Ceria-Co-Cu-based SOFC anode for direct utilisation of methane or ethanol as fuels

Nickel-free solid oxide fuel cell anodes are an object of study for applications that aim at utilising primary carbonaceous fuels to generate power. In this study, a ceria-Co-Cu anode is produced and tested with hydrogen, methane and ethanol fuels at various temperatures.The produced catalysts were characterised by X-ray analysis and H₂ temperature-programmed reduction (TPR). Catalytic tests were performed and compared with the material under electrochemical operation. The cells were electrochemically characterised by recording i-V plots. The samples were assessed post-test for eventual carbon deposits by Raman spectroscopy investigations and temperature-programmed oxidation (TPO) analysis.The cells were able to operate with hydrogen, methane as well as ethanol, directly fed to the anode, with maximum power densities ranging from 400 to 540 mW.cm⁻², depending on the fuel stream utilised. The cells also kept their integrity demonstrating coking resistance for over 24 h of continuous operation. Important discussions and conclusions are drawn about carbon formation and the role of each compound in the anode composition. The bimetallic cell (ceria-Co-Cu) is herein compared to monometallic ones (ceria-Co and ceria-Cu) that served as baselines. The advantages of the bimetallic composition are listed and evaluated throughout the discussions.     

废菌渣活性炭的制备及对废水中硝基苯的吸附

以废菌渣为原料制备活性炭，采用能量-色散光谱（EDS）和傅里叶变换红外光谱仪（FTIR）进行表征，结果表明：活性炭表面具有多种官能团，有利于提高对硝基苯的吸附。并研究了活性炭吸附硝基苯的影响因素（pH、初始浓度、吸附时间、投加量）、吸附等温线及热力学。结果表明：在常温中性pH条件下，初始浓度为50mg/L，活性炭用量为0.15g时硝基苯去除率可达98%，出水水质满足《污水综合排放标准》（GB 8978－1996）中对硝基苯浓度低于2.0mg/L的要求。活性炭对硝基苯的吸附具有较快的吸附速率，即1min接近平衡。该吸附行为是自发放热反应，可以用Freundlich模型很好地拟合。废菌渣活性炭对硝基苯的吸附主要是疏水作用和氧化钼活化共同作用的结果。因此，以农业废弃物-废菌渣制备得到的废菌渣活性炭具有良好的经济实用性，可用于废水处理中，实现以废治废的目的。     

适用于无线体域网的动态口令认证协议

无线体域网中传输的是与生命高度相关的敏感数据，身份认证是信息安全保护的第一道防线。现有的基于人体生物信息的身份认证方案存在信息难提取、偶然性大和误差性大的问题，基于传统密码学的认证方案需较大计算资源和能量消耗，并不适用于无线体域网环境。为此，在动态口令和非对称加密机制基础上，提出一种适用于无线体域网的动态口令双向认证轻量协议，并对其进行形式化分析。通过理论证明、SVO逻辑推理及SPIN模型检测得出：该协议满足双向认证，且能够抵御重放攻击、伪装攻击、拒绝服务器攻击和口令离线攻击，具有较高安全性。     

高速纺纱锭子弹性管减振机制与振动特性

为探究锭子弹性管的减振机制,将其开螺旋槽部分作为矩形弹簧模型处理,建立了减振弹性管的抗弯刚度及底部振幅的理论数学模型,并利用MatLab仿真分析了减振弹性管关键结构参教与其抗弯刚度和底部振动特性的耦合关系,同时结合有限元仿真及模态测试得到弹性管各阶固有频率。研究结果表明:随着槽宽和圈数的增大,刚度降低,底部振幅增加;随着壁厚、螺距、螺旋升角、弹性模量的增大,刚度增加,底部振幅降低;弹性管固有频率和锭子系统共振频率区间一致,且工作频率有效避开了共振频率。     

Biomass-derived carbon nanosheets coupled with MoO2/Mo2C electrocatalyst for hydrogen evolution reaction

Transition metal carbide such as molybdenum carbide has been widely used in electrolytic water for hydrogen production due to its potential catalytic property. The synthesis of molybdenum carbide-based high-efficient catalysts by simple process remains great challenges. Herein, Mo oxide/carbide material with hybrid morphology was synthesized by carbonizing mixture of lotus roots and Mo salt. The as-obtained material consists of MoO₂/Mo₂C (MOMC) anchored on biomass-derived nitrogen-doped carbon (NC) matrix. The results show that as-prepared material displays leaf-like and belt-like nanosheets, and the MOMC/NC catalyst with optimal Mo contents exhibits an excellent activity with a low overpotential of 138 mV to drive 10 mA cm^?2 and Tafel slope is 56.7 mV dec^?1 in alkaline medium, indicating that as-prepared catalyst will have promising application in the field of catalysis.     

Characterization of four diol dehydrogenases for enantioselective synthesis of chiral vicinal diols

Enantiopure vicinal diols are important building blocks used in the synthesis of fine chemicals and pharmaceutical compounds. Diol dehydrogenase (DDH) mediated stereoselective oxidation of racemic vicinal is an efficient way to prepare enantiopure vicinal diols. In this study, four new bacterial DDHs (AnDDH from Anoxybacillus sp. P3H1B, HcDDH from Hazenella coriacea, GzDDH from Geobacillus zalihae and LwDDH from Leptotrichia wadei) were mined from the GenBank database and expressed in E. coli T7. The four DDHs were purified and biochemically characterized for oxidation activity toward (R)-1-phenyl-1,2-ethanediol, with the optimal reaction condition of pH9.0 (AnDDH), 10.0 (HcDDH) and 11.0 (GzDDH and LwDDH) and the temperatures at 40℃ (AnDDH), 50℃ (HcDDH) and 60℃ (GzDDH and LwDDH), respectively. The four enzymes were stable at the pH from 7.0 to 9.0 and below 40℃. Kinetic parameters of four DDHs showed that the HcDDH from Hazenella coriacea had high activity toward a broad range of vicinal diols. A series of racemic vicinal diols were successfully resolved by recombinant E. coli (HcDDH-NOX) resting cells co-expression of an NADH oxidase (NOX), affording (S)-diols and (1S, 2S)-trans-diols in ≥ 99% ee. The synthetic potential of HcDDH was proved by E. coli (HcDDH-NOX) via kinetic resolution of racemic trans-1,2-indandiol on a 100 ml scale reaction, (S, S)-trans-1,2-indandiol was prepared in 46.7% yield and >99% ee. In addition, asymmetric reduction of four α-hydroxy ketones (10-300 mmol·L^-1) by E. coli (HcDDH-GDH) resting cells resulted in >99% ee and 69-98% yields of (R)-vicinal diols. The current research expands the toolbox of DDHs to synthesize chiral vicinal diols and demonstrated that the mined HcDDH is a potential enzyme in the synthesis of a broad range of chiral vicinal diols.     

Photoelectrocatalytic hydrogen production of heterogeneous photoelectrodes with different system configurations of CdSe nanoparticles,Au nanocrystals and TiO2 nanotube arrays

The different configurations of CdSe nanoparticles, Au nanocrystals and TiO₂ nanotube arrays play an important role in the photoelectrochemical behavior and photoelectrocatalytic hydrogen production of this heterogeneous photoelectrode system. It is discovered that the photoelectrocatalytic hydrogen production of the TiO₂–CdSe–Au photoelectrode (1.724 mmol g⁻¹ h⁻¹) is about 4 times that of the TiO₂–Au–CdSe photoelectrode (0.430 mmol g⁻¹ h⁻¹) under visible light irradiation. From the comprehensive investigation of their photoelectrochemical behaviors, it is illustrated that the interfacial electrical field has distinct effects on the separation and transportation of photogenerated carriers in these heterostructure photoelectrodes. The directions of the interfacial electrical fields formed at TiO₂–Au and Au–CdSe interfaces are opposite in the TiO₂–Au–CdSe photoelectrode, which hinders the separation of photogenerated electron-hole pairs and subsequent transportation of photogenerated carriers. On the contrary, the directions of the interfacial electrical fields formed at TiO₂–CdSe and CdSe–Au interfaces are identical in the TiO₂–CdSe–Au photoelectrode, which promotes the separation of photogenerated excitons and subsequently enhances their transportation for enlarged photocurrent density. The results of photoelectrocatalytic hydrogen production also confirm our assumption.     

Novel luminescent heterobimetallic Ln–Cu(I) 3D coordination polymers based on 5-(4-pyridyl) isophthalic acid as heteroleptic ligand. Synthesis and structural characterization

Six novel photoluminescent Ln–Cu(I) heterobimetallic 3D coordination polymers, [LnCu (pyip^2 −)₂(H₂O)]_n (1–6) (where Ln is Pr, Nd, Sm, Eu, Gd, Ho, respectively, and H₂pyip = 5-(4-pyridyl) isophthalic acid) have been synthesized in a concise and reproducible manner under hydrothermal conditions. All of these substances were fully characterized by appropriate spectroscopic methods and elemental analysis. Structural determinations revealed that 1–6 are isomorphic and display 3D frameworks. Luminescent properties of the obtained compounds have been studied in detail revealing light emissions of warm white, cool white and light blue for 3, 4 and 5, respectively. The effectiveness of association of a rare earth with a transition metal in producing valuable luminescent materials for practical applications is demonstrated.     

Two phenoxo-O bridged Dy2 complexes based on 8-hydroxyquinolin derivatives with different magnetic relaxation features

Two new dinuclear dysprosium compounds, namely, [Dy₂(L1)₂(hfac)₆]·C₇H₁₆ (1) and [Dy₂(L2)₂(hfac)₆]·C₇H₁₆ (2) (HL1 = 5-(2-thenylidene)-8-hydroxylquinoline; HL2 = 5-(4-methoxylbenzylidene)-8-hydroxylquinoline; hfac = hexafluoroacetylacetonate) have been successfully obtained via applying two different ligands, and further characterized by crystallography. Structural analysis shows that both of 1 and 2 possess a four-membered [Dy₂O₂] core with similar coordination pockets. The center Dy(III) ions in 1 and 2 are all completed by eight coordination environments with O₈ set. Interestingly, the different features of ligand HL1 and HL2 result in their different magnetic relaxation behaviors with the energy barrier of 6.81 K for 1 and 0.72 K for 2.     

Effects of specimen and grain sizes on compression strength of annealed wrought copper alloy at room temperature

Variations in compression yield strength of annealed wrought CuAl7 copper alloy with specimen diameter (t) in 1–10 mm range and grain size (D) in 24–172 μm range were investigated. Both grain size effect and feature size effect could be observed. The compression yield strength increased with a reduction in grain size or specimen diameter, and varied with the t/D ratio in no particular manner. However, when t was held constant, the compression yield strength increased as the ratio increased. When D was held constant, the strength decreased as the ratio increased. The Hall–Petch relationship between the compression yield strength and the grain size was found to depend on the specimen diameter. The effect of feature size was greater than that of grain size. A new model of the relationship between the compression yield strength and the grain size, specimen diameter, and size factor has been built. The predicted results of the model agreed well with the experimental results. The fit of the model was better than that of a model based on the relationship between the compression yield strength and the grain size and specimen diameter only.