The Oxidation of Manganese and Disinfection By Ozonation in Water Purification Processing

The surface water of a river has been used as the raw water by the Waterworks Bureau of Osaka City. At present, the manganese contained in the raw water is oxidized by breakpoint chlorination and all oxides are removed by coagulation, sedimentation followed by rapid sand filtration, with chlorine being used as the final disinfectant.

Prechlorination was not conducted in the ongoing pilotplant experiment of an advanced water purification process with ozone and granular activated carbon. It is necessary, therefore, to oxidize manganese by the oxidative effect of ozone instead of prechlorination.

It is important for the treatment of manganese to adjust the ozone dosage because manganese is oxidized up to the soluble septavalent state by the surplus ozone. Since ozone does not continue to exist for very long in water, though its disinfecting power is high, final disinfection by chlorine is required.     

Molecular dynamic simulation of heterogeneity and chemical states of fluorine in amorphous alkaline earth silicate systems

Chemical states of fluorine in fluorosilicate glasses in the system MF₂-MO-SiO₂ (M = Ca, Sr and Ba; SiO₂ content < 60 mol%) have been investigated by molecular dynamic (MD) simulations with a perfect ionic two-body potential. Comparison of the results with those derived by X-ray photoelectron spectra of the actual glasses demonstrates that MD simulations reproduce well the bonding states of fluorine in the systems as well as the formation of M-F clusters. The MD generated structure of imaginary glasses, or glasses not obtained by the conventional melt-quench technique, with 70 mol% SiO₂ indicates that an acidic environment induces a greater amount of F---Si bonds. Their M-F pair correlation functions plotted against normalized M-F distances suggest that relative ion positions in the clusters are very similar.     

Superconducting critical current in MoN

Journal of Materials Science Letters -     

Facile one-step route to polyaniline–silver nanocomposite particles and their application as a colored particulate emulsifier

Polyaniline–silver nanocomposites were synthesized in the form of colloidal particles by the facile one-step aqueous chemical oxidative dispersion polymerization of aniline using silver nitrate as an oxidant and poly(vinyl alcohol) as a colloidal stabilizer. Aniline monomer was oxidized by silver ions, yielding polyaniline and elemental Ag simultaneously. The synthesized nanocomposite particles were colloidally stable over 2 years and transmission electron microscopy studies indicated the production of spherical, plate and rod-shaped polyaniline–silver nanocomposite particles with a silver core–polyaniline shell morphology. The conductivity of a pressed pellet of the nanocomposite particles using the conventional four-point probe technique was 1.4 × 10^?2 S/cm at 25 °C. The nanocomposite particles behaved as a ‘colored’ particulate emulsifier for the stabilization of transparent oil-in-water emulsions.     

Mechanical properties of silane‐treated,silica‐particle‐filled polyisoprene rubber composites: Effects of the loading amount and alkoxy group numbers of a silane coupling agent containing mercapto groups

The surface treatment of spherical silica particles with a silane coupling agent with mercapto groups was carried out. The treated silica particles were incorporated within polyisoprene and then vulcanized. The effects of the loading amount and alkoxy group number of silane on the stress–strain curve of the filled composite were investigated. For this purpose, silanes with dialkoxy and trialkoxy structures were used. The loading amount of silane on the silica surface was varied from 1 to 8 times the amount required for monolayer coverage. The stress at the same strain increased with the silane treatment, and it was higher in the dialkoxy structure than in the trialkoxy structure above 300% strain. There was no significant influence of the loading amount on the stress for the trialkoxy silane structure. However, the stress was influenced by the loading amount, and the maximum stress was observed at 4 times the silane amount required for monolayer coverage for the dialkoxy structure. The stress had a good relationship with the crosslinking density of silica‐filled polyisoprene rubber (measured with a swelling test). The reinforcement effect by the silane treatment of silica was found to be affected strongly both by the entanglement of the silane chain and polyisoprene rubber matrix and by the crosslinking reaction between the mercapto group of silane and polyisoprene rubber in the interfacial region. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Structure of silane layer formed on silica particle surfaces by treatment with silane coupling agents having various functional groups

The surface treatment of spherical silica particles with silane coupling agents having various organic functional groups was conducted and the effect of the alkoxy group number on the molecular flexibility of the silane chain with multilayer coverage was investigated using ¹H-pulse nuclear magnetic resonance spectroscopy. The silica particles were treated with 2-propanol solution and heated at 120?°C for 24?h after solvent evaporation to accelerate the polycondensation reaction of silanol groups. For multilayer coverage, flexible linear chain and rigid network structures were expected to form on the surface from the di- and trialkoxy structures, respectively. However, the rigid network structure was formed from both the di- and trialkoxy structures with glycidoxy, amino, and methacryloxy functional silanes. Ring opening of the epoxy group occurred, followed by reaction to form the network structure, even with the dialkoxy structure of the glycidoxy functionality. Ring opening of the epoxy group could be reduced by pH adjustment of the treatment solution and the linear chain structure was formed from the dialkoxy structure. In the case of amino and methacryloxy functional groups, hydrogen bonds were formed between the amino or methacryloxy groups and the silanol groups on the silica surface or silane molecules.     

Sawtooth-shaped stringiness with front frame formation for polyacrylic pressure-sensitive adhesives with two different molecular structures

The formation of sawtooth-shaped stringiness during 90° peeling was investigated using crosslinked poly(n-butyl acrylate–acrylic acid) and poly(2-ethylhexyl acrylate–acrylic acid) random copolymers with an acrylic acid content of 5 wt.% and different crosslinking degrees as pressure-sensitive adhesives (PSAs). The gel fraction was measured by toluene extraction of PSA, and it increased with crosslinker content for both systems. The observed stringiness was sawtooth-shaped, but there were three different types; both the typical sawtooth shape and the frame formed at the front tip with interfacial failure, and the sawtooth shape formed with cohesive failure. The change in the stringiness shape was affected strongly by the gel fraction of PSA. The peel rate under constant peel load was measured and revealed that the peel rate was lowest upon formation of the front frame type. A good relation was found between peel rate and peel strength, with a greater peel strength upon formation of the front frame type. The concentrated stress at the peeling tip is released by progress of peeling and deformation of the adhesive layer (stringiness) for no frame type. On the other hand, the sufficient interfacial adhesion delays the progress of peeling, and the applied larger stress causes cavitation in the PSA layer for front frame type. The formed cavity grows and the front frame type formed as a result. That is, internal deformation occurred preferentially over peeling. In order to improve the peel strength, the front frame type is the most useful stringiness shape.     

Influences of debonding rate and temperature on tack properties and peel behavior of polyacrylic block copolymer/tackifier system

The influences of debonding rate and temperature on the peel behavior of polyacrylic block copolymer/tackifier system were investigated. Poly(methyl methacrylate)-block-poly(n-butyl acrylate)-block-poly(methyl methacrylate) triblock copolymer (MAM) with hard block contents of 23 (MAM-23) and 16 wt.% (MAM-16) and a 1/1 blend with a diblock copolymer (MA) consisting of the same components (MAM-23/MA, total hard block content of 15 wt.%) were used as the base polymer. A special rosin ester was used as a tackifier at various contents in the block copolymer/tackifier system. The peeling process at the probe/adhesive interface during probe tack testing was observed using a high-speed microscope at 23 °C with debonding rate of 10 mm/s. Three different peeling mechanisms were observed. Type A, where peeling progressed linearly from the edge to the center of the probe without cavitation (MAM-23). Type B, where peeling progressed linearly from the edge to the center of the probe with cavitation (MAM-16). Type C, where cavitation occurred over the entire adhesive layer, and peeling initiation was delayed (MAM-23/MA). The peel behavior of MAM-23 changed from Type A to Type B with a decrease of the debonding rate (1 mm/s) or increase of the temperature (40 °C). In contrast, there was no change for MAM-16 and MAM-23/MA. Cavity formation in an adhesive layer restrains peeling; therefore, it is desirable for improvement of the adhesion strength. The tack properties increased with the tackifier content, and the formation of cavitation was less than that for the systems without the tackifier.     

Influence of diblock addition on tack in a polyacrylic triblock copolymer/tackifier system measured using a probe tack test

The influence of diblock copolymer addition on the tack properties of a polyacrylic triblock copolymer/tackifier system was investigated. For this purpose, poly(methyl methacrylate)‐block‐poly(n‐butyl acrylate)‐block‐poly(methyl methacrylate) triblock copolymer (MAM) and a 1/1 blend with a diblock copolymer consisting of the same components (MA) were used as base polymers, and a tackifier was added in amounts ranging from 10 to 30 wt %. The temperature dependence of tack was measured by a probe tack test. The tack of MAM/MA at room temperature was significantly higher than that of MAM, and the improvement of MAM/MA upon the addition of the tackifier was higher than that of MAM. The peeling process at the probe/adhesive interface during the probe tack test was observed using a high‐speed microscope. It was found that for MAM/MA, cavitation was caused in the entire adhesive layer, and peeling initiation was delayed by the absorption of strain energy due to deformation of the adhesive layer. In contrast, for MAM, peeling progressed linearly from the edge to the center of the probe. The greater flexibility of the soft block chain in the diblock copolymer resulted in improved interfacial adhesion. ¹H pulse nuclear magnetic resonance analysis showed that the addition of the tackifier improved the cohesive strength of the adhesive. Adhesion strength is affected by two factors: the development of interfacial adhesion and cohesive strength. In the MAM/MA/tackifier system, the presence of MA and the tackifier improved the interfacial adhesion and cohesive strength, respectively. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013