Patent Application
20200190274
The present invention relates to laminates and a process for their production.
Laminates, for example high pressure laminates, comprise a core of cellulosic fibrous based material and a protective overlay. A decorative layer, generally a paper layer, which may have a solid colour, pattern or decoration is generally provided between the core and the protective overlay, especially when a transparent or translucent overlay is used. The core generally comprises one or more layers of paper, typically kraft paper, impregnated with a thermosetting resin. The decorative layer and/or protective overlay may also be impregnated with a thermosetting resin. During manufacture the layers (core material, decorative layer and overlay) are pressed together under simultaneous application of heat and high pressure to obtain a homogeneous preferably non porous material.
Laminates may be used to provide a surface finish to a substrate for interior or exterior applications, for example walls, partitions, ceilings, doors, flooring, stairs, furniture, trims, windows sills, tables, work tops, counter tops, vanity units, cubicles, balconies, facades and signs. When adapted for exterior use the laminate may comprise an additional outer layer or coating to enhance weathering and/or light protecting properties.
Traditionally the thermosetting resin of the core has been a phenol-formaldehyde resin and the thermosetting resin of the surface layer has been a melamine-formaldehyde resin. Whilst such resins provide a number of suitable properties there has for some time been a desire to move away or reduce the use of formaldehyde, particularly for environmental impact. One aim of the present invention is thus to provide a way of producing a low or reduced formaldehyde laminate in a way that provides acceptable properties and is compatible with existing manufacturing methods.
According to one aspect, the present invention provides a method of manufacturing a laminate as defined in claim 1. Addition aspects are defined in other independent claims. The dependent claims define preferred or alternative embodiments.
The term “laminate, as used herein means laminates of the type described above. The laminates may be high pressure laminates (HPL), continuous pressure laminates (CPL), low pressure laminates (LPL) or compact laminates.
One problem associated with the manufacture of laminates is to ensure adequate permeation of a binder, notably in to a core layer. The layer(s) of the laminate must be permeated with a sufficient quantity of binder to provide required strength and resistance when curing in a time frame which allows efficient manufacture, preferably using existing machinery and processes. It has been found that these requirement are met when using the method defined herein.
The term “core binder solution” as used herein means a binder solution used for or adapted for use in the core of a laminate and the term core binder means the binder of the core of a laminate.
The core binder solution may be a binder solution as described in any of WO 2007/014236, WO 2009/019232, WO 2009/019235, WO 2011/138458, WO 2011/138459 or WO 2013/150123 each of which is hereby incorporated by reference.
The core binder solution is preferably “substantially formaldehyde free”, that is to say that it liberates less than 5 ppm formaldehyde as a result of drying and/or curing (or appropriate tests simulating drying and/or curing); it is preferably “formaldehyde free”, that is to say that it liberates less than 1 ppm formaldehyde in such conditions.
The reducing sugar reactant(s) may comprise one or more reducing sugars; it may comprise one or more reducing sugars generated in situ, notably from a carbohydrate reactant which yields reducing sugar(s) in situ, for example due to application of heat and/or presence of a catalyst or further reactant. The nitrogen-containing reactant(s) of the core binder solution are adapted to react with the reducing sugar(s) to form a binder and/or to form binder precursors.
The aqueous core binder solution may comprises: (a) unreacted reducing sugar reactant(s) and unreacted nitrogen-containing reactant(s); or (b) reaction product(s) of reducing sugar reactant(s) and nitrogen-containing reactant(s); or (c) a combination of (a) and (b).
The nitrogen-containing reactant(s) and the reducing sugar reactant(s) (or their reaction product(s)) may be Maillard reactants that react to form Maillard reaction products, notably melanoidins when cured. Curing of the binder may comprise or consists essentially of Maillard reaction(s). The cured binder may comprise melanoidin-containing and/or nitrogenous-containing polymer(s); it is preferably a thermoset binder and is preferably substantially water insoluble.
Solutions containing reaction product(s) of nitrogen containing reactant(s) and reducing sugar reactant(s) prior to curing (notably prior to crosslinking by application of heat and or pressure) may comprise intermediate reaction specie(s), for example pre-polymers, in significant quantities, and/or reduced viscosity per solid content and/or increased average molecular weight, and/or increased colour and/or light (eg UV) absorption.
The reducing sugar reactant may comprise: a monosaccharide, a monosaccharide in its aldose or ketose form, a disaccharide, a polysaccharide, a triose, a tetrose, a pentose, xylose, an hexose, dextrose, fructose, a heptose, a sugar, molasses, starch, starch hydrolysate, cellulose hydrolysates, reaction product(s) thereof or mixtures thereof. The reducing sugar reactant may have a dextrose equivalent of at least about 50, at least about 60, at least about 70, at least about 80 or at least about 90.
The nitrogen-containing reactant may comprise ammonia, NH3, inorganic amine(s), organic amine(s) comprising at least one primary amine group, salts thereof and combinations thereof. For example, the nitrogen-containing reactant may comprise NH3 (e.g. in the form of an aqueous solution), any type of inorganic and organic ammonium salts, ammonium sulfate, ammonium phosphate, ammonium chloride, ammonium nitrate and combinations thereof. The nitrogen-containing reactant may comprise a polyamine; it may comprise a primary polyamine. Herein, the term “polyamine” includes any organic compound having two or more amine groups, which may independently be substituted. As used herein, a “primary polyamine” is an organic compound having two or more primary amine groups (—NH2). Within the scope of the term primary polyamine are those compounds which can be modified in situ or isomerize to generate a compound having two or more primary amine groups (—NH2). The primary polyamine may be a diamine, for example a di-primary diamine, triamine, tetraamine, or pentamine. The polyamine may comprise a diamine selected from 1,2-diaminoethane, 1,4-diaminobutane, 1,5-diaminopentane, 1,6-diaminohexane (hexamethylenediamine, HMDA), 1,12-diaminododecane, 1,4-diaminocyclohexane, 1,4-diaminobenzene, 1,5-diamino-2-methylpentane (2-methyl-pentamethylenediamine), 1,3-pentanediamine, and 1,8-diaminooctane. The nitrogen-containing reactant may comprise a primary polyamine polyether-polyamine; said polyether-polyamine may be a diamine or a triamine.
The reducing sugar reactant(s), may make up:
The nitrogen-containing reactant(s) may make up:
The aqueous core binder solution may comprises (i) at least 25%, and preferably at least 40%, at least 50% or at least 60% by dry weight of: (a) reducing sugar reactant(s) and nitrogen-containing reactant(s) and/or (b) curable reaction product(s) of reducing sugar reactant(s) and nitrogen-containing reactant(s).
The core binder may include ester and/or polyester compounds.
The non-aqueous solvent is a solvent other than water; it should be miscible with water. It may comprise a polar protic solvents, for example an alcohol, notably methanol, ethanol, butanol, propanol or isopropanol, diethanolamine. A preferred solvent comprises or consists of methanol. The non-aqueous solvent may comprise a polar aprotic solvent, for example acetonitrile, dimethylformamide, dimethyl sulfoxide, tetrahydrofuran, acetone, dichloromethane or ethyl acetate. Combinations of any two or more solvents may also be used.
The non-aqueous solvent may be present in the uncured aqueous binder solution in a quantity of:
The uncured aqueous binder solution, notably in the state in which it is impregnated into the core material may have a viscosity which is:
The uncured aqueous binder solution may have a solid content of:
The core material comprises one or more fibrous layers, notably of any suitable fibrous sheet materials, for example cellulosic fibrous sheet material, which can be saturated with, or can absorb the uncured aqueous core binder solution. Preferably the core material comprises one or more fibrous paper sheet materials, for example of kraft paper. The kraft paper may have a weight which is ≥80 g/m2 or ≥100 g/m2 and/or ≤300 g/m2 or ≤200 g/m2, for example about 105 g/m2.
The binder of the surface layer is preferably a thermosetting binder and may comprise an amino-formaldehyde resin, preferably a urea-formaldehyde, melamine-formaldehyde, etherified urea-formaldehyde or etherified melamine-formaldehyde or phenolic formaldehyde, acrylic-, epoxy-, polyester-, or polyurethane- resins or combinations thereof. In a preferred embodiment it comprises melamine binder.
The binder of the surface layer may be or comprise the same binder as the core binder.
Particularly for a high pressure laminate , applying heat and pressure to the semi-finished assembly may comprise applying a pressure which is ≥60 kg/cm2 (≥ about 850 lb per sq inch) or ≥70 kg/cm2 (≥ about 1000 lb per sq inch) or ≥84 kg/cm2 (≥ about 1200 lb per sq inch) and/or ≤140 kg/cm2 (≤ about 2000 lb per sq inch) or ≤120 kg/cm2 (≤ about 1700 lb per sq inch) or ≤100 kg/cm2 (≤ about 1420 lb per sq inch). The core binder and the binder of the surface layer are preferably cured at the same time in a single curing step; nevertheless, they may be cured separately.
Pressing conditions, notably for a high pressure laminate may include use a press, for example a multi-daylight press, to produce a number of laminates per cycle which is greater than or equal to 5, 10 or 20 and/or less than or equal to 600, 500, 400, 300 or 200. The preferred thickness of each of the laminates with theses pressing conditions is greater than or equal to 0.5 mm, 1 mm or 2 mm and/or less than or equal to 50 mm, 40 mm, 30 mm or 20 mm. The temperature of the press may be greater than or equal to about 100° C. or 120° C. and/or less than or equal to about 160° C. or 150° C. The presstime (i.e. duration from entry in to the press to exit from the press) may be:
Pressing conditions, notably for a short cycle high pressure laminate, may include use of a single-daylight press to press one or two laminates per cycle. The preferred thickness for the laminates with theses pressing conditions may be greater than or equal to 0.5 mm, 1 mm or 2 mm and/or less than or equal to 20 mm, 18 mm or 15 mm. The temperature of the press may be greater than or equal to about 140° C. or 160° C. and/or less than or equal to about 220° C. or 200° C. The presstime may be:
Particularly for continuous pressure laminates , applying heat and pressure to the semi-finished assembly may comprise applying a pressure which is ≥20 kg/cm2 (≥ about 285 lb per sq inch) or ≥25 kg/cm2 (≥ about 355 lb per sq inch) or ≥30 kg/cm2 (≥ about 425 lb per sq inch) and/or ≤80 kg/cm2 (≤ about 1135 lb per sq inch) or ≤75 kg/cm2 (≤ about 1065 lb per sq inch) or 70 kg/cm2 (≤ about 1000 lb per sq inch).
Pressing conditions, notably for continuous pressure laminates, may use a double-belt press. The preferred thickness for the laminates with these pressing conditions is greater than or equal to 0.1 mm, 0.2 mm or 0.3 mm and/or less than or equal to 1.5 mm or 1.2 mm. The temperature of the press may be greater than or equal to about 140° C. or 160° C. and/or less than or equal to about 220° C. or 200° C. The presstime may be:
Particularly for low pressure laminates, pressing conditions may include a temperature of the press greater than or equal to about 140° C. or 160° C. and/or less than or equal to about 220° C. or 200° C. Applying heat and pressure to the semi-finished assembly may comprise applying a pressure which is ≥15 kg/cm2 or ≥20 kg/cm2 and/or ≤40 kg/cm2 or ≤50 kg/cm2 for example about 30 kg/cm2 (about 430 lb per sq inch). The presstime may be:
The laminate may comprise a number of layers in the core layer which is ≥2, ≥3, ≥5, ≥10, ≥20, ≥30, ≥40 or ≥50 and/or ≤250, ≤200, ≤180, ≤150 or ≤100.
The invention will be illustrated with reference to the non-limiting examples set out in Table 1.
The permeation time and viscosity of the binders of Examples 1-10 shown in Table 1 was assessed and compared against a comparative example of a phenol formaldehyde based binder which is not in accordance with the present invention using the following test protocol:
Examples 3, 6, 9 and 10 in particular show an average permeation time (and thus an ability to impregnate laminate core material) which is comparable with, and indeed better than, the standard phenol formaldehyde resin of the comparative example.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1413402.7 | Jul 2014 | GB | national |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15329875 | Jan 2017 | US |
| Child | 16798254 | US |
