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Materials Today Nano · 2023 · IF 10.3

Permselective and transparent wooden membrane with artemisinin-imprinted nanocages based on a MOFs@C3N4 self-assembly design

Jing Yan,Faguang Ma,Yilin Wu

Molecularly imprinted membranes have superior selective separation capacity, rebinding capacity, and flux due to their microporous substrates and tightly packed molecularly imprinted polymers . In current study, artemisinin (Ars), the most effective antimalarial drug , is used as template molecule. The permeation-selectivity wooden membranes based on Ars-imprinted nanocages designed by metal organic framework@carbon nitride self-assembly process (MDWMs) has been successfully prepared: (i) based on three-dimensional mesoporous basswood membranes, dopamine-based auto-polymerization process was developed on basswood to for harvest the first layer imprinting and secondary reaction platform. (ii) The two-dimensional sheet carbon nitride modified by metal-organic framework is stably loaded on the surface of the polydopamine-modified basswood membrane, providing a rich irregular point array structure for the formation of recognition sites. Based on elaborate designs and optimizations, selectivity , rebinding capabilities, and flux are enhanced on the developed MDWMs ( β Are/Ars  = 6.49, β Aru/Ars  = 4.22, β DH-Ars/Ars  = 7.42), and high regeneration rate (>94% after 10 cycles) indicates that MDWMs have superior selectivity and stability. The MDWMs and preparation strategies developed here will provide a completely new design methodology for subsequent selective separation of Ars.

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Greenhouse Gases-Science and Technology · 2023 ·Vol. 13 ·期 5 ·689-698 · IF 2.2

The efficient CO2 fixation catalyzed by K-doped g-C3N4 catalyst for synthesizing benzimidazoles at atmospheric pressure

Xuewei Tu,Luping Zhang,Yutong Chen,Shouxin Zhu,Can Sun,Jiali Jin,Min Liu,Hui Zheng

The conversion of CO 2 into valuable chemicals to reduce greenhouse gas emissions has received extensive attention. Converting CO 2 into pharmaceutical intermediates via graphitic carbon nitride (CN) at atmospheric pressure is a challenge. In this work, a series of novel graphitic carbon nitrides (K-CN) catalysts with different doping ratios of K were synthesized by post-treatment of CN with KOH as a dopant under magnetic stirring. Herein, substrates of o -phenylenediamine with different electron-donating/withdrawing groups were employed to convert CO 2 into high-value heterocyclic benzimidazoles. The optimal reaction conditions were determined by a single factor optimization approach. A series of benzimidazole derivatives were synthesized with a yield of up to 96% under atmospheric pressure, indicating that the catalyst can efficiently fix CO 2 . This work not only designs a simple and low-cost K-CN catalyst but also provides a new pathway for converting CO 2 into valuable benzimidazole derivatives at atmospheric pressure. © 2023 Society of Chemical Industry and John Wiley & Sons, Ltd.

CAS / MDL: 1575-37-7 95-54-5
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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Design of hybrid g-C3N4/GO/MCE photocatalytic membranes with enhanced separation performance under visible-light irradiation

Junyang Pan,Dan Hua,Yiping Hong,Xi Cheng,Fangsong Guo,Kok Bing Tan,Ziqi Zhong,Guowu Zhan

Photocatalytic membranes with concurrent catalytic oxidation and separating functions possess promising potentials for the degradation of organic pollutants in wastewater treatment. Herein, we designed a hybrid photocatalytic membrane ( viz. , g-C 3 N 4 /GO/MCE) by vacuum-filtration-assisted assembling method, consisting of graphitic carbon nitride (g-C 3 N 4 ) nanosheets as a top layer, graphene oxide (GO) nanosheets as an interlayer, and commercial mixed cellulose ester (MCE) as a substrate layer. The microstructures, chemical compositions, and physicochemical properties of the designed g-C 3 N 4 /GO/MCE membranes were systematically characterized by a series of characterization techniques. Particularly, photocatalysis-filtration reactor cells were designed for the evaluation of the simultaneous separation and photocatalytic degradation performance in a single unit using both organic dyes and antibiotics as modeling pollutants in wastewater. Four parameters were adopted to represent the integrated photocatalysis-filtration performance of our designed photocatalytic membranes, including permeance ( P ), rejection ( R’ , filtration alone), removal ( R , combined photocatalysis-filtration under light-irradiation), and degradation rate ( D ). The hybrid membranes showed superior permeance and solute removal under visible-light irradiation (300 W, λ  > 420 nm), in which the permeance was 20% higher than that of no-irradiation conditions. In addition, 10 consecutive cycling tests and light-on/off cycles of the as-prepared g-C 3 N 4 /GO/MCE membrane toward RhB showed quite stable permeance in the range of 268.9 to 352.9 L h −1 m −2 bar −1 , and the removal was maintained in the range of 88.4% to 95.4%, indicating excellent long-term stability. Remarkably, it also exhibited good removal performance of antibiotics ( e.g. , ofloxacin, norfloxacin, sulfamethoxazole, erythromycin, and roxithromycin). Accordingly, the designed hybrid g-C 3 N 4 /GO/MCE photocatalytic membranes with excellent photocatalytic activity and photocatalysis-filtration performance are promising for wastewater treatment and water purification applications.

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Journal of Environmental Chemical Engineering · 2023 · IF 7.7

Visible-light photocatalysis degradation of enrofloxacin by crawfish shell biochar combined with g-C3N4: Effects and mechanisms

Longqu Xiao,Shiyang Zhang,Boqi Chen,Panpan Wu,Ningdong Feng,Feng Deng,Zhi Wang

Herein, a new type of photocatalyst, that is biochar/g-C 3 N 4 (BC/CN) composite, was successfully prepared from melamine and waste crawfish shells by a simple thermal condensation process and used to degrade enrofloxacin (ENR) wastewater under visible light. The structure and photoelectrochemical properties of the composites were thoroughly characterized. Results showed that there are obvious synergistic effects between BC and CN present in the composite. When the ratio of BC to CN is 2%, the catalyst (BC/CN-2%) has the best visible-light photocatalytic performance. The •O 2 − radicals were the main oxidation free radicals responsible for ENR removal and the radicals first attacked the piperazine moiety of the ENR, and further, the whole photocatalytic degradation pathway was proposed. This study provided a promising strategy for the synthesis of photocatalyst materials from waste crawfish shells and their application in the treatment of antibiotic wastewater.

CAS / MDL: 75-65-0 68649-12-7
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RSC Advances · 2023 ·Vol. 13 ·期 12 ·8383-8393 · IF 3.9

Photocatalytic degradation of tetracycline hydrochloride by lanthanum doped TiO2@g-C3N4 activated persulfate under visible light irradiation

Yan Wang,Jingyu Xiu,Tao Gan,Haiming Zou,Feiyue Li

In this work, a visible light-driven La/TiO2@g-C3N4 photocatalyst was synthesized for the photodegradation of tetracycline hydrochloride (TCH) in the presence of peroxydisulfate (PDS) in an internal loop-lift reactor. The surface morphology and structure of La/TiO2@g-C3N4 have been characterized by XRD, SEM-EDS, FTIR, XPS, and UV/vis DRS. La/TiO2@g-C3N4 displays outstanding photocatalytic performance and reusability. After four reuse cycles of the vis/La/TiO2@g-C3N4/PDS system, the TCH degradation rate and efficiency still reached 0.083 min−1 and 97.68%, respectively. Reactive species in this system included free radicals SO4˙−, ˙OH, and ˙O2−, as well as non-radicals e−, and h+, as established from the results of chemical quenching experiments. Moreover, a mechanism of action of the vis/La/TiO2@g-C3N4/PDS system for TCH degradation was proposed. The acute toxicity of the reaction solution towards Photobacterium phosphoreum T3 spp. in the vis/La/TiO2@g-C3N4/PDS process increased during the first 60 min and then decreased, illustrating that vis/La/TiO2@g-C3N4/PDS provided an effective and safe method for the removal of TCH.

CAS / MDL: 3317-61-1 2403-88-5
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MOLECULES · 2023 ·Vol. 28 ·期 6 ·2647 · IF 4.6

Removal of Tetracycline Hydrochloride by Photocatalysis Using Electrospun PAN Nanofibrous Membranes Coated with g-C3N4/Ti3C2/Ag3PO4

Peng Wang,Xu Han,Xianhong Zheng,Zongqian Wang,Changlong Li,Zhiqi Zhao

In order to improve the photocatalytic performance of g-C3N4, the g-C3N4/Ti3C2/Ag3PO4S-type heterojunction catalyst was prepared by electrostatic assembly method, and then the g-C3N4/Ti3C2/Ag3PO4/PAN composite nanofiber membrane was prepared by electrospinning technology. The morphology and chemical properties of the nanofiber membrane were characterized by SEM, FTIR, and XRD, and the photocatalytic degradation of tetracycline hydrochloride (TC) in water by the nanofiber membrane was investigated. The results showed that g-C3N4/Ti3C2/Ag3PO4could be successfully loaded on PAN and uniformly distributed on the surface of composite nanofiber membrane by electrospinning technology. Increasing the amount of loading and catalyst, lowering the pH value and TC concentration of the system were conducive to the oxidation and degradation of TC. The nano-fiber catalytic membrane had been recycled five times and found to have excellent photocatalytic stability and reusability. The study of catalytic mechanism showed that h+, •OH and •O2−were produced and participated in the oxidation degradation reaction of TC, and •O2−plays a major role in catalysis. Therefore, this work provides a new insight into the construction of high-performance and high-stability photocatalytic system by electrospinning technology.Keywords:photocatalytic;PAN nanofiber membrane;degradation;tetracycline;heterojunction

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JOURNAL OF ENVIRONMENTAL MANAGEMENT · 2023 · IF 8.7

Constructing C–O bridged CeO2/g-C3N4 S-scheme heterojunction for methyl orange photodegradation:Experimental and theoretical calculation

Chen Yang,Jian Yang,Shuangshuang Liu,Mingxue Zhao,Xu Duan,Hongli Wu,Lang Liu,Weizao Liu,Jiangling Li,Shan Ren,Qingcai Liu

Owing to its feasibility, efficiency in light-harvesting and effectiveness in the interfacial charge transfer between two n-type semiconductors, constructing heterojunction photocatalysts have been identified as an effective way for enhancing the photocatalytic properties. In this research, a C–O bridged CeO 2 /g-C 3 N 4 (cCN) Step-scheme (S-scheme) heterojunction photocatalyst was constructed successfully. Under visible light irradiation, the cCN heterojunction exhibited the photocatalytic degradation efficiency of methyl orange, which was about 4.5 and 1.5 times higher than that of pristine CeO 2 and CN, respectively. The DFT calculations, XPS and FTIR analyses demonstrated the formation of C–O linkages. And the calculations of work functions revealed the electrons would flow from g-C 3 N 4 to CeO 2 due to the difference in Fermi levels , resulting in the production of internal electric fields . Benefiting from the C–O bond and internal electric field, the photo-induced holes in the valence band of g-C 3 N 4 and the photo-induced electrons from conduction band of CeO 2 would be recombined when exposed to visible light irradiation, while leaving the electrons with higher redox potential in the conduction band of g-C 3 N 4 . This collaboration accelerated the separation and transfer rate of photo-generated electron-hole pairs, which promoted the generation of superoxide radical (•O 2 − ) and improved the photocatalytic activity .

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APPLIED SURFACE SCIENCE · 2023 · IF 6.7

Efficient degradation of ciprofloxacin by Cu2O/g-C3N4 heterostructures with different morphologies driven under the visible light

Jing Chen,Haitao Zhu,Qifang Ren,Shaohua Chen,Yi Ding,Zhen Jin,Wanmi Guo,Xinyu Jia

In this study, Cu 2 O/g-C 3 N 4 composite with photocatalytic activity was successfully prepared by chemical precipitation method. The catalytic degradation of ciprofloxacin (CIP) by Cu 2 O and Cu 2 O/g-C 3 N 4 composites with different morphologies was investigated. The effective structure and properties of Cu 2 O/g-C 3 N 4 composites were tested by a series of characterization methods. The photocatalytic test results show that the Cu 2 O/g-C 3 N 4 composite photocatalyst has good stability and good photocatalytic performance, which is attributed to the effective hetero-junction structure formed by the combination of Cu 2 O and g-C 3 N 4 , which promotes the interfacial charge separation. The addition of g-C 3 N 4 can reduce the crystal size of Cu 2 O, improve the crystal morphology, and increase its light utilization. Among the synthesized catalysts, the Cu 2 O-3(20%)/g-C 3 N 4 composite has the highest catalytic activity, and the photocatalytic oxidation efficiency of CIP is 96%. By free radical capture and ESR analysis, it was verified that OH, h + and O 2 − radicals may be the main active substances involved in CIP photodegradation. Finally, various degradation products and intermediates of CIP were identified by LC-MS, and the possible conversion pathways were proposed.

CAS / MDL: 6046-93-1
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NANO · 2023 · IF 1.2

Preparation of g-C3N4/TiO2 Heterojunction Composite Photocatalyst by NaCl Template Method and Its Photocatalytic Performance Enhancement

Yong Li,Manyu Liu,Mingqing Zhang,Yanfang Liu,Qinghua Zhao,Xin Li,Qianyu Zhou,Yuanfu Chen,Shifeng Wang

Photocatalytic technology is currently the most promising technology for environmental pollution control. The preparation of photocatalysts with excellent properties is the core of the development of photocatalytic technology. TiO 2 can form a heterojunction with g-C 3 N 4 , which can effectively inhibit the recombination of photogenerated electron–hole pairs, improve the mobility of photogenerated carriers, and thus improve the photocatalytic performance. In this study, NaCl was used as a template, and the loose and porous g-C 3 N 4 /TiO 2 heterojunction composite photocatalysts were prepared by the template method. Compared to the pure g-C 3 N 4 prepared by the conventional thermal polycondensation method and TiO 2 , the g-C 3 N 4 /TiO 2 heterojunction composite photocatalysts prepared in this study exhibited a greatly increased specific surface area, an improved light absorption performance, a significantly suppressed recombination of photogenerated electrons and holes. Furthermore, the g-C 3 N 4 /TiO 2 heterojunction composite photocatalysts exhibited excellent photocatalytic performance.

CAS / MDL: 7647-14-5 108-78-1
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Catalysis Science & Technology · 2023 ·Vol. 13 ·期 3 ·898-909 · IF 5

N-doped rutile TiO2 nanorod@g-C3N4 core/shell S-scheme heterojunctions for boosting CO2 photoreduction activity

Haohui Gu,Feng Liang,Xiaohan Wang,Shuaibing Wu,Gongye Lv,Haijun Zhang,Shaowei Zhang,Lilin Lu,Zhijun Dong

The design of heterojunction photocatalysts is regarded as a very effective method to solve the high recombination rate of photogenerated charge carriers for CO2 photoreduction into hydrocarbons, and interface engineering is urgently required to achieve high efficiency. Herein, graphitic carbon nitride (g-C3N4, CN) was uniformly grown on the surface of nitrogen-doped rutile TiO2 (NT) nanorods by in situ deposition, and a NT@CN core/shell step-scheme (S-scheme) heterojunction system composed of NT nanorods and g-C3N4 was synthesised. The as-synthesised heterojunction containing 55 wt% g-C3N4 delivered the highest CO2 photoreduction activity (33.35 μmol g−1 for CO) without additional cocatalysts or external sacrificial agents, which was 7.1 times higher than that of bare NT nanorods. This improved CO2 reduction activity was attributable to the large surface area and impactful S-scheme heterostructure, which imparted the catalyst with sufficient visible-light harvesting ability, promoted the segregation and transformation of the photoinduced charge pairs, and enhanced the redox ability of the carriers. Concurrently, the NT@CN photocatalyst exhibited excellent reusability and stability. This work offers a new basis for designing and preparing rutile TiO2-based S-scheme heterojunctions with enhanced CO2 reduction performance.

CAS / MDL: 108-78-1 57-13-6
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Journal of Environmental Chemical Engineering · 2022 · IF 7.968

Visible-light-driven Ag3VO4-BiVO4/C3N4 with continuous type II heterojunctions for effective removal of Cr(VI)

Qi Wang,Biao Xue,Meng Tan,Ningyi Li,Hao Zhou,Hao Du,Guoxiang Yang,Huaze Zhu,Qiang Li

Heterogeneous photocatalysis have attracted extensive attention in the field of environmental remediation. The low charge separation efficiency and poor light response of single semiconductor can be remarkably improved through forming heterojunction . The construction of ternary heterojunctions can further inhibit the recombination of photogenerated charge carriers by the separated redox active sites. A novel and highly efficient Ag 3 VO 4 -BiVO 4 /C 3 N 4 ternary heterojunction were successfully synthesized and characterized in terms of structure, chemical composition and photocatalytic properties. The photocatalytic activities of as-synthesized photocatalysts were evaluated by the photocatalytic reduction of Cr(VI) in the aqueous solution. The photocatalytic Cr(VI) reduction rate of ternary heterojunction is 19 times higher than that by single BiVO 4 . The lower pH, higher concentration of coexisted organics and stronger light intensity endowed photocatalysts with better photocatalytic performance. More Cr(VI) ions were remained in the solution with higher initial concentration of Cr(VI) under the same light irradiation. The Cr(VI) ions could also be totally removed by the ternary heterojunction even after five cycling tests showing good cycling stability. The internal electric field between Ag 3 VO 4 , BiVO 4 and graphitic carbon nitride (C 3 N 4 ) facilitated the separation of photogenerated electron/hole pairs. The suitable band alignments endow ternary heterojunction with isolated oxidation and reduction reactions due to the separated holes and electrons, meanwhile, suppressing charge carrier recombination. This research provides guidance for the rational design of multi-components heterojunction for photocatalytic environmental remediation.

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MICROCHIMICA ACTA · 2018 ·Vol. 185 ·期 12 ·1-8 · IF 5.705

Photoelectrochemical determination of the activity of protein kinase A by using g-C3N4 and CdS quantum dots

Sui Chengji,Liu Fei,Tang Lihua,Li Xue,Zhou Yunlei,Yin Huanshun,Ai Shiyun

A sensitive and selective photoelectrochemical (PEC) method is described for the detection of protein kinase A (PKA) activity based on the use of graphite-like carbon nitride (g-C 3 N 4 ) and the CdS quantum dots (QDs). Firstly, a complex was synthesized from g-C 3 N 4 and gold nanoparticles (AuNPs). It was employed as both the PEC-active material and as a support for immobilization of peptides. The latter were assembled on an ITO electrode modified with g-C 3 N 4 -AuNPs and subsequently phosphorylated by PKA in the presence of adenosine 5′-[γ-thio]triphosphate (ATP-S). Finally, CdS quantum dots (QDs) were introduced on the ITO in order to increase the PEC response of g-C 3 N 4 based on the Cd-S binding between the QDs and thiol groups. Under the optimal conditions and a typical working voltage of −0.3 V, the method has a dynamic range that extends from 0.05 to 50 unit·mL −1 , with a 0.017 unit·mL −1 lower detection limit. The method was successfully applied to the quantification of the inhibitory effect of ellagic acid on the activity of PKA, and to monitor enzyme activity in cell lysates. Schematic of a sensitive and selective photoelectrochemical biosensor for the detection of protein kinase A activity. It is based on the use of graphite-like carbon nitride and CdS quantum dots.

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