Experimental study of culture for mouse fibroblast used conductive polymer films

The purpose of this study is to develop electrodes for electrical stimulation of the nervous system using conductive polymers, polypyrrole (PPy) and/or poly(3,4-ethylenedioxythiophene), PEDOT. We evaluated biocompatibility in fibroblast and/or myoblast of mouse. Cultured cells on PPy and/or PEDOT extended their neuritis and survived over a week. These experiments have demonstrated that conductive polymers such as PPy, PEDOT, etc. have high biocompatibility, and PPy and/or PEDOT are applicable to nerve stimulation electrodes.     

Rapid erasing of wettability patterns based on TiO2-PDMS composite films

TiO₂-polydimethylsiloxane (TiO₂-PDMS) composite films are prepared using the sol–gel method from a Ti(OBu)₄–benzoylacetone solution containing PDMS. The prepared films are cured by irradiation with ultraviolet (UV) light. Structural changes in the films after UV irradiation are confirmed by UV–vis absorption experiments, which show that an absorption band characteristic of the benzoylacetonate chelate rings disappears. This finding is ascribed to structural changes associated with the dissociation of the chelate rings. The IR spectra of the thin films exhibit a broad absorption band after UV irradiation, indicating that a Ti–O–Ti network forms in the thin film. Contact angles are measured for the TiO₂-PDMS thin films, showing wettability conversion from hydrophobic to superhydrophilic states by irradiation with oxygen plasma for 1 s. This phenomenon is explained by XPS experiments which reveal that the number of carbon atoms decreases, whereas the number of oxygen atoms increases on the surface of the TiO₂-PDMS composite films. Finally, hydrophobic–superhydrophilic patterns are fabricated based on a patterned TiO₂-PDMS composite film. The film displays a rapid change to superhydrophilicity over the whole film surface upon plasma irradiation for 1 s, which means that the wettability patterns are rapidly erasable.     

Fabrication of discrete polystyrene nanoparticle arrays with controllable their structural parameters

We have demonstrated the fabrication of two-dimensionally periodic non-close packed arrays of spherical polystyrene nanoparticles with controllable their structural parameters including diameter and interpartcile distance. The principle of this procedure relies on stepwise integration of spin-coat-assisted colloidal self-assembly of the single layer of close-packed polystyrene nanoparticle on a substrate, and subsequent etching of the particle under atmospheric pressure helium plasma. The plasma process converted the close-packed nanoparticle array into non-close-packed arrangement remaining with unchanged their original spherical shape and periodicity. Owing to the etching process underwent isotropically, the structural parameters could be controlled with nanometric accuracy by the treatment time. The etching rate strongly depended on the working pressure conditions, and the etching rate under 250 Torr was ca. 3 times faster than that of the 760 Torr. The effects of the working pressure indicated the neutral helium radicals and photons diffused from the plasma might be primarily responsible for the etching.     

Finishing of AT-cut quartz crystal wafer with nanometric thickness uniformity by pulse-modulated atmospheric pressure plasma etching

Quartz resonator is a very important device to generate a clock frequency for information and telecommunication system. Improvement of the productivity of the quartz resonator is always required because a huge amount of the resonator is demanded for installing to various electronic devices. Resonance frequency of the quartz resonator is decided by the thickness of the quartz crystal wafer. Therefore, it is necessary to uniform the thickness distribution of the wafer with nanometric level. We have proposed the improvement technique of the thickness distribution of the quartz crystal wafer by numerically controlled correction using atmospheric pressure plasma which is non-contact and chemical removal technique. Heating effects of the quartz wafer in the removal rate and the correction accuracy were investigated. The heating of the substrate and compensate of the scanning speed of the worktable according to the variation of the surface temperature enabled an increase of 50% in the etching rate and 10-nanometric-level accuracy in the correction of the thickness distribution of the quartz wafer, respectively.     

Development of Concrete Bridge Rating Prototype Expert System with Machine Learning

Efforts to develop practical expert systems have mostly concentrated on how to implement experience-based machine learning successfully. Recently several active research projects on machine learning have been undertaken from the viewpoint of knowledge-based management. The aim of this study is to develop the Concrete Bridge Rating (Diagnosis) Prototype Expert System with machine learning, employing the combination of a neural network and bidirectional associative memories (BAM). The introduction of machine learning into this system facilitates knowledge-based refinement. By applying the system to an actual in-service bridge, it has been verified that the machine learning method employed that uses the results of questionnaire surveys involving bridge experts is effective for the system.     

粉末冶金结构零件材料的泊松比

研究了粉末冶金机械零件使用的烧结材料的杨氏模量、切变模量及泊松比与孔隙度的关系.制备了三种钢粉,在不同条件下进行了压制、烧结与热处理.孔隙度对杨氏模量、切变模量及泊松比的影响最大.特别是泊松比还受孔隙形状的影响,而孔隙形状随粉末类型、烧结温度与烧结气氛及热处理条件而变化.对于大部分实际应用的粉末组成来说,烧结气氛对经烧结和热处理后材料的泊松比影响不大.对于部分预合金化粉末(Fe4%Ni1.5%Cu0.5%Mo)+0.8%石墨,只有在孔隙度低于20%时,烧结温度对泊松比与孔隙度的关系才有影响.在这种情况下.提出了烧结与热处理试样泊松比与孔隙度关系的较简单近似方程:在烧结温度1 423K下,v=0.300-0.266P+0.579P2;在烧结温度1 523K下,v=0.304-0.264P+0.548P2.     

Electrophoretic deposition of conjugated polymer: Deposition from dilute solution and PEDOT coating effect

It has been shown that the films of a soluble conjugated polymer poly[(9,9-dioctyl-2,7-divinylene fluorenylene)-alt-{2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylene}] for electronic devices can be prepared by the electrophoretic deposition with polymer suspensions derived from dilute polymer solutions which are so dilute that the conventional spin-coating technique is not applicable. For example, a 100 nm-thick film can be prepared on an indium-tin-oxide (ITO) electrode from a suspension from solution containing 0.1 g/l of the polymer. The thickness of the polymer film deposited is found to be almost proportional to the concentration of the polymer, and the linearity down to 5.0 × 10^?3 g/l is confirmed. On the other hand, it has been found that coating the ITO electrode with poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) salt results in low and nonlinear deposition rate.     

Anionic alternating copolymerization of epoxide and 3,4‐dihydrocoumarin and its application to networked polymers

3,4‐Dihydrocoumarin (DHCM) is an aromatic six‐membered lactone, which does not undergo anionic homopolymerization. However, it does undergo copolymerization with an epoxide. The striking feature of this copolymerization is its 1:1 alternating nature, which allows for the formation of polyesters. In this mini‐review, we describe the copolymerization behavior, the polymer structure and the advantages that can be achieved by addition of DHCM to the epoxy‐imidazole curing system. Another focus is our development of DHCM analogues, which bring the advantages of DHCM to their applications as comonomers for the curing system. Copyright © 2009 Society of Chemical Industry     

Biocompatibility of a-C:H film coating for synthetic vascular graft

Amorphous hydrogenated carbon (a-C:H) films have many excellent properties such as biocompatibility, anti-corrosion, and chemical stability. Therefore, there are many reports on application of a-C:H film as surface modification technique for biomaterials. However, it is difficult to deposit a-C:H film on complex structures such as artificial heart blood pump and synthetic vascular grafts. In our previous work, we have developed an electrode which is adapted to such irregular structures for plasma CVD technique.In this study, a-C:H film was deposited on a synthetic vascular graft inner-wall by r.f. plasma CVD technique with cylindrical electrode. The purpose of such coating is improvement of biocompatibility of the vascular graft. The biocompatibility of the a-C:H film was evaluated by cytocompatibility and plasma protein adhesion. For the a-C:H film deposition, cytocompatibility and protein adsorbent of the vascular grafts were improved for biological response under cell culture with mouth fibroblasts and plasma proteins (albumin, fibrinogen, and globulin), respectively. This study indicates that the a-C:H films coatings is expected to surface modification for medical appliances.