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WO2000046306A1 - Timber process and product - Google Patents

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Publication number
WO2000046306A1
WO2000046306A1 PCT/ZA2000/000019 ZA0000019W WO0046306A1 WO 2000046306 A1 WO2000046306 A1 WO 2000046306A1 ZA 0000019 W ZA0000019 W ZA 0000019W WO 0046306 A1 WO0046306 A1 WO 0046306A1
Authority
WO
WIPO (PCT)
Prior art keywords
binding mixture
mdi
mixture
catalyst
binding
Prior art date
Application number
PCT/ZA2000/000019
Other languages
French (fr)
Inventor
Sydney Maboka
Original Assignee
Sappi Limited
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 Sappi Limited filed Critical Sappi Limited
Priority to AU30086/00A priority Critical patent/AU3008600A/en
Priority to CA002361618A priority patent/CA2361618A1/en
Priority to EP00908809A priority patent/EP1161498A1/en
Publication of WO2000046306A1 publication Critical patent/WO2000046306A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/16Catalysts
    • 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

Definitions

  • This invention relates to a timber process and product. More particularly
  • this invention relates to a process for manufacturing so-called particle
  • chipboard that a urea-formaldehyde resin (hereinafter
  • UF UF
  • binders typically contain approximately 55% to 60% formaldehyde
  • chipboard pressing takes place either in a batch-type (using daylight
  • MDI (hereinafter referred to as "MDI") may be added to the aforementioned MDI
  • binding mixture for use in manufacturing chipboard including
  • polyurethane catalyst(s) may or may not be (a) delayed-action catalyst(s).
  • TTI isocyanate
  • TDI isocyanate
  • the aforementioned mixture(s) may of course include a suitable amount
  • resin may preferably be approximately 50% (in moles) i.e. may be less
  • Suitable amines or amine compounds may be selected from the
  • DMEA 2-dimethyl ethanolamine
  • DABCO di-amino bicyclo-octane
  • DMCHA N,N-dimethyl cyclohexylamine
  • Suitable organometallic tin-based compounds may be selected from the
  • organometallic compounds may include ferric
  • Suitable alkali metal salts may be selected from the following:
  • Air Products, South Africa, and the catalysts may be identified inter alia
  • the amount of MDI When used with one or more of the above catalysts, the amount of MDI
  • BDW (hereinafter referred to as "BDW").
  • additive including an effective amount of MDI and a catalyst, each as
  • a process for manufacturing chipboard including the steps of adding to or using in a binding mixture consisting of urea-formaldehyde
  • polyether polyol which is sold by ICI (Imperial Chemical
  • PPG diol MDI Pre-Polymer is the brand name for

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Materials Engineering (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Dry Formation Of Fiberboard And The Like (AREA)

Abstract

This invention provides a binding mixture for use in manufacturing chipboard, the mixture including an effective amount of methyl di-isocyanate ('MDI') and one or more polyurethane catalyst(s) being selected from the following: (a) one or more amine compound(s) including aliphatic and aromatic tertiary amine derivatives of phenols, esters, ethers, alkenes and/or alcohols; or (b) one or more organometallic compounds of tin, bismuth, zinc, iron, and/or alkali metal salt(s); or (c) suitable mixtures of (a) and (b) above.

Description

TIMBER PROCESS AND PRODUCT
INTRODUCTION
This invention relates to a timber process and product. More particularly
this invention relates to a process for manufacturing so-called particle
board or chipboard, and to a timber product in the form of such particle
board or chipboard when manufactured by or from the aforementioned
process.
BACKGROUND TO THE INVENTION
It is known in the manufacture of particle board or chipboard (hereinafter
referred to as "chipboard") that a urea-formaldehyde resin (hereinafter
referred to as "UF") is used as a binder or adhesive to bond the particles
or chips of wood.
Typically such binders contain approximately 55% to 60% formaldehyde
(in moles) but because of recent awareness of the health problems
associated with the use of formaldehyde, the amount of formaldehyde in
such resins is generally being reduced. Hence the amount of
formaldehyde in the aforementioned resins has been reduced to
approximately 50% or less (in moles). The aforementioned resins need to be cured, and the curing process is
accelerated by heating in a press under pressure i.e. heat is applied by
hot metal platens on both sides of a so-called mat of glued chips. Such
chipboard pressing takes place either in a batch-type (using daylight
presses) or in a continuous process i.e. using continuous (for example
roller) presses.
It is also known in the chipboard industry that methyl di-isocyanate
(hereinafter referred to as "MDI") may be added to the aforementioned
type of resin to hasten the curing process i.e. to effectively increase the
speed of the curing process and hence to reduce the curing time.
However, because of the high cost of MDI and the amount required to
effectively hasten the curing process, the use of MDI is not cost-
effective on an industrial scale.
OBJECTS OF THE INVENTION
It is accordingly a general object of the present invention to provide an
improved binding mixture for chipboard manufacture. It is also an object of the present invention to provide an improved
process in which such improved mixture is used, which is both cost-
effective and which increases the efficiency and rate of curing of the
binding mixture.
It is a further object of the invention that the aforementioned binding
mixture and process will lead to an increase in productivity or production
flowing from shorter curing periods resulting from use of the
aforementioned binding mixture.
SUMMARY OF THE INVENTION
According to one aspect of the present invention, there is provided a
binding mixture for use in manufacturing chipboard, the mixture including
an effective amount of MDI and one or more polyurethane catalyst(s)
being selected from the following:
(a) one or more amine compound(s) including aliphatic and aromatic
tertiary amine derivatives of phenols, esters, ethers, alkenes and/or
alcohols; or
(b) one or more organometallic compound(s) of tin, bismuth, zinc, iron
and/or alkali metal salt(s); or
(c) suitable mixtures of (a) and (b) above. The MDI may or may not be water-emulsifiable, and the or each
polyurethane catalyst(s) may or may not be (a) delayed-action catalyst(s).
To the mixture may be added an effective amount of toluene di-
isocyanate ("TDI") and/or one or more internal wetting and release
agents.
The aforementioned mixture(s) may of course include a suitable amount
of urea-formaldehyde resin which may or may not have suitable
quantities of polyol(s) added thereto.
The amount of formaldehyde in the aforementioned urea-formaldehyde
resin may preferably be approximately 50% (in moles) i.e. may be less
than, equal to, or more than 50% (in moles).
By using a catalyst as aforesaid, the effective amount of MDI required is
reduced relative to the amounts known in the prior art to be sufficient to
hasten the curing process of the mixture.
Suitable amines or amine compounds may be selected from the
following: 2-dimethyl ethanolamine (hereinafter referred to as "DMEA");
di-amino bicyclo-octane (hereinafter referred to as "DABCO"); and
N,N-dimethyl cyclohexylamine (hereinafter referred to as "DMCHA").
Suitable organometallic tin-based compounds may be selected from the
following:
stannous octoate, dibutyl tin dilaurate, dibutyl tin mercaptide, dibutyl tin
thiocarboxylate, and dioctyl tin thiocarboxylate.
Other suitable organometallic compounds may include ferric
acetylacetonate.
Suitable alkali metal salts may be selected from the following:
calcium carbonate, salts of carbonic acid, and salts of acetic acid.
One supplier of the above catalysts (as mixtures or single compounds) is
Air Products, South Africa, and the catalysts may be identified inter alia
by the following trade marks/brands and/or acronyms, respectively:
Figure imgf000008_0001
When used with one or more of the above catalysts, the amount of MDI
required to effect a suitable hastening of the curing process may
preferably be in the range of about 0.1 % to 1 .9% on bone dry wood
(hereinafter referred to as "BDW").
According to another aspect of the present invention, there is provided
an additive for a binding mixture for use in manufacturing chipboard, the
additive including an effective amount of MDI and a catalyst, each as
indicated above, and as otherwise described herein.
According to a further aspect of the present invention, there is provided
a process for manufacturing chipboard, the process including the steps of adding to or using in a binding mixture consisting of urea-formaldehyde
resin, an effective amount of MDI and a catalyst, each catalyst being as
indicated above, or as otherwise herein described, or an additive,
respectively, as herein described, and suitably mixing the binding mixture
with wood particles and/or chips.
DETAILED DESCRIPTION OF THE INVENTION
The invention will now be described in greater detail by way of non-
limiting example(s), with reference to the following:
1 . LABORATORY TESTS
Laboratory tests were carried out by way of reasonable technical trials,
by personnel of the applicant's wholly owned subsidiary namely Sappi
Timber Industries (Proprietary) Limited on wood particles and chips as
used for manufacturing chipboard in the factories of the aforementioned
company.
Using the aforementioned raw materials, binder mixtures of urea-
formaldehyde resin as typically used in the aforementioned company's
production facilities were applied to the aforementioned particle chips. and compared with urea-formaldehyde mixtures including MDI, and
further compared with mixtures of urea-formaldehyde with MDI and
various catalysts as set out above.
The resulting mixtures of particles/chips and binder mixtures were
pressed in a laboratory scale press to simulate plant production
conditions, and curing times were measured. In the binding mixtures
that did not include a catalyst, longer curing times were observed.
Details of the mixtures used and the corresponding results are set out in
Table 1 hereafter:
TABLE 1
Figure imgf000011_0001
Table 1 (Contd)
CATALYSTS
(a) 1.4% (on BDW) MDI modified with 45.8 PPG Triol MDI pre-polymer + 0.1% DABCO TMR 2 catalyst
(b) 1.4% (on BDW) MDI modified with 44.3 PPG Triol MDI pre-polymer + 0.1% (on UF mass) DABCO K 15 catalyst
(c) 1.4% (on BDW) MDI modified with 44.3 PPG Triol MDI pre-polymer + 0.1% (on UFmass) DABCO DC 2 catalyst
(d) 1.2% (on BDW) MDI modified with 42.3 PPG Triol MDI pre-polymer + 0.1% (on UFmass) DMCHA catalyst
(e) (1.2% (on BDW) MDI modified 42.3 with PPG Triol MDI pre-polymer + 0.1% (on UF mass) DABCO R8020 catalyst
CD 1.2% (on BDW) MDI modified with 40.0 PPG Triol MDI pre-polymer + 0.1% (on UF mass) Thorcat catalyst
(g) 1.4% (on BDW) MDI modified with 42.8 Polyethylene glycol MDI pre- polymer + 0.1% (on UF mass) DABCO DC 2 catalyst
(h) 0.5% (on BDW) MDI + 1.1% (on 33.3 UF mass) DMEA catalyst
(0 0.5% (on BDW) water emulsified 33.3 MDI + 1.1% (on UF mass) DMEA catalyst In the aforementioned table, the brand name Daltolac R130 is a brand
name for polyether polyol, which is sold by ICI (Imperial Chemical
Industries). Similarly PPG diol MDI Pre-Polymer is the brand name for
polypropylene glycol diol MDI pre-polymer and PPG triol TDI Pre-Polymer
is the brand name for polypropylene glycol triol TDI pre-polymer.
The curing times for mixtures where typically 0.1 % to 1 .9% MDI and
one or more of the abovementioned catalysts were added (on BDW),
were the shortest.
The results of the above tests indicated that in all cases the binding
mixtures with MDI and one or more catalysts resulted in a shorter curing
period with the same or an increased binding strength.
It was also found that the use of amines as catalysts alone resulted in
the least costly mixture and hence the most cost-effective process(es).
2- PRODUCTION-PLANT TRIALS
The aforementioned tests were repeated by way of reasonable technical
trials, on two different production lines namely one using a single
daylight press and the other using a continuous press. Details of the mixtures used and the corresponding results are set out in Table 2
hereunder:
TABLE 2
Figure imgf000014_0001
The abovementioned production-line tests confirmed the aforementioned
laboratory results, with improvements in or increased curing times of up
to approximately 14 to 24% . The applicant believes that it may be
possible to achieve greater improvements than the aforementioned.
It will therefore be seen from the aforementioned that a considerable
improvement in curing times and hence in productivity may be possible
by using the aforementioned invention. Such improvement also appears
to be cost-effective relative to increased productivity and production on
an industrial scale. Although certain embodiments only of the invention have been described
herein, it will be apparent to any person skilled in the art that other
variations and/or modifications of the invention are possible. Such
variations and/or modifications are therefore to be considered as falling
within the spirit and scope of the invention as claimed hereinafter.

Claims

1 . A binding mixture for use in manufacturing chipboard, the mixture
including an effective amount of methyl di-isocyanate ("MDI") and
one or more polyurethane catalyst(s) being selected from the
following:
(a) one or more amine compound(s) including aliphatic and
aromatic tertiary amine derivatives of phenols, esters,
ethers, alkenes and/or alcohols; or
(b) one or more organometallic compounds of tin, bismuth,
zinc, iron, and/or alkali metal salt(s); or
(c) suitable mixtures of (a) and (b) above.
2. A binding mixture as claimed in claim 1 , wherein the MDI is water-
emulsifiable.
3. A binding mixture as claimed in either claim 1 or claim 2, wherein
the or each polyurethane catalyst(s) is/are (a) delayed-action
catalyst(s).
4. A binding mixture as claimed in any one of the preceding claims,
wherein an effective amount of toluene di-isocyanate ("TDI") is
added to the MDI.
5. A binding mixture as claimed in any one of the preceding claims,
wherein one or more internal wetting and release agents is/are
added to the mixture.
6. A binding mixture as claimed in any one of the preceding claims,
wherein a suitable amount of urea-formaldehyde resin is added.
7. A binding mixture as claimed in claim 6, wherein a suitable
quantity of or more one polyol(s) is/are added.
8. A binding mixture as claimed in either claim 6 or claim 7, wherein
the amount of formaldehyde in the urea-formaldehyde resin may
be approximately 50% (in moles).
9. A binding mixture as claimed in any one of the preceding claims,
wherein the or each suitable amine(s) or amine compound(s) are
selected from the following:
2-dimethyl ethanolamine ("DMEA");
di-amino bicyclo-octane ("DABCO"); and
N,N-dimethyl cyclohexylamine ("DMCHA").
10. A binding mixture as claimed in any one of the preceding claims,
wherein the or each suitable organometallic tin-based compound(s)
is/are selected from the following:
Stannous octoate, dibutyl tin dilaurate, dibutyl tin mercaptide,
dibutyl tin thiocarboxylate, and dioctyl tin thiocarboxylate.
1 1 . A binding mixture as claimed in any one of the preceding claims,
wherein the suitable organometallic compounds include ferric
acetylacetonate.
12. A binding mixture as claimed in any one of the preceding claims,
wherein the suitable alkali metal salts are selected from the
following:
calcium carbonate, salts of carbonic acid, and salts of acetic acid.
13. A binding mixture as claimed in any one of the preceding claims,
wherein the amount of MDI required to effect a suitable hastening
of the curing process is in the range of from about 0.1 % to 1 .9%
of bone dry wood ("BDW").
14. A binding mixture substantially as herein described and/or
exemplified.
15. An additive for a binding mixture for use in manufacturing
chipboard, the additive including an effective amount of MDI and a
catalyst, each catalyst being as claimed in any one of the
preceding claims.
16. An additive for a binding mixture for use in making chipboard,
substantially as herein described and/or exemplified.
17. A process for manufacturing chipboard, the process including the
steps of adding to or using in a binding mixture an effective
amount of MDI and a catalyst, each catalyst being as claimed in
any one of claims 1 to 14, and suitably mixing the binding mixture
with wood particles and/or chips.
18. A process for manufacturing chipboard, the process including the
steps of adding to or using in a binding mixture an effective
amount of an additive as claimed in either claim 15 or claim 16,
and suitably mixing the binding mixture with wood particles and/or
chips.
19. A process for manufacturing chipboard, substantially as herein
described and/or exemplified.
PCT/ZA2000/000019 1999-02-08 2000-02-08 Timber process and product WO2000046306A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
AU30086/00A AU3008600A (en) 1999-02-08 2000-02-08 Timber process and product
CA002361618A CA2361618A1 (en) 1999-02-08 2000-02-08 Timber process and product
EP00908809A EP1161498A1 (en) 1999-02-08 2000-02-08 Timber process and product

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ZA99/0969 1999-02-08
ZA99969 1999-02-08

Publications (1)

Publication Number Publication Date
WO2000046306A1 true WO2000046306A1 (en) 2000-08-10

Family

ID=25587553

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/ZA2000/000019 WO2000046306A1 (en) 1999-02-08 2000-02-08 Timber process and product

Country Status (4)

Country Link
EP (1) EP1161498A1 (en)
AU (1) AU3008600A (en)
CA (1) CA2361618A1 (en)
WO (1) WO2000046306A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10142296C1 (en) * 2001-08-29 2003-02-13 Bayer Ag Polyurethane elastomers, used for making moldings, e.g. shoe soles, are produced using an amine catalyst and a catalyst mixture of organic titanium and/or zirconium and lithium compounds in reaction of isocyanate and polyether polyol
WO2004113428A1 (en) * 2003-06-24 2004-12-29 Agro Biomass Consult Aps Method for mixing and homogenisation of binding agents and additives

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0039137A1 (en) * 1980-04-30 1981-11-04 Imperial Chemical Industries Plc Isocyanate reactions
EP0346059A2 (en) * 1988-06-07 1989-12-13 Btg International Limited Composite materials
US5002713A (en) * 1989-12-22 1991-03-26 Board Of Control Of Michigan Technological University Method for compression molding articles from lignocellulosic materials
WO1992009645A1 (en) * 1990-11-27 1992-06-11 Weyerhaeuser Company Isocyanate modified cellulose products and method for their manufacture
WO1994005475A1 (en) * 1992-09-03 1994-03-17 Glunz Ag Process for manufacturing fibre or particle boards

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0039137A1 (en) * 1980-04-30 1981-11-04 Imperial Chemical Industries Plc Isocyanate reactions
EP0346059A2 (en) * 1988-06-07 1989-12-13 Btg International Limited Composite materials
US5002713A (en) * 1989-12-22 1991-03-26 Board Of Control Of Michigan Technological University Method for compression molding articles from lignocellulosic materials
WO1992009645A1 (en) * 1990-11-27 1992-06-11 Weyerhaeuser Company Isocyanate modified cellulose products and method for their manufacture
WO1994005475A1 (en) * 1992-09-03 1994-03-17 Glunz Ag Process for manufacturing fibre or particle boards

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10142296C1 (en) * 2001-08-29 2003-02-13 Bayer Ag Polyurethane elastomers, used for making moldings, e.g. shoe soles, are produced using an amine catalyst and a catalyst mixture of organic titanium and/or zirconium and lithium compounds in reaction of isocyanate and polyether polyol
US6590057B1 (en) 2001-08-29 2003-07-08 Bayer Aktiengesellschaft Polyurethane elastomers, process for their production and use thereof
WO2004113428A1 (en) * 2003-06-24 2004-12-29 Agro Biomass Consult Aps Method for mixing and homogenisation of binding agents and additives

Also Published As

Publication number Publication date
CA2361618A1 (en) 2000-08-10
EP1161498A1 (en) 2001-12-12
AU3008600A (en) 2000-08-25

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