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Polycrystalline Dental
Ceramics
By
Mohamed Mahmoud Abdul-Monem
Dental Biomaterials Department
Faculty of Dentistry
Alexandria University
Egypt
What are polycrystalline cermaics?
• Solid-sintered, monophase ceramics are materials
that are formed by directly sintering crystals
together without any intervening matrix to from
a dense, air-free, glass-free, polycrystalline
structure.
• There are several different processing techniques
that allow the fabrication of either solid-sintered
aluminous-oxide or zirconia-oxide frameworks.
Aluminous oxide
• The first fully dense polycrystalline material
for dental applications was Procera® AllCeram
alumina (Nobel Biocare) with a strength of
approximately 600 MPa.
• The alumina powder is pressed and milled on
a die and sintered at about 1600°C, leading to
a dense coping but with approximately 20%
shrinkage
• Alumina core ceramic is indicated for anterior
and posterior crowns.
• Alumina cannot be acid etched to produce
micromechanical retention silica-coated
alumina particles thus sandblasting the
surface with is required to ensure sufficient
resin bonding.
Zirconia
• Zirconia has unique physical characteristics
that make it twice as strong and tough as
alumina-based ceramics.
• Zirconia occurs as a natural mineral called
baddeleyite. This mineral contains 80–90%
zirconium oxide. The major impurities are
usually TiO2, SiO2 and Fe2O3.
• This oxide exists in three different crystal structures:
monoclinic at room temperature, tetragonal at
~1200°C and cubic at 2370°C.
• Zirconium oxide is transformed from one crystalline
state to another during firing.
• At the firing temperature, zirconia is tetragonal and at
room temperature, it is monoclinic, with a unit cell of
monoclinic occupying about 4.4% more volume than
when tetragonal.
Zirconia phase transformation
• ZrO2 adopts a monoclinic crystal structure at room
temperature and transitions to tetragonal and cubic at
higher temperatures.
• The volume expansion caused by the cubic to tetragonal
to monoclinic transformation induces large stresses, and
these stresses cause ZrO2 to crack upon cooling from high
temperatures.
• When the zirconia is blended with some other oxides, the
tetragonal and/or cubic phases are stabilized.
• Effective stabilizers include magnesium oxide (MgO),
yttrium oxide (Y2O3, yttria), calcium oxide (CaO), and
cerium(III) oxide (Ce2O3).
• Zirconia is often more useful in its phase 'stabilized' state. Upon
heating, zirconia undergoes disruptive phase changes.
• By adding small percentages of yttria, these phase changes are
eliminated, and the resulting material has superior thermal,
mechanical, and electrical properties.
• In some cases, the tetragonal phase can be metastable. If sufficient
quantities of the metastable tetragonal phase is present, then an
applied stress, magnified by the stress concentration at a crack tip, can
cause the tetragonal phase to convert to monoclinic, with the
associated volume expansion.
• This phase transformation can then put the crack into compression,
retarding its growth, and enhancing the fracture toughness. This
mechanism is known as transformation toughening, and significantly
extends the reliability and lifetime of products made with stabilized
zirconia.
Zirconia transformation toughening
• Zirconia may be in the form of blocks that are
milled to create the frameworks (CAD/CAM).
• Mostly, they are fabricated from a porous block,
milled oversized by about 25%, and sintered to
full density in a 4 - 6 hours cycle.
• Alternatively, fully dense blocks are milled.
However, this approach requires approximately 2
hours of milling time per unit whereas milling of
the porous block necessitates only 30 to 45
minutes for a three-unit bridge.
Properties of zirconia
• Low thermal conductivity (20% that of alumina)
• Chemically inert ant corrosion resistant
• Flexural strength 900 Mpa
• Fracture toughness 8-10 MPa · m1/2
• High fracture resistance
• Wear of opposing dentition(Monolithic Zirconia)
• Difficulty in adjusting occlusion
Fracture toughness of zirconia
• Fracture toughness of zirconia tends to
increase with increasing grain size (0.9µm-1.4
µm).
• There is a decrease in strength caused by very
large grain size(1.8 µm) caused by premature
phase transformation leading to microcracking
Hydrothermal degradation of zirconia
• Hydrothermal degradation of zirconia occurs
between 200-400 ˚C .
• Longer exposure times at oral temperature
may also degrade zirconia leading to increased
surface roughness,fragmanted grains and
microcracks .
Zirconia toughened alumina ZTA
• 70-90% alumina
• 10-20% zironia
• Toughened by a stress-induced transformation
mechanism of zirconia leading to compressive
stresses within alumina.
• The strength of alumina is doubled and
toughness is increase 2-4 times .
Methods of strengthening Dental
ceramics
Strengthening
Methods
Strengthening brittle
materials
Introduction of
residual
compressive
stresses
Ion strenghtening
Thermal
compatibility
Interruption of
crack propagation
Incorporation of
crystalline phase
Heat treatment
ceramming
Methods of
designing to
Minimize tensile
stress through
design
Avoid stress raisers
1.Strengthening of brittle materials
a.Introduction of residual compressive stresses
Ion strengthening
• Replacing smaller ions
by relatively larger ones
• As a result crack growth
from surface flaws is
more difficult
Thermal compatibilty
• In PFM ,metals and
porcelain are designed
with a slight mismatch
in COTE (metal slightly
higher)
• Metal contracts more
on cooling
• This leaves porcelain in
residual compression
1.Strengthening of brittle materials
b.Interruption of crack propagation
Incorporation of crystalline
phase
• Tough crystaline material
as alumina or leucite is
added to galss in a
particulate form,the glass
is toughened and
strengthened (Dispersion
tougheneing)
Heat treatment ceramming
• A glass cerammic material
is fabricated in vitreous or
noncrystalline state and
then converted to a
crystalline state by heat
treatment to induce
partial devitrifaction
• Crystalline
particles,needles or plates
formed during ceramming
serve to interrupt cracks
2.Design of dental restorations to :
a.Minimize tensile stress
• In case of PFM ,metal
copings act as the
foundation.
• The strong yet more
ductile metal prevents
the interior of porcelain
portion of the crown from
being subjected to tensile
stresses.
b.Avoid stress raisers
• Sharp line angles in
preparation should be
removed.
• Sharp line angles in
coping surface should be
avoided
• Sudden changes in
porcelain thickness
should be avoided.
Thank you

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polycrystalline dental ceramics

  • 1. Polycrystalline Dental Ceramics By Mohamed Mahmoud Abdul-Monem Dental Biomaterials Department Faculty of Dentistry Alexandria University Egypt
  • 2. What are polycrystalline cermaics? • Solid-sintered, monophase ceramics are materials that are formed by directly sintering crystals together without any intervening matrix to from a dense, air-free, glass-free, polycrystalline structure. • There are several different processing techniques that allow the fabrication of either solid-sintered aluminous-oxide or zirconia-oxide frameworks.
  • 3. Aluminous oxide • The first fully dense polycrystalline material for dental applications was Procera® AllCeram alumina (Nobel Biocare) with a strength of approximately 600 MPa. • The alumina powder is pressed and milled on a die and sintered at about 1600°C, leading to a dense coping but with approximately 20% shrinkage
  • 4. • Alumina core ceramic is indicated for anterior and posterior crowns. • Alumina cannot be acid etched to produce micromechanical retention silica-coated alumina particles thus sandblasting the surface with is required to ensure sufficient resin bonding.
  • 5.
  • 6. Zirconia • Zirconia has unique physical characteristics that make it twice as strong and tough as alumina-based ceramics. • Zirconia occurs as a natural mineral called baddeleyite. This mineral contains 80–90% zirconium oxide. The major impurities are usually TiO2, SiO2 and Fe2O3.
  • 7. • This oxide exists in three different crystal structures: monoclinic at room temperature, tetragonal at ~1200°C and cubic at 2370°C. • Zirconium oxide is transformed from one crystalline state to another during firing. • At the firing temperature, zirconia is tetragonal and at room temperature, it is monoclinic, with a unit cell of monoclinic occupying about 4.4% more volume than when tetragonal.
  • 9. • ZrO2 adopts a monoclinic crystal structure at room temperature and transitions to tetragonal and cubic at higher temperatures. • The volume expansion caused by the cubic to tetragonal to monoclinic transformation induces large stresses, and these stresses cause ZrO2 to crack upon cooling from high temperatures. • When the zirconia is blended with some other oxides, the tetragonal and/or cubic phases are stabilized. • Effective stabilizers include magnesium oxide (MgO), yttrium oxide (Y2O3, yttria), calcium oxide (CaO), and cerium(III) oxide (Ce2O3).
  • 10. • Zirconia is often more useful in its phase 'stabilized' state. Upon heating, zirconia undergoes disruptive phase changes. • By adding small percentages of yttria, these phase changes are eliminated, and the resulting material has superior thermal, mechanical, and electrical properties. • In some cases, the tetragonal phase can be metastable. If sufficient quantities of the metastable tetragonal phase is present, then an applied stress, magnified by the stress concentration at a crack tip, can cause the tetragonal phase to convert to monoclinic, with the associated volume expansion. • This phase transformation can then put the crack into compression, retarding its growth, and enhancing the fracture toughness. This mechanism is known as transformation toughening, and significantly extends the reliability and lifetime of products made with stabilized zirconia.
  • 12.
  • 13.
  • 14. • Zirconia may be in the form of blocks that are milled to create the frameworks (CAD/CAM). • Mostly, they are fabricated from a porous block, milled oversized by about 25%, and sintered to full density in a 4 - 6 hours cycle. • Alternatively, fully dense blocks are milled. However, this approach requires approximately 2 hours of milling time per unit whereas milling of the porous block necessitates only 30 to 45 minutes for a three-unit bridge.
  • 15. Properties of zirconia • Low thermal conductivity (20% that of alumina) • Chemically inert ant corrosion resistant • Flexural strength 900 Mpa • Fracture toughness 8-10 MPa · m1/2 • High fracture resistance • Wear of opposing dentition(Monolithic Zirconia) • Difficulty in adjusting occlusion
  • 16. Fracture toughness of zirconia • Fracture toughness of zirconia tends to increase with increasing grain size (0.9µm-1.4 µm). • There is a decrease in strength caused by very large grain size(1.8 µm) caused by premature phase transformation leading to microcracking
  • 17. Hydrothermal degradation of zirconia • Hydrothermal degradation of zirconia occurs between 200-400 ˚C . • Longer exposure times at oral temperature may also degrade zirconia leading to increased surface roughness,fragmanted grains and microcracks .
  • 18. Zirconia toughened alumina ZTA • 70-90% alumina • 10-20% zironia • Toughened by a stress-induced transformation mechanism of zirconia leading to compressive stresses within alumina. • The strength of alumina is doubled and toughness is increase 2-4 times .
  • 19.
  • 20. Methods of strengthening Dental ceramics Strengthening Methods Strengthening brittle materials Introduction of residual compressive stresses Ion strenghtening Thermal compatibility Interruption of crack propagation Incorporation of crystalline phase Heat treatment ceramming Methods of designing to Minimize tensile stress through design Avoid stress raisers
  • 21. 1.Strengthening of brittle materials a.Introduction of residual compressive stresses Ion strengthening • Replacing smaller ions by relatively larger ones • As a result crack growth from surface flaws is more difficult Thermal compatibilty • In PFM ,metals and porcelain are designed with a slight mismatch in COTE (metal slightly higher) • Metal contracts more on cooling • This leaves porcelain in residual compression
  • 22. 1.Strengthening of brittle materials b.Interruption of crack propagation Incorporation of crystalline phase • Tough crystaline material as alumina or leucite is added to galss in a particulate form,the glass is toughened and strengthened (Dispersion tougheneing) Heat treatment ceramming • A glass cerammic material is fabricated in vitreous or noncrystalline state and then converted to a crystalline state by heat treatment to induce partial devitrifaction • Crystalline particles,needles or plates formed during ceramming serve to interrupt cracks
  • 23. 2.Design of dental restorations to : a.Minimize tensile stress • In case of PFM ,metal copings act as the foundation. • The strong yet more ductile metal prevents the interior of porcelain portion of the crown from being subjected to tensile stresses. b.Avoid stress raisers • Sharp line angles in preparation should be removed. • Sharp line angles in coping surface should be avoided • Sudden changes in porcelain thickness should be avoided.