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• Dental ceramics are attractive because of their III. Types of Veneering Ceramics
bio compatibility, long-term color stability, chemical A. Feldspathic porcelains
durability, wear resistance, and ability to be formed 1. Ultralow- and low-fusing ceramics
into precise shapes, 2. Low-fusing specialty ceramics
• Nonmetallic, inorganic structures 3. Ceramic stains
• Contain compounds of oxygen with metallic or semi- 4. Ceramic glazes
metallic elements
• Crystal phase and silicate glass matrix phase D. I. Silicate Glass in Feldspathic Porcelains
Structure characterized by chains of (SiO4)4- A. Silica (SiO2) can exist in crystalline and noncrystalline
tetrahedra forms
B. Fused silica has a high-melting temperature due to the
covalent bonds between silica tetrahedra
Structure of Dental Ceramics C. Fluxes are added to reduce sintering temperature and
prevent alloy melting or deformation
• SiO4 tetrahedra linked by sharing corners
• Arranged as linked chains of tetrahedra II. Potassium and Sodium Feldspars
• Primary structural unit is the negatively charged A. Naturally occurring minerals used in dental porcelains
silicon-oxygen tetrahedron (SiO4)4- B. Potassium feldspar forms leucite and a glass phase during
• Covalent and ionic bonds in the structure firing, allowing porcelain particles to coalesce
C. Feldspar tendency to form leucite controls thermal
Feldspathic Veneering Porcelains expansion
• Alkali ions (sodium or potassium) bond to
III. Compositions of Veneering Ceramics
unbalanced oxygen ions
A. Similar to veneering aluminous porcelain core ceramics
• Alkali cations disrupt silicate chains and increase
with increased K2O and Na2O concentrations
thermal expansion
B. Specific concentrations of soda, potash, and leucite
• Crystalline particles (e.g., tetragonal leucite) increase
required for compatibility with metal coping
expansion coefficient
C. Opaque porcelains contain metallic oxide opacifiers to
• Potash feldspar and leucite are primary phase fields
conceal metal
in feldspathic veneering ceramics
IV. Thermal Properties and Considerations
CLASSIFICATION OF DENTAL CERAMICS
A. Veneering ceramics for metals have higher expansion
and contraction coefficients than ceramics for alumina or
zirconia
B. Nonessential repeated firings can lead to devitrification
and changes in thermal properties
C. Matching thermal properties of alloy and porcelain is
crucial to prevent chipping or cracking in clinical service
CERAMIC COMPOSITION
COPING DESIGN
• There are six features of importance to be considered
when designing the metal coping for an MCR:
1. Thickness of the porcelain veneer
2. Support of the porcelain veneer
3. Thickness of metal underlying and
adjoining the porcelain
4. Placement of occlusal and proximal
contacts
5. Extent of the area to be veneered for
porcelain
6. Design of the facial margin
BONDING MECHANISMS
• Four mechanisms have been described to explain the 1. Thickness of the porcelain veneer
bond between the ceramic veneer and the metal • The absolute minimum thickness of porcelain is 0.7
substructure: mm, and the desirable thickness is 1.0 to 1.5 mm.
1. Mechanical entrapment Extensions of porcelain beyond 2.0 mm are prone to
2. Compressive forces fracture even if these thick areas of porcelain are not
3. Van der Waals forces in areas of force concentration
4. Chemical bonding 2. Support of the porcelain veneer
• An evenly flowing convex contour of the veneering
Mechanical entrapment
area distributes stress best. Sharp angles and
• creates attachment by interlocking the ceramic with undercuts should be avoided.
microabrasions in the surface of the metal coping,
• An acute angle of metal at the metal porcelain
which are produced by finishing the metal with
interface is more likely to produce porcelain crazing
noncontaminating stones or disks and air abrasion
than an angle of 90 or 135 degrees
Compresive forces
• When the coefficient of thermal expansion of a
properly designed metal coping is slightly higher than
that of the porcelain veneered over it, compressive
forces develop. The slight difference in coefficients of
thermal expansion, or thermal contraction as is the
case during cooling, will cause the porcelain to draw 3. Thickness of metal underlying and adjoining the porcelain
toward the metal coping when the restoration cools • For adequate strength and rigidity, a noble metal
after firing coping should be at least 0.3 to 0.5 mm thick. 27 A
base metal alloy with a higher yield strength and
Van der Waals forces elevated melting temperature may be as thin as 0.2
• comprise an affinity based on a mutual attraction of mm. 28 The thickness of the coping may vary,
charged molecules. They contribute to bonding, but depending on the configuration of the preparation.
they are a minor force that is not as significant as was These values are only minimum thicknesses for
once though different alloy systems. The ultimate goal of achieving
a uniform thickness of approximately 1.0 mm of
porcelain will dictate the thickness of the metal
coping.
PORCELAIN ADDITION
Shade modification
• If the shade of a metal-ceramic crown is too dark (its
value too low or chroma too high), it is almost
impossible to lighten it by custom staining without
making the tooth appear too opaque. However, if it is
too light (its value too high or chroma too low), it can
be modified.
Chairside correction
• The simplest procedure is recontouring and
subsequently polishing modified areas.
• Excessive heat and vibration can initiate
microfractures that may lead to premature failure of
the porcelain
• fire small increments of porcelain such as for
perfecting proximal contacts, occlusal contacts,
pontic tissue contact areas, or other minor contour
additions