Title of Invention

"AQUEOUS SOLUTIONS OF OPTICAL BRIGHTENERS"

Abstract The instant invention relates to storage stable aqueous solutions of stilbene optical brighteners with polyvinyl alcohols which can be directly used by the papermaker in that they may be diluted with water and/or be metered directly into a coating 5 composit ion, to provide coated papers of a particularly high whiteness.
Full Text AQUEOUS SOLUTIONS OF OPTICAL BRIGHTENERS
The instant invention relates to storage stable aqueous solutions of stilbene optical brighteners with polyvinyl alcohols which can be directly used by the papermaker.
It is well known that the whiteness and thereby the attractiveness of coated papers can be improved by the addition of optical brighteners to the coating slip. In order to satisfy the demand for coated papers of higher whiteness, there is a need for more efficient optical brighteners.
WO 96/00221 discloses tetrasulphonated stilbene brighteners derived from amino acids for use in paper, textiles and detergents. Polyvinyl alcohols are included in a list of additives which are said to boost the performance of brighteners when applied to the surface of paper.
WO 98/42685 discloses hexasulphonated stilbene brighteners made by using certain amino acids, disclaiming the compounds of WO 96/00221. Also described is a method for the fluorescent whitening of a paper surface by applying the brightener as part of a pigmented coating composition which also comprises polyvinyl alcohol as a water-soluble co-binder or protective colloid.
EP 1355004 describes the use of certain stilbene brighteners which are not derived from amino acids for brightening aqueous coating slips comprising at least one latex binder and at least one synthetic co-binder differing therefrom. Polyvinyl alcohols are cited as being preferred synthetic co-binders.
Japanese Kokai 62-106965 discloses certain hexasulphonated stilbene brighteners derived from amino acids. The brighteners are claimed to be very effective for the fluorescent whitening of paper, and may be applied to the paper surface as part of a sizing solution or a pigmented coating composition. Polyvinyl alcohol is mentioned as a possible component of the sizing solution.
Even though it is known from the prior art that polyvinyl alcohol, among other compounds, can boost the brightening performance, until now the papermaker, when wanting to use said alcohol, has had to add it separately to the coating slip. Therefore a need still exists to simplify the process of preparing brightened, coated papers.
It has now surprisingly been found that it is possible to produce storage stable solutions consisting essentially of a stilbene optical brightener and a polyvinyl alcohol which may be used directly by the papermaker, in that they may be diluted with water and/or be metered directly into a coating composition, to provide coated papers of a particularly high whiteness.
The invention thus provides aqueous optical brightener solutions consisting essentially of
(a) at least one optical brightener of formula (1)
(Formula Removed)
in which
M is hydrogen, an alkali metal atom, ammonium or a cation derived from an
amine, preferably hydrogen or sodium, most preferably sodium, n is 1 or 2, and X is a natural or unnatural amino acid from which a hydrogen atom of the
amino group has been removed;
(b) polyvinyl alcohol having a degree of hydrolysis greater than 75% and a
Brookfield viscosity of 2-40 mPa.s (4% w/w aqueous solution at 20°C); and
(c) water.
In optical brighteners for which n is 1, the SO3M group is preferably in the 4-position of the phenyl ring.
In optical brighteners for which n is 2, the SO3M groups are preferably in the 2,5-positions of the phenyl ring.
Examples of amino acids from which X may be derived are alanine, 2-aminobutyric acid, asparagine, aspartic acid, S-carboxymethylcysteine, cysteic acid, cysteine, glutamic acid, glutamine, glycine, iminodiacetic acid, isoleucine, leucine, methionine, N-methyltaurine, norleucine, norvaline, phenylalanine, 2-phenylglycine, pipecolinic acid, proline, sarcosine, serine, taurine, threonine, and valine. Where the amino acid contains a chiral centre, either optical isomer, or the racemic mixture, can be used.
Preferred amino acids are aspartic acid, glutamic acid and iminodiacetic acid.
The aqueous solutions may contain up to 10% by weight of salt, typically sodium chloride, formed as a by-product from the production of the optical brightener.
The aqueous solutions may also contain one or more antifreezes, biocides, complexing agents or other additives, as well as organic by-products formed during the preparation of the optical brightener.
The polyvinyl alcohol preferably has a degree of hydrolysis greater than or equal to 80% and a Brookfield viscosity of 2-20 mPa.s.
Preferably the weight ratio of polyvinyl alcohol to optical brightener lies in the range 0.01:1 to 1.5:1. More preferably, the ratio lies in the range 0.03:1 to 1:1.
The water content of the solution is suitably at least such that the solution is still stirrable and preferably easily pourable; in concentrated solutions the concentration of
the optical brightener is advantageously in the range 6 to 60%, preferably 10 to 50% by weight of the solution.
The pH of the aqueous solutions is preferably from neutral to clearly alkaline, in particular in the range pH 7 to pH 10. The pH may, if necessary, be adjusted by addition of M-corresponding bases, e.g. alkali metal hydroxides or carbonates, ammonia or amines.
The optical brightener solutions of the invention are storage-stable and may be used directly as such, in that they may be diluted with water and/or be metered directly into a coating composition. Thus a further object of the invention is the addition of the brightener solutions to coating compositions in order to obtain a coated and optically brightened paper.
Thus, the invention also provides a process for the production of coated paper that is optically brightened at least in the coating, wherein a coating composition as described above is coated onto paper after sheet formation.
The coating compositions are essentially aqueous compositions that contain at least one binder and a white pigment, in particular an opacifying white pigment, and may additionally contain further additives such as dispersing agents and defoamers.
Although it is possible to produce coating compositions that are free from white pigments, the best white substrates for printing are made using opaque coating compositions that contain 10-70% white pigment by weight. Such white pigments are generally inorganic pigments, e.g., aluminium silicates (kaolin, otherwise known as china clay), calcium carbonate (chalk), titanium dioxide, aluminium hydroxide, barium carbonate, barium sulphate, or calcium sulphate (gypsum).
The binders may be any of those commonly used in the paper industry for the production of coating compositions and may consist of a single binder or of a mixture of primary and secondary binders. The sole or primary binder is preferably a synthetic latex, typically a styrene-butadiene, vinyl acetate, styrene acrylic, vinyl acrylic or
ethylene vinyl acetate polymer. The secondary binder may be, e.g., starch, carboxymethylcellulose, casein, soy polymers, or polyvinyl alcohol.
The sole or primary binder is used in an amount typically in the range 5-25% by weight of white pigment. The secondary binder is used in an amount typically in the range 0.1-10% by weight of white pigment.
The optical brightener of formula (1) is used in an amount typically in the range 0.01-1% by weight of white pigment, preferably in the range 0.05-0.5% by weight of white pigment.
EXAMPLES
The following examples shall explain the instant invention in more detail. If not indicated otherwise, "%" and "parts" are by weight; viscosities are measured on a 4% aqueous solution at 20°C using a Brookfield viscometer.
PREPARATIVE EXAMPLE 1A
Optical brightener solution la is produced by stirring together
13.1 parts (O.Olmol) of an optical brightener of formula (4),
6.3 parts of a polyvinyl alcohol having a degree of hydrolysis of 98.5% and a
Brookfield viscosity of 2.75 mPa.s, and 80.6 parts of water
while heating to 90-95°C, until a clear solution is obtained that remains stable after
cooling to room temperature. The pH of the solution is adjusted to 9.0 with sodium
hydroxide.
(Figure Removed)
PREPARATIVE EXAMPLE IB
Optical brightener solution Ib is produced by stirring together
15.1 parts (O.Olmol) of an optical brightener of formula (5),
6.3 parts of a polyvinyl alcohol having a degree of hydrolysis of 98.5% and a
Brookfield viscosity of 2.75 mPa.s, and 78.6 parts of water
while heating to 90-95°C, until a clear solution is obtained that remains stable after
cooling to room temperature. The pH of the solution is adjusted to 9.0 with sodium
hydroxide.
(Figure Removed)
PREPARATIVE EXAMPLE 1C
Comparative Example (without polyvinyl alcohol)
Optical brightener solution Ic is produced by stirring together
15.1 parts (O.Olmol) of an optical brightener of formula (5), and 84.9 parts of water. The pH of the solution is adjusted to 9.0 with sodium hydroxide.
PREPARATIVE EXAMPLE ID
Comparative Example representing the State-of-the-art (EP 1355004)
Optical brightener solution Id is produced by stirring together
12.2 parts (O.Olmol) of an optical brightener of formula (6),
6.3 parts of a polyvinyl alcohol having a degree of hydrolysis of 98.5% and a
Brookfield viscosity of 2.75 mPa.s, and 81.5 parts of waterwhile heating to 90-95°C, until a clear solution is obtained that remains stable after
cooling to room temperature. The pH of the solution is adjusted to 9.0 with sodium
hydroxide.
(Figure Removed)
PREPARATIVE EXAMPLE 2A
Optical brightener solution 2a is produced by stirring together
13.1 parts (O.Olmol) of an optical brightener of formula (4),
6.3 parts of a polyvinyl alcohol having a degree of hydrolysis of 85% and a
Brookfield viscosity of 3.7 mPa.s, and 80.6 parts of water
while heating to 90-95°C, until a clear solution is obtained that remains stable after
cooling to room temperature. The pH of the solution is adjusted to 9.0 with sodium
hydroxide.
PREPARATIVE EXAMPLE 2B
Optical brightener solution 2b is produced by stirring together
15.1 parts (O.Olmol) of an optical brightener of formula (5),
6.3 parts of a polyvinyl alcohol having a degree of hydrolysis of 85% and a
Brookfield viscosity of 3.7 mPa.s, and 78.6 parts of water while heating to 90-95°C, until a clear solution is obtained that remains stable
after cooling to room temperature. The pH of the solution is adjusted to 9.0 with sodium
hydroxide.
PREPARATIVE EXAMPLE 2C
Comparative Example (without polyvinyl alcohol)
Optical brightener solution 2c is produced by stirring together
15.1 parts (O.Olmol) of an optical brightener of formula (5), and 84.9 parts of water. The pH of the solution is adjusted to 9.0 with sodium hydroxide.

PREPARATIVE EXAMPLE 2D
Comparative Example representing the State-of-the-art (EP 1355004)
Optical brightener solution 2d is produced by stirring together
12.2 parts (O.Olmol) of an optical brightener of formula (6),
6.3 parts of a polyvinyl alcohol having a degree of hydrolysis of 85% and a
Brookfield viscosity of 3.7 mPa.s, and 81.5 parts of water
while heating to 90-95°C, until a clear solution is obtained that remains stable after
cooling to room temperature. The pH of the solution is adjusted to 9.0 with sodium
hydroxide.
PREPARATIVE EXAMPLE 3A
Optical brightener solution 3 a is produced by stirring together
18.9 parts (0.0125mol) of an optical brightener of formula (5),
1.2 parts of a polyvinyl alcohol having a degree of hydrolysis of 85% and a
Brookfield viscosity of 3.7 mPa.s, and 79.9 parts of water
while heating to 90-95°C, until a clear solution is obtained that remains stable after
cooling to room temperature. The pH of the solution is adjusted to 9.0 with sodium
hydroxide.
PREPARATIVE EXAMPLE 3B
Comparative Example (without polvvinvl alcohol)
Optical brightener solution 3b is produced by stirring together
18.9 parts (0.0125mol) of an optical brightener of formula (5), and 81.1 parts of water. The pH of the solution is adjusted to 9.0 with sodium hydroxide.
APPLICATION EXAMPLE 1
A coating composition is prepared containing 500 parts chalk (commercially available under the trade name Hydrocarb 90 from OMYA), 500 parts clay (commercially available under the trade name Kaolin SPS from IMERYS), 470 parts water, 6 parts dispersing agent (a sodium salt of a polyacrylic acid commercially available under the trade name Polysalz S from BASF), 200 parts latex (an acrylic ester copolymer commercially available under the trade name Acronal S320D from BASF) and 50 parts of a 10% solution of carboxymethyl cellulose (commercially available under the trade name Finnfix 5.0 from Noviant) in water. The solids content is adjusted to 60% by the addition of water, and the pH is adjusted to 8-9 with sodium hydroxide.
Solutions la, 1b,1c and 1d, made as described in Preparative Examples 1 A, IB, 1C and 1D respectively, are added at a range of concentrations from 0.5 to 4.0% to the stirred coating composition. The brightened coating composition is then applied to a commercial 75gsm neutral-sized white paper base sheet using an automatic wire-wound bar applicator with a standard speed setting and a standard load on the bar. The coated paper is then dried for 5 minutes in a hot air flow. The dried paper is allowed to condition, then measured for CIE Whiteness on a calibrated Elrepho spectrophotometer.
TABLE 1

(Table Removed)
APPLICATION EXAMPLE 2
Application Example 1 is repeated using Solutions 2a, 2b, 2c and 2d, made as described in Preparative Examples 2A, 2B, 2C and 2D respectively.
TABLE 2

(Table Removed)
APPLICATION EXAMPLE 3
A coating composition is prepared containing 500 parts chalk (commercially available under the trade name Hydrocarb 90 from OMYA), 500 parts clay (commercially available under the trade name Kaolin SPS from IMERYS), 370 parts water, 6 parts dispersing agent (a sodium salt of a polyacrylic acid commercially available under the trade name Polysalz S from BASF), 200 parts latex (an acrylic ester copolymer commercially available under the trade name Acronal S320D from BASF) and 400 parts of a 20% solution of an anionic potato starch (Perfectamyl A4692 from AVEBE B.A.) in water. The solids content is adjusted to 60% by the addition of water, and the pH is adjusted to 8-9 with sodium hydroxide.
Solutions 3a and 3b, made as described in Preparative Examples 3A and 3B respectively, are added at a range of concentrations from 0.5 to 4.0% to the stirred coating composition. The brightened coating composition is then applied to a commercial 75gsm neutral-sized white paper base sheet using an automatic wire-wound bar applicator with a standard speed setting and a standard load on the bar. The coated
paper is then dried for 5 minutes in a hot air flow. The dried paper is allowed to condition, then measured for CIE Whiteness on a calibrated Elrepho spectrophotometer.
TABLE 3

(Table Removed)
The instant results clearly show the surprising superiority in whiteness of the instant solutions containing polyvinyl alcohol.






CLAIMS
1. Aqueous optical brightener solutions consisting essentially of (a) at least one optical brightener of formula (1)

(Formula Removed)
in which
M is hydrogen, an alkali metal atom, ammonium or a cation derived from
an amine, n is 1 or 2, and X is a natural or unnatural amino acid from which a hydrogen atom of
the amino group has been removed;
(b) polyvinyl alcohol having a degree of hydrolysis greater than 75% and a
Brookfield viscosity of 2-40 mPa.s; and
(c) water.
2. Solutions according to claim 1 wherein M is hydrogen or sodium, n is 1 or 2,
X is aspartic acid, glutamic acid or iminoacetic acid, and wherein the polyvinyl alcohol has a degree of hydrolysis of greater than or equal to 80% and a Brookfield viscosity of 2-20 mPa.s
3. Solutions according to claim 1 or 2 wherein the weight ratio of polyvinyl alcohol
to the optical brightener is from 0.01:1 to 1.5:1 and wherein the concentration of
the optical brightener is from 6 to 60% by weight.
4. Solutions according to claim 3 wherein the weight ratio of polyvinyl alcohol to
the optical brightener is from 0.03:1 to 1:1 and wherein the concentration of the
optical brightener is from 10 to 50% by weight.
5. Use of solutions according to any of the preceding claims for coating
compositions for paper.
6. Process for the production of coated paper wherein a coating compositon
containing a solution according to any of the preceeding claims is coated onto
paper after sheet formation.
7. Process according to claim 6 wherein the coating composition contains from 10 to
70 % by weight of one or more white pigments.
8. Process according to claim 6 or 7 wherein the coating composition contains a
primary binder based on synthetic latex selected from styrene-butadiene, vinyl
acetate, styrene acrylic, vinyl acrylic or ethylene vinyl acetate polymer or
additionally a secondary binder selected from starch, carboxymethylcellulose,
casein, soy polymers, or polyvinyl alcohol.
9. Process according to any of claims 6 to 8 wherein the primary binder is used in an
amount from 5 to 25% by weight of white pigment, wherein the secondary binder
is used in an amount from 0.1 to 10% by weight of white pigment and wherein the
optical brightener of formula (1) is used in an amount from 0.01 to 1% by weight
of white pigment, preferably from 0.05 to 0.5% by weight of white pigment.

Documents:

7651-delnp-2007-Abstract-(20-01-2014).pdf

7651-delnp-2007-abstract.pdf

7651-delnp-2007-Claims-(20-01-2014).pdf

7651-delnp-2007-claims.pdf

7651-delnp-2007-Correspondence Others-(15-10-2013).pdf

7651-delnp-2007-Correspondence Others-(20-01-2014).pdf

7651-delnp-2007-Correspondence Others-(20-06-2014).pdf

7651-delnp-2007-Correspondence Others-(29-10-2013).pdf

7651-delnp-2007-Correspondence-others-(14-10-2014).pdf

7651-delnp-2007-correspondence-others.pdf

7651-delnp-2007-description (complete).pdf

7651-delnp-2007-form-1.pdf

7651-delnp-2007-form-2.pdf

7651-delnp-2007-Form-3-(14-10-2014).pdf

7651-delnp-2007-Form-3-(15-10-2013).pdf

7651-delnp-2007-form-3.pdf

7651-delnp-2007-Form-5-(20-01-2014).pdf

7651-delnp-2007-form-5.pdf

7651-delnp-2007-GPA-(20-01-2014).pdf

7651-delnp-2007-pct-101.pdf

7651-delnp-2007-pct-105.pdf

7651-delnp-2007-pct-210.pdf

7651-delnp-2007-pct-237.pdf

7651-delnp-2007-pct-304.pdf

7651-delnp-2007-pct-306.pdf

7651-delnp-2007-Petition-137-(20-01-2014).pdf

7651-delnp-2007-Petition-138-(29-10-2013).pdf

Petition.pdf


Patent Number 265381
Indian Patent Application Number 7651/DELNP/2007
PG Journal Number 09/2015
Publication Date 27-Feb-2015
Grant Date 20-Feb-2015
Date of Filing 05-Oct-2007
Name of Patentee CLARIANT FINANCE (BVI) LIMITED
Applicant Address CITCO BUILDING, WICKHAMS CAY, P.O.BOX 662, ROAD TOWN, TORTOLA, VIRGIN ISLANDS, BRITISH
Inventors:
# Inventor's Name Inventor's Address
1 ANDREW CLIVE JACKSON 25 WALTON PARK, PANNAL, HARROGATE HG3 1EJ, GREAT BRITAIN
2 ALEC STEWART TINDAL FLAT 60, THE MIDDLEHAM, ASPECT 14, ELMWOOD LANE, LEEDS LS2 8WE, GREAT BRITAIN
3 MARIELA GAUTO FLAT 3, CAPEL HOUSE, CAPEL STREET, CALVERLEY, LEEDS LS28 5NU, GREAT BRITAIN
PCT International Classification Number D21H 21/30
PCT International Application Number PCT/EP2006/061329
PCT International Filing date 2006-04-05
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 05007691.8 2005-04-08 EPO