MICROCHEMICAL JOURNAL
·
2020
·
IF 3.594
Xuejian Xing,Li Huang,Shaojing Zhao,Jiafu Xiao,Minhuan Lan
S,N-doped carbon dots (S,N-CDs) were facilely prepared via a hydrothermal method by using thiourea and citric acid (CA) as precursors. The as-prepared S,N-CDs exhibited high stability in aqueous solution and were applied for fluorometric detection of tetracyclines (TCs). The approach was developed on the basic of the fluorescence of S,N-CDs at 440 nm, which was selectively quenched by TCs through the inner filter effect (IFE) mechanism. Moreover, the fluorescence of TCs with maximum at 600 nm could be used as the internal standard signal, resulting in a fluorometric spectral response. The limit of detection (LOD) was 0.25, 0.39 and 0.26 μM for tetracycline (TC), doxycycline (DC) and oxytetracycline (OTC), respectively. Furthermore, S,N-CDs were successfully utilized for the detection of residual TCs in fish and pork samples with acceptable recovery and good RSD.
✓ 已验证
产品关联
DOI
高影响因子
MOLECULAR PHYSICS
·
2020
·
IF 1.767
Kaleem-Ur-Rahman Naveed,Li Wang,Haojie Yu,Raja Summe Ullah,Ahsan Nazir,Shah Fahad,Tarig Elshaarani,Muhammad Usman,Amin Khan
Understanding the segmental dynamics of polymer chains is cardinal to decipher the microscopic behaviour in order to modulate the bulk properties of polymers. The study of electron spin resonance (ESR) spectroscopy of spin-labelled polymers is useful to understand the segmental dynamics of polymer chains in solution. In this paper, poly(acrylic acid)s (PAAs) were spin labelled with 4-amino-2,2,6,6-tetramethylpiperidine-1-oxyl radicals. Spin-labelled PAAs (SL-PAAs) were characterised by Fourier-transform infrared spectroscopy, ultraviolet–visible spectroscopy, thermogravimetric analysis, differential scanning calorimetry, cyclic voltammetry (CV), and ESR analyses. The polyelectrolyte complexes of SL-PAAs were prepared by employing poly(diallyldimethylammonium chloride) (PDADMAC) as the polycation and analysed by transmission electron microscopy, dynamic light scattering (DLS), and ESR spectroscopies. The effect of molar mass on the segmental dynamics of SL-PAAs in pristine as well as in the form of polyelectrolyte complexes (PECs) was studied. The results indicated that SL-PAAs show a differential complexation behaviour with PDADMAC in the PECs depending on their molar mass.
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2021
·
IF 9.127
Ailing Tian,Kailin Luo,Zhendong Li,Mingming Ma,Shun Li,Xingyi Wang,Deyu Wang,Zhe Peng
Lithium (Li) metal and alloy anodes are strongly attractive for next high-energy-density batteries , owing to their high theoretical specific capacity and low redox potentials . However, the fast electrode pulverization caused by large volume variation upon cycling inhibits the use of the Li metal and alloy anodes seriously, whereas the sluggish charge transfer and weak electrode/electrolyte interphase are mainly responsible for their uneven volume expansion and surface breaks, respectively. Herein, a versatile F–N–S doped lithiophilic interphase is obtained via a one-pot electrochemical fabrication process with high controllability, which exhibits high robustness, Li affinity and fast Li transfer, and significantly outperforms the single lithiophilic interphase obtained via chemical route. When this advanced interphase is applied to the copper or aluminum electrodes, great stabilizations of Li plating/stripping or Li insertion/extraction processes can be achieved. This work emphasizes the importance of the interphase composition for designing stable high-energy-density electrodes, and gives insights on a general and efficient remedy to boost the performances of the large-volume-change electrodes.
✓ 已验证
产品关联
DOI
高影响因子
ACS Omega
·
2021
·
IF 3.512
Ze Yuan,Lanlan Yang,Dongni Han,Guorong Sun,Chenyu Zhu,Yao Wang,Qiao Wang,Mikhail Artemyev,Jianguo Tang
High-efficiency photoluminescence quaternary hexagon Zn–Cu–In–S (ZCIS) nanoplatelets (NPls) have been synthesized by a two-step cation exchange method, which starts with the In2S3 NPls followed by the addition of Cu and Zn. It is the first time that In2S3 NPls are used as templates to synthesize ZCIS NPls. In this paper, the reaction temperature of In2S3 is essential for the formation of NPls. The photoluminescence wavelength of NPls can be tuned by adjusting the temperature of Cu addition. To enhance the stability of the resulting NPls and to improve their optical properties, we introduced Zn2+ and obtained ZCIS NPls by cation exchange on the surface. It is worth noting that the obtained ZCIS NPls show a shorter fluorescence lifetime than other ternary copper sulfide-based NPls. This work provides a new way to synthesize high-efficiency, nontoxic, and no byproduct ZCIS NPls.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2021
·
IF 5.816
Jun Liu,Haorui Duan,Wenjie Xu,Jun Long,Wenheng Huang,Huan Luo,Jinchao Li,Yaping Zhang
A novel sulfonated multi-wall carbon nanotubes (s-MWCNTs) filler is synthesized by ring-opening reaction. And then, a series of branched sulfonated polyimide (bSPI)/s-MWCNTs composite membranes are also prepared for application in vanadium redox flow batteries (VRFBs). The optimized bSPI/s-MWCNTs-2% composite membrane has lower vanadium ion permeability (2.01 × 10 −7 cm 2 min −1 ) and higher proton selectivity (1.06 × 10 5 S min cm −3 ) compared to those of commercial Nafion 212 membrane. Moreover, the VRFB with bSPI/s-MWCNTs-2% composite membrane exhibits higher coulombic efficiencies ( CE s: 96.0–98.2%) and energy efficiencies ( EE s: 79.7–69.5%) than that with Nafion 212 membrane ( CE s: 86.5–92.5% and EE s: 78.5–67.6%) at 80–160 mA cm −2 . The VRFB with bSPI/s-MWCNTs-2% composite membrane has stable battery performance over 400 cycles at 100 mA cm −2 , whose EE value is in the top level among previously reported SPI-based composite membranes. The results show that the bSPI/s-MWCNTs-2% composite membrane has a great prospect in VRFB application.
✓ 已验证
产品关联
DOI
高影响因子
TRIBOLOGY INTERNATIONAL
·
2021
·
IF 4.872
Jian Wu,Yanlong Luo,Yifeng Chen,Xiaohua Lu,Xin Feng,Ningzhong Bao,Yijun Shi
Ionic liquids (ILs) are very potential lubricant additives for their strong adsorption and tribochemical reactions at the interface. In this work, poly(ionic liquid) of PImC 6 NTf 2 is used as lubricant additive in base oil of PEG, which can reduce the wear volume by around 65 times under 2.5 GPa. The lubricity is much more advantageous than the geminal dicationic IL of BIm 5 -(NTf 2 ) 2 . The adsorption strength of lubricants is studied by employing the microcalorimeter to evaluate the adsorption heat, AFM to test the adhesion force, and molecular dynamics simulation to calculate the interfacial binding energy. As a result, the adsorption strength of PImC 6 NTf 2 is obviously higher than BIm 5 -(NTf 2 ) 2 , and the lubricity is strongly dependent on the adsorption strength of ILs.
✓ 已验证
产品关联
DOI
高影响因子
EUROPEAN POLYMER JOURNAL
·
2021
·
IF 4.598
Zhaoquan Zheng,Bingyu Wang,Jing Chen,Yan Wang,Ziyue Miao,Cenyao Shang,Qiang Zhang
Glycopolymer has been developed in bactericidal applications, but the traditional synthesis, such as click chemistry, needs poly-step reactions and complicated processes. Herein, incorporating the glyco-units into the polymers by quaternization has been exploited to give a facile strategy by Copper-mediated reversible deactivation radical polymerization (Cu(0)-RDRP) to prepare quaternized poly(ionic liquid)s (PILs) with pendant saccharide. The obtained PILs have the suitable property of killing typical Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus . Simultaneously, they perform the lower hemolytic rate of blood cells, higher selectivity index against bacteria, and higher affinity with Concanavalin A (ConA) than those quaternized by bromohydrin at the same quaternization degree. This result demonstrated that the introduced saccharide units, such as glucose and mannose, could maintain the electrostatic interaction to kill bacteria, perform lectin recognition behavior and interaction with ConA, and relatively harmlessness against red blood cells. Moreover, the sugar-containing PILs became insoluble and still antibacterial after anion exchange reaction. These new findings illuminated that such quaternized antibacterial agents with saccharide units that are easy-to-prepare, low cytotoxic could pave the way for further water disinfectant and pathogen control application.
✓ 已验证
产品关联
DOI
高影响因子
RSC Advances
·
2021
·Vol. 11
·期 53
·33626-33636
·
IF 3.361
Leliang Wu,Yiting Lin,Yimin Zhang,Peng Wang,Mingjun Ding,Minghua Nie,Caixia Yan,Shiyao Chen
Alkaline substances could activate peroxymonosulfate (PMS) for the removal of organic pollutants, but relatively high alkali consumption is generally required, which can cause too high pH of the solution after the reaction and lead to secondary pollution. Within this study, PMS activated by a relatively low dosage of Ca(OH)2 (1 mM) exhibited excellent efficiency in the removal of bisphenol S (BPS). The pH of the solution declined to almost neutral (pH = 8.2) during the reaction period and conformed to the direct emission standards (pH = 6–9). In a typical case, BPS was completely degraded within 240 min and followed the kinetics of pseudo-first-order. The degradation efficiency of BPS depended on the operating parameters, such as the Ca(OH)2, PMS and BPS dosages, initial solution pH, reaction temperature, co-existing anions, humic acid (HA), and water matrices. Quenching experiments were performed to verify that singlet oxygen (1O2) and superoxide radicals (O2˙−) were the predominant ROS. Degradation of BPS has been significantly accelerated as the temperature increased. Furthermore, degradation of BPS could be maintained at a high level across a broad range of pH values (5.3–11.15). The SO4−, NO3− did not significantly impact the degradation of BPS, however, both HCO3− and HA inhibited oxidation of BPS by the Ca(OH)2/PMS system, and Cl− had a dual-edged sword effect on BPS degradation. In addition, based on the 4 identified intermediates, 3 pathways of BPS degradation were proposed. The degradation of BPS was lower in domestic wastewater compared to other naturals waters and ultrapure; nevertheless, up to 75.86%, 77.94% and 81.48% of BPS was degraded in domestic wastewater, Yaohu Lake water and Poyang Lake water, respectively. Finally, phenolic chemicals and antibiotics, including bisphenol A, norfloxacin, lomefloxacin hydrochloride, and sulfadiazine could also be efficiently removed via the Ca(OH)2/PMS system.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ELECTROCHIMICA ACTA
·
2019
·
IF 5.383
Jiaona Shi,Qi Kang,Yan Mi,Qingquan Xiao
Lithium-sulfur (Li–S) batteries have attracted extensive attention in the past decades owing to their high theoretical energy density, low-cost and eco-friendliness. However, poorly cycling stability and rapidly decay caused by shuttle effects at high-sulfur loading condition restrain their practical applications. Focusing on these issues, N-doped hollow porous carbon nanotubes (N-HPCNT) as a self-supporting sulfur cathode is developed. The inherent conductivity and abundant pores of 3D continuous framework not only allow a high-sulfur content (67 wt%) and block the polysulfides via physical confinement, but also trap the polysulfides by the nitrogen heteroatoms (4.60 wt%) via strong chemisorption . Benefiting from the above-mentioned merits, the self-supporting S/N-HPCNT cathode with 3 mg cm −2 sulfur delivers high reversible capacity, super rate capability (1152 and 852.8 mAh g −1 at 0.2 and 3 C, respectively) and long cycling stability (717.9 mAh g −1 after 500 cycles at 1 C). Even under a higher sulfur loading (8 mg cm −2 ), it still exhibits a stable areal capacity of 7.72 mAh cm −2 (corresponding to 965.1 mAh g −1 ) after 60 cycles. This work provides a pathway for developing high performance Li–S batteries.
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2019
·
IF 8.355
Shizong Wang,Jianlong Wang
High efficient and stable activator is desired for the sulfate radical-based wastewater treatment. Cobalt sulfide and cobalt oxide have high catalytic activity for peroxymonosulfate (PMS), but poor stability. Here, a novel composite, nano Co 9 S 8 and CoO encapsulated by nitrogen and sulfur co-doped sludge-derived biochar (CoO/Co 9 S 8 @N-S-BC) was synthesized, characterized and applied for activating PMS. The results showed that CoO/Co 9 S 8 @N-S-BC can effectively activate PMS for sulfamethoxazole (SMX) degradation, and 0.08 mM of SMX could be completely degraded within 10 min. The influencing factors, such as pH, temperature, chloridion, carbonate and humic acid were investigated. The SMX degradation conformed to pseudo first-order kinetics with rate constant of 0.379 min −1 . Sulfate radicals (dominant) and hydroxyl radicals contributed to SMX degradation. Carbon defects, pyridinic N, quaternary N, the carbon atoms next to pyridinic N, C O groups, -C-S-C and Co(II), all contributed to PMS activation.
✓ 已验证
产品关联
DOI
高影响因子
ADVANCED SYNTHESIS & CATALYSIS
·
2019
·Vol. 361
·期 13
·3191-3199
·
IF 5.451
Shuyun Ju,Mingxin Qian,Gang Xu,Lirong Yang,Jianping Wu
Optically pure 1,2,3,4-tetrahydroisoquinoline carboxylic acids constitute an important class of building blocks for the synthesis of natural products and synthetic pharmaceuticals. However, redox deracemization of racemic 1,2,3,4-tetrahydroisoquinoline carboxylic acids as an attractive method is still challenging for the lack of suitable oxidoreductases. Herein, a D-amino acid oxidase from Fusarium solani M-0718 ( Fs DAAO) with broad substrate scope and excellent enantioselectivity was exploited through genome mining, and applied for the kinetic resolution of a number of racemic 1- and 3-carboxyl substituted tetrahydroisoquinolines to yield the corresponding ( S )-enantiomers with excellent enantiomeric excess ( ee ) values (up to >99%). By using Fs DAAO in combination with ammonia-borane in one pot, deracemization of these racemic carboxyl-substituted tetrahydroisoquinolines was achieved with conversions up to >98% and >99% ee . Preparative-scale deracemization of racemic 1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid and 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid was also demonstrated with good isolated yields (82% and 73%, respectively) and ee >99%. Our study provides an effective method for the synthesis of enantiomeric pure 1,2,3,4-tetrahydroisoquinoline carboxylic acids. This method is expected to provide access to chiral carboxyl-substituted 1,2,3,4-tetrahydroquinolines and 1,2,3,4-tetrahydro-ß-carbolines.
✓ 已验证
产品关联
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2019
·
IF 3.45
Honghong Lei,Peng Jiang,Bin Li,Yuncheng Zhou,Rui Zhang,Jianlei Kuang,Wenbin Cao,Wei Wang
The (S, N) co-doped Ba 2 In 2- x Cr x O 5+ y (0 ≤ x ≤ 0.5) oxides are successfully obtained by mixing the Ba 2 In 2- x Cr x O 5+ y oxides and thiourea through a simple ball milling method followed by sintering at 400 °C for 3 h. The colors of the compounds change from orange-brown to yellow-green after reacting with thiourea. When Cr amount is small ( x = 0.1), the crystal structure of (S, N) co-doped Ba 2 In 2- x Cr x O 5+ y is orthorhombic Ba 2 In 2 O 5 phase. When x ≥ 0.3, the crystal structure of the sample is cubic BaInO 2.5 phase. And this phase transition is the same as Ba 2 In 2- x Cr x O 5+ y . XPS results reveal that Cr 6+ in Ba 2 In 2- x Cr x O 5+ y (0 ≤ x ≤ 0.5) oxides are reduced to Cr 3+ after sintering. S exists in both cation and anion forms, and N exists in substitutional forms. UV–Vis analysis indicates that the yellow-green hue comes from the d-d transition of Cr 3+ , and the doping of S, N ions leads to a red shift of the absorption edge of the samples.
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）