Investment materials
Dr Lekshmy AR
1st
year MDS
Contents
• Definitions
• Requirements of investment materials
• Gypsum-bonded investment
• Phosphate-bonded investment
• Silicate-bonded investment
• Implication of material science during casting
• Other investment materials
• Summary
• References
Investing : The process of covering or
enveloping, wholly or in part, an object such as a
denture, tooth, wax form, crown, etc., with a
suitable investment material before processing,
soldering, or casting (GPT 9)
Definitions
Dental casting investment : A material
consisting principally of an allotrope of silica and a
bonding Agent; the bonding substance may be
gypsum (for use in lower Casting temperatures)
or phosphates and silica (for use in higher
Casting temperatures) (GPT 9)
Requirements of an investment material
 Must reproduce precisely the details form of the wax pattern
 Must provide sufficient strength to withstand the heat of burnout and
the impact and the pressure of cast molten alloy
 Must maintain the integrity at higher temperatures and should not
decompose to give off gases
 Must expand sufficiently to compensate for the solidification
shrinkage of the alloy
 Easily manipulated and setting time should be less
 Should be inexpensive
 Biological safety Fundamentals
Fundamentals of fixed prosthodontics,
3rd
edi.Herbert T. Shillingburg
Composition
An investment is a mixture of three distinct types of materials
 Refractory material
 Binder material
 Additives.
Refractory material
It is usually a form of silicon dioxide, such as quartz, tridymite,
or cristobalite, or a mixture of these.
Binder material
As the refractory material alone do not form a coherent solid
mass, some kind of binder is needed.
Common binder used are:
1. α-calcium sulfate hemihydrate
2. Phosphate
3. Ethyl silicate
Other chemicals
• Sodium chloride, boric acid, potassium sulfate, graphite, copper
powder, or magnesium oxide are added in small quantities.
Classification
Types Uses
1 Gypsum bonded investment Gold alloy inlays, onlays,
FPD
2 Phosphate bonded investment Base metal alloys FPD &
metal ceramic alloys
3 Silica bonded investment Co-Ni alloys, base metal
alloy partial dentures.
Gypsum bonded investment material
 They are the mold materials used in the casting of
dental gold alloys with temperature below 7000
C.
 Used for conventional casting of gold alloy inlays,
onlays, crowns and fpd.
 ADA specification-2; divided them further into
• Type I- for casting inlays/crowns.
Mode of expansion: thermal
• Type II-for casting inlays/crowns
Mode of expansion : hygroscopic
• Type III-for partial dentures with gold alloys
Composition
Refractory
o Crystalline polymorphs of silica (quartz or cristobalite)
o 55-75%
o Silica is added to provide a refractory component during the
heating of the investment and to regulate the thermal expansion.
Binder
• Alpha hemi hydrate form of gypsum(25-45%)
• Strength of investment depends on amount of binder present.
Additives - (4-7%)
Used are
• Reducing agents
• Modifying chemicals
• Coloring matter
• Reducing agents : they reduce any metal oxides formed
on the metal by providing a non oxidizing atmosphere in
the mold when the alloy enters mold.
Eg– Copper
Modifying chemicals: They regulate setting expansion
and setting time and also prevent shrinkage of gypsum when
heated above 200ºC .
Eg– Boric acid,
Soluble salts of alkali or alkaline earth metals
Setting reaction
Theories to explain setting reaction
1.Colloidal theory
2.Hydration theory
3.Dissolution –precipitation theory
Among these dissolution-precipitation theory most
accepted
Dissolution of calcium sulfate hemihydrate
Formation of saturated solution of calcium sulfate
Aggregation of calcium sulfate dihydrate
Precipitation of dihydrate crystals
The crystallization of calcium sulfate dihydrate
Properties
1. Setting time
• According to ANSI/ADA Specification No. 2 for dental
inlay casting investment, the setting time should not be
shorter than 5 min or longer than 25 min.
• Usually, the modern inlay investments set initially in 9
to 18 min.
• Should allow sufficient time for mixing and investing
the pattern.
Factors controlling setting time
o Mixing time
o Water powder ratio
o Temperature
o Modifiers
2.Setting expansion
1. Normal setting expansion: the expansion takes
place when the material sets in air
2. Hygroscopic setting expansion: when setting occurs
under water.
3. Thermal expansion: when it is affected by heat
Purpose: enlarging the mold to compensate for the
casting shrinkage of the gold alloy
a) Normal Setting Expansion
• Liner dimensional change as the investment sets
• A mixture of silica and hemihydrate gypsum results setting
expansion greater than that of gypsum product used alone
• Silica particles interfere with the intermeshing and
interlocking of crystals resulting in outward thrust of
crystals resulting in expansion
• Maximum setting expansion – 0.5%
b) Hygroscopic setting expansion
 Greater in magnitude than NSE.
 The gypsum product is allowed to set in contact with
water for mold expansion.
 Curve A-NSE;
 Curve B-Hygroscopic expansion
 Water is added 5 min after beginning of the mixing
• The hygroscopic setting expansion may be 6 or more times
greater than the normal setting expansion of a dental
investment
• The increased amount of expansion is because the water
helps the outward growth of crystals
• The investment should be immersed in water before the initial
set is complete.
• ADA sp no 2 for such type 2 investments require minimum
setting expansion in water of 1.2% and maximum 2.2%.
Factors affecting expansion
 Composition: more finer silica particles -more HSE.
 α hemihydrate greater HSE than β hemihydrate.
 W:P ratio-lower W:P ratio-more HSE
 Spatulation: more mixing time- more HSE.
 Time of immersion: immerse in water before initial set more
expansion than immersion is delayed beyond the time of initial set.
 Confinement of the investment by the walls of the
container or the wax pattern reduces HSE.
 Added Water : HSE directly related to amount of water
added during the setting period until a maximum
expansion occurs.
 Shelf life: fresher investment-more HSE
c) Thermal setting expansion
• The thermal expansion is directly related to the amount and
type of silica present.
• Contraction of gypsum is balanced when quartz content
increases to 75%.
• Type 1 investments should have thermal expansion of not less
than1% and not greater than 1.6%.
• Type II investments should have thermal expansion of
between 0% to 0.6% at 500°C.
• Maximum thermal expansion should be attained at
temperature not higher than 700 degree centigrade
Factors affecting thermal expansion
• W/P ratio-more water less expansion
• Related to the amount and type of silica used
• Chemical modifiers : NaCl, KCl, LiCl increases TE
3.Setting contraction
• When an investment is cooled from 700°C, it contracts but
less than its original dimension.
• On reheating it expand thermally to the same maximum
reached before.
Precaution – Investment should not be heated a second time
because internal cracks may develop.
4.Compressive strength
• According to ADA sp no 2 the compressive strength should not
be less than 2.4mpa when tested 2 hr after setting
5.Fineness
• Surface roughness of the casting and setting time depend upon
the fineness of the material.
• Fine Silica- more hygroscopic expansion.
6.Porosity
• The material should be porous to allow escape of air from mold space
while casting.
• The common method of venting the mold is through the pores of the
investment.
Storage
• Should be stored in airtight and moisture proof
containers.
• Purchase in small quantities.
Phosphate bonded Investment material
• Most palladium and base metal alloys used for partial dentures
and porcelain fused to metal restorations have high melting
temperatures.
• They should be cast at a mold temperature higher than 700ºc.
• To withstand these high temperatures ,molds require
different types of binders such as phosphate compounds.
• They are used in construction of high melting temperature
dental alloys.
• Soldering and porcelain veneering
Types
ADA Sp No.42
Type 1
• For casting of inlays crowns and other fixed restorations
Type 2
• For casting of removable partial dentures
Composition
Refractory materials (Approximately 80%)
Silica in quartz , cristobalite or a mixture of two .
Purpose
• To provide high temperature thermal shock resistance
• To provide high thermal expansion.
Binder (<20%)
Magnesium oxide (base) and a phosphate (acid)
• Originally phosphoric acid was used but mono ammonium
phosphate has replaced it.
• It can be incorporated in powder form
Modifiers
• Carbon is often added -clean casting.
• Facilitates easy divesting of casting and mold.
• Generally added when casting alloy is gold.
• Not used with Ag-palladium alloys or base metal alloys as;
o palladium reacts with carbon at temperatures
above15040
C
o carbon embrittles the alloys.
It is available as two component systems
1. Powder which contains refractory materials, binders and
modifiers.
2. Aqueous solution stabilized with colloidal silica
Colloidal silica suspension facilitate greater expansion of the
investment which can compensate the greater casting
shrinkage of alloys used in Metal Ceramic & newer gold
alloys.
Setting reaction
• The chemical reaction that causes the investment to set and
harden is
NH4H2PO4 +MgO+5H2O→NH4MgPO4 +6H2O
• The product formed is predominantly colloidal multimolecular
(NH4MgPO4·6H2O)n aggregate around excess MgO and fillers.
Properties
• Compressive strength
o Type 1- 2.5 Mpa
o Type 2- 3 Mpa
• Thermal expansion
o 0.8% when 50:50 mixture of liquid and water
Working & setting time
o Temperature
Warmer the mix faster it sets
o The setting reaction also liberate the heat and
accelerates rate of setting
Mixing time
o Increased mixing time and mixing efficiency result
in faster set.
Surface Quality of cast metal
 Detail reproduction and surface smoothness of a metal-
ceramic gold alloy restoration cast in a phosphate
bonded investment were considered inferior to those
with gypsum-bonded investment.
 Due to improvement in technique and in composition of
material Phosphate bonded investments now approach
the surface quality or fineness of the gypsum
investments,
Advantages
 They have high fired strength.
 They also provide high setting and thermal expansion enough to
compensate cast metal shrinkage.
 3They can withstand temp more than 700°C
Disadvantage
• Rougher surfaces on casting.
• Difficult in divesting.
• Less porous than gypsum bonded investment .
Modifications
1. Phosphate bonded refractory cast for RPD
2. Investment for ceramics
Eg: Polyvest and VHT-whipmix
o Fine grained
o Working time 4-5 min
o Withstand repeated firing up to 12000
c
o Used with high expanding porcelains.
Casting
Investing procedure-common for both gypsum and Phosphate
investment
1. Mixing by-
1.Hand mixing
2.Vacuum mixing.
(In vacuum mixing-removes air bubbles, texture somewhat smoother
and better details reproduction)
• Excessive vibration should be avoided as-
o Causes solids in the investment to settle and may
lead to free water accumulation adjacent to wax
pattern
o Surface roughness
o May dislodge small pattern produce a miscast
3. Wax elimination and Heating
after investment set, approximately-1hr,it
is ready for burnout
Burnout temperature
• Gypsum investment
o 5000
C for hygroscopic technique
o 7000
C for thermal expansion technique
• Phosphate bonded investment
o Range from 7500
C to 10300
C depending on
the type of alloy
• The temperature setting is more critical with gypsum-
bonded investments than for the phosphate type because
the gypsum investments are more prone to investment
decomposition.
• As temperature rises above 7000
C ,calcium sulfate reduce
as following reaction-
CaSO4 + 4C CaS + 4CO
3CaSO4 + CaS 4CaO+ 4SO2
Heating in burnout furnace
• For gypsum bonded investment
o The molds are usually placed in a furnace at room
temperature, slowly heated to 650 °C to 700 °C in 60
minutes, and held for 15 to 30 minutes at the upper
temperature.
• For phosphate bonded investment
o The heating rate is usually slow to 315 °C and is quite
rapid thereafter, reaching completion after a hold at the
upper temperature for 30 minutes.
Ethyl silicate bonded Investments
• Though losing popularity because of the more complicated and
time consuming procedures, still used in the construction of high
fusing base metal partial denture alloy.
Composition
• Refractory material – Silica
• Binder –Silica gel that reverts to silica
(cristobalite) on heating.
• Modifier – Magnesium oxide (strengthen the gel)
Ammonium chloride - accelerator
Binder
 Ethyl silicate
o Colloidal silicic acid is formed by hydrolysing ethyl
silicate in presence of HCl, ethyl alcohol& water.
Si(OC2H5)+4H2O Si(OH)4+4C2H5OH
• It is then mixed with quartz or cristobalite and magnesium oxide
(alkaline).
• Coherent gel of polysilicic acid formed(accompanied by a setting
shrinkage) ,dried at temp 168°C, loses alcohol & water to form
concentrated hard gel .
• Volumetric contraction during drying is known as green shrinkage.
• As the gelation process is slow and time consuming , amines are
added to ethyl silicate- hydrolysis and gelation occurs
simultaneously.
It is supplied as a powder and liquid
 Powder consists of refractory particles of silica and
glasses along with the magnesium oxide and some
other refractory oxides in minor amounts
 Liquid contains stabilized alcohol solution of silica
gel
Manipulation
• The powder is added to hydrolysed ethyl silicate liquid, mixed
quickly and vibrated into a mold , that has an extra collar to
increase the height.
• The mold is placed on a vibrator that has a tamping action
• This allows the heavier particles to settle while the excess liquid
and some of the finer particles rise to the top .
• In about 30 minutes the accelerator in the powder hardens the
settled part, and the excess is poured off (to avoid crack
formation).
• The liquid powder ratio in settled part is greatly reduced and
the setting shrinkage is reduced to 0.1%
• Can be used for higher temp castings (1090°C-
1180°C) and compactible with higher fusing alloys.
• Care should be taken while handling and burnout as
inflammable alcohol is given off.
Disadvantage
• Non porous material.
• Complicated manipulation
• Cannot be used for titanium and its
alloys as silica can oxidize titanium or its
alloys easily.
Other investment materials
Soldering investment
Divestment materials
Investment material for titanium alloys
 Investments for all ceramic restoration
Soldering investment
• ANSI/ADA Specification No. 93 (IS0 11244) for dental
brazing investments defines two types of investment:
o Type 1: Gypsum-bonded dental brazing
investments
o Type 2: Phosphate-bonded dental brazing
investments
Soldering investment differ from casting investment by
• lower setting and thermal expansion
• most often ingredients do not have as fine particle as
casting investment
Uses
Type 1- for soldering of low melting alloys
Type 2 - for soldering of high melting alloys
Divestment
• Die stone and investment combination.
• These mixed with colloidal silica liquid
• The die is made from this mix and the wax pattern is then
constructed on it.
• The whole complex is then invested in a mixture of divestment
and water
• This combination used to compensate distortion of wax pattern
of long span bridges or RPD frameworks during removal from
die.
Newer investments for casting titanium based alloys
Problems with conventional investment materials-
• Molten titanium is highly reactive with the oxygen and is capable of
reducing some of the oxides commonly found in the investment.
• Titanium can also dissolve residual oxygen, nitrogen, and carbon from
the investments.
• These elements can also embrittle titanium in the solid state.
Objective for a titanium investment
• To reduce breakdown of the investment
• To reduce contamination of the titanium – refractory
materials that are less easily reduced by titanium
should be used
Investments used for casting Titanium alloy
Silica based investment
Magnesia based investment
Zirconia based investment
Alumina based investment
Resin based calcium investment
Conclusion
• Due to increase in the use of the higher melting alloys,
the use of phosphate bonded investment materials
increased.
• Gypsum bonded investment cannot withstand
temperature higher than 7000
C and it can be used only
with conventional gold alloys.
• The complex procedures limited the use of silicate
bonded investments.
• Due to highly reactive of titanium with the oxygen in
the mold cavity , newer investment materials are
developed.
• Gypsum bonded investment
(7000
C)
• Phosphate bonded investment
(700-10300
C)
• Silica bonded investments
(1090-11800
C)
• Mold for gold casting alloys
• Mold for base metal and gold
casting alloys, cast ceramic and
glasses
• Mold for base metal casting
alloys
References-
• Phillips Science of Dental material, 11th edition
• Restorative Dental materials, Robert G. Craig.11th
edition
• Fundamentals of fixed prosthodontics,3rd
edi.
Herbert T. Shillingburg

Investment materials .pptx

  • 1.
  • 2.
    Contents • Definitions • Requirementsof investment materials • Gypsum-bonded investment • Phosphate-bonded investment • Silicate-bonded investment • Implication of material science during casting • Other investment materials • Summary • References
  • 3.
    Investing : Theprocess of covering or enveloping, wholly or in part, an object such as a denture, tooth, wax form, crown, etc., with a suitable investment material before processing, soldering, or casting (GPT 9) Definitions Dental casting investment : A material consisting principally of an allotrope of silica and a bonding Agent; the bonding substance may be gypsum (for use in lower Casting temperatures) or phosphates and silica (for use in higher Casting temperatures) (GPT 9)
  • 4.
    Requirements of aninvestment material  Must reproduce precisely the details form of the wax pattern  Must provide sufficient strength to withstand the heat of burnout and the impact and the pressure of cast molten alloy  Must maintain the integrity at higher temperatures and should not decompose to give off gases  Must expand sufficiently to compensate for the solidification shrinkage of the alloy  Easily manipulated and setting time should be less  Should be inexpensive  Biological safety Fundamentals Fundamentals of fixed prosthodontics, 3rd edi.Herbert T. Shillingburg
  • 5.
    Composition An investment isa mixture of three distinct types of materials  Refractory material  Binder material  Additives.
  • 6.
    Refractory material It isusually a form of silicon dioxide, such as quartz, tridymite, or cristobalite, or a mixture of these. Binder material As the refractory material alone do not form a coherent solid mass, some kind of binder is needed.
  • 7.
    Common binder usedare: 1. α-calcium sulfate hemihydrate 2. Phosphate 3. Ethyl silicate
  • 8.
    Other chemicals • Sodiumchloride, boric acid, potassium sulfate, graphite, copper powder, or magnesium oxide are added in small quantities.
  • 9.
    Classification Types Uses 1 Gypsumbonded investment Gold alloy inlays, onlays, FPD 2 Phosphate bonded investment Base metal alloys FPD & metal ceramic alloys 3 Silica bonded investment Co-Ni alloys, base metal alloy partial dentures.
  • 10.
    Gypsum bonded investmentmaterial  They are the mold materials used in the casting of dental gold alloys with temperature below 7000 C.  Used for conventional casting of gold alloy inlays, onlays, crowns and fpd.
  • 11.
     ADA specification-2;divided them further into • Type I- for casting inlays/crowns. Mode of expansion: thermal • Type II-for casting inlays/crowns Mode of expansion : hygroscopic • Type III-for partial dentures with gold alloys
  • 12.
    Composition Refractory o Crystalline polymorphsof silica (quartz or cristobalite) o 55-75% o Silica is added to provide a refractory component during the heating of the investment and to regulate the thermal expansion.
  • 13.
    Binder • Alpha hemihydrate form of gypsum(25-45%) • Strength of investment depends on amount of binder present.
  • 14.
    Additives - (4-7%) Usedare • Reducing agents • Modifying chemicals • Coloring matter • Reducing agents : they reduce any metal oxides formed on the metal by providing a non oxidizing atmosphere in the mold when the alloy enters mold. Eg– Copper
  • 15.
    Modifying chemicals: Theyregulate setting expansion and setting time and also prevent shrinkage of gypsum when heated above 200ºC . Eg– Boric acid, Soluble salts of alkali or alkaline earth metals
  • 16.
    Setting reaction Theories toexplain setting reaction 1.Colloidal theory 2.Hydration theory 3.Dissolution –precipitation theory Among these dissolution-precipitation theory most accepted
  • 17.
    Dissolution of calciumsulfate hemihydrate Formation of saturated solution of calcium sulfate Aggregation of calcium sulfate dihydrate Precipitation of dihydrate crystals The crystallization of calcium sulfate dihydrate
  • 18.
    Properties 1. Setting time •According to ANSI/ADA Specification No. 2 for dental inlay casting investment, the setting time should not be shorter than 5 min or longer than 25 min. • Usually, the modern inlay investments set initially in 9 to 18 min. • Should allow sufficient time for mixing and investing the pattern.
  • 19.
    Factors controlling settingtime o Mixing time o Water powder ratio o Temperature o Modifiers
  • 20.
    2.Setting expansion 1. Normalsetting expansion: the expansion takes place when the material sets in air 2. Hygroscopic setting expansion: when setting occurs under water. 3. Thermal expansion: when it is affected by heat Purpose: enlarging the mold to compensate for the casting shrinkage of the gold alloy
  • 21.
    a) Normal SettingExpansion • Liner dimensional change as the investment sets • A mixture of silica and hemihydrate gypsum results setting expansion greater than that of gypsum product used alone • Silica particles interfere with the intermeshing and interlocking of crystals resulting in outward thrust of crystals resulting in expansion • Maximum setting expansion – 0.5%
  • 22.
    b) Hygroscopic settingexpansion  Greater in magnitude than NSE.  The gypsum product is allowed to set in contact with water for mold expansion.  Curve A-NSE;  Curve B-Hygroscopic expansion  Water is added 5 min after beginning of the mixing
  • 23.
    • The hygroscopicsetting expansion may be 6 or more times greater than the normal setting expansion of a dental investment • The increased amount of expansion is because the water helps the outward growth of crystals • The investment should be immersed in water before the initial set is complete. • ADA sp no 2 for such type 2 investments require minimum setting expansion in water of 1.2% and maximum 2.2%.
  • 24.
    Factors affecting expansion Composition: more finer silica particles -more HSE.  α hemihydrate greater HSE than β hemihydrate.  W:P ratio-lower W:P ratio-more HSE  Spatulation: more mixing time- more HSE.  Time of immersion: immerse in water before initial set more expansion than immersion is delayed beyond the time of initial set.
  • 25.
     Confinement ofthe investment by the walls of the container or the wax pattern reduces HSE.  Added Water : HSE directly related to amount of water added during the setting period until a maximum expansion occurs.  Shelf life: fresher investment-more HSE
  • 26.
    c) Thermal settingexpansion • The thermal expansion is directly related to the amount and type of silica present. • Contraction of gypsum is balanced when quartz content increases to 75%. • Type 1 investments should have thermal expansion of not less than1% and not greater than 1.6%.
  • 27.
    • Type IIinvestments should have thermal expansion of between 0% to 0.6% at 500°C. • Maximum thermal expansion should be attained at temperature not higher than 700 degree centigrade Factors affecting thermal expansion • W/P ratio-more water less expansion • Related to the amount and type of silica used • Chemical modifiers : NaCl, KCl, LiCl increases TE
  • 28.
    3.Setting contraction • Whenan investment is cooled from 700°C, it contracts but less than its original dimension. • On reheating it expand thermally to the same maximum reached before. Precaution – Investment should not be heated a second time because internal cracks may develop.
  • 29.
    4.Compressive strength • Accordingto ADA sp no 2 the compressive strength should not be less than 2.4mpa when tested 2 hr after setting 5.Fineness • Surface roughness of the casting and setting time depend upon the fineness of the material. • Fine Silica- more hygroscopic expansion.
  • 30.
    6.Porosity • The materialshould be porous to allow escape of air from mold space while casting. • The common method of venting the mold is through the pores of the investment.
  • 31.
    Storage • Should bestored in airtight and moisture proof containers. • Purchase in small quantities.
  • 32.
    Phosphate bonded Investmentmaterial • Most palladium and base metal alloys used for partial dentures and porcelain fused to metal restorations have high melting temperatures. • They should be cast at a mold temperature higher than 700ºc.
  • 33.
    • To withstandthese high temperatures ,molds require different types of binders such as phosphate compounds. • They are used in construction of high melting temperature dental alloys. • Soldering and porcelain veneering
  • 34.
    Types ADA Sp No.42 Type1 • For casting of inlays crowns and other fixed restorations Type 2 • For casting of removable partial dentures
  • 35.
    Composition Refractory materials (Approximately80%) Silica in quartz , cristobalite or a mixture of two . Purpose • To provide high temperature thermal shock resistance • To provide high thermal expansion.
  • 36.
    Binder (<20%) Magnesium oxide(base) and a phosphate (acid) • Originally phosphoric acid was used but mono ammonium phosphate has replaced it. • It can be incorporated in powder form
  • 37.
    Modifiers • Carbon isoften added -clean casting. • Facilitates easy divesting of casting and mold. • Generally added when casting alloy is gold. • Not used with Ag-palladium alloys or base metal alloys as; o palladium reacts with carbon at temperatures above15040 C o carbon embrittles the alloys.
  • 38.
    It is availableas two component systems 1. Powder which contains refractory materials, binders and modifiers. 2. Aqueous solution stabilized with colloidal silica Colloidal silica suspension facilitate greater expansion of the investment which can compensate the greater casting shrinkage of alloys used in Metal Ceramic & newer gold alloys.
  • 39.
    Setting reaction • Thechemical reaction that causes the investment to set and harden is NH4H2PO4 +MgO+5H2O→NH4MgPO4 +6H2O • The product formed is predominantly colloidal multimolecular (NH4MgPO4·6H2O)n aggregate around excess MgO and fillers.
  • 40.
    Properties • Compressive strength oType 1- 2.5 Mpa o Type 2- 3 Mpa • Thermal expansion o 0.8% when 50:50 mixture of liquid and water
  • 41.
    Working & settingtime o Temperature Warmer the mix faster it sets o The setting reaction also liberate the heat and accelerates rate of setting Mixing time o Increased mixing time and mixing efficiency result in faster set.
  • 42.
    Surface Quality ofcast metal  Detail reproduction and surface smoothness of a metal- ceramic gold alloy restoration cast in a phosphate bonded investment were considered inferior to those with gypsum-bonded investment.  Due to improvement in technique and in composition of material Phosphate bonded investments now approach the surface quality or fineness of the gypsum investments,
  • 43.
    Advantages  They havehigh fired strength.  They also provide high setting and thermal expansion enough to compensate cast metal shrinkage.  3They can withstand temp more than 700°C
  • 44.
    Disadvantage • Rougher surfaceson casting. • Difficult in divesting. • Less porous than gypsum bonded investment .
  • 45.
    Modifications 1. Phosphate bondedrefractory cast for RPD 2. Investment for ceramics Eg: Polyvest and VHT-whipmix o Fine grained o Working time 4-5 min o Withstand repeated firing up to 12000 c o Used with high expanding porcelains.
  • 46.
    Casting Investing procedure-common forboth gypsum and Phosphate investment 1. Mixing by- 1.Hand mixing 2.Vacuum mixing. (In vacuum mixing-removes air bubbles, texture somewhat smoother and better details reproduction)
  • 47.
    • Excessive vibrationshould be avoided as- o Causes solids in the investment to settle and may lead to free water accumulation adjacent to wax pattern o Surface roughness o May dislodge small pattern produce a miscast
  • 48.
    3. Wax eliminationand Heating after investment set, approximately-1hr,it is ready for burnout Burnout temperature • Gypsum investment o 5000 C for hygroscopic technique o 7000 C for thermal expansion technique • Phosphate bonded investment o Range from 7500 C to 10300 C depending on the type of alloy
  • 49.
    • The temperaturesetting is more critical with gypsum- bonded investments than for the phosphate type because the gypsum investments are more prone to investment decomposition. • As temperature rises above 7000 C ,calcium sulfate reduce as following reaction- CaSO4 + 4C CaS + 4CO 3CaSO4 + CaS 4CaO+ 4SO2
  • 50.
    Heating in burnoutfurnace • For gypsum bonded investment o The molds are usually placed in a furnace at room temperature, slowly heated to 650 °C to 700 °C in 60 minutes, and held for 15 to 30 minutes at the upper temperature. • For phosphate bonded investment o The heating rate is usually slow to 315 °C and is quite rapid thereafter, reaching completion after a hold at the upper temperature for 30 minutes.
  • 52.
    Ethyl silicate bondedInvestments • Though losing popularity because of the more complicated and time consuming procedures, still used in the construction of high fusing base metal partial denture alloy.
  • 53.
    Composition • Refractory material– Silica • Binder –Silica gel that reverts to silica (cristobalite) on heating. • Modifier – Magnesium oxide (strengthen the gel) Ammonium chloride - accelerator
  • 54.
    Binder  Ethyl silicate oColloidal silicic acid is formed by hydrolysing ethyl silicate in presence of HCl, ethyl alcohol& water. Si(OC2H5)+4H2O Si(OH)4+4C2H5OH
  • 55.
    • It isthen mixed with quartz or cristobalite and magnesium oxide (alkaline). • Coherent gel of polysilicic acid formed(accompanied by a setting shrinkage) ,dried at temp 168°C, loses alcohol & water to form concentrated hard gel . • Volumetric contraction during drying is known as green shrinkage. • As the gelation process is slow and time consuming , amines are added to ethyl silicate- hydrolysis and gelation occurs simultaneously.
  • 56.
    It is suppliedas a powder and liquid  Powder consists of refractory particles of silica and glasses along with the magnesium oxide and some other refractory oxides in minor amounts  Liquid contains stabilized alcohol solution of silica gel
  • 57.
    Manipulation • The powderis added to hydrolysed ethyl silicate liquid, mixed quickly and vibrated into a mold , that has an extra collar to increase the height. • The mold is placed on a vibrator that has a tamping action • This allows the heavier particles to settle while the excess liquid and some of the finer particles rise to the top .
  • 58.
    • In about30 minutes the accelerator in the powder hardens the settled part, and the excess is poured off (to avoid crack formation). • The liquid powder ratio in settled part is greatly reduced and the setting shrinkage is reduced to 0.1%
  • 59.
    • Can beused for higher temp castings (1090°C- 1180°C) and compactible with higher fusing alloys. • Care should be taken while handling and burnout as inflammable alcohol is given off.
  • 60.
    Disadvantage • Non porousmaterial. • Complicated manipulation • Cannot be used for titanium and its alloys as silica can oxidize titanium or its alloys easily.
  • 61.
    Other investment materials Solderinginvestment Divestment materials Investment material for titanium alloys  Investments for all ceramic restoration
  • 62.
    Soldering investment • ANSI/ADASpecification No. 93 (IS0 11244) for dental brazing investments defines two types of investment: o Type 1: Gypsum-bonded dental brazing investments o Type 2: Phosphate-bonded dental brazing investments
  • 63.
    Soldering investment differfrom casting investment by • lower setting and thermal expansion • most often ingredients do not have as fine particle as casting investment Uses Type 1- for soldering of low melting alloys Type 2 - for soldering of high melting alloys
  • 64.
    Divestment • Die stoneand investment combination. • These mixed with colloidal silica liquid • The die is made from this mix and the wax pattern is then constructed on it. • The whole complex is then invested in a mixture of divestment and water • This combination used to compensate distortion of wax pattern of long span bridges or RPD frameworks during removal from die.
  • 65.
    Newer investments forcasting titanium based alloys Problems with conventional investment materials- • Molten titanium is highly reactive with the oxygen and is capable of reducing some of the oxides commonly found in the investment. • Titanium can also dissolve residual oxygen, nitrogen, and carbon from the investments. • These elements can also embrittle titanium in the solid state.
  • 66.
    Objective for atitanium investment • To reduce breakdown of the investment • To reduce contamination of the titanium – refractory materials that are less easily reduced by titanium should be used
  • 67.
    Investments used forcasting Titanium alloy Silica based investment Magnesia based investment Zirconia based investment Alumina based investment Resin based calcium investment
  • 68.
    Conclusion • Due toincrease in the use of the higher melting alloys, the use of phosphate bonded investment materials increased. • Gypsum bonded investment cannot withstand temperature higher than 7000 C and it can be used only with conventional gold alloys. • The complex procedures limited the use of silicate bonded investments. • Due to highly reactive of titanium with the oxygen in the mold cavity , newer investment materials are developed.
  • 69.
    • Gypsum bondedinvestment (7000 C) • Phosphate bonded investment (700-10300 C) • Silica bonded investments (1090-11800 C) • Mold for gold casting alloys • Mold for base metal and gold casting alloys, cast ceramic and glasses • Mold for base metal casting alloys
  • 70.
    References- • Phillips Scienceof Dental material, 11th edition • Restorative Dental materials, Robert G. Craig.11th edition • Fundamentals of fixed prosthodontics,3rd edi. Herbert T. Shillingburg