Electrical properties of silica-alumina ceramics in nitrogen atmosphere

1993 ◽  
Vol 8 (5) ◽  
pp. 1116-1121 ◽  
Author(s):  
Yoshihiro Hirata ◽  
Mitsunori Kawabata ◽  
Yoshimi Ishihara

The SiO2–Al2O3 powders with compositions of 46.5 to 76.6 wt. % Al2O3, synthesized by the hydrolysis of metal alkoxides, were sintered at 1700 °C for 3 h in a reduced pressure of 40 Pa. After sintering, the samples were annealed at 1300 °C for 10 h in air. The densities of sintered samples were higher than 97.0% T.D. The electrical conductivities of the SiO2–Al2O3 ceramics in N2 atmosphere (>99.99%) were measured in the temperature range of 500° to 800 °C by using ac bridge circuit at 120 Hz to 1 MHz and dc circuit at 1 V. The electrical conductivities at 800 °C were 3.4 × 10−7 to 4.3 × 10−6 S cm−1, and decreased with increasing Al2O3 content. The SiO2–Al2O3 ceramics were mixed conductors of oxygen ions and electrons in nitrogen atmosphere. The activation energies of ionic and electronic conductivities were 102 to 143 kJ/mole and 102 to 123 kJ/mole, respectively.

2017 ◽  
Vol 6 (4) ◽  
pp. 96 ◽  
Author(s):  
Hidetaka Noritomi ◽  
Jumpei Nishigami ◽  
Nobuyuki Endo ◽  
Satoru Kato ◽  
Katsumi Uchiyama

We have found that the organic solvent-resistance of Alpha-chymotrypsin (Alpha-CT) is enhanced by adsorbing Alpha-CT onto bamboo charcoal powder (BCP), which is obtained by pyrolyzing bamboo waste under nitrogen atmosphere, and is markedly dependent on the thermodynamic water activity (aw) in organic solvents. When BCP-adsorbed Alpha-CT was immersed in acetonitrile at an appropriate water activity, it effectively enhanced the transesterification of N-acetyl-L-tyrosine ethyl ester (N-Ac-Tyr-OEt) with n-butanol (BuOH) to produce N-acetyl-L-tyrosine butyl ester (N-Ac-Tyr-OBu), compared to the hydrolysis of N-Ac-Tyr-OEt with water to give N-acetyl-L-tyrosine (N-Ac-Tyr-OH). When the water activity was 0.28, the initial rate of transesterification catalyzed by BCP-adsorbed Alpha-CT was about sixty times greater than that catalyzed by free Alpha-CT. Regarding the reaction selectivity which is defined as a ratio of the initial rate of transesterification to that of hydrolysis, BCP-adsorbed α-CT was much superior to free Alpha-CT. The catalytic activity of BCP-adsorbed Alpha-CT was markedly dependent on the reaction temperature. Furthermore, concerning the thermal stability at 50 oC, the half-life of BCP-adsorbed Alpha-CT exhibited 3.8-fold, compared to that of free Alpha-CT.


1981 ◽  
Vol 67 (4) ◽  
pp. 325-332 ◽  
Author(s):  
Stanislav Pavel ◽  
Frits A. J. Muskiet ◽  
Alena Budešínská ◽  
Jirí Duchon

A qualitative gas chromatographic analysis of trimethylsilylated ethyl acetate extracts of melanotic urine revealed 5 indolic compounds, which have been identified as substituted 5,6-dihydroxyindoles. Ethyl acetate extracts of melanotic urines at pH 2.0 contained isomeric 5-hydroxy-6-methoxy and 6-hydroxy-5-methoxy-indolyl-2-carboxylic acids which were not separable under the conditions used. A careful hydrolysis of melanotic urine with a Helix pomatia preparation followed by extraction at pH 6.5 in a nitrogen atmosphere released 3 additional indolic compounds from their conjugated form. Using gas chromatographic-mass spectrometric analysis they were identified as 5-hydroxy-6-methoxy, 6-hydroxy-5-methoxyindole and 5,6-dihydroxyindole.


ChemInform ◽  
1987 ◽  
Vol 18 (24) ◽  
Author(s):  
S.-I. HIRANO ◽  
T. HAYASHI ◽  
T. KAGEYAMA

1970 ◽  
Vol 32 (3) ◽  
pp. 470-476 ◽  
Author(s):  
Hiroyoshi Murayama ◽  
Koichi Kobayashi ◽  
Masumi Koishi ◽  
Kenjiro Meguro

1995 ◽  
Vol 398 ◽  
Author(s):  
C. Barrera-Solano ◽  
M. PiÑero ◽  
C. Jiménez-Solís ◽  
L. Gago-Duport

ABSTRACTYSZ samples containing 5 and 10 mol% of Y203 were prepared by controlled hydrolysis of metal alkoxides. The dried powders were calcined at 800°C and then they were uniaxially pressed and sintered at different temperatures and next heated at 1400°C (∼ 5 MPa) or annealed at 1600°C for 24 h. The quantitative analysis of the experimental X-ray diffraction (XRD) spectra was performed by Whole Pattern Fitting (WPF). A Pseudo-Voigt (Thompson-Cox-Hastings) was used as shape profile function. The respective phase fractions (wt %) were fitted for both solid state solutions using the scale factor. The heat treatment induced changes are discussed.


2019 ◽  
Vol 45 (5) ◽  
pp. 5179-5188 ◽  
Author(s):  
J. Feltrin ◽  
A. De Noni ◽  
D. Hotza ◽  
J.R. Frade

1988 ◽  
Vol 23 (2) ◽  
pp. 395-399 ◽  
Author(s):  
M. I. Yanovskaya ◽  
E. P. Turevskaya ◽  
A. P. Leonov ◽  
S. A. Ivanov ◽  
N. V. Kolganova ◽  
...  

2020 ◽  
Vol 5 (2) ◽  
pp. 161-163
Author(s):  
Narayan G. Bhat ◽  
Maria Villarreal

1-Trimethyl-1-germylalkynes were synthesized by deprotonation of terminal alkynes with n-butyl lithium at low temperature followed by treatment with trimethylgermyl chloride under nitrogen atmosphere. The reagent system Cp2ZrCl2/2EtMgBr converts 1-trimethylgermyl-1-alkynes into α- trimethylgermylzirconacyclopentenes at -78 ºC for 1 h followed by stirring at room temperature overnight. These novel intermediates are hydrolyzed at 0 ºC for an hour to provide the corresponding (Z)-1-trimethylgermyl-1-alkenes in good yields (74-85%) and in high stereochemical purities (> 98%) as evidenced by 13C spectral data.


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