Feasibility study on cellular network analysis with patterned cell culture microdevice

In order to realize cellular network analysis on a chip-based system, our group has been developing a patterned cell culture microdevice with pillars in an array for tapping cells into space surrounded by the pillars. The pillar structures has advantages to trap both adhesive and non-adhesive cells and to precisely control positions of cells and distances between cells for understanding effects of various cell patterns on functions of a cellular network such as cell proliferation, differentiation, and network formation. In this paper, HeLa cell cultivation with the patterned cell culture microdevice having a pillar array fabricated by dry film of thick negative photoresist SU-8 on a glass substrate was executed as a feasibility study on a cellular network analysis. The results revealed that the device performance was found to be enough to culture HeLa cells for more than 48 h. In addition, relative extensibility of blocks of multiple cells compared with single cells tapped on the device was observed. Thus, the patterned cell culture microdevice proposed here could be applicable to analysis of cellular functions.     

Dielectric properties of woven fabric glass fiber reinforced polymer-matrix composites in the THz frequency range

Electromagnetic wave transmittances of plain woven fabric glass fiber reinforced epoxy matrix composite (PW-GFRP) and eight-harness-stain fabric glass fiber reinforced polyimide matrix composite (8H-GFRP) with 1.0 mm thickness were measured in a terahertz (THz) frequency range. The transmittance values for both composites are nearly zero at a frequency of 1.0 THz. The real parts of the complex dielectric constant, ε′(ω) are 4.45 and 3.87 for PW-GFRP and 8H-GFRP, respectively, in the frequency range from 0.2 to 1.0 THz, and they are almost frequency independent. Conversely, the imaginary parts of the dielectric constant, ε′′(ω) for both composites linearly increases with increase of the frequency from 0.13 to 0.37 for PW-GFRP, and from 0.12 to 0.33 for 8H-GFRP.     

An Intrinsically Fluorescent Recognition Ligand Scaffold Based on Chaperonin Protein and Semiconductor Quantum‐Dot Conjugates

Genetic engineering of a novel protein–nanoparticle hybrid system with great potential for biosensing applications and for patterning of various types of nanoparticles is described. The hybrid system is based on a genetically modified chaperonin protein from the hyperthermophilic archaeon Sulfolobus shibatae. This chaperonin is an 18‐subunit double ring, which self‐assembles in the presence of Mg ions and ATP. Described here is a mutant chaperonin (His‐β‐loopless, HBLL) with increased access to the central cavity and His‐tags on each subunit extending into the central cavity. This mutant binds water‐soluble semiconductor quantum dots, creating a protein‐encapsulated fluorescent nanoparticle. The new bioconjugate has high affinity, in the order of strong antibody–antigen interactions, a one‐to‐one protein–nanoparticle stoichiometry, and high stability. By adding selective binding sites to the solvent‐exposed regions of the chaperonin, this protein–nanoparticle bioconjugate becomes a sensor for specific targets.     

铝合金与不锈钢大气钎焊性的改善——铝合金与不锈钢焊接技术(二)

在基本查明铝合金与不锈钢焊接困难原因的基础上,参考钎料对纯铝等温凝固过程的数值解析以及熔融钎料层消失时间的推定及试验结果,探讨了解决对策.采用电阻炉、TCM10000万能试验机进行了钎焊接头改善及评价试验,以此为依据提出了改善铝合金与不锈钢钎焊性的新焊接方法,即增大钎焊间隙实施钎焊的方法;预先使钎料对不锈钢产生润湿,然后再与铝合金实施钎焊的方法.又采用上述方法进行了其它形状部件的制作,从理论到实践验证了新焊接方法的可行性.     

Separation of PRMMC into matrix alloy and reinforcements by nozzle filtering method

The SiC_P/Al–4 mass%Cu alloy composites fabricated by a low-pressure infiltration process (LPI process) were remelted and separated by nozzle filtering method. In the separation process, the PRMMC specimen was placed in a container with a small nozzle at the bottom. The molten PRMMC was forced to flow out through the nozzle by applying a certain pressure of Ar gas. Most of the molten matrix alloy flowed out through the nozzle and the remainder in the container consisted of SiC particles and a part of the matrix alloy. The particle volume fraction of the remainder was higher than that of the original PRMMC and the remainder would work as a filter to separate SiC particles from the matrix alloy melt. When nozzle tip angle was ranged from 60° to 120°, about 80% of matrix alloy in the PRMMC was separated and few SiC particles were observed in the separated matrix alloy. The surface of recovered SiC particles became slightly roughened due to the reaction with the molten matrix during the separation process. However, this is not expected to affect their reuse.     

Properties of bifunctional phosphonate fibers derived from chloromethylstyrene grafted polyolefin fibers

Bifunctional fibers containing phosphonate and sulfonate were derived from chloromethylstyrene grafted polyolefin fibers (PPPE-g-CMS) by phosphorylation and subsequent sulfonation reactions. It was clarified that phosphorylation of PPPE-g-CMS by Arbusov reaction is more suitable than one by the reaction with PCl₃ in the presence of AlCl₃, because the latter damaged fibers and gave phosphinate groups in addition to phosphonate ones. Then, bifunctional fibers containing phosphonate and sulfonate groups were prepared by sulfonation of monofunctional phosphonate fibers obtained via Arbusov reaction with chlorosulfonic acid. The metal ion selectivity of the bifunctional fibers was governed by both phosphonate and sulfonate groups. In addition, bifunctional fibers gave much more excellent kinetic performances in column-mode uptake of Cu(II) than the monofunctional phosphonate fibers and resin.     

One-step formation of ethyl methyl ketone from 1-butene and water on ultrastable Y-type zeolite catalyst

Proton exchanged ultrastable Y-type zeolite with silica/alumina = 40 showed a pronounced catalytic activity for the formation of ethyl methyl ketone directly from 1-butene and water. The formation rate of ethyl methyl ketone was much higher than those on MoO₃-based catalysts in the oxidation of 1-butene by oxygen. It was suggested that the basic site necessary for the formation of ethyl ketone directly from 1-butene and water would be the pentacoordinated Al.     

Pyrolysis of melamine–formaldehyde and urea–formaldehyde resins

Pyrolysis of melamine–formaldehyde and urea–formaldehyde resins in helium and air was investigated by means of TG and gravimetry with isothermal heating, as well as elemental and HCN analyses. Weight loss curves suggest three kinds of reactions involved in the pyrolysis, namely, initiation reactions, reactions splitting off volatile fragments, and reactions forming stabilized structures. In TG, in both helium and air atmospheres, the active weight loss of the melamine resin was completed in two steps, and that of the urea resin was completed in one step, which, however, consisted of a few small successive steps. The isothermal heating weight losses progressed through a few stages of first- and zeroth-order reactions. Arrhenius parameters were obtained for the weight losses in TG and with isothermal heating. The residue from the melamine resin is rich in carbon and nitrogen, and poor in oxygen and hydrogen, while that from the urea resin is rich in carbon, and poor in nitrogen, oxygen, and hydrogen. The effects of temperature on HCN yield changed, depending on the amount of air fed. The melamine resin evolved much more HCN than the urea resin because of the more stable C—N linkages in the resin.     

Development of a new advanced process for manufacturing polyacetal resins. Part III. End-capping during polymerization for manufacturing acetal homopolymer and copolymer

Conventionally, acetal homopolymer or copolymer is obtained by the polymerization of formaldehyde or trioxane, following the end-capping using acetic anhydride or unzipping of the unstable polymer end fraction. First, Asahi Chemical developed a new process to obtain an end-capped polymer during polymerization of highly purified formaldehyde using acetic anhydride as the chain-transfer agent. Use of highly purified formaldehyde and endcapping during polymerization using acetic anhydride as a chain-transfer agent or an endcapping agent will provide a simple process for manufacturing acetal homopolymer. The polymerization mechanism was confirmed by infrared spectroscopy analysis and proton NMR analysis of the polymer obtained. Second, for the acetal copolymer, purified trioxane was copolymerized with ethylene oxide in the presence of methylal, which gave an endcapped polymer with high thermal stability. Two new intermediates from the initiation reaction of the copolymerization, 1,3,5,7-tetraoxacyclononane (TOCN) and 1,3,5,7,10-pentaoxacyclododecane (POCD), were isolated and a new initiation mechanism was proposed. © 1993 John Wiley & Sons, Inc.     

Formation and Crystallization of Yttrium Aluminosilicate Glasses Containing Calcium Oxide

Formation of yttrium aluminosilicate glasses containing calcium oxide from batches melted at 1550°C was investigated. Densities and thermal expansion coeflcients were measured for some glasses. In a specific compositional region, crystals with a needlelike habit were observed in the glass matrix. A crystal in the form of a tubular hexagonal prism was identified as Ca₄Y₆0(Si0₄)₆.