Effect of Composition on the Oxygen Tracer Diffusion in Transparent Yttrium Aluminium Garnet (YAG) Ceramics

The grain boundary structure and oxygen tracer diffusion in transparent yttrium aluminum garnet (YAG) ceramics varying from 2% excess of Y₂O₃ to 0.5% excess of Al₂O₃ were studied. The characterization of the specimens is as follows: (i) For the Y₂O₃-excess specimen, a second phase (yttrium aluminum perovskite: YAP) containing silicon in the grain boundary was found, (ii) For the Al₂O₃-excess specimen, both aluminum-rich particles (alumina) and a silicon-rich segregant layer were observed in the grain boundary. The volume diffusion of the oxygen tracer is little influenced by the excess composition. In contrast, the grain boundary diffusion of the oxygen tracer is suppressed in the Y₂O₃-excess specimens, compared to Al₂O₃-excess specimens. These differences are thought to result from the chemical reaction between the second phase and the intergranular liquid phase during the sintering.     

Study on ozone treatment of water-soluble polymers. I. Ozone degradation of polyethylene glycol in water

Polyethylene glycol (molecular weight 8000) was degraded by ozone in 1% aqueous solution of pH 12. Chemical oxygen demand of the solution decreased with increasing ozone consumed. Intrinsic viscosity of the solution lowered exponentially as a result of the ozonization. The number of breaks calculated from the viscosity indicated that two molecules of ozone were consumed for one cleavage of the polymer chain. The molecular weight distribution obtained by gel permeation chromatography was very broadened and molecular weight was lower as well, and the polymer chain was found to be cleaved randomly by ozone. The production of formic ester, ethylene glycol, diethylene glycol, triethylene glycol, and hydrogen peroxide was confirmed by IR, NMR, gas chromatography, and chemical analysis. These observations could be accounted for by electrophilic attack of ozone on the ether bond.     

Hydrothermal Formation of Hydroxyapatite Layers on the Surface of Type-A Zeolite

Type-A zeolite evenly covered with hydroxyapatite thin layers was prepared using hydrothermal treatment at 120°C for 8 h under autogenous pressure. The hydroxyapatite needlelike nanocrystals, 100–200 nm in diameter and 30 nm in thickness, were grown under the reaction between discharged Ca²⁺ ions from type-A zeolite and PO₄³⁻ ions in (NH₄)₃PO₄ solution. The preferential orientations of the c -axis of hydroxyapatite crystals perpendicular to a zeolite surface were observed using transmission electron microscopy. The crystal structure of type-A zeolite was not destroyed under the reaction, but the surface morphology was changed only with complete covering of scaly hydroxyapatite particles.     

Effects of free stream turbulence on a turbulent boundary layer on a flat plate with zero pressure gradient part IV: Calculation of the flow field

The effects of free stream turbulence on a turbulent boundary layer were calculated by using a k-ϵ two-equation model. The calculations were performed with respect to velocity profiles on a flat plate, wall shear stress, turbulence energy, integral length scales of turbulence, and decay of free stream turbulence, and the results were compared with the experimental results. The energy of the free stream turbulence and the dissipation values at the leading edge of the flat plate were used as the initial calculation conditions. These initial values of dissipation were determined from the integral length scales of the free stream turbulence at the leading edge. The calculated wall shear stress increased with the free stream turbulence and integral length scales of turbulence. The velocity profiles and turbulence energy agreed well with the experimental results, and the effects of free stream turbulence on the wall shear stress agreed fairly well with those observed in experiments. © 1997 Scripta Technica. Inc. Heat Trans Jpn Res. 25 (2): 65–75, 1996     

Self-assembly phenomenon of hydroxyapatite nanocrystals on chondroitin sulfate

Self-assembly phenomenon of hydroxyapatite (HAp) nanocrystals on chondroitin sulfate (ChS) templates was investigated. A HAp/ChS hybrid was synthesized through a precipitation method with a calcium hydroxide suspension and phosphoric acid solution containing the ChS. The preferential alignment of the crystallographic c-axis of the HAp crystals parallel to the long axis direction of the ChS templates was observed to occur with the chemical interactions between the HAp crystals and the functional groups of the ChS. This phenomenon was interpreted by the crystallochemical specific nucleation and growth of the HAp crystals regulated by the pre-organized functional groups of the ChS template. Practical implication may involve a biomimetic artificial bone or cartilage can be made through a precipitation method with suitable bio-organics.     

Crystal growth and structure analysis of twin-free monoclinic hydroxyapatite

Single crystals of hydroxyapatite were grown by a flux method using Ca₃(PO₄)₂ and Ca(OH)₂ under 100 MPa of Ar gas. The crystals obtained had stoichiometric composition of Ca₁₀(PO₄)₆(OH)₂ and some of them were twin-free single crystals. From X-ray diffraction analyses, the space group was confirmed to be monoclinic P2₁/b with cell parameters a=0.9419(3) nm, b=1.8848(6) nm, c=0.6884(2) nm, and =119.98(2)°. The detailed crystal structure was determined with a reliability factor R_w=0.033; the O atoms of OH were located just on the 2₁ axis while the H atoms of OH occupied the positions a little deviated from the 2₁ axis. The origin of this structure was ascribed to the formation of hydrogen bonds between the H atoms of the OH ions and the specific O atoms of the PO₄ ions.     

Toward ideal (trans)esterification by use of fluorous distannoxane catalysts

1,3-Disubstituted tetrakis(fluoroalkyl)distannoxanes, (XR(2)SnOSnR(2)Y)(2) (R = C(6)F(13)C(2)H(4) and C(4)F(9)C(2)H(4)), are highly fluorophilic and exhibit large partition coefficients in favor of fluorocarbon solvents over common organic solvents due to a double-layered structure where the stannoxane core is covered by fluoroalkyl groups. Under catalysis of these Lewis acids, fluorous technology allows novel transesterification and esterification in which a 100% yield of the desired esters is achievable with reactants in a strict 1:1 ratio. The catalysts are recovered from the fluorous phase quantitatively. More practically, the catalyst in fluorocarbon solution can be recycled for use in the next reaction repeatedly.     

Oxygen Diffusion in Single- and Poly-Crystalline Zinc Oxides

¹⁸O diffusion coefficients were measured in zinc oxide ceramics using a secondary ion mass spectrometer. The results are interpreted as indicating extrinsic behavior. The values of the lattice diffusion coefficients with higher valence dopants compared with zinc ions are greater than lower valence dopant such as lithium ions. Using the data at deeper depth, the grain boundary diffusivity of oxide ions was also evaluated. Although the lattice diffusion coefficients varied by two orders of magnitude, the products of grain boundary width and grain boundary diffusion coefficient were less sensitive to the type of dopants.     

Fluorous Surface‐Active Distannoxane Catalysts

Fluorous distannoxanes (XR^f₂SnOSnR^f₂X)₂⋅n H₂O (R_f=C₆F₁₃C₂H₄) ( 1 : X=C₈F₁₇SO₃, n=10; 4 : X=Cl, n=0) ( 1 ) catalyze the Mukaiyama aldol reaction and the allylation of aldehydes with tetraallyltin at room temperature in fluorous/organic biphasic solvent systems, in which the reactions proceed more rapidly than in a single organic or fluorous solvent. Due to the unique surface activity of 1 , the catalyst, organic substrate(s), and reagent(s) are distributed in both organic and fluorous phases to facilitate smooth reactions. Upon dilution with toluene after the reaction, the catalyst concentrates to the fluorous phase, while the organic substances migrate to the organic phase to effect facile catalyst recovery and recycling. By virtue of such a unique solvophilicity, a new version of fluorous biphase technology has been developed.