TALANTA
·
2017
·
IF 4.162
Xuemei Wang,Pengfei Huang,Xiaomin Ma,Huan Wang,Xiaoquan Lu,Xinzhen Du
Novel magnetic mesoporous molecularly imprinted polymers (MMIPs) with core-shell structure were prepared by simple surface molecular imprinting polymerization using tetrabromobisphenol-S (TBBPS) as the template. The MMIPs-TBBPS were characterized by fourier-transform infrared spectrometry (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), N 2 adsorption-desorption transmission, and vibrating sample magnetometry . The resultant MMIPs-TBBPS were successfully applied magnetic solid-phase extraction (MSPE) coupled with HPLC determination of TBBPS in spiked real water samples with recoveries of 77.8–88.9%. The adsorption experiments showed that the binding capacity of MMIPs-TBBPS to TBBPS and six structural analogs were significantly higher than that of the magnetic nonimprinted polymers (MNIPs). Meanwhile, the MMIPs-TBBPS possessed rapid binding affinity , excellent magnetic response, specific selectivity and high adsorption capacity toward TBBPS with a maximum adsorption capacity of 1626.8 µg g −1 . The analytical results indicate that the MMIPs-TBBPS are promising materials for selective separation and fast enrichment of TBBPS from complicated enviromental samples.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2025
·
IF 9.7
Jie Zhang,Chengcheng Yuan,Yong Zhang,Changhong Sun,Jiaguo Yu,Liuyang Zhang
Photocatalytic hydrogen peroxide production offers a greener alternative, but its efficiency is limited by high carrier recombination. Covalent organic frameworks, with their highly ordered structures and tunable properties, are promising photocatalysts. However, their application in H 2 O 2 production has been constrained by the lack of effective strategies to enhance catalytic activity. In this study, BiOCl/COF (TFPB-BPY) S-scheme heterojunctions were prepared via a simple in-situ growth method. The heterojunction exploits the nitrogen-rich architecture and charge transport of the COF, combined with the broad light absorption and internal electric field of BiOCl. This synergy enables superior visible light absorption, efficient charge separation, and suppressed recombination. Mechanistic studies confirmed the S-scheme mechanism as the key to its enhanced performance. This work provides a scalable and eco-friendly strategy for improving COF-based photocatalysts through S-scheme heterojunctions, offering a pathway for sustainable H 2 O 2 production and advancing the rational design of photocatalysts for green energy applications.
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Journal of Building Engineering
·
2024
·
IF 6.7
Baomin Wang,Weigao Ding,Chengcheng Fan,Fei Liu,Wenxin Lu,Haoxiang Yang
C-S-H gel is a complex cementitious system, and the properties present significant difference with various Ca/Si ratios. The immobilization mechanism of three heavy metals in C-S-H gel at various Ca/Si ratios was investigated in this work from the prospect of the physical adsorption and chemical immobilization. Results showed that higher Ca/Si ratios can result in an increase in silicon chain polymerization, and lower BET specific area, and C-S-H gel with various Ca/Si ratios showed the excellent immobilization for heavy metals. Pb(II) and Zn(II) can form hydroxyl complex polyhedra in C-S-H under strongly alkaline environments, and increase the silicon chain polymerization degree similar to the doping of C-S-H gel by Al. However, Cd(II) was immobilized in the C-S-H gel with the formation of a solid solution under the action of ion exchange with Ca(II), rather than in the form of hydroxyl complex polyhedral and cadmium hydroxide coprecipitates. The highest adsorption capacity of Pb(II) was realized in C-S-H gel with a Ca/Si molar ratio of 0.9, reaching 95.6006 mg/g. Pb(II) was mainly immobilized in C-S-H gel via physical and chemical adsorption, and the effect of chemical adsorption tended to be significant as the Ca/Si molar ratio increased. And the formation of Pb 8 Ca(Si 2 O 7 ) 3 can be detected in C-S-H gel with a higher Ca/Si molar ratio.
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JOURNAL OF ENVIRONMENTAL MANAGEMENT
·
2025
·
IF 8.4
Jiayi Wang,Penggang Ren,Ying Zhang,Zihang Cai,Zhengyan Chen,Yanling Jin,Zhengzheng Guo
BiOI is a promising photocatalyst due to its exceptional visible light response and high absorption coefficient; however, its performance is hindered by the rapid recombination of electron-hole (e − -h + ) pairs. Herein, a 2D/3D BiOI/g-C 3 N 4 S-scheme heterojunction catalyst was designed and constructed through the alkali etching strategy and subsequent microwave-assisted hydrothermal strategy. The abundant surface active sites and matched band gap of g-C 3 N 4 prepared through alkali etching facilitates anchoring of BiOI nanosheets, contact with contaminants and construction of heterojunctions. 2D/3D S-scheme heterojunction substantially promote electron-hole (e − -h + ) pairs separation and transfer. Profited from their synergistic effects, the 2D/3D BiOI/g-C 3 N 4 heterojunction delivers superior photocatalytic activity toward four different types of pollutants: methylene blue (91.7 %), tetracycline (91.9 %), eosin y (90.9 %) and methyl orange (97.7 %), and demonstrates excellent cyclic stability after seven methylene blue cyclic degradation experiments. Furthermore, BiOI/g-C 3 N 4 has shown satisfactory practicability in many simulation experiments, such as coexisting cations, different pH and real water. A feasible strategy to prepare a visible-light-driven multidimensional coordinated S-scheme heterojunction photocatalyst is provided in this work.
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SURFACE & COATINGS TECHNOLOGY
·
2025
·
IF 6.1
Zhipeng Xie,Lu Wang,Yuhui Cheng,Qian Guo,Haibo Zhou,Congshu Huang,Jingjing Wang,Weifeng Bu
Improving the performance of antifouling coating under illumination-involved harsh environments is of prime scientific and engineering importance. However, it still remains a big challenge due to the strong photo-corrosion character of cuprous oxide (Cu 2 O) that works as the most widely-used primary antifoulant. To address this issue, a novel heterojunction of Cu 2 O@TiO 2 was constructed by in situ adsorption-hydrolysis approach. The as-designed heterojunction structure endows superior photo-stability with Cu 2 O@TiO 2 , which has been proven to proceed via S-scheme mechanism by a set of complementary characterizations including in situ XPS and EPR. As anticipated, the resulted Cu 2 O@TiO 2 coating manifests excellent stability and antifouling performance under illumination-involved mimetic service conditions such as dry-dock and waterline environments, as substantiated by the bioassays and marine field trials. A dual-target photo-synergized enhancing mechanism for the S-scheme Cu 2 O@TiO 2 could be deduced as to: (i) inhibit the accumulation of holes on Cu 2 O to exert a stabilization effect; (ii) boost the generation of reactive oxygen species (ROS, including HO /O 2 − ) to enhance the antifouling property. The methodology provides a proof-of-concept design to fabricate high photo-stable Cu 2 O-based antifoulant materials, with the gain in understanding the intrinsic failure principle of coatings and the biocidal mechanism of cuprous oxide toward marine application.
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JOURNAL OF ORGANIC CHEMISTRY
·
2025
·
IF 3.6
Jiaxuan Dong,Yifan Lv,Yiyang Li,Kexin Xu,Xinrui Cui,Cun-Yue Guo,Baolin Li
Thienoacenes are a prominent class of fused-ring conjugated organic compounds and have attracted considerable attention due to their high coplanarity, good stability, high charge-carrier mobility, etc. However, most current synthetic methods toward thienoacenes require costly starting materials and reagents, as well as a lengthy synthetic procedure with low overall yields. Herein, a nonprecious copper-catalyzed system without additional ligands was developed to facilitate C–S coupling and 5-endo-dig thienannulation reaction, leading to the synthesis of a range of thienoacenes including dithieno[3,2-b:2′,3′-d]thiophenes (DTTs) and thieno[2′,3′:4,5]thieno[3,2-b]thiophene[2,3-d]thiophene (TTAs) with yields of up to 90% (for single-sided thienannulation reactions) and 65% (for double-sided thienannulation reactions). In addition, three π-extended DTTs were studied as potential thermoelectric materials, and their composites with single-walled carbon nanotubes (SWCNTs) exhibited high thermoelectric performance with the power factor up to 399.01 ± 16.26 μW m–1 K–2 at room temperature, which is the highest reported for thermoelectric composites comprising small-molecule thiophene derivatives and SWCNTs, signifying a step forward in the development of high-performance thermoelectric composites based on thiophene derivatives.
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ENZYME AND MICROBIAL TECHNOLOGY
·
2014
·
IF 2.966
Xue-Qing Yang,Ya-Lin Zhang
Glutathione S -transferases (GSTs) play a key role in detoxification of xenobiotics in organisms. However, their other functions, especially response to the natural toxin cantharidin produced by beetles in the Meloidae and Oedemeridae families, are less known. We obtained GST cDNAs from three sources: Cydia pomonella ( CpGSTd1 ), Sus scrofa ( SsGSTα1 ), and Triticum aestivum ( TaGSTf3 ). The predicted molecular mass is 24.19, 25.28 and 24.49 kDa, respectively. These proteins contain typical N-terminal and C-terminal domains. Recombinant GSTs were heterologously expressed in Escherichia coli as soluble fusion proteins. Their optimal activities are exhibited at pH 7.0–7.5 at 30 °C. Activity of CpGSTd1 is strongly inhibited by cantharidin and cantharidic acid, but is only slightly suppressed by the demethylated analog of cantharidin and cantharidic acid. Enzymatic assays revealed that cantharidin has no effect on SsGSTα1 activity, while it significantly stimulates TaGSTf3 activity, with an EC 50 value of 0.3852 mM. Activities of these proteins are potently inhibited by the known GST competitive inhibitor: S -hexylglutathione (GTX). Our results suggest that these GSTs from different sources share similar structural and biochemical characteristics. Our results also suggest that CpGSTd1 might act as a binding protein with cantharidin and its analogs.
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HIGH PERFORMANCE POLYMERS
·
2020
·
IF 1.568
Yan Chen,Fajian Ren,Jian gang Dai,Dongmei Li,Shajie Luo
A series of modified poly(ether ether ketone)s containing different content of benzene pendant group in the molecular chain have been successfully synthesized with 1,1-bis(4-hydroxyphenyl)-1-phenylethane, bisphenol A and 4,4′-difluorobenzophenone by nucleophilic substitution. The inherent viscosities of obtained polymers were in the range of 0.261–0.889 dLg−1. They were found to have high glass transition temperatures (Tg) of 150–168°C and 148–169°C (examined by DSC and DMA, respectively), good thermal stability with 5% weight-loss temperature (T5%) of 439–469°C. The tensile strengths of the obtained polymers were 67.7–86.6 MPa, and the storage modulus was over 0.9 GPa at about 140°C. The modified poly(ether ether ketone)s showed the excellent solubility property, they could be processed by solution method. Additionally, the obtained polymers had good optical transmittance (>70%) at 400 nm, suggesting that they have potential to be applied to the heat-resistant optical films.
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Energy Storage Materials
·
2020
·
IF 16.28
Muhammad Waqas,Yupei Han,Dongjiang Chen,Shamshad Ali,Cheng Zhen,Chao Feng,Botao Yuan,Jiecai Han,Weidong He
With high energy density and low cost, lithium sulfur (Li–S) batteries own the potential to be next-generation electrochemical storage/conversion devices. However, their cyclic stability and life span are considerably impaired by polysulfide shuttling and self-discharge. Here, we design a microfiber glass filter-molybdenum disulfide/carbon-titanium nitride (μFGF-MoS 2 /C–TiN) interlayer for suppressing the shuttle of polysulfides and self-discharge of Li–S batteries. TiN in the interlayer molecularly captures high-order polysulfide Li 2 S 8 with an adsorption energy up to −6.48 eV, the largest high-order polysulfide absorption value ever reported. The μFGF-MoS 2 layer mechanically seizes polysulfides with interconnected torturous mesopores by functioning as a molecular sieve . With a sulfur loading of 4.5 mg cm −2 , the Li–S batteries based on μFGF-MoS 2 /C–TiN exhibit remarkable over-1000-cycle stability with an only 0.05% capacity decay per cycle and deliver an initial discharge capacity of 1000 mAh g −1 at 1C. The self-discharge is alleviated with an insignificant 10.3% capacity loss after a 30-day rest.
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2020
·
IF 3.232
Xiupei Yang,Dan Wang,Na Luo,Min Feng,Xiaohui Peng,Xiangjun Liao
A simple and green approach for the synthesis of photoluminescent N,S-carbon dots (N,S-CDs) has been proposed using a single natural source precursor (bamboo leaf) as raw materials. The as-synthesized N,S-CDs exhibited a highly stable, excitation wavelength-dependent emission, excellent photobleaching, alkali, and salt tolerance. Here, the mechanism of N,S-CDs luminescence was studied via the UV–vis absorption spectrum and photoluminescence spectroscopy . Based on the quenching properties of nitrophenol compounds on the fluorescence of N,S-CDs, the interaction between N,S-CDs and nitrophenol compounds was investigated on detail in aqueous solution. More importantly, the study on photophysical properties of the N,S-CDs may provide the basis for the development of the N,S-CDs for the fluorescent probe of nitrophenol compounds.
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CHEMOSPHERE
·
2020
·
IF 5.778
Chu-Ya Wang,Qi Zeng,Guangcan Zhu
Bisphenol A (BPA), a typical endocrine disrupting chemical, is widespread in aqueous environment and cannot be efficiently treated by traditional water treatment technologies . Bismuth oxybromide (BiOBr) is a promising photocatalyst with a special layered structure. However, its band gap (2.8 eV) is not narrow enough for the efficient harvesting of visible light, severely restricting its practical use. Given that the band gap of Bi 2 S 3 is only 1.3 eV, S-doping modification could be used to tailor the band structure of BiOBr. Here, series of S-doped BiOBr nanosheets was prepared through a facile hydrothermal procedure. The as-prepared S 0.2 -BiOBr nanosheets showed a narrower band gap of 2.33 eV. The intrinsic photocatalytic activity of S 0.2 -BiOBr sample for the degradation of BPA was 2.78 times higher than that of BiOBr under visible light degradation. Moreover, the mechanism of BPA degradation over the S-doped BiOBr under visible light irradiation was elucidated based on the experimental results and density functional theoretical calculations. Overall, a feasible and effective doping method was proposed to improve the utilization efficiency of visible light.
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RSC Advances
·
2017
·Vol. 7
·期 47
·29378-29385
·
IF 3.108
Leyan Nian,Junben Huang,Kui Wu,Zhi Su,Zhihua Yang,Shilie Pan
Five non-centrosymmetric (NCS) quaternary metal chalcogenides, BaCu2SiSe4, BaCu2GeS4, BaCu2GeSe4, BaCu2SnS4, and BaCu2SnSe4, were successfully synthesized by solid-state reaction in vacuum-sealed silica tubes. They crystallized in the three different space groups: Ama2 for BaCu2SnSe4, P3121 for BaCu2GeS4 and BaCu2GeSe4, and P3221 for BaCu2SiSe4 and BaCu2SnS4. Note that BaCu2GeS4 and BaCu2GeSe4 show the mirror symmetrical structures to those of BaCu2SiSe4 and BaCu2SnS4. In comparison with their structures, it can be found that the [CuSe4] units are connected together to form a two-dimensional (2D) layer structure in BaCu2SnSe4, which is different from the 3D framework structure formed by the interlinked [CuQ4] (Q = S and Se) units in other four title compounds. In addition, BaCu2SnSe4 exhibits only one type of tunnel structure with the isolated [BaSe8] units existing in each tunnel, which is also different from the other title compounds (two types of tunnels with the isolated [BaSe8] units and [BaSe6]n chains located). The interesting structural changes also indicate that slight change of cation size would result in different structure features, and future structure prediction should devote considerable attention to the different chalcogen atoms. Moreover, important optical properties (optical bandgap, infrared (IR) absorption edge, second harmonic generation (SHG) response) of the title compounds were systematically investigated. Among them, IR and Raman spectra indicate that all of them exhibit the wide IR absorption edges (∼22 μm). Powder SHG measurement shows that BaCu2SnS4 possesses good SHG response about 1.6 times that of benchmark AgGaS2 (AGS) at the particle size 55–88 μm. All results indicate that BaCu2SnS4 can be expected as a potential IR nonlinear optical (NLO) candidate. Theoretical calculation was also used to analyze the structure–property relationship and their electronic structures and origin of NLO effect were studied in detail.
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