Title of Invention

TITANIUM DIOXIDE BASED COLOUR CONCENTRATE FOR POLYESTER MATERIALS

Abstract The invention is directed to a titanium dioxide based colour concentrate, suitable for colouring polyester materials, said concentrate comprising, based on the weight of the concentrate, more than 50 % of titanium dioxide, up to 20 % of at least one wax selected from the group of glycerol monostearate, hydrogenated castor oil and polyethoxylated glycols, and up to 30 % of at least one polyester.
Full Text TITANIUM DIOXIDE BASED COLOUR CONCENTRATE FOR POLYESTER MATERIALS
The invention is in the field of polyester materials, more in
particular in the field of colour concentrates for polyesters in the production of
packaging, such as bottles, for storing products that are sensitive to visible or
UV light.
The effects of light on milk and other dairy products sold in grocery
stores can adversely affect the product if it is not carefully packaged and
handled. Various strategies can be employed to minimize or eliminate the
photo oxidation in milk, which can result from the effects of light. The use of
properly formulated pigmented containers can significantly reduce milk
oxidation and vitamin depletion, however some potential problems exist with
pigments. Loss of nutrients in milk can to a large extent be prevented by
controlling store lighting, setting proper storage temperatures and using
closed storage cases.
Today, almost all milk is purchased in retail outlets such as
supermarkets and convenience stores. The density polyethylene (HDPE) bottle
is still widely used as package for milk as consumers like its ease of handling,
resealability and visible fill level. Initially, HDPE replaced glass bottles, but
since 1971 its growth has come largely at the expense of paper cartons.
Nowadays packaging materials like pouches are also used but especially
polyethylene terephthalate (PET) bottles are finding themselves more and
more in the centre of attention. Technical difficulties related to the protection
of dairy products/milk have up to now prevented the application of PET
packaging in this area.
Attempts have been made to modify the bottles to minimize fight
transmission. These include using ultraviolet (UV) light absorbers, as well as
incorporating various pigments into the plastic. Glass allows the highest light
transmission through the visible spectrum. Adding a UV absorber to the
natural bottle provides excellent protection in the ultraviolet light range below
380 nanometers, but gives little benefit in the visible, critical blue-violet visible
range of 400-550 nanometers.
Prior art multilayer bottles (PET with TiO2/black layer (PET)/PET
with TIO2) does not permit light transmittance, however, the black layer
shines through the bottle (really grey appearance) and the multilayer is more
expensive and processing is more difficult. The same applies for a multilayer
with a red layer (most red absorbs up to 550 nm) as the red layer shines
through, resulting in a reddish, pinkish appearance.
Incorporating white pigment (titanium dioxide, TiO2) into the
material significantly reduces, but does not completely eliminate, light
transmission in the harmful blue-violet region. A paper carton is not fully
opaque. It also allows some light transmission in the critical visible area.
However, by incorporating high levels of TiO2 in the polyester, i.e. amounts of
4 wt.% or over, it has become possible to obtain an opaque material having a
degree of transmission that is low enough to store UHT treated dairy products
for a sufficiently long period of time. Typically, this type of milk-products has a
shelf-life of about 3 months outside the refrigerator. In WO 2005/102865 such
a packaging material is described.
As indicated, the bottles of described in WO 2005/102865 provide a
reasonably good opacity and shielding of the contents thereof. However, there
is still need for improvement. Further, the processing properties of the
material is not very good, as it is relatively sensitive to delamination after
blow-moulding. This means that in the walls of the packaging delamination
occurs, with the result of decreased barrier properties and failure (breaking) of
the package, especially under pressure.
The cause of this phenomenon is uncertain, but it has now been
found that by the use of a specific titanium dioxide based colour concentrate,
these problems can be overcome. Further it has been found that the
transmission (or light blocking) properties of the material are improved in case
certain specific combinations of components are used.
In a first embodiment the invention is accordingly directed to a
titanium dioxide based colour concentrate, suitable for coloring polyester
materials, said concentrate comprising, based on the weight of the concentrate,
more than 50 % of titanium dioxide, up to 20 % of at least one wax selected
from the group of glycerol monostearate, hydrogenated castor oil and
polyethoxylated glycols, and up to 30 % of at least one polyester, such as
polyethylene-terephthalate.
The invention resides in the combined use of titanium dioxide, a
specific wax and polyester in the concentrate. Using a concentrate based on
these components in colouring the blow-moulded bottles or other biaxially
stretched packaging materials, results in a product possessing a good
resistance against delamination (even though the material has a high content
of titanium dioxide), while at the same time having a good transmission
profile, i.e. being opaque for visible and UV light, thereby providing a
packaging that enables a long shelf life for dairy products. It is to be noted that
other additive systems, such as those described in US patent 6,649,083, do not
provide the superior properties obtained by the present combination of
compounds, as is shown in the comparative examples
The first component of the concentrate is titanium dioxide. This can
be present in various crystal forms, rutile and anatase being the most
important. The amount of titanium dioxide is more than 50 wt.%, preferably at
least 60 wt.%. The upper limit is not very critical, but for practical purposes an
amount of at most 75 wt.% is preferred.
The second component is a wax, which is preferably present in an
amount of 1 to 10 wt.%. This wax is selected from the group of glycerol
monostearate, hydrogenated castor oil and polyethoxylated glycols.
Generally it is preferred that the wax has the following properties:
- is solid at 20°C and has a consistency, at that temperature, which can vary
from soft and plastic, to brittle and hard;
- if solid, then coarse to fine crystalline, transparent to opaque, but not glassy;
- melts without decomposition above 40°C;
- has a relatively low viscosity at a temperature which is somewhat above its
melting point;
- varies considerably in consistency and solubility by changing the
temperature;
- can be polished by rubbing under a light pressure.
In case a poly-ethoxylated glycol is used, this is preferably poly
ethylene glycol. Also combinations of waxes can be used in the present
invention.
A further component of the material of the present invention is at
least one polyester, optionally a combination of two or more polyesters. The
amounts thereof are up to 30 wt.%, preferably at least 5 wt.%.
The suitable polyester is a condensation product of a dibasic acid
and a glycol. Typically, the dibasic acid comprises an aromatic dibasic acid, or
ester or anhydride thereof, such as isophthalic acid, terephthalic acid,
naphthalene-l,4-dicarboxylic acid, naphthalene-2,6,-dicarboxylic acid, phthalic
acid, phthalic anhydride, tetrahydrophthalic anhydride, trimellitic anhydride,
diphenoxyethane-4,4,-dicarboxylic acid, diphenyl-4,4'-dicarboxylic acid, and
mixtures thereof. The dibasic acid also can be an aliphatic dibasic acid or
anhydride, such as adipic acid, sebacic acid, decane-l,10-dicarboxylic acid,
fumaric acid, succinic anhydride, succinic acid, cyclohexanediacetic acid,
glutaric acid, azeleic acid, and mixtures thereof. Other aromatic and aliphatic
dibasic acids known to persons skilled in the art also can be used. Preferably,
the dibasic acid comprises an aromatic dibasic acid, optionally further
comprising up to about 20%, by weight of the dibasic acid component, of an
aliphatic dibasic acid.
The glycol, or diol, component of the polyester comprises ethylene
glycol, propylene glycol, butane-l,4-diol, diethylene glycol, a polyethylene
glycol, a polypropylene glycol, neopentyl glycol, a polytetramethylene glycol,
1,6-hexylene glycol, pentane-l,5-diol, 3-methylpentanediol-(2,4), 2-
methylpentanediol-(l,4), 2,2,4-trimethylpentanediol-(l,3), 2-ethylhexanediol-
(1,3), 2,2-diethylpropanediol-(l,3), hexanediol-(l,3), 1,4-di-
(hydroxyethoxy)benzene, 2,2-bis-(4-hydroxycyclohexyl)propane, 2,4-dihydroxy-
1,1,3,3-tetramethylcyclobutane, 2,2-bis-(3-hydroxyethoxyphenyl)propane, 2,2-
bis-(4-hydroxypropoxyphenyl)propane, 1,4-dihydroxymethylcyclohexane, and
mixtures thereof. Additional glycols known to persons skilled in the art also
can be used as the glycol component of the diluent polyester.
In particular, the polyester preferably comprises PET ,e.g. but not
limiting, virgin bottle grade PET or postconsumer PET (PC-PET)), cyclohexane
dimethanol/PET copolymer (PETG), polyethylene naphthalate (PEN),
polybutylene terephthalate (PBT), and mixtures thereof. Suitable polyesters
also can include polymer linkages, side chains, and end groups different from
the formal precursors of the simple polyesters previously specified.
Suitable polyesters for use in the present invention typically have an
intrinsic viscosity of about 0.2 to about 1.2, and more preferably about 0.2 to
about 0.6 (for a 60/40 blend of phenol/tetrachloroethane solvent). For PET, an
intrinsic viscosity value of 0.6 corresponds approximately to a viscosity
average molecular weight of 36,000, and an intrinsic viscosity value of 1.2
corresponds approximately to a viscosity average molecular weight of 103,000.
The polyester optionally can include additives that do not adversely
affect the preblend, or preforms or containers prepared therefrom. The
optional additives include, but are not limited to, stabilizers, e.g., antioxidants
or ultraviolet light screening agents, extrusion aids, drying agents, fillers,
anticlogging agents, crystallization aids, impact modifiers, additives designed
to make the polymer more degradable or combustible, dyes, other pigments,
and mixtures thereof. The optional additives are present in the polyester in an
amount of 0% to about 2%, by weight of the polyester, individually, and 0% to
about 10%, by weight of the polyester, in total. The dyes and other pigments
may be used to provide a specific colour to the final product, without negatively
influencing the transmission properties.
In order to improve the light transmission properties of the final
packaging, i.e. decreasing the transmission of the portion of visible and UV
light that is detrimental to the shelf life of light sensitive products, such as
dairy products, an amount of iron oxide or mixed metal oxides consisting of Ni,
Fe, Mn, Ti,Co, Cr, Cu, Sn, Sb and combinations can be added. Examples are
Pigment Black 11 (CI number 77499), Pigment Black 12 (CI number 77543),
Pigment Black 28 ((CI number 77428) or Pigment Black 30 (CI number 77504)
and mixtures thereof. These compounds can be commercially purchased at
pigment producing companies e.g., the Shepherd Colour Company, Cincinnati,
USA. This amount can be up to 3 wt.%. The preferred amount is between 0.1
and 1 wt.%. Other components that may be used in the concentrate are
graphite and carbon black.
The concentrate can be prepared using suitable methods known to
the skilled person. Preferred methods are based on melt blending the various
components at a temperature, whereby the polyester(s) and the waxy
compound are in molten form. The melt that is thus obtained is subsequently
brought in suitable solid form. Melt blending can suitably be done in an
extruder and cutting the cooled extrudate into a suitably sized product.
The invention is also directed to the use of the concentrate in
colouring packaging, including bottles, that is prepared from polyesters, more
in particular PET, PBT and PEN by blow moulding a preform into a suitably
shaped product. The concentrate is incorporated in the polyester from which
the preform is made, generally by feeding the concentrate in particle form,
together with the polyester (and optional other additives), to the extruder on
which the preforms are produced. The preforms are then, in a separate step,
blow moulded in the final packaging (bottle). The conditions for preparing the
preform and for blow moulding the final product are the conventional
conditions, which are easily determined by the skilled person, based on the
various parameters involved, such as type and size of bottle, type of polyester,
etc.
The amount of concentrate that is added to the polyester may vary
between wide ranges. Preferred amounts are up to 15 wt.% of the concentrate,
based on the combined weight of the polyester and the concentrate. More
preferred amounts are between 2.5 and 15 wt.%. Higher amounts than 15 wt.%
may be used, but are generally not necessary, as can be seen from the
Examples.
The invention now elucidated on the basis of the following, non-
limiting examples.
EXAMPLES
A mixture of 3490 g Ti02, 1250 g PET resin (TV of 0.60) 250 g GMS
(glycerol monostearate) and 10 g of Pigment black 12 (CI number 77543) was
mixed and compounded/granulated on a laboratory extruder (APV 19mm twin
screw) and temperature profile between 270 and 240 C at 300 rpm.
The resulting granulate was used to prepare bottles via injection
moulding (Boy 50T2) and stretch blow moulding (SP 2000B B/J from Suyash
PET International Ltd.) at several concentrations (1,2,4,6,8,10,12 wt%).
A commercial 60% Ti02 masterbatch was taken as a standard for
comparison. The masterbatch was used to prepare bottles via injection
moulding using the same equipment as described above at several
concentrations (1,2,6,12,17.5,22.5 and 29 wt%).
The transmission curves from 200-700 nm of the blown bottles were
collected using a Cary 5000 equipped with an integrating sphere. The
%transmission at 550 nm was taken as a function of dosing level. Results are
shown in Figure 1. As can be seen, the amount of light transmitted using the
concentrate of the invention (UHT white) is significantly lower, at lower dosing
levels, than using the standard masterbatch.
COMPARATIVE EXAMPLES
In order to compare results from US patent 6,469,083 with the
results from the present invention two samples were prepared consisting of
70.0 parts by weight of an additive package consisting solely of Ti02 pigment
with 30.0 parts by weight of a carrier.
Sample R7923, the components pentaerythritol ester of partially
hydrogenated wood rosin 20.0% (wt) (Hercules FORAL 105); core-shell polymer
22.0% (wt) (Rohm & Haas PARALOID EXL-2300) thermoplastic PET (SIV =
0.94 dL/g) 58.0% (wt) (Die Mossi & Ghisolfi-Gruppe TRAYTUF T95).
Sample R7924, the components pentaerythritol ester of partially
hydrogenated wood rosin 20.0% (wt) (Hercules FORAL 105); core-shell polymer
22.0% (wt) (Rohm & Haas PARALOID EXL-2600) thermoplastic PET (SIV =
0.94 dL/g) 58.0% (wt) (Die Mossi & Ghisolfi-Gruppe TRAYTUF T95).
In both cases, the components were dry-blended and
compounded/granulated on a laboratory extruder (APV 19mm twin screw) with
a temperature profile between 270 and 240 C at 300 rpm. The resulting
granulate was used to prepare bottles via injection moulding (Arburg
Allrounder 320,) and stretch blow moulding (SP 2000B B/J from Suyash PET
International Ltd.) at 10 and 14%. For comparison, the sample material UHT
White described in Example 1 was dosed at 5 and 10%.
Figure 2 shows the results from transmission measurements from
300-700 nm of the blown bottles, which were collected using a Cary 5000
equipped with an integrating sphere. As can be seen, the amount of light
transmitted using the concentrate of the invention (UHT white) is significantly
lower, at lower dosing levels, than of the comparative samples R7923 and
R7924.
Claims
1. Titanium dioxide based colour concentrate, suitable for colouring
polyester materials, said concentrate comprising, based on the weight of the
concentrate, more than 50 % of titanium dioxide, up to 20 % of at least one wax
selected from the group of glycerol monostearate, hydrogenated castor oil and
polyethoxylated glycols, and up to 30 % of polyester.
2. Colour concentrate according to claim 1, wherein the amount of
titanium dioxide in the concentrate is between 60 and 75 wt.%.
3. Concentrate according to claim 1 or 2, wherein the amount of wax is
between 1 and 10 wt.%.
4. Concentrate according to claim 1-3, wherein the amount of polyester
is at least 5 wt.%.
5. Concentrate according to claim 1-4, wherein the said polyester is
polyethylene-terephtalate having an intrinsic viscosity (IV) between 0.2 and
1.2, preferably between 0.2 and 0.65.
6. Concentrate according to claim 1-5, wherein further iron oxide,
mixed metal oxide, graphite, carbon black or combinations thereof are present
in the concentrate, preferably in an amount of up to 3 wt.%.
7. Concentrate according to claim 1-6, wherein the mixed oxide is
selected from Pigment Black 11 (CI number 77499), Pigment Black 12 (CI
number 77543), Pigment Black 28 ((CI number 77428) or Pigment Black 30 (CI
number 77504) and mixtures thereof.
8. Concentrate according to claim 1-7, wherein the concentrate
additionally contains a further polyester, preferably selected from the group of
polyethylene-terephtalate, cyclohexane dimethanol/PET copolymer (PETG),
polyethylene naphthalate (PEN), polybutylene terephthalate (PBT), and
mixtures thereof.
9. Use of a concentrate according to claim 1-8, for colouring polyester,
such as polyethylene terephtalate, polybutylene terephtalate or polyethylene
natphalate, preferably polyester preforms for bottles or other containers.
10. Use according to claim 9, wherein the said bottles are for storing
light sensitive products, such as milk or milk products.
11. Process for preparing polyester bottles suitable for storing milk or
milk products and having a low transmission for visible and UV light, said
process comprising producing a preform for said bottles from the polyester and
the concentrate of claims 1-8, and blow moulding the preform into a bottle.
12. Process according to claim 11, wherein the concentrate is used in an
amount of 2.5 to 15 wt.% of the weight of the polyester.
13. Bottle produced by the process of claims 11 or 12.
The invention is directed to a titanium dioxide based colour
concentrate, suitable for colouring polyester materials, said
concentrate comprising, based on the weight of the concentrate, more
than 50 % of titanium dioxide, up to 20 % of at least one wax selected
from the group of glycerol monostearate, hydrogenated castor oil and
polyethoxylated glycols, and up to 30 % of at least one polyester.

Documents:

4855-KOLNP-2008-(03-03-2014)-ANNEXURE TO FORM 3.pdf

4855-KOLNP-2008-(03-03-2014)-CORRESPONDENCE.pdf

4855-KOLNP-2008-(03-03-2014)-OTHERS.pdf

4855-KOLNP-2008-(04-06-2014)-ANNEXURE TO FORM 3.pdf

4855-KOLNP-2008-(04-06-2014)-CORRESPONDENCE.pdf

4855-KOLNP-2008-(12-11-2012)-ANNEXURE TO FORM 3.pdf

4855-KOLNP-2008-(12-11-2012)-CORRESPONDENCE.pdf

4855-KOLNP-2008-(13-01-2014)-ANNEXURE TO FORM 3.pdf

4855-KOLNP-2008-(13-01-2014)-CORRESPONDENCE.pdf

4855-KOLNP-2008-(16-05-2012)-CORRESPONDENCE.pdf

4855-KOLNP-2008-(16-05-2012)-FORM-3.pdf

4855-KOLNP-2008-(16-08-2013)-ANNEXURE TO FORM 3.pdf

4855-KOLNP-2008-(16-08-2013)-CORRESPONDENCE.pdf

4855-KOLNP-2008-(18-04-2013)-CORRESPONDENCE.pdf

4855-KOLNP-2008-(18-04-2013)-FORM 3.pdf

4855-KOLNP-2008-(30-04-2014)-CLAIMS.pdf

4855-KOLNP-2008-(30-04-2014)-CORRESPONDENCE.pdf

4855-KOLNP-2008-(30-04-2014)-DRAWINGS.pdf

4855-KOLNP-2008-(30-04-2014)-FORM-1.pdf

4855-KOLNP-2008-(30-04-2014)-FORM-3.pdf

4855-KOLNP-2008-(30-04-2014)-FORM-5.pdf

4855-KOLNP-2008-(30-07-2012)-CORRESPONDENCE.pdf

4855-kolnp-2008-abstract.pdf

4855-kolnp-2008-claims.pdf

4855-KOLNP-2008-CORRESPONDENCE 1.2.pdf

4855-KOLNP-2008-CORRESPONDENCE-1.1.pdf

4855-kolnp-2008-correspondence.pdf

4855-kolnp-2008-description (complete).pdf

4855-kolnp-2008-drawings.pdf

4855-kolnp-2008-form 1.pdf

4855-kolnp-2008-form 2.pdf

4855-KOLNP-2008-FORM 26.pdf

4855-kolnp-2008-form 3.pdf

4855-kolnp-2008-form 5.pdf

4855-kolnp-2008-international publication.pdf

4855-kolnp-2008-international search report.pdf

4855-KOLNP-2008-OTHERS.pdf

4855-kolnp-2008-pct priority document notification.pdf

4855-kolnp-2008-pct request form.pdf

4855-kolnp-2008-specification.pdf


Patent Number 263842
Indian Patent Application Number 4855/KOLNP/2008
PG Journal Number 48/2014
Publication Date 28-Nov-2014
Grant Date 24-Nov-2014
Date of Filing 01-Dec-2008
Name of Patentee HOLLAND COLOURS N.V.
Applicant Address HALVEMAANWEG 1, 7323 RW APELDOORN
Inventors:
# Inventor's Name Inventor's Address
1 DE JAGER, ANDRIES MARIA HALVEMAANWEG 1 7323 RW APELDOORN
2 WERINK, JOHAN JOZEF MARINUS HALVEMAANWEG 1 7323 RW APELDOORN
3 ROELOFS, JULES CASPAR ALBERT ANTON HALVEMAANWEG 1 7323 RW APELDOORN
4 STOOP, JEROEN HALVEMAANWEG 1 7323 RW APELDOORN
PCT International Classification Number C08K 3/22,B29C 49/00
PCT International Application Number PCT/NL2007/050197
PCT International Filing date 2007-05-04
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 06076006.3 2006-05-05 EUROPEAN UNION