U.S. patent application number 12/529442 was filed with the patent office on 2009-12-31 for use in a hydraulic binder composition of a dry-ground calcium carbonate with a copolymer of (meth) acrylic acid and an alkoxy or hydroxy polyalkyleneglycol group.
This patent application is currently assigned to COATEX S.A.S.. Invention is credited to Olivier Guerret, Yves Kensicher, Jacques Mongoin, Jean-Marc Suau.
Application Number | 20090326101 12/529442 |
Document ID | / |
Family ID | 38896638 |
Filed Date | 2009-12-31 |
United States Patent
Application |
20090326101 |
Kind Code |
A1 |
Suau; Jean-Marc ; et
al. |
December 31, 2009 |
USE IN A HYDRAULIC BINDER COMPOSITION OF A DRY-GROUND CALCIUM
CARBONATE WITH A COPOLYMER OF (METH) ACRYLIC ACID AND AN ALKOXY OR
HYDROXY POLYALKYLENEGLYCOL GROUP
Abstract
The invention resides in the use in a composition with a
hydraulic binder base, of a calcium carbonate characterised in that
it is obtained by dry-grinding, firstly, and in that it is
dry-ground in the presence of a grinding aid agent which is a
copolymer of (meth)acrylic acid with a monomer containing an alcoxy
or hydroxy polyalkyleneglycol group, secondly. The invention also
concerns the compositions with a hydraulic binder base thus
obtained.
Inventors: |
Suau; Jean-Marc; (Lucenay,
FR) ; Mongoin; Jacques; (Quincieux, FR) ;
Kensicher; Yves; (Theize, FR) ; Guerret; Olivier;
(La Tour De Salvagny, FR) |
Correspondence
Address: |
OBLON, SPIVAK, MCCLELLAND MAIER & NEUSTADT, L.L.P.
1940 DUKE STREET
ALEXANDRIA
VA
22314
US
|
Assignee: |
COATEX S.A.S.
Genay
FR
|
Family ID: |
38896638 |
Appl. No.: |
12/529442 |
Filed: |
February 26, 2008 |
PCT Filed: |
February 26, 2008 |
PCT NO: |
PCT/IB2008/000610 |
371 Date: |
September 8, 2009 |
Current U.S.
Class: |
524/3 ;
524/5 |
Current CPC
Class: |
C01P 2004/61 20130101;
C04B 40/0039 20130101; C04B 2103/52 20130101; C04B 28/02 20130101;
C04B 40/0039 20130101; C04B 28/02 20130101; C01P 2004/62 20130101;
C04B 24/2647 20130101; C09C 1/021 20130101; C04B 24/2647 20130101;
C04B 14/28 20130101; C04B 14/28 20130101 |
Class at
Publication: |
524/3 ;
524/5 |
International
Class: |
C04B 24/24 20060101
C04B024/24; C04B 24/26 20060101 C04B024/26 |
Foreign Application Data
Date |
Code |
Application Number |
Mar 5, 2007 |
FR |
07/01593 |
Claims
1. A dry-ground calcium carbonate for use in a hydraulic binder
composition, wherein said carbonate is dry-ground in the presence
of a copolymer as a grinding aid agent, and said copolymer
comprises: a) at least one anionic monomer chosen from among
acrylic acid, methacrylic acid and their blends, b) at least one
non-ionic monomer, of formula (I): ##STR00003## where: m, n, p and
q are integers such that: m, n, p.ltoreq.150, q.gtoreq.1, and
5.ltoreq.(m+n+p)q.ltoreq.150, R.sub.1 represents hydrogen or a
methyl or ethyl radical, R.sub.2 represents hydrogen or a methyl or
ethyl radical, R represents a radical containing an unsaturated
polymerisable function selected from the group of vinylics, the
group of acrylic, methacrylic, and maleic esters, the group of
unsaturated acrylurethane, methacrylurethane, .alpha.-.alpha.'
dimethyl-isopropenyl-benzylurethane, and allylurethane, the group
of allylic or vinylic ethers, whether or not substituted, the group
of ethylenically unsaturated amides and imides, and the group
constituted by acrylamide and methacrylamide, and R' represents
hydrogen or a hydrocarbonated radical with 1 to 40 carbon atoms, or
a blend of several monomers of formula (I), (c) and optionally at
least one other monomer selected from among (meth)acrylic
anhydride, (meth)acrylamide, the (meth)acrylic esters, with 1 to 20
carbon atoms in their ester radical, the methyl or ethyl
methacrylates, the hydroxylated methacrylates, the aromatic vinylic
monomers, the organophosphate monomers, and their blends.
2. The dry-ground calcium carbonate according to claim 1, wherein
said copolymer comprises, expressed as a percentage by weight of
the monomers and the sum of the percentages by weight of all the
monomers equals 100%: a) 0.5% to 50% of at least one anionic
monomer selected from acrylic acid, methacrylic acid and their
blends, b) 50% to 99.5% of at least one non-ionic monomer, of
formula (I): ##STR00004## where: m, n, p and q are integers such
that: m, n, p.ltoreq.150, q.gtoreq.1, and
5.ltoreq.(m+n+p)q.ltoreq.150, R.sub.1 represents hydrogen or a
methyl or ethyl radical, R.sub.2 represents hydrogen or a methyl or
ethyl radical, R represents a radical containing an unsaturated
polymerisable function selected from the group of vinylics, the
group of acrylic, methacrylic, and maleic esters, the group of
unsaturated acrylurethane, methacrylurethane, .alpha.-.alpha.'
dimethyl-isopropenyl-benzylurethane, and allylurethane, the group
of allylic or vinylic ethers, whether or not substituted, the group
of ethylenically unsaturated amides and imides, and the group
constituted by acrylamide and methacrylamide, and R' represents
hydrogen or a hydrocarbonated radical with 1 to 40 carbon atoms, or
a blend of several monomers of formula (I), and (c) 0% to 50% of at
least one other monomer selected from among (meth)acrylic
anhydride, (meth)acrylamide, the (meth)acrylic esters with 1 to 20
carbon atoms in their ester radical, the methyl or ethyl
methacrylates, the hydroxylated methacrylates, the aromatic vinylic
monomers, the organophosphate monomers, and their blends.
3. The dry-ground calcium carbonate according to claim 1, wherein
said copolymer is in the acidic form and optionally distilled, and
is partially or totally neutralised by one or more neutralisation
agents having a monovalent or polyvalent cation, where the said
agents are selected from ammonia, calcium and magnesium hydroxides
and/or oxides, sodium, potassium and lithium hydroxides, and the
aliphatic and/or cyclic primary, secondary or tertiary amines.
4. The dry-ground calcium carbonate according to claim 1, wherein
said copolymer is obtained by processes of radical polymerisation
in solution, in a direct or reverse emulsion, in suspension or
precipitation in solvents, in the presence of catalytic systems and
chain transfer agents, or by processes of controlled radical
polymerisation by nitroxide mediated polymerisation (NMP) or by
cobaloximes, by atom transfer radical polymerisation (ATRP), and by
controlled radical polymerisation by sulphurated derivatives,
chosen from carbamates, dithioesters or trithiocarbonates (RAFT) or
xanthates.
5. The dry-ground calcium carbonate according to claim 3, wherein
said copolymer may be, before or after the total or partial
neutralisation reaction, treated and separated into several phases,
according to static or dynamic processes by one or more polar
solvents belonging to the group consisting of water, methanol,
ethanol, propanol, isopropanol, the butanols, acetone,
tetrahydrofuran and their blends.
6. The dry-ground calcium carbonate according to claim 1, wherein
0.05% to 5% by dry weight of the said copolymer relative to the dry
weight of calcium carbonate is used during a dry grinding of the
said carbonate.
7. The dry-ground calcium carbonate according to claim 1, wherein
the hydraulic binder is a cement, a concrete or a mortar.
8. A hydraulic binder composition comprising the dry-ground calcium
carbonate according to claim 1.
Description
[0001] The present invention concerns the field of compositions
with hydraulic binder bases, containing at least one mineral matter
which is a calcium carbonate obtained by dry grinding.
[0002] Grinding using a dry process (as opposed to in an aqueous
medium) of calcium carbonate is described in the documents "Beitrag
zur Aufklarung der Wirkungsweise von Mahlhilfsmitteln" ("Freiberger
Forschungshefte" VEB Deutscher Verlag fur Grundstoffindustrie,
Leipzig, Germany (1975)). and "Calcium Carbonate" (Birkhauser
Verlag, 2001).
[0003] This grinding, which leads to a reduction in the size of the
individual particles of calcium carbonate by mechanical action, is
assisted by grinding agents which can be classified into the
following 3 categories.
[0004] The first comprises the weak acids (formic, acetic, lactic,
adipic as mentioned in document FR 2 863 914, or stearic as
indicated in document EP 0 510 890), and their salts (sodium lignin
sulfonate, sodium acetate, etc.). The second includes the weak
bases, and notably the amines (see document GB 2 179 268). The
third, and the most commonly used, since it is the most effective,
includes the glycol-based alcohols, including notably diethylene
glycol illustrated in documents WO 2002/081 573 and US 2003/019
399.
[0005] Although they are still the most effective, the latter lead
to calcium carbonates with a high quantity of volatile organic
compounds (VOCs). For this reason, finding an alternative solution
to these glycol-based grinding aid agents which is at least as
effective as them in terms of the final application would
constitute a major contribution to the state of the technique.
[0006] With this regard, a first object of the invention consists
in the use, in a composition with a hydraulic binder base, of a
calcium carbonate characterised in that the said carbonate is
dry-ground in the presence of a grinding aid agent, firstly, and in
that the grinding aid agent is, secondly, a copolymer, consisting:
[0007] a) of at least one anionic monomer chosen from among acrylic
acid, methacrylic acid and their blends, [0008] b) and of at least
one non-ionic monomer, of formula (I):
[0008] ##STR00001## [0009] where: [0010] m, n, p and q are integers
such that: m, n, p.ltoreq.150, q.gtoreq.1, and 5.ltoreq.(m+n+p)q
.ltoreq.150, and preferentially 15.ltoreq.(m+n+p)q.ltoreq.120,
[0011] R.sub.1 represents hydrogen or the methyl or ethyl radical,
[0012] R.sub.2 represents hydrogen or the methyl or ethyl radical,
[0013] R represents a radical containing an unsaturated
polymerisable function, preferentially belonging to the group of
vinylics, or to the group of acrylic, methacrylic, maleic esters,
or to the group of unsaturated urethanes such as acrylurethane,
methacrylurethane, .alpha.-.alpha.'
dimethyl-isopropenyl-benzylurethane, allylurethane, or to the group
of allylic or vinylic ethers, whether or not substituted, or again
to the group of ethylenically unsaturated amides or imides, or
again to the group constituted by acrylamide and methacrylamide,
[0014] R' represents hydrogen or a hydrocarbonated radical with 1
to 40 carbon atoms, preferentially 1 to 4 carbon atoms, where R' is
very preferentially the methyl radical, [0015] or a blend of
several monomers of formula (I), [0016] c) and possibly of at least
one other monomer chosen from among (meth)acrylic anhydride,
(meth)acrylamide, or from among the (meth)acrylic esters, such as
preferentially the acrylates and methacrylates with 1 to 20 carbon
atoms in their ester radical, such as very preferentially the
methyl, ethyl, isopropyl, n-propyl, isobutyl, n-butyl, ter-butyl or
2-ethylhexyl acrylates, the methyl or ethyl methacrylates, the
hydroxylated methacrylates such as the hydroxyethyl and
hydroxypropyl methacrylates, or from among the aromatic vinylic
monomers such as preferentially styrene, .alpha.-methylstyrene,
styrene sulfonate, or acrylamido-2-methyl-2-propane-sulfonic acid,
or from among the organophosphate monomers, such as preferentially
the acrylate and methacrylate phosphates of ethylene glycol, or the
acrylate and methacrylate phosphates of oxyethylene and/or
oxypropylene glycol, and their blends.
[0017] This grinding aid agent may be designated using the
expression of a copolymer of methacrylic acid with a monomer
containing an alcoxy or hydroxy polyalkyleneglycol group.
[0018] The examples of the present Application show that, in
comparison with a calcium carbonate which is dry ground with a
diethylene glycol, a calcium carbonate according to the invention
enables a composition to be obtained with a hydraulic binder base
such as a mortar with a much higher degree of spreading.
[0019] This use is also characterised in that the said copolymer
consists, expressed as a percentage by weight of the monomers (the
sum of the percentages by weight of all the monomers equals 100%):
[0020] a) 0.5% to 50%, preferentially 1% to 25%, and very
preferentially 5% to 20%, of at least one anionic monomer chosen
from among acrylic acid, methacrylic acid and their blends, [0021]
b) 50% to 99.5%, preferentially 75% to 99%, and very preferentially
80% to 95%, of at least one non-ionic monomer, of formula (I):
[0021] ##STR00002## [0022] where: [0023] m, n, p and q are integers
such that: m, n, p.ltoreq.150, q.gtoreq.1, and 5.ltoreq.(m+n+p)q
.ltoreq.150, and preferentially 15.ltoreq.(m+n+p)q.ltoreq.120,
[0024] R.sub.1 represents hydrogen or the methyl or ethyl radical,
[0025] R.sub.2 represents hydrogen or the methyl or ethyl radical,
[0026] R represents a radical containing an unsaturated
polymerisable function, preferentially belonging to the group of
vinylics, or to the group of acrylic, methacrylic, maleic esters,
or to the group of unsaturated urethanes such as acrylurethane,
methacrylurethane, .alpha.-.alpha.'
dimethyl-isopropenyl-benzylurethane, allylurethane, or to the group
of allylic or vinylic ethers, whether or not substituted, or again
to the group of ethylenically unsaturated amides or imides, or
again to the group constituted by acrylamide and methacrylamide,
[0027] R' represents hydrogen or a hydrocarbonated radical with 1
to 40 carbon atoms, preferentially 1 to 4 carbon atoms, where R' is
very preferentially the methyl radical, [0028] or a blend of
several monomers of formula (I), [0029] c) 0% to 50% of at least
one other monomer chosen from among (meth)acrylic anhydride,
(meth)acrylamide, or from among the (meth)acrylic esters, such as
preferentially the acrylates and methacrylates with 1 to 20 carbon
atoms in their ester radical, such as very preferentially the
methyl, ethyl, isopropyl, n-propyl, isobutyl, n-butyl, ter-butyl or
2-ethylhexyl acrylates, the methyl or ethyl methacrylates, the
hydroxylated methacrylates such as the hydroxyethyl and
hydroxypropyl methacrylates, or from among the aromatic vinylic
monomers such as preferentially styrene, .alpha.-methylstyrene,
styrene sulfonate, or acrylamido-2-methyl-2-propane-sulfonic acid,
or from among the organophosphate monomers, such as preferentially
the acrylate and methacrylate phosphates of ethylene glycol, or the
acrylate and methacrylate phosphates of oxyethylene and/or
oxypropylene glycol, and their blends.
[0030] This use is also characterised in that the said copolymer is
obtained in the acidic form and possibly distilled, and is possibly
partially or totally neutralised by one or more neutralisation
agents having a monovalent or polyvalent cation, where the said
agents are chosen preferentially from among ammonia or from among
calcium, magnesium hydroxides and/or oxides, or from among sodium,
potassium or lithium hydroxides, or from among the aliphatic and/or
cyclic primary, secondary or tertiary amines, such as
preferentially stearylamine, the ethanolamines (mono-, di- and
triethanolamine), mono- and diethylamine, cyclohexylamine,
methylcyclohexylamine, amino methyl propanol, morpholine, and
preferentially in that the neutralisation agent is chosen from
among triethanolamine and sodium hydroxide.
[0031] This use is also characterised in that the said copolymer is
obtained by processes of radical polymerisation in solution, in a
direct or reverse emulsion, in suspension or precipitation in
solvents, in the presence of catalytic systems and chain transfer
agents, or again by processes of controlled radical polymerisation,
and preferentially by nitroxide mediated polymerisation (NMP) or by
cobaloximes, by atom transfer radical polymerisation (ATRP), by
controlled radical polymerisation by sulphurated derivatives,
chosen from among carbamates, dithioesters or trithiocarbonates
(RAFT) or xanthates.
[0032] This use is also characterised in that the said copolymer
may possibly, before or after the total or partial neutralisation
reaction, be treated and separated into several phases, according
to static or dynamic processes known to the skilled man in the art,
by one or more polar solvents belonging preferentially to the group
constituted by water, methanol, ethanol, propanol, isopropanol, the
butanols, acetone and tetrahydrofuran or their blends.
[0033] One of the phases then corresponds to the polymer used
according to the invention.
[0034] This use is also characterised in that 0.05% to 5%,
preferentially 0.1% to 3%, and very preferentially 0.1% to 1%, by
dry weight of the said copolymer relative to the dry weight of
calcium carbonate is used during the dry grinding of the said
carbonate.
[0035] This use is also characterised in that the composition with
a hydraulic binder is a cement, a concrete or a mortar.
[0036] A second purpose of the invention consists of the
compositions with a hydraulic binder base obtained by the use of
dry-ground calcium carbonate according to the invention.
EXAMPLES
[0037] In these examples, all the grinding operations are
undertaken according to a method well known to the skilled man in
the art (document FR 2 901 491 describes such a method). We shall
confine ourselves here to indicating the final granulometry of the
particles of calcium carbonate obtained after grinding (the skilled
man in the art in reality knows how to modify the parameters of the
process with a view to obtaining such a granulometry; however, one
may also refer to the above-mentioned document).
[0038] In each of the tests n.sup.o 1 to 4, a mortar is produced by
blending whilst stirring, according to the basic knowledge of the
skilled man in the art, a standard sand (EN 196-1), cement (CEM I
42.5 PM ES), tap water and a calcium carbonate ground according to
the prior art or according to the invention (the proportions are
given in table 1).
[0039] This preparation is used to fill an Abrams mini-cone
(minimum weight: 4 kg, upper diameter: 50 mm, lower diameter: 100
mm, height: 150 mm). The cone is positioned on a PVC plate dampened
using a sponge.
[0040] Filling lasts 2 minutes, and the contents of the cone are
settled by regularly "pricking" 25 times the preparation inside the
cone using a metal rod.
[0041] The cone is then raised when it is filled; its contents are
spread on the PVC plate. After 30 seconds the spreading is
determined by measuring the length in mm of two perpendicular
diameters of the round cake obtained, and by taking the average of
the two.
Test No. 1
[0042] This test illustrates the prior art and uses a calcium
carbonate obtained by dry grinding in the presence of 3000 ppm
(relative to the dry weight of calcium carbonate) of a grinding
agent of the prior art, which is diethylene glycol.
[0043] After grinding a calcium carbonate is obtained, 73.8% and
48.5% by weight of the particles of which have an average diameter
lower respectively than 2 .mu.m and 1 .mu.m (as measured using a
Sedigraph.TM. 5100).
Test No. 2
[0044] This test illustrates the prior art and uses a calcium
carbonate obtained by dry grinding in the presence of 3000 ppm
(relative to the dry weight of calcium carbonate) of a grinding
agent of the invention which is a polymer consisting, by weight
percentage, 81.5% of methoxy polyethylene glycol methacrylate of
molecular weight 2000, 4.9% of methacrylic acid, and 13.6% of
acrylic acid.
[0045] After grinding a calcium carbonate is obtained, 74.5% and
44.1% by weight of the particles of which have an average diameter
lower respectively than 2 .mu.m and 1 .mu.m (as measured using a
Sedigraph.TM. 5100).
Test No. 3
[0046] This test illustrates the prior art and uses a calcium
carbonate obtained by dry grinding in the presence of 1400 ppm
(relative to the dry weight of calcium carbonate) of a grinding
agent of the prior art, which is diethylene glycol.
[0047] After grinding a calcium carbonate is obtained, 47.1% and
30.0% by weight of the particles of which have an average diameter
lower respectively than 2 .mu.m and 1 .mu.m (as measured using a
Sedigraph.TM. 5100).
Test No. 4
[0048] This test illustrates the prior art and uses a calcium
carbonate obtained by dry grinding in the presence of 1400 ppm
(relative to the dry weight of calcium carbonate) of a grinding
agent of the invention which is a polymer consisting, by weight
percentage, 81.5% of methoxy polyethylene glycol methacrylate of
molecular weight 2000, 4.9% of methacrylic acid, and 13.6% of
acrylic acid.
[0049] After grinding a calcium carbonate is obtained, 45.4% and
28.0% by weight of the particles of which have an average diameter
lower respectively than 2 .mu.m and 1 .mu.m (as measured using a
Sedigraph.TM. 5100).
[0050] The polymer used in tests n.sup.o 2 and 4 is obtained by
polymerisation techniques well known to the skilled man in the
art.
[0051] In a first beaker the following are introduced at ambient
temperature and whilst stirring: 259.02 of methoxy polyethylene
glycol methacrylate of molecular weight equal to 2000 g/mol, a
solution containing 15.36 g of methacrylic acid and 274.39 g of
water, a solution containing 69.86 g of untreated water and 50.25 g
of acrylic acid
[0052] In a second beaker the following are introduced at ambient
temperature and whilst stirring: 2.38 g of thiolactic acid (of
98.5% mass purity) and 52.14 g of water.
[0053] In a third beaker the following are introduced at ambient
temperature and whilst stirring: 2.84 g of ammonium persulphate
(NH.sub.4).sub.2S.sub.2O.sub.8 and 51.90 g of water.
[0054] In a fourth beaker the following are introduced at ambient
temperature and whilst stirring: 0.56 g of ammonium persulphate
(NH.sub.4).sub.2S.sub.2O.sub.8 and 10.87 g of water.
[0055] In a single-casing cylindrical reactor, surmounted by a
refrigerating column, by an anchor stirring system and 3 inlets,
351.39 g of water and 295.61 g of isopropanol are introduced. The
reactive medium is heated whilst stirring (230 rpm) to
84.+-.2.degree. C. The contents of the first 3 beakers are
introduced into the reactive medium in 2 hours. The introduction
nozzles are then rinsed with 20.84 g of water (this water goes
directly into the reactive medium). The solution of the 4.sup.th
beaker is then added to the reactive medium, and the blend is fired
for 1 hour at 84.+-.2.degree. C. (at 230 rpm). At the end of the
reaction the device is rinsed with 52.13 g of water. The
temperature is then raised and 604.78 g is distilled. The
temperature is brought down to between 50 and 60.degree. C., and
69.34 g of sodium hydroxide at 50% mass in water is added to the
reactive medium. Finally the medium is diluted with 20.85 g of
water. It is cooled again before obtaining the polymer of the
invention.
[0056] The compositions of each mortar and the spreading values are
given in table 1.
TABLE-US-00001 TABLE 1 Test n.sup.o 1 2 3 4 Prior Art/ PA IN PA IN
Invention Sand 1767 1767 1767 1767 Cement 500 500 500 500 Water
234.85 234.85 234.85 234.85 Dry-ground CaCO3 150.15 150.15 150.15
150.15 Spreading (mm) 130 150 125 155
[0057] By comparing tests the 2 by 2 (1 to 2, and 3 to 4), it is
observed that the spreading of the mortars in the context of the
invention is much higher than for mortars formulated with calcium
carbonates of the prior art.
* * * * *