FISH & SHELLFISH IMMUNOLOGY
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2020
·
IF 0
Xiaorong Xu,Kai Liao,Peng Shi,Jilin Xu,Zhaoshou Ran,Chengxu Zhou,Lin Zhang,Jiayi Cao,Xiaojun Yan
Bivalve lectins perform a crucial function in recognition of foreign particles, such as microalgae and pathogenic bacteria. In this study, a novel C-type lectin form Sinonovacula constricta ( ScCL ) was characterized. The full-length cDNA of ScCL was 1645 bp, encoding a predicted polypeptide of 273 amino acids with one typical carbohydrate-recognition domain. ScCL has the highest similarity and closest phylogenetic relationship with the C-type lectin from Solen grandis . Real-time PCR analysis showed that ScCL was expressed in all tested tissues, with the highest expression in the foot and the lowest expression in hemocytes . Agglutination activity of ScCL was Ca 2+ -independent. ScCL showed the strongest agglutination on Chlorella vulgaris , the modest agglutination on Platymonas subcordiformis , Nannochloropsis sp., and Thalassiosira pseudonana , the weakest agglutination on Chaetoceros sp., and no agglutination on Isochrysis zhanjiangensis . Meanwhile, agglutination tests and western blot analysis revealed that the recombinant ScCL protein could agglutinate Staphylococcus aureus and Vibrio harveyi , but could not agglutinate Vibrio anguillarum , Bacillus cereus , or Vibrio parahaemolyticus . Furthermore, ScCL had a high binding activity with LPS and mannose , a low binding activity with LTA, and no binding activity with PGN. The expression of ScCL in the gill of S. constricta fed with C. vulgaris and T. pseudonana was significantly increased at 1 and/or 3 h. After injection with S. aureus , the expression of ScCL in the gill was significantly increased at 3, 6, and 24 h. These results indicated that ScCL was involved in food particle recognition and immunity of S. constricta .
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MOLECULES
·
2020
·Vol. 25
·期 11
·2475
·
IF 3.267
Yanliang Yang,Dexi Yang,Chi Zhang,Min Zheng,Ying Duan
The development of a simple and durable catalytic system for the production of chemicals from a high concentration of a substrate is important for biomass conversion. In this manuscript, 5-hydroxymethylfurfural (HMF) was converted to 1-hydroxy-2,5-hexanedione (HHD) using the combination of commercial Pd/C and acetic acid (AcOH) in water. The influence of temperature, H2pressure, reaction time, catalyst amount and the concentration of AcOH and HMF on this transformation was investigated. A 68% yield of HHD was able to be obtained from HMF at a 13.6 wt% aqueous solution with a 98% conversion of HMF. The resinification of intermediates on the catalyst was characterized to be the main reason for the deactivation of Pd/C. The reusability of the used Pd/C was studied to find that most of the activity could be recovered by being washed in hot tetrahydrofuran.Keywords:HMF;1-hydroxy-2,5-hexanedione;acetic acid;Pd/C;high concentration
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高影响因子
Journal of Materials Chemistry B
·
2020
·Vol. 8
·期 32
·7160-7165
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IF 5.344
Tao Hu,Kangkai Xu,Shanhu Qiu,Yu Han,Juan Chen,Jian Xu,Ke Chen,Zilin Sun,Hong Yi,Zhonghua Ni
A sensitive fluorescent microfluidic sensor based on carbon quantum dots (CQDs), cadmium telluride quantum dots (CdTe QDs) aerogel and glucose oxidase (GOx) for urinal glucose detection was fabricated via a simple method. CQDs, emitting green fluorescence (emission peak at 520 nm) and the CdTe QDs, emitting red fluorescence (emission peak at 620 nm) under 365 nm ultraviolet irradiation, were synthesized. The as-prepared CQDs, CdTe QDs and GOx (C/CdTe QD-GOx) were mixed in a certain ratio and were then introduced into the microfluidic chip to construct a three-dimensional porous aerogel sensor after freeze-drying. A ratiometric fluorescence response was realized through the quenching of the red fluorescence by H2O2 produced from the glucose/GOx reaction, while the green fluorescence intensity stays constant. A small change in the ratio of the two fluorescence intensities led to a clear change in the fluorescent colour of the sensor, which can be easily observed under a UV lamp. The microsensor displayed a serial colour change from red to green with the changes in glucose concentration. The intensity ratio between the red fluorescence and green fluorescence (R/G value) indicates the glucose concentration. In our experiments, the optimal concentration ratio of CdTe QDs and CQDs was 0.5 : 1, and the optimal response time was 5 min. The detection range of glucose concentration was from 0 mM to 13 mM, and the detection limit was 0.223 mM. We also found that this glucose sensor has excellent selectivity, specificity and stability. The as-prepared microsensor can be stably stored for 30 days under −20 °C. Such a C/CdTe QD-GOx aerogel based microfluidic assay sensor provides a new approach towards the optical and quantitative detection of glucose, which enables daily urine glucose monitoring for the diabetic patients in a convenient way.
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高影响因子
RSC Advances
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2020
·Vol. 10
·期 54
·32309-32322
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IF 3.119
Fahim A. Qaraah,Samah A. Mahyoub,Abdo Hezam,Wei Zhang,Guangli Xiu,Janvier Munyaneza,Chengzi Wu
Significant endeavors have been devoted in the past few years to establish efficient visible light-activated photocatalysts. Herein, we successfully synthesized a flower-like hierarchical nitrogen-doped and carbon-sensitized Nb2O5 (NBO) nanostructure (denoted N-NBO/C). The as-prepared N-NBO/C possessed a specific surface area of 260.37 m2 g−1 and single wire diameter of less than 10 nm. The effect of reaction parameters such as hydrothermal reaction time, temperature and concentration of hexamethylenetetramine (Hmta) on the morphology of NBO was systematically investigated to elucidate the growth mechanism. The carbon on the surface and the nitrogen in the framework of NBO are beneficial for light harvesting, visible light absorption, formation of oxygen vacancies, and electron–hole separation. The photocatalytic performance of the as-fabricated N-NBO/C nanostructures was estimated via the photodegradation of 30 mg L−1 RhB, where greater than 98% of RhB was decomposed within 30 min upon visible-light radiation. Hence, the obtained N-NBO/C nanostructure exhibits much higher photocatalytic activity for the decomposition of RhB upon visible light irradiation than that of pure niobium oxide (NBO), nitrogen-doped titanium oxide (N-TIO), and nitrogen-doped niobium oxide (N-NBO). This work supplies a versatile route for the synthesis of nitrogen-doped and carbon-sensitized metal-oxide nanostructures for possible utilization in solar energy transformation and environmental remediation.
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高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
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2020
·
IF 5.774
Yiwen Luo,Xue Huang,Yan Li,Yuqi Fu,Ziyou Wang,Jinfeng Lu,Jing Zhang
In this study, calcined Cu-based metal-organic frameworks impregnated with nickel nitrate and pyrrole (CuNiN@C) with better stability and degradation performance was synthesized by doping of both Ni and N. Coupling with peroxymonosulfate (PMS), CuNiN@C worked as adsorptive bifunctional catalyst in effectively degradation of norfloxacin (NFX). Scanning electron microscopy (SEM) with energy dispersive X-ray spectrometry (EDS), transmission electron microscope (TEM), Selected area electron diffraction (SAED), High resolution transmission electron microscope (HRTEM) and X-ray diffraction (XRD) were applied for the preliminary characterization of the synthesized material to reveal the complete retention of the octahedral particle shape and successful doping of nitrogen. The results showed that over 80% NFX (5 mg/L) was degraded in 30 min with CuNiN@C (0.2 g/L) and PMS (2 mmol/L), and the reusability of CuNiN@C in four cycles did not significantly deteriorated, which was attributed to Ni doping. The mechanism of NFX degradation was separated into two parts: adsorption of CuNiN@C and activation of PMS. CuNiN@C adsorption followed a pseudo-second order rate model (R 2 = 0.99), and nitrogen doping caused multiple electron-withdrawing functional groups in order to achieve chemisorption. Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and N 2 adsorption of both the pre-test and post-test CuNiN@C were adopted in the adsorption mechanism investigation. Meanwhile, as the activate sites of CuNiN@C, Cu and Ni responded to the PMS activation, and three radicals may be generated during the activation. Radical quenching experiments and Electron Paramagnetic Resonance (EPR) illustrated that the hydroxyl radical ( OH) plays a major role in NFX oxidation, which was confirmed by the effect of pH value experiment. According to results of the liquid chromatograph linked to a mass spectrometer (LC-MS), possible degradation pathways are proposed: the substitution reactions and elimination reactions on both quinolone and benzene rings, the destruction of the piperazinyl group and the opening of the quinolone ring. This study provides new insight into the fabrication and application of the CuNiN@C/PMS system as antibiotic pollution remedy in aquatic environment.
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高影响因子
COMPOSITES PART B-ENGINEERING
·
2019
·
IF 6.864
Shanshan Xiao,Hui Mei,Daoyang Han,Laifei Cheng
SiC nw /C/Si 3 N 4 porous ceramic composites with layer-by-layer structure were successfully fabricated by freeze drying, carbonization and chemical vapor infiltration processes for excellent room and high temperature electromagnetic (EM) wave absorption properties . The sandwich-like structure within the layer and the capacitor model structure between the layers are formed inside of the composite, and these structures are beneficial to the EM wave consumption. The EM absorption properties are optimized by regulating the relative contribution of the polarization loss (primarily provide by SiC nw and defects in carbon phase) and the conductance loss (primarily offered by the conductive network formed by the carbon thin film). As an antioxidant protective layer, Si 3 N 4 ceramic coating is prepared on the outside of the carbon film . The prepared SiC nw /C/Si 3 N 4 porous composites show high absorption efficiency (exceed −39.7 dB), wide absorption band (cover the whole X band), small density (0.92 g/cm 3 ), thin thickness (2.9 mm), and excellent high-temperature stability (stable up to 873 K). The unique structures not only facilitate EM wave absorption, but also enable the composite a compressive strength of 168 MPa.
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CARBON
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2019
·
IF 7.466
Jinzhu Tang,Shuqing Chen,Yulong Jia,Ying Ma,Hongmei Xie,Xin Quan,Qi Ding
As a new type of carbon material, carbon dots (CDs) with exceptional properties are regarded as a type of potential water-based lubricant additive . In this study, it is first demonstrated that CDs perform excellently when used as lubricant additives for water-lubricated amorphous carbon (a-C) contacts. The results show that the introduction of CDs into water at a concentration of 0.1 wt% could reduce friction and wear in a-C contacts by 33% and 80%, respectively. Additionally, the lubricating performance of CDs is highly sensitive to its adding concentration. The excellent tribological performance of CDs results from the minimized CDs sediment particles (deposited in situ on worn a-C surfaces) and the reduced friction and wear via nano-bearing and nano-filling mechanisms. With high CDs concentrations, however, micron and submicron-sized sediment particles form when friction occurs and cause undesirable abrasive wear . For water-lubricated a-C contacts, therefore, the CDs concentration is the crucial determinant of lubrication performance that has to be appropriately controlled.
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高影响因子
International Journal of Applied Ceramic Technology
·
2022
·Vol. 20
·期 1
·527-533
·
IF 2.328
Mengwen Zhang,Lutong Yang,Zhaosheng Li,Binyang Jiang
Al 2 O 3 –cBN has received considerable attention in the field of ceramic cutting tools due to its high hardness, high wear resistance, and low cost, but poor interfacial bonding affects the performance of the composite. In this study, a novel hot-forging process was used to prepare high-performance Al 2 O 3 –cBN composites using Ti(C,N) as a binder. The evolution of the morphology, phase, and microstructure of the hot-forged Al 2 O 3 –Ti(C,N)–cBN composites was determined, and the mechanical properties were measured. The relative density of the composites increases significantly after hot forging, and the deformation of the composites increases with the hot-forging temperature. The highest performing Al 2 O 3 –Ti(C,N)–cBN composite was prepared by hot forging at 1600°C and has a hardness of 20 GPa, a bending strength of 647 MPa and a fracture toughness of 5.37 MPa m 1/2 , which are superior to those of a directly hot-pressed sintered composite. However, at hot-forging temperatures higher than 1700°C, Al 5 O 6 N and TiB 2 are formed in the composite. In the composite hot forged at 1800°C, serrated grain boundaries promote the strength and toughness of the composite to 877 MPa and 6.76 MPa m 1/2 , respectively. Therefore, the novel hot-forging process is expected to enhance material properties.
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高影响因子
INORGANIC CHEMISTRY
·
2022
·
IF 5.436
Zhen Pu,Jianwei Qin,Xiaoguo Fu,Ruizhi Qiu,Bin Su,Maobing Shuai,Fang Li
Fundamental investigation of metal–CO interactions is of great importance for the development of high-performance catalysts to CO activation. Herein, a series of side-on bonded mononuclear lanthanide (Ln) oxocarbonyl complexes OLn(η2-CO) (Ln = La, Ce, Pr, and Nd) have been prepared and identified in solid argon matrices. The complexes exhibit uncommonly low C–O stretching bands near 1630 cm–1, indicating remarkable C–O bond activation in these Ln analogues. The η2-CO ligand in OLn(η2-CO) can be claimed as an anion on the basis of the experimental observations and quantum chemistry investigations, although the CO anion is commonly considered to be unstable with electron auto-detachment. The CO activation in OLn(η2-CO) is attributed to the photoinduced intramolecular charge transfer from LnO to CO rather than the generally accepted metal → CO π back-donation, which conforms to the traditional Dewar–Chatt–Duncanson motif. Energy decomposition analysis combined with natural orbitals for chemical valence calculations demonstrates that the bonding between LnO and η2-CO arises from the combination of dominant ionic forces (>76%) and normal Lewis “acid–base” interactions. The fundamental findings provide guidelines for the catalyst design of CO activation.
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高影响因子
Journal of Environmental Chemical Engineering
·
2022
·
IF 7.968
Haoyang Wu,Zhilong Tan,Bin Miao,Hailong Hu,Sanying Hou
In this work, Fe, N co-doped hierarchical porous graphite-like carbon with carbon-encapsulated Fe/Fe 3 C@ Fe-N-C was synthesized by a facile solid-phase synthesis strategy, and was employed as an efficient catalyst to activate peroxymonosulfate (PMS) for oxidation of tetracycline (TC). The optimal Fe-N/C 800 outlined a highly catalytic performance in activating peroxymonosulfate (PMS) with TC decomposition rate reaching 89.2 % in 20 min at ultra-low catalyst dosage. Meanwhile, the effect of operating parameters was also investigated in order to evaluate the potential of using Fe-N/C 800 in practical applications. In addition, the characterization analysis and experiments results elucidated that graphitic N, pyridinic N, C O, Fe 3 C, Fe 0 and FeN 4 were considered as the main reactive species promoting the PMS activation to generate reactive oxygen species (ROS) (including singlet oxygen ( 1 O 2 ), sulfate radical (SO 4 •- ) and hydroxyl radical (•OH)). The electron paramagnetic resonance (EPR) experiments and radicals quenching analyses further demonstrated that the non-radical species singlet oxygen ( 1 O 2 ) was the dominant reactive oxygen species. Moreover, the TC degradation pathways were presented by LC-MS. Ultimately, the toxicity of the intermediate products were also investigated by ECOSAR system.
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APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Guohong Wang,Jianxi Liu,Xiangcheng Liu,Minghang Li,Jiongjie Liu,Nan Chai,Fang Ye,Jimei Xue,Xiaomeng Fan,Hailong Xu,Xingmin Liu,Laifei Cheng
MXenes have been the spotlight of interest as electromagnetic (EM) functional materials. However, the susceptibility (e.g., easy oxidation and fast decomposition) of MXenes leads to the fast fading of EM interference shielding effectiveness (EMI SE), which can be attributed to the easy degredation of MXene by reaction with water and oxygen in air. In this work, a series ofoxidation-resistant vitamin C/Ti 3 C 2 T X foam composites were developed as an EMI shielding material. The vitamin C/Ti 3 C 2 T X foam composites exhibited improved EM SE stability due to the protection of vitamin C by donating electrons. After exposing to air for 10 days, the EMI SE of vitamin C/Ti 3 C 2 T X foam decreased slightly from 42.5 dB to 41 dB while the EMI SE of Ti 3 C 2 T X foam dropped significantly from 47 dB to 35 dB. The EMI SE of vitamin C/Ti 3 C 2 T X foam and Ti 3 C 2 T X foam decreased correspondingly with further increase of exposuring time in air. However, the decreasing rate of vitamin C/Ti 3 C 2 T X foam is always slower than that of the Ti 3 C 2 T X foam. This work offers an effective way for the designing of oxidation-resistant MXene-based EMI shielding materials.
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高影响因子
DIAMOND AND RELATED MATERIALS
·
2023
·
IF 4.1
Yuanchun Zhang,Shengtao Gao,Jun He,Feng Wei,Xingzhao Zhang
Achieving a wide effective absorption bandwidth in 8.0–18.0 GHz under ultrathin thickness (d < 2.0 mm) with a low filler ratio is difficult. Herein, Co/Fe metal–organic framework (MOF)-derived CoFe@C composite-decorated residual carbon (CoFe@C/RC) hybrids collected from coal gasification fine slag (CGFS) by removing the inorganic oxide components were synthesized via a technology by modulating the molar ratio of Co/Fe. The physicochemical properties of the synthesized CoFe@C/RC with different molar ratios of Co/Fe were studied via various analytical techniques, and then the electromagnetic parameters associated with the above research results were analyzed. The defects, microstructure and electromagnetic wave absorption (EMWA) performance of CoFe@C/RC changed with the change in the Co/Fe molar ratio. Impressively, the Co 1 Fe 3 @C/RC hybrids exhibited excellent EMWA capacity . Under a filler content of 20 %, the ternary hybrid with a molar ratio of Co/Fe of 1:3 showed a minimum reflection loss ( RL min ) of −20.0 dB and a broad absorption bandwidth ( f e, RL ≤ −10 dB) of 3.95 GHz at a thickness of 1.7 mm. Importantly, the ultrabroad f e reached 10.0 GHz (8.0–18.0 GHz); it covered the whole Ku and X bands by simply adjusting the thicknesses of the CoFe@C/RC absorber in 1.5–3.0 mm. The CoFe@C/RC hybrids possessed outstanding EMWA because of the excellent effective synergy of magnetic and dielectric losses. This work realizes the high-value application of coal gasification solid waste and offers an efficacious strategy for creating novel CGFS residual carbon-based ultrathin EMW absorbing materials at 8–18 GHz.
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