Patent Application
20120283374
The invention relates to an aqueous dispersion of hybrid particles consisting of organic or inorganic pigment particles and organic nano-particles attached to the surface of the pigment particles, the nano-particles having a particle size between 2 and 200 nanometer. The invention further relates to a process for preparing such a dispersion to a coating composition for coating paper and similar material and to the use of the composition in coating paper and similar material.
In EP-A-1 422 248 an aqueous dispersion containing nano-particles has been described, which aqueous dispersion is used as a paper sizing composition, especially with the aim to improve the surface characteristics of the paper or the like.
However for applications on porous substrates such as e.g. paper, these nano-particles are not very effective as they have the tendency to disappear in the pores of the substrate during application, especially under high pressure of a blade or a roll. Mixing the nano-particles with a carrier of sufficient size, normally called pigment in this art, has not given any substantial improvement as the nano-particles still have the tendency to disappear in the pores of the substrate.
It is an object of the invention to provide an aqueous dispersion whereby these above mentioned problems can be avoided or at least the result can be improved.
This object is obtained by means of the aqueous dispersion according to claim 1.
By attaching the nano-particles to a bigger pigment-particle it has been obtained that the nano-particles are maintained at the surface level of the substrate as the pigment particle have such a size that they are not disappearing in the pores, but are kept close to the surface level of the substrate.
A process for obtaining such an aqueous dispersion in which the nano-particles are attached to the surface of the pigment particles consists of preparing the nano-particles in the presence of such pigment particles.
The smaller particles are to a large extent physically or chemically attached to the larger particles. It has been found that the produced nano-particles in the presence of larger particles have a smaller average size than when produced as such. As a result the hybrid particles have a very good stability in water, much better than a blend of the nano-particles with the larger particles. The hybrid particles further show a better adhesion to substrates like aluminum, in a coating formulation less binder is necessary, they provoke less dust formation after application and they give less settlement on the rolls during the application when compared with a blended composition of comparable materials. The hybrid particles have a hydrophobicity which is similar to the one of the nano-particles, while for the blended material the hydrophobicity is more an average of the blended materials. In case of styrene maleimide co-polymers (SMI) as nano-particles, its high hydrophobicity allows a high fraction of repulpable binder in its formulation without affecting the water fastness of the resultant paper. Furthermore, the resultant coatings have a better gloss and a lower coefficient of friction.
The hybrid particles according to the present invention can be obtained by dissolving a co-polymer of maleic anhydride with a vinyl monomer in water by adding a R—NH2 compound, R being H, alkyl with 1-18 C-atoms or aryl, and to heat up the resultant mixture in the presence of larger particles to make the imides. The formed imides are hydrophobic and the polymeric particles will settle down on the larger particles.
The object of the invention is to provide a method with which a better quality dispersion can be obtained. This object is achieved according to the invention in that the reaction is carried out in the presence of one or more organic or inorganic pigments, the pH being set to a value of preferably 5 to 9 and the temperature to preferably 110-180° C., until a degree of imidisation d at least 35% preferably at least 50%, is obtained.
The shear load and visco-elasticity are much lower during the imidisation phase if a carrier pigment is added. The SMI particles precipitated on the carrier may have a size varying between 2 and 200 nanometers but mostly between 2 and 50 nanometers, and have an extremely monodispersive behaviour on the carrier pigment. The carrier pigment is always larger than the SMI, and for practical reasons it is limited from 500 nanometers to approx. 100 microns.
The reaction is preferably conducted at a pH of 5.5-8, the best results being obtained at a pH of 5.5-7.
For the temperature at which the reactions are carried out preference is given to 120-160° C., the best results being obtained at 140-150° C.
Although a product with a degree of imidisation of 20% already gives some results, dependent upon the hydrophobic characteristics of the compound R—NH2 the reactions are preferably continued until a degree of imidisation of at least 35% is achieved, the best results being obtained at a degree of imidisation of 80% or more.
The invention relates in principle to the difficulty with which nano-particles of pure styrene-maleimide can be applied to substrates such as paper and others, where the nano-particles are always smaller than the initial porosity of the substrate. By allowing these nano-particles to precipitate during their formation onto another base pigment, the possibility is created of maintaining these nano-particles on the surface to the optimum degree, whilst the gloss, printability and colour reproduction of the paper are clearly improved. At the same time the costs are reduced since 70% less SMI is required to coat the same surface. Finally, the nano-particles are applied to an organic or inorganic substrate and the particles retain their non-film-forming properties. Even on very smooth, dense structures such as aluminum foil, positive results have been achieved. In the case of aluminum foils with low gram weights of approx. 6 gr/m2, the number of pinholes could be substantially reduced by the application of the dispersion until complete elimination The latter means a considerable saving in the consumption of aluminum foils in packaging materials, since the same properties of steam tightness could only be obtained if aluminum foil with a gram weight of at least 12 g/m2 was used. The term pigment as used in this description is a term normally used in paper industry for designating a filler material, and its meaning is not restricted to a colouring agent as such.
A dispersion, obtained by the method according to the invention, is applied in both coated (coater) and non-coated (film press) office/and copy paper (coated and non-coated paper) and offset paper which can also be provided with a glossy layer. After application of the dispersion to the paper, use is made of a calander to provide the paper with a gloss effect. The pressure and the number of passages to obtain the same gloss as in traditionally produced paper are lower, with the result that the surface is less damaged and the strength of the paper is better retained. This also counteracts possible an uneven mottling absorption of ink. Another object of this invention is to a dispersion that is suitable for paper coating, the particles of which do not show any film formation during calandering, but whose structure is retained. This has a direct influence on gloss, particularly after printing.
Suitable pigments may be organic or inorganic. Examples of inorganic pigments include carbon black and titanium oxide. Examples of organic pigments include phthalocyanines, anthraquinones, perylenes, carbazoles, monoazo- and disazobenzimidazolones, isoindolinones, monoazonaphthosl, diarylidepyrazolones, rhodamines, indigoids, quinacridones, diazopyranthrones, dinitranilines, pyrazolones, dianisidines, pyranthrones, tetrachloroisoindolinones, dioxazines, monoazoacrylides, and anthrapyrimidines.
Commercial examples of organic pigments include those described in The Colour Index, Vols. 1-8, Society of Dyers and Colourists, Yorkshire, England; including, for example Pigment Blue 1, Pigment Blue 15, Pigment Blue 15:1, Pigment Blue 15:2, Pigment Blue 15:3, Pigment Blue 15:4, Pigment Blue 15:6, Pigment Blue 16, Pigment Blue 24, and Pigment Blue 60 (blue pigments); Pigment Brown 5, Pigment Brown 23, and Pigment Brown 25 (brown pigments); Pigment Yellow 3, Pigment Yellow 14, Pigment Yellow 16, Pigment Yellow 17, Pigment Yellow 24, Pigment Yellow 65, Pigment Yellow 73, Pigment Yellow 74, Pigment Yellow 83, Pigment Yellow 95, Pigment Yellow 97, Pigment Yellow 108, Pigment Yellow 109, Pigment Yellow 110, 5 Pigment Yellow 113, Pigment Yellow 128, Pigment Yellow 129, Pigment Yellow 138, Pigment Yellow 139, Pigment Yellow 150, Pigment Yellow 154, Pigment Yellow 156, and Pigment Yellow 175 (yellow pigments); Pigment Green 1, Pigment Green 7, Pigment Green 10, and Pigment Green 36 (green pigments); Pigment Orange 5, Pigment Orange 15, Pigment Orange 16, Pigment Orange 31, Pigment Orange 34, Pigment Orange 36, Pigment Orange 43, Pigment Orange 48, Pigment Orange 51, Pigment Orange 60, and Pigment Orange 61 (orange pigments); Pigment Red 4, Pigment Red 5, Pigment Red 7, Pigment Red 9, Pigment Red 22, Pigment Red 23, Pigment Red 48, Pigment Red 48:2, Pigment Red 49, Pigment Red 112, Pigment Red 122, Pigment Red 123, Pigment Red 149, Pigment Red 166, Pigment Red 168, Pigment Red 170, Pigment Red 177, Pigment 15 Red 179, Pigment Red 190, Pigment Red 202, Pigment Red 206, Pigment Red 207, and Pigment Red 224 (red pigments); Pigment Violet 19, Pigment Violet 23, Pigment Violet 37, Pigment Violet 32, and Pigment Violet 42 (violet pigments); and Pigment Black 6 or 7 (black pigments).
The organic pigment is preferably selected from kaolin, talcum, mica, clay, Al2(OH)3, bentonites, zeolites, glass pearls, CaCO3, TiO2, sepeolites, silica, zirconium oxide, iron oxide or mixtures thereof.
This produces a dispersion which after application to the paper has no film formation during calendaring of the coated paper, and whose particle structure is retained. A very high solid content is achieved, even exceeding 65%.
In the method according to the invention the initial polymer is dissolved in an aqueous solution of a compound with the general formula R—NH2, where R is selected from the series H, alkyl with 1-18 C atoms and aryl. R is preferably hydrogen.
The initial polymer is also dissolved in the presence of a pigment or a mixture of pigments. During the imidisation reaction a dispersion aid may be added. Such a dispersion aid could e.g. be an alkali salt of styrene maleic anhydride copolymer.
The initial polymer with which the dispersion is prepared contains MZA monomeric units and vinyl monomers, preferably vinyl aromatic monomeric units. Suitable vinyl aromatic monomeric units are, for example, styrene and alpha methyl styrene. The initial polymer preferably contains styrene as monomeric units. Other vinyl monomers can be acrylates, methacrylates, ethylene, propylene, vinyl carbonate, vinyl acetate and mixtures thereof.
A copolymer containing vinyl aromatic monomeric units and MAA monomeric units can be prepared by known methods. An example of such a method for the preparation of a copolymer of MAA monomeric units and styrene is described by Hanson and Zimmerman, Ind. Eng. Chem., vol. 49, no. 11 (1957) pp. 1803-1807. The initial polymer preferably contains 22-50 mol % maleic acid anhydride monomeric units and 50-78 mol % styrene monomeric units. A dispersion can therefore be obtained from a polymer with a glass transition temperature of over 120° C., and the imidisation takes place relatively quickly.
The molecular weight of the initial polymer may vary within wide limits. An initial polymer preferably has a weighted average molecular weight of between 10,000 and 300,000 kg/kmol. Even more preference is given to a weighted average molecular weight of between 60,000 and 150,000 kg/kmol. In this way a dispersion can be prepared with a relatively high solid content.
In the method according to the invention the initial polymer can, for example, be introduced into an autoclave together with an aqueous solution of NH3 or an amine, whereupon the temperature is raised to at least 140° C. The molar ratio of maleic acid anhydride (MAA) monomeric units and NH3 or MAA and amine, is generally between 1:08 and 1:5, where as the pressure is so high that the aqueous solution will not boil.
The time required to imidise the MAA monomeric units in the initial polymer almost completely depends on the selected temperature, the reactor, the initial quantities and the like, and can be easily determined experimentally. The imidisation reaction can be stopped or at least substantially delayed by reducing the temperature to below 95° C.
In a preferred embodiment of the method the temperature is between 150 and 190° C. because at this temperature a very well defined dispersion, in terms of properties and composition, with a high reproducibility, can be obtained. The molar ratio of maleic acid anhydride (MAA) monomeric units and NH3 or MAA and amine is preferably approx. 1:1 as this results in the highest degree of conversion without the dispersion generating an unpleasant taste. Ammonia or an aliphatic amine is preferably used, which aliphatic amine is a primary amine. Examples of suitable amines are butylamine and stearyl amine. One advantage of the method according to the invention is that a dispersion can be produced by the method with a solid content of over 65% by weight.
The invention also relates to an aqueous dispersion of a Hybrid pigment polymer which contains maleic acid anhydride (MAA) monomeric units and vinyl aromatic monomeric units, characterised in that the MAA is almost completely imidised and the dispersion has a solid content of over 65% by weight.
The Pigment/SMA ratio at the beginning of the reaction is ideally 70 parts of pigment to 30 parts of SMA, after converting to SMI. The maximum limit for these Hybrid pigment-polymer dispersions is approx. 99 parts of inorganic pigment to 1 part of SMI, and the minimum limit is 1 part of inorganic pigment to 99 parts of SMI.
The aqueous dispersion preferably has a polymer whose vinyl aromatic monomeric units are styrene and the glass transition temperature exceeds 160° C.
A further advantage of the dispersion according to the invention is that it has a relatively narrow particle size distribution.
The invention relates in particular to compositions for sized paper and pigmented film press paper, which contain the dispersion according to the invention.
Compositions for paper sizing contain not only a dispersion obtainable by the method according to the invention, but also one or more of the usual additives. The composition according to the invention is preferably characterised in that the composition may contain as additives both latex and starch. Other binders such as polyvinylalcohol, polyvinylacetate, Hybrone (a name of a product as sold by DSM, the Netherlands) and proteins can be used as well.
The quantity of dispersion which contains the composition is preferably such that the quantity of pigment-polymer, i.e. the dry weight of hybrid pigment-polymer particles in the dispersion, is between 0.2 and 90% by weight related to the dry weight of the other normal additives. More preferably a composition for paper sizing and coating contains between 80 and 90% by weight of Hybrid pigment-polymer particles related to the dry weight of starch or latex. A composition may, for example, be prepared by adding to the solution of the other additives in water a certain quantity of the dispersion according to the invention.
The invention will now be explained with reference to examples, but is in no way limited to them.
The mean hydrodynamic radius of the polymer particles was determined by means of Photon Correlation Spectroscopy (PCS). The measurements were carried out with a unit from ALV-Laser Vertriebsgesellschaft mbH in Langen, Germany (Coherent Innova 90 ion-argon laser; the blue line was used (488 nm), output 50 mW). The signal was collected by means of a photon-multiplier from Thorn-Emi, fitted to an ALV/SP-86#053 laser goniometer (supply voltage of photon-multiplier approx. 1700 V, measuring angle 90°). The signal was processed by an ALV 5000 Multiple Tau digital correlator equipped with the ALV5000/E for Windows-software. The method of cumulant analysis is used to process the measured data, and the Stokes-Einstein relation is used to determine a hydrodynamic radius from the measured diffusion coefficient.
For the PCS measurement the samples were diluted in demineralised water previously filtered via a filter with filter openings having a diameter of 0.2 μm. The samples obtained after implementation of a method according to the embodiment were diluted 500 times (to a concentration of approx. 0.04% by weight of solid or stock), and the samples obtained after carrying out a Comparative Experiment were diluted 50 times to approx. 0.4% by weight of solid.
The measuring cell was flushed before the measurements with dust-free water, then three times with the sample solution to be measured. A number of samples deriving from the Comparative Experiments were unstable in water. To stabilise these samples a buffer was used with a pH 9 of 0.02 (Titrisol from Merck) or a 10−3 M aqueous NaOH solution. The results of the PCS measurements are indicated in the different tables.
The solid content (SC) was determined by means of an infrared dry/weighing unit of the type Mettler LP16/PM600. If there was any polymer remaining after the reaction it was filtered off via a paper filter (MN640m medium retention and filtration speed from Macherey-Nagel, Germany) before the solid content was determined. If necessary filtration was carried out before this via a metal screen with screen holes 250 μm wide. The solid content of the resulting filtrates, bright in appearance, was then determined by the method known to the person skilled in the art.
pH values were measured with a Knick 752 Cl, no. 051489 pH meter. The pH meter was calibrated at 20° C. with buffer solutions Wth a pH of 4.00 (citrate/HCl buffer), 7.00 and 9.00 respectively from Merck, and was fitted with a gas electrode (3M KCl). The pH of the samples was determined at 20° C.
Samples from Comparative Experiments were diluted, if the solid content was higher and hence also the viscosity, to a solid content of approximately 10% by weight. Dispersions were not diluted.
The degree of imidisation of the aqueous dispersions can be measured, for example, by means of Raman-FTIR spectroscopy by relating the intensity of absorptions to the intensity of the same absorptions measured for a fully imidised and fully de-imidised reference compound. Before calculations were carried out the signals were standardised to the absorption signals deriving from the aromate rings in the polymer chains. In the measurements carried out the following absorption bands were examined:
In a double wall oil heated reactor of 1 litre, in which a turbine agitator is placed, 442 grams of a 65% kaolin slurry (type SPS from IMERIS) are added, together with the make-up water, then topped up with 132 grams of crushed SMA. The SMA has an MAA content of 26% and a molecular weight of 80,000 kg/kmol, to which is added a 25% solution of NH3 in an MAA;NH3 ratio of 1:1. The temperature is brought to 160° C. and the speed of the agitator to 200 rpm. The pressure in the reactor is approx. 6 bars. After 4 hours a Hybrid pigment polymer dispersion with a solid content of approx. 61% by weight is formed with precipitated particles between 15 and 30 nm. The MAA in these particles is almost fully imidised. The Tg of the outermost layer of the Hybrid polymer pigment is between 185° C. and 200° C.
In a double wall oil heated reactor of 1 litre, in which a turbine agitator is placed, 203 grams of a 65% kaolin slurry (type SPS from IMERIS) are added, together with the make-up water, with 203 grams of Al(OH)3, then topped up with 122 grams of crushed SMA. The SMA has an MAA content of 26% and a molecular weight of 80,000 kg/kmol, to which is added a 25% solution of NH3 in an MAA;NH3 ratio of 1:1. Furthermore, a potassium salt of an SMA can be added as dispersing agent with a molecular weight of 1000 kg/kmol, with an MAA content of 48% (in this case it is not added). The K-salt:SMA ratio=0.03:1. The temperature is brought to 160° C. and the speed of the agitator to 200 rpm. The pressure in the reactor is approx. 6 bars. After 4 hours a Hybrid pigment polymer dispersion with a solid content of approx. 52% by weight is formed with precipitated particles between 10 and 25 nm. The MAA in these particles is almost fully imidised. The Tg of the outermost layer of the Hybrid polymer pigment is between 185° C. and 200° C.
The MAA in these particles is almost fully imidised (99%). The Tg of the polymer is between 185 and 200° C., pH between 5 and 9.
The dispersions from both examples display no film-forming properties if they applied to paper either with a blade or film press.
A dispersion has been prepared using a mixture comprising on the one hand a dispersion of the reaction product of SMA and NH3 in the same ratio as described in example I and kaolin.
From this picture it is clear that most pigment particles are not coated with the SMI- or MAA-particles but that these particles are much smaller and do not cover completely the surface of the carrier. Part of the SMI- or MAA-particles has disappeared in the pores of the carrier and part of the SMI- or MAA-particles is covered by pigment particles thereby rendering them ineffective.
The influence of the degree of imidisation is shown in the
From the pictures it is evident that at a lower imidisation degree the pigment particles are less covered and the SMI- or MAA-particles are less present at the surface.
Having described the invention in detail and by reference to preferred embodiments thereof, it will be apparent that modifications and variations are possible without departing from the scope of the invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 05016756.8 | Aug 2005 | EP | regional |
This application is a continuation of U.S. patent application Ser. No. 11/989,331 filed Apr. 18, 2008, entitled AQUEOUS DISPERSION OF HYBRID PARTICLES CONSISTING OF ORGANIC OR INORGANIC PIGMENT PARTICLES AND ORGANIC NANO-PARTICLES AND PROCESS FOR PREPARING THE SAME, which application claims the benefit of International Application No. PCT/EP2006/006922 filed Jul. 14, 2006, which claims the benefit of EP Application No. 05016756.8 filed Aug. 2, 2005. The entire contents of said applications are hereby incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 11989331 | Apr 2008 | US |
| Child | 13272347 | US |
