Fabrication of miniature Clark oxygen sensor integrated with microstructure

A miniature Clark-type oxygen sensor has been integrated with a microstructure using a novel fabrication technique. The oxygen chip consists of a glass substrate with a three-electrode configuration, which is separated and connected by a groove, and a poly(dimethylsiloxane) (PDMS) container with an immobilized PDMS oxygen-permeable membrane. The assembly of the different substrates only uses the O₂ plasma bonding technique, and the fabrication temperatures do not exceed 95 °C. Characteristics of the miniature sensor include the fastest response time of 6.8 s, good linearity with a correlation coefficient of 0.995, and a long lifetime of at least 60 h. The present miniature Clark oxygen sensor can be readily integrated with a microfluidic system to form a μ-TAS.     

A novel anisotropic conducting thin film having a conducting and insulating layered structure

Electrochemical polymerization of Langmuir-Blodgett multilayers of amphiphilic pyrrole derivatives resulted in novel anisotropic conducting thin films (T. Iyoda, M. Ando, T. Kaneko, A. Ohtani, T. Shimidzu and K. Honda, Tetrahedron Lett., 27 (1986) 5633). They have an alternating layered structure of a conducting polypyrrole layer and an insulating alkyl chain layer. This paper deals with their syntheses, characterizations and functionalities.     

Removal of formaldehyde from gas phase by silylated graphite oxide containing amino groups

Graphite oxide silylated by 3-aminopropylmethyldiethoxysilane was used an adsorbent of formaldehyde from gas phase at low concentration. The amount of formaldehyde adsorbed on this adsorbent was much higher than that on activated carbon, even when water molecules are preadsorbed. The utility of the amino groups seemed to be higher for the sample with lower contents of organic component between the graphite oxide layers and larger interlayer spacings.     

Formation of single-walled carbon nanotube thin films enriched with semiconducting nanotubes and their application in photoelectrochemical devices

Single-walled carbon nanotube (SWCNT) thin films, containing a high-density of semiconducting nanotubes, were obtained by a gel-centrifugation method. The agarose gel concentration and centrifugation force were optimized to achieve high semiconducting and metallic nanotube separation efficiency at 0.1 wt% agarose gel and 18,000g. The thickness of SWCNT films can be precisely controlled from 65 to 260 nm with adjustable transparency. These SWCNT films were applied in photoelectrochemical devices. Photocurrents generated by semiconducting SWCNT enriched films are 15-35% higher than those by unsorted SWCNT films. This is because of reducing exciton recombination channels as a result of the removal of metallic nanotubes. Thinner films generate higher photocurrents because charge carriers have less chances going in metallic nanotubes for recombination, before they can reach electrodes. Developing more scalable and selective methods for high purity semiconducting SWCNTs is important to further improve the photocurrent generation efficiency by using SWCNT-based photoelectrochemical devices.     

Time-resolved conformational analysis of poly(ethylene oxide) during the hydrogelling process

We investigated a drastic conformation change in a poly(ethylene oxide) (PEO) chain during the hydrogelation process using infrared (IR) spectroscopy and quantum chemical calculations (QCCs). Time-resolved in situ IR spectra of the hydrogelling process of a semi-crystalline PEO solid were measured using a flow-through cell. It was found from the time-resolved IR study that gauche conformations around the C-C bonds in the crystalline phase PEO chain maintain their conformations even after hydrogelation, while at least half of the trans conformations around the C-O bonds change into gauche conformations upon hydrogelling. With regard to the phenomena of these conformation changes after contacting water, the destruction and hydrogelation of the crystalline phase around the C-C bonds of the hydrophobic moiety occur prior to changes around the C-O bonds of the hydrophilic moiety. In addition, our QCC confirmed that the stable hydration structure of bridging water, wherein the two hydroxyl groups in a water molecule donate hydrogen bonds to every other ether oxygen atoms in the PEO chain.     

Metal adhesive properties of polyamides having the 2,3‐bis(1,4‐phenylene)quinoxalinediyl structure

Polyamides were synthesized by interfacial polycondensation of 2,3‐bis(4‐chloroformylphenyl)quinoxaline (BCFPQ) and several aliphatic diamines using a phase transfer catalyst, and their adhesive property for stainless steel was investigated. The inherent viscosity of the obtained polyamides ranged from 0.37 to 1.24 dL g⁻¹. The glass transition temperatures of the polyamides ranged between 154 and 201°C, and their thermal decomposition temperatures were above 450°C. The polyamides were soluble in several organic solvents, including m‐cresol, N‐methyl‐2‐pyrrolidone (NMP), and formic acid. The adhesive property for stainless steel was examined by a standard tensile test. One member of the series, polyamide P8, derived from BCFPQ and 1,8‐octanediamine, displayed high tensile strength with values of 232 kgf cm⁻² at 20°C, 173 kgf cm⁻² at 120°C, and 137 kgf cm⁻² at 180°C. Thus, the tensile strength of P8 decreased at 180°C, but the decrease was much smaller than that of an epoxy resin in wide use as a metal adhesive. Heat distortion temperature, measured by thermal mechanical analysis, of P8 was 191°C. This suggested that P8 possessed high thermal resistance in metal adhesives. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 1366–1370, 1999     

Control of the microparticle position in the channel based on dielectrophoresis

We report here the control of the microparticles position within fluid flow based on its size by using dielectrophoresis (DEP) with a microelectrode array consisted of rectangular features with the different size of width and gap. 3 μm- and 10 μm-diameter particles were introduced into the channel with 300 μm height at 30 μl/min. An AC electric field (20 V peak–peak and 2 MHz) was then applied to microelectrode arrays to form dielectrophoretic fluid cage, resulting in a formation of flow paths with low electric fields on the arrays. The microparticles separately flow in line streams along the paths formed between the rectangular features of the arrays, the 3 μm-diameter particles mainly flow through the narrow path and 10 μm-diameter particles through the wide path. These results indicated that positions of two types of microparticles in the fluidic channel were easily separated and controlled using the n-DEP.     

Rapid fabrication of nanoparticles array on polycarbonate membrane based on positive dielectrophoresis

We report here a rapid formation of island arrays with nanoparticles on and within polycarbonate (PC) membrane based on positive dielectrophoresis (p-DEP). For the fabrication of the patterning device, PC membranes with 10 μm thickness and 100, 200 or 400 nm pore size were sandwiched by an upper bare ITO substrate and a lower disk array ITO electrode which was defined by insulation layer of negative photoresist. A suspension of 190 nm diameter polymethylmethacrylate (PMMA) particles containing rhodamine 6G (R6G) fluorescent molecules was introduced into the device between the upper ITO and the PC membrane. AC electric signal (typically 20 Vpp, 70 kHz) was then applied to the ITO, resulting in the formation of island patterns with high electric fields gradient regions on and in the PC membrane. Particles patterns with island shape were assembled on membrane within 1 s after applying AC electric field. The electrodes can be used repeatedly as the template of subsequent patterning. Although, particles islands were only formed on the PC membrane with 100 and 200 nm diameter pores, the particles penetrated the membrane with 400 nm pores to form patterns on the back surface. Since the strong electric fields were formed at the edges of disks, particles on the back surface were the projection of the disk array of ITO to form ring shapes. The unique structure with particles was explained based on the simulation of electric field distribution. The present proposal offers a procedure to fabricate particle arrays with extremely simple, rapid and highly reproducible manner.