Delamination resistant glass containers with heat-tolerant coatings
US-10273049-B2 · Apr 30, 2019 · US
US10787292B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10787292-B2 |
| Application number | US-201715656721-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 21, 2017 |
| Priority date | Jun 28, 2012 |
| Publication date | Sep 29, 2020 |
| Grant date | Sep 29, 2020 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Disclosed herein are delamination resistant glass pharmaceutical containers which may include an aluminosilicate glass having a Class HGA 1 hydrolytic resistance when tested according to ISO 720-1985 testing standard. The glass containers may also have a compressive stress layer with a depth of layer of greater than 25 μm. A surface compressive stress of the glass containers may be greater than or equal to 350 MPa. The delamination resistant glass pharmaceutical containers may be ion exchange strengthened and the ion exchange strengthening may include treating the delamination resistant glass pharmaceutical container in a molten salt bath for a time less than or equal to 5 hours at a temperature less than or equal to 450° C.
Opening claim text (preview).
What is claimed is: 1. A glass pharmaceutical container comprising: an aluminosilicate glass having a Class HGA 1 hydrolytic resistance when tested according to ISO 720-1985 testing standard, the aluminosilicate glass comprising greater than 70 mol. % and less than or equal to 80 mol. % of SiO 2 , the aluminosilicate glass comprising X mol. % of Al 2 O 3 and Y mol. % of alkali oxides and a ratio Y:X is greater than or equal to about 1 and less than or equal to about 2, the aluminosilicate glass comprising CaO and MgO in amounts such that a molar ratio of CaO/(CaO+MgO) is less than 0.5, and wherein a molar ratio of B 2 O 3 /(Y−X) in the aluminosilicate glass composition is from 0 to 0.3; a compressive stress layer with a depth of layer of greater than 25 μm; and a surface compressive stress of greater than or equal to 350 MPa, wherein the glass pharmaceutical container is ion exchange strengthened and the ion exchange strengthening comprises treating the glass pharmaceutical container in a molten salt bath for a time less than or equal to 5 hours at a temperature less than or equal to 450° C. 2. The glass pharmaceutical container of claim 1 , wherein the glass pharmaceutical container has a Type HGA1 hydrolytic resistance according to ISO 720:1985 after ion exchange strengthening. 3. The glass pharmaceutical container of claim 1 , wherein the glass pharmaceutical container has a threshold diffusivity of greater than 16 μm 2 /hr at a temperature of less than or equal to 450° C. 4. The glass pharmaceutical container of claim 1 , wherein the glass pharmaceutical container has a threshold diffusivity of greater than or equal to 20 μm 2 /hr at a temperature of less than or equal to 450° C. 5. The glass pharmaceutical container of claim 1 , wherein the glass pharmaceutical container is free of boron and compounds of boron. 6. The glass pharmaceutical container of claim 1 , wherein a concentration of B 2 O 3 in the glass pharmaceutical container is greater than or equal to about 0.01 mol. %. 7. The glass pharmaceutical container of claim 6 , wherein the concentration of B 2 O 3 in the glass pharmaceutical container is less than about 4 mol. %. 8. A glass pharmaceutical container comprising at least one of: a Type HGB1 hydrolytic resistance according to ISO 719:1985; at least a Class A2 base resistance or better according to ISO 695:1991; or at least a Class S2 acid resistance according to DIN 12116:2001; and the glass pharmaceutical container has a compressive stress layer with a depth of layer of greater than 25 μm; a glass composition comprising greater than 70 mol. % and less than or equal to 80 mol. % SiO 2 , the glass composition comprising X mol. % of Al 2 O 3 and Y mol. % of alkali oxides and a ratio Y:X is greater than or equal to about 1 and less than or equal to about 2, the glass composition comprising CaO and MgO in amounts such that a molar ratio of CaO/(CaO+MgO) is less than 0.5, and a molar ratio of B 2 O 3 /(Y−X) in the glass composition is from 0 to 0.3; and a surface compressive stress of greater than or equal to 200 MPa, wherein the glass pharmaceutical container is ion exchange strengthened and the ion exchange strengthening comprises treating the glass pharmaceutical container in a molten salt bath for a time less than or equal to 10 hours at a temperature less than or equal to 450° C. 9. The glass pharmaceutical container of claim 8 , wherein the glass pharmaceutical container is free from boron and compounds of boron. 10. The glass pharmaceutical container of claim 8 , wherein a concentration of B 2 O 3 in the glass pharmaceutical container is greater than or equal to about 0.01 mol. %. 11. The glass pharmaceutical container of claim 10 , wherein the concentration of B 2 O 3 in the glass pharmaceutical container is less than about 4 mol. %. 12. The glass pharmaceutical container of claim 8 , wherein the surface compressive stress is greater than or equal to 250 MPa. 13. A glass pharmaceutical container comprising at least one of: a Type HGB1 hydrolytic resistance according to ISO 719:1985; or a Type HGA1 hydrolytic resistance according to ISO 720:1985; wherein the pharmaceutical container is ion exchange strengthened and comprises a compressive stress layer with a depth of layer of greater than 15 μm and a surface compressive stress of greater than or equal to 350 MPa; wherein the ion exchange strengthening comprises treating the pharmaceutical container in a molten salt bath for a time less than or equal to 10 hours at a temperature less than or equal to 500° C.; and wherein the glass pharmaceutical container comprises a glass composition which is free from boron and compounds of boron such that the glass pharmaceutical container does not delaminate, the glass composition comprising X mol. % of Al 2 O 3 and Y mol. % of alkali oxides and a ratio Y:X is greater than or equal to about 1 and less than or equal to about 2, the glass composition comprising CaO and MgO in amounts such that a molar ratio of CaO/(CaO+MgO) is less than 0.5. 14. The glass pharmaceutical container of claim 13 , wherein the glass pharmaceutical container has a threshold diffusivity of greater than 16 μm 2 /hr at a temperature of less than or equal to 450° C. 15. The glass pharmaceutical container of claim 13 , wherein the glass pharmaceutical container has a threshold diffusivity of greater than or equal to 20 μm 2 /hr at a temperature of less than or equal to 450° C.
to perform ion-exchange between alkali ions (C03C21/005 takes precedence) · CPC title
at least one coating of an organic material and at least one non-metal coating · CPC title
with at least two coatings of organic materials (C03C17/36, C03C17/42 take precedence) · CPC title
with synthetic or natural resins (C03C17/30 takes precedence) · CPC title
with silicon-containing compounds · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.