U.S. patent application number 13/342034 was filed with the patent office on 2012-04-26 for compound and method for producing the same.
Invention is credited to Chi-Fa Hsieh, Tai-Kang Liu, Jui-Ming Yeh.
Application Number | 20120101203 13/342034 |
Document ID | / |
Family ID | 42231390 |
Filed Date | 2012-04-26 |
United States Patent
Application |
20120101203 |
Kind Code |
A1 |
Hsieh; Chi-Fa ; et
al. |
April 26, 2012 |
COMPOUND AND METHOD FOR PRODUCING THE SAME
Abstract
The invention provides a compound and method of producing the
same. The method of the invention includes the following steps.
First of all, Polycaprolactone (PCL), dimethylol propionic acid
(DMPA), 4,4'-methylenebis (cyclohexyl isocyanate) (H12MDI), and
dibutyltin dilaurate (DBT) are mixed in a solvent in the first
place and a solution is formed. This solution is then mixed with
triethylamine (TEA) and triethylene tetramine (TETA). After that,
amino-terminated anionic waterborne polyurethane (WPU) is produced.
A sol-gel process is proceeded with a mixture of amino-terminated
anionic waterborne polyurethane, tetraethylorthosilicate (TEOS)
without any extra catalyst, and a compound, waterborne
polyurethane-silica nanocomposite materials, is eventually
produced.
Inventors: |
Hsieh; Chi-Fa; (Zhongli
City, TW) ; Yeh; Jui-Ming; (Zhongli City, TW)
; Liu; Tai-Kang; (Longtan Shiang, TW) |
Family ID: |
42231390 |
Appl. No.: |
13/342034 |
Filed: |
January 1, 2012 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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12330382 |
Dec 8, 2008 |
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13342034 |
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Current U.S.
Class: |
524/261 ;
524/591 |
Current CPC
Class: |
C08K 9/08 20130101; C08G
18/3228 20130101; C09D 175/04 20130101; C08G 18/758 20130101; C08G
18/4277 20130101; C08G 18/0823 20130101; C08G 18/6659 20130101 |
Class at
Publication: |
524/261 ;
524/591 |
International
Class: |
C08K 5/5415 20060101
C08K005/5415; C08L 75/04 20060101 C08L075/04 |
Claims
1. A compound comprising: waterborne polyurethane, wherein the
terminal of the waterborne polyurethane comprises an amino group;
and silicon dioxide mixed with the waterborne polyurethane.
2. The compound of claim 1, wherein the amino group is primary
amine.
3. The compound of claim 1, wherein the waterborne polyurethane is
formed by the following steps: mixing polycaprolactone, dimethylol
propionic acid, 4,4'-methylenebis (cyclohexyl isocyanate),
dibutyltin dilaurate, triethylamine, and triethylene tetramine to
form a solution; and filtering the solution in a pressure-reducing
environment to form another solution comprising waterborne
polyurethane.
4. The compound of claim 3, wherein the solution is mixed with
tetraethylorthorsilicate to form a mixing solution and a sol-gel
process is proceeded in the mixing solution, so as to produce the
compound in the mixing solution.
Description
BACKGROUND OF THE INVENTION
[0001] 1. Field of the Invention
[0002] The present invention relates to a compound and method for
producing the same, and more particularly, the compound is the
waterborne polyurethane-silica composite material. Additionally,
the method of the present invention produces the waterborne
polyurethane-silica composite material without any extra
catalyst.
[0003] 2. Description of the Prior Art
[0004] Recently, organic-inorganic mixing nanocomposite material is
a major topic both in the industry and in the academia. It is
because the organic-inorganic nanocomposite material has
flexibility, ductility, rigidity, and high thermal stability, so as
to broaden the applied scope.
[0005] The nanoinorganic of the organic-inorganic nanocomposite
material is produced by a sol-gel process of inorganic alkoxide
(M(OR).sub.n), for example, SiO.sub.2, TiO.sub.2, and ZnO. Since
1970, the inorganic alkoxide is proceeded a sol-gel process by an
in-situ approach to form nanopraticles in an organic polymer, so as
to form organic-inorganic nanocomposite material. A sol-gel process
is to add acid or alkaline catalysts into an inorganic alkoxide
which is proceeding a hydrolytic reaction to form an inorganic
hydroxide (M(OH).sub.n). The chemical equation is as followed:
M(OR).sub.n+nH.sub.2O.fwdarw.M(OH).sub.n+nROH
[0006] Wherein M=Na, Ba, Cu, Al, Si, Ti, Ge, V, W, etc., and
R=CH.sub.3, C.sub.2H.sub.5, C.sub.3H.sub.7, C.sub.4H.sub.9-
M(OH).sub.n, in particular, comprises a functional group and thus
it can proceed a polymerization reaction to form O-M-O-M
three-dimensional network.
[0007] Additionally, polyurethane has both flexibility and
rigidity. It is low in cost, easy to manufacture, and various in
design. Thus it is widely applied to coating, building, and
electronic sealing. However, polyurethane is low in thermal
stability and high in hygroscopicity. On the primes of keeping the
features of the polyurethane, introducing inorganic to raise the
heat resistance and the water repellency of polyurethane composite
material becomes a popular study topic in related scopes.
[0008] According to the reference of producing polyurethane
composite material, polyurethane is classified into non-waterborne
polyurethane and waterborne polyurethane. The methods apply (A) for
producing non-waterborne polyurethane composite material classified
as (1) directly introducing silicon dioxide particles (e.g.
Min-U-Sil, colloidal silica, or fumed silica); and (2) silicon
dioxide formed by a sol-gel process with acid catalysts (e.g.
hydrochloric acid, acetic acid) or alkaline catalysts (e.g.
ammonia). Additionally, the methods apply (B) for producing
waterborne polyurethane composite material classified as (1)
directly introducing silicon dioxide particles (e.g. fumed silica);
and (2) silicon dioxide formed by a sol-gel process with acid
catalysts (e.g. hydrochloric acid). Moreover, we cannot find any
disclosure about sol-gel process with basic catalysts. As mentioned
above, if the method of directly introducing silicon dioxide
particles is not adopted, the polyurethane composite material is
produced with catalysts only.
SUMMARY OF THE INVENTION
[0009] Accordingly, an aspect of the present invention is to
provide a method for producing a compound. The compound is a
polyurethane composite material and the method of the present
invention produces the compound without any extra catalysts.
[0010] According to an embodiment of the invention, the method
comprises the following steps:
[0011] First of all, polycaprolactone (PCL), dimethylol propionic
acid (DMPA), 4, 4'-methylenebis (cyclohexyl isocyanate) (H12MDI),
and dibutyltin dilaurate (DBT) are mixed in a solvent to form the
first solution. Subsequently, the first solution is mixed with a
triethylamine (TEA) solution to form a second solution and the
second solution is mixed with deionized water to form a second
aqueous solution. The second aqueous solution is mixed with
triethylene tetramine (TETA) solution to form a third solution and
the third solution is filtered in a pressure-reducing environment
to obtain a waterborne polyurethane (WPU) solution. Particularly,
the terminal of the waterborne polyurethane comprises an amino
group.
[0012] Furthermore, the waterborne polyurethane solution is mixed
with tetraethylorthosilicate (TEOS) to form a fourth solution.
Finally, part of the fourth solution is coated on a carrier and the
solution on the carrier is heated, so as to produce the compound
with thin film type.
[0013] Another aspect of the present invention is to provide a
compound which is polyurethane composite material produced without
any extra catalyst.
[0014] According to one embodiment of the invention, the compound
comprises waterborne polyurethane and silicon dioxide. The terminal
of the waterborne polyurethane comprises an amino group which is
primary amine or other proper amino group. Silicon dioxide is mixed
with the waterborne polyurethane.
[0015] The objective of the present invention will no doubt become
obvious to those of ordinary skills in the art after reading the
following detailed description of the preferred embodiment, which
is illustrated in the various figures and drawings.
BRIEF DESCRIPTION OF THE APPENDED DRAWINGS
[0016] FIG. 1 illustrates a producing flow chart according to one
embodiment of the present invention.
[0017] FIG. 2 illustrates FTIR spectrums of PCL, DMPA, H12MDI, TETA
and WPU according to the present invention.
[0018] FIG. 3 illustrates .sup.29Si NMR spectrum of waterborne
polyurethane-silica nanocomposite material according to the present
invention.
[0019] FIG. 4 illustrates TEM image of waterborne
polyurethane-silica nanocomposite material of 20000 times according
to the present invention.
[0020] FIG. 5 illustrates contact angle testing result of
waterborne polyurethane-silica nanocomposite material according to
the present invention.
[0021] FIG. 6 illustrates the tension intensity of waterborne
polyurethane-silica nanocomposite material according to the present
invention.
[0022] FIG. 7 illustrates thermogravimetric analysis of waterborne
polyurethane-silica nanocomposite material according to the present
invention.
DETAILED DESCRIPTION OF THE INVENTION
[0023] The present invention is to provide a compound and method
for producing the same. The compound is a polyurethane composite
material and the method for producing the compound without any
extra catalyst. Embodiments of the present invention are disclosed
as followed.
[0024] Please refer to FIG. 1. FIG. 1 illustrates a flow chart
according to one embodiment of the present invention.
[0025] As shown in FIG. 1, in one embodiment, the method comprises
the following steps:
[0026] In step S110, PCL, DMPA, H12MDI, and DBT are mixed in a
solvent to form the first solution. Subsequently, in step S112, the
first solution is mixed with a TEA solution to form a second
solution. In step S114, the second solution is mixed with deionized
water to form a second aqueous solution. In step S116, the second
aqueous solution is mixed with TETA solution to form a third
solution. In step S118, the third solution is filtered in a
pressure-reducing environment to obtain a waterborne polyurethane
solution. The terminal of the waterborne polyurethane comprises an
amino group. In step S120, the waterborne polyurethane solution is
stirred rapidly and TEOS is added into the waterborne polyurethane
solution simultaneously by an simultaneously by an in-situ approach
to form the fourth solution. What is remarkable is the addition of
TEOS brings a sol-gel process, so as to produce the compound of the
present invention in the fourth solution. Finally, in step S122,
part of the fourth solution is coated on a carrier and the solution
on the carrier is heated, so as to form the compound with thin film
type.
[0027] The following detailed description describes the environment
of the present method. What should be marked is the following
procedures, materials, parameters and data are examples of the
present invention, but not limited to it.
[0028] First of all, a 500 ml PCL is set in a five-necked flask
equipped with a proper temperature control apparatus and a
pressure-reducing apparatus. PCL with magnetic stirring is degassed
in a pressure-reducing environment at 110.degree. C. for 30 minutes
and cools down to room temperature (30.degree. C.) under
pressure-reducing station. H12MDI, DMPA, DBT, and some solvent are
mixed to form a first solution which is proceeded a polymerization
reaction at 60.degree. C. for four hours. In practical application,
the composition of the solvent can be acetone.
[0029] After the first solution cools down to room temperature, the
first solution and TEA solution are mixed to form a second solution
wherein the TEA solution is formed by TEA mixed with the first
solvent and the composition of the first solvent is substantially
the same as the solvent. The second solution is stirred at
30.degree. C. for one hour and the second solution is mixed with
deionized water to form a second aqueous water. The second aqueous
water is mixed with TETA solution to form a third solution wherein
the TETA is mixed with the second solvent to form the TETA solution
and the composition of the second solvent is substantially the same
as the solvent. The third solution is stirred at 60.degree. C. for
one hour. After the third solution cools down to room temperature,
the third solution is filtered in a pressure-reducing environment
to get a waterborne polyurethane solution. The waterborne
polyurethane is determined by a moisture titrator and the
waterborne polyurethane occupies 26.5 wt %.
[0030] In one embodiment, the terminal of the waterborne
polyurethane comprises an amino group. In practical application,
the amino group can be prime amine or other proper amino group.
Additionally, the weight ratio of PCL:DMPA:H12MDI:TEA:TETA is
94.3:31.3:5.9:4.5:4.2, but not limited to this.
[0031] Additionally, the characteristic peak of PCL, DMPA, H12MDI,
TETA and waterborne polyurethane (WPU) are determined by FTIR. The
determining result is as follows. The C.dbd.O characteristic peak
of PCL exists at 1722 cm.sup.-1; the C--O and O--H characteristic
peak of DMPA exists at 1683 cm.sup.-1 and 3359 cm.sup.-1
respectively; and the N.dbd.C characteristic peak of H12MDI exists
at 2262 cm.sup.-1. After polymerization reaction to form WPU, the
N.dbd.C (2262 cm.sup.-1) and O-H characteristic peaks (3359
cm.sup.-1) disappear. The primary amine --NH.sub.2 exists at 3223
cm.sup.-1 and 3319 cm.sup.-1 that can prove the production is
amino-terminated anionic waterborne polyurethane.
[0032] Furthermore, the WPU solution with TEOS is proceeded as a
sol-gel process. First, pour some WPU solution into a beaker and
stir the WPU solution rapidly. TEOS is added into the WPU solution
simultaneously by an in-situ approach to form the fourth solution.
The fourth solution is stirred at room temperature for one hour to
proceed as a sol-gel process to obtain a composite solution. Part
of composite solution is coated on a carrier and the carrier is set
in a temperature-controllable non-convection baking oven. The
temperature raising process is shown in table 1. A compound with
thin film type on the carrier is obtained. As shown in table 1, the
compound with thin film type is formed at 55.degree. C., 75.degree.
C., 100.degree. C., and 120.degree. C.
TABLE-US-00001 TABLE 1 Process Temperature Time Temperature raised
Room temp.~55.degree. C. 16 hrs Holding temperature 55.degree. C. 5
hrs Temperature raised 55.degree. C.~75.degree. C. 10 hrs Holding
temperature 75.degree. C. 3 hrs Temperature raised 75.degree.
C.~100.degree. C. 5 hrs Holding temperature 100.degree. C. 3 hrs
Temperature raised 100.degree. C.~120.degree. C. 5 hrs Holding
temperature 120.degree. C. 3 hrs
[0033] In one embodiment, the compound produced by the method
mentioned comprising waterborne polyurethane and silicon dioxide
mixed with the waterborne polyurethane wherein the terminal of the
waterborne polyurethane comprises an amino group which can be
primary amine or other proper amino group.
[0034] Waterborne polyurethane-silica nanocomposite material formed
by an in-situ approach raises the heat resistance and the water
repellency of polyurethane. The rigidity, heat resistance, and the
water repellency are rising with the using weight of TEOS.
[0035] In practical application, the content of silicon dioxide may
change the characters of the compound of the present invention.
Table 2 lists four compounds of the invention and weight of TEOS
used. Sample a (SWPU) is waterborne polyurethane without silicon
dioxide; Sample b (SWPU5) is a waterborne polyurethane-silica
nanocomposite material with 5 wt % silicon dioxide (formed by
adding 2.42 g TEOS); Sample c (SWPU10) is a waterborne
polyurethane-silica nanocomposite material with 10 wt % silicon
dioxide (formed by adding 5.10 g TEOS); and Sample d (SWPU15) is a
waterborne polyurethane-silica nanocomposite material with 15 wt %
silicon dioxide (formed by adding 8.15 g TEOS).
TABLE-US-00002 TABLE 2 Sample Weight of WPU Used Weight of TEOS
Used a (SWPU) 50 g 0 g b (SWPU5) 50 g 2.42 g c (SWPU10) 50 g 5.10 g
d (SWPU15) 50 g 8.15 g
[0036] In the following, different samples by (1) contact angle,
(2) mechanical property, and (3) thermal property will be
analyzed.
[0037] First, sample d (SWPU15) is determined by .sup.29Si NMR to
obtain a silicon spectrum as shown in FIG. 3. FIG. 3 illustrates
the character peaks of silicon chemical shift at -108.72 ppm,
-98.14 ppm, and -93 ppm. The three character peaks correspond to
Q.sup.4, Q.sup.3, and Q.sup.2 constructions respectively. Q.sup.4,
Q.sup.3, and Q.sup.2 constructions are shown in the top right-hand
corner of FIG. 3. The character peak of Q.sup.4 is clear that can
prove the TEOS is proceeded as a sol-gel process to produce silicon
dioxide.
[0038] Additionally, FIG. 4 illustrates the TEM image of sample d
(SWPU15) of 20000 times. The dark particles are silicon dioxide and
the white parts are waterborne polyurethane base materials. The
length of dark particles are approximately 30.about.40 nm and
disturb in the waterborne polyurethane materials uniformly. It
shows that TEOS is proceeded as a sol-gel process to produce
silicon dioxide. The conclusion is the same as above.
[0039] (1) Contact Angle Testing
[0040] FIG. 5 illustrates the data of contact angles on the sample
surface determined by a contact angle meter. As shown in FIG. 5,
the contact angle of sample a (SWPU), without TEOS, is
67.2.degree.. Samples with TEOS, for example, sample b (SWPU5, 5 wt
% of silicon dioxide), the contact angle)(70.6.degree.) raises 5%,
compared with sample a, WPU with silicon dioxide can raise the
degree of contact angle. Raising the using weight of TEOS of
waterborne polyurethane, for example, sample c (SWPU10, 10 wt % of
silicon dioxide), the determined contact angle compared with sample
a raises 13% and sample d (SWPU15, 15 wt % of silicon dioxide), the
determined contact angle (78.4).degree. compared with sample a
raises 17%. As shown in FIG. 5, the contact angle of waterborne
polyurethane composite material raises with the using weight of the
TEOS (it can produce silicon dioxide).
[0041] (2) Mechanical Property
[0042] Determining the mechanical property by DMA, the strain speed
is set 1 N/min and the thickness of the sample is 150 .mu.m.
Determine the stress and strain of the samples at room temperature.
FIG. 6 illustrates the testing result of mechanical property of
samples with different content of silicon dioxide. Sample a (SWPU,
waterborne polyurethane without silicon dioxide), sample b (SWPU5,
waterborne polyurethane-silica composite material with 5 wt %
silicon dioxide), sample c (SWPU10, waterborne polyurethane-silica
composite material with 10 wt % silicon dioxide), and sample d
(SWPU15, waterborne polyurethane-silica composite material with 15
wt % silicon dioxide) are represented as (a), (b), (c), and (d)
respectively in FIG. 6. As shown in FIG. 6, take a sample, the
magnitude of strain is 100% and the magnitude of stress is 1.5 MPa.
A waterborne polyurethane base material with little TEOS, for
example, sample b (SWPU5), the magnitude of strain is 100% and the
magnitude of stress is 1.75 MPa compared with sample a, the
magnitude of stress raised by 19%. With the same magnitude of
stress, the magnitude of strain is 2.05 MPa for sample c (SWPU10);
and the magnitude of strain is 2.10 MP for sample d (SWPU15)
compared with the sample a, the magnitude of stress raising 35%.
The mechanical intensity rises with the weight of TEOS used.
[0043] (3) Thermal Property
[0044] The thermal stability of sample a, b, c and d are tested by
TGA at temperature 40.about.800.degree. C. The speed of raising
temperature is 10.degree. C./min and N.sub.2 gas is flown during
testing. The result is shown in FIG. 7. (a), (b), (c), and (d)
represent sample a (SWPU), sample b (SWPU5), sample c (SWPU10), and
sample d (SWPU15), respectively. The upper half of FIG. 7
illustrates the relationship between thermal weight losing and
temperature, and the lower half of FIG. 7 illustrates the
relationship between first order differentiation of thermal weight
losing and temperature. Table 3 lists the date of thermal
dissolution temperature. From the curve of first order
differentiation, every sample has three dissolution stages. The
first dissolution temperature is approximately 40.about.300.degree.
C. wherein thermal weight decreases lightly and the dissolution
temperature rises with the content of silicon dioxide. In the
stage, thermal weight changes 6.about.9 wt % and it may be due to
the remainder water or molecules decomposing and the polymer which
is aqueous dispersion polymer. The aqueous dispersion polymer
waterborne polyurethane comprises 26.5 wt % waterborne
polyurethane. After the TEOS is added to the solution, the content
of compound is increased and the content of solvent is decreased.
As shown in table 3, the thermal remainder weight is bigger than
waterborne polyurethane without silicon dioxide. The temperature of
the second dissolution stage is approximately 400.about.500.degree.
C. The soft chain of waterborne polyurethane-silica decomposes
mainly.
[0045] The relationship between thermal remainder weight and
temperature shows the compound with TEOS with higher thermal
resistance than waterborne polyurethane without silicon
dioxide.
TABLE-US-00003 TABLE 3 Thermal remainder weight and temperature
First dissolution stage, Second dissolution Third dissolution
40~300.degree. C. stage, 300~400.degree. C. stage, 400~500.degree.
C. Thermal Thermal Thermal remainder remainder remainder
weight.sup.a weight.sup.a weight.sup.a Sample wt % .degree. C.
T.sub.max.sup.b, .degree. C. wt % .degree. C. T.sub.max.sup.b,
.degree. C. wt % .degree. C. Sample a (SWPU) 91.5 282 321 26.3 380
409 0.2 465 Sample b (SWPU5) 92.8 286 359 32.5 393 418 2.0 492
Sample c (SWPU10) 93.9 288 374 32.0 404 423 4.2 494 Sample d
(SWPU15) 93.2 290 383 47.8 396 424 6.1 494 .sup.athermal remainder
weight at the temperature .sup.btemperature of the maximum
dissolution speed (T.sub.max)
[0046] To sum up, the present invention is to provide a method for
producing a compound. The compound is a polyurethane composite
material and the method of the present invention produces the
compound without any extra catalyst. Polyurethane has the
advantages of both being organic and inorganic. It is flexible,
ductile, rigid, and high in thermal stability, so as to widen the
applied scopes.
[0047] Although the present invention has been illustrated and
described with reference to the preferred embodiment thereof, it
should be understood that it is in no way limited to the details of
such an embodiment, but is capable of numerous modifications within
the scope of the appended claims.
* * * * *