WO2002100792A1 - Method for reducing the amount of lithium in glass production - Google Patents
Method for reducing the amount of lithium in glass production Download PDFInfo
- Publication number
- WO2002100792A1 WO2002100792A1 PCT/US2002/018316 US0218316W WO02100792A1 WO 2002100792 A1 WO2002100792 A1 WO 2002100792A1 US 0218316 W US0218316 W US 0218316W WO 02100792 A1 WO02100792 A1 WO 02100792A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- batch
- glass
- glass batch
- lithium
- amount
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C1/00—Ingredients generally applicable to manufacture of glasses, glazes, or vitreous enamels
Definitions
- the present invention relates to glass batch forming methods.
- it relates to a method wherein a calcium magnesium silicate is substituted for lithium as a melting aid in glass batches.
- Glass batches can contain certain materials as melting aids. These aids assist in creating a homogeneous batch having complete reactions and performed at lower melting temperatures or times.
- One such melting aid is lithium, which while effective is relatively expensive to use. There remains a need to further develop useful melting aids which can be used in conjunction with or in the absence of lithium compounds.
- One object of the present invention is a method of producing a glass batch composition having favorable viscosity characteristics. Another objective is to provide a melting aid for a glass batch which can work in conjunction with or as a partial or total replacement for lithium melting aids. These and other objectives are achieved by a DN 01-017
- One embodiment of the present invention is a method of producing a glass batch composition composed of a calcium magnesium silicate and other glass components to produce a glass batch.
- the glass batch composition is then melted to form a melted glass batch composition.
- the amount of said calcium magnesium silicate used is selected effectively to produce a viscosity character and batch free time in the glass batch composition less than or equal to that which results from use of an equivalent amount of a lithium compound in a comparative glass batch.
- An equivalent amount is the use of the same mass percent of the calcium magnesium silicate or lithium compound in the total glass batch before heating.
- the calcium magnesium silicate of the present invention can be a natural resource or one attained by synthetic produced.
- a preferred calcium magnesium silicate compound is that described in U, S, Patent No.6,211,103 Bl.
- a more preferred calcium magnesium silicate has an empirical formula of Ca x Mg y SiO x , and the values of x and y are independently from about 0.1 to about 0.6 and z is a value to balance the oxidation state of the compound. DN 01-017
- the respective amounts of the calcium magnesium silicate compound and other glass components is dependent upon the glass formula being produced.
- the term "comparative glass batch” or “comparative glass product” means a glass batch or product which is equivalent in oxide values, except that the value of boron oxide equivalent is less for an embodied glass product made with the present invention than that made with known processes which do not use a calcium magnesium silicate compound as described herein. It has been unexpectedly discovered that by using the calcium magnesium silicate compound described herein that less lithium values are needed to attain the same or better result as the amount used in known methods. Accordingly, a preferred method is one in which the other batch components comprise less than about one percent by total batch weight of lithium. It was further unexpectedly found that in the method using calcium oxide silicate compounds to reduce the amount of lithium needed for a particular purpose, that the use of an embodied calcium magnesium silicate compound enabled as a preferred method to reduce the amount of said magnesium oxide compound to about zero.
- the amount of the calcium magnesium silicate compound used can be adjusted so that the viscosity of the formed glass batch is at least about ten percent less than that of the comparative glass batch. Similarly, the amount of the calcium magnesium silicate compound used can be adjusted so that the batch free time of the formed glass batch is at least about ten percent less than that of the comparative glass batch.
- an amount of a feldsparthic compound can be combined with the calcium magnesium silicate compound t achieve similar results.
- the above method is modified by the additional mixing of a feldspathic component.
- a feldspathic component can be one of any of the numerous natural or synthetic forms of feldspar or feldspar-type material.
- Such feldspathic material is an aluminosilicate with barium, calcium, potassium, or sodium component preferably is a potassium aluminosilicate having the formula KAlSi 3 O 8 with little sodium values.
- An inventive sample is made by adding together feldspar, calcium magnesium
- the calcium magnesium silicate is Synsil®
- silicate from Synsil Products Inc., and has the following composition:
- the feldspar is a potassium aluminosilicate.
- the glass produced from the glass batch is a potassium aluminosilicate.
- a comparative batch is produced using 7 mass percent dolomite, 5 mass percent spodumene, and the balance being the other glass forming components.
- a comparison of the glasses produced show that the experimental glass is produced with reduced batch free time while retaining similar glass properties as the comparative glass.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Glass Compositions (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP02734757A EP1397317A1 (en) | 2001-06-11 | 2002-06-10 | Method for reducing the amount of lithium in glass production |
JP2003503564A JP2004529061A (en) | 2001-06-11 | 2002-06-10 | Method for reducing lithium content in glass production |
CA002446421A CA2446421A1 (en) | 2001-06-11 | 2002-06-10 | Method for reducing the amount of lithium in glass production |
BR0209928-4A BR0209928A (en) | 2001-06-11 | 2002-06-10 | Method of Producing a Glass Batch Composition |
MXPA03011470A MXPA03011470A (en) | 2001-06-11 | 2002-06-10 | Method for reducing the amount of lithium in glass production. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/878,643 | 2001-06-11 | ||
US09/878,643 US6531421B2 (en) | 2001-06-11 | 2001-06-11 | Method of reducing the amount of lithium in glass production |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2002100792A1 true WO2002100792A1 (en) | 2002-12-19 |
Family
ID=25372491
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2002/018316 WO2002100792A1 (en) | 2001-06-11 | 2002-06-10 | Method for reducing the amount of lithium in glass production |
Country Status (10)
Country | Link |
---|---|
US (1) | US6531421B2 (en) |
EP (1) | EP1397317A1 (en) |
JP (1) | JP2004529061A (en) |
CN (1) | CN1250473C (en) |
BR (1) | BR0209928A (en) |
CA (1) | CA2446421A1 (en) |
CZ (1) | CZ20033386A3 (en) |
MX (1) | MXPA03011470A (en) |
PL (1) | PL369633A1 (en) |
WO (1) | WO2002100792A1 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7383699B2 (en) * | 2001-12-27 | 2008-06-10 | Specialty Minerals (Michigan) Inc. | Method of manufacturing glass and compositions therefore |
US7937969B2 (en) * | 2004-08-26 | 2011-05-10 | Carty William M | Selective batching for boron-containing glasses |
BRPI0712438A2 (en) * | 2006-06-01 | 2012-05-29 | Agc Flat Glass Europe Sa | lime glass group composition |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3941574A (en) * | 1973-05-21 | 1976-03-02 | Garegin Sarkisovich Melkonian | Method of preparing a glass batch for melting silicate glass |
EP0320232A2 (en) * | 1987-12-10 | 1989-06-14 | Pilkington Plc | Producing molten glass and batch components therefor |
WO1999033765A1 (en) * | 1997-12-31 | 1999-07-08 | Minerals Technologies Inc. | Method of producing synthetic silicates and use thereof in glass production |
US6211103B1 (en) * | 1999-10-12 | 2001-04-03 | Minerals Technologies Inc. | Synthetic silicate pellet compositions |
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US3001884A (en) * | 1958-11-12 | 1961-09-26 | Kunstzijdespinnerij Nyma Nv | Mixtures of cellulose ethers and starch ethers |
DK105386C (en) | 1964-02-28 | 1966-09-19 | Kroyer K K K | Process for the production of ceramic materials. |
GB1173777A (en) | 1965-12-27 | 1969-12-10 | Saint Gobain | Pretreated Batch Material for making Glass and other Silicates, and a Process and Apparatus for its Manufacture |
US3520705A (en) | 1966-05-10 | 1970-07-14 | Onoda Cement Co Ltd | Non-vitreous ceramic ware made from pseudowollastonite |
US3381064A (en) | 1966-11-30 | 1968-04-30 | Onoda Cement Co Ltd | Method of making pseudowollastonite clinker with the rotary kiln |
FR1559817A (en) | 1968-01-23 | 1969-03-14 | ||
US3926647A (en) | 1970-12-30 | 1975-12-16 | Rheinische Kalksteinwerke | Process for the production of synthetic wollastonite and diopside |
US3802901A (en) | 1972-09-05 | 1974-04-09 | Fmc Corp | Method of forming granular alkaline earth carbonates |
CH583147A5 (en) | 1973-05-30 | 1976-12-31 | Pelltec Sa | |
US3875288A (en) | 1973-08-17 | 1975-04-01 | Nl Industries Inc | Production of synthetic silicate minerals |
US4110097A (en) | 1974-08-14 | 1978-08-29 | Saint-Gobain Industries | Method for the manufacture of glass |
US3967943A (en) | 1974-10-30 | 1976-07-06 | Anchor Hocking Corporation | Method of improving glass batch melting by use of water glass |
US3969100A (en) | 1975-02-27 | 1976-07-13 | Ford Motor Company | Method of pelletizing glass batch materials |
US4026691A (en) | 1975-11-03 | 1977-05-31 | The Dow Chemical Company | Making a pelletized glass batch for soda-lime glass manufacture |
US4023976A (en) | 1976-01-23 | 1977-05-17 | Fmc Corporation | Manufacture of glass using briquettes |
JPS53139621A (en) | 1977-05-13 | 1978-12-06 | Ishikawa Takashi | Inorganic light weight aggregate |
JPS54123118A (en) | 1978-03-16 | 1979-09-25 | Nippon Sheet Glass Co Ltd | Granulation of glass raw material |
EP0015794B1 (en) | 1979-02-22 | 1984-05-30 | Rhone-Poulenc Chimie De Base | Process for obtaining a glass composition based on metallic silicates and having a low melting point and improved refining properties |
JPS55149122A (en) | 1979-05-09 | 1980-11-20 | Tokuyama Soda Co Ltd | Manufacture of calcium sodium silicate hydrate |
JPS5964563A (en) | 1982-10-04 | 1984-04-12 | 神奈川県 | Manufacture of lightweight formed body |
US4474594A (en) | 1983-02-14 | 1984-10-02 | Pq Corporation | Method for forming compacted bodies of glassmaking raw materials |
US4519814A (en) | 1983-07-25 | 1985-05-28 | Ppg Industries, Inc. | Two stage batch liquefaction process and apparatus |
US4634461A (en) | 1985-06-25 | 1987-01-06 | Ppg Industries, Inc. | Method of melting raw materials for glass or the like with staged combustion and preheating |
US4920080A (en) | 1988-08-19 | 1990-04-24 | Ppg Industries, Inc. | Method of making glass with preliminary reaction of batch materials |
JP2763929B2 (en) | 1988-08-31 | 1998-06-11 | 秩父小野田株式会社 | Method for producing high-strength calcium silicate compact |
JPH03228831A (en) | 1990-01-31 | 1991-10-09 | Nippon Sheet Glass Co Ltd | Method for granulating briquet batch |
DE4228500A1 (en) | 1992-09-01 | 1994-03-03 | Michaela Mueller | Mineral, hardenable foam structure - produced by reacting metal oxide(s) with aq. solns. of alkali silicates, with addn. of inert fillers, etc. |
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JPH09285849A (en) | 1996-04-23 | 1997-11-04 | Mitsubishi Heavy Ind Ltd | Belt coating agent for belt type continuous casting |
US6287997B1 (en) * | 1996-09-03 | 2001-09-11 | Minerals Technologies Inc. | Method of producing synthetic silicates and use thereof in glass production |
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-
2001
- 2001-06-11 US US09/878,643 patent/US6531421B2/en not_active Expired - Fee Related
-
2002
- 2002-06-10 PL PL02369633A patent/PL369633A1/en not_active Application Discontinuation
- 2002-06-10 WO PCT/US2002/018316 patent/WO2002100792A1/en not_active Application Discontinuation
- 2002-06-10 BR BR0209928-4A patent/BR0209928A/en not_active Application Discontinuation
- 2002-06-10 CZ CZ20033386A patent/CZ20033386A3/en unknown
- 2002-06-10 CA CA002446421A patent/CA2446421A1/en not_active Abandoned
- 2002-06-10 JP JP2003503564A patent/JP2004529061A/en not_active Withdrawn
- 2002-06-10 MX MXPA03011470A patent/MXPA03011470A/en unknown
- 2002-06-10 CN CNB028103793A patent/CN1250473C/en not_active Expired - Fee Related
- 2002-06-10 EP EP02734757A patent/EP1397317A1/en not_active Ceased
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3941574A (en) * | 1973-05-21 | 1976-03-02 | Garegin Sarkisovich Melkonian | Method of preparing a glass batch for melting silicate glass |
EP0320232A2 (en) * | 1987-12-10 | 1989-06-14 | Pilkington Plc | Producing molten glass and batch components therefor |
WO1999033765A1 (en) * | 1997-12-31 | 1999-07-08 | Minerals Technologies Inc. | Method of producing synthetic silicates and use thereof in glass production |
US6211103B1 (en) * | 1999-10-12 | 2001-04-03 | Minerals Technologies Inc. | Synthetic silicate pellet compositions |
Also Published As
Publication number | Publication date |
---|---|
MXPA03011470A (en) | 2005-03-07 |
CN1511117A (en) | 2004-07-07 |
BR0209928A (en) | 2004-03-30 |
CA2446421A1 (en) | 2002-12-19 |
EP1397317A1 (en) | 2004-03-17 |
CN1250473C (en) | 2006-04-12 |
US6531421B2 (en) | 2003-03-11 |
PL369633A1 (en) | 2005-05-02 |
JP2004529061A (en) | 2004-09-24 |
CZ20033386A3 (en) | 2004-09-15 |
US20020198092A1 (en) | 2002-12-26 |
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