GB1576310A - Composite sheet materials comprising resin-impregnated supporting materials - Google Patents
Composite sheet materials comprising resin-impregnated supporting materials Download PDFInfo
- Publication number
- GB1576310A GB1576310A GB33700/76A GB3370076A GB1576310A GB 1576310 A GB1576310 A GB 1576310A GB 33700/76 A GB33700/76 A GB 33700/76A GB 3370076 A GB3370076 A GB 3370076A GB 1576310 A GB1576310 A GB 1576310A
- Authority
- GB
- United Kingdom
- Prior art keywords
- range
- resin
- liquid composition
- dispersion
- acrylate resin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000463 material Substances 0.000 title claims description 43
- 239000002131 composite material Substances 0.000 title claims description 18
- 238000000034 method Methods 0.000 claims description 68
- 239000004925 Acrylic resin Substances 0.000 claims description 48
- 239000000203 mixture Substances 0.000 claims description 47
- 229920005989 resin Polymers 0.000 claims description 40
- 239000011347 resin Substances 0.000 claims description 40
- 239000006185 dispersion Substances 0.000 claims description 39
- 239000007788 liquid Substances 0.000 claims description 38
- 229920003180 amino resin Polymers 0.000 claims description 31
- 229920000877 Melamine resin Polymers 0.000 claims description 16
- 239000000123 paper Substances 0.000 claims description 16
- 238000003825 pressing Methods 0.000 claims description 15
- 239000000243 solution Substances 0.000 claims description 15
- 239000004640 Melamine resin Substances 0.000 claims description 13
- VQLYBLABXAHUDN-UHFFFAOYSA-N bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane;methyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 VQLYBLABXAHUDN-UHFFFAOYSA-N 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 11
- 239000004094 surface-active agent Substances 0.000 claims description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 7
- 125000000129 anionic group Chemical group 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 6
- 238000005189 flocculation Methods 0.000 claims description 5
- 230000016615 flocculation Effects 0.000 claims description 5
- 238000005259 measurement Methods 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- 229920001169 thermoplastic Polymers 0.000 claims description 4
- 239000004416 thermosoftening plastic Substances 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 239000010425 asbestos Substances 0.000 claims description 2
- 239000011093 chipboard Substances 0.000 claims description 2
- 230000007423 decrease Effects 0.000 claims description 2
- 230000000694 effects Effects 0.000 claims description 2
- 229910052895 riebeckite Inorganic materials 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 4
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 229920001131 Pulp (paper) Polymers 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000004849 latent hardener Substances 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- NJYZCEFQAIUHSD-UHFFFAOYSA-N acetoguanamine Chemical compound CC1=NC(N)=NC(N)=N1 NJYZCEFQAIUHSD-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- -1 as appropriate Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007596 consolidation process Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000003678 scratch resistant effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/37—Polymers of unsaturated acids or derivatives thereof, e.g. polyacrylates
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B21/00—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board
- B32B21/04—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board comprising wood as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B21/06—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board comprising wood as the main or only constituent of a layer, which is next to another layer of the same or of a different material of paper or cardboard
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B13/00—Layered products comprising a a layer of water-setting substance, e.g. concrete, plaster, asbestos cement, or like builders' material
- B32B13/04—Layered products comprising a a layer of water-setting substance, e.g. concrete, plaster, asbestos cement, or like builders' material comprising such water setting substance as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B13/08—Layered products comprising a a layer of water-setting substance, e.g. concrete, plaster, asbestos cement, or like builders' material comprising such water setting substance as the main or only constituent of a layer, which is next to another layer of the same or of a different material of paper or cardboard
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B21/00—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board
- B32B21/02—Layered products comprising a layer of wood, e.g. wood board, veneer, wood particle board the layer being formed of fibres, chips, or particles, e.g. MDF, HDF, OSB, chipboard, particle board, hardboard
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B29/00—Layered products comprising a layer of paper or cardboard
- B32B29/02—Layered products comprising a layer of paper or cardboard next to a fibrous or filamentary layer
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/38—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing crosslinkable groups
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/47—Condensation polymers of aldehydes or ketones
- D21H17/49—Condensation polymers of aldehydes or ketones with compounds containing hydrogen bound to nitrogen
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/47—Condensation polymers of aldehydes or ketones
- D21H17/49—Condensation polymers of aldehydes or ketones with compounds containing hydrogen bound to nitrogen
- D21H17/51—Triazines, e.g. melamine
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2260/00—Layered product comprising an impregnated, embedded, or bonded layer wherein the layer comprises an impregnation, embedding, or binder material
- B32B2260/02—Composition of the impregnated, bonded or embedded layer
- B32B2260/028—Paper layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2260/00—Layered product comprising an impregnated, embedded, or bonded layer wherein the layer comprises an impregnation, embedding, or binder material
- B32B2260/04—Impregnation, embedding, or binder material
- B32B2260/046—Synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2315/00—Other materials containing non-metallic inorganic compounds not provided for in groups B32B2311/00 - B32B2313/04
- B32B2315/12—Asbestos
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2317/00—Animal or vegetable based
- B32B2317/12—Paper, e.g. cardboard
- B32B2317/125—Paper, e.g. cardboard impregnated with thermosetting resin
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
- D21H23/02—Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
- D21H23/22—Addition to the formed paper
- D21H23/32—Addition to the formed paper by contacting paper with an excess of material, e.g. from a reservoir or in a manner necessitating removal of applied excess material from the paper
- D21H23/42—Paper being at least partly surrounded by the material on both sides
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Structural Engineering (AREA)
- Laminated Bodies (AREA)
Description
(54) IMPROVEMENTS IN OR RELATING TO COMPOSITE SHEET MATERIALS
COMPRISING RESIN-IMPREGNATED SUPPORTING MATERIALS
(71) We, HOECHST HOLLAND N.V., a limited liability company of 25, Sara
Burgerhartstraat, Amsterdam, the Netherlands, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement:
This invention relates to the preparation of composite sheet materials by consolidating an assembly of a supporting sheet and one or more layers of resin impregnated supporting material, such as paper or analogous material, thereby to improve the surface of the supporting sheet.
In accordance with one aspect of the present invention there is provided a method of preparing a composite sheet material, by consolidating an assembly of a supporting sheet and one or more layers of resin-impregnated supporting material, that is characterised by impregnating paper or analogous supporting material in a single bath with a liquid composition containing an aminoplast resin and an acrylate resin which are compatible with each other, the quantity of acrylate resin with respect to aminoplast resin in the liquid composition being in the range 1 to 9.0% by weight based on the total solids content.
The aminoplast resin and acrylate resin may each conveniently be in the form of a solution, e.g. an aqueous solution, or a dispersion, e.g. an aqueous dispersion. Preferably, an aqueous dispersion with an ionic, e.g. weakly anionic, surface-active substance is used. It is also possible to use dispersions with cationic or non-ionic surface-active substances, provided the composition is such that no flocculation occurs.
The constituents of the liquid composition are preferably selected bearing in mind the compatibility of the resins with each other and with the supporting material and the tendency of the resins to flocculate on drying, it being advantageous to use compositions with which no flocculation of the resins occurs on drying. In this connection, it should be noted that, particularly when the aminoplast resin is a malamine resin, these properties depend on the quantity of available water remaining after drying following impregnation. This quantity of water determines to a great extent the properties of the impregnated material prior to and during pressure to form a composite sheet, as will be discussed below, and hence affects the surface properties of the resulting product.
Thus, in one preferred embodiment the liquid composition comprises a melamine resin and an acrylate resin which is compatible with paper, the composition being such that no flocculation of the resins occurs on drying.
In another preferred embodiment of the invention, the liquid composition comprises an aqueous dispersion of an aminoplast and a solution of an acrylate resin.
The liquid composition may also comprise, for example, a dispersion of an acrylate resin in a solution of aminoplast resin, e.g. melamine resin. In this case, the properties of the resulting product are affected by the surface charge of the dispersion, the particle size and the ionic character of the aminoplast resin solution and any modifying agents, and these may be appropriately selected to give a product having suitable properties.
Preferably an aqueous dispersion with an ionic surface-active substance is used. In this case, the desired ionic character of the dispersion may be obtained by using appropriate mixtures of anionic and non-ionic surface-active substances during the preparation of the acrylate resin. Such dispersions result in the production of impregnated material with a surface that is smooth, highly lustrous and has appropriate optical properties.
It is found particularly advantageous to use a dispersion of an acrylate resin in which the dispersion has a viscosity in the range 20 to 45 cPs and a pH in the range 5 to 7, the acrylate resin having a hardness in the range 0.5 to 5 x 1010 dynes/cm2 at OOC and a particle size in the range 0.01 to 0.35 microns. It should, however, be noted that acrylate resin solutions are also very suitable.
Further, the liquid composition need not necessarily comprise wholly separate acrylate resin and aminoplast resin solutions or dispersions, and may instead comprise a polycondensate in which acrylate resin is partly condensed with melamine resin.
The aminoplast resin may conveniently comprise a melamine resin, e.g. a melamine/formaldehyde condensate that may be produced in conventional manner, i.e. by subjecting melamine and formaldehyde to condensation in an aqueous alkaline solution. In this case, the mol ratio of melamine to formaldehyde is generally in the range 1:1.5 to 1:3. The melamine in the condensate can be partly or entirely replaced by other amino compounds, such as dicyandiamide, benzoguanamine or acetoguanamine, the mol ratios and reaction conditions being adapted accordingly.
The acrylate resin conveniently comprises copolymers of esters of acrylic acid that are compatible with the aminoplast resin, suitable copolymerisates conveniently being diluted with and dispersed in water.
Preferably, use is made of a netting acrylate resin, that is, a resin that crosslinks upon heating, in order to impart improved chemical and ultraviolet resistance to the resulting impregnated supporting material and composite supporting sheet produced therefrom.
Further, it is found that thermoplastic acrylate resins with a great degree of hardness (measured according to DIN 53445) appear to be very efficient.
Preferably, the quantity of acrylate resin with respect to aminoplast resin in the liquid composition is in the range 3 to 7%by weight based on the total solids content, such quantities producing very good results. More preferably, the liquid composition contains 5 % by weight acrylate resin with respect to aminoplast resin, based on the total solids content.
The supporting material to be impregnated by the method of the invention may conveniently be, for example, phenolic resin impregnated kraft paper.
The impregnation may conveniently be effected with any suitable conventional impregnating apparatus equipped with suitable impregnating and metering systems, and thus avoids the need to use two separate impregnating baths, as is the case with certain known methods for preparing impregnated supporting material in which a layer of paper or paper-like material is, for example, first impregnated with an aminoplast resin, one side of the layer subsequently being impregnated with a copolymer of an ester of acrylic acid.
It is found that the impregnating step that characterises the method of the invention produces impregnated paper or similar material in which surprisingly, the acrylate resin and the aminoplast resin, particularly a melamine resin, are so distributed in the thickness of the material that there is uniform and linear gradation of composition in and on the paper, resulting in advantageous processing and production properties. This result is believed to be connected with the behaviour of the supporting material, which acts to regulate distribution of the acrylate resin and aminoplast resin within the thickness of the supporting material, resulting in the highest acrylate content being at the surface of the impregnated supporting material. This, perhaps, accounts for the fact that it is found that the surface of the impregnated product is smooth and, surprisingly, has the properties of an acrylate resin surface notwithstanding the small amount of acrylate resin in the impregnating composition.
These results compare favourably with impregnated materials produced in certain prior art processes in which the transition from aminoplast resin to acrylate resin in and on supporting material is not homogeneous, an asymmetrically built-up thermoplastic film being produced that has great variations in physical and thermal properties in a direction extending perpendicular to the surface of the supporting material. As a result, the adherence between the acrylate resin film and layer of supporting material is not optimal, with the consequence that the resulting film is liable to corrode or crack when stressed.
The consolidation of an assembly of supporting sheet and one or more layers of the resin-impregnated supporting material may be accomplished by the application of appropriately elevated temperatures and pressures to the assembly. Preferably, the assembly is subjected to appropriately elevated pressure at an appropriately elevated constant temperature to form the composite sheet.
It is found that the method of the invention enables production of a composite sheet with a surface layer that combines the advantageous properties of both the acrylate resin and aminoplast resin. being highly glossy owing to the presence of the acrylate resin, yet scratch resistant and chemically resistant owing to the presence of the aminoplast resin.
The supporting sheets used in the method of the invention may be boards such as chipboard, fibreboard and asbestos board bound by organic or inorganic binding agents, the resin-impregnated supporting material conveniently being film-like.
Composite sheets are preferably manufactured in this way by pressing the assembly, e.g. in a suitable press, at pressures in the range 10 to 30 kg/cmZ at a temperature in the range 1200C to 190"C for a time in the range 20 to 80 seconds, the liquid composition used for impregnating the supporting material being such that the resulting impregnated supporting material hardens under such conditions. More preferably, the combination is pressed at pressures in the range 15 to 25 kg/cm2 at a temperature in the range 1700C to 1900C for a time in the range 30 to 60 seconds,
A suitable latent hardener is conveniently added to the liquid composition or a component thereof, e.g. the aminoplast resin, such that the resulting material will harden in less than 60 seconds at a temperature not exceeding 140"C.
As mentioned above, when preparing a composite sheet by the method of the invention, the assembly is preferably subjected to an appropriately elevated pressure at an appropriately elevated constant temperature. This method thus compares favourably with certain prior art methods of preparing composite sheets in which, in order to obtain glossy surfaces on the resulting products, it was necessary to use a multi-stage pressing operation, a typical such method involving firstly pressing sheets in presses at 1500C for, e.g. 10 minutes at pressures ranging from 20 to 30 kg/cm2, and then subsequently cooling the presses to a temperature ranging from 40"C to 800C for further pressing. It is clear that such a multi-stage pressing operation is inconvenient and results in significant energy losses, disadvantages that are not encountered with the present invention.
The present invention also includes within its scope impregnated supporting materials and composite sheets prepared by the methods of the invention.
The present invention will be further illustrated by the following Examples.
Example I
A melamine resin solution comprising 47% by weight solids was mixed with an aqueous acrylate resin dispersion with a ionic surface-active substance, the dispersion containing 45% by weight solids. The constituents were mixed in such quantities that, calculated on the quantity of total solids, 5 %by weight of solid acrylate resin is present in the resulting mixture.
The pH of this mixture was adjusted to 9.2 by means of a dilute base or a dilute acid, as appropriate, and a latent hardener added so as to produce a liquid composition having a curing time in the range 20 to 50 seconds at a temperature of 140"C.
A paper band was impregnated in a bath of this liquid composition and subsequently dried to a volatile components content of 5.0%, resulting in production of impregnated supporting material in the form of a thermoplastic film.
This film was applied to a fibre sheet and pressed in a press for 30 seconds at a constant temperature on a thin smoothing sheet with a lustre rate of 100.
In this Example, three types of paper were used as supporting materials, so-called unipaper, a type of wood pulp paper; a similar decorative wood pulp paper and non-woven cotton fibre fleece. The lustre rate of the surface of each of the resulting composite sheets was measured and the results are shown in the following Table.
Example II
The procedure of Example I was repeated, except a pressing time of 50 seconds was used.
The lustre rates of the resulting products are shown in the Table.
Similar results are obtained by using a solution of a water-soluble acrylate resin instead of a dispersion.
Example III
The procedure of Example I was repeated, except a pressing time of 80 seconds was used.
The lustre rates of the resulting products are shown in the Table.
Example IV
The procedure of Examples I to III inclusive were repeated, using a liquid composition with an acrylate content of 2%, for pressing times of 30, 50 and 80 seconds. The results of lustre rate measurements at the various pressing times are indicated in the Table under IV-a,
IV-b and IV-c respectively.
Example V
Example I was repeated using a liquid composition containing no acrylate for pressing times of 30, 50 and 80 seconds. The results of lustre rate measurements at the various pressing times are indicated in the Table under V-a, V-b and V-c, and it can be seen that these procedures do not produce composite sheets with satisfactory lustre rates.
Example VI
The procedure according to Example I is repeated, but instead of using a separate acrylate resin dispersion or acrylate resin solution use is made of a polycondensate obtained by adding acrylate resin during the preparation of the melamine resin, so that the acrylate is partly condensed with the melamine resin. Results are equivalent to results of other examples in accordance with the invention.
TABLE
pressing Lustre rate
Example Acrylate time ("long" reflection - measurement K 45 ) (sec) Unipaper decorative non-woven
paper fleece
I 5 30 90 90 85
II 5 50 100 95 90
III 5 80 90 90 90
IV-a 2 30 40 40 40
IV-b 2 50 50 50 45
IV-c 2 80 60 55 55
V-a 0 30 20 20 20
V-b 0 50 30 25 20
V-c 0 80 40 35 25
Note:
When longer pressing times are used the measured lustre rate decreases owing to an increased surface activity of the pressed products.
WHAT WE CLAIM IS:
1. A method of preparing a composite sheet material by consolidating an assembly of a supporting sheet and one or more layers of resin-impregnated supporting material, characterised by impregnating paper or analogous supporting material in a single bath with a liquid composition containing an aminoplast resin and an acrylate resin which are compatible with each other. the quantity of acrylate resin with respect to aminoplast resin in the liquid composition being in the range 1 to 9.0% by weight based on the total solids content.
2. A method according to claim 1, wherein the liquid composition comprises a dispersion of an aminoplast resin.
3. A method according to claim 2, wherein the dispersion is an aqueous dispersion.
4. A method according to claim 2 or 3, wherein the dispersion includes an ionic surfaceactive substance.
5. A method according to claim 4, wherein the dispersion includes a weakly anionic surface-active substance.
6. A method according to claim 1, wherein the liquid composition comprises a solution of an aminoplast resin.
7. A method according to any one of the preceding claims, wherein the aminoplast resin comprises a melamine resin.
8. A method according to any one of the preceding claims, wherein the liquid composition comprises a dispersion of an acrylate resin.
9. A method according to claim 8, wherein said dispersion is an aqueous dispersion.
10. A method according to claim 9, wherein said dispersion includes an ionic surfaceactive substance.
11. A method according to claim 10, wherein said dispersion includes a weakly anionic surface-active substance.
12. A method according to any one of claims 8 to 11, wherein said dispersion has a viscosity in the range 20 to 45 cPs and a pH in the range 5 to 7, the acrylate resin having a hardness in the range 0.5 to 5 x 1010 dynes/ cm2 at 0 C and a particle size in the range 0.01 to 0.35 microns.
13. A method according to any one of claims 1 to 7, wherein the liquid composition comprises a solution of an acrylate resin.
14. A method according to claim 13, wherein said solution is an aqueous solution.
15. A method according to any one of the preceding claims, wherein the liquid composition comprises a melamine resin and an acrylate resin which is compatible with paper, the composition being such that no flocculation of the resins occurs on drying.
16. A method according to any one of the preceding claims, wherein the liquid composition comprises a netting acrylate resin.
17. A method according to any one of the preceding claims, wherein the liquid composi
**WARNING** end of DESC field may overlap start of CLMS **.
Claims (33)
1. A method of preparing a composite sheet material by consolidating an assembly of a supporting sheet and one or more layers of resin-impregnated supporting material, characterised by impregnating paper or analogous supporting material in a single bath with a liquid composition containing an aminoplast resin and an acrylate resin which are compatible with each other. the quantity of acrylate resin with respect to aminoplast resin in the liquid composition being in the range 1 to 9.0% by weight based on the total solids content.
2. A method according to claim 1, wherein the liquid composition comprises a dispersion of an aminoplast resin.
3. A method according to claim 2, wherein the dispersion is an aqueous dispersion.
4. A method according to claim 2 or 3, wherein the dispersion includes an ionic surfaceactive substance.
5. A method according to claim 4, wherein the dispersion includes a weakly anionic surface-active substance.
6. A method according to claim 1, wherein the liquid composition comprises a solution of an aminoplast resin.
7. A method according to any one of the preceding claims, wherein the aminoplast resin comprises a melamine resin.
8. A method according to any one of the preceding claims, wherein the liquid composition comprises a dispersion of an acrylate resin.
9. A method according to claim 8, wherein said dispersion is an aqueous dispersion.
10. A method according to claim 9, wherein said dispersion includes an ionic surfaceactive substance.
11. A method according to claim 10, wherein said dispersion includes a weakly anionic surface-active substance.
12. A method according to any one of claims 8 to 11, wherein said dispersion has a viscosity in the range 20 to 45 cPs and a pH in the range 5 to 7, the acrylate resin having a hardness in the range 0.5 to 5 x 1010 dynes/ cm2 at 0 C and a particle size in the range 0.01 to 0.35 microns.
13. A method according to any one of claims 1 to 7, wherein the liquid composition comprises a solution of an acrylate resin.
14. A method according to claim 13, wherein said solution is an aqueous solution.
15. A method according to any one of the preceding claims, wherein the liquid composition comprises a melamine resin and an acrylate resin which is compatible with paper, the composition being such that no flocculation of the resins occurs on drying.
16. A method according to any one of the preceding claims, wherein the liquid composition comprises a netting acrylate resin.
17. A method according to any one of the preceding claims, wherein the liquid composi
tion contains a thermoplastic acrylate resin.
18. A method according to any one of the preceding claims, wherein the quantity of acrylate resin with respect to aminoplast resin in the liquid composition is in the range 3 to 7% by weight based on the total solids content.
19. A method according to claim 18, wherein the quantity of acrylate resin with respect to aminoplast resin in the liquid composition is 5%by weight based on the total solids content.
20. A method according to any one of the preceding claims, wherein the liquid composition comprises a polycondensate in which acrylate resin is partly condensed with melamine resin.
21. A method according to any one of the preceding claims, wherein the liquid composition is such that the resulting impregnated supporting material hardens when subjected to pressures in the range 10 to 30 kg/cm2 at a temperature in the range 1200C to 1900C for a time in the range 20 to 80 seconds.
22. A method according to claim 21, wherein the liquid composition is such that the resultingimprenated supporting material hardens when subjected to pressures in the range 15 to 25 kg/cm at a temperature in the range 170to 1900C for a time in the range 30 to 60 seconds.
23. A method according to any preceding claim, wherein said assembly is consolidated by being subjected to appropriately elevated pressure at an appropriately elevated constant temperature to form the composite sheet.
24. A method according to claim 23, wherein said assembly is pressed at pressures in the range 10 to 30 kg/cm at a temperature in the range 1200C to 1900C for a time in the range 20 to 80 seconds.
25. A method according to claim 24, wherein said assembly is pressed at pressures in the range 15 to 25 kg/cm2 at a temperature in the range 1700C to 1900C for a time in the range 30 to 60 seconds.
26. A method according to any preceding claim, wherein said supporting sheet comprises chipboard, fibreboard or asbestos board.
27. A method according to claim 1, substantially as described with reference to Example
I.
28. A method according to claim 1, substantially as described with reference to Example
II.
29. A method according to claim 1, substantially as described with reference to Example
III.
30. A method according to claim 1, substantially as described with reference to Example
IV.
31. A method according to claim 1 substantially as described with reference to Example
VI.
32. An impregnated supporting material whenever prepared in the course of the method of any one of the preceding claims.
33. A composite sheet whenever prepared by the method of any one of claims 1 to 31.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL7515106.A NL162155C (en) | 1975-12-24 | 1975-12-24 | METHOD FOR MANUFACTURING AN IMPREGNATED FIBER FLUSH AND METHOD FOR MANUFACTURING A CARRIER PLATE |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1576310A true GB1576310A (en) | 1980-10-08 |
Family
ID=19825097
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB33700/76A Expired GB1576310A (en) | 1975-12-24 | 1976-12-23 | Composite sheet materials comprising resin-impregnated supporting materials |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE849857A (en) |
| DE (1) | DE2657973A1 (en) |
| GB (1) | GB1576310A (en) |
| NL (1) | NL162155C (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2752159A1 (en) * | 1977-11-23 | 1979-06-07 | Basf Ag | AGENT FOR SOAKING FIBERS CONTAINING CELLULOSIC |
| DE2903172A1 (en) * | 1979-01-27 | 1980-08-07 | Roehm Gmbh | METHOD FOR PRODUCING PLASTIC-IMPREGNATED PAPERS, FIBER FLEECE AND THE LIKE |
| AT397634B (en) * | 1991-09-30 | 1994-05-25 | Isovolta | METHOD FOR PRODUCING A DRILL BASE AND A DRILL BASE PRODUCED BY THIS METHOD |
| DE19618681A1 (en) * | 1996-05-09 | 1997-11-13 | Roehm Gmbh | Dispersions for paper impregnation containing water glass and / or dextrin |
| ITMI20082053A1 (en) * | 2008-11-19 | 2010-05-20 | Eclissi Srl | HOT GLUEING OF PRINTS ON MDF PANELS (OR MDF TABLES) THROUGH PRESSES AND ADHESIVES |
-
1975
- 1975-12-24 NL NL7515106.A patent/NL162155C/en not_active IP Right Cessation
-
1976
- 1976-12-21 DE DE19762657973 patent/DE2657973A1/en not_active Withdrawn
- 1976-12-23 GB GB33700/76A patent/GB1576310A/en not_active Expired
- 1976-12-24 BE BE173633A patent/BE849857A/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE2657973A1 (en) | 1977-07-07 |
| BE849857A (en) | 1977-06-24 |
| NL7515106A (en) | 1977-06-28 |
| NL162155C (en) | 1980-04-15 |
| NL162155B (en) | 1979-11-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |