Method For The Preparation Of Glasses And Glass Ceramics With SiO2 As Main Crystal Phase

Patent metadata

Field	Value
Publication number	US-2019352220-A1
Application number	US-201916527727-A
Country	US
Kind code	A1
Filing date	Jul 31, 2019
Priority date	Nov 11, 2015
Publication date	Nov 21, 2019
Grant date	—

Abstract

The invention also relates to a glass ceramic and a glass which can be obtained using the method according to the invention, the use thereof as dental material and in particular for the preparation of dental restorations, as well as a glass-forming composition which is suitable for use in the method according to the invention.

First claim

1 . Method for the preparation of a dental restoration, which process comprises
(a) preparing a glass ceramic with SiO 2 as main crystal phase or a glass which comprises nuclei for the crystallization of SiO 2 in a process which comprises a step in which a melt of a starting glass which comprises cerium ions is exposed to reducing conditions, and (b) shaping the glass ceramic or the glass with nuclei by pressing or machining to form the desired dental restoration.

2 . Method according to claim 1 , wherein the dental restoration is an inlay, onlay, veneer, partial crown, crown or facet.

3 . Method according to claim 1 , wherein the melt of the starting glass is reacted with at least one reducing agent.

4 . Method according to claim 3 , wherein the at least one reducing agent is a reducing gas.

5 . Method according to claim 4 , wherein the reducing gas comprises hydrogen or hydrogen and nitrogen.

6 . Method according to claim 1 , wherein the melt of the starting glass is formed from a glass-forming composition which comprises SiO 2 , Li 2 O, a cerium compound and at least one reducing agent.

7 . Method according to claim 3 , wherein the at least one reducing agent is a compound which comprises at least one oxidizable carbon atom.

8 . Method according to claim 7 , wherein the at least one reducing agent is an acetylacetonate.

9 . Method according to claim 1 , wherein the starting glass comprises 0.1 to 7.0 wt.-% cerium ions, calculated as CeO 2 .

10 . Method according to claim 1 , wherein the starting glass further comprises terbium ions.

11 . Method according to claim 10 , wherein the starting glass comprises 0.05 to 2.0 wt.-% terbium ions, calculated as Tb 4 O 7 .

12 . Method according to claim 1 , in which the starting glass comprises 0 to 11.0 wt.-% alkaline earth metal oxide.

13 . Method according to claim 1 , in which the starting glass comprises at least one of the following components in the given quantities:

Component
wt.-%

SiO 2
58.0 to 92.0  

Li 2 O
2.0 to 10.0 

CeO 2
0.1 to 7.0  

Tb 4 O 7
0 to 2.0

Me I 2 O
 0 to 13.0

Me II O
 0 to 11.0

Me III 2 O 3
 0 to 10.0

Me IV O 2
 0 to 21.0

P 2 O 5
0 to 7.0

Me V 2 O 5
0 to 6.0

Me VI O 3
0 to 6.0

fluorine
 0 to 5.0,

wherein
Me I 2 O is selected from Na 2 O, K 2 O, Rb 2 O and/or Cs 2 O,
Me II O is selected from MgO, CaO, SrO and/or ZnO,
Me III 2 O 3 is selected from Al 2 O 3 , B 2 O 3 , Y 2 O 3 , La 2 O 3 , Ga 2 O 3 and/or In 2 O 3 ,
Me IV O 2 is selected from ZrO 2 , GeO 2 , TiO 2 and/or SnO 2 ,
Me V 2 O 5 is selected from V 2 O 5 , Ta 2 O 5 and/or Nb 2 O 5 and
Me VI O 3 is selected from WO 3 and/or MoO 3 .

14 . Method according to claim 1 , wherein the glass with nuclei comprises nuclei which are suitable for forming low quartz, cristobalite or a mixture thereof.

15 . Method according to claim 1 , wherein the glass ceramic has low quartz, cristobalite or a mixture thereof as main crystal phase.

16 . Method according to claim 1 , wherein the glass ceramic comprises 5.0 to 50.0 wt.-% SiO 2 as crystal phase.

17 . Method according to claim 1 , wherein the glass ceramic comprises 10.0 to 30.0 wt.-% SiO 2 as crystal phase.

18 . Method according to claim 1 , wherein the starting glass is subjected to at least one heat treatment in the range of from 700 to 950° C.

19 . Method according to claim 1 , wherein the glass ceramic or the glass are present in the form of a powder, a blank or a dental restoration.

20 . Method according to claim 1 , wherein the glass ceramic or the glass have a fluorescence intensity at 420 nm or at 541 nm which is at least 1.5 times the corresponding fluorescence intensity of a reference sample,
wherein the reference sample is obtainable by melting a starting glass with the composition: 74.3 wt.-% SiO 2 , 7.7 wt.-% Li 2 O, 3.4 wt.-% K 2 O, 1.8 wt.-% MgO, 3.3 wt.-% CaO, 4.0 wt.-% Al 2 O 3 , 3.6 wt.-% P 2 O 5 , 1.5 wt.-% CeO 2 and 0.4 wt.-% Tb 4 O 7 on a scale of 200 g from suitable raw materials in a platinum-rhodium crucible at 1650° C. for 1 h, pouring 30 g of the glass melt into a pre-heated mould in order to produce a glass block, and converting the glass block into a glass ceramic by successive temperature treatments at 530° C. for 20 min and 800° C. for 30 min, wherein the heating rates between the temperature treatments are 30 K/min in each case.

Assignees

• Ivoclar Vivadent Ag

Inventors

• Rampf Markus
• Krolikowski Sebastian
• Ritzberger Christian
• Höland Wolfram
• Schweiger Marcel

Classifications

• C03C10/0009 Primary

  containing silica as main constituent · CPC title

• C03C4/02

  for coloured glass · CPC title

• C03C4/12

  for luminescent glass; for fluorescent glass · CPC title

• C03C4/0021

  for dental use · CPC title

• A61C8/0048

  Connecting the upper structure to the implant, e.g. bridging bars (A61C8/0028 takes precedence) · CPC title