (HPLC-MS), and possible degradation pathways were suggested. The results of this research highlight the potential of HDU-25 photocatalysts to degrade organic dyes in wastewater.
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CHEMOSPHERE
·
2022
·
IF 8.943
Dongdong Liu,Dengqian Chen,Zhengkai Hao,Yibo Tang,Lipeng Jiang,Tianqi Li,Bing Tian,Cuiping Yan,Yuan Luo,Boyin Jia
In this work, a comparative study of efficient degradation of Rhodamine B (RhB) in CoFe 2 O 4 /H 2 O 2 and CoFe 2 O 4 /PMS systems was performed. Batch experiments indicated that the RhB degradation rate of CoFe 2 O 4 /H 2 O 2 system reached 95.5% at 90 min under the condition of 0.5 g L −1 of CoFe 2 O 4 dosage, 10 mM of H 2 O 2 concentration and 3.0 of initial pH. At certain conditions of initial pH = 7.0, 0.3 g L −1 of CoFe 2 O 4 dosage, 7 mM of PMS concentration, CoFe 2 O 4 /PMS system could completely degrade RhB within 90 min. EPR and quenching experiments indicated that •OH was the main active species of CoFe 2 O 4 /H 2 O 2 system, and •OH, SO 4 • - , •O 2 − and 1 O 2 participated in RhB degradation of CoFe 2 O 4 /PMS system. The circulate of Co(II)/Co(III) and Fe(II)/Fe(III) on the CoFe 2 O 4 surface promoted the formation of free radical species in the two system. In CoFe 2 O 4 /PMS system, the formed •O 2 − and SO 5 • - realized the generation of non-free radical species ( 1 O 2 ). The LC-MS results indicated that N -de-ethylation, chromophore cleavage, opening rings and mineralization were the main steps for the RhB degradation of the two systems. After five cycles of degradation experiment, the CoFe 2 O 4 /H 2 O 2 and CoFe 2 O 4 /PMS systems still maintained the high degradation rate (85.2% and 92.4%) and low mass loss (2.7% and 3.09%). In addition, CoFe 2 O 4 /PMS system had better potential value for the actual water and multi-pollutant degradation than CoFe 2 O 4 /H 2 O 2 system. Finally, the toxicity analysis and cost assessment of the two oxidation systems were preliminarily evaluated.
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JOURNAL OF THE CHINESE CHEMICAL SOCIETY
·
2023
·Vol. 70
·期 7
·1481-1492
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IF 1.8
Jia-Rong Xue,Rong-Chao Xue,Pei-Yao Chen,Yong Wang,Li-Ping Yu
In this study, a hydrostable Z-scheme Ag/CsPbBr 3 /Bi 2 WO 6 photocatalyst was designed and fabricated for the degradation of Rhodamine B (RhB). The structural instability of CsPbX 3 perovskites in water is one of the main obstacles that restrict their practical application in photocatalytic wastewater treatment. The photocatalyst was prepared in three steps: passivation of CsPbBr 3 nanocrystals (NCs) with 3-mercaptopropionic acid (MPA), construction of a heterojunction between MPA-passivated CsPbBr 3 NCs and Bi 2 WO 6 ultrathin nanosheets, and doping Ag nanoparticles as charge mediators in the heterojunction. The as-obtained 5%Ag/20%CsPbBr 3 /Bi 2 WO 6 exhibits good stability and excellent photocatalytic activity. The degradation rate is 93.9% in 120 min, which is 4.41 times than that of Bi 2 WO 6 .
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Reaction Kinetics Mechanisms and Catalysis
·
2021
·Vol. 134
·期 2
·1003-1015
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IF 2.081
Chen Anna,Zhang Jin,Zhou Yi,Tang Haiqin
In this study, the MOF-5/BiOBr photocatalyst with microsphere structure was synthesized by hydrothermal method for the first time. The crystal structure, morphology, photoelectric performance and photocatalytic activity of the samples were characterized by XRD, SEM, TEM, XPS and electrochemistry. The results show that the synthesized MOF-5/BiOBr photocatalyst exhibits better photocatalytic performance than pure MOF-5 and BiOBr under simulated sunlight. The efficiency of Rhodamine B (RhB) removal based MOF-5/BiOBr composite (MOF-5 with mass ratio of MOF-5/BiOBr = 20 wt% of) reached 99.7%. The possible photocatalytic mechanism is discussed through the capture experiment of active species. The enhanced photocatalytic performance of the MOF-5/BiOBr composite may be related to the interaction between BiOBr and MOF-5 and the type II charge transfer path. The catalyst has simple preparation process, low cost, high activity under natural light, and high efficiency, and is expected to play a role in the treatment of environmental wastewater. This work provides a new insight for designing MOF-5 based photocatalyst.
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JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY
·
2021
·Vol. 96
·期 8
·2298-2309
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IF 3.174
Shizi Luo,Xinyan Xiao,Yi Wang,Mingli Lu
BACKGROUND The commonly used RhB dye is a carcinogen that is widely found in environmental matrices and poses a threat to aquatic biota and human health. However, conventional wastewater treatment processes do not effectively remove low concentrations of these pollutants. Herein, the P-Bi 4 O 5 Br 2 /AgI (PBA) heterojunction was synthesized via a polyvinylpyrrolidone (PVP)-assisted solvothermal and precipitation method in this work. RESULTS The photocatalytic efficiency of the PBA heterojunction was evaluated by degrading rhodamine B (RhB) with the irradiation of simulated sunlight. P-Bi 4 O 5 Br 2 /AgI-50 (PBA-50, the mass fraction of AgI in the composite was 50%) composite could degrade 98% RhB under 90 min irradiation of 500 W Xenon lamp, and its pseudo first-order reaction rate constant was 0.04265 min −1 , which was 17.1, 2.16, and 2.94 times higher than that of Bi 4 O 5 Br 2 , P-Bi 4 O 5 Br 2 , and AgI, respectively. Besides, the effects of the dosage of photocatalyst and the anion on the photocatalytic degradation of RhB over PBA-50 were analyzed. CONCLUSION The enhanced photocatalytic activity of PBA was attributed to its better visible light capture ability, larger specific surface area, and faster photogenerated carrier separation efficiency, all of which were confirmed by scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET), UV-Vis diffues reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), and photoelectrochemical analysis. In addition, the free radical trapping experiments confirmed that ·O 2 − and h + were the main active species for degradation of RhB. Additionally, the smaller bandgap and the more negative conduction band position of Bi 4 O 5 Br 2 were reached after the introduction of PVP. Accordingly, a possible type-II heterojunction photocatalytic mechanism of P-Bi 4 O 5 Br 2 /AgI was proposed. © 2021 Society of Chemical Industry (SCI).
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JOURNAL OF POROUS MATERIALS
·
2021
·Vol. 29
·期 1
·181-192
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IF 2.496
Wang Li,Zhou Yu,Xu Qi,Wu Xian-Kun,Xu Guo-Dong,Guo Ji-Xiang,Fang Dong
The development of high efficient and cost-effective photocatalysts for organic matters degradation and hydrogen evolution is of great importance. In this study, heterojunction photocatalysts based In 2 S 3 and MIL-68(In) were synthesized by hydrothermal method. These composites exhibit excellent bi-functionality of photocatalytic Rhodamine B degradation and hydrogen evolution. And it was found that the photocatalytic performance of the composites was dependent on the ratio of In to S. The optimum catalyst In 2 S 3 /MIL-68(In)-1.5 exhibits much enhanced photocatalytic performance, offering a removal efficiency of 94.7% within 30 min for 20 ppm of Rhodamine B and a hydrogen evolution rate of 1618.8 µmol h −1 g −1 as a result of the synergist effect of heterojunction between the two components, promoting the charge separation. Besides, the mechanisms for photocatalytic degradation of Rhodamine B and photocatalytic hydrogen evolution were also proposed. This protocol could provide guiding information on the development of other functional photocatalysts.
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Journal of the Taiwan Institute of Chemical Engineers
·
2021
·
IF 5.876
Xuelian Li,Saleem Raza,Changkun Liu
Photocatalysis, in which carcinogenic compounds are decomposed into harmless products, is the most promising method for the eco-friendly degradation of wastewater pollutants. This study investigated a novel bio-based polymeric microsphere photocatalyst produced via the precipitation polymerization of widely available biomass-derived phenylpropenes trans-anethole (ANE) and N-phenylmaleimide (N-PMI). Amino-modified TiO 2 nanoparticles were grafted onto the surfaces of the microspheres, thereby producing Poly[ANE+N-PMI]-TiO 2 microspheres using photocatalysis. The microspheres were used as photocatalysts for the degradation of rhodamine B (RhB) dye and tetracycline (TC) antibiotics in wastewater, where 95% and 97% degradation rates were achieved for 50 mg·L -1 RhB and 100 mg·L -1 TC, respectively. The microsphere photocatalyst exhibited high stability and recyclability, and maintained excellent photocatalytic performance during continued cycling. Kinetic studies demonstrated that the photocatalytic degradation of RhB and TC proceeded according to a pseudo-first-order kinetics model. Furthermore, superoxide free radicals (·O 2 − ) and hydroxyl radicals (·OH) were the primary and secondary reactive species during photo-degradation. Overall, the excellent performance of the simple TiO 2 -based photocatalyst was clearly demonstrated, and its numerous advantages, such as low energy consumption, low cost, non-toxicity, and environmental friendliness, highlight its promising practical applications.
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Environmental Technology & Innovation
·
2020
·
IF 3.356
Vu Thi Quyen,Le Thi Thu Ha,Dang My Thanh,Quyet Van Le,Nguyen Minh Viet,Nguyen Thi Nham,Phan Quang Thang
Advanced synthesis of nanoflower structures consisting of TiO 2 @Ti 3 C 2 nanoflowers with three-dimensional (3D) porous frameworks from two-dimensional (2D) Ti 3 C 2 MXene was done and applied for degradation of organic pollutant. The special structure of material was created by the in situ transformation, starting from Ti 3 C 2 T x MXene as provision of Ti source. The basis properties of material were characterized by SEM, TEM , XRD and XPS. The Ti 3 C 2 T x MXene showed layered structure and then this morphology was replaced by nanoflower spheres with rapid growth of TiO 2 @Ti 3 C 2 nanowhiskers. In terms of application, the TiO 2 @Ti 3 C 2 heterojunction showed an extraordinary photocatalytic efficiency toward Rhodamine B (RhB) compared to performances of pristine Ti 3 C 2 , and commercial TiO 2 . In addition, the TiO 2 @Ti 3 C 2 composite also displays the good recyclability even after 5th degradation cycles. Based on the finding, it gains a deeper insight into practical applications of 2D transition metal carbide for treatment of organic pollutants in wastewater.
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