Skin collagen fiber-based radar absorbing materials

By using skin collagen fiber (CF) as raw material,Schiff base structure containing CF (Sa-CF) was synthesized through CF-salicylaldehyde reaction.Then a novel radar absorbing material (Fe-Sa-CF) was prepared by chelating reaction between Sa-CF and Fe 3+.The coaxial transmission and reflection method was used to analyze the complex permittivity and complex magnetic permeability of these CF-based materials,and the radar cross section (RCS) method was used to investigate their radar absorbing properties in the frequency range of 1.0-18.0 GHz.Experimental results indicated that the conductivity of CF increased from initial 1.08×10-11 to 2.86×10-6 S/cm after being transferred into Fe-Sa-CF,and its dielectric loss tangent (tanδ) in the frequency range of 1.0-17.0 GHz also increased.These facts suggest that the Fe-Sa-CF is electric-loss type radar absorbing material.In the frequency range of 3.0-18.0 GHz,Sa-CF (1.0 mm in thickness) exhibited somewhat radar absorbing property with maximum radar reflection loss (RL) of-4.73 dB.As for Fe-Sa-CF,the absorbing bandwidth was broadened,and the absorbing intensity significantly increased in the frequency range of 1.0-18.0 GHz where a maximum radar RL of-9.23 dB was observed.In addition,the radar absorbing intensity of Fe-Sa-CF can be further improved by increasing membrane thickness.When the thickness reached to 2.0 mm,the RL values of Fe-Sa-CF were-15.0-18.0 dB in the frequency range of 7.0-18.0 GHz.Consequently,a kind of novel radar absorbing material can be prepared by chemical modification of collagen fiber,which is characterized by thin thickness,low density,broad absorption bandwidth and high absorption intensity.     

考虑地质分层约束的长短期记忆循环神经网络测井曲线重构

延长油田东部裸眼井区早期测井资料普遍只有自然电位（SP）、自然伽马（GR）及梯度电阻率(R2.5)三条曲线,因缺失声波（AC）、地层电阻率（RT）等测井曲线,难以满足精细油藏地质研究需求。东部裸眼井区开发时间长、单井产量低,重新测井缺乏可行性及经济性。采用长短期记忆循环神经网络(Long Short-Term Memory,LSTM)进行缺失测井曲线重构是一种经济有效方法,适用于地层测井序列数据。然而延长油田东部浅层油藏上覆黄土层段测井数据信号干扰大,直接应用模型精度较差。针对此问题,本文采用考虑地质分层约束的LSTM模型进行缺失测井曲线的重构,通过分层数据截取每口井长6层段测井数据作为样本数据,既保留了LSTM模型处理序列数据的优势,同时又避免了上覆黄土层测井数据对模型的干扰。利用裸眼井区完整测井数据进行模型训练优化和验证,讨论了考虑地质分层约束的LSTM测井曲线重构精度,结果表明通过引入地质分层约束,模型重构测井曲线精度更高。应用优化后模型实现裸眼井区50口仅有GR、SP、R2.5三条曲线数据井的AC、RT曲线重构,对50口井的142个射孔段进行二次解释,对比试油解释结论符合率达到89.4%,验证了该方法对测井曲线重构的实用性和有效性。     

The determination of atmospheric phosphine in Ny-Ålesund

Phoshpine (PH3), a volatile and toxic gas, has been proved to commonly exist in the environment. The determination of gaseous phosphine and its emission fluxes in Ny-Ålesund is reported in this paper. Results showed that gaseous phosphine exist in Arctic atmosphere commonly and the concentration of phosphine ranged from 16.3–600.2 ng/m³, with the maximum concentration of phosphine in tundra areas and the minimum in surface air of ocean. The concentration of phosphine ranged from 65.79–1259 ng/m³ in colliery atmosphere at different altitudes and the maximum was found in the center of colliery. Emission fluxes of phosphine were different in various Arctic areas. Emission fluxes of phosphine from protected areas, with average concentration of 32.13±5.353 ng m^–2 h^–1, were higher than from other areas. And the flux of phosphine from ocean was lower.     

Research on catalysis of sodium-metallochlorophylls in Ni/MH battery

The effects of sodium-metallochlorophylls including sodium-iron chlorophyllin, sodium-copper chlorophyllin and sodium-magnesium chlorophyllin on performance of Ni/MH battery were investigated. The results show that sodium-iron chlorophyllin can effectively activate the gases produced during charge in Ni/MH battery, therefore reducing the reduction potential of oxygen and the oxidation potential of hydrogen, and the increased speed of inner pressure of battery is decreased significantly. With the aid of DMol3 software, the activation process of oxygen and hydrogen by sodiummetallochlorophylls was simulated and analyzed. It was found that the catalysis behavior is in agreement with the experimental results, and the activation process also gets a reasonable explanation from the calculated results.     

Hydroxyl radical electrochemically generated with water as the complete atom source and its environmental application

The most reactive hydroxyl radical （OH） was generated by electrochemical approach with safe water as the complete atom source. The direct evidence for OH formation was obtained by electron spin resonance method. The powerful OH electrochemically generated could effectively degrade organic pollutants and reduce the toxicity of wastewater. Electrochemical disinfection by OH was considerably efficient even without the aid of active chlorine. Bacteria inactivation of 99.99% was achieved for contact time of 30 min and current density of 5 mA·cm^-2, In comparison with active chlorine, OH is rather attractive as a promising environmentally benign disinfectant and opens a new route for microbial inactivation.     

An improved traitor tracing scheme based on bilinear map

T6 et al presented a bilinear-map-based traitor tracing scheme（TSZ scheme） with revocation, but it is a symmetric scheme because it does not provide non-repudiation. In this paper, an improved TSZ scheme was proposed by using oblivious polynomial evaluation （OPE） protocol and service parameters. Under the recondition of general sameness capabilities of both TSZ and improved TSZ scheme, the new scheme adds some advantages such as providing multi-service capability, user＇s non-repudiation and data provider＇s no-framing innocent users. Furthermore, it is also proved to be semantically secure under the decisional bilinear Diffie-Hellman （DBDH problem） assumption.     

New crystal structure of molecular complex 1-piperidine carboxylate-piperidinium-H<Subscript>2</Subscript>O studied by X-ray single crystal diffraction

Piperidine absorbs CO2 and H2O in air to form a molecular complex： piperidium-l-piperidinecarboxylate-H2O. The structure of the complex was characterized by X-ray single crystal diffraction. The crystal structure was determined to be triclinic, space group P1^-with a=0.648 6（8） nm, b=0.809 200） nm, c= 1.357 1（16） nm, a=96.96706）°, β =102.506（15）°,γ=104.202 05）°, Z=2. The complex is stabilized via five hydrogen bonds between the three components, N-O electrostatic interaction and O-O interaction （electron transfer） betweenl-piperidinecarboxylate and H2O. Due to electron transference of carbamate ion, the oxygen atom in water molecule is strongly negatively charged and the O-H bond is considerably shorter than that of the free molecule of water. The formation of the molecular complex is a reversible process and will decompose upon heating. The mechanism of formation and stabilization is further investigated herein.     

Erratum to: <Emphasis Type="Italic">In vitro</Emphasis> induction of mouse meningeal-derived iPS cells into neural-like cells

The authors report that incorrect figures were included as Figures 4 and 5 in the original publication of this paper. This error occurred during the figure editing process of the publishing company. This information should have been presented as follows:     

Serine/threonine protein phosphatases in DNA damage response

DNA damage response (DDR) is among the most important of the mechanisms that maintain genome stability which, when destabilized, predisposes organs to cancer. Reversible phosphorylation mediated by protein kinases and protein phosphatases regulates most, if not all, cellular activities, including DDR. Protein kinase inhibitors have become the main focus of targeted therapy and anticancer drug development. However, our limited knowledge of protein phosphatase function is compromising our capacity to develop therapeutic agents against phosphatases. In this review, we summarize the roles of serine/threonine protein phosphatases involved in DDR and propose that in situ dephosphorylation of phosphoproteins by protein phosphatases, instead of proteasome-mediated degradation of phosphoproteins, is mainly employed by cells.