Structural interpretation of plasma-polymerized propargyl alcohol

Vapor of propargyl alcohol under reduced pressure was glow-discharged for plasma polymerization by which hydrophilic polymer film could be deposited onto a solid substrate. The hydrophilic property was more enhanced with use of the same monomer containing water. An interpretation of chemical structures of the polymer molecules was therefore attempted to discover the reason of the hydrophilic property. The polymer materials were subjected to IR spectroscopy, ¹³C-NMR and ¹H-NMR spectroscopies, elemental analysis, number average molecular weight determination, mass spectrometry, and other wet chemical analysis for . The IR spectra of the polymers showed the presence of OH, C?O, and C?C groups with a disappearance of C?C group of the monomer. It was also found that the molecular formula of a solvent extract of the polymer derived from the plain monomer was C₂₆H₃₆O₉ ≒ 490, involving four hydroxyl, one carbonyl, and two to three olefinic unsaturation groups within a unit molecule. On the other hand, the polymer from 60% water-containing monomer showed its molecular formula as C₄₄H₆₆O₁₈ ≒ 890, containing seven to eight hydroxyl, two carbonyl, and one to two olefinic unsaturation groups. This information was used to establish the symbolic chemical structures of the polymer molecules. It has been found that both polymers were not as much crosslinked as other plasma polymers because of having side chains with fewer branching. The oxygen atoms were retained in the polymer not only as the forms of OH and C?O but also as a member of the principal frame of the polymers.     

Wind tunnel study on wind and turbulence intensity profiles in wind turbine wake

In recent years, there has been a rapid development of the wind farms in Japan. It becomes very important to investigate the wind turbine arrangement in wind farm, in order that the wake of one wind turbine does not to interfere with the flow in other wind turbines. In such a case, in order to achieve the highest possible efficiency from the wind, and to install as many as possible wind turbines within a limited area, it becomes a necessity to study the mutual interference of the wake developed by wind turbines. However, there is no report related to the effect of the turbulence intensity of the external flow on the wake behind a wind turbine generated in the wind tunnel. In this paper, the measurement results of the averaged wind profile and turbulence intensity profile in the wake in the wind tunnel are shown when the turbulence intensity of the external wind was changed. The wind tunnel experiment is performed with 500mm-diameter two-bladed horizontal axis wind turbine and the wind velocity in wake is measured by an I-type hot wire probe. As a result, it is clarified that high turbulence intensities enable to the entrainment of the main flow and the wake and to recover quickly the velocity in the wake.     

Nanostructured Fe-Pd thin films for thermoelastic shape memory alloys—electrochemical preparation and characterization

Nanostructured Fe-Pd thin films with about 30 at.% Pd have been successfully synthesized on the substrates of Pt buffer layer/Cr seed layer/Si by an electrodeposition process from a plating bath containing ammonium tartrate, citric acid and ammonia solution as complexing agents. Results clearly show that the as-deposited films with body-centered cubic structure were transformed into face-centered cubic structure by heating at 900 °C for 45 min followed by quenching into iced water. The in situ X-ray diffraction analysis results indicate that the quenched film with 29.8 at.% Pd undergoes a reversible thermoelastic austenite-to-martensite transformation with a narrow temperature hysteresis and a martensite transformation temperature of about −30 °C. The present study demonstrates the effectiveness of electrodeposition for synthesizing nanostructured Fe-Pd thin films for the application of low-temperature-type thermoelastic shape memory alloys.     

混凝超滤工艺处理天津渤海湾海水

试验考核在线混凝超滤工艺预处理天津渤海湾海水的可行性,采用外压式中空纤维超滤膜,研究膜的最大膜通量,以及通过数据和理论公式分析得到该工艺的最佳化学强化清洗方式.试验分3阶段进行,每阶段采用不同膜通量和化学强化清洗方式.3个月试验结果表明:在跨膜压差≤75 kPa时能保证系统稳定运行的最大膜通量为54.2 L/(m2·h);最佳化学强化清洗方式为:气水擦洗,pH=2的H2SO4和质量分数120×10-6的NaClO相继连续清洗,气水擦洗,质量分数0.15×10-6亚硫酸氢纳浸泡,气水擦洗,清洗频率为1次/d;同时清洗效果表明,H2SO4和NaClO清洗对膜污染控制有不同的作用,H2SO4清洗有利于去除该工艺的不可逆污染物,NaClO清洗有利于减缓膜污染;试验产水满足反渗透进水要求,产水中未监测到藻类,产水浊度在0.06～0.1 NTU之间,SDI15<3,CODMn去除率为26%～45%.     

Potentiometric immunosensor using artificial antibody based on molecularly imprinted polymers

A potentiometric artificial immunosensor based on a molecularly imprinted polymer was prepared as a detecting element in micro total analysis systems with the intent of providing easy clinical analysis. As the structure and transducing mechanism of this sensor are very simple, construction of a single microsensor should be quite easy. Multimicrosensor arrays applicable to several kinds of analytes will be attainable by both changing the template molecule to be imprinted and reducing the sensor size. The response characteristics of this sensor were evaluated by measuring the response potential to serotonin, which was used as a model material. The obtained sensor was highly responsive to serotonin in water but not to tryptamine, acetaminophen, or procainamide. This phenomenon confirms that the sensor recognizes serotonin and that it functions as a specific artificial immunosensor. Quick measurement is possible because the response time, defined as the time required to achieve 95% of the magnitude of the equilibrated signal, correspond to approximately 12 s. The sensor's determination and detection limits were found to be 1 mumol/L and 100 pmol/L, respectively. These results suggest that our strategy can be applied to construction of a potentiometric artificial immunosensor.     

Free-standing,roll-able,and transparent silicone polymer film prepared by using nanoparticles as cross-linking agents

A free-standing, roll-able, and transparent silicone-based polymer film with a tensile modulus of ca. 7.8 MPa and strain at the break point of 0.76% was successfully prepared by reaction between a reactive silicone oligomer with methyl- and methoxy-side groups and hydrophilic SiO₂ nanoparticles. First, SiO₂ nanoparticles were grafted with silicone chains by a controlled wet chemical sol–gel-type reaction with the reactive oligomers. The solvent of the resulting solution was evaporated to form a viscous suspension, casted into a film, and finally heat-treated at 100 °C and 150 °C. A hydrolysis and condensation reaction among silicone-grafted SiO₂ nanoparticles and free silicone oligomers in the final heat treatment resulted to produce free-standing, roll-able, and transparent silicone-based polymer film. The fact that the silicone film cannot be synthesized without the presence of SiO₂ nanoparticles suggests that these nanoparticles act as cross-linking agents of silicone components providing the improved mechanical properties to the composite film. The rate-controlled mixing and heating of the SiO₂ aqueous/alcohol suspension and the silicone oligomer/alcohol solution was found to be the key step in the synthesis of the free-standing transparent film. While rapid addition/mixing resulted in a fragile and opaque film, a transparent material was achieved when those solutions were slowly mixed. The effect of the synthesis process on the macroscopic and microscopic properties of the prepared films is discussed along with their formation mechanism.     

Elution of sodium caseinate from agar-based gel matrixes in simulated gastric fluids

Elution of sodium caseinate from agar/psyllium composite gels was investigated in simulated gastric fluids to determine predominant mechanical parameters of gels for the elution kinetics and to predict the kinetics using the parameters. When the concentration of agar was fixed at 0.5% in the composite gels, elastic moduli determined by creep tests decreased with increasing concentration of psyllium, while viscosities increased. Compression load upon syringing through an enteral tube increased with increasing concentration of psyllium, whereas the surface-volume diameter d_3,2 of gel particles after syringing decreased. The elution kinetics of sodium caseinate from cylindrical gels was described using two different diffusion coefficients; D₁ and D₂ (D₁ > D₂) and the diameter of gels. Both diffusion coefficients decreased with increasing concentration of psyllium, resulting in 1.9 × 10⁻⁶ (for D₁) and 6.7 × 10⁻⁸ (for D₂) cm²/min by 1.5% addition, which corresponded to approx. 30% and 45% of the control (i.e., 0% psyllium), respectively. The fraction ratio of sodium caseinate having D₁ was not sensitive to psyllium concentration; approx. 80%–85% in the concentration range tested. D₁ was inversely proportional to viscosities determined by creep tests, particularly one from the Voigt body η₁ in the 4-element mechanical model. When cube gels were divided into smaller ones without changing the total volume, elution rates were inversely proportional to the cube length, where the diffusion coefficients did not change. The elution kinetics of sodium caseinate from the gel matrixes was anticipated using η₁ of gels before syringing and d_3,2 of gel particles after syringing when the usage of gels for percutaneous endoscopic gastrostomy is assumed.