Method for suppressing crystallization of fluoride glass articles by treatment with inorganic fluoride

• US 5,147,435 A
• Filed: 05/13/1991
• Issued: 09/15/1992
• Est. Priority Date: 05/23/1990
• Status: Expired due to Fees

• Current Assignee: Central Glass Company Limited
• Original Assignee: Central Glass Company Limited
• Inventors: Kita, Yasushi, Kubota, Yoshinori, Sakanoue, Akira
• Primary Examiner(s): LINDSAY JR, ROBERT
• Application Number:
  US07/698,896
• Time in Patent Office: 491 Days
• Field of Search: 65/3.11, 65/30.1, 65/33, 65/DIG. 16
• US Class Current: 65/30.1
• CPC Class Codes: C03C 17/22 with other inorganic material C03C17/34, C03C17/44 take precedence
• CPC Class Codes: C03C 2217/285 Fluorides
• CPC Class Codes: C03C 2218/11 from solutions or suspensions
• CPC Class Codes: Y10S 65/16 Optical filament or fiber treatment with fluorine or incorporating fluorine in final product

Abstract

Crystallization of a fluoride glass article is suppressed by treating the surface(s) of the fluoride glass article with a solution of a fluorine-containing alkali metal compound or a fluorine-containing ammonium compound such as, e.g., LiPF₆, NaBF₄ or NH₄ BF₄, in a nonaqueous solvent such as, e.g., ethanol, N,N-dimethylformamide or acetonitrile. The treatment can be made at room temperature.

Claims

1. A method for suppressing crystallization of an article made of a glass consisting of metal fluorides, the method comprising the step of treating at least one surface of the glass article with a solution of an inorganic fluorine compound, which is selected from the group consisting of alkali metal compounds containing fluorine and ammonium compounds containing fluorine, in an organic solvent having no water by immersing the glass article in said solution for at least about 3 hr.

2. A method according to claim 1, wherein said fluorine compound is selected from the group consisting of LiPF₆, NaPF₆, KPF₆, LiBF₄, NaBF₄, KBF₄, K₂ SiF₆, K₂ TiF₆, Na₂ SiF₆, NH₄ F, NH₄ F.HF and NH₄ BF₄.

3. A method according to claim 1, wherein said organic solvent is selected from the group consisting of methanol, ethanl, 1-propanol, 2-chloroethanol, 2-aminoethanol and ethylene glycol.

4. A method according to claim 1, wherein said organic solvent is selected from the group consisting of formamide, N-methylformamide, N,N-dimethylformamide, N-methylpropionamide, acetonitrile and acrylonitrile.

5. A method according to claim 1, wherein said organic solvent is selected from the group consisting of dimethyl ether, diethyl ether, ethylene carbonate, propylene carbonate, dimethoxyethane, ethyl acetate and dimethyl sulfoxide.

6. A method according to claim 1, wherein said organic solvent is ethanol, said fluorine compound being selected from the group consisting of LiPF₆, KPF₆, KBF₄, K₂ SiF₆, K₂ TiF₆, NaBF₄, Na₂ SiF₆, NH₄ F, NH₄ F.HF and NH₄ BF₄.

7. A method according to claim 1, wherein said organic solvent is N,N-dimethylformamide, said fluorine compound being selected from the group consisting of LiPF₆, NaPF₆, K₂ SiF₆, K₂ TiF₆, LiBF₄, NaBF₄, Na₂ SiF₆, NH₄ F, NH₄ F.HF and NH₄ BF₄.

8. A method according to claim 1, wherein said organic solvent is acetonitrile, said fluorine compound being selected from the group consisting of LiPF₆, K₂ TiF₆, NaBF₄, NH₄ F, NH₄ F.HF and NH₄ BF₄.

9. A method according to claim 1, wherein the treatment is made at room temperature.

10. A method according to claim 1, wherein said solution is prepared by dissolving up to 1 mol of said inorganic fluorine compound in 1 kg of said organic solvent.

11. A method according to claim 10, wherein the solubility of said inorganic fluorine compound in said organic solvent is less than 1 mol/kg solvent at room temperature, said solution being a saturated solution.