CA1251305A - Transparent ceramic surface layer for a ceramo- metallic dental reconstruction - Google Patents

Transparent ceramic surface layer for a ceramo- metallic dental reconstruction

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Publication number
CA1251305A
CA1251305A CA000474153A CA474153A CA1251305A CA 1251305 A CA1251305 A CA 1251305A CA 000474153 A CA000474153 A CA 000474153A CA 474153 A CA474153 A CA 474153A CA 1251305 A CA1251305 A CA 1251305A
Authority
CA
Canada
Prior art keywords
weight
particles
mixture
glass frits
ceramic layer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
CA000474153A
Other languages
French (fr)
Inventor
Michel Heurtaux
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Suissor SA
Original Assignee
Suissor SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Suissor SA filed Critical Suissor SA
Application granted granted Critical
Publication of CA1251305A publication Critical patent/CA1251305A/en
Expired legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K6/00Preparations for dentistry
    • A61K6/15Compositions characterised by their physical properties
    • A61K6/16Refractive index
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K6/00Preparations for dentistry
    • A61K6/15Compositions characterised by their physical properties
    • A61K6/17Particle size
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K6/00Preparations for dentistry
    • A61K6/20Protective coatings for natural or artificial teeth, e.g. sealings, dye coatings or varnish
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K6/00Preparations for dentistry
    • A61K6/80Preparations for artificial teeth, for filling teeth or for capping teeth
    • A61K6/802Preparations for artificial teeth, for filling teeth or for capping teeth comprising ceramics
    • A61K6/827Leucite
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K6/00Preparations for dentistry
    • A61K6/80Preparations for artificial teeth, for filling teeth or for capping teeth
    • A61K6/831Preparations for artificial teeth, for filling teeth or for capping teeth comprising non-metallic elements or compounds thereof, e.g. carbon
    • A61K6/833Glass-ceramic composites
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K6/00Preparations for dentistry
    • A61K6/80Preparations for artificial teeth, for filling teeth or for capping teeth
    • A61K6/84Preparations for artificial teeth, for filling teeth or for capping teeth comprising metals or alloys

Abstract

PATENT

TRANSPARENT CERAMIC SURFACE LAYER FOR A CERAMO-METALLIC
DENTAL RECONSTRUCTION

SUISSOR S.A.

Inventor: Michel HEURTAUX

ABSTRACT
The present invention relates to a transparent ceramic surface layer of a ceramo-metallic dental recon-struction.
The transparent ceramic surface layer of a ceramo-metallic dental reconstruction is produced from a mixture containing at least two separate glass frits.
Preferably, the first glass frit is fusible and does not devitrify, and the second glass frit is more refractory and devitrifies partially to leucite. In addition, particle size can be less than 65 µm to improve the properties with respect to shrinkage.

Description

:~2~

The present invention relates to the technlcal field oF ceramo-metallic dental recons-tructions. More par-ticularly, it relates to the composition of the ceramic glass employed to form the transparent surface layer of a dental reconstruction such as crowns, inlays, bridges, and the like.
This type of dental reconstruc-tion is usually produced from a series of ceramic layers coa-ted on a metal coping, deposited, for example, on the stump of a tooth reduced after shaping with a drill.
This series of ceramic layers consists of a basal opacifying layer, two intermediate layers known under the terms of "dentine" and "incisal" and a transparent surface layer intended to resemble the gleam of the enamel of the natural tooth.
The subject of the present invention is aimed precisely at producing this last transparent surface layer.
In the present state of the art no ceramic layer is available which is endowed with a perfect translucency comparable to that of a glass pane. A really translucent ceramic surface layer would enable the user -to give -the prosthesis the esthetic appearance of a natural -tooth.
The present invention improves the quality of transparent ceramic layers of this type.
In accordance with the present invention, the ceramic layer is produced From a mixture containing at least two separate glass frits, namely:
approximately 90 % by weight of a first glass frit which is fusible and does not devitrify, and ~$

approximately 10 % by weight of a second glass frit which is more refractory and devitrifies partially to leucite.
Other features and advantages of the present invention will become apparent from the reading of the detailed description which follows, particularly relying on an illustrative example of practical implementation.
The transparent ceramic layer in a preferred form has expansion co-efficients which are stable and match all the precious or base alloys.
The glass frit employed is produced by mixing two separate glasses, one fusible and non-devitrifying, the other slightly more refractory and devitrifying partially to leucite, a mineral with high thermal expansion.
The first glass frit, which is fusible and does not devitrify 9 is employed as such. In contrast, the second glass frit is devitrified, for example, for approxima-tely 12 hours at a temperature of the order of 900C. During this thermal devitrifying treatment, an in situ crys-tallization phenomenon makes its appearance in a conventional manner.
It will also be noted that, during successive bakings, the fusible glass, at the limit of saturation with leucite, does not dissolve the leuci-te in the second glass and consequently its proportion remains cons-tant. In this way, a stable expansion is produced.
The hardness of the transparent ceramic layer can also be reduced by an increase in the percentage of fluxes, favoring Na20. The ceramic layer is formed from a ,~ , 36)~

mixture of two glass frits containing, in to-tal, from approximately 20 to approxima-tely 30 % by weight of fluxes, among which soda Na20 is present in a proportion of approximately 7 to approximately 8 % by weight.
The following overall composition of transparent ceramic layers produces satisfactory results in practice and is given below by way of an illustrative example.
SiO2 59 to 59.5 % by weight A1203 15 to 16 % by weight CaO 0.5 to 1.5 % by weight MgO O to 0.2 % by weight K20 11 to 13 % by weight Na20 7 to 8 % by weight B203 2.5 to 3.5 % by weight BaO O to 3 % by weight CaF2 0.5 to 3 % by weight TiO2 0.2 to 0.5 % by weight The ceramic layers according to the invention have also been adapted so as to be capable of avoiding any background coloring phenomenon due to the metal substrates. These metal substrates are usually made from an alloy of various metals, among which silver is, in particular, responsible for such a background coloring. In fact, the Ag~-~ ion migrates fairly readily in the ceramic and causes a greenish yellow coloring when reduced to the metal s-tate. It is precisely to avoid a phenomenon o-F this type that approximately 0.2 % by weight of cerium oxide CeO2 7 which is an active oxidizing agent which keeps the silver in the non-coloring oxide state 9 is added to the ~, ~ 2513~

mixtures of glass frits according to the invention. This cerium oxide is added after the grinding operation which produces the glass frit. The glass frits are obtained in a conventional manner by melting and homogenizing a powdered mixture of the basic components required for producing the abovementioned compositions.
To reduce shrinkage during the baking, the particle size distribution of the mixture of -the two glass frits has been adjusted as a result of the following observation. The voidage of a population of large particles (40 to 65 microns) is of the order of 40 %. By introducing particles of medium size (12 to 40 microns) in a proportion of approximately 5û % by weight relative to the large particles, the voidage drops to approximately 20 %. Lastly, when particles of much smaller sizes (below 5 microns) are added, the voidage becomes still smaller.
Consequently, this results in a lower shrinkage on baking.
A particle size distribution of this type also makes it possible to obtain better plasticity of the paste at the time of its use.
In order to produce a glass frit according to the invention, intended for producing a transparent surface layer, it is thus desirable to make use of a particle size distribution of the following type:
40 to 65~ ...... 40 to 50 % of the particles 12 to 40 ~ ..... 30 to 35 % of the particles ~ 12~u ......... 15 to 30 % of the particles.
Glass frits required for the production of transparent ceramic surFace layers are presented in the . ' ~ :, 3~S

form of a paste ready for use and intended to facilitate the work of the user whlle making it possible to achieve a saving in active product. Such frits are presented in -the form of a paste containing a suitable quantity of a plas-ticizer~ so as to enable them -to be packaged in a tube or a dispenser for paste of the aerosol type.
A typical example of formulation of glass frits according to the invention, packaged in an aerosol dispenser, is given below:
100 parts by weight of active products, 30 to ~0 parts by weight of plasticizer, 100 parts by weigh-t of a propellant agent 7 such as a Freon .
Qccording to a particular embodiment of glass frits of this type, the plasticizer is preferably chosen from diethylene glycol diethyl ether and propylene glycol methyl ether.
Although various preferred embodiments of the present invention have been described herein in detail, it will be appreciated by those skilled in the art, that variations may be made thereto without departing from the spirit of the invention or -the scope of the appended claims.

Claims (12)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. Transparent ceramic surface layer of a ceramo-metallic dental reconstruction, which is produced from a mixture containing at least two separate glass frits, namely:
about 90% of a first glass frit which is fusible and does not devitrify, and about 10% of a second glass frit which is more refractory and devitrifies partially to leucite;
said glass frits having a particle size of less than about 65 µm, said mixture of glass frits containing from approximately 20 to approximately 30 % by weight of fluxes in which approximately 7 to approximately 8 % of Na2O by weight is present.
2. Ceramic layer as claimed in claim 17 in which the second glass frit is devitrified for approximately 12 hours at a temperature of the order of 900°C, before being mixed.
3. Ceramic layer as claimed in claim 1 or 2, which corresponds to the following overall composition:
SiO2 59 to 59.5 % by weight Al2O3 15 to 16 % by weight CaO 0.5 to 1.5 % by weight MgO 0 to 0.2 % by weight K2O 11 to 13 % by weight Na2O 7 to 8 % by weight B2O3 2.5 to 3.5 % by weight BaO 0 to 3 % by weight CaF2 0.5 to 3 % by weight TiO2 0.2 to 0.5 % by weight.
4. Ceramic layer as claimed in claim 1, which corresponds to the following overall composition:
SiO2 59 to 59.5 % by weight Al2O3 15 to 16 % by weight CaO 0.5 to 1.5 % by weight MgO 0 to 0.2 % by weight K2O 11 to 13 % by weight Na2O 7 to 8 % by weight B2O3 2.5 to 3.5 % by weight BaO 0 to 3 % by weight CaF2 0.5 to 3 % by weight TiO2 0.2 to 0.5 % by weight.
5. Ceramic layer as claimed in claim 1 or 2, in which the mixture of the two glass frits has a particle size distribution of the following type:
40 to 65 µ 40 to 50 % of the particles 12 to 40 µ 30 to 35 % of the particles < 12 µ 15 to 30 % of the particles.
6. Ceramic layer as claimed in claim 4, in which the mixture of the two glass frits has a particle size distribution of the following type:
40 to 65 µ 40 to 50 % of the particles 12 to 40 µ 30 to 35 % of the particles < 12 µ 15 to 30 % of the particles.
7. Ceramic layer as claimed in claim 1 or 2, in which the mixture of glass frits has a particle size distribution of the following type:
40 to 65 µ 40 to 50 % of the particles 12 to 40 µ 30 to 35 % of the particles < 12 µ 15 to 30 % of the particles which corresponds to the following overall composition:
SiO2 59 to 59.5 % by weight Al2O3 15 to 16 % by weight CaO 0.5 to 1.5 % by weight MgO 0 to 0.2 % by weight K2O 11 to 13 % by weight Na2O 7 to 8 % by weight B2O3 2.5 to 3.5 % by weight BaO 0 to 3 % by weight CaF2 0.5 to 3 % by weight TiO2 0.2 to 0.5 % by weight.
8. Glass frits required for the production of a ceramic layer as claimed in claim 1, 2 or 4, which are presented in the form of a paste ready for use containing a suitable quantity of a plasticizer, and suitable for being packaged in a tube or a dispenser for paste of the aerosol type.
9. Glass frits required for the production of a ceramic layer as claimed in claim 1 or 2, which are presented in the form of a paste ready for use containing a suitable quantity of a plasticizer, and suitable for being packaged in a tube or a dispenser for paste of the aerosol type, in which the plasticizer is chosen from diethylene glycol diethyl ether and propylene glycol methyl ether.
10. A transparent ceramic surface layer of a ceramo-metallic dental reconstruction, which is produced from a mixture containing at least two separate glass frits, namely, said mixture having the following overall composition:
SiO2 59 to 59.5 % by weight Al2O3 15 to 16 % by weight CaO 0.5 to 1.5 % by weight MgO 0 to 0.2 % by weight K2O 11 to 13 % by weight Na2O 7 to 8 % by weight B2O3 2.5 to 3.5 % by weight BaO 0 to 3 % by weight CaF2 0.5 to 3 % by weight and particles of said mixture having a size less than 65 µm.
11. A ceramic layer according to claim 10, in which the mixture of the two glass frits has a particle size distribution of the following type:
40 to 65 µ 40 to 50 % of the particles
12 to 40 µ 30 to 35 % of the particles < 12 µ 15 to 30 % of the particles.
CA000474153A 1984-02-15 1985-02-13 Transparent ceramic surface layer for a ceramo- metallic dental reconstruction Expired CA1251305A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR84/02297 1984-02-15
FR8402297A FR2559386B1 (en) 1984-02-15 1984-02-15 TRANSPARENT SURFACE CERAMIC LAYER OF A DENTAL CERAMO-METALLIC RECONSTITUTION

Publications (1)

Publication Number Publication Date
CA1251305A true CA1251305A (en) 1989-03-21

Family

ID=9301068

Family Applications (1)

Application Number Title Priority Date Filing Date
CA000474153A Expired CA1251305A (en) 1984-02-15 1985-02-13 Transparent ceramic surface layer for a ceramo- metallic dental reconstruction

Country Status (8)

Country Link
EP (1) EP0152338B1 (en)
JP (1) JPS60195033A (en)
AT (1) ATE44455T1 (en)
CA (1) CA1251305A (en)
DE (1) DE3571390D1 (en)
DK (1) DK69385A (en)
ES (1) ES8601678A1 (en)
FR (1) FR2559386B1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0631995A1 (en) 1993-06-24 1995-01-04 Dentsply GmbH Dental prosthesis
WO2011098115A1 (en) * 2010-02-09 2011-08-18 Vita Zahnfabrik H. Rauter Gmbh & Co. Kg A process for improving the stability of yttrium stabilised zirconia for dental restorations
US10391671B2 (en) 2012-04-16 2019-08-27 Vita Zahnfabrik H. Rauter Gmbh & Co. Kg Process for producing a non-dense sintered ceramic molded body having at least two layers

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4604366A (en) * 1984-03-20 1986-08-05 Dentsply Research & Development Corp. Leucite porcelain
EP0364281A3 (en) * 1988-10-14 1991-01-09 Warden-Pitts Dental Labs, Inc. Spray opaque composition for coating dental appliances
DE3911460A1 (en) * 1989-04-05 1990-10-11 Ducera Dental Gmbh Low-melting dental ceramic of high thermal expansion and corrosion resistance
DE4031168A1 (en) * 1990-10-03 1992-04-16 Degussa CERAMIC MATERIAL FOR VENEERING METALLIC DENTAL REPLACEMENT
FR2702649B1 (en) * 1993-03-16 1995-06-09 Sofraced Sa PROCESS AND KIT FOR MAKING A CERAMIC CUP TO PREPARE A DENTAL RECONSTRUCTION.
JP3879876B2 (en) * 1997-06-16 2007-02-14 株式会社トクヤマ Ceramic dental crown ceramic composition
ATE488475T1 (en) * 2002-07-22 2010-12-15 Enamelite Llc AEROSOLATED CERAMIC PORCELAIN AND GLAZING COMPOSITIONS
US7279238B2 (en) 2002-12-23 2007-10-09 Pentron Ceramics, Inc. Pressable glass-ceramics with textured microstructure

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS512664B2 (en) * 1971-08-25 1976-01-28
US4159358A (en) * 1977-05-19 1979-06-26 Board Of Regents, State Of Florida Method of bonding a bioglass to metal
JPS553301A (en) * 1977-08-03 1980-01-11 Wada Seimitsu Shiken Method of manufacturing dental porcelain baked cast crown

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0631995A1 (en) 1993-06-24 1995-01-04 Dentsply GmbH Dental prosthesis
US5849068A (en) * 1993-06-24 1998-12-15 Dentsply G.M.B.H. Dental prosthesis
US6126732A (en) * 1993-06-24 2000-10-03 Dentsply Detrey Gmbh Dental prosthesis
WO2011098115A1 (en) * 2010-02-09 2011-08-18 Vita Zahnfabrik H. Rauter Gmbh & Co. Kg A process for improving the stability of yttrium stabilised zirconia for dental restorations
US10391671B2 (en) 2012-04-16 2019-08-27 Vita Zahnfabrik H. Rauter Gmbh & Co. Kg Process for producing a non-dense sintered ceramic molded body having at least two layers
US11034051B2 (en) 2012-04-16 2021-06-15 Vita Zahnfabrik H. Rauter Gmbh & Co. Kg Non-dense sintered ceramic molded body having at least two layers

Also Published As

Publication number Publication date
DK69385D0 (en) 1985-02-14
EP0152338A2 (en) 1985-08-21
EP0152338A3 (en) 1985-09-18
JPS60195033A (en) 1985-10-03
FR2559386A1 (en) 1985-08-16
DE3571390D1 (en) 1989-08-17
ES540354A0 (en) 1985-12-01
FR2559386B1 (en) 1987-10-23
EP0152338B1 (en) 1989-07-12
DK69385A (en) 1985-08-16
ATE44455T1 (en) 1989-07-15
ES8601678A1 (en) 1985-12-01

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