Coating layer for paper and board using dissolved cellulose

Abstract

According to an example aspect of the present invention, there is provided method for manufacturing a barrier layer on top of a paper or carton board from dissolved cellulose, which combines the benefits of the raw material, improved casting method and replacement of sulphuric acid with sodium carbonate or sodium hydrogen carbonate in regeneration bath.

Claims

1. A method for manufacturing a coating layer on top of a paper or carton board from a dissolved cellulose material, wherein the method comprises at least the steps of: preparing a dissolved cellulose solution, casting the dissolved cellulose solution from a nozzle to air and to a support, forming a film, coated paper or coated carton board from the casted dissolved cellulose solution, leading the formed film, coated paper or coated carton board into a regeneration coagulation bath comprising sodium carbonate or sodium hydrogen carbonate, and washing and drying of the film, coated paper or coated carton board.

2. The method according to claim 1, wherein the dissolved cellulose material is selected from dissolving pulp, bleached hard wood pulp, bleached softwood pulp and recycled fibres.

3. The method according to claim 1, wherein the casting is carried out in ambient air.

4. The method according to claim 1, wherein the casting is carried out onto a metallic support, when preparing a stand-alone film.

5. The method according to claim 1, wherein there is an air gap between the nozzle and the support.

6. The method according to claim 1, wherein the regeneration coagulation bath comprises 20 to 30 wt-% of Na.sub.2CO.sub.3 or NaHCO.sub.3 and 1 to 10 wt-% of NaOH.

7. The method according to claim 1, wherein the regeneration and coagulation is carried out at a temperature of about 30 C. when using sodium carbonate and at a temperature of about 40 C. when using sodium hydrogen carbonate.

8. The method according to claim 1, wherein the regeneration and coagulation is carried out in a bath comprising approximately 24 wt-% Na.sub.2CO.sub.3 and 4 wt-% NaOH at temperature of 30 C., or 24 wt-% NaHCO.sub.3 and 4 wt-% NaOH at temperature of 40 C.

9. The method according to claim 1, wherein the coating layer of dissolved cellulose is manufactured on top of at least one surface of the paper or carton board, wherein the at least one surface is fibrous and in a form of a web.

10. The method according to claim 1, wherein the process manufactures a continuous coating layer.

11. The method according to claim 1, further comprising placing the formed film, coated paper or coated carton board into a glycerol bath.

12. A coating layer on top of at least one surface of a paper or carton board, wherein the coating layer has been manufactured from dissolved cellulose according to the method of claim 1.

Description

EMBODIMENTS

[0015] The present technology provides a method for coating (for example by slot die or cast coating) a layer, such as a continuous layer of dissolved cellulose on top of paper or carton board followed by regeneration, washing and drying and thereby creating a coating layer, such as a barrier layer against oxygen, water vapour, loose water and grease. Regeneration is preferably carried out in a coagulation bath, where the dissolved cellulose dopes enter into sodium carbonate or sodium hydrogen carbonate solutions. The casting quality and control is improved by casting of the dissolved cellulose from nozzle to air and to support (such as for example paper or carton board) instead of nozzle to liquid.

[0016] FIG. 1 is a chart disclosing the tensile strength (N) of the standalone films in sodium carbonate or sodium hydrogen carbonate solutions. The results show that using glycerol results in higher tensile strength, 70 second bath residence time or even lower is enough for the desired effect, when washed after glycerol bath tensile appears unaffected, and that Na.sub.2CO.sub.3 and NaHCO.sub.3 regenerated samples have higher tensile strength compared to H.sub.2SO.sub.4 regenerated samples. Washing after glycerol bath should follow dipping into 100% glycerol bath. In trials more beneficial was to use 10%/90% glycerol/water bath without washing.

[0017] FIG. 2 is a chart disclosing the modulus (MPa) of the standalone films in sodium carbonate or sodium hydrogen carbonate solutions. The results show that using glycerol results in higher modulus, 70 seconds bath time or even lower is enough for the desired effect, when washed after glycerol bath modulus appears unaffected, and that Na.sub.2CO.sub.3 and NaHCO.sub.3 regenerated samples have higher modulus compared to H.sub.2SO.sub.4 regenerated samples.

[0018] FIG. 3 is a chart disclosing the strain at break (%) of the standalone films in sodium carbonate or sodium hydrogen carbonate solutions. The results show that glycerol increases strain at break, and that overall values are high.

[0019] FIG. 4 is a chart disclosing the drying tension after levelling (N/m) of the standalone films. The results show that glycerol decreases drying tension significantly, and the effect of glycerol after washing is seen clearly. Also hard feel (i.e. softer grip) supports the observation that wash bath after glycerol bath does not remove all glycerol.

[0020] FIG. 5 is a chart disclosing the shrinkage vs. modulus (%) of the standalone films. The results show that glycerol decreases shrinkage significantly, and the effect of glycerol after washing is seen clearly. Values are measured in CD-direction of 24 mm wide strips.

[0021] FIG. 6 is a chart disclosing the drying tension (N) of the standalone films. The results show that drying is fast, at best only 60 seconds. Glycerol slows down the time required for tension to level off. Tension curves differ and the effect of glycerol consistency is seen clearly. In addition, steepness of the curves is different and when water is more than 50% in glycerol, there is a drop of tension curve raising stage.

[0022] The present technology is based on specific combination of three main aspects: 1) coating a layer of dissolved cellulose on top of paper or carton board, followed by regeneration, washing and drying 2) wherein the regeneration is preferably carried out in a coagulation bath comprising sodium carbonate or sodium hydrogen carbonate solutions, and 3) casting from nozzle to air and to support.

[0023] One embodiment is a method for manufacturing a coating layer on top of a paper or carton board from a dissolved cellulose material, comprising at least the steps of: [0024] preparing a dissolved cellulose solution, [0025] casting the dissolved cellulose solution from a nozzle to air and to a support, [0026] forming a film, coated paper or coated carton board from the casted dissolved cellulose solution, [0027] leading the formed film, coated paper or coated carton board into a regeneration coagulation bath comprising sodium carbonate or sodium hydrogen carbonate, and [0028] washing and drying of the film, coated paper or coated carton board.

[0029] The dissolved cellulose solution may be prepared for example by the method disclosed in WO 2009/135875 A1.

[0030] According to one embodiment, the described method is used for manufacturing a barrier layer.

[0031] According to one embodiment, the dissolved cellulose material is selected from dissolving pulp, bleached hard wood pulp, bleached softwood pulp and recycled fibres demonstrating impact of hemicellulose and inorganic impurities.

[0032] According to one embodiment, the casting is carried out in ambient air.

[0033] According to one embodiment, the casting is carried out onto a metallic support, such as onto a metallic flat belt or roller surface. Casting onto metallic support (belt of roller) enables better control of casting quality and makes it essentially easier to solve blocking issues, start-ups and cleaning procedures. CD- and MD-profile thickness measurements are possible right after casting, which enhances the quality of the end-product. In addition, the casting unit material may be less acid durable. Furthermore, work safety is improved as lifting and lowering of slot die into acid regeneration bath is not needed. This embodiment is useful for example when preparing stand alone films.

[0034] In one embodiment, there is an air gap between the nozzle and the support, such as below one millimetre. Casting from slot using a sub one millimetre gap through air into preferred metallic type belt or roller without the need to cast directly into regeneration liquid has the advantages discussed above.

[0035] In one embodiment, regeneration coagulation bath comprises 20 to 30 wt-% of Na.sub.2CO.sub.3 or NaHCO.sub.3 and 1 to 10 wt-% of NaOH.

[0036] In one embodiment, the regeneration and coagulation is carried out at a temperature of about 30 C. when using sodium carbonate and at a temperature of about 40 C. when using sodium hydrogen carbonate.

[0037] Preferably, instead of typical 10% sulphuric acid, coagulation of standalone films or dissolved cellulose coated paper or carton board is coagulated in approximately 24 wt-% Na.sub.2CO.sub.3 and 4 wt-% NaOH at 30 C. or in 24 wt-% NaHCO.sub.3 and 4 wt-% NaOH at 40 C.

[0038] According to one embodiment, the coating layer, such as a barrier coating layer, of dissolved cellulose is manufactured on top of at least one surface of the paper or carton board, wherein the surface is preferably fibrous and in a form of a web. Thus, at least one surface of the paper or carton board is coated, which means that the coating layer can exist either on one outer surface, both outer surfaces or even in between different surface layers. In the latter embodiment, the coating layer can perform as a gluing layer for multi-layered fibrous structures. Such coating layer manufactured by the herein disclosed method on top of at least one surface of a paper or carton board belongs to the scope of the present invention.

[0039] According to one embodiment, it is preferred to use a plasticizer generally suitable for different cellulose materials, such as glycerol.

[0040] Reference throughout this specification to one embodiment or an embodiment means that a particular feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment of the present invention. Thus, appearances of the phrases in one embodiment or in an embodiment in various places throughout this specification are not necessarily all referring to the same embodiment. Where reference is made to a numerical value using a term such as, for example, about or substantially, the exact numerical value is also disclosed.

[0041] As used herein, a plurality of items, structural elements, compositional elements, and/or materials may be presented in a common list for convenience. However, these lists should be construed as though each member of the list is individually identified as a separate and unique member. While the forgoing examples are illustrative of the principles of the present invention in one or more particular applications, it will be apparent to those of ordinary skill in the art that numerous modifications in form, usage and details of implementation can be made without the exercise of inventive faculty, and without departing from the principles and concepts of the invention. Accordingly, it is not intended that the invention be limited, except as by the claims set forth below.

[0042] The verbs to comprise and to include are used in this document as open limitations that neither exclude nor require the existence of also un-recited features. The features recited in depending claims are mutually freely combinable unless otherwise explicitly stated. Furthermore, it is to be understood that the use of a or an, that is, a singular form, throughout this document does not exclude a plurality.

INDUSTRIAL APPLICABILITY

[0043] The present technology provides coatings, such as oxygen, water vapour and grease barrier coatings for paper and carton boards used in various end-products, which coatings are manufactured from dissolved cellulose with unique unit operations. The starting material complies with the current EU-plastic related regulations and is not qualified as a plastic.

EXAMPLES

Example 1

[0044] A stand alone film was manufactured in lab scale from regenerated cellulose solution (Biocelsol dissolving method) having solids content of 6.44% and ball drop viscosity (ball dropping time for 200 mm; D.sub.pipe=D.sub.ball=, 130 mg; modified ASTM D1343-95) at 20 C. 66 seconds was casted on 1.5 mm thick stainless steel ANSI 304 plate using an Ericsson lab coater with a comb having a 400 micron casting gap in room temperature. After casting the stainless steel plate was sunk into 10% sulphuric acid bath in room temperature for two minutes to regenerate the casted solution. After 90 seconds the casted cellulose solution began to detach from steel plate surface and after 120 seconds it was carefully transferred to water bath with running water for ten minutes. After ten minutes the sheet was removed from water bath and placed to milliq water bath in room temperature. Next day the wet sheet was placed on glass plate on cut to 15 mm wide strips and again placed into milliq water bath. Prior to tensile measurements each strip was placed into 5% glycerol/water mixture for 70 seconds and measured immediately using Lloyd tensile tester with 100N force cage to evaluate wet tensile properties and effect of plasticizer.

Example 2

[0045] A stand alone film having final thickness of 30 microns was manufactured in lab scale. A regenerated cellulose solution (Biocelsol dissolving method) having solids content of 6.44% and ball drop viscosity (ball dropping time for 200 mm; D.sub.pipe=D.sub.ball=, 130 mg; modified ASTM D1343-95) at 20 C. 66 seconds was casted on 1.5 mm thick stainless steel ANSI 304 plate using an Ericsson lab coater with a comb having a 400 micron casting gap in room temperature. After casting the stainless steel plate was sunk into 24% sodium hydrogen carbonate dissolved in 4% NaOH water solution bath heated to 40 C. temperature for two minutes to regenerate the casted solution. After 110 seconds the casted cellulose solution began to detach from steel plate surface and after 120 seconds it was carefully transferred to water bath with running water for ten minutes. After ten minutes the sheet was removed from water bath and placed to milliq water bath in room temperature. Next day the wet sheet was placed on glass plate on cut to 15 mm wide strips and again placed into milliq water bath. Prior to tensile measurements each strip was placed into 5% glycerol/water mixture for 70 seconds and measured immediately using Lloyd tensile tester with 100N force cage to evaluate wet tensile properties and effect of plasticizer.

Example 3

[0046] A stand alone film having final thickness of 28 microns was manufactured in lab scale. A regenerated cellulose solution (Biocelsol dissolving method) having solids content of 6.44% a regenerated cellulose solution (Biocelsol dissolving method) having ball drop viscosity (ball dropping time for 200 mm; D.sub.pipe=D.sub.ball=, 130 mg; modified ASTM D1343-95) at 20 C. 66 seconds was casted on 1.5 mm thick stainless steel ANSI 304 plate using an Ericsson lab coater with a comb having a 400 micron casting gap in room temperature. After casting the stainless steel plate was sunk into 24% sodium hydrogen carbonate dissolved in 4% NaOH water solution bath heated to 40 C. temperature for two minutes to regenerate the casted solution. After 110 seconds the casted cellulose solution began to detach from steel plate surface and after 120 seconds it was carefully transferred to water bath with running water for ten minutes. After ten minutes the sheet was removed from water bath and placed to milliq water bath in room temperature. Next day the wet sheet was placed into 5% glycerol/water mixture for 70 seconds and after placed on specially designed drying apparatus. The sheet was attached using magnets from all sides to steel frame open from bottom and top side allowing the water to evaporate freely and preventing shrinkage during drying. The sheet was let to dry in lab conditions (23 C., 50% RH) for 24 hours prior to cutting to 15 mm wide strips and measured using Lloyd tensile tester with 100N force cage.

Example 4

[0047] Regenerated cellulose solution (Biocelsol dissolving method) having solids content of 6.7% was casted on carton board containing an unbleached and pigmented outer layers with total grammage of 185 g/m.sup.2. Using an Ericsson lab coater combs having a 200 and 400 micron casting gap carton board sheets were coated in room temperature onto pigmented side. After casting, carton boards sheets were placed into 24% sodium hydrogen carbonate dissolved in 4% NaOH water solution bath heated to 40 C. for two minutes to regenerate and attach the casted solution to carton board surface. After 120 seconds board sheets were transferred to water bath with running water for ten minutes. After ten minutes the sheets were removed from water bath and placed between blotting papers in a table top lab scale dryer and drying in approximately 80 C. degrees heat until dry. After 200 micron and 400 micron wet layer coated sheets were conditioned in standard lab conditions for 48 hours and oxygen barrier of sheets was measured. Oxygen barrier for thinner coating was 11.91.4 cc/(m.sup.2day) and for thicker coating layer 3.51.1 cc/(m.sup.2day) which correspond to dry coating layer of approximately 12 to 16 microns and 26 to 30 microns.