JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2019
·Vol. 166
·期 2
·B49
·
IF 3.12
Di Liu,Fangxin Hu,Han Zhang,Cong Zhang,Shihong Chen
A sandwich electrochemiluminescence (ECL) biosensing system for soybean agglutinin (SBA) detection was developed with AuPt@C60 nanoflowers (AuPt@C60 NFs) as a novel co-reactant accelerator to enhance the performance of N-(aminobutyl)-N-(ethylisoluminol) (ABEI). In this strategy, nanoflower-liked AuPt@C60 complex served as a matrix for loading a large sum of ABEI and galactosamine (Gal) by Au-N and Pt-N bonds to achieve the nanocomposite Gal-ABEI-AuPt@C60 NFs. Dissolved oxygen was used as a co-reaction reagent, while AuPt@C60 complex acted as a co-reactant accelerator for dissolved oxygen to enhanced the ECL emission of ABEI. Gal, as an identifying element, was highly loaded by electrodeposited gold nanoparticles (Dp Au) on the electrode to recognize SBA, and further combine with Gal-ABEI-AuPt@C60 NFs to form a sandwich model. As a result, the proposed SBA biosensor exhibited a wide linear range from 1.0 ng·mL−1 to 5.0 μg·mL−1 and a low detection limit of 0.33 ng·mL−1. In addition, the biosensor displayed an excellent selectivity and an acceptable stability and reproducibility. The combination of AuPt@C60 NFs and ABEI provided a new ECL sensing platform without exogenous co-reactant.
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2021
·
IF 13.273
Jingwei Zhu,Yu Liu,Benlin He,Wenyu Zhang,Lifang Cui,Sudong Wang,Haiyan Chen,Yanyan Duan,Qunwei Tang
The back interface issues including numerous defects and imperfect contact, mismatched energy level are regarded as the key detrimental factors causing serious charge recombination and energy loss ( E loss ) and inferior charge extraction to achieve high efficiency Hole transport materials-free (HTMs-free) carbon-based Perovskite solar cells (PSCs). To address this drawback, an effective interface engineering via depositing N, N'-Dicyclohexylcarbodiimide (DCC) at PVSK/Carbon back interface is creatively implemented to passivate CsPbBr 3 surface defects through forming interaction between N atoms with lone pair electrons and uncoordinated ions (eg Pb 2+ and Cs + ions) to suppress the defect states induced non-radiative recombination and E loss . Concurrently, the smoothness and valence band of PVSK film with DCC modification are increased to improve the contact and band alignment at back interface, respectively, remarkably accelerating hole extraction and transportation and also reducing E loss as well as charge recombination. As a result, the comprehensive performance of DCC interface modified HTMs-free carbon-based CsPbBr 3 PSCs is significantly enhanced, especially the champion efficiency boosts to 10.16% from 6.60% of the control PSC. Furthermore, owing to the enhanced hydrophobicity and decreased imperfections of PVSK film with DCC modification, the optimized device without any encapsulation displays an excellent long-term stability under 85% RH air condition at 85 °C over 1200 h.
✓ 已验证
DOI
高影响因子
ANALYTICAL AND BIOANALYTICAL CHEMISTRY
·
2022
·Vol. 414
·期 20
·6047-6054
·
IF 4.478
Ma Qian,Qiao Juan,Liu Yufei,Qi Li
Recently, polymer-protected gold nanoparticles (AuNPs) have attracted extensive attention due to their good catalytic activities. However, how to regulate their catalytic activities by changing the polymer chain morphologies or the interactions between the ligands and the analytes through external stimuli is still a great challenge. This study describes a simple synthesis of AuNPs capped by thermo-responsive poly( N,N -dimethylacrylamide) (PDMAM). In comparison with three kinds of PDMAMs@AuNPs, PDMAM-2@AuNPs exhibited better peroxidase-mimic ability via the catalytic oxidation of 3,3’,5,5’-tetramethylbenzidine (TMB) with hydrogen peroxide (H 2 O 2 ) to generate oxidized TMB (oxTMB). Interestingly, its catalytic activity could be regulated by changing environmental temperature. Importantly, the addition of the antibiotic lomefloxacin endowed the PDMAM-2@AuNPs with enhancement in catalytic efficiency due to electrostatic interactions and the increased levels of reactive oxygen species. Based on this principle, a protocol for highly selective and sensitive monitoring of lomefloxacin has been constructed with the color change from pale blue to deep blue. The ultraviolet–visible absorbance of oxTMB at the wavelength of 650 nm showed a good linear relationship with antibiotic concentration in the range of 0.25–10.0 µM ( R 2 = 0.990). The limit of detection was 0.1 µM. The practical application of the proposed protocol with the promoted peroxidase-mimic activity for the measurement of lomefloxacin in capsules was realized. Graphical abstract
✓ 已验证
DOI
PubMed
高影响因子
International Journal of Environmental Research and Public Health
·
2016
·Vol. 13
·期 9
·925
·
IF 2.035
Hong-Qin Sun,Yang Du,Zi-Yang Zhang,Wen-Jing Jiang,Yan-Min Guo,Xi-Wu Lu,Yi-Min Zhang,Li-Wei Sun
Benzophenone (BP) andN,N-diethyl-3-methylbenzamide (DEET) are two chemicals often used in personal care products (PCPs). There is a lack of systematic ecotoxicological evaluations about the two chemicals to aquatic organisms. In the present study, the acute toxic effects onChlorella vulgaris,Daphnia Magana, andBrachydanio reriowere tested and the ecotoxicological risks were evaluated. For BP, the 96-h half-maximal effective concentration (EC50) onC. vulgariswas 6.86 mg/L; the 24-h median lethal concentration (LC50) onD. maganawas 7.63 mg/L; the 96-h LC50onB. reriowas 14.73 mg/L. For DEET, those were 270.72 mg/L, 40.74 mg/L, and 109.67 mg/L, respectively. The mixture toxicity of BP and DEET, onC. vulgaris,D. magana, andB. rerioall showed an additive effect. The induced predicted no-effect concentrations (PNECs) for BP and DEET by assessment factor (AF) method are 0.003 mg/L and 0.407 mg/L, respectively. Both are lower than the concentrations detected from environment at present, verifying that BP and DEET are low-risk chemicals to the environment.
✓ 已验证
DOI
高影响因子
MEDICINAL CHEMISTRY RESEARCH
·
2019
·Vol. 28
·期 9
·1388-1401
·
IF 1.72
Chen Xin,Liu Xiujie,Qiu kai,Xu Xiang,Li Caiwen,Wang Yan
According to the bio-isosterism theory, a series of N , N ’-disubstitutedphenyl-4-ethoxylbenzene-1, 3-disulfonamides ( 5a - p ) were designed and synthesized by two steps of reactions including chlorosulfonation and ammonolysis. The structures of all compounds have been confirmed by IR, 1 H-NMR, 13 C-NMR, and ESI-MS spectra. The in vitro anti-platelet aggregation activities were evaluated by Born’s test induced by adenosine diphosphate (ADP) and arachidonic acid (AA), respectively. The biological evaluation results revealed that compound 5h had the lowest IC 50 value (0.32 μM) and the highest inhibition rate (40.9 %) that of three positive control agents clopidogrel (0.41 μM, 23.5 %), aspirin (0.53 μM, 28.9 %), and picotamide (0.76 μM, 32.7 %). Afterwards, compounds with higher activities were selected to further study in vitro cytotoxicity via cell counting kit-8 (CCK-8) assay. The cytotoxicity results indicated that compound 5h had simultaneously the lowest cytotoxicity, while other compounds had no significant relationship between the anti-platelet activities and cytotoxicities. Based on above in vitro anti-platelet activity data, the SAR (Structure Activity Relationship) of the target compounds was preliminarily summarized. In general, N , N ’-disubstitutedphenyl-4-ethoxylbenzene-1, 3-disulfonamides have the potential of further study and very likely become safer and more effective anti-platelet agents.
✓ 已验证
DOI
高影响因子
JOURNAL OF ORGANIC CHEMISTRY
·
2024
·
IF 3.3
Jin Yan,Suijie Zhong,Xu Chen,Yihuan Luo,Hua Cao,Xiang Liu,Limin Zhao
Here, we report controlled and site-selective C–H alkenylation and dialkenylation of indolizines and pyrrolo[1,2-a]quinolines with β-alkoxyvinyl trifluoromethylketones under simple and practical conditions. Moreover, this direct C–H alkenylation strategy can also be extended to imidazo[1,2-a]pyridines. Notably, without a transition metal and external oxidant, efficient dehydrogenative β-alkenylation of tertiary amines with β-alkoxyvinyl trifluoromethylketones is presented.
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING RESEARCH & DESIGN
·
2018
·
IF 2.795
Mengjie Sun,Meng Li,Pin Wang,Xu Zhang,Cuiming Wu,Yonghui Wu
Anion exchange membranes are prepared by phase inversion of P84 co -polyimide to obtain porous structure, and then chemically modified by branched polyethylenimine. The porous membranes are compared with a dense P84 membrane. The dense membrane is hydrophobic with large area resistance (>85 Ω cm 2 ), while the porous membranes are hydrophilic with low area resistance (2.4–3.5 Ω cm 2 ), lower than that of commercial membrane CJMA-3 (6.0 Ω cm 2 ). The ion exchange capacities are in the range of 0.83–0.86 mmol/g and the water uptake values are 90–130%, both of which are higher than those of dense P84 membrane and CJMA-3 membrane (0.5–0.6 mmol/g; 15–20%). The P84 co -polyimide membranes are utilized in bipolar membrane electrodialysis (BMED) process to produce N -2-hydroxyethylpiperazine- N ′-2-ethanesulfonic acid (HEPES). The porous membranes can decrease the transport resistance of HEPES − ions and yield high recovery ratio and current efficiency, while the dense membrane is unsuitable for BMED . The output of HEPES is increased significantly if the membranes have finger- or tear-like pores, as well as higher ion exchange capacity. The HEPES − recovery ratios are 52.3–61.6% after running 6 h under 40 V, which are higher than that of membrane CJMA-3 (46.5%). The current efficiency can reach up to 86.1% and the energy consumption is only 3.92 kWh/kg by using the optimal porous membrane M-1, which are better than membrane CJMA-3 (65.5%, 5.15 kWh/kg). Hence, the porous membranes have high potential for producing organic acid with high molecular weight.
✓ 已验证
DOI
高影响因子
JOURNAL OF CHEMICAL THERMODYNAMICS
·
2020
·
IF 2.888
Taotao Zhan,Yuqi Su,Ying Zhang,Xiangyang Liu,Maogang He
The mutual diffusion coefficients of ethanol + n-heptane and diethyl carbonate (DEC) + n-heptane binary solutions were measured over the mass fraction from 0.05 to 0.95 at the pressure of 0.101 MPa, and at temperatures T = 288.15 K, 298.15 K, 308.15 K and 318.15 K. The expanded relative uncertainty ( k = 2) of the Mach-Zehnder digital holographic interferometry employed in the measurements was estimated to be less than 2.4% with the confidence level of 0.95. A semi-empirical correlation was used to fit the mutual diffusion coefficients as a function of concentration and temperature, which represents the experimental values with the absolute average relative deviations being 0.94% for ethanol + n-heptane and 0.90% for DEC + n-heptane. The temperature and concentration dependences of the mutual diffusion coefficients were investigated. The strongest non-ideal thermodynamic behaviors appear when the mass fraction of ethanol is within the limits of 0.45 to 0.65 or that of DEC is within the limits of 0.45 to 0.65. Besides, the mutual diffusion coefficients of ethanol + n-heptane and DEC + n-heptane binary solutions are found to be extremely sensitive to the solute concentration over the mass fraction of ethanol and DEC from 0.00 to 0.05, respectively.
✓ 已验证
DOI
高影响因子
POLYMER SCIENCE SERIES A
·
2018
·Vol. 60
·期 5
·612-617
·
IF 0.729
Wang Jinjing,Wang Huifeng,Li Yan,Tian Li,Chen Shanmin,Liu Qiang,Guo Zhen
A novel copolymer surfactant has been prepared via a free radical copolymerization of CO 2 -switchable monomer N , N -diethylaminoethyl methacrylate and the hydrophilic monomer sodium vinyl-sulfonate and characterized. The results of conductivity, dynamic light scattering and cryogenic transmission electron microscopy study showed the change of the microstructure of copolymer in water by adding or removing of CO 2 . The copolymer aqueous solution was found to exhibit reversible switchability by the bubbling of CO 2 /N 2 .
✓ 已验证
DOI
高影响因子
IEEE ELECTRON DEVICE LETTERS
·
2023
·Vol. 44
·期 7
·1152-1155
·
IF 4.9
Weishuai Duan,Zhe Liu,Xinfa Zhu,Biao He,Chao Fan,Yonghui Zhang,Mengjun Wang,Hongxing Zheng,Erping Li
Near-ultraviolet (NUV) detectors based on two-dimensional (2D) materials have garnered considerable attention owing to their atomic-scale thickness, varied bandgap, and strong interaction with incident light. In this work, homostructures composed of tin disulfide/chromium–doped tin disulfide (SnS
2
/Cr–SnS
2
) were proposed for 405 nm near-ultraviolet detectors. Afterward, superlative detectors were fabricated through the employment of micro-mechanical exfoliation and polydimethylsiloxane-assisted dry-transfer methods, anchored by the SnS
2
Cr–SnS
2
homostructures. The detectors demonstrated exceptional detection performance for 405 nm NUV radiation with a significant responsivity of
$2.04\times 10^{{3}}\,\,\text {A}\cdot \text {W}^{-{1}}$
and a short response time of 8 ms, exceeding that of detectors based on most 2D materials and even commercial light detectors (Thorlabs FD11A–Si). The work presents an effective homostructure for high-performance SnS
2
-based detectors, thereby opening an opportunity for the utilization of SnS
2
in NUV detectors.
✓ 已验证
DOI
高影响因子
DESALINATION
·
2025
·
IF 9.8
Minfu Mo,Yaling Lin,Danni Lin,Xiaojuan Ma,Yubin Hong,Lihui Chen,Dong Wang,Liulian Huang
Cellulose acetate (CA) has attracted much attention in the preparation of ultrafiltration membranes due to its green and sustainable characteristics. However, its poor performance (separation and antifouling performance, etc.) limits the application of CA-based membranes in water treatment. In this work, we prepared a cellulose acetate ultrafiltration membrane with enhanced separation performance by enhancing the dissolution process of CA. The dissolution process of CA was controlled by adjusting the ratio of mixed solvent ( N , N -dimethylacetamide (DMAC) and N -methyl pyrrolidone (NMP)), which could tune the phase conversion rate, optimizing the pore structures of the membranes. Compared to the single solvent (M0, M8), the optimal membrane (M4) exhibited a finger-like pore structure and the lowest surface roughness, which was favorable for achieving high water flux. As a result, the M4 possessed a comparable pure water flux (335.8 L·m −2 h −1 ) which was higher than M0 (1.8 times) and M8 (1.7 times), while the BSA rejection rate reached 96.4 %. Besides, the M4 showed a stable separation performance in different operation pressures, BSA concentration, and long-term experiments. This work provided a new method for the preparation of cellulose acetate ultrafiltration membrane with good separation performance and anti-fouling performance and also provides a new way for water treatment.
✓ 已验证
产品关联
DOI
高影响因子
Frontiers of Materials Science
·
2023
·Vol. 17
·期 3
·1-12
·
IF 2.7
Kang Min,Cheng Yizhu,Hu Yinchun,Ding Huixiu,Yang Hui,Wei Yan,Huang Di
Autonomous self-healing hydrogels were achieved through a dynamic combination of hydrogen bonding and ferric ion (Fe 3+ ) migration. N,N ′-methylenebis (acrylamide) (MBA), a cross-linking agent, was added in this study. Poly(acrylic acid) (PAA)/Fe 3+ and PAA–MBA/Fe 3+ hydrogels were prepared by introducing Fe 3+ into the PAA hydrogel network. The ionic bonds were formed between Fe 3+ ions and carboxyl groups. The microstructure, mechanical properties, and composition of hydrogels were characterized by field emission scanning electron microscopy and Fourier transform infrared spectroscopy. The experimental results showed that PAA/Fe 3+ and PAA–MBA/Fe 3+ hydrogels healed themselves without external stimuli. The PAA/Fe 3+ hydrogel exhibited good mechanical properties, i.e., the tensile strength of 50 kPa, the breaking elongation of 750%, and the self-healing efficiency of 82%. Meanwhile, the PAA–MBA/Fe 3+ hydrogel had a tensile strength of 120 kPa. These fabricated hydrogels are biocompatible, which may have promising applications in cartilage tissue engineering.
研究领域:
材料科学
·
生物医学工程
·
高分子科学
·
组织工程
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）