Glass composition formulated for a glass-metal bond of a tube collector and glass-metal bond made with glass of said glass composition

Information

  • Patent Grant
  • 8178451
  • Patent Number
    8,178,451
  • Date Filed
    Friday, September 11, 2009
    15 years ago
  • Date Issued
    Tuesday, May 15, 2012
    12 years ago
Abstract
The glass-metal bond for a tube collector includes a glass tube and metal part bonded to the glass tube. In order to match the thermal expansion properties, the glass tube has the following composition: SiO2, 73-77 wt. %; B2O3, 6-<8 wt. %; Al2O3, 6-6.5 wt. %; Na2O, 5.5-7 wt. %; K2O, 1-3 wt. %; CaO, 0.5-3.2 wt. %; MgO, 0-2 wt. %; Fe2O3, 50-150 ppm; and TiO2 0-<100 ppm. The ratio of the sum of the alkaline-earth metal oxides (in mol %) to the sum of the alkali metal oxides (in mol %) is ≦0.6. The metal part is preferably made of metal material no. 1.3981 according to DIN 17745. The glass composition itself is also part of the invention.
Description
CROSS-REFERENCE

The invention described and claimed herein below is also described in German Patent Application 10 2008 047 280.8, filed Sep. 16, 2008 in Germany. The aforesaid German Patent Application provides the basis for a claim of priority of invention for the invention claimed herein below under 35 U.S.C. 119 (a)-(d).


BACKGROUND OF THE INVENTION

1. The Field of the Invention


The invention relates to a glass-metal bond made with glass having a composition that meets the requirements of glass-metal bonds, and particularly of tube collectors used in a solar energy collection apparatus. The invention also relates to the glass that is formulated with a composition that meets the requirements of the glass-metal bonds.


2. Description of the Related Art


Glass-metal bonds are used, for example, in vacuum tube collectors. In vacuum tube collectors, a vacuum-tight glass-metal bond between the absorber tube consisting of a metal and the envelope tube consisting of glass is required for thermal insulation.


Such tube collectors are used, for example, in parabolic trough solar power plants.


In parabolic trough solar power plants, operating temperatures of up to 400° C. are generated in the collectors with strong local temperature differences. In addition, temperature changes caused by the diurnal cycle and intermittent cloudy periods produce continual stresses.


In high-temperature solar collectors, on the one hand, so-called unmatched glass-metal bonds have been used to date. They are called unmatched glass-metal bonds because the glass and metal have different coefficients of thermal expansion. On the other hand, so-called matched glass-metal bonds are used, in which case one possible way of achieving the match is to use a plurality of intermediate glasses. This approach, however, has various disadvantages.


DE 10 2004 008 559 A1 discloses a glass-metal bond of a tube collector, which uses an aluminum borosilicate glass that is also employed as a material for primary pharmaceutical packaging. It is not specially adapted to the requirements of a glass for tube collectors and to the requirements of producing such a glass. A similar glass composition range of a glass, in particular for solar thermal applications, is described in DE 10 2006 041 469 B3. DE 44 30 710 C1 discloses low-boron borosilicate glasses which have a coefficient of thermal expansion α20/300≦5.3×10−6/K.


The receiver, as the key part of a tube collector for a parabolic trough solar power plant, consists of an inner tube made of steel and an outer envelope tube made of glass. The two components must be connected vacuum-tightly by means of glass-metal bonds.


The steel tube (absorber tube) is coated with a radiation-selective material, in order to ensure a high absorption ratio.


The envelope tube requires a coefficient of thermal expansion matched to the metal.


The vacuum between the envelope tube and the absorber tube reduces the heat loss and makes a contribution to optimal heating efficiency.


The envelope tube is provided with an antireflection layer which, together with the requisite high transmission of the glass, is intended to give a high transmissivity of at least 96%.


The envelope tube requires high thermal and temperature change stability, high weather resistance, i.e. a high hydrolytic stability, and high mechanical stability, i.e. high strength.


Despite its high load-bearing capacity, in particular thermal load-bearing capacity, it should be readily meltable in the least energy-intensive way possible. All these glass and production properties should furthermore be achievable with the least possible production and raw material costs.


SUMMARY OF THE INVENTION

It is therefore an object of the invention to provide a glass for a matched glass-metal bond of a tube collector, which fulfils the aforesaid requirements of glass-metal bonds.


It is also an object of the invention to provide a glass-metal bond made with the glass according to the invention, which fulfils the requirements for glass-metal bonds, especially for a tube collector of a solar energy collection apparatus.


These objects and others, which will be made more apparent hereinafter, are attained by a glass which contains the following constituents in the following amounts:


















SiO2
73-77
wt. %



B2O3
6-<8
wt. %



Al2O3
6-6.5
wt. %



Na2O
5.5-7
wt. %



K2O
1-3
wt. %



CaO
0.5-3.2
wt. %



MgO
0-2
wt. %



Fe2O3
50-150
ppm



TiO2
0-<100
ppm,










wherein the ratio of the sum of the amounts of the alkaline-earth metal oxides (RO), in mol %, to the sum of the amounts of the alkali metal oxides (R2O), in mol %, is ≦0.6, and by its use for a glass tube in a tube collector comprising a glass-metal bond.


The limitation to a comparatively small content of CaO assists in attaining a desired low melting temperature.


Setting the desired low coefficient of thermal expansion is facilitated by the aforesaid ratio, ΣRO (mol %)/ΣR2O (mol %).


Similar, relatively low-boron glasses are already known from DE 100 35 801 A for use as primary packaging, for example for syringes, carpules, vials and test tubes. The production of such primary pharmaceutical packaging is based on glass tubes with a maximum outer diameter of 30 mm. Similar glasses, which are likewise processed only to form tubes with very small diameters, namely backlights, are also known from DE 10 2004 027 120 A1 and DE 10 2004 027 119 A1.


The use of such low-boron glasses to produce glass tubes for solar thermal applications, which must have a diameter of more than 120 mm, and for use in glass-metal bonds, has not been considered in the past. This is attributable to the fact that it was not previously realized that these glasses combine properties which are more suitable for use in vacuum tube collectors than those of previously used glasses.


The glasses according to the invention have a coefficient of thermal expansion >5.3×10−6/K to 5.8×10−6/K, in particular about 5.7×10−6/K, which is essential for their use according to the invention and differs only by about 10% from the coefficients of thermal expansion of customary metals. The glasses are furthermore acid- and alkali-resistant (classes S1 and S2 according to DIN 12116 and DIN ISO 695), and water-resistant (class HGB 1, DIN ISO 719). Furthermore, these glasses can also be readily processed to form tubes with outer diameters >120 mm. These advantageous properties make the use of junction glasses superfluous, so that an industrially automatable production process is possible. They furthermore have low iron content, which is particularly important owing to the transmission requirements for envelope tubes in vacuum tube collectors. The person skilled in the art knows how to achieve the low iron content by selecting suitable low-iron raw materials. The ratio Fe2+/Fe3+ is in this case preferably 0.03-0.1, particularly preferably 0.045-0.055. These ratios are ensured by using sufficient nitrate levels in the batch. For example, about 0.5-1.2 wt. % nitrate is used, preferably 0.8-1.0 wt. %, for example as sodium nitrate or aluminum nitrate.


A glass, which contains the following constituents in the following composition, and its use, are preferred:


















SiO2
73-77
wt. %



B2O3
6.7-7.5
wt. %



Al2O3
6.3-6.5
wt. %



Na2O
5.8-6.8
wt. %



K2O
1-2
wt. %



CaO
2.5-3.2
wt. %



MgO
0.4-1
wt. %



Fe2O3
70-130
ppm



TiO2
0-<100
ppm,










wherein the ratio of the sum of the amounts of the alkaline-earth metal oxides (RO) to the sum of the amounts of the alkali metal oxides (R2O) is ≦0.6.


The glass may be fined with conventional fining agents in conventional amounts. The glass used preferably contains 0.1-0.3 wt. % chloride and/or 0.1-0.3 wt. % fluoride. A person skilled in the art knows how to select the content of fluorides, which are highly volatile in the melt, in the batch so that the finished glass contains the aforesaid proportion.


The glass is preferably TiO2-free. Minor amounts of TiO2 may however enter the glass, for example through the raw material alumina. The TiO2 content is, however, limited to <100 ppm.


In order to vary the coefficient of thermal expansion α20/300, the glass may also contain further components, such as Li2O, BaO in amounts of at most 1%, which do not detrimentally affect the properties required for use.


Except for impurities, for example V2O5, the glass preferably consists of the components SiO2, B2O3, Al2O3, Na2O, K2O, CaO, optionally MgO, Fe2O3 and optionally TiO2 in the aforesaid amounts.


In a preferred embodiment, the sum of the amounts of the alkaline-earth metal oxides present in the glass is ≦3.9 mol %. This makes it easier to set α20/300 within the described limits of >5.3-5.8*10−6/K. A lower limit of >0.9 mol % is preferred for the sum of the alkaline-earth metal oxides present in the glass used according to the invention. This makes it easier to achieve a low melting temperature.


For this preferred embodiment, CaO+MgO≦3.9 mol % applies for the particularly preferably used glasses, which except for impurities contain only CaO and MgO as alkaline-earth metal oxides.


For glasses that contain only CaO as alkaline-earth metal oxide, the upper limit is specified by the maximum CaO content of 3.2 wt %.


In another preferred embodiment, the ratio of the amounts of the alkaline-earth metal oxides present in the glass (in mol %) to the sum of the amounts of the alkali metal oxides present (in mol %) is <0.55. This also makes it easier to set α20/300 in the desired range. Furthermore, the specified ratio has a particularly favourable effect on the tensile strength. A lower limit of >0.1 is preferred for this ratio.


For this preferred embodiment, (Na2O+K2O)/(CaO+MgO)<0.55 or (Na2O+K2O)/CaO<0.55 applies for the particularly preferably used glasses, which contain only Na2O and K2O as alkali metal oxides and which, except for impurities, contain only CaO and optionally MgO as alkaline-earth metal oxides. A lower limit of >0.1 is preferred for this ratio.


In another preferred embodiment, the ratio of a total amount of Al2O3 (in mol %) to the sum of the amounts of the alkali metal oxides (in mol %) in the glass used according to the invention is <0.6. In particular, this also makes it easier to set α20/300 in the desired range. A ratio of ≦0.55 is particularly preferred. A ratio <0.51 is more particularly preferred.


For this preferred embodiment, Al2O3/(Na2O+K2O)<0.6, particularly preferably ≦0.55, more particularly preferably <0.51 applies for the particularly preferably used glasses which contain only Na2O and K2O as alkali metal oxides.


In another preferred embodiment, the ratio of a total amount of B2O3 (in mol %) to the sum of the total amount of the B2O3 plus the sum of the amounts of the alkali metal oxides (in mol %) is <0.55. This lowers the melting temperature further. A ratio <0.5 is particularly preferred. It has a particularly favourable effect on the coefficient of thermal expansion.


For this preferred embodiment, B2O3/(B2O3+Na2O+K2O)<0.55 applies for the particularly preferably used glasses which contain only Na2O and K2O as alkali metal oxides. A ratio <0.5 is particularly preferred.


In another preferred embodiment, the ratio of SiO2/B2O3 (each in mol %) is >10.0. This leads to an improvement of the hydrolytic stability of the glass. A ratio of SiO2/B2O3 (each in mol %) of 13±0.5 is particularly preferred.


According to a preferred use, the metal of the glass-metal bonds is a metal material in group no. 1.3981 according to DIN 17745. This material has the following composition (in % by weight): 28-30, Ni; up to 0.05, C; 16-18, Co; and remainder Fe.


The glass may be fined with conventional fining agents, such as Sb2O3, As2O3, NaCl, BaCl, CaCl, MgCl, V2O5, Na2SO4, BaSO4, in conventional amounts, i.e. for example with additions of up to 0.5 wt. %. V2O5 is preferably avoided.







EXAMPLES

Three examples of glasses according to the invention (A) and two comparative examples of glasses (V) were melted from conventional raw materials.


For these exemplary embodiments A1-A3 and comparative glasses V1-V2, Tables I and III report the compositions in wt. % (Table I) and in mol % together with various sums, ratios and ratios of sums of the constituents (Table III). Table II shows the following important properties for the exemplary embodiments and comparative examples:

    • the coefficient of thermal expansion α20/300 [10−6/K]
    • the transformation temperature Tg [° C.]
    • the processing temperature VA [° C.]
    • the temperature at which the glass was melted, referred to here as the “melting temperature” [° C.]
    • the relative hydrolytic stability, measured according to ISO 719 and then normalized with the aid of V2
    • the relative tensile strength, calculated and then normalized with the aid of V2
    • the relative batch cost, normalized relative to V2
    • the solar transmission in the wavelength interval from 300 to 2500 nm [%]









TABLE I







Compositions (In Wt % Based On Oxide) Of Glasses According


To The Invention (A) And Comparative Glasses (V)













A1
A2
A3
V1
V2


















SiO2
74.5
74.5
75.6
75.5
74.0



Al2O3
6.5
6.4
6.4
6.4
6.5



Na2O
6.2
6.5
6.2
5.8
6.6



K2O
2.6
2.0
2.2
1.0
2.6



CaO
2.0
2.8
2.9
3.1
0.7



MgO

0.5
0.4
0.4




B2O3
7.9
7.0
6.0
7.5
9.4











All the glasses in table I contain 0.04 wt. % Fe2O3. All these glasses furthermore contain 0.04 wt. % BaO as impurities and 0.19 wt. % chloride and 0.06 wt. % fluoride as fining agents.









TABLE II







Selected Properties Of Glasses According To The Invention (A) And Comparative Glasses (V)













A1
A2
A3
V1
V2
















α20/300 [10−6/K]
   5.7
   5.7
   5.6
   5.04
   5.7


Tg [° C.]
558
570
574
578
565


VA [° C.]
1177 
1185 
1204 
1214 
1175 


“Melting temp.” [° C.]
1412 
1366 
1394 
1398 
1500 


Hydrolyt. stability
125
146
149
179
100



(relative to 100
(relative to 100
(relative to 100
(relative to 100
(normalized)



as standard)
as standard)
as standard)
as standard)


Tensile strength
  102.1
  103.3
  103.4
  106.2
100



(relative to 100
(relative to 100
(relative to 100
(relative to 100
(normalized)



as standard)
as standard)
as standard)
as standard)


Batch cost
 94
 88
 84
 90
100



(relative to 100
(relative to 100
(relative to 100
(relative to 100
(normalized)



as standard)
as standard)
as standard)
as standard)


Solar Transmission
>92
>92
>92
>92
>92


(300-2600 nm) [%]
















TABLE III







Compositions (In Mol % On Oxide) Of Glasses According


To The Invention (A) And Comparative Glasses (V) Plus


The Sums And Ratios Of Selected Components













A1
A2
A3
V1
V2
















SiO2
77.9
77.4
78.6
78.3
77.6


Al2O3
4
3.9
3.9
3.9
4


Na2O
6.3
6.6
6.2
5.8
6.7


K2O
1.7
1.3
1.5
0.7
1.7


CaO
2.2
3.1
3.2
3.4
0.8


MgO
0
0.8
0.6
0.6
0


B2O3
7.2
6.3
5.4
6.7
8.5


BaO
0.02
0.02
0.02
0.02
0.02


Cl
0.33
0.33
0.33
0.33
0.33


F
0.2
0.2
0.2
0.2
0.2


Fe2O3
0.02
0.02
0.02
0.02
0.02


Al2O3/Σ R2O
0.5
0.49
0.51
0.60
0.48


B2O3/(B2O3 + Σ R2O)
0.47
0.44
0.41
0.51
0.50


Σ RO/Σ R2O
0.2775
0.50
0.50
0.63
0.10


Σ RO
2.2
3.9
3.8
4.0
0.8


SiO2/B2O3
10.8
12.3
14.6
11.7
9.1










Comparative example V1 is unsuitable for the use according to the invention owing to its coefficient of expansion. Comparative example V2 has to be melted at a disadvantageously high melting temperature.


As the exemplary embodiments make clear, the glasses according to the invention have the following properties, which are advantageous in particular for their use according to the invention:

    • They have a thermal expansion α20/300 of between >5.3×10−6/K and 5.8×10−6/K, in preferred embodiments about 5.7×10−6/K, and are therefore matched to the expansion behavior of metals used in glass-metal bonds for tube collectors, in particular metal materials of no. 1.3981 according to DIN 17745
    • They have a transformation temperature of at most 580° C., in preferred embodiments at most 575° C. With these transformation temperatures, the collector or receiver tubes consisting of these glasses can be readily processed. Higher transformation temperatures would entail greater energy consumption for manufacturing the receivers.
    • They have a processing temperature VA of at most 1215° C., in preferred embodiments at most 1185° C. With these processing temperatures, the collector or receiver tubes consisting of these glasses can be readily processed. Higher processing temperatures would entail greater energy consumption for manufacturing the receivers.
    • The glasses have a very high hydrolytic stability, which is advantageous for processing the glasses and using the tubes.
    • They have a high tensile strength, which is important for processing and using the tubes.
    • The glasses have the desired high solar transmission.
    • Their total cost is relatively low. It is about 10% lower than that of the known glasses for the use according to the invention.
    • The glasses according to the invention can be melted at much lower temperatures, namely <1500° C., preferably <1400° C., compared with the known glasses for the use according to the invention. The energy consumption is therefore reduced by about 10%. Furthermore, the net output of the melting unit is increased.


With these properties, the glasses are straightforward and economical to produce. They can readily be processed to form glass tubes, even with sizeable diameters. They are outstandingly suitable for use as a glass tube in a tube collector having a glass-metal bond.


While the invention has been illustrated and described as embodied in a glass composition formulated for a glass-metal bond of a tube collector and glass-metal bond made with glass of that glass composition, it is not intended to be limited to the details shown, since various modifications and changes may be made without departing in any way from the spirit of the present invention.


Without further analysis, the foregoing will so fully reveal the gist of the present invention that others can, by applying current knowledge, readily adapt it for various applications without omitting features that, from the standpoint of prior art, fairly constitute essential characteristics of the generic or specific aspects of this invention.


What is claimed is new and is set forth in the following appended claims.

Claims
  • 1. A glass-metal bond in a tube collector of a solar energy collection apparatus, said glass-metal bond comprising a glass tube and a metal component bonded to the glass tube, wherein said glass tube has a glass composition comprising:
  • 2. The glass-metal bond according to claim 1, wherein said glass composition comprises:
  • 3. The glass-metal bond according to claim 1, wherein said glass composition comprises 0.1-0.3 wt. % chloride and/or 0.1-0.3 wt. % fluoride.
  • 4. The glass-metal bond according to claim 1, wherein, except for impurities, said glass composition consists of:
  • 5. The glass-metal bond according to claim 1, wherein said sum of said amounts of said alkaline-earth metal oxides in said glass composition is >0.9 mol % and ≦3.9 mol %.
  • 6. The glass-metal bond according to claim 1, wherein said ratio of said sum of said amounts of said alkaline-earth metal oxides, in mol %, to the said sum of said amounts of said alkali metal oxides, in mol %, is >0.1 and <0.55.
  • 7. The glass-metal bond according to claim 1, wherein a ratio of a total amount of Al2O3, in mol %, in said glass composition to said sum of said amounts of said alkali metal oxides, in mol %, is <0.6.
  • 8. The glass-metal bond according to claim 1, wherein a ratio of respective total amounts of Fe2+ and Fe3+ in the glass composition is from 0.03-0.1.
  • 9. The glass-metal bond according to claim 8, wherein said ratio of said respective total amounts of said Fe2 and said Fe3+ is from 0.045-0.055.
  • 10. The glass-metal bond according to claim 1, wherein said metal part consists of metal material no. 1.3981 according to DIN 17745.
  • 11. A glass having a glass composition comprising:
  • 12. The glass according to claim 11, wherein said glass composition comprises:
  • 13. The glass according to claim 11, wherein said glass composition comprises 0.1-0.3 wt. % chloride and/or 0.1-0.3 wt. % fluoride.
  • 14. The glass according to claim 11, wherein, except for impurities, said glass composition consists of:
  • 15. The glass according to claim 11, wherein said sum of said amounts of said alkaline-earth metal oxides in said glass composition is >0.9 mol % and ≦3.9 mol %.
  • 16. The glass according to claim 11, wherein said ratio of said sum of said amounts of said alkaline-earth metal oxides, in mol %, to the said sum of said amounts of said alkali metal oxides, in mol %, is >0.1 and <0.55.
  • 17. The glass according to claim 11, wherein a ratio of a total amount of Al2O3, in mol %, in said glass composition to said sum of said amounts of said alkali metal oxides, in mol %, is <0.6.
  • 18. The glass according to claim 11, wherein a ratio of respective total amounts of Fe2+ and Fe3+ in the glass composition is from 0.03-0.1.
  • 19. The glass according to claim 18, wherein said ratio of said respective total amounts of said Fe2+ and said Fe3+ is from 0.045-0.055.
Priority Claims (1)
Number Date Country Kind
10 2008 047 280 Sep 2008 DE national
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Number Date Country
44 30 710 May 1996 DE
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Related Publications (1)
Number Date Country
20100069221 A1 Mar 2010 US