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GB2196342A - Manufacture of fibreboard - Google Patents

Manufacture of fibreboard Download PDF

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Publication number
GB2196342A
GB2196342A GB08724097A GB8724097A GB2196342A GB 2196342 A GB2196342 A GB 2196342A GB 08724097 A GB08724097 A GB 08724097A GB 8724097 A GB8724097 A GB 8724097A GB 2196342 A GB2196342 A GB 2196342A
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GB
United Kingdom
Prior art keywords
urea
formaldehyde
resin
solution
weight
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.)
Granted
Application number
GB08724097A
Other versions
GB2196342B (en
GB8724097D0 (en
Inventor
Brian Vyse
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Borden
Hexion Inc
Original Assignee
Borden
Borden Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Borden, Borden Inc filed Critical Borden
Publication of GB8724097D0 publication Critical patent/GB8724097D0/en
Publication of GB2196342A publication Critical patent/GB2196342A/en
Application granted granted Critical
Publication of GB2196342B publication Critical patent/GB2196342B/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/20Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08L61/22Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
    • C08L61/24Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with urea or thiourea
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27NMANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
    • B27N1/00Pretreatment of moulding material
    • B27N1/003Pretreatment of moulding material for reducing formaldehyde gas emission
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L97/00Compositions of lignin-containing materials
    • C08L97/02Lignocellulosic material, e.g. wood, straw or bagasse

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Forests & Forestry (AREA)
  • Dry Formation Of Fiberboard And The Like (AREA)
  • Reinforced Plastic Materials (AREA)

Abstract

A cellulose fibre composite is manufactured by a method comprising blending together a urea- formaldehyde pre-polymer resin having a high formaldehyde:urea mole ratio, a particulate cellulose fibre material and a urea solution. The blend is then subjected to hot pressing to give fibreboard with low free formaldehyde content yet good physical strength.

Description

SPECIFICATION Manufacture of fibreboard The present invention relates to the manufacture of cellulose fibre-based composites, e.g. particleboard and medium density fibreboard, using urea-formaldehyde resins as binders.
In the production of such compositions using urea-formaldehyde resin binders, the small amounts of formaldehyde retained in the board after manufacture can cause environmental problems at some later date. It is therefore desirable to minimise this free formaldehyde content as much as possible without sacrificing the advantages that are achieved from the use of ureaformaldehyde resin binders. Many ways of solving the problem have been proposed and the approach most commonly used in the industry is to reduce the formaldehyde:urea mole ratio in the resin. Although this solves the particular problem of free formaldehyde in the product, it unfortunately causes reduced reactivity, reduced bonding efficiency and reduced storage stability of the resin.Reduced bonding efficiency in the product is displayed as reduced physical strengths in the board and as increased swelling of the board on being immersed in water or on being subjected to conditions of high humidity.
The present invention is based on the discovery that the above problems of the prior art can be avoided by the addition of a urea solution to the urea-formaldehyde resin binder prior to the hot pressing stage of the resin/fibre mixture. Accordingly, the present invention provides a method of manufacturing a cellulose fibre composite comprising blending together a urea-formaldehyde pre-polymer resin having a high formaldehyde: urea mole ratio, a particulate cellulose fibre material and a urea solution, and subjecting the mixture obtained to hot pressing.
Typically the particulate cellulose fibre material used in the present invention will comprise any of the materials conventionally used in the manufacture of cellulose fibre composites. In particular, we have achieved good results using wood chips and medium density wood fibres. The use of a high formaldehyde ratio resin blended simultaneously with urea solution and wood fibres has been found to give the following advantages over the use of a resin of equivalent final molar ratio: (a) improved storage life of resin pre-polymer compared with conventionally used resins; (b) lower formaldehyde emission for finished board; (c) improved tensile strengths perpendicular to the plane of the board (i.e. known as "internal bond").
The urea-formaldehyde pre-polymer resins useful in the present invention have a high formaldehyde:urea mole ratio. By "high formaldehyde:mole ratio" we mean a formaldehyde:urea mole ratio of not less than 1.8:1. Typically, the urea:formaldehyde prepolymer resin used in the present invention will have a molar ratio of formaldehyde:urea of from 1.8 to 3.5:1 and preferably about 2.5:1. The pre-polymer resin will generally have a pH value in the range of 6.5 to 9.0 in order that it has good storage stability. Preferably, the pH of the pre-polymer resin will have a value in the range of from 7.0 to 8.0. The solids content and the viscosity of the prepolymer resin are not critical to the working of the present invention.However, the pre-polymer resin will generally have a solids content of from 55 to 70% by weight and a viscosity in the range of from 500 to 5000 cP at 25"C.
According to the present invention urea, as an aqueous solution, is added to the high formaldehyde resin in an amount sufficient to give a final formaldehyde: urea molar ratio of typically from 1.1-1.6:1, preferably about 1.2:1. The concentration of urea in the aqueous urea solution is not critical to the working of the invention although in practice it will be adjusted to give a convenient quantity of addition. A 50% (by weight) concentration of urea will normally be convenient. For a 50% urea solution, a typical quantity of addition is from 20 to 50% based on the amount of pre-polymer resin and depending on the mole ratio of the pre-polymer and the final mole ratio required. Other additives, such as wax emulsion conventionally used to improve hydrophobicity, may also be incorporated with the components mentioned above.
In general, the resin will be used in an amount to give a % resin solids (based on the weight of dry fibre) in the range of from 8 to 10%, preferably 6 to 8%.
The method of the invention is particularly suitable for the manufacture of medium density fibre (MDF) board where the resin is added to the wood fibre by "blow line" blending. Preferably the pre-polymer solution, the urea solution and a wax emulsion are metered separately through metering pumps and introduced simultaneously into a static mixer. The mixture is then flowed to the chip blender or, if appropriate, the blow line. In the case of blow line blending, it is also possible to meter the urea components directly into the blow line without the use of a static mixer.
The mixture of prepolymer, particulate cellulose fibre material and urea solution obtained by blending the components together is subjected to hot pressing. Hot pressing techniques are, of course, well known in the art and do not require detailed discussion here. Generally, however, pressing temperatures in the range of from 1500 to 2200C, preferably from 1 7or to 200"C, will be used. The moisture content of the material prior to pressing will usually be in the range of from 7 to 14% and more usually from 9 to 12%. Pressure will be varied throughout the pressing cycle, up to a maximum of about 400 psi, to produce fibreboard of a typical density, of 600-800 Kg/m3, preferably 680-750 Kg/m3.
EXAMPLE I A pre-polymer resin I was prepared by acidifying 20009 of a 50% (by volume) aqueous solution of formaldehyde with a 50% (by volume) sulphuric acid solution to give a pH of 1.8.
This solution was heated to 60"C and 7809 of urea was added slowly allowing temperature to rise to 850C. After neutralising with 32% (by weight) caustic soda solution to a pH of 7.0-7.4 the resin was distilled under vacuum at 60 C to remove 4009 distillate, finally cooling to 25"C or below. This pre-polymer solution had a viscosity of approximately 200cP at 25"C and a solids content after drying for 3 hours at 120"C of 60% by weight and a molar ratio of formaldehyde to urea of 2.55:1.
A resin II was made using the same quantities and process as above but after distillation the resin was cooled to 50"C and a further 8869 urea were added and allowed to react for 1 hour at 40"C prior to cooling to 25"C.
MDF boards were made using blow line mixing of resin and fibre. In the case of pre-polymer I, the flow rates of fibre, pre-polymer I and 50% urea solution were set to give the ratios:fibre 90 parts by weight, pre-polymer 1 10.9 parts by weight, 50% (by weight) urea solution 8.2 parts by weight-equivalent to 10% binder solids on dry fibre. In the case of resin II, the flow rates were set to give the ratios: fibre 90 parts by weight and resin 11 15 parts by weight again giving 10% binder solids on dry fibre. In both cases fibres were dried to 10% moisture content, formed into a mat and hot pressed for 3 minutes at 1700C to give a 12mm thick MDF board of about 750Kg/m3 density.Duplicate boards were tested and the following results obtained: Internal Total Extractable Bond Formaldehyde Density MPa mg/100g Pre-polymer I+urea 760 0.66 3 Pre-polymer l+urea 750 0.61 10 Resin II 750 0.60 20 Resin Il 740 0.52 16 EXAMPLE II A pre-polymer Ill was made by adding 9109 urea to 20009 50% (by volume) formaldehyde solution at a pH of 7.0-7.2, heating for 10 minutes at 100"C, dropping pH to 5-6 and reacting until a viscosity of 80cSt @ 25"C was reached, neutralising to pH 7.0-7.5 and distilling at 60"C to remove 3009 of water.The resulting pre-polymer resin solution had a viscosity of 200cPs @ 20"C and a solids content of 60% by weight. A similar resin was made but after distillation and cooling to 50"C a further 6209 urea was added and reacted at 40"C for one hour before finally cooling to 180cP at 20 C and a solids content of 65% by weight.
MDF boards were made by simultaneously mechanically blending dried wood fibres with prepolymer Ill and a 50% (by weight) urea solution in the ratio:wood fibre 90 parts by weight, prepolymer lit 11 parts by weight and 50% urea solution 8 parts by weight and similar boards were made using wood fibre 90 parts by weight and resin IV 15 parts by weight. In both cases, a total binder content of 10% was used and boards were pressed at 170 C for three minutes. The following results were obtained: Internal Total extractable Density Bond formaldehyde kg/m3 MPa mg/1009 Board made with pre-polymer Ill +urea 760 0.52 48 Board made with resin IV. 740 0.43 77

Claims (7)

1. A method of manufacturing a cellulose fibre composite comprising blending together a urea-formaldehyde pre-polymer resin having a high formaldehyde:urea mole ratio, a particulate cellulose fibre material and a urea solution, and subjecting the mixture obtained to hot pressing.
2. A method according to claim 1, wherein the urea-formaldehyde pre-polymer resin has a formaldehyde:urea molar ratio in the range of from 1.8:1 to 3.5:1.
3. A method according to claim 2, wherein the urea-formaldehyde pre-polymer resin has a formaldehyde: urea molar ratio of about 2.5:1.
4. A method according to any one of claims 1 to 3, wherein the urea solution is added in an amount sufficient to give a final formaldehyde: urea molar ratio in the range of from 1.1:1 to 1.6:1.
5. A method according to claim 4, wherein the urea solution is added in an amount sufficient to give a final formaldehyde: urea molar ratio of about 1.2:1.
6. A method according to any one of claims 1 to 5, wherein the urea solution has a urea concentration of about 50% by weight.
7. A method according to any one of claims 1 to 6, wherein the particulate cellulose fibre material is selected from wood chips and medium density wood fibres.
GB8724097A 1986-10-14 1987-10-14 Manufacture of fibreboard Expired - Lifetime GB2196342B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB868624557A GB8624557D0 (en) 1986-10-14 1986-10-14 Manufacture of fibreboard

Publications (3)

Publication Number Publication Date
GB8724097D0 GB8724097D0 (en) 1987-11-18
GB2196342A true GB2196342A (en) 1988-04-27
GB2196342B GB2196342B (en) 1990-06-27

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Family Applications (2)

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GB868624557A Pending GB8624557D0 (en) 1986-10-14 1986-10-14 Manufacture of fibreboard
GB8724097A Expired - Lifetime GB2196342B (en) 1986-10-14 1987-10-14 Manufacture of fibreboard

Family Applications Before (1)

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GB868624557A Pending GB8624557D0 (en) 1986-10-14 1986-10-14 Manufacture of fibreboard

Country Status (3)

Country Link
ES (1) ES2005034A6 (en)
GB (2) GB8624557D0 (en)
IE (1) IE60045B1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992008588A1 (en) * 1990-11-12 1992-05-29 Derek Worthington Maude Method and apparatus for producing insulation materials
US20180362405A1 (en) * 2015-12-03 2018-12-20 Kyoto University Resin composition and method for producing same

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB979757A (en) * 1962-09-05 1965-01-06 Allied Chem Improvements in or relating to bonding of materials together by means of urea-formaldehyde adhesives
GB1014961A (en) * 1963-07-15 1965-12-31 Ciba Ltd Improvements in or relating to the manufacture of particle boards
GB1228954A (en) * 1967-04-14 1971-04-21
US4175150A (en) * 1976-11-05 1979-11-20 Masonite Corporation Urea containing high density skin fiberboard with a low density core

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2039919B (en) * 1978-07-06 1983-02-09 Akesson A Method of manufacturing bonded products of cellulose or cellulose derivatives

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB979757A (en) * 1962-09-05 1965-01-06 Allied Chem Improvements in or relating to bonding of materials together by means of urea-formaldehyde adhesives
GB1014961A (en) * 1963-07-15 1965-12-31 Ciba Ltd Improvements in or relating to the manufacture of particle boards
GB1228954A (en) * 1967-04-14 1971-04-21
US4175150A (en) * 1976-11-05 1979-11-20 Masonite Corporation Urea containing high density skin fiberboard with a low density core

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
WO 80/00142 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992008588A1 (en) * 1990-11-12 1992-05-29 Derek Worthington Maude Method and apparatus for producing insulation materials
US20180362405A1 (en) * 2015-12-03 2018-12-20 Kyoto University Resin composition and method for producing same

Also Published As

Publication number Publication date
GB2196342B (en) 1990-06-27
IE872747L (en) 1988-04-14
IE60045B1 (en) 1994-05-18
GB8724097D0 (en) 1987-11-18
ES2005034A6 (en) 1989-02-16
GB8624557D0 (en) 1986-11-19

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Legal Events

Date Code Title Description
732E Amendments to the register in respect of changes of name or changes affecting rights (sect. 32/1977)
732E Amendments to the register in respect of changes of name or changes affecting rights (sect. 32/1977)
PCNP Patent ceased through non-payment of renewal fee

Effective date: 20041014