PL399743A1 - Method for producing porous sinters - Google Patents
Method for producing porous sintersInfo
- Publication number
- PL399743A1 PL399743A1 PL399743A PL39974312A PL399743A1 PL 399743 A1 PL399743 A1 PL 399743A1 PL 399743 A PL399743 A PL 399743A PL 39974312 A PL39974312 A PL 39974312A PL 399743 A1 PL399743 A1 PL 399743A1
- Authority
- PL
- Poland
- Prior art keywords
- hour
- temperature
- mixture
- ceramic powder
- metal
- Prior art date
Links
Abstract
Przedmiotem wynalazku jest sposób wytwarzania porowatych spieków majacych zastosowanie w chirurgii kostnej lub ukladach filtrujacych. Sposób wytwarzania porowatych spieków, polega na tym, ze proszek metalowy lub ceramiczny, lub mieszanina proszków metalowo-ceramicznych mieszany jest z krysztalami sacharozy, korzystnie cukru spozywczego o wielkosci krysztalów sacharozy 1-1,5 mm, korzystnie 1 mm w proporcji wagowej 1:1 oraz z dodatkiem 2-3 kropel alkoholu etylowego na 10 g mieszaniny, nastepnie mieszanina prasowana jest pod cisnieniem 500-700 MPa, po czym otrzymana wypraske umieszcza sie w poruszanej mieszadlem magnetycznym wodzie destylowanej o temperaturze 50-80°C, w czasie 1-2 h. Nastepnie wypraske suszy w temperaturze 60-80°C, dalej nagrzewa sie w ciagu 1 h od temperatury pokojowej do temperatury spiekania wlasciwej dla danego materialu w zakresie 1250-1300°C, przetrzymuje w tej temperaturze przez 1 h w atmosferze ochronnej, korzystnie w argonie, nastepnie spieki schladza sie w ciagu 1 h do temperatury pokojowej.The present invention relates to a method for the production of porous sinters for use in bone surgery or filtration systems. The method for producing porous sinters is that the metal or ceramic powder or metal-ceramic powder mixture is mixed with sucrose crystals, preferably food sugar with a size of 1-1.5 mm, preferably 1 mm, 1: 1 weight ratio and with the addition of 2-3 drops of ethyl alcohol per 10 g of the mixture, then the mixture is pressed under 500-700 MPa pressure, after which the obtained compact is placed in distilled water moved with a magnetic stirrer at a temperature of 50-80 ° C, during 1-2 h. The compact is then dried at 60-80 ° C, further heated within 1 hour from room temperature to the sintering temperature appropriate for the given material in the range 1250-1300 ° C, kept at this temperature for 1 hour in a protective atmosphere, preferably at argon, then the sintered is cooled to room temperature within 1 hour.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL399743A PL399743A1 (en) | 2012-07-02 | 2012-07-02 | Method for producing porous sinters |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL399743A PL399743A1 (en) | 2012-07-02 | 2012-07-02 | Method for producing porous sinters |
Publications (1)
Publication Number | Publication Date |
---|---|
PL399743A1 true PL399743A1 (en) | 2014-01-07 |
Family
ID=49877209
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL399743A PL399743A1 (en) | 2012-07-02 | 2012-07-02 | Method for producing porous sinters |
Country Status (1)
Country | Link |
---|---|
PL (1) | PL399743A1 (en) |
-
2012
- 2012-07-02 PL PL399743A patent/PL399743A1/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Li et al. | Spark plasma sintering behavior of AlON ceramics doped with different concentrations of Y2O3 | |
Bai et al. | Fabrication of highly dense Al2O3 ceramics | |
Zhou et al. | Fabrication and characterization of pure porous Ti3SiC2 with controlled porosity and pore features | |
CL2011002329A1 (en) | Method for the preparation of an instant coffee powder comprising: providing a spray-free porous powder having a particle porosity of at least 35%, an ice crystal pore volume of less than 2.5 ml / g , an ice crystal pore size of less than 3um; sintering at 0 ° C while the gas is forced through the layer; dehydrate by freezing. | |
Ahn et al. | Production of highly porous titanium (Ti) scaffolds by vacuum-assisted foaming of titanium hydride (TiH2) suspension | |
Carbajal et al. | Role of ZnO additions on the β/α phase relation in TCP based materials: Phase stability, properties, dissolution and biological response | |
Sengupta et al. | Preparation and characterization of sintered bioactive borate glass tape | |
Flauder et al. | β-TCP scaffolds with an interconnected and aligned porosity fabricated via ice-templating | |
RU2008137342A (en) | METHOD FOR PRODUCING POROUS TITANIUM NICKELIDE | |
PL399743A1 (en) | Method for producing porous sinters | |
Pan et al. | Effects of silica sol on the microstructure and mechanical properties of CaSiO3 bioceramics | |
Zhao et al. | Preparation and characterization of novel tricalcium silicate bioceramics | |
CN106007774A (en) | Preparation method of porous silicon nitride ceramic | |
Tolouei et al. | Effect of nano silica on the sinterability of hydroxyapatite dense bodies | |
张乐 et al. | Preparation and characterization of monodispersed and spherical yag powder for transparent ceramic by spray drying | |
CN104311140B (en) | A kind of silicon nitride, silicon carbide are in conjunction with the preparation method of titanium carbide foamed ceramics | |
MX2015001840A (en) | Process for producing porous metal composites with hydroxyapatite for implants and the metal-hydroxyapatite composite. | |
Döbelin et al. | Recrystallization of amorphized α-TCP | |
Lee et al. | A Study on Mechanical and Tribological Properties of Hot pressed Al2O3/ZrO2/h-BN/TiO2 Composites | |
Mangkonsu et al. | The Effect of Heating Rate and Temperature on Mechanical and Microstructure Properties of β-TCP by Microwave Sintering | |
Zhang et al. | Effects of Cr2O3 addition on mechanical and electrical properties of alumina ceramic | |
Yang et al. | Study on preparation of Y-TZP ceramic matrix for dental prosthesis. | |
LV14533A (en) | Lead-less segnetoelectric ceramic based on alkaline metal niobate and method for producing thereof | |
Lin et al. | Influence of Ca2P2O7 on Sintering Ability, Mechanical Strength and Degradability of β-Ca3 (PO4) 2 Bioceramics | |
PL421377A1 (en) | Method for producing SiAlON compounds with low thermal conductivity |