三聚氰胺基螯合树脂/碳纳米管修饰充蜡石墨电极阳极溶出伏安法测定铅和镉

采用超声法合成了三聚氰胺-甲醛-硫脲螯合树脂（MFT）,基于碳纳米管优良的光电性能,制备了MFT/纳米碳管复合物修饰充蜡石墨电极（MFT/MWCNTs/WGE）。 采用场发射扫描电子显微镜及电化学技术表征了该修饰电极的特性。 该电极被成功地用于水溶液中重金属离子Pb(Ⅱ)和Cd(Ⅱ)的同时测定,Pb(Ⅱ)和Cd(Ⅱ)的溶出峰电流与浓度分别在3×10-8～9×10-7 mol/L和5×10-8～7×10-7 mol/L的浓度范围内,呈良好的线性增长关系,Pd(Ⅱ)和Cd(Ⅱ)的检测限分别为2×10-9和3×10-9 mol/L（3σ）。     

宏观共振隧穿的新进展及其在量子信息处理中的应用

从量子力学诞生以来,关于宏观物体的运动是否遵循量子力学的辩论就一直没有停止过.上世纪八十年代初期以来,一系列在约瑟夫森结和超导最子干涉器件(SQUID)中观测到的实验结果,包括相位和磁通的宏观量子隧穿,能级量子化,宏观共振隧穿,和在微波驱动下的相干动力学过程对认为宏观物体的运动在满足一定条件下同样遵循量子力学规律的观点提供了强有力的实验证据.在众多已观察到的宏观量子现象中,宏观共振隧穿结合了能级分立和隧穿这两个最具特征的量子现象.由于宏观共振隧穿的观测无需使用高频电磁波激发,这就避免了实验结果也可以用经典物理解释的可能,所以在一个系统中观测到宏观共振隧穿可以说是展示该系统的量子属性的最有力证据.本文讨论近年来从理论和实验两方面理解耗散和磁通噪声对类似SQUID的双势阱系统宏观共振隧穿率和谱线形状的影响.评述宏观共振隧穿谱的测量在探寻、理解、克服超导磁通量子比特中的退相干机制并最终实现规模化量子计算方面的应用.     

时效处理对AA2099铝锂合金摩擦学行为的影响

研究了固溶及不同时效状态AA2099铝锂合金的力学性能、摩擦学行为及机理.结果表明:随时效时间的延长,摩擦系数先降低后升高,时效35 h时摩擦系数最低(0.137);磨损量单调减少,时效96 h合金的磨损率最低,为1.7×10–3 mm3/(N·m).固溶态和不同时效态的AA2099铝锂合金主要磨损机制均为磨粒磨损和黏着磨损.摩擦产物对摩擦系数有重要影响,时效35 h的合金摩擦产物分布均匀且连续,具有良好的减摩作用;合金的力学性能与磨痕浅层结构稳定性共同影响合金的磨损率,时效时间小于35 h,合金表面易形成发生剥落的结构,磨损量变化与传统认为的H/E变化不符,但随时效时间进一步延长,剥落减少,磨损量与H/E变化正相关.     

Modelling of pressure–strain correlation in compressible turbulent flow

Previous studies carried out in the early 1990s conjectured that the main compressible effects could be associated with the dilatational effects of velocity fluctuation. Later, it was shown that the main compressibility effect came from the reduced pressure-strain term due to reduced pressure fluctuations. Although better understanding of the compressible turbulence is generally achieved with the increased DNS and experimental research effort, there are still some discrepancies among these recent findings. Analysis of the DNS and experimental data suggests that some of the discrepancies are apparent if the compressible effect is related to the turbulent Mach number, Mt. From the comparison of two classes of compressible flow, homogenous shear flow and inhomogeneous shear flow （mixing layer）, we found that the effect of compressibility on both classes of shear flow can be characterized in three categories corresponding to three regions of turbulent Mach numbers： the low-Mr, the moderate-Mr and high-Mr regions. In these three regions the effect of compressibility on the growth rate of the turbulent mixing layer thickness is rather different. A simple approach to the reduced pressure-strain effect may not necessarily reduce the mixing-layer growth rate, and may even cause an increase in the growth rate. The present work develops a new second-moment model for the compressible turbulence through the introduction of some blending functions of Mt to account for the compressibility effects on the flow. The model has been successfully applied to the compressible mixing layers.     

Monitoring the Structure Evolution of Titanium Oxide Photocatalysts: From the Molecular Form via the Amorphous State to the Crystalline Phase

Amorphous Ti_xO_y with high surface area has attracted significant interest as photocatalyst with higher activity in ultraviolet (UV) light-induced water splitting applications compared to commercial nanocrystalline TiO₂. Under photocatalytic operation conditions, the structure of the molecular titanium alkoxide precursor rearranges upon hydrolysis and leads to higher connectivity of the structure-building units. Structurally ordered domains with sizes smaller than 7 Å form larger aggregates. The experimental scattering data can be explained best with a structure model consisting of an anatase-like core and a distorted shell. Upon exposure to UV light, the white Ti_xO_y suspension turns dark corresponding to the reduction of Ti⁴⁺ to Ti³⁺ as confirmed by electron energy loss spectroscopy (EELS). Heat-induced crystallisation was followed by in situ temperature-dependent total scattering experiments. First, ordering in the Ti−O environment takes place upon to 350 °C. Above this temperature, the distorted anatase core starts to grow but the structure obtained at 400 °C is still not fully ordered.     

Assembly‐Induced Emission of Cellulose Nanocrystals for Hiding Information

Fluorescent‐labeled cellulose nanocrystal (CNC) films have been used to record and protect information in paper materials, whereas the fluorescent materials usually suffer photobleaching. Herein, a strategy of solid‐state emission induced by the vertical assembly of CNCs was established. The assembly‐induced emission starts from the structural diffraction of CNC, whose wavelength is adjusted into the ultraviolet (UV) region for hiding information under natural light. The small diameter (≈10 nm) of CNCs then promotes the resonance between the vertically assembled CNCs and the UV light, leading to a strong blue emission with an emitting quantum efficiency as high as 13.90%. By introducing the vertical‐assembly film with a specific pattern into paper materials, an anti‐counterfeiting image is obtained under a UV radiation. Since CNCs are a kind of cellulose with high crystallinity, this material can be a wear‐resistant anti‐counterfeiting material for banknotes or other paper applications.     

Influence of embedded boron nitride nanosheets on Fe3+ diffusion in Fricke gel dosimeter and its response to γ rays

Journal of Radioanalytical and Nuclear Chemistry - The Fe3+ diffusion in Fricke gel dosimeter, widely used for the measurement of accurate dose distributions in radiotherapy, results in a gradual...     

Recyclable helical poly(phenylacetylene)‐supported catalyst for asymmetric aldol reaction in aqueous media

A novel one‐handed helical poly(phenylacetylene) bearing L‐hydroxyproline pendants (poly(PA‐P)) was synthesized as an eco‐friendly polymer‐supported catalyst for asymmetric reactions. The helical poly(PA‐P) catalyzed the asymmetric aldol reactions of cyclohexanone with p‐nitrobenzaldehyde, and showed good recyclability and higher enantiomeric excess (ee) in aqueous medias than that in organic medias. The one‐handed helicity of poly(PA‐P) was clearly affected by the water content in the aqueous media. The helical poly(PA‐P) showed the higher enantioselectivity (ee = 99%) than its monomer PA‐P (ee = 54%) in THF/H₂O (H₂O vol % = 25.0 vol %). After the one‐handed helical structure of poly(PA‐P) was destroyed by grinding treatment, the ee of the reaction clearly decreased from 99 to 49%. These indicate that the one‐handed helical structure of poly(PA‐P) played an important role in the high enantioselectivity of the asymmetric aldol reactions in the aqueous media. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 1024–1031     

利用新型生物聚酯P3HB4HB构建原位催化NO生成人工血管材料

以新型生物聚酯P3HB4HB静电纺丝纤维支架材料为基质,通过层-层自组装技术向基质中引入γ-聚谷氨酸和聚赖氨酸,并负载含硒催化剂硒代胱胺,构建具有催化NO原位生成功能的人工血管材料,通过体外催化释放NO实验、细胞毒性检测、平滑肌细胞铺展实验考察人工血管材料的生物功能。实验结果表明,该材料具有良好的纤维多孔结构,适于作血管支架材料;通过控制有机硒的负载量可调控NO催化生成速率;而且该材料具有良好的生物相容性,能够有效抑制平滑肌细胞的黏附与铺展。     

碳纳米管@碳化硅同轴异质结纳米管非金属光催化剂产氢性能（英文）

近年来,光催化裂解水产氢(H2)引起了广泛的关注.储量丰富,环境友好的非金属无机半导体β-SiC(立方相碳化硅)具有适当的带隙(Eg=2.4 eV,ECB=?0.9 V),是一种潜在的光催化剂.受限于SiC光催化剂内部光生电子-空穴对的快速复合,SiC光催化剂的效率较低.已有的关于SiC光催化剂改性的报道主要包括构建纳米SiC,构建SiC异质结,构建碳/SiC材料杂化材料.进一步的研究表明,SiC与碳材料之间通过紧密的界面接触形成了肖特基结,能将SiC表面的光生电子快速转移,抑制光生电子-空穴对的快速复合,从而提高光催化分解水产氢的活性.另一方面,碳纳米管(CNTs)具有良好的电子导电性,一维有序的管腔所形成的电子快速传导路径.因此,将半导体光催化剂与CNTs复合,是一种制备先进的光催化剂的有效策略.本文利用Si蒸气与CNTs之间的气-固反应,在CNTs表面原位生长SiC纳米包覆层,成功地制备了一维同轴核-壳CNTs@SiC纳米管.高分辨率透射电子显微镜图像表明,SiC与CNTs之间是通过Si-C共价键原子接触,并得到X射线光电子能谱的证实.将一部分CNTs@SiC纳米管在空气中750 oC煅烧2 h以除去CNTs,得到纯SiC纳米颗粒作为对比组.紫外-可见吸收光谱表明,CNTs能够促进SiC对光的吸收.荧光发射光谱(PL),瞬态荧光寿命测试,瞬态光电流测试以及交流阻抗(EIS)测试表明,CNTs能够促进SiC表面光生电子的传输与分离,有利于提升光催化效率.以0.1 mol/L Na2S溶液作为牺牲剂,在模拟太阳光(A.M 1.5)照射下,CNTs@SiC纳米管(不额外负载Pt等贵金属作为助剂)的产氢速率为118.5μmol g^-1 h^-1,是纯SiC纳米颗粒(21.1μmol g^-1 h^-1)的5.62倍.经过20 h的光照测试,CNTs@SiC纳米管的光催化性能无明显衰减;X射线衍射测试与扫描电子显微镜图像表明,CNTs@SiC纳米管的结构与形貌反应前后几乎无变化.莫特-肖特基测试表明,CNTs的费米能级比SiC低,因此SiC表面的光生电子能够快速地转移到CNTs,并且CNTs的良好导电性与一维有序的管腔所形成的长的电子传导路径能够进一步地增加电子寿命,促进光生电子参与光催化反应.另外,通过原子连接的同轴核-壳CNTs@SiC纳米管提供了大量且有效的电子传输路径.因此,与纯SiC纳米晶等同类材料相比,无机非金属CNTs@SiC纳米管具有更强的光催化氢活性.