U.S. patent application number 10/747956 was filed with the patent office on 2004-08-05 for alkali metal fluorozincate and method for producing it.
This patent application is currently assigned to Solvay Fluor und Derivate GmbH. Invention is credited to Becker, Andreas, Frehse, Joachim, Seseke-Koyro, Ulrich.
Application Number | 20040151655 10/747956 |
Document ID | / |
Family ID | 7637261 |
Filed Date | 2004-08-05 |
United States Patent
Application |
20040151655 |
Kind Code |
A1 |
Seseke-Koyro, Ulrich ; et
al. |
August 5, 2004 |
Alkali metal fluorozincate and method for producing it
Abstract
Novel methods for producing alkali metal fluorozincates,
especially potassium fluorozincate. Products having defined
particle size ranges are obtained depending on the sequence of
introduction of the reactants alkali metal hydroxide, zinc oxide
and hydrogen fluoride. The resulting alkali metal fluorozincates
are particularly suitable for use as a fluxing agent or fluxing
agent additive during brazing of aluminum or aluminum alloys and
can be applied by wet or dry fluxing methods depending on the
particle size of the alkali metal fluorozincate particles.
Inventors: |
Seseke-Koyro, Ulrich;
(Isernhagen, DE) ; Becker, Andreas; (Lachendorf,
DE) ; Frehse, Joachim; (Hannover, DE) |
Correspondence
Address: |
CROWELL & MORING LLP
INTELLECTUAL PROPERTY GROUP
P.O. BOX 14300
WASHINGTON
DC
20044-4300
US
|
Assignee: |
Solvay Fluor und Derivate
GmbH
Hannover
DE
|
Family ID: |
7637261 |
Appl. No.: |
10/747956 |
Filed: |
December 31, 2003 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10747956 |
Dec 31, 2003 |
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10262612 |
Oct 2, 2002 |
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6743409 |
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10262612 |
Oct 2, 2002 |
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PCT/EP01/03509 |
Mar 28, 2001 |
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Current U.S.
Class: |
423/464 ;
148/26 |
Current CPC
Class: |
B23K 35/3605 20130101;
C01G 9/006 20130101 |
Class at
Publication: |
423/464 ;
148/026 |
International
Class: |
C01B 009/08 |
Foreign Application Data
Date |
Code |
Application Number |
Apr 3, 2000 |
DE |
100 16 257.6 |
Claims
What is claimed is:
1. A method for producing alkali metal fluorozincate from alkali
metal hydroxide, zinc oxide, and alkali metal fluoride or hydrogen
fluoride in aqueous phase, wherein: a) to produce fine alkali metal
fluorozincate, alkali metal hydroxide and zinc oxide are mixed into
a suspension and hydrogen fluoride is added, or b) to produce
medium fine alkali metal fluorozincate, hydrogen fluoride and zinc
oxide are mixed with one another and alkali metal hydroxide is
added, or c) to produce coarse alkali metal fluorozincate, hydrogen
fluoride and zinc oxide are mixed with one another and alkali metal
fluoride is added.
2. A method according to claim 1, for producing fine alkali metal
fluorozincates, wherein alkali metal hydroxide is mixed into a
suspension with zinc oxide in aqueous phase, and the suspension is
reacted with hydrogen fluoride to form fine alkali metal
fluorozincate.
3. A method according to claim 1, wherein the alkali metal
hydroxide is potassium hydroxide and potassium fluorozincate is
produced.
4. A method according to claim 1, wherein potassium hydroxide is
used in the form of as an aqueous potassium hydroxide solution.
5. A method according to claim 3, wherein the atomic ratio of K:Zn
is in the range from 1:1.+-.0.05, and the atomic ratio of (K+Zn):F
is in the range from 1:3.+-.0.05.
6. A method according to claim 1, further comprising isolating and
drying the alkali metal fluorozincate produced.
7. A method according to claim 2, wherein the suspension of alkali
metal hydroxide and zinc oxide is produced at a temperature in the
range from 15 to 85.degree. C., and the suspension subsequently is
reacted with hydrogen fluoride at a temperature up to 90.degree.
C.
8. A fine alkali metal fluorozincate produced by the method of
claim 1, and having a grain spectrum in which 50% of all particles
have a diameter <5 .mu.m.
9. An alkali metal fluorozincate according to claim 8, wherein
alkali metal is potassium.
10. A potassium fluorozincate according to claim 9, having a grain
spectrum in which 50% of all particles have a diameter <3.8
.mu.m.
11. A medium fine alkali metal fluorozincate produced by the method
of claim 1, and having a grain spectrum in which 50% of all
particles have a diameter <11 .mu.m.
12. A coarse alkali metal fluorozincate produced by the method of
claim 1, and having a grain spectrum in which 50% of all particles
have a diameter >11 .mu.m.
13. A method of fluxing an aluminum or aluminum alloy component for
brazing, said method comprising applying to said component a
fluxing agent comprising an alkali metal fluorozincate according
claim 8.
14. A method according to claim 13, wherein said fluxing agent is
applied by electrostatic dry fluxing.
15. A method of fluxing an aluminum or aluminum alloy component to
be brazed, said method comprising applying to said component a
fluxing agent comprising an alkali metal fluorozincate according to
claim 11.
16. A method of fluxing an aluminum or aluminum alloy component to
be brazed, said method comprising applying to said component a
fluxing agent comprising an alkali metal fluorozincate according to
claim 12.
17. A method according to claim 16, wherein said fluxing agent is
applied by wet fluxing from an aqueous or organic suspension.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of international patent
application no. PCT/EP01/03509, filed Mar. 28, 2001, designating
the United States of America and published in German as WO
01/74715, the entire disclosure of which is incorporated herein by
reference. Priority is claimed based on Federal Republic of Germany
patent application no. DE 100 16 257.6, filed Apr. 3, 2000.
BACKGROUND OF THE INVENTION
[0002] The present invention relates to a method for producing
alkali metal fluorozincate, to the resulting product, and to the
use thereof in brazing aluminum.
[0003] Alkali metal fluorozincates, such as cesium fluorozincate
and particularly potassium fluorozincate, may be used as fluxing
agents for brazing aluminum components and components made of
aluminum alloys. In this case, these compounds act not only as
fluxing agents, but rather they produce a coating of the surface,
in that zinc is deposited on the surface of the components. The
fluorozincates may also be used together with alkali
fluoroaluminates, for example potassium fluoroaluminate and/or
cesium fluoroaluminate. These compounds also act as fluxing agents
for brazing aluminum. German Published Application 199 13 111 A1
discloses these types of fluxing agents and their use. The
production of alkali metal fluorozincates according to this
published application is achieved by melting together alkali metal
fluoride and zinc fluoride, by reacting alkali metal fluoride and
zinc fluoride in aqueous phase, or by reacting zinc oxide with
adducts of hydrogen fluoride and alkali metal fluoride.
SUMMARY OF THE INVENTION
[0004] It is an object of the invention to provide a method for
producing alkali metal fluorozincates which is capable of producing
products having defined grain distribution ranges.
[0005] Another object of the invention is to provide an alkali
metal fluorozincate which is especially suited for use as a fluxing
agent or fluxing agent component.
[0006] These and other objects are achieved in accordance with the
present invention by providing a method for producing alkali metal
fluorozincate from alkali metal hydroxide, zinc oxide, and alkali
metal fluoride or hydrogen fluoride in aqueous phase, wherein:
[0007] a) to produce fine alkali metal fluorozincate, alkali metal
hydroxide and zinc oxide are mixed into a suspension and hydrogen
fluoride is added, or
[0008] b) to produce medium fine alkali metal fluorozincate,
hydrogen fluoride and zinc oxide are mixed with one another and
alkali metal hydroxide is added, or
[0009] c) to produce coarse alkali metal fluorozincate, hydrogen
fluoride and zinc oxide are mixed with one another and alkali metal
fluoride is added.
[0010] In accordance with a further aspect of the invention, the
objects are achieved by providing a fine alkali metal fluorozincate
produced by the method of claim 1, and having a grain spectrum in
which 50% of all particles have a diameter <5 .mu.m, or a medium
fine alkali metal fluorozincate produced by the method of claim 1,
and having a grain spectrum in which 50% of all particles have a
diameter <11 .mu.m, or a coarse alkali metal fluorozincate
produced by the method of claim 1, and having a grain spectrum in
which 50% of all particles have a diameter >11 .mu.m.
[0011] In accordance with yet another aspect of the invention, the
objects are achieved by providing a method of fluxing an aluminum
or aluminum alloy component for brazing, said method comprising
applying to said component a fluxing agent comprising an alkali
metal fluorozincate produced as described above.
[0012] The present invention is based on the recognition that
alkali metal fluorozincate having specific grain size properties
may be produced as a function of the type of starting compounds and
the sequence in which the starting reactants are brought into
contact with one another.
[0013] The method according to the present invention for producing
alkali metal fluorozincate from alkali metal hydroxide, zinc oxide,
and alkali metal fluoride or hydrogen fluoride in aqueous phase is
distinguished in that
[0014] a) to produce fine alkali metal fluorozincate, alkali metal
hydroxide and zinc oxide are mixed into a suspension, and hydrogen
fluoride is added, or
[0015] b) to produce medium fine alkali metal fluorozincate,
hydrogen fluoride and zinc oxide are mixed with one another, and
potassium hydroxide is added, or
[0016] c) to produce coarse alkali metal fluorozincate, zinc oxide
and hydrogen fluoride are mixed with one another, and alkali metal
fluoride is added.
[0017] Instead of zinc oxide, other zinc compounds, e.g., zinc
hydroxide, zinc carbonate, or zinc chloride, may be used. However,
zinc oxide is preferred.
[0018] In the context of the present invention, the term "fine"
refers to an alkali metal fluorozincate in which 50% of the
particles have a particle size smaller than 5 .mu.m and 90% of the
particles have a particle size of less than 9 .mu.m; the remaining
particles are then the same size or larger than the indicated
values. Fine alkali metal fluorozincate is preferably produced in
which 50% of all particles have a diameter of <3.8 .mu.m and 90%
of all particles have a diameter of <8 .mu.m. The size is
determined using laser diffraction.
[0019] Within the context of the present invention, the term
"medium fine" refers to a product in which 50% of the particles of
the material produced have a grain size of less than 11 .mu.m and
90% have a grain size of less than 27 .mu.m. The diameters of the
remaining particles are at or above the listed values. "Medium
fine" preferably means that 50% of all particles produced have a
grain size of less than 10 .mu.m and 90% of all particles have a
grain size of less than 26 .mu.m. The particle size analysis is
again carried out by laser diffraction.
[0020] In the context of the present invention, the term "coarse"
means that 50% of all particles have a grain size of less than 22
.mu.m and 90% have a grain size of less than 40 .mu.m. The term
"coarse" preferably means that 50% of all particles have a grain
size of less than 21 .mu.m and 90% have a grain size of less than
39 .mu.m. The diameters of the remaining particles correspond to
the recited dimensions or lie below them.
[0021] Alkali metal hydroxide, hydrogen fluoride, and alkali metal
fluoride advantageously are used in the form of an aqueous
solution. The preferred alkali metal is potassium.
[0022] In the first variant of the method according to the present
invention, fine alkali metal fluorozincate is formed. The fine
alkali metal fluorozincate preferably is then isolated and dried.
Surprisingly, the resulting product is finer than the product which
results according to the method described in German Published
Application 199 13 111. For example, alkali metal fluorozincate
having a grain spectrum in which 50% of all particles have a
diameter of <5 .mu.m (measured by laser diffraction) may be
produced in this way.
[0023] Preferably, the procedure starts with potassium hydroxide as
an alkali hydroxide and produces potassium fluorozincate. In this
case, the potassium hydroxide is preferably used in the form of an
aqueous potassium hydroxide solution. The concentration of KOH in
this potassium hydroxide solution is advantageously in the range
from 10 to 50 weight-percent. KZnF.sub.3 is particularly preferably
produced. For this purpose, potassium hydroxide, zinc oxide, and
hydrogen fluoride are preferably used in quantities such that the
atomic ratio of K:Zn is in the range from 1:1.+-.0.05 and the
atomic ratio of (K+Zn):F is in the range from 1:3.+-.0.05. The zinc
oxide may also be replaced by a zinc oxide precursor, for example,
ZnCO.sub.3 or ZnCl.sub.2.
[0024] A suspension is formed, which then reacts further with
hydrogen fluoride to obtain the desired alkali metal fluorozincate.
Preferably, a hydrofluoric acid solution is used containing 10 to
99 weight-percent HF, preferably 20 to 40 weight-percent HF.
[0025] The suspension of alkali metal hydroxide and zinc oxide is
preferably produced at a temperature in the range from 15 to
85.degree. C., particularly at ambient temperature (approximately
20.degree. C.). The resulting intermediate product is
advantageously reacted with hydrogen fluoride at a temperature in
the range from approximately 20.degree. C. to 90.degree. C.
[0026] In the second variant of the present invention, medium fine
alkali metal fluorozincate is produced. Hydrogen fluoride and
alkali hydroxide are preferably used as an aqueous solution. The
preferred concentrations correspond to those of the first variant.
Alkali preferably is represented by potassium. Hydrogen fluoride
and zinc oxide, which may be used in precursor form as zinc
carbonate, for example, are reacted at a temperature in the range
from 20.degree. C. (ambient temperature) to 95.degree. C. The
subsequent reaction with the hydroxide is preferably carried out at
a temperature in the range from 70.degree. C. to 90.degree. C.
[0027] For the third variant, in which coarse alkali metal
fluorozincate is produced, hydrogen fluoride is initially reacted
with zinc oxide, and then alkali metal fluoride is added. In this
case as well, alkali preferably is represented by potassium.
Hydrogen fluoride is preferably used in aqueous solution, the
preferred concentration being as in the first variant. The alkali
metal fluoride is also preferably used in aqueous solution. The
preferred alkali metal fluoride concentration lies in the range
from 25 to 40 weight-percent, particularly 28 to 32 weight-percent.
The temperature of the first reaction step is in the same range as
in variant 1 and variant 2. The addition of alkali metal fluoride
is then preferably carried out at a temperature of 70.degree. C. to
90.degree. C.
[0028] As noted above, the invention also relates to the fine,
medium fine, and/or coarse alkali metal fluorozincate, obtained
according to the variants of the method according to the present
invention, having the further parameters indicated above in regard
to the grain size. Potassium fluorozincate is preferred,
particularly potassium fluorozincate of the formula KZnF.sub.3. In
this case, the grain sizes of the fine product--in relation to 50%
of the particles, d.sub.X50--are in the range from 3 to 5 .mu.m,
those of the medium fine product are in the range from 6 to 11
.mu.m, and those of the coarse product are in the range from 12 to
25 .mu.m. Experiments have shown that it is possible to produce
potassium fluorozincate, for example, having an even finer grain
spectrum (e.g., 50% of the particles having a diameter of less than
3.3 .mu.m).
[0029] If a mixture of potassium hydroxide and rubidium, lithium,
or cesium hydroxide is used, corresponding mixed fluorozincates of
the type alkali.sub.1-xalkali'.sub.xZnF.sub.3 (x<1 and alkali
not equal to alkali') may be produced. These mixed fluorozincates
are also a subject of the present invention. In the case of mixed
fluorozincates, potassium-cesium fluorozincate (the ratio of
potassium to cesium being arbitrary) is preferred.
[0030] The fluorozincates according to the present invention are
particularly suitable for use as a fluxing agent for brazing
aluminum and aluminum alloys. They are then used in a known way,
for example, as disclosed in German Published Application 199 13
111. The fine product is particularly suitable for application
through wet fluxing, the coarse product for application by dry
fluxing. The medium fine product is well suited for both purposes.
Of course, mixtures having predetermined properties may also be
produced.
[0031] The fluorozincates of the invention are also suitable for
use as a solder fluxing agent additive for other fluxing agents,
particularly as a fluxing agent additive for potassium
fluoroaluminate and cesium fluoroaluminate.
[0032] The alkali metal fluorozincate according to the present
invention may, of course, also be mixed with alkali metal
fluorozincate produced in typical ways, in order to influence
properties such as suspensibility or fluidizability.
[0033] For example, the alkali metal fluorozincate of the invention
may be used mixed with solder metal, or with a precursor for a
solder metal, for example with 5-95 weight-percent, relative to the
total fluxing agent, of alkali metal fluorosilicate such as
potassium hexafluorosilicate, see European Patent Application 810
057 and German Published Application 196 36 897, or with 10 to 80
weight-percent of copper, zinc, or germanium, which form a eutectic
mixture with aluminum, see U.S. Pat. No. 5,190,596.
[0034] The alkali metal fluorozincate of the invention may also be
used in a mixture with alkali fluoroaluminates, for example, with
KAlF.sub.4 or K.sub.2AlF.sub.5, as is analogously described in
German Published Application 199 13 111, or with cesium
fluoroaluminate. The latter is advantageous for Al alloys having
larger proportions of Mg.
[0035] Further auxiliary agents may be included, for example, as
described in German Published Application 199 13 111, p. 3. For
example, binders or dispersing agents may be included.
[0036] The fluxing agent may be applied in a known way to the
components made of aluminum or aluminum alloys to be bonded. Dry
application on the basis of electrostatic spraying technology is
possible due to the good fluidizing properties of the fluxing
agent. Alternatively, the fluxing agent may be applied in the form
of aqueous and/or organic suspensions or as a paste to the
materials to be bonded. Aqueous or organic slurries advantageously
contain 15 to 75 weight-percent of the fluxing agent. Suspensions
of the fluxing agent in organic liquids, expediently the substances
typically used as organic solvents, such as alcohols, particularly
methanol, ethanol, propanol, or isopropanol, as well as polyols,
may also be used. Other organic liquids ("carriers") include
ethers, for example, diethylene glycol monobutyl ether, ketones
such as acetone, and esters of alcohols, diols, or polyols. An
example of a binder for application as a paste is ethyl cellulose.
Using film formers, typically polymers which are soluble in organic
solvents, e.g., acetone, fluxing agent may be applied, possibly
with brazing metal or solder precursors, onto the workpiece and
produce a strongly adhering film after evaporation of the solvent.
Suitable polymers include, for example, (meth)acrylates. During
brazing, the film former vaporizes.
[0037] During application, the brazing metal, if it is necessary,
may be contained in the fluxing agent (as an admixed powder), it
may already be applied as a plating on the components to be brazed,
or it may be applied in addition to the fluxing agent.
[0038] The brazing temperature is a function of the brazing
material used or the metal or material forming the brazing
material. Below a solder metal liquidization temperature of
450.degree. C., according to the definition, one refers to soft
soldering (="soldering"), above this, to hard soldering
(="brazing"). There are low melting solders, such as zinc-aluminum
solders, which may be used from 390.degree. C., or pure zinc
solder, which may be used from 420.degree. C. for soldering. Other
solders may be brazed at higher temperatures. Al--Si--[Cu] solders
may be used from [530.degree. C.] or 577.degree. C.,
respectively.
[0039] In general, a brazing temperature of 600.degree. C. is
sufficient. Preferably, soldering or brazing is performed from
390.degree. C. to 600.degree. C., particularly from 420 to
590.degree. C. Ambient pressure is used in this case. It is also
possible to braze, for example, in vacuum, with vaporization of the
fluxing agent, as described in Japanese Patent Application
03/099795, is also possible. Flame or furnace soldering may also be
carried out, particularly in inert atmosphere (e.g., N.sub.2
atmosphere).
EXAMPLE 1
Fine Product
[0040] Reaction: KOH+ZnO+3HF->KZnF.sub.3+2H.sub.2O
1 Batch: 1) 0.5 ml KOH solution 45.2% w/w 62.3 g ZnO (99.9 cm
Aldrich) 40.9 g completely desalinated water 30.6 ml (CD water) 2)
HF solution 49.6% w/w 60.6 g CD water 60.6 ml cooling CD water 33
ml
[0041] Procedure:
[0042] 62.3 g of the 45.2% KOH w/w was diluted with 30.6 ml of CD
water and subsequently 40.9 g of ZnO was added and slurried while
being stirred. An HF solution made of 60.6 g of the 49.6% HF
solution and 60.6 g of CD water was then introduced from a dropping
funnel within 90 seconds. The temperature rose from 24.6.degree. C.
to 85.9.degree. C. For cooling, 33 ml of CD water was added. The
mixture was then stirred for one hour at 80.degree. C., the
precipitate was filtered off and dried for four hours at
180.degree. C.
2 Yield: quantitative XRD = KZnF.sub.3 Grain size (laser
diffraction): X.sub.50 = 3.28 .mu.m X.sub.90 = 6.98 .mu.m
EXAMPLE 2
Medium Fine Product
[0043] The product was produced as described in Example 1 with the
exception that batch 1 was produced by reacting HF solution with
zinc oxide, and batch 2 was the KOH solution.
3 Grain size X.sub.50 = 9.47 .mu.m X.sub.90 = 25.75 .mu.m
EXAMPLE 3
Coarse Product
[0044] The produce was produced as described in Example 1 with the
exception that batch 1 was produced by reaction of HF solution with
zinc oxide, and batch 2 was a solution of KF in water.
4 Grain size X.sub.50 = 20.50 .mu.m Grain size X.sub.90 = 38.18
.mu.m
EXAMPLE 4
Use for Brazing
[0045] A triturate of 3 g of the substance from Example 1 with
isopropanol was applied to a 25.times.25 mm aluminum sheet, which
was plated with AlSi solder, and an aluminum angle was placed on
top. This assembly was thermally treated in a laboratory brazing
oven in accordance with the Nocolok.RTM. brazing process
conditions. The brazing of the assembly was 100%.
[0046] The foregoing description and examples have been set forth
merely to illustrate the invention and are not intended to be
limiting. Since modifications of the described embodiments
incorporating the spirit and substance of the invention may occur
to persons skilled in the art, the invention should be construed
broadly to include all variations within the scope of the appended
claims and equivalents thereof.
* * * * *