Fading of azo reactive dyes by perspiration and light

The fastness of azo reactive dyes on cellulose in a combined perspiration and light test was investigated, and compared with the results obtained in a conventional light fastness test. Whereas reactive dyes containing an H-or K-acid azo chromophore performed better in the conventional light fastness test, reactive dyes of the J-or γ-acid type exhibited a higher fastness in the combined test. The results suggest that testing under combined perspiration and light conditions involves a photoreduction mechanism, but a photo-oxidation mechanism operates when dyed fabrics fade under light only.     

Sintering and Mechanical Properties of Yttria-Doped Tetragonal ZrO2 Polycrystal/Mullite Composites

Yttria-doped tetragonal ZrO₂ polycrystal (Y-TZP)lmullite composites were sintered at 1450° to 1500°C in air to disperse rodlike mullite grains at the grain boundary of Y-TZP and the mechanical and thermal properties were investigated. The aspect ratios of mullite grain were >2. High fracture strength of 1000 MPa and fracture toughness of 12 MPa·m^1/2 were obtained by dispersing <20 vol% of mullite into Y-TZP. The thermal expansion coefficient of Y-TZP/mullite composites decreased with increasing mullite content. The thermal shock resistance of Y-TZP was greatly improved by dispersion of rodlike mullite grains.     

Design, synthesis, and biological evaluation of aminoboronic acids as growth-factor receptor inhibitors of EGFR and VEGFR-1 tyrosine kinases

A series of aminoboronic acids was synthesized based on the structure of lavendustin pharmacophore 1. Their inhibitory activities against the epidermal growth-factor receptor (EGFR) and vascular endothelial growth-factor receptor-1 (VEGFR-1, Flt-1) protein tyrosine kinases, and various protein kinases, PKA, PKC, PTK, and eEF2K were evaluated. Selective inhibition activities were observed in a series of aminoboronic acids. 4-Methoxy-3-((2- methoxyphenylamino)methyl)phenylboronic acid 10 inhibited EGFR tyrosine kinase, whereas 4-(2,5-dihydroxybenzylamino)phenylboronic acid 12 inhibited Flt-1 protein kinase, although lavendustin pharmacophore 1 inhibited both EGFR and Flt-1 kinases at a compound concentration of 1.0 microg mL(-1). The selective inhibition of EGFR by 10 is considered to be due to the substitution of the dihydroxy groups on the benzyl moiety for a boronic acid group at the para position, whereas the selective inhibition of Flt-1 by 12 is due to the substitution of the carboxyl group on the aniline moiety in the lavendustin pharmacophore 1 for a boronic acid group.     

Performance of ZrC-Coated Particle Fuel in Irradiation and Postirradiation Heating Tests

The ZrC-coated UO₂ particle is a promising fuel for high-temperature gas-cooled reactors. Particle fuels with multiple layers of pyrolytic carbon and ZrC have been irratiation-tested to a maximum fast-neutron fluence exceeding 2 × 10²⁵/m² ( E < 29 fJ). In-reactor fission-gas release measured at a burnup of 1.5 at.% was minimal. The failure fraction by postirradiation examination was null for all samples. The ZrC-coated particles at 4 at.% burnup were postirradiation heated to 2400°C/min without failure until after 6000 s at the maximum temperature. It was found that the ZrC layer could sustain a large strain at such high temperatures. The behavior is in strong contrast with that of SiC of standard Triso coating, which is brittle to very high temperatures.     

Gas chromatographic separation of cholesteryl esters of fatty acids of different degrees of unsaturation

Cholesteryl esters prepared from the fatty acid methyl esters of linseed oil, pig liver lipids, and Japanese anchovy oil have been separated on the basis of their chain lengths and number of double bonds by gas lipid chromatography on a cyanosiloxane SILAR 10C column. The equivalent chain lengths of cholesteryl esters having acyl groups with 14–22 carbons and 0–6 double bonds are presented. A significant influence of the column temperature on the equivalent chain lengths of the polyenoic fatty acid cholesteryl esters has been found. Separation of the cholestanyl and epicholestanyl esters of linseed oil fatty acids, respectively, under the same conditions is also described.     

Enzymatic Production of Fatty Acid Methyl Esters by Hydrolysis of Acid Oil Followed by Esterification

Acid oil, a by-product of vegetable oil refining, was enzymatically converted to fatty acid methyl esters (FAME). Acid oil contained free fatty acids (FFA), acylglycerols, and lipophilic compounds. First, acylglycerols (11 wt%) were hydrolyzed at 30 °C by 20 units Candida rugosa lipase/g-mixture with 40 wt% water. The resulting oil layer containing 92 wt% FFA was used for the next reaction, methyl esterification of FFA to FAME by immobilized Candida antarctica lipase. A mixture of 66 wt% oil layer and 34 wt% methanol (5 mol for FFA) were shaken at 30 °C with 1.0 wt% lipase. The degree of esterification reached 96% after 24 h. The resulting reaction mixture was then dehydrated and subjected to the second esterification that was conducted with 2.2 wt% methanol (5 mol for residual FFA) and 1.0 wt% immobilized lipase. The degree of esterification of residual FFA reached 44%. The degree increased successfully to 72% (total degree of esterification 99%) by conducting the reaction in the presence of 10 wt% glycerol, because water in the oil layer was attracted to the glycerol layer. Over 98% of total esterification was maintained, even though the first and the second esterification reactions were repeated every 24 h for 40 days. The enzymatic process comprising hydrolysis and methyl esterification produced an oil containing 91 wt% FAME, 1 wt% FFA, 1 wt% acylglycerols, and 7 wt% lipophilic compounds.     

Relaxation spectrometry of polyethylene in urea-polyethylene complex by BL n.m.r. and e.s.r. measurements

The molecular motions of polyethylene in urea-polyethylene complexes have been studied by e.s.r. and BL n.m.r. The e.s.r. spectra of alkyl free radicals located along the polymer chains were recorded and the temperature dependences of hyperfine splitting widths due to the β-protons (ΔH_β1, ΔH_β2) and linewidths were estimated. A decrease in (ΔH_β1 ? ΔH_β2) and narrowing (which appears over a wide temperature region) was found. The motional narrowing of line widths in the _BL n.m.r. spectra were also found. Correlation times for the molecular motion of polyethylene molecules were calculated from this magnetic resonance data, taking into account the distribution of relaxation times according to Miyake's equation. It was concluded that the molecular motions studied by e.s.r. and n.m.r. were the same. Relaxation time spectra indicated higher activation energies (10 kcal) than those calculated for a system with a single correlation time.     

Oxidation of HIPed TiC Ceramics in Dry O2, Wet O2, and H2O Atmospheres

Isothermal oxidation of dense TiC ceramics, fabricated by hot-isostatic pressing at 1630°C and 195 MPa, was performed in Ar/O₂ (dry oxidation), Ar/O₂/H₂O (wet oxidation), and Ar/H₂O (H₂O oxidation) at 900°–1200°C. The weight change measurements of the TiC specimen showed that the dry, wet, and H₂O oxidation at 850°–1000°C is represented by a one-dimensional parabolic rate equation, while the oxidation in the three atmospheres at 1100° and 1200°C proceeds linearly. Cross-sectional observation showed that the dry oxidation produces a lamellar TiO₂ scale consisting of many thin layers, about 5 μm thick, containing many pores and large cracks, while H₂O-containing oxidation decreases pores in number and diminishes cracks in scales. Gas evolution of CO₂ and H₂ with weight change measurement was simultaneously followed by heating the TiC to 1400°C in the three atmospheres. Cracking in the TiO₂ scale accompanied CO₂ evolution, and the H₂O-containing oxidation produced a small amount of H₂. A piece of single crystal TiC was oxidized in ¹⁶O₂/H₂¹⁸O to reveal the contribution of O from H₂O to the oxidation of TiC by secondary ion mass spectrometry.