Titanate Ceramics from Wet-Chemically Prepared Powders

1994 ◽  
Vol 346 ◽  
Author(s):  
C.H. Lin ◽  
T.S. Yan
Keyword(s):  
Particle Size ◽  
Reaction Time ◽  
Raw Materials ◽  
Size Composition ◽  
Dissipation Factor ◽  
Simple Method ◽  
Chemically Reacting ◽  
Titanate Ceramics ◽  
Sintering Method ◽  
By Products

ABSTRACTA simple method of producing very fine, homogeneous BaxSr1-xTiO3 powders was developed in this study by wet-chemically reacting Ti(0H)4-xH2O, Ba(OH)2, and Sr(OH)2 as raw materials under 100°C. Relationships were obtained between particle size, composition, and reaction temperatures, reaction tunes, Sr/Ba ratios, and (Ba+Sr)/Ti ratios of the solution.Experimental results indicated that the particle size, which was around 40 nm, was both proportional to the reaction temperature as well as independant of the reaction time. In light of the varying reactivities of Ba and Sr towards Ti, reaction time was found to be a primary factor which controls the precise Ba/Sr ratio and (Ba+Sr)/Ti ratio of the titanate powder. A suitable reaction condition was observed to have prevented by-products Ba6Ti17O40 or Ba2Ti04 from being formed.The titanate powders were compressed and sintered for various temperatures. The compressibility and the sinterability of the powders were obtained. The microstrucure, dielectric constant and dissipation factor of the titanate ceramics ware observed and measured. These values sufficiently correlated with those of the titanate ceramics produced from the powders by the solid-state sintering method.

Statistical Modelling of the Particle Size Composition of an Alumina Matrix for No-Cement Self-Flowing Refractory Castables

2006 ◽  
Vol 514-516 ◽  
pp. 604-608 ◽  
Author(s):  
Abílio P. Silva ◽  
Ana M. Segadães ◽  
Tessaleno C. Devezas
Keyword(s):  
Particle Size ◽  
Water Content ◽  
Raw Materials ◽  
Size Composition ◽  
Statistical Modelling ◽  
Matrix Composition ◽  
Mechanical Resistance ◽  
Particle Size Composition ◽  
Refractory Castables ◽  
System Properties

In the processing of any particulate system (including refractory castables), the finer sized particle fraction (matrix or filler) is mostly responsible for the final system properties. Alumina fine powders were used in this work as raw materials, namely two tabular alumina fractions (–500 mesh and –230 mesh) and a commercial reactive alumina. Statistical modelling and the Response Surface Methodology (Statistica, Mixtures Designs and Triangular Surfaces module) were used to optimise the particle size composition of the three-component mixtures leading to matrix maximum flowability. The mixing methodology, aimed at minimising the water content, was kept constant. No-cement alumina castables produced with the various fine size powder mixtures, were used to prepare test-pieces. After drying and sintering, their mechanical resistance (MoR), density, porosity, water absorption, thermal shock behaviour and microstructure were evaluated. The results obtained evidenced the relevance of variables such as the water content per unit specific surface area, needed to reach the self-flow “turning point”, and validated the statistical optimisation method used. Moreover those results showed the existence of a matrix composition range, which favours the formation of a flow-bed that enables the aggregate self-flow.

Experimental Investigations on Expansion Performance of Alkali-Aggregate Reaction of Mortar

2013 ◽  
Vol 405-408 ◽  
pp. 2719-2723
Author(s):  
Feng Ouyang ◽  
Da Chen ◽  
Ying Di Liao ◽  
Chao Hua Jiang
Keyword(s):  
Particle Size ◽  
Reaction Time ◽  
Volume Expansion ◽  
Size Composition ◽  
Expansion Ratio ◽  
Experimental Investigations ◽  
Distinguishing Characteristic ◽  
Alkali Aggregate Reaction ◽  
Result Show ◽  
Function Relationship

Volume expansion is the distinguishing characteristic of concrete occurring AAR. Expansion performance of mortar with different particle size composition aggregate was tested in this paper. The result show that MR specimens with part alkali active sand and R specimens with total alkali active sand present obvious expansion. But expansion ratio of NR specimen with inactive sand remains generally stable and is only 0.02%. Ultimate expansion ratio of specimen due to AAR is not in proportion to content of alkali active aggregate. There is a possible ratio for alkali active aggregate and inactive aggregate to acquire a larger ultimate expansion account. Furthermore, expansion ratio of specimens due to AAR and reaction time present the exponential function relationship.

Design of the Particle Size Composition of an Alumina Powder Matrix for Maximum Flowability and Minimum Water Content

2006 ◽  
Vol 530-531 ◽  
pp. 425-430 ◽  
Author(s):  
Abílio P. Silva ◽  
Ana M. Segadães ◽  
Tessaleno C. Devezas
Keyword(s):  
Particle Size ◽  
Water Content ◽  
Raw Materials ◽  
Size Composition ◽  
Statistical Modelling ◽  
Linear Shrinkage ◽  
Response Surfaces ◽  
Alumina Powder ◽  
Particle Size Composition ◽  
The Matrix

In this work, commercial alumina fine powders were used as raw materials, namely two tabular alumina fractions (–500 mesh and –230 mesh) and a reactive alumina. Statistical modelling and the Response Surface Methodology (Statistica, Mixtures Designs and Triangular Surfaces module) were applied to three-component mixtures and used to calculate the various property-composition surfaces. To that aim, the various mixtures were prepared, cast, dried, fired and characterised. The particle size distribution modulus, q, was determined for all mixtures using the software LISA. The various response surfaces were then combined, so that the water content in the mixture could be minimised and the matrix flowability maximised. The properties of the resulting test-bricks (linear shrinkage, mechanical strength, apparent density and porosity) were also modelled and response surfaces were obtained. Combined results enabled the definition of an optimised particle size composition range, which guarantees the presence of a low water flow-bed that enables the aggregate self-flow.

Microstructural characterization of laser-melted/roller-quenched dicalcium silicate

1988 ◽  
Vol 46 ◽  
pp. 582-583
Author(s):  
C. J. Chan ◽  
K. R. Venkatachari ◽  
W. M. Kriven ◽  
J. F. Young
Keyword(s):  
Particle Size ◽  
Raw Materials ◽  
Shape Change ◽  
Microstructural Characterization ◽  
Particle Size Effect ◽  
Dicalcium Silicate ◽  
Laser Melting ◽  
Uniform Size ◽  
Cell Shape Change ◽  
Wide Range

Dicalcium silicate (Ca2SiO4) is a major component of Portland cement. It has also been investigated as a potential transformation toughener alternative to zirconia. It has five polymorphs: α, α'H, α'L, β and γ. Of interest is the β-to-γ transformation on cooling at about 490°C. This transformation, accompanied by a 12% volume increase and a 4.6° unit cell shape change, is analogous to the tetragonal-to-monoclinic transformation in zirconia. Due to the processing methods used, previous studies into the particle size effect were limited by a wide range of particle size distribution. In an attempt to obtain a more uniform size, a fast quench rate involving a laser-melting/roller-quenching technique was investigated.The laser-melting/roller-quenching experiment used precompacted bars of stoichiometric γ-Ca2SiO4 powder, which were synthesized from AR grade CaCO3 and SiO2xH2O. The raw materials were mixed by conventional ceramic processing techniques, and sintered at 1450°C. The dusted γ-Ca2SiO4 powder was uniaxially pressed into 0.4 cm x 0.4 cm x 4 cm bars under 34 MPa and cold isostatically pressed under 172 MPa. The γ-Ca2SiO4 bars were melted by a 10 KW-CO2 laser.

Formulation and Evaluation of Atenolol Nanocrystals Using 3(2) Full Factorial Design

2020 ◽  
Vol 10 (3) ◽  
pp. 306-315
Author(s):  
Rupa Mazumder ◽  
Swarnali Das Paul
Keyword(s):  
Particle Size ◽  
Zeta Potential ◽  
Organic Solvent ◽  
Factorial Design ◽  
Goodness Of Fit ◽  
Production Yield ◽  
Pharmacokinetic Property ◽  
Potential Yield ◽  
Simple Method ◽  
Pure Drug

Background: Atenolol is a commonly used antihypertensive drug of class III BCS category. It suffers from the problem of poor intestinal absorption or permeability thus low bioavailability. The objective of the present study was to enhance the permeability of atenolol by using a suitable technique, which is economical and devoid of using any organic solvent. Methods: The nanocrystal technology by high-pressure homogenization was chosen for this purpose, which is a less expensive and simple method. In this technique, no organic solvent was used. The study was further aimed to characterize prepared nanocrystals in the solid state by Fourier Transform Infrared Spectroscopy (FTIR), Powder X-Ray Diffraction (PXRD) patterns, particle size, zeta potential, %yield and drug permeation study through isolated goat’s intestine. An in-vivo study was carried out to determine the pharmacokinetic property in comparison to pure drug powder using rats as experimental animals. The formulation design was optimized by a 3(2) factorial design. In these designs, two factors namely surfactant amount (X1) and speed of homogenizer (X2) were evaluated on three dependent variables namely particle size (y1), zeta potential (y2) and production yield (y3). Results: PXRD study indicated the presence of high crystal content in the prepared formulation. These nanocrystal formulations were found with a narrow size range from 125 nm to 652 nm and positive zeta potential of 16-18 mV. Optimized formulations showed almost 90% production yield. Permeability study revealed 90.88% drug release for optimized formulation in comparison to the pure drug (31.22%). The FTIR study also exposed that there was no disturbance in the principal peaks of the pure drug atenolol. This confirmed the integrity of the pure drug and its compatibility with the excipients used. A significant increase in the area under the concentration-time curve Cpmax and MRT for nanocrystals was observed in comparison to the pure drug. The higher values of the determination coefficient (R2) of all three parameters indicated the goodness of fit of the 3(2) factorial model. The factorial analysis also revealed that speed of homogenizer had a bigger effect on particle size (-0.2812), zeta potential (-0.0004) and production yield (0.0192) whereas amount of surfactant had a lesser effect on production yield (-370.4401), zeta potential (-43.3651) as well as particle size (-6169.2601). Conclusion: It is concluded that the selected method of nanocrystal formation and its further optimization by factorial design was effective to increase the solubility, as well as permeability of atenolol. Further, the systematic approach of factorial design provides rational evaluation and prediction of nanocrystals formulation on the selected limited number of smart experimentation.

scholarly journals Wine By-Products as Raw Materials for the Production of Biopolymers and of Natural Reinforcing Fillers: A Critical Review

Polymers ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 381
Author(s):  
Alessandro Nanni ◽  
Mariafederica Parisi ◽  
Martino Colonna
Keyword(s):  
Critical Review ◽  
Raw Materials ◽  
Green Revolution ◽  
Building Blocks ◽  
Poly Lactic Acid ◽  
Butylene Succinate ◽  
Reinforcing Fillers ◽  
Plastic Industry ◽  
Review Reports ◽  
By Products

The plastic industry is today facing a green revolution; however, biopolymers, produced in low amounts, expensive, and food competitive do not represent an efficient solution. The use of wine waste as second-generation feedstock for the synthesis of polymer building blocks or as reinforcing fillers could represent a solution to reduce biopolymer costs and to boost the biopolymer presence in the market. The present critical review reports the state of the art of the scientific studies concerning the use of wine by-products as substrate for the synthesis of polymer building blocks and as reinforcing fillers for polymers. The review has been mainly focused on the most used bio-based and biodegradable polymers present in the market (i.e., poly(lactic acid), poly(butylene succinate), and poly(hydroxyalkanoates)). The results present in the literature have been reviewed and elaborated in order to suggest new possibilities of development based on the chemical and physical characteristics of wine by-products.

scholarly journals Leaching Behaviour of Construction and Demolition Wastes and Recycled Aggregates: Statistical Analysis Applied to the Release of Contaminants

2021 ◽  
Vol 11 (14) ◽  
pp. 6265
Author(s):  
Alessandra Diotti ◽  
Giovanni Plizzari ◽  
Sabrina Sorlini
Keyword(s):  
Particle Size ◽  
Statistical Analysis ◽  
Raw Materials ◽  
Primary Source ◽  
Recycled Aggregates ◽  
Critical Parameters ◽  
Material Particle ◽  
Analysis Methodology ◽  
Construction And Demolition Wastes ◽  
Leaching Behaviour

Construction and demolition wastes represent a primary source of new alternative materials which, if properly recovered, can be used to replace virgin raw materials partially or totally. The distrust of end-users in the use of recycled aggregates is mainly due to the environmental performance of these materials. In particular, the release of pollutants into the surrounding environment appears to be the aspect of greatest concern. This is because these materials are characterized by a strong heterogeneity which can sometimes lead to contaminant releases above the legal limits for recovery. In this context, an analysis of the leaching behaviour of both CDWs and RAs was conducted by applying a statistical analysis methodology. Subsequently, to evaluate the influence of the particle size and the volumetric reduction of the material on the release of contaminants, several experimental leaching tests were carried out according to the UNI EN 12457-2 and UNI EN 12457-4 standards. The results obtained show that chromium, mercury, and COD are the most critical parameters for both CDWs and RAs. Moreover, the material particle size generally affects the release of contaminants (i.e., finer particles showed higher releases), while the crushing process does not always involve higher releases than the sieving process.

scholarly journals Feasibility of fly ash as fluxing agent in mid- and low-grade phosphate rock carbothermal reduction and its reaction kinetics

2021 ◽  
Vol 10 (1) ◽  
pp. 157-168
Author(s):  
Biwei Luo ◽  
Pengfei Li ◽  
Yan Li ◽  
Jun Ji ◽  
Dongsheng He ◽  
...  
Keyword(s):  
Particle Size ◽  
Fly Ash ◽  
Reaction Time ◽  
Carbothermal Reduction ◽  
Industrial Waste ◽  
Phosphate Rock ◽  
Molar Ratio ◽  
Low Grade ◽  
Carbon Excess ◽  
Fluxing Agent

Abstract The feasibility of industrial waste fly ash as an alternative fluxing agent for silica in carbothermal reduction of medium-low-grade phosphate ore was studied in this paper. With a series of single-factor experiments, the reduction rate of phosphate rock under different reaction temperature, reaction time, particle size, carbon excess coefficient, and silicon–calcium molar ratio was investigated with silica and fly ash as fluxing agents. Higher reduction rates were obtained with fly ash fluxing instead of silica. The optimal conditions were derived as: reaction temperature 1,300°C, reaction time 75 min, particle size 48–75 µm, carbon excess coefficient 1.2, and silicon–calcium molar ratio 1.2. The optimized process condition was verified with other two different phosphate rocks and it was proved universally. The apparent kinetics analyses demonstrated that the activation energy of fly ash fluxing is reduced by 31.57 kJ/mol as compared with that of silica. The mechanism of better fluxing effect by fly ash may be ascribed to the fact that the products formed within fly ash increase the amount of liquid phase in the reaction system and promote reduction reaction. Preliminary feasibility about the recycling of industrial waste fly ash in thermal phosphoric acid industry was elucidated in the paper.

scholarly journals Mining Wastes of an Albite Deposit as Raw Materials for Vitrified Mullite Ceramics

Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 232
Author(s):  
Pedro J. Sánchez-Soto ◽  
Eduardo Garzón ◽  
Luis Pérez-Villarejo ◽  
George N. Angelopoulos ◽  
Dolores Eliche-Quesada
Keyword(s):  
Particle Size ◽  
Raw Materials ◽  
Phase Evolution ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Mining Wastes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Maximum Value

In this work, an examination of mining wastes of an albite deposit in south Spain was carried out using X-ray Fluorescence (XRF), X-ray diffraction (XRD), particle size analysis, thermo-dilatometry and Differential Thermal Analysis (DTA) and Thermogravimetric (TG) analysis, followed by the determination of the main ceramic properties. The albite content in two selected samples was high (65–40 wt. %), accompanied by quartz (25–40 wt. %) and other minor minerals identified by XRD, mainly kaolinite, in agreement with the high content of silica and alumina determined by XRF. The content of Na2O was in the range 5.44–3.09 wt. %, being associated with albite. The iron content was very low (<0.75 wt. %). The kaolinite content in the waste was estimated from ~8 to 32 wt. %. The particle size analysis indicated values of 11–31 wt. % of particles <63 µm. The ceramic properties of fired samples (1000–1350 °C) showed progressive shrinkage by the thermal effect, with water absorption and open porosity almost at zero at 1200–1250 °C. At 1200 °C, the bulk density reached a maximum value of 2.38 g/cm3. An abrupt change in the phase evolution by XRD was found from 1150 to 1200 °C, with the disappearance of albite by melting in accordance with the predictions of the phase diagram SiO2-Al2O3-Na2O and the system albite-quartz. These fired materials contained as main crystalline phases quartz and mullite. Quartz was present in the raw samples and mullite was formed by decomposition of kaolinite. The observation of mullite forming needle-shape crystals was revealed by Scanning Electron Microscopy (SEM). The formation of fully densified and vitrified mullite materials by firing treatments was demonstrated.

scholarly journals Effect of Sintering Temperature on Microstructure and Mechanical Properties of Hot-Pressed Fe/FeAl2O4 Composite

Crystals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 422
Author(s):  
Kuai Zhang ◽  
Yungang Li ◽  
Hongyan Yan ◽  
Chuang Wang ◽  
Hui Li ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Bending Strength ◽  
Sintering Temperature ◽  
Raw Materials ◽  
Hot Press ◽  
Microstructure And Mechanical Properties ◽  
Powder Particles ◽  
Hot Press Sintering ◽  
Sintering Method

An Fe/FeAl2O4 composite was prepared with Fe-Fe2O3-Al2O3 powder by a hot press sintering method. The mass ratio was 6:1:2, sintering pressure was 30 MPa, and holding time was 120 min. The raw materials for the powder particles were respectively 1 µm (Fe), 0.5 µm (Fe2O3), and 1 µm (Al2O3) in diameter. The effect of sintering temperature on the microstructure and mechanical properties of Fe/FeAl2O4 composite was studied. The results showed that Fe/FeAl2O4 composite was formed by in situ reaction at 1300 °C–1500 °C. With the increased sintering temperature, the microstructure and mechanical properties of the Fe/FeAl2O4 composite showed a change law that initially became better and then became worse. The best microstructure and optimal mechanical properties were obtained at 1400 °C. At this temperature, the grain size of Fe and FeAl2O4 phases in Fe/FeAl2O4 composite was uniform, the relative density was 96.7%, and the Vickers hardness and bending strength were 1.88 GPa and 280.0 MPa, respectively. The wettability between Fe and FeAl2O4 was enhanced with increased sintering temperature. And then the densification process was accelerated. Finally, the microstructure and mechanical properties of the Fe/FeAl2O4 composite were improved.

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