Emission of Particulate Matter 2.5 (PM2.5) from Sewage Sludge Incinerators in Japan

Because fine particulate matter ≤2.5 µm in diameter (PM2.5) causes health problems, PM2.5 emissions are of concern. However, little research on stationary sources has been conducted. To determine the concentration and filtration behavior of PM2.5, dust was collected from five fluid-bed sewage sludge incinerators (SSIs) sorted by particle size using cascade impactors. The average PM2.5 concentration was 0.00014–4.8 mg/Nm³. The total estimated amount of PM2.5 emissions from the SSIs for all plants in Japan was 0.96–8.9 tons/year. Since the SSIs with dry Electrostatic Precipitators (EP) contributed 75–99% of the total emissions, replacing dry EPs with bag filters would significantly reduce the PM2.5 emissions from SSI.     

Kinetically Stable Bicelles with Dilution Tolerance,Size Tunability,and Thermoresponsiveness for Drug Delivery Applications

Mixtures of a phospholipid (1,2‐dipalmitoyl‐sn‐glycero‐3‐phosphatidylcholine, DPPC) and a sodium‐cholate‐derived surfactant (SC‐C₅) at room temperature formed phospholipid bilayer fragments that were edge‐stabilized by SC‐C₅: so‐called “bicelles”. Because the bilayer melting point of DPPC (41 °C) is above room temperature and because SC‐C₅ has an exceptionally low critical micelle concentration (<0.5 mm ), the bicelles are kinetically frozen at room temperature. Consequently, they exist even when the mixture is diluted to a concentration of 0.04 wt %. In addition, the lateral size of the bicelles can be fine‐tuned by altering the molar ratio of DPPC to SC‐C₅. On heating to ≈37 °C, the bicelles transformed into micelles composed of DPPC and SC‐C₅. By taking advantage of the dilution tolerance, size tunability, and thermoresponsiveness, we demonstrated in vitro drug delivery based on use of the bicelles as carriers, which suggests their potential utility in transdermal drug delivery.     

Curing of epoxy resin by ultrafine silica modified by grafting of hyperbranched polyamidoamine using dendrimer synthesis methodology

Hyperbranched polyamidoamine–grafted silica was prepared according to dendrimer synthesis methodology. The modified silica was dispersed uniformly in epoxy resin, and the curing of epoxy resin proceeded successfully by heating in the presence of the modified silica; the gel fraction of the epoxy resin cured by the hyperbranched polyamidoamine–grafted silica (grafting = 80.2%) reached 77% at 170°C after 48 h. The gel fraction increased with increasing terminal amino group content of the hyperbranched polyamidoamine–grafted silica. In addition, the curing ability of the silica increased by complexation of the terminal amino groups of the grafted polyamidoamine with boron trifluoride. The modulus of elasticity of the curing materials obtained using the modified silica as a curing agent was lower than that using conventional a curing agent such as ethylenediamine in the presence of untreated silica. On the other hand, the heat resistance of the curing product using the modified silica was superior to that using ethylenediamine, but no difference in glass‐transition temperature was observed. It is expected that hyperbranched polyamidoamine grafted‐silica is incorporated uniformly with chemical bonds in the matrix of the epoxy resin. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 573–579, 2001     

Improvement of lysozyme recovery method from the precipitate of protein-anionic surfactant complexes

A new protein separation process using a surfactant and a polar organic solvent consists of a precipitation step and a recovery step. In the precipitation step, a protein-surfactant complex is precipitated from an aqueous solution, when an ionic surfactant, sodium di(2-ethylhexyl) sulfosuccinate (AOT), is added to an aqueous solution, including protein (lysozyme). In the recovery step, the precipitate is dissolved in a polar organic solvent, such as acetone, and the protein is recovered as precipitates when a very small amount of salt solution was added to remove surfactants from the protein-surfactant complex. However, the details of the protein recovery step from precipitate have not been studied yet. In this study, the improvement of the protein recovery step was examined from the viewpoint of a recovery ratio of protein and a remaining ratio of surfactant. The optimum NaCl concentration in the feed for the protein recovery was in the range of 0.05–0.2 kmol/m³. As the NaCl concentration in the feed increased to more than 0.2 kmol/m³, the precipitation ratio decreased due to the electrostatic screening effect of NaCl. It was found that the addition of a very small amount of NaCl solution to acetone was unnecessary when NaCl was included in the feed lysozyme solution. On the other hand, as the NaCl concentration decreased to less than 0.05 kmol/m³, the precipitation ratio was decreased due to the low re-precipitation of protein by the addition of a small amount of NaCl solution in acetone. In the case of the feed containing no salt, the desired NaCl concentration added to acetone was in the range above 0.2 kmol/m³. In addition, the most suitable volume ratio of acetone to feed was found to be 0.2.     

Characteristics and Reactivity of Lignin in Acacia and Eucalyptus Woods

The chemical characteristics of lignin, including the Klason lignin content, acid-soluble lignin content, proportion of the aromatic ring types [syringyl ratio = syringyl/(syringyl + guaiacyl)], and proportion of the diastereomeric forms for the β-O-4 structure [erythro ratio = erythro/(erythro + threo)], and pulpability were investigated for 28 wood samples belonging to the genera Acacia and Eucalyptus. Although the lignin characteristics of these 28 woods varied widely, the chemical characteristics of the two genera could be categorized in two clearly distinguished groups on the basis of the syringyl ratio. Clear negative correlations were observed between both the syringyl and erythro ratios and the total lignin content (sum of the Klason and acid-soluble lignin contents) within each genus. In addition, the syringyl ratio correlated positively with the erythro ratio and acid-soluble lignin content, regardless of the genus. The existence of a clear, high correlation between the syringyl and erythro ratios supports the hypothesis that the aromatic ring type (syringyl ratio) is a decisive factor for controlling the diastereomeric forms of the β-O-4 structure (erythro ratio). Each of the wood samples was also subjected to Kraft pulping, and it was demonstrated that the woods with higher syringyl ratios were easier to delignify. This tendency is reasonably attributed to the high reactivity of the erythro-rich and syringyl-rich β-O-4 structures, and the low lignin content of these syringyl-rich woods.     

Synthesis of polyamides from sugar derived d-glucaric acid and xylylenediamines

d -Glucaric acid (GA) is the one of aldaric acids and is an important bio-based building block for polymers. In this study, poly(m-xylylene-acetyl glucaramide) and poly(p-xylylene-acetyl glucaramide) were synthesized from GA acetate and two kind of aromatic diamines by solution polymerization. The chemical structures of the polyamides were analyzed by nuclear magnetic resonance spectroscopy. The weight-average molecular weights ranged from 3.3 × 10³ to 1.15 × 10⁴ with a polydispersity of 1.6–1.9, depending on monomer ratio or monomer concentration in solution. The 10% decomposition temperature of the polymers was about 210 °C. Differential scanning calorimetry revealed that the polyamides exhibited no peaks attributed to crystallization or melting point, which indicated that the polyamides were amorphous. No crystalline pattern was observed in the X-ray diffractograms, supporting this result. Polarized optical microscopy observation revealed that the polyamides exhibited melting-like behavior at above 150 °C, which was attributed to glass-transition behavior. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47255.     

On the onset of fracture as a silicon-based polymer converts into the ceramic phase

Silicon-based polymers evolve into refractory ceramics when heated gradually up to ~1000°C. The conversion is accompanied by the loss of gaseous species, and by a two-fold increase in density. The shrinkage can produce microcracks if the heating rate is too high, or if the specimen is too thick. This communication builds on earlier work whereby the measurement of gas evolution, and its relationship with viscous flow, are related to the onset of fracture in disk-shaped green (polymer) samples. The onset is determined as a function of the thickness of the disks, and of the heating rate. The results are presented in the form of a processing map. The overlay with gas evolution, and strain-rate measurements, suggest that fracture initiates with the release of hydrogen and methane, starting at temperatures near 750°C.     

Low-Temperature Magnetotransport and Magnetic Properties of Cobalt-Doped Amorphous Carbon Thin Films

采用磁控共溅射方法在n型Si(100)基片上制备了一系列具有不同Co含量(x,at％)的Co掺杂非晶C颗粒薄膜,溅射温度为室温.研究了Co-C颗粒薄膜的微结构,磁输运特性及磁性能.通过优化Co含量,在低温下发现了较大的负磁电阻(MR).温度为2K、磁场为90×79.6 kA.ml时,Co含量为6.4 at％的Co-C薄膜的负磁电阻值最大,达到27.6％.随着Co含量从6.4 at％增加至16.4 at％,MR 值从27.6％逐渐减小至2.2％.电阻率ρ随温度T的变化曲线显示了线性的lnρ-T1/2关系,说明样品中电子传导遵循隧穿输运机制.     

Porous Titania Ceramic Prepared by Mimicking Silicified Wood

A porous titania ceramic with a woodlike microstructure that was analogous to silicified wood was prepared. The production of "titanified wood" was performed using the following process: (i) introduction of titanium tetraisopropoxide into wood materials via vacuum infiltration, (ii) hydrolysis of the titanium tetraisopropoxide in the cell structure to form a titania gel, and (iii) firing at a temperature of 600°–1400°C in air. The resulting titania ceramic had the same external and internal forms of the original wood.     

Molecular simulation for adsorption of chlorinated hydrocarbon in zeolites

Equilibrium and isosteric heat of adsorption for the system of chloroform and USY-type zeolite were studied. The USY-type zeolite (PQ Co., SiO₂/Al₂O₃=70) was used both as a pure crystalline powder and as granulated particles with binder. Chloroform was reagent grade. The adsorption equilibria were measured using a gravimetric method and were expressed as isotherms. A chromatographic method (i.e. pulse response of chloroform through the USY column with helium carrier) was used to get the initial slope of the isotherms. In the simulation, the GCMC method was used to calculate amounts adsorbed for various conditions. FF parameters were confidently applied. And modified structure model was effective for simulation. This paper was presented at The 5th International Symposium on Separation Technology-Korea and Japan held at Seoul between August 19 and 21, 1999.