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
  • C03C21/00—Treatment of glass, not in the form of fibres or filaments, by diffusing ions or metals in the surface
  • C03C21/001—Treatment of glass, not in the form of fibres or filaments, by diffusing ions or metals in the surface in liquid phase, e.g. molten salts, solutions
  • C03C21/002—Treatment of glass, not in the form of fibres or filaments, by diffusing ions or metals in the surface in liquid phase, e.g. molten salts, solutions to perform ion-exchange between alkali ions
• • A—HUMAN NECESSITIES
  • A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
  • A47G—HOUSEHOLD OR TABLE EQUIPMENT
  • A47G19/00—Table service
  • A47G19/02—Plates, dishes or the like
• • A—HUMAN NECESSITIES
  • A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
  • A47G—HOUSEHOLD OR TABLE EQUIPMENT
  • A47G19/00—Table service
  • A47G19/22—Drinking vessels or saucers used for table service
  • A47G19/2205—Drinking glasses or vessels
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
  • C03B27/00—Tempering or quenching glass products
  • C03B27/012—Tempering or quenching glass products by heat treatment, e.g. for crystallisation; Heat treatment of glass products before tempering by cooling
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
  • C03B27/00—Tempering or quenching glass products
  • C03B27/02—Tempering or quenching glass products using liquid
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
  • C03B27/00—Tempering or quenching glass products
  • C03B27/02—Tempering or quenching glass products using liquid
  • C03B27/03—Tempering or quenching glass products using liquid the liquid being a molten metal or a molten salt
• • 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
  • C03C23/00—Other surface treatment of glass not in the form of fibres or filaments
  • C03C23/007—Other surface treatment of glass not in the form of fibres or filaments by thermal treatment
• • 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
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
  • C03C3/091—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
• • A—HUMAN NECESSITIES
  • A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
  • A47G—HOUSEHOLD OR TABLE EQUIPMENT
  • A47G2400/00—Details not otherwise provided for in A47G19/00-A47G23/16
  • A47G2400/10—Articles made from a particular material

Definitions

• the invention relates to a method for increasing the strength, in particular the transverse rupture strength, of a glass object made from a glass material, namely alkali-earth-alkaline silicate glass or borosilicate glass.
• the invention also relates to a glass article made by the method according to the invention.
• thermal tempering columnloquially also referred to as thermal hardening or tempering
• the glass workpiece to be strengthened is heated to approx. 600 °C in a furnace and then quickly quenched to room temperature. This quenching solidifies the surface and the external dimensions of the component change only slightly. Compressive stresses arise on the surface of the glass workpiece, which ultimately lead to greater breaking strength.
• Thermal toughening is used in particular in the manufacture of toughened safety glass (ESG).
• ESG toughened safety glass
• the stress profile of toughened safety glass shows high internal tensile stresses across the glass thickness, which lead to a characteristic crumbly fracture pattern if the pane fails.
• the treatment time in the molten salt is disadvantageously very long. It is usually between 8 and 36 hours.
• the problem of long process times can be reduced by using expensive special glasses with the simultaneous use of complicated, in particular multi-stage, treatment processes.
• DD 1579 66 discloses a method and a device for strengthening glass products by ion exchange.
• the glass products are strengthened by alkali ion exchange between the glass surface and alkali salt melts.
• hollow glass products with the opening facing downwards or hollow glass products that are rotated or pivoted about a horizontal axis are sprinkled with molten salt.
• the salt is constantly circulated and passed through perforated plates in order to create a rain cascade for the glass products arranged in several layers.
• this method can only be used in an economically viable manner when using comparatively expensive special glass.
• DE 195 10 202 C2 discloses a method for producing hollow glass bodies using the blow-blow and press-blow shaping method with increased mechanical strength.
• the method is characterized in that mist-like aqueous alkali metal salt solutions are added to the compressed air in the preliminary and/or finished mold of the blow-blow molding process or in the finished mold of the press-blow molding process.
• the glass is preheated to a temperature of 100 °Celsius and then immersed in melted salt.
• the task is solved by a method which is characterized by the following steps: a. heating the glass article to a first temperature above the glass transition temperature, b. shock cooling the glass article to a second temperature which is below the transformation temperature of the glass material, the shock cooling being effected by contacting the glass article with a cooling medium which has the second temperature, c. performing an ion exchange process at the second temperature for a time ranging from 15 minutes to 45 minutes.
• the method according to the invention is based on a skillful combination of thermal and chemical hardening and can be carried out in an advantageous and surprising manner in a comparatively simple, quick and uncomplicated manner. Nevertheless, the method of the present invention offers both significant advantages over thermal toughening and significant advantages over chemical toughening.
• the method according to the invention can be used to achieve very high strength values, in particular with regard to transverse rupture strength, microhardness and scratch resistance, which exceed the strength values of untreated glass many times over, but the required process times are very short compared to the process times that are usual Process of chemical toughening include. It has been shown that the ion exchange time in the method according to the invention generally needs to be less than 30 minutes in order to be able to achieve strength values that are similar to those achieved by conventional chemical strengthening methods with very long process times and that better ones Strength values are achieved than with pure thermal hardening. The method according to the invention is therefore particularly advantageous for industrial mass production of hardened glass objects.
• a further advantage of the method according to the invention is that it offers a very high level of flexibility with regard to the possible wall thicknesses and the possible shapes of the glass objects to be treated.
• the method according to the invention is suitable both for increasing the strength of flat glass, for example for windows or displays, and for increasing the strength of differently shaped glass objects, in particular vessels and/or crockery objects.
• the invention has the very special advantage that in particular comparatively inexpensive glass material, such as simple utility glass, in particular container glass, can be used as the starting material in order to obtain particularly break-resistant glass objects as a result.
• comparatively inexpensive glass material such as simple utility glass, in particular container glass
• the invention also has the very special advantage that a smaller wall thickness of the glass object is required, in particular for objects of daily use, due to the increased breaking strength.
• the consequence of this is that glass can be saved in the production of the glass objects compared to glass objects conventionally produced from the same glass material.
• the glass objects treated according to the invention can therefore have a lower intrinsic weight than glass objects conventionally produced from the same glass material.
• the first temperature is in a range from 100 Kelvin to 300 Kelvin above the transformation temperature.
• the first temperature lies in a range of 50 Kelvin below and 30 Kelvin above the Littleton point of the glass material.
• the transformation temperature is the temperature at which the glass changes from the plastic state to the rigid state during cooling; in particular the temperature at which the viscosity r
• the Littleton point is the temperature at which the viscosity r
• the glass object is heated in such a way that the initial heating rate is 100 Kelvin per minute, in particular over 250 Kelvin per minute.
• the glass object can advantageously be heated to a first temperature by transferring the glass object (in particular together with other glass objects of a batch) into an oven.
• the oven can advantageously have an oven temperature which corresponds to the Littleton point of the glass material or which is at most 50 Kelvin below and at most 30 Kelvin above the Littleton point of the glass material of the glass object.
• the oven can advantageously have an oven temperature which is in a range from 10 Kelvin to 40 Kelvin above the first temperature.
• the furnace temperature can advantageously be in the range from 650° Celsius to 770° Celsius, in particular in the range from 740° Celsius to 760° Celsius or in the range from 680° Celsius to 730° Celsius, lie or be 750 °Celsius.
• the glass article remains in the kiln long enough to reach (at least its outermost layer) the first temperature.
• the glass object must not remain in the oven for too long in order to avoid unwanted deformation of the glass object. It has been shown that particularly good results are achieved with glass objects that are designed as hollow bodies with a wall that has a wall thickness if the glass object is heated up for a time in the range from 35 seconds to 90 seconds, in particular from 45 seconds to 70 Seconds per millimeter of wall thickness, in particular for a heating time of 55 seconds per millimeter of wall thickness, remains in the furnace.
• the wall thickness at the thinnest point is preferably decisive for the heating-up time.
• the glass object is heated for a heating time in the range from 35 seconds to 90 seconds, in particular from 45 seconds to 70 seconds, per millimeter of thickness, in particular for a heating time of 55 seconds per millimeter of thickness, left in the oven.
• the thickness at the thinnest point is preferably decisive for the heating-up time.
• heating can be carried out in a particularly advantageous manner take place in a multi-stage, in particular two-stage, process.
• the glass object is first heated slowly to an intermediate temperature and then quickly heated to the first temperature.
• the glass object is first heated to an intermediate temperature at a first heating rate and is then heated to the first temperature at a second heating rate, which is higher than the first heating rate.
• This procedure has the particular advantage that unwanted deformations of the glass object are effectively avoided, since all areas of the glass object reach the first temperature at the same time or at least within a predetermined or specifiable time window. In this way, it is avoided that the areas of the glass object that can be heated up more quickly are already deformed (unintentionally) while it is still necessary to wait until other areas that can be heated up less quickly reach the first temperature.
• this procedure has the particular advantage that interactions between the glass object and the holder, which occur in particular at high temperatures and which hold and/or transport the glass object during the execution of the method, are avoided or at least reduced.
• the intermediate temperature is preferably in a range from 50 degrees Kelvin below to 100 Kelvin above the transformation temperature of the glass material, in particular in a range from 0 Kelvin to 50 Kelvin above the transformation temperature of the glass material.
• the oven temperature can be increased after the first heating-up phase, for example.
• a furnace is used which has furnace areas at different temperatures, so that after the first heating-up phase in a first furnace area, the glass object can be transferred to a second furnace area for the second heating-up phase.
• the glass object is first heated at a first oven temperature and then at a second oven temperature, which is higher than the first oven temperature. It is of particular advantage here if the glass object is exposed to the second oven temperature for a heating time in the range from 30 seconds to 120 seconds, in particular from 80 seconds to 100 seconds, or for a heating time of 90 seconds. In this way it is achieved that the glass object reaches the primary temperature everywhere without the glass object becoming deformed.
• the upper furnace temperature can advantageously be in the range from 680° Celsius to 730° Celsius.
• the chilling is carried out without delay once the glass article has reached the first temperature.
• the chilling is preferably carried out with a delay of no more than one minute after the glass article has reached the first temperature. In this way it is avoided that the glass object heated to the first temperature initially cools down again slowly, in particular to a temperature outside a range of 100 Kelvin to 300 Kelvin above the transformation temperature, before the shock cooling takes place. Particularly good strength values are achieved when the second temperature is in a range from 50 Kelvin to 200 Kelvin below the transformation temperature.
• the chilling is carried out by bringing the glass object into contact with a cooling agent which is a liquid or a suspension.
• the cooling medium has the second temperature.
• the shock cooling can be carried out by immersing the glass object in a cooling bath that contains the cooling agent.
• the contacting it is also possible, for example, for the contacting to take place by spraying or by sprinkling with the cooling agent, which preferably has the second temperature.
• the initial cooling rate is essentially determined by the difference between the primary temperature and the temperature of the coolant and by the material-specific heat transfer coefficient.
• particularly good results in terms of breaking strength are achieved when the first temperature and the cooling medium temperature are selected such that the initial cooling rate is in the range from 80 Kelvin to 120 Kelvin per second, in particular in the range from 90 Kelvin to 110 Kelvin per second , or 100 Kelvin per second.
• the ion exchange process preferably includes ions, in particular alkali ions, in particular sodium ions, to be removed from the glass object and to be replaced by spatially larger ions, in particular alkali ions, in particular potassium ions.
• the ion exchange process involves contacting the glass article with an exchange agent.
• a replacement agent is used in the form of a replacement salt melt or in the form of a paste or suspension containing a replacement salt.
• the exchange salt is potassium nitrate or contains potassium nitrate.
• the glass object can be brought into contact with the exchange agent by immersion or by spraying or by sprinkling.
• the cooling medium is also the exchange medium at the same time.
• the ion exchange process is carried out for a period ranging from 15 minutes to 45 minutes.
• very high strength values are achieved if the ion exchange process lasts for a period in the range from 20 minutes to 40 minutes, in particular for about 30 minutes.
• the glass material is preferably not an aluminosilicate glass because such glass is too complex and, in particular, too expensive to produce.
• the glass material preferably has an aluminum oxide content of less than 5% (percent by mass) (Al2O3 ⁇ 5%), in particular less than 4.5% (percent by mass) (Al2O3 ⁇ 4.5%).
• alkali-earth-alkaline silicate glass has the particular advantage that it can be obtained inexpensively, but can still be processed into particularly break-resistant glass objects using the method according to the invention.
• the first temperature can advantageously be in the range from 700° Celsius to 760° Celsius, in particular in the range from 720° Celsius to 740° Celsius.
• the temperature of the coolant especially if the coolant is, for example, a molten salt, such as molten sodium salt or molten potassium salt, can advantageously be in the range from 350° Celsius to 500° Celsius, in particular in the range from 390° Celsius to 450° Celsius or in the range from 420 °Celsius to 440 °Celsius, in particular in order to achieve the advantageous cooling rate mentioned above.
• a molten salt such as molten sodium salt or molten potassium salt
• the glass material can advantageously have a silicon dioxide content (SiO?) of more than 58% (percent by mass) and less than 85% (percent by mass), in particular more than 70% (percent by mass) and less than 74% (percent by mass).
• a glass material that is an alkali-earth-alkaline silicate glass can advantageously have a silicon dioxide content of more than 70% (percent by mass) and less than 74% (percent by mass).
• the glass material has an alkali oxide content, in particular sodium oxide content (No2O) and/or lithium oxide content (U2O), in the range from 5% (percent by mass) to 20% (percent by mass), in particular in the range from 10% ( Mass percent) to 14.5% (mass percent) or in the range of 12% (mass percent) to 13.5% (mass percent).
• alkali oxide content in particular sodium oxide content (No2O) and/or lithium oxide content (U2O)
• No2O sodium oxide content
• U2O lithium oxide content
• the glass material can (alternatively or additionally) advantageously have a potassium oxide (K2O) content of at most 7% (percent by mass), in particular at most 3% (percent by mass) or at most 1% (percent by mass).
• K2O potassium oxide
• the glass material can have a potassium oxide content in the range from 0.5% (percent by mass) to 0.9% (percent by mass).
• the glass material has a boron trioxide content (B2O3) of less than 15% (percent by mass), in particular of at most 5% (percent by mass).
• B2O3 boron trioxide content
• a glass article according to the invention process has particularly good strength values, although it can be made of an inexpensive glass material.
• a strength of the glass object in particular a strength measured according to DIN EN 1288-5, can be achieved which is at least 1.5 times, in particular at least twice or at least three times or at least four times or at least five times higher than the strength of an identical untreated one Glass object, in particular a glass object of the same shape and size and the same glass material.
• float glass with a thickness of 0.95 mm which is made of alkali-earth-alkaline silicate glass as the glass material
• a treatment according to the invention in which a 30-minute ion exchange process was carried out
• Float glass with a thickness of 0.95 mm is used for displays, for example.
• the average double ring flexural strength for the samples of untreated float glass was 550 MPa
• the average double ring flexural strength for the samples treated according to the invention was 1,600 MPa.
• strength values can be achieved which are at least comparable to the strength of conventional display glasses (in particular display glasses made from special glass and treated with more complex conventional methods).
• the glass object can be designed, for example, as a hollow body, in particular a drinking glass, a vase, a mug, a bowl or a bottle. It is also possible for the glass object to be designed as a crockery object, in particular as a plate or platter.
• the glass object can also be in the form of flat glass, for example for a flat screen.
• FIG. 2 shows a representation of the temperature conditions when carrying out an exemplary embodiment of a method according to the invention.
• FIG. 1 schematically shows a representation, not true to scale, of the temperature conditions during the implementation of the method according to the invention for increasing the strength, in particular the transverse rupture strength, of a glass article made of a glass material.
• the glass object is heated 1 from an initial temperature TA, which can be room temperature, for example, to a first temperature Ti, which is above the transformation temperature T g of the glass material of the glass object.
• the first temperature Ti is preferably in a first range 3 from 100 Kelvin to 300 Kelvin above the transformation temperature T g of the glass material.
• the glass object is shock-cooled 2 to a second temperature T2, which is below the transformation temperature T g of the glass material.
• the second temperature is preferably in a second range 4 from 50 Kelvin to 200 Kelvin below the transformation temperature T g .
• the chilling 2 is performed by contacting a cooling means having the second temperature T2 and which is at the same time also an exchange means for the third step (not shown) of performing an ion exchange process at the second temperature T2.
• the ion exchange process is preferably carried out for a period of time in the range from 15 minutes to 300 minutes, in particular in the range from 20 minutes to 40 minutes, in particular for about 30 minutes.
• Fig. 2 schematically shows a representation of the not true to scale Temperature conditions during the execution of an embodiment of a method according to the invention for increasing the strength, in particular the transverse rupture strength, of a glass article made from soda-lime glass.
• the glass object is heated 1 from an initial temperature TA, which can be 20 °C, for example, in a furnace (not shown) to a first temperature Ti of 745 °C, which is above the transformation temperature T g of 530 °C of the glass material of the glass article.
• an initial temperature TA which can be 20 °C, for example, in a furnace (not shown)
• a first temperature Ti of 745 °C, which is above the transformation temperature T g of 530 °C of the glass material of the glass article.
• the glass object is immediately shock-cooled 2 to a second temperature T2, which is 420°C.
• Shock cooling 2 is carried out by immersing the glass object in a cooling bath (not shown) which contains a molten salt of potassium nitrate as a cooling agent.
• the molten salt has a temperature of 420 °C.
• the molten salt is at the same time also the exchange medium for the third step (not shown) of carrying out an ion exchange process, which is carried out at the second temperature T2 of 420°C.
• the glass object is left in the molten salt for a period of time in the range from 15 minutes to 300 minutes, in particular in the range from 20 minutes to 40 minutes, in particular for about 30 minutes.
• the glass article is taken out from the cooling bath and further cooled down to room temperature in a cooling position outside the cooling bath and finally cleaned.

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• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Organic Chemistry (AREA)
• Physics & Mathematics (AREA)
• Thermal Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Geochemistry & Mineralogy (AREA)
• Surface Treatment Of Glass (AREA)
• Re-Forming, After-Treatment, Cutting And Transporting Of Glass Products (AREA)
• Glass Compositions (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=73040197

Family Applications (1)

Country Status (11)

Family Cites Families (7)

• 2020
  • 2020-09-03 LU LU102043A patent/LU102043B1/de active IP Right Grant
• 2021
  • 2021-09-02 AU AU2021335528A patent/AU2021335528A1/en active Pending
  • 2021-09-02 WO PCT/EP2021/074281 patent/WO2022049203A1/de unknown
  • 2021-09-02 US US18/024,349 patent/US20230312388A1/en active Pending
  • 2021-09-02 CN CN202180063039.6A patent/CN116234780A/zh active Pending
  • 2021-09-02 JP JP2023515036A patent/JP2023539777A/ja active Pending
  • 2021-09-02 EP EP21770233.1A patent/EP4208421A1/de active Pending
  • 2021-09-02 KR KR1020237010177A patent/KR20230061419A/ko unknown
  • 2021-09-02 MX MX2023002582A patent/MX2023002582A/es unknown
  • 2021-09-02 CA CA3193626A patent/CA3193626A1/en active Pending
  • 2021-09-02 TW TW110132609A patent/TW202220944A/zh unknown

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