Effects of Dispersed Al2O3 Particles on Sintering of LTCC

2008 ◽  
Vol 39-40 ◽  
pp. 375-380
Author(s):  
Ralf Müller ◽  
Stefan Reinsch ◽  
Markus Eberstein ◽  
Joachim Deubener ◽  
A. Thiel ◽  
...  
Keyword(s):  
Volume Fraction ◽  
Al2o3 Particle ◽  
Model Composite ◽  
Heating Microscopy ◽  
Glass Crystal ◽  
Rate Controlled ◽  
Higher Temperature ◽  
Crystal Particle ◽  
Kinetics Of ◽  
Glass Viscosity

The sintering of Low Temperature Co-fired Ceramics prepared from alumoborosilicate glass- and Al2O3 powders of similar small particle size was studied by dilatometry, heating microscopy, microstructure analysis, glass- and effective viscosity measurements. The steric effect of Al3O3 inclusions was studied using a “non-reactive” model composite. With increasing Al3O3 volume fraction ( Φ ≤ 0.45), sintering decelerates and its final stage shifts to higher temperature. The attainable shrinkage is reduced as Al2O3 particle clusters bearing residual pores become more frequent. The kinetics of sintering could be described formally superposing the weighed contributions of differentially sized and randomly composed glass-crystal particle clusters and assuming a sintering rate controlled by the effective matrix viscosity, which increases with Φ and with progressive wetting of Al2O3 particles during densification. The “reactive” model composite shows significant dissolution of Al2O3 into the glass, which has two opposed effects on sintering: reducing Φ and increasing glass viscosity. For the present case ( Φ = 0.25), the latter effect dominates and sintering is retarded by Al2O3 dissolution. Crystallization of wollastonite starts after full densification. Dissolution of Al2O3 was found to promote the subsequent growth of anorthite.

Kinetics of carbon monoxide methanation on a Ni/SiO2 catalyst

1990 ◽  
Vol 55 (7) ◽  
pp. 1678-1685
Author(s):  
Vladimír Stuchlý ◽  
Karel Klusáček
Keyword(s):  
Carbon Monoxide ◽  
Reaction Rate ◽  
Catalyst Activity ◽  
Adsorbed Hydrogen ◽  
Reaction Products ◽  
Co Methanation ◽  
Molar Ratios ◽  
Rate Determining Step ◽  
Higher Temperature ◽  
Kinetics Of

Kinetics of CO methanation on a commercial Ni/SiO2 catalyst was evaluated at atmospheric pressure, between 528 and 550 K and for hydrogen to carbon monoxide molar ratios ranging from 3 : 1 to 200 : 1. The effect of reaction products on the reaction rate was also examined. Below 550 K, only methane was selectively formed. Above this temperature, the formation of carbon dioxide was also observed. The experimental data could be described by two modified Langmuir-Hinshelwood kinetic models, based on hydrogenation of surface CO by molecularly or by dissociatively adsorbed hydrogen in the rate-determining step. Water reversibly lowered catalyst activity and its effect was more pronounced at higher temperature.

scholarly journals Continuous Cooling Transformation Behaviour and Bainite Transformation Kinetics of 23CrNi3Mo Carburised Steel

Metals ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 48
Author(s):  
Wenjun Song ◽  
Min Lei ◽  
Mingpan Wan ◽  
Chaowen Huang
Keyword(s):  
Phase Transformation ◽  
Volume Fraction ◽  
Austenite Formation ◽  
Steel Matrix ◽  
Transformation Kinetics ◽  
Bainite Transformation ◽  
Continuous Cooling ◽  
The Matrix ◽  
Dimensional Growth ◽  
Kinetics Of

In this study, the phase transformation behaviour of the carburised layer and the matrix of 23CrNi3Mo steel was comparatively investigated by constructing continuous cooling transformation (CCT) diagram, determining the volume fraction of retained austenite (RA) and plotting dilatometric curves. The results indicated that Austenite formation start temperature (Ac1) and Austenite formation finish temperature (Ac3) of the carburised layer decreased compared to the matrix, and the critical cooling rate (0.05 °C/s) of martensite transformation is significantly lower than that (0.8 °C/s) of the matrix. The main products of phase transformation in both the carburised layer and the matrix were martensite and bainite microstructures. Moreover, an increase in carbon content resulted in the formation of lamellar martensite in the carburised layer, whereas the martensite in the matrix was still lath. Furthermore, the volume fraction of RA in the carburised layer was higher than that in the matrix. Moreover, the bainite transformation kinetics of the 23CrNi3Mo steel matrix during the continuous cooling process indicated that the mian mechanism of bainite transformation of the 23CrNi3Mo steel matrix is two-dimensional growth and one-dimensional growth.

scholarly journals Pyrolysis and Oxidation of PAN in Dry Air. Thermoanalytical Methods

1970 ◽  
Vol 17 (1) ◽  
pp. 38-42
Author(s):  
Anna BIEDUNKIEWICZ ◽  
Pawel FIGIEL ◽  
Marta SABARA
Keyword(s):  
Temperature Increase ◽  
Heating Rates ◽  
Linear Change ◽  
Dry Air ◽  
Isothermal Conditions ◽  
Gaseous Products ◽  
Heterogeneous Processes ◽  
Temperature Ranges ◽  
Higher Temperature ◽  
Kinetics Of

The results of investigations on pyrolysis and oxidation of pure polyacrylonitrile (PAN) and its mixture with N,N-dimethylformamide (DMF) under non-isothermal conditions at linear change of samples temperature in time are presented. In each case process proceeded in different way. During pyrolysis of pure PAN the material containing mainly the product after PAN cyclization was obtained, while pyrolysis of PAN+DMF mixture gave the product after cyclization and stabilization. Under conditions of measurements, in both temperature ranges, series of gaseous products were formed.For the PAN-DMF system measurements at different samples heating rates were performed. The obtained results were in accordance with the kinetics of heterogeneous processes theory. The process rates in stages increased along with the temperature increase, and TG, DTG and HF function curves were shifted into higher temperature range. This means that the process of pyrolysis and oxidation of PAN in dry air can be carried out in a controlled way.http://dx.doi.org/10.5755/j01.ms.17.1.246

Diffusion Enhancement in Glassy Metals Under Non-Equilibrium Conditions

1995 ◽  
Vol 400 ◽  
Author(s):  
S. Bellini ◽  
G. Mazzone ◽  
A. Montone ◽  
M. Vittori-antisari Enea ◽  
C.R. Casaccia
Keyword(s):  
Free Volume ◽  
Growth Kinetics ◽  
Bulk Diffusion ◽  
High Energy ◽  
First Case ◽  
Diffusion Enhancement ◽  
Glass Crystal ◽  
Kinetics Of ◽  
Crystal Interface ◽  
Diffusion Properties

AbstractThe diffusion properties of a Ni-Zr metallic glass formed at the interface of a bulk diffusion couple have been studied in conditions far from a fully relaxed state. The growth kinetics of the interface film have been enhanced by both plastic deformation and high energy electron irradiation. Different results have been obtained in the two cases, since in the first case the film grows exponentially with time, while in the second case the usual square root dependence on time is observed. This behaviour has been interpreted as a consequence of the annihilation kinetics of the excess free volume introduced in the glass by the above methods. Two different mechanisms of free volume annihilation , namely exchange with a crystal vacancy at the glass-crystal interface and structural relaxation in the bulk glassy phase have been considered to be operative so that the nature of the growth kinetics has been found to depend on the mechanism predominant in each experimental condition.

Joining of Ti3SiC2 with Ti–6Al–4V Alloy

2002 ◽  
Vol 17 (1) ◽  
pp. 52-59 ◽  
Author(s):  
N.F. Gao ◽  
Y. Miyamoto
Keyword(s):  
Solid State ◽  
Rate Constant ◽  
Liquid State ◽  
Parabolic Rate Constant ◽  
Diffusion Path ◽  
Solid State Diffusion ◽  
Diffusion Controlled ◽  
State Diffusion ◽  
Rate Controlled ◽  
Higher Temperature

The joining of a Ti3SiC2 ceramic with a Ti–6Al–4V alloy was carried out at the temperature range of 1200–1400 °C for 15 min to 4 h in a vacuum. The total diffusion path of joining was determined to be Ti3SiC2/Ti5Si3Cx/Ti5Si3Cx + TiCx/TiCx/Ti. The reaction was rate controlled by the solid-state diffusion below 1350 °C and turned to the liquid-state diffusion controlled with a dramatic increase of parabolic rate constant Kp when the temperature exceeded 1350 °C. The TiCx tended to grow at the boundarywith the Ti–6Al–4V alloy at a higher temperature and longer holding time. TheTi3SiC2/Ti–6Al–4V joint is expected to be applied to implant materials.

scholarly journals Chicken Intestinal Alkaline Phosphatase

1960 ◽  
Vol 43 (6) ◽  
pp. 1149-1169 ◽  
Author(s):  
M. Kunitz
Keyword(s):  
Alkaline Phosphatase ◽  
Zinc Ions ◽  
Magnesium Ions ◽  
Intestinal Alkaline Phosphatase ◽  
Reversible Inactivation ◽  
Higher Temperature ◽  
Kinetics Of ◽  
Hydrolysis Of ◽  
Zn Ions ◽  
Denaturation Of Proteins

Purified chicken intestinal alkaline phosphatase is active at pH 8 to 9, but becomes rapidly inactivated with change of pH to 6 or less. Also, a solution of the inactivated enzyme at pH 4.5 rapidly regains its activity at pH 8. In the range of pH 6 to 8 a solution of purified alkaline phosphatase consists of a mixture of active and inactive enzyme in equilibrium with each other. The rate of inactivation at lower pH and of reactivation at higher pH increases with increase in temperature. Also, the activity at equilibrium in the range of pH 6 to 8 increases with temperature so that a solution equilibrated at higher temperature loses part of its activity on cooling, and vice versa, a rise in temperature shifts the equilibrium toward higher activity. The kinetics of inactivation of the enzyme at lower pH and the reactivation at higher pH is that of a unimolecular reaction. The thermodynamic values for the heat and entropy of the reversible inactivation and reactivation of the enzyme are considerably lower than those observed for the reversible denaturation of proteins. The inactivated enzyme at pH 4 to 6 is rapidly reactivated on addition of Zn ions even at pH 4 to 6. However, zinc ions are unable to replace magnesium ions as cocatalysts for the enzymatic hydrolysis of organic phosphates by alkaline phosphatase.

The Self-Decay Characteristics of Chlorine Dioxide in Water

2012 ◽  
Vol 610-613 ◽  
pp. 296-299
Author(s):  
Xin Jie Li ◽  
Dan Nan Jiang ◽  
Yue Jun Zhang
Keyword(s):  
Rate Constants ◽  
Tap Water ◽  
Pure Water ◽  
Decay Behaviour ◽  
Increase With Increase ◽  
Higher Temperature ◽  
Effects Of Temperature ◽  
Lower Temperature ◽  
Kinetics Of ◽  
Temperature Water

In order to learn the ClO2 decay behaviour in tap water, the kinetics of ClO2 decay in pure water was studied. Under the conditions of tap water treatment and keeping away from light, the effects of temperature and pH on ClO2 degradation were investigated. The results show that the ClO2 decay reaction in pure water is the first-order with respect to ClO2, the decay rate constants increase with increase in temperature or pH. At pH=6.87, the rate constants are 0.012h-1(15°C), 0.017h-1(25°C), 0.023h-1(35°C), and 0.029h-1(45°C), respectively. At 25°C, the rate constants are 0.0083h-1(pH=4.5), 0.0111h-1(pH=5.5), 0.0143h-1(pH=6.5), 0.0222h-1(pH=7.5), and 0.0351h-1(pH=8.5), respectively. The experimental data prove that ClO2 is more stable in acidic or lower temperature water than in neutral, alkalescent, or higher temperature water.

scholarly journals On the Stability of 3C-SiC Single Crystals at High Temperatures

2012 ◽  
Vol 717-720 ◽  
pp. 493-496
Author(s):  
Deborah Dompoint ◽  
Irina G. Galben-Sandulache ◽  
Alexandre Boulle ◽  
Didier Chaussende ◽  
Dominique Eyidi ◽  
...  
Keyword(s):  
Single Crystals ◽  
Volume Fraction ◽  
Diffuse Intensity ◽  
X Ray ◽  
Partial Dislocations ◽  
X Ray Scattering ◽  
Transmission Electron ◽  
The Stability ◽  
Kinetics Of ◽  
Evolution With Time

The 3C-6H polytypic transition in 3C-SiC single crystals is studied by means of diffuse X-ray scattering (DXS) coupled with transmission electron microscopy (TEM). TEM reveals that the partially transformed SiC crystals contain regions of significantly transformed SiC (characterized by a high density of stacking faults) co-existing with regions of pure 3C-SiC. The simulation of the diffuse intensity allows to determine both the volume fraction of transformed material and the transformation level within these regions. It is further shown that the evolution with time and temperature of the transition implies the multiplication and glide of partial dislocations, the kinetics of which are quantified by means of DXS.

scholarly journals Kinetics of polymer looping with macromolecular crowding: effects of volume fraction and crowder size

Soft Matter ◽  
2015 ◽  
Vol 11 (3) ◽  
pp. 472-488 ◽  
Author(s):  
Jaeoh Shin ◽  
Andrey G. Cherstvy ◽  
Ralf Metzler
Keyword(s):  
Volume Fraction ◽  
Macromolecular Crowding ◽  
Crowding Effects ◽  
Kinetics Of

Depending on the size of crowding molecules and their volume fraction the looping rates of polymers are facilitated or impeded.

scholarly journals Static Recrystallization Microstructure Evolution in a Cold-Deformed Ni-Based Superalloy during Electropulsing Treatment

Crystals ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 884
Author(s):  
Hongbin Zhang ◽  
Chengcai Zhang ◽  
Baokun Han ◽  
Kuidong Gao ◽  
Ruirui Fang ◽  
...  
Keyword(s):  
Grain Size ◽  
Thermal Effect ◽  
Static Recrystallization ◽  
Volume Fraction ◽  
Heating Effect ◽  
Wind Force ◽  
Average Grain Size ◽  
Higher Temperature ◽  
Electropulsing Treatment ◽  
Electron Wind

The influence of electropulsing treatment (EPT) parameters on the static recrystallization (SRX) microstructure in a cold-deformed Ni-based superalloy was investigated. During EPT, both the volume fraction of SRX grains and the average grain size increased with the increasing EPT temperature, which was attributed to the thermal effect and athermal effect induced by EPT. The mobility of SRX grain boundaries was promoted at the higher temperature due to the thermal effect, while the nucleation rate would be increased by EPT through decreasing the thermodynamic barrier. The formation of parallel dislocations caused by electron wind force could also play an indirect role in promoting SRX process. Moreover, the volume fraction of SRX grains increased significantly with the extension of EPT time at 700 °C, while the EPT time had a trivial effect on the average grain size. In addition, the sufficient deformation was essential to the occurrence of SRX behavior during EPT, and the localized Joule heating effect could promote the SRX behavior in the samples with the larger strains. Besides that, the influence of twining and carbides on the SRX behaviors was also investigated.

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