Experimental study to assess the effect of carbon nanotube addition on the through-thickness electrical conductivity of CFRP laminates for aircraft applications

The present paper tests experimentally the through-thickness electrical conductivity of carbon fiber-reinforced polymer (CFRP) composites laminates for aircraft applications. Two types of samples were prepared: Type A samples with carbon nanotubes (CNTs) and Type B samples without CNTs. During the electrical experiments, electrical currents of several mA were injected through the specimens. Electrical resistance was monitored simultaneously in order to deduce the changes in the through-the-thickness electrical conductivity caused by the addition of CNTs. Improvement of electrical conduction by two orders of magnitude was achieved through the addition of 1 wt% carbon nanotubes as compared to classic CFRP without CNTs. For moisture saturated samples, the influence of moisture absorption on such measures was found to be negligible.     

Templated titania films with meso- and macroporosities

Porous TiO₂ films with both mesoporosity and macroporosity were fabricated by a templated sol–gel method for applications, such as dye-sensitized solar cells (DSC), photocatalysis and catalysis. With the incorporation of differently sized pores, the resultant structures exhibit high surface areas and possess interpenetrating aligned pore channels, which are believed to be beneficial for applications where diffusion of reactants to interior surface can be rate limiting. Both liquid and solid TiO₂ precursors can be applied for large area coating in this process. Almost crack-free films were produced by templated coating of pre-synthesized TiO₂ nanoparticles. The measured specific surface area and porosity of synthesized films were in the range of 33–137 m²/g and 61–80%, respectively, depending on the size of the selected template.     

Preparation and adsorption behavior of a cellulose‐based,mixed‐mode adsorbent with a benzylamine ligand for expanded bed applications

A novel mixed‐mode expanded bed adsorbent with anion‐exchange properties was explored with benzylamine as the functional ligand. The cellulose composite matrix, densified with stainless steel powder, was prepared with the method of water‐in‐oil suspension thermal regeneration. High activation levels of the cellulose matrix were obtained with allyl bromide because of the relative inertness of the allyl group under the conditions of the activation reaction. After the formation of the bromohydrin with N‐bromosuccinimide and coupling with benzylamine, the activated matrix was derived to function as a mixed‐mode adsorbent containing both hydrophobic and ionic groups. The protein adsorption capacity was investigated with bovine serum albumin as a model protein. The results indicated that the prepared adsorbent could bind bovine serum albumin with a high adsorption capacity, and it showed salt tolerance. Effective desorption was achieved by a pH adjustment across the isoelectric point of the protein. The interactions between the cell and adsorbent were studied, and the bioadhesion was shielded by the adjustment of the salt concentration above 0.1M. Stable fluidization in the expanded bed was obtained even in a 2% (dry weight) yeast suspension. The direct capture of target proteins from a biomass‐containing feedstock without extra dilution steps could be expected with the mixed‐mode adsorbent prepared in this work, and this would be especially appropriate for expanded bed adsorption applications. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Synthesis,structure and near-infrared (NIR) luminescence of three solvent-induced pseudo-polymorphic complexes from a bimetallic Zn–Nd Schiff-base molecular unit

Three solvent-induced pseudo-polymorphic bimetallic Zn–Nd complexes [ZnNdL(OAc)(NO₃)₂(DMF)] · solvate (solvate: MeCN (1), THF (2), EtOH (3); H₂L = N,N′-bis(3-methoxy-salicylidene)phenylene-1,2-diamine) were obtained, and their solid NIR luminescence related to the packing structure from the intermolecular π–π interactions was discussed.     

The miR-106b/NR2F2-AS1/PLEKHO2 Axis Regulates Migration and Invasion of Colorectal Cancer through the MAPK Pathway

Increasing numbers of miRNAs have been observed as oncogenes or tumor suppressors in colorectal cancer (CRC). It was recently reported that hsa-miR-106b-5p (miR-106b) promoted CRC cell migration and invasion. However, there were also studies showing contradictory results. Therefore, in the present study, we further explore the role of miR-106b and its downstream networks in the carcinogenesis of CRC. We observed that the expression of miR-106b is significantly increased in Pan-Cancer and CRC tissues compared with normal tissues from The Cancer Genome Atlas (TCGA) database. Furthermore, we used Transwell, Cell Counting Kit-8, and colony formation assays to clarify that miR-106b promotes the migratory, invasive, and proliferative abilities of CRC cells. For the first time, we systematically screened the target mRNAs and lncRNAs of miR-106b using TCGA database and the bioinformatics algorithms. Dual-luciferase reporter assay confirmed that NR2F2-AS1 and PLEKHO2 are the direct targets of miR-106b. Furthermore, NR2F2-AS1 acts as a competing endogenous RNA (ceRNA) to regulate PLEKHO2 expression by sponging miR-106b. The results of Gene set enrichment analysis (GSEA) and Western blot indicated that they play important roles in CRC progression by regulating MAPK pathway. Thus, miR-106b/NR2F2-AS1/PLEKHO2/MAPK signaling axis may suggest the potential usage in CRC treatment.     

Natural Polysaccharides as Multifunctional Components for One-Step 3D Printing Tough Hydrogels

Natural polysaccharides (NPS) are regarded as biomolecular and structural components for preparing high-performance tough hydrogels. But the one-step fabrication of NPS-containing hydrogels in seconds and the template-free design of complicated high-resolution structures are still significant challenges in this field. To meet these requirements, various NPS-containing tough hydrogels are fabricated and processed into 2D/3D structures via the combination of Ru(bpy)₃²⁺-mediated photochemistry and extrusion 3D printing technique. The whole fabrication process is one-step, completed in tens of seconds under visible light irradiation. It is found that the used NPS plays a key role in achieving the fabrication of high-performance structured tough hydrogels. The high reactivity of functional groups in the used NPS can shorten their gelation times. Long rigid chains of the used NPS, their hierarchical assemblies, and contrasting multinetworks benefit from the efficient dissipation of mechanical energy and enhancement of its operational stability. Strong supramolecular interactions enable hydrogel precursors to have high viscosities, therefore providing good controllability to design high-resolution and complicated tough hydrogel structures via extrusion 3D printing. It is anticipated that this straightforward fabrication strategy and findings will open new horizons for NPS-containing materials.     

论我国证券经纪制度创新的模式选择

面对当前全球证券市场发展前景,我们应当以国内外成熟经纪人制度为典范,寻求适合我国证券市场特点的经纪制度模式。我国金融市场处于落后水平,要发展经纪人必须提高经纪人的专业素质、降低职业道德风险,以此为切入点,通过对我国××证券公司经纪人队伍建设的研究,提出我国证券经纪人制度创新的模式设想,以期早日打开证券经纪人产业的大门。     

凝胶法制备纳米氧化锌颗粒及其光谱分析

就尝试利用溶胶-凝胶法制备纳米氧化锌颗粒,并且运用各种表征技术和测试手段(扫描电镜(SEM)及X射线衍射技术(XRD))对所制备的纳米材料进行了表征、分析和性能研究,主要得出以下结论:(1)验证纳米氧化锌是纤锌矿结构,以六边形貌存在。(2)观察到氧化锌的光谱图与已知的氧化锌的光谱图一致。并且看出不同烧结温度对它的光谱有一定的影响。(3)氧化锌在不同波长的激发下所得到的光谱与现有理论保持一致,这也再一次验证了理论的正确性。     

An unusual 3D three-fold parallel interpenetrating network self-assembled from the grid-containing 2D layer motifs

The new complex {[Cu(dde)(bpe)] · H₂O}_n (1) (dde = 4,4′-dicarboxydiphenyl ether, bpe = 1,2-bis(4-pyridyl)ethene) has been synthesized and characterized. It exhibits a novel (2D → 3D) three-fold parallel interpenetrating architecture that is obtained for the first time from the self-assembly of grid-containing 2D (4, 4) layer motifs. The fluorescent property of 1 is discussed.