WO2015114195A1

WO2015114195A1 - Cross-laminated plywood production

Info

Publication number: WO2015114195A1
Application number: PCT/FI2014/050066
Authority: WO
Inventors: Anna Koski; Kati TAAVILA
Original assignee: Upm-Kymmene Wood Oy
Priority date: 2014-01-28
Filing date: 2014-01-28
Publication date: 2015-08-06
Also published as: PL3925775T3; EP3099485B1; EP3925775A1; EP3099485A4; FI3925775T3; EP3925775B1; ES2967244T3; DK3925775T3; DK3099485T3; ES2703229T3; PL3099485T3; EP3099485A1; FI12307U1; EP3446871A1

Abstract

The invention relates to a method for producing cross-laminated plywood, wherein method comprises applying an aqueous binder composition on at least one surface of at least one veneer, wherein the aqueous binder composition is prepared by using at least polymerizable substance and crosslinking agent, and wherein: at least 20 weight-% of the polymerizable substance originates from lignin; at least 50 % of the molecules in the binder composition have a molecular weight of above 3000 Da and at least 5 % of the molecules in the binder composition have a molecular weight of below 1000 Da; and the polydispersity index of the binder composition is 6 or higher. The invention further relates to cross-laminated plywood, to a binder composition and to uses thereof.

Description

CROSS-LAMINATED PLYWOOD PRODUCTION

FIELD OF THE INVENTION

The invention relates to a method for produc^¬ ing cross-laminated plywood, to cross-laminated ply^¬ wood, to an aqueous binder composition, and to different uses of the binder composition.

BACKGROUND OF THE INVENTION

Lignin is a natural polymer, which can be extracted from e.g. wood. As lignin is a natural biopol- ymer its use as a component in binder compositions in^¬ stead of synthetic materials has been investigated in order to come up with a more environmentally friendly composition. Especially, the ability to replace syn^¬ thetic phenol in final phenolic resins, such as phenol formaldehyde resin, has been the object of prior art.

Prior art discloses different types of binder compositions, such a phenolic glues, to be used with wood products. Examples of such glues include composi^¬ tions comprising phenol formaldehyde resin. Traditionally synthetic phenol formaldehyde resins are produced by polymerizing phenol and formaldehyde in the pres^¬ ence of a catalyst. Examples of such catalysts are so^¬ dium hydroxide (NaOH) and acids. The method for pro^¬ ducing phenol formaldehyde resin comprises adding for^¬ maldehyde in a stepwise manner to a phenol composition and thereafter rising the temperature of the formed composition up to 80 - 90 °C . The composition is cooked at this temperature until a desired viscosity of the formed resin or polymer chain length is reached .

Prior art recognizes the use of lignin for the purpose of decreasing the amount of synthetic phe^¬ nol in a resin composition. Lignin has previously been used for replacing phenol during the production of lignin-phenol-formaldehyde resin .

Prior art further recognizes the use of a binder composition for the production of plywood. There are different types of plywood, i.e. cross- laminated and laminated veneer lumber. Both types of plywood comprise multiple layers of thin wood assem^¬ bled with adhesives, but the grain direction is dif^¬ ferent in these two types of plywood.

The inventors have recognized a need for a bio-based binder composition having properties suita^¬ ble for specific purposes and especially for the pro^¬ duction of cross-laminated plywood.

PURPOSE OF THE INVENTION

The purpose of the invention is to provide a new type of method for producing cross-laminated ply^¬ wood and to provide a new type of cross-laminated ply^¬ wood. Further, the purpose of the invention is to pro^¬ vide an aqueous binder composition and to provide dif^¬ ferent uses thereof.

SUMMARY

The method for producing cross-laminated ply^¬ wood according to the present invention is characterized by what is presented in claim 1.

The cross-laminated plywood according to the present invention is characterized by what is present^¬ ed in claim 36.

The aqueous binder composition according to the present invention is characterized by what is pre^¬ sented in claim 61.

The uses of the binder composition according to the present invention are characterized by what is presented in claims 81 and 82, respectively. BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are included to provide a further understanding of the invention and constitute a part of this specification, illus^¬ trate embodiments of the invention and together with the description help to explain the principles of the invention. In the drawings:

Fig. 1 represents the results received from DCS measurements (chemical hardening) ;

Fig. 2 represents the results received from ABES measurements (mechanical hardening) ; and

Fig. 3 represents the results received from ABES measurements (operating window) .

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to a method for producing cross-laminated plywood, wherein the method comprises applying an aqueous binder composition on at least one surface of at least one veneer, wherein the aqueous binder composition is prepared by using at least polymerizable substance and crosslinking agent, and wherein:

- at least 20 weight-% of the polymerizable substance originates from lignin;

- at least 50 % of the molecules in the bind^¬ er composition have a molecular weight of above 3000 Da and at least 5 % of the molecules in the binder composition have a molecular weight of below 1000 Da; and

- the polydispersity index of the binder com^¬ position is 6 or higher.

The inventors of the present invention sur^¬ prisingly found out that a binder composition with the above specified properties enables a more flexible process for cross-laminated plywood production. Espe^¬ cially, it was found out that the so-called operating window, i.e. the time that can be used between apply^¬ ing the binder composition on the surface of a veneer before it is joined by pressing with another veneer, could be extended without compromising the final bond^¬ ing strength when using this kind of a binder composition. Without limiting the invention to any specific theory of why the above advantage can be achieved, it is to be considered that the rather high polydispersi- ty index together with the specific molecular weight distribution of the binder composition beneficially affects the properties of the bio-based binder compo^¬ sition such that the so-called operating window of the plywood production process can be extended.

The present invention further relates to cross-laminated plywood comprising at least two ve^¬ neers glued together with an aqueous binder composi^¬ tion, which is prepared by using at least polymeriza- ble substance and crosslinking agent, and wherein:

- at least 20 weight-% of the polymerizable substance originates from lignin;

- the polydispersity index of the binder com^¬ position is 6 or higher.

The inventors of the present invention sur^¬ prisingly found out that the cross-laminated plywood being produced by using the above specified binder composition has a good strength as a result of the fact that the used binder composition has been partly penetrated into the wood material and partly remained in the glue line. As the molecules of the binder com^¬ position having a lower molecular weight will penetrate into possible cracks or scratches on the surface and surface layers of the veneers treated with the binder composition, and as the molecules of the binder composition having a higher molecular weight will remain at the glue line, the seam or the interface be^¬ tween two veneers is strengthened compared to a situa^¬ tion where the binder composition would only remain in the glue line or where the binder composition would over-flow or over-penetrate into the treated veneers.

The present invention further relates to an aqueous binder composition, which is prepared by using at least polymerizable substance and crosslinking agent, wherein:

- at least 20 weight-% of the polymerizable substance originates from lignin;

- the polydispersity index of the binder com^¬ position is 6 or higher.

The present invention further relates to the use of the binder composition according to the present invention for producing cross-laminated plywood.

The present invention further relates to the use of the binder composition according to the present invention for gluing together at least two veneers.

In this specification, unless otherwise stat^¬ ed, the expression "aqueous binder composition" should be understood as a binder composition, which involves water .

In one embodiment of the present invention at least two veneers are glued together with the binder composition. In one embodiment of the present inven^¬ tion at least two veneers are glued together with the aqueous binder composition under the influence of hot pressing . In one embodiment of the present invention the veneer is made of softwood. In one embodiment of the present invention the veneer is made of hardwood.

In one embodiment of the present invention, the density of the wood material of the veneer is 320

- 750 kg/m³, and preferably 390 - 650 kg/m³. In one em^¬ bodiment of the present invention the density of the wood material of the veneer is 390 - 550 kg/m³ or 520

- 650 kg/m³. In one embodiment of the present inven^¬ tion the density of the wood material of the veneer is 450 - 570 kg/m³. The above density values are measured in accordance with standards SFS-EN 384 and ISO 3131 (SFS-EN 384 - Structural timber - Determination of characteristic values of mechanical properties and density (2010), and ISO 3131 - Wood - Determination of density for physical and mechanical tests (1975)).

In one embodiment of the present invention the veneer is selected from a group consisting of pine veneer, poplar veneer, beech veneer, aspen veneer, spruce veneer, and birch veneer. In one embodiment of the present invention the veneer is softwood veneer. In one embodiment of the present invention the veneer is spruce veneer or pine veneer. In one embodiment of the present invention the veneer is birch veneer. In one embodiment of the present invention the cross- laminated plywood comprises veneers of one or more wood material.

In one embodiment of the present invention the at least one veneer is manufactured by one of ro^¬ tary cutting, flat slicing, quarter slicing, half- round slicing, and rift cutting. These methods are known as such in plywood manufacturing, and different methods result in a slightly different visual appear^¬ ance of the veneer. Rotary cutting may also be re^¬ ferred to as turning or rotary turning. In one embodiment of the present invention, the at least one veneer is manufactured by rotary cutting. In one embodiment of the present invention, all the veneers used for producing the cross-laminated plywood, are manufac^¬ tured by rotary cutting. In one embodiment of the pre^¬ sent invention, at least 80 %, and preferably 100 %, of the veneers used for the production of the cross- laminated plywood are manufactured by rotary cutting.

Using rotary cutting for manufacturing the at least one veneer, cutting checks or lathe checks are formed in the veneer. Lathe checks create more surface area, which may result in over-penetration and dry-out of the binder composition at the glue-line. Furthermore, lathe checks may exhibit areas of weakness. Lathe checks caused by rotary cutting constitute an important factor in veneer quality. The larger and deeper the lathe checks, the lower the strength and the rougher the veneer surface. The bonding of lathe checks by the binder composition together contributes to improve the veneer mechanical properties. The in^¬ ventors of the present invention surprisingly found out that the binder composition according to the present invention advantageously affected the bonding of veneers to each other when applied on veneers produced by rotary cutting.

In one embodiment of the present invention the thickness of the at least one veneer is 0.5 - 4 mm, preferably 1 - 3.5 mm, and more preferably 1.3 - 3.0 mm. The thicknesses of the veneers used for the production of the cross-laminated plywood can be the same for each veneer or can vary from one veneer to another. In one embodiment of the present invention, the veneers of the cross-laminated plywood have one and the same thickness. In one embodiment of the pre^¬ sent invention, the veneers of the cross-laminated plywood have different thicknesses. In one embodiment of the present invention at least 20 % of the veneers of the cross-laminated plywood have a thickness which is at least 0.2 mm, and preferably at least 0.5 mm less or more than the thickness of the rest of the ve^¬ neers in the cross-laminated plywood. In one embodi^¬ ment of the present invention at least 20 % of the ve^¬ neers of the cross-laminated plywood have a thickness of 0.2 - 3.5 mm, and preferably 0.5 - 2 mm, less or more than the thickness of the rest of the veneers in the cross-laminated plywood. In one embodiment of the present invention all the veneers of the cross- laminated plywood are equally thick, with the preci^¬ sion of 0.2 mm.

The moisture percentage of the different ve^¬ neers used for producing the plywood can vary. In one embodiment of the present invention the average mois^¬ ture percentage of the veneers to be used for produc^¬ ing cross-laminated plywood before applying the binder composition thereon is 1 - 9, and preferably 2 - 6. The above moisture values are measured in accordance with standard SFS-EN 322 (Wood-based panels. Determi^¬ nation of moisture content (1993)).

In one embodiment of the present invention at least one veneer is modified by heat treatment, chemi^¬ cal treatment, mechanical treatment, or by a combina^¬ tion thereof. In one embodiment of the present inven^¬ tion at least one veneer is modified by chemical treatment. When the veneers are modified or pre- treated the dimensional stability thereof can be in^¬ creased .

The inventors also found out that the use of this kind of a binder composition allowed the use of veneers with varying properties for cross-laminated plywood production. It was found out that the binder composition enables the production of good quality cross-laminated plywood even when using a process and/or materials of variable standard. Without limit^¬ ing the invention to any specific theory of why the above advantage can be achieved, it is to be consid^¬ ered that the properties of the binder composition al- lowing a broad operating window in cross-laminated plywood production enables more flexibility in the production process as such.

The aqueous binder composition according to the present invention can be formed by different man^¬ ners. The aqueous binder composition according to the present invention can be formed by mixing lignin with a previously produced composition comprising cross- linking agent polymerized with e.g. synthetic polymer- izable substance. The binder composition according to the present invention can be formed by forming an aqueous composition comprising lignin, synthetic polymerizable substance and crosslinking agent, and by allowing polymerization reactions to take place be^¬ tween these reactant components under the influence of heating the composition.

In one embodiment of the present invention by varying the ratio of the amount of crosslinking agent to polymerizable substance, and especially the ratio of the amount of crosslinking agent, e.g. formalde^¬ hyde, to synthetic polymerizable substance, e.g. phe^¬ nol, the properties of the formed binder composition are varied. By adjusting the ratio, it is possible to vary the amount of linear and branched chains in the binder composition, thus also affecting the molecular weight distribution as well as the polydispersity in^¬ dex of the formed binder composition. Also the ratio of the amount of catalyst to polymerizable substance, e.g. phenol, affects the molecular weight distribution and polydispersity index. Also the amount of lignin used in the process affects the molecular weight dis^¬ tribution of the final binder composition. The temperature and time, as well as other process parameters, may also affect the properties of the binder composi^¬ tion. Further, the molecular weight distribution of the binder composition can also be determined or ana^¬ lyzed during the production thereof. The binder compo- sition production process can be stopped when the binder composition is found to have suitable properties, such as degree of condensation.

In one embodiment of the present invention the polymerizable substance comprises lignin and at least one compound selected from the class of phenols. In one embodiment of the present invention the polymerizable substance consists of lignin and at least one compound selected from the class of phenols. In one embodiment of the present invention the polymerizable substance comprises lignin and at least one of phenol, cresol, and resorcinol. In one embodi^¬ ment of the present invention the polymerizable sub^¬ stance consists of lignin and at least one of phenol, cresol, and resorcinol. In one embodiment of the pre^¬ sent invention the polymerizable substance comprises lignin and phenol. In one embodiment of the present invention the polymerizable substance consists of lig^¬ nin and phenol.

In one embodiment of the present invention the crosslinking agent is selected from a group of al^¬ dehydes. In one embodiment of the present invention the group of aldehydes comprises an aldehyde, a deriv^¬ ative of an aldehyde, an aldehyde forming compound and any combination thereof. In one embodiment of the pre^¬ sent invention the derivative of an aldehyde is hexa- methylenetetramine, paraformaldehyde or trioxane. In one embodiment of the present invention the crosslink^¬ ing agent is selected from a group consisting of an aromatic aldehyde, glyoxal, furfuryl alcohol, capro- lactam and glycol compounds. The aromatic aldehyde can be furfuryl aldehyde. In one embodiment of the present invention the crosslinking agent is an aldehyde, and preferably formaldehyde, paraformaldehyde or a combi^¬ nation thereof.

In one embodiment of the present invention at least one catalyst is used for the production of the binder composition. In one embodiment of the present invention the catalyst is a base. In one embodiment of the present invention the catalyst is an alkali or an alkali earth hydroxide. In one embodiment of the pre^¬ sent invention the catalyst comprises a salt or a hy^¬ droxide of an alkali metal. In one embodiment of the present invention the catalyst is selected from a group consisting of sodium hydroxide, potassium hydroxide and any mixture thereof. In one embodiment of the present invention the catalyst is an organic amine .

In this specification, unless otherwise stat^¬ ed, the expression "lignin" should be understood as lignin originating from any suitable lignin source. The lignin may include essentially pure lignin. By the expression "essentially pure lignin" should be under^¬ stood as at least 90 % pure lignin, preferably at least 95 % pure lignin. In one embodiment of the pre^¬ sent invention the essentially pure lignin comprises at most 10 %, preferably at most 5 %, of other compo^¬ nents. Extractives and carbohydrates such as hemicel- luloses can be mentioned as examples of such other components. In one embodiment of the present invention the lignin contains less than 10 weight-%, preferably less than 6 weight-%, and more preferably less than 4 weight-% of carbohydrates. The amount of carbohydrates present in lignin can be measured by high performance anion exchange chromatography with pulsed amperometric detector (HPAE-PAD) in accordance with standard SCAN- CM 71.

In one embodiment of the present invention the ash percentage of lignin is less than 7.5 weight- %, preferably less than 5 weight-%, and more prefera^¬ bly less than 3 weight-%. The ash content can be de^¬ termined by carbonifying and quickly burning a lignin sample so that alkali salts are not melted before the organic matter has been burned (e.g. 20-200°C for 30 minutes, after which temperature is adjusted to 200- 600°C for 1 h, and thereafter adjusting the temperature to 600-700°C for 1 hour), and finally the lignin sample is ignited at 700°C for lh. Ash content of a lignin sample refers to the mass that remains of the sample after burning and ignition, and it is presented as per cent of the sample's dry content.

In one embodiment of the present invention the lignin is selected from a group consisting of kraft lignin, steam explosion lignin, biorefinery lignin, supercritical separation lignin, hydrolysis lignin, flash precipitated lignin, biomass originating lignin, lignin from alkaline pulping process, lignin from soda process, lignin from organosolv pulping and combinations thereof. In one embodiment of the present invention the lignin is wood based lignin. The lignin can originate from softwood, hardwood, annual plants or from a combination thereof.

In one embodiment of the present invention the lignin is Kraft lignin. By "kraft lignin" is to be understood in this specification, unless otherwise stated, lignin that originates from kraft black liq^¬ uor. Black liquor is an alkaline aqueous solution of lignin residues, hemicellulose, and inorganic chemi^¬ cals used in a kraft pulping process. The black liquor from the pulping process comprises components origi^¬ nating from different softwood and/or hardwood species in various proportions. Lignin can be separated from the black liquor by different, techniques including e.g. precipitation and filtration. Lignin usually begins precipitating at pH values below 11 - 12. Different pH values can be used in order to precipitate lig^¬ nin fractions with different properties. These lignin fractions differ from each other by molecular weight distribution, e.g. Mw and Mn, polydispersity, hemicel^¬ lulose and extractive contents. The molar mass of lig^¬ nin precipitated at a higher pH value is higher than the molar mass of lignin precipitated at a lower pH value. Further, the molecular weight distribution of lignin fraction precipitated at a lower pH value is wider than of lignin fraction precipitated at a higher pH value. Also the wood species from which the lignin is separated may affect the molecular weight distribu^¬ tion thereof. The precipitated lignin can be purified from inorganic impurities, hemicellulose and wood ex^¬ tractives using acidic washing steps. Further purification can be achieved by filtration.

The use of Kraft lignin can be determined from the produced binder composition based on the sul^¬ phur content of the binder composition. The sulphur content of the produced binder composition can be de^¬ termined by drying a binder composition sample at a temperature of 105 °C, after which SEM-EDS analysis is carried out, whereby one can determine the ratio of elements heavier than sodium. In one embodiment of the present invention the binder composition contains at least 1 weight-% of sulphur, preferably at least 2 weight-% of sulphur, and more preferably at least 5 weight-% of sulphur. In one embodiment of the present invention the binder composition contains 1 - 20 weight-% of sulphur, preferably 2 - 10 weight-% of sulphur .

In one embodiment of the present invention the lignin is flash precipitated lignin. The term "flash precipitated lignin" should be understood in this specification as lignin that has been precipitat^¬ ed from black liquor in a continuous process by de^¬ creasing the pH of a black liquor flow, under the influence of an over pressure of 200 - 1000 kPa, down to the precipitation level of lignin using a carbon dioxide based acidifying agent, preferably carbon dioxide, and by suddenly releasing the pressure for precipitat^¬ ing lignin. The method for producing flash precipitated lignin is disclosed in patent application FI 20106073. The residence time in the above method is under 300 s. The flash precipitated lignin particles, having a particle diameter of less than 2 ym, form agglomerates, which can be separated from black liquor using e.g. filtration. The advantage of the flash pre^¬ cipitated lignin is its higher reactivity compared to normal kraft lignin. The flash precipitated lignin can be purified and/or activated if needed for the further processing .

In one embodiment of the present invention the lignin is separated from pure biomass. The separa^¬ tion process can begin with liquidizing the biomass with strong alkali followed by a neutralization process. After the alkali treatment the lignin can be precipitated in a similar manner as presented above. In one embodiment of the present invention the separa^¬ tion of lignin from biomass comprises a step of enzyme treatment. The enzyme treatment modifies the lignin to be extracted from biomass. Lignin separated from pure biomass is sulphur-free.

In one embodiment of the present invention the lignin is steam explosion lignin. Steam explosion is a pulping and extraction technique that can be ap^¬ plied to wood and other fibrous organic material.

By "biorefinery lignin" is to be understood in this specification, unless otherwise stated, lignin that can be recovered from a refining facility or pro^¬ cess where biomass is converted into fuel, chemicals and other materials.

By "supercritical separation lignin" is to be understood in this specification, unless otherwise stated, lignin that can be recovered from biomass us^¬ ing supercritical fluid separation or extraction technique. Supercritical conditions correspond to the tem^¬ perature and pressure above the critical point for a given substance. In supercritical conditions, distinct liquid and gas phases do not exist. Supercritical wa- ter or liquid extraction is a method of decomposing and converting biomass into cellulosic sugar by em^¬ ploying water or liquid under supercritical condi^¬ tions. The water or liquid, acting as a solvent, ex^¬ tracts sugars from cellulose plant matter and lignin remains as a solid particle.

In one embodiment of the present invention the lignin is hydrolysis lignin. Hydrolysed lignin can be recovered from paper-pulp or wood-chemical process^¬ es .

In one embodiment of the present invention the lignin originates from an organosolv process. Or- ganosolv is a pulping technique that uses an organic solvent to solubilize lignin and hemicellulose .

In one embodiment of the present invention at least 30 weight-%, and preferably at least 50 weight- is , of the polymerizable substance originates from lig^¬ nin. In one embodiment of the present invention 20 - 100 weight-%; 30 - 80 weight-%; or 40 - 60 weight-%, of the polymerizable substance originates from lignin. At least part of the synthetic polymerizable sub^¬ stance, e.g. phenol, usually used for producing a binder composition, e.g. a phenol-formaldehyde resin, can be replaced with lignin, which is a bio-based ma^¬ terial .

In one embodiment of the present invention preferably at least 55 %, and more preferably at least 65 %, of the molecules in the binder composition have a molecular weight of above 3000 Da.

In one embodiment of the present invention, at most 85 %, and preferably at most 80 %, of the mol^¬ ecules in the binder composition have a molecular weight of above 3000 Da.

In one embodiment of the present invention preferably at least 7 %, more preferably 10 - 25, and even more preferably 13 - 18 %, of the molecules in the binder composition have a molecular weight of below 1000 Da.

In one embodiment of the present invention at least 50 % of the molecules in the binder composition have a molecular weight of above 3500 Da, and more preferably above 4000 Da.

In one embodiment of the present invention at least 15 % of the molecules in the binder composition have a molecular weight of below 2000 Da, and prefera^¬ bly below 1500 Da.

In one embodiment of the present invention at least 35 %, preferably at least 40 %, and more prefer^¬ ably at least 50 %, of the molecules in the binder composition have a molecular weight of above 5000 Da.

In one embodiment of the present invention at least 15, preferably at least 25 %, and more prefera^¬ bly at least 35 %, of the molecules in the binder com^¬ position have a molecular weight of above 10000 Da.

In one embodiment of the present invention, at least 5 %, and preferably at least 10 %, of the molecules in the binder composition have a molecular weight of above 30000 Da.

In one embodiment of the present invention, at most 40 %, and preferably at most 30 %, of the mol^¬ ecules in the binder composition have a molecular weight of above 30000 Da.

In one embodiment of the present invention, at most 70 weight-%, and preferably at most 60 weight- is , of the molecules in the binder composition have a molecular weight of above 10000 Da.

The molecular weight and the molecular weight distribution can be determined by size-exclusion- chromatography (SEC) (Dionex) .

The inventors of the present invention sur^¬ prisingly found out that a binder composition having a certain amount of molecules with a high molecular weight and a certain amount of molecules with a low molecular weight, advantageously affects the proper^¬ ties of the binder composition. The inventors found out that the when using this kind of binder composi^¬ tion for binding together at least two veneers, the molecules with the higher molecular weight will remain in the seam or the glue line while the molecules with lower molecular weight will penetrate into the wooden veneer and the molecules with the lowest molecular weight will penetrate to its cell wall structure thus strengthening the part of the veneer next to the glue- line, the glue-line itself, and the plywood. The part of the veneer next to the glue-line becomes a part of the net structure connected to the glue-line. The binder composition according to the present invention may thus aids in the formation of mechanical inter^¬ locking beneficially affecting the adhesion of the veneers .

The molecules with higher molecular weight advantageously remain in e.g. cracks or scratches on the surface of the veneer, on the surface of which the binder composition is applied, and thus strengthen these possible deficiencies on the surface of the ve^¬ neer. As the molecules in the binder composition with higher molecular weight also remain in the glue-lines between veneers compared to being absorbed by the wood material, the plywood production process will become more flexible in view of operation time used for glu^¬ ing together the veneers. The molecules in the binder composition with lower molecular weight will be absorbed into the wood material and strengthen the sur^¬ face of the wood as such. Thanks to the advantageous molecular weight distribution of the binder composition according to the present invention, the part of the veneer next to the glue-line is strengthened. In addition, the glue-line itself is strengthened. An ad^¬ vantage of the binder composition according to the present invention is that its advantageous properties will remain even if there is some variation in the plywood production process and the production condi^¬ tions thereof.

The polydispersity index of the binder compo^¬ sition according to the present invention is 6 or higher. In one embodiment of the present invention the polydispersity index of the binder composition is preferably above 7, more preferably above 9, and even more preferably above 10. In one embodiment of the present invention the polydispersity index of the binder composition is 6 - 30, and preferably 8 - 20. In one embodiment of the present invention the poly^¬ dispersity index of the binder composition is prefera^¬ bly below 30, more preferably below 25, and even more preferably below 20. The rather high polydispersity index of the used binder composition ensures that mo^¬ lecular weight distribution of the binder composition is rather flat and that essentially no large distinct molecular weight peaks are seen.

In one embodiment of the present invention the gelling time of the binder composition is 2 - 8 minutes, preferably 5 - 7.5 minutes, and more prefera^¬ bly 5.5 - 7 minutes, as measured at a temperature of 130 °C . The gelling time can be determined by adding 0.5 ml of a sample to be tested in a test tube with a rod. The sample shall not be stirred. The test tube is then heated to 130 °C in a glycerin or oil bath without mixing. The time until the sample becomes pasty (melted solid) is measured after which the measurement is completed.

In principle, cross-laminated plywood con^¬ sists of three or more layers of veneer sheets, each glued with its grain at right angle to adjacent layers (cross-bonding or cross-lamination) . Laminated veneer lumber (LVL) is another wood product that consists of multiple layers of thin wood assembled with adhesives. The main difference between cross-laminated plywood and laminated veneer lumber is that LVL is strongly orientated because of parallel grain orientation of veneer sheets throughout the structure, whereas cross- laminated plywood is cross-bonded or cross-laminated with alternating grain orientations throughout the structure. I.e. laminated veneer lumber consists of layers of wood veneers laminated together with the grain of each veneer parallel primarily to the length of the finished product. The production of cross- laminated plywood enables to produce plywood with in^¬ creased strength both in longitudinal direction and transverse direction. In general the cross-lamination may have an adverse effect to the plywood production process as the process is not continuous. For example the open time from glue spreading to pressing is different between the veneers for the plywood and plywood panels .

The cross-laminated plywood may comprise e.g. from three veneers up to dozens of veneers.

In one embodiment of the present invention, the cross-laminated plywood comprises a plurality of veneers with at most 55 %, preferably at most 35 %, and most preferably at most 10 %, of the glue-lines therein being situated directly between veneers with parallel grain direction.

In one embodiment of the present invention the cross-laminated plywood comprises at least 5, preferably at least 10, and more preferably at least 15 veneers.

In one embodiment of the present invention the cross-laminated plywood comprises a plurality of veneers with only one glue-line, on both sides of which the grain direction of the veneers is the same.

In one embodiment of the present invention the cross-laminated plywood comprises an uneven number of veneers with no glue-line, on both sides of which the grain direction of the veneers is the same. The so-called open time in the plywood pro^¬ duction process is typically 5 - 30 min but the open time may be even longer. An advantage of the binder composition according to the present invention is that it is beneficial when used for cross-bonded veneers where the open time varies. The binder composition ac^¬ cording to the present invention has the advantage of having a combination of molecules with low, medium and high molecular weights. The molecules with a low mo^¬ lecular weight have surface wetting properties and the ability to penetrate into the veneers and to prevent dry outs, whereas high molecular weight molecules give better prepress tack and open time tolerance. However, molecules, with a high molecular weight, are not able to penetrate into the veneers, but mainly remain in the glue line. The advantage of the combination of molecules with different molecular weights is that over-flowing or over-penetration of the binder composition as well as drying of the binder composition at a too early stage is decreased or prevented even if the open time varies. The binder composition according to the present invention has the advantage of having a good prepress tack after prepress. This is beneficial for the following process stages, such as the hot press stage.

Even if there is variation in the open time during the plywood production process, it is possible to have a glue-line with high strength properties when the binder composition according to the present invention is used. This is important with cross-laminated plywood because the cross-lamination gives high strength properties for the longitudinal and the transverse direction of the plywood. Cross-lamination together with the binder composition according to the present invention results in plywood with high strength properties in the whole structure and espe^¬ cially in the glue lines. In one embodiment of the present invention, at least the other of the outmost veneers of the ply^¬ wood is cross-laminated in relation to its adjacent veneer, and preferably both of the outmost veneers of the plywood are cross-laminated in relation to their respective adjacent veneers.

The embodiments of the invention described hereinbefore may be used in any combination with each other. Several of the embodiments may be combined to^¬ gether to form a further embodiment of the invention. A method, a cross-laminated plywood, a composition or a use, to which the invention is related, may comprise at least one of the embodiments of the invention de^¬ scribed hereinbefore.

An advantage of the present invention is that a cross-laminated plywood production method enabling a broad operating window to be used is achieved with the use of a binder composition according to the present invention. An advantage of the present invention is that a lower hot pressing temperature can be used in the cross-laminated plywood production process.

An advantage of the present invention is that a bio-based binder composition with properties espe^¬ cially suitable for cross-laminated plywood production can be formed.

An advantage of the present invention is that the strength of the cross-laminated plywood produced by the method according to the present invention is increased as the binder composition partly penetrates into the wood material and partly remains in the glue line .

EXAMPLES

Reference will now be made in detail to the embodiments of the present invention, an example of which is illustrated in the accompanying drawing. The description below discloses some embodi^¬ ments of the invention in such a detail that a person skilled in the art is able to utilize the invention based on the disclosure. Not all steps of the embodi^¬ ments are discussed in detail, as many of the steps will be obvious for the person skilled in the art based on this specification.

EXAMPLE 1 - Preparing a binder composition and the use thereof for producing cross-laminated plywood.

In this example a lignin-phenol-formaldehyde binder composition was produced.

The following procedure was applied. Firstly, a synthetic phenol-formaldehyde binder composition was produced by polymerizing phenol and formaldehyde in the presence of water and sodium hydroxide (NaOH) as a catalyst. Formaldehyde was added in a stepwise manner to an aqueous phenol composition and thereafter the temperature of the formed composition was increased up to 80 - 90 °C . The composition was cooked at this tem^¬ perature until a viscosity value of 270 cP was reached. The viscosity was measured at 25 °C using a rotary viscometer (e.g. Brookfield) . To this composi^¬ tion, lignin was physically mixed. I.e. the lignin was not polymerized with the phenol-formaldehyde composi^¬ tion. The lignin used was lignin separated from hard^¬ wood and softwood, and had an average molar mass of 5000 g/mol. The amounts of the different compounds used may vary and are obvious for a person skilled in the art .

The molecular weight distribution of the formed binder composition was determined by size- exclusion chromatography. The polydispersity index (PDI) was determined by size-exclusion chromatography. The polydispersity index (PDI) is a measure of the distribution of molecular mass in a given polymer sam- pie. The PDI is calculated as the weight average mo^¬ lecular weight divided by the number average molecular weight. PDI indicates the distribution of individual molecular masses in a batch of polymers. The properties of the formed binder composition are indicated in the below table:

The binder composition formed as above indi^¬ cated was thereafter used for the production of different kinds of cross-laminated plywood. The following veneers were used for the cross-laminated plywood pro^¬ duction :

The density values were measured in the exam^¬ ples in this specification in accordance with stand^¬ ards SFS-EN 384 and ISO 3131.

The formed binder composition was applied on the surface of the veneers and the wood veneers were joined together by the binder composition. The wood veneers with the binder composition were pressed by hot-pressing technique. The plywood hot-pressing temperature used was about 130°C. The pressure used var^¬ ied depending on the wood species used. For determining the optimum hot-pressing time needed for the different plywood, the temperature rise of the innermost glue line of the plywood panel was followed. The hot- pressing time was the time it took to reach 100°C, plus two minutes for curing the binder composition. The binder composition of the present invention was found suitable for gluing the tested wood veneers to^¬ gether and thus for manufacturing cross-laminated ply^¬ wood. The bonding met the requirements of the standard EN 314-2 (class 1 and class 3) (SFS-EN 314-2. Plywood. Bonding quality. Part 2: Requirements. (1993)).

EXAMPLE 2 - Preparing a binder composition and the use thereof for producing cross-laminated plywood.

In this example a lignin-phenol-formaldehyde binder composition was produced. The binder composi^¬ tion was formed following in a similar kind of proce^¬ dure as presented in Example 11 below. The main dif^¬ ferences between Example 2 and Example 11 are higher molar ratio of NaOH/phenol and the type of lignin used. The binder composition was produced under alka^¬ line conditions. The lignin used in this example was Kraft lignin from softwood with an average molar mass of about 8000 g/mol. The weight ratio of lignin/phenol was 1 : 1

The viscosity of the binder composition was 442 cP. The molecular weight distribution of the formed binder composition was determined by size- exclusion chromatography. The polydispersity index was determined by size-exclusion-chromatography . The properties of the formed binder composition are indicated in the below table: Binder composition of Ex-

Property

amp1e 2

Percentage of the mole^¬ cules having a molecular 72

weight of above 3000 Da

Percentage of the mole^¬ cules having a molecular 13

weight of below 1000 Da

Percentage of the mole^¬ cules having a molecular 52

weight of above 5000 Da

Percentage of the mole^¬ cules having a molecular 42

weight of above 10000 Da

Polydispersity index 13

The formed binder composition was applied on the surface of the veneers and the wood veneers were joined together by the binder composition in a manner discussed above for Example 1. The binder composition of the present invention was found suitable for gluing the tested wood veneers together and thus for manufac^¬ turing cross-laminated plywood. The bonding met the requirements of the standard EN 314-2 (class 1 and class 3) (SFS-EN 314-2. Plywood. Bonding quality. Part 2: Requirements. (1993)).

COMPARATIVE EXAMPLE 3 - Preparing a binder composition and the use thereof for producing cross-laminated ply^¬ wood In this comparative example a phenol- formaldehyde binder composition was produced.

The synthetic phenol formaldehyde binder com^¬ position was produced by polymerizing phenol and formaldehyde in the presence of sodium hydroxide (NaOH) cL S cL C3.talyst. The binder composition was produced un^¬ der alkaline conditions with a surplus of formalde^¬ hyde. The molar ratio of the formaldehyde/phenol/NaOH was 2.1:1:0.7.

Formaldehyde was added in a stepwise manner to an aqueous phenol composition and thereafter the temperature of the formed composition was increased up to 80 - 90 °C . The composition was cooked at this tem^¬ perature until a viscosity value of 270 cP was reached. The viscosity was measured at 25 °C using a rotary viscometer.

The molecular weight distribution of the formed binder composition was determined by size- exclusion chromatography. The polydispersity index was determined by size-exclusion chromatography. The properties of the formed binder composition are indicated in the below table:

Binder composition of

Property

Comparative example 3

Percentage of the mole^¬ cules having a molecular 50

weight of above 3000 Da

Percentage of the mole^¬ cules having a molecular 23

weight of below 1000 Da

Percentage of the mole^¬ cules having a molecular 39

weight of above 5000 Da

Percentage of the mole^¬ cules having a molecular 13

weight of above 10000 Da

Polydispersity index 5 The binder composition formed as above indi^¬ cated was thereafter used for the production of different kinds of cross-laminated plywood. The following veneers were used for the cross-laminated plywood pro^¬ duction :

The formed binder composition was applied on the surface of the veneers and the wood veneers were joined together by the binder composition in a manner discussed above for Example 1.

EXAMPLES 4 - 10 - Preparing a binder composition and the use thereof for producing cross-laminated plywood

Further binder compositions were prepared in accordance with the procedure as presented in Example 2. The replacement level of lignin to phenol used in the examples was the following:

The molecular weight distribution of the formed binder compositions were determined by size- exclusion chromatography. The polydispersity indexes were determined by size-exclusion chromatography. The properties of the formed binder compositions are indi^¬ cated in the below table.

The binder compositions 4 - 10 formed as above indicated were thereafter used for the produc^¬ tion of different kinds of cross-laminated plywood. The following veneers were used for the cross- laminated plywood production:

The formed binder composition was applied on the surface of the veneers and the wood veneers were joined together by the binder composition in a manner discussed above for Example 1. The binder compositions of the present invention were found suitable for glu- ing the tested wood veneers together and thus for man^¬ ufacturing cross-laminated plywood. The bonding met the requirements of the standard EN 314-2 (class 1 and class 3) (SFS-EN 314-2. Plywood. Bonding quality. Part 2: Requirements. (1993)).

EXAMPLE 11 - Preparing a binder composition and the use thereof for producing cross-laminated plywood.

In this example a lignin-phenol-formaldehyde binder composition was produced.

The lignin used in this example was Kraft lignin from softwood and hardwood with an average mo^¬ lar mass of about 5000 g/mol. The molar ratio of for- maldehyde/polymerizable substance (phenol and lig^¬ nin) /NaOH was 1.9:1:0.7., and weight ratio of lig- nin/phenol was 1:1.

Firstly, lignin was added to a composition comprising NaOH and water while heating the composition. Thereafter phenol was added after which part of the formaldehyde was added. The rest of the formalde^¬ hyde was added in a stepwise manner by heating the composition at a temperature of 73 - 78 °C . NaOH was then added to the composition and then the composition was heated at a temperature of 83 - 90 °C for almost three hours. Then the composition was cooled. The vis^¬ cosity of the binder composition was 310 cP.

The molecular weight distribution of the formed binder composition was determined by size- exclusion chromatography. The polydispersity index was determined by size-exclusion-chromatography . The properties of the formed binder composition are indicated in the below table:

Binder composition of Ex-

Property

amp1e 2

Percentage of the mole^¬

75

cules having a molecular weight of above 3000 Da

Percentage of the mole^¬ cules having a molecular 9

weight of below 1000 Da

Percentage of the mole^¬ cules having a molecular 65

weight of above 5000 Da

Percentage of the mole^¬ cules having a molecular 40

weight of above 10000 Da

Polydispersity index 10

The formed binder compositions were subjected to different measurements and tests. The following measurements were carried out: 1) Mechanical hardening of the binder compo^¬ sitions were measured via Automatic Bonding Evaluation System (ABES) . ABES technique involves measuring the shear strength developed between two thin overlapping, parallel in grain veneer strips to which binder composition has been applied. The binder composition is cured under controlled conditions of temperature, pressure and pressing time, and then, immediately af^¬ ter bonding, the lap-shear bond strength is measured with an integrated unit. The bonds are not cooled pri^¬ or to strength testing.

Small birch veneer specimens with size of 0.8 x 20 x 117 mm were cut from the conditioned veneer sheets. Liquid binder compositions from Comparative Example 3 and Example 2, respectively, were applied to one veneer surface to give a binder composition spread rate of 100 g/m². The open assembly time was 0 min, hot-pressing pressure was 2.0 MPa and platen tempera^¬ ture was 105 °C or 130 °C. The failure force was meas^¬ ured after 20, 40, 60, 90, 120 and 160 s.

The results from the measurements are pre^¬ sented in Fig. 2. The results showed that the binder composition of Example 2, where the lignin replacement was 50 %, reached faster the adequate failure force especially at lower temperatures. This is a beneficial feature in hot-press time optimization.

The open assembly time tolerance or operating window of the two binder compositions was evaluated by using ABES technique. Again, small birch veneer speci^¬ mens with size of 0.8 x 20 x 117 mm were cut from the conditioned veneer sheets. Liquid binder composition from Comparative Example 3 or Example 2, respectively, was applied to one veneer surface to give a resin spread rate of 100 g/m². Hot-pressing pressure was 2.0 MPa and platen temperature was 130 °C. The open assem^¬ bly time varied between 0 and 60 minutes. The results from the measurements are pre^¬ sented in Fig. 3, wherein Y-axis indicates percent^¬ ages. 80 % is a sufficient value for the glue-line. The results show that the binder composition according to Example 2 reached the final glue line shear strength level faster than the binder composition according to Comparative Example 3 (10 minutes vs. 20 minutes) . In addition, this reached level could be kept as far as 60 minutes. Thus, the operating window of the lignin based binder composition is wider than with currently used binder compositions (Comparative Example 3) .

2) Chemical hardening of binder compositions was measured by Differential Scanning Calorimetry (DSC) . Dynamic and isothermal measurement runs were used. Measurements were done in sealed cold cells un^¬ der oxygen atmosphere. The binder composition sample size was approximately 5 mg. Firstly, isothermal DSC measurement was performed at 105°C. Secondly, to ana^¬ lyse the post-hardening or amount of unreacted resins, a dynamic DSC measurements from 30 °C up to 250°C at a rate of 10 °C/min were performed.

The results from the measurements are pre^¬ sented in Fig. 1. The results show that 80 % of binder composition according to Example 2 has been cured after 5.7 minutes, while it takes 11.5 minutes for the binder composition according to Comparative Example 3 to reach the same level of curing. The heat of reac^¬ tion (J/g) during post-curing was at the same level with both binder compositions, i.e. there was no sig^¬ nificant difference in the amount of unreacted binder composition. The lignin based binder composition (Example 2) cure faster than binder composition without the lignin (Comparative Example 3) , especially at low^¬ er temperatures.

3) The gelling time of different binder com^¬ positions were determined. The gelling time was deter- mined by adding 0.5 ml of a sample to be tested in a test tube with a rod. The sample was not to be stirred. The test tube was then heated to 130 °C in a glycerin or oil bath without mixing. The time until the sample became pasty (melted solid) was measured after which the measurement was completed.

The measurement was carried out for the bind^¬ er compositions according to Comparative Example 3, Example 2, Example 4 and Example 9, respectively. The results are indicated in the below table.

Table. Results from the gelling time measurements

From the above table it can be seen that the gelling time is decreased when using the lignin containing binder compositions according to the present invention .

4) Mill trial was carried out with the binder composition according to Example 11. The binder composition according to Example 11 was used to produce a plywood glue with a target viscosity of 40-50 s (FC6) according to SFS-EN ISO 2431 (Paints and varnishes - Determination of flow time by use of flow cups. (2011)) after 2 hours. The adhesive was produced with the following:

The adhesive formulation was used to produce 9-ply birch plywood panels in mill scale. The spread^¬ ing rate of the adhesive formulation was about 165 g/m². Panels were pre-pressed for 8 minutes at 1.0 MPa and then hot-pressed for 11 minutes at 130°C and 1.7 MPa. The open time varied between 10 to 30 minutes. Bond quality from 16 panels (originated from 8 lay ups, 16 panels per each) was measured according to EN 314 after soaking and boiling pre-treatments. The re^¬ sults are presented in the below table.

A corresponding test was carried out using the binder composition according to Comparative Example 3. The results received are presented in the below table .

In the binder production method presented in the examples above, phenol and formaldehyde are used. However, other polymerizable substance or crosslinking agent can be equally well used in the binder composi^¬ tion production method as will be obvious for the skilled person based on this specification. Also other wood veneers than birch veneers or spruce veneers can be equally well used for the production of cross- laminated plywood as will be obvious for the skilled person based on this specification.

It is obvious to a person skilled in the art that with the advancement of technology, the basic idea of the invention may be implemented in various ways. The invention and its embodiments are thus not limited to the examples described above; instead they may vary within the scope of the claims.

Claims

1. A method for producing cross-laminated plywood, c h a r a c t e r i z e d in that the method comprises applying an aqueous binder composition on at least one surface of at least one veneer, wherein the aqueous binder composition is prepared by using at least polymerizable substance and crosslinking agent, and wherein:

- at least 20 weight-% of the polymerizable substance originates from lignin;

- the polydispersity index of the binder com^¬ position is 6 or higher.

2. The method of claim 1, wherein at least two veneers are glued together with the binder compo^¬ sition.

3. The method of any one of claims 1 - 2, wherein at least two veneers are glued together with the binder composition under the influence of hot pressing .

4. The method of any one of claims 1 - 3, wherein the density of the wood material of the veneer is 320 - 750 kg/m³, and preferably 390 - 650 kg/m³.

5. The method of any one of claims 1 - 3, wherein the density of the wood material of the veneer is 390 - 550 kg/m³ or 520 - 650 kg/m³.

6. The method of any one of claims 1 - 3, wherein the density of the wood material of the veneer is 450 - 570 kg/m³.

7. The method of any one of claims 1 - 6, wherein the veneer is selected from a group consisting of pine veneer, poplar veneer, beech veneer, aspen veneer, spruce veneer, and birch veneer.

8. The method of any one of claims 1 - 6, wherein the veneer is birch veneer.

9. The method of any one of claims 1 - 6, wherein the veneer is softwood veneer, and preferably spruce veneer or pine veneer.

10. The method of any one of claims 1 - 9, wherein at least one veneer is manufactured by rotary cutting .

11. The method of any one of claims 1 - 10, wherein the thickness of the at least one veneer is 0.5 - 4 mm, preferably 1 - 3.5 mm, and more preferably 1.3 - 3.0 mm .

12. The method of any one of claims 1 - 11, wherein at least 20 % of the veneers of the cross- laminated plywood has a thickness which is at least 0.2 mm, and preferably at least 0.5 mm, less or more than the thickness of the rest of the veneers in the cross-laminated plywood.

13. The method of any one of claims 1 - 11, wherein all the veneers of the cross-laminated plywood are equally thick, with the precision of 0.2 mm

14. The method of any one of claims 1 - 13, wherein the average moisture percentage of the veneers to be used for producing cross-laminated plywood be^¬ fore applying the binder composition thereon is 1 - 9, and preferably 2 - 6.

15. The method of any one of claims 1 - 14, wherein at least one veneer is modified by heat treat^¬ ment, chemical treatment, mechanical treatment, or by a combination thereof.

16. The method of any one of claims 1 - 15, wherein at least one veneer is modified by chemical treatment .

17. The method of any one of claims 1 - 16, wherein the polymerizable substance comprises lignin and at least one of phenol, cresol, and resorcinol.

18. The method of any one of claims 1 - 17, wherein the crosslinking agent is an aldehyde, and preferably formaldehyde, paraformaldehyde or a combi^¬ nation thereof.

19. The method of any one of claims 1 - 18, wherein the lignin is Kraft lignin.

20. The method of any one of claims 1 - 19, wherein at least 30 weight-%, and preferably at least 50 weight-%, of the polymerizable substance originates from lignin.

21. The method of any one of claims 1 - 19, wherein 20 - 100 weight-%; 30 - 80 weight-%; or 40 - 60 weight-%, of the polymerizable substance originates from lignin.

22. The method of any one of claims 1 - 21, wherein preferably at least 55 %, and more preferably at least 65 %, of the molecules in the binder composi^¬ tion have a molecular weight of above 3000 Da.

23. The method of any one of claims 1 - 22, wherein at most 85 %, and preferably at most 80 %, of the molecules in the binder composition have a molecu^¬ lar weight of above 3000 Da.

24. The method of any one of claims 1 - 23, wherein preferably at least 7 %, more preferably 10 - 25 %, and even more preferably 13 - 18 %, of the mole^¬ cules in the binder composition have a molecular weight of below 1000 Da.

25. The method of any one of claims 1 - 24, wherein at least 50 % of the molecules in the binder composition have a molecular weight of above 3500 Da, and preferably above 4000 Da.

26. The method of any one of claims 1 - 25, wherein at least 15 % of the molecules in the binder composition have a molecular weight of below 2000 Da, and preferably below 1500 Da.

27. The method of any one of claims 1 - 26, wherein at least 35, preferably at least 40 %, and more preferably at least 50 %, of the molecules in the binder composition have a molecular weight of above 5000 Da.

28. The method of any one of claims 1 - 27, wherein at least 15, preferably at least 25 %, and more preferably at least 35 %, of the molecules in the binder composition have a molecular weight of above 10000 Da.

29. The method of any one of claims 1 - 28, wherein at least 5 %, and preferably at least 10 %, of the molecules in the binder composition have a molecu^¬ lar weight of above 30000 Da.

30. The method of any one of claim 1 - 29, wherein at most 40 %, and preferably at most 30 %, of the molecules in the binder composition have a molecu^¬ lar weight of above 30000 Da.

31. The method of any one of claims 1 - 30, wherein at most 70 weight-%, and preferably at most 60 weight-%, of the molecules in the binder composition have a molecular weight of above 10000 Da.

32. The method of any one of claims 1 - 31, wherein the polydispersity index of the binder compo^¬ sition is preferably above 7, more preferably above 9, and even more preferably above 10.

33. The method of any one of claims 1 - 32, wherein the polydispersity index of the binder compo^¬ sition is preferably below 30, more preferably below 25, and even more preferably below 20.

34. The method of any one of claims 1 - 33, wherein the polydispersity index of the binder compo^¬ sition is 6 - 30, and preferably 8 - 20.

35. The method of any one of claims 1 - 34, wherein the gelling time of the binder composition is 2 - 8 minutes, preferably 5 - 7.5 minutes and more preferably 5.5 - 7 minutes, as measured at a tempera^¬ ture of 130 °C.

36. Cross-laminated plywood comprising at least two veneers glued together with an aqueous bind^¬ er composition, which is prepared by using at least polymerizable substance and crosslinking agent, and wherein :

- at least 20 weight-% of the polymerizable substance originates from lignin;

- the polydispersity index of the binder com^¬ position is 6 or higher.

37. The cross-laminated plywood of claim 36, wherein the cross-laminated plywood comprises a plu^¬ rality of veneers with at most 55 %, preferably at most 35 %, and most preferably at most 10 %, of the glue-lines therein being situated directly between ve^¬ neers with parallel grain direction.

38. The cross-laminated plywood of claim 36, wherein the cross-laminated plywood comprises a plu^¬ rality of veneers with only one glue-line, on both sides of which the grain direction of the veneers is the same.

39. The cross-laminated plywood of claim 36, wherein the cross-laminated plywood comprises an une^¬ ven number of veneers with no glue-line, on both sides of which the grain direction of the veneers is the same .

40. The cross-laminated plywood of any one of claims 36 - 39, wherein the cross-laminated plywood comprises at least 10, and preferably at least 15 ve^¬ neers .

41. The cross-laminated plywood of any one of claims 36 - 40, wherein at least the other of the out^¬ most veneers of the plywood is cross-laminated in re- lation to its adjacent veneer, and preferably both of the outmost veneers of the plywood are cross-laminated in relation to their respective adjacent veneers.

42. The cross-laminated plywood of any one of claims 36 - 41, wherein the polymerizable substance comprises lignin and at least one of phenol, cresol, and resorcinol.

43. The cross-laminated plywood of any one of claims 36 - 42, wherein the crosslinking agent is an aldehyde, and preferably formaldehyde, paraformalde^¬ hyde or a combination thereof.

44. The cross-laminated plywood of any one of claims 36 - 43, wherein the lignin is Kraft lignin.

45. The cross-laminated plywood of any one of claims 36 -44, wherein at least 30 weight-%, and pref^¬ erably at least 50 weight-%, of the polymerizable sub^¬ stance originates from lignin.

46. The cross-laminated plywood of any one of claims 36 - 44, wherein 20 - 100 weight-%; 30 - 80 weight-%; or 40 - 60 weight-%, of the polymerizable substance originates from lignin.

47. The cross-laminated plywood of any one of claims 36 - 46, wherein preferably at least 55 %, and more preferably at least 65 %, of the molecules in the binder composition have a molecular weight of above 3000 Da.

48. The cross-laminated plywood of any one of claims 36 - 47, wherein at most 85 %, and preferably at most 80 %, of the molecules in the binder comspoti- ion have a molecular weight of above 3000 Da.

49. The cross-laminated plywood of any one of claims 36 - 48, wherein preferably at least 7 ~6 , more preferably 10 - 25 %, and even more preferably 13 - 18 %, of the molecules in the binder composition have a molecular weight of below 1000 Da.

50. The cross-laminated plywood of any one of claims 36 - 49, wherein at least 50 % of the molecules in the binder composition have a molecular weight of above 3500 Da, and preferably above 4000 Da.

51. The cross-laminated plywood of any one of claims 36 - 50, wherein at least 15 % of the molecules in the binder composition have a molecular weight of below 2000 Da, and preferably below 1500 Da.

52. The cross-laminated plywood of any one of claims 36 - 51, wherein at least 35 %, preferably at least 40 %, and more preferably at least 50 %, of the molecules in the binder composition have a molecular weight of above 5000 Da.

53. The cross-laminated plywood of any one of claims 36 - 51, wherein at least 15 %, preferably at least 25 %, and more preferably at least 35 %, of the molecules in the binder composition have a molecular weight of above 10000 Da.

54. The cross-laminated plywood of any one of claims 36 - 52, wherein at least 5 %, and preferably at least 10 %, of the molecules in the binder composi^¬ tion have a molecular weight of above 30000 Da.

55. The cross-laminated plywood of any one of claims 36 - 54, wherein at most 40 %, and preferably at most 30 %, of the molecules in the binder composi^¬ tion have a molecular weight of above 30000 Da.

56. The cross-laminated plywood of any one of claims 36 - 55, wherein at most 70 weight-%, and pref^¬ erably at most 60 weight-%, of the molecules in the binder composition have a molecular weight of below 10000 Da.

57. The cross-laminated plywood of any one of claims 36 - 56, wherein the polydispersity index of the binder composition is preferably above 7, more preferably above 9, and even more preferably above 10.

58. The cross-laminated plywood of any one of claims 36 - 57, wherein the polydispersity index of the binder composition is preferably below 30, more preferably below 25, and even more preferably below 20.

59. The cross-laminated plywood of any one of claims 36 - 58, wherein the polydispersity index of the binder composition is 6 - 30, and preferably 8 - 20.

60. The cross-laminated plywood of any one of claims 36 - 59, wherein the gelling time of the binder composition is 2 - 8 minutes, preferably 5 - 7.5 minutes and more preferably 5.5 - 7 minutes, as meas^¬ ured at a temperature of 130 °C .

61. An aqueous binder composition, which is prepared by using at least polymerizable substance and crosslinking agent, c h a r a c t e r i z e d in that:

- at least 20 weight-% of the polymerizable substance originates from lignin;

- the polydispersity index of the binder com^¬ position is 6 or higher.

62. The binder composition of claim 61, wherein the polymerizable substance comprises lignin and at least one of phenol, cresol, and resorcinol.

63. The binder composition of any one of claims 61 - 62, wherein the crosslinking agent is an aldehyde, and preferably formaldehyde, paraformalde^¬ hyde or a combination thereof.

64. The binder composition of any one of claims 61 - 63, wherein the lignin is Kraft lignin.

65. The binder composition of any one of claims 61 - 64, wherein at least 30 weight-%, and preferably at least 50 weight-%, of the polymerizable substance originates from lignin.

66. The binder composition of any one of claims 61 - 65, wherein 20 - 100 weight-%; 30 - 80 weight-%; or 40 - 60 weight-%, of the polymerizable substance originates from lignin.

67. The binder composition of any one of claims 61 - 66, wherein preferably at least 55 %, and more preferably at least 65 %, of the molecules in the binder composition have a molecular weight of above 3000 Da.

68. The binder composition of any one of claims 61 - 67, wherein at most 85 %, and preferably at most 80 %, of the molecules in the binder composi^¬ tion have a molecular weight of above 3000 Da.

69. The binder composition of any one of claims 61 - 68, wherein preferably at least 7 ~6 , more preferably 10 - 25 %, and even more preferably 13 - 18 %, of the molecules in the binder composition have a molecular weight of below 1000 Da.

70. The binder composition of any one of claims 61 - 69, wherein at least 50 % of the molecules in the binder composition have a molecular weight of above 3500 Da, and preferably above 4000 Da.

71. The binder composition of any one of claims 61 - 70, wherein at least 15 % of the molecules in the binder composition have a molecular weight of below 2000 Da, and preferably below 1500 Da.

72. The binder composition of any one of claims 61 - 71, wherein at least 35 %, preferably at least 40 %, and more preferably at least 50 %, of the molecules in the binder composition have a molecular weight of above 5000 Da.

73. The binder composition of any one of claims 61 - 72, wherein at least 15 %, preferably at least 25 %, and more preferably at least 35 %, of the molecules in the binder composition have a molecular weight of above 10000 Da.

74. The binder composition of any one of claims 61 - 73, wherein at least 5 %, and preferably at least 10 %, of the molecules in the binder composi^¬ tion have a molecular weight of above 30000 Da.

75. The binder composition of any one of claims 61 - 74, wherein at most 40 %, and preferably at most 30 %, of the molecules in the binder composi^¬ tion have a molecular weight of above 30000 Da.

76. The binder composition of any one of claims 61 - 75, wherein at most 70 weight-%, and pref^¬ erably at most 60 weight-%, of the molecules in the binder composition have a molecular weight of above 10000 Da.

77. The binder composition of any one of claims 61 - 76, wherein the polydispersity index of the binder composition is preferably above 7, more preferably above 9, and even more preferably above 10.

78. The binder composition of any one of claims 61 - 77, wherein the polydispersity index of the binder composition is preferably below 30, more preferably below 25, and even more preferably below 20.

79. The binder composition of any one of claims 61 - 78, wherein the polydispersity index of the binder composition is 6 - 30, and preferably 8 - 20.

80. The binder composition of any one of claims 61 - 79, wherein the gelling time of the binder composition is 2 - 8 minutes, preferably 5 - 7.5 minutes, and more preferably 5.5 - 7 minutes, as meas^¬ ured at a temperature of 130 °C .

81. Use of the binder composition of any one of claims 61 - 80 for producing cross-laminated ply^¬ wood .

82. Use of the binder composition of any one of claims 61 - 80 for gluing together at least two ve^¬ neers .