FOOD AND AGRICULTURAL IMMUNOLOGY
·
2019
·
IF 2.398
Xiangren Meng,Dejun Ji,Wei Zhang,Lixia Fu,Hengpeng Wang,Peng Wu
The nitrofurans were recently banned from use in livestock production due to their potential carcinogenicity in humans. Therefore, the screening of foods from animal origins for nitrofurans became mandatory. A rapid, specific and sensitive method based on immunochromatographic strip test has been developed for the determination of 3.5-dinitro-N’-(5-nitrofurfurylidene) salicylic acid hydrazide (DNSH) residues in fish. Fish samples were prepared by ultrasonic bath extraction, centrifugation, filtration, drying and res-suspension. The antigen (DNSH-glutaraldehyde-ovalbumin) and a goat anti-mouse IgG antibody were drawn onto a nitrocellulose membrane as the test and control line, respectively. Under optimal conditions, the DNSH cut-off limits for the test strips were determined as 10 ng/mL in 0.01 M phosphate buffered saline and 25 ng/mL in fish samples, with results obtained within 5min. Our data suggests this immunochromatographic assay can be used for the sensitive, rapid, and specific on-site screening of DNSH in fish products.
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RSC Advances
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2019
·Vol. 9
·期 21
·11676-11682
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IF 3.049
Yong Wei,Jijiang Fu,Hao Song,Ben Zhang,Chaoran Pi,Lu Xia,Xuming Zhang,Biao Gao,Yang Zheng,Paul K. Chu
Efficient and stable non-precious metal based electrocatalysts are crucial to the hydrogen evolution reaction (HER) in renewable energy conversion. Herein, CoxP nanoparticles (NPs) are uniformly embedded in N-doped TiO2 nanotube arrays (CoxP/N-TiO2 NTAs) by low-temperature phosphorization of the precursor of metallic cobalt NPs embedded in N-doped TiO2 NTAs (Co/N-TiO2 NTAs) which were fabricated by phase separation of CoTiO3 NTAs in ammonia. Owing to the abundant exposed surface active sites of CoxP NPs, tight contact between the CoxP NPs and TiO2 NTAs, fast electron transfer in N-doped TiO2, and channels for effective diffusion of ions and H2 bubbles in the tubular structure, the CoxP/N-TiO2 NTAs have excellent electrocatalytic activity in HER exemplified by a low overpotential of 180 mV at 10 mA cm−2 and small Tafel slope of 51 mV dec−1 in 0.5 M H2SO4. The catalyst also shows long-term cycling stability and is a promising non-precious metal catalyst for HER.
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IONICS
·
2019
·Vol. 25
·期 9
·4351-4360
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IF 2.289
Yu Zhongliang,Zhang Jiahe,Xing Chunxian,Hu Lei,Wang Lili,Ding Ming,Zhang Haitao
Boron-nitrogen co-doped graphene nanoarchitectures were synthesized by annealing a freeze-dried precursor containing exfoliated graphene oxide (GO) nanosheets, ammonium borate, and polyvinyl alcohol (PVA). The microstructures and composition of nanocomposites were optimized and characterized systemically. Effects of a doping element on the electrochemical performances and interface compatibility were evaluated. The restacking of exfoliated graphene nanosheets was hindered effectively by the ultra-fine carbon clusters formed via the thermal decomposition of PVA. Such a three-dimensional structure favors the fast mobility of electrolyte ions. In addition, the co-doping of N and B elements not only increases interface compatibility between ionic liquid electrolyte and graphene but also supplies extra pseudocapacitance. Benefiting from the integrated merits, the optimized nanocomposites could deliver a specific capacitance of 35.4 F g −1 at 1 A g −1 and present a maximum energy density of 78.7 Wh kg −1 with a power density of 2043 W kg −1 . Due to the formation of more decoupled ions in ionic liquid electrolyte at elevated temperature, the symmetric supercapacitors based on the as-formed nanocomposite exhibit a maximum energy density of 134.6 Wh kg −1 at 60 °C.
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IEEE SENSORS JOURNAL
·
2018
·Vol. 19
·期 5
·1633-1639
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IF 2.617
Ling Kong,Jie Chen,Zhiwei Chen,Jinhui Feng,Dawei Fan,Qin Wei
A new label-free aptasensor with high visible-light photoelectrochemical (PEC) activity was fabricated for the detection of AFB1 based on N-doped graphene quantum dots (N-GQDs) sensitized Zn-doped SnS2 (Zn-SnS2) nanocomposites. N-GQDs sensitized Zn-SnS2 showed an eminent PEC performance. Ascorbic acid was utilized as an efficient electron donor for scavenging photogenerated holes and inhibiting light driven electron-hole pair recombination. Under the optimum experimental conditions, the specific binding between AFB1 aptamer and AFB1 resulted in the linear decrease of photocurrent with the increase of logarithm of AFB1 concentration in the range of 0.01-20 ng mL-1 with a detection limit of 3 pg mL-1. The constructed N-GQDs sensitized Zn-SnS2 PEC aptasensor exhibited high sensitivity, low cost, and good reproducibility, which is a promising platform for the detection of other important analytes.
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Nature Communications
·
2019
·Vol. 10
·期 1
·1-9
·
IF 11.878
Qi Yu,Wang Jinyan,Kou Yan,Pang Hongchang,Zhang Shouhai,Li Nan,Liu Cheng,Weng Zhihuan,Jian Xigao
Aromatic N-heterocyclic compounds are very important chemicals, which are currently produced mostly from petroleum. Here we report that a pyridazine-based compound 6-(4-hydroxy-3-methoxyphenyl)pyridazin-3(2H)-one (GSPZ) can be efficiently synthesized by the Friedel-Crafts reaction of guaiacol and succinic anhydride, both of which can be derived from biomass. GSPZ is then treated with bio-based epichlorohydrin to prepare the epoxy resin precursor GSPZ-EP. With 4,4'-diaminodiphenylmethane as curing agent, GSPZ-EP possesses higher glass transition temperature (187 o C vs. 173 o C) and shows a 140%, 70 and 93% increase in char yield (in N 2 ), storage modulus (30 o C) and Young’s modulus, respectively when compared with a standard petroleum-based bisphenol A epoxy resin. Moreover, the cured GSPZ-EP shows good intrinsic flame retardancy properties and is very close to the V-0 rating of UL-94 test. This work opens the door for production of aromatic N-heterocyclic compounds, which can be derived from biomass and employed to construct high performance polymers.
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POLYMER BULLETIN
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2019
·Vol. 77
·期 2
·963-974
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IF 1.858
Yang Xu,Sun Zhaojie,Gao Jingru,Yang Chunhui,Tang Dongyan
Temperature-responsive films of poly( N -isopropylacrylamide) (PNIPAM) were facilely fabricated by one-step plasma-initiated polymerization and then functionalized by self-polymerization of dopamine on the surface. High retention of the monomer structure and temperature-responsive properties in PNIPAM films were confirmed. After plasma-initiated polymerization, PNIPAM films formed protrusions and ridges surfaces. Moreover, cross-linker of N , N ′-methylenebisacrylamide with different dosage was introduced into the systems to effectively modulate the roughness of PNIPAM films and to supply better adhesive surface. Furthermore, in cell culture, satisfactory survival rate of the attached Hela cells was obtained on PNIPAM films, and the cell viability was improved further on PNIPAM/PDA films. The results indicated that such films might be applicable in medical treatment and tissue engineering, due to their adjusted adhesion ability and less toxicity to cells.
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ANALYTICAL AND BIOANALYTICAL CHEMISTRY
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2019
·Vol. 411
·期 8
·1647-1657
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IF 3.286
Zuo Pengli,Liu Jianhua,Guo Hongna,Wang Chenghong,Liu Hongqian,Zhang Zhigang,Liu Qingyou
In this paper, we have presented a facile method to fabricate nitrogen and sulfur co-doped carbon dots (N,S-CDs) for blood methotrexate (MTX) sensing applications. The N,S-CDs with quantum yield up to 75% were obtained by one-step hydrothermal carbonization, using reduced glutathione and citric acid as the precursors. With this approach, the formation and the surface passivation of N,S-CDs were carried out simultaneously, resulting in intrinsic fluorescence emission. Owing to their pronounced temperature dependence of the fluorescence emission spectra, resultant N,S-CDs can work as versatile nanothermometry devices by taking advantage of the temperature sensitivity of their emission intensity. In addition, the obtained N,S-CDs facilitated high selectivity detection of Fe 3+ ions with a detection limit as low as 0.31 μM and a wide linear range from 3.33 to 99.90 μM. More importantly, the added MTX selectively led to the fluorescence quenching of the N,S-CDs. Such fluorescence responses were used for well quantifying MTX in the range of 2.93 to 117.40 μM, and the detection limit was down to 0.95 μM. Due to “inert” surface, the N,S-CDs well resisted the interferences from various biomolecules and exhibited excellent selectivity. The proposed sensing system was successfully used for the assay of MTX in human plasma. Due to simplicity, sensitivity, selectivity, and low cost, it exhibits great promise as a practical platform for MTX sensing in biological samples.
Graphical Abstract
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Scientific Reports
·
2018
·Vol. 8
·期 1
·1-11
·
IF 4.122
Zhuang Xueheng,Zhang Ying,Cai Chang,Zhang Jing,Zhu Yuejin
Magnetic microencapsulated phase change materials (magnetic MicroPCMs) are hotly researched for their dual-functions with phase change and magnetic properties, which provided the new applications in fields of maneuverable phase change materials and infrared electromagnetic dual shield. A series of magnetic MicroPCMs samples are synthesized by polymerization and coprecipitation method and the chemical composition contained poly(MMA-MAA) @ n-octadecane modified by Fe 3 O 4 . In addition, the characterizations exhibit the excellent magnetic and phase change properties. The magnetic MicroPCMs samples present 20 emu·g −1 saturation magnetization with still high enthalpy of 132 J·g −1 , which fully illustrates that the magnetic MicroPCMs fulfill both application on thermal energy storage and magnetic control.
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SYNTHESIS-STUTTGART
·
2019
·Vol. 51
·期 16
·3085-3090
·
IF 2.867
Menglan Wang,Yudong Li,Qing-An Wu,Shuping Luo,Yuehui Li
Indole scaffold synthesis relies primarily on oxidative C–H amination of N-protected alkenylanilines for C–N intramolecular cyclization reactions. Herein, for the first time, without N-protection, various readily prepared 2-alkenylanilines were transformed into the desired indole products in good yields by using K2S2O8 as oxidant in the presence of catalytic amounts of FeF2. The K2S2O8/FeF2 system offers a direct and benign synthetic route to 3-arylindoles and it is applicable to a wide range of substituted indoles including drug intermediates.
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Catalysis Science & Technology
·
2019
·Vol. 9
·期 9
·2282-2290
·
IF 5.726
Dawei Zhou,Peixue Wang,Yan Long,Yuqing Fei,Youquan Deng
The thermal cracking behavior of diethyl hexamethylenedicarbamate (EHDC) was investigated in this work. The polymers formed under different conditions were analyzed by IR and TG, indicating that the polymers were mixtures of EHDC, polyureas, imines and others. The polymers could be converted to EHDC by a simple alcoholysis reaction for the first time over Fe–Ni/Al2O3 catalysts. Under the optimized reaction conditions, the yield of EHDC could reach up to 52% with 99% selectivity over 8% Fe–3% Ni/Al2O3 catalysts. The catalysts were extensively characterized by BET, XPS, XRD, SEM, TEM, H2-TPR and NH3-TPD, showing that the interaction effect between Fe species and Ni species may be attributed to high catalytic performance of the catalyst. Meanwhile, the loss of active components resulted in decreased catalytic activity.
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2019
·
IF 4.175
Yuwei Ye,Yangjun Zou,Zilong Jiang,Qiumin Yang,Liyong Chen,Shengda Guo,Hao Chen
N doped carbon dots (N-CDs) were prepared by hydrothermal method in methacrylic acid and n -butylamine precursors. The inhibition behavior of N-CDs on Q235 steel in hydrochloric acid environment was discussed via weight loss test, surface characterizations and electrochemistry measurements. Results showed that the as-prepared N-CDs could effectively protect Q235 steel and the inhibition efficiency reached up to 94.96% at 200 mg/L of N-CDs. In the meantime, the impedance modulus was greatly enhanced and the corrosion current density was reduced by one order of magnitude after the addition of N-CDs. Moreover, it could adhere to the steel surface by diffusion and agglomeration effect, resulting in the formation of adsorption film on steel surface. The adsorption mechanism of N-CDs almost complied with the Langmuir adsorption model, containing chemical and physical adsorptions.
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Nanoscale
·
2019
·Vol. 11
·期 38
·17736-17745
·
IF 6.97
Qian Zhu,Fushan Wang,Fengwei Zhang,Zhengping Dong
The direct oxidation of alcohols to esters through a green and cost-effective strategy is a fascinating chemical synthesis route. In this study, an environmentally friendly N-doped porous carbon encapsulated Co-based nano-catalyst was prepared via a simple carbonization procedure, utilizing renewable chitosan, accessible dicyandiamide and low-cost Co(OAc)2 as co-precursors. The obtained Co@NC-2-T catalysts were successfully used in selective oxidation of aromatic alcohols with methanol to esters under atmospheric reaction conditions. The Co@NC-2-900 catalyst (added with 2 g dicyandiamide and pyrolyzed at 900 °C) shows optimal activity and applicability and can also be reused at least six times in the oxidative esterification of aromatic alcohols with excellent stability. The presence of superoxide anion radicals in the current catalytic system was detected by the EPR method, and a possible mechanism of alcohol oxidation to ester was proposed on this basis. Thus, this study provides a facile, eco-friendly, and highly efficient catalytic system for oxidative esterification of alcohols.
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