Journal of Inorganic and Organometallic Polymers and Materials
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2018
·Vol. 29
·期 1
·269-278
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IF 1.754
Sun Li,Li Haonan,Lv Pengcheng,Chen Jian
Gold nanoparticles (Au NPs) were rapidly synthesized in the Sargentgloryvine stem (Ss) extract without the addition of any chemical agent at room temperature. The synthesis time was less than 10 min (even 1.5 min). The reducing and capping properties of the Ss extract were systematically investigated and then the controllable synthesis of Au NPs was achieved based on UV–Vis spectra. Au NPs were further characterized by transmission electron microscopy, selected area electron diffraction, X-ray diffraction and energy-dispersive X-ray spectroscopy analyses. It could be found Au NPs were quasi-spherical with an average size of 15.6 nm and a face-centered cubic crystalline structure. As-obtained Au NPs was used as photocatalysts for the degradation of nitro compounds (2-, 3-, 4-nitrophenol and 2-nitroresorcinol) and exhibited remarkable photocatalytic activity and stability. The rate constants ( K ) of nitro compounds degradation followed the order: K 4-NP > K 2-NP > K 3-NP > K 2-NR . The difference of the rate constants could be caused by the substituent effect originated from different molecular structures of nitro compounds. The rate constant for the 4-nitrophenol degradation could be linearly adjusted by the molar concentration of Au NPs in the degradation system, which is favorable to the practical wastewater treatment. Graphical Abstract
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Journal of Applied Spectroscopy
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2018
·Vol. 85
·期 3
·437-444
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IF 0.611
Zhao Lingzhi,Zhao Liu,Zhang Chenxiao,Li Yanqi
We demonstrate the utility of 4-chloro-7-nitrobenzofurazan (NBD-Cl), a simple, low-cost probe, for colorimetrically and fluorescently detecting and differentiating similar thiol species, including cysteine, homocysteine, and glutathione, as well as for assaying acetylcholinesterase (AChE) activity. This assay is a potential tool for investigating thiol functions in disease and diagnosis, and for screening AChE inhibitors. We envision that this versatile probe, which is commercially available and inexpensive, will be useful for further elucidating the roles of thiols in biology and also shows applicability for analysis of AChE inhibitors in physiological samples.
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Nature Communications
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2018
·Vol. 9
·期 1
·1-8
·
IF 12.353
Pan Xiao-Feng,Gao Huai-Ling,Lu Yang,Wu Chun-Yan,Wu Ya-Dong,Wang Xiang-Ying,Pan Zhi-Qiang,Dong Liang,Song Yong-Hong,Cong Huai-Ping,Yu Shu-Hong
Biomimetic assembly of high-quality nanosheets into nacre-like structures can produce macroscopic films with favorable mechanical and optical performances due to the intrinsic properties and high level of ordering of the nanoscale building blocks. Natural ground mica is abundant and exhibits great application potential. However, large size and low aspect ratio greatly limit its biomimetic assembly. Moreover, exfoliation of ground mica into high-quality nanosheets remains a significant challenge. Here, we report that large-scale exfoliation of ground mica into mono- or few-layered mica nanosheets with a production rate of ~1.0 g h − 1 can be successfully achieved. The mica nanosheets are then assembled into strong biomimetic polymeric mica film that inherits the high electric insulation, excellent visible transmittance, and unique ultraviolet-shielding properties of natural mica. Its overall performance is superior to that of natural sheet mica and other biomimetic films, making the polymeric mica film a suitable substrate for flexible and transparent devices.
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MICROCHIMICA ACTA
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2018
·Vol. 185
·期 5
·1-8
·
IF 5.705
Sang Fuming,Liu Jia,Zhang Xue,Pan Jianxin
A colorimetric method is described for the determination of Pt(II). It is based on the use of gold nanoparticles (AuNPs) which are known to aggregate in the presence of a cationic polymer such as poly(diallyldimethylammonium chloride) (PDDA). If, however, a mismatched aptamer (AA) electrostatically binds to PDDA, aggregation is prevented. Upon the addition of Pt(II), it will bind to the aptamer and induce the formation of a hairpin structure. Hence, interaction between aptamer and PDDA is suppressed and PDDA will induce the aggregation of the AuNPs. This is accompanied by a color change from red to blue. The effect can be observed with bare eyes and quantified by colorimetry via measurement of the ratio of absorbances at 610 nm and 520 nm. Response is linear in the 0.24–2 μM Pt(II) concentration range, and the detection limit is 58 nM. The assay is completed within 15 min and selective for Pt(II) even in the presence of other metal ions. It was successfully applied to the rapid determination of Pt(II) in spiked soil samples.
Schematic representation of the method for detection of Pt(II) based on the use of a cationic polymer and gold nanoparticles. In the presence of Pt(II), aptamer interacts with the Pt(II) and prevents the interaction between aptamer and cationic polymer. Hence, cationic polymer induce the aggregation of the AuNPs and lead to the color change from red to blue.
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JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY
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2018
·Vol. 134
·期 3
·2041-2048
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IF 2.209
Wu Cheng-Jie,You Jin-Zong,Wang Xue-Jie
Piroxicam (PRX) is a nonsteroidal anti-inflammatory drug. The thermal decomposition process of PRX was investigated with thermogravimetry and differential scanning calorimetry. The gaseous products generated by thermal decomposition were characterized with thermogravimetric analysis coupled with Fourier transform infrared spectroscopy. The residues of the thermal decomposition at various temperatures were identified with infrared spectroscopy. The molecular bond orders were calculated using an ab initio method from the GAMESS program of quantum chemistry. The mechanism of thermal decomposition for PRX was discussed. The results indicated that the thermal decomposition of PRX is a two-stage process with the initial temperature of 198 °C either in nitrogen or air atmospheres. The thermal decompositions of the first stage in two atmospheres are the same process. The main part of the molecule, including sulfamide, amide, benzene ring and pyridine ring, decompose simultaneously and to form gasifiable small molecules and carbonaceous residue in the first stage. The second stage in nitrogen is a slow thermal pyrolysis process of carbonaceous residue. The forepart of the second stage in air is a slow thermal pyrolysis process as like as in nitrogen, and the later period of the second stage is an oxidation (combustion) reaction process of carbonaceous residue. PRX is stable under ambient temperature and air atmosphere, and it can be preserved for long-term storage under ambient temperature and in air atmosphere.
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International Journal of Intelligent Robotics and Applications
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2018
·Vol. 2
·期 4
·445-453
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IF 0
Liu Yanting,Liu Yang,Shen Yajing
The bottom-up organization of noble metal nanostructures with nanometer-scale precision is an important goal in nanotechnology. Owing to their unique localized surface plasmon resonance, well-defined metal nanostructures arrays could be used to develop applications in nano-photonics, nano-plasmonics, and nano-electronics. This article proposes an alternative pathway of a controllable approach to assemble and weld together the gold nanostructures. As a typical plasmonic nanostructure, the gold nanorods (Au NRs) was synthesized by the classical seed-mediated growth method. Based on the recognition of biomolecules through complementary DNA hybridization, we used DNA origami strategy for controllable assembly of Au NRs. Rectangular DNA origami as a template can induce the geometrically assembled of Au NRs. We designed and fabricated tip-to-tip Au NRs dimers on the DNA templates. Then,the follow-up formation of nanojunctions between assembled tip-to-tip Au NRs dimers Au NRs was conducted by irradiating infrared femtosecond pulses laser. The ability to coupling plasmonic nanostructures by assembly and nano-welding could be fundamental to developing novel optical properties and ensuring materials.
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JOURNAL OF MATERIALS SCIENCE
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2018
·Vol. 54
·期 5
·4115-4123
·
IF 2.993
Zhou Xiang,Zhu Ying,Ke Xiang,Zhang Kaili
In this study, we use simultaneous differential scanning calorimetry and thermogravimetric analysis to analyze the solid-state reaction characteristics of Al/Fe 2 O 3 nanothermites before n -Al melts. Different experimental setups for thermal analysis are compared, and the heat-release characteristics are studied on Al/Fe 2 O 3 nanothermites in the form of powder and pellet, respectively. It is found that protection provided by mere argon flow is far from enough for thermal analysis of Al/Fe 2 O 3 nanothermites. The experimental setup must be free of oxygen; otherwise, the determined exothermic peak is mostly the oxidation of n -Al by the residue oxygen molecules in the furnace body, due to the high reactivity and moderate accessibility of free oxygen molecules. Under proper experimental setup, it is found that besides the redox reaction between n -Al and n -Fe 2 O 3 , intermetallic reaction also occurs to form Fe 4 Al 13 . Moreover, the intermetallic reaction is more noticeable for nanothermite pellet than for nanothermite powder, and the eutectic reaction of Fe 4 Al 13 and n -Al leads to melting peaks below 655 °C. The results indicate that instrument configuration and sample status affect the testing results to a large extent, and one should be prudent to derive reaction characteristics of nanothermites.
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MICROCHIMICA ACTA
·
2018
·Vol. 185
·期 11
·1-10
·
IF 5.705
Zhu Xiang,Wang Jianying,Zhu Yuhua,Jiang Honghao,Tan Di,Xu Ziqiang,Mei Tao,Li Jinhua,Xue Longjian,Wang Xianbao
N,S-co-doped carbon dots (N,S-CDs) were synthesized via a single-step solvothermal process by using sodium lignosulfonate and p-phenylenediamine as carbon/nitrogen/sulfur sources. The N,S-CDs have an average diameter of 2.02 ± 1 nm and display green fluorescence, with excitation/emission peak wavelengths at 380/540 nm for optimal fluorescence. Fluorescence is excitation wavelength-dependent and stable in aqueous salt solutions. The fluorescence of the N,S-CDs is selectively quenched by Fe(III) and Ag(I) ions. These ions can be quantified by fluorometry with a limit of detection of 1.7 μM for Fe(III) ions and 11.6 μM for Ag(I) ions. The N,S-CDs also undergo solvatochromism in that emission is green in water solution but blue in polar organic solvents such as ethanol or N,N-dimethylformamide. The color of fluorescence gradually shifts from green to blue when continuously increasing the fraction of organic solvent in water.
N,S-co-doped carbon dots (N,S-CDs) are synthesized by using sodium lignosulfonate and p-phenylenediamine as C/N/S sources. The N,S-CDs can sensitively detect Fe(III) and Ag(I) ions based on fluorometry, and can be used as a solvatochromic probe.
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International Journal of Peptide Research and Therapeutics
·
2018
·Vol. 25
·期 4
·1319-1331
·
IF 1.132
Liu Huifan,Wu Hui,Wang Qin
In a previous study a crude peptide extract was obtained from Dendrobium aphyllum , and this study focused on the functional characterization of the peptide fraction (named DPP) after being purified by DEAE Sepharose. The DPP with high purity contained 16 types of free amino acids and 6 polypeptides. DPP could act as the AAPH-free radical scavenger to protect the erythrocyte under oxidative stress, and the attenuation significantly increased after intestinal digestion. Moreover, the results of the Caco-2 cell models indicated the high absorptive and transfer rates of DPP, in which the passive diffusion was the major transfer pathway. Through the LC-TOF/MS-MS analysis, the peptide sequences Asp-Asp-Asp-Tyr and Asp-Tyr-Asp-Asp were very sensitive to the gastric environment and were completely degraded by Caco-2 cells. While Ser-Ser-Arg, Ala-Val-Thr-Phe , and Met-Leu-Cys-Ala resisted the gastric condition; and sequence Met-Leu-Cys-Ala maintained its structure after the subsequent intestinal digestion and the Caco-2 cells’ uptake.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2018
·Vol. 29
·期 24
·20546-20553
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IF 2.324
Xin Miao,Zhang Liming,Chang Yi,Ren Luchao,Luo Xianfu,Zhou Hongqing
This present work aimed to attain a high-performance tape for LTCC application by using butyl benzyl phthalate as plasticizer in tape casting slurry of CaO–SiO 2 –B 2 O 3 glass–ceramics. The plasticizing mechanism of butyl benzyl phthalate in suspensions was demonstrated in depth. Dried droplets of binder were prepared to preliminarily judge the compatibility of binder and plasticizer, and the optimal additive amount was determined by rheological characteristic. In addition, a series of qualitative and quantitative methods were carried out to assess the tensile strength and elongation of green tapes, microwave properties and densification of sintered bodies. The experimental results revealed that when the addition of BBP was up to 45 wt%, tape casting slurries had the optimal fluidity and green tapes obtained the excellent performance with density at 1.65 g/cm 3 , tensile strength at 1.43 MPa and elongation at 13.4%. Meanwhile, sintered bodies fired at 850 °C achieved the highest density at 2.42 g/cm 3 with ε r = 5.94 and tanδ = 10 × 10 −4 at 10 GHz.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2018
·Vol. 29
·期 22
·19111-19122
·
IF 2.324
Duan Haojie,He Yue,Li Shouchun,Liu Li,Xu Suyang,Li Yu,Li Haiying,Gong Yimin,Liang Qingcheng,Cheng Yali
The pure and Tb-doped In 2 O 3 beaded-porous nanotubes (BPNTs) are fabricated by simple electrospinning method. The crystal phase, morphology and chemical composition of the obtained samples were analyzed by characteristic techniques (XRD, FE-SEM, TEM, EDS, XPS, etc.). The mechanism of forming BPNTs structure was studied, and phase separation plays a key role in the process of formation. A series of sensing tests toward formaldehyde gas showed that 6 mol% Tb-doped In 2 O 3 BPNTs exhibited the best sensing performance: high response (75–50 ppm), shorter response and recovery times (2 s and 12 s), low limit of detection (LOD, 1.27–100 ppb), good selectivity and long-term stability, etc. The significantly improved gas sensing properties were mainly resulted from their high surface basicity, enriched defects (oxygen vacancies), small crystallite size and complex porous structures.
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2018
·Vol. 25
·期 27
·27274-27282
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IF 2.8
Luo Jingyang,Zhang Qin,Wu Lijuan,Cao Jiashun,Feng Qian,Fang Fang,Chen Yinguang
1,4-Dioxane is an emerging pollutant, which widely exists in natural environments and poses potential risks to the living organisms. However, its effect on the denitrification process is still unknown. In this study, the effects of 1,4-dioxane on the denitrification process were therefore investigated by using Paracoccus denitrificans as the model denitrifier. The obtained results showed that the exposure of 1,4-dioxane exhibited remarkable lag or inhibition on the denitrification process, especially with high dose. In the control without 1,4-dioxane exposure, Paracoccus denitrificans showed high denitrification efficiency (98.5%). However, the efficiency decreased to 78.5, 63.9, and 9.3% with 0.50, 0.75, and 1.0% ( v / v ) 1,4-dioxane dose, respectively. The dose-induced inhibition of denitrification by 1,4-dioxane could be partially attributed to the negative effects on proliferation and viability of functional microorganisms by conjugating and disrupting the cell membranes. Furthermore, 1,4-dioxane caused biotoxicity to the intracellular activities of denitrifiers via disturbing carbon source utilization and interfering the key enzymes responsible for glycolysis. The decrease of microbial viability and activity inevitably resulted in the decline of key enzymes (NAR, NIR, NOR, and N 2 OR) closely related with denitrification process, which could be the direct reason for the decrease of denitrification performance.
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