Patent Application
20070045555
The present invention relates to scintillating glasses which emit light efficiently when exposed to radiation, such as X-rays.
Substances that efficiently emit fluorescence in response to excitation by light, heat, radiation, etc. are called “fluorescent substances”. Particularly, fluorescence emission in response to radiation, such as X-rays, γ-rays or charged particles, is called “scintillation”, and substances that emit scintillation light are called “scintillators”.
Today, scintillators are used extensively in medical diagnosis devices, such as X-ray CT devices, PET (Positron Emission Tomography) devices and nondestructive test devices using radiation rays, electromagnetic calorimeters for high-energy physics experiments, etc. Various characteristics, such as a high atomic number, high density, high light yield amount, high transparency in emission wavelengths, short decay time and high radiation resistance, are required for scintillators used for such purposes.
Of such characteristics or properties, the atomic number and density are very important in that they not only relate to an absorption factor of radiation and contribute to minitualization of a detector using the glass but also enhance the resolution of irradiated positions. In X-ray and PET devices where the radiation energy is relatively low, the absorption factor is proportional to the fourth power of the atomic number, while, in cases where the radiation energy is extremely high, the absorption factor is proportional to the atomic number. In any event, the scintillators are required to have a great atomic number and high density. In addition to the aforementioned characteristics or properties, it is desirable that the scintillator can be manufactured at low cost, formed into a large size and formed into any one of various shapes with ease.
Presently, there are known a great number of inorganic scintillators, such as single crystal, ceramic and glass scintillators. Scintillating glasses are advantageous in that they not only have high transparency but also can be readily formed into any desired shape, such as a fiber shape, although they have lower emission efficiency; thus, scintillating glasses have been under strenuous study. U.S. Pat. Nos. 3,654,172, 5,122,671 and 5,391,320, for example, disclose scintillating glasses using Tb as an activator agent. However, these scintillating glasses, each of which is based on alkaline-earth silicate, have low density and thus are considerably limited in application.
In view of the foregoing, it is an object of the present invention to provide an improved scintillating glass which is stable in practical use and achieves both high density and high emission efficiency.
The inventor has come to achieve the present invention by setting a composition of glass components to a particular novel range with a view to providing a dense glass, especially scintillating glass.
Namely, a preferred embodiment of the present invention can be provided by any one of the following arrangements.
(Arrangement 1) A glass or scintillating glass which comprises Tb2O3 and/or Eu2O3, and wherein a content of at least one of Tb2O3 and Eu2O3 is 0.0 1 to 15 mol percent on the oxide basis, the glass or scintillating glass containing none of Ga2O3 and GeO2 and having a density of 3.0 g/cm3 or over.
(Arrangement 2) A glass or scintillating glass as defined in Arrangement 1 which further comprises F wherein a total amount of F calculated on the assumption that a part or whole of oxides of the glass has been substituted by a fluoride is 1 to 100 mol % to a total amount of components of the glass expressed on the oxide basis.
(Arrangement 3) A glass or scintillating glass as defined in Arrangement 1 or 2 which further comprises Gd2O3 and/or Lu2O3, and wherein a content of at least one of Gd2O3 and Lu2O3 is 0.1 to 50 mol percent on the oxide basis.
(Arrangement 4) A glass or scintillating glass as defined in any one of Arrangements 1-3 which further comprises, in mol percent on the oxide basis, 30 % to 70 % (SiO2+B2O3) and/or 0 to 35 % Al2O3.
(Arrangement 5) A glass or scintillating glass as defined in any one of Arrangements 1-4 which further comprises, in mol percent on the oxide basis, 0 to 10 % P2O5.
(Arrangement 6) A glass or scintillating glass as defined in any one of Arrangements 1-5 which further comprises, in mol percent on the oxide basis, 0% to 30% (Y2O3+La2O3) and/or 0 to 60 (RO+Rn2O), and/or 0 to 5% (As2O3+Sb2O3), and/or 0 to 15 M2O3, and in which R is at least one component selected from the group consisting of Mg, Ca, Sr, Ba and Zn, Rn is at least one component selected from the group consisting of Li, Na, K and Cs, and M is at least one component selected from the group consisting of Ce, Nd, Pr, Sm, Dy, Ho, Er, Tm, Yb, Mn, Bi and Cr.
(Arrangement 7) A glass or scintillating glass as defined in any one of Arrangements 1-6 wherein a decay time is 5 μs or below.
(Arrangement 8) A glass or scintillating glass as defined in any one of Arrangements 1-7 which emits light in response to excitation with radiation and is used as a scintillator.
(Arrangement 9) A radiation meter device which uses the glass or scintillating glass as recited in any one of Arrangements 1-8.
(Arrangement 10) A CT device which uses the glass or scintillating glass as recited in any one of Arrangements 1-8.
The component compositions of the present invention are expressed in mol percent above, and they may not be suitably defined directly in mass percent representation. However, it should also be noted that the component compositions of the present invention may alternatively be defined as follows, using mass percent representation, and these alternatives can accomplish similar advantageous results to the aforementioned.
(Arrangement 11) A glass or scintillating glass which comprises Tb2O3 and/or Eu2O3, and wherein a content of at least one of Tb2O3 and Eu2O3 is 0.01 to 20 mass percent on the oxide basis, the glass or scintillating glass containing none of Ga2O3 and GeO2 and having a density of 3.0 g/cm3 or over.
(Arrangement 12) A glass or scintillating glass as defined in Arrangement 11 which further comprises F wherein a total amount of F calculated on the assumption that a part or whole of oxides of the glass has been substituted by a fluoride is 0.5 to 20 mass % to a total amount of components of the glass expressed on the oxide basis.
(Arrangement 13) A glass or scintillating glass as defined in Arrangement 11 or 12 which further comprises Gd2O3 and/or Lu2O3, and wherein a content of at least one of Gd2O3 and Lu2O3 is 0.5 to 90 mass percent on the oxide basis.
(Arrangement 14) A glass or scintillating glass as defined in any one of Arrangements 11-13 which further comprises, in mass percent on the oxide basis, 3% to 60% (SiO2+B2O3) and/or 0 to 20% Al2O3.
(Arrangement 15) A glass or scintillating glass as defined in any one of Arrangements 11-14 which further comprises, in mass percent on the oxide basis, 0 to 15% P2O5.
(Arrangement 16) A glass or scintillating glass as defined in any one of Arrangements 11-15 which further comprises, in mass percent on the oxide basis, 0 to 50% (Y2O3+La2O3) and/or 0 to 60% (RO+Rn2O), and/or 0 to 5% (As2O3+Sb2O3), and/or 0 to 10% M2O3, and in which R is at least one component selected from the group consisting of Mg, Ca, Sr, Ba and Zn, Rn is at least one component selected from the group consisting of Li, Na, K and Cs, and M is at least one component selected from the group consisting of Ce, Nd, Pr, Sm, Dy, Ho, Er, Tm, Yb, Mn, Bi and Cr.
According to the present invention, there can be provided a glass or scintillating glass with a density of 3.0 g/cm3 or over, which is thermally stable against to crystallization and scintillate in response to excitation with X-ray radiation. Further, according a more preferred embodiment of the present invention, there can be provided a glass or scintillating glass having a density of 3.6 g/cm3 or over.
Further, the glass of the present invention can achieve a decay time of 5 μs or below. In this specification, the terms “decay time” are used to refer to a length of time in which light emission intensity of a monitored maximum emission peak wavelength falls to 1/e (36.8%) after termination of the excitation.
The following will describe embodiments of the present invention, but it should be appreciated that the present invention is not limited to the described embodiments and various modifications of the invention are possible without departing from the basic principles. The scope of the present invention is therefore to be determined solely by the appended claims.
For better understanding of the objects and other features of the present invention, its preferred embodiments will be described hereinbelow in greater detail with reference to the accompanying drawings, in which:
The following paragraphs describe reasons why the composition of the glass of the present invention is limited as set forth above. Unless stated otherwise, contained amounts or contents of individual components of the glass will be represented in mol (or mole) percent on the oxide basis.
SiO2 and B2O3 are glass-forming oxides, which are components useful for providing stable glass. In order to provide more stable glass, the lower limit of the content of at least one of these components, SiO2 and B2O3, is set preferably at 30%, more preferably at 35% and most preferably at 40%. Further, in order for the glass to achieve desired high density, the upper limit of the content of at least one of these components is set preferably at 70%, more preferably at 65% and most preferably at 60%. It is preferable to contain both of the two components, in order to achieve the aforementioned advantages. However, of these two components, B2O3 performs a negative function of lowering the emission intensity although it is effective in enhancing the meltability and stability of glass; thus, it is preferable to minimize the content of B2O3. Further, the ratio, by mol percent, of SiO2 to B2O3 (SiO2/B2O3) is set preferably at 0.2 or over, more preferably at 0.5 or over, and most preferably at 1.0 or over.
Gd2O3 and Lu2O3 are components that greatly contribute to enhancement of not only the density but also the light emission of glass and thus greatly contribute to accomplishment of the object of the present invention. Therefore, it is preferable to contain at least one of these two components. If the lower limit of the total content of these two components is less than 0.1%, it tends to be difficult to achieve the aforementioned advantages to a sufficient degree. Therefore, the lower limit of the content of at least one of these two components is set preferably at 0.1%, more preferably at 1% and most preferably at 3%. Further, if the total content of these two components exceeds 50%, the stability of the glass tends to greatly lower; thus, the upper limit of the content of at least one of these components is set preferably at 50%, more preferably at 45% and most preferably at 40%.
The upper limit of the content of Gd2O3 alone is most preferably 25% from the viewpoint of the light emission amount.
It is preferable that Lu2O3 be added because Lu2O3 is effective in enhancing the density of glass. However, adding a great amount of Lu2O3 would present a cost problem since the raw material of Lu2O3 is costly. Therefore, it is most preferable to contain both of the two components. In the case where both of Gd2O3 and Lu2O3 are contained, the ratio, by mol percent, of Lu2O3 to (Gd2O3+Lu2O3) is set preferably at 0.005 or over.
Further, La2O3 or Y2O3 is a component that is effective in enhancing the stability and density of glass and thus may be added as desired. However, in order to maintain good stability of the glass, the upper limit of the total content of these components is set preferably at 30%, more preferably at 20% and most preferably at less than 4%.
Al2O3 is a component effective in enhancing the meltability and stability, and thus, it may be added as desired. In order to maintain good stability of the glass, the upper limit of the content of this component is set preferably at 35%, more preferably at 30% and most preferably at less than 25%. Further, in order to effectively achieve the aforementioned advantages, the lower limit of the content of this component is set preferably at 0.1%, more preferably at 0.5% and most preferably at 1%. Whereas the material of Al2O3 may be introduced in the form of Al(OH)3, it is especially effective to introduce the material in the form of AlF3.
Further, RO or Rn2O (here, R is at least one component selected from the group consisting of Zn, Ba, Sr, Ca and Mg, and Rn is at least one component selected from the group consisting of K, Na, Li and Cs) is a component that is effective in enhancing the meltability and stability of glass and thus may be added as desired. If the total content of these components exceeds 60%, the stability of the glass would lower; thus, the upper limit of the content is set preferably at 60%, more preferably at 55% and most preferably at 40%. Besides, in order to attain the aforementioned advantages more effectively, the lower limit of the content of these components is set preferably at 1% and most preferably at 5%. Of these components, BaO is the most effective in enhancing the stability and density of the glass, and it is preferable to contain BaO.
P2O5 is a component that may be added as desired and is effective in enhancing the stability of glass. Especially, P2O5 is useful for maintaining a luminescent ion Tb3+ in this state as will be later described. Thus, in order to attain the respective advantages to a sufficient degree, the lower limit of the content is set preferably at 0.1% and most preferably at 1%. Preferable upper limit of the content is 10%, beyond which the stability of the glass would rather deteriorate. More preferable upper limit of the content is 8%, and the most preferable upper limit of the content is 6%.
F is a component effective in lowering the melting point of glass and enhancing the meltability and stability of glass. F can also serve as a reducing agent for maintaining the luminescent ion Tb3+ in this state as will be later described. Further, because a fluorine ion binds with a luminescent ion, F also serves to produce an effect of contributing to enhancement of the light emission characteristic. Further, it is preferable that the content of F, intended to attain the aforementioned effects, be set as follows. Namely, the lower limit of the total amount, relative to the total amount of the components represented on the oxide basis, of F calculated on the assumption that a part or whole of oxides of the glass has been substituted by a fluoride is set preferably at 1 mol %, more preferably at 5 mol % and most preferably at 10%, while the upper limit of the content of F is set preferably at 100 mol %, more preferably at 95 mol % and most preferably at 90%.
In this specification, the phrase “represented on the oxide basis” is used, assuming that oxides, complex salts, metal fluorides, etc., used as raw materials of the components of the glass composition of the present invention, have all been decomposed and converted to oxides during the melting process, to refer to the manner of expressing each converted oxide in mol percent.
Further, the phrase “total amount of F calculated on the assumption that a part or whole of oxides of the glass has been substituted by a fluoride” is used herein to refer to a mol % expressed by the number of moles of F when calculated as the F atom of a total content of F, which can exist in the form of one or more metal fluorides etc. in the glass composition of the present invention, relative to the total number of moles of the composition expressed on the oxide basis.
Similarly, in the case where the composition is expressed on the basis of percent by mass (or mass percent), the phrase “represented on the oxide basis” is used, assuming that oxides, complex salts, metal fluorides, etc., used as raw materials of the components of glass composition of the present invention, have all been decomposed and converted to oxides during the melting process, to refer to the manner of expressing each converted oxide in mass percent. Further, the phrase “total amount of F calculated on the assumption that a part or whole of oxides of the glass has been substituted by a fluoride” is used herein to refer to a mass % expressed by the mass of F when calculated as the F atom of a total content of F, which can exist in the form of one or more metal fluorides etc. in the glass composition of the present invention, relative to the total mass of the composition expressed on the oxide basis.
These representations pertaining to the F component are commonly called “outer percentage” in Japan.
The Tb3+ ion or Eu3+ functions as an emission or luminescence center and is essential for achieving the scintillation property of the glass of the present invention. Such an ion can be introduced in the form of Tb2O3, Tb4O7, Eu2O3 or fluoride. In the case where the ion is introduced in the form of Tb2O3 or Eu2O3, the lower limit of the content is set preferably at 0.005%, more preferably at 0.01% and most preferably at 0.05%, in order to provide a sufficient light emission intensity. However, because the light emission intensity would dramatically lower if concentration quenching occurs, the upper limit of the content is set preferably at 15%, more preferably at 12% and most preferably at 8%.
In order to increase the light emission of the above-mentioned luminescent ion, it is possible to add, as sensitizers, Ce2O3, Nd2O3, Pr2O3, Sm2O3, Dy2O3, Ho2O3, Er2O3, Tm2O3, Yb2O3, Mn2O3, Bi2O3, Cr2O3, etc. However, the maximum total amount of these components should be restricted so as not to exceed 15 mol %; adding these sensitizers beyond 15 mol % would rather decrease the light emission. More preferable amount of the components is 10% or below, and the most preferable amount is 5 mol % or below. Note that these ions may be introduced into the glass in the form of fluorides or chlorides rather than in the form of the above-mentioned oxides. Whereas cations of some of the aforementioned oxides take valences other than the above-mentioned, they are represented in terms of the aforementioned oxides in the present invention.
As2O3 or Sb2O3 is a component that functions also as a fining agent during melting of the glass or as a reducing agent to allow the above-mentioned Tb3+, functioning as the above-mentioned emission or luminescence center, to remain in this state, and that may be added as desired. If the total amount of either or both of these components exceeds 5%, the light emission property tends to remarkably decrease. Further, if the total amount of either or both of these components is 0.005% or below, the achievable advantages tend to be insufficient. Thus, in order to readily achieve the aforementioned advantages, the total amount of either or both of these components is set preferably to a range of 0.005-5%, more preferably to a range of 0.01-3% and most preferably to a range of 0.01-2%. Sb2O3 is also effective as a reducing agent and As2O3 is an undesirable component from an environmental viewpoint, and thus, it is preferable that As2O3 be not contained and Sb2O3 alone account for the content in any one of the aforementioned ranges.
With the glass of the present invention, each of transitional metal components having an absorption property in the visible range, such as V, Fe, Co and Ni, can not achieve a good scintillator property even when it is introduced into the glass, and thus, it is preferable that such a component be not substantively contained.
Further, there has recently been a tendency to avoid use of Pb as being a harmful chemical substance, and thus, it is preferable that Pb be not contained because environmental measures are required not only in the glass making step but also in the processing step and even disposal after productization.
Too much content of Ga2O3 and GeO2 would lower the light emission property. Further, because the raw materials of Ga2O3 and GeO2 are costly, it is preferable that these components be not contained from the viewpoint of the cost as well.
In this specification, the phrase “does not substantively contain” means that one or more other components may be contained only within a range where they do not impair various properties of the glass. In order to prevent the various properties of the glass of the present invention from being impaired, it is more preferable to not artificially contain other components except where such other components are contained as impurities.
The high-density scintillating glass of the present invention can be made in the following manner. Namely, predetermined amounts of individual starting materials are weighed and mixed uniformly, after which they are put in a platinum, quartz or alumina crucible or the like and melted within an electric furnace at 1,200-1,550° C. for two to ten hours. After that, the resultant glass melt is poured into a mold and formed into a predetermined shape, so that a desired glass can be provided.
The following paragraphs describe the present invention using various specific examples; however, it should be appreciated that the present invention is never limited to these examples.
Staring materials, SiO2, BaO, MgO, Li2O, AlF3, GdF3 and Tb2O3, were weighed to provide a composition of 50SiO2-2OBaO-5MgO-10Li2O-6AlF3-6GdF3-3Tb2O3 in mol percent (not on the oxide basis) and then mixed uniformly, after which they were melted in a platinum crucible at 1,420° C. for two hours. After that, the glass melt was cast onto a pre-heated stainless plate to thereby make a plate-shaped glass. The thus-provided glass was polished and then subjected to measurement of various properties. Green light emission was observed, with the naked eye, in both of a case where the excitation was by ultraviolet rays and a case where the excitation was by X-rays.
Glass was made which comprised a composition of 50SiO2-24BaO-7MgO-12Li2O-3K2O-2Al2O3-2Tb2O3 in mol percent with none of AlF3 and GdF3 contained.
Example 2-Example 8 were made in a similar manner to Example 1. Table 1 and Table 2 show glass compositions in mol percent (not on the oxide basis), densities and amounts of light emission responsive to X-ray excitation of Examples 1-8 and Comparative Example 1. Table 3 and Table 4 show glass compositions in mol percent on the oxide basis, densities and amounts of light emission responsive to X-ray excitation of Examples 1-8 and Comparative Example 1. Note that the light emission amount of the glass of the present invention was indicated as a relative value to the light emission amount of Comparative Example 1 that was assumed to be “100”. From Table 1, it can be seen that the glass of the present invention has higher density and greater amount of light emission.
Glass was made in a similar manner to Example 1, which comprised a composition of 35SiO2-15B2O3-20AlF3-29.8Gd2O3-0.2Eu2O3 in mol percent (not on the oxide basis) (in mol percent on the oxide basis, 38.9SiO2-16.7B2O3-11.1Al2O3-33.1Gd2O3-0.2Eu2O3+66.7% F (“outer percentage”)). The thus-made glass has a density of 5.40 g/cm3, and with this glass, green light emission was observed, with the naked eye, in both of a case where the excitation was by ultraviolet rays and a case where the excitation was by X-rays.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2005-250763 | Aug 2005 | JP | national |
