A Practical Model for the Interactions Between Hydrating Portland Cements and Poly-β-Naphthalene Sulfonate Condensate Superplasticizers

The performance of poly-β-naphthalene sulfonate condensate superplasticizer (BNS) as a dispersant for cement in concrete is affected severely by slight differences in the characteristics of the cement. In order to be able to predict these effects, a model for estimating the fluidity of cement paste containing BNS is proposed. This model is based on an assumption that the fluidity of cement paste is proportional to the BNS adsorption amount per surface area of hydrated cement (Ad/Hy). BNS is known to show two types of sorption on hydrated cement: one is the bulk absorption into initial hydrates and the other one is the superficial adsorption onto hydrates. Only the superficially adsorbed BNS is expected to work as a dispersant. By assuming a competitive Langmuir-type adsorption on hydrates between BNS and SO₄²⁻, a simple method to estimate Ad/Hy is developed, with the concentrations of BNS and SO₄²⁻ as the only two independent parameters. The resulting estimates of Ad/Hy show a good correlation with paste flow and its change with elapsed time for a broad range of cements. The SO₄²⁻ concentration in the aqueous phase of the cement paste just after the beginning of the mixing is known to affect the performance of BNS as a dispersant. By using the proposed model to discriminate between the superficial adsorption and bulk absorption of BNS, this phenomenon is explained quantitatively.     

Anatase-Type TiO2 and ZrO2-Doped TiO2 Directly Formed from Titanium(III) Sulfate Solution by Thermal Hydrolysis: Effect of the Presence of Ammonium Peroxodisulfate on their Formation and Properties

Anatase-type TiO₂ powder containing sulfur with absorption in the visible region was directly formed as particles with crystallite in the range 15–88 nm by thermal hydrolysis of titanium(III) sulfate (Ti₂(SO₄)₃) solution at 100°–240°C. Because of the presence of ammonium peroxodisulfate ((NH₄)₂S₂O₈), the yield of anatase-type TiO₂ from Ti₂(SO₄)₃ solution was accelerated, and anatase with fine crystallite was formed. Anatase-type TiO₂ doped with ZrO₂ up to 9.8 mol% was directly precipitated as nanometer-sized particles from the acidic precursor solutions of Ti₂(SO₄)₃ and zirconium sulfate in the presence and the absence of (NH₄)₂S₂O₈ by simultaneous hydrolysis under hydrothermal conditions at 200°C. By doping ZrO₂ into TiO₂ and with increasing ZrO₂ content, the crystallite size of anatase was decreased, and the anatase-to-rutile phase transformation was retarded as much as 200°C. The anatase-type structure of ZrO₂-doped TiO₂ was maintained after heating at 1000°C for 1 h. The favorable effect of doping ZrO₂ to anatase-type TiO₂ on the photocatalytic activity was observed.     

Feasible method,utilizing density changes,for estimating in situ dynamic strength and deformation properties of sand samples

Laboratory tests and design reliability are directly controlled by sample quality. The frozen sampling (FS) method is useful for dynamic strength and deformation tests of undisturbed clean sand. However, it is very expensive and requires considerable equipment. The sample quality of Toyoura sands obtained from 48 mm and 75 mm samplers are scrutinized based on void ratio, dynamic strength and deformation properties through model and cyclic undrained triaxial tests. A conventional method for estimating in-situ dynamic strength and deformation properties of sand samples utilizing density changes is examined and the applicability of the proposed method is discussed for the samples obtained from Niigata sand deposits.The main conclusions obtained from this study are summarized as follows:(1) A conventional method for estimating in-situ void ratio (e₀), D_r, stress ratio (R_L20) in a 20 cyclic time frame and the initial modulus of rigidity (G₀) of sand samples utilizing density changes is proposed.(2) The in-situ R_L20 and G₀ estimated from the proposed method for sand samples from tube samplers were similar to those of frozen sampling and the in-situ modulus of initial rigidity was calculated from the secondary wave velocity for Niigata sand deposits.Therefore, dynamic strength and deformation properties changes, caused by sampling, can be modified appropriately to an in-situ condition by this proposed method.     

Surface activity of aqueous solutions of cellulose acetate with low degree of substitution

Surface activity of aqueous solutions of cellulose acetate (CA) with total degree of substitution (〈F〉) ranging from 0.58 to 0.80 was examined. Critical micelle concentration (CMC) of the aqueous CA solutions, determined from the polymer concentration dependence of surface tension (γ), is unequivocally determined by 〈F〉, and an increase in 〈F〉 of CA brings about a lowering of the CMC. From light scattering measurements on aqueous solutions of CA with 〈F〉 = 0.8 at 20°C, it was revealed that in the vicinity of the CMC the micelles in the solution consist of c. four CA molecules, which is very close to the value obtained by analysing the data obtained from the mass action model. The surface tension of aqueous solutions of CA (〈F〉 = 0.8) in the polymer concentration range above the CMC was c. 0.74 times that of pure water over the temperature range 0–80°C.     

Mid-infrared spectroscopic measurement of ionic dissociative materials in the metabolic pathway

We determine the pH dependency of the mid-infrared spectra in aqueous solution of the organic dissociative materials in the metabolic pathway: saccharide phosphates (G6P, F6P), adenosine, and its phosphates (ATP, ADP, AMP). The series of molar absorbance spectra for these reagents were obtained in a pH range of about 2 to 11 with a Fourier transform infrared (FT-IR) spectrometer equipped with a horizontal diamond attenuated total reflection (ATR) sampling accessory. We also provide a method of infrared spectral extraction of ionic dissociative materials by performing a linear least-square fitting utilizing the formulas of ionic dissociation equilibrium shift, and we obtain the infrared spectrum of each ionic species of the dissociative materials: G6P-, G6P2-; F6P-, F6P2-; ATP2-, ATP3-, ATP4-; ADP-, ADP2-, ADP3-; AMP, AMP-, AMP2-; and adenosine+, adenosine0. The infrared spectral structure of each ionic species of the dissociative materials in the metabolic pathway are discussed. Additionally, the possibility for a quantification system of the concentrations of the organic dissociative materials in varying pH is suggested.     

Study on chemical structures of poly (tetrafluoroethylene-co-perfluoroalkylvinylether) by soft-EB irradiation in solid and molten state

Poly (tetrafluoroethylene-co-perfluoroalkylvinylether) (PFA) was irradiated by soft electron beam (soft-EB) under nitrogen gas atmosphere in solid-state and its molten state, respectively. The changes of thermal property and chemical structures of irradiated PFA in solid-state and molten state were studied by differential scanning calorimetric analysis (DSC) and solid-state ¹⁹F magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy. By DSC analysis, the melting temperature shifted to lower temperatures, and crystallinity decreased with increasing soft-EB dose. By solid-state ¹⁹F MAS NMR spectroscopy, the new signals was observed and the detected new signals in irradiated PFA at 315 °C and at 30 °C were due to the tertiary carbon group with branching site (Y-type crosslinking site), perfluoro-propylene site and chain end methylene groups, respectively.Moreover, the molar ratio of perfluoroalkylvinylether (FAVE) structure to -CF₂- units decreased with increasing dose.     

Present status of beryllides for fusion and industrial applications in Japan

Beryllides have remarkable characteristics besides their low density, such as high radiation resistance, high chemical stability, low hydrogen isotope retention and good high temperature mechanical strength especially for fusion applications. In order to have a practical usage for industrial applications, it is important to compile a set of quantitative data on such properties. It is also important to develop fabrication and processing paths to assure the processing of inherently brittle beryllides.The characterization and manufacturing technologies development have been carried out mainly on the Be₁₂Ti interemetallic compounds at the Be-rich side of the Be-Ti binary system. In the present paper, up-dated results on several properties are described for the compound fabricated by hot isostatic pressing (HIP) and ingot metallurgy. Mechanical properties of the compounds having a duplex microstructure with neighboring phases are evaluated by compressive tests from room temperature to 1273 K. Radiation damage of the compound is preliminary studied by charged particle irradiation. Oxidation in air and the interaction with water vapor are evaluated. Thermal desorption of the deuterium is examined by using transmission electron microscopy (TEM) and thermal desorption spectrometry (TDS). Through these evaluations it seems that Be₁₂Ti is superior as neutron multiplier with respect to pure Be metal.     

Critical Heat Flux of Boiling Heat Transfer in a Moderate Narrow Space

INTanDUCTI0NBoilingheattransferandcriticalheatflux(CHF)inaconfinednarrowspacehavebeenstudiedexperi-melltallybyanumberofinvestigatorsinthepastfewdecades.However,thereisnoanypopularlyacceptedmodelintheheattransferinnarrowspaceboiling,althoughsomepopularknowledgeabouttheboilingheattransferinthenarrowspacehavebeenacceptedbymanyresearchers.Theknowledgecanbecon-cludedasthatthenucleateboilingheattransferisenhancedatlowheatfluxregionanddeterioratedathighheatfiuxregi0nespeciallyatCHF.Theenhanceme…     

Input power factor control of three‐phase to three‐phase matrix converters

This paper presents input power factor control of three‐phase to three‐phase matrix converters. The authors propose three kinds of switching patterns for the matrix converters that can realize an arbitrary input‐power‐factor angle between 0 and 2π and reduce the number of commutations in all three phases to four during the control period. Also, the control range of the output voltage reference in the proposed control scheme is derived. The improvement of the input power factor by using the proposed control algorithm has been verified by experiments. © 2011 Wiley Periodicals, Inc. Electr Eng Jpn, 178(3): 42–52, 2012; Published online in Wiley Online Library ( wileyonlinelibrary.com ). DOI 10.1002/eej.21199