The present invention relates to a thermochromic glass material comprising heavy metal oxide, alkali oxide, halide and at least one of some other compounds supporting glass formation together with tellurium oxide (TeO2) and a production method thereof.
Thermochromism is the reversible or irreversible change in optical properties of the material with the effect of temperature. Continuous color change observed gradually in the material depending on the changing temperature is called continuous thermochromism; whereas discontinuous thermochromism is the color change occurring in the material at a determined transition temperature as a result of a structural transition which is experienced.
Until today, there are limited number of studies concerning glasses with thermochromic properties and thermochromic property mechanism of the glasses, apart from glasses exhibiting thermochromic properties with thin film coatings made on the glass.
In studies concerning thermochromic glasses; Abe et. al. determined that phosphate glasses change color as a result of phase transition of the phosphorus present as colloidal particles in glass structure with changing temperature, and this transition exhibits reversible properties.1 Kawashima et. al. determined the thermochromic transition temperatures of phosphate glasses.2 Sen et. al. determined that Bi2O3 addition in borate glasses causes reversible thermochromic property since ions are highly polarized with increasing temperature and Bi2O3 ratio.3 Chen et. al. determined that Bi2O3—CdO—Al2O3 glasses exhibit reversible thermochromic property depending on Bi2O3 ratio and bonds are polarized and weaken with increased Bi2O3 ratio, and optical band gap narrows and the absorption edge is shifted to higher wavelengths.4 Chen et. al. determined that Bi2O3—Li2O glasses exhibit thermochromic property, and temperature coefficient of the optical absorption edge of glasses increases with the increased Bi2O3 ratio.5 Bahgat et. al. determined that lead oxide glasses comprising WO3 exhibit thermochromic behaviour.6 1 Abe, Y., Kawashima, K. ve Suzuki, S. Thermochromism in reduced phosphate glasses. Journal of the American Ceramic Society, 64, 206-209, 1981.2 Kawashima, K, Ding, J., Hosono, H. and Abe, Y. DTA studies for thermochromism and thermal bleaching in reduced phosphate glasses. The Ceramic Society of Japan, 97, 823-827, 19893 Sen, A., Kumar, J. ve Chakravorty, D. Thermochromism in borate glasses containing bismuth oxide. Journal of Materials Science Letters, 2, 677-679, 19834 Chen, D., Miura, Y., Nanba, T. and Osaka, A. Thermochromism and temperature dependence of the energy gap in cadmium aluminum bismuthate glasses. Journal of the Ceramic Society of Japan, 104, 79-83, 19965 Chen, D. P., Jiang, X. W. and Zhu, C. S. Study on the thermochromic properties of Bi2O3—Li2O glasses. Acta Physica Sinica, 50, 1501-1506, 20016 Bahgat, A. A., El-Samanoudy, M. M. and Sabry, A. I. Optical and electrical properties of binary WO3—Pb3O4 glasses. Journal of Physics and Chemistry of Solids, 60, 1921-1931, 1999
In addition to these, Japanese Patent document no JP2735147B2, an application known in the state of the art, discloses to obtain a thermochromic material whose optical characteristics vary automatically and reversibly in accordance with the environmental temperature in vanadium dioxide film containing tungsten by a reactive binary simultaneous sputtering. Since the material causes semi-conductive metal phase transition, its infrared transmittance automatically changes with the changing temperature.
Japanese Patent document no JP08040749A, another application known in the state of the art, discloses thermochromic glass avoiding shading in color due to the deterioration of optical properties and extremely resistant to weather conditions, and the production method thereof. Furthermore, several metal oxides that can be used in the thermochromic glass are disclosed in detailed description part.
Li et. al. determined that there is a reversible shift in absorption bands of silicate, borosilicate and phosphosilicate glasses containing 80% and above PbO and TeO2 by weight with changing temperature, and thermochromic property is caused by increased temperature and increase in Pb2+ and Te4+ bond polarization together with PbO and TeO2 ratio.7 Inoue et. al. determined that absorption edge of TeO2—Na2O, TeO2—Fe2O3, B2O3—PbO and PbO—SiO2 glasses containing transition metal oxide is shifted towards the red wavelength in the optical spectrum with increasing temperature and these glasses exhibit reversible thermochromic property in visible region.8 7 Li, G., Nogami, M. and Abe, Y. Temperature and compositional dependence of optical absorption edge in glasses containing PbO and TeO2. Journal of Materials Research, 9, 2319-2322, 19948 Inoue, S., Shimizugawa, Y., Nukui, A. and Maeseto, T. Thermochromic property of tellurite glasses containing transition metal oxides. Journal of Non-Crystalline Solids, 189, 36-42, 1995
Even though the previous art discloses glasses containing tellurium oxide, no glass or glass production method exhibiting thermochromic property by means of tellurium oxide directly contained therein is disclosed. In thermochromic glasses containing tellurium oxide known in the technique, the said thermochromic property is provided via the semi-conductivity of transition metals, polarization ability of metal ions or bond polarization in these glasses.
The objective of the present invention is to provide a semi-conductive thermochromic glass material.
Another objective of the present invention is to provide a reversible thermochromic glass material.
A further objective of the present invention is to provide a thermochromic glass material containing tellurium oxide.
Yet another objective of the present invention is to provide a production method for thermochromic glass material which has the abovementioned features.
The figures of the inventive thermochromic glass material and a production method thereof are as follows:
The inventive thermochromic glass material essentially comprises at least one of heavy metal oxide, alkali oxide, halide components together with tellurium oxide (TeO2) in order to achieve glass formation.
In the preferred embodiment of the invention, the glass material comprises at least one of WO3, Li2O, Na2O, K2O, ZnO, CdO, B2O3, TiO2, CuO, Fe2O3, V2O5, PbO, Nb2O5, MoO3, GeO2, P2O5, Ag2O, Sb2O3, PbF2, LiCl, ZnCl2 compounds as well as TeO2 in ratio of 30-95% by mole, the ratios of the said compounds in the composition are 0-35%, 0-45%, 0-40%, 0-30%, 0-40%, 0-15%, 0-27.5%, 0-15%, 0-50%, 0-20%, 0-55%, 0-20%, 0-25%, 0-55%, 0-30%, 0-25%, 0-20%, 0-20%, 0-25%, 0-30%, 0-30% by mole, respectively.
The inventive glass material allows electronic passages by behaving like a conductive electrolyte. The transmittance and absorption edge values of the material in the visible region change with the temperature (
In one embodiment of the invention, the ratios of the compounds inside the thermochromic glass are 50% TeO2, 25% WO3, 25% Li2O by mole. According to this embodiment of the invention, the changes in transmittance and absorption edge values with temperature are given in
A thermochromic glass material production method (100) developed to fulfill the objective of the present invention comprises the steps of
In the inventive method (100), first the content of the powder mixture to be mixed is determined, and each component to be in the mixture are weighed and mixed with each other homogenously (101).
While preparing the powder mixture (101), in order to obtain Li2O, Na2O, K2O and B2O3 components in the final product, Li2CO3, Na2CO3, K2CO3 and H3BO3 are used as starting materials. The carbonates and hydrates which are used are degraded during melting and they transform into oxide.
In the preferred embodiment of the invention, the mixture is placed into a furnace preheated to 750-900° C. within a crucible with lid manufactured from platinum or gold in order to heat and melt. It is enabled to be molten by waiting for 30-60 minutes in the determined temperature range (102).
Cooling and shaping the mixture after melting can be performed in various ways. In one embodiment of the invention, in order to prevent the molten glass mixture from suddenly cooling and cracking during pouring into a mold, first the mixture is poured into a stainless steel or bronze mold preheated to 200-250° C. (103).
The glass material poured into a mold is kept for 60-120 minutes in a drying oven heated to 200-300° C., and then it is cooled to room temperature in a controlled way (104). With controlled and slow cooling performed in this way, internal stresses are eliminated.
The change in optical features of the obtained glass samples in thickness of 1-3 mm in the visible region was measured with a UV-Vis spectrophotometer having an in-situ heating unit. Measurements were performed for temperatures selected between the room temperature and glass transition temperature. The changes in the visible region spectra obtained depending on temperature are determined in %, transmittance or absorption; the optical band gap energy values of the glasses were measured depending on the temperature with calculations made on the said changes.
In another analysis made on the inventive thermochromic glass materials, the glass surfaces were made conductive with silver dye, and their electrical conductivity was measured depending on the temperature. The analyses which were performed have shown that the conductivity values of the inventive telluride glasses increase with the increased temperature, their conductivity changes reversibly with temperature, and they have semi-conductive feature. The thermochromic property shown by the telluride glasses is originated from their semi-conductive behavior.
As a result of the analyses which were made, the material comprising TeO2—WO3—A2O (A: Li, Na, K) has given the best result in terms of transmittance, absorption edge, conductivity change, thermochromic property and reversible thermochromic behavior depending on temperature.
The inventive telluride glasses showing thermochromic property can be used in permeable filters used in optical and spectroscopic analysis devices and color measurement devices, calibration apparatuses, microelectronic applications, temperature sensors and data storage devices.
Number | Date | Country | Kind |
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2014/05119 | May 2014 | TR | national |
Filing Document | Filing Date | Country | Kind |
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PCT/TR2015/000193 | 5/6/2015 | WO | 00 |